{"meta":{"query_hash":"6e20af327332","filters":{"venue":"Nature Genetics"},"cohort_total":943,"direct_labels_cover":4,"predictions_cover":943,"exported":943,"export_cap":100000,"truncated":false,"label_status":"direct model label, unvalidated","prediction_status":"machine_predicted_unvalidated (Codex and Gemma teacher distillation)","score_status":"score_only:v0-immature-baseline","snapshot":{"source":"OpenAlex, pinned release, all 482 partitions","release":"2026-06-24","frame_built":"2026-07-12"},"permalink":"https://metacan.xera.ac/q/6e20af327332","api":"https://metacan.xera.ac/api/v1/cohort?venue=Nature+Genetics"},"results":[{"id":"W1235570584","doi":"10.1038/ng.467","title":"A genome-wide meta-analysis identifies 22 loci associated with eight hematological parameters in the HaemGen consortium","year":2009,"lang":"en","type":"article","venue":"Nature Genetics","topic":"T-cell and Retrovirus Studies","field":"Immunology and Microbiology","cited_by":22,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Ottawa","funders":"National Heart, Lung, and Blood Institute; Canadian Institutes of Health Research; National Center for Research Resources; Wellcome Trust","keywords":"Meta-analysis; Genetics; Biology; Genome; Computational biology; Medicine; Gene; Internal medicine","score_opus":0.02488339398618231,"score_gpt":0.25449528656875975,"score_spread":0.22961189258257744,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1235570584","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.994177,0.0013430382,0.0013574014,0.00018471161,0.000023279485,0.000010812315,0.0025669907,0.000054206597,0.00028269461],"genre_scores_gemma":[0.99557954,0.00031991894,0.0008225508,0.0000962055,0.000018458195,0.000020740741,0.0028219866,0.000048099657,0.00027246046],"study_design_codex":"observational","study_design_gemma":"meta_analysis","domain_scores_codex":[0.9971233,0.0010923046,0.00012721789,0.0009825488,0.00033051037,0.00034403324],"domain_scores_gemma":[0.99747604,0.0012601396,0.00031859314,0.0004807416,0.00018248356,0.00028195037],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.003903683,0.0012070513,0.0016436238,0.002543199,0.0009537198,0.0018436357,0.0012691047,0.0010659914,0.0016605043],"category_scores_gemma":[0.004165908,0.00053373404,0.0027201017,0.0036406121,0.0005251502,0.00034537815,0.001652365,0.0010435227,0.00021276194],"study_design_candidate":"meta_analysis","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0033765603,0.00009982454,0.9381818,0.00015895364,0.020332014,0.0010905315,0.00051584665,0.0019719463,0.018661246,0.0003106797,0.0018986055,0.013402074],"study_design_scores_gemma":[0.00024218198,0.00021062356,0.9796141,0.000054868302,0.011393502,0.0012256829,0.00042157166,0.0017641047,0.002433435,0.00040275438,0.0021829996,0.000054250897],"about_ca_topic_score_codex":0.0074417344,"about_ca_topic_score_gemma":0.00809435,"teacher_disagreement_score":0.0074417344,"about_ca_system_score_codex":0.0004095823,"about_ca_system_score_gemma":0.00077131303,"threshold_uncertainty_score":0.020644903},"labels":[],"label_agreement":null},{"id":"W1483951471","doi":"10.1038/ng.3289","title":"Mutations in XPR1 cause primary familial brain calcification associated with altered phosphate export","year":2015,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Parathyroid Disorders and Treatments","field":"Medicine","cited_by":316,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Toronto Western Hospital","funders":"National Institute of Neurological Disorders and Stroke; National Institute of Mental Health; National Heart, Lung, and Blood Institute; U.S. Public Health Service; Laboratoire d'Excellence EpiGenMed; Institut National de la Santé et de la Recherche Médicale; Institut National Du Cancer; University of California, Los Angeles; National Institutes of Health; Fondation pour la Recherche Médicale; Fundação de Amparo à Ciência e Tecnologia do Estado de Pernambuco; Agence Nationale de la Recherche; European Commission; Conselho Nacional de Desenvolvimento Científico e Tecnológico; Servicio Gallego de Salud; Instituto de Salud Carlos III; Women's Health Initiative","keywords":"PDGFRB; PDGFB; Biology; Nephrocalcinosis; Mutation; Calcification; Genetics; Gene; Internal medicine; Receptor; Medicine","score_opus":0.0275920716525454,"score_gpt":0.30729764333490894,"score_spread":0.27970557168236354,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1483951471","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9784419,0.004581209,0.0034818412,0.00292059,0.0003791613,0.000050710176,0.00069206284,0.0005381342,0.008914291],"genre_scores_gemma":[0.9962722,0.00052756164,0.0013055739,0.00023292212,0.00014368567,0.000008430334,0.00013235112,0.00006526923,0.0013119606],"study_design_codex":"case_report","study_design_gemma":"observational","domain_scores_codex":[0.99950874,0.00004467615,0.00007224114,0.00013109829,0.0001736724,0.000069590395],"domain_scores_gemma":[0.9988017,0.00040557573,0.00047600057,0.00006603538,0.00007701853,0.00017361129],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00029126924,0.002184436,0.0008530429,0.0013345465,0.00065628433,0.0007419993,0.001422378,0.004130032,0.0040337304],"category_scores_gemma":[0.0014999749,0.0005777918,0.00087090995,0.0010151966,0.0016547943,0.0004407136,0.000977362,0.001704931,0.00073004403],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00097198895,0.00016824176,0.015719784,0.00025041975,0.0003185361,0.77242756,0.00035517244,0.0006442004,0.19528103,0.0014677981,0.0022504863,0.010144792],"study_design_scores_gemma":[0.0003083844,0.00025915724,0.046124164,0.00009028253,0.00040708526,0.85619754,0.0002816725,0.0022208293,0.08661,0.0024353454,0.004978235,0.00008737924],"about_ca_topic_score_codex":0.0021270874,"about_ca_topic_score_gemma":0.0020653326,"teacher_disagreement_score":0.004130032,"about_ca_system_score_codex":0.0007983917,"about_ca_system_score_gemma":0.00056504324,"threshold_uncertainty_score":0.013494194},"labels":[],"label_agreement":null},{"id":"W1484977079","doi":"10.1038/75981","title":"Mutations of PKD1 in ADPKD2 cysts suggest a pathogenic effect of trans-heterozygous mutations","year":2000,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Genetic and Kidney Cyst Diseases","field":"Biochemistry, Genetics and Molecular Biology","cited_by":128,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"St. John’s Health Sciences Centre; Lunenfeld-Tanenbaum Research Institute; University Health Network","funders":"National Institute of Diabetes and Digestive and Kidney Diseases","keywords":"PKD1; Biology; Autosomal dominant polycystic kidney disease; Somatic cell; Genetics; Mutation; Cyst; Polycystic kidney disease; Gene; Kidney; Pathology","score_opus":0.0027272533792398685,"score_gpt":0.24319337391269802,"score_spread":0.24046612053345814,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1484977079","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9888821,0.0005896755,0.0040007327,0.00034075926,0.000078727986,0.000020259804,0.00031169015,0.00013855618,0.0056374758],"genre_scores_gemma":[0.9973514,0.00014546319,0.00133497,0.00005459007,0.000022265758,0.000009868862,0.00017551747,0.000041795945,0.00086409715],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9997588,0.00003364701,0.000036205816,0.000064885506,0.00007282998,0.000033676064],"domain_scores_gemma":[0.99938166,0.00021490775,0.00012583777,0.00006972843,0.000056154397,0.00015180798],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0002769592,0.0009896273,0.00046008808,0.00096388976,0.0006747398,0.0006524166,0.0005496143,0.0017005809,0.0048384615],"category_scores_gemma":[0.0010821125,0.00040665412,0.0004623457,0.00045467488,0.00091057864,0.00070799346,0.0006722542,0.0012150181,0.0014738005],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0010556744,0.00009242965,0.022561828,0.00019308542,0.00007099686,0.04300352,0.00028042658,0.00049541186,0.924309,0.0022845676,0.00041607284,0.0052369833],"study_design_scores_gemma":[0.00014877893,0.0003912814,0.045468967,0.000038899714,0.0001642513,0.23509875,0.00032517416,0.0037270328,0.70599973,0.0022850523,0.00628062,0.00007143244],"about_ca_topic_score_codex":0.0003152544,"about_ca_topic_score_gemma":0.00032177474,"teacher_disagreement_score":0.0048384615,"about_ca_system_score_codex":0.00025044451,"about_ca_system_score_gemma":0.00018377195,"threshold_uncertainty_score":0.016186297},"labels":[],"label_agreement":null},{"id":"W1485161311","doi":"10.1038/79216","title":"The common PPARγ Pro12Ala polymorphism is associated with decreased risk of type 2 diabetes","year":2000,"lang":"en","type":"review","venue":"Nature Genetics","topic":"Peroxisome Proliferator-Activated Receptors","field":"Biochemistry, Genetics and Molecular Biology","cited_by":1773,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"McGill Genome Centre; McGill University Health Centre","funders":"Wellcome Trust","keywords":"Type 2 diabetes; Population stratification; Biology; Odds ratio; Allele; Diabetes mellitus; Population; Case-control study; Peroxisome proliferator-activated receptor; Internal medicine; Genetics; Polymorphism (computer science); Allele frequency; Endocrinology; Genotype; Single-nucleotide polymorphism; Medicine; Receptor; Gene; Environmental health","score_opus":0.008651511194446432,"score_gpt":0.2648205905185894,"score_spread":0.256169079324143,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1485161311","genre_codex":"review","genre_gemma":"review","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"review","genre_consensus":"review","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.0016033733,0.9958897,0.00049787544,0.00068576797,0.00036445257,0.00000318895,0.00005494702,0.000013364139,0.00088729867],"genre_scores_gemma":[0.006514133,0.99073434,0.0005275995,0.00049426756,0.000667176,0.000007644546,0.00009209926,0.00000311522,0.000959678],"study_design_codex":"design_other","study_design_gemma":"observational","domain_scores_codex":[0.99984837,0.000025710397,0.000020773572,0.000048322025,0.00004577333,0.000011058632],"domain_scores_gemma":[0.9997142,0.00013977979,0.000063016065,0.000009683661,0.00005118198,0.000022178385],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0004443164,0.00086920016,0.0019268154,0.00078938785,0.00012475194,0.0005121903,0.00073274184,0.0010160359,0.001790413],"category_scores_gemma":[0.0005854478,0.00018203357,0.00031726246,0.0013037906,0.00026702724,0.00030983592,0.00026359168,0.00079905347,0.00088251714],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00080045016,0.0000690894,0.005072356,0.006363722,0.0005464706,0.001817814,0.00003254747,0.00028037198,0.004887977,0.0008230789,0.019228652,0.9600774],"study_design_scores_gemma":[0.0005158463,0.00065699464,0.057560835,0.0044095977,0.0028328465,0.021275304,0.00018323035,0.00039767765,0.0038111391,0.0049765175,0.9032882,0.00009168742],"about_ca_topic_score_codex":0.0012265589,"about_ca_topic_score_gemma":0.0015706394,"teacher_disagreement_score":0.0019268154,"about_ca_system_score_codex":0.000225417,"about_ca_system_score_gemma":0.00043772985,"threshold_uncertainty_score":0.005989492},"labels":[],"label_agreement":null},{"id":"W1485407919","doi":"10.1038/83817","title":"A 5-bp deletion in ELOVL4 is associated with two related forms of autosomal dominant macular dystrophy","year":2001,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Retinal Development and Disorders","field":"Biochemistry, Genetics and Molecular Biology","cited_by":457,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Alberta","funders":"National Eye Institute","keywords":"Macular dystrophy; Biology; Macular degeneration; Genetics; Dystrophy; Exon; Gene; Locus (genetics); Retinal degeneration; Ophthalmology; Medicine","score_opus":0.003063379132552032,"score_gpt":0.22428257033664853,"score_spread":0.2212191912040965,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1485407919","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9961039,0.00034930516,0.0014494425,0.00023973052,0.00007965858,0.00006034603,0.0003471338,0.00003953602,0.0013308979],"genre_scores_gemma":[0.9970372,0.00009072586,0.0009939212,0.00017535128,0.000056224922,0.000038195172,0.00041391412,0.000025804198,0.0011686763],"study_design_codex":"case_report","study_design_gemma":"observational","domain_scores_codex":[0.99934727,0.00013593037,0.00009725768,0.0001538427,0.00011064876,0.00015507592],"domain_scores_gemma":[0.99827325,0.00059571955,0.0005995925,0.000092148,0.00008609009,0.00035326296],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0004513302,0.0015958559,0.0008876362,0.0016025405,0.00070943777,0.00046671968,0.0011488271,0.0025958316,0.0026342084],"category_scores_gemma":[0.001927295,0.0004831886,0.001136765,0.00071486825,0.0014556589,0.00042825175,0.0013048751,0.0013121351,0.00083979877],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.007235755,0.0008683382,0.046296168,0.00033754305,0.00045346076,0.51508,0.001729377,0.0010605176,0.41245613,0.002289255,0.0011876712,0.011005774],"study_design_scores_gemma":[0.0010713304,0.0018978787,0.47465715,0.00016877186,0.0006316241,0.40747344,0.0013757318,0.0033238062,0.10039731,0.0021218606,0.0066450043,0.00023616936],"about_ca_topic_score_codex":0.001731556,"about_ca_topic_score_gemma":0.0012124405,"teacher_disagreement_score":0.0026342084,"about_ca_system_score_codex":0.0005828847,"about_ca_system_score_gemma":0.00029306562,"threshold_uncertainty_score":0.008812249},"labels":[],"label_agreement":null},{"id":"W1486948662","doi":"10.1038/74279","title":"The SH2 tyrosine phosphatase Shp2 is required for mammalian limb development","year":2000,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Protein Tyrosine Phosphatases","field":"Biochemistry, Genetics and Molecular Biology","cited_by":125,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Lunenfeld-Tanenbaum Research Institute; University of Toronto; Mount Sinai Hospital","funders":"","keywords":"Biology; Cell biology; Protein tyrosine phosphatase; Fibroblast growth factor; Limb bud; Receptor tyrosine kinase; Limb development; Mesoderm; Apical ectodermal ridge; Mutant; Signal transduction; Proto-oncogene tyrosine-protein kinase Src; Ectoderm; Morphogenesis; SH2 domain; Genetics; Receptor; Embryonic stem cell; Gene; Embryo; Embryogenesis","score_opus":0.008913320145284351,"score_gpt":0.258833816599193,"score_spread":0.24992049645390868,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1486948662","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.960582,0.0061086225,0.02177107,0.00072325644,0.00019367752,0.00004660854,0.0014809056,0.00068781804,0.008406132],"genre_scores_gemma":[0.9878362,0.001347135,0.0036441917,0.00011207705,0.000032108655,0.000022687944,0.0010741123,0.00011992585,0.005811521],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9998325,0.000012724152,0.000010832267,0.000033233748,0.00008014885,0.00003054072],"domain_scores_gemma":[0.99983704,0.00002581642,0.000044161236,0.000018190505,0.000017530278,0.00005721814],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00012981515,0.00050963456,0.00024237191,0.00036637206,0.000408472,0.00059896585,0.00032353948,0.00050142966,0.0013041191],"category_scores_gemma":[0.00020603667,0.00042746472,0.00021655767,0.00021271853,0.00046050758,0.00035838096,0.00054691965,0.0007997387,0.0007608569],"study_design_candidate":"bench_or_experimental","study_design_consensus":"bench_or_experimental","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00006209656,0.000004401036,0.00022401725,0.000022949824,0.0000038218673,0.0001618847,0.000006660181,0.000101178,0.9976835,0.00029934596,0.000114625305,0.0013155612],"study_design_scores_gemma":[0.000021573982,0.000034220677,0.01060185,0.0000059493614,0.000018159495,0.0011241006,0.000031244213,0.0018777869,0.9768891,0.0004040328,0.008982861,0.000009199817],"about_ca_topic_score_codex":0.0013034709,"about_ca_topic_score_gemma":0.003158896,"teacher_disagreement_score":0.0013041191,"about_ca_system_score_codex":0.0005736336,"about_ca_system_score_gemma":0.00032346766,"threshold_uncertainty_score":0.0043627024},"labels":[],"label_agreement":null},{"id":"W1487146757","doi":"10.1038/77076","title":"The glial cells missing-1 protein is essential for branching morphogenesis in the chorioallantoic placenta","year":2000,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Pregnancy and preeclampsia studies","field":"Medicine","cited_by":420,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Toronto; Mount Sinai Hospital; Lunenfeld-Tanenbaum Research Institute","funders":"","keywords":"Trophoblast; Biology; Chorioallantoic membrane; Placenta; Allantois; Cell biology; Placentation; Morphogenesis; Mesenchyme; Andrology; Embryo; Anatomy; Fetus; Genetics; Pregnancy; Medicine","score_opus":0.009243757473220404,"score_gpt":0.2698232748121297,"score_spread":0.2605795173389093,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1487146757","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9952245,0.0014693699,0.0018493736,0.00019376547,0.000033589124,0.000008844041,0.00017536397,0.0000412412,0.0010040306],"genre_scores_gemma":[0.99615115,0.0005375238,0.0012435463,0.000039991097,0.0000075073076,0.0000072300904,0.0002766099,0.000030307672,0.0017061558],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9997789,0.00004915302,0.00002088334,0.000043842105,0.00005947278,0.000047780748],"domain_scores_gemma":[0.9995303,0.000112046946,0.00016425569,0.000049441085,0.00003292139,0.000110989604],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00020579812,0.00033682867,0.00020009014,0.0006139521,0.00038642334,0.00042916776,0.0004066508,0.00045735322,0.0010000574],"category_scores_gemma":[0.00052603567,0.00026863033,0.00025001794,0.00022106431,0.00057107455,0.00021661633,0.00034864797,0.00077752565,0.00027718293],"study_design_candidate":"bench_or_experimental","study_design_consensus":"bench_or_experimental","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00034791155,0.000023728302,0.0016043632,0.0000330071,0.000013282866,0.0012435848,0.00005194593,0.0001407831,0.9944819,0.00048004673,0.000092492955,0.0014869523],"study_design_scores_gemma":[0.000072366216,0.000284721,0.050778966,0.000020436604,0.00010917526,0.008691785,0.00021739898,0.002383719,0.9310814,0.0007276306,0.005613966,0.000018267006],"about_ca_topic_score_codex":0.0015497316,"about_ca_topic_score_gemma":0.0012931068,"teacher_disagreement_score":0.0015497316,"about_ca_system_score_codex":0.00037490355,"about_ca_system_score_gemma":0.00039499,"threshold_uncertainty_score":0.0033454895},"labels":[],"label_agreement":null},{"id":"W1499352093","doi":"10.1038/ng782","title":"Deletion of Pten in mouse brain causes seizures, ataxia and defects in soma size resembling Lhermitte-Duclos disease","year":2001,"lang":"en","type":"article","venue":"Nature Genetics","topic":"PI3K/AKT/mTOR signaling in cancer","field":"Biochemistry, Genetics and Molecular Biology","cited_by":506,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"The Scarborough Hospital; Toronto Western Hospital; University of Toronto; University Health Network; Amgen (Canada); Ontario Institute for Cancer Research","funders":"","keywords":"Biology; Ataxia; PTEN; Soma; Disease; Genetics; Neuroscience; Pathology; Apoptosis; Medicine; PI3K/AKT/mTOR pathway","score_opus":0.009369481055000623,"score_gpt":0.27627156230662636,"score_spread":0.26690208125162573,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1499352093","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9789898,0.0018981658,0.010111185,0.0004240968,0.000074799405,0.000081984756,0.0025228953,0.000984793,0.0049123424],"genre_scores_gemma":[0.9829851,0.001620101,0.003944928,0.00007576023,0.000020454901,0.00009859404,0.0012132127,0.00017906872,0.009862612],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99973935,0.000029636818,0.000034393444,0.00006302967,0.00008235575,0.000051137893],"domain_scores_gemma":[0.99951136,0.0000684112,0.00022456211,0.000046439578,0.00002054206,0.00012872086],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00023795247,0.0013557889,0.00043109036,0.002220038,0.00042882815,0.00054765516,0.00051597785,0.00074551196,0.003549268],"category_scores_gemma":[0.00028090322,0.0006488273,0.00049722655,0.00076209597,0.0010475223,0.00060038245,0.00059837557,0.000994847,0.0012117738],"study_design_candidate":"bench_or_experimental","study_design_consensus":"bench_or_experimental","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00026764622,0.000042026248,0.0003998748,0.000051577295,0.000022615099,0.00096958707,0.00002773239,0.0001908645,0.9957072,0.00060989335,0.00013470913,0.0015762467],"study_design_scores_gemma":[0.00008232058,0.00023998902,0.0053258366,0.000011524218,0.00007111979,0.0031816885,0.00005736854,0.0010633541,0.98699397,0.0004661115,0.0024914627,0.000015283293],"about_ca_topic_score_codex":0.0014040011,"about_ca_topic_score_gemma":0.0032172643,"teacher_disagreement_score":0.003549268,"about_ca_system_score_codex":0.00045468897,"about_ca_system_score_gemma":0.00045226567,"threshold_uncertainty_score":0.011873543},"labels":[],"label_agreement":null},{"id":"W1501828520","doi":"10.1038/84853","title":"Regulation of glomerular basement membrane collagen expression by LMX1B contributes to renal disease in nail patella syndrome","year":2001,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Renal Diseases and Glomerulopathies","field":"Medicine","cited_by":210,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"SickKids Foundation; Hospital for Sick Children; University of Toronto","funders":"National Institute of Arthritis and Musculoskeletal and Skin Diseases; National Institute of Diabetes and Digestive and Kidney Diseases","keywords":"Biology; Alport syndrome; Type IV collagen; Collagen, type I, alpha 1; Molecular biology; Collagen VI; Cell biology; Endocrinology; Laminin; Extracellular matrix; Glomerulonephritis; Kidney","score_opus":0.006062423688756704,"score_gpt":0.2510327834922993,"score_spread":0.2449703598035426,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1501828520","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9959258,0.0008887299,0.0015947215,0.00027664413,0.000029002027,0.000008732129,0.000083159866,0.00006151521,0.0011316537],"genre_scores_gemma":[0.9981299,0.00020847355,0.0008131641,0.000084604246,0.000023935016,0.000009048513,0.000037402173,0.000026840786,0.00066667335],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9997701,0.00006501,0.000028909097,0.000045558445,0.000060144146,0.000030183483],"domain_scores_gemma":[0.99967635,0.00010783213,0.00012245624,0.00001864956,0.00001918205,0.000055437227],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00017304017,0.0005211612,0.00039192333,0.00058429444,0.00035396562,0.00032943962,0.00033048622,0.0005863824,0.002165959],"category_scores_gemma":[0.00047284746,0.00026099366,0.00022828019,0.00026692616,0.00048552567,0.00016252288,0.00033885197,0.00055374054,0.00029132506],"study_design_candidate":"bench_or_experimental","study_design_consensus":"bench_or_experimental","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0005645519,0.00005744596,0.012165109,0.00009337098,0.00004515827,0.016857646,0.000156651,0.00039758935,0.9631259,0.0008563783,0.00034824864,0.0053319656],"study_design_scores_gemma":[0.0003666195,0.00046589755,0.34865743,0.000104090504,0.0004179733,0.13938747,0.0005331836,0.010309884,0.49177468,0.0018842444,0.006029148,0.00006934465],"about_ca_topic_score_codex":0.0013603392,"about_ca_topic_score_gemma":0.0013274446,"teacher_disagreement_score":0.002165959,"about_ca_system_score_codex":0.00034473155,"about_ca_system_score_gemma":0.0001767711,"threshold_uncertainty_score":0.0072458982},"labels":[],"label_agreement":null},{"id":"W1503945760","doi":"10.1038/82508","title":"Genetic homogeneity of Icelanders","year":2000,"lang":"en","type":"letter","venue":"Nature Genetics","topic":"Nutrition, Genetics, and Disease","field":"Biochemistry, Genetics and Molecular Biology","cited_by":41,"is_retracted":false,"has_abstract":false,"route_ca_aff":false,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"","funders":"York University","keywords":"Biology; Homogeneity (statistics); Genetics; Evolutionary biology; Statistics","score_opus":0.005782807854810697,"score_gpt":0.23414372655412513,"score_spread":0.22836091869931444,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1503945760","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9355996,0.0029621366,0.0006429144,0.034596566,0.00092393346,0.000017077786,0.00067960256,0.000023175475,0.02455494],"genre_scores_gemma":[0.98167807,0.0016779536,0.00025392752,0.009082193,0.0008866323,0.0000112678745,0.00040641462,0.0000176202,0.0059859417],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99979824,0.000041493444,0.000010959777,0.000057187444,0.000032048214,0.00006005414],"domain_scores_gemma":[0.9996056,0.00011623692,0.00006609774,0.000044273496,0.00006901952,0.0000987807],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0007284387,0.00012286224,0.00025877357,0.00034521008,0.00058906985,0.0005932441,0.00019698395,0.0005299834,0.0019493641],"category_scores_gemma":[0.00076179457,0.00005506942,0.000101400896,0.0002835966,0.0006391168,0.0002574317,0.0004461352,0.00069575245,0.0002256802],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0070368196,0.00017720288,0.47447607,0.00025228673,0.00056210835,0.01105715,0.0074725216,0.0010215825,0.14352186,0.06931756,0.093587294,0.1915176],"study_design_scores_gemma":[0.000147511,0.00020340431,0.8230052,0.0001238263,0.00014631939,0.0039066854,0.0034225392,0.00035172107,0.011298467,0.009204698,0.14814435,0.00004529108],"about_ca_topic_score_codex":0.009953005,"about_ca_topic_score_gemma":0.014827477,"teacher_disagreement_score":0.009953005,"about_ca_system_score_codex":0.0007189223,"about_ca_system_score_gemma":0.0003241854,"threshold_uncertainty_score":0.019790113},"labels":[],"label_agreement":null},{"id":"W1507694958","doi":"10.1038/71626","title":"The Fanconi anaemia gene FANCF encodes a novel protein with homology to ROM","year":2000,"lang":"en","type":"article","venue":"Nature Genetics","topic":"DNA Repair Mechanisms","field":"Biochemistry, Genetics and Molecular Biology","cited_by":271,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Hospital for Sick Children; University of Toronto","funders":"National Heart, Lung, and Blood Institute","keywords":"Biology; Fanconi anemia; Genetics; Gene; Complementation; Homology (biology); DNA repair","score_opus":0.0040338566072613035,"score_gpt":0.22696980490217844,"score_spread":0.22293594829491714,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1507694958","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9671277,0.0046261624,0.019356668,0.00056560594,0.00023217978,0.000047413592,0.0008109135,0.0006105414,0.006622866],"genre_scores_gemma":[0.97756577,0.0009974783,0.00953723,0.000108967055,0.00009065817,0.00003024997,0.001345971,0.00004087157,0.010282861],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99993336,0.000005546801,0.0000033132267,0.000021888578,0.000019517554,0.0000162808],"domain_scores_gemma":[0.9998883,0.000027738946,0.000025345198,0.000008534778,0.000015039752,0.000035046858],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00012430154,0.00046826107,0.00026212932,0.00042365774,0.00037456912,0.0003905927,0.00037660182,0.0007099035,0.0012409006],"category_scores_gemma":[0.00023960185,0.00015548593,0.00031739497,0.0002412029,0.00032817008,0.00023043377,0.0002563462,0.00037261072,0.00066382857],"study_design_candidate":"bench_or_experimental","study_design_consensus":"bench_or_experimental","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00012258181,0.000028235498,0.00085289724,0.00006547736,0.000008615595,0.0023006483,0.000038628772,0.00024472203,0.9846572,0.0023384902,0.0006499245,0.008692643],"study_design_scores_gemma":[0.0000767648,0.000378848,0.024337675,0.000042765754,0.00005883113,0.024227642,0.00010224551,0.0032356274,0.8757926,0.0018739174,0.06981518,0.000057836463],"about_ca_topic_score_codex":0.00090335176,"about_ca_topic_score_gemma":0.00051932444,"teacher_disagreement_score":0.0012409006,"about_ca_system_score_codex":0.00036867344,"about_ca_system_score_gemma":0.00019163346,"threshold_uncertainty_score":0.004151225},"labels":[],"label_agreement":null},{"id":"W1508017125","doi":"10.1038/78071","title":"Human microphthalmia associated with mutations in the retinal homeobox gene CHX10","year":2000,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Ocular Disorders and Treatments","field":"Biochemistry, Genetics and Molecular Biology","cited_by":288,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"McGill University; Montreal Children's Hospital; University of Alberta; Lunenfeld-Tanenbaum Research Institute; Mount Sinai Hospital; University of Toronto; Hospital for Sick Children","funders":"","keywords":"Microphthalmia; Biology; Homeobox; Genetics; PAX6; Locus (genetics); Eye development; Anophthalmia; Phenotype; Gene; Molecular biology; Transcription factor","score_opus":0.004628751033422817,"score_gpt":0.24688907305192903,"score_spread":0.24226032201850622,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1508017125","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99082536,0.0012426872,0.0015732906,0.0002167414,0.00010387344,0.00004258971,0.00034056223,0.00008793759,0.0055670654],"genre_scores_gemma":[0.9974215,0.0003613659,0.00039719522,0.000061786464,0.000028826254,0.000010303275,0.00016317159,0.000013776659,0.0015421448],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99985015,0.000021990027,0.000012631135,0.0000319171,0.00005146379,0.000031794578],"domain_scores_gemma":[0.9998054,0.000057382123,0.00006193851,0.00001177485,0.000012975393,0.00005051322],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.000079550104,0.0006978964,0.00038890383,0.0007630996,0.00038831407,0.00021637937,0.00021195586,0.0006344344,0.003186263],"category_scores_gemma":[0.00026267947,0.0002003662,0.00029306783,0.000423662,0.00065716996,0.0001349436,0.00040826376,0.00050468795,0.00039653364],"study_design_candidate":"bench_or_experimental","study_design_consensus":"bench_or_experimental","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0019669968,0.00015638073,0.015948173,0.00018450912,0.00022423739,0.17521282,0.00031931512,0.0007842999,0.7828055,0.0025767228,0.0016694713,0.018151589],"study_design_scores_gemma":[0.00059272465,0.00136545,0.3247756,0.00011612634,0.0005606198,0.4005397,0.00044768752,0.0034832156,0.2532425,0.0024033086,0.012352385,0.00012064408],"about_ca_topic_score_codex":0.0031502978,"about_ca_topic_score_gemma":0.0039521623,"teacher_disagreement_score":0.003186263,"about_ca_system_score_codex":0.00047613628,"about_ca_system_score_gemma":0.00031621766,"threshold_uncertainty_score":0.010659099},"labels":[],"label_agreement":null},{"id":"W1508985588","doi":"10.1038/ng1001-229","title":"High-resolution haplotype structure in the human genome","year":2001,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Genetic Mapping and Diversity in Plants and Animals","field":"Biochemistry, Genetics and Molecular Biology","cited_by":1724,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"McGill Genome Centre","funders":"","keywords":"Haplotype; Biology; Linkage disequilibrium; Genetics; Haplotype estimation; Genome; Human genome; Single-nucleotide polymorphism; Population; Tag SNP; Genetic association; 1000 Genomes Project; Evolutionary biology; Computational biology; Allele; Gene; Genotype","score_opus":0.009221902563366403,"score_gpt":0.23622015515524797,"score_spread":0.22699825259188156,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1508985588","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99133205,0.0012957277,0.004146471,0.0002390907,0.000010093577,0.000008211539,0.0015404598,0.000037636113,0.0013901673],"genre_scores_gemma":[0.995812,0.00027742784,0.002230499,0.000059957703,0.000017825696,0.0000068754666,0.0011607951,0.000010371125,0.00042424258],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9998636,0.000046362384,0.0000067128585,0.000046870162,0.00001742261,0.000019060975],"domain_scores_gemma":[0.99937963,0.00029029828,0.00010739767,0.000093680705,0.00005529497,0.0000737439],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0002888462,0.000076379256,0.00025040295,0.0008323796,0.00032259885,0.00041146154,0.00016826067,0.00036511495,0.0010489768],"category_scores_gemma":[0.0010100886,0.00022425636,0.00016329864,0.0012007613,0.0002811768,0.00025611508,0.00021477057,0.0005107864,0.0002819174],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0025152767,0.00018897778,0.5448575,0.0004672867,0.000881398,0.004416587,0.002870307,0.0323943,0.22893377,0.02059111,0.0067459526,0.15513757],"study_design_scores_gemma":[0.00015609061,0.00017805143,0.94729406,0.000078319215,0.00028878395,0.0027105685,0.0003434857,0.010546674,0.008175944,0.020756654,0.009424406,0.00004696001],"about_ca_topic_score_codex":0.0025482206,"about_ca_topic_score_gemma":0.005181711,"teacher_disagreement_score":0.0025482206,"about_ca_system_score_codex":0.00018108351,"about_ca_system_score_gemma":0.00027205862,"threshold_uncertainty_score":0.0050667524},"labels":[],"label_agreement":null},{"id":"W1516387975","doi":"10.1038/85808","title":"Selection for transgene homozygosity in embryonic stem cells results in extensive loss of heterozygosity","year":2001,"lang":"en","type":"article","venue":"Nature Genetics","topic":"CRISPR and Genetic Engineering","field":"Biochemistry, Genetics and Molecular Biology","cited_by":43,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Lunenfeld-Tanenbaum Research Institute; University of Toronto; Mount Sinai Hospital","funders":"","keywords":"Biology; Loss of heterozygosity; Embryonic stem cell; Mutagenesis; Genetics; Transgene; Stem cell; Genome; Gene; Mutation; Cell biology; Allele","score_opus":0.007139536462912204,"score_gpt":0.2791786279113108,"score_spread":0.2720390914483986,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1516387975","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.92786217,0.0007390368,0.061429095,0.00039091616,0.00014560155,0.00013836988,0.0015230547,0.0018011286,0.0059707277],"genre_scores_gemma":[0.9750729,0.0005701715,0.013447723,0.00024630775,0.00002260304,0.00010145052,0.0013657566,0.00077109813,0.008401966],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9992705,0.00009497332,0.00009126451,0.00014392263,0.00030618376,0.00009322594],"domain_scores_gemma":[0.9990227,0.00035858504,0.00023135007,0.00014045963,0.000060200262,0.00018664196],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.000653115,0.000676202,0.00083849655,0.00079984305,0.00033390464,0.0007045282,0.00050688616,0.0007099001,0.0033575483],"category_scores_gemma":[0.0004497986,0.0005366407,0.0005210273,0.0004882621,0.0007471884,0.0003093651,0.00096082425,0.0013119939,0.0021866914],"study_design_candidate":"bench_or_experimental","study_design_consensus":"bench_or_experimental","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.000024870893,0.000011922617,0.00013578199,0.000014499594,0.000008279264,0.00015777987,0.000011627397,0.00005699561,0.99820304,0.00023347727,0.00006466837,0.0010770427],"study_design_scores_gemma":[0.000028172777,0.00006136675,0.0036653427,0.000009633481,0.000028070732,0.00135092,0.00002690366,0.00087678974,0.9905071,0.00023812246,0.0031898909,0.000017594752],"about_ca_topic_score_codex":0.00041109184,"about_ca_topic_score_gemma":0.0015756493,"teacher_disagreement_score":0.0033575483,"about_ca_system_score_codex":0.00029041298,"about_ca_system_score_gemma":0.0004073047,"threshold_uncertainty_score":0.011232138},"labels":[],"label_agreement":null},{"id":"W1517532080","doi":"10.1038/71743","title":"Molecular mechanism for duplication 17p11.2— the homologous recombination reciprocal of the Smith-Magenis microdeletion","year":2000,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Genomic variations and chromosomal abnormalities","field":"Biochemistry, Genetics and Molecular Biology","cited_by":424,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"North York General Hospital","funders":"Eunice Kennedy Shriver National Institute of Child Health and Human Development; National Cancer Institute","keywords":"Gene duplication; Non-allelic homologous recombination; Biology; Genetics; Homologous recombination; Recombination; Homologous chromosome; Tandem exon duplication; Ectopic recombination; Gene; Gene rearrangement; Chromosomal inversion; Chromosome; Genetic recombination; Karyotype","score_opus":0.004171553387211045,"score_gpt":0.21565615398237767,"score_spread":0.21148460059516663,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1517532080","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99056,0.0024319864,0.0039656092,0.00038811806,0.000043859767,0.00008180731,0.00035033945,0.00014428473,0.002033989],"genre_scores_gemma":[0.9957847,0.0010443622,0.0015877294,0.00006554085,0.000057602134,0.00006523431,0.00038539225,0.000010789935,0.0009986822],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.99981695,0.000025156192,0.000018155097,0.00006616589,0.000040327734,0.000033338747],"domain_scores_gemma":[0.99986756,0.000033695276,0.000045549943,0.000015487865,0.000009707756,0.00002804394],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00012510037,0.0006134669,0.00039302872,0.0007812774,0.00034654225,0.00028444175,0.00056988455,0.0008107859,0.0025720175],"category_scores_gemma":[0.0004174835,0.00036151853,0.00031789014,0.00029638095,0.0006958373,0.0003080795,0.0004019057,0.0005211281,0.0008323943],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00079372927,0.00020907048,0.069903225,0.00035110317,0.00010258938,0.12457576,0.0008046172,0.0011988477,0.7648309,0.0076150973,0.0011944431,0.028420616],"study_design_scores_gemma":[0.00038671083,0.0010277282,0.1694426,0.00015829089,0.00021521706,0.54735917,0.0005818791,0.0032913347,0.2546949,0.0033858318,0.019374205,0.000082088045],"about_ca_topic_score_codex":0.0004606768,"about_ca_topic_score_gemma":0.00019791661,"teacher_disagreement_score":0.0025720175,"about_ca_system_score_codex":0.00040299393,"about_ca_system_score_gemma":0.00032587422,"threshold_uncertainty_score":0.008604288},"labels":[],"label_agreement":null},{"id":"W1518382324","doi":"10.1038/79201","title":"Mutations in MKKS cause obesity, retinal dystrophy and renal malformations associated with Bardet-Biedl syndrome","year":2000,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Genetic and Kidney Cyst Diseases","field":"Biochemistry, Genetics and Molecular Biology","cited_by":321,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Simon Fraser University; Memorial University of Newfoundland","funders":"National Eye Institute","keywords":"Bardet–Biedl syndrome; Polydactyly; Biology; Genetics; Frameshift mutation; Gene; Mutation","score_opus":0.003760634257528809,"score_gpt":0.21781812005102288,"score_spread":0.21405748579349407,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1518382324","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9946227,0.0009442963,0.0015088381,0.00034563956,0.000055118857,0.000018992298,0.0003576629,0.00014491007,0.0020018225],"genre_scores_gemma":[0.99801886,0.00021908105,0.0010497258,0.00006352777,0.000036366713,0.000007778104,0.00010617259,0.000019452486,0.00047899346],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.99975747,0.000026605801,0.000034573102,0.00004601408,0.00009257784,0.000042740314],"domain_scores_gemma":[0.99947256,0.00013292073,0.00020210452,0.00001881027,0.000025044708,0.00014864058],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00018657857,0.0012039653,0.00036913328,0.0013842547,0.00042913688,0.00036047405,0.00042747147,0.0013025656,0.0015405721],"category_scores_gemma":[0.00080592156,0.00038290466,0.00028830062,0.0007821188,0.0008322285,0.0003118633,0.00066909153,0.00059166073,0.0005218123],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0028568744,0.00024188677,0.07298593,0.00038373063,0.000354859,0.33525008,0.001059497,0.0018316945,0.55365485,0.0043372856,0.0034684385,0.023574848],"study_design_scores_gemma":[0.0005468057,0.00038603018,0.36739475,0.000103712504,0.000473396,0.531273,0.00046443942,0.0053093764,0.0819755,0.0035183143,0.008406071,0.00014866788],"about_ca_topic_score_codex":0.0012741224,"about_ca_topic_score_gemma":0.0018011618,"teacher_disagreement_score":0.0015405721,"about_ca_system_score_codex":0.00035741468,"about_ca_system_score_gemma":0.00024109508,"threshold_uncertainty_score":0.0051537156},"labels":[],"label_agreement":null},{"id":"W1525509607","doi":"10.1038/90054","title":"Fusion of two novel genes, RBM15 and MKL1, in the t(1;22)(p13;q13) of acute megakaryoblastic leukemia","year":2001,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Plant Disease Resistance and Genetics","field":"Agricultural and Biological Sciences","cited_by":303,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"SickKids Foundation; Hospital for Sick Children; University of Toronto","funders":"National Cancer Institute","keywords":"Acute megakaryoblastic leukemia; Biology; Gene; Chromosomal translocation; Fusion protein; Fusion gene; Acute myelomonocytic leukemia; Molecular biology; Genetics; Cancer research; Leukemia; Recombinant DNA","score_opus":0.009817083470923487,"score_gpt":0.23506002848200003,"score_spread":0.22524294501107653,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1525509607","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99461657,0.00067131966,0.0026632282,0.0003503598,0.00005523692,0.00003691142,0.00027134427,0.000105871506,0.0012291985],"genre_scores_gemma":[0.9975867,0.00012300306,0.0011350799,0.00008598799,0.000012734932,0.000012573921,0.00018815602,0.000023270431,0.0008324475],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99973613,0.00003197878,0.00005012449,0.000057994628,0.000065083776,0.000058582864],"domain_scores_gemma":[0.9995912,0.00010542572,0.00011675786,0.000037143505,0.000018519691,0.00013105922],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0002521105,0.00039256984,0.00050615805,0.00062552554,0.00053427863,0.0006850209,0.0007412032,0.00172586,0.0016381284],"category_scores_gemma":[0.0005955892,0.0003857803,0.000526295,0.0005606421,0.0007985998,0.00035207978,0.00078132696,0.00090873765,0.000724006],"study_design_candidate":"bench_or_experimental","study_design_consensus":"bench_or_experimental","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0018808353,0.00016227689,0.010044145,0.00017580469,0.0000870806,0.12910132,0.00053792796,0.002203587,0.8368514,0.00379858,0.0010491112,0.01410788],"study_design_scores_gemma":[0.00061715965,0.0007606016,0.09739412,0.000072788804,0.000491725,0.3103929,0.00061030587,0.009157492,0.56237024,0.003409949,0.014618232,0.00010451253],"about_ca_topic_score_codex":0.0009294336,"about_ca_topic_score_gemma":0.0011007577,"teacher_disagreement_score":0.00172586,"about_ca_system_score_codex":0.001023234,"about_ca_system_score_gemma":0.00037677021,"threshold_uncertainty_score":0.007424116},"labels":[],"label_agreement":null},{"id":"W1526637642","doi":"10.1038/77004","title":"ABCR expression in foveal cone photoreceptors and its role in Stargardt macular dystrophy","year":2000,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Retinal Development and Disorders","field":"Biochemistry, Genetics and Molecular Biology","cited_by":270,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of British Columbia","funders":"","keywords":"Foveal; Stargardt disease; Biology; ABCA4; Macular dystrophy; Genetics; Gene; Ophthalmology; Retinal; Phenotype; Botany; Medicine","score_opus":0.002526372528965446,"score_gpt":0.21453506706904257,"score_spread":0.21200869454007712,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1526637642","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9947626,0.0030242,0.00074573176,0.00019263754,0.000012476182,0.0000047923268,0.000089360954,0.000020116448,0.0011481897],"genre_scores_gemma":[0.9974986,0.00055327965,0.00049557444,0.000041397136,0.000012508229,0.0000052332757,0.000076212185,0.000007945445,0.0013092589],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99979764,0.000040318493,0.000028249813,0.000035200574,0.000053010448,0.00004560078],"domain_scores_gemma":[0.9998135,0.00004987583,0.000039935152,0.000021841875,0.000036489273,0.000038356175],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0002916338,0.00012460916,0.00028877708,0.00077521073,0.00040801804,0.00061081466,0.00023934341,0.0005022881,0.0007781813],"category_scores_gemma":[0.00045283942,0.00021257093,0.00022143181,0.00028357308,0.000566597,0.0003972004,0.00022910158,0.00036127167,0.00024451612],"study_design_candidate":"bench_or_experimental","study_design_consensus":"bench_or_experimental","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0006133506,0.00003609521,0.0032302893,0.000060971193,0.000012244758,0.00127579,0.0001087374,0.00022236312,0.98964256,0.0013668537,0.00013882175,0.0032919096],"study_design_scores_gemma":[0.00018125892,0.00063029415,0.22915715,0.00003856686,0.00013944853,0.016869212,0.0012035951,0.006940695,0.73260385,0.0025601946,0.009619834,0.00005588076],"about_ca_topic_score_codex":0.0027355186,"about_ca_topic_score_gemma":0.0017443382,"teacher_disagreement_score":0.0027355186,"about_ca_system_score_codex":0.00059486675,"about_ca_system_score_gemma":0.00019761492,"threshold_uncertainty_score":0.0054391623},"labels":[],"label_agreement":null},{"id":"W1536408199","doi":"10.1038/ng703","title":"Mutations in the gene encoding immunoglobulin μ-binding protein 2 cause spinal muscular atrophy with respiratory distress type 1","year":2001,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Neurogenetic and Muscular Disorders Research","field":"Medicine","cited_by":344,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Alberta Children's Hospital; University of Calgary","funders":"","keywords":"Spinal muscular atrophy; SMN1; Biology; Exon; Genetics; Frameshift mutation; RNA splicing; Gene; Molecular biology; RNA","score_opus":0.025757527002387905,"score_gpt":0.32154226668883906,"score_spread":0.29578473968645114,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1536408199","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9928027,0.0013630149,0.001164283,0.00082363107,0.0002272851,0.00004640006,0.00036134233,0.00011554543,0.0030958282],"genre_scores_gemma":[0.9972646,0.00029771737,0.0006056002,0.00020723873,0.00011495434,0.000013146094,0.00017775345,0.000022874845,0.0012961689],"study_design_codex":"case_report","study_design_gemma":"observational","domain_scores_codex":[0.9997547,0.00002662918,0.000021566346,0.00006430483,0.00008168027,0.000051124345],"domain_scores_gemma":[0.99962294,0.00011943739,0.00010350679,0.00001273729,0.000024176434,0.00011708784],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00016008952,0.0017060555,0.00055543915,0.0009349359,0.0006994525,0.00041471858,0.00068877474,0.0020201816,0.0019308461],"category_scores_gemma":[0.0012367913,0.00031789226,0.00044486354,0.00067355984,0.0007971252,0.00027947538,0.0004917113,0.0010646969,0.0005593339],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.001084473,0.00030660315,0.0633388,0.00028392443,0.00026481468,0.60998505,0.0009660457,0.0009571773,0.2967505,0.0012419785,0.004595678,0.02022501],"study_design_scores_gemma":[0.00033734652,0.0007998684,0.267521,0.00010652449,0.00043056594,0.6783086,0.000638559,0.0024023906,0.038566533,0.0010232098,0.009766231,0.00009919747],"about_ca_topic_score_codex":0.0022071283,"about_ca_topic_score_gemma":0.002052572,"teacher_disagreement_score":0.0022071283,"about_ca_system_score_codex":0.00056808785,"about_ca_system_score_gemma":0.0002815953,"threshold_uncertainty_score":0.0064592957},"labels":[],"label_agreement":null},{"id":"W1537435549","doi":"10.1038/ng.3302","title":"PDE3A mutations cause autosomal dominant hypertension with brachydactyly","year":2015,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Phosphodiesterase function and regulation","field":"Biochemistry, Genetics and Molecular Biology","cited_by":171,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Hospital for Sick Children; University of Toronto; SickKids Foundation; Mount Sinai Hospital","funders":"Deutsche Hochdruckliga; Deutsche Stiftung für Herzforschung; U.S. Department of Veterans Affairs; Else Kröner-Fresenius-Stiftung; Deutsche Forschungsgemeinschaft; American Heart Association; University of Utah","keywords":"Brachydactyly; Biology; Internal medicine; Endocrinology; Missense mutation; Mutation; Genetics; Medicine; Gene","score_opus":0.01302358554171426,"score_gpt":0.2480162320357023,"score_spread":0.23499264649398804,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1537435549","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.97977406,0.0017200233,0.0061416235,0.0016254428,0.0004235175,0.000087268796,0.0022206365,0.00048351602,0.0075239455],"genre_scores_gemma":[0.99469984,0.0004330836,0.0025489687,0.00027928344,0.0001137904,0.000019154155,0.00025771922,0.00008907642,0.0015591047],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9995821,0.000036275305,0.000051243005,0.00012226269,0.0001382129,0.000069856236],"domain_scores_gemma":[0.9993943,0.00015063325,0.00021907836,0.000024613455,0.000021018799,0.00019041645],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00019626666,0.0017694042,0.0006055803,0.0012368301,0.00064196624,0.0004717532,0.0008516533,0.0018541754,0.0032427933],"category_scores_gemma":[0.0008180747,0.00048138006,0.00095550565,0.00084237376,0.001480654,0.00026803627,0.0009191726,0.0012694703,0.0004793356],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0006706622,0.00009461412,0.019286169,0.0001810694,0.00032624364,0.44377276,0.0003776442,0.0008292641,0.5225094,0.0024567978,0.0023281544,0.0071672066],"study_design_scores_gemma":[0.0005769397,0.000289617,0.21566828,0.00011414263,0.00072088686,0.6880832,0.00029433772,0.0034842263,0.07722299,0.0028957888,0.010457235,0.00019239861],"about_ca_topic_score_codex":0.004329341,"about_ca_topic_score_gemma":0.0074771475,"teacher_disagreement_score":0.004329341,"about_ca_system_score_codex":0.0006589872,"about_ca_system_score_gemma":0.00071750616,"threshold_uncertainty_score":0.010848224},"labels":[],"label_agreement":null},{"id":"W1543309406","doi":"10.1038/ng0610-472","title":"Reply to “Reassessing evidence for a postnatal mitochondrial genetic bottleneck”","year":2010,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Mitochondrial Function and Pathology","field":"Biochemistry, Genetics and Molecular Biology","cited_by":3,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"McGill University; Montreal Neurological Institute and Hospital","funders":"","keywords":"Biology; Bottleneck; Genetics; Mitochondrial DNA; Evolutionary biology; Population bottleneck; Gene; Allele","score_opus":0.017360046144737733,"score_gpt":0.3140299189922709,"score_spread":0.29666987284753316,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1543309406","genre_codex":"commentary","genre_gemma":"commentary","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"commentary","genre_consensus":"commentary","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.0004704868,0.0026997013,0.00037722994,0.9237669,0.0721014,0.000006468737,0.000093445975,0.00005721162,0.00042718023],"genre_scores_gemma":[0.0032796802,0.001221947,0.0003431897,0.9355624,0.057906955,0.00002652494,0.00006189317,0.00003673083,0.0015607983],"study_design_codex":"not_applicable","study_design_gemma":"not_applicable","domain_scores_codex":[0.9973041,0.0005850451,0.00044652217,0.00061956287,0.000554044,0.00049078435],"domain_scores_gemma":[0.97643626,0.0132106505,0.0020927119,0.0014189979,0.004335778,0.0025054996],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0060785883,0.0012050075,0.0019290652,0.0012037565,0.0038778326,0.0028184685,0.004325035,0.04709923,0.005559948],"category_scores_gemma":[0.047531713,0.0012703339,0.0017668717,0.0010518989,0.0056676613,0.004316983,0.0046135015,0.05629005,0.005212668],"study_design_candidate":"not_applicable","study_design_consensus":"not_applicable","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00013928153,0.000018808172,0.0008582683,0.00015974067,0.00006619731,0.0012628685,0.00024312659,0.00008607983,0.0007689825,0.00176524,0.98741025,0.0072212014],"study_design_scores_gemma":[0.00016808865,0.00010642326,0.0037556763,0.0005809828,0.00021078579,0.00309366,0.000868627,0.0003472772,0.001703711,0.01040923,0.9786012,0.00015430863],"about_ca_topic_score_codex":0.0029861236,"about_ca_topic_score_gemma":0.0031995163,"teacher_disagreement_score":0.04709923,"about_ca_system_score_codex":0.0024389394,"about_ca_system_score_gemma":0.0026973893,"threshold_uncertainty_score":0.03214699},"labels":[],"label_agreement":null},{"id":"W1546537221","doi":"10.1038/ng575","title":"Aromatic hydrocarbon receptor-driven Bax gene expression is required for premature ovarian failure caused by biohazardous environmental chemicals","year":2001,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Toxic Organic Pollutants Impact","field":"Environmental Science","cited_by":465,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Lunenfeld-Tanenbaum Research Institute; Mount Sinai Hospital","funders":"National Institute of Environmental Health Sciences","keywords":"Aryl hydrocarbon receptor; Toxicant; Apoptosis; Biology; Polycyclic aromatic hydrocarbon; Oocyte; Aryl hydrocarbon receptor nuclear translocator; Transcription (linguistics); Transcription factor; Cell biology; Gene; Internal medicine; Toxicity; Genetics; Medicine; Embryo","score_opus":0.006290256576393204,"score_gpt":0.22395054889243898,"score_spread":0.21766029231604578,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1546537221","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99768686,0.00038286054,0.0010435659,0.00011529995,0.000031290157,0.000013647421,0.00020181637,0.000051959203,0.0004727052],"genre_scores_gemma":[0.9985911,0.00016005767,0.00041528352,0.000025890819,0.000006738988,0.00001358903,0.00016637001,0.000017841503,0.0006031117],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99968624,0.000083451254,0.000039486553,0.000045546287,0.000076511074,0.00006880564],"domain_scores_gemma":[0.9990269,0.00034950877,0.0003052288,0.0001343972,0.00004320189,0.00014075024],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00021827452,0.00023044739,0.00030517724,0.00048541994,0.00026022168,0.00024165452,0.0003104669,0.00040636075,0.0023041845],"category_scores_gemma":[0.00062965206,0.00029470527,0.00037511054,0.00017060839,0.00061154977,0.00018457025,0.00042760654,0.0006509384,0.00045192862],"study_design_candidate":"bench_or_experimental","study_design_consensus":"bench_or_experimental","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0006318475,0.000044857577,0.0013209478,0.000027427188,0.0000091707725,0.0012155994,0.000021755994,0.00008776534,0.99553657,0.00018468659,0.000071708804,0.0008477381],"study_design_scores_gemma":[0.00015882587,0.00047897352,0.04822127,0.000013402766,0.00004485284,0.009877936,0.00015802117,0.0023519897,0.93613404,0.0004546358,0.0020831295,0.00002291121],"about_ca_topic_score_codex":0.0002950713,"about_ca_topic_score_gemma":0.00042726327,"teacher_disagreement_score":0.0023041845,"about_ca_system_score_codex":0.00025489874,"about_ca_system_score_gemma":0.00020528366,"threshold_uncertainty_score":0.007708311},"labels":[],"label_agreement":null},{"id":"W1547443377","doi":"10.1038/84808","title":"A candidate prostate cancer susceptibility gene at chromosome 17p","year":2001,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Forensic and Genetic Research","field":"Biochemistry, Genetics and Molecular Biology","cited_by":555,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"SickKids Foundation; University of Toronto; Hospital for Sick Children; Université Laval","funders":"National Cancer Institute; University of Utah","keywords":"Biology; Genetics; Gene; Frameshift mutation; Locus (genetics); Missense mutation; Positional cloning; Mutation","score_opus":0.007991403816154602,"score_gpt":0.29673456151413274,"score_spread":0.28874315769797815,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1547443377","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9906715,0.0013714063,0.0024999818,0.0012092857,0.00018954783,0.000038781076,0.00090402266,0.00015815037,0.0029572726],"genre_scores_gemma":[0.99293256,0.0005716585,0.0019993978,0.00017796822,0.000110626665,0.000026886895,0.0008751111,0.000029179744,0.0032765584],"study_design_codex":"case_report","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9998511,0.000022892893,0.000008226576,0.000044867742,0.0000325323,0.000040399784],"domain_scores_gemma":[0.99917346,0.00039035885,0.0001870178,0.000035144363,0.000050540304,0.00016353164],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00020931193,0.0007926993,0.0006239759,0.002331544,0.000759553,0.00048382094,0.0010853088,0.0015208046,0.010086334],"category_scores_gemma":[0.0011381838,0.00041819806,0.0006828233,0.0012567431,0.00074225885,0.00020583856,0.00047795498,0.00081953057,0.0009163683],"study_design_candidate":"bench_or_experimental","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.006525025,0.00059479283,0.1775235,0.0006870275,0.0008473049,0.37606698,0.0013423486,0.0017704391,0.3718899,0.00863309,0.0039319536,0.050187636],"study_design_scores_gemma":[0.0016338633,0.0019063344,0.4813531,0.00033132857,0.0022065435,0.3089721,0.0016096758,0.0050685247,0.1485001,0.009219414,0.039050654,0.0001483011],"about_ca_topic_score_codex":0.0020233372,"about_ca_topic_score_gemma":0.0018203745,"teacher_disagreement_score":0.010086334,"about_ca_system_score_codex":0.0004159773,"about_ca_system_score_gemma":0.0005253672,"threshold_uncertainty_score":0.03374213},"labels":[],"label_agreement":null},{"id":"W1549194503","doi":"10.1038/81691","title":"A common variant in BRCA2 is associated with both breast cancer risk and prenatal viability","year":2000,"lang":"en","type":"article","venue":"Nature Genetics","topic":"BRCA gene mutations in cancer","field":"Biochemistry, Genetics and Molecular Biology","cited_by":171,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Children's & Women's Health Centre of British Columbia","funders":"Wellcome Trust","keywords":"Biology; Breast cancer; Penetrance; Allele; Genetics; BRCA2 Protein; Cancer; Internal medicine; Exon; Oncology; Gene; Mutation; Phenotype; Germline mutation; Medicine","score_opus":0.003505751064878523,"score_gpt":0.24338983848450346,"score_spread":0.23988408741962494,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1549194503","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9908681,0.0013873146,0.0022961795,0.000743954,0.00016259028,0.0000396598,0.0018134582,0.0001306168,0.0025581822],"genre_scores_gemma":[0.99634665,0.00026161261,0.0010679843,0.00013172158,0.00012730177,0.000019048059,0.0005427575,0.000037337344,0.0014656683],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99928373,0.00013129372,0.000078586054,0.00022290683,0.00019928429,0.00008416352],"domain_scores_gemma":[0.99778867,0.00094281416,0.0006500252,0.00013205368,0.00013189335,0.00035456038],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00035865695,0.0017925305,0.0008372375,0.002774837,0.0010122928,0.0005174744,0.0009865034,0.0023525378,0.007156444],"category_scores_gemma":[0.0030735459,0.00041427012,0.0008914571,0.0019405708,0.00077742455,0.00040654017,0.0006258785,0.0011257243,0.00069697027],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.005071864,0.00059866917,0.36363056,0.0003668257,0.0010366291,0.2832519,0.0015986634,0.0011371655,0.3083824,0.0033302358,0.0038971012,0.027697952],"study_design_scores_gemma":[0.0002697178,0.000856061,0.5662929,0.00015392536,0.0007035469,0.3841883,0.00051574357,0.0020283312,0.03514748,0.002122115,0.007580791,0.00014109128],"about_ca_topic_score_codex":0.0026586473,"about_ca_topic_score_gemma":0.0019171662,"teacher_disagreement_score":0.007156444,"about_ca_system_score_codex":0.00026223832,"about_ca_system_score_gemma":0.0003278136,"threshold_uncertainty_score":0.023940623},"labels":[],"label_agreement":null},{"id":"W1549619413","doi":"10.1038/ng.3315","title":"Spatial genomic heterogeneity within localized, multifocal prostate cancer","year":2015,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Prostate Cancer Treatment and Research","field":"Medicine","cited_by":489,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of British Columbia; Genome British Columbia; Université Laval; University of Toronto; University Health Network; Toronto General Hospital; BC Cancer Agency; Simon Fraser University; Princess Margaret Cancer Centre; Ontario Institute for Cancer Research","funders":"Canadian Institutes of Health Research; Cancer Research UK","keywords":"Biology; Prostate cancer; Genomics; Cancer; Genetic heterogeneity; Prostate; Computational biology; Tumor heterogeneity; Genome; Single-nucleotide polymorphism; Genetics; Gene; Genotype; Phenotype","score_opus":0.03187420802986779,"score_gpt":0.3501329320635392,"score_spread":0.3182587240336714,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1549619413","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99482924,0.0013157667,0.00251181,0.00015954733,0.000006691982,0.000005963887,0.00020808539,0.0000570993,0.00090575643],"genre_scores_gemma":[0.9994199,0.00008470171,0.00026442634,0.000017943132,0.0000067902874,0.0000025755137,0.000060482744,0.000007925079,0.00013517906],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99964535,0.000054680157,0.00001310144,0.0001244209,0.000084434156,0.00007790889],"domain_scores_gemma":[0.99917275,0.00026202988,0.00027651913,0.00011845387,0.000079163714,0.000091003465],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00031515706,0.00012336529,0.00033674552,0.0010533736,0.00024334699,0.0005387042,0.00033358904,0.00030208705,0.0021288553],"category_scores_gemma":[0.0017414229,0.0003244572,0.00024597874,0.0007623753,0.0005288591,0.0004631785,0.00057246035,0.00031336627,0.00019146854],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0018813587,0.000098081764,0.5211191,0.0003776151,0.00062432885,0.002111138,0.001220762,0.012078436,0.38930893,0.0053075547,0.0015402457,0.06433239],"study_design_scores_gemma":[0.00003049033,0.00012505469,0.97348976,0.000015396761,0.00015213313,0.0030835283,0.0006256251,0.0053192335,0.0110709835,0.0043464256,0.0017089437,0.000032471584],"about_ca_topic_score_codex":0.0032868406,"about_ca_topic_score_gemma":0.005126445,"teacher_disagreement_score":0.0032868406,"about_ca_system_score_codex":0.0004271729,"about_ca_system_score_gemma":0.00022999675,"threshold_uncertainty_score":0.0071218014},"labels":[],"label_agreement":null},{"id":"W1550555606","doi":"10.1038/ng835","title":"Hermansky-Pudlak syndrome is caused by mutations in HPS4, the human homolog of the mouse light-ear gene","year":2002,"lang":"en","type":"article","venue":"Nature Genetics","topic":"melanin and skin pigmentation","field":"Biochemistry, Genetics and Molecular Biology","cited_by":182,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Hospital for Sick Children","funders":"","keywords":"Biology; Hermansky–Pudlak syndrome; Melanosome; Phenotype; Oculocutaneous albinism; Mutant; Genetics; Locus (genetics); Molecular biology; Gene; Pathology; Pulmonary fibrosis; Melanin; Medicine; Fibrosis","score_opus":0.007840742985959449,"score_gpt":0.24472967949933055,"score_spread":0.23688893651337112,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1550555606","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9896472,0.0010997378,0.0032529666,0.00028614735,0.0001173133,0.000056661527,0.0005453924,0.0003925902,0.0046020774],"genre_scores_gemma":[0.9933083,0.00048542445,0.0016327611,0.000057730056,0.000057850037,0.00002797541,0.00020317432,0.00004241005,0.004184361],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99977785,0.000030832067,0.000018802739,0.00005056326,0.00008864451,0.000033204942],"domain_scores_gemma":[0.9997329,0.000054372722,0.00010914581,0.000015186692,0.000009310658,0.00007908333],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0001523995,0.0016879251,0.00051125034,0.001122142,0.0006001619,0.00032610047,0.0003867504,0.0008732084,0.0029907906],"category_scores_gemma":[0.0004947084,0.00044230028,0.00032248232,0.0005602826,0.0015262266,0.00036278818,0.0008933056,0.00068734266,0.0005517677],"study_design_candidate":"bench_or_experimental","study_design_consensus":"bench_or_experimental","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0025342926,0.00020027897,0.01904207,0.0004644407,0.00033880645,0.17119439,0.00053625146,0.001484332,0.75671095,0.009598235,0.0028032367,0.035092708],"study_design_scores_gemma":[0.0009394663,0.0010395533,0.2030775,0.000112678725,0.0006322928,0.384602,0.0006295752,0.004593514,0.35774872,0.009830253,0.03653307,0.0002614151],"about_ca_topic_score_codex":0.0015484648,"about_ca_topic_score_gemma":0.0018548666,"teacher_disagreement_score":0.0029907906,"about_ca_system_score_codex":0.00043545224,"about_ca_system_score_gemma":0.0006250821,"threshold_uncertainty_score":0.010005176},"labels":[],"label_agreement":null},{"id":"W1551014578","doi":"10.1038/79208","title":"Mutations in ATP6N1B, encoding a new kidney vacuolar proton pump 116-kD subunit, cause recessive distal renal tubular acidosis with preserved hearing","year":2000,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Ion Transport and Channel Regulation","field":"Biochemistry, Genetics and Molecular Biology","cited_by":420,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Hospital for Sick Children","funders":"","keywords":"Biology; Distal renal tubular acidosis; Nephron; Kidney; Intercalated Cell; Protein subunit; Renal tubular acidosis; Molecular biology; Metabolic acidosis; Internal medicine; Endocrinology; Gene; Acidosis; Genetics; Medicine","score_opus":0.010532652849865792,"score_gpt":0.24782866146435248,"score_spread":0.2372960086144867,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1551014578","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9814652,0.0017596146,0.008706612,0.001122072,0.00052859413,0.00010701358,0.0020254238,0.00046299092,0.0038223264],"genre_scores_gemma":[0.99334246,0.00047521904,0.002721868,0.000176946,0.00011365766,0.000026015094,0.0005900051,0.00013269768,0.0024211416],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9994677,0.00007909968,0.00005812067,0.00010276822,0.00022822816,0.00006402084],"domain_scores_gemma":[0.99895763,0.00033078354,0.00027104825,0.00003412572,0.000053680124,0.00035274224],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00033404157,0.003077723,0.00084330305,0.0012516887,0.000782019,0.00046687725,0.0009529542,0.0023869176,0.0026910396],"category_scores_gemma":[0.0014280077,0.00047883554,0.00059565087,0.0008136162,0.0013089654,0.0003162626,0.0007301526,0.0010129103,0.00087565545],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0027158626,0.00037631654,0.019988071,0.00048329958,0.00039445763,0.352114,0.0010309594,0.0024114414,0.5936294,0.0025661741,0.0043496694,0.019940363],"study_design_scores_gemma":[0.0012297621,0.001204825,0.15319851,0.00031880525,0.0008127704,0.70337313,0.0007402999,0.011258799,0.10997428,0.00360218,0.013971038,0.00031555202],"about_ca_topic_score_codex":0.0026372608,"about_ca_topic_score_gemma":0.0026049067,"teacher_disagreement_score":0.003077723,"about_ca_system_score_codex":0.0004938189,"about_ca_system_score_gemma":0.00032728555,"threshold_uncertainty_score":0.0090023875},"labels":[],"label_agreement":null},{"id":"W1551996591","doi":"10.1038/90058","title":"Human mitochondrial DNA deletions associated with mutations in the gene encoding Twinkle, a phage T7 gene 4-like protein localized in mitochondria","year":2001,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Mitochondrial Function and Pathology","field":"Biochemistry, Genetics and Molecular Biology","cited_by":882,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Montreal Neurological Institute and Hospital; McGill University","funders":"","keywords":"Biology; Mitochondrial DNA; Genetics; Gene; Human mitochondrial genetics; Helicase; Mutation; Molecular biology; RNA","score_opus":0.01178110231607172,"score_gpt":0.26312083841164297,"score_spread":0.25133973609557125,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1551996591","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9954899,0.00044985343,0.0021420065,0.00010553888,0.000049639642,0.000046590343,0.00053109316,0.00008304494,0.0011024375],"genre_scores_gemma":[0.9973911,0.00020910487,0.00084202463,0.000060153892,0.00002339657,0.000014703002,0.000555903,0.000036768182,0.0008667259],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9997309,0.000051568433,0.000042334086,0.000071123795,0.000065615975,0.000038423776],"domain_scores_gemma":[0.999143,0.00021306814,0.0003593898,0.000077066084,0.00006678654,0.00014071385],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00015329408,0.0010963342,0.00055182894,0.00061528647,0.00047912978,0.00030514755,0.00029718623,0.0010682127,0.0021391292],"category_scores_gemma":[0.0007698591,0.000361829,0.00049652765,0.000754447,0.00088659476,0.00022281519,0.00051887415,0.0006279076,0.0007471321],"study_design_candidate":"bench_or_experimental","study_design_consensus":"bench_or_experimental","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0039800396,0.00023520864,0.01141701,0.00039621227,0.00045571043,0.046080768,0.0006138658,0.001701277,0.92316496,0.0011236662,0.00097089837,0.009860351],"study_design_scores_gemma":[0.0011295286,0.002728187,0.19497184,0.00018396198,0.0012813036,0.2592731,0.0006917433,0.004170006,0.5177259,0.0024985685,0.015131857,0.00021398114],"about_ca_topic_score_codex":0.0011567363,"about_ca_topic_score_gemma":0.0014588255,"teacher_disagreement_score":0.0021391292,"about_ca_system_score_codex":0.0002509407,"about_ca_system_score_gemma":0.00027792866,"threshold_uncertainty_score":0.007156074},"labels":[],"label_agreement":null},{"id":"W1552907768","doi":"10.1038/79116","title":"Mutations in MKKS cause Bardet-Biedl syndrome","year":2000,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Genetic and Kidney Cyst Diseases","field":"Biochemistry, Genetics and Molecular Biology","cited_by":270,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Toronto; Memorial University of Newfoundland","funders":"National Eye Institute","keywords":"Polydactyly; Proband; Genetics; Biology; Missense mutation; Compound heterozygosity; Retinitis pigmentosa; Bardet–Biedl syndrome; X-linked recessive inheritance; Frameshift mutation; Allele; Exon; X chromosome; Mutation; Phenotype; Gene","score_opus":0.0048080289317787295,"score_gpt":0.24768105848469057,"score_spread":0.24287302955291185,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1552907768","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9794606,0.003751282,0.004698904,0.0015361932,0.00032131476,0.00004177425,0.0010593417,0.00053910207,0.008591354],"genre_scores_gemma":[0.9959265,0.000500174,0.0017577886,0.00016213866,0.000075704615,0.000013907016,0.00018551497,0.000042177333,0.0013361524],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9997117,0.000025067238,0.00003869855,0.00006083818,0.00011540996,0.000048273094],"domain_scores_gemma":[0.9993486,0.00015947747,0.0002373691,0.000025613354,0.000037231013,0.00019172352],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0001773955,0.0013281913,0.0005558104,0.0017799634,0.00053122983,0.000585461,0.00067380344,0.0025015266,0.0035845204],"category_scores_gemma":[0.0008852109,0.0005085931,0.0003565409,0.0009805635,0.0010055648,0.0005892386,0.0009196054,0.0009861303,0.0017114354],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0018077185,0.00019255151,0.034908015,0.0004596122,0.0002966502,0.36956432,0.0007221367,0.0013167032,0.55744725,0.0059899194,0.0045078574,0.022787288],"study_design_scores_gemma":[0.0005002725,0.00035311197,0.12395846,0.00015192098,0.0005622183,0.64077467,0.00042086086,0.0052131107,0.19451477,0.0058709052,0.027465032,0.00021465664],"about_ca_topic_score_codex":0.0012276612,"about_ca_topic_score_gemma":0.0010817942,"teacher_disagreement_score":0.0035845204,"about_ca_system_score_codex":0.00055880874,"about_ca_system_score_gemma":0.000345376,"threshold_uncertainty_score":0.011991441},"labels":[],"label_agreement":null},{"id":"W1573866353","doi":"10.1038/90081","title":"Ltap, a mammalian homolog of Drosophila Strabismus/Van Gogh, is altered in the mouse neural tube mutant Loop-tail","year":2001,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Developmental Biology and Gene Regulation","field":"Biochemistry, Genetics and Molecular Biology","cited_by":499,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Alberta; McGill University","funders":"National Cancer Institute","keywords":"Neural tube; Biology; Dishevelled; Frizzled; Convergent extension; Neuroectoderm; Genetics; Genetic screen; Neural plate; Mutant; Axon guidance; Gene; Cell biology; Embryo; Embryogenesis; Wnt signaling pathway; Embryonic stem cell; Mesoderm","score_opus":0.008209169283375431,"score_gpt":0.24913436778273182,"score_spread":0.2409251984993564,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1573866353","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99103266,0.0010186122,0.004609665,0.00014819301,0.00007452579,0.000023578494,0.0010187434,0.00040327353,0.0016706242],"genre_scores_gemma":[0.9918829,0.00036221268,0.0015130256,0.00007330758,0.000015500702,0.000036612444,0.0009880388,0.00021578229,0.004912607],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9996561,0.000034934015,0.000038543436,0.00007566017,0.0001350525,0.000059862974],"domain_scores_gemma":[0.99917275,0.00009004563,0.00039135045,0.00005333333,0.000046422472,0.00024595528],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0001469229,0.00096574804,0.00040218915,0.0012932257,0.0005604516,0.0006927176,0.0010425508,0.0011099619,0.0030725817],"category_scores_gemma":[0.00033736794,0.00053743384,0.00040290694,0.0004665002,0.0009947025,0.00040266677,0.0007799214,0.0010037028,0.0017737917],"study_design_candidate":"bench_or_experimental","study_design_consensus":"bench_or_experimental","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00012089045,0.000010243839,0.00021121968,0.000022656921,0.00000764175,0.00048566304,0.000017655158,0.00007489298,0.99835664,0.00018264168,0.00003511459,0.00047476793],"study_design_scores_gemma":[0.000057616686,0.0001108078,0.020102412,0.000017063992,0.000072302464,0.0041872724,0.00011184881,0.0014606168,0.97001135,0.0002896863,0.003553775,0.000025191159],"about_ca_topic_score_codex":0.0013851402,"about_ca_topic_score_gemma":0.0020016436,"teacher_disagreement_score":0.0030725817,"about_ca_system_score_codex":0.0005264804,"about_ca_system_score_gemma":0.00035403026,"threshold_uncertainty_score":0.010278821},"labels":[],"label_agreement":null},{"id":"W1576226022","doi":"10.1038/ng727","title":"Pharmacologic rescue of lethal seizures in mice deficient in succinate semialdehyde dehydrogenase","year":2001,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Diet and metabolism studies","field":"Medicine","cited_by":158,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Hospital for Sick Children","funders":"National Institute of Neurological Disorders and Stroke; National Institute on Aging","keywords":"Vigabatrin; Ataxia; Endocrinology; Pharmacology; Taurine; Bicuculline; Biology; Internal medicine; Phenobarbital; Epilepsy; Anticonvulsant; Medicine; GABAA receptor; Receptor; Biochemistry; Amino acid; Neuroscience","score_opus":0.014841437606430743,"score_gpt":0.3142002301430439,"score_spread":0.2993587925366131,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1576226022","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9845931,0.0016393561,0.0060313884,0.0013393349,0.00026723254,0.00012567797,0.0019544745,0.000500708,0.0035486084],"genre_scores_gemma":[0.9846608,0.0021077197,0.0036939408,0.0002176619,0.00006429411,0.00013940834,0.0011764212,0.00018914598,0.007750523],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9997421,0.00003760555,0.00004437064,0.000042389343,0.000060316044,0.00007325423],"domain_scores_gemma":[0.9995403,0.00007325201,0.00014732598,0.000058132653,0.00003787449,0.00014320441],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0002578645,0.0010012315,0.00064575445,0.0008687654,0.00036565488,0.00043771832,0.0007796695,0.00084110454,0.0029311867],"category_scores_gemma":[0.0002767694,0.00038030942,0.00052308146,0.00035410706,0.00086316885,0.00046380833,0.00039313667,0.0017397426,0.00072963577],"study_design_candidate":"bench_or_experimental","study_design_consensus":"bench_or_experimental","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0004958628,0.0001225353,0.000094150644,0.00004370569,0.000019355148,0.00020307914,0.000024614877,0.00012280521,0.9966395,0.0005749247,0.00017191176,0.0014875069],"study_design_scores_gemma":[0.00022186089,0.00076234684,0.0011156431,0.000017284432,0.00004870356,0.00046919126,0.00008711079,0.0005360717,0.9944857,0.00020647822,0.0020395606,0.0000101649],"about_ca_topic_score_codex":0.0011750584,"about_ca_topic_score_gemma":0.0019196458,"teacher_disagreement_score":0.0029311867,"about_ca_system_score_codex":0.00038362242,"about_ca_system_score_gemma":0.00054779404,"threshold_uncertainty_score":0.009805739},"labels":[],"label_agreement":null},{"id":"W1589042524","doi":"10.1038/85817","title":"SPTLC1 is mutated in hereditary sensory neuropathy, type 1","year":2001,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":293,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Toronto Western Hospital","funders":"","keywords":"Biology; Genetics; Locus (genetics); Sensory neuropathy; Gene; Sensory system; Dorsum; Anatomy; Neuroscience; Internal medicine; Medicine","score_opus":0.02978553828112258,"score_gpt":0.2801146467568478,"score_spread":0.2503291084757252,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1589042524","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99208415,0.0010272423,0.0012614088,0.00046344663,0.00013075193,0.00003315866,0.0008667518,0.00017127277,0.0039617773],"genre_scores_gemma":[0.9975387,0.00018111974,0.0006862795,0.00009153456,0.000050300983,0.000010555512,0.00033784498,0.00003768735,0.0010659256],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.99977404,0.00001913817,0.000026266644,0.000060705137,0.00007968072,0.000040189207],"domain_scores_gemma":[0.99942636,0.00019309009,0.00016021615,0.000021454782,0.00006600702,0.00013282968],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0001765664,0.0010828824,0.00055378483,0.0014048062,0.0008880156,0.00046025414,0.00089602784,0.002054641,0.004556308],"category_scores_gemma":[0.0010703513,0.00021668285,0.00039113933,0.0008789314,0.00076402625,0.00030831926,0.000536994,0.00077743485,0.00075885985],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0030254624,0.00029812066,0.053173535,0.00059195835,0.00029332805,0.39294544,0.0010189336,0.0023529227,0.50293297,0.0024325927,0.0073720207,0.033562705],"study_design_scores_gemma":[0.0005512145,0.00072567986,0.23643391,0.00031652246,0.0007492247,0.5304211,0.00090759736,0.010609583,0.20298272,0.0035152212,0.012595354,0.00019190725],"about_ca_topic_score_codex":0.0041070515,"about_ca_topic_score_gemma":0.0030596256,"teacher_disagreement_score":0.004556308,"about_ca_system_score_codex":0.00061733864,"about_ca_system_score_gemma":0.00038273024,"threshold_uncertainty_score":0.015242338},"labels":[],"label_agreement":null},{"id":"W1589206938","doi":"10.1038/ng1001-194","title":"A radiation hybrid transcript map of the mouse genome","year":2001,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Genetic Mapping and Diversity in Plants and Animals","field":"Biochemistry, Genetics and Molecular Biology","cited_by":36,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Centre hospitalier de l'Université Laval","funders":"","keywords":"Biology; Expressed sequence tag; Radiation hybrid mapping; Genetics; Sequence-tagged site; Homology (biology); Genome; Gene mapping; Gene; Computational biology; Zebrafish; Human genome; In situ hybridization; Chromosome; Gene expression","score_opus":0.006482464352859129,"score_gpt":0.20854802496758956,"score_spread":0.20206556061473044,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1589206938","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.92060035,0.005023331,0.05022525,0.0006043068,0.00012166163,0.00010459181,0.00396292,0.0009709544,0.018386684],"genre_scores_gemma":[0.9241394,0.0025002484,0.028875574,0.00032886257,0.00007072854,0.00011314661,0.010071793,0.00024715875,0.03365322],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9999074,0.0000066503917,0.0000037682191,0.00004552674,0.000018135244,0.000018553237],"domain_scores_gemma":[0.99985707,0.000040307586,0.00002924307,0.000015627049,0.000015029087,0.000042725984],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0001644755,0.00039181215,0.00022667392,0.0012106512,0.0004885617,0.00033109362,0.00042035175,0.00042001248,0.0044292086],"category_scores_gemma":[0.0000988956,0.0004047534,0.00061183603,0.0004328982,0.00031327936,0.00025857924,0.00031842064,0.00075995293,0.0016243482],"study_design_candidate":"bench_or_experimental","study_design_consensus":"bench_or_experimental","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00014552915,0.0000115461635,0.0002462713,0.000034953784,0.000011598253,0.00019928275,0.000037416954,0.00007565132,0.99333185,0.0016111159,0.00013039938,0.0041644],"study_design_scores_gemma":[0.00020942942,0.00064424885,0.0777171,0.00011558955,0.00028183128,0.0030315947,0.0001523107,0.0015522082,0.8649287,0.0054401155,0.045878377,0.000048504215],"about_ca_topic_score_codex":0.0014165248,"about_ca_topic_score_gemma":0.003155044,"teacher_disagreement_score":0.0044292086,"about_ca_system_score_codex":0.00030543073,"about_ca_system_score_gemma":0.00023782613,"threshold_uncertainty_score":0.014817238},"labels":[],"label_agreement":null},{"id":"W1594539479","doi":"10.1038/82565","title":"Disruption of the uncoupling protein-2 gene in mice reveals a role in immunity and reactive oxygen species production","year":2000,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Adipose Tissue and Metabolism","field":"Medicine","cited_by":1075,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Université Laval","funders":"National Institute of Diabetes and Digestive and Kidney Diseases","keywords":"Biology; Reactive oxygen species; Immunity; Inflammation; Wild type; Gene; Mitochondrial ROS; Spleen; Macrophage; Molecular biology; Immunology; Cell biology; In vitro; Immune system; Genetics; Mutant","score_opus":0.009628995607022336,"score_gpt":0.2588419043941911,"score_spread":0.24921290878716873,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1594539479","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.98217934,0.0015757817,0.011683204,0.0007802869,0.00010832611,0.000035414127,0.001099257,0.0004331045,0.0021052933],"genre_scores_gemma":[0.97687733,0.0018691802,0.012029886,0.00032338392,0.000059975388,0.00007398418,0.001081668,0.00032837858,0.0073562018],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9997583,0.000035046047,0.000021250624,0.00007784787,0.000064603235,0.000042960735],"domain_scores_gemma":[0.99953794,0.00007009593,0.00021858868,0.000038653907,0.000018326362,0.00011637602],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00018589721,0.0010730344,0.00041191935,0.0012336517,0.00034939128,0.00055817363,0.0005875458,0.0010198774,0.001507343],"category_scores_gemma":[0.00021197488,0.0006592881,0.00040512343,0.0004015191,0.0010622714,0.0003980472,0.00045893347,0.001586789,0.00047206698],"study_design_candidate":"bench_or_experimental","study_design_consensus":"bench_or_experimental","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00034355154,0.00003064728,0.0002002456,0.000014204327,0.000008913067,0.00015152278,0.000012384107,0.000115478004,0.9977182,0.00052867085,0.00006147894,0.0008146081],"study_design_scores_gemma":[0.00016968866,0.00023660823,0.009587524,0.000024042974,0.00009283472,0.0013993497,0.00007190616,0.0019363655,0.9814331,0.0008759592,0.0041439934,0.000028704328],"about_ca_topic_score_codex":0.00079594075,"about_ca_topic_score_gemma":0.0017672578,"teacher_disagreement_score":0.001507343,"about_ca_system_score_codex":0.00052820594,"about_ca_system_score_gemma":0.00032360828,"threshold_uncertainty_score":0.005042553},"labels":[],"label_agreement":null},{"id":"W1598899303","doi":"10.1038/ng1001-223","title":"Genetic variation in the 5q31 cytokine gene cluster confers susceptibility to Crohn disease","year":2001,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Inflammatory Bowel Disease","field":"Biochemistry, Genetics and Molecular Biology","cited_by":782,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Cégep de Chicoutimi; Centre Hospitalier Universitaire de Sherbrooke; McGill Genome Centre; McGill University; University of Toronto; SickKids Foundation; Mount Sinai Hospital; Hospital for Sick Children","funders":"Hospital for Sick Children; University of Toronto","keywords":"Biology; Genetics; Linkage disequilibrium; Locus (genetics); Haplotype; Single-nucleotide polymorphism; Chromosomal region; Gene mapping; Gene; Genetic association; Microsatellite; Allele; Genotype; Chromosome","score_opus":0.005984424926402407,"score_gpt":0.24744649343993988,"score_spread":0.24146206851353746,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1598899303","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9981363,0.00025423066,0.000691035,0.00012477297,0.00001986139,0.0000100692005,0.00015910456,0.000019860749,0.00058468175],"genre_scores_gemma":[0.9990889,0.000055083434,0.00046659136,0.000033669774,0.00001921676,0.000004701753,0.00012722846,0.000007035338,0.0001976442],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9994369,0.00021665671,0.000049775183,0.00010458216,0.000108168395,0.000083822815],"domain_scores_gemma":[0.9992354,0.0003362433,0.0001923576,0.000052567884,0.0000519959,0.0001313946],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00033412437,0.0005719578,0.00036494457,0.0011288244,0.00046824903,0.0002684698,0.00031280066,0.0008431102,0.0031705406],"category_scores_gemma":[0.0010318329,0.00023641696,0.00043126752,0.00058774825,0.00035267053,0.00014705717,0.00030752926,0.00049459736,0.0003083995],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.005111348,0.0002572018,0.22208546,0.00011915323,0.0003865188,0.01427154,0.00054512516,0.0018877481,0.7430921,0.0017103509,0.00065609574,0.00987734],"study_design_scores_gemma":[0.00025067368,0.000630914,0.9539769,0.00006455686,0.00032175722,0.013400524,0.00023531797,0.0032950041,0.024580302,0.0014803632,0.0017146511,0.000049029117],"about_ca_topic_score_codex":0.002187295,"about_ca_topic_score_gemma":0.0016971366,"teacher_disagreement_score":0.0031705406,"about_ca_system_score_codex":0.00027385115,"about_ca_system_score_gemma":0.0002257508,"threshold_uncertainty_score":0.010606527},"labels":[],"label_agreement":null},{"id":"W1599843882","doi":"10.1038/81619","title":"Mutations in NYX, encoding the leucine-rich proteoglycan nyctalopin, cause X-linked complete congenital stationary night blindness","year":2000,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Retinal Development and Disorders","field":"Biochemistry, Genetics and Molecular Biology","cited_by":352,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"McGill University; Montreal Children's Hospital; University of Victoria; University of Calgary","funders":"National Eye Institute","keywords":"Biology; Proteoglycan; Leucine; Genetics; Blindness; Mutation; Gene; Amino acid; Medicine","score_opus":0.013312878510957646,"score_gpt":0.2666775845821614,"score_spread":0.25336470607120376,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1599843882","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9881216,0.0015317897,0.005059628,0.00023387841,0.00007642808,0.00004466837,0.00087376765,0.00028633612,0.0037718662],"genre_scores_gemma":[0.9945516,0.0006537894,0.0013979252,0.000049890332,0.000022363507,0.000016006838,0.00042229792,0.00004138283,0.0028447742],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99987173,0.000018478238,0.000010914135,0.000025202236,0.000056579225,0.000016955388],"domain_scores_gemma":[0.99974245,0.000070591654,0.00008842008,0.000012606525,0.000014749968,0.00007116003],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00008355099,0.0013555476,0.00029563787,0.00059767964,0.00031011723,0.0002617632,0.00023522977,0.00064832537,0.00173508],"category_scores_gemma":[0.00030506172,0.00023798694,0.00020421717,0.0002162053,0.00089952786,0.00023071759,0.00067281246,0.0004924597,0.0005302229],"study_design_candidate":"bench_or_experimental","study_design_consensus":"bench_or_experimental","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00059481186,0.000078564415,0.0077399886,0.0001564778,0.00009412044,0.025159303,0.0001964825,0.00073183386,0.94699395,0.0018852727,0.0012164436,0.015152733],"study_design_scores_gemma":[0.0003645666,0.00068760174,0.19292513,0.000096571326,0.00030190963,0.14353251,0.00052515016,0.0076702177,0.63302726,0.0022038165,0.018556856,0.000108428125],"about_ca_topic_score_codex":0.0012335542,"about_ca_topic_score_gemma":0.0017829075,"teacher_disagreement_score":0.00173508,"about_ca_system_score_codex":0.00024618427,"about_ca_system_score_gemma":0.00022175233,"threshold_uncertainty_score":0.005804479},"labels":[],"label_agreement":null},{"id":"W1604195255","doi":"10.1038/79102","title":"Pidd, a new death-domain–containing protein, is induced by p53 and promotes apoptosis","year":2000,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Cancer-related Molecular Pathways","field":"Medicine","cited_by":353,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Princess Margaret Cancer Centre; University of Toronto; Ontario Institute for Cancer Research","funders":"","keywords":"Biology; Apoptosis; P53 protein; Cell biology; Death domain; Domain (mathematical analysis); Genetics; Programmed cell death; Protein stability; Cancer research; Computational biology","score_opus":0.010828867876433534,"score_gpt":0.25457742838469694,"score_spread":0.2437485605082634,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1604195255","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.97197735,0.008447479,0.013311365,0.00049638696,0.00025529522,0.000043642558,0.0006907683,0.00041723307,0.004360447],"genre_scores_gemma":[0.9892252,0.0021973187,0.003972579,0.000108858345,0.000036498393,0.00002468051,0.0011772359,0.00002334748,0.0032342495],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99990237,0.000010679586,0.000008880352,0.000021517078,0.0000375052,0.000018925119],"domain_scores_gemma":[0.9998424,0.00002299775,0.00005282594,0.000017007716,0.000012137701,0.000052589192],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00017375013,0.00028755944,0.00030149752,0.00046200864,0.00029596078,0.0004935509,0.00026196567,0.00027008695,0.0008563563],"category_scores_gemma":[0.00019200805,0.00016228038,0.00022934309,0.00022203581,0.00033577144,0.00026667942,0.00032131275,0.0005265295,0.0003709341],"study_design_candidate":"bench_or_experimental","study_design_consensus":"bench_or_experimental","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0004612799,0.00004717516,0.0016086982,0.00007964298,0.000017708358,0.0009847063,0.000014028224,0.00016826157,0.98879015,0.00052961457,0.0004530295,0.00684573],"study_design_scores_gemma":[0.00011679758,0.00037481735,0.019501485,0.000011703479,0.0000527282,0.006260032,0.0000421834,0.0023790002,0.95338696,0.00044566387,0.017415266,0.0000132908235],"about_ca_topic_score_codex":0.00010768102,"about_ca_topic_score_gemma":0.000179889,"teacher_disagreement_score":0.0008563563,"about_ca_system_score_codex":0.0006246227,"about_ca_system_score_gemma":0.00016031574,"threshold_uncertainty_score":0.0045319796},"labels":[],"label_agreement":null},{"id":"W1608345078","doi":"10.1038/ng574","title":"Imprinted X inactivation maintained by a mouse Polycomb group gene","year":2001,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Epigenetics and DNA Methylation","field":"Biochemistry, Genetics and Molecular Biology","cited_by":338,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Mount Sinai Hospital; Lunenfeld-Tanenbaum Research Institute; University of Calgary","funders":"","keywords":"Biology; X-inactivation; Embryonic stem cell; Dosage compensation; XIST; Genomic imprinting; Genetics; Transgene; Embryo; Gene; Molecular biology; Gene silencing; X chromosome; Chromosome; Cell biology; Embryogenesis; DNA methylation; Gene expression","score_opus":0.004697688994039703,"score_gpt":0.24647597776293517,"score_spread":0.24177828876889546,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1608345078","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9893658,0.0013931809,0.004069044,0.00016781146,0.000084556435,0.000023089848,0.000297044,0.00028512388,0.004314307],"genre_scores_gemma":[0.99021834,0.00039150668,0.0012240057,0.00004339661,0.000022850705,0.000022304217,0.00030688185,0.00008003613,0.007690616],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9996363,0.00003784758,0.000025433523,0.00009385689,0.00011585414,0.00009077917],"domain_scores_gemma":[0.9995053,0.0000757029,0.00016292192,0.0001116778,0.000026968384,0.000117490024],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00025031535,0.000493753,0.00031061316,0.00076719734,0.00037189136,0.0005887059,0.0009006697,0.00052892836,0.0024955678],"category_scores_gemma":[0.00027353564,0.00047917865,0.00032503367,0.00037850492,0.0007650684,0.00036971192,0.0005957536,0.0008511883,0.0008041453],"study_design_candidate":"bench_or_experimental","study_design_consensus":"bench_or_experimental","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00017444568,0.000015597047,0.0002871135,0.000015139655,0.000007891259,0.00018796533,0.000020032869,0.00003721509,0.9976502,0.0007359967,0.000040734325,0.00082772283],"study_design_scores_gemma":[0.000055164088,0.0001546779,0.0071052383,0.0000053988556,0.00003761513,0.0007808912,0.00003109082,0.0003809998,0.9891874,0.00024906802,0.0020063887,0.0000060032403],"about_ca_topic_score_codex":0.00074080593,"about_ca_topic_score_gemma":0.0014215735,"teacher_disagreement_score":0.0024955678,"about_ca_system_score_codex":0.00045378637,"about_ca_system_score_gemma":0.000223731,"threshold_uncertainty_score":0.008348465},"labels":[],"label_agreement":null},{"id":"W1686085663","doi":"10.1038/ng753","title":"A 1.5 million–base pair inversion polymorphism in families with Williams-Beuren syndrome","year":2001,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Williams Syndrome Research","field":"Neuroscience","cited_by":350,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Hospital for Sick Children; University Health Network; Canada Research Chairs; University of Toronto","funders":"Canadian Institutes of Health Research; University of Arizona; Yale University","keywords":"Biology; Genetics; Chromosomal inversion; Haploinsufficiency; Proband; Fluorescence in situ hybridization; Chromosome; Phenotype; Gene; Karyotype","score_opus":0.021269867961441966,"score_gpt":0.2679939696801198,"score_spread":0.2467241017186778,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1686085663","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9961403,0.00039874951,0.0009268578,0.00044463956,0.0001221302,0.000030136312,0.00028078578,0.000048421432,0.0016080306],"genre_scores_gemma":[0.9984296,0.00008729559,0.00053120404,0.00014424889,0.000087256805,0.000012351004,0.00011761725,0.000022115399,0.00056829123],"study_design_codex":"case_report","study_design_gemma":"observational","domain_scores_codex":[0.9994906,0.00010310249,0.0000703515,0.00013877808,0.00010552012,0.00009158851],"domain_scores_gemma":[0.99849045,0.00065914536,0.00034192714,0.000050255912,0.00010550172,0.00035273837],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0002526158,0.0016761252,0.00077458046,0.002261908,0.0013669468,0.0005265167,0.0011926424,0.0023252545,0.005681019],"category_scores_gemma":[0.0024696095,0.0003707457,0.00081450865,0.0011711306,0.00082065084,0.00039465388,0.0005837927,0.0012931993,0.0007818007],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.005747555,0.0014061308,0.16138692,0.00023749105,0.0007240336,0.4923603,0.004049562,0.0013691668,0.30266255,0.0030720043,0.0025908002,0.024393633],"study_design_scores_gemma":[0.0005291306,0.0017352751,0.44745398,0.00019883334,0.0012063539,0.5070635,0.001768316,0.003725362,0.029548358,0.0020065345,0.0045329197,0.00023142097],"about_ca_topic_score_codex":0.0041357353,"about_ca_topic_score_gemma":0.002415835,"teacher_disagreement_score":0.005681019,"about_ca_system_score_codex":0.00036728638,"about_ca_system_score_gemma":0.00036498252,"threshold_uncertainty_score":0.019004881},"labels":[],"label_agreement":null},{"id":"W1699214082","doi":"10.1038/ng.3293","title":"A Sleeping Beauty forward genetic screen identifies new genes and pathways driving osteosarcoma development and metastasis","year":2015,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Sarcoma Diagnosis and Treatment","field":"Medicine","cited_by":244,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Ontario Institute for Cancer Research","funders":"National Center for Advancing Translational Sciences; National Institute of Arthritis and Musculoskeletal and Skin Diseases; National Cancer Institute","keywords":"Osteosarcoma; Biology; Metastasis; Cancer research; Gene; ErbB; PI3K/AKT/mTOR pathway; Genetic screen; Genome instability; Signal transduction; Cancer; Genetics; Phenotype; DNA damage; DNA","score_opus":0.03405641952822479,"score_gpt":0.2774755764577278,"score_spread":0.243419156929503,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1699214082","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.96318287,0.0016104392,0.021837655,0.0011753717,0.00022702558,0.00019827505,0.004445706,0.0008438145,0.0064788917],"genre_scores_gemma":[0.9666894,0.0019019272,0.014635357,0.00055788347,0.000044253276,0.00008215992,0.003916091,0.00023200242,0.011940919],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9997142,0.000025701704,0.000017459024,0.00006203625,0.00013586556,0.000044823068],"domain_scores_gemma":[0.9996964,0.00013229167,0.00006238369,0.000028632025,0.00002409486,0.00005632721],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00038342518,0.0007734571,0.000495272,0.00089219725,0.00040918816,0.00048676739,0.0005139582,0.00062413857,0.0056237313],"category_scores_gemma":[0.00029242842,0.0005069519,0.0009997388,0.0004798755,0.0006375727,0.00020226785,0.00040482596,0.0009453389,0.00076909136],"study_design_candidate":"bench_or_experimental","study_design_consensus":"bench_or_experimental","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00017674609,0.00005708114,0.00088884664,0.000049625694,0.000035350804,0.000761682,0.000026635116,0.00026543462,0.9930883,0.00061826705,0.0003787731,0.0036531738],"study_design_scores_gemma":[0.00024403074,0.0010710226,0.016118938,0.000023564226,0.0004043026,0.0050455746,0.00013695544,0.0045428365,0.95589626,0.0007212335,0.015753224,0.00004197698],"about_ca_topic_score_codex":0.0014688371,"about_ca_topic_score_gemma":0.0047453414,"teacher_disagreement_score":0.0056237313,"about_ca_system_score_codex":0.0002966945,"about_ca_system_score_gemma":0.0005617633,"threshold_uncertainty_score":0.018813252},"labels":[],"label_agreement":null},{"id":"W1764005853","doi":"10.1038/ng.3304","title":"Factors influencing success of clinical genome sequencing across a broad spectrum of disorders","year":2015,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Genomics and Rare Diseases","field":"Biochemistry, Genetics and Molecular Biology","cited_by":388,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Hospital for Sick Children","funders":"Biotechnology and Biological Sciences Research Council; Medical Research Council; Schweizerischer Nationalfonds zur Förderung der Wissenschaftlichen Forschung; National Institute for Health and Care Research; Cancer Research UK; Action Medical Research; Academy of Medical Sciences; British Heart Foundation; Wellcome Trust","keywords":"Biology; Broad spectrum; Genetics; Computational biology; Genome; DNA sequencing; Evolutionary biology; Gene","score_opus":0.027897789978631113,"score_gpt":0.33991380154357625,"score_spread":0.31201601156494513,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1764005853","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.98029137,0.002526298,0.0023288787,0.005345324,0.00010143938,0.000048612234,0.00036906207,0.000059216713,0.008929877],"genre_scores_gemma":[0.99774855,0.00033241216,0.00094562303,0.00048735546,0.00006891476,0.000015569382,0.00013441173,0.000056115154,0.00021108055],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.97641695,0.009869579,0.0037047297,0.0022831613,0.004363359,0.0033622251],"domain_scores_gemma":[0.7304545,0.20785068,0.022420797,0.009261717,0.015474308,0.014537956],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.033327483,0.00026511477,0.0005151169,0.0031548548,0.0010905998,0.0025887166,0.0015048118,0.0013799118,0.0058523794],"category_scores_gemma":[0.18571714,0.00027513664,0.00048926007,0.0026641719,0.0017610742,0.0023262415,0.0020948579,0.0016970356,0.0007656669],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0005219914,0.0000911286,0.96831405,0.00007866032,0.00019679837,0.0007517827,0.0014162267,0.00058296864,0.0015999808,0.0010243822,0.001449661,0.023972338],"study_design_scores_gemma":[0.000028020042,0.0003679814,0.97988164,0.0002879922,0.00018737043,0.0046846494,0.0031609174,0.0021873394,0.0015494546,0.0027355982,0.004893244,0.000035802994],"about_ca_topic_score_codex":0.004227609,"about_ca_topic_score_gemma":0.0074373716,"teacher_disagreement_score":0.033327483,"about_ca_system_score_codex":0.0009151294,"about_ca_system_score_gemma":0.0019699812,"threshold_uncertainty_score":0.17625463},"labels":[],"label_agreement":null},{"id":"W1775279835","doi":"10.1038/ng.3379","title":"Widespread non-additive and interaction effects within HLA loci modulate the risk of autoimmune diseases","year":2015,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Immune Cell Function and Interaction","field":"Immunology and Microbiology","cited_by":205,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Memorial University of Newfoundland; Toronto Western Hospital; University of Toronto","funders":"National Institute of Arthritis and Musculoskeletal and Skin Diseases; National Institute of General Medical Sciences; National Institutes of Health; Nederlandse Organisatie voor Wetenschappelijk Onderzoek; Alfried Krupp von Bohlen und Halbach-Stiftung; Deutsche Forschungsgemeinschaft; National Institute of Allergy and Infectious Diseases; European Commission; Instituto de Salud Carlos III; National Institute for Health and Care Research","keywords":"Rheumatoid arthritis; Autoimmune disease; Allele; Immunology; Psoriasis; Disease; Human leukocyte antigen; Type 1 diabetes; Autoimmunity; Biology; Dominance (genetics); Diabetes mellitus; Genetics; Medicine; Internal medicine; Antigen; Antibody; Gene; Endocrinology","score_opus":0.005562865132505694,"score_gpt":0.23521748150698366,"score_spread":0.22965461637447795,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1775279835","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99710864,0.0006357661,0.0013634805,0.000077465374,0.000014446727,0.0000034519385,0.00008487776,0.000025248288,0.0006865324],"genre_scores_gemma":[0.9989737,0.00013731747,0.0005222056,0.000028417195,0.000021596572,0.0000029422654,0.00003470635,0.00001097444,0.00026806167],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99868435,0.0006002583,0.00007901237,0.00027808454,0.00020003848,0.00015820801],"domain_scores_gemma":[0.99802005,0.00084747106,0.0005263269,0.00029259396,0.00010069146,0.00021293038],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00074491045,0.00042660703,0.00048575393,0.00079452747,0.00025677696,0.000802688,0.00040824138,0.0006559217,0.0026075419],"category_scores_gemma":[0.0017519973,0.00036051837,0.00043762446,0.0006404818,0.0004254719,0.00030763922,0.0005831259,0.00071511796,0.000311962],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.003375778,0.00034928822,0.51231587,0.00011940382,0.0016247905,0.0015704792,0.00034287848,0.001424242,0.44958842,0.0021134117,0.0004067234,0.026768679],"study_design_scores_gemma":[0.00005864127,0.0003919522,0.9830893,0.000013991041,0.00058127934,0.0015187422,0.00015882793,0.0024031792,0.009525132,0.00164512,0.00059023674,0.000023679708],"about_ca_topic_score_codex":0.0003903766,"about_ca_topic_score_gemma":0.000554324,"teacher_disagreement_score":0.0026075419,"about_ca_system_score_codex":0.00013862754,"about_ca_system_score_gemma":0.00015573952,"threshold_uncertainty_score":0.00872314},"labels":[],"label_agreement":null},{"id":"W1847545842","doi":"10.1038/74215","title":"Large-scale discovery and genotyping of single-nucleotide polymorphisms in the mouse","year":2000,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Genetic Mapping and Diversity in Plants and Animals","field":"Biochemistry, Genetics and Molecular Biology","cited_by":421,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"McGill Genome Centre; McGill University Health Centre","funders":"National Human Genome Research Institute","keywords":"Genotyping; Biology; Single-nucleotide polymorphism; SNP genotyping; Genetics; Molecular Inversion Probe; Microsatellite; Multiplex; Tag SNP; Genome; SNP array; Human genome; SNP; Computational biology; Genotype; Allele; Gene","score_opus":0.0071929199940417195,"score_gpt":0.21215744802983721,"score_spread":0.20496452803579548,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1847545842","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9553664,0.0018714913,0.03764839,0.00032544977,0.00006155873,0.00011639069,0.0024086214,0.00041653376,0.001785122],"genre_scores_gemma":[0.9487638,0.0016230673,0.041441392,0.00038201988,0.00003927383,0.0002617625,0.0022687612,0.00020188566,0.005017985],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.999428,0.000082706974,0.000046595316,0.00023612785,0.00014693958,0.000059688344],"domain_scores_gemma":[0.99934286,0.00019479083,0.00017292092,0.00012188827,0.00004920727,0.00011824806],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0009985808,0.0003752713,0.00041247378,0.0017403663,0.00033857135,0.0005323539,0.00069976324,0.0008645621,0.0009500155],"category_scores_gemma":[0.0007409334,0.00049340224,0.00053128577,0.0005695739,0.00049502676,0.00020060057,0.00048253065,0.0007443197,0.0002831487],"study_design_candidate":"bench_or_experimental","study_design_consensus":"bench_or_experimental","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00022282415,0.000049165283,0.002885212,0.000031190408,0.000049194405,0.00010964133,0.00005183112,0.0002728555,0.9864086,0.001161075,0.00013817771,0.008620363],"study_design_scores_gemma":[0.00041655928,0.00087131484,0.2430313,0.000114400194,0.00066542753,0.0028615014,0.00018786167,0.0059051155,0.7231609,0.003564434,0.019127462,0.0000937552],"about_ca_topic_score_codex":0.0015830639,"about_ca_topic_score_gemma":0.0035180368,"teacher_disagreement_score":0.0017403663,"about_ca_system_score_codex":0.00028616,"about_ca_system_score_gemma":0.00027581846,"threshold_uncertainty_score":0.0052810907},"labels":[],"label_agreement":null},{"id":"W1868727773","doi":"10.1038/ng.2747","title":"Genomic analysis identifies targets of convergent positive selection in drug-resistant Mycobacterium tuberculosis","year":2013,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Tuberculosis Research and Epidemiology","field":"Medicine","cited_by":12,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Provincial Health Services Authority; BC Centre for Disease Control; Université de Montréal","funders":"National Institute of Allergy and Infectious Diseases; Fogarty International Center; Schweizerischer Nationalfonds zur Förderung der Wissenschaftlichen Forschung","keywords":"Biology; Genetics; Mycobacterium tuberculosis; Gene; Genome; Drug resistance; Tuberculosis; Mutation; Negative selection","score_opus":0.0077059756996755565,"score_gpt":0.2826121213789817,"score_spread":0.2749061456793061,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1868727773","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99743867,0.00033197794,0.0011128468,0.000086074244,0.000009292552,0.000007813734,0.00015712273,0.000028656204,0.000827442],"genre_scores_gemma":[0.99909866,0.000059336377,0.00047986416,0.000065750326,0.000007760603,0.000003934075,0.000112375375,0.000009939717,0.00016236436],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9998338,0.000036069883,0.000007983202,0.000036285688,0.000053532447,0.00003232226],"domain_scores_gemma":[0.99954706,0.00019673434,0.00012462371,0.00003128873,0.0000329076,0.0000673553],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00014718287,0.00015895722,0.00029786018,0.0005772593,0.00022538175,0.00042196386,0.00023761374,0.00042873636,0.0014314197],"category_scores_gemma":[0.0006375849,0.00015530191,0.00025725208,0.00038726768,0.00028656353,0.0001298856,0.00031699854,0.00042023536,0.00024041653],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0005626303,0.00005471975,0.020347215,0.0000627939,0.0000491398,0.0006544878,0.00011097188,0.0006270109,0.9674749,0.00074941246,0.00016291055,0.00914389],"study_design_scores_gemma":[0.00014088604,0.0011435646,0.6944884,0.000040271632,0.00030622247,0.0039375247,0.00056595815,0.009181975,0.2836477,0.0029375413,0.0035673927,0.000042541327],"about_ca_topic_score_codex":0.0003465158,"about_ca_topic_score_gemma":0.00068582105,"teacher_disagreement_score":0.0014314197,"about_ca_system_score_codex":0.00017175307,"about_ca_system_score_gemma":0.000095718744,"threshold_uncertainty_score":0.004788518},"labels":[],"label_agreement":null},{"id":"W1880712737","doi":"10.1038/ng.3426","title":"Small island, big genetic discoveries","year":2015,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Genetic Associations and Epidemiology","field":"Biochemistry, Genetics and Molecular Biology","cited_by":23,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Université de Montréal; Montreal Heart Institute","funders":"","keywords":"Biology; Imputation (statistics); Genetics; Genetic variation; Phenotype; Genotype; Evolutionary biology; Genome-wide association study; Human genetic variation; Computational biology; Genome; Gene; Human genome; Single-nucleotide polymorphism","score_opus":0.02028909355062966,"score_gpt":0.26192491239275145,"score_spread":0.2416358188421218,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1880712737","genre_codex":"commentary","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":null,"domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.23947717,0.104534544,0.08902287,0.3453621,0.03173603,0.00048558594,0.012395126,0.0043499866,0.17263658],"genre_scores_gemma":[0.69651246,0.04758096,0.069395214,0.098175265,0.024666412,0.0004360729,0.0055299383,0.001305937,0.056397717],"study_design_codex":"design_other","study_design_gemma":"observational","domain_scores_codex":[0.9977816,0.00066709373,0.0001272559,0.00052665797,0.0006698433,0.00022753156],"domain_scores_gemma":[0.9789641,0.008460931,0.0010102419,0.0035939307,0.0030195345,0.0049511893],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.008626971,0.0006920914,0.001231478,0.002468503,0.0016861815,0.0044398457,0.0015443932,0.001904953,0.011420078],"category_scores_gemma":[0.015883964,0.0007629549,0.000670959,0.0022406208,0.003309999,0.0050507956,0.0043613613,0.0060582943,0.0021807472],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0010350782,0.0003130428,0.121940695,0.0017011414,0.0023062099,0.00378325,0.0028591638,0.00092333544,0.014183656,0.087615244,0.27951503,0.48382416],"study_design_scores_gemma":[0.00025979866,0.00027864234,0.23908454,0.00092510425,0.0011643558,0.0025142564,0.003783065,0.0014665577,0.0019983756,0.27079558,0.4775589,0.00017075555],"about_ca_topic_score_codex":0.0061126165,"about_ca_topic_score_gemma":0.014173578,"teacher_disagreement_score":0.011420078,"about_ca_system_score_codex":0.0016863549,"about_ca_system_score_gemma":0.003248873,"threshold_uncertainty_score":0.045624316},"labels":[],"label_agreement":null},{"id":"W1894493322","doi":"10.1038/88842","title":"Deletion of the hypoxia-response element in the vascular endothelial growth factor promoter causes motor neuron degeneration","year":2001,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Amyotrophic Lateral Sclerosis Research","field":"Medicine","cited_by":1010,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Toronto","funders":"Fonds Wetenschappelijk Onderzoek; Deutsche Forschungsgemeinschaft","keywords":"Vascular endothelial growth factor; Biology; Neurodegeneration; Angiogenesis; Hypoxia (environmental); Neuroprotection; Motor neuron; Vascular endothelial growth factor A; Neuropilin 1; Cancer research; Endocrinology; Internal medicine; Neuroscience; Spinal cord; Medicine; VEGF receptors; Chemistry","score_opus":0.021002925495795997,"score_gpt":0.28360946930087405,"score_spread":0.26260654380507803,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1894493322","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99448013,0.00022747726,0.0040619033,0.00014907926,0.000049469694,0.000011976428,0.00026295928,0.00012598168,0.0006309961],"genre_scores_gemma":[0.9957457,0.00021271234,0.0020657578,0.000052904426,0.000018940156,0.000018213877,0.00040548728,0.000085286534,0.0013949146],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9997986,0.000034044726,0.00003638136,0.00004509213,0.000048356265,0.00003751712],"domain_scores_gemma":[0.9994049,0.00019750826,0.00018633006,0.00005799676,0.000028164619,0.00012511839],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00020852331,0.00048638196,0.00037153612,0.00037922311,0.00022113242,0.00025537724,0.00043474077,0.0005930462,0.0013036261],"category_scores_gemma":[0.00041362792,0.0003124186,0.00040554383,0.00021153232,0.00060019107,0.00019548729,0.0003648465,0.0007593836,0.00057647517],"study_design_candidate":"bench_or_experimental","study_design_consensus":"bench_or_experimental","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00038375842,0.00007057923,0.00041123142,0.00004177926,0.000022502098,0.0010190721,0.000038746213,0.00038372623,0.99560034,0.00041487947,0.00010684348,0.0015064601],"study_design_scores_gemma":[0.00020087157,0.0003754794,0.013796376,0.000040552084,0.00013557628,0.00517859,0.00010754383,0.0052153724,0.97097373,0.0006656848,0.0032755067,0.000034746954],"about_ca_topic_score_codex":0.00086469925,"about_ca_topic_score_gemma":0.00095616677,"teacher_disagreement_score":0.0013036261,"about_ca_system_score_codex":0.0003962119,"about_ca_system_score_gemma":0.00028815086,"threshold_uncertainty_score":0.0043610334},"labels":[],"label_agreement":null},{"id":"W1904407543","doi":"10.1038/ng.3412","title":"Large-scale genomic analyses link reproductive aging to hypothalamic signaling, breast cancer susceptibility and BRCA1-mediated DNA repair","year":2015,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Epigenetics and DNA Methylation","field":"Biochemistry, Genetics and Molecular Biology","cited_by":451,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Université Laval; Centre hospitalier universitaire de Québec; Public Health Ontario; Lunenfeld-Tanenbaum Research Institute; Mount Sinai Hospital; McGill University; Royal Victoria Hospital; University of Toronto","funders":"National Center for Research Resources; National Institute of Diabetes and Digestive and Kidney Diseases; National Center for Advancing Translational Sciences; Wellcome Trust; National Human Genome Research Institute; National Institute on Drug Abuse; National Heart, Lung, and Blood Institute; National Institute on Aging; Medical Research Council; National Institute for Health and Care Research; National Cancer Institute; Cancer Research UK; National Institutes of Health; Francis Crick Institute","keywords":"Biology; Breast cancer; DNA repair; Genetics; DNA; Computational biology; Cancer research; Cancer","score_opus":0.019352107427071847,"score_gpt":0.31305160118015635,"score_spread":0.2936994937530845,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1904407543","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.92512554,0.045162905,0.014620931,0.006644379,0.0009294156,0.00011538894,0.0048079053,0.00026540307,0.0023281318],"genre_scores_gemma":[0.98424315,0.0068924925,0.004382188,0.0014628266,0.0004923792,0.000055774108,0.0010617074,0.00004859483,0.0013608887],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9993419,0.00020609183,0.000042664444,0.00025724186,0.00009337444,0.000058643982],"domain_scores_gemma":[0.99519783,0.0033864982,0.00048254052,0.00039960755,0.000313984,0.00021954032],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0017974244,0.0009774384,0.0006850084,0.001072244,0.00055900135,0.0009335584,0.0005539506,0.0008370976,0.0023988683],"category_scores_gemma":[0.0058189444,0.00037762392,0.0031026187,0.0011384934,0.0003781803,0.00023024181,0.0007398373,0.0011212266,0.00024110217],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.009159576,0.00025743208,0.79483384,0.0015158734,0.04288372,0.0029790096,0.00051217526,0.0030852999,0.037124082,0.0010658165,0.012462375,0.09412084],"study_design_scores_gemma":[0.0013735219,0.0011952162,0.8887119,0.00031332247,0.05476858,0.003562906,0.0003703411,0.006130471,0.014591729,0.0062599387,0.022567287,0.00015474565],"about_ca_topic_score_codex":0.004111175,"about_ca_topic_score_gemma":0.0075835623,"teacher_disagreement_score":0.004111175,"about_ca_system_score_codex":0.00037867617,"about_ca_system_score_gemma":0.0003634863,"threshold_uncertainty_score":0.009505808},"labels":[],"label_agreement":null},{"id":"W1916780560","doi":"10.1038/ng.3373","title":"Genome-wide meta-analysis identifies five new susceptibility loci for cutaneous malignant melanoma","year":2015,"lang":"en","type":"review","venue":"Nature Genetics","topic":"melanin and skin pigmentation","field":"Biochemistry, Genetics and Molecular Biology","cited_by":245,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"McGill University and Génome Québec Innovation Centre","funders":"National Center for Advancing Translational Sciences; Cancer Research UK; National Cancer Institute; Medical Research Council; Francis Crick Institute; Wellcome Trust","keywords":"Genome-wide association study; Biology; Expression quantitative trait loci; Genetics; Single-nucleotide polymorphism; Locus (genetics); Genetic association; Genome; Melanoma; Quantitative trait locus; Genetic architecture; Meta-analysis; Computational biology; Gene; Genotype; Pathology; Medicine","score_opus":0.05192433694363166,"score_gpt":0.34682943046210307,"score_spread":0.2949050935184714,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1916780560","genre_codex":"review","genre_gemma":"review","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"review","genre_consensus":"review","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.0066370443,0.9903736,0.00085405377,0.0009597092,0.000192336,0.000007291348,0.00042030742,0.00002355623,0.00053216063],"genre_scores_gemma":[0.07553757,0.9191231,0.001887367,0.0011232322,0.00063914695,0.00002293234,0.0010329223,0.000015342152,0.0006184742],"study_design_codex":"design_other","study_design_gemma":"meta_analysis","domain_scores_codex":[0.9996543,0.000085214655,0.00004595513,0.00011543152,0.00006959861,0.000029504721],"domain_scores_gemma":[0.9992526,0.0004936234,0.00010659886,0.00003513431,0.0000701601,0.000041861327],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0010853906,0.0009359444,0.0018262654,0.0010666817,0.00013421715,0.00081461115,0.00076484133,0.00084565993,0.0017603852],"category_scores_gemma":[0.0016514803,0.0002824552,0.0020359938,0.0016060278,0.0002032364,0.00038292966,0.0005972537,0.00086752337,0.00019040241],"study_design_candidate":"meta_analysis","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0015147979,0.000074891985,0.076270886,0.029053694,0.037709057,0.0021276802,0.0001534177,0.0016124387,0.0051277904,0.0025053327,0.027977714,0.8158723],"study_design_scores_gemma":[0.00089638133,0.0006834091,0.3801212,0.012681629,0.17993,0.011692666,0.00050946616,0.0024158643,0.003944885,0.017558703,0.38929683,0.0002690116],"about_ca_topic_score_codex":0.0015467722,"about_ca_topic_score_gemma":0.0048027164,"teacher_disagreement_score":0.0018262654,"about_ca_system_score_codex":0.00031694293,"about_ca_system_score_gemma":0.00069091114,"threshold_uncertainty_score":0.0058891177},"labels":[],"label_agreement":null},{"id":"W1963557285","doi":"10.1038/ng.2646","title":"Targeted resequencing in epileptic encephalopathies identifies de novo mutations in CHD2 and SYNGAP1","year":2013,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Genomics and Rare Diseases","field":"Biochemistry, Genetics and Molecular Biology","cited_by":694,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Toronto Western Hospital; University of Toronto","funders":"National Institute of Neurological Disorders and Stroke","keywords":"Biology; Cohort; Genetics; Phenotype; Mutation; Etiology; Epilepsy; Massive parallel sequencing; Gene; Medicine; DNA sequencing; Internal medicine; Neuroscience","score_opus":0.004760474058205903,"score_gpt":0.23972769984834563,"score_spread":0.23496722579013973,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1963557285","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99487793,0.0002866137,0.002872305,0.000119742566,0.000039218532,0.000030574578,0.00060063496,0.00006972595,0.0011031838],"genre_scores_gemma":[0.9971831,0.00013430443,0.0014965691,0.00007845234,0.000014543024,0.000014579616,0.00052857655,0.000027797398,0.000522266],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.99984145,0.00002219327,0.000022287697,0.000037023914,0.00005626221,0.000020700452],"domain_scores_gemma":[0.999772,0.00011903626,0.0000386564,0.000022461583,0.00001630698,0.000031586078],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00021769652,0.00052404107,0.00027026417,0.00077452033,0.00031579676,0.00030273866,0.00032749437,0.00066072075,0.001229297],"category_scores_gemma":[0.0005861343,0.00019915104,0.00039956454,0.00029651404,0.0002934358,0.00013686072,0.00030549278,0.00040116903,0.0003657401],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0005043994,0.00008167174,0.007220825,0.0000822798,0.00012654802,0.016259288,0.00021147622,0.0011382672,0.9650451,0.0006054101,0.0005710421,0.008153752],"study_design_scores_gemma":[0.00020610444,0.0004425906,0.14078063,0.000051691877,0.0004945837,0.08263447,0.0003630873,0.011483875,0.75297374,0.0010967345,0.009411641,0.00006080815],"about_ca_topic_score_codex":0.0006398524,"about_ca_topic_score_gemma":0.0016347138,"teacher_disagreement_score":0.001229297,"about_ca_system_score_codex":0.00022610968,"about_ca_system_score_gemma":0.00015273702,"threshold_uncertainty_score":0.004112363},"labels":[],"label_agreement":null},{"id":"W1963558153","doi":"10.1038/ng.294","title":"Identification of a putative lysosomal cobalamin exporter altered in the cblF defect of vitamin B12 metabolism","year":2009,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Folate and B Vitamins Research","field":"Medicine","cited_by":180,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"McGill University Health Centre","funders":"","keywords":"Cobalamin; Biology; Vitamin B12; Frameshift mutation; Biochemistry; Mutation; Gene","score_opus":0.013518078894584179,"score_gpt":0.3237733884409083,"score_spread":0.31025530954632413,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1963558153","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99576426,0.0002407031,0.0024875568,0.00022954342,0.000057113848,0.000018991463,0.00052853086,0.00011451406,0.00055889535],"genre_scores_gemma":[0.9975815,0.00006220026,0.0013519651,0.000049375474,0.000014642875,0.000006230936,0.00027791655,0.000034628447,0.00062151323],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9998319,0.000019677942,0.000034157085,0.000041552583,0.000038202863,0.000034341367],"domain_scores_gemma":[0.99947625,0.00014276025,0.00013286759,0.000052517313,0.00006695609,0.00012868873],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00014996118,0.00057076383,0.0006135026,0.0006497629,0.0004617993,0.00052084407,0.0006154795,0.00149345,0.0024855991],"category_scores_gemma":[0.0006862934,0.00018050945,0.0005921134,0.00030201307,0.0005832157,0.00028211364,0.0003858171,0.00067393965,0.0006331224],"study_design_candidate":"bench_or_experimental","study_design_consensus":"bench_or_experimental","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0009347165,0.00007740969,0.0048681526,0.00006702165,0.000053119704,0.02226793,0.000086723434,0.00034613354,0.9673104,0.0004886663,0.00023027323,0.0032693627],"study_design_scores_gemma":[0.00013650088,0.00039713967,0.03282293,0.000029058809,0.00018639478,0.060124833,0.00023309505,0.004934279,0.89632076,0.0005841323,0.004170497,0.00006034795],"about_ca_topic_score_codex":0.0015371821,"about_ca_topic_score_gemma":0.00073630223,"teacher_disagreement_score":0.0024855991,"about_ca_system_score_codex":0.000515002,"about_ca_system_score_gemma":0.0002871258,"threshold_uncertainty_score":0.008315146},"labels":[],"label_agreement":null},{"id":"W1964268435","doi":"10.1038/ng.2496","title":"Mutations in GNAL cause primary torsion dystonia","year":2012,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Neurological disorders and treatments","field":"Medicine","cited_by":322,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Toronto Western Hospital","funders":"National Institute of Neurological Disorders and Stroke; Bachmann-Strauss Dystonia and Parkinson Foundation; National Heart, Lung, and Blood Institute; National Institute on Drug Abuse; Agence Nationale de la Recherche; Parkinsonfonden; Universidade de São Paulo","keywords":"Missense mutation; Nonsense mutation; Biology; Genetics; Gene; Dystonia; Exome sequencing; Nonsense; Mutation; Neuroscience","score_opus":0.014337328526895165,"score_gpt":0.29246363389200924,"score_spread":0.27812630536511407,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1964268435","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9529718,0.003582029,0.0072445734,0.004738123,0.0013663941,0.000138274,0.0029992391,0.00088266144,0.026076742],"genre_scores_gemma":[0.99137974,0.0004511138,0.0030842868,0.0006094821,0.0002092974,0.000022427572,0.00046462566,0.0001506564,0.0036283568],"study_design_codex":"case_report","study_design_gemma":"observational","domain_scores_codex":[0.99964976,0.00006408742,0.00004158933,0.000073169125,0.000110927525,0.000060399463],"domain_scores_gemma":[0.9992373,0.00026763728,0.00023656328,0.000037359423,0.000039267023,0.00018180175],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0002105375,0.0017745416,0.00076566427,0.0015348011,0.0008769367,0.00076380675,0.0010013536,0.0033427973,0.011761859],"category_scores_gemma":[0.0012824758,0.00032987996,0.0007665674,0.0010542058,0.0018844949,0.0005497029,0.0013147477,0.0010009854,0.0016278481],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0016714444,0.00020483467,0.017691096,0.00046051908,0.00038707542,0.5582183,0.00068102183,0.002287129,0.36630952,0.007764267,0.0078050205,0.036519706],"study_design_scores_gemma":[0.0009386555,0.00079343264,0.12815684,0.00064389297,0.0009930179,0.6987058,0.0012371166,0.008060696,0.11686452,0.0068883337,0.036392596,0.0003251546],"about_ca_topic_score_codex":0.0023640392,"about_ca_topic_score_gemma":0.0042604716,"teacher_disagreement_score":0.011761859,"about_ca_system_score_codex":0.0010912077,"about_ca_system_score_gemma":0.0006385856,"threshold_uncertainty_score":0.03934741},"labels":[],"label_agreement":null},{"id":"W1964599358","doi":"10.1038/ng2000","title":"Stepwise replication identifies a low-producing lymphotoxin-α allele as a major risk factor for early-onset leprosy","year":2007,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Leprosy Research and Treatment","field":"Medicine","cited_by":168,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"McGill University","funders":"","keywords":"Linkage disequilibrium; Biology; Genetics; Leprosy; Odds ratio; Allele; Lymphotoxin alpha; Haplotype; Case-control study; Immunology; Internal medicine; Gene; Lymphotoxin; Medicine","score_opus":0.015296353633949334,"score_gpt":0.33498977374492644,"score_spread":0.3196934201109771,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1964599358","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99768186,0.0001331987,0.001209795,0.00009976693,0.000032244385,0.00002311492,0.00012269997,0.000023222969,0.00067415775],"genre_scores_gemma":[0.99802005,0.00005570732,0.0006803915,0.00007881423,0.000040369934,0.000010209347,0.00014292744,0.00003082918,0.0009407782],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.99937326,0.00023840292,0.000060840674,0.00013253791,0.00008964407,0.000105394494],"domain_scores_gemma":[0.9967932,0.0015372423,0.00048121405,0.0005117858,0.0003267255,0.00034974728],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0009341897,0.0005414072,0.00055632985,0.0011256605,0.00050617184,0.0006190723,0.00069598487,0.0008378952,0.0047793034],"category_scores_gemma":[0.0033739032,0.00029378262,0.0006427412,0.0006496422,0.0003705291,0.0003099733,0.00038984904,0.0012476067,0.0009446281],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0046227938,0.0005842293,0.47534755,0.00007607247,0.00019792157,0.010965951,0.00067201274,0.00015010928,0.49264237,0.0006206235,0.0003472615,0.013773147],"study_design_scores_gemma":[0.00021672784,0.0026499194,0.9356396,0.000041916835,0.00029118036,0.021270791,0.00048807985,0.0013004036,0.035749312,0.0007365454,0.0015721453,0.00004345322],"about_ca_topic_score_codex":0.0009929518,"about_ca_topic_score_gemma":0.00055597944,"teacher_disagreement_score":0.0047793034,"about_ca_system_score_codex":0.00014198112,"about_ca_system_score_gemma":0.0002457483,"threshold_uncertainty_score":0.01598841},"labels":[],"label_agreement":null},{"id":"W1964690949","doi":"10.1038/ng.242","title":"Disruption of an AP-2α binding site in an IRF6 enhancer is associated with cleft lip","year":2008,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Cleft Lip and Palate Research","field":"Biochemistry, Genetics and Molecular Biology","cited_by":427,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Ottawa","funders":"National Institute of Dental and Craniofacial Research; National Institute of Environmental Health Sciences; National Cancer Institute; National Institutes of Health; European Commission; National Human Genome Research Institute; National Center for Research Resources; American Heart Association; U.S. Department of Energy","keywords":"Enhancer; Biology; Allele; Craniofacial; Genetics; Transcription factor; SNP; Genotype; Single-nucleotide polymorphism; Binding site; Gene","score_opus":0.014447637672228375,"score_gpt":0.30519312830097,"score_spread":0.2907454906287416,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1964690949","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.985333,0.0006982037,0.0108839,0.00033686604,0.00018603296,0.00008441238,0.0007739895,0.0003918094,0.0013118534],"genre_scores_gemma":[0.9938543,0.00017406755,0.0032881964,0.00012508463,0.000032161483,0.000041202886,0.0005935488,0.00014230765,0.0017492282],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9994417,0.000115432056,0.00010261659,0.000110404435,0.00013795818,0.000091902584],"domain_scores_gemma":[0.9986576,0.00034011013,0.0005247558,0.00015366852,0.00004952466,0.0002743804],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00037827855,0.0006744598,0.0006405892,0.0010660427,0.0004427875,0.0004204894,0.0012661333,0.0012161244,0.0053649065],"category_scores_gemma":[0.00057664304,0.0005567043,0.0011587125,0.00039238576,0.001037862,0.00022091746,0.00093029614,0.0024166715,0.0021928414],"study_design_candidate":"bench_or_experimental","study_design_consensus":"bench_or_experimental","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0003819164,0.000112431575,0.0004229371,0.00004644734,0.000034155557,0.0010272135,0.000032373253,0.00017040133,0.9962674,0.00024822418,0.00009542326,0.001161058],"study_design_scores_gemma":[0.00029204923,0.0003322917,0.025658555,0.000068312904,0.00015835057,0.012175029,0.00017985667,0.003848734,0.9527517,0.00060461374,0.0038651258,0.000065472785],"about_ca_topic_score_codex":0.00077396695,"about_ca_topic_score_gemma":0.0009232637,"teacher_disagreement_score":0.0053649065,"about_ca_system_score_codex":0.0004605743,"about_ca_system_score_gemma":0.0002933239,"threshold_uncertainty_score":0.017947376},"labels":[],"label_agreement":null},{"id":"W1965619867","doi":"10.1038/ng1221","title":"Mutations in ENPP1 are associated with 'idiopathic' infantile arterial calcification","year":2003,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Alkaline Phosphatase Research Studies","field":"Medicine","cited_by":603,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Children's & Women's Health Centre of British Columbia","funders":"Deutsche Forschungsgemeinschaft; Arthritis National Research Foundation; U.S. Department of Veterans Affairs; National Institute for Health and Care Research; Foundation for the National Institutes of Health","keywords":"Calcification; Biology; Phosphodiesterase; Mutation; Pyrophosphate; Pyrophosphatase; Internal elastic lamina; Cell; Internal medicine; Endocrinology; Enzyme; Genetics; Biochemistry; Anatomy; Gene; Medicine; Smooth muscle","score_opus":0.016600301371038666,"score_gpt":0.3176670123914281,"score_spread":0.3010667110203894,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1965619867","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.992203,0.0009032662,0.0011455041,0.00046616417,0.00009985096,0.000028963277,0.00028555896,0.00010155307,0.004766231],"genre_scores_gemma":[0.9974865,0.00027281113,0.00078995904,0.000083244515,0.0001424906,0.000013073022,0.0001447389,0.00003416319,0.0010329193],"study_design_codex":"case_report","study_design_gemma":"observational","domain_scores_codex":[0.99925023,0.00012133388,0.00011762124,0.00015655896,0.0002233935,0.00013094171],"domain_scores_gemma":[0.99679476,0.0016276019,0.0008982036,0.00016769342,0.00017806426,0.00033360856],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00047495004,0.0021823458,0.0009672371,0.0028477693,0.00081828824,0.0006333747,0.0012935288,0.0031435606,0.004547096],"category_scores_gemma":[0.0052203136,0.00064032676,0.000532699,0.0019360469,0.0016932655,0.00067783217,0.00088963023,0.0012747304,0.00070725166],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0012995467,0.00022615214,0.057582103,0.00024825946,0.00016858322,0.8621319,0.0013681651,0.00068109983,0.06441895,0.0012349114,0.001205656,0.009434642],"study_design_scores_gemma":[0.00011764177,0.00027765,0.11899835,0.00006847165,0.0002633168,0.84938174,0.0004130678,0.0013884597,0.024475118,0.0007457971,0.0038158854,0.000054469085],"about_ca_topic_score_codex":0.001229167,"about_ca_topic_score_gemma":0.0008567007,"teacher_disagreement_score":0.004547096,"about_ca_system_score_codex":0.00032449092,"about_ca_system_score_gemma":0.00031139623,"threshold_uncertainty_score":0.015211523},"labels":[],"label_agreement":null},{"id":"W1965857060","doi":"10.1038/ng.2932","title":"Global optimization of somatic variant identification in cancer genomes with a global community challenge","year":2014,"lang":"en","type":"letter","venue":"Nature Genetics","topic":"Cancer Genomics and Diagnostics","field":"Biochemistry, Genetics and Molecular Biology","cited_by":46,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Toronto; Ontario Institute for Cancer Research","funders":"National Cancer Institute","keywords":"Biology; Somatic cell; Identification (biology); Genome; Computational biology; Genetics; Cancer; Gene; Ecology","score_opus":0.009970225511434937,"score_gpt":0.26395814968343606,"score_spread":0.2539879241720011,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1965857060","genre_codex":"commentary","genre_gemma":"methods","domain_codex":null,"domain_gemma":"methods","model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"methods","genre_consensus":null,"domain_candidate":"methods","domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.0282855,0.0096192015,0.08977894,0.84514886,0.013860629,0.00008014156,0.00052659033,0.00082643813,0.011873689],"genre_scores_gemma":[0.45179996,0.0069479565,0.10960257,0.38763997,0.025471969,0.0003132233,0.00061983237,0.0006619141,0.016942594],"study_design_codex":"not_applicable","study_design_gemma":"simulation_or_modeling","domain_scores_codex":[0.99792814,0.00088505965,0.00008207142,0.0002866807,0.00059427513,0.00022378388],"domain_scores_gemma":[0.9918053,0.0061601643,0.00027399193,0.00040711695,0.00093614525,0.0004172614],"candidate_categories":["metaresearch"],"consensus_categories":[],"category_scores_codex":[0.004412706,0.00050276425,0.0012626306,0.00024737694,0.0008364162,0.0016356106,0.0012168161,0.0055428343,0.0026787897],"category_scores_gemma":[0.014589123,0.00039885478,0.0008845996,0.00043764178,0.0014573538,0.0017690876,0.0012599672,0.007234917,0.0012499248],"study_design_candidate":"simulation_or_modeling","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0014786308,0.00036936294,0.0048918384,0.00031091602,0.0002703001,0.0026268011,0.0001701456,0.06524678,0.014658241,0.0392666,0.6289539,0.24175659],"study_design_scores_gemma":[0.000957505,0.00063388393,0.004956003,0.00016745311,0.00019676943,0.00391158,0.0005787027,0.2626375,0.021631215,0.23175977,0.47236967,0.00019993671],"about_ca_topic_score_codex":0.0018222982,"about_ca_topic_score_gemma":0.0036901748,"teacher_disagreement_score":0.9955873,"about_ca_system_score_codex":0.0016318611,"about_ca_system_score_gemma":0.0010053646,"threshold_uncertainty_score":0.023336947},"labels":[],"label_agreement":null},{"id":"W1965888676","doi":"10.1038/ng.3065","title":"Human somatic cell mutagenesis creates genetically tractable sarcomas","year":2014,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Virus-based gene therapy research","field":"Biochemistry, Genetics and Molecular Biology","cited_by":28,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Mount Sinai Hospital; University of Toronto; Ontario Institute for Cancer Research","funders":"Canadian Institutes of Health Research","keywords":"Biology; Insertional mutagenesis; Transposable element; Somatic cell; Genetics; Germline; Mutagenesis; Gene; Genome; Computational biology; Retrotransposon; Mutation","score_opus":0.008950418987346418,"score_gpt":0.2841832261376065,"score_spread":0.27523280715026005,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1965888676","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.95998687,0.00083483674,0.030114647,0.00023541298,0.00012608033,0.00016298247,0.00090317836,0.00046647212,0.00716956],"genre_scores_gemma":[0.9860036,0.000627819,0.008170904,0.000044639157,0.000014045261,0.000032111067,0.00041318068,0.0000978639,0.0045958837],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99981123,0.000045288445,0.00001895936,0.00003139715,0.00006148471,0.00003169483],"domain_scores_gemma":[0.9998148,0.00006193141,0.00005082571,0.000033110035,0.000010605234,0.00002873727],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00028389797,0.00040016757,0.00023219062,0.00048656465,0.00014169508,0.00030795057,0.00025159807,0.0003897796,0.0022404322],"category_scores_gemma":[0.00023367885,0.00023746995,0.00024910187,0.00023548177,0.00037866947,0.00017810328,0.00030297108,0.00051014265,0.0007075436],"study_design_candidate":"bench_or_experimental","study_design_consensus":"bench_or_experimental","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.000059981245,0.00002235047,0.00014316836,0.000018514866,0.000008322589,0.00010158898,0.000021040843,0.00031910912,0.99475515,0.002752353,0.00007541457,0.001723006],"study_design_scores_gemma":[0.000023125034,0.00012634169,0.00080660783,0.000005139423,0.000020438272,0.00059166254,0.000020227148,0.0015450744,0.99076957,0.00043613877,0.0056497497,0.0000059009253],"about_ca_topic_score_codex":0.0004983651,"about_ca_topic_score_gemma":0.00070157147,"teacher_disagreement_score":0.0022404322,"about_ca_system_score_codex":0.0002672789,"about_ca_system_score_gemma":0.00023842212,"threshold_uncertainty_score":0.0074949265},"labels":[],"label_agreement":null},{"id":"W1966292963","doi":"10.1038/ng.2356","title":"Mutations in NMNAT1 cause Leber congenital amaurosis and identify a new disease pathway for retinal degeneration","year":2012,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Retinal Development and Disorders","field":"Biochemistry, Genetics and Molecular Biology","cited_by":205,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"McGill University; McGill University and Génome Québec Innovation Centre; McGill University Health Centre","funders":"National Center for Research Resources; National Eye Institute; Canadian Institutes of Health Research; U.S. Department of Veterans Affairs","keywords":"Biology; Retinal degeneration; Genetics; Wallerian degeneration; Exome sequencing; Retinitis pigmentosa; Gene; Mutation; Neuroscience","score_opus":0.011762978080074721,"score_gpt":0.27890946096530755,"score_spread":0.26714648288523285,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1966292963","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9778234,0.0034597996,0.009682412,0.0016575921,0.0005475848,0.000046028592,0.00065085094,0.00036562493,0.0057665887],"genre_scores_gemma":[0.9901536,0.0011267953,0.0066164173,0.00018536187,0.00006544228,0.000023895785,0.0002555441,0.00005989603,0.0015130837],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9997764,0.000027717702,0.000031521035,0.000049277467,0.00008842537,0.000026636058],"domain_scores_gemma":[0.9996165,0.000096748096,0.00013177896,0.000022410657,0.000041157407,0.00009143387],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00026324307,0.0010585523,0.0004839173,0.0009582302,0.000570272,0.0006734892,0.0005639604,0.001414684,0.0015719472],"category_scores_gemma":[0.00082755066,0.00033141128,0.0004171503,0.00030425514,0.00083536207,0.00063894386,0.0006478865,0.0006759704,0.000491768],"study_design_candidate":"bench_or_experimental","study_design_consensus":"bench_or_experimental","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0008058261,0.00005775399,0.01701182,0.00015830142,0.00009085831,0.039984617,0.00021964396,0.0010448417,0.92035747,0.0059236865,0.001696074,0.012649182],"study_design_scores_gemma":[0.00020611625,0.00038912636,0.08802584,0.00012552655,0.00033052452,0.15452772,0.00044754308,0.012848961,0.70847684,0.008301041,0.026152492,0.00016821659],"about_ca_topic_score_codex":0.0013708534,"about_ca_topic_score_gemma":0.0025693583,"teacher_disagreement_score":0.0015719472,"about_ca_system_score_codex":0.0008109323,"about_ca_system_score_gemma":0.00038278624,"threshold_uncertainty_score":0.0058837533},"labels":[],"label_agreement":null},{"id":"W1966831629","doi":"10.1038/ng.801","title":"Common variants at MS4A4/MS4A6E, CD2AP, CD33 and EPHA1 are associated with late-onset Alzheimer's disease","year":2011,"lang":"en","type":"review","venue":"Nature Genetics","topic":"Alzheimer's disease research and treatments","field":"Medicine","cited_by":2014,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Occupational Cancer Research Centre; University of Toronto","funders":"National Cancer Institute; National Human Genome Research Institute; National Institute on Aging; National Center for Research Resources; National Institute of Neurological Disorders and Stroke; National Institute of Mental Health; Medical Research Council; Canadian Institutes of Health Research; Wellcome Trust; Howard Hughes Medical Institute","keywords":"Genome-wide association study; Biology; Meta-analysis; Alzheimer's disease; Disease; Genetics; Internal medicine; Single-nucleotide polymorphism; Genotype; Medicine; Gene","score_opus":0.04900553444875955,"score_gpt":0.34441351991947045,"score_spread":0.2954079854707109,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1966831629","genre_codex":"review","genre_gemma":"review","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"review","genre_consensus":"review","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.0008213096,0.9974318,0.0002387772,0.00033499618,0.00014020359,0.000005140842,0.00006424101,0.000009228619,0.0009543203],"genre_scores_gemma":[0.0035036914,0.99423003,0.0006420311,0.00023243601,0.00021024453,0.00000804687,0.00015906485,0.0000024625429,0.0010119365],"study_design_codex":"design_other","study_design_gemma":"observational","domain_scores_codex":[0.999877,0.000017803146,0.000024462219,0.000025162837,0.000044672415,0.000010943188],"domain_scores_gemma":[0.9998099,0.000090283334,0.000040683528,0.0000046217724,0.000041269144,0.000013275594],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0003953895,0.00081493874,0.001208033,0.0010141728,0.0001385571,0.0003984396,0.00061949197,0.0005572031,0.0019567022],"category_scores_gemma":[0.00048355747,0.00018160397,0.00039496398,0.0011790247,0.00023425418,0.00040079022,0.00032360674,0.00071908126,0.0006889799],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00019402544,0.000038231712,0.0015124218,0.007184421,0.00036352858,0.00058410346,0.000025707883,0.00030712152,0.0027062767,0.001167526,0.020436972,0.9654798],"study_design_scores_gemma":[0.00016232672,0.00013503163,0.013631742,0.0042603095,0.0015533118,0.008792968,0.00011029066,0.00022779212,0.0019474853,0.003949962,0.96518695,0.000041684416],"about_ca_topic_score_codex":0.0018420395,"about_ca_topic_score_gemma":0.004388872,"teacher_disagreement_score":0.0019567022,"about_ca_system_score_codex":0.0003375151,"about_ca_system_score_gemma":0.00060816406,"threshold_uncertainty_score":0.0065458417},"labels":[],"label_agreement":null},{"id":"W1967291345","doi":"10.1038/ng849","title":"Germline mutations in FH predispose to dominantly inherited uterine fibroids, skin leiomyomata and papillary renal cell cancer","year":2002,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Renal cell carcinoma treatment","field":"Medicine","cited_by":1634,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Hatch (Canada)","funders":"U.S. Public Health Service","keywords":"Biology; Cancer research; Genetics; Germline mutation; Compound heterozygosity; Mutation; Pathogenesis; Germline; Fumarase; Gene; Immunology","score_opus":0.014137535375178496,"score_gpt":0.28032798266857306,"score_spread":0.2661904472933946,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1967291345","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9905098,0.00080986373,0.0013297139,0.0004269661,0.000047718597,0.00002279913,0.00019802626,0.000084079016,0.0065710633],"genre_scores_gemma":[0.99832827,0.0001594671,0.0003699541,0.000049085444,0.000042652315,0.0000030483616,0.00004022984,0.000012059045,0.0009952737],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.999778,0.0000546071,0.000017753237,0.00004832747,0.000053621017,0.000047720638],"domain_scores_gemma":[0.9995703,0.0002096259,0.0000893316,0.00002537634,0.000023475564,0.00008178328],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00019602223,0.0005880982,0.00027960306,0.0012778303,0.000535536,0.00027765083,0.00026401877,0.0007871636,0.0063484316],"category_scores_gemma":[0.0011319342,0.00019350483,0.00032721972,0.0005487007,0.00050457707,0.00019092164,0.0002970851,0.0004311549,0.00030634497],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0029033017,0.0004389111,0.29739296,0.00021416087,0.0003944848,0.27353778,0.0012078998,0.0009488548,0.36915764,0.0062657753,0.002550059,0.044988185],"study_design_scores_gemma":[0.00019307566,0.0006963293,0.46907562,0.00005211295,0.000445144,0.48531052,0.0006445031,0.002250437,0.03329946,0.0024143872,0.005559306,0.000059115835],"about_ca_topic_score_codex":0.0019025457,"about_ca_topic_score_gemma":0.0022817042,"teacher_disagreement_score":0.0063484316,"about_ca_system_score_codex":0.00021160714,"about_ca_system_score_gemma":0.0002750527,"threshold_uncertainty_score":0.021237612},"labels":[],"label_agreement":null},{"id":"W1967546787","doi":"10.1038/ng1002","title":"The K–Cl cotransporter KCC3 is mutant in a severe peripheral neuropathy associated with agenesis of the corpus callosum","year":2002,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Metabolism and Genetic Disorders","field":"Biochemistry, Genetics and Molecular Biology","cited_by":278,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Cégep de Chicoutimi; McGill University; Hôpital de l'Enfant-Jésus; Montreal General Hospital","funders":"","keywords":"Agenesis of the corpus callosum; Biology; Genetics; Mutation; Agenesis; Xenopus; Corpus callosum; Population; Mutant; Missense mutation; Anatomy; Gene; Medicine","score_opus":0.005056066925170922,"score_gpt":0.1971182872773316,"score_spread":0.1920622203521607,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1967546787","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99663806,0.00029203945,0.0011951029,0.0003027852,0.00009440586,0.000032079355,0.00034275165,0.00012483222,0.0009779565],"genre_scores_gemma":[0.9978193,0.00014948242,0.00093444035,0.000089109235,0.000034251392,0.00001628853,0.00014393376,0.00005701898,0.00075613876],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.999597,0.0000701521,0.00007998414,0.000085400214,0.00009938896,0.0000681007],"domain_scores_gemma":[0.99885345,0.00028901728,0.00033778235,0.00006225618,0.00007776273,0.0003797427],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.000314776,0.002072253,0.0008353067,0.0010886634,0.0011809764,0.0004845887,0.0009288485,0.0022504644,0.0020847279],"category_scores_gemma":[0.0010472698,0.00041904167,0.000709381,0.00073465233,0.002111002,0.0003443512,0.00089454657,0.0017080456,0.00049254677],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0025905785,0.00026774258,0.004603624,0.00024318819,0.00026874346,0.25071445,0.00048445753,0.001340623,0.7320319,0.0011794254,0.0009967996,0.0052785138],"study_design_scores_gemma":[0.0009057872,0.0013885327,0.107563674,0.00020198706,0.0010152964,0.5454237,0.0009326258,0.009462192,0.3250221,0.0022613204,0.0055134105,0.0003093535],"about_ca_topic_score_codex":0.0057767318,"about_ca_topic_score_gemma":0.0045122146,"teacher_disagreement_score":0.0057767318,"about_ca_system_score_codex":0.00070557,"about_ca_system_score_gemma":0.0007886047,"threshold_uncertainty_score":0.011486232},"labels":[],"label_agreement":null},{"id":"W1967724489","doi":"10.1038/ng1647","title":"A predominant role for the HLA class II region in the association of the MHC region with multiple sclerosis","year":2005,"lang":"en","type":"article","venue":"Nature Genetics","topic":"T-cell and B-cell Immunology","field":"Immunology and Microbiology","cited_by":333,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of British Columbia; McGill University and Génome Québec Innovation Centre; McGill University Health Centre","funders":"","keywords":"Genetics; Biology; Major histocompatibility complex; Human leukocyte antigen; Haplotype; Multiple sclerosis; Allele; Locus (genetics); SNP; Single-nucleotide polymorphism; MHC class I; MHC class II; Gene; Genetic association; Genotype; Immunology; Antigen","score_opus":0.010792361513214067,"score_gpt":0.20448422256343018,"score_spread":0.19369186105021613,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1967724489","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9888387,0.004904173,0.0026596694,0.000265297,0.00006256661,0.0000070540586,0.000100077705,0.000035721125,0.003126689],"genre_scores_gemma":[0.99768925,0.0008183297,0.0005735903,0.000076542616,0.000084689724,0.0000027163976,0.000046135818,0.000011254217,0.00069747],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.99978,0.00006217923,0.000024155615,0.00006697842,0.000028957395,0.00003766947],"domain_scores_gemma":[0.9994142,0.00018735725,0.00012763405,0.00009784362,0.00008410357,0.00008889362],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00045606063,0.00016470824,0.00022313281,0.00038144115,0.0002620736,0.00036439515,0.00026237563,0.000419877,0.003608731],"category_scores_gemma":[0.00076754246,0.00009606476,0.00016826243,0.00026416656,0.00029664807,0.00023080054,0.00025567395,0.00038054673,0.00065560476],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.001909688,0.000048244106,0.056987338,0.00017554307,0.00010004174,0.002023893,0.00020955625,0.0001559775,0.9159666,0.0015438342,0.00028451256,0.020594833],"study_design_scores_gemma":[0.00023266912,0.0017649654,0.7209508,0.00015182621,0.0005085959,0.054149467,0.0008276282,0.001446681,0.19995111,0.0034628229,0.01651177,0.000041677697],"about_ca_topic_score_codex":0.00043325426,"about_ca_topic_score_gemma":0.00033102353,"teacher_disagreement_score":0.003608731,"about_ca_system_score_codex":0.000107684216,"about_ca_system_score_gemma":0.00015754347,"threshold_uncertainty_score":0.012072444},"labels":[],"label_agreement":null},{"id":"W1967917209","doi":"10.1038/ng.2245","title":"Common variants at 6q22 and 17q21 are associated with intracranial volume","year":2012,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Genomic variations and chromosomal abnormalities","field":"Biochemistry, Genetics and Molecular Biology","cited_by":144,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Toronto; Ontario Institute for Cancer Research","funders":"Eunice Kennedy Shriver National Institute of Child Health and Human Development; National Center for Research Resources; National Institute of Neurological Disorders and Stroke; National Institute of Mental Health; National Heart, Lung, and Blood Institute; Medical Research Council; Canadian Institutes of Health Research; National Institutes of Health; Austrian Science Fund; Raine Medical Research Foundation; ZonMw; National Institute on Aging; Medizinische Universität Graz; University of Bristol; Healthway; National Human Genome Research Institute; Wellcome Trust; National Health and Medical Research Council; Children's Hospital of Philadelphia","keywords":"Brain size; Locus (genetics); Genome-wide association study; Biology; Genetics; Single-nucleotide polymorphism; Medicine; Gene; Genotype","score_opus":0.0048104717881907915,"score_gpt":0.20736203455404276,"score_spread":0.20255156276585196,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1967917209","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99620676,0.0009825447,0.0006672691,0.00017707821,0.000031568008,0.000012202978,0.00088725536,0.00007744707,0.00095772644],"genre_scores_gemma":[0.9976573,0.00042787887,0.0006051913,0.000022255792,0.00008020445,0.000011410254,0.0006098413,0.000036580044,0.00054943067],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99938893,0.00008493617,0.00007567964,0.00015746811,0.0002026011,0.000090299305],"domain_scores_gemma":[0.99684227,0.0008426073,0.0017993306,0.00015228464,0.0001272967,0.00023619532],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00030340787,0.0014394432,0.0009558116,0.0037910107,0.0005146028,0.0007685749,0.0011646631,0.00114222,0.006068358],"category_scores_gemma":[0.0026469824,0.0005326066,0.0010006488,0.0039099306,0.00085821585,0.0004299296,0.0007358449,0.00090663397,0.0004345516],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0037277108,0.00017172327,0.75829786,0.00026895374,0.0012622733,0.0730646,0.0009170858,0.0015906248,0.13385615,0.0012649256,0.0015005928,0.024077501],"study_design_scores_gemma":[0.00005872938,0.00014049243,0.94225967,0.00002959335,0.00045533656,0.04820455,0.00017489049,0.0007182018,0.0060712267,0.0009443601,0.0009001591,0.000042710402],"about_ca_topic_score_codex":0.0032187707,"about_ca_topic_score_gemma":0.0023010033,"teacher_disagreement_score":0.006068358,"about_ca_system_score_codex":0.0003294522,"about_ca_system_score_gemma":0.00043786067,"threshold_uncertainty_score":0.020300627},"labels":[],"label_agreement":null},{"id":"W1968214033","doi":"10.1038/ng.3165","title":"BAZ2A (TIP5) is involved in epigenetic alterations in prostate cancer and its overexpression predicts disease recurrence","year":2014,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Epigenetics and DNA Methylation","field":"Biochemistry, Genetics and Molecular Biology","cited_by":151,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Toronto","funders":"Swiss Cancer Research Foundation; Federalno Ministarstvo Obrazovanja i Nauke; Wellcome Trust; Deutsches Krebsforschungszentrum; Mäxi-Stiftung; Schweizerischer Nationalfonds zur Förderung der Wissenschaftlichen Forschung; National Science Foundation","keywords":"Epigenetics; Prostate cancer; Biology; Gene silencing; EZH2; Cancer research; Cancer; Chromoplexy; Genetics; Gene; PCA3","score_opus":0.009302377633928473,"score_gpt":0.27908164884180847,"score_spread":0.26977927120788,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1968214033","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9904122,0.005271265,0.001490853,0.00030843256,0.000049173264,0.000016099806,0.001043693,0.00009462174,0.0013136809],"genre_scores_gemma":[0.99779785,0.0005771237,0.0003764387,0.00004424935,0.000012074693,0.0000077998,0.0005564982,0.000010572561,0.0006174271],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9997967,0.00002952049,0.000013844226,0.000041328738,0.000084723135,0.000033959215],"domain_scores_gemma":[0.999708,0.000033081757,0.00014393279,0.000020575357,0.000032672528,0.00006170486],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00020906879,0.00023318453,0.00025174447,0.00074586016,0.0003022458,0.0005492577,0.00030653022,0.00041361133,0.0020967117],"category_scores_gemma":[0.0004999974,0.00022013864,0.00034058906,0.0007972813,0.00022976768,0.00018511839,0.00038995073,0.0004350255,0.0004841565],"study_design_candidate":"bench_or_experimental","study_design_consensus":"bench_or_experimental","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.002246146,0.00009413967,0.3821548,0.0002471457,0.000611974,0.0017884269,0.000094666975,0.0009038848,0.57670826,0.0006322683,0.0025096552,0.03200859],"study_design_scores_gemma":[0.00006554669,0.00020101827,0.8929036,0.00001950536,0.00041197406,0.006639287,0.00015987357,0.0035799535,0.087629884,0.0005614529,0.007803045,0.000024814477],"about_ca_topic_score_codex":0.0013787866,"about_ca_topic_score_gemma":0.0013479815,"teacher_disagreement_score":0.0020967117,"about_ca_system_score_codex":0.00031735867,"about_ca_system_score_gemma":0.00019656536,"threshold_uncertainty_score":0.007014215},"labels":[],"label_agreement":null},{"id":"W1968344288","doi":"10.1038/ng.580","title":"A genome-wide association study of cleft lip with and without cleft palate identifies risk variants near MAFB and ABCA4","year":2010,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Cleft Lip and Palate Research","field":"Biochemistry, Genetics and Molecular Biology","cited_by":594,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of British Columbia","funders":"Eunice Kennedy Shriver National Institute of Child Health and Human Development; National Institute of Dental and Craniofacial Research; National Institute of Arthritis and Musculoskeletal and Skin Diseases; National Human Genome Research Institute; Canadian Institutes of Health Research; Johns Hopkins University; University of Pittsburgh; National Institutes of Health; March of Dimes Foundation; National University of Singapore; U.S. Public Health Service; Utah State University","keywords":"ABCA4; Biology; Genome-wide association study; Genetics; Odds ratio; Single-nucleotide polymorphism; Genetic association; Allele; SNP; Minor allele frequency; Gene; Genotype; Internal medicine; Medicine; Phenotype","score_opus":0.005789614267260837,"score_gpt":0.26353731289396815,"score_spread":0.2577476986267073,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1968344288","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99832326,0.00040238193,0.000524362,0.00011840995,0.00002205462,0.000007445859,0.00021752188,0.00002281525,0.00036179353],"genre_scores_gemma":[0.99907327,0.000084574596,0.00030365068,0.000031466265,0.00001343243,0.0000065354902,0.00012862703,0.000011356357,0.0003468782],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9990038,0.00027867028,0.00011219317,0.00033839623,0.00014272219,0.00012429303],"domain_scores_gemma":[0.9983746,0.0007699827,0.00029139637,0.00024242146,0.000119013705,0.00020262838],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0011849891,0.00084525754,0.000738355,0.0017234243,0.00092770316,0.00088418415,0.0007874367,0.0012490078,0.0037717693],"category_scores_gemma":[0.0028713034,0.00061293767,0.0015263705,0.0013770484,0.0008226246,0.00033685338,0.00091475615,0.0012357326,0.00031799136],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.010851712,0.00039991466,0.85705674,0.00013722148,0.004511603,0.004865367,0.0009173586,0.00036680436,0.10869502,0.0006598756,0.00091928407,0.010619096],"study_design_scores_gemma":[0.00043219692,0.00037188712,0.9859642,0.000025858582,0.002301834,0.005299227,0.00035390866,0.0009790267,0.0031025666,0.0003952599,0.0007371639,0.000036901223],"about_ca_topic_score_codex":0.007443495,"about_ca_topic_score_gemma":0.0057078744,"teacher_disagreement_score":0.007443495,"about_ca_system_score_codex":0.00029487108,"about_ca_system_score_gemma":0.0003510674,"threshold_uncertainty_score":0.01480031},"labels":[],"label_agreement":null},{"id":"W1970006069","doi":"10.1038/ng.626","title":"Genome-wide association study of follicular lymphoma identifies a risk locus at 6p21.32","year":2010,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Chronic Lymphocytic Leukemia Research","field":"Medicine","cited_by":157,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of British Columbia; Simon Fraser University; BC Cancer Agency","funders":"National Institute of Environmental Health Sciences; National Cancer Institute","keywords":"Follicular lymphoma; Biology; Chronic lymphocytic leukemia; Lymphoma; Genome-wide association study; Genetic association; Locus (genetics); Genetics; Leukemia; Single-nucleotide polymorphism; Immunology; Gene; Genotype","score_opus":0.007304496344641298,"score_gpt":0.2810534068355785,"score_spread":0.2737489104909372,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1970006069","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99466234,0.0011055096,0.0014543566,0.0005727495,0.000041441624,0.000023771025,0.0007394317,0.00007519383,0.001325115],"genre_scores_gemma":[0.99736017,0.0003024999,0.0007559884,0.00006424939,0.00004581164,0.000017769751,0.000516627,0.000014677595,0.0009221134],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.999469,0.00019039129,0.000034902707,0.00012640303,0.00011293271,0.000066347806],"domain_scores_gemma":[0.99891126,0.00043127986,0.00024057449,0.00010956086,0.00008848705,0.00021891443],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00064257806,0.00054508593,0.000373615,0.0013599654,0.0005653891,0.0005558486,0.0005678196,0.00087808387,0.0060797287],"category_scores_gemma":[0.0024512212,0.00030484513,0.00063835894,0.0012049525,0.00032082302,0.0001928539,0.0005057539,0.00082245225,0.0006091723],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.007093378,0.00048175015,0.7480928,0.00018257156,0.0017223583,0.0073327487,0.0006368819,0.0005941464,0.18468909,0.00097133464,0.0049270894,0.043275867],"study_design_scores_gemma":[0.00034623357,0.0005745686,0.97868437,0.000027771252,0.0007067989,0.007235053,0.00017007638,0.0010297672,0.006848355,0.00074724574,0.00360481,0.000024973122],"about_ca_topic_score_codex":0.0026089735,"about_ca_topic_score_gemma":0.0022680536,"teacher_disagreement_score":0.0060797287,"about_ca_system_score_codex":0.00018289477,"about_ca_system_score_gemma":0.00020429777,"threshold_uncertainty_score":0.020338714},"labels":[],"label_agreement":null},{"id":"W1970504500","doi":"10.1038/ng.3253","title":"Germline mutations in ETV6 are associated with thrombocytopenia, red cell macrocytosis and predisposition to lymphoblastic leukemia","year":2015,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Acute Myeloid Leukemia Research","field":"Medicine","cited_by":329,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"SickKids Foundation; University Health Network; Toronto Western Hospital; Hospital for Sick Children; University of Toronto","funders":"National Center for Advancing Translational Sciences; National Institute of General Medical Sciences; National Institutes of Health; National Cancer Institute; National Heart, Lung, and Blood Institute; Canadian Institutes of Health Research","keywords":"Biology; Mutation; Cancer research; Genetics; Leukemia; Germline mutation; Exon; Exome sequencing; Molecular biology; Immunology; Gene","score_opus":0.015936053758994394,"score_gpt":0.28557057557877735,"score_spread":0.269634521819783,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1970504500","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99732333,0.00033727684,0.00048039286,0.00016222401,0.000026517542,0.00000925837,0.0003015745,0.000028821905,0.0013306256],"genre_scores_gemma":[0.99898964,0.000106413594,0.00026643733,0.00003758409,0.000030844447,0.0000019685015,0.00014632121,0.00000927031,0.0004114613],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99963427,0.00009214788,0.000057284935,0.000066747794,0.00008888758,0.00006063561],"domain_scores_gemma":[0.99896574,0.00041867569,0.00032777942,0.00005051833,0.000049293798,0.00018803985],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00021441169,0.0008267022,0.00032831624,0.0014675362,0.00039578116,0.0004780917,0.0005068835,0.0014040064,0.0041499035],"category_scores_gemma":[0.0016270764,0.00025082062,0.00042212787,0.0013291226,0.00039595828,0.00031285017,0.00036762987,0.0006095745,0.0003854855],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0024320092,0.00027937716,0.48449823,0.00015834082,0.00040942893,0.33766058,0.0006787373,0.0018650516,0.14976771,0.001992737,0.0017551377,0.018502725],"study_design_scores_gemma":[0.00018322915,0.00048000133,0.45080927,0.00007001965,0.0002617862,0.52705073,0.00045545466,0.002966132,0.0127057405,0.0015060891,0.0034500589,0.00006153037],"about_ca_topic_score_codex":0.0007240301,"about_ca_topic_score_gemma":0.0006665368,"teacher_disagreement_score":0.0041499035,"about_ca_system_score_codex":0.00017336948,"about_ca_system_score_gemma":0.000128006,"threshold_uncertainty_score":0.013882816},"labels":[],"label_agreement":null},{"id":"W1970565116","doi":"10.1038/ng.2859","title":"Genetic signature of bacterial pathogen adaptation during chronic pulmonary infections","year":2013,"lang":"en","type":"letter","venue":"Nature Genetics","topic":"Burkholderia infections and melioidosis","field":"Medicine","cited_by":6,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"McMaster University; Population Health Research Institute","funders":"","keywords":"Biology; Cystic fibrosis; Adaptation (eye); Genome; Pathogen; Population; Chronic infection; Genetics; Burkholderia; Computational biology; Evolutionary biology; Gene; Bacteria; Immune system","score_opus":0.009058756557766506,"score_gpt":0.22941969950499666,"score_spread":0.22036094294723016,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1970565116","genre_codex":"commentary","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":null,"domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.43365684,0.0038360157,0.0017382401,0.5317296,0.0098462505,0.0000678977,0.00027449106,0.00015610359,0.018694624],"genre_scores_gemma":[0.8507337,0.0013108106,0.0008318664,0.12677719,0.016340207,0.000038600418,0.00007733336,0.000034371562,0.0038559376],"study_design_codex":"case_report","study_design_gemma":"observational","domain_scores_codex":[0.999464,0.00019410267,0.000057642752,0.00006315092,0.000087959605,0.00013313461],"domain_scores_gemma":[0.9983341,0.00093727524,0.0001572314,0.000121631885,0.00017824472,0.00027156403],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0006007728,0.00021357636,0.00039759668,0.00026343515,0.00067756284,0.000691909,0.00043313432,0.005809738,0.001267484],"category_scores_gemma":[0.0038286354,0.000173663,0.00028303073,0.00023379631,0.0009036711,0.0006343319,0.00038369282,0.0039399504,0.00049813115],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0044974727,0.0005455379,0.18909137,0.0002897435,0.00017637265,0.33943254,0.0019389533,0.0010167147,0.075437106,0.01013946,0.28330943,0.094125405],"study_design_scores_gemma":[0.00096008164,0.0017264149,0.35594037,0.00047135036,0.00027745008,0.3672038,0.0037156695,0.008111791,0.0150567135,0.030417534,0.21585526,0.00026352302],"about_ca_topic_score_codex":0.00086061034,"about_ca_topic_score_gemma":0.0013931745,"teacher_disagreement_score":0.005809738,"about_ca_system_score_codex":0.0009740192,"about_ca_system_score_gemma":0.00029706868,"threshold_uncertainty_score":0.0070670247},"labels":[],"label_agreement":null},{"id":"W1971159424","doi":"10.1038/ng0205-110","title":"Assessing the validity of the association between the SUMO4 M55V variant and risk of type 1 diabetes","year":2005,"lang":"en","type":"letter","venue":"Nature Genetics","topic":"Endoplasmic Reticulum Stress and Disease","field":"Biochemistry, Genetics and Molecular Biology","cited_by":74,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"McGill University; Montreal Children's Hospital; McGill University and Génome Québec Innovation Centre; University of Toronto","funders":"","keywords":"Biology; Type 2 diabetes; Association (psychology); Genetics; Genome-wide association study; Diabetes mellitus; Genetic association; Single-nucleotide polymorphism; Gene; Endocrinology; Genotype; Psychology","score_opus":0.009353638518201032,"score_gpt":0.2616002551637763,"score_spread":0.25224661664557524,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1971159424","genre_codex":"commentary","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":null,"domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.29373577,0.0036209556,0.0022138827,0.6687733,0.019706998,0.00007633566,0.00060323277,0.00007343509,0.011196116],"genre_scores_gemma":[0.7705343,0.0016123496,0.0020749676,0.19510256,0.02717095,0.000063947366,0.00024854176,0.00004482795,0.0031477108],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99390644,0.0033292642,0.0008855262,0.00059133914,0.00091499824,0.0003724343],"domain_scores_gemma":[0.942159,0.047905833,0.0012718417,0.0021103588,0.0052300994,0.0013228536],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.008747649,0.00059390196,0.0013963185,0.000752854,0.0013308142,0.0014191436,0.0016348821,0.012240761,0.0025361087],"category_scores_gemma":[0.07431499,0.00033434742,0.00091751013,0.00055276416,0.0017676742,0.001116413,0.00088083284,0.007569321,0.0015873474],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0072237425,0.00062324,0.5279349,0.0004498299,0.0014200029,0.080876336,0.0029014063,0.0012814448,0.010898839,0.0074461894,0.24290927,0.11603484],"study_design_scores_gemma":[0.0037871029,0.0043971506,0.4695502,0.0014150406,0.002154381,0.17136145,0.0061267107,0.028195867,0.016386399,0.07544718,0.2205818,0.0005966638],"about_ca_topic_score_codex":0.0021860546,"about_ca_topic_score_gemma":0.0015322304,"teacher_disagreement_score":0.012240761,"about_ca_system_score_codex":0.0010135908,"about_ca_system_score_gemma":0.00062172726,"threshold_uncertainty_score":0.046262562},"labels":[],"label_agreement":null},{"id":"W1971624220","doi":"10.1038/ng.138","title":"Altered brain microRNA biogenesis contributes to phenotypic deficits in a 22q11-deletion mouse model","year":2008,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Congenital heart defects research","field":"Biochemistry, Genetics and Molecular Biology","cited_by":655,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of British Columbia","funders":"National Institute of Mental Health; National Institutes of Health","keywords":"Haploinsufficiency; Biology; microRNA; Genetics; Phenotype; Biogenesis; Locus (genetics); Gene; Synteny; Chromosome","score_opus":0.014757661901427003,"score_gpt":0.28178345433936214,"score_spread":0.2670257924379351,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1971624220","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.98334724,0.0010985142,0.008597335,0.0009719992,0.00023329305,0.00013522558,0.0020550326,0.00074187055,0.0028195162],"genre_scores_gemma":[0.9714291,0.002209947,0.010057123,0.0003105242,0.000107904896,0.0004162793,0.0015261546,0.0006189435,0.013323943],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99931777,0.000108867054,0.000098442055,0.00021370416,0.00018360466,0.00007771961],"domain_scores_gemma":[0.99906915,0.00020403584,0.00036030082,0.00008809423,0.000050151233,0.00022827406],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0005358758,0.0030422125,0.00083074183,0.0030861453,0.00083685905,0.00082439336,0.0014410102,0.0016803873,0.00690947],"category_scores_gemma":[0.0005469066,0.0008260282,0.0006693938,0.0006922306,0.0021799006,0.00071474595,0.0011559696,0.002433251,0.0012908907],"study_design_candidate":"bench_or_experimental","study_design_consensus":"bench_or_experimental","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0005586502,0.00016672019,0.00045958217,0.000071683986,0.00003896581,0.0025353457,0.000062805244,0.00031081733,0.9926783,0.0008403389,0.0003227889,0.0019540682],"study_design_scores_gemma":[0.0003764718,0.0006952425,0.012576316,0.00006847664,0.00035862517,0.010976328,0.00024730744,0.003471452,0.9637858,0.0012374108,0.0061263023,0.000080227124],"about_ca_topic_score_codex":0.001283072,"about_ca_topic_score_gemma":0.001983737,"teacher_disagreement_score":0.00690947,"about_ca_system_score_codex":0.0005347122,"about_ca_system_score_gemma":0.0006413996,"threshold_uncertainty_score":0.023114443},"labels":[],"label_agreement":null},{"id":"W1972240813","doi":"10.1038/ng.3284","title":"Germline RECQL mutations are associated with breast cancer susceptibility","year":2015,"lang":"en","type":"article","venue":"Nature Genetics","topic":"BRCA gene mutations in cancer","field":"Biochemistry, Genetics and Molecular Biology","cited_by":189,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Women's College Hospital; University of Toronto; McGill University Health Centre; Centre hospitalier universitaire de Québec; McGill University; Jewish General Hospital; McGill University and Génome Québec Innovation Centre","funders":"Canadian Institutes of Health Research","keywords":"Breast cancer; Biology; Gene; Exome sequencing; Genetics; Cancer; Germline; Exome; Germline mutation; Population; Mutation; DNA sequencing; Oncology; Internal medicine; Medicine","score_opus":0.014182445109025303,"score_gpt":0.2942865319465853,"score_spread":0.28010408683756,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1972240813","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99527377,0.0016214951,0.0004343902,0.00031197257,0.00003163816,0.0000056474614,0.000333246,0.000057290235,0.0019305386],"genre_scores_gemma":[0.99881136,0.00027006352,0.00022860181,0.00003591433,0.0000300348,0.000002006358,0.00010278638,0.000010864364,0.0005084533],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99963224,0.00008971683,0.00003790161,0.00008694965,0.000101759964,0.000051424664],"domain_scores_gemma":[0.9984584,0.0004625111,0.00070057594,0.00009785806,0.00011425086,0.00016635931],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00028161786,0.00043115858,0.00033212805,0.0017710456,0.0002767462,0.00053707336,0.0004754646,0.00086856104,0.0039768927],"category_scores_gemma":[0.0023180444,0.00029516415,0.00031433065,0.0012825136,0.00034628776,0.00023487995,0.0002724633,0.000513505,0.00043980876],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0017099453,0.00013940276,0.8907852,0.00009687785,0.0003481775,0.014032565,0.00023606843,0.00051263877,0.074854486,0.0006172863,0.00084764505,0.015819816],"study_design_scores_gemma":[0.000048792437,0.00016879458,0.9497939,0.000027786567,0.00022421888,0.03671313,0.0001875428,0.00087375514,0.009350186,0.0006187517,0.0019669102,0.000026323605],"about_ca_topic_score_codex":0.0012388522,"about_ca_topic_score_gemma":0.000787765,"teacher_disagreement_score":0.0039768927,"about_ca_system_score_codex":0.00018888441,"about_ca_system_score_gemma":0.00014044488,"threshold_uncertainty_score":0.013303995},"labels":[],"label_agreement":null},{"id":"W1973173778","doi":"10.1038/ng.904","title":"The autoimmune disease–associated PTPN22 variant promotes calpain-mediated Lyp/Pep degradation associated with lymphocyte and dendritic cell hyperresponsiveness","year":2011,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Protein Tyrosine Phosphatases","field":"Biochemistry, Genetics and Molecular Biology","cited_by":250,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"McGill University; Royal Victoria Regional Health Centre; Canadian Institutes of Health Research; Princess Margaret Cancer Centre; Royal Victoria Hospital; University of Toronto; Toronto General Hospital; Lunenfeld-Tanenbaum Research Institute; Mount Sinai Hospital; Ontario Institute for Cancer Research","funders":"Canadian Institutes of Health Research","keywords":"PTPN22; Calpain; Biology; Molecular biology; Immunology; Autoimmune disease; Autoimmunity; Antibody; Gene; Biochemistry; Genotype; Enzyme","score_opus":0.007090732544122032,"score_gpt":0.2063910014012272,"score_spread":0.19930026885710517,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1973173778","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99851733,0.00029782933,0.0004988583,0.000083106985,0.000026632239,0.000007414078,0.00009945873,0.000023248444,0.0004461871],"genre_scores_gemma":[0.9991085,0.00008355126,0.00018681436,0.000034581313,0.00001612825,0.0000048139104,0.00010286276,0.000011261716,0.00045146453],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99979204,0.00004683991,0.000026727343,0.000045783978,0.00003821657,0.000050441016],"domain_scores_gemma":[0.9997181,0.00006043592,0.00008021331,0.000033994616,0.000019518917,0.00008765267],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00019804611,0.00048201994,0.00026685873,0.00030143603,0.00018088179,0.00033488625,0.00021501152,0.00050720054,0.0024824988],"category_scores_gemma":[0.00039539233,0.00015899951,0.00031451322,0.00014075982,0.00031618087,0.00018093266,0.00032800244,0.00079311855,0.0004278296],"study_design_candidate":"bench_or_experimental","study_design_consensus":"bench_or_experimental","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00054586,0.000057438432,0.0026730392,0.000020750513,0.000020058491,0.0035925945,0.000021787058,0.00006466494,0.9916943,0.00015270723,0.00013781367,0.0010190071],"study_design_scores_gemma":[0.0003641341,0.0015788267,0.18279743,0.000022838283,0.00016926849,0.08208274,0.00021373821,0.0049372204,0.72240794,0.0007786963,0.0046073818,0.00003978337],"about_ca_topic_score_codex":0.00035318933,"about_ca_topic_score_gemma":0.00039735663,"teacher_disagreement_score":0.0024824988,"about_ca_system_score_codex":0.00021535231,"about_ca_system_score_gemma":0.00010258764,"threshold_uncertainty_score":0.008304775},"labels":[],"label_agreement":null},{"id":"W1974108104","doi":"10.1038/ng1005-1016","title":"Re-examination of P-PTEN staining patterns in the intestinal crypt","year":2005,"lang":"en","type":"letter","venue":"Nature Genetics","topic":"PI3K/AKT/mTOR signaling in cancer","field":"Biochemistry, Genetics and Molecular Biology","cited_by":18,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Toronto","funders":"","keywords":"Biology; Crypt; PTEN; Staining; Molecular biology; Genetics; Apoptosis; Endocrinology","score_opus":0.012874190281880067,"score_gpt":0.2791076121711341,"score_spread":0.26623342188925403,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1974108104","genre_codex":"empirical","genre_gemma":"other","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"other","genre_consensus":null,"domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.5661086,0.019188654,0.042776026,0.27858722,0.02558896,0.0003131955,0.0016167584,0.0026743317,0.063146204],"genre_scores_gemma":[0.8992293,0.0064597647,0.0144919995,0.033522937,0.009038137,0.00012710101,0.00044299063,0.00024602193,0.03644163],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9998349,0.00002644338,0.000019971727,0.000037212987,0.00004024896,0.000041089916],"domain_scores_gemma":[0.99956137,0.00015650081,0.000041722542,0.0000878245,0.00007689598,0.00007575842],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00030417915,0.0002951428,0.00028250288,0.00062976725,0.00031717325,0.0004912482,0.00051318307,0.0021307382,0.0025181428],"category_scores_gemma":[0.00090190634,0.00021439063,0.00036921038,0.00024332285,0.00061183516,0.00046196702,0.00030599735,0.0022233678,0.001124878],"study_design_candidate":"bench_or_experimental","study_design_consensus":"bench_or_experimental","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0026728287,0.00020455378,0.011945129,0.0006764908,0.0001499675,0.21343534,0.00028047894,0.0008454123,0.5620281,0.0071851476,0.08369259,0.116883956],"study_design_scores_gemma":[0.0007025867,0.0007119432,0.06990458,0.00014075614,0.000316963,0.43252933,0.0005951581,0.0075235683,0.25627148,0.008246875,0.2229372,0.00011964881],"about_ca_topic_score_codex":0.00083691487,"about_ca_topic_score_gemma":0.0011072077,"teacher_disagreement_score":0.0025181428,"about_ca_system_score_codex":0.00046966746,"about_ca_system_score_gemma":0.00013326692,"threshold_uncertainty_score":0.008424044},"labels":[],"label_agreement":null},{"id":"W1974720903","doi":"10.1038/ng.2771","title":"The long noncoding RNA SChLAP1 promotes aggressive prostate cancer and antagonizes the SWI/SNF complex","year":2013,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Cancer-related molecular mechanisms research","field":"Biochemistry, Genetics and Molecular Biology","cited_by":683,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Genome British Columbia","funders":"National Cancer Institute; Howard Hughes Medical Institute","keywords":"Biology; Prostate cancer; Long non-coding RNA; SWI/SNF; Chromatin; Metastasis; Cancer research; Prostate; SMARCA4; Locus (genetics); Cancer; Genetics; RNA; Gene; Chromatin remodeling","score_opus":0.009404841671547901,"score_gpt":0.29005568839131146,"score_spread":0.28065084671976354,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1974720903","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9926576,0.001513217,0.0015326524,0.00046210538,0.000054620974,0.0000099440595,0.00025253664,0.00025204773,0.003265137],"genre_scores_gemma":[0.9963421,0.0003041833,0.00045040023,0.00008214105,0.000009627758,0.0000059271306,0.00020296997,0.00003873199,0.0025638572],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.999846,0.000016496597,0.000005125289,0.000029480812,0.000057283298,0.000045548088],"domain_scores_gemma":[0.99981934,0.000023586024,0.00005119313,0.000018133716,0.000011916768,0.00007584622],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00013104279,0.00031570074,0.00016315388,0.00042348795,0.000247951,0.0004384383,0.00024214094,0.0003093672,0.002480204],"category_scores_gemma":[0.00015366873,0.00024995263,0.000168587,0.00014497999,0.00047888167,0.00022962995,0.000424269,0.0009462635,0.00066870137],"study_design_candidate":"bench_or_experimental","study_design_consensus":"bench_or_experimental","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00017355346,0.00002893418,0.002335398,0.00003337846,0.000014373514,0.00025904138,0.000013796217,0.00022914867,0.9922788,0.00062830135,0.00037304216,0.003632274],"study_design_scores_gemma":[0.00004197768,0.00028891023,0.042018082,0.000008857547,0.000032997366,0.0014707192,0.00009239975,0.0032026186,0.9460774,0.0006034139,0.006147272,0.000015349078],"about_ca_topic_score_codex":0.0006806137,"about_ca_topic_score_gemma":0.0023137862,"teacher_disagreement_score":0.002480204,"about_ca_system_score_codex":0.00047605849,"about_ca_system_score_gemma":0.00036015527,"threshold_uncertainty_score":0.008297145},"labels":[],"label_agreement":null},{"id":"W1974754172","doi":"10.1038/ng1644","title":"Disruption of Bardet-Biedl syndrome ciliary proteins perturbs planar cell polarity in vertebrates","year":2005,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Genetic and Kidney Cyst Diseases","field":"Biochemistry, Genetics and Molecular Biology","cited_by":552,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Simon Fraser University","funders":"Wellcome Trust","keywords":"Convergent extension; Biology; Zebrafish; Cell polarity; Cilium; Cell biology; Frizzled; Phenotype; Genetics; Wnt signaling pathway; Neurulation; Axoneme; Gastrulation; Mutant; Gene; Genetic screen; Bardet–Biedl syndrome; Cell; Flagellum; Embryonic stem cell","score_opus":0.00402847792014175,"score_gpt":0.22512703810271764,"score_spread":0.2210985601825759,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1974754172","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99153066,0.0010087115,0.0043869033,0.00042204172,0.000077296056,0.000019910216,0.00038183565,0.0002154713,0.0019572042],"genre_scores_gemma":[0.99566156,0.00034778583,0.00201984,0.00009035373,0.000008645585,0.000012094742,0.00014801028,0.000055565924,0.0016561717],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9996722,0.0000548555,0.000042397493,0.0000588099,0.00012416263,0.000047616126],"domain_scores_gemma":[0.9996691,0.000061403545,0.00012897563,0.000029599963,0.000022524351,0.00008846361],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00020188482,0.00048396323,0.00025691016,0.00097103434,0.00050525065,0.0005448394,0.0003989411,0.00087761163,0.0014931706],"category_scores_gemma":[0.0003219831,0.00044028615,0.000218484,0.00030293124,0.0008944823,0.0002845866,0.0005350918,0.0008302567,0.00068080577],"study_design_candidate":"bench_or_experimental","study_design_consensus":"bench_or_experimental","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.000053781365,0.000008852679,0.00030356337,0.000019495139,0.000008275041,0.00027353957,0.000014579185,0.00021426858,0.9978738,0.00045936866,0.000076922544,0.00069359783],"study_design_scores_gemma":[0.000056749683,0.00009080083,0.011480272,0.000014325734,0.000048776586,0.0022255713,0.000089313675,0.0047591347,0.9770371,0.00034009828,0.0038364027,0.000021444954],"about_ca_topic_score_codex":0.0031090763,"about_ca_topic_score_gemma":0.006570344,"teacher_disagreement_score":0.0031090763,"about_ca_system_score_codex":0.0009482774,"about_ca_system_score_gemma":0.0004765461,"threshold_uncertainty_score":0.0068802834},"labels":[],"label_agreement":null},{"id":"W1975524623","doi":"10.1038/ng0507-571","title":"Reactive oxygen species and the segregation of mtDNA sequence variants","year":2007,"lang":"en","type":"letter","venue":"Nature Genetics","topic":"Mitochondrial Function and Pathology","field":"Biochemistry, Genetics and Molecular Biology","cited_by":8,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"McGill University; Montreal Neurological Institute and Hospital","funders":"","keywords":"Biology; Mitochondrial DNA; Sequence (biology); Genetics; Evolutionary biology; Reactive oxygen species; Computational biology; Gene","score_opus":0.014766900006237468,"score_gpt":0.2575163001603233,"score_spread":0.2427494001540858,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1975524623","genre_codex":"commentary","genre_gemma":"commentary","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"commentary","genre_consensus":"commentary","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.04848444,0.012607134,0.003223384,0.882291,0.03830765,0.00007460847,0.00029478237,0.00026112987,0.014455826],"genre_scores_gemma":[0.3971532,0.011836617,0.0027627284,0.4198276,0.14038268,0.00017250676,0.00033115243,0.0001285829,0.027404971],"study_design_codex":"not_applicable","study_design_gemma":"not_applicable","domain_scores_codex":[0.9992574,0.00033628196,0.000067453526,0.00011469199,0.00015236127,0.00007179644],"domain_scores_gemma":[0.99710494,0.002107195,0.00018435763,0.00016889688,0.00018672961,0.00024781664],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0011727884,0.0006427009,0.0009894078,0.0004990753,0.00076592155,0.0010408345,0.000893618,0.013077584,0.003187087],"category_scores_gemma":[0.006061373,0.0003121664,0.00048034187,0.00029478566,0.0015095918,0.0010377384,0.00048982236,0.008159146,0.0013443097],"study_design_candidate":"not_applicable","study_design_consensus":"not_applicable","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0069543812,0.0004821463,0.014848872,0.0004066919,0.00034921567,0.108329445,0.0005802521,0.00080800697,0.02735548,0.03907141,0.6981015,0.1027126],"study_design_scores_gemma":[0.0028332996,0.0015350702,0.036512196,0.0003983528,0.00052027294,0.13536333,0.0007817182,0.009124559,0.029520733,0.13103378,0.6520731,0.0003036106],"about_ca_topic_score_codex":0.00048635041,"about_ca_topic_score_gemma":0.00076373573,"teacher_disagreement_score":0.013077584,"about_ca_system_score_codex":0.0010015176,"about_ca_system_score_gemma":0.00034695063,"threshold_uncertainty_score":0.0106619},"labels":[],"label_agreement":null},{"id":"W1975940953","doi":"10.1038/ng.2829","title":"Gain-of-function mutations in the phosphatidylserine synthase 1 (PTDSS1) gene cause Lenz-Majewski syndrome","year":2013,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Erythrocyte Function and Pathophysiology","field":"Medicine","cited_by":108,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Alberta","funders":"National Heart, Lung, and Blood Institute; Medical Research Council; National Institute for Health and Care Research; Wellcome Trust","keywords":"Phosphatidylserine; Missense mutation; Biology; Genetics; Cutis laxa; Mutation; Loss function; Gene; Cell biology; Phenotype","score_opus":0.015772265788993347,"score_gpt":0.27145776423377516,"score_spread":0.25568549844478183,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1975940953","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99431026,0.0006267803,0.0017706098,0.000689252,0.00006921954,0.000026533764,0.00026798664,0.00014770328,0.0020915444],"genre_scores_gemma":[0.9983346,0.000195722,0.00080012437,0.000065709195,0.000032487234,0.0000055273485,0.00007735054,0.0000183775,0.00047008097],"study_design_codex":"case_report","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99983096,0.000027921413,0.000024023117,0.000034237837,0.000059050977,0.000023765326],"domain_scores_gemma":[0.999602,0.00015449393,0.00011274777,0.000016125725,0.000018915916,0.00009565952],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00014204884,0.0014381867,0.00037917556,0.001142209,0.00042257996,0.00043890913,0.00052059593,0.0014545642,0.0014858999],"category_scores_gemma":[0.0010846778,0.00031640462,0.0003822429,0.00059571274,0.0007963891,0.00034234094,0.00063563697,0.0009637493,0.00048038698],"study_design_candidate":"bench_or_experimental","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0015177588,0.00020318372,0.04638625,0.00027104095,0.00022259157,0.6208076,0.0006145379,0.002174514,0.30322483,0.0038463273,0.0022550384,0.01847622],"study_design_scores_gemma":[0.0004352678,0.00044864416,0.104910545,0.00007061237,0.00042968508,0.787675,0.00042070245,0.006810819,0.08933715,0.0034878142,0.0058787526,0.000095051146],"about_ca_topic_score_codex":0.00067455653,"about_ca_topic_score_gemma":0.00074785796,"teacher_disagreement_score":0.0014858999,"about_ca_system_score_codex":0.00042489433,"about_ca_system_score_gemma":0.0003205185,"threshold_uncertainty_score":0.0049708486},"labels":[],"label_agreement":null},{"id":"W1977142594","doi":"10.1038/ng.359","title":"Mutations in mitochondrial carrier family gene SLC25A38 cause nonsyndromic autosomal recessive congenital sideroblastic anemia","year":2009,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Porphyrin Metabolism and Disorders","field":"Biochemistry, Genetics and Molecular Biology","cited_by":247,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Centre Hospitalier Universitaire Sainte-Justine; Université de Montréal; Izaak Walton Killam Health Centre; Dalhousie University","funders":"National Institute of Diabetes and Digestive and Kidney Diseases","keywords":"Sideroblastic anemia; Biology; Genetics; Positional cloning; Mutation; Gene; Mitochondrial DNA; Mitochondrion; Phenotype","score_opus":0.0056448725650317284,"score_gpt":0.24885092426096805,"score_spread":0.24320605169593632,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1977142594","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9965766,0.0003998661,0.0006369372,0.00015280159,0.00006782548,0.00002143676,0.0004084872,0.000086279564,0.0016496546],"genre_scores_gemma":[0.99761826,0.00014214945,0.00071810145,0.000044013843,0.00004314081,0.000011270515,0.0001765369,0.00003133862,0.0012150306],"study_design_codex":"case_report","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99979144,0.000027812861,0.000031768555,0.00004762662,0.00007245341,0.00002883262],"domain_scores_gemma":[0.9994574,0.00017090293,0.00016378291,0.00003609862,0.000034837456,0.00013697488],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00017250492,0.0014596866,0.00047854855,0.0008223966,0.0006384529,0.00023110001,0.0007349618,0.0011709221,0.003941305],"category_scores_gemma":[0.0008220138,0.00032397345,0.00036301377,0.0005846783,0.0007146039,0.00026321976,0.0004845527,0.000387543,0.0006983841],"study_design_candidate":"bench_or_experimental","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0008784678,0.00016416752,0.038203813,0.0002249927,0.00019845732,0.7091321,0.00080332346,0.0007932746,0.2364207,0.0014320483,0.0022553303,0.009493362],"study_design_scores_gemma":[0.00034069992,0.0008831885,0.20270559,0.00008704737,0.00060025067,0.71215326,0.0007097215,0.005364,0.06402816,0.0017163545,0.011302268,0.00010946608],"about_ca_topic_score_codex":0.0021279885,"about_ca_topic_score_gemma":0.0034233741,"teacher_disagreement_score":0.003941305,"about_ca_system_score_codex":0.0004373463,"about_ca_system_score_gemma":0.00024648933,"threshold_uncertainty_score":0.013184965},"labels":[],"label_agreement":null},{"id":"W1977170771","doi":"10.1038/ng.2370","title":"Exome sequencing identifies NMNAT1 mutations as a cause of Leber congenital amaurosis","year":2012,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Retinal Development and Disorders","field":"Biochemistry, Genetics and Molecular Biology","cited_by":142,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"SickKids Foundation; Hospital for Sick Children","funders":"","keywords":"Biology; Genetics; Missense mutation; Exome sequencing; Retinal degeneration; Nonsense mutation; Mutation; Compound heterozygosity; Retinitis pigmentosa; Exome; Gene","score_opus":0.011751519529321955,"score_gpt":0.2727102976817879,"score_spread":0.26095877815246593,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1977170771","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9945373,0.0003929033,0.0010580398,0.00068230217,0.00007657912,0.000015742797,0.0005006422,0.00009440238,0.0026420415],"genre_scores_gemma":[0.9982375,0.0001170676,0.0007450114,0.00010631097,0.00003872866,0.0000045305455,0.00013705084,0.000018995543,0.0005948637],"study_design_codex":"case_report","study_design_gemma":"observational","domain_scores_codex":[0.9996904,0.000026850315,0.00004210565,0.000093065384,0.00009284837,0.000054765496],"domain_scores_gemma":[0.99927455,0.00037327068,0.00012179082,0.000029855744,0.000058631755,0.00014197541],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00025061722,0.0011518745,0.00040607885,0.001498035,0.00075684563,0.000649862,0.0005534376,0.002140248,0.0026358212],"category_scores_gemma":[0.0015069885,0.0002671772,0.000409273,0.00056849245,0.00054982206,0.00041912816,0.00057018665,0.00066422066,0.00049590354],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0007121391,0.00009744231,0.049361676,0.000113928676,0.000073361996,0.7356393,0.00060169346,0.0010881326,0.1973095,0.0013748078,0.0016646085,0.011963501],"study_design_scores_gemma":[0.00008226577,0.00024964396,0.14921403,0.00007186202,0.00021087247,0.7684676,0.00040641555,0.0064598797,0.0689273,0.0018830849,0.003956309,0.000070667724],"about_ca_topic_score_codex":0.0016094054,"about_ca_topic_score_gemma":0.001911138,"teacher_disagreement_score":0.0026358212,"about_ca_system_score_codex":0.00053750636,"about_ca_system_score_gemma":0.0002602053,"threshold_uncertainty_score":0.008817673},"labels":[],"label_agreement":null},{"id":"W1977789763","doi":"10.1038/ng957","title":"Mutant frizzled-4 disrupts retinal angiogenesis in familial exudative vitreoretinopathy","year":2002,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Wnt/β-catenin signaling in development and cancer","field":"Biochemistry, Genetics and Molecular Biology","cited_by":476,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of British Columbia; Western University; Xenon Pharmaceuticals (Canada); Izaak Walton Killam Health Centre; Dalhousie University","funders":"","keywords":"Frizzled; Biology; Wnt signaling pathway; Genetics; Positional cloning; Mutant; Wild type; Cell biology; Signal transduction; Gene","score_opus":0.00828874880210074,"score_gpt":0.23838975799345635,"score_spread":0.23010100919135562,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1977789763","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99431014,0.00089115556,0.0026016883,0.00024011698,0.00008131699,0.000029357176,0.00023691544,0.00017889269,0.0014304032],"genre_scores_gemma":[0.9961189,0.0002902258,0.0014861097,0.00005527405,0.000015394788,0.000018663899,0.00006999807,0.00005869858,0.0018868196],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.999567,0.00013084414,0.000055753135,0.00007268009,0.0001121967,0.00006151156],"domain_scores_gemma":[0.99942255,0.00018952938,0.00019091298,0.000036383775,0.000025965117,0.00013474733],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0003239389,0.00078637304,0.00048851327,0.0011469852,0.0005979714,0.0004370883,0.000731133,0.0010191184,0.002540932],"category_scores_gemma":[0.00060314004,0.00044749584,0.0005089047,0.00034991698,0.0009310902,0.00024108586,0.0005474271,0.0009637723,0.00032646098],"study_design_candidate":"bench_or_experimental","study_design_consensus":"bench_or_experimental","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00057007186,0.00011967375,0.0005272155,0.000049859333,0.000058990117,0.0033749,0.000063191386,0.00055076706,0.9917965,0.0009924344,0.00018040615,0.0017158953],"study_design_scores_gemma":[0.0005274845,0.00060106686,0.014444114,0.000037454603,0.0002813353,0.014330937,0.00020856182,0.0114550935,0.9519998,0.00084283756,0.005215406,0.000055911234],"about_ca_topic_score_codex":0.00630199,"about_ca_topic_score_gemma":0.0067324946,"teacher_disagreement_score":0.00630199,"about_ca_system_score_codex":0.0011130425,"about_ca_system_score_gemma":0.0004578605,"threshold_uncertainty_score":0.012530625},"labels":[],"label_agreement":null},{"id":"W1978942485","doi":"10.1038/ng2059","title":"Genetic variation in Mon1a affects protein trafficking and modifies macrophage iron loading in mice","year":2007,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Iron Metabolism and Disorders","field":"Medicine","cited_by":70,"is_retracted":false,"has_abstract":false,"route_ca_aff":false,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"","funders":"National Institutes of Health; National Institute of Diabetes and Digestive and Kidney Diseases; Genome Canada","keywords":"Biology; Quantitative trait locus; Congenic; Allele; Locus (genetics); Gene; Genetics; Transferrin; Macrophage; Cell biology; Biochemistry","score_opus":0.005838986547880901,"score_gpt":0.24878757772226717,"score_spread":0.24294859117438627,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1978942485","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9917086,0.00046338208,0.0042519555,0.0004699724,0.00012618797,0.000045254186,0.0014465998,0.0003828483,0.0011052771],"genre_scores_gemma":[0.98897386,0.0004179702,0.0045536696,0.00031094265,0.000052256044,0.00009003333,0.00061968475,0.00058039656,0.0044012335],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99908566,0.00019408084,0.000119421704,0.00028068773,0.00014537493,0.00017470651],"domain_scores_gemma":[0.99840957,0.00030814146,0.00075783173,0.00010919737,0.000051341096,0.00036400685],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0005487692,0.0015454192,0.00073542667,0.0021164615,0.00066183176,0.00071522704,0.0012029564,0.0019919379,0.0056553264],"category_scores_gemma":[0.0006061774,0.0007574041,0.0010808464,0.0006550467,0.0015735773,0.00029833082,0.000927529,0.0018058796,0.00079330266],"study_design_candidate":"bench_or_experimental","study_design_consensus":"bench_or_experimental","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0011660629,0.00009946839,0.0004449049,0.000042357035,0.000057354173,0.00039938663,0.000043419313,0.00023158456,0.99599314,0.00043369093,0.00010536329,0.0009833145],"study_design_scores_gemma":[0.0008710611,0.0011966479,0.03452366,0.00012207653,0.000675026,0.0041224966,0.00031791534,0.007132719,0.9428362,0.0012105361,0.0068366528,0.0001549919],"about_ca_topic_score_codex":0.0028325,"about_ca_topic_score_gemma":0.0044978866,"teacher_disagreement_score":0.0056553264,"about_ca_system_score_codex":0.001174947,"about_ca_system_score_gemma":0.0005598753,"threshold_uncertainty_score":0.018918931},"labels":[],"label_agreement":null},{"id":"W1979689648","doi":"10.1038/ng.2007.47","title":"Polymorphism at the TNF superfamily gene TNFSF4 confers susceptibility to systemic lupus erythematosus","year":2007,"lang":"en","type":"article","venue":"Nature Genetics","topic":"T-cell and B-cell Immunology","field":"Immunology and Microbiology","cited_by":219,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Université de Montréal; Montreal Heart Institute","funders":"National Institute of Diabetes and Digestive and Kidney Diseases; National Institute of Allergy and Infectious Diseases; National Center for Research Resources; Broad Institute; Wellcome Trust","keywords":"Biology; Immunology; Tumor necrosis factor alpha; SUPERFAMILY; Gene; Genetics","score_opus":0.009538514680234323,"score_gpt":0.23243945108856312,"score_spread":0.2229009364083288,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1979689648","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9989103,0.00006893738,0.00036592106,0.000082395585,0.000016711654,0.0000034507634,0.00006941522,0.000017824239,0.00046505893],"genre_scores_gemma":[0.999032,0.000032816104,0.00028501867,0.000022160506,0.000029016532,0.0000025607867,0.000071106755,0.000008510862,0.0005166956],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.99959475,0.0001734761,0.000036143956,0.00006313443,0.000056360874,0.000076146236],"domain_scores_gemma":[0.9990798,0.00039832844,0.0001932064,0.000077000535,0.000057816447,0.00019393115],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0003934246,0.0005501652,0.00037607533,0.0009805831,0.00045555533,0.00029898115,0.0002524215,0.0006895705,0.0047235494],"category_scores_gemma":[0.0008358091,0.00024405963,0.0004711991,0.00050829747,0.00042936316,0.00013538878,0.00025606964,0.0006688334,0.00041466203],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.011418666,0.0007196594,0.3615398,0.00009135143,0.0005973022,0.008062205,0.00035586028,0.0009608429,0.60263073,0.0009763966,0.0006287519,0.012018489],"study_design_scores_gemma":[0.0007184829,0.0025992969,0.91177243,0.000071430404,0.00085850124,0.02789551,0.0005246607,0.004772138,0.046328727,0.001910537,0.002477699,0.00007063216],"about_ca_topic_score_codex":0.001262288,"about_ca_topic_score_gemma":0.00064373383,"teacher_disagreement_score":0.0047235494,"about_ca_system_score_codex":0.0002563288,"about_ca_system_score_gemma":0.0002011192,"threshold_uncertainty_score":0.015801847},"labels":[],"label_agreement":null},{"id":"W1980516963","doi":"10.1038/ng.473","title":"Global patterns of cis variation in human cells revealed by high-density allelic expression analysis","year":2009,"lang":"en","type":"article","venue":"Nature Genetics","topic":"RNA Research and Splicing","field":"Biochemistry, Genetics and Molecular Biology","cited_by":219,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"McGill University; Centre Hospitalier Universitaire Sainte-Justine; Université de Montréal; McGill University Health Centre; McGill University and Génome Québec Innovation Centre","funders":"National Center for Research Resources","keywords":"Biology; International HapMap Project; Genetics; Single-nucleotide polymorphism; RefSeq; Allele; Gene; Genetic variation; Copy-number variation; Genome; Computational biology; Genotype","score_opus":0.004218139956606074,"score_gpt":0.27024168313749586,"score_spread":0.2660235431808898,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1980516963","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99203616,0.0007557866,0.0056743575,0.000051178205,0.000005593279,0.000007914553,0.0003861942,0.000048179325,0.0010346475],"genre_scores_gemma":[0.9960567,0.00030767868,0.0023820798,0.00003061492,0.000005338209,0.00001039437,0.0004999322,0.00002242584,0.00068491953],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.999826,0.000028435988,0.000015602349,0.000054309894,0.000047029134,0.000028612263],"domain_scores_gemma":[0.9997665,0.000094348914,0.000029279963,0.00004334154,0.000041260068,0.000025264218],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00017900235,0.00009483845,0.00021310098,0.00048018646,0.00021263154,0.00059948786,0.00020272641,0.00015858994,0.0007937976],"category_scores_gemma":[0.0003139129,0.00017870204,0.00014308552,0.0004564514,0.00023574416,0.00013047448,0.0002722732,0.0003739783,0.00035843768],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.000146505,0.000009948174,0.004862947,0.000013602652,0.000017505972,0.00006337714,0.000071288436,0.00011609334,0.991488,0.00025798174,0.0000377658,0.0029150383],"study_design_scores_gemma":[0.000031154508,0.00020844294,0.2504057,0.000007117718,0.00013931624,0.0019236406,0.0004014361,0.0043184324,0.7378934,0.0008116753,0.0038287076,0.000031015355],"about_ca_topic_score_codex":0.0014878602,"about_ca_topic_score_gemma":0.002577353,"teacher_disagreement_score":0.0014878602,"about_ca_system_score_codex":0.0001352462,"about_ca_system_score_gemma":0.000096738666,"threshold_uncertainty_score":0.0029583573},"labels":[],"label_agreement":null},{"id":"W1980587393","doi":"10.1038/ng1308","title":"A conserved developmental program for sensory organ formation in Drosophila melanogaster","year":2004,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Developmental Biology and Gene Regulation","field":"Biochemistry, Genetics and Molecular Biology","cited_by":84,"is_retracted":false,"has_abstract":false,"route_ca_aff":false,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"","funders":"Institute of Genetics; Japan Society for the Promotion of Science","keywords":"Biology; Decapentaplegic; Drosophila melanogaster; PAX6; Imaginal disc; Hox gene; Eye development; Compound eye; Sensory system; Ectopic expression; Genetics; Antennapedia; Fate mapping; Melanogaster; Cell biology; Neuroscience; Gene; Homeobox; Transcription factor; Embryonic stem cell","score_opus":0.009040106262076452,"score_gpt":0.2590879848059954,"score_spread":0.2500478785439189,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1980587393","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9717084,0.002666971,0.015802192,0.00027088472,0.000080082216,0.0000694577,0.00079750805,0.00046389713,0.008140666],"genre_scores_gemma":[0.9847284,0.0006348059,0.005563563,0.00017310625,0.000013176308,0.00004249067,0.00070723024,0.00009538225,0.008041829],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9999198,0.000005862126,0.000005785454,0.000027741988,0.000021771677,0.00001899124],"domain_scores_gemma":[0.99986625,0.0000132714185,0.00003266517,0.000019452562,0.000022206312,0.000046185807],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.000069787,0.00029438877,0.00018914539,0.00033715958,0.0003833356,0.00042781982,0.0002696948,0.0002638006,0.000889112],"category_scores_gemma":[0.00011570367,0.00031322113,0.00028827562,0.00013023893,0.00031718175,0.0002999905,0.00035679576,0.00052097987,0.00040482864],"study_design_candidate":"bench_or_experimental","study_design_consensus":"bench_or_experimental","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.000042648862,0.0000062811937,0.00038785618,0.000024435027,0.0000034706013,0.00016431183,0.000016178961,0.0000915582,0.99618465,0.000819021,0.000115486044,0.0021441444],"study_design_scores_gemma":[0.000028754817,0.00015945743,0.07676389,0.000023783943,0.000025321424,0.0012269575,0.00008893901,0.0018394274,0.910393,0.0007525202,0.008678803,0.000019138055],"about_ca_topic_score_codex":0.0020221707,"about_ca_topic_score_gemma":0.005425639,"teacher_disagreement_score":0.0020221707,"about_ca_system_score_codex":0.0005597717,"about_ca_system_score_gemma":0.0003919616,"threshold_uncertainty_score":0.0040614605},"labels":[],"label_agreement":null},{"id":"W1980725116","doi":"10.1038/ng.764","title":"Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47","year":2011,"lang":"en","type":"review","venue":"Nature Genetics","topic":"Inflammatory Bowel Disease","field":"Biochemistry, Genetics and Molecular Biology","cited_by":1353,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Hospital for Sick Children; Mount Sinai Hospital; SickKids Foundation; University of Toronto; Hôpital Maisonneuve-Rosemont; Université de Montréal; Montreal Heart Institute","funders":"National Institute of Diabetes and Digestive and Kidney Diseases; Else Kröner-Fresenius-Stiftung; Shire; National Heart, Lung, and Blood Institute; Exzellenzclusters Entzündungsforschung; National Institutes of Health; Svenska Läkaresällskapet; Adessium Foundation; Karolinska Institutet; Fonds Wetenschappelijk Onderzoek; Crohn's and Colitis UK; Fonds De La Recherche Scientifique - FNRS; Cedars-Sinai Medical Center; Deutsche Forschungsgemeinschaft; National Center for Research Resources; National Institute of Allergy and Infectious Diseases; National Center for Advancing Translational Sciences; Leona M. and Harry B. Helmsley Charitable Trust; Medical Research Council; Swedish Cancer Foundation; Nederlandse Organisatie voor Wetenschappelijk Onderzoek; ALS Association; Wellcome Trust; National Institute for Health and Care Research; Abbott Laboratories; National Health and Medical Research Council","keywords":"Biology; Ulcerative colitis; Genetics; Meta-analysis; Computational biology; Internal medicine; Disease","score_opus":0.035946806050263104,"score_gpt":0.3296221768317765,"score_spread":0.2936753707815134,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1980725116","genre_codex":"review","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":null,"domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.002066978,0.99589974,0.00055795367,0.0005001873,0.00015969998,0.000008753604,0.00023389037,0.000015941034,0.00055685034],"genre_scores_gemma":[0.021113863,0.9747864,0.0014999757,0.0010948956,0.00037459267,0.000029045717,0.0006624789,0.000011395182,0.00042746507],"study_design_codex":"design_other","study_design_gemma":"meta_analysis","domain_scores_codex":[0.99923444,0.000233524,0.000114234594,0.0002034693,0.00016344183,0.000050919938],"domain_scores_gemma":[0.99771655,0.0018074452,0.00020152387,0.00008840794,0.00013522706,0.000050858933],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.002333911,0.0015286133,0.004039117,0.0014700952,0.0001921128,0.0013080804,0.001124864,0.0014290547,0.0037636377],"category_scores_gemma":[0.0037151265,0.00045007182,0.003365005,0.002449276,0.0003665492,0.0004931187,0.0006099583,0.0011741593,0.00064144883],"study_design_candidate":"meta_analysis","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0030457012,0.00010903835,0.020602418,0.061229702,0.027175868,0.002119836,0.000078377634,0.001581559,0.0040665776,0.0019547727,0.018645946,0.8593902],"study_design_scores_gemma":[0.0032707823,0.0018369777,0.15885265,0.033515815,0.21677986,0.018435404,0.00023431494,0.0015451371,0.006438081,0.010026846,0.5487096,0.0003545677],"about_ca_topic_score_codex":0.0016457683,"about_ca_topic_score_gemma":0.0046454407,"teacher_disagreement_score":0.004039117,"about_ca_system_score_codex":0.0005359361,"about_ca_system_score_gemma":0.0012149053,"threshold_uncertainty_score":0.012590647},"labels":[],"label_agreement":null},{"id":"W1980767402","doi":"10.1038/ng.2950","title":"Recurrent somatic mutations in ACVR1 in pediatric midline high-grade astrocytoma","year":2014,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Glioma Diagnosis and Treatment","field":"Medicine","cited_by":467,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Université de Montréal; Centre Hospitalier Universitaire Sainte-Justine; McGill University; McGill Genome Centre; McGill University Health Centre; Montreal Children's Hospital","funders":"Hungarian Scientific Research Fund; McGill University; Génome Québec; National Cancer Institute; Children's Hospital Foundation; Canadian Institutes of Health Research; Genome Canada; Dana-Farber Cancer Institute","keywords":"Biology; Histone; Epigenetics; Histone H3; Cancer research; Mutation; DNA methylation; Exome sequencing; Germline mutation; Genetics; Gene; Gene expression","score_opus":0.009874758272371812,"score_gpt":0.2801562034248023,"score_spread":0.27028144515243047,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1980767402","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99576867,0.0008934046,0.00078765606,0.00016376117,0.000020486425,0.000011958608,0.00023753758,0.000066521134,0.0020500633],"genre_scores_gemma":[0.9989237,0.00023409637,0.000577193,0.000018529985,0.0000104286055,0.000002496467,0.00007903153,0.000016527798,0.00013790719],"study_design_codex":"case_report","study_design_gemma":"observational","domain_scores_codex":[0.99961877,0.000029524472,0.000043044503,0.00008000556,0.00014652903,0.00008204739],"domain_scores_gemma":[0.9994382,0.0001310107,0.00024024572,0.000032435677,0.000057427715,0.000100711535],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0001708034,0.0004149232,0.00032616142,0.0008777882,0.0004613076,0.0006141315,0.000505692,0.0008012556,0.0013488374],"category_scores_gemma":[0.0011039843,0.00024661442,0.00039424156,0.00089717825,0.0004944017,0.00028448837,0.00036023857,0.00045435491,0.00035624974],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.000567051,0.0000966779,0.3218816,0.00023676026,0.00020347333,0.44357836,0.0009435802,0.0045014187,0.16401228,0.0019043292,0.0021237761,0.0599507],"study_design_scores_gemma":[0.000038983286,0.00021986155,0.22362675,0.00006987449,0.00027811746,0.7253323,0.000746773,0.0037453359,0.040204436,0.00076877815,0.004924053,0.000044722998],"about_ca_topic_score_codex":0.0026368354,"about_ca_topic_score_gemma":0.004085099,"teacher_disagreement_score":0.0026368354,"about_ca_system_score_codex":0.0006961899,"about_ca_system_score_gemma":0.00049194944,"threshold_uncertainty_score":0.0052430034},"labels":[],"label_agreement":null},{"id":"W1981054886","doi":"10.1038/ng.2218","title":"KLHL3 mutations cause familial hyperkalemic hypertension by impairing ion transport in the distal nephron","year":2012,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Ion Transport and Channel Regulation","field":"Biochemistry, Genetics and Molecular Biology","cited_by":337,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Dalhousie University","funders":"Agence Nationale de la Recherche","keywords":"Nephron; Biology; Distal convoluted tubule; Hyperkalemia; Mutation; Genetics; Endocrinology; Internal medicine; Kidney; Gene; Medicine","score_opus":0.008375350318252697,"score_gpt":0.23480465774421155,"score_spread":0.22642930742595885,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1981054886","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99504673,0.0004463793,0.0023353498,0.0004455404,0.00006240325,0.000011973004,0.00026884454,0.00017043602,0.0012124553],"genre_scores_gemma":[0.9987037,0.00007661935,0.00059175433,0.00008757483,0.000022598839,0.000003363778,0.00006465442,0.000027450233,0.00042214213],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.99970883,0.000043423934,0.00004110268,0.000054624365,0.000107737666,0.000044262488],"domain_scores_gemma":[0.9994814,0.0001685326,0.00014781351,0.000024930545,0.000039128827,0.00013826831],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00019930166,0.0010093484,0.00035188918,0.0004904243,0.00038896335,0.00043604834,0.0003983277,0.0011654828,0.0017235834],"category_scores_gemma":[0.0006018735,0.0002528739,0.00040870122,0.00040988365,0.0007314399,0.0002650925,0.00046706793,0.0006987669,0.0003142183],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0017284267,0.00013555234,0.029520154,0.0002016283,0.0003037438,0.08194969,0.0005136427,0.0017249417,0.8700772,0.0020682407,0.0016164443,0.010160467],"study_design_scores_gemma":[0.0009877529,0.00063652114,0.29921252,0.00012406183,0.0009451091,0.26550052,0.00073989655,0.015891455,0.3992968,0.006332024,0.010112588,0.0002208631],"about_ca_topic_score_codex":0.0023701289,"about_ca_topic_score_gemma":0.0028435197,"teacher_disagreement_score":0.0023701289,"about_ca_system_score_codex":0.0004915763,"about_ca_system_score_gemma":0.00033679864,"threshold_uncertainty_score":0.0057659745},"labels":[],"label_agreement":null},{"id":"W1982088425","doi":"10.1038/ng.2734","title":"The integrated landscape of driver genomic alterations in glioblastoma","year":2013,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Cancer Genomics and Diagnostics","field":"Biochemistry, Genetics and Molecular Biology","cited_by":560,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Princess Margaret Cancer Centre; University Health Network; University of Toronto","funders":"National Cancer Institute; National Institute of Neurological Disorders and Stroke; National Institute of Mental Health","keywords":"Biology; Loss of heterozygosity; Glioma; Phenotype; Cancer research; Loss function; Fusion gene; Gene; Mutation; Genetics; Computational biology; Allele","score_opus":0.0028891638605684986,"score_gpt":0.21821980766322868,"score_spread":0.21533064380266018,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1982088425","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99231863,0.002779807,0.0012396678,0.000494198,0.0000106703,0.0000063670745,0.0006491784,0.00007588897,0.002425693],"genre_scores_gemma":[0.99816716,0.0007067791,0.0003331999,0.0000948472,0.000016440887,0.000003444873,0.00024472323,0.000019720732,0.000413647],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.99970895,0.000029412106,0.000017710512,0.00007254194,0.00010971802,0.00006157136],"domain_scores_gemma":[0.9997111,0.00008546985,0.00009717773,0.000026382855,0.000040539002,0.00003938471],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00026038694,0.0001944787,0.00039939754,0.0014278295,0.00020781017,0.000990953,0.00028290015,0.00034716522,0.0021863044],"category_scores_gemma":[0.0008180926,0.00022891905,0.00017718857,0.0011299767,0.0002875962,0.0006211447,0.00055608066,0.0003387764,0.0002839405],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0012478492,0.00011713591,0.35482717,0.00020263693,0.00040372155,0.0025096382,0.00027656168,0.0040592276,0.49862882,0.0059443233,0.0017510285,0.13003196],"study_design_scores_gemma":[0.000029181252,0.00028604572,0.9443518,0.00003758987,0.00040664716,0.005469187,0.00037659876,0.005686293,0.027750896,0.009080259,0.0064964965,0.000029015306],"about_ca_topic_score_codex":0.0010186975,"about_ca_topic_score_gemma":0.0025033834,"teacher_disagreement_score":0.0021863044,"about_ca_system_score_codex":0.00034724566,"about_ca_system_score_gemma":0.00028763706,"threshold_uncertainty_score":0.007313907},"labels":[],"label_agreement":null},{"id":"W1982772105","doi":"10.1038/ng0708-806","title":"ESR1 gene amplification in breast cancer: a common phenomenon?","year":2008,"lang":"en","type":"letter","venue":"Nature Genetics","topic":"RNA and protein synthesis mechanisms","field":"Biochemistry, Genetics and Molecular Biology","cited_by":66,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Centre for Advancing Health Outcomes; Vancouver Coastal Health; Vancouver Coastal Health Research Institute; University of British Columbia; BC Cancer Agency","funders":"National Cancer Institute","keywords":"Biology; Breast cancer; Gene duplication; Genetics; Cancer; Estrogen receptor alpha; Gene; Computational biology; Estrogen receptor","score_opus":0.009519444712237965,"score_gpt":0.24977011004012867,"score_spread":0.2402506653278907,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1982772105","genre_codex":"commentary","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":null,"domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.058069855,0.032890085,0.004262476,0.87272716,0.020157041,0.00004267133,0.00028497394,0.00032909526,0.011236648],"genre_scores_gemma":[0.4469794,0.03225876,0.0030818009,0.33438674,0.17473188,0.00009812565,0.0002143241,0.0001251666,0.008123828],"study_design_codex":"not_applicable","study_design_gemma":"observational","domain_scores_codex":[0.99920326,0.00020156274,0.00011704795,0.00018009049,0.00017769336,0.00012023517],"domain_scores_gemma":[0.99704117,0.0019498963,0.00032670272,0.00020831291,0.00024392389,0.00022992589],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0015324849,0.00040486205,0.001058812,0.00054538425,0.00039831063,0.0011161051,0.0008659925,0.010406296,0.0019116548],"category_scores_gemma":[0.006665044,0.00030813296,0.0004660344,0.0006001696,0.0016984742,0.0015396292,0.0005369352,0.0052233753,0.0012067029],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0036084403,0.00024335459,0.05002286,0.00094609865,0.00032604468,0.13763049,0.0007808988,0.0008915305,0.02643569,0.03139485,0.4957638,0.2519559],"study_design_scores_gemma":[0.0017670508,0.0011454918,0.06274033,0.00054321473,0.0005975504,0.25564885,0.0014285728,0.0053204014,0.017862536,0.07136953,0.5812971,0.00027924668],"about_ca_topic_score_codex":0.00025472988,"about_ca_topic_score_gemma":0.0004182527,"teacher_disagreement_score":0.010406296,"about_ca_system_score_codex":0.00079681986,"about_ca_system_score_gemma":0.0002880045,"threshold_uncertainty_score":0.008104622},"labels":[],"label_agreement":null},{"id":"W1983270011","doi":"10.1038/ng.2247","title":"A genome-wide association meta-analysis identifies new childhood obesity loci","year":2012,"lang":"en","type":"review","venue":"Nature Genetics","topic":"Genetic Associations and Epidemiology","field":"Biochemistry, Genetics and Molecular Biology","cited_by":438,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Lunenfeld-Tanenbaum Research Institute; Ontario Institute for Cancer Research; McMaster University","funders":"Eunice Kennedy Shriver National Institute of Child Health and Human Development; National Institute of Mental Health; National Institute of Diabetes and Digestive and Kidney Diseases; National Heart, Lung, and Blood Institute; ZonMw; National Institute of Environmental Health Sciences; Canadian Institutes of Health Research; U.S. Department of Veterans Affairs; National Institute for Health and Care Research; British Heart Foundation; Wellcome Trust","keywords":"Biology; Genome-wide association study; Childhood obesity; Meta-analysis; Genetics; Genetic association; Obesity; Computational biology; Association (psychology); Evolutionary biology; Single-nucleotide polymorphism; Gene; Genotype; Overweight","score_opus":0.03503552564385885,"score_gpt":0.31511608853615797,"score_spread":0.2800805628922991,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1983270011","genre_codex":"review","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":null,"domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.0014433776,0.99457717,0.0016222481,0.0013879801,0.00027430186,0.0000063758725,0.00024765183,0.000026405567,0.00041447094],"genre_scores_gemma":[0.012708838,0.98136365,0.0031018355,0.0011651452,0.0007529712,0.00002250947,0.0004818409,0.000013066751,0.0003902926],"study_design_codex":"design_other","study_design_gemma":"meta_analysis","domain_scores_codex":[0.9991602,0.00021190579,0.00009616106,0.0002791922,0.00020464628,0.000047955764],"domain_scores_gemma":[0.9974693,0.0017522463,0.00028065944,0.00012186958,0.00028445615,0.00009159456],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.003235442,0.0016134568,0.0029071844,0.002025772,0.0002062653,0.0012558014,0.0014393568,0.0013412916,0.0015032765],"category_scores_gemma":[0.0035306315,0.0005112294,0.001960439,0.003204618,0.00043651432,0.0006547783,0.0009280894,0.0018664232,0.00043330196],"study_design_candidate":"meta_analysis","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0009489215,0.00007471943,0.025627114,0.013785563,0.013550344,0.00086395297,0.000056156172,0.0007830268,0.0024937815,0.0021255503,0.02246922,0.9172217],"study_design_scores_gemma":[0.0009696229,0.00077117386,0.23099466,0.020218167,0.083742104,0.013671069,0.00039179783,0.0022993365,0.0061933813,0.029564913,0.6107244,0.00045931744],"about_ca_topic_score_codex":0.0025418955,"about_ca_topic_score_gemma":0.0062641595,"teacher_disagreement_score":0.003235442,"about_ca_system_score_codex":0.00062829396,"about_ca_system_score_gemma":0.0015407086,"threshold_uncertainty_score":0.017110884},"labels":[],"label_agreement":null},{"id":"W1984497969","doi":"10.1038/ng.593","title":"Lin28a transgenic mice manifest size and puberty phenotypes identified in human genetic association studies","year":2010,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Plant Molecular Biology Research","field":"Agricultural and Biological Sciences","cited_by":314,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Hospital for Sick Children; University of Toronto","funders":"Eunice Kennedy Shriver National Institute of Child Health and Human Development; National Cancer Institute; National Institutes of Health; Howard Hughes Medical Institute","keywords":"Biology; LIN28; Phenotype; Caenorhabditis elegans; Transgene; Genetics; Ribosome biogenesis; microRNA; Epigenetics; Gene; Induced pluripotent stem cell; RNA; Embryonic stem cell","score_opus":0.014417162721374253,"score_gpt":0.2786616619867575,"score_spread":0.26424449926538324,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1984497969","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.97241634,0.0010379493,0.013628945,0.000705042,0.000322214,0.00007460795,0.0043689404,0.0017501396,0.0056958306],"genre_scores_gemma":[0.9605698,0.00096850743,0.011533202,0.00040032668,0.00013063585,0.0002523086,0.0024969457,0.0013946175,0.022253616],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9994796,0.00006900681,0.000044193548,0.0001590512,0.00017905337,0.000069108166],"domain_scores_gemma":[0.9984054,0.00033671345,0.0006401947,0.0001320572,0.00006226144,0.00042338946],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00039859972,0.001053657,0.0006283108,0.0022476397,0.0005222903,0.00048523516,0.00080190663,0.0013591679,0.013388673],"category_scores_gemma":[0.0005533625,0.0005758486,0.0004879704,0.0006089195,0.0013429789,0.0003691748,0.00083143904,0.0017271774,0.0020187777],"study_design_candidate":"bench_or_experimental","study_design_consensus":"bench_or_experimental","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00031648832,0.00008739677,0.00094247976,0.000025710342,0.000015943586,0.00097397406,0.00005437442,0.000067765905,0.9947246,0.000488925,0.00029334045,0.002009136],"study_design_scores_gemma":[0.00057628046,0.00052908954,0.09088518,0.000051310883,0.00019435551,0.02271269,0.0002868969,0.0019627993,0.86365664,0.0020650746,0.016987063,0.00009261547],"about_ca_topic_score_codex":0.0006870682,"about_ca_topic_score_gemma":0.00142394,"teacher_disagreement_score":0.013388673,"about_ca_system_score_codex":0.00025608114,"about_ca_system_score_gemma":0.00034226617,"threshold_uncertainty_score":0.044789553},"labels":[],"label_agreement":null},{"id":"W1985549353","doi":"10.1038/ng921","title":"Mutant DNA-binding domain of HSF4 is associated with autosomal dominant lamellar and Marner cataract","year":2002,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Heat shock proteins research","field":"Biochemistry, Genetics and Molecular Biology","cited_by":275,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of British Columbia; Xenon Pharmaceuticals (Canada)","funders":"","keywords":"Biology; Genetics; Missense mutation; Locus (genetics); Cataracts; Mutant; Gene; Mutation","score_opus":0.008646077485499665,"score_gpt":0.25257897627794884,"score_spread":0.24393289879244917,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1985549353","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9956949,0.00042498045,0.0019242112,0.00024003645,0.00010799951,0.000028569684,0.00050047436,0.00016240455,0.00091638113],"genre_scores_gemma":[0.9972139,0.00013937462,0.0007235434,0.00006592544,0.000048950715,0.000018184077,0.00027021542,0.000048100206,0.0014716493],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9995498,0.00010254004,0.00007828364,0.000079336314,0.00011915823,0.0000708997],"domain_scores_gemma":[0.9986527,0.00043089996,0.00043484982,0.0001004799,0.00007540957,0.00030566403],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0003498796,0.0016796915,0.000760733,0.0014283098,0.00070766127,0.00033906978,0.0009949887,0.0013752347,0.005540866],"category_scores_gemma":[0.0009174205,0.00046324806,0.001004982,0.0006897381,0.0013526651,0.0002975613,0.0008272495,0.001195725,0.00080386375],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0032728591,0.00033121856,0.006503903,0.00022886369,0.0004702021,0.071454324,0.000348252,0.0009178606,0.9095301,0.0017848598,0.0009956055,0.0041618133],"study_design_scores_gemma":[0.0011953685,0.0017210005,0.14718747,0.00010928505,0.001200861,0.24645373,0.00068226183,0.011942456,0.57466954,0.0029912083,0.011567543,0.00027923673],"about_ca_topic_score_codex":0.0032268907,"about_ca_topic_score_gemma":0.0019722541,"teacher_disagreement_score":0.005540866,"about_ca_system_score_codex":0.00049722655,"about_ca_system_score_gemma":0.000450854,"threshold_uncertainty_score":0.01853609},"labels":[],"label_agreement":null},{"id":"W1985742486","doi":"10.1038/ng.666","title":"Common variants at 19p13 are associated with susceptibility to ovarian cancer","year":2010,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Ovarian cancer diagnosis and treatment","field":"Medicine","cited_by":257,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Simon Fraser University; Alberta Health Services; BC Cancer Agency; Coalition for Research in Women's Health","funders":"National Cancer Institute; National Institutes of Health; Cancer Research UK; Wellcome Trust","keywords":"Ovarian cancer; Biology; Single-nucleotide polymorphism; Genome-wide association study; Locus (genetics); Serous fluid; Epithelial ovarian cancer; Malignancy; Gene; Candidate gene; Genetic association; Oncology; Cancer; Internal medicine; Genetics; Genotype; Medicine","score_opus":0.012029095205191322,"score_gpt":0.2917239398868368,"score_spread":0.2796948446816455,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1985742486","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9925442,0.0022186986,0.001353245,0.0005348894,0.000119769786,0.000029012746,0.0014479568,0.00007178197,0.0016804483],"genre_scores_gemma":[0.995987,0.0008248435,0.0011854828,0.000101126134,0.00015749643,0.000019555235,0.0006911047,0.000043915396,0.0009896134],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99901724,0.0002412245,0.00013739799,0.00023903452,0.00024044793,0.0001246267],"domain_scores_gemma":[0.9957837,0.0017224394,0.0016863028,0.00017963821,0.00019288952,0.00043503285],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00053176255,0.0012049582,0.00095188286,0.003238745,0.0007361293,0.0007187798,0.0009937813,0.0015301221,0.0072437897],"category_scores_gemma":[0.0038951926,0.0006092539,0.0012684797,0.004484555,0.0007208638,0.00037789613,0.00079028873,0.0010374305,0.0005843413],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.007560561,0.00022565488,0.826807,0.00025252317,0.0030849806,0.039045215,0.0004828159,0.0016493738,0.086457,0.0011945252,0.0022617034,0.03097851],"study_design_scores_gemma":[0.00035390348,0.00043535768,0.95441073,0.00007633463,0.0011899883,0.029739697,0.00020064735,0.0011952396,0.0075821723,0.0018012287,0.002956175,0.000058431477],"about_ca_topic_score_codex":0.0024289398,"about_ca_topic_score_gemma":0.0025534919,"teacher_disagreement_score":0.0072437897,"about_ca_system_score_codex":0.0003641878,"about_ca_system_score_gemma":0.00033486646,"threshold_uncertainty_score":0.024232864},"labels":[],"label_agreement":null},{"id":"W1986265706","doi":"10.1038/ng1337","title":"The effects of human population structure on large genetic association studies","year":2004,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Genetic Associations and Epidemiology","field":"Biochemistry, Genetics and Molecular Biology","cited_by":900,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"McGill University; McGill Genome Centre","funders":"National Institutes of Health; Wellcome Trust","keywords":"Biology; Genetic association; Population; Genome-wide association study; Single-nucleotide polymorphism; Population stratification; Genetics; Population structure; Sample size determination; Association (psychology); Evolutionary biology; Computational biology; Demography; Genotype; Statistics; Gene","score_opus":0.005188524372150809,"score_gpt":0.29235825972629786,"score_spread":0.2871697353541471,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1986265706","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9040026,0.031284615,0.04248805,0.010621711,0.000526774,0.00009932559,0.0016335077,0.00051578996,0.008827623],"genre_scores_gemma":[0.99199206,0.0015491516,0.003943601,0.0009970398,0.00048051254,0.000031686315,0.0003106401,0.0001006127,0.0005947741],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.8791271,0.099946156,0.0031882147,0.009450676,0.006586536,0.0017012757],"domain_scores_gemma":[0.4733371,0.45256236,0.017207582,0.04759325,0.006438716,0.0028609992],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.07828285,0.0010675086,0.0022687302,0.0039307764,0.0018646094,0.003343147,0.0021396056,0.0030149207,0.0024735664],"category_scores_gemma":[0.23762305,0.001567006,0.0023366571,0.005143382,0.0077929855,0.003174641,0.0036973753,0.0045127864,0.00033948573],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0016604989,0.00010868222,0.9191042,0.00030285475,0.009036466,0.0012876109,0.0013526758,0.0066707204,0.0034740854,0.012782554,0.0022833038,0.041936323],"study_design_scores_gemma":[0.00019758286,0.00027546543,0.9423722,0.000115838586,0.0050929743,0.0014180955,0.00027016064,0.0074445033,0.0008157269,0.03909842,0.0027905973,0.00010840173],"about_ca_topic_score_codex":0.006911414,"about_ca_topic_score_gemma":0.012018012,"teacher_disagreement_score":0.07828285,"about_ca_system_score_codex":0.0009550465,"about_ca_system_score_gemma":0.00083254103,"threshold_uncertainty_score":0.4140042},"labels":[],"label_agreement":null},{"id":"W1986997900","doi":"10.1038/ng1065","title":"Birc1e is the gene within the Lgn1 locus associated with resistance to Legionella pneumophila","year":2002,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Legionella and Acanthamoeba research","field":"Biochemistry, Genetics and Molecular Biology","cited_by":281,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Ottawa; McGill University","funders":"","keywords":"Biology; Legionella pneumophila; Locus (genetics); Genetics; Gene; Molecular biology; Microbiology; Bacteria","score_opus":0.011689287496330083,"score_gpt":0.24570459451554894,"score_spread":0.23401530701921885,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1986997900","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9652475,0.0050370074,0.014249149,0.00052656606,0.00027282673,0.000081355174,0.0036724408,0.0010463326,0.0098668225],"genre_scores_gemma":[0.9830177,0.00063254684,0.0054033725,0.00017513655,0.000016306589,0.00002494129,0.0036949988,0.00010418282,0.0069308425],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9998884,0.0000113226515,0.0000050489843,0.00003078479,0.00003335023,0.00003108725],"domain_scores_gemma":[0.9998714,0.00002089314,0.00003225179,0.00000947541,0.000017644734,0.000048319678],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.000096863,0.00043762277,0.00036065967,0.0006709353,0.00052144413,0.00047341097,0.0003547049,0.00059360603,0.0021423805],"category_scores_gemma":[0.00021774344,0.00017590215,0.00018869038,0.00038846972,0.00055319,0.00021912677,0.0003511546,0.0006135084,0.001483483],"study_design_candidate":"bench_or_experimental","study_design_consensus":"bench_or_experimental","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00024401388,0.000036113557,0.0011777021,0.00007010342,0.0000072156195,0.00054259575,0.000025053041,0.00014453223,0.99004924,0.0005727519,0.0005694881,0.006561169],"study_design_scores_gemma":[0.00006124864,0.00010934382,0.054176424,0.00004046188,0.000027402644,0.0037924862,0.00011922434,0.0017684229,0.9089976,0.0006576051,0.030209,0.000040810355],"about_ca_topic_score_codex":0.0019365842,"about_ca_topic_score_gemma":0.0024557763,"teacher_disagreement_score":0.0021423805,"about_ca_system_score_codex":0.0009979064,"about_ca_system_score_gemma":0.0003219834,"threshold_uncertainty_score":0.0072402954},"labels":[],"label_agreement":null},{"id":"W1987279431","doi":"10.1038/ng.2254","title":"Mutations in the RNA exosome component gene EXOSC3 cause pontocerebellar hypoplasia and spinal motor neuron degeneration","year":2012,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Extracellular vesicles in disease","field":"Biochemistry, Genetics and Molecular Biology","cited_by":262,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Children's Hospital of Winnipeg; Hospital for Sick Children; SickKids Foundation; University of Toronto; Mount Sinai Hospital; University of Manitoba","funders":"National Institute of Arthritis and Musculoskeletal and Skin Diseases; National Institute of Neurological Disorders and Stroke; National Eye Institute","keywords":"Biology; Spinal muscular atrophy; Genetics; Exosome complex; Exon; Zebrafish; Maldevelopment; Motor neuron; RNA; Gene; Neuroscience; Non-coding RNA; Spinal cord; Anatomy","score_opus":0.011984150582202901,"score_gpt":0.2642681460963528,"score_spread":0.2522839955141499,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1987279431","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99475104,0.00032667865,0.002226527,0.00024116092,0.00008103479,0.000025898078,0.00054804044,0.00019595101,0.0016036944],"genre_scores_gemma":[0.9965519,0.00017699739,0.0015684958,0.00006547985,0.000018740677,0.0000113730075,0.00025478387,0.000076679375,0.0012754791],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9997272,0.000021059794,0.000028368471,0.000057014575,0.00013280164,0.00003363523],"domain_scores_gemma":[0.9994604,0.0001384945,0.00020262795,0.000025628195,0.00002757592,0.0001453345],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00012326322,0.0013440825,0.00048142273,0.0009805158,0.0004848983,0.00035419822,0.00046430333,0.0016089695,0.0022189252],"category_scores_gemma":[0.0005195108,0.00036287174,0.00048306934,0.00058489764,0.001335694,0.000261513,0.0006574124,0.0009027997,0.00041426756],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0004519255,0.00007191536,0.005623719,0.00009474893,0.00013028884,0.037261225,0.00017012343,0.0007634907,0.9488087,0.0007947751,0.00060599967,0.00522301],"study_design_scores_gemma":[0.00032157445,0.00041215753,0.21209,0.000084563704,0.0003851037,0.14475602,0.00046850514,0.006390815,0.62509257,0.0022310996,0.007623509,0.00014410737],"about_ca_topic_score_codex":0.0037268254,"about_ca_topic_score_gemma":0.007715769,"teacher_disagreement_score":0.0037268254,"about_ca_system_score_codex":0.0007502117,"about_ca_system_score_gemma":0.0006709107,"threshold_uncertainty_score":0.0074230433},"labels":[],"label_agreement":null},{"id":"W1987311809","doi":"10.1038/ng.2855","title":"Germline loss-of-function mutations in LZTR1 predispose to an inherited disorder of multiple schwannomas","year":2013,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Neurofibromatosis and Schwannoma Cases","field":"Medicine","cited_by":322,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Lakeridge Health; University of British Columbia","funders":"National Institute of Arthritis and Musculoskeletal and Skin Diseases; National Cancer Institute; University of Alabama at Birmingham; Children's Tumor Foundation","keywords":"Loss of heterozygosity; Germline mutation; Germline; SMARCB1; Genetics; Biology; Mutation; Neurofibromatosis type 2; Allele; Gene; Neurofibromatosis","score_opus":0.013827401036419806,"score_gpt":0.2781015929123892,"score_spread":0.26427419187596934,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1987311809","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.994131,0.0002961946,0.0010495029,0.00037835448,0.000043282045,0.000024875631,0.00012392728,0.000105407984,0.0038473976],"genre_scores_gemma":[0.99903524,0.000048269838,0.00039999417,0.00003896263,0.000043236294,0.0000034788802,0.000024483152,0.000014263584,0.00039217618],"study_design_codex":"case_report","study_design_gemma":"observational","domain_scores_codex":[0.9995363,0.000048642516,0.00005462348,0.0001095057,0.00014354197,0.000107412656],"domain_scores_gemma":[0.99894077,0.0003718056,0.0003483943,0.000048398477,0.00006770892,0.00022282799],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0002945575,0.0016216811,0.00049852615,0.0021990803,0.0011195473,0.0007867575,0.0007966149,0.0017655755,0.0043677473],"category_scores_gemma":[0.0018941505,0.00042768568,0.00062888797,0.00096255506,0.0010722787,0.00050391257,0.00084244757,0.00080780376,0.00090392766],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.000494471,0.00011402208,0.03635969,0.00006175505,0.00007444798,0.8672756,0.0006460385,0.00056324166,0.08897158,0.0011986408,0.00050504314,0.003735472],"study_design_scores_gemma":[0.00006750171,0.00022161746,0.05572528,0.000029742889,0.00014323089,0.92663723,0.00039586748,0.0016146926,0.013586835,0.0005017222,0.0010364406,0.00003976987],"about_ca_topic_score_codex":0.0011708824,"about_ca_topic_score_gemma":0.0012513811,"teacher_disagreement_score":0.0043677473,"about_ca_system_score_codex":0.0005163156,"about_ca_system_score_gemma":0.00040401617,"threshold_uncertainty_score":0.014611542},"labels":[],"label_agreement":null},{"id":"W1987678450","doi":"10.1038/ng906","title":"Large-scale prediction of Saccharomyces cerevisiae gene function using overlapping transcriptional clusters","year":2002,"lang":"en","type":"article","venue":"Nature Genetics","topic":"RNA and protein synthesis mechanisms","field":"Biochemistry, Genetics and Molecular Biology","cited_by":351,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Toronto","funders":"","keywords":"Biology; Computational biology; Saccharomyces cerevisiae; Genome; Functional genomics; Genomics; Gene; Genetics; Ribosomal protein; Gene prediction; RNA; Ribosome","score_opus":0.014813864753072763,"score_gpt":0.226052024700641,"score_spread":0.21123815994756825,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1987678450","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.88297904,0.00077136734,0.10834307,0.0001017998,0.000028715485,0.00008016477,0.0044052633,0.002261507,0.0010291628],"genre_scores_gemma":[0.92599744,0.00028870613,0.05929136,0.000026124084,0.000014530512,0.00006515788,0.013574624,0.00017326257,0.0005687632],"study_design_codex":"bench_or_experimental","study_design_gemma":"simulation_or_modeling","domain_scores_codex":[0.999828,0.00003579768,0.00001336003,0.00006544698,0.000035898633,0.000021522435],"domain_scores_gemma":[0.9995154,0.00021476686,0.00004588057,0.000055586108,0.00010167222,0.00006667458],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0004106332,0.0009570911,0.0007457994,0.0009828475,0.00059445784,0.0007283117,0.000473058,0.00043616453,0.0007322105],"category_scores_gemma":[0.0010232598,0.00035924005,0.00079935277,0.0008949984,0.00023820737,0.00036358903,0.0003231477,0.00060916354,0.00059203216],"study_design_candidate":"simulation_or_modeling","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.003989691,0.0005001529,0.021172188,0.000497748,0.00021644698,0.0008686577,0.00020306841,0.1760388,0.7242838,0.005198407,0.0024105024,0.06462057],"study_design_scores_gemma":[0.00027124412,0.00035931665,0.019191148,0.000030075556,0.00019931114,0.00028260314,0.0001906931,0.81347656,0.15681288,0.00533699,0.0038064201,0.000042727283],"about_ca_topic_score_codex":0.0036246774,"about_ca_topic_score_gemma":0.005202039,"teacher_disagreement_score":0.0036246774,"about_ca_system_score_codex":0.0007460639,"about_ca_system_score_gemma":0.0008696297,"threshold_uncertainty_score":0.007207155},"labels":[],"label_agreement":null},{"id":"W1987824870","doi":"10.1038/ng1927","title":"Mutations in SYNE1 lead to a newly discovered form of autosomal recessive cerebellar ataxia","year":2006,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Genetic Neurodegenerative Diseases","field":"Neuroscience","cited_by":347,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Université Laval; Hôpital de l'Enfant-Jésus; Université de Montréal; Centre Hospitalier de l’Université de Montréal","funders":"McGill University","keywords":"Spinocerebellar ataxia; Ataxia; Genetics; Biology; Cerebellar ataxia; Ataxia-telangiectasia; Gene; Neuroscience","score_opus":0.013408219356834635,"score_gpt":0.27461280362246693,"score_spread":0.2612045842656323,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1987824870","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.98729336,0.0010874211,0.0059628054,0.0006875752,0.00022965106,0.00006744888,0.00062329794,0.00040332548,0.0036452177],"genre_scores_gemma":[0.99298877,0.00050968665,0.0033204425,0.00015271042,0.000060301307,0.00001868227,0.0004266913,0.000059166287,0.002463733],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9997943,0.000026033573,0.000030194664,0.000046623954,0.00007662032,0.000026214497],"domain_scores_gemma":[0.9995266,0.00015972933,0.00014594542,0.00002804352,0.000034263565,0.000105306164],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00028952857,0.0015741012,0.000629503,0.0007270617,0.000501444,0.00045468917,0.00057226396,0.0016082604,0.0012863294],"category_scores_gemma":[0.0007140151,0.00036777745,0.00045159893,0.00045053908,0.00086463336,0.00030998778,0.00067796715,0.00078645773,0.00048453143],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0011091504,0.00025734972,0.009542294,0.00018909207,0.00021008759,0.25137013,0.00040040453,0.0014958765,0.71275455,0.003928379,0.003160477,0.015582151],"study_design_scores_gemma":[0.0007011167,0.0011789096,0.08243334,0.0000857163,0.00052356045,0.5647669,0.00040153918,0.0109364325,0.31277165,0.003043494,0.02297964,0.00017772794],"about_ca_topic_score_codex":0.00065700395,"about_ca_topic_score_gemma":0.0014676263,"teacher_disagreement_score":0.0016082604,"about_ca_system_score_codex":0.00042944215,"about_ca_system_score_gemma":0.0003541729,"threshold_uncertainty_score":0.004303217},"labels":[],"label_agreement":null},{"id":"W1988832105","doi":"10.1038/ng.2684","title":"An atlas of over 90,000 conserved noncoding sequences provides insight into crucifer regulatory regions","year":2013,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Genomics and Phylogenetic Studies","field":"Biochemistry, Genetics and Molecular Biology","cited_by":403,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"McGill University; University of Toronto","funders":"European Regional Development Fund; Grantová Agentura České Republiky; Nederlandse Organisatie voor Wetenschappelijk Onderzoek; Joint Genome Institute; Genome Canada; Génome Québec; U.S. Department of Energy; National Science Foundation","keywords":"Biology; Negative selection; Crucifer; Genome; Genetics; Genomics; DNA sequencing; Gene; Conserved sequence; Evolutionary biology; Arabidopsis thaliana; Population; Noncoding DNA; Computational biology; Botany","score_opus":0.010885955576740615,"score_gpt":0.25211930363203267,"score_spread":0.24123334805529206,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1988832105","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.7728429,0.040310547,0.07490278,0.0005736282,0.00032398122,0.00013924907,0.08631102,0.005983314,0.018612677],"genre_scores_gemma":[0.7357221,0.025925314,0.09129419,0.00057266484,0.0001979405,0.00024109663,0.12966295,0.0009397818,0.0154439565],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.99984944,0.000009902472,0.000013014395,0.00006349079,0.00004203122,0.000022030987],"domain_scores_gemma":[0.9996113,0.000078905796,0.00011370727,0.000041474774,0.00007260684,0.0000820539],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00017765736,0.0007105126,0.00060257915,0.0020409652,0.0007424626,0.0005659026,0.00034511022,0.00030677667,0.0024286278],"category_scores_gemma":[0.0003464937,0.0002242072,0.00036750053,0.003376043,0.00017751192,0.00046254028,0.00032265822,0.0005385279,0.0014384422],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0003741473,0.00003131409,0.007480181,0.00094984175,0.00010489803,0.000683617,0.00039521485,0.00072825816,0.8885389,0.0019561355,0.0039486224,0.09480891],"study_design_scores_gemma":[0.00005982471,0.0003696876,0.32129404,0.0005626675,0.00089529477,0.0054257005,0.0008753129,0.006612624,0.22331516,0.01218235,0.42819968,0.0002077875],"about_ca_topic_score_codex":0.0020734142,"about_ca_topic_score_gemma":0.004666425,"teacher_disagreement_score":0.0024286278,"about_ca_system_score_codex":0.0003453556,"about_ca_system_score_gemma":0.0005707015,"threshold_uncertainty_score":0.00812453},"labels":[],"label_agreement":null},{"id":"W1988839887","doi":"10.1038/ng1013","title":"Frequent somatic mutations in PTEN and TP53 are mutually exclusive in the stroma of breast carcinomas","year":2002,"lang":"en","type":"article","venue":"Nature Genetics","topic":"PI3K/AKT/mTOR signaling in cancer","field":"Biochemistry, Genetics and Molecular Biology","cited_by":422,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Manitoba","funders":"","keywords":"PTEN; Biology; Stroma; Loss of heterozygosity; Tensin; Cancer research; Somatic cell; Stromal cell; Epithelium; Genetics; Gene; Immunology; Signal transduction; PI3K/AKT/mTOR pathway","score_opus":0.010276864471940615,"score_gpt":0.24748129090751603,"score_spread":0.2372044264355754,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1988839887","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99863523,0.0004485087,0.00024098167,0.000040287097,0.0000047130466,0.0000022994036,0.0000623343,0.000014657281,0.00055091985],"genre_scores_gemma":[0.9995622,0.00014728622,0.00009779831,0.000009762921,0.000007858175,0.0000016072844,0.000048005633,0.0000028182717,0.0001226283],"study_design_codex":"observational","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9996438,0.000050442,0.00004133728,0.000059512284,0.00012996669,0.00007493077],"domain_scores_gemma":[0.99911946,0.00022007273,0.0003675472,0.00005801139,0.00010240424,0.00013244084],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00029798402,0.000175877,0.0002301119,0.001525424,0.00028504524,0.00044881203,0.00022465036,0.00027171205,0.0013720668],"category_scores_gemma":[0.0015199084,0.00026198517,0.00014453828,0.00072394666,0.00034522146,0.00023772115,0.00044502493,0.00019511297,0.00023238861],"study_design_candidate":"bench_or_experimental","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0015531309,0.0000582401,0.48835683,0.000080465514,0.00012442187,0.008540619,0.00021861575,0.00025814265,0.48250827,0.00034445344,0.00029945548,0.017657405],"study_design_scores_gemma":[0.00003467879,0.00016305501,0.9123002,0.000011581218,0.0001452334,0.045463804,0.00032593787,0.0010005581,0.03875272,0.00047261687,0.0013147636,0.000014846177],"about_ca_topic_score_codex":0.0004469538,"about_ca_topic_score_gemma":0.00084346486,"teacher_disagreement_score":0.001525424,"about_ca_system_score_codex":0.00014035052,"about_ca_system_score_gemma":0.0002141414,"threshold_uncertainty_score":0.0045900345},"labels":[],"label_agreement":null},{"id":"W1988886385","doi":"10.1038/ng.3154","title":"Common variation in PHACTR1 is associated with susceptibility to cervical artery dissection","year":2014,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Connective tissue disorders research","field":"Biochemistry, Genetics and Molecular Biology","cited_by":233,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"McGill University and Génome Québec Innovation Centre","funders":"European Regional Development Fund; National Institutes of Health; Stiftung zur Erforschung der Vaskulären Demenz; Centre hospitalier régional universitaire de Lille; Vlaamse regering; Aarne ja Aili Turusen Säätiö; Exzellenzclusters Entzündungsforschung; Schweizerische Akademie der Medizinischen Wissenschaften; Maud Kuistilan Muistosäätiö; Emil Aaltosen Säätiö; Schweizerische Herzstiftung; Suomen Lääketieteen Säätiö; Päivikki ja Sakari Sohlbergin Säätiö; American Stroke Association; Biomedicum Helsinki-säätiö; Fonds Wetenschappelijk Onderzoek; Schweizerischer Nationalfonds zur Förderung der Wissenschaftlichen Forschung; Institut National de la Santé et de la Recherche Médicale; Fondation Leducq; Agence Nationale de la Recherche; Fondation de France; Instituto de Salud Carlos III; Aarne Koskelon Säätiö; Alfred Kordelinin Säätiö; National Science Foundation; American Heart Association; Helsingin ja Uudenmaan Sairaanhoitopiiri; Deutsche Forschungsgemeinschaft; Eli Lilly and Company","keywords":"Cervical Artery; Genome-wide association study; Biology; Odds ratio; Stroke (engine); Population; Genetic association; Internal medicine; Genetics; Single-nucleotide polymorphism; Dissection (medical); Genotype; Medicine; Anatomy; Gene","score_opus":0.007873351759838082,"score_gpt":0.2904841459593108,"score_spread":0.28261079419947277,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1988886385","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99550253,0.0005103117,0.0011966056,0.0002421112,0.00007172947,0.000022306423,0.0008308549,0.00005651424,0.0015671939],"genre_scores_gemma":[0.9974382,0.00011736026,0.00083204656,0.00010275045,0.00006942088,0.000014564234,0.00046681505,0.00004696893,0.00091175863],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9987233,0.00034747904,0.00016565452,0.00045598333,0.00016997053,0.00013752365],"domain_scores_gemma":[0.99652714,0.0015031719,0.0011641145,0.00025616042,0.00015915559,0.00039025428],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0005817453,0.0012099117,0.00069318915,0.0022615357,0.0007628963,0.0006413678,0.0010583794,0.0016197014,0.009737902],"category_scores_gemma":[0.0024006653,0.00040780747,0.0012378998,0.0018633264,0.00068056857,0.00037032232,0.0006043176,0.0012460757,0.00085143046],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.006358021,0.00055335375,0.5829477,0.00036304194,0.0032520036,0.030236902,0.0014620728,0.0017417157,0.3477279,0.002097891,0.0027672176,0.020492215],"study_design_scores_gemma":[0.00020044901,0.0004285519,0.9653148,0.0001272696,0.0007750269,0.020216212,0.00028451564,0.0023932918,0.00695983,0.0009066696,0.002308129,0.000085234955],"about_ca_topic_score_codex":0.002386368,"about_ca_topic_score_gemma":0.002270784,"teacher_disagreement_score":0.009737902,"about_ca_system_score_codex":0.00030253755,"about_ca_system_score_gemma":0.0002463688,"threshold_uncertainty_score":0.03257656},"labels":[],"label_agreement":null},{"id":"W1989032379","doi":"10.1038/ng.2933","title":"Gain-of-function mutations in IFIH1 cause a spectrum of human disease phenotypes associated with upregulated type I interferon signaling","year":2014,"lang":"en","type":"article","venue":"Nature Genetics","topic":"interferon and immune responses","field":"Immunology and Microbiology","cited_by":591,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"McMaster University; McMaster Children's Hospital","funders":"National Heart, Lung, and Blood Institute","keywords":"Interferon; Biology; Downregulation and upregulation; MDA5; Interferon type I; Phenotype; Immune system; Mutant; Mutation; Wild type; Gene; Signal transduction; microRNA; RNA; Genetics; Cancer research; RNA interference","score_opus":0.009976293019380805,"score_gpt":0.25078415807439763,"score_spread":0.24080786505501683,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1989032379","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99292,0.0007772544,0.002747658,0.00032211124,0.00008370238,0.000035268073,0.0007366537,0.00023708584,0.0021403115],"genre_scores_gemma":[0.9978054,0.00019178305,0.0010794802,0.000067955945,0.000028716953,0.000014534403,0.00026538168,0.000039991322,0.00050678314],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9998512,0.000024451794,0.000019906487,0.000038638453,0.000038123893,0.000027639451],"domain_scores_gemma":[0.99968874,0.000095955176,0.00009890458,0.00002912013,0.000012329298,0.00007496145],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00016335485,0.0011060906,0.00045486886,0.0006548648,0.00037470722,0.0002628704,0.00032386507,0.00074930117,0.0023458796],"category_scores_gemma":[0.00045827488,0.00019732231,0.00038985335,0.00043565343,0.00077251944,0.00015973393,0.00049728743,0.0006090855,0.0005180528],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00067601836,0.000086383574,0.0065004393,0.00009561699,0.00009336355,0.023923494,0.00012764972,0.0006877612,0.95661885,0.0011898456,0.0013418113,0.0086588],"study_design_scores_gemma":[0.0005490155,0.00091489364,0.19828087,0.00012098389,0.00051401264,0.25491717,0.0004811046,0.0065001487,0.5186376,0.0039582364,0.01498978,0.00013626735],"about_ca_topic_score_codex":0.0005481087,"about_ca_topic_score_gemma":0.0008895234,"teacher_disagreement_score":0.0023458796,"about_ca_system_score_codex":0.00022093263,"about_ca_system_score_gemma":0.00020995014,"threshold_uncertainty_score":0.007847786},"labels":[],"label_agreement":null},{"id":"W1989111033","doi":"10.1038/ng.2939","title":"Low copy number of the salivary amylase gene predisposes to obesity","year":2014,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Pancreatic function and diabetes","field":"Medicine","cited_by":263,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"McGill University and Génome Québec Innovation Centre; McGill University; Ottawa Hospital; McGill Genome Centre; University of Ottawa","funders":"National Human Genome Research Institute; Canadian Institutes of Health Research; Novartis Pharma; National Institutes of Health; Hospital for Sick Children; Ontario Ministry of Research and Innovation; Centre National de la Recherche Scientifique; Stiftelsen för Strategisk Forskning; Institut National de la Santé et de la Recherche Médicale; King's College London; Association Diabète Risque Vasculaire; Fédération Française de Cardiologie; British Skin Foundation; Fondation de France; Novo Nordisk; National Institute for Health and Care Research; Australian Government; Agence Nationale de la Recherche; Biotechnology and Biological Sciences Research Council; Imperial College Healthcare NHS Trust; Wellcome Trust; Ontario Genomics; Centre Hospitalier Universitaire de Rennes; Eli Lilly and Company; Genome Canada; Ontario Innovation Trust; Vetenskapsrådet; Brigham and Women's Hospital; Directorate for Biological Sciences; Imperial College London; Medical Research Council; Les Laboratories Pierre Fabre; Qatar Foundation; National Institute of General Medical Sciences; European Renal Association-European Dialysis and Transplant Association; Centre hospitalier régional universitaire de Lille; Ontario Genomics Institute; Sanofi","keywords":"Copy-number variation; Biology; Odds ratio; Obesity; Genetics; Allele; Body mass index; Gene dosage; Genome-wide association study; Gene; Internal medicine; Gene expression; Endocrinology; Single-nucleotide polymorphism; Genotype; Genome; Medicine","score_opus":0.005696118346484886,"score_gpt":0.2560734842389138,"score_spread":0.2503773658924289,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1989111033","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99630487,0.00031254962,0.0014986324,0.0004243973,0.000076730306,0.000012103479,0.00019933248,0.00008083377,0.001090612],"genre_scores_gemma":[0.99844044,0.00017680913,0.0006235745,0.000046451492,0.00007482837,0.000006634698,0.000072461575,0.000031591455,0.00052717066],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9994423,0.00018644224,0.000064230444,0.00012498567,0.00012544518,0.000056562098],"domain_scores_gemma":[0.9985252,0.000652589,0.0004062854,0.00012248941,0.000061319195,0.00023215427],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00033936053,0.0013644529,0.0004885554,0.0027336187,0.00059564994,0.0006804049,0.00068131654,0.0016583414,0.006786161],"category_scores_gemma":[0.0022490376,0.0006643805,0.000694643,0.0010573268,0.00066231954,0.00031877268,0.00061161333,0.0011272465,0.00048640696],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0063598882,0.00077999366,0.32665983,0.00019942554,0.0008605884,0.063027926,0.0012176608,0.0011152698,0.580851,0.0029479158,0.001391756,0.014588734],"study_design_scores_gemma":[0.00029549087,0.0012009845,0.8235784,0.00013659569,0.0011276159,0.12181345,0.0011106157,0.004862797,0.038381066,0.004462969,0.0028658784,0.0001640983],"about_ca_topic_score_codex":0.0008106824,"about_ca_topic_score_gemma":0.00044733807,"teacher_disagreement_score":0.006786161,"about_ca_system_score_codex":0.00021660353,"about_ca_system_score_gemma":0.00019258285,"threshold_uncertainty_score":0.022701979},"labels":[],"label_agreement":null},{"id":"W1989202466","doi":"10.1038/ng0606-610","title":"Predictable trends in protein noise","year":2006,"lang":"en","type":"letter","venue":"Nature Genetics","topic":"Gene Regulatory Network Analysis","field":"Biochemistry, Genetics and Molecular Biology","cited_by":8,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Ottawa","funders":"","keywords":"Biology; Gene expression; Noise (video); Gene; Computational biology; Genetics; Protein expression; Expression (computer science); Evolutionary biology; Cell biology; Computer science; Artificial intelligence","score_opus":0.0041228507975498456,"score_gpt":0.2200913209014485,"score_spread":0.21596847010389866,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1989202466","genre_codex":"commentary","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":null,"domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.10644193,0.015151892,0.15172647,0.6328462,0.033203617,0.000059484635,0.0012609212,0.0023924657,0.056917083],"genre_scores_gemma":[0.8473624,0.006678722,0.015916372,0.093092285,0.021760186,0.00012049753,0.00025945585,0.00044133366,0.014368758],"study_design_codex":"theoretical_or_conceptual","study_design_gemma":"theoretical_or_conceptual","domain_scores_codex":[0.9995951,0.00005916606,0.000021275988,0.00013353523,0.00014784218,0.00004302202],"domain_scores_gemma":[0.9966857,0.0020170724,0.0002581825,0.00046247634,0.00030364175,0.00027294745],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0010074308,0.00031158066,0.000535622,0.0004328431,0.00084143155,0.0013973508,0.00074353063,0.0028018155,0.0033286551],"category_scores_gemma":[0.007653997,0.0003838483,0.0002901177,0.0004022681,0.0022871809,0.0025494474,0.0008602746,0.0044458797,0.0012418099],"study_design_candidate":"theoretical_or_conceptual","study_design_consensus":"theoretical_or_conceptual","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0007416614,0.00008629673,0.004096783,0.00034325584,0.00013613305,0.0025823626,0.0002770069,0.010242251,0.026821278,0.5334934,0.30003738,0.12114211],"study_design_scores_gemma":[0.00017574168,0.00008926366,0.004985676,0.0000576141,0.000044554366,0.0016560281,0.00014894689,0.042130236,0.016502254,0.7942995,0.13982072,0.00008944748],"about_ca_topic_score_codex":0.00035846775,"about_ca_topic_score_gemma":0.0006122304,"teacher_disagreement_score":0.0033286551,"about_ca_system_score_codex":0.00088929717,"about_ca_system_score_gemma":0.00027971613,"threshold_uncertainty_score":0.011135459},"labels":[],"label_agreement":null},{"id":"W1989421786","doi":"10.1038/ng1068","title":"DNMT1 is required to maintain CpG methylation and aberrant gene silencing in human cancer cells","year":2002,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Epigenetics and DNA Methylation","field":"Biochemistry, Genetics and Molecular Biology","cited_by":611,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Parks Canada","funders":"","keywords":"DNMT1; DNA methylation; Biology; Methylation; DNA methyltransferase; Gene silencing; Methyltransferase; Cancer research; CpG site; Tumor suppressor gene; Molecular biology; Cancer epigenetics; Cancer; Carcinogenesis; Gene expression; Gene; Genetics","score_opus":0.015447851940004151,"score_gpt":0.2888930901438567,"score_spread":0.2734452382038526,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1989421786","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9818392,0.0072772177,0.0056087226,0.0005765533,0.000066824185,0.00002335965,0.0011547997,0.0003683524,0.0030849404],"genre_scores_gemma":[0.9949067,0.0009955202,0.0013564125,0.000037981044,0.000008983102,0.000010546291,0.00059964415,0.000029059544,0.0020550333],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99990785,0.000012102292,0.000008103319,0.000021385758,0.000029670124,0.000020882608],"domain_scores_gemma":[0.99984586,0.000029259674,0.000036333982,0.000035173514,0.00002195023,0.00003139997],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0001559324,0.00015669611,0.00029014176,0.00022285154,0.00023549794,0.00045714836,0.00024372639,0.00025806474,0.0012199664],"category_scores_gemma":[0.0004194379,0.00029463167,0.0001641723,0.00022852758,0.00022087806,0.0002090084,0.00025533632,0.00048805156,0.00057929306],"study_design_candidate":"bench_or_experimental","study_design_consensus":"bench_or_experimental","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00020563975,0.000008213063,0.0012428061,0.00005967269,0.00001683327,0.00012270999,0.000029317343,0.00019692902,0.9936639,0.0004802302,0.00018895649,0.0037847564],"study_design_scores_gemma":[0.000025099298,0.00008365403,0.017142667,0.000007065539,0.00003944616,0.00091405667,0.000039556955,0.0015444565,0.97112054,0.0003933968,0.008681986,0.000008035678],"about_ca_topic_score_codex":0.002657277,"about_ca_topic_score_gemma":0.0029079625,"teacher_disagreement_score":0.002657277,"about_ca_system_score_codex":0.0005764664,"about_ca_system_score_gemma":0.00034346269,"threshold_uncertainty_score":0.0052836537},"labels":[],"label_agreement":null},{"id":"W1989568128","doi":"10.1038/ng.2982","title":"An atlas of genetic influences on human blood metabolites","year":2014,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Genetic Associations and Epidemiology","field":"Biochemistry, Genetics and Molecular Biology","cited_by":1645,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"McGill University and Génome Québec Innovation Centre; Jewish General Hospital","funders":"Leibniz-Rechenzentrum; Leibniz-Gemeinschaft; Canadian Institutes of Health Research; Weill Cornell Medical College; National Institutes of Health; Helmholtz Zentrum München; National Institute for Health and Care Research; Bundesministerium für Bildung und Forschung; Bayerische Akademie der Wissenschaften; Münchner Zentrum für Gesundheitswissenschaften; Weill Cornell Medicine - Qatar; Wellcome Trust; Russian Foundation for Basic Research; Qatar Foundation; Deutsche Forschungsgemeinschaft; King's College London; European Commission; Pfizer","keywords":"Biology; Genome-wide association study; Human genetic variation; Genetic variation; Genetic association; Computational biology; Genetics; Human genome; Population; Heritability; Genome; Gene; Single-nucleotide polymorphism; Genotype","score_opus":0.008956332028529091,"score_gpt":0.294727102150822,"score_spread":0.2857707701222929,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1989568128","genre_codex":"dataset","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":null,"domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.14511088,0.14437489,0.115242206,0.0072358213,0.0017810103,0.00026843758,0.41829515,0.018520307,0.1491713],"genre_scores_gemma":[0.44904727,0.17652124,0.13550547,0.0026334657,0.0018453052,0.00038719462,0.16050443,0.0016633471,0.07189231],"study_design_codex":"design_other","study_design_gemma":"observational","domain_scores_codex":[0.9997273,0.00005804668,0.000025803693,0.000078747755,0.000080117185,0.000029981773],"domain_scores_gemma":[0.99878246,0.00046130182,0.00015895769,0.00021067512,0.00024291169,0.00014367906],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0003937824,0.00057686045,0.00054302695,0.0062585813,0.0003684133,0.0010511691,0.00037791254,0.00033396162,0.016947106],"category_scores_gemma":[0.0010792608,0.00029962804,0.00054506335,0.0077222707,0.00021009294,0.0006395116,0.00073525537,0.0005769223,0.003438506],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00086114334,0.0000910812,0.051740643,0.0025775705,0.0010124608,0.0015417123,0.00038416457,0.0054498003,0.038595837,0.021845205,0.1962706,0.6796298],"study_design_scores_gemma":[0.000056131732,0.00017801767,0.3087359,0.00039647784,0.0005311725,0.003913564,0.00020330759,0.0019595684,0.008218041,0.02958681,0.6461211,0.00009989],"about_ca_topic_score_codex":0.005562247,"about_ca_topic_score_gemma":0.010763147,"teacher_disagreement_score":0.016947106,"about_ca_system_score_codex":0.000540061,"about_ca_system_score_gemma":0.00081583933,"threshold_uncertainty_score":0.056693792},"labels":[],"label_agreement":null},{"id":"W1990430353","doi":"10.1038/ng.2852","title":"Meta-analysis of gene-level tests for rare variant association","year":2013,"lang":"en","type":"review","venue":"Nature Genetics","topic":"Genetic Associations and Epidemiology","field":"Biochemistry, Genetics and Molecular Biology","cited_by":222,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Ottawa","funders":"National Human Genome Research Institute; National Institute on Drug Abuse; National Heart, Lung, and Blood Institute; Canadian Institutes of Health Research; National Institutes of Health; Novo Nordisk Fonden; National Eye Institute; Wellcome Trust","keywords":"Meta-analysis; Biology; Genetic association; Exome; Genetics; Computational biology; Sample size determination; Exome sequencing; Gene; Mutation; Genotype; Single-nucleotide polymorphism; Statistics; Medicine; Internal medicine","score_opus":0.11787469927759159,"score_gpt":0.37381277569154464,"score_spread":0.25593807641395305,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1990430353","genre_codex":"review","genre_gemma":"review","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"review","genre_consensus":"review","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.0014772711,0.98555505,0.010675884,0.00091839855,0.00041845595,0.000029790981,0.0004789824,0.00009803419,0.00034810757],"genre_scores_gemma":[0.07231897,0.88638824,0.032039486,0.0033478057,0.0029034002,0.00023588621,0.0018844289,0.00016647109,0.0007153918],"study_design_codex":"design_other","study_design_gemma":"meta_analysis","domain_scores_codex":[0.9860094,0.008628904,0.001465134,0.002116892,0.0015847926,0.0001948632],"domain_scores_gemma":[0.91717505,0.076281056,0.0023605172,0.0020908613,0.0018127664,0.00027965038],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.024336794,0.0023445808,0.009588096,0.0036196315,0.00026334124,0.0018970347,0.0041277204,0.0020150295,0.0030363926],"category_scores_gemma":[0.057025675,0.00109409,0.008801095,0.0047686393,0.0008262864,0.001278545,0.0013133023,0.0025098275,0.00054422906],"study_design_candidate":"meta_analysis","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0024179134,0.000080687896,0.019297723,0.03355328,0.1623829,0.0005426729,0.000070361,0.0037780423,0.0008703015,0.0033371549,0.012488823,0.76118016],"study_design_scores_gemma":[0.0038637528,0.0022474849,0.083784,0.029521031,0.59367317,0.00867505,0.00027016038,0.01679729,0.005006502,0.10370467,0.15181245,0.000644473],"about_ca_topic_score_codex":0.0023816084,"about_ca_topic_score_gemma":0.0046162894,"teacher_disagreement_score":0.024336794,"about_ca_system_score_codex":0.00083979516,"about_ca_system_score_gemma":0.0020747771,"threshold_uncertainty_score":0.12870681},"labels":[],"label_agreement":null},{"id":"W1990725675","doi":"10.1038/ng.2745","title":"Defining the disease liability of variants in the cystic fibrosis transmembrane conductance regulator gene","year":2013,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Cystic Fibrosis Research Advances","field":"Medicine","cited_by":625,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Institute for Clinical Evaluative Sciences; SickKids Foundation; University of Toronto; Public Health Ontario; Hospital for Sick Children","funders":"National Institute of Diabetes and Digestive and Kidney Diseases; National Heart, Lung, and Blood Institute; Science and Engineering Research Board; Cystic Fibrosis Foundation Therapeutics; Cystic Fibrosis Foundation","keywords":"Cystic fibrosis transmembrane conductance regulator; Cystic fibrosis; Biology; Penetrance; Allele; Disease; Genetics; Genotype; Phenotype; Gene; Ivacaftor; Bioinformatics; Internal medicine; Medicine","score_opus":0.008891065869901502,"score_gpt":0.284383094917442,"score_spread":0.2754920290475405,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1990725675","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9862272,0.001339467,0.008021158,0.001210422,0.00005341169,0.000024441999,0.00027416705,0.000028206096,0.0028214478],"genre_scores_gemma":[0.9947432,0.00048107194,0.0038644657,0.0003913244,0.00007357825,0.000010411597,0.00017964057,0.000026050264,0.00023032103],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9983625,0.00079963455,0.0001652205,0.00028611187,0.000252767,0.00013377769],"domain_scores_gemma":[0.99818283,0.0010657542,0.0003708808,0.00008293665,0.0001302191,0.00016734724],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0018560261,0.00065338635,0.0005053838,0.0015724098,0.000517345,0.0008644142,0.00057755667,0.0012762989,0.0008426415],"category_scores_gemma":[0.006550349,0.0001867277,0.00033441023,0.0007419745,0.00083054666,0.0005483355,0.0012580791,0.0011090519,0.00017131702],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0016060541,0.0003189492,0.8099215,0.00016426854,0.0003677243,0.00791272,0.0015830797,0.0030121587,0.09388215,0.013857654,0.0023350173,0.06503873],"study_design_scores_gemma":[0.0002781044,0.0012759818,0.86006945,0.00035510745,0.00082171016,0.039953962,0.0014882605,0.01592978,0.029868647,0.04045506,0.009374725,0.00012913877],"about_ca_topic_score_codex":0.001270844,"about_ca_topic_score_gemma":0.0018172304,"teacher_disagreement_score":0.0018560261,"about_ca_system_score_codex":0.0002310436,"about_ca_system_score_gemma":0.00032035235,"threshold_uncertainty_score":0.0098157525},"labels":[],"label_agreement":null},{"id":"W1990954164","doi":"10.1038/ng.2602","title":"Mutations in STAMBP, encoding a deubiquitinating enzyme, cause microcephaly–capillary malformation syndrome","year":2013,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Vascular Malformations and Hemangiomas","field":"Medicine","cited_by":116,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Ottawa Hospital; University of Toronto; Hospital for Sick Children; McGill University and Génome Québec Innovation Centre; McGill University; Children's Hospital of Eastern Ontario; University of Ottawa","funders":"Eunice Kennedy Shriver National Institute of Child Health and Human Development; National Institute of Neurological Disorders and Stroke; Canadian Institutes of Health Research; National Institute of General Medical Sciences; Cancer Research UK","keywords":"Deubiquitinating enzyme; Microcephaly; Biology; Ubiquitin; Cell biology; Cancer research; PI3K/AKT/mTOR pathway; Genetics; Signal transduction; Gene","score_opus":0.011098743943865409,"score_gpt":0.2647473644961663,"score_spread":0.2536486205523009,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1990954164","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.98933977,0.0008861953,0.0043195295,0.00052233395,0.00009455066,0.000038196024,0.000677571,0.00027848166,0.0038433897],"genre_scores_gemma":[0.99756575,0.00019990555,0.0013012481,0.00004966982,0.00003126479,0.000009231496,0.00012625729,0.000024187915,0.000692453],"study_design_codex":"case_report","study_design_gemma":"observational","domain_scores_codex":[0.9997733,0.000025221249,0.000017948141,0.000036283393,0.00011750842,0.000029715626],"domain_scores_gemma":[0.9994367,0.00024742613,0.0001329034,0.000016381895,0.000024963594,0.00014150988],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00008624621,0.0010890616,0.000295129,0.0014194564,0.00038512808,0.00033181818,0.0003770688,0.0010263411,0.0015614242],"category_scores_gemma":[0.0007904197,0.00023516273,0.0003106123,0.0009439344,0.00085409934,0.00023304185,0.0005136734,0.0005940812,0.00028298027],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0006769596,0.000104486266,0.032994945,0.00018569543,0.00023295113,0.5459989,0.0005973783,0.0020986146,0.38112518,0.0040875603,0.0034281935,0.028469093],"study_design_scores_gemma":[0.00022636197,0.00029657438,0.14195709,0.000058556892,0.0003153975,0.66524804,0.00032754394,0.00992044,0.17003341,0.0026849625,0.008841734,0.000089978676],"about_ca_topic_score_codex":0.0022878763,"about_ca_topic_score_gemma":0.0026750662,"teacher_disagreement_score":0.0022878763,"about_ca_system_score_codex":0.00042941145,"about_ca_system_score_gemma":0.00034212397,"threshold_uncertainty_score":0.0052235126},"labels":[],"label_agreement":null},{"id":"W1991728641","doi":"10.1038/ng.170","title":"Age-related macular degeneration is associated with an unstable ARMS2 (LOC387715) mRNA","year":2008,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Retinal Diseases and Treatments","field":"Medicine","cited_by":406,"is_retracted":false,"has_abstract":false,"route_ca_aff":false,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"","funders":"University of British Columbia","keywords":"Biology; Macular degeneration; Genetics; Retina; Indel; Gene; Molecular biology; Single-nucleotide polymorphism; Genotype; Neuroscience; Ophthalmology","score_opus":0.011750557281908915,"score_gpt":0.26120873881586654,"score_spread":0.24945818153395763,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1991728641","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9964317,0.00047137155,0.0013291278,0.00017234946,0.000089551024,0.000021069716,0.0004065206,0.00007263657,0.0010056252],"genre_scores_gemma":[0.9970783,0.0000916302,0.0009875988,0.00017078481,0.000087497705,0.000028282408,0.00041787667,0.000053790278,0.0010842516],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.99968433,0.000059728376,0.000049124752,0.0000993929,0.00007104687,0.00003642171],"domain_scores_gemma":[0.9993249,0.0001853551,0.00033504947,0.000047973463,0.000030076275,0.00007671623],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00021869928,0.000809693,0.00041336397,0.0011244906,0.00036223076,0.0003613175,0.00047276926,0.0010815741,0.004112126],"category_scores_gemma":[0.0007934648,0.00022418625,0.00058725185,0.00050371257,0.0005099083,0.00019921485,0.000374484,0.00046116384,0.00089067005],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0015765331,0.00012828753,0.015574841,0.000088267734,0.0002111903,0.04483974,0.00019800877,0.0003503023,0.92826724,0.00082467945,0.001250125,0.0066908314],"study_design_scores_gemma":[0.0009114909,0.0017042945,0.41487733,0.000120351455,0.0008039618,0.22232632,0.00040043876,0.0067581846,0.33319768,0.0024025457,0.016294925,0.0002024668],"about_ca_topic_score_codex":0.00063169363,"about_ca_topic_score_gemma":0.0006239161,"teacher_disagreement_score":0.004112126,"about_ca_system_score_codex":0.00024165613,"about_ca_system_score_gemma":0.00013600884,"threshold_uncertainty_score":0.013756454},"labels":[],"label_agreement":null},{"id":"W1991912136","doi":"10.1038/ng.2821","title":"Somatic mutation of CDKN1B in small intestine neuroendocrine tumors","year":2013,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Neuroendocrine Tumor Research Advances","field":"Medicine","cited_by":373,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Toronto; Ontario Institute for Cancer Research; University Health Network","funders":"National Cancer Institute; National Institute for Health and Care Research; Cancer Research UK","keywords":"Biology; Frameshift mutation; Somatic cell; Neuroendocrine tumors; Mutation; Germline mutation; Genetics; Exome; Cancer research; Gene; Cyclin-dependent kinase 6; Cell cycle; Exome sequencing; Cyclin; Endocrinology","score_opus":0.01501826094181791,"score_gpt":0.3044819130113842,"score_spread":0.2894636520695663,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1991912136","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99447244,0.0011855651,0.0004682296,0.0002444607,0.000026666085,0.000008943271,0.00016590994,0.000021140364,0.003406633],"genre_scores_gemma":[0.9989704,0.00029128153,0.00025619403,0.000018247089,0.000006166323,0.0000014370155,0.000050533454,0.0000074654226,0.00039824762],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.99987364,0.000012639313,0.000014413722,0.000024756582,0.000048901864,0.000025604093],"domain_scores_gemma":[0.9998461,0.000039809107,0.000037292273,0.000011229712,0.00001696828,0.00004858146],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00015737128,0.00018723548,0.00017587196,0.0007278513,0.0002751495,0.00040363966,0.00022503409,0.00041046747,0.0021379925],"category_scores_gemma":[0.0006048555,0.00012674005,0.00014211184,0.00035241694,0.00039645802,0.00017265287,0.00024806708,0.00019427891,0.0003105892],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0014027894,0.00008730471,0.19067262,0.00015417127,0.00008598987,0.06176734,0.00020203757,0.0011775873,0.6980982,0.0013176566,0.0013888264,0.043645512],"study_design_scores_gemma":[0.00017130177,0.0003635073,0.42220572,0.000053921616,0.00018505787,0.28250778,0.0005254667,0.0059653614,0.2741079,0.0013738433,0.012500102,0.00004004887],"about_ca_topic_score_codex":0.002210119,"about_ca_topic_score_gemma":0.003229232,"teacher_disagreement_score":0.002210119,"about_ca_system_score_codex":0.00072894804,"about_ca_system_score_gemma":0.00026341958,"threshold_uncertainty_score":0.0071522593},"labels":[],"label_agreement":null},{"id":"W1992005334","doi":"10.1038/ng.2606","title":"Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture","year":2013,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Genetic Associations and Epidemiology","field":"Biochemistry, Genetics and Molecular Biology","cited_by":687,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Lunenfeld-Tanenbaum Research Institute; McMaster University; Ontario Institute for Cancer Research","funders":"National Cancer Institute; National Human Genome Research Institute; National Heart, Lung, and Blood Institute; Australian Research Council; Economic and Social Research Council; National Institutes of Health; Heinz Nixdorf Stiftung; Provincia autonoma di Bolzano - Alto Adige; Diabetestutkimussäätiö; Hjartavernd; Novo Nordisk Fonden; Paavo Nurmen Säätiö; Medical Research Council; Tartu Ülikool; Svenska Kulturfonden; Orionin Tutkimussäätiö; Göteborgs Läkaresällskap; Sydäntutkimussäätiö; Samfundet Folkhälsan; Emil Aaltosen Säätiö; Vetenskapsrådet; National Institute on Alcohol Abuse and Alcoholism; Stockholms Läns Landsting; Päivikki ja Sakari Sohlbergin Säätiö; Centre for Medical Systems Biology; Novo Nordisk; Ministero della Salute; National Institute of Diabetes and Digestive and Kidney Diseases; Turun Yliopistollinen Keskussairaala; Knut och Alice Wallenbergs Stiftelse; National Institute of General Medical Sciences; National Alliance for Research on Schizophrenia and Depression; Nierstichting; British Heart Foundation; Bundesministerium für Bildung und Forschung; European Regional Development Fund; Terveyden ja hyvinvoinnin laitos; Academy of Finland; Erasmus Medisch Centrum; Vrije Universiteit Amsterdam; Stiftelsen för Strategisk Forskning; Universitair Medisch Centrum Groningen; Diabetes Fonds; National Science Foundation; Fondation Leducq; Agence Nationale de la Recherche; Hjärt-Lungfonden; Royal Society; Agency for Science, Technology and Research; Helmholtz Zentrum München; March of Dimes Foundation; Kela; Svenska Läkaresällskapet; Deutsche Forschungsgemeinschaft; European Science Foundation; Fondation pour la Recherche Médicale; Svenska Sällskapet för Medicinsk Forskning; Socialdepartementet; European Commission; NHS Blood and Transplant; Folkhälsanin Tutkimussäätiö; National Institute for Health and Care Research; Wellcome Trust; Cancer Research UK; Ministero dell’Istruzione, dell’Università e della Ricerca; QIMR Berghofer Medical Research Institute; Scottish Government; Yrjö Jahnssonin Säätiö; Cancerfonden; Finska Läkaresällskapet; Foundation for Cardiovascular Research; Division of Cancer Epidemiology and Genetics, National Cancer Institute; Juvenile Diabetes Research Foundation International; Schweizerischer Nationalfonds zur Förderung der Wissenschaftlichen Forschung; Tampereen Tuberkuloosisäätiö; Rijksuniversiteit Groningen; Torsten Söderbergs Stiftelse; Karolinska Institutet; National Health and Medical Research Council; Suomen Kulttuurirahasto; Cedars-Sinai Medical Center; Signe ja Ane Gyllenbergin Säätiö; GlaxoSmithKline; Donald W. Reynolds Foundation; Juho Vainion Säätiö; Susan G. Komen for the Cure","keywords":"Biology; Genetic architecture; Genetics; Genome-wide association study; Genome; Computational biology; Quantitative trait locus; Meta-analysis; Evolutionary biology; Gene; Genotype; Single-nucleotide polymorphism","score_opus":0.017396980508164978,"score_gpt":0.27750696768880373,"score_spread":0.26010998718063877,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1992005334","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9254865,0.03176552,0.031184662,0.0016990422,0.00049094093,0.000058914284,0.0071128476,0.00061171816,0.0015898539],"genre_scores_gemma":[0.9908076,0.0024221318,0.004180856,0.00018506323,0.00012817355,0.00003182776,0.0017692504,0.00009712765,0.00037812605],"study_design_codex":"observational","study_design_gemma":"meta_analysis","domain_scores_codex":[0.9943745,0.0020788233,0.00050954684,0.0020806051,0.00056999637,0.00038643397],"domain_scores_gemma":[0.9924118,0.004338578,0.0009658387,0.001447725,0.00041144516,0.0004245694],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.006264919,0.00255178,0.003023668,0.004464873,0.0009496509,0.0024223065,0.0014813683,0.0013690124,0.0024720046],"category_scores_gemma":[0.008042864,0.0009972584,0.008134025,0.00697596,0.0006937509,0.00096471026,0.0016958436,0.0018814271,0.0003064782],"study_design_candidate":"meta_analysis","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0019909164,0.000084407824,0.86542785,0.00042497859,0.108164825,0.000803519,0.00017465654,0.0013712611,0.0070827953,0.000479098,0.0009766355,0.0130189825],"study_design_scores_gemma":[0.00025126192,0.00029602897,0.92389965,0.00011245008,0.06390866,0.001047077,0.00030725685,0.0043499917,0.0017701379,0.0022204039,0.0017521315,0.000084854575],"about_ca_topic_score_codex":0.0055235466,"about_ca_topic_score_gemma":0.007843979,"teacher_disagreement_score":0.006264919,"about_ca_system_score_codex":0.00045519462,"about_ca_system_score_gemma":0.0008042346,"threshold_uncertainty_score":0.033132493},"labels":[],"label_agreement":null},{"id":"W1992911777","doi":"10.1038/ng.2610","title":"Identification of heart rate–associated loci and their effects on cardiac conduction and rhythm disorders","year":2013,"lang":"en","type":"review","venue":"Nature Genetics","topic":"Heart Rate Variability and Autonomic Control","field":"Medicine","cited_by":320,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Université de Montréal; Montreal Heart Institute","funders":"National Center for Advancing Translational Sciences; National Institute on Drug Abuse; National Institute of Diabetes and Digestive and Kidney Diseases; National Heart, Lung, and Blood Institute; Economic and Social Research Council; Novo Nordisk Fonden; National Institute of General Medical Sciences; Medical Research Council; National Institute for Health and Care Research; British Heart Foundation; Wellcome Trust","keywords":"Biology; Identification (biology); Rhythm; Heart Rhythm; Genetics; Internal medicine; Computational biology; Neuroscience; Medicine; Ecology","score_opus":0.01275176434806001,"score_gpt":0.2884915349852082,"score_spread":0.27573977063714816,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1992911777","genre_codex":"review","genre_gemma":"review","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"review","genre_consensus":"review","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.0008535388,0.996036,0.0009486111,0.00056751113,0.00029091822,0.0000063193143,0.00007822136,0.000021972006,0.0011969318],"genre_scores_gemma":[0.005122326,0.99149805,0.0011106203,0.00048109976,0.00067019835,0.0000102151835,0.00017155579,0.0000058204023,0.0009301016],"study_design_codex":"design_other","study_design_gemma":"systematic_review","domain_scores_codex":[0.9997187,0.00004874879,0.000049316888,0.000077806195,0.00008290155,0.000022431746],"domain_scores_gemma":[0.999368,0.0003714795,0.00011416785,0.00002046306,0.00009362977,0.000032274802],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0006785997,0.0012301608,0.0016861246,0.001891275,0.00014969688,0.0008394891,0.0011085945,0.0013028,0.0031546392],"category_scores_gemma":[0.0012695579,0.0002730984,0.00077595166,0.0016436371,0.00041790077,0.0007567097,0.0006079986,0.0010710822,0.0009408726],"study_design_candidate":"systematic_review","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0002032409,0.00008284031,0.0025903168,0.006697436,0.00064605963,0.0015615154,0.00005718547,0.00058726413,0.0042680176,0.002559321,0.012815829,0.9679309],"study_design_scores_gemma":[0.00022170032,0.0002636334,0.023008484,0.006799893,0.0031185858,0.014880184,0.00019572001,0.0007590206,0.0034055135,0.010552867,0.93666553,0.00012878793],"about_ca_topic_score_codex":0.00093048846,"about_ca_topic_score_gemma":0.0012371688,"teacher_disagreement_score":0.0031546392,"about_ca_system_score_codex":0.00031574108,"about_ca_system_score_gemma":0.00068340014,"threshold_uncertainty_score":0.0105533},"labels":[],"label_agreement":null},{"id":"W1992989994","doi":"10.1038/ng1062","title":"Mutations in SBDS are associated with Shwachman–Diamond syndrome","year":2002,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Blood disorders and treatments","field":"Biochemistry, Genetics and Molecular Biology","cited_by":795,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Toronto; Hospital for Sick Children","funders":"","keywords":"Biology; Pseudogene; Genetics; Gene; Exon; Intron; Conserved sequence; Genome; Peptide sequence","score_opus":0.006130153625328871,"score_gpt":0.22054504883438103,"score_spread":0.21441489520905216,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1992989994","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9915193,0.0011349433,0.0025059213,0.00047762968,0.00012725555,0.000029173607,0.00060125167,0.00013784836,0.003466628],"genre_scores_gemma":[0.99728274,0.00023109344,0.0013253713,0.000094032075,0.000052953656,0.0000096166505,0.00021254734,0.00002921711,0.00076257996],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.99973196,0.000036496596,0.000039796098,0.00006318195,0.000086058084,0.000042508495],"domain_scores_gemma":[0.9992138,0.0003055317,0.00021030872,0.000034471093,0.0000553339,0.00018044034],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00020809965,0.0010551241,0.00066236686,0.0015315004,0.0005217877,0.0004231185,0.00058841833,0.0015517288,0.0044300053],"category_scores_gemma":[0.0012635466,0.00028897155,0.00039876293,0.0008358382,0.0011232118,0.00029731603,0.00057962496,0.0007113273,0.0007196239],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.002367055,0.00024521747,0.07279552,0.00033768924,0.0004395222,0.30904758,0.0010607837,0.0011140945,0.5706442,0.005291056,0.004144892,0.032512408],"study_design_scores_gemma":[0.00080609217,0.0007901264,0.24134834,0.00018882978,0.0008683628,0.5452606,0.0010637769,0.0052211294,0.16712013,0.006522719,0.030631095,0.00017875028],"about_ca_topic_score_codex":0.001997089,"about_ca_topic_score_gemma":0.0014932831,"teacher_disagreement_score":0.0044300053,"about_ca_system_score_codex":0.0002773733,"about_ca_system_score_gemma":0.00032140102,"threshold_uncertainty_score":0.014819801},"labels":[],"label_agreement":null},{"id":"W1993588417","doi":"10.1038/ng.943","title":"Large-scale genome-wide association analysis of bipolar disorder identifies a new susceptibility locus near ODZ4","year":2011,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Genetic Associations and Epidemiology","field":"Biochemistry, Genetics and Molecular Biology","cited_by":1412,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of British Columbia; University of British Columbia Hospital; Princess Margaret Cancer Centre; Centre for Addiction and Mental Health","funders":"National Human Genome Research Institute; National Center for Research Resources; National Institute of Mental Health; National Institutes of Health; Norges Forskningsråd; Wellcome Trust","keywords":"Biology; Genome-wide association study; Locus (genetics); Genetics; Bipolar disorder; Computational biology; Genetic association; Genome; Evolutionary biology; Single-nucleotide polymorphism; Gene; Genotype; Neuroscience","score_opus":0.00839347777540485,"score_gpt":0.2513328806779222,"score_spread":0.24293940290251734,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1993588417","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9976114,0.00027470686,0.0010186873,0.00013737852,0.00002064877,0.000010626784,0.00037996704,0.000034304925,0.000512264],"genre_scores_gemma":[0.99746656,0.00019075097,0.001108742,0.00007168315,0.000022201493,0.000011380538,0.00054640835,0.0000174491,0.000564705],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9997906,0.000036007867,0.00001608686,0.00005874584,0.000057646197,0.000040878327],"domain_scores_gemma":[0.9996203,0.000112815134,0.00013045264,0.000026920683,0.000030414323,0.00007905308],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00028811296,0.00052995107,0.0004355641,0.0015621551,0.00065338326,0.00064313284,0.0005166735,0.0005920736,0.0028977562],"category_scores_gemma":[0.00061349646,0.00031022934,0.00069027103,0.0011590382,0.00041472018,0.00013715151,0.00053239847,0.0007140151,0.000293029],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.006275419,0.00036530543,0.49112922,0.00016750522,0.0010530116,0.007505645,0.0005078467,0.000731444,0.46587834,0.0014635745,0.0016832695,0.023239411],"study_design_scores_gemma":[0.00032102547,0.00026102597,0.9737853,0.000031916563,0.0006328469,0.004770415,0.000281221,0.0015805941,0.01479121,0.0008852739,0.0026267525,0.000032406562],"about_ca_topic_score_codex":0.005006074,"about_ca_topic_score_gemma":0.0054724896,"teacher_disagreement_score":0.005006074,"about_ca_system_score_codex":0.00033263344,"about_ca_system_score_gemma":0.00034028772,"threshold_uncertainty_score":0.0099538565},"labels":[],"label_agreement":null},{"id":"W1994916419","doi":"10.1038/87234","title":"Identifying the role of single-nucleotide polymorphisms in breast cancer risk using microarray and mass spectrometry technologies","year":2001,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Gene expression and cancer classification","field":"Biochemistry, Genetics and Molecular Biology","cited_by":0,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Toronto; Lunenfeld-Tanenbaum Research Institute; Mount Sinai Hospital","funders":"","keywords":"Biology; Single-nucleotide polymorphism; Breast cancer; Computational biology; Microarray; Mass spectrometry; Cancer; Genetics; Bioinformatics; Genotype; Gene; Chromatography; Gene expression","score_opus":0.00933459681307253,"score_gpt":0.2543989006229423,"score_spread":0.24506430380986977,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1994916419","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9763241,0.0033235906,0.01640763,0.0007552916,0.00008356087,0.000025908623,0.0019408059,0.00011701661,0.0010220776],"genre_scores_gemma":[0.96921384,0.0016813634,0.026199603,0.00033809931,0.000092540184,0.00006662737,0.0011901975,0.000017609667,0.0012000942],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9995696,0.00010522667,0.00002770473,0.00011884951,0.00014693769,0.000031680585],"domain_scores_gemma":[0.99934214,0.0003940626,0.0001354731,0.000035275756,0.000056133114,0.00003696025],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0006398655,0.00024019014,0.0005004403,0.0010132355,0.00024405893,0.0006633527,0.00021529997,0.0005661592,0.0007345729],"category_scores_gemma":[0.0010656598,0.00018528757,0.00028765734,0.0009398001,0.0001827302,0.0002636706,0.00012957769,0.0005924287,0.0002826591],"study_design_candidate":"bench_or_experimental","study_design_consensus":"bench_or_experimental","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.000525817,0.00009653567,0.05552445,0.00007185028,0.000116249954,0.000110848225,0.00004094975,0.00046259802,0.92033684,0.00036895007,0.0002859889,0.022058856],"study_design_scores_gemma":[0.00004306434,0.0004792343,0.6060075,0.00001983938,0.0002741959,0.0017814733,0.00011798486,0.014518273,0.37067553,0.0022058194,0.0038295276,0.00004752852],"about_ca_topic_score_codex":0.00088241964,"about_ca_topic_score_gemma":0.0016624444,"teacher_disagreement_score":0.0010132355,"about_ca_system_score_codex":0.0002613597,"about_ca_system_score_gemma":0.00019987811,"threshold_uncertainty_score":0.003383994},"labels":[],"label_agreement":null},{"id":"W1994967480","doi":"10.1038/ng.837","title":"A genome-wide association study of metabolic traits in human urine","year":2011,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Metabolism and Genetic Disorders","field":"Biochemistry, Genetics and Molecular Biology","cited_by":259,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Chenomx (Canada)","funders":"","keywords":"Biology; Genome-wide association study; Locus (genetics); Genetics; Urine; Genotype; Population; Genetic association; Gene; Internal medicine; Single-nucleotide polymorphism; Endocrinology; Medicine","score_opus":0.00948541438714923,"score_gpt":0.2501344897484582,"score_spread":0.24064907536130897,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1994967480","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9984926,0.0003814765,0.0004894772,0.000073346826,0.000015024216,0.0000073435895,0.00024357713,0.000011772518,0.00028526853],"genre_scores_gemma":[0.999099,0.000105659994,0.00037386167,0.000032070788,0.000009901838,0.0000057687876,0.00016248447,0.000007411128,0.00020387971],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99865484,0.0005443058,0.00010807509,0.00039322564,0.00016645141,0.00013309903],"domain_scores_gemma":[0.99833965,0.00067194586,0.00029121005,0.00024439298,0.00019492459,0.00025778828],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0012419233,0.0004325057,0.00056929386,0.0013927367,0.0013084885,0.00089652237,0.00047528086,0.0007556641,0.0014953747],"category_scores_gemma":[0.0029725726,0.0004376428,0.0009462612,0.002159997,0.0005221957,0.0002605752,0.00086026103,0.0007705751,0.00017035723],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0028763914,0.00021401176,0.9475791,0.00007040338,0.0014301746,0.001704989,0.00050257216,0.00019699748,0.038207367,0.00025706724,0.0003452221,0.0066157444],"study_design_scores_gemma":[0.00005775101,0.00021709473,0.99502397,0.000007946062,0.00047661446,0.0016924891,0.00018152736,0.0002771882,0.0014658277,0.00010834781,0.00047585237,0.000015389896],"about_ca_topic_score_codex":0.0065209325,"about_ca_topic_score_gemma":0.0075223586,"teacher_disagreement_score":0.0065209325,"about_ca_system_score_codex":0.0002313145,"about_ca_system_score_gemma":0.0005110102,"threshold_uncertainty_score":0.012965918},"labels":[],"label_agreement":null},{"id":"W1995004385","doi":"10.1038/ng1099","title":"Notch1 functions as a tumor suppressor in mouse skin","year":2003,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Hedgehog Signaling Pathway Studies","field":"Biochemistry, Genetics and Molecular Biology","cited_by":972,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"SickKids Foundation; Hospital for Sick Children; University of Toronto","funders":"","keywords":"Biology; Notch signaling pathway; Carcinogenesis; Cyclin-dependent kinase 8; Notch proteins; Cell biology; Epidermis (zoology); Cellular differentiation; Cancer research; Signal transduction; Tumor suppressor gene; Hes3 signaling axis; Cell fate determination; Gene; Genetics; Transcription factor; Anatomy","score_opus":0.007841342637165093,"score_gpt":0.25307659631231394,"score_spread":0.24523525367514884,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1995004385","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9763472,0.004731321,0.010438636,0.0002542397,0.0000802455,0.000041924774,0.00095621083,0.0004398716,0.0067102774],"genre_scores_gemma":[0.9831472,0.0014014641,0.0033163102,0.000050297054,0.000013486086,0.00002615775,0.00044497807,0.00011737253,0.011482737],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9996934,0.00005726003,0.000025808698,0.00007724493,0.0000928599,0.000053447344],"domain_scores_gemma":[0.9996424,0.000073213894,0.00009489212,0.00006169457,0.000036574093,0.00009125582],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00030163178,0.00063245534,0.00027073303,0.0015439638,0.0003981161,0.00068839354,0.0005298841,0.00054130354,0.001808405],"category_scores_gemma":[0.00021278,0.0005355324,0.0003360746,0.0003702992,0.0005623199,0.00058020395,0.00040178504,0.0008133856,0.0009066581],"study_design_candidate":"bench_or_experimental","study_design_consensus":"bench_or_experimental","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.000081337304,0.000008091785,0.00013914252,0.000015676973,0.0000033525619,0.00006543113,0.000007711816,0.00006575994,0.9987245,0.0003189265,0.000022585327,0.0005474518],"study_design_scores_gemma":[0.0000044791414,0.000026077403,0.0006946398,0.0000017903968,0.0000072982493,0.00026760722,0.000010789755,0.00022829727,0.99800414,0.00006550489,0.0006878459,0.0000015599152],"about_ca_topic_score_codex":0.0010253799,"about_ca_topic_score_gemma":0.0012839444,"teacher_disagreement_score":0.001808405,"about_ca_system_score_codex":0.0005832412,"about_ca_system_score_gemma":0.00021650152,"threshold_uncertainty_score":0.0060496926},"labels":[],"label_agreement":null},{"id":"W1995338672","doi":"10.1038/ng916","title":"Mutations in SUFU predispose to medulloblastoma","year":2002,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Hedgehog Signaling Pathway Studies","field":"Biochemistry, Genetics and Molecular Biology","cited_by":799,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Hospital for Sick Children; Princess Margaret Cancer Centre; Ontario Institute for Cancer Research; University of Toronto","funders":"","keywords":"Smoothened; Biology; Patched; Hedgehog signaling pathway; Sonic hedgehog; Cancer research; Germline; Medulloblastoma; GLI1; PTCH1; GLI2; Hedgehog; Genetics; Tumor suppressor gene; Transcription factor; Germline mutation; Loss of heterozygosity; Signal transduction; Mutation; Gene; Carcinogenesis; Allele","score_opus":0.01055282333795032,"score_gpt":0.26065295301950364,"score_spread":0.2501001296815533,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1995338672","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.994975,0.0006500071,0.0014213055,0.0001419897,0.000053248168,0.000017275795,0.00024079137,0.000097159165,0.00240326],"genre_scores_gemma":[0.9989655,0.0001407824,0.00033652873,0.00001243048,0.000016029224,0.000004621032,0.000058447615,0.000014905355,0.00045061627],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9997116,0.000079610116,0.000030785865,0.000053771077,0.00007003032,0.000054146727],"domain_scores_gemma":[0.9989374,0.0004768732,0.00025844492,0.000081797545,0.00003478714,0.00021076268],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0002451581,0.00083878066,0.00049712963,0.0031103357,0.0006308724,0.00031435554,0.00057093956,0.0008853961,0.0059718606],"category_scores_gemma":[0.0011940906,0.00044515435,0.00049156,0.0010315307,0.0009406248,0.00039259755,0.00063247106,0.00069156295,0.00039226664],"study_design_candidate":"bench_or_experimental","study_design_consensus":"bench_or_experimental","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0027829735,0.0002729267,0.057751987,0.00014409809,0.00030793034,0.050038736,0.0009881575,0.0012069012,0.86905307,0.004738438,0.000559793,0.012154921],"study_design_scores_gemma":[0.00020115929,0.0015148596,0.46458226,0.00006785641,0.00061656855,0.1542822,0.0013053365,0.0045268354,0.35813174,0.004473672,0.010137015,0.00016055278],"about_ca_topic_score_codex":0.0018689728,"about_ca_topic_score_gemma":0.002086154,"teacher_disagreement_score":0.0059718606,"about_ca_system_score_codex":0.0002768322,"about_ca_system_score_gemma":0.00021179831,"threshold_uncertainty_score":0.019977808},"labels":[],"label_agreement":null},{"id":"W1995958002","doi":"10.1038/ng1145","title":"Mutations in a Sar1 GTPase of COPII vesicles are associated with lipid absorption disorders","year":2003,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Nuclear Structure and Function","field":"Biochemistry, Genetics and Molecular Biology","cited_by":387,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Université de Montréal; Centre Hospitalier Universitaire Sainte-Justine","funders":"","keywords":"COPII; Vesicle; Biology; Cell biology; Chylomicron; Intracellular; GTPase; Intracellular transport; COPI; Biogenesis; Transport protein; Vesicular transport protein; GTPase-activating protein; Biochemistry; Secretory pathway; Membrane; G protein; Signal transduction; Cholesterol; Gene; Golgi apparatus; Endoplasmic reticulum; Lipoprotein","score_opus":0.0038310651653687103,"score_gpt":0.21439882372023625,"score_spread":0.21056775855486753,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1995958002","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9931318,0.0007062882,0.0030330166,0.0004971951,0.00018592259,0.000065888606,0.00033686194,0.00018272792,0.0018603673],"genre_scores_gemma":[0.9974572,0.0002166348,0.0012008788,0.00007712655,0.00010520276,0.000019875573,0.00013339355,0.00006490106,0.0007247308],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9993364,0.00014445219,0.00013738188,0.00013582146,0.00016443085,0.000081503575],"domain_scores_gemma":[0.99794,0.0007401941,0.0007904588,0.00011309498,0.000104137514,0.00031211253],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00043475316,0.0032727427,0.0010253902,0.0023360937,0.0014658204,0.0007851607,0.0012199484,0.003080476,0.0033833813],"category_scores_gemma":[0.0019220033,0.0006669184,0.0012951498,0.001152918,0.0022608184,0.00063245924,0.0015651687,0.0016359448,0.0008999719],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0051276544,0.0004101521,0.021733798,0.0003754074,0.00079626124,0.27159587,0.0018673982,0.00265347,0.67668915,0.0049874038,0.0021941646,0.01156929],"study_design_scores_gemma":[0.00061113824,0.001010471,0.135415,0.0002230841,0.001377685,0.52919966,0.0013671125,0.011908172,0.3028327,0.0040879357,0.011632669,0.0003344518],"about_ca_topic_score_codex":0.0020642625,"about_ca_topic_score_gemma":0.0010864043,"teacher_disagreement_score":0.0033833813,"about_ca_system_score_codex":0.0006630891,"about_ca_system_score_gemma":0.0004645001,"threshold_uncertainty_score":0.011318505},"labels":[],"label_agreement":null},{"id":"W1996591375","doi":"10.1038/ng1325","title":"Mutations in VPS33B, encoding a regulator of SNARE-dependent membrane fusion, cause arthrogryposis–renal dysfunction–cholestasis (ARC) syndrome","year":2004,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Cellular transport and secretion","field":"Biochemistry, Genetics and Molecular Biology","cited_by":339,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Hospital for Sick Children","funders":"Wellcome Trust","keywords":"Biology; Genetics; Arthrogryposis; Cholestasis; Endocrinology","score_opus":0.007716541663855614,"score_gpt":0.23166394679207328,"score_spread":0.22394740512821767,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1996591375","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.98921984,0.00097598025,0.005615268,0.0006489847,0.00013515743,0.000054372045,0.00080001686,0.00035145547,0.00219888],"genre_scores_gemma":[0.9960425,0.00034613642,0.0022666024,0.00012215735,0.00004093187,0.000018956323,0.0003891002,0.00007016285,0.0007034767],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99975663,0.000049370192,0.000025755426,0.00004430929,0.00009237845,0.000031537074],"domain_scores_gemma":[0.99940157,0.00015501573,0.00018845122,0.000022885504,0.00002936663,0.00020274552],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00017777784,0.0018964381,0.00045627044,0.0011535579,0.00044467783,0.00030435147,0.00039597056,0.0016516462,0.001961399],"category_scores_gemma":[0.0008169662,0.00038220352,0.0004329597,0.0007731804,0.0010001947,0.000215604,0.0006657591,0.0009805079,0.0008223621],"study_design_candidate":"bench_or_experimental","study_design_consensus":"bench_or_experimental","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0010085013,0.00018330844,0.012592689,0.00017838017,0.00020209169,0.14067253,0.00045108172,0.0015612132,0.8293575,0.0018828333,0.002395508,0.009514281],"study_design_scores_gemma":[0.0010576745,0.00097303966,0.21072477,0.00031752666,0.00069623487,0.5088404,0.0007755504,0.015438281,0.24158052,0.0034123077,0.015945192,0.00023851196],"about_ca_topic_score_codex":0.0024291005,"about_ca_topic_score_gemma":0.001972517,"teacher_disagreement_score":0.0024291005,"about_ca_system_score_codex":0.0003987555,"about_ca_system_score_gemma":0.0002941674,"threshold_uncertainty_score":0.0065615773},"labels":[],"label_agreement":null},{"id":"W1997014674","doi":"10.1038/ng.2772","title":"BMP signaling controls muscle mass","year":2013,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Muscle Physiology and Disorders","field":"Biochemistry, Genetics and Molecular Biology","cited_by":457,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"McGill University","funders":"","keywords":"Myostatin; Biology; Ubiquitin ligase; Muscle atrophy; Muscle hypertrophy; Bone morphogenetic protein; Endocrinology; Internal medicine; Denervation; Signal transduction; Cell biology; Atrophy; Protein degradation; Ubiquitin; Skeletal muscle; Genetics; Gene; Medicine","score_opus":0.004529477471887412,"score_gpt":0.23156383417042997,"score_spread":0.22703435669854255,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1997014674","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.93844146,0.0078707365,0.02219554,0.0018297984,0.00056709244,0.000056295492,0.0016505851,0.00067336735,0.026715208],"genre_scores_gemma":[0.97881806,0.0019392472,0.0041629723,0.0002543802,0.000047727615,0.000031069747,0.00043246878,0.00014020731,0.014173691],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99972326,0.000029259547,0.000016855305,0.00006557294,0.00011189322,0.00005319215],"domain_scores_gemma":[0.9997625,0.000031448446,0.000061901956,0.000029398983,0.00003286792,0.000081954706],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.000214082,0.00044369235,0.00025989066,0.00054485945,0.00027828926,0.0008554551,0.0004138805,0.0007238994,0.0031932418],"category_scores_gemma":[0.0002588049,0.00044797128,0.00021000301,0.00017539636,0.00057220587,0.00039276542,0.00069090055,0.0010464137,0.001142696],"study_design_candidate":"bench_or_experimental","study_design_consensus":"bench_or_experimental","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00011622365,0.00000721033,0.00043137482,0.000017969793,0.0000061187907,0.000060541897,0.000010023143,0.00007005792,0.99459076,0.0015559075,0.00016703963,0.0029667076],"study_design_scores_gemma":[0.000049181286,0.00009193927,0.021599108,0.000032850996,0.000039995426,0.00058419624,0.00009266946,0.0021707986,0.9589558,0.0021034696,0.014264014,0.000015964342],"about_ca_topic_score_codex":0.000633442,"about_ca_topic_score_gemma":0.0011040549,"teacher_disagreement_score":0.0031932418,"about_ca_system_score_codex":0.0006090901,"about_ca_system_score_gemma":0.0002598924,"threshold_uncertainty_score":0.010682404},"labels":[],"label_agreement":null},{"id":"W1997197927","doi":"10.1038/ng1002-229","title":"Top ten biotechnologies for improving health in developing countries","year":2002,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Biotechnology and Related Fields","field":"Medicine","cited_by":351,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Toronto","funders":"Hospital for Sick Children; University of Toronto; University Health Network; GlaxoSmithKline","keywords":"Developing country; Relevance (law); Global health; Biotechnology; Economic growth; Position (finance); Developed country; Biology; Political science; Business; Health care; Environmental health; Medicine; Economics","score_opus":0.012864619243340434,"score_gpt":0.2764220522374364,"score_spread":0.26355743299409595,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1997197927","genre_codex":"commentary","genre_gemma":"review","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"review","genre_consensus":null,"domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.020563899,0.17063361,0.007503373,0.45753002,0.0255936,0.00020960424,0.0020500445,0.0006181481,0.31529775],"genre_scores_gemma":[0.27250254,0.2998754,0.05052791,0.12876204,0.0146726,0.0004534084,0.002076951,0.00023186664,0.23089737],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.9984061,0.0003892356,0.000088255845,0.00010217335,0.0006712873,0.0003429223],"domain_scores_gemma":[0.99739933,0.00045131115,0.00016836432,0.00012991043,0.0005815251,0.0012695518],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0033814972,0.0012662358,0.00082908897,0.0016074622,0.0018562814,0.0066459742,0.00073829165,0.0026532589,0.034618393],"category_scores_gemma":[0.00315019,0.00031216818,0.00045436766,0.0019926652,0.001567329,0.0023084371,0.0017212353,0.003009253,0.0064148596],"study_design_candidate":"not_applicable","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00039968136,0.0002833868,0.003107417,0.0013090377,0.00006479681,0.00030194718,0.0001848396,0.0005601373,0.0037172574,0.07172403,0.45228642,0.46606106],"study_design_scores_gemma":[0.00011185262,0.00018133066,0.0062424834,0.0007915259,0.00007497008,0.00035516126,0.0006716341,0.00038477022,0.0021539105,0.030109797,0.95889676,0.000025814232],"about_ca_topic_score_codex":0.0026653798,"about_ca_topic_score_gemma":0.009670413,"teacher_disagreement_score":0.034618393,"about_ca_system_score_codex":0.0030383607,"about_ca_system_score_gemma":0.010620421,"threshold_uncertainty_score":0.115810096},"labels":[],"label_agreement":null},{"id":"W1997407692","doi":"10.1038/ng.2386","title":"Mutations in ABCD4 cause a new inborn error of vitamin B12 metabolism","year":2012,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Folate and B Vitamins Research","field":"Medicine","cited_by":237,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"McGill University and Génome Québec Innovation Centre; McGill University","funders":"Canadian Institutes of Health Research","keywords":"Biology; Genetics; Vitamin B12; ATP-binding cassette transporter; Gene; Mutation; Transporter; Biochemistry","score_opus":0.030826974068247404,"score_gpt":0.358764254153035,"score_spread":0.32793728008478756,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1997407692","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9713587,0.0019897071,0.0064410847,0.0061871447,0.0023331544,0.00018467034,0.0015062805,0.00047859247,0.009520709],"genre_scores_gemma":[0.9880023,0.0005662259,0.0038295104,0.0009292868,0.00070812815,0.000029108103,0.00036955823,0.00013613497,0.005429775],"study_design_codex":"case_report","study_design_gemma":"observational","domain_scores_codex":[0.9991602,0.00010615493,0.00012209213,0.00021908115,0.0002667007,0.00012581574],"domain_scores_gemma":[0.99799985,0.0009145278,0.00036098494,0.0000931264,0.00023101184,0.00040053952],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00045529357,0.0036232085,0.0013224398,0.0021676228,0.00150193,0.0010885498,0.001420882,0.0059026997,0.004772409],"category_scores_gemma":[0.0029228106,0.00055624684,0.0011995118,0.0012785505,0.0020837956,0.00057873264,0.0010492122,0.0019697186,0.0008848791],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0016098422,0.00034163092,0.023727302,0.00019583464,0.00033993478,0.8714785,0.0005503697,0.0008727392,0.07788994,0.0044290866,0.005114146,0.013450651],"study_design_scores_gemma":[0.0006097165,0.0008505297,0.04516703,0.000106960055,0.00078818866,0.86630315,0.00051412167,0.005377905,0.05284956,0.0048011825,0.022461433,0.00017028375],"about_ca_topic_score_codex":0.0038030471,"about_ca_topic_score_gemma":0.0025178983,"teacher_disagreement_score":0.0059026997,"about_ca_system_score_codex":0.0012890287,"about_ca_system_score_gemma":0.0007739615,"threshold_uncertainty_score":0.015965223},"labels":[],"label_agreement":null},{"id":"W1997751006","doi":"10.1038/ng.3034","title":"Whole-genome sequencing of 234 bulls facilitates mapping of monogenic and complex traits in cattle","year":2014,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Genetic and phenotypic traits in livestock","field":"Biochemistry, Genetics and Molecular Biology","cited_by":904,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Alberta","funders":"Agence Nationale de la Recherche","keywords":"Biology; Genome; Genetics; Whole genome sequencing; 1000 Genomes Project; Coat; Genome-wide association study; Breed; Bovine genome; DNA sequencing; Reference genome; Population; Genomics; Genotype; Single-nucleotide polymorphism; Gene","score_opus":0.015824194134613303,"score_gpt":0.23864286292040676,"score_spread":0.22281866878579346,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1997751006","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9931356,0.00046838875,0.0023752956,0.00003821188,0.000008261677,0.00001535663,0.0027908531,0.00002256945,0.0011455702],"genre_scores_gemma":[0.9854172,0.00043930358,0.0047880425,0.00009755456,0.000017210392,0.000030429626,0.0060859863,0.00006192465,0.00306234],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9996803,0.00006959697,0.000013580854,0.000104004816,0.00006275682,0.00006978971],"domain_scores_gemma":[0.9996278,0.00015505112,0.000051050676,0.00004698673,0.000052725674,0.00006640121],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.000683573,0.00026359948,0.00049368263,0.0009391677,0.00055439404,0.0006205971,0.00039748452,0.00052125484,0.003616259],"category_scores_gemma":[0.00053521217,0.0002619924,0.00038445843,0.0008873313,0.0002820973,0.0001940534,0.0004460757,0.00037865413,0.0006165283],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0012335601,0.00014584036,0.32726696,0.00023269077,0.0008137177,0.001197448,0.0019045301,0.0011707214,0.6020163,0.0009429763,0.0010964633,0.061978802],"study_design_scores_gemma":[0.00003166829,0.000102491824,0.9871803,0.000019203431,0.00024343534,0.00065454503,0.0002777236,0.00035695086,0.0057405075,0.00014902806,0.005231858,0.000012290159],"about_ca_topic_score_codex":0.011207954,"about_ca_topic_score_gemma":0.026164673,"teacher_disagreement_score":0.011207954,"about_ca_system_score_codex":0.000266075,"about_ca_system_score_gemma":0.00028044992,"threshold_uncertainty_score":0.022285461},"labels":[],"label_agreement":null},{"id":"W1998367819","doi":"10.1038/ng.2413","title":"Recurrent somatic TET2 mutations in normal elderly individuals with clonal hematopoiesis","year":2012,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Acute Myeloid Leukemia Research","field":"Medicine","cited_by":808,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Montreal Heart Institute; Université de Montréal; Hôpital Maisonneuve-Rosemont","funders":"National Institute of Diabetes and Digestive and Kidney Diseases; National Cancer Institute; Howard Hughes Medical Institute","keywords":"Biology; Somatic cell; Haematopoiesis; Myeloid; Exome sequencing; Somatic evolution in cancer; Genetics; DNA methylation; Mutation; Exome; Stem cell; Cancer research; Gene","score_opus":0.014817905483908753,"score_gpt":0.3101964165340708,"score_spread":0.29537851105016205,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1998367819","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9990988,0.00013193864,0.00009686587,0.000032559798,0.0000066020984,0.0000029426674,0.000053683307,0.000008367488,0.0005683842],"genre_scores_gemma":[0.99957806,0.000043356555,0.000079059544,0.000023054885,0.000015592414,0.0000011685612,0.000041170468,0.0000035907412,0.00021495819],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99985874,0.000015130341,0.000024737947,0.000033651657,0.000032525913,0.000035114637],"domain_scores_gemma":[0.9996431,0.00010343595,0.00010176282,0.000027296157,0.000050890027,0.00007357371],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00016115147,0.00030587747,0.0002494132,0.000861292,0.0004092732,0.00032088938,0.00025735682,0.0005344498,0.0021600123],"category_scores_gemma":[0.0014824513,0.0001640005,0.0001645905,0.00050585665,0.00027207576,0.0002475612,0.0002973792,0.00022173369,0.00032123405],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0008852631,0.00008274684,0.838453,0.00004850076,0.000064232605,0.10143266,0.0011321991,0.00030307713,0.03561882,0.00031683358,0.0009287685,0.02073396],"study_design_scores_gemma":[0.000034946606,0.0004156257,0.75383973,0.000017706447,0.00014971431,0.23741077,0.0010888296,0.0008779584,0.004209336,0.0004930123,0.0014314635,0.000030954718],"about_ca_topic_score_codex":0.0018677579,"about_ca_topic_score_gemma":0.0022253988,"teacher_disagreement_score":0.0021600123,"about_ca_system_score_codex":0.00017985814,"about_ca_system_score_gemma":0.00015687612,"threshold_uncertainty_score":0.0072259903},"labels":[],"label_agreement":null},{"id":"W1999580244","doi":"10.1038/ng.913","title":"Heritable GATA2 mutations associated with familial myelodysplastic syndrome and acute myeloid leukemia","year":2011,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Acute Myeloid Leukemia Research","field":"Medicine","cited_by":601,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Calgary","funders":"National Institute of Diabetes and Digestive and Kidney Diseases; University of Washington","keywords":"GATA2; Biology; Myeloid leukemia; Transactivation; Missense mutation; Genetics; Myelodysplastic syndromes; Cancer research; Mutation; Zinc finger; Myeloid; Leukemia; Gene; Transcription factor; Bone marrow; Immunology","score_opus":0.015048788931000591,"score_gpt":0.2598435909749958,"score_spread":0.24479480204399523,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1999580244","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99673814,0.00017354083,0.0007643946,0.00016564719,0.000028453393,0.000020115129,0.00017075097,0.00003515405,0.0019038839],"genre_scores_gemma":[0.99899346,0.000047562065,0.00043611476,0.00004485744,0.000038881604,0.0000060792354,0.00007225618,0.000013654938,0.00034717616],"study_design_codex":"case_report","study_design_gemma":"observational","domain_scores_codex":[0.99955124,0.000095769574,0.0000558628,0.00009069633,0.00013777803,0.00006864698],"domain_scores_gemma":[0.9993655,0.0002190986,0.00021241412,0.000031506523,0.000031307398,0.00014017361],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00023138244,0.0010872657,0.00041647544,0.0012747421,0.0005875463,0.00031037457,0.00045896694,0.0010465996,0.0037094548],"category_scores_gemma":[0.0011183039,0.00031515103,0.00039398682,0.00071327045,0.00096620544,0.00023410881,0.00079512584,0.0005598977,0.00035953845],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.001016579,0.0001838805,0.11300611,0.00011089735,0.00028189752,0.55175525,0.0011172083,0.0011297563,0.31781393,0.0040676347,0.0014134303,0.008103352],"study_design_scores_gemma":[0.00031703993,0.00038411125,0.31639895,0.000046088997,0.000385456,0.64380366,0.00053239154,0.0025055658,0.030357825,0.0017822317,0.0034172265,0.00006942235],"about_ca_topic_score_codex":0.0010328463,"about_ca_topic_score_gemma":0.0016309842,"teacher_disagreement_score":0.0037094548,"about_ca_system_score_codex":0.0002835466,"about_ca_system_score_gemma":0.00024069451,"threshold_uncertainty_score":0.012409389},"labels":[],"label_agreement":null},{"id":"W1999674531","doi":"10.1038/ng2093","title":"Challenges and standards in integrating surveys of structural variation","year":2007,"lang":"en","type":"review","venue":"Nature Genetics","topic":"Genomic variations and chromosomal abnormalities","field":"Biochemistry, Genetics and Molecular Biology","cited_by":417,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"SickKids Foundation; MaRS; Hospital for Sick Children","funders":"Wellcome Trust","keywords":"Variation (astronomy); Biology; Structural variation; Data science; Human genetic variation; Computational biology; Copy-number variation; Genetic variation; Genome; Human genome; Genetics; Computer science; Gene","score_opus":0.026693671789386333,"score_gpt":0.32936964745760416,"score_spread":0.30267597566821786,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1999674531","genre_codex":"review","genre_gemma":"review","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"review","genre_consensus":"review","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.000534564,0.9297091,0.027653763,0.032545332,0.004818791,0.000057663987,0.00020547918,0.00022039234,0.0042548925],"genre_scores_gemma":[0.0046051,0.9001615,0.071982734,0.015372806,0.0052687777,0.00020405806,0.00030341503,0.00010554507,0.001995991],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.9877499,0.00420895,0.001240128,0.0018899597,0.0045340583,0.00037703605],"domain_scores_gemma":[0.8823545,0.08958463,0.002031047,0.00448674,0.01940283,0.002140207],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.06561725,0.0016492773,0.0052103144,0.006268384,0.0015647456,0.0073939655,0.008176076,0.007864899,0.0022036342],"category_scores_gemma":[0.07558712,0.001013683,0.0011637044,0.007816092,0.008842551,0.011632681,0.006216633,0.011580539,0.0017736625],"study_design_candidate":"not_applicable","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00006551285,0.000061214014,0.0014787834,0.0070477263,0.00012545886,0.00029618575,0.00067704613,0.001076194,0.0011877873,0.05901698,0.05406615,0.8749009],"study_design_scores_gemma":[0.000027392573,0.00011562834,0.0024506864,0.007023277,0.00014503457,0.0014762831,0.0008885179,0.000705289,0.00090651884,0.07658207,0.90957123,0.00010803112],"about_ca_topic_score_codex":0.006790022,"about_ca_topic_score_gemma":0.008566754,"teacher_disagreement_score":0.06561725,"about_ca_system_score_codex":0.0038536955,"about_ca_system_score_gemma":0.008180289,"threshold_uncertainty_score":0.34702134},"labels":[],"label_agreement":null},{"id":"W1999690368","doi":"10.1038/ng.1017","title":"Meta-analysis of genome-wide association studies identifies three new risk loci for atopic dermatitis","year":2011,"lang":"en","type":"review","venue":"Nature Genetics","topic":"Dermatology and Skin Diseases","field":"Medicine","cited_by":351,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Toronto; Ontario Institute for Cancer Research","funders":"National Institute on Alcohol Abuse and Alcoholism; National Institute on Drug Abuse; Lundbeckfonden; Wellcome Trust","keywords":"Biology; Atopic dermatitis; Genome-wide association study; Genetics; Genetic association; Computational biology; Single-nucleotide polymorphism; Gene; Immunology; Genotype","score_opus":0.10403081684346793,"score_gpt":0.37061377796245404,"score_spread":0.2665829611189861,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1999690368","genre_codex":"review","genre_gemma":"review","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"review","genre_consensus":"review","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.0027704218,0.99549747,0.00091711956,0.00035628205,0.00008556723,0.000006168895,0.00010497013,0.000017254299,0.00024477846],"genre_scores_gemma":[0.03542133,0.9608048,0.0023554536,0.00043644,0.00034120213,0.000016320651,0.0003593329,0.000009107553,0.0002560558],"study_design_codex":"design_other","study_design_gemma":"meta_analysis","domain_scores_codex":[0.99912137,0.00026189449,0.00013188676,0.00024020438,0.00019992783,0.000044680775],"domain_scores_gemma":[0.9969022,0.0023564443,0.0003601999,0.0001100647,0.00020877627,0.00006226506],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.002497197,0.0014685694,0.0040250216,0.002175613,0.00018820596,0.0011856582,0.0013663449,0.0010776807,0.0015564456],"category_scores_gemma":[0.0034528214,0.0004805523,0.0030952208,0.0032521852,0.00030836393,0.00063478516,0.00066073646,0.0010724417,0.00029451202],"study_design_candidate":"meta_analysis","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0016758499,0.000093885305,0.04456861,0.032649737,0.040379908,0.0015736474,0.00011007585,0.0011925574,0.0033080154,0.0011781405,0.009233848,0.8640358],"study_design_scores_gemma":[0.0014776706,0.0012668282,0.34336913,0.02344391,0.31686214,0.02268309,0.000557339,0.0028441262,0.00589503,0.018558161,0.26266766,0.0003748673],"about_ca_topic_score_codex":0.0012508127,"about_ca_topic_score_gemma":0.003772312,"teacher_disagreement_score":0.0040250216,"about_ca_system_score_codex":0.00039592228,"about_ca_system_score_gemma":0.0010254156,"threshold_uncertainty_score":0.013206601},"labels":[],"label_agreement":null},{"id":"W2000197503","doi":"10.1038/ng.3282","title":"Mutations in KCNH1 and ATP6V1B2 cause Zimmermann-Laband syndrome","year":2015,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Advanced biosensing and bioanalysis techniques","field":"Biochemistry, Genetics and Molecular Biology","cited_by":218,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Université de Montréal; Centre Hospitalier Universitaire Sainte-Justine","funders":"Istituto Superiore di Sanità; Ministero della Salute; Deutsche Forschungsgemeinschaft; Ospedale Pediatrico Bambino Gesù","keywords":"Missense mutation; Biology; Mutation; Mutant; Genetics; Protein subunit; Cell biology; Endocrinology; Gene","score_opus":0.012247301184163248,"score_gpt":0.2977956595364011,"score_spread":0.28554835835223785,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2000197503","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.97742575,0.0021353427,0.0070728986,0.0029424974,0.00081923604,0.00015746822,0.0014143997,0.0005073325,0.007525085],"genre_scores_gemma":[0.9940739,0.0004130645,0.0032277436,0.00024851452,0.00021472076,0.000027729442,0.00022584538,0.00008778294,0.0014806302],"study_design_codex":"case_report","study_design_gemma":"observational","domain_scores_codex":[0.99903095,0.00011402045,0.00015437769,0.0002537057,0.0003244775,0.00012251313],"domain_scores_gemma":[0.9977849,0.00084763835,0.0006012106,0.00007412389,0.00009552396,0.0005966321],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00044316272,0.0045385305,0.0009226341,0.002662048,0.0010852112,0.0008711245,0.0018120438,0.0050460915,0.0053119683],"category_scores_gemma":[0.003292884,0.000753583,0.00088294025,0.0018655626,0.002229168,0.0011323921,0.0015135903,0.0016720569,0.0009866299],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0005575477,0.0001076807,0.014191456,0.0001938994,0.00019376962,0.90640295,0.00050967414,0.0006350363,0.066197746,0.0021527929,0.0019178155,0.0069396705],"study_design_scores_gemma":[0.00026647394,0.00029495213,0.042338464,0.00011734815,0.00034428985,0.9078408,0.00048764696,0.0030215776,0.0354955,0.0028073387,0.006827997,0.00015753736],"about_ca_topic_score_codex":0.0026530342,"about_ca_topic_score_gemma":0.0023638434,"teacher_disagreement_score":0.0053119683,"about_ca_system_score_codex":0.0006617012,"about_ca_system_score_gemma":0.00064859755,"threshold_uncertainty_score":0.01777029},"labels":[],"label_agreement":null},{"id":"W2000485285","doi":"10.1038/ng1095","title":"Disruption of Cnp1 uncouples oligodendroglial functions in axonal support and myelination","year":2003,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Neurogenesis and neuroplasticity mechanisms","field":"Neuroscience","cited_by":1043,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"McGill University","funders":"","keywords":"Oligodendrocyte; Myelin; Biology; Neuroscience; Neurodegeneration; Cell biology; Neuroglia; Central nervous system; White matter; Multiple sclerosis; Immunology; Pathology; Medicine","score_opus":0.02016683027708602,"score_gpt":0.2664285069786172,"score_spread":0.24626167670153118,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2000485285","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.979391,0.0016975631,0.011548478,0.00091932714,0.00022065944,0.000063956606,0.0010346925,0.00040820095,0.004716254],"genre_scores_gemma":[0.98565763,0.00072693283,0.005610216,0.0001656663,0.000022379247,0.00006086931,0.00044186047,0.00024126958,0.0070732636],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99957174,0.000036080208,0.000045308654,0.00011089115,0.00014231144,0.00009369585],"domain_scores_gemma":[0.9992994,0.00013785897,0.00022928917,0.000067605586,0.000044144097,0.00022160994],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00034371228,0.0008066377,0.0005457189,0.00084050925,0.00065104576,0.00097343343,0.0012012115,0.0010511911,0.0028226678],"category_scores_gemma":[0.00040338575,0.00062769814,0.00036275917,0.000349079,0.0014396886,0.00072404253,0.0010143535,0.0022711265,0.0008158692],"study_design_candidate":"bench_or_experimental","study_design_consensus":"bench_or_experimental","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00016825438,0.000026563002,0.00010515894,0.000035948065,0.000006863217,0.00020889453,0.000019220523,0.00025460788,0.99682695,0.0011397323,0.000111881025,0.0010959235],"study_design_scores_gemma":[0.00002871041,0.00004168418,0.0015382781,0.000007662475,0.000015118188,0.0004463289,0.000037587044,0.0017925604,0.9935562,0.0002449948,0.0022813617,0.000009454435],"about_ca_topic_score_codex":0.004090923,"about_ca_topic_score_gemma":0.00944374,"teacher_disagreement_score":0.004090923,"about_ca_system_score_codex":0.0019619043,"about_ca_system_score_gemma":0.0012155309,"threshold_uncertainty_score":0.014234662},"labels":[],"label_agreement":null},{"id":"W2001188663","doi":"10.1038/ng.886","title":"Increased exonic de novo mutation rate in individuals with schizophrenia","year":2011,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Genomics and Rare Diseases","field":"Biochemistry, Genetics and Molecular Biology","cited_by":443,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Centre Hospitalier Universitaire Sainte-Justine; Université de Montréal; McGill University; Douglas Mental Health University Institute; Centre Hospitalier de l’Université de Montréal","funders":"Canadian Institutes of Health Research","keywords":"Proband; Genetics; Biology; Schizophrenia (object-oriented programming); Exome sequencing; Psychosis; Heritability; Genetic association; Mutation; Gene; Psychology; Genotype; Single-nucleotide polymorphism; Psychiatry","score_opus":0.006587245054161709,"score_gpt":0.22425801298139214,"score_spread":0.21767076792723042,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2001188663","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9985329,0.00018502478,0.00039154728,0.00005680533,0.00001858468,0.000003908463,0.0002979053,0.00002972079,0.00048361626],"genre_scores_gemma":[0.999143,0.00008186019,0.00029132658,0.000031138818,0.000011875229,0.000003324716,0.00012332755,0.00001735096,0.00029680118],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99945706,0.00012877218,0.000099175086,0.00015490389,0.000102465034,0.000057681398],"domain_scores_gemma":[0.9983504,0.00068377797,0.0004888302,0.00014515316,0.00015054684,0.00018142085],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0004492846,0.00056006206,0.0004973491,0.0023980583,0.00045908813,0.0005718335,0.00034560674,0.0009341064,0.0055916086],"category_scores_gemma":[0.002517041,0.0002880215,0.00041057996,0.0007834156,0.00029660566,0.00038153736,0.00034461738,0.00056249514,0.0005153023],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0030421217,0.00017492993,0.74768645,0.00013728207,0.00048461484,0.01833732,0.00096264144,0.00080638076,0.20676206,0.0007842564,0.0007464637,0.020075534],"study_design_scores_gemma":[0.00004939704,0.00034881817,0.9463222,0.00003193068,0.00032049094,0.03792036,0.00040899927,0.0015040626,0.011438847,0.0008681463,0.0007372821,0.00004930855],"about_ca_topic_score_codex":0.0013741062,"about_ca_topic_score_gemma":0.0010749748,"teacher_disagreement_score":0.0055916086,"about_ca_system_score_codex":0.00016629911,"about_ca_system_score_gemma":0.00017664625,"threshold_uncertainty_score":0.018705785},"labels":[],"label_agreement":null},{"id":"W2001673724","doi":"10.1038/ng821","title":"Mutant chromatin remodeling protein SMARCAL1 causes Schimke immuno-osseous dysplasia","year":2002,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Immunodeficiency and Autoimmune Disorders","field":"Immunology and Microbiology","cited_by":330,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Toronto; Hospital for Sick Children; SickKids Foundation; Alberta Children's Hospital; University of Alberta","funders":"","keywords":"Biology; Genetics; Missense mutation; Frameshift mutation; Primary immunodeficiency; Allele; Chromatin remodeling; Immunodeficiency; Haploinsufficiency; Mutation; Chromatin; Cancer research; Gene; Phenotype","score_opus":0.009331783786774878,"score_gpt":0.2221670775724142,"score_spread":0.2128352937856393,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2001673724","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99141544,0.0008469893,0.003004015,0.00023405346,0.00008595101,0.000050749273,0.0008463611,0.00042947056,0.003087005],"genre_scores_gemma":[0.9969434,0.0002240685,0.00078707846,0.000043031036,0.000027555941,0.000019618887,0.00027296803,0.00006387413,0.0016182564],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9995314,0.000094282754,0.00007097992,0.00010147865,0.00012329822,0.0000785778],"domain_scores_gemma":[0.9992737,0.0002220737,0.00022881628,0.00006976386,0.000030284955,0.0001753216],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0002278742,0.0013900588,0.0005840456,0.0018736449,0.00052664895,0.0004019923,0.0009699058,0.0013284588,0.0049083997],"category_scores_gemma":[0.0004753556,0.0005303745,0.00048791405,0.0006114271,0.0010431206,0.00019353676,0.0006206796,0.00084783917,0.0011313796],"study_design_candidate":"bench_or_experimental","study_design_consensus":"bench_or_experimental","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0008215379,0.00015983229,0.0019142358,0.000113779264,0.00008975326,0.02025929,0.00007387204,0.000588712,0.9716905,0.0010579876,0.00052282034,0.0027077175],"study_design_scores_gemma":[0.0005109358,0.0007570487,0.043955307,0.000048034126,0.00045164546,0.1151288,0.00028288763,0.0062824246,0.8203722,0.0009175495,0.011212301,0.000080775884],"about_ca_topic_score_codex":0.0013172827,"about_ca_topic_score_gemma":0.0013633247,"teacher_disagreement_score":0.0049083997,"about_ca_system_score_codex":0.0004570658,"about_ca_system_score_gemma":0.0003263922,"threshold_uncertainty_score":0.016420305},"labels":[],"label_agreement":null},{"id":"W2001790878","doi":"10.1038/ng.3096","title":"Hotspot activating PRKD1 somatic mutations in polymorphous low-grade adenocarcinomas of the salivary glands","year":2014,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Salivary Gland Tumors Diagnosis and Treatment","field":"Medicine","cited_by":213,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Western University; Princess Margaret Cancer Centre; University of Toronto; Ontario Institute for Cancer Research; University Health Network","funders":"National Cancer Institute; Government of Ontario","keywords":"Biology; Salivary gland; Somatic cell; Minor Salivary Glands; Adenocarcinoma; Cancer research; Germline mutation; Pathology; Genetics; Mutation; Gene; Cancer; Biochemistry; Medicine","score_opus":0.009972862239375494,"score_gpt":0.26073378522314317,"score_spread":0.2507609229837677,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2001790878","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9982514,0.00020036369,0.00022173926,0.00005829793,0.000008575352,0.000007067945,0.00012549708,0.000023250344,0.0011038363],"genre_scores_gemma":[0.99967694,0.000037975304,0.000099365345,0.000009447574,0.0000034929,9.862198e-7,0.00002641647,0.000003910826,0.00014156064],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99979085,0.000022536871,0.000027147144,0.00004421347,0.000072208764,0.000043033808],"domain_scores_gemma":[0.9997191,0.00008025647,0.00010063517,0.000022129814,0.000020989788,0.000056984867],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00013926774,0.00025617052,0.0002374781,0.0008328461,0.00030440223,0.00044851672,0.00030396,0.0004300218,0.0029370987],"category_scores_gemma":[0.00052141683,0.00018405112,0.00025054242,0.000538347,0.0003243734,0.00019259259,0.00032250537,0.00025737597,0.00031979085],"study_design_candidate":"bench_or_experimental","study_design_consensus":"bench_or_experimental","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0025828036,0.00018417659,0.31342217,0.0002040795,0.00014259535,0.081056975,0.0005632848,0.0010902414,0.5651847,0.00088359084,0.0009839595,0.033701386],"study_design_scores_gemma":[0.000116851195,0.0004630784,0.7519571,0.00002742248,0.00023907468,0.16274728,0.00067977724,0.0023468714,0.07774751,0.0006825761,0.0029543035,0.000038247425],"about_ca_topic_score_codex":0.0008606276,"about_ca_topic_score_gemma":0.0017437745,"teacher_disagreement_score":0.0029370987,"about_ca_system_score_codex":0.00029514477,"about_ca_system_score_gemma":0.0001481899,"threshold_uncertainty_score":0.009825587},"labels":[],"label_agreement":null},{"id":"W2002208068","doi":"10.1038/ng.2231","title":"Meta-analysis identifies nine new loci associated with rheumatoid arthritis in the Japanese population","year":2012,"lang":"en","type":"review","venue":"Nature Genetics","topic":"Systemic Lupus Erythematosus Research","field":"Medicine","cited_by":332,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Toronto; University Health Network; Mount Sinai Hospital","funders":"RIKEN","keywords":"Rheumatoid arthritis; Genome-wide association study; Arthritis; Population; Meta-analysis; Medicine; Immunology; Autoimmune disease; Genetic association; Disease; Internal medicine; Biology; Genetics; Single-nucleotide polymorphism; Genotype; Gene","score_opus":0.09627041378390187,"score_gpt":0.36601277706926366,"score_spread":0.2697423632853618,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2002208068","genre_codex":"review","genre_gemma":"review","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"review","genre_consensus":"review","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.011450035,0.98666847,0.0007166287,0.00039099218,0.00012217702,0.000011494748,0.0002980654,0.00001784799,0.00032420483],"genre_scores_gemma":[0.135333,0.85949856,0.002563343,0.00079198787,0.00043882953,0.000035918518,0.0009583649,0.000017484632,0.00036254263],"study_design_codex":"design_other","study_design_gemma":"meta_analysis","domain_scores_codex":[0.99890184,0.00032030643,0.00021979745,0.00030560413,0.00019156418,0.00006081006],"domain_scores_gemma":[0.99770075,0.0014726488,0.00039138334,0.00012685507,0.00023494862,0.000073493175],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0024746128,0.0016832615,0.004085778,0.0029744245,0.00035620507,0.0013131747,0.0014134995,0.0010073627,0.0015646301],"category_scores_gemma":[0.0034806065,0.00056503405,0.005240999,0.004529984,0.0003753221,0.0005647213,0.000795457,0.00082526304,0.00016089814],"study_design_candidate":"meta_analysis","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0038310322,0.00015731658,0.18868415,0.07095067,0.1964309,0.0029222565,0.00040225752,0.0016024124,0.0053317486,0.00094293954,0.008468087,0.52027637],"study_design_scores_gemma":[0.0008899089,0.000791361,0.3647772,0.008615489,0.56594497,0.0058590043,0.00040722545,0.0008729978,0.0019270645,0.0031864378,0.046538223,0.00019018808],"about_ca_topic_score_codex":0.004483472,"about_ca_topic_score_gemma":0.010266615,"teacher_disagreement_score":0.004483472,"about_ca_system_score_codex":0.0005743527,"about_ca_system_score_gemma":0.0014310362,"threshold_uncertainty_score":0.013087153},"labels":[],"label_agreement":null},{"id":"W2002424665","doi":"10.1038/ng1958","title":"Interleukin-2 gene variation impairs regulatory T cell function and causes autoimmunity","year":2007,"lang":"en","type":"article","venue":"Nature Genetics","topic":"T-cell and B-cell Immunology","field":"Immunology and Microbiology","cited_by":362,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Institute of Infection and Immunity; University of Calgary","funders":"Wellcome Trust","keywords":"Biology; Immune system; Autoimmunity; Regulatory T cell; IL-2 receptor; Allele; T cell; Gene; Autoimmune disease; Immunology; Genetics; Cytokine; Homeostasis; Interleukin 2; Cell biology; Antibody","score_opus":0.006191305024200562,"score_gpt":0.21431116948203238,"score_spread":0.20811986445783182,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2002424665","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9967038,0.0001802035,0.001507288,0.00014678073,0.000058284597,0.0000123944965,0.0002752123,0.00018027103,0.0009357067],"genre_scores_gemma":[0.9973974,0.00017577501,0.0009990283,0.00008508051,0.00003584591,0.000016836504,0.00017626418,0.00013348379,0.0009803083],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.99945897,0.0001801656,0.00005440092,0.00011356392,0.000103416314,0.00008942726],"domain_scores_gemma":[0.999326,0.00024710142,0.00018328863,0.000070940296,0.000018464665,0.00015420503],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00023753401,0.0009189397,0.00038305233,0.0008254247,0.0002468346,0.00041819568,0.0004800459,0.00079092797,0.003800212],"category_scores_gemma":[0.00040435715,0.00037843978,0.00034615787,0.0004383994,0.0006619712,0.00015613086,0.0003738211,0.0013313029,0.00039902536],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0004825646,0.00009765769,0.0006623558,0.000018771176,0.000024564268,0.0004064572,0.000018102039,0.00015753017,0.99689037,0.00021506025,0.00008396034,0.0009425531],"study_design_scores_gemma":[0.00083106424,0.0012917916,0.043010224,0.000023573162,0.00034576943,0.007479593,0.00013304828,0.0043304665,0.93768346,0.00093549985,0.0038653992,0.000070119735],"about_ca_topic_score_codex":0.00045117296,"about_ca_topic_score_gemma":0.00072528835,"teacher_disagreement_score":0.003800212,"about_ca_system_score_codex":0.00026872073,"about_ca_system_score_gemma":0.00025120977,"threshold_uncertainty_score":0.0127129555},"labels":[],"label_agreement":null},{"id":"W2002715948","doi":"10.1038/ng.3242","title":"Genome-wide association analysis of more than 120,000 individuals identifies 15 new susceptibility loci for breast cancer","year":2015,"lang":"en","type":"review","venue":"Nature Genetics","topic":"BRCA gene mutations in cancer","field":"Biochemistry, Genetics and Molecular Biology","cited_by":634,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"McGill University and Génome Québec Innovation Centre; Centre hospitalier universitaire de Québec; Université de Montréal; Sante Montreal; Royal Victoria Hospital; University Health Network; Lunenfeld-Tanenbaum Research Institute; Mount Sinai Hospital; McGill University Health Centre","funders":"National Institute of Environmental Health Sciences; Medical Research Council; Ministero dello Sviluppo Economico; World Health Organization; European Commission; National Cancer Institute; National Institutes of Health; Cancer Research UK; Canadian Institutes of Health Research; National Institute for Health and Care Research; Ministère du Développement Économique, de l’Innovation et de l’Exportation; Francis Crick Institute","keywords":"Biology; Genome-wide association study; Breast cancer; Genetics; Genetic association; Genome; Computational biology; Cancer; Single-nucleotide polymorphism; Gene; Genotype","score_opus":0.02279873656505228,"score_gpt":0.35236563339853283,"score_spread":0.32956689683348056,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2002715948","genre_codex":"review","genre_gemma":"review","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"review","genre_consensus":"review","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.00015350495,0.998295,0.0002417488,0.0005054666,0.0001965625,0.0000043361424,0.000055408538,0.000012083521,0.00053587893],"genre_scores_gemma":[0.0008042815,0.99770576,0.00030137436,0.00048597492,0.0001966688,0.0000057241114,0.00009162143,0.000002070364,0.00040665604],"study_design_codex":"design_other","study_design_gemma":"observational","domain_scores_codex":[0.9997168,0.000042572356,0.00003744492,0.00005985702,0.00011528382,0.000028063172],"domain_scores_gemma":[0.9992969,0.0003584721,0.000082472376,0.000021957876,0.00016839645,0.000071764574],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0011841824,0.0010595476,0.0018365652,0.001879674,0.00023621079,0.0008602352,0.0011805474,0.0013292303,0.0024680698],"category_scores_gemma":[0.0014051227,0.00031301187,0.0005988303,0.0018541815,0.0005211507,0.00077937124,0.000803185,0.0016756895,0.001362877],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00012664765,0.000045677105,0.00087942503,0.008499438,0.00022634343,0.0002492543,0.00002990086,0.00022718076,0.0014884741,0.0018658726,0.043046847,0.943315],"study_design_scores_gemma":[0.00006640168,0.000095404546,0.0038986858,0.0033259594,0.0005696694,0.0014912955,0.000058084785,0.000105728366,0.0006428321,0.0026045563,0.9871044,0.000036921992],"about_ca_topic_score_codex":0.0015827805,"about_ca_topic_score_gemma":0.003882619,"teacher_disagreement_score":0.0024680698,"about_ca_system_score_codex":0.00058101304,"about_ca_system_score_gemma":0.0014011892,"threshold_uncertainty_score":0.008256555},"labels":[],"label_agreement":null},{"id":"W2002871809","doi":"10.1038/ng1440","title":"Implications of correlations between skin color and genetic ancestry for biomedical research","year":2004,"lang":"en","type":"article","venue":"Nature Genetics","topic":"melanin and skin pigmentation","field":"Biochemistry, Genetics and Molecular Biology","cited_by":225,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Toronto","funders":"National Institute of Diabetes and Digestive and Kidney Diseases; National Institutes of Health; National Center for Research Resources; Natural Sciences and Engineering Research Council of Canada; U.S. Department of Defense","keywords":"Genetic genealogy; Biology; Genetic admixture; Skin color; Population; Skin colour; Race (biology); Demography; Genetic variation; Ancestry-informative marker; Evolutionary biology; Proxy (statistics); Genetics; Genotype; Allele frequency; Gene","score_opus":0.03922847006266457,"score_gpt":0.38877603754457857,"score_spread":0.349547567481914,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2002871809","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.83540875,0.01795178,0.059024177,0.05234926,0.0007560857,0.00016804475,0.0015012966,0.000126971,0.032713573],"genre_scores_gemma":[0.9828408,0.0033154364,0.010320612,0.0018342426,0.0004900233,0.00005914179,0.00016693445,0.000027870792,0.0009450619],"study_design_codex":"observational","study_design_gemma":"theoretical_or_conceptual","domain_scores_codex":[0.99155396,0.0066467985,0.00027034112,0.0008087101,0.0004968897,0.00022323453],"domain_scores_gemma":[0.9534141,0.037928056,0.0031570562,0.0030506232,0.0015084939,0.00094183325],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.013215265,0.0006756378,0.00071610574,0.001373172,0.0009113307,0.0018904886,0.0010585246,0.0014448954,0.004207311],"category_scores_gemma":[0.053342164,0.0004096188,0.00047561375,0.0020458456,0.004616833,0.0020337715,0.0011377876,0.0019137958,0.00030708834],"study_design_candidate":"theoretical_or_conceptual","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0014640529,0.0002949278,0.78607565,0.00032293395,0.001429006,0.0019136552,0.0018159571,0.0052502356,0.007827989,0.10496352,0.002334964,0.086307004],"study_design_scores_gemma":[0.00017825,0.00031754174,0.54587156,0.00016913124,0.00066599064,0.0014615238,0.002259074,0.008602264,0.0030909786,0.43095574,0.006330732,0.000097252545],"about_ca_topic_score_codex":0.0028452885,"about_ca_topic_score_gemma":0.002932522,"teacher_disagreement_score":0.013215265,"about_ca_system_score_codex":0.0008263568,"about_ca_system_score_gemma":0.0013436441,"threshold_uncertainty_score":0.069889784},"labels":[],"label_agreement":null},{"id":"W2003422441","doi":"10.1038/ng.2936","title":"Genomic analysis of diffuse intrinsic pontine gliomas identifies three molecular subgroups and recurrent activating ACVR1 mutations","year":2014,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Glioma Diagnosis and Treatment","field":"Medicine","cited_by":654,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"London Health Sciences Centre; McMaster Children's Hospital; Children's Hospital of Eastern Ontario; University of Calgary; BC Children's Hospital; University of Toronto; SickKids Foundation; Hospital for Sick Children; McGill University and Génome Québec Innovation Centre","funders":"National Center for Advancing Translational Sciences; National Cancer Institute; Canadian Institutes of Health Research","keywords":"Biology; Epigenetics; Histone; Cancer; Disease; Cancer research; Gene; Genetics; Bioinformatics; Oncology; Medicine; Internal medicine","score_opus":0.008544328530196873,"score_gpt":0.26473487839458676,"score_spread":0.2561905498643899,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2003422441","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99848205,0.000120017496,0.0002813439,0.0000560198,0.0000019509189,0.000007566078,0.00018691135,0.000017081651,0.0008470935],"genre_scores_gemma":[0.99933356,0.000052182088,0.00024587102,0.00001281464,0.0000029951836,0.000002966438,0.0002076966,0.000006855344,0.00013512846],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9996455,0.000026161073,0.000027461292,0.00011304608,0.00008973333,0.00009821426],"domain_scores_gemma":[0.9996587,0.00009405854,0.00010009215,0.000042654978,0.0000358313,0.00006861725],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00021932281,0.00047781284,0.00034398356,0.001122306,0.00038712152,0.0006259078,0.00047925726,0.0006223942,0.0015695079],"category_scores_gemma":[0.0007537452,0.00015987153,0.0003514974,0.00069963816,0.00053064304,0.00025190724,0.0005188198,0.00033167872,0.00024682895],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0020826948,0.00013604137,0.4216806,0.00010780588,0.00019857184,0.013079083,0.0013208444,0.0010651308,0.51416725,0.0012002753,0.00054850715,0.044413168],"study_design_scores_gemma":[0.000083174906,0.0007783917,0.89902836,0.000021656744,0.00028525316,0.051204998,0.0013052694,0.0022718478,0.040886234,0.0015895403,0.0025095541,0.000035701578],"about_ca_topic_score_codex":0.0029075602,"about_ca_topic_score_gemma":0.0036901382,"teacher_disagreement_score":0.0029075602,"about_ca_system_score_codex":0.00043700123,"about_ca_system_score_gemma":0.00033026637,"threshold_uncertainty_score":0.005781293},"labels":[],"label_agreement":null},{"id":"W2004429375","doi":"10.1038/ng.2560","title":"Identification of 23 new prostate cancer susceptibility loci using the iCOGS custom genotyping array","year":2013,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Epigenetics and DNA Methylation","field":"Biochemistry, Genetics and Molecular Biology","cited_by":550,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"McGill University and Génome Québec Innovation Centre","funders":"National Center for Advancing Translational Sciences; National Institute of General Medical Sciences; National Cancer Institute; Cancer Research UK; Prostate Cancer UK; National Institutes of Health; China Scholarship Council; National Institute for Health and Care Research","keywords":"Biology; Genotyping; Identification (biology); Prostate cancer; Genetics; Computational biology; Cancer; Genotype; Gene","score_opus":0.011992366474070978,"score_gpt":0.2913740822917329,"score_spread":0.2793817158176619,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2004429375","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9439639,0.002451036,0.023992429,0.00068298675,0.0001902917,0.00029862093,0.018450007,0.0014134004,0.008557249],"genre_scores_gemma":[0.92767626,0.0012098697,0.046429988,0.00084524974,0.0001269597,0.000403968,0.014090137,0.00028576204,0.008931777],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9989938,0.000089405854,0.00004926877,0.0004144012,0.00027217792,0.00018090075],"domain_scores_gemma":[0.9992847,0.00019129286,0.00017776141,0.000121454985,0.000089065215,0.00013580122],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0006047468,0.00073403266,0.00083441695,0.0017752184,0.0005181111,0.00089154457,0.000857875,0.00073480007,0.0044707456],"category_scores_gemma":[0.0011830154,0.00068528,0.0008967261,0.0015134938,0.0002903136,0.00022018586,0.000677466,0.00090274727,0.0009130599],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0022451018,0.00031885132,0.19752426,0.0003647456,0.0007961669,0.0016834995,0.0004223002,0.0026858961,0.6087399,0.0014944376,0.009036731,0.17468818],"study_design_scores_gemma":[0.00058216316,0.0008658667,0.64027214,0.00008471967,0.0016728509,0.0055990093,0.00016395637,0.0068984446,0.28823662,0.0021414044,0.053224113,0.0002587408],"about_ca_topic_score_codex":0.005132375,"about_ca_topic_score_gemma":0.01629475,"teacher_disagreement_score":0.005132375,"about_ca_system_score_codex":0.00077633443,"about_ca_system_score_gemma":0.0008007399,"threshold_uncertainty_score":0.014956117},"labels":[],"label_agreement":null},{"id":"W2004430949","doi":"10.1038/87096","title":"Analysis of gene expression patterns in breast cancer by microarray technology","year":2001,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Gene expression and cancer classification","field":"Biochemistry, Genetics and Molecular Biology","cited_by":2,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Ontario Institute for Cancer Research; Lunenfeld-Tanenbaum Research Institute; Mount Sinai Hospital","funders":"","keywords":"Biology; Breast cancer; DNA microarray; Gene expression; Complementary DNA; Microarray; Gene; Computational biology; Gene expression profiling; Cancer; Gene chip analysis; SKBR3; Microarray analysis techniques; Genetics; Cancer research; Bioinformatics","score_opus":0.004580909944999092,"score_gpt":0.2611629540076814,"score_spread":0.2565820440626823,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2004430949","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.950102,0.0068673496,0.031820815,0.0008043218,0.00013585032,0.000101464146,0.00470821,0.00029256765,0.0051675774],"genre_scores_gemma":[0.94823444,0.0060106744,0.03384901,0.00036331927,0.000118639546,0.00033053037,0.0054252665,0.000052770338,0.0056153275],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9997687,0.000039610055,0.000014284432,0.000043602486,0.00007383848,0.00005992427],"domain_scores_gemma":[0.9998336,0.00007765731,0.000022997503,0.000015707334,0.000032853677,0.000017090488],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0002538682,0.00017977225,0.00048031603,0.00072007254,0.00031027163,0.00051309133,0.00019952681,0.00033670315,0.0009969847],"category_scores_gemma":[0.0003621947,0.00019364826,0.00025898239,0.0011830257,0.00021317578,0.00026861829,0.00013134792,0.0006582089,0.0005464405],"study_design_candidate":"bench_or_experimental","study_design_consensus":"bench_or_experimental","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00016582655,0.00002706151,0.0017315963,0.00004987656,0.000011032611,0.00002275077,0.000028213197,0.00007514384,0.9922206,0.00016870351,0.00013704895,0.005362205],"study_design_scores_gemma":[0.000033707765,0.00041052958,0.17589968,0.000020454818,0.00010567773,0.00072944135,0.0002615574,0.0043619517,0.80876327,0.00095399463,0.008435502,0.000024174087],"about_ca_topic_score_codex":0.00089713844,"about_ca_topic_score_gemma":0.001453867,"teacher_disagreement_score":0.0009969847,"about_ca_system_score_codex":0.00033289136,"about_ca_system_score_gemma":0.00022921759,"threshold_uncertainty_score":0.0033352375},"labels":[],"label_agreement":null},{"id":"W2005114144","doi":"10.1038/ng.1020","title":"Genome-wide association study identifies five loci associated with susceptibility to pancreatic cancer in Chinese populations","year":2011,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Epigenetics and DNA Methylation","field":"Biochemistry, Genetics and Molecular Biology","cited_by":196,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Pancreas Centre (Canada)","funders":"National Natural Science Foundation of China","keywords":"Pancreatic cancer; Biology; Single-nucleotide polymorphism; Cancer; Genetics; Genome-wide association study; Gene; Genetic predisposition; Internal medicine; Bioinformatics; Oncology; Genotype; Medicine","score_opus":0.014058841367077912,"score_gpt":0.28994393737222907,"score_spread":0.27588509600515115,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2005114144","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9992009,0.000154966,0.00016674394,0.000049913528,0.0000056735526,0.0000050839453,0.00007744439,0.000005233774,0.0003340113],"genre_scores_gemma":[0.99951637,0.00006962931,0.00010307506,0.000017089795,0.0000065047416,0.0000037672414,0.000063666426,0.000002564717,0.00021734778],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9995247,0.000107859785,0.000048380145,0.00015798713,0.00007347371,0.0000876073],"domain_scores_gemma":[0.99924624,0.00021640414,0.00017008223,0.00007882907,0.00007775474,0.00021067006],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00083284255,0.00056474225,0.00047801013,0.0018303442,0.0011310632,0.0005435901,0.0005758069,0.00045051565,0.002098891],"category_scores_gemma":[0.0009881712,0.00040209232,0.0008324276,0.0023066085,0.0007692497,0.00022613815,0.0005794598,0.00053481007,0.00014190761],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0017011769,0.0001490791,0.96158963,0.000053175212,0.0008060324,0.0015444498,0.0013760026,0.000155067,0.027336823,0.00031626635,0.00019006545,0.0047821724],"study_design_scores_gemma":[0.00004070269,0.00008251517,0.9978036,0.000004162513,0.00029635555,0.00036429,0.00023303111,0.00020704544,0.00070817606,0.00011200047,0.00014093026,0.000007216396],"about_ca_topic_score_codex":0.018209975,"about_ca_topic_score_gemma":0.018099502,"teacher_disagreement_score":0.018209975,"about_ca_system_score_codex":0.0004578374,"about_ca_system_score_gemma":0.0006889589,"threshold_uncertainty_score":0.036207914},"labels":[],"label_agreement":null},{"id":"W2005317228","doi":"10.1038/ng0806-862","title":"From worm genetic networks to complex human diseases","year":2006,"lang":"en","type":"letter","venue":"Nature Genetics","topic":"Genetics, Aging, and Longevity in Model Organisms","field":"Biochemistry, Genetics and Molecular Biology","cited_by":12,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Toronto; McGill University","funders":"","keywords":"Biology; Computational biology; Evolutionary biology; Genetics","score_opus":0.009083873855226169,"score_gpt":0.24646335646112802,"score_spread":0.23737948260590186,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2005317228","genre_codex":"commentary","genre_gemma":"commentary","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"commentary","genre_consensus":"commentary","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.004314985,0.024574595,0.006599683,0.92606795,0.031161983,0.000015466938,0.0001350664,0.00023305733,0.0068972902],"genre_scores_gemma":[0.12912096,0.06859552,0.005711413,0.6410233,0.12702955,0.00017826639,0.0001502123,0.0001568662,0.028033897],"study_design_codex":"not_applicable","study_design_gemma":"theoretical_or_conceptual","domain_scores_codex":[0.99953246,0.00020170686,0.000026712149,0.000057068308,0.00014271942,0.00003934239],"domain_scores_gemma":[0.9950896,0.004004549,0.00016684073,0.00021875741,0.00030471492,0.00021563633],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0014216771,0.0005568757,0.000887265,0.0005653686,0.0008764911,0.0018097563,0.0007325295,0.006620452,0.0047698747],"category_scores_gemma":[0.007695461,0.00033096326,0.0003551671,0.00037615062,0.0024749471,0.0024839137,0.0007919061,0.00880546,0.002167332],"study_design_candidate":"theoretical_or_conceptual","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00042974498,0.000043794626,0.0007402568,0.00033947293,0.00007922918,0.002124324,0.00016162566,0.0011098972,0.0016600231,0.07246424,0.8260546,0.09479291],"study_design_scores_gemma":[0.0006679118,0.00010420583,0.0015869881,0.00026034247,0.00009435172,0.005661741,0.00029707357,0.004755013,0.0023806489,0.35086206,0.6332459,0.0000837592],"about_ca_topic_score_codex":0.0005055243,"about_ca_topic_score_gemma":0.0010479495,"teacher_disagreement_score":0.006620452,"about_ca_system_score_codex":0.00091882807,"about_ca_system_score_gemma":0.0003970405,"threshold_uncertainty_score":0.01595676},"labels":[],"label_agreement":null},{"id":"W2005898133","doi":"10.1038/ng.707","title":"Fine-mapping at three loci known to affect fetal hemoglobin levels explains additional genetic variation","year":2010,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Hemoglobinopathies and Related Disorders","field":"Medicine","cited_by":274,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Université de Montréal; Montreal Heart Institute","funders":"National Heart, Lung, and Blood Institute; Howard Hughes Medical Institute","keywords":"Fetal hemoglobin; Biology; Genotyping; Genetics; Single-nucleotide polymorphism; Missense mutation; MYB; Genetic variation; Globin; Genotype; Hemoglobin; Allele; Fetus; Gene; Mutation; Gene expression; Pregnancy","score_opus":0.01053265286378587,"score_gpt":0.25032360767604733,"score_spread":0.23979095481226145,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2005898133","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9823171,0.0003504749,0.013008857,0.00033460907,0.00007213295,0.000043003558,0.00072378095,0.00018601533,0.0029640342],"genre_scores_gemma":[0.9926178,0.00016964244,0.005658702,0.00024609073,0.00003641099,0.000023771394,0.00034808353,0.00007751952,0.0008219747],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.99949276,0.000086719236,0.000043695716,0.0002043629,0.000105286934,0.00006707818],"domain_scores_gemma":[0.9982114,0.0012197625,0.00019477135,0.00020424441,0.000056981902,0.00011279824],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0006771404,0.0010146498,0.0006640469,0.0014833474,0.00047159966,0.0004748047,0.00094226317,0.0013366389,0.007314599],"category_scores_gemma":[0.0012310804,0.0002789978,0.0012397321,0.0007776383,0.0007127438,0.00022172039,0.00053823466,0.0013006348,0.0004207252],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.001266333,0.00044582062,0.039757546,0.00009190685,0.00040579637,0.0069938586,0.0004160571,0.0011662191,0.9274783,0.002781103,0.00051652244,0.01868068],"study_design_scores_gemma":[0.0007516316,0.00071559165,0.68792003,0.00010463289,0.0015794147,0.028315226,0.00033475307,0.008013185,0.25858712,0.0058136126,0.0077215647,0.00014331467],"about_ca_topic_score_codex":0.0016979688,"about_ca_topic_score_gemma":0.0025699157,"teacher_disagreement_score":0.007314599,"about_ca_system_score_codex":0.0003037514,"about_ca_system_score_gemma":0.00026167012,"threshold_uncertainty_score":0.024469733},"labels":[],"label_agreement":null},{"id":"W2005989052","doi":"10.1038/ng.282","title":"A transcriptome atlas of rice cell types uncovers cellular, functional and developmental hierarchies","year":2009,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Gene expression and cancer classification","field":"Biochemistry, Genetics and Molecular Biology","cited_by":245,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Alberta","funders":"","keywords":"Biology; Transcriptome; Laser capture microdissection; Cell type; Gene expression profiling; Gene; Genetics; Computational biology; Gene expression; Oryza sativa; Cell; Cell biology","score_opus":0.006843994587758041,"score_gpt":0.2203817493830641,"score_spread":0.21353775479530607,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2005989052","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9346369,0.0015315686,0.03048099,0.00019133619,0.00003262114,0.000037733145,0.026318511,0.0011495828,0.005620729],"genre_scores_gemma":[0.9131114,0.0020828287,0.04134137,0.00019150705,0.000033223823,0.00009461698,0.035841573,0.00038808092,0.006915491],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9999137,0.0000051440393,0.0000041436447,0.00003878659,0.000016487287,0.00002175438],"domain_scores_gemma":[0.9998472,0.000027370344,0.000027897535,0.000026938555,0.0000349396,0.000035627396],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00013173361,0.00023995712,0.00034191966,0.0008945428,0.00032032147,0.00047262528,0.00016308764,0.00015514856,0.00096188346],"category_scores_gemma":[0.00012651052,0.00019154542,0.00033020877,0.0012500838,0.00018357651,0.0002710528,0.00028159397,0.00033581466,0.00054682477],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00011504483,0.000008703801,0.0077162283,0.000059083486,0.000021921916,0.000060398033,0.00008202289,0.00035129482,0.98046744,0.00043315272,0.0005342783,0.010150367],"study_design_scores_gemma":[0.00003157617,0.00021353581,0.7413722,0.00002722379,0.00025309878,0.0013708997,0.00037765884,0.009427143,0.21156543,0.0029279238,0.032378774,0.00005456581],"about_ca_topic_score_codex":0.0031543674,"about_ca_topic_score_gemma":0.0069661834,"teacher_disagreement_score":0.0031543674,"about_ca_system_score_codex":0.00036212493,"about_ca_system_score_gemma":0.0005152055,"threshold_uncertainty_score":0.006272018},"labels":[],"label_agreement":null},{"id":"W2006085234","doi":"10.1038/ng.555","title":"Discovery of common Asian copy number variants using integrated high-resolution array CGH and massively parallel DNA sequencing","year":2010,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Genomic variations and chromosomal abnormalities","field":"Biochemistry, Genetics and Molecular Biology","cited_by":200,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Hospital for Sick Children; University of Toronto","funders":"National Human Genome Research Institute; Ministry of Education, Science and Technology; Wellcome Trust; National Institutes of Health; Brigham and Women's Hospital","keywords":"Copy-number variation; Biology; Comparative genomic hybridization; Genetics; Genome; DNA sequencing; Human genome; Copy number analysis; Computational biology; Whole genome sequencing; Genomics; Human genetics; Gene","score_opus":0.007449717051776405,"score_gpt":0.23771278397434253,"score_spread":0.23026306692256612,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2006085234","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9790414,0.0004257927,0.01725191,0.00014324223,0.000029415525,0.000050812432,0.0016012533,0.00016375212,0.0012923985],"genre_scores_gemma":[0.9778488,0.0002271637,0.019528868,0.00008772286,0.000017810238,0.000028753933,0.0012990416,0.000053737098,0.00090808485],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9996735,0.000037561724,0.00003157809,0.00012686031,0.000089636975,0.000040947554],"domain_scores_gemma":[0.99974984,0.00007769309,0.000052235893,0.000047079895,0.000034670833,0.000038525075],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0005021215,0.00033950678,0.00047308952,0.000980394,0.0002517812,0.0007891727,0.00042352648,0.00032425218,0.0011884946],"category_scores_gemma":[0.000696438,0.00023461583,0.00061382074,0.0012222059,0.00024301659,0.00022468762,0.00036446672,0.0005700334,0.0002204436],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0013240963,0.00009590596,0.1344573,0.000104175255,0.0007248468,0.0020609803,0.00036107568,0.0014938158,0.8013276,0.0013385653,0.00050963555,0.05620205],"study_design_scores_gemma":[0.00023618461,0.0006093007,0.66683716,0.000028512717,0.0017797344,0.009805408,0.00044652168,0.02355772,0.28512844,0.0024631277,0.0089968555,0.00011095687],"about_ca_topic_score_codex":0.0034680367,"about_ca_topic_score_gemma":0.005666678,"teacher_disagreement_score":0.0034680367,"about_ca_system_score_codex":0.00028475674,"about_ca_system_score_gemma":0.0002507771,"threshold_uncertainty_score":0.006895721},"labels":[],"label_agreement":null},{"id":"W2007288779","doi":"10.1038/ng0607-698","title":"Reply to “DNA double-strand breaks are not sufficient to initiate recruitment of TRF2”","year":2007,"lang":"en","type":"article","venue":"Nature Genetics","topic":"DNA Repair Mechanisms","field":"Biochemistry, Genetics and Molecular Biology","cited_by":2,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"SickKids Foundation; University of Toronto","funders":"","keywords":"Biology; Genetics; DNA; Double strand; Computational biology; Cell biology; DNA damage","score_opus":0.028337881594557926,"score_gpt":0.3080114887488951,"score_spread":0.2796736071543372,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2007288779","genre_codex":"commentary","genre_gemma":"commentary","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"commentary","genre_consensus":"commentary","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.0009390792,0.0027100244,0.00051346584,0.9138849,0.08094833,0.000019773306,0.00021732484,0.00011068018,0.00065640814],"genre_scores_gemma":[0.0070658894,0.0029020582,0.0008542082,0.9193691,0.061210886,0.00010143194,0.00025072656,0.00006583775,0.008179759],"study_design_codex":"not_applicable","study_design_gemma":"not_applicable","domain_scores_codex":[0.99803346,0.00028040604,0.00032364475,0.00037715165,0.00056764926,0.00041775117],"domain_scores_gemma":[0.9922655,0.003263306,0.0006467668,0.00035810063,0.0021905163,0.0012757068],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0036787167,0.0013867717,0.0018816825,0.0008257945,0.0031317153,0.0028063513,0.0026912072,0.02816079,0.006716487],"category_scores_gemma":[0.0142118875,0.0013966718,0.0016131788,0.000746952,0.0027979387,0.0031089892,0.0028305976,0.043858565,0.0068716034],"study_design_candidate":"not_applicable","study_design_consensus":"not_applicable","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0002509992,0.000061445455,0.00056927593,0.00015920952,0.000055251596,0.0007149018,0.00013821141,0.00012193323,0.002010325,0.0011198355,0.9892006,0.005597993],"study_design_scores_gemma":[0.00027816402,0.00017304326,0.0040717674,0.00017986824,0.00016678474,0.0015777209,0.00065180747,0.0007381626,0.0048122494,0.0049515376,0.9822057,0.00019318219],"about_ca_topic_score_codex":0.0021870306,"about_ca_topic_score_gemma":0.0026754732,"teacher_disagreement_score":0.02816079,"about_ca_system_score_codex":0.0026930817,"about_ca_system_score_gemma":0.0028429015,"threshold_uncertainty_score":0.022468925},"labels":[],"label_agreement":null},{"id":"W2007771322","doi":"10.1038/ng.375","title":"The transcriptional network that controls growth arrest and differentiation in a human myeloid leukemia cell line","year":2009,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Genomics and Chromatin Dynamics","field":"Biochemistry, Genetics and Molecular Biology","cited_by":430,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"McGill University","funders":"U.S. National Library of Medicine; Medical Research Council; National Heart, Lung, and Blood Institute; Schweizerischer Nationalfonds zur Förderung der Wissenschaftlichen Forschung; Ministry of Education, Culture, Sports, Science and Technology; RIKEN; National Health and Medical Research Council; Wellcome Trust","keywords":"Biology; Transcription factor; Gene knockdown; Cellular differentiation; Gene regulatory network; Transcription (linguistics); Transcriptional regulation; Cell biology; Myeloid leukemia; Regulation of gene expression; Computational biology; Cell culture; Gene; Genetics; Gene expression; Cancer research","score_opus":0.003938502606471444,"score_gpt":0.20716260068944997,"score_spread":0.20322409808297853,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2007771322","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9944318,0.0004210042,0.0024031475,0.00012472706,0.0000090569365,0.000010390614,0.0007522488,0.00008016517,0.0017674906],"genre_scores_gemma":[0.99638027,0.0001722717,0.00085972296,0.000031169497,0.0000052057676,0.000010472545,0.0008167149,0.000017554277,0.0017065458],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99993825,0.000006767574,0.0000034200011,0.000017917373,0.000019058834,0.000014496472],"domain_scores_gemma":[0.9999312,0.000013939016,0.0000144228015,0.000011869373,0.000010373831,0.00001814405],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.000059201375,0.00011636533,0.00012788935,0.0002155076,0.00019923404,0.00026634985,0.00012523202,0.00012054638,0.0007403073],"category_scores_gemma":[0.000111903246,0.0001365924,0.000111854926,0.0001906584,0.00014223588,0.00013824816,0.00010453531,0.00024203109,0.0003597116],"study_design_candidate":"bench_or_experimental","study_design_consensus":"bench_or_experimental","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.000058873815,0.000006189232,0.00048611037,0.000004440616,0.0000016155404,0.000021828733,0.000008980426,0.00014653239,0.99839836,0.00024921887,0.000035411533,0.000582373],"study_design_scores_gemma":[0.000024273693,0.00012304683,0.035531323,0.000004668761,0.000017135582,0.00025190497,0.00005055802,0.0040442836,0.9564739,0.00038138332,0.0030922336,0.0000053643766],"about_ca_topic_score_codex":0.0017973694,"about_ca_topic_score_gemma":0.0026921737,"teacher_disagreement_score":0.0017973694,"about_ca_system_score_codex":0.0003430924,"about_ca_system_score_gemma":0.0001929282,"threshold_uncertainty_score":0.003573835},"labels":[],"label_agreement":null},{"id":"W2007846880","doi":"10.1038/ng.254","title":"Lung cancer susceptibility locus at 5p15.33","year":2008,"lang":"en","type":"article","venue":"Nature Genetics","topic":"RNA modifications and cancer","field":"Biochemistry, Genetics and Molecular Biology","cited_by":569,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Princess Margaret Cancer Centre; McGill University and Génome Québec Innovation Centre; Ontario Institute for Cancer Research; Women's College Hospital; Cancer Care Ontario; Lunenfeld-Tanenbaum Research Institute","funders":"National Cancer Institute","keywords":"Lung cancer; Biology; Genome-wide association study; Lung cancer susceptibility; Locus (genetics); Genome; Genetics; Gene; Bioinformatics; Oncology; Single-nucleotide polymorphism; Medicine; Genotype","score_opus":0.009205207705480157,"score_gpt":0.2832908759667088,"score_spread":0.27408566826122865,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2007846880","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.97286737,0.0033655008,0.006864558,0.0010856725,0.0002612571,0.00009564023,0.0023519734,0.00054728193,0.012560732],"genre_scores_gemma":[0.994323,0.00025407298,0.0014582901,0.00019249367,0.000024125044,0.000018417732,0.0008921331,0.000016677066,0.00282074],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9998802,0.000024585297,0.0000069444814,0.000031208252,0.0000314517,0.000025616278],"domain_scores_gemma":[0.9998512,0.000039419392,0.000041274667,0.000008725626,0.000011259679,0.00004810449],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00012625118,0.00035489755,0.00023074377,0.0007783073,0.0002503786,0.0002900964,0.0002284973,0.00067036966,0.0082191955],"category_scores_gemma":[0.00024335625,0.00017520347,0.00039724927,0.00028356066,0.00020577341,0.000079536825,0.0002449282,0.00042493828,0.0011314799],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0013158591,0.00009994612,0.031809784,0.00020967964,0.00019862485,0.012866436,0.00019355706,0.0010446715,0.9018486,0.005062186,0.004443717,0.040906854],"study_design_scores_gemma":[0.00034264408,0.00077903183,0.5907825,0.00033255367,0.00039916605,0.027273035,0.00023060202,0.0050204126,0.31128967,0.008590548,0.05487245,0.000087282344],"about_ca_topic_score_codex":0.001966563,"about_ca_topic_score_gemma":0.0019044289,"teacher_disagreement_score":0.0082191955,"about_ca_system_score_codex":0.00027521298,"about_ca_system_score_gemma":0.00023030615,"threshold_uncertainty_score":0.02749592},"labels":[],"label_agreement":null},{"id":"W2008022422","doi":"10.1038/ng.652","title":"Genome-wide association study of migraine implicates a common susceptibility variant on 8q22.1","year":2010,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Migraine and Headache Studies","field":"Medicine","cited_by":407,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Toronto; Centre for Addiction and Mental Health","funders":"Nederlandse Organisatie voor Wetenschappelijk Onderzoek; Wellcome Trust","keywords":"Biology; Genome-wide association study; Genetics; Genetic association; Association (psychology); Migraine; Genome; Computational biology; Genotype; Single-nucleotide polymorphism; Gene; Internal medicine; Medicine","score_opus":0.012352004730305234,"score_gpt":0.3028311760237141,"score_spread":0.2904791712934089,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2008022422","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9964796,0.0014090912,0.00035395505,0.0003878038,0.000051579165,0.000009559976,0.00040699085,0.000015387825,0.0008860175],"genre_scores_gemma":[0.99855894,0.000366569,0.00033801686,0.00008513419,0.00007203057,0.000008004197,0.00026012628,0.0000054193315,0.00030578632],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9990495,0.00034237237,0.000099005396,0.00024955889,0.00015947172,0.0001000844],"domain_scores_gemma":[0.99793124,0.000935754,0.00062190485,0.00014510176,0.00013451921,0.00023145131],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0008318829,0.00072657893,0.0006419806,0.0016335758,0.0007580623,0.0006067505,0.0006623918,0.001229253,0.004623216],"category_scores_gemma":[0.0031535518,0.00024838562,0.0006992272,0.0018617335,0.0005804794,0.0002223129,0.0005472482,0.0008293414,0.00032959922],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0043896167,0.00033405877,0.8970927,0.00018642673,0.002331867,0.007953255,0.0006185338,0.0002759821,0.06382584,0.00067469693,0.0019829907,0.02033397],"study_design_scores_gemma":[0.00021600747,0.00054074585,0.98909026,0.000047663976,0.0010999158,0.004714841,0.00020629866,0.00026545287,0.0018908519,0.00038912837,0.0015215202,0.000017324644],"about_ca_topic_score_codex":0.004622356,"about_ca_topic_score_gemma":0.0062104114,"teacher_disagreement_score":0.004623216,"about_ca_system_score_codex":0.00022684646,"about_ca_system_score_gemma":0.00025030557,"threshold_uncertainty_score":0.015466154},"labels":[],"label_agreement":null},{"id":"W2008047506","doi":"10.1038/ng.2713","title":"Massively parallel decoding of mammalian regulatory sequences supports a flexible organizational model","year":2013,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Genomics and Chromatin Dynamics","field":"Biochemistry, Genetics and Molecular Biology","cited_by":263,"is_retracted":false,"has_abstract":false,"route_ca_aff":false,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"","funders":"Eunice Kennedy Shriver National Institute of Child Health and Human Development; National Institute of Diabetes and Digestive and Kidney Diseases; National Institute of Neurological Disorders and Stroke; National Institute of General Medical Sciences; National Human Genome Research Institute; Canadian Institutes of Health Research; National Institutes of Health","keywords":"Enhancer; Biology; Transcription factor; DNA binding site; Binding site; Regulatory sequence; Computational biology; Reporter gene; Gene; Genetics; Gene expression; Promoter","score_opus":0.005640578546285549,"score_gpt":0.22413018617544048,"score_spread":0.21848960762915492,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2008047506","genre_codex":"methods","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":null,"domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.41715404,0.00036098543,0.5627721,0.0018884924,0.00020701477,0.00004670316,0.00040487753,0.0046043536,0.0125613995],"genre_scores_gemma":[0.9129884,0.00015904965,0.084153704,0.0001713238,0.000059239883,0.000041281906,0.00047644982,0.00036772608,0.0015829299],"study_design_codex":"theoretical_or_conceptual","study_design_gemma":"simulation_or_modeling","domain_scores_codex":[0.9996866,0.000080685524,0.000014740932,0.00009826177,0.00007867984,0.000041018673],"domain_scores_gemma":[0.9988949,0.00045379993,0.00007748701,0.00039068458,0.0000990815,0.00008407189],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00049448374,0.0003553739,0.00043722417,0.00027838824,0.00061741954,0.0013242057,0.00093222916,0.0009376705,0.0021304514],"category_scores_gemma":[0.0026575604,0.00043440287,0.00045834854,0.00044527507,0.000855002,0.0014689344,0.00074336666,0.0011861088,0.0009844018],"study_design_candidate":"simulation_or_modeling","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00066932675,0.00022063382,0.004518356,0.00015646624,0.00006828975,0.0004662958,0.0004676296,0.23224424,0.3229093,0.32943505,0.0049104025,0.10393397],"study_design_scores_gemma":[0.000032071435,0.00009624868,0.0012647373,0.000012170784,0.000018501645,0.00009719125,0.000077137556,0.78821474,0.045770887,0.15977769,0.004602254,0.000036379424],"about_ca_topic_score_codex":0.001186831,"about_ca_topic_score_gemma":0.0020095157,"teacher_disagreement_score":0.0021304514,"about_ca_system_score_codex":0.0005826428,"about_ca_system_score_gemma":0.00067061436,"threshold_uncertainty_score":0.0071270466},"labels":[],"label_agreement":null},{"id":"W2009144436","doi":"10.1038/ng1333","title":"Assessing the impact of population stratification on genetic association studies","year":2004,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Genetic Associations and Epidemiology","field":"Biochemistry, Genetics and Molecular Biology","cited_by":822,"is_retracted":false,"has_abstract":false,"route_ca_aff":false,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"","funders":"Canadian Institutes of Health Research; National Institutes of Health; National Alliance for Research on Schizophrenia and Depression; Systematics Association; Bristol-Myers Squibb; Takeda Oncology; U.S. Department of Defense","keywords":"Population stratification; Biology; Stratification (seeds); Genetic association; Population; Cohort; Genotyping; Ancestry-informative marker; Evolutionary biology; Genetics; Allele; Demography; Allele frequency; Genotype; Gene; Single-nucleotide polymorphism; Internal medicine; Medicine","score_opus":0.023043305827521045,"score_gpt":0.37859473068284316,"score_spread":0.3555514248553221,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2009144436","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":"methods","model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":"methods","domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.82093096,0.013217645,0.14321645,0.009158398,0.0010757153,0.0004657838,0.0014108996,0.00039945397,0.010124756],"genre_scores_gemma":[0.9773018,0.0007751738,0.019644627,0.0011851379,0.00032372103,0.00009619004,0.00028175276,0.00006636811,0.00032517806],"study_design_codex":"observational","study_design_gemma":"simulation_or_modeling","domain_scores_codex":[0.5892275,0.37602758,0.011482438,0.009003632,0.01222927,0.002029588],"domain_scores_gemma":[0.2201761,0.71355516,0.020818932,0.036474302,0.006821574,0.0021538753],"candidate_categories":["metaresearch"],"consensus_categories":["metaresearch"],"category_scores_codex":[0.21315293,0.0014586743,0.0020022783,0.0027609514,0.0024781073,0.0030663905,0.0017854298,0.0029289285,0.0014887148],"category_scores_gemma":[0.5116254,0.0010189639,0.003605074,0.0051972,0.0047807754,0.003489564,0.003737506,0.0035499176,0.0002540631],"study_design_candidate":"simulation_or_modeling","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00277922,0.00018142011,0.9016942,0.00043599226,0.010492824,0.0012146985,0.001144307,0.009766472,0.0025578118,0.007021583,0.0014982369,0.06121319],"study_design_scores_gemma":[0.0007543304,0.003725225,0.8296584,0.00047758385,0.01850957,0.002923564,0.0009258265,0.06971953,0.0053927763,0.057320863,0.010305058,0.0002872552],"about_ca_topic_score_codex":0.005074569,"about_ca_topic_score_gemma":0.009319354,"teacher_disagreement_score":0.78684705,"about_ca_system_score_codex":0.0011896624,"about_ca_system_score_gemma":0.0025099362,"threshold_uncertainty_score":0.97032255},"labels":[],"label_agreement":null},{"id":"W2009163705","doi":"10.1038/ng1348","title":"Just-in-time transcription program in metabolic pathways","year":2004,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Gene Regulatory Network Analysis","field":"Biochemistry, Genetics and Molecular Biology","cited_by":489,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Calgary","funders":"National Institutes of Health","keywords":"Biology; Synthetic biology; Transcription (linguistics); Gene; Computational biology; Transcription factor; Promoter; Gene expression; Regulation of gene expression; Reporter gene; Metabolic pathway; Systems biology; Genetics; Metabolic engineering","score_opus":0.0073190992040908205,"score_gpt":0.24205933999534782,"score_spread":0.234740240791257,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2009163705","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.59263927,0.0004341503,0.3965345,0.0008548902,0.00013369309,0.000047110192,0.0011179113,0.0010607367,0.0071777934],"genre_scores_gemma":[0.97360176,0.0001602536,0.023048012,0.000063819425,0.000044846252,0.000037637557,0.00044926666,0.00011812124,0.0024763148],"study_design_codex":"theoretical_or_conceptual","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9996642,0.00008466337,0.00001351825,0.00011723826,0.0000630696,0.00005745385],"domain_scores_gemma":[0.99864894,0.0006904444,0.0001371225,0.00022518486,0.00015112387,0.00014725189],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00041809186,0.0002299908,0.00034878362,0.0003701808,0.00032857456,0.0008910071,0.00059789524,0.00033332518,0.0024267742],"category_scores_gemma":[0.002177159,0.00021135187,0.00034997033,0.0004509374,0.0005050867,0.0015670042,0.00039660165,0.0006368191,0.0003289864],"study_design_candidate":"bench_or_experimental","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0023323714,0.00026660127,0.016794391,0.0002847588,0.000075874974,0.0005621666,0.0004423869,0.0651233,0.37511116,0.45254433,0.0027760495,0.08368653],"study_design_scores_gemma":[0.00013440441,0.0002447692,0.013139079,0.000026953732,0.00008925139,0.000679966,0.00022023021,0.38197026,0.1395451,0.45681643,0.0070536938,0.00007990866],"about_ca_topic_score_codex":0.00053716503,"about_ca_topic_score_gemma":0.0013801877,"teacher_disagreement_score":0.0024267742,"about_ca_system_score_codex":0.0004426339,"about_ca_system_score_gemma":0.00049022405,"threshold_uncertainty_score":0.008118391},"labels":[],"label_agreement":null},{"id":"W2010203932","doi":"10.1038/ng.275","title":"Ulcerative colitis–risk loci on chromosomes 1p36 and 12q15 found by genome-wide association study","year":2009,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Inflammatory Bowel Disease","field":"Biochemistry, Genetics and Molecular Biology","cited_by":393,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Hôpital du Saint-Sacrement; Hôpital Saint-Luc; Hospital for Sick Children; Princess Margaret Cancer Centre; Montreal Heart Institute; Université Laval; Université de Montréal; University of Toronto; Mount Sinai Hospital","funders":"National Center for Research Resources; National Institute of Diabetes and Digestive and Kidney Diseases; National Center for Advancing Translational Sciences; National Institute of Mental Health","keywords":"Biology; Ulcerative colitis; Genome-wide association study; Locus (genetics); Odds ratio; Genetics; Chromosome; Inflammatory bowel disease; Population; Genome; Disease; Genotype; Internal medicine; Single-nucleotide polymorphism; Gene; Medicine","score_opus":0.0034033127179380995,"score_gpt":0.2377746574461379,"score_spread":0.23437134472819982,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2010203932","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99363846,0.003674068,0.00074243697,0.00046978044,0.000054680368,0.000021355732,0.00046986307,0.000039849616,0.0008894629],"genre_scores_gemma":[0.99759275,0.00051562657,0.00084795285,0.00008283641,0.0000454931,0.00001088113,0.00030641834,0.0000069916796,0.000590977],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99931324,0.00019252622,0.00007254207,0.00021131865,0.00012787041,0.00008251495],"domain_scores_gemma":[0.9988819,0.0003528354,0.0003890879,0.000099812176,0.00011696891,0.00015942368],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.000799632,0.00061313726,0.00085877004,0.0023605644,0.00065449387,0.0007089515,0.00078285893,0.0009595777,0.0035624397],"category_scores_gemma":[0.0026406995,0.00038725475,0.0010240722,0.0025707432,0.00046019163,0.00022938485,0.0006270049,0.00073675386,0.00041258783],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.009111647,0.00029177457,0.882185,0.00027281145,0.0023951414,0.0059079286,0.0005505401,0.0006123313,0.063978806,0.00050995895,0.0017173191,0.03246669],"study_design_scores_gemma":[0.00025481687,0.00028532255,0.9877747,0.000044068795,0.0013849237,0.004493928,0.00015019104,0.0004963859,0.002424843,0.000525992,0.002141333,0.00002347428],"about_ca_topic_score_codex":0.006176732,"about_ca_topic_score_gemma":0.0062104496,"teacher_disagreement_score":0.006176732,"about_ca_system_score_codex":0.00030378412,"about_ca_system_score_gemma":0.00028255835,"threshold_uncertainty_score":0.012281597},"labels":[],"label_agreement":null},{"id":"W2010378709","doi":"10.1038/ng879","title":"Low-penetrance susceptibility to breast cancer due to CHEK2*1100delC in noncarriers of BRCA1 or BRCA2 mutations","year":2002,"lang":"en","type":"article","venue":"Nature Genetics","topic":"BRCA gene mutations in cancer","field":"Biochemistry, Genetics and Molecular Biology","cited_by":1109,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Institute of Cancer Research; Women's College Hospital; University of Toronto","funders":"Abramson Family Cancer Research Institute; Cancer Research UK; National Cancer Institute; KWF Kankerbestrijding; Deutsche Krebshilfe; Cancer Research Institute","keywords":"CHEK2; Breast cancer; Biology; Penetrance; Checkpoint Kinase 2; Cancer research; Cancer; Ovarian cancer; Mutation; Genetics; Oncology; Internal medicine; Germline mutation; Gene; Cell cycle; Cell cycle checkpoint; Phenotype; Medicine","score_opus":0.00990067067864628,"score_gpt":0.28833130084857045,"score_spread":0.27843063016992414,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2010378709","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9989755,0.00008701061,0.00024949425,0.000060922805,0.0000092288,0.0000121321045,0.00010140839,0.000019151043,0.00048515602],"genre_scores_gemma":[0.9992173,0.000037865284,0.00012366982,0.000020127984,0.000016284943,0.0000060109714,0.00009939632,0.000013526041,0.00046577342],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99954516,0.00013647444,0.0000536116,0.000094964824,0.00006621512,0.00010346637],"domain_scores_gemma":[0.9983719,0.00070192025,0.00035870753,0.00012047853,0.00008309504,0.00036397646],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0005323668,0.0013169196,0.0008044147,0.002565745,0.0010022427,0.00052366464,0.0007017453,0.0010836321,0.006081844],"category_scores_gemma":[0.0030448982,0.0005250651,0.0005882296,0.0009267133,0.00080961967,0.00044764197,0.0005957837,0.0008225176,0.0006547896],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0073817447,0.0011186627,0.7129799,0.0001412574,0.0003035221,0.10751441,0.0027218927,0.00046360536,0.15483603,0.0008553967,0.0008670569,0.010816492],"study_design_scores_gemma":[0.00021925509,0.0021705325,0.85718703,0.00002907517,0.0002890357,0.1287327,0.0008354461,0.0017424835,0.007008186,0.00075781863,0.00094037456,0.00008799246],"about_ca_topic_score_codex":0.0041774847,"about_ca_topic_score_gemma":0.0025297909,"teacher_disagreement_score":0.006081844,"about_ca_system_score_codex":0.00027521615,"about_ca_system_score_gemma":0.000229936,"threshold_uncertainty_score":0.020345807},"labels":[],"label_agreement":null},{"id":"W2010394110","doi":"10.1038/ng.2849","title":"Fusion of TTYH1 with the C19MC microRNA cluster drives expression of a brain-specific DNMT3B isoform in the embryonal brain tumor ETMR","year":2013,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Epigenetics and DNA Methylation","field":"Biochemistry, Genetics and Molecular Biology","cited_by":202,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Montreal Children's Hospital; McGill University Health Centre; SickKids Foundation; University of Calgary; McGill University; McGill University and Génome Québec Innovation Centre; Hospital for Sick Children; McGill Genome Centre","funders":"Canadian Institutes of Health Research","keywords":"DNMT3B; Biology; Epigenetics; Gene isoform; Downregulation and upregulation; microRNA; DNA methylation; Methylation; Cancer research; Molecular biology; Cell biology; Gene expression; Genetics; Gene","score_opus":0.005221145101859324,"score_gpt":0.23265708340709887,"score_spread":0.22743593830523953,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2010394110","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9907755,0.00043485037,0.0055740206,0.00014986291,0.00004265325,0.000032094737,0.00046782236,0.00014642975,0.0023767622],"genre_scores_gemma":[0.99069715,0.00021679894,0.003093372,0.000035429246,0.00000776932,0.00002162071,0.0005117424,0.00011903475,0.005296991],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99976355,0.000024239771,0.000027702548,0.00006349115,0.00006733931,0.000053678876],"domain_scores_gemma":[0.9996997,0.00009768535,0.00008157162,0.000039670827,0.00001711828,0.00006431104],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00022800939,0.000267002,0.00020612136,0.00030874164,0.00033355213,0.00041224106,0.0003513195,0.0004465758,0.0019983002],"category_scores_gemma":[0.00024239386,0.00038547613,0.00030025546,0.00016782933,0.00032131307,0.00019831728,0.00038847642,0.00089762494,0.00083353533],"study_design_candidate":"bench_or_experimental","study_design_consensus":"bench_or_experimental","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.000026421418,0.000005254443,0.00009485417,0.000006048392,0.0000021674,0.000060232982,0.000015443578,0.000052366966,0.99911207,0.00029051688,0.000029326224,0.00030532558],"study_design_scores_gemma":[0.000010745213,0.000041284286,0.002310414,0.0000020001728,0.000007777058,0.00026209865,0.00002418125,0.001249883,0.9941572,0.000054771765,0.0018751739,0.0000043514815],"about_ca_topic_score_codex":0.0030997999,"about_ca_topic_score_gemma":0.0049288445,"teacher_disagreement_score":0.0030997999,"about_ca_system_score_codex":0.00078924076,"about_ca_system_score_gemma":0.00036478214,"threshold_uncertainty_score":0.0066850185},"labels":[],"label_agreement":null},{"id":"W2011116207","doi":"10.1038/ng.258","title":"The mitochondrial DNA genetic bottleneck results from replication of a subpopulation of genomes","year":2008,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Mitochondrial Function and Pathology","field":"Biochemistry, Genetics and Molecular Biology","cited_by":468,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"McGill University; Montreal Neurological Institute and Hospital","funders":"Eunice Kennedy Shriver National Institute of Child Health and Human Development; Howard Hughes Medical Institute","keywords":"Biology; Heteroplasmy; Genetics; Mitochondrial DNA; Germline; Oogenesis; Oocyte; Embryo; Gene","score_opus":0.012788044510189491,"score_gpt":0.25226174795239514,"score_spread":0.23947370344220564,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2011116207","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.96838135,0.0015969661,0.026731309,0.0008525047,0.00015246285,0.00003248221,0.000529572,0.00046085304,0.0012624189],"genre_scores_gemma":[0.99212646,0.0006565167,0.005250358,0.00018111065,0.0000726283,0.00002614821,0.00054677535,0.00011145248,0.001028434],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99959046,0.00005582574,0.000044866527,0.00016114677,0.00009212671,0.000055582434],"domain_scores_gemma":[0.99843127,0.00049530226,0.00035021847,0.00024722627,0.0001695692,0.00030641802],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.001006203,0.00048813832,0.0009422873,0.00059249054,0.00049319345,0.00093348103,0.00088309095,0.0010794593,0.0013447739],"category_scores_gemma":[0.0021739346,0.00053584285,0.00050625217,0.0004153595,0.0008042575,0.0019247496,0.0010102494,0.001951537,0.00091997435],"study_design_candidate":"bench_or_experimental","study_design_consensus":"bench_or_experimental","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00037421912,0.000048968337,0.00749465,0.0001233039,0.000068110014,0.00065339205,0.00012465047,0.0009811032,0.97957855,0.0036990785,0.0003541647,0.0064998283],"study_design_scores_gemma":[0.00023164104,0.0010029929,0.06211105,0.00008250953,0.00028849204,0.008010586,0.0003778783,0.01998472,0.8755714,0.015647758,0.01652997,0.00016106246],"about_ca_topic_score_codex":0.0004879711,"about_ca_topic_score_gemma":0.00043501746,"teacher_disagreement_score":0.0013447739,"about_ca_system_score_codex":0.00068479916,"about_ca_system_score_gemma":0.00065715716,"threshold_uncertainty_score":0.0053213835},"labels":[],"label_agreement":null},{"id":"W2011920499","doi":"10.1038/ng.259","title":"Deep surveying of alternative splicing complexity in the human transcriptome by high-throughput sequencing","year":2008,"lang":"en","type":"article","venue":"Nature Genetics","topic":"RNA Research and Splicing","field":"Biochemistry, Genetics and Molecular Biology","cited_by":4023,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Toronto","funders":"","keywords":"Biology; Alternative splicing; RNA splicing; Exon; splice; Transcriptome; Computational biology; Gene expression profiling; RNA-Seq; Genetics; Gene; Complementary DNA; Human genome; Gene expression; Genome; RNA","score_opus":0.04719731054958918,"score_gpt":0.3218389374974995,"score_spread":0.2746416269479103,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2011920499","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9352978,0.0019568321,0.0576003,0.0003894393,0.000024453553,0.000019334488,0.0031431133,0.0002803685,0.0012883317],"genre_scores_gemma":[0.96308035,0.0010814408,0.030899469,0.00022537455,0.000052000178,0.00003684324,0.003650408,0.000095801624,0.0008782456],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99978906,0.00004539511,0.00001047066,0.0000698731,0.00005573713,0.00002936908],"domain_scores_gemma":[0.99940133,0.0003229172,0.00007437281,0.00008283849,0.0000708029,0.00004785307],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00044883578,0.00024270397,0.0005103316,0.00046537872,0.00032205647,0.00057857845,0.00020331606,0.00045163298,0.00040613825],"category_scores_gemma":[0.0008180193,0.0003111369,0.00045877756,0.0004945594,0.00029331466,0.00036022929,0.0003994596,0.00068774825,0.00018917893],"study_design_candidate":"bench_or_experimental","study_design_consensus":"bench_or_experimental","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00035717318,0.00003308121,0.026723277,0.00019980816,0.00025796532,0.00022582964,0.00026099468,0.009747675,0.92511743,0.0017180607,0.00092494086,0.034433737],"study_design_scores_gemma":[0.00006271613,0.00031109908,0.50486,0.000070762144,0.0005678482,0.0022297835,0.0004706182,0.17432626,0.27841073,0.020492096,0.01806789,0.00013017013],"about_ca_topic_score_codex":0.0010823739,"about_ca_topic_score_gemma":0.0028607857,"teacher_disagreement_score":0.0010823739,"about_ca_system_score_codex":0.00022600364,"about_ca_system_score_gemma":0.00025210835,"threshold_uncertainty_score":0.0023736954},"labels":[],"label_agreement":null},{"id":"W2012987716","doi":"10.1038/ng1994","title":"The Shwachman-Bodian-Diamond syndrome protein mediates translational activation of ribosomes in yeast","year":2007,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Blood disorders and treatments","field":"Biochemistry, Genetics and Molecular Biology","cited_by":339,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Toronto","funders":"","keywords":"Ribosome; Biology; Ribosomal protein; Eukaryotic Large Ribosomal Subunit; Ribosomal RNA; Eukaryotic Small Ribosomal Subunit; Translation (biology); Genetics; Protein subunit; Yeast; Cell biology; Gene; RNA; Messenger RNA","score_opus":0.004436137592532903,"score_gpt":0.2405029474676939,"score_spread":0.23606680987516102,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2012987716","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9886972,0.00233149,0.0068562184,0.000370801,0.00011813308,0.000022665592,0.00023995306,0.00029020564,0.001073356],"genre_scores_gemma":[0.9952213,0.00064161635,0.0025762317,0.000059044014,0.000013121161,0.000013505536,0.00035863445,0.00008766269,0.001028678],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9998055,0.000045171895,0.000025911851,0.000043452244,0.00004664569,0.000033433786],"domain_scores_gemma":[0.999676,0.0001161621,0.00006548529,0.00004993159,0.000021760414,0.00007052283],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00035194805,0.0007043701,0.00050499954,0.00035515055,0.00041908343,0.00065748196,0.00041709584,0.0006088902,0.000818424],"category_scores_gemma":[0.0003515636,0.0003169414,0.00041169245,0.00026314374,0.00056799065,0.00034666233,0.00057384,0.001099904,0.0008087838],"study_design_candidate":"bench_or_experimental","study_design_consensus":"bench_or_experimental","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00030699043,0.000024913927,0.00040670403,0.000067608395,0.000012700492,0.00040147846,0.0000396852,0.00036674924,0.9946896,0.0013056155,0.0002590783,0.0021189968],"study_design_scores_gemma":[0.000052399784,0.000083063656,0.001982385,0.000007693962,0.000019725341,0.0005405561,0.0000641159,0.003366129,0.99011517,0.0005871081,0.0031655019,0.000016176276],"about_ca_topic_score_codex":0.0013598748,"about_ca_topic_score_gemma":0.0014577695,"teacher_disagreement_score":0.0013598748,"about_ca_system_score_codex":0.0007576279,"about_ca_system_score_gemma":0.00038464725,"threshold_uncertainty_score":0.0054970384},"labels":[],"label_agreement":null},{"id":"W2013504017","doi":"10.1038/ng.2962","title":"Rare and low-frequency coding variants in CXCR2 and other genes are associated with hematological traits","year":2014,"lang":"en","type":"review","venue":"Nature Genetics","topic":"Blood disorders and treatments","field":"Biochemistry, Genetics and Molecular Biology","cited_by":139,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Montreal Heart Institute","funders":"National Institute of Allergy and Infectious Diseases; National Human Genome Research Institute; National Cancer Institute; National Heart, Lung, and Blood Institute; National Institutes of Health","keywords":"Biology; Hematocrit; Missense mutation; Genetics; Frameshift mutation; Exome; Genome-wide association study; Exome sequencing; White blood cell; Immunology; Mutation; Gene; Single-nucleotide polymorphism; Genotype; Endocrinology","score_opus":0.014460418156651599,"score_gpt":0.27442924860014556,"score_spread":0.25996883044349395,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2013504017","genre_codex":"review","genre_gemma":"review","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"review","genre_consensus":"review","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.00041536888,0.99743986,0.00040206057,0.0005819604,0.00022083377,0.0000042824804,0.000055509947,0.000010909853,0.000869158],"genre_scores_gemma":[0.0030103144,0.99387497,0.0007898002,0.0006915204,0.00050861837,0.00000981563,0.00013656881,0.000003419833,0.00097484625],"study_design_codex":"design_other","study_design_gemma":"systematic_review","domain_scores_codex":[0.9998392,0.000028279208,0.000023591869,0.00003850376,0.000055030938,0.000015310436],"domain_scores_gemma":[0.99970466,0.00018119357,0.00004138334,0.000007677961,0.00004531913,0.000019781966],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00048803084,0.00068253576,0.0010120122,0.0008697088,0.00011823874,0.00055123307,0.0006347008,0.0007698386,0.0020871002],"category_scores_gemma":[0.0007756337,0.00016092989,0.00038695434,0.0008645472,0.0003500943,0.00039556235,0.00036965517,0.0011722232,0.00060214486],"study_design_candidate":"systematic_review","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00013975057,0.000032506447,0.001679109,0.005539617,0.00020300978,0.00058156735,0.000026678325,0.00030993964,0.0018840462,0.0023057878,0.028644687,0.95865333],"study_design_scores_gemma":[0.00010028099,0.0000980967,0.007795827,0.004046084,0.0006712419,0.0073122066,0.00007935829,0.00024361275,0.0012344216,0.003928442,0.974446,0.000044528962],"about_ca_topic_score_codex":0.0008941738,"about_ca_topic_score_gemma":0.0018089776,"teacher_disagreement_score":0.0020871002,"about_ca_system_score_codex":0.00032756806,"about_ca_system_score_gemma":0.00062395004,"threshold_uncertainty_score":0.0069820285},"labels":[],"label_agreement":null},{"id":"W2013981603","doi":"10.1038/ng1413","title":"Abnormal TNF activity in Timp3−/− mice leads to chronic hepatic inflammation and failure of liver regeneration","year":2004,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Hepatitis B Virus Studies","field":"Medicine","cited_by":283,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Toronto; Ontario Institute for Cancer Research","funders":"","keywords":"Tumor necrosis factor alpha; Biology; Inflammation; Hepatocyte; Cytokine; Liver regeneration; Liver injury; Immunology; Necrosis; Endocrinology; Internal medicine; Regeneration (biology); Medicine; Cell biology","score_opus":0.008781912366857724,"score_gpt":0.2582568583837505,"score_spread":0.2494749460168928,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2013981603","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99079365,0.0009344487,0.0043056416,0.0004951497,0.000112090594,0.00003311218,0.0013754015,0.0004062144,0.0015443134],"genre_scores_gemma":[0.98874354,0.0007677445,0.0031262182,0.00015286292,0.00005611041,0.000066302884,0.0007648108,0.0003004315,0.006021919],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9994035,0.00010368767,0.00011442141,0.000118550066,0.00014610721,0.00011379481],"domain_scores_gemma":[0.9985759,0.00015809402,0.0006073596,0.0001447793,0.00005799089,0.00045588665],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0004108977,0.0009956093,0.0005165642,0.0017516987,0.0004501776,0.0008805593,0.00054566347,0.0010582448,0.0054443926],"category_scores_gemma":[0.0004144605,0.000647211,0.00064349733,0.0006008447,0.0010134388,0.0005873213,0.00035597183,0.0026552938,0.0016695703],"study_design_candidate":"bench_or_experimental","study_design_consensus":"bench_or_experimental","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00046016753,0.00004151416,0.00023059604,0.000024296418,0.000009573165,0.00018747522,0.000019417901,0.00003468697,0.9983835,0.00016016471,0.000042365828,0.00040623744],"study_design_scores_gemma":[0.00011992543,0.00041136774,0.0049213893,0.000015288755,0.000057031844,0.0024520261,0.00013007196,0.0006132548,0.98986024,0.000279064,0.0011234723,0.00001698319],"about_ca_topic_score_codex":0.00058325456,"about_ca_topic_score_gemma":0.0006995965,"teacher_disagreement_score":0.0054443926,"about_ca_system_score_codex":0.0004768394,"about_ca_system_score_gemma":0.0002952655,"threshold_uncertainty_score":0.018213272},"labels":[],"label_agreement":null},{"id":"W2014656523","doi":"10.1038/ng.2796","title":"A genome-wide association study identifies new susceptibility loci for esophageal adenocarcinoma and Barrett's esophagus","year":2013,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Esophageal Cancer Research and Treatment","field":"Medicine","cited_by":195,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Saskatchewan; Ontario Institute for Cancer Research","funders":"National Institute of Diabetes and Digestive and Kidney Diseases; National Institute of Allergy and Infectious Diseases; National Human Genome Research Institute; Cancer Research UK; National Cancer Institute; National Institute for Health and Care Research; Wellcome Trust","keywords":"Esophagus; Adenocarcinoma; Biology; Barrett's esophagus; Esophageal cancer; Dysplasia; Cancer research; Internal medicine; Gastroenterology; Cancer; Medicine; Genetics; Anatomy","score_opus":0.014884210196263955,"score_gpt":0.30294539199320075,"score_spread":0.2880611817969368,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2014656523","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9971732,0.0010384253,0.0006186146,0.0002407737,0.00003586055,0.000008734764,0.00032708736,0.000024275298,0.0005329423],"genre_scores_gemma":[0.9983386,0.0003107901,0.0005923477,0.00007249469,0.00003555722,0.0000067350734,0.00031160447,0.000013096274,0.00031869442],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99934834,0.0001859547,0.00007008557,0.00021225802,0.00010626265,0.00007709215],"domain_scores_gemma":[0.9985008,0.000618487,0.0003224103,0.00016515753,0.000115406125,0.00027764312],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00087708666,0.00063792313,0.00053148915,0.0016515463,0.0008402967,0.0008003894,0.00064310676,0.0010337717,0.0023856007],"category_scores_gemma":[0.002173003,0.0004616019,0.001209876,0.0019067789,0.00060151506,0.0003382381,0.00071619556,0.0011027219,0.00020682655],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.003825458,0.00031474725,0.93044764,0.000089986606,0.0021857594,0.0023151978,0.00030749058,0.0001678102,0.05114452,0.0002236199,0.0005692421,0.00840855],"study_design_scores_gemma":[0.00013063817,0.00022397618,0.99474573,0.000008988752,0.0009143096,0.0018555949,0.0001231919,0.00023203796,0.0010539222,0.0001575746,0.00054165267,0.000012325447],"about_ca_topic_score_codex":0.0033167072,"about_ca_topic_score_gemma":0.005632225,"teacher_disagreement_score":0.0033167072,"about_ca_system_score_codex":0.00020506886,"about_ca_system_score_gemma":0.00034432183,"threshold_uncertainty_score":0.007980585},"labels":[],"label_agreement":null},{"id":"W2015213608","doi":"10.1038/ng1470","title":"Comparison of genome degradation in Paratyphi A and Typhi, human-restricted serovars of Salmonella enterica that cause typhoid","year":2004,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Salmonella and Campylobacter epidemiology","field":"Agricultural and Biological Sciences","cited_by":398,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Calgary","funders":"National Institute of Allergy and Infectious Diseases","keywords":"Biology; Salmonella typhi; Genome; Serotype; Pseudogene; Salmonella enterica; Typhoid fever; Genetics; Gene; Microbiology; Salmonella; Virology; Bacteria; Escherichia coli","score_opus":0.05338904621001368,"score_gpt":0.3164749920487064,"score_spread":0.2630859458386927,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2015213608","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9973018,0.0005213786,0.00052005047,0.000040210558,0.000010305123,0.0000036892295,0.0009329355,0.000013222959,0.00065629976],"genre_scores_gemma":[0.9945285,0.0001889026,0.00044725018,0.000067640845,0.0000059478803,0.000007840787,0.0034008177,0.00001966472,0.0013333583],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.99980456,0.000028146447,0.000012184117,0.000049507973,0.000043810127,0.00006177806],"domain_scores_gemma":[0.99933356,0.00015576629,0.00014859637,0.000059151876,0.00016402364,0.00013886971],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00019007485,0.00019933283,0.00034731996,0.00053462404,0.00026850126,0.0004223422,0.00016122372,0.0004664475,0.0016129006],"category_scores_gemma":[0.00067319244,0.00016155103,0.00044015353,0.0003083766,0.0002124672,0.0002558866,0.00022076712,0.0004935589,0.00040381364],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0014115768,0.00003962158,0.007965228,0.000045240376,0.000028350474,0.0000598643,0.00008515722,0.00010217892,0.9883426,0.00007809742,0.0000874603,0.0017545942],"study_design_scores_gemma":[0.000034692453,0.0013567719,0.6450376,0.000013098284,0.00009685163,0.0011555734,0.00047583427,0.0020703783,0.34655446,0.00017690173,0.003007457,0.000020417372],"about_ca_topic_score_codex":0.0020551786,"about_ca_topic_score_gemma":0.0017573268,"teacher_disagreement_score":0.0020551786,"about_ca_system_score_codex":0.00028666816,"about_ca_system_score_gemma":0.00019199139,"threshold_uncertainty_score":0.0053957105},"labels":[],"label_agreement":null},{"id":"W2015220480","doi":"10.1038/87052","title":"Integrin-linked kinase regulates E-cadherin expression by means of the transcription factor Snail","year":2001,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Mechanisms of cancer metastasis","field":"Biochemistry, Genetics and Molecular Biology","cited_by":0,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of British Columbia; BC Cancer Agency","funders":"","keywords":"Snail; Biology; Transcription factor; Cell biology; Cadherin; Integrin; Genetics; Cell; Gene; Ecology","score_opus":0.01108812901538053,"score_gpt":0.25143773833392435,"score_spread":0.24034960931854382,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2015220480","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9873169,0.0018635155,0.005436468,0.00025199083,0.000030452868,0.0000096694175,0.00013020854,0.00010725626,0.0048533585],"genre_scores_gemma":[0.99686015,0.00045475626,0.00060835533,0.000035479654,0.000006110381,0.000005210098,0.00007583638,0.00001680431,0.0019373478],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9998758,0.000021527612,0.0000069717503,0.00002214553,0.00002853346,0.000045154826],"domain_scores_gemma":[0.99991226,0.000020237989,0.000023184632,0.000012369713,0.000009422477,0.000022487799],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00013333073,0.00016141677,0.00014367588,0.00016072243,0.00019527583,0.00047378094,0.00015871157,0.00017418488,0.0008783859],"category_scores_gemma":[0.00020831407,0.00020417044,0.00020815166,0.00010746919,0.0003002002,0.0003251093,0.00034317124,0.00043627806,0.0003741989],"study_design_candidate":"bench_or_experimental","study_design_consensus":"bench_or_experimental","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00012515127,0.000011403735,0.0006889605,0.000013566366,0.000004067857,0.00007696792,0.000026075297,0.00016892771,0.9961635,0.0010185305,0.00008013096,0.0016227921],"study_design_scores_gemma":[0.00004959073,0.00014346557,0.03285127,0.0000105059335,0.000026999629,0.00061830564,0.00013888632,0.0071457927,0.95208085,0.0010476388,0.0058705434,0.000016180778],"about_ca_topic_score_codex":0.0003709525,"about_ca_topic_score_gemma":0.0007936837,"teacher_disagreement_score":0.0008783859,"about_ca_system_score_codex":0.00032654658,"about_ca_system_score_gemma":0.00011827506,"threshold_uncertainty_score":0.002938509},"labels":[],"label_agreement":null},{"id":"W2015410907","doi":"10.1038/ng.3105","title":"Genome-wide association study identifies multiple susceptibility loci for diffuse large B cell lymphoma","year":2014,"lang":"en","type":"review","venue":"Nature Genetics","topic":"Lymphoma Diagnosis and Treatment","field":"Medicine","cited_by":175,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"BC Cancer Agency","funders":"National Institute of Environmental Health Sciences; National Cancer Institute; National Institutes of Health; World Health Organization; National Human Genome Research Institute; National Center for Advancing Translational Sciences; Purdue University","keywords":"Genome-wide association study; Biology; Diffuse large B-cell lymphoma; Single-nucleotide polymorphism; Genetics; Genetic association; Genotyping; Lymphoma; Genetic predisposition; Genotype; Gene; Immunology","score_opus":0.019576049258113758,"score_gpt":0.31674865271119484,"score_spread":0.2971726034530811,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2015410907","genre_codex":"review","genre_gemma":"review","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"review","genre_consensus":"review","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.00013144831,0.9986615,0.00012475888,0.00052577496,0.00014801473,0.0000025284317,0.000026528876,0.00000650577,0.0003729058],"genre_scores_gemma":[0.0012783279,0.997262,0.00021796433,0.000561226,0.00033892787,0.000004425126,0.000058378504,0.000001458798,0.00027733305],"study_design_codex":"design_other","study_design_gemma":"observational","domain_scores_codex":[0.99972945,0.000046110352,0.00004941605,0.000060422593,0.00009179396,0.000022747201],"domain_scores_gemma":[0.99924135,0.00042400853,0.000114257404,0.000019179977,0.00013994037,0.00006130286],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0008676771,0.0007855544,0.0017492349,0.001775837,0.00019245308,0.00072896783,0.0010771572,0.0010943927,0.0020708188],"category_scores_gemma":[0.0012025882,0.0002922258,0.00059274695,0.0019519086,0.0004799441,0.00077609956,0.0006827007,0.0015286927,0.00083413],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0001376928,0.000046815014,0.0012042695,0.009342052,0.0003119696,0.00033971175,0.000022066486,0.00022452654,0.000961104,0.00131296,0.034439728,0.951657],"study_design_scores_gemma":[0.00014335882,0.00014352257,0.010002353,0.007654529,0.0014804485,0.0038684017,0.000110282934,0.00020313368,0.00066715106,0.0046478854,0.9710113,0.00006762324],"about_ca_topic_score_codex":0.0012450537,"about_ca_topic_score_gemma":0.0027370476,"teacher_disagreement_score":0.0020708188,"about_ca_system_score_codex":0.0005600501,"about_ca_system_score_gemma":0.0010834701,"threshold_uncertainty_score":0.00692755},"labels":[],"label_agreement":null},{"id":"W2016208474","doi":"10.1038/ng0501-42","title":"Susceptibility to mouse cytomegalovirus is associated with deletion of an activating natural killer cell receptor of the C-type lectin superfamily","year":2001,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Immune Cell Function and Interaction","field":"Immunology and Microbiology","cited_by":398,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"McGill University; Ontario Genomics; University of Ottawa","funders":"","keywords":"Biology; Genetics; Major histocompatibility complex; Locus (genetics); Gene; Natural killer cell; Positional cloning; Human cytomegalovirus; Allele; Virology; Molecular biology; Cytotoxic T cell","score_opus":0.009093725737031478,"score_gpt":0.23679970806389572,"score_spread":0.22770598232686423,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2016208474","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99858296,0.00019045413,0.00044738778,0.00003771587,0.000010564606,0.000011287957,0.00016729254,0.000050805425,0.0005014612],"genre_scores_gemma":[0.99876773,0.00014626206,0.00022561708,0.000016768156,0.000009945203,0.000009090496,0.00032749577,0.000023898063,0.00047309705],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9995901,0.000090188376,0.000049002778,0.00007954755,0.00009840317,0.00009276002],"domain_scores_gemma":[0.998679,0.00028733912,0.0005784685,0.00012776219,0.000046648267,0.0002807413],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00019473142,0.00097207836,0.00038504842,0.0012823989,0.00027183513,0.00044700428,0.00042695913,0.0007667705,0.0024425732],"category_scores_gemma":[0.0005384083,0.0003636551,0.000449846,0.00045417476,0.00075481914,0.00020727981,0.00057793385,0.0011651459,0.000563366],"study_design_candidate":"bench_or_experimental","study_design_consensus":"bench_or_experimental","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00055441476,0.000049224593,0.0020301137,0.000020307933,0.000019231291,0.0005930698,0.000029462217,0.000050505125,0.9961145,0.000108072025,0.00003174207,0.0003992422],"study_design_scores_gemma":[0.0003533003,0.0019971095,0.328259,0.00004930259,0.00035845008,0.036084853,0.00035303202,0.002398597,0.62549406,0.0008835541,0.003675466,0.00009324509],"about_ca_topic_score_codex":0.00059816457,"about_ca_topic_score_gemma":0.00046720935,"teacher_disagreement_score":0.0024425732,"about_ca_system_score_codex":0.00028577473,"about_ca_system_score_gemma":0.0001835611,"threshold_uncertainty_score":0.008171201},"labels":[],"label_agreement":null},{"id":"W2016370312","doi":"10.1038/ng.1076","title":"Five amino acids in three HLA proteins explain most of the association between MHC and seropositive rheumatoid arthritis","year":2012,"lang":"en","type":"article","venue":"Nature Genetics","topic":"T-cell and B-cell Immunology","field":"Immunology and Microbiology","cited_by":961,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Toronto; University Health Network; Mount Sinai Hospital","funders":"National Institute of Arthritis and Musculoskeletal and Skin Diseases; National Institute of General Medical Sciences; Wellcome Trust","keywords":"Major histocompatibility complex; Rheumatoid arthritis; Human leukocyte antigen; Biology; Imputation (statistics); Single-nucleotide polymorphism; SNP; Genetics; Allele; Immunology; Haplotype; Genome-wide association study; Gene; Antigen; Genotype","score_opus":0.005844446695867592,"score_gpt":0.21187576995401544,"score_spread":0.20603132325814785,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2016370312","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9919979,0.0017173423,0.004090914,0.00037422217,0.00017577434,0.000025538762,0.00037825442,0.00005941208,0.001180621],"genre_scores_gemma":[0.99661034,0.00029498665,0.002126419,0.00023747506,0.000064370724,0.000009561187,0.0002716803,0.000020783295,0.00036431718],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9996221,0.00010976291,0.000055036362,0.00007690549,0.000077611934,0.000058555066],"domain_scores_gemma":[0.99859864,0.0005593854,0.00041724337,0.00012592349,0.00009902954,0.00019977844],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00055845117,0.0009808639,0.0006583196,0.0009109774,0.00055657246,0.00048098262,0.00063849974,0.0014631498,0.003160488],"category_scores_gemma":[0.00121959,0.0002626582,0.0012241068,0.00079276686,0.0005880979,0.00036246583,0.00039987164,0.0009813799,0.0010466435],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0074141556,0.0006135991,0.23929301,0.0006442003,0.0017277246,0.019461023,0.0006884217,0.0031338488,0.685548,0.0030743706,0.0011945056,0.037207186],"study_design_scores_gemma":[0.00073314353,0.001627561,0.8574797,0.0002743623,0.0026907965,0.028603693,0.000755182,0.009286369,0.08041212,0.0066783885,0.011289789,0.00016895187],"about_ca_topic_score_codex":0.00087519415,"about_ca_topic_score_gemma":0.0007413441,"teacher_disagreement_score":0.003160488,"about_ca_system_score_codex":0.0002615589,"about_ca_system_score_gemma":0.00024782665,"threshold_uncertainty_score":0.010572851},"labels":[],"label_agreement":null},{"id":"W2016631383","doi":"10.1038/ng.1015","title":"Fine points in mapping autoimmunity","year":2011,"lang":"en","type":"letter","venue":"Nature Genetics","topic":"Celiac Disease Research and Management","field":"Medicine","cited_by":18,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"McGill University Health Centre; Montreal Children's Hospital","funders":"","keywords":"Biology; Genotyping; Computational biology; Autoimmunity; Phenotype; Genetics; Evolutionary biology; Genotype; Gene; Immune system","score_opus":0.027090221132340126,"score_gpt":0.29572189739240173,"score_spread":0.2686316762600616,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2016631383","genre_codex":"commentary","genre_gemma":"commentary","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"commentary","genre_consensus":"commentary","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.0018393748,0.005378363,0.0010842773,0.9748071,0.013125056,0.000010663183,0.000035099303,0.000057049765,0.0036629487],"genre_scores_gemma":[0.03503926,0.004354818,0.002223486,0.88582665,0.06735836,0.00005492631,0.000046751502,0.000040145573,0.0050556962],"study_design_codex":"not_applicable","study_design_gemma":"not_applicable","domain_scores_codex":[0.99569523,0.0019569842,0.00036945392,0.00051169086,0.00095590233,0.00051075575],"domain_scores_gemma":[0.9786189,0.015900662,0.0007186334,0.0013248435,0.0015890928,0.0018478304],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0063287085,0.00087365025,0.0017666515,0.0010331868,0.0029847568,0.0029778443,0.0018737126,0.0284563,0.0031023223],"category_scores_gemma":[0.02868655,0.0007521197,0.00089025684,0.00063396414,0.006748815,0.0051743933,0.003116688,0.039496627,0.0018791811],"study_design_candidate":"not_applicable","study_design_consensus":"not_applicable","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00038648382,0.00011294911,0.006329563,0.000271296,0.00016490863,0.01227606,0.0007829772,0.00042585918,0.0026468765,0.030861083,0.852697,0.09304483],"study_design_scores_gemma":[0.00052203296,0.00033368077,0.0062925345,0.0006703848,0.00023400277,0.027665535,0.001565751,0.0016806701,0.0017536875,0.22880803,0.73029155,0.00018218628],"about_ca_topic_score_codex":0.0018867933,"about_ca_topic_score_gemma":0.0032158147,"teacher_disagreement_score":0.0284563,"about_ca_system_score_codex":0.0026444911,"about_ca_system_score_gemma":0.0016433157,"threshold_uncertainty_score":0.033469796},"labels":[],"label_agreement":null},{"id":"W2016631802","doi":"10.1038/ng1238","title":"Mutations in NHLRC1 cause progressive myoclonus epilepsy","year":2003,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Glycogen Storage Diseases and Myoclonus","field":"Medicine","cited_by":326,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"McGill University Health Centre; Montreal General Hospital; McGill University; SickKids Foundation; University of Toronto; Montreal Neurological Institute and Hospital; Hospital for Sick Children","funders":"Canadian Institutes of Health Research; Genome Canada; Fondazione Telethon; Howard Hughes Medical Institute","keywords":"Lafora disease; Progressive myoclonus epilepsy; Epilepsy; Endoplasmic reticulum; Biology; Ubiquitin ligase; Myoclonus; Ring finger; Colocalization; Channelopathy; Mutation; Pathognomonic; Genetics; Ubiquitin; Neuroscience; Gene; Disease; Internal medicine; Medicine","score_opus":0.011225833488124087,"score_gpt":0.2999771050005837,"score_spread":0.2887512715124596,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2016631802","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.98712605,0.0012994998,0.0013370813,0.0010476765,0.00012933963,0.00005054706,0.0006859073,0.00017196074,0.008152061],"genre_scores_gemma":[0.99681854,0.00022494476,0.00048235612,0.00019624259,0.00005162723,0.000013700261,0.00023348031,0.000030907035,0.0019482457],"study_design_codex":"case_report","study_design_gemma":"observational","domain_scores_codex":[0.99983525,0.000022715743,0.000025861615,0.000035604244,0.00004316837,0.000037405527],"domain_scores_gemma":[0.99961627,0.0001534689,0.00009733157,0.00002330906,0.000028329367,0.000081221726],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00015988448,0.000979173,0.00046866076,0.0009453128,0.0005074714,0.0004036427,0.0005290068,0.001995889,0.00414802],"category_scores_gemma":[0.00068736396,0.00025353127,0.00041149138,0.0006275468,0.00068966474,0.0003369165,0.0005892933,0.0006255485,0.0011703756],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0019696276,0.0002729807,0.03956877,0.0002608402,0.00028247802,0.56787986,0.0010182689,0.0011966834,0.3517682,0.0020992926,0.00611244,0.027570507],"study_design_scores_gemma":[0.0008734268,0.00073457096,0.19272417,0.00016199291,0.00066587,0.6366924,0.0011832812,0.00475989,0.13514462,0.0022038883,0.024698032,0.00015791426],"about_ca_topic_score_codex":0.002777094,"about_ca_topic_score_gemma":0.00339865,"teacher_disagreement_score":0.00414802,"about_ca_system_score_codex":0.0007553358,"about_ca_system_score_gemma":0.00029624815,"threshold_uncertainty_score":0.013876438},"labels":[],"label_agreement":null},{"id":"W2016749216","doi":"10.1038/ng.585","title":"Variation in CDKN2A at 9p21.3 influences childhood acute lymphoblastic leukemia risk","year":2010,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Acute Lymphoblastic Leukemia research","field":"Medicine","cited_by":260,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Université de Montréal; Centre Hospitalier Universitaire Sainte-Justine","funders":"National Cancer Institute; National Institute of General Medical Sciences; Cancer Research UK; Wellcome Trust","keywords":"CDKN2A; Biology; Odds ratio; Lymphoblastic Leukemia; Leukemia; Genome-wide association study; Genetics; Internal medicine; Oncology; Single-nucleotide polymorphism; Genotype; Gene; Medicine","score_opus":0.004749406992555375,"score_gpt":0.26564969476906763,"score_spread":0.26090028777651225,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2016749216","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9976954,0.00029470603,0.00026160703,0.00014590466,0.000010681257,0.0000062496088,0.00036578704,0.000011524317,0.0012081793],"genre_scores_gemma":[0.9992392,0.00015393436,0.00014837363,0.00002347457,0.000007718116,0.0000041034255,0.00013534847,0.000011324011,0.0002764663],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99916756,0.00029965144,0.000052381263,0.00023573246,0.00012950746,0.00011516063],"domain_scores_gemma":[0.9988667,0.0005508379,0.00030599232,0.000087573346,0.0000600902,0.00012883218],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0004193362,0.00031272194,0.00024260217,0.00079956953,0.00034171797,0.0006084052,0.000418821,0.0005074977,0.0031481422],"category_scores_gemma":[0.002845421,0.00021766228,0.00042255665,0.001052184,0.0004290213,0.00020573103,0.00033827612,0.00045989014,0.00035496554],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0010264858,0.000047712078,0.9687047,0.000021683016,0.00023006367,0.0010310812,0.00026034177,0.0008459378,0.016468275,0.00057234184,0.000437763,0.01035366],"study_design_scores_gemma":[0.00003096786,0.00007920836,0.99330705,0.000013957858,0.00014563173,0.0013490568,0.00012085067,0.00088631193,0.002626402,0.00050849136,0.0009211919,0.000010749907],"about_ca_topic_score_codex":0.012781646,"about_ca_topic_score_gemma":0.009733926,"teacher_disagreement_score":0.012781646,"about_ca_system_score_codex":0.00054054667,"about_ca_system_score_gemma":0.00033206408,"threshold_uncertainty_score":0.025414526},"labels":[],"label_agreement":null},{"id":"W2016756307","doi":"10.1038/ng904","title":"Protein elongation factor EEF1A2 is a putative oncogene in ovarian cancer","year":2002,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Microtubule and mitosis dynamics","field":"Biochemistry, Genetics and Molecular Biology","cited_by":268,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"McMaster University; University of Calgary","funders":"","keywords":"Biology; Oncogene; Cancer research; Ovarian cancer; Cell culture; Ovarian carcinoma; Elongation; Eukaryotic translation elongation factor 1 alpha 1; Gene; Doubling time; Elongation factor; Molecular biology; Cancer; Cell cycle; Genetics","score_opus":0.009297805893628403,"score_gpt":0.26284647213517925,"score_spread":0.25354866624155087,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2016756307","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.98744166,0.0050322353,0.0036492595,0.00042168176,0.00008878608,0.000020278756,0.0005894517,0.00011555418,0.0026411472],"genre_scores_gemma":[0.9922873,0.0009948645,0.0011898238,0.000059159567,0.000021899044,0.00001185552,0.0012676811,0.000018580973,0.004148887],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9999516,0.000005936605,0.000003776524,0.000014649975,0.000012340658,0.000011553507],"domain_scores_gemma":[0.99992657,0.000012095712,0.000020598645,0.0000075646267,0.000010655297,0.00002253976],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00012165622,0.0002783941,0.00019203588,0.00035021815,0.00034303076,0.0003606067,0.00022228873,0.00034542804,0.0011815964],"category_scores_gemma":[0.00018163289,0.00015714079,0.00020900441,0.00020626666,0.00019193556,0.00021222545,0.00021188072,0.00035051059,0.00039129073],"study_design_candidate":"bench_or_experimental","study_design_consensus":"bench_or_experimental","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.000499625,0.000032579315,0.003729919,0.00008459841,0.000024522134,0.0017499194,0.00002516152,0.00025701267,0.98858345,0.00097131275,0.000444879,0.0035969452],"study_design_scores_gemma":[0.00008161001,0.00024587067,0.05544408,0.0000205449,0.00012307841,0.01049341,0.0001193916,0.0041087945,0.89781654,0.0007490638,0.030779393,0.000018113562],"about_ca_topic_score_codex":0.00092952745,"about_ca_topic_score_gemma":0.0008051777,"teacher_disagreement_score":0.0011815964,"about_ca_system_score_codex":0.00051594514,"about_ca_system_score_gemma":0.00018476747,"threshold_uncertainty_score":0.003952861},"labels":[],"label_agreement":null},{"id":"W2016910640","doi":"10.1038/ng.2331","title":"De novo germline and postzygotic mutations in AKT3, PIK3R2 and PIK3CA cause a spectrum of related megalencephaly syndromes","year":2012,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Genetic and Kidney Cyst Diseases","field":"Biochemistry, Genetics and Molecular Biology","cited_by":753,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Ottawa Hospital; North York General Hospital; Hospital for Sick Children; University of British Columbia; McGill University and Génome Québec Innovation Centre; University of Ottawa; Queen's University; McGill University; University of Calgary; Children's Hospital of Eastern Ontario","funders":"Eunice Kennedy Shriver National Institute of Child Health and Human Development; National Center for Advancing Translational Sciences; McGill University; National Heart, Lung, and Blood Institute; National Institute of Environmental Health Sciences; Canadian Institutes of Health Research; National Institute of Neurological Disorders and Stroke; National Institute of General Medical Sciences; Cancer Research UK","keywords":"Megalencephaly; Biology; Polymicrogyria; Exome sequencing; Genetics; Polydactyly; Context (archaeology); Sanger sequencing; Exome; Mutation; Gene; Neuroscience; Epilepsy","score_opus":0.005595570676620725,"score_gpt":0.2528660547956109,"score_spread":0.2472704841189902,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2016910640","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9973152,0.00024683125,0.00053084345,0.00007705734,0.000010909988,0.000010749565,0.0001285531,0.00003060873,0.0016492108],"genre_scores_gemma":[0.9988274,0.00014679568,0.000374382,0.000030252322,0.000015808868,0.000004645507,0.00010042581,0.000011508732,0.0004886367],"study_design_codex":"case_report","study_design_gemma":"observational","domain_scores_codex":[0.9998493,0.000014972392,0.000020954498,0.00004224452,0.000044614044,0.000027886823],"domain_scores_gemma":[0.99972206,0.00008109811,0.00008693093,0.000019040217,0.000014732601,0.00007615404],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00010976493,0.0011270746,0.00034767826,0.00094484014,0.00039072323,0.00029824267,0.00034016688,0.0006430537,0.002025928],"category_scores_gemma":[0.00053554465,0.00031392757,0.0002967403,0.0007144361,0.0005666105,0.00023401085,0.00061380176,0.00039818935,0.00037037086],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0012884557,0.00025865406,0.12344242,0.0001346415,0.00019483869,0.6138221,0.00060093065,0.00068832503,0.24078004,0.0025648046,0.0010568277,0.015167909],"study_design_scores_gemma":[0.000114719216,0.00027161147,0.23856544,0.000016843851,0.00017558024,0.7385367,0.00021793872,0.00082154287,0.018550389,0.0008861641,0.0018212581,0.000021869837],"about_ca_topic_score_codex":0.0005421529,"about_ca_topic_score_gemma":0.00082116865,"teacher_disagreement_score":0.002025928,"about_ca_system_score_codex":0.00025242826,"about_ca_system_score_gemma":0.00020030583,"threshold_uncertainty_score":0.0067774057},"labels":[],"label_agreement":null},{"id":"W2017308570","doi":"10.1038/ng.336","title":"Multiple recurrent genetic events converge on control of histone lysine methylation in medulloblastoma","year":2009,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Epigenetics and DNA Methylation","field":"Biochemistry, Genetics and Molecular Biology","cited_by":415,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University Health Network; SickKids Foundation; McMaster University; University of Toronto; Hospital for Sick Children","funders":"National Institute of Neurological Disorders and Stroke; National Cancer Institute","keywords":"Biology; EZH2; Histone methylation; Genetics; Histone methyltransferase; Histone; Medulloblastoma; Methylation; Epigenetics; Cancer research; Carcinogenesis; DNA methylation; Gene; Gene expression","score_opus":0.006420681598118842,"score_gpt":0.2906246102605718,"score_spread":0.284203928662453,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2017308570","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9956578,0.0005637192,0.0023540258,0.00007856119,0.000012634474,0.0000069979105,0.00008040459,0.000078252226,0.0011676111],"genre_scores_gemma":[0.99890065,0.00014502693,0.0003970166,0.0000123897535,0.000004956301,0.0000027457988,0.000042510026,0.0000127899975,0.00048193513],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9997851,0.00002233031,0.000019191804,0.000041495237,0.000083006744,0.00004892632],"domain_scores_gemma":[0.9997228,0.000049306836,0.00010175385,0.000045195127,0.00003120304,0.0000497],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00026213558,0.0001945974,0.00036403508,0.0004623256,0.0002792756,0.0004393453,0.0004056063,0.00022856615,0.00073337334],"category_scores_gemma":[0.0005267328,0.00019521013,0.00020073411,0.00030174336,0.00038109586,0.00029452803,0.00047909695,0.0003818956,0.00023170629],"study_design_candidate":"bench_or_experimental","study_design_consensus":"bench_or_experimental","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0003019638,0.0000144625865,0.0058511733,0.000024396273,0.000023945062,0.0006552806,0.00010785513,0.00075883936,0.9853195,0.0018132252,0.00008272632,0.0050466727],"study_design_scores_gemma":[0.000053774475,0.0001961614,0.116948165,0.000010907489,0.0001047478,0.0020415871,0.00023541479,0.0051421844,0.8703483,0.0023760546,0.002506593,0.000036203463],"about_ca_topic_score_codex":0.0027817292,"about_ca_topic_score_gemma":0.004537107,"teacher_disagreement_score":0.0027817292,"about_ca_system_score_codex":0.00072514673,"about_ca_system_score_gemma":0.000292223,"threshold_uncertainty_score":0.005531132},"labels":[],"label_agreement":null},{"id":"W2017760549","doi":"10.1038/ng.373","title":"Mutations involved in Aicardi-Goutières syndrome implicate SAMHD1 as regulator of the innate immune response","year":2009,"lang":"en","type":"article","venue":"Nature Genetics","topic":"interferon and immune responses","field":"Immunology and Microbiology","cited_by":684,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"BC Children's Hospital","funders":"National Institute of Neurological Disorders and Stroke; Manchester Biomedical Research Centre; National Institutes of Health; Newlife the Charity for Disabled Children; NIHR Biomedical Research Centre, Royal Marsden NHS Foundation Trust/Institute of Cancer Research; Wellcome Trust","keywords":"SAMHD1; Biology; Autoimmunity; Regulator; Genetics; Mendelian inheritance; Immune system; Gene; Innate immune system; Locus (genetics); Immunology; RNA; Reverse transcriptase","score_opus":0.006869663857120431,"score_gpt":0.25728623114744764,"score_spread":0.2504165672903272,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2017760549","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9934477,0.0010144593,0.0026446318,0.00044948174,0.0000645186,0.000014166964,0.00015312029,0.000177551,0.0020343622],"genre_scores_gemma":[0.99708647,0.00019649105,0.0020250545,0.00006727444,0.000026727459,0.000006020802,0.000055228313,0.00001543751,0.0005211783],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9998116,0.0000489446,0.000017609389,0.000037884703,0.00005696411,0.000027020573],"domain_scores_gemma":[0.99954885,0.00020392892,0.00012074394,0.000026171696,0.000020830741,0.00007947754],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00017271297,0.0008055246,0.000345957,0.000921553,0.00047363373,0.00039770623,0.00036951408,0.0013380903,0.0021208348],"category_scores_gemma":[0.0007307028,0.00022578266,0.0002639873,0.00039497644,0.0008787024,0.0003056023,0.0003477464,0.000794448,0.0002901116],"study_design_candidate":"bench_or_experimental","study_design_consensus":"bench_or_experimental","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0008890634,0.00006288217,0.037938334,0.00012691661,0.00013658068,0.05617582,0.00041281298,0.0010283198,0.88404596,0.0048980676,0.0010075263,0.013277752],"study_design_scores_gemma":[0.00035164235,0.0004859294,0.30767554,0.00012713557,0.00038826297,0.2858187,0.000581804,0.012706464,0.36700666,0.009338795,0.015398685,0.00012044107],"about_ca_topic_score_codex":0.0009314017,"about_ca_topic_score_gemma":0.001108415,"teacher_disagreement_score":0.0021208348,"about_ca_system_score_codex":0.00038169048,"about_ca_system_score_gemma":0.00019432207,"threshold_uncertainty_score":0.00709486},"labels":[],"label_agreement":null},{"id":"W2018490222","doi":"10.1038/ng2066","title":"Mutations in LCA5, encoding the ciliary protein lebercilin, cause Leber congenital amaurosis","year":2007,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Retinal Development and Disorders","field":"Biochemistry, Genetics and Molecular Biology","cited_by":200,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"McGill University Health Centre","funders":"Wellcome Trust","keywords":"Biology; Cilium; Ciliopathies; Genetics; Ciliogenesis; Bardet–Biedl syndrome; Frameshift mutation; Phenotype; Nonsense mutation; Gene; Cell biology; Missense mutation","score_opus":0.00856596147158855,"score_gpt":0.2603462884518724,"score_spread":0.25178032698028385,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2018490222","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.98539054,0.0034722164,0.0033495012,0.0005586611,0.00019395245,0.00003751884,0.0007077318,0.00027999477,0.0060098483],"genre_scores_gemma":[0.9975827,0.00022723358,0.0010044558,0.000114517024,0.000024369201,0.000004670581,0.00018924146,0.00001883194,0.0008339717],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9997694,0.000020335421,0.000025328218,0.000050379633,0.00009371321,0.00004085723],"domain_scores_gemma":[0.9996189,0.00009873116,0.00013488322,0.000014991542,0.0000255113,0.000106972126],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00010690051,0.0011707653,0.00028946952,0.0012118008,0.0006124291,0.00059405377,0.00029777785,0.0013480387,0.0019550007],"category_scores_gemma":[0.000654125,0.00021994792,0.000327738,0.0005640561,0.0006710754,0.00031489757,0.0005097715,0.00052278885,0.0005202016],"study_design_candidate":"bench_or_experimental","study_design_consensus":"bench_or_experimental","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0008384686,0.000098647135,0.059596628,0.00023448285,0.0002770559,0.09973741,0.00038202383,0.000994097,0.8011319,0.0037610629,0.0029885701,0.029959671],"study_design_scores_gemma":[0.00020881774,0.00037291346,0.31949332,0.00017631706,0.0005980695,0.18812327,0.0007287277,0.009193335,0.45926246,0.0028940823,0.018822046,0.00012665533],"about_ca_topic_score_codex":0.004717769,"about_ca_topic_score_gemma":0.005380662,"teacher_disagreement_score":0.004717769,"about_ca_system_score_codex":0.0010080977,"about_ca_system_score_gemma":0.00034764098,"threshold_uncertainty_score":0.009380639},"labels":[],"label_agreement":null},{"id":"W2019181219","doi":"10.1038/ng844","title":"A mutant PTH/PTHrP type I receptor in enchondromatosis","year":2002,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Bone Tumor Diagnosis and Treatments","field":"Medicine","cited_by":260,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Toronto; Lunenfeld-Tanenbaum Research Institute; Mount Sinai Hospital; Hospital for Sick Children","funders":"","keywords":"Indian hedgehog; Enchondroma; Chondrocyte; Biology; Cartilage; Cancer research; Hedgehog signaling pathway; Dysplasia; Osteochondrodysplasia; Hedgehog; Pathology; Cell biology; Chondrosarcoma; Signal transduction; Anatomy; Genetics; Medicine","score_opus":0.016186391205256064,"score_gpt":0.2665991394633247,"score_spread":0.25041274825806864,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2019181219","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.98887396,0.0037335353,0.0012867914,0.00049703283,0.00013631252,0.000019974912,0.00014686576,0.000115140996,0.005190329],"genre_scores_gemma":[0.99826354,0.00038707387,0.00031859937,0.00007097227,0.000043361484,0.000002750587,0.000036760146,0.000010376669,0.00086667493],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.99984705,0.000015471973,0.000028065195,0.000026822065,0.000038735026,0.000043851996],"domain_scores_gemma":[0.9997931,0.000064221684,0.00005288836,0.000022585356,0.000022287979,0.000044906832],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00017271297,0.00041717876,0.0003297416,0.00076173875,0.0003007078,0.00037213857,0.00045350747,0.0011536375,0.0016934533],"category_scores_gemma":[0.0007156708,0.0001994043,0.00023281976,0.0002619692,0.0005251201,0.0002926267,0.00024519526,0.00040049042,0.00039839096],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0022967898,0.00008017899,0.02113065,0.00015776312,0.00006990789,0.44614252,0.00018865392,0.00052641577,0.51234317,0.0027542522,0.0013604772,0.012949248],"study_design_scores_gemma":[0.00019599586,0.0005801536,0.054141514,0.000028419641,0.000295025,0.8242498,0.0002305193,0.0025471582,0.10854138,0.0014970544,0.0076570786,0.00003597214],"about_ca_topic_score_codex":0.0017888969,"about_ca_topic_score_gemma":0.0011019475,"teacher_disagreement_score":0.0017888969,"about_ca_system_score_codex":0.00036448147,"about_ca_system_score_gemma":0.0002725584,"threshold_uncertainty_score":0.005665183},"labels":[],"label_agreement":null},{"id":"W2019866708","doi":"10.1038/ng1414","title":"Mutations in a member of the Ras superfamily of small GTP-binding proteins causes Bardet-Biedl syndrome","year":2004,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Genetic and Kidney Cyst Diseases","field":"Biochemistry, Genetics and Molecular Biology","cited_by":333,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Memorial University of Newfoundland; Simon Fraser University","funders":"Medical Research Council; Canadian Institutes of Health Research; Michael Smith Health Research BC; National Cancer Institute; National Institutes of Health; March of Dimes Foundation; Children's Hospital Foundation; Wellcome Trust; Heart and Stroke Foundation of Canada","keywords":"Bardet–Biedl syndrome; Biology; Intraflagellar transport; Genetics; GTP-binding protein regulators; Rab; G protein; Cilium; Caenorhabditis elegans; Gene; Small GTPase; Cell biology; GTPase; Signal transduction; Phenotype; Mutant","score_opus":0.00938945774426549,"score_gpt":0.24165911554726832,"score_spread":0.23226965780300282,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2019866708","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99232495,0.0005616822,0.0022678133,0.000851751,0.00013789619,0.00003679906,0.00032237323,0.0002657167,0.003230942],"genre_scores_gemma":[0.9979043,0.00014911896,0.0008149011,0.00011065772,0.00006419762,0.000008002246,0.0000943159,0.000029259892,0.00082527584],"study_design_codex":"case_report","study_design_gemma":"observational","domain_scores_codex":[0.9995479,0.000061867366,0.00004695359,0.00009233961,0.00018862878,0.000062267085],"domain_scores_gemma":[0.9992804,0.00028006002,0.00015282958,0.000026154663,0.000043708977,0.00021683959],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00024401612,0.0018320743,0.0006599803,0.0021096196,0.000828198,0.0004981618,0.00069395226,0.0033035136,0.0023020424],"category_scores_gemma":[0.0012182235,0.00043390732,0.00047766347,0.0010088504,0.0014541051,0.0004631774,0.0007846513,0.0010739998,0.0008362333],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.001246025,0.0002697581,0.029107522,0.00017100906,0.00022869075,0.73592263,0.0011361297,0.00086926937,0.21379621,0.0032536464,0.0021146738,0.011884456],"study_design_scores_gemma":[0.00033084236,0.0005917746,0.10240773,0.000056902456,0.0004398824,0.830367,0.0005309596,0.004699022,0.050674755,0.002166284,0.007580521,0.00015426222],"about_ca_topic_score_codex":0.002010169,"about_ca_topic_score_gemma":0.0020520936,"teacher_disagreement_score":0.0033035136,"about_ca_system_score_codex":0.0005693104,"about_ca_system_score_gemma":0.00042439034,"threshold_uncertainty_score":0.007701099},"labels":[],"label_agreement":null},{"id":"W2019905182","doi":"10.1038/ng.2007.28","title":"RNA toxicity in myotonic muscular dystrophy induces NKX2-5 expression","year":2007,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Genetic Neurodegenerative Diseases","field":"Neuroscience","cited_by":84,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Université Laval","funders":"National Institute of Arthritis and Musculoskeletal and Skin Diseases; University of Miami","keywords":"Myotonic dystrophy; Biology; Transgene; RNA; Muscular dystrophy; Gene expression; Toxicity; Messenger RNA; Gene silencing; Duchenne muscular dystrophy; Myopathy; Connexin; Myotonia; Cell biology; Small interfering RNA; RNA interference; Molecular biology; Gene; Genetics; Internal medicine; Medicine; Gap junction; Intracellular","score_opus":0.01694472193985111,"score_gpt":0.28520419986501605,"score_spread":0.2682594779251649,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2019905182","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.98748374,0.002525524,0.0042043077,0.00040379935,0.00016002658,0.000039784525,0.0007091618,0.00012988795,0.004343743],"genre_scores_gemma":[0.9914478,0.0005309568,0.0015169871,0.00017152814,0.00001860281,0.000035667206,0.00077976997,0.000045375673,0.005453417],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9996244,0.00008161878,0.000052887302,0.00007894778,0.00009377337,0.00006835078],"domain_scores_gemma":[0.9998504,0.000039751496,0.000036405287,0.000017845236,0.0000119484785,0.000043775137],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00024431315,0.00038027568,0.00031216463,0.0004275978,0.00039811342,0.00040556217,0.00022971052,0.00064056297,0.003132512],"category_scores_gemma":[0.00023007218,0.000307492,0.00039064483,0.00014733944,0.00044460682,0.00029094255,0.00044252802,0.0008020068,0.0006758702],"study_design_candidate":"bench_or_experimental","study_design_consensus":"bench_or_experimental","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.000080892256,0.000014695119,0.00017007366,0.00002577235,0.0000072096072,0.00019089736,0.000011551197,0.00009002445,0.9987205,0.00018788328,0.000079431295,0.00042102448],"study_design_scores_gemma":[0.00002564396,0.00020504948,0.008901454,0.000013245209,0.00002745974,0.0011159884,0.00006494171,0.0011290992,0.9862621,0.00015624326,0.0020926169,0.0000061332926],"about_ca_topic_score_codex":0.0011157347,"about_ca_topic_score_gemma":0.0026696345,"teacher_disagreement_score":0.003132512,"about_ca_system_score_codex":0.000633002,"about_ca_system_score_gemma":0.00023895554,"threshold_uncertainty_score":0.010479331},"labels":[],"label_agreement":null},{"id":"W2020372995","doi":"10.1038/ng.224","title":"A canine DNM1 mutation is highly associated with the syndrome of exercise-induced collapse","year":2008,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Cellular transport and secretion","field":"Biochemistry, Genetics and Molecular Biology","cited_by":64,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Saskatchewan","funders":"","keywords":"Biology; Dynamin; Missense mutation; Genetics; Locus (genetics); Mutation; Point mutation; Haplotype; Gene; Endocytosis; Genotype; Cell","score_opus":0.006780331938704137,"score_gpt":0.2097229123919978,"score_spread":0.20294258045329366,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2020372995","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9966068,0.0002310053,0.0014239509,0.00015559523,0.000042065658,0.00001701116,0.00017825478,0.000055526147,0.0012897971],"genre_scores_gemma":[0.999091,0.0000568147,0.00037074045,0.000029417706,0.000023811644,0.000005292559,0.000100992256,0.0000123721475,0.0003095191],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9997173,0.000047291072,0.00003215408,0.00008025073,0.000083030565,0.000039906106],"domain_scores_gemma":[0.99927586,0.00030332673,0.0002101211,0.000027316903,0.00002757409,0.00015579829],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00018956588,0.0010950889,0.0005591284,0.0013024409,0.00045452474,0.00027787674,0.0005024217,0.0013304581,0.0019831539],"category_scores_gemma":[0.0010211251,0.00026610543,0.00037499488,0.0006224316,0.0010517611,0.0002672256,0.0007264024,0.00061408145,0.00028684258],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0016448329,0.00020264732,0.039607447,0.0002704421,0.00016761558,0.40265936,0.0005264085,0.0011132899,0.54165345,0.002098418,0.0010956731,0.0089604305],"study_design_scores_gemma":[0.00015928614,0.0007782188,0.2789709,0.00007206142,0.00019624337,0.6579308,0.00027408707,0.005139405,0.05138448,0.00143249,0.003543463,0.000118626915],"about_ca_topic_score_codex":0.00074724463,"about_ca_topic_score_gemma":0.0009107843,"teacher_disagreement_score":0.0019831539,"about_ca_system_score_codex":0.00021597618,"about_ca_system_score_gemma":0.00017934422,"threshold_uncertainty_score":0.0066343546},"labels":[],"label_agreement":null},{"id":"W2020725656","doi":"10.1038/ng.1091","title":"De novo mutations in the actin genes ACTB and ACTG1 cause Baraitser-Winter syndrome","year":2012,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Hedgehog Signaling Pathway Studies","field":"Biochemistry, Genetics and Molecular Biology","cited_by":306,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Western University; McMaster University","funders":"National Institute of Neurological Disorders and Stroke; National Institute of Environmental Health Sciences; Canadian Institutes of Health Research; National Heart, Lung, and Blood Institute; University of Washington","keywords":"Biology; Missense mutation; Proband; Genetics; Exome sequencing; Phenotype; Gene; Exome; Mutation; Lissencephaly","score_opus":0.01592370567046873,"score_gpt":0.28941977380676226,"score_spread":0.2734960681362935,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2020725656","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9925363,0.0008147186,0.0029393828,0.00031466957,0.000091075366,0.000018007668,0.00022943011,0.00014871963,0.0029077088],"genre_scores_gemma":[0.9967014,0.0003255804,0.0014746784,0.00005976738,0.000047072164,0.000009502643,0.00012645154,0.000044079497,0.0012114287],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9997379,0.000027031288,0.000024826177,0.000057099307,0.00012107076,0.00003212311],"domain_scores_gemma":[0.99960774,0.00011068826,0.0001252817,0.00002265965,0.000016789383,0.00011688178],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00015124255,0.0014000003,0.0003811271,0.0012959575,0.00038931853,0.00037182952,0.00046216525,0.001586978,0.0020548657],"category_scores_gemma":[0.0005582641,0.0003942365,0.00028523008,0.0005449137,0.00090937084,0.0003435025,0.0005199465,0.0008431359,0.00055443944],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00039401033,0.000109199646,0.020189092,0.00009051605,0.00015493899,0.1739216,0.00035037706,0.0011335929,0.78798175,0.0030838123,0.00083547726,0.011755626],"study_design_scores_gemma":[0.00023716653,0.00036028842,0.20946291,0.000054669435,0.00043165276,0.51350486,0.0005027763,0.0057904953,0.25357482,0.003789627,0.012186926,0.00010383295],"about_ca_topic_score_codex":0.0008900605,"about_ca_topic_score_gemma":0.0014458927,"teacher_disagreement_score":0.0020548657,"about_ca_system_score_codex":0.0003109189,"about_ca_system_score_gemma":0.00024075096,"threshold_uncertainty_score":0.0068742037},"labels":[],"label_agreement":null},{"id":"W2020906240","doi":"10.1038/ng.689","title":"Genome-wide association study identifies a psoriasis susceptibility locus at TRAF3IP2","year":2010,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Psoriasis: Treatment and Pathogenesis","field":"Immunology and Microbiology","cited_by":362,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Toronto; University Health Network; Memorial University of Newfoundland","funders":"National Institute of Arthritis and Musculoskeletal and Skin Diseases","keywords":"Single-nucleotide polymorphism; Psoriasis; Biology; Genome-wide association study; Locus (genetics); Genetics; Psoriatic arthritis; Genetic association; Disease; SNP; Genotype; Gene; Immunology; Internal medicine; Medicine","score_opus":0.008799259409241606,"score_gpt":0.24551446979487454,"score_spread":0.23671521038563292,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2020906240","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9963193,0.0005478945,0.0012692352,0.0002779278,0.000035184046,0.000014040419,0.000565814,0.000057642512,0.00091297773],"genre_scores_gemma":[0.9985605,0.00012916182,0.00046238618,0.00006545172,0.000033797853,0.0000068226645,0.00027403206,0.000016866363,0.00045098568],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.999488,0.00013902795,0.00004922915,0.00016288493,0.000095479176,0.00006537458],"domain_scores_gemma":[0.99917126,0.00025788372,0.00022993243,0.00008542834,0.0000776665,0.00017796918],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00067352003,0.0007678757,0.0004908595,0.0014097475,0.0007466613,0.0006430562,0.00055506313,0.00091174373,0.0030809522],"category_scores_gemma":[0.00094795,0.0003276427,0.000958211,0.0014981884,0.00045745546,0.00019433783,0.00038169432,0.0010078778,0.00036423153],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.015205011,0.00060370425,0.52914244,0.0001909473,0.0030722362,0.008379198,0.0004378176,0.0005946678,0.42285362,0.0008686279,0.0024461227,0.016205702],"study_design_scores_gemma":[0.00037604276,0.00031617784,0.9811338,0.000019302262,0.0014350628,0.00579311,0.00018972036,0.0011867377,0.007873705,0.00045404016,0.0011869584,0.000035404613],"about_ca_topic_score_codex":0.0034705373,"about_ca_topic_score_gemma":0.003382505,"teacher_disagreement_score":0.0034705373,"about_ca_system_score_codex":0.00026870743,"about_ca_system_score_gemma":0.0002986638,"threshold_uncertainty_score":0.010306835},"labels":[],"label_agreement":null},{"id":"W2021354108","doi":"10.1038/73417","title":"Basal cell carcinomas in mice overexpressing Gli2 in skin","year":2000,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Hedgehog Signaling Pathway Studies","field":"Biochemistry, Genetics and Molecular Biology","cited_by":400,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"SickKids Foundation; University of Toronto; Hospital for Sick Children","funders":"National Cancer Institute","keywords":"GLI2; Biology; Hedgehog signaling pathway; Transcription factor; Cancer research; Hedgehog; Sonic hedgehog; Effector; Skin cancer; Basal cell carcinoma; Oncogene; Basal (medicine); Cancer; Cell biology; Signal transduction; Endocrinology; Internal medicine; Basal cell; Genetics; Gene; Cell cycle; Medicine","score_opus":0.006347718748849174,"score_gpt":0.23862701505653866,"score_spread":0.23227929630768948,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2021354108","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9698346,0.0029828935,0.007234723,0.0005883838,0.0002319228,0.00030660618,0.00376744,0.001133961,0.013919477],"genre_scores_gemma":[0.9690196,0.0013707366,0.0027205683,0.00023298878,0.000056596942,0.0001898658,0.0012039714,0.0004846391,0.024721062],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99923885,0.00008766438,0.00005938354,0.00020924327,0.00023834653,0.0001664084],"domain_scores_gemma":[0.9989699,0.00015472552,0.00026598497,0.00014493246,0.00006822635,0.00039614076],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00034025352,0.0015325345,0.0007792588,0.0035026746,0.0009778664,0.0012588516,0.00067359454,0.0012848679,0.008603972],"category_scores_gemma":[0.00028116393,0.0014645305,0.0010356703,0.000827633,0.0011757705,0.0011143485,0.00071939896,0.0031359522,0.0023129915],"study_design_candidate":"bench_or_experimental","study_design_consensus":"bench_or_experimental","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00047199885,0.000112595575,0.00034534343,0.000036300513,0.00002045075,0.0004646725,0.000049282284,0.00011874941,0.9968104,0.0006892248,0.0001277833,0.00075330026],"study_design_scores_gemma":[0.00009284091,0.00022551771,0.005305346,0.000012812455,0.00007617755,0.0024367496,0.00009953036,0.0005259728,0.98929846,0.00029159817,0.0016196145,0.000015342326],"about_ca_topic_score_codex":0.002577022,"about_ca_topic_score_gemma":0.002903674,"teacher_disagreement_score":0.008603972,"about_ca_system_score_codex":0.0008616212,"about_ca_system_score_gemma":0.000612458,"threshold_uncertainty_score":0.028783143},"labels":[],"label_agreement":null},{"id":"W2021654829","doi":"10.1038/ng.403","title":"The 8q24 cancer risk variant rs6983267 shows long-range interaction with MYC in colorectal cancer","year":2009,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Genetic factors in colorectal cancer","field":"Medicine","cited_by":666,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Calgary","funders":"National Cancer Institute; Howard Hughes Medical Institute","keywords":"Biology; TCF7L2; Genetics; Enhancer; TCF4; Transcription factor; Oncogene; Colorectal cancer; Allele; Cancer; Gene; Genotype; Single-nucleotide polymorphism; Cell cycle","score_opus":0.008948262471247014,"score_gpt":0.2948437457311811,"score_spread":0.2858954832599341,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2021654829","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99766016,0.0005801642,0.00042319612,0.00029525653,0.000037716643,0.0000037582734,0.0002933617,0.00002922432,0.00067719765],"genre_scores_gemma":[0.99914646,0.00005881424,0.00022410667,0.00006198139,0.000040647847,0.000004024275,0.00013361718,0.000014230387,0.00031624906],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99932504,0.000255925,0.000077603814,0.00014658266,0.000114323215,0.00008060136],"domain_scores_gemma":[0.99779713,0.0010101284,0.000627325,0.00011767353,0.00012473793,0.00032293677],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00039981923,0.00065964385,0.00072085764,0.0010956607,0.0005438293,0.00043419134,0.0005972494,0.0010696974,0.005211239],"category_scores_gemma":[0.002059994,0.00026010783,0.0006344401,0.0011384973,0.0003818421,0.00023116433,0.00033338362,0.0007988803,0.0005704462],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.010749927,0.00039237266,0.5204215,0.00022558222,0.0023505993,0.020999402,0.0005155087,0.0018493427,0.41375092,0.0011260313,0.0030094932,0.024609333],"study_design_scores_gemma":[0.0002983829,0.0008236416,0.95959556,0.00003466275,0.0009822808,0.016485702,0.0002274051,0.0026185263,0.014868196,0.0012151083,0.0027855597,0.00006495573],"about_ca_topic_score_codex":0.001760546,"about_ca_topic_score_gemma":0.0025088498,"teacher_disagreement_score":0.005211239,"about_ca_system_score_codex":0.00018330241,"about_ca_system_score_gemma":0.0001619193,"threshold_uncertainty_score":0.017433286},"labels":[],"label_agreement":null},{"id":"W2022051629","doi":"10.1038/ng1487","title":"Deletion of the NESP55 differentially methylated region causes loss of maternal GNAS imprints and pseudohypoparathyroidism type Ib","year":2004,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":252,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Children's Hospital of Eastern Ontario","funders":"Division of Materials Research; National Institute of Diabetes and Digestive and Kidney Diseases","keywords":"GNAS complex locus; Pseudohypoparathyroidism; Biology; Genomic imprinting; Genetics; Exon; Imprinting (psychology); Epigenetics; Allele; Gene; Internal medicine; DNA methylation; Parathyroid hormone; Gene expression; Medicine","score_opus":0.007878920898433147,"score_gpt":0.24176156477481606,"score_spread":0.2338826438763829,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2022051629","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9973115,0.00013876158,0.0010418479,0.00009264438,0.000028609056,0.000012200268,0.00037136418,0.000060080354,0.00094302587],"genre_scores_gemma":[0.99811137,0.00008342577,0.0005008708,0.000034904093,0.000007167926,0.000009220878,0.00023725143,0.000026555485,0.0009892017],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99974936,0.00002971361,0.000045029192,0.000057675486,0.00005956916,0.00005865922],"domain_scores_gemma":[0.9995988,0.0001323873,0.00011824,0.000043940054,0.00000963008,0.000097020886],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0001191235,0.0005149485,0.00028679392,0.00050878926,0.00023822441,0.0002754813,0.00057782873,0.0006128547,0.0031052139],"category_scores_gemma":[0.00038067266,0.00029729732,0.0004024958,0.00024325721,0.000625883,0.00012946123,0.00045724708,0.00057535013,0.00039921957],"study_design_candidate":"bench_or_experimental","study_design_consensus":"bench_or_experimental","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00056379876,0.000057450186,0.0017732057,0.00003800316,0.000041627754,0.005070436,0.000047219528,0.0004315593,0.9891266,0.00054049346,0.000101450256,0.0022081428],"study_design_scores_gemma":[0.00018698358,0.00059293734,0.05202215,0.000016614993,0.00014101023,0.02709605,0.00021413254,0.0029398573,0.91246635,0.0004552973,0.0038302948,0.000038374936],"about_ca_topic_score_codex":0.0017615469,"about_ca_topic_score_gemma":0.0020859535,"teacher_disagreement_score":0.0031052139,"about_ca_system_score_codex":0.00038910797,"about_ca_system_score_gemma":0.00030780234,"threshold_uncertainty_score":0.010388017},"labels":[],"label_agreement":null},{"id":"W2022609707","doi":"10.1038/ng.589","title":"Mutations in the SHANK2 synaptic scaffolding gene in autism spectrum disorder and mental retardation","year":2010,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Autism Spectrum Disorder Research","field":"Neuroscience","cited_by":578,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"SickKids Foundation; Hospital for Sick Children; McMaster University; University of Toronto","funders":"Canadian Institutes of Health Research","keywords":"Autism spectrum disorder; Biology; Autism; Intellectual disability; Genetics; Gene; Scaffold protein; Mutation; Developmental disorder; Copy-number variation; Neurodevelopmental disorder; Psychiatry; Psychology; Genome","score_opus":0.012721772738106424,"score_gpt":0.2919961161147666,"score_spread":0.2792743433766602,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2022609707","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9929067,0.0008046728,0.0013220453,0.0005678735,0.000103439204,0.000026525158,0.00037225048,0.00012478589,0.0037717763],"genre_scores_gemma":[0.9971732,0.00019091979,0.0011520466,0.000064800086,0.000037154077,0.000011044095,0.000115584546,0.000028391525,0.0012267525],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.99972814,0.000038220216,0.00004039493,0.00007001105,0.00009171675,0.000031414962],"domain_scores_gemma":[0.99962056,0.00011979679,0.00011193722,0.000021575055,0.000034847963,0.00009138585],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00023790346,0.0019683263,0.00047923764,0.0014206194,0.00074434595,0.00045412823,0.0007344017,0.0015705551,0.003054076],"category_scores_gemma":[0.0010502627,0.00038136536,0.0006104314,0.00061670376,0.0013418103,0.00037897716,0.0008898349,0.0006751135,0.00043658278],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0035371615,0.00030536306,0.040296186,0.00035723211,0.00079024036,0.40091988,0.0011961219,0.005784782,0.50878716,0.0066344016,0.004604203,0.026787294],"study_design_scores_gemma":[0.0009000388,0.0007772335,0.2044818,0.00017731385,0.0010345757,0.6165884,0.0010517207,0.010196621,0.148385,0.0058736484,0.010280379,0.00025331715],"about_ca_topic_score_codex":0.005160666,"about_ca_topic_score_gemma":0.0053796,"teacher_disagreement_score":0.005160666,"about_ca_system_score_codex":0.0007660704,"about_ca_system_score_gemma":0.0006253186,"threshold_uncertainty_score":0.010261238},"labels":[],"label_agreement":null},{"id":"W2023013441","doi":"10.1038/ng.2637","title":"Genome-wide association study of multiple congenital heart disease phenotypes identifies a susceptibility locus for atrial septal defect at chromosome 4p16","year":2013,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Congenital heart defects research","field":"Biochemistry, Genetics and Molecular Biology","cited_by":165,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Hospital for Sick Children","funders":"National Heart, Lung, and Blood Institute; National Institute for Health and Care Research; British Heart Foundation; Wellcome Trust","keywords":"Genome-wide association study; Odds ratio; Biology; Genetics; Cohort; Locus (genetics); Population; Internal medicine; Genotype; Medicine; Single-nucleotide polymorphism; Gene","score_opus":0.009900601675914052,"score_gpt":0.28034665167914097,"score_spread":0.2704460500032269,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2023013441","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9980757,0.0003828018,0.0007478923,0.00011603744,0.00002591428,0.000007554817,0.00025727367,0.000032633678,0.00035420738],"genre_scores_gemma":[0.99811953,0.00018918049,0.00081403746,0.000029795823,0.000027568987,0.000012269043,0.00034449273,0.000015233231,0.00044768432],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99933124,0.0001926158,0.00006264637,0.00019273818,0.00014649288,0.00007422369],"domain_scores_gemma":[0.9984333,0.00061669893,0.00047896503,0.00012614085,0.00007185465,0.00027307606],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0007201054,0.0010230313,0.0007897832,0.0022062967,0.0006238879,0.0005956866,0.0008279281,0.00089234306,0.0034922413],"category_scores_gemma":[0.0016486415,0.0005495465,0.0010526994,0.0014673106,0.00069943815,0.00021178073,0.000862254,0.0010113404,0.00025656453],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0049117305,0.0002988853,0.79465395,0.0001077773,0.002341235,0.0065454207,0.00033987925,0.00078681164,0.17662011,0.00051826437,0.00091874326,0.011957135],"study_design_scores_gemma":[0.00031908334,0.00037731708,0.97912025,0.000023158538,0.00097472494,0.007920213,0.00015427124,0.0013658066,0.008503303,0.00044000984,0.0007739559,0.000027749566],"about_ca_topic_score_codex":0.0025622977,"about_ca_topic_score_gemma":0.0033483207,"teacher_disagreement_score":0.0034922413,"about_ca_system_score_codex":0.0002476946,"about_ca_system_score_gemma":0.00043666168,"threshold_uncertainty_score":0.011682689},"labels":[],"label_agreement":null},{"id":"W2023235195","doi":"10.1038/ng.2726","title":"GRIN2A mutations in acquired epileptic aphasia and related childhood focal epilepsies and encephalopathies with speech and language dysfunction","year":2013,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Genetics and Neurodevelopmental Disorders","field":"Biochemistry, Genetics and Molecular Biology","cited_by":441,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Hospital for Sick Children; University of Toronto","funders":"Wellcome Trust","keywords":"Epilepsy; Rolandic epilepsy; Neuroscience; Aphasia; Psychology; Epilepsy syndromes; Etiology; Psychiatry","score_opus":0.002384983578797405,"score_gpt":0.1988877398168053,"score_spread":0.1965027562380079,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2023235195","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9965442,0.00049640797,0.00036384756,0.0001333765,0.000032965738,0.000018053555,0.00017939895,0.000022121641,0.0022096047],"genre_scores_gemma":[0.9992047,0.0000839796,0.0002966333,0.00004764713,0.000024221139,0.000005114894,0.000071978924,0.000008074933,0.00025763028],"study_design_codex":"case_report","study_design_gemma":"observational","domain_scores_codex":[0.9995739,0.00008115231,0.00008791426,0.000086140535,0.0000885596,0.00008236348],"domain_scores_gemma":[0.9992366,0.00025809347,0.00028560715,0.00003298792,0.000046986264,0.00013972606],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00033911713,0.0012371287,0.00046859958,0.0013013323,0.00050858944,0.00040154686,0.00060701044,0.0015069734,0.0029294214],"category_scores_gemma":[0.0015614496,0.00035191452,0.00054885447,0.00061698863,0.0010413245,0.0003983737,0.0007075149,0.0005257261,0.00040970513],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.003134267,0.00026598616,0.10726598,0.00022048608,0.0003735536,0.76744205,0.0010539589,0.001769134,0.10570732,0.0015471877,0.0012949187,0.009925178],"study_design_scores_gemma":[0.0004315935,0.00037657327,0.269118,0.000072895346,0.0004006408,0.70633334,0.00061440346,0.0029500679,0.016072188,0.0013212683,0.0022399141,0.00006918396],"about_ca_topic_score_codex":0.0024390668,"about_ca_topic_score_gemma":0.0040118704,"teacher_disagreement_score":0.0029294214,"about_ca_system_score_codex":0.00049282383,"about_ca_system_score_gemma":0.0003517666,"threshold_uncertainty_score":0.009799898},"labels":[],"label_agreement":null},{"id":"W2023630351","doi":"10.1038/ng0904-921","title":"The Knockout Mouse Project","year":2004,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Animal Genetics and Reproduction","field":"Biochemistry, Genetics and Molecular Biology","cited_by":619,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Toronto; Research Manitoba","funders":"National Center for Research Resources; National Institute of Mental Health; National Institutes of Health; GlaxoSmithKline; University of Toronto; National Institute on Deafness and Other Communication Disorders; University of Pennsylvania; Wellcome Trust","keywords":"Gene knockout; Biology; Knockout mouse; Computational biology; Function (biology); Gene; Phenotype; Laboratory mouse; Genetics; Gene targeting","score_opus":0.00672547653062129,"score_gpt":0.2619272453888906,"score_spread":0.25520176885826934,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2023630351","genre_codex":"methods","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":null,"domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.054244954,0.04211627,0.416991,0.017682059,0.009820196,0.0052349437,0.19132245,0.043912366,0.21867572],"genre_scores_gemma":[0.08953404,0.05747073,0.2970958,0.0110513335,0.0014771362,0.010477159,0.3089714,0.0072376863,0.2166847],"study_design_codex":"not_applicable","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99810624,0.00050694676,0.00017887249,0.0003051907,0.0006740538,0.00022871137],"domain_scores_gemma":[0.9983083,0.0002520047,0.00020440883,0.00033447857,0.00033555046,0.0005652013],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0038435895,0.0015332841,0.0014878382,0.002307616,0.0012143105,0.0019354406,0.0031023193,0.0017770604,0.041977443],"category_scores_gemma":[0.00215858,0.0007262134,0.0010360018,0.0011768764,0.0009561103,0.0012221425,0.0024830927,0.0030212582,0.022596534],"study_design_candidate":"bench_or_experimental","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.001721686,0.00040930577,0.0020851681,0.0015019075,0.00038590532,0.0011259511,0.00018315954,0.001371767,0.13078624,0.038584925,0.5560391,0.26580483],"study_design_scores_gemma":[0.000509865,0.00047396193,0.0025403504,0.00039432055,0.00028399407,0.0028702116,0.000031236294,0.0008732056,0.022212842,0.0073596667,0.96237344,0.00007698773],"about_ca_topic_score_codex":0.0016242486,"about_ca_topic_score_gemma":0.0023266785,"teacher_disagreement_score":0.041977443,"about_ca_system_score_codex":0.00079685025,"about_ca_system_score_gemma":0.003266594,"threshold_uncertainty_score":0.14042848},"labels":[],"label_agreement":null},{"id":"W2024201682","doi":"10.1038/ng.422","title":"FOXC1 is required for normal cerebellar development and is a major contributor to chromosome 6p25.3 Dandy-Walker malformation","year":2009,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Fetal and Pediatric Neurological Disorders","field":"Medicine","cited_by":282,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Alberta","funders":"National Institute of Neurological Disorders and Stroke; Eunice Kennedy Shriver National Institute of Child Health and Human Development; National Cancer Institute","keywords":"Biology; Hindbrain; Fourth ventricle; Anatomy; Cerebellar vermis; Hypoplasia; Brachyury; Locus (genetics); Cerebellum; Genetics; Mesoderm; Neuroscience; Embryo; Embryonic stem cell","score_opus":0.010727533404131613,"score_gpt":0.2583265379056859,"score_spread":0.24759900450155428,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2024201682","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.98464036,0.0034291546,0.0042045624,0.0005939774,0.000105046056,0.000033423563,0.0016591506,0.00024441464,0.0050899056],"genre_scores_gemma":[0.99342316,0.00061296736,0.00150752,0.00007817511,0.000021240136,0.000014015515,0.00087017013,0.000061256964,0.0034114968],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9997993,0.000014491237,0.000013512009,0.00004763163,0.00009240591,0.000032690066],"domain_scores_gemma":[0.9997185,0.000046030804,0.00009872564,0.000020756874,0.000029879779,0.00008614847],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00014417006,0.0003647592,0.0003048916,0.00083072355,0.00043840546,0.00033768456,0.0004629236,0.0005646368,0.0029922498],"category_scores_gemma":[0.0005443077,0.00024618427,0.0001798079,0.0003631055,0.00051024696,0.00014932151,0.00033132854,0.00049816445,0.00060372724],"study_design_candidate":"bench_or_experimental","study_design_consensus":"bench_or_experimental","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00045561866,0.000042253992,0.015783397,0.00015633972,0.00006429277,0.0079751965,0.000121907025,0.0007744708,0.95165485,0.0018584401,0.0020414002,0.019071836],"study_design_scores_gemma":[0.00017205425,0.0002563041,0.27349836,0.00009326974,0.0002393715,0.038468186,0.00024366798,0.0047426913,0.6379027,0.0022649118,0.04204597,0.00007252177],"about_ca_topic_score_codex":0.0067975447,"about_ca_topic_score_gemma":0.0076849344,"teacher_disagreement_score":0.0067975447,"about_ca_system_score_codex":0.000643355,"about_ca_system_score_gemma":0.0005258604,"threshold_uncertainty_score":0.013515949},"labels":[],"label_agreement":null},{"id":"W2024373518","doi":"10.1038/ng.518","title":"Somatic mutations altering EZH2 (Tyr641) in follicular and diffuse large B-cell lymphomas of germinal-center origin","year":2010,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Epigenetics and DNA Methylation","field":"Biochemistry, Genetics and Molecular Biology","cited_by":1650,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of British Columbia; BC Cancer Agency","funders":"National Cancer Institute; Canadian Institutes of Health Research","keywords":"EZH2; Histone H3; Biology; PRC2; Histone methyltransferase; Germinal center; Cancer research; Diffuse large B-cell lymphoma; Histone methylation; Histone; Molecular biology; B cell; Genetics; DNA methylation; Gene; Gene expression; Antibody","score_opus":0.004996011660939228,"score_gpt":0.26184151225448365,"score_spread":0.25684550059354444,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2024373518","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99924314,0.00011150125,0.00015345494,0.000019071103,0.000004329991,0.0000043363716,0.000057200024,0.000008895849,0.00039818505],"genre_scores_gemma":[0.9995672,0.000045211204,0.000089734865,0.0000060730126,0.0000039149368,0.0000026807231,0.000043427302,0.0000038956487,0.00023770286],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9998746,0.000017911192,0.000018671804,0.000025966385,0.00003265205,0.00003016839],"domain_scores_gemma":[0.9998387,0.000043355132,0.00004973535,0.000011031865,0.000009381768,0.00004770215],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00014707175,0.00025542692,0.00021638308,0.0005945717,0.00021176598,0.00026853636,0.00021562065,0.00046994217,0.0016866649],"category_scores_gemma":[0.0004046531,0.00018274834,0.00017018968,0.0002790587,0.0003627655,0.0001643739,0.000307729,0.00023678715,0.00022513003],"study_design_candidate":"bench_or_experimental","study_design_consensus":"bench_or_experimental","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0028541873,0.00010784592,0.033287946,0.00006226679,0.00010167406,0.008582198,0.00014598345,0.00045579582,0.94466573,0.00037402744,0.00021297504,0.009149374],"study_design_scores_gemma":[0.00076503516,0.0012915055,0.42920467,0.000017846756,0.0005127068,0.10695427,0.0004945158,0.0038414528,0.45187995,0.0011664776,0.0038154353,0.00005608621],"about_ca_topic_score_codex":0.0007212372,"about_ca_topic_score_gemma":0.00096124085,"teacher_disagreement_score":0.0016866649,"about_ca_system_score_codex":0.0002505238,"about_ca_system_score_gemma":0.00013548977,"threshold_uncertainty_score":0.0056424737},"labels":[],"label_agreement":null},{"id":"W2024642024","doi":"10.1038/ng1770","title":"Magnitude and distribution of linkage disequilibrium in population isolates and implications for genome-wide association studies","year":2006,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Genetic Associations and Epidemiology","field":"Biochemistry, Genetics and Molecular Biology","cited_by":280,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Memorial University of Newfoundland","funders":"National Eye Institute; Wellcome Trust","keywords":"Biology; Linkage disequilibrium; Genetics; Genome-wide association study; Genetic association; Linkage (software); Genome; Population; Association mapping; Tag SNP; Population genetics; Evolutionary biology; Single-nucleotide polymorphism; Allele; Haplotype; Genotype; Gene; Demography","score_opus":0.008566506886951802,"score_gpt":0.2845694074575592,"score_spread":0.2760029005706074,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2024642024","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.98828864,0.0019574114,0.0073708314,0.00044485004,0.000024984365,0.000024714634,0.00053939916,0.00004020302,0.001309013],"genre_scores_gemma":[0.9982192,0.00022409712,0.0011014061,0.00005361114,0.000035585195,0.000012763343,0.00021744239,0.000010105816,0.00012577891],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.98309946,0.0108588515,0.0012440839,0.0029707719,0.0012302613,0.00059646217],"domain_scores_gemma":[0.95202434,0.036827926,0.0038328632,0.004439695,0.0018737263,0.0010014897],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.015765276,0.00036421054,0.0012006419,0.0039637685,0.0011157623,0.0022237,0.0013667074,0.0013499999,0.0026545564],"category_scores_gemma":[0.0464534,0.0005800289,0.0007059285,0.0039108503,0.0023502558,0.0013417184,0.0014841364,0.0015718994,0.00034485318],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0016971977,0.00012499167,0.9691087,0.00011501437,0.0012671814,0.0003446151,0.0013215998,0.0011213314,0.008070842,0.0028792722,0.0002926407,0.013656557],"study_design_scores_gemma":[0.0001141275,0.00021593124,0.9857416,0.000023605686,0.0005193086,0.0010570425,0.00078411686,0.0029806853,0.0006961181,0.006971054,0.0008490652,0.000047455334],"about_ca_topic_score_codex":0.0020064132,"about_ca_topic_score_gemma":0.0017247349,"teacher_disagreement_score":0.015765276,"about_ca_system_score_codex":0.0004758042,"about_ca_system_score_gemma":0.00033998583,"threshold_uncertainty_score":0.08337575},"labels":[],"label_agreement":null},{"id":"W2025291304","doi":"10.1038/87374","title":"Monocytic leukemia zinc-finger protein MOZ and its related factor MORF are new histone acetyltransferases","year":2001,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Cancer-related gene regulation","field":"Biochemistry, Genetics and Molecular Biology","cited_by":1,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"McGill University Health Centre","funders":"","keywords":"Histone Acetyltransferases; Biology; Zinc finger; Acetyltransferases; Histone; Genetics; Cancer research; Computational biology; Acetylation; Transcription factor; Gene","score_opus":0.009784835614017178,"score_gpt":0.25873631035728684,"score_spread":0.24895147474326965,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2025291304","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9546653,0.01715018,0.022800976,0.0005522146,0.0001471864,0.00003041247,0.0005736792,0.00050665654,0.0035734335],"genre_scores_gemma":[0.9764815,0.0052917264,0.010306019,0.00018046342,0.000070157934,0.00002795948,0.0009975019,0.000042220174,0.006602262],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9999043,0.0000059893855,0.0000033966255,0.000017914645,0.00004186402,0.000026588577],"domain_scores_gemma":[0.9999105,0.000009783083,0.000025733509,0.000009409377,0.00001171495,0.00003294827],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00013494631,0.00023641491,0.00025916912,0.00023539737,0.0002767148,0.00046631348,0.00027521324,0.00025327635,0.00060242217],"category_scores_gemma":[0.00016883071,0.00017206484,0.00018821385,0.00018341046,0.00028358254,0.0002960553,0.00033882807,0.00048303916,0.00039762986],"study_design_candidate":"bench_or_experimental","study_design_consensus":"bench_or_experimental","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00034981352,0.000016554652,0.001992103,0.000037227583,0.000014353005,0.00022562267,0.000030257412,0.00013912783,0.98127204,0.0024131092,0.00036285564,0.013146857],"study_design_scores_gemma":[0.0000652398,0.00021085168,0.02890985,0.000009905145,0.000051534713,0.0025246332,0.00008802314,0.0016885645,0.9062784,0.0014138812,0.05873903,0.000020109755],"about_ca_topic_score_codex":0.0007874419,"about_ca_topic_score_gemma":0.0023472446,"teacher_disagreement_score":0.0007874419,"about_ca_system_score_codex":0.0005953946,"about_ca_system_score_gemma":0.00018870083,"threshold_uncertainty_score":0.0043199062},"labels":[],"label_agreement":null},{"id":"W2026035216","doi":"10.1038/ng.256","title":"Epithelial Pten is dispensable for intestinal homeostasis but suppresses adenoma development and progression after Apc mutation","year":2008,"lang":"en","type":"article","venue":"Nature Genetics","topic":"PI3K/AKT/mTOR signaling in cancer","field":"Biochemistry, Genetics and Molecular Biology","cited_by":108,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University Health Network","funders":"Schweizerischer Nationalfonds zur Förderung der Wissenschaftlichen Forschung; Cancer Research UK; Parc Geneteg Cymru","keywords":"PTEN; Biology; Intestinal epithelium; Cancer research; Wnt signaling pathway; Epithelium; Protein kinase B; Context (archaeology); Carcinogenesis; Stem cell; Cell biology; PI3K/AKT/mTOR pathway; Cancer; Signal transduction; Genetics","score_opus":0.012637212823779715,"score_gpt":0.27897278515079255,"score_spread":0.2663355723270128,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2026035216","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9905757,0.001194661,0.0027909572,0.00033902648,0.0000812065,0.000026911885,0.0006698706,0.000498588,0.0038229753],"genre_scores_gemma":[0.99566025,0.00039798152,0.0004691623,0.000047761176,0.000013160416,0.00001526178,0.0003884734,0.00007770909,0.0029300952],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99948454,0.000076193915,0.000051842824,0.00006763172,0.00017038987,0.0001494306],"domain_scores_gemma":[0.9992311,0.00013677822,0.00019985123,0.00007913309,0.000044627803,0.00030847182],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00025101658,0.00062518637,0.0004742318,0.0014247735,0.0003605914,0.00071997853,0.0004787995,0.00051088596,0.0031935573],"category_scores_gemma":[0.00042362662,0.00057005783,0.0004652805,0.0005172451,0.0008224843,0.00038031937,0.0006723996,0.0010326294,0.0009467333],"study_design_candidate":"bench_or_experimental","study_design_consensus":"bench_or_experimental","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0002763076,0.000034684035,0.000418062,0.000024315314,0.000009085501,0.0005632502,0.000010380027,0.000082249484,0.9973968,0.00033803686,0.000074437645,0.0007724588],"study_design_scores_gemma":[0.000044723594,0.00021833416,0.007983301,0.0000043229584,0.000039552724,0.0022398497,0.00005557688,0.0011025369,0.9851686,0.00023862583,0.0028934248,0.000011116012],"about_ca_topic_score_codex":0.0012866944,"about_ca_topic_score_gemma":0.0015791773,"teacher_disagreement_score":0.0031935573,"about_ca_system_score_codex":0.00041274284,"about_ca_system_score_gemma":0.0005592784,"threshold_uncertainty_score":0.0106835365},"labels":[],"label_agreement":null},{"id":"W2026050615","doi":"10.1038/ng.3144","title":"A recurrent de novo mutation in KCNC1 causes progressive myoclonus epilepsy","year":2014,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Glycogen Storage Diseases and Myoclonus","field":"Medicine","cited_by":315,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Toronto; McGill University; Toronto Western Hospital; Montreal Neurological Institute and Hospital","funders":"Wellcome Trust","keywords":"Biology; Progressive myoclonus epilepsy; Epilepsy; Mutation; Genetics; Myoclonus; Neuroscience; Gene","score_opus":0.008198701740935345,"score_gpt":0.2952176829423749,"score_spread":0.28701898120143954,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2026050615","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9950566,0.00036930485,0.00079425855,0.0006774212,0.00017776259,0.000042747484,0.00028468645,0.00008968692,0.0025073793],"genre_scores_gemma":[0.9982279,0.0001049148,0.00042465355,0.00018321526,0.00013328533,0.000007938912,0.00012530207,0.00002965767,0.00076317816],"study_design_codex":"case_report","study_design_gemma":"observational","domain_scores_codex":[0.9995419,0.0000476314,0.00009077604,0.00012226102,0.00010824869,0.00008921643],"domain_scores_gemma":[0.99850464,0.00055811944,0.00038996403,0.00010255031,0.00011827819,0.0003264386],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.000261615,0.0014785378,0.0006047915,0.0012493154,0.0008381192,0.00050133624,0.0010557832,0.0034489136,0.0022892023],"category_scores_gemma":[0.002040037,0.00036414873,0.0008872164,0.000818479,0.0010199195,0.000500802,0.00082324096,0.0012214199,0.00097638014],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00056153635,0.00014166551,0.016522117,0.00008791347,0.0001165461,0.90774953,0.00040114048,0.00052360666,0.06674035,0.0005591561,0.0012565205,0.005339914],"study_design_scores_gemma":[0.0001608775,0.00056345196,0.064055,0.000040247156,0.00020064651,0.9135501,0.00031161305,0.0022006435,0.01590746,0.0004793763,0.0024304327,0.00010005786],"about_ca_topic_score_codex":0.0025580563,"about_ca_topic_score_gemma":0.0031693908,"teacher_disagreement_score":0.0034489136,"about_ca_system_score_codex":0.0007456651,"about_ca_system_score_gemma":0.00047393265,"threshold_uncertainty_score":0.0076581836},"labels":[],"label_agreement":null},{"id":"W2026615227","doi":"10.1038/ng.395","title":"REL, encoding a member of the NF-κB family of transcription factors, is a newly defined risk locus for rheumatoid arthritis","year":2009,"lang":"en","type":"article","venue":"Nature Genetics","topic":"NF-κB Signaling Pathways","field":"Biochemistry, Genetics and Molecular Biology","cited_by":330,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Toronto; University Health Network; Mount Sinai Hospital","funders":"National Institute of Arthritis and Musculoskeletal and Skin Diseases; National Institutes of Health","keywords":"Rheumatoid arthritis; Locus (genetics); Biology; Allele; Genome-wide association study; Gene; Genetics; Genetic association; Immune system; Immunology; Arthritis; Single-nucleotide polymorphism; Genotype","score_opus":0.011920521939783213,"score_gpt":0.23973546634866913,"score_spread":0.22781494440888592,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2026615227","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.95858455,0.006597582,0.024826553,0.0009179283,0.00022905025,0.00009544894,0.0018847577,0.00053978025,0.006324377],"genre_scores_gemma":[0.97867316,0.0028867126,0.011515349,0.0003072164,0.00021006679,0.000049262606,0.0016813991,0.00009089947,0.004585876],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.99969125,0.000042249725,0.000017216234,0.00010607085,0.0001051176,0.00003815267],"domain_scores_gemma":[0.99956936,0.00009527374,0.00017656952,0.000024047977,0.000038826405,0.00009588116],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00019230101,0.0007728979,0.00062409753,0.0008677164,0.00029911002,0.00040322565,0.00039884946,0.00060666865,0.0024380055],"category_scores_gemma":[0.00049313396,0.00024264593,0.00045389734,0.00047210522,0.00044587458,0.00017005893,0.00037993182,0.0008935989,0.00081803766],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0014732423,0.00014158685,0.023594012,0.00021396844,0.000095002,0.0048846533,0.00014714224,0.00018214509,0.9454468,0.0018413018,0.0006840884,0.021296056],"study_design_scores_gemma":[0.0011040769,0.0027545397,0.421434,0.00027915806,0.0011643468,0.12138846,0.0007877023,0.0037367092,0.37654725,0.0076780114,0.06286819,0.0002576379],"about_ca_topic_score_codex":0.0008333804,"about_ca_topic_score_gemma":0.0006664644,"teacher_disagreement_score":0.0024380055,"about_ca_system_score_codex":0.00028312925,"about_ca_system_score_gemma":0.00029095393,"threshold_uncertainty_score":0.008155942},"labels":[],"label_agreement":null},{"id":"W2026813804","doi":"10.1038/ng0505-457","title":"Universal epistasis analysis","year":2005,"lang":"en","type":"letter","venue":"Nature Genetics","topic":"Molecular Biology Techniques and Applications","field":"Biochemistry, Genetics and Molecular Biology","cited_by":9,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Toronto","funders":"","keywords":"Epistasis; Biology; Multicellular organism; Phenotype; Computational biology; Genetics; Microarray analysis techniques; Genetic analysis; Evolutionary biology; Gene; Gene expression","score_opus":0.004998081804888688,"score_gpt":0.26066431753250474,"score_spread":0.25566623572761604,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2026813804","genre_codex":"methods","genre_gemma":"commentary","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"commentary","genre_consensus":null,"domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.022485746,0.00394454,0.9170811,0.011190584,0.002967804,0.000080622114,0.0005677914,0.0025347886,0.039147053],"genre_scores_gemma":[0.67957085,0.0024363708,0.27572882,0.0077407253,0.0018483758,0.00019056669,0.00085220154,0.0009779441,0.030654136],"study_design_codex":"theoretical_or_conceptual","study_design_gemma":"theoretical_or_conceptual","domain_scores_codex":[0.9987999,0.00042643605,0.000044758806,0.00032577186,0.00027705752,0.00012603444],"domain_scores_gemma":[0.9988361,0.00045551016,0.000056725014,0.00043339195,0.00013972056,0.0000786108],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0014901281,0.00054265594,0.0010518183,0.0010093388,0.0006427471,0.0007615903,0.0012178661,0.0008916385,0.0068189153],"category_scores_gemma":[0.0035383266,0.00029133004,0.00072391453,0.00095976476,0.0012292366,0.0016008279,0.0017494113,0.0024986286,0.0012893411],"study_design_candidate":"theoretical_or_conceptual","study_design_consensus":"theoretical_or_conceptual","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00027369172,0.00004031578,0.0013645841,0.0002242774,0.00013186903,0.00062585174,0.000109212684,0.0024283694,0.018553551,0.6784484,0.08944313,0.20835681],"study_design_scores_gemma":[0.00006808017,0.000053973796,0.0020607563,0.000042397784,0.00008433647,0.0021431562,0.00005482224,0.057350185,0.019543052,0.83152753,0.08700861,0.00006306855],"about_ca_topic_score_codex":0.00038910093,"about_ca_topic_score_gemma":0.00079407485,"teacher_disagreement_score":0.0068189153,"about_ca_system_score_codex":0.00070038566,"about_ca_system_score_gemma":0.00034225118,"threshold_uncertainty_score":0.022811532},"labels":[],"label_agreement":null},{"id":"W2026853694","doi":"10.1038/ng.2667","title":"Identification of multiple risk variants for ankylosing spondylitis through high-density genotyping of immune-related loci","year":2013,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Spondyloarthritis Studies and Treatments","field":"Medicine","cited_by":873,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Alberta; Memorial University of Newfoundland; University Health Network; Toronto Western Hospital; University of Toronto","funders":"National Health and Medical Research Council; National Institutes of Health; National Institute of Arthritis and Musculoskeletal and Skin Diseases; National Center for Research Resources; Agence Nationale de la Recherche; Versus Arthritis; National Institute of Allergy and Infectious Diseases; Medical Research Council; Vlaamse regering; Alberta Innovates; Universiteit Gent; Australian Cancer Research Foundation; Fundación para el Fomento en Asturias de la Investigación Científica Aplicada y la Tecnología; Georgia Clinical and Translational Science Alliance; National Natural Science Foundation of China; National Institute for Health and Care Research; Abbott Laboratories; Krembil Foundation; Deutsches Krebsforschungszentrum; University of Otago; Arthritis Australia; European Commission; Arthritis Society; Wellcome Trust","keywords":"Biology; Genotyping; Ankylosing spondylitis; Genetics; Identification (biology); Immune system; Computational biology; Immunology; Genotype; Gene","score_opus":0.008969090553449341,"score_gpt":0.25716801500858916,"score_spread":0.2481989244551398,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2026853694","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9890155,0.0008371604,0.008367654,0.00021429046,0.00003551164,0.000033971603,0.0003884116,0.00004309807,0.0010644052],"genre_scores_gemma":[0.9942688,0.00019093478,0.00491384,0.00009207257,0.000028086868,0.000018393872,0.00014264588,0.000011028617,0.00033429408],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9978466,0.00088612613,0.000150591,0.0006062056,0.00033217168,0.00017839162],"domain_scores_gemma":[0.99775463,0.0013318066,0.00045128315,0.000206212,0.0001459079,0.00011011575],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0015678506,0.0005800096,0.00068328745,0.0017290268,0.00047130353,0.00092519046,0.0007028215,0.0009778799,0.0010555942],"category_scores_gemma":[0.0036591755,0.00054517033,0.0006851194,0.0013054693,0.00035112732,0.00036487484,0.00058120827,0.0008705586,0.0001930086],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0010945367,0.00026739208,0.90876126,0.000102517144,0.0018836048,0.0009879384,0.0003914675,0.0019151366,0.044151668,0.00087781233,0.00065397384,0.038912535],"study_design_scores_gemma":[0.00013933716,0.00023478898,0.9827419,0.000033484444,0.0009607605,0.001629328,0.00015039711,0.006915764,0.0050849123,0.001168955,0.00090193877,0.000038332742],"about_ca_topic_score_codex":0.0033131847,"about_ca_topic_score_gemma":0.007011779,"teacher_disagreement_score":0.0033131847,"about_ca_system_score_codex":0.0002399512,"about_ca_system_score_gemma":0.00020571219,"threshold_uncertainty_score":0.008291721},"labels":[],"label_agreement":null},{"id":"W2027350554","doi":"10.1038/ng.262","title":"Meta-analysis of genome-wide association data identifies four new susceptibility loci for colorectal cancer","year":2008,"lang":"en","type":"review","venue":"Nature Genetics","topic":"Genetic factors in colorectal cancer","field":"Medicine","cited_by":564,"is_retracted":false,"has_abstract":false,"route_ca_aff":false,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"","funders":"National Cancer Institute; Medical Research Council; Bundesministerium für Bildung und Forschung; Deutsche Forschungsgemeinschaft; Ontario Genomics; National Institutes of Health; Cancer Research UK; Ontario Genomics Institute; Génome Québec; Genome Canada; Wellcome Trust; European Commission; Cancer Care Ontario","keywords":"Biology; Genome-wide association study; Colorectal cancer; Genetics; Genome; Computational biology; Genetic association; Cancer; Single-nucleotide polymorphism; Gene; Genotype","score_opus":0.17360274890601102,"score_gpt":0.40160928085755476,"score_spread":0.22800653195154374,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2027350554","genre_codex":"review","genre_gemma":"review","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"review","genre_consensus":"review","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.0018192293,0.99615854,0.000886084,0.0006456735,0.000114092756,0.0000051506595,0.00008566351,0.000018249357,0.00026731746],"genre_scores_gemma":[0.018590203,0.978118,0.0019391325,0.0005291307,0.00035272722,0.000012058445,0.0002497735,0.0000064767905,0.00020245301],"study_design_codex":"design_other","study_design_gemma":"meta_analysis","domain_scores_codex":[0.99922585,0.0002413393,0.00010340442,0.00020032303,0.00019124821,0.000037792954],"domain_scores_gemma":[0.9969903,0.002235904,0.00034646646,0.00010320111,0.0002457954,0.00007835233],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0025254893,0.0012351549,0.003988264,0.0024465793,0.00018489719,0.0009796303,0.0013914461,0.0010746205,0.0013727641],"category_scores_gemma":[0.0034162272,0.0003954549,0.002055299,0.003954359,0.00036777603,0.00062684476,0.0005311531,0.0010347265,0.00036274444],"study_design_candidate":"meta_analysis","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0010585119,0.000068962254,0.03318431,0.023331178,0.018750262,0.0012503676,0.00007201168,0.0010254568,0.0028665587,0.0012582013,0.013165682,0.9039685],"study_design_scores_gemma":[0.0014073274,0.0013309187,0.29418772,0.020236265,0.14123376,0.022140041,0.0005395835,0.0025621564,0.0060824724,0.020988353,0.4888943,0.00039708987],"about_ca_topic_score_codex":0.0016372863,"about_ca_topic_score_gemma":0.0047198855,"teacher_disagreement_score":0.003988264,"about_ca_system_score_codex":0.00048396803,"about_ca_system_score_gemma":0.0013833151,"threshold_uncertainty_score":0.013356268},"labels":[],"label_agreement":null},{"id":"W2027577263","doi":"10.1038/ng.2928","title":"Small cell carcinoma of the ovary, hypercalcemic type, displays frequent inactivating germline and somatic mutations in SMARCA4","year":2014,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Chromatin Remodeling and Cancer","field":"Biochemistry, Genetics and Molecular Biology","cited_by":385,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Canada's Michael Smith Genome Sciences Centre; University Health Network; University of British Columbia; BC Cancer Agency","funders":"National Cancer Institute","keywords":"SMARCA4; Biology; Somatic cell; Carcinogenesis; Germline mutation; Cancer research; Germline; Ovary; Ovarian cancer; Mutation; Cancer; Chromatin remodeling; Chromatin; Genetics; Gene","score_opus":0.008610111913358025,"score_gpt":0.23304550876145774,"score_spread":0.2244353968480997,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2027577263","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9974215,0.00042888164,0.000288064,0.00008509359,0.000012358661,0.000011551386,0.0002098184,0.000035487312,0.0015072733],"genre_scores_gemma":[0.99921715,0.000108339504,0.000167704,0.000012494053,0.000009377357,0.000003589883,0.0001067995,0.000006555234,0.00036777547],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9998474,0.00001352826,0.000019787358,0.00003332508,0.000047593505,0.000038427333],"domain_scores_gemma":[0.99959093,0.00012969103,0.000118005766,0.00003619439,0.00002703577,0.000098190634],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00011545017,0.0005571284,0.00035844126,0.0014611518,0.00038423052,0.00043625286,0.00041446683,0.0005471918,0.0017721335],"category_scores_gemma":[0.00069104414,0.0002987347,0.00028121888,0.0010403473,0.0005051782,0.00019834356,0.00025413095,0.00025535238,0.00030814088],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0018066794,0.00013348789,0.16162434,0.00012271496,0.0001153535,0.24417695,0.00040802537,0.00042957603,0.5798503,0.00066164316,0.00066168414,0.010009296],"study_design_scores_gemma":[0.00013865993,0.00046752568,0.47160438,0.000009722271,0.00019858226,0.43988165,0.00050727435,0.0012947943,0.081838235,0.0006735355,0.003341402,0.000044280438],"about_ca_topic_score_codex":0.0026877183,"about_ca_topic_score_gemma":0.0038323922,"teacher_disagreement_score":0.0026877183,"about_ca_system_score_codex":0.00036089064,"about_ca_system_score_gemma":0.00025119685,"threshold_uncertainty_score":0.005928397},"labels":[],"label_agreement":null},{"id":"W2027980060","doi":"10.1038/ng.163","title":"Common sequence variants on 20q11.22 confer melanoma susceptibility","year":2008,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Cutaneous Melanoma Detection and Management","field":"Medicine","cited_by":226,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Genome Canada","funders":"National Cancer Institute; National Heart, Lung, and Blood Institute","keywords":"Biology; Melanoma; Locus (genetics); Genetics; Basal cell carcinoma; Odds ratio; Allele; Genome-wide association study; Genotype; Single-nucleotide polymorphism; Internal medicine; Gene; Medicine; Basal cell","score_opus":0.026331806953295366,"score_gpt":0.2882078587250714,"score_spread":0.26187605177177603,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2027980060","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99309194,0.0011484985,0.00085930055,0.0007749674,0.000084737636,0.000031683416,0.0005447943,0.00006609596,0.0033979723],"genre_scores_gemma":[0.9978689,0.000329789,0.00057862385,0.00010379894,0.00009551442,0.000009459535,0.00022954098,0.00001691936,0.0007674305],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9993018,0.00021661916,0.00005702206,0.00019345622,0.00011614033,0.00011490522],"domain_scores_gemma":[0.9985752,0.0006102313,0.00037786594,0.00008705474,0.00009336297,0.00025635783],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0004561802,0.0012230014,0.00054438366,0.0018259847,0.0006621633,0.00062001654,0.00043337012,0.0013304695,0.010897336],"category_scores_gemma":[0.0027802587,0.00039958753,0.0006068144,0.0010631761,0.000512622,0.00026382727,0.0005634102,0.0008306254,0.0006512487],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.005577075,0.00054427196,0.573038,0.00029087474,0.0011736173,0.061609127,0.0014177853,0.0025908132,0.28496656,0.004751403,0.005780803,0.05825962],"study_design_scores_gemma":[0.00044450533,0.00081822375,0.8930651,0.0001662667,0.0010311087,0.07262505,0.0005876832,0.0026310969,0.014385831,0.006400239,0.0077474,0.000097541284],"about_ca_topic_score_codex":0.0029567555,"about_ca_topic_score_gemma":0.0032878204,"teacher_disagreement_score":0.010897336,"about_ca_system_score_codex":0.00035086265,"about_ca_system_score_gemma":0.000363497,"threshold_uncertainty_score":0.036455214},"labels":[],"label_agreement":null},{"id":"W2028368428","doi":"10.1038/ng.3089","title":"An activating NLRC4 inflammasome mutation causes autoinflammation with recurrent macrophage activation syndrome","year":2014,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Inflammasome and immune disorders","field":"Biochemistry, Genetics and Molecular Biology","cited_by":735,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Hospital for Sick Children; Alberta Children's Hospital; University of Calgary","funders":"National Institute of Arthritis and Musculoskeletal and Skin Diseases; National Institute of Allergy and Infectious Diseases; National Institutes of Health","keywords":"Inflammasome; NLRC4; Pyroptosis; AIM2; Caspase 1; Biology; Missense mutation; Innate immune system; Pyrin domain; Mutant; Mutation; Cell biology; Immunology; Inflammation; Genetics; Immune system; Gene","score_opus":0.0038312322706807074,"score_gpt":0.23664879133214756,"score_spread":0.23281755906146684,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2028368428","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9921381,0.0006780724,0.0023743487,0.0009814122,0.0001923768,0.00005750586,0.00032444383,0.00023931042,0.0030142586],"genre_scores_gemma":[0.99732864,0.00017199814,0.0011469802,0.00015749125,0.00016332422,0.000016040454,0.00009869499,0.00004590089,0.0008709686],"study_design_codex":"case_report","study_design_gemma":"observational","domain_scores_codex":[0.9991935,0.00015174683,0.00013747101,0.00019798579,0.00019191382,0.00012743243],"domain_scores_gemma":[0.9985038,0.00053600356,0.00047079532,0.00009200752,0.000092194605,0.00030515247],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00038586822,0.0023260654,0.0008594839,0.0018813135,0.0008621164,0.0006063796,0.0014300967,0.0031481017,0.0033329432],"category_scores_gemma":[0.0020211942,0.0004829634,0.0011840955,0.00094300223,0.0014843802,0.000580982,0.0011766052,0.001298661,0.00079347496],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00032718456,0.0000911833,0.007577904,0.00006621698,0.000093451374,0.9368599,0.00026287214,0.00026567973,0.050271872,0.0008378453,0.0005797315,0.0027661254],"study_design_scores_gemma":[0.00008401377,0.0002455187,0.016064417,0.000023007942,0.00017268123,0.96948224,0.00012575234,0.0009885152,0.01108207,0.00045349856,0.0012345521,0.0000437931],"about_ca_topic_score_codex":0.0010353216,"about_ca_topic_score_gemma":0.0006846449,"teacher_disagreement_score":0.0033329432,"about_ca_system_score_codex":0.0005071469,"about_ca_system_score_gemma":0.00043130163,"threshold_uncertainty_score":0.011149824},"labels":[],"label_agreement":null},{"id":"W2028785929","doi":"10.1038/ng.2682","title":"Recurrent somatic alterations of FGFR1 and NTRK2 in pilocytic astrocytoma","year":2013,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Glioma Diagnosis and Treatment","field":"Medicine","cited_by":835,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"McGill University Health Centre; Montreal Children's Hospital; University of Toronto; SickKids Foundation; Hospital for Sick Children; McGill University and Génome Québec Innovation Centre; McGill University","funders":"Heidelberger Zentrum für Personalisierte Onkologie Deutsches Krebsforschungszentrum In Der Helmholtz-Gemeinschaft; National Cancer Institute; National Institutes of Health; Deutsche Krebshilfe; Eunice Kennedy Shriver National Institute of Child Health and Human Development; Brain Tumour Charity; Bundesministerium für Bildung und Forschung; Canadian Institutes of Health Research; Genome Canada; Max-Planck-Gesellschaft; Genome British Columbia; Deutsches Krebsforschungszentrum","keywords":"Pilocytic astrocytoma; Biology; PTPN11; Cancer research; Astrocytoma; Glioma; Somatic cell; Fusion gene; MAPK/ERK pathway; Gene; Mutation; Genetics; Kinase","score_opus":0.00988872733113006,"score_gpt":0.2730605552671893,"score_spread":0.26317182793605925,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2028785929","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9965605,0.0003525019,0.0003856397,0.00013512191,0.000016945296,0.00000928067,0.0001580763,0.000045636036,0.0023361314],"genre_scores_gemma":[0.9995691,0.00005867869,0.00013820372,0.000015769841,0.0000054116067,0.0000017212021,0.000047300568,0.00000521376,0.0001586396],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99970764,0.000019980673,0.000036229387,0.000042665044,0.000115248586,0.00007824077],"domain_scores_gemma":[0.9997768,0.000037536018,0.00008387916,0.000022545175,0.00002770075,0.00005160086],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00012884533,0.0003169103,0.00023922227,0.0010074169,0.00041707855,0.0006137932,0.0003854098,0.00070348254,0.0016519859],"category_scores_gemma":[0.0008210983,0.00020071266,0.00037111237,0.000810383,0.00036313682,0.00024077207,0.00042255482,0.00025708412,0.0004438806],"study_design_candidate":"bench_or_experimental","study_design_consensus":"bench_or_experimental","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0011817383,0.00008999314,0.24286608,0.00017559086,0.00027388104,0.24507427,0.0007077773,0.0025636794,0.46351996,0.0013290381,0.0015525632,0.04066545],"study_design_scores_gemma":[0.00006915371,0.0003041464,0.49933794,0.000032064163,0.00047800623,0.40909925,0.0007925697,0.0047275093,0.07896898,0.0013640551,0.004761182,0.00006517806],"about_ca_topic_score_codex":0.003741016,"about_ca_topic_score_gemma":0.005819753,"teacher_disagreement_score":0.003741016,"about_ca_system_score_codex":0.0007608435,"about_ca_system_score_gemma":0.00035806658,"threshold_uncertainty_score":0.007438481},"labels":[],"label_agreement":null},{"id":"W2028878627","doi":"10.1038/ng.2455","title":"Exome sequencing of serous endometrial tumors identifies recurrent somatic mutations in chromatin-remodeling and ubiquitin ligase complex genes","year":2012,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Chromatin Remodeling and Cancer","field":"Biochemistry, Genetics and Molecular Biology","cited_by":435,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Canada's Michael Smith Genome Sciences Centre; University of British Columbia","funders":"National Cancer Institute; Canadian Institutes of Health Research; National Institutes of Health","keywords":"Biology; ARID1A; Exome sequencing; Serous fluid; Somatic cell; Cancer research; Chromatin remodeling; Exome; Ubiquitin ligase; Endometrial cancer; Genetics; Epigenetics; Germline mutation; Gene; Mutation; Cancer; Ubiquitin","score_opus":0.029497444196911277,"score_gpt":0.30449109463474383,"score_spread":0.2749936504378325,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2028878627","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99576867,0.00041581757,0.001533799,0.00010136174,0.0000118757125,0.000008469352,0.0013518727,0.000049105773,0.000758949],"genre_scores_gemma":[0.99587363,0.00028260026,0.0017424582,0.00007536398,0.000007370518,0.000006428637,0.00113329,0.000019682739,0.0008592624],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9998584,0.000011507369,0.000015996524,0.00003345179,0.000055096167,0.000025650628],"domain_scores_gemma":[0.9997818,0.000085918204,0.000042171392,0.000032587992,0.000022660914,0.000034896053],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00018993388,0.00028104198,0.00022676427,0.00075583835,0.0002202352,0.00041638792,0.00017181449,0.00042484555,0.0014809861],"category_scores_gemma":[0.0005638185,0.00013965006,0.00030230344,0.0004947956,0.00016563998,0.00012863075,0.00028975392,0.00024008092,0.0003021035],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0009347887,0.000051444425,0.090906754,0.00009605879,0.00021322939,0.008338656,0.00020603671,0.0007424469,0.868276,0.00036192551,0.0008155382,0.029057171],"study_design_scores_gemma":[0.00010690075,0.00027108938,0.6298364,0.000041553518,0.0004635378,0.050759915,0.00030839324,0.006124359,0.30191508,0.0007662381,0.009376205,0.000030345469],"about_ca_topic_score_codex":0.0008441818,"about_ca_topic_score_gemma":0.0022185228,"teacher_disagreement_score":0.0014809861,"about_ca_system_score_codex":0.00019105547,"about_ca_system_score_gemma":0.000111031346,"threshold_uncertainty_score":0.0049543977},"labels":[],"label_agreement":null},{"id":"W2029369364","doi":"10.1038/ng.574","title":"Substitutions in woolly mammoth hemoglobin confer biochemical properties adaptive for cold tolerance","year":2010,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Hemoglobin structure and function","field":"Biochemistry, Genetics and Molecular Biology","cited_by":123,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Manitoba","funders":"National Institute of General Medical Sciences; Mashhad University of Medical Sciences","keywords":"Biology; Globin; Hemoglobin; Evolutionary biology; Heme; Lineage (genetic); Phenotype; Adaptation (eye); Genetics; Natural selection; Selection (genetic algorithm); Gene; Biochemistry","score_opus":0.009067358671322575,"score_gpt":0.23781778260077627,"score_spread":0.2287504239294537,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2029369364","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99857044,0.000060059836,0.0007236072,0.000061237864,0.00001962313,0.0000036141316,0.000041181753,0.000024588639,0.00049556885],"genre_scores_gemma":[0.99844486,0.000051028837,0.00051364827,0.00009224299,0.00001896124,0.0000030816352,0.000086800166,0.00002959074,0.00075988454],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9998889,0.000024463423,0.000008598443,0.000022281189,0.00003054541,0.000025217625],"domain_scores_gemma":[0.9996592,0.00009964095,0.00007816799,0.0000347834,0.00003206234,0.00009622138],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0001650102,0.00027657684,0.00026500103,0.00025847275,0.00030987724,0.00026018496,0.00026912047,0.00066430896,0.0025387576],"category_scores_gemma":[0.00035471402,0.00019350777,0.00019774158,0.0001878089,0.00043800133,0.00017651223,0.0003728987,0.0009959177,0.0003796724],"study_design_candidate":"bench_or_experimental","study_design_consensus":"bench_or_experimental","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00018915955,0.000022035045,0.0015004729,0.000010832607,0.000015787917,0.0004344792,0.00005068715,0.0000946838,0.9963819,0.00020886859,0.00004382844,0.0010472428],"study_design_scores_gemma":[0.00015431235,0.00092234445,0.17704004,0.000020427131,0.00023086448,0.008146002,0.00049011374,0.0071113203,0.7979644,0.00079750887,0.00706258,0.000060036105],"about_ca_topic_score_codex":0.0012530795,"about_ca_topic_score_gemma":0.0017034537,"teacher_disagreement_score":0.0025387576,"about_ca_system_score_codex":0.00021503838,"about_ca_system_score_gemma":0.00014337944,"threshold_uncertainty_score":0.008493006},"labels":[],"label_agreement":null},{"id":"W2030287014","doi":"10.1038/87310","title":"Ewing tumor cells activate distinct signaling pathways in monolayer versus anchorage-independent cultures","year":2001,"lang":"en","type":"article","venue":"Nature Genetics","topic":"HER2/EGFR in Cancer Research","field":"Medicine","cited_by":0,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"BC Children's Hospital; Institute of Indigenous Peoples' Health; Children's & Women's Health Centre of British Columbia","funders":"","keywords":"Biology; Signal transduction; Cell biology; Monolayer; Cancer research; Tumor cells; Cell culture; Genetics; Biochemistry","score_opus":0.04396581008631634,"score_gpt":0.35316148163552935,"score_spread":0.309195671549213,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2030287014","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.97909945,0.0037782935,0.008125266,0.00018673085,0.00011137222,0.00009902911,0.0019655123,0.00022223528,0.006411969],"genre_scores_gemma":[0.97580296,0.0036731132,0.0060735894,0.00013932984,0.000044961707,0.00016353189,0.00346854,0.00009912431,0.010534822],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99960846,0.000056719087,0.00004374501,0.00005777735,0.000105329564,0.00012802596],"domain_scores_gemma":[0.99973065,0.00009498208,0.000028511397,0.0000613489,0.00003630638,0.00004818684],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00028292686,0.00046696715,0.0005131349,0.0006635256,0.00030110253,0.0007921321,0.00032573412,0.00029011714,0.0018931996],"category_scores_gemma":[0.00020567003,0.00031097705,0.00056610524,0.0005880046,0.00016510228,0.0007270101,0.00038808887,0.0011118429,0.0010228135],"study_design_candidate":"bench_or_experimental","study_design_consensus":"bench_or_experimental","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0001685248,0.0000681543,0.00014179618,0.000029836005,0.000007896101,0.000027984688,0.000033633038,0.00004584377,0.9976295,0.000170745,0.00014390831,0.001532219],"study_design_scores_gemma":[0.00002569632,0.000162149,0.0059676124,0.0000068657973,0.000023219738,0.00010804831,0.00007419511,0.00086425507,0.9906481,0.000098099066,0.0020152393,0.0000064548653],"about_ca_topic_score_codex":0.0009851247,"about_ca_topic_score_gemma":0.0020453006,"teacher_disagreement_score":0.0018931996,"about_ca_system_score_codex":0.00041446523,"about_ca_system_score_gemma":0.00022229721,"threshold_uncertainty_score":0.006333351},"labels":[],"label_agreement":null},{"id":"W2030409202","doi":"10.1038/ng1319","title":"Mutations in the gene encoding filamin B disrupt vertebral segmentation, joint formation and skeletogenesis","year":2004,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Connective tissue disorders research","field":"Biochemistry, Genetics and Molecular Biology","cited_by":289,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Northern Ontario Academic Medicine Association","funders":"Cedars-Sinai Medical Center; National Organization for Rare Disorders","keywords":"Filamin; Biology; Missense mutation; Genetics; FLNA; Endochondral ossification; Actin cytoskeleton; Cytoskeleton; Phenotype; Cell biology; Gene; Mutation; Anatomy; Cell","score_opus":0.014326686695378631,"score_gpt":0.29798897854763473,"score_spread":0.2836622918522561,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2030409202","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9782014,0.0014013388,0.012441594,0.0003334236,0.00017738293,0.000061523635,0.0014396423,0.0006599298,0.005283891],"genre_scores_gemma":[0.990576,0.000657735,0.0034014194,0.00008009344,0.000022054748,0.000024401788,0.0005516227,0.0001620273,0.0045245965],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9996929,0.000043489967,0.000037640515,0.000058038266,0.00012470719,0.000043321117],"domain_scores_gemma":[0.99937063,0.00016273321,0.00022675337,0.00003771453,0.000028992976,0.0001733099],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00013682457,0.0013615931,0.0004222037,0.0013235455,0.0006819996,0.0006568537,0.0006214787,0.0013491876,0.0036109935],"category_scores_gemma":[0.00041409303,0.00050703716,0.00042560333,0.0004626646,0.0013168927,0.0002558159,0.0010533204,0.0010988043,0.0012078587],"study_design_candidate":"bench_or_experimental","study_design_consensus":"bench_or_experimental","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0002779879,0.000038881386,0.0006057681,0.00003385336,0.000045658104,0.0011386606,0.00003677742,0.00039884404,0.9938147,0.0006484286,0.00024035077,0.0027202927],"study_design_scores_gemma":[0.00020003619,0.00022538254,0.018723669,0.000047024918,0.00020312778,0.0072226212,0.00019128952,0.00457172,0.95940363,0.0007433958,0.00840923,0.000058896683],"about_ca_topic_score_codex":0.0061970004,"about_ca_topic_score_gemma":0.007819835,"teacher_disagreement_score":0.0061970004,"about_ca_system_score_codex":0.0008513745,"about_ca_system_score_gemma":0.00047799235,"threshold_uncertainty_score":0.012321889},"labels":[],"label_agreement":null},{"id":"W2030701454","doi":"10.1038/ng.2303","title":"Exome sequencing and the genetic basis of complex traits","year":2012,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Genetic Associations and Epidemiology","field":"Biochemistry, Genetics and Molecular Biology","cited_by":391,"is_retracted":false,"has_abstract":false,"route_ca_aff":false,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"","funders":"National Center for Advancing Translational Sciences; National Institute of Allergy and Infectious Diseases; National Human Genome Research Institute; National Center for Research Resources; National Institute of Mental Health; National Heart, Lung, and Blood Institute; Canadian Institutes of Health Research; U.S. Public Health Service; National Institutes of Health","keywords":"Biology; Exome sequencing; Exome; Computational biology; Evolutionary biology; Genetics; Phenotype; Gene","score_opus":0.019129706859974387,"score_gpt":0.2727780175503344,"score_spread":0.25364831069036,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2030701454","genre_codex":"empirical","genre_gemma":"review","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"review","genre_consensus":null,"domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9740155,0.0067819455,0.010634299,0.0026654114,0.000109062894,0.00002159214,0.0030071663,0.00006517849,0.0026998476],"genre_scores_gemma":[0.99220407,0.0024550515,0.0031304683,0.000448384,0.00015630249,0.000016134198,0.00078908243,0.000026079371,0.00077450613],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99918836,0.00027733925,0.000088555425,0.00020382699,0.00016858414,0.00007346503],"domain_scores_gemma":[0.9978169,0.0012329873,0.00055056,0.00018973049,0.000104842504,0.00010492492],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0011481111,0.00051741325,0.00039995895,0.0017656955,0.00029367508,0.00080592965,0.00045862232,0.0011038502,0.0023608732],"category_scores_gemma":[0.00416538,0.00025741573,0.00035858378,0.0016832413,0.0004921845,0.00083686743,0.00082432816,0.0008259384,0.00018290908],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0021830625,0.00014468344,0.77909654,0.0003590692,0.0020134114,0.00562294,0.0005086644,0.0047866697,0.116138086,0.013674318,0.0029562707,0.07251633],"study_design_scores_gemma":[0.00006399636,0.000109174835,0.9428503,0.00012244318,0.0004541401,0.00767577,0.00025022327,0.0062452927,0.010013365,0.02511114,0.0070505114,0.000053644777],"about_ca_topic_score_codex":0.0010973137,"about_ca_topic_score_gemma":0.0013472434,"teacher_disagreement_score":0.0023608732,"about_ca_system_score_codex":0.00024191228,"about_ca_system_score_gemma":0.0002111416,"threshold_uncertainty_score":0.007897913},"labels":[],"label_agreement":null},{"id":"W2030714059","doi":"10.1038/ng.392","title":"Lin28 promotes transformation and is associated with advanced human malignancies","year":2009,"lang":"en","type":"article","venue":"Nature Genetics","topic":"MicroRNA in disease regulation","field":"Biochemistry, Genetics and Molecular Biology","cited_by":820,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of British Columbia","funders":"National Institute of General Medical Sciences; National Institute of Diabetes and Digestive and Kidney Diseases; National Heart, Lung, and Blood Institute; National Institutes of Health; Eunice Kennedy Shriver National Institute of Child Health and Human Development; Howard Hughes Medical Institute","keywords":"LIN28; Derepression; Psychological repression; microRNA; Biology; Cancer research; Carcinogenesis; Proteostasis; Malignant transformation; HMGA2; Cancer; KLF2; Oncomir; Cell biology; Genetics; Downregulation and upregulation; Gene; Gene expression; Transcription factor; SOX2","score_opus":0.0044550624453506445,"score_gpt":0.2397715543522619,"score_spread":0.23531649190691126,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2030714059","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9912374,0.0019541024,0.0029083267,0.00028263612,0.000039602306,0.000020296267,0.0004607365,0.0003618182,0.0027350138],"genre_scores_gemma":[0.9962453,0.0004517952,0.00062170415,0.000055603276,0.000022869037,0.000019710676,0.00041738545,0.000059868926,0.0021057057],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9997428,0.00005868928,0.000014382371,0.00005822722,0.00008220506,0.000043654367],"domain_scores_gemma":[0.9993548,0.00012824872,0.0002405645,0.00008035494,0.0000315835,0.00016457506],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00021069373,0.00034112704,0.00038872403,0.0009873676,0.0003075568,0.00043827324,0.00030427313,0.000524899,0.0047524744],"category_scores_gemma":[0.0004413276,0.00033368223,0.00027560236,0.00045165516,0.00038397752,0.00017155813,0.00061367336,0.0009072519,0.0010358233],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0013639948,0.000112070375,0.017634174,0.000076196266,0.00007978829,0.0021168445,0.000047728354,0.00025004434,0.9698756,0.0008292102,0.0008760648,0.006738401],"study_design_scores_gemma":[0.00030399626,0.00097156555,0.37058863,0.000029127794,0.0002625119,0.028046424,0.00021490938,0.0046264925,0.571013,0.002693964,0.021198949,0.000050420596],"about_ca_topic_score_codex":0.00024020663,"about_ca_topic_score_gemma":0.00033985262,"teacher_disagreement_score":0.0047524744,"about_ca_system_score_codex":0.00022734402,"about_ca_system_score_gemma":0.00019165869,"threshold_uncertainty_score":0.015898645},"labels":[],"label_agreement":null},{"id":"W2031964961","doi":"10.1038/ng1771","title":"BBS10 encodes a vertebrate-specific chaperonin-like protein and is a major BBS locus","year":2006,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Genetic and Kidney Cyst Diseases","field":"Biochemistry, Genetics and Molecular Biology","cited_by":286,"is_retracted":false,"has_abstract":false,"route_ca_aff":false,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"","funders":"Institute of Genetics; Wellcome Trust","keywords":"Biology; Bardet–Biedl syndrome; Genetics; Zebrafish; Locus (genetics); Phenotype; Ciliopathy; Gene; Vertebrate","score_opus":0.003620034075160504,"score_gpt":0.20879138980909165,"score_spread":0.20517135573393114,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2031964961","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9571136,0.001467448,0.020273283,0.001094977,0.0010916791,0.00008637453,0.008967917,0.0012042727,0.0087005],"genre_scores_gemma":[0.9510804,0.0006881604,0.010606449,0.00033016913,0.000057751982,0.00006445514,0.015094621,0.00018490895,0.021893071],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9998129,0.00001978641,0.000012410486,0.000053203054,0.000059840742,0.000041854088],"domain_scores_gemma":[0.9994723,0.0000627016,0.00011531841,0.000025513495,0.00006526112,0.0002588088],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0001597356,0.0007020463,0.0002929092,0.0007299943,0.00041320283,0.00034518327,0.0004280513,0.000660007,0.003378373],"category_scores_gemma":[0.0002533464,0.00025806497,0.00038707757,0.00029776138,0.0006780231,0.00019666135,0.00044023053,0.00074145675,0.0023927358],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0002666107,0.00003900521,0.0019209825,0.000061433835,0.000010700247,0.00089673453,0.00003223374,0.00009576325,0.9908602,0.0006375759,0.0011678843,0.004010821],"study_design_scores_gemma":[0.00010103579,0.00029398914,0.07787123,0.00008137436,0.00004695608,0.0065921005,0.00023525218,0.0029023145,0.86392075,0.0011392898,0.0467435,0.000072255854],"about_ca_topic_score_codex":0.0035232813,"about_ca_topic_score_gemma":0.0035505095,"teacher_disagreement_score":0.0035232813,"about_ca_system_score_codex":0.0008902913,"about_ca_system_score_gemma":0.0006562093,"threshold_uncertainty_score":0.011301756},"labels":[],"label_agreement":null},{"id":"W2032431957","doi":"10.1038/ng.2765","title":"Mutations in genes encoding the cadherin receptor-ligand pair DCHS1 and FAT4 disrupt cerebral cortical development","year":2013,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Hippo pathway signaling and YAP/TAZ","field":"Biochemistry, Genetics and Molecular Biology","cited_by":287,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Hospital for Sick Children; Lunenfeld-Tanenbaum Research Institute; University of Toronto; Centre Hospitalier Universitaire Sainte-Justine; Mount Sinai Hospital","funders":"Medical Research Council; Wellcome Trust","keywords":"Biology; Neurogenesis; Neocortex; Progenitor cell; Neural stem cell; Cell biology; Neuroepithelial cell; Neuroscience; Embryonic stem cell; Gene knockdown; Progenitor; Cerebral cortex; Stem cell; Genetics; Gene","score_opus":0.009977403826609079,"score_gpt":0.24687402977366557,"score_spread":0.2368966259470565,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2032431957","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.97562146,0.00085189677,0.013158189,0.0005458398,0.00021960356,0.000081420956,0.001866309,0.0009579986,0.0066973073],"genre_scores_gemma":[0.98640406,0.0005843154,0.0043433015,0.000105939995,0.000018835275,0.000054942077,0.0005854682,0.00031050906,0.0075926944],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99965227,0.000038818704,0.000034334607,0.000069233705,0.00014795458,0.000057403766],"domain_scores_gemma":[0.99937963,0.0001799554,0.00022449739,0.000043809974,0.000025360683,0.00014671263],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00016845924,0.001429467,0.00038245667,0.002032393,0.0005544548,0.00057752617,0.0008633943,0.00088034535,0.00538785],"category_scores_gemma":[0.00038224945,0.00047990913,0.0004575274,0.00054543937,0.0016167322,0.00031292296,0.001059095,0.0012632916,0.0009462712],"study_design_candidate":"bench_or_experimental","study_design_consensus":"bench_or_experimental","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00015808984,0.00003256152,0.00048028977,0.000036071822,0.000038956285,0.0009929005,0.000035980738,0.0005727899,0.99356925,0.0013469309,0.00026099384,0.0024751804],"study_design_scores_gemma":[0.00007045757,0.000060920614,0.007917672,0.00001810049,0.00008435048,0.0023579884,0.00013300018,0.0029665034,0.98123026,0.0005641858,0.00456537,0.00003130101],"about_ca_topic_score_codex":0.00457763,"about_ca_topic_score_gemma":0.00997155,"teacher_disagreement_score":0.00538785,"about_ca_system_score_codex":0.0011573766,"about_ca_system_score_gemma":0.0008024887,"threshold_uncertainty_score":0.018024147},"labels":[],"label_agreement":null},{"id":"W2032485563","doi":"10.1038/ng.1075","title":"ABCG2 null alleles define the Jr(a−) blood group phenotype","year":2012,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Drug Transport and Resistance Mechanisms","field":"Medicine","cited_by":91,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Manitoba","funders":"","keywords":"Biology; Allele; Null allele; Genetics; Phenotype; Gene","score_opus":0.008223133879484342,"score_gpt":0.2396598569197008,"score_spread":0.23143672304021645,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2032485563","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.98280704,0.00033876696,0.006716977,0.00036043025,0.0001445724,0.00005868216,0.0012737924,0.0003620884,0.007937644],"genre_scores_gemma":[0.9856023,0.00025730924,0.0064446805,0.00031421133,0.00010713271,0.00005200469,0.0009723277,0.00048667906,0.005763423],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9993412,0.00015921994,0.00009545641,0.00013551238,0.0001770507,0.00009157377],"domain_scores_gemma":[0.99897265,0.00014770502,0.0004144193,0.00010428505,0.00007130271,0.00028956248],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00038407545,0.0009848821,0.0003903176,0.0012002336,0.0003709366,0.0005778719,0.0007584868,0.0010757461,0.00978292],"category_scores_gemma":[0.00075682363,0.00025742015,0.00052705326,0.00047038475,0.00079993834,0.00028938233,0.00078896666,0.0012284309,0.0024091683],"study_design_candidate":"bench_or_experimental","study_design_consensus":"bench_or_experimental","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0003660105,0.00010937705,0.0019466851,0.000026164787,0.00002885938,0.0015466728,0.00007223916,0.00004097804,0.9913686,0.0009937447,0.0005849997,0.0029157992],"study_design_scores_gemma":[0.0008706263,0.0017926514,0.13805084,0.00010393589,0.0004347811,0.06673412,0.00074197963,0.0026506344,0.7498041,0.004343681,0.03430431,0.00016832034],"about_ca_topic_score_codex":0.00081278273,"about_ca_topic_score_gemma":0.0005708824,"teacher_disagreement_score":0.00978292,"about_ca_system_score_codex":0.0001697976,"about_ca_system_score_gemma":0.00018086884,"threshold_uncertainty_score":0.032727122},"labels":[],"label_agreement":null},{"id":"W2033021653","doi":"10.1038/ng.3039","title":"Most genetic risk for autism resides with common variation","year":2014,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Autism Spectrum Disorder Research","field":"Neuroscience","cited_by":1286,"is_retracted":false,"has_abstract":false,"route_ca_aff":false,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"","funders":"Eunice Kennedy Shriver National Institute of Child Health and Human Development; National Institute of Neurological Disorders and Stroke; National Institute of Mental Health; Canadian Institutes of Health Research","keywords":"Genetic architecture; Heritability; Biology; Autism; Variation (astronomy); Genetic variation; Missing heritability problem; Genetics; Heritability of autism; Trait; Allele; Autism spectrum disorder; Evolutionary biology; Quantitative trait locus; Gene; Phenotype; Genotype; Genetic variants; Developmental psychology; Psychology","score_opus":0.012378567901468546,"score_gpt":0.2839425668497126,"score_spread":0.271563998948244,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2033021653","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9708642,0.0028727164,0.011790268,0.0018336582,0.00027215263,0.000073359275,0.0029196865,0.00035753116,0.009016515],"genre_scores_gemma":[0.99230474,0.0010013981,0.0037117621,0.00033068744,0.00019695243,0.00003965743,0.0010528455,0.00009538423,0.0012665332],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99812835,0.00035247175,0.00017996626,0.0007638466,0.0003651593,0.00021031158],"domain_scores_gemma":[0.99808794,0.0007495538,0.0005678281,0.00024129103,0.00013731419,0.00021609064],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0005673454,0.0016541407,0.0011018625,0.0038103866,0.0012483852,0.0008075793,0.0010628727,0.0020357962,0.014570511],"category_scores_gemma":[0.002979695,0.00042226026,0.0017414737,0.002594221,0.0014131274,0.000978303,0.0015071786,0.0010612528,0.0009949617],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0020218175,0.0003804114,0.5965594,0.0005882665,0.004605507,0.030494189,0.0019673882,0.0015059336,0.24449305,0.015851064,0.004590285,0.09694266],"study_design_scores_gemma":[0.00019938135,0.0005252007,0.86434746,0.00042959262,0.0027185357,0.07306429,0.0010753145,0.0016839375,0.021734342,0.021705871,0.012339492,0.00017673071],"about_ca_topic_score_codex":0.0028883256,"about_ca_topic_score_gemma":0.0029215657,"teacher_disagreement_score":0.014570511,"about_ca_system_score_codex":0.00035534461,"about_ca_system_score_gemma":0.00044410085,"threshold_uncertainty_score":0.04874319},"labels":[],"label_agreement":null},{"id":"W2033159826","doi":"10.1038/ng.3068","title":"Mouse tetrad analysis provides insights into recombination mechanisms and hotspot evolutionary dynamics","year":2014,"lang":"en","type":"article","venue":"Nature Genetics","topic":"DNA Repair Mechanisms","field":"Biochemistry, Genetics and Molecular Biology","cited_by":126,"is_retracted":false,"has_abstract":false,"route_ca_aff":false,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"","funders":"Institute of Genetics; National Institute of General Medical Sciences; Eunice Kennedy Shriver National Institute of Child Health and Human Development; National Cancer Institute; Agence Nationale de la Recherche","keywords":"Biology; Gene conversion; Chromatid; Genetics; Homologous recombination; Meiosis; Ectopic recombination; Tetrad; Recombination; Mitotic crossover; Gene; DNA; Cell biology; Genetic recombination; Chromosome","score_opus":0.002913677415747028,"score_gpt":0.21513749507606092,"score_spread":0.2122238176603139,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2033159826","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.71771514,0.0027744314,0.26490933,0.00035712417,0.00018620444,0.000049088445,0.0047901403,0.0024256946,0.006792805],"genre_scores_gemma":[0.9035476,0.0015889639,0.08274087,0.00024404343,0.00005060786,0.00008548473,0.00300607,0.0012735894,0.0074626287],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.99961036,0.000043294618,0.000042967367,0.00018118702,0.0000772763,0.000044992194],"domain_scores_gemma":[0.9992786,0.0001749445,0.00022488397,0.00017094814,0.000054283108,0.00009633429],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00058299804,0.00054799614,0.00048062514,0.003217012,0.000523062,0.0008058513,0.00094591954,0.0007569892,0.0055064275],"category_scores_gemma":[0.00049284287,0.0006091409,0.0008114807,0.0011985474,0.0004792899,0.0007305713,0.0006715232,0.0015250122,0.0014531811],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00012901548,0.00001643569,0.0023934152,0.00005120066,0.00003212751,0.00012330167,0.000032013002,0.0004918431,0.9873461,0.0027990052,0.00019178809,0.0063937595],"study_design_scores_gemma":[0.00005420901,0.00013790852,0.039362296,0.000039138526,0.00022272224,0.0028818252,0.00008291736,0.019450195,0.91594577,0.0041142344,0.017644726,0.00006405634],"about_ca_topic_score_codex":0.00058881554,"about_ca_topic_score_gemma":0.0012516505,"teacher_disagreement_score":0.0055064275,"about_ca_system_score_codex":0.00053691445,"about_ca_system_score_gemma":0.00018350685,"threshold_uncertainty_score":0.018420815},"labels":[],"label_agreement":null},{"id":"W2033328554","doi":"10.1038/87028","title":"Genomic amplification in retinoblastoma narrowed to 1.2 Mb on chromosome 6p containing a novel kinesin-like gene, RBKIN","year":2001,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Ocular Oncology and Treatments","field":"Medicine","cited_by":0,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Princess Margaret Cancer Centre; University Health Network; University of Toronto; Ontario Institute for Cancer Research","funders":"","keywords":"Biology; Genetics; Kinesin; Gene; Chromosome; Gene duplication; Molecular biology; Microtubule","score_opus":0.017064178695502624,"score_gpt":0.29701774149295396,"score_spread":0.2799535627974513,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2033328554","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99394953,0.00082030316,0.001626123,0.0003166335,0.000035843415,0.000027348626,0.00046185328,0.0001245501,0.0026377253],"genre_scores_gemma":[0.9969426,0.00022179981,0.00073087186,0.000062522566,0.000015006602,0.000008976897,0.00028387437,0.000017321105,0.0017170274],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9998198,0.000013715796,0.000014915016,0.000056676676,0.000052091942,0.000042860618],"domain_scores_gemma":[0.999772,0.00007785577,0.00007180164,0.000014617398,0.000015313497,0.000048527712],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00010082402,0.00044217292,0.000381013,0.0008065842,0.00036112964,0.00034192146,0.00040483486,0.000569787,0.0027904275],"category_scores_gemma":[0.00037608697,0.00030153777,0.00041656496,0.00027357347,0.00047065032,0.00012756465,0.0004478522,0.0005578365,0.0005997796],"study_design_candidate":"bench_or_experimental","study_design_consensus":"bench_or_experimental","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0010844421,0.000086677384,0.007997202,0.00014103262,0.00006539402,0.04382154,0.00029212388,0.00087961537,0.9346659,0.00077079126,0.00046709293,0.009728152],"study_design_scores_gemma":[0.0004348509,0.00077590445,0.32872406,0.00012881497,0.00061821926,0.21828124,0.0006266656,0.0052085333,0.42944863,0.0016486539,0.014023996,0.000080478916],"about_ca_topic_score_codex":0.003579937,"about_ca_topic_score_gemma":0.003961305,"teacher_disagreement_score":0.003579937,"about_ca_system_score_codex":0.00043647876,"about_ca_system_score_gemma":0.0002312069,"threshold_uncertainty_score":0.009334862},"labels":[],"label_agreement":null},{"id":"W2033332310","doi":"10.1038/ng928","title":"Disruption of dog-1 in Caenorhabditis elegans triggers deletions upstream of guanine-rich DNA","year":2002,"lang":"en","type":"article","venue":"Nature Genetics","topic":"DNA Repair Mechanisms","field":"Biochemistry, Genetics and Molecular Biology","cited_by":269,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of British Columbia; BC Cancer Agency","funders":"","keywords":"Biology; Caenorhabditis elegans; Genetics; Gene; DNA replication; DNA; Genome instability; Mutation; Somatic cell; Guanine; Phenotype; DNA damage; Molecular biology; Nucleotide","score_opus":0.0066047301657026864,"score_gpt":0.2436054455454713,"score_spread":0.23700071537976863,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2033332310","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.98380244,0.0007247924,0.0111149885,0.00031288856,0.0001944213,0.00010385376,0.0010378271,0.00062061066,0.0020881288],"genre_scores_gemma":[0.9888671,0.0002980506,0.0057350392,0.00011456538,0.000017191553,0.00005592146,0.000703317,0.00017675864,0.0040320456],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99971884,0.000025088846,0.000033190063,0.000087430664,0.000085813794,0.000049731945],"domain_scores_gemma":[0.9993055,0.00014726525,0.00028048377,0.00008892915,0.000029887096,0.00014784883],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00021819731,0.0006820133,0.0003646419,0.0005727125,0.00038934918,0.00042797544,0.00079232274,0.0009314447,0.001517494],"category_scores_gemma":[0.00031229111,0.0006598083,0.00038619226,0.00018457061,0.00081703195,0.00033761375,0.0007136681,0.001643285,0.00092846394],"study_design_candidate":"bench_or_experimental","study_design_consensus":"bench_or_experimental","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00009643245,0.000021651302,0.00010758002,0.000026363768,0.00000380639,0.00014894131,0.000010456284,0.00011151721,0.9987507,0.00021204248,0.000053029784,0.0004574362],"study_design_scores_gemma":[0.000024568148,0.000060224666,0.002435012,0.0000105156905,0.000013479243,0.00026991597,0.000026253387,0.0011342157,0.99403524,0.00011060586,0.0018684723,0.000011476993],"about_ca_topic_score_codex":0.0010257902,"about_ca_topic_score_gemma":0.0032748093,"teacher_disagreement_score":0.001517494,"about_ca_system_score_codex":0.00082017825,"about_ca_system_score_gemma":0.0004551818,"threshold_uncertainty_score":0.0059508085},"labels":[],"label_agreement":null},{"id":"W2033852655","doi":"10.1038/75621","title":"Rom-1 is required for rod photoreceptor viability and the regulation of disk morphogenesis","year":2000,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Retinal Development and Disorders","field":"Biochemistry, Genetics and Molecular Biology","cited_by":173,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Toronto; Mount Sinai Hospital; Lunenfeld-Tanenbaum Research Institute; University of British Columbia; Hospital for Sick Children","funders":"National Eye Institute","keywords":"Peripherin; Biology; Morphogenesis; Cell biology; Phenotype; Retinal degeneration; Retina; Genetics; Gene","score_opus":0.00471700580747497,"score_gpt":0.2302916803687384,"score_spread":0.22557467456126343,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2033852655","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.98669726,0.0024361357,0.005146017,0.00048620015,0.000114610906,0.00002154383,0.0006364786,0.0002952244,0.004166521],"genre_scores_gemma":[0.9939612,0.00035512412,0.0016612919,0.000071310016,0.000023682564,0.0000110824885,0.00069553475,0.00007575045,0.003144895],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99983025,0.000023237557,0.000013950388,0.000042746768,0.000049072874,0.00004074524],"domain_scores_gemma":[0.9996118,0.00007452722,0.00015193506,0.000041637755,0.000023787868,0.00009633829],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00015772942,0.0004254234,0.0003427297,0.00034070484,0.00045463088,0.00071777904,0.00064243993,0.00074930646,0.0018711899],"category_scores_gemma":[0.00047087757,0.0003106718,0.0002728821,0.00012957411,0.0005769754,0.0003563642,0.00045090602,0.0009366411,0.0013796135],"study_design_candidate":"bench_or_experimental","study_design_consensus":"bench_or_experimental","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00017634133,0.000018571924,0.0003972627,0.000030183986,0.0000042230217,0.00044503767,0.00001350447,0.00010104928,0.99715865,0.00043149447,0.00012317373,0.0011004483],"study_design_scores_gemma":[0.000060237908,0.000082814724,0.018808592,0.0000145370495,0.000017229424,0.0031390283,0.00006941617,0.0026351567,0.96818304,0.0007834339,0.0061860224,0.00002051852],"about_ca_topic_score_codex":0.0005466135,"about_ca_topic_score_gemma":0.0009283525,"teacher_disagreement_score":0.0018711899,"about_ca_system_score_codex":0.000483024,"about_ca_system_score_gemma":0.0002477357,"threshold_uncertainty_score":0.006259799},"labels":[],"label_agreement":null},{"id":"W2036275580","doi":"10.1038/ng.2221","title":"Multiple apical plasma membrane constituents are associated with susceptibility to meconium ileus in individuals with cystic fibrosis","year":2012,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Cystic Fibrosis Research Advances","field":"Medicine","cited_by":210,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Institute for Clinical Evaluative Sciences; SickKids Foundation; Hospital for Sick Children; Public Health Ontario; University of Toronto","funders":"National Human Genome Research Institute; National Institute of Diabetes and Digestive and Kidney Diseases; National Heart, Lung, and Blood Institute; Canadian Institutes of Health Research; Case Western Reserve University","keywords":"Meconium Ileus; Cystic fibrosis; Biology; Meconium; Ileus; Fibrosis; Internal medicine; Gastroenterology; Genetics; Medicine; Pregnancy; Fetus","score_opus":0.013569139103447892,"score_gpt":0.288668213026009,"score_spread":0.2750990739225611,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2036275580","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99894375,0.00032442037,0.00017487853,0.00012204147,0.000018029896,0.000003919894,0.00006908014,0.000008302262,0.0003356139],"genre_scores_gemma":[0.9993648,0.00009073737,0.00023678376,0.000044355922,0.00002258313,0.0000038748312,0.000057155565,0.0000061883793,0.00017355484],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9994752,0.00014948481,0.00007881685,0.00012341375,0.00009926678,0.00007378963],"domain_scores_gemma":[0.9980367,0.00055987894,0.00089018856,0.00010476603,0.00016201123,0.00024649163],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0003512785,0.0010232549,0.00074233767,0.0017738721,0.00096914597,0.000701416,0.0005445614,0.001827721,0.003252323],"category_scores_gemma":[0.002239407,0.00043706456,0.0009782056,0.0014371626,0.00056231825,0.00062198,0.0006966242,0.0009933757,0.00029471144],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0013660538,0.00015942239,0.9477833,0.0000837165,0.00048676776,0.006423201,0.000513636,0.00018429253,0.03823404,0.00016567175,0.00025854612,0.004341482],"study_design_scores_gemma":[0.000025763396,0.00019677193,0.99003756,0.00002579617,0.0002898327,0.006539281,0.0003569618,0.00044265663,0.0016212194,0.00022609529,0.00021705542,0.00002093359],"about_ca_topic_score_codex":0.0017820148,"about_ca_topic_score_gemma":0.0017765175,"teacher_disagreement_score":0.003252323,"about_ca_system_score_codex":0.00022553114,"about_ca_system_score_gemma":0.00017067576,"threshold_uncertainty_score":0.010880113},"labels":[],"label_agreement":null},{"id":"W2036542394","doi":"10.1038/ng.817","title":"Bias due to selection of rare variants using frequency in controls","year":2011,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Genomics and Rare Diseases","field":"Biochemistry, Genetics and Molecular Biology","cited_by":2,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Western University","funders":"","keywords":"Biology; Selection (genetic algorithm); Selection bias; Frequency-dependent selection; Allele frequency; Computational biology; Genetics; Evolutionary biology; Statistics; Genotype; Gene; Machine learning; Computer science","score_opus":0.018550045307678013,"score_gpt":0.25525561480491127,"score_spread":0.23670556949723326,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2036542394","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":"methods","model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":"methods","domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.8031801,0.00403181,0.1767932,0.0014836374,0.001271704,0.0004043799,0.0015333784,0.0009707473,0.010331075],"genre_scores_gemma":[0.9861238,0.00019788857,0.0102560045,0.0007857944,0.00026748056,0.00013839915,0.00041878427,0.00030127013,0.0015105996],"study_design_codex":"observational","study_design_gemma":"simulation_or_modeling","domain_scores_codex":[0.8903154,0.061588533,0.008099667,0.025002977,0.010454877,0.004538419],"domain_scores_gemma":[0.81897557,0.121426225,0.011175657,0.042216085,0.00418482,0.0020217046],"candidate_categories":["metaresearch"],"consensus_categories":[],"category_scores_codex":[0.062773354,0.0013680623,0.0026037314,0.0048778863,0.0016451112,0.0031447068,0.0026234514,0.0028744559,0.0049738237],"category_scores_gemma":[0.12602398,0.0010611007,0.0024247516,0.0033720166,0.0031540063,0.0017865144,0.0023154842,0.0018941719,0.0007152703],"study_design_candidate":"simulation_or_modeling","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0038054814,0.00020318586,0.8963704,0.00041361715,0.006729381,0.0026008422,0.0016632812,0.003413006,0.017647436,0.012010303,0.0023903514,0.052752666],"study_design_scores_gemma":[0.0011810107,0.0016964625,0.8309735,0.0004100837,0.010592238,0.012628041,0.00069415825,0.058761526,0.02040896,0.05106473,0.011294298,0.00029500175],"about_ca_topic_score_codex":0.003632687,"about_ca_topic_score_gemma":0.0032838336,"teacher_disagreement_score":0.93722665,"about_ca_system_score_codex":0.0006554427,"about_ca_system_score_gemma":0.0008029186,"threshold_uncertainty_score":0.33198124},"labels":[],"label_agreement":null},{"id":"W2036743693","doi":"10.1038/ng1881","title":"How genetic analysis tests theories of animal aging","year":2006,"lang":"en","type":"review","venue":"Nature Genetics","topic":"Genetics, Aging, and Longevity in Model Organisms","field":"Biochemistry, Genetics and Molecular Biology","cited_by":61,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"McGill University","funders":"","keywords":"Biology; Vertebrate; Evolutionary biology; Mutant; Life span; Genetics; Computational biology; Gene","score_opus":0.011039467047709611,"score_gpt":0.287776331179267,"score_spread":0.2767368641315574,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2036743693","genre_codex":"review","genre_gemma":"review","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"review","genre_consensus":"review","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.00049222144,0.97281116,0.008763561,0.011144726,0.0019140553,0.000011210101,0.00003001953,0.00007998875,0.004753045],"genre_scores_gemma":[0.0048380494,0.980828,0.0050664525,0.0058099437,0.0016645403,0.000028214401,0.0000446047,0.000021606793,0.0016986408],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.99922025,0.00028520534,0.000056985442,0.00014507235,0.00025672143,0.000035835234],"domain_scores_gemma":[0.99663347,0.0025195917,0.00009840316,0.000204585,0.0004143789,0.00012958051],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.003628154,0.0011772224,0.0021731528,0.0019446644,0.0005264482,0.0022501112,0.0029102352,0.003765541,0.0018694894],"category_scores_gemma":[0.004500563,0.0004230622,0.0005915135,0.0017073432,0.0054817256,0.004429091,0.0010448875,0.0047308537,0.0016890086],"study_design_candidate":"not_applicable","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00011950631,0.000115888484,0.0008652188,0.0058055394,0.00029569634,0.00058360485,0.00024320881,0.001987855,0.003657784,0.15132214,0.07831211,0.75669146],"study_design_scores_gemma":[0.00008275165,0.00008625778,0.0010658684,0.002148535,0.00016554189,0.0018153681,0.00031824503,0.000598315,0.001360308,0.30601534,0.6862579,0.00008553209],"about_ca_topic_score_codex":0.002163985,"about_ca_topic_score_gemma":0.002861081,"teacher_disagreement_score":0.003765541,"about_ca_system_score_codex":0.0014516582,"about_ca_system_score_gemma":0.0017129635,"threshold_uncertainty_score":0.019187689},"labels":[],"label_agreement":null},{"id":"W2036835673","doi":"10.1038/ng1740","title":"Mutations in NALP7 cause recurrent hydatidiform moles and reproductive wastage in humans","year":2006,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Gestational Trophoblastic Disease Studies","field":"Medicine","cited_by":482,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Hôpital Notre-Dame; McGill University Health Centre","funders":"","keywords":"Biology; Pregnancy; Gene; Mutation; Embryo; Genetics","score_opus":0.011694535462953891,"score_gpt":0.29308601539080287,"score_spread":0.28139147992784896,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2036835673","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99754035,0.00046805743,0.00050554756,0.00009328348,0.000020983109,0.00001049258,0.0003510481,0.000025346573,0.0009849792],"genre_scores_gemma":[0.9985617,0.00027139884,0.00038540128,0.00003835461,0.000018434363,0.0000073146493,0.00019637645,0.000014480341,0.00050661486],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9997125,0.000060749873,0.000034879795,0.00008373454,0.00006942738,0.00003862377],"domain_scores_gemma":[0.99939144,0.00025149385,0.00017417198,0.000064717206,0.00003447538,0.00008368084],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00019017237,0.0005550214,0.0004439525,0.0012427832,0.00046062304,0.0005046764,0.00047486922,0.0009384821,0.0024969082],"category_scores_gemma":[0.0012644412,0.00030573754,0.00045302353,0.0005928003,0.0008376174,0.00026773184,0.0005448685,0.00041810877,0.0003059139],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0041148793,0.00032122704,0.38935724,0.0003257294,0.0010113164,0.2647064,0.0029154415,0.0013459809,0.29130787,0.0020358507,0.0016855106,0.040872633],"study_design_scores_gemma":[0.00024897655,0.0011153105,0.555967,0.00009812168,0.0010507125,0.3772644,0.0016888396,0.0018421017,0.049679685,0.0014198628,0.009504454,0.000120519195],"about_ca_topic_score_codex":0.0015655167,"about_ca_topic_score_gemma":0.001097206,"teacher_disagreement_score":0.0024969082,"about_ca_system_score_codex":0.00022763664,"about_ca_system_score_gemma":0.0001924426,"threshold_uncertainty_score":0.008352935},"labels":[],"label_agreement":null},{"id":"W2037046278","doi":"10.1038/ng.446","title":"Twenty bone-mineral-density loci identified by large-scale meta-analysis of genome-wide association studies","year":2009,"lang":"en","type":"review","venue":"Nature Genetics","topic":"Genetic Associations and Epidemiology","field":"Biochemistry, Genetics and Molecular Biology","cited_by":706,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"McGill University and Génome Québec Innovation Centre; McGill University","funders":"National Heart, Lung, and Blood Institute; National Institute on Aging; National Institute of Arthritis and Musculoskeletal and Skin Diseases; Versus Arthritis; European Commission; ZonMw; Canadian Institutes of Health Research; Centre for Medical Systems Biology; National Institute for Health and Care Research; Erasmus Medisch Centrum; Wellcome Trust; Nederlandse Organisatie voor Wetenschappelijk Onderzoek; Ministerie van Onderwijs, Cultuur en Wetenschap","keywords":"Genome-wide association study; Biology; Single-nucleotide polymorphism; Bone mineral; Osteoporosis; Genetics; Quantitative trait locus; Genetic association; SNP; Computational biology; Gene; Endocrinology; Genotype","score_opus":0.038589314803750184,"score_gpt":0.3475557968556903,"score_spread":0.30896648205194016,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2037046278","genre_codex":"review","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":null,"domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.0005255657,0.9982193,0.00054478284,0.00036251792,0.0000865148,0.0000049318137,0.0000703459,0.000015062664,0.00017105608],"genre_scores_gemma":[0.004265373,0.9932412,0.0015073279,0.00043334663,0.00017217107,0.000011195091,0.00019355978,0.0000045963275,0.00017111834],"study_design_codex":"design_other","study_design_gemma":"meta_analysis","domain_scores_codex":[0.9991689,0.00017106278,0.0001435805,0.0002367843,0.00024004084,0.000039800132],"domain_scores_gemma":[0.99635446,0.0025942102,0.0003764507,0.00010422273,0.00046719858,0.00010354656],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0031833851,0.0015235229,0.0040317387,0.0024752144,0.00023178165,0.0012312862,0.0020975082,0.0013044782,0.0012688785],"category_scores_gemma":[0.0046089925,0.0005050356,0.0012744028,0.0043314546,0.00051922345,0.0007801563,0.00080722925,0.0010704909,0.000755842],"study_design_candidate":"meta_analysis","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00044738883,0.000053791027,0.005883797,0.019013291,0.0040925182,0.0006050671,0.000051396677,0.0004434934,0.0018253081,0.0008738743,0.016239373,0.9504707],"study_design_scores_gemma":[0.0011003799,0.00096261094,0.11002758,0.023237247,0.0408899,0.01662634,0.0004952944,0.0013364503,0.0062251,0.01741703,0.7811995,0.00048251302],"about_ca_topic_score_codex":0.0019975235,"about_ca_topic_score_gemma":0.005854749,"teacher_disagreement_score":0.0040317387,"about_ca_system_score_codex":0.0006221869,"about_ca_system_score_gemma":0.001954275,"threshold_uncertainty_score":0.01683551},"labels":[],"label_agreement":null},{"id":"W2037656814","doi":"10.1038/ng1420","title":"Heterozygous deletion of the linked genes ZIC1 and ZIC4 is involved in Dandy-Walker malformation","year":2004,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Fetal and Pediatric Neurological Disorders","field":"Medicine","cited_by":250,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"London Health Sciences Centre","funders":"Brain Research Foundation","keywords":"Biology; Phenotype; Genetics; Gene; Zinc finger; Cerebellum; Neuroscience; Transcription factor","score_opus":0.010577923152695437,"score_gpt":0.23990568358564907,"score_spread":0.22932776043295364,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2037656814","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9971558,0.00035060468,0.0011245367,0.00008671787,0.000014441817,0.000011013611,0.00027832194,0.000049760136,0.0009288252],"genre_scores_gemma":[0.9981572,0.00016691469,0.0008186721,0.000020592064,0.000010372308,0.0000075420867,0.00020092227,0.000014556897,0.0006031693],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9998223,0.00002709903,0.000021563423,0.000039528404,0.00006125368,0.00002824892],"domain_scores_gemma":[0.9996712,0.00012717473,0.00011304942,0.000016313392,0.000013224299,0.000058936002],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.000113785856,0.0005448374,0.0003555135,0.0011576738,0.00029397255,0.00023849601,0.00058313593,0.0006599517,0.0025814297],"category_scores_gemma":[0.0006578621,0.0002836802,0.00015778883,0.0004916307,0.0005638121,0.00014209801,0.00033926492,0.00048196156,0.00033360271],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0013475948,0.00012182768,0.025601516,0.00012859765,0.00012914899,0.06071623,0.00023416571,0.0007814774,0.8964321,0.00158758,0.00063598953,0.012283742],"study_design_scores_gemma":[0.00049485377,0.0005545832,0.37547734,0.000059263162,0.0007363834,0.25217542,0.0005612623,0.005610675,0.354986,0.00249983,0.006760776,0.00008355948],"about_ca_topic_score_codex":0.0013336506,"about_ca_topic_score_gemma":0.0012833672,"teacher_disagreement_score":0.0025814297,"about_ca_system_score_codex":0.00018784632,"about_ca_system_score_gemma":0.00021611666,"threshold_uncertainty_score":0.0086357},"labels":[],"label_agreement":null},{"id":"W2038309633","doi":"10.1038/ng.693","title":"Genome-wide association analysis identifies three psoriasis susceptibility loci","year":2010,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Psoriasis: Treatment and Pathogenesis","field":"Immunology and Microbiology","cited_by":336,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Toronto; Memorial University of Newfoundland","funders":"National Institute of Arthritis and Musculoskeletal and Skin Diseases; National Human Genome Research Institute; Canadian Institutes of Health Research","keywords":"Biology; Genome-wide association study; Psoriasis; Genetics; Genetic association; Meta-analysis; Single-nucleotide polymorphism; Genotype; Internal medicine; Gene; Immunology; Medicine","score_opus":0.008543461758992255,"score_gpt":0.24153603719323627,"score_spread":0.232992575434244,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2038309633","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9941883,0.0008863092,0.0027756197,0.0005185827,0.000031972897,0.00001414085,0.00041556943,0.00007189917,0.001097547],"genre_scores_gemma":[0.9980927,0.00017081987,0.0011246877,0.00008139585,0.000017962248,0.0000064422734,0.00022336937,0.000014744908,0.00026788146],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99916065,0.00022891282,0.00006917709,0.0002557421,0.00017097166,0.00011459681],"domain_scores_gemma":[0.998431,0.0007275445,0.00037659294,0.00013025706,0.00010450979,0.0002301193],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00088565936,0.0006067461,0.00055172876,0.001749717,0.0006610366,0.0009392058,0.00075052277,0.0011381843,0.0027634245],"category_scores_gemma":[0.0013397621,0.0003616547,0.0010413403,0.0018854575,0.0007749906,0.00021101681,0.0005101191,0.0012526984,0.0003129686],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.009453729,0.000696531,0.64138454,0.0001920636,0.0022751428,0.0045233523,0.0006147864,0.0007163244,0.3047943,0.0019057231,0.0017990156,0.03164447],"study_design_scores_gemma":[0.00032264335,0.00031619167,0.98133963,0.000023007922,0.0012634178,0.003296215,0.00021581244,0.0012114869,0.009497428,0.0011531054,0.0013245071,0.000036567897],"about_ca_topic_score_codex":0.0028992419,"about_ca_topic_score_gemma":0.003336211,"teacher_disagreement_score":0.0028992419,"about_ca_system_score_codex":0.0002674989,"about_ca_system_score_gemma":0.0004441733,"threshold_uncertainty_score":0.009244561},"labels":[],"label_agreement":null},{"id":"W2038732878","doi":"10.1038/ng.2252","title":"ISPD loss-of-function mutations disrupt dystroglycan O-mannosylation and cause Walker-Warburg syndrome","year":2012,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Muscle Physiology and Disorders","field":"Biochemistry, Genetics and Molecular Biology","cited_by":239,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Hospital for Sick Children","funders":"National Institute of Diabetes and Digestive and Kidney Diseases; Rosetrees Trust; National Institute of Arthritis and Musculoskeletal and Skin Diseases; National Institute of Neurological Disorders and Stroke; Howard Hughes Medical Institute","keywords":"Complementation; Biology; Protein-fragment complementation assay; Congenital muscular dystrophy; Genetics; Dystroglycan; Mutation; Phenotype; Loss function; Gene; Laminin; Cell","score_opus":0.007264604837405344,"score_gpt":0.2621231578588109,"score_spread":0.2548585530214056,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2038732878","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9925538,0.00043209398,0.003453625,0.00017009075,0.00006277964,0.000032094773,0.00062057347,0.0001727029,0.0025022605],"genre_scores_gemma":[0.9963433,0.00028748545,0.0015387306,0.000058486923,0.000021783677,0.000020425694,0.00037989434,0.00006298226,0.0012868898],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99984527,0.000023377228,0.00003342673,0.000023857316,0.000048894883,0.00002526469],"domain_scores_gemma":[0.9997298,0.000056978628,0.000097102755,0.00002014265,0.000010619878,0.000085312735],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.000124411,0.0015946317,0.00039659577,0.0010053747,0.0004108932,0.00048667437,0.0006332117,0.00085250934,0.0026195329],"category_scores_gemma":[0.00035753427,0.0003967268,0.00046621528,0.00066133746,0.0010348439,0.00027194113,0.00076333305,0.0008415911,0.0009382854],"study_design_candidate":"bench_or_experimental","study_design_consensus":"bench_or_experimental","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0006254547,0.00019465918,0.0054244194,0.00012566609,0.00013447524,0.02223095,0.00017753203,0.0016986331,0.9579402,0.0020389925,0.001017536,0.0083913915],"study_design_scores_gemma":[0.000348271,0.000513459,0.052890055,0.000060408325,0.0005085768,0.0625838,0.00034000154,0.009010055,0.8586419,0.0018339173,0.013187568,0.000081960454],"about_ca_topic_score_codex":0.0012122189,"about_ca_topic_score_gemma":0.001877603,"teacher_disagreement_score":0.0026195329,"about_ca_system_score_codex":0.00049737917,"about_ca_system_score_gemma":0.00041921146,"threshold_uncertainty_score":0.008763194},"labels":[],"label_agreement":null},{"id":"W2038934448","doi":"10.1038/ng1506","title":"Human telomeric protein TRF2 associates with genomic double-strand breaks as an early response to DNA damage","year":2005,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Telomeres, Telomerase, and Senescence","field":"Medicine","cited_by":215,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Toronto; Hospital for Sick Children","funders":"","keywords":"Ku70; Biology; DNA damage; Rad50; Telomere; Cell biology; DNA repair; Genome instability; DNA; Nijmegen breakage syndrome; Molecular biology; Telomere-binding protein; MYB; Genetics; DNA-binding protein; Gene; Transcription factor","score_opus":0.009996362940141973,"score_gpt":0.2828303004245901,"score_spread":0.2728339374844482,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2038934448","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9770181,0.015361644,0.0036899252,0.00035637105,0.00016593914,0.000043225642,0.0005715929,0.00025967884,0.0025335066],"genre_scores_gemma":[0.9873139,0.0023280303,0.0017562415,0.00014635184,0.00009965255,0.000052803167,0.0020871654,0.000040869836,0.006175023],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99980575,0.000025347505,0.0000072459525,0.000042224474,0.00006589972,0.000053514512],"domain_scores_gemma":[0.9997876,0.000028873015,0.000046319794,0.00002836997,0.000034010343,0.00007483971],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00029226174,0.00051512104,0.00038854344,0.00061141694,0.00033849472,0.00060793455,0.000247946,0.0005231575,0.0015587222],"category_scores_gemma":[0.00035437196,0.0003135519,0.00046494885,0.00028220942,0.00025761806,0.00028437504,0.0003763443,0.0007236387,0.00092292513],"study_design_candidate":"bench_or_experimental","study_design_consensus":"bench_or_experimental","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0003979157,0.000048184636,0.0011657987,0.00004550055,0.000017900606,0.00021718694,0.000025109633,0.000057953952,0.9956868,0.00007187046,0.00038405615,0.0018816914],"study_design_scores_gemma":[0.0000834524,0.00046404536,0.093240395,0.000027421389,0.00004901948,0.0021552905,0.00010698592,0.0011764726,0.8926351,0.00022986355,0.0098084705,0.000023472034],"about_ca_topic_score_codex":0.0004965691,"about_ca_topic_score_gemma":0.0008216422,"teacher_disagreement_score":0.0015587222,"about_ca_system_score_codex":0.00042443973,"about_ca_system_score_gemma":0.00014940184,"threshold_uncertainty_score":0.0052144527},"labels":[],"label_agreement":null},{"id":"W2039030772","doi":"10.1038/ng888","title":"Oncogenic properties of PPM1D located within a breast cancer amplification epicenter at 17q23","year":2002,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Cancer-related Molecular Pathways","field":"Medicine","cited_by":249,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Ontario Genomics","funders":"National Cancer Institute","keywords":"Biology; Epicenter; Gene duplication; Phenotype; Serine; Gene; Cancer research; Apoptosis; Genetics; Cancer; Breast cancer; Malignant transformation; Threonine; Molecular biology; Phosphorylation","score_opus":0.020421796218625585,"score_gpt":0.2487901154276628,"score_spread":0.22836831920903722,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2039030772","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9977054,0.0003308374,0.00047359458,0.00009590135,0.000015407135,0.000008866629,0.00021010781,0.000016825601,0.0011429271],"genre_scores_gemma":[0.99917334,0.000100002544,0.00027906176,0.000016856673,0.0000041968465,0.000005976492,0.00016484801,0.0000046069254,0.00025107976],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.999859,0.000020239611,0.000013389882,0.00003111861,0.00004152368,0.00003478242],"domain_scores_gemma":[0.9997702,0.000092320166,0.000055914115,0.00002640672,0.000016711992,0.000038439946],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00016701706,0.00018405254,0.00025387568,0.00065862807,0.00031404043,0.0003118395,0.00028486105,0.00031844096,0.0021525002],"category_scores_gemma":[0.0004786448,0.00019878983,0.00026245342,0.0003704198,0.0004019057,0.00013959548,0.00046350667,0.00040534785,0.000328361],"study_design_candidate":"bench_or_experimental","study_design_consensus":"bench_or_experimental","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0010235048,0.000064354266,0.019618621,0.00006689718,0.00006153267,0.009859317,0.00013047017,0.00067498774,0.9620379,0.00070322223,0.00024145616,0.0055176048],"study_design_scores_gemma":[0.00022227045,0.0008747922,0.17896256,0.000023807932,0.00027824566,0.05137451,0.0004677632,0.0032905664,0.75407106,0.00072155736,0.009684698,0.000028105942],"about_ca_topic_score_codex":0.0014774301,"about_ca_topic_score_gemma":0.0012678251,"teacher_disagreement_score":0.0021525002,"about_ca_system_score_codex":0.00037421458,"about_ca_system_score_gemma":0.00018005117,"threshold_uncertainty_score":0.007200837},"labels":[],"label_agreement":null},{"id":"W2040612932","doi":"10.1038/ng1161","title":"Mutations in PCSK9 cause autosomal dominant hypercholesterolemia","year":2003,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Cholesterol and Lipid Metabolism","field":"Medicine","cited_by":3011,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Montreal Clinical Research Institute","funders":"Fondation de France; Institut National de la Santé et de la Recherche Médicale; Pfizer","keywords":"PCSK9; Kexin; Biology; Proprotein convertase; Apolipoprotein B; LDL receptor; Familial hypercholesterolemia; Lipoprotein; Locus (genetics); Subtilisin; Genetics; Endocrinology; Gene; Internal medicine; Cholesterol; Biochemistry; Medicine","score_opus":0.014215606818059683,"score_gpt":0.2893054004398091,"score_spread":0.27508979362174946,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2040612932","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9860271,0.0010374803,0.0030523355,0.0013118883,0.00033347125,0.00006139722,0.0008401772,0.0002774206,0.007058769],"genre_scores_gemma":[0.9952146,0.00031188887,0.0010161705,0.0001696131,0.00015355654,0.000009959288,0.00022265919,0.000052753763,0.002848865],"study_design_codex":"case_report","study_design_gemma":"observational","domain_scores_codex":[0.99968183,0.000035932808,0.000048383048,0.0000596433,0.00012218839,0.00005206489],"domain_scores_gemma":[0.9994935,0.00015337647,0.00015169183,0.000025584744,0.000045043987,0.0001308087],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00017588622,0.0019302829,0.00064026326,0.0012054512,0.0008991058,0.0004767703,0.0006485497,0.002034788,0.004071582],"category_scores_gemma":[0.00078161893,0.00038279445,0.00079307816,0.0011008941,0.0009183839,0.00024703896,0.00069162325,0.0009255171,0.0010708536],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0024218392,0.00025111256,0.057526372,0.00017589379,0.00054606533,0.5561067,0.0007617382,0.00089330494,0.3541084,0.0031081315,0.0040371246,0.020063289],"study_design_scores_gemma":[0.000653231,0.00070359174,0.2176692,0.00010157081,0.0010985556,0.6429182,0.0006336273,0.004264164,0.11094561,0.002163795,0.018687427,0.0001609244],"about_ca_topic_score_codex":0.003627413,"about_ca_topic_score_gemma":0.00452569,"teacher_disagreement_score":0.004071582,"about_ca_system_score_codex":0.00065398193,"about_ca_system_score_gemma":0.00045040462,"threshold_uncertainty_score":0.013620853},"labels":[],"label_agreement":null},{"id":"W2040671431","doi":"10.1038/ng1219","title":"Huntingtin interacts with REST/NRSF to modulate the transcription of NRSE-controlled neuronal genes","year":2003,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Genetic Neurodegenerative Diseases","field":"Neuroscience","cited_by":934,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of British Columbia","funders":"","keywords":"Huntingtin; Biology; Transcription factor; Huntington's disease; Huntingtin Protein; Repressor; Genetics; Gene silencing; Transcription (linguistics); Cell biology; Gene; Mutant; Internal medicine; Medicine","score_opus":0.015985198234497695,"score_gpt":0.25911380161365605,"score_spread":0.24312860337915834,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2040671431","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.991795,0.0020461916,0.0029651287,0.00012256623,0.000046235175,0.00000751603,0.0001752649,0.00012132664,0.002720911],"genre_scores_gemma":[0.99377656,0.00041124,0.0014051718,0.00013829533,0.000016691762,0.000009277226,0.00055608567,0.000058012803,0.0036286926],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9997937,0.000035850087,0.000013763461,0.000050357226,0.00004528368,0.0000610587],"domain_scores_gemma":[0.999801,0.000045945264,0.000039116447,0.00003710014,0.00002404637,0.00005281841],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0002238123,0.00030389073,0.00030211586,0.00016892604,0.0002666268,0.0005387777,0.00026402556,0.00024985755,0.0013745223],"category_scores_gemma":[0.00021695532,0.0002513629,0.0003955627,0.0001012295,0.00035120116,0.00020702582,0.00039194908,0.00050527614,0.0005353344],"study_design_candidate":"bench_or_experimental","study_design_consensus":"bench_or_experimental","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00016822253,0.000011467793,0.0005260089,0.000012334807,0.000009038645,0.0000879811,0.000022030796,0.00005101745,0.99778324,0.000107326574,0.00008013819,0.0011413242],"study_design_scores_gemma":[0.000053541367,0.00027569974,0.046401523,0.000017121729,0.00003346554,0.00057839626,0.00014156377,0.0026992103,0.9453919,0.00030147753,0.0040893964,0.000016628723],"about_ca_topic_score_codex":0.0010774061,"about_ca_topic_score_gemma":0.0037464742,"teacher_disagreement_score":0.0013745223,"about_ca_system_score_codex":0.00047534498,"about_ca_system_score_gemma":0.00012834724,"threshold_uncertainty_score":0.0045982003},"labels":[],"label_agreement":null},{"id":"W2040964350","doi":"10.1038/ng.2608","title":"A meta-analysis identifies new loci associated with body mass index in individuals of African ancestry","year":2013,"lang":"en","type":"review","venue":"Nature Genetics","topic":"Genetic Associations and Epidemiology","field":"Biochemistry, Genetics and Molecular Biology","cited_by":257,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Université de Montréal; Montreal Heart Institute","funders":"Eunice Kennedy Shriver National Institute of Child Health and Human Development; National Institute on Minority Health and Health Disparities; National Center for Research Resources; U.S. National Library of Medicine; National Institute of Environmental Health Sciences; National Institute of Arthritis and Musculoskeletal and Skin Diseases; National Institute of Allergy and Infectious Diseases; National Institute of Neurological Disorders and Stroke; National Institute of General Medical Sciences; National Center for Advancing Translational Sciences; National Human Genome Research Institute; National Institute of Diabetes and Digestive and Kidney Diseases; National Heart, Lung, and Blood Institute; U.S. Public Health Service; National Institute on Aging; National Cancer Institute; National Institutes of Health","keywords":"Genome-wide association study; Biology; Genetic genealogy; Body mass index; Genetics; Locus (genetics); Ancestry-informative marker; Genotyping; Single-nucleotide polymorphism; Genetic association; Meta-analysis; Demography; Genotype; Population; Medicine; Internal medicine; Gene","score_opus":0.06504058406977173,"score_gpt":0.34379937299827823,"score_spread":0.2787587889285065,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2040964350","genre_codex":"review","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":null,"domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.0027035042,0.9951108,0.00057176803,0.0008370514,0.00019422562,0.0000049774894,0.00018688064,0.000010615402,0.00038008043],"genre_scores_gemma":[0.025183327,0.9711393,0.001392056,0.00091092626,0.0006896657,0.00001685785,0.0003303649,0.000006828032,0.0003307314],"study_design_codex":"design_other","study_design_gemma":"meta_analysis","domain_scores_codex":[0.9994529,0.00015508181,0.00007953102,0.00015988215,0.00011997859,0.000032607917],"domain_scores_gemma":[0.9982956,0.0012305104,0.0002122681,0.00006164865,0.00014903951,0.000051001996],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00193089,0.0010140438,0.0019523686,0.0014487844,0.00014170642,0.0008607001,0.00090023223,0.0010437269,0.0013681087],"category_scores_gemma":[0.003211423,0.00032842797,0.0015433001,0.002403635,0.00031920482,0.00048246075,0.0006144081,0.0010126295,0.0002059047],"study_design_candidate":"meta_analysis","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0015422966,0.00007322863,0.06334821,0.029745044,0.026193818,0.0012255391,0.000112354326,0.0009171172,0.0020722446,0.0020598904,0.02020219,0.85250807],"study_design_scores_gemma":[0.0011231535,0.00082063436,0.3759797,0.029856477,0.12813422,0.011422475,0.00052965496,0.0017052494,0.0030028294,0.018201334,0.42889276,0.0003315732],"about_ca_topic_score_codex":0.0022523939,"about_ca_topic_score_gemma":0.005595057,"teacher_disagreement_score":0.0022523939,"about_ca_system_score_codex":0.00036101553,"about_ca_system_score_gemma":0.0008843935,"threshold_uncertainty_score":0.010211647},"labels":[],"label_agreement":null},{"id":"W2041425187","doi":"10.1038/ng.476","title":"Etv4 and Etv5 are required downstream of GDNF and Ret for kidney branching morphogenesis","year":2009,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Renal and related cancers","field":"Biochemistry, Genetics and Molecular Biology","cited_by":233,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"McMaster University","funders":"National Institute of Diabetes and Digestive and Kidney Diseases; Suomen Kulttuurirahasto","keywords":"Biology; Ureteric bud; Kidney development; Glial cell line-derived neurotrophic factor; Proto-Oncogene Proteins c-ret; Transcription factor; Cell biology; Morphogenesis; ETS transcription factor family; Receptor tyrosine kinase; Genetics; Neurotrophic factors; Cancer research; Signal transduction; Gene; Receptor; Embryonic stem cell","score_opus":0.004303135541266857,"score_gpt":0.2394340688751265,"score_spread":0.23513093333385965,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2041425187","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.98854697,0.0018513073,0.005376097,0.0002490818,0.000055944958,0.000017300126,0.00062310277,0.00011390382,0.0031662153],"genre_scores_gemma":[0.99187356,0.00029161677,0.0027350497,0.00008472324,0.0000075361913,0.000009661741,0.0008440022,0.000052535517,0.004101303],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9997415,0.00004062321,0.000023354347,0.000045850742,0.000081511804,0.00006713879],"domain_scores_gemma":[0.99978465,0.000037987982,0.00007352029,0.000023969897,0.00002280528,0.00005715352],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00018738372,0.00034058923,0.00022999958,0.00038282658,0.00032377554,0.0007989468,0.00053816254,0.00070897926,0.0025786785],"category_scores_gemma":[0.00030238615,0.0004536899,0.00035292952,0.00015667925,0.0003802824,0.0004918332,0.00046199412,0.00081860804,0.0005952995],"study_design_candidate":"bench_or_experimental","study_design_consensus":"bench_or_experimental","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00021709931,0.000008546176,0.0005123737,0.000021326447,0.000007807742,0.00017910429,0.000010754243,0.00024645214,0.99715096,0.0007385855,0.000058346955,0.0008486255],"study_design_scores_gemma":[0.000027984524,0.000051145682,0.011170771,0.0000059115264,0.00002117744,0.00084324693,0.00006424142,0.002208776,0.9811936,0.00038037778,0.0040219044,0.000010916807],"about_ca_topic_score_codex":0.0022798704,"about_ca_topic_score_gemma":0.0033390294,"teacher_disagreement_score":0.0025786785,"about_ca_system_score_codex":0.001124097,"about_ca_system_score_gemma":0.00041389334,"threshold_uncertainty_score":0.008626521},"labels":[],"label_agreement":null},{"id":"W2041653784","doi":"10.1038/ng.2986","title":"Identification of recurrent SMO and BRAF mutations in ameloblastomas","year":2014,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Hedgehog Signaling Pathway Studies","field":"Biochemistry, Genetics and Molecular Biology","cited_by":361,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of British Columbia","funders":"National Cancer Institute; University of British Columbia; Howard Hughes Medical Institute","keywords":"Smoothened; Ameloblastoma; Biology; Cancer research; Vemurafenib; Hedgehog signaling pathway; Hedgehog; Arsenic trioxide; Mutation; Patched; Genetics; Melanoma; Signal transduction; Maxilla; Gene","score_opus":0.00700579065259511,"score_gpt":0.2672113056929366,"score_spread":0.2602055150403415,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2041653784","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99868685,0.0002239224,0.00035258205,0.000022586499,0.0000054838843,0.000006982579,0.000087850065,0.000020520045,0.0005931993],"genre_scores_gemma":[0.9991885,0.00009679386,0.00031164853,0.0000067383135,0.000004741873,0.0000045394913,0.00008937408,0.000008409152,0.00028923916],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.99965346,0.000028223416,0.000051972336,0.000052347197,0.00012458743,0.00008945576],"domain_scores_gemma":[0.99960047,0.00009262547,0.00009921809,0.000062299296,0.00006452723,0.00008082559],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0002981926,0.00027553592,0.00031627194,0.0014133125,0.00032244297,0.00041713522,0.0004270947,0.0004484261,0.0012806564],"category_scores_gemma":[0.0008390837,0.0002994647,0.00037968525,0.00044941055,0.0004039222,0.00026130365,0.00052576646,0.0002921684,0.00041538567],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0008226133,0.000060697275,0.039081145,0.000051532323,0.000050961975,0.0062702186,0.00020628895,0.00014233592,0.9442627,0.00055752177,0.000107608656,0.0083863465],"study_design_scores_gemma":[0.0000687221,0.0010266223,0.30108148,0.000014810256,0.00027420375,0.080907084,0.0005640089,0.0018951787,0.60924906,0.00069553376,0.0041905786,0.00003275081],"about_ca_topic_score_codex":0.00140171,"about_ca_topic_score_gemma":0.0017765819,"teacher_disagreement_score":0.0014133125,"about_ca_system_score_codex":0.00039086665,"about_ca_system_score_gemma":0.00030153317,"threshold_uncertainty_score":0.0042842627},"labels":[],"label_agreement":null},{"id":"W2041778817","doi":"10.1038/ng.190","title":"PTPRD (protein tyrosine phosphatase receptor type delta) is associated with restless legs syndrome","year":2008,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Restless Legs Syndrome Research","field":"Medicine","cited_by":284,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"McGill University; Douglas Mental Health University Institute; Hôpital du Sacré-Cœur de Montréal; Université de Montréal; Hôpital Notre-Dame","funders":"","keywords":"Protein tyrosine phosphatase; Biology; Phosphatase; Delta; Protein phosphatase 2; Receptor; Tyrosine; DUSP6; Genetics; Phosphorylation; Biochemistry","score_opus":0.028205376993859603,"score_gpt":0.30107655152711127,"score_spread":0.27287117453325166,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2041778817","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9949492,0.0008044751,0.0013326625,0.00036403458,0.00010819677,0.00003161741,0.00021879791,0.00006666535,0.0021242853],"genre_scores_gemma":[0.9984578,0.00018068028,0.00038391573,0.00011597,0.00011273208,0.0000091078555,0.00015414294,0.00001610954,0.00056949514],"study_design_codex":"case_report","study_design_gemma":"observational","domain_scores_codex":[0.99949515,0.00011321367,0.0000849392,0.00012457233,0.000099602556,0.00008248575],"domain_scores_gemma":[0.99880135,0.00044394698,0.00035748768,0.00006229628,0.00007304111,0.00026198715],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00032298258,0.0016672577,0.0007928605,0.0020196135,0.0008044377,0.0005881652,0.0009599243,0.0022952536,0.003254135],"category_scores_gemma":[0.0019087691,0.0004512678,0.0008380657,0.0014189382,0.0010060119,0.0004510889,0.0007274044,0.0009812897,0.0005790394],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0012654704,0.00020074616,0.09623632,0.00015263502,0.00031167403,0.8222493,0.00055855745,0.00028462507,0.07167238,0.0006295406,0.0008409755,0.005597683],"study_design_scores_gemma":[0.00021156459,0.00053056376,0.21446781,0.000047523044,0.00048399638,0.7724478,0.00034014936,0.0012544127,0.007727192,0.00051011797,0.0019249651,0.00005387835],"about_ca_topic_score_codex":0.0011643725,"about_ca_topic_score_gemma":0.00075466844,"teacher_disagreement_score":0.003254135,"about_ca_system_score_codex":0.00031401258,"about_ca_system_score_gemma":0.0002308725,"threshold_uncertainty_score":0.010886192},"labels":[],"label_agreement":null},{"id":"W2042259764","doi":"10.1038/ng0604-543","title":"A public gene trap resource for mouse functional genomics","year":2004,"lang":"en","type":"letter","venue":"Nature Genetics","topic":"CRISPR and Genetic Engineering","field":"Biochemistry, Genetics and Molecular Biology","cited_by":212,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Toronto; University of Manitoba","funders":"University of Toronto; Wellcome Trust","keywords":"Biology; GenBank; Genome; Gene; Genetics; Functional genomics; Genomic library; Genomics; Computational biology","score_opus":0.013541120888250052,"score_gpt":0.25482370246541186,"score_spread":0.24128258157716181,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2042259764","genre_codex":"methods","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":null,"domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.007964531,0.060084663,0.29563034,0.26449287,0.050245617,0.004177206,0.018213103,0.03918105,0.2600106],"genre_scores_gemma":[0.04338987,0.061104562,0.25894812,0.14905286,0.019613199,0.009565084,0.04749724,0.0056045046,0.40522447],"study_design_codex":"not_applicable","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9978848,0.00044312398,0.00017402702,0.00017812525,0.0011645228,0.00015546365],"domain_scores_gemma":[0.99809617,0.00051724893,0.00014028346,0.0005448175,0.00032179075,0.00037960173],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0028485844,0.0011722512,0.0012650851,0.0014670019,0.0013080543,0.002027088,0.0034131052,0.0053573474,0.03613297],"category_scores_gemma":[0.002856507,0.00085496285,0.0006533378,0.0012306689,0.0009441814,0.0016916309,0.0017872773,0.007085055,0.06625533],"study_design_candidate":"bench_or_experimental","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00023609259,0.000103023835,0.0001705115,0.0003235292,0.000018801406,0.0010779604,0.000043470085,0.00009609501,0.028544087,0.011427319,0.86559916,0.09235995],"study_design_scores_gemma":[0.000087631735,0.00006266133,0.00024552236,0.000075505755,0.000010504127,0.001559187,0.000010149791,0.0004977733,0.004928329,0.0036644635,0.988837,0.000021245018],"about_ca_topic_score_codex":0.00049215235,"about_ca_topic_score_gemma":0.0018369989,"teacher_disagreement_score":0.03613297,"about_ca_system_score_codex":0.0018583932,"about_ca_system_score_gemma":0.0012342933,"threshold_uncertainty_score":0.12087679},"labels":[],"label_agreement":null},{"id":"W2042560956","doi":"10.1038/ng.2985","title":"Large-scale genetic study in East Asians identifies six new loci associated with colorectal cancer risk","year":2014,"lang":"en","type":"review","venue":"Nature Genetics","topic":"Genetic factors in colorectal cancer","field":"Medicine","cited_by":243,"is_retracted":false,"has_abstract":false,"route_ca_aff":false,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"","funders":"Division of Cancer Epidemiology and Genetics, National Cancer Institute; School of Medicine, University of North Carolina at Chapel Hill; National Institute of Diabetes and Digestive and Kidney Diseases; National Cancer Institute; National Human Genome Research Institute; National Heart, Lung, and Blood Institute; National Institute on Aging; National Key Research and Development Program of China; Faculty of Medicine, Memorial University of Newfoundland; Medical Center, University of Pittsburgh; Albert Einstein College of Medicine, Yeshiva University; School of Medicine, Vanderbilt University; School of Medicine, New York University; University of Toronto; Memorial University of Newfoundland; University of Melbourne; Ministry of Education, Culture, Sports, Science and Technology; University of Pittsburgh; Massey University; York University; National Institute of Environmental Health Sciences; Ottawa Hospital Research Institute; Deutsches Krebsforschungszentrum; Japan Society for the Promotion of Science; Case Comprehensive Cancer Center, Case Western Reserve University; Ohio State University; National Research Foundation; Brigham and Women's Hospital; Kaiser Permanente; Massachusetts General Hospital; Case Western Reserve University; National Natural Science Foundation of China; University of Washington; Yeshiva University; National Institutes of Health; University of Southern California; National Research Foundation of Korea; Department of Internal Medicine, University of Utah; Vanderbilt University","keywords":"Biology; Colorectal cancer; Genetics; Scale (ratio); East Asia; Evolutionary biology; Cancer; China; Cartography","score_opus":0.01776826674750292,"score_gpt":0.3235234460308085,"score_spread":0.3057551792833056,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2042560956","genre_codex":"review","genre_gemma":"review","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"review","genre_consensus":"review","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.0015596321,0.99643564,0.0003166055,0.0007063343,0.00016505031,0.000004510419,0.00007065192,0.000010109979,0.0007315627],"genre_scores_gemma":[0.008245326,0.98983055,0.00058610726,0.0005072351,0.00029399814,0.000005942239,0.00012946317,0.000002117062,0.00039922798],"study_design_codex":"design_other","study_design_gemma":"observational","domain_scores_codex":[0.99984205,0.000026298158,0.00002771984,0.000040870487,0.000048314207,0.000014732668],"domain_scores_gemma":[0.99950194,0.00028991073,0.00008426286,0.000013549224,0.00007377923,0.000036598398],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0005075161,0.0006539349,0.0010319778,0.0010571484,0.00012826527,0.00051594933,0.0006528638,0.0006980797,0.0013143816],"category_scores_gemma":[0.0008767362,0.0001719771,0.0005359453,0.001461743,0.00030191286,0.00040994832,0.00041769928,0.00086161785,0.0002904509],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0002755617,0.000068163325,0.015526077,0.01159242,0.0011220524,0.001211644,0.00008625564,0.00040806946,0.0033229282,0.0018754993,0.016343076,0.9481683],"study_design_scores_gemma":[0.00026236536,0.00034588858,0.105060436,0.010351745,0.007491839,0.009861467,0.00049624156,0.0005136933,0.002964302,0.0078075943,0.8546889,0.00015555488],"about_ca_topic_score_codex":0.00190151,"about_ca_topic_score_gemma":0.00324497,"teacher_disagreement_score":0.00190151,"about_ca_system_score_codex":0.00031188378,"about_ca_system_score_gemma":0.00083329546,"threshold_uncertainty_score":0.0043970346},"labels":[],"label_agreement":null},{"id":"W2043321552","doi":"10.1038/ng1229","title":"Hermansky-Pudlak syndrome type 7 (HPS-7) results from mutant dysbindin, a member of the biogenesis of lysosome-related organelles complex 1 (BLOC-1)","year":2003,"lang":"en","type":"article","venue":"Nature Genetics","topic":"melanin and skin pigmentation","field":"Biochemistry, Genetics and Molecular Biology","cited_by":432,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Toronto; Mount Sinai Hospital","funders":"National Institute of Allergy and Infectious Diseases; Eunice Kennedy Shriver National Institute of Child Health and Human Development; National Heart, Lung, and Blood Institute; Wellcome Trust; University of Oklahoma","keywords":"Hermansky–Pudlak syndrome; Biology; Lysosome; Biogenesis; Melanosome; Cell biology; Organelle; Organelle biogenesis; Mutant; Mutation; Golgi apparatus; Oculocutaneous albinism; Phenotype; Genetics; Gene; Endoplasmic reticulum; Biochemistry; Pulmonary fibrosis; Melanin; Pathology","score_opus":0.01241476409119673,"score_gpt":0.2499165764236725,"score_spread":0.23750181233247575,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2043321552","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9869292,0.001480993,0.0048864265,0.0004994068,0.0002623253,0.00006223194,0.0011545854,0.00056894537,0.0041557546],"genre_scores_gemma":[0.99158245,0.00077063055,0.0025982293,0.00009950512,0.00007392858,0.000029535146,0.00076741574,0.00012356031,0.003954831],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9995968,0.00004383387,0.000043967677,0.000079020465,0.0001924837,0.000043918222],"domain_scores_gemma":[0.99938786,0.00010412224,0.0002574599,0.000028972163,0.000029564135,0.00019205753],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00017969118,0.0017106876,0.0004465635,0.0013388869,0.0005022661,0.00045869403,0.0007028262,0.0012330548,0.0028693432],"category_scores_gemma":[0.000577292,0.00046482054,0.00048061827,0.00049990276,0.0015107882,0.00035732525,0.0012042365,0.0011448856,0.0009038773],"study_design_candidate":"bench_or_experimental","study_design_consensus":"bench_or_experimental","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.001135216,0.00018145415,0.005118352,0.00025975058,0.00028479143,0.04201627,0.00021658561,0.0008022921,0.93042946,0.004673888,0.0024356404,0.012446216],"study_design_scores_gemma":[0.0009305059,0.0010297258,0.10955798,0.00013959725,0.0007247963,0.18770722,0.00047534204,0.0053183185,0.65957063,0.0065361653,0.027814144,0.0001955919],"about_ca_topic_score_codex":0.0010818811,"about_ca_topic_score_gemma":0.0016335703,"teacher_disagreement_score":0.0028693432,"about_ca_system_score_codex":0.0005868512,"about_ca_system_score_gemma":0.00058239774,"threshold_uncertainty_score":0.009598911},"labels":[],"label_agreement":null},{"id":"W2043690660","doi":"10.1038/79851","title":"Mutations in GJB6 cause hidrotic ectodermal dysplasia","year":2000,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Connexins and lens biology","field":"Biochemistry, Genetics and Molecular Biology","cited_by":288,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"McGill University; Montreal Children's Hospital; Montreal General Hospital","funders":"","keywords":"Ectodermal dysplasia; Biology; Genetics; Mutation; Gene","score_opus":0.0061650839686986595,"score_gpt":0.2559913986531175,"score_spread":0.24982631468441882,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2043690660","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.98231,0.0027500107,0.0033440157,0.0006440606,0.0002769468,0.000060367212,0.0010611161,0.00032881973,0.0092247045],"genre_scores_gemma":[0.99426067,0.0007499853,0.0015299757,0.00012539657,0.0000762776,0.000015076495,0.00023718373,0.00008521555,0.0029201296],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9996729,0.000053407064,0.000047475416,0.00006402776,0.000106072745,0.000056165773],"domain_scores_gemma":[0.99925953,0.00022290144,0.00022858618,0.000042696218,0.000035099318,0.0002111421],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0001956344,0.0014460669,0.00077988347,0.0014132533,0.0007416943,0.0003531515,0.00050554087,0.0019675798,0.005845924],"category_scores_gemma":[0.0006714547,0.0005252165,0.00038721616,0.00075776863,0.0011208401,0.00036848584,0.0008334261,0.0011115188,0.0013379833],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00081385486,0.0001271016,0.006839422,0.0002568608,0.00021102834,0.14540856,0.00043602477,0.0005500099,0.8338104,0.0020096686,0.0015237253,0.008013262],"study_design_scores_gemma":[0.00036567575,0.00054665585,0.1597976,0.00016565154,0.00072832697,0.5054743,0.0006566339,0.002782863,0.30494225,0.001784009,0.022620004,0.00013600924],"about_ca_topic_score_codex":0.0014920926,"about_ca_topic_score_gemma":0.0026229175,"teacher_disagreement_score":0.005845924,"about_ca_system_score_codex":0.000300437,"about_ca_system_score_gemma":0.0002954519,"threshold_uncertainty_score":0.019556582},"labels":[],"label_agreement":null},{"id":"W2044518560","doi":"10.1038/ng.443","title":"Genetic variant near IRS1 is associated with type 2 diabetes, insulin resistance and hyperinsulinemia","year":2009,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Genetic Associations and Epidemiology","field":"Biochemistry, Genetics and Molecular Biology","cited_by":479,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Université de Montréal; Centre Hospitalier de l’Université de Montréal; McGill University; Diabetes Canada; McGill University and Génome Québec Innovation Centre","funders":"","keywords":"Hyperinsulinemia; Insulin resistance; Biology; Single-nucleotide polymorphism; IRS1; Type 2 diabetes; Insulin receptor; Genome-wide association study; Population; Internal medicine; Endocrinology; Genetics; Insulin; Genetic association; Diabetes mellitus; Gene; Medicine; Genotype","score_opus":0.004817587405573285,"score_gpt":0.2247904397365719,"score_spread":0.21997285233099861,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2044518560","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9981944,0.00028387245,0.00043739972,0.00014020951,0.000044755227,0.000009084991,0.00017208836,0.000026553971,0.0006916621],"genre_scores_gemma":[0.9982292,0.00011732145,0.00055753125,0.000054291817,0.00006429844,0.000009073074,0.000161586,0.00001650379,0.00079027255],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9991949,0.00028722067,0.000109715686,0.0002093159,0.00013033088,0.00006852729],"domain_scores_gemma":[0.99755186,0.000921419,0.00081447425,0.0001763029,0.00014074147,0.00039518985],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0007741481,0.0013524952,0.00076872867,0.0021298078,0.0009760909,0.00072282704,0.00085594144,0.0015880504,0.0044508595],"category_scores_gemma":[0.0025029941,0.0006319143,0.00095950597,0.002263537,0.0006385898,0.00036731508,0.00046131597,0.0015242528,0.0005321116],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.010663577,0.0009679966,0.8945504,0.00016666655,0.0018249302,0.014857123,0.00071504904,0.000600495,0.065062754,0.0007131966,0.0008105639,0.009067221],"study_design_scores_gemma":[0.00025180035,0.00076428097,0.9726433,0.00004859912,0.0008603661,0.018324327,0.00028407847,0.0018802773,0.0034907458,0.00060374755,0.0007933067,0.000055148328],"about_ca_topic_score_codex":0.0019391405,"about_ca_topic_score_gemma":0.0011269399,"teacher_disagreement_score":0.0044508595,"about_ca_system_score_codex":0.00026048478,"about_ca_system_score_gemma":0.00023366637,"threshold_uncertainty_score":0.014889598},"labels":[],"label_agreement":null},{"id":"W2045113343","doi":"10.1038/ng.311","title":"Genome-wide scan reveals association of psoriasis with IL-23 and NF-κB pathways","year":2009,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Psoriasis: Treatment and Pathogenesis","field":"Immunology and Microbiology","cited_by":1396,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Memorial University of Newfoundland; University of Toronto","funders":"National Center for Research Resources; Foundation for the National Institutes of Health; National Institute of Arthritis and Musculoskeletal and Skin Diseases; National Human Genome Research Institute; National Institutes of Health; National Heart, Lung, and Blood Institute","keywords":"Psoriasis; Biology; Genetics; Single-nucleotide polymorphism; Genome-wide association study; Genetic association; Gene; Epistasis; Immune system; Genetic predisposition; Immunology; Genotype","score_opus":0.007429858098225966,"score_gpt":0.21244382661875544,"score_spread":0.20501396852052947,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2045113343","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9938114,0.0021633366,0.00077950634,0.0003209225,0.000021523443,0.000008320373,0.0019852032,0.000051104158,0.00085868035],"genre_scores_gemma":[0.9974069,0.0006053216,0.00051699695,0.00011298952,0.00002085415,0.000010866754,0.00088800356,0.00001661235,0.00042153525],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99958926,0.00009950001,0.00003048054,0.00013851383,0.00008155701,0.000060673196],"domain_scores_gemma":[0.99925524,0.0002746656,0.00023702008,0.00004879827,0.00005308598,0.00013115408],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00038974299,0.00036049174,0.00053085905,0.0009162439,0.0003341951,0.0006587335,0.00037794694,0.00041228198,0.0032036782],"category_scores_gemma":[0.00081270456,0.0002346836,0.0008249277,0.0012260012,0.00029978465,0.00014728171,0.00036828197,0.0006281455,0.00027725537],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.008269246,0.00028255637,0.6320417,0.00036043517,0.004845948,0.0030797694,0.00027330703,0.0008139281,0.31880572,0.00047655636,0.002341386,0.028409544],"study_design_scores_gemma":[0.00012694797,0.00017254685,0.98971444,0.000018841854,0.0011586789,0.0021152429,0.000108837114,0.00048157532,0.0044744085,0.00038256156,0.0012285347,0.0000173475],"about_ca_topic_score_codex":0.0029719337,"about_ca_topic_score_gemma":0.0040322137,"teacher_disagreement_score":0.0032036782,"about_ca_system_score_codex":0.00019326217,"about_ca_system_score_gemma":0.00031245075,"threshold_uncertainty_score":0.010717392},"labels":[],"label_agreement":null},{"id":"W2045227722","doi":"10.1038/ng.2711","title":"Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs","year":2013,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Genetic Associations and Epidemiology","field":"Biochemistry, Genetics and Molecular Biology","cited_by":2353,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Centre for Addiction and Mental Health; Public Health Ontario; University of British Columbia; Hospital for Sick Children; SickKids Foundation; University of Toronto; McGill University","funders":"Eunice Kennedy Shriver National Institute of Child Health and Human Development; Nederlandse Organisatie voor Wetenschappelijk Onderzoek; Wellcome Trust; National Human Genome Research Institute; National Cancer Institute; National Institute on Alcohol Abuse and Alcoholism; National Health and Medical Research Council; National Institute of Mental Health; Medical Research Council; Australian Research Council; Vrije Universiteit Amsterdam; Goddard Space Flight Center; Crohn's and Colitis UK","keywords":"Biology; Single-nucleotide polymorphism; Genome-wide association study; Genetics; Genome; Computational biology; Gene; Genotype","score_opus":0.011139447568889174,"score_gpt":0.26666253950858326,"score_spread":0.2555230919396941,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2045227722","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99795854,0.00024108424,0.000777817,0.00006286816,0.000009742101,0.0000053364693,0.00047260424,0.000011220736,0.0004608081],"genre_scores_gemma":[0.99923074,0.00004754347,0.00032811286,0.000012900745,0.0000056932945,0.0000032183132,0.00025229025,0.0000025733616,0.000116883624],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99912816,0.00028195124,0.00009243869,0.0003123897,0.00008726475,0.00009781524],"domain_scores_gemma":[0.9980477,0.0010543118,0.0004431435,0.0001404705,0.00011750243,0.00019671893],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0008115376,0.00042951215,0.00028839053,0.0015538231,0.00054332515,0.00064945983,0.00040063422,0.0006268982,0.003551581],"category_scores_gemma":[0.0026940242,0.00025356535,0.00073713204,0.0013237195,0.00042964812,0.00026414817,0.0006004972,0.00077175425,0.0002471954],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0009379051,0.00004910851,0.9870122,0.00002314694,0.00082684704,0.00033549205,0.00012250058,0.00036288818,0.0071536126,0.0002518516,0.00010612669,0.002818329],"study_design_scores_gemma":[0.000029648121,0.00010064746,0.99674326,0.000007703287,0.00043374157,0.00055260793,0.0001149178,0.0007628448,0.0006830725,0.0003612101,0.00020101955,0.000009313887],"about_ca_topic_score_codex":0.004938592,"about_ca_topic_score_gemma":0.0039724186,"teacher_disagreement_score":0.004938592,"about_ca_system_score_codex":0.00025801797,"about_ca_system_score_gemma":0.0002678797,"threshold_uncertainty_score":0.011881173},"labels":[],"label_agreement":null},{"id":"W2045731124","doi":"10.1038/ng1206-1360","title":"A new piece in the nephrotic puzzle","year":2006,"lang":"en","type":"letter","venue":"Nature Genetics","topic":"Renal Diseases and Glomerulopathies","field":"Medicine","cited_by":9,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Toronto; Mount Sinai Hospital","funders":"","keywords":"Biology; Nephrotic syndrome; Genetics; Computational biology; Evolutionary biology; Endocrinology","score_opus":0.008031082916688562,"score_gpt":0.25759536048002474,"score_spread":0.24956427756333618,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2045731124","genre_codex":"commentary","genre_gemma":"commentary","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"commentary","genre_consensus":"commentary","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.0006223491,0.005893382,0.00017290756,0.97692704,0.014849146,0.0000032664223,0.000012739043,0.000017562099,0.0015015473],"genre_scores_gemma":[0.013183786,0.007884694,0.0006038366,0.85938394,0.11402564,0.000016391774,0.000020887806,0.000022041437,0.0048587676],"study_design_codex":"not_applicable","study_design_gemma":"not_applicable","domain_scores_codex":[0.99840456,0.00072642736,0.0001640408,0.00016096633,0.00037609992,0.0001679966],"domain_scores_gemma":[0.99468553,0.003698451,0.0001955474,0.00018569242,0.000607692,0.0006270552],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0028548872,0.0006988292,0.0016048171,0.0006319944,0.002322243,0.002524089,0.001244067,0.025105322,0.004186695],"category_scores_gemma":[0.012496565,0.00040382883,0.0007137736,0.0003903184,0.0036907448,0.0053386963,0.0015602064,0.024335986,0.0016734694],"study_design_candidate":"not_applicable","study_design_consensus":"not_applicable","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00024044915,0.00008470379,0.0012133396,0.0001901948,0.000050842802,0.007899943,0.00029903642,0.0001856715,0.0005875987,0.011929496,0.9424733,0.034845445],"study_design_scores_gemma":[0.00037896313,0.00013707514,0.001723774,0.00044762387,0.00006447317,0.012548835,0.00083875743,0.0008395533,0.0003575258,0.05851467,0.92405903,0.00008981681],"about_ca_topic_score_codex":0.00088426337,"about_ca_topic_score_gemma":0.002372868,"teacher_disagreement_score":0.025105322,"about_ca_system_score_codex":0.0015594481,"about_ca_system_score_gemma":0.0011594015,"threshold_uncertainty_score":0.015098274},"labels":[],"label_agreement":null},{"id":"W2045784260","doi":"10.1038/87232","title":"Identification of genes that are differentially expressed in response to EGF receptor signaling in A549 lung cancer cells using a combination of suppression subtractive hybridization and microarrays","year":2001,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Gene expression and cancer classification","field":"Biochemistry, Genetics and Molecular Biology","cited_by":0,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Biotechnology Research Institute","funders":"","keywords":"Suppression subtractive hybridization; Biology; Identification (biology); DNA microarray; Lung cancer; Gene; Cancer research; Computational biology; Signal transduction; Genetics; Molecular biology; Gene expression; cDNA library; Pathology","score_opus":0.01175108074963365,"score_gpt":0.2861428104504901,"score_spread":0.27439172970085646,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2045784260","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.98161745,0.0023259446,0.008921687,0.00026814395,0.00009189388,0.00008920015,0.003981469,0.00016579845,0.0025385942],"genre_scores_gemma":[0.96815264,0.0019293743,0.013912349,0.00026321627,0.000050695424,0.00024530222,0.008707392,0.000059998827,0.006679013],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99971455,0.00002468009,0.000025617752,0.00006998987,0.00009723091,0.000067905115],"domain_scores_gemma":[0.9998325,0.000051716805,0.0000292392,0.000017402073,0.00003458358,0.00003459278],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00021665082,0.00035483428,0.000666058,0.00062587764,0.00041756846,0.0004811851,0.00023483807,0.00036940348,0.00088400225],"category_scores_gemma":[0.00017982796,0.00024627746,0.00052420923,0.0006608287,0.00029991328,0.0001984527,0.00019761227,0.0006354195,0.0004685366],"study_design_candidate":"bench_or_experimental","study_design_consensus":"bench_or_experimental","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00007684626,0.000010619321,0.00030573877,0.000015978081,0.0000041643925,0.00002435644,0.0000130944545,0.000020876563,0.99899036,0.000033039916,0.000026460406,0.00047848813],"study_design_scores_gemma":[0.000024089944,0.00020349544,0.053834055,0.0000075115845,0.0000679101,0.00051315676,0.00014625113,0.0014933023,0.9406651,0.00011101471,0.00292077,0.000013228302],"about_ca_topic_score_codex":0.0015956258,"about_ca_topic_score_gemma":0.0028091993,"teacher_disagreement_score":0.0015956258,"about_ca_system_score_codex":0.0003403818,"about_ca_system_score_gemma":0.00032211942,"threshold_uncertainty_score":0.003172636},"labels":[],"label_agreement":null},{"id":"W2046702406","doi":"10.1038/ng0407-425","title":"A database of locus-specific databases","year":2007,"lang":"en","type":"letter","venue":"Nature Genetics","topic":"Genomic variations and chromosomal abnormalities","field":"Biochemistry, Genetics and Molecular Biology","cited_by":54,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"McGill University Health Centre; Montreal Children's Hospital","funders":"National Health and Medical Research Council; Medical Research Council; March of Dimes Foundation","keywords":"Biology; Database; Locus (genetics); Genetics; Computational biology; Gene; Computer science","score_opus":0.015588499780278382,"score_gpt":0.25719723371263364,"score_spread":0.24160873393235527,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2046702406","genre_codex":"dataset","genre_gemma":"other","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"other","genre_consensus":null,"domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.01928325,0.021375075,0.28318676,0.08978428,0.01467727,0.0012671591,0.41888005,0.055129603,0.09641656],"genre_scores_gemma":[0.045754258,0.016465237,0.24738781,0.02041463,0.004304356,0.0010482483,0.62011826,0.004208481,0.040298644],"study_design_codex":"not_applicable","study_design_gemma":"not_applicable","domain_scores_codex":[0.9992944,0.000106206244,0.00017721555,0.00012934096,0.00023263464,0.000060101203],"domain_scores_gemma":[0.9931292,0.0023115287,0.00035410633,0.0017256128,0.0015362583,0.0009432489],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0017880474,0.0006884817,0.0012365839,0.0038900042,0.0007591155,0.0028189605,0.0022493182,0.0019125983,0.033831142],"category_scores_gemma":[0.009311983,0.00054684095,0.0004881104,0.0053001526,0.00027774164,0.0029065732,0.0014464512,0.0029997474,0.029078878],"study_design_candidate":"not_applicable","study_design_consensus":"not_applicable","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00052219396,0.00009019179,0.000472573,0.00047937443,0.00004307829,0.00044637188,0.00005208314,0.00034616276,0.010962379,0.009683538,0.8221077,0.15479442],"study_design_scores_gemma":[0.00023879927,0.00004620954,0.0011814912,0.00014181025,0.00006371342,0.0011850932,0.00004215459,0.0024394393,0.005185576,0.0116288215,0.9778066,0.000040213068],"about_ca_topic_score_codex":0.001021402,"about_ca_topic_score_gemma":0.0016035571,"teacher_disagreement_score":0.033831142,"about_ca_system_score_codex":0.00074187666,"about_ca_system_score_gemma":0.0015060948,"threshold_uncertainty_score":0.113176465},"labels":[],"label_agreement":null},{"id":"W2047019441","doi":"10.1038/ng.2948","title":"De novo CCND2 mutations leading to stabilization of cyclin D2 cause megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome","year":2014,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Microtubule and mitosis dynamics","field":"Biochemistry, Genetics and Molecular Biology","cited_by":151,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of British Columbia; Children's Hospital of Eastern Ontario; University of Ottawa; McGill University and Génome Québec Innovation Centre","funders":"National Institute of Neurological Disorders and Stroke; Medical Research Council; Canadian Institutes of Health Research","keywords":"Cyclin D2; Megalencephaly; Biology; AKT3; Cancer research; Protein kinase B; PI3K/AKT/mTOR pathway; PTEN; GSK-3; Polymicrogyria; Molecular biology; Genetics; Cell cycle; Phosphorylation; Cyclin D1; Signal transduction; AKT1; Neuroscience; Gene","score_opus":0.0060927700395271515,"score_gpt":0.2637567344944351,"score_spread":0.25766396445490797,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2047019441","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9950919,0.0004354296,0.0020255584,0.00029214923,0.00010070213,0.000026682543,0.0003466912,0.000112266796,0.0015685334],"genre_scores_gemma":[0.99847394,0.00011867701,0.0007526865,0.000041125146,0.000031544765,0.00000947404,0.00009875162,0.000023147813,0.00045058894],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99983025,0.000020749316,0.000030840125,0.00004080641,0.000057351597,0.000019953148],"domain_scores_gemma":[0.9996056,0.0001421345,0.00011523099,0.00002770731,0.000018860215,0.00009057195],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.000094217925,0.0008864052,0.0002878985,0.00062791747,0.00040989553,0.000309929,0.00036317957,0.0011145232,0.0015185956],"category_scores_gemma":[0.0006146869,0.00028703082,0.00027695444,0.00040795212,0.00058112293,0.00019783454,0.0004486621,0.0006167923,0.0003222552],"study_design_candidate":"bench_or_experimental","study_design_consensus":"bench_or_experimental","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.000472467,0.00010083281,0.011561063,0.00012001963,0.00010861633,0.20318064,0.0002082215,0.0016378062,0.773621,0.0019870112,0.0010137551,0.0059885983],"study_design_scores_gemma":[0.00040681937,0.000318961,0.09957267,0.00003918088,0.00022503453,0.34206018,0.00025114376,0.009087779,0.5348563,0.0019590384,0.01112347,0.000099483],"about_ca_topic_score_codex":0.00093682803,"about_ca_topic_score_gemma":0.0016103412,"teacher_disagreement_score":0.0015185956,"about_ca_system_score_codex":0.00045909078,"about_ca_system_score_gemma":0.00031313064,"threshold_uncertainty_score":0.005080223},"labels":[],"label_agreement":null},{"id":"W2047498240","doi":"10.1038/ng862","title":"Mutations in the human ortholog of Aristaless cause X-linked mental retardation and epilepsy","year":2002,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Genetics and Neurodevelopmental Disorders","field":"Biochemistry, Genetics and Molecular Biology","cited_by":432,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Children's & Women's Health Centre of British Columbia; University of British Columbia","funders":"","keywords":"Missense mutation; Epilepsy; Homeobox; Biology; Genetics; Mutation; West Syndrome; Gene; Myoclonic epilepsy; Neuroscience","score_opus":0.01465193966091577,"score_gpt":0.2660983745518412,"score_spread":0.25144643489092544,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2047498240","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99188375,0.00091749243,0.00390973,0.00021365065,0.00007404278,0.000013102999,0.00036356057,0.00022252879,0.00240225],"genre_scores_gemma":[0.99572384,0.00033671406,0.0013608235,0.000054481807,0.000020435938,0.000004742433,0.00026947324,0.000027677896,0.0022017953],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9998721,0.00001675022,0.000013202356,0.000022020058,0.000057299818,0.000018548302],"domain_scores_gemma":[0.99974567,0.000067399145,0.00007551219,0.000026249947,0.00001717021,0.000067958994],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00013777635,0.0006294838,0.00036815504,0.0007335543,0.00049575896,0.0003257093,0.00026944242,0.00062443543,0.002175134],"category_scores_gemma":[0.00040551464,0.0001955859,0.00023258035,0.0003957483,0.0006493404,0.00019008409,0.00053833623,0.00041393572,0.0007942307],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0015187858,0.00010431371,0.010238239,0.00019397584,0.00018590255,0.030027848,0.0002835054,0.0012128216,0.92977494,0.004431494,0.0014322121,0.02059599],"study_design_scores_gemma":[0.0005275264,0.00046780886,0.20808451,0.00008856789,0.00047274717,0.10364033,0.0011646488,0.0065209433,0.62141186,0.009424407,0.048024297,0.00017231682],"about_ca_topic_score_codex":0.0013319079,"about_ca_topic_score_gemma":0.0024618146,"teacher_disagreement_score":0.002175134,"about_ca_system_score_codex":0.0002632368,"about_ca_system_score_gemma":0.00029949038,"threshold_uncertainty_score":0.007276535},"labels":[],"label_agreement":null},{"id":"W2049352641","doi":"10.1038/ng0501-87","title":"A susceptibility locus for asthma-related traits on chromosome 7 revealed by genome-wide scan in a founder population","year":2001,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Genetic Associations and Epidemiology","field":"Biochemistry, Genetics and Molecular Biology","cited_by":208,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"McGill University; Montreal General Hospital","funders":"","keywords":"Biology; Genetics; Locus (genetics); Chromosome; Genome Scan; Genome; Population; Gene; Microsatellite; Allele; Demography","score_opus":0.008357324779542399,"score_gpt":0.2697224158572922,"score_spread":0.2613650910777498,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2049352641","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99921644,0.000103946644,0.0002629104,0.000055466608,0.000008895221,0.0000061026103,0.00011868465,0.000010210732,0.00021722684],"genre_scores_gemma":[0.9989491,0.00009524158,0.00037651754,0.000047013757,0.000025215939,0.0000066689795,0.0001684146,0.000009636082,0.0003221075],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9991392,0.00018612458,0.00006521293,0.00035493448,0.00013223066,0.00012219197],"domain_scores_gemma":[0.9991322,0.00035177497,0.0001538316,0.00009193696,0.00009807625,0.0001721533],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00073297153,0.00065680494,0.00072406844,0.0017291445,0.0009920644,0.00053716043,0.0009325747,0.0009010204,0.0024739443],"category_scores_gemma":[0.00156338,0.00032469115,0.0008395211,0.0012006857,0.0007115344,0.00025178335,0.00050091784,0.0009942221,0.00020943792],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.003703675,0.0005864691,0.7358382,0.00007702887,0.0011168269,0.012554907,0.0021239724,0.00032237486,0.22887771,0.00083354505,0.0007400708,0.013225344],"study_design_scores_gemma":[0.00019510394,0.00065456145,0.9813673,0.000020782822,0.0009758105,0.010572537,0.0005571848,0.00094809086,0.0036205573,0.0004058447,0.000649493,0.00003268724],"about_ca_topic_score_codex":0.0059880507,"about_ca_topic_score_gemma":0.0040674848,"teacher_disagreement_score":0.0059880507,"about_ca_system_score_codex":0.00021302947,"about_ca_system_score_gemma":0.00040028468,"threshold_uncertainty_score":0.011906385},"labels":[],"label_agreement":null},{"id":"W2049876198","doi":"10.1038/ng1684","title":"Oral-facial-digital type I protein is required for primary cilia formation and left-right axis specification","year":2005,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Genetic and Kidney Cyst Diseases","field":"Biochemistry, Genetics and Molecular Biology","cited_by":347,"is_retracted":false,"has_abstract":false,"route_ca_aff":false,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"","funders":"Institute of Genetics; Centre National de la Recherche Scientifique","keywords":"Biology; Cilium; Primary (astronomy); Cell biology; Genetics; Anatomy; Physics; Astrophysics","score_opus":0.00819678084987833,"score_gpt":0.24391553892859577,"score_spread":0.23571875807871745,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2049876198","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.98101586,0.0016414748,0.0076657934,0.0004502149,0.00023720066,0.00004755795,0.0017146239,0.00039246652,0.0068347477],"genre_scores_gemma":[0.9909662,0.00024755267,0.0025190555,0.00010849723,0.000016443804,0.00001857061,0.0010662193,0.00015669396,0.0049006697],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99964285,0.000027163063,0.00003358669,0.000083309824,0.00012381891,0.000089242385],"domain_scores_gemma":[0.9994647,0.000065428576,0.00020565142,0.000064390726,0.00003067172,0.00016920053],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0001805468,0.0005076946,0.0003809905,0.0004677911,0.000599156,0.00091638224,0.00066651934,0.00075637415,0.003701259],"category_scores_gemma":[0.0003867926,0.0005303697,0.00043988466,0.00016754137,0.00078389165,0.00035868978,0.00068736885,0.0012104466,0.0017326708],"study_design_candidate":"bench_or_experimental","study_design_consensus":"bench_or_experimental","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00018272456,0.000015087664,0.0005496858,0.000029047778,0.000007792058,0.00047436907,0.0000123747495,0.00008713972,0.99710315,0.00040406364,0.00014890962,0.0009857073],"study_design_scores_gemma":[0.000045880683,0.00004308127,0.017201247,0.000012166031,0.000031188585,0.0015943156,0.000071331415,0.0021913003,0.9738096,0.0002219033,0.004763714,0.000014370183],"about_ca_topic_score_codex":0.0034128246,"about_ca_topic_score_gemma":0.00627878,"teacher_disagreement_score":0.003701259,"about_ca_system_score_codex":0.001101206,"about_ca_system_score_gemma":0.0008428813,"threshold_uncertainty_score":0.012381971},"labels":[],"label_agreement":null},{"id":"W2050252182","doi":"10.1038/ng.631","title":"Variants at IRF5-TNPO3, 17q12-21 and MMEL1 are associated with primary biliary cirrhosis","year":2010,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Liver Diseases and Immunity","field":"Medicine","cited_by":217,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Hôpital Saint-Luc; University of Calgary; Lunenfeld-Tanenbaum Research Institute; Mount Sinai Hospital; Université de Montréal; University of Alberta; Toronto Western Hospital; University of Toronto","funders":"National Institute of Diabetes and Digestive and Kidney Diseases; Canadian Institutes of Health Research; Canada Research Chairs; University Health Network; American Gastroenterological Association","keywords":"Primary biliary cirrhosis; Biology; Genome-wide association study; IRF5; Genetic association; Genetics; Cirrhosis; Single-nucleotide polymorphism; Gene; Internal medicine; Immunology; Genotype; Medicine; Transcription factor","score_opus":0.006444183592760626,"score_gpt":0.2251689921311321,"score_spread":0.21872480853837145,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2050252182","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9978676,0.00035937343,0.00033465182,0.00024032062,0.000035425255,0.0000084045805,0.00028456596,0.000024971534,0.00084470364],"genre_scores_gemma":[0.9988348,0.00007117256,0.0003018317,0.00005243698,0.00003925274,0.0000061676683,0.00013891747,0.000012607578,0.0005427665],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9994854,0.00015831875,0.000059962447,0.000109922825,0.00008321484,0.000103308834],"domain_scores_gemma":[0.99842715,0.0005725703,0.00063070824,0.000079503065,0.00005991233,0.00023017767],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00042446767,0.0010038667,0.0005485621,0.0016697334,0.0006713783,0.0004952489,0.0007066487,0.0014882123,0.007136759],"category_scores_gemma":[0.0020660432,0.00039274184,0.00066641043,0.0014484313,0.0005553365,0.00029847363,0.00038998085,0.0007710904,0.00068037957],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.010067222,0.00043725598,0.80830103,0.0002130497,0.0010118829,0.04142936,0.00074263784,0.0011227462,0.11413661,0.0012904687,0.0023008734,0.018946849],"study_design_scores_gemma":[0.00029586774,0.00045450503,0.9330177,0.00006547142,0.00064927014,0.050940983,0.00037699923,0.0017669807,0.008745422,0.0013080393,0.0023233294,0.000055384888],"about_ca_topic_score_codex":0.0018484402,"about_ca_topic_score_gemma":0.0021030598,"teacher_disagreement_score":0.007136759,"about_ca_system_score_codex":0.00024071813,"about_ca_system_score_gemma":0.00021925528,"threshold_uncertainty_score":0.02387482},"labels":[],"label_agreement":null},{"id":"W2050252352","doi":"10.1038/ng.859","title":"Identification of common variants influencing risk of the tauopathy progressive supranuclear palsy","year":2011,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Neurological diseases and metabolism","field":"Neuroscience","cited_by":632,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of British Columbia","funders":"National Human Genome Research Institute; National Institute on Aging; National Institute of Neurological Disorders and Stroke; National Institute of General Medical Sciences; National Institute of Mental Health; Medical Research Council; National Institutes of Health; Wellcome Trust; CurePSP; Howard Hughes Medical Institute","keywords":"Progressive supranuclear palsy; Tauopathy; Neuropathology; Biology; Genome-wide association study; Tau protein; Single-nucleotide polymorphism; Genetics; Neuroscience; Alzheimer's disease; Disease; Pathology; Neurodegeneration; Genotype; Atrophy; Gene; Medicine","score_opus":0.0190473432319792,"score_gpt":0.2617623983256848,"score_spread":0.2427150550937056,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2050252352","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99639446,0.00054477755,0.0015857341,0.00011479085,0.000029978528,0.000017963212,0.00038231374,0.000036357487,0.0008937069],"genre_scores_gemma":[0.9987929,0.000122225,0.0006115588,0.000037843864,0.000023506442,0.000005234442,0.00016377395,0.000017495648,0.00022546554],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99877745,0.00029241305,0.00020134298,0.0003725851,0.00021865664,0.00013763568],"domain_scores_gemma":[0.9979513,0.001021293,0.0005305598,0.00014886697,0.0001464137,0.00020154552],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0006718315,0.0012089158,0.0008514435,0.0023421561,0.0007775786,0.0008478485,0.0007432664,0.0015598692,0.003545836],"category_scores_gemma":[0.0027228494,0.00039966052,0.0010592343,0.0018740365,0.0005680315,0.00030034134,0.00059131114,0.00083022023,0.00035242247],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.008625196,0.00047485475,0.58304155,0.00032559593,0.0045166514,0.036936637,0.0015794984,0.004847594,0.3026987,0.0034429247,0.0014671847,0.052043512],"study_design_scores_gemma":[0.00047005236,0.00093347934,0.94176227,0.00013064439,0.0028940064,0.022536572,0.00047285296,0.005986233,0.01976443,0.0028032062,0.0021227815,0.00012346852],"about_ca_topic_score_codex":0.004225255,"about_ca_topic_score_gemma":0.0045931204,"teacher_disagreement_score":0.004225255,"about_ca_system_score_codex":0.00028089626,"about_ca_system_score_gemma":0.00034741286,"threshold_uncertainty_score":0.01186204},"labels":[],"label_agreement":null},{"id":"W2050729907","doi":"10.1038/ng.390","title":"Mutation in TACO1, encoding a translational activator of COX I, results in cytochrome c oxidase deficiency and late-onset Leigh syndrome","year":2009,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Mitochondrial Function and Pathology","field":"Biochemistry, Genetics and Molecular Biology","cited_by":309,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"McGill University Health Centre; McGill University; Montreal Neurological Institute and Hospital; McGill Genome Centre","funders":"","keywords":"Biology; Cytochrome c oxidase; Genetics; Mitochondrial DNA; Complementation; Translation (biology); Mitochondrion; Gene; Saccharomyces cerevisiae; Molecular biology; Mutant; Messenger RNA","score_opus":0.008432779676854407,"score_gpt":0.2583167782955692,"score_spread":0.2498839986187148,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2050729907","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9953375,0.0003488201,0.002113517,0.0003856501,0.000111176385,0.000032666354,0.00024373477,0.00014952217,0.0012773365],"genre_scores_gemma":[0.9980202,0.00010255805,0.0007829071,0.000071248716,0.000052557865,0.000010467526,0.00012078761,0.000043316697,0.00079589355],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99971765,0.00005265594,0.00003951748,0.00005793684,0.00009181169,0.000040384417],"domain_scores_gemma":[0.9987092,0.00057125674,0.00031133628,0.000044337397,0.000039566417,0.00032438381],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00023163849,0.0014325824,0.00052505505,0.0012307727,0.00062986725,0.00041377993,0.0006114982,0.0015401382,0.0013347205],"category_scores_gemma":[0.0013208135,0.00040377284,0.00058745145,0.00068009406,0.0010176076,0.00030065706,0.00041308688,0.00088790135,0.00044874122],"study_design_candidate":"bench_or_experimental","study_design_consensus":"bench_or_experimental","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0028041792,0.00052080234,0.02020485,0.00014691825,0.00019652261,0.45648456,0.0008495774,0.0013450007,0.5043895,0.0017803763,0.0015354685,0.009742227],"study_design_scores_gemma":[0.0007683537,0.0013885121,0.11220492,0.000098713346,0.0005518165,0.6572919,0.00049618416,0.00982388,0.21108522,0.0014711521,0.004617539,0.00020184107],"about_ca_topic_score_codex":0.0015880021,"about_ca_topic_score_gemma":0.0014592,"teacher_disagreement_score":0.0015880021,"about_ca_system_score_codex":0.0006236257,"about_ca_system_score_gemma":0.000312812,"threshold_uncertainty_score":0.0045247674},"labels":[],"label_agreement":null},{"id":"W2050863429","doi":"10.1038/ng1448","title":"Lifespan and mitochondrial control of neurodegeneration","year":2004,"lang":"en","type":"review","venue":"Nature Genetics","topic":"Mitochondrial Function and Pathology","field":"Biochemistry, Genetics and Molecular Biology","cited_by":108,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"SickKids Foundation; Hospital for Sick Children; University of Toronto","funders":"National Institutes of Health; Macula Vision Research Foundation","keywords":"Neurodegeneration; Biology; Mitochondrion; Programmed cell death; Cell biology; Neuroscience; Genetics; Apoptosis","score_opus":0.01223782949713774,"score_gpt":0.282928931284739,"score_spread":0.27069110178760125,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2050863429","genre_codex":"review","genre_gemma":"review","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"review","genre_consensus":"review","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.00014589752,0.99604565,0.00061530806,0.00072384044,0.00086464593,0.000004474831,0.000019008661,0.000019746061,0.0015614635],"genre_scores_gemma":[0.0010632295,0.99557036,0.0006026872,0.0003901078,0.0006649397,0.000009936631,0.0000331624,0.000003028444,0.0016625364],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.99984324,0.000022882432,0.000023980858,0.00003116427,0.00006108422,0.000017677148],"domain_scores_gemma":[0.9996718,0.0001272488,0.000039491144,0.000016191792,0.00010062139,0.000044754663],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0008978084,0.0013065764,0.0017622908,0.0014588118,0.00040922363,0.0013241513,0.0016949631,0.002140126,0.0025652484],"category_scores_gemma":[0.0007201645,0.0003534637,0.00032337452,0.0019359206,0.0011685631,0.0019259463,0.00083491084,0.0024741078,0.0022089866],"study_design_candidate":"not_applicable","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00020393013,0.00006734209,0.00027858003,0.0061245393,0.000093210154,0.0005978569,0.0000662768,0.00082302676,0.0049395645,0.010600142,0.071857475,0.9043481],"study_design_scores_gemma":[0.000029994802,0.000044048105,0.0007052007,0.0010038214,0.0000705246,0.0011714341,0.00007066875,0.00013012582,0.0009216978,0.0069733756,0.9888593,0.000019853014],"about_ca_topic_score_codex":0.0012493719,"about_ca_topic_score_gemma":0.0031795169,"teacher_disagreement_score":0.0025652484,"about_ca_system_score_codex":0.0010959327,"about_ca_system_score_gemma":0.00088359794,"threshold_uncertainty_score":0.008581579},"labels":[],"label_agreement":null},{"id":"W2051582141","doi":"10.1038/ng.945","title":"Mutations in TRPV4 cause an inherited arthropathy of hands and feet","year":2011,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Ion Channels and Receptors","field":"Neuroscience","cited_by":156,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Alberta","funders":"National Health and Medical Research Council; National Medical Research Council; State Government of Victoria; Australian Government","keywords":"TRPV4; Spinal osteoarthropathy; Biology; Mutant; Phenotype; Mutation; Genetics; Transient receptor potential channel; Cell biology; Gene; Receptor","score_opus":0.04747555700970352,"score_gpt":0.2896683010499977,"score_spread":0.24219274404029417,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2051582141","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.98375297,0.0012894925,0.0049986136,0.0014120153,0.00040288188,0.00007675442,0.0007897129,0.00035907,0.006918612],"genre_scores_gemma":[0.9948067,0.0002746919,0.0020953487,0.00022375229,0.00012985207,0.000014020773,0.00013610262,0.00007266854,0.0022469552],"study_design_codex":"case_report","study_design_gemma":"observational","domain_scores_codex":[0.99918586,0.00009820468,0.000100694364,0.00019364659,0.00028850808,0.000133142],"domain_scores_gemma":[0.9989837,0.0004311877,0.00024163428,0.000044452816,0.000074105585,0.00022494797],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00033329404,0.0028906872,0.0007700022,0.0014328901,0.000980111,0.0006398478,0.0010166285,0.0030555497,0.005056017],"category_scores_gemma":[0.0017070473,0.0005642075,0.0010974439,0.00081949116,0.0014859636,0.00049026305,0.0011705128,0.0014087302,0.00061467255],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0010756755,0.00021790489,0.011917056,0.00025069676,0.00034506692,0.6372514,0.00053590006,0.001538872,0.3275399,0.0027727208,0.002255192,0.014299618],"study_design_scores_gemma":[0.0005265232,0.00080343464,0.081666924,0.00017170869,0.0005772283,0.83063716,0.00065394567,0.0050058844,0.070074044,0.003730406,0.0059288326,0.0002238852],"about_ca_topic_score_codex":0.0023622676,"about_ca_topic_score_gemma":0.002898416,"teacher_disagreement_score":0.005056017,"about_ca_system_score_codex":0.00075481733,"about_ca_system_score_gemma":0.0006037108,"threshold_uncertainty_score":0.01691407},"labels":[],"label_agreement":null},{"id":"W2051870471","doi":"10.1038/ng.2941","title":"Rare missense variants in POT1 predispose to familial cutaneous malignant melanoma","year":2014,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Telomeres, Telomerase, and Senescence","field":"Medicine","cited_by":333,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"McGill University and Génome Québec Innovation Centre","funders":"National Cancer Institute; National Institutes of Health","keywords":"CDKN2A; Biology; Genetics; Missense mutation; Telomere; Shelterin; Exome sequencing; Exome; Melanoma; Gene; Mutation","score_opus":0.007753586984513472,"score_gpt":0.24994965717347278,"score_spread":0.2421960701889593,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2051870471","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99262506,0.0008774085,0.0016156838,0.00039448132,0.00014198625,0.000034606364,0.00031784052,0.00018165099,0.003811305],"genre_scores_gemma":[0.9987735,0.00009731927,0.00035510684,0.000055935398,0.00008013194,0.0000050866147,0.00006114585,0.000018727294,0.0005530965],"study_design_codex":"case_report","study_design_gemma":"observational","domain_scores_codex":[0.999532,0.0000783698,0.00005899696,0.00013519048,0.00012622739,0.00006930319],"domain_scores_gemma":[0.99831665,0.00073454826,0.00050816365,0.00010264743,0.000088323795,0.00024967184],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00040464386,0.0017148016,0.00062031794,0.0019127021,0.0008846131,0.0007332688,0.0006550234,0.00252709,0.007168444],"category_scores_gemma":[0.0028129646,0.00043307358,0.0007549195,0.0010534428,0.0006820198,0.00041958867,0.0006203824,0.0010460763,0.00078751997],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0019503931,0.00028010804,0.13793497,0.00027841236,0.0005389896,0.70672566,0.001470912,0.0015734597,0.12971346,0.0022640885,0.0024789432,0.014790579],"study_design_scores_gemma":[0.0001861989,0.00047165345,0.239414,0.00017302002,0.00056223234,0.7376228,0.00051182904,0.003014766,0.011642744,0.0024446703,0.0038552785,0.000100759644],"about_ca_topic_score_codex":0.0005982504,"about_ca_topic_score_gemma":0.00072344043,"teacher_disagreement_score":0.007168444,"about_ca_system_score_codex":0.00030234957,"about_ca_system_score_gemma":0.00017658023,"threshold_uncertainty_score":0.023980856},"labels":[],"label_agreement":null},{"id":"W2051959338","doi":"10.1038/ng1905","title":"Loss of DMP1 causes rickets and osteomalacia and identifies a role for osteocytes in mineral metabolism","year":2006,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Parathyroid Disorders and Treatments","field":"Medicine","cited_by":1198,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Shriners Hospitals for Children - Canada; McGill University; Children's Hospital of Eastern Ontario","funders":"National Institute of Dental and Craniofacial Research; National Institute of Arthritis and Musculoskeletal and Skin Diseases; National Institute of Diabetes and Digestive and Kidney Diseases","keywords":"DMP1; PHEX; Hypophosphatemic Rickets; Osteocyte; Rickets; Fibroblast growth factor 23; Osteomalacia; Hypophosphatemia; Biology; Endocrinology; Bone remodeling; Internal medicine; Osteoblast; Osteosclerosis; Osteoclast; Genetics; Pathology; Gene; Medicine; Calcium; Vitamin D and neurology; Parathyroid hormone","score_opus":0.0060800206153547335,"score_gpt":0.26488210967315684,"score_spread":0.2588020890578021,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2051959338","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9821216,0.005145173,0.008019523,0.00078510126,0.000093859126,0.000027786251,0.0010828979,0.00016112803,0.002562871],"genre_scores_gemma":[0.99261355,0.001479779,0.0034349074,0.00013099448,0.000030981384,0.000026312398,0.00053600996,0.00004540365,0.0017020614],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.99979454,0.000025359988,0.00002036017,0.000050616014,0.00007805364,0.000031082433],"domain_scores_gemma":[0.9997043,0.000104363215,0.00008509499,0.000028108327,0.000019757525,0.000058375987],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00019749285,0.00062345486,0.0004704832,0.0011556316,0.00025676689,0.00044641792,0.0005190426,0.0008254286,0.0022527142],"category_scores_gemma":[0.0005238568,0.00042944666,0.00032230804,0.00047844823,0.0006804149,0.00029191838,0.000612674,0.0009473794,0.0004167781],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0008323751,0.000035729267,0.008704884,0.00010331441,0.0000560092,0.0064087436,0.000055278808,0.00033707914,0.9729671,0.0010294485,0.0004633455,0.00900675],"study_design_scores_gemma":[0.00015761526,0.0002485927,0.08304953,0.000030781222,0.00014715867,0.055545524,0.00020308846,0.0023085917,0.8448575,0.0017533309,0.01166407,0.000034214747],"about_ca_topic_score_codex":0.0005908641,"about_ca_topic_score_gemma":0.00053561456,"teacher_disagreement_score":0.0022527142,"about_ca_system_score_codex":0.00029290025,"about_ca_system_score_gemma":0.0002084754,"threshold_uncertainty_score":0.0075361133},"labels":[],"label_agreement":null},{"id":"W2052404098","doi":"10.1038/ng0403-439","title":"Wanted: regulatory SNPs","year":2003,"lang":"en","type":"letter","venue":"Nature Genetics","topic":"Genetic Associations and Epidemiology","field":"Biochemistry, Genetics and Molecular Biology","cited_by":110,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"McGill University and Génome Québec Innovation Centre","funders":"","keywords":"Biology; Single-nucleotide polymorphism; Genetics; Computational biology; Functional genomics; Gene; Identification (biology); Genomics; Genome; Genotype","score_opus":0.007638027393345542,"score_gpt":0.2517482428054301,"score_spread":0.24411021541208458,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2052404098","genre_codex":"commentary","genre_gemma":"editorial","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"editorial","genre_consensus":null,"domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.0006871013,0.0022193466,0.0008849808,0.92720664,0.05784361,0.00002805819,0.00016904801,0.00018120058,0.010780054],"genre_scores_gemma":[0.0050445376,0.0007026802,0.0005421799,0.91149914,0.05047348,0.00005696127,0.000093225884,0.000052390627,0.031535447],"study_design_codex":"not_applicable","study_design_gemma":"not_applicable","domain_scores_codex":[0.9979528,0.000528743,0.00017913553,0.00046938768,0.00050731184,0.00036257427],"domain_scores_gemma":[0.9918058,0.004937057,0.000263476,0.0005491848,0.00083200814,0.00161252],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0034568417,0.0011710301,0.0018070972,0.00075844955,0.004390283,0.0036184401,0.0015886554,0.04051872,0.020777624],"category_scores_gemma":[0.018922659,0.0007572435,0.0013351407,0.00048630268,0.0031030169,0.00270777,0.0018492682,0.036153648,0.014943175],"study_design_candidate":"not_applicable","study_design_consensus":"not_applicable","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00008071419,0.00002453008,0.0005377609,0.000027692768,0.000022544375,0.0013784381,0.00007169092,0.000041420673,0.00036505505,0.0061812196,0.9773566,0.013912208],"study_design_scores_gemma":[0.00042653154,0.00010513991,0.0028691944,0.00023653771,0.00008378248,0.0044346345,0.00033665885,0.00054159027,0.00078573124,0.054263953,0.9358226,0.00009361169],"about_ca_topic_score_codex":0.0026234963,"about_ca_topic_score_gemma":0.0062947264,"teacher_disagreement_score":0.04051872,"about_ca_system_score_codex":0.002174637,"about_ca_system_score_gemma":0.0014708212,"threshold_uncertainty_score":0.069508016},"labels":[],"label_agreement":null},{"id":"W2053002029","doi":"10.1038/ng.372","title":"Narcolepsy is strongly associated with the T-cell receptor alpha locus","year":2009,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Sleep and Wakefulness Research","field":"Neuroscience","cited_by":481,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Université de Montréal","funders":"National Heart, Lung, and Blood Institute; National Institute of Allergy and Infectious Diseases; Canadian Institutes of Health Research; National Institute of Neurological Disorders and Stroke; National Institute of Mental Health; Howard Hughes Medical Institute","keywords":"Narcolepsy; Cataplexy; Biology; Human leukocyte antigen; Allele; Locus (genetics); Genetics; Odds ratio; Genotype; Genome-wide association study; T-cell receptor; Immunology; Single-nucleotide polymorphism; Internal medicine; T cell; Neuroscience; Medicine; Gene; Immune system; Antigen","score_opus":0.016908462353333313,"score_gpt":0.2775904986055521,"score_spread":0.2606820362522188,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2053002029","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9958061,0.00051582645,0.0012688935,0.000270935,0.000075275406,0.000017070788,0.00036054885,0.000058906102,0.0016264172],"genre_scores_gemma":[0.9979394,0.00019713478,0.00049531605,0.0000818848,0.00008531309,0.000010186855,0.00024379326,0.000043521755,0.0009034306],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.999199,0.00027233973,0.00007916157,0.00022323105,0.00013657623,0.00008961604],"domain_scores_gemma":[0.99789244,0.00064959825,0.00088809617,0.00015251081,0.00009493465,0.0003224521],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00032770424,0.0012539524,0.00064138154,0.0017622262,0.0008809432,0.0005264891,0.00052765216,0.0012585818,0.0051173354],"category_scores_gemma":[0.0010374552,0.0004997727,0.00084588316,0.00090389664,0.0008036485,0.00023267641,0.000642252,0.0011939962,0.0007321572],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0046288213,0.00016370806,0.083595715,0.00009581134,0.00063566345,0.014159945,0.00055063784,0.0005047887,0.888727,0.0007374507,0.00075614214,0.0054443404],"study_design_scores_gemma":[0.0002741378,0.0006901426,0.9367024,0.00010490766,0.0006203727,0.029529564,0.00044432437,0.0017962278,0.026184833,0.0010369648,0.0025255615,0.000090605085],"about_ca_topic_score_codex":0.002225296,"about_ca_topic_score_gemma":0.002108952,"teacher_disagreement_score":0.0051173354,"about_ca_system_score_codex":0.00032755308,"about_ca_system_score_gemma":0.00025477944,"threshold_uncertainty_score":0.01711917},"labels":[],"label_agreement":null},{"id":"W2053235668","doi":"10.1038/ng1327","title":"A previously unidentified MECP2 open reading frame defines a new protein isoform relevant to Rett syndrome","year":2004,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Genetics and Neurodevelopmental Disorders","field":"Biochemistry, Genetics and Molecular Biology","cited_by":346,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Centre for Addiction and Mental Health; Victoria General Hospital; University of Toronto; Hospital for Sick Children","funders":"Canadian Institutes of Health Research","keywords":"Rett syndrome; MECP2; Biology; Gene isoform; Open reading frame; Genetics; Mutation; Gene; Peptide sequence; Phenotype","score_opus":0.009936155156947749,"score_gpt":0.259332060004432,"score_spread":0.24939590484748425,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2053235668","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99403024,0.0007765079,0.0026410988,0.00027202923,0.00017800175,0.00003289663,0.00040773346,0.00007927547,0.0015822507],"genre_scores_gemma":[0.99322927,0.0005121775,0.003488749,0.00014515445,0.00018131317,0.000030615774,0.0009718791,0.000057209145,0.0013835924],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99982494,0.000011714171,0.000028292565,0.000057462432,0.00003803236,0.000039681814],"domain_scores_gemma":[0.99955434,0.00012056004,0.00012697178,0.000034723736,0.000051258397,0.00011207571],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00016813878,0.00078358134,0.00039597304,0.00086191477,0.000494307,0.0006084762,0.0006074813,0.000986448,0.0013884102],"category_scores_gemma":[0.00059431675,0.00023556284,0.00058024266,0.0003894858,0.00074901985,0.00041636408,0.00042050125,0.0009442416,0.0007370358],"study_design_candidate":"bench_or_experimental","study_design_consensus":"bench_or_experimental","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0005744585,0.00009125734,0.0032286895,0.000058084413,0.000025598378,0.029449116,0.00013961099,0.00013559245,0.9615579,0.0011974594,0.00028444052,0.003257872],"study_design_scores_gemma":[0.00025906216,0.00090020965,0.11086776,0.000053033036,0.0002913327,0.15821297,0.0005968548,0.0027557584,0.70546615,0.0031316571,0.01734662,0.00011859214],"about_ca_topic_score_codex":0.0008944941,"about_ca_topic_score_gemma":0.00087396754,"teacher_disagreement_score":0.0013884102,"about_ca_system_score_codex":0.00056051894,"about_ca_system_score_gemma":0.00031895872,"threshold_uncertainty_score":0.004644692},"labels":[],"label_agreement":null},{"id":"W2053450368","doi":"10.1038/ng1751","title":"Distribution of fitness effects among beneficial mutations before selection in experimental populations of bacteria","year":2006,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Evolution and Genetic Dynamics","field":"Biochemistry, Genetics and Molecular Biology","cited_by":275,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Wilfrid Laurier University; University of Ottawa","funders":"","keywords":"Biology; Selection (genetic algorithm); Evolutionary biology; Population; Genetics; Genetic Fitness; Mutation; Pseudomonas fluorescens; Experimental evolution; Fitness landscape; Gene; Bacteria; Demography","score_opus":0.0031840443954119922,"score_gpt":0.25372075308124475,"score_spread":0.2505367086858328,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2053450368","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9995815,0.00004088447,0.0002504337,0.0000068630375,0.0000012291905,0.0000012192575,0.000015411675,0.0000036056567,0.000098944256],"genre_scores_gemma":[0.9993327,0.000031766853,0.00035078684,0.000012784796,0.0000025376173,0.000006694306,0.00006643379,0.000009651096,0.00018666802],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9995333,0.000138572,0.000034427172,0.00013968468,0.00008371826,0.00007026447],"domain_scores_gemma":[0.9941116,0.0042455215,0.00042342467,0.00048240612,0.000408557,0.0003283931],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0007411434,0.00016109571,0.0003722647,0.0007338029,0.00043263048,0.00058140885,0.0005527402,0.00059040985,0.0012685172],"category_scores_gemma":[0.0029756255,0.0003443461,0.00019758193,0.00029267804,0.00085272186,0.00046843925,0.0004152283,0.00077255367,0.00014170737],"study_design_candidate":"bench_or_experimental","study_design_consensus":"bench_or_experimental","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.001544718,0.00031837227,0.0205799,0.00007939588,0.00007389938,0.00009906472,0.00032296244,0.0032715918,0.9652786,0.001614555,0.00007460516,0.0067422716],"study_design_scores_gemma":[0.0003111423,0.002877334,0.418373,0.000039822793,0.00015045844,0.0007591816,0.0010259822,0.04083826,0.5309512,0.0037148888,0.000779041,0.00017970942],"about_ca_topic_score_codex":0.0009199494,"about_ca_topic_score_gemma":0.0010189348,"teacher_disagreement_score":0.0012685172,"about_ca_system_score_codex":0.0007009426,"about_ca_system_score_gemma":0.00020347875,"threshold_uncertainty_score":0.005085647},"labels":[],"label_agreement":null},{"id":"W2053525445","doi":"10.1038/87386","title":"Trinucleotide repeat expansions in familial/sporadic breast/ovarian cancer: searching for novel predisposition genes","year":2001,"lang":"en","type":"article","venue":"Nature Genetics","topic":"RNA modifications and cancer","field":"Biochemistry, Genetics and Molecular Biology","cited_by":0,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Toronto; Lunenfeld-Tanenbaum Research Institute; Mount Sinai Hospital","funders":"","keywords":"Biology; Genetics; Gene; Ovarian cancer; Breast cancer; Cancer","score_opus":0.013000684402453607,"score_gpt":0.29182216970655844,"score_spread":0.27882148530410483,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2053525445","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.997503,0.00085301854,0.00047282703,0.00006488274,0.000010302899,0.000010063426,0.00019445631,0.00001980462,0.00087165984],"genre_scores_gemma":[0.99756336,0.0005181673,0.0010645186,0.00006199033,0.000027325437,0.000008519109,0.00022289135,0.000008853049,0.0005243405],"study_design_codex":"observational","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99990356,0.000018475266,0.000012755042,0.00002749506,0.000022221377,0.00001555873],"domain_scores_gemma":[0.99974436,0.00009823484,0.00007285283,0.000014577096,0.000021488439,0.00004856688],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00019470135,0.00019087213,0.0002541644,0.001682221,0.00030300894,0.00021896677,0.00026298696,0.00039204233,0.0016358529],"category_scores_gemma":[0.00051847246,0.00014161564,0.00016742796,0.0010996682,0.00019967924,0.00008534178,0.00013049041,0.0002333636,0.00027436388],"study_design_candidate":"bench_or_experimental","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.004174626,0.0002856795,0.5873585,0.00032718226,0.00034620863,0.02711751,0.00073274306,0.0011147799,0.32813692,0.001172995,0.0023121696,0.046920672],"study_design_scores_gemma":[0.00016179736,0.00043633283,0.88387424,0.000058892852,0.00071008474,0.06428581,0.00063193747,0.0023907733,0.039796107,0.0014523824,0.0061572157,0.00004441144],"about_ca_topic_score_codex":0.0011580973,"about_ca_topic_score_gemma":0.0018765829,"teacher_disagreement_score":0.001682221,"about_ca_system_score_codex":0.0001466322,"about_ca_system_score_gemma":0.00013626002,"threshold_uncertainty_score":0.0054724813},"labels":[],"label_agreement":null},{"id":"W2053997077","doi":"10.1038/ng.3216","title":"Recombination affects accumulation of damaging and disease-associated mutations in human populations","year":2015,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Evolution and Genetic Dynamics","field":"Biochemistry, Genetics and Molecular Biology","cited_by":95,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Université de Montréal; Centre Hospitalier Universitaire Sainte-Justine","funders":"","keywords":"Biology; Recombination; Genetics; Genome; Gene; Mutation; Gene density; Human genome; Evolutionary biology","score_opus":0.032035844928388145,"score_gpt":0.34887497085660396,"score_spread":0.31683912592821584,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2053997077","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99835616,0.00030345068,0.0005976333,0.000029583709,0.000005690205,0.000004554591,0.00006610792,0.000019990877,0.0006166816],"genre_scores_gemma":[0.99905294,0.00015364288,0.0003117742,0.000021037706,0.000009387949,0.000002546836,0.00009432628,0.000014051016,0.0003403008],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9995492,0.00012529228,0.00004103604,0.00015067628,0.00007387107,0.000059943864],"domain_scores_gemma":[0.9993424,0.00026461465,0.0001547928,0.00008401128,0.000057817633,0.000096478354],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0005271454,0.000257053,0.00030701747,0.0011242144,0.00026233008,0.00052545936,0.00028741884,0.00055164413,0.0022005935],"category_scores_gemma":[0.0010715813,0.0002443686,0.0002766565,0.0005225502,0.00041006066,0.00023369024,0.00038652171,0.0005012897,0.00023782431],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0016472457,0.00016596745,0.07114054,0.00008788025,0.00038085986,0.0013808986,0.00037447008,0.002442273,0.9019968,0.00207572,0.00022828644,0.018079072],"study_design_scores_gemma":[0.00025989374,0.0021553861,0.7451118,0.000043590324,0.0008302367,0.018275447,0.000628665,0.009391414,0.21219741,0.005682248,0.005320226,0.000103643826],"about_ca_topic_score_codex":0.00045173545,"about_ca_topic_score_gemma":0.00039553634,"teacher_disagreement_score":0.0022005935,"about_ca_system_score_codex":0.00016177208,"about_ca_system_score_gemma":0.0001540108,"threshold_uncertainty_score":0.0073617697},"labels":[],"label_agreement":null},{"id":"W2054153086","doi":"10.1038/ng.327","title":"Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants","year":2009,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Genomic variations and chromosomal abnormalities","field":"Biochemistry, Genetics and Molecular Biology","cited_by":1096,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"McGill University; Population Health Research Institute; McMaster University","funders":"Eunice Kennedy Shriver National Institute of Child Health and Human Development; National Center for Research Resources; National Institute of Environmental Health Sciences; National Institute of Diabetes and Digestive and Kidney Diseases; National Heart, Lung, and Blood Institute; Economic and Social Research Council; British Heart Foundation; Wellcome Trust","keywords":"Single-nucleotide polymorphism; Biology; Genetics; Copy-number variation; Locus (genetics); Genome-wide association study; Allele; Myocardial infarction; Genome; Gene; Genotype; Medicine; Internal medicine","score_opus":0.0037262463916524673,"score_gpt":0.20310986020425614,"score_spread":0.19938361381260367,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2054153086","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9986261,0.00040614145,0.00029426612,0.00009079854,0.000013767592,0.0000037473533,0.0002279564,0.000011199016,0.00032596468],"genre_scores_gemma":[0.99927396,0.00010641181,0.00017429273,0.00002060042,0.000026835314,0.0000032972844,0.00016541047,0.0000055923647,0.00022360365],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.999311,0.00025315676,0.00006385216,0.00017193092,0.00010914554,0.000090931375],"domain_scores_gemma":[0.9970497,0.0014934435,0.00071835367,0.00021531811,0.00014043646,0.00038265964],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0009037937,0.00050869153,0.0006351695,0.0014638047,0.00037458917,0.0005916669,0.0007045463,0.0010050539,0.0025654496],"category_scores_gemma":[0.0028429977,0.00031599854,0.0008827854,0.0013111638,0.0004194363,0.00027127485,0.00041722012,0.0010233022,0.0002110329],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0043481174,0.00018223481,0.9516165,0.000057174762,0.0015534422,0.0021305217,0.00018057782,0.00039336696,0.032712206,0.00023109827,0.00030681718,0.006287887],"study_design_scores_gemma":[0.000033240045,0.000100808706,0.9973162,0.000003497346,0.00024980248,0.0010978677,0.000029728233,0.00039331397,0.00058442197,0.000111068766,0.00007281442,0.0000074053005],"about_ca_topic_score_codex":0.0017502701,"about_ca_topic_score_gemma":0.002067365,"teacher_disagreement_score":0.0025654496,"about_ca_system_score_codex":0.00016410329,"about_ca_system_score_gemma":0.0001662051,"threshold_uncertainty_score":0.008582234},"labels":[],"label_agreement":null},{"id":"W2054519090","doi":"10.1038/ng.2900","title":"Recurrent somatic mutations of PTPN1 in primary mediastinal B cell lymphoma and Hodgkin lymphoma","year":2014,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Protein Tyrosine Phosphatases","field":"Biochemistry, Genetics and Molecular Biology","cited_by":195,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of British Columbia; BC Cancer Agency","funders":"","keywords":"Biology; Lymphoma; Missense mutation; Cancer research; T-cell lymphoma; Frameshift mutation; Mutation; Gene; Genetics; Immunology","score_opus":0.004193126112541316,"score_gpt":0.22652530201022475,"score_spread":0.22233217589768342,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2054519090","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99868184,0.000329468,0.00014039107,0.000029433406,0.0000064711576,0.0000033817037,0.00004561923,0.000010965794,0.0007525835],"genre_scores_gemma":[0.9996586,0.00007974579,0.0000738786,0.0000073472793,0.000008822017,0.0000011921076,0.00003234477,0.0000023725438,0.00013576113],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.99981135,0.000018400962,0.000028152332,0.00004039132,0.00006647208,0.000035303863],"domain_scores_gemma":[0.9996557,0.00009320996,0.00010617405,0.000028080813,0.000027998343,0.00008878487],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0002175326,0.00024617676,0.00023327392,0.0008605004,0.00023788172,0.00038660888,0.00028861224,0.0005293997,0.0016197236],"category_scores_gemma":[0.0010857034,0.00021084063,0.0001584495,0.00052155746,0.0004033154,0.00023654143,0.0004130707,0.00023010442,0.0003096649],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0017768607,0.00012316667,0.28541493,0.00018248269,0.0001120248,0.17944688,0.000784952,0.0009182035,0.5063638,0.0006336749,0.0007029976,0.023539983],"study_design_scores_gemma":[0.00010836134,0.00033857158,0.5523168,0.000018808661,0.00020510606,0.39128172,0.00044679156,0.002156725,0.050342154,0.0006507362,0.0021035052,0.000030679606],"about_ca_topic_score_codex":0.0008633347,"about_ca_topic_score_gemma":0.0008904698,"teacher_disagreement_score":0.0016197236,"about_ca_system_score_codex":0.00040619326,"about_ca_system_score_gemma":0.00016108343,"threshold_uncertainty_score":0.005418539},"labels":[],"label_agreement":null},{"id":"W2054789602","doi":"10.1038/ng1073","title":"Nuclear genetic control of mitochondrial DNA segregation","year":2003,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Mitochondrial Function and Pathology","field":"Biochemistry, Genetics and Molecular Biology","cited_by":145,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"McGill University; Montreal Neurological Institute and Hospital","funders":"McGill University","keywords":"Biology; Heteroplasmy; Mitochondrial DNA; Genetics; Nuclear gene; Nuclear DNA; Genome; Gene; Phenotype; Quantitative trait locus; mtDNA control region; Mitochondrion; Genotype; Haplotype","score_opus":0.004900261912405378,"score_gpt":0.22396369123954968,"score_spread":0.2190634293271443,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2054789602","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9519603,0.0026995544,0.030513586,0.0009546221,0.00023735098,0.00002164109,0.00038711485,0.0006357562,0.012589944],"genre_scores_gemma":[0.99567705,0.0003043469,0.0017729787,0.00003843537,0.000016801694,0.000005140835,0.00009539656,0.0000900295,0.001999738],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99968684,0.000050159557,0.00002547598,0.000084988395,0.00010195767,0.00005057539],"domain_scores_gemma":[0.9990189,0.00033853465,0.00022729224,0.00014884256,0.000094878626,0.00017142885],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00028211932,0.00036280186,0.0003215711,0.00051626586,0.0004338461,0.00097353774,0.0006610617,0.0005412055,0.0021847654],"category_scores_gemma":[0.00088655466,0.00027329245,0.00019433875,0.0002735075,0.000986965,0.0006260044,0.00075022277,0.0007807933,0.00071257877],"study_design_candidate":"bench_or_experimental","study_design_consensus":"bench_or_experimental","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00013014891,0.000012141589,0.00037202702,0.000022171074,0.0000031893921,0.00017169208,0.000053616484,0.00020415711,0.9921163,0.003699795,0.0000868749,0.0031280664],"study_design_scores_gemma":[0.00006146918,0.00009832383,0.0095232,0.000017271968,0.000018438961,0.0010605392,0.00014786416,0.0049922033,0.9749321,0.0036175628,0.0054968656,0.00003420939],"about_ca_topic_score_codex":0.0014317606,"about_ca_topic_score_gemma":0.0025522995,"teacher_disagreement_score":0.0021847654,"about_ca_system_score_codex":0.0010602332,"about_ca_system_score_gemma":0.0003253375,"threshold_uncertainty_score":0.0076925755},"labels":[],"label_agreement":null},{"id":"W2055068525","doi":"10.1038/ng.2980","title":"Brain-expressed exons under purifying selection are enriched for de novo mutations in autism spectrum disorder","year":2014,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Genetics and Neurodevelopmental Disorders","field":"Biochemistry, Genetics and Molecular Biology","cited_by":174,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Ontario Genomics; University of Toronto; SickKids Foundation; Toronto Centre for Phenogenomics; Hospital for Sick Children","funders":"Canadian Institutes of Health Research","keywords":"Biology; Missense mutation; Exon; Genetics; Autism spectrum disorder; Autism; Gene; Phenotype; Medicine","score_opus":0.007020948816283127,"score_gpt":0.2508992820463375,"score_spread":0.24387833323005437,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2055068525","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9980627,0.00035860893,0.000614042,0.000050995735,0.000016767395,0.000003926871,0.00025044644,0.00002632825,0.0006162196],"genre_scores_gemma":[0.99829835,0.00013857725,0.00064491126,0.000083797626,0.000012147074,0.000004736189,0.00033066014,0.000027201786,0.00045962984],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.99977976,0.000026401482,0.000025171672,0.000062122315,0.000065598164,0.000041036346],"domain_scores_gemma":[0.9995486,0.00015149836,0.0001369828,0.000031432937,0.000045203466,0.00008621364],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00015058306,0.0002814941,0.00036257211,0.0009425167,0.0003190186,0.0003998118,0.00029143534,0.00046286004,0.0018121989],"category_scores_gemma":[0.00048253292,0.000174752,0.0003368277,0.00042502722,0.0003198799,0.00013890593,0.000303156,0.00040175323,0.0004060486],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0007148528,0.00004876161,0.047343463,0.00007612959,0.00021078829,0.005248702,0.00014465717,0.0005475708,0.93727314,0.0003724316,0.00039796263,0.0076214396],"study_design_scores_gemma":[0.000052826967,0.00014919847,0.87861645,0.000042080395,0.00034366196,0.018611027,0.0002713438,0.0026270417,0.09596556,0.00072227215,0.0025656957,0.00003280276],"about_ca_topic_score_codex":0.0012336617,"about_ca_topic_score_gemma":0.002925587,"teacher_disagreement_score":0.0018121989,"about_ca_system_score_codex":0.0001502294,"about_ca_system_score_gemma":0.00015855063,"threshold_uncertainty_score":0.0060623884},"labels":[],"label_agreement":null},{"id":"W2055222883","doi":"10.1038/ng0207-153","title":"Human Genome Variation 2006: emerging views on structural variation and large-scale SNP analysis","year":2007,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Genetic Associations and Epidemiology","field":"Biochemistry, Genetics and Molecular Biology","cited_by":26,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"SickKids Foundation; Hospital for Sick Children; University of Toronto","funders":"","keywords":"Biology; Variation (astronomy); Structural variation; Human genetic variation; Genetic variation; Genome; Human genome; Copy-number variation; Genome-wide association study; Genetics; Evolutionary biology; SNP array; SNP; Computational biology; Single-nucleotide polymorphism; Gene; Genotype","score_opus":0.00973166044719661,"score_gpt":0.30218457142645927,"score_spread":0.2924529109792627,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2055222883","genre_codex":"methods","genre_gemma":"review","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"review","genre_consensus":null,"domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.042416357,0.2868152,0.40074548,0.24735424,0.0040779505,0.000041260653,0.0011625334,0.0005422067,0.01684475],"genre_scores_gemma":[0.6178202,0.16568047,0.12301826,0.06735722,0.02073408,0.00012986356,0.0008403976,0.00032458478,0.004095011],"study_design_codex":"theoretical_or_conceptual","study_design_gemma":"not_applicable","domain_scores_codex":[0.9963779,0.0014912734,0.00016194722,0.0008370649,0.0009818489,0.00015002572],"domain_scores_gemma":[0.97656107,0.017691921,0.00097389164,0.0024937154,0.0014951415,0.00078425964],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.016178802,0.0005132295,0.0015066204,0.0016175153,0.00080403493,0.00445038,0.0015664523,0.0028818385,0.002035034],"category_scores_gemma":[0.020936787,0.0005880035,0.0006274015,0.0031027189,0.008061683,0.007792285,0.0027424882,0.005985741,0.00032811845],"study_design_candidate":"not_applicable","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00032819438,0.000073162875,0.03498568,0.00077563094,0.0005501665,0.00029369423,0.0009984765,0.004792861,0.0059694843,0.56364167,0.028980412,0.35861057],"study_design_scores_gemma":[0.00003575932,0.000039978706,0.018984742,0.00028298545,0.00012280884,0.00048752228,0.0004101733,0.0056740004,0.0008782768,0.9205752,0.052426204,0.000082450584],"about_ca_topic_score_codex":0.0023439685,"about_ca_topic_score_gemma":0.003987664,"teacher_disagreement_score":0.016178802,"about_ca_system_score_codex":0.0013387359,"about_ca_system_score_gemma":0.0015431194,"threshold_uncertainty_score":0.085562706},"labels":[],"label_agreement":null},{"id":"W2055571033","doi":"10.1038/ng1408","title":"Nonsense-mediated decay microarray analysis identifies mutations of EPHB2 in human prostate cancer","year":2004,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Axon Guidance and Neuronal Signaling","field":"Neuroscience","cited_by":193,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Lunenfeld-Tanenbaum Research Institute; Mount Sinai Hospital; McGill University; University of Toronto; Jewish General Hospital","funders":"","keywords":"Biology; Nonsense mutation; Cancer research; Genetics; Frameshift mutation; Missense mutation; Prostate cancer; Cancer; Mutation; Gene","score_opus":0.018826548434472422,"score_gpt":0.31018659339932847,"score_spread":0.29136004496485607,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2055571033","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99694,0.00026235497,0.0014255963,0.000079541205,0.000011200576,0.000009375977,0.0006670509,0.000045902874,0.0005589931],"genre_scores_gemma":[0.9971955,0.00015450062,0.0010425735,0.000044197383,0.0000041709836,0.000011215098,0.0006397345,0.000016567697,0.0008915844],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9998381,0.000014533903,0.0000104260835,0.00003996776,0.00006456756,0.000032394855],"domain_scores_gemma":[0.99986625,0.00004089858,0.000023145743,0.00001543818,0.00002632778,0.000027952954],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00011499631,0.00014485976,0.00021471427,0.00060634903,0.0003419055,0.0003069475,0.00015940832,0.00033763677,0.0011971656],"category_scores_gemma":[0.00030556647,0.00015881813,0.00021293384,0.00033262934,0.00019315607,0.00008489374,0.0001571429,0.0003119067,0.00028294898],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00015767122,0.000022747861,0.005878139,0.00001708976,0.000014860561,0.00022420223,0.000029101393,0.00012648957,0.99133897,0.00010579186,0.00013561294,0.0019493978],"study_design_scores_gemma":[0.00002967323,0.00032157794,0.4142578,0.000008146011,0.0001299953,0.006015168,0.00021951848,0.0053758034,0.5690373,0.00037108734,0.0042117694,0.000022253045],"about_ca_topic_score_codex":0.0030830735,"about_ca_topic_score_gemma":0.006430771,"teacher_disagreement_score":0.0030830735,"about_ca_system_score_codex":0.0002931967,"about_ca_system_score_gemma":0.00025148346,"threshold_uncertainty_score":0.006130278},"labels":[],"label_agreement":null},{"id":"W2056386643","doi":"10.1038/ng.2918","title":"Mutations in TJP2 cause progressive cholestatic liver disease","year":2014,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Drug Transport and Resistance Mechanisms","field":"Medicine","cited_by":293,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Hospital for Sick Children; University of Toronto","funders":"National Institute of Diabetes and Digestive and Kidney Diseases; National Center for Advancing Translational Sciences; National Human Genome Research Institute","keywords":"Biology; Liver disease; Cholestasis; Gene; Mutation; Progressive familial intrahepatic cholestasis; Genetics; Disease; Pathophysiology; Bioinformatics; Liver transplantation; Pathology; Endocrinology; Internal medicine; Biochemistry","score_opus":0.008304630537718589,"score_gpt":0.2724065980170311,"score_spread":0.2641019674793125,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2056386643","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9812955,0.0016424964,0.005112227,0.0019115354,0.00038822272,0.000046139074,0.0009671285,0.00039091925,0.008245801],"genre_scores_gemma":[0.99663,0.00033301912,0.0010628103,0.00018227386,0.00009477874,0.000011137177,0.00022590822,0.000071372524,0.0013886044],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.99981815,0.000028768816,0.000022327215,0.000041072028,0.00006003964,0.000029676405],"domain_scores_gemma":[0.99967086,0.00009047815,0.000091192735,0.00001966772,0.000026514466,0.00010138108],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00013770584,0.0011605826,0.0004097465,0.0007703203,0.00049495837,0.00052616105,0.00048551295,0.0015789241,0.0038945598],"category_scores_gemma":[0.00055516575,0.00025578684,0.00049036,0.00060954166,0.0008905656,0.00032151776,0.000741313,0.00090830016,0.00076598796],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.001343293,0.00017287837,0.018038377,0.00022807869,0.0002642877,0.16269487,0.00033581557,0.0012173859,0.79440796,0.0033212057,0.003618739,0.014357046],"study_design_scores_gemma":[0.0007462242,0.0008279986,0.13566072,0.00016956496,0.0007848246,0.5111581,0.00073161826,0.011081233,0.29545525,0.0059703887,0.03721846,0.00019556454],"about_ca_topic_score_codex":0.0009497545,"about_ca_topic_score_gemma":0.0009377028,"teacher_disagreement_score":0.0038945598,"about_ca_system_score_codex":0.00031652593,"about_ca_system_score_gemma":0.0002907485,"threshold_uncertainty_score":0.013028622},"labels":[],"label_agreement":null},{"id":"W2056881795","doi":"10.1038/ng.2251","title":"A genome-wide association study identifies susceptibility loci for Wilms tumor","year":2012,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Renal and related cancers","field":"Biochemistry, Genetics and Molecular Biology","cited_by":81,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Alberta","funders":"CHILDREN with CANCER UK; National Institute of Environmental Health Sciences; National Institute for Health and Care Research; National Center for Advancing Translational Sciences; Rosetrees Trust; Government of the United Kingdom; Scottish Government; National Cancer Institute; Cancer Research UK; Wellcome Trust","keywords":"Wilms' tumor; Biology; Single-nucleotide polymorphism; Genetics; Genome-wide association study; Carcinogenesis; Malignancy; Genetic association; Cancer; Gene; Genotype","score_opus":0.0062062033336342205,"score_gpt":0.26037042254390663,"score_spread":0.25416421921027244,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2056881795","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99862945,0.00028844312,0.00039294967,0.0001051254,0.000013721839,0.0000046831397,0.000223624,0.000017110588,0.00032505437],"genre_scores_gemma":[0.99904865,0.0001230916,0.00033302282,0.000031689964,0.000016533382,0.000004433189,0.00018410606,0.000008126371,0.00025036628],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99951315,0.0001497229,0.00004458905,0.00013986594,0.0000939295,0.00005880436],"domain_scores_gemma":[0.9987643,0.0004618423,0.00027388422,0.00014490608,0.00009193774,0.0002632816],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00078322453,0.0004827963,0.00032863062,0.0013341754,0.000826905,0.0005553206,0.0004356613,0.00059982395,0.0017327542],"category_scores_gemma":[0.0016239485,0.0003667037,0.0005982102,0.0013235405,0.0005527157,0.00022268097,0.0005537738,0.0007920227,0.00017522686],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0034527634,0.00038150052,0.8809705,0.000062001796,0.0012616771,0.0027858482,0.0003260296,0.00019740975,0.1030277,0.00035088608,0.0005764894,0.006607221],"study_design_scores_gemma":[0.000113118644,0.00025655524,0.9921234,0.000005434274,0.0005396126,0.0023300108,0.00012887176,0.00031922638,0.0033450408,0.00016498174,0.0006609227,0.000012731165],"about_ca_topic_score_codex":0.0024339317,"about_ca_topic_score_gemma":0.0032473386,"teacher_disagreement_score":0.0024339317,"about_ca_system_score_codex":0.00020446694,"about_ca_system_score_gemma":0.00036114754,"threshold_uncertainty_score":0.005796671},"labels":[],"label_agreement":null},{"id":"W2058880763","doi":"10.1038/ng1943","title":"The neuronal sortilin-related receptor SORL1 is genetically associated with Alzheimer disease","year":2007,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Alzheimer's disease research and treatments","field":"Medicine","cited_by":1169,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Toronto Western Hospital; Occupational Cancer Research Centre; University of Toronto","funders":"National Institute on Aging","keywords":"Biology; Alzheimer's disease; Amyloid precursor protein; Gene; Receptor; Genetics; Disease","score_opus":0.015838220532540727,"score_gpt":0.30576228246431014,"score_spread":0.2899240619317694,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2058880763","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.996207,0.0006874984,0.0011494238,0.0003617352,0.00006883407,0.000012323146,0.00039436755,0.00006305964,0.0010556642],"genre_scores_gemma":[0.996833,0.000319427,0.001076623,0.00011506546,0.00006691793,0.000009441797,0.00026815027,0.0000484619,0.001262818],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.99944896,0.0001487837,0.00007851484,0.0001503956,0.00013011038,0.00004318644],"domain_scores_gemma":[0.9983027,0.0003337206,0.000982581,0.000074805204,0.00009015153,0.00021588003],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00039825332,0.0011637178,0.0005648989,0.0015634187,0.00063952163,0.0005413974,0.0006501024,0.0014152115,0.0039052109],"category_scores_gemma":[0.0010916434,0.00035960323,0.0005404936,0.0007130114,0.00082959194,0.00027841082,0.00074100087,0.0009591568,0.00059656723],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.007502187,0.00039148564,0.084504545,0.00034993124,0.0008402792,0.034426637,0.0005657838,0.0010280873,0.85422474,0.0024590958,0.0021810476,0.011526134],"study_design_scores_gemma":[0.0007200377,0.0011687864,0.72453195,0.00020521012,0.0017281027,0.14745137,0.0008118633,0.0075686933,0.09981234,0.004461728,0.01132904,0.00021081288],"about_ca_topic_score_codex":0.0009371325,"about_ca_topic_score_gemma":0.00085112953,"teacher_disagreement_score":0.0039052109,"about_ca_system_score_codex":0.00034746074,"about_ca_system_score_gemma":0.00027141714,"threshold_uncertainty_score":0.013064206},"labels":[],"label_agreement":null},{"id":"W2059154675","doi":"10.1038/ng.2931","title":"Germline and somatic SMARCA4 mutations characterize small cell carcinoma of the ovary, hypercalcemic type","year":2014,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Chromatin Remodeling and Cancer","field":"Biochemistry, Genetics and Molecular Biology","cited_by":500,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University Health Network; Royal Victoria Hospital; Royal Victoria Regional Health Centre; Jewish General Hospital; McGill University; University of Ottawa; McGill University Health Centre; Princess Margaret Cancer Centre; Montreal Children's Hospital; McGill University and Génome Québec Innovation Centre; Children's Hospital of Eastern Ontario; McGill Genome Centre","funders":"National Heart, Lung, and Blood Institute","keywords":"SMARCA4; Biology; Germline; Germline mutation; Genetics; Somatic cell; Mutation; Exome sequencing; Cancer research; Epigenetics; Gene","score_opus":0.007905791056056787,"score_gpt":0.2248158149058023,"score_spread":0.2169100238497455,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2059154675","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99840146,0.00015854785,0.0001412357,0.00004410506,0.0000047440476,0.000008867808,0.0001369781,0.000016841323,0.0010871715],"genre_scores_gemma":[0.9993389,0.000054622276,0.00015379213,0.00001289518,0.0000073799383,0.0000032511468,0.000087137945,0.000009417307,0.00033261263],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9997929,0.000014556299,0.000022183895,0.000045029472,0.000062875144,0.000062448766],"domain_scores_gemma":[0.9995523,0.000124399,0.00014023914,0.00004024591,0.000029124154,0.00011372431],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00013915278,0.00057431357,0.00038075686,0.0017406009,0.00042120193,0.00056690816,0.0005883861,0.00085000426,0.0025664505],"category_scores_gemma":[0.0010298804,0.00036176073,0.0003523192,0.0011651181,0.0008218407,0.00024647688,0.00038752894,0.00032489764,0.00038827275],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0017424662,0.00015381793,0.34378916,0.00008890727,0.00014772733,0.17308088,0.00065653614,0.00067360315,0.4699198,0.0012473597,0.00047852154,0.008021117],"study_design_scores_gemma":[0.000138332,0.00040397298,0.588915,0.000009820631,0.00014051844,0.36707166,0.00070095295,0.0012781278,0.038333315,0.0010708993,0.0018978497,0.00003964526],"about_ca_topic_score_codex":0.0023381505,"about_ca_topic_score_gemma":0.0030467515,"teacher_disagreement_score":0.0025664505,"about_ca_system_score_codex":0.0004853371,"about_ca_system_score_gemma":0.00030667812,"threshold_uncertainty_score":0.008585632},"labels":[],"label_agreement":null},{"id":"W2059171091","doi":"10.1038/ng1364","title":"Cornelia de Lange syndrome is caused by mutations in NIPBL, the human homolog of Drosophila melanogaster Nipped-B","year":2004,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Genomics and Chromatin Dynamics","field":"Biochemistry, Genetics and Molecular Biology","cited_by":722,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"McMaster University Medical Centre","funders":"Eunice Kennedy Shriver National Institute of Child Health and Human Development; National Institutes of Health; Children's Hospital of Philadelphia; National Institute of Child Health and Human Development; Cornelia de Lange Syndrome Foundation","keywords":"Cornelia de Lange Syndrome; Biology; Genetics; Drosophila melanogaster; Gene","score_opus":0.005532571241905298,"score_gpt":0.23889710539433495,"score_spread":0.23336453415242966,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2059171091","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9784822,0.0031275179,0.0060927626,0.0009927669,0.0004823212,0.00013905071,0.0014627059,0.0010283043,0.008192355],"genre_scores_gemma":[0.9895716,0.0010721601,0.003860908,0.00022787366,0.00016262736,0.000045197816,0.00048096335,0.00012691513,0.0044518146],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99935716,0.00007694233,0.000062853556,0.00014988112,0.0002699072,0.0000831783],"domain_scores_gemma":[0.9983975,0.00057488243,0.00056646566,0.00006171207,0.00006722307,0.0003321979],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00028873413,0.0029579843,0.0008146612,0.0023892666,0.00092932826,0.0007148192,0.0008374578,0.0029034284,0.0034899754],"category_scores_gemma":[0.0016076189,0.000598632,0.0005147475,0.0011743524,0.0018772323,0.0006150942,0.001410959,0.0015974683,0.0009497567],"study_design_candidate":"bench_or_experimental","study_design_consensus":"bench_or_experimental","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00092621765,0.00017520032,0.0074012903,0.00043576094,0.00020717247,0.2145821,0.00035831062,0.0009134023,0.75383925,0.0032909324,0.0023289705,0.015541429],"study_design_scores_gemma":[0.00094823074,0.00070861704,0.097552225,0.00021163267,0.0005565156,0.6726555,0.00040459214,0.0059471475,0.18978955,0.004157434,0.026727464,0.0003410938],"about_ca_topic_score_codex":0.0020403224,"about_ca_topic_score_gemma":0.003033109,"teacher_disagreement_score":0.0034899754,"about_ca_system_score_codex":0.00071609963,"about_ca_system_score_gemma":0.00078005076,"threshold_uncertainty_score":0.011675119},"labels":[],"label_agreement":null},{"id":"W2059706140","doi":"10.1038/ng1605","title":"Plk4 haploinsufficiency causes mitotic infidelity and carcinogenesis","year":2005,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Microtubule and mitosis dynamics","field":"Biochemistry, Genetics and Molecular Biology","cited_by":206,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Lunenfeld-Tanenbaum Research Institute; University of Toronto; University of Windsor; Mount Sinai Hospital","funders":"","keywords":"Biology; Mitosis; Haploinsufficiency; Cell biology; Carcinogenesis; Cell cycle; Loss of heterozygosity; Cancer research; Genetics; Cell; Cancer; Gene; Phenotype","score_opus":0.0062962445545472374,"score_gpt":0.24377015571810834,"score_spread":0.2374739111635611,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2059706140","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.991115,0.00096912973,0.0026966073,0.00041195555,0.00008461364,0.0000463717,0.001094089,0.00039460216,0.003187628],"genre_scores_gemma":[0.9940117,0.00038269584,0.00090153364,0.00007587266,0.000013590394,0.000025834419,0.00037052023,0.00008397802,0.0041341595],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9996824,0.00004702557,0.00004750685,0.00006889659,0.00007552549,0.00007860242],"domain_scores_gemma":[0.9995117,0.00010745674,0.00011636786,0.000095625335,0.000025326206,0.00014338725],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00023773023,0.00061616354,0.00043775173,0.0011529811,0.0004961745,0.0007153698,0.0006004105,0.0007157203,0.005984053],"category_scores_gemma":[0.00031445743,0.0005778108,0.00037213753,0.0004800025,0.0006098979,0.00031326502,0.00073876046,0.0011954415,0.00086579163],"study_design_candidate":"bench_or_experimental","study_design_consensus":"bench_or_experimental","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0003480031,0.000065814194,0.0007068993,0.000039041475,0.000016863745,0.0005363483,0.000019399282,0.0003395541,0.9950045,0.0006590358,0.0002418203,0.002022709],"study_design_scores_gemma":[0.000049155835,0.0001457444,0.0058665327,0.000008665159,0.000034145214,0.0016800292,0.0000578606,0.001808551,0.9864703,0.00028400004,0.0035842317,0.00001087041],"about_ca_topic_score_codex":0.0016636953,"about_ca_topic_score_gemma":0.0018664561,"teacher_disagreement_score":0.005984053,"about_ca_system_score_codex":0.0005995493,"about_ca_system_score_gemma":0.00051739597,"threshold_uncertainty_score":0.020018578},"labels":[],"label_agreement":null},{"id":"W2059742736","doi":"10.1038/ng.2007.16","title":"A survey of genetic human cortical gene expression","year":2007,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Gene expression and cancer classification","field":"Biochemistry, Genetics and Molecular Biology","cited_by":488,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Kronos (Canada)","funders":"National Institute of Neurological Disorders and Stroke; National Institute of Mental Health; National Heart, Lung, and Blood Institute; National Institute on Aging","keywords":"Biology; Genotyping; Transcriptome; Genetics; SNP genotyping; Gene expression; Computational biology; Gene; SNP array; DNA microarray; Gene expression profiling; Human genome; Genome; Genomics; Human brain; Human genetics; Genome-wide association study; Genotype; Single-nucleotide polymorphism; Neuroscience","score_opus":0.016856165160706465,"score_gpt":0.31083293400235956,"score_spread":0.2939767688416531,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2059742736","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.964806,0.012429203,0.0058958447,0.00036179065,0.000019081643,0.000011317743,0.004612567,0.00012544583,0.011738742],"genre_scores_gemma":[0.9830918,0.008121258,0.0017407162,0.000108932014,0.000018338555,0.000016314692,0.0033419789,0.000048697944,0.003512052],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9998847,0.0000223596,0.000007940213,0.000032418808,0.00003056408,0.000021966558],"domain_scores_gemma":[0.99952495,0.0002008862,0.000038772585,0.000042916436,0.00013694822,0.000055680335],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00023494734,0.00014095055,0.00017601055,0.0018948988,0.00029500635,0.00032900428,0.00014892068,0.000109901506,0.0026379253],"category_scores_gemma":[0.0006117465,0.000081240105,0.00012627947,0.0024522287,0.00025036905,0.00013856596,0.00019166838,0.00017114707,0.0004909961],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0009883393,0.00006160002,0.23370427,0.0005307709,0.0002398309,0.0014176099,0.0008188035,0.0013918583,0.5193648,0.0055324426,0.005063944,0.2308858],"study_design_scores_gemma":[0.000013630115,0.00015158154,0.8659795,0.00004201407,0.00012979475,0.005214566,0.00063184585,0.0011095713,0.08074635,0.0024053685,0.043551113,0.000024636456],"about_ca_topic_score_codex":0.006231436,"about_ca_topic_score_gemma":0.008107323,"teacher_disagreement_score":0.006231436,"about_ca_system_score_codex":0.00039917047,"about_ca_system_score_gemma":0.000462384,"threshold_uncertainty_score":0.0123903155},"labels":[],"label_agreement":null},{"id":"W2060428411","doi":"10.1038/ng.2787","title":"Thread 2: Network models","year":2013,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Simulation Techniques and Applications","field":"Decision Sciences","cited_by":2,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Nature Conservancy of Canada; University of Toronto","funders":"","keywords":"Biology; Thread (computing); Computational biology; Computer science; Operating system","score_opus":0.08584405768507898,"score_gpt":0.40051485857953045,"score_spread":0.3146708008944515,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2060428411","genre_codex":"methods","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":null,"domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.0140535645,0.00044949408,0.92310154,0.0035042625,0.00036864344,0.00019810822,0.0052796523,0.0019514066,0.051093355],"genre_scores_gemma":[0.50677156,0.0019306476,0.39363012,0.0012637165,0.00091304333,0.0015906615,0.0103867175,0.0019360296,0.08157755],"study_design_codex":"theoretical_or_conceptual","study_design_gemma":"simulation_or_modeling","domain_scores_codex":[0.9992079,0.0002817579,0.000037050067,0.00017509202,0.00021007334,0.000088050365],"domain_scores_gemma":[0.9978077,0.0011147568,0.00016813075,0.00036919056,0.00036207517,0.00017824386],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0013313175,0.00070881366,0.0007674013,0.0007891945,0.0007075614,0.0025583182,0.0021769044,0.0020152444,0.027640348],"category_scores_gemma":[0.0080169905,0.00053574913,0.0014685343,0.00081535196,0.00065995665,0.003437256,0.0015930738,0.0019066283,0.0050397967],"study_design_candidate":"simulation_or_modeling","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.000103325656,0.00006577375,0.0010693889,0.000113294074,0.000057219386,0.00014490118,0.00013440716,0.4547021,0.00079709105,0.49769527,0.024656186,0.020460984],"study_design_scores_gemma":[0.00003700323,0.000014786513,0.00012528505,0.000021233325,0.0000147542,0.000040558167,0.000019687457,0.6956818,0.00020993088,0.2817753,0.022049636,0.000010108039],"about_ca_topic_score_codex":0.007568415,"about_ca_topic_score_gemma":0.00662129,"teacher_disagreement_score":0.027640348,"about_ca_system_score_codex":0.0011404674,"about_ca_system_score_gemma":0.0016135167,"threshold_uncertainty_score":0.092466176},"labels":[],"label_agreement":null},{"id":"W2061151633","doi":"10.1038/ng1390","title":"An X-to-autosome retrogene is required for spermatogenesis in mice","year":2004,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Genomics and Chromatin Dynamics","field":"Biochemistry, Genetics and Molecular Biology","cited_by":104,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"McGill University and Génome Québec Innovation Centre","funders":"","keywords":"Biology; Genetics; Gene; Frameshift mutation; Exon; Intron; Untranslated region; Coding region; Messenger RNA","score_opus":0.0059594449233114875,"score_gpt":0.2560769299657234,"score_spread":0.25011748504241194,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2061151633","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.985355,0.0016163547,0.008628421,0.00025606685,0.00007737208,0.00005589636,0.0011966657,0.00068833976,0.0021258479],"genre_scores_gemma":[0.9889092,0.0006047394,0.0036247603,0.00013791728,0.000032022366,0.000051833285,0.0007628674,0.00043201575,0.005444579],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9993788,0.00008777179,0.00010262365,0.00016836786,0.00017524626,0.00008726125],"domain_scores_gemma":[0.9982108,0.00035876257,0.00079000776,0.0002046834,0.00006212097,0.00037368285],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00039297368,0.00085784803,0.00051224936,0.0014154986,0.00050029537,0.0008418065,0.00095591036,0.0012976483,0.0032886316],"category_scores_gemma":[0.00039715442,0.0009406853,0.00075135933,0.00040552756,0.0009571849,0.00054153654,0.0007646359,0.0017476518,0.0012744969],"study_design_candidate":"bench_or_experimental","study_design_consensus":"bench_or_experimental","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.000117259224,0.000016914653,0.000274862,0.000020295762,0.000009772454,0.00021090906,0.000013721529,0.000062073654,0.9986136,0.00020353963,0.000018482498,0.00043866993],"study_design_scores_gemma":[0.00007360532,0.00015753375,0.008433997,0.000016498323,0.000061889565,0.001304971,0.000052783704,0.00088726304,0.987015,0.00017646325,0.0018057062,0.000014210133],"about_ca_topic_score_codex":0.000695898,"about_ca_topic_score_gemma":0.0010544157,"teacher_disagreement_score":0.0032886316,"about_ca_system_score_codex":0.00052273506,"about_ca_system_score_gemma":0.00033914478,"threshold_uncertainty_score":0.011001527},"labels":[],"label_agreement":null},{"id":"W2061169804","doi":"10.1038/ng.822","title":"Mutations in CEP57 cause mosaic variegated aneuploidy syndrome","year":2011,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Microtubule and mitosis dynamics","field":"Biochemistry, Genetics and Molecular Biology","cited_by":169,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Hospital for Sick Children; SickKids Foundation; Mount Sinai Hospital","funders":"National Institute for Health and Care Research; Cancer Research UK","keywords":"Biology; Aneuploidy; Genetics; Mutation; Loss function; Function (biology); Mosaic; Kinetochore; Exome sequencing; Computational biology; Chromosome; Phenotype; Gene","score_opus":0.009799501253133681,"score_gpt":0.23878690275722791,"score_spread":0.22898740150409425,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2061169804","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99213094,0.00066198746,0.0029884905,0.0002661171,0.0001548836,0.000016676428,0.0004403706,0.00016062244,0.0031798407],"genre_scores_gemma":[0.9973053,0.00027235685,0.0010796975,0.000043419706,0.00003295381,0.000008374425,0.00013208909,0.000056138444,0.0010695844],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9997696,0.000020896794,0.000035524987,0.000048160928,0.00009160333,0.000034118788],"domain_scores_gemma":[0.9992612,0.00026043365,0.00020063296,0.00006514791,0.000035355577,0.00017722066],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00015119683,0.0010985023,0.00052996876,0.0011989584,0.00044850836,0.00039988573,0.00074353494,0.0012762363,0.003551905],"category_scores_gemma":[0.0009710348,0.00039208325,0.00037875937,0.00067185285,0.0008084453,0.0003277733,0.0009277575,0.000693542,0.00059100636],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.000813195,0.00011894725,0.015373614,0.000113509785,0.0002350798,0.22549838,0.00030758895,0.0018513803,0.73474294,0.0046284175,0.0013213161,0.014995658],"study_design_scores_gemma":[0.00046138465,0.000344901,0.11726775,0.00008966923,0.00048958644,0.45184305,0.00051965436,0.010240811,0.40018418,0.0048984312,0.013510023,0.00015059148],"about_ca_topic_score_codex":0.0016633177,"about_ca_topic_score_gemma":0.0020875302,"teacher_disagreement_score":0.003551905,"about_ca_system_score_codex":0.00047036525,"about_ca_system_score_gemma":0.00035889226,"threshold_uncertainty_score":0.011882305},"labels":[],"label_agreement":null},{"id":"W2062278718","doi":"10.1038/ng876","title":"Genetic evidence that oxidative derivatives of retinoic acid are not involved in retinoid signaling during mouse development","year":2002,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Retinoids in leukemia and cellular processes","field":"Biochemistry, Genetics and Molecular Biology","cited_by":233,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Queen's University","funders":"National Cancer Institute; Canadian Institutes of Health Research; Fondation pour la Recherche Médicale; Institut National de la Santé et de la Recherche Médicale; Centre National de la Recherche Scientifique; Association pour la Recherche sur le Cancer; Bristol-Myers Squibb","keywords":"Retinoic acid; Biology; Tretinoin; Retinoic acid-inducible orphan G protein-coupled receptor; Basigin; Cell biology; Haploinsufficiency; Retinoic acid receptor; Genetics; Phenotype; Cell culture; Gene","score_opus":0.024543795040948075,"score_gpt":0.24831003459721673,"score_spread":0.22376623955626865,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2062278718","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.97519106,0.0027741855,0.012389917,0.0005172072,0.00008463205,0.000040531377,0.0014622388,0.00044046962,0.007099792],"genre_scores_gemma":[0.97936946,0.0014095918,0.0056880848,0.00015686917,0.00002021054,0.000055656943,0.0012160228,0.00027251235,0.011811585],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99932575,0.00010289788,0.00008864365,0.00017588741,0.0001714305,0.00013542232],"domain_scores_gemma":[0.9980019,0.00041790248,0.00081092794,0.00030877034,0.00013883777,0.00032170664],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0004785531,0.00078533246,0.00036764247,0.0020618357,0.00045780904,0.0009669786,0.00097609137,0.001141831,0.0036085816],"category_scores_gemma":[0.00053782103,0.0009928335,0.0005389107,0.00049933104,0.0011402875,0.0007840407,0.00051006995,0.001619541,0.0011524508],"study_design_candidate":"bench_or_experimental","study_design_consensus":"bench_or_experimental","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00019544899,0.000008982605,0.00035703514,0.000014825358,0.0000068066656,0.00011221937,0.000015721245,0.00003598539,0.99806374,0.0006172872,0.00002197137,0.0005499643],"study_design_scores_gemma":[0.000022019327,0.000060282662,0.0043326304,0.000010420972,0.00004232691,0.00049434486,0.00003631627,0.00021458062,0.9925047,0.00027935815,0.0019967342,0.0000062860795],"about_ca_topic_score_codex":0.0014251182,"about_ca_topic_score_gemma":0.0025369797,"teacher_disagreement_score":0.0036085816,"about_ca_system_score_codex":0.0008188612,"about_ca_system_score_gemma":0.0004537351,"threshold_uncertainty_score":0.0120719075},"labels":[],"label_agreement":null},{"id":"W2062532725","doi":"10.1038/ng.410","title":"Genome-wide association study identifies variants at 9p21 and 22q13 associated with development of cutaneous nevi","year":2009,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Cutaneous Melanoma Detection and Management","field":"Medicine","cited_by":226,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"McGill University; McGill University and Génome Québec Innovation Centre","funders":"National Cancer Institute; National Institute for Health and Care Research; Cancer Research UK; Wellcome Trust","keywords":"CDKN2A; Genome-wide association study; Melanoma; Biology; Locus (genetics); Single-nucleotide polymorphism; Nevus; Genetics; Genetic association; Genetic predisposition; Dermatology; Gene; Genotype; Medicine","score_opus":0.007499940298086891,"score_gpt":0.236489020011754,"score_spread":0.2289890797136671,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2062532725","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99807715,0.0005557358,0.00024050777,0.0001164711,0.000019036936,0.000010759357,0.00022867418,0.000018522547,0.0007331813],"genre_scores_gemma":[0.99905616,0.00017886405,0.00019991536,0.000025921114,0.00002120961,0.0000061051,0.00013112907,0.000007987788,0.0003726226],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99909985,0.00025185433,0.00009646184,0.0002465968,0.00021682978,0.00008831279],"domain_scores_gemma":[0.9978123,0.0008112909,0.0007802421,0.0001404131,0.00016881467,0.00028704022],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0007726954,0.0007019777,0.0004936031,0.0021852446,0.0008050669,0.0007876817,0.00079111755,0.0009380834,0.0026477983],"category_scores_gemma":[0.0031413173,0.00046879263,0.00072252954,0.0017424388,0.00052327366,0.00029514448,0.00058584893,0.0009303188,0.00026044407],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0020336665,0.00025761776,0.95560884,0.000054481974,0.00097515876,0.0061677494,0.0002288823,0.00019816105,0.026298659,0.00018400086,0.0005228781,0.0074699563],"study_design_scores_gemma":[0.000051359362,0.000114921466,0.99385154,0.000007895391,0.0003050579,0.0039760065,0.000067629364,0.00028585613,0.00090875867,0.000089472764,0.00033207994,0.000009394474],"about_ca_topic_score_codex":0.003745746,"about_ca_topic_score_gemma":0.0043319403,"teacher_disagreement_score":0.003745746,"about_ca_system_score_codex":0.0002547962,"about_ca_system_score_gemma":0.00034137545,"threshold_uncertainty_score":0.008857727},"labels":[],"label_agreement":null},{"id":"W2062992807","doi":"10.1038/ng1104-1131","title":"Reply to \"Genomic Control to the extreme\"","year":2004,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Genetic Associations and Epidemiology","field":"Biochemistry, Genetics and Molecular Biology","cited_by":7,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"McGill University; McGill Genome Centre","funders":"","keywords":"Biology; Computational biology; Genetics; Evolutionary biology","score_opus":0.009047945107718908,"score_gpt":0.2567504553986209,"score_spread":0.24770251029090198,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2062992807","genre_codex":"commentary","genre_gemma":"commentary","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"commentary","genre_consensus":"commentary","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.000121638455,0.0019671672,0.00020276567,0.96450704,0.03287785,0.0000021720018,0.00004375891,0.00001966006,0.00025798302],"genre_scores_gemma":[0.001740883,0.0008972059,0.00019108428,0.9432974,0.053016305,0.000012125993,0.000025185353,0.00001784552,0.0008019257],"study_design_codex":"not_applicable","study_design_gemma":"not_applicable","domain_scores_codex":[0.99421895,0.0018991879,0.00074686576,0.0012688565,0.0012469685,0.0006191821],"domain_scores_gemma":[0.9553901,0.03137531,0.0016797169,0.0020347459,0.006014629,0.0035056013],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.011551281,0.0015677297,0.0026914596,0.0014022887,0.004353469,0.004726935,0.004418611,0.04465928,0.006441379],"category_scores_gemma":[0.055210847,0.0012389643,0.0014287172,0.001392083,0.010935028,0.0072703552,0.005271446,0.06818066,0.0041793953],"study_design_candidate":"not_applicable","study_design_consensus":"not_applicable","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00007430923,0.000017965263,0.00040227085,0.000100584024,0.000051467985,0.0002663683,0.00027940617,0.000076269156,0.00013980673,0.0076663163,0.9857077,0.0052176234],"study_design_scores_gemma":[0.0003371222,0.000058662445,0.002952418,0.00071317743,0.00012024098,0.0010924422,0.0014857652,0.00040224148,0.0005187131,0.062136516,0.9299988,0.00018379849],"about_ca_topic_score_codex":0.0038198777,"about_ca_topic_score_gemma":0.004429101,"teacher_disagreement_score":0.04465928,"about_ca_system_score_codex":0.0023641258,"about_ca_system_score_gemma":0.0033877222,"threshold_uncertainty_score":0.061089694},"labels":[],"label_agreement":null},{"id":"W2063662864","doi":"10.1038/ng.2532","title":"The genomic landscape of hypodiploid acute lymphoblastic leukemia","year":2013,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Acute Lymphoblastic Leukemia research","field":"Medicine","cited_by":728,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Princess Margaret Cancer Centre; University of Toronto; University Health Network","funders":"National Institute of General Medical Sciences; National Cancer Institute","keywords":"Biology; Aneuploidy; Cancer research; Bruton's tyrosine kinase; Exome sequencing; Receptor tyrosine kinase; Genetics; Signal transduction; Leukemia; Exome; Tyrosine kinase; Gene; Chromosome; Mutation","score_opus":0.006995370297557125,"score_gpt":0.2575525198971469,"score_spread":0.25055714959958975,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2063662864","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.97818977,0.0069414787,0.0016906855,0.0041813394,0.0000348729,0.0000101991145,0.00084995665,0.00006915583,0.008032557],"genre_scores_gemma":[0.99585575,0.0021591766,0.00032505763,0.0005028813,0.00006356685,0.0000055537735,0.00028741057,0.000021714952,0.0007789484],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9997787,0.000053126707,0.000009469012,0.000056845343,0.000053807515,0.000048200374],"domain_scores_gemma":[0.9996991,0.000115348324,0.00008967501,0.000019808134,0.000026750382,0.000049429254],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0001827513,0.00014552845,0.00023897721,0.0008139546,0.00027363165,0.0008424469,0.0003155241,0.00036368455,0.0035984516],"category_scores_gemma":[0.0009567423,0.00015365188,0.0000900601,0.0007630043,0.00047268948,0.0005066106,0.00056616944,0.00047730372,0.0003482457],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0019186175,0.00010961491,0.2692672,0.00040777563,0.00024509357,0.0054291375,0.0014191245,0.006345946,0.4621689,0.028514456,0.0067490847,0.21742497],"study_design_scores_gemma":[0.00011954149,0.0005132178,0.8077367,0.00013448743,0.00038085465,0.01642592,0.0027729245,0.0046261353,0.03030368,0.08116115,0.05576433,0.000061016755],"about_ca_topic_score_codex":0.0005414635,"about_ca_topic_score_gemma":0.00078422076,"teacher_disagreement_score":0.0035984516,"about_ca_system_score_codex":0.00037010916,"about_ca_system_score_gemma":0.00019800136,"threshold_uncertainty_score":0.0120379925},"labels":[],"label_agreement":null},{"id":"W2064041354","doi":"10.1038/ng.354","title":"Newly discovered breast cancer susceptibility loci on 3p24 and 17q23.2","year":2009,"lang":"en","type":"article","venue":"Nature Genetics","topic":"BRCA gene mutations in cancer","field":"Biochemistry, Genetics and Molecular Biology","cited_by":484,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Lunenfeld-Tanenbaum Research Institute; Cancer Care Ontario; Mount Sinai Hospital","funders":"National Cancer Institute; National Institutes of Health; Cancer Research UK; Wellcome Trust","keywords":"Genome-wide association study; Breast cancer; Biology; Allele; Genetics; Genetic association; Cancer; Oncology; Gene; Genotype; Single-nucleotide polymorphism; Medicine","score_opus":0.006138970997413633,"score_gpt":0.2820554783084042,"score_spread":0.2759165073109906,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2064041354","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.96650463,0.017236667,0.005200269,0.0020701683,0.0006006015,0.00005225733,0.001603551,0.00034699801,0.0063846996],"genre_scores_gemma":[0.9844906,0.0037930121,0.006313291,0.00028848302,0.00036600762,0.00005518763,0.00094565755,0.000051369097,0.0036964032],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.99980515,0.000022767155,0.00001190901,0.000047583962,0.00006843549,0.000044168755],"domain_scores_gemma":[0.9994948,0.00014083792,0.00018024305,0.00003179701,0.000048272144,0.00010398403],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00028526352,0.00073376234,0.00061568746,0.0018164009,0.00037838495,0.000795761,0.0010471601,0.0011384214,0.0051092748],"category_scores_gemma":[0.00086048484,0.00042815006,0.00064972887,0.001086185,0.00053582015,0.00027602236,0.0005223488,0.0008553903,0.00069214945],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.003243499,0.00030160235,0.11288832,0.0005095652,0.00073975255,0.16290428,0.0009801213,0.0028235423,0.60375214,0.013760774,0.008936118,0.089160286],"study_design_scores_gemma":[0.0011259746,0.000875218,0.4026042,0.00027859805,0.001547539,0.24437827,0.0009763092,0.00399344,0.19775541,0.024340026,0.121823646,0.00030132986],"about_ca_topic_score_codex":0.00101499,"about_ca_topic_score_gemma":0.0015079266,"teacher_disagreement_score":0.0051092748,"about_ca_system_score_codex":0.00046778907,"about_ca_system_score_gemma":0.0003434691,"threshold_uncertainty_score":0.017092228},"labels":[],"label_agreement":null},{"id":"W2064340631","doi":"10.1038/ng2099","title":"Genome-wide association study of restless legs syndrome identifies common variants in three genomic regions","year":2007,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Restless Legs Syndrome Research","field":"Medicine","cited_by":702,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"McGill University; Douglas Mental Health University Institute; Hôpital du Sacré-Cœur de Montréal; Université de Montréal; Hôpital Notre-Dame","funders":"","keywords":"Biology; Restless legs syndrome; Genetics; Genome-wide association study; Homeobox; Gene; Locus (genetics); Allele; Genetic association; Single-nucleotide polymorphism; Transcription factor; Genotype; Neuroscience","score_opus":0.030344068337002088,"score_gpt":0.33775613928881687,"score_spread":0.3074120709518148,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2064340631","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9969035,0.0006647198,0.0011687397,0.00017564642,0.000019443945,0.000012775581,0.00036570153,0.00002548977,0.00066398986],"genre_scores_gemma":[0.99882334,0.00010438727,0.00056754507,0.000063905776,0.000013386159,0.0000065928866,0.0001667738,0.000008465829,0.00024569043],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99941635,0.00012238156,0.00006998027,0.00019506318,0.00011892901,0.000077388446],"domain_scores_gemma":[0.9989999,0.00050668436,0.00021896725,0.000073726,0.00006396305,0.00013669717],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0005616069,0.00065108546,0.00046706304,0.0013719936,0.00063093915,0.0005245319,0.0006496849,0.00097547536,0.0022225217],"category_scores_gemma":[0.0012488954,0.00024922943,0.0008856015,0.0011618326,0.0007182105,0.00019250851,0.0005187416,0.00080229837,0.0002285167],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0073253433,0.0004359453,0.6965222,0.00016685286,0.0019703968,0.0121904705,0.00096527673,0.00077480695,0.2577744,0.0010983625,0.0010765812,0.019699417],"study_design_scores_gemma":[0.00035086012,0.0003764758,0.97898483,0.000024544433,0.0009956184,0.006294981,0.000270919,0.0007962707,0.010324639,0.0005807526,0.0009676737,0.00003237885],"about_ca_topic_score_codex":0.004927591,"about_ca_topic_score_gemma":0.006914239,"teacher_disagreement_score":0.004927591,"about_ca_system_score_codex":0.00022013129,"about_ca_system_score_gemma":0.00036390807,"threshold_uncertainty_score":0.009797871},"labels":[],"label_agreement":null},{"id":"W2064966510","doi":"10.1038/ng.366","title":"A common allele in RPGRIP1L is a modifier of retinal degeneration in ciliopathies","year":2009,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Genetic and Kidney Cyst Diseases","field":"Biochemistry, Genetics and Molecular Biology","cited_by":268,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"McGill University; McGill University Health Centre","funders":"Eunice Kennedy Shriver National Institute of Child Health and Human Development; National Institute of Diabetes and Digestive and Kidney Diseases; National Institutes of Health; National Eye Institute; Howard Hughes Medical Institute","keywords":"Ciliopathies; Biology; Retinitis pigmentosa; Joubert syndrome; Retinal degeneration; Genetics; Allele; Ciliopathy; Cilium; Nephronophthisis; Bardet–Biedl syndrome; Phenotype; Gene","score_opus":0.0058640703543445345,"score_gpt":0.25493430318624355,"score_spread":0.24907023283189902,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2064966510","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.97525406,0.0010616241,0.011172264,0.0019104298,0.00092935876,0.00022975112,0.002601472,0.0011497422,0.0056912377],"genre_scores_gemma":[0.9927861,0.000159388,0.0033381977,0.00042698884,0.00020523112,0.00008146257,0.00061797193,0.0002538005,0.0021309168],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.99869555,0.000227347,0.00023342254,0.0003863218,0.0003136431,0.00014376194],"domain_scores_gemma":[0.9979906,0.00058514025,0.0007059101,0.00018924952,0.000106028434,0.00042300273],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00053700834,0.001995951,0.0011324988,0.0020580483,0.0011680257,0.00055339094,0.0020789062,0.0033661968,0.011334852],"category_scores_gemma":[0.0018501459,0.0004936518,0.0018293052,0.00084264716,0.0015628671,0.00049572915,0.0015223484,0.0020894522,0.002311929],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0019392151,0.00025609956,0.005752961,0.00017512323,0.00039575435,0.09827234,0.0002524243,0.00050614926,0.88087577,0.0019418615,0.0019733303,0.0076589924],"study_design_scores_gemma":[0.0015543792,0.0018486801,0.16375826,0.00035921158,0.0017468582,0.40793234,0.00062479975,0.009986486,0.3903695,0.0033068683,0.018099012,0.00041360827],"about_ca_topic_score_codex":0.0023201208,"about_ca_topic_score_gemma":0.0023053521,"teacher_disagreement_score":0.011334852,"about_ca_system_score_codex":0.00074099697,"about_ca_system_score_gemma":0.0006410467,"threshold_uncertainty_score":0.037918925},"labels":[],"label_agreement":null},{"id":"W2065581872","doi":"10.1038/ng1261","title":"Heterozygous mutations of the kinesin KIF21A in congenital fibrosis of the extraocular muscles type 1 (CFEOM1)","year":2003,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Ophthalmology and Eye Disorders","field":"Medicine","cited_by":262,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Hospital for Sick Children","funders":"National Eye Institute","keywords":"Missense mutation; Biology; Kinesin; Proband; Genetics; Strabismus; Extraocular muscles; Mutation; Gene; Anatomy; Microtubule","score_opus":0.010438920009685514,"score_gpt":0.27123471406637445,"score_spread":0.26079579405668896,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2065581872","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99265844,0.00087649707,0.0013276251,0.00033674552,0.00015405354,0.000048111164,0.00068462134,0.00009312994,0.0038207332],"genre_scores_gemma":[0.9972506,0.00017883816,0.00066009467,0.00007742928,0.000065679604,0.000015985372,0.00017936253,0.000037741167,0.001534341],"study_design_codex":"case_report","study_design_gemma":"observational","domain_scores_codex":[0.9993469,0.00006669831,0.000090933085,0.00017627772,0.00017312176,0.0001461565],"domain_scores_gemma":[0.998946,0.00039395125,0.0003353283,0.000039132115,0.000056117817,0.00022950163],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0003466085,0.0019637314,0.0008192756,0.0017987535,0.001406576,0.0006320721,0.00074367947,0.002566481,0.005787653],"category_scores_gemma":[0.00181119,0.00052296254,0.0006966949,0.0008517072,0.0013120458,0.00055980403,0.0010567583,0.0009650371,0.00083817303],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0017965405,0.00039831814,0.033393774,0.0003035902,0.00032988493,0.59562063,0.0013891396,0.0009963373,0.33662978,0.003294396,0.0031332655,0.022714322],"study_design_scores_gemma":[0.00031546035,0.0009196368,0.106198855,0.000097379256,0.00044659537,0.8232409,0.0006182295,0.001994974,0.0590801,0.0012121234,0.005723286,0.00015240925],"about_ca_topic_score_codex":0.0032899538,"about_ca_topic_score_gemma":0.0036659457,"teacher_disagreement_score":0.005787653,"about_ca_system_score_codex":0.00045371262,"about_ca_system_score_gemma":0.00047979114,"threshold_uncertainty_score":0.019361615},"labels":[],"label_agreement":null},{"id":"W2065766094","doi":"10.1038/ng.2249","title":"Genome-wide meta-analysis identifies 56 bone mineral density loci and reveals 14 loci associated with risk of fracture","year":2012,"lang":"en","type":"review","venue":"Nature Genetics","topic":"Bone health and osteoporosis research","field":"Medicine","cited_by":1215,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Manitoba; Hôpital Saint-François d'Assise; Centre hospitalier universitaire de Québec; University of British Columbia; McGill University","funders":"National Center for Advancing Translational Sciences; National Institute of Arthritis and Musculoskeletal and Skin Diseases; National Institute of Neurological Disorders and Stroke; National Cancer Institute; National Human Genome Research Institute; National Heart, Lung, and Blood Institute; Instituto de Salud Carlos III; Health Research Council of New Zealand; Canadian Institutes of Health Research; Eli Lilly Canada; College of Pharmacy, University of Michigan; National Institutes of Health; Hjartavernd; Kulturministeriet; National Institute of Diabetes and Digestive and Kidney Diseases; Turun Yliopistollinen Keskussairaala; Syddansk Universitet; Göteborgs Läkaresällskap; Emil Aaltosen Säätiö; Vetenskapsrådet; Paavo Nurmen Säätiö; Amgen Canada; Centre for Medical Systems Biology; Novo Nordisk; Juho Vainion Säätiö; Healthway; Kempe Foundation; Versus Arthritis; Ministry of Agriculture, Forestry and Fisheries; National Center for Research Resources; National and Kapodistrian University of Athens; Bundesministerium für Verkehr, Innovation und Technologie; National Health and Medical Research Council; Jewish General Hospital; Suomen Kulttuurirahasto; Tampereen Tuberkuloosisäätiö; Kela; Medical Research Council; Servier; King's College London; Australian Cancer Research Foundation; Geelong Region Medical Research Foundation; University of Michigan; Fondation Leducq; Dairy Farmers of Canada; World Anti-Doping Agency; Steirische Wirtschaftsförderungsgesellschaft; National Institute for Health and Care Research; Cedars-Sinai Medical Center; Austrian Federal Ministry of Economy, Family and Youth; Nederlandse Organisatie voor Wetenschappelijk Onderzoek; Svenska Läkaresällskapet; Arthritis Society; Stiftelsen för Strategisk Forskning; National Institute on Aging; University of Hong Kong; British Heart Foundation; Scottish Government; Chronic Disease Research Foundation; Wellcome Trust; Procter and Gamble; Amgen; Pfizer; Donald W. Reynolds Foundation; Eli Lilly and Company; Erasmus Universitair Medisch Centrum Rotterdam; European Commission; Sanofi","keywords":"Genome-wide association study; Bone mineral; Biology; Osteoporosis; Bone density; Genetic association; Genetics; Internal medicine; Bioinformatics; Single-nucleotide polymorphism; Endocrinology; Gene; Medicine; Genotype","score_opus":0.05598249574234243,"score_gpt":0.360566883404893,"score_spread":0.3045843876625506,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2065766094","genre_codex":"review","genre_gemma":"review","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"review","genre_consensus":"review","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.0021150291,0.9961437,0.00056271587,0.0005768836,0.00011296033,0.0000053902536,0.00019357709,0.000016732254,0.00027303406],"genre_scores_gemma":[0.02173949,0.9751545,0.0013942355,0.0006725755,0.00028323414,0.000015207629,0.00045766827,0.000007751949,0.00027532142],"study_design_codex":"design_other","study_design_gemma":"meta_analysis","domain_scores_codex":[0.9995378,0.000113798495,0.00006831079,0.0001304608,0.00011914339,0.000030552193],"domain_scores_gemma":[0.99893147,0.0007386099,0.00013715043,0.000045443023,0.00010978816,0.00003748104],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0015236405,0.0015605608,0.0036512478,0.0017347018,0.00017520062,0.0007751605,0.001149698,0.00095014,0.0016291877],"category_scores_gemma":[0.0021984545,0.00042705337,0.002384119,0.002987271,0.0002580261,0.00041856282,0.000564605,0.0008870283,0.000310932],"study_design_candidate":"meta_analysis","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0015108755,0.00008556183,0.027102442,0.031613808,0.035207853,0.0010359496,0.000076259596,0.0008941377,0.0025669225,0.0010670223,0.017251698,0.88158745],"study_design_scores_gemma":[0.0020130633,0.0012892176,0.25792915,0.023519058,0.2517598,0.011797946,0.0004966465,0.0016956923,0.004153779,0.014620387,0.43028963,0.0004356888],"about_ca_topic_score_codex":0.0022831918,"about_ca_topic_score_gemma":0.007670123,"teacher_disagreement_score":0.0036512478,"about_ca_system_score_codex":0.00040394705,"about_ca_system_score_gemma":0.0011190957,"threshold_uncertainty_score":0.008057892},"labels":[],"label_agreement":null},{"id":"W2065796189","doi":"10.1038/ng1631","title":"Genomic alterations in cultured human embryonic stem cells","year":2005,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Pluripotent Stem Cells Research","field":"Biochemistry, Genetics and Molecular Biology","cited_by":622,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Robarts Clinical Trials","funders":"","keywords":"Biology; Embryonic stem cell; Epigenetics; Genetics; Mutant; Mutation; Phenotype; Cell culture; Gene; Stem cell; DNA methylation; Cell biology; Molecular biology; Gene expression","score_opus":0.010644632895779906,"score_gpt":0.2815304612595475,"score_spread":0.2708858283637676,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2065796189","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.980838,0.002336839,0.006956953,0.00027404484,0.00012670513,0.00006921818,0.003285251,0.00021360409,0.005899435],"genre_scores_gemma":[0.98975664,0.0011074978,0.002358441,0.00010273609,0.000016448357,0.000056301655,0.0029543387,0.00007339675,0.0035742966],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99978346,0.000045328754,0.000042217212,0.00004392911,0.00006348182,0.00002156929],"domain_scores_gemma":[0.9997247,0.00010909539,0.000037082667,0.00006624256,0.000041048414,0.000021955986],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00013358449,0.00015827194,0.00016677169,0.00044038016,0.00021728841,0.00037781885,0.00020489257,0.0002391755,0.0022746508],"category_scores_gemma":[0.00044560735,0.00020141953,0.00020113107,0.0003316392,0.00018956192,0.00018897287,0.00021123038,0.00042109593,0.0007062592],"study_design_candidate":"bench_or_experimental","study_design_consensus":"bench_or_experimental","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00006544833,0.0000138593305,0.0008045593,0.000029419076,0.000010938662,0.00024762045,0.000046089997,0.00019951165,0.99606556,0.00016176203,0.00009515333,0.0022601965],"study_design_scores_gemma":[0.000010626405,0.00010401396,0.018406587,0.0000073434335,0.00003982723,0.0006375226,0.000094694595,0.0005254515,0.97507304,0.00013925457,0.0049562273,0.0000054652387],"about_ca_topic_score_codex":0.0020002087,"about_ca_topic_score_gemma":0.0023649423,"teacher_disagreement_score":0.0022746508,"about_ca_system_score_codex":0.00028670533,"about_ca_system_score_gemma":0.00020463936,"threshold_uncertainty_score":0.0076094866},"labels":[],"label_agreement":null},{"id":"W2065890382","doi":"10.1038/ng.2270","title":"Detectable clonal mosaicism and its relationship to aging and cancer","year":2012,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Genomic variations and chromosomal abnormalities","field":"Biochemistry, Genetics and Molecular Biology","cited_by":594,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Mount Sinai Hospital; Public Health Ontario; University of Toronto; Lunenfeld-Tanenbaum Research Institute","funders":"National Cancer Institute; National Institutes of Health; Cancer Research UK","keywords":"Biology; Genetics; Cancer; Evolutionary biology","score_opus":0.010211925282419227,"score_gpt":0.25734040005568976,"score_spread":0.24712847477327052,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2065890382","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99262816,0.0030179932,0.0019839706,0.00018164793,0.000018917699,0.000009441064,0.00019410966,0.000052566756,0.0019132092],"genre_scores_gemma":[0.9987864,0.00041247442,0.00033000723,0.000017943148,0.00001620988,0.0000035889755,0.000044362143,0.0000045670213,0.00038460505],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9998839,0.000029507893,0.00001169487,0.000026557498,0.000030993095,0.000017326327],"domain_scores_gemma":[0.9993881,0.00025821826,0.00017391544,0.00006283818,0.00004021812,0.000076635304],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0002839072,0.00011918122,0.0001336752,0.0010596324,0.00016480831,0.0002147325,0.00021762823,0.00032985886,0.0014013267],"category_scores_gemma":[0.0009644373,0.00015401552,0.000103283186,0.0004042469,0.00035139488,0.00025024783,0.0002412498,0.00030694078,0.0000859813],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.001610924,0.00010567332,0.14914627,0.00009948927,0.00008639574,0.007283512,0.00029577521,0.0005520696,0.804864,0.006807445,0.0005292505,0.028619135],"study_design_scores_gemma":[0.000057648645,0.00091520644,0.8076181,0.000013729837,0.00012319942,0.04628278,0.00028318926,0.0027142672,0.1290053,0.0075162915,0.005422313,0.0000479823],"about_ca_topic_score_codex":0.000506769,"about_ca_topic_score_gemma":0.00044966725,"teacher_disagreement_score":0.0014013267,"about_ca_system_score_codex":0.00014877123,"about_ca_system_score_gemma":0.0001328324,"threshold_uncertainty_score":0.0046879053},"labels":[],"label_agreement":null},{"id":"W2066199795","doi":"10.1038/ng.1053","title":"Rare MTNR1B variants impairing melatonin receptor 1B function contribute to type 2 diabetes","year":2012,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Circadian rhythm and melatonin","field":"Neuroscience","cited_by":361,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"McGill University and Génome Québec Innovation Centre; McGill University; Centre Hospitalier de l’Université de Montréal; PROCURE","funders":"Agence Nationale de la Recherche; Wellcome Trust","keywords":"Minor allele frequency; Biology; Type 2 diabetes; Odds ratio; Nonsynonymous substitution; Genome-wide association study; Genetics; Genotyping; Allele; Internal medicine; Single-nucleotide polymorphism; Allele frequency; Endocrinology; Genotype; Diabetes mellitus; Gene; Medicine; Genome","score_opus":0.013514031424252407,"score_gpt":0.25049414519372687,"score_spread":0.23698011376947448,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2066199795","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.988283,0.0016598983,0.0048050247,0.0011374679,0.00033961615,0.00004272848,0.0007126427,0.00019452917,0.0028251472],"genre_scores_gemma":[0.99515545,0.00040529424,0.002400601,0.00032378614,0.0002603698,0.00002092502,0.00024943275,0.00011643168,0.0010676513],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.99917954,0.00017150285,0.00014430037,0.00026819104,0.00014979873,0.0000866962],"domain_scores_gemma":[0.9983687,0.00045964078,0.0007523253,0.00011777091,0.00008527405,0.00021641358],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0005317574,0.0019595816,0.00090592244,0.0010974819,0.0012034492,0.00087374187,0.0009870261,0.0025339648,0.0071807555],"category_scores_gemma":[0.0022222616,0.00054989755,0.0009352151,0.0009445156,0.0009413864,0.00042130717,0.0007095514,0.0016323739,0.00066995167],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.010205991,0.0006977492,0.13226062,0.00050595787,0.0022603292,0.13696511,0.0013932184,0.0021599396,0.6704353,0.007174366,0.004452992,0.031488404],"study_design_scores_gemma":[0.0018498575,0.0015034544,0.5498035,0.0005243897,0.0037849958,0.35022962,0.0010644427,0.00779438,0.053280275,0.011747558,0.018080445,0.00033701066],"about_ca_topic_score_codex":0.001978177,"about_ca_topic_score_gemma":0.0018823069,"teacher_disagreement_score":0.0071807555,"about_ca_system_score_codex":0.00036777306,"about_ca_system_score_gemma":0.000286037,"threshold_uncertainty_score":0.024021983},"labels":[],"label_agreement":null},{"id":"W2066293229","doi":"10.1038/ng.3162","title":"Gene-gene and gene-environment interactions detected by transcriptome sequence analysis in twins","year":2014,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Bioinformatics and Genomic Networks","field":"Biochemistry, Genetics and Molecular Biology","cited_by":244,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"McGill University","funders":"National Institute of Mental Health; Swiss Institute of Bioinformatics; Schweizerischer Nationalfonds zur Förderung der Wissenschaftlichen Forschung; Louis-Jeantet Foundation; Canadian Institutes of Health Research; National Institute for Health and Care Research; Wellcome Trust; King's College London; National Institutes of Health; National Science Foundation","keywords":"Biology; Genetics; Gene; Allele; Gene expression; Genetic architecture; Transcriptome; Regulation of gene expression; Pair-rule gene; Computational biology; Regulator gene; Quantitative trait locus","score_opus":0.005154320662816287,"score_gpt":0.22568196417608902,"score_spread":0.22052764351327273,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2066293229","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99915576,0.000044001914,0.00042661032,0.000016335985,0.0000032438063,0.0000019494667,0.00013536532,0.0000025532804,0.00021424472],"genre_scores_gemma":[0.99916136,0.00003434823,0.00045179293,0.000013593782,0.0000024947615,0.0000044673297,0.00015882748,0.0000053774984,0.00016767641],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9993299,0.00019556598,0.00004125535,0.00016258295,0.00013136605,0.00013933338],"domain_scores_gemma":[0.99888057,0.0004000226,0.00026326432,0.000100682024,0.00016338784,0.00019202649],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0005730311,0.00014574037,0.0003422,0.0009777686,0.00048460165,0.0006937542,0.00031531602,0.00035840488,0.00083698233],"category_scores_gemma":[0.0033169405,0.00020624542,0.00047786385,0.0007689964,0.00034927306,0.00020171511,0.0007023066,0.00037186602,0.00015028282],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.002139247,0.00013382758,0.71768695,0.0000702715,0.0005141145,0.0012662538,0.0014991275,0.0014883225,0.25891346,0.002074242,0.00025968178,0.013954574],"study_design_scores_gemma":[0.0000140566235,0.00011993018,0.9842138,0.000012655227,0.00017533828,0.00094202755,0.0008254661,0.0032292644,0.008362948,0.0016439911,0.00043964252,0.00002084919],"about_ca_topic_score_codex":0.00550151,"about_ca_topic_score_gemma":0.0067984173,"teacher_disagreement_score":0.00550151,"about_ca_system_score_codex":0.00034620374,"about_ca_system_score_gemma":0.00041945477,"threshold_uncertainty_score":0.010939002},"labels":[],"label_agreement":null},{"id":"W2066534789","doi":"10.1038/ng.777","title":"Mutations in origin recognition complex gene ORC4 cause Meier-Gorlin syndrome","year":2011,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Congenital limb and hand anomalies","field":"Biochemistry, Genetics and Molecular Biology","cited_by":171,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of British Columbia; Université de Montréal; Izaak Walton Killam Health Centre; Dalhousie University","funders":"Canadian Institutes of Health Research","keywords":"Biology; Genetics; Missense mutation; Gene; Germline mutation; Short stature; Genetic heterogeneity; Exon; Mutation; Phenotype","score_opus":0.04019459738193144,"score_gpt":0.2748864677330826,"score_spread":0.2346918703511512,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2066534789","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9914623,0.0016442218,0.002048286,0.000638601,0.00014650832,0.00003665315,0.0002939623,0.0002495687,0.003479963],"genre_scores_gemma":[0.99369437,0.00053422485,0.0031918162,0.00017736555,0.000108839624,0.00002079282,0.0001865278,0.00010412881,0.001981892],"study_design_codex":"case_report","study_design_gemma":"observational","domain_scores_codex":[0.9995709,0.00005309328,0.000050502822,0.00009879215,0.00014754463,0.00007915902],"domain_scores_gemma":[0.999203,0.0002654578,0.00030329102,0.000036971353,0.000032433116,0.00015891001],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0002149769,0.002976794,0.0011583704,0.0022358447,0.00066427863,0.00070521573,0.0011910705,0.0035399408,0.0045788735],"category_scores_gemma":[0.001021782,0.000774303,0.0007455709,0.0010915872,0.0014313926,0.0006535701,0.0011322487,0.0011955986,0.00079707697],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0013239156,0.00016024591,0.028950924,0.00033815866,0.00049177004,0.48393887,0.00057061197,0.0015260346,0.46476972,0.0040234155,0.001929048,0.011977249],"study_design_scores_gemma":[0.00073582894,0.0004136978,0.09420243,0.00010841642,0.0015429514,0.57118326,0.00065768015,0.007840008,0.2988562,0.004228492,0.019977452,0.00025352833],"about_ca_topic_score_codex":0.002593931,"about_ca_topic_score_gemma":0.0022445545,"teacher_disagreement_score":0.0045788735,"about_ca_system_score_codex":0.00074269646,"about_ca_system_score_gemma":0.00056982314,"threshold_uncertainty_score":0.015317798},"labels":[],"label_agreement":null},{"id":"W2067135122","doi":"10.1038/ng931","title":"Meiotic arrest and aneuploidy in MLH3-deficient mice","year":2002,"lang":"en","type":"article","venue":"Nature Genetics","topic":"DNA Repair Mechanisms","field":"Biochemistry, Genetics and Molecular Biology","cited_by":384,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"York University","funders":"","keywords":"Biology; Meiosis; Homologous chromosome; Genetics; Homologous recombination; Cell biology; DNA; Gene","score_opus":0.006431706652702413,"score_gpt":0.22340365181212574,"score_spread":0.21697194515942334,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2067135122","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.98216337,0.002579281,0.005257963,0.00074157474,0.0001296599,0.00010460468,0.0036800085,0.0009772314,0.0043664332],"genre_scores_gemma":[0.98252374,0.0017498706,0.0027922906,0.00024827482,0.0001031378,0.0001389725,0.0013037398,0.00047697235,0.0106629245],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9994103,0.00007284633,0.0000834911,0.00015819607,0.00016006298,0.00011519837],"domain_scores_gemma":[0.9983563,0.00026514937,0.00070637086,0.0001392522,0.000065702094,0.0004672978],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00040257676,0.001408181,0.0008743518,0.003923595,0.0006549862,0.0009126329,0.0009968859,0.0019692003,0.006349704],"category_scores_gemma":[0.00052426715,0.00092689344,0.00069568946,0.00077813014,0.0013622696,0.0006716192,0.00085138826,0.0025056433,0.0012300559],"study_design_candidate":"bench_or_experimental","study_design_consensus":"bench_or_experimental","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00074876583,0.00008379347,0.00052381237,0.000054381966,0.000024521063,0.0010274956,0.000042164113,0.00018309073,0.9950942,0.00079298404,0.00018121119,0.0012435503],"study_design_scores_gemma":[0.0004887113,0.00059817027,0.014355458,0.000065719054,0.000144449,0.008615111,0.0001247477,0.0017773793,0.9664648,0.0012310824,0.006079028,0.000055291457],"about_ca_topic_score_codex":0.0011254128,"about_ca_topic_score_gemma":0.0012628747,"teacher_disagreement_score":0.006349704,"about_ca_system_score_codex":0.0006857527,"about_ca_system_score_gemma":0.00044646958,"threshold_uncertainty_score":0.021241903},"labels":[],"label_agreement":null},{"id":"W2067406483","doi":"10.1038/ng.3217","title":"Common variants in ACYP2 influence susceptibility to cisplatin-induced hearing loss","year":2015,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Hearing, Cochlea, Tinnitus, Genetics","field":"Neuroscience","cited_by":132,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Hospital for Sick Children","funders":"National Institute of General Medical Sciences; National Institute on Deafness and Other Communication Disorders; National Cancer Institute","keywords":"Ototoxicity; Biology; Hearing loss; Cisplatin; Genetics; Hazard ratio; Genetic predisposition; Audiology; Genetic variation; Oncology; Internal medicine; Gene; Chemotherapy; Confidence interval; Medicine","score_opus":0.061981890091680765,"score_gpt":0.3434797453234621,"score_spread":0.28149785523178134,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2067406483","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99471384,0.0006156091,0.0014872829,0.0002993726,0.000056006353,0.000031733343,0.0008680255,0.00009395942,0.0018342161],"genre_scores_gemma":[0.99838054,0.00012384265,0.00046120898,0.00008023626,0.000025729396,0.000011352401,0.0002607173,0.00004873138,0.0006075367],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9992434,0.0001539823,0.000090571084,0.00024916354,0.00017895437,0.00008399222],"domain_scores_gemma":[0.998456,0.00062258274,0.00046551536,0.00012098137,0.00011700928,0.0002179595],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00037083635,0.0011746577,0.00056473765,0.0014211255,0.00056076876,0.0008266057,0.00069756195,0.0013767416,0.0077029774],"category_scores_gemma":[0.0022393898,0.00037339705,0.0010110221,0.0013528572,0.00058244047,0.00039325212,0.0007010534,0.00080632104,0.0006597303],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.009179766,0.0004220065,0.47729194,0.00035451984,0.002814849,0.019371767,0.0009075241,0.0026564128,0.45832083,0.0022732946,0.0030099233,0.023397198],"study_design_scores_gemma":[0.00032652248,0.0006328397,0.93497115,0.00012510279,0.0016220924,0.021110235,0.00040013963,0.0047893072,0.028204892,0.0023914014,0.0053056898,0.00012063465],"about_ca_topic_score_codex":0.0029565447,"about_ca_topic_score_gemma":0.0022394205,"teacher_disagreement_score":0.0077029774,"about_ca_system_score_codex":0.0003225638,"about_ca_system_score_gemma":0.0003247481,"threshold_uncertainty_score":0.025768995},"labels":[],"label_agreement":null},{"id":"W2067941152","doi":"10.1038/86966","title":"Characterizing gene expression profile of Inv(16)-associated leukemia","year":2001,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Acute Myeloid Leukemia Research","field":"Medicine","cited_by":0,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Abbott (Canada)","funders":"","keywords":"Biology; Genetics; Leukemia; Gene expression; Gene; Computational biology; Expression (computer science); Cancer research","score_opus":0.016925075790903677,"score_gpt":0.29740863356572106,"score_spread":0.28048355777481737,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2067941152","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9977927,0.00031035545,0.00060806994,0.000022103779,0.000006138056,0.0000073405768,0.0005706966,0.000016157996,0.000666336],"genre_scores_gemma":[0.9938421,0.0004935832,0.0013593591,0.000041439453,0.000011587557,0.000022997932,0.0020838238,0.000017594863,0.0021274074],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99990785,0.000007384604,0.000005430711,0.00002306801,0.000020683456,0.000035500532],"domain_scores_gemma":[0.9999373,0.000011942933,0.000017141167,0.0000053067956,0.000011320063,0.000016903316],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00007108112,0.00012742338,0.0001779824,0.0005144594,0.0001562086,0.0002771301,0.000086345375,0.00014475081,0.0012874876],"category_scores_gemma":[0.0001323916,0.000092882234,0.00013212612,0.0004382638,0.00012605138,0.00010101987,0.00015240345,0.00022343767,0.00038588126],"study_design_candidate":"bench_or_experimental","study_design_consensus":"bench_or_experimental","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00034326967,0.000018310326,0.009184599,0.000015869511,0.0000060201073,0.00011551642,0.000030321753,0.000049679154,0.9878478,0.000051547173,0.000050023355,0.0022870605],"study_design_scores_gemma":[0.000044135726,0.00072409306,0.4510187,0.000010920401,0.00009649566,0.0036812075,0.0004717505,0.002258449,0.5344001,0.0003592342,0.0069195163,0.000015434463],"about_ca_topic_score_codex":0.0004643321,"about_ca_topic_score_gemma":0.0007137036,"teacher_disagreement_score":0.0012874876,"about_ca_system_score_codex":0.00014582406,"about_ca_system_score_gemma":0.00010731742,"threshold_uncertainty_score":0.0043070912},"labels":[],"label_agreement":null},{"id":"W2068114378","doi":"10.1038/ng1096","title":"Chromosome 6q25 is linked to susceptibility to leprosy in a Vietnamese population","year":2003,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Leprosy Research and Treatment","field":"Medicine","cited_by":190,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"McGill University Health Centre; McGill University; McGill Genome Centre","funders":"","keywords":"Leprosy; Mycobacterium leprae; Biology; Genetics; Allele; Vietnamese; Genetic linkage; Microsatellite; Disease; Population; Immunology; Gene; Internal medicine; Medicine","score_opus":0.017339523641999158,"score_gpt":0.3408571721382853,"score_spread":0.32351764849628617,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2068114378","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99926454,0.00010378801,0.00010181026,0.00008144317,0.000005673005,0.000008186159,0.000090674985,0.000002612828,0.0003411141],"genre_scores_gemma":[0.99855405,0.00012623757,0.00016095789,0.000047280846,0.000010101861,0.000008414983,0.000103293714,0.000003610304,0.0009859703],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9997017,0.0000763045,0.000024287094,0.000096827695,0.000035076795,0.0000657757],"domain_scores_gemma":[0.9996581,0.000081592036,0.00008595396,0.000016929276,0.00004738456,0.00011008146],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0003048995,0.0006384578,0.00038974726,0.0011564454,0.0011933123,0.00045619564,0.0005244896,0.00042204995,0.00364191],"category_scores_gemma":[0.0007994396,0.00033192543,0.00038854883,0.0010627173,0.00053365645,0.00017730317,0.00037482224,0.00047042398,0.0002716605],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0018829327,0.00057991943,0.86950153,0.00013735387,0.00046522173,0.047735073,0.013128904,0.0004957968,0.048363507,0.00087916,0.0010729053,0.015757788],"study_design_scores_gemma":[0.00010736871,0.0006017451,0.98051286,0.000040494775,0.00020115706,0.012057453,0.0031816685,0.0004462975,0.00089374103,0.00026644126,0.0016679106,0.00002278179],"about_ca_topic_score_codex":0.042286552,"about_ca_topic_score_gemma":0.023394108,"teacher_disagreement_score":0.042286552,"about_ca_system_score_codex":0.00044270078,"about_ca_system_score_gemma":0.00043424455,"threshold_uncertainty_score":0.084080815},"labels":[],"label_agreement":null},{"id":"W2068162513","doi":"10.1038/ng.2238","title":"Common variants at 12q15 and 12q24 are associated with infant head circumference","year":2012,"lang":"en","type":"review","venue":"Nature Genetics","topic":"Genetic Associations and Epidemiology","field":"Biochemistry, Genetics and Molecular Biology","cited_by":143,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Lunenfeld-Tanenbaum Research Institute; Ontario Institute for Cancer Research; University of Toronto; Mount Sinai Hospital","funders":"National Institute of Mental Health; National Heart, Lung, and Blood Institute; Biocenter, University of Oulu; Helmholtz Zentrum München; Instituto de Salud Carlos III; National Health and Medical Research Council; Medical Research Council; Canadian Institutes of Health Research; National Institute for Health and Care Research; Gentofte Hospital; Weill Cornell Medical College; Nederlandse Organisatie voor Wetenschappelijk Onderzoek; Centers for Disease Control and Prevention; University of Toronto; Oulun Yliopisto; Statens Serum Institut; University of Bristol; Nierstichting; Universitair Medisch Centrum Groningen; Erasmus Universiteit Rotterdam; National Institutes of Health; Rijksuniversiteit Groningen; Eunice Kennedy Shriver National Institute of Child Health and Human Development; ZonMw; University of Exeter; Raine Medical Research Foundation; Erasmus Medisch Centrum; British Heart Foundation; Wellcome Trust; School of Public Health, Imperial College London; Fundació la Marató de TV3; Imperial College London; Children's Hospital of Philadelphia; Helsingin Yliopisto","keywords":"Genome-wide association study; Biology; Head circumference; Single-nucleotide polymorphism; Genetics; Circumference; Genetic association; Chromosome; Pregnancy; Genotype; Birth weight; Gene","score_opus":0.03248821434197286,"score_gpt":0.3195655284947759,"score_spread":0.287077314152803,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2068162513","genre_codex":"review","genre_gemma":"review","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"review","genre_consensus":"review","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.00086215633,0.99667656,0.0005612481,0.0007061642,0.00018691496,0.0000042579295,0.000106252075,0.000016199336,0.0008801675],"genre_scores_gemma":[0.0038857178,0.9938378,0.00079504953,0.00025036233,0.0004241771,0.0000091368065,0.00013761404,0.0000042238235,0.0006559331],"study_design_codex":"design_other","study_design_gemma":"observational","domain_scores_codex":[0.99972016,0.000051689694,0.00004327015,0.000075532516,0.00008962543,0.000019734223],"domain_scores_gemma":[0.9993622,0.00036970663,0.00011337784,0.000017572456,0.00010695179,0.000030109224],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0006789846,0.0010342356,0.0012992071,0.0016271693,0.00015959858,0.0006566347,0.0009680096,0.0008690514,0.0021061613],"category_scores_gemma":[0.0015910283,0.0002874542,0.00048716055,0.001957005,0.0005333046,0.00052283244,0.0005529934,0.0010190542,0.0006458499],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00017907984,0.000031509848,0.0058207815,0.005614595,0.0003575195,0.00085913367,0.0000433255,0.0004195971,0.001063108,0.0015937773,0.0213643,0.9626533],"study_design_scores_gemma":[0.000117017764,0.00011733299,0.0493935,0.009193461,0.0020278883,0.01550277,0.00024010437,0.00048049277,0.0015903877,0.008285932,0.9129455,0.000105561274],"about_ca_topic_score_codex":0.0034232636,"about_ca_topic_score_gemma":0.004750191,"teacher_disagreement_score":0.0034232636,"about_ca_system_score_codex":0.00043070383,"about_ca_system_score_gemma":0.00078721764,"threshold_uncertainty_score":0.0070458055},"labels":[],"label_agreement":null},{"id":"W2068388603","doi":"10.1038/ng.523","title":"Meta-analysis of genome-wide association data identifies a risk locus for major mood disorders on 3p21.1","year":2010,"lang":"en","type":"review","venue":"Nature Genetics","topic":"Genetic Associations and Epidemiology","field":"Biochemistry, Genetics and Molecular Biology","cited_by":186,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Centre for Addiction and Mental Health; University of Toronto","funders":"U.S. National Library of Medicine; National Institute of Mental Health; Alfried Krupp von Bohlen und Halbach-Stiftung; National Institutes of Health; Schweizerischer Nationalfonds zur Förderung der Wissenschaftlichen Forschung; Universität Heidelberg; Deutsche Forschungsgemeinschaft; GlaxoSmithKline; National Alliance for Research on Schizophrenia and Depression; Chinese Society of Clinical Oncology; National Human Genome Research Institute; Wellcome Trust; Foundation for the National Institutes of Health; National Science Foundation","keywords":"Genome-wide association study; Major depressive disorder; Mood disorders; Bipolar disorder; Odds ratio; Single-nucleotide polymorphism; Genetic association; Biology; SNP; Meta-analysis; Mood; Locus (genetics); Genetics; Genotype; Psychiatry; Psychology; Internal medicine; Medicine; Gene","score_opus":0.04763945570915269,"score_gpt":0.34916282212606425,"score_spread":0.3015233664169116,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2068388603","genre_codex":"review","genre_gemma":"review","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"review","genre_consensus":"review","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.0004230549,0.9969693,0.0008366528,0.0010219888,0.00019833981,0.000006095654,0.00014816341,0.000020591679,0.00037594553],"genre_scores_gemma":[0.004340574,0.99288636,0.0011971897,0.0005665515,0.00044019768,0.000016640808,0.0002807925,0.000008081901,0.00026354377],"study_design_codex":"design_other","study_design_gemma":"meta_analysis","domain_scores_codex":[0.9991549,0.0002495438,0.000100372265,0.00022584257,0.00023131515,0.00003800959],"domain_scores_gemma":[0.99600923,0.0029171123,0.00036300774,0.00012584132,0.0004626771,0.000122133],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0034523732,0.0015018142,0.0041515254,0.0022165575,0.00019297253,0.0011162024,0.0019229952,0.0012730228,0.0023644452],"category_scores_gemma":[0.004401103,0.0004555768,0.0016728146,0.0033433405,0.0004220162,0.00058385136,0.0006486372,0.001530318,0.00093342236],"study_design_candidate":"meta_analysis","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00069792254,0.000039757026,0.0060614827,0.015553174,0.006433474,0.0005981564,0.000032739994,0.0006630349,0.0011481049,0.0015909491,0.02945553,0.93772566],"study_design_scores_gemma":[0.0009632761,0.0007459446,0.07484241,0.023169573,0.034804314,0.012470832,0.00021641131,0.0015185406,0.003618121,0.02030979,0.8270786,0.00026220654],"about_ca_topic_score_codex":0.0025484846,"about_ca_topic_score_gemma":0.005112601,"teacher_disagreement_score":0.0041515254,"about_ca_system_score_codex":0.0007669031,"about_ca_system_score_gemma":0.0016543185,"threshold_uncertainty_score":0.018258154},"labels":[],"label_agreement":null},{"id":"W2069777680","doi":"10.1038/ng.2477","title":"New loci associated with birth weight identify genetic links between intrauterine growth and adult height and metabolism","year":2012,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Birth, Development, and Health","field":"Medicine","cited_by":320,"is_retracted":false,"has_abstract":false,"route_ca_aff":false,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"","funders":"National Institute of Child Health and Human Development; National Institute of Environmental Health Sciences; National Institute of Allergy and Infectious Diseases; National Human Genome Research Institute; National Heart, Lung, and Blood Institute; Biomedical Research Council; Strategic Research Council; European Regional Development Fund; Instituto de Salud Carlos III; National Center for Research Resources; Centers for Disease Control and Prevention; Fogarty International Center; National Institutes of Health; Norwegian Biodiversity Information Centre; Versus Arthritis; U.S. Public Health Service; Novo Nordisk Foundation Center for Basic Metabolic Research; H. Lundbeck A/S; University of Bristol; Egmont Fonden; National Institute of Diabetes and Digestive and Kidney Diseases; Turun Yliopistollinen Keskussairaala; Chinese Society of Clinical Oncology; National Institute of Mental Health; Danmarks Grundforskningsfond; Syddansk Universitet; Augustinus Fonden; Emil Aaltosen Säätiö; Paavo Nurmen Säätiö; Centre for Medical Systems Biology; Novo Nordisk; Juho Vainion Säätiö; Lundbeckfonden; Generalitat de Catalunya; Generalitat Valenciana; Deutsche Forschungsgemeinschaft; Nederlandse Organisatie voor Wetenschappelijk Onderzoek; Turun Yliopistosäätiö; Erasmus Medisch Centrum; Vrije Universiteit Amsterdam; Erasmus Universiteit Rotterdam; ZonMw; Münchner Zentrum für Gesundheitswissenschaften; Curtin University of Technology; National Health and Medical Research Council; Oulun Yliopisto; Schweizerischer Nationalfonds zur Förderung der Wissenschaftlichen Forschung; National Science Foundation; Boehringer Ingelheim Fonds; Raine Medical Research Foundation; Sundhed og Sygdom, Det Frie Forskningsråd; Ministerio de Ciencia e Innovación; European Commission; Biocenter, University of Oulu; National Research Foundation; National Institute for Health and Care Research; Canadian Institutes of Health Research; Diabetes UK; University of Southampton; Cancer Research UK; Wellcome Trust; British Heart Foundation; Women and Infants Research Foundation; Children's Hospital of Philadelphia; Medical Research Council; Fundació la Marató de TV3; Yrjö Jahnssonin Säätiö; Juvenile Diabetes Research Foundation International; March of Dimes Foundation; Tampereen Tuberkuloosisäätiö; Universität Potsdam; Eunice Kennedy Shriver National Institute of Child Health and Human Development; GlaxoSmithKline; Scottish Government","keywords":"Biology; Genome-wide association study; Genetics; Birth weight; Type 2 diabetes; Genetic association; Phenotype; Diabetes mellitus; Physiology; Gene; Single-nucleotide polymorphism; Pregnancy; Endocrinology; Genotype","score_opus":0.01021468824782447,"score_gpt":0.26722907765869547,"score_spread":0.257014389410871,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2069777680","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99223524,0.0013661688,0.0040982785,0.0003916389,0.00006851493,0.00001197979,0.00040432776,0.000065748434,0.0013581498],"genre_scores_gemma":[0.9923003,0.0006739524,0.0052882717,0.00012878502,0.00009462194,0.000019153305,0.00028214938,0.000053912252,0.0011587513],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9995565,0.00010128831,0.000034866734,0.0001234372,0.0001211414,0.00006266145],"domain_scores_gemma":[0.997692,0.001279702,0.0005786995,0.00014000374,0.00009573539,0.00021381193],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0006409055,0.0009596774,0.0004888857,0.0021770368,0.00036078657,0.0006771148,0.0007061764,0.0009937751,0.0038147513],"category_scores_gemma":[0.0019361564,0.00056117616,0.0007372237,0.0013174308,0.00053542445,0.000258031,0.00067690195,0.00093480264,0.00028701877],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0064388695,0.00048051486,0.52316207,0.00022650731,0.0016855365,0.0062552877,0.0013367546,0.0022589155,0.40316537,0.005851469,0.0012392611,0.04789941],"study_design_scores_gemma":[0.00023709169,0.0002720085,0.9715927,0.000061858744,0.0006662483,0.0034068883,0.00023518517,0.0027805658,0.014403314,0.0043656295,0.001916924,0.00006149711],"about_ca_topic_score_codex":0.0016643942,"about_ca_topic_score_gemma":0.0026901748,"teacher_disagreement_score":0.0038147513,"about_ca_system_score_codex":0.00023500851,"about_ca_system_score_gemma":0.00020790212,"threshold_uncertainty_score":0.0127616525},"labels":[],"label_agreement":null},{"id":"W2070595030","doi":"10.1038/ng1249","title":"Loss of collagenase-2 confers increased skin tumor susceptibility to male mice","year":2003,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Protease and Inhibitor Mechanisms","field":"Biochemistry, Genetics and Molecular Biology","cited_by":532,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of British Columbia","funders":"","keywords":"Biology; Matrix metalloproteinase; Tumor progression; Cancer research; Collagenase; Cancer; Immunology; Internal medicine; Genetics; Medicine; Enzyme","score_opus":0.00544375035677575,"score_gpt":0.2380422700173854,"score_spread":0.23259851966060965,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2070595030","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99090344,0.0008088307,0.003929969,0.00019247284,0.00007331422,0.000037283535,0.0013246877,0.00043910366,0.0022907562],"genre_scores_gemma":[0.9866044,0.0006739105,0.0018656519,0.000084128056,0.000053595842,0.000053615528,0.00093203236,0.00028808572,0.009444522],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9992586,0.00012640559,0.00006706925,0.00016793086,0.0002322036,0.0001478997],"domain_scores_gemma":[0.9986437,0.0001908552,0.00054948445,0.00013069026,0.000052159936,0.00043310682],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00027149142,0.0011097103,0.00050646527,0.0024989424,0.00036720687,0.0006236613,0.00050777546,0.0007456537,0.006418769],"category_scores_gemma":[0.00026866593,0.00070715393,0.0006275977,0.0005694393,0.00053827977,0.0003690928,0.0006288436,0.0016149922,0.0015303028],"study_design_candidate":"bench_or_experimental","study_design_consensus":"bench_or_experimental","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00019663766,0.000046148547,0.00032542832,0.000009739549,0.000007684906,0.00009790793,0.000012909058,0.000029919122,0.9986777,0.00009041714,0.000032557247,0.0004729263],"study_design_scores_gemma":[0.00003750815,0.0003678082,0.011142477,0.000008951934,0.000038747203,0.0012105805,0.000046624347,0.00038936434,0.9855402,0.00006809431,0.0011349177,0.000014672484],"about_ca_topic_score_codex":0.0009210513,"about_ca_topic_score_gemma":0.001662921,"teacher_disagreement_score":0.006418769,"about_ca_system_score_codex":0.0005538603,"about_ca_system_score_gemma":0.0002832213,"threshold_uncertainty_score":0.02147293},"labels":[],"label_agreement":null},{"id":"W2071390670","doi":"10.1038/ng1352","title":"The Bardet-Biedl protein BBS4 targets cargo to the pericentriolar region and is required for microtubule anchoring and cell cycle progression","year":2004,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Genetic and Kidney Cyst Diseases","field":"Biochemistry, Genetics and Molecular Biology","cited_by":396,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Simon Fraser University","funders":"Canadian Institutes of Health Research; National Cancer Institute; March of Dimes Foundation; National Institutes of Health; Michael Smith Health Research BC; Wellcome Trust; Heart and Stroke Foundation of Canada","keywords":"Cell biology; Centrosome; Biology; Microtubule; Cilium; Genetics; Cell cycle; Cell","score_opus":0.00428589089783333,"score_gpt":0.23927376298870132,"score_spread":0.234987872090868,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2071390670","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9802889,0.004217056,0.009576786,0.0007465303,0.00021181609,0.000019923564,0.0009305254,0.0004072273,0.0036011238],"genre_scores_gemma":[0.98666084,0.0006175934,0.0035011566,0.00009669348,0.000019011879,0.0000131949655,0.0014855561,0.00007554766,0.007530425],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9998118,0.000024500268,0.000015757403,0.000041035237,0.00006449411,0.000042489602],"domain_scores_gemma":[0.99978095,0.000019248255,0.00006799355,0.00002242095,0.000035854762,0.00007357446],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00017901842,0.00034049523,0.00021822417,0.00045125364,0.00061628013,0.0006644207,0.0003543882,0.00051703164,0.0021448836],"category_scores_gemma":[0.00028025132,0.0003848765,0.00022688237,0.00021633603,0.00037668512,0.0004095015,0.00057987915,0.00067669293,0.0018213972],"study_design_candidate":"bench_or_experimental","study_design_consensus":"bench_or_experimental","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0001318284,0.000007889363,0.0003864063,0.000023474106,0.000005783822,0.000075625394,0.000005163697,0.00008974727,0.99783283,0.00028646772,0.00019011679,0.0009646238],"study_design_scores_gemma":[0.000020290052,0.00003007238,0.008394425,0.000004213716,0.000009640491,0.000394966,0.000020691936,0.0017459082,0.983697,0.0001618637,0.005512832,0.00000821077],"about_ca_topic_score_codex":0.0012841503,"about_ca_topic_score_gemma":0.0018568389,"teacher_disagreement_score":0.0021448836,"about_ca_system_score_codex":0.0012410589,"about_ca_system_score_gemma":0.00035074493,"threshold_uncertainty_score":0.009004533},"labels":[],"label_agreement":null},{"id":"W2071882769","doi":"10.1038/ng0110-9","title":"Reply to “Evolutionary flux of canonical microRNAs and mirtrons in Drosophila”","year":2009,"lang":"en","type":"article","venue":"Nature Genetics","topic":"MicroRNA in disease regulation","field":"Biochemistry, Genetics and Molecular Biology","cited_by":10,"is_retracted":false,"has_abstract":false,"route_ca_aff":false,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"","funders":"National Institute of General Medical Sciences; National Institutes of Health; European Commission; Canada's Michael Smith Genome Sciences Centre; V Foundation for Cancer Research","keywords":"Biology; microRNA; Gene; Genetics; myr; Drosophila (subgenus); DNA sequencing; RNA; Evolutionary biology; Oligonucleotide; Computational biology; Genome","score_opus":0.005000632156968833,"score_gpt":0.25238770363194424,"score_spread":0.2473870714749754,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2071882769","genre_codex":"commentary","genre_gemma":"commentary","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"commentary","genre_consensus":"commentary","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.0005244949,0.0030554826,0.00039232327,0.9226051,0.0727354,0.000008145956,0.00011748979,0.000048286183,0.0005133777],"genre_scores_gemma":[0.004398329,0.0021934025,0.00040951275,0.9239658,0.06527529,0.000030966272,0.000077620425,0.000036084042,0.0036129153],"study_design_codex":"not_applicable","study_design_gemma":"not_applicable","domain_scores_codex":[0.99824595,0.00036192962,0.0002778604,0.00037089575,0.00045242757,0.00029092844],"domain_scores_gemma":[0.99038774,0.004823412,0.00073017715,0.0003816819,0.0024308665,0.0012461678],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.004393154,0.0010538906,0.0014411117,0.00090007094,0.002909532,0.002892359,0.0026173873,0.024074467,0.0046195616],"category_scores_gemma":[0.019276194,0.00095621287,0.0013291946,0.0008640313,0.0036777104,0.0036459125,0.0025336985,0.035147384,0.0036050808],"study_design_candidate":"not_applicable","study_design_consensus":"not_applicable","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00014690796,0.000022325257,0.0004642693,0.00011444804,0.000050324754,0.00039296635,0.00016507274,0.00011139998,0.0005965476,0.002474224,0.990387,0.0050745513],"study_design_scores_gemma":[0.00016914091,0.000082096056,0.0029113367,0.00024350344,0.00010611797,0.0009203038,0.0005871221,0.00053752924,0.0015545146,0.0088736955,0.98389006,0.00012458734],"about_ca_topic_score_codex":0.0026554528,"about_ca_topic_score_gemma":0.0036876516,"teacher_disagreement_score":0.024074467,"about_ca_system_score_codex":0.002284161,"about_ca_system_score_gemma":0.002289286,"threshold_uncertainty_score":0.023233533},"labels":[],"label_agreement":null},{"id":"W2072043914","doi":"10.1038/ng.419","title":"Genetic variants at 6p21.33 are associated with susceptibility to follicular lymphoma","year":2009,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Chronic Lymphocytic Leukemia Research","field":"Medicine","cited_by":156,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Canada's Michael Smith Genome Sciences Centre; BC Cancer Agency","funders":"National Institute of Environmental Health Sciences; National Cancer Institute; National Heart, Lung, and Blood Institute","keywords":"Follicular lymphoma; Chronic lymphocytic leukemia; Lymphoma; Biology; Follicular phase; Allele; Genetic association; Genome-wide association study; Leukemia; Genetics; Single-nucleotide polymorphism; Immunology; Gene; Genotype","score_opus":0.01167607600136909,"score_gpt":0.2837860582958836,"score_spread":0.2721099822945145,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2072043914","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9971878,0.0006687093,0.00041664197,0.00027940105,0.000022559825,0.00001158696,0.0002817993,0.00003601888,0.0010955923],"genre_scores_gemma":[0.9987872,0.00021590122,0.00029449386,0.00003736051,0.000050646773,0.0000065946665,0.00016178151,0.0000108314525,0.00043532462],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9996227,0.00012960749,0.00003705039,0.000071702714,0.00008227502,0.00005666064],"domain_scores_gemma":[0.9986688,0.0005094543,0.0005225752,0.000073455405,0.000072759314,0.00015295688],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00035674116,0.0007096617,0.00029951325,0.0014111948,0.00041355437,0.00040695717,0.00047374074,0.001008346,0.0061665075],"category_scores_gemma":[0.0026942552,0.00029982894,0.00036555986,0.0013888003,0.0004005788,0.00021948977,0.0003132489,0.00070299394,0.00062485103],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0079719825,0.00032145323,0.75376225,0.00025954508,0.00080678874,0.023962542,0.0010749329,0.0013630936,0.16757724,0.0017878355,0.0040142816,0.03709804],"study_design_scores_gemma":[0.00026570758,0.0004894064,0.9582795,0.000067347864,0.00045062287,0.027529657,0.00025827833,0.0012178392,0.005921177,0.002093261,0.0033891303,0.000037996568],"about_ca_topic_score_codex":0.001586496,"about_ca_topic_score_gemma":0.0011566262,"teacher_disagreement_score":0.0061665075,"about_ca_system_score_codex":0.00018652753,"about_ca_system_score_gemma":0.00011715304,"threshold_uncertainty_score":0.020629048},"labels":[],"label_agreement":null},{"id":"W2072441383","doi":"10.1038/ng.2925","title":"Recurrent activating ACVR1 mutations in diffuse intrinsic pontine glioma","year":2014,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Heterotopic Ossification and Related Conditions","field":"Medicine","cited_by":525,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"BC Cancer Agency","funders":"National Institute of Neurological Disorders and Stroke; Rosetrees Trust; Brain Tumour Charity; Canadian Institutes of Health Research; Cancer Research UK; Wellcome Trust","keywords":"Biology; Fibrodysplasia ossificans progressiva; Mutation; Cancer research; Germline; Germline mutation; Cancer; Somatic cell; Internal medicine; Bioinformatics; Gene; Genetics; Medicine; Heterotopic ossification","score_opus":0.012422609475823838,"score_gpt":0.29721037270677825,"score_spread":0.2847877632309544,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2072441383","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9961046,0.00037753995,0.00034641725,0.0001321561,0.000014797258,0.000013023797,0.000118449825,0.00003953616,0.0028534802],"genre_scores_gemma":[0.99947995,0.000067914756,0.00014901298,0.000013800194,0.000011650246,0.0000014110321,0.00003465202,0.000006514661,0.00023525425],"study_design_codex":"case_report","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.999652,0.000024151672,0.000038627586,0.0000681212,0.00012054424,0.00009650908],"domain_scores_gemma":[0.999424,0.00012922384,0.00021226151,0.000054466185,0.00004755825,0.00013245265],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00016707856,0.0005440012,0.00037965734,0.001169693,0.0004007144,0.00059504,0.00072927464,0.0012526178,0.002086856],"category_scores_gemma":[0.0011748162,0.00024824383,0.00034422745,0.00085293315,0.00072667625,0.0003783871,0.00053110655,0.0005289143,0.00042068647],"study_design_candidate":"bench_or_experimental","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0005656853,0.0000796792,0.0710155,0.00013471776,0.00010767752,0.7939448,0.0007411322,0.0014961625,0.110773735,0.0014468544,0.00077904254,0.018914962],"study_design_scores_gemma":[0.00005920664,0.00021650031,0.095278956,0.000020991965,0.00015990702,0.8836854,0.00043008605,0.0021274444,0.014946837,0.0008760644,0.0021518818,0.000046804784],"about_ca_topic_score_codex":0.0032177763,"about_ca_topic_score_gemma":0.004469596,"teacher_disagreement_score":0.0032177763,"about_ca_system_score_codex":0.0006546261,"about_ca_system_score_gemma":0.0004519198,"threshold_uncertainty_score":0.006981194},"labels":[],"label_agreement":null},{"id":"W2072881647","doi":"10.1038/ng.3002","title":"Rare variants of large effect in BRCA2 and CHEK2 affect risk of lung cancer","year":2014,"lang":"en","type":"article","venue":"Nature Genetics","topic":"BRCA gene mutations in cancer","field":"Biochemistry, Genetics and Molecular Biology","cited_by":481,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Princess Margaret Cancer Centre; University Health Network; Lunenfeld-Tanenbaum Research Institute; Mount Sinai Hospital","funders":"National Institute of General Medical Sciences; National Institute on Drug Abuse; National Cancer Institute; Cancer Research UK; National Institutes of Health; National Heart, Lung, and Blood Institute; National Institute for Health and Care Research; National Human Genome Research Institute; World Health Organization","keywords":"CHEK2; Genome-wide association study; Lung cancer; Biology; Odds ratio; Imputation (statistics); Genetic association; 1000 Genomes Project; Haplotype; Adenocarcinoma; Genetics; Case-control study; Lung cancer susceptibility; Oncology; Cancer; Genotype; Internal medicine; Single-nucleotide polymorphism; Medicine; Gene; Germline mutation; Mutation","score_opus":0.002728455304103668,"score_gpt":0.279527572723023,"score_spread":0.2767991174189193,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2072881647","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9913756,0.0019582182,0.0024598516,0.00039820207,0.00009431917,0.000026761687,0.001082568,0.0001971465,0.0024073096],"genre_scores_gemma":[0.9981566,0.00016181216,0.0006860827,0.00008332944,0.0000686737,0.000007939557,0.00020297304,0.000043089814,0.00058944325],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99902403,0.00027445803,0.00010506427,0.00028943794,0.00021457204,0.00009237257],"domain_scores_gemma":[0.9974866,0.0014404684,0.0005501511,0.00016193441,0.000102189704,0.00025863777],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0006184004,0.0014038854,0.0009141027,0.0020506168,0.00064419315,0.0006582679,0.00079598627,0.0021265137,0.005947691],"category_scores_gemma":[0.003673469,0.0005554058,0.0010745217,0.0012295072,0.000799821,0.0004160469,0.0007057471,0.0009053417,0.000557639],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0078688,0.00032238627,0.5948013,0.0002590985,0.0028662272,0.053131685,0.00079287204,0.003501885,0.30508202,0.002989089,0.0028125776,0.0255721],"study_design_scores_gemma":[0.00037785675,0.00046995445,0.9208527,0.000083602165,0.0015015354,0.046723098,0.00028693624,0.0036512953,0.020043984,0.0025761316,0.0033196725,0.00011328732],"about_ca_topic_score_codex":0.0030550112,"about_ca_topic_score_gemma":0.0031370777,"teacher_disagreement_score":0.005947691,"about_ca_system_score_codex":0.00031199533,"about_ca_system_score_gemma":0.00019508954,"threshold_uncertainty_score":0.019896984},"labels":[],"label_agreement":null},{"id":"W2073167340","doi":"10.1038/ng.200","title":"Genetic variants near TNFAIP3 on 6q23 are associated with systemic lupus erythematosus","year":2008,"lang":"en","type":"article","venue":"Nature Genetics","topic":"NF-κB Signaling Pathways","field":"Biochemistry, Genetics and Molecular Biology","cited_by":582,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Université de Montréal; Arthritis Research Centre of Canada; Montreal Heart Institute; Toronto Western Hospital; University of Toronto; University Health Network","funders":"National Institute of Allergy and Infectious Diseases; National Institute of Arthritis and Musculoskeletal and Skin Diseases; National Institute of Mental Health; Wellcome Trust","keywords":"Rheumatoid arthritis; Genome-wide association study; Genetic association; Immunology; Autoimmune disease; Allele; Biology; Disease; Genetics; Lupus erythematosus; Internal medicine; Medicine; Single-nucleotide polymorphism; Genotype; Gene; Antibody","score_opus":0.008836452152573277,"score_gpt":0.2152684915429251,"score_spread":0.20643203939035182,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2073167340","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9952839,0.0011727907,0.0011845019,0.0004505666,0.0000981226,0.0000201603,0.00053446816,0.000091311114,0.0011641401],"genre_scores_gemma":[0.997863,0.00021600774,0.00078781205,0.000105694664,0.00012397149,0.000010662136,0.00017140401,0.000024511162,0.00069689925],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.99923515,0.0001938082,0.00010507025,0.00019109357,0.00019742333,0.00007756672],"domain_scores_gemma":[0.9979651,0.000539777,0.0010265523,0.00008362502,0.00010366876,0.0002813718],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0004398549,0.0018176594,0.00088526186,0.001999161,0.0009411339,0.0006968022,0.0009843488,0.002149974,0.0063173063],"category_scores_gemma":[0.002145011,0.00046636522,0.0009585859,0.0020115068,0.000649122,0.00031517717,0.0004226874,0.0012879119,0.0008231813],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.011959921,0.0006641522,0.3233503,0.00045998074,0.0028698505,0.13630927,0.0011841555,0.0019571462,0.49211437,0.001670862,0.0032068177,0.024253216],"study_design_scores_gemma":[0.0007455605,0.0011825119,0.7637745,0.00016147975,0.0022038845,0.19358522,0.00052654813,0.0026804549,0.027149081,0.002336032,0.0054884274,0.00016625713],"about_ca_topic_score_codex":0.0015274872,"about_ca_topic_score_gemma":0.001536188,"teacher_disagreement_score":0.0063173063,"about_ca_system_score_codex":0.00031581032,"about_ca_system_score_gemma":0.00021539851,"threshold_uncertainty_score":0.021133542},"labels":[],"label_agreement":null},{"id":"W2073582448","doi":"10.1038/ng.301","title":"Genome-wide association study for early-onset and morbid adult obesity identifies three new risk loci in European populations","year":2009,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Genetic Associations and Epidemiology","field":"Biochemistry, Genetics and Molecular Biology","cited_by":654,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"McGill University and Génome Québec Innovation Centre","funders":"","keywords":"Biology; Genome-wide association study; Genetics; Obesity; Genetic association; Association (psychology); Evolutionary biology; Single-nucleotide polymorphism; Gene; Genotype; Endocrinology","score_opus":0.012411541934080384,"score_gpt":0.2761257143579682,"score_spread":0.2637141724238878,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2073582448","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9984199,0.00033652026,0.000589044,0.00008214131,0.000009741614,0.0000056733365,0.00010750716,0.000009799563,0.0004396194],"genre_scores_gemma":[0.99901545,0.00009888389,0.0005036875,0.00003924857,0.00000959377,0.000005244784,0.000093115086,0.000006257711,0.00022859183],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99922204,0.00024412102,0.000088992216,0.00022324451,0.00010486686,0.00011680404],"domain_scores_gemma":[0.99812764,0.000701881,0.00043830177,0.00022507181,0.00016654067,0.00034048804],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0016173664,0.0006329679,0.00053402205,0.000995949,0.0006402294,0.00086807733,0.0007812436,0.0010668122,0.0017911],"category_scores_gemma":[0.0026888356,0.0003896685,0.0008484287,0.0011573314,0.000744733,0.00032873845,0.0008464403,0.0010734188,0.00016234507],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0024520638,0.0001501264,0.9791821,0.000022093189,0.00051690306,0.0007915105,0.00039942143,0.00009916487,0.011700261,0.0003286963,0.00013800304,0.0042195944],"study_design_scores_gemma":[0.000053948268,0.000095144605,0.9980166,0.0000061868654,0.00018552138,0.00067561766,0.00011427243,0.00014138916,0.00039612898,0.00019183554,0.00011710634,0.0000064441665],"about_ca_topic_score_codex":0.0034478714,"about_ca_topic_score_gemma":0.0032985215,"teacher_disagreement_score":0.0034478714,"about_ca_system_score_codex":0.00021084788,"about_ca_system_score_gemma":0.00029566127,"threshold_uncertainty_score":0.008553565},"labels":[],"label_agreement":null},{"id":"W2074576256","doi":"10.1038/ng0108-8","title":"BRCA1—sowing the seeds crooked in the furrow","year":2007,"lang":"en","type":"article","venue":"Nature Genetics","topic":"PI3K/AKT/mTOR signaling in cancer","field":"Biochemistry, Genetics and Molecular Biology","cited_by":11,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"McGill University","funders":"","keywords":"Biology; PTEN; Aneuploidy; Mutation; Sowing; Genetics; Cancer research; Chromosome; Gene; Horticulture; Signal transduction","score_opus":0.008333333219562098,"score_gpt":0.2828294399270495,"score_spread":0.2744961067074874,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2074576256","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9481128,0.0037519094,0.017144926,0.005499485,0.0012749974,0.00022662694,0.0027814659,0.0033196216,0.017888017],"genre_scores_gemma":[0.94036955,0.001123184,0.0154726375,0.0011394785,0.000055245466,0.00007775591,0.0010835426,0.00046479952,0.040213782],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99985766,0.000010369122,0.000007973166,0.00004902113,0.000039869523,0.00003518335],"domain_scores_gemma":[0.9997812,0.000021400838,0.00006062683,0.000033738343,0.000013610648,0.000089429224],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00013609511,0.00034292694,0.00038885136,0.00037504476,0.00041394384,0.00037107506,0.00053162646,0.0008420784,0.005494752],"category_scores_gemma":[0.00019796588,0.00039421002,0.0003038751,0.00014047262,0.00050526485,0.00032035323,0.00032480166,0.0016784839,0.0018435882],"study_design_candidate":"bench_or_experimental","study_design_consensus":"bench_or_experimental","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00029950525,0.00005290677,0.0002857659,0.000033815217,0.000007815829,0.00015879018,0.00000960448,0.000114583425,0.99260217,0.0006703039,0.0010514274,0.004713315],"study_design_scores_gemma":[0.00005262945,0.00025182037,0.003601343,0.000013466106,0.000012030715,0.00075029116,0.00003291219,0.0009193479,0.9817524,0.00032623616,0.012273987,0.000013561449],"about_ca_topic_score_codex":0.0023788544,"about_ca_topic_score_gemma":0.004242677,"teacher_disagreement_score":0.005494752,"about_ca_system_score_codex":0.0007529552,"about_ca_system_score_gemma":0.00060169824,"threshold_uncertainty_score":0.018381774},"labels":[],"label_agreement":null},{"id":"W2074656730","doi":"10.1038/ng.2870","title":"Pancreatic islet enhancer clusters enriched in type 2 diabetes risk-associated variants","year":2014,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Pancreatic function and diabetes","field":"Medicine","cited_by":553,"is_retracted":false,"has_abstract":false,"route_ca_aff":false,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"","funders":"Institute of Genetics; Medical Research Council; Eli Lilly and Company; European Foundation for the Study of Diabetes; Ministerio de Economía y Competitividad; Biomedical Research Council; National Medical Research Council; National Research Foundation; National University of Singapore; National Institute for Health and Care Research; Vanderbilt University; Wellcome Trust; Harvard University; Johns Hopkins University","keywords":"Enhancer; Biology; Islet; Epigenome; Genetics; Chromatin; Transcription factor; Pancreatic islets; Type 2 diabetes; DNA methylation; Gene; Diabetes mellitus; Endocrinology; Gene expression","score_opus":0.006499235824400895,"score_gpt":0.24571770496270892,"score_spread":0.23921846913830802,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2074656730","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.98757684,0.0013886831,0.004240375,0.00019212897,0.00007542672,0.000022690272,0.0035581135,0.00015671346,0.0027890278],"genre_scores_gemma":[0.99371535,0.00020461278,0.0019044682,0.00017628398,0.00003143781,0.00002033587,0.002326051,0.00008643375,0.0015349998],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9993175,0.000082802246,0.000046440404,0.00030495206,0.00010943757,0.00013883848],"domain_scores_gemma":[0.99912935,0.00040541348,0.00016939187,0.00009792138,0.000060374925,0.00013760843],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00040165082,0.0003610625,0.00058259396,0.0012495916,0.0006318213,0.00069038157,0.00048859057,0.0005660178,0.010194032],"category_scores_gemma":[0.0011720782,0.00035711785,0.0009594182,0.0012675746,0.0003442319,0.0002292692,0.0006927272,0.00078425254,0.0008531717],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.006881608,0.000211502,0.4757033,0.0004887692,0.0029096936,0.0045017893,0.0012555362,0.0022187582,0.46081334,0.003550225,0.004565035,0.036900487],"study_design_scores_gemma":[0.00034782515,0.00022667296,0.95970416,0.00010506726,0.0015768005,0.0059859185,0.00043495788,0.0020599342,0.017270705,0.002549209,0.009670715,0.0000679882],"about_ca_topic_score_codex":0.0037958256,"about_ca_topic_score_gemma":0.006735346,"teacher_disagreement_score":0.010194032,"about_ca_system_score_codex":0.00020055886,"about_ca_system_score_gemma":0.0003133896,"threshold_uncertainty_score":0.03410244},"labels":[],"label_agreement":null},{"id":"W2075183916","doi":"10.1038/ng.2811","title":"Genomic analyses identify distinct patterns of selection in domesticated pigs and Tibetan wild boars","year":2013,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Cancer-related molecular mechanisms research","field":"Biochemistry, Genetics and Molecular Biology","cited_by":583,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Alberta","funders":"","keywords":"Wild boar; Biology; Domestication; Genetic diversity; Genome; Genetics; Population; Whole genome sequencing; Evolutionary biology; Gene; Ecology","score_opus":0.01129854555533553,"score_gpt":0.3200080480091169,"score_spread":0.30870950245378137,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2075183916","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9993461,0.00013614517,0.00017188498,0.000011628108,0.0000022016357,0.0000016923709,0.0000918336,0.0000028240083,0.00023578356],"genre_scores_gemma":[0.99862695,0.00010357194,0.00025976024,0.000046610126,0.000005431736,0.00000693253,0.0003605527,0.000008775098,0.0005814252],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99978,0.000056176024,0.000011334148,0.00007112953,0.000025534155,0.00005588086],"domain_scores_gemma":[0.99970716,0.00010597102,0.0000763751,0.000020366955,0.000027122796,0.00006285297],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00031967837,0.00024120312,0.0002794626,0.0013127765,0.0002904451,0.00045440276,0.0003137723,0.00026704633,0.0016467551],"category_scores_gemma":[0.0002915101,0.00020063327,0.0003220144,0.00084526674,0.0005468294,0.0001403414,0.00034296536,0.00033949787,0.00016395799],"study_design_candidate":"bench_or_experimental","study_design_consensus":"bench_or_experimental","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0014788416,0.00008265813,0.25263196,0.000089579546,0.00031744354,0.00060133036,0.0010095317,0.00014554373,0.734689,0.00035646136,0.00009404541,0.008503551],"study_design_scores_gemma":[0.000009144792,0.00010425723,0.9970988,0.0000046765012,0.00003147592,0.00021141254,0.0002578352,0.000096266805,0.0019895565,0.00004718606,0.00014578585,0.0000037226016],"about_ca_topic_score_codex":0.0017228255,"about_ca_topic_score_gemma":0.0042335046,"teacher_disagreement_score":0.0017228255,"about_ca_system_score_codex":0.00021829721,"about_ca_system_score_gemma":0.00012918981,"threshold_uncertainty_score":0.0055089593},"labels":[],"label_agreement":null},{"id":"W2075396092","doi":"10.1038/ng.489","title":"Common variants at five new loci associated with early-onset inflammatory bowel disease","year":2009,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Inflammatory Bowel Disease","field":"Biochemistry, Genetics and Molecular Biology","cited_by":484,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Mount Sinai Hospital; SickKids Foundation; Hospital for Sick Children; University of Toronto","funders":"National Center for Research Resources; Crohn's and Colitis Foundation of Canada; National Institute of Diabetes and Digestive and Kidney Diseases; Canadian Institutes of Health Research; Medical Research Council; Children's Hospital of Philadelphia; Canadian Child Health Clinician Scientist Program; National Institutes of Health; Action Medical Research; Canadian Association of Gastroenterology; Scottish Government; Wellcome Trust","keywords":"Ulcerative colitis; Inflammatory bowel disease; Age of onset; Disease; Crohn's disease; Genome-wide association study; Biology; Etiology; Colitis; Immunology; Internal medicine; Medicine; Genetics; Gene; Single-nucleotide polymorphism; Genotype","score_opus":0.003830444674962622,"score_gpt":0.22270115198494547,"score_spread":0.21887070730998284,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2075396092","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99481994,0.00075709436,0.0015153653,0.00018578838,0.00008761338,0.00003784728,0.00044652424,0.000048576898,0.0021013517],"genre_scores_gemma":[0.99762017,0.00014758638,0.0011586818,0.000087995584,0.000084653344,0.00000835191,0.00026008757,0.000019352272,0.0006131054],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.998928,0.00017334156,0.00016403402,0.00024677673,0.0003092494,0.00017867915],"domain_scores_gemma":[0.99705255,0.0010720768,0.0009037212,0.00015042383,0.0002834912,0.00053773297],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0005546385,0.0016755596,0.0011525052,0.002987319,0.0009037792,0.0010032194,0.0012296799,0.001759791,0.004550948],"category_scores_gemma":[0.0027164498,0.00042655904,0.0012887353,0.001927928,0.00086581724,0.00032729833,0.00074858527,0.0011346196,0.00052028464],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.009496121,0.0007985443,0.5439805,0.0004160031,0.0016829026,0.21356149,0.0020390416,0.0012357272,0.2031269,0.002543368,0.0013765874,0.019742887],"study_design_scores_gemma":[0.00052444864,0.00069306104,0.8973202,0.00012022754,0.0013308212,0.08308444,0.00048502162,0.0010681106,0.011015243,0.0009206968,0.0033379013,0.0000998551],"about_ca_topic_score_codex":0.003105363,"about_ca_topic_score_gemma":0.0033917606,"teacher_disagreement_score":0.004550948,"about_ca_system_score_codex":0.00047673853,"about_ca_system_score_gemma":0.00034640616,"threshold_uncertainty_score":0.015224397},"labels":[],"label_agreement":null},{"id":"W2075458118","doi":"10.1038/ng.3113","title":"Mutations in SGOL1 cause a novel cohesinopathy affecting heart and gut rhythm","year":2014,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Skin and Cellular Biology Research","field":"Biochemistry, Genetics and Molecular Biology","cited_by":156,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Centre Hospitalier de l’Université de Montréal; Université du Québec à Chicoutimi; Canada's Michael Smith Genome Sciences Centre; Centre hospitalier universitaire de Québec; BC Cancer Agency; Centre Hospitalier Universitaire Sainte-Justine; Université de Montréal","funders":"Canadian Institutes of Health Research; CHU Sainte-Justine Foundation; Université de Montréal; University of Toronto; Nederlandse Organisatie voor Wetenschappelijk Onderzoek; ZonMw; Fondation Leducq; Fondation du Grand défi Pierre Lavoie; Ontario Genomics Institute; Génome Québec; Genome British Columbia; University of Ottawa; McGill University; Ontario Genomics; Genome Canada","keywords":"Biology; Zebrafish; Cohesin; Pathological; Cell biology; Endocrinology; Internal medicine; Genetics; Chromosome; Medicine","score_opus":0.010535137912140136,"score_gpt":0.28677960583791995,"score_spread":0.27624446792577984,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2075458118","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9937179,0.00068085146,0.0022415859,0.00052717194,0.0002062242,0.00006459304,0.00060526107,0.00021907047,0.001737286],"genre_scores_gemma":[0.997136,0.00016387113,0.0011546693,0.00013955844,0.00006878193,0.000015040492,0.0002528765,0.000053355117,0.0010158822],"study_design_codex":"case_report","study_design_gemma":"observational","domain_scores_codex":[0.99971324,0.000035873807,0.000046562855,0.00007574031,0.000073111485,0.000055476776],"domain_scores_gemma":[0.9987472,0.0004390834,0.00039523217,0.000047879792,0.000050067698,0.00032040532],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00020269878,0.00269143,0.0007439949,0.0013822096,0.0008393632,0.0006038524,0.0009600432,0.0025936684,0.00278521],"category_scores_gemma":[0.001081435,0.00048276182,0.0009324129,0.00081707665,0.0015317285,0.00028764553,0.0012185159,0.0010693688,0.0006649062],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0011361403,0.00017386867,0.018606633,0.00021658951,0.00033261342,0.5106663,0.000868193,0.0013037061,0.45369253,0.0017111425,0.0014690302,0.0098232245],"study_design_scores_gemma":[0.001075464,0.0014453515,0.16441287,0.00024648718,0.0012019874,0.62549424,0.001221578,0.008410476,0.17731673,0.0025333175,0.016290845,0.0003506568],"about_ca_topic_score_codex":0.0018695688,"about_ca_topic_score_gemma":0.00270899,"teacher_disagreement_score":0.00278521,"about_ca_system_score_codex":0.00060386333,"about_ca_system_score_gemma":0.00036128185,"threshold_uncertainty_score":0.009317458},"labels":[],"label_agreement":null},{"id":"W2076225138","doi":"10.1038/ng1604","title":"Variants of ENPP1 are associated with childhood and adult obesity and increase the risk of glucose intolerance and type 2 diabetes","year":2005,"lang":"en","type":"article","venue":"Nature Genetics","topic":"RNA modifications and cancer","field":"Biochemistry, Genetics and Molecular Biology","cited_by":321,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Université Laval","funders":"National Institute of Diabetes and Digestive and Kidney Diseases; National Institutes of Health","keywords":"Haplotype; Insulin resistance; Type 2 diabetes; Obesity; Childhood obesity; Biology; Internal medicine; Endocrinology; Allele; Locus (genetics); Genetics; Genotype; Odds ratio; Diabetes mellitus; Metabolic syndrome; Gene; Medicine; Overweight","score_opus":0.002194610444817037,"score_gpt":0.19589594869589413,"score_spread":0.1937013382510771,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2076225138","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9955064,0.0010828737,0.0015158103,0.00026468665,0.000040195857,0.0000075257954,0.0005142519,0.000048054768,0.0010201292],"genre_scores_gemma":[0.9969607,0.000477877,0.0010914933,0.00006404371,0.00005212609,0.0000084870635,0.00027341908,0.00002394826,0.0010477412],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99959415,0.0001197974,0.000040488205,0.00012291606,0.000082352904,0.00004026046],"domain_scores_gemma":[0.9986463,0.00045571732,0.00058958767,0.000080658385,0.00006239613,0.0001653012],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00039897094,0.001016092,0.00054173556,0.0007424665,0.0004837045,0.00053575373,0.0004581563,0.0010697024,0.004189962],"category_scores_gemma":[0.0014159462,0.0005365898,0.00039286914,0.0011244237,0.00043089522,0.00034587175,0.0003900625,0.0012513727,0.00030291767],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.009464705,0.0003097473,0.79818183,0.0002982449,0.0015653793,0.0148072755,0.00085416046,0.0019394706,0.14172086,0.002274258,0.0017851068,0.026798906],"study_design_scores_gemma":[0.00013091232,0.00028806934,0.96301687,0.000056436285,0.00055962504,0.021191763,0.00015046462,0.0015765445,0.009274852,0.0012553177,0.0024664525,0.00003263591],"about_ca_topic_score_codex":0.0016250955,"about_ca_topic_score_gemma":0.0013563269,"teacher_disagreement_score":0.004189962,"about_ca_system_score_codex":0.00018354133,"about_ca_system_score_gemma":0.00014099383,"threshold_uncertainty_score":0.014016867},"labels":[],"label_agreement":null},{"id":"W2076375535","doi":"10.1038/ng.2723","title":"Mutations in the gene encoding PDGF-B cause brain calcifications in humans and mice","year":2013,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Caveolin-1 and cellular processes","field":"Biochemistry, Genetics and Molecular Biology","cited_by":328,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Toronto","funders":"Schweizerischer Nationalfonds zur Förderung der Wissenschaftlichen Forschung","keywords":"PDGFB; PDGFRB; Biology; Missense mutation; Pericyte; PDGFRA; Calcification; Genetics; Platelet-derived growth factor receptor; Cancer research; Mutation; Gene; Pathology; Receptor; Growth factor; Stromal cell; Medicine","score_opus":0.01031861016336204,"score_gpt":0.2704553183096113,"score_spread":0.26013670814624923,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2076375535","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9874951,0.0023375766,0.0061704284,0.00033442158,0.00008093265,0.00003427172,0.0010495796,0.00032332182,0.0021743192],"genre_scores_gemma":[0.9937564,0.0013386385,0.0028993273,0.00012376097,0.000045841112,0.000026711714,0.0005123975,0.000109423534,0.001187535],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9996456,0.000044094628,0.000049536746,0.00011555287,0.000102951424,0.000042197666],"domain_scores_gemma":[0.99959534,0.000106464315,0.00016085383,0.000035975507,0.00002093831,0.00008035182],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0002517656,0.0012708639,0.0005777472,0.0020485206,0.0005238114,0.0004988651,0.00040712557,0.0015031713,0.0024181504],"category_scores_gemma":[0.00055574684,0.00073934393,0.00046178192,0.0006008954,0.0011463495,0.0002592581,0.00066423265,0.00090561516,0.0003957598],"study_design_candidate":"bench_or_experimental","study_design_consensus":"bench_or_experimental","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0015998984,0.000101475096,0.008084307,0.00016588475,0.00024039469,0.01889132,0.00034699184,0.00043615847,0.9575748,0.0015144624,0.0007211404,0.0103230635],"study_design_scores_gemma":[0.0011588425,0.0013400173,0.3202604,0.00032043373,0.0015521792,0.26646385,0.0010633824,0.005475627,0.37465274,0.007901047,0.01956086,0.00025070272],"about_ca_topic_score_codex":0.0024025205,"about_ca_topic_score_gemma":0.0019300928,"teacher_disagreement_score":0.0024181504,"about_ca_system_score_codex":0.00025473256,"about_ca_system_score_gemma":0.0003084345,"threshold_uncertainty_score":0.008089542},"labels":[],"label_agreement":null},{"id":"W2076446941","doi":"10.1038/ng.2599","title":"Mutations in DEPDC5 cause familial focal epilepsy with variable foci","year":2013,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Epilepsy research and treatment","field":"Medicine","cited_by":364,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Montreal Neurological Institute and Hospital; Centre Hospitalier de l’Université de Montréal; McGill University","funders":"","keywords":"Epilepsy; Biology; Exome sequencing; Epilepsy syndromes; Mutation; Etiology; Exome; Genetics; Neuroscience; Pathology; Gene; Medicine","score_opus":0.01234139198215136,"score_gpt":0.289955485727716,"score_spread":0.27761409374556467,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2076446941","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9808157,0.0031955463,0.0037088967,0.0009936685,0.00019110335,0.000041004478,0.0012398795,0.00011262277,0.00970167],"genre_scores_gemma":[0.998066,0.00019157883,0.0006513015,0.00013457841,0.000025393036,0.000004089346,0.00018348052,0.000016992955,0.000726647],"study_design_codex":"case_report","study_design_gemma":"observational","domain_scores_codex":[0.99980766,0.000022078062,0.00003398684,0.000050362254,0.000049606002,0.000036378427],"domain_scores_gemma":[0.9996413,0.00012063391,0.00010143572,0.000021804652,0.000025136042,0.000089726454],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00016080304,0.001158334,0.00034941046,0.0007226704,0.00044682046,0.0003857108,0.00046573664,0.0012753893,0.0034892426],"category_scores_gemma":[0.00060096954,0.0002236474,0.00043638019,0.00066754123,0.0008211648,0.00026444375,0.0006523728,0.00046210006,0.0004441582],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0015782492,0.00017543446,0.08029696,0.0004229065,0.00068191934,0.56212187,0.0006330287,0.0027634902,0.30313176,0.004684726,0.005154287,0.0383553],"study_design_scores_gemma":[0.0004458542,0.00035654273,0.15008348,0.00017734214,0.0005604077,0.72584915,0.00074319355,0.0038874806,0.09437636,0.0032381725,0.02016672,0.00011532787],"about_ca_topic_score_codex":0.0023188165,"about_ca_topic_score_gemma":0.0055698506,"teacher_disagreement_score":0.0034892426,"about_ca_system_score_codex":0.0006004434,"about_ca_system_score_gemma":0.0003082437,"threshold_uncertainty_score":0.011672735},"labels":[],"label_agreement":null},{"id":"W2076690763","doi":"10.1038/ng1845","title":"Mutations in the gene encoding the 3′-5′ DNA exonuclease TREX1 cause Aicardi-Goutières syndrome at the AGS1 locus","year":2006,"lang":"en","type":"article","venue":"Nature Genetics","topic":"interferon and immune responses","field":"Immunology and Microbiology","cited_by":892,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Centre Hospitalier Universitaire Sainte-Justine; Montreal Neurological Institute and Hospital","funders":"Medical Research Council; University of California, Santa Cruz","keywords":"Biology; Exonuclease; Phenotype; Gene; Innate immune system; Genetics; Locus (genetics); Loss function; Immune system; Polymerase","score_opus":0.00892631937471452,"score_gpt":0.2432654752861646,"score_spread":0.23433915591145008,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2076690763","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99587196,0.00045625193,0.0015716451,0.00034862303,0.000048774713,0.000017428052,0.00020791093,0.00020668443,0.0012706522],"genre_scores_gemma":[0.9975496,0.0001903721,0.0010906747,0.00006814097,0.00004893251,0.000008530356,0.000101878635,0.000035108398,0.000906854],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.99979347,0.000038874616,0.000021869262,0.000056320492,0.00006213626,0.000027499062],"domain_scores_gemma":[0.99921846,0.00037247207,0.00022830839,0.000035703804,0.000020419959,0.00012459974],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00013326578,0.0014808218,0.0005573624,0.0012069737,0.0005232388,0.00032557672,0.00036773132,0.0019097968,0.002681409],"category_scores_gemma":[0.00078596955,0.00034662633,0.0004813204,0.00048068448,0.0009495911,0.00025806128,0.00034810396,0.0011792841,0.00065165287],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.001295903,0.00015294952,0.024910958,0.00018041237,0.00016334426,0.16238026,0.0007205891,0.0017874911,0.7890908,0.0019625225,0.0014431359,0.01591165],"study_design_scores_gemma":[0.00044163244,0.0005990378,0.2100082,0.000096844145,0.00035524898,0.4687962,0.00037717982,0.0063795224,0.30411413,0.0024718125,0.0062267957,0.00013342804],"about_ca_topic_score_codex":0.0011213832,"about_ca_topic_score_gemma":0.0010945576,"teacher_disagreement_score":0.002681409,"about_ca_system_score_codex":0.00040440477,"about_ca_system_score_gemma":0.00019092108,"threshold_uncertainty_score":0.008970201},"labels":[],"label_agreement":null},{"id":"W2076811314","doi":"10.1038/ng.251","title":"Genetic variation in the KIF1B locus influences susceptibility to multiple sclerosis","year":2008,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Multiple Sclerosis Research Studies","field":"Medicine","cited_by":193,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of British Columbia","funders":"","keywords":"Locus (genetics); Biology; Multiple sclerosis; Genetics; Gene; Immunology","score_opus":0.06192096065158097,"score_gpt":0.31908928505923406,"score_spread":0.2571683244076531,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2076811314","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9982274,0.0005725911,0.00020377823,0.00013369761,0.000010704262,0.000003827285,0.000080640166,0.000007499467,0.00075996364],"genre_scores_gemma":[0.99916387,0.00015174552,0.00021292918,0.000029019973,0.000010600756,0.0000035466117,0.00006643517,0.000011272549,0.00035070968],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9986326,0.00069285685,0.000078564066,0.00027620865,0.00015416153,0.00016558672],"domain_scores_gemma":[0.9972805,0.0014732924,0.00064185064,0.00018459858,0.00016292834,0.00025691453],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.001310232,0.0005205076,0.00041587438,0.0021660393,0.0007263546,0.0006000572,0.0005594173,0.0007594375,0.0044697635],"category_scores_gemma":[0.0051681064,0.0003553021,0.00045619239,0.0015945232,0.00074608764,0.00041940034,0.00054763636,0.00071238895,0.00034714173],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0034145813,0.00022932036,0.93912065,0.00007292801,0.0008166199,0.0010507269,0.0011511157,0.00018516812,0.041565556,0.0005819792,0.0004076662,0.011403754],"study_design_scores_gemma":[0.00007997505,0.00019275724,0.99524313,0.00003296672,0.0002811907,0.0009591004,0.0003386055,0.00025233312,0.0016817308,0.00035971293,0.0005653565,0.0000131162315],"about_ca_topic_score_codex":0.009603336,"about_ca_topic_score_gemma":0.0058870073,"teacher_disagreement_score":0.009603336,"about_ca_system_score_codex":0.00046680935,"about_ca_system_score_gemma":0.00039183852,"threshold_uncertainty_score":0.019094825},"labels":[],"label_agreement":null},{"id":"W2076964189","doi":"10.1038/ng.2970","title":"ACVR1 mutations and the genomic landscape of pediatric diffuse glioma","year":2014,"lang":"en","type":"letter","venue":"Nature Genetics","topic":"Glioma Diagnosis and Treatment","field":"Medicine","cited_by":22,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Toronto","funders":"","keywords":"Glioma; Biology; Gene; Bioinformatics; Genetics","score_opus":0.008350025135256725,"score_gpt":0.24595032123563504,"score_spread":0.2376002961003783,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2076964189","genre_codex":"commentary","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":null,"domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.12006691,0.013610931,0.0017328641,0.83169246,0.0074112625,0.00005239528,0.0003249709,0.00021654452,0.024891745],"genre_scores_gemma":[0.74681985,0.011108248,0.0027561272,0.17741263,0.053749204,0.00006465343,0.00020604648,0.000091330774,0.0077919248],"study_design_codex":"case_report","study_design_gemma":"observational","domain_scores_codex":[0.99934775,0.0001880933,0.00006792676,0.00010044057,0.00017146075,0.00012434684],"domain_scores_gemma":[0.9981419,0.0010729684,0.00017768635,0.00008060019,0.00025249936,0.0002743507],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00055313413,0.0004241291,0.00078876596,0.0006775299,0.0009015842,0.0011177213,0.00085783494,0.00913654,0.00184999],"category_scores_gemma":[0.0058853915,0.00041724838,0.0005472132,0.0006301948,0.0010703906,0.001224319,0.00050735456,0.005706643,0.0006992342],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00065549545,0.00017994168,0.07251932,0.00027909837,0.00015507684,0.50139236,0.0006589524,0.0028435066,0.0059439912,0.012865894,0.32624003,0.076266326],"study_design_scores_gemma":[0.00034256026,0.0004536405,0.035251707,0.000419178,0.000259334,0.77951497,0.0011545928,0.010535466,0.0039024467,0.022250043,0.14578906,0.00012685747],"about_ca_topic_score_codex":0.0030211248,"about_ca_topic_score_gemma":0.0032530804,"teacher_disagreement_score":0.00913654,"about_ca_system_score_codex":0.0019150387,"about_ca_system_score_gemma":0.00082848687,"threshold_uncertainty_score":0.013894618},"labels":[],"label_agreement":null},{"id":"W2077016335","doi":"10.1038/ng.279","title":"Recurrent reciprocal 1q21.1 deletions and duplications associated with microcephaly or macrocephaly and developmental and behavioral abnormalities","year":2008,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Genomic variations and chromosomal abnormalities","field":"Biochemistry, Genetics and Molecular Biology","cited_by":635,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"North York General Hospital; Children's Hospital of Eastern Ontario","funders":"National Heart, Lung, and Blood Institute","keywords":"Macrocephaly; Microcephaly; Biology; Penetrance; Genetics; Proband; Non-allelic homologous recombination; Copy-number variation; Speech delay; Locus (genetics); Comparative genomic hybridization; Developmental disorder; Phenotype; Chromosome; Autism; Gene; Genome; Medicine; Mutation","score_opus":0.014482331268871952,"score_gpt":0.24841815495726546,"score_spread":0.23393582368839352,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2077016335","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9936512,0.000813245,0.0012817375,0.000355284,0.000046516976,0.000024737114,0.00089052634,0.00015668772,0.0027799613],"genre_scores_gemma":[0.9962353,0.0002425405,0.00081826746,0.00010092606,0.00006822529,0.000015849584,0.0005584414,0.000045487857,0.0019149991],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9994523,0.000040019302,0.00004437199,0.0001999397,0.00013811354,0.0001253302],"domain_scores_gemma":[0.9993191,0.00011217175,0.00032800765,0.000058283196,0.000035802772,0.00014671689],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00020388661,0.0016087061,0.0007459888,0.0012672112,0.0005224347,0.00056187226,0.00076850934,0.0013239798,0.0043382216],"category_scores_gemma":[0.0011673332,0.00044998454,0.0005093764,0.0009579605,0.0012486224,0.00028747888,0.0009417632,0.00078373856,0.0012795049],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0022444208,0.0003613708,0.036473546,0.00023235302,0.00033257494,0.20101963,0.0007783576,0.0017107667,0.7238612,0.0044696997,0.003459578,0.025056535],"study_design_scores_gemma":[0.00033579586,0.00066361204,0.21221238,0.000046725796,0.0005943227,0.70186096,0.0004575442,0.0013627933,0.071799845,0.0024665974,0.008056549,0.00014283822],"about_ca_topic_score_codex":0.0018712903,"about_ca_topic_score_gemma":0.003079457,"teacher_disagreement_score":0.0043382216,"about_ca_system_score_codex":0.00054770085,"about_ca_system_score_gemma":0.00045075297,"threshold_uncertainty_score":0.014512837},"labels":[],"label_agreement":null},{"id":"W2077735774","doi":"10.1038/ng.703","title":"The developmental dynamics of the maize leaf transcriptome","year":2010,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Genomics and Phylogenetic Studies","field":"Biochemistry, Genetics and Molecular Biology","cited_by":814,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Toronto","funders":"National Science Foundation","keywords":"Biology; Transcriptome; Gene; Computational biology; Alternative splicing; Genetics; Gene expression; Messenger RNA","score_opus":0.0038422058992161295,"score_gpt":0.21323595004519227,"score_spread":0.20939374414597614,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2077735774","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9888827,0.0018961175,0.004001573,0.00040560847,0.000015638978,0.000008816965,0.0011842956,0.000070280264,0.0035350416],"genre_scores_gemma":[0.9932219,0.0007960742,0.0010485415,0.00016090152,0.000021788243,0.000017099554,0.0012384076,0.000049689155,0.0034456376],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9998801,0.000010404301,0.0000049663204,0.000047473528,0.000030201922,0.000026872933],"domain_scores_gemma":[0.99973935,0.00006260994,0.00004434598,0.00003100585,0.00006993175,0.000052724066],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00017779955,0.00013656844,0.00017653294,0.0004517669,0.00030718406,0.0008954816,0.000216175,0.00031902318,0.0008817968],"category_scores_gemma":[0.00034319595,0.0003234735,0.00020902794,0.00037489692,0.00029382826,0.0008024953,0.00041329602,0.00065775926,0.00044923043],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.000103399405,0.000005798657,0.0032930113,0.000021915022,0.000005589996,0.000042213072,0.00012269853,0.00019392271,0.99148023,0.0010271203,0.00012694242,0.0035771455],"study_design_scores_gemma":[0.000026813243,0.000107486136,0.76060146,0.000028889826,0.000042686297,0.00042679848,0.00050157716,0.005113795,0.21861385,0.002327309,0.012171907,0.00003744637],"about_ca_topic_score_codex":0.002833179,"about_ca_topic_score_gemma":0.0040718373,"teacher_disagreement_score":0.002833179,"about_ca_system_score_codex":0.00076260447,"about_ca_system_score_gemma":0.0003102657,"threshold_uncertainty_score":0.005633414},"labels":[],"label_agreement":null},{"id":"W2078462908","doi":"10.1038/ng.478","title":"Genetic variants in TPMT and COMT are associated with hearing loss in children receiving cisplatin chemotherapy","year":2009,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Cancer therapeutics and mechanisms","field":"Biochemistry, Genetics and Molecular Biology","cited_by":328,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"BC Children's Hospital; Children's & Women's Health Centre of British Columbia; Montreal Heart Institute; Université de Montréal; Child and Family Research Institute; University of British Columbia","funders":"Canadian Institutes of Health Research","keywords":"Ototoxicity; Thiopurine methyltransferase; Cisplatin; Hearing loss; Biology; Oncology; Cohort; Single-nucleotide polymorphism; Candidate gene; Pharmacogenetics; Genetics; Genetic predisposition; Bioinformatics; Pharmacology; Internal medicine; Chemotherapy; Gene; Genotype; Medicine; Audiology; Disease","score_opus":0.005476407377881841,"score_gpt":0.23682257147785105,"score_spread":0.2313461640999692,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2078462908","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.998845,0.0002065165,0.00015653772,0.0001461982,0.000014729224,0.0000075276735,0.00013658307,0.000013495391,0.0004733072],"genre_scores_gemma":[0.9994537,0.00013419036,0.00013300926,0.000034243232,0.00002059892,0.0000050263707,0.00006862772,0.0000081956,0.00014240309],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9991345,0.0001246846,0.00012230843,0.00018011984,0.0002766357,0.00016171989],"domain_scores_gemma":[0.9968285,0.0011946361,0.0012928033,0.00008035186,0.00019302101,0.00041075645],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00033307105,0.0011154036,0.000647889,0.0022111845,0.000734617,0.0007237059,0.0008937079,0.0010979736,0.002982853],"category_scores_gemma":[0.0043753516,0.00056168507,0.0007720852,0.0021786285,0.0010827946,0.00051131635,0.0006349776,0.0011904157,0.00032265944],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0012687359,0.00020595962,0.9409991,0.00007184952,0.00019491964,0.038721807,0.0005441305,0.000285579,0.01271688,0.00015511061,0.00040601057,0.00443],"study_design_scores_gemma":[0.00006106721,0.0004954153,0.9140841,0.000042875192,0.0003252118,0.08026971,0.00057747395,0.0006750099,0.002801682,0.00014887277,0.0004897438,0.000028840437],"about_ca_topic_score_codex":0.00651706,"about_ca_topic_score_gemma":0.0030525983,"teacher_disagreement_score":0.00651706,"about_ca_system_score_codex":0.0004699834,"about_ca_system_score_gemma":0.00061089505,"threshold_uncertainty_score":0.012958229},"labels":[],"label_agreement":null},{"id":"W2078540517","doi":"10.1038/ng.3279","title":"COPA mutations impair ER-Golgi transport and cause hereditary autoimmune-mediated lung disease and arthritis","year":2015,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Cell Adhesion Molecules Research","field":"Medicine","cited_by":399,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Hospital for Sick Children","funders":"National Institute of Allergy and Infectious Diseases; National Institute of Arthritis and Musculoskeletal and Skin Diseases; National Institute of Neurological Disorders and Stroke; National Human Genome Research Institute; National Heart, Lung, and Blood Institute","keywords":"Biology; Autoimmunity; Exome sequencing; Immunology; Autoantibody; Phenotype; Immune dysregulation; Autoimmune disease; Genetics; Cell biology; Gene; Immune system; Antibody","score_opus":0.013544529010278021,"score_gpt":0.2954112506079901,"score_spread":0.2818667215977121,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2078540517","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9928167,0.0013586307,0.003007119,0.00024022782,0.00010187194,0.000028425306,0.0006943672,0.0001926974,0.0015598572],"genre_scores_gemma":[0.99686724,0.00032842555,0.0015739452,0.000070858,0.000023159897,0.000013917577,0.00024279437,0.00008860672,0.0007910177],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.999258,0.00018181955,0.00015643226,0.00013981316,0.00017369275,0.00009024305],"domain_scores_gemma":[0.99881905,0.00030254567,0.00047926663,0.0000930382,0.0000637667,0.00024231346],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00031040833,0.0019857765,0.00051448314,0.0014526455,0.00057725125,0.0007021905,0.0008933809,0.0016215652,0.0043606674],"category_scores_gemma":[0.000849705,0.0006046431,0.00086997356,0.00076970144,0.0012498992,0.00050236256,0.0010644312,0.0009924453,0.0009179225],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00062149734,0.00012651017,0.004051377,0.0000946849,0.00022294465,0.005594612,0.00010235662,0.00045522733,0.9843327,0.0008164182,0.00044484297,0.0031368283],"study_design_scores_gemma":[0.0004323347,0.0005959159,0.10355111,0.00008959273,0.0007533489,0.06055696,0.00042011397,0.010016018,0.8139018,0.0016331966,0.007949742,0.000099818266],"about_ca_topic_score_codex":0.0024391878,"about_ca_topic_score_gemma":0.0029018747,"teacher_disagreement_score":0.0043606674,"about_ca_system_score_codex":0.0006478133,"about_ca_system_score_gemma":0.0004242961,"threshold_uncertainty_score":0.014587939},"labels":[],"label_agreement":null},{"id":"W2078675213","doi":"10.1038/ng.3052","title":"Genome-wide association study identifies multiple susceptibility loci for pancreatic cancer","year":2014,"lang":"en","type":"review","venue":"Nature Genetics","topic":"Pancreatic and Hepatic Oncology Research","field":"Medicine","cited_by":345,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Public Health Ontario; University of Toronto; Lunenfeld-Tanenbaum Research Institute; Cancer Care Ontario; Mount Sinai Hospital","funders":"National Institute of General Medical Sciences; National Institute of Environmental Health Sciences; National Institute for Health and Care Research; National Cancer Institute; National Institutes of Health; U.S. Department of Health and Human Services; Cancer Research UK; Conquer Cancer Foundation; World Health Organization; Howard Hughes Medical Institute","keywords":"Pancreatic cancer; Biology; Locus (genetics); Odds ratio; Genome-wide association study; Genetics; Allele; PDX1; Genome; Confidence interval; Genetic association; Oncology; Cancer; Internal medicine; Genotype; Single-nucleotide polymorphism; Gene; Medicine","score_opus":0.051161927191049276,"score_gpt":0.4176669783244997,"score_spread":0.36650505113345044,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2078675213","genre_codex":"review","genre_gemma":"review","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"review","genre_consensus":"review","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.00012297531,0.99837327,0.00013966752,0.00069291505,0.00020959982,0.0000023792666,0.000031768846,0.000007412337,0.00042006784],"genre_scores_gemma":[0.00085128745,0.9977449,0.00020311563,0.0004898055,0.0003766392,0.000003592684,0.000053765805,0.0000012668017,0.0002756128],"study_design_codex":"design_other","study_design_gemma":"observational","domain_scores_codex":[0.9997137,0.00005234656,0.00004828797,0.00006632337,0.00009496861,0.000024303234],"domain_scores_gemma":[0.99904555,0.00055444724,0.000121139776,0.0000275257,0.00017323965,0.00007805261],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0011195436,0.0009704355,0.0016863357,0.0018577707,0.00020662925,0.0007956063,0.0010585407,0.0013614246,0.0022917935],"category_scores_gemma":[0.0014033233,0.0003082252,0.00070476456,0.0023432537,0.0005454663,0.000831529,0.00081053836,0.0018908764,0.0009727468],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00017309956,0.000050058574,0.0015571191,0.009736511,0.00040492034,0.00032710086,0.000026938367,0.00023331287,0.0010898534,0.0016618603,0.04053033,0.9442088],"study_design_scores_gemma":[0.0001307005,0.0001386387,0.009914822,0.0070526907,0.0013990694,0.0024492573,0.00011965454,0.00018131698,0.0006823073,0.0051925406,0.9726697,0.00006916665],"about_ca_topic_score_codex":0.0013527406,"about_ca_topic_score_gemma":0.0031210347,"teacher_disagreement_score":0.0022917935,"about_ca_system_score_codex":0.0005545576,"about_ca_system_score_gemma":0.0012593894,"threshold_uncertainty_score":0.0076668262},"labels":[],"label_agreement":null},{"id":"W2079362912","doi":"10.1038/ng.787","title":"Genome-wide association study identifies susceptibility loci for IgA nephropathy","year":2011,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Renal Diseases and Glomerulopathies","field":"Medicine","cited_by":624,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Calgary","funders":"National Center for Research Resources; National Institute of Diabetes and Digestive and Kidney Diseases; Howard Hughes Medical Institute","keywords":"Biology; Genome-wide association study; Nephropathy; Genetics; Allele; Locus (genetics); Odds ratio; Genetic association; Minor allele frequency; Genetic variation; Allele frequency; Immunology; Single-nucleotide polymorphism; Genotype; Gene; Internal medicine; Diabetes mellitus; Endocrinology; Medicine","score_opus":0.017456780160502523,"score_gpt":0.2806427841152856,"score_spread":0.2631860039547831,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2079362912","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9980161,0.0005155697,0.00045100643,0.00021021556,0.000027438999,0.000005397425,0.00019257673,0.000022533843,0.00055914896],"genre_scores_gemma":[0.9990515,0.0001448611,0.00034745006,0.000046285822,0.000029329256,0.000003526699,0.00013035243,0.0000095764735,0.00023714494],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99899775,0.00043011506,0.00009187201,0.00025586606,0.00011934118,0.000105190345],"domain_scores_gemma":[0.9981463,0.0007707123,0.0004199139,0.0001963103,0.0001186366,0.00034816502],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0013527155,0.000647162,0.00050155685,0.0017368632,0.0009060122,0.0007840654,0.00069474295,0.0010491782,0.0023014238],"category_scores_gemma":[0.00201556,0.00044361834,0.0010511441,0.0016319893,0.00062726095,0.00031594376,0.0006815893,0.001113454,0.00019141908],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0034600934,0.00039411016,0.9526291,0.00006205747,0.0023525357,0.0016485503,0.00028170602,0.000225275,0.031443086,0.00034801033,0.0006311712,0.006524261],"study_design_scores_gemma":[0.000119945915,0.00022947171,0.99522924,0.000008978048,0.0008233438,0.0011787569,0.00014322036,0.0005287971,0.0010072904,0.0002954523,0.00042258468,0.000012928488],"about_ca_topic_score_codex":0.0027733133,"about_ca_topic_score_gemma":0.0035706144,"teacher_disagreement_score":0.0027733133,"about_ca_system_score_codex":0.00025107377,"about_ca_system_score_gemma":0.00035068791,"threshold_uncertainty_score":0.0076990128},"labels":[],"label_agreement":null},{"id":"W2080077971","doi":"10.1038/ng.981","title":"Genome-wide association study identifies FCGR2A as a susceptibility locus for Kawasaki disease","year":2011,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Kawasaki Disease and Coronary Complications","field":"Medicine","cited_by":356,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Université de Montréal; SickKids Foundation; Hospital for Sick Children; University of Toronto","funders":"National Heart, Lung, and Blood Institute","keywords":"Kawasaki disease; Locus (genetics); Biology; Genome-wide association study; Genetics; Allele; Disease; Single-nucleotide polymorphism; Genetic association; SNP; Immunology; Gene; Genotype; Medicine; Internal medicine","score_opus":0.022876529096638124,"score_gpt":0.3034502387384264,"score_spread":0.2805737096417883,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2080077971","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99796426,0.00051728194,0.00046933666,0.000254189,0.000034809902,0.000006735759,0.00014766179,0.000018158302,0.00058756565],"genre_scores_gemma":[0.99903667,0.00013053622,0.0003297564,0.000055059863,0.000055923087,0.000004976272,0.00011696238,0.000007156626,0.00026295413],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9993292,0.00026679644,0.00006385028,0.0001536537,0.00010963796,0.000076860524],"domain_scores_gemma":[0.99878067,0.0005393968,0.0002534702,0.00011328399,0.00009954085,0.00021367079],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00084231846,0.000787233,0.00055306137,0.0015995267,0.0008072351,0.00070668844,0.00072138984,0.0010690152,0.0021142],"category_scores_gemma":[0.001981749,0.000366603,0.001041766,0.00163228,0.00050474884,0.00025016698,0.00046554088,0.0010152541,0.00019639301],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0057642027,0.00033232296,0.9167074,0.000084314386,0.0021022246,0.0067973277,0.0005116304,0.00031103488,0.058745097,0.00044120755,0.0011301098,0.0070731766],"study_design_scores_gemma":[0.00018582461,0.00021334806,0.9915242,0.000015653397,0.0010707382,0.0032232373,0.0002037442,0.0009160566,0.0017085425,0.000263464,0.00065844174,0.000016679744],"about_ca_topic_score_codex":0.005501515,"about_ca_topic_score_gemma":0.0038768104,"teacher_disagreement_score":0.005501515,"about_ca_system_score_codex":0.00025165087,"about_ca_system_score_gemma":0.000309515,"threshold_uncertainty_score":0.010939002},"labels":[],"label_agreement":null},{"id":"W2080235308","doi":"10.1038/ng.823","title":"Genome partitioning of genetic variation for complex traits using common SNPs","year":2011,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Genetic Associations and Epidemiology","field":"Biochemistry, Genetics and Molecular Biology","cited_by":956,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Université de Montréal; Montreal Heart Institute","funders":"National Human Genome Research Institute; Canadian Institutes of Health Research","keywords":"Biology; Single-nucleotide polymorphism; Genetics; Genetic variation; Variation (astronomy); Genome-wide association study; Evolutionary biology; Computational biology; Genome; Genotype; Gene","score_opus":0.04457439900603231,"score_gpt":0.29793962466608975,"score_spread":0.2533652256600574,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2080235308","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9616069,0.00043714067,0.036301434,0.00017042797,0.000021705684,0.000032434535,0.00039183183,0.000098145865,0.00093997543],"genre_scores_gemma":[0.9909089,0.00009044898,0.0084147155,0.000055123764,0.000012156247,0.000020941108,0.00023461373,0.000035884706,0.0002272647],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99595886,0.0020551858,0.00012228462,0.0013243026,0.00028727096,0.00025206877],"domain_scores_gemma":[0.9952814,0.003325333,0.00046843084,0.00058049726,0.00012076612,0.00022360068],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0024138556,0.0007975191,0.00091644254,0.0034642697,0.00065680215,0.0011481948,0.0009496676,0.0007946914,0.0035292762],"category_scores_gemma":[0.0050746053,0.00051713415,0.0018458798,0.002339882,0.0010701199,0.0006332953,0.0013780259,0.0010180004,0.00021261105],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0030999195,0.00027623257,0.6458622,0.00035570964,0.009265202,0.001359418,0.0018854609,0.018666562,0.21984959,0.017057067,0.0009979482,0.08132464],"study_design_scores_gemma":[0.00021463899,0.00028696845,0.9251957,0.000052311298,0.0014419355,0.0009662933,0.0005373095,0.042030036,0.0057946476,0.022082195,0.0012898558,0.00010802982],"about_ca_topic_score_codex":0.0053246133,"about_ca_topic_score_gemma":0.005969803,"teacher_disagreement_score":0.0053246133,"about_ca_system_score_codex":0.0005090289,"about_ca_system_score_gemma":0.00030727693,"threshold_uncertainty_score":0.012765825},"labels":[],"label_agreement":null},{"id":"W2080775789","doi":"10.1038/ng.749","title":"Genetic deficiency of tartrate-resistant acid phosphatase associated with skeletal dysplasia, cerebral calcifications and autoimmunity","year":2011,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Bone and Dental Protein Studies","field":"Medicine","cited_by":186,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Toronto; Mount Sinai Hospital","funders":"","keywords":"Biology; Osteopontin; Pathogenesis; Autoimmunity; Immunology; Dysplasia; Immune system; Endocrinology; Genetics; Cancer research","score_opus":0.017574295054701306,"score_gpt":0.24764964227757363,"score_spread":0.23007534722287232,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2080775789","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99293596,0.0015167928,0.00131491,0.00052283565,0.00006799979,0.000022736016,0.00025709934,0.00006166283,0.0033000675],"genre_scores_gemma":[0.9978677,0.00055785844,0.0007253769,0.0000723879,0.0000844964,0.000008450997,0.000102519494,0.00001665347,0.000564571],"study_design_codex":"case_report","study_design_gemma":"observational","domain_scores_codex":[0.9993647,0.00011433004,0.00013088429,0.00012592375,0.0001677814,0.00009644445],"domain_scores_gemma":[0.998212,0.0007093759,0.0005214154,0.000104355604,0.00014854374,0.0003043612],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00047098417,0.0019292185,0.00065968285,0.0031840722,0.0007690005,0.0005652692,0.0008389702,0.0017829684,0.002400141],"category_scores_gemma":[0.002577739,0.0006612946,0.0005186798,0.0016268371,0.0019340042,0.00048479292,0.0006789665,0.00092054514,0.00028342227],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0039000374,0.00043751052,0.13727792,0.00035995123,0.00066177134,0.5961143,0.0008328153,0.0006947826,0.24450926,0.003100109,0.0011931178,0.010918413],"study_design_scores_gemma":[0.0003537015,0.0007873934,0.25723043,0.00008220351,0.0010978461,0.6708834,0.0006427254,0.0017447384,0.060583804,0.0024554755,0.004039546,0.00009878486],"about_ca_topic_score_codex":0.003349941,"about_ca_topic_score_gemma":0.0023106951,"teacher_disagreement_score":0.003349941,"about_ca_system_score_codex":0.00048234023,"about_ca_system_score_gemma":0.0006265503,"threshold_uncertainty_score":0.0080292225},"labels":[],"label_agreement":null},{"id":"W2080815080","doi":"10.1038/ng.743","title":"Drosophila Piwi functions in Hsp90-mediated suppression of phenotypic variation","year":2010,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Heat shock proteins research","field":"Biochemistry, Genetics and Molecular Biology","cited_by":164,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Stem Cell Network","funders":"Eunice Kennedy Shriver National Institute of Child Health and Human Development; National Institute of General Medical Sciences; National Institutes of Health","keywords":"Piwi-interacting RNA; Biology; Transposable element; Genetics; RasiRNA; Gene silencing; Epigenetics; Phenotype; RNA interference; RNA; Small RNA; Drosophila melanogaster; Gene; Genome","score_opus":0.007051126832052051,"score_gpt":0.2763088386804476,"score_spread":0.26925771184839553,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2080815080","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9826031,0.0008454353,0.010231943,0.00020107937,0.00005176274,0.000030555664,0.0009300574,0.000571127,0.004534962],"genre_scores_gemma":[0.99407876,0.0002656246,0.0015523911,0.00008107972,0.0000071730337,0.00002135175,0.00045485614,0.00015283038,0.0033858982],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99976426,0.000036996033,0.000023494185,0.00006952924,0.00006676691,0.000039007315],"domain_scores_gemma":[0.9997632,0.000034351586,0.00008076393,0.000038809238,0.000017236529,0.00006558701],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00016228981,0.0008825836,0.00029515685,0.000609501,0.00027864688,0.00049758214,0.00069877954,0.00040832252,0.0025197398],"category_scores_gemma":[0.00025973807,0.00036786406,0.000306803,0.00037683218,0.000360065,0.00030679628,0.00090385875,0.0010129272,0.0007908865],"study_design_candidate":"bench_or_experimental","study_design_consensus":"bench_or_experimental","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.000051411906,0.000007527078,0.0001856559,0.000014657591,0.000006290237,0.00006643963,0.000008298632,0.000079423015,0.99796236,0.00027888332,0.000041185733,0.0012978201],"study_design_scores_gemma":[0.00003533392,0.00005889748,0.02004509,0.000008989263,0.000028029965,0.00059479807,0.000039331924,0.004202503,0.97197366,0.00022674185,0.00276899,0.000017666009],"about_ca_topic_score_codex":0.0010407879,"about_ca_topic_score_gemma":0.0023508887,"teacher_disagreement_score":0.0025197398,"about_ca_system_score_codex":0.000698072,"about_ca_system_score_gemma":0.00022545911,"threshold_uncertainty_score":0.0084293485},"labels":[],"label_agreement":null},{"id":"W2080964315","doi":"10.1038/72842","title":"Fus deficiency in mice results in defective B-lymphocyte development and activation, high levels of chromosomal instability and perinatal death","year":2000,"lang":"en","type":"article","venue":"Nature Genetics","topic":"RNA Research and Splicing","field":"Biochemistry, Genetics and Molecular Biology","cited_by":289,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Manitoba","funders":"National Center for Research Resources; National Cancer Institute; National Human Genome Research Institute","keywords":"Biology; Transcription factor; Transcription (linguistics); Gene; Genome instability; Cell biology; Molecular biology; Chromosome instability; Genetics; DNA; DNA damage; Chromosome","score_opus":0.009743243139620026,"score_gpt":0.26031279455266826,"score_spread":0.2505695514130482,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2080964315","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9689764,0.004447836,0.010896145,0.0006185848,0.00013335691,0.000089664034,0.0075198417,0.0017563815,0.005561784],"genre_scores_gemma":[0.975695,0.0023826594,0.0053051757,0.00023503607,0.00006669358,0.0001063546,0.002465292,0.00060083845,0.013143002],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99932206,0.00009819634,0.00010127837,0.00015503977,0.0001915514,0.0001318901],"domain_scores_gemma":[0.998541,0.0002687271,0.0006338458,0.00011829411,0.00005324342,0.00038494333],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00036894047,0.0018714623,0.0008417239,0.0034262158,0.0006729461,0.00097647216,0.00094160077,0.0015957594,0.0059131566],"category_scores_gemma":[0.00036463127,0.0009302336,0.00064143905,0.0010068993,0.0014669298,0.0006635335,0.0008733085,0.0016702231,0.0013801234],"study_design_candidate":"bench_or_experimental","study_design_consensus":"bench_or_experimental","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0007219705,0.00004059508,0.00035536973,0.0000672588,0.000039605075,0.00086089165,0.000035226756,0.00020600612,0.9950271,0.00056821835,0.00016349072,0.0019142223],"study_design_scores_gemma":[0.00011572465,0.00028880374,0.0065803556,0.000040735835,0.000112113914,0.004192623,0.00012068248,0.0010038883,0.98349977,0.0006318692,0.0033782453,0.0000351394],"about_ca_topic_score_codex":0.0013679634,"about_ca_topic_score_gemma":0.0022820549,"teacher_disagreement_score":0.0059131566,"about_ca_system_score_codex":0.0007278579,"about_ca_system_score_gemma":0.000457061,"threshold_uncertainty_score":0.01978153},"labels":[],"label_agreement":null},{"id":"W2081501101","doi":"10.1038/ng.734","title":"Common variants in P2RY11 are associated with narcolepsy","year":2010,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Sleep and Wakefulness Research","field":"Neuroscience","cited_by":236,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Centre Hospitalier de l’Université de Montréal; Université de Montréal","funders":"National Institute of Allergy and Infectious Diseases; National Institute of Neurological Disorders and Stroke; National Institute of Mental Health; National Institutes of Health","keywords":"Biology; Narcolepsy; Genetics; Computational biology; Neuroscience; Neurology","score_opus":0.02177321217129219,"score_gpt":0.3002951239935511,"score_spread":0.27852191182225894,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2081501101","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.98979807,0.0015266394,0.0022789245,0.0010608186,0.0003503681,0.000086158325,0.0018188951,0.00011681815,0.0029634456],"genre_scores_gemma":[0.99511117,0.00041536454,0.0011876908,0.00029716516,0.00030998752,0.000045800844,0.0008874865,0.000074636635,0.0016707588],"study_design_codex":"case_report","study_design_gemma":"observational","domain_scores_codex":[0.9986387,0.0003020068,0.00024193907,0.00041179074,0.00025286342,0.00015273697],"domain_scores_gemma":[0.9966023,0.0013740844,0.0013222622,0.00018047924,0.000142296,0.00037855672],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0006321757,0.0035350919,0.0011749436,0.0025270346,0.001263359,0.001109965,0.0017440727,0.0042818603,0.010585341],"category_scores_gemma":[0.0030602042,0.00066075433,0.0020479106,0.0027644995,0.001385662,0.0006774647,0.0010876004,0.001827334,0.0012549823],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.013695065,0.000753249,0.25745386,0.00090303074,0.00524271,0.35099146,0.0029566728,0.0027269388,0.32687324,0.0036826862,0.007726526,0.026994584],"study_design_scores_gemma":[0.0013345251,0.0015186825,0.6976869,0.00043395592,0.003456789,0.25751498,0.0012887275,0.0030304645,0.01853696,0.003306595,0.011550542,0.00034097114],"about_ca_topic_score_codex":0.0033018652,"about_ca_topic_score_gemma":0.003880073,"teacher_disagreement_score":0.010585341,"about_ca_system_score_codex":0.00040193,"about_ca_system_score_gemma":0.00039716423,"threshold_uncertainty_score":0.035411477},"labels":[],"label_agreement":null},{"id":"W2082947145","doi":"10.1038/ng.714","title":"Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies","year":2010,"lang":"en","type":"review","venue":"Nature Genetics","topic":"Hypothalamic control of reproductive hormones","field":"Medicine","cited_by":511,"is_retracted":false,"has_abstract":false,"route_ca_aff":false,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"","funders":"National Center for Advancing Translational Sciences; National Center for Research Resources; National Institute of Dental and Craniofacial Research; National Institute of Arthritis and Musculoskeletal and Skin Diseases; National Institute of Diabetes and Digestive and Kidney Diseases; National Human Genome Research Institute; Danmarks Grundforskningsfond; National Institute of Mental Health; National Heart, Lung, and Blood Institute; National Institute on Aging; National Institute on Alcohol Abuse and Alcoholism; March of Dimes Foundation; Helmholtz Zentrum München; National Health and Medical Research Council; Medical Research Council; National Institutes of Health; U.S. Public Health Service; Centre for Medical Systems Biology; Hjartavernd; University of Bristol; Egmont Fonden; Amgen; Chinese Society of Clinical Oncology; Fondation Leenaards; Compagnia di San Paolo; Augustinus Fonden; National Institute on Drug Abuse; Hjärt-Lungfonden; Fondazione Cariplo; Vetenskapsrådet; Scottish Government; Ministère de l'Education Nationale, de l'Enseignement Superieur et de la Recherche; Ministero della Salute; European Regional Development Fund; Bundesministerium für Bildung und Forschung; Cancer Research UK; Wellcome Trust; Münchner Zentrum für Gesundheitswissenschaften; Erasmus Medisch Centrum; Stiftelsen för Strategisk Forskning; Schweizerischer Nationalfonds zur Förderung der Wissenschaftlichen Forschung; National Research Foundation; Svenska Läkaresällskapet; Nederlandse Organisatie voor Wetenschappelijk Onderzoek; National Institute on Minority Health and Health Disparities; European Commission; National Cancer Institute; Eunice Kennedy Shriver National Institute of Child Health and Human Development; GlaxoSmithKline; National Science Foundation; American Heart Association; Canadian Institutes of Health Research; Juvenile Diabetes Research Foundation International","keywords":"Biology; Menarche; Genome-wide association study; Genetics; Gene; Genetic association; Body mass index; Genome; Genotype; Single-nucleotide polymorphism; Endocrinology","score_opus":0.11429585545812496,"score_gpt":0.39290886542611714,"score_spread":0.2786130099679922,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2082947145","genre_codex":"review","genre_gemma":"review","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"review","genre_consensus":"review","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.00514318,0.9933762,0.00062573666,0.00030712973,0.000079933816,0.0000061215264,0.00021870274,0.000017609671,0.00022535866],"genre_scores_gemma":[0.039990246,0.95622486,0.0020934055,0.00036524562,0.00021675095,0.000020115214,0.0007667027,0.000009767985,0.00031289237],"study_design_codex":"design_other","study_design_gemma":"meta_analysis","domain_scores_codex":[0.9993104,0.00014412246,0.00011615728,0.0002304672,0.00015296336,0.000045951896],"domain_scores_gemma":[0.9981342,0.0013245776,0.0002633221,0.000062530286,0.000148984,0.000066461274],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0017771348,0.0014349567,0.003395444,0.0024390297,0.0002281764,0.0011492097,0.0013628535,0.0010634211,0.0016040121],"category_scores_gemma":[0.0024692805,0.00044765175,0.002355233,0.0040394836,0.00037476167,0.00067633996,0.00073093374,0.00074367307,0.0003550632],"study_design_candidate":"meta_analysis","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0018905099,0.00010617382,0.0816295,0.03435365,0.030393112,0.0037309444,0.00024474104,0.0012906402,0.00916235,0.0010272649,0.011019903,0.82515126],"study_design_scores_gemma":[0.0011006662,0.00088163844,0.5703524,0.013695898,0.1465125,0.02217228,0.00080460217,0.0014096181,0.004992164,0.008829266,0.22883298,0.0004160446],"about_ca_topic_score_codex":0.0026332967,"about_ca_topic_score_gemma":0.0058618276,"teacher_disagreement_score":0.003395444,"about_ca_system_score_codex":0.00048542413,"about_ca_system_score_gemma":0.0013984038,"threshold_uncertainty_score":0.00939846},"labels":[],"label_agreement":null},{"id":"W2084090304","doi":"10.1038/ng1707","title":"Cooperative and antagonistic interactions between Sall4 and Tbx5 pattern the mouse limb and heart","year":2005,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Congenital heart defects research","field":"Biochemistry, Genetics and Molecular Biology","cited_by":171,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Toronto; Heart and Stroke Foundation; Hospital for Sick Children","funders":"","keywords":"Forelimb; Biology; GATA4; Zinc finger transcription factor; Transcription factor; Limb development; Zinc finger; Heart development; Heart disease; Gene; Embryonic stem cell; Embryonic heart; Morphogenesis; Genetics; Anatomy; Cell biology; Internal medicine; Medicine","score_opus":0.011539056281024671,"score_gpt":0.31370226400372886,"score_spread":0.30216320772270416,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2084090304","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.98165554,0.0027852054,0.009441172,0.0003846128,0.000081390936,0.000017568751,0.00019363676,0.00016898676,0.00527189],"genre_scores_gemma":[0.9911157,0.00032787933,0.0029858493,0.00022086417,0.00002038014,0.000029699853,0.0002875205,0.00007910593,0.0049331705],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99914527,0.00017435955,0.000059507624,0.00015738618,0.00024887334,0.00021459542],"domain_scores_gemma":[0.9993333,0.00013835348,0.00018429325,0.000096341224,0.000069584756,0.00017810588],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00059634127,0.0004685862,0.00042618025,0.0007664995,0.0004338039,0.0010781438,0.0010314555,0.00064970134,0.0032840944],"category_scores_gemma":[0.00057486177,0.00073417043,0.0005774692,0.00024148387,0.0008388626,0.00067314244,0.0017553052,0.0013249429,0.0016997455],"study_design_candidate":"bench_or_experimental","study_design_consensus":"bench_or_experimental","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00009574343,0.000008264804,0.00074348174,0.000025630789,0.000010642279,0.00006408281,0.000017434279,0.00011003735,0.9969169,0.00054836954,0.00007831607,0.0013809807],"study_design_scores_gemma":[0.000105969935,0.00021100642,0.0388297,0.000027052773,0.0000797135,0.00102559,0.00033218725,0.005403738,0.9468841,0.00086205266,0.0062125176,0.00002638691],"about_ca_topic_score_codex":0.000478344,"about_ca_topic_score_gemma":0.0016142635,"teacher_disagreement_score":0.0032840944,"about_ca_system_score_codex":0.0006894335,"about_ca_system_score_gemma":0.00029192228,"threshold_uncertainty_score":0.010986388},"labels":[],"label_agreement":null},{"id":"W2084224210","doi":"10.1038/ng.884","title":"Mutations in NBEAL2, encoding a BEACH protein, cause gray platelet syndrome","year":2011,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Platelet Disorders and Treatments","field":"Medicine","cited_by":275,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Hospital for Sick Children; SickKids Foundation; University of Toronto","funders":"National Center for Research Resources; National Institute of Diabetes and Digestive and Kidney Diseases; National Heart, Lung, and Blood Institute; Canadian Institutes of Health Research","keywords":"Biology; Gene; Intron; Genetics; RNA; Platelet; genomic DNA; Platelet activation; Messenger RNA; Computational biology; Immunology","score_opus":0.021835352789604127,"score_gpt":0.27507738260883957,"score_spread":0.25324202981923544,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2084224210","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.987171,0.00144946,0.0037132974,0.001164423,0.00011457455,0.000028976056,0.00040385587,0.00017096307,0.005783416],"genre_scores_gemma":[0.9971944,0.0002587625,0.0012042909,0.0001564065,0.000031957523,0.000008253666,0.00017017935,0.000028648014,0.0009471108],"study_design_codex":"case_report","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99988544,0.000013084233,0.000010228625,0.000031975018,0.000037110847,0.000022204704],"domain_scores_gemma":[0.9997814,0.00007773127,0.000050158083,0.000011957778,0.0000112035705,0.00006757011],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00008310205,0.0008199637,0.0003623727,0.00058178604,0.00036678914,0.0003175206,0.0003015208,0.0009969501,0.0026677689],"category_scores_gemma":[0.0005219822,0.00016302403,0.00026571093,0.00041405988,0.0007363756,0.00023062785,0.00048363328,0.0006803838,0.000419873],"study_design_candidate":"bench_or_experimental","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0014135323,0.000118443924,0.03217906,0.00017887435,0.00022553484,0.48062557,0.0004623424,0.0008367011,0.44695956,0.0031724554,0.004253548,0.029574424],"study_design_scores_gemma":[0.00048229462,0.00039730177,0.085707776,0.000081147125,0.00039972994,0.7431086,0.00056480843,0.0055299704,0.14521651,0.004417724,0.01402207,0.00007211554],"about_ca_topic_score_codex":0.0012660741,"about_ca_topic_score_gemma":0.0011927749,"teacher_disagreement_score":0.0026677689,"about_ca_system_score_codex":0.0004021075,"about_ca_system_score_gemma":0.00020616813,"threshold_uncertainty_score":0.008924544},"labels":[],"label_agreement":null},{"id":"W2084708009","doi":"10.1038/ng.215","title":"Deletion polymorphism upstream of IRGM associated with altered IRGM expression and Crohn's disease","year":2008,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Mycobacterium research and diagnosis","field":"Medicine","cited_by":661,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Toronto; Mount Sinai Hospital; Montreal Heart Institute; Université de Montréal","funders":"National Institute of Allergy and Infectious Diseases; National Institute of Diabetes and Digestive and Kidney Diseases; National Heart, Lung, and Blood Institute","keywords":"Biology; Genetics; Linkage disequilibrium; Single-nucleotide polymorphism; ATG16L1; Genome-wide association study; Autophagy; Disease; Genetic association; Population; Haplotype; Allele; Genotype; Gene","score_opus":0.013717557041833198,"score_gpt":0.264120258224963,"score_spread":0.2504027011831298,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2084708009","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99659365,0.00025737743,0.0012785437,0.00019697261,0.00007399424,0.000030694853,0.00048332236,0.000052661777,0.0010327322],"genre_scores_gemma":[0.99780566,0.000053862896,0.0010041416,0.00010980415,0.00006310611,0.000014683647,0.00039854992,0.00004128382,0.00050890946],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9993218,0.00016375804,0.000103920436,0.0001852856,0.00010194164,0.0001232632],"domain_scores_gemma":[0.9981275,0.00079718203,0.0005788241,0.00011940985,0.000092817856,0.00028417737],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00027721148,0.0010622082,0.00074900914,0.0013020737,0.00064820366,0.0005035959,0.0006719496,0.0017113888,0.004978704],"category_scores_gemma":[0.0012139393,0.00035768686,0.00084923394,0.00091150665,0.0009093752,0.00022559975,0.00045290476,0.0013332912,0.0011427363],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.005392337,0.0005486353,0.029875718,0.00018172013,0.00023449038,0.031389177,0.0005281231,0.00048296925,0.9239823,0.00081229245,0.0005310149,0.006041168],"study_design_scores_gemma":[0.0011615871,0.0028415455,0.59660244,0.00032647722,0.0012924549,0.13232142,0.0008932378,0.004657013,0.24836442,0.0013281767,0.010001552,0.00020973542],"about_ca_topic_score_codex":0.0010011218,"about_ca_topic_score_gemma":0.0007597263,"teacher_disagreement_score":0.004978704,"about_ca_system_score_codex":0.00029761324,"about_ca_system_score_gemma":0.00025995038,"threshold_uncertainty_score":0.016655445},"labels":[],"label_agreement":null},{"id":"W2084730888","doi":"10.1038/ng792","title":"Independent genome-wide scans identify a chromosome 18 quantitative-trait locus influencing dyslexia","year":2001,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Reading and Literacy Development","field":"Psychology","cited_by":270,"is_retracted":false,"has_abstract":false,"route_ca_aff":false,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"","funders":"National Institute of Mental Health; National Institutes of Health; National Institute of Child Health and Human Development; Natural Sciences and Engineering Research Council of Canada; Wellcome Trust","keywords":"Dyslexia; Biology; Quantitative trait locus; Genetic linkage; Genetics; Locus (genetics); Trait; Genome Scan; Linkage (software); Developmental psychology; Psychology; Allele; Reading (process); Gene; Microsatellite; Linguistics","score_opus":0.023471144588854045,"score_gpt":0.34011018964823675,"score_spread":0.31663904505938273,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2084730888","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9948926,0.00040363293,0.0015926447,0.0002575438,0.000033174227,0.00003860607,0.001723351,0.00006514641,0.0009932779],"genre_scores_gemma":[0.99613994,0.00021931644,0.0014940778,0.00019358392,0.000024769195,0.000038006878,0.0010553531,0.000027802978,0.0008070814],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99941516,0.000083003884,0.00004251169,0.000250837,0.000099403485,0.000109155255],"domain_scores_gemma":[0.9982784,0.0008223043,0.00040794956,0.00009336513,0.00012760333,0.00027040535],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0006143581,0.0008877732,0.00057561207,0.0022224719,0.0005549632,0.00065123785,0.00067374605,0.00096770166,0.004269011],"category_scores_gemma":[0.001991681,0.0002790071,0.00077224156,0.0012517071,0.0006715235,0.00019754728,0.0007034715,0.00079602073,0.0003118273],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0073396196,0.0003688186,0.614062,0.000219427,0.0019862126,0.006174258,0.001399371,0.0005078893,0.33384937,0.00071388914,0.0014961147,0.03188298],"study_design_scores_gemma":[0.00027779862,0.000272892,0.9886513,0.00002267202,0.00053865614,0.0022172786,0.00021716818,0.00042243776,0.0059838817,0.0003003055,0.0010763105,0.000019357945],"about_ca_topic_score_codex":0.0056317816,"about_ca_topic_score_gemma":0.00837024,"teacher_disagreement_score":0.0056317816,"about_ca_system_score_codex":0.00034906153,"about_ca_system_score_gemma":0.00035526959,"threshold_uncertainty_score":0.014281213},"labels":[],"label_agreement":null},{"id":"W2085543266","doi":"10.1038/79918","title":"Genome rearrangement by replication-directed translocation","year":2000,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Genomics and Phylogenetic Studies","field":"Biochemistry, Genetics and Molecular Biology","cited_by":196,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Toronto","funders":"","keywords":"Biology; Genome; Genetics; Gene; Bacterial genome size; Origin of replication; Genome evolution; Operon; Gene rearrangement; Haemophilus influenzae; Escherichia coli; Bacteria","score_opus":0.005537381470466901,"score_gpt":0.23432204035143708,"score_spread":0.2287846588809702,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2085543266","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.92152053,0.003375491,0.058504388,0.0012861904,0.00044592953,0.00020639492,0.0003421719,0.0010244838,0.013294436],"genre_scores_gemma":[0.98041177,0.0008776439,0.011857529,0.00018059702,0.000037339636,0.00007790014,0.00041287814,0.00011762359,0.0060268575],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9995715,0.00009052051,0.000019718573,0.00015204825,0.000055072793,0.00011118137],"domain_scores_gemma":[0.99960023,0.00014085452,0.000075386364,0.00010679614,0.000023827415,0.000052818887],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0004262853,0.00046497656,0.0004881439,0.00048040345,0.0005190401,0.00074961997,0.0005376455,0.0010953799,0.0033294712],"category_scores_gemma":[0.00083959836,0.00044289598,0.0006309839,0.00037452794,0.00075598067,0.0009799444,0.0009950711,0.0015840221,0.00181752],"study_design_candidate":"bench_or_experimental","study_design_consensus":"bench_or_experimental","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0002596317,0.000033832544,0.00034916945,0.00008111464,0.000013063601,0.0003513331,0.00006693372,0.0006313435,0.9867648,0.004993193,0.000336325,0.0061193756],"study_design_scores_gemma":[0.0002082661,0.00051353034,0.003585683,0.000019377974,0.000042333057,0.0024934902,0.00017772977,0.0061119683,0.96795684,0.0053954907,0.013432137,0.00006310296],"about_ca_topic_score_codex":0.00054946664,"about_ca_topic_score_gemma":0.00064323883,"teacher_disagreement_score":0.0033294712,"about_ca_system_score_codex":0.00059130637,"about_ca_system_score_gemma":0.00036502237,"threshold_uncertainty_score":0.01113826},"labels":[{"model":"gemma","categories":[],"domain":null,"study_design":"bench_or_experimental","genre":"empirical","about_ca_system":false,"about_ca_topic":false,"confidence":"low"},{"model":"gpt","categories":[],"domain":null,"study_design":"bench_or_experimental","genre":"empirical","about_ca_system":false,"about_ca_topic":false,"confidence":"high"}],"label_agreement":"agree"},{"id":"W2086281676","doi":"10.1038/ng718","title":"The UDP-N-acetylglucosamine 2-epimerase/N-acetylmannosamine kinase gene is mutated in recessive hereditary inclusion body myopathy","year":2001,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Inflammatory Myopathies and Dermatomyositis","field":"Medicine","cited_by":528,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Montreal Neurological Institute and Hospital","funders":"","keywords":"Missense mutation; Genetics; Biology; Myopathy; Haplotype; Compound heterozygosity; Mutation; Founder effect; Gene; Allele","score_opus":0.005628173590749505,"score_gpt":0.259824250176465,"score_spread":0.25419607658571547,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2086281676","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9916148,0.0012870975,0.0018998743,0.00041735618,0.00015294435,0.00003190163,0.00033043328,0.0001347602,0.0041308235],"genre_scores_gemma":[0.9968305,0.00032867727,0.00091490085,0.00007855889,0.00007389553,0.000009692919,0.00013169786,0.000034002693,0.0015979955],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9996176,0.00008072206,0.000062149156,0.000071240356,0.00009881807,0.00006940523],"domain_scores_gemma":[0.99943787,0.00021919658,0.000132161,0.000021004786,0.00005466427,0.00013506293],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00027165454,0.0014205127,0.0006608366,0.0015169659,0.00063739135,0.00042872617,0.00060266105,0.0015241599,0.0027060425],"category_scores_gemma":[0.001157671,0.0003725038,0.0005069572,0.00053811766,0.0008996692,0.0003611281,0.00059890136,0.0007119984,0.0006609462],"study_design_candidate":"bench_or_experimental","study_design_consensus":"bench_or_experimental","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0036957648,0.00022445411,0.020743532,0.00038166097,0.0002817462,0.35617566,0.0007818488,0.00136766,0.59631497,0.0028588127,0.0020661834,0.01510778],"study_design_scores_gemma":[0.00084465626,0.001486031,0.21053779,0.00021126197,0.0010297889,0.46225458,0.0007697133,0.008793708,0.30034804,0.002059886,0.0115417335,0.00012274129],"about_ca_topic_score_codex":0.0022703002,"about_ca_topic_score_gemma":0.0014035151,"teacher_disagreement_score":0.0027060425,"about_ca_system_score_codex":0.0005545872,"about_ca_system_score_gemma":0.0002767879,"threshold_uncertainty_score":0.009052634},"labels":[],"label_agreement":null},{"id":"W2087236782","doi":"10.1038/ng.627","title":"Genome-wide meta-analyses identify three loci associated with primary biliary cirrhosis","year":2010,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Liver Diseases and Immunity","field":"Medicine","cited_by":396,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Mount Sinai Hospital; London Health Sciences Centre; University of Toronto; University Health Network; Dalhousie University; University of Calgary; University of Alberta","funders":"National Institute of Diabetes and Digestive and Kidney Diseases; Canadian Institutes of Health Research; National Institutes of Health; American Gastroenterological Association","keywords":"Biology; Genome-wide association study; Primary biliary cirrhosis; Odds ratio; Cohort; Genetics; Allele; Meta-analysis; Internal medicine; Single-nucleotide polymorphism; Genotype; Gene; Medicine; Immunology","score_opus":0.04377607920382486,"score_gpt":0.31872057845053475,"score_spread":0.2749444992467099,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2087236782","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9709684,0.019759983,0.0048160753,0.0012490584,0.00023059778,0.000027491802,0.00133637,0.00019088425,0.001421054],"genre_scores_gemma":[0.99771833,0.0010660082,0.0005869353,0.00010856507,0.00006223028,0.000007736294,0.00024564785,0.000022902434,0.0001816783],"study_design_codex":"observational","study_design_gemma":"meta_analysis","domain_scores_codex":[0.9968617,0.0012272515,0.0002407187,0.001037503,0.0003039744,0.0003288139],"domain_scores_gemma":[0.99495465,0.003068451,0.00067278306,0.0006789709,0.00022086769,0.0004042826],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0031630865,0.0020801993,0.0025465835,0.0022762388,0.0008973069,0.0019514061,0.0013599149,0.0019494903,0.0025515726],"category_scores_gemma":[0.006212413,0.001019972,0.0073019927,0.0034618753,0.000765753,0.0007024599,0.0013779452,0.0016524997,0.00021716932],"study_design_candidate":"meta_analysis","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0064541693,0.00010090931,0.8606557,0.00055345154,0.108115844,0.0013951366,0.00023431305,0.0018497457,0.009960517,0.00043657786,0.0009421031,0.009301571],"study_design_scores_gemma":[0.00051732647,0.0004465634,0.9042971,0.00009507421,0.08539703,0.0012839108,0.00030043788,0.0036144615,0.0016570622,0.0013609956,0.00096415565,0.00006590165],"about_ca_topic_score_codex":0.0054726475,"about_ca_topic_score_gemma":0.0081132315,"teacher_disagreement_score":0.0054726475,"about_ca_system_score_codex":0.0004174355,"about_ca_system_score_gemma":0.0006781834,"threshold_uncertainty_score":0.016728163},"labels":[],"label_agreement":null},{"id":"W2087387372","doi":"10.1038/ng.640","title":"Genome-wide association study identifies variants in the CFH region associated with host susceptibility to meningococcal disease","year":2010,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Bacterial Infections and Vaccines","field":"Immunology and Microbiology","cited_by":289,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Institute of Infection and Immunity","funders":"Wellcome Trust","keywords":"Biology; Genetics; Genome-wide association study; Meningococcal disease; Host (biology); Genome; Genetic association; Disease; Neisseria meningitidis; Gene; Genotype; Single-nucleotide polymorphism; Bacteria","score_opus":0.008879665677184354,"score_gpt":0.25181871563967795,"score_spread":0.2429390499624936,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2087387372","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9980861,0.00055152137,0.00038290292,0.00015602798,0.000026624497,0.0000061573523,0.00029893543,0.000012623132,0.0004790298],"genre_scores_gemma":[0.9994192,0.000085452964,0.00018444414,0.000043600216,0.000018378403,0.0000028093223,0.00008877876,0.0000048548236,0.0001525517],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9992587,0.00025807702,0.00006661755,0.00022161062,0.00009760204,0.0000974377],"domain_scores_gemma":[0.9985091,0.0007622463,0.0003416889,0.00010282066,0.000082388186,0.00020172761],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00082303194,0.00062031444,0.00047402031,0.0013758878,0.00077019265,0.00053926755,0.000503078,0.0012184109,0.0020490063],"category_scores_gemma":[0.0016991203,0.00027998985,0.0007215119,0.0015350751,0.0006397738,0.00023468654,0.00041772312,0.0010201421,0.00012951012],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0069490466,0.00030635757,0.91080374,0.000096891956,0.0025812315,0.0033330396,0.0004646332,0.0005814554,0.065001845,0.0005262067,0.0010008807,0.008354705],"study_design_scores_gemma":[0.00013511936,0.00020410238,0.99465513,0.000016524515,0.0006341911,0.0014268939,0.00014723842,0.0008341776,0.0012574078,0.00023046542,0.0004399743,0.000018649007],"about_ca_topic_score_codex":0.0072688796,"about_ca_topic_score_gemma":0.007641259,"teacher_disagreement_score":0.0072688796,"about_ca_system_score_codex":0.00024483362,"about_ca_system_score_gemma":0.00027932116,"threshold_uncertainty_score":0.014453113},"labels":[],"label_agreement":null},{"id":"W2088442470","doi":"10.1038/ng1010-813","title":"Public data archives for genomic structural variation","year":2010,"lang":"en","type":"letter","venue":"Nature Genetics","topic":"Genomic variations and chromosomal abnormalities","field":"Biochemistry, Genetics and Molecular Biology","cited_by":76,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"SickKids Foundation; Hospital for Sick Children; University of Toronto","funders":"National Institutes of Health","keywords":"Biology; Variation (astronomy); Genetics; Structural variation; Computational biology; Evolutionary biology; Genome; Gene","score_opus":0.02247251874293043,"score_gpt":0.252540339681519,"score_spread":0.23006782093858857,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2088442470","genre_codex":"dataset","genre_gemma":"commentary","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"commentary","genre_consensus":null,"domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.0020785592,0.003043486,0.0061266525,0.24137735,0.02673484,0.0003851091,0.60621923,0.009037576,0.104997285],"genre_scores_gemma":[0.019673435,0.006778123,0.016896185,0.105256796,0.028058445,0.0016999338,0.63780457,0.0039902143,0.17984231],"study_design_codex":"not_applicable","study_design_gemma":"not_applicable","domain_scores_codex":[0.9984805,0.00026641658,0.00025010703,0.00015946329,0.00065343356,0.00019006211],"domain_scores_gemma":[0.9831702,0.007117671,0.0010654596,0.00339618,0.0035893018,0.001661096],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0034524684,0.00090378604,0.0015923164,0.003837892,0.0012702668,0.0024642914,0.003189642,0.0073622875,0.20471816],"category_scores_gemma":[0.021894967,0.0007074202,0.00062970817,0.004364771,0.00076626136,0.002324206,0.0022024456,0.006447513,0.1385802],"study_design_candidate":"not_applicable","study_design_consensus":"not_applicable","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00007165002,0.000013565862,0.000127203,0.000049953993,0.000003957379,0.000107966494,0.000007950401,0.000049132417,0.00015968274,0.0010327671,0.9922184,0.0061579566],"study_design_scores_gemma":[0.0001516426,0.000013162811,0.0012132328,0.00012575366,0.000009108809,0.00027522715,0.000023752922,0.00037722735,0.00049204595,0.0051457584,0.99215204,0.000021022099],"about_ca_topic_score_codex":0.0057621803,"about_ca_topic_score_gemma":0.0081518525,"teacher_disagreement_score":0.20471816,"about_ca_system_score_codex":0.0018979333,"about_ca_system_score_gemma":0.0024688519,"threshold_uncertainty_score":0.68485045},"labels":[],"label_agreement":null},{"id":"W2090803844","doi":"10.1038/ng1819","title":"A genetic signature of interspecies variations in gene expression","year":2006,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Fungal and yeast genetics research","field":"Biochemistry, Genetics and Molecular Biology","cited_by":289,"is_retracted":false,"has_abstract":false,"route_ca_aff":false,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"","funders":"Weizmann Institute of Science; University Health Network; Harvard University","keywords":"Biology; Gene; Genetics; Gene expression; Promoter; TATA box; Regulation of gene expression; Phenotype; Functional divergence; Evolutionary biology; Computational biology; Gene family","score_opus":0.005589514399701219,"score_gpt":0.2570306892984499,"score_spread":0.2514411748987487,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2090803844","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99376655,0.00029738777,0.0026994145,0.000060850118,0.00002791256,0.000015015422,0.00077648147,0.00017383869,0.0021825018],"genre_scores_gemma":[0.99652004,0.00013281922,0.0009465543,0.000107594635,0.000020091406,0.000027313601,0.0007281294,0.00011770002,0.0013998549],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9994912,0.000040674673,0.000047543803,0.00020874255,0.00013422444,0.00007749505],"domain_scores_gemma":[0.99826103,0.00067830476,0.00034793717,0.00032804493,0.000117344665,0.00026736074],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00027852683,0.000313418,0.0004957788,0.0011903516,0.00027472223,0.0005744896,0.00043014318,0.00047023123,0.0028165102],"category_scores_gemma":[0.0008424826,0.00032642737,0.00042884346,0.00073296594,0.0005012899,0.0004146326,0.0010078729,0.0012861136,0.00052978314],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00007392758,0.000021450089,0.0010646669,0.0000120964605,0.000015862239,0.00004665383,0.000020046722,0.00003990312,0.9974759,0.00013859387,0.00002349975,0.0010674031],"study_design_scores_gemma":[0.00004029797,0.000431262,0.45363247,0.000016293843,0.00010942899,0.003536156,0.0001909352,0.001943182,0.5372533,0.0011502964,0.0016283777,0.000067978086],"about_ca_topic_score_codex":0.00041785714,"about_ca_topic_score_gemma":0.00070029526,"teacher_disagreement_score":0.0028165102,"about_ca_system_score_codex":0.0003223111,"about_ca_system_score_gemma":0.00020489824,"threshold_uncertainty_score":0.009422123},"labels":[],"label_agreement":null},{"id":"W2090830396","doi":"10.1038/ng.464","title":"Mutations in FAM134B, encoding a newly identified Golgi protein, cause severe sensory and autonomic neuropathy","year":2009,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Cellular transport and secretion","field":"Biochemistry, Genetics and Molecular Biology","cited_by":256,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Credit Valley Hospital","funders":"","keywords":"Biology; Dorsal root ganglion; Neuroscience; Sensory system; Golgi apparatus; Gene knockdown; Cell biology; Genetics; Apoptosis; Endoplasmic reticulum","score_opus":0.008315726229226907,"score_gpt":0.2343153630369029,"score_spread":0.22599963680767599,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2090830396","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9913556,0.0014824857,0.0035202303,0.0006237687,0.00025222296,0.000044199456,0.00091676647,0.00024611462,0.0015586648],"genre_scores_gemma":[0.99573284,0.00033190867,0.002394934,0.00012314187,0.000050734972,0.000017926766,0.0004865067,0.000060420854,0.00080153474],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99980646,0.000026524738,0.000020828442,0.00004448502,0.00006871122,0.00003286225],"domain_scores_gemma":[0.9994771,0.00010576533,0.00017423525,0.000014103953,0.00003407041,0.00019474175],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00018137624,0.002029704,0.00067404815,0.0008733269,0.00054459256,0.0003438911,0.00048552867,0.0019963782,0.0016077177],"category_scores_gemma":[0.0008926607,0.00034877096,0.00044598064,0.00048548056,0.00094889157,0.00026368393,0.00059603475,0.0006749623,0.00062816526],"study_design_candidate":"bench_or_experimental","study_design_consensus":"bench_or_experimental","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.001057255,0.00013700123,0.012269392,0.00022215833,0.00018290653,0.09278994,0.00021679566,0.0007352429,0.88033044,0.00069664035,0.0020710444,0.009291138],"study_design_scores_gemma":[0.0009907562,0.0017790762,0.29225066,0.00035647332,0.00072234287,0.48893493,0.0007276071,0.0109394295,0.17996582,0.003135244,0.019805072,0.00039255052],"about_ca_topic_score_codex":0.0025161074,"about_ca_topic_score_gemma":0.0025178636,"teacher_disagreement_score":0.0025161074,"about_ca_system_score_codex":0.00042613453,"about_ca_system_score_gemma":0.00028238707,"threshold_uncertainty_score":0.0053783655},"labels":[],"label_agreement":null},{"id":"W2091765691","doi":"10.1038/ng1630","title":"Genome-wide analysis of mouse transcripts using exon microarrays and factor graphs","year":2005,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Gene expression and cancer classification","field":"Biochemistry, Genetics and Molecular Biology","cited_by":47,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Hospital for Sick Children; Lunenfeld-Tanenbaum Research Institute; Mount Sinai Hospital; Canada Research Chairs; University of New Brunswick; University of Toronto","funders":"","keywords":"Biology; Exon; Genetics; Gene; Polyadenylation; DNA microarray; Genome; Exon trapping; Microarray; Complementary DNA; Microarray analysis techniques; Computational biology; Alternative splicing; RNA; Gene expression","score_opus":0.013681376392036485,"score_gpt":0.26483593195669114,"score_spread":0.25115455556465466,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2091765691","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9493071,0.0012592055,0.036170583,0.00012176585,0.000017012102,0.000026372036,0.010764461,0.00059432996,0.0017392596],"genre_scores_gemma":[0.9274464,0.0011697696,0.045396876,0.0001460821,0.000023794359,0.00010840866,0.022869473,0.00020483763,0.0026344752],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99972004,0.00003369503,0.000011964708,0.00011769292,0.00007014674,0.00004648056],"domain_scores_gemma":[0.99964786,0.00017003978,0.00008301435,0.00003225079,0.000040885043,0.00002594693],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00038898466,0.00027959346,0.00030962864,0.0011402793,0.00031186864,0.00036680492,0.00022402577,0.00023169105,0.001305345],"category_scores_gemma":[0.00038663336,0.0001998116,0.0004873168,0.001439801,0.00022725886,0.00017918799,0.00021684715,0.00038054024,0.00027872156],"study_design_candidate":"bench_or_experimental","study_design_consensus":"bench_or_experimental","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.000420543,0.000030095249,0.013427416,0.00011781465,0.00013223726,0.00008008007,0.00007106477,0.002297491,0.96442133,0.0011863663,0.00054410606,0.017271483],"study_design_scores_gemma":[0.00008936157,0.00042606864,0.47488335,0.000036621597,0.00048476446,0.0007278041,0.00019489478,0.029184459,0.47052285,0.005115699,0.01827017,0.0000638879],"about_ca_topic_score_codex":0.001959981,"about_ca_topic_score_gemma":0.007114877,"teacher_disagreement_score":0.001959981,"about_ca_system_score_codex":0.00028387227,"about_ca_system_score_gemma":0.00021872035,"threshold_uncertainty_score":0.004366815},"labels":[],"label_agreement":null},{"id":"W2092433469","doi":"10.1038/ng1260","title":"Pyruvate kinase deficiency in mice protects against malaria","year":2003,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Hemoglobinopathies and Related Disorders","field":"Medicine","cited_by":133,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Biotechnology Research Institute; Montreal General Hospital; McGill University","funders":"","keywords":"Biology; Plasmodium chabaudi; Malaria; Pyruvate kinase deficiency; Congenic; Genetics; Allele; Locus (genetics); Immunology; Virology; Gene; Plasmodium falciparum; Pyruvate kinase; Parasitemia","score_opus":0.006005622309565329,"score_gpt":0.2370458488773977,"score_spread":0.23104022656783238,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2092433469","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9812744,0.0028608884,0.0057003745,0.0019594012,0.00036995803,0.00012326168,0.0029936666,0.0012925272,0.0034254915],"genre_scores_gemma":[0.9841388,0.0019776982,0.0030246363,0.00042654225,0.00011064123,0.00013893569,0.0010793675,0.00036518593,0.008738276],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9995413,0.00009032306,0.000042737265,0.00012755072,0.00007205771,0.00012605895],"domain_scores_gemma":[0.99903715,0.00009531622,0.00037083484,0.00011628199,0.000042493422,0.0003379286],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00038819987,0.0014296616,0.0008509191,0.0017102682,0.00048288683,0.00090520066,0.00091879396,0.0014550615,0.0046852725],"category_scores_gemma":[0.00037875955,0.00082625175,0.00052875647,0.0005469663,0.0011823047,0.0007033726,0.00052052,0.0029310584,0.0009494826],"study_design_candidate":"bench_or_experimental","study_design_consensus":"bench_or_experimental","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0023874603,0.00022577432,0.0003097353,0.00008451041,0.000055523265,0.00022611239,0.000046636553,0.00020284209,0.99276465,0.0009783262,0.0004708068,0.0022477382],"study_design_scores_gemma":[0.0012363329,0.0018082018,0.0058058794,0.000073603616,0.00031191614,0.0014253126,0.000190427,0.002387357,0.9765414,0.0014478734,0.008712898,0.00005886498],"about_ca_topic_score_codex":0.0010636376,"about_ca_topic_score_gemma":0.0012877445,"teacher_disagreement_score":0.0046852725,"about_ca_system_score_codex":0.0006672118,"about_ca_system_score_gemma":0.00053449086,"threshold_uncertainty_score":0.015673816},"labels":[],"label_agreement":null},{"id":"W2092645079","doi":"10.1038/ng.2007.57","title":"Genome-wide analysis of transcript isoform variation in humans","year":2008,"lang":"en","type":"article","venue":"Nature Genetics","topic":"RNA Research and Splicing","field":"Biochemistry, Genetics and Molecular Biology","cited_by":309,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Centre Hospitalier Universitaire Sainte-Justine; Ontario Institute for Cancer Research; McGill University and Génome Québec Innovation Centre; McGill University","funders":"Canadian Institutes of Health Research; Genome Canada","keywords":"Biology; International HapMap Project; Genetics; Alternative splicing; Polyadenylation; Exon; Gene isoform; Gene; Untranslated region; Single-nucleotide polymorphism; Genetic variation; Intron; Human genome; Genome; Gene expression; Genotype; RNA","score_opus":0.00981776769859182,"score_gpt":0.26297208478840634,"score_spread":0.2531543170898145,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2092645079","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.997863,0.00042583194,0.00055871165,0.00003101115,0.0000042754727,0.0000025649058,0.00079702784,0.000015270547,0.00030243714],"genre_scores_gemma":[0.99759656,0.00019849661,0.0007544949,0.000055490927,0.000011069899,0.0000051855573,0.00094923837,0.000024320321,0.00040515166],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.99978775,0.000040939773,0.000012880196,0.00010919897,0.000034140467,0.000015222152],"domain_scores_gemma":[0.99976367,0.00011302645,0.0000544405,0.000027287086,0.000018466799,0.00002307025],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0003198305,0.00016425639,0.00028918375,0.0006339916,0.00021765167,0.0003066217,0.0001564547,0.00029301617,0.0011420198],"category_scores_gemma":[0.00041690722,0.0001614879,0.00024493027,0.00059008837,0.00019781379,0.00007513937,0.00017288794,0.00024757255,0.00018072008],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0028193558,0.000057824287,0.34312835,0.00013311014,0.0011662423,0.0016219389,0.00047715145,0.0013624122,0.615533,0.0005467181,0.000865381,0.032288454],"study_design_scores_gemma":[0.000032622374,0.0000804995,0.985058,0.000006830024,0.00017208539,0.0016506229,0.000054239263,0.00068923755,0.010365244,0.00023673233,0.0016455761,0.000008426734],"about_ca_topic_score_codex":0.0009051157,"about_ca_topic_score_gemma":0.0018016608,"teacher_disagreement_score":0.0011420198,"about_ca_system_score_codex":0.000094313466,"about_ca_system_score_gemma":0.000060297654,"threshold_uncertainty_score":0.003820479},"labels":[],"label_agreement":null},{"id":"W2093148342","doi":"10.1038/ng2072","title":"Loss of GLIS2 causes nephronophthisis in humans and mice by increased apoptosis and fibrosis","year":2007,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Genetic and Kidney Cyst Diseases","field":"Biochemistry, Genetics and Molecular Biology","cited_by":239,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Manitoba","funders":"National Institute of Diabetes and Digestive and Kidney Diseases","keywords":"Nephronophthisis; Positional cloning; Biology; Cancer research; Phenotype; Fibrosis; Gene; Mutant; Mutation; Kidney; Genetics; Pathology; Medicine","score_opus":0.0034184725894792376,"score_gpt":0.2356430107420702,"score_spread":0.23222453815259095,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2093148342","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99206626,0.00079149974,0.0038225714,0.00043693246,0.000064145635,0.000030724626,0.0011462985,0.0003638072,0.0012778508],"genre_scores_gemma":[0.9945351,0.00045097576,0.001986844,0.00013064627,0.000023634802,0.00004132362,0.0004721248,0.00009878857,0.0022605155],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99967885,0.00005401571,0.00003559124,0.00009045584,0.00009407309,0.000047003025],"domain_scores_gemma":[0.99969745,0.000044127453,0.0001227289,0.00002966343,0.000013725972,0.00009229354],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00025409437,0.00097225106,0.00050684897,0.0013162306,0.0003062063,0.0004017703,0.0003681103,0.0008269764,0.003151523],"category_scores_gemma":[0.00027605655,0.00054150115,0.00053913705,0.0003983883,0.0012087034,0.00024654646,0.00059614837,0.0011125231,0.00041006596],"study_design_candidate":"bench_or_experimental","study_design_consensus":"bench_or_experimental","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0011375705,0.00005140218,0.002024501,0.00006519961,0.00009868921,0.0024869654,0.00006612582,0.000344541,0.9894868,0.0005841196,0.00046564767,0.0031884853],"study_design_scores_gemma":[0.0006936035,0.00092876214,0.07776374,0.000047779788,0.00045533763,0.038266648,0.000333064,0.0049646604,0.8660117,0.0017156915,0.008745339,0.00007365307],"about_ca_topic_score_codex":0.00138934,"about_ca_topic_score_gemma":0.0019331798,"teacher_disagreement_score":0.003151523,"about_ca_system_score_codex":0.0003228459,"about_ca_system_score_gemma":0.00037836583,"threshold_uncertainty_score":0.010542929},"labels":[],"label_agreement":null},{"id":"W2093176323","doi":"10.1038/ng.2669","title":"The Capsella rubella genome and the genomic consequences of rapid mating system evolution","year":2013,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Plant and animal studies","field":"Agricultural and Biological Sciences","cited_by":471,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"McGill University; University of Toronto","funders":"FP7 Food, Agriculture and Fisheries, Biotechnology; Uppsala Multidisciplinary Center for Advanced Computational Science; Alfred P. Sloan Foundation; Natural Sciences and Engineering Research Council of Canada; Grantová Agentura České Republiky; Genome Canada; European Regional Development Fund; Max-Planck-Gesellschaft; Office of Science; Agence Nationale de la Recherche; Vetenskapsrådet; National Science Foundation","keywords":"Biology; Selfing; Outcrossing; Genetics; Genome; Mating system; Evolutionary biology; Gene; Mating; Botany; Population","score_opus":0.012502339968861848,"score_gpt":0.1792234002613331,"score_spread":0.16672106029247125,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2093176323","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9930929,0.0032074412,0.0018156554,0.00028192325,0.000024387942,0.000005522722,0.00040607905,0.00010568855,0.0010604218],"genre_scores_gemma":[0.9954348,0.0012222438,0.0015223019,0.00015748087,0.000028771692,0.00000571087,0.00095464714,0.000028418028,0.000645642],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9998987,0.000012713422,0.000004867187,0.00003291829,0.000031265605,0.000019583233],"domain_scores_gemma":[0.9996276,0.000090502625,0.00011101194,0.00004758981,0.00005951092,0.00006381297],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0002340588,0.00022874516,0.00014991072,0.00051778945,0.00026162525,0.00033717213,0.00033459297,0.00032195638,0.00050479814],"category_scores_gemma":[0.0005060886,0.00013727385,0.00018140183,0.00037071618,0.00020795844,0.00024663814,0.00029755846,0.00046354134,0.0001584885],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0002550736,0.000021759826,0.019253964,0.00009141366,0.000038162376,0.00045634463,0.00018404935,0.00050457305,0.9602939,0.00046391244,0.00022417727,0.0182128],"study_design_scores_gemma":[0.000030416786,0.00023827769,0.8639614,0.000032618165,0.00008889448,0.002219833,0.00031778205,0.0017669499,0.11694817,0.0016847239,0.012664401,0.000046600457],"about_ca_topic_score_codex":0.002048817,"about_ca_topic_score_gemma":0.0025914095,"teacher_disagreement_score":0.002048817,"about_ca_system_score_codex":0.00029033297,"about_ca_system_score_gemma":0.0001558875,"threshold_uncertainty_score":0.004073739},"labels":[],"label_agreement":null},{"id":"W2093297340","doi":"10.1038/ng.3202","title":"Combined hereditary and somatic mutations of replication error repair genes result in rapid onset of ultra-hypermutated cancers","year":2015,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Genetic factors in colorectal cancer","field":"Medicine","cited_by":381,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Ontario Institute for Cancer Research; University of Toronto; SickKids Foundation; Mount Sinai Hospital; Hospital for Sick Children","funders":"Canadian Institutes of Health Research; Cancer Research UK; Wellcome Trust","keywords":"Biology; Somatic cell; Genetics; Gene; Replication (statistics); Mutation; Virology","score_opus":0.026373173759289957,"score_gpt":0.3107184453822134,"score_spread":0.28434527162292345,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2093297340","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9939241,0.0013474562,0.0021509961,0.00005796976,0.000028888335,0.000014545208,0.0005737162,0.00020994946,0.0016924179],"genre_scores_gemma":[0.9972398,0.00040791903,0.0009672213,0.00002289551,0.000015417536,0.000006098088,0.00026817477,0.00004571717,0.0010266013],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9997342,0.00004102282,0.000029289182,0.00007014567,0.00007752218,0.000047786038],"domain_scores_gemma":[0.9994591,0.00011383035,0.00020309453,0.000061590086,0.000036616624,0.00012580359],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0001752237,0.0003188119,0.00032512075,0.0014366515,0.00017445981,0.0002985576,0.00024717255,0.00034588197,0.0032955802],"category_scores_gemma":[0.000567157,0.0003446458,0.00032529596,0.00060438324,0.0002137634,0.00025883428,0.00054049405,0.000420081,0.00052077085],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0018686447,0.000121738674,0.055185474,0.00009170258,0.00013925153,0.009676334,0.00006859383,0.00020220288,0.91702867,0.00070670026,0.00051164377,0.014399028],"study_design_scores_gemma":[0.00008083408,0.00078364444,0.5650706,0.000019383959,0.0002766812,0.10315991,0.00016595965,0.0012493742,0.32200712,0.00039736604,0.006748371,0.000040716066],"about_ca_topic_score_codex":0.00039674895,"about_ca_topic_score_gemma":0.0005227012,"teacher_disagreement_score":0.0032955802,"about_ca_system_score_codex":0.00017820281,"about_ca_system_score_gemma":0.00014400657,"threshold_uncertainty_score":0.011024773},"labels":[{"model":"gemma","categories":[],"domain":null,"study_design":"observational","genre":"empirical","about_ca_system":false,"about_ca_topic":false,"confidence":"low"},{"model":"gpt","categories":[],"domain":null,"study_design":"bench_or_experimental","genre":"empirical","about_ca_system":false,"about_ca_topic":false,"confidence":"high"}],"label_agreement":"split"},{"id":"W2093362931","doi":"10.1038/ng.2274","title":"A genome-wide approach accounting for body mass index identifies genetic variants influencing fasting glycemic traits and insulin resistance","year":2012,"lang":"en","type":"review","venue":"Nature Genetics","topic":"Pancreatic function and diabetes","field":"Medicine","cited_by":888,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Université Laval; Ontario Institute for Cancer Research; Lunenfeld-Tanenbaum Research Institute; Université de Sherbrooke","funders":"National Center for Advancing Translational Sciences; National Institute of Diabetes and Digestive and Kidney Diseases; National Heart, Lung, and Blood Institute; National Center for Research Resources; National Institute of Mental Health; Medical Research Council; Novo Nordisk Fonden; British Heart Foundation; Wellcome Trust","keywords":"Biology; Insulin resistance; Body mass index; Glycemic; Genetics; Glycemic index; Genome-wide association study; Resistance (ecology); Genome; Obesity; Insulin; Internal medicine; Bioinformatics; Endocrinology; Genotype; Gene; Single-nucleotide polymorphism; Medicine","score_opus":0.02485499532984866,"score_gpt":0.28330900433040956,"score_spread":0.2584540090005609,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2093362931","genre_codex":"review","genre_gemma":"review","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"review","genre_consensus":"review","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.0010859341,0.9961021,0.0012551056,0.0006230023,0.0002649721,0.0000073784477,0.00009215485,0.000022016908,0.00054731395],"genre_scores_gemma":[0.005349059,0.990339,0.002301962,0.00084115635,0.0003697137,0.000014310298,0.00021242001,0.000006810657,0.0005655395],"study_design_codex":"design_other","study_design_gemma":"observational","domain_scores_codex":[0.99973744,0.000053994358,0.000028759692,0.000090758134,0.000069248184,0.000019803643],"domain_scores_gemma":[0.99940455,0.00038358406,0.00007498582,0.000023386632,0.00008160511,0.000031877786],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0011110906,0.0015589686,0.0024962574,0.0013435647,0.00016096781,0.00085413357,0.0011990115,0.0011379139,0.0016286246],"category_scores_gemma":[0.0009771573,0.00029598418,0.0011589812,0.0016764787,0.00039981923,0.00058805675,0.00051900675,0.0014219169,0.00061621756],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00030375973,0.00006827984,0.0031844296,0.005338638,0.0015540895,0.00054607185,0.000027962058,0.00041708173,0.0038720279,0.001328778,0.009083114,0.97427577],"study_design_scores_gemma":[0.00054106605,0.0007202346,0.07587117,0.010222545,0.012242849,0.010240553,0.00031325253,0.0015603217,0.006817084,0.017984044,0.8631692,0.00031774555],"about_ca_topic_score_codex":0.0014256096,"about_ca_topic_score_gemma":0.0029112939,"teacher_disagreement_score":0.0024962574,"about_ca_system_score_codex":0.00037427718,"about_ca_system_score_gemma":0.0007383948,"threshold_uncertainty_score":0.0058760643},"labels":[],"label_agreement":null},{"id":"W2094074562","doi":"10.1038/ng.683","title":"Mutations in WDR62, encoding a centrosome-associated protein, cause microcephaly with simplified gyri and abnormal cortical architecture","year":2010,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Microtubule and mitosis dynamics","field":"Biochemistry, Genetics and Molecular Biology","cited_by":286,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Health Sciences Centre; Alberta Children's Hospital; University of Alberta Hospital; University of Calgary","funders":"Fogarty International Center; Eunice Kennedy Shriver National Institute of Child Health and Human Development; Howard Hughes Medical Institute; U.S. Public Health Service; National Center for Research Resources; National Institute of Neurological Disorders and Stroke; National Human Genome Research Institute","keywords":"Microcephaly; Biology; Gene; Genetics; Locus (genetics); Phenotype; Cerebral cortex; Cell biology; Neuroscience","score_opus":0.003636538149422772,"score_gpt":0.22861317711521498,"score_spread":0.2249766389657922,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2094074562","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9944174,0.0004932603,0.0021690282,0.00026991082,0.00006703175,0.00005628046,0.000520642,0.00022542497,0.0017811458],"genre_scores_gemma":[0.99604803,0.00033105825,0.0018857842,0.000060046143,0.000035871093,0.000024687675,0.00027052284,0.0000408654,0.0013031942],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99980694,0.00002594965,0.000024822873,0.000037315396,0.000083031904,0.00002193406],"domain_scores_gemma":[0.99947387,0.00016369816,0.00021024072,0.000027656566,0.000023148466,0.000101368736],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.000121988676,0.0015801009,0.0004163119,0.0012136162,0.00049223535,0.00028752655,0.00032907585,0.0007745598,0.0010752702],"category_scores_gemma":[0.00069817447,0.00029718142,0.00032022104,0.00062454614,0.0010797061,0.00020730078,0.0005469535,0.00056044094,0.00034684714],"study_design_candidate":"bench_or_experimental","study_design_consensus":"bench_or_experimental","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0015970919,0.0002789893,0.017432176,0.0003126553,0.00041051855,0.20243876,0.00079157675,0.002704715,0.7437024,0.0025366885,0.0030068185,0.024787582],"study_design_scores_gemma":[0.0008427687,0.0012511966,0.28860816,0.00013237513,0.00076752936,0.33985344,0.0008235496,0.012782328,0.33835837,0.0039719664,0.01236608,0.00024228111],"about_ca_topic_score_codex":0.0025670426,"about_ca_topic_score_gemma":0.0046504373,"teacher_disagreement_score":0.0025670426,"about_ca_system_score_codex":0.00049358077,"about_ca_system_score_gemma":0.00030465744,"threshold_uncertainty_score":0.0051042438},"labels":[],"label_agreement":null},{"id":"W2095167019","doi":"10.1038/87218","title":"A detailed transcript map of the human chromosome 12p12.3 tumor suppressor locus: the usefulness of an integrative approach","year":2001,"lang":"en","type":"article","venue":"Nature Genetics","topic":"RNA modifications and cancer","field":"Biochemistry, Genetics and Molecular Biology","cited_by":0,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Centre Hospitalier Universitaire Sainte-Justine","funders":"","keywords":"Locus (genetics); Biology; Suppressor; Genetics; Chromosome; Gene; Gene mapping; Computational biology","score_opus":0.013184354371981021,"score_gpt":0.25643460821587194,"score_spread":0.24325025384389093,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2095167019","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.72864854,0.008526919,0.23235674,0.0013878179,0.00029153956,0.0004406125,0.013521958,0.0025246604,0.012301151],"genre_scores_gemma":[0.792776,0.009467351,0.14190885,0.00037165708,0.00019809863,0.00035840628,0.039634522,0.00062234025,0.014662768],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9999305,0.00000527941,0.0000040813125,0.000024467123,0.000021184085,0.000014486976],"domain_scores_gemma":[0.9999287,0.000018518083,0.000010295009,0.000010492417,0.00001354325,0.000018393068],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00010875029,0.0004840389,0.0004314974,0.0006251563,0.00041011212,0.00039936134,0.00031541826,0.00035242486,0.0025293627],"category_scores_gemma":[0.00012399317,0.00034710614,0.00059778924,0.0004984466,0.00022931093,0.00024573543,0.00022648576,0.0009489151,0.001713607],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00010603747,0.000012452318,0.00007312243,0.00006749929,0.0000038496905,0.00015110151,0.000023930543,0.00022105125,0.9946682,0.00041739867,0.00013943201,0.004116068],"study_design_scores_gemma":[0.00014259663,0.00058517995,0.023616586,0.00007042705,0.00016075314,0.0021641143,0.00013569098,0.0028155765,0.9165828,0.0034279143,0.050241474,0.000056891884],"about_ca_topic_score_codex":0.0014928799,"about_ca_topic_score_gemma":0.0023812028,"teacher_disagreement_score":0.0025293627,"about_ca_system_score_codex":0.000281191,"about_ca_system_score_gemma":0.0004975847,"threshold_uncertainty_score":0.008461535},"labels":[],"label_agreement":null},{"id":"W2095821741","doi":"10.1038/ng.782","title":"A genome-wide association study in Europeans and South Asians identifies five new loci for coronary artery disease","year":2011,"lang":"en","type":"review","venue":"Nature Genetics","topic":"Genetic Associations and Epidemiology","field":"Biochemistry, Genetics and Molecular Biology","cited_by":686,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Hamilton Health Sciences; McGill Genome Centre; Population Health Research Institute; McMaster University; McGill University","funders":"British Heart Foundation; National Institute for Health and Care Research","keywords":"Biology; Locus (genetics); Genome-wide association study; Single-nucleotide polymorphism; Genetics; Genetic association; Coronary artery disease; Expression quantitative trait loci; SNP; Quantitative trait locus; Heritability; Gene; Genotype; Internal medicine; Medicine","score_opus":0.023448480616977477,"score_gpt":0.29664534602970666,"score_spread":0.2731968654127292,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2095821741","genre_codex":"review","genre_gemma":"review","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"review","genre_consensus":"review","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.00022566676,0.99721056,0.00054422294,0.0011332065,0.00028065353,0.0000041535964,0.000045373177,0.000011663702,0.0005445064],"genre_scores_gemma":[0.0010575507,0.9968267,0.0006135021,0.00064395415,0.0003537945,0.000007455856,0.00006836912,0.0000021134053,0.00042649682],"study_design_codex":"design_other","study_design_gemma":"meta_analysis","domain_scores_codex":[0.99956065,0.000076949036,0.00006166917,0.00010916084,0.00015936808,0.000032241463],"domain_scores_gemma":[0.99842274,0.0008948381,0.00015033047,0.000046966088,0.00037237746,0.00011266536],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.002023864,0.0013327802,0.0021533926,0.0015529394,0.0002530157,0.0010877163,0.0013923262,0.0018516214,0.0015380379],"category_scores_gemma":[0.0020834436,0.0003853848,0.00056145707,0.002269217,0.0008602573,0.0010453754,0.00084649114,0.0023107424,0.0012246782],"study_design_candidate":"meta_analysis","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00019544837,0.000056643734,0.0019363661,0.0051085902,0.00031111928,0.00030678223,0.000034793346,0.00020360875,0.0012817886,0.0021428508,0.031099603,0.9573225],"study_design_scores_gemma":[0.00017644721,0.0001624536,0.014306687,0.004922482,0.0009789777,0.0033625877,0.00013973625,0.00020224544,0.0011034932,0.0076877302,0.9668677,0.000089378584],"about_ca_topic_score_codex":0.0022870775,"about_ca_topic_score_gemma":0.0049706176,"teacher_disagreement_score":0.0022870775,"about_ca_system_score_codex":0.0006221211,"about_ca_system_score_gemma":0.0015566049,"threshold_uncertainty_score":0.010703325},"labels":[],"label_agreement":null},{"id":"W2095936660","doi":"10.1038/ng.3185","title":"Identification of six new susceptibility loci for invasive epithelial ovarian cancer","year":2015,"lang":"en","type":"review","venue":"Nature Genetics","topic":"Ovarian cancer diagnosis and treatment","field":"Medicine","cited_by":262,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Canada's Michael Smith Genome Sciences Centre; Princess Margaret Cancer Centre; Lunenfeld-Tanenbaum Research Institute; Mount Sinai Hospital; University Health Network; University of Toronto; Université Laval; BC Cancer Agency; McGill University; Simon Fraser University; Women's College Hospital; Centre hospitalier universitaire de Québec","funders":"National Center for Advancing Translational Sciences; National Cancer Institute; Francis Crick Institute; Cancer Research UK; Wellcome Trust","keywords":"Biology; Identification (biology); Epithelial ovarian cancer; Ovarian cancer; Genetics; Computational biology; Cancer","score_opus":0.05529373860324408,"score_gpt":0.38667156070573094,"score_spread":0.33137782210248684,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2095936660","genre_codex":"review","genre_gemma":"review","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"review","genre_consensus":"review","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.00039094646,0.99814796,0.00029998872,0.00043035293,0.00014026987,0.000004139871,0.000037012356,0.000010117408,0.0005392057],"genre_scores_gemma":[0.0024578408,0.9957425,0.000526171,0.0005102371,0.0002491454,0.000006588183,0.000119442826,0.0000022445752,0.0003858295],"study_design_codex":"design_other","study_design_gemma":"observational","domain_scores_codex":[0.9997266,0.00004530768,0.00005441352,0.00005848595,0.00008648924,0.000028583807],"domain_scores_gemma":[0.999332,0.000395256,0.00011445393,0.000018326673,0.000099171,0.000040792806],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0007491169,0.00091940904,0.0017759968,0.001818536,0.00018398043,0.0009034313,0.0009770693,0.0012363843,0.0021762063],"category_scores_gemma":[0.0012784658,0.0003455751,0.00071974285,0.0013391912,0.00046536274,0.0008254958,0.00076629606,0.0015619461,0.0006572564],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00019103476,0.0000674096,0.0022291902,0.014017836,0.00045639728,0.00085564126,0.000066118264,0.00039572638,0.0034829737,0.0026949751,0.01859305,0.95694965],"study_design_scores_gemma":[0.00023439963,0.0002224137,0.00891131,0.0077735474,0.0024373299,0.0063409577,0.00018209193,0.00031676996,0.002411964,0.006416734,0.9646652,0.000087355074],"about_ca_topic_score_codex":0.0009479455,"about_ca_topic_score_gemma":0.0017116951,"teacher_disagreement_score":0.0021762063,"about_ca_system_score_codex":0.0004230197,"about_ca_system_score_gemma":0.0010769494,"threshold_uncertainty_score":0.0072801113},"labels":[],"label_agreement":null},{"id":"W2096063169","doi":"10.1038/ng1339","title":"Functional variants of OCTN cation transporter genes are associated with Crohn disease","year":2004,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Drug Transport and Resistance Mechanisms","field":"Medicine","cited_by":844,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Hospital for Sick Children; Occupational Cancer Research Centre; Mount Sinai Hospital; Lunenfeld-Tanenbaum Research Institute; St. Michael's Hospital; Alethia Biotherapeutics (Canada); University Health Network; SickKids Foundation; University of Toronto","funders":"National Institutes of Health; University of Toronto; Canadian Arthritis Network; Arthritis Society; Crohn's and Colitis Foundation; Crohn's and Colitis Foundation of Canada; Canadian Institutes of Health Research; Genome Canada","keywords":"Crohn's disease; Biology; Haplotype; Single-nucleotide polymorphism; Genetics; Locus (genetics); Disease; Gene; Genotype; Internal medicine; Medicine","score_opus":0.008877370845087414,"score_gpt":0.22242424390759416,"score_spread":0.21354687306250675,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2096063169","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9971016,0.000454817,0.0009849535,0.0003194652,0.00007492692,0.000012451417,0.0002997691,0.000034230805,0.0007178336],"genre_scores_gemma":[0.9983132,0.0001028505,0.0006858312,0.000099569246,0.00005944225,0.000007803785,0.00019990905,0.000029126633,0.00050231826],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99885666,0.0004078882,0.00020004058,0.00024212022,0.00014952073,0.00014367752],"domain_scores_gemma":[0.99691653,0.0014203504,0.0008899598,0.0001579614,0.00016765538,0.00044750693],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0006271707,0.0016031234,0.0008047406,0.0018599939,0.000994476,0.0008656395,0.0007787944,0.0027586888,0.00581879],"category_scores_gemma":[0.0026221466,0.00043841926,0.0010331785,0.0017014552,0.0010924902,0.00050618674,0.00060947484,0.0015368155,0.00051737524],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.014672348,0.00066813856,0.56763494,0.00034213503,0.002167104,0.06729446,0.0013081781,0.0012616722,0.3262161,0.002591312,0.0015786209,0.014265012],"study_design_scores_gemma":[0.0007165035,0.00096372596,0.8745428,0.00017102672,0.0015219941,0.091915846,0.0007322399,0.0042028762,0.018855536,0.002327873,0.003915976,0.00013357647],"about_ca_topic_score_codex":0.0017585367,"about_ca_topic_score_gemma":0.0013810069,"teacher_disagreement_score":0.00581879,"about_ca_system_score_codex":0.00032941828,"about_ca_system_score_gemma":0.00023991687,"threshold_uncertainty_score":0.019465744},"labels":[],"label_agreement":null},{"id":"W2096920403","doi":"10.1038/ng.2293","title":"Common variation near CDKN1A, POLD3 and SHROOM2 influences colorectal cancer risk","year":2012,"lang":"en","type":"review","venue":"Nature Genetics","topic":"Genetic factors in colorectal cancer","field":"Medicine","cited_by":232,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Lunenfeld-Tanenbaum Research Institute; Mount Sinai Hospital","funders":"National Cancer Institute; Biotechnology and Biological Sciences Research Council; Cancer Research UK; Wellcome Trust","keywords":"Colorectal cancer; Biology; Genetics; Genome-wide association study; Case-control study; Genetic association; Cancer; Internal medicine; Single-nucleotide polymorphism; Gene; Genotype; Medicine","score_opus":0.025379575304467276,"score_gpt":0.3488424161670118,"score_spread":0.3234628408625445,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2096920403","genre_codex":"review","genre_gemma":"review","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"review","genre_consensus":"review","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.0011470718,0.9969975,0.00022654502,0.00064344093,0.00016097711,0.0000027106594,0.000060893803,0.000008391672,0.00075255224],"genre_scores_gemma":[0.007828108,0.9902368,0.00046368563,0.00036421526,0.00026408175,0.000005611319,0.0001214488,0.0000025588183,0.0007134768],"study_design_codex":"design_other","study_design_gemma":"systematic_review","domain_scores_codex":[0.999864,0.000027156664,0.000019203078,0.000039006183,0.000038673006,0.000012006233],"domain_scores_gemma":[0.999706,0.00017162038,0.00005334393,0.000007096331,0.000041550833,0.000020308898],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0003893495,0.00050758186,0.0008881582,0.0007775086,0.000120114484,0.00039216198,0.0004508993,0.0006636338,0.0020068428],"category_scores_gemma":[0.0008017646,0.00017561826,0.00042370154,0.0010861683,0.0002603187,0.00031619144,0.00030583752,0.0006853784,0.0004594329],"study_design_candidate":"systematic_review","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00031960293,0.000043256357,0.006456252,0.009916405,0.00072271744,0.0008282378,0.00004392188,0.00053468725,0.0037173491,0.0020239174,0.016446697,0.95894706],"study_design_scores_gemma":[0.00015611883,0.00019456354,0.034554236,0.0047675213,0.0027059051,0.007273631,0.00015183378,0.0004017892,0.0026379032,0.00476082,0.9423288,0.00006688402],"about_ca_topic_score_codex":0.0020347114,"about_ca_topic_score_gemma":0.003409106,"teacher_disagreement_score":0.0020347114,"about_ca_system_score_codex":0.00039168654,"about_ca_system_score_gemma":0.0006797104,"threshold_uncertainty_score":0.0067135096},"labels":[],"label_agreement":null},{"id":"W2097572487","doi":"10.1038/ng.2480","title":"Large-scale association analysis identifies new risk loci for coronary artery disease","year":2012,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Genetic Associations and Epidemiology","field":"Biochemistry, Genetics and Molecular Biology","cited_by":1669,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"McGill University; University of Ottawa","funders":"National Institute of Diabetes and Digestive and Kidney Diseases; Medical Research Council; National Heart, Lung, and Blood Institute; Terveyden ja hyvinvoinnin laitos; Université de Toulouse; Queen's University; Centre for Public Health, Queen's University Belfast; Università degli Studi di Milano-Bicocca; Université Pierre et Marie Curie; Queen's University Belfast; Université de Strasbourg; Institut National de la Santé et de la Recherche Médicale; University of Oxford; National Institute for Health and Care Research; British Heart Foundation; Wellcome Trust; University of Bern","keywords":"Biology; Genome-wide association study; Coronary artery disease; Genetic association; Single-nucleotide polymorphism; Genetics; CAD; Missing heritability problem; Candidate gene; Heritability; Disease; Bioinformatics; Gene; Internal medicine; Medicine; Genotype","score_opus":0.0072031778844167185,"score_gpt":0.26959503005373225,"score_spread":0.26239185216931554,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2097572487","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.98285496,0.002062991,0.01188284,0.00075874676,0.00009772375,0.000024047975,0.000731877,0.00017967484,0.00140711],"genre_scores_gemma":[0.9923987,0.00049736095,0.005424245,0.00018184735,0.00012444417,0.000022384538,0.0006089802,0.000058439327,0.00068366097],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99802965,0.0009720423,0.000116982286,0.0005254511,0.00025908946,0.000096729935],"domain_scores_gemma":[0.9924678,0.0045038955,0.00095254584,0.0011817623,0.0003909876,0.00050302554],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0032105884,0.00058556366,0.0006859354,0.0015083753,0.0007021547,0.0012735176,0.0007549853,0.00080465653,0.0024431369],"category_scores_gemma":[0.006678383,0.0004830532,0.00083850016,0.001970812,0.00079188123,0.0005512231,0.00082410115,0.0012704022,0.00044050356],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.002771091,0.0004450542,0.8903472,0.00015301703,0.0029470467,0.0013798989,0.000301935,0.0009475855,0.063307874,0.0009814659,0.0020075238,0.03441037],"study_design_scores_gemma":[0.00013419229,0.00014696777,0.9906495,0.000010323167,0.000750274,0.0011603301,0.00011709427,0.0019552442,0.002011477,0.0016442289,0.001392918,0.000027422271],"about_ca_topic_score_codex":0.0013125113,"about_ca_topic_score_gemma":0.002760266,"teacher_disagreement_score":0.0032105884,"about_ca_system_score_codex":0.00019432929,"about_ca_system_score_gemma":0.00034143124,"threshold_uncertainty_score":0.016979396},"labels":[],"label_agreement":null},{"id":"W2097804771","doi":"10.1038/ng.952","title":"Deep resequencing of GWAS loci identifies independent rare variants associated with inflammatory bowel disease","year":2011,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Inflammatory Bowel Disease","field":"Biochemistry, Genetics and Molecular Biology","cited_by":785,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Toronto; Mount Sinai Hospital; Université de Montréal; Montreal Heart Institute","funders":"National Center for Research Resources; National Human Genome Research Institute; Canadian Institutes of Health Research; National Institutes of Health; National Institute of Allergy and Infectious Diseases; Institut de Cardiologie de Montréal; Exzellenzclusters Entzündungsforschung; Vetenskapsrådet; Crohn's and Colitis UK; Leona M. and Harry B. Helmsley Charitable Trust; Örebro Universitet; Cedars-Sinai Medical Center; Deutsche Forschungsgemeinschaft; National Institute of Diabetes and Digestive and Kidney Diseases; Crohn's and Colitis Foundation of Canada; Universitetssjukhuset Örebro; Broad Institute; Crohn's and Colitis Foundation; Crohn's and Colitis Foundation of America","keywords":"Genome-wide association study; Biology; Inflammatory bowel disease; Genotyping; Genetics; Genetic association; PTPN22; Odds ratio; Disease; Case-control study; NOD2; Single-nucleotide polymorphism; Gene; Genotype; Medicine; Internal medicine","score_opus":0.008528298562396336,"score_gpt":0.22426492137369738,"score_spread":0.21573662281130104,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2097804771","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9898211,0.00040921548,0.0069514797,0.00016147745,0.000046254667,0.000027028269,0.0014246476,0.00008587895,0.0010729632],"genre_scores_gemma":[0.99365413,0.0001346803,0.0037503862,0.00019242195,0.000037501803,0.000018569379,0.0014836566,0.000052941024,0.00067564304],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9993217,0.00014672511,0.00005969065,0.00019637022,0.00015328373,0.00012216732],"domain_scores_gemma":[0.9987062,0.0007476614,0.00017815137,0.00017876967,0.000066516484,0.00012264137],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.000926046,0.0004542324,0.00067567284,0.0013689435,0.0005826295,0.0010137826,0.00044157525,0.00069692044,0.0016031396],"category_scores_gemma":[0.0018649927,0.0004170889,0.00095176,0.0008355938,0.0004303591,0.00017428125,0.0006861976,0.0010355021,0.00035579666],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0036892819,0.00031402288,0.21257308,0.00020625394,0.0020658928,0.003454143,0.000611838,0.004254183,0.7137375,0.0028837903,0.002149355,0.054060675],"study_design_scores_gemma":[0.00051640056,0.00052837975,0.91031337,0.00008218811,0.001967052,0.004624383,0.00027006253,0.01942013,0.047839012,0.0053466936,0.008969354,0.00012299094],"about_ca_topic_score_codex":0.0015156997,"about_ca_topic_score_gemma":0.0056992536,"teacher_disagreement_score":0.0016031396,"about_ca_system_score_codex":0.00025630707,"about_ca_system_score_gemma":0.00029749522,"threshold_uncertainty_score":0.0053629875},"labels":[],"label_agreement":null},{"id":"W2098189071","doi":"10.1038/ng1001-166","title":"A gene encoding a putative GTPase regulator is mutated in familial amyotrophic lateral sclerosis 2","year":2001,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Amyotrophic Lateral Sclerosis Research","field":"Medicine","cited_by":676,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of British Columbia; Hospital for Sick Children; Children's & Women's Health Centre of British Columbia; McGill University; University of Ottawa; Montreal General Hospital","funders":"","keywords":"Biology; Genetics; Amyotrophic lateral sclerosis; Gene; Exon; Mutation; Coding region; Homology (biology)","score_opus":0.03055374119248361,"score_gpt":0.30738760994673486,"score_spread":0.27683386875425126,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2098189071","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9929455,0.00073674956,0.0017763794,0.00038075246,0.000208153,0.000039408893,0.0004874191,0.00016906232,0.0032565591],"genre_scores_gemma":[0.9953577,0.00021671053,0.0013414894,0.00015011629,0.00007653252,0.000030368792,0.00060796406,0.000039391165,0.0021798115],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.99979895,0.000031796317,0.000029155688,0.000058079804,0.000049295733,0.000032646716],"domain_scores_gemma":[0.99959236,0.00016550325,0.000087404514,0.000022860944,0.000031299878,0.00010052305],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00023874444,0.0012200384,0.000644836,0.0012387016,0.0009737845,0.0006644939,0.0006728035,0.0021537696,0.0030365025],"category_scores_gemma":[0.00084410334,0.00028343927,0.0007405173,0.0005168161,0.0006454484,0.0004099784,0.0005975569,0.0006719163,0.001134477],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0019121551,0.00023859668,0.010619523,0.00022355036,0.00013287354,0.16465425,0.00081962766,0.0008037293,0.80814475,0.0024541612,0.0016646737,0.008332148],"study_design_scores_gemma":[0.0008436629,0.0014463775,0.14901154,0.00018739475,0.0006902917,0.33733776,0.0013673676,0.01084662,0.46160966,0.0039925096,0.032454517,0.0002123572],"about_ca_topic_score_codex":0.0011000863,"about_ca_topic_score_gemma":0.0005526056,"teacher_disagreement_score":0.0030365025,"about_ca_system_score_codex":0.00048039656,"about_ca_system_score_gemma":0.0003127932,"threshold_uncertainty_score":0.010158122},"labels":[],"label_agreement":null},{"id":"W2099220382","doi":"10.1038/ng1963","title":"Protein tyrosine phosphatase 1B deficiency or inhibition delays ErbB2-induced mammary tumorigenesis and protects from lung metastasis","year":2007,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Protein Tyrosine Phosphatases","field":"Biochemistry, Genetics and Molecular Biology","cited_by":320,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Royal Victoria Hospital; McGill University; Royal Victoria Regional Health Centre; Merck Canada Inc. (Canada); McGill University Health Centre","funders":"","keywords":"Biology; Carcinogenesis; Cancer research; Metastasis; Protein tyrosine phosphatase; Mammary gland; Protein kinase B; Genetically modified mouse; Mammary tumor; MAPK/ERK pathway; Receptor tyrosine kinase; Transgene; Breast cancer; Cancer; Signal transduction; Cell biology; Genetics; Gene","score_opus":0.009424190743949783,"score_gpt":0.25752513567677227,"score_spread":0.24810094493282248,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2099220382","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.98823535,0.0031118777,0.0031882373,0.0005849083,0.00024836767,0.000044732384,0.0013278894,0.000654813,0.0026038873],"genre_scores_gemma":[0.98705184,0.0012648149,0.0012265415,0.00009269663,0.00003112348,0.000052184387,0.0009996672,0.00011893609,0.009162109],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9997172,0.00003315154,0.000021221498,0.000054386957,0.00006483567,0.00010923126],"domain_scores_gemma":[0.9995666,0.00006348252,0.000108342465,0.000056917634,0.00002289042,0.0001817954],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00024328203,0.0008381723,0.0007187798,0.0008446303,0.00033576443,0.000688466,0.0007611344,0.0006218019,0.0039647757],"category_scores_gemma":[0.00023515352,0.0006597938,0.00047846962,0.00037590397,0.0005649474,0.00055070245,0.00037092777,0.002054297,0.0009928874],"study_design_candidate":"bench_or_experimental","study_design_consensus":"bench_or_experimental","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00072944706,0.0001222946,0.00015686563,0.000027874206,0.000012474549,0.000058788664,0.000009927989,0.0001246994,0.99687356,0.00027763064,0.00018691074,0.0014196433],"study_design_scores_gemma":[0.00011463157,0.00072363834,0.0026191052,0.00000781473,0.000029744724,0.00032689364,0.000041759904,0.0009930725,0.99264055,0.00015189085,0.0023399354,0.000010938435],"about_ca_topic_score_codex":0.002438146,"about_ca_topic_score_gemma":0.0033174155,"teacher_disagreement_score":0.0039647757,"about_ca_system_score_codex":0.00074869185,"about_ca_system_score_gemma":0.00076789554,"threshold_uncertainty_score":0.013263524},"labels":[],"label_agreement":null},{"id":"W2099326239","doi":"10.1038/ng.2568","title":"Sequencing of the sea lamprey (Petromyzon marinus) genome provides insights into vertebrate evolution","year":2013,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Genomics and Phylogenetic Studies","field":"Biochemistry, Genetics and Molecular Biology","cited_by":652,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Sunnybrook Health Science Centre; University of Toronto","funders":"Eunice Kennedy Shriver National Institute of Child Health and Human Development; National Center for Research Resources; National Institute of Dental and Craniofacial Research; National Science Foundation; University of Washington; Canadian Institutes of Health Research; College of Engineering, Michigan State University; New Hampshire Agricultural Experiment Station; Natural Sciences and Engineering Research Council of Canada; National Human Genome Research Institute; Wellcome Trust; U.S. Geological Survey; Stowers Institute for Medical Research; National Institute of Neurological Disorders and Stroke; National Institute of General Medical Sciences; University of Utah; Michigan State University; National Institutes of Health","keywords":"Lamprey; Biology; Vertebrate; Petromyzon; Genome; Evolutionary biology; Lineage (genetic); Phylum; Phylogenetics; Extant taxon; Genetics; Gene; Paleontology","score_opus":0.005219701527135528,"score_gpt":0.20113107156681695,"score_spread":0.19591137003968143,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2099326239","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9128245,0.021823723,0.025226582,0.0067059495,0.000927021,0.00010932039,0.019762894,0.0017906013,0.01082942],"genre_scores_gemma":[0.86890787,0.022310194,0.054984026,0.0027838743,0.0004091285,0.000086621956,0.0322097,0.00050181756,0.017806755],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9998822,0.000007775346,0.000008677152,0.00004386906,0.000039397917,0.000017929238],"domain_scores_gemma":[0.9996418,0.00004734585,0.000062145504,0.000035111138,0.00014023912,0.0000732895],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0002608133,0.00039829867,0.0003287682,0.0007295374,0.00040620312,0.000647939,0.00022150612,0.0005921261,0.0014368156],"category_scores_gemma":[0.0004934281,0.00025178047,0.00045127576,0.00058049103,0.00022178974,0.00040457194,0.00042965834,0.00087888073,0.0009803496],"study_design_candidate":"bench_or_experimental","study_design_consensus":"bench_or_experimental","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00033138908,0.000040748164,0.01412507,0.00055170525,0.0001333793,0.0004612775,0.0004295124,0.00073341344,0.9030356,0.0012312921,0.0074069942,0.07151966],"study_design_scores_gemma":[0.00006563819,0.00032525984,0.34092554,0.00034421435,0.00061873405,0.001579821,0.0009933454,0.005438147,0.2969082,0.0042956644,0.34837753,0.0001279727],"about_ca_topic_score_codex":0.0066558067,"about_ca_topic_score_gemma":0.0135249775,"teacher_disagreement_score":0.0066558067,"about_ca_system_score_codex":0.0006344722,"about_ca_system_score_gemma":0.00070219586,"threshold_uncertainty_score":0.0132341385},"labels":[],"label_agreement":null},{"id":"W2099598799","doi":"10.1038/ng.941","title":"Genome-wide association and large-scale follow up identifies 16 new loci influencing lung function","year":2011,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Chronic Obstructive Pulmonary Disease (COPD) Research","field":"Medicine","cited_by":416,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Lunenfeld-Tanenbaum Research Institute; Ontario Institute for Cancer Research; Memorial University of Newfoundland","funders":"National Institute of Child Health and Human Development; National Institute of Environmental Health Sciences; National Institute of Neurological Disorders and Stroke; National Institute of Diabetes and Digestive and Kidney Diseases; National Institute of Allergy and Infectious Diseases; National Human Genome Research Institute; National Institute of Mental Health; National Institute on Aging; Münchner Zentrum für Gesundheitswissenschaften; Helmholtz Zentrum München; Tartu Ülikool; Medical Research Council; Canadian Cancer Society Research Institute; National Institutes of Health; Hjartavernd; Healthway; Tays; Novo Nordisk Fonden; AstraZeneca; European Commission; International Osteoporosis Foundation; Sydäntutkimussäätiö; Universitair Medisch Centrum Groningen; Asthma and Lung UK; Vetenskapsrådet; Nederlandse Organisatie voor Wetenschappelijk Onderzoek; East Midlands Development Agency; Novo Nordisk; Cambridge University Hospitals; British Heart Foundation; Bundesministerium für Bildung und Forschung; University of Cambridge; ZonMw; National Health and Medical Research Council; Oulun Yliopisto; Schweizerischer Nationalfonds zur Förderung der Wissenschaftlichen Forschung; Royal Society; University of Leicester; Erasmus Medisch Centrum; National Science Foundation; British Lung Foundation; National Heart, Lung, and Blood Institute; Biotechnology and Biological Sciences Research Council; National Cancer Institute; AXA Research Fund; Cancer Research UK; Wellcome Trust; Norges Teknisk-Naturvitenskapelige Universitet; European Regional Development Fund; King's College London; Jalmari ja Rauha Ahokkaan Säätiö; U.S. Public Health Service; Foundation for Cardiovascular Research; National Eye Institute; Biocenter, University of Oulu; National Institute for Health and Care Research; Flight Attendant Medical Research Institute; National Center for Research Resources; Nierstichting; University of Bristol; Directorate for Biological Sciences; GlaxoSmithKline; Canadian Institutes of Health Research; Juvenile Diabetes Research Foundation International","keywords":"Genome-wide association study; Pulmonary function testing; Vital capacity; Biology; Airway obstruction; Lung; Lung function; Genetics; Bioinformatics; Internal medicine; Medicine; Single-nucleotide polymorphism; Genotype; Airway; Gene; Diffusing capacity","score_opus":0.011943033026910781,"score_gpt":0.2637124933437815,"score_spread":0.2517694603168707,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2099598799","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99750996,0.0005429924,0.0008764794,0.00016505359,0.000021659902,0.000008816347,0.00051407935,0.000021991893,0.0003390304],"genre_scores_gemma":[0.99829906,0.0001484448,0.00066145003,0.000060804552,0.000024682875,0.000013385055,0.00039585924,0.0000138771675,0.00038260478],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9992574,0.00020553426,0.00006049575,0.00027990245,0.00009244351,0.000104166844],"domain_scores_gemma":[0.99815935,0.00094419805,0.0003764363,0.0002250236,0.00009580546,0.00019915235],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0009449237,0.0006141935,0.0006434221,0.0010095633,0.0006895485,0.000872181,0.00076995115,0.001179696,0.0018493843],"category_scores_gemma":[0.0020598304,0.0003609338,0.0011098228,0.0018091999,0.00053301116,0.0003201978,0.00050121295,0.000981305,0.00029093536],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0027995906,0.00025095738,0.94293565,0.000050901424,0.0009184,0.0015918183,0.00036692148,0.00039634734,0.034164663,0.00016894353,0.00056240335,0.015793554],"study_design_scores_gemma":[0.0000768739,0.00014641971,0.9965125,0.0000051429556,0.00030421268,0.0008170418,0.00008205533,0.00035832624,0.0010027139,0.00021989239,0.0004635755,0.000011260083],"about_ca_topic_score_codex":0.003088021,"about_ca_topic_score_gemma":0.0037141647,"teacher_disagreement_score":0.003088021,"about_ca_system_score_codex":0.00023285527,"about_ca_system_score_gemma":0.00029632752,"threshold_uncertainty_score":0.0061867833},"labels":[],"label_agreement":null},{"id":"W2099701757","doi":"10.1038/ng2114","title":"The imprinted gene Magel2 regulates normal circadian output","year":2007,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":225,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Alberta","funders":"National Eye Institute; National Institute of Mental Health; National Institutes of Health","keywords":"Circadian rhythm; Biology; Suprachiasmatic nucleus; Orexin; Endocrinology; Internal medicine; Orexin-A; Hypothalamus; Phenotype; Gene; CLOCK; Cell biology; Circadian clock; Genetics; Neuropeptide; Medicine; Receptor","score_opus":0.0051499725056270125,"score_gpt":0.2351019312492238,"score_spread":0.22995195874359678,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2099701757","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9792758,0.0030316198,0.012250692,0.00034432078,0.00020156133,0.000012328701,0.00051403575,0.00048528702,0.0038843295],"genre_scores_gemma":[0.9959811,0.00040203502,0.0014172398,0.000038327216,0.000018203491,0.0000069138464,0.00017374523,0.000060836537,0.0019015627],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9998976,0.000013537148,0.0000053313693,0.000025275724,0.000028584773,0.00002966269],"domain_scores_gemma":[0.9998313,0.00002701124,0.00004571845,0.000021044922,0.000017674005,0.000057166377],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00010787095,0.0004251887,0.00018125834,0.0004278441,0.0001936885,0.00046280056,0.00034272939,0.00029165103,0.0008603234],"category_scores_gemma":[0.00026195447,0.0002314517,0.0001577407,0.00015567122,0.00034828568,0.00027599258,0.00046886946,0.00041427166,0.00027372193],"study_design_candidate":"bench_or_experimental","study_design_consensus":"bench_or_experimental","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00018762313,0.0000043410078,0.00089293724,0.00001245529,0.000005562913,0.00030308065,0.000013871367,0.00015607952,0.9954646,0.0008743983,0.000113448084,0.0019715582],"study_design_scores_gemma":[0.000021438866,0.000043199256,0.020367788,0.0000038960243,0.000014964056,0.00092759065,0.00003524815,0.0017966917,0.97230613,0.00060935016,0.0038623468,0.000011414973],"about_ca_topic_score_codex":0.00068306935,"about_ca_topic_score_gemma":0.0012330125,"teacher_disagreement_score":0.0008603234,"about_ca_system_score_codex":0.00055419985,"about_ca_system_score_gemma":0.00025169837,"threshold_uncertainty_score":0.0040210485},"labels":[],"label_agreement":null},{"id":"W2100024496","doi":"10.1038/ng.3221","title":"Analysis of the genetic phylogeny of multifocal prostate cancer identifies multiple independent clonal expansions in neoplastic and morphologically normal prostate tissue","year":2015,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Cancer Genomics and Diagnostics","field":"Biochemistry, Genetics and Molecular Biology","cited_by":457,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Princess Margaret Cancer Centre; Ontario Institute for Cancer Research; University of Toronto; University Health Network","funders":"Biotechnology and Biological Sciences Research Council; Vlaamse regering; Wellcome Trust; Hutchison Whampoa Limited; Fonds Wetenschappelijk Onderzoek; Rosetrees Trust; National Institute for Health and Care Research; Cambridge University Hospitals; North West Cancer Research; Royal Marsden NHS Foundation Trust; Francis Crick Institute; University of Cambridge; Cancer Research UK","keywords":"Biology; Prostate cancer; Cancer; Carcinogenesis; Somatic evolution in cancer; Prostate; Chromothripsis; Genetics; Pathology; DNA; Genome instability; DNA damage","score_opus":0.007907214586845568,"score_gpt":0.2565585614107501,"score_spread":0.24865134682390455,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2100024496","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9982412,0.00015790905,0.0011141186,0.000017031209,0.0000010733027,0.000004359725,0.000078624704,0.000016598015,0.00036915127],"genre_scores_gemma":[0.9980672,0.000080991435,0.0013859431,0.0000118781545,0.0000017821625,0.0000049386676,0.00017109494,0.000011705538,0.00026446106],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.99989104,0.000013524749,0.000005022885,0.000026414948,0.0000353838,0.00002856044],"domain_scores_gemma":[0.99959594,0.00015940244,0.00008628015,0.00003228697,0.000065931905,0.000060262384],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00018986038,0.00008220017,0.00012569106,0.0008031107,0.00022250206,0.0002902635,0.00017615291,0.00018917983,0.0008058532],"category_scores_gemma":[0.00046263338,0.00014009512,0.00012301312,0.00033735184,0.00018802265,0.00014485588,0.00028475077,0.00031810568,0.00014088348],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0002003528,0.000014767827,0.03952501,0.000023752322,0.0000144697115,0.00012711501,0.00012866639,0.00048190422,0.9520549,0.00036892205,0.000045592085,0.0070146844],"study_design_scores_gemma":[0.00001677248,0.00021026861,0.8751378,0.000011032964,0.000058216396,0.0026960804,0.00021685413,0.008265878,0.11038208,0.0005334455,0.0024560126,0.00001547942],"about_ca_topic_score_codex":0.0012942534,"about_ca_topic_score_gemma":0.0026584363,"teacher_disagreement_score":0.0012942534,"about_ca_system_score_codex":0.00027994902,"about_ca_system_score_gemma":0.00014423786,"threshold_uncertainty_score":0.0026958585},"labels":[],"label_agreement":null},{"id":"W2101259235","doi":"10.1038/ng1598","title":"Chromosome-wide and promoter-specific analyses identify sites of differential DNA methylation in normal and transformed human cells","year":2005,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Epigenetics and DNA Methylation","field":"Biochemistry, Genetics and Molecular Biology","cited_by":1754,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"BC Cancer Agency","funders":"","keywords":"Biology; DNA methylation; CpG site; Epigenetics; Methylation; Promoter; Differentially methylated regions; Epigenetics of physical exercise; Genetics; Illumina Methylation Assay; RNA-Directed DNA Methylation; Gene; Human genome; Molecular biology; Epigenomics; Chromosome; Genome; Gene expression","score_opus":0.018116983720515758,"score_gpt":0.3116644724781628,"score_spread":0.2935474887576471,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2101259235","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99471635,0.0012560722,0.0021915354,0.000081879705,0.000011237934,0.0000090141875,0.0008775025,0.0000677921,0.00078857027],"genre_scores_gemma":[0.9963152,0.00050910306,0.00067540014,0.00003245162,0.0000057089364,0.000014755133,0.0011394112,0.000023957988,0.0012839861],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.99988425,0.000012493551,0.000007434515,0.000035879195,0.000031821175,0.000028140425],"domain_scores_gemma":[0.9998405,0.000061423794,0.000023974617,0.000021633603,0.00002096075,0.000031478776],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00011270309,0.00014967476,0.0003085689,0.00061826746,0.00024507442,0.0003924641,0.00022725452,0.00027515055,0.0019294398],"category_scores_gemma":[0.00028193512,0.000285917,0.00024900545,0.00042132862,0.00030724588,0.00012542575,0.0002480569,0.00048491816,0.00043246037],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0004904205,0.000015610445,0.0038753408,0.000025666975,0.000026265276,0.00006716303,0.00009160613,0.00008006001,0.9930467,0.00018062924,0.000058254504,0.0020423012],"study_design_scores_gemma":[0.00007616255,0.00034901616,0.23223199,0.000005752004,0.00012359644,0.0021365013,0.00021782171,0.0014239702,0.7596664,0.000516744,0.0032342195,0.000017816916],"about_ca_topic_score_codex":0.0023707536,"about_ca_topic_score_gemma":0.0029121325,"teacher_disagreement_score":0.0023707536,"about_ca_system_score_codex":0.00022958113,"about_ca_system_score_gemma":0.0001574097,"threshold_uncertainty_score":0.006454587},"labels":[],"label_agreement":null},{"id":"W2101486850","doi":"10.1038/ng.2627","title":"Genome-wide association analyses in Han Chinese identify two new susceptibility loci for amyotrophic lateral sclerosis","year":2013,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Amyotrophic Lateral Sclerosis Research","field":"Medicine","cited_by":72,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Occupational Cancer Research Centre; University of Toronto","funders":"","keywords":"Genome-wide association study; Biology; Single-nucleotide polymorphism; Amyotrophic lateral sclerosis; Genetics; Genetic association; Odds ratio; Genetic predisposition; Disease; Gene; Genotype; Medicine; Internal medicine","score_opus":0.04149046595433079,"score_gpt":0.36644176030453957,"score_spread":0.32495129435020875,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2101486850","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9988594,0.00018289634,0.00034828036,0.00007935375,0.000010441847,0.0000064433866,0.00011599684,0.00000865331,0.0003884865],"genre_scores_gemma":[0.9989384,0.000078965255,0.00037790963,0.000044473825,0.000016249032,0.0000073295682,0.000117972384,0.0000060695966,0.00041278297],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99971837,0.000052296855,0.000030102985,0.00007936104,0.000055796263,0.000064001004],"domain_scores_gemma":[0.99922514,0.00033712908,0.00014729584,0.00006188763,0.00007097564,0.00015753543],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0005675071,0.00063067186,0.0004400612,0.0014932582,0.0009077741,0.0004954913,0.0006119451,0.0005638457,0.002068398],"category_scores_gemma":[0.0011205758,0.00029851662,0.000874987,0.0013807544,0.00053026713,0.00018925579,0.0003859994,0.00046105924,0.0001898269],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0046946937,0.00037863542,0.8460405,0.00011329846,0.0011255263,0.009301941,0.002340075,0.00045311433,0.11563177,0.00090525474,0.0007142296,0.018301038],"study_design_scores_gemma":[0.00013142018,0.00013057752,0.9930368,0.000007599001,0.00040881237,0.0015402036,0.00030119205,0.0005724529,0.0030479257,0.00034014988,0.00046287436,0.00002004093],"about_ca_topic_score_codex":0.0126789985,"about_ca_topic_score_gemma":0.01635498,"teacher_disagreement_score":0.0126789985,"about_ca_system_score_codex":0.00038370508,"about_ca_system_score_gemma":0.00059664034,"threshold_uncertainty_score":0.02521044},"labels":[],"label_agreement":null},{"id":"W2101794801","doi":"10.1038/ng.3118","title":"Discovery of new risk loci for IgA nephropathy implicates genes involved in immunity against intestinal pathogens","year":2014,"lang":"en","type":"review","venue":"Nature Genetics","topic":"Renal Diseases and Glomerulopathies","field":"Medicine","cited_by":626,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Calgary","funders":"National Institute of Diabetes and Digestive and Kidney Diseases; National Center for Advancing Translational Sciences; Howard Hughes Medical Institute","keywords":"Biology; Genome-wide association study; Nephropathy; Human leukocyte antigen; Allele; Single-nucleotide polymorphism; Genetics; Disease; Immunology; Locus (genetics); Genetic variation; Genetic association; Gene; Genotype; Diabetes mellitus; Antigen","score_opus":0.025776206097023566,"score_gpt":0.3241589730187773,"score_spread":0.2983827669217537,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2101794801","genre_codex":"review","genre_gemma":"review","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"review","genre_consensus":"review","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.00039804808,0.9976956,0.00036043942,0.00065299997,0.00019252166,0.000003179787,0.000034626395,0.000011892477,0.00065071683],"genre_scores_gemma":[0.0018494537,0.99646425,0.00043932482,0.0004122388,0.0003220201,0.00000398759,0.00006423766,0.0000018468794,0.00044260392],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.9998306,0.000026183767,0.000025255935,0.000036296442,0.00006304919,0.00001853406],"domain_scores_gemma":[0.99954873,0.00025600768,0.000061036124,0.000011302732,0.00008125031,0.000041699222],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0006030058,0.00090577826,0.0013322161,0.001508015,0.00015635687,0.00070272305,0.00080056133,0.0011566338,0.0019357143],"category_scores_gemma":[0.00074325583,0.00018647399,0.0004898109,0.0013141042,0.00041361662,0.00060898735,0.00056740927,0.0013066622,0.0005833021],"study_design_candidate":"not_applicable","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00018056265,0.000052990985,0.0014460166,0.008493801,0.0002979977,0.0007727166,0.00004091695,0.00035793163,0.003839059,0.0027168528,0.023909431,0.95789176],"study_design_scores_gemma":[0.000088390254,0.00008957164,0.005032592,0.0037751172,0.0008336488,0.0042645503,0.00009569888,0.00021143908,0.0014224064,0.004080166,0.9800646,0.00004181117],"about_ca_topic_score_codex":0.0009038825,"about_ca_topic_score_gemma":0.0014981527,"teacher_disagreement_score":0.0019357143,"about_ca_system_score_codex":0.00039762096,"about_ca_system_score_gemma":0.0008505888,"threshold_uncertainty_score":0.0064756274},"labels":[],"label_agreement":null},{"id":"W2102413929","doi":"10.1038/ng.522","title":"A genome-wide association study identifies pancreatic cancer susceptibility loci on chromosomes 13q22.1, 1q32.1 and 5p15.33","year":2010,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Pancreatic and Hepatic Oncology Research","field":"Medicine","cited_by":614,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Toronto; Lunenfeld-Tanenbaum Research Institute; Cancer Care Ontario; Mount Sinai Hospital","funders":"National Cancer Institute; National Institutes of Health; Mayo Clinic","keywords":"Single-nucleotide polymorphism; Biology; Locus (genetics); Genetics; Allele; Genome-wide association study; Genotype; Odds ratio; SNP; Pancreatic cancer; Internal medicine; Cancer; Gene; Medicine","score_opus":0.016126636543903155,"score_gpt":0.3442386196704849,"score_spread":0.32811198312658174,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2102413929","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9917862,0.001770742,0.002657195,0.00074329635,0.00006109838,0.000039900824,0.001328299,0.00009331016,0.0015199047],"genre_scores_gemma":[0.9958852,0.00049341767,0.0014865691,0.00016303467,0.00003436275,0.000032073953,0.00096298347,0.000018878573,0.0009234622],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9994344,0.00013048426,0.000035732643,0.00018495123,0.000119833785,0.00009452947],"domain_scores_gemma":[0.9986743,0.0005751416,0.00032151473,0.00009786633,0.000085866086,0.00024529954],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00086374115,0.0007623985,0.0005345474,0.001684965,0.0007616379,0.00072108366,0.00078194967,0.0008128347,0.005230603],"category_scores_gemma":[0.00239025,0.00042254713,0.001058133,0.0019320817,0.00049730425,0.00020560474,0.00086487975,0.0011822196,0.00038107517],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0047887694,0.0004184244,0.8741286,0.00020024156,0.0025799188,0.007530131,0.0004544131,0.00096706505,0.06733706,0.00079407316,0.0047585587,0.03604264],"study_design_scores_gemma":[0.00028721694,0.0003179102,0.9850786,0.000042020507,0.001016747,0.0045013484,0.00014325099,0.00096034165,0.004208002,0.00053927494,0.0028790378,0.00002630469],"about_ca_topic_score_codex":0.007332632,"about_ca_topic_score_gemma":0.0130298445,"teacher_disagreement_score":0.007332632,"about_ca_system_score_codex":0.00033425883,"about_ca_system_score_gemma":0.00043949822,"threshold_uncertainty_score":0.017498136},"labels":[],"label_agreement":null},{"id":"W2102889851","doi":"10.1038/ng.2467","title":"Identification of 15 new psoriasis susceptibility loci highlights the role of innate immunity","year":2012,"lang":"en","type":"review","venue":"Nature Genetics","topic":"Psoriasis: Treatment and Pathogenesis","field":"Immunology and Microbiology","cited_by":1047,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Memorial University of Newfoundland; Toronto Western Hospital; University of Toronto; Centre for Addiction and Mental Health","funders":"Eunice Kennedy Shriver National Institute of Child Health and Human Development; National Institute of Arthritis and Musculoskeletal and Skin Diseases; National Human Genome Research Institute; National Institute for Health and Care Research; Canadian Institutes of Health Research; Versus Arthritis; Medical Research Council; Wellcome Trust","keywords":"Biology; Genome-wide association study; Innate immune system; Psoriasis; Genetics; Candidate gene; Genetic architecture; Immunology; Immune system; Gene; Computational biology; Phenotype; Single-nucleotide polymorphism; Genotype","score_opus":0.022818241077731772,"score_gpt":0.2848450931229573,"score_spread":0.2620268520452255,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2102889851","genre_codex":"review","genre_gemma":"review","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"review","genre_consensus":"review","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.00036716214,0.9972626,0.00058006984,0.00063499075,0.00028306054,0.000004144487,0.000032062373,0.000021158958,0.0008147534],"genre_scores_gemma":[0.001984673,0.9949826,0.00077489717,0.0006673565,0.00060375413,0.000007784212,0.00010550944,0.00000462093,0.0008687769],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.9997855,0.000026200494,0.00003145502,0.0000525889,0.00007999739,0.000024322462],"domain_scores_gemma":[0.9995448,0.00019247351,0.00007702969,0.000016887274,0.000112709065,0.00005610285],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00066055416,0.00095286925,0.0015543752,0.0013502976,0.00018910065,0.0011014794,0.0008963818,0.001284006,0.0026062129],"category_scores_gemma":[0.00065537554,0.0002531991,0.0005023384,0.0012125145,0.00054023066,0.0009432687,0.0006377347,0.002030241,0.0015726546],"study_design_candidate":"not_applicable","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00013850961,0.000057144378,0.0005052262,0.004600606,0.00008152047,0.0005045232,0.000023581566,0.0002357807,0.0070809633,0.0021220709,0.020176204,0.9644739],"study_design_scores_gemma":[0.00007501253,0.0001693685,0.0028760743,0.0020124395,0.0003377522,0.0049050343,0.000059916754,0.00018847037,0.0037533357,0.0037064976,0.98186815,0.000047983343],"about_ca_topic_score_codex":0.0006848488,"about_ca_topic_score_gemma":0.0011692602,"teacher_disagreement_score":0.0026062129,"about_ca_system_score_codex":0.00059994456,"about_ca_system_score_gemma":0.00091388496,"threshold_uncertainty_score":0.008718669},"labels":[],"label_agreement":null},{"id":"W2103703726","doi":"10.1038/ng1131","title":"Loss of neuropathy target esterase in mice links organophosphate exposure to hyperactivity","year":2003,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Pesticide Exposure and Toxicity","field":"Agricultural and Biological Sciences","cited_by":176,"is_retracted":false,"has_abstract":false,"route_ca_aff":false,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"","funders":"Canadian Institutes of Health Research; National Institutes of Health; U.S. Department of Defense","keywords":"Organophosphate; Biology; Carboxylesterase; Esterase; Auditory neuropathy; Genetics; Toxicology; Enzyme; Hearing loss; Biochemistry; Pesticide; Audiology; Medicine","score_opus":0.008958577636142284,"score_gpt":0.22179343030738718,"score_spread":0.2128348526712449,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2103703726","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.98989165,0.0009491315,0.0042294757,0.00051117886,0.00007120543,0.000060695216,0.0019893746,0.00033290553,0.0019643798],"genre_scores_gemma":[0.9880862,0.0010383626,0.0021410512,0.00021973345,0.000027431564,0.00011574812,0.0009789295,0.00014552138,0.007246915],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99942434,0.00008480134,0.000071799186,0.00018581886,0.0001165656,0.00011667026],"domain_scores_gemma":[0.9987483,0.00016222558,0.0006640904,0.00006727805,0.00006672534,0.0002913701],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00035673234,0.0013433921,0.00045284757,0.0035647675,0.00050558546,0.0007791288,0.0007979878,0.001649988,0.0073857596],"category_scores_gemma":[0.0005061928,0.0008159621,0.00080907374,0.0007072813,0.0012486463,0.00052269665,0.00068620284,0.0024675897,0.00081788143],"study_design_candidate":"bench_or_experimental","study_design_consensus":"bench_or_experimental","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0008993504,0.00020712872,0.0016436613,0.000054532986,0.000054802476,0.0005520568,0.00006907165,0.00022294944,0.99419576,0.00031931343,0.0002120916,0.001569356],"study_design_scores_gemma":[0.00030303118,0.001254479,0.04078645,0.00010988917,0.00034941593,0.0038367473,0.00032893565,0.002895792,0.9462702,0.0008392211,0.0029731386,0.000052628497],"about_ca_topic_score_codex":0.0024120882,"about_ca_topic_score_gemma":0.0034469783,"teacher_disagreement_score":0.0073857596,"about_ca_system_score_codex":0.00085201766,"about_ca_system_score_gemma":0.00046707844,"threshold_uncertainty_score":0.024707854},"labels":[],"label_agreement":null},{"id":"W2103735661","doi":"10.1038/ng.2758","title":"Identification of a rare coding variant in complement 3 associated with age-related macular degeneration","year":2013,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Retinal Diseases and Treatments","field":"Medicine","cited_by":179,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Hospital for Sick Children","funders":"National Eye Institute; National Human Genome Research Institute; National Institute of Mental Health; Medical Research Council; National Institute for Health and Care Research","keywords":"Macular degeneration; Biology; Factor H; Genetics; Complement factor I; Gene; Odds ratio; Complement component 2; Exome; Complement factor B; Case-control study; Complement system; Exome sequencing; Phenotype; Internal medicine; Medicine; Ophthalmology","score_opus":0.011693569443111342,"score_gpt":0.27257918413532606,"score_spread":0.2608856146922147,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2103735661","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.994144,0.00039714397,0.0020391478,0.00083683815,0.00029247307,0.000058447775,0.0004560288,0.00006307747,0.001712811],"genre_scores_gemma":[0.9980287,0.000056436704,0.0009747502,0.00022360886,0.00013457942,0.000008742834,0.00013629404,0.000014798055,0.00042204332],"study_design_codex":"case_report","study_design_gemma":"observational","domain_scores_codex":[0.9991554,0.00014311609,0.0001431715,0.00019082136,0.00022859004,0.0001389337],"domain_scores_gemma":[0.99677,0.0018069544,0.00063617417,0.000124759,0.00023990021,0.00042221954],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00040415733,0.0013613818,0.0007460165,0.002243171,0.0012078085,0.00068672886,0.0012027582,0.004094207,0.0033284368],"category_scores_gemma":[0.005196743,0.00027919284,0.0014282804,0.0010362515,0.0011882993,0.0003600806,0.0007985883,0.0012107793,0.0005456164],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0015819329,0.00026090085,0.04622878,0.00010939629,0.00022202547,0.8422205,0.00068115705,0.0007335661,0.09939426,0.0016775777,0.0009241626,0.0059658187],"study_design_scores_gemma":[0.00044662762,0.0012448165,0.14611053,0.00013157,0.00060975103,0.8088081,0.0006373153,0.0066348123,0.029713335,0.0019965405,0.0034967305,0.00016987401],"about_ca_topic_score_codex":0.0040115123,"about_ca_topic_score_gemma":0.0030151987,"teacher_disagreement_score":0.004094207,"about_ca_system_score_codex":0.0005554802,"about_ca_system_score_gemma":0.0005846926,"threshold_uncertainty_score":0.011134744},"labels":[],"label_agreement":null},{"id":"W2103924961","doi":"10.1038/ng1115","title":"Tailoring the genome: the power of genetic approaches","year":2003,"lang":"en","type":"review","venue":"Nature Genetics","topic":"CRISPR and Genetic Engineering","field":"Biochemistry, Genetics and Molecular Biology","cited_by":78,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Lunenfeld-Tanenbaum Research Institute; University of Toronto; Mount Sinai Hospital","funders":"","keywords":"Biology; Caenorhabditis elegans; Drosophila melanogaster; Genome; Model organism; Inheritance (genetic algorithm); Genetics; Saccharomyces cerevisiae; Drosophila (subgenus); Computational biology; Genetic model; Caenorhabditis; Evolutionary biology; Gene","score_opus":0.022550006843635076,"score_gpt":0.3049980617698931,"score_spread":0.282448054926258,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2103924961","genre_codex":"review","genre_gemma":"review","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"review","genre_consensus":"review","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.00039524538,0.9838907,0.0099769,0.0014636387,0.0010860381,0.000013155435,0.000032545115,0.0001111377,0.0030307292],"genre_scores_gemma":[0.0024804638,0.9876001,0.005949223,0.0012610459,0.0005866017,0.000020861153,0.000058278674,0.000020145048,0.0020233744],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.99928904,0.00009626504,0.00006286606,0.0001213217,0.0003683996,0.00006200413],"domain_scores_gemma":[0.9984981,0.00094003836,0.00010320875,0.000095670315,0.00025774387,0.0001053042],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0019693174,0.0018313254,0.0028551477,0.0019184237,0.00054437696,0.0025358072,0.0028311117,0.0032994982,0.0025877035],"category_scores_gemma":[0.0015710285,0.0005694214,0.00064192154,0.0026780714,0.0031424789,0.0034448074,0.0012626763,0.0050172876,0.0025041574],"study_design_candidate":"not_applicable","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00012781091,0.000091980546,0.00025014093,0.0065931836,0.000083275525,0.00027551292,0.00010732449,0.0020948998,0.024069922,0.0365378,0.03356825,0.8961998],"study_design_scores_gemma":[0.000033786637,0.00008111969,0.00030839388,0.0008707376,0.0000626986,0.0010534489,0.00010226773,0.00051116996,0.008712406,0.02369681,0.96451724,0.0000499987],"about_ca_topic_score_codex":0.0015371068,"about_ca_topic_score_gemma":0.0019023762,"teacher_disagreement_score":0.0032994982,"about_ca_system_score_codex":0.0015444977,"about_ca_system_score_gemma":0.0012964489,"threshold_uncertainty_score":0.01120609},"labels":[],"label_agreement":null},{"id":"W2104599144","doi":"10.1038/ng.641","title":"Germline CBL mutations cause developmental abnormalities and predispose to juvenile myelomonocytic leukemia","year":2010,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Protein Tyrosine Phosphatases","field":"Biochemistry, Genetics and Molecular Biology","cited_by":373,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Canada Research Chairs; University of Toronto","funders":"National Institute of General Medical Sciences; National Cancer Institute; University of California, San Francisco","keywords":"Juvenile myelomonocytic leukemia; Biology; Germline; Neurofibromatosis; Neurofibromin 1; Germline mutation; Costello syndrome; Missense mutation; Noonan syndrome; Genetics; PTPN11; Ubiquitin ligase; Cancer research; Mutation; Internal medicine; Endocrinology; Ubiquitin; KRAS; Haematopoiesis; Stem cell; Medicine","score_opus":0.006363565518400894,"score_gpt":0.2557953281022911,"score_spread":0.24943176258389022,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2104599144","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99620396,0.0003343409,0.00071751163,0.00021933012,0.000030286452,0.000021170712,0.00019325067,0.00010484206,0.0021754329],"genre_scores_gemma":[0.99871147,0.00013516868,0.0004571786,0.000041111634,0.000023991228,0.0000051702455,0.000052566884,0.000022808017,0.0005503775],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.999665,0.000041068906,0.000035769357,0.000058946207,0.000120767996,0.00007845591],"domain_scores_gemma":[0.99904233,0.0003332917,0.0003064217,0.00003795996,0.00003956263,0.00024044618],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00017818395,0.0011453759,0.00041197473,0.002018066,0.0007967,0.0005126211,0.00054335024,0.0011036431,0.0032107397],"category_scores_gemma":[0.00097157515,0.0003997897,0.0002970845,0.0008380744,0.0011061629,0.00023300762,0.00077208003,0.00087585073,0.000389016],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0011969799,0.00015285089,0.061503615,0.00013809059,0.00009104819,0.41119945,0.00067605573,0.0008287225,0.51047945,0.002073629,0.0010373817,0.010622717],"study_design_scores_gemma":[0.0002693424,0.00035329195,0.2933759,0.00006398102,0.00026799468,0.59106004,0.0008680378,0.002506821,0.1029199,0.0015208597,0.006679987,0.00011389621],"about_ca_topic_score_codex":0.0030776542,"about_ca_topic_score_gemma":0.004296321,"teacher_disagreement_score":0.0032107397,"about_ca_system_score_codex":0.0006256522,"about_ca_system_score_gemma":0.00044650966,"threshold_uncertainty_score":0.010741055},"labels":[],"label_agreement":null},{"id":"W2105096699","doi":"10.1038/ng.3336","title":"Genome-wide significant risk associations for mucinous ovarian carcinoma","year":2015,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Ovarian cancer diagnosis and treatment","field":"Medicine","cited_by":84,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Women's College Hospital; Simon Fraser University; BC Cancer Agency; University of Toronto; Canada's Michael Smith Genome Sciences Centre; Public Health Ontario; University of British Columbia","funders":"Eunice Kennedy Shriver National Institute of Child Health and Human Development; National Center for Advancing Translational Sciences; National Institute of Allergy and Infectious Diseases; European Commission; Wellcome Trust; Francis Crick Institute; National Cancer Institute; Cancer Research UK; Roswell Park Cancer Institute; Ovarian Cancer Research Fund","keywords":"Biology; Genome-wide association study; Ovarian cancer; Single-nucleotide polymorphism; Expression quantitative trait loci; Ovarian carcinoma; Genetic association; Colorectal cancer; Genetics; Cancer research; Gene; Cancer; Genotype","score_opus":0.025563677635819394,"score_gpt":0.2864805752735155,"score_spread":0.2609168976376961,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2105096699","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.98947984,0.0048869736,0.00076412584,0.001418561,0.00013754424,0.000007397849,0.0014109373,0.000050134826,0.0018444988],"genre_scores_gemma":[0.9980665,0.00053897896,0.00029182254,0.00010888494,0.00009785743,0.0000035497037,0.00036138398,0.000013269012,0.0005178426],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9994417,0.00018878636,0.00005027559,0.00014318673,0.00007291972,0.000103117796],"domain_scores_gemma":[0.9979382,0.0008462015,0.0005814782,0.00022625612,0.000112486065,0.00029528336],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0007241781,0.00044691822,0.0003772529,0.0008571041,0.00048002123,0.00080650044,0.00054194004,0.000972517,0.0047962116],"category_scores_gemma":[0.003316285,0.0003391482,0.0015792842,0.0012034499,0.00038616537,0.0003648853,0.0006518187,0.0012135544,0.00030297457],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0016774723,0.000079149926,0.9699985,0.00014801446,0.0028854457,0.0011277375,0.00016567335,0.0005256,0.011716811,0.0005568312,0.001530496,0.009588218],"study_design_scores_gemma":[0.000066394634,0.00008609747,0.99461836,0.00002310644,0.0012923701,0.0008247794,0.00012065909,0.0006205785,0.0006109954,0.00059812184,0.0011267308,0.0000118202215],"about_ca_topic_score_codex":0.004149541,"about_ca_topic_score_gemma":0.0061683105,"teacher_disagreement_score":0.0047962116,"about_ca_system_score_codex":0.00020126997,"about_ca_system_score_gemma":0.00038207293,"threshold_uncertainty_score":0.016044915},"labels":[],"label_agreement":null},{"id":"W2105369704","doi":"10.1038/ng.2564","title":"GWAS meta-analysis and replication identifies three new susceptibility loci for ovarian cancer","year":2013,"lang":"en","type":"article","venue":"Nature Genetics","topic":"RNA modifications and cancer","field":"Biochemistry, Genetics and Molecular Biology","cited_by":361,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Lunenfeld-Tanenbaum Research Institute; Mount Sinai Hospital; University of Toronto; BC Cancer Agency; Public Health Ontario; McGill University and Génome Québec Innovation Centre; McGill University Health Centre; Women's College Hospital; Alberta Health Services; University of Calgary; McGill University","funders":"David Geffen School of Medicine, University of California, Los Angeles; National Cancer Institute; University Hospital Southampton NHS Foundation Trust; Audrey and Theodor Geisel School of Medicine at Dartmouth; Haukeland Universitetssjukehus; Department of Obstetrics, Gynecology and Reproductive Sciences, University of Pittsburgh; Dartmouth College; Deutsches Krebsforschungszentrum; Pomorski Uniwersytet Medyczny W Szczecinie; Rigshospitalet; Universitetet i Bergen; Peter MacCallum Cancer Centre; University of Southampton; Wellcome Trust; University of Southern California; Cancer Research UK; Herlev Hospital; European Commission; Magee-Womens Research Institute; Medizinischen Hochschule Hannover; Monash University; Brigham and Women's Hospital; Universitätsklinikum Jena; University of Pittsburgh; Ovarian Cancer Research Fund","keywords":"Biology; Genome-wide association study; Ovarian cancer; Replication (statistics); Genetics; Computational biology; Meta-analysis; Cancer; Single-nucleotide polymorphism; Internal medicine; Virology; Gene; Genotype","score_opus":0.03417747130833292,"score_gpt":0.322337091631445,"score_spread":0.2881596203231121,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2105369704","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.95521367,0.01686331,0.018860627,0.0016722196,0.00054513564,0.00008771519,0.0038087463,0.00044873846,0.002499814],"genre_scores_gemma":[0.99478513,0.0008651294,0.0025695446,0.00026863726,0.00012359419,0.00003790614,0.000769302,0.00008835507,0.00049248314],"study_design_codex":"observational","study_design_gemma":"meta_analysis","domain_scores_codex":[0.9948696,0.0018285975,0.00045938438,0.001774653,0.00062907126,0.00043877403],"domain_scores_gemma":[0.98729986,0.005960096,0.0015075305,0.0038746006,0.0007557847,0.00060201326],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.007111749,0.0014276182,0.0017281126,0.0019649644,0.001211881,0.0021623764,0.0013215785,0.0016710875,0.003362684],"category_scores_gemma":[0.01541255,0.0010913563,0.0061404663,0.003088169,0.0008334237,0.0007440421,0.001331958,0.0019308268,0.0003815286],"study_design_candidate":"meta_analysis","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.006964565,0.00010664506,0.8738551,0.00067922485,0.063270085,0.0019334935,0.00068224134,0.0010316584,0.029877976,0.001523698,0.0022762718,0.017799133],"study_design_scores_gemma":[0.0013950475,0.0008194935,0.89614844,0.00013183297,0.075344816,0.0027674832,0.00046445828,0.0033832332,0.0069595366,0.0058727954,0.006604951,0.00010792399],"about_ca_topic_score_codex":0.0047170212,"about_ca_topic_score_gemma":0.007208423,"teacher_disagreement_score":0.007111749,"about_ca_system_score_codex":0.0004962412,"about_ca_system_score_gemma":0.0010264271,"threshold_uncertainty_score":0.037610948},"labels":[],"label_agreement":null},{"id":"W2106650442","doi":"10.1038/ng.909","title":"A copy number variation morbidity map of developmental delay","year":2011,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Genomic variations and chromosomal abnormalities","field":"Biochemistry, Genetics and Molecular Biology","cited_by":1404,"is_retracted":false,"has_abstract":false,"route_ca_aff":false,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"","funders":"National Heart, Lung, and Blood Institute; Canadian Institutes of Health Research; National Institutes of Health; Wellcome Trust; Eunice Kennedy Shriver National Institute of Child Health and Human Development; Howard Hughes Medical Institute","keywords":"Copy-number variation; Intellectual disability; Autism; Biology; Exome sequencing; Candidate gene; Genetics; Epilepsy; Craniofacial; Comparative genomic hybridization; Autism spectrum disorder; Developmental disorder; Exome; Phenotype; Genome; Gene; Medicine; Neuroscience; Psychiatry","score_opus":0.011686657375122679,"score_gpt":0.23086213504483816,"score_spread":0.21917547766971548,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2106650442","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.98954797,0.00071410567,0.0046875444,0.00034884206,0.000034968692,0.000022622227,0.0013223706,0.00012157828,0.00320014],"genre_scores_gemma":[0.99571276,0.00031601518,0.0013422162,0.000056151628,0.000026887994,0.000012934572,0.0006880724,0.000031518404,0.0018133126],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9997646,0.00002007328,0.000014673927,0.000086666754,0.00007589851,0.000038089373],"domain_scores_gemma":[0.99947256,0.00023906273,0.00010750296,0.00005126564,0.000048726793,0.00008088364],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00013038519,0.0004091556,0.0003674168,0.0015516912,0.00029871732,0.00040629317,0.00057100377,0.0003744358,0.0064429725],"category_scores_gemma":[0.00064516574,0.00026228483,0.00048756984,0.0007131358,0.00026972,0.00021982339,0.00041166306,0.00063738745,0.0005148003],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0010223383,0.000107748216,0.037959415,0.00008789558,0.00017667732,0.0046664034,0.00017963903,0.0014482007,0.9276581,0.0024051806,0.00066266983,0.023625687],"study_design_scores_gemma":[0.000121369536,0.00073102,0.70915467,0.000035584468,0.00044858514,0.023449523,0.00021104133,0.0067074304,0.24661425,0.005243054,0.0072181914,0.00006540449],"about_ca_topic_score_codex":0.0026927383,"about_ca_topic_score_gemma":0.0014039048,"teacher_disagreement_score":0.0064429725,"about_ca_system_score_codex":0.00034059945,"about_ca_system_score_gemma":0.00022784749,"threshold_uncertainty_score":0.021553874},"labels":[],"label_agreement":null},{"id":"W2106779017","doi":"10.1038/ng.717","title":"Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci","year":2010,"lang":"en","type":"review","venue":"Nature Genetics","topic":"Inflammatory Bowel Disease","field":"Biochemistry, Genetics and Molecular Biology","cited_by":2581,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Université de Montréal; Montreal Heart Institute; Hospital for Sick Children; University of Toronto; SickKids Foundation; Mount Sinai Hospital; Jewish General Hospital","funders":"National Institute of Diabetes and Digestive and Kidney Diseases; National Heart, Lung, and Blood Institute; National Health and Medical Research Council; National Institute of Arthritis and Musculoskeletal and Skin Diseases; Medical Research Council; National Institutes of Health; Exzellenzclusters Entzündungsforschung; Fonds De La Recherche Scientifique - FNRS; Cedars-Sinai Medical Center; Deutsche Forschungsgemeinschaft; King's College London; National Institute for Health and Care Research; Action Medical Research; National Center for Research Resources; Fonds Wetenschappelijk Onderzoek; Crohn's and Colitis Foundation; Wellcome Trust; Abbott Laboratories; Crohn's and Colitis Foundation of America","keywords":"Biology; Genome-wide association study; Genetics; Genome; In silico; Genetic association; Disease; Gene; Crohn's disease; Single-nucleotide polymorphism; Genotype","score_opus":0.022818850057355088,"score_gpt":0.3255244616539011,"score_spread":0.302705611596546,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2106779017","genre_codex":"review","genre_gemma":"review","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"review","genre_consensus":"review","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.0012730664,0.9960855,0.0007151837,0.00095660903,0.00026607528,0.00000562059,0.00022735978,0.000021107235,0.00044949073],"genre_scores_gemma":[0.02570191,0.96788365,0.001951932,0.0020632844,0.001132128,0.000027755248,0.00078003074,0.000025425015,0.00043381125],"study_design_codex":"design_other","study_design_gemma":"meta_analysis","domain_scores_codex":[0.9983523,0.00066845625,0.00018480034,0.00040475893,0.00032793477,0.00006175324],"domain_scores_gemma":[0.9927846,0.0058749253,0.00046297244,0.00025489484,0.00050598214,0.000116616364],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0050816857,0.0017339397,0.0057650553,0.0015728754,0.00016507646,0.0013763268,0.0013239981,0.0016292522,0.003032387],"category_scores_gemma":[0.0083412435,0.00053603516,0.004140066,0.0025200034,0.00038935005,0.0006787216,0.000864635,0.0014391012,0.00053804973],"study_design_candidate":"meta_analysis","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0023127554,0.00006158678,0.024138413,0.049141016,0.06329796,0.0013485199,0.00009687944,0.001455324,0.002721369,0.0016716933,0.036145285,0.8176092],"study_design_scores_gemma":[0.0028060814,0.0011286744,0.16928713,0.02846534,0.33118728,0.010222323,0.00025697745,0.001718452,0.0036434676,0.012652901,0.43827742,0.0003538971],"about_ca_topic_score_codex":0.001641851,"about_ca_topic_score_gemma":0.0047433106,"teacher_disagreement_score":0.0057650553,"about_ca_system_score_codex":0.0005964658,"about_ca_system_score_gemma":0.0012304614,"threshold_uncertainty_score":0.02687484},"labels":[],"label_agreement":null},{"id":"W2107139378","doi":"10.1038/ng.3405","title":"Trans-ancestry genome-wide association study identifies 12 genetic loci influencing blood pressure and implicates a role for DNA methylation","year":2015,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Genetic Associations and Epidemiology","field":"Biochemistry, Genetics and Molecular Biology","cited_by":376,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Ottawa","funders":"National Center for Research Resources; U.S. National Library of Medicine; National Institute of Environmental Health Sciences; National Center for Advancing Translational Sciences; Wellcome Trust; Nederlandse Organisatie voor Wetenschappelijk Onderzoek; National Human Genome Research Institute; Fogarty International Center; National Institute of Mental Health; National Heart, Lung, and Blood Institute; National Institute on Aging; National Institute of Diabetes and Digestive and Kidney Diseases; Biotechnology and Biological Sciences Research Council; Medical Research Council; Agency for Healthcare Research and Quality; National Institute for Health and Care Research; National Cancer Institute; British Heart Foundation","keywords":"Biology; DNA methylation; Genetics; Genome-wide association study; Methylation; Genetic association; Genome; Genetic genealogy; DNA; Computational biology; Single-nucleotide polymorphism; Gene; Genotype; Population; Gene expression","score_opus":0.014224498587856254,"score_gpt":0.28191880367447925,"score_spread":0.267694305086623,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2107139378","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99452055,0.000725431,0.0029577748,0.00018574932,0.000036909547,0.000010216542,0.000587581,0.000045354594,0.0009305614],"genre_scores_gemma":[0.99760664,0.0002230635,0.0012602343,0.000044395438,0.000020258598,0.000006891491,0.00031774092,0.000016545879,0.00050426926],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9991146,0.00032008026,0.00006485447,0.00029016647,0.00011989967,0.0000903018],"domain_scores_gemma":[0.99880886,0.0002886273,0.00031294455,0.00019434393,0.00016497185,0.00023023559],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0008723243,0.00062416145,0.00056756526,0.0011820552,0.00084299,0.0006395153,0.00054610724,0.00067623623,0.0026662266],"category_scores_gemma":[0.0017429905,0.0003353794,0.00088598847,0.0018623653,0.0003931554,0.0002458329,0.000909292,0.0010527587,0.00027104578],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0019225703,0.00010969644,0.9384402,0.000058869286,0.0018069,0.0007606328,0.00048638476,0.00016078743,0.045005858,0.0005255624,0.0003897061,0.010332828],"study_design_scores_gemma":[0.000047892518,0.00023632949,0.99206007,0.000013369646,0.0008666134,0.0016380177,0.00019040167,0.00087942695,0.0028965708,0.0003750202,0.00078121945,0.000015141358],"about_ca_topic_score_codex":0.0070129978,"about_ca_topic_score_gemma":0.009962849,"teacher_disagreement_score":0.0070129978,"about_ca_system_score_codex":0.00016691629,"about_ca_system_score_gemma":0.000305108,"threshold_uncertainty_score":0.013944328},"labels":[],"label_agreement":null},{"id":"W2107766358","doi":"10.1038/ng.501","title":"Genome-wide association study identifies five loci associated with lung function","year":2009,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Epigenetics and DNA Methylation","field":"Biochemistry, Genetics and Molecular Biology","cited_by":598,"is_retracted":false,"has_abstract":false,"route_ca_aff":false,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"","funders":"National Institute of Allergy and Infectious Diseases; National Institute of Child Health and Human Development; National Institute of Diabetes and Digestive and Kidney Diseases; Biocenter, University of Oulu; National Heart, Lung, and Blood Institute; NIHR Cambridge Biomedical Research Centre; Helmholtz Zentrum München; Wellcome Trust; Cancer Research UK; Asthma and Lung UK; Biotechnology and Biological Sciences Research Council; Medical Research Council; Directorate for Biological Sciences; National Institutes of Health; Oulun Yliopisto; European Commission; University of Bristol; Vetenskapsrådet; Healthway; British Lung Foundation; National Institute of Mental Health; International Osteoporosis Foundation; Bundesministerium für Bildung und Forschung; National Institute for Health and Care Research; Genome Canada; British Heart Foundation; Scottish Government; AstraZeneca; Tays; King's College London; Juvenile Diabetes Research Foundation International","keywords":"Genome-wide association study; Biology; Genotyping; COPD; Vital capacity; Locus (genetics); Genetics; Pulmonary function testing; Genetic association; In silico; Lung function; Internal medicine; Bioinformatics; Single-nucleotide polymorphism; Genotype; Medicine; Lung; Gene; Diffusing capacity","score_opus":0.004644334868257112,"score_gpt":0.24222982755557076,"score_spread":0.23758549268731366,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2107766358","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99756783,0.0006861428,0.00085156946,0.00011938524,0.000013387488,0.000006516376,0.000268286,0.00002488303,0.0004619274],"genre_scores_gemma":[0.9988237,0.0001241028,0.00048685155,0.00003598715,0.0000115759685,0.000005332825,0.00017673319,0.0000069912658,0.000328753],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99948126,0.00014397647,0.00004538581,0.00017895942,0.00008000875,0.00007037017],"domain_scores_gemma":[0.99862695,0.0006026486,0.00032062805,0.00010278612,0.00009069217,0.0002563281],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00082539866,0.00048393942,0.00052227656,0.0016069479,0.00062656106,0.00053401926,0.00061048556,0.0007894972,0.002017028],"category_scores_gemma":[0.0011369009,0.00033650387,0.0006714115,0.0015538083,0.0005701154,0.00018392483,0.00050760515,0.00082911504,0.00023340875],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0040023224,0.00035555864,0.86744726,0.00009877397,0.0015901196,0.0015660396,0.0003070022,0.0002880797,0.11390831,0.00044236405,0.0004925324,0.009501673],"study_design_scores_gemma":[0.00008586249,0.00019686292,0.9939587,0.0000064832157,0.00046357256,0.0010221343,0.00008847771,0.0004583392,0.0031390877,0.0001960928,0.00037285447,0.000011407332],"about_ca_topic_score_codex":0.0027858168,"about_ca_topic_score_gemma":0.0036057679,"teacher_disagreement_score":0.0027858168,"about_ca_system_score_codex":0.00021072688,"about_ca_system_score_gemma":0.0002951425,"threshold_uncertainty_score":0.0067476034},"labels":[],"label_agreement":null},{"id":"W2108305936","doi":"10.1038/ng.2652","title":"Genome-wide association study identifies multiple risk loci for chronic lymphocytic leukemia","year":2013,"lang":"en","type":"review","venue":"Nature Genetics","topic":"Chronic Lymphocytic Leukemia Research","field":"Medicine","cited_by":211,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Simon Fraser University; BC Cancer Agency","funders":"National Institute of Environmental Health Sciences; National Cancer Institute; National Human Genome Research Institute; National Institutes of Health","keywords":"Chronic lymphocytic leukemia; Genome-wide association study; Biology; Single-nucleotide polymorphism; Locus (genetics); Genetics; Genetic association; Leukemia; Gene; Genotype","score_opus":0.030421998552550258,"score_gpt":0.35079895933046834,"score_spread":0.3203769607779181,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2108305936","genre_codex":"review","genre_gemma":"review","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"review","genre_consensus":"review","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.000094845054,0.9983188,0.00015447079,0.00075403665,0.00023947595,0.0000028999398,0.000033872366,0.0000075002245,0.00039419063],"genre_scores_gemma":[0.00074441405,0.99767786,0.0002353132,0.00056993286,0.0004615558,0.0000055157057,0.000058393936,0.000001515856,0.00024551005],"study_design_codex":"design_other","study_design_gemma":"observational","domain_scores_codex":[0.9996069,0.000075365315,0.000064512686,0.00009083694,0.00013299908,0.000029467355],"domain_scores_gemma":[0.99862397,0.0007854159,0.00016223383,0.000036106205,0.00028939763,0.000102885744],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0015136942,0.0009974916,0.0018905308,0.0020155562,0.00024689274,0.0008695559,0.0013143001,0.0014238546,0.0020285328],"category_scores_gemma":[0.0020404293,0.00033324858,0.0006559669,0.0024965033,0.00067485264,0.0008525915,0.0008571429,0.0019295684,0.001022791],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00018416421,0.00004624546,0.001519081,0.008485214,0.00032229236,0.00026721548,0.000027668093,0.00020490818,0.00086517073,0.0018525238,0.04552591,0.94069964],"study_design_scores_gemma":[0.00012707399,0.00011586827,0.0083213365,0.006587598,0.0010951994,0.0017186251,0.00010460829,0.00015199615,0.0004809683,0.005067315,0.97616583,0.000063524],"about_ca_topic_score_codex":0.002042791,"about_ca_topic_score_gemma":0.0043635587,"teacher_disagreement_score":0.002042791,"about_ca_system_score_codex":0.00071980833,"about_ca_system_score_gemma":0.0015720498,"threshold_uncertainty_score":0.008005261},"labels":[],"label_agreement":null},{"id":"W2108479075","doi":"10.1038/ng1921","title":"Genome assembly comparison identifies structural variants in the human genome","year":2006,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Genomic variations and chromosomal abnormalities","field":"Biochemistry, Genetics and Molecular Biology","cited_by":165,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"SickKids Foundation; Hospital for Sick Children; University of Toronto","funders":"Wellcome Trust","keywords":"Biology; Structural variation; Genetics; Genome; Copy-number variation; Human genome; Single-nucleotide polymorphism; Computational biology; Reference genome; DNA sequencing; Whole genome sequencing; SNP array; Sequence assembly; Sequence (biology); Segmental duplication; Genome project; DNA; Gene; Genotype","score_opus":0.008035278375324502,"score_gpt":0.25727572933149995,"score_spread":0.24924045095617545,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2108479075","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9836089,0.0012179137,0.008221076,0.0002916405,0.000061602346,0.00002400435,0.0044992794,0.0004320785,0.0016436044],"genre_scores_gemma":[0.96683395,0.0004136288,0.013889782,0.000151205,0.000035602035,0.000023355376,0.017039334,0.0002280679,0.001385115],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.99959296,0.00010149922,0.000040824238,0.00012330816,0.00009194586,0.000049392856],"domain_scores_gemma":[0.9992003,0.00036877953,0.000096671014,0.00013124346,0.00010763112,0.00009535898],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0005116969,0.00040786288,0.00043886728,0.0019385722,0.0007067373,0.0006746983,0.00037145166,0.0005585236,0.0035627189],"category_scores_gemma":[0.0016068117,0.00025648528,0.00070251775,0.0013732964,0.00027508024,0.00026477527,0.00040915614,0.0006825403,0.00065520906],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0071388395,0.00037161016,0.06990014,0.000548106,0.0009869167,0.0024529689,0.0006687363,0.0047945017,0.840039,0.0026514393,0.0061061755,0.064341575],"study_design_scores_gemma":[0.00026795856,0.00095102034,0.71549493,0.000083119405,0.0013871471,0.007141093,0.00042367633,0.025719577,0.21627751,0.0033230947,0.028828647,0.00010222165],"about_ca_topic_score_codex":0.0023584443,"about_ca_topic_score_gemma":0.0047928602,"teacher_disagreement_score":0.0035627189,"about_ca_system_score_codex":0.00036061098,"about_ca_system_score_gemma":0.00045833408,"threshold_uncertainty_score":0.011918485},"labels":[],"label_agreement":null},{"id":"W2109378245","doi":"10.1038/ng.2854","title":"Application of a 5-tiered scheme for standardized classification of 2,360 unique mismatch repair gene variants in the InSiGHT locus-specific database","year":2013,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Genetic factors in colorectal cancer","field":"Medicine","cited_by":476,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Memorial University of Newfoundland; University of Toronto","funders":"National Cancer Institute; Medical Research Council; Cancer Research UK; Wellcome Trust","keywords":"Biology; Locus (genetics); Genetics; Computational biology; Gene; Database; Computer science","score_opus":0.022757409981581593,"score_gpt":0.2974771378066685,"score_spread":0.2747197278250869,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2109378245","genre_codex":"methods","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":null,"domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.09551089,0.0005735645,0.7961751,0.0009983057,0.00030196132,0.0034048166,0.06759088,0.02872631,0.0067181364],"genre_scores_gemma":[0.14835387,0.00018958935,0.7807827,0.00021835027,0.00005781873,0.0012968399,0.06642643,0.000853815,0.0018206333],"study_design_codex":"design_other","study_design_gemma":"observational","domain_scores_codex":[0.9885206,0.0024910637,0.004249214,0.0020939803,0.0020281004,0.0006168962],"domain_scores_gemma":[0.9680911,0.006880405,0.0021835864,0.012233778,0.009528685,0.0010824468],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.014495091,0.00078085694,0.001508917,0.011585234,0.0013933198,0.0042054434,0.0014401219,0.0010519035,0.008639562],"category_scores_gemma":[0.04527231,0.0006504057,0.0014493025,0.008197539,0.0005978728,0.0037032817,0.004450587,0.0015150879,0.0039006784],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0035481136,0.0007874977,0.11125811,0.001163055,0.00069086,0.0005576249,0.0010673658,0.008533122,0.035758715,0.019658351,0.048346195,0.768631],"study_design_scores_gemma":[0.0016579467,0.0023850582,0.19836466,0.0013859072,0.0019617365,0.0042131892,0.0020624173,0.39423788,0.1016559,0.068761945,0.22226886,0.0010444828],"about_ca_topic_score_codex":0.0076021776,"about_ca_topic_score_gemma":0.01015143,"teacher_disagreement_score":0.014495091,"about_ca_system_score_codex":0.0014361003,"about_ca_system_score_gemma":0.0048562493,"threshold_uncertainty_score":0.07665825},"labels":[],"label_agreement":null},{"id":"W2109625917","doi":"10.1038/ng.3014","title":"Genetic association study of QT interval highlights role for calcium signaling pathways in myocardial repolarization","year":2014,"lang":"en","type":"review","venue":"Nature Genetics","topic":"Cardiac electrophysiology and arrhythmias","field":"Medicine","cited_by":335,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"SickKids Foundation; Hospital for Sick Children; Ontario Institute for Cancer Research","funders":"National Center for Advancing Translational Sciences; British Heart Foundation; National Institute of Diabetes and Digestive and Kidney Diseases; National Heart, Lung, and Blood Institute; National Human Genome Research Institute; Economic and Social Research Council; National Institute of General Medical Sciences; Medical Research Council; National Institute for Health and Care Research","keywords":"Biology; Repolarization; QT interval; Association (psychology); Signal transduction; Genetic association; Calcium; Internal medicine; Genetics; Single-nucleotide polymorphism; Neuroscience; Genotype; Medicine; Gene; Electrophysiology","score_opus":0.017770262870448684,"score_gpt":0.3075967819283621,"score_spread":0.2898265190579134,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2109625917","genre_codex":"review","genre_gemma":"review","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"review","genre_consensus":"review","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.0007736617,0.996194,0.0007762306,0.00074074266,0.00025334157,0.0000054132706,0.000056942717,0.000014130353,0.0011854075],"genre_scores_gemma":[0.005746481,0.99065053,0.0011341426,0.00068048557,0.0007521241,0.000010231204,0.00013152628,0.000004532356,0.00088988343],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.99980897,0.000032905613,0.00003707469,0.000053264783,0.000053311946,0.000014532315],"domain_scores_gemma":[0.99954236,0.00027229724,0.00007654304,0.000011030499,0.0000691272,0.000028687384],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0004151519,0.0007830126,0.001179233,0.0014444957,0.00013389833,0.00052484416,0.0007324011,0.00085229985,0.0021005184],"category_scores_gemma":[0.0009200283,0.00015657827,0.00048889057,0.0014395568,0.00034009505,0.00061228964,0.00053362444,0.000990023,0.0007045285],"study_design_candidate":"not_applicable","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00017252263,0.00006007851,0.0027907654,0.007071071,0.00039427096,0.0019249725,0.000050591952,0.00041482487,0.0052697766,0.0024705671,0.016691716,0.96268886],"study_design_scores_gemma":[0.00016384211,0.0002558866,0.016437532,0.006310682,0.0019998238,0.018255558,0.00017241934,0.00048153943,0.0026024936,0.008814178,0.9444091,0.000096925134],"about_ca_topic_score_codex":0.00086570426,"about_ca_topic_score_gemma":0.0012485464,"teacher_disagreement_score":0.0021005184,"about_ca_system_score_codex":0.00024884383,"about_ca_system_score_gemma":0.0006263338,"threshold_uncertainty_score":0.0070269704},"labels":[],"label_agreement":null},{"id":"W2109899118","doi":"10.1038/ng.549","title":"Genome-wide association identifies multiple ulcerative colitis susceptibility loci","year":2010,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Inflammatory Bowel Disease","field":"Biochemistry, Genetics and Molecular Biology","cited_by":680,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Toronto; Mount Sinai Hospital; Centre Hospitalier Universitaire Sainte-Justine; Centre Hospitalier de l’Université de Montréal; Université de Montréal; Montreal Heart Institute","funders":"National Center for Research Resources; National Institute of Allergy and Infectious Diseases; National Institute of Diabetes and Digestive and Kidney Diseases; National Cancer Institute; National Heart, Lung, and Blood Institute","keywords":"Ulcerative colitis; Genome-wide association study; Inflammatory bowel disease; Single-nucleotide polymorphism; Biology; Colitis; Pathogenesis; Disease; Genetic predisposition; Genetic association; Genetics; Immunology; Medicine; Internal medicine; Genotype; Gene","score_opus":0.00416546060674571,"score_gpt":0.23679715313674082,"score_spread":0.2326316925299951,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2109899118","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99551314,0.0014255284,0.0012215392,0.00039681635,0.000043354663,0.0000070718,0.000355477,0.00004545623,0.0009916705],"genre_scores_gemma":[0.99781215,0.00037255243,0.001034417,0.00008159016,0.000042573753,0.000005960932,0.00023746186,0.000013284368,0.00039991253],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9993311,0.00019764631,0.000049964518,0.00018588608,0.00014865781,0.00008682752],"domain_scores_gemma":[0.99891865,0.00042540702,0.0003121592,0.000089048204,0.00007030857,0.00018449704],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0007745723,0.0004947442,0.0005031214,0.0016977579,0.00047976186,0.00078559364,0.00049671775,0.0008634067,0.0020908793],"category_scores_gemma":[0.0010748366,0.00037664885,0.0006542466,0.0014856028,0.00048338718,0.00018557844,0.0004943275,0.0007863569,0.00026540257],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.006485958,0.00034785512,0.6673376,0.00019190299,0.0022117756,0.0037292761,0.0003072961,0.0007905278,0.2910858,0.0011950493,0.0015031621,0.024813697],"study_design_scores_gemma":[0.0001406843,0.00017935339,0.9883767,0.000016297929,0.0007340901,0.0022687698,0.00010724306,0.0008013186,0.005539634,0.00066078315,0.0011538158,0.000021220249],"about_ca_topic_score_codex":0.0017098971,"about_ca_topic_score_gemma":0.0033286912,"teacher_disagreement_score":0.0020908793,"about_ca_system_score_codex":0.00021120442,"about_ca_system_score_gemma":0.0002622363,"threshold_uncertainty_score":0.0069946647},"labels":[],"label_agreement":null},{"id":"W2110283302","doi":"10.1038/ng1786","title":"The centrosomal protein nephrocystin-6 is mutated in Joubert syndrome and activates transcription factor ATF4","year":2006,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Genetic and Kidney Cyst Diseases","field":"Biochemistry, Genetics and Molecular Biology","cited_by":572,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Simon Fraser University","funders":"National Institute of Diabetes and Digestive and Kidney Diseases; National Eye Institute","keywords":"Biology; Nephronophthisis; Joubert syndrome; Cilium; Ciliopathies; Centrosome; Transcription factor; Retinal degeneration; Cell biology; Zebrafish; Genetics; Phenotype; Gene; Cell cycle","score_opus":0.0031978671452284222,"score_gpt":0.21012521425957725,"score_spread":0.20692734711434882,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2110283302","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99680126,0.0006271293,0.0013946444,0.00016140749,0.000052974247,0.000005946562,0.00015237441,0.00006441296,0.0007398076],"genre_scores_gemma":[0.9977471,0.00018630663,0.001094022,0.000038365015,0.000013748837,0.000005383203,0.00015297785,0.000019846946,0.0007422284],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9997609,0.000041160052,0.000030740055,0.000038064503,0.00009284235,0.00003630111],"domain_scores_gemma":[0.99968266,0.00005752537,0.000120170174,0.000019480605,0.00003081658,0.00008940506],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00017818344,0.00050852745,0.0003076369,0.00066632626,0.0003725187,0.0002612847,0.0004191861,0.00071869756,0.0012166313],"category_scores_gemma":[0.00054491474,0.00028610296,0.00033888314,0.00021573127,0.0004698524,0.00026352963,0.0004594281,0.00046194988,0.000325003],"study_design_candidate":"bench_or_experimental","study_design_consensus":"bench_or_experimental","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00038221377,0.000021704558,0.00678101,0.000057942,0.00003880904,0.009933746,0.000085247564,0.0003362054,0.9790055,0.00061981764,0.0002871612,0.0024505018],"study_design_scores_gemma":[0.000099189885,0.00017804003,0.08484788,0.00003423037,0.00010524747,0.058883157,0.00027314512,0.0039543365,0.8444657,0.0011962376,0.0059303227,0.00003257543],"about_ca_topic_score_codex":0.0007724278,"about_ca_topic_score_gemma":0.0010209257,"teacher_disagreement_score":0.0012166313,"about_ca_system_score_codex":0.00037347418,"about_ca_system_score_gemma":0.00026253576,"threshold_uncertainty_score":0.004069984},"labels":[],"label_agreement":null},{"id":"W2110535520","doi":"10.1038/ng.760","title":"Common variants in ZNF365 are associated with both mammographic density and breast cancer risk","year":2011,"lang":"en","type":"review","venue":"Nature Genetics","topic":"Global Cancer Incidence and Screening","field":"Medicine","cited_by":124,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Ontario Institute for Cancer Research; Lunenfeld-Tanenbaum Research Institute; Mount Sinai Hospital; University of Toronto; Public Health Ontario; Hospital for Sick Children","funders":"National Cancer Institute; Cancer Research UK","keywords":"Breast cancer; MAMMOGRAPHIC DENSITY; Genome-wide association study; Biology; Body mass index; Risk factors for breast cancer; Genetic association; Oncology; Locus (genetics); Mammography; Meta-analysis; Cancer; Genetics; Internal medicine; Single-nucleotide polymorphism; Medicine; Genotype; Gene; Endocrinology","score_opus":0.04487574341405276,"score_gpt":0.3319100064140385,"score_spread":0.28703426299998575,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2110535520","genre_codex":"review","genre_gemma":"review","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"review","genre_consensus":"review","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.0022052198,0.99548656,0.0003816715,0.0006933753,0.00021624845,0.000005613322,0.00012665805,0.000017646713,0.0008669899],"genre_scores_gemma":[0.017640045,0.978829,0.0009765887,0.0005631299,0.00045809153,0.000015126797,0.00034664854,0.0000045547145,0.001166755],"study_design_codex":"design_other","study_design_gemma":"observational","domain_scores_codex":[0.99978393,0.000032523607,0.00004170641,0.000052645424,0.00007199229,0.000017209522],"domain_scores_gemma":[0.99965775,0.00016404229,0.00010384826,0.0000076102347,0.000049115297,0.000017758448],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00034764627,0.0007467812,0.0013975558,0.0012488252,0.000119328935,0.00036948817,0.00071623037,0.00070633256,0.0017022468],"category_scores_gemma":[0.0010356747,0.000210141,0.0005734559,0.0018698287,0.0002381506,0.00029292426,0.00037617894,0.00052703463,0.00037935094],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00038250923,0.000042805616,0.0114365965,0.009503918,0.0013163028,0.0011587724,0.000045828605,0.00048019105,0.002269463,0.0012053463,0.019315213,0.9528431],"study_design_scores_gemma":[0.0003779638,0.00029627615,0.08475168,0.007871497,0.007652001,0.020717205,0.00020026533,0.0008126231,0.0027377477,0.0060447194,0.868443,0.0000950848],"about_ca_topic_score_codex":0.0033379523,"about_ca_topic_score_gemma":0.0055164397,"teacher_disagreement_score":0.0033379523,"about_ca_system_score_codex":0.00041507,"about_ca_system_score_gemma":0.00065825,"threshold_uncertainty_score":0.006637037},"labels":[],"label_agreement":null},{"id":"W2110747516","doi":"10.1038/ng.653","title":"Identity-by-descent filtering of exome sequence data identifies PIGV mutations in hyperphosphatasia mental retardation syndrome","year":2010,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Genomics and Rare Diseases","field":"Biochemistry, Genetics and Molecular Biology","cited_by":300,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Toronto","funders":"Canadian Institutes of Health Research","keywords":"Exome sequencing; Biology; Exome; Genetics; Mutation; Gene","score_opus":0.014773867251859167,"score_gpt":0.290576730491805,"score_spread":0.27580286323994585,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2110747516","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.996241,0.00019970062,0.0021797994,0.00004355235,0.000011801674,0.000013636067,0.0007800542,0.00007061778,0.0004598433],"genre_scores_gemma":[0.9920054,0.00010923396,0.004381637,0.000060672282,0.000015352489,0.000008841705,0.0028910905,0.000053418702,0.00047436834],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9994647,0.00010468885,0.00007137375,0.00012329633,0.00014738651,0.00008858972],"domain_scores_gemma":[0.9989819,0.00047747418,0.00017194019,0.00009443027,0.00010916715,0.0001650522],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00072960096,0.00032600286,0.0006199716,0.0024552108,0.00058393093,0.00093726953,0.00034344764,0.00062639173,0.0017786252],"category_scores_gemma":[0.0020662125,0.00015585539,0.00065218064,0.0010583879,0.00022109869,0.00022654602,0.00041974193,0.00036476945,0.0005344544],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0022164886,0.00025488454,0.2555551,0.00019900543,0.00059000344,0.007672032,0.0005093973,0.0032227954,0.6552948,0.0008164811,0.0020643729,0.0716047],"study_design_scores_gemma":[0.00010708118,0.00042683797,0.8657949,0.000068274334,0.00063100853,0.016046988,0.0005046109,0.030148767,0.077881135,0.0008957156,0.0074384804,0.000056146262],"about_ca_topic_score_codex":0.0026564747,"about_ca_topic_score_gemma":0.007872538,"teacher_disagreement_score":0.0026564747,"about_ca_system_score_codex":0.00026406182,"about_ca_system_score_gemma":0.0003452048,"threshold_uncertainty_score":0.0059500933},"labels":[],"label_agreement":null},{"id":"W2111661868","doi":"10.1038/ng.923","title":"Mutations in GATA2 cause primary lymphedema associated with a predisposition to acute myeloid leukemia (Emberger syndrome)","year":2011,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Congenital heart defects research","field":"Biochemistry, Genetics and Molecular Biology","cited_by":503,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Institute of Infection and Immunity","funders":"British Heart Foundation; National Institute for Health and Care Research; King's College London; King's College Hospital NHS Foundation Trust","keywords":"Haploinsufficiency; Myeloid leukemia; Biology; Lymphedema; Myeloid; GATA2; Allele; Leukemia; Cancer research; Immunology; Haematopoiesis; Genetics; Transcription factor; Gene; Phenotype; Cancer; Breast cancer; Stem cell","score_opus":0.010669332695088388,"score_gpt":0.2645721939017038,"score_spread":0.25390286120661537,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2111661868","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9935002,0.00045528688,0.0016970333,0.00042208147,0.000071842616,0.00005485927,0.00034022945,0.00014751639,0.003310863],"genre_scores_gemma":[0.99799526,0.000111350004,0.0008837038,0.00007207887,0.000055129763,0.000013503793,0.00008422616,0.000024541452,0.00076025655],"study_design_codex":"case_report","study_design_gemma":"observational","domain_scores_codex":[0.9997137,0.000060108647,0.000034133736,0.00005587428,0.00007177164,0.00006449848],"domain_scores_gemma":[0.9994943,0.00016364858,0.0001542569,0.000021544389,0.000017633134,0.00014856514],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00024529884,0.0014134067,0.00043052467,0.00092904986,0.00043837892,0.00033081943,0.0005815199,0.001089988,0.003738305],"category_scores_gemma":[0.00077590917,0.00029566523,0.0004753801,0.00047154975,0.0008641391,0.0002324724,0.0008068437,0.0007867455,0.00057246553],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0009773071,0.00019500096,0.022437738,0.0001942915,0.00016018558,0.5533249,0.0005685344,0.0006041802,0.41060215,0.00209032,0.0015509403,0.0072944625],"study_design_scores_gemma":[0.00044424876,0.00044733187,0.13606812,0.00008179909,0.00037350893,0.7844645,0.00035986278,0.0029353616,0.06842014,0.0009917178,0.00533214,0.00008131608],"about_ca_topic_score_codex":0.0009847498,"about_ca_topic_score_gemma":0.0011585382,"teacher_disagreement_score":0.003738305,"about_ca_system_score_codex":0.0003291772,"about_ca_system_score_gemma":0.00024060182,"threshold_uncertainty_score":0.012505889},"labels":[],"label_agreement":null},{"id":"W2112826900","doi":"10.1038/72877","title":"Localization to Xq27 of a susceptibility gene for testicular germ-cell tumours","year":2000,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Testicular diseases and treatments","field":"Medicine","cited_by":265,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Toronto","funders":"","keywords":"Biology; Testicular cancer; Genetics; Locus (genetics); Chromosome; Cancer; Gene; Gynecology; Medicine","score_opus":0.007466831682472759,"score_gpt":0.2784990801051479,"score_spread":0.27103224842267515,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2112826900","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.98597866,0.0021619883,0.0033756644,0.0011477001,0.00016802379,0.000052110154,0.0005341005,0.00017379463,0.0064079263],"genre_scores_gemma":[0.99505216,0.00046208134,0.00083990546,0.000079535785,0.00008117939,0.000018840701,0.0003019438,0.000029092798,0.0031353596],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9998271,0.0000325247,0.000013980869,0.000051129995,0.00004059342,0.000034722252],"domain_scores_gemma":[0.9995018,0.00016763103,0.0001444458,0.00004172515,0.00004950209,0.00009495536],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00017184316,0.00060897146,0.00051375985,0.001457127,0.0006303957,0.0003765729,0.0006629691,0.0008399652,0.009279207],"category_scores_gemma":[0.0007304995,0.00034822844,0.00053607096,0.00045009475,0.000775534,0.00022964417,0.00048082907,0.0006512565,0.0016103046],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0023405335,0.0002490334,0.032995157,0.0003934819,0.0004692827,0.094334394,0.00078420865,0.001538148,0.83204895,0.0090260105,0.005281946,0.02053882],"study_design_scores_gemma":[0.001033622,0.0014633345,0.30417264,0.00015881204,0.00091810286,0.2142173,0.0015800932,0.0031136468,0.4187963,0.008831779,0.04554766,0.00016663608],"about_ca_topic_score_codex":0.0018540606,"about_ca_topic_score_gemma":0.00133687,"teacher_disagreement_score":0.009279207,"about_ca_system_score_codex":0.00039210476,"about_ca_system_score_gemma":0.0003277611,"threshold_uncertainty_score":0.031042099},"labels":[],"label_agreement":null},{"id":"W2112848098","doi":"10.1038/ng.784","title":"Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease","year":2011,"lang":"en","type":"review","venue":"Nature Genetics","topic":"Genetic Associations and Epidemiology","field":"Biochemistry, Genetics and Molecular Biology","cited_by":1951,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"McGill University; McMaster University; Université de Montréal; Population Health Research Institute; Montreal Heart Institute; Canadian Heart Research Centre; Hamilton Health Sciences; University of Ottawa","funders":"National Heart, Lung, and Blood Institute; Economic and Social Research Council; British Heart Foundation","keywords":"Biology; Coronary artery disease; Genome-wide association study; Genotyping; Genetics; Allele; Genetic association; CAD; Single-nucleotide polymorphism; Bioinformatics; Internal medicine; Gene; Genotype; Medicine","score_opus":0.02046631466090232,"score_gpt":0.3155227776816328,"score_spread":0.29505646302073046,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2112848098","genre_codex":"review","genre_gemma":"review","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"review","genre_consensus":"review","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.00043601706,0.99424696,0.002065284,0.0016413429,0.00040303858,0.000007706995,0.00008179792,0.000036360732,0.001081436],"genre_scores_gemma":[0.0021987988,0.99281704,0.0020488675,0.0011005842,0.0008688003,0.000018203307,0.00017200533,0.0000069784373,0.00076873036],"study_design_codex":"design_other","study_design_gemma":"observational","domain_scores_codex":[0.9994579,0.000100895595,0.000058519323,0.00014338037,0.00020328767,0.00003612388],"domain_scores_gemma":[0.9976852,0.0014518882,0.00021168562,0.00008223012,0.00042138115,0.00014759292],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0024566432,0.0014441059,0.0021071667,0.0016440691,0.00025513847,0.0012479257,0.0015953676,0.0019566696,0.001813735],"category_scores_gemma":[0.0022846947,0.00045638662,0.0005852635,0.0022013246,0.0009785024,0.0010443402,0.00093631,0.0026763566,0.0016866238],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00015661228,0.00007414947,0.0020551302,0.0035857148,0.0002939484,0.00035333773,0.000031414926,0.0003222818,0.0028724496,0.0032358745,0.037146337,0.94987273],"study_design_scores_gemma":[0.00019695054,0.00015908966,0.016169656,0.0033057185,0.0009771872,0.0043092174,0.00010618718,0.00047200787,0.0019010074,0.016230566,0.95606184,0.00011048915],"about_ca_topic_score_codex":0.0012448006,"about_ca_topic_score_gemma":0.0028142114,"teacher_disagreement_score":0.0024566432,"about_ca_system_score_codex":0.00062339095,"about_ca_system_score_gemma":0.0013324172,"threshold_uncertainty_score":0.012992144},"labels":[],"label_agreement":null},{"id":"W2113194569","doi":"10.1038/ng870","title":"Evidence of cis-acting factors in replication-mediated trinucleotide repeat instability in primate cells","year":2002,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Genetic Neurodegenerative Diseases","field":"Neuroscience","cited_by":199,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Toronto; Hospital for Sick Children","funders":"March of Dimes Foundation; National Institutes of Health; Natural Sciences and Engineering Research Council of Canada; Muscular Dystrophy Association; Canadian Institutes of Health Research; Hospital for Sick Children","keywords":"Biology; Okazaki fragments; Trinucleotide repeat expansion; Genetics; DNA replication; Replication timing; Replication (statistics); DNA; Gene; Eukaryotic DNA replication; Allele; Virology","score_opus":0.060001269735899546,"score_gpt":0.3114137742006797,"score_spread":0.2514125044647802,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2113194569","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.96555907,0.006839584,0.014889904,0.00046203335,0.00009717204,0.000068649875,0.00081721,0.00056364044,0.010702767],"genre_scores_gemma":[0.9896988,0.0009935187,0.0048972405,0.0001644993,0.00004068352,0.00004919923,0.0009001397,0.00008417827,0.003171657],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9995746,0.00008352298,0.0000369483,0.00014026166,0.000100226236,0.000064425214],"domain_scores_gemma":[0.9990441,0.00037150097,0.0001264409,0.0002279116,0.000116147814,0.000113821174],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.000450715,0.00038373837,0.00043146982,0.0006714093,0.00086353667,0.0007611615,0.00054380903,0.00084817293,0.003375411],"category_scores_gemma":[0.00097308005,0.00037907888,0.0004032843,0.00029130394,0.00057797716,0.0004221246,0.0005332205,0.0011092351,0.0014670165],"study_design_candidate":"bench_or_experimental","study_design_consensus":"bench_or_experimental","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00012734292,0.000014390314,0.00079040346,0.000034944413,0.000008061926,0.00024893667,0.00009754321,0.000060967683,0.99595815,0.00064922136,0.0000755134,0.0019344683],"study_design_scores_gemma":[0.000023254683,0.0004260725,0.018105011,0.000020776535,0.000053617303,0.0022245075,0.00026890644,0.0012095707,0.96917087,0.0011539075,0.007312842,0.00003077565],"about_ca_topic_score_codex":0.002028747,"about_ca_topic_score_gemma":0.0024217016,"teacher_disagreement_score":0.003375411,"about_ca_system_score_codex":0.0005673673,"about_ca_system_score_gemma":0.00032093556,"threshold_uncertainty_score":0.0112918615},"labels":[],"label_agreement":null},{"id":"W2113764519","doi":"10.1038/ng.519","title":"AHI1 is required for photoreceptor outer segment development and is a modifier for retinal degeneration in nephronophthisis","year":2010,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Genetic and Kidney Cyst Diseases","field":"Biochemistry, Genetics and Molecular Biology","cited_by":189,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"McGill University Health Centre","funders":"National Institute of Diabetes and Digestive and Kidney Diseases; National Institute of General Medical Sciences; National Institute of Neurological Disorders and Stroke; National Eye Institute; European Synchrotron Radiation Facility","keywords":"Ciliopathies; Nephronophthisis; Biology; Ciliopathy; Retinal degeneration; Cilium; Retinitis pigmentosa; Retinal; Retina; Genetics; Opsin; Joubert syndrome; Phenotype; Cell biology; Neuroscience; Gene","score_opus":0.009591904049161175,"score_gpt":0.26232874876125184,"score_spread":0.2527368447120907,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2113764519","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99093187,0.0014084362,0.003552721,0.00040758686,0.00012748908,0.00003240699,0.00082077004,0.00024182981,0.0024768722],"genre_scores_gemma":[0.9960672,0.00029285837,0.0014521363,0.000067084395,0.000025817624,0.000016872038,0.0005298731,0.000064981316,0.0014832165],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.999684,0.00004491191,0.000041310166,0.00006333032,0.00012453884,0.000041956668],"domain_scores_gemma":[0.99951255,0.00010949663,0.00017409807,0.000043215558,0.00003092172,0.00012968446],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00023585543,0.00048595679,0.00040297164,0.0009796824,0.0005636984,0.00045922227,0.0006546267,0.0007471823,0.0022300314],"category_scores_gemma":[0.00044285358,0.0003641217,0.00036128872,0.0003457107,0.00074551906,0.00029699501,0.0005609917,0.0010844556,0.00053481007],"study_design_candidate":"bench_or_experimental","study_design_consensus":"bench_or_experimental","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00029662607,0.000029153825,0.0014405762,0.00003747347,0.000021045405,0.002053853,0.000033233013,0.00020513189,0.9934282,0.00040543338,0.00020680978,0.0018424081],"study_design_scores_gemma":[0.00011296944,0.0001379942,0.057278283,0.00002358806,0.0001034801,0.011305773,0.00012057667,0.0033379185,0.9200992,0.0010381426,0.00640213,0.000040020353],"about_ca_topic_score_codex":0.0012127276,"about_ca_topic_score_gemma":0.0011377356,"teacher_disagreement_score":0.0022300314,"about_ca_system_score_codex":0.0005600773,"about_ca_system_score_gemma":0.0002760134,"threshold_uncertainty_score":0.007460177},"labels":[],"label_agreement":null},{"id":"W2114232003","doi":"10.1038/ng1511","title":"A syndrome of altered cardiovascular, craniofacial, neurocognitive and skeletal development caused by mutations in TGFBR1 or TGFBR2","year":2005,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Connective tissue disorders research","field":"Biochemistry, Genetics and Molecular Biology","cited_by":1778,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"McGill University","funders":"","keywords":"Biology; Craniofacial; Craniosynostosis; Phenotype; Transforming growth factor beta; Allele; Endocrinology; Genetics; Transforming growth factor; Internal medicine; Gene; Medicine","score_opus":0.011789066212639027,"score_gpt":0.28575547712933386,"score_spread":0.2739664109166948,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2114232003","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9373046,0.0036214758,0.015117694,0.0032586057,0.0009991423,0.00044111558,0.0034273516,0.0014186354,0.034411404],"genre_scores_gemma":[0.9786371,0.0010535399,0.0074416837,0.00069295196,0.00054276217,0.00014898002,0.0007453577,0.00020712685,0.010530568],"study_design_codex":"case_report","study_design_gemma":"observational","domain_scores_codex":[0.9992748,0.00010865586,0.00007863169,0.00017253208,0.00024227933,0.00012310222],"domain_scores_gemma":[0.9982621,0.00069958466,0.00043014076,0.00008571221,0.00008800972,0.0004343648],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.000430451,0.0056961523,0.0015292241,0.0027257123,0.0015163269,0.0006964875,0.001474857,0.0031052583,0.0083291195],"category_scores_gemma":[0.0025558795,0.0007586429,0.001113585,0.0018479079,0.0019265458,0.00074021844,0.0018415845,0.0017642665,0.0013337878],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0007644707,0.00010618083,0.0049530664,0.00020355063,0.00021774118,0.88161445,0.00058699446,0.00041898925,0.09795208,0.0027787006,0.0017646147,0.008639249],"study_design_scores_gemma":[0.0003207098,0.0004607452,0.02756731,0.00007434391,0.0003506786,0.94699097,0.00027700726,0.0014966562,0.015658608,0.0013956318,0.005327184,0.00008014183],"about_ca_topic_score_codex":0.0033176942,"about_ca_topic_score_gemma":0.003124633,"teacher_disagreement_score":0.0083291195,"about_ca_system_score_codex":0.00042839197,"about_ca_system_score_gemma":0.0010278176,"threshold_uncertainty_score":0.027863681},"labels":[],"label_agreement":null},{"id":"W2115219137","doi":"10.1038/ng2117","title":"A high-resolution atlas of nucleosome occupancy in yeast","year":2007,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Genomics and Chromatin Dynamics","field":"Biochemistry, Genetics and Molecular Biology","cited_by":856,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Toronto","funders":"","keywords":"Nucleosome; Biology; Occupancy; Genetics; Genome; Saccharomyces cerevisiae; Computational biology; Transcription (linguistics); Gene; Histone; Ecology","score_opus":0.0035346996362735092,"score_gpt":0.22886266666941085,"score_spread":0.22532796703313734,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2115219137","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.87926745,0.0072140703,0.076513335,0.0003896376,0.00011629296,0.00004761983,0.02538626,0.0025422373,0.008523224],"genre_scores_gemma":[0.90245247,0.0031375925,0.062796086,0.00018447373,0.00004306071,0.000061050225,0.024549037,0.00056679785,0.0062094745],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99986994,0.00000836259,0.0000059079894,0.00004359651,0.000045517092,0.000026609807],"domain_scores_gemma":[0.99983597,0.00002573024,0.000017963272,0.000041524385,0.00003559772,0.000043098797],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0001583349,0.00023404989,0.00045041667,0.0009622299,0.0007578582,0.000695898,0.00040539945,0.00031609257,0.0018995039],"category_scores_gemma":[0.00018276194,0.00032780765,0.0003510965,0.0013943671,0.00014742432,0.00028371182,0.00045377595,0.0005437381,0.0007830066],"study_design_candidate":"bench_or_experimental","study_design_consensus":"bench_or_experimental","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00032195152,0.000023749168,0.0026769065,0.00012525397,0.000057750367,0.000100828656,0.00007057742,0.0014117558,0.97760063,0.0006341237,0.0015862552,0.015390085],"study_design_scores_gemma":[0.00008358835,0.00024727054,0.25175613,0.000038680486,0.00021959635,0.0025198236,0.00025756087,0.016104218,0.6646993,0.0026414073,0.06134682,0.00008554782],"about_ca_topic_score_codex":0.0067367973,"about_ca_topic_score_gemma":0.017743902,"teacher_disagreement_score":0.0067367973,"about_ca_system_score_codex":0.00042409834,"about_ca_system_score_gemma":0.00045521633,"threshold_uncertainty_score":0.013395131},"labels":[],"label_agreement":null},{"id":"W2115779804","doi":"10.1038/ng.2802","title":"Meta-analysis of 74,046 individuals identifies 11 new susceptibility loci for Alzheimer's disease","year":2013,"lang":"en","type":"review","venue":"Nature Genetics","topic":"Alzheimer's disease research and treatments","field":"Medicine","cited_by":4659,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Occupational Cancer Research Centre; McGill University and Génome Québec Innovation Centre; University of Toronto","funders":"National Institute of Neurological Disorders and Stroke; National Institute of Diabetes and Digestive and Kidney Diseases; National Human Genome Research Institute; National Heart, Lung, and Blood Institute; National Center for Advancing Translational Sciences; Medical Research Council; Hjartavernd; National Institutes of Health; Karl-Franzens-Universität Graz; Perelman School of Medicine, University of Pennsylvania; Háskóli Íslands; Erasmus Medisch Centrum; Institut National de la Santé et de la Recherche Médicale; Agence Nationale de la Recherche; Versus Arthritis; Cardiff University; National Institute on Aging; National Institute for Health and Care Research; University of Miami; Wellcome Trust; Dr. John T. MacDonald Foundation; Development of Innovative Strategies for a Transdisciplinary approach to ALZheimer's disease; Medizinische Universität Graz; Alzheimer's Association; Llywodraeth Cymru; University of Washington; School of Medicine, Boston University; Vanderbilt University; Universität Zürich; University of Pennsylvania","keywords":"Genome-wide association study; Single-nucleotide polymorphism; Apolipoprotein E; Disease; Biology; Alzheimer's disease; Genetic association; Genetics; Meta-analysis; Locus (genetics); Genotype; Medicine; Gene; Internal medicine","score_opus":0.17758605960259344,"score_gpt":0.42926135966966616,"score_spread":0.2516753000670727,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2115779804","genre_codex":"review","genre_gemma":"review","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"review","genre_consensus":"review","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.009270372,0.9881841,0.0010290524,0.00038893652,0.00018041334,0.000034927925,0.0005135177,0.000027321097,0.0003712559],"genre_scores_gemma":[0.21090724,0.78137094,0.0037210076,0.0013014268,0.00042131997,0.00011829477,0.0015724687,0.00002718038,0.0005600587],"study_design_codex":"meta_analysis","study_design_gemma":"meta_analysis","domain_scores_codex":[0.99814236,0.0007831531,0.00040514529,0.00033800706,0.00024541523,0.00008590109],"domain_scores_gemma":[0.99556655,0.003444637,0.00047672025,0.00020475245,0.00024206143,0.00006514132],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0041806577,0.0022445216,0.005435397,0.0024141576,0.00027699908,0.0008703587,0.0010698844,0.0010544187,0.0022848304],"category_scores_gemma":[0.007770199,0.0007338578,0.01042882,0.0031156777,0.00029387223,0.00067022466,0.00081018085,0.0008405285,0.00023027827],"study_design_candidate":"meta_analysis","study_design_consensus":"meta_analysis","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.006603396,0.00010624432,0.041796327,0.10571936,0.608639,0.00095854164,0.00014587933,0.0011827004,0.0023673698,0.00055796606,0.006361787,0.22556144],"study_design_scores_gemma":[0.0013889688,0.00056104135,0.03988641,0.0069013145,0.9330888,0.0009286272,0.000078447105,0.00024469977,0.0005483491,0.0016299938,0.014683214,0.000060159295],"about_ca_topic_score_codex":0.0029427959,"about_ca_topic_score_gemma":0.010676927,"teacher_disagreement_score":0.005435397,"about_ca_system_score_codex":0.0006681714,"about_ca_system_score_gemma":0.0012922168,"threshold_uncertainty_score":0.022109687},"labels":[],"label_agreement":null},{"id":"W2115783720","doi":"10.1038/ng.582","title":"Genome-wide association study meta-analysis identifies seven new rheumatoid arthritis risk loci","year":2010,"lang":"en","type":"review","venue":"Nature Genetics","topic":"Systemic Lupus Erythematosus Research","field":"Medicine","cited_by":1279,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Toronto; University Health Network; Mount Sinai Hospital","funders":"National Center for Research Resources; National Institute of Arthritis and Musculoskeletal and Skin Diseases; National Institute of Allergy and Infectious Diseases; National Institute for Health and Care Research; Canadian Institutes of Health Research; National Cancer Institute; National Institutes of Health; Versus Arthritis; National Heart, Lung, and Blood Institute","keywords":"Rheumatoid arthritis; Single-nucleotide polymorphism; Genome-wide association study; Biology; Allele; Arthritis; SNP; Genetic association; Genetics; Immunology; Gene; Genotype","score_opus":0.04726879696802014,"score_gpt":0.35946498587530445,"score_spread":0.3121961889072843,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2115783720","genre_codex":"review","genre_gemma":"review","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"review","genre_consensus":"review","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.0016011974,0.9965946,0.0006989908,0.0004982761,0.00013487329,0.000008456353,0.00013532073,0.000019973977,0.00030831114],"genre_scores_gemma":[0.01988315,0.97641957,0.002017803,0.0006563154,0.0003291169,0.000026841883,0.00039889495,0.000007974164,0.0002603457],"study_design_codex":"design_other","study_design_gemma":"meta_analysis","domain_scores_codex":[0.9991443,0.0002606136,0.00013400152,0.00020335474,0.00021064213,0.00004702003],"domain_scores_gemma":[0.99745256,0.0019045338,0.00027542643,0.00008672614,0.00022120248,0.000059650527],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.002612859,0.0018991305,0.0049343994,0.0024460426,0.00023401574,0.0011596594,0.0015821906,0.001204774,0.0017862014],"category_scores_gemma":[0.0036151183,0.0005466158,0.0034612007,0.003283484,0.0003302903,0.0005744983,0.00063892466,0.0011705696,0.00037591258],"study_design_candidate":"meta_analysis","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0021074181,0.000114623275,0.024435772,0.04771495,0.0510191,0.0014828509,0.00010847698,0.0010916634,0.0027093552,0.0012357073,0.017417332,0.85056275],"study_design_scores_gemma":[0.0034639437,0.0013610757,0.16638075,0.028901087,0.43359226,0.013055297,0.00046530564,0.0017439963,0.0050112233,0.014795585,0.33080003,0.0004295382],"about_ca_topic_score_codex":0.0022661758,"about_ca_topic_score_gemma":0.006828536,"teacher_disagreement_score":0.0049343994,"about_ca_system_score_codex":0.0006315952,"about_ca_system_score_gemma":0.0016954013,"threshold_uncertainty_score":0.013818264},"labels":[],"label_agreement":null},{"id":"W2116064842","doi":"10.1038/ng1274","title":"Mutations in HFE2 cause iron overload in chromosome 1q–linked juvenile hemochromatosis","year":2003,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Iron Metabolism and Disorders","field":"Medicine","cited_by":976,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of British Columbia; Xenon Pharmaceuticals (Canada)","funders":"National and Kapodistrian University of Athens; BC Children's Hospital","keywords":"Hepcidin; Biology; HAMP; Hemochromatosis; Ferroportin; Positional cloning; Genetics; Hereditary hemochromatosis; Locus (genetics); Endocrinology; Internal medicine; Gene; Immunology; Medicine","score_opus":0.009449364065446247,"score_gpt":0.27312008869240173,"score_spread":0.2636707246269555,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2116064842","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99716705,0.00017865017,0.0009136365,0.0002439205,0.00005084847,0.000015785974,0.00013429126,0.000045806526,0.0012499727],"genre_scores_gemma":[0.99860877,0.00006221915,0.0003955531,0.000073521274,0.000047723643,0.0000062880295,0.00010458334,0.000020378675,0.0006810952],"study_design_codex":"case_report","study_design_gemma":"observational","domain_scores_codex":[0.9998109,0.000036562957,0.000022333612,0.0000429247,0.000049248814,0.000038095895],"domain_scores_gemma":[0.9994012,0.00028216417,0.00011659905,0.00002398377,0.000046469017,0.00012952749],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0002457326,0.0010750962,0.000417939,0.00078722805,0.00057729526,0.000312589,0.00040449153,0.0014842638,0.0025858164],"category_scores_gemma":[0.0009748399,0.00025504216,0.0004339681,0.0004103383,0.00065074983,0.00023220434,0.0004105821,0.0006267157,0.000445738],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0023606645,0.0003985354,0.052685995,0.00015047993,0.00026717442,0.50268286,0.0014602337,0.0013662763,0.41944686,0.0013546514,0.0034610913,0.014365149],"study_design_scores_gemma":[0.0010862496,0.0006772628,0.35750896,0.00007646722,0.0004621135,0.5064381,0.0011381588,0.005752464,0.11649346,0.0019729096,0.008250943,0.00014295348],"about_ca_topic_score_codex":0.0016852267,"about_ca_topic_score_gemma":0.0019686935,"teacher_disagreement_score":0.0025858164,"about_ca_system_score_codex":0.0003542183,"about_ca_system_score_gemma":0.0001935901,"threshold_uncertainty_score":0.008650482},"labels":[],"label_agreement":null},{"id":"W2116668074","doi":"10.1038/ng.2250","title":"Identification of common variants associated with human hippocampal and intracranial volumes","year":2012,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Genetic Associations and Epidemiology","field":"Biochemistry, Genetics and Molecular Biology","cited_by":660,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"McGill University; SickKids Foundation; Montreal Neurological Institute and Hospital; Hospital for Sick Children; University of Toronto","funders":"National Center for Research Resources; National Institute of Neurological Disorders and Stroke; National Institute of Mental Health; University of California, San Diego; National Institutes of Health; National Institute of Biomedical Imaging and Bioengineering; Canadian Institutes of Health Research; Ipsen; H. Lundbeck A/S; Servier; Bundesministerium für Bildung und Forschung; National Institute on Aging; National Institute for Health and Care Research; Pfizer; Biogen; BioClinica; Bayer HealthCare; Alzheimer's Disease Neuroimaging Initiative; Nederlandse Organisatie voor Wetenschappelijk Onderzoek; Biotechnology and Biological Sciences Research Council; Wellcome Trust; Synarc; Cilag; Medpace; Eisai; Howard Hughes Medical Institute; Genentech; Alexander von Humboldt-Stiftung; Deutsche Forschungsgemeinschaft; Eunice Kennedy Shriver National Institute of Child Health and Human Development; Alzheimer's Drug Discovery Foundation; GlaxoSmithKline; National Center for Advancing Translational Sciences; School of Medicine, University of New Mexico; Cure Alzheimer's Fund; AstraZeneca; U.S. Public Health Service; Eli Lilly and Company; Bristol-Myers Squibb; Siemens; TauRx Pharmaceuticals; Hôpitaux Universitaires de Genève; Alzheimer's Association; Foundation for the National Institutes of Health","keywords":"Hippocampal formation; Brain size; Genome-wide association study; Biology; Locus (genetics); Hippocampus; Magnetic resonance imaging; Human brain; Neuroscience; Single-nucleotide polymorphism; Genetics; Genotype; Gene; Medicine; Radiology","score_opus":0.007762426884572167,"score_gpt":0.2682579960081517,"score_spread":0.2604955691235795,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2116668074","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9971041,0.00065188814,0.0010969624,0.00010501077,0.000020980955,0.0000067478977,0.00048763,0.000029541678,0.00049709727],"genre_scores_gemma":[0.9986846,0.00015360996,0.0006457779,0.00002423838,0.000025221188,0.0000048588026,0.00023096627,0.000015667962,0.00021508004],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99900514,0.00019763422,0.00017501475,0.00034434785,0.00018066609,0.000097118376],"domain_scores_gemma":[0.9974554,0.001036137,0.00085241924,0.00029172676,0.00018186253,0.00018251754],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0006008996,0.00073824066,0.000665349,0.0027952576,0.000626527,0.00089951284,0.0008720385,0.0011098693,0.0030227753],"category_scores_gemma":[0.0026631167,0.00044129815,0.0011914144,0.0029238362,0.0007380184,0.00039088342,0.00068720477,0.000904097,0.00020572396],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.002826786,0.00016323956,0.8808702,0.00016889776,0.0032015694,0.007950844,0.000692385,0.0012140274,0.083324835,0.0014185618,0.00060017465,0.017568378],"study_design_scores_gemma":[0.00010458438,0.00018372889,0.98018014,0.00002830809,0.0011556284,0.00823514,0.00021876999,0.0014405047,0.0063411715,0.0012673376,0.00080690597,0.00003788384],"about_ca_topic_score_codex":0.004989963,"about_ca_topic_score_gemma":0.004029838,"teacher_disagreement_score":0.004989963,"about_ca_system_score_codex":0.00024048323,"about_ca_system_score_gemma":0.00032327278,"threshold_uncertainty_score":0.010112226},"labels":[],"label_agreement":null},{"id":"W2116753165","doi":"10.1038/ng1416","title":"Detection of large-scale variation in the human genome","year":2004,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Genomic variations and chromosomal abnormalities","field":"Biochemistry, Genetics and Molecular Biology","cited_by":2910,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Hospital for Sick Children; University of Toronto","funders":"","keywords":"Biology; Genome; Human genome; Genetics; Structural variation; Phenotype; Gene; Human genetic variation; Copy-number variation; Variation (astronomy); Evolutionary biology","score_opus":0.004407612615571137,"score_gpt":0.22737820150117624,"score_spread":0.22297058888560511,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2116753165","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.973531,0.0032904628,0.016961105,0.0006073185,0.00008660744,0.00002857863,0.0016295824,0.00023949209,0.0036258767],"genre_scores_gemma":[0.99077356,0.00047918732,0.0067710592,0.00024124254,0.000046441128,0.000015708756,0.00076003565,0.000031495463,0.0008813234],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.999796,0.000032808264,0.0000073361894,0.00008709544,0.000056985118,0.000019765066],"domain_scores_gemma":[0.99936634,0.00035259099,0.00009952022,0.00006906528,0.000037858368,0.000074613024],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00021517971,0.0001495053,0.00020376939,0.00062817964,0.0001695735,0.00035284218,0.00019223466,0.0005551478,0.0011313657],"category_scores_gemma":[0.0010228753,0.00017804469,0.0001416293,0.0005843382,0.00030244066,0.00019097043,0.000313248,0.00058403006,0.00030288126],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00026041086,0.000055017183,0.032494057,0.00010612387,0.00011649627,0.0006599636,0.00008699161,0.00048575352,0.9358044,0.001054305,0.0006828132,0.028193733],"study_design_scores_gemma":[0.00007419875,0.0003322807,0.70429826,0.000022916141,0.00016813676,0.0064149313,0.00013504358,0.0036013958,0.2705646,0.0037075467,0.010644822,0.000035962905],"about_ca_topic_score_codex":0.0005292809,"about_ca_topic_score_gemma":0.0010837767,"teacher_disagreement_score":0.0011313657,"about_ca_system_score_codex":0.00012698563,"about_ca_system_score_gemma":0.00011947969,"threshold_uncertainty_score":0.0037847757},"labels":[],"label_agreement":null},{"id":"W2117513049","doi":"10.1038/ng1048","title":"HRPT2, encoding parafibromin, is mutated in hyperparathyroidism–jaw tumor syndrome","year":2002,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Parathyroid Disorders and Treatments","field":"Medicine","cited_by":749,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Mount Sinai Hospital","funders":"","keywords":"Biology; Exon; Germline; Locus (genetics); Germline mutation; Genetics; Gene; Tumor suppressor gene; Mutation; Molecular biology; Cancer research; Carcinogenesis","score_opus":0.016800718614906823,"score_gpt":0.27249590844778837,"score_spread":0.25569518983288153,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2117513049","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9914942,0.001655176,0.0020522673,0.0006506793,0.00013654344,0.00003938722,0.00052612694,0.00014277118,0.0033028563],"genre_scores_gemma":[0.9979061,0.0002536826,0.0007259595,0.00009563183,0.00007900095,0.0000083841305,0.00015172602,0.000020387208,0.0007592229],"study_design_codex":"case_report","study_design_gemma":"observational","domain_scores_codex":[0.9997359,0.00002750587,0.000029972713,0.00007193152,0.000101882775,0.00003287573],"domain_scores_gemma":[0.99958926,0.0001770303,0.0001035583,0.000017166967,0.000025891279,0.00008708665],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00019199029,0.0007816871,0.00044137114,0.0010163612,0.0005074418,0.000488799,0.0004016466,0.001751131,0.0018696452],"category_scores_gemma":[0.0008292261,0.00027350045,0.00044647433,0.0006408219,0.0006009037,0.00029845512,0.00037076938,0.0005979061,0.00044156806],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0012867745,0.00009549482,0.025474789,0.00018923804,0.00014731487,0.5620559,0.00052693434,0.00062225387,0.39539316,0.001016346,0.001425193,0.0117666125],"study_design_scores_gemma":[0.0002859548,0.00030634616,0.089945614,0.000034656623,0.00036635684,0.80407435,0.00023271072,0.0027499334,0.093330145,0.0011014771,0.007518757,0.0000537205],"about_ca_topic_score_codex":0.0011021071,"about_ca_topic_score_gemma":0.000666566,"teacher_disagreement_score":0.0018696452,"about_ca_system_score_codex":0.0003867856,"about_ca_system_score_gemma":0.00023868571,"threshold_uncertainty_score":0.0062546134},"labels":[],"label_agreement":null},{"id":"W2117733752","doi":"10.1038/72769","title":"ARSACS, a spastic ataxia common in northeastern Québec, is caused by mutations in a new gene encoding an 11.5-kb ORF","year":2000,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Heat shock proteins research","field":"Biochemistry, Genetics and Molecular Biology","cited_by":436,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":true,"ca_institutions":"McGill University; Cégep de Chicoutimi; Hôpital de l'Enfant-Jésus; McGill Genome Centre; Université de Montréal; McGill University Health Centre","funders":"","keywords":"Biology; Genetics; Gene; Exon; Open reading frame; Haplotype; Coding region; Allele; Peptide sequence","score_opus":0.01219439224062585,"score_gpt":0.29351083115712473,"score_spread":0.2813164389164989,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2117733752","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9564706,0.001955101,0.005532354,0.0008805765,0.00028388377,0.0003712793,0.012945624,0.0006697549,0.020890761],"genre_scores_gemma":[0.9681277,0.0008395678,0.0049231187,0.00046881824,0.000054669323,0.00010435719,0.0048003527,0.00008773504,0.020593656],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.99977607,0.00001792137,0.000017693063,0.00005036777,0.00008106846,0.00005701453],"domain_scores_gemma":[0.99946874,0.000079711484,0.00012127687,0.000016625621,0.0001798297,0.00013390166],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00025248915,0.0013512077,0.00041943535,0.0017087554,0.0020518524,0.0005032005,0.00079762895,0.00054748106,0.0063707866],"category_scores_gemma":[0.0006324487,0.00019818194,0.0005701182,0.0015293427,0.0011425677,0.00016555378,0.00046066975,0.0005021739,0.0007717075],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":true,"about_ca_topic_consensus":true,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0024906592,0.00066475116,0.29406717,0.0010531723,0.0010497258,0.06730276,0.0045931893,0.00436235,0.3747069,0.006790609,0.035403326,0.20751551],"study_design_scores_gemma":[0.00042908266,0.00047745122,0.8604223,0.00034756656,0.0005891526,0.017770067,0.0019127268,0.0051105204,0.01638345,0.0009629377,0.0953789,0.0002158481],"about_ca_topic_score_codex":0.8439436,"about_ca_topic_score_gemma":0.9154452,"teacher_disagreement_score":0.1560564,"about_ca_system_score_codex":0.0054661836,"about_ca_system_score_gemma":0.0063124467,"threshold_uncertainty_score":0.31395084},"labels":[],"label_agreement":null},{"id":"W2117910394","doi":"10.1038/ng.3013","title":"Ordering of mutations in preinvasive disease stages of esophageal carcinogenesis","year":2014,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Esophageal Cancer Research and Treatment","field":"Medicine","cited_by":356,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"BC Cancer Agency","funders":"Medical Research Council; National Institute for Health and Care Research; Cancer Research UK; Wellcome Trust","keywords":"Barrett's esophagus; Biology; Dysplasia; Carcinogenesis; Esophagus; Adenocarcinoma; Genetics; Gene; Mutation; Cancer; Cancer research","score_opus":0.01360522482933418,"score_gpt":0.30985469110261943,"score_spread":0.29624946627328524,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2117910394","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9915882,0.0013648991,0.00097014644,0.00014476007,0.000040734994,0.000025170884,0.001348384,0.00007196667,0.0044457424],"genre_scores_gemma":[0.99579513,0.0004065058,0.0012808644,0.00006528359,0.000030205907,0.000009117275,0.00085490244,0.00004325839,0.0015147164],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99929893,0.00015773994,0.00011018105,0.00009725521,0.00016988078,0.00016601387],"domain_scores_gemma":[0.99689156,0.0012642187,0.0005269508,0.00020876469,0.00052867405,0.00057984603],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00042147745,0.00040289483,0.00047792448,0.0037517012,0.0006214834,0.0010496371,0.00036186422,0.0006815263,0.0059447624],"category_scores_gemma":[0.0027011351,0.0002928402,0.0005190468,0.0013734965,0.000380836,0.00045279902,0.0003714616,0.0005722411,0.0010933898],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0035497781,0.00014296618,0.84265643,0.00017426423,0.00018827619,0.002221153,0.00040159613,0.0011823474,0.11739166,0.0016600904,0.0014170075,0.029014375],"study_design_scores_gemma":[0.000044105716,0.0004497616,0.97649604,0.000041656946,0.0001609139,0.0036389248,0.00032610886,0.0017293515,0.012522896,0.0011920867,0.003372088,0.00002610781],"about_ca_topic_score_codex":0.002495911,"about_ca_topic_score_gemma":0.0048567606,"teacher_disagreement_score":0.0059447624,"about_ca_system_score_codex":0.0004763551,"about_ca_system_score_gemma":0.00043483957,"threshold_uncertainty_score":0.019887209},"labels":[],"label_agreement":null},{"id":"W2118286472","doi":"10.1038/ng.3122","title":"Mutations in PLK4, encoding a master regulator of centriole biogenesis, cause microcephaly, growth failure and retinopathy","year":2014,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Microtubule and mitosis dynamics","field":"Biochemistry, Genetics and Molecular Biology","cited_by":183,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Hospital for Sick Children; University of Toronto","funders":"Academy of Medical Sciences; National Institute for Health and Care Research; Wellcome Trust","keywords":"Ciliogenesis; Biology; Centriole; Microcephaly; Cilium; Ciliopathies; Genetics; Biogenesis; Phenotype; Regulator; Gene; Cell biology; Microtubule","score_opus":0.0046318662255862815,"score_gpt":0.21594194102968653,"score_spread":0.21131007480410025,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2118286472","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9857831,0.00091687724,0.007463478,0.0006454342,0.00019657091,0.000065046006,0.0018610179,0.00063312904,0.002435231],"genre_scores_gemma":[0.99292856,0.00043984794,0.003179432,0.000089756315,0.000047369893,0.000041048,0.0005511701,0.000119842116,0.0026029851],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99967134,0.00004497259,0.000038388083,0.000070721726,0.00013305446,0.000041466665],"domain_scores_gemma":[0.99891543,0.00030739896,0.00040617547,0.000047315505,0.0000441489,0.0002794605],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00018115138,0.0018983643,0.00045228028,0.0017114931,0.0006070692,0.0003889107,0.00063509285,0.0009848324,0.002017361],"category_scores_gemma":[0.0008004877,0.00039275122,0.000512636,0.0006152874,0.0014906845,0.0002699307,0.00093354273,0.0009865307,0.0003891651],"study_design_candidate":"bench_or_experimental","study_design_consensus":"bench_or_experimental","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.001488637,0.00013437144,0.007126219,0.00019997395,0.0002218929,0.026712226,0.00018076584,0.00380826,0.94536996,0.0018912245,0.0018952925,0.010971205],"study_design_scores_gemma":[0.000583065,0.0006783323,0.10013178,0.00010930326,0.0005332503,0.069124766,0.00042929561,0.017539935,0.79720676,0.0028315836,0.0106370775,0.00019485898],"about_ca_topic_score_codex":0.0027786752,"about_ca_topic_score_gemma":0.0033475095,"teacher_disagreement_score":0.0027786752,"about_ca_system_score_codex":0.00088399334,"about_ca_system_score_gemma":0.0006539517,"threshold_uncertainty_score":0.0067486763},"labels":[],"label_agreement":null},{"id":"W2118434625","doi":"10.1038/ng.513","title":"Genome-wide association study of ankylosing spondylitis identifies non-MHC susceptibility loci","year":2010,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Spondyloarthritis Studies and Treatments","field":"Medicine","cited_by":668,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Alberta; University of Toronto","funders":"National Center for Research Resources; National Institute of Arthritis and Musculoskeletal and Skin Diseases; National Institutes of Health; Versus Arthritis; U.S. Public Health Service; Wellcome Trust","keywords":"Biology; Ankylosing spondylitis; Genome-wide association study; Genetics; Spondylitis; Genetic association; Major histocompatibility complex; Computational biology; Single-nucleotide polymorphism; Immunology; Genotype; Gene","score_opus":0.00782674407337541,"score_gpt":0.27602289954594966,"score_spread":0.26819615547257425,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2118434625","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9966192,0.0013264539,0.00059579837,0.000302971,0.000045509554,0.000005499532,0.00039956564,0.000019297195,0.00068558153],"genre_scores_gemma":[0.99824536,0.00036702727,0.0005230967,0.00006429672,0.000045258847,0.000005526712,0.00025069472,0.000009593407,0.0004891667],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9990429,0.00042312377,0.000087877204,0.00023827274,0.000125931,0.00008190345],"domain_scores_gemma":[0.9986975,0.00054884504,0.00032606974,0.00013932769,0.000103211256,0.000185014],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0011103944,0.00051609025,0.0004689331,0.00120665,0.0006338581,0.0006484283,0.0005738788,0.0006948066,0.0021226893],"category_scores_gemma":[0.0017270081,0.00030909714,0.0006910356,0.0015239032,0.00047193762,0.0002192921,0.00049467065,0.000897551,0.0002297815],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.004760608,0.00029210703,0.92371297,0.00013061917,0.0032359771,0.001478266,0.00026446584,0.0002686585,0.049237207,0.0004883804,0.0013406882,0.014790007],"study_design_scores_gemma":[0.00012222289,0.00016432606,0.9957058,0.000010804452,0.00067755935,0.00096320675,0.00010954809,0.0003357995,0.001029011,0.00029092634,0.00058174867,0.000009146214],"about_ca_topic_score_codex":0.0029068193,"about_ca_topic_score_gemma":0.004826393,"teacher_disagreement_score":0.0029068193,"about_ca_system_score_codex":0.00019945127,"about_ca_system_score_gemma":0.0003134401,"threshold_uncertainty_score":0.0071011186},"labels":[],"label_agreement":null},{"id":"W2118617708","doi":"10.1038/ng1814","title":"Mutations in the gene encoding GlyT2 (SLC6A5) define a presynaptic component of human startle disease","year":2006,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Ion channel regulation and function","field":"Biochemistry, Genetics and Molecular Biology","cited_by":236,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Children's & Women's Health Centre of British Columbia; University of British Columbia; Children's Hospital of Eastern Ontario","funders":"Key Laboratory of Low-grade Energy Utilization Technology and System, Chongqing University","keywords":"Glycine receptor; Missense mutation; Biology; Frameshift mutation; Genetics; Gephyrin; Nonsense mutation; Mutation; Neuroscience; Gene; Glycine; Amino acid","score_opus":0.010532451233335011,"score_gpt":0.2566951501298532,"score_spread":0.2461626988965182,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2118617708","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9962309,0.0003142845,0.0023362066,0.00007533079,0.000015917254,0.000014366662,0.00015653759,0.000041397634,0.0008150924],"genre_scores_gemma":[0.99799275,0.00012151054,0.0013070455,0.000042690266,0.000012687374,0.000004601158,0.00014834011,0.000011179849,0.00035922043],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9999045,0.0000131253,0.000011954324,0.000025174235,0.00003264145,0.00001258032],"domain_scores_gemma":[0.9998312,0.00002915735,0.00006709725,0.000006777267,0.000014248955,0.000051459625],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00009833617,0.0006421675,0.0002565557,0.00040624748,0.00023612523,0.00025730312,0.00017971346,0.0005702453,0.0010402134],"category_scores_gemma":[0.00031545496,0.00013103917,0.00021440188,0.0002938762,0.0003940905,0.00020443457,0.00044959606,0.00034386013,0.00024595574],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0008028425,0.00005237537,0.02607059,0.00009455273,0.00007886566,0.024172736,0.00029385093,0.0008803594,0.9396611,0.0012785946,0.00047340317,0.0061407518],"study_design_scores_gemma":[0.00027728296,0.0011785828,0.4966411,0.00009180318,0.00039560968,0.14778058,0.00078575447,0.010826678,0.33100012,0.002979785,0.00793811,0.00010451558],"about_ca_topic_score_codex":0.0011443169,"about_ca_topic_score_gemma":0.0018981212,"teacher_disagreement_score":0.0011443169,"about_ca_system_score_codex":0.0001835779,"about_ca_system_score_gemma":0.00014395893,"threshold_uncertainty_score":0.003479898},"labels":[],"label_agreement":null},{"id":"W2118899477","doi":"10.1038/ng.2439","title":"CSK regulatory polymorphism is associated with systemic lupus erythematosus and influences B-cell signaling and activation","year":2012,"lang":"en","type":"article","venue":"Nature Genetics","topic":"T-cell and B-cell Immunology","field":"Immunology and Microbiology","cited_by":112,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"McGill University Health Centre","funders":"National Institute of Arthritis and Musculoskeletal and Skin Diseases; National Institute of Allergy and Infectious Diseases; National Center for Research Resources; National Institute of General Medical Sciences","keywords":"LYN; Tyrosine-protein kinase CSK; PTPN22; Biology; Src family kinase; Lupus erythematosus; Tyrosine kinase; Immunology; Systemic lupus erythematosus; Molecular biology; Signal transduction; Cell biology; Single-nucleotide polymorphism; Internal medicine; Genetics; Genotype; Antibody; Gene; Medicine; SH3 domain","score_opus":0.00704448398646388,"score_gpt":0.20504211657510507,"score_spread":0.1979976325886412,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2118899477","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9982652,0.00015613936,0.0006271457,0.00010245798,0.000026875832,0.000007126305,0.00017788785,0.000040689687,0.0005964498],"genre_scores_gemma":[0.99868256,0.000058733473,0.00045887742,0.000047839723,0.00003930781,0.0000062452536,0.0001347277,0.000036839323,0.00053495495],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9993568,0.00020174007,0.000093323135,0.00017445734,0.00009121227,0.00008245955],"domain_scores_gemma":[0.99833965,0.00052917044,0.0006029307,0.00011275325,0.000081240934,0.00033425723],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00040207146,0.0010287111,0.0004692683,0.0014901118,0.00044145004,0.00044103005,0.0005332629,0.000772614,0.006669708],"category_scores_gemma":[0.0009849379,0.0002747851,0.00060622767,0.0010464919,0.00048589724,0.0002137151,0.0002869717,0.0007156279,0.00061337743],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.014561112,0.00077054795,0.2081799,0.00015941651,0.0007930533,0.006038862,0.00033536466,0.0005750853,0.75501513,0.0012618192,0.00074976333,0.011559929],"study_design_scores_gemma":[0.0007203159,0.001219767,0.90719694,0.00009237179,0.00094574905,0.019986711,0.00025687204,0.00400299,0.061371364,0.0012170272,0.0028756608,0.000114372204],"about_ca_topic_score_codex":0.0011596383,"about_ca_topic_score_gemma":0.00086804305,"teacher_disagreement_score":0.006669708,"about_ca_system_score_codex":0.0002640764,"about_ca_system_score_gemma":0.00023166035,"threshold_uncertainty_score":0.022312343},"labels":[],"label_agreement":null},{"id":"W2119258755","doi":"10.1038/ng.2524","title":"A heterozygous moth genome provides insights into herbivory and detoxification","year":2013,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Insect Resistance and Genetics","field":"Biochemistry, Genetics and Molecular Biology","cited_by":578,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Toronto; University of British Columbia; Brock University","funders":"Biotechnology and Biological Sciences Research Council; National Natural Science Foundation of China; Fujian Agriculture and Forestry University; Aarhus Universitet","keywords":"Biology; Diamondback moth; Herbivore; Plutella; Adaptation (eye); Insect; Evolutionary biology; Genome; Detoxification (alternative medicine); Gene; Genetics; Ecology; Lepidoptera genitalia","score_opus":0.0033689551912434368,"score_gpt":0.21677935637467205,"score_spread":0.2134104011834286,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2119258755","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.8295392,0.022067431,0.05358737,0.002403121,0.0008205728,0.00016533406,0.073120914,0.0025306498,0.015765449],"genre_scores_gemma":[0.80169463,0.014130501,0.076720275,0.0010208667,0.00022039379,0.00011280761,0.09182116,0.00060055166,0.0136788925],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99991214,0.0000065298523,0.000005469154,0.00003288234,0.000028628783,0.000014324326],"domain_scores_gemma":[0.99986947,0.000024409836,0.000023969003,0.000019081528,0.000025208525,0.00003795789],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00014865452,0.0006098238,0.0003571645,0.00062200014,0.0003341556,0.00052199315,0.00024077507,0.00055508746,0.0026822367],"category_scores_gemma":[0.00023357794,0.00029836068,0.0006924437,0.0005634248,0.00012554397,0.0003411259,0.00040655,0.0008532384,0.0012468992],"study_design_candidate":"bench_or_experimental","study_design_consensus":"bench_or_experimental","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00040835718,0.000025190328,0.0027084115,0.00033929455,0.000071947776,0.00043290242,0.000096295495,0.00024083852,0.96927285,0.0005774099,0.001642192,0.024184283],"study_design_scores_gemma":[0.00020668049,0.00048810657,0.1925011,0.00028474018,0.00074864103,0.006938445,0.0004361931,0.007119299,0.51796037,0.0047875913,0.26834437,0.00018438674],"about_ca_topic_score_codex":0.0015928843,"about_ca_topic_score_gemma":0.003191166,"teacher_disagreement_score":0.0026822367,"about_ca_system_score_codex":0.00027103288,"about_ca_system_score_gemma":0.000269122,"threshold_uncertainty_score":0.008973002},"labels":[],"label_agreement":null},{"id":"W2120419610","doi":"10.1038/ng.2214","title":"Whole-genome analysis of diverse Chlamydia trachomatis strains identifies phylogenetic relationships masked by current clinical typing","year":2012,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Reproductive tract infections research","field":"Immunology and Microbiology","cited_by":312,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"BC Centre for Disease Control","funders":"National Institute for Health and Care Research; Wellcome Trust","keywords":"Biology; Chlamydia trachomatis; Lymphogranuloma venereum; Phylogenetic tree; Trachoma; Genetics; Phylogenetics; Multilocus sequence typing; Genome; Whole genome sequencing; Chlamydiaceae; Evolutionary biology; Virology; Computational biology; Genotype; Gene","score_opus":0.06388679883420732,"score_gpt":0.37268154881721427,"score_spread":0.30879474998300693,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2120419610","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99516255,0.00068169826,0.0012162457,0.00013728894,0.000016903221,0.000006497082,0.0022536004,0.000038009548,0.00048723488],"genre_scores_gemma":[0.9933609,0.00038253498,0.002005799,0.00019060877,0.0000145986505,0.00000581419,0.003719904,0.00003391842,0.00028586353],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.99970764,0.000044289547,0.000017991653,0.00009864975,0.000053325406,0.000078116114],"domain_scores_gemma":[0.9994456,0.00017703188,0.0001316931,0.00007399872,0.00006328975,0.00010837441],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00033108384,0.0003063485,0.00039240092,0.00093978987,0.0004431251,0.0007056355,0.00025990081,0.00057497766,0.0010783235],"category_scores_gemma":[0.00084286154,0.0001805239,0.0004201178,0.0013206814,0.00029414217,0.00029433658,0.0004706983,0.0007142278,0.00028661898],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0008329813,0.000105344654,0.14868431,0.0001558545,0.0003002715,0.00018678834,0.00046139845,0.00029509593,0.8296379,0.00018725546,0.0005803361,0.018572507],"study_design_scores_gemma":[0.00001179388,0.00015086465,0.98125345,0.000021945141,0.00017021949,0.00075473415,0.00041246245,0.001090997,0.013573308,0.00021522459,0.0023304652,0.00001458123],"about_ca_topic_score_codex":0.002222286,"about_ca_topic_score_gemma":0.005602261,"teacher_disagreement_score":0.002222286,"about_ca_system_score_codex":0.00019901682,"about_ca_system_score_gemma":0.00025135162,"threshold_uncertainty_score":0.0044187307},"labels":[],"label_agreement":null},{"id":"W2122016967","doi":"10.1038/ng.2657","title":"The duck genome and transcriptome provide insight into an avian influenza virus reservoir species","year":2013,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Influenza Virus Research Studies","field":"Medicine","cited_by":460,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Alberta","funders":"Biotechnology and Biological Sciences Research Council; Wellcome Trust","keywords":"Biology; Transcriptome; Goose; Genome; Influenza A virus subtype H5N1; Anas; Gene; Influenza A virus; Host (biology); Virus; Virology; Genetics; Gene expression; Ecology","score_opus":0.04294153144806914,"score_gpt":0.34049668359942664,"score_spread":0.2975551521513575,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2122016967","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.974308,0.0028704815,0.0045624534,0.0006715195,0.00009333493,0.000022902961,0.011450405,0.00016410749,0.0058566616],"genre_scores_gemma":[0.9591079,0.0025494345,0.014513612,0.00043394748,0.00004864444,0.000024774168,0.016993895,0.000094161944,0.0062336633],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.99994266,0.0000035465441,0.0000041492217,0.00002773892,0.000010474905,0.000011433153],"domain_scores_gemma":[0.9998815,0.000018488396,0.000023938062,0.000015501646,0.00003040075,0.00003018014],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00008626357,0.00021398749,0.00022221096,0.00031850868,0.0002696979,0.0004705404,0.00010649272,0.00025511245,0.0013651865],"category_scores_gemma":[0.00013785389,0.00013739681,0.00023416507,0.00029026542,0.00012960994,0.00029502012,0.0002547928,0.00039195508,0.0004555751],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0002901841,0.000021226568,0.036057927,0.00018921669,0.000053138,0.00038848407,0.0004861081,0.00040692344,0.93293744,0.00039455254,0.0015668741,0.02720794],"study_design_scores_gemma":[0.000015106042,0.00015945676,0.8224791,0.000099737925,0.00018679294,0.0015677823,0.0013276448,0.003164752,0.08452012,0.0010931605,0.085328706,0.000057570003],"about_ca_topic_score_codex":0.0045473333,"about_ca_topic_score_gemma":0.010402883,"teacher_disagreement_score":0.0045473333,"about_ca_system_score_codex":0.00038272695,"about_ca_system_score_gemma":0.00023809067,"threshold_uncertainty_score":0.009041727},"labels":[],"label_agreement":null},{"id":"W2122031852","doi":"10.1038/ng2032","title":"Genome-wide association study identifies new susceptibility loci for Crohn disease and implicates autophagy in disease pathogenesis","year":2007,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Inflammatory Bowel Disease","field":"Biochemistry, Genetics and Molecular Biology","cited_by":1751,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Toronto; Hôtel-Dieu de Montréal; Mount Sinai Hospital; Université de Montréal; Hospital for Sick Children; Montreal Heart Institute","funders":"National Institute of Diabetes and Digestive and Kidney Diseases; National Institute of Allergy and Infectious Diseases; Cedars-Sinai Medical Center","keywords":"ATG16L1; Biology; Autophagy; Pathogenesis; Genetics; Disease; Genome-wide association study; Crohn's disease; Gene; Genome; Gene knockdown; Inflammatory bowel disease; Immunology; Single-nucleotide polymorphism; Genotype","score_opus":0.006254114487951199,"score_gpt":0.2650976711601485,"score_spread":0.2588435566721973,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2122031852","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9963355,0.0013324528,0.0011041877,0.0002917621,0.000040529238,0.0000068381355,0.00032640048,0.000035952555,0.0005263917],"genre_scores_gemma":[0.99790335,0.00047039686,0.00090672064,0.000073121664,0.000041049152,0.000007830633,0.00028278356,0.000015672973,0.0002990301],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99944943,0.00017077629,0.00006243785,0.00017461934,0.00008865369,0.00005403401],"domain_scores_gemma":[0.9987275,0.0004476301,0.00035724926,0.0001207421,0.0001009248,0.00024583374],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0009312557,0.00061891245,0.00066313776,0.0021164527,0.0006701947,0.0006202556,0.00043964738,0.00088444276,0.0021813584],"category_scores_gemma":[0.0011623878,0.00037910944,0.0008187403,0.0017381426,0.00058020203,0.00026057198,0.0005443982,0.0009399429,0.00021657173],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0064316187,0.00035288942,0.82249665,0.00016522229,0.002467053,0.0031211867,0.0002628645,0.0003596922,0.1493057,0.00068346533,0.0010611448,0.0132924225],"study_design_scores_gemma":[0.000155395,0.00026263215,0.9894782,0.000016515645,0.00088892656,0.0031614383,0.00012683043,0.00064890407,0.0038083636,0.0005774354,0.0008560589,0.000019363904],"about_ca_topic_score_codex":0.0013221243,"about_ca_topic_score_gemma":0.0021240432,"teacher_disagreement_score":0.0021813584,"about_ca_system_score_codex":0.00021813845,"about_ca_system_score_gemma":0.00025674707,"threshold_uncertainty_score":0.007297337},"labels":[],"label_agreement":null},{"id":"W2122039687","doi":"10.1038/ng.133","title":"Genome-wide association scan identifies a colorectal cancer susceptibility locus on 11q23 and replicates risk loci at 8q24 and 18q21","year":2008,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Genetic factors in colorectal cancer","field":"Medicine","cited_by":604,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Mount Sinai Hospital; Ontario Institute for Cancer Research; Toronto Public Health; Cancer Care Ontario; McGill University and Génome Québec Innovation Centre; Public Health Ontario; Hospital for Sick Children; University of Ottawa","funders":"Medical Research Council; Instituto de Salud Carlos III; Universität Greifswald; Bundesministerium für Bildung und Forschung; Deutsches Krebsforschungszentrum; Deutsche Forschungsgemeinschaft; Scottish Funding Council; National Cancer Institute; Cancer Research UK; Wellcome Trust","keywords":"Biology; Locus (genetics); Genome-wide association study; Genetics; Colorectal cancer; Cancer; Single-nucleotide polymorphism; Gene; Genotype","score_opus":0.01025374827253222,"score_gpt":0.2671343412642006,"score_spread":0.2568805929916684,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2122039687","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9949555,0.0011133103,0.0013541111,0.0005676835,0.00004977963,0.000017443359,0.00088178716,0.00007495605,0.0009854258],"genre_scores_gemma":[0.9965836,0.00036089023,0.0015868861,0.00009106199,0.000051892144,0.000018643887,0.0005251796,0.000016323156,0.00076541834],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9993812,0.00015243246,0.00004381397,0.00020380839,0.00012676917,0.00009199303],"domain_scores_gemma":[0.99777824,0.0010121295,0.0006264244,0.000102290775,0.00016810268,0.0003127767],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00078017934,0.00069815415,0.0007920465,0.0027626676,0.0009621489,0.00067954324,0.000941752,0.001027039,0.0058741756],"category_scores_gemma":[0.0028131306,0.0004519202,0.0008285397,0.0023944254,0.00062146183,0.0002616998,0.0006312049,0.0008881243,0.000354533],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.004134392,0.00021224281,0.9099734,0.00015956795,0.0017730567,0.0071275462,0.0003967368,0.0005867085,0.04907526,0.0005428065,0.0019863583,0.024032002],"study_design_scores_gemma":[0.0003199663,0.00030484292,0.9845206,0.00003602509,0.0014060698,0.0052058063,0.0002506711,0.0008399486,0.0036357343,0.00072869,0.0027235157,0.000028071168],"about_ca_topic_score_codex":0.00655109,"about_ca_topic_score_gemma":0.011966452,"teacher_disagreement_score":0.00655109,"about_ca_system_score_codex":0.00035105486,"about_ca_system_score_gemma":0.0003950881,"threshold_uncertainty_score":0.019651115},"labels":[],"label_agreement":null},{"id":"W2122484762","doi":"10.1038/ng.785","title":"Systematic documentation and analysis of human genetic variation in hemoglobinopathies using the microattribution approach","year":2011,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Hemoglobinopathies and Related Disorders","field":"Medicine","cited_by":161,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"McMaster University; Hamilton Regional Laboratory Medicine Program","funders":"National Institute on Minority Health and Health Disparities; National Human Genome Research Institute; National Institutes of Health; Nederlandse Organisatie voor Wetenschappelijk Onderzoek; National Institute of Allergy and Infectious Diseases; European Commission; National Institute of Diabetes and Digestive and Kidney Diseases; National Heart, Lung, and Blood Institute; Landsteiner Foundation for Blood Transfusion Research","keywords":"Biology; Documentation; Genetic variation; Variation (astronomy); Human genetic variation; Genetics; Gene; Computational biology; Thalassemia; ENCODE; Human genome; Computer science; Genome","score_opus":0.015585684162771837,"score_gpt":0.2680442506372454,"score_spread":0.25245856647447357,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2122484762","genre_codex":"methods","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":null,"domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.13963123,0.0045621605,0.78809756,0.016686931,0.00075022667,0.0017549095,0.013493074,0.014619835,0.020404039],"genre_scores_gemma":[0.2780956,0.0020631233,0.7044651,0.0014185861,0.00029385506,0.0010693253,0.0069426754,0.0012365786,0.004415176],"study_design_codex":"design_other","study_design_gemma":"observational","domain_scores_codex":[0.9537814,0.025968729,0.008125233,0.0039971285,0.0076413187,0.00048619023],"domain_scores_gemma":[0.7292111,0.107580714,0.030976305,0.099877045,0.02882169,0.0035332066],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.04462339,0.00051018037,0.000739196,0.019161247,0.0016080178,0.0067688115,0.0022310843,0.000898226,0.0027003272],"category_scores_gemma":[0.12348551,0.0007861674,0.0005830976,0.012335833,0.0017688915,0.0064735655,0.008169185,0.0015920663,0.001286581],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00046442053,0.00033139734,0.09721087,0.0014538957,0.00039630287,0.0012832917,0.01972273,0.0039230096,0.012278746,0.06283191,0.03682197,0.76328146],"study_design_scores_gemma":[0.00029832646,0.0004215616,0.08008223,0.003349487,0.00053679105,0.0041996217,0.01326772,0.045858923,0.06977376,0.15953994,0.6218966,0.0007749602],"about_ca_topic_score_codex":0.004221938,"about_ca_topic_score_gemma":0.006538457,"teacher_disagreement_score":0.04462339,"about_ca_system_score_codex":0.0024072954,"about_ca_system_score_gemma":0.007733774,"threshold_uncertainty_score":0.23599386},"labels":[],"label_agreement":null},{"id":"W2122621644","doi":"10.1038/ng.285","title":"Common variants in the NLRP3 region contribute to Crohn's disease susceptibility","year":2008,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Inflammasome and immune disorders","field":"Biochemistry, Genetics and Molecular Biology","cited_by":523,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Montreal Heart Institute; Toronto Western Hospital; Centre Hospitalier Universitaire de Sherbrooke; Royal Victoria Regional Health Centre; Université de Montréal; Université du Québec à Chicoutimi; Mount Sinai Hospital; McGill University Health Centre; Royal Victoria Hospital; University of Toronto; Ontario Institute for Cancer Research; McGill University and Génome Québec Innovation Centre; Jewish General Hospital; Montreal General Hospital","funders":"National Institute of Diabetes and Digestive and Kidney Diseases; National Institute of Allergy and Infectious Diseases","keywords":"Single-nucleotide polymorphism; Biology; Odds ratio; Genetics; Crohn's disease; Disease; ATG16L1; Genome-wide association study; Case-control study; Inflammatory bowel disease; Genotype; Gene; Medicine; Internal medicine","score_opus":0.007972779966945884,"score_gpt":0.24941148050817805,"score_spread":0.24143870054123218,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2122621644","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99476904,0.0011208127,0.002022322,0.0003750591,0.00005300189,0.000019169542,0.0004473771,0.00006858837,0.0011246427],"genre_scores_gemma":[0.9984067,0.00018853978,0.00094124634,0.00006829989,0.000038285227,0.0000055953715,0.00010479967,0.000014206514,0.00023226823],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.99955636,0.000118157426,0.00006943547,0.00012281696,0.000079991034,0.000053186868],"domain_scores_gemma":[0.99895346,0.0004471615,0.0003278082,0.00008038965,0.00006475075,0.00012631167],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0004030414,0.0007854507,0.00062596204,0.00090993376,0.00044487242,0.00041675943,0.00035056725,0.0014064454,0.0030285115],"category_scores_gemma":[0.001366738,0.00028295058,0.00079048076,0.00094557984,0.00044591434,0.00022707367,0.00031813176,0.00073803036,0.0003386214],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.011376982,0.00035382484,0.33355802,0.00034999923,0.0015996108,0.042117495,0.0009855602,0.0027081221,0.57131624,0.0034752619,0.0020130533,0.030145757],"study_design_scores_gemma":[0.0008230544,0.00059078325,0.857427,0.0001667352,0.0018519448,0.08003517,0.0005095684,0.0048022904,0.042436976,0.006368739,0.0048718248,0.00011588798],"about_ca_topic_score_codex":0.0010841066,"about_ca_topic_score_gemma":0.00082921854,"teacher_disagreement_score":0.0030285115,"about_ca_system_score_codex":0.0002610397,"about_ca_system_score_gemma":0.00019912749,"threshold_uncertainty_score":0.010131359},"labels":[],"label_agreement":null},{"id":"W2122791877","doi":"10.1038/ng.572","title":"Meta-analysis and imputation refines the association of 15q25 with smoking quantity","year":2010,"lang":"en","type":"review","venue":"Nature Genetics","topic":"Cancer-related molecular mechanisms research","field":"Biochemistry, Genetics and Molecular Biology","cited_by":618,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Toronto; Centre for Addiction and Mental Health; University of Ottawa","funders":"National Institute on Aging; National Institutes of Health; University of Oxford; National Institute on Drug Abuse; GlaxoSmithKline","keywords":"Imputation (statistics); Biology; Locus (genetics); Genome-wide association study; Genetics; 1000 Genomes Project; Genetic association; Single-nucleotide polymorphism; SNP; Meta-analysis; Population; Gene; Genotype; Statistics; Internal medicine; Medicine; Environmental health; Missing data","score_opus":0.03317588789803239,"score_gpt":0.35160367675499327,"score_spread":0.3184277888569609,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2122791877","genre_codex":"review","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":null,"domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.0057121855,0.97766167,0.012034976,0.002431758,0.00043975492,0.000025679303,0.0009358348,0.00013723692,0.00062093796],"genre_scores_gemma":[0.08505655,0.8805882,0.02564744,0.0027472149,0.0017950747,0.00009424617,0.0028087005,0.0001533197,0.0011092667],"study_design_codex":"design_other","study_design_gemma":"meta_analysis","domain_scores_codex":[0.9969818,0.0015750609,0.00027458798,0.0006546782,0.00043648478,0.00007736546],"domain_scores_gemma":[0.9856764,0.011878475,0.0006052966,0.0009922527,0.0007405245,0.00010710133],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.013687515,0.0022263932,0.006711622,0.002099574,0.00024429383,0.001655963,0.003892097,0.0019745212,0.0026060566],"category_scores_gemma":[0.017041963,0.0010086352,0.005342678,0.0040208567,0.0005907155,0.0009835149,0.0011016106,0.0025202336,0.00066871],"study_design_candidate":"meta_analysis","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0018106936,0.00007739597,0.029731832,0.010938752,0.058582492,0.00040659626,0.000085999745,0.0055166697,0.0016243374,0.00276224,0.01411378,0.8743491],"study_design_scores_gemma":[0.0036667967,0.0017966509,0.22431588,0.018983122,0.31286585,0.00992018,0.0003136522,0.022150606,0.0070743132,0.10369228,0.2946516,0.0005690132],"about_ca_topic_score_codex":0.0050956635,"about_ca_topic_score_gemma":0.009373487,"teacher_disagreement_score":0.013687515,"about_ca_system_score_codex":0.0008411102,"about_ca_system_score_gemma":0.0018598187,"threshold_uncertainty_score":0.0723874},"labels":[],"label_agreement":null},{"id":"W2124651100","doi":"10.1038/ng.2202","title":"Complex reorganization and predominant non-homologous repair following chromosomal breakage in karyotypically balanced germline rearrangements and transgenic integration","year":2012,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Genomic variations and chromosomal abnormalities","field":"Biochemistry, Genetics and Molecular Biology","cited_by":260,"is_retracted":false,"has_abstract":false,"route_ca_aff":false,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"","funders":"National Institute of Neurological Disorders and Stroke; National Institute of General Medical Sciences; National Institute of Mental Health; Canadian Institutes of Health Research; Broad Institute; Neurological Foundation of New Zealand; Eunice Kennedy Shriver National Institute of Child Health and Human Development; Autism Speaks; CHDI Foundation; Massachusetts General Hospital","keywords":"Biology; Germline; Chromothripsis; Genetics; Breakpoint; Chromosomal translocation; Chromosomal inversion; Gene rearrangement; Genome; Transgene; Homologous chromosome; Chromosomal rearrangement; DNA; Karyotype; Chromosome; Gene; Genome instability; DNA damage","score_opus":0.005648287601988201,"score_gpt":0.236319402071758,"score_spread":0.2306711144697698,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2124651100","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99733377,0.00031034733,0.0013450278,0.000026788983,0.000006968791,0.000007549841,0.0001736303,0.000056059045,0.00073983945],"genre_scores_gemma":[0.9978405,0.00011163234,0.00043404909,0.000013619174,0.0000035151522,0.000009004214,0.00030657716,0.00004581622,0.001235139],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.99976784,0.000022784809,0.000017864944,0.000057830115,0.000058487978,0.0000751118],"domain_scores_gemma":[0.9996338,0.00006438805,0.00011429813,0.000059852566,0.000024400708,0.00010327521],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0001379078,0.00023115377,0.00020194604,0.00059767306,0.00021234324,0.00045164136,0.00034372113,0.0004284863,0.0026885734],"category_scores_gemma":[0.00028030583,0.00033029975,0.0002584082,0.00024544483,0.00030558542,0.00028993297,0.0005118679,0.00059255265,0.00046552846],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00007815838,0.000009306794,0.0003291369,0.000005529453,0.000004367072,0.000094706214,0.00001082915,0.000030740008,0.99898535,0.00012877182,0.000011069147,0.0003119979],"study_design_scores_gemma":[0.00002531463,0.00013299003,0.036082957,0.00000325744,0.000027516924,0.0012415057,0.000063979496,0.0009723816,0.96038216,0.00018102345,0.000878173,0.000008739004],"about_ca_topic_score_codex":0.0011111933,"about_ca_topic_score_gemma":0.0013691592,"teacher_disagreement_score":0.0026885734,"about_ca_system_score_codex":0.0003297727,"about_ca_system_score_gemma":0.00013628835,"threshold_uncertainty_score":0.008994222},"labels":[],"label_agreement":null},{"id":"W2124756504","doi":"10.1038/ng.2649","title":"DNA hypomethylation within specific transposable element families associates with tissue-specific enhancer landscape","year":2013,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Epigenetics and DNA Methylation","field":"Biochemistry, Genetics and Molecular Biology","cited_by":250,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of British Columbia; Canada's Michael Smith Genome Sciences Centre; BC Cancer Agency","funders":"National Institute of Environmental Health Sciences; National Cancer Institute; National Institute of General Medical Sciences; Howard Hughes Medical Institute; National Institute on Drug Abuse; National Human Genome Research Institute","keywords":"Biology; Enhancer; DNA methylation; Transposable element; Epigenetics; Genetics; Epigenomics; Methylation; Gene; Genome; Epigenetics of physical exercise; Human genome; CpG site; Regulation of gene expression; Transcription factor; Gene expression","score_opus":0.006683541721422851,"score_gpt":0.23102167905979462,"score_spread":0.22433813733837177,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2124756504","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99420375,0.0010442351,0.0035473958,0.000074955366,0.000008440749,0.000004449957,0.0002445975,0.00007091442,0.00080130977],"genre_scores_gemma":[0.9968616,0.00030173283,0.00081788516,0.000040338113,0.0000073186834,0.0000059427207,0.00039942464,0.000020651125,0.0015450775],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9998779,0.000011890142,0.0000057880043,0.00004897236,0.000029819152,0.000025603227],"domain_scores_gemma":[0.9997701,0.00004220111,0.00009283,0.00002507224,0.00002674547,0.00004307049],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00016323326,0.00013432815,0.00019303788,0.00045697557,0.000109948574,0.0003064487,0.00024138395,0.00021751475,0.0015174414],"category_scores_gemma":[0.00026459206,0.00022208874,0.00015413658,0.00023890634,0.00022044026,0.00017937688,0.0002485337,0.00036480126,0.00032553918],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.000058600286,0.000006068612,0.005787004,0.000010873042,0.000012190592,0.00003725987,0.000023973618,0.000036697045,0.9921972,0.00011281409,0.000034864952,0.0016825376],"study_design_scores_gemma":[0.000016672271,0.00016671675,0.5631601,0.0000086036125,0.00006592339,0.0013750317,0.00012744895,0.0017369105,0.43059957,0.0007809912,0.001945394,0.00001655108],"about_ca_topic_score_codex":0.0006994985,"about_ca_topic_score_gemma":0.0017481012,"teacher_disagreement_score":0.0015174414,"about_ca_system_score_codex":0.00018784004,"about_ca_system_score_gemma":0.00011347153,"threshold_uncertainty_score":0.005076349},"labels":[],"label_agreement":null},{"id":"W2126114820","doi":"10.1038/ng1472","title":"A transcriptomic analysis of the phylum Nematoda","year":2004,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Parasite Biology and Host Interactions","field":"Environmental Science","cited_by":269,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Hospital for Sick Children; SickKids Foundation","funders":"National Institutes of Health; National Institute of Allergy and Infectious Diseases; Hospital for Sick Children; Wellcome Trust","keywords":"Phylum; Biology; Nematode; Gene; Caenorhabditis elegans; Evolutionary biology; Phylogenetics; Transcriptome; Genetics; Ecology; Gene expression","score_opus":0.00622039111564887,"score_gpt":0.2941943580347033,"score_spread":0.2879739669190544,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2126114820","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.98124564,0.0028054686,0.0048211776,0.0003176829,0.000051890875,0.00003694967,0.008062159,0.00007606755,0.0025828693],"genre_scores_gemma":[0.9678439,0.0033505298,0.0109218545,0.00030935192,0.00007166324,0.00009578003,0.012856896,0.000074980984,0.0044750525],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9998987,0.000008473441,0.0000047784165,0.00003401017,0.000023792833,0.000030228792],"domain_scores_gemma":[0.9998716,0.00003046851,0.000025778243,0.000010257906,0.000029358147,0.000032599342],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00009799235,0.00026470053,0.00027128158,0.00062127615,0.00052567053,0.0004342561,0.00015041918,0.00028270064,0.0013220777],"category_scores_gemma":[0.0001728975,0.00013081607,0.00028228265,0.00063003926,0.00021588684,0.00025669174,0.00031053706,0.00036948555,0.00037865757],"study_design_candidate":"bench_or_experimental","study_design_consensus":"bench_or_experimental","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00007292298,0.000005731817,0.001324803,0.000031914522,0.000005759664,0.00003887883,0.000016974864,0.000019732392,0.9964521,0.000060432154,0.000060907932,0.0019100137],"study_design_scores_gemma":[0.000037523372,0.0004885919,0.52681,0.00007135797,0.00016209068,0.0013457104,0.00059694215,0.0025812075,0.44982174,0.00077659567,0.017278828,0.00002939289],"about_ca_topic_score_codex":0.0008735204,"about_ca_topic_score_gemma":0.00248872,"teacher_disagreement_score":0.0013220777,"about_ca_system_score_codex":0.00023753878,"about_ca_system_score_gemma":0.00030524822,"threshold_uncertainty_score":0.0044228435},"labels":[],"label_agreement":null},{"id":"W2126824241","doi":"10.1038/ng.2237","title":"Common variants at 12q14 and 12q24 are associated with hippocampal volume","year":2012,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Alzheimer's disease research and treatments","field":"Medicine","cited_by":245,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"WSP (Canada)","funders":"National Human Genome Research Institute; National Center for Research Resources; National Institute of Neurological Disorders and Stroke; National Institute of Mental Health; National Heart, Lung, and Blood Institute; U.S. Public Health Service; National Institute on Aging; National Institutes of Health","keywords":"Biology; Genetics","score_opus":0.016840470687026557,"score_gpt":0.29291354810585435,"score_spread":0.2760730774188278,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2126824241","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99514186,0.001807727,0.0008319737,0.00027667958,0.00005935624,0.000013522397,0.0010055829,0.00010134276,0.0007619054],"genre_scores_gemma":[0.9965994,0.0004923346,0.000998152,0.00006886683,0.00008890053,0.000021786573,0.00062884577,0.00006406111,0.0010377357],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9992669,0.000121085526,0.000096905285,0.00027448338,0.00016265178,0.00007808942],"domain_scores_gemma":[0.9957385,0.0010364635,0.0023476298,0.00027965402,0.00030902078,0.0002886988],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00050793984,0.0017909578,0.001203039,0.0034570042,0.00079497765,0.0010951619,0.0018168594,0.0014646658,0.007350129],"category_scores_gemma":[0.0038424889,0.0009478705,0.0015490332,0.0035652793,0.00074912154,0.0005563786,0.00083008263,0.0011043272,0.0003999473],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.007505528,0.0002854438,0.8311018,0.00041256635,0.007824383,0.0149012655,0.001199233,0.0015517422,0.0985279,0.0009685638,0.0028555503,0.03286603],"study_design_scores_gemma":[0.000092943024,0.00015417015,0.98540825,0.000036873244,0.0010048518,0.008618278,0.00016036753,0.00036170275,0.0022271655,0.0011389242,0.0007530327,0.000043540378],"about_ca_topic_score_codex":0.0070135687,"about_ca_topic_score_gemma":0.00771769,"teacher_disagreement_score":0.007350129,"about_ca_system_score_codex":0.0004467868,"about_ca_system_score_gemma":0.0003360603,"threshold_uncertainty_score":0.024588585},"labels":[],"label_agreement":null},{"id":"W2126864982","doi":"10.1038/ng.669","title":"A locus on 19p13 modifies risk of breast cancer in BRCA1 mutation carriers and is associated with hormone receptor–negative breast cancer in the general population","year":2010,"lang":"en","type":"article","venue":"Nature Genetics","topic":"BRCA gene mutations in cancer","field":"Biochemistry, Genetics and Molecular Biology","cited_by":342,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Centre hospitalier universitaire de Québec; Cancer Care Ontario; Women's College Hospital; University of Toronto; Lunenfeld-Tanenbaum Research Institute; Mount Sinai Hospital","funders":"National Center for Research Resources; National Cancer Institute; National Institutes of Health; Cancer Research UK; Wellcome Trust; Breast Cancer Research Foundation","keywords":"Breast cancer; Single-nucleotide polymorphism; Oncology; Internal medicine; Estrogen receptor; Population; Genome-wide association study; Odds ratio; Biology; Cancer; Case-control study; Genetics; Medicine; Genotype; Gene","score_opus":0.004329126627748607,"score_gpt":0.2591319283407291,"score_spread":0.25480280171298053,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2126864982","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9989236,0.00023487321,0.00016979963,0.000075603006,0.000014978029,0.000004224916,0.00019023061,0.000014119148,0.00037264565],"genre_scores_gemma":[0.9988211,0.00014254918,0.00015156707,0.000032222644,0.000028201477,0.000005355419,0.00015163734,0.000013465205,0.000653951],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9994672,0.00019256762,0.00002950595,0.00016313992,0.000072906776,0.000074703006],"domain_scores_gemma":[0.9986401,0.00047344732,0.00045485632,0.00009659527,0.00007109913,0.0002638591],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00036673568,0.00091115496,0.0006524222,0.0022149782,0.00063065835,0.00047567065,0.0007242713,0.0009310969,0.0050740708],"category_scores_gemma":[0.0018071798,0.0005649608,0.0007405921,0.0015763247,0.0005442288,0.00031492068,0.00041036805,0.0006407385,0.00041684223],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0036996985,0.00027978694,0.9467577,0.00004301545,0.0007226915,0.005146496,0.0004478288,0.00026283626,0.033538926,0.00020977188,0.00044922304,0.008442101],"study_design_scores_gemma":[0.00004346968,0.00024908452,0.9943045,0.000008667048,0.00019718285,0.0035823812,0.00010325048,0.0002619598,0.0008885287,0.0001380347,0.00021184006,0.000011059251],"about_ca_topic_score_codex":0.0051531144,"about_ca_topic_score_gemma":0.0022138834,"teacher_disagreement_score":0.0051531144,"about_ca_system_score_codex":0.00020849667,"about_ca_system_score_gemma":0.00021093112,"threshold_uncertainty_score":0.016974509},"labels":[],"label_agreement":null},{"id":"W2127442418","doi":"10.1038/ng.209","title":"Collaborative genome-wide association analysis supports a role for ANK3 and CACNA1C in bipolar disorder","year":2008,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Genetic Associations and Epidemiology","field":"Biochemistry, Genetics and Molecular Biology","cited_by":1258,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of British Columbia Hospital","funders":"National Center for Research Resources; National Institute of Mental Health; Medical Research Council; Sylvan C. Herman Foundation; Broad Institute; Wellcome Trust; Science Foundation Ireland; National Alliance for Research on Schizophrenia and Depression","keywords":"Bipolar disorder; Genome-wide association study; Ankyrin; Biology; Genetic association; Genetics; Calcium channel; Protein subunit; Bipolar II disorder; G alpha subunit; Gene; Single-nucleotide polymorphism; Neuroscience; Internal medicine; Genotype; Medicine; Calcium; Cognition","score_opus":0.003454939108839631,"score_gpt":0.24417356233945797,"score_spread":0.24071862323061835,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2127442418","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.990642,0.0022892216,0.0028313561,0.0009483073,0.000084601896,0.000020573229,0.0010375528,0.000063330735,0.0020831875],"genre_scores_gemma":[0.9977164,0.00040243374,0.0011203181,0.00011272833,0.00004272593,0.000008905031,0.00026574905,0.000013680808,0.00031711528],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9983132,0.0006055297,0.00017465085,0.00054203905,0.00023372113,0.00013076753],"domain_scores_gemma":[0.99459153,0.0024113453,0.0013750646,0.00061377254,0.000599107,0.000409138],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0025380503,0.0005654635,0.0006892994,0.0017835813,0.0012449198,0.0009827,0.0009099563,0.0012638639,0.0047258767],"category_scores_gemma":[0.007496181,0.00034117076,0.001152729,0.0022207892,0.0006966561,0.0004291097,0.0007012569,0.0011601312,0.00030259122],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0034526642,0.00009887776,0.9542414,0.0001696838,0.003182379,0.0019580505,0.0004438859,0.0004432239,0.02046804,0.00081820355,0.0014170598,0.013306524],"study_design_scores_gemma":[0.00020085362,0.00020236273,0.98808074,0.00005466496,0.0022228104,0.0030018704,0.00025491527,0.0013705854,0.0021333222,0.0011898577,0.0012549211,0.000033064753],"about_ca_topic_score_codex":0.014354885,"about_ca_topic_score_gemma":0.011299138,"teacher_disagreement_score":0.014354885,"about_ca_system_score_codex":0.00042493828,"about_ca_system_score_gemma":0.0005667479,"threshold_uncertainty_score":0.028542638},"labels":[],"label_agreement":null},{"id":"W2127861463","doi":"10.1038/ng.132","title":"TARDBP mutations in individuals with sporadic and familial amyotrophic lateral sclerosis","year":2008,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Amyotrophic Lateral Sclerosis Research","field":"Medicine","cited_by":1526,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Université Laval; Hôpital de l'Enfant-Jésus; University of Waterloo; Université de Montréal; Centre Hospitalier de l’Université de Montréal","funders":"","keywords":"Amyotrophic lateral sclerosis; TARDBP; Biology; Missense mutation; Pathogenesis; Genetics; Mutation; SOD1; Pathology; Disease; Gene; Medicine; Immunology","score_opus":0.025812371288376934,"score_gpt":0.275998133620191,"score_spread":0.25018576233181405,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2127861463","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9991025,0.00017427362,0.00005430507,0.000048227896,0.000014177339,0.0000048544557,0.00010989046,0.000008364017,0.00048343965],"genre_scores_gemma":[0.99946076,0.000051214658,0.00006442715,0.00003462995,0.000021573662,0.000004977848,0.000102140526,0.000005818368,0.00025448983],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99937576,0.000107680105,0.0001326723,0.00017003436,0.00010978422,0.00010396501],"domain_scores_gemma":[0.9989208,0.00043605224,0.00027061984,0.000049896586,0.000120100696,0.00020244537],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00053889013,0.0011933361,0.0008996988,0.0028383916,0.0016511314,0.00075827504,0.0006628181,0.0019752448,0.0034977684],"category_scores_gemma":[0.003788568,0.00060737535,0.0006449761,0.0014408873,0.0008522259,0.0007223819,0.00070629653,0.00063285424,0.0004610454],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0057979524,0.00024635883,0.93421084,0.00007638378,0.00034935863,0.038170215,0.0017222228,0.00036760257,0.01129155,0.0002656161,0.0006187842,0.0068831346],"study_design_scores_gemma":[0.00015524853,0.00049063575,0.95777124,0.000032700333,0.00028780097,0.03810002,0.001056474,0.00061851495,0.00063436496,0.00043388878,0.00037725232,0.000041950636],"about_ca_topic_score_codex":0.0066073136,"about_ca_topic_score_gemma":0.0046848585,"teacher_disagreement_score":0.0066073136,"about_ca_system_score_codex":0.00050050975,"about_ca_system_score_gemma":0.00030339716,"threshold_uncertainty_score":0.013137758},"labels":[],"label_agreement":null},{"id":"W2128700722","doi":"10.1038/ng1947","title":"Biallelic mutations in PALB2 cause Fanconi anemia subtype FA-N and predispose to childhood cancer","year":2006,"lang":"en","type":"article","venue":"Nature Genetics","topic":"BRCA gene mutations in cancer","field":"Biochemistry, Genetics and Molecular Biology","cited_by":643,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"McGill University; Jewish General Hospital","funders":"National Cancer Institute; National Heart, Lung, and Blood Institute; Wellcome Trust","keywords":"Fanconi anemia; PALB2; Biology; BRCA2 Protein; Genetics; Mutation; Cancer; Cancer research; DNA repair; Germline mutation; Gene","score_opus":0.00563040447115641,"score_gpt":0.27212228751987966,"score_spread":0.26649188304872323,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2128700722","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.991169,0.0009196053,0.0012778552,0.00036045213,0.000047541107,0.000036054134,0.00062518433,0.000104442675,0.005459865],"genre_scores_gemma":[0.99710435,0.0002951143,0.00077884353,0.000058249494,0.000028022156,0.000013733037,0.00021078721,0.000037991103,0.0014728103],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9997465,0.00005287969,0.000019472265,0.00006137399,0.000077807614,0.000042034186],"domain_scores_gemma":[0.99944276,0.00018006323,0.00019420372,0.000031649204,0.000024406494,0.00012693775],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00020540469,0.0008309987,0.0003366627,0.0020438938,0.0007807267,0.00035251575,0.00047406775,0.00094985537,0.008444828],"category_scores_gemma":[0.00072431273,0.00043191097,0.00024041836,0.0011208775,0.0005391008,0.00025367778,0.0005435992,0.00060937816,0.00072800944],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0022775107,0.0004908006,0.33510736,0.0002844884,0.00031854567,0.15670371,0.0015149661,0.001107176,0.45716098,0.004692504,0.004811124,0.03553085],"study_design_scores_gemma":[0.00014411485,0.00029328297,0.63157517,0.000088385874,0.0002365656,0.29888564,0.0008229318,0.0014356751,0.051580817,0.001586291,0.013297989,0.000053096734],"about_ca_topic_score_codex":0.00208113,"about_ca_topic_score_gemma":0.0026108029,"teacher_disagreement_score":0.008444828,"about_ca_system_score_codex":0.00034212443,"about_ca_system_score_gemma":0.00028583605,"threshold_uncertainty_score":0.028250694},"labels":[],"label_agreement":null},{"id":"W2130462669","doi":"10.1038/ng.2616","title":"Dense genotyping of immune-related disease regions identifies nine new risk loci for primary sclerosing cholangitis","year":2013,"lang":"en","type":"review","venue":"Nature Genetics","topic":"Liver Diseases and Immunity","field":"Medicine","cited_by":398,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Montreal Heart Institute; Mount Sinai Hospital; Hospital for Sick Children; University of Toronto; Université de Montréal; University of Alberta; University of Calgary","funders":"National Center for Advancing Translational Sciences; Lerner Research Institute, Cleveland Clinic; University of California, Davis; Université de Paris; Institut de Cardiologie de Montréal; Universitätsklinikum Hamburg-Eppendorf; Akershus Universitetssykehus; University of Thessaly; Assistance publique-Hôpitaux de Paris; Graduate School of Public Health, University of Pittsburgh; Terveyden ja hyvinvoinnin laitos; Rheinische Friedrich-Wilhelms-Universität Bonn; Hospital for Sick Children; University of California, San Diego; Yale University; University of Toronto; Medizinischen Hochschule Hannover; Pomorski Uniwersytet Medyczny W Szczecinie; Université de Montréal; Helmholtz Zentrum München; Sapienza Università di Roma; Universität zu Lübeck; Karolinska Institutet; Cleveland Clinic; Rijksuniversiteit Groningen; Queen Mary University of London; National Institute for Health and Care Research; Deutsche Forschungsgemeinschaft; Helsingin Yliopisto; University of Alberta; Universitat de Barcelona; National Cancer Institute; Landspítali Háskólasjúkrahús; Department of Medicine, University of Toronto; Sahlgrenska Akademin; University of Pittsburgh; Technische Universität München; Universitetet i Oslo; KU Leuven; Università degli Studi di Padova; National Institute of Diabetes and Digestive and Kidney Diseases; Barts and The London School of Medicine and Dentistry; Norges Teknisk-Naturvitenskapelige Universitet; Wellcome Trust","keywords":"Biology; Primary sclerosing cholangitis; Genotyping; Immune system; Disease; Genetics; Primary (astronomy); Immunology; Genotype; Gene; Internal medicine","score_opus":0.03243024631360305,"score_gpt":0.3112429783503695,"score_spread":0.2788127320367665,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2130462669","genre_codex":"review","genre_gemma":"review","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"review","genre_consensus":"review","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.0012306359,0.9949614,0.0013042795,0.0010035206,0.00024940906,0.000006562136,0.00006327121,0.000024121959,0.0011568491],"genre_scores_gemma":[0.009064607,0.98562014,0.002036564,0.0012331276,0.0008040994,0.000016921927,0.00017942481,0.0000057185553,0.0010394022],"study_design_codex":"design_other","study_design_gemma":"observational","domain_scores_codex":[0.9997013,0.000057205463,0.000034861114,0.00007849394,0.00010405602,0.000023951492],"domain_scores_gemma":[0.99926656,0.0004608138,0.00009825421,0.000022701308,0.000107250526,0.000044454973],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0008136886,0.00079323,0.0010649211,0.00089989,0.00010130686,0.00058709993,0.0009055522,0.0010382032,0.0011589692],"category_scores_gemma":[0.0011697598,0.00024870722,0.00040770933,0.0009264687,0.00045053646,0.0004466999,0.00042969215,0.001132343,0.00061744335],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00012025049,0.000038108145,0.003006691,0.0023947656,0.00019170727,0.000349653,0.000023174634,0.0002473517,0.0024296516,0.0013866912,0.012894255,0.97691774],"study_design_scores_gemma":[0.00026642773,0.0003187634,0.0379368,0.004843249,0.0015606424,0.0084257815,0.00015267271,0.00069621997,0.0033268724,0.011292557,0.9310659,0.00011417179],"about_ca_topic_score_codex":0.0010835801,"about_ca_topic_score_gemma":0.0019556745,"teacher_disagreement_score":0.0011589692,"about_ca_system_score_codex":0.0003531314,"about_ca_system_score_gemma":0.00065193546,"threshold_uncertainty_score":0.0043032765},"labels":[],"label_agreement":null},{"id":"W2130979463","doi":"10.1038/ng.479","title":"Genetic variants at CD28, PRDM1 and CD2/CD58 are associated with rheumatoid arthritis risk","year":2009,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Chronic Lymphocytic Leukemia Research","field":"Medicine","cited_by":355,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University Health Network; Mount Sinai Hospital; University of Toronto","funders":"National Center for Research Resources; National Institute of Arthritis and Musculoskeletal and Skin Diseases; National Institute of Allergy and Infectious Diseases; National Human Genome Research Institute; National Institute for Health and Care Research; Canadian Institutes of Health Research; National Institutes of Health; National Institute of Diabetes and Digestive and Kidney Diseases; Versus Arthritis; National Heart, Lung, and Blood Institute","keywords":"Single-nucleotide polymorphism; Genome-wide association study; Biology; Genetics; Rheumatoid arthritis; Genetic association; Replication (statistics); Arthritis; Gene; Bioinformatics; Genotype; Immunology; Virology","score_opus":0.007128330863492305,"score_gpt":0.25385256817739704,"score_spread":0.24672423731390475,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2130979463","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9980305,0.00047212024,0.0003409192,0.000121507255,0.000025199119,0.0000057967586,0.00009987224,0.000018742492,0.000885293],"genre_scores_gemma":[0.9991066,0.000087678534,0.00029841778,0.00003088338,0.000034117045,0.0000044138296,0.000063270396,0.0000075171324,0.00036712122],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9993773,0.00025243513,0.00006315905,0.00013534886,0.00010108528,0.000070808346],"domain_scores_gemma":[0.997872,0.00093583367,0.0006222972,0.0001435645,0.000114131726,0.00031229042],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.000481917,0.0007915704,0.0005301774,0.0011868875,0.0005095245,0.0004863648,0.00061172876,0.0010611847,0.0043685064],"category_scores_gemma":[0.002986598,0.00037338195,0.0005334182,0.0009667902,0.0004052607,0.00022912845,0.00027451932,0.00088787894,0.00044458482],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0049552824,0.0003122981,0.91636425,0.00009281638,0.0008195107,0.007330504,0.00033893998,0.0005586182,0.058259927,0.00048814103,0.00061402435,0.00986572],"study_design_scores_gemma":[0.00023491726,0.0005109652,0.9804894,0.000027977083,0.000589395,0.011498615,0.00018609573,0.0018363916,0.0031735087,0.0007371124,0.0006859533,0.000029763023],"about_ca_topic_score_codex":0.0015314127,"about_ca_topic_score_gemma":0.0010242186,"teacher_disagreement_score":0.0043685064,"about_ca_system_score_codex":0.00018642386,"about_ca_system_score_gemma":0.00016812932,"threshold_uncertainty_score":0.014614105},"labels":[],"label_agreement":null},{"id":"W2131328125","doi":"10.1038/ng.838","title":"Genome-wide association and linkage identify modifier loci of lung disease severity in cystic fibrosis at 11p13 and 20q13.2","year":2011,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Cystic Fibrosis Research Advances","field":"Medicine","cited_by":232,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Centre Hospitalier de l’Université de Montréal; Institute for Clinical Evaluative Sciences; University of Toronto; SickKids Foundation; University of British Columbia; Hospital for Sick Children; Public Health Ontario","funders":"National Human Genome Research Institute; National Institute of Mental Health; National Institute of Diabetes and Digestive and Kidney Diseases; National Heart, Lung, and Blood Institute; Canadian Institutes of Health Research","keywords":"Genome-wide association study; Biology; Quantitative trait locus; Cystic fibrosis; Locus (genetics); Genetics; Genetic association; Odds ratio; Genetic linkage; Internal medicine; Genotype; Medicine; Single-nucleotide polymorphism; Gene","score_opus":0.01132290252284309,"score_gpt":0.28682744760900264,"score_spread":0.27550454508615957,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2131328125","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.995618,0.00080819585,0.0015923057,0.00036310815,0.000031665946,0.000017382214,0.0006003659,0.00003705798,0.0009319886],"genre_scores_gemma":[0.9966126,0.00028634947,0.0016364944,0.000067486406,0.000035978817,0.000024478975,0.00046299907,0.000018237506,0.00085533864],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9991689,0.00022654052,0.00006458173,0.00018636903,0.00020882336,0.00014489098],"domain_scores_gemma":[0.99828595,0.0007795286,0.00047546744,0.00010123097,0.00012980375,0.00022806249],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0010162629,0.000632831,0.00047315852,0.0016909327,0.0004964553,0.00068031764,0.0006206876,0.00087074726,0.0045447717],"category_scores_gemma":[0.002953204,0.00030443302,0.0007177288,0.0015294651,0.0005529032,0.00021331098,0.00085641135,0.00087652105,0.00030970626],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.005611476,0.000258072,0.8304741,0.00013630236,0.0012342646,0.004461405,0.0006050916,0.0018010153,0.11114984,0.001929944,0.0023312464,0.040007208],"study_design_scores_gemma":[0.00017981141,0.00012764541,0.9880425,0.00002674902,0.00040998604,0.0024785323,0.00012521785,0.0012114011,0.0052307625,0.00082008075,0.0013267361,0.000020719499],"about_ca_topic_score_codex":0.0053114295,"about_ca_topic_score_gemma":0.008085144,"teacher_disagreement_score":0.0053114295,"about_ca_system_score_codex":0.00036807416,"about_ca_system_score_gemma":0.00038756957,"threshold_uncertainty_score":0.015203774},"labels":[],"label_agreement":null},{"id":"W2132322753","doi":"10.1038/ng.2453","title":"Loss-of-function mutations in IGSF1 cause an X-linked syndrome of central hypothyroidism and testicular enlargement","year":2012,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Growth Hormone and Insulin-like Growth Factors","field":"Medicine","cited_by":215,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Health Canada; McGill University","funders":"National Institute of Diabetes and Digestive and Kidney Diseases; NIHR Cambridge Biomedical Research Centre; National Health and Medical Research Council; Medical Research Council; National Institutes of Health; Natural Sciences and Engineering Research Council of Canada; Leids Universitair Medisch Centrum; Istituto Auxologico Italiano; Ministero della Salute; China Scholarship Council; National Institute for Health and Care Research; Wellcome Trust; McGill University; University of Chicago","keywords":"Endocrinology; Internal medicine; Biology; Anterior pituitary; Thyroid; Prolactin; Pituitary gland; Central hypothyroidism; Exome sequencing; Thyrotropin-releasing hormone; Hormone; Mutation; Gene; Genetics; Medicine","score_opus":0.0175053296548005,"score_gpt":0.2678451694446227,"score_spread":0.2503398397898222,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2132322753","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9956311,0.0005443402,0.0012655625,0.00038441352,0.00006583442,0.000016451622,0.0002399785,0.00013567555,0.0017165635],"genre_scores_gemma":[0.9987754,0.000092101036,0.00044859864,0.000049540424,0.00003408554,0.0000035814378,0.00005459205,0.000015384054,0.00052674214],"study_design_codex":"case_report","study_design_gemma":"observational","domain_scores_codex":[0.9998055,0.00003200755,0.000018149885,0.000040630537,0.00006778615,0.0000359771],"domain_scores_gemma":[0.99938893,0.0002670853,0.00013795338,0.000024092136,0.00002282819,0.00015909274],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00021483857,0.0014497981,0.00041078805,0.0009985542,0.0005187164,0.00034017194,0.0006259567,0.0011594291,0.0021869286],"category_scores_gemma":[0.0006693138,0.00026533095,0.0005050701,0.00055534334,0.001110497,0.00017482416,0.0004283344,0.0007044496,0.00024959302],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.001902164,0.00019648683,0.053857412,0.00017761825,0.0003262628,0.49140835,0.0008753672,0.0018255917,0.42873037,0.0021226103,0.0019471406,0.016630625],"study_design_scores_gemma":[0.0005473319,0.0010385083,0.29026452,0.00007640063,0.00049108296,0.5770204,0.00065285614,0.0059996354,0.11727695,0.0013778765,0.005152791,0.0001017075],"about_ca_topic_score_codex":0.00210556,"about_ca_topic_score_gemma":0.00219849,"teacher_disagreement_score":0.0021869286,"about_ca_system_score_codex":0.00047085693,"about_ca_system_score_gemma":0.00033843226,"threshold_uncertainty_score":0.0073159933},"labels":[],"label_agreement":null},{"id":"W2132323730","doi":"10.1038/ng.528","title":"Plasmodium falciparum genome-wide scans for positive selection, recombination hot spots and resistance to antimalarial drugs","year":2010,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Malaria Research and Control","field":"Medicine","cited_by":198,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Calgary; Université de Montréal; Centre Hospitalier Universitaire Sainte-Justine","funders":"National Institutes of Health; Wellcome Trust","keywords":"Biology; Plasmodium falciparum; Genome-wide association study; Genotyping; Genome; Genetics; Malaria; Population; Drug resistance; SNP array; Gene; Virology; Genotype; Single-nucleotide polymorphism; Immunology","score_opus":0.005578621909910725,"score_gpt":0.26824420132947024,"score_spread":0.26266557941955954,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2132323730","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.998606,0.00030783462,0.00019258473,0.00008244539,0.0000036505576,0.0000037285843,0.00046945937,0.000017144996,0.00031707977],"genre_scores_gemma":[0.999012,0.00009676191,0.00027169375,0.000044480028,0.000008331965,0.0000047215613,0.00036325102,0.0000073441097,0.00019132256],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9996996,0.00007143801,0.000015892465,0.00011150879,0.00004703611,0.000054510623],"domain_scores_gemma":[0.9991603,0.0004347861,0.00021548252,0.000042878448,0.00003415198,0.00011243301],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0005320193,0.00020156208,0.000455829,0.0008919673,0.0003990552,0.0003508469,0.0003401257,0.00042159137,0.002565257],"category_scores_gemma":[0.00095527124,0.00024717182,0.00040792022,0.0011012307,0.0003155103,0.0001609092,0.00033292026,0.0005516707,0.00013069052],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0060068774,0.00017281107,0.6406634,0.00036380463,0.002598091,0.0015037443,0.0005727305,0.0013889361,0.30846858,0.00063910015,0.0031586394,0.03446331],"study_design_scores_gemma":[0.000058858215,0.0001295047,0.99581003,0.000004083299,0.00027634753,0.00072186394,0.00011125792,0.00049182103,0.0017110521,0.000114362825,0.0005624365,0.000008515286],"about_ca_topic_score_codex":0.0020978414,"about_ca_topic_score_gemma":0.0058331047,"teacher_disagreement_score":0.002565257,"about_ca_system_score_codex":0.00014754864,"about_ca_system_score_gemma":0.00014999679,"threshold_uncertainty_score":0.008581638},"labels":[],"label_agreement":null},{"id":"W2132546867","doi":"10.1038/ng.2529","title":"The genetic landscape of high-risk neuroblastoma","year":2013,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Neuroblastoma Research and Treatments","field":"Medicine","cited_by":1219,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of British Columbia; BC Cancer Agency","funders":"National Cancer Institute; National Human Genome Research Institute; National Institute on Minority Health and Health Disparities; Canadian Institutes of Health Research; National Institutes of Health","keywords":"ATRX; Biology; Neuroblastoma RAS viral oncogene homolog; PTPN11; Neuroblastoma; Germline mutation; Germline; Exome sequencing; CHEK2; Genetics; Somatic cell; Cancer research; Mutation; Exome; Gene; KRAS","score_opus":0.0052995840760404565,"score_gpt":0.24927819743861054,"score_spread":0.2439786133625701,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2132546867","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9871071,0.003664813,0.00050871406,0.0026024517,0.00003054405,0.000008902688,0.00038809475,0.00001881386,0.005670501],"genre_scores_gemma":[0.9976615,0.001354927,0.0002749702,0.00012297639,0.00004307994,0.0000029364676,0.00015215072,0.000009833462,0.00037773373],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9995204,0.00014758053,0.000032657426,0.000097623415,0.000121994824,0.00007977036],"domain_scores_gemma":[0.9993912,0.00022608369,0.00017794302,0.000031505886,0.00006878533,0.00010446644],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00028819373,0.00023095087,0.00027718188,0.0010129638,0.00049732847,0.00070233643,0.00044306938,0.00064590375,0.0032422799],"category_scores_gemma":[0.0021713544,0.00015945773,0.00018612758,0.001103213,0.00043382973,0.0004484081,0.0005535993,0.0005451415,0.00025532828],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00078247185,0.00009545189,0.8957937,0.00010479351,0.00025437673,0.010461313,0.0007791095,0.0014520106,0.030506443,0.007062417,0.0025088612,0.050199054],"study_design_scores_gemma":[0.00003413516,0.00017533069,0.94412243,0.00014874674,0.0003466511,0.02608582,0.001678085,0.0016509788,0.004285083,0.014870669,0.0065540886,0.000047942434],"about_ca_topic_score_codex":0.003782628,"about_ca_topic_score_gemma":0.003994302,"teacher_disagreement_score":0.003782628,"about_ca_system_score_codex":0.000432258,"about_ca_system_score_gemma":0.00045907436,"threshold_uncertainty_score":0.010846496},"labels":[],"label_agreement":null},{"id":"W2132559433","doi":"10.1038/ng.2561","title":"Genome-wide association studies identify four ER negative–specific breast cancer risk loci","year":2013,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Genetic Associations and Epidemiology","field":"Biochemistry, Genetics and Molecular Biology","cited_by":421,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"McGill University and Génome Québec Innovation Centre; St. Michael's Hospital; Public Health Ontario; Royal Victoria Hospital; Centre hospitalier universitaire de Québec; McGill University Health Centre; McGill University; Université Laval; Université de Montréal; Royal Victoria Regional Health Centre; Lunenfeld-Tanenbaum Research Institute; Mount Sinai Hospital; University of Toronto","funders":"Canadian Institutes of Health Research; National Cancer Institute; National Institute for Health and Care Research; Cancer Research UK; Wellcome Trust","keywords":"Biology; Genome-wide association study; Breast cancer; Genetics; Genetic association; Computational biology; Single-nucleotide polymorphism; Gene; Cancer; Genotype","score_opus":0.013338927219631324,"score_gpt":0.28822973001306373,"score_spread":0.2748908027934324,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2132559433","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9947989,0.0011792731,0.001973781,0.00029972554,0.00002300967,0.000011814828,0.00039295046,0.000042936343,0.0012776563],"genre_scores_gemma":[0.9977915,0.00028277186,0.001001708,0.000068042544,0.000016423672,0.000007676199,0.00023748458,0.000012771679,0.0005816517],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99938214,0.00016700912,0.00006451128,0.00018285005,0.0001107262,0.00009279655],"domain_scores_gemma":[0.9979213,0.00097201375,0.00061908015,0.0001877,0.0001429993,0.00015699261],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0010218959,0.0006323996,0.00046271758,0.001433019,0.00040709102,0.0007115221,0.0008128668,0.0008567317,0.0032208455],"category_scores_gemma":[0.0022140099,0.00034399307,0.0009385161,0.00152462,0.0005911016,0.00027098405,0.00073979155,0.000665741,0.00038426736],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.002941885,0.0001722359,0.9144652,0.000114476345,0.0013102548,0.001355157,0.0002959763,0.000393248,0.060358204,0.0007077276,0.00044530013,0.01744029],"study_design_scores_gemma":[0.00012955234,0.00021916306,0.986902,0.00002442539,0.0010454628,0.0019277919,0.00018893542,0.0005352386,0.0065726666,0.00096762006,0.0014670762,0.000019995437],"about_ca_topic_score_codex":0.0016515047,"about_ca_topic_score_gemma":0.0018439955,"teacher_disagreement_score":0.0032208455,"about_ca_system_score_codex":0.00023688833,"about_ca_system_score_gemma":0.0002598022,"threshold_uncertainty_score":0.010774851},"labels":[],"label_agreement":null},{"id":"W2133617345","doi":"10.1038/ng1681","title":"Deficiency of UBR1, a ubiquitin ligase of the N-end rule pathway, causes pancreatic dysfunction, malformations and mental retardation (Johanson-Blizzard syndrome)","year":2005,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Ubiquitin and proteasome pathways","field":"Biochemistry, Genetics and Molecular Biology","cited_by":272,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Hospital for Sick Children","funders":"Deutsche Forschungsgemeinschaft; Deutsche Krebshilfe; Ellison Medical Foundation","keywords":"Biology; Ubiquitin ligase; Endocrinology; Exocrine pancreatic insufficiency; Internal medicine; Genetics; Aplasia; Pancreas; Ubiquitin; Gene; Medicine; Anatomy","score_opus":0.007136241350316382,"score_gpt":0.22628922661574372,"score_spread":0.21915298526542734,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2133617345","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.98535514,0.0028377208,0.0056086415,0.0004094584,0.00007319192,0.000028705945,0.0011283562,0.0006257628,0.003933041],"genre_scores_gemma":[0.99067533,0.0011441145,0.003557534,0.000049293583,0.000022939172,0.000013065811,0.00062362483,0.00006947016,0.0038446437],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9997485,0.00003403627,0.000029184983,0.00006839592,0.00008029879,0.00003954177],"domain_scores_gemma":[0.9996499,0.000052626216,0.00013839532,0.00002550394,0.000020569118,0.00011303256],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00020996456,0.0015220222,0.0005639677,0.0014379313,0.00044599513,0.0004609964,0.00039420265,0.00073984923,0.0016251488],"category_scores_gemma":[0.0003867727,0.00040558362,0.00033512418,0.00053151423,0.0006734212,0.00025572296,0.0005544141,0.00068805774,0.0009751298],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0006055525,0.000102372804,0.0042490317,0.00013736227,0.00007754154,0.008036046,0.00006676306,0.0004277512,0.9737603,0.0007812285,0.0008837481,0.01087235],"study_design_scores_gemma":[0.00011296157,0.0003380653,0.040133465,0.000027882994,0.00022193773,0.04707947,0.00008930322,0.0020745876,0.90133697,0.0005479257,0.007994522,0.000042896972],"about_ca_topic_score_codex":0.0021520355,"about_ca_topic_score_gemma":0.0024313813,"teacher_disagreement_score":0.0021520355,"about_ca_system_score_codex":0.0005364878,"about_ca_system_score_gemma":0.00045727647,"threshold_uncertainty_score":0.005436659},"labels":[],"label_agreement":null},{"id":"W2133809942","doi":"10.1038/ng.846","title":"An integrated approach to characterize genetic interaction networks in yeast metabolism","year":2011,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Microbial Metabolic Engineering and Bioproduction","field":"Biochemistry, Genetics and Molecular Biology","cited_by":219,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Toronto","funders":"National Human Genome Research Institute; Biotechnology and Biological Sciences Research Council; Canadian Institutes of Health Research; Wellcome Trust","keywords":"Biology; Pleiotropy; Saccharomyces cerevisiae; Modularity (biology); Computational biology; Gene interaction; Metabolic network; Gene; Systems biology; Genetics; Phenotype","score_opus":0.009944112889242341,"score_gpt":0.22323550379605622,"score_spread":0.21329139090681387,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2133809942","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.6259775,0.0010616876,0.36727497,0.00011462608,0.000021697953,0.00017730976,0.0018369352,0.0008579277,0.0026772926],"genre_scores_gemma":[0.779838,0.0010067743,0.21548574,0.0000685611,0.000014125788,0.00027453725,0.002171638,0.000105521205,0.0010350507],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9998412,0.000030376224,0.000010933345,0.00004388881,0.000053752257,0.000019816507],"domain_scores_gemma":[0.9997806,0.00008166509,0.000041296356,0.00004385832,0.000024806079,0.000027834052],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00020547718,0.00045820154,0.0005154494,0.0011580515,0.00035357405,0.0007731819,0.0003327746,0.0002627073,0.0006603962],"category_scores_gemma":[0.00037353078,0.00025517255,0.00063849095,0.0011665318,0.00028782577,0.0006454462,0.00063755846,0.0006580176,0.0001742771],"study_design_candidate":"bench_or_experimental","study_design_consensus":"bench_or_experimental","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00019849036,0.00009933045,0.0021682382,0.000100226054,0.00010222311,0.00007047293,0.000042159034,0.012390591,0.96023333,0.0055374634,0.0000898813,0.018967656],"study_design_scores_gemma":[0.00006978968,0.0004245392,0.02500848,0.000022109201,0.00031810725,0.00050179777,0.00012269305,0.48079428,0.46741292,0.020702533,0.0045713536,0.00005144575],"about_ca_topic_score_codex":0.0014099705,"about_ca_topic_score_gemma":0.0024636856,"teacher_disagreement_score":0.0014099705,"about_ca_system_score_codex":0.0004968546,"about_ca_system_score_gemma":0.00036762073,"threshold_uncertainty_score":0.003604889},"labels":[],"label_agreement":null},{"id":"W2133821573","doi":"10.1038/ng1453","title":"Loss-of-function mutations in LEMD3 result in osteopoikilosis, Buschke-Ollendorff syndrome and melorheostosis","year":2004,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Dermatological and Skeletal Disorders","field":"Biochemistry, Genetics and Molecular Biology","cited_by":463,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Université de Montréal","funders":"Vlaamse regering; European Commission","keywords":"Biology; Phenotype; Mutation; Genetics; Xenopus; Loss function; Somatic cell; Allele; Gene","score_opus":0.005429291433192692,"score_gpt":0.2369178393610363,"score_spread":0.23148854792784362,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2133821573","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9902838,0.00080898125,0.0029641676,0.00036082105,0.00008247816,0.000034821813,0.0013249646,0.0002930953,0.0038467892],"genre_scores_gemma":[0.99597234,0.00016275219,0.0016005767,0.00010271027,0.00001887061,0.000023721632,0.00052599167,0.000091393274,0.0015016645],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.99967456,0.000056630357,0.00005723067,0.00005089415,0.00011980452,0.00004096314],"domain_scores_gemma":[0.9992951,0.0002734909,0.00018092028,0.000040913434,0.000029676497,0.00017987618],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0002669343,0.001359718,0.0004528064,0.0012525079,0.00052031066,0.0004020797,0.0006561458,0.0014937922,0.003938876],"category_scores_gemma":[0.00091127475,0.0003600339,0.00053049234,0.0005426125,0.0011823925,0.0003036906,0.0007645681,0.00073623774,0.0013151015],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0012048411,0.00015411532,0.010448043,0.00017188102,0.00015951856,0.079057135,0.0002551622,0.0010692962,0.8960941,0.0016129345,0.0013179128,0.008455131],"study_design_scores_gemma":[0.00057483267,0.00037170856,0.13551486,0.0000851588,0.00040358913,0.32296935,0.0007751387,0.0067398385,0.5167203,0.0023229336,0.013376781,0.00014552256],"about_ca_topic_score_codex":0.00086971576,"about_ca_topic_score_gemma":0.001801654,"teacher_disagreement_score":0.003938876,"about_ca_system_score_codex":0.000526518,"about_ca_system_score_gemma":0.00028301508,"threshold_uncertainty_score":0.013176858},"labels":[],"label_agreement":null},{"id":"W2133857310","doi":"10.1038/ng.2566","title":"Multiple independent variants at the TERT locus are associated with telomere length and risks of breast and ovarian cancer","year":2013,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Telomeres, Telomerase, and Senescence","field":"Medicine","cited_by":540,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Université de Montréal; University Health Network; Mount Sinai Hospital; Lunenfeld-Tanenbaum Research Institute; University of Calgary; BC Cancer Agency; Alberta Health Services; Université Laval; McGill University; Simon Fraser University; Women's College Hospital; Royal Victoria Hospital; Centre hospitalier universitaire de Québec; University of Toronto; Public Health Ontario; McGill University and Génome Québec Innovation Centre","funders":"National Institute for Health and Care Research; Canadian Institutes of Health Research; European Commission; National Cancer Institute; Cancer Research UK; Wellcome Trust","keywords":"Biology; Telomere; Locus (genetics); Breast cancer; Genetics; Ovarian cancer; Cancer; Gene","score_opus":0.01670579724287001,"score_gpt":0.265651848862316,"score_spread":0.248946051619446,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2133857310","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9976845,0.001013657,0.0005522529,0.00010374136,0.000021925704,0.0000030908864,0.00020316687,0.000015774733,0.0004018358],"genre_scores_gemma":[0.9990294,0.00020464213,0.00025390158,0.00002561812,0.000031650903,0.0000033269894,0.000120360055,0.000008784958,0.00032221206],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99951434,0.00012999077,0.000051032952,0.00016611998,0.00008221419,0.000056346074],"domain_scores_gemma":[0.9976745,0.00086182787,0.0009197596,0.00020597376,0.00009462001,0.00024326502],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0004892579,0.00054518675,0.00040019024,0.0009065838,0.00036075577,0.0005280511,0.00045841187,0.0009304384,0.0025241924],"category_scores_gemma":[0.0020467658,0.0003478203,0.0009771577,0.0010508853,0.0002842124,0.00018859864,0.00033122208,0.00084822014,0.00020719566],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.003917825,0.00012072302,0.9335304,0.00005782176,0.002093463,0.001749005,0.0002528209,0.0006072503,0.047209587,0.0003816921,0.00027677976,0.009802617],"study_design_scores_gemma":[0.000077257326,0.00018228365,0.99342877,0.000017032715,0.0006714151,0.002189416,0.00007605717,0.0007853913,0.0017489679,0.00042515405,0.00037999294,0.0000183331],"about_ca_topic_score_codex":0.0014877724,"about_ca_topic_score_gemma":0.0018185473,"teacher_disagreement_score":0.0025241924,"about_ca_system_score_codex":0.00013893892,"about_ca_system_score_gemma":0.00014443604,"threshold_uncertainty_score":0.008444309},"labels":[],"label_agreement":null},{"id":"W2133920348","doi":"10.1038/ng.2271","title":"Detectable clonal mosaicism from birth to old age and its relationship to cancer","year":2012,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Genomic variations and chromosomal abnormalities","field":"Biochemistry, Genetics and Molecular Biology","cited_by":599,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of British Columbia","funders":"National Institute of Dental and Craniofacial Research; National Institute of General Medical Sciences; National Eye Institute; National Center for Advancing Translational Sciences; National Human Genome Research Institute; National Heart, Lung, and Blood Institute; National Institute on Drug Abuse; Howard Hughes Medical Institute; U.S. Public Health Service; National Institute on Alcohol Abuse and Alcoholism; National Cancer Institute; National Institutes of Health","keywords":"Biology; Genetics; Cancer","score_opus":0.011320509595992505,"score_gpt":0.2530454206873507,"score_spread":0.24172491109135819,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2133920348","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9966217,0.0018658723,0.00039038886,0.000053119496,0.000008089902,0.0000033239444,0.00023723782,0.000015670827,0.00080453005],"genre_scores_gemma":[0.99899524,0.000425507,0.000119938406,0.000010091753,0.0000115169905,0.0000025615545,0.00008219069,0.000003924959,0.00034902222],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99986815,0.000025521871,0.000011757163,0.000033722463,0.000026322256,0.000034463745],"domain_scores_gemma":[0.9988194,0.0004408048,0.0003611479,0.00008946921,0.00011323006,0.00017595984],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00028606888,0.00011645425,0.00019676938,0.0016917009,0.00023374148,0.0003771797,0.00028112374,0.00030303898,0.0010853258],"category_scores_gemma":[0.0017745179,0.00018362518,0.00015080534,0.000666967,0.00032886537,0.00023778259,0.00031891704,0.00036205587,0.00013746273],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0024453683,0.00011817493,0.7891211,0.000054227265,0.000057639023,0.006295046,0.00067634304,0.00023769967,0.16460098,0.0008262384,0.00035262268,0.035214685],"study_design_scores_gemma":[0.00000649048,0.00026755955,0.9839626,0.000005923428,0.000027541417,0.007082861,0.00014133632,0.00014969375,0.0072336765,0.00038331782,0.0007276879,0.000011178005],"about_ca_topic_score_codex":0.0012751446,"about_ca_topic_score_gemma":0.0009500761,"teacher_disagreement_score":0.0016917009,"about_ca_system_score_codex":0.00018995581,"about_ca_system_score_gemma":0.00016366653,"threshold_uncertainty_score":0.0036307573},"labels":[],"label_agreement":null},{"id":"W2134544862","doi":"10.1038/ng.2728","title":"Mutations in GRIN2A cause idiopathic focal epilepsy with rolandic spikes","year":2013,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Epilepsy research and treatment","field":"Medicine","cited_by":440,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"McMaster University","funders":"National Heart, Lung, and Blood Institute; Medical Research Council","keywords":"Rolandic epilepsy; Epilepsy; Biology; Exon; Exact test; Audiology; Genetics; Mutation; Epilepsy syndromes; Neuroscience; Medicine; Internal medicine; Gene","score_opus":0.012338053423581,"score_gpt":0.29117775915332106,"score_spread":0.27883970572974004,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2134544862","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.97903377,0.0016070749,0.003990893,0.002927019,0.0004463007,0.00008525848,0.0007685677,0.0002899818,0.010851196],"genre_scores_gemma":[0.9971103,0.00020694321,0.0012781476,0.00036315992,0.00010069259,0.000010924246,0.0001361285,0.00004779193,0.00074597524],"study_design_codex":"case_report","study_design_gemma":"observational","domain_scores_codex":[0.99953663,0.00008167421,0.000075193035,0.00008754111,0.0001296119,0.00008937445],"domain_scores_gemma":[0.99905115,0.00032000744,0.00033171423,0.000046871886,0.00005607461,0.00019415024],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00030319794,0.0019917085,0.00063190947,0.0010229698,0.0006800075,0.00058225397,0.0009279099,0.0027947277,0.002738171],"category_scores_gemma":[0.0015835537,0.0003500751,0.0010211534,0.00080384495,0.0014341002,0.000501483,0.0012314129,0.0009271707,0.00077399204],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0015517918,0.000264765,0.02751959,0.00019018927,0.0004568102,0.8027886,0.00058127934,0.0017393047,0.14235139,0.0037647118,0.003878884,0.014912763],"study_design_scores_gemma":[0.0006888229,0.0003683327,0.08047263,0.00012297343,0.0005180702,0.85349065,0.00060587405,0.004810041,0.04599027,0.0048334883,0.007960423,0.00013838253],"about_ca_topic_score_codex":0.001991178,"about_ca_topic_score_gemma":0.0038619048,"teacher_disagreement_score":0.0027947277,"about_ca_system_score_codex":0.0007947073,"about_ca_system_score_gemma":0.0006322125,"threshold_uncertainty_score":0.009160101},"labels":[],"label_agreement":null},{"id":"W2135176038","doi":"10.1038/ng.2408","title":"Common variants at the MHC locus and at chromosome 16q24.1 predispose to Barrett's esophagus","year":2012,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Esophageal Cancer Research and Treatment","field":"Medicine","cited_by":170,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Saskatchewan; Princess Margaret Cancer Centre; University of Toronto; McMaster University Medical Centre; University Health Network","funders":"National Cancer Institute; National Institute for Health and Care Research; Cancer Research UK; Wellcome Trust","keywords":"Biology; Locus (genetics); Genetics; Barrett's esophagus; Esophagus; Major histocompatibility complex; Gene; Anatomy","score_opus":0.012741033004181578,"score_gpt":0.3099454067774949,"score_spread":0.2972043737733133,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2135176038","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9971578,0.0011676314,0.0002615643,0.00015136175,0.000030935134,0.000010774849,0.00029240086,0.00001543336,0.0009121372],"genre_scores_gemma":[0.9985689,0.00041143966,0.0003154462,0.000032379103,0.00004406099,0.000005862447,0.00020176452,0.0000069241723,0.00041321962],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9996736,0.000064969514,0.00003543418,0.000102916914,0.00006646052,0.00005661437],"domain_scores_gemma":[0.99907756,0.00021462345,0.0004014147,0.00005148963,0.000055431035,0.00019951185],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00026048478,0.00077872537,0.000582664,0.0023728916,0.0005387089,0.00047372514,0.00042167297,0.0010856899,0.0052436823],"category_scores_gemma":[0.0014156576,0.00034719217,0.00054294104,0.0016293406,0.0005377936,0.0002476285,0.00049882225,0.000656229,0.00034764464],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0019190083,0.00012234926,0.907035,0.00011028821,0.0006330122,0.015700042,0.00033726764,0.00046676619,0.06146946,0.0004999356,0.0005827315,0.011124213],"study_design_scores_gemma":[0.000065604385,0.00018829548,0.97590524,0.000055327102,0.00030774134,0.01949577,0.0002130467,0.00030047295,0.0018968718,0.000564387,0.0009885229,0.000018829001],"about_ca_topic_score_codex":0.0024105145,"about_ca_topic_score_gemma":0.0035048204,"teacher_disagreement_score":0.0052436823,"about_ca_system_score_codex":0.00027761722,"about_ca_system_score_gemma":0.00014691491,"threshold_uncertainty_score":0.017541885},"labels":[],"label_agreement":null},{"id":"W2135403800","doi":"10.1038/ng.2770","title":"Analysis of immune-related loci identifies 48 new susceptibility variants for multiple sclerosis","year":2013,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Multiple Sclerosis Research Studies","field":"Medicine","cited_by":1442,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"McGill University and Génome Québec Innovation Centre; McGill University","funders":"National Center for Research Resources; National Cancer Institute; National Institute of Allergy and Infectious Diseases; Medical Research Council; National Institutes of Health; National Institute of Environmental Health Sciences; Institut National de la Santé et de la Recherche Médicale; Karolinska Institutet; Hjärt-Lungfonden; Vetenskapsrådet; Crohn's and Colitis UK; Wellcome Trust; Infrastructures en Biologie Santé et Agronomie; Multiple Sclerosis Society; Knut och Alice Wallenbergs Stiftelse; Stockholms Läns Landsting; National Institute of Neurological Disorders and Stroke; National Institute of General Medical Sciences; National Institute for Health and Care Research","keywords":"Multiple sclerosis; Genome-wide association study; Biology; Genotyping; Genetics; Major histocompatibility complex; Genetic association; 1000 Genomes Project; Single-nucleotide polymorphism; Computational biology; Genotype; Immune system; Gene; Immunology","score_opus":0.04379249974018419,"score_gpt":0.3179377165219832,"score_spread":0.27414521678179904,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2135403800","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9982364,0.00050599105,0.0004852291,0.00007854091,0.000011068224,0.000009664534,0.00025277122,0.000012072285,0.0004081957],"genre_scores_gemma":[0.998338,0.00018618918,0.00079964235,0.000057930367,0.000020005486,0.000011563335,0.00025233254,0.000016809397,0.0003174636],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99913365,0.00022654876,0.000116267285,0.00023444206,0.00014886563,0.00014026919],"domain_scores_gemma":[0.9976648,0.0012773421,0.0005181725,0.00019173682,0.00011581006,0.00023210005],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.000914286,0.00061599736,0.00057278405,0.0021376323,0.0006780971,0.0005937517,0.00067856314,0.00087721075,0.0043588607],"category_scores_gemma":[0.0024404493,0.0002738543,0.0010646234,0.0018518929,0.0005462981,0.00028859655,0.0005718689,0.00070095493,0.00038777455],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0070405174,0.0005276985,0.78832173,0.00027358966,0.002236499,0.008396314,0.0018255775,0.00059763837,0.14678226,0.00080861547,0.0008115551,0.042378027],"study_design_scores_gemma":[0.00033919566,0.00045202993,0.98474634,0.000053154738,0.0008396261,0.003504717,0.0002650258,0.00040550143,0.007024488,0.00054077577,0.0018034872,0.000025666108],"about_ca_topic_score_codex":0.0021685564,"about_ca_topic_score_gemma":0.0037034487,"teacher_disagreement_score":0.0043588607,"about_ca_system_score_codex":0.00021595601,"about_ca_system_score_gemma":0.00021941758,"threshold_uncertainty_score":0.014581859},"labels":[],"label_agreement":null},{"id":"W2135456872","doi":"10.1038/ng.450","title":"Identification of seven new prostate cancer susceptibility loci through a genome-wide association study","year":2009,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Genetic Associations and Epidemiology","field":"Biochemistry, Genetics and Molecular Biology","cited_by":424,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"McGill University","funders":"Cancer Research UK; National Institutes of Health; National Cancer Institute; National Institute for Health and Care Research; National Center for Research Resources; National Institute of General Medical Sciences","keywords":"Prostate cancer; Single-nucleotide polymorphism; Genome-wide association study; Biology; Cancer; Allele; Genetics; Genetic association; Prostate; Disease; Case-control study; Oncology; Internal medicine; Genotype; Gene; Medicine","score_opus":0.009683734133261386,"score_gpt":0.3003182376191301,"score_spread":0.2906345034858687,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2135456872","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99740416,0.00035330316,0.0014028529,0.00013224296,0.00001438896,0.00002747246,0.00021285439,0.000022324773,0.00043043905],"genre_scores_gemma":[0.99773693,0.00018919402,0.0013897761,0.000076475924,0.000015744148,0.000018626059,0.00028658586,0.000011734811,0.00027500335],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99858177,0.0002929603,0.00014138721,0.00044886855,0.0003309471,0.00020406762],"domain_scores_gemma":[0.9970125,0.0012778527,0.00053915766,0.00029559294,0.00039934952,0.00047558127],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0017282795,0.0005005028,0.00067390274,0.0020257805,0.0011652224,0.0012511631,0.0011880645,0.0008734713,0.0014154656],"category_scores_gemma":[0.0035524992,0.0005527702,0.00087518326,0.0022607385,0.001016384,0.00037358527,0.0009518521,0.0012645953,0.00021204665],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0017151623,0.00037755276,0.94973224,0.00008271885,0.0007994918,0.0032098764,0.00065118965,0.00029578662,0.029131254,0.00045228968,0.00036072693,0.013191648],"study_design_scores_gemma":[0.00022141525,0.00033927307,0.99034566,0.000015546933,0.0007856937,0.0028527852,0.00032987568,0.00060693495,0.0027882345,0.0004585394,0.0012157415,0.000040291037],"about_ca_topic_score_codex":0.0054062977,"about_ca_topic_score_gemma":0.006405611,"teacher_disagreement_score":0.0054062977,"about_ca_system_score_codex":0.000397017,"about_ca_system_score_gemma":0.0010821914,"threshold_uncertainty_score":0.010749638},"labels":[],"label_agreement":null},{"id":"W2135665336","doi":"10.1038/ng.2563","title":"Large-scale genotyping identifies 41 new loci associated with breast cancer risk","year":2013,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Genetic Associations and Epidemiology","field":"Biochemistry, Genetics and Molecular Biology","cited_by":1105,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Royal Victoria Hospital; Centre hospitalier universitaire de Québec; Royal Victoria Regional Health Centre; Université Laval; Université de Montréal; McGill University Health Centre; McGill University; Lunenfeld-Tanenbaum Research Institute; Mount Sinai Hospital; McGill University and Génome Québec Innovation Centre; Public Health Ontario; University Health Network; University of Toronto","funders":"Canadian Institutes of Health Research; National Cancer Institute; National Institute for Health and Care Research; Cancer Research UK","keywords":"Biology; Genotyping; Breast cancer; Genetics; Scale (ratio); Computational biology; Cancer; Genotype; Gene","score_opus":0.005246362570649677,"score_gpt":0.24410605084554632,"score_spread":0.23885968827489665,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2135665336","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9882464,0.0011664759,0.0049991524,0.0004461381,0.000056952056,0.000043187196,0.002973253,0.00011802495,0.001950445],"genre_scores_gemma":[0.9914922,0.0004203147,0.0041947756,0.00026878293,0.00006178606,0.000054787775,0.0019880654,0.000052479467,0.0014668353],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9983341,0.0005154395,0.00010910917,0.00050627225,0.00031827448,0.00021680395],"domain_scores_gemma":[0.99559444,0.002363443,0.0009315511,0.00060051895,0.000193652,0.00031635124],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0012886487,0.00068221707,0.0007658121,0.0016229916,0.0006281991,0.0011291798,0.0007309027,0.0012387643,0.0027252638],"category_scores_gemma":[0.003771461,0.00062185136,0.0008683355,0.002397788,0.00044930988,0.00030102304,0.00062181376,0.0010112412,0.0008254184],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0019724101,0.0003092123,0.85972345,0.00016504616,0.0011315349,0.0013906945,0.00046182162,0.0009715383,0.090811834,0.00059870037,0.001982694,0.040480997],"study_design_scores_gemma":[0.00008758781,0.000094828,0.99117774,0.000017811046,0.0002978816,0.00088392495,0.000074725234,0.0006242321,0.003968459,0.0005341917,0.0022136471,0.000024983337],"about_ca_topic_score_codex":0.0024846818,"about_ca_topic_score_gemma":0.0048152655,"teacher_disagreement_score":0.0027252638,"about_ca_system_score_codex":0.00030953006,"about_ca_system_score_gemma":0.00029586966,"threshold_uncertainty_score":0.009116948},"labels":[],"label_agreement":null},{"id":"W2136376873","doi":"10.1038/ng.2554","title":"Genome-wide meta-analyses of multiancestry cohorts identify multiple new susceptibility loci for refractive error and myopia","year":2013,"lang":"en","type":"review","venue":"Nature Genetics","topic":"Ophthalmology and Visual Impairment Studies","field":"Medicine","cited_by":486,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"SickKids Foundation; Hospital for Sick Children; University of Toronto","funders":"National Center for Advancing Translational Sciences; Wellcome Trust; National Eye Institute; National Institutes of Health; National Institute of Diabetes and Digestive and Kidney Diseases; National Heart, Lung, and Blood Institute; National Institute for Health and Care Research","keywords":"Refractive error; Genome-wide association study; Meta-analysis; Biology; 1000 Genomes Project; Single-nucleotide polymorphism; Genetics; Genetic association; Bioinformatics; Medicine; Eye disease; Gene; Genotype; Internal medicine","score_opus":0.2434122448984447,"score_gpt":0.502808177774235,"score_spread":0.2593959328757903,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2136376873","genre_codex":"review","genre_gemma":"review","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"review","genre_consensus":"review","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.0016018725,0.997509,0.0002540617,0.00023461689,0.000067214954,0.000008743124,0.00017381771,0.0000079203355,0.00014262229],"genre_scores_gemma":[0.024915123,0.9730166,0.000894983,0.00041308854,0.00016495217,0.000025856729,0.0003832264,0.000006111556,0.00018002985],"study_design_codex":"design_other","study_design_gemma":"meta_analysis","domain_scores_codex":[0.99901843,0.0003451973,0.00020598545,0.000215409,0.0001627938,0.00005216379],"domain_scores_gemma":[0.99658835,0.0026529091,0.00038404146,0.000106953994,0.00021306521,0.000054640823],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0028768908,0.0015912796,0.0047321855,0.0022482227,0.00020321063,0.0009477572,0.0012721447,0.0010344426,0.0022095132],"category_scores_gemma":[0.0055983923,0.0005309674,0.0062083486,0.0032371432,0.0002485991,0.0005991928,0.0008158035,0.001048691,0.00023894985],"study_design_candidate":"meta_analysis","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0027502421,0.00009380449,0.029072985,0.17569178,0.25120276,0.0009669134,0.00021438423,0.0012723638,0.00158428,0.001345312,0.012528596,0.5232766],"study_design_scores_gemma":[0.0013510897,0.0006989519,0.09467187,0.038905036,0.7410055,0.003070288,0.00033946845,0.0006118812,0.0013127271,0.0058667813,0.111955725,0.00021070479],"about_ca_topic_score_codex":0.0033852984,"about_ca_topic_score_gemma":0.009572682,"teacher_disagreement_score":0.0047321855,"about_ca_system_score_codex":0.00054590014,"about_ca_system_score_gemma":0.0013532722,"threshold_uncertainty_score":0.015214622},"labels":[],"label_agreement":null},{"id":"W2136558851","doi":"10.1038/ng.567","title":"Variants in ADCY5 and near CCNL1 are associated with fetal growth and birth weight","year":2010,"lang":"en","type":"review","venue":"Nature Genetics","topic":"Birth, Development, and Health","field":"Medicine","cited_by":258,"is_retracted":false,"has_abstract":false,"route_ca_aff":false,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"","funders":"National Institute of Environmental Health Sciences; National Center for Research Resources; National Institute of Allergy and Infectious Diseases; National Institute of Mental Health; National Heart, Lung, and Blood Institute; National Institute of Child Health and Human Development; National Institute of Diabetes and Digestive and Kidney Diseases; Biocenter, University of Oulu; Münchner Zentrum für Gesundheitswissenschaften, Ludwig-Maximilians-Universität München; Medical Research Council; National Institutes of Health; Erasmus Universiteit Rotterdam; Eunice Kennedy Shriver National Institute of Child Health and Human Development; ZonMw; Raine Medical Research Foundation; British Heart Foundation; Scottish Government; Healthway; Erasmus Medisch Centrum; University of Bristol; Oulun Yliopisto; European Commission; Fogarty International Center; Juvenile Diabetes Research Foundation International; Diabetes UK; Canadian Institutes of Health Research; Royal Society; Bundesministerium für Bildung und Forschung; National Institute for Health and Care Research; National Health and Medical Research Council; Children's Hospital of Philadelphia; Nederlandse Organisatie voor Wetenschappelijk Onderzoek; Wellcome Trust","keywords":"Birth weight; Biology; Genome-wide association study; Single-nucleotide polymorphism; Low birth weight; Pregnancy; Genetic association; Genetics; Allele; Demography; Gene; Genotype","score_opus":0.016924125125013265,"score_gpt":0.2936656755207174,"score_spread":0.2767415503957041,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2136558851","genre_codex":"review","genre_gemma":"review","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"review","genre_consensus":"review","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.0013972152,0.9961442,0.00038462356,0.0006921188,0.00016588099,0.0000033502715,0.00008581583,0.000014350718,0.0011125074],"genre_scores_gemma":[0.009840927,0.98715997,0.00081577885,0.0003786791,0.00034906785,0.00001042642,0.00022118363,0.0000050832537,0.0012188267],"study_design_codex":"design_other","study_design_gemma":"observational","domain_scores_codex":[0.999762,0.00004600007,0.0000356625,0.00005836889,0.000079545825,0.000018544986],"domain_scores_gemma":[0.9995468,0.00027928612,0.00007216072,0.0000107870555,0.000063357526,0.0000275045],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00048823835,0.0010011633,0.0014435621,0.0011239724,0.00015986132,0.00051569537,0.0008437049,0.0009881133,0.0018172693],"category_scores_gemma":[0.00088855985,0.00021465347,0.0003438842,0.0013898179,0.00040354655,0.00037384283,0.00037184687,0.0008256371,0.0006359854],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00044690096,0.000045528846,0.005974769,0.0050601484,0.00047247767,0.0022030626,0.00006046307,0.0007100212,0.0030426788,0.002488744,0.026304057,0.9531911],"study_design_scores_gemma":[0.00020437283,0.00014580316,0.03648084,0.0045107254,0.0016142888,0.018063158,0.0001918128,0.0006841126,0.0028449576,0.0057643782,0.929412,0.000083549356],"about_ca_topic_score_codex":0.0031865707,"about_ca_topic_score_gemma":0.004323553,"teacher_disagreement_score":0.0031865707,"about_ca_system_score_codex":0.00059739116,"about_ca_system_score_gemma":0.00059460715,"threshold_uncertainty_score":0.006336093},"labels":[],"label_agreement":null},{"id":"W2137186819","doi":"10.1038/ng.424","title":"A genome-wide association study identifies a new ovarian cancer susceptibility locus on 9p22.2","year":2009,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Ovarian cancer diagnosis and treatment","field":"Medicine","cited_by":311,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Coalition for Research in Women's Health; Lunenfeld-Tanenbaum Research Institute","funders":"National Cancer Institute; National Institute for Health and Care Research; Cancer Research UK; Wellcome Trust","keywords":"Genome-wide association study; Single-nucleotide polymorphism; Ovarian cancer; Odds ratio; Biology; Locus (genetics); SNP; Genetic association; Genetics; Oncology; Cancer; Genotype; Internal medicine; Medicine; Gene","score_opus":0.013790097655723612,"score_gpt":0.30670213357997694,"score_spread":0.29291203592425336,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2137186819","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9928986,0.0010547462,0.0022192707,0.00085750024,0.00010462672,0.000040412742,0.0011220502,0.00008945691,0.0016132717],"genre_scores_gemma":[0.9957468,0.00039179798,0.0015190841,0.00024474825,0.00011351921,0.000035680503,0.00083503657,0.00002959053,0.0010838573],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9994789,0.000102935635,0.00003939983,0.00019547895,0.00010882045,0.000074528114],"domain_scores_gemma":[0.99890256,0.0004914306,0.00026175397,0.00006933746,0.00006784006,0.00020710909],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0005074769,0.00089948456,0.00060817617,0.0016635695,0.0007891095,0.0008223057,0.0007711871,0.0013804599,0.004635785],"category_scores_gemma":[0.0019189178,0.00037950266,0.0008321849,0.0015446498,0.00046599287,0.00017641985,0.0006729926,0.0011820473,0.00051610253],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.007149146,0.00076790375,0.4966452,0.00032889334,0.002056915,0.061752442,0.0009955857,0.0011807306,0.3766161,0.0020142777,0.005364875,0.045127917],"study_design_scores_gemma":[0.0007787953,0.00080997805,0.9221611,0.00007418058,0.0012965886,0.043510463,0.0002871872,0.0017410706,0.018790467,0.001478072,0.00899883,0.00007329579],"about_ca_topic_score_codex":0.002545863,"about_ca_topic_score_gemma":0.003451996,"teacher_disagreement_score":0.004635785,"about_ca_system_score_codex":0.00022505877,"about_ca_system_score_gemma":0.00029475108,"threshold_uncertainty_score":0.0155082345},"labels":[],"label_agreement":null},{"id":"W2139747296","doi":"10.1038/ng.437","title":"Personalized copy number and segmental duplication maps using next-generation sequencing","year":2009,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Genomic variations and chromosomal abnormalities","field":"Biochemistry, Genetics and Molecular Biology","cited_by":776,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Simon Fraser University","funders":"National Human Genome Research Institute; Howard Hughes Medical Institute; National Science Foundation","keywords":"Copy-number variation; Segmental duplication; Biology; Gene duplication; Genome; Structural variation; Sequence (biology); Gene; Genetics; Human genome; Copy number analysis; Computational biology; Constraint (computer-aided design); DNA sequencing; Gene dosage; Gene family; Mathematics","score_opus":0.02391843337455049,"score_gpt":0.26503776939140833,"score_spread":0.24111933601685784,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2139747296","genre_codex":"methods","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":null,"domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.34316242,0.0046578674,0.62281865,0.0017017586,0.0004860828,0.00040540774,0.007988367,0.0059044254,0.012875044],"genre_scores_gemma":[0.5453296,0.0034808426,0.42857885,0.0009870032,0.00025884775,0.00041362294,0.008718518,0.0006965554,0.0115361065],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99955744,0.00007520844,0.000019906882,0.00014836385,0.00016128675,0.000037740614],"domain_scores_gemma":[0.9996371,0.00015731702,0.000042422336,0.00009747981,0.000035479654,0.00003010077],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0006063086,0.0003684198,0.00076409103,0.0008503266,0.00029595965,0.00062661566,0.00054923573,0.00067437266,0.0028058912],"category_scores_gemma":[0.000950078,0.00041718374,0.00056203344,0.0006611147,0.0002310326,0.0005492171,0.00070069276,0.0012089084,0.0007769561],"study_design_candidate":"bench_or_experimental","study_design_consensus":"bench_or_experimental","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00052955496,0.00011847127,0.005796864,0.00024780302,0.00022098019,0.0006512789,0.00011534829,0.00972772,0.6672303,0.005973961,0.0043460145,0.30504176],"study_design_scores_gemma":[0.0003767905,0.0007787575,0.062588945,0.00009456567,0.0010076785,0.010845214,0.00016027759,0.13331616,0.6655146,0.037342664,0.087758206,0.00021619601],"about_ca_topic_score_codex":0.0010014971,"about_ca_topic_score_gemma":0.0023844729,"teacher_disagreement_score":0.0028058912,"about_ca_system_score_codex":0.0004088298,"about_ca_system_score_gemma":0.00036500304,"threshold_uncertainty_score":0.009386659},"labels":[],"label_agreement":null},{"id":"W2139852278","doi":"10.1038/ng.3097","title":"Defining the role of common variation in the genomic and biological architecture of adult human height","year":2014,"lang":"en","type":"review","venue":"Nature Genetics","topic":"Genetic Associations and Epidemiology","field":"Biochemistry, Genetics and Molecular Biology","cited_by":2096,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Institut universitaire de cardiologie et de pneumologie de Québec; Université Laval; Montreal Heart Institute","funders":"Eunice Kennedy Shriver National Institute of Child Health and Human Development; Wellcome Trust; National Human Genome Research Institute; National Center for Advancing Translational Sciences; British Heart Foundation; National Cancer Institute; National Institute of Diabetes and Digestive and Kidney Diseases; National Heart, Lung, and Blood Institute; Novo Nordisk Fonden; National Institute for Health and Care Research; National Institute of General Medical Sciences; Medical Research Council","keywords":"Biology; Genetic architecture; Genetics; Genome-wide association study; Heritability; Phenotype; Gene; Wnt signaling pathway; Missing heritability problem; Single-nucleotide polymorphism; Genetic association; Quantitative trait locus; Genetic variation; Genome; Evolutionary biology; Genotype","score_opus":0.010283564699861534,"score_gpt":0.29372031184382164,"score_spread":0.2834367471439601,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2139852278","genre_codex":"review","genre_gemma":"review","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"review","genre_consensus":"review","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.00012801304,0.9983444,0.00030519397,0.00080869586,0.00014859547,0.000001710064,0.000023722207,0.000003724367,0.00023598522],"genre_scores_gemma":[0.00094865245,0.99779546,0.00026315893,0.0004572012,0.00037113554,0.0000027843807,0.00003495413,0.0000012643542,0.00012548776],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.99959856,0.00008725756,0.000051704355,0.00010272161,0.00012893642,0.0000308368],"domain_scores_gemma":[0.9978048,0.0015003147,0.00021876143,0.000054858137,0.00032842922,0.000092805734],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0022069318,0.0009045454,0.0016572396,0.0020506664,0.00025078023,0.0012875256,0.0015991605,0.0019501073,0.0018028687],"category_scores_gemma":[0.0034458665,0.00036652194,0.00052310264,0.002769564,0.0016105897,0.0018053736,0.0014076367,0.0025352128,0.0005589451],"study_design_candidate":"not_applicable","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00012093946,0.000031014242,0.0018303073,0.009104234,0.00027355662,0.00028639002,0.000093391616,0.0006547969,0.0011280354,0.011534938,0.01847114,0.95647115],"study_design_scores_gemma":[0.00005587762,0.0001052101,0.011611473,0.008608293,0.00068621663,0.0022850516,0.00030654826,0.0003879852,0.00082860485,0.03186965,0.9431568,0.00009836079],"about_ca_topic_score_codex":0.0037870544,"about_ca_topic_score_gemma":0.0044006603,"teacher_disagreement_score":0.0037870544,"about_ca_system_score_codex":0.0008873326,"about_ca_system_score_gemma":0.0021639029,"threshold_uncertainty_score":0.011671543},"labels":[],"label_agreement":null},{"id":"W2140529609","doi":"10.1038/ng1824","title":"Mutations in sodium-borate cotransporter SLC4A11 cause recessive congenital hereditary endothelial dystrophy (CHED2)","year":2006,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Magnesium in Health and Disease","field":"Nursing","cited_by":296,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Alberta","funders":"National Medical Research Council; Singapore Eye Research Institute","keywords":"Biology; Genetics; Corneal dystrophy; Nonsense mutation; Gene; Mutation; Dystrophy; Cotransporter; Missense mutation; Sodium; Chemistry; Cornea","score_opus":0.00903049684640336,"score_gpt":0.27019360838218537,"score_spread":0.26116311153578203,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2140529609","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.98866767,0.00091546256,0.0026010103,0.001075587,0.00029172283,0.000044564604,0.00083562743,0.00021423103,0.005354152],"genre_scores_gemma":[0.99373865,0.00030760298,0.0017226321,0.00022833969,0.00006706321,0.000014784245,0.00026723073,0.000067604145,0.003586099],"study_design_codex":"case_report","study_design_gemma":"observational","domain_scores_codex":[0.9996031,0.00005497069,0.000053899694,0.00009969125,0.0001262773,0.00006209121],"domain_scores_gemma":[0.9993118,0.0002489217,0.00014964578,0.00002783058,0.000064589236,0.00019726098],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00025151487,0.001876164,0.00058871764,0.0009866116,0.000752665,0.00042126275,0.00061337074,0.0019074687,0.004047174],"category_scores_gemma":[0.0012170387,0.00031961288,0.00051332393,0.00069148454,0.0009209057,0.00029740503,0.0008649465,0.00091719115,0.00055408315],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0015166916,0.0002648181,0.04772095,0.0003362528,0.0004944482,0.6206448,0.0010598297,0.0009633612,0.2971375,0.0032100126,0.007469477,0.019181838],"study_design_scores_gemma":[0.00072765717,0.0006335916,0.18537953,0.00021692888,0.00073384383,0.66374207,0.0011376792,0.006128341,0.115834616,0.0017630924,0.023527814,0.00017479832],"about_ca_topic_score_codex":0.004660274,"about_ca_topic_score_gemma":0.006102659,"teacher_disagreement_score":0.004660274,"about_ca_system_score_codex":0.0006627827,"about_ca_system_score_gemma":0.00055904285,"threshold_uncertainty_score":0.013539195},"labels":[],"label_agreement":null},{"id":"W2141297584","doi":"10.1038/ng.1054","title":"Toward interoperable bioscience data","year":2012,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Biomedical Text Mining and Ontologies","field":"Biochemistry, Genetics and Molecular Biology","cited_by":468,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Ontario Institute for Cancer Research","funders":"National Cancer Institute; National Heart, Lung, and Blood Institute; National Human Genome Research Institute; National Center for Research Resources; National Institute of General Medical Sciences; National Institute of Mental Health; Biotechnology and Biological Sciences Research Council","keywords":"Interoperability; Biology; Data science; Knowledge management; Data curation; Research data; World Wide Web; Computer science","score_opus":0.050154971685411776,"score_gpt":0.3283915047080819,"score_spread":0.27823653302267015,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2141297584","genre_codex":"methods","genre_gemma":"empirical","domain_codex":null,"domain_gemma":"reproducibility","model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":null,"domain_candidate":"reproducibility","domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.003754554,0.0010709994,0.9586614,0.019514102,0.0006145621,0.00040093673,0.0025777372,0.0038742174,0.009531468],"genre_scores_gemma":[0.0371897,0.0017968249,0.9360473,0.005155799,0.00049465563,0.0007945852,0.014688757,0.0008981344,0.0029342796],"study_design_codex":"theoretical_or_conceptual","study_design_gemma":"theoretical_or_conceptual","domain_scores_codex":[0.9410763,0.024195552,0.009593097,0.008508712,0.014379534,0.0022469233],"domain_scores_gemma":[0.8088862,0.03817484,0.006903705,0.1155645,0.022435376,0.008035413],"candidate_categories":["metaresearch","open_science"],"consensus_categories":[],"category_scores_codex":[0.09935374,0.0015589821,0.0027770465,0.011836438,0.0040406077,0.019215234,0.010122755,0.0063484046,0.0038031172],"category_scores_gemma":[0.113306284,0.0020237947,0.004433376,0.0147191845,0.008132686,0.0443039,0.038855687,0.0149475075,0.0029401807],"study_design_candidate":"theoretical_or_conceptual","study_design_consensus":"theoretical_or_conceptual","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00013101556,0.0002053959,0.0027866564,0.0006373949,0.00022302427,0.00032877622,0.002584997,0.004512328,0.00258558,0.85909677,0.022886135,0.10402195],"study_design_scores_gemma":[0.000046871584,0.000042319436,0.0006206969,0.0006108481,0.00011818009,0.00017963431,0.0010777469,0.012577693,0.0028710577,0.76883304,0.21294743,0.000074460295],"about_ca_topic_score_codex":0.0054552034,"about_ca_topic_score_gemma":0.0047261594,"teacher_disagreement_score":0.9898772,"about_ca_system_score_codex":0.004932616,"about_ca_system_score_gemma":0.018728321,"threshold_uncertainty_score":0.525439},"labels":[],"label_agreement":null},{"id":"W2141550398","doi":"10.1038/ng.919","title":"The genome of the mesopolyploid crop species Brassica rapa","year":2011,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Chromosomal and Genetic Variations","field":"Agricultural and Biological Sciences","cited_by":2205,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Agriculture and Agri-Food Canada; Plant Biotechnology Institute","funders":"Directorate for Biological Sciences; Universität Bielefeld; Ministry for Food, Agriculture, Forestry and Fisheries; Rural Development Administration; Biotechnology and Biological Sciences Research Council; Ministry of Science and Technology of the People's Republic of China; Grains Research and Development Corporation; Government of Jiangxi Province; National Natural Science Foundation of China; European Commission","keywords":"Biology; Brassica rapa; Genome; Crop; Brassica; Genetics; Botany; Agronomy; Gene","score_opus":0.018619285245148436,"score_gpt":0.20209148702373894,"score_spread":0.1834722017785905,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2141550398","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99425745,0.0015214363,0.00072400866,0.00011344816,0.000008504847,0.000004697925,0.0018206108,0.00004588019,0.0015039498],"genre_scores_gemma":[0.9924648,0.0007084952,0.00093530916,0.000063422995,0.00000912073,0.0000063623065,0.003925863,0.000023059421,0.0018636506],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9999589,0.0000054452403,0.0000019850552,0.00001795724,0.000010116893,0.000005610851],"domain_scores_gemma":[0.99990094,0.000034984256,0.000025709347,0.00001269891,0.000009921918,0.000015749341],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.000042592517,0.00014756594,0.00011416146,0.00029452326,0.00021968302,0.00019136998,0.00013249641,0.0002534242,0.0007948936],"category_scores_gemma":[0.00016919411,0.00011800952,0.00012907073,0.00028883986,0.00012646987,0.00015309177,0.00015724408,0.00029484354,0.00023606961],"study_design_candidate":"bench_or_experimental","study_design_consensus":"bench_or_experimental","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00011384891,0.0000038303124,0.0013966466,0.000037086746,0.000010130292,0.0000546277,0.00008206394,0.000073359595,0.9938797,0.00014846885,0.000061053994,0.004139086],"study_design_scores_gemma":[0.000062866,0.0004507467,0.61589426,0.00005764585,0.00024411551,0.0027509655,0.00059871736,0.001605223,0.34567684,0.0012669595,0.03135471,0.000036861096],"about_ca_topic_score_codex":0.002461283,"about_ca_topic_score_gemma":0.0037482188,"teacher_disagreement_score":0.002461283,"about_ca_system_score_codex":0.00015711325,"about_ca_system_score_gemma":0.00010844573,"threshold_uncertainty_score":0.0048938394},"labels":[],"label_agreement":null},{"id":"W2141642891","doi":"10.1038/ng.609","title":"Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis","year":2010,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Genetic Associations and Epidemiology","field":"Biochemistry, Genetics and Molecular Biology","cited_by":1797,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"McGill University; McGill University and Génome Québec Innovation Centre; Ontario Institute for Cancer Research","funders":"National Center for Research Resources; National Institute of Arthritis and Musculoskeletal and Skin Diseases; National Human Genome Research Institute; National Institutes of Health; National Institute of Diabetes and Digestive and Kidney Diseases; National Heart, Lung, and Blood Institute; National Institute for Health and Care Research; National Institute on Drug Abuse; Wellcome Trust","keywords":"Biology; Genome-wide association study; Locus (genetics); Genetics; Type 2 diabetes; Genetic association; Gene; 1000 Genomes Project; Single-nucleotide polymorphism; Diabetes mellitus; Genotype; Endocrinology","score_opus":0.006084929744045815,"score_gpt":0.27643140613816924,"score_spread":0.2703464763941234,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2141642891","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9936413,0.0010325285,0.003777381,0.00013593359,0.000025799389,0.00003438831,0.0005659316,0.000057792768,0.0007288206],"genre_scores_gemma":[0.9936226,0.00038385723,0.0045676413,0.00008545831,0.000022634289,0.000040624895,0.0007090823,0.00001760341,0.00055050233],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9988456,0.00037168243,0.00015929325,0.00031251076,0.0001790938,0.00013179341],"domain_scores_gemma":[0.99590236,0.0022257448,0.00075845537,0.0004045099,0.00028641266,0.00042257478],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0017574221,0.00050921715,0.00077892916,0.0016356893,0.0008400425,0.0008959276,0.0007257111,0.0007049604,0.0023020806],"category_scores_gemma":[0.0046325093,0.0004610144,0.00073411484,0.0029379185,0.0006345154,0.00025973286,0.0008118416,0.00072435034,0.00033688053],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0063835504,0.00046056428,0.8577859,0.00030798273,0.001805634,0.0031373522,0.00067080435,0.00095303525,0.07345526,0.00063187745,0.001113045,0.05329503],"study_design_scores_gemma":[0.00041366913,0.00031486645,0.9880521,0.00003761164,0.0010628711,0.0017057824,0.00029611762,0.0009198597,0.0041448814,0.00081438373,0.0021934486,0.000044482695],"about_ca_topic_score_codex":0.002263649,"about_ca_topic_score_gemma":0.0049735093,"teacher_disagreement_score":0.0023020806,"about_ca_system_score_codex":0.00024639396,"about_ca_system_score_gemma":0.00045759176,"threshold_uncertainty_score":0.0092942715},"labels":[],"label_agreement":null},{"id":"W2142054160","doi":"10.1038/ng0106-3","title":"A road map for efficient and reliable human genome epidemiology","year":2006,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Genetic Associations and Epidemiology","field":"Biochemistry, Genetics and Molecular Biology","cited_by":244,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Ottawa","funders":"","keywords":"Genome-wide association study; Data science; Biology; Genetic association; Genetic epidemiology; Data sharing; Set (abstract data type); Field (mathematics); Genetic data; Computational biology; Computer science; Genetics; Population; Medicine; Single-nucleotide polymorphism; Environmental health; Gene","score_opus":0.010890542026115148,"score_gpt":0.28796432319192705,"score_spread":0.2770737811658119,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2142054160","genre_codex":"methods","genre_gemma":"methods","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"methods","genre_consensus":"methods","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.0017700434,0.0015257746,0.9774075,0.0036983392,0.0004370475,0.0003188139,0.0038506594,0.007984346,0.00300744],"genre_scores_gemma":[0.027985685,0.0019816058,0.9588723,0.00056279614,0.0003559575,0.0009549107,0.00598004,0.00051602494,0.0027906129],"study_design_codex":"design_other","study_design_gemma":"theoretical_or_conceptual","domain_scores_codex":[0.99741447,0.001119529,0.00028964924,0.00038304433,0.00064684276,0.00014647149],"domain_scores_gemma":[0.98030657,0.008203865,0.0009311445,0.0029585883,0.00670535,0.0008943655],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00541209,0.0013175813,0.0023567462,0.0058707963,0.0016437959,0.0045624115,0.0025175929,0.0028726591,0.022238754],"category_scores_gemma":[0.039158195,0.0014661254,0.0012346462,0.004417426,0.0008857379,0.0049481476,0.004049014,0.0031511725,0.012491559],"study_design_candidate":"theoretical_or_conceptual","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00041188748,0.0001981149,0.004624532,0.0010912679,0.00024740663,0.00047213948,0.000307894,0.048057076,0.0024254906,0.09950043,0.12398356,0.7186801],"study_design_scores_gemma":[0.00029023606,0.00026421505,0.00459246,0.0005671031,0.000306866,0.0007894718,0.00041101486,0.1794712,0.0030558296,0.51835775,0.29169303,0.00020086415],"about_ca_topic_score_codex":0.012262459,"about_ca_topic_score_gemma":0.0076366398,"teacher_disagreement_score":0.022238754,"about_ca_system_score_codex":0.0015000362,"about_ca_system_score_gemma":0.0063944138,"threshold_uncertainty_score":0.074396074},"labels":[],"label_agreement":null},{"id":"W2142627450","doi":"10.1038/ng.2406","title":"Loss-of-function mutations in HINT1 cause axonal neuropathy with neuromyotonia","year":2012,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":129,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"London Health Sciences Centre; Western University","funders":"National Institute of Neurological Disorders and Stroke","keywords":"Neuromyotonia; Biology; Loss function; Function (biology); Neuroscience; Genetics; Phenotype; Gene","score_opus":0.024944830254755954,"score_gpt":0.2671345386423552,"score_spread":0.24218970838759923,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2142627450","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.993586,0.000649092,0.001447845,0.00037228514,0.000091379465,0.000032250486,0.00031308827,0.00013851891,0.0033696601],"genre_scores_gemma":[0.99782604,0.00015697404,0.00088074995,0.000073929834,0.000028772016,0.0000074582154,0.0000678404,0.000025685498,0.0009324094],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.99983144,0.000025266629,0.000029337207,0.000027405644,0.00005344356,0.000033191838],"domain_scores_gemma":[0.99959725,0.00012648026,0.00011317751,0.000017882827,0.000029574392,0.00011560527],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00018335416,0.0015733037,0.00040880352,0.0008858842,0.0005305012,0.00038421425,0.0006309902,0.001325639,0.0023857425],"category_scores_gemma":[0.0006905477,0.00028665178,0.00043696858,0.00042722767,0.00084283226,0.0002774304,0.00061726477,0.0005705938,0.00045689804],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0028406568,0.00037125754,0.053312145,0.00041567435,0.0004765603,0.3537168,0.0005598297,0.0038939384,0.5565615,0.0031980772,0.003291366,0.021362178],"study_design_scores_gemma":[0.00046793453,0.0009923643,0.3465163,0.0001412901,0.0011327629,0.44024885,0.0007634113,0.010257655,0.1896324,0.002976311,0.006668105,0.00020265023],"about_ca_topic_score_codex":0.0024723187,"about_ca_topic_score_gemma":0.00389515,"teacher_disagreement_score":0.0024723187,"about_ca_system_score_codex":0.00046422187,"about_ca_system_score_gemma":0.00033688036,"threshold_uncertainty_score":0.007981062},"labels":[],"label_agreement":null},{"id":"W2142808441","doi":"10.1038/ng.662","title":"Candidate exome capture identifies mutation of SDCCAG8 as the cause of a retinal-renal ciliopathy","year":2010,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Genetic and Kidney Cyst Diseases","field":"Biochemistry, Genetics and Molecular Biology","cited_by":318,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Montreal Children's Hospital; McGill University Health Centre","funders":"Eunice Kennedy Shriver National Institute of Child Health and Human Development; National Institutes of Health; Retina France; Canadian Institutes of Health Research; Else Kröner-Fresenius-Stiftung; Institut National de la Santé et de la Recherche Médicale; National Eye Institute; Nederlandse Organisatie voor Wetenschappelijk Onderzoek; Wellcome Trust; National Institute of Diabetes and Digestive and Kidney Diseases; James N. Kirby Foundation; Research to Prevent Blindness; F. M. Kirby Foundation","keywords":"Ciliopathy; Ciliopathies; Biology; Joubert syndrome; Exome sequencing; Disease gene identification; Genetics; Nephronophthisis; Cilium; Exome; Mutation; Gene","score_opus":0.003728676733835537,"score_gpt":0.24561041470941994,"score_spread":0.2418817379755844,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2142808441","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99620545,0.00020067536,0.0012145863,0.00030026556,0.000044981523,0.000027937762,0.0005546095,0.00004776819,0.0014036224],"genre_scores_gemma":[0.9975926,0.00006508213,0.0010136309,0.00013051897,0.00001637862,0.000008322975,0.00029908356,0.000017560791,0.0008568925],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.99976486,0.000022569173,0.00002408996,0.00006645873,0.000068896814,0.00005309943],"domain_scores_gemma":[0.99962664,0.00018540646,0.000045622863,0.00002293742,0.00004324836,0.0000761459],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00018335924,0.0006702135,0.00040427293,0.0010632606,0.00065375917,0.00046885514,0.0004417024,0.0016517454,0.0034303537],"category_scores_gemma":[0.0007837632,0.00014470611,0.00047648407,0.00046193553,0.0003647441,0.0002163641,0.00053003064,0.00055331475,0.00044574094],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0014502789,0.00018134427,0.0832738,0.00013359645,0.00018658872,0.39550206,0.0004807097,0.0009613296,0.4937021,0.0015196573,0.0022119163,0.02039663],"study_design_scores_gemma":[0.00018799724,0.00048019408,0.32411286,0.00008915517,0.00033511416,0.44402173,0.0005251091,0.015815718,0.20461328,0.0013152339,0.008430009,0.00007348995],"about_ca_topic_score_codex":0.0024553055,"about_ca_topic_score_gemma":0.0041148583,"teacher_disagreement_score":0.0034303537,"about_ca_system_score_codex":0.0004099501,"about_ca_system_score_gemma":0.00025328988,"threshold_uncertainty_score":0.011475742},"labels":[],"label_agreement":null},{"id":"W2143244825","doi":"10.1038/ng1564","title":"Epistasis between mouse Klra and major histocompatibility complex class I loci is associated with a new mechanism of natural killer cell–mediated innate resistance to cytomegalovirus infection","year":2005,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Immune Cell Function and Interaction","field":"Immunology and Microbiology","cited_by":149,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Institut National de la Recherche Scientifique; Montreal Clinical Research Institute; McGill University","funders":"National Cancer Institute","keywords":"Biology; Major histocompatibility complex; Innate immune system; Mechanism (biology); Immunology; Natural killer cell; Epistasis; Cytomegalovirus; Genetics; Virology; Immune system; Gene; Virus; Herpesviridae; Cytotoxic T cell; Viral disease; In vitro","score_opus":0.012342205907678731,"score_gpt":0.24250310444896975,"score_spread":0.23016089854129101,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2143244825","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9952761,0.00035767676,0.003116018,0.00008313732,0.000019584879,0.000010006393,0.00019665348,0.00023133775,0.0007094391],"genre_scores_gemma":[0.99689204,0.00012547639,0.001498562,0.000066750945,0.0000163913,0.000013704381,0.00021169429,0.0000712547,0.0011042771],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9994337,0.00010625834,0.00006125073,0.00016145805,0.00014386779,0.000093441275],"domain_scores_gemma":[0.9992907,0.000121684934,0.0003174279,0.00010222741,0.00003139768,0.00013638858],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00028391936,0.000715867,0.00040497206,0.0010688229,0.00020675379,0.00059151213,0.00069595006,0.00045019345,0.0019114164],"category_scores_gemma":[0.00038929458,0.0005664274,0.0004253693,0.0003628076,0.00056553783,0.00025332754,0.000683081,0.0008977186,0.00047083476],"study_design_candidate":"bench_or_experimental","study_design_consensus":"bench_or_experimental","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.000113004346,0.000010962647,0.0005069727,0.000009274396,0.00000875051,0.000081191945,0.000006907517,0.00004360688,0.9985448,0.00017599233,0.000026729103,0.00047177717],"study_design_scores_gemma":[0.00024511552,0.0005053483,0.1338093,0.000017810666,0.00022651433,0.0058678,0.00010294294,0.00545879,0.8497125,0.0011257251,0.0028609748,0.00006722079],"about_ca_topic_score_codex":0.0003749561,"about_ca_topic_score_gemma":0.0011058332,"teacher_disagreement_score":0.0019114164,"about_ca_system_score_codex":0.00036575177,"about_ca_system_score_gemma":0.00020930993,"threshold_uncertainty_score":0},"labels":[],"label_agreement":null},{"id":"W2143286837","doi":"10.1038/ng.970","title":"Genome-wide association study identifies loci influencing concentrations of liver enzymes in plasma","year":2011,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Liver Disease Diagnosis and Treatment","field":"Medicine","cited_by":595,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Toronto General Hospital; Lunenfeld-Tanenbaum Research Institute; Mount Sinai Hospital; Toronto Western Hospital; University of Toronto","funders":"National Heart, Lung, and Blood Institute; National Institute on Alcohol Abuse and Alcoholism; National Institute of Diabetes and Digestive and Kidney Diseases; Biocenter, University of Oulu; Helmholtz Zentrum München; Jenny ja Antti Wihurin Rahasto; Medical Research Council; National Institutes of Health; Novo Nordisk Fonden; Instrumentariumin Tiedesäätiö; Universitair Medisch Centrum Groningen; Vetenskapsrådet; National Institute of Mental Health; Stockholms Läns Landsting; Karolinska Institutet; Novo Nordisk; Hjärt-Lungfonden; Biomedicum Helsinki-säätiö; Diabetes Fonds; Rijksuniversiteit Groningen; Oulun Yliopisto; Torsten Söderbergs Stiftelse; Schweizerischer Nationalfonds zur Förderung der Wissenschaftlichen Forschung; European Science Foundation; School of Medicine, Boston University; European Commission; Bundesministerium für Bildung und Forschung; National Institute for Health and Care Research; British Heart Foundation; Cancer Research UK; Imperial College Healthcare NHS Trust; Wellcome Trust; Erasmus Medisch Centrum; Directorate for Biological Sciences; Imperial College London; GlaxoSmithKline; National Science Foundation; Knut och Alice Wallenbergs Stiftelse; Nierstichting; Yrjö Jahnssonin Säätiö; AstraZeneca","keywords":"Biology; Candidate gene; Genome-wide association study; Genetics; Gene; Genetic association; KEGG; Single-nucleotide polymorphism; Transcriptome; Gene expression; Genotype","score_opus":0.016874246227599816,"score_gpt":0.2600229057262388,"score_spread":0.243148659498639,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2143286837","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99777955,0.000522542,0.00072944927,0.00017131468,0.000022540084,0.0000064332794,0.0002688753,0.000025915882,0.00047335253],"genre_scores_gemma":[0.9989911,0.000108359105,0.0004000089,0.000042677744,0.00001939471,0.0000051347265,0.00014961373,0.000009881486,0.00027389466],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9990018,0.00040278776,0.00008394277,0.00030134313,0.00011448106,0.00009567841],"domain_scores_gemma":[0.99832815,0.000735844,0.000449919,0.00017783072,0.000106558655,0.0002016849],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0009922434,0.0007310459,0.00051403564,0.0012740077,0.00059302413,0.00085687544,0.000625561,0.0010703274,0.0020454542],"category_scores_gemma":[0.001953892,0.00050078414,0.0010438225,0.0018345559,0.0005905832,0.00030997506,0.00046745568,0.0011223471,0.00022026882],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0052053193,0.0002562662,0.9525711,0.000060693095,0.0025191882,0.0013838382,0.0002810181,0.00027317042,0.031006256,0.00026591012,0.000522809,0.005654382],"study_design_scores_gemma":[0.0000963594,0.00021553872,0.99645245,0.0000054218985,0.00055680354,0.00078801025,0.000074192554,0.00048045718,0.00092742854,0.00016174988,0.00023094528,0.000010691079],"about_ca_topic_score_codex":0.0034668914,"about_ca_topic_score_gemma":0.003092685,"teacher_disagreement_score":0.0034668914,"about_ca_system_score_codex":0.00025513483,"about_ca_system_score_gemma":0.00029476034,"threshold_uncertainty_score":0.006893456},"labels":[],"label_agreement":null},{"id":"W2143350483","doi":"10.1038/ng.3176","title":"High-density mapping of the MHC identifies a shared role for HLA-DRB1*01:03 in inflammatory bowel diseases and heterozygous advantage in ulcerative colitis","year":2015,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Inflammatory Bowel Disease","field":"Biochemistry, Genetics and Molecular Biology","cited_by":379,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Université de Montréal; Montreal Heart Institute","funders":"National Institute of Diabetes and Digestive and Kidney Diseases; National Institute of Allergy and Infectious Diseases; National Center for Advancing Translational Sciences; Leona M. and Harry B. Helmsley Charitable Trust; Medical Research Council; National Cancer Institute; National Institute of Dental and Craniofacial Research; Seventh Framework Programme; Exzellenzclusters Entzündungsforschung; Agency for Healthcare Research and Quality; Crohn's and Colitis UK; National Institute for Health and Care Research; Bundesministerium für Bildung und Forschung; Deutsche Forschungsgemeinschaft; Institut National Du Cancer; National Health and Medical Research Council; NIHR Cambridge Biomedical Research Centre; Multiple Sclerosis Society; Academy of Medical Sciences; National Institute of Neurological Disorders and Stroke; University of Pittsburgh; Wellcome Trust; Frederick National Laboratory for Cancer Research; European Commission; National Institutes of Health; U.S. Department of Health and Human Services","keywords":"Ulcerative colitis; Biology; Inflammatory bowel disease; Human leukocyte antigen; Inflammatory Bowel Diseases; Major histocompatibility complex; Immunology; Genetics; Internal medicine; Antigen; Disease; Medicine","score_opus":0.006087171765397476,"score_gpt":0.23597429294111874,"score_spread":0.22988712117572127,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2143350483","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9986916,0.00016351748,0.00055342424,0.00005109122,0.000006427999,0.0000014481346,0.000043949483,0.000006399795,0.00048198804],"genre_scores_gemma":[0.99928695,0.000038103102,0.0003907386,0.000021934384,0.0000052941273,0.000001662148,0.000037776957,0.000007655979,0.0002100509],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9997913,0.000059290876,0.00001919359,0.000042591368,0.000044680262,0.000042974323],"domain_scores_gemma":[0.9997037,0.00008993895,0.00008195168,0.000031764313,0.000018918166,0.00007357459],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00024236267,0.0002043537,0.00021211902,0.00064361724,0.00026726665,0.00032991642,0.00028706886,0.00034393405,0.0027682604],"category_scores_gemma":[0.00039784465,0.00020696265,0.0002324017,0.00031934393,0.00026027302,0.00012757268,0.0004028399,0.00042334426,0.00031282243],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0008884274,0.00005473563,0.029753437,0.000027205006,0.000062174964,0.00087000243,0.000100902995,0.0000671285,0.9638265,0.0004872168,0.000116641895,0.0037456937],"study_design_scores_gemma":[0.00014541238,0.00037820693,0.8886552,0.000022331868,0.00016103192,0.011387466,0.00046378362,0.0017112872,0.094420254,0.0009463658,0.0016851756,0.00002360052],"about_ca_topic_score_codex":0.0005446183,"about_ca_topic_score_gemma":0.00075536995,"teacher_disagreement_score":0.0027682604,"about_ca_system_score_codex":0.00008886644,"about_ca_system_score_gemma":0.000049018698,"threshold_uncertainty_score":0.009260714},"labels":[],"label_agreement":null},{"id":"W2146230109","doi":"10.1038/ng1842","title":"Mutations in genes encoding ribonuclease H2 subunits cause Aicardi-Goutières syndrome and mimic congenital viral brain infection","year":2006,"lang":"en","type":"article","venue":"Nature Genetics","topic":"interferon and immune responses","field":"Immunology and Microbiology","cited_by":673,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Hospital for Sick Children","funders":"","keywords":"Biology; Ribonuclease; Gene; Genetics; Mutation; Immune system; Virology; RNA","score_opus":0.0071154285877817365,"score_gpt":0.24377100013137418,"score_spread":0.23665557154359243,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2146230109","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9967325,0.00030445284,0.0008731226,0.00015759251,0.000052876916,0.000022221531,0.00014136973,0.00009669897,0.0016192879],"genre_scores_gemma":[0.99867886,0.00013140812,0.00072325626,0.000045630226,0.000028015887,0.000009297205,0.000052137504,0.000025570816,0.00030589337],"study_design_codex":"case_report","study_design_gemma":"observational","domain_scores_codex":[0.99971396,0.000059460406,0.000039767685,0.000054132244,0.000070372735,0.00006234987],"domain_scores_gemma":[0.999059,0.00038507342,0.00026581623,0.00006628993,0.000027438742,0.00019640927],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00021223981,0.0016571932,0.00049312273,0.0014004955,0.0005284557,0.0004679236,0.00067608897,0.0022163296,0.0020313226],"category_scores_gemma":[0.0021051052,0.00044237383,0.00042067585,0.00066410133,0.0015891615,0.00036626434,0.00087238336,0.00093727844,0.0004177355],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.001044992,0.000083615625,0.02905423,0.00010360137,0.00012398126,0.7125603,0.0005634235,0.0009800342,0.2485623,0.001696946,0.0006246449,0.0046018674],"study_design_scores_gemma":[0.00028666883,0.00038630268,0.08716912,0.000033887314,0.00019345873,0.8364986,0.00039010795,0.0030693968,0.06792689,0.0014865411,0.0024816478,0.00007746992],"about_ca_topic_score_codex":0.0012302616,"about_ca_topic_score_gemma":0.0014835664,"teacher_disagreement_score":0.0022163296,"about_ca_system_score_codex":0.00049325154,"about_ca_system_score_gemma":0.00030314474,"threshold_uncertainty_score":0.006795466},"labels":[],"label_agreement":null},{"id":"W2147311167","doi":"10.1038/ng.686","title":"Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index","year":2010,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Regulation of Appetite and Obesity","field":"Neuroscience","cited_by":2979,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Université de Montréal; McMaster University; Montreal Heart Institute","funders":"National Institute of Arthritis and Musculoskeletal and Skin Diseases; National Center for Research Resources; National Institute of General Medical Sciences; National Human Genome Research Institute; National Institute on Drug Abuse; National Heart, Lung, and Blood Institute; National Institute on Aging; Cambridge Institute for Medical Research, University of Cambridge; Medical Research Council; Goddard Space Flight Center; National Institutes of Health; Diabetesforeningen; Diabetestutkimussäätiö; H. Lundbeck A/S; Hjartavernd; Institut de Cardiologie de Montréal; Fondation Institut de Cardiologie de Montréal; Paavo Nurmen Säätiö; Svenska Kulturfonden; National Health and Medical Research Council; Oulun Yliopisto; Sydäntutkimussäätiö; National Institute of Mental Health; Göteborgs Läkaresällskap; Technische Universität Dresden; Augustinus Fonden; Vetenskapsrådet; National Institute on Alcohol Abuse and Alcoholism; Stockholms Läns Landsting; GlaxoSmithKline; Signe ja Ane Gyllenbergin Säätiö; Fondation Leenaards; Päivikki ja Sakari Sohlbergin Säätiö; National Institute of Diabetes and Digestive and Kidney Diseases; Norwegian Institute of Public Health; Helsingin ja Uudenmaan Sairaanhoitopiiri; Knut och Alice Wallenbergs Stiftelse; Karolinska Institutet; Juho Vainion Säätiö; British Heart Foundation; Bundesministerium für Bildung und Forschung; Schweizerischer Nationalfonds zur Förderung der Wissenschaftlichen Forschung; Institut National de la Santé et de la Recherche Médicale; AstraZeneca; European Commission; Finska Läkaresällskapet; Yrjö Jahnssonin Säätiö; Cancerfonden; Juvenile Diabetes Research Foundation International; Diabetes UK; Lastentautien Tutkimussäätiö; National Institute for Health and Care Research; Wellcome Trust; Cancer Research UK; Erasmus Medisch Centrum; Stiftelsen för Strategisk Forskning; Healthway; Scottish Government; National Cancer Institute; Lundbeckfonden; Foundation for Cardiovascular Research; National Science Foundation; Fondation Leducq; Centre for Medical Systems Biology; Novo Nordisk; Hjärt-Lungfonden; Agency for Science, Technology and Research; Jalmari ja Rauha Ahokkaan Säätiö; Kela; Svenska Läkaresällskapet; Nederlandse Organisatie voor Wetenschappelijk Onderzoek; Deutsche Forschungsgemeinschaft; Hjerteforeningen; Biomedicum Helsinki-säätiö; Donald W. Reynolds Foundation; Chinese Society of Clinical Oncology; Amgen","keywords":"Biology; Body mass index; Genetics; Genome-wide association study; Single-nucleotide polymorphism; Obesity; Genetic association; Quantitative trait locus; SNP; Gene; Genotype; Endocrinology","score_opus":0.023011521181042795,"score_gpt":0.30459850238047115,"score_spread":0.2815869811994284,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2147311167","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9954556,0.000653247,0.0012128922,0.00009216841,0.000026146929,0.000012222978,0.0014336281,0.000041565196,0.0010725603],"genre_scores_gemma":[0.9945574,0.00026102955,0.002093517,0.00007798913,0.000039786515,0.00003357445,0.0014444904,0.000036971967,0.0014552803],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99910647,0.00019532954,0.00007130227,0.00034760602,0.00016791842,0.00011129648],"domain_scores_gemma":[0.9979006,0.0011330897,0.00043091786,0.00020431014,0.0001256085,0.00020545357],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0009882301,0.0010123666,0.0008940814,0.0015531649,0.0009677325,0.00066487776,0.0007649132,0.0009294217,0.004511566],"category_scores_gemma":[0.0022060385,0.0005771393,0.0008566349,0.0029091074,0.00056335144,0.00020060095,0.0003959385,0.0007971943,0.00077106466],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0028805428,0.00021087135,0.9407631,0.00008563065,0.0012208483,0.001873683,0.00083273364,0.00036397434,0.034779195,0.0004056396,0.0010768926,0.01550698],"study_design_scores_gemma":[0.0000996489,0.0001266242,0.99563247,0.000008226831,0.00035931557,0.0013132505,0.000086102526,0.00028319488,0.0008026829,0.00019159714,0.0010824145,0.000014455374],"about_ca_topic_score_codex":0.0039933138,"about_ca_topic_score_gemma":0.0060375184,"teacher_disagreement_score":0.004511566,"about_ca_system_score_codex":0.00020268506,"about_ca_system_score_gemma":0.0003107909,"threshold_uncertainty_score":0.015092671},"labels":[],"label_agreement":null},{"id":"W2147593372","doi":"10.1038/ng.946","title":"Identification of genetic elements that autonomously determine DNA methylation states","year":2011,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Epigenetics and DNA Methylation","field":"Biochemistry, Genetics and Molecular Biology","cited_by":398,"is_retracted":false,"has_abstract":false,"route_ca_aff":false,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"","funders":"National Institutes of Health; University of British Columbia","keywords":"Biology; DNA methylation; RNA-Directed DNA Methylation; Epigenetics; Methylation; Epigenetics of physical exercise; Genetics; CpG site; Epigenomics; Illumina Methylation Assay; DNA; Molecular biology; Gene; Gene expression","score_opus":0.01686941295586851,"score_gpt":0.27112472175786817,"score_spread":0.25425530880199965,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2147593372","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9502488,0.000885983,0.0407662,0.00036650253,0.00012082974,0.000050642284,0.00062458677,0.0004790631,0.0064573814],"genre_scores_gemma":[0.98045564,0.00029340302,0.013232294,0.000109687426,0.000018126815,0.000028113245,0.0006506104,0.00012811327,0.005084051],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9998319,0.000015934922,0.000009915746,0.00006051524,0.00005443087,0.000027279868],"domain_scores_gemma":[0.9995442,0.00019617622,0.0000716871,0.00008394575,0.000038339003,0.00006553982],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00028697064,0.00022165528,0.00024483106,0.00042479107,0.00024135588,0.0006144089,0.00047276024,0.0004955067,0.001384254],"category_scores_gemma":[0.0006104547,0.00035363983,0.00024247498,0.00014510141,0.00042784066,0.00040265295,0.0005879729,0.0009576387,0.00067985454],"study_design_candidate":"bench_or_experimental","study_design_consensus":"bench_or_experimental","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.000051729454,0.00001341987,0.00034098278,0.000009292676,0.0000019946076,0.000023085493,0.000015861207,0.00006827481,0.9960698,0.0010733545,0.00003146686,0.0023007076],"study_design_scores_gemma":[0.0000120587265,0.000038634473,0.0036970645,0.0000028743343,0.000008595018,0.00012228847,0.000021548196,0.0022349511,0.99107164,0.0006782207,0.0021033152,0.000008737249],"about_ca_topic_score_codex":0.00084618264,"about_ca_topic_score_gemma":0.0020345817,"teacher_disagreement_score":0.001384254,"about_ca_system_score_codex":0.0004181951,"about_ca_system_score_gemma":0.0003031401,"threshold_uncertainty_score":0.004630804},"labels":[],"label_agreement":null},{"id":"W2147843065","doi":"10.1038/ng.748","title":"Tartrate-resistant acid phosphatase deficiency causes a bone dysplasia with autoimmunity and a type I interferon expression signature","year":2011,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Systemic Lupus Erythematosus Research","field":"Medicine","cited_by":259,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"SickKids Foundation; Hospital for Sick Children; University of Toronto","funders":"Biotechnology and Biological Sciences Research Council; Wellcome Trust","keywords":"Autoimmunity; Biology; Tartrate-resistant acid phosphatase; Immunology; Systemic lupus erythematosus; Interferon; Haplotype; Dysplasia; Acid phosphatase; Internal medicine; Genetics; Gene; Disease; Medicine; Genotype; Antibody; Biochemistry","score_opus":0.02248478955177482,"score_gpt":0.2760773909865677,"score_spread":0.2535926014347929,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2147843065","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.994689,0.0006116119,0.0017302731,0.00039824753,0.00005509184,0.000028886809,0.00033690926,0.00010812351,0.0020418705],"genre_scores_gemma":[0.997766,0.00019195846,0.0009438935,0.00011544081,0.000031895102,0.000007580832,0.00016047053,0.000021180242,0.0007615404],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.999652,0.000054153363,0.000050418323,0.00007618408,0.000104212064,0.00006303198],"domain_scores_gemma":[0.9995808,0.000106765845,0.00012391104,0.000034198176,0.00003532913,0.00011903324],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0001597257,0.0007649762,0.00037036632,0.0009404204,0.0003285705,0.00033763176,0.00037029624,0.0010639897,0.0013852806],"category_scores_gemma":[0.00043655947,0.0003198503,0.00051807874,0.00039939754,0.00050178944,0.00018403164,0.00032979724,0.00062182854,0.00036700902],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0008326091,0.000080439415,0.0064660045,0.00006142457,0.000051375628,0.07317524,0.00006261791,0.00014614912,0.9155117,0.00040726765,0.00029635936,0.002908653],"study_design_scores_gemma":[0.000324953,0.0009546297,0.14919992,0.000028105555,0.0003109852,0.4376489,0.00028733796,0.002180188,0.40348354,0.0010138709,0.004515486,0.000052124316],"about_ca_topic_score_codex":0.00077526685,"about_ca_topic_score_gemma":0.00095416204,"teacher_disagreement_score":0.0013852806,"about_ca_system_score_codex":0.00029616372,"about_ca_system_score_gemma":0.00024027629,"threshold_uncertainty_score":0.0046342015},"labels":[],"label_agreement":null},{"id":"W2148512375","doi":"10.1038/ng.668","title":"A genome-wide association study identifies susceptibility loci for ovarian cancer at 2q31 and 8q24","year":2010,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Ovarian cancer diagnosis and treatment","field":"Medicine","cited_by":353,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Women's College Hospital; Alberta Health Services; Cancer Care Ontario; BC Cancer Agency; Simon Fraser University; University of Toronto","funders":"National Cancer Institute; National Institutes of Health; Cancer Research UK; Wellcome Trust","keywords":"Biology; Genome-wide association study; Single-nucleotide polymorphism; Ovarian cancer; Genetics; Locus (genetics); Candidate gene; Genetic association; Cancer; Gene; Genotype","score_opus":0.011487030395675082,"score_gpt":0.30316804794095464,"score_spread":0.2916810175452796,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2148512375","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9977034,0.00052380055,0.0005404105,0.00032586203,0.000027461836,0.000017441977,0.0003359558,0.000027040618,0.0004987239],"genre_scores_gemma":[0.9982414,0.00019250468,0.0005455285,0.0000758486,0.000038851373,0.00001824762,0.00035370226,0.000009799174,0.0005240466],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9995987,0.00011166459,0.00002947695,0.00011246518,0.000092987204,0.000054828663],"domain_scores_gemma":[0.9988226,0.0005288683,0.00029084983,0.000109359695,0.00009105559,0.00015712828],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0006284937,0.0005752921,0.0004908681,0.0014648123,0.0007161294,0.00053232315,0.0006246292,0.00080605864,0.0029543696],"category_scores_gemma":[0.0024272501,0.0003674212,0.00075655937,0.0013075785,0.00044321865,0.00023797152,0.000626167,0.00081482116,0.00022193698],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00655833,0.0004377716,0.83082676,0.00012091384,0.001569295,0.008081409,0.0006221423,0.00051922654,0.12960026,0.00048393357,0.0024279025,0.018751942],"study_design_scores_gemma":[0.00048208243,0.00038903733,0.98638225,0.000017056413,0.00075382343,0.0052926466,0.00016078836,0.00072763965,0.0036105968,0.00045243965,0.0017103497,0.000021230773],"about_ca_topic_score_codex":0.0030335258,"about_ca_topic_score_gemma":0.0049668923,"teacher_disagreement_score":0.0030335258,"about_ca_system_score_codex":0.00022280456,"about_ca_system_score_gemma":0.00034752913,"threshold_uncertainty_score":0.009883344},"labels":[],"label_agreement":null},{"id":"W2148749248","doi":"10.1038/ng.2897","title":"Genome-wide trans-ancestry meta-analysis provides insight into the genetic architecture of type 2 diabetes susceptibility","year":2014,"lang":"en","type":"review","venue":"Nature Genetics","topic":"Genetic Associations and Epidemiology","field":"Biochemistry, Genetics and Molecular Biology","cited_by":1079,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Toronto","funders":"FP7 Health; National Institute of Diabetes and Digestive and Kidney Diseases; Instituto de Seguriidad y Servicios Sociales de los Trabadores del Estado; Medical Research Council; Novo Nordisk Fonden; Instituto Mexicano del Seguro Social; Eunice Kennedy Shriver National Institute of Child Health and Human Development; European Commission; Canadian Institutes of Health Research; National Institute of General Medical Sciences; National Institute for Health and Care Research; National Institutes of Health; National Center for Advancing Translational Sciences; National Human Genome Research Institute; Wellcome Trust; Consejo Nacional de Ciencia y Tecnología; British Heart Foundation","keywords":"Genome-wide association study; Biology; Genetic architecture; Genetics; Genetic association; Single-nucleotide polymorphism; Genetic genealogy; Allele; Type 2 diabetes; 1000 Genomes Project; Meta-analysis; Evolutionary biology; Quantitative trait locus; Gene; Genotype; Diabetes mellitus; Population; Medicine; Environmental health","score_opus":0.0326100269849037,"score_gpt":0.31714584627664566,"score_spread":0.284535819291742,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2148749248","genre_codex":"review","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":null,"domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.00060670293,0.9971826,0.0007848809,0.0008047,0.00015152567,0.0000037480008,0.00017219779,0.000013618686,0.00027998321],"genre_scores_gemma":[0.006701093,0.9902532,0.0013061147,0.00074576406,0.000433236,0.000010799695,0.0002986677,0.000008467898,0.0002427047],"study_design_codex":"design_other","study_design_gemma":"meta_analysis","domain_scores_codex":[0.9992442,0.00025852452,0.00008839414,0.00021500261,0.00015299962,0.0000409877],"domain_scores_gemma":[0.99729025,0.002004561,0.00022646895,0.00011569748,0.00027805252,0.00008500437],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.003099081,0.0011509483,0.0029024028,0.0017760389,0.00017353652,0.0011110631,0.0012613186,0.0011800178,0.0020440358],"category_scores_gemma":[0.0042067836,0.00043788154,0.0018321249,0.0028345413,0.0004526251,0.0007334698,0.00092990353,0.0018432707,0.00048477974],"study_design_candidate":"meta_analysis","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00059725204,0.000041781226,0.011344456,0.017346567,0.0105648,0.00036652194,0.00006612469,0.000752358,0.0011722043,0.0032153032,0.019444188,0.9350885],"study_design_scores_gemma":[0.0006464441,0.00049580657,0.10171533,0.025310988,0.05722013,0.0063862866,0.00034583677,0.0018329729,0.0022401826,0.04090414,0.7625918,0.00031014121],"about_ca_topic_score_codex":0.0025812883,"about_ca_topic_score_gemma":0.006183269,"teacher_disagreement_score":0.003099081,"about_ca_system_score_codex":0.000545193,"about_ca_system_score_gemma":0.001636271,"threshold_uncertainty_score":0.016389728},"labels":[],"label_agreement":null},{"id":"W2148977592","doi":"10.1038/ng.3226","title":"A common variant mapping to CACNA1A is associated with susceptibility to exfoliation syndrome","year":2015,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Genetic Neurodegenerative Diseases","field":"Neuroscience","cited_by":129,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Dalhousie University","funders":"Wellcome Trust; National Eye Institute; Howard Hughes Medical Institute","keywords":"Biology; Genetics; Computational biology; Bioinformatics","score_opus":0.042809054645324085,"score_gpt":0.2881270169217583,"score_spread":0.2453179622764342,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2148977592","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99389523,0.0010412032,0.0016103649,0.0005172698,0.00029726492,0.000058612524,0.00069374376,0.00012011665,0.0017661942],"genre_scores_gemma":[0.9973031,0.00016396644,0.00096363795,0.00013911857,0.00016207072,0.000018463403,0.00028066296,0.000029646957,0.00093936664],"study_design_codex":"case_report","study_design_gemma":"observational","domain_scores_codex":[0.9990395,0.00016556322,0.00018491007,0.0002860796,0.0002093496,0.00011458193],"domain_scores_gemma":[0.99608326,0.0015978541,0.00127993,0.00020624229,0.00026696429,0.0005657836],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.000593677,0.002879031,0.0012999827,0.0043754824,0.0020646476,0.00076072785,0.0018565773,0.0036441893,0.009577904],"category_scores_gemma":[0.0038911023,0.00037316594,0.0014768955,0.002609075,0.0013589866,0.0004984062,0.0009688381,0.0012568651,0.00092867995],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0060135066,0.00079625676,0.168169,0.00071819074,0.0017501928,0.40280843,0.0029318293,0.0015375332,0.3875208,0.003041749,0.0025458708,0.022166546],"study_design_scores_gemma":[0.00090478896,0.0015722314,0.4878912,0.0004665245,0.002187009,0.43665758,0.0013210891,0.0043280157,0.048476204,0.004081797,0.011767784,0.00034583217],"about_ca_topic_score_codex":0.0037623134,"about_ca_topic_score_gemma":0.0028172748,"teacher_disagreement_score":0.009577904,"about_ca_system_score_codex":0.0005225238,"about_ca_system_score_gemma":0.00049505674,"threshold_uncertainty_score":0.03204125},"labels":[],"label_agreement":null},{"id":"W2149076288","doi":"10.1038/ng885","title":"Mutation of GABRA1 in an autosomal dominant form of juvenile myoclonic epilepsy","year":2002,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Neuroscience and Neuropharmacology Research","field":"Neuroscience","cited_by":653,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Montreal General Hospital; McGill University; Centre Hospitalier de l’Université de Montréal; Hôpital Notre-Dame; Centre Hospitalier Universitaire Sainte-Justine; Health Sciences Centre; University of Toronto; McGill University Health Centre; Sunnybrook Health Science Centre; Hospital for Sick Children; University of British Columbia","funders":"","keywords":"Juvenile myoclonic epilepsy; Biology; Epilepsy; Idiopathic generalized epilepsy; Mutation; Receptor; Childhood absence epilepsy; Protein subunit; Mutant; Genetics; Myoclonic epilepsy; Juvenile; Internal medicine; Neuroscience; Gene; Medicine","score_opus":0.03672045109770524,"score_gpt":0.3390598175320563,"score_spread":0.30233936643435105,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2149076288","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99386203,0.0006179035,0.0018310914,0.0007622154,0.00017673559,0.0000543719,0.0002303368,0.0001470063,0.0023183979],"genre_scores_gemma":[0.9978429,0.00012570394,0.00079770375,0.0001394527,0.00006673743,0.000009209963,0.00006856261,0.00003215672,0.0009175636],"study_design_codex":"case_report","study_design_gemma":"observational","domain_scores_codex":[0.99960417,0.00006202504,0.000074183445,0.00007744707,0.000103305945,0.00007883227],"domain_scores_gemma":[0.9989249,0.00040368678,0.00028311033,0.00004469803,0.00009618042,0.00024735226],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00031303035,0.0021222602,0.0008185086,0.0013251486,0.0010663265,0.00046689992,0.00087036076,0.0024631687,0.0021617005],"category_scores_gemma":[0.0015797106,0.00041079117,0.0009756353,0.000592265,0.0011745207,0.00044056677,0.00087657705,0.00097084424,0.00071218703],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0007317866,0.00006512569,0.008016363,0.0000989153,0.00010007136,0.8479934,0.0006460033,0.0006153931,0.13543178,0.00088485616,0.0005631235,0.0048531042],"study_design_scores_gemma":[0.00029339228,0.00068858324,0.06524275,0.00008139249,0.00038851635,0.8717714,0.0007084568,0.0038236936,0.052506216,0.00090191414,0.0034384078,0.00015533416],"about_ca_topic_score_codex":0.0053753336,"about_ca_topic_score_gemma":0.0060485196,"teacher_disagreement_score":0.0053753336,"about_ca_system_score_codex":0.0007245606,"about_ca_system_score_gemma":0.00068127597,"threshold_uncertainty_score":0.0106880665},"labels":[],"label_agreement":null},{"id":"W2149633671","doi":"10.1038/ng.3093","title":"HLA-DQA1–HLA-DRB1 variants confer susceptibility to pancreatitis induced by thiopurine immunosuppressants","year":2014,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Pancreatitis Pathology and Treatment","field":"Medicine","cited_by":191,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Mount Sinai Hospital; University of Alberta","funders":"Crohn's and Colitis UK; Academy of Medical Sciences; National Institute for Health and Care Research; Wellcome Trust","keywords":"Thiopurine methyltransferase; Azathioprine; Mercaptopurine; Odds ratio; Inflammatory bowel disease; Human leukocyte antigen; Autoimmune pancreatitis; Pancreatitis; Biology; Haplotype; Internal medicine; Ulcerative colitis; Genome-wide association study; Immunology; Medicine; Disease; Genotype; Genetics; Single-nucleotide polymorphism","score_opus":0.0103838532072105,"score_gpt":0.2798820751278678,"score_spread":0.26949822192065725,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2149633671","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9991722,0.0001327093,0.0001244612,0.00006321683,0.0000082083225,0.000002940942,0.000032846445,0.0000046980617,0.00045869476],"genre_scores_gemma":[0.99960786,0.00004021339,0.00008402061,0.000018445864,0.000013241961,0.0000013038099,0.00003241944,0.000003686795,0.00019882435],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9995363,0.00020093084,0.000048558853,0.00008098474,0.000047226586,0.000086039596],"domain_scores_gemma":[0.9985393,0.00040987684,0.0005862173,0.00011117498,0.00007825248,0.00027517276],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00045786513,0.00038919793,0.00032934418,0.0006533861,0.00030644782,0.00046017405,0.0002690907,0.00046673056,0.0050190277],"category_scores_gemma":[0.0012916138,0.00023939567,0.00051470194,0.00063393876,0.0002988167,0.00022912235,0.00031549466,0.00067559077,0.00028512214],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.011340115,0.00071339635,0.8171385,0.00007585846,0.00075086765,0.0075099515,0.00037732834,0.00030385196,0.15064457,0.0006145704,0.00039351863,0.010137472],"study_design_scores_gemma":[0.00019373545,0.0013276057,0.97917616,0.000020651718,0.00037977748,0.011239993,0.00021037566,0.0006990862,0.005528452,0.00036152496,0.000845005,0.000017660155],"about_ca_topic_score_codex":0.00060849654,"about_ca_topic_score_gemma":0.00030699963,"teacher_disagreement_score":0.0050190277,"about_ca_system_score_codex":0.00015206797,"about_ca_system_score_gemma":0.00011869388,"threshold_uncertainty_score":0.01679033},"labels":[],"label_agreement":null},{"id":"W2149665587","doi":"10.1038/ng.2261","title":"Meta-analysis identifies six new susceptibility loci for atrial fibrillation","year":2012,"lang":"en","type":"review","venue":"Nature Genetics","topic":"Genetic Associations and Epidemiology","field":"Biochemistry, Genetics and Molecular Biology","cited_by":609,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Ottawa","funders":"National Center for Advancing Translational Sciences; National Institute on Drug Abuse; National Heart, Lung, and Blood Institute","keywords":"Genome-wide association study; Atrial fibrillation; Biology; Candidate gene; Stroke (engine); Genetic association; Genetics; Internal medicine; Gene; Bioinformatics; Single-nucleotide polymorphism; Genotype; Medicine","score_opus":0.09848053616384907,"score_gpt":0.38174439206564337,"score_spread":0.2832638559017943,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2149665587","genre_codex":"review","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":null,"domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.002605586,0.9934186,0.0018613109,0.0010637722,0.00024419161,0.000008593142,0.00026026805,0.000025274143,0.0005123831],"genre_scores_gemma":[0.031396728,0.9617378,0.0036473013,0.0011396224,0.0010631991,0.000032205666,0.0005979615,0.000014190934,0.00037097104],"study_design_codex":"design_other","study_design_gemma":"meta_analysis","domain_scores_codex":[0.9992142,0.00024265888,0.0001298639,0.00020287771,0.0001707421,0.00003970503],"domain_scores_gemma":[0.9965198,0.0027369226,0.0003184201,0.0001341052,0.00022285598,0.00006792725],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0027868515,0.0014097213,0.0032360265,0.0016545651,0.00014495841,0.0012819024,0.0011771825,0.0013340807,0.0018179647],"category_scores_gemma":[0.004799472,0.00044490065,0.0028532585,0.00239847,0.00033969228,0.0006291377,0.00058334187,0.0014189099,0.00032411743],"study_design_candidate":"meta_analysis","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.001957925,0.00009549087,0.037850324,0.028850345,0.047677346,0.0011857513,0.00008328084,0.0015357087,0.0023111084,0.0034037754,0.022010237,0.85303867],"study_design_scores_gemma":[0.002662862,0.0011933201,0.22176237,0.023352431,0.3015028,0.013309396,0.00040498894,0.0037763398,0.0049910764,0.042630177,0.38396373,0.00045047182],"about_ca_topic_score_codex":0.0013674834,"about_ca_topic_score_gemma":0.0040797982,"teacher_disagreement_score":0.0032360265,"about_ca_system_score_codex":0.00043385767,"about_ca_system_score_gemma":0.0011011552,"threshold_uncertainty_score":0.0147384405},"labels":[],"label_agreement":null},{"id":"W2149813409","doi":"10.1038/ng.628","title":"Excess of rare variants in genes identified by genome-wide association study of hypertriglyceridemia","year":2010,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Lipid metabolism and disorders","field":"Medicine","cited_by":444,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Hamilton Health Sciences; McMaster University; Population Health Research Institute; Western University","funders":"National Center for Research Resources; National Heart, Lung, and Blood Institute; Canadian Institutes of Health Research; National Institutes of Health","keywords":"Genome-wide association study; Biology; Genetics; Genetic association; Missense mutation; Gene; Phenotype; Quantitative trait locus; Hypertriglyceridemia; Single-nucleotide polymorphism; Genotype; Cholesterol; Endocrinology","score_opus":0.007257673477195975,"score_gpt":0.2656347536626905,"score_spread":0.25837708018549455,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2149813409","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9943151,0.0021030463,0.001350122,0.00028825973,0.00011063985,0.000008895916,0.0005959194,0.00008536207,0.0011427023],"genre_scores_gemma":[0.9984384,0.00024040558,0.00042313038,0.000104531595,0.00012769294,0.000004976718,0.00031410795,0.000023954108,0.00032280214],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99766976,0.000669635,0.00036216082,0.0006785929,0.0004399331,0.0001799196],"domain_scores_gemma":[0.993576,0.0033409891,0.0013297625,0.00080845226,0.00038858,0.0005562214],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0014461406,0.00078418496,0.0009921961,0.0031419606,0.00089875114,0.0010770316,0.00096694764,0.0017810549,0.005155843],"category_scores_gemma":[0.0054200552,0.00049359555,0.0011456972,0.0019358202,0.00085462077,0.0005255059,0.0006360424,0.0011197659,0.00067057763],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.009463907,0.00028178404,0.7759542,0.0002941971,0.0036189985,0.012486837,0.0004346119,0.0007157793,0.17777078,0.0012225301,0.0013143832,0.016442096],"study_design_scores_gemma":[0.00028571207,0.00039186966,0.96975046,0.000051456016,0.0024735543,0.01738209,0.00018169644,0.0013817735,0.005457237,0.0012032897,0.0013966114,0.000044220335],"about_ca_topic_score_codex":0.0013046471,"about_ca_topic_score_gemma":0.0012496148,"teacher_disagreement_score":0.005155843,"about_ca_system_score_codex":0.0001584054,"about_ca_system_score_gemma":0.00020869376,"threshold_uncertainty_score":0.017247975},"labels":[],"label_agreement":null},{"id":"W2150170782","doi":"10.1038/ng.465","title":"SOX2 is an amplified lineage-survival oncogene in lung and esophageal squamous cell carcinomas","year":2009,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Epigenetics and DNA Methylation","field":"Biochemistry, Genetics and Molecular Biology","cited_by":952,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Princess Margaret Cancer Centre; University Health Network","funders":"National Institute of General Medical Sciences; National Cancer Institute; National Institutes of Health","keywords":"Biology; Cancer research; SOX2; Ectopic expression; Esophagus; Oncogene; Cellular differentiation; Transcription factor; Cell; Cell culture; Gene; Genetics; Cell cycle","score_opus":0.010171743424887641,"score_gpt":0.27444935615281735,"score_spread":0.2642776127279297,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2150170782","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99692744,0.0007760239,0.00067133975,0.000044630226,0.000009533275,0.0000068113186,0.00012671323,0.000020993288,0.0014165823],"genre_scores_gemma":[0.99761873,0.00024739993,0.00027954738,0.000009924473,0.000007084697,0.000004948619,0.0001959384,0.000006795389,0.0016296186],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99987304,0.000017717339,0.000013401045,0.000018132409,0.000052031162,0.000025682997],"domain_scores_gemma":[0.9998292,0.00003706621,0.000030363404,0.000018908237,0.000030484745,0.000053961372],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00022470993,0.00018775249,0.00019266458,0.0006232353,0.00022547676,0.00037245548,0.00016874542,0.00018951348,0.0017707556],"category_scores_gemma":[0.00027848993,0.00020366258,0.00014598599,0.0003321993,0.00026032265,0.00021379905,0.00025240658,0.00020114872,0.00027173018],"study_design_candidate":"bench_or_experimental","study_design_consensus":"bench_or_experimental","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00048174552,0.000020650228,0.023044033,0.000034555425,0.000021922868,0.0011258333,0.00007883187,0.000086192165,0.9719059,0.0003508044,0.00009110222,0.0027585032],"study_design_scores_gemma":[0.000068799745,0.00022885272,0.42022353,0.000012546941,0.000101061785,0.008213668,0.00047744604,0.0019758295,0.5634789,0.00051197526,0.0046931272,0.0000142454255],"about_ca_topic_score_codex":0.0015097543,"about_ca_topic_score_gemma":0.0020367817,"teacher_disagreement_score":0.0017707556,"about_ca_system_score_codex":0.00025861867,"about_ca_system_score_gemma":0.0002107313,"threshold_uncertainty_score":0.0059238076},"labels":[],"label_agreement":null},{"id":"W2150600032","doi":"10.1038/ng.2656","title":"Mycobacterium tuberculosis mutation rate estimates from different lineages predict substantial differences in the emergence of drug-resistant tuberculosis","year":2013,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Tuberculosis Research and Epidemiology","field":"Medicine","cited_by":482,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of British Columbia; BC Centre for Disease Control","funders":"National Institute of Allergy and Infectious Diseases; National Institute of General Medical Sciences; National Institutes of Health; National Center for Chronic Disease Prevention and Health Promotion; Howard Hughes Medical Institute","keywords":"Tuberculosis; Mycobacterium tuberculosis; Biology; Mutation rate; Lineage (genetic); Drug resistance; Mutation; Antibiotics; Microbiology; Genetics; Virology; Gene; Medicine; Pathology","score_opus":0.01631119637757917,"score_gpt":0.29183782800613645,"score_spread":0.2755266316285573,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2150600032","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9976037,0.00031322107,0.0014330162,0.000051360355,0.000005933849,0.0000040940567,0.00016212142,0.00001537458,0.00041119076],"genre_scores_gemma":[0.9992205,0.00005671865,0.00047393213,0.000039868934,0.0000042807337,0.0000016014204,0.00015810737,0.000011350709,0.00003354459],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9985195,0.00064921536,0.00012940272,0.00036687346,0.00018711686,0.00014790859],"domain_scores_gemma":[0.99237,0.004344148,0.0016572434,0.0007869995,0.00056609,0.00027555868],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0030411077,0.00045263936,0.00045956144,0.0011701359,0.0003552137,0.0012441865,0.00058448775,0.0012025916,0.0010501607],"category_scores_gemma":[0.009488662,0.0004244739,0.00051058776,0.000724737,0.00045340715,0.0006948787,0.0005497178,0.00116324,0.00048245132],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0007090596,0.00006500318,0.92449504,0.000044719083,0.0003795784,0.00017172504,0.00044441377,0.0027187008,0.059551343,0.0005146725,0.00019110525,0.01071476],"study_design_scores_gemma":[0.000033731074,0.00017076277,0.97703207,0.0000300894,0.00015255499,0.00077457045,0.00034801944,0.01180754,0.007972534,0.0011218826,0.00052508316,0.00003115223],"about_ca_topic_score_codex":0.00089546596,"about_ca_topic_score_gemma":0.0013391318,"teacher_disagreement_score":0.0030411077,"about_ca_system_score_codex":0.00030297917,"about_ca_system_score_gemma":0.00011943674,"threshold_uncertainty_score":0.016083062},"labels":[],"label_agreement":null},{"id":"W2150806217","doi":"10.1038/ng.685","title":"Meta-analysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distribution","year":2010,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Genetic Associations and Epidemiology","field":"Biochemistry, Genetics and Molecular Biology","cited_by":962,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"McMaster University; Université de Montréal; Montreal Heart Institute","funders":"National Center for Research Resources; National Institute of Diabetes and Digestive and Kidney Diseases; National Institute on Aging; National Heart, Lung, and Blood Institute; National Institute of Mental Health; Medical Research Council; U.S. Public Health Service; National Institutes of Health; Schweizerischer Nationalfonds zur Förderung der Wissenschaftlichen Forschung; National Institute of General Medical Sciences; National Institute for Health and Care Research; National Human Genome Research Institute; Wellcome Trust; Nederlandse Organisatie voor Wetenschappelijk Onderzoek; National Cancer Institute; British Heart Foundation","keywords":"Biology; Sexual dimorphism; Waist–hip ratio; Trait; Body fat percentage; Body mass index; Genetics; Quantitative trait locus; Genome-wide association study; Anthropometry; Meta-analysis; Waist; Internal medicine; Gene; Single-nucleotide polymorphism; Genotype; Endocrinology; Medicine","score_opus":0.022452908491160137,"score_gpt":0.27424931367971334,"score_spread":0.2517964051885532,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2150806217","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9501982,0.033392966,0.010975623,0.001075307,0.0002730625,0.000042116153,0.0027351168,0.00023138715,0.0010762365],"genre_scores_gemma":[0.99247664,0.0035729972,0.0024139762,0.00018505668,0.00010724047,0.00002804801,0.0008331678,0.00006106766,0.00032190172],"study_design_codex":"observational","study_design_gemma":"meta_analysis","domain_scores_codex":[0.99501556,0.0018924935,0.00055479084,0.0015616475,0.00064559357,0.00032986584],"domain_scores_gemma":[0.99009573,0.0066511887,0.0011969644,0.0012602385,0.00037499773,0.00042096098],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0053543085,0.0020806894,0.0032842983,0.003737074,0.00078732264,0.002114381,0.0014268741,0.0015176444,0.002234609],"category_scores_gemma":[0.008757185,0.0010055073,0.008023888,0.0058246106,0.00070590153,0.0006447183,0.0011873732,0.0015096781,0.00023850008],"study_design_candidate":"meta_analysis","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.003246489,0.00008021998,0.84344566,0.0005429496,0.12688915,0.0012761769,0.0001816608,0.0011645427,0.007846134,0.0003687931,0.0006728181,0.014285342],"study_design_scores_gemma":[0.00043106417,0.00048094598,0.89435315,0.0001384377,0.09601147,0.0017783915,0.00020311157,0.0025435623,0.0017168793,0.0011625963,0.0011162617,0.000064046006],"about_ca_topic_score_codex":0.004485963,"about_ca_topic_score_gemma":0.0068501104,"teacher_disagreement_score":0.0053543085,"about_ca_system_score_codex":0.0003866599,"about_ca_system_score_gemma":0.00069129514,"threshold_uncertainty_score":0.028316677},"labels":[],"label_agreement":null},{"id":"W2151554216","doi":"10.1038/ng.2645","title":"Genome-wide association study identifies two susceptibility loci for osteosarcoma","year":2013,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Genomics and Chromatin Dynamics","field":"Biochemistry, Genetics and Molecular Biology","cited_by":202,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Lunenfeld-Tanenbaum Research Institute; University of Toronto; Mount Sinai Hospital","funders":"National Cancer Institute; National Institutes of Health","keywords":"Osteosarcoma; Biology; Locus (genetics); Genome-wide association study; Genetics; Malignancy; Gene; Genetic association; Single-nucleotide polymorphism; Genotype; Bioinformatics; Cancer research","score_opus":0.0050924666648950396,"score_gpt":0.24871859786775644,"score_spread":0.2436261312028614,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2151554216","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99866915,0.00024827194,0.0005137615,0.0000985266,0.000010998351,0.0000040641544,0.00012120944,0.000015062383,0.00031894745],"genre_scores_gemma":[0.99921703,0.00007401709,0.00027528073,0.000020473786,0.00001102958,0.0000035811152,0.00012206066,0.0000066629223,0.00026983384],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99940085,0.0001640766,0.000067327084,0.0001720274,0.0001081845,0.00008750393],"domain_scores_gemma":[0.99842864,0.0006077674,0.00040759682,0.00014360624,0.00010488656,0.00030741797],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00065687846,0.00054395787,0.00044627773,0.002042377,0.0006928404,0.0005314549,0.00054562493,0.0008322928,0.0026141729],"category_scores_gemma":[0.0012535212,0.0004893704,0.0007817117,0.001519689,0.0006185542,0.00024106173,0.000655205,0.00088408816,0.00027692408],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0043395534,0.00047771566,0.8259015,0.000071154245,0.0007275397,0.0029255066,0.00043622564,0.00020879674,0.15769155,0.00053454645,0.00037206413,0.0063138655],"study_design_scores_gemma":[0.000121714555,0.00030350027,0.9909888,0.000006562987,0.00043131397,0.0025199214,0.00022188848,0.00044531227,0.0041865185,0.00032556264,0.00043320158,0.000015761829],"about_ca_topic_score_codex":0.0016038875,"about_ca_topic_score_gemma":0.0023220442,"teacher_disagreement_score":0.0026141729,"about_ca_system_score_codex":0.00019728977,"about_ca_system_score_gemma":0.00031050807,"threshold_uncertainty_score":0.008745253},"labels":[],"label_agreement":null},{"id":"W2151566815","doi":"10.1038/ng1985","title":"Mapping autism risk loci using genetic linkage and chromosomal rearrangements","year":2007,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Autism Spectrum Disorder Research","field":"Neuroscience","cited_by":1416,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"McGill University; Centre for Addiction and Mental Health; Montreal Children's Hospital; Izaak Walton Killam Health Centre; Hospital for Sick Children; McMaster University","funders":"Eunice Kennedy Shriver National Institute of Child Health and Human Development; National Center for Research Resources; National Institute of Child Health and Human Development; National Institute of Neurological Disorders and Stroke; Canadian Institutes of Health Research; University of California, San Francisco; Assistance publique-Hôpitaux de Paris; Fondation pour la Recherche Médicale; National Institute of Mental Health; Hospital for Sick Children; Centre National de la Recherche Scientifique; Sundhed og Sygdom, Det Frie Forskningsråd; Fondation de France; Deutsche Forschungsgemeinschaft; Ontario Genomics Institute; Orange; Institut National de la Santé et de la Recherche Médicale; University of South Carolina; National Institutes of Health; Ontario Genomics; Genome Canada; Medical Research Council; Howard Hughes Medical Institute; Autism Speaks; University of Miami; Wellcome Trust; Vanderbilt University","keywords":"Biology; Genetics; Copy-number variation; Autism; Genetic architecture; Linkage (software); Heritability of autism; Genetic linkage; SNP; Chromosome; Gene; Candidate gene; Synaptogenesis; Genetic variation; Single-nucleotide polymorphism; Quantitative trait locus; Genome; Phenotype; Genotype; Neuroscience","score_opus":0.025921924552661246,"score_gpt":0.31067310585474633,"score_spread":0.2847511813020851,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2151566815","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.94449425,0.0016086217,0.041685726,0.00066244806,0.00007526344,0.00017486227,0.0010071807,0.00023840238,0.0100532295],"genre_scores_gemma":[0.9525615,0.0016552197,0.040923156,0.00014149415,0.000044560576,0.00021653692,0.0011379023,0.00009799313,0.0032217207],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9991297,0.00021560666,0.000055603356,0.0002697048,0.00020710916,0.0001222956],"domain_scores_gemma":[0.99899167,0.00059696066,0.00021011944,0.00009452309,0.000039253737,0.00006747876],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00082479016,0.00091200264,0.0006813292,0.005662644,0.001045332,0.0008368041,0.0012494338,0.00096268795,0.0064741084],"category_scores_gemma":[0.002005906,0.00068511645,0.0010913513,0.002231461,0.0010348615,0.0005790587,0.001732002,0.0013195776,0.00067214976],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0018925801,0.000586559,0.047913086,0.000298787,0.00065615796,0.0069224,0.0010115682,0.007814367,0.8296708,0.022277659,0.0010990177,0.07985709],"study_design_scores_gemma":[0.0017914313,0.0020990223,0.44711468,0.00037326003,0.0025612535,0.041744612,0.002546487,0.024136124,0.3973032,0.040012598,0.039892994,0.00042442535],"about_ca_topic_score_codex":0.0042672884,"about_ca_topic_score_gemma":0.0065460964,"teacher_disagreement_score":0.0064741084,"about_ca_system_score_codex":0.0006584913,"about_ca_system_score_gemma":0.00050453836,"threshold_uncertainty_score":0.021658063},"labels":[],"label_agreement":null},{"id":"W2151645052","doi":"10.1038/ng.2754","title":"A recurrent germline PAX5 mutation confers susceptibility to pre-B cell acute lymphoblastic leukemia","year":2013,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Acute Lymphoblastic Leukemia research","field":"Medicine","cited_by":329,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of British Columbia","funders":"National Institute of Diabetes and Digestive and Kidney Diseases; National Health and Medical Research Council; KWF Kankerbestrijding; National Cancer Institute; National Institutes of Health; Canadian Institutes of Health Research; Geoffrey Beene Cancer Research Center; American Lebanese Syrian Associated Charities; National Institute of General Medical Sciences; Medical Research Council; Deutsche Forschungsgemeinschaft; St. Jude Children's Research Hospital","keywords":"Biology; PAX5; Loss of heterozygosity; Germline; Germline mutation; Genetics; Mutation; Allele; Molecular biology; B cell; Somatic cell; Cancer research; Gene; Transcription factor; Antibody","score_opus":0.009473553381522998,"score_gpt":0.2931197454918782,"score_spread":0.2836461921103552,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2151645052","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99838006,0.00006542404,0.00022917222,0.00006305921,0.000007673157,0.000006648338,0.000084394786,0.00002777185,0.0011358076],"genre_scores_gemma":[0.99950004,0.000027673093,0.00012828264,0.000016801236,0.0000063443645,0.0000017840334,0.00005147978,0.0000065396225,0.00026102734],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.99977463,0.00005380391,0.00002598467,0.000040037015,0.000051411684,0.00005422802],"domain_scores_gemma":[0.99962926,0.00014323885,0.000083681196,0.00003400661,0.000013160674,0.00009677055],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00015856832,0.00036307503,0.00023426893,0.0009380534,0.0003964686,0.0003214059,0.00035681974,0.00061689515,0.005443414],"category_scores_gemma":[0.00054331194,0.00019656726,0.0003174422,0.0005840623,0.00038710007,0.00015398924,0.0004246631,0.00043219622,0.00046215314],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0017111173,0.0002949802,0.11145064,0.00007676466,0.00013715224,0.083026215,0.00061732635,0.000693759,0.78673136,0.0023410919,0.0006721662,0.012247507],"study_design_scores_gemma":[0.00026611253,0.0021625916,0.5585667,0.000055880206,0.000364177,0.31833044,0.0010099467,0.0041489555,0.105464175,0.0015644083,0.007982805,0.00008376086],"about_ca_topic_score_codex":0.0011226161,"about_ca_topic_score_gemma":0.0011869051,"teacher_disagreement_score":0.005443414,"about_ca_system_score_codex":0.0002701145,"about_ca_system_score_gemma":0.00020061605,"threshold_uncertainty_score":0.018210053},"labels":[],"label_agreement":null},{"id":"W2152381343","doi":"10.1038/ng1885","title":"A high-resolution HLA and SNP haplotype map for disease association studies in the extended human MHC","year":2006,"lang":"en","type":"article","venue":"Nature Genetics","topic":"T-cell and B-cell Immunology","field":"Immunology and Microbiology","cited_by":776,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Université de Montréal; Montreal Heart Institute","funders":"National Institute of Allergy and Infectious Diseases; National Cancer Institute; National Institutes of Health; Wellcome Trust","keywords":"Linkage disequilibrium; Biology; Major histocompatibility complex; Human leukocyte antigen; Genetics; Haplotype; Single-nucleotide polymorphism; Tag SNP; SNP; Genetic association; Balancing selection; MHC class I; Gene; Allele; Genotype; Antigen","score_opus":0.019009240611046283,"score_gpt":0.2829602442684713,"score_spread":0.26395100365742497,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2152381343","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.8213291,0.0037685537,0.1411589,0.00091586687,0.00016315083,0.00036465045,0.021492979,0.0007429389,0.010063906],"genre_scores_gemma":[0.8141309,0.0016602613,0.16014268,0.00035104316,0.00014989916,0.0003047565,0.020103512,0.00017744541,0.002979516],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9997899,0.000057357545,0.000012076379,0.00007478751,0.000039479088,0.0000264731],"domain_scores_gemma":[0.9992435,0.00038681054,0.00005983456,0.000116757656,0.00008260973,0.000110459],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00060408725,0.00023013778,0.0007051431,0.0013539768,0.00060809363,0.0005488817,0.00044011555,0.0003453697,0.0050160782],"category_scores_gemma":[0.0011894124,0.00042042628,0.00048146406,0.0015862974,0.00017961358,0.00022852911,0.0005279706,0.0009883012,0.0011950566],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.002874961,0.0005234744,0.041790403,0.00086611416,0.0006325351,0.0043169144,0.0010705976,0.0125469975,0.6787517,0.0067116455,0.010962809,0.2389519],"study_design_scores_gemma":[0.0016110535,0.0009919736,0.74099076,0.0004394964,0.0015952092,0.0069807908,0.0006595427,0.027140446,0.05097957,0.022780579,0.14559974,0.00023078365],"about_ca_topic_score_codex":0.0019563874,"about_ca_topic_score_gemma":0.004876785,"teacher_disagreement_score":0.0050160782,"about_ca_system_score_codex":0.00019816493,"about_ca_system_score_gemma":0.00043161568,"threshold_uncertainty_score":0.016780496},"labels":[],"label_agreement":null},{"id":"W2152406028","doi":"10.1038/ng.2416","title":"Breast cancer risk–associated SNPs modulate the affinity of chromatin for FOXA1 and alter gene expression","year":2012,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Epigenetics and DNA Methylation","field":"Biochemistry, Genetics and Molecular Biology","cited_by":377,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Princess Margaret Cancer Centre; University of Toronto; University Health Network","funders":"U.S. National Library of Medicine; National Institute of Diabetes and Digestive and Kidney Diseases; National Cancer Institute","keywords":"Single-nucleotide polymorphism; Biology; FOXA1; Genome-wide association study; Epigenomics; Genetics; Breast cancer; Locus (genetics); Chromatin; Epigenome; Imputation (statistics); SNP; 1000 Genomes Project; Gene; Genotype; Cancer; DNA methylation; Gene expression","score_opus":0.008287996979253618,"score_gpt":0.2735177124095517,"score_spread":0.26522971543029805,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2152406028","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.996452,0.0005537916,0.0016098266,0.000180557,0.000026113212,0.0000042566935,0.00028369788,0.000049496408,0.0008402028],"genre_scores_gemma":[0.9986828,0.000097137236,0.0004610526,0.00006059893,0.000007661529,0.000004585033,0.00009179821,0.000016445147,0.00057787384],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.99974364,0.00006488069,0.000014360454,0.000077093886,0.000049962695,0.000050164563],"domain_scores_gemma":[0.9996172,0.00015723723,0.000107604166,0.000048949038,0.000023554576,0.000045369605],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00035384047,0.00022359389,0.00024964445,0.0004018557,0.00018180895,0.00026022614,0.0002552711,0.0003671241,0.0035755017],"category_scores_gemma":[0.00062583236,0.00029031996,0.0002709068,0.00029002424,0.00025442865,0.00013477643,0.00024613098,0.0003778954,0.00036547973],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.001185404,0.00006892447,0.08643597,0.0000596495,0.0003330925,0.00021160174,0.00014366848,0.0005134959,0.9026594,0.0011411858,0.00037922058,0.0068683797],"study_design_scores_gemma":[0.000100596946,0.00026821057,0.79673064,0.000020871808,0.0003027812,0.0009869691,0.00013849544,0.004158431,0.19264123,0.0014179795,0.003204738,0.0000290943],"about_ca_topic_score_codex":0.0018219427,"about_ca_topic_score_gemma":0.003330929,"teacher_disagreement_score":0.0035755017,"about_ca_system_score_codex":0.00023689578,"about_ca_system_score_gemma":0.00011080669,"threshold_uncertainty_score":0.011961281},"labels":[],"label_agreement":null},{"id":"W2152477540","doi":"10.1038/ng.3319","title":"Mutations in the unfolded protein response regulator ATF6 cause the cone dysfunction disorder achromatopsia","year":2015,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Retinal Development and Disorders","field":"Biochemistry, Genetics and Molecular Biology","cited_by":216,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"McGill University Health Centre; SickKids Foundation; Izaak Walton Killam Health Centre; Hospital for Sick Children; University of Toronto","funders":"National Institute of Neurological Disorders and Stroke; National Cancer Institute; Wellcome Trust; National Eye Institute; National Institute of Diabetes and Digestive and Kidney Diseases; National Heart, Lung, and Blood Institute; National Institute for Health and Care Research; U.S. Department of Veterans Affairs","keywords":"Achromatopsia; Biology; Unfolded protein response; Genetics; Brachydactyly; Retinal degeneration; Retinal Disorder; Photophobia; Phenotype; ATF6; Exome sequencing; Retinal; Cell biology; Gene; Neuroscience; Endocrinology","score_opus":0.01042103095439436,"score_gpt":0.25866642271293616,"score_spread":0.2482453917585418,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2152477540","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99584574,0.00041271828,0.0013756482,0.00022643656,0.00007636549,0.000015733785,0.0002496027,0.00011961229,0.0016783016],"genre_scores_gemma":[0.9983829,0.00014777645,0.00065489655,0.000060199643,0.000026011603,0.0000022949064,0.000098502496,0.000024920799,0.0006024577],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99974686,0.000033574837,0.000039780298,0.00005215953,0.00009309488,0.000034489025],"domain_scores_gemma":[0.99963856,0.000092792216,0.000116337906,0.00002206313,0.000035427398,0.00009487348],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00015794583,0.0011108271,0.00046088942,0.0008700039,0.0004912901,0.00032836068,0.0003360917,0.0011176957,0.0013281616],"category_scores_gemma":[0.00055408524,0.0002694008,0.00049939315,0.0005081553,0.0005625236,0.0002559037,0.00050403556,0.00065356825,0.00043736128],"study_design_candidate":"bench_or_experimental","study_design_consensus":"bench_or_experimental","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0015691435,0.00022085923,0.023452057,0.00015769564,0.0002312048,0.19156341,0.0004417722,0.0013723104,0.76685315,0.0017767632,0.0013961843,0.010965483],"study_design_scores_gemma":[0.00038851378,0.0008829677,0.21611257,0.00010192845,0.00060162396,0.48976758,0.0008038347,0.0086104395,0.27124366,0.0028761001,0.008442312,0.00016848069],"about_ca_topic_score_codex":0.0016204934,"about_ca_topic_score_gemma":0.0020959985,"teacher_disagreement_score":0.0016204934,"about_ca_system_score_codex":0.0004068016,"about_ca_system_score_gemma":0.00025437094,"threshold_uncertainty_score":0.0044431686},"labels":[],"label_agreement":null},{"id":"W2153134824","doi":"10.1038/ng1948","title":"Systematic pathway analysis using high-resolution fitness profiling of combinatorial gene deletions","year":2007,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Evolution and Genetic Dynamics","field":"Biochemistry, Genetics and Molecular Biology","cited_by":321,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Toronto","funders":"National Human Genome Research Institute; National Institutes of Health","keywords":"Biology; Genetics; Homologous recombination; Helicase; Gene; Mutant; Computational biology; DNA; Saccharomyces cerevisiae","score_opus":0.006341531402954818,"score_gpt":0.2595607234684978,"score_spread":0.253219192065543,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2153134824","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9502621,0.0005258017,0.04556829,0.00008720918,0.000019033423,0.00008784531,0.0020854797,0.00052374805,0.0008405328],"genre_scores_gemma":[0.9551575,0.0007570768,0.04085956,0.000056175864,0.00000374997,0.00011427856,0.0019598603,0.00019980606,0.0008919078],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.999731,0.000031694977,0.00002591978,0.00007582601,0.00009610779,0.000039485458],"domain_scores_gemma":[0.9994228,0.0001768365,0.0001535909,0.000118960634,0.00006242905,0.000065450164],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00029679743,0.0006645204,0.00055198174,0.0008421262,0.0003237237,0.0007134696,0.00052507134,0.00032023783,0.0006725422],"category_scores_gemma":[0.00044385265,0.00029151622,0.0005952771,0.0007861171,0.00033787102,0.00032955682,0.00063692953,0.0012521723,0.0002590456],"study_design_candidate":"bench_or_experimental","study_design_consensus":"bench_or_experimental","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.000058336307,0.000024035195,0.00060394435,0.00003297753,0.000015572254,0.000032304946,0.000009085007,0.0011015307,0.9951859,0.00022292686,0.000021021347,0.002692369],"study_design_scores_gemma":[0.000015065149,0.00011078747,0.009543422,0.0000064809165,0.00004876525,0.00022350784,0.000036232588,0.021442935,0.96702296,0.00044395088,0.0010845355,0.000021333683],"about_ca_topic_score_codex":0.0010358958,"about_ca_topic_score_gemma":0.0023164635,"teacher_disagreement_score":0.0010358958,"about_ca_system_score_codex":0.0006398677,"about_ca_system_score_gemma":0.00040991802,"threshold_uncertainty_score":0.004642606},"labels":[],"label_agreement":null},{"id":"W2153171441","doi":"10.1038/ng.277","title":"A variant near MTNR1B is associated with increased fasting plasma glucose levels and type 2 diabetes risk","year":2008,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Diet, Metabolism, and Disease","field":"Medicine","cited_by":610,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"McGill University and Génome Québec Innovation Centre; McGill University; Bell (Canada)","funders":"","keywords":"Internal medicine; Endocrinology; Type 2 diabetes; Biology; Diabetes mellitus; Odds ratio; Glucose homeostasis; Pancreatic islets; Circadian rhythm; Insulin resistance; Medicine; Islet","score_opus":0.012260142562353981,"score_gpt":0.23576923138006692,"score_spread":0.22350908881771295,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2153171441","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9956464,0.00086904195,0.0011458589,0.000553616,0.00021264631,0.000021150916,0.00033824556,0.00006732467,0.0011456507],"genre_scores_gemma":[0.9977785,0.00012435149,0.00087677385,0.00018608554,0.00012221608,0.000009756323,0.00014818527,0.000037893104,0.00071613176],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9992151,0.0002664733,0.0001165143,0.00022283944,0.00011615862,0.00006289625],"domain_scores_gemma":[0.9975278,0.00081914314,0.0008983718,0.00012993002,0.00015884449,0.0004658607],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0006762868,0.0012793897,0.0008534702,0.0011874473,0.001253732,0.00070091686,0.0008116942,0.0025120787,0.0059656114],"category_scores_gemma":[0.0025583557,0.00043871943,0.00082045456,0.0011426889,0.0007224642,0.0003358118,0.00038332722,0.0011823975,0.0009350281],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.037102133,0.0017906275,0.44064146,0.0005932733,0.003527347,0.08524074,0.0014290519,0.0019121369,0.39500502,0.002533827,0.004755341,0.02546913],"study_design_scores_gemma":[0.0024351417,0.002979454,0.84715223,0.00038017012,0.001976766,0.11100725,0.00069802324,0.006398684,0.016646512,0.0037420634,0.0063285353,0.00025514167],"about_ca_topic_score_codex":0.0025708214,"about_ca_topic_score_gemma":0.0019491183,"teacher_disagreement_score":0.0059656114,"about_ca_system_score_codex":0.00029689397,"about_ca_system_score_gemma":0.00020841102,"threshold_uncertainty_score":0.019957006},"labels":[],"label_agreement":null},{"id":"W2153968413","doi":"10.1038/ng.2232","title":"Bayesian inference analyses of the polygenic architecture of rheumatoid arthritis","year":2012,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Genetic Associations and Epidemiology","field":"Biochemistry, Genetics and Molecular Biology","cited_by":413,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Mount Sinai Hospital; University of Toronto; University Health Network","funders":"National Institute of Arthritis and Musculoskeletal and Skin Diseases; National Institute of General Medical Sciences; Canadian Institutes of Health Research; National Institutes of Health; Burroughs Wellcome Fund; Biogen; Canada Research Chairs; Wellcome Trust","keywords":"Genome-wide association study; Biology; Genetic architecture; Single-nucleotide polymorphism; Rheumatoid arthritis; Genetics; Quantitative trait locus; Immunology; Gene; Genotype","score_opus":0.012194022052332006,"score_gpt":0.30114090968739315,"score_spread":0.28894688763506116,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2153968413","genre_codex":"methods","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":null,"domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.2783116,0.0024203947,0.7134928,0.0020952015,0.00007203069,0.00009868723,0.0011081343,0.000487673,0.001913518],"genre_scores_gemma":[0.89822966,0.0010438368,0.095788285,0.0004463366,0.00021891278,0.00014779008,0.0015473955,0.00015698542,0.0024209262],"study_design_codex":"simulation_or_modeling","study_design_gemma":"simulation_or_modeling","domain_scores_codex":[0.99089456,0.007021229,0.00033098963,0.0009436177,0.00048452758,0.00032508708],"domain_scores_gemma":[0.8769673,0.115779296,0.0023470973,0.0031965636,0.0010303078,0.0006795273],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.02256564,0.0009365228,0.001960089,0.002910304,0.0015676559,0.0022424103,0.003089661,0.0016644107,0.003568374],"category_scores_gemma":[0.077974774,0.001503127,0.00259448,0.0020481024,0.0018262446,0.0022410718,0.0020345952,0.0038592918,0.00039831956],"study_design_candidate":"simulation_or_modeling","study_design_consensus":"simulation_or_modeling","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0017964774,0.00038051794,0.06951478,0.00040076594,0.003655079,0.0007042538,0.001035581,0.6255928,0.0036101162,0.17589778,0.0040159617,0.11339591],"study_design_scores_gemma":[0.0002230639,0.00006936336,0.012925032,0.00005987593,0.00037260886,0.00015102775,0.000074853546,0.7889271,0.00039734767,0.19595717,0.00078533613,0.00005719561],"about_ca_topic_score_codex":0.014830358,"about_ca_topic_score_gemma":0.01789027,"teacher_disagreement_score":0.02256564,"about_ca_system_score_codex":0.0015491666,"about_ca_system_score_gemma":0.0018431487,"threshold_uncertainty_score":0.11934},"labels":[],"label_agreement":null},{"id":"W2154437541","doi":"10.1038/ng1033","title":"From patterns to pathways: gene expression data analysis comes of age","year":2002,"lang":"en","type":"review","venue":"Nature Genetics","topic":"Gene expression and cancer classification","field":"Biochemistry, Genetics and Molecular Biology","cited_by":581,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Women's Health Research Institute","funders":"","keywords":"Biology; DNA microarray; Gene expression profiling; Computational biology; Cluster analysis; Microarray analysis techniques; Profiling (computer programming); Microarray databases; Gene expression; Bioinformatics; Microarray; Gene chip analysis; Data science; Data mining; Gene; Genetics; Computer science; Machine learning","score_opus":0.0686333173855451,"score_gpt":0.348058894037556,"score_spread":0.27942557665201095,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2154437541","genre_codex":"review","genre_gemma":"review","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"review","genre_consensus":"review","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.00035187593,0.9502451,0.031497702,0.01360053,0.0020453061,0.000017098137,0.000175577,0.00026699985,0.0017998624],"genre_scores_gemma":[0.0034228582,0.95924705,0.025311967,0.0071848007,0.0028321529,0.000041251773,0.0002361734,0.000102662205,0.0016210488],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.99826604,0.00044743478,0.00020221178,0.00034237804,0.0006856739,0.000056290144],"domain_scores_gemma":[0.9870024,0.009421355,0.00033308577,0.00077680615,0.0020548059,0.00041155852],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0060103806,0.001418416,0.0041332105,0.0040223026,0.0006413599,0.0056886976,0.0030921015,0.0028943908,0.002888953],"category_scores_gemma":[0.010651807,0.00089219725,0.000827846,0.0064244913,0.007124946,0.0108087985,0.0019787466,0.008434493,0.003024864],"study_design_candidate":"not_applicable","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00008230729,0.000055892648,0.0008493721,0.0049784733,0.00016543367,0.00019951073,0.00025342466,0.0009572822,0.0017927137,0.040365815,0.06719047,0.88310933],"study_design_scores_gemma":[0.00003136655,0.000052065454,0.0011549625,0.002325683,0.00009080013,0.0015227842,0.00035421376,0.0010979275,0.001048878,0.19432507,0.7979014,0.000094739196],"about_ca_topic_score_codex":0.0025949627,"about_ca_topic_score_gemma":0.003195823,"teacher_disagreement_score":0.0060103806,"about_ca_system_score_codex":0.0016827593,"about_ca_system_score_gemma":0.0022278565,"threshold_uncertainty_score":0.031786323},"labels":[],"label_agreement":null},{"id":"W2155286781","doi":"10.1038/ng1104-1133","title":"The Collaborative Cross, a community resource for the genetic analysis of complex traits","year":2004,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Genetic Mapping and Diversity in Plants and Animals","field":"Biochemistry, Genetics and Molecular Biology","cited_by":1193,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Toronto Centre for Phenogenomics; University of Toronto; McGill University; Montreal Clinical Research Institute; Mount Sinai Hospital","funders":"Oak Ridge National Laboratory; National Heart, Lung, and Blood Institute; Medical Research Council; University of North Carolina at Chapel Hill; Health Science Center, University of Tennessee; University of California, Los Angeles; School of Medicine, Emory University; School of Medicine, New York University; National Institutes of Health; International Livestock Research Institute; National Institute on Alcohol Abuse and Alcoholism; Akademie Věd České Republiky; Rijksuniversiteit Groningen; National Cancer Institute; Universität Heidelberg; Vanderbilt University Medical Center; Cedars-Sinai Medical Center; Purdue University; Wellcome Trust; University of Cincinnati; David Geffen School of Medicine, University of California, Los Angeles; Medical Center, University of Rochester; Case Western Reserve University; Emory University; Northwestern University; University of Rochester; Johns Hopkins University; Advanced Scientific Computing Research; University of Wisconsin-Madison; Cincinnati Children's Hospital Medical Center; University at Buffalo; Helsingin Yliopisto; College of Medicine, University of Cincinnati; Shriners Hospitals for Children; McGill University; University of Pennsylvania; Hebrew University of Jerusalem; University of Toronto; Yale University; Vanderbilt University; University of Memphis; Thomas Jefferson University","keywords":"Biology; Trait; Complex disease; Resource (disambiguation); Computational biology; Genetic resources; Quantitative trait locus; Gene; Genetics; Data science; Biotechnology; Computer science","score_opus":0.01741388490512984,"score_gpt":0.28630492741754016,"score_spread":0.2688910425124103,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2155286781","genre_codex":"methods","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":null,"domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.15629376,0.0055839666,0.38768196,0.003663305,0.0015714652,0.002814227,0.20684087,0.0315689,0.20398152],"genre_scores_gemma":[0.14917728,0.003609441,0.47844175,0.0010116895,0.00062294095,0.0031227532,0.24519047,0.010959584,0.10786407],"study_design_codex":"design_other","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99835783,0.0004181309,0.000090858164,0.00026070417,0.0006820448,0.00019048585],"domain_scores_gemma":[0.98831487,0.002393862,0.0006760865,0.0037310293,0.0012154178,0.0036688438],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0039772405,0.0009610728,0.0012864708,0.0076836436,0.0025221317,0.0017282853,0.0026509685,0.00093074027,0.05837528],"category_scores_gemma":[0.007322009,0.00074163877,0.00049379276,0.0075760833,0.000488378,0.0014682694,0.0043659084,0.0017753299,0.013385171],"study_design_candidate":"bench_or_experimental","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0015963858,0.0009858459,0.012485668,0.0008299288,0.00031135272,0.0016823898,0.0016699088,0.0010333438,0.08283462,0.018785797,0.4138685,0.46391627],"study_design_scores_gemma":[0.0010093413,0.0004459168,0.050531145,0.00027814243,0.0003558758,0.0036392673,0.0005234668,0.0033274435,0.02419372,0.015795736,0.89962095,0.00027903618],"about_ca_topic_score_codex":0.008461483,"about_ca_topic_score_gemma":0.026521906,"teacher_disagreement_score":0.05837528,"about_ca_system_score_codex":0.0005757712,"about_ca_system_score_gemma":0.0042385007,"threshold_uncertainty_score":0.19528478},"labels":[],"label_agreement":null},{"id":"W2155758168","doi":"10.1038/ng1140","title":"C. elegans ORFeome version 1.1: experimental verification of the genome annotation and resource for proteome-scale protein expression","year":2003,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Genomics and Phylogenetic Studies","field":"Biochemistry, Genetics and Molecular Biology","cited_by":388,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"McGill University","funders":"","keywords":"ORFS; Biology; Caenorhabditis elegans; Open reading frame; Genetics; Interactome; Proteome; Genome; Computational biology; Gene; Genome project; Peptide sequence","score_opus":0.005460747412499646,"score_gpt":0.22771848328402045,"score_spread":0.2222577358715208,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2155758168","genre_codex":"dataset","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":null,"domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.35196826,0.0018100154,0.1097501,0.0006433389,0.00066055654,0.0013243732,0.49768198,0.02405418,0.0121072875],"genre_scores_gemma":[0.15239196,0.0010707534,0.2003993,0.00037450617,0.00007437174,0.0015549418,0.6271109,0.008666732,0.008356491],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99922633,0.000052319145,0.000104519255,0.0001988057,0.00030742804,0.00011065784],"domain_scores_gemma":[0.9987721,0.00023272201,0.00013979677,0.00031804657,0.00040746492,0.00012990551],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.001536632,0.0014584194,0.00134821,0.0027622879,0.0023099896,0.0010146188,0.0016107822,0.0012164754,0.004860378],"category_scores_gemma":[0.0024662884,0.0010475212,0.0012448106,0.0015920503,0.00053155323,0.0010603524,0.0012645809,0.0015892856,0.004396275],"study_design_candidate":"bench_or_experimental","study_design_consensus":"bench_or_experimental","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0015661084,0.00022389951,0.002355582,0.0013226769,0.00010554842,0.0004950048,0.00022967739,0.0006027528,0.94791114,0.001860922,0.024038484,0.01928825],"study_design_scores_gemma":[0.0004090997,0.00048398343,0.055360258,0.00045727618,0.00042555787,0.0018730727,0.00013759092,0.008852124,0.78285414,0.0020136458,0.14683114,0.0003021225],"about_ca_topic_score_codex":0.008748613,"about_ca_topic_score_gemma":0.017310677,"teacher_disagreement_score":0.008748613,"about_ca_system_score_codex":0.00096608856,"about_ca_system_score_gemma":0.0029190583,"threshold_uncertainty_score":0.017395377},"labels":[],"label_agreement":null},{"id":"W2156001353","doi":"10.1038/ng.302","title":"Increased LIS1 expression affects human and mouse brain development","year":2009,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Genomic variations and chromosomal abnormalities","field":"Biochemistry, Genetics and Molecular Biology","cited_by":220,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"North York General Hospital","funders":"Eunice Kennedy Shriver National Institute of Child Health and Human Development","keywords":"Lissencephaly; Biology; Gene duplication; Gene; Genetics; Cancer research","score_opus":0.004633571051173868,"score_gpt":0.23046678332483714,"score_spread":0.22583321227366326,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2156001353","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99241734,0.0013028013,0.0024610497,0.00021807697,0.00004300682,0.000014885612,0.0010426536,0.00024747604,0.0022526216],"genre_scores_gemma":[0.995388,0.0006300783,0.00096898095,0.000074173884,0.000013234034,0.000015140805,0.00057807384,0.00009566491,0.0022366429],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9997476,0.000040953553,0.000030237861,0.000078134435,0.00006020695,0.000042818217],"domain_scores_gemma":[0.9997267,0.00007103375,0.00010913348,0.000029270923,0.000015864409,0.000047893805],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00017662367,0.00054797187,0.00036505316,0.0011170385,0.0002852339,0.000522547,0.00032680787,0.00064218894,0.0033200886],"category_scores_gemma":[0.00028222962,0.00040087715,0.00038461093,0.00047861968,0.0007081655,0.00022828368,0.00046709177,0.0006358684,0.00050422107],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0003771596,0.00002116418,0.00095628126,0.0000436597,0.000026012682,0.00079930277,0.000032180673,0.00021676398,0.9949255,0.0003218907,0.000115154,0.002165012],"study_design_scores_gemma":[0.000054257293,0.0002599846,0.030020695,0.000016101596,0.00016205065,0.006000734,0.00009084428,0.0012341532,0.9571875,0.00042189445,0.004528687,0.000023148916],"about_ca_topic_score_codex":0.0012467959,"about_ca_topic_score_gemma":0.0015188833,"teacher_disagreement_score":0.0033200886,"about_ca_system_score_codex":0.00042519072,"about_ca_system_score_gemma":0.00031335675,"threshold_uncertainty_score":0.011106849},"labels":[],"label_agreement":null},{"id":"W2156435321","doi":"10.1038/ng1683","title":"Identification of the gene responsible for methylmalonic aciduria and homocystinuria, cblC type","year":2005,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Folate and B Vitamins Research","field":"Medicine","cited_by":376,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"McGill University and Génome Québec Innovation Centre; Hospital for Sick Children; Montreal Neurological Institute and Hospital; SickKids Foundation; University of Toronto; McGill University Health Centre; University of Calgary; McGill University","funders":"","keywords":"Homocystinuria; Biology; Cobalamin; Genetics; Methylmalonic aciduria; Locus (genetics); Gene; Vitamin B12; Biochemistry; Methionine","score_opus":0.01671479245128065,"score_gpt":0.3385090794829279,"score_spread":0.32179428703164725,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2156435321","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99293256,0.00092295907,0.002052988,0.0008731607,0.00018794878,0.000047173617,0.00116806,0.0001161356,0.0016989963],"genre_scores_gemma":[0.99389243,0.00030401384,0.0017329234,0.00018955067,0.00006860908,0.000022780672,0.00079379056,0.000037106893,0.0029588088],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9998184,0.000011668159,0.000025634245,0.000054791526,0.000053650037,0.000035943198],"domain_scores_gemma":[0.9994159,0.00023279009,0.00008643631,0.000036908517,0.00007505865,0.00015285278],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00015671195,0.0006232089,0.00053058035,0.0015639657,0.0005276685,0.00045074802,0.0006375548,0.0014777699,0.0026855948],"category_scores_gemma":[0.0009901305,0.00023318743,0.00064595364,0.0005899098,0.0006209458,0.00020882075,0.0002975077,0.0010882682,0.0004405989],"study_design_candidate":"bench_or_experimental","study_design_consensus":"bench_or_experimental","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0020773285,0.00030763203,0.037180442,0.00022672919,0.00019298104,0.109864496,0.0005800637,0.00052590127,0.8292054,0.0025810483,0.0014282465,0.015829789],"study_design_scores_gemma":[0.00048581263,0.00085618894,0.26877752,0.00008498412,0.0006099677,0.20120722,0.0008279105,0.0043274825,0.5086253,0.0028076004,0.011277008,0.00011307958],"about_ca_topic_score_codex":0.0042906683,"about_ca_topic_score_gemma":0.0025064955,"teacher_disagreement_score":0.0042906683,"about_ca_system_score_codex":0.00062549836,"about_ca_system_score_gemma":0.00063178124,"threshold_uncertainty_score":0.008984268},"labels":[],"label_agreement":null},{"id":"W2156459362","doi":"10.1038/ng.873","title":"Interaction between ERAP1 and HLA-B27 in ankylosing spondylitis implicates peptide handling in the mechanism for HLA-B27 in disease susceptibility","year":2011,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Spondyloarthritis Studies and Treatments","field":"Medicine","cited_by":907,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Memorial University of Newfoundland; University of Alberta; University of Toronto","funders":"National Health and Medical Research Council; Canadian Institutes of Health Research; National Institute of Arthritis and Musculoskeletal and Skin Diseases; Medical Research Council; Versus Arthritis; Karolinska Institutet; Arthritis Society; Stiftelsen för Strategisk Forskning; Knut och Alice Wallenbergs Stiftelse; Australian Cancer Research Foundation; National Center for Research Resources; Ontario Genomics Institute; Università di Cagliari; National Institute for Health and Care Research; National Institutes of Health; Ontario Genomics; Genome Canada; GlaxoSmithKline; Cedars-Sinai Medical Center; Ontario Innovation Trust; Lions Medical Research Foundation; Wellcome Trust","keywords":"Ankylosing spondylitis; HLA-B27; Human leukocyte antigen; Biology; Immunology; Disease; Mechanism (biology); Spondylitis; Genetics; Medicine; Antigen; Internal medicine","score_opus":0.03268966452519435,"score_gpt":0.31222607871018293,"score_spread":0.2795364141849886,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2156459362","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99251467,0.0033157002,0.0015075561,0.000511717,0.000044814144,0.0000055373216,0.00012068497,0.000048773272,0.0019304162],"genre_scores_gemma":[0.99755645,0.00047549736,0.0005242726,0.00006887462,0.00002193136,0.0000053503986,0.00008069701,0.000010934409,0.0012559657],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9997855,0.00006664046,0.000015243821,0.000040233423,0.00004384369,0.00004852244],"domain_scores_gemma":[0.9997099,0.0001203153,0.0000705561,0.000034118315,0.000018015457,0.0000471237],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0003990394,0.00026005128,0.00027907788,0.00030003968,0.00021616697,0.0003705268,0.0003591332,0.00046630678,0.003730148],"category_scores_gemma":[0.0005986585,0.00026768923,0.00027882628,0.00015344998,0.00028785734,0.0002782898,0.00036815245,0.00068953104,0.000592171],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.001444076,0.000101362064,0.018844428,0.00013034997,0.00016250776,0.0030495732,0.00013424449,0.000605773,0.95635676,0.0021353562,0.0007137679,0.01632171],"study_design_scores_gemma":[0.00046883506,0.0017791213,0.3173279,0.0000813841,0.00041047737,0.02796779,0.00041727794,0.009367688,0.621404,0.006459853,0.0142491255,0.00006656348],"about_ca_topic_score_codex":0.00026766496,"about_ca_topic_score_gemma":0.00023186342,"teacher_disagreement_score":0.003730148,"about_ca_system_score_codex":0.000228332,"about_ca_system_score_gemma":0.00018746966,"threshold_uncertainty_score":0.01247859},"labels":[],"label_agreement":null},{"id":"W2156625453","doi":"10.1038/ng.255","title":"Male-pattern baldness susceptibility locus at 20p11","year":2008,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Hair Growth and Disorders","field":"Medicine","cited_by":139,"is_retracted":false,"has_abstract":false,"route_ca_aff":false,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"","funders":"Canadian Institutes of Health Research; King's College London; National Institute for Health and Care Research; Wellcome Trust; GlaxoSmithKline","keywords":"Male-pattern baldness; Biology; Locus (genetics); Androgen receptor; Allele; Genetics; Odds ratio; Genome-wide association study; Hair loss; Androgen; X chromosome; Genotype; Internal medicine; Single-nucleotide polymorphism; Endocrinology; Gene; Anatomy; Medicine","score_opus":0.012021634142335437,"score_gpt":0.26095354125442105,"score_spread":0.24893190711208563,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2156625453","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9562757,0.0030230852,0.006293354,0.0038727643,0.00051221263,0.000106781816,0.0020733695,0.0003697917,0.027472982],"genre_scores_gemma":[0.98797077,0.0008133714,0.0013543234,0.00028703435,0.00016840488,0.000027590122,0.00046865694,0.00004389159,0.00886596],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.99969447,0.00006482085,0.000022742977,0.00008365721,0.000080986356,0.00005329181],"domain_scores_gemma":[0.99947375,0.00021241223,0.00012558847,0.00003683983,0.000038464514,0.00011291623],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00020162915,0.0009204742,0.00057307316,0.0017761337,0.0007130777,0.0005463949,0.00054903893,0.0012827709,0.015311609],"category_scores_gemma":[0.0010795657,0.00027947992,0.0005240731,0.00070309243,0.00043300798,0.0003256916,0.00049379654,0.00067795557,0.0010186067],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0027019498,0.00022600524,0.06137239,0.00028157537,0.00033689398,0.19613388,0.0010458513,0.001044529,0.6354178,0.011752559,0.007686081,0.08200048],"study_design_scores_gemma":[0.00061679917,0.0006708663,0.3545674,0.00023016363,0.0007648907,0.46364978,0.0009394477,0.0023984148,0.12207621,0.008014205,0.045933664,0.00013815725],"about_ca_topic_score_codex":0.0015630338,"about_ca_topic_score_gemma":0.0017315586,"teacher_disagreement_score":0.015311609,"about_ca_system_score_codex":0.00043042374,"about_ca_system_score_gemma":0.00032014534,"threshold_uncertainty_score":0.051222384},"labels":[],"label_agreement":null},{"id":"W2157783878","doi":"10.1038/ng.2253","title":"Mutations in ISPD cause Walker-Warburg syndrome and defective glycosylation of α-dystroglycan","year":2012,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Heat shock proteins research","field":"Biochemistry, Genetics and Molecular Biology","cited_by":212,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Hospital for Sick Children; Mount Sinai Hospital; University of Toronto","funders":"Hersenstichting; Medical Research Council; ZonMw; National Health and Medical Research Council; European Commission; Wellcome Trust","keywords":"Biology; Dystroglycan; Glycosylation; Genetics; Zebrafish; Gene; Phenotype; Muscular dystrophy; Laminin","score_opus":0.011003363769256643,"score_gpt":0.3025088702623575,"score_spread":0.29150550649310086,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2157783878","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9968629,0.00024528118,0.0012237112,0.000121058074,0.00004782233,0.00002001979,0.00026850225,0.00006538121,0.0011454971],"genre_scores_gemma":[0.9979243,0.00017740163,0.00097561127,0.00004038389,0.000030116353,0.000012718995,0.00024060397,0.000024264778,0.0005745122],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99981767,0.000027270167,0.000041588024,0.000030208936,0.000058294427,0.000024978208],"domain_scores_gemma":[0.99949646,0.0001361936,0.00016813815,0.000029806326,0.00002027086,0.00014912417],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00016726203,0.001849489,0.00041178745,0.0012068403,0.00038598297,0.00036858927,0.00041568867,0.0010036865,0.0019832784],"category_scores_gemma":[0.0007846005,0.00039080795,0.0005332375,0.00090588664,0.0011335124,0.0002673913,0.00070146547,0.00060257746,0.0005665541],"study_design_candidate":"bench_or_experimental","study_design_consensus":"bench_or_experimental","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.001993696,0.0002883364,0.034444217,0.00030038852,0.00039203351,0.24530311,0.00075159565,0.0023654352,0.69420063,0.004012748,0.0015985396,0.01434931],"study_design_scores_gemma":[0.00072880543,0.0011783908,0.21351576,0.00017633694,0.0008291426,0.39400694,0.0009480491,0.010921832,0.36001977,0.0046102414,0.012894788,0.0001699387],"about_ca_topic_score_codex":0.0011677648,"about_ca_topic_score_gemma":0.0013440998,"teacher_disagreement_score":0.0019832784,"about_ca_system_score_codex":0.0005434352,"about_ca_system_score_gemma":0.00037862943,"threshold_uncertainty_score":0.006634772},"labels":[],"label_agreement":null},{"id":"W2159422401","doi":"10.1038/ng.520","title":"New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk","year":2010,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Genetic Associations and Epidemiology","field":"Biochemistry, Genetics and Molecular Biology","cited_by":2228,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Ottawa; McGill University and Génome Québec Innovation Centre; McGill University","funders":"National Institute of Diabetes and Digestive and Kidney Diseases; Economic and Social Research Council; National Institute for Health and Care Research; British Heart Foundation; Wellcome Trust","keywords":"Biology; Insulin resistance; Type 2 diabetes; Glucose homeostasis; Internal medicine; Genome-wide association study; Glycemic; Endocrinology; Diabetes mellitus; Genetic association; Insulin; Candidate gene; Impaired fasting glucose; Genetics; Impaired glucose tolerance; Gene; Genotype; Single-nucleotide polymorphism; Medicine","score_opus":0.00607221798456904,"score_gpt":0.2625152312558718,"score_spread":0.25644301327130276,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2159422401","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9901433,0.0038989577,0.0026845206,0.0008396787,0.00014633728,0.000013563621,0.00058042683,0.000050122915,0.00164309],"genre_scores_gemma":[0.99415565,0.0012325528,0.00297318,0.000173111,0.0002789771,0.0000148329955,0.00028459885,0.00002734548,0.0008596608],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9987909,0.00050031586,0.00013912324,0.00027493047,0.0002034958,0.00009128763],"domain_scores_gemma":[0.99547845,0.0025869606,0.00096280867,0.0003727375,0.0002466512,0.0003525388],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.001317407,0.0011859874,0.0006923091,0.0024087776,0.00049410964,0.0012126553,0.0008274773,0.0014045634,0.003555375],"category_scores_gemma":[0.0046097822,0.0006190806,0.0012211744,0.003120756,0.00072535337,0.00054075796,0.0005362393,0.0011410813,0.00026071412],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.004957694,0.00027656672,0.9323227,0.00017429974,0.0027682376,0.005808795,0.0004930646,0.0012422788,0.026892494,0.0020704363,0.00069692114,0.022296416],"study_design_scores_gemma":[0.0002675028,0.00027689643,0.9830019,0.000054515353,0.0018714588,0.004879209,0.00023647734,0.0019286165,0.0025819128,0.0034880145,0.0013624817,0.000051024308],"about_ca_topic_score_codex":0.002762313,"about_ca_topic_score_gemma":0.0022655139,"teacher_disagreement_score":0.003555375,"about_ca_system_score_codex":0.00029996046,"about_ca_system_score_gemma":0.00026603744,"threshold_uncertainty_score":0.011893928},"labels":[],"label_agreement":null},{"id":"W2160435411","doi":"10.1038/ng.474","title":"Microduplications of 16p11.2 are associated with schizophrenia","year":2009,"lang":"en","type":"review","venue":"Nature Genetics","topic":"Genomic variations and chromosomal abnormalities","field":"Biochemistry, Genetics and Molecular Biology","cited_by":736,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Ontario Institute for Cancer Research","funders":"National Institute of Dental and Craniofacial Research; National Center for Research Resources; National Institute of General Medical Sciences; National Institute of Mental Health; National Institutes of Health; Eunice Kennedy Shriver National Institute of Child Health and Human Development; U.S. Public Health Service; Wellcome Trust","keywords":"Autism; Schizophrenia (object-oriented programming); Cohort; Copy-number variation; Medicine; Genetic association; Pediatrics; Psychiatry; Genetics; Biology; Internal medicine; Single-nucleotide polymorphism; Genotype; Genome; Gene","score_opus":0.011227188313439588,"score_gpt":0.2630723338037317,"score_spread":0.2518451454902921,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2160435411","genre_codex":"review","genre_gemma":"review","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"review","genre_consensus":"review","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.0006114899,0.99705553,0.00041466154,0.00056784746,0.00018493312,0.0000046526106,0.00005795602,0.000020754462,0.0010822573],"genre_scores_gemma":[0.003230748,0.99503666,0.00039871532,0.00019072632,0.00024904503,0.000006219666,0.000103085375,0.0000029049913,0.0007819521],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.9998129,0.000027962662,0.00003155714,0.00004214323,0.000066430664,0.000019064351],"domain_scores_gemma":[0.99966514,0.00014807943,0.000088383655,0.000011101023,0.000058081667,0.000029234416],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00047624588,0.0010186514,0.0014461756,0.0017572022,0.00018248959,0.0005454339,0.0010692669,0.0010439716,0.0024207283],"category_scores_gemma":[0.0007043268,0.00028947697,0.00031459625,0.002035058,0.0005464179,0.00053962745,0.0005663308,0.0010707863,0.0014211196],"study_design_candidate":"not_applicable","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00016066748,0.00002594486,0.0010949754,0.005299348,0.00016728695,0.002090469,0.000035604204,0.00048146746,0.0033592025,0.002026097,0.028892264,0.9563667],"study_design_scores_gemma":[0.000090513684,0.00010710281,0.010319602,0.003455482,0.0005464976,0.027604595,0.000116302246,0.0002082705,0.0028630958,0.0047808657,0.94984907,0.000058685542],"about_ca_topic_score_codex":0.0014478782,"about_ca_topic_score_gemma":0.0022694233,"teacher_disagreement_score":0.0024207283,"about_ca_system_score_codex":0.0005297407,"about_ca_system_score_gemma":0.0007345326,"threshold_uncertainty_score":0.008098125},"labels":[],"label_agreement":null},{"id":"W2160868309","doi":"10.1038/ng1307","title":"A tiling resolution DNA microarray with complete coverage of the human genome","year":2004,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Genomic variations and chromosomal abnormalities","field":"Biochemistry, Genetics and Molecular Biology","cited_by":629,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"BC Cancer Agency","funders":"Genome Canada","keywords":"Tiling array; Biology; Genome; Genetics; Comparative genomic hybridization; Human genome; Computational biology; Gene; DNA microarray; Gene expression","score_opus":0.006602439607936191,"score_gpt":0.21318162950107447,"score_spread":0.20657918989313828,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2160868309","genre_codex":"methods","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":null,"domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.24703263,0.0025865096,0.69941914,0.0031824943,0.00088355213,0.0005517655,0.013049884,0.019075064,0.014219022],"genre_scores_gemma":[0.19303763,0.0011443852,0.7788291,0.0013395383,0.00017129997,0.0010976343,0.01294206,0.00065483694,0.010783569],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9992619,0.00010234171,0.000038795588,0.00024899188,0.0002445908,0.000103376304],"domain_scores_gemma":[0.9995289,0.00014684205,0.000037728994,0.0001273407,0.00006284722,0.00009633003],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.000460811,0.0005564118,0.0009734784,0.00070099,0.00056804885,0.0005165964,0.0008655694,0.0011405483,0.0062941597],"category_scores_gemma":[0.0007742259,0.0007222604,0.0006645224,0.0007832753,0.0002788688,0.00061964756,0.0006338149,0.0013008787,0.003158615],"study_design_candidate":"bench_or_experimental","study_design_consensus":"bench_or_experimental","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00010504815,0.000022501792,0.00011387959,0.00005658612,0.000011022046,0.0000329093,0.000010943138,0.0003944889,0.9905409,0.00034985994,0.0010911864,0.0072706263],"study_design_scores_gemma":[0.00008584519,0.0003963321,0.0037552197,0.000014441216,0.00006771861,0.00072608975,0.000025819243,0.014519988,0.95250624,0.0011481404,0.026713733,0.000040464598],"about_ca_topic_score_codex":0.00053656707,"about_ca_topic_score_gemma":0.0011206537,"teacher_disagreement_score":0.0062941597,"about_ca_system_score_codex":0.00046705038,"about_ca_system_score_gemma":0.0005840721,"threshold_uncertainty_score":0.021056056},"labels":[],"label_agreement":null},{"id":"W2161527093","doi":"10.1038/ng.940","title":"Genome-wide association study identifies five new schizophrenia loci","year":2011,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Genetic Associations and Epidemiology","field":"Biochemistry, Genetics and Molecular Biology","cited_by":1954,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Toronto","funders":"National Institute of General Medical Sciences; National Institute of Mental Health; National Institutes of Health; National Cancer Institute; National Heart, Lung, and Blood Institute; Wellcome Trust","keywords":"Biology; Genome-wide association study; Genetics; Genetic association; Genome; Schizophrenia (object-oriented programming); Association (psychology); Computational biology; Single-nucleotide polymorphism; Gene; Genotype; Psychiatry","score_opus":0.012376932267391597,"score_gpt":0.25833770676785206,"score_spread":0.24596077450046047,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2161527093","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9972186,0.00047534495,0.0011299669,0.00020336387,0.000020142817,0.00000937839,0.0003620918,0.000027178066,0.00055392203],"genre_scores_gemma":[0.998044,0.00017810473,0.0009761499,0.000061685336,0.000012707788,0.000006992894,0.00031039867,0.000008833509,0.00040110887],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99946994,0.00010941064,0.000060661732,0.00015235733,0.00012432078,0.00008344355],"domain_scores_gemma":[0.99831235,0.00056714437,0.0005065169,0.00010710663,0.00014297053,0.0003639764],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0009640005,0.0006029259,0.0004023546,0.0017505469,0.00079173903,0.0006263676,0.00062327395,0.0007012576,0.0022957418],"category_scores_gemma":[0.0015142319,0.00029923182,0.0006299996,0.0014141721,0.0006625967,0.000253252,0.00075435353,0.00080092007,0.0002404596],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0041867895,0.0003742224,0.90644664,0.000097616205,0.0011580448,0.0024998044,0.00049182045,0.0002931852,0.0666407,0.0010078847,0.0006745659,0.016128695],"study_design_scores_gemma":[0.00017224501,0.00030696034,0.99045753,0.000017553495,0.0006312175,0.002217191,0.0002478221,0.0004765807,0.0036632512,0.0008602621,0.0009208191,0.00002844042],"about_ca_topic_score_codex":0.005414095,"about_ca_topic_score_gemma":0.008310766,"teacher_disagreement_score":0.005414095,"about_ca_system_score_codex":0.00037947085,"about_ca_system_score_gemma":0.0007929686,"threshold_uncertainty_score":0.010765195},"labels":[],"label_agreement":null},{"id":"W2161827216","doi":"10.1038/ng.1049","title":"Genome-wide association analysis identifies three new breast cancer susceptibility loci","year":2012,"lang":"en","type":"review","venue":"Nature Genetics","topic":"BRCA gene mutations in cancer","field":"Biochemistry, Genetics and Molecular Biology","cited_by":284,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Toronto; Lunenfeld-Tanenbaum Research Institute; Cancer Care Ontario; Mount Sinai Hospital","funders":"National Cancer Institute; National Institute for Health and Care Research; Cancer Research UK; Wellcome Trust","keywords":"Breast cancer; Genome-wide association study; Biology; Genetic association; Estrogen receptor; Genetic architecture; Genetics; Cancer; Disease; Oncology; Single-nucleotide polymorphism; Internal medicine; Gene; Quantitative trait locus; Genotype; Medicine","score_opus":0.018941359161227193,"score_gpt":0.3224792663090794,"score_spread":0.3035379071478522,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2161827216","genre_codex":"review","genre_gemma":"review","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"review","genre_consensus":"review","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.00040529433,0.99676836,0.0007936084,0.0008536895,0.0001822682,0.00000471231,0.000067319655,0.000023811088,0.00090088893],"genre_scores_gemma":[0.002346574,0.99473333,0.0009839246,0.0007212991,0.00031496605,0.000009968523,0.00013652351,0.000004170366,0.000749192],"study_design_codex":"design_other","study_design_gemma":"observational","domain_scores_codex":[0.9997218,0.000034802037,0.000028649825,0.00007933808,0.00010942391,0.000025967964],"domain_scores_gemma":[0.999432,0.00027951118,0.00007937554,0.000020296171,0.00013315906,0.00005561774],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0009578404,0.0012230817,0.0016751982,0.0016699368,0.00021500333,0.0010135942,0.0012626131,0.0016010047,0.0016871731],"category_scores_gemma":[0.0009888744,0.00033488273,0.0004782006,0.0019810023,0.00064331334,0.0007161983,0.0005985233,0.0019526464,0.0012585722],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00013571238,0.000059542825,0.0015298354,0.004390528,0.0001930566,0.00056761655,0.000028043705,0.00032431292,0.0046963883,0.0025846285,0.029312128,0.9561783],"study_design_scores_gemma":[0.000100786325,0.000104219835,0.0109249,0.0025082175,0.00083251315,0.005804099,0.000091695874,0.00031217636,0.0033658796,0.006833639,0.969043,0.000078971134],"about_ca_topic_score_codex":0.0015574457,"about_ca_topic_score_gemma":0.0032318209,"teacher_disagreement_score":0.0016871731,"about_ca_system_score_codex":0.0006734793,"about_ca_system_score_gemma":0.0010273242,"threshold_uncertainty_score":0.0056441426},"labels":[],"label_agreement":null},{"id":"W2161990844","doi":"10.1038/ng.2478","title":"Emergence and global spread of epidemic healthcare-associated Clostridium difficile","year":2012,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Clostridium difficile and Clostridium perfringens research","field":"Medicine","cited_by":740,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Calgary","funders":"Medical Research Council; National Institute for Health and Care Research; Wellcome Trust","keywords":"Biology; Lineage (genetic); Outbreak; Clostridium difficile; Global health; Phylogenetic tree; Population; Evolutionary biology; Genetics; Health care; Virology; Antibiotics; Environmental health; Economic growth; Gene; Medicine","score_opus":0.026122073559230328,"score_gpt":0.34322626998633876,"score_spread":0.3171041964271084,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2161990844","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9809724,0.0050644884,0.0013610874,0.004776559,0.000104541126,0.000015889644,0.0004069937,0.00003453277,0.0072635645],"genre_scores_gemma":[0.99538124,0.0027590895,0.0005207988,0.0005144374,0.00011852862,0.0000034192199,0.00022556428,0.000010240844,0.00046664142],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.999383,0.0001629671,0.00003758498,0.00014451778,0.00013106767,0.00014096647],"domain_scores_gemma":[0.9987173,0.00018251124,0.00053709425,0.00012435472,0.00027340083,0.00016538202],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.000861194,0.00020573847,0.00020050151,0.00100792,0.0003223873,0.0011558441,0.0002425224,0.0006320188,0.0025900379],"category_scores_gemma":[0.0023341975,0.00015564272,0.0002330354,0.0012570783,0.0006709986,0.00095482584,0.0007601543,0.001066946,0.00023129971],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00054758077,0.00010221042,0.8891332,0.0001158483,0.00009645099,0.001019802,0.0010913941,0.00083554647,0.008674544,0.0043895915,0.0044060615,0.08958783],"study_design_scores_gemma":[0.00003938909,0.00019914274,0.9819456,0.00008382388,0.0000528541,0.002048433,0.0027090244,0.0010339542,0.00057525607,0.0025544686,0.008738944,0.000019123676],"about_ca_topic_score_codex":0.005797844,"about_ca_topic_score_gemma":0.006410894,"teacher_disagreement_score":0.005797844,"about_ca_system_score_codex":0.00079027447,"about_ca_system_score_gemma":0.00062968413,"threshold_uncertainty_score":0.011528194},"labels":[],"label_agreement":null},{"id":"W2162079601","doi":"10.1038/ng.3400","title":"The genomic landscape of juvenile myelomonocytic leukemia","year":2015,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Acute Myeloid Leukemia Research","field":"Medicine","cited_by":309,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Hospital for Sick Children","funders":"National Cancer Institute","keywords":"Biology; Juvenile myelomonocytic leukemia; Juvenile; Chronic myelomonocytic leukemia; Genetics; Evolutionary biology; Leukemia; Computational biology; Immunology; Myelodysplastic syndromes","score_opus":0.02087007176139491,"score_gpt":0.30146217795745617,"score_spread":0.28059210619606123,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2162079601","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.97391164,0.009043704,0.0014686445,0.0073224423,0.000059485606,0.00000866016,0.0009647192,0.000046447985,0.0071743173],"genre_scores_gemma":[0.9956487,0.0025475551,0.0003425004,0.00046718118,0.0000959266,0.0000030099832,0.00027630673,0.0000141574355,0.0006046506],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9997273,0.00006536168,0.000012500552,0.000067091874,0.000063274754,0.00006445859],"domain_scores_gemma":[0.9996132,0.00014070558,0.0001263287,0.000021008933,0.000029891511,0.000068898975],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00017427126,0.00014677517,0.00018807178,0.0007255148,0.00041324852,0.00080556795,0.00023791255,0.0003863565,0.002280198],"category_scores_gemma":[0.0010185412,0.00010296457,0.00012668327,0.0009256675,0.00059087743,0.0003952883,0.00046291435,0.00048622943,0.00016722376],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0011740183,0.00010726464,0.50559634,0.00037838222,0.000279539,0.009060227,0.0021965231,0.004570712,0.20022999,0.04223702,0.009021665,0.22514828],"study_design_scores_gemma":[0.00006942775,0.00021874481,0.86549395,0.00018945921,0.00036394125,0.011972256,0.0028758417,0.0025622894,0.009460651,0.055430893,0.051308934,0.000053638043],"about_ca_topic_score_codex":0.0019074033,"about_ca_topic_score_gemma":0.0028676467,"teacher_disagreement_score":0.002280198,"about_ca_system_score_codex":0.00049097737,"about_ca_system_score_gemma":0.0004290493,"threshold_uncertainty_score":0.0076280236},"labels":[],"label_agreement":null},{"id":"W2163749231","doi":"10.1038/ng.3434","title":"Genetic association analyses implicate aberrant regulation of innate and adaptive immunity genes in the pathogenesis of systemic lupus erythematosus","year":2015,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Systemic Lupus Erythematosus Research","field":"Medicine","cited_by":1094,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Université de Montréal; Montreal Heart Institute; University Health Network","funders":"National Institute of Environmental Health Sciences; National Cancer Institute; National Institute on Aging; Instituto de Salud Carlos III; Howard Hughes Medical Institute; Versus Arthritis; National Heart, Lung, and Blood Institute; Vetenskapsrådet; European Commission; European Science Foundation; King's College London; Canadian Institutes of Health Research; China Scholarship Council; National Institute for Health and Care Research; National Human Genome Research Institute; Wellcome Trust; Academy of Medical Sciences","keywords":"Biology; Genome-wide association study; Genetics; Expression quantitative trait loci; Genetic association; Immunology; Immune system; Gene; Allele; Imputation (statistics); Innate immune system; Acquired immune system; Single-nucleotide polymorphism; Genotype","score_opus":0.04897638029925949,"score_gpt":0.33328327265393065,"score_spread":0.28430689235467116,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2163749231","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9968822,0.0008702164,0.0012652026,0.00018030898,0.000017713262,0.000004100294,0.00012301024,0.000024970155,0.00063220324],"genre_scores_gemma":[0.99862885,0.00032438646,0.0007074476,0.000046853642,0.000035516718,0.0000028009342,0.00006201187,0.000008860376,0.00018332417],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9989918,0.00033090624,0.00011141198,0.00026219187,0.00020170257,0.00010192527],"domain_scores_gemma":[0.9985682,0.0005972664,0.00053546706,0.00009244056,0.00008505982,0.00012153793],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00069346465,0.00046208198,0.00037914014,0.0013191873,0.00029884436,0.00055805454,0.00038246284,0.000582158,0.0015794053],"category_scores_gemma":[0.0012238584,0.00024116495,0.00042471127,0.0010178816,0.00061819295,0.00021108604,0.00034246565,0.0006974582,0.00018501023],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0031383382,0.00020713813,0.59652436,0.00014751367,0.000740787,0.0035588907,0.00023832076,0.0011514619,0.367983,0.0021704754,0.00042509852,0.02371459],"study_design_scores_gemma":[0.00013572538,0.00023527248,0.963713,0.000033177836,0.000691232,0.006022944,0.0001451285,0.0028051687,0.022721576,0.0021904525,0.0012792062,0.00002712864],"about_ca_topic_score_codex":0.0006350505,"about_ca_topic_score_gemma":0.0007008497,"teacher_disagreement_score":0.0015794053,"about_ca_system_score_codex":0.00023198084,"about_ca_system_score_gemma":0.00020247741,"threshold_uncertainty_score":0.0052836537},"labels":[],"label_agreement":null},{"id":"W2163955717","doi":"10.1038/ng.536","title":"Common variants at 7p21 are associated with frontotemporal lobar degeneration with TDP-43 inclusions","year":2010,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Amyotrophic Lateral Sclerosis Research","field":"Medicine","cited_by":609,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Toronto; St. Michael's Hospital; Vancouver General Hospital; University of British Columbia","funders":"National Center for Research Resources; National Institute of Neurological Disorders and Stroke; Canadian Institutes of Health Research; National Institute on Aging; National Institutes of Health; Wellcome Trust","keywords":"Frontotemporal lobar degeneration; Biology; Genetics; Single-nucleotide polymorphism; Genome-wide association study; Frontotemporal dementia; TARDBP; Amyotrophic lateral sclerosis; Linkage disequilibrium; Genetic association; Allele; Haplotype; Dementia; Medicine; Gene; Pathology; Disease; Genotype; Mutant; SOD1","score_opus":0.014297540720144478,"score_gpt":0.2830952973064609,"score_spread":0.2687977565863164,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2163955717","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99409854,0.00070722925,0.001171253,0.00034544602,0.00012781589,0.000053353084,0.00079369056,0.00009946256,0.002603244],"genre_scores_gemma":[0.9970395,0.00018822342,0.00087124604,0.00011238658,0.00019775654,0.000028396329,0.00041268193,0.00004799594,0.0011017506],"study_design_codex":"case_report","study_design_gemma":"observational","domain_scores_codex":[0.99875164,0.00017471255,0.00023569814,0.00031479556,0.00036755943,0.00015561606],"domain_scores_gemma":[0.996518,0.0012518334,0.0013560263,0.00020059077,0.0002467984,0.00042668486],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00059164263,0.0035389555,0.0016306263,0.0047799745,0.0022290759,0.0011228246,0.0019999954,0.0044695614,0.00773746],"category_scores_gemma":[0.003262586,0.0007254446,0.0017476078,0.004045675,0.0016018357,0.0008242944,0.0014141842,0.001277714,0.001898638],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0074069407,0.00064417213,0.12148495,0.00037411254,0.0020792673,0.64090496,0.0025343348,0.0016150137,0.19627425,0.0021385092,0.0042705503,0.020272948],"study_design_scores_gemma":[0.0006520263,0.00090296095,0.39485586,0.00013875659,0.0023116725,0.5676439,0.0009029631,0.002824354,0.019425338,0.004634542,0.005448203,0.00025954915],"about_ca_topic_score_codex":0.0028362467,"about_ca_topic_score_gemma":0.003696339,"teacher_disagreement_score":0.00773746,"about_ca_system_score_codex":0.0005950139,"about_ca_system_score_gemma":0.00046791395,"threshold_uncertainty_score":0.02588439},"labels":[],"label_agreement":null},{"id":"W2163969089","doi":"10.1038/ng.2795","title":"Common variants associated with plasma triglycerides and risk for coronary artery disease","year":2013,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Diabetes, Cardiovascular Risks, and Lipoproteins","field":"Medicine","cited_by":906,"is_retracted":false,"has_abstract":false,"route_ca_aff":false,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"","funders":"National Institute of Diabetes and Digestive and Kidney Diseases; National Heart, Lung, and Blood Institute; Medical Research Council; National Institutes of Health; Fondation Leducq; British Heart Foundation; National Center for Advancing Translational Sciences; National Human Genome Research Institute; Wellcome Trust; Canadian Institutes of Health Research; Donovan Family Foundation; Massachusetts General Hospital; National Institute for Health and Care Research; Economic and Social Research Council","keywords":"Biology; Coronary artery disease; Internal medicine; Disease; Cardiology; Genetics; Medicine","score_opus":0.007335701503249582,"score_gpt":0.222966489003584,"score_spread":0.21563078750033443,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2163969089","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9887659,0.0031623428,0.0029726434,0.00081439526,0.00021594405,0.000036258356,0.0010710215,0.00010204716,0.0028593687],"genre_scores_gemma":[0.99762326,0.00032322493,0.00091267127,0.00012984348,0.00015546056,0.0000123543,0.00029922457,0.000028236187,0.00051582826],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99866056,0.00032145728,0.00023009516,0.00039591515,0.00023956891,0.00015241904],"domain_scores_gemma":[0.9980076,0.0008174693,0.00061126443,0.00016285911,0.00014125714,0.00025953876],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00064852746,0.0014753831,0.0008127437,0.0017879988,0.0007819788,0.0009568417,0.000878032,0.0020156242,0.006645777],"category_scores_gemma":[0.002582304,0.0005306071,0.0014739577,0.0022392399,0.0006370057,0.00042849692,0.0006104358,0.0014765869,0.0004474792],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.010340291,0.0005259018,0.80577487,0.00041670396,0.008027734,0.036929294,0.0015240291,0.0028478506,0.095245376,0.0067403116,0.0037021248,0.027925543],"study_design_scores_gemma":[0.0008992456,0.00045496508,0.9443803,0.0002777475,0.00488097,0.025086401,0.0005679589,0.0053965338,0.0060220766,0.0080748685,0.0037974895,0.00016141847],"about_ca_topic_score_codex":0.0054617063,"about_ca_topic_score_gemma":0.0061929575,"teacher_disagreement_score":0.006645777,"about_ca_system_score_codex":0.00039254985,"about_ca_system_score_gemma":0.0003769601,"threshold_uncertainty_score":0.022232294},"labels":[],"label_agreement":null},{"id":"W2165019590","doi":"10.1038/ng.568","title":"New loci associated with kidney function and chronic kidney disease","year":2010,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Renal Diseases and Glomerulopathies","field":"Medicine","cited_by":810,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"McMaster University","funders":"National Institute of Dental and Craniofacial Research; National Center for Research Resources; National Institute of General Medical Sciences; National Human Genome Research Institute; National Institute of Diabetes and Digestive and Kidney Diseases; National Heart, Lung, and Blood Institute; National Institute on Aging","keywords":"Biology; Kidney disease; Renal function; Cystatin C; Genome-wide association study; Creatinine; Population; Genetics; Kidney; Internal medicine; Endocrinology; Bioinformatics; Genotype; Single-nucleotide polymorphism; Gene; Medicine","score_opus":0.004292497832546768,"score_gpt":0.23285133265144706,"score_spread":0.2285588348189003,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2165019590","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.98103666,0.003921639,0.005449977,0.0024571635,0.00041201597,0.000033729048,0.0010519159,0.00012386523,0.005513081],"genre_scores_gemma":[0.99024487,0.0010022819,0.004069776,0.0005303697,0.0006676064,0.000023065206,0.0005709001,0.00006462353,0.0028265864],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99891424,0.00025469976,0.00012016601,0.00031651556,0.00026202004,0.00013237701],"domain_scores_gemma":[0.9972727,0.0011771935,0.00070635346,0.00019588557,0.00019981747,0.00044802745],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00070868334,0.0013319004,0.00089840917,0.0022671917,0.00083704933,0.0012627244,0.0012420707,0.0022798262,0.0062726066],"category_scores_gemma":[0.0030316692,0.00050567195,0.0012812141,0.0020734111,0.0007631395,0.0005498077,0.0008452318,0.0013939304,0.00047177184],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.008796755,0.0008962277,0.60245025,0.00053122727,0.0036541251,0.061000492,0.0022337027,0.0033588384,0.23445661,0.012522226,0.0055106278,0.064588964],"study_design_scores_gemma":[0.00079867896,0.0004888943,0.9111408,0.000155604,0.0021343264,0.043956913,0.0006150055,0.0031389643,0.011504905,0.011240645,0.014681755,0.00014348998],"about_ca_topic_score_codex":0.0017495571,"about_ca_topic_score_gemma":0.0021431248,"teacher_disagreement_score":0.0062726066,"about_ca_system_score_codex":0.000428374,"about_ca_system_score_gemma":0.00036268914,"threshold_uncertainty_score":0.020983994},"labels":[],"label_agreement":null},{"id":"W2165872127","doi":"10.1038/ng.175","title":"Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease","year":2008,"lang":"en","type":"review","venue":"Nature Genetics","topic":"Inflammatory Bowel Disease","field":"Biochemistry, Genetics and Molecular Biology","cited_by":2628,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Hospital for Sick Children; McGill University; Mount Sinai Hospital; SickKids Foundation; Royal Victoria Hospital; University of Toronto; Université de Montréal; Montreal Heart Institute","funders":"National Institute of Diabetes and Digestive and Kidney Diseases; National Institute of Allergy and Infectious Diseases; Wellcome Trust","keywords":"Biology; Genome-wide association study; Disease; Genetics; Genome; Genetic association; Crohn's disease; Single-nucleotide polymorphism; Gene; Genotype; Medicine; Internal medicine","score_opus":0.012369590552559095,"score_gpt":0.2866665089245244,"score_spread":0.2742969183719653,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2165872127","genre_codex":"review","genre_gemma":"review","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"review","genre_consensus":"review","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.00042430306,0.9956344,0.000951693,0.0011878121,0.00045232277,0.0000069233342,0.000058485562,0.000025287383,0.001258791],"genre_scores_gemma":[0.001669552,0.9948605,0.0011926045,0.00076598313,0.00058691076,0.0000139106905,0.000101121725,0.0000034153718,0.00080596015],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.9997266,0.000046854533,0.000031154097,0.00006388103,0.000107058164,0.000024501474],"domain_scores_gemma":[0.9994386,0.00028473168,0.00006240788,0.000021365653,0.00013960365,0.000053263895],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0012146784,0.0012227893,0.0021638111,0.0012286747,0.00022845593,0.0011035758,0.0013077697,0.0016930689,0.0018655175],"category_scores_gemma":[0.0009515905,0.00034432873,0.00045274076,0.0018515306,0.0007186154,0.000960988,0.00073954515,0.0019315436,0.0014124411],"study_design_candidate":"not_applicable","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00018379115,0.000049298455,0.0010521427,0.0042099874,0.00017265894,0.00050534384,0.000042498566,0.00038304765,0.003693393,0.0036385118,0.03749358,0.94857585],"study_design_scores_gemma":[0.00011650664,0.00008718358,0.006059742,0.0021283738,0.00037284897,0.0026214458,0.00009877781,0.0001675414,0.0011029254,0.0060490114,0.9811519,0.000043664917],"about_ca_topic_score_codex":0.001203596,"about_ca_topic_score_gemma":0.002746474,"teacher_disagreement_score":0.0021638111,"about_ca_system_score_codex":0.0006137307,"about_ca_system_score_gemma":0.0009847733,"threshold_uncertainty_score":0.00642395},"labels":[],"label_agreement":null},{"id":"W2166483810","doi":"10.1038/ng1765","title":"MPV17 encodes an inner mitochondrial membrane protein and is mutated in infantile hepatic mitochondrial DNA depletion","year":2006,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Mitochondrial Function and Pathology","field":"Biochemistry, Genetics and Molecular Biology","cited_by":418,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Alberta","funders":"Fondazione Telethon; Fondazione Pierfranco e Luisa Mariani; European Commission","keywords":"Biology; Mitochondrial DNA; Locus (genetics); Genetics; Gene; Mitochondrion; Inner mitochondrial membrane; Molecular biology","score_opus":0.004975404654888795,"score_gpt":0.23524072802813373,"score_spread":0.23026532337324493,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2166483810","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99272436,0.0010121514,0.0023554668,0.00042847992,0.00022773405,0.00004609702,0.0012264722,0.00022946396,0.0017498075],"genre_scores_gemma":[0.9964359,0.0003985448,0.0011751418,0.000056159995,0.000047053432,0.000029969826,0.0005939315,0.00008220293,0.0011812261],"study_design_codex":"case_report","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99973255,0.000038194255,0.000048265767,0.000050171227,0.00007505751,0.000055736848],"domain_scores_gemma":[0.99885833,0.00034402666,0.00044246943,0.000050663086,0.000055458946,0.00024896892],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00022092336,0.0013691827,0.0005518177,0.0018098836,0.0005048727,0.00043981842,0.0011106589,0.0016500384,0.0024709278],"category_scores_gemma":[0.0010098668,0.0004191853,0.0005614849,0.00090253353,0.001306144,0.00031342515,0.0007944714,0.0010018169,0.0008616578],"study_design_candidate":"bench_or_experimental","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0015964846,0.00014228234,0.01766273,0.00034662936,0.00020897499,0.5648493,0.00052451453,0.0007513087,0.39990604,0.0012414766,0.0014719425,0.011298262],"study_design_scores_gemma":[0.0002332052,0.0004969823,0.06489774,0.00012162338,0.00037165056,0.59894174,0.00056965393,0.00220359,0.31873947,0.0011881877,0.012143204,0.00009295195],"about_ca_topic_score_codex":0.001374489,"about_ca_topic_score_gemma":0.00078471453,"teacher_disagreement_score":0.0024709278,"about_ca_system_score_codex":0.0004504916,"about_ca_system_score_gemma":0.00034342898,"threshold_uncertainty_score":0.008266091},"labels":[],"label_agreement":null},{"id":"W2167064895","doi":"10.1038/ng.1105","title":"Heterozygous missense mutations in SMARCA2 cause Nicolaides-Baraitser syndrome","year":2012,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Chromatin Remodeling and Cancer","field":"Biochemistry, Genetics and Molecular Biology","cited_by":244,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Children's Hospital of Eastern Ontario","funders":"","keywords":"Biology; Genetics; Missense mutation; Chromatin remodeling; Exome sequencing; Transcription factor; SMARCA4; Mutation; Gene","score_opus":0.011137291797014228,"score_gpt":0.28337899147193285,"score_spread":0.2722416996749186,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2167064895","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9902734,0.0013455616,0.0023188898,0.00051335467,0.00014166324,0.000032892316,0.00032938793,0.00023248674,0.004812273],"genre_scores_gemma":[0.9974228,0.00025624933,0.0010676598,0.00007490596,0.000083023086,0.000015032742,0.000106624386,0.00003327687,0.0009405578],"study_design_codex":"case_report","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99963593,0.000042862666,0.000047231522,0.000097145785,0.00012842874,0.00004843946],"domain_scores_gemma":[0.99935275,0.00021474522,0.00022430155,0.000030346737,0.00002921734,0.00014865692],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0002192509,0.0019787448,0.00064291584,0.0016881131,0.0006625187,0.0004722578,0.0008320176,0.0025423393,0.002640633],"category_scores_gemma":[0.0011415461,0.00048329227,0.0004730298,0.0011461753,0.0010180401,0.00036241795,0.0006958857,0.00066714466,0.00082387193],"study_design_candidate":"bench_or_experimental","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00069235667,0.000105895924,0.02645542,0.00013650849,0.00022439276,0.75753856,0.00057446497,0.0009831156,0.2016307,0.0014408487,0.001568328,0.008649398],"study_design_scores_gemma":[0.00022082095,0.00024981736,0.06649651,0.000055496723,0.00054560596,0.8504547,0.00040378427,0.00351369,0.068332374,0.0010849714,0.008566214,0.00007595949],"about_ca_topic_score_codex":0.001122978,"about_ca_topic_score_gemma":0.001468619,"teacher_disagreement_score":0.002640633,"about_ca_system_score_codex":0.0005441671,"about_ca_system_score_gemma":0.00028558762,"threshold_uncertainty_score":0.008833826},"labels":[],"label_agreement":null},{"id":"W2167398354","doi":"10.1038/ng1640","title":"The synthetic genetic interaction spectrum of essential genes","year":2005,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Fungal and yeast genetics research","field":"Biochemistry, Genetics and Molecular Biology","cited_by":225,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Canada Research Chairs; University of Toronto","funders":"","keywords":"Biology; Gene; Genetics; Mutant; Yeast; Computational biology; Genetic screen","score_opus":0.00521645381536995,"score_gpt":0.2787987811037856,"score_spread":0.27358232728841564,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2167398354","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.92009455,0.0017026952,0.05104083,0.00059475086,0.000088846515,0.00003950568,0.00064492185,0.0012990237,0.02449482],"genre_scores_gemma":[0.9897254,0.0007104762,0.006157869,0.0001913764,0.000030433726,0.000029689463,0.00065639726,0.0001804934,0.0023177648],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.999608,0.000058857346,0.00001861811,0.00007617157,0.0001776101,0.000060841732],"domain_scores_gemma":[0.9992884,0.00031349095,0.00007518045,0.00012936856,0.00005222194,0.00014148052],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00033639898,0.0007121599,0.00032493638,0.0007313451,0.00024178358,0.0005095845,0.00040846402,0.00039615086,0.0033669823],"category_scores_gemma":[0.000746726,0.00024085818,0.00030953152,0.00025738776,0.00035471353,0.00052265334,0.00091836683,0.0009505217,0.0007030272],"study_design_candidate":"bench_or_experimental","study_design_consensus":"bench_or_experimental","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0001943749,0.000024249905,0.0002748667,0.00002779682,0.000010704014,0.000099455996,0.000009618002,0.0004342489,0.9877864,0.004758876,0.0001567116,0.0062225983],"study_design_scores_gemma":[0.000047136273,0.00035730843,0.0051234714,0.000014903918,0.00005202296,0.0027210086,0.000050165534,0.0067786574,0.963971,0.011048502,0.0098088775,0.000026928994],"about_ca_topic_score_codex":0.000108040185,"about_ca_topic_score_gemma":0.00014014028,"teacher_disagreement_score":0.0033669823,"about_ca_system_score_codex":0.00035391384,"about_ca_system_score_gemma":0.00017608725,"threshold_uncertainty_score":0.011263669},"labels":[],"label_agreement":null},{"id":"W2167557855","doi":"10.1038/ng1276","title":"Mutations in ARFGEF2 implicate vesicle trafficking in neural progenitor proliferation and migration in the human cerebral cortex","year":2003,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Neurogenesis and neuroplasticity mechanisms","field":"Neuroscience","cited_by":390,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Université de Sherbrooke; Hôpital Fleurimont","funders":"McKnight Foundation; March of Dimes Foundation; National Institute of Mental Health; Massachusetts Institute of Technology; Howard Hughes Medical Institute","keywords":"Biology; Cell biology; Golgi apparatus; Cerebral cortex; Brefeldin A; In situ hybridization; Neural stem cell; Molecular biology; Gene expression; Neuroscience; Genetics; Gene; Stem cell","score_opus":0.024989565069877488,"score_gpt":0.283292461909029,"score_spread":0.25830289683915153,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2167557855","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99573934,0.00081859983,0.001714745,0.00020842001,0.000025973872,0.0000062833997,0.0001280696,0.000067062756,0.0012915084],"genre_scores_gemma":[0.99829644,0.00022129506,0.0004923541,0.000033888442,0.000011763169,0.0000057778025,0.0000772785,0.000021149224,0.00083999825],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9998776,0.000020168212,0.000011635457,0.000029251005,0.000032355005,0.00002901579],"domain_scores_gemma":[0.9998746,0.000036832644,0.000035009263,0.000012834962,0.000009647346,0.000031084033],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00014281823,0.00047471377,0.00033358487,0.00045979983,0.000478168,0.00050062855,0.00023305607,0.0009117615,0.0013315768],"category_scores_gemma":[0.00031273713,0.0002868645,0.0003074378,0.00019144536,0.0006671431,0.00028953853,0.00036799032,0.00058825855,0.0003565596],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00064495986,0.00004673562,0.006230537,0.000070106704,0.000064969325,0.007235149,0.00018401173,0.0011032722,0.973096,0.0028180915,0.00059886725,0.00790731],"study_design_scores_gemma":[0.00016471083,0.00023397585,0.1267509,0.000049848553,0.0003102412,0.058602493,0.0005514021,0.0077779847,0.7894371,0.0040325206,0.012020184,0.00006866771],"about_ca_topic_score_codex":0.0014880961,"about_ca_topic_score_gemma":0.0017695599,"teacher_disagreement_score":0.0014880961,"about_ca_system_score_codex":0.00032980228,"about_ca_system_score_gemma":0.00029166468,"threshold_uncertainty_score":0.004454553},"labels":[],"label_agreement":null},{"id":"W2168272873","doi":"10.1038/ng2089","title":"Genome-wide association scan identifies a colorectal cancer susceptibility locus on chromosome 8q24","year":2007,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Genetic factors in colorectal cancer","field":"Medicine","cited_by":730,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Ontario Institute for Cancer Research; Memorial University of Newfoundland; Hospital for Sick Children; McGill University and Génome Québec Innovation Centre; University of Toronto; Lunenfeld-Tanenbaum Research Institute; Mount Sinai Hospital; Cancer Care Ontario","funders":"National Cancer Institute","keywords":"Locus (genetics); Biology; Genetics; Single-nucleotide polymorphism; Odds ratio; Genome-wide association study; Genetic association; Colorectal cancer; Confidence interval; Genotype; Internal medicine; Gene; Cancer; Medicine","score_opus":0.009959749934661194,"score_gpt":0.29167000372583984,"score_spread":0.28171025379117864,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2168272873","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99585754,0.0009802395,0.0008519591,0.0006416847,0.000047832364,0.000012189129,0.0005609222,0.00006904802,0.0009785657],"genre_scores_gemma":[0.99730766,0.00030902823,0.0010540278,0.000111985384,0.000058545764,0.000012928999,0.000426415,0.000013973477,0.0007055071],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99963546,0.000088484936,0.000026712201,0.00010720001,0.000087962195,0.000054176486],"domain_scores_gemma":[0.9988311,0.0005455203,0.00027912582,0.00005166944,0.00010001635,0.00019264613],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00048262332,0.0005697129,0.0005965974,0.0022552803,0.0007539888,0.00050407666,0.0008589251,0.0011103854,0.0055593676],"category_scores_gemma":[0.0020369252,0.0003447531,0.0006868885,0.0016167699,0.0005089018,0.00020483437,0.00047261783,0.00073189737,0.00038760004],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0064610397,0.0004321184,0.77423024,0.00026860976,0.0020430486,0.018336764,0.00051088753,0.00073952874,0.16146499,0.00081545144,0.004364229,0.030333199],"study_design_scores_gemma":[0.00054451387,0.0005601364,0.9701185,0.00004464338,0.0016025129,0.012744106,0.00031815993,0.0014038511,0.007448928,0.0008485325,0.004331116,0.00003500826],"about_ca_topic_score_codex":0.0040021725,"about_ca_topic_score_gemma":0.0063749473,"teacher_disagreement_score":0.0055593676,"about_ca_system_score_codex":0.000255921,"about_ca_system_score_gemma":0.00032413812,"threshold_uncertainty_score":0.0185979},"labels":[],"label_agreement":null},{"id":"W2169157966","doi":"10.1038/ng.1084","title":"Mutations in CTC1, encoding conserved telomere maintenance component 1, cause Coats plus","year":2012,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Telomeres, Telomerase, and Senescence","field":"Medicine","cited_by":291,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Alberta Children's Hospital; Mount Sinai Hospital; SickKids Foundation; Hospital for Sick Children; University of Toronto","funders":"Great Ormond Street Hospital Charity; National Heart, Lung, and Blood Institute; National Institute for Health and Care Research; Newlife the Charity for Disabled Children","keywords":"Biology; Telomere; Dyskeratosis congenita; Genetics; Telomere-binding protein; Mutation; DNA replication; Cell biology; Arabidopsis; Mutant; DNA; Gene; DNA-binding protein; Transcription factor","score_opus":0.031463180624848076,"score_gpt":0.30412243672927286,"score_spread":0.27265925610442476,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2169157966","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.97829163,0.0009767864,0.0077165035,0.0009852964,0.0007410906,0.00015749806,0.0018204349,0.0012916545,0.008019178],"genre_scores_gemma":[0.99188155,0.00023947362,0.0025950442,0.0001735217,0.00012347531,0.000022836191,0.0005671147,0.00024278567,0.004154334],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9995857,0.00003783055,0.000037862053,0.000113938935,0.00017339284,0.000051225892],"domain_scores_gemma":[0.998166,0.00042430562,0.00057424704,0.00009818551,0.00008686535,0.0006503901],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00025361223,0.00224453,0.00046167936,0.0017296828,0.0010988561,0.0005724694,0.00068767613,0.0016403478,0.005017097],"category_scores_gemma":[0.0009908278,0.00036831916,0.0006349037,0.00077058794,0.0012475466,0.0002474628,0.0010361528,0.0015005593,0.00087062625],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0014539672,0.0003124488,0.0073632263,0.0002366639,0.00023791463,0.060493235,0.00028307165,0.0010232654,0.90852654,0.0034082755,0.005719462,0.010941882],"study_design_scores_gemma":[0.0010314011,0.0012891409,0.14346075,0.00012616094,0.0007550604,0.29291913,0.00037259172,0.019035004,0.49143785,0.0040705777,0.045174714,0.00032754565],"about_ca_topic_score_codex":0.004470561,"about_ca_topic_score_gemma":0.003657293,"teacher_disagreement_score":0.005017097,"about_ca_system_score_codex":0.0009005625,"about_ca_system_score_gemma":0.00062909216,"threshold_uncertainty_score":0.016783893},"labels":[],"label_agreement":null},{"id":"W2169903102","doi":"10.1038/ng1834","title":"CpG island methylator phenotype underlies sporadic microsatellite instability and is tightly associated with BRAF mutation in colorectal cancer","year":2006,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Genetic factors in colorectal cancer","field":"Medicine","cited_by":1985,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"McGill University","funders":"National Cancer Institute; National Institutes of Health","keywords":"MLH1; Microsatellite instability; Biology; DNA methylation; CpG site; Colorectal cancer; Cancer research; Methylation; Genetics; Gene silencing; DNA mismatch repair; Cancer; Microsatellite; Gene; Allele; Gene expression","score_opus":0.007945888930148559,"score_gpt":0.26050186415539733,"score_spread":0.25255597522524875,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2169903102","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9988927,0.00019264994,0.000371795,0.00004387741,0.000008069195,0.000005620349,0.00010259193,0.000024235986,0.00035841909],"genre_scores_gemma":[0.99959725,0.00004797386,0.00015607836,0.000010807061,0.000010655374,0.0000024291655,0.000050527517,0.0000063186058,0.00011798682],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9997291,0.0000560052,0.000033282133,0.000058962687,0.000076829056,0.00004583977],"domain_scores_gemma":[0.99892884,0.00020889647,0.00055773155,0.00006474082,0.00007382882,0.00016594194],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00021936675,0.00032164992,0.00034749435,0.0014918178,0.00032290316,0.00022412493,0.00044304147,0.0005027362,0.001916594],"category_scores_gemma":[0.0012246153,0.00026234236,0.0002104169,0.0007558805,0.00035689474,0.0001533862,0.00035732237,0.00034903458,0.00025286063],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.001949825,0.00016994646,0.46347457,0.00011224176,0.00029593063,0.010478321,0.00028558203,0.00040938877,0.51331216,0.00064443005,0.00051545625,0.008352241],"study_design_scores_gemma":[0.000038129892,0.00032226346,0.9575568,0.000009526248,0.00015091484,0.02244213,0.00014219059,0.0011048671,0.0169957,0.00043520922,0.0007779132,0.000024255703],"about_ca_topic_score_codex":0.0014622763,"about_ca_topic_score_gemma":0.0019100386,"teacher_disagreement_score":0.001916594,"about_ca_system_score_codex":0.00016989833,"about_ca_system_score_gemma":0.00017522152,"threshold_uncertainty_score":0.006411612},"labels":[],"label_agreement":null},{"id":"W2170120898","doi":"10.1038/ng.3274","title":"Genetic conflict reflected in tissue-specific maps of genomic imprinting in human and mouse","year":2015,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":230,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Toronto","funders":"National Institute on Drug Abuse; National Human Genome Research Institute; National Institute of General Medical Sciences; National Institute of Mental Health; National Heart, Lung, and Blood Institute; National Cancer Institute; National Institutes of Health","keywords":"Genomic imprinting; Imprinting (psychology); Biology; Epigenetics; Genetics; Gene; Gene expression; DNA methylation","score_opus":0.01847355808492379,"score_gpt":0.2810012463782578,"score_spread":0.262527688293334,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2170120898","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99417615,0.00070685864,0.0024835705,0.00008259398,0.000012900553,0.000004744409,0.00022138313,0.00004657161,0.002265134],"genre_scores_gemma":[0.99810165,0.00015764082,0.0006605868,0.000034156168,0.000003909992,0.000006275104,0.0001697164,0.000021546832,0.000844559],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9995346,0.00010348699,0.000043047734,0.0001266343,0.00011722497,0.00007508725],"domain_scores_gemma":[0.9993767,0.00023035594,0.00015953399,0.00011392413,0.000037183767,0.00008233537],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0003942038,0.00023315962,0.0003199461,0.0010455701,0.0002513461,0.0007604043,0.0005340475,0.0003917063,0.0026421002],"category_scores_gemma":[0.0007632723,0.00039755326,0.0002626051,0.000427145,0.0007343317,0.00029772418,0.000705423,0.00052958645,0.00025937948],"study_design_candidate":"bench_or_experimental","study_design_consensus":"bench_or_experimental","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0004497515,0.000011787519,0.0034514768,0.000029134073,0.000040515137,0.0003377345,0.00013379415,0.0003029275,0.9884642,0.004286688,0.000058557904,0.0024334828],"study_design_scores_gemma":[0.00010205987,0.00040379722,0.14985801,0.000032855572,0.00019548167,0.008154604,0.0005022643,0.0019968532,0.8266725,0.005708583,0.006327648,0.000045224697],"about_ca_topic_score_codex":0.00065581256,"about_ca_topic_score_gemma":0.00075725577,"teacher_disagreement_score":0.0026421002,"about_ca_system_score_codex":0.00023218596,"about_ca_system_score_gemma":0.00018318763,"threshold_uncertainty_score":0.008838713},"labels":[],"label_agreement":null},{"id":"W2170326618","doi":"10.1038/ng.622","title":"Genome-wide association study identifies a sequence variant within the DAB2IP gene conferring susceptibility to abdominal aortic aneurysm","year":2010,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Aortic aneurysm repair treatments","field":"Medicine","cited_by":217,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Ottawa; Ottawa Hospital","funders":"National Center for Research Resources; National Center for Advancing Translational Sciences; National Institute of Neurological Disorders and Stroke; Eunice Kennedy Shriver National Institute of Child Health and Human Development; National Heart, Lung, and Blood Institute","keywords":"Abdominal aortic aneurysm; Biology; Odds ratio; Aneurysm; Internal medicine; Genome-wide association study; Myocardial infarction; Vascular disease; Aortic aneurysm; Disease; Cardiology; Gene; Medicine; Genetics; Aorta; Single-nucleotide polymorphism; Surgery; Genotype","score_opus":0.015770506633723407,"score_gpt":0.2990853046391739,"score_spread":0.28331479800545045,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2170326618","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9977685,0.00030980026,0.0007672217,0.00016001385,0.000040899544,0.000010158667,0.00019608,0.000017512371,0.0007296968],"genre_scores_gemma":[0.9992305,0.00007528177,0.0003196921,0.000045943183,0.000033314744,0.000003811347,0.000103878156,0.000007108043,0.00018043768],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99947757,0.00016580461,0.000058921494,0.00014829909,0.00008298659,0.00006638389],"domain_scores_gemma":[0.99901414,0.00043962421,0.00020406507,0.000076816286,0.00007175932,0.00019343742],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0005158001,0.00078671257,0.0005086166,0.0012111206,0.0007470652,0.0005826462,0.0005699967,0.0011366507,0.0021885794],"category_scores_gemma":[0.0013605264,0.00033362623,0.0007366419,0.0012902699,0.00062175654,0.00019758345,0.00036494722,0.0012787812,0.00028222264],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0072178165,0.00055303064,0.7814301,0.0001321693,0.0021486436,0.019785237,0.00062520214,0.00066239614,0.17699368,0.00078207976,0.00094827515,0.008721182],"study_design_scores_gemma":[0.00022568721,0.00040035407,0.97966367,0.00002044324,0.00097480655,0.011792422,0.000244944,0.0014493732,0.004049422,0.00036995183,0.00077698566,0.000031969717],"about_ca_topic_score_codex":0.0028903629,"about_ca_topic_score_gemma":0.0025799924,"teacher_disagreement_score":0.0028903629,"about_ca_system_score_codex":0.00017916133,"about_ca_system_score_gemma":0.00022929891,"threshold_uncertainty_score":0.007321596},"labels":[],"label_agreement":null},{"id":"W2170559900","doi":"10.1038/ng.179","title":"Loss of Fat4 disrupts PCP signaling and oriented cell division and leads to cystic kidney disease","year":2008,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Genetic and Kidney Cyst Diseases","field":"Biochemistry, Genetics and Molecular Biology","cited_by":514,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Toronto; Hospital for Sick Children; Mount Sinai Hospital; St. Michael's Hospital; Lunenfeld-Tanenbaum Research Institute","funders":"Cancer Research UK; PKD Foundation","keywords":"Biology; Frizzled; Cell biology; Transcription factor; Genetics; RNA interference; Signal transduction; Wnt signaling pathway; Gene; RNA","score_opus":0.004990224278685443,"score_gpt":0.2373025494928039,"score_spread":0.23231232521411846,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2170559900","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9838541,0.00084115576,0.008068467,0.0009019199,0.00025643237,0.0000617874,0.0016769958,0.0005153261,0.003823785],"genre_scores_gemma":[0.9879489,0.00051256863,0.004245764,0.00019255304,0.00003305183,0.000050573562,0.00066450186,0.00029316457,0.0060588233],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99936384,0.00011022436,0.00008510155,0.000097701806,0.00022188605,0.00012133043],"domain_scores_gemma":[0.9989986,0.00027333674,0.0002781967,0.000089774185,0.00005020243,0.0003098487],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00037475597,0.0009986926,0.0006245902,0.0018446065,0.00074849644,0.00088854635,0.0012545175,0.0015043296,0.0056279297],"category_scores_gemma":[0.0005429729,0.00074174406,0.0007648851,0.0007106409,0.0017694809,0.00048134863,0.0010555675,0.0019942655,0.001373656],"study_design_candidate":"bench_or_experimental","study_design_consensus":"bench_or_experimental","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00048802263,0.00010267485,0.00048451163,0.000056914923,0.000046683985,0.0012328746,0.000034315268,0.0007582739,0.99370897,0.0012313001,0.00024193006,0.0016135047],"study_design_scores_gemma":[0.00015848546,0.00011170845,0.003534967,0.000018658013,0.000065969354,0.0027138693,0.00011426465,0.0042539034,0.9849348,0.0004940893,0.0035702956,0.000028994633],"about_ca_topic_score_codex":0.003425877,"about_ca_topic_score_gemma":0.0040346943,"teacher_disagreement_score":0.0056279297,"about_ca_system_score_codex":0.0011650737,"about_ca_system_score_gemma":0.0009827259,"threshold_uncertainty_score":0.01882732},"labels":[],"label_agreement":null},{"id":"W2170634666","doi":"10.1038/ng.286","title":"DNA methylation profiles in monozygotic and dizygotic twins","year":2009,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Epigenetics and DNA Methylation","field":"Biochemistry, Genetics and Molecular Biology","cited_by":670,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University Health Network; University of Toronto; Centre for Addiction and Mental Health","funders":"Canadian Institutes of Health Research; National Institutes of Health; National Institute of Mental Health; National Alliance for Research on Schizophrenia and Depression","keywords":"Biology; DNA methylation; Epigenetics; Genetics; Monozygotic twin; CpG site; Buccal swab; Epigenomics; Twin study; Heritability; Gene; Gene expression","score_opus":0.0073573037862918605,"score_gpt":0.2684199468283932,"score_spread":0.26106264304210136,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2170634666","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9993937,0.000103316896,0.00007804587,0.000009939154,0.0000046955015,0.000002930858,0.00016115869,0.000001802035,0.00024447357],"genre_scores_gemma":[0.99828315,0.000116390875,0.00017429984,0.00002330085,0.0000032118655,0.0000072379885,0.00029680718,0.000007834818,0.0010878339],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9997054,0.00007235134,0.000028533523,0.00008072083,0.000061307175,0.00005175922],"domain_scores_gemma":[0.99951315,0.00011077166,0.000075307595,0.000056554996,0.00009158761,0.00015263735],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0002660098,0.00017379154,0.0003721767,0.0012000924,0.00040819214,0.00045041795,0.0002784448,0.00037407543,0.0015155814],"category_scores_gemma":[0.0017903851,0.00024274843,0.00024285536,0.000625237,0.0001970155,0.00009926152,0.0004642199,0.00035826926,0.0002571371],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0059508183,0.00027011012,0.600831,0.000096259304,0.0005050182,0.0013667844,0.004358691,0.00016682076,0.36878166,0.00081835233,0.00049348397,0.016360965],"study_design_scores_gemma":[0.000031274154,0.00035202826,0.98155874,0.000011074383,0.00016881789,0.0033707197,0.0009796391,0.00033224703,0.012139579,0.0002661743,0.00077077694,0.000019007923],"about_ca_topic_score_codex":0.005083147,"about_ca_topic_score_gemma":0.0041923583,"teacher_disagreement_score":0.005083147,"about_ca_system_score_codex":0.00023375708,"about_ca_system_score_gemma":0.00015298699,"threshold_uncertainty_score":0.0101071},"labels":[],"label_agreement":null},{"id":"W2171100097","doi":"10.1038/ng1868","title":"DMP1 mutations in autosomal recessive hypophosphatemia implicate a bone matrix protein in the regulation of phosphate homeostasis","year":2006,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Parathyroid Disorders and Treatments","field":"Medicine","cited_by":526,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Shriners Hospitals for Children - Canada; Queen Elizabeth II Health Sciences Centre","funders":"National Institute of Diabetes and Digestive and Kidney Diseases","keywords":"Hypophosphatemia; DMP1; PHEX; Biology; Endocrinology; Fibroblast growth factor 23; Mutation; Homeostasis; Internal medicine; Sclerostin; Gene; Genetics; Viral matrix protein; Rickets; Parathyroid hormone; Calcium","score_opus":0.00804349083604327,"score_gpt":0.28425328193019167,"score_spread":0.2762097910941484,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2171100097","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.98547137,0.0036433968,0.0052673924,0.00079695304,0.00009544012,0.000020000412,0.00033893753,0.00014117837,0.004225417],"genre_scores_gemma":[0.99602425,0.0006110214,0.0021403518,0.00008859962,0.0000252486,0.000008891997,0.000115717245,0.00002172592,0.00096417475],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.99983346,0.000022468279,0.000017985682,0.000036458,0.000069734146,0.000019897478],"domain_scores_gemma":[0.99974746,0.000097553806,0.000083490835,0.000011632068,0.0000192284,0.00004060424],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00018158267,0.00075594033,0.0003141524,0.00074641866,0.00034655942,0.00041570593,0.0004560511,0.0011468891,0.0022464176],"category_scores_gemma":[0.00062710076,0.00027002234,0.00022889546,0.00032386262,0.000649514,0.00023435694,0.0004362689,0.00089567027,0.00033192892],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0006794863,0.000043760636,0.009343922,0.00014971539,0.00006128629,0.029942041,0.00017293445,0.00058189506,0.9432111,0.003432716,0.00084992027,0.011531212],"study_design_scores_gemma":[0.00027984628,0.00035397327,0.07281735,0.00008948369,0.00023088904,0.18693843,0.00024600627,0.006295034,0.7141514,0.0052410364,0.013308175,0.000048461538],"about_ca_topic_score_codex":0.00090275065,"about_ca_topic_score_gemma":0.00088760065,"teacher_disagreement_score":0.0022464176,"about_ca_system_score_codex":0.00043597538,"about_ca_system_score_gemma":0.00022452424,"threshold_uncertainty_score":0.007515013},"labels":[],"label_agreement":null},{"id":"W2177538943","doi":"10.1038/ng.3437","title":"Genetic fine mapping and genomic annotation defines causal mechanisms at type 2 diabetes susceptibility loci","year":2015,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Genetic Associations and Epidemiology","field":"Biochemistry, Genetics and Molecular Biology","cited_by":424,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"McGill University and Génome Québec Innovation Centre; Centre Hospitalier de l’Université de Montréal","funders":"National Institute on Aging; Medical Research Council; U.S. Public Health Service; National Institutes of Health; Heinz Nixdorf Stiftung; H. Lundbeck A/S; National Center for Research Resources; Diabetesliitto; Deutsche Forschungsgemeinschaft; Svenska Läkaresällskapet; Novo Nordisk Fonden; Hjerteforeningen; Magnus Bergvalls Stiftelse; Opetus- ja Kulttuuriministeriö; Sydäntutkimussäätiö; Augustinus Fonden; National Human Genome Research Institute; Danmarks Frie Forskningsfond; Vetenskapsrådet; Stockholms Läns Landsting; Royal Swedish Academy of Sciences; Diabetes UK; Etelä-Pohjanmaan Sairaanhoitopiiri; Signe ja Ane Gyllenbergin Säätiö; Kuopion Yliopistollinen Sairaala; National Institute of Diabetes and Digestive and Kidney Diseases; Norwegian Institute of Public Health; Stiftelsen för Gamla Tjänarinnor; Helsingin ja Uudenmaan Sairaanhoitopiiri; Knut och Alice Wallenbergs Stiftelse; Paavo Nurmen Säätiö; Novo Nordisk; Hjärt-Lungfonden; Foundation for Cardiovascular Research; Pirkanmaan Sairaanhoitopiiri; Finska Läkaresällskapet; National Cancer Institute; Lundbeckfonden; National Heart, Lung, and Blood Institute; Bundesministerium für Gesundheit; School of Medicine, Boston University; European Commission; British Heart Foundation; Bundesministerium für Bildung und Forschung; Varsinais-Suomen Sairaanhoitopiiri; National Institute for Health and Care Research; Swedish e-Science Research Centre; Norges Forskningsråd; Stiftelsen för Strategisk Forskning; Erasmus Medisch Centrum; Helmholtz Zentrum München; Kela; ZonMw; Diabetestutkimussäätiö; Wellcome Trust; Karolinska Institutet; European Regional Development Fund; Terveyden ja hyvinvoinnin laitos","keywords":"Biology; Genetics; Annotation; Type 2 diabetes; Computational biology; Genome-wide association study; Evolutionary biology; Single-nucleotide polymorphism; Diabetes mellitus; Genotype; Gene","score_opus":0.014848158334294962,"score_gpt":0.25402163858151006,"score_spread":0.2391734802472151,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2177538943","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9480967,0.0027691855,0.03818019,0.0011349806,0.00019514811,0.00006418091,0.004027577,0.00035194797,0.0051800613],"genre_scores_gemma":[0.9752319,0.0010357045,0.01877734,0.0004687183,0.00015605915,0.000052259962,0.0024424766,0.00014297826,0.0016926014],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.99901307,0.00026802366,0.00008464761,0.00033431943,0.00017083835,0.00012895359],"domain_scores_gemma":[0.9972186,0.0015131144,0.0005082388,0.0004079026,0.00014648728,0.00020567316],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0013957907,0.0006619447,0.0005630922,0.0032708817,0.0007167336,0.0014855136,0.0010220055,0.0010532556,0.0045238794],"category_scores_gemma":[0.002733225,0.0005628309,0.0011542063,0.0023136619,0.00063209626,0.00050159055,0.00108152,0.0014214591,0.0006322535],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0030975111,0.0006313522,0.41891888,0.00069849804,0.0015839991,0.0052805156,0.0012660384,0.003567137,0.439108,0.016150648,0.0029806008,0.10671683],"study_design_scores_gemma":[0.00047557935,0.00027029583,0.875628,0.00025390225,0.0019435945,0.0044818292,0.00076126703,0.0077272705,0.054658677,0.031041218,0.022632662,0.00012572059],"about_ca_topic_score_codex":0.002105666,"about_ca_topic_score_gemma":0.0033131328,"teacher_disagreement_score":0.0045238794,"about_ca_system_score_codex":0.0003420532,"about_ca_system_score_gemma":0.00041946094,"threshold_uncertainty_score":0.015133858},"labels":[],"label_agreement":null},{"id":"W2178552215","doi":"10.1038/ng.3435","title":"The pineapple genome and the evolution of CAM photosynthesis","year":2015,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Photosynthetic Processes and Mechanisms","field":"Biochemistry, Genetics and Molecular Biology","cited_by":734,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Ottawa","funders":"National Human Genome Research Institute; University of Illinois at Urbana-Champaign; Office of Science; U.S. Department of Agriculture; U.S. Department of Energy; National Science Foundation; National Institutes of Health; Fujian Agriculture and Forestry University","keywords":"Ananas; Crassulacean acid metabolism; Biology; Genome; Gene; Circadian clock; Gene duplication; Neofunctionalization; Functional divergence; Genetics; Photosynthesis; Gene family; Botany","score_opus":0.005031207141702419,"score_gpt":0.22133728947464718,"score_spread":0.21630608233294477,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2178552215","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.94389814,0.034142207,0.0043240334,0.003043355,0.00038785365,0.000015739135,0.0012375534,0.0003397428,0.012611318],"genre_scores_gemma":[0.9834289,0.0066485824,0.0034360357,0.0007854831,0.000120394565,0.000005500751,0.0012886911,0.00003726869,0.0042490843],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9999331,0.0000050727876,0.0000025250395,0.000027814787,0.000018775681,0.000012615016],"domain_scores_gemma":[0.99989104,0.000019728526,0.000028862842,0.000010103115,0.00002018155,0.000030106057],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00013315018,0.0002208806,0.00011101748,0.0002351894,0.00028914624,0.0007347489,0.00019449538,0.00037077238,0.0007449144],"category_scores_gemma":[0.00019018217,0.00009074691,0.00013475883,0.00025955637,0.00018738121,0.00031433903,0.00023756664,0.00047543604,0.0002348374],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00044403403,0.000034976645,0.01635266,0.0002822748,0.00005930631,0.0016202717,0.0007832413,0.0007141406,0.87313926,0.005996624,0.0037716983,0.09680142],"study_design_scores_gemma":[0.000051590232,0.0002447388,0.4143974,0.00017176093,0.0001882604,0.0031381254,0.0014219827,0.0026274535,0.20264253,0.010460486,0.3645591,0.000096644464],"about_ca_topic_score_codex":0.0029510988,"about_ca_topic_score_gemma":0.0040028817,"teacher_disagreement_score":0.0029510988,"about_ca_system_score_codex":0.0004336968,"about_ca_system_score_gemma":0.0002998804,"threshold_uncertainty_score":0.005867839},"labels":[],"label_agreement":null},{"id":"W2188122643","doi":"10.1038/ng.3453","title":"Diabetes in the post-GWAS era","year":2015,"lang":"en","type":"letter","venue":"Nature Genetics","topic":"Diabetes and associated disorders","field":"Biochemistry, Genetics and Molecular Biology","cited_by":11,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"McGill University Health Centre","funders":"","keywords":"Biology; Genome-wide association study; Imputation (statistics); Trait; Computational biology; Chromatin; Quantitative trait locus; Genetics; Evolutionary biology; Gene; Single-nucleotide polymorphism; Computer science; Machine learning; Genotype","score_opus":0.004588891207900747,"score_gpt":0.2251104853662392,"score_spread":0.22052159415833847,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2188122643","genre_codex":"commentary","genre_gemma":"commentary","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"commentary","genre_consensus":"commentary","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.0004938962,0.0031559584,0.00013324685,0.97257805,0.021976579,0.0000035749108,0.000031684896,0.000015296382,0.0016117544],"genre_scores_gemma":[0.008995182,0.004264907,0.00021768382,0.83542985,0.14751124,0.000014190464,0.000028181517,0.000018646502,0.0035201244],"study_design_codex":"not_applicable","study_design_gemma":"not_applicable","domain_scores_codex":[0.9979261,0.0008143238,0.0002260804,0.00029598575,0.00049033307,0.00024718037],"domain_scores_gemma":[0.9891639,0.0072354306,0.00048323636,0.00045616602,0.0011495941,0.0015117824],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.003735007,0.00054450455,0.001075486,0.00051810144,0.0018379864,0.002592783,0.0009460894,0.02270876,0.005052267],"category_scores_gemma":[0.023299986,0.00035676907,0.0006882482,0.00035853081,0.0027534189,0.003405615,0.0015437779,0.024169173,0.0026502814],"study_design_candidate":"not_applicable","study_design_consensus":"not_applicable","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0002467501,0.00007184159,0.0031269826,0.000103252394,0.000048628906,0.0048875907,0.00011996052,0.000088160945,0.00038379166,0.0093404995,0.9453529,0.03622966],"study_design_scores_gemma":[0.00042410742,0.00017477006,0.006392549,0.0007054783,0.00011517902,0.008178472,0.00047383987,0.0007886964,0.0006075325,0.05043845,0.9315935,0.00010742009],"about_ca_topic_score_codex":0.0018705336,"about_ca_topic_score_gemma":0.0033893918,"teacher_disagreement_score":0.02270876,"about_ca_system_score_codex":0.0021732294,"about_ca_system_score_gemma":0.0014184938,"threshold_uncertainty_score":0.01975286},"labels":[],"label_agreement":null},{"id":"W2194309244","doi":"10.1038/ng.3459","title":"Loss-of-function mutations in TNFAIP3 leading to A20 haploinsufficiency cause an early-onset autoinflammatory disease","year":2015,"lang":"en","type":"article","venue":"Nature Genetics","topic":"NF-κB Signaling Pathways","field":"Biochemistry, Genetics and Molecular Biology","cited_by":633,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"SickKids Foundation; Hospital for Sick Children; University of Toronto","funders":"National Institute of Arthritis and Musculoskeletal and Skin Diseases; NIH Clinical Center; National Institutes of Health; Hacettepe Üniversitesi","keywords":"Haploinsufficiency; Biology; Proinflammatory cytokine; Tumor necrosis factor alpha; Mutation; Immunology; NFKB1; Inflammation; Innate immune system; Cancer research; Penetrance; Deubiquitinating enzyme; NF-κB; Genetics; Ubiquitin; Cell biology; Immune system; Phenotype; Transcription factor; Gene","score_opus":0.02021334091259515,"score_gpt":0.2884948392413314,"score_spread":0.26828149832873627,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2194309244","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9933437,0.0005408717,0.002359463,0.0003038469,0.00009656966,0.000045785553,0.0005806058,0.00022474861,0.0025043546],"genre_scores_gemma":[0.99700123,0.00020025825,0.0012589172,0.00008961041,0.000025871474,0.000011331194,0.00017831597,0.000052143227,0.0011822124],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.99984455,0.000027409558,0.000028541905,0.000028383492,0.00004146839,0.000029646324],"domain_scores_gemma":[0.9995877,0.000118611955,0.0001094706,0.000025044035,0.00002493139,0.00013427208],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00018107505,0.0010361138,0.00039347186,0.000667029,0.0004548281,0.00033975998,0.0003073698,0.0009731316,0.0028400954],"category_scores_gemma":[0.00043008124,0.00021570535,0.00042170513,0.0003694359,0.00051783014,0.0001786702,0.00039284746,0.0007116249,0.0007566704],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00040469997,0.00012557134,0.0043824674,0.00004993826,0.000051915737,0.054880016,0.00009116301,0.00029781315,0.93318325,0.0005969282,0.000537707,0.0053985785],"study_design_scores_gemma":[0.00048567477,0.001212911,0.16112958,0.00007222113,0.000328161,0.32597315,0.00036362058,0.0056856433,0.489517,0.0019975984,0.0131087,0.00012572343],"about_ca_topic_score_codex":0.0007841196,"about_ca_topic_score_gemma":0.0012395491,"teacher_disagreement_score":0.0028400954,"about_ca_system_score_codex":0.00028925764,"about_ca_system_score_gemma":0.00026834593,"threshold_uncertainty_score":0.0095011},"labels":[],"label_agreement":null},{"id":"W2206448631","doi":"10.1038/ng.3366","title":"Pediatric cancer genomics, a play rather than a portrait","year":2015,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Neuroblastoma Research and Treatments","field":"Medicine","cited_by":4,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Hospital for Sick Children","funders":"","keywords":"Biology; Portrait; Genomics; Cancer; Computational biology; Genetics; Bioinformatics; Evolutionary biology; Genome; Gene; Art history","score_opus":0.02296270776851967,"score_gpt":0.32214382262628966,"score_spread":0.29918111485777,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2206448631","genre_codex":"commentary","genre_gemma":"commentary","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"commentary","genre_consensus":"commentary","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.0067951153,0.06585819,0.013986459,0.87817633,0.0106378365,0.000020675161,0.0001998692,0.00017139844,0.024154183],"genre_scores_gemma":[0.2991668,0.15502156,0.03946126,0.4224193,0.05081745,0.0002008761,0.00048937974,0.0008389285,0.031584408],"study_design_codex":"theoretical_or_conceptual","study_design_gemma":"not_applicable","domain_scores_codex":[0.99823666,0.00093974074,0.00010266367,0.0001839987,0.0003915028,0.00014540581],"domain_scores_gemma":[0.99310184,0.004061399,0.00033418715,0.0004887439,0.00081835856,0.001195374],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.009671358,0.0007478665,0.0009891763,0.002164014,0.0027187169,0.0061150733,0.0012742438,0.004440607,0.0039389622],"category_scores_gemma":[0.008854868,0.0005107647,0.00042834668,0.0011979652,0.019332971,0.01793583,0.0032946107,0.015184769,0.0011143591],"study_design_candidate":"not_applicable","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0002643995,0.000082042876,0.0041386266,0.0005605479,0.0000881106,0.0015322072,0.0077926978,0.0007730598,0.0036191128,0.6679811,0.19983757,0.11333052],"study_design_scores_gemma":[0.00008292015,0.00012342924,0.002131513,0.0010082772,0.0000786664,0.003793918,0.010149474,0.00072243967,0.0008896424,0.38086575,0.60007936,0.00007469581],"about_ca_topic_score_codex":0.0024960674,"about_ca_topic_score_gemma":0.004911137,"teacher_disagreement_score":0.009671358,"about_ca_system_score_codex":0.0026630003,"about_ca_system_score_gemma":0.002692166,"threshold_uncertainty_score":0.05114764},"labels":[],"label_agreement":null},{"id":"W2210186672","doi":"10.1038/ng.3443","title":"A supergene determines highly divergent male reproductive morphs in the ruff","year":2015,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Wildlife Ecology and Conservation","field":"Environmental Science","cited_by":586,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Simon Fraser University","funders":"Office of Experimental Program to Stimulate Competitive Research; Natural Environment Research Council; Biotechnology and Biological Sciences Research Council; Medical Research Council; Directorate for Biological Sciences; Simon Fraser University; Natural Sciences and Engineering Research Council of Canada; National Geographic Society; John Simon Guggenheim Memorial Foundation; University of Edinburgh; European Commission; Sight Research UK; National Science Foundation","keywords":"Biology; Supergene (geology); Evolutionary biology; Zoology; Reproduction; Ecology","score_opus":0.015831398996303897,"score_gpt":0.23748768556525085,"score_spread":0.22165628656894695,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2210186672","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9990784,0.00009050044,0.0004677038,0.000014566719,0.0000025930901,0.0000032949729,0.000031913158,0.000006730333,0.00030428683],"genre_scores_gemma":[0.99807644,0.0000760566,0.00085477886,0.00004729078,0.0000064320457,0.000008375898,0.000251707,0.000009922447,0.00066895393],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.99990404,0.000010460664,0.000005135137,0.000030506628,0.00003050849,0.000019311266],"domain_scores_gemma":[0.9998373,0.000048096113,0.00005575577,0.0000086393575,0.000012567003,0.000037672566],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.000087961205,0.00017724062,0.00013552155,0.0006465674,0.0002525857,0.00017672812,0.00019988362,0.00023578147,0.000937103],"category_scores_gemma":[0.00015618684,0.00012096459,0.0001680314,0.00016147218,0.00033544033,0.00009128432,0.00033842,0.00032159992,0.00016571044],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00024384813,0.000039076247,0.032551177,0.000022308353,0.00001979295,0.00063037366,0.00037421007,0.00009711622,0.9568586,0.00054212357,0.000096656826,0.008524657],"study_design_scores_gemma":[0.000060176568,0.00030973967,0.89829224,0.000033681972,0.00007495432,0.006989097,0.0005394805,0.0018064389,0.08572853,0.00054041017,0.005586886,0.000038219445],"about_ca_topic_score_codex":0.0011858885,"about_ca_topic_score_gemma":0.004200564,"teacher_disagreement_score":0.0011858885,"about_ca_system_score_codex":0.00018324231,"about_ca_system_score_gemma":0.00010634203,"threshold_uncertainty_score":0.0031349063},"labels":[],"label_agreement":null},{"id":"W2211416430","doi":"10.1038/ng.3371","title":"The transcriptomic landscape and directed chemical interrogation of MLL-rearranged acute myeloid leukemias","year":2015,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Acute Myeloid Leukemia Research","field":"Medicine","cited_by":170,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Centre hospitalier de l'Université Laval; Hôpital de l'Enfant-Jésus; Institute for Research in Immunology and Cancer; Université Laval; Université de Montréal; Hôpital Maisonneuve-Rosemont","funders":"","keywords":"Biology; Myeloid leukemia; Transcriptome; Fusion gene; Myeloid; Cancer research; Gene; Gene rearrangement; Leukemia; Genetics; Computational biology; Gene expression","score_opus":0.016134963382756225,"score_gpt":0.2926540907233576,"score_spread":0.27651912734060136,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2211416430","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9835579,0.0016188637,0.008104282,0.0003948499,0.000037786394,0.00004273103,0.0025566458,0.00013876287,0.0035481532],"genre_scores_gemma":[0.9859272,0.0011669821,0.007473808,0.00041972386,0.00003269937,0.000054516957,0.002216421,0.000068395886,0.002640188],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99978393,0.000024713083,0.000007060377,0.0000611552,0.00008518662,0.000038002847],"domain_scores_gemma":[0.9998721,0.00003787178,0.000042606956,0.000011052082,0.00002297342,0.000013358504],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0001866227,0.00018982038,0.00015047412,0.00034691312,0.00020981407,0.00051018037,0.00019825432,0.00030187346,0.0012085652],"category_scores_gemma":[0.0003195772,0.00016261154,0.00018348306,0.00028512214,0.00027554354,0.00021179486,0.00022947673,0.00042551287,0.00034859526],"study_design_candidate":"bench_or_experimental","study_design_consensus":"bench_or_experimental","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00006585599,0.000005902946,0.0007115476,0.000025419304,0.0000051410752,0.000024788114,0.00001411871,0.00020669778,0.9970891,0.00018973374,0.000056617693,0.0016051535],"study_design_scores_gemma":[0.000013784279,0.00014643255,0.011098052,0.000007439849,0.000027145043,0.00018481634,0.000110773166,0.0030506959,0.98084027,0.00045067983,0.004061863,0.000008088782],"about_ca_topic_score_codex":0.00039900118,"about_ca_topic_score_gemma":0.0010732055,"teacher_disagreement_score":0.0012085652,"about_ca_system_score_codex":0.00038909426,"about_ca_system_score_gemma":0.00019784586,"threshold_uncertainty_score":0.0040431023},"labels":[],"label_agreement":null},{"id":"W2213548494","doi":"10.1038/ng.3333","title":"Relapsed neuroblastomas show frequent RAS-MAPK pathway mutations","year":2015,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Neuroblastoma Research and Treatments","field":"Medicine","cited_by":555,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Princess Margaret Cancer Centre; University of Toronto","funders":"National Human Genome Research Institute; National Cancer Institute; National Institutes of Health; U.S. Department of Health and Human Services; Universiteit van Amsterdam; Fondation Nelia et Amadeo Barletta; Agence Nationale de la Recherche; National Institute on Minority Health and Health Disparities; Annenberg Foundation","keywords":"Biology; Neuroblastoma; MAPK/ERK pathway; Cancer research; Somatic cell; Phenotype; Mutation; In vivo; Germline mutation; Genotype; Genetics; Cell culture; Signal transduction; Gene","score_opus":0.02693391353906878,"score_gpt":0.3070803402388448,"score_spread":0.280146426699776,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2213548494","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.98447233,0.0023372362,0.0011544477,0.00030646994,0.000055269404,0.000021102423,0.0011040438,0.00021153109,0.010337607],"genre_scores_gemma":[0.9963636,0.00060972926,0.0008916463,0.000055647066,0.000023840514,0.0000070865813,0.00057041255,0.0000374952,0.0014406906],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.99971074,0.000024988782,0.000036407524,0.000060273673,0.00011431674,0.000053359603],"domain_scores_gemma":[0.99955493,0.00008763284,0.00013455085,0.00007124296,0.00008823244,0.000063517386],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0002458458,0.00041581492,0.00040373107,0.0010164048,0.00035250798,0.00065500644,0.00037146828,0.0006710546,0.0040051276],"category_scores_gemma":[0.00076279964,0.00021303132,0.00038777007,0.0009849886,0.0003232848,0.00042268634,0.0004803091,0.00035417068,0.0015465616],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0010170146,0.00007349391,0.31127578,0.00021907357,0.00020723455,0.096483424,0.000631798,0.00061190187,0.52858907,0.0011418213,0.0029946778,0.056754634],"study_design_scores_gemma":[0.00004159268,0.00025571254,0.53856933,0.000054149503,0.00030091134,0.35563704,0.0011207622,0.0009926198,0.08670666,0.0015946378,0.0146806585,0.00004597664],"about_ca_topic_score_codex":0.0015104553,"about_ca_topic_score_gemma":0.0021300663,"teacher_disagreement_score":0.0040051276,"about_ca_system_score_codex":0.00032434615,"about_ca_system_score_gemma":0.00021566382,"threshold_uncertainty_score":0.013398528},"labels":[],"label_agreement":null},{"id":"W2214711630","doi":"10.1038/ng.3360","title":"Analysis of mammalian gene function through broad-based phenotypic screens across a consortium of mouse clinics","year":2015,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Gene expression and cancer classification","field":"Biochemistry, Genetics and Molecular Biology","cited_by":159,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Toronto Centre for Phenogenomics; Hospital for Sick Children; Lunenfeld-Tanenbaum Research Institute; University of Manitoba; Mount Sinai Hospital","funders":"Biotechnology and Biological Sciences Research Council; Medical Research Council; Agence Nationale de la Recherche; Cancer Research UK; Wellcome Trust","keywords":"Biology; Phenotype; Genetics; Gene; Computational biology; Pleiotropy; Gene knockout; Allele; Function (biology)","score_opus":0.0257201222050034,"score_gpt":0.3245867217894223,"score_spread":0.29886659958441886,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2214711630","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.947092,0.0011362745,0.042799767,0.00037417182,0.00003346548,0.00056259375,0.002519373,0.0007889102,0.004693446],"genre_scores_gemma":[0.9445814,0.0018531812,0.041840807,0.0005127399,0.000027135427,0.0009063263,0.0047509777,0.0006579569,0.0048694895],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9978891,0.00042846872,0.00019228723,0.000485036,0.00068803394,0.00031706554],"domain_scores_gemma":[0.99842536,0.00046176108,0.0003105866,0.0002836009,0.00024132288,0.00027737574],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0026718697,0.0007837502,0.0007541487,0.003570399,0.00085600425,0.0010009044,0.0008165233,0.0005692648,0.002974003],"category_scores_gemma":[0.0012463839,0.00041827542,0.00083553954,0.0013946401,0.0007299,0.00040860538,0.0018123282,0.0011613729,0.00051666365],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00017226029,0.00011342564,0.0021037727,0.000030192872,0.000047313697,0.000115622286,0.000051848347,0.00019178941,0.9917317,0.0005096656,0.00018324355,0.004749225],"study_design_scores_gemma":[0.00020694065,0.0014481181,0.07120339,0.000051952014,0.00069384027,0.0039936565,0.00028981842,0.005086729,0.90364665,0.00048159168,0.012835406,0.00006184871],"about_ca_topic_score_codex":0.0027895153,"about_ca_topic_score_gemma":0.008003862,"teacher_disagreement_score":0.003570399,"about_ca_system_score_codex":0.0006069113,"about_ca_system_score_gemma":0.00078429707,"threshold_uncertainty_score":0.014130354},"labels":[],"label_agreement":null},{"id":"W2215458091","doi":"10.1038/ng.3341","title":"Common variation at 2p13.3, 3q29, 7p13 and 17q25.1 associated with susceptibility to pancreatic cancer","year":2015,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Pancreatic and Hepatic Oncology Research","field":"Medicine","cited_by":270,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Public Health Ontario; Cancer Care Ontario; Princess Margaret Cancer Centre; University of Toronto; University Health Network; Lunenfeld-Tanenbaum Research Institute; Mount Sinai Hospital","funders":"National Center for Advancing Translational Sciences; National Cancer Institute; Cancer Research UK; National Institutes of Health; National Center for Chronic Disease Prevention and Health Promotion; National Heart, Lung, and Blood Institute; National Institute for Health and Care Research; World Health Organization","keywords":"Pancreatic cancer; Penetrance; Odds ratio; Biology; PALB2; Cancer; Internal medicine; Confidence interval; Genome-wide association study; Oncology; Genetics; Bioinformatics; Genotype; Mutation; Medicine; Single-nucleotide polymorphism; Gene","score_opus":0.032584871265706736,"score_gpt":0.3574521550864753,"score_spread":0.32486728382076857,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2215458091","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9969728,0.00056597084,0.00061035645,0.0001421758,0.00003144077,0.000019174082,0.0008819612,0.000026228066,0.0007499519],"genre_scores_gemma":[0.9983175,0.00019586334,0.00046366485,0.000040597584,0.00002858378,0.000012274775,0.00053113245,0.000018533208,0.0003918838],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99915123,0.00016025577,0.000108545806,0.00031346644,0.00015460433,0.00011191572],"domain_scores_gemma":[0.9981147,0.0006783205,0.0006615793,0.00012971692,0.00012518755,0.0002906002],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00042951157,0.0008461467,0.00055831496,0.0023589963,0.00057581515,0.0005706191,0.00072445214,0.00091377273,0.0053935284],"category_scores_gemma":[0.001794108,0.0003929403,0.0012534168,0.0027719408,0.0007097567,0.00022271153,0.0006476364,0.0008779424,0.00027975772],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0035712745,0.00016129565,0.8610233,0.00018025277,0.0022314994,0.02215818,0.0010543241,0.0015469644,0.09115543,0.0017716693,0.0013768502,0.013769022],"study_design_scores_gemma":[0.000125533,0.0001621153,0.9818231,0.00006121001,0.0006394869,0.011295466,0.00023012681,0.0007502486,0.0025610917,0.0009947013,0.0013261336,0.000030866802],"about_ca_topic_score_codex":0.008804149,"about_ca_topic_score_gemma":0.008004066,"teacher_disagreement_score":0.008804149,"about_ca_system_score_codex":0.00040747406,"about_ca_system_score_gemma":0.00035915463,"threshold_uncertainty_score":0.01804316},"labels":[],"label_agreement":null},{"id":"W2227148039","doi":"10.1038/ng.3374","title":"A coding variant in RARG confers susceptibility to anthracycline-induced cardiotoxicity in childhood cancer","year":2015,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Chemotherapy-induced cardiotoxicity and mitigation","field":"Medicine","cited_by":275,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Janeway Children's Health and Rehabilitation Centre; McGill University Health Centre; Centre Hospitalier Universitaire Sainte-Justine; Kingston General Hospital; McMaster Children's Hospital; London Health Sciences Centre; Health Sciences Centre; Children's Hospital of Eastern Ontario; BC Children's Hospital; Izaak Walton Killam Health Centre; Stollery Children's Hospital; Alberta Children's Hospital; Montreal Children's Hospital; Western University; Child and Family Research Institute; Hospital for Sick Children; University of British Columbia","funders":"National Heart, Lung, and Blood Institute","keywords":"Biology; Cardiotoxicity; Anthracycline; Cancer research; Childhood cancer; Genetics; Cancer; Coding (social sciences); Oncology; Internal medicine; Chemotherapy; Breast cancer; Medicine","score_opus":0.0304694679611255,"score_gpt":0.33517033972507604,"score_spread":0.30470087176395055,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2227148039","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9982589,0.00013872117,0.00036637692,0.00016265453,0.000017189435,0.000009508338,0.00024757424,0.000017456467,0.00078169646],"genre_scores_gemma":[0.9991333,0.00006764897,0.00027679553,0.000041319163,0.000009720751,0.0000028555553,0.000116933545,0.000011761773,0.0003395143],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.999734,0.000067396555,0.000030378818,0.00006012225,0.000043742413,0.000064379274],"domain_scores_gemma":[0.9992725,0.00029225735,0.00023731301,0.000040743176,0.000034005207,0.0001231839],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00017590435,0.0005146254,0.00022761646,0.00059159246,0.00044910068,0.00027112412,0.00030069088,0.0006229242,0.0040671024],"category_scores_gemma":[0.0006979769,0.00015412892,0.00045578863,0.0005180091,0.0004955485,0.00011917349,0.00026925444,0.0005444397,0.00026860548],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0028195356,0.00037288465,0.2766289,0.00013251521,0.00034955103,0.03151711,0.0010547065,0.00149126,0.6704149,0.002276092,0.0009599975,0.011982565],"study_design_scores_gemma":[0.00022237952,0.0012767533,0.8891175,0.000112467555,0.0004309406,0.053048857,0.00080320874,0.0024272879,0.04712691,0.00079745695,0.0045716255,0.00006466011],"about_ca_topic_score_codex":0.005127036,"about_ca_topic_score_gemma":0.0051617897,"teacher_disagreement_score":0.005127036,"about_ca_system_score_codex":0.0004140119,"about_ca_system_score_gemma":0.0003394566,"threshold_uncertainty_score":0.013605773},"labels":[],"label_agreement":null},{"id":"W2229599978","doi":"10.1038/ng.3446","title":"The contribution of rare variation to prostate cancer heritability","year":2015,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Genetic and phenotypic traits in livestock","field":"Biochemistry, Genetics and Molecular Biology","cited_by":158,"is_retracted":false,"has_abstract":false,"route_ca_aff":false,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"","funders":"National Cancer Institute; Canadian Institutes of Health Research; Cancer Research UK","keywords":"Minor allele frequency; Prostate cancer; Biology; Single-nucleotide polymorphism; Heritability; Allele; Allele frequency; Genetic variation; Genetics; Cancer; Oncology; Genotype; Medicine; Gene","score_opus":0.0074508607399357205,"score_gpt":0.26408409465940774,"score_spread":0.256633233919472,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2229599978","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.98456603,0.0014738856,0.0110387355,0.00039583066,0.00007050312,0.000009460529,0.00047383332,0.00011965646,0.0018520857],"genre_scores_gemma":[0.9975948,0.00021835211,0.0013879841,0.0000620344,0.000047633595,0.0000073249753,0.00012593002,0.000036092595,0.0005198368],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99734265,0.0010351596,0.00015961306,0.00080649374,0.0004569229,0.00019925088],"domain_scores_gemma":[0.99336123,0.004579374,0.00071583403,0.0008365278,0.00022555179,0.00028139525],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0018353121,0.00044917886,0.00071690604,0.0014134645,0.0005465536,0.000716458,0.00065493316,0.0008344166,0.0035533023],"category_scores_gemma":[0.0047874297,0.00048417668,0.000576974,0.00082493597,0.0009394528,0.00041509213,0.0008468069,0.0010798203,0.0002409379],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0016493673,0.00018654593,0.59447265,0.00039279964,0.0030402748,0.008687022,0.0014063717,0.004664696,0.30913317,0.014041887,0.0008984219,0.061426863],"study_design_scores_gemma":[0.00006904754,0.0002032316,0.9691964,0.00007061813,0.0007283072,0.0076631797,0.00027181077,0.0050803972,0.00786953,0.0064251223,0.0023554142,0.00006681382],"about_ca_topic_score_codex":0.0019686832,"about_ca_topic_score_gemma":0.0022464017,"teacher_disagreement_score":0.0035533023,"about_ca_system_score_codex":0.0002482625,"about_ca_system_score_gemma":0.0002588671,"threshold_uncertainty_score":0.011886954},"labels":[],"label_agreement":null},{"id":"W2238851414","doi":"10.1038/ng.3396","title":"A comprehensive 1000 Genomes–based genome-wide association meta-analysis of coronary artery disease","year":2015,"lang":"en","type":"review","venue":"Nature Genetics","topic":"Genetic Associations and Epidemiology","field":"Biochemistry, Genetics and Molecular Biology","cited_by":2696,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Population Health Research Institute; Canadian Heart Research Centre; University of Ottawa","funders":"National Institute of Diabetes and Digestive and Kidney Diseases; National Heart, Lung, and Blood Institute; Medical Research Council; University of Oklahoma Health Sciences Center; National Institutes of Health; Nestec; Hjartavernd; Sydäntutkimussäätiö; Vetenskapsrådet; National Cancer Institute; Knut och Alice Wallenbergs Stiftelse; Erasmus Medisch Centrum; Erasmus Universiteit Rotterdam; National Institute for Health and Care Research; University of Oklahoma; School of Medicine, Boston University; European Commission; ZonMw; Amgen; Foundation for Cardiovascular Research; Uppsala Multidisciplinary Center for Advanced Computational Science; British Heart Foundation; Donald W. Reynolds Foundation; Nederlandse Organisatie voor Wetenschappelijk Onderzoek; Wellcome Trust; NHLBI Division of Intramural Research; Hjärt-Lungfonden","keywords":"Genome-wide association study; Biology; Single-nucleotide polymorphism; Genetic association; Genetics; Imputation (statistics); Coronary artery disease; Minor allele frequency; Genome; Genetic architecture; Haplotype; Meta-analysis; Allele frequency; 1000 Genomes Project; Allele; Gene; Quantitative trait locus; Genotype; Internal medicine; Medicine","score_opus":0.053539734851071025,"score_gpt":0.3356734980642567,"score_spread":0.28213376321318573,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2238851414","genre_codex":"review","genre_gemma":"review","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"review","genre_consensus":"review","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.0011726476,0.9940362,0.001884833,0.00135219,0.00032529558,0.000020493051,0.0007336139,0.000045062425,0.00042973674],"genre_scores_gemma":[0.013316652,0.97762764,0.004767701,0.0016157527,0.00079675857,0.000051784864,0.0014028469,0.00002787184,0.00039311877],"study_design_codex":"design_other","study_design_gemma":"meta_analysis","domain_scores_codex":[0.9984376,0.0005021016,0.00026699345,0.00035855194,0.00035787077,0.00007684763],"domain_scores_gemma":[0.9968363,0.0020505458,0.00033119702,0.00016584387,0.0004889195,0.00012727107],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0054455367,0.0013867248,0.003617106,0.002707205,0.00023848987,0.0011879224,0.0017668557,0.0012570681,0.0017202899],"category_scores_gemma":[0.007685276,0.0005791735,0.003002708,0.003923015,0.00035109132,0.00086588453,0.0012763409,0.0015236768,0.0004965291],"study_design_candidate":"meta_analysis","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00076571293,0.00006310641,0.01620264,0.030339848,0.026045078,0.00041204403,0.00009053051,0.0010744568,0.0013681522,0.0020138575,0.038344223,0.88328034],"study_design_scores_gemma":[0.0009088016,0.0006289157,0.15172282,0.029740337,0.14717835,0.0052311094,0.0002879641,0.0020035906,0.002109052,0.023513168,0.63627064,0.00040531036],"about_ca_topic_score_codex":0.004334123,"about_ca_topic_score_gemma":0.010920637,"teacher_disagreement_score":0.0054455367,"about_ca_system_score_codex":0.0006682816,"about_ca_system_score_gemma":0.0029065942,"threshold_uncertainty_score":0.028799117},"labels":[],"label_agreement":null},{"id":"W2264170040","doi":"10.1038/ng.3500","title":"MYB-QKI rearrangements in angiocentric glioma drive tumorigenicity through a tripartite mechanism","year":2016,"lang":"en","type":"review","venue":"Nature Genetics","topic":"Glioma Diagnosis and Treatment","field":"Medicine","cited_by":281,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"McGill University; McGill University Health Centre; Montreal Children's Hospital; Hospital for Sick Children","funders":"National Institute of General Medical Sciences; National Institute of Neurological Disorders and Stroke; National Human Genome Research Institute; National Cancer Institute; National Heart, Lung, and Blood Institute","keywords":"Biology; MYB; Carcinogenesis; Enhancer; Cancer research; Chromosomal translocation; Epigenetics; Glioma; Genetics; Transcription factor; Gene","score_opus":0.029976169475523833,"score_gpt":0.34406236242649946,"score_spread":0.3140861929509756,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2264170040","genre_codex":"review","genre_gemma":"review","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"review","genre_consensus":"review","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.0014853193,0.99431616,0.00096555526,0.00081987825,0.0002588198,0.000007806362,0.000047657504,0.000026793597,0.0020719501],"genre_scores_gemma":[0.01233308,0.98348016,0.0009903162,0.0005283192,0.00026523412,0.000015322057,0.000114915994,0.0000041347294,0.0022683726],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.999951,0.0000060540365,0.000006790216,0.0000115547455,0.000017594586,0.0000069985363],"domain_scores_gemma":[0.99994516,0.000019200608,0.000016379463,0.0000018240062,0.000011095442,0.000006443185],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00017667134,0.00036146078,0.00048692027,0.00045434106,0.00006760598,0.00033014454,0.00028369288,0.00039476505,0.0013530188],"category_scores_gemma":[0.00018671756,0.0001179877,0.00014723382,0.00035297594,0.00021894758,0.00041559816,0.00033978623,0.0007698412,0.00070531317],"study_design_candidate":"not_applicable","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00013415201,0.000024723595,0.0006228171,0.0061032907,0.000095619536,0.00048379682,0.00004155986,0.00034638817,0.020466492,0.0043385597,0.018209996,0.94913274],"study_design_scores_gemma":[0.000059424223,0.00012751725,0.0026846484,0.0013706639,0.0002245778,0.0041746474,0.000057381236,0.00028160008,0.0062857363,0.0033961826,0.98131096,0.000026661755],"about_ca_topic_score_codex":0.00027023815,"about_ca_topic_score_gemma":0.00072688644,"teacher_disagreement_score":0.0013530188,"about_ca_system_score_codex":0.00031552202,"about_ca_system_score_gemma":0.00043578033,"threshold_uncertainty_score":0.004526317},"labels":[],"label_agreement":null},{"id":"W2266573952","doi":"10.1038/ng.3383","title":"Genetic association analyses highlight biological pathways underlying mitral valve prolapse","year":2015,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Cardiac Valve Diseases and Treatments","field":"Medicine","cited_by":135,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Université Laval; Genome Canada; Institut universitaire de cardiologie et de pneumologie de Québec","funders":"National Center for Research Resources; National Heart, Lung, and Blood Institute; Fonds de Recherche du Québec - Santé; American Heart Association; Canadian Institutes of Health Research; Agence Nationale de la Recherche; Fondation Leducq; European Commission; National Institutes of Health; Sociedad Española de Cardiología; Massachusetts General Hospital; National Institute of General Medical Sciences","keywords":"Biology; Mitral valve prolapse; Zebrafish; Tensin; Genome-wide association study; Candidate gene; Genetics; Genetic association; Phenotype; Internal medicine; Mitral valve; Gene; Bioinformatics; Single-nucleotide polymorphism; Medicine; PTEN; Signal transduction; Genotype; PI3K/AKT/mTOR pathway","score_opus":0.09273949089582924,"score_gpt":0.3972723467989947,"score_spread":0.3045328559031655,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2266573952","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9712612,0.006278023,0.010004431,0.005518821,0.0003483948,0.000025738333,0.001638692,0.00014253703,0.0047820774],"genre_scores_gemma":[0.9921421,0.0019255314,0.0038441462,0.0005342553,0.00025999808,0.000011631932,0.0004015472,0.00004574954,0.0008350005],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9986865,0.00044309103,0.00012374471,0.00040907005,0.0002178718,0.00011977231],"domain_scores_gemma":[0.9962245,0.0024363918,0.0007912356,0.00020635084,0.00014386814,0.00019761526],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0013188953,0.0010743615,0.00048335487,0.0020971668,0.000578798,0.0014282212,0.0007447753,0.0011623828,0.0040398617],"category_scores_gemma":[0.0047091655,0.00043994546,0.0015493163,0.0016367938,0.0008404976,0.0006362737,0.0008208354,0.0013751176,0.0002842918],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0033566314,0.00033239526,0.7671385,0.0004972828,0.006022214,0.013593028,0.00077099004,0.0034700572,0.12577957,0.013543419,0.00347034,0.06202553],"study_design_scores_gemma":[0.00031222551,0.00035172552,0.93229294,0.00022872552,0.004097049,0.010330934,0.00058077485,0.0063576875,0.012358266,0.025080752,0.007899675,0.000109223736],"about_ca_topic_score_codex":0.0018046603,"about_ca_topic_score_gemma":0.002308366,"teacher_disagreement_score":0.0040398617,"about_ca_system_score_codex":0.0002714482,"about_ca_system_score_gemma":0.0004890402,"threshold_uncertainty_score":0.013514638},"labels":[],"label_agreement":null},{"id":"W2268489608","doi":"10.1038/ng.3495","title":"The genomic basis of parasitism in the Strongyloides clade of nematodes","year":2016,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Parasites and Host Interactions","field":"Immunology and Microbiology","cited_by":280,"is_retracted":false,"has_abstract":true,"route_ca_aff":false,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"","funders":"University of Pennsylvania; National Center for Research Resources; National Institute of Allergy and Infectious Diseases; University of Miyazaki; Japan Society for the Promotion of Science; Institute of Genetics; National Institutes of Health; Max-Planck-Gesellschaft; Wellcome Trust; Academia Sinica; Oregon State University; University of Bristol","keywords":"Biology; Strongyloides stercoralis; Strongyloides; Parasitism; Clade; Nematode; Strongyloidiasis; Genome; Evolutionary biology; Genetics; Gene; Zoology; Ecology; Host (biology); Helminths; Phylogenetics","score_opus":0.008714609401515158,"score_gpt":0.2863466382417927,"score_spread":0.27763202884027754,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2268489608","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.997783,0.00066727004,0.00036585194,0.00007909523,0.000006085469,0.0000057087827,0.0004978287,0.000013403216,0.000581786],"genre_scores_gemma":[0.9970968,0.0004902095,0.0006202883,0.00006332899,0.0000093960525,0.000008366018,0.0011365388,0.000008329238,0.0005669013],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99990904,0.000007779752,0.000005632085,0.00003654493,0.000021751166,0.000019359952],"domain_scores_gemma":[0.999824,0.000023749844,0.00007841049,0.000010821188,0.000018156747,0.00004497997],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00007313953,0.00018167567,0.00014322695,0.00038884894,0.00031031598,0.00028103744,0.00013715832,0.0002582732,0.0007394024],"category_scores_gemma":[0.0001772589,0.00014821647,0.00019463508,0.00030403968,0.00019850532,0.00020196434,0.00039885647,0.0002731148,0.00021645242],"study_design_candidate":"bench_or_experimental","study_design_consensus":"bench_or_experimental","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00018706812,0.000012574156,0.03497471,0.00010772928,0.000025471352,0.0004081227,0.000270044,0.00009597874,0.9574911,0.00016008092,0.00018146815,0.0060857474],"study_design_scores_gemma":[0.000013381802,0.0001071136,0.97292197,0.000032392163,0.000060580158,0.0011407688,0.0004546202,0.0005902709,0.021256493,0.000249191,0.0031563262,0.000016853479],"about_ca_topic_score_codex":0.001010841,"about_ca_topic_score_gemma":0.0023141978,"teacher_disagreement_score":0.001010841,"about_ca_system_score_codex":0.00014396869,"about_ca_system_score_gemma":0.00015809291,"threshold_uncertainty_score":0.0024735332},"labels":[],"label_agreement":null},{"id":"W2291123596","doi":"10.1038/ng.3521","title":"Breast cancer risk variants at 6q25 display different phenotype associations and regulate ESR1, RMND1 and CCDC170","year":2016,"lang":"en","type":"review","venue":"Nature Genetics","topic":"BRCA gene mutations in cancer","field":"Biochemistry, Genetics and Molecular Biology","cited_by":171,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Université Laval; Centre hospitalier universitaire de Québec; Public Health Ontario; Dalhousie University; University Health Network; Royal Victoria Hospital; University of Toronto; Lunenfeld-Tanenbaum Research Institute; Mount Sinai Hospital; McGill University","funders":"National Cancer Institute; Medical Research Council; Canadian Institutes of Health Research; National Institute for Health and Care Research; Cancer Research UK; Francis Crick Institute; Breast Cancer Research Foundation; U.S. Department of Defense; World Health Organization; Ministero dell'Università e della Ricerca; Università degli Studi di Firenze; National Institutes of Health; Ovarian Cancer Research Fund; Génome Québec; McGill University","keywords":"Biology; Phenotype; Breast cancer; Genetics; Cancer; Computational biology; Bioinformatics; Gene","score_opus":0.009259834890482333,"score_gpt":0.30231128343249064,"score_spread":0.2930514485420083,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2291123596","genre_codex":"review","genre_gemma":"review","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"review","genre_consensus":"review","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.00031231373,0.99751735,0.00031396697,0.00046791497,0.0002324567,0.000004796619,0.00007837237,0.000014555781,0.0010584317],"genre_scores_gemma":[0.0021330859,0.9950159,0.0005403395,0.00047112218,0.00021350074,0.000008898731,0.00018072095,0.0000044296257,0.0014320761],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.9998449,0.000019257142,0.000021983895,0.0000383774,0.00005863552,0.000016894486],"domain_scores_gemma":[0.9998005,0.00009099571,0.00003131989,0.0000068338018,0.000051726292,0.000018609855],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.000564865,0.00063592783,0.001091841,0.0010588241,0.00014951201,0.00077447604,0.0008262966,0.00076914596,0.0024922667],"category_scores_gemma":[0.00081251835,0.00020603964,0.00040556316,0.0010254439,0.000318673,0.0005363592,0.00043533312,0.0011100185,0.00095185754],"study_design_candidate":"not_applicable","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00014082027,0.000025815305,0.00083281775,0.007318495,0.00018435268,0.00037717496,0.00003968395,0.00039690724,0.0026598002,0.003174321,0.037944533,0.9469054],"study_design_scores_gemma":[0.000032327727,0.000038218142,0.0016911362,0.0014966434,0.00025675178,0.0015779472,0.00003787765,0.00009529398,0.00096084946,0.0014971673,0.99229664,0.000019144085],"about_ca_topic_score_codex":0.0013362309,"about_ca_topic_score_gemma":0.0032649748,"teacher_disagreement_score":0.0024922667,"about_ca_system_score_codex":0.00061760016,"about_ca_system_score_gemma":0.0009212396,"threshold_uncertainty_score":0.008337498},"labels":[],"label_agreement":null},{"id":"W2296550515","doi":"10.1038/ng.3526","title":"The spotted gar genome illuminates vertebrate evolution and facilitates human-teleost comparisons","year":2016,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Cancer-related molecular mechanisms research","field":"Biochemistry, Genetics and Molecular Biology","cited_by":671,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Victoria","funders":"Eunice Kennedy Shriver National Institute of Child Health and Human Development; National Human Genome Research Institute; National Institute of General Medical Sciences; Biomedical Research Council; Conselho Nacional de Desenvolvimento Científico e Tecnológico; Japan Society for the Promotion of Science; Directorate for Biological Sciences; Volkswagen Foundation; National Institutes of Health; National Center for Research Resources; National Institute of Allergy and Infectious Diseases; Agence Nationale de la Recherche; Ministry of National Education and Religious Affairs; Ministerio de Ciencia e Innovación; Generalitat de Catalunya; National Natural Science Foundation of China; Agency for Science, Technology and Research; Broad Institute; European Molecular Biology Laboratory; University of Oregon; Biotechnology and Biological Sciences Research Council; Wellcome Trust; Alexander von Humboldt-Stiftung; National Key Research and Development Program of China; Brinson Foundation; University of Chicago; Harvard University; Agència de Gestió d'Ajuts Universitaris i de Recerca; National Science Foundation","keywords":"Biology; Genome; Subfunctionalization; Vertebrate; Hox gene; Evolutionary biology; Lineage (genetic); Gene duplication; Gene; Genetics; Genome evolution; Human genome; Comparative genomics; Gene family; Genomics; Gene expression","score_opus":0.007567963335081685,"score_gpt":0.26428498693872027,"score_spread":0.25671702360363857,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2296550515","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.89465505,0.019373272,0.047110584,0.0071907216,0.0011371332,0.00008488503,0.009176276,0.002310307,0.018961748],"genre_scores_gemma":[0.9019631,0.008255368,0.075033866,0.0021555296,0.00058231666,0.00006831345,0.007084789,0.0005854131,0.004271291],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9997603,0.000046460715,0.000013331546,0.00006817395,0.00007600032,0.000035642242],"domain_scores_gemma":[0.9994972,0.00019400216,0.00007146864,0.00006646424,0.00008926555,0.000081560385],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0005889104,0.00031530551,0.00032359594,0.0012123482,0.00027432284,0.00071481266,0.00033124388,0.00057834416,0.0033515352],"category_scores_gemma":[0.00096084847,0.00021346114,0.00034896703,0.00071811874,0.00030887002,0.00034923927,0.00080160296,0.00070155336,0.0007516841],"study_design_candidate":"bench_or_experimental","study_design_consensus":"bench_or_experimental","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0018991065,0.00012168152,0.028892906,0.0008028997,0.00030808436,0.001918283,0.0008894836,0.0013901026,0.6343552,0.006536571,0.016496321,0.30638945],"study_design_scores_gemma":[0.0003112035,0.00045709588,0.24714461,0.0004404938,0.000590672,0.006634346,0.00090090954,0.006323966,0.19052258,0.016373372,0.5301807,0.00012002462],"about_ca_topic_score_codex":0.00074485544,"about_ca_topic_score_gemma":0.0029557098,"teacher_disagreement_score":0.0033515352,"about_ca_system_score_codex":0.0002010676,"about_ca_system_score_gemma":0.00025819096,"threshold_uncertainty_score":0.011211991},"labels":[],"label_agreement":null},{"id":"W2297994856","doi":"10.1038/ng.3528","title":"Analysis of five chronic inflammatory diseases identifies 27 new associations and highlights disease-specific patterns at shared loci","year":2016,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Genetic Associations and Epidemiology","field":"Biochemistry, Genetics and Molecular Biology","cited_by":785,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Toronto; Centre for Addiction and Mental Health","funders":"National Center for Research Resources; National Institute of Diabetes and Digestive and Kidney Diseases; National Institute of Arthritis and Musculoskeletal and Skin Diseases; National Institute of Allergy and Infectious Diseases; National Institutes of Health; Horizon 2020 Framework Programme; Novo Nordisk Fonden; Tartu Ülikool; National Institute of General Medical Sciences; National Institute for Health and Care Research; Bundesministerium für Bildung und Forschung; Novo Nordisk; Nederlandse Organisatie voor Wetenschappelijk Onderzoek; Vetenskapsrådet; Lundbeckfonden; Crohn's and Colitis UK; Exzellenzclusters Entzündungsforschung; Eesti Teadusagentuur; Deutsche Forschungsgemeinschaft; King's College London","keywords":"Biology; Genetics; Disease; Computational biology; Evolutionary biology; Internal medicine; Medicine","score_opus":0.00851114084369389,"score_gpt":0.2474958811752723,"score_spread":0.2389847403315784,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2297994856","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9966348,0.001020833,0.0010880753,0.00007193594,0.000007909102,0.000016590233,0.0005986864,0.000014999623,0.0005461435],"genre_scores_gemma":[0.9971674,0.0003433542,0.0014948247,0.00006179235,0.000011728548,0.00001765277,0.0006250959,0.000008929138,0.00026916122],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9983814,0.00041403182,0.00023072469,0.00042500652,0.0002690282,0.00027984087],"domain_scores_gemma":[0.9951474,0.002065844,0.0013949461,0.0004568266,0.00037171398,0.0005632642],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0017579442,0.0005486118,0.0007897109,0.0022373633,0.0009597999,0.001007884,0.0005695848,0.00050035707,0.0028009177],"category_scores_gemma":[0.0034650334,0.0002666291,0.0010454501,0.002817512,0.0008459907,0.00029850664,0.0012513609,0.00059736666,0.00029451426],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0011097367,0.000095475654,0.9704433,0.00014041737,0.00057613075,0.000874155,0.00033403139,0.00014843907,0.012735801,0.00024794016,0.0001668436,0.013127854],"study_design_scores_gemma":[0.00003134468,0.00016743176,0.99592495,0.000021644964,0.00036242948,0.000954361,0.00021393049,0.0001556269,0.0011817197,0.00026543005,0.0007076548,0.00001346427],"about_ca_topic_score_codex":0.0028859288,"about_ca_topic_score_gemma":0.004335683,"teacher_disagreement_score":0.0028859288,"about_ca_system_score_codex":0.00033527726,"about_ca_system_score_gemma":0.0007068568,"threshold_uncertainty_score":0.009369969},"labels":[],"label_agreement":null},{"id":"W2306878739","doi":"10.1038/ng.3536","title":"Genetic lineage tracing identifies endocardial origin of liver vasculature","year":2016,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Congenital heart defects research","field":"Biochemistry, Genetics and Molecular Biology","cited_by":109,"is_retracted":false,"has_abstract":false,"route_ca_aff":false,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"","funders":"Hospital for Sick Children","keywords":"Sinus venosus; Biology; Endocardium; Angiogenesis; Heart development; Organogenesis; Mesoderm; Embryonic stem cell; Anatomy; Pathology; Internal medicine; Cancer research; Genetics; Medicine","score_opus":0.010343370113821347,"score_gpt":0.2852573592086172,"score_spread":0.27491398909479586,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2306878739","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9267342,0.0014989271,0.06180024,0.0004552837,0.0000722598,0.000042714553,0.00050817826,0.00024102523,0.008647273],"genre_scores_gemma":[0.9669239,0.0010590043,0.02450162,0.000115744595,0.000021170199,0.000023651279,0.0004888991,0.00020302035,0.006663002],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99978775,0.000035870464,0.000015235833,0.000061395316,0.00005535882,0.000044402],"domain_scores_gemma":[0.99931836,0.0002595784,0.00014295023,0.00012033667,0.00007308588,0.000085678694],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00040335502,0.00023806344,0.0001965097,0.00080307206,0.00035245775,0.0011974524,0.00051471003,0.0006842976,0.0025957825],"category_scores_gemma":[0.00065125275,0.00041769267,0.00026132658,0.00022608295,0.00046585297,0.0005290527,0.0006698492,0.0015703256,0.0010406391],"study_design_candidate":"bench_or_experimental","study_design_consensus":"bench_or_experimental","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00006812795,0.000013956788,0.0020662944,0.000025624235,0.0000047664566,0.00019679927,0.00007882424,0.00025694034,0.9886409,0.0030883446,0.00009430185,0.0054653073],"study_design_scores_gemma":[0.0000228573,0.00005320496,0.010361127,0.00003132881,0.000031300347,0.001215803,0.00014465768,0.005704234,0.97436696,0.0009931397,0.007063697,0.000011628343],"about_ca_topic_score_codex":0.0010011623,"about_ca_topic_score_gemma":0.0020609833,"teacher_disagreement_score":0.0025957825,"about_ca_system_score_codex":0.00039357485,"about_ca_system_score_gemma":0.00027366582,"threshold_uncertainty_score":0.008683741},"labels":[],"label_agreement":null},{"id":"W2306906617","doi":"10.1038/ng.3562","title":"Five endometrial cancer risk loci identified through genome-wide association analysis","year":2016,"lang":"en","type":"review","venue":"Nature Genetics","topic":"Kruppel-like factors research","field":"Biochemistry, Genetics and Molecular Biology","cited_by":97,"is_retracted":false,"has_abstract":false,"route_ca_aff":false,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"","funders":"National Cancer Institute; Cancer Council Tasmania; Cancer Council Queensland; National Health and Medical Research Council; Medical Research Council; U.S. Public Health Service; QIMR Berghofer Medical Research Institute; Stockholms Läns Landsting; Helse Vest; Karolinska Institutet; Canadian Institutes of Health Research; Cancerfonden; Agency for Science, Technology and Research; Hunter Medical Research Institute; Vincent Fairfax Family Foundation; Norges Forskningsråd; Breast Cancer Research Foundation; University of Cambridge; Fred C. and Katherine B. Andersen Foundation; Academy of Medical Sciences; Wellcome Trust; Cancer Research UK; Universitetet i Bergen; National Institute for Health and Care Research; Haukeland Universitetssjukehus; Roswell Park Cancer Institute; Francis Crick Institute; Mayo Foundation for Medical Education and Research; National Institutes of Health; Ovarian Cancer Research Fund","keywords":"Genome-wide association study; Biology; Endometrial cancer; Locus (genetics); Genetics; Single-nucleotide polymorphism; Genetic association; Allele; Carcinogenesis; SNP; Chromatin; Gene; Cancer; Genotype","score_opus":0.0204624801207582,"score_gpt":0.3638280651513213,"score_spread":0.34336558503056314,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2306906617","genre_codex":"review","genre_gemma":"review","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"review","genre_consensus":"review","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.00076900754,0.9973014,0.000463768,0.00039367474,0.00011971061,0.0000051549905,0.000081122475,0.000015923086,0.0008503886],"genre_scores_gemma":[0.005041306,0.99245465,0.0009875492,0.0004562731,0.00014296784,0.000009692077,0.00019569266,0.0000035091632,0.00070834777],"study_design_codex":"design_other","study_design_gemma":"observational","domain_scores_codex":[0.99978536,0.000027104647,0.000034632078,0.000060522634,0.000065579516,0.000026729535],"domain_scores_gemma":[0.99962866,0.00017821732,0.00006975557,0.000014760742,0.0000714127,0.00003719974],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0008500321,0.00092205714,0.0014298122,0.0017998591,0.00021922246,0.0010523184,0.0010752416,0.0010773177,0.0020396078],"category_scores_gemma":[0.0008843139,0.00030848477,0.0005230712,0.0017591772,0.0005050359,0.00059188885,0.00075069984,0.0012810694,0.00094452366],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0003028122,0.00004520707,0.0027245982,0.009782486,0.00040896673,0.0009230611,0.000059921527,0.00034824587,0.004458129,0.0025009376,0.011223276,0.96722245],"study_design_scores_gemma":[0.0001556225,0.00020398859,0.015701413,0.0055367816,0.002093376,0.006619137,0.00021000896,0.00026758283,0.0054428354,0.0055033946,0.9581685,0.00009729547],"about_ca_topic_score_codex":0.0013004168,"about_ca_topic_score_gemma":0.002705138,"teacher_disagreement_score":0.0020396078,"about_ca_system_score_codex":0.00053060864,"about_ca_system_score_gemma":0.0011823215,"threshold_uncertainty_score":0.006823182},"labels":[],"label_agreement":null},{"id":"W2311083859","doi":"10.1038/ng.3531","title":"Genetic predisposition for beta cell fragility underlies type 1 and type 2 diabetes","year":2016,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Pancreatic function and diabetes","field":"Medicine","cited_by":149,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Université de Montréal; Hôpital Maisonneuve-Rosemont","funders":"National Institutes of Health; Biotechnology and Biological Sciences Research Council; Novo Nordisk Fonden; National Institute for Health and Care Research","keywords":"Beta cell; Biology; Genetic predisposition; Nod; Pancreatic islets; Type 1 diabetes; NOD mice; BETA (programming language); Type 2 diabetes; Diabetes mellitus; Immunology; Genetics; Fragility; Islet; Endocrinology; Gene","score_opus":0.00984346028777348,"score_gpt":0.24864144007972427,"score_spread":0.2387979797919508,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2311083859","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99285156,0.0015909409,0.0015785398,0.00084421824,0.00012504701,0.000015922036,0.0003059312,0.00008087868,0.0026068497],"genre_scores_gemma":[0.9973907,0.0007740789,0.00077781104,0.00013685756,0.00015446825,0.000008472233,0.00014239419,0.000029512963,0.00058578036],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9993799,0.0001941093,0.000055212364,0.00015141934,0.00013265046,0.000086759406],"domain_scores_gemma":[0.998801,0.00043243993,0.0004386621,0.00009556836,0.000059882084,0.00017240786],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00051232014,0.0013572294,0.0004856754,0.0021677508,0.0005954462,0.0009176115,0.00077247265,0.0016971139,0.0064578853],"category_scores_gemma":[0.0028111595,0.0004384475,0.00063481333,0.0013830207,0.0007538879,0.0005614889,0.00096543523,0.001191065,0.00033168282],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.003132794,0.0005141087,0.71725494,0.00028758758,0.0011169751,0.061650474,0.001032106,0.0010139334,0.17353824,0.0061393133,0.0023378306,0.031981684],"study_design_scores_gemma":[0.00018583832,0.00046447467,0.8681905,0.00022047032,0.0014018057,0.09848823,0.0008104662,0.0024869232,0.015680948,0.008168458,0.0038034907,0.000098315075],"about_ca_topic_score_codex":0.00082983274,"about_ca_topic_score_gemma":0.00052820996,"teacher_disagreement_score":0.0064578853,"about_ca_system_score_codex":0.00024949881,"about_ca_system_score_gemma":0.00022766355,"threshold_uncertainty_score":0.021603823},"labels":[],"label_agreement":null},{"id":"W2342647777","doi":"10.1038/ng.3555","title":"Concerted genomic targeting of H3K27 demethylase REF6 and chromatin-remodeling ATPase BRM in Arabidopsis","year":2016,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Plant Molecular Biology Research","field":"Agricultural and Biological Sciences","cited_by":239,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Agriculture and Agri-Food Canada; Western University","funders":"National Institute of General Medical Sciences; Howard Hughes Medical Institute","keywords":"Demethylase; Biology; Chromatin; Chromatin remodeling; Genetics; Bivalent chromatin; Gene; Zinc finger; Histone; ChIA-PET; Arabidopsis; Computational biology; Cell biology; Transcription factor; Mutant","score_opus":0.016257222504114283,"score_gpt":0.25334824374027054,"score_spread":0.23709102123615625,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2342647777","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9905391,0.0019546654,0.004114685,0.00020779928,0.00008377382,0.000019195111,0.00037935763,0.0003607546,0.0023407135],"genre_scores_gemma":[0.9945162,0.00024007446,0.0017209748,0.00010183488,0.000007561633,0.0000104938335,0.00034206695,0.00007788771,0.0029830288],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9998388,0.000012852827,0.0000096769845,0.00006718593,0.000036094083,0.00003531446],"domain_scores_gemma":[0.99984133,0.000022571372,0.00004550168,0.000038076643,0.00001434621,0.000038178092],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00019130777,0.00026732348,0.0003308437,0.0002090112,0.00020695674,0.00033028997,0.00040900777,0.000389374,0.0012269047],"category_scores_gemma":[0.00014421709,0.0003136933,0.00033028304,0.000107100896,0.00026512487,0.00027444342,0.00042413536,0.00072297273,0.00063671684],"study_design_candidate":"bench_or_experimental","study_design_consensus":"bench_or_experimental","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.000055599365,0.000006878749,0.00013884626,0.000015935382,0.000003066083,0.000027879001,0.0000053957638,0.000043850454,0.99866176,0.00013847771,0.000036207777,0.0008660563],"study_design_scores_gemma":[0.00002393739,0.00009420821,0.008990487,0.0000030155625,0.000019457062,0.00015959014,0.000046986355,0.0015960338,0.98583543,0.00014226114,0.003078286,0.000010098755],"about_ca_topic_score_codex":0.0012824105,"about_ca_topic_score_gemma":0.002918639,"teacher_disagreement_score":0.0012824105,"about_ca_system_score_codex":0.0007297425,"about_ca_system_score_gemma":0.00020607006,"threshold_uncertainty_score":0.0052946806},"labels":[],"label_agreement":null},{"id":"W2360159874","doi":"10.1038/ng.3572","title":"A method to decipher pleiotropy by detecting underlying heterogeneity driven by hidden subgroups applied to autoimmune and neuropsychiatric diseases","year":2016,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Genetic Associations and Epidemiology","field":"Biochemistry, Genetics and Molecular Biology","cited_by":70,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Toronto; Centre for Addiction and Mental Health","funders":"National Institute of Diabetes and Digestive and Kidney Diseases; National Human Genome Research Institute; National Institute of General Medical Sciences; National Institute of Arthritis and Musculoskeletal and Skin Diseases; National Institute of Allergy and Infectious Diseases; Medical Research Council; National Institutes of Health; Juvenile Diabetes Research Foundation International; Asan Institute for Life Sciences, Asan Medical Center; National Health and Medical Research Council; Fulbright Canada; National Institute of Child Health and Human Development; Fondation Brain Canada","keywords":"Pleiotropy; Biology; Genetic heterogeneity; Schizophrenia (object-oriented programming); Rheumatoid arthritis; Genotype; Allele; Genetics; Major depressive disorder; Immunology; Medicine; Psychiatry; Phenotype; Gene; Endocrinology","score_opus":0.010310513773653903,"score_gpt":0.29453199413231196,"score_spread":0.2842214803586581,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2360159874","genre_codex":"methods","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":null,"domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.0869297,0.00047216783,0.9081848,0.0004720336,0.00017270184,0.00013447725,0.001495921,0.0011771768,0.00096097525],"genre_scores_gemma":[0.46997386,0.0003050205,0.52459824,0.0003669783,0.0003334665,0.00045892678,0.0014287718,0.00029577885,0.0022389407],"study_design_codex":"design_other","study_design_gemma":"simulation_or_modeling","domain_scores_codex":[0.9970567,0.0014007109,0.00017200422,0.00091655744,0.00032795957,0.00012611935],"domain_scores_gemma":[0.9812859,0.013680087,0.00094070425,0.0028555735,0.0006637657,0.0005739504],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.007496849,0.0009452867,0.0013923866,0.0038859567,0.0009996336,0.0021188497,0.0013134923,0.0013632547,0.0033380678],"category_scores_gemma":[0.020724459,0.00065808,0.0021741467,0.0027315267,0.0010198113,0.0011324282,0.0015660855,0.0021436124,0.00060393295],"study_design_candidate":"simulation_or_modeling","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.002664295,0.0006384406,0.2920304,0.00064734655,0.0068478226,0.0016606718,0.0010451355,0.024829106,0.0924062,0.038142145,0.008121137,0.53096724],"study_design_scores_gemma":[0.001053272,0.00093512505,0.16387364,0.00013816013,0.0025289392,0.003093329,0.00044746307,0.54681647,0.01890089,0.24432603,0.017517468,0.0003692683],"about_ca_topic_score_codex":0.0018289019,"about_ca_topic_score_gemma":0.0019280454,"teacher_disagreement_score":0.007496849,"about_ca_system_score_codex":0.0002876842,"about_ca_system_score_gemma":0.0010059188,"threshold_uncertainty_score":0.03964758},"labels":[],"label_agreement":null},{"id":"W2366975997","doi":"10.1038/ng1001-133","title":"An SSLP marker–anchored BAC framework map of the mouse genome","year":2001,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Genomics and Chromatin Dynamics","field":"Biochemistry, Genetics and Molecular Biology","cited_by":17,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"BC Cancer Agency","funders":"Howard Hughes Medical Institute","keywords":"Biology; Genome; Computational biology; Genetics; Fingerprint (computing); Gene mapping; Gene; Computer science; Chromosome; Artificial intelligence","score_opus":0.0031199478145494154,"score_gpt":0.22425143276813797,"score_spread":0.22113148495358856,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2366975997","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.8933669,0.0054374454,0.073837414,0.00088038616,0.0001634301,0.00016896821,0.005494957,0.0011482651,0.01950227],"genre_scores_gemma":[0.92051804,0.0027413035,0.0400854,0.0003114829,0.000088307956,0.00013358516,0.011020093,0.00019187966,0.024909902],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.999928,0.0000049594873,0.000004169784,0.000024787554,0.000022319447,0.000015822061],"domain_scores_gemma":[0.99987936,0.000020754134,0.000020807964,0.0000127746725,0.000020166479,0.000046120917],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00012741306,0.00037802962,0.0001795968,0.0015665687,0.00046672835,0.0003104829,0.00043656636,0.00039015617,0.0032220401],"category_scores_gemma":[0.00014255442,0.00039637848,0.00039980037,0.00070598425,0.00031669435,0.00024560446,0.00034829119,0.0007328067,0.0015671677],"study_design_candidate":"bench_or_experimental","study_design_consensus":"bench_or_experimental","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00012849219,0.000022332364,0.00024552122,0.000052880496,0.000006789054,0.00014872542,0.0000436194,0.00013539717,0.9904095,0.0015892716,0.00020476109,0.0070127007],"study_design_scores_gemma":[0.00015874884,0.00053797336,0.056190517,0.000116055555,0.00017839593,0.0016743786,0.00017480052,0.0022841059,0.86991686,0.006993408,0.06173631,0.000038491078],"about_ca_topic_score_codex":0.0028750408,"about_ca_topic_score_gemma":0.004572182,"teacher_disagreement_score":0.0032220401,"about_ca_system_score_codex":0.0003533276,"about_ca_system_score_gemma":0.00041148686,"threshold_uncertainty_score":0.010778844},"labels":[],"label_agreement":null},{"id":"W2398435542","doi":"10.1038/ng.3578","title":"NANS-mediated synthesis of sialic acid is required for brain and skeletal development","year":2016,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Glycosylation and Glycoproteins Research","field":"Biochemistry, Genetics and Molecular Biology","cited_by":166,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Toronto; St. Michael's Hospital; Child and Family Research Institute; University of British Columbia","funders":"Canadian Institutes of Health Research; Université de Lausanne; University of British Columbia","keywords":"Sialic acid; Biology; Biochemistry; Phenotype; Gene knockdown; Metabolism; Cell biology; Gene","score_opus":0.010459431313497806,"score_gpt":0.27957889604183167,"score_spread":0.26911946472833387,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2398435542","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.97282267,0.002557807,0.015014047,0.00036333178,0.00010798603,0.000042907694,0.00092577306,0.00028427233,0.007881309],"genre_scores_gemma":[0.9788811,0.0012851162,0.0067895884,0.00010143729,0.000018912335,0.00003278665,0.0014844958,0.0001296537,0.011276806],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99986565,0.000015015348,0.000012499706,0.000035278717,0.00004048847,0.000031005893],"domain_scores_gemma":[0.9997348,0.000036927337,0.00007976077,0.00003678758,0.00003954704,0.000072217175],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00018252473,0.0004973723,0.00023174033,0.00033563463,0.00025343386,0.000619815,0.00029314918,0.00037090195,0.0014406143],"category_scores_gemma":[0.00018193206,0.00038052193,0.00031530342,0.00014967562,0.00047536648,0.0002981616,0.0005729388,0.00071289594,0.00073943136],"study_design_candidate":"bench_or_experimental","study_design_consensus":"bench_or_experimental","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00007865963,0.0000039314064,0.00028889626,0.000016394097,0.000004008985,0.000112279224,0.00000888181,0.00006471939,0.9978555,0.00057831896,0.000036109126,0.00095231005],"study_design_scores_gemma":[0.000008421544,0.000035863988,0.010733898,0.00000857982,0.000014421691,0.00034369473,0.00004388331,0.0008391046,0.9836875,0.0003977924,0.0038803408,0.000006487274],"about_ca_topic_score_codex":0.002296985,"about_ca_topic_score_gemma":0.0061794375,"teacher_disagreement_score":0.002296985,"about_ca_system_score_codex":0.0007443048,"about_ca_system_score_gemma":0.0006712068,"threshold_uncertainty_score":0.0054003},"labels":[],"label_agreement":null},{"id":"W2402730620","doi":"10.1038/ng.3573","title":"Divergent modes of clonal spread and intraperitoneal mixing in high-grade serous ovarian cancer","year":2016,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Cancer Genomics and Diagnostics","field":"Biochemistry, Genetics and Molecular Biology","cited_by":367,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Vancouver General Hospital; Canada's Michael Smith Genome Sciences Centre; Child and Family Research Institute; BC Cancer Agency; Simon Fraser University; University of British Columbia","funders":"Canadian Institutes of Health Research","keywords":"Biology; Serous fluid; Ovarian cancer; Phylogenetic tree; Somatic evolution in cancer; Ovary; Genetics; Genome; Cancer; Gene","score_opus":0.006230294401528789,"score_gpt":0.24467982943975294,"score_spread":0.23844953503822416,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2402730620","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99679875,0.00041274956,0.0015960562,0.000027126935,0.0000027367778,0.0000104465125,0.000021750942,0.000025813237,0.0011045376],"genre_scores_gemma":[0.999015,0.00011948879,0.00051384704,0.000010741291,0.0000029924302,0.0000070499286,0.000031804793,0.000007609622,0.00029144427],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99979,0.00006187138,0.000015425258,0.00002623169,0.000056136796,0.00005035368],"domain_scores_gemma":[0.9995197,0.00018528766,0.00009050079,0.000085612795,0.000053882355,0.00006497996],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00038888326,0.00012343777,0.0001835891,0.00093181833,0.00018639346,0.0008563212,0.00022631802,0.00028970808,0.0009722775],"category_scores_gemma":[0.0013154873,0.00018563311,0.00013983728,0.00034557478,0.00030540454,0.0003656658,0.0005673373,0.00037460646,0.00023556734],"study_design_candidate":"bench_or_experimental","study_design_consensus":"bench_or_experimental","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0016532713,0.00014604398,0.24852571,0.00010239313,0.000059730224,0.0016858766,0.0014161543,0.0027924043,0.66944855,0.007686644,0.00038480587,0.06609847],"study_design_scores_gemma":[0.000191343,0.0009948144,0.67654,0.000060835508,0.00016545324,0.014393058,0.0026045777,0.030922288,0.25912917,0.0071278503,0.007796861,0.00007372415],"about_ca_topic_score_codex":0.00035284995,"about_ca_topic_score_gemma":0.00047683824,"teacher_disagreement_score":0.0009722775,"about_ca_system_score_codex":0.00022542085,"about_ca_system_score_gemma":0.0001120583,"threshold_uncertainty_score":0.0032525659},"labels":[],"label_agreement":null},{"id":"W2416742466","doi":"10.1038/ng.3589","title":"Identification of TMEM230 mutations in familial Parkinson's disease","year":2016,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Cellular transport and secretion","field":"Biochemistry, Genetics and Molecular Biology","cited_by":176,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Saskatchewan; Saskatchewan Health Authority","funders":"National Institute of Neurological Disorders and Stroke; National Cancer Institute; National Institute on Aging","keywords":"Biology; Identification (biology); Genetics; Parkinson's disease; Disease; Mutation; Computational biology; Gene; Internal medicine","score_opus":0.0051126353269230485,"score_gpt":0.2340678353364784,"score_spread":0.22895520000955535,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2416742466","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9974074,0.00077044737,0.0004260999,0.000095394615,0.000045102453,0.000012228503,0.00022960927,0.000031054355,0.0009827594],"genre_scores_gemma":[0.99861014,0.00018625981,0.0005257113,0.000053580756,0.000026763093,0.0000073647307,0.00016848305,0.000013865905,0.00040778852],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.999688,0.00004059184,0.00007164616,0.0000760286,0.0000855757,0.00003817584],"domain_scores_gemma":[0.9995921,0.0001205899,0.00012414547,0.000018624813,0.000049684924,0.000094758405],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00028365693,0.0010669352,0.00051953853,0.0019216659,0.000550482,0.000657701,0.00046937182,0.001649107,0.0018360295],"category_scores_gemma":[0.0011269045,0.00038171833,0.00044531666,0.00083257793,0.00050657947,0.00025506114,0.0004873807,0.00040334254,0.0005800002],"study_design_candidate":"bench_or_experimental","study_design_consensus":"bench_or_experimental","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0019695258,0.00021429216,0.098686464,0.00021988293,0.00027859685,0.15985477,0.00079016207,0.0010147692,0.71391267,0.00087336364,0.0011559727,0.021029487],"study_design_scores_gemma":[0.00024406821,0.0011228337,0.44326642,0.00013916471,0.00059485505,0.34955692,0.00061473774,0.0044978326,0.19062886,0.0013569371,0.007857875,0.000119417746],"about_ca_topic_score_codex":0.0010917551,"about_ca_topic_score_gemma":0.0010484678,"teacher_disagreement_score":0.0019216659,"about_ca_system_score_codex":0.00041701674,"about_ca_system_score_gemma":0.00017607331,"threshold_uncertainty_score":0.0061421394},"labels":[],"label_agreement":null},{"id":"W2437351093","doi":"10.1038/ng.3668","title":"Discovery and refinement of genetic loci associated with cardiometabolic risk using dense imputation maps","year":2016,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Genetic Associations and Epidemiology","field":"Biochemistry, Genetics and Molecular Biology","cited_by":97,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"McGill University; Jewish General Hospital","funders":"National Heart, Lung, and Blood Institute; National Institute on Aging; Medical Research Council; National Institutes of Health; European Commission; National Institute for Health and Care Research; British Heart Foundation; Wellcome Trust","keywords":"Imputation (statistics); Biology; Genome-wide association study; Quantitative trait locus; 1000 Genomes Project; Minor allele frequency; Genetic architecture; Genetic association; Genetics; Trait; Allele; Allele frequency; Computational biology; Genotype; Single-nucleotide polymorphism; Gene; Missing data; Statistics","score_opus":0.006885454692681649,"score_gpt":0.24846218727816535,"score_spread":0.2415767325854837,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2437351093","genre_codex":"methods","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":null,"domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.3305086,0.00088251365,0.6591993,0.0008214588,0.00012204284,0.00022232106,0.0041036373,0.0017960714,0.0023440616],"genre_scores_gemma":[0.7361265,0.0003776697,0.25461504,0.00029289335,0.00007905191,0.00022251636,0.006275046,0.00028569897,0.0017255751],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99321485,0.003606594,0.00038538926,0.0014336767,0.00075455767,0.00060492725],"domain_scores_gemma":[0.9684504,0.020440504,0.0012224362,0.007534753,0.0017239705,0.0006278565],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.01305726,0.0014170989,0.0026513278,0.0036388936,0.0019136391,0.0028609748,0.00441742,0.0017227902,0.004976231],"category_scores_gemma":[0.048978608,0.0018969409,0.004468781,0.0041974834,0.0010813789,0.001464974,0.0031354036,0.003982567,0.0013713517],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.002708344,0.0009439834,0.4916675,0.00073549617,0.008582662,0.0038259688,0.0025794425,0.16252422,0.022794599,0.038065683,0.009406548,0.25616553],"study_design_scores_gemma":[0.0014946596,0.00051310076,0.21140769,0.00028681906,0.004811112,0.0025247855,0.0006772314,0.66283584,0.008064545,0.09150228,0.015561281,0.00032059566],"about_ca_topic_score_codex":0.021033512,"about_ca_topic_score_gemma":0.020503905,"teacher_disagreement_score":0.021033512,"about_ca_system_score_codex":0.00072944316,"about_ca_system_score_gemma":0.00237535,"threshold_uncertainty_score":0.069054246},"labels":[],"label_agreement":null},{"id":"W2470439906","doi":"10.1038/ng.3499","title":"Analysis of five years of controlled access and data sharing compliance at the International Cancer Genome Consortium","year":2016,"lang":"en","type":"letter","venue":"Nature Genetics","topic":"Ethics in Clinical Research","field":"Medicine","cited_by":16,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Ontario Institute for Cancer Research; McGill University","funders":"","keywords":"Biology; Genome; Cancer; Compliance (psychology); Genetics; Computational biology; Gene","score_opus":0.38139663352041053,"score_gpt":0.5693888942973265,"score_spread":0.187992260776916,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2470439906","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":"reproducibility","model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":"reproducibility","domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9061851,0.0006528499,0.0037657234,0.07702329,0.00035253947,0.000513806,0.0041586254,0.00011155942,0.007236518],"genre_scores_gemma":[0.9798105,0.0001241612,0.0019991542,0.013714228,0.00013409236,0.00083384366,0.001456747,0.00006671385,0.0018605674],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.76122856,0.16029584,0.014651298,0.01030341,0.03876429,0.014756578],"domain_scores_gemma":[0.3216025,0.38637266,0.10550522,0.08594224,0.079162836,0.021414591],"candidate_categories":["metaresearch","open_science"],"consensus_categories":[],"category_scores_codex":[0.18205918,0.00023362138,0.0007061569,0.0019701049,0.006565556,0.006119216,0.003423781,0.005575918,0.002574387],"category_scores_gemma":[0.4096178,0.00063309347,0.0008483717,0.006421211,0.0048156125,0.0035042095,0.006514498,0.006425435,0.00045644815],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0026847045,0.0010853783,0.8270976,0.00023672536,0.000760795,0.0014638886,0.03555708,0.0009189604,0.0005530881,0.013651339,0.058268994,0.05772139],"study_design_scores_gemma":[0.00037465684,0.0012391486,0.9020314,0.00059859594,0.00041231,0.00090624206,0.02076352,0.0033037644,0.0017202095,0.0064480146,0.061871465,0.00033070883],"about_ca_topic_score_codex":0.07225588,"about_ca_topic_score_gemma":0.05269331,"teacher_disagreement_score":0.9965762,"about_ca_system_score_codex":0.013740409,"about_ca_system_score_gemma":0.03563632,"threshold_uncertainty_score":0.9628325},"labels":[{"model":"gemma","categories":["metaresearch","open_science"],"domain":"reproducibility","study_design":"observational","genre":"empirical","about_ca_system":false,"about_ca_topic":false,"confidence":"low"},{"model":"gpt","categories":["metaresearch","open_science"],"domain":"reproducibility","study_design":"observational","genre":"empirical","about_ca_system":false,"about_ca_topic":false,"confidence":"medium"}],"label_agreement":"agree"},{"id":"W2474640767","doi":"10.1038/ng.3615","title":"Genomic analysis of snub-nosed monkeys (Rhinopithecus) identifies genes and processes related to high-altitude adaptation","year":2016,"lang":"en","type":"article","venue":"Nature Genetics","topic":"High Altitude and Hypoxia","field":"Biochemistry, Genetics and Molecular Biology","cited_by":153,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Toronto","funders":"National Program for Support of Top-notch Young Professionals; Chinese Academy of Sciences; State Key Laboratory of Genetic Resources and Evolution; National Natural Science Foundation of China","keywords":"Biology; Adaptation (eye); Effects of high altitude on humans; Gene; Evolutionary biology; Zoology; Genetics; Anatomy","score_opus":0.006276739414395052,"score_gpt":0.24399807342033417,"score_spread":0.23772133400593912,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2474640767","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99613416,0.0006425602,0.0012609155,0.00005482937,0.000010547668,0.000013240797,0.0011609416,0.00003170939,0.00069117115],"genre_scores_gemma":[0.98755044,0.00073696853,0.004662918,0.00013508977,0.000022194581,0.000030312047,0.005494454,0.000026477115,0.0013411279],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.99994516,0.0000050794174,0.0000031224433,0.000024342593,0.00001284123,0.000009408672],"domain_scores_gemma":[0.9998741,0.000025112136,0.000038958882,0.000013975088,0.00002250273,0.000025282072],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00008170899,0.00024684824,0.00019385165,0.00045311768,0.0002922478,0.0002682546,0.00013477785,0.00027022525,0.0008306203],"category_scores_gemma":[0.0002121943,0.00010894251,0.00035828975,0.00041249758,0.00016338773,0.00009529479,0.00024027925,0.0003491259,0.0003185597],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00026010338,0.00002279409,0.032244213,0.00012266406,0.00009405015,0.00054506934,0.0002291098,0.00019043023,0.9533302,0.00010754445,0.00015964085,0.012694132],"study_design_scores_gemma":[0.000019201296,0.00023558349,0.92627525,0.000022486429,0.00020003325,0.002051083,0.00035663354,0.0015807757,0.058106545,0.0002238453,0.0109066125,0.000021872092],"about_ca_topic_score_codex":0.0011291745,"about_ca_topic_score_gemma":0.002962568,"teacher_disagreement_score":0.0011291745,"about_ca_system_score_codex":0.00013295164,"about_ca_system_score_gemma":0.00012342399,"threshold_uncertainty_score":0.002778709},"labels":[],"label_agreement":null},{"id":"W2475605691","doi":"10.1038/ng.3611","title":"Genomic analysis of 6,000-year-old cultivated grain illuminates the domestication history of barley","year":2016,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Genetic diversity and population structure","field":"Biochemistry, Genetics and Molecular Biology","cited_by":167,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of British Columbia","funders":"National Institute of Food and Agriculture; University of Dundee; University of Minnesota; U.S. Department of Agriculture","keywords":"Domestication; Biology; Crop; Cave; Sympatric speciation; Lineage (genetic); Introgression; Extant taxon; Botany; Evolutionary biology; Zoology; Ecology; Gene; Genetics","score_opus":0.006750667490119393,"score_gpt":0.22479162359721494,"score_spread":0.21804095610709553,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2475605691","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99880743,0.00009989053,0.00028539056,0.000016438244,0.0000036082938,0.0000010499713,0.00052587484,0.000005891948,0.0002544271],"genre_scores_gemma":[0.9968863,0.00014474856,0.00048815104,0.000029057333,0.000007155955,0.000002881047,0.0016213914,0.000015711115,0.0008046746],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9999536,0.0000042907354,0.0000038133378,0.000017793816,0.000007516964,0.0000129508335],"domain_scores_gemma":[0.9998373,0.000052038784,0.00003301146,0.000016671023,0.000018928344,0.00004205705],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00010858573,0.00012015687,0.00018886678,0.0005707755,0.00027206354,0.00035549726,0.00014902707,0.00020529621,0.000656391],"category_scores_gemma":[0.00019421,0.00011781355,0.00027566176,0.0005727098,0.00021382066,0.00016288683,0.00024016564,0.0002789015,0.0002339176],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00054161117,0.000051052717,0.08643719,0.000033899643,0.000044979595,0.0004281789,0.0007216405,0.00017979299,0.90153867,0.00021404953,0.00012327025,0.009685541],"study_design_scores_gemma":[0.0000032786163,0.00004260123,0.98738676,0.0000025658796,0.000017864459,0.00023011414,0.00019128268,0.0001321583,0.010655855,0.00006088051,0.0012724572,0.0000042993847],"about_ca_topic_score_codex":0.00363096,"about_ca_topic_score_gemma":0.006871388,"teacher_disagreement_score":0.00363096,"about_ca_system_score_codex":0.00023634911,"about_ca_system_score_gemma":0.00011424128,"threshold_uncertainty_score":0.007219672},"labels":[],"label_agreement":null},{"id":"W2498993352","doi":"10.1038/ng.3626","title":"NEK1 variants confer susceptibility to amyotrophic lateral sclerosis","year":2016,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Amyotrophic Lateral Sclerosis Research","field":"Medicine","cited_by":294,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"McGill University; Montreal Neurological Institute and Hospital","funders":"National Institute of Neurological Disorders and Stroke; National Heart, Lung, and Blood Institute; Instituto de Salud Carlos III; National Health and Medical Research Council; Medical Research Council; National Institutes of Health; Deutsche Gesellschaft für Muskelkranke; National Human Genome Research Institute; Fondazione Italiana di Ricerca per la Sclerosi Laterale Amiotrofica; Fondation Charcot; University of Toronto; Ministero della Salute; ZonMw; Case Western Reserve University; Belgian Federal Science Policy Office; Deutsche Forschungsgemeinschaft; Bundesministerium für Bildung und Forschung; National Institute on Aging; National Institute for Health and Care Research; Vlaamse regering; Istituto Auxologico Italiano; National Alzheimer's Coordinating Center; Vanderbilt University; EU Joint Programme – Neurodegenerative Disease Research; University of Pennsylvania; Motor Neurone Disease Association; South London and Maudsley NHS Foundation Trust; Massachusetts Institute of Technology; Wellcome Trust; Canadian Institutes of Health Research; Fonds Wetenschappelijk Onderzoek; German Network for Motor Neuron Diseases; Muscular Dystrophy Association; King's College London; Fundación Española para el Fomento de la Investigación de la Esclerosis Lateral Amiotrófica; ALS Therapy Alliance; E-Rare; Howard Hughes Medical Institute; University of Miami; Broad Institute","keywords":"Amyotrophic lateral sclerosis; Biology; Loss function; Genetics; Candidate gene; Gene; Genetic association; Disease; Computational biology; Genotype; Single-nucleotide polymorphism; Phenotype; Pathology; Medicine","score_opus":0.033713816477818896,"score_gpt":0.30896234900055086,"score_spread":0.27524853252273196,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2498993352","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9953962,0.00051257724,0.0005486595,0.00032653406,0.00008758056,0.00000936745,0.0005948797,0.000031589585,0.002492623],"genre_scores_gemma":[0.9978084,0.000095573414,0.00034160187,0.000080991056,0.000038319395,0.0000056746762,0.0003080165,0.000023844026,0.0012976036],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99959666,0.00009450478,0.00007122202,0.000121573576,0.000058978498,0.00005698609],"domain_scores_gemma":[0.99898964,0.00039756138,0.00029826193,0.0000844637,0.000068984154,0.00016101122],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00035719495,0.0010047432,0.00051778817,0.00078304135,0.000800872,0.00070732343,0.00067718455,0.0016191824,0.01071802],"category_scores_gemma":[0.0017211353,0.00032708686,0.0007015293,0.00068294926,0.0004401082,0.00042715867,0.0006908038,0.0008829293,0.001098312],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.019481694,0.00077164086,0.45718455,0.0005418991,0.002872633,0.03855727,0.0024754705,0.0034971477,0.43450072,0.004619084,0.0046434114,0.030854471],"study_design_scores_gemma":[0.00088946184,0.0009335234,0.8909354,0.00034364488,0.0019350424,0.049912162,0.0010267779,0.0042093596,0.031616084,0.005832669,0.012149969,0.00021577408],"about_ca_topic_score_codex":0.0017828505,"about_ca_topic_score_gemma":0.0020191523,"teacher_disagreement_score":0.01071802,"about_ca_system_score_codex":0.00033876172,"about_ca_system_score_gemma":0.00018788752,"threshold_uncertainty_score":0.035855353},"labels":[],"label_agreement":null},{"id":"W2500269539","doi":"10.1038/ng.3627","title":"Distinct genetic architectures for syndromic and nonsyndromic congenital heart defects identified by exome sequencing","year":2016,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Congenital heart defects research","field":"Biochemistry, Genetics and Molecular Biology","cited_by":467,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Hospital for Sick Children","funders":"Medical Research Council; National Institute for Health and Care Research; Canadian Institutes of Health Research; European Commission; British Heart Foundation; Wellcome Trust","keywords":"Exome sequencing; Proband; Biology; Exome; Genetics; Sibling; Gene; Mutation","score_opus":0.009419971140601887,"score_gpt":0.2745167145876459,"score_spread":0.26509674344704404,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2500269539","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9934749,0.00038568504,0.0038451736,0.00016485347,0.0000242733,0.000024342684,0.0005737978,0.000067570094,0.0014393991],"genre_scores_gemma":[0.99405515,0.00038052167,0.0039785164,0.0001218383,0.000026052785,0.000024858127,0.00068634027,0.00006223842,0.00066440966],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.99958223,0.00005729102,0.000066323504,0.0001315202,0.000089619214,0.00007298662],"domain_scores_gemma":[0.9991561,0.00032246287,0.0002649686,0.000093708,0.000075982054,0.00008675503],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00037243846,0.00079667225,0.00040918423,0.0017870434,0.00029658558,0.00066299876,0.00047160953,0.0009743023,0.002876519],"category_scores_gemma":[0.0012305246,0.0003762277,0.000760506,0.0005546763,0.00082409097,0.00053654046,0.0009113238,0.0006881495,0.00041517345],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0018707707,0.00012214649,0.12650602,0.00019217457,0.00033505855,0.026472624,0.0005813461,0.0022288656,0.81361765,0.009031931,0.00065578974,0.018385556],"study_design_scores_gemma":[0.00031640285,0.0004717582,0.75518334,0.0002583538,0.0010714423,0.08331139,0.00075136824,0.011110981,0.13079087,0.011098929,0.0054970467,0.00013823515],"about_ca_topic_score_codex":0.0004906268,"about_ca_topic_score_gemma":0.0012453716,"teacher_disagreement_score":0.002876519,"about_ca_system_score_codex":0.00022542624,"about_ca_system_score_gemma":0.00031365472,"threshold_uncertainty_score":0.0096229315},"labels":[],"label_agreement":null},{"id":"W2508727752","doi":"10.1038/ng.3650","title":"Noncoding somatic and inherited single-nucleotide variants converge to promote ESR1 expression in breast cancer","year":2016,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Cancer Genomics and Diagnostics","field":"Biochemistry, Genetics and Molecular Biology","cited_by":105,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Princess Margaret Cancer Centre; Ontario Institute for Cancer Research; University of Toronto; University Health Network","funders":"National Cancer Institute; Canadian Institutes of Health Research","keywords":"Estrogen receptor alpha; Biology; Breast cancer; Enhancer; Estrogen receptor; Genetics; Single-nucleotide polymorphism; Cancer research; Somatic cell; Gene; Transcription factor; Cancer; Genotype","score_opus":0.006929196737173543,"score_gpt":0.24466751449420665,"score_spread":0.2377383177570331,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2508727752","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9942206,0.0011072429,0.002453985,0.0002331309,0.00006550747,0.000007692193,0.00021328879,0.00008500288,0.0016135767],"genre_scores_gemma":[0.99794585,0.00022149135,0.00080126524,0.00009425158,0.000023043307,0.000004734278,0.00009818454,0.0000349395,0.0007761139],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9996412,0.00006908796,0.000040794606,0.00006708891,0.0001368525,0.000045087825],"domain_scores_gemma":[0.9994754,0.00021615013,0.000102439844,0.000061190054,0.00004710582,0.00009772259],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00039707718,0.00021050057,0.00032040733,0.0003979304,0.00016977297,0.0004177357,0.00033342658,0.0004986913,0.0021659331],"category_scores_gemma":[0.00069221476,0.000224831,0.0003243131,0.00022876674,0.00032910687,0.00016826387,0.00042308503,0.0005735535,0.0006004142],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0003581678,0.000038841332,0.0068132924,0.000040256276,0.00004318184,0.0007697926,0.00004429403,0.00051863154,0.98533,0.0007830367,0.00017346526,0.0050870236],"study_design_scores_gemma":[0.00015552345,0.0005413196,0.25872883,0.000051463943,0.00023184686,0.008482119,0.00020687032,0.008356225,0.7137735,0.0026405964,0.006780614,0.00005109141],"about_ca_topic_score_codex":0.00023499956,"about_ca_topic_score_gemma":0.000498026,"teacher_disagreement_score":0.0021659331,"about_ca_system_score_codex":0.00018827415,"about_ca_system_score_gemma":0.00013487182,"threshold_uncertainty_score":0.007245779},"labels":[],"label_agreement":null},{"id":"W2511381148","doi":"10.1038/ng.3637","title":"Modulation of long noncoding RNAs by risk SNPs underlying genetic predispositions to prostate cancer","year":2016,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Cancer-related molecular mechanisms research","field":"Biochemistry, Genetics and Molecular Biology","cited_by":232,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Toronto; Ontario Institute for Cancer Research; Princess Margaret Cancer Centre; University Health Network","funders":"National Cancer Institute; National Heart, Lung, and Blood Institute; Canadian Institutes of Health Research","keywords":"Biology; Prostate cancer; Single-nucleotide polymorphism; Enhancer; Genome-wide association study; Androgen receptor; Long non-coding RNA; Transcriptome; Prostate; Genetics; Cancer research; Transcription factor; SNP; Cancer; Gene; Downregulation and upregulation; Gene expression; Genotype","score_opus":0.00940753791111977,"score_gpt":0.30477978069196937,"score_spread":0.2953722427808496,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2511381148","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9957716,0.00067226915,0.0021785123,0.00013562743,0.00003638879,0.000005641488,0.00030833486,0.00003649663,0.00085507624],"genre_scores_gemma":[0.9989513,0.00009155987,0.00046316814,0.000054476368,0.000019461007,0.0000035801152,0.000074770905,0.00001715099,0.00032462773],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9996124,0.00011452089,0.000028647017,0.00012727085,0.00006649891,0.000050778028],"domain_scores_gemma":[0.9991099,0.00032806318,0.00033893925,0.000075423304,0.00004627449,0.00010122191],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0002596467,0.00031968844,0.00022362842,0.00044805606,0.00019171662,0.0004297458,0.00023247971,0.00042532553,0.0025787866],"category_scores_gemma":[0.00099119,0.00027129994,0.00030949432,0.00030894598,0.0002571106,0.00018173164,0.00024374592,0.0004734922,0.00029657118],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0015873273,0.00009732492,0.12827559,0.00010034677,0.00047891305,0.0011866366,0.00030992483,0.00086293794,0.8565739,0.0013763098,0.0003534061,0.008797406],"study_design_scores_gemma":[0.00006483814,0.0003541307,0.92914283,0.000028921791,0.00037574873,0.001673541,0.00019525553,0.0035445136,0.061833095,0.0014685177,0.0012762651,0.00004230299],"about_ca_topic_score_codex":0.00074885925,"about_ca_topic_score_gemma":0.0009677892,"teacher_disagreement_score":0.0025787866,"about_ca_system_score_codex":0.00012413572,"about_ca_system_score_gemma":0.00012443935,"threshold_uncertainty_score":0.008626938},"labels":[],"label_agreement":null},{"id":"W2511515754","doi":"10.1038/ng.3643","title":"A reference panel of 64,976 haplotypes for genotype imputation","year":2016,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Genetic Associations and Epidemiology","field":"Biochemistry, Genetics and Molecular Biology","cited_by":3273,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"McGill University; University of Toronto; Centre for Addiction and Mental Health","funders":"National Institute of Diabetes and Digestive and Kidney Diseases; National Institute on Drug Abuse; National Eye Institute; National Institute on Aging; National Cancer Institute; British Heart Foundation; National Institute on Alcohol Abuse and Alcoholism; National Heart, Lung, and Blood Institute; National Institute of Mental Health; Versus Arthritis; Medical Research Council; National Institutes of Health; Canadian Institutes of Health Research; National Institute of General Medical Sciences; National Institute for Health and Care Research; National Human Genome Research Institute; Wellcome Trust","keywords":"Imputation (statistics); Biology; Haplotype; Single-nucleotide polymorphism; Minor allele frequency; Genetics; 1000 Genomes Project; Genotype; Genome-wide association study; Genetic association; Allele frequency; Haplotype estimation; Computational biology; Missing data; Gene; Statistics; Mathematics","score_opus":0.021740057279643565,"score_gpt":0.2946708452845418,"score_spread":0.27293078800489823,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2511515754","genre_codex":"dataset","genre_gemma":"methods","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"methods","genre_consensus":null,"domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.112930164,0.0037455019,0.2694442,0.0009434028,0.00055838877,0.0011949666,0.58810216,0.0040812353,0.018999958],"genre_scores_gemma":[0.15483217,0.0013072311,0.13565473,0.0008171925,0.00017568914,0.0018579704,0.69259983,0.00084261934,0.011912536],"study_design_codex":"design_other","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99692506,0.0009894243,0.0004090827,0.0009901327,0.00050870155,0.00017763057],"domain_scores_gemma":[0.9927389,0.0018519529,0.0004224069,0.0030765727,0.0016802499,0.0002299144],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0063798274,0.0009618212,0.0019009155,0.0035774102,0.00097341667,0.0015457422,0.0017270944,0.0015106357,0.03402873],"category_scores_gemma":[0.016401017,0.00089388713,0.0013312021,0.006110421,0.00025333045,0.0007321132,0.0010132336,0.0015373923,0.020946622],"study_design_candidate":"bench_or_experimental","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.002772889,0.00093025493,0.12967587,0.0016519964,0.004042144,0.0019098361,0.0010789374,0.016607396,0.039594278,0.008408862,0.32707155,0.46625602],"study_design_scores_gemma":[0.002521774,0.00081606896,0.32664606,0.0015289625,0.0041520507,0.005253151,0.00041675597,0.019387336,0.01457067,0.025943248,0.5984801,0.00028390597],"about_ca_topic_score_codex":0.006647231,"about_ca_topic_score_gemma":0.008089233,"teacher_disagreement_score":0.03402873,"about_ca_system_score_codex":0.00031852903,"about_ca_system_score_gemma":0.0020375738,"threshold_uncertainty_score":0.11383748},"labels":[],"label_agreement":null},{"id":"W2514286461","doi":"10.1038/ng.3661","title":"Mutations in SNORD118 cause the cerebral microangiopathy leukoencephalopathy with calcifications and cysts","year":2016,"lang":"en","type":"article","venue":"Nature Genetics","topic":"RNA modifications and cancer","field":"Biochemistry, Genetics and Molecular Biology","cited_by":147,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Alberta Children's Hospital; BC Cancer Agency","funders":"National Heart, Lung, and Blood Institute; College of Pharmacy, University of Michigan; National Institute of Neurological Disorders and Stroke; Centre National de la Recherche Scientifique; University of Michigan; Agence Nationale de la Recherche; Biotechnology and Biological Sciences Research Council; Great Ormond Street Hospital Charity; Newlife the Charity for Disabled Children; Wellcome Trust","keywords":"Biology; Small nucleolar RNA; Leukoencephalopathy; Ribosome biogenesis; Phenotype; Genetics; Mutation; Transcriptome; Ribosomal protein; Ribosome; Gene; Gene expression; Pathology; Disease; Non-coding RNA; RNA","score_opus":0.007472872628438752,"score_gpt":0.24905594499255687,"score_spread":0.2415830723641181,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2514286461","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9942655,0.00060100696,0.001599739,0.00030063977,0.00015398793,0.000017179977,0.00041587683,0.0001507225,0.002495366],"genre_scores_gemma":[0.9973072,0.00018818906,0.0009158531,0.000056582576,0.00004977524,0.0000047955077,0.00020224444,0.000050071376,0.0012252312],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9997855,0.000025104162,0.000025795302,0.00003588735,0.00010068601,0.000027065076],"domain_scores_gemma":[0.99958426,0.00011186198,0.0001400183,0.000021428723,0.00003144365,0.00011102958],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00011237203,0.0011893122,0.00039162845,0.00068747764,0.00030992395,0.0004170905,0.00042197658,0.0013019615,0.0018153258],"category_scores_gemma":[0.00067637186,0.00022205169,0.00033883326,0.0004456836,0.00048744178,0.0001966081,0.00035823032,0.00048653356,0.0004897047],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0014625792,0.00018724299,0.026161214,0.00016321425,0.00024001171,0.13060205,0.0002800124,0.0016197609,0.8072915,0.0025665518,0.003055795,0.026370056],"study_design_scores_gemma":[0.0006706682,0.0008701373,0.20556286,0.0001783868,0.00057556457,0.28020743,0.00058666366,0.012446054,0.46598893,0.005817916,0.026910739,0.00018461845],"about_ca_topic_score_codex":0.001309143,"about_ca_topic_score_gemma":0.0023234542,"teacher_disagreement_score":0.0018153258,"about_ca_system_score_codex":0.00032819636,"about_ca_system_score_gemma":0.0002094395,"threshold_uncertainty_score":0.0060728192},"labels":[],"label_agreement":null},{"id":"W2514448720","doi":"10.1038/ng.3646","title":"Lineage-specific and single-cell chromatin accessibility charts human hematopoiesis and leukemia evolution","year":2016,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Acute Myeloid Leukemia Research","field":"Medicine","cited_by":1292,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Princess Margaret Cancer Centre; University Health Network","funders":"U.S. National Library of Medicine; National Cancer Institute; National Institute of Arthritis and Musculoskeletal and Skin Diseases; National Human Genome Research Institute; Howard Hughes Medical Institute","keywords":"Biology; Chromatin; Haematopoiesis; Stem cell; Lineage (genetic); Genetics; Hematopoietic stem cell; Leukemia; Computational biology; Enhancer; Myeloid; Epigenomics; Cancer research; Gene; Transcription factor; DNA methylation; Gene expression","score_opus":0.020556927895503726,"score_gpt":0.2904839785553225,"score_spread":0.26992705065981876,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2514448720","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.995484,0.0007926791,0.0019487755,0.000031775875,0.0000032394396,0.0000044217168,0.0003967145,0.000019709423,0.0013186929],"genre_scores_gemma":[0.9980124,0.00032660426,0.0006225863,0.000016473932,0.0000038504013,0.0000035695055,0.000267207,0.000017083357,0.000730216],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.999859,0.00002635399,0.000007886557,0.000051806237,0.00003054438,0.000024496145],"domain_scores_gemma":[0.9995702,0.00018055223,0.00007352149,0.00006385886,0.0000671807,0.000044711633],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0003702187,0.00006241333,0.00020170146,0.00075761083,0.00018960745,0.00057127705,0.0002184713,0.000199322,0.0018704642],"category_scores_gemma":[0.00081017305,0.00017819653,0.00013199075,0.00066955783,0.00028649112,0.00038040854,0.00034517323,0.00025840374,0.0002464776],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00024441187,0.000014853233,0.16086484,0.00006442728,0.00006829067,0.0001046583,0.0010441521,0.0015795646,0.7937467,0.00342087,0.00021252903,0.0386347],"study_design_scores_gemma":[0.0000061932806,0.000075002514,0.9349557,0.000012064788,0.000037934646,0.000541618,0.00044560185,0.0034927176,0.053697612,0.0019785527,0.004737467,0.000019463701],"about_ca_topic_score_codex":0.0016415579,"about_ca_topic_score_gemma":0.004460124,"teacher_disagreement_score":0.0018704642,"about_ca_system_score_codex":0.00033164865,"about_ca_system_score_gemma":0.00012838212,"threshold_uncertainty_score":0.0062572956},"labels":[],"label_agreement":null},{"id":"W2519445944","doi":"10.1038/ng.3667","title":"The genetics of blood pressure regulation and its target organs from association studies in 342,415 individuals","year":2016,"lang":"en","type":"review","venue":"Nature Genetics","topic":"Genetic Associations and Epidemiology","field":"Biochemistry, Genetics and Molecular Biology","cited_by":438,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Canadian Heart Research Centre","funders":"Eunice Kennedy Shriver National Institute of Child Health and Human Development; National Center for Research Resources; National Institute of Diabetes and Digestive and Kidney Diseases; National Center for Advancing Translational Sciences; Wellcome Trust; National Human Genome Research Institute; National Eye Institute; National Institute on Aging; Fogarty International Center; National Heart, Lung, and Blood Institute; National Institute of Mental Health; Medical Research Council; Versus Arthritis; National Institute of Neurological Disorders and Stroke; National Institute of General Medical Sciences; National Institute for Health and Care Research; National Institutes of Health; National Institute of Environmental Health Sciences; Lundbeckfonden; National Cancer Institute; British Heart Foundation","keywords":"Biology; Single-nucleotide polymorphism; Genome-wide association study; Blood pressure; SNP; Genetic association; Genotype; Genetics; Genetic architecture; Internal medicine; Bioinformatics; Quantitative trait locus; Endocrinology; Gene; Medicine","score_opus":0.023287362777063732,"score_gpt":0.33097677261584924,"score_spread":0.3076894098387855,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2519445944","genre_codex":"review","genre_gemma":"review","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"review","genre_consensus":"review","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.000325966,0.9982377,0.0002848404,0.0004137919,0.00010509136,0.000004364353,0.000049379123,0.000006653676,0.00057219254],"genre_scores_gemma":[0.0018748139,0.9971764,0.00028277218,0.00019332443,0.00014500335,0.0000061754467,0.00008476592,0.0000021159742,0.00023466842],"study_design_codex":"design_other","study_design_gemma":"meta_analysis","domain_scores_codex":[0.9994282,0.00012230786,0.00010766593,0.00012553735,0.0001837586,0.000032447293],"domain_scores_gemma":[0.9986255,0.00084869144,0.00017022865,0.000040916133,0.00025524318,0.00005936877],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0018239495,0.0010095831,0.0018656958,0.003262364,0.00022386093,0.0010431644,0.0009979032,0.0011276708,0.0020736381],"category_scores_gemma":[0.0022422043,0.0003188216,0.0008320295,0.002944124,0.000705215,0.0007440577,0.00076960307,0.0014895919,0.0010555369],"study_design_candidate":"meta_analysis","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00013491999,0.000030413259,0.0032654782,0.0121264765,0.00058113487,0.0004202629,0.00006693141,0.00024044246,0.0009426567,0.0023310552,0.010324663,0.9695356],"study_design_scores_gemma":[0.000089575035,0.0002450108,0.03806494,0.016423462,0.0028570155,0.010760661,0.00020414003,0.00032746192,0.0019164145,0.01052317,0.91845685,0.00013137214],"about_ca_topic_score_codex":0.001721373,"about_ca_topic_score_gemma":0.002784152,"teacher_disagreement_score":0.003262364,"about_ca_system_score_codex":0.0007400936,"about_ca_system_score_gemma":0.0014468741,"threshold_uncertainty_score":0.009646058},"labels":[],"label_agreement":null},{"id":"W2519483107","doi":"10.1038/ng.3654","title":"Trans-ancestry meta-analyses identify rare and common variants associated with blood pressure and hypertension","year":2016,"lang":"en","type":"review","venue":"Nature Genetics","topic":"Genetic Associations and Epidemiology","field":"Biochemistry, Genetics and Molecular Biology","cited_by":330,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Janeway Children's Health and Rehabilitation Centre","funders":"National Cancer Institute; National Institute on Drug Abuse; National Heart, Lung, and Blood Institute; NIHR Cambridge Biomedical Research Centre; National Center for Advancing Translational Sciences; Medical Research Council; College of Pharmacy, University of Michigan; National Institutes of Health; Novo Nordisk Fonden; Tartu Ülikool; Erasmus Medisch Centrum; National Human Genome Research Institute; International Centre for Diarrhoeal Disease Research, Bangladesh; Eunice Kennedy Shriver National Institute of Child Health and Human Development; ZonMw; School of Medicine, Boston University; European Commission; National Institute of Mental Health; Hrvatska Zaklada za Znanost; University of Edinburgh; National Institute on Aging; Centre for Cognitive Ageing and Cognitive Epidemiology; National Institute for Health and Care Research; Scottish Government; U.S. National Library of Medicine; National Institute of Neurological Disorders and Stroke; British Heart Foundation; Norwegian Institute of Public Health; Nederlandse Organisatie voor Wetenschappelijk Onderzoek; Biotechnology and Biological Sciences Research Council; Wellcome Trust; Directorate for Biological Sciences; Imperial College London; Foundation for Cardiovascular Research; Lundbeckfonden; Age UK; European Regional Development Fund; Università degli Studi di Verona; University of Michigan; Home Office; Sydäntutkimussäätiö; National Institute of Diabetes and Digestive and Kidney Diseases; Norges Teknisk-Naturvitenskapelige Universitet; Pfizer","keywords":"Biology; Blood pressure; Meta-analysis; Genetics; Bioinformatics; Computational biology; Internal medicine; Endocrinology; Medicine","score_opus":0.08923140493814373,"score_gpt":0.37220723423136637,"score_spread":0.2829758292932226,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2519483107","genre_codex":"review","genre_gemma":"review","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"review","genre_consensus":"review","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.0013269569,0.9966364,0.00047869136,0.0008129383,0.00019245029,0.000004450731,0.00018231882,0.00001082965,0.0003548942],"genre_scores_gemma":[0.014955699,0.9815066,0.0012310022,0.0010882277,0.00056327734,0.000015329391,0.00029953514,0.000008264919,0.0003320781],"study_design_codex":"design_other","study_design_gemma":"meta_analysis","domain_scores_codex":[0.9993179,0.00019771345,0.00012283615,0.00018143361,0.00013645629,0.000043754113],"domain_scores_gemma":[0.99779236,0.0016656122,0.00023418674,0.00008023298,0.00016779546,0.000059741225],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0022513813,0.0011281859,0.0023143357,0.0012381243,0.00015520582,0.001141139,0.0011088158,0.0013496939,0.0023465648],"category_scores_gemma":[0.004659082,0.0003894078,0.0021357292,0.002297724,0.00038659226,0.0006799984,0.000864126,0.0015318547,0.0003302557],"study_design_candidate":"meta_analysis","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0015113427,0.00006834048,0.027666124,0.049285576,0.034100756,0.0011651701,0.00018103633,0.0010780024,0.0014679013,0.0042040055,0.027353685,0.851918],"study_design_scores_gemma":[0.0012580404,0.000656738,0.13551521,0.03978091,0.17833169,0.008778213,0.000645499,0.001461585,0.0021002183,0.038521726,0.592634,0.00031623017],"about_ca_topic_score_codex":0.0021659918,"about_ca_topic_score_gemma":0.006863804,"teacher_disagreement_score":0.0023465648,"about_ca_system_score_codex":0.00037222193,"about_ca_system_score_gemma":0.0011610576,"threshold_uncertainty_score":0.011906624},"labels":[],"label_agreement":null},{"id":"W2519713790","doi":"10.1038/ng.3658","title":"Unsupervised detection of cancer driver mutations with parsimony-guided learning","year":2016,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Cancer Genomics and Diagnostics","field":"Biochemistry, Genetics and Molecular Biology","cited_by":58,"is_retracted":false,"has_abstract":false,"route_ca_aff":false,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"","funders":"U.S. National Library of Medicine; Canadian Institutes of Health Research","keywords":"Cancer; Biology; Mutation; Computational biology; Set (abstract data type); Computer science; Machine learning; Artificial intelligence; Genetics; Gene","score_opus":0.005864012174068114,"score_gpt":0.24991111048130568,"score_spread":0.24404709830723756,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2519713790","genre_codex":"methods","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":null,"domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.24753836,0.0010923228,0.74246013,0.0008006033,0.00006686025,0.00020083907,0.0014983801,0.004781341,0.0015610984],"genre_scores_gemma":[0.7504455,0.000206358,0.24176298,0.00041763534,0.00008690462,0.00019156185,0.0047597443,0.00044972,0.0016796632],"study_design_codex":"design_other","study_design_gemma":"simulation_or_modeling","domain_scores_codex":[0.9983352,0.00062406115,0.000115522525,0.00044587816,0.00031213398,0.00016715586],"domain_scores_gemma":[0.9925525,0.0057255668,0.00042495248,0.0005726263,0.00050415006,0.0002201158],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0025506916,0.0012493802,0.0017932934,0.0026752506,0.0011114839,0.0012293602,0.0033207498,0.0024214988,0.0018315502],"category_scores_gemma":[0.0076902453,0.0008362939,0.0015887975,0.0018525047,0.0010969767,0.0014360155,0.0019766195,0.002563686,0.0010382091],"study_design_candidate":"simulation_or_modeling","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0021416477,0.0007125681,0.024650732,0.0005355218,0.00069887075,0.00082850095,0.00041830557,0.43211874,0.032147385,0.009035935,0.0092523,0.4874594],"study_design_scores_gemma":[0.000048259426,0.000075706266,0.0010164004,0.000012997163,0.000043772867,0.00011060524,0.000024778792,0.9888831,0.002394704,0.00697099,0.00040506976,0.00001358911],"about_ca_topic_score_codex":0.0027602043,"about_ca_topic_score_gemma":0.006004321,"teacher_disagreement_score":0.0033207498,"about_ca_system_score_codex":0.00069574977,"about_ca_system_score_gemma":0.0016879106,"threshold_uncertainty_score":0.013489485},"labels":[],"label_agreement":null},{"id":"W2529032957","doi":"10.1038/ng.3693","title":"Association of host genome with intestinal microbial composition in a large healthy cohort","year":2016,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Gut microbiota and health","field":"Biochemistry, Genetics and Molecular Biology","cited_by":486,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Wilfrid Laurier University; Izaak Walton Killam Health Centre; University of Calgary; Sinai Health System; Mount Sinai Hospital; Lunenfeld-Tanenbaum Research Institute; Hospital for Sick Children; Public Health Ontario; University of Toronto","funders":"Canadian Institutes of Health Research","keywords":"Biology; Genome-wide association study; Microbiome; Single-nucleotide polymorphism; Eubacterium; Genetics; Feces; Cohort; Gut flora; Microbial genetics; Genetic association; Gene; Immunology; Genotype; Ecology; Internal medicine; Bacteria; Medicine","score_opus":0.0031831503701951606,"score_gpt":0.24055663494856236,"score_spread":0.2373734845783672,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2529032957","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9992034,0.00013174208,0.00016069357,0.00004366249,0.000008083822,0.0000032796338,0.00026553866,0.000005849167,0.00017787989],"genre_scores_gemma":[0.9992366,0.00005408452,0.00013376515,0.00004208272,0.000012720134,0.0000059645936,0.00019223167,0.000008026743,0.0003145204],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99928635,0.00017792232,0.000038634047,0.0003113606,0.000060043887,0.00012578798],"domain_scores_gemma":[0.9991086,0.00018429982,0.00018175908,0.00018772378,0.000066818895,0.000270743],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.000554058,0.00046910037,0.00048182215,0.00068632705,0.0010860674,0.0008542935,0.00056521833,0.00084124395,0.0027135063],"category_scores_gemma":[0.001412345,0.0005771033,0.0007396265,0.0008886839,0.0006020089,0.00043372184,0.0008245301,0.0009352138,0.00027496304],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00069369597,0.000072176146,0.99251306,0.000010834182,0.0003229276,0.00035315187,0.00020815621,0.000044702967,0.004521611,0.00006803348,0.00020894203,0.000982764],"study_design_scores_gemma":[0.000019509187,0.00013085295,0.99857104,0.0000032278494,0.00010989791,0.00041872982,0.00019012648,0.0001513629,0.00014440312,0.00005901527,0.0001956946,0.000006135865],"about_ca_topic_score_codex":0.00690189,"about_ca_topic_score_gemma":0.0064542363,"teacher_disagreement_score":0.00690189,"about_ca_system_score_codex":0.00021187526,"about_ca_system_score_gemma":0.00030636837,"threshold_uncertainty_score":0.013723433},"labels":[],"label_agreement":null},{"id":"W2531660572","doi":"10.1038/ng.3688","title":"The genomic landscape of schwannoma","year":2016,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Neurofibromatosis and Schwannoma Cases","field":"Medicine","cited_by":188,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Toronto; SickKids Foundation; Hospital for Sick Children; Princess Margaret Cancer Centre; University Health Network","funders":"Canadian Institutes of Health Research","keywords":"Biology; Cancer research; Carcinogenesis; Fusion gene; Exome; DNA methylation; Exome sequencing; Schwannoma; MAPK/ERK pathway; Genetics; Mutation; Gene; Pathology; Gene expression; Signal transduction; Medicine","score_opus":0.009866244668198375,"score_gpt":0.25212801746064367,"score_spread":0.2422617727924453,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2531660572","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.96994007,0.005964416,0.0014238516,0.006785788,0.000051408926,0.000012478272,0.000664591,0.000047282185,0.015110127],"genre_scores_gemma":[0.9968732,0.0015401216,0.0003915584,0.00033492464,0.00010615211,0.000004140589,0.0002072228,0.0000102061385,0.00053252827],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9997271,0.00006116304,0.000015263355,0.000068122936,0.000062963656,0.00006547052],"domain_scores_gemma":[0.9995622,0.00022344493,0.00009024453,0.000027227316,0.000043027787,0.00005394377],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00018512282,0.00018762221,0.00019182671,0.0014869594,0.00052950066,0.0008515327,0.00034390338,0.0007339973,0.0033804078],"category_scores_gemma":[0.001429384,0.0001497547,0.00014149457,0.0012663159,0.0005978588,0.0006637802,0.0005502499,0.0003584322,0.0003114004],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0012409618,0.00018943162,0.5782212,0.00042145766,0.00028797024,0.06698201,0.0031499008,0.005943262,0.12106162,0.042005118,0.007887435,0.17260963],"study_design_scores_gemma":[0.00005019608,0.0002862544,0.77155143,0.00024589678,0.00043206633,0.09143743,0.0042352783,0.004142583,0.011406243,0.0736217,0.042524967,0.00006594124],"about_ca_topic_score_codex":0.0012856158,"about_ca_topic_score_gemma":0.001402839,"teacher_disagreement_score":0.0033804078,"about_ca_system_score_codex":0.0003876034,"about_ca_system_score_gemma":0.00029656183,"threshold_uncertainty_score":0.01130861},"labels":[],"label_agreement":null},{"id":"W2535017817","doi":"10.1038/ng.3691","title":"Deregulation of DUX4 and ERG in acute lymphoblastic leukemia","year":2016,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Acute Lymphoblastic Leukemia research","field":"Medicine","cited_by":318,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Princess Margaret Cancer Centre; University of Toronto; University Health Network","funders":"National Institute of General Medical Sciences; National Cancer Institute; National Institutes of Health","keywords":"Erg; Biology; Transactivation; ETS transcription factor family; Transcription factor; Gene isoform; Transcription (linguistics); Cancer research; Molecular biology; Exon; Genetics; Gene","score_opus":0.008064641672652197,"score_gpt":0.27644081409479604,"score_spread":0.26837617242214384,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2535017817","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9929255,0.0029322798,0.00094575115,0.00037488373,0.00003810919,0.000009133375,0.00031630605,0.00005240179,0.0024056365],"genre_scores_gemma":[0.99685836,0.00089561223,0.00036953663,0.00007504027,0.000012801663,0.0000057342086,0.00025401392,0.000017030341,0.0015117702],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9997714,0.00007023825,0.000018802242,0.000029094725,0.00005780617,0.00005259102],"domain_scores_gemma":[0.9998117,0.00006048384,0.000055583714,0.00002001987,0.00001530768,0.000037034435],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00024690593,0.0002787019,0.000279842,0.0007756053,0.00022302964,0.00058631925,0.00032499712,0.0004967007,0.0031897998],"category_scores_gemma":[0.00048810552,0.00019396885,0.00025346215,0.00043093282,0.0003694989,0.00026187504,0.00036079687,0.0003333363,0.0004110415],"study_design_candidate":"bench_or_experimental","study_design_consensus":"bench_or_experimental","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0031183073,0.00015704452,0.10169028,0.00023094793,0.0002622617,0.00831534,0.00022801233,0.0032432983,0.8330509,0.0055737947,0.001583604,0.042546164],"study_design_scores_gemma":[0.00037288317,0.00052773656,0.5132382,0.00009484824,0.00053529674,0.036031667,0.00093857315,0.009636148,0.3969304,0.006733863,0.034899727,0.000060699105],"about_ca_topic_score_codex":0.0009899682,"about_ca_topic_score_gemma":0.0009839166,"teacher_disagreement_score":0.0031897998,"about_ca_system_score_codex":0.0005372083,"about_ca_system_score_gemma":0.00027034638,"threshold_uncertainty_score":0.01067096},"labels":[],"label_agreement":null},{"id":"W2538851899","doi":"10.1038/ng.3685","title":"Genome-wide association analyses identify new susceptibility loci for oral cavity and pharyngeal cancer","year":2016,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Oral Health Pathology and Treatment","field":"Dentistry","cited_by":252,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Lunenfeld-Tanenbaum Research Institute; Mount Sinai Hospital; Princess Margaret Cancer Centre","funders":"National Institute of Environmental Health Sciences; National Cancer Institute; Medical Research Council; National Institute for Health and Care Research; World Health Organization","keywords":"Biology; Genetics; Genome-wide association study; Genome; Cancer; Oral cavity; Computational biology; Single-nucleotide polymorphism; Evolutionary biology; Genotype; Gene","score_opus":0.05031617112055349,"score_gpt":0.4181700811593038,"score_spread":0.36785391003875034,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2538851899","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99524385,0.001700353,0.0012879336,0.00031764322,0.000035733738,0.000008901865,0.00043772935,0.000041067193,0.0009268135],"genre_scores_gemma":[0.99775237,0.00050460285,0.0009035133,0.000063281426,0.00003685228,0.0000064290557,0.00025151562,0.000022432207,0.0004590111],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9992687,0.00018707932,0.000072588526,0.00021658698,0.00014461899,0.00011043576],"domain_scores_gemma":[0.99851507,0.00070764497,0.00041297634,0.00012228425,0.000089971516,0.00015207741],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0008611386,0.0006086363,0.00042649603,0.0021013753,0.00057448354,0.0010682564,0.0006668599,0.0010958194,0.0037476541],"category_scores_gemma":[0.0020420786,0.0005024775,0.0013860995,0.0021628148,0.0006121341,0.0003643576,0.000650931,0.0009947427,0.00031742465],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0026354669,0.0002453311,0.9011123,0.00013217906,0.0021606993,0.0025665879,0.00043282102,0.00043122243,0.06744968,0.000711553,0.0009968103,0.021125343],"study_design_scores_gemma":[0.00009326819,0.00011369627,0.9927838,0.00001629824,0.0007944541,0.0016705529,0.00021336478,0.0007058582,0.0021310917,0.0005731482,0.000886202,0.000018179104],"about_ca_topic_score_codex":0.0031792463,"about_ca_topic_score_gemma":0.0047114547,"teacher_disagreement_score":0.0037476541,"about_ca_system_score_codex":0.00022260581,"about_ca_system_score_gemma":0.00033122432,"threshold_uncertainty_score":0.012537122},"labels":[],"label_agreement":null},{"id":"W2544696205","doi":"10.1038/ng.3704","title":"Mycobacterium tuberculosis lineage 4 comprises globally distributed and geographically restricted sublineages","year":2016,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Tuberculosis Research and Epidemiology","field":"Medicine","cited_by":481,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Public Health Ontario","funders":"National Institute of Allergy and Infectious Diseases; Francis Crick Institute; Wellcome Trust; National Natural Science Foundation of China; Universität Basel; Deutsches Zentrum für Infektionsforschung; National Institutes of Health; Schweizerischer Nationalfonds zur Förderung der Wissenschaftlichen Forschung; Novartis Foundation; SystemsX.ch; World Health Organization; National Science Foundation","keywords":"Generalist and specialist species; Biology; Lineage (genetic); Obligate; Mycobacterium tuberculosis; Tuberculosis; Population; Evolutionary biology; Niche; Genetics; Gene; Ecology; Demography","score_opus":0.012642855802479697,"score_gpt":0.29900792241885615,"score_spread":0.28636506661637645,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2544696205","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.998804,0.00030278674,0.00030508442,0.000036798083,0.0000019653091,0.00000581297,0.00016187142,0.000006689233,0.0003749279],"genre_scores_gemma":[0.99797183,0.00033600436,0.0007004763,0.00006726936,0.0000100183315,0.000008310147,0.0006407505,0.000010449435,0.0002549207],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9996369,0.00007318731,0.000028089871,0.00013603384,0.000042313797,0.0000834352],"domain_scores_gemma":[0.9995493,0.00009101259,0.00019161907,0.000064384636,0.00005913565,0.000044489952],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00037643596,0.00035716366,0.00043415453,0.001200476,0.00037573703,0.0005960168,0.0001910256,0.00040351518,0.00096168194],"category_scores_gemma":[0.0008203932,0.00020046634,0.00030002682,0.0010760619,0.0003341782,0.0003531185,0.00062586245,0.0003094489,0.0002839643],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00049706525,0.00002981005,0.8969543,0.000053143987,0.00018583355,0.0006152368,0.0010372003,0.0003861287,0.07678558,0.00019096537,0.00042279527,0.022842031],"study_design_scores_gemma":[0.000024489975,0.00016701772,0.98794067,0.000029541956,0.00012402509,0.0026666457,0.0007970417,0.000538258,0.0032408016,0.000470238,0.0039854045,0.000015811645],"about_ca_topic_score_codex":0.0021114945,"about_ca_topic_score_gemma":0.0037698755,"teacher_disagreement_score":0.0021114945,"about_ca_system_score_codex":0.00023205209,"about_ca_system_score_gemma":0.00015398278,"threshold_uncertainty_score":0.004198432},"labels":[],"label_agreement":null},{"id":"W2551102722","doi":"10.1038/ng.3725","title":"Contribution of copy number variants to schizophrenia from a genome-wide study of 41,321 subjects","year":2016,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Genomic variations and chromosomal abnormalities","field":"Biochemistry, Genetics and Molecular Biology","cited_by":1142,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Toronto; Centre for Addiction and Mental Health; Hospital for Sick Children","funders":"National Human Genome Research Institute; Stanley Center for Psychiatric Research, Broad Institute; National Institute of Mental Health; Medical Research Council; National Institute for Health and Care Research; Lundbeckfonden; Wellcome Trust","keywords":"Biology; Copy-number variation; Genetics; Schizophrenia (object-oriented programming); Genome; Genome-wide association study; Computational biology; Gene; Single-nucleotide polymorphism; Psychiatry; Genotype; Psychology","score_opus":0.004881425022436626,"score_gpt":0.23123740989948272,"score_spread":0.22635598487704608,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2551102722","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9988451,0.00023595456,0.00014335189,0.000033695444,0.000004082224,0.0000049622586,0.0005616464,0.000004478933,0.00016669792],"genre_scores_gemma":[0.9988336,0.0001776354,0.00009440815,0.00002367876,0.0000066509842,0.000006528883,0.00065746455,0.0000051768284,0.00019474541],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9993205,0.00013890208,0.00007486726,0.00024946287,0.00012481275,0.00009144742],"domain_scores_gemma":[0.99937135,0.0002625843,0.00012304356,0.00009121559,0.00006840716,0.00008338416],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00079436845,0.00060923875,0.0005968749,0.0012738906,0.00087036204,0.0007005175,0.00043022475,0.0005370127,0.0019686897],"category_scores_gemma":[0.0020736845,0.000452626,0.00073644053,0.0016611638,0.00042620662,0.0002474765,0.0005978081,0.00045588156,0.00022130263],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0016945034,0.00005427879,0.96914434,0.000070560614,0.0012615449,0.002700482,0.0010144913,0.00030451835,0.016623786,0.00013338115,0.0004085157,0.006589624],"study_design_scores_gemma":[0.00003948563,0.00006972024,0.99655116,0.000010312148,0.0005530455,0.001372036,0.00021374635,0.0001651477,0.0004425651,0.00010503926,0.00046690213,0.0000109374105],"about_ca_topic_score_codex":0.011499593,"about_ca_topic_score_gemma":0.010424893,"teacher_disagreement_score":0.011499593,"about_ca_system_score_codex":0.00030065875,"about_ca_system_score_gemma":0.0003941303,"threshold_uncertainty_score":0.022865295},"labels":[],"label_agreement":null},{"id":"W2551666886","doi":"10.1038/ng.3720","title":"The genomic landscape of balanced cytogenetic abnormalities associated with human congenital anomalies","year":2016,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Genomic variations and chromosomal abnormalities","field":"Biochemistry, Genetics and Molecular Biology","cited_by":354,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Alberta Health Services; Centre Hospitalier Universitaire Sainte-Justine; Université de Montréal; University of Calgary; Dalhousie University; Izaak Walton Killam Health Centre","funders":"National Institute of General Medical Sciences; National Institute of Mental Health; Philippe Foundation; Fonds Wetenschappelijk Onderzoek; Government of Jiangsu Province; Vlaamse regering; Ministry of Education, India; National Institutes of Health; Suzhou Key Medical Center; Eunice Kennedy Shriver National Institute of Child Health and Human Development; European Commission; Royal Society Te Apārangi; Fundação para a Ciência e a Tecnologia; March of Dimes Foundation; National Science Foundation","keywords":"Biology; Breakpoint; Genetics; Karyotype; Phenotype; Copy-number variation; Genome; Chromosome; Computational biology; Gene; Human genome; Locus (genetics); MEF2C; Medical genetics; Gene expression","score_opus":0.005045188291944336,"score_gpt":0.21125547193667768,"score_spread":0.20621028364473334,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2551666886","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9806369,0.008091697,0.0019844624,0.0020314169,0.000034500426,0.0000070704823,0.0009726821,0.000067368164,0.0061739995],"genre_scores_gemma":[0.99678123,0.0019512136,0.00040310482,0.00019559794,0.00006558124,0.0000038391877,0.00026004334,0.000014522973,0.00032487445],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99962544,0.00007507467,0.00002510335,0.000101427824,0.000105039144,0.000067848894],"domain_scores_gemma":[0.9994691,0.00022618564,0.00017269306,0.000036471556,0.000044473145,0.00005115216],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00022323345,0.00027369426,0.0004037093,0.001637196,0.00027336724,0.000942203,0.00034184929,0.0005339147,0.0031238964],"category_scores_gemma":[0.0013374309,0.00022388357,0.00016871966,0.0014194233,0.00057848834,0.00042164183,0.00056970667,0.00040535672,0.00027032834],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.002130406,0.000081157945,0.45226082,0.0003244597,0.00053382805,0.012102842,0.0005708337,0.0045872135,0.3752001,0.016655669,0.0031972826,0.13235532],"study_design_scores_gemma":[0.00006177226,0.00030765773,0.8983245,0.000089356334,0.00048405761,0.02804307,0.00094057206,0.0026815597,0.023737604,0.030327516,0.014947853,0.000054561362],"about_ca_topic_score_codex":0.0006829482,"about_ca_topic_score_gemma":0.0008675456,"teacher_disagreement_score":0.0031238964,"about_ca_system_score_codex":0.0002498297,"about_ca_system_score_gemma":0.00022956626,"threshold_uncertainty_score":0.010450542},"labels":[],"label_agreement":null},{"id":"W2558208069","doi":"10.1038/ng.3752","title":"Genetic loci associated with chronic obstructive pulmonary disease overlap with loci for lung function and pulmonary fibrosis","year":2017,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Chronic Obstructive Pulmonary Disease (COPD) Research","field":"Medicine","cited_by":442,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of British Columbia; St. Paul's Hospital; Université Laval; Institut universitaire de cardiologie et de pneumologie de Québec","funders":"National Cancer Institute; National Heart, Lung, and Blood Institute; Medical Research Council; National Institutes of Health; Wellcome Trust","keywords":"COPD; Genome-wide association study; Biology; Asthma; Locus (genetics); Pulmonary function testing; Population; Genetic association; Genetics; Single-nucleotide polymorphism; Immunology; Medicine; Internal medicine; Genotype; Gene","score_opus":0.009209419184662481,"score_gpt":0.26638877366062563,"score_spread":0.25717935447596313,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2558208069","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9946562,0.0012593066,0.001312976,0.00062524114,0.000049995466,0.000014286697,0.0002964786,0.00003597887,0.0017494162],"genre_scores_gemma":[0.99834096,0.00020676339,0.00059712626,0.00010299067,0.00008048914,0.00000873013,0.00020761737,0.00001751866,0.00043785252],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9977285,0.00069689105,0.00019744059,0.00056112773,0.00045365476,0.00036241347],"domain_scores_gemma":[0.99517125,0.0019896228,0.001602199,0.00033070342,0.00027477817,0.00063157245],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00090013444,0.0010051928,0.00079622184,0.0024959713,0.0007648668,0.0011110033,0.00086867926,0.0017213098,0.0045743873],"category_scores_gemma":[0.003529266,0.0004127322,0.0012261342,0.002423739,0.0008509556,0.00040943574,0.0011487062,0.0009412761,0.00030227404],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0016518079,0.00017954399,0.9114882,0.00013113066,0.0011808007,0.0062946347,0.00077762286,0.0005350919,0.06716918,0.001517988,0.0005862946,0.00848765],"study_design_scores_gemma":[0.00006788192,0.00010768577,0.9878648,0.000039973413,0.00041800167,0.0063403933,0.00028451788,0.0005653675,0.0022430771,0.0012045649,0.000838415,0.000025308886],"about_ca_topic_score_codex":0.0026360054,"about_ca_topic_score_gemma":0.0026459957,"teacher_disagreement_score":0.0045743873,"about_ca_system_score_codex":0.00035151467,"about_ca_system_score_gemma":0.0003933599,"threshold_uncertainty_score":0.015302837},"labels":[],"label_agreement":null},{"id":"W2559217449","doi":"10.1038/ng.3727","title":"A DNA element that remembers winter","year":2016,"lang":"en","type":"letter","venue":"Nature Genetics","topic":"Plant Molecular Biology Research","field":"Agricultural and Biological Sciences","cited_by":9,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Western University; Agriculture and Agri-Food Canada","funders":"","keywords":"Biology; Repressor; Gene silencing; PRC2; Vernalization; Genetics; Epigenetics; Arabidopsis; Gene; DNA methylation; DNA; Arabidopsis thaliana; Polycomb-group proteins; Transcription factor; Gene expression; Mutant; Histone H3","score_opus":0.020932239242859307,"score_gpt":0.2556820413119599,"score_spread":0.23474980206910057,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2559217449","genre_codex":"commentary","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":null,"domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.0018217384,0.0010746879,0.00019499774,0.96657103,0.025430465,0.000007357123,0.000033623364,0.000030632295,0.004835443],"genre_scores_gemma":[0.016263103,0.0009203704,0.00028707014,0.9374225,0.017245483,0.000020918915,0.00003766198,0.000032429863,0.027770447],"study_design_codex":"not_applicable","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9985905,0.00037240985,0.00013401885,0.00018838019,0.0003973232,0.00031730474],"domain_scores_gemma":[0.99625635,0.0020334567,0.00026807134,0.00026813932,0.00048713124,0.000686841],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0022167936,0.00052358204,0.0005454422,0.00026702418,0.004627732,0.0026824435,0.0009287812,0.03274774,0.0053263237],"category_scores_gemma":[0.014527753,0.00043851393,0.00072424754,0.00020872263,0.0033944484,0.0027615959,0.00223685,0.030815741,0.0032069187],"study_design_candidate":"bench_or_experimental","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00024003943,0.00007605928,0.0017860506,0.00006493051,0.00004386209,0.006466041,0.0014440111,0.00007085206,0.0022369365,0.011756039,0.9531007,0.022714527],"study_design_scores_gemma":[0.00013356336,0.00010444877,0.0014837458,0.00016743524,0.000039564926,0.004408909,0.0016752303,0.0001801805,0.0011069957,0.01437886,0.97627264,0.00004855888],"about_ca_topic_score_codex":0.005241153,"about_ca_topic_score_gemma":0.009589382,"teacher_disagreement_score":0.03274774,"about_ca_system_score_codex":0.002681057,"about_ca_system_score_gemma":0.002088658,"threshold_uncertainty_score":0.019452572},"labels":[],"label_agreement":null},{"id":"W2560510482","doi":"10.1038/ng.3721","title":"Disease variants alter transcription factor levels and methylation of their binding sites","year":2016,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Epigenetics and DNA Methylation","field":"Biochemistry, Genetics and Molecular Biology","cited_by":564,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Toronto; Ontario Institute for Cancer Research","funders":"Nederlandse Organisatie voor Wetenschappelijk Onderzoek; ZonMw","keywords":"Biology; DNA methylation; Genetics; Methylation; Single-nucleotide polymorphism; DNA binding site; CpG site; Expression quantitative trait loci; Quantitative trait locus; Differentially methylated regions; Transcription factor; CTCF; Genome-wide association study; Computational biology; Gene; Promoter; Gene expression; Genotype; Enhancer","score_opus":0.020968196723988655,"score_gpt":0.2761229753333763,"score_spread":0.2551547786093877,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2560510482","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99145144,0.0013364758,0.0037195403,0.00031305838,0.000120135504,0.0000089106115,0.0014427574,0.00014748368,0.001460241],"genre_scores_gemma":[0.9975235,0.00022890266,0.00070833415,0.00007813076,0.000024089308,0.0000057399993,0.00035869473,0.000047960842,0.001024512],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.99960905,0.00006898857,0.000055876313,0.00015226103,0.000059818612,0.00005405517],"domain_scores_gemma":[0.9994843,0.00018216172,0.00014778475,0.00006202742,0.00003636951,0.000087438406],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00027689664,0.0005874145,0.00042700287,0.0007211761,0.0002639128,0.00049881754,0.00035870753,0.00088313426,0.007170626],"category_scores_gemma":[0.0008248142,0.0003157417,0.0003900065,0.00054224284,0.0003859797,0.00024053275,0.00028818054,0.0006650156,0.00056230323],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0015919274,0.000069943744,0.026753522,0.000087007385,0.00038633146,0.000951856,0.00011795361,0.0004983865,0.9614544,0.0012062333,0.00044538965,0.0064370525],"study_design_scores_gemma":[0.00029341946,0.0009050475,0.39888948,0.000057806075,0.0009073905,0.012572887,0.00030086355,0.004901482,0.5666737,0.004063593,0.010330424,0.000103939565],"about_ca_topic_score_codex":0.0014870132,"about_ca_topic_score_gemma":0.0017145313,"teacher_disagreement_score":0.007170626,"about_ca_system_score_codex":0.00024648278,"about_ca_system_score_gemma":0.000106941094,"threshold_uncertainty_score":0.023988128},"labels":[],"label_agreement":null},{"id":"W2563442740","doi":"10.1038/ng.3745","title":"Genome-wide association study of primary sclerosing cholangitis identifies new risk loci and quantifies the genetic relationship with inflammatory bowel disease","year":2016,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Liver Diseases and Immunity","field":"Medicine","cited_by":382,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Toronto; Toronto Western Hospital; Hospital for Sick Children; University of Calgary","funders":"National Institute on Aging; NIHR Cambridge Biomedical Research Centre; National Institute of Diabetes and Digestive and Kidney Diseases; Instituto de Salud Carlos III; Medical Research Council; Canadian Institutes of Health Research; NIHR BioResource; Centro de Investigación Biomédica en Red de Enfermedades Hepáticas y Digestivas; Center for Individualized Medicine, Mayo Clinic; British Heart Foundation; Exzellenzclusters Entzündungsforschung; National Institute for Health and Care Research; Ministerio de Ciencia e Innovación; Kwanjeong Educational Foundation; Bundesministerium für Bildung und Forschung; Deutsche Forschungsgemeinschaft; Nederlandse Organisatie voor Wetenschappelijk Onderzoek; Wellcome Trust; NHS Blood and Transplant; Genome Canada","keywords":"Primary sclerosing cholangitis; Inflammatory bowel disease; Biology; Genome-wide association study; Allele; Locus (genetics); Ulcerative colitis; Genetics; Single-nucleotide polymorphism; SNP; Disease; Genetic association; Gastroenterology; Internal medicine; Genotype; Gene; Medicine","score_opus":0.013141061154631161,"score_gpt":0.23521336089941902,"score_spread":0.22207229974478787,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2563442740","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9969999,0.00095088757,0.0008377428,0.0002500002,0.00002720265,0.000004304552,0.00023460606,0.00002465428,0.00067057303],"genre_scores_gemma":[0.9988207,0.00024695785,0.00051875855,0.000055402834,0.000036273548,0.0000036954616,0.0001250623,0.000009589248,0.0001834731],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99879634,0.0005564317,0.000104048115,0.0002737927,0.00015899084,0.00011035345],"domain_scores_gemma":[0.9977106,0.001152135,0.0005525053,0.00026657444,0.00012478766,0.0001934992],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0010288326,0.0005639983,0.00060482987,0.0015355984,0.0005099684,0.0007716921,0.00041097408,0.00083792553,0.0018662412],"category_scores_gemma":[0.0027402292,0.00043087918,0.00090763357,0.0017331584,0.00061839505,0.0002656494,0.00052902394,0.0010331273,0.00020770777],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0012232283,0.000094505805,0.9716287,0.000042878743,0.0012694524,0.0005039784,0.00010837573,0.00026547763,0.018118624,0.00021858682,0.00028199778,0.006244026],"study_design_scores_gemma":[0.000036932946,0.00010217206,0.9966583,0.0000075756084,0.0004768693,0.00064309273,0.000070131275,0.0005888027,0.00088691374,0.00026557507,0.0002555753,0.000008079813],"about_ca_topic_score_codex":0.001952834,"about_ca_topic_score_gemma":0.0033518008,"teacher_disagreement_score":0.001952834,"about_ca_system_score_codex":0.0001775771,"about_ca_system_score_gemma":0.00024037274,"threshold_uncertainty_score":0.006243229},"labels":[],"label_agreement":null},{"id":"W2571023129","doi":"10.1038/ng.3757","title":"Impaired H3K36 methylation defines a subset of head and neck squamous cell carcinomas","year":2017,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Epigenetics and DNA Methylation","field":"Biochemistry, Genetics and Molecular Biology","cited_by":243,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Western University; University Health Network; Montreal Neurological Institute and Hospital; Princess Margaret Cancer Centre; Lawson Health Research Institute; McGill University Health Centre; McGill University","funders":"National Institute of General Medical Sciences; National Cancer Institute","keywords":"Biology; Cancer research; Carcinogenesis; Histone H3; Histone; DNA methylation; Epigenome; Chromatin; Methylation; Epigenomics; Histone methyltransferase; EZH2; Histone methylation; Genetics; Gene; Gene expression","score_opus":0.013811316981523861,"score_gpt":0.2771001320474907,"score_spread":0.2632888150659668,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2571023129","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9980323,0.00026976436,0.00032542585,0.00003223901,0.0000039316415,0.0000095833775,0.00036069794,0.000042337433,0.0009237337],"genre_scores_gemma":[0.9989635,0.00014356236,0.000117307805,0.000015256513,0.0000045631546,0.0000051101983,0.00028873008,0.0000109147495,0.0004511197],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9997999,0.000012298514,0.000014929391,0.000047706395,0.00006449593,0.000060670824],"domain_scores_gemma":[0.99979585,0.000024870747,0.00005758968,0.000046142668,0.000024479768,0.00005114596],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00012349346,0.00023707833,0.00048651386,0.00096374564,0.00035949238,0.0006064206,0.0003763877,0.00028883325,0.0021997383],"category_scores_gemma":[0.00032292996,0.00023923778,0.00023721311,0.000726769,0.00039,0.00019598035,0.00036088805,0.0002399109,0.0005483159],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0010958908,0.0000609648,0.17545499,0.000053116153,0.00008323719,0.0024700884,0.00023141537,0.0003148418,0.806558,0.00036139763,0.00063168956,0.012684356],"study_design_scores_gemma":[0.000016840486,0.00018547826,0.9250424,0.000005086136,0.00009127509,0.013265918,0.00036994685,0.00064959744,0.057711013,0.00042377636,0.002220547,0.000018061673],"about_ca_topic_score_codex":0.002932579,"about_ca_topic_score_gemma":0.0033254214,"teacher_disagreement_score":0.002932579,"about_ca_system_score_codex":0.00035217646,"about_ca_system_score_gemma":0.00025077377,"threshold_uncertainty_score":0.007358849},"labels":[],"label_agreement":null},{"id":"W2573109541","doi":"10.1038/ng.3787","title":"Genome-wide association analyses for lung function and chronic obstructive pulmonary disease identify new loci and potential druggable targets","year":2017,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Chronic Obstructive Pulmonary Disease (COPD) Research","field":"Medicine","cited_by":314,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Institut universitaire de cardiologie et de pneumologie de Québec; Université Laval; St. Paul's Hospital; University of British Columbia","funders":"National Heart, Lung, and Blood Institute; Biotechnology and Biological Sciences Research Council; Economic and Social Research Council; Medical Research Council; National Institutes of Health; Wellcome Trust","keywords":"COPD; Genome-wide association study; Biology; Odds ratio; Genetic association; Linkage disequilibrium; Obstructive lung disease; Single-nucleotide polymorphism; Biobank; Bioinformatics; Internal medicine; Genetics; Allele; Medicine; Haplotype; Gene; Genotype","score_opus":0.014537193875322483,"score_gpt":0.321932842262734,"score_spread":0.3073956483874115,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2573109541","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.94967294,0.03360337,0.0076332777,0.004683547,0.0001930547,0.000028299597,0.0017265854,0.00018146745,0.002277585],"genre_scores_gemma":[0.9911692,0.0045122216,0.0027833756,0.0004469754,0.00013975217,0.000015140694,0.0005054817,0.00003007654,0.00039766688],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9993198,0.00021155091,0.000059936505,0.00019185244,0.00012776714,0.00008909161],"domain_scores_gemma":[0.99742585,0.0016404537,0.00051276793,0.00013204975,0.00010267366,0.00018609251],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0013894686,0.0006537697,0.0011582777,0.0012100943,0.00039043298,0.0013316922,0.00060745294,0.0012110872,0.0025350703],"category_scores_gemma":[0.0029122767,0.00037313413,0.0015165551,0.001815751,0.0006595945,0.00051726925,0.0005033886,0.0013856924,0.00024428242],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.004341626,0.00044531462,0.80408275,0.0005485373,0.0062939455,0.0025868611,0.00028242797,0.002560548,0.0804024,0.002751468,0.0026139296,0.09309024],"study_design_scores_gemma":[0.000313315,0.00055060966,0.9732029,0.00008163799,0.003158725,0.0015675046,0.00019653386,0.00378269,0.007135953,0.005046288,0.0049061007,0.000057622638],"about_ca_topic_score_codex":0.001471252,"about_ca_topic_score_gemma":0.002983029,"teacher_disagreement_score":0.0025350703,"about_ca_system_score_codex":0.00032638476,"about_ca_system_score_gemma":0.000546855,"threshold_uncertainty_score":0.008480668},"labels":[],"label_agreement":null},{"id":"W2576520471","doi":"10.1038/ng.3959","title":"Genetic variation and gene expression across multiple tissues and developmental stages in a nonhuman primate","year":2017,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Cancer-related molecular mechanisms research","field":"Biochemistry, Genetics and Molecular Biology","cited_by":70,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"McGill University","funders":"National Institute of Dental and Craniofacial Research; National Center for Research Resources; National Institute of Neurological Disorders and Stroke; National Institute of Mental Health; National Institute on Aging; National Institutes of Health; Wellcome Trust","keywords":"Expression quantitative trait loci; Biology; Quantitative trait locus; Genome-wide association study; Genetics; Locus (genetics); Genetic architecture; Transcriptome; Genetic variation; Genome; Gene; Computational biology; Gene expression; Evolutionary biology; Genotype; Single-nucleotide polymorphism","score_opus":0.0094711125631632,"score_gpt":0.315479565399852,"score_spread":0.3060084528366888,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2576520471","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9982591,0.00029157533,0.00036831343,0.000023016977,0.0000015314718,0.000003581676,0.00021473475,0.000010773025,0.00082746655],"genre_scores_gemma":[0.9970018,0.00048999523,0.00090111967,0.00003514193,0.000004744364,0.00002334583,0.00036579065,0.0000397168,0.0011382018],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9998535,0.000019212732,0.000005133908,0.00007845117,0.000022724284,0.000020901018],"domain_scores_gemma":[0.99985886,0.00005364648,0.000035137862,0.000018714294,0.00001225234,0.000021292159],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00016508198,0.0001753116,0.00025723933,0.0009403707,0.0006465655,0.00044725172,0.0002886227,0.00028519228,0.0013868515],"category_scores_gemma":[0.00027493812,0.0003053658,0.00017410767,0.0006857406,0.00072408875,0.00019634471,0.00030343738,0.000343391,0.00015279383],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00093241426,0.00008759125,0.06480004,0.00008147384,0.00020753354,0.0016955744,0.0022458802,0.00065815914,0.9029169,0.001864106,0.00024880923,0.024261529],"study_design_scores_gemma":[0.000018531238,0.00042633963,0.9590691,0.000025990741,0.00019025928,0.0036359285,0.0011080033,0.0007980485,0.027533153,0.0013099657,0.0058521633,0.00003254254],"about_ca_topic_score_codex":0.0045206742,"about_ca_topic_score_gemma":0.007906847,"teacher_disagreement_score":0.0045206742,"about_ca_system_score_codex":0.00031253955,"about_ca_system_score_gemma":0.0001491583,"threshold_uncertainty_score":0.008988738},"labels":[],"label_agreement":null},{"id":"W2578261095","doi":"10.1038/ng.3762","title":"Biallelic mutations in the 3′ exonuclease TOE1 cause pontocerebellar hypoplasia and uncover a role in snRNA processing","year":2017,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Fetal and Pediatric Neurological Disorders","field":"Medicine","cited_by":104,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Hospital for Sick Children; University of Toronto; Mount Sinai Hospital","funders":"National Human Genome Research Institute; Ministero della Salute; Simons Foundation Autism Research Initiative; Eunice Kennedy Shriver National Institute of Child Health and Human Development; Broad Institute; National Institute of Neurological Disorders and Stroke; National Institute of General Medical Sciences; California Institute of Regenerative Medicine; National Institutes of Health; Yale University; University of Washington; Damon Runyon Cancer Research Foundation; Ellison Medical Foundation","keywords":"Biology; Genetics; Small nuclear RNA; Exonuclease; Mutation; Gene; RNA; Polymerase","score_opus":0.016653574494505895,"score_gpt":0.28431905009381353,"score_spread":0.26766547559930765,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2578261095","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.98982716,0.0008863275,0.004896479,0.00029692333,0.00007468421,0.000029297147,0.00070121733,0.00021149036,0.003076574],"genre_scores_gemma":[0.9944115,0.00034052174,0.0031459434,0.00008900509,0.000015568417,0.000010678242,0.00027545748,0.00007521315,0.001636127],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.999734,0.000021846972,0.000027649152,0.00007595317,0.0000995445,0.000041030948],"domain_scores_gemma":[0.9994326,0.00021012641,0.0002000044,0.00003847456,0.00002607742,0.000092673174],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00014786117,0.0008338928,0.0004309398,0.0009942473,0.00040904284,0.00048791707,0.00067662523,0.0016238528,0.0034045095],"category_scores_gemma":[0.0005620559,0.00041128157,0.00029480754,0.0004143655,0.0007247585,0.00030181443,0.00062615,0.0008640112,0.000559787],"study_design_candidate":"bench_or_experimental","study_design_consensus":"bench_or_experimental","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0006619672,0.0000935141,0.01056363,0.00017201451,0.00012360518,0.03180946,0.00024843097,0.0008568065,0.9397867,0.0013411193,0.0005597608,0.013783003],"study_design_scores_gemma":[0.00016417081,0.00023675521,0.13246763,0.00008792451,0.00028664354,0.118896,0.00043912604,0.0034955814,0.73313916,0.0023750681,0.008338831,0.00007314357],"about_ca_topic_score_codex":0.0014066965,"about_ca_topic_score_gemma":0.004060907,"teacher_disagreement_score":0.0034045095,"about_ca_system_score_codex":0.0003023882,"about_ca_system_score_gemma":0.00028218416,"threshold_uncertainty_score":0.011389196},"labels":[],"label_agreement":null},{"id":"W2581179619","doi":"10.1038/ng.3781","title":"Systematic analysis of telomere length and somatic alterations in 31 cancer types","year":2017,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Telomeres, Telomerase, and Senescence","field":"Medicine","cited_by":627,"is_retracted":false,"has_abstract":false,"route_ca_aff":false,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"","funders":"Cancer Prevention and Research Institute of Texas; University of Texas MD Anderson Cancer Center; Broad Institute; McGill University; National Cancer Institute; National Institutes of Health","keywords":"Telomere; Telomerase; Biology; ATRX; Death-associated protein 6; Telomerase reverse transcriptase; Cancer; Somatic cell; Cancer research; DNA methylation; Genetics; Molecular biology; Mutation; DNA; Gene; Gene expression; Transcription factor; Nuclear protein","score_opus":0.014530959446490372,"score_gpt":0.3177384194143332,"score_spread":0.3032074599678428,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2581179619","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9942095,0.0018046673,0.0005309073,0.000016671234,0.0000051320194,0.000018303956,0.002965869,0.000024648522,0.00042433658],"genre_scores_gemma":[0.9940461,0.001003476,0.0008150628,0.000028224109,0.0000070568276,0.000020322008,0.0036118762,0.000019228859,0.00044862498],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9994942,0.000060747963,0.000074180876,0.00016419103,0.00012602464,0.000080521655],"domain_scores_gemma":[0.99832135,0.0005185521,0.00045418282,0.0003206287,0.00024243513,0.00014288539],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00059126044,0.00017960399,0.00047492355,0.0026601118,0.00042296003,0.0004253044,0.00021797422,0.00023757367,0.0013109802],"category_scores_gemma":[0.0011747937,0.00019066276,0.0005633107,0.0020812796,0.00024742814,0.00014859116,0.000551443,0.00025852007,0.00027786667],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00290165,0.000063540356,0.6334845,0.0004763355,0.0010399978,0.0007286119,0.00028620922,0.00043347478,0.31499693,0.00017236797,0.0004888029,0.04492754],"study_design_scores_gemma":[0.000024807983,0.000244899,0.97384214,0.000025472938,0.00064136536,0.0018948574,0.00011035328,0.00026745215,0.019782254,0.00010308387,0.0030505527,0.000012825294],"about_ca_topic_score_codex":0.0013215471,"about_ca_topic_score_gemma":0.0035673282,"teacher_disagreement_score":0.0026601118,"about_ca_system_score_codex":0.00026727965,"about_ca_system_score_gemma":0.0003903068,"threshold_uncertainty_score":0.00438565},"labels":[],"label_agreement":null},{"id":"W2583911935","doi":"10.1038/ng.3774","title":"CIViC is a community knowledgebase for expert crowdsourcing the clinical interpretation of variants in cancer","year":2017,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Genomics and Rare Diseases","field":"Biochemistry, Genetics and Molecular Biology","cited_by":674,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Canada's Michael Smith Genome Sciences Centre","funders":"National Institute of General Medical Sciences; National Cancer Institute; National Institutes of Health; Generalitat de Catalunya; Ministerio de Economía y Competitividad; National Human Genome Research Institute; Bundesministerium für Bildung und Forschung; Centres de Recerca de Catalunya; Institute for Research in Biomedicine","keywords":"Crowdsourcing; Relevance (law); Interpretation (philosophy); Biology; Precision medicine; Open source; Annotation; Computational biology; Data science; Bioinformatics; Genetics; Computer science; World Wide Web; Political science; Software","score_opus":0.03310572565031396,"score_gpt":0.39305294267717605,"score_spread":0.3599472170268621,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2583911935","genre_codex":"dataset","genre_gemma":"software","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"software","genre_consensus":null,"domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.0051787156,0.0055950056,0.15987374,0.0070935762,0.0016426776,0.0026383984,0.7058399,0.03412593,0.07801204],"genre_scores_gemma":[0.02971865,0.0026630056,0.20727898,0.0030710974,0.00038598478,0.0025204069,0.7367019,0.005944018,0.011715963],"study_design_codex":"not_applicable","study_design_gemma":"not_applicable","domain_scores_codex":[0.99166554,0.0019516902,0.0010653733,0.0019512008,0.0029433018,0.00042281483],"domain_scores_gemma":[0.96492153,0.014855898,0.0017260157,0.008177748,0.008141567,0.0021773528],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.010659322,0.0018385429,0.002295993,0.016794298,0.0042297915,0.0054682554,0.0063037043,0.0054475074,0.05412276],"category_scores_gemma":[0.07494247,0.0011606866,0.0019627821,0.0126206875,0.0015272377,0.0038977654,0.011739898,0.0031019652,0.029404711],"study_design_candidate":"not_applicable","study_design_consensus":"not_applicable","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00044245512,0.00014040309,0.0030737787,0.0036481335,0.0003681806,0.00070838974,0.00087587774,0.005193033,0.002071989,0.016969193,0.8666467,0.09986189],"study_design_scores_gemma":[0.0002583454,0.000028893866,0.002242742,0.0017176376,0.00018345079,0.00024677833,0.00044782305,0.010595899,0.0015121432,0.048197165,0.9344346,0.00013447159],"about_ca_topic_score_codex":0.033130575,"about_ca_topic_score_gemma":0.05898485,"teacher_disagreement_score":0.05412276,"about_ca_system_score_codex":0.0033680415,"about_ca_system_score_gemma":0.013903674,"threshold_uncertainty_score":0.18105865},"labels":[],"label_agreement":null},{"id":"W2588412823","doi":"10.1038/ng.3790","title":"Mutations in DONSON disrupt replication fork stability and cause microcephalic dwarfism","year":2017,"lang":"en","type":"article","venue":"Nature Genetics","topic":"DNA Repair Mechanisms","field":"Biochemistry, Genetics and Molecular Biology","cited_by":113,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"SickKids Foundation; Hospital for Sick Children; University of Toronto","funders":"National Cancer Institute; Medical Research Council; King Salman Center for Disability Research; Schweizerischer Nationalfonds zur Förderung der Wissenschaftlichen Forschung; King Abdulaziz City for Science and Technology; Lister Institute of Preventive Medicine; King's College London; National Institute of General Medical Sciences; Bundesministerium für Bildung und Forschung; National Institute for Health and Care Research; Medical Research Scotland; National Science Foundation; Cancer Research UK; E-Rare; Newlife the Charity for Disabled Children","keywords":"Biology; DNA replication; Genetics; Replisome; Genome instability; Cell biology; Pre-replication complex; Dwarfism; Ter protein; DNA replication factor CDT1; Mutation; Control of chromosome duplication; DNA damage; DNA; Gene; Eukaryotic DNA replication","score_opus":0.01396416536033222,"score_gpt":0.3010778836743786,"score_spread":0.28711371831404636,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2588412823","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.97727555,0.0014169586,0.006503722,0.00088730385,0.00045641916,0.000046443358,0.0012796009,0.00042614597,0.011707832],"genre_scores_gemma":[0.9858,0.0005024998,0.0022299397,0.00013041629,0.00003129776,0.000019484178,0.00040737158,0.00016089495,0.010718124],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99964106,0.000052173953,0.00004431249,0.00009267694,0.00011390841,0.00005581904],"domain_scores_gemma":[0.9992975,0.00021802112,0.00021096173,0.000037864353,0.0000460155,0.0001895946],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00019143496,0.0011381491,0.0004484126,0.0017764566,0.0006833083,0.00054546766,0.00064772845,0.0011276137,0.006960562],"category_scores_gemma":[0.00043078206,0.0003776723,0.00032498222,0.00052388204,0.0012565049,0.0003106869,0.00094658224,0.0006375582,0.0008986789],"study_design_candidate":"bench_or_experimental","study_design_consensus":"bench_or_experimental","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00043685958,0.00009531963,0.0029024517,0.00012923894,0.00007242619,0.0067244233,0.00013364863,0.0011106398,0.9774252,0.0035215083,0.0010454537,0.006402827],"study_design_scores_gemma":[0.00013087154,0.00014360069,0.010068558,0.000043638887,0.00012564998,0.0123054525,0.00032222163,0.0045164805,0.9481485,0.0014649616,0.022654284,0.00007578281],"about_ca_topic_score_codex":0.0037573837,"about_ca_topic_score_gemma":0.0060913144,"teacher_disagreement_score":0.006960562,"about_ca_system_score_codex":0.0009557556,"about_ca_system_score_gemma":0.0004977894,"threshold_uncertainty_score":0.023285449},"labels":[],"label_agreement":null},{"id":"W2590143063","doi":"10.1038/ng.3793","title":"Variant-aware saturating mutagenesis using multiple Cas9 nucleases identifies regulatory elements at trait-associated loci","year":2017,"lang":"en","type":"article","venue":"Nature Genetics","topic":"CRISPR and Genetic Engineering","field":"Biochemistry, Genetics and Molecular Biology","cited_by":118,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Université de Montréal; Montreal Heart Institute","funders":"National Institute of Diabetes and Digestive and Kidney Diseases; National Heart, Lung, and Blood Institute; National Human Genome Research Institute; Howard Hughes Medical Institute","keywords":"Biology; Genetics; Computational biology; Mutagenesis; Intergenic region; Cas9; MYB; Quantitative trait locus; Insertional mutagenesis; CRISPR; Genome; Gene; Mutation; Gene expression","score_opus":0.011847632126900706,"score_gpt":0.3017242933716994,"score_spread":0.2898766612447987,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2590143063","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.86607873,0.00069823145,0.12822345,0.00021225271,0.00006724833,0.00007580904,0.00042262123,0.0011137774,0.0031078237],"genre_scores_gemma":[0.9687176,0.00025223274,0.028120968,0.00013380888,0.0000070845,0.000023992212,0.00041015906,0.000297234,0.0020369445],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99940217,0.000053526895,0.00004158617,0.00021867827,0.00020969102,0.00007433926],"domain_scores_gemma":[0.99959284,0.0001274904,0.00009480574,0.000093300056,0.000035600944,0.000055927332],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0005104153,0.00044954914,0.00046689104,0.00038756957,0.0003156866,0.0006876811,0.0009080449,0.0005672859,0.0016364058],"category_scores_gemma":[0.00052155304,0.000440125,0.000487809,0.00027316742,0.00056808186,0.0003649533,0.00088778674,0.0012978801,0.0006112666],"study_design_candidate":"bench_or_experimental","study_design_consensus":"bench_or_experimental","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00003144905,0.00001059345,0.00022700829,0.000011441869,0.000006103738,0.00002413042,0.000007662494,0.00017099635,0.99781466,0.00022856673,0.000020813151,0.0014465702],"study_design_scores_gemma":[0.000008552426,0.00004598031,0.0017353458,0.0000032384416,0.000020541165,0.00025537345,0.000016919796,0.0046552494,0.9920191,0.0002134116,0.0010141262,0.00001206273],"about_ca_topic_score_codex":0.0011778667,"about_ca_topic_score_gemma":0.004508836,"teacher_disagreement_score":0.0016364058,"about_ca_system_score_codex":0.0006851955,"about_ca_system_score_gemma":0.0004496076,"threshold_uncertainty_score":0.005474329},"labels":[],"label_agreement":null},{"id":"W2591782339","doi":"10.1038/ng.3794","title":"Mutations in DCC cause isolated agenesis of the corpus callosum with incomplete penetrance","year":2017,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Fetal and Pediatric Neurological Disorders","field":"Medicine","cited_by":98,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Montreal Neurological Institute and Hospital; McGill University; McGill University Health Centre; Montreal Children's Hospital","funders":"National Institute of Neurological Disorders and Stroke; Agence Nationale de la Recherche","keywords":"Penetrance; Agenesis of the corpus callosum; Biology; Corpus callosum; Genetics; Phenotype; Mutation; Agenesis; Intellectual disability; Corpus Callosum Agenesis; Anatomy; Gene","score_opus":0.017468634837015325,"score_gpt":0.2720233938113319,"score_spread":0.25455475897431656,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2591782339","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9846348,0.0011339227,0.002550246,0.0010595369,0.0002107619,0.00008852407,0.0015127233,0.00025444324,0.008554948],"genre_scores_gemma":[0.9963122,0.0002641028,0.0017695389,0.00011121746,0.00007171076,0.00001805581,0.0002569009,0.00008492028,0.0011112825],"study_design_codex":"case_report","study_design_gemma":"observational","domain_scores_codex":[0.9993793,0.00005225793,0.00007011114,0.00019770974,0.0002136199,0.000086952015],"domain_scores_gemma":[0.99758863,0.0010392097,0.00056374253,0.00014316803,0.00015816561,0.0005070905],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00020041931,0.0021700696,0.00066542765,0.0020835616,0.0012411895,0.0007947736,0.001020759,0.0032005173,0.0033298968],"category_scores_gemma":[0.0023466104,0.00043456402,0.00050173973,0.0012061346,0.0025778457,0.00039319496,0.0011225017,0.0014612769,0.00063545525],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00054803665,0.00020597308,0.029088838,0.00035983,0.00023458547,0.71947753,0.0013528304,0.0024024232,0.21574707,0.003621436,0.0035633075,0.023398098],"study_design_scores_gemma":[0.00020122393,0.00020405407,0.081808075,0.00017251939,0.00027769618,0.82579553,0.00065889495,0.003101855,0.07400727,0.0018694184,0.011748936,0.000154433],"about_ca_topic_score_codex":0.0073392093,"about_ca_topic_score_gemma":0.009002791,"teacher_disagreement_score":0.0073392093,"about_ca_system_score_codex":0.001179256,"about_ca_system_score_gemma":0.0012008179,"threshold_uncertainty_score":0.014593005},"labels":[],"label_agreement":null},{"id":"W2592518050","doi":"10.1038/ng.3916","title":"Rare coding variants in PLCG2, ABI3, and TREM2 implicate microglial-mediated innate immunity in Alzheimer's disease","year":2017,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Neuroinflammation and Neurodegeneration Mechanisms","field":"Neuroscience","cited_by":1104,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Occupational Cancer Research Centre; University of Toronto","funders":"National Center for Research Resources; National Institute of Neurological Disorders and Stroke; National Institute of Diabetes and Digestive and Kidney Diseases; National Institute on Deafness and Other Communication Disorders; National Eye Institute; National Human Genome Research Institute; National Institute of Mental Health; National Heart, Lung, and Blood Institute; National Institute on Aging; National Cancer Institute; European Regional Development Fund; Bijzonder Onderzoeksfonds UGent; Instituto de Salud Carlos III; Menzies Centre for Australian Studies, King's College London, University of London; Sixth Framework Programme; University of California, Irvine; University of California, San Francisco; University of California, San Diego; University of California, Davis; University of California, Los Angeles; Genentech; National Institutes of Health; Vetenskapsrådet; Arizona Biomedical Research Commission; Fundación Ramón Areces; UK Dementia Research Institute; Instituut Born-Bunge; IXICO; Hjartavernd; Biogen; Marcus och Amalia Wallenbergs minnesfond; Generalitat de Catalunya; Universitat Autònoma de Barcelona; Ministerio de Economía y Competitividad; Erasmus Medisch Centrum; University College London Hospitals NHS Foundation Trust; Mutuelle Générale de l'Education Nationale; Academy of Finland; Servier; Swedish Brain Power; Nederlandse Organisatie voor Wetenschappelijk Onderzoek; North Bristol NHS Trust; Universiteit Antwerpen; Universidad Autónoma de Madrid; Kuopion Yliopistollinen Sairaala; Karolinska Institutet; Fonds Wetenschappelijk Onderzoek; South London and Maudsley NHS Foundation Trust; Belgian Federal Science Policy Office; National Center for Advancing Translational Sciences; Bundesministerium für Bildung und Forschung; AXA Research Fund; Ministero della Salute; H. Lundbeck A/S; Institut National de la Santé et de la Recherche Médicale; Deutsche Forschungsgemeinschaft; Cardiff University; University of Nottingham; Brigham Young University; Fondation pour la Recherche sur Alzheimer; Canadian Institutes of Health Research; European Commission; BioClinica; Newcastle University; Universitat de Barcelona; King's College London; Office of Research and Development; Parkinson's UK; Vlaamse regering; National Institute for Health and Care Research; Stichting MS Research; University of Southampton; Alzheimer's Society; Centro de Investigación Biomédica en Red sobre Enfermedades Neurodegenerativas; Agence Nationale de la Recherche; Wellcome Trust; Arizona Department of Health Services; Johns Hopkins University; Development of Innovative Strategies for a Transdisciplinary approach to ALZheimer's disease; CurePSP; Northern California Institute for Research and Education; Universität des Saarlandes; Rush University; Centro de Biología Molecular Severo Ochoa; Motor Neurone Disease Association; Novartis Pharmaceuticals Corporation; ZonMw; University of Cambridge; Stockholms Läns Landsting; University of Pittsburgh; Pfizer; EU Joint Programme – Neurodegenerative Disease Research; University of Washington; BrightFocus Foundation; Fondazione Cassa di Risparmio di Pistoia e Pescia; Alzheimer's Association; Northwestern University; Medical Research Council; Mayo Foundation for Medical Education and Research; Emory University; Universidad de Navarra; U.S. Department of Veterans Affairs; Fondation de France; University of Pennsylvania; Sanofi; Eisai; University of Southern California; U.S. Department of Defense; Hersenstichting; Eli Lilly and Company; York University; Vanderbilt University; GlaxoSmithKline; Mayo Clinic; Queen's University; University of Miami; Massachusetts General Hospital; Agence Française de Sécurité Sanitaire des Produits de Santé; Meso Scale Diagnostics; Fondation pour la Recherche Médicale; Bristol-Myers Squibb","keywords":"TREM2; Nonsynonymous substitution; Biology; Minor allele frequency; Genetics; Genome-wide association study; Microglia; Alzheimer's disease; Genotyping; Allele; Gene; Genotype; Allele frequency; Disease; Single-nucleotide polymorphism; Immunology; Genome; Immune system; Medicine; Internal medicine","score_opus":0.03495807231275978,"score_gpt":0.2946570760368707,"score_spread":0.2596990037241109,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2592518050","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9932327,0.0006270171,0.0029685874,0.00038674005,0.000053725067,0.000018538858,0.0006168127,0.00011928626,0.0019766053],"genre_scores_gemma":[0.99779654,0.00013701853,0.0012251219,0.00009838551,0.000052242285,0.000008278867,0.00017621467,0.000025950601,0.00048029772],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.99969256,0.000069837246,0.000050516144,0.00006721994,0.000080057565,0.0000397605],"domain_scores_gemma":[0.9994407,0.00021524249,0.00018536403,0.000049445796,0.00004074673,0.00006837714],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00037452043,0.00089175825,0.00033770743,0.00091360166,0.00071677996,0.0005067646,0.00042183863,0.0011954044,0.0037279052],"category_scores_gemma":[0.0009100821,0.00020407468,0.0005264821,0.00067170657,0.0006182793,0.0003194313,0.00045467075,0.0006862921,0.0004679113],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.005183122,0.00030730237,0.17898071,0.00028183358,0.0008288457,0.08871207,0.0015032578,0.0017051519,0.67672783,0.010064302,0.003167509,0.032538034],"study_design_scores_gemma":[0.0007574471,0.00071356236,0.6552594,0.0003700531,0.0019509787,0.1997907,0.001414712,0.0089765815,0.0940012,0.022445003,0.014112866,0.00020758502],"about_ca_topic_score_codex":0.0017815374,"about_ca_topic_score_gemma":0.0026694427,"teacher_disagreement_score":0.0037279052,"about_ca_system_score_codex":0.00024929002,"about_ca_system_score_gemma":0.0002243248,"threshold_uncertainty_score":0.012471139},"labels":[],"label_agreement":null},{"id":"W2593940628","doi":"10.1038/ng.3785","title":"Identification of ten variants associated with risk of estrogen-receptor-negative breast cancer","year":2017,"lang":"en","type":"article","venue":"Nature Genetics","topic":"BRCA gene mutations in cancer","field":"Biochemistry, Genetics and Molecular Biology","cited_by":471,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of British Columbia; Public Health Ontario; Simon Fraser University; McGill University; University Health Network; Hôpital du Saint-Sacrement; McGill University and Génome Québec Innovation Centre; Queen's University; Lunenfeld-Tanenbaum Research Institute; Mount Sinai Hospital; Centre Hospitalier de l’Université de Montréal; Université Laval; BC Cancer Agency; Royal Victoria Hospital; Centre hospitalier universitaire de Québec; University of Toronto","funders":"Medical Research and Materiel Command; National Institute of General Medical Sciences; National Human Genome Research Institute; National Institute of Mental Health; Erasmus Universitair Medisch Centrum Rotterdam; Instituto de Salud Carlos III; Sydney Medical School; Cancer Council Western Australia; Cancer Council NSW; Cancer Council Victoria; World Cancer Research Fund; European Social Fund; Medical Research Council; Cancer Center, University of Kansas; National Institutes of Health; Centre Léon Bérard; Hellenic Health Foundation; Freistaat Sachsen; Akershus Universitetssykehus; Liga Portuguesa Contra o Cancro; Mutuelle Générale de l'Education Nationale; Institut Gustave-Roussy; Ministero dello Sviluppo Economico; Agence Nationale de Sécurité Sanitaire de l’Alimentation, de l’Environnement et du Travail; Hospices Civils de Lyon; Cancer Council South Australia; Istituto Oncologico Veneto; Instituto Millenium; Institut National Du Cancer; Radboud Universitair Medisch Centrum; Oulun Yliopisto; National Health and Medical Research Council; Deutsche Krebshilfe; Universitair Medisch Centrum Groningen; Leids Universitair Medisch Centrum; Universitetet i Bergen; Karolinska Institutet; Associazione Italiana per la Ricerca sul Cancro; Fondation de France; Stavros Niarchos Foundation; Fisher Center for Alzheimer's Research Foundation; Peter MacCallum Cancer Centre; Kuopion Yliopistollinen Sairaala; Breast Cancer Campaign; Ministerstvo Zdravotnictví Ceské Republiky; Servicio Gallego de Salud; Institut Bergonié; Great Ormond Street Hospital for Children; Fonds Wetenschappelijk Onderzoek; Ministerio de Economía y Competitividad; Erasmus Medisch Centrum; Deutsche Gesetzliche Unfallversicherung; Nederlandse Organisatie voor Wetenschappelijk Onderzoek; King's College London; Gentofte Hospital; Cancerfonden; Cancer Australia; Radboud Universiteit; Russian Foundation for Basic Research; Norges Forskningsråd; Stockholms Läns Landsting; Universiteit Maastricht; Vrije Universiteit Amsterdam; University of Western Sydney; Maastricht Universitair Medisch Centrum; National Heart, Lung, and Blood Institute; Ohio State University; Universiteit Leiden; University of Crete; Ministero della Salute; Institut National de la Santé et de la Recherche Médicale; Medisinske fakultet, Universitetet i Oslo; Hunter Medical Research Institute; Deutscher Akademischer Austauschdienst; Robert Bosch Stiftung; Istituto Toscano Tumori; Trinity College Dublin; Agency for Science, Technology and Research; Centers for Disease Control and Prevention; Jewish General Hospital; National Institute for Health and Care Research; University of Queensland; Hungarian Scientific Research Fund; Cancer Association of South Africa; Medizinischen Hochschule Hannover; Cancer Institute NSW; Canadian Institutes of Health Research; Lietuvos Mokslo Taryba; European Commission; Deutsches Krebsforschungszentrum; University of Aberdeen; QIMR Berghofer Medical Research Institute; Fondation du cancer du sein du Québec; Génome Québec; Universitetet i Oslo; University of Nottingham; Calvary Mater Newcastle; Nottingham University Hospitals NHS Trust; National Breast Cancer Foundation; National Institute of Environmental Health Sciences; Swedish Cancer Foundation; Université Laval; Royal Marsden NHS Foundation Trust; Lon V. Smith Foundation; Vlaamse regering; Fundación Mutua Madrileña; Haukeland Universitetssjukehus; Ministère du Développement Économique, de l’Innovation et de l’Exportation; University of Southampton; Cancer Research UK; Agence Nationale de la Recherche; Wellcome Trust; David F. and Margaret T. Grohne Family Foundation; Breast Cancer Research Foundation; Generalitat de Catalunya; Univerzita Karlova v Praze; Kansas Bioscience Authority; Xunta de Galicia; Israel Cancer Association; Dr. Ralph and Marian Falk Medical Research Trust; University Hospitals of Leicester NHS Trust; National Center for Advancing Translational Sciences; Francis Crick Institute; Bundesministerium für Bildung und Forschung; Ovarian Cancer Research Fund; Odense Universitetshospital; Central Manchester University Hospitals NHS Foundation Trust; National Cancer Institute; European Regional Development Fund; Ministerio de Sanidad, Servicios Sociales e Igualdad; Government of Canada; NIHR Biomedical Research Centre, Royal Marsden NHS Foundation Trust/Institute of Cancer Research; Norges Teknisk-Naturvitenskapelige Universitet; Centre Hospitalier Universitaire de Québec; Cancer Council Tasmania; Itä-Suomen Yliopisto; Genome Canada; Institut Català de la Salut; Newcastle upon Tyne Hospitals NHS Foundation Trust; Creighton University; Institut Claudius Regaud; California Department of Public Health; Sundhed og Sygdom, Det Frie Forskningsråd; University of Washington; Massachusetts Institute of Technology; University of Toronto; University of California, San Francisco; Universitetet i Tromsø; Susan G. Komen for the Cure","keywords":"Biology; Breast cancer; Estrogen receptor; Identification (biology); Genetics; Estrogen; Estrogen receptor beta; Estrogen receptor alpha; Oncology; Internal medicine; Cancer; Computational biology; Bioinformatics; Medicine","score_opus":0.006093645637319349,"score_gpt":0.27680768873934586,"score_spread":0.2707140431020265,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2593940628","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99752,0.00044612994,0.00063856976,0.000064147505,0.00001772321,0.000016113836,0.00054923067,0.00001862691,0.00072936906],"genre_scores_gemma":[0.9982646,0.00010177777,0.000760633,0.00004028413,0.000010572072,0.000008195754,0.00046997203,0.000010656361,0.00033327818],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99936444,0.00010831662,0.00011572812,0.0001462561,0.00014959101,0.00011568134],"domain_scores_gemma":[0.9985423,0.0005980712,0.00037182233,0.00008186514,0.00012402856,0.00028188163],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00049818034,0.00061091396,0.00050326076,0.0020781276,0.00060070236,0.00063279725,0.0006128857,0.0007887302,0.0027095503],"category_scores_gemma":[0.0019982203,0.00027945515,0.0005649767,0.0017693882,0.00043181074,0.00016944452,0.0004718672,0.00043920524,0.00031483482],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0041074962,0.00025542176,0.8450837,0.00017207525,0.0007111242,0.013232367,0.0005621709,0.0009932588,0.110168345,0.0008831598,0.0007776029,0.023053234],"study_design_scores_gemma":[0.00018898287,0.0005179864,0.9551694,0.00008608603,0.0006163781,0.017023465,0.00029302304,0.0018792602,0.019844789,0.0007825394,0.0035422465,0.00005592293],"about_ca_topic_score_codex":0.0037887534,"about_ca_topic_score_gemma":0.0049758465,"teacher_disagreement_score":0.0037887534,"about_ca_system_score_codex":0.00034787916,"about_ca_system_score_gemma":0.00034024828,"threshold_uncertainty_score":0.009064317},"labels":[],"label_agreement":null},{"id":"W2601822003","doi":"10.1038/ng.3826","title":"Identification of 12 new susceptibility loci for different histotypes of epithelial ovarian cancer","year":2017,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Wheat and Barley Genetics and Pathology","field":"Agricultural and Biological Sciences","cited_by":553,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Public Health Ontario; University of British Columbia; McGill University; St. Michael's Hospital; Canada's Michael Smith Genome Sciences Centre; University Health Network; University of Toronto; Vancouver General Hospital; University of Calgary; Princess Margaret Cancer Centre; Lunenfeld-Tanenbaum Research Institute; Mount Sinai Hospital; Ovarian Cancer Canada; Université Laval; BC Cancer Agency; Women's College Hospital; Centre hospitalier universitaire de Québec","funders":"National Cancer Institute; Radboud Institute for Health Sciences; Russian Academy of Sciences; Canadian Institutes of Health Research; Knight Cancer Institute, Oregon Health and Science University; Canada's Michael Smith Genome Sciences Centre; Perelman School of Medicine, University of Pennsylvania; University of Texas MD Anderson Cancer Center; Cancer Council Victoria; Skånes universitetssjukhus; School of Medicine, Vanderbilt University; Fogarty International Center; Vanderbilt-Ingram Cancer Center; National Institutes of Health; Government of Canada; Centre Léon Bérard; Haukeland Universitetssjukehus; Radboud Universitair Medisch Centrum; Ovarian Cancer Research Fund; Háskóli Íslands; Università degli Studi di Firenze; Peter MacCallum Cancer Centre; Odense Universitetshospital; BC Cancer Agency; Karolinska Institutet; Deutsche Krebshilfe; Medizinischen Hochschule Hannover; Ministry of Earth Sciences; University of Toronto; QIMR Berghofer Medical Research Institute; Lunds Universitet; Universiteit Maastricht; Francis Crick Institute; Cedars-Sinai Medical Center; World Health Organization; Fondation du cancer du sein du Québec; Wellcome Trust; Cancer Research UK; Maastricht Universitair Medisch Centrum; Moffitt Cancer Center; Division of Cancer Epidemiology and Genetics, National Cancer Institute; Huntsman Cancer Institute; Vanderbilt University; Centre Hospitalier Universitaire de Québec; Université Laval; Helsingin Yliopisto; Genome Canada; Johns Hopkins University; Radboud Universiteit; Universitetet i Bergen; Génome Québec; University of Pennsylvania; National Institute for Health and Care Research; Massachusetts General Hospital","keywords":"Biology; Identification (biology); Epithelial ovarian cancer; Ovarian cancer; Genetics; Computational biology; Cancer; Ecology","score_opus":0.024542788091131477,"score_gpt":0.27685596335062534,"score_spread":0.25231317525949387,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2601822003","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99869835,0.000109144814,0.0006170727,0.00003578681,0.0000074448712,0.0000065891827,0.00015823558,0.000013356648,0.00035394132],"genre_scores_gemma":[0.998171,0.00008060448,0.0007397666,0.00002659869,0.000007766762,0.000008723799,0.00030901737,0.000012246504,0.000644308],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9998235,0.00003229857,0.000018012795,0.000044926448,0.000032052874,0.0000492484],"domain_scores_gemma":[0.9994843,0.00015788103,0.00015514498,0.00005199933,0.000038731316,0.000111906695],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0001745896,0.00039076756,0.00027243161,0.0012184074,0.00022991079,0.00038363817,0.00031489335,0.00034878525,0.0028998207],"category_scores_gemma":[0.00045690502,0.00025569613,0.0004006674,0.0005485383,0.00026106584,0.00012102112,0.00041255343,0.00055009284,0.00023687092],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.002220344,0.00013602682,0.121430926,0.000078276054,0.0001269797,0.0015704047,0.00032543312,0.00019925112,0.8611928,0.0006010517,0.000176171,0.011942272],"study_design_scores_gemma":[0.00017684665,0.00044575398,0.92877394,0.000022774779,0.00024439424,0.004972423,0.00038817947,0.0008000474,0.06047635,0.00064670487,0.0030284298,0.000024115809],"about_ca_topic_score_codex":0.0007782424,"about_ca_topic_score_gemma":0.0011091849,"teacher_disagreement_score":0.0028998207,"about_ca_system_score_codex":0.00020499516,"about_ca_system_score_gemma":0.00013158646,"threshold_uncertainty_score":0.009700894},"labels":[],"label_agreement":null},{"id":"W2602986494","doi":"10.1038/ng.3823","title":"Genome-wide association study of glioma subtypes identifies specific differences in genetic susceptibility to glioblastoma and non-glioblastoma tumors","year":2017,"lang":"en","type":"review","venue":"Nature Genetics","topic":"MicroRNA in disease regulation","field":"Biochemistry, Genetics and Molecular Biology","cited_by":378,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Alberta; Institute of Genetics; McGill Genome Centre; Genome Canada","funders":"National Center for Chronic Disease Prevention and Health Promotion; National Center for Research Resources; National Institute of Neurological Disorders and Stroke; National Cancer Institute; Agence Nationale de la Recherche; Wellcome Trust; University of California, San Francisco; Mayo Clinic","keywords":"Glioblastoma; Biology; Glioma; Genome-wide association study; Genetic association; Genetics; Cancer research; Single-nucleotide polymorphism; Genotype; Gene","score_opus":0.016799830065864243,"score_gpt":0.2954588668396421,"score_spread":0.2786590367737779,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2602986494","genre_codex":"review","genre_gemma":"review","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"review","genre_consensus":"review","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.00025033028,0.9981317,0.0002213873,0.0006133432,0.00027402176,0.0000033973008,0.000055935663,0.000008486116,0.00044136713],"genre_scores_gemma":[0.0016395504,0.99652547,0.00034978343,0.0005737703,0.00037554136,0.000007711997,0.000112388014,0.0000028060276,0.00041289127],"study_design_codex":"design_other","study_design_gemma":"observational","domain_scores_codex":[0.99974805,0.00004282012,0.000043233405,0.000063539715,0.00007679777,0.000025534166],"domain_scores_gemma":[0.999418,0.00029347138,0.00008539754,0.000018376804,0.00012901434,0.000055750676],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0011346553,0.0008542707,0.0015919472,0.0012119232,0.00017034732,0.00092034956,0.0009407942,0.0011397836,0.0014672406],"category_scores_gemma":[0.0011836597,0.00026864005,0.0005756253,0.001641597,0.00050566404,0.0007091772,0.0008450771,0.0016913209,0.00080358994],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0002368856,0.0000458894,0.00239039,0.0079251565,0.00045766527,0.00038298997,0.0000445732,0.00024030595,0.0020707294,0.002731311,0.035943907,0.9475303],"study_design_scores_gemma":[0.000092265436,0.0001204506,0.010941704,0.003987561,0.0009673887,0.0021408573,0.000106004314,0.00015759705,0.0010432461,0.0046220096,0.9757581,0.000062795356],"about_ca_topic_score_codex":0.0013037155,"about_ca_topic_score_gemma":0.0028247596,"teacher_disagreement_score":0.0015919472,"about_ca_system_score_codex":0.0005197391,"about_ca_system_score_gemma":0.0014684147,"threshold_uncertainty_score":0.0060006976},"labels":[],"label_agreement":null},{"id":"W2603716527","doi":"10.1038/ng.3819","title":"Natural variation at the soybean J locus improves adaptation to the tropics and enhances yield","year":2017,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Soybean genetics and cultivation","field":"Agricultural and Biological Sciences","cited_by":416,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Agriculture and Agri-Food Canada","funders":"Guangxi Academy of Agricultural Sciences; Hokkaido University; Chinese Academy of Agricultural Sciences; Chinese Academy of Sciences","keywords":"Biology; Locus (genetics); Repressor; Temperate climate; Tropics; Quantitative trait locus; Arabidopsis; Gene; Flowering Locus C; Vernalization; Trait; Adaptation (eye); Botany; Genetics; Transcription factor; Mutant; Ecology","score_opus":0.015718940146399896,"score_gpt":0.23305128202270997,"score_spread":0.21733234187631006,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2603716527","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9977926,0.00018676984,0.0006505949,0.000108833985,0.00001323315,0.0000064864175,0.00020961682,0.00006731477,0.00096450956],"genre_scores_gemma":[0.9969137,0.0002679179,0.0010718908,0.0001152871,0.000009020782,0.00000882826,0.00030725962,0.000103073886,0.001203009],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.99984694,0.000027584269,0.00001085211,0.000052828196,0.000028149441,0.000033687156],"domain_scores_gemma":[0.99976593,0.000028691502,0.00009090131,0.000014452139,0.000016959819,0.000083086954],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00021195668,0.00045171523,0.00023648707,0.00051628926,0.00020453149,0.00023320543,0.00029348445,0.00023417846,0.0018565967],"category_scores_gemma":[0.00023643994,0.0002462784,0.00019772365,0.00031049887,0.00027769821,0.00020072551,0.00049946934,0.0005391293,0.0002330243],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00018857546,0.000019673582,0.001531106,0.000015136223,0.000015779204,0.000033334374,0.00001916287,0.00008853996,0.99668235,0.00006728746,0.000047571564,0.0012914907],"study_design_scores_gemma":[0.0003854421,0.0008023935,0.59363943,0.000034130986,0.00028285536,0.0008246851,0.0005439445,0.0050193523,0.39106026,0.000615411,0.006718442,0.000073652656],"about_ca_topic_score_codex":0.0036689516,"about_ca_topic_score_gemma":0.009116376,"teacher_disagreement_score":0.0036689516,"about_ca_system_score_codex":0.0005978272,"about_ca_system_score_gemma":0.00040324026,"threshold_uncertainty_score":0.0072951913},"labels":[],"label_agreement":null},{"id":"W2604631385","doi":"10.1038/ng.3812","title":"SMARCD2 subunit of SWI/SNF chromatin-remodeling complexes mediates granulopoiesis through a CEBPɛ dependent mechanism","year":2017,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Chromatin Remodeling and Cancer","field":"Biochemistry, Genetics and Molecular Biology","cited_by":80,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Hôpital Maisonneuve-Rosemont; Université de Montréal; Institute for Research in Immunology and Cancer","funders":"","keywords":"Chromatin remodeling; Biology; SWI/SNF; Chromatin; Cell biology; Transcription factor; Protein subunit; Phenotype; Gene; Genetics","score_opus":0.0176412656441956,"score_gpt":0.29191072163209264,"score_spread":0.27426945598789704,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2604631385","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.97903156,0.0024070141,0.00924192,0.0004542211,0.00015578594,0.000051269573,0.00053952617,0.00035551263,0.0077631962],"genre_scores_gemma":[0.989202,0.00033342032,0.0018646632,0.000104569655,0.000024830175,0.000028964263,0.0007960723,0.00004833225,0.007597048],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.999785,0.000021521839,0.000012498794,0.000059737922,0.00005959203,0.00006164708],"domain_scores_gemma":[0.9998622,0.0000138354435,0.000021294787,0.00002634852,0.00002197977,0.00005429306],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00024135494,0.00045634806,0.000241847,0.00026239638,0.000371429,0.00058930705,0.00045416353,0.00039934003,0.00261373],"category_scores_gemma":[0.00024661934,0.00030800077,0.00028131437,0.00012985761,0.00034191398,0.00034032308,0.00055925926,0.00064001925,0.0016629756],"study_design_candidate":"bench_or_experimental","study_design_consensus":"bench_or_experimental","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00012077917,0.00001089416,0.0003199217,0.00001954133,0.0000051825614,0.00008832214,0.000010460738,0.000023555142,0.99819034,0.0002871572,0.00011861932,0.0008052294],"study_design_scores_gemma":[0.00002105034,0.000032268184,0.0077942745,0.0000038624576,0.0000054854836,0.00027793754,0.000024709276,0.00074178685,0.9878144,0.000100100544,0.0031802696,0.000003710404],"about_ca_topic_score_codex":0.00063451636,"about_ca_topic_score_gemma":0.00093608437,"teacher_disagreement_score":0.00261373,"about_ca_system_score_codex":0.00060112047,"about_ca_system_score_gemma":0.00028093965,"threshold_uncertainty_score":0.008743763},"labels":[],"label_agreement":null},{"id":"W2605577905","doi":"10.1038/ng.3835","title":"Genome-to-genome analysis highlights the effect of the human innate and adaptive immune systems on the hepatitis C virus","year":2017,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Hepatitis C virus research","field":"Medicine","cited_by":146,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"St. Paul's Hospital","funders":"NIHR Oxford Biomedical Research Centre; Biotechnology and Biological Sciences Research Council; Medical Research Council; National Institutes of Health; Imperial College London; National Institute of Allergy and Infectious Diseases; Alan Turing Institute; Wellcome Trust; National Institute for Health and Care Research; Gilead Sciences","keywords":"Biology; Genome; Innate immune system; Virology; Genotyping; Hepatitis C virus; Gene; Genetics; Virus; NS5A; Immune system; Genotype; Hepacivirus","score_opus":0.016948334375081975,"score_gpt":0.30637803969159527,"score_spread":0.2894297053165133,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2605577905","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.98525167,0.0035813353,0.0052345274,0.001001963,0.00007894461,0.000010129668,0.0010069292,0.00013066272,0.0037038233],"genre_scores_gemma":[0.9949062,0.0011854636,0.0022332428,0.0005381012,0.00006209478,0.0000036431768,0.0005120226,0.00006765544,0.000491646],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.99972504,0.00007940768,0.0000096354215,0.00007906687,0.00005141021,0.000055468914],"domain_scores_gemma":[0.9993901,0.00032798498,0.000075539705,0.00008375226,0.000046579782,0.000075998694],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00046238734,0.00021362014,0.0003072242,0.0005801241,0.00028034885,0.00069586514,0.0002624647,0.0004419528,0.0020171087],"category_scores_gemma":[0.00092165754,0.00013481242,0.00032081077,0.00067943387,0.00037380864,0.0003580147,0.00041286682,0.00094702916,0.00025317713],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0014297464,0.00017004382,0.096174285,0.00024902864,0.00040439225,0.001101198,0.0002346164,0.0033024384,0.790004,0.007672572,0.0021300733,0.09712753],"study_design_scores_gemma":[0.000061645536,0.0005606794,0.8530304,0.00005768452,0.00048887933,0.0025326884,0.00046370598,0.015319194,0.0864957,0.016356234,0.024572011,0.00006126265],"about_ca_topic_score_codex":0.001436642,"about_ca_topic_score_gemma":0.0018916307,"teacher_disagreement_score":0.0020171087,"about_ca_system_score_codex":0.00024147994,"about_ca_system_score_gemma":0.00027455622,"threshold_uncertainty_score":0.0067479014},"labels":[],"label_agreement":null},{"id":"W2607166912","doi":"10.1038/ng.3838","title":"Spatial heterogeneity in medulloblastoma","year":2017,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Cancer Genomics and Diagnostics","field":"Biochemistry, Genetics and Molecular Biology","cited_by":143,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of British Columbia; Ontario Institute for Cancer Research; Simon Fraser University; McGill University Health Centre; McGill University; University of Toronto; Montreal Children's Hospital; SickKids Foundation; BC Cancer Agency; Princess Margaret Cancer Centre; University Health Network; St. Michael's Hospital; Canada's Michael Smith Genome Sciences Centre; Hospital for Sick Children","funders":"Eunice Kennedy Shriver National Institute of Child Health and Human Development; National Cancer Institute; Francis Crick Institute","keywords":"Genetic heterogeneity; Transcriptome; Biology; Spatial heterogeneity; Tumour heterogeneity; Homogeneous; Somatic cell; Cancer research; Glioma; Somatic evolution in cancer; Targeted therapy; Medulloblastoma; Biopsy; Tumor heterogeneity; Computational biology; Gene; Genetics; Phenotype; Cancer; Pathology; Medicine; Gene expression","score_opus":0.00689660226055799,"score_gpt":0.27242311993906676,"score_spread":0.26552651767850877,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2607166912","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9899838,0.0020485187,0.0046656425,0.0001641849,0.000008625452,0.000007570547,0.00024389863,0.00011114212,0.0027665964],"genre_scores_gemma":[0.99871564,0.00023036827,0.0005305218,0.00000997568,0.0000069262073,0.0000045497395,0.000070637405,0.000016597562,0.00041492912],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9997414,0.000035249046,0.00001720958,0.00006627437,0.000087849956,0.00005204039],"domain_scores_gemma":[0.9994236,0.0001348062,0.00021638311,0.00008248346,0.00007860694,0.00006412286],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00029310668,0.00013766171,0.0002472668,0.0016146401,0.00035886504,0.0008811632,0.00035823626,0.00022545461,0.0013785082],"category_scores_gemma":[0.0010718339,0.000412929,0.00014966862,0.0008986172,0.0004890829,0.00062750105,0.00060525833,0.00024932713,0.00029824948],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0011876053,0.00006982027,0.22746104,0.0002483583,0.00021678698,0.002580943,0.0007187308,0.0092698485,0.6959459,0.020082252,0.0015132028,0.04070548],"study_design_scores_gemma":[0.000053640393,0.00011356689,0.8101599,0.00003018593,0.00015649229,0.01342066,0.0012482957,0.016921036,0.13240688,0.01243381,0.012993282,0.00006230458],"about_ca_topic_score_codex":0.0063330736,"about_ca_topic_score_gemma":0.006033022,"teacher_disagreement_score":0.0063330736,"about_ca_system_score_codex":0.0008299189,"about_ca_system_score_gemma":0.00031371904,"threshold_uncertainty_score":0.012592435},"labels":[],"label_agreement":null},{"id":"W2607238069","doi":"10.1038/ng.3843","title":"Large-scale analyses of common and rare variants identify 12 new loci associated with atrial fibrillation","year":2017,"lang":"en","type":"review","venue":"Nature Genetics","topic":"Atrial Fibrillation Management and Outcomes","field":"Medicine","cited_by":357,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Alberta; Hamilton Health Sciences; McMaster University; Population Health Research Institute","funders":"National Center for Advancing Translational Sciences; National Heart, Lung, and Blood Institute; National Institute of Diabetes and Digestive and Kidney Diseases; National Cancer Institute; National Institutes of Health; Wellcome Trust","keywords":"Genome-wide association study; Atrial fibrillation; Genetic association; Biology; Exome; Fibrillation; Genetics; Internal medicine; Bioinformatics; Exome sequencing; Gene; Medicine; Single-nucleotide polymorphism; Phenotype; Genotype","score_opus":0.13483505216761474,"score_gpt":0.4407118218776594,"score_spread":0.3058767697100446,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2607238069","genre_codex":"review","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":null,"domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.001653078,0.99624854,0.0004767762,0.0006124541,0.00019858088,0.0000063646007,0.00014181287,0.000013770106,0.000648555],"genre_scores_gemma":[0.0132958265,0.9835391,0.001099219,0.00093148724,0.00044653562,0.000012446923,0.00030518533,0.0000054813204,0.0003647466],"study_design_codex":"design_other","study_design_gemma":"observational","domain_scores_codex":[0.99956614,0.00006252201,0.00010417757,0.00010986148,0.0001239272,0.0000334415],"domain_scores_gemma":[0.9986865,0.00091521983,0.00022879393,0.000026973003,0.00009713852,0.000045369918],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0008916975,0.00082937855,0.0016487357,0.0015123924,0.00016033823,0.0009891853,0.0009987287,0.0010400941,0.0018729246],"category_scores_gemma":[0.0019701105,0.00022561308,0.001271697,0.0016855788,0.00038387466,0.0006139755,0.00064697483,0.0012204394,0.00040951965],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00036781366,0.00005946419,0.0146805495,0.014539656,0.0030929625,0.0015049275,0.00012332822,0.00050713384,0.0024940942,0.0019212005,0.012269966,0.948439],"study_design_scores_gemma":[0.0005190083,0.00044396074,0.1126319,0.02655629,0.021661935,0.017267281,0.00049533974,0.00070775585,0.0023408995,0.0143054025,0.8028202,0.00024999864],"about_ca_topic_score_codex":0.0011168959,"about_ca_topic_score_gemma":0.0023703058,"teacher_disagreement_score":0.0018729246,"about_ca_system_score_codex":0.00028420263,"about_ca_system_score_gemma":0.001035991,"threshold_uncertainty_score":0.0062655807},"labels":[],"label_agreement":null},{"id":"W2608835133","doi":"10.1038/ng.3849","title":"Genomic consequences of aberrant DNA repair mechanisms stratify ovarian cancer histotypes","year":2017,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Ovarian cancer diagnosis and treatment","field":"Medicine","cited_by":290,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Vancouver General Hospital; Canada's Michael Smith Genome Sciences Centre; Université de Montréal; Child and Family Research Institute; Centre Hospitalier de l’Université de Montréal; University of British Columbia; BC Cancer Agency","funders":"BC Cancer Agency; Jikei University School of Medicine; University of British Columbia","keywords":"Biology; Microsatellite instability; Ovarian cancer; Cell of origin; Point mutation; DNA mismatch repair; Genome instability; Serous fluid; Genetics; Cancer research; Mutation; Cancer; Germline mutation; DNA repair; DNA damage; Microsatellite; Gene; DNA; Allele","score_opus":0.022051652814411453,"score_gpt":0.3069829118030615,"score_spread":0.28493125898865,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2608835133","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9960828,0.0010079044,0.00064466946,0.00022996594,0.000017571292,0.000010999588,0.0004085132,0.000025327212,0.0015722635],"genre_scores_gemma":[0.9988663,0.00026269452,0.00020861224,0.000062840605,0.00001471387,0.0000035576477,0.00024758177,0.000014201806,0.00031952257],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99973303,0.00005615089,0.000018636145,0.000060696104,0.00005644328,0.00007498193],"domain_scores_gemma":[0.99931335,0.00020387386,0.00026525022,0.00009515818,0.000043064116,0.00007932828],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00032443122,0.00021159303,0.0003138342,0.0012163202,0.00021693297,0.00064873113,0.0002572359,0.00047593392,0.0030687703],"category_scores_gemma":[0.0012100724,0.00018801582,0.0003013949,0.000516958,0.00030385627,0.00028273134,0.0004835365,0.00041936396,0.00039105004],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0011969826,0.00004668869,0.89737284,0.00003975692,0.0002639246,0.0007504715,0.00016083337,0.0007383787,0.07458368,0.0010940038,0.00055803073,0.023194522],"study_design_scores_gemma":[0.00002400322,0.00012947254,0.98582864,0.000015874892,0.00016981101,0.0021310493,0.00019747364,0.00077268097,0.0068281232,0.0021003697,0.0017891594,0.000013476212],"about_ca_topic_score_codex":0.00058158865,"about_ca_topic_score_gemma":0.0010754501,"teacher_disagreement_score":0.0030687703,"about_ca_system_score_codex":0.00022569334,"about_ca_system_score_gemma":0.00013847165,"threshold_uncertainty_score":0.010266066},"labels":[],"label_agreement":null},{"id":"W2608920382","doi":"10.1038/ng.3841","title":"Genomic analyses identify hundreds of variants associated with age at menarche and support a role for puberty timing in cancer risk","year":2017,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Ovarian cancer diagnosis and treatment","field":"Medicine","cited_by":646,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University Health Network; University of Toronto; Lunenfeld-Tanenbaum Research Institute; Mount Sinai Hospital","funders":"Eunice Kennedy Shriver National Institute of Child Health and Human Development; National Heart, Lung, and Blood Institute; National Institute on Aging; Medical Research Council; National Institute for Health and Care Research; Wellcome Trust; Francis Crick Institute; British Heart Foundation; National Cancer Institute; National Institutes of Health; Cancer Research UK","keywords":"Biology; Menarche; Genetics; Cancer; Bioinformatics; Oncology; Computational biology; Endocrinology","score_opus":0.05620437079251206,"score_gpt":0.3844773673354305,"score_spread":0.3282729965429184,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2608920382","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9543979,0.015994819,0.010131157,0.0028261696,0.00065743626,0.000038344206,0.01132415,0.0002910556,0.0043389946],"genre_scores_gemma":[0.98847103,0.0027436258,0.0039011633,0.0005544684,0.00027326046,0.000023035156,0.00261627,0.000113345275,0.0013038132],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99925214,0.0001296812,0.000072499184,0.00033251426,0.00013551944,0.00007751812],"domain_scores_gemma":[0.9969913,0.0018710162,0.0006809001,0.00018366436,0.00008886258,0.0001842382],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00066365715,0.00092217576,0.00058536,0.0015633255,0.000650327,0.0011911159,0.0006937661,0.0010478381,0.0059796837],"category_scores_gemma":[0.0030996334,0.0003772826,0.0016930915,0.0025441162,0.0006085061,0.00039570057,0.0006151209,0.0012408881,0.0004625176],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0015927736,0.00010373378,0.88732797,0.00051832234,0.005604935,0.0055817096,0.0004994731,0.0019985097,0.042413387,0.0031630925,0.0039941026,0.04720198],"study_design_scores_gemma":[0.00014762429,0.00012685453,0.96894383,0.00017673489,0.0033830826,0.0040754173,0.00025228062,0.0020787602,0.004949234,0.0043678796,0.011437179,0.00006116205],"about_ca_topic_score_codex":0.0049352637,"about_ca_topic_score_gemma":0.006549772,"teacher_disagreement_score":0.0059796837,"about_ca_system_score_codex":0.00024965158,"about_ca_system_score_gemma":0.00037444258,"threshold_uncertainty_score":0.020004034},"labels":[],"label_agreement":null},{"id":"W2609142666","doi":"10.1038/ng0205-111","title":"Assessing the validity of the association between the SUMO4 M55V variant and risk of type 1 diabetes","year":2005,"lang":"en","type":"letter","venue":"Nature Genetics","topic":"Diabetes and associated disorders","field":"Biochemistry, Genetics and Molecular Biology","cited_by":44,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Toronto; St. John’s Health Sciences Centre; McGill University and Génome Québec Innovation Centre; Public Health Ontario; Hospital for Sick Children; Memorial University of Newfoundland; McGill University; Montreal Children's Hospital","funders":"","keywords":"Biology; Type 2 diabetes; Association (psychology); Genetics; Genome-wide association study; Genetic association; Diabetes mellitus; Single-nucleotide polymorphism; Gene; Endocrinology; Genotype; Psychology","score_opus":0.00809914797587183,"score_gpt":0.24866327315068876,"score_spread":0.24056412517481693,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2609142666","genre_codex":"commentary","genre_gemma":"commentary","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"commentary","genre_consensus":"commentary","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.28018433,0.0038631177,0.0017500811,0.6844534,0.015864031,0.000069378795,0.00054952723,0.000057875244,0.013208308],"genre_scores_gemma":[0.7777753,0.0017780417,0.0018978504,0.19210686,0.023160685,0.000056769954,0.00022966917,0.000037212365,0.002957578],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99330586,0.003753152,0.000994567,0.0005375029,0.0010105055,0.0003983814],"domain_scores_gemma":[0.9364074,0.05222315,0.0014347403,0.002172515,0.006422074,0.0013400654],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.008948601,0.00049506786,0.0013519877,0.00074542745,0.0012990648,0.0014273159,0.0015828694,0.011823691,0.00244733],"category_scores_gemma":[0.08179385,0.00031754147,0.00086291565,0.0005738947,0.0017385879,0.001159163,0.00088657625,0.0073358263,0.0015134261],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0052350718,0.00053782796,0.5662663,0.00041011622,0.0011128983,0.07454197,0.0030341886,0.0011934476,0.007498225,0.0069124135,0.22723627,0.10602132],"study_design_scores_gemma":[0.0028308164,0.0036695444,0.47229686,0.0016196936,0.0017644301,0.17699212,0.0073594563,0.023743944,0.012875639,0.06774488,0.22856475,0.0005377981],"about_ca_topic_score_codex":0.0027079182,"about_ca_topic_score_gemma":0.0019969398,"teacher_disagreement_score":0.011823691,"about_ca_system_score_codex":0.0010919247,"about_ca_system_score_gemma":0.00070984557,"threshold_uncertainty_score":0.047325253},"labels":[],"label_agreement":null},{"id":"W2612427157","doi":"10.1038/ng.3892","title":"Large-scale association analysis identifies new lung cancer susceptibility loci and heterogeneity in genetic susceptibility across histological subtypes","year":2017,"lang":"en","type":"review","venue":"Nature Genetics","topic":"Genetic Associations and Epidemiology","field":"Biochemistry, Genetics and Molecular Biology","cited_by":794,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Université Laval; St. Paul's Hospital; Centre for Addiction and Mental Health; Institut universitaire de cardiologie et de pneumologie de Québec; University of British Columbia; Public Health Ontario; University of Toronto; University Health Network; Sinai Health System; Lunenfeld-Tanenbaum Research Institute; Princess Margaret Cancer Centre; BC Cancer Agency","funders":"National Cancer Institute; Medical Research Council; Université Laval; Fonds de Recherche du Québec - Santé; Canadian Institutes of Health Research; Novo Nordisk Fonden; Cancer Research UK; Wellcome Trust; Cancer Care Ontario; Institut universitaire de cardiologie et de pneumologie de Québec, Université Laval; National Institute on Drug Abuse; Dartmouth College; World Health Organization","keywords":"Biology; Lung cancer; Genetics; Lung cancer susceptibility; Genome-wide association study; Genetic association; Computational biology; Single-nucleotide polymorphism; Genotype; Gene; Pathology","score_opus":0.029420303371524768,"score_gpt":0.385050658309201,"score_spread":0.3556303549376762,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2612427157","genre_codex":"review","genre_gemma":"review","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"review","genre_consensus":"review","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.00019123108,0.9972543,0.00041933527,0.0012211647,0.00031400964,0.0000045546262,0.000079769976,0.000012352406,0.00050334586],"genre_scores_gemma":[0.0012460832,0.9961701,0.00052714173,0.000982258,0.0005354275,0.000009288782,0.00013011401,0.0000037926504,0.0003959049],"study_design_codex":"design_other","study_design_gemma":"observational","domain_scores_codex":[0.99949217,0.000103447164,0.00007401889,0.00013179096,0.00015821554,0.00004040574],"domain_scores_gemma":[0.99755836,0.0015998184,0.00022491577,0.0000746292,0.000402144,0.00014014849],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0024219032,0.00096741493,0.002141772,0.0017425972,0.00023690255,0.0014483657,0.0015288834,0.001680689,0.0025575843],"category_scores_gemma":[0.0031580671,0.0003488912,0.00081225444,0.0022333008,0.0008162825,0.00119008,0.0011197628,0.0024544788,0.0011650482],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00019503041,0.000045782137,0.0029459966,0.010896405,0.00058482046,0.0003509798,0.00006095881,0.00033515584,0.0011902063,0.0046151425,0.047540084,0.9312395],"study_design_scores_gemma":[0.00008985702,0.00009348937,0.010098687,0.007709443,0.0012271502,0.0022542737,0.00014931399,0.00020672427,0.0005655002,0.010444558,0.9670843,0.00007672784],"about_ca_topic_score_codex":0.0018563115,"about_ca_topic_score_gemma":0.0038785436,"teacher_disagreement_score":0.0025575843,"about_ca_system_score_codex":0.00076351274,"about_ca_system_score_gemma":0.0021316267,"threshold_uncertainty_score":0.0128083825},"labels":[],"label_agreement":null},{"id":"W2613118383","doi":"10.1038/ng.3861","title":"Recurrent noncoding regulatory mutations in pancreatic ductal adenocarcinoma","year":2017,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Pancreatic and Hepatic Oncology Research","field":"Medicine","cited_by":70,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Toronto General Hospital; Lunenfeld-Tanenbaum Research Institute; Mount Sinai Hospital; Ontario Institute for Cancer Research; University of Toronto","funders":"National Human Genome Research Institute; National Institute of General Medical Sciences; Medical Research Council; National Cancer Institute; Cancer Research UK; Wellcome Trust; Pancreatic Cancer UK","keywords":"Biology; Genetics; Gene; Carcinogenesis; Regulatory sequence; Homeobox; Somatic cell; Mutation; Regulation of gene expression; Cancer research; Transcription factor","score_opus":0.03649920250970608,"score_gpt":0.36898510899098846,"score_spread":0.3324859064812824,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2613118383","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99587965,0.0010550084,0.00088309584,0.00017067535,0.00004694503,0.000008925026,0.00032385768,0.000089563655,0.001542299],"genre_scores_gemma":[0.9988079,0.00022215294,0.00043472726,0.000059553833,0.000028192339,0.0000027908234,0.00013020672,0.000023622844,0.00029071077],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9995716,0.000050937073,0.00007412488,0.000084851294,0.00015390292,0.000064459426],"domain_scores_gemma":[0.9992213,0.00026763658,0.0002198667,0.00008932461,0.000071636074,0.00013021952],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00031537795,0.0002454418,0.0003691099,0.001181026,0.00043921534,0.0006237276,0.00033962316,0.0007509542,0.0016754725],"category_scores_gemma":[0.0015863321,0.00017198251,0.00036856576,0.0009407909,0.00036991958,0.00021996743,0.00034225202,0.00044173966,0.000504465],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0015097931,0.00021810934,0.39262906,0.00023320975,0.00033494068,0.07004273,0.001077674,0.0025047471,0.440235,0.0024096246,0.0020627817,0.086742334],"study_design_scores_gemma":[0.00015939288,0.0006818443,0.66243905,0.00012721028,0.0009266487,0.19510682,0.0010374945,0.007791795,0.11015866,0.0041454746,0.017311739,0.000113863534],"about_ca_topic_score_codex":0.0011987551,"about_ca_topic_score_gemma":0.0019872861,"teacher_disagreement_score":0.0016754725,"about_ca_system_score_codex":0.0003533195,"about_ca_system_score_gemma":0.000265901,"threshold_uncertainty_score":0.005605042},"labels":[],"label_agreement":null},{"id":"W2617037207","doi":"10.1038/ng.3875","title":"Genetic association study of exfoliation syndrome identifies a protective rare variant at LOXL1 and five new susceptibility loci","year":2017,"lang":"en","type":"review","venue":"Nature Genetics","topic":"Microbial metabolism and enzyme function","field":"Biochemistry, Genetics and Molecular Biology","cited_by":158,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Dalhousie University","funders":"National Eye Institute; National Cancer Institute; National Heart, Lung, and Blood Institute","keywords":"Biology; Genetics; Genetic association; Genetic predisposition; Genome-wide association study; Genotype; Single-nucleotide polymorphism; Gene","score_opus":0.020225296359029497,"score_gpt":0.2993521405903621,"score_spread":0.2791268442313326,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2617037207","genre_codex":"review","genre_gemma":"review","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"review","genre_consensus":"review","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.00022964265,0.99792445,0.00035828818,0.0005846731,0.00028643067,0.0000032408068,0.000033776007,0.000010650322,0.0005688911],"genre_scores_gemma":[0.0016194541,0.9958001,0.0005835703,0.00060015544,0.00054331194,0.000007873478,0.00009586949,0.0000032243368,0.00074652483],"study_design_codex":"design_other","study_design_gemma":"observational","domain_scores_codex":[0.99975497,0.00003653045,0.000047140744,0.00005184513,0.00008613568,0.000023307713],"domain_scores_gemma":[0.99944586,0.00030097406,0.00008142439,0.000015104981,0.00010363651,0.000053002866],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0008888342,0.0009258775,0.00145727,0.0014985544,0.00017146001,0.0008625162,0.0011712026,0.0012964668,0.0018104005],"category_scores_gemma":[0.0010306706,0.00021898767,0.00038592634,0.0012228091,0.0005145457,0.0008049683,0.0006889589,0.0018380282,0.0009284525],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00018405919,0.000044807162,0.0010631252,0.008988116,0.00019227693,0.0010898259,0.000040276962,0.00023163627,0.0025616188,0.003380226,0.030511964,0.9517121],"study_design_scores_gemma":[0.000069846305,0.00007577717,0.0027934005,0.0029494148,0.0004088775,0.00510339,0.00007195667,0.00010925513,0.0011268021,0.003060503,0.9841956,0.000035331595],"about_ca_topic_score_codex":0.00076231454,"about_ca_topic_score_gemma":0.0014207,"teacher_disagreement_score":0.0018104005,"about_ca_system_score_codex":0.00051333517,"about_ca_system_score_gemma":0.0009674509,"threshold_uncertainty_score":0.0060563684},"labels":[],"label_agreement":null},{"id":"W2619003201","doi":"10.1038/s41588-018-0084-1","title":"Refining the accuracy of validated target identification through coding variant fine-mapping in type 2 diabetes","year":2018,"lang":"en","type":"review","venue":"Nature Genetics","topic":"AI in cancer detection","field":"Computer Science","cited_by":470,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"McGill University; McGill University and Génome Québec Innovation Centre; Université de Sherbrooke","funders":"National Institute of General Medical Sciences; National Heart, Lung, and Blood Institute; NIHR Cambridge Biomedical Research Centre; Helmholtz Zentrum München; Korea Centers for Disease Control and Prevention; Korea National Institute of Health; National Center for Advancing Translational Sciences; Medical Research Council; Münchner Zentrum für Gesundheitswissenschaften; Erasmus Medisch Centrum; Genentech; Nederlandse Organisatie voor Wetenschappelijk Onderzoek; Centers for Disease Control and Prevention; Regeneron Pharmaceuticals; National Institutes of Health; Hjartavernd; Novo Nordisk Fonden; Eli Lilly and Company; Lundbeckfonden; ZonMw; British Heart Foundation; European Commission; Steno Diabetes Center Copenhagen; Wellcome Trust; Bundesministerium für Bildung und Forschung; National Institute on Aging; National Institute for Health and Care Research; National Institute of Diabetes and Digestive and Kidney Diseases; Sanofi; GlaxoSmithKline; Pfizer; Incyte; Yale University","keywords":"Biology; Computational biology; Identification (biology); Coding (social sciences); Refining (metallurgy); Type 2 diabetes; Genetics; Diabetes mellitus; Statistics; Endocrinology; Mathematics","score_opus":0.05926589266483752,"score_gpt":0.34457261975839104,"score_spread":0.28530672709355354,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2619003201","genre_codex":"review","genre_gemma":"review","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"review","genre_consensus":"review","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.00140476,0.99301744,0.0032970535,0.0008556993,0.00023813432,0.0000083973455,0.00012887736,0.000039281018,0.0010104742],"genre_scores_gemma":[0.02996184,0.96124583,0.0049599297,0.001795637,0.0005933986,0.000026689313,0.0004222068,0.00002836236,0.00096609537],"study_design_codex":"design_other","study_design_gemma":"simulation_or_modeling","domain_scores_codex":[0.9987379,0.0003810785,0.00012793679,0.00030928137,0.00036585648,0.00007796922],"domain_scores_gemma":[0.9939468,0.004946743,0.00030598193,0.0001522216,0.0005848867,0.00006339395],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0038023947,0.00087038276,0.0022295679,0.0018585382,0.00016999425,0.0015312735,0.0020132498,0.001637889,0.0017947492],"category_scores_gemma":[0.008438307,0.00036423033,0.0011746051,0.001593683,0.0007879505,0.0009180895,0.00077221356,0.0019722749,0.00093727844],"study_design_candidate":"simulation_or_modeling","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00018766083,0.000038623173,0.003396772,0.00494279,0.00045886822,0.00017260942,0.000036497793,0.0008574137,0.0013475394,0.0036753037,0.0070077204,0.9778782],"study_design_scores_gemma":[0.0002374842,0.0006708839,0.03193295,0.01632956,0.0055496315,0.009007976,0.00027817988,0.010025977,0.01548077,0.049788512,0.860426,0.00027209372],"about_ca_topic_score_codex":0.0017825223,"about_ca_topic_score_gemma":0.0021838145,"teacher_disagreement_score":0.0038023947,"about_ca_system_score_codex":0.00072852545,"about_ca_system_score_gemma":0.0010745571,"threshold_uncertainty_score":0.020109177},"labels":[],"label_agreement":null},{"id":"W2619767973","doi":"10.1038/ng.3874","title":"Fifteen new risk loci for coronary artery disease highlight arterial-wall-specific mechanisms","year":2017,"lang":"en","type":"review","venue":"Nature Genetics","topic":"Genetic Associations and Epidemiology","field":"Biochemistry, Genetics and Molecular Biology","cited_by":322,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"York University","funders":"National Center for Advancing Translational Sciences; National Institute of Diabetes and Digestive and Kidney Diseases; Pfizer; National Heart, Lung, and Blood Institute; Medical Research Council; European Commission; NIHR Cambridge Biomedical Research Centre; British Heart Foundation; National Institute of Environmental Health Sciences; National Institute for Health and Care Research; National Institutes of Health; U.S. Department of Health and Human Services","keywords":"Biology; Coronary artery disease; Arterial disease; Arterial wall; Internal medicine; Genetics; Cardiology; Vascular disease; Medicine","score_opus":0.03592111552459162,"score_gpt":0.323395064665272,"score_spread":0.2874739491406804,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2619767973","genre_codex":"review","genre_gemma":"review","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"review","genre_consensus":"review","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.0005262486,0.99678767,0.0006883454,0.00091258716,0.00034003612,0.0000036724023,0.00005862382,0.000016632877,0.000666231],"genre_scores_gemma":[0.0029407167,0.9943798,0.0007601858,0.0006484157,0.0005621694,0.00000778617,0.00013252422,0.000003837126,0.0005646141],"study_design_codex":"design_other","study_design_gemma":"systematic_review","domain_scores_codex":[0.9997173,0.00004680658,0.000042388452,0.00007085852,0.00008530654,0.00003724081],"domain_scores_gemma":[0.9992416,0.00045417462,0.00009682015,0.000022848651,0.00012852924,0.000056028417],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0011722009,0.000936592,0.0015428769,0.0014787469,0.00019953174,0.001160801,0.0011893967,0.0012811712,0.0021441816],"category_scores_gemma":[0.0015697903,0.00026449066,0.0005857071,0.0014089154,0.0007259045,0.0011075146,0.0010758716,0.0017566035,0.0008848373],"study_design_candidate":"systematic_review","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00022840034,0.00004616531,0.0029909788,0.008279444,0.00041232386,0.00063154084,0.00008874248,0.00040427496,0.003187069,0.007885686,0.023954203,0.9518911],"study_design_scores_gemma":[0.00008759873,0.000154031,0.009217848,0.0057045934,0.001195379,0.0036543603,0.00017828657,0.0002548081,0.0019268874,0.015605414,0.96194005,0.00008069535],"about_ca_topic_score_codex":0.0008222551,"about_ca_topic_score_gemma":0.0015954829,"teacher_disagreement_score":0.0021441816,"about_ca_system_score_codex":0.00056597387,"about_ca_system_score_gemma":0.0012158656,"threshold_uncertainty_score":0.0071730018},"labels":[],"label_agreement":null},{"id":"W2705861159","doi":"10.1038/ng.3901","title":"Disease model discovery from 3,328 gene knockouts by The International Mouse Phenotyping Consortium","year":2017,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Genetics and Physical Performance","field":"Biochemistry, Genetics and Molecular Biology","cited_by":268,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Hospital for Sick Children; Toronto Centre for Phenogenomics","funders":"National Cancer Institute; National Human Genome Research Institute; National Institutes of Health; Agence Nationale de la Recherche; Wellcome Trust","keywords":"Biology; Phenome; Computational biology; Genetics; Gene; Phenotype; Genome; OMIM : Online Mendelian Inheritance in Man; Gene knockout; Human genome; Disease; Medicine","score_opus":0.008547893132521422,"score_gpt":0.2539222884389956,"score_spread":0.2453743953064742,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2705861159","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.61691886,0.0124458475,0.23326793,0.004275409,0.0005114075,0.00047285197,0.11257199,0.0067814095,0.012754226],"genre_scores_gemma":[0.525886,0.008881526,0.24538419,0.0011609888,0.0001900019,0.0005797376,0.2097297,0.0018438312,0.0063440483],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.99882764,0.00027170344,0.000100802936,0.00024838906,0.00045899418,0.000092371774],"domain_scores_gemma":[0.9979007,0.00074084406,0.00025056087,0.00052589097,0.00036703024,0.00021507363],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0040132846,0.0009822606,0.0011454517,0.0030479827,0.00048512948,0.0010894845,0.00084320374,0.0006047492,0.00245309],"category_scores_gemma":[0.0035357636,0.0005797131,0.0015923816,0.0013677465,0.00022974361,0.00042966573,0.0010697468,0.0011065502,0.00074163376],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0027231602,0.00040155507,0.07196962,0.001028687,0.002012664,0.0017650892,0.00021046582,0.02127744,0.53119165,0.00836775,0.062239118,0.29681286],"study_design_scores_gemma":[0.0016757943,0.0014090247,0.27044427,0.00093288143,0.0059471205,0.0052440264,0.00029178205,0.13137515,0.25910345,0.03498897,0.28817612,0.00041139938],"about_ca_topic_score_codex":0.0025408259,"about_ca_topic_score_gemma":0.0063458844,"teacher_disagreement_score":0.0040132846,"about_ca_system_score_codex":0.00070007,"about_ca_system_score_gemma":0.0016254327,"threshold_uncertainty_score":0.021224558},"labels":[],"label_agreement":null},{"id":"W2724118546","doi":"10.1038/ng.3902","title":"Epigenetic modifier drugs trigger widespread transcription of endogenous retroviruses","year":2017,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Genomics and Chromatin Dynamics","field":"Biochemistry, Genetics and Molecular Biology","cited_by":7,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of British Columbia; BC Cancer Agency","funders":"","keywords":"Biology; Endogenous retrovirus; Epigenetics; Epigenome; Transcription (linguistics); Genetics; Endogeny; Transcription factor; Gene; Computational biology; Genome; DNA methylation; Gene expression","score_opus":0.014548067360491116,"score_gpt":0.2524512162280808,"score_spread":0.2379031488675897,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2724118546","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.98566633,0.0026928014,0.0059315213,0.00021738604,0.00012260977,0.000071936556,0.00049307896,0.00035713904,0.0044473363],"genre_scores_gemma":[0.9965467,0.00035444152,0.0010768127,0.0000803385,0.000019371108,0.000021001406,0.00019820848,0.00004523137,0.0016579214],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9994941,0.00007421618,0.000028171326,0.00012402289,0.00012843209,0.00015114751],"domain_scores_gemma":[0.99961686,0.00016579387,0.00006926724,0.00007148082,0.000022191693,0.000054403492],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00030465395,0.00031785102,0.00047118627,0.00037777008,0.00016879561,0.0007416225,0.00029190446,0.0005052884,0.0030150267],"category_scores_gemma":[0.0004264517,0.00027539305,0.0003881856,0.00018981313,0.0004034517,0.0003122825,0.00040964046,0.0011066641,0.0005820179],"study_design_candidate":"bench_or_experimental","study_design_consensus":"bench_or_experimental","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00015974324,0.00004936986,0.00016890587,0.000016198122,0.0000065500158,0.00004538801,0.000008418797,0.000100451776,0.99702114,0.0003541878,0.00006357791,0.0020060632],"study_design_scores_gemma":[0.000028519857,0.00033607648,0.002114877,0.0000038485473,0.000012130063,0.00011240047,0.000020333957,0.0009509403,0.9954847,0.00017070546,0.00076173776,0.0000037874504],"about_ca_topic_score_codex":0.00033887636,"about_ca_topic_score_gemma":0.00081597414,"teacher_disagreement_score":0.0030150267,"about_ca_system_score_codex":0.00056929793,"about_ca_system_score_gemma":0.00018847962,"threshold_uncertainty_score":0.010086298},"labels":[],"label_agreement":null},{"id":"W2725027816","doi":"10.1038/ng.3908","title":"Transposase-driven rearrangements in human tumors","year":2017,"lang":"en","type":"article","venue":"Nature Genetics","topic":"RNA modifications and cancer","field":"Biochemistry, Genetics and Molecular Biology","cited_by":2,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Hospital for Sick Children","funders":"","keywords":"Transposase; Biology; Gene; Identification (biology); Genetics; Suppressor; Computational biology; Tumor suppressor gene; DNA; Cancer research; Transposable element; Carcinogenesis; Genome","score_opus":0.013137215535551411,"score_gpt":0.30484817098603423,"score_spread":0.2917109554504828,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2725027816","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9913625,0.0019937526,0.001757437,0.00028041343,0.00002122808,0.000018105171,0.0002990858,0.00009362499,0.0041737533],"genre_scores_gemma":[0.99672866,0.0005740819,0.00027866184,0.00004028061,0.000006924152,0.000004446935,0.00015538694,0.000012005625,0.0021995448],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9999291,0.000011832978,0.000004740114,0.000016255379,0.000019767283,0.000018333183],"domain_scores_gemma":[0.99993706,0.000017705128,0.000015988846,0.000009154377,0.0000043176533,0.000015838326],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.000096243086,0.00012312237,0.000103887105,0.00043069094,0.000120623765,0.00027929002,0.000116321164,0.00033616254,0.0030078143],"category_scores_gemma":[0.0001939513,0.00015128365,0.00011453601,0.00025638234,0.00018075506,0.00011598856,0.00015165079,0.00024366993,0.00033802792],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00038408104,0.000034439978,0.0064673615,0.000044432418,0.000029053914,0.0017179099,0.000109563654,0.00047701705,0.9749834,0.0033285504,0.00037329792,0.012050803],"study_design_scores_gemma":[0.0001152006,0.0007166317,0.15737148,0.000037051504,0.00017314716,0.030953249,0.00038737012,0.002976637,0.7784813,0.005298207,0.023461908,0.000027859569],"about_ca_topic_score_codex":0.0008943536,"about_ca_topic_score_gemma":0.0013314614,"teacher_disagreement_score":0.0030078143,"about_ca_system_score_codex":0.00025478503,"about_ca_system_score_gemma":0.00013930413,"threshold_uncertainty_score":0.0100620985},"labels":[],"label_agreement":null},{"id":"W2730344022","doi":"10.1038/ng.3911","title":"Ancient selection for derived alleles at a GDF5 enhancer influencing human growth and osteoarthritis risk","year":2017,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Genetics and Physical Performance","field":"Biochemistry, Genetics and Molecular Biology","cited_by":109,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Waterloo","funders":"National Institute of Arthritis and Musculoskeletal and Skin Diseases","keywords":"Enhancer; Biology; Allele; Genetics; Locus (genetics); Phenotype; Haplotype; Gene; Evolutionary biology; Gene expression","score_opus":0.005643424439315035,"score_gpt":0.2574544383472391,"score_spread":0.25181101390792404,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2730344022","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9972567,0.0001831982,0.0014115492,0.000074984964,0.000013940339,0.000008558273,0.00011863445,0.000022999895,0.0009095377],"genre_scores_gemma":[0.99803215,0.0000958117,0.00086830714,0.000070898066,0.000012430894,0.000003932391,0.00011188839,0.000022597365,0.00078207586],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.99964523,0.00008085211,0.000027317152,0.00010117411,0.000084924905,0.000060485534],"domain_scores_gemma":[0.99966836,0.00011104813,0.00005065318,0.000055989305,0.000026506183,0.00008749331],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00046636214,0.0003743837,0.00036256656,0.00073456374,0.00032395712,0.00031039264,0.0006070868,0.000491233,0.003925996],"category_scores_gemma":[0.00060634204,0.0002577979,0.00032864162,0.00043803785,0.0005799513,0.00014984384,0.000672095,0.0006936415,0.00022462787],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0012958335,0.00016844657,0.059109136,0.00008588587,0.00029194247,0.0030358012,0.0003077456,0.0006880722,0.9120612,0.0035785304,0.00017887472,0.019198604],"study_design_scores_gemma":[0.00044188998,0.00084922765,0.8649626,0.00009777157,0.000724297,0.016088493,0.00050435035,0.004932063,0.10248049,0.003349542,0.0054632677,0.00010603412],"about_ca_topic_score_codex":0.0008512338,"about_ca_topic_score_gemma":0.0017629066,"teacher_disagreement_score":0.003925996,"about_ca_system_score_codex":0.00026030728,"about_ca_system_score_gemma":0.00023047376,"threshold_uncertainty_score":0.013133824},"labels":[],"label_agreement":null},{"id":"W2735404270","doi":"10.1038/ng.3913","title":"Association analyses based on false discovery rate implicate new loci for coronary artery disease","year":2017,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Genetic Associations and Epidemiology","field":"Biochemistry, Genetics and Molecular Biology","cited_by":794,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Canadian Heart Research Centre; University of Ottawa","funders":"NIHR Sheffield Biomedical Research Centre; European Regional Development Fund; Interreg; Pirkanmaan Rahasto; National Institutes of Health; Tays; Novo Nordisk Fonden; Diabetesliitto; Tampereen Tuberkuloosisäätiö; Medical Research Council; Signe ja Ane Gyllenbergin Säätiö; Stockholms Läns Landsting; Knut och Alice Wallenbergs Stiftelse; Suomen Kulttuurirahasto; Karolinska Institutet; Novo Nordisk; Hjärt-Lungfonden; British Heart Foundation; National Institute for Health and Care Research; Imperial College Healthcare NHS Trust; Wellcome Trust; Canadian Institutes of Health Research; Yrjö Jahnssonin Säätiö; Pfizer; Biogen; European Commission; Sanofi; Torsten Söderbergs Stiftelse; Vetenskapsrådet; Emil Aaltosen Säätiö; AstraZeneca; Eli Lilly and Company; Sihtasutus Archimedes; Imperial College London; Andrea and Charles Bronfman Philanthropies","keywords":"Genome-wide association study; False discovery rate; Biology; Coronary artery disease; Genetic association; Genetics; Biobank; Multiple comparisons problem; Bioinformatics; Computational biology; Single-nucleotide polymorphism; Internal medicine; Medicine; Gene; Genotype","score_opus":0.025239962041642888,"score_gpt":0.33620035641005835,"score_spread":0.3109603943684155,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2735404270","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.59915954,0.009401958,0.3730449,0.007272956,0.0023607316,0.00021432612,0.0011551898,0.0015437339,0.0058466764],"genre_scores_gemma":[0.9735588,0.0005899078,0.022787347,0.0011421596,0.0006346886,0.000077735014,0.00024252389,0.00021001349,0.00075686374],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.923309,0.046298973,0.005616065,0.010324886,0.012348394,0.0021025739],"domain_scores_gemma":[0.50064945,0.43505117,0.02342808,0.032971356,0.005519267,0.0023807008],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.11630137,0.0017019997,0.002217398,0.0046277936,0.0015670529,0.0042421976,0.004229667,0.0036118065,0.0025414266],"category_scores_gemma":[0.20209992,0.0012514776,0.0037218109,0.0032018425,0.005025867,0.0037340594,0.0017901617,0.0068297293,0.0004750157],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0038035868,0.0003277482,0.86537755,0.00065222516,0.01547705,0.0043389075,0.0011152214,0.005790771,0.013984363,0.02386026,0.0027610604,0.06251135],"study_design_scores_gemma":[0.00092640845,0.0016374529,0.7083063,0.00032764557,0.009079289,0.018448852,0.0005802748,0.12044328,0.018039852,0.11670257,0.00520442,0.00030366104],"about_ca_topic_score_codex":0.001101684,"about_ca_topic_score_gemma":0.00097213674,"teacher_disagreement_score":0.11630137,"about_ca_system_score_codex":0.0008887508,"about_ca_system_score_gemma":0.0011812296,"threshold_uncertainty_score":0.61506784},"labels":[],"label_agreement":null},{"id":"W2738082385","doi":"10.1038/s41588-018-0090-3","title":"Genome-wide association analyses identify 44 risk variants and refine the genetic architecture of major depression","year":2018,"lang":"en","type":"review","venue":"Nature Genetics","topic":"Genetic Associations and Epidemiology","field":"Biochemistry, Genetics and Molecular Biology","cited_by":3303,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Dalhousie University; University of Toronto; Centre for Addiction and Mental Health; University of British Columbia","funders":"Cilag; National Institute of Environmental Health Sciences; National Institute of Neurological Disorders and Stroke; National Cancer Institute; Novo Nordisk; National Institute on Drug Abuse; Wellcome Trust; NODAI Genome Research Center, Tokyo University of Agriculture; Medical Research Council; National Institutes of Health; National Institute of General Medical Sciences; H. Lundbeck A/S; Westfälische Wilhelms-Universität Münster; Bundesministerium für Bildung und Forschung; National Institute for Health and Care Research; Amgen; Siemens Healthineers; Max-Planck-Gesellschaft; Lundbeckfonden; National Institute of Mental Health; National Heart, Lung, and Blood Institute; Northwestern University; Pfizer; National Human Genome Research Institute; Erasmus Medisch Centrum; GlaxoSmithKline","keywords":"Biology; Genome-wide association study; Genetic architecture; Genetic association; Computational biology; Association (psychology); Genetics; Evolutionary biology; Single-nucleotide polymorphism; Quantitative trait locus; Genotype; Gene; Psychology","score_opus":0.020965185641811004,"score_gpt":0.34642732301541007,"score_spread":0.3254621373735991,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2738082385","genre_codex":"review","genre_gemma":"review","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"review","genre_consensus":"review","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.0003056394,0.9969014,0.00046197244,0.0014991408,0.00025627422,0.0000037789039,0.00007321947,0.0000120281975,0.0004865677],"genre_scores_gemma":[0.002310471,0.99547845,0.0005256887,0.0008371363,0.00040724382,0.0000063612097,0.00010869833,0.0000032877813,0.00032265493],"study_design_codex":"design_other","study_design_gemma":"meta_analysis","domain_scores_codex":[0.9996543,0.00006391955,0.000054390643,0.00009415084,0.00010199073,0.00003132162],"domain_scores_gemma":[0.9986513,0.0008704432,0.00014331234,0.00004207364,0.00022444593,0.000068475645],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0015030254,0.0009463378,0.0015178077,0.0015960125,0.00020882396,0.0010760188,0.0013012845,0.0014283301,0.0018978211],"category_scores_gemma":[0.0024853246,0.00028664985,0.0007569885,0.0018716092,0.000740909,0.00089043373,0.00087259116,0.0021006514,0.00076129567],"study_design_candidate":"meta_analysis","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00017513124,0.000040321574,0.0030576962,0.007016057,0.00057404325,0.0003560694,0.00005672161,0.00033455476,0.0010958555,0.0054650623,0.026071744,0.9557567],"study_design_scores_gemma":[0.00012416599,0.00013818585,0.019977542,0.00928453,0.002123118,0.0035680467,0.00018474125,0.00032994035,0.00088492315,0.020136697,0.94315326,0.00009475219],"about_ca_topic_score_codex":0.0022762073,"about_ca_topic_score_gemma":0.0040181517,"teacher_disagreement_score":0.0022762073,"about_ca_system_score_codex":0.0006734157,"about_ca_system_score_gemma":0.0016336433,"threshold_uncertainty_score":0.007948816},"labels":[],"label_agreement":null},{"id":"W2739744262","doi":"10.1038/ng.3924","title":"The osteoarthritis and height GDF5 locus yields its secrets","year":2017,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Growth Hormone and Insulin-like Growth Factors","field":"Medicine","cited_by":7,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Montreal Heart Institute; Université de Montréal","funders":"","keywords":"Biology; Locus (genetics); Osteoarthritis; Genetics; Evolutionary biology; Gene; Pathology; Medicine","score_opus":0.011485829748829755,"score_gpt":0.2643857353207306,"score_spread":0.25289990557190084,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2739744262","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9853397,0.0014666115,0.0065925713,0.00085629296,0.00025423497,0.000013286146,0.0013323114,0.0001806374,0.003964278],"genre_scores_gemma":[0.9931577,0.00020708992,0.0014957516,0.00023201355,0.000032811506,0.000005539805,0.0005988169,0.00008593906,0.0041842093],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9996276,0.000038547816,0.0000320006,0.00007823048,0.00014339294,0.00008023038],"domain_scores_gemma":[0.99949265,0.00010449408,0.00013743009,0.000059078528,0.000033735716,0.00017264445],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0002491869,0.0005073519,0.00023604083,0.0006197229,0.0002628704,0.00059079455,0.0004433448,0.0006853402,0.0040224628],"category_scores_gemma":[0.00052769564,0.0003147997,0.00041676994,0.00021002903,0.0005411018,0.00019265301,0.00059093087,0.0009793395,0.0004965173],"study_design_candidate":"bench_or_experimental","study_design_consensus":"bench_or_experimental","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0002314151,0.000014633545,0.00218727,0.000029888208,0.000023990144,0.0006913848,0.00002511325,0.00009731542,0.9919592,0.0011782945,0.00020788399,0.0033536297],"study_design_scores_gemma":[0.00017877728,0.000231844,0.085469745,0.000048579717,0.0001342559,0.0052948473,0.00021702929,0.0022350424,0.891448,0.0018497787,0.012844479,0.000047662914],"about_ca_topic_score_codex":0.0019787175,"about_ca_topic_score_gemma":0.0032596006,"teacher_disagreement_score":0.0040224628,"about_ca_system_score_codex":0.00044679915,"about_ca_system_score_gemma":0.00038702722,"threshold_uncertainty_score":0.013456404},"labels":[],"label_agreement":null},{"id":"W2739793190","doi":"10.1038/ng.3925","title":"Monogenic immune disorders and severe atopic disease","year":2017,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Immunodeficiency and Autoimmune Disorders","field":"Immunology and Microbiology","cited_by":10,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"BC Children's Hospital; University of British Columbia","funders":"","keywords":"Atopy; Atopic dermatitis; Disease; Immune dysregulation; Immune system; Immunology; Biology; Allergy; Medicine; Pathology","score_opus":0.004754462508330309,"score_gpt":0.23169652666142648,"score_spread":0.22694206415309617,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2739793190","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9630215,0.017598346,0.00079325784,0.0019357149,0.00019291538,0.00001122489,0.0001791169,0.00005185745,0.016216112],"genre_scores_gemma":[0.99539965,0.0020510312,0.00026595243,0.00018728962,0.00028368164,0.0000040180644,0.00008538683,0.000008138804,0.0017147142],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9996979,0.00011072338,0.000026858812,0.000043893524,0.000055432454,0.00006519976],"domain_scores_gemma":[0.99949086,0.00013651662,0.00018655197,0.000048375186,0.000026105366,0.00011154654],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00022482651,0.00044968328,0.00026882684,0.00077485584,0.00038643955,0.0005672262,0.0003387798,0.0011962029,0.005927803],"category_scores_gemma":[0.0009158616,0.00019268885,0.00021115932,0.00058246707,0.00059814006,0.000504472,0.00062064885,0.0007812328,0.00042381504],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.005102876,0.0005266621,0.62909406,0.0006054396,0.00059157907,0.15240613,0.00093427894,0.0005231946,0.08344085,0.028315324,0.008552838,0.08990677],"study_design_scores_gemma":[0.00011302316,0.00030009414,0.7397765,0.00018882853,0.00031344438,0.23169275,0.00071219145,0.0006738053,0.0035376768,0.010296728,0.012358054,0.000036882106],"about_ca_topic_score_codex":0.00054073497,"about_ca_topic_score_gemma":0.0007754194,"teacher_disagreement_score":0.005927803,"about_ca_system_score_codex":0.0001821836,"about_ca_system_score_gemma":0.00016408623,"threshold_uncertainty_score":0.019830465},"labels":[],"label_agreement":null},{"id":"W2743661585","doi":"10.1038/ng.3930","title":"TMPRSS2–ERG fusion co-opts master transcription factors and activates NOTCH signaling in primary prostate cancer","year":2017,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Prostate Cancer Treatment and Research","field":"Medicine","cited_by":195,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Toronto General Hospital; Ontario Institute for Cancer Research; University of Toronto; Princess Margaret Cancer Centre; University Health Network","funders":"","keywords":"TMPRSS2; Biology; Notch signaling pathway; Prostate cancer; Transcription factor; Erg; Cancer research; Prostate; Transcription (linguistics); Genetics; Cancer; Computational biology; Signal transduction; Gene; Internal medicine; Neuroscience; Coronavirus disease 2019 (COVID-19); Medicine","score_opus":0.032734845802772736,"score_gpt":0.3369956480270824,"score_spread":0.3042608022243096,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2743661585","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9941288,0.0010914984,0.0005315132,0.00038123675,0.00006323335,0.00002095305,0.00061350164,0.0001369141,0.0030322555],"genre_scores_gemma":[0.99679863,0.0003233294,0.00016935394,0.00007070186,0.000006341945,0.0000088878505,0.00038232823,0.000012405468,0.0022280728],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9995919,0.00004625934,0.000020168933,0.000046752884,0.00012067696,0.00017431675],"domain_scores_gemma":[0.9999075,0.000015813652,0.0000101021915,0.000012753219,0.000009573342,0.00004424571],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0002106648,0.00024028453,0.0003610102,0.00045258264,0.00028286644,0.000616469,0.00024257813,0.00043483626,0.0034583616],"category_scores_gemma":[0.00015689003,0.00025110153,0.00044943154,0.00043184968,0.00038045915,0.00021092266,0.00029598616,0.0008326327,0.0006857445],"study_design_candidate":"bench_or_experimental","study_design_consensus":"bench_or_experimental","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00063120323,0.00022672511,0.0022489766,0.00005667522,0.000028569524,0.0006159904,0.00002943869,0.0003826076,0.9908545,0.00030551504,0.0013551112,0.0032645334],"study_design_scores_gemma":[0.00014144166,0.0012145306,0.059895303,0.000010758996,0.00009517204,0.005892515,0.00033491262,0.0042241123,0.92021894,0.0003380442,0.007614116,0.000020192634],"about_ca_topic_score_codex":0.0035598527,"about_ca_topic_score_gemma":0.006269071,"teacher_disagreement_score":0.0035598527,"about_ca_system_score_codex":0.0009118506,"about_ca_system_score_gemma":0.0005410103,"threshold_uncertainty_score":0.011569321},"labels":[],"label_agreement":null},{"id":"W2746135575","doi":"10.1038/ng.3940","title":"A Children's Oncology Group and TARGET initiative exploring the genetic landscape of Wilms tumor","year":2017,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Renal and related cancers","field":"Biochemistry, Genetics and Molecular Biology","cited_by":370,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of British Columbia; Canada's Michael Smith Genome Sciences Centre","funders":"National Cancer Institute; National Institutes of Health","keywords":"Biology; Wilms' tumor; Germline; Cancer research; Genetics; DNA methylation; Epigenetics; Gene; Gene expression","score_opus":0.009911906717479662,"score_gpt":0.24987214980322078,"score_spread":0.23996024308574113,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2746135575","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.7948565,0.017781023,0.003490296,0.12048306,0.0013389238,0.0005113216,0.018836403,0.0001796485,0.04252288],"genre_scores_gemma":[0.8878001,0.021326035,0.030174218,0.022059167,0.002382066,0.00061467144,0.0121550085,0.00020342146,0.023285262],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9993729,0.000158572,0.000017224214,0.00010076605,0.00015523082,0.00019531419],"domain_scores_gemma":[0.99717546,0.0005914382,0.00023885361,0.00008141766,0.00034751603,0.0015654367],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0021933767,0.0003148135,0.00030197736,0.0013028578,0.0013245038,0.0010470683,0.0009008878,0.0013570957,0.0049127988],"category_scores_gemma":[0.0014142577,0.00017566817,0.00036794663,0.0014671729,0.0005153882,0.00056510494,0.0015132985,0.0017080178,0.00032047514],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0023077575,0.001166842,0.51782876,0.00040120335,0.00046625076,0.0040777544,0.0018020822,0.001609158,0.034720883,0.014528783,0.24486701,0.1762236],"study_design_scores_gemma":[0.0008054701,0.0010441013,0.65671355,0.00030380604,0.00053545996,0.0036011809,0.0038612727,0.0010475108,0.0101261875,0.0067288345,0.31516737,0.00006521368],"about_ca_topic_score_codex":0.018209387,"about_ca_topic_score_gemma":0.0539177,"teacher_disagreement_score":0.018209387,"about_ca_system_score_codex":0.0021800718,"about_ca_system_score_gemma":0.0063941255,"threshold_uncertainty_score":0.03620684},"labels":[],"label_agreement":null},{"id":"W2746163443","doi":"10.1038/ng.3936","title":"Transcriptional risk scores link GWAS to eQTLs and predict complications in Crohn's disease","year":2017,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Inflammatory Bowel Disease","field":"Biochemistry, Genetics and Molecular Biology","cited_by":182,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Children's Hospital of Eastern Ontario; SickKids Foundation; University of Ottawa; Hospital for Sick Children; University of Toronto","funders":"National Institute of Diabetes and Digestive and Kidney Diseases; National Institute of General Medical Sciences; Crohn's and Colitis Foundation","keywords":"Expression quantitative trait loci; Genome-wide association study; Biology; Disease; Genetic association; Genetics; Single-nucleotide polymorphism; Gene expression profiling; Allele; Computational biology; Bioinformatics; Gene; Genotype; Gene expression; Internal medicine; Medicine","score_opus":0.008045341466057546,"score_gpt":0.26838597582014867,"score_spread":0.2603406343540911,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2746163443","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9925188,0.0010705404,0.002780312,0.00096231553,0.000097775184,0.000005307654,0.0012637058,0.0000673411,0.0012341101],"genre_scores_gemma":[0.99747366,0.00018962598,0.00094212155,0.00022870967,0.00007794586,0.0000056993654,0.0005695682,0.000027531973,0.00048497858],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9985917,0.00053956505,0.00013402117,0.00033833066,0.00021420486,0.0001821939],"domain_scores_gemma":[0.99529654,0.002382106,0.0012824151,0.00047510857,0.00025322827,0.00031056788],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0012227893,0.00075031933,0.000474054,0.0010427937,0.00044342302,0.0016169816,0.00053463934,0.0011587621,0.0041862414],"category_scores_gemma":[0.0069530574,0.0003616173,0.0014166563,0.0014525647,0.0006283587,0.0004708363,0.00082447036,0.0015471205,0.0005386493],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00086918153,0.000068532914,0.97650665,0.000060189057,0.0010224008,0.00053365703,0.000093669994,0.00090200664,0.008495095,0.00064026075,0.00069907005,0.010109339],"study_design_scores_gemma":[0.00008336044,0.00015475399,0.9882933,0.00005147991,0.0010230453,0.0010378337,0.00012607499,0.0032051355,0.0019142125,0.0028992945,0.0011783167,0.000033133485],"about_ca_topic_score_codex":0.00148721,"about_ca_topic_score_gemma":0.0016179526,"teacher_disagreement_score":0.0041862414,"about_ca_system_score_codex":0.00025103643,"about_ca_system_score_gemma":0.0002606614,"threshold_uncertainty_score":0.01400435},"labels":[],"label_agreement":null},{"id":"W2747548029","doi":"10.1038/ng.3937","title":"Cis and trans determinants of epigenetic silencing by Polycomb repressive complex 2 in Arabidopsis","year":2017,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Plant Molecular Biology Research","field":"Agricultural and Biological Sciences","cited_by":306,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Agriculture and Agri-Food Canada; Western University","funders":"Biotechnology and Biological Sciences Research Council","keywords":"PRC2; Biology; Polycomb-group proteins; Homeotic gene; Genetics; Gene silencing; Chromatin; Arabidopsis; Transcription factor; Epigenetics; Gene; Cell biology; Histone H3; Repressor","score_opus":0.02480128943399005,"score_gpt":0.29175341028611534,"score_spread":0.2669521208521253,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2747548029","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99520326,0.00073916774,0.0015571397,0.0001232776,0.000031132084,0.000007109604,0.0002611537,0.00011535357,0.0019625335],"genre_scores_gemma":[0.99714524,0.00006986474,0.00032779612,0.00005860013,0.000008147713,0.000006531356,0.00033000807,0.000048498812,0.0020052018],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9997801,0.000022258719,0.00001679532,0.00007134027,0.00006129287,0.000048272344],"domain_scores_gemma":[0.9996939,0.00006014163,0.00008211971,0.000036211615,0.000029814202,0.000097843185],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00015468444,0.0003835546,0.0003334456,0.00042307255,0.00030533932,0.0005666278,0.0003386535,0.0003156896,0.0016610824],"category_scores_gemma":[0.00021998107,0.00040072625,0.0002550582,0.00020283391,0.00031526975,0.00036335862,0.00056147575,0.0009564397,0.0005031104],"study_design_candidate":"bench_or_experimental","study_design_consensus":"bench_or_experimental","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00009116933,0.000008929547,0.00050940784,0.0000092747905,0.000003504613,0.000032160948,0.000023625602,0.000048572656,0.998334,0.00020594525,0.000028383645,0.0007051459],"study_design_scores_gemma":[0.00007916288,0.00017919039,0.12614922,0.000009001682,0.0000701054,0.000465417,0.00027442665,0.0046302835,0.8642082,0.0006708124,0.0032219852,0.00004230839],"about_ca_topic_score_codex":0.0024602881,"about_ca_topic_score_gemma":0.005592531,"teacher_disagreement_score":0.0024602881,"about_ca_system_score_codex":0.0007492786,"about_ca_system_score_gemma":0.00021219306,"threshold_uncertainty_score":0.0055568814},"labels":[],"label_agreement":null},{"id":"W2748552522","doi":"10.1038/ng.3933","title":"Mutations in KEOPS-complex genes cause nephrotic syndrome with primary microcephaly","year":2017,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Renal Diseases and Glomerulopathies","field":"Medicine","cited_by":221,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Hospital for Sick Children; SickKids Foundation; University of Toronto; Centre Hospitalier Universitaire Sainte-Justine; London Health Sciences Centre; Western University; Université de Montréal; McGill University Health Centre","funders":"Common Fund; Eunice Kennedy Shriver National Institute of Child Health and Human Development; National Institute of Environmental Health Sciences; National Institute of General Medical Sciences; National Human Genome Research Institute; National Institutes of Health; Deutsche Akademie der Naturforscher Leopoldina - Nationale Akademie der Wissenschaften; Vlaamse regering; Hospital for Sick Children; Université de Montréal; Tehran University of Medical Sciences and Health Services; Yale University; University of Toronto; Hacettepe Üniversitesi; Fonds de Recherche du Québec - Santé; Ministry of Science, ICT and Future Planning; University of Bristol; Nierstichting; Max-Planck-Gesellschaft; Yonsei University; Agence Nationale de la Recherche; Yonsei University College of Medicine; McGill University; Deutsche Forschungsgemeinschaft; European Commission; National Institute for Health and Care Research; National Research Foundation; National Center for Advancing Translational Sciences; National Research Foundation of Korea; National Research Foundation Singapore; King's College London; Sociedad Española de Nefrología; National Institute of Diabetes and Digestive and Kidney Diseases; ASN Foundation for Kidney Research; King's College Hospital NHS Foundation Trust; National Science Foundation","keywords":"Microcephaly; Biology; Gene knockdown; Endoplasmic reticulum; Phenotype; Genetics; Unfolded protein response; Gene; Cell biology; Cancer research","score_opus":0.015792783645416125,"score_gpt":0.28710954104147324,"score_spread":0.2713167573960571,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2748552522","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99235415,0.000633043,0.0015626414,0.00056660385,0.00016040169,0.000041442017,0.00044213102,0.00012350715,0.004116065],"genre_scores_gemma":[0.9976362,0.00014713118,0.0010106495,0.00010817985,0.000083758176,0.00000942622,0.00010941319,0.000043946773,0.00085125474],"study_design_codex":"case_report","study_design_gemma":"observational","domain_scores_codex":[0.9994267,0.000058480007,0.000090695925,0.000109144654,0.00022112831,0.00009390337],"domain_scores_gemma":[0.99868387,0.0004610469,0.00038241514,0.00004796208,0.00006276541,0.00036202488],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00019828344,0.0017770547,0.0005881668,0.0015255437,0.00081098604,0.0005337877,0.00084670767,0.0018649704,0.0030406902],"category_scores_gemma":[0.0016929068,0.00040011053,0.0006140232,0.0010246339,0.0014697068,0.00044076404,0.0013320746,0.000883955,0.00041199886],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.000758195,0.00014129565,0.048898976,0.00015644418,0.00042204818,0.77653027,0.00062891835,0.001338865,0.15793224,0.002292916,0.0021122582,0.008787608],"study_design_scores_gemma":[0.00024470076,0.00021832426,0.17914422,0.00007396581,0.0004683677,0.7638541,0.0004050832,0.0032141532,0.044969864,0.0022867024,0.00500732,0.00011331051],"about_ca_topic_score_codex":0.0028933673,"about_ca_topic_score_gemma":0.0046993895,"teacher_disagreement_score":0.0030406902,"about_ca_system_score_codex":0.0005919464,"about_ca_system_score_gemma":0.0006893392,"threshold_uncertainty_score":0.010172188},"labels":[],"label_agreement":null},{"id":"W2749641460","doi":"10.1038/ng.3934","title":"A mutational signature reveals alterations underlying deficient homologous recombination repair in breast cancer","year":2017,"lang":"en","type":"article","venue":"Nature Genetics","topic":"BRCA gene mutations in cancer","field":"Biochemistry, Genetics and Molecular Biology","cited_by":549,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"McGill University Health Centre; McGill University","funders":"National Cancer Institute; National Institute for Health and Care Research; Cancer Research UK","keywords":"Biology; PALB2; Frameshift mutation; Homologous recombination; Genetics; BRCA2 Protein; Breast cancer; Germline; CHEK2; MSH2; Heteroduplex; Missense mutation; Germline mutation; DNA repair; DNA mismatch repair; Mutation; Cancer; Gene","score_opus":0.018343988985080984,"score_gpt":0.3277831247906727,"score_spread":0.3094391358055917,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2749641460","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9977448,0.0003937585,0.0005471553,0.00006336404,0.000009387018,0.000008152768,0.00034456988,0.000063379455,0.00082545955],"genre_scores_gemma":[0.99888545,0.00020246659,0.0003048391,0.000024689647,0.0000052058276,0.00000371654,0.00019181478,0.000011002791,0.00037078472],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.99992085,0.000007985222,0.000009128389,0.000016104737,0.000024360508,0.000021549617],"domain_scores_gemma":[0.99986184,0.00001996046,0.000057519323,0.000012685679,0.000013200256,0.000034742672],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00007568417,0.00025487688,0.00019543545,0.00086933386,0.00015292136,0.00024470693,0.00018693524,0.000416534,0.0014029639],"category_scores_gemma":[0.00018898853,0.00013996747,0.00018710215,0.00039232048,0.0001518331,0.00011977936,0.00018193727,0.0002177619,0.00031967746],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00036735323,0.000027906131,0.005393873,0.000024951778,0.000020915084,0.0021680964,0.00002276987,0.00014505476,0.9889764,0.00019372818,0.00011786819,0.0025411136],"study_design_scores_gemma":[0.00004536717,0.00050531956,0.21856527,0.000015745964,0.00016679395,0.045540765,0.00010151096,0.0018560546,0.7291966,0.00047762008,0.0035060532,0.000022801041],"about_ca_topic_score_codex":0.00046332536,"about_ca_topic_score_gemma":0.00042071496,"teacher_disagreement_score":0.0014029639,"about_ca_system_score_codex":0.0001408616,"about_ca_system_score_gemma":0.00011890085,"threshold_uncertainty_score":0.004693389},"labels":[],"label_agreement":null},{"id":"W2751430583","doi":"10.1038/ng.3949","title":"Identification of 153 new loci associated with heel bone mineral density and functional involvement of GPC6 in osteoporosis","year":2017,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Genetic Associations and Epidemiology","field":"Biochemistry, Genetics and Molecular Biology","cited_by":517,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"McGill University Health Centre; McGill University; University of Toronto; Jewish General Hospital","funders":"National Health and Medical Research Council; Fonds de Recherche du Québec - Santé; Natural Sciences and Engineering Research Council of Canada; Canadian Institutes of Health Research; National Institutes of Health; National Institute of Arthritis and Musculoskeletal and Skin Diseases; Medical Research Council; Versus Arthritis; National Institute for Health and Care Research; Jewish General Hospital; Ernest Heine Family Foundation; Uppsala Universitet; Vetenskapsrådet; ZonMw; European Commission; Genome Canada; British Heart Foundation; Wellcome Trust","keywords":"Biology; Genome-wide association study; Single-nucleotide polymorphism; Phenotype; Genetics; Osteoporosis; Genetic association; Gene; Quantitative trait locus; Candidate gene; Bone mineral; Expression quantitative trait loci; Endocrinology; Genotype","score_opus":0.01253517862794562,"score_gpt":0.2525917661583964,"score_spread":0.24005658753045078,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2751430583","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99760073,0.0003859285,0.0008776022,0.000060704046,0.000013882783,0.00001317234,0.000533818,0.000016850168,0.00049737445],"genre_scores_gemma":[0.99706036,0.00016545915,0.0012949934,0.00004873233,0.00002145011,0.000012611711,0.0006655368,0.000012252002,0.0007185858],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99957496,0.00007016059,0.000045118173,0.00010953166,0.0001341393,0.00006605733],"domain_scores_gemma":[0.9990891,0.000453669,0.00019919741,0.00007152836,0.00007134918,0.000115102055],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0003636589,0.00043118797,0.00050749985,0.0016625426,0.0004363654,0.0005218253,0.0005721822,0.00076140853,0.0027531283],"category_scores_gemma":[0.0013312554,0.00022983934,0.00062493165,0.0017001,0.00040752804,0.00015831932,0.0003279149,0.000599389,0.00031620046],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0044757384,0.0002803074,0.6714764,0.00026020946,0.0011034897,0.018212717,0.0010182994,0.001284632,0.26163754,0.0011190668,0.001041301,0.038090352],"study_design_scores_gemma":[0.0001840239,0.00028759686,0.9657878,0.000033584267,0.00038750394,0.010316168,0.00017003788,0.0015402401,0.018124415,0.0005041089,0.0026311493,0.0000332177],"about_ca_topic_score_codex":0.0028688551,"about_ca_topic_score_gemma":0.002371233,"teacher_disagreement_score":0.0028688551,"about_ca_system_score_codex":0.00024296701,"about_ca_system_score_gemma":0.00019257129,"threshold_uncertainty_score":0.009210169},"labels":[],"label_agreement":null},{"id":"W2751722940","doi":"10.1038/ng.3943","title":"Identification of new susceptibility loci for type 2 diabetes and shared etiological pathways with coronary heart disease","year":2017,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Genetic Associations and Epidemiology","field":"Biochemistry, Genetics and Molecular Biology","cited_by":298,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"McMaster University","funders":"National Institute of Diabetes and Digestive and Kidney Diseases; Medical Research Council; National Institutes of Health; Novo Nordisk Fonden; Sydäntutkimussäätiö; Ministry of Education, Culture, Sports, Science and Technology; British Heart Foundation; National Center for Advancing Translational Sciences; Wellcome Trust; National Institute of Neurological Disorders and Stroke; National Institute for Health and Care Research; Regeneron Pharmaceuticals; Foundation for Cardiovascular Research; NIHR Cambridge Biomedical Research Centre; European Commission; McMaster University; Fogarty International Center; National Heart, Lung, and Blood Institute; Pfizer; Eli Lilly and Company; Andrea and Charles Bronfman Philanthropies; American Heart Association","keywords":"Biology; Identification (biology); Type 2 diabetes; Genetics; Etiology; Disease; Coronary heart disease; Diabetes mellitus; Heart disease; Computational biology; Bioinformatics; Internal medicine; Endocrinology; Medicine","score_opus":0.025982250746192776,"score_gpt":0.3018202284620115,"score_spread":0.27583797771581875,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2751722940","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9952992,0.0013160388,0.0017636318,0.00040180498,0.000046120644,0.000009872705,0.00030623007,0.000025265881,0.00083167123],"genre_scores_gemma":[0.9960448,0.0006243091,0.0021144077,0.00010275282,0.00015904244,0.000012090147,0.00034987653,0.000016940243,0.00057574804],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9988972,0.00036905566,0.00011412702,0.00029573965,0.000192837,0.00013117361],"domain_scores_gemma":[0.9974734,0.000802516,0.00073377666,0.00042853047,0.00022033777,0.00034137844],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0012867331,0.0007697054,0.00063398527,0.0018616944,0.00048820674,0.0014228461,0.0009394519,0.0010740289,0.0028387683],"category_scores_gemma":[0.0029723549,0.0005888414,0.001086304,0.0019654087,0.00064305315,0.0005728621,0.0008517267,0.0012511732,0.00025491137],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0012207294,0.0002098324,0.9731406,0.000047491703,0.00090953923,0.0016956752,0.00021081262,0.00027917512,0.011999303,0.00093099114,0.00027630496,0.009079502],"study_design_scores_gemma":[0.00014588446,0.00017457387,0.98952335,0.000021621448,0.0007499387,0.003572238,0.00022600114,0.0011323001,0.0017085642,0.0020022476,0.0007208686,0.000022476876],"about_ca_topic_score_codex":0.0017509968,"about_ca_topic_score_gemma":0.0015451491,"teacher_disagreement_score":0.0028387683,"about_ca_system_score_codex":0.00026484116,"about_ca_system_score_gemma":0.00037116653,"threshold_uncertainty_score":0.009496629},"labels":[],"label_agreement":null},{"id":"W2752299790","doi":"10.1038/ng.3947","title":"A functional genomics predictive network model identifies regulators of inflammatory bowel disease","year":2017,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Inflammatory Bowel Disease","field":"Biochemistry, Genetics and Molecular Biology","cited_by":271,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Toronto","funders":"National Institute of Allergy and Infectious Diseases; National Human Genome Research Institute; National Institute of Mental Health; National Institute of Diabetes and Digestive and Kidney Diseases; National Heart, Lung, and Blood Institute; National Institute on Aging; National Institutes of Health","keywords":"Inflammatory bowel disease; Genome-wide association study; Biology; Computational biology; Disease; Gene regulatory network; Genomics; Systems biology; Genetic association; Genome; Genetics; Gene; Medicine; Single-nucleotide polymorphism; Gene expression","score_opus":0.005918687323338161,"score_gpt":0.2263174284773962,"score_spread":0.22039874115405803,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2752299790","genre_codex":"methods","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":null,"domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.41362554,0.00070064527,0.56334716,0.0034705517,0.00008958445,0.00014227035,0.0044855084,0.0012049717,0.012933776],"genre_scores_gemma":[0.972585,0.00025526,0.022930605,0.00014234919,0.00004031892,0.00009538078,0.0012349674,0.000037173544,0.0026788025],"study_design_codex":"simulation_or_modeling","study_design_gemma":"simulation_or_modeling","domain_scores_codex":[0.999684,0.000121168414,0.0000072788525,0.000107966924,0.00004377628,0.000035953075],"domain_scores_gemma":[0.99916756,0.00056219596,0.000088104425,0.000042038384,0.000090057445,0.000050006725],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0007593655,0.0006687801,0.00051552337,0.0009707618,0.00029959122,0.00085907534,0.0009792355,0.000573027,0.003519319],"category_scores_gemma":[0.0023568626,0.0002335764,0.0006307915,0.0006623107,0.0004168498,0.0008044779,0.00046146289,0.0006318833,0.00031073194],"study_design_candidate":"simulation_or_modeling","study_design_consensus":"simulation_or_modeling","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00042653657,0.00022743651,0.014595713,0.00009994898,0.00019951981,0.0003718525,0.00006894194,0.8979866,0.0061622867,0.04656951,0.0025603988,0.030731278],"study_design_scores_gemma":[0.000018165138,0.000028032247,0.0014371995,0.0000045689735,0.0000444588,0.00003347871,0.000009184327,0.9793021,0.00031826302,0.018455362,0.00034479448,0.000004269838],"about_ca_topic_score_codex":0.006533177,"about_ca_topic_score_gemma":0.006893669,"teacher_disagreement_score":0.006533177,"about_ca_system_score_codex":0.00088785787,"about_ca_system_score_gemma":0.00093373004,"threshold_uncertainty_score":0.012990296},"labels":[],"label_agreement":null},{"id":"W2763010484","doi":"10.1038/ng.3970","title":"Contribution of rare inherited and de novo variants in 2,871 congenital heart disease probands","year":2017,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Congenital heart defects research","field":"Biochemistry, Genetics and Molecular Biology","cited_by":928,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"SickKids Foundation; Hospital for Sick Children; University of Toronto","funders":"Eunice Kennedy Shriver National Institute of Child Health and Human Development; National Institute of General Medical Sciences; National Center for Advancing Translational Sciences; National Human Genome Research Institute; National Heart, Lung, and Blood Institute; National Institutes of Health","keywords":"Proband; Biology; Genetics; Exome sequencing; Heart disease; Exome; Tetralogy of Fallot; Mutation; Gene; Internal medicine; Medicine","score_opus":0.009479004487232271,"score_gpt":0.3019473565400703,"score_spread":0.29246835205283805,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2763010484","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9970427,0.0006433932,0.00044580188,0.00011104508,0.000045563513,0.000016099126,0.00054013176,0.00003890232,0.0011164446],"genre_scores_gemma":[0.99821496,0.00022419152,0.000506689,0.000059431357,0.00006466581,0.000012774893,0.00037861825,0.00004367703,0.0004950611],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9983506,0.00027250062,0.00026143552,0.0005195437,0.00039290963,0.0002030452],"domain_scores_gemma":[0.99764806,0.0012490242,0.0004501765,0.0001256638,0.00016414929,0.00036292567],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0005548949,0.0015469873,0.0008547699,0.0029230523,0.0014782604,0.0012495202,0.001069218,0.0017034231,0.0058312467],"category_scores_gemma":[0.004283894,0.00056429784,0.0008445784,0.0014194605,0.0007854451,0.00040193656,0.0008779094,0.00096377695,0.00084944675],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0022323437,0.00036427047,0.7454706,0.00022792518,0.00066831155,0.16624492,0.0020942297,0.0010152722,0.056020085,0.001390529,0.0012857384,0.022985874],"study_design_scores_gemma":[0.00027958103,0.0005513597,0.72727495,0.0002192691,0.0011817733,0.2492233,0.0011762924,0.0027204098,0.010405453,0.0016547237,0.0052191117,0.00009377812],"about_ca_topic_score_codex":0.0029721118,"about_ca_topic_score_gemma":0.0026138967,"teacher_disagreement_score":0.0058312467,"about_ca_system_score_codex":0.0003755363,"about_ca_system_score_gemma":0.00043165026,"threshold_uncertainty_score":0.019507468},"labels":[],"label_agreement":null},{"id":"W2767038995","doi":"10.1038/ng.3977","title":"Exome-wide association study of plasma lipids in >300,000 individuals","year":2017,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Lipid metabolism and disorders","field":"Medicine","cited_by":595,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Université de Montréal; Montreal Heart Institute","funders":"FP7 Ideas: European Research Council; National Institute of General Medical Sciences; National Cancer Institute; National Human Genome Research Institute; National Heart, Lung, and Blood Institute; National Center for Advancing Translational Sciences; Medical Research Council; Directorate for Biological Sciences; Novo Nordisk Fonden; Faculty of Health and Medical Sciences, University of Western Australia; Rigshospitalet; British Heart Foundation; NIHR Exeter Clinical Research Facility; European Hematology Association; Sarnoff Cardiovascular Research Foundation; Perelman School of Medicine, University of Pennsylvania; Vanderbilt University Medical Center; Steno Diabetes Center Copenhagen; Wellcome Trust; National Institutes of Health; Regeneron Pharmaceuticals; Lundbeckfonden; Eli Lilly and Company; AstraZeneca; National Institute for Health and Care Research; Quest Diagnostics; Gentofte Hospital; Bayer HealthCare; Donovan Family Foundation; National Institute on Drug Abuse; University of Pennsylvania; Japanese Circulation Society; Vanderbilt University; Alnylam Pharmaceuticals; Massachusetts General Hospital; Broad Institute; National Institute of Diabetes and Digestive and Kidney Diseases; Sanofi; U.S. Department of Health and Human Services","keywords":"Biology; Internal medicine; Endocrinology; Allele; Exome; Genome-wide association study; Coronary artery disease; High-density lipoprotein; Cholesterol; Lipolysis; Type 2 diabetes; Genotyping; Single-nucleotide polymorphism; Lipoprotein; Genetics; Exome sequencing; Diabetes mellitus; Genotype; Gene; Medicine; Adipose tissue; Phenotype","score_opus":0.01307542389857536,"score_gpt":0.29132034573823773,"score_spread":0.2782449218396624,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2767038995","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9942457,0.00060558046,0.00039982516,0.00014308917,0.000022407621,0.000009011255,0.0039647995,0.000026141612,0.0005834365],"genre_scores_gemma":[0.9964682,0.0001898119,0.00031573963,0.00008907492,0.000017627932,0.000012345694,0.0020676125,0.000018573017,0.0008210206],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9991493,0.00018768094,0.000092187016,0.0003736041,0.000099136705,0.00009812199],"domain_scores_gemma":[0.9993729,0.00019293895,0.00013706757,0.00014992878,0.000056280856,0.000090876325],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00087387796,0.00053423055,0.0006560895,0.000673756,0.0007224597,0.0008076598,0.00045298296,0.0009895916,0.002325281],"category_scores_gemma":[0.0019582505,0.0004917322,0.00080662605,0.0017514002,0.00033124042,0.0004232613,0.00067177415,0.00065526494,0.00046007402],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0021423965,0.000087500426,0.9764583,0.00006609069,0.0018493931,0.0012086574,0.00028719575,0.00038281232,0.00930317,0.00024450745,0.0023615747,0.005608432],"study_design_scores_gemma":[0.000112888454,0.0000804586,0.99495935,0.000012562303,0.0007269738,0.0009371527,0.0001125112,0.00051786005,0.000473297,0.00018790383,0.0018644742,0.000014498917],"about_ca_topic_score_codex":0.009367976,"about_ca_topic_score_gemma":0.011320386,"teacher_disagreement_score":0.009367976,"about_ca_system_score_codex":0.0002654914,"about_ca_system_score_gemma":0.00027589893,"threshold_uncertainty_score":0.018626869},"labels":[],"label_agreement":null},{"id":"W2775986795","doi":"10.1038/s41588-017-0019-2","title":"Bacterial genomics of plant adaptation","year":2017,"lang":"en","type":"letter","venue":"Nature Genetics","topic":"Plant Pathogenic Bacteria Studies","field":"Agricultural and Biological Sciences","cited_by":0,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Canada's Michael Smith Genome Sciences Centre; University of British Columbia","funders":"","keywords":"Biology; Genomics; Comparative genomics; Adaptation (eye); Genetics; Evolutionary biology; Computational biology; Genome; Gene","score_opus":0.024417587652893785,"score_gpt":0.21270629000743435,"score_spread":0.18828870235454057,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2775986795","genre_codex":"commentary","genre_gemma":"other","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"other","genre_consensus":null,"domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.000695413,0.0018245049,0.00017774418,0.96259356,0.030549169,0.0000090434905,0.000036667865,0.00002858462,0.0040853214],"genre_scores_gemma":[0.012112088,0.0019344321,0.00019005631,0.9100507,0.059407007,0.000037692047,0.00004895926,0.000028375278,0.016190585],"study_design_codex":"not_applicable","study_design_gemma":"not_applicable","domain_scores_codex":[0.99839646,0.0003669899,0.000093924195,0.00016803305,0.0006239281,0.00035072467],"domain_scores_gemma":[0.9940796,0.0035987725,0.00026319202,0.00026227295,0.00073826313,0.0010578999],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0027950797,0.00047756132,0.00075077923,0.00036761496,0.0027835923,0.0024626332,0.0011099613,0.0307109,0.005190954],"category_scores_gemma":[0.012405597,0.0004618039,0.00068591186,0.00022899218,0.0029965448,0.002010344,0.0018122421,0.030417245,0.0032391008],"study_design_candidate":"not_applicable","study_design_consensus":"not_applicable","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00010831903,0.000045802437,0.00039995243,0.000029005441,0.000013241213,0.00094459066,0.00009666277,0.000070215036,0.0005231718,0.007028934,0.97794944,0.012790627],"study_design_scores_gemma":[0.0001901169,0.00009952493,0.0014847751,0.00012739304,0.000036062593,0.0007970248,0.00023615909,0.00054279616,0.0010911954,0.024858806,0.97049004,0.000046170175],"about_ca_topic_score_codex":0.0032053294,"about_ca_topic_score_gemma":0.0058437963,"teacher_disagreement_score":0.0307109,"about_ca_system_score_codex":0.0025692254,"about_ca_system_score_gemma":0.002540524,"threshold_uncertainty_score":0.018641174},"labels":[],"label_agreement":null},{"id":"W2780232486","doi":"10.1038/s41588-017-0014-7","title":"Multiancestry association study identifies new asthma risk loci that colocalize with immune-cell enhancer marks","year":2017,"lang":"en","type":"review","venue":"Nature Genetics","topic":"Asthma and respiratory diseases","field":"Medicine","cited_by":592,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Centre Intégré Universitaire de Santé et de Services Sociaux du Saguenay–Lac-Saint-Jean; University of Alberta; Université du Québec à Chicoutimi; Ontario Institute for Cancer Research; McGill University and Génome Québec Innovation Centre; University of British Columbia; University of Manitoba","funders":"National Heart, Lung, and Blood Institute; Medical Research Council; National Institute of Environmental Health Sciences; National Institute for Health and Care Research; National Cancer Institute; Lundbeckfonden; Wellcome Trust","keywords":"Asthma; Biology; Genome-wide association study; Pleiotropy; Genetics; Immunology; Genetic association; Enhancer; Immune system; Genotype; Gene; Phenotype; Single-nucleotide polymorphism; Transcription factor","score_opus":0.02818965865637482,"score_gpt":0.35267247185170564,"score_spread":0.32448281319533084,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2780232486","genre_codex":"review","genre_gemma":"review","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"review","genre_consensus":"review","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.0014252326,0.9949174,0.00090234465,0.0010090051,0.0002493424,0.00000537458,0.00009089623,0.000023104283,0.0013774318],"genre_scores_gemma":[0.014896344,0.9803272,0.0013568464,0.0011509494,0.00055509654,0.000014309267,0.0002629332,0.0000069881667,0.0014293808],"study_design_codex":"design_other","study_design_gemma":"observational","domain_scores_codex":[0.9998056,0.000029157858,0.00002333603,0.000060574042,0.00005924148,0.00002203721],"domain_scores_gemma":[0.9996106,0.00019320675,0.00007843114,0.000016449501,0.000063834705,0.000037463946],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00057230494,0.0007080832,0.0011402131,0.0011059253,0.00015054688,0.0006412009,0.0008478747,0.0010666634,0.0021585359],"category_scores_gemma":[0.00067679875,0.00021898851,0.00047600653,0.001124804,0.00037054587,0.0004576249,0.00061884697,0.0012985949,0.0006395491],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0002446388,0.000054166823,0.0076538273,0.010748952,0.00070512074,0.00145413,0.00011798502,0.0005155795,0.011038193,0.005205893,0.025271816,0.9369898],"study_design_scores_gemma":[0.00013233496,0.00014526417,0.027780041,0.0034494633,0.0021987928,0.008897555,0.00018462977,0.0004043626,0.0046028625,0.009092082,0.94303006,0.00008268036],"about_ca_topic_score_codex":0.0006708324,"about_ca_topic_score_gemma":0.0014592168,"teacher_disagreement_score":0.0021585359,"about_ca_system_score_codex":0.00036293833,"about_ca_system_score_gemma":0.00066769397,"threshold_uncertainty_score":0.0072209835},"labels":[],"label_agreement":null},{"id":"W2780667489","doi":"10.1038/s41588-017-0011-x","title":"Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity","year":2017,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Diet and metabolism studies","field":"Medicine","cited_by":428,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"York University; Université de Montréal; Dalhousie University; Montreal Heart Institute","funders":"FP7 Ideas: European Research Council; Carolina Population Center, University of North Carolina at Chapel Hill; National Institute of Child Health and Human Development; National Institute of Environmental Health Sciences; National Institute of Neurological Disorders and Stroke; National Center for Research Resources; National Institute of General Medical Sciences; National Human Genome Research Institute; National Institute on Drug Abuse; National Institute on Aging; National Institute of Diabetes and Digestive and Kidney Diseases; Norwegian Institute of Public Health; Danish Agency for Science and Higher Education; National Health and Medical Research Council; National Heart, Lung, and Blood Institute; Biotechnology and Biological Sciences Research Council; Canadian Institutes of Health Research; Forsknings- og Innovationsstyrelsen; Directorate for Biological Sciences; National Institutes of Health; Diabetesforeningen; MRC-PHE Centre for Environment and Health; Centre for Cognitive Ageing and Cognitive Epidemiology; H. Lundbeck A/S; Hjartavernd; Institut de Cardiologie de Montréal; Fondation Institut de Cardiologie de Montréal; Medical Research Council; Servier; Regione Lombardia; Boehringer Ingelheim Stiftung; National Center for Advancing Translational Sciences; Economic and Social Research Council; Università degli Studi di Verona; Fondation Leenaards; A.P. Møller og Hustru Chastine Mc-Kinney Møllers Fond til almene Formaal; Sydäntutkimussäätiö; Universitetet i Bergen; Aarhus Universitets Forskningsfond; Max-Planck-Gesellschaft; Deutsche Forschungsgemeinschaft; Nederlandse Organisatie voor Wetenschappelijk Onderzoek; Ministero della Salute; Region Hovedstaden; European Hematology Association; Novo Nordisk; British Heart Foundation; Bundesministerium für Bildung und Forschung; Strategiske Forskningsråd; ZonMw; SystemsX.ch; Schweizerischer Nationalfonds zur Förderung der Wissenschaftlichen Forschung; European Foundation for the Study of Diabetes; Cancer Research UK; National University of Singapore; Imperial College Healthcare NHS Trust; Wellcome Trust; Aarhus Universitet; Australian Government; Norges Forskningsråd; QIMR Berghofer Medical Research Institute; AstraZeneca; National Institute for Health Research Health Protection Research Unit; European Commission; Steno Diabetes Center Copenhagen; Norges Teknisk-Naturvitenskapelige Universitet; Wake Forest School of Medicine; Helse Vest; Johns Hopkins University; Sundhed og Sygdom, Det Frie Forskningsråd; National Cancer Institute; Lundbeckfonden; Foundation for Cardiovascular Research; Queen Mary University of London; National Institute for Health and Care Research; National Science Foundation; Massachusetts General Hospital; Istituto Superiore di Sanità; Imperial College London; Eunice Kennedy Shriver National Institute of Child Health and Human Development; GlaxoSmithKline; Erasmus Medisch Centrum; Andrea and Charles Bronfman Philanthropies; Novo Nordisk Fonden; American Heart Association; Diabetesforbundet; Pfizer","keywords":"Biology; Body mass index; Obesity; Energy expenditure; Genetics; Energy metabolism; Endocrinology; Internal medicine","score_opus":0.014085865331733324,"score_gpt":0.24969705725861865,"score_spread":0.23561119192688534,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2780667489","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9661154,0.02147829,0.0062121963,0.0007413918,0.000110463,0.000033457727,0.0033414918,0.00014156944,0.0018257903],"genre_scores_gemma":[0.9934076,0.0029119854,0.0015874227,0.00023770728,0.00005508324,0.0000184059,0.0013413782,0.000032505777,0.00040779993],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99940264,0.0001199903,0.000058200414,0.0002469359,0.00011407114,0.00005812221],"domain_scores_gemma":[0.9991966,0.00037770715,0.00023886959,0.00008697436,0.000043618944,0.000056348148],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0006542965,0.0006036093,0.00069669395,0.0011549366,0.0004469966,0.00075984903,0.00033126128,0.0005794543,0.0029775936],"category_scores_gemma":[0.0015355955,0.00022361669,0.0013578235,0.0019376499,0.0004898536,0.00025048607,0.0005479716,0.00081776996,0.0002303907],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0046280846,0.000122637,0.8445641,0.0009124649,0.018044688,0.0025409693,0.00029029106,0.00201694,0.07326398,0.0011982046,0.0014721276,0.050945554],"study_design_scores_gemma":[0.000095261894,0.000118599215,0.98547804,0.00008507414,0.004330468,0.0015293431,0.00008592573,0.001238634,0.0028135593,0.0015709962,0.0026329993,0.000021111093],"about_ca_topic_score_codex":0.003160452,"about_ca_topic_score_gemma":0.0042029265,"teacher_disagreement_score":0.003160452,"about_ca_system_score_codex":0.00021713866,"about_ca_system_score_gemma":0.00023055902,"threshold_uncertainty_score":0.009961009},"labels":[],"label_agreement":null},{"id":"W2780728213","doi":"10.1038/s41588-018-0262-1","title":"Comparative genomics of the major parasitic worms","year":2018,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Parasite Biology and Host Interactions","field":"Environmental Science","cited_by":610,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Toronto; SickKids Foundation; Hospital for Sick Children; Canada Research Chairs; University of Calgary; McGill University","funders":"National Institute of General Medical Sciences; Biologické Centrum, Akademie Věd České Republiky; Biotechnology and Biological Sciences Research Council; National Institute of Allergy and Infectious Diseases; Medical Research Council; Natural Sciences and Engineering Research Council of Canada; Directorate for Biological Sciences; National Institutes of Health; National Human Genome Research Institute; Wellcome Trust; Universitas Indonesia; Rural and Environment Science and Analytical Services Division; Scottish Government; University of Toronto; European Molecular Biology Laboratory; European Bioinformatics Institute; Compute Canada; James Hutton Institute","keywords":"Biology; Genomics; Genome; Comparative genomics; Gene family; In silico; Phylogenetics; Gene; Parasitism; Host (biology); Evolutionary biology; Genetics; Computational biology","score_opus":0.013580974020612637,"score_gpt":0.3273898508689441,"score_spread":0.3138088768483315,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2780728213","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9794661,0.0036372265,0.0032293429,0.00019566044,0.000015943737,0.000026234911,0.008093601,0.00008842646,0.00524738],"genre_scores_gemma":[0.95718616,0.003918634,0.009016744,0.00018344446,0.000024749204,0.000042637046,0.026470512,0.00006900351,0.003088152],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.99988186,0.000015433414,0.0000060775087,0.00003971963,0.000030740113,0.000026195201],"domain_scores_gemma":[0.9998061,0.000045702305,0.00004869552,0.00001686973,0.000034019795,0.000048672493],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00014765223,0.00024820832,0.00030233111,0.0008928457,0.0003461998,0.0004175205,0.00019604409,0.0003117292,0.0013228398],"category_scores_gemma":[0.0002580357,0.00011349079,0.0003200199,0.0012282014,0.000168785,0.00030059484,0.00032865288,0.0003436101,0.00038828276],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00039793467,0.000053540785,0.00827151,0.00027269823,0.000059727638,0.00024492256,0.00029918068,0.00064816896,0.9636581,0.000811161,0.00039032928,0.024892787],"study_design_scores_gemma":[0.000034861478,0.00085239636,0.8588329,0.00009571619,0.00024633243,0.0024075478,0.0008390615,0.003634918,0.08932561,0.0020484864,0.041630954,0.000051349263],"about_ca_topic_score_codex":0.0019177931,"about_ca_topic_score_gemma":0.0020018353,"teacher_disagreement_score":0.0019177931,"about_ca_system_score_codex":0.00027491324,"about_ca_system_score_gemma":0.00026663774,"threshold_uncertainty_score":0.004425347},"labels":[],"label_agreement":null},{"id":"W2782908004","doi":"10.1038/s41588-018-0041-z","title":"Pan-genome analysis highlights the extent of genomic variation in cultivated and wild rice","year":2018,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Genetic Mapping and Diversity in Plants and Animals","field":"Biochemistry, Genetics and Molecular Biology","cited_by":693,"is_retracted":false,"has_abstract":true,"route_ca_aff":false,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"","funders":"Institute of Genetics; National Natural Science Foundation of China; Chinese Academy of Sciences; Ministry of Education, Culture, Sports, Science and Technology","keywords":"Biology; Oryza rufipogon; Oryza sativa; Genome; Genetics; Structural variation; Whole genome sequencing; Japonica; Genetic variation; Genomics; Quantitative trait locus; Oryza; Reference genome; Genetic diversity; Gene; Population; Botany","score_opus":0.006164265004969497,"score_gpt":0.22224821047110574,"score_spread":0.21608394546613624,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2782908004","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.975669,0.0014302422,0.007747704,0.000101333026,0.000013584416,0.000008733132,0.01306468,0.00030575565,0.001658928],"genre_scores_gemma":[0.9641876,0.00076703704,0.010503968,0.00013595588,0.000016318243,0.00002633404,0.023555558,0.00015347339,0.00065365614],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.99975294,0.000020085337,0.000014557605,0.00015200103,0.00003237536,0.000028051956],"domain_scores_gemma":[0.9997013,0.00009298771,0.00007218956,0.00006804392,0.000027084538,0.000038338705],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0002686247,0.00019635595,0.0003498069,0.0011439981,0.00023523202,0.00044019424,0.00019404231,0.00019848885,0.0012259801],"category_scores_gemma":[0.0004248591,0.00012858084,0.0003683424,0.0017035478,0.00017742647,0.0003297727,0.0005432144,0.0003878671,0.00018518514],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0006550693,0.000054553195,0.092328236,0.0004246896,0.00058898807,0.00036652433,0.00046509018,0.0016692122,0.84615266,0.0012223393,0.0010892928,0.054983348],"study_design_scores_gemma":[0.00001640039,0.00006765461,0.9605158,0.000020795005,0.00020086946,0.00052041333,0.00015824405,0.002776197,0.019475413,0.0014038356,0.014824554,0.000019837831],"about_ca_topic_score_codex":0.0013804842,"about_ca_topic_score_gemma":0.0035944514,"teacher_disagreement_score":0.0013804842,"about_ca_system_score_codex":0.0001867765,"about_ca_system_score_gemma":0.00015308053,"threshold_uncertainty_score":0.0041012764},"labels":[],"label_agreement":null},{"id":"W2783335334","doi":"10.1038/s41588-017-0035-2","title":"Pioneer factor Pax7 deploys a stable enhancer repertoire for specification of cell fate","year":2018,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Genomics and Chromatin Dynamics","field":"Biochemistry, Genetics and Molecular Biology","cited_by":181,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"McGill University and Génome Québec Innovation Centre; McGill University; Montreal Clinical Research Institute","funders":"","keywords":"Biology; Enhancer; Chromatin; Epigenetics; Cell fate determination; DNA methylation; Chromatin remodeling; Cell biology; Transcription factor; Genetics; DNA; Gene; Gene expression","score_opus":0.006971573291339544,"score_gpt":0.2389681770935809,"score_spread":0.23199660380224135,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2783335334","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.97464246,0.0009703857,0.017761925,0.00018451591,0.00006392993,0.000012972285,0.00014743545,0.00043440526,0.0057820287],"genre_scores_gemma":[0.99349725,0.00022597284,0.0027593721,0.000059023347,0.00001567689,0.000009610491,0.00016737521,0.00015059914,0.003115127],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9996884,0.000019867592,0.000009889223,0.000067466404,0.00014064746,0.00007377075],"domain_scores_gemma":[0.9997044,0.00006479121,0.000047322406,0.00006699789,0.000037039714,0.000079446945],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00032030162,0.00021869534,0.00025838354,0.00038119525,0.00031245343,0.0006852725,0.00050587155,0.00039873368,0.0021303701],"category_scores_gemma":[0.00039462678,0.00044739796,0.0002062403,0.0001719602,0.0005643167,0.0005158532,0.00094747636,0.001001314,0.00092926144],"study_design_candidate":"bench_or_experimental","study_design_consensus":"bench_or_experimental","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.000025141706,0.000004563222,0.00031836837,0.0000053820067,0.0000023845914,0.000030611096,0.000007872602,0.00006750752,0.99702424,0.0005724076,0.000035194775,0.0019062548],"study_design_scores_gemma":[0.000011736681,0.000044722135,0.0053607817,0.0000036553934,0.000007400058,0.00026608928,0.000038917122,0.0018356099,0.98938835,0.0004824526,0.0025538774,0.0000063049883],"about_ca_topic_score_codex":0.00034160755,"about_ca_topic_score_gemma":0.001431143,"teacher_disagreement_score":0.0021303701,"about_ca_system_score_codex":0.00043503215,"about_ca_system_score_gemma":0.00028279173,"threshold_uncertainty_score":0.0071267486},"labels":[],"label_agreement":null},{"id":"W2783798065","doi":"10.1038/s41588-018-0086-z","title":"Sequencing of prostate cancers identifies new cancer genes, routes of progression and drug targets","year":2018,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Prostate Cancer Treatment and Research","field":"Medicine","cited_by":238,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Toronto; Ontario Institute for Cancer Research; Princess Margaret Cancer Centre; University Health Network","funders":"National Cancer Institute; National Institute for Health and Care Research; Francis Crick Institute; Cancer Research UK; Wellcome Trust","keywords":"Prostate cancer; Biology; Chromoplexy; Cancer; Disease; Gene; Fusion gene; Mutation; Prostate; Bioinformatics; Genetics; Internal medicine; Medicine; PCA3","score_opus":0.017934515406397566,"score_gpt":0.34798363368850477,"score_spread":0.3300491182821072,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2783798065","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.77839875,0.10280885,0.07633491,0.012985299,0.00054172013,0.0001932388,0.0118314605,0.001184933,0.015720777],"genre_scores_gemma":[0.8915271,0.047209546,0.046030223,0.0027217562,0.0002939362,0.00008348804,0.0054245116,0.00033732268,0.0063720397],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9997334,0.00005230717,0.000017268792,0.00006721538,0.00009784976,0.000031899013],"domain_scores_gemma":[0.99927884,0.00035230673,0.00013877395,0.000049413564,0.00010344698,0.00007723933],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0006558173,0.00040544447,0.00075413426,0.0010239419,0.00029629562,0.0014326232,0.0004181815,0.0007960644,0.0022230842],"category_scores_gemma":[0.0012068741,0.0004051151,0.0007966062,0.0008713848,0.00041421762,0.00062886195,0.00030653254,0.0013375583,0.00062465033],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0018575174,0.0002227377,0.11254317,0.0016879976,0.0006027929,0.0028920388,0.0005155288,0.008672907,0.48864967,0.013098363,0.008329342,0.36092788],"study_design_scores_gemma":[0.00046412033,0.002273783,0.33015922,0.000808647,0.0021969464,0.017351087,0.001074741,0.023869142,0.33788428,0.051886566,0.23180892,0.00022258906],"about_ca_topic_score_codex":0.0019834682,"about_ca_topic_score_gemma":0.004427091,"teacher_disagreement_score":0.0022230842,"about_ca_system_score_codex":0.00073939783,"about_ca_system_score_gemma":0.00091772084,"threshold_uncertainty_score":0.007436931},"labels":[],"label_agreement":null},{"id":"W2788939605","doi":"10.1038/s41588-018-0056-5","title":"Meta-analysis of genome-wide association studies for cattle stature identifies common genes that regulate body size in mammals","year":2018,"lang":"en","type":"review","venue":"Nature Genetics","topic":"Genetic and phenotypic traits in livestock","field":"Biochemistry, Genetics and Molecular Biology","cited_by":467,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Alberta Livestock and Meat Agency; Canadian Natural Resources; University of Alberta; University of Guelph","funders":"","keywords":"Biology; Genome-wide association study; Genetics; Genetic association; Genome; Gene; Meta-analysis; Evolutionary biology; Single-nucleotide polymorphism; Genotype; Internal medicine","score_opus":0.06632364195673797,"score_gpt":0.35642946090880157,"score_spread":0.2901058189520636,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2788939605","genre_codex":"review","genre_gemma":"review","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"review","genre_consensus":"review","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.0004476151,0.998486,0.00023719747,0.00039704354,0.00010699141,0.000003035816,0.00012456969,0.0000060362495,0.00019149228],"genre_scores_gemma":[0.0040797335,0.993958,0.00068970665,0.00058007636,0.00025358493,0.0000080022555,0.00023352409,0.000004090037,0.00019324097],"study_design_codex":"design_other","study_design_gemma":"meta_analysis","domain_scores_codex":[0.9993772,0.00013614306,0.000115015515,0.00020465911,0.00012555502,0.000041553652],"domain_scores_gemma":[0.996136,0.0029330684,0.00040110713,0.00010871269,0.0003065898,0.00011442077],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0030456132,0.0010184078,0.0027615288,0.0024541775,0.00020728436,0.0012154458,0.0014433917,0.0011670914,0.0026648156],"category_scores_gemma":[0.0047242935,0.0003362909,0.0016078462,0.003042155,0.0005311812,0.00075975165,0.0009377805,0.0011744172,0.00044834532],"study_design_candidate":"meta_analysis","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0005883039,0.000043751585,0.009492621,0.05084609,0.008721197,0.0005110308,0.00014114755,0.0005525774,0.00164069,0.0026037416,0.014747206,0.91011184],"study_design_scores_gemma":[0.00031399517,0.00045831501,0.08855367,0.053546187,0.04111798,0.004914593,0.00046765187,0.0004948851,0.0013880541,0.013038008,0.79548264,0.00022393074],"about_ca_topic_score_codex":0.0024393816,"about_ca_topic_score_gemma":0.005387633,"teacher_disagreement_score":0.0030456132,"about_ca_system_score_codex":0.00055031094,"about_ca_system_score_gemma":0.0021869608,"threshold_uncertainty_score":0.016106963},"labels":[],"label_agreement":null},{"id":"W2791237799","doi":"10.1038/s41588-018-0063-6","title":"Human TGF-β1 deficiency causes severe inflammatory bowel disease and encephalopathy","year":2018,"lang":"en","type":"letter","venue":"Nature Genetics","topic":"Pancreatic and Hepatic Oncology Research","field":"Medicine","cited_by":126,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"SickKids Foundation; Hospital for Sick Children; University of Toronto","funders":"National Institute of Diabetes and Digestive and Kidney Diseases; Crohn's and Colitis Foundation","keywords":"Biology; Transforming growth factor; Inflammatory bowel disease; Immunology; Transforming growth factor beta; Loss function; Disease; Genetics; Gene; Phenotype; Endocrinology; Internal medicine; Medicine","score_opus":0.016872484345596808,"score_gpt":0.3182468599701179,"score_spread":0.30137437562452113,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2791237799","genre_codex":"commentary","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":null,"domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.058103926,0.006823963,0.0012130952,0.8870143,0.02399058,0.000056384684,0.00023447978,0.00020053843,0.022362726],"genre_scores_gemma":[0.5567707,0.009242076,0.002434475,0.33595937,0.07273193,0.00007797906,0.00019138888,0.00011084548,0.022481112],"study_design_codex":"case_report","study_design_gemma":"observational","domain_scores_codex":[0.9994679,0.0001841064,0.00006584178,0.00006426076,0.000106324005,0.00011153249],"domain_scores_gemma":[0.9975884,0.0015159927,0.00024086317,0.000104489925,0.00018233675,0.00036797574],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00059800583,0.00062590896,0.00072210556,0.00041755097,0.0009640386,0.00082068995,0.0005167343,0.010685145,0.0025007806],"category_scores_gemma":[0.006910635,0.00032091173,0.00064758986,0.00030862482,0.0010523264,0.00085195963,0.00056178466,0.0058833994,0.0011058715],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00067043275,0.00014202858,0.007690139,0.00015256504,0.00010176476,0.74410534,0.00030574834,0.00030427272,0.003508397,0.0066289124,0.21274006,0.023650343],"study_design_scores_gemma":[0.000973068,0.0006944958,0.012299544,0.00050007296,0.00029055332,0.6680727,0.00068887987,0.0023543409,0.0042296858,0.017796883,0.29198682,0.00011296331],"about_ca_topic_score_codex":0.00085656805,"about_ca_topic_score_gemma":0.0010792351,"teacher_disagreement_score":0.010685145,"about_ca_system_score_codex":0.0013292339,"about_ca_system_score_gemma":0.0005275342,"threshold_uncertainty_score":0.00964427},"labels":[],"label_agreement":null},{"id":"W2791863121","doi":"10.1038/s41588-018-0058-3","title":"Multiancestry genome-wide association study of 520,000 subjects identifies 32 loci associated with stroke and stroke subtypes","year":2018,"lang":"en","type":"review","venue":"Nature Genetics","topic":"Genetic Associations and Epidemiology","field":"Biochemistry, Genetics and Molecular Biology","cited_by":1726,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"McGill University; University of British Columbia; McMaster University; Population Health Research Institute","funders":"National Institute of Diabetes and Digestive and Kidney Diseases; National Heart, Lung, and Blood Institute; National Institute on Aging; Medical Research Council; Novo Nordisk Fonden; National Center for Advancing Translational Sciences; Agence Nationale de la Recherche; National Institute of Neurological Disorders and Stroke; National Institute of General Medical Sciences; National Institute for Health and Care Research; British Heart Foundation; St. Jude Medical; Bayer HealthCare; Broad Institute; Quest Diagnostics; National Institutes of Health; Yale University","keywords":"Genome-wide association study; Biology; Pleiotropy; Linkage disequilibrium; Genetic association; Stroke (engine); Genetics; Etiology; Bioinformatics; Gene; Allele; Internal medicine; Single-nucleotide polymorphism; Haplotype; Phenotype; Medicine; Genotype","score_opus":0.016371797932017654,"score_gpt":0.29392549318222666,"score_spread":0.277553695250209,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2791863121","genre_codex":"review","genre_gemma":"review","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"review","genre_consensus":"review","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.00029885728,0.99739325,0.0003894958,0.00092908187,0.00027285324,0.000005529841,0.00014250174,0.0000136767285,0.00055465155],"genre_scores_gemma":[0.001957691,0.9957254,0.00054486183,0.00069413555,0.00045146214,0.000010482412,0.00020065307,0.0000040459613,0.00041127228],"study_design_codex":"design_other","study_design_gemma":"meta_analysis","domain_scores_codex":[0.9995747,0.00009434062,0.0000767147,0.00011091411,0.000111151196,0.00003205318],"domain_scores_gemma":[0.9980861,0.0012330094,0.00018725714,0.00006826233,0.00033382833,0.000091571],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0020208403,0.001062443,0.0020825218,0.0019473324,0.00020293123,0.00090983283,0.001297114,0.0013262768,0.0020320844],"category_scores_gemma":[0.0025646372,0.00032317758,0.00084093586,0.0022136834,0.00046246292,0.000747465,0.0008653657,0.0017074334,0.000902746],"study_design_candidate":"meta_analysis","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00029602647,0.000044346056,0.0041807443,0.011988993,0.0010063119,0.00028658344,0.000058237452,0.00022891587,0.00061361014,0.00235119,0.031117506,0.9478275],"study_design_scores_gemma":[0.0001830999,0.00021835687,0.024598897,0.012618306,0.0031364772,0.0026037458,0.00016081642,0.00021385183,0.0006461388,0.008260235,0.94725937,0.00010061015],"about_ca_topic_score_codex":0.0021276423,"about_ca_topic_score_gemma":0.0044179694,"teacher_disagreement_score":0.0021276423,"about_ca_system_score_codex":0.00047489547,"about_ca_system_score_gemma":0.0017638215,"threshold_uncertainty_score":0.010687351},"labels":[],"label_agreement":null},{"id":"W2794153231","doi":"10.1038/s41588-018-0050-y","title":"Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity","year":2018,"lang":"en","type":"erratum","venue":"Nature Genetics","topic":"Nutrition, Genetics, and Disease","field":"Biochemistry, Genetics and Molecular Biology","cited_by":15,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"York University; Université de Montréal; Dalhousie University; Montreal Heart Institute","funders":"European Hematology Association; National Institute for Health and Care Research; British Heart Foundation; Cancer Research UK; Medical Research Council; Steno Diabetes Center Copenhagen","keywords":"Biology; Body mass index; Energy expenditure; Obesity; Index (typography); Computational biology; Control (management); Genetics; Bioinformatics; Endocrinology; Computer science; Artificial intelligence; World Wide Web","score_opus":0.006113469550931623,"score_gpt":0.21110264535305026,"score_spread":0.20498917580211864,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2794153231","genre_codex":"editorial","genre_gemma":"other","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"other","genre_consensus":null,"domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.00014492088,0.00072269,0.00049324956,0.027046192,0.96831536,0.000013221844,0.0007292179,0.00021749163,0.002317696],"genre_scores_gemma":[0.019239474,0.0082473755,0.0075485203,0.07455073,0.43231463,0.00022149507,0.004119694,0.002670891,0.45108727],"study_design_codex":"not_applicable","study_design_gemma":"not_applicable","domain_scores_codex":[0.997232,0.00040814895,0.0005248489,0.00041921053,0.0011503957,0.0002654035],"domain_scores_gemma":[0.97775877,0.0053785886,0.0010704105,0.001465646,0.013381491,0.00094497274],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0030503483,0.0019209023,0.0017758801,0.0034808333,0.002751113,0.003598836,0.003352032,0.005623579,0.065396495],"category_scores_gemma":[0.042422924,0.0011472552,0.0016094967,0.0018059262,0.0017100711,0.001815032,0.0014668376,0.0103227245,0.030746726],"study_design_candidate":"not_applicable","study_design_consensus":"not_applicable","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00003513307,0.000005615022,0.00009626833,0.00009243196,0.000015103659,0.00049195177,0.000020618596,0.000043646112,0.00004682308,0.00056031474,0.99284464,0.005747502],"study_design_scores_gemma":[0.000058170193,0.000019662315,0.0009941934,0.00038082586,0.00006525236,0.0013892971,0.000067080924,0.0002599212,0.00042655435,0.0015456417,0.99475217,0.000041165255],"about_ca_topic_score_codex":0.013840727,"about_ca_topic_score_gemma":0.021568153,"teacher_disagreement_score":0.065396495,"about_ca_system_score_codex":0.0030961493,"about_ca_system_score_gemma":0.0036931003,"threshold_uncertainty_score":0.21877307},"labels":[],"label_agreement":null},{"id":"W2802815532","doi":"10.1038/s41588-018-0269-7","title":"Discovery of the first genome-wide significant risk loci for attention deficit/hyperactivity disorder","year":2018,"lang":"en","type":"review","venue":"Nature Genetics","topic":"Attention Deficit Hyperactivity Disorder","field":"Medicine","cited_by":2320,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"SickKids Foundation; Hospital for Sick Children; University of Toronto","funders":"Cilag; National Institute of Diabetes and Digestive and Kidney Diseases; Seventh Framework Programme; Agència de Gestió d'Ajuts Universitaris i de Recerca; National Health and Medical Research Council; Medical Research Council; Canadian Institutes of Health Research; National Institutes of Health; Servier; Novo Nordisk Fonden; Norges Forskningsråd; National Institute of Mental Health; Horizon 2020 Framework Programme; Aarhus Universitet; QIMR Berghofer Medical Research Institute; KU Leuven; Eli Lilly and Company; Lundbeckfonden; Ministerio de Economía y Competitividad; Deutsche Forschungsgemeinschaft; King's College London; European College of Neuropsychopharmacology; Alzheimer's Association; American Society of Clinical Psychopharmacology; Nederlandse Organisatie voor Wetenschappelijk Onderzoek; Wellcome Trust; H. Lundbeck A/S; Sunovion; Universitetet i Bergen; Novo Nordisk; Generalitat de Catalunya; National Institute for Health and Care Research; Massachusetts General Hospital; Broad Institute; Indivior; Pfizer; Action Medical Research; U.S. Department of Veterans Affairs","keywords":"Biology; Attention deficit hyperactivity disorder; Genome-wide association study; Genome; Genetics; Computational biology; Gene; Psychiatry; Single-nucleotide polymorphism; Genotype; Psychology","score_opus":0.03040067920894911,"score_gpt":0.3274078234753422,"score_spread":0.2970071442663931,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2802815532","genre_codex":"review","genre_gemma":"review","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"review","genre_consensus":"review","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.000116396885,0.9989166,0.0000760879,0.0003722992,0.00010185921,0.0000027660144,0.00002584648,0.0000047016283,0.00038351328],"genre_scores_gemma":[0.001024579,0.9982439,0.00014025366,0.00024349814,0.000105296385,0.000003747341,0.000045853805,0.0000016247518,0.00019124532],"study_design_codex":"design_other","study_design_gemma":"systematic_review","domain_scores_codex":[0.999701,0.00006252687,0.000059503996,0.000063919804,0.000088815985,0.000024304756],"domain_scores_gemma":[0.9991359,0.00048795005,0.000109646346,0.000024044793,0.00018361851,0.00005875756],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0009868094,0.00061790814,0.0013674482,0.002476599,0.00021181467,0.0007576798,0.00092060346,0.0010612498,0.0030414995],"category_scores_gemma":[0.0020615906,0.00026353262,0.00073130574,0.002280145,0.00046474944,0.00076961156,0.0007336323,0.0014448927,0.0012689335],"study_design_candidate":"systematic_review","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00013939138,0.0000253508,0.00087854755,0.029706022,0.0005221836,0.0003471482,0.00007461895,0.00019978934,0.0007230741,0.0027416062,0.024836108,0.9398061],"study_design_scores_gemma":[0.00005896592,0.00010233513,0.0054557063,0.015251585,0.0013525996,0.002907327,0.00009629746,0.0000905501,0.0005334865,0.003177374,0.970933,0.00004065369],"about_ca_topic_score_codex":0.0015936762,"about_ca_topic_score_gemma":0.0024153097,"teacher_disagreement_score":0.0030414995,"about_ca_system_score_codex":0.00063863856,"about_ca_system_score_gemma":0.0019260332,"threshold_uncertainty_score":0.0101748705},"labels":[],"label_agreement":null},{"id":"W2803499181","doi":"10.1038/s41588-018-0120-1","title":"Analysis of the androgen receptor–regulated lncRNA landscape identifies a role for ARLNC1 in prostate cancer progression","year":2018,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Cancer-related molecular mechanisms research","field":"Biochemistry, Genetics and Molecular Biology","cited_by":238,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Simon Fraser University","funders":"National Institute of General Medical Sciences; National Cancer Institute; National Institutes of Health","keywords":"Prostate cancer; Androgen receptor; Gene knockdown; Biology; Long non-coding RNA; Cancer research; Transcriptome; Prostate; Signal transduction; Cancer; Androgen; RNA; Endocrinology; Cell biology; Gene expression; Cell culture; Gene; Genetics; Hormone","score_opus":0.005267101809455372,"score_gpt":0.30045347232883207,"score_spread":0.2951863705193767,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2803499181","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.98039514,0.0043951687,0.0071645468,0.00052065204,0.000057419056,0.000018771827,0.001977613,0.00028996746,0.005180723],"genre_scores_gemma":[0.9939069,0.00073789456,0.0019258172,0.00015148275,0.000012893026,0.000011244146,0.00078851345,0.000053775784,0.002411442],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99983907,0.000011738156,0.0000062044087,0.00005794382,0.00005147569,0.000033563687],"domain_scores_gemma":[0.9998658,0.000027894808,0.000037879312,0.000013960758,0.00002672205,0.00002775814],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00017046886,0.0001547315,0.00019451004,0.0006054519,0.00036761144,0.0007037209,0.0002299531,0.00021368066,0.0029284537],"category_scores_gemma":[0.00021938201,0.00017810497,0.0002967734,0.0004943699,0.00029676463,0.00029431668,0.0002588133,0.00044821153,0.00047766347],"study_design_candidate":"bench_or_experimental","study_design_consensus":"bench_or_experimental","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00019066581,0.000017778035,0.009594743,0.00007549149,0.000034103192,0.00012514344,0.000044510554,0.0005260337,0.97897524,0.0009478661,0.00033115613,0.009137269],"study_design_scores_gemma":[0.00003655436,0.0003293352,0.34509766,0.000038166894,0.00018950134,0.0018303441,0.00041180526,0.014001899,0.6125092,0.003121104,0.022357758,0.000076691664],"about_ca_topic_score_codex":0.0025369737,"about_ca_topic_score_gemma":0.006883028,"teacher_disagreement_score":0.0029284537,"about_ca_system_score_codex":0.0005711752,"about_ca_system_score_gemma":0.00039652528,"threshold_uncertainty_score":0.009796679},"labels":[],"label_agreement":null},{"id":"W2804575948","doi":"10.1038/s41588-018-0127-7","title":"Genome-wide association meta-analysis highlights light-induced signaling as a driver for refractive error","year":2018,"lang":"en","type":"review","venue":"Nature Genetics","topic":"Ophthalmology and Visual Impairment Studies","field":"Medicine","cited_by":378,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"SickKids Foundation; Hospital for Sick Children; University of Toronto","funders":"National Heart, Lung, and Blood Institute; National Medical Research Council; National Health and Medical Research Council; Alcon Research Institute; Stichting Nederlands Oogheelkundig Onderzoek; Abbott Diabetes Care; National Institutes of Health; Westmead Millennium Institute for Medical Research; Moorfields Eye Charity; Medical Research Council; Tartu Ülikool; State Government of Victoria; Diabetes UK; Ohio Lions Eye Research Foundation; Algemene Nederlandse Vereniging ter voorkoming van Blindheid; Tampereen Yliopisto; Erasmus Medisch Centrum; Vrije Universiteit Amsterdam; ZonMw; Moorfields Eye Hospital NHS Foundation Trust; Macula Society; Northwest Regional Development Agency; Nederlandse Organisatie voor Wetenschappelijk Onderzoek; Flinders University; European Commission; European Regional Development Fund; King's College London; Singapore Eye Research Institute; Jyväskylän Yliopisto; Wellcome Trust; National University of Singapore; Landelijke Stichting voor Blinden en Slechtzienden; Cancer Research UK; Turun Yliopistollinen Keskussairaala; Stichting Steunfonds Uitzicht; Pfizer Australia; Horizon 2020 Framework Programme; Turun Yliopisto; Hrvatska Zaklada za Znanost; Scottish Government; QIMR Berghofer Medical Research Institute; Bundesministerium für Bildung und Forschung; British Heart Foundation; Case Western Reserve University; National Eye Institute; National Institute for Health and Care Research; Pfizer; International Glaucoma Association; Institute of Genetics; Agence Nationale de la Recherche; Biomedical Research Council; Ophthalmic Research Institute of Australia; Oogfonds; European Foundation for the Study of Diabetes; American Health Assistance Foundation; Research to Prevent Blindness","keywords":"Biology; Retina; Retinal pigment epithelium; Genetic association; Genome-wide association study; Retinal; Extracellular matrix; Genetics; Blindness; Refractive error; Cell biology; Neuroscience; Computational biology; Gene; Single-nucleotide polymorphism; Genotype; Eye disease; Optometry; Medicine","score_opus":0.11167872548187605,"score_gpt":0.4318228611241954,"score_spread":0.32014413564231936,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2804575948","genre_codex":"review","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":null,"domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.011322879,0.98487824,0.0007576541,0.0012253067,0.0003024749,0.00001326041,0.0008149558,0.000018078032,0.000667225],"genre_scores_gemma":[0.2818563,0.70959127,0.0021730186,0.002698055,0.00083747646,0.00005339011,0.0018546662,0.000031795826,0.0009040046],"study_design_codex":"meta_analysis","study_design_gemma":"meta_analysis","domain_scores_codex":[0.9983596,0.0005576277,0.00035565146,0.00041316357,0.00020589947,0.000108062515],"domain_scores_gemma":[0.994073,0.004816002,0.000521814,0.00022341056,0.0002767385,0.000089148736],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0028427206,0.0011499138,0.0026140942,0.0012572579,0.00027490171,0.0015106717,0.001180733,0.0015168628,0.004086383],"category_scores_gemma":[0.0092702685,0.0004154819,0.008113711,0.0025748634,0.000313696,0.00080154225,0.00078425405,0.0015411027,0.0003003631],"study_design_candidate":"meta_analysis","study_design_consensus":"meta_analysis","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.005064749,0.000127056,0.17877305,0.104947925,0.40453,0.0019451306,0.00041453695,0.0015908672,0.0025109716,0.0035001952,0.01421361,0.28238198],"study_design_scores_gemma":[0.0007295986,0.00046708717,0.17073938,0.016191142,0.7560059,0.001890274,0.0003980701,0.00071201887,0.0010019962,0.0070196744,0.04472379,0.00012103621],"about_ca_topic_score_codex":0.005373096,"about_ca_topic_score_gemma":0.009995987,"teacher_disagreement_score":0.005373096,"about_ca_system_score_codex":0.0004461565,"about_ca_system_score_gemma":0.0012731283,"threshold_uncertainty_score":0.01503396},"labels":[],"label_agreement":null},{"id":"W2806504012","doi":"10.1038/s41588-018-0142-8","title":"Association analyses of more than 140,000 men identify 63 new prostate cancer susceptibility loci","year":2018,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Genetic Associations and Epidemiology","field":"Biochemistry, Genetics and Molecular Biology","cited_by":1010,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Alberta; Princess Margaret Cancer Centre","funders":"Servicio Gallego de Salud; Cancer Council Queensland; Cancer Council Victoria; Medical Research Council; Canadian Institutes of Health Research; National Institutes of Health; Warwick Medical School; Turun Yliopistollinen Keskussairaala; Division of Cancer Epidemiology and Genetics, National Cancer Institute; Tampereen Yliopisto; National Heart, Lung, and Blood Institute; Peter MacCallum Cancer Centre; Karolinska Institutet; DOD Prostate Cancer Research Program; Cambridge University Hospitals; Queensland University of Technology; Griffith University; National Cancer Institute; University of Bristol; Monash Biomedicine Discovery Institute, Monash University; University of Oxford; University of Warwick; Harvard T.H. Chan School of Public Health; Aarhus Universitetshospital; National Institute for Health and Care Research; Breast Cancer Research Foundation; University of Cambridge; University College London; University of Southern California; Cancer Research UK; Monash University; Australian Prostate Cancer Research; Tays; Institut for Klinisk Medicin, Aarhus Universitet; Prostate Cancer Foundation of Australia; Ovarian Cancer Research Fund; Case Western Reserve University; Royal Marsden NHS Foundation Trust; National Cancer Research Institute; Uppsala Universitet; Prostate Cancer Foundation; European Commission; U.S. Department of Defense; Turun Yliopisto; Aarhus Universitet; National Health and Medical Research Council; Cancer Research Institute","keywords":"Biology; Prostate cancer; Genetics; Cancer; Genome-wide association study; Single-nucleotide polymorphism; Genotype; Gene","score_opus":0.018401182870263176,"score_gpt":0.36118729458838056,"score_spread":0.3427861117181174,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2806504012","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9916169,0.0036373208,0.0012813323,0.00029477038,0.000044645225,0.000016744163,0.0018204242,0.00006200315,0.0012257977],"genre_scores_gemma":[0.996075,0.0008287561,0.00087537593,0.00014023282,0.00004946244,0.000015549227,0.0012592489,0.000024870398,0.0007314674],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9986249,0.00032012266,0.00012024159,0.00041706342,0.00035723572,0.0001604597],"domain_scores_gemma":[0.99640214,0.0015960656,0.0008733628,0.00047440844,0.00028819722,0.0003657971],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0017994075,0.0005243564,0.0007703629,0.0011811345,0.00079070154,0.00092661916,0.000600839,0.00071470544,0.0023631384],"category_scores_gemma":[0.004738642,0.0005158586,0.0011405895,0.003753022,0.000557031,0.00042248634,0.00069131283,0.00086301635,0.00048945664],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00040178775,0.000058410813,0.98788154,0.00004197451,0.0006475818,0.00022158546,0.0001197429,0.000092350914,0.0024147325,0.00009411393,0.0005503484,0.0074759102],"study_design_scores_gemma":[0.0000290324,0.00006911308,0.9973502,0.000006423946,0.00030071932,0.00042802747,0.000058926766,0.00012393083,0.00038593684,0.00014120611,0.0010989202,0.0000073851147],"about_ca_topic_score_codex":0.00514886,"about_ca_topic_score_gemma":0.008646797,"teacher_disagreement_score":0.00514886,"about_ca_system_score_codex":0.0002474055,"about_ca_system_score_gemma":0.0005859997,"threshold_uncertainty_score":0.010237753},"labels":[],"label_agreement":null},{"id":"W2807295499","doi":"10.1038/s41588-018-0133-9","title":"Multi-ethnic genome-wide association study for atrial fibrillation","year":2018,"lang":"en","type":"review","venue":"Nature Genetics","topic":"Genetic Associations and Epidemiology","field":"Biochemistry, Genetics and Molecular Biology","cited_by":810,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Hamilton Health Sciences; University of Alberta; McMaster University; Population Health Research Institute","funders":"National Institute of General Medical Sciences; National Human Genome Research Institute; National Heart, Lung, and Blood Institute; Medical Research Council; Biosense Webster; National Institutes of Health; Doris Duke Charitable Foundation; Novo Nordisk Fonden; Yale University; Fondation Leducq; Broad Institute; European Commission; Quest Diagnostics; Amarin Corporation; Bristol-Myers Squibb; St. Jude Medical; Regeneron Pharmaceuticals; British Heart Foundation","keywords":"Biology; Genome-wide association study; Atrial fibrillation; Ethnic group; Genetics; Genetic association; Association (psychology); Computational biology; Evolutionary biology; Internal medicine; Gene; Single-nucleotide polymorphism; Genotype; Anthropology; Medicine","score_opus":0.04551355418812808,"score_gpt":0.3765784192778404,"score_spread":0.33106486508971233,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2807295499","genre_codex":"review","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":null,"domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.00015102657,0.9979032,0.00018023839,0.0007129332,0.00031319796,0.0000067521205,0.00005671437,0.000008572875,0.0006673186],"genre_scores_gemma":[0.0017467269,0.9965654,0.00024101969,0.00048650274,0.00039562563,0.000015512334,0.00011780184,0.0000031660536,0.00042815326],"study_design_codex":"design_other","study_design_gemma":"observational","domain_scores_codex":[0.9994462,0.00012641701,0.00008688937,0.00012271889,0.00017464842,0.000043128613],"domain_scores_gemma":[0.99876887,0.0006132017,0.000194542,0.000041649884,0.00026627965,0.00011545967],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0013290073,0.0010027479,0.0019662075,0.0021270753,0.00025330004,0.00064079865,0.0010157814,0.0015684068,0.004303603],"category_scores_gemma":[0.0020628937,0.00024322009,0.00082887884,0.0025323865,0.00047325733,0.00058032345,0.00064965704,0.0017831569,0.0020173918],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0001815759,0.000051390896,0.0029368098,0.009625774,0.000738698,0.0002538219,0.00004138663,0.00015773858,0.00041785225,0.0021012614,0.040805306,0.9426884],"study_design_scores_gemma":[0.00017715996,0.00024043761,0.028663386,0.013573601,0.0021898618,0.00520299,0.00008526859,0.00023808694,0.00054025406,0.0050221225,0.94398326,0.000083583145],"about_ca_topic_score_codex":0.00145657,"about_ca_topic_score_gemma":0.0022938596,"teacher_disagreement_score":0.004303603,"about_ca_system_score_codex":0.00048895535,"about_ca_system_score_gemma":0.0011487396,"threshold_uncertainty_score":0.0143969655},"labels":[],"label_agreement":null},{"id":"W2807921964","doi":"10.1038/s41588-018-0132-x","title":"A transcriptome-wide association study of 229,000 women identifies new candidate susceptibility genes for breast cancer","year":2018,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Molecular Biology Techniques and Applications","field":"Biochemistry, Genetics and Molecular Biology","cited_by":246,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"McGill University and Génome Québec Innovation Centre; University of British Columbia; McGill University; Université Laval; Queen's University; BC Cancer Agency; Royal Victoria Hospital; Centre hospitalier universitaire de Québec; Mount Sinai Hospital; Lunenfeld-Tanenbaum Research Institute; University Health Network; University of Toronto","funders":"National Cancer Institute; Canadian Institutes of Health Research; Medical Research Council; Ministero dello Sviluppo Economico; National Institutes of Health; Vanderbilt University Medical Center; Cancer Research UK; Government of Canada; Fondation du cancer du sein du Québec; Vanderbilt University; Ministère du Développement Économique, de l’Innovation et de l’Exportation; National Institute for Health and Care Research; Genome Canada; European Commission","keywords":"Biology; Transcriptome; Breast cancer; Candidate gene; Genetics; Gene; Computational biology; Cancer; Bioinformatics; Gene expression","score_opus":0.0068004432755244225,"score_gpt":0.2947232732453293,"score_spread":0.2879228299698049,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2807921964","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9975096,0.00039021493,0.00026834328,0.000089658584,0.000007803179,0.0000056068848,0.0013848762,0.000009253055,0.00033456014],"genre_scores_gemma":[0.9969699,0.00024691102,0.00029841607,0.000079737874,0.000011295675,0.000010974947,0.0018980587,0.000007880322,0.0004769881],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99961746,0.000097632146,0.000026236568,0.00013714295,0.000058363235,0.00006318285],"domain_scores_gemma":[0.99954873,0.00017676436,0.0000841506,0.0000735735,0.000048292433,0.00006846558],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00043962518,0.00020880882,0.00047119928,0.0005546663,0.00061806804,0.00050255633,0.00024274632,0.00034362433,0.0010850913],"category_scores_gemma":[0.0012368844,0.00028804017,0.00037158641,0.0012996268,0.00025117482,0.0001746319,0.00035987727,0.00034982176,0.00025597567],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00056152337,0.000050684528,0.97365326,0.000034035806,0.0003685868,0.00044469323,0.00023004106,0.00006169051,0.019159418,0.000049679278,0.0005935822,0.0047928975],"study_design_scores_gemma":[0.00001233569,0.00004276781,0.99833727,0.000002196531,0.0001128399,0.00034588348,0.00011453842,0.00007125233,0.00035577884,0.000030872052,0.00057144795,0.0000028236445],"about_ca_topic_score_codex":0.005365655,"about_ca_topic_score_gemma":0.008504566,"teacher_disagreement_score":0.005365655,"about_ca_system_score_codex":0.00015714888,"about_ca_system_score_gemma":0.0003117209,"threshold_uncertainty_score":0.010668874},"labels":[],"label_agreement":null},{"id":"W2808357284","doi":"10.1038/s41588-018-0138-4","title":"A precision oncology approach to the pharmacological targeting of mechanistic dependencies in neuroendocrine tumors","year":2018,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Neuroendocrine Tumor Research Advances","field":"Medicine","cited_by":226,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Toronto; University Health Network","funders":"National Center for Research Resources; National Institutes of Health; National Cancer Institute; Irving Medical Center, Columbia University; Swedish Cancer Foundation","keywords":"Regulator; Biology; Neuroendocrine tumors; Cancer research; Malignancy; Computational biology; Transcriptome; Precision oncology; Bioinformatics; Precision medicine; Genetics; Gene; Gene expression; Endocrinology","score_opus":0.028904041199826397,"score_gpt":0.37070384929715017,"score_spread":0.3417998080973238,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2808357284","genre_codex":"methods","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":null,"domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.14601755,0.17969292,0.5035604,0.07329828,0.0051212288,0.0006932125,0.0017814378,0.002385585,0.08744931],"genre_scores_gemma":[0.7983757,0.09050878,0.08321282,0.011687758,0.0018373743,0.00039700515,0.0006275765,0.00023878229,0.013114147],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9995235,0.00012069655,0.00002314048,0.00008834164,0.00016992382,0.00007440404],"domain_scores_gemma":[0.9993243,0.00031577432,0.00011387634,0.00011335787,0.000080084734,0.000052653246],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0019825567,0.000575563,0.0008961521,0.0006934627,0.00051188545,0.0021327783,0.0011594031,0.0010751827,0.0051726904],"category_scores_gemma":[0.0015596146,0.0003740717,0.0008819431,0.00036608524,0.001475192,0.0016582427,0.001464571,0.0044903536,0.00075673964],"study_design_candidate":"bench_or_experimental","study_design_consensus":"bench_or_experimental","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0009701304,0.00067934504,0.0025465044,0.0015638763,0.00046977223,0.0010692186,0.0003124631,0.0124523565,0.36226404,0.26517504,0.017241886,0.33525535],"study_design_scores_gemma":[0.0009144621,0.0039279456,0.0057857553,0.0008873124,0.0007900832,0.004821559,0.0004914488,0.019325232,0.21108475,0.29558697,0.45615885,0.00022560952],"about_ca_topic_score_codex":0.0006020995,"about_ca_topic_score_gemma":0.0015095256,"teacher_disagreement_score":0.0051726904,"about_ca_system_score_codex":0.0012560938,"about_ca_system_score_gemma":0.0012897587,"threshold_uncertainty_score":0.01730442},"labels":[],"label_agreement":null},{"id":"W2808765268","doi":"10.1038/s41588-018-0334-2","title":"Protein-coding variants implicate novel genes related to lipid homeostasis contributing to body-fat distribution","year":2019,"lang":"en","type":"review","venue":"Nature Genetics","topic":"Genetic Associations and Epidemiology","field":"Biochemistry, Genetics and Molecular Biology","cited_by":112,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"York University; Université de Montréal; Montreal Heart Institute","funders":"FP7 Ideas: European Research Council; Eunice Kennedy Shriver National Institute of Child Health and Human Development; National Center for Advancing Translational Sciences; National Institute of Diabetes and Digestive and Kidney Diseases; National Institute of General Medical Sciences; Helmholtz Zentrum München; National Human Genome Research Institute; Hrvatska Zaklada za Znanost; National Institute on Drug Abuse; Imperial College Healthcare NHS Trust; NIHR Oxford Biomedical Research Centre; Hjärt-Lungfonden; Medical Research Council; Scottish Funding Council; NIHR Cambridge Biomedical Research Centre; NIHR BioResource; Universiteit Leiden; National Heart, Lung, and Blood Institute; Kaiser Foundation Research Institute; Directorate for Biological Sciences; National Institutes of Health; H. Lundbeck A/S; Fondation Leenaards; Institut de Cardiologie de Montréal; Marcus och Amalia Wallenbergs minnesfond; Government of Western Australia; Paavo Nurmen Säätiö; Tampereen Tuberkuloosisäätiö; National Health and Medical Research Council; Deutsche Krebshilfe; Sydäntutkimussäätiö; Vetenskapsrådet; Novo Nordisk; National Institute for Health Research Health Protection Research Unit; Universitätsklinikum Regensburg; Diabetesliitto; Leids Universitair Medisch Centrum; Steno Diabetes Center Copenhagen; SystemsX.ch; Universitetet i Bergen; Emil Aaltosen Säätiö; Wake Forest School of Medicine; Taichung Veterans General Hospital; Helse Vest; National Cancer Institute; European Regional Development Fund; Max-Planck-Gesellschaft; Region Hovedstaden; Kuopion Yliopistollinen Sairaala; American Heart Association; Suomen Kulttuurirahasto; Turun Yliopistollinen Keskussairaala; European Commission; Knut och Alice Wallenbergs Stiftelse; Tekes; Schweizerischer Nationalfonds zur Förderung der Wissenschaftlichen Forschung; National Medical Research Council; Norges Forskningsråd; Australian Government; QIMR Berghofer Medical Research Institute; Lunds Universitet; Deutsche Forschungsgemeinschaft; Nederlandse Organisatie voor Wetenschappelijk Onderzoek; Ministero della Salute; Eesti Teadusagentuur; Päivikki ja Sakari Sohlbergin Säätiö; Raine Medical Research Foundation; Public Health England; Edith Cowan University; Diabetestutkimussäätiö; Foundation for Cardiovascular Research; ZonMw; Université de Montréal; Kela; National Natural Science Foundation of China; National Science Council; British Heart Foundation; National Institute for Health and Care Research; Johns Hopkins University; Wellcome Trust; Cancer Research UK; Royal Marsden NHS Foundation Trust; Socialdepartementet; School of Medicine, Boston University; European Hematology Association; Li Ka Shing Foundation; University of Notre Dame; Imperial College London; Fondation Institut de Cardiologie de Montréal; NIHR Exeter Clinical Research Facility; Erasmus Medisch Centrum; Lundbeckfonden; Doktor Robert Pfleger-Stiftung; National Science Foundation; Fondation Leducq; Diabetesforbundet; Pfizer; Northwestern University; Horizon 2020 Framework Programme; University of Minnesota; Juho Vainion Säätiö; Novo Nordisk Fonden","keywords":"Biology; Genome-wide association study; Genetics; Gene; Body fat distribution; Minor allele frequency; Adipose tissue; Allele; Allele frequency; Endocrinology; Single-nucleotide polymorphism; Genotype","score_opus":0.02312488381428673,"score_gpt":0.327225867781663,"score_spread":0.3041009839673763,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2808765268","genre_codex":"review","genre_gemma":"review","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"review","genre_consensus":"review","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.0000950273,0.9972445,0.00030244174,0.0011619506,0.0005123465,0.0000029349324,0.000058752805,0.000010499586,0.0006116493],"genre_scores_gemma":[0.0006471261,0.99680233,0.0003867927,0.000706117,0.0008106947,0.0000059329736,0.00008587532,0.00000248249,0.0005526495],"study_design_codex":"design_other","study_design_gemma":"observational","domain_scores_codex":[0.99971575,0.00005464944,0.000047426944,0.000076951,0.00008304136,0.000022152504],"domain_scores_gemma":[0.99888796,0.000720282,0.00010670874,0.000027816232,0.00018941138,0.000067855115],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0010855664,0.0013008076,0.0016934236,0.0018623449,0.0001800996,0.00095059094,0.001203831,0.0016844983,0.0029401626],"category_scores_gemma":[0.0017832011,0.00024889223,0.0005099057,0.0023641966,0.0006835825,0.0008152817,0.0007025556,0.0020289603,0.0014580388],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.000137885,0.00004579512,0.0011753093,0.008860577,0.0003177693,0.00043234823,0.000028827337,0.0003017769,0.0009402635,0.0041825217,0.06846228,0.91511464],"study_design_scores_gemma":[0.00006181046,0.00006391166,0.005086299,0.0061198757,0.00063919195,0.002729817,0.00007495847,0.00016753218,0.00036537315,0.006049272,0.9785963,0.000045606528],"about_ca_topic_score_codex":0.0019988974,"about_ca_topic_score_gemma":0.0032567359,"teacher_disagreement_score":0.0029401626,"about_ca_system_score_codex":0.00068537804,"about_ca_system_score_gemma":0.0012046281,"threshold_uncertainty_score":0.00983578},"labels":[],"label_agreement":null},{"id":"W2809193491","doi":"10.1038/s41588-018-0152-6","title":"Genome-wide association meta-analysis in 269,867 individuals identifies new genetic and functional links to intelligence","year":2018,"lang":"en","type":"review","venue":"Nature Genetics","topic":"Genetic Associations and Epidemiology","field":"Biochemistry, Genetics and Molecular Biology","cited_by":1418,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Toronto; Centre for Addiction and Mental Health","funders":"Jane and Terry Semel Institute for Neuroscience and Human Behavior, University of California, Los Angeles; NIH Clinical Center; National Institute of Dental and Craniofacial Research; National Institute of Neurological Disorders and Stroke; National Institute of Biomedical Imaging and Bioengineering; National Human Genome Research Institute; Syddansk Universitet; National Institute of Mental Health; Institute for Molecular Bioscience, University Of Queensland; University of Galway; Medical Research Council; National Institute on Drug Abuse; Biotechnology and Biological Sciences Research Council; Stanley Center for Psychiatric Research, Broad Institute; Pfizer; University of California, Los Angeles; National Institutes of Health; National Institute on Aging; National University of Ireland; National Institute on Alcohol Abuse and Alcoholism; Centre for Cognitive Ageing and Cognitive Epidemiology; Yale University; Karolinska Institutet; Queensland Brain Institute; H. Lundbeck A/S; Johns Hopkins University; Universitetet i Oslo; Universitetet i Bergen; National Center for Research Resources; National and Kapodistrian University of Athens; University of Crete; Imperial College London; University of Toronto; Schweizerischer Nationalfonds zur Förderung der Wissenschaftlichen Forschung; Broad Institute; Directorate for Biological Sciences; Northwell Health; Trinity College Dublin; Erasmus Universitair Medisch Centrum Rotterdam; University of Oregon; King's College London; Virginia Commonwealth University; Helsingin Yliopisto; Haukeland Universitetssjukehus; Nederlandse Organisatie voor Wetenschappelijk Onderzoek; Wellcome Trust; University of Southern California; National Science Foundation; University of Minnesota; Massachusetts General Hospital; Department of Psychology and Neuroscience, Duke University; Eli Lilly and Company; University of North Carolina at Chapel Hill; Brigham and Women's Hospital","keywords":"Biology; Genome-wide association study; Computational biology; Genetic association; Genetics; Meta-analysis; Association (psychology); Genome; Single-nucleotide polymorphism; Gene; Genotype","score_opus":0.054488888012075555,"score_gpt":0.34061248458524435,"score_spread":0.28612359657316877,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2809193491","genre_codex":"review","genre_gemma":"review","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"review","genre_consensus":"review","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.0029388778,0.9936287,0.00086280983,0.0011655985,0.00026787753,0.000009218557,0.00047516968,0.000018440853,0.00063325785],"genre_scores_gemma":[0.027831277,0.9673734,0.0017524151,0.0011096733,0.00060817436,0.00002608889,0.0009045957,0.000010076943,0.0003843575],"study_design_codex":"design_other","study_design_gemma":"meta_analysis","domain_scores_codex":[0.9991897,0.00022999258,0.00015660636,0.00022181352,0.0001547355,0.000047106812],"domain_scores_gemma":[0.9969007,0.0023566498,0.000294355,0.00012263711,0.00024706795,0.00007863024],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0030516002,0.0011614972,0.0020785904,0.001979308,0.00020575673,0.0010161855,0.0011737507,0.0012376291,0.0018101955],"category_scores_gemma":[0.005224897,0.00040367353,0.0020853302,0.0030453005,0.00042341126,0.0006387432,0.00086278823,0.0013960501,0.00035675682],"study_design_candidate":"meta_analysis","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0013851067,0.00009133966,0.067444645,0.03575041,0.02978598,0.0012150255,0.00020117455,0.00093219854,0.0014975131,0.0036783968,0.025268981,0.83274925],"study_design_scores_gemma":[0.0009156723,0.00066088705,0.30034265,0.030259022,0.12928902,0.00834722,0.00057707063,0.00095930154,0.0023170274,0.027185887,0.49879888,0.00034740052],"about_ca_topic_score_codex":0.0029124636,"about_ca_topic_score_gemma":0.0067612734,"teacher_disagreement_score":0.0030516002,"about_ca_system_score_codex":0.00039577414,"about_ca_system_score_gemma":0.0014854472,"threshold_uncertainty_score":0.016138554},"labels":[],"label_agreement":null},{"id":"W2883063010","doi":"10.1038/s41588-018-0168-y","title":"Common variation near IRF6 is associated with IFN-β-induced liver injury in multiple sclerosis","year":2018,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Hepatitis B Virus Studies","field":"Medicine","cited_by":40,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"London Health Sciences Centre; Western University; University of Manitoba; Université de Montréal; University of Alberta; Dalhousie University; BC Children's Hospital; University of British Columbia","funders":"National Institute of Neurological Disorders and Stroke; National Institute of Diabetes and Digestive and Kidney Diseases; National Center for Research Resources; National Institute of General Medical Sciences; Wellcome Trust","keywords":"Multiple sclerosis; Liver injury; Odds ratio; Biology; Liver disease; IRF1; Internal medicine; Immunology; Medicine; Endocrinology; Gene; Genetics; Gene expression","score_opus":0.035593153436061134,"score_gpt":0.2760924274739879,"score_spread":0.24049927403792676,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2883063010","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99858344,0.00025474434,0.0004990717,0.0000727581,0.000016915157,0.00000366905,0.00017692977,0.000014004274,0.00037848126],"genre_scores_gemma":[0.9991479,0.000060169117,0.0003155542,0.000045305773,0.000015340658,0.0000028503514,0.0001268074,0.000014897134,0.0002710663],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9990711,0.00031439934,0.00013155352,0.00027167096,0.0001119787,0.00009925609],"domain_scores_gemma":[0.99831724,0.0005545838,0.0006378723,0.00016355941,0.000111573994,0.00021508973],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0006246319,0.0005538595,0.00047836406,0.0014486181,0.000609736,0.00048506726,0.00046943536,0.0009035566,0.004578],"category_scores_gemma":[0.001491192,0.00023182739,0.001104048,0.00121066,0.0004440922,0.00028019174,0.0004554487,0.0008751212,0.00037002712],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.007410283,0.00036081285,0.57756996,0.00021206017,0.0025669648,0.0057963994,0.0013835924,0.00052727485,0.3838325,0.0008292355,0.00058821903,0.018922694],"study_design_scores_gemma":[0.00008552373,0.00056340627,0.983192,0.000051399285,0.0004975961,0.0056554587,0.0003337787,0.0006149879,0.007493545,0.0006115525,0.00087131315,0.000029408822],"about_ca_topic_score_codex":0.00151959,"about_ca_topic_score_gemma":0.0016466171,"teacher_disagreement_score":0.004578,"about_ca_system_score_codex":0.00016682656,"about_ca_system_score_gemma":0.00014182024,"threshold_uncertainty_score":0.015314937},"labels":[],"label_agreement":null},{"id":"W2883211905","doi":"10.1038/s41588-018-0173-1","title":"Type 2 diabetes risk alleles in PAM impact insulin release from human pancreatic β-cells","year":2018,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Pancreatic function and diabetes","field":"Medicine","cited_by":86,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Alberta","funders":"National Institute of Diabetes and Digestive and Kidney Diseases; University of Oxford; Medical Research Council; Diabetes Research and Wellness Foundation; National Institute for Health and Care Research; Wellcome Trust","keywords":"Biology; Allele; Type 2 diabetes; Pancreatic islets; Locus (genetics); Insulin; Endocrinology; Diabetes mellitus; Internal medicine; Islet; Genetics; Gene; Medicine","score_opus":0.009097353582385954,"score_gpt":0.2770697199937989,"score_spread":0.267972366411413,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2883211905","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99622077,0.00025600303,0.0009295481,0.00027922064,0.00009461269,0.000013319434,0.00041079722,0.00007895513,0.0017167319],"genre_scores_gemma":[0.9969422,0.00014093448,0.00081094884,0.00021822719,0.000027502007,0.00001368625,0.00021350826,0.000082360864,0.0015506571],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9995876,0.00014719812,0.0000459518,0.00008293875,0.00006215464,0.000074050324],"domain_scores_gemma":[0.99957746,0.00015491768,0.000109716246,0.000045326673,0.000020061025,0.00009253187],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00025756744,0.0005595136,0.0002796073,0.0003549253,0.00022685707,0.0007172033,0.00028504655,0.0009234287,0.010693354],"category_scores_gemma":[0.00088899594,0.00027589686,0.00045567716,0.00032246232,0.0002639765,0.00025660024,0.00054632255,0.0009877472,0.00092128833],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0049096025,0.00038072024,0.015628463,0.000109226676,0.00014172331,0.0016177054,0.00011337973,0.00037109596,0.96492475,0.00093456736,0.0006898324,0.010178968],"study_design_scores_gemma":[0.001397605,0.0033411845,0.4146571,0.00024314637,0.0011298582,0.019392725,0.00067381875,0.007919732,0.5324892,0.0044461354,0.014160373,0.00014909719],"about_ca_topic_score_codex":0.00048438646,"about_ca_topic_score_gemma":0.0004607133,"teacher_disagreement_score":0.010693354,"about_ca_system_score_codex":0.00017237305,"about_ca_system_score_gemma":0.00018502575,"threshold_uncertainty_score":0.0357728},"labels":[],"label_agreement":null},{"id":"W2883415719","doi":"10.1038/s41588-018-0205-x","title":"Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits","year":2018,"lang":"en","type":"review","venue":"Nature Genetics","topic":"Genetic Associations and Epidemiology","field":"Biochemistry, Genetics and Molecular Biology","cited_by":1500,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Université Laval; Institut universitaire de cardiologie et de pneumologie de Québec; McMaster University","funders":"National Institute of Diabetes and Digestive and Kidney Diseases; National Cancer Institute; National Heart, Lung, and Blood Institute; NIHR Cambridge Biomedical Research Centre; NIHR Oxford Biomedical Research Centre; NIHR Imperial Biomedical Research Centre; Medical Research Council; Canadian Institutes of Health Research; Horizon 2020 Framework Programme; National Institutes of Health; National Human Genome Research Institute; UK Dementia Research Institute; Novo Nordisk Fonden; China Scholarship Council; Novo Nordisk; Public Health England; Li Ka Shing Foundation; European Commission; National Medical Research Council; King's College London; Biotechnology and Biological Sciences Research Council; Wellcome Trust; Cancer Research UK; Imperial College Healthcare NHS Trust; Netherlands Heart Institute; GlaxoSmithKline; Imperial College London; National Institute for Health and Care Research; National Center for Research Resources; Cisco Systems; Agence Nationale de la Recherche; Ministero della Salute; Alzheimer's Society; Université Laval; British Heart Foundation; Brigham and Women's Hospital; British Lung Foundation; National Institute for Health Research Health Protection Research Unit; EU Joint Programme – Neurodegenerative Disease Research; Eunice Kennedy Shriver National Institute of Child Health and Human Development; ZonMw; U.S. Department of Veterans Affairs; Economic and Social Research Council; U.S. Department of Health and Human Services","keywords":"Blood pressure; Biology; Genome-wide association study; Genetic architecture; Quantitative trait locus; Disease; Pulse pressure; Genetics; Risk factor; Internal medicine; Single-nucleotide polymorphism; Genotype; Gene; Medicine; Endocrinology","score_opus":0.012542302628954899,"score_gpt":0.29119540991894016,"score_spread":0.27865310728998527,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2883415719","genre_codex":"review","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":null,"domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.0004071545,0.9955183,0.0005281722,0.0019520188,0.00051683927,0.0000053763433,0.00013191291,0.000017336737,0.0009228267],"genre_scores_gemma":[0.0017563433,0.9952798,0.0005989547,0.0010734058,0.0007049299,0.000009915927,0.00013965367,0.000004001108,0.00043295627],"study_design_codex":"design_other","study_design_gemma":"observational","domain_scores_codex":[0.9995975,0.00008091481,0.00005989944,0.00009784084,0.00012988634,0.000033926848],"domain_scores_gemma":[0.99786586,0.001465043,0.00019050494,0.000050907358,0.00031379616,0.000113957656],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0016458891,0.0010012992,0.0012560406,0.0017961338,0.00021368616,0.000922098,0.0010639213,0.0013739374,0.002645261],"category_scores_gemma":[0.003251584,0.0002264441,0.0005885286,0.0019276482,0.00072754134,0.0008345005,0.00087601005,0.0017295181,0.00081301364],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00012796007,0.000040449664,0.0037351311,0.008237025,0.00034168176,0.00034754042,0.0000668774,0.00020629377,0.0008154099,0.003486946,0.039801784,0.9427928],"study_design_scores_gemma":[0.00007890602,0.000108580054,0.013271884,0.007932547,0.0010115372,0.0026568042,0.00016236497,0.00013755473,0.00055505394,0.0072849076,0.966743,0.00005680619],"about_ca_topic_score_codex":0.0020126768,"about_ca_topic_score_gemma":0.0031030935,"teacher_disagreement_score":0.002645261,"about_ca_system_score_codex":0.0005063373,"about_ca_system_score_gemma":0.0016536147,"threshold_uncertainty_score":0.008849263},"labels":[],"label_agreement":null},{"id":"W2883573930","doi":"10.1038/s41588-018-0147-3","title":"Gene discovery and polygenic prediction from a genome-wide association study of educational attainment in 1.1 million individuals","year":2018,"lang":"en","type":"review","venue":"Nature Genetics","topic":"Genetic Associations and Epidemiology","field":"Biochemistry, Genetics and Molecular Biology","cited_by":2846,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Queen's University; University of Toronto","funders":"National Institute on Aging; Eunice Kennedy Shriver National Institute of Child Health and Human Development; Economic and Social Research Council; Biotechnology and Biological Sciences Research Council; Medical Research Council; Lundbeckfonden; Karolinska Institutet; National Institute for Health and Care Research; Novo Nordisk Fonden; Open Philanthropy Project; National Institutes of Health; National Institute of Mental Health; Vetenskapsrådet; Wellcome Trust","keywords":"Genome-wide association study; Biology; Single-nucleotide polymorphism; Educational attainment; Multifactorial Inheritance; Heritability; Genetic association; Genetics; SNP; Gene; Genotype","score_opus":0.013191880786234641,"score_gpt":0.303236703263849,"score_spread":0.2900448224776144,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2883573930","genre_codex":"review","genre_gemma":"review","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"review","genre_consensus":"review","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.00021342024,0.99772936,0.0005108056,0.0008381191,0.00018826332,0.000004877538,0.000048212674,0.000009941601,0.0004570312],"genre_scores_gemma":[0.0018632145,0.99637115,0.0005678605,0.0004130591,0.00026454622,0.000010073868,0.00009997137,0.0000034025402,0.00040670118],"study_design_codex":"design_other","study_design_gemma":"observational","domain_scores_codex":[0.9995167,0.00013286537,0.00007129876,0.00012478227,0.00012876342,0.000025615074],"domain_scores_gemma":[0.99798477,0.001360502,0.00016478513,0.000055628585,0.00035678342,0.00007756806],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00215929,0.00081149157,0.0013030532,0.0027164654,0.00024606223,0.00092021626,0.0010556867,0.0013199395,0.0018289952],"category_scores_gemma":[0.0042171218,0.00031667924,0.0006951003,0.0017067712,0.00070840545,0.00082134205,0.00072335114,0.0017122674,0.0012233218],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0001267075,0.000029471574,0.0022746194,0.007968482,0.0005574221,0.0003031487,0.000059347996,0.00042842075,0.0005299703,0.0064886985,0.0198202,0.9614135],"study_design_scores_gemma":[0.000085840074,0.00016079274,0.012773758,0.008567553,0.0013756809,0.0034125748,0.00010408991,0.0005550723,0.000985268,0.01519363,0.95669806,0.00008765951],"about_ca_topic_score_codex":0.0022042864,"about_ca_topic_score_gemma":0.0028143188,"teacher_disagreement_score":0.0027164654,"about_ca_system_score_codex":0.00079896324,"about_ca_system_score_gemma":0.0015967664,"threshold_uncertainty_score":0.011419535},"labels":[],"label_agreement":null},{"id":"W2883945062","doi":"10.1038/s41588-018-0160-6","title":"Deep learning sequence-based ab initio prediction of variant effects on expression and disease risk","year":2018,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Genetic Associations and Epidemiology","field":"Biochemistry, Genetics and Molecular Biology","cited_by":605,"is_retracted":false,"has_abstract":false,"route_ca_aff":false,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"","funders":"National Institute of Allergy and Infectious Diseases; National Human Genome Research Institute; National Institute of General Medical Sciences; Canadian Institute for Advanced Research; National Heart, Lung, and Blood Institute; Princeton University","keywords":"Biology; In silico; Genetics; Computational biology; Human genome; Gene; Mutation; DNA microarray; Genome; Gene expression","score_opus":0.007847174803079521,"score_gpt":0.25591642277264465,"score_spread":0.24806924796956512,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2883945062","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.5955096,0.0024651918,0.39301848,0.0015267353,0.00018564655,0.000052801097,0.003021325,0.0019339153,0.0022862274],"genre_scores_gemma":[0.9688849,0.0004553411,0.026499307,0.00031955258,0.000097165226,0.0000466727,0.0020650055,0.0000612492,0.0015709283],"study_design_codex":"simulation_or_modeling","study_design_gemma":"simulation_or_modeling","domain_scores_codex":[0.9997514,0.00008467286,0.000014431393,0.00007487376,0.000030556883,0.000044107786],"domain_scores_gemma":[0.9986337,0.0010820637,0.00007209018,0.000072466886,0.00008415691,0.000055434946],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00091113884,0.0004996543,0.0009033078,0.00073944475,0.00025706404,0.00065496715,0.0007947629,0.0008560879,0.0022044794],"category_scores_gemma":[0.0026993093,0.00045553272,0.0010474025,0.00061823684,0.0003822684,0.00048431463,0.0005358068,0.0014934238,0.00053399993],"study_design_candidate":"simulation_or_modeling","study_design_consensus":"simulation_or_modeling","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0019556978,0.0006590957,0.07778153,0.00029924972,0.0009501325,0.00070747227,0.00014820152,0.66740644,0.020830339,0.013889425,0.0049084225,0.21046399],"study_design_scores_gemma":[0.000042880147,0.000041990665,0.0030391607,0.000013482548,0.00006518494,0.000054964556,0.000007645295,0.98336834,0.0012750226,0.011768737,0.0003142519,0.000008292307],"about_ca_topic_score_codex":0.006644382,"about_ca_topic_score_gemma":0.010593894,"teacher_disagreement_score":0.006644382,"about_ca_system_score_codex":0.00052077905,"about_ca_system_score_gemma":0.0008517088,"threshold_uncertainty_score":0.0132113695},"labels":[],"label_agreement":null},{"id":"W2890879010","doi":"10.1038/s41588-018-0211-z","title":"Promoter capture Hi-C-based identification of recurrent noncoding mutations in colorectal cancer","year":2018,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Cancer Genomics and Diagnostics","field":"Biochemistry, Genetics and Molecular Biology","cited_by":75,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"McGill University and Génome Québec Innovation Centre","funders":"","keywords":"Biology; Enhancer; Genetics; Genome; Gene; Chromosome conformation capture; Regulatory sequence; Computational biology; Cancer; Colorectal cancer; Promoter; Coding region; Regulation of gene expression; Cancer research; Gene expression","score_opus":0.00783735357466321,"score_gpt":0.28541348920980786,"score_spread":0.27757613563514466,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2890879010","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9834817,0.0014530944,0.010589569,0.00015511562,0.000029659184,0.000100407706,0.0012409522,0.00029295604,0.002656696],"genre_scores_gemma":[0.9866117,0.00042369074,0.0104429405,0.00017426614,0.000013144122,0.000044451917,0.0013000346,0.000041974035,0.00094776734],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9996216,0.000052701173,0.000019231848,0.000108132896,0.000115868126,0.00008247879],"domain_scores_gemma":[0.99946064,0.00020627913,0.00009216001,0.00006866892,0.00010178908,0.000070395436],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0003771952,0.00021755148,0.0002940561,0.0011379502,0.00019120144,0.00040035453,0.0003710443,0.00046418674,0.0012237371],"category_scores_gemma":[0.0010782172,0.00022940825,0.00024877622,0.00048309605,0.0002554666,0.00014231387,0.00030034964,0.00046044675,0.0005643032],"study_design_candidate":"bench_or_experimental","study_design_consensus":"bench_or_experimental","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00060017395,0.00007175621,0.03971428,0.0000916998,0.000069478425,0.0005090594,0.00007510754,0.00046435892,0.9399043,0.00014039954,0.0003922109,0.017967153],"study_design_scores_gemma":[0.00008531198,0.0006660837,0.22788836,0.000032149906,0.00027247058,0.0073546544,0.00015509175,0.016618254,0.741893,0.00027350438,0.0047275648,0.00003356632],"about_ca_topic_score_codex":0.0019634436,"about_ca_topic_score_gemma":0.0056502796,"teacher_disagreement_score":0.0019634436,"about_ca_system_score_codex":0.0003281917,"about_ca_system_score_gemma":0.00030820936,"threshold_uncertainty_score":0.004093826},"labels":[],"label_agreement":null},{"id":"W2891183151","doi":"10.1038/s41588-018-0233-6","title":"Reply to ‘Mutations in RECQL are not associated with breast cancer risk in an Australian population’","year":2018,"lang":"en","type":"letter","venue":"Nature Genetics","topic":"DNA Repair Mechanisms","field":"Biochemistry, Genetics and Molecular Biology","cited_by":2,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Mount Sinai Hospital; Ontario Tobacco Research Unit; Public Health Ontario; Women's College Hospital; University of Toronto","funders":"","keywords":"Biology; Breast cancer; Genetics; Population; Cancer; Environmental health; Medicine","score_opus":0.010484236426749935,"score_gpt":0.2771366342163746,"score_spread":0.26665239778962463,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2891183151","genre_codex":"commentary","genre_gemma":"commentary","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"commentary","genre_consensus":"commentary","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.0011253117,0.000598602,0.000055732395,0.98234093,0.014920525,0.0000055163864,0.00007529986,0.000011795752,0.0008662313],"genre_scores_gemma":[0.010096769,0.0006751002,0.00013826598,0.95693445,0.026485441,0.000030071613,0.000053121403,0.000021680187,0.0055650137],"study_design_codex":"not_applicable","study_design_gemma":"not_applicable","domain_scores_codex":[0.9977703,0.00059841346,0.00029237597,0.0003848902,0.0004490548,0.00050498336],"domain_scores_gemma":[0.99111617,0.0051247594,0.0009475545,0.00027607539,0.001307801,0.0012276792],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0028699026,0.00067019946,0.0012143973,0.0007201391,0.0031105797,0.0021112093,0.0015687422,0.032710515,0.00510658],"category_scores_gemma":[0.02888749,0.0008031727,0.00068140874,0.00075411884,0.00253944,0.002106125,0.0018116134,0.032631144,0.0030555571],"study_design_candidate":"not_applicable","study_design_consensus":"not_applicable","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00011416753,0.00003914581,0.004434423,0.000080091144,0.000036555895,0.0030176572,0.00056395243,0.000059773287,0.0002516756,0.0011513855,0.9835497,0.0067014163],"study_design_scores_gemma":[0.00035207535,0.00029377482,0.024948694,0.0007855676,0.00020290662,0.00936264,0.0037433866,0.00087843253,0.00077834894,0.011893496,0.9464968,0.00026390422],"about_ca_topic_score_codex":0.010983513,"about_ca_topic_score_gemma":0.014075698,"teacher_disagreement_score":0.032710515,"about_ca_system_score_codex":0.0028406412,"about_ca_system_score_gemma":0.0025412985,"threshold_uncertainty_score":0.021839201},"labels":[],"label_agreement":null},{"id":"W2893655504","doi":"10.1038/s41588-018-0238-1","title":"Integrative transcriptome analyses of the aging brain implicate altered splicing in Alzheimer’s disease susceptibility","year":2018,"lang":"en","type":"article","venue":"Nature Genetics","topic":"RNA Research and Splicing","field":"Biochemistry, Genetics and Molecular Biology","cited_by":456,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of British Columbia","funders":"National Institute on Aging; National Institutes of Health; National Institute of Mental Health; Nature","keywords":"RNA splicing; Biology; Alternative splicing; Transcriptome; Dorsolateral prefrontal cortex; Genetics; Prefrontal cortex; Aging brain; Alzheimer's disease; Genome-wide association study; Quantitative trait locus; Disease; Gene; Neuroscience; Gene expression; Single-nucleotide polymorphism; Messenger RNA; Medicine; Internal medicine; Genotype; RNA","score_opus":0.03091623631910586,"score_gpt":0.3700228972027143,"score_spread":0.33910666088360847,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2893655504","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.991891,0.0010076623,0.005076723,0.000105314604,0.000025286763,0.0000044599833,0.0010456756,0.000058808622,0.0007850686],"genre_scores_gemma":[0.9917277,0.00089363474,0.00512788,0.00010357673,0.000023229,0.0000099198805,0.0012738127,0.00006192758,0.0007784118],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9998541,0.000020019288,0.0000108316435,0.00005803976,0.000036349877,0.000020578324],"domain_scores_gemma":[0.9997991,0.000050286322,0.000061745915,0.000029564993,0.000033778968,0.0000256644],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0004079358,0.0003244801,0.0003521016,0.0005006994,0.00021993325,0.0003872363,0.0001592368,0.0002188211,0.0009643188],"category_scores_gemma":[0.00024713224,0.00017084264,0.0003970246,0.00038117016,0.0002512117,0.00024602422,0.00025923213,0.00034840323,0.00016050281],"study_design_candidate":"bench_or_experimental","study_design_consensus":"bench_or_experimental","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00027666127,0.000028224402,0.010490904,0.000051579762,0.00012321048,0.00016503916,0.00011723092,0.00035978903,0.98022825,0.0007010076,0.00020092037,0.007257221],"study_design_scores_gemma":[0.000048078855,0.00038241144,0.70944506,0.000031964624,0.0006331861,0.0014162079,0.00036557755,0.006748048,0.26850724,0.0063897227,0.0059907194,0.000041832427],"about_ca_topic_score_codex":0.00067038496,"about_ca_topic_score_gemma":0.001630686,"teacher_disagreement_score":0.0009643188,"about_ca_system_score_codex":0.00022369987,"about_ca_system_score_gemma":0.00016684915,"threshold_uncertainty_score":0.0032259226},"labels":[],"label_agreement":null},{"id":"W2895074862","doi":"10.1038/s41588-018-0237-2","title":"Allele-defined genome of the autopolyploid sugarcane Saccharum spontaneum L.","year":2018,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Sugarcane Cultivation and Processing","field":"Agricultural and Biological Sciences","cited_by":795,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Ottawa","funders":"National High-tech Research and Development Program; Biological and Environmental Research; Program for New Century Excellent Talents in University; Office of Science; Fujian Agriculture and Forestry University; National Natural Science Foundation of China; European Bioinformatics Institute; Fundação de Amparo à Pesquisa do Estado de São Paulo; U.S. Department of Energy; National Science Foundation","keywords":"Biology; Polyploid; Genome; Genetics; Chromosome; Ploidy; Homologous chromosome; Saccharum; Gene; Saccharum officinarum; Botany","score_opus":0.013625378950974286,"score_gpt":0.23050701610671756,"score_spread":0.21688163715574327,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2895074862","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9754404,0.0006490701,0.008250706,0.000074451425,0.000024821507,0.000064655535,0.012720556,0.00028065644,0.0024947023],"genre_scores_gemma":[0.9338901,0.00050325535,0.0102490345,0.0000729156,0.000010050014,0.00008310103,0.049863998,0.00012489881,0.005202741],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9999484,0.0000036568595,0.0000029767962,0.000019713822,0.000017650975,0.000007580911],"domain_scores_gemma":[0.99995327,0.0000085414895,0.000011639956,0.000009570777,0.000006969632,0.000009972669],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.000051777228,0.00028592517,0.00015799857,0.00031546096,0.00023337116,0.00019337794,0.00018662626,0.00016176068,0.0013477857],"category_scores_gemma":[0.000100481,0.0001023829,0.00018052703,0.0005295416,0.00010612464,0.00010222769,0.00019814887,0.0002859549,0.000341337],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00007649669,0.0000107736205,0.00057312835,0.00004506548,0.000009161923,0.00006986731,0.000036959682,0.00011040302,0.9947419,0.00017684414,0.00006612224,0.0040833754],"study_design_scores_gemma":[0.00007949279,0.00036863392,0.20851381,0.000034371686,0.0002395174,0.0020026278,0.00028577505,0.004233652,0.72025377,0.0009719966,0.062966496,0.00004980741],"about_ca_topic_score_codex":0.0025262896,"about_ca_topic_score_gemma":0.0048516975,"teacher_disagreement_score":0.0025262896,"about_ca_system_score_codex":0.0002422393,"about_ca_system_score_gemma":0.00035312603,"threshold_uncertainty_score":0.0050231814},"labels":[],"label_agreement":null},{"id":"W2896958236","doi":"10.1038/s41588-019-0403-1","title":"Maternal and fetal genetic effects on birth weight and their relevance to cardio-metabolic risk factors","year":2019,"lang":"en","type":"review","venue":"Nature Genetics","topic":"Birth, Development, and Health","field":"Medicine","cited_by":649,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Cégep de Chicoutimi; Université de Sherbrooke; Centre Hospitalier Universitaire de Sherbrooke","funders":"National Institute of Diabetes and Digestive and Kidney Diseases; Medical Research Council; National Institute of Environmental Health Sciences; Servier; Lundbeckfonden; Universitat Pompeu Fabra; National Institute for Health and Care Research; University of Southampton; Novo Nordisk Fonden; Sidra Medicine; Diabetes UK; Eli Lilly and Company; University Hospital Southampton NHS Foundation Trust; Wellcome Trust; Steno Diabetes Center Copenhagen; National Institute for Health Research Southampton Biomedical Research Centre; Sanofi; Pfizer","keywords":"Offspring; Mendelian randomization; Biology; Birth weight; Fetus; Blood pressure; Allele; Maternal effect; Low birth weight; Physiology; Genetics; Pregnancy; Genotype; Obstetrics; Endocrinology; Medicine; Gene; Genetic variants","score_opus":0.014517255451610733,"score_gpt":0.29683526783504444,"score_spread":0.2823180123834337,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2896958236","genre_codex":"review","genre_gemma":"review","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"review","genre_consensus":"review","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.000069981026,0.99905545,0.00008034405,0.00032599972,0.00014623167,0.0000011446939,0.000018249599,0.0000031422026,0.0002993305],"genre_scores_gemma":[0.0004180613,0.9989359,0.00008986705,0.00014834909,0.00021008647,0.0000024682454,0.000020065709,7.583306e-7,0.0001744727],"study_design_codex":"design_other","study_design_gemma":"systematic_review","domain_scores_codex":[0.99978966,0.000051878287,0.000031046024,0.000047664613,0.000060434188,0.00001945651],"domain_scores_gemma":[0.99912375,0.00062770804,0.00008568414,0.000019693865,0.0001009425,0.000042223324],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0009653571,0.0010188862,0.0017963671,0.001440246,0.00016973996,0.0007761876,0.0009208223,0.0011515219,0.0026749338],"category_scores_gemma":[0.0015153519,0.00026636483,0.00044862082,0.0019950487,0.0006400778,0.00063340156,0.000759113,0.0017591035,0.000918523],"study_design_candidate":"systematic_review","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00016211753,0.0000542727,0.0008882821,0.011889152,0.0003006162,0.00027160638,0.000057196703,0.0005252438,0.00082579977,0.0054888395,0.027651308,0.9518855],"study_design_scores_gemma":[0.00006376717,0.00010542052,0.006320209,0.010461122,0.00079044135,0.0016874219,0.0001268268,0.00020276124,0.00038297754,0.009406757,0.9703945,0.00005782835],"about_ca_topic_score_codex":0.0020795332,"about_ca_topic_score_gemma":0.0030533327,"teacher_disagreement_score":0.0026749338,"about_ca_system_score_codex":0.00062299304,"about_ca_system_score_gemma":0.00096106593,"threshold_uncertainty_score":0.0089485645},"labels":[],"label_agreement":null},{"id":"W2897450736","doi":"10.1038/s41588-018-0251-4","title":"Germline HAVCR2 mutations altering TIM-3 characterize subcutaneous panniculitis-like T cell lymphomas with hemophagocytic lymphohistiocytic syndrome","year":2018,"lang":"en","type":"letter","venue":"Nature Genetics","topic":"Galectins and Cancer Biology","field":"Immunology and Microbiology","cited_by":218,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"McGill Genome Centre; Montreal Children's Hospital; McGill University and Génome Québec Innovation Centre; Ontario Genomics; Sinai Health System; McGill University Health Centre; Lunenfeld-Tanenbaum Research Institute; University of Toronto; McGill University","funders":"Nature; Agence Nationale de la Recherche; Fonds de Recherche du Québec - Santé; European Bioinformatics Institute","keywords":"Biology; Germline; Germline mutation; Cancer research; Mutation; Genetics; Gene","score_opus":0.0065472470830986946,"score_gpt":0.21280377520074734,"score_spread":0.20625652811764864,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2897450736","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.5899231,0.005902061,0.007277452,0.28482115,0.013847391,0.0002811725,0.0006623302,0.00078700663,0.09649841],"genre_scores_gemma":[0.96641904,0.0010795596,0.0015476871,0.01918408,0.006098421,0.000024044415,0.00008440493,0.00006784921,0.0054949163],"study_design_codex":"case_report","study_design_gemma":"observational","domain_scores_codex":[0.9996964,0.00005736689,0.00002433101,0.00005265939,0.000058175006,0.00011112763],"domain_scores_gemma":[0.999199,0.00039225712,0.000099080855,0.00007802739,0.00009825844,0.0001333683],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00039796112,0.00064003846,0.0004195553,0.00040755115,0.0006239676,0.0008248935,0.000518554,0.004709557,0.002394685],"category_scores_gemma":[0.0027134612,0.00027454837,0.00033750886,0.0003117518,0.000992676,0.0007093452,0.00041961507,0.0025286938,0.0009742995],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00041175878,0.00009020193,0.022696508,0.00008436,0.00004278787,0.90021485,0.00026176125,0.00034613055,0.00954997,0.0040647956,0.047409784,0.014827077],"study_design_scores_gemma":[0.00026467998,0.00016817267,0.017386818,0.000087365064,0.000076569406,0.92246884,0.0003443329,0.003973941,0.004617625,0.006696992,0.04387504,0.000039717776],"about_ca_topic_score_codex":0.00091896154,"about_ca_topic_score_gemma":0.0010441352,"teacher_disagreement_score":0.004709557,"about_ca_system_score_codex":0.0007829884,"about_ca_system_score_gemma":0.00027246046,"threshold_uncertainty_score":0.0080109835},"labels":[],"label_agreement":null},{"id":"W2897548162","doi":"10.1038/s41588-018-0124-x","title":"Publisher Correction: Ancient hybridization and strong adaptation to viruses across African vervet monkey populations","year":2018,"lang":"en","type":"erratum","venue":"Nature Genetics","topic":"Virology and Viral Diseases","field":"Medicine","cited_by":0,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"McGill University","funders":"","keywords":"Biology; Adaptation (eye); Vervet monkey; Evolutionary biology; Zoology; Virology; Genetics; Neuroscience","score_opus":0.0408986090228675,"score_gpt":0.3423044337733148,"score_spread":0.3014058247504473,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2897548162","genre_codex":"editorial","genre_gemma":"other","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"other","genre_consensus":null,"domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.00030406553,0.000681088,0.00097406335,0.02208067,0.9712043,0.0000149275975,0.0009494533,0.00036062798,0.0034308748],"genre_scores_gemma":[0.033469934,0.011527905,0.014590688,0.058003653,0.38157195,0.0002009883,0.006546137,0.004328724,0.48975992],"study_design_codex":"not_applicable","study_design_gemma":"not_applicable","domain_scores_codex":[0.99775547,0.0002938963,0.0003950642,0.00043418992,0.0009258638,0.00019557877],"domain_scores_gemma":[0.98529124,0.0042442847,0.000743128,0.0012138181,0.007881329,0.0006262359],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.002054546,0.0017096202,0.0012667418,0.0024579815,0.0029415928,0.002960973,0.002567078,0.0039308006,0.07193206],"category_scores_gemma":[0.034221232,0.0008428085,0.001065895,0.0018586604,0.0014293649,0.0020970332,0.0016609171,0.007713481,0.030995712],"study_design_candidate":"not_applicable","study_design_consensus":"not_applicable","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00003519962,0.0000062360755,0.00009844638,0.00012174418,0.000011858575,0.0003992131,0.000045624776,0.000049490995,0.0001345818,0.0009442604,0.9875464,0.010606916],"study_design_scores_gemma":[0.000021899226,0.00001576109,0.00070362503,0.0002860866,0.000034019322,0.001009084,0.00008280887,0.00019168078,0.00064876914,0.001461545,0.9955107,0.00003404821],"about_ca_topic_score_codex":0.008948195,"about_ca_topic_score_gemma":0.014143654,"teacher_disagreement_score":0.07193206,"about_ca_system_score_codex":0.0020479378,"about_ca_system_score_gemma":0.0027884583,"threshold_uncertainty_score":0.2406367},"labels":[],"label_agreement":null},{"id":"W2897661414","doi":"10.1038/s41588-018-0246-1","title":"Investigation of inter- and intraspecies variation through genome sequencing of Aspergillus section Nigri","year":2018,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Microbial Natural Products and Biosynthesis","field":"Medicine","cited_by":235,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Concordia University","funders":"Biological and Environmental Research; Novo Nordisk Fonden; Lawrence Berkeley National Laboratory; Novo Nordisk; National Research Foundation; Joint Genome Institute; Office of Science; Danmarks Grundforskningsfond; Villum Fonden; U.S. Department of Energy","keywords":"Biology; Aspergillus; Genome; Compendium; Metabolomics; Aspergillus nidulans; Genetics; Secondary metabolite; Secondary metabolism; Genomics; Computational biology; Gene; Bioinformatics","score_opus":0.018914669200933425,"score_gpt":0.24364949712503953,"score_spread":0.2247348279241061,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2897661414","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99188656,0.00014406806,0.0048755053,0.000028941533,0.0000034720053,0.0000130792905,0.00258263,0.000060594295,0.00040526758],"genre_scores_gemma":[0.9608879,0.0002058376,0.023408188,0.000042766518,0.0000049237274,0.000034330584,0.015100251,0.000056626184,0.0002592208],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9996393,0.00007833054,0.00002732822,0.00015190637,0.00006932041,0.000033781394],"domain_scores_gemma":[0.9993574,0.00030029548,0.00011426511,0.000096197386,0.000084486346,0.00004742451],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.000607642,0.00025777062,0.00038490145,0.00070671167,0.00024367782,0.00039489567,0.00032003943,0.0002338313,0.00024313245],"category_scores_gemma":[0.0012397469,0.0001714149,0.0005599646,0.00092479034,0.0001646357,0.00016983257,0.00030751433,0.00036768682,0.00013033161],"study_design_candidate":"bench_or_experimental","study_design_consensus":"bench_or_experimental","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0005553904,0.0001602503,0.11952227,0.00022722878,0.00056593795,0.00063520944,0.0005848465,0.023069523,0.81256783,0.0012745358,0.0005056207,0.04033127],"study_design_scores_gemma":[0.000056462864,0.0002684908,0.85253954,0.000047668444,0.00041737358,0.001120823,0.0003857664,0.079499215,0.05349226,0.0014012613,0.010712715,0.00005846451],"about_ca_topic_score_codex":0.0029396622,"about_ca_topic_score_gemma":0.005950985,"teacher_disagreement_score":0.0029396622,"about_ca_system_score_codex":0.00034463627,"about_ca_system_score_gemma":0.0003397653,"threshold_uncertainty_score":0.0058451295},"labels":[],"label_agreement":null},{"id":"W2898477312","doi":"10.1038/s41588-018-0276-8","title":"Author Correction: Discovery and refinement of genetic loci associated with cardiometabolic risk using dense imputation maps","year":2018,"lang":"en","type":"erratum","venue":"Nature Genetics","topic":"Nutrition, Genetics, and Disease","field":"Biochemistry, Genetics and Molecular Biology","cited_by":2,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"McGill University; Jewish General Hospital","funders":"Medical Research Council","keywords":"Imputation (statistics); Biology; Computational biology; Genetics; Genome-wide association study; Evolutionary biology; Computer science; Single-nucleotide polymorphism; Machine learning; Missing data; Gene; Genotype","score_opus":0.0068647326846815885,"score_gpt":0.25354930211362103,"score_spread":0.24668456942893943,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2898477312","genre_codex":"editorial","genre_gemma":"other","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"other","genre_consensus":null,"domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.00090163114,0.0009711968,0.010603219,0.04598426,0.9207881,0.000088379034,0.01372534,0.0022598323,0.0046779737],"genre_scores_gemma":[0.0721851,0.0060063777,0.08269452,0.074646704,0.18990162,0.0011696575,0.045395695,0.020174583,0.50782573],"study_design_codex":"not_applicable","study_design_gemma":"not_applicable","domain_scores_codex":[0.99324256,0.0015359004,0.0012952068,0.0011108172,0.0022156043,0.0005998576],"domain_scores_gemma":[0.94790417,0.01872715,0.0020303682,0.006571565,0.023134196,0.0016326079],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.008704111,0.002381187,0.0023389803,0.003704119,0.0032114782,0.0040883143,0.0052298214,0.0049672085,0.201267],"category_scores_gemma":[0.14561716,0.0017757482,0.0024592762,0.0034645542,0.0017458934,0.0024605514,0.0031952187,0.008589748,0.05599086],"study_design_candidate":"not_applicable","study_design_consensus":"not_applicable","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00010442287,0.000009212127,0.00044008726,0.0002127648,0.000076158445,0.00041765446,0.00006389917,0.00015572694,0.00009964442,0.0013493454,0.98832524,0.008745977],"study_design_scores_gemma":[0.00045398917,0.000043025015,0.0031939922,0.0009768733,0.00035734652,0.002711731,0.00021564722,0.0017552982,0.0013375349,0.011880477,0.9769349,0.00013900013],"about_ca_topic_score_codex":0.01163005,"about_ca_topic_score_gemma":0.020450473,"teacher_disagreement_score":0.201267,"about_ca_system_score_codex":0.0022502344,"about_ca_system_score_gemma":0.0054668193,"threshold_uncertainty_score":0.6733052},"labels":[],"label_agreement":null},{"id":"W2898969969","doi":"10.1038/s41588-018-0258-x","title":"Neutral tumor evolution?","year":2018,"lang":"en","type":"letter","venue":"Nature Genetics","topic":"Cancer Genomics and Diagnostics","field":"Biochemistry, Genetics and Molecular Biology","cited_by":77,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Vector Institute; University of Toronto","funders":"Medical Research Council; Hutchison Whampoa Limited; Wellcome Trust; Francis Crick Institute; National Cancer Institute; Cancer Research UK; European Commission; Li Ka Shing Foundation","keywords":"Biology; Neutral theory of molecular evolution; Positive selection; Neutral mutation; Genetics; Selection (genetic algorithm); Cancer; Genome; Evolutionary biology; Computational biology; Gene","score_opus":0.004684326807179373,"score_gpt":0.23668729593053134,"score_spread":0.23200296912335197,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2898969969","genre_codex":"commentary","genre_gemma":"commentary","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"commentary","genre_consensus":"commentary","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.0064254617,0.0070080934,0.002721023,0.95278955,0.012586599,0.000012488524,0.00008685155,0.000111194946,0.01825868],"genre_scores_gemma":[0.18650877,0.0050389753,0.0016865194,0.74712026,0.036184896,0.000054487264,0.000120477394,0.0001126807,0.023172978],"study_design_codex":"not_applicable","study_design_gemma":"not_applicable","domain_scores_codex":[0.99909735,0.00021311916,0.000051182607,0.00020398168,0.00024460323,0.00018970203],"domain_scores_gemma":[0.9963552,0.0018760293,0.00023109568,0.00036968326,0.00038356296,0.0007844873],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0032047674,0.00026179664,0.00043131318,0.00025446335,0.0010315016,0.0016662643,0.0007811889,0.009430145,0.00567877],"category_scores_gemma":[0.01257041,0.00014240769,0.00029848644,0.00015497972,0.0034342667,0.002392886,0.0015931868,0.010935048,0.0016839467],"study_design_candidate":"not_applicable","study_design_consensus":"not_applicable","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00035277332,0.00006083382,0.0048698997,0.00011698693,0.000110319284,0.0049366504,0.00042744848,0.0005071792,0.00259895,0.2741433,0.59601355,0.115862094],"study_design_scores_gemma":[0.00016431206,0.00006629425,0.0018469073,0.00012521559,0.000040829964,0.0052926033,0.00030265682,0.0013415468,0.0013848864,0.34196225,0.64743674,0.000035796264],"about_ca_topic_score_codex":0.0008178876,"about_ca_topic_score_gemma":0.0011429399,"teacher_disagreement_score":0.009430145,"about_ca_system_score_codex":0.0017089661,"about_ca_system_score_gemma":0.0009878079,"threshold_uncertainty_score":0.018997371},"labels":[],"label_agreement":null},{"id":"W2898972432","doi":"10.1038/s41588-018-0254-1","title":"Identification of phagocytosis regulators using magnetic genome-wide CRISPR screens","year":2018,"lang":"en","type":"article","venue":"Nature Genetics","topic":"CRISPR and Genetic Engineering","field":"Biochemistry, Genetics and Molecular Biology","cited_by":204,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Toronto","funders":"Eunice Kennedy Shriver National Institute of Child Health and Human Development; National Institute of General Medical Sciences; National Institute on Drug Abuse; National Institutes of Health","keywords":"Phagocytosis; Biology; Filopodia; RAC1; Phagosome; Cell biology; Gene; Actin; Genetics; Signal transduction","score_opus":0.006954892547312249,"score_gpt":0.29358703752723875,"score_spread":0.2866321449799265,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2898972432","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.8818665,0.0024769176,0.09242269,0.0013327041,0.00033257648,0.00047089488,0.0022487068,0.0025368796,0.016312083],"genre_scores_gemma":[0.96801794,0.00079209456,0.022051165,0.00046289217,0.000030611518,0.00017594523,0.0010063502,0.0001986035,0.007264459],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99905187,0.000093442824,0.00007550031,0.00020036475,0.00041989225,0.0001588343],"domain_scores_gemma":[0.99943215,0.00014678416,0.0001624455,0.00008121296,0.00008568837,0.00009177427],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00071404845,0.00076197286,0.0007474291,0.00086330425,0.00072867447,0.001293957,0.00085356727,0.0008581223,0.002198285],"category_scores_gemma":[0.0006397354,0.00040617332,0.00066439575,0.00037948205,0.0007951073,0.00034863583,0.000995865,0.0015324171,0.0009043222],"study_design_candidate":"bench_or_experimental","study_design_consensus":"bench_or_experimental","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00009557035,0.00006234665,0.00038398846,0.00004365859,0.0000157248,0.00008725537,0.000016849071,0.00019611519,0.9953548,0.0004539448,0.00020782751,0.003081936],"study_design_scores_gemma":[0.00003049717,0.00016576797,0.0029202679,0.000011256408,0.000043659817,0.00040359155,0.000045360335,0.0023107347,0.988103,0.00023995985,0.0057052234,0.000020683652],"about_ca_topic_score_codex":0.00097546756,"about_ca_topic_score_gemma":0.0033104694,"teacher_disagreement_score":0.002198285,"about_ca_system_score_codex":0.0010512087,"about_ca_system_score_gemma":0.0006843357,"threshold_uncertainty_score":0.00762707},"labels":[],"label_agreement":null},{"id":"W2900795735","doi":"10.1038/s41588-018-0265-y","title":"ROBO4 variants predispose individuals to bicuspid aortic valve and thoracic aortic aneurysm","year":2018,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Connective tissue disorders research","field":"Biochemistry, Genetics and Molecular Biology","cited_by":153,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Toronto; Hospital for Sick Children; Université de Montréal; SickKids Foundation; Centre Hospitalier Universitaire Sainte-Justine","funders":"National Institute of General Medical Sciences; National Heart, Lung, and Blood Institute; National Institutes of Health; Lundbeckfonden; National Human Genome Research Institute; Eunice Kennedy Shriver National Institute of Child Health and Human Development; Howard Hughes Medical Institute","keywords":"Bicuspid aortic valve; Thoracic aortic aneurysm; Biology; Internal medicine; Aortic aneurysm; Cardiology; Aortic valve; Aneurysm; Aorta; Radiology; Medicine","score_opus":0.012116627451902616,"score_gpt":0.33462664495324257,"score_spread":0.32251001750133995,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2900795735","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9933583,0.0011848566,0.001510775,0.00018250034,0.000051895262,0.000033468572,0.0005865484,0.00009842122,0.002993222],"genre_scores_gemma":[0.99661165,0.00049354084,0.0016056707,0.00010125511,0.00006248888,0.000021273992,0.0003029025,0.000023324881,0.00077777007],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99957687,0.00007661666,0.000037710444,0.00011906683,0.00011858341,0.00007122292],"domain_scores_gemma":[0.99951935,0.00017112555,0.00016223318,0.000024788202,0.000032960328,0.00008947209],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00020928998,0.0014259985,0.0005690275,0.0015707526,0.00082366506,0.00040277847,0.00042194096,0.0010357779,0.00564961],"category_scores_gemma":[0.0013009148,0.00033390147,0.0004287319,0.00073048734,0.0004855979,0.0002113277,0.000619435,0.00042904893,0.00040526653],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.002061813,0.00033586076,0.67960984,0.00037473405,0.00056088663,0.12865038,0.0016987957,0.0010741499,0.14652343,0.0020933764,0.0028534592,0.034163255],"study_design_scores_gemma":[0.00006316609,0.0002994963,0.7840978,0.00016859832,0.00037006073,0.20004696,0.0006170538,0.0010700366,0.008356704,0.0013306976,0.0035195102,0.000060011957],"about_ca_topic_score_codex":0.0023948937,"about_ca_topic_score_gemma":0.0020986232,"teacher_disagreement_score":0.00564961,"about_ca_system_score_codex":0.00014179117,"about_ca_system_score_gemma":0.00018675762,"threshold_uncertainty_score":0.018899798},"labels":[],"label_agreement":null},{"id":"W2901255973","doi":"10.1038/s41588-018-0304-8","title":"Author Correction: Germline HAVCR2 mutations altering TIM-3 characterize subcutaneous panniculitis-like T cell lymphomas with hemophagocytic lymphohistiocytic syndrome","year":2018,"lang":"en","type":"erratum","venue":"Nature Genetics","topic":"Galectins and Cancer Biology","field":"Immunology and Microbiology","cited_by":2,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"McGill Genome Centre; Montreal Children's Hospital; McGill University and Génome Québec Innovation Centre; Ontario Genomics; Sinai Health System; McGill University Health Centre; Lunenfeld-Tanenbaum Research Institute; University of Toronto; McGill University","funders":"","keywords":"Germline; Biology; Genetics; Germline mutation; Cancer research; Mutation; Gene","score_opus":0.007213591314757164,"score_gpt":0.23092073076451544,"score_spread":0.22370713944975829,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2901255973","genre_codex":"editorial","genre_gemma":"other","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"other","genre_consensus":null,"domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.00080348644,0.0011490263,0.0009226239,0.068114564,0.92584914,0.000020764195,0.0006072998,0.00028933346,0.0022437277],"genre_scores_gemma":[0.082765274,0.011210148,0.010399737,0.122091055,0.529693,0.00018702571,0.0025853568,0.0020188955,0.23904952],"study_design_codex":"not_applicable","study_design_gemma":"not_applicable","domain_scores_codex":[0.9982476,0.00022663125,0.00029402,0.00032008503,0.00068494456,0.00022665372],"domain_scores_gemma":[0.99168867,0.0025641753,0.00076112774,0.0004825751,0.0039428063,0.0005607218],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0018501196,0.001548315,0.0012461358,0.002038074,0.0018416581,0.0020974951,0.0026621823,0.007711591,0.022511765],"category_scores_gemma":[0.027244637,0.00084152375,0.0011131066,0.0008462765,0.0015635921,0.0015345766,0.0013069548,0.00835794,0.009751448],"study_design_candidate":"not_applicable","study_design_consensus":"not_applicable","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00006853473,0.000013751869,0.000314662,0.00017137238,0.000032932312,0.008734217,0.000061071085,0.00010128728,0.00022420575,0.0011934559,0.98029375,0.008790703],"study_design_scores_gemma":[0.00010993252,0.000039031464,0.0016892666,0.00047036173,0.00011937296,0.021972667,0.00016932376,0.00067593734,0.0013747538,0.002330031,0.9709779,0.00007142805],"about_ca_topic_score_codex":0.0052110166,"about_ca_topic_score_gemma":0.007263637,"teacher_disagreement_score":0.022511765,"about_ca_system_score_codex":0.0022060857,"about_ca_system_score_gemma":0.0019056313,"threshold_uncertainty_score":0.075309336},"labels":[],"label_agreement":null},{"id":"W2901302224","doi":"10.1038/s41588-018-0293-7","title":"Publisher Correction: Allele-defined genome of the autopolyploid sugarcane Saccharum spontaneum L","year":2018,"lang":"en","type":"erratum","venue":"Nature Genetics","topic":"Sugarcane Cultivation and Processing","field":"Agricultural and Biological Sciences","cited_by":18,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Ottawa","funders":"","keywords":"Biology; Genome; Accession number (library science); Accession; Section (typography); Annotation; Gene; Saccharum; Allele; Genetics; Computational biology; Botany; Computer science","score_opus":0.013325829304648228,"score_gpt":0.2247058631708381,"score_spread":0.21138003386618986,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2901302224","genre_codex":"editorial","genre_gemma":"other","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"other","genre_consensus":null,"domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.00049687934,0.00079969264,0.0014588262,0.013995546,0.9764068,0.000016259977,0.0015033375,0.0006429036,0.0046797576],"genre_scores_gemma":[0.03500035,0.008301923,0.016158532,0.029236484,0.22017615,0.00019149175,0.0123086795,0.0051545654,0.67347187],"study_design_codex":"not_applicable","study_design_gemma":"not_applicable","domain_scores_codex":[0.99880147,0.000115156305,0.0001872531,0.0002160901,0.0005767424,0.00010318441],"domain_scores_gemma":[0.9912211,0.001611885,0.00040699646,0.00082915113,0.0054294383,0.0005014466],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0011376614,0.0015013303,0.0012644768,0.0027481944,0.0023793695,0.0025314617,0.002839072,0.0030822998,0.0531471],"category_scores_gemma":[0.014256608,0.0008410528,0.0011648557,0.0016997593,0.0011096584,0.0015911569,0.0014333992,0.0059900205,0.021759668],"study_design_candidate":"not_applicable","study_design_consensus":"not_applicable","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.000063667016,0.00001058159,0.000110118,0.0001739694,0.000017346947,0.0005850836,0.000030277366,0.000113266135,0.0004238297,0.0011426162,0.9851693,0.012159891],"study_design_scores_gemma":[0.000027736587,0.000016487951,0.0008911054,0.000111177986,0.00003650025,0.0006288266,0.000041218755,0.00025176094,0.0011996807,0.00090948236,0.99585885,0.00002723414],"about_ca_topic_score_codex":0.0129708275,"about_ca_topic_score_gemma":0.016886542,"teacher_disagreement_score":0.0531471,"about_ca_system_score_codex":0.002359647,"about_ca_system_score_gemma":0.0024906488,"threshold_uncertainty_score":0.17779481},"labels":[],"label_agreement":null},{"id":"W2901715532","doi":"10.1038/s41588-018-0297-3","title":"Publisher Correction: Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits","year":2018,"lang":"en","type":"erratum","venue":"Nature Genetics","topic":"Nutrition, Genetics, and Disease","field":"Biochemistry, Genetics and Molecular Biology","cited_by":38,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Université Laval; Institut universitaire de cardiologie et de pneumologie de Québec; McMaster University","funders":"Medical Research Council; Novo Nordisk Fonden; U.S. Department of Veterans Affairs; National Institute for Health and Care Research; British Heart Foundation; Cancer Research UK","keywords":"Biology; XML; Genetics; Computational biology; Genealogy; Computer science; World Wide Web; History","score_opus":0.004340808723581547,"score_gpt":0.22633554338354422,"score_spread":0.22199473465996267,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2901715532","genre_codex":"editorial","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":null,"domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.0001050591,0.00045406923,0.00048215897,0.025263278,0.9698014,0.00001593293,0.001096305,0.00031161815,0.002470126],"genre_scores_gemma":[0.013840697,0.0055452827,0.00790283,0.085133255,0.4079156,0.00031086805,0.006159022,0.0034276543,0.46976474],"study_design_codex":"not_applicable","study_design_gemma":"observational","domain_scores_codex":[0.9955391,0.0006755341,0.0007751982,0.00057527574,0.0020346595,0.00040017447],"domain_scores_gemma":[0.9647745,0.007018652,0.0015841487,0.0025241268,0.022694826,0.0014037082],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.004343203,0.002422597,0.0022061737,0.004733113,0.0035683094,0.0047834893,0.0047788173,0.006310766,0.10134628],"category_scores_gemma":[0.06256697,0.0014585075,0.0018778731,0.0028083138,0.0020249372,0.0025361124,0.0021254283,0.01226463,0.049127735],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00002057461,0.0000046223236,0.0000669561,0.00006578358,0.00000985104,0.00020221552,0.0000156326,0.000029470812,0.00002050464,0.0003863555,0.9958864,0.0032916379],"study_design_scores_gemma":[0.000071579685,0.000018791741,0.0009958813,0.00038417865,0.000055623106,0.00077670865,0.00007771406,0.00027515105,0.00030004172,0.001588248,0.99541336,0.00004256572],"about_ca_topic_score_codex":0.019333081,"about_ca_topic_score_gemma":0.026367096,"teacher_disagreement_score":0.10134628,"about_ca_system_score_codex":0.0038107235,"about_ca_system_score_gemma":0.004956682,"threshold_uncertainty_score":0.33903712},"labels":[],"label_agreement":null},{"id":"W2903533144","doi":"10.1038/s41588-018-0286-6","title":"Discovery of common and rare genetic risk variants for colorectal cancer","year":2018,"lang":"en","type":"review","venue":"Nature Genetics","topic":"Genetic factors in colorectal cancer","field":"Medicine","cited_by":605,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Memorial University of Newfoundland; Lunenfeld-Tanenbaum Research Institute; Ontario Institute for Cancer Research; University of Toronto; Mount Sinai Hospital","funders":"National Institute of Environmental Health Sciences; Center for Gastrointestinal Biology and Disease, School of Medicine, University of North Carolina at Chapel Hill; National Cancer Institute; National Heart, Lung, and Blood Institute; Medical Research Council; Johns Hopkins Bloomberg School of Public Health; University of Oxford; World Health Organization; University of North Carolina at Chapel Hill; Ohio State University; National Institutes of Health; Chonnam National University; Cancer Research UK; Invitae; Myriad Genetics; National Institute of Diabetes and Digestive and Kidney Diseases; Chonnam National University Hwasun Hospital; Johns Hopkins University","keywords":"Biology; Colorectal cancer; Genetics; Computational biology; Cancer; Bioinformatics","score_opus":0.02496198594517528,"score_gpt":0.35136572821633094,"score_spread":0.32640374227115565,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2903533144","genre_codex":"review","genre_gemma":"review","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"review","genre_consensus":"review","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.00016049235,0.998252,0.00017184981,0.0006537807,0.00027586467,0.0000023159569,0.000035616446,0.000007708491,0.00044035882],"genre_scores_gemma":[0.0013871067,0.99674404,0.00031300125,0.0006351271,0.0005802747,0.0000036063793,0.00006705544,0.000002512612,0.00026732794],"study_design_codex":"design_other","study_design_gemma":"meta_analysis","domain_scores_codex":[0.9995716,0.00006911783,0.00009076654,0.00009327485,0.00013535646,0.000039770024],"domain_scores_gemma":[0.9982823,0.0011487417,0.00022213983,0.00004001719,0.00023508848,0.00007169308],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0010763449,0.0007621577,0.0016466154,0.002588536,0.00019820857,0.001088416,0.0010981184,0.0015495052,0.002285222],"category_scores_gemma":[0.0031318092,0.0003200733,0.0008591097,0.0020379247,0.00056754693,0.0012598453,0.0008563665,0.0018683233,0.00068223366],"study_design_candidate":"meta_analysis","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00014079854,0.00003891365,0.0018082866,0.018368866,0.0004634145,0.00092288374,0.00007253793,0.000373516,0.0010967294,0.003826245,0.036794584,0.9360933],"study_design_scores_gemma":[0.00007082987,0.00009545418,0.0041882927,0.009621225,0.0013965097,0.006125713,0.000114644696,0.00021722277,0.00060844934,0.0054399725,0.97206074,0.000061057646],"about_ca_topic_score_codex":0.0013788306,"about_ca_topic_score_gemma":0.002048014,"teacher_disagreement_score":0.002588536,"about_ca_system_score_codex":0.00058899686,"about_ca_system_score_gemma":0.0014713276,"threshold_uncertainty_score":0.0076447725},"labels":[],"label_agreement":null},{"id":"W2903782905","doi":"10.1038/s41588-018-0303-9","title":"Trans-ethnic association study of blood pressure determinants in over 750,000 individuals","year":2018,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Genetic Associations and Epidemiology","field":"Biochemistry, Genetics and Molecular Biology","cited_by":501,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Université Laval; Population Health Research Institute; McMaster University","funders":"Institute of Genetics; Eunice Kennedy Shriver National Institute of Child Health and Human Development; National Institute of Arthritis and Musculoskeletal and Skin Diseases; National Institute of Diabetes and Digestive and Kidney Diseases; National Eye Institute; National Human Genome Research Institute; National Heart, Lung, and Blood Institute; NIHR Leicester Biomedical Research Centre; National Institutes of Health; University of Ioannina; National Cancer Institute; Servier; Novo Nordisk Fonden; Université de Bordeaux; Lunds Universitet; Vanderbilt University Medical Center; Universiteit Leiden; Hunter Medical Research Institute; European Commission; Medical Research Council; Leids Universitair Medisch Centrum; Department of Health and Social Care; National Institute on Aging; National Institute for Health and Care Research; Institut National de la Santé et de la Recherche Médicale; Menzies Centre for Australian Studies, King's College London, University of London; U.S. Department of Veterans Affairs; Government of the United Kingdom; University of Texas Health Science Center at Houston; Imperial College London; University of Dundee; National Institute of General Medical Sciences; Université Laval; National Center for Research Resources; Agence Nationale de la Recherche; Wellcome Trust; McMaster University; Vanderbilt University; National Institute of Neurological Disorders and Stroke; British Heart Foundation; Brigham and Women's Hospital; Pfizer; Rijksuniversiteit Groningen; University of Leicester; Economic and Social Research Council; Universitair Medisch Centrum Groningen; U.S. Department of Health and Human Services","keywords":"Blood pressure; Biology; Phenome; Transcriptome; Gene; Single-nucleotide polymorphism; Genome-wide association study; Genetic association; Pulse pressure; Genetics; Genetic architecture; Gene expression; Genome; Endocrinology; Genotype; Quantitative trait locus","score_opus":0.011650274438719396,"score_gpt":0.306612492019768,"score_spread":0.29496221758104857,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2903782905","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9982456,0.0003360424,0.00022375687,0.00006701065,0.000017864812,0.000007220653,0.0004877101,0.0000054937486,0.0006092252],"genre_scores_gemma":[0.9983975,0.00020119616,0.00021250751,0.000059990653,0.000016222219,0.0000114383165,0.00040494135,0.000006437988,0.0006897665],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99894494,0.00034368853,0.00013098211,0.0003069247,0.00014265743,0.00013080836],"domain_scores_gemma":[0.9985519,0.00020871431,0.00034224783,0.000273428,0.00027992018,0.00034368798],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0009292335,0.00042647347,0.00048929057,0.0007723531,0.0013050814,0.0008793486,0.0005529789,0.0006917327,0.0015537093],"category_scores_gemma":[0.0020274248,0.0005983083,0.00056319335,0.0027697086,0.00038931132,0.00058996317,0.0007415589,0.0010738494,0.00040889083],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0002241663,0.000063579835,0.99707806,0.0000097706325,0.00032449645,0.00016623725,0.00033554184,0.000027541479,0.00064138445,0.000050453607,0.00017327434,0.00090547575],"study_design_scores_gemma":[0.000015994969,0.00008036179,0.9982768,0.0000066354455,0.00016464766,0.00034218247,0.00048160777,0.0001233328,0.00007508551,0.000034605753,0.0003917449,0.0000069357266],"about_ca_topic_score_codex":0.039098002,"about_ca_topic_score_gemma":0.051319372,"teacher_disagreement_score":0.039098002,"about_ca_system_score_codex":0.00032961683,"about_ca_system_score_gemma":0.00052142155,"threshold_uncertainty_score":0.07774085},"labels":[],"label_agreement":null},{"id":"W2904039649","doi":"10.1038/s41588-018-0302-x","title":"An atlas of genetic influences on osteoporosis in humans and mice","year":2018,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Genetic Associations and Epidemiology","field":"Biochemistry, Genetics and Molecular Biology","cited_by":833,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"McGill Genome Centre; McGill University Health Centre; McGill University; McGill University and Génome Québec Innovation Centre; Jewish General Hospital","funders":"National Institute of Arthritis and Musculoskeletal and Skin Diseases; Diamantina Institute, University of Queensland; Engineering and Physical Sciences Research Council; Fonds de Recherche du Québec - Santé; Canadian Institutes of Health Research; National Institutes of Health; Medical Research Council; Australian Government; Versus Arthritis; National Health and Medical Research Council; Novo Nordisk Fonden; National Institute of General Medical Sciences; National Institute for Health and Care Research; Novo Nordisk; ZonMw; Sahlgrenska Universitetssjukhuset; Stiftelsen för Strategisk Forskning; European Commission; Vetenskapsrådet; British Heart Foundation; Wellcome Trust; Knut och Alice Wallenbergs Stiftelse; King's College London; Ernest Heine Family Foundation","keywords":"Biology; Genome-wide association study; Osteoporosis; Bone mineral; Bone density; Phenotype; Genetics; Quantitative trait locus; Single-nucleotide polymorphism; Epigenomics; Gene; Genetic association; Bioinformatics; Endocrinology; Gene expression; Genotype","score_opus":0.007560850109012619,"score_gpt":0.28508999624678166,"score_spread":0.277529146137769,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2904039649","genre_codex":"review","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":null,"domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.114961065,0.24076846,0.15649025,0.010485225,0.004135675,0.00042995313,0.22139964,0.028383438,0.22294635],"genre_scores_gemma":[0.26375672,0.3100409,0.16152452,0.0044498593,0.0023692036,0.00057353155,0.10824359,0.002447802,0.14659396],"study_design_codex":"design_other","study_design_gemma":"observational","domain_scores_codex":[0.99980897,0.000036935147,0.000017658347,0.000037470167,0.00007211826,0.000026872916],"domain_scores_gemma":[0.99941313,0.00019328983,0.000104775136,0.00007340948,0.00011286783,0.00010264939],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00027774667,0.0005587073,0.0004221711,0.0062862905,0.00031392786,0.0007467004,0.0003781228,0.00037491854,0.016495507],"category_scores_gemma":[0.0006033056,0.00028470953,0.00047869407,0.0049961056,0.00023822852,0.0004697785,0.0005619245,0.00063997076,0.0026102208],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00067541783,0.00008742127,0.014937311,0.002836695,0.0004479167,0.0017170215,0.00035824982,0.004317147,0.08080909,0.029460806,0.26996785,0.5943851],"study_design_scores_gemma":[0.000042740354,0.00011797615,0.07847079,0.00036933512,0.00025416614,0.0035225924,0.00012829904,0.0010481429,0.0050768135,0.015092222,0.8958291,0.000047891677],"about_ca_topic_score_codex":0.004125492,"about_ca_topic_score_gemma":0.0097167,"teacher_disagreement_score":0.016495507,"about_ca_system_score_codex":0.00051803875,"about_ca_system_score_gemma":0.00072544004,"threshold_uncertainty_score":0.055182934},"labels":[],"label_agreement":null},{"id":"W2908002252","doi":"10.1038/s41588-018-0311-9","title":"Genome-wide meta-analysis identifies new loci and functional pathways influencing Alzheimer’s disease risk","year":2019,"lang":"en","type":"review","venue":"Nature Genetics","topic":"Genetic Associations and Epidemiology","field":"Biochemistry, Genetics and Molecular Biology","cited_by":2526,"is_retracted":false,"has_abstract":false,"route_ca_aff":false,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"","funders":"National Institute of Neurological Disorders and Stroke; National Institute on Deafness and Other Communication Disorders; National Institute of Mental Health; National Heart, Lung, and Blood Institute; Medical Research Council; National Institute of General Medical Sciences; Centre hospitalier régional universitaire de Lille; Nasjonalforeningen for Folkehelsen; Karl-Franzens-Universität Graz; Vrije Universiteit Amsterdam; Erasmus Medisch Centrum; Norges Forskningsråd; Hjartavernd; National Institutes of Health; Österreichische Forschungsförderungsgesellschaft; Austrian Science Fund; EU Joint Programme – Neurodegenerative Disease Research; Institut National de la Santé et de la Recherche Médicale; Université de Lille; European Commission; Medizinische Universität Graz; Oesterreichische Nationalbank; Alzheimer's Association; University of Toronto; Case Western Reserve University; European Federation of Pharmaceutical Industries and Associations; Bundesministerium für Bildung und Forschung; National Institute on Aging; National Institute for Health and Care Research; Nederlandse Organisatie voor Wetenschappelijk Onderzoek; Wellcome Trust; Development of Innovative Strategies for a Transdisciplinary approach to ALZheimer's disease","keywords":"Biology; Mendelian randomization; Genome-wide association study; Disease; Genetics; Alzheimer's disease; Genetic association; TREM2; Gene; Genome; Single-nucleotide polymorphism; Immune system; Genetic variants; Genotype; Medicine; Internal medicine","score_opus":0.07306734977297584,"score_gpt":0.3208350366448556,"score_spread":0.24776768687187972,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2908002252","genre_codex":"review","genre_gemma":"review","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"review","genre_consensus":"review","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.0004288622,0.99723357,0.0005525351,0.0010888791,0.00023426974,0.000004023115,0.00018174872,0.000015181352,0.00026098563],"genre_scores_gemma":[0.0046886466,0.9922984,0.0009369386,0.00089560583,0.0006537777,0.000014011347,0.0002792119,0.000006700833,0.00022672748],"study_design_codex":"design_other","study_design_gemma":"meta_analysis","domain_scores_codex":[0.99925107,0.0002600416,0.00009946254,0.00019876986,0.00014445778,0.00004614502],"domain_scores_gemma":[0.99729615,0.0020428905,0.00023158322,0.00010139134,0.00024057295,0.00008734564],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0032248178,0.0015042387,0.003219491,0.001713513,0.00015020749,0.0013233721,0.001471954,0.0014862226,0.0021372326],"category_scores_gemma":[0.003988776,0.0004173136,0.0021919361,0.0028085061,0.00042628447,0.00064705743,0.0009232369,0.0018620127,0.0005505497],"study_design_candidate":"meta_analysis","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.001058291,0.00006199508,0.0097494945,0.028118076,0.01795317,0.000453538,0.00005465232,0.0010171444,0.0012515655,0.003532375,0.037313845,0.89943594],"study_design_scores_gemma":[0.0010915835,0.00066606863,0.08635904,0.033824574,0.07585552,0.0048388927,0.00028402644,0.0018412016,0.0018531696,0.036416538,0.7566542,0.0003152548],"about_ca_topic_score_codex":0.002350259,"about_ca_topic_score_gemma":0.0056418846,"teacher_disagreement_score":0.0032248178,"about_ca_system_score_codex":0.00063101546,"about_ca_system_score_gemma":0.0016627326,"threshold_uncertainty_score":0},"labels":[],"label_agreement":null},{"id":"W2908554893","doi":"10.1038/s41588-018-0330-6","title":"Author Correction: Association analyses of more than 140,000 men identify 63 new prostate cancer susceptibility loci","year":2019,"lang":"en","type":"erratum","venue":"Nature Genetics","topic":"Prostate Cancer Treatment and Research","field":"Medicine","cited_by":24,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Alberta; Princess Margaret Cancer Centre","funders":"Medical Research Council; National Institute for Health and Care Research; Cancer Research UK","keywords":"Biology; Prostate cancer; Association (psychology); Computational biology; Genetics; Cancer; Psychology","score_opus":0.03662744868537579,"score_gpt":0.41180633990927934,"score_spread":0.3751788912239036,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2908554893","genre_codex":"editorial","genre_gemma":"other","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"other","genre_consensus":null,"domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.00015582373,0.0004734828,0.00064742117,0.03385666,0.9620921,0.000016674927,0.0012195739,0.0003103317,0.0012279301],"genre_scores_gemma":[0.023455815,0.0055336365,0.010609204,0.15131374,0.508784,0.00032844685,0.006493695,0.0040120124,0.28946945],"study_design_codex":"not_applicable","study_design_gemma":"not_applicable","domain_scores_codex":[0.99383837,0.0010074135,0.0010224526,0.0010600418,0.0024776934,0.00059412036],"domain_scores_gemma":[0.95793796,0.011008067,0.0023563786,0.003108541,0.023328248,0.002260771],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0059560924,0.0027160638,0.0023223239,0.0042397184,0.0036425567,0.004235079,0.0047280258,0.007959532,0.08450324],"category_scores_gemma":[0.078375205,0.0017404958,0.0021950922,0.0025160704,0.0021830457,0.0020726428,0.0023485795,0.013236268,0.03403755],"study_design_candidate":"not_applicable","study_design_consensus":"not_applicable","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.000034582175,0.0000052667565,0.000118637436,0.00008354123,0.0000216553,0.0002870124,0.000018278595,0.00002853937,0.000033145297,0.00026518124,0.9968035,0.0023007297],"study_design_scores_gemma":[0.0002215173,0.000034462035,0.0018176142,0.00059679657,0.00018812934,0.0018877444,0.0001250592,0.00050351635,0.0005881338,0.0021304912,0.9918298,0.0000766822],"about_ca_topic_score_codex":0.023976827,"about_ca_topic_score_gemma":0.03196185,"teacher_disagreement_score":0.08450324,"about_ca_system_score_codex":0.0041986057,"about_ca_system_score_gemma":0.0063662147,"threshold_uncertainty_score":0.28269148},"labels":[],"label_agreement":null},{"id":"W2908755714","doi":"10.1038/s41588-018-0318-2","title":"Molecular landmarks of tumor hypoxia across cancer types","year":2019,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Cancer, Hypoxia, and Metabolism","field":"Biochemistry, Genetics and Molecular Biology","cited_by":717,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Princess Margaret Cancer Centre; University of Toronto; University Health Network; Health Sciences Centre; Sunnybrook Health Science Centre; Ontario Institute for Cancer Research","funders":"","keywords":"Biology; Hypoxia (environmental); PTEN; Tumor hypoxia; Cancer research; Metastasis; Genome instability; microRNA; Cancer; Tumor progression; Prostate cancer; Chromosome instability; Tumor microenvironment; Pathology; Internal medicine; Gene; Genetics; Apoptosis; DNA damage; Tumor cells; PI3K/AKT/mTOR pathway; DNA; Medicine","score_opus":0.004033118511278832,"score_gpt":0.2642381032104693,"score_spread":0.26020498469919046,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2908755714","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9720686,0.0072479863,0.009551653,0.0012283227,0.00007599324,0.000029501922,0.0010507884,0.0001925171,0.008554701],"genre_scores_gemma":[0.99483806,0.0015611753,0.0013338326,0.00012586427,0.0000243512,0.000018476949,0.00037007683,0.000029657618,0.0016985133],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9998884,0.000014882889,0.000006875333,0.000028713632,0.000025259345,0.00003577268],"domain_scores_gemma":[0.99970394,0.000042642107,0.00010895691,0.000028078926,0.000051608662,0.000064724976],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00015597463,0.00012187531,0.00023128053,0.00091263634,0.00031868453,0.00068170985,0.00027856615,0.0003163977,0.0020139387],"category_scores_gemma":[0.00025523992,0.00022305835,0.00015286772,0.00048691887,0.00033954528,0.00044337398,0.00046061116,0.0005486957,0.00027186572],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00070134795,0.000025965423,0.014992771,0.000095350035,0.00003992096,0.00027275173,0.00015858341,0.00046340754,0.95935446,0.010669556,0.0005974098,0.012628455],"study_design_scores_gemma":[0.00005465586,0.0005455075,0.48855007,0.000058122296,0.00016656541,0.0030540798,0.0010423035,0.0022565613,0.46823084,0.0104621705,0.02552522,0.000053859225],"about_ca_topic_score_codex":0.0013935454,"about_ca_topic_score_gemma":0.0015842612,"teacher_disagreement_score":0.0020139387,"about_ca_system_score_codex":0.00040516764,"about_ca_system_score_gemma":0.00026096133,"threshold_uncertainty_score":0.0067373514},"labels":[],"label_agreement":null},{"id":"W2909486692","doi":"10.1038/s41588-018-0309-3","title":"Genome-wide association analyses of risk tolerance and risky behaviors in over 1 million individuals identify hundreds of loci and shared genetic influences","year":2019,"lang":"en","type":"review","venue":"Nature Genetics","topic":"Genetic Associations and Epidemiology","field":"Biochemistry, Genetics and Molecular Biology","cited_by":841,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"St. Joseph’s Healthcare Hamilton; Homewood Research Institute; Centre for Global Health Research; McMaster University; University of Toronto","funders":"National Institute on Aging; Biotechnology and Biological Sciences Research Council; Medical Research Council; Social Sciences and Humanities Research Council of Canada; Vetenskapsrådet; Lundbeckfonden; Novo Nordisk Fonden; Cancer Research UK; Government of Canada; Open Philanthropy Project; National Institute for Health and Care Research; Genome Canada; Wellcome Trust; Nederlandse Organisatie voor Wetenschappelijk Onderzoek; University of Southern California; National Institutes of Health; Ontario Genomics; Ontario Genomics Institute; Eunice Kennedy Shriver National Institute of Child Health and Human Development; Economic and Social Research Council; Sanofi","keywords":"Biology; Genome-wide association study; Genetics; Association (psychology); Genetic association; Evolutionary biology; Single-nucleotide polymorphism; Genotype; Gene","score_opus":0.025916163810383884,"score_gpt":0.3624713575839626,"score_spread":0.33655519377357873,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2909486692","genre_codex":"review","genre_gemma":"review","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"review","genre_consensus":"review","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.00009066918,0.997835,0.00029515172,0.00093313033,0.00033145107,0.0000029415555,0.000056897326,0.000010330456,0.00044446188],"genre_scores_gemma":[0.00058360776,0.9973029,0.00040341637,0.0006008331,0.000566663,0.000006684481,0.00007888553,0.00000237794,0.00045464118],"study_design_codex":"design_other","study_design_gemma":"observational","domain_scores_codex":[0.99955636,0.00009912197,0.000060852868,0.0001100944,0.00014235974,0.00003116567],"domain_scores_gemma":[0.9982065,0.0011830385,0.00016234518,0.00004578462,0.00027996564,0.00012238914],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0018815114,0.0014711111,0.0021575708,0.001840348,0.00022215651,0.0012859863,0.0013795247,0.0020081096,0.0028178415],"category_scores_gemma":[0.0024176121,0.0003674242,0.0006957286,0.0022505533,0.0007558816,0.0009725851,0.0011239493,0.0025809803,0.0015367351],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00013244944,0.00004245034,0.0013803892,0.0060309423,0.00037982175,0.00013888818,0.000028102817,0.00024004157,0.0005299276,0.0030304797,0.034890033,0.9531765],"study_design_scores_gemma":[0.000103178645,0.00013237716,0.011062477,0.009015925,0.00097095885,0.0014601544,0.0001097755,0.00023819324,0.0003767731,0.010386876,0.9660642,0.000078988814],"about_ca_topic_score_codex":0.0029268085,"about_ca_topic_score_gemma":0.005134837,"teacher_disagreement_score":0.0029268085,"about_ca_system_score_codex":0.00064131984,"about_ca_system_score_gemma":0.0015951571,"threshold_uncertainty_score":0.009950519},"labels":[],"label_agreement":null},{"id":"W2909547032","doi":"10.1038/s41588-018-0315-5","title":"PAX5-driven subtypes of B-progenitor acute lymphoblastic leukemia","year":2019,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Acute Lymphoblastic Leukemia research","field":"Medicine","cited_by":617,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Princess Margaret Cancer Centre; University Health Network","funders":"National Institute of General Medical Sciences; National Cancer Institute","keywords":"Biology; Lymphoblastic Leukemia; Progenitor; Progenitor cell; Cancer research; Computational biology; Leukemia; Genetics; Immunology; Stem cell","score_opus":0.007594102956109199,"score_gpt":0.27520868129986936,"score_spread":0.2676145783437602,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2909547032","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9822183,0.0011828829,0.0019586708,0.00020319683,0.000024653558,0.000075263684,0.0011211892,0.00015238055,0.013063411],"genre_scores_gemma":[0.9943515,0.00036477912,0.0007182516,0.00009270318,0.0000073990627,0.00002992996,0.0011188843,0.00004246832,0.003274059],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9996846,0.000047408736,0.00002435912,0.000048787773,0.00010153022,0.00009343015],"domain_scores_gemma":[0.99984574,0.000027359709,0.00003704654,0.000031438864,0.000011096869,0.000047278252],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00021179911,0.00021516513,0.00018374917,0.00063509797,0.00039243366,0.0009627806,0.00039500467,0.00035841257,0.005389092],"category_scores_gemma":[0.00026522373,0.00018445749,0.00020244556,0.0004062945,0.0002688453,0.0003358622,0.0008586265,0.0007654119,0.0008214375],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0013109038,0.0002390624,0.055949606,0.00023511852,0.0000998943,0.003401523,0.00048947445,0.0010761723,0.8734544,0.028549105,0.0038647994,0.03132998],"study_design_scores_gemma":[0.0003083622,0.0010517382,0.29038307,0.00012093727,0.00027502025,0.054662764,0.0021824792,0.007874828,0.5034421,0.010665067,0.1289818,0.00005179222],"about_ca_topic_score_codex":0.0010120411,"about_ca_topic_score_gemma":0.0023613675,"teacher_disagreement_score":0.005389092,"about_ca_system_score_codex":0.000729325,"about_ca_system_score_gemma":0.00031681455,"threshold_uncertainty_score":0.018028319},"labels":[],"label_agreement":null},{"id":"W2916398036","doi":"10.1038/s41588-019-0354-6","title":"Doubts about TMEM230 as a gene for parkinsonism","year":2019,"lang":"en","type":"letter","venue":"Nature Genetics","topic":"Neurogenetic and Muscular Disorders Research","field":"Medicine","cited_by":18,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of British Columbia; University of British Columbia Hospital","funders":"","keywords":"Biology; Parkinsonism; Genetics; Gene; Computational biology; Disease; Internal medicine","score_opus":0.018964330277098766,"score_gpt":0.3279888085651645,"score_spread":0.30902447828806573,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2916398036","genre_codex":"commentary","genre_gemma":"commentary","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"commentary","genre_consensus":"commentary","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.0025854583,0.0015104918,0.00008275241,0.9799888,0.012214081,0.0000053392837,0.00003543382,0.000015195761,0.0035624513],"genre_scores_gemma":[0.06185648,0.0023943097,0.00033864134,0.83447593,0.09180112,0.0000280504,0.00006478582,0.000051070638,0.008989603],"study_design_codex":"not_applicable","study_design_gemma":"theoretical_or_conceptual","domain_scores_codex":[0.99805367,0.00058988435,0.00025534892,0.0003045565,0.0004098158,0.00038684788],"domain_scores_gemma":[0.98923665,0.007267565,0.00062213745,0.00037659463,0.0011160477,0.0013809688],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0026243762,0.00068535155,0.0013158076,0.0011230401,0.0044398564,0.0029727847,0.0016447799,0.06357757,0.0073052538],"category_scores_gemma":[0.027565202,0.0008255698,0.0012597955,0.00072270003,0.004223139,0.0036183815,0.0017692056,0.03034806,0.0045130244],"study_design_candidate":"theoretical_or_conceptual","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0003692917,0.00009574309,0.005408543,0.00013853339,0.000093680705,0.10089656,0.0010356221,0.00021652222,0.0014324443,0.014682597,0.85564995,0.019980617],"study_design_scores_gemma":[0.00077962445,0.00037965513,0.0068232846,0.0013894439,0.00032115774,0.14924169,0.003054166,0.0031315559,0.0017280956,0.11267476,0.72019684,0.00027976956],"about_ca_topic_score_codex":0.0036362058,"about_ca_topic_score_gemma":0.003425127,"teacher_disagreement_score":0.06357757,"about_ca_system_score_codex":0.004374363,"about_ca_system_score_gemma":0.0029883021,"threshold_uncertainty_score":0.0317384},"labels":[],"label_agreement":null},{"id":"W2916749909","doi":"10.1038/s41588-019-0358-2","title":"Genetic meta-analysis of diagnosed Alzheimer’s disease identifies new risk loci and implicates Aβ, tau, immunity and lipid processing","year":2019,"lang":"en","type":"review","venue":"Nature Genetics","topic":"Alzheimer's disease research and treatments","field":"Medicine","cited_by":3204,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Occupational Cancer Research Centre; University of Toronto","funders":"National Heart, Lung, and Blood Institute; National Institute on Aging; National Institute of Neurological Disorders and Stroke; Medical Research Council; Agence Nationale de la Recherche; National Center for Advancing Translational Sciences; Rosetrees Trust; Motor Neurone Disease Association; Parkinson's UK; National Institute for Health and Care Research; Wellcome Trust","keywords":"Biology; Immunity; Disease; Genetics; Alzheimer's disease; Meta-analysis; Bioinformatics; Evolutionary biology; Computational biology; Immune system; Internal medicine","score_opus":0.10164479276214171,"score_gpt":0.40206656319146117,"score_spread":0.30042177042931945,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2916749909","genre_codex":"review","genre_gemma":"review","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"review","genre_consensus":"review","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.00047822256,0.9988193,0.0001636543,0.00018552883,0.00009901884,0.0000058528435,0.00010262862,0.0000075113167,0.00013828641],"genre_scores_gemma":[0.010267647,0.9878209,0.0006634455,0.0005730583,0.00023474851,0.000020670037,0.00022786438,0.000006252389,0.00018529201],"study_design_codex":"design_other","study_design_gemma":"meta_analysis","domain_scores_codex":[0.9992729,0.00026842134,0.00015232788,0.00015079505,0.00011669174,0.000038835366],"domain_scores_gemma":[0.99761945,0.001809199,0.00028554167,0.00007286345,0.00016749366,0.00004546773],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0024570543,0.0013385874,0.00463052,0.0012948662,0.00013845989,0.0008072143,0.0012142563,0.00095521985,0.002928944],"category_scores_gemma":[0.0045284643,0.00047849584,0.00453547,0.0017527739,0.00021719189,0.0004673619,0.0006703422,0.0010275578,0.00036052355],"study_design_candidate":"meta_analysis","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0026046159,0.00007357311,0.0076853544,0.21342808,0.1470024,0.00039918823,0.000091853486,0.0010596089,0.0011451795,0.0020209262,0.019922553,0.60456663],"study_design_scores_gemma":[0.0025569585,0.0010311498,0.05317649,0.07680005,0.58963674,0.002493659,0.00019555145,0.0009719393,0.0011477238,0.0126247965,0.25912258,0.00024226312],"about_ca_topic_score_codex":0.0034584438,"about_ca_topic_score_gemma":0.009123754,"teacher_disagreement_score":0.00463052,"about_ca_system_score_codex":0.00065028644,"about_ca_system_score_gemma":0.0014814931,"threshold_uncertainty_score":0.012994289},"labels":[],"label_agreement":null},{"id":"W2917263971","doi":"10.1038/s41588-018-0342-2","title":"Genetic landscape of chronic obstructive pulmonary disease identifies heterogeneous cell-type and phenotype associations","year":2019,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Chronic Obstructive Pulmonary Disease (COPD) Research","field":"Medicine","cited_by":423,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Université Laval; St. Paul's Hospital; University of British Columbia; Institut universitaire de cardiologie et de pneumologie de Québec","funders":"Biotechnology and Biological Sciences Research Council; National Heart, Lung, and Blood Institute; Medical Research Council; National Institute for Health and Care Research; Wellcome Trust","keywords":"Biology; Phenotype; Pulmonary disease; Genetics; Disease; Genetic heterogeneity; Evolutionary biology; Gene; Internal medicine; Medicine","score_opus":0.007434365858327551,"score_gpt":0.2635679386085148,"score_spread":0.2561335727501872,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2917263971","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9966259,0.00062239316,0.0010094802,0.00020470875,0.00002190169,0.000009761052,0.00052202196,0.000018854687,0.00096492236],"genre_scores_gemma":[0.99851304,0.00019938922,0.0004095468,0.00013182432,0.000028917668,0.000009421098,0.0003231984,0.000029491897,0.00035513667],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99916553,0.00022491644,0.00006129318,0.0002718394,0.0001457731,0.00013058992],"domain_scores_gemma":[0.9989042,0.00047614318,0.00027713564,0.000120612916,0.000107643464,0.000114226474],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0004736994,0.00034887673,0.0006025508,0.0013500083,0.00039793758,0.0010084761,0.00039155787,0.0007222146,0.0031996456],"category_scores_gemma":[0.0019899094,0.00021173693,0.00042703547,0.0011443419,0.00044288248,0.0003827085,0.0006790273,0.00060847105,0.00035983662],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0012017796,0.00012468157,0.7708269,0.00009719011,0.0005861275,0.0017645981,0.0005728404,0.00059109984,0.20399433,0.0013315892,0.0009813833,0.017927533],"study_design_scores_gemma":[0.0000231034,0.00011589615,0.9909401,0.000022836633,0.00017222737,0.0017733978,0.00027888746,0.00093324285,0.0031686453,0.0014562289,0.0010941965,0.000021192018],"about_ca_topic_score_codex":0.0010768761,"about_ca_topic_score_gemma":0.0014878382,"teacher_disagreement_score":0.0031996456,"about_ca_system_score_codex":0.0001829049,"about_ca_system_score_gemma":0.0001608328,"threshold_uncertainty_score":0.010703862},"labels":[],"label_agreement":null},{"id":"W2931575838","doi":"10.1038/s41588-019-0381-3","title":"Durum wheat genome highlights past domestication signatures and future improvement targets","year":2019,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Wheat and Barley Genetics and Pathology","field":"Agricultural and Biological Sciences","cited_by":824,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Agriculture and Agri-Food Canada; Global Institute for Water Security; University of Saskatchewan; University of Alberta","funders":"FP7 Food, Agriculture and Fisheries, Biotechnology; Saskatchewan Wheat Development Commission; Genome Prairie; Bundesministerium für Ernährung und Landwirtschaft; University of Alberta; Ministry of Agriculture - Saskatchewan; Agricultural Research Service; Genome Canada; North Dakota State University; U.S. Department of Agriculture","keywords":"Domestication; Biology; Genome; Genetic diversity; Cultivar; Locus (genetics); Genetics; Allele; Gene; Botany; Population","score_opus":0.00436200584650663,"score_gpt":0.19995223326908856,"score_spread":0.19559022742258195,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2931575838","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.97372174,0.006550816,0.0047367415,0.00047366077,0.000044526216,0.000010301929,0.010081844,0.00026772122,0.0041125705],"genre_scores_gemma":[0.9634238,0.0025713418,0.00732027,0.00020176679,0.000031576175,0.000009092793,0.024010506,0.000101000405,0.0023306026],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9999417,0.0000037896189,0.0000032549262,0.00003160705,0.000009056193,0.000010588125],"domain_scores_gemma":[0.9999236,0.000014446617,0.00001963719,0.0000091786615,0.000011469246,0.00002170958],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00010229058,0.00022961485,0.00029702787,0.00034979606,0.00020592434,0.0004116766,0.00010982074,0.00019666078,0.0010062822],"category_scores_gemma":[0.00012554218,0.00010091569,0.00018493984,0.0006828715,0.00009052289,0.00019358548,0.00023003054,0.00035183266,0.00025361683],"study_design_candidate":"bench_or_experimental","study_design_consensus":"bench_or_experimental","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00062303216,0.00003345664,0.029585803,0.0004099856,0.00007812022,0.00081749837,0.00045005788,0.00056289806,0.9107713,0.0009154544,0.0012682758,0.054484066],"study_design_scores_gemma":[0.00003878187,0.00019810798,0.8367903,0.00010452786,0.00021217027,0.0020376807,0.00056693214,0.0021628812,0.06351763,0.0020080304,0.09233121,0.00003163618],"about_ca_topic_score_codex":0.0014352198,"about_ca_topic_score_gemma":0.003949252,"teacher_disagreement_score":0.0014352198,"about_ca_system_score_codex":0.00023255196,"about_ca_system_score_gemma":0.00012305101,"threshold_uncertainty_score":0.0033663511},"labels":[],"label_agreement":null},{"id":"W2937995944","doi":"10.1038/s41588-019-0415-x","title":"Author Correction: An atlas of genetic influences on osteoporosis in humans and mice","year":2019,"lang":"en","type":"erratum","venue":"Nature Genetics","topic":"RNA Research and Splicing","field":"Biochemistry, Genetics and Molecular Biology","cited_by":22,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"McGill Genome Centre; McGill University Health Centre; McGill University; McGill University and Génome Québec Innovation Centre; Jewish General Hospital","funders":"Versus Arthritis; Engineering and Physical Sciences Research Council; Novo Nordisk Fonden; Medical Research Council; National Institute for Health and Care Research","keywords":"Biology; Atlas (anatomy); Column (typography); Computational biology; Genetics; Statistics; Internal medicine; Anatomy; Mathematics; Medicine; Geometry","score_opus":0.009732835735908886,"score_gpt":0.2960310780123045,"score_spread":0.2862982422763956,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2937995944","genre_codex":"editorial","genre_gemma":"other","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"other","genre_consensus":null,"domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.00047236393,0.0027144628,0.003978288,0.030549508,0.94009954,0.000048685088,0.0074782684,0.001654657,0.013004215],"genre_scores_gemma":[0.017361315,0.014277901,0.024621585,0.032729,0.18489352,0.00039118447,0.016089771,0.0062521454,0.70338356],"study_design_codex":"not_applicable","study_design_gemma":"not_applicable","domain_scores_codex":[0.9976712,0.0003105234,0.00031292305,0.00030144787,0.0012291117,0.00017475872],"domain_scores_gemma":[0.98722804,0.002478833,0.0006554282,0.0010743963,0.007819438,0.0007438237],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0023329286,0.0015893597,0.0012736219,0.005137851,0.0018718267,0.0025270286,0.0023487972,0.002629217,0.10896254],"category_scores_gemma":[0.018221896,0.00071298156,0.0012397191,0.0029719337,0.0011726856,0.0013139122,0.0015215724,0.0047787926,0.03685823],"study_design_candidate":"not_applicable","study_design_consensus":"not_applicable","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00003739494,0.0000036591077,0.00007836958,0.00012746565,0.000011566274,0.00019785581,0.000012849338,0.000049261856,0.0001220952,0.00085886964,0.98791647,0.010584275],"study_design_scores_gemma":[0.000024736457,0.000009491251,0.0005207164,0.0001364247,0.000033744334,0.0006081412,0.000022465372,0.00011789348,0.0005165779,0.0010670625,0.996926,0.00001661955],"about_ca_topic_score_codex":0.0101071615,"about_ca_topic_score_gemma":0.021760581,"teacher_disagreement_score":0.10896254,"about_ca_system_score_codex":0.0024997864,"about_ca_system_score_gemma":0.0038181143,"threshold_uncertainty_score":0.36451602},"labels":[],"label_agreement":null},{"id":"W2942952616","doi":"10.1038/s41588-019-0399-6","title":"Ongoing chromosomal instability and karyotype evolution in human colorectal cancer organoids","year":2019,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Cancer Genomics and Diagnostics","field":"Biochemistry, Genetics and Molecular Biology","cited_by":244,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"BC Cancer Agency","funders":"","keywords":"Chromosome instability; Biology; Aneuploidy; Karyotype; Microsatellite instability; Colorectal cancer; Genome instability; Organoid; Mitosis; Cancer research; Cancer; Genetic heterogeneity; Genetics; Chromosome; Phenotype; Gene; DNA damage; DNA; Microsatellite","score_opus":0.003224133664508974,"score_gpt":0.24005448607791433,"score_spread":0.23683035241340536,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2942952616","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99642795,0.00068399374,0.0011366248,0.000042627355,0.00000551896,0.0000073120755,0.0006710066,0.000038860242,0.0009861137],"genre_scores_gemma":[0.9966126,0.00039375303,0.0005385521,0.000022840733,0.000002180319,0.000010859901,0.0009996203,0.000022178338,0.0013974083],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9998708,0.000019978044,0.000014388766,0.000034465742,0.000035086377,0.000025256948],"domain_scores_gemma":[0.99974424,0.00006937941,0.000047521928,0.000053944594,0.00004313835,0.000041722575],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00016613523,0.0001205712,0.00020569572,0.00060165185,0.00030646625,0.0004873094,0.0001506951,0.00023096341,0.001538164],"category_scores_gemma":[0.00038379728,0.00015595499,0.00023164932,0.00045712086,0.00016302949,0.00018699515,0.00040025247,0.00029475417,0.00038333764],"study_design_candidate":"bench_or_experimental","study_design_consensus":"bench_or_experimental","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00025339087,0.000005590046,0.0054815225,0.000020803558,0.000012283244,0.00015787085,0.00013174221,0.00023402486,0.9899075,0.00014727579,0.000055444205,0.0035926718],"study_design_scores_gemma":[0.000023518842,0.00047765163,0.40120018,0.000022056496,0.000093574825,0.0034246221,0.00079898734,0.0028794762,0.5776349,0.00038565564,0.013018395,0.000040986888],"about_ca_topic_score_codex":0.003476192,"about_ca_topic_score_gemma":0.0041338108,"teacher_disagreement_score":0.003476192,"about_ca_system_score_codex":0.00041215424,"about_ca_system_score_gemma":0.00022773714,"threshold_uncertainty_score":0.0069119334},"labels":[],"label_agreement":null},{"id":"W2943169182","doi":"10.1038/s41588-019-0398-7","title":"SETD2 regulates the maternal epigenome, genomic imprinting and embryonic development","year":2019,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Epigenetics and DNA Methylation","field":"Biochemistry, Genetics and Molecular Biology","cited_by":279,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of British Columbia","funders":"Canadian Institutes of Health Research; Tsinghua University","keywords":"Epigenome; Biology; H3K4me3; Genomic imprinting; DNA methylation; Oocyte; Cell biology; Genetics; Epigenetics; Histone methylation; Histone H3; Chromatin; Embryo; Gene","score_opus":0.00424101838882649,"score_gpt":0.2258793797423996,"score_spread":0.22163836135357312,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2943169182","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.93515056,0.0151775405,0.020440793,0.0011777561,0.00036943596,0.00003374046,0.002585685,0.0005492592,0.024515286],"genre_scores_gemma":[0.98468715,0.0020240364,0.002685703,0.00017076138,0.000032197273,0.000019950563,0.0011487015,0.00008655392,0.009144933],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9998554,0.000017151226,0.0000068960403,0.000033521694,0.000055888646,0.000031147178],"domain_scores_gemma":[0.9998833,0.000021638574,0.000028261047,0.0000128469765,0.000014303382,0.000039698858],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0001303899,0.00037848196,0.00022404181,0.00034650275,0.00029448085,0.00074256444,0.00049968105,0.00036620427,0.0021908297],"category_scores_gemma":[0.00018925055,0.00026462838,0.00020484373,0.00020965649,0.00037261302,0.00032023143,0.00064190227,0.0005294641,0.00050785777],"study_design_candidate":"bench_or_experimental","study_design_consensus":"bench_or_experimental","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00022535502,0.000012303314,0.0017582597,0.000050126364,0.000015939842,0.00019233621,0.000027117172,0.00026010087,0.9893544,0.002457973,0.00043132884,0.005214811],"study_design_scores_gemma":[0.00003349513,0.00006719869,0.034020565,0.000016359256,0.000028880992,0.00074774947,0.00009515494,0.003405474,0.94357836,0.0012775821,0.016706696,0.000022369964],"about_ca_topic_score_codex":0.0007597611,"about_ca_topic_score_gemma":0.002098885,"teacher_disagreement_score":0.0021908297,"about_ca_system_score_codex":0.00066508213,"about_ca_system_score_gemma":0.00024664216,"threshold_uncertainty_score":0.0073290467},"labels":[],"label_agreement":null},{"id":"W2943467424","doi":"10.1038/s41588-019-0382-2","title":"Exome sequencing highlights the role of wild-relative introgression in shaping the adaptive landscape of the wheat genome","year":2019,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Wheat and Barley Genetics and Pathology","field":"Agricultural and Biological Sciences","cited_by":391,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Millar College of the Bible; University of Saskatchewan","funders":"","keywords":"Biology; Introgression; Exome sequencing; Exome; Genome; Evolutionary biology; Genetics; Adaptive evolution; DNA sequencing; Computational biology; Gene; Mutation","score_opus":0.012368918299333868,"score_gpt":0.21172163536945343,"score_spread":0.19935271707011956,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2943467424","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.96148914,0.0020986847,0.0236849,0.0011947833,0.00018896825,0.000021445578,0.0039790273,0.00024750238,0.0070954054],"genre_scores_gemma":[0.9868045,0.0010224744,0.005528802,0.0009683903,0.00007061727,0.000016096114,0.0024301733,0.00014881766,0.0030102462],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9995572,0.00004349924,0.00002249457,0.00025549618,0.000066864966,0.000054406784],"domain_scores_gemma":[0.99929476,0.00033986385,0.000102647806,0.00011850428,0.00006824938,0.000075958254],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00081149966,0.00035795107,0.00045639963,0.0005719605,0.00046703813,0.0012648562,0.00036236114,0.0009256362,0.003836682],"category_scores_gemma":[0.0012920451,0.00021550307,0.00038353374,0.0007947785,0.00052737456,0.0013549333,0.0009923498,0.0013080686,0.00061065226],"study_design_candidate":"bench_or_experimental","study_design_consensus":"bench_or_experimental","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0003753746,0.000050759398,0.0581,0.00030932087,0.00035958618,0.0010003119,0.0006488413,0.0017125916,0.87617445,0.006070509,0.0012137133,0.053984504],"study_design_scores_gemma":[0.000050700826,0.0002841918,0.8677221,0.00013955134,0.0003447462,0.003069825,0.0008153394,0.007574514,0.062247965,0.017429916,0.040187106,0.0001341586],"about_ca_topic_score_codex":0.0008813239,"about_ca_topic_score_gemma":0.0026474004,"teacher_disagreement_score":0.003836682,"about_ca_system_score_codex":0.00032439566,"about_ca_system_score_gemma":0.00022652527,"threshold_uncertainty_score":0.012835026},"labels":[],"label_agreement":null},{"id":"W2945671922","doi":"10.1038/s41588-019-0411-1","title":"Similarity regression predicts evolution of transcription factor sequence specificity","year":2019,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Genomics and Chromatin Dynamics","field":"Biochemistry, Genetics and Molecular Biology","cited_by":159,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Baker Hughes (Canada); Vector Institute; Canadian Institute for Advanced Research; Institute of Cancer Research; Ontario Institute for Cancer Research; Centre for Global Health Research; University of Toronto","funders":"","keywords":"Biology; Sequence motif; Computational biology; Motif (music); Transcription factor; Genetics; Gene; Zinc finger; DNA binding site; Genome; Evolutionary biology; Conserved sequence; Regression; Promoter; Gene expression; Peptide sequence","score_opus":0.009157682018527683,"score_gpt":0.24097422759526307,"score_spread":0.2318165455767354,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2945671922","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9800638,0.00020781592,0.017121553,0.00015765551,0.000014476991,0.000009571646,0.00020274724,0.00035666215,0.0018656669],"genre_scores_gemma":[0.9971733,0.000047079004,0.0020097897,0.00004269648,0.000013329284,0.0000045292813,0.00021637371,0.00006640577,0.00042651393],"study_design_codex":"bench_or_experimental","study_design_gemma":"simulation_or_modeling","domain_scores_codex":[0.9994481,0.0001291135,0.000021301199,0.00023844372,0.000095800526,0.00006723287],"domain_scores_gemma":[0.9964707,0.0019854968,0.00053048244,0.00044954405,0.00030227768,0.0002614232],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.001117945,0.00029035012,0.00057451753,0.0011633266,0.00037222423,0.0009618637,0.0006212729,0.00079047587,0.002822308],"category_scores_gemma":[0.0054479907,0.0004346177,0.00055752264,0.00068507233,0.00072368624,0.0010682853,0.00054965075,0.0012292091,0.0010252681],"study_design_candidate":"simulation_or_modeling","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0015442453,0.0002700096,0.22115283,0.00025695766,0.00035756337,0.00060137647,0.00032791638,0.09309081,0.5872645,0.021697827,0.0018562524,0.071579754],"study_design_scores_gemma":[0.000086741275,0.000315859,0.17856297,0.000013030967,0.00009951862,0.00061328284,0.000101485915,0.7492472,0.043229673,0.026274655,0.0013787171,0.00007691817],"about_ca_topic_score_codex":0.0021132685,"about_ca_topic_score_gemma":0.0023986618,"teacher_disagreement_score":0.002822308,"about_ca_system_score_codex":0.0006916816,"about_ca_system_score_gemma":0.00027266366,"threshold_uncertainty_score":0.009441555},"labels":[],"label_agreement":null},{"id":"W2946291524","doi":"10.1038/s41588-019-0438-3","title":"Author Correction: New genetic signals for lung function highlight pathways and chronic obstructive pulmonary disease associations across multiple ancestries","year":2019,"lang":"en","type":"erratum","venue":"Nature Genetics","topic":"Nutrition, Genetics, and Disease","field":"Biochemistry, Genetics and Molecular Biology","cited_by":9,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Institut universitaire de cardiologie et de pneumologie de Québec; Université Laval; St. Paul's Hospital; University of British Columbia","funders":"National Heart, Lung, and Blood Institute; Medical Research Council; National Institute for Health and Care Research; British Heart Foundation; Wellcome Trust","keywords":"Pulmonary disease; Biology; Lung function; Computational biology; Function (biology); Lung; Disease; Bioinformatics; Genetics; Internal medicine; Medicine","score_opus":0.010976727007390772,"score_gpt":0.26590533368335767,"score_spread":0.2549286066759669,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2946291524","genre_codex":"editorial","genre_gemma":"other","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"other","genre_consensus":null,"domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.00022934935,0.00058671413,0.0010329734,0.054863766,0.9385964,0.000022034938,0.0018067148,0.00044846963,0.0024136328],"genre_scores_gemma":[0.030775419,0.0061699557,0.012398201,0.1265895,0.4491591,0.00031603352,0.0068272976,0.004785374,0.3629792],"study_design_codex":"not_applicable","study_design_gemma":"not_applicable","domain_scores_codex":[0.9960508,0.0007274545,0.0006546803,0.00066559686,0.0014683475,0.0004331177],"domain_scores_gemma":[0.9730812,0.00805173,0.0012924866,0.001771644,0.014254172,0.0015487844],"candidate_categories":["research_integrity"],"consensus_categories":[],"category_scores_codex":[0.004286447,0.0022090804,0.0019021492,0.002965536,0.003085161,0.004017909,0.0040721367,0.0070922,0.08869456],"category_scores_gemma":[0.059272014,0.0012413291,0.0017318808,0.0017974055,0.0021267778,0.0019480917,0.0020476426,0.0112651605,0.03587266],"study_design_candidate":"not_applicable","study_design_consensus":"not_applicable","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.000041196694,0.000004675778,0.0001419539,0.00009526845,0.000020836194,0.0005319486,0.000027226444,0.000044865064,0.000056986057,0.0006745576,0.9948295,0.003530966],"study_design_scores_gemma":[0.00017053503,0.000025596863,0.0016994474,0.0005381806,0.000113858856,0.002893294,0.00013505196,0.0004715058,0.00068834703,0.0034826312,0.9897091,0.000072475246],"about_ca_topic_score_codex":0.015995571,"about_ca_topic_score_gemma":0.023659568,"teacher_disagreement_score":0.9929078,"about_ca_system_score_codex":0.0030595195,"about_ca_system_score_gemma":0.0048802737,"threshold_uncertainty_score":0.29671288},"labels":[],"label_agreement":null},{"id":"W2947236019","doi":"10.1038/s41588-018-0321-7","title":"New genetic signals for lung function highlight pathways and chronic obstructive pulmonary disease associations across multiple ancestries","year":2019,"lang":"en","type":"review","venue":"Nature Genetics","topic":"Chronic Obstructive Pulmonary Disease (COPD) Research","field":"Medicine","cited_by":599,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Institut universitaire de cardiologie et de pneumologie de Québec; Université Laval; St. Paul's Hospital; University of British Columbia","funders":"NIHR Nottingham Biomedical Research Centre; NIHR Leicester Biomedical Research Centre; Economic and Social Research Council; Biotechnology and Biological Sciences Research Council; Medical Research Council; University of Leicester; National Institutes of Health; Uppsala Universitet; National Heart, Lung, and Blood Institute; British Lung Foundation; Vetenskapsrådet; Hjärt-Lungfonden; National Institute for Health and Care Research; Bundesministerium für Bildung und Forschung; Deutsche Forschungsgemeinschaft; British Heart Foundation; Wellcome Trust","keywords":"Phenome; COPD; Genome-wide association study; Biology; Lung function; Generalizability theory; Genetic association; Pulmonary disease; Disease; Lung; Bioinformatics; Phenotype; Medicine; Genetics; Internal medicine; Gene; Single-nucleotide polymorphism; Genotype","score_opus":0.036754548698448186,"score_gpt":0.3454479003180905,"score_spread":0.3086933516196423,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2947236019","genre_codex":"review","genre_gemma":"review","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"review","genre_consensus":"review","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.00017838548,0.9981797,0.00018603311,0.0008293259,0.00019476908,0.0000015730051,0.00003505293,0.000006094395,0.00038910945],"genre_scores_gemma":[0.0012810341,0.99706656,0.00028549094,0.0005674299,0.0004139508,0.0000042500396,0.00005296233,0.000001692262,0.00032663843],"study_design_codex":"design_other","study_design_gemma":"observational","domain_scores_codex":[0.9998134,0.000046880417,0.000027446842,0.000052672483,0.000042853393,0.000016825586],"domain_scores_gemma":[0.9990619,0.00071394444,0.000072071525,0.00001968701,0.00009660446,0.000035875302],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0008973466,0.0007098534,0.0013639845,0.0013999075,0.00015641653,0.0008711693,0.00067715615,0.0011179385,0.0029450885],"category_scores_gemma":[0.0014181716,0.00019643609,0.00060927507,0.0015288689,0.0005420357,0.00086844095,0.00076738413,0.0017023684,0.0007262546],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00019496583,0.000034341778,0.0018251797,0.013959776,0.0005183019,0.00042235854,0.00009555044,0.00039425987,0.0016937027,0.009196966,0.024679337,0.9469853],"study_design_scores_gemma":[0.000078287325,0.00012630566,0.01009693,0.010875584,0.0012952337,0.0021206904,0.00021299685,0.00023630199,0.0005391969,0.017376183,0.9569799,0.00006239586],"about_ca_topic_score_codex":0.0014877624,"about_ca_topic_score_gemma":0.002439718,"teacher_disagreement_score":0.0029450885,"about_ca_system_score_codex":0.0005433223,"about_ca_system_score_gemma":0.0010057584,"threshold_uncertainty_score":0.00985235},"labels":[],"label_agreement":null},{"id":"W2947278243","doi":"10.1038/s41588-019-0407-x","title":"A catalog of genetic loci associated with kidney function from analyses of a million individuals","year":2019,"lang":"en","type":"review","venue":"Nature Genetics","topic":"Genetic Associations and Epidemiology","field":"Biochemistry, Genetics and Molecular Biology","cited_by":921,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Medpharmgene (Canada)","funders":"Eunice Kennedy Shriver National Institute of Child Health and Human Development; National Heart, Lung, and Blood Institute; National Institutes of Health; Novo Nordisk Fonden; Eisai; Wellcome Trust; Sirtex Medical; Albert-Ludwigs-Universität Freiburg; British Heart Foundation; Novo Nordisk; National Institute on Aging; CSL Behring; National Institute for Health and Care Research; Agence Nationale de la Recherche; Steno Diabetes Center Copenhagen; Eli Lilly and Company; AstraZeneca; Nestec; Yale University; American Regent; National Institute of Diabetes and Digestive and Kidney Diseases; Sanofi; Medical Research Council; Pfizer; Biogen; GlaxoSmithKline; University of Warwick","keywords":"Biology; Genetics; Evolutionary biology; Function (biology); Computational biology","score_opus":0.035936091062243894,"score_gpt":0.33414874190021143,"score_spread":0.29821265083796755,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2947278243","genre_codex":"review","genre_gemma":"review","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"review","genre_consensus":"review","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.00027153897,0.9958335,0.0010278369,0.001104425,0.00034702968,0.000009330196,0.0002644925,0.000029644178,0.0011121657],"genre_scores_gemma":[0.0008226103,0.9954047,0.001334397,0.00090721773,0.00052078173,0.000015194752,0.00033936833,0.0000056901263,0.000650087],"study_design_codex":"design_other","study_design_gemma":"observational","domain_scores_codex":[0.9995478,0.00008623429,0.000064897686,0.00011286441,0.00015897302,0.0000291892],"domain_scores_gemma":[0.9980708,0.0012211363,0.00015540529,0.00007251146,0.00037389368,0.00010625237],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0018585809,0.0013644997,0.0019073979,0.004162155,0.00022284471,0.0011045334,0.0012070287,0.0015144857,0.0026614985],"category_scores_gemma":[0.0029305248,0.00040527215,0.0006777049,0.0036135504,0.00065724633,0.0009789403,0.0010526598,0.0016713302,0.0014553476],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00008477149,0.000031265405,0.0015420356,0.005382123,0.00031174402,0.00025284593,0.00003431954,0.0002278533,0.0012624575,0.0030445748,0.045236066,0.9425899],"study_design_scores_gemma":[0.00008000901,0.00010461338,0.01311693,0.009020057,0.001106969,0.0035168093,0.000098585515,0.00020956456,0.00087248726,0.008359232,0.9634259,0.00008889013],"about_ca_topic_score_codex":0.0034698297,"about_ca_topic_score_gemma":0.004783494,"teacher_disagreement_score":0.004162155,"about_ca_system_score_codex":0.0007289932,"about_ca_system_score_gemma":0.0018574453,"threshold_uncertainty_score":0.009829223},"labels":[],"label_agreement":null},{"id":"W2948277145","doi":"10.1038/s41588-019-0449-0","title":"Publisher Correction: Multiancestry genome-wide association study of 520,000 subjects identifies 32 loci associated with stroke and stroke subtypes","year":2019,"lang":"en","type":"erratum","venue":"Nature Genetics","topic":"Genetic Associations and Epidemiology","field":"Biochemistry, Genetics and Molecular Biology","cited_by":32,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"McGill University; University of British Columbia; McMaster University; Population Health Research Institute","funders":"National Institute of Neurological Disorders and Stroke; National Institute of Diabetes and Digestive and Kidney Diseases; Agence Nationale de la Recherche; British Heart Foundation; Wellcome Trust","keywords":"Biology; Genome-wide association study; Stroke (engine); Genetics; Computational biology; Association (psychology); Genetic association; Genome; Bioinformatics; Gene; Single-nucleotide polymorphism; Psychology; Genotype; Engineering","score_opus":0.007306321768376621,"score_gpt":0.24038124609952838,"score_spread":0.23307492433115176,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2948277145","genre_codex":"editorial","genre_gemma":"other","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"other","genre_consensus":null,"domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.0001794229,0.00058187824,0.00096349197,0.01996814,0.9712115,0.00003243937,0.0036182245,0.00060276204,0.0028422312],"genre_scores_gemma":[0.022208571,0.004543278,0.014803536,0.06634547,0.32189447,0.0005974573,0.016215779,0.005981779,0.5474097],"study_design_codex":"not_applicable","study_design_gemma":"observational","domain_scores_codex":[0.99428684,0.0010568155,0.0012316831,0.00087877427,0.00207999,0.0004660588],"domain_scores_gemma":[0.9456818,0.01131105,0.002018042,0.00561706,0.03370879,0.0016631661],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0056573646,0.0029688003,0.0032143856,0.0068518557,0.0036010786,0.004993854,0.0062054754,0.005992471,0.14047013],"category_scores_gemma":[0.08565038,0.0021705467,0.0025908095,0.0047479006,0.0017510118,0.0026019253,0.0022439768,0.010442494,0.056326408],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.000033582364,0.0000054277502,0.00011512238,0.0001057749,0.000021793627,0.00018140592,0.000014485434,0.000044699365,0.00001876497,0.00034836048,0.9956982,0.0034123154],"study_design_scores_gemma":[0.00018521672,0.000028784118,0.0027575204,0.0006871442,0.00016807175,0.0010444621,0.00009736751,0.00069919525,0.00043073297,0.002565477,0.99125683,0.00007914323],"about_ca_topic_score_codex":0.036649402,"about_ca_topic_score_gemma":0.04894557,"teacher_disagreement_score":0.14047013,"about_ca_system_score_codex":0.0042679245,"about_ca_system_score_gemma":0.0056772837,"threshold_uncertainty_score":0.46991938},"labels":[],"label_agreement":null},{"id":"W2950103694","doi":"10.1038/s41588-018-0327-1","title":"Identification of new therapeutic targets for osteoarthritis through genome-wide analyses of UK Biobank data","year":2019,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Osteoarthritis Treatment and Mechanisms","field":"Medicine","cited_by":534,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"McGill University","funders":"Economic and Social Research Council; Medical Research Council; Versus Arthritis; National Institute for Health and Care Research; Understanding Society; NIHR Cambridge Biomedical Research Centre; Wellcome Trust; University of Essex","keywords":"Osteoarthritis; Biology; Genome-wide association study; Expression quantitative trait loci; Bioinformatics; Genetics; Gene; Medicine; Single-nucleotide polymorphism; Pathology; Genotype","score_opus":0.04619998071107864,"score_gpt":0.3448657757389106,"score_spread":0.29866579502783197,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2950103694","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.81283945,0.020584142,0.007038813,0.006156168,0.00016150354,0.00020739759,0.14775701,0.00012388434,0.0051316298],"genre_scores_gemma":[0.8949712,0.0065811407,0.008378459,0.0010917879,0.000112080044,0.0002751814,0.08737699,0.00007836433,0.0011347233],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9967416,0.0012663134,0.000610269,0.0006151197,0.0005132109,0.00025355097],"domain_scores_gemma":[0.9887573,0.005848181,0.003160074,0.00091270177,0.00091393606,0.0004078217],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0042246953,0.0004108828,0.0012256106,0.0040931883,0.00042100562,0.0013888109,0.00048814344,0.000664892,0.0049042143],"category_scores_gemma":[0.015756281,0.0003187371,0.0009769994,0.008815345,0.0003892495,0.000713812,0.0013192282,0.00078299956,0.000837643],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0046396004,0.00019309187,0.8264667,0.003609842,0.0045301295,0.0013586851,0.0015701724,0.0023674823,0.021433504,0.0022713572,0.036817834,0.09474153],"study_design_scores_gemma":[0.00030172803,0.00019399822,0.9570531,0.00060297776,0.0021614768,0.00078884995,0.00066206756,0.0012862231,0.001896678,0.0012220859,0.033768117,0.0000626236],"about_ca_topic_score_codex":0.019741345,"about_ca_topic_score_gemma":0.036603823,"teacher_disagreement_score":0.019741345,"about_ca_system_score_codex":0.0007021202,"about_ca_system_score_gemma":0.001760743,"threshold_uncertainty_score":0.039252877},"labels":[],"label_agreement":null},{"id":"W2950375827","doi":"10.1038/s41588-019-0397-8","title":"Genome-wide association study identifies 30 loci associated with bipolar disorder","year":2019,"lang":"en","type":"review","venue":"Nature Genetics","topic":"Genetic Associations and Epidemiology","field":"Biochemistry, Genetics and Molecular Biology","cited_by":1627,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"McGill University; Public Health Ontario; Montreal Neurological Institute and Hospital; Dalhousie University; University of Toronto; Centre for Addiction and Mental Health; Princess Margaret Cancer Centre; McGill University Health Centre","funders":"National Health and Medical Research Council; Center for Individualized Medicine, Mayo Clinic; H. Lundbeck A/S; Medical Research Council; Vetenskapsrådet; NSW Ministry of Health; Rheinische Friedrich-Wilhelms-Universität Bonn; National Institute of Mental Health; Aarhus Universitet; Stockholms Läns Landsting; Eli Lilly and Company; Lundbeckfonden; Schweizerischer Nationalfonds zur Förderung der Wissenschaftlichen Forschung; World Health Organization; Wellcome Trust; Agence Nationale de la Recherche; Generalitat de Catalunya; National Institute for Health and Care Research; European Regional Development Fund; Centro de Investigación Biomédica en Red de Salud Mental; Deutsche Forschungsgemeinschaft; Pfizer; Canadian Institutes of Health Research; National Science Foundation","keywords":"Biology; Genome-wide association study; Genetics; Bipolar disorder; Genetic association; Association (psychology); Genome; Computational biology; Evolutionary biology; Single-nucleotide polymorphism; Gene; Genotype; Neuroscience","score_opus":0.015386483854040449,"score_gpt":0.298881698793018,"score_spread":0.28349521493897756,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2950375827","genre_codex":"review","genre_gemma":"review","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"review","genre_consensus":"review","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.00018528676,0.99776244,0.0002240386,0.0005593889,0.00020262778,0.0000035428195,0.00007236742,0.000014291105,0.00097594527],"genre_scores_gemma":[0.0013637745,0.9969891,0.00038591374,0.00032688133,0.00019558425,0.000006709844,0.00012943489,0.0000025377624,0.00060018967],"study_design_codex":"design_other","study_design_gemma":"meta_analysis","domain_scores_codex":[0.999819,0.000039124352,0.000030132442,0.00004608393,0.00004720567,0.000018478462],"domain_scores_gemma":[0.9994717,0.00029436254,0.00006855883,0.000017010494,0.00010055233,0.000047898855],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00094265013,0.0009215693,0.0012889017,0.0023111668,0.00016996622,0.00089972373,0.0007449122,0.0011597008,0.0032221505],"category_scores_gemma":[0.00086766836,0.00024390702,0.00057499576,0.002877999,0.00044419826,0.0006298042,0.0007132673,0.0012645664,0.002390663],"study_design_candidate":"meta_analysis","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00012307854,0.000024669547,0.0007584916,0.0067254347,0.0002735655,0.00029314245,0.000023538902,0.00015062792,0.00075947127,0.0019977388,0.023902258,0.96496814],"study_design_scores_gemma":[0.00007426453,0.000116174306,0.009302937,0.0068566445,0.0008298507,0.0038269672,0.000063547326,0.00013801252,0.00061134814,0.0038928129,0.97423685,0.0000506628],"about_ca_topic_score_codex":0.0015097894,"about_ca_topic_score_gemma":0.003002394,"teacher_disagreement_score":0.0032221505,"about_ca_system_score_codex":0.00069066684,"about_ca_system_score_gemma":0.000991342,"threshold_uncertainty_score":0.010779142},"labels":[],"label_agreement":null},{"id":"W2950629294","doi":"10.1038/s41588-018-0122-z","title":"Multiplex assessment of protein variant abundance by massively parallel sequencing","year":2018,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Genomics and Phylogenetic Studies","field":"Biochemistry, Genetics and Molecular Biology","cited_by":522,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Canadian Institute for Advanced Research","funders":"National Institute of General Medical Sciences; National Cancer Institute; National Human Genome Research Institute; American Association for Cancer Research","keywords":"Biology; Multiplex; Massive parallel sequencing; Computational biology; Massively parallel; Genetics; DNA sequencing; Gene; Computer science; Parallel computing","score_opus":0.010216279106579068,"score_gpt":0.27224172650456085,"score_spread":0.2620254473979818,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2950629294","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.6845385,0.0021836865,0.3007873,0.0004606214,0.0002880371,0.00025110968,0.0058756904,0.0025049439,0.0031100872],"genre_scores_gemma":[0.7778936,0.0010154244,0.2131941,0.00039269173,0.00014646472,0.0003407401,0.0033414275,0.00028614252,0.0033894735],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9987178,0.0001617243,0.000068997426,0.0005037183,0.0004454579,0.000102251266],"domain_scores_gemma":[0.99881786,0.00035131568,0.0002428888,0.00022286114,0.00021651879,0.00014859605],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0014783011,0.00061385497,0.00058736326,0.0013756282,0.0005366924,0.0013075523,0.0005739866,0.00072652596,0.0010488229],"category_scores_gemma":[0.0022729782,0.00039301318,0.00037353774,0.0010687434,0.0005491773,0.0006236272,0.000839328,0.0010686752,0.00057503197],"study_design_candidate":"bench_or_experimental","study_design_consensus":"bench_or_experimental","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00036170636,0.00007033791,0.011506894,0.000098867284,0.0001483237,0.00008734548,0.00008668294,0.0007595422,0.96084267,0.0008113575,0.0007155181,0.024510743],"study_design_scores_gemma":[0.0000663347,0.0004967806,0.10896712,0.000045487115,0.0003074543,0.0014559231,0.00015345273,0.06561354,0.80613136,0.006898922,0.009758702,0.00010493538],"about_ca_topic_score_codex":0.0006783498,"about_ca_topic_score_gemma":0.0017476943,"teacher_disagreement_score":0.0014783011,"about_ca_system_score_codex":0.00036109675,"about_ca_system_score_gemma":0.00029678416,"threshold_uncertainty_score":0.007818103},"labels":[],"label_agreement":null},{"id":"W2952089656","doi":"10.1038/s41588-019-0463-2","title":"Publisher Correction: Exome sequencing highlights the role of wild-relative introgression in shaping the adaptive landscape of the wheat genome","year":2019,"lang":"en","type":"erratum","venue":"Nature Genetics","topic":"Genomics and Phylogenetic Studies","field":"Biochemistry, Genetics and Molecular Biology","cited_by":10,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Millar College of the Bible; University of Saskatchewan","funders":"","keywords":"Biology; Introgression; Exome sequencing; Genome; Exome; Genetics; DNA sequencing; Computational biology; Evolutionary biology; Gene; Mutation","score_opus":0.00880492142055727,"score_gpt":0.22025627341948498,"score_spread":0.2114513519989277,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2952089656","genre_codex":"editorial","genre_gemma":"other","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"other","genre_consensus":null,"domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.00014269218,0.000493357,0.00052275934,0.037905235,0.95712817,0.000012895843,0.0008064274,0.0002981284,0.0026903236],"genre_scores_gemma":[0.018087646,0.0061252667,0.0073905434,0.11462087,0.44211417,0.00018480263,0.0031540308,0.0026557422,0.40566692],"study_design_codex":"not_applicable","study_design_gemma":"not_applicable","domain_scores_codex":[0.9973398,0.00035226787,0.00049385196,0.00041600506,0.0011579706,0.00024005382],"domain_scores_gemma":[0.9756482,0.006108542,0.0011848107,0.0017858878,0.014019251,0.0012533484],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0029000263,0.0017149666,0.0016176961,0.003364765,0.003253257,0.004377972,0.0034490135,0.0065987334,0.053486038],"category_scores_gemma":[0.043208413,0.001108349,0.0013096313,0.0019487416,0.0024328968,0.002281371,0.0016393969,0.013290956,0.029752893],"study_design_candidate":"not_applicable","study_design_consensus":"not_applicable","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.000023650013,0.000005131172,0.000074475196,0.00007437099,0.000010696833,0.00039009037,0.000020695772,0.000042304535,0.00006714087,0.0006038854,0.993708,0.004979411],"study_design_scores_gemma":[0.000035986417,0.000014614716,0.0010237902,0.00024959235,0.00003932382,0.00086369214,0.00006722487,0.00022172606,0.00046018927,0.001715487,0.9952691,0.000039262213],"about_ca_topic_score_codex":0.01955724,"about_ca_topic_score_gemma":0.027523668,"teacher_disagreement_score":0.053486038,"about_ca_system_score_codex":0.0034027777,"about_ca_system_score_gemma":0.004191013,"threshold_uncertainty_score":0.17892861},"labels":[],"label_agreement":null},{"id":"W2952922105","doi":"10.1038/s41588-018-0105-0","title":"Discordant inheritance of chromosomal and extrachromosomal DNA elements contributes to dynamic disease evolution in glioblastoma","year":2018,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Cancer Genomics and Diagnostics","field":"Biochemistry, Genetics and Molecular Biology","cited_by":326,"is_retracted":false,"has_abstract":false,"route_ca_aff":false,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"","funders":"Génome Québec; Korea Health Industry Development Institute; Genome Canada; National Cancer Institute; National Institutes of Health; Cancer Prevention and Research Institute of Texas","keywords":"Extrachromosomal DNA; Biology; Genetics; Neurosphere; DNA; Genome; Cancer research; Gene; Cellular differentiation","score_opus":0.0028193169472135694,"score_gpt":0.24419465663022152,"score_spread":0.24137533968300795,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2952922105","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9985709,0.00032618144,0.000460081,0.00004545787,0.000004134514,0.0000029353262,0.00008816517,0.000013403467,0.000488693],"genre_scores_gemma":[0.998835,0.00019718661,0.00029514226,0.000033059485,0.0000047665694,0.000002761469,0.00012394549,0.000019694613,0.0004883835],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.999813,0.000019644007,0.000018230463,0.000048880764,0.000054451702,0.000045786117],"domain_scores_gemma":[0.99970716,0.00007238363,0.00010015793,0.00003425146,0.000039199447,0.00004690602],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00019191067,0.00013026042,0.00021675332,0.0009955785,0.00023105483,0.0005772323,0.00028276534,0.0003506204,0.0010087057],"category_scores_gemma":[0.00062433846,0.00017777598,0.0001562497,0.0005513569,0.0003109874,0.00026045673,0.00046435397,0.00041253178,0.0002379037],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00047340183,0.00005369589,0.119287595,0.000049118076,0.000081164944,0.0010893907,0.00033408173,0.0008328373,0.85494435,0.0013783765,0.00017412806,0.021301987],"study_design_scores_gemma":[0.000030082318,0.00023140188,0.8841789,0.000034881996,0.00015950149,0.005247706,0.0006141378,0.004450331,0.09917076,0.0023910478,0.0034523413,0.00003894096],"about_ca_topic_score_codex":0.0011114945,"about_ca_topic_score_gemma":0.002338481,"teacher_disagreement_score":0.0011114945,"about_ca_system_score_codex":0.00027476624,"about_ca_system_score_gemma":0.00019919244,"threshold_uncertainty_score":0.003374517},"labels":[],"label_agreement":null},{"id":"W2952949211","doi":"10.1038/ng.3980","title":"Ancient hybridization and strong adaptation to viruses across African vervet monkey populations","year":2017,"lang":"en","type":"article","venue":"Nature Genetics","topic":"HIV Research and Treatment","field":"Immunology and Microbiology","cited_by":137,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"McGill University","funders":"National Center for Research Resources; National Institute of Neurological Disorders and Stroke; National Institute of Allergy and Infectious Diseases; National Institutes of Health","keywords":"Biology; Vervet monkey; Evolutionary biology; Simian immunodeficiency virus; Genome; Adaptation (eye); Simian; Taxon; Reticulate; Natural selection; Phenotype; Genetics; Selection (genetic algorithm); Gene; Virus; Ecology","score_opus":0.051821933134744334,"score_gpt":0.3566667219332645,"score_spread":0.30484478879852017,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2952949211","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99743026,0.0004107846,0.00039281143,0.00011339838,0.000010465809,0.0000050607177,0.000020837719,0.0000073769784,0.0016090284],"genre_scores_gemma":[0.9987041,0.00028172595,0.00027190597,0.00008446517,0.000014297337,0.000006220008,0.000033570028,0.000008658501,0.0005950836],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.99932265,0.00024408415,0.000027897078,0.00018349913,0.00008289329,0.00013894304],"domain_scores_gemma":[0.9995665,0.00012926433,0.000096413976,0.00008823489,0.000057405898,0.00006220201],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0008354743,0.00024469336,0.00034945292,0.0009024324,0.001551186,0.0012812988,0.00043823122,0.0008829795,0.0030467035],"category_scores_gemma":[0.001496441,0.00025241022,0.00020085798,0.00077114475,0.0015492796,0.0007071492,0.0013894129,0.0010229738,0.00029139867],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0022552684,0.00020950881,0.21206045,0.000220588,0.0003391178,0.0028485523,0.014067186,0.0004609394,0.68311924,0.008252986,0.0002955715,0.07587064],"study_design_scores_gemma":[0.00006108579,0.00069788145,0.9447396,0.00017400394,0.00018367337,0.008003251,0.008275524,0.0012814478,0.020103686,0.0056369384,0.01078592,0.000056972873],"about_ca_topic_score_codex":0.0018250725,"about_ca_topic_score_gemma":0.0035964039,"teacher_disagreement_score":0.0030467035,"about_ca_system_score_codex":0.0006321574,"about_ca_system_score_gemma":0.0002784156,"threshold_uncertainty_score":0.010192215},"labels":[],"label_agreement":null},{"id":"W2954569314","doi":"10.1038/s41588-019-0461-4","title":"Mutagenesis-based protein structure determination","year":2019,"lang":"en","type":"article","venue":"Nature Genetics","topic":"RNA and protein synthesis mechanisms","field":"Biochemistry, Genetics and Molecular Biology","cited_by":5,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Ontario Stroke Network","funders":"National Institute of General Medical Sciences; National Human Genome Research Institute","keywords":"Biology; Mutagenesis; Computational biology; Genetics; Sequence (biology); Protein structure; Basis (linear algebra); Mutation; Evolutionary biology; Gene; Biochemistry","score_opus":0.004317930327268983,"score_gpt":0.2334147559995398,"score_spread":0.22909682567227083,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2954569314","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.6704332,0.0011888637,0.31583452,0.00057008717,0.00023280414,0.0004963207,0.002108642,0.0020520848,0.007083414],"genre_scores_gemma":[0.827857,0.0010173665,0.1612709,0.00025621132,0.000019388144,0.00021566042,0.0035201688,0.000561672,0.0052815853],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9994893,0.00016692048,0.000044533208,0.00010318233,0.00014027189,0.00005579008],"domain_scores_gemma":[0.99943227,0.00017866862,0.00006871689,0.00012404763,0.00014044551,0.000055835964],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0007760859,0.0007152369,0.0005568115,0.0005582152,0.0006878872,0.0005311724,0.00083832163,0.00060325646,0.0018906296],"category_scores_gemma":[0.0009223603,0.00047431866,0.00042461578,0.00040699576,0.00037954663,0.00027522794,0.0004086247,0.0017330775,0.00096242526],"study_design_candidate":"bench_or_experimental","study_design_consensus":"bench_or_experimental","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00005646657,0.000031069336,0.00017920174,0.000029713143,0.000013641109,0.000047633264,0.000021794793,0.0004979274,0.994292,0.000556523,0.00020241059,0.004071701],"study_design_scores_gemma":[0.000010372265,0.000047141715,0.0006274497,0.0000037633054,0.000014082595,0.00014988836,0.000011062382,0.0053154007,0.99068296,0.00014224341,0.0029865832,0.000009131642],"about_ca_topic_score_codex":0.001744599,"about_ca_topic_score_gemma":0.0042814086,"teacher_disagreement_score":0.0018906296,"about_ca_system_score_codex":0.00065747317,"about_ca_system_score_gemma":0.0006371985,"threshold_uncertainty_score":0.006324768},"labels":[],"label_agreement":null},{"id":"W2955994579","doi":"10.1038/s41588-019-0494-8","title":"A compendium of promoter-centered long-range chromatin interactions in the human genome","year":2019,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Genomics and Chromatin Dynamics","field":"Biochemistry, Genetics and Molecular Biology","cited_by":409,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"SickKids Foundation; Hospital for Sick Children; University Health Network","funders":"National Institute of Environmental Health Sciences; National Human Genome Research Institute; Ludwig Institute for Cancer Research; Ministry of Health and Welfare; Ministry of Science, ICT and Future Planning; Korea Advanced Institute of Science and Technology; National Institutes of Health; U.S. Department of Health and Human Services","keywords":"Biology; Chromatin; Enhancer; Interactome; Genetics; Gene; Promoter; ChIA-PET; Regulatory sequence; Computational biology; Genome; Human genome; Chromosome conformation capture; Regulation of gene expression; Transcription factor; Chromatin remodeling; Gene expression","score_opus":0.007946150960639395,"score_gpt":0.2617073225402374,"score_spread":0.253761171579598,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2955994579","genre_codex":"methods","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":null,"domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.044556033,0.25451124,0.5439432,0.008894345,0.006769346,0.00033667,0.08430748,0.01419945,0.042482145],"genre_scores_gemma":[0.119723804,0.19858052,0.532226,0.005153018,0.0041855206,0.00058599986,0.10896289,0.004671161,0.025911056],"study_design_codex":"design_other","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9995141,0.000060461338,0.0000854087,0.00015411525,0.00015717064,0.00002878276],"domain_scores_gemma":[0.9971565,0.0013995725,0.00019129876,0.0007023405,0.00041007713,0.0001402308],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0010562988,0.0011199504,0.0013967601,0.003023126,0.0007087607,0.002122032,0.001197437,0.0006583058,0.0046000537],"category_scores_gemma":[0.0031151667,0.0010630484,0.0008094392,0.0030007074,0.0005777866,0.001655505,0.0011679911,0.0022200656,0.0025127144],"study_design_candidate":"bench_or_experimental","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00030016564,0.00005747666,0.002577524,0.0044010193,0.00032045375,0.00066975754,0.0005411637,0.007891488,0.08980183,0.016172552,0.088156,0.7891106],"study_design_scores_gemma":[0.000025766234,0.00010667693,0.011887192,0.00084537704,0.0004892475,0.0018939096,0.00008851161,0.0070249904,0.025712201,0.020315968,0.931474,0.0001361715],"about_ca_topic_score_codex":0.0019474956,"about_ca_topic_score_gemma":0.006275187,"teacher_disagreement_score":0.0046000537,"about_ca_system_score_codex":0.0004865598,"about_ca_system_score_gemma":0.0014844269,"threshold_uncertainty_score":0.015388668},"labels":[],"label_agreement":null},{"id":"W2960372990","doi":"10.1038/s41588-019-0439-2","title":"Genome-wide association study identifies eight risk loci and implicates metabo-psychiatric origins for anorexia nervosa","year":2019,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Eating Disorders and Behaviors","field":"Psychology","cited_by":1181,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University Health Network; Hospital for Sick Children; Centre for Addiction and Mental Health; University of Toronto","funders":"North Carolina Translational and Clinical Sciences Institute, University of North Carolina at Chapel Hill; National Human Genome Research Institute; National Institute of Mental Health; National Institute on Alcohol Abuse and Alcoholism; National Institutes of Health; National and Kapodistrian University of Athens; Eli Lilly and Company; Lundbeckfonden; Auckland District Health Board; Flinders University; Children's Hospital of Philadelphia; King's College London; Medical Research Council; Department of Health and Social Care; Curtin University of Technology; Louis and Harold Price Foundation; Academy for Eating Disorders; Wellcome Trust; Genesis Pharma; Shire; Maudsley Charity; Foundation of Hope for Research and Treatment of Mental Illness; H. Lundbeck A/S; Sunovion; National Institute for Health and Care Research; Sanofi; GlaxoSmithKline; Pfizer; National Health and Medical Research Council; AstraZeneca; NIHR BioResource; Western Sydney University; Bristol-Myers Squibb","keywords":"Biology; Anorexia nervosa; Genome-wide association study; Association (psychology); Genetic association; Genetics; Bioinformatics; Psychiatry; Eating disorders; Single-nucleotide polymorphism; Gene; Medicine; Genotype; Psychology","score_opus":0.008154788595431794,"score_gpt":0.29618794457217584,"score_spread":0.28803315597674406,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2960372990","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99086106,0.0023940743,0.0017928985,0.0011053093,0.00007659481,0.000032274,0.0009669006,0.000037741815,0.0027333354],"genre_scores_gemma":[0.99527836,0.0009152687,0.0019077857,0.00015290511,0.000031378924,0.000025247915,0.0006145344,0.000008260408,0.0010663951],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9997044,0.0001202816,0.000024622761,0.00006671149,0.00004730111,0.00003655746],"domain_scores_gemma":[0.9995345,0.00016798123,0.00013102892,0.000038552833,0.00004421984,0.00008373856],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00050777354,0.00048797342,0.00022536798,0.0010056323,0.0005314266,0.000641135,0.00034861258,0.0005842115,0.0040076906],"category_scores_gemma":[0.0013633606,0.00023549772,0.0005614857,0.0009314793,0.00035453335,0.00015412159,0.0005207579,0.00087032054,0.00023099734],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0007734077,0.00013064906,0.970633,0.00009705624,0.00089151936,0.0010712174,0.00021478333,0.0002655784,0.008199038,0.000690231,0.0011581623,0.015875556],"study_design_scores_gemma":[0.00005169338,0.00008256184,0.99459153,0.000059050562,0.00044385938,0.0011979695,0.00019940459,0.00058262196,0.00065313384,0.0006735735,0.0014536977,0.000010822613],"about_ca_topic_score_codex":0.006442429,"about_ca_topic_score_gemma":0.014883651,"teacher_disagreement_score":0.006442429,"about_ca_system_score_codex":0.00023211405,"about_ca_system_score_gemma":0.00037957338,"threshold_uncertainty_score":0.013407111},"labels":[],"label_agreement":null},{"id":"W2962165257","doi":"10.1038/s41588-019-0447-2","title":"Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity","year":2019,"lang":"en","type":"erratum","venue":"Nature Genetics","topic":"Genetic Associations and Epidemiology","field":"Biochemistry, Genetics and Molecular Biology","cited_by":9,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"York University; Université de Montréal; Dalhousie University; Montreal Heart Institute","funders":"Medical Research Council; European Hematology Association; National Institute for Health and Care Research; Steno Diabetes Center Aarhus; Wellcome Trust; British Heart Foundation; Lundbeckfonden; Cancer Research UK","keywords":"Energy expenditure; Biology; Body mass index; Obesity; Index (typography); Energy metabolism; Control (management); Genetics; Bioinformatics; Endocrinology; Computer science","score_opus":0.007475233384935678,"score_gpt":0.2193475451258657,"score_spread":0.21187231174093002,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2962165257","genre_codex":"editorial","genre_gemma":"other","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"other","genre_consensus":null,"domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.00015356175,0.0006314732,0.00058849057,0.033283256,0.96015066,0.000017308446,0.001034423,0.00024354983,0.0038973028],"genre_scores_gemma":[0.016906902,0.0069299745,0.0073300046,0.07822337,0.36713973,0.00021308188,0.004473057,0.0020942504,0.51668954],"study_design_codex":"not_applicable","study_design_gemma":"not_applicable","domain_scores_codex":[0.99705935,0.0004353252,0.0005560842,0.00043991578,0.0012610026,0.0002483289],"domain_scores_gemma":[0.9782823,0.0060922764,0.00093668565,0.0013931189,0.012311233,0.0009844468],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0032164399,0.0020519295,0.001589866,0.0034955814,0.0030427086,0.0033763284,0.0031285137,0.0052098967,0.064031],"category_scores_gemma":[0.040078606,0.0010000269,0.0015447617,0.0021457502,0.0016507503,0.0015879521,0.0014111385,0.010182515,0.03386013],"study_design_candidate":"not_applicable","study_design_consensus":"not_applicable","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.000028498414,0.000004468927,0.00007680664,0.00007402204,0.000010010289,0.0003227171,0.00001947046,0.00003176261,0.000047205707,0.00058188156,0.99400514,0.0047981935],"study_design_scores_gemma":[0.00004521529,0.000018023724,0.00086487434,0.0003114311,0.000047174424,0.00100388,0.000062907115,0.00020406724,0.00033511943,0.0016324508,0.99543935,0.00003560077],"about_ca_topic_score_codex":0.018408965,"about_ca_topic_score_gemma":0.029648613,"teacher_disagreement_score":0.064031,"about_ca_system_score_codex":0.0027758847,"about_ca_system_score_gemma":0.004022717,"threshold_uncertainty_score":0.21420503},"labels":[],"label_agreement":null},{"id":"W2968804311","doi":"10.1038/s41588-019-0495-7","title":"Author Correction: Genetic meta-analysis of diagnosed Alzheimer’s disease identifies new risk loci and implicates Aβ, tau, immunity and lipid processing","year":2019,"lang":"en","type":"erratum","venue":"Nature Genetics","topic":"Alzheimer's disease research and treatments","field":"Medicine","cited_by":91,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Occupational Cancer Research Centre; University of Toronto","funders":"National Institute on Aging; Avid Radiopharmaceuticals; Allergan; National Institutes of Health; Genentech; Grifols; H. Lundbeck A/S; Servier; Parkinson's UK; Eisai; Wellcome Trust; Agence Nationale de la Recherche; Rosetrees Trust; National Institute for Health and Care Research; Medical Research Council; Biogen; Amgen; Pfizer; Eli Lilly and Company; Otsuka Pharmaceutical","keywords":"Biology; Disease; Meta-analysis; Immunity; Computational biology; Genetics; Genealogy; Evolutionary biology; Internal medicine; Immune system; History","score_opus":0.04757681677266829,"score_gpt":0.35303439537469544,"score_spread":0.30545757860202716,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2968804311","genre_codex":"editorial","genre_gemma":"other","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"other","genre_consensus":null,"domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.00022047781,0.0014816734,0.0014207105,0.054398127,0.93289983,0.000057188656,0.0075449985,0.0006432718,0.0013337707],"genre_scores_gemma":[0.03965871,0.006881097,0.017913412,0.21023037,0.5124944,0.0014595059,0.014583183,0.006197938,0.19058141],"study_design_codex":"not_applicable","study_design_gemma":"not_applicable","domain_scores_codex":[0.9888094,0.0027800463,0.002403666,0.0020217118,0.003169343,0.00081580575],"domain_scores_gemma":[0.91751766,0.035729796,0.0054978332,0.0067356587,0.031804517,0.00271456],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.017649522,0.004340269,0.005075373,0.005316858,0.0029443158,0.0046441774,0.0061485525,0.0078007123,0.10523211],"category_scores_gemma":[0.1904799,0.0025680438,0.0051181633,0.0047859917,0.0021426731,0.0025814981,0.002567206,0.010668785,0.026650075],"study_design_candidate":"not_applicable","study_design_consensus":"not_applicable","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00010340309,0.0000039082724,0.0002817881,0.00041746936,0.00016985968,0.00024775867,0.000019799369,0.000048953745,0.000023279441,0.00026141462,0.99635065,0.002071702],"study_design_scores_gemma":[0.0028720354,0.00010668173,0.00659354,0.004355197,0.0039598946,0.003993949,0.00022699959,0.0024583172,0.00090534514,0.010942764,0.963305,0.00028023814],"about_ca_topic_score_codex":0.025385913,"about_ca_topic_score_gemma":0.039490253,"teacher_disagreement_score":0.10523211,"about_ca_system_score_codex":0.003950162,"about_ca_system_score_gemma":0.009154921,"threshold_uncertainty_score":0.35203654},"labels":[],"label_agreement":null},{"id":"W2970142068","doi":"10.1038/s41588-019-0487-7","title":"Ultrarare variants drive substantial cis heritability of human gene expression","year":2019,"lang":"en","type":"article","venue":"Nature Genetics","topic":"RNA Research and Splicing","field":"Biochemistry, Genetics and Molecular Biology","cited_by":129,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"McGill University; McGill University and Génome Québec Innovation Centre","funders":"National Institute of General Medical Sciences; National Heart, Lung, and Blood Institute; National Institutes of Health; National Human Genome Research Institute; U.S. Department of Health and Human Services","keywords":"Biology; Heritability; Genetics; Gene; Expression (computer science); Gene expression; Computational biology","score_opus":0.007655971146183628,"score_gpt":0.28018332269132595,"score_spread":0.27252735154514235,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2970142068","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.97266495,0.0006285415,0.02176776,0.00017285238,0.00012472288,0.000032247943,0.0014803952,0.0005565092,0.0025720212],"genre_scores_gemma":[0.99119765,0.00017136289,0.0045175133,0.00018827301,0.000063104766,0.000022470032,0.00072975684,0.00034879107,0.0027610636],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9994665,0.00008930632,0.00005438141,0.00019773116,0.0001240714,0.000068133886],"domain_scores_gemma":[0.99908566,0.00039199725,0.0001296366,0.00022540476,0.00005133771,0.0001160427],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00039153552,0.0004717557,0.0005921148,0.0005914188,0.00031072096,0.00041686313,0.00041697462,0.00057444826,0.0071114963],"category_scores_gemma":[0.00047372628,0.0004448116,0.0005097057,0.00034954387,0.00039458973,0.00020087505,0.0006072839,0.0010737834,0.0012148913],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00023977847,0.000056243418,0.0026616899,0.00003485542,0.000072734365,0.000841729,0.000068884925,0.00023815678,0.98877907,0.0015841628,0.00018846366,0.005234173],"study_design_scores_gemma":[0.000117176816,0.00065223913,0.120548174,0.00003648578,0.00034421004,0.01356424,0.00020087285,0.0041594524,0.8482197,0.0024319657,0.009637168,0.00008830844],"about_ca_topic_score_codex":0.0005351247,"about_ca_topic_score_gemma":0.0017032964,"teacher_disagreement_score":0.0071114963,"about_ca_system_score_codex":0.00015680403,"about_ca_system_score_gemma":0.00013581911,"threshold_uncertainty_score":0.0237903},"labels":[],"label_agreement":null},{"id":"W2970459958","doi":"10.1038/s41588-019-0484-x","title":"A method for genome-wide genealogy estimation for thousands of samples","year":2019,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Forensic and Genetic Research","field":"Biochemistry, Genetics and Molecular Biology","cited_by":597,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Université du Québec à Montréal","funders":"Engineering and Physical Sciences Research Council; Missouri Soybean Merchandising Council; Research Councils UK; Wellcome Trust; Wellcome","keywords":"Biology; Introgression; Selection (genetic algorithm); Evolutionary biology; Genome; 1000 Genomes Project; Natural selection; Haplotype; Population; Directional selection; Genetics; Human genome; Allele; Genetic variation; Genotype; Gene; Single-nucleotide polymorphism; Artificial intelligence; Demography; Computer science","score_opus":0.013809416662594902,"score_gpt":0.3403765262111521,"score_spread":0.3265671095485572,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2970459958","genre_codex":"methods","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":null,"domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.005950717,0.0002695927,0.9908556,0.00008323096,0.00005797008,0.00007713625,0.0007165866,0.0017078951,0.00028126664],"genre_scores_gemma":[0.04134828,0.00016981133,0.95420015,0.000081038605,0.00008410752,0.00034192795,0.0021789654,0.00020680753,0.001388989],"study_design_codex":"design_other","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9977527,0.0005781991,0.00016406382,0.0007595313,0.0006512766,0.00009425132],"domain_scores_gemma":[0.9922686,0.0045234757,0.00034324123,0.0018128739,0.00087320164,0.00017859298],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00368618,0.00090775895,0.0014963348,0.0030617686,0.0012142013,0.0015207226,0.0023231592,0.0014608379,0.0044290717],"category_scores_gemma":[0.018891469,0.00094511156,0.0012349143,0.003090704,0.0006417371,0.0015370959,0.002152109,0.0023176388,0.0027223015],"study_design_candidate":"bench_or_experimental","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00051203603,0.0001695218,0.017502716,0.000394753,0.0011037166,0.00037361207,0.00043108466,0.045319807,0.03122673,0.017612863,0.012682038,0.87267107],"study_design_scores_gemma":[0.00016896233,0.00012619406,0.014866269,0.00008523682,0.00035333945,0.0020502168,0.00013474101,0.86253595,0.020642255,0.07282505,0.026025048,0.00018672574],"about_ca_topic_score_codex":0.004463697,"about_ca_topic_score_gemma":0.0077881273,"teacher_disagreement_score":0.004463697,"about_ca_system_score_codex":0.0005200251,"about_ca_system_score_gemma":0.001637691,"threshold_uncertainty_score":0.019494593},"labels":[],"label_agreement":null},{"id":"W2971585857","doi":"10.1038/s41588-019-0480-1","title":"A reference genome for pea provides insight into legume genome evolution","year":2019,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Genetic and Environmental Crop Studies","field":"Agricultural and Biological Sciences","cited_by":557,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Saskatchewan","funders":"Agence Nationale de la Recherche","keywords":"Biology; Genome; Genetics; Genome evolution; Reference genome; Whole genome sequencing; Gene; Genomics; Evolutionary biology","score_opus":0.012052981978151783,"score_gpt":0.2071378060117453,"score_spread":0.19508482403359353,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2971585857","genre_codex":"methods","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":null,"domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.13497789,0.034532186,0.4504389,0.002800775,0.002938338,0.00050222455,0.31154197,0.019433511,0.04283421],"genre_scores_gemma":[0.096666,0.008434878,0.2546774,0.0005260674,0.0001901547,0.00025096134,0.62578946,0.0017461277,0.011718906],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9995339,0.00004803551,0.00004576792,0.0001756533,0.00013799762,0.000058712332],"domain_scores_gemma":[0.9991078,0.00009185375,0.00009113685,0.0001947673,0.00044516104,0.000069236194],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0008086652,0.0010985631,0.00092327775,0.0028594476,0.000921813,0.00090263714,0.0010761095,0.0012915812,0.006525346],"category_scores_gemma":[0.001957971,0.00044731563,0.00092177297,0.004012326,0.00020662275,0.000795152,0.00084007,0.0011399714,0.007057591],"study_design_candidate":"bench_or_experimental","study_design_consensus":"bench_or_experimental","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0010088875,0.000096450356,0.0045780265,0.0024369613,0.00029318527,0.0016123544,0.00042693308,0.002080174,0.70696217,0.00818061,0.04655573,0.22576857],"study_design_scores_gemma":[0.00009753632,0.0003409818,0.02988553,0.00050937675,0.00040973575,0.0023401063,0.00016192625,0.003358636,0.09983391,0.0063960976,0.85653645,0.00012974214],"about_ca_topic_score_codex":0.0041923844,"about_ca_topic_score_gemma":0.006881385,"teacher_disagreement_score":0.006525346,"about_ca_system_score_codex":0.00067775015,"about_ca_system_score_gemma":0.0012508776,"threshold_uncertainty_score":0.021829426},"labels":[],"label_agreement":null},{"id":"W2976552964","doi":"10.1038/s41588-019-0498-4","title":"Postzygotic inactivating mutations of RHOA cause a mosaic neuroectodermal syndrome","year":2019,"lang":"en","type":"article","venue":"Nature Genetics","topic":"RNA regulation and disease","field":"Biochemistry, Genetics and Molecular Biology","cited_by":45,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"McGill Genome Centre; Montreal Children's Hospital; McGill University; McGill University Health Centre","funders":"Eunice Kennedy Shriver National Institute of Child Health and Human Development; National Institute of Neurological Disorders and Stroke; Canadian Institutes of Health Research; Agence Nationale de la Recherche","keywords":"Biology; Hypopigmentation; RHOA; Genetics; Mutation; Gene","score_opus":0.005593748504071647,"score_gpt":0.2500484490332383,"score_spread":0.24445470052916665,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2976552964","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9946272,0.0003468702,0.0022334675,0.0001156771,0.0000308606,0.000019591345,0.00016404461,0.00009271473,0.0023696725],"genre_scores_gemma":[0.9964316,0.00020950104,0.0013620836,0.000030485347,0.000021142292,0.000010856851,0.00009058173,0.00003542147,0.0018083213],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9998274,0.000025689322,0.000022129596,0.00003405201,0.00006448662,0.000026169104],"domain_scores_gemma":[0.99963593,0.00010160829,0.00011301848,0.000030566647,0.000013453872,0.00010548767],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00011391309,0.0007473607,0.0002717688,0.00074497465,0.00033963835,0.0002603239,0.0003245791,0.0007645302,0.0018529642],"category_scores_gemma":[0.00042431612,0.00028975337,0.00024317374,0.00035783337,0.00062013796,0.00019255107,0.00052649115,0.0007522406,0.00056046096],"study_design_candidate":"bench_or_experimental","study_design_consensus":"bench_or_experimental","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0004993285,0.00008101535,0.0064764093,0.000046127978,0.000048934406,0.038232468,0.0001873718,0.00032954832,0.9456169,0.0024525034,0.00030979657,0.0057196096],"study_design_scores_gemma":[0.00026041444,0.0007589682,0.19180332,0.000028104196,0.0002736485,0.25239772,0.00042047302,0.004777982,0.53760844,0.0019648417,0.009648053,0.00005803017],"about_ca_topic_score_codex":0.00048858195,"about_ca_topic_score_gemma":0.0009987311,"teacher_disagreement_score":0.0018529642,"about_ca_system_score_codex":0.00017927993,"about_ca_system_score_gemma":0.0002873687,"threshold_uncertainty_score":0.006198764},"labels":[],"label_agreement":null},{"id":"W2977833465","doi":"10.1038/s41588-019-0504-x","title":"Target genes, variants, tissues and transcriptional pathways influencing human serum urate levels","year":2019,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Gout, Hyperuricemia, Uric Acid","field":"Medicine","cited_by":430,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Medpharmgene (Canada); Centre Hospitalier de l’Université de Montréal","funders":"National Institute of Diabetes and Digestive and Kidney Diseases; National Heart, Lung, and Blood Institute; National Institute of Arthritis and Musculoskeletal and Skin Diseases; Medical Research Council; British Heart Foundation; Albert-Ludwigs-Universität Freiburg; National Human Genome Research Institute; Wellcome Trust; Nederlandse Organisatie voor Wetenschappelijk Onderzoek; Agence Nationale de la Recherche; GlaxoSmithKline; Deutsche Forschungsgemeinschaft; Eunice Kennedy Shriver National Institute of Child Health and Human Development; European Regional Development Fund; European Commission; National Institute of General Medical Sciences; National Institute for Health and Care Research; American Heart Association; National Institutes of Health; U.S. Department of Health and Human Services","keywords":"Biology; Genome-wide association study; Expression quantitative trait loci; Genetics; Pleiotropy; Quantitative trait locus; Gene; Genetic association; Single-nucleotide polymorphism; Phenotype; Genotype","score_opus":0.017356402111621736,"score_gpt":0.2619559392345549,"score_spread":0.24459953712293317,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2977833465","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.98916,0.0032997222,0.0027837255,0.00020220854,0.0000378492,0.000013427212,0.002317738,0.0000878552,0.0020974772],"genre_scores_gemma":[0.9953501,0.00083119364,0.0010568339,0.000071982024,0.000022761493,0.000013292535,0.0010131324,0.000033133034,0.0016074983],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9998752,0.000027636712,0.000007923188,0.000039423645,0.00002497307,0.000024880195],"domain_scores_gemma":[0.9997961,0.00009089365,0.000045255423,0.000017411301,0.000015774956,0.0000346237],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00012878563,0.0002297988,0.0002702044,0.00039956468,0.00013637987,0.00044834038,0.00011626572,0.00021236065,0.0028822566],"category_scores_gemma":[0.0003130283,0.00012249725,0.00028992578,0.00041737664,0.00014076573,0.000077138895,0.000165758,0.00021434648,0.00036642342],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00277401,0.000048999053,0.098468795,0.00018503304,0.0003101378,0.0015316206,0.00019662995,0.00042221963,0.87931997,0.00080387713,0.0006966296,0.015242004],"study_design_scores_gemma":[0.0001214345,0.00035306526,0.84348035,0.000050196846,0.0006039143,0.004933151,0.00032258948,0.0024413485,0.14037631,0.00126135,0.006029565,0.000026738326],"about_ca_topic_score_codex":0.0013242218,"about_ca_topic_score_gemma":0.0011505592,"teacher_disagreement_score":0.0028822566,"about_ca_system_score_codex":0.00014072546,"about_ca_system_score_gemma":0.00013227726,"threshold_uncertainty_score":0.009642065},"labels":[],"label_agreement":null},{"id":"W2979722574","doi":"10.1038/s41588-019-0527-3","title":"Author Correction: Postzygotic inactivating mutations of RHOA cause a mosaic neuroectodermal syndrome","year":2019,"lang":"en","type":"erratum","venue":"Nature Genetics","topic":"Ubiquitin and proteasome pathways","field":"Biochemistry, Genetics and Molecular Biology","cited_by":2,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"McGill Genome Centre; McGill University; Montreal Children's Hospital; McGill University Health Centre","funders":"","keywords":"Biology; RHOA; Mosaic; Genetics; Mutation; Gene","score_opus":0.012622854899024717,"score_gpt":0.26969660682619306,"score_spread":0.25707375192716836,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2979722574","genre_codex":"editorial","genre_gemma":"other","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"other","genre_consensus":null,"domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.00033215553,0.00075071584,0.00067611126,0.028620165,0.96710825,0.000014454344,0.00044575962,0.00024084511,0.0018115527],"genre_scores_gemma":[0.043213192,0.010401772,0.00933774,0.08332507,0.54362047,0.00019805695,0.0025409986,0.002474663,0.304888],"study_design_codex":"not_applicable","study_design_gemma":"not_applicable","domain_scores_codex":[0.99778664,0.00026896544,0.0004022861,0.00035313927,0.00095134525,0.00023757856],"domain_scores_gemma":[0.9880189,0.0032965962,0.0007687447,0.00072269724,0.0062757744,0.00091732194],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0019774127,0.0021626235,0.0017630443,0.003046977,0.0025641578,0.0027292415,0.0035925747,0.008836394,0.03060991],"category_scores_gemma":[0.027749717,0.0011410437,0.0015498579,0.0012839094,0.0018350327,0.0015507414,0.0013285549,0.0096676685,0.016403994],"study_design_candidate":"not_applicable","study_design_consensus":"not_applicable","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00006348579,0.000012507807,0.00012854554,0.00013259074,0.00003274382,0.004259138,0.000037960865,0.00008627992,0.0001891033,0.00095805706,0.9878826,0.0062169433],"study_design_scores_gemma":[0.00010533226,0.000037438218,0.0010709983,0.00026302334,0.00010668086,0.008453538,0.000082728606,0.00048040118,0.0011507599,0.0016720137,0.9865108,0.0000663877],"about_ca_topic_score_codex":0.009388239,"about_ca_topic_score_gemma":0.01208097,"teacher_disagreement_score":0.03060991,"about_ca_system_score_codex":0.0027259756,"about_ca_system_score_gemma":0.0025985613,"threshold_uncertainty_score":0.10240036},"labels":[],"label_agreement":null},{"id":"W2980879969","doi":"10.1038/s41588-019-0511-y","title":"Genetic architecture of subcortical brain structures in 38,851 individuals","year":2019,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Genetic Associations and Epidemiology","field":"Biochemistry, Genetics and Molecular Biology","cited_by":288,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Holland Bloorview Kids Rehabilitation Hospital; McGill University; University of Calgary; Douglas Mental Health University Institute; University of Toronto; SickKids Foundation; Hospital for Sick Children","funders":"Medical Research Foundation; National Institute of Neurological Disorders and Stroke; National Institute of Mental Health; National Heart, Lung, and Blood Institute; National Medical Research Council; National Center for Advancing Translational Sciences; Medical Research Council; National Health and Medical Research Council; Norges Forskningsråd; Canadian HIV Trials Network, Canadian Institutes of Health Research; Nederlandse Organisatie voor Wetenschappelijk Onderzoek; National Center for Research Resources; Agence Nationale de la Recherche; Deutsche Forschungsgemeinschaft; Instituto de Salud Carlos III; Mrs Gladys Row Fogo Charitable Trust; Fonds De La Recherche Scientifique - FNRS; Ministerio de Economía y Competitividad; Department of Biotechnology, Ministry of Science and Technology, India; Research Councils UK; South African Medical Research Council; National Institute on Aging; Alzheimer's Association; Biotechnology and Biological Sciences Research Council; Michael J. Fox Foundation for Parkinson's Research; Lundbeckfonden; National Institute of General Medical Sciences; Burroughs Wellcome Fund; U.S. Department of Health and Human Services","keywords":"Biology; Genetic architecture; Neuroscience; Evolutionary biology; Computational biology; Genetics; Cognitive science; Gene; Psychology; Phenotype","score_opus":0.005018011619853713,"score_gpt":0.26468171041825833,"score_spread":0.2596636987984046,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2980879969","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9993309,0.00010852889,0.00011577093,0.000021476908,0.0000015632316,0.000002302127,0.00017256514,0.0000031086795,0.00024387908],"genre_scores_gemma":[0.9994766,0.00005012472,0.00009599595,0.000010670611,0.0000026088185,0.0000038045387,0.00016641594,0.000002858684,0.00019103441],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9993254,0.00014333634,0.00006454048,0.00024777875,0.00010275526,0.00011608483],"domain_scores_gemma":[0.99932265,0.00020026947,0.00022934067,0.000076412594,0.00008086866,0.00009049866],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00044931416,0.0005422852,0.00046216854,0.0016682969,0.0007078322,0.00052546686,0.0006487939,0.0004924625,0.002281546],"category_scores_gemma":[0.0017540483,0.0005278574,0.000494541,0.0015120554,0.00061582716,0.00036243335,0.0005783629,0.00042767506,0.00018741837],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00019065305,0.00003635309,0.9922271,0.000011979166,0.0002624311,0.00096815184,0.00045150088,0.00019154497,0.0031326597,0.00022264785,0.00010117794,0.0022038901],"study_design_scores_gemma":[0.0000075381,0.00004727863,0.99821967,0.000003725038,0.000072337025,0.0009084593,0.000172085,0.0001946014,0.00013325957,0.0001584277,0.00007789792,0.0000047161698],"about_ca_topic_score_codex":0.016743502,"about_ca_topic_score_gemma":0.021715935,"teacher_disagreement_score":0.016743502,"about_ca_system_score_codex":0.00041458517,"about_ca_system_score_gemma":0.00036209385,"threshold_uncertainty_score":0.033292115},"labels":[],"label_agreement":null},{"id":"W2981875186","doi":"10.1038/s41588-019-0514-8","title":"HDAC9 is implicated in atherosclerotic aortic calcification and affects vascular smooth muscle cell phenotype","year":2019,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Connective tissue disorders research","field":"Biochemistry, Genetics and Molecular Biology","cited_by":146,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"McGill University Health Centre","funders":"National Center for Advancing Translational Sciences; National Institute on Minority Health and Health Disparities; National Center for Research Resources; National Institute of Diabetes and Digestive and Kidney Diseases; National Institute on Deafness and Other Communication Disorders; National Institute on Aging; National Institute of Neurological Disorders and Stroke; Bundesministerium für Bildung und Forschung; Heinz Nixdorf Stiftung; Deutsche Forschungsgemeinschaft; U.S. Department of Defense; Broad Institute; Kowa Company; School of Medicine, Boston University; American Heart Association; National Heart, Lung, and Blood Institute; Vetenskapsrådet; National Institutes of Health; U.S. Department of Health and Human Services; Hjartavernd; Fondation Leducq","keywords":"Calcification; Vascular smooth muscle; Biology; Contractility; Internal medicine; Genome-wide association study; Single-nucleotide polymorphism; Endocrinology; Medicine; Genetics; Gene; Smooth muscle; Genotype","score_opus":0.007934315300343052,"score_gpt":0.27130830873249706,"score_spread":0.263373993432154,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2981875186","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9823469,0.0046241,0.0052517015,0.00060328125,0.00030825526,0.000027739348,0.0019611514,0.00024366609,0.004633207],"genre_scores_gemma":[0.9939681,0.0008556862,0.0013235727,0.00012019949,0.000042819025,0.000009798451,0.00059082085,0.000059227008,0.0030296997],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9997111,0.000050214094,0.000033917506,0.00008308248,0.000080372934,0.000041244763],"domain_scores_gemma":[0.9997689,0.000036924583,0.000094184354,0.000027117592,0.000018168044,0.00005477659],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00022184261,0.000503691,0.000317339,0.0005408827,0.00028040473,0.0004050379,0.00046656822,0.00061271776,0.0045070704],"category_scores_gemma":[0.0002982549,0.0002940292,0.00044742992,0.00028503925,0.0003885242,0.00013498608,0.0002417785,0.00049884606,0.000854532],"study_design_candidate":"bench_or_experimental","study_design_consensus":"bench_or_experimental","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0007541579,0.00003904699,0.006076887,0.00007697881,0.00012812018,0.0014129623,0.000025285419,0.00013149522,0.9860626,0.00044776412,0.00031566847,0.004528932],"study_design_scores_gemma":[0.00027181214,0.0003539002,0.2217939,0.00005139035,0.00054252346,0.012585602,0.00016554506,0.0026069316,0.7461311,0.00092153635,0.014536745,0.000039054088],"about_ca_topic_score_codex":0.0011889073,"about_ca_topic_score_gemma":0.0021472303,"teacher_disagreement_score":0.0045070704,"about_ca_system_score_codex":0.00034089666,"about_ca_system_score_gemma":0.00015175654,"threshold_uncertainty_score":0.015077651},"labels":[],"label_agreement":null},{"id":"W2990909677","doi":"10.1038/s41588-019-0531-7","title":"Stalled developmental programs at the root of pediatric brain tumors","year":2019,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Chromatin Remodeling and Cancer","field":"Biochemistry, Genetics and Molecular Biology","cited_by":299,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"McGill Genome Centre; McGill University and Génome Québec Innovation Centre; Ontario Genomics; Hôpital Maisonneuve-Rosemont; Douglas Mental Health University Institute; Université Laval; University of Toronto; Université de Sherbrooke; Montreal Children's Hospital; Hospital for Sick Children; Université de Montréal; Centre Hospitalier Universitaire Sainte-Justine; Centre Hospitalier Universitaire de Sherbrooke; McGill University; McGill University Health Centre; SickKids Foundation; Montreal General Hospital; Jewish General Hospital","funders":"National Cancer Institute; Canadian Institutes of Health Research","keywords":"Biology; Wnt signaling pathway; Forebrain; Transcriptome; Lineage (genetic); Neuroectoderm; Embryonic stem cell; Subventricular zone; Neuroscience; Neural crest; Neural stem cell; Stem cell; Genetics; Central nervous system; Gene; Mesoderm; Gene expression","score_opus":0.005661622090003108,"score_gpt":0.24120663666211736,"score_spread":0.23554501457211424,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2990909677","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.94100964,0.015847456,0.020549206,0.004704774,0.00022978948,0.00004618536,0.0014631321,0.0018423148,0.014307586],"genre_scores_gemma":[0.9903532,0.00348716,0.0024735369,0.0002984564,0.000065773915,0.000016323092,0.00041463863,0.0001569644,0.002733901],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.999762,0.00002047175,0.0000110405535,0.00005358172,0.00007329469,0.00007951215],"domain_scores_gemma":[0.9993038,0.00013820316,0.00021989387,0.00006719944,0.00009692476,0.00017393926],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0003109637,0.00029539474,0.00041159062,0.00062519324,0.00042822398,0.0009358953,0.00046331208,0.00070013443,0.0029256789],"category_scores_gemma":[0.0009897683,0.00032440337,0.00016350258,0.00038900427,0.00072752434,0.00056646386,0.0008094716,0.0015498631,0.0008571498],"study_design_candidate":"bench_or_experimental","study_design_consensus":"bench_or_experimental","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0009008744,0.0000837131,0.040964812,0.0003068115,0.00008788583,0.008734431,0.0005889135,0.0064544952,0.787972,0.056691628,0.012173844,0.08504052],"study_design_scores_gemma":[0.00009817449,0.00035526938,0.20113745,0.00021549637,0.00015867037,0.015954461,0.0010241878,0.009631066,0.62602186,0.027936315,0.11738547,0.00008156248],"about_ca_topic_score_codex":0.0015980751,"about_ca_topic_score_gemma":0.00229741,"teacher_disagreement_score":0.0029256789,"about_ca_system_score_codex":0.0008291186,"about_ca_system_score_gemma":0.0009169211,"threshold_uncertainty_score":0.009787321},"labels":[],"label_agreement":null},{"id":"W2995367735","doi":"10.1038/s41588-019-0536-2","title":"Loss of ADAMTS19 causes progressive non-syndromic heart valve disease","year":2019,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Congenital heart defects research","field":"Biochemistry, Genetics and Molecular Biology","cited_by":66,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Toronto; Hospital for Sick Children; Université de Montréal; SickKids Foundation; Centre Hospitalier Universitaire Sainte-Justine","funders":"Fonds de Recherche du Québec - Santé; Fondation Leducq; Deutsche Forschungsgemeinschaft; Wellcome Trust; Wellcome; National Heart, Lung, and Blood Institute; Heart and Stroke Foundation of Canada","keywords":"Biology; Enhancer; Heart disease; Heart development; Transcription factor; Genetics; Internal medicine; Gene; Medicine; Embryonic stem cell","score_opus":0.006125347206483687,"score_gpt":0.2933975202395078,"score_spread":0.28727217303302416,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2995367735","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9959441,0.00037787258,0.001184256,0.00012689538,0.000047284168,0.00001436306,0.00029163522,0.000085507956,0.0019280959],"genre_scores_gemma":[0.9985287,0.00015653725,0.00049752276,0.000028262702,0.000030509038,0.0000030885144,0.00012451847,0.000017385315,0.00061345816],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99975735,0.000044510838,0.000039506012,0.000057073798,0.00007140241,0.000030254627],"domain_scores_gemma":[0.9994337,0.00022748986,0.00013269493,0.000044538712,0.000029313682,0.00013223446],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00015896161,0.0006540577,0.00030966848,0.00078305625,0.0002422229,0.00029009557,0.00036879457,0.0007297972,0.0025074696],"category_scores_gemma":[0.0007792246,0.00021512165,0.00031462536,0.00034570627,0.00047608936,0.00018019303,0.00040951086,0.00057504093,0.00043362903],"study_design_candidate":"bench_or_experimental","study_design_consensus":"bench_or_experimental","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0012280226,0.00027736946,0.04426972,0.00014535774,0.0002110172,0.25704154,0.00034975552,0.000692692,0.6745365,0.0012082376,0.0011907257,0.018849004],"study_design_scores_gemma":[0.00026426528,0.0012879611,0.32059938,0.000033405195,0.00028663382,0.5047692,0.00026809782,0.0028175812,0.1629632,0.0012981693,0.0053585656,0.00005350173],"about_ca_topic_score_codex":0.0003595119,"about_ca_topic_score_gemma":0.00042800236,"teacher_disagreement_score":0.0025074696,"about_ca_system_score_codex":0.00013235952,"about_ca_system_score_gemma":0.00013943517,"threshold_uncertainty_score":0.0083883405},"labels":[],"label_agreement":null},{"id":"W2995500161","doi":"10.1038/s41588-019-0552-2","title":"A call for global action for rare diseases in Africa","year":2019,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Genomics and Rare Diseases","field":"Biochemistry, Genetics and Molecular Biology","cited_by":66,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Children's Hospital of Eastern Ontario; University of Ottawa","funders":"Angela Wright Bennett Foundation; AveXis; Karolinska Institutet; African Union; Cambridge University Hospitals; Government of Western Australia; National Human Genome Research Institute; Amsterdam University Medical Centers; North-West University; McCusker Charitable Foundation; Curtin University of Technology; James Cook University; Universiteit van Amsterdam; National Institutes of Health; Common Fund; Istituto Superiore di Sanità; Keio University; University of Cambridge; African Union Commission; National Center for Advancing Translational Sciences; Medical Research Council; Pfizer; Universitat Pompeu Fabra; ACT Government","keywords":"Call to action; Orphan drug; Rare disease; Stakeholder; Global health; Public health; Action (physics); International Action; Stakeholder engagement; Economic growth; Biology; Public relations; Political science; Medicine; Business; Bioinformatics; Disease; Pathology","score_opus":0.008076999353402406,"score_gpt":0.26964367456706295,"score_spread":0.26156667521366056,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2995500161","genre_codex":"commentary","genre_gemma":"commentary","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"commentary","genre_consensus":"commentary","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.0012947888,0.018328425,0.0023867947,0.93159753,0.03926567,0.00004259684,0.00028127,0.00022338696,0.006579526],"genre_scores_gemma":[0.040878024,0.031077549,0.011534763,0.855533,0.03123399,0.00030051725,0.0006479205,0.00024299498,0.02855122],"study_design_codex":"not_applicable","study_design_gemma":"not_applicable","domain_scores_codex":[0.9913318,0.0024205863,0.00043527587,0.0007768335,0.0014910268,0.0035444673],"domain_scores_gemma":[0.94343543,0.015022855,0.002340622,0.0024461595,0.0061506596,0.030604227],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.022784555,0.0022259324,0.0021799991,0.0017590919,0.0034588054,0.005799972,0.0030876864,0.026569584,0.04484423],"category_scores_gemma":[0.025227105,0.00070750987,0.002772758,0.001109577,0.0074188197,0.010478342,0.015142343,0.026121216,0.006761436],"study_design_candidate":"not_applicable","study_design_consensus":"not_applicable","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00043736523,0.00027770814,0.0019925307,0.0020760132,0.00017180602,0.0014698944,0.0010251676,0.00052822917,0.0039553167,0.04017299,0.8534389,0.09445402],"study_design_scores_gemma":[0.00022631578,0.00019057973,0.0039556315,0.0014694831,0.00010931242,0.0006809118,0.0017226181,0.00018398114,0.00053060474,0.022289116,0.9685572,0.00008441775],"about_ca_topic_score_codex":0.0067351675,"about_ca_topic_score_gemma":0.0065297033,"teacher_disagreement_score":0.04484423,"about_ca_system_score_codex":0.0042332555,"about_ca_system_score_gemma":0.035815883,"threshold_uncertainty_score":0.15001893},"labels":[],"label_agreement":null},{"id":"W2997454792","doi":"10.1038/s41588-019-0559-8","title":"The Indian cobra reference genome and transcriptome enables comprehensive identification of venom toxins","year":2020,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Venomous Animal Envenomation and Studies","field":"Biochemistry, Genetics and Molecular Biology","cited_by":239,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Toronto","funders":"Genentech","keywords":"Biology; Cobra; Transcriptome; Identification (biology); Computational biology; Venom; Genome; Genetics; Gene; Gene expression; Computer science; Ecology","score_opus":0.016159008323217233,"score_gpt":0.2505940392311942,"score_spread":0.234435030907977,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2997454792","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.45937136,0.0053869626,0.113039546,0.0012431297,0.0003387319,0.00035596231,0.37271807,0.015199906,0.032346245],"genre_scores_gemma":[0.2961343,0.0025686037,0.091812864,0.00029218727,0.00007227057,0.00033815764,0.59900254,0.0022756772,0.0075034355],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.99952364,0.000043172862,0.000035119647,0.00020084342,0.000118282645,0.00007886344],"domain_scores_gemma":[0.99938,0.00008753942,0.0001242321,0.00013948341,0.00018061051,0.00008810417],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00034066424,0.00086478336,0.00082498585,0.0020852338,0.0014810129,0.0011933668,0.0008169295,0.00072324916,0.0042250184],"category_scores_gemma":[0.001053044,0.00046629456,0.0010371207,0.0034455897,0.00031817422,0.0004904411,0.0009440118,0.0012952733,0.003579156],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0012158446,0.00012807686,0.009599982,0.0012758126,0.0001631656,0.0007214978,0.00063526153,0.0026860775,0.91326565,0.0022337162,0.01643892,0.051635917],"study_design_scores_gemma":[0.00016983601,0.0004606346,0.29974517,0.000548721,0.0011537471,0.0034550827,0.0006411125,0.012078432,0.17844228,0.0029500907,0.50010747,0.0002474191],"about_ca_topic_score_codex":0.01277675,"about_ca_topic_score_gemma":0.025785914,"teacher_disagreement_score":0.01277675,"about_ca_system_score_codex":0.0007053276,"about_ca_system_score_gemma":0.0015150914,"threshold_uncertainty_score":0.02540481},"labels":[],"label_agreement":null},{"id":"W2999027176","doi":"10.1038/s41588-019-0566-9","title":"Transcription phenotypes of pancreatic cancer are driven by genomic events during tumor evolution","year":2020,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Pancreatic and Hepatic Oncology Research","field":"Medicine","cited_by":689,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"McGill University Health Centre; Canada's Michael Smith Genome Sciences Centre; University of British Columbia; Pancreas Centre (Canada); Vancouver General Hospital; Lunenfeld-Tanenbaum Research Institute; Mount Sinai Hospital; University of Toronto; University Health Network; Princess Margaret Cancer Centre; Ontario Institute for Cancer Research","funders":"","keywords":"Biology; Transcriptome; KRAS; Pancreatic cancer; Genetics; Genome instability; Genetic heterogeneity; Chromothripsis; Phenotype; Genome; Gene; Tumor progression; Comparative genomic hybridization; Chromosome instability; Computational biology; Cancer; Mutation; Gene expression; DNA; Chromosome","score_opus":0.01687609019782679,"score_gpt":0.3000861783805061,"score_spread":0.28321008818267934,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2999027176","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9901764,0.00080065225,0.004567303,0.00030412033,0.00002726802,0.000009053882,0.0007424958,0.00011345737,0.0032592781],"genre_scores_gemma":[0.9967404,0.0003585376,0.0007823463,0.000106290616,0.000012422573,0.000009180644,0.0005735311,0.00006341505,0.0013538193],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9998011,0.000034825815,0.000010064874,0.00006112406,0.000042544325,0.00005036903],"domain_scores_gemma":[0.99978477,0.00006446371,0.000055831213,0.000032279273,0.000021911683,0.000040834486],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00019106858,0.00019793399,0.00019757441,0.0003631536,0.00019664915,0.0005822179,0.00017598218,0.00027978144,0.0017469074],"category_scores_gemma":[0.000341504,0.00022496739,0.00022449427,0.00032075695,0.00035672725,0.00025957765,0.0005410023,0.00069055264,0.00041569085],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0002856717,0.000010944505,0.010886347,0.000026617543,0.000011881485,0.00017551285,0.000102675716,0.00037308203,0.9833323,0.0008944734,0.00014966223,0.0037508681],"study_design_scores_gemma":[0.000040401734,0.00021682681,0.47366905,0.000028827344,0.000050310126,0.0017432165,0.00064419495,0.0048737284,0.50764185,0.0022204993,0.008831158,0.000039921175],"about_ca_topic_score_codex":0.0007718207,"about_ca_topic_score_gemma":0.0015675582,"teacher_disagreement_score":0.0017469074,"about_ca_system_score_codex":0.00040195667,"about_ca_system_score_gemma":0.00017182398,"threshold_uncertainty_score":0.0058439374},"labels":[],"label_agreement":null},{"id":"W2999883126","doi":"10.1038/s41588-019-0537-1","title":"Fine-mapping of 150 breast cancer risk regions identifies 191 likely target genes","year":2020,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Bioinformatics and Genomic Networks","field":"Biochemistry, Genetics and Molecular Biology","cited_by":189,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of British Columbia; University Health Network; Université Laval; Centre Hospitalier de l’Université de Montréal; Simon Fraser University; McGill University; Queen's University; Women's College Hospital; Centre hospitalier universitaire de Québec; Royal Victoria Hospital; University of Toronto; Lunenfeld-Tanenbaum Research Institute; Mount Sinai Hospital; BC Cancer Agency","funders":"National Center for Advancing Translational Sciences; National Cancer Institute; Biocenter, University of Oulu; Det Sundhedsvidenskabelige Fakultet, Københavns Universitet; BC Cancer Agency; Russian Academy of Sciences; National Medical Research Council; Medical Research Council; Horizon 2020 Framework Programme; University of California, San Francisco; University of North Carolina at Chapel Hill; University of Texas MD Anderson Cancer Center; National Institute of Mental Health; School of Medicine, Vanderbilt University; National Institutes of Health; Centre Léon Bérard; Centro de Investigación Biomédica en Red de Cáncer; National Institute of General Medical Sciences; Deutschen Konsortium für Translationale Krebsforschung; Skånes universitetssjukhus; Universidad de La Sabana; Pomorski Uniwersytet Medyczny W Szczecinie; Institut Gustave-Roussy; Ministero dello Sviluppo Economico; Agence Nationale de Sécurité Sanitaire de l’Alimentation, de l’Environnement et du Travail; Uppsala Universitet; Universidade do Porto; Universitetssjukhuset Örebro; Umm Al-Qura University; Biomedical Research Council; Federal Agency for Scientific Organizations; Clalit Health Services; Lineberger Comprehensive Cancer Center, University of North Carolina at Chapel Hill; Hospices Civils de Lyon; Aalborg Universitetshospital; Medizinischen Hochschule Hannover; Kuopion Yliopistollinen Sairaala; Université Paris Descartes; University of Nottingham; Universitetet i Oslo; Oak Foundation; Leids Universitair Medisch Centrum; Simon Fraser University; Peter MacCallum Cancer Centre; Odense Universitetshospital; Servicio Gallego de Salud; Institut Bergonié; Great Ormond Street Hospital for Children; Örebro Universitet; Queen's University; University of California, Irvine; Oulun Yliopisto; Universität Wien; Japan Agency for Medical Research and Development; Curtin University of Technology; Deutsche Gesetzliche Unfallversicherung; King's College London; Imperial College London; Gentofte Hospital; Aalborg Universitet; Cancer Australia; Russian Foundation for Basic Research; National Health and Medical Research Council; Deutsche Krebshilfe; Academia Sinica; Monash University; Institut National de la Santé et de la Recherche Médicale; University of Westminster; Wellcome Trust; Agence Nationale de la Recherche; Medisinske fakultet, Universitetet i Oslo; Hunter Medical Research Institute; Nottingham University Hospitals NHS Trust; National Breast Cancer Foundation; Queen's University Belfast; China Medical University; Itä-Suomen Yliopisto; Eberhard Karls Universität Tübingen; Ohio State University; Universiteit Leiden; University of Chicago; University of Glasgow; Deutsches Krebsforschungszentrum; University of Aberdeen; Canadian Institutes of Health Research; European Commission; Lon V. Smith Foundation; University of Oxford; University of Toronto; Government of Canada; National Institute of Environmental Health Sciences; Universiti Malaya; Swedish Cancer Foundation; Centre Hospitalier Universitaire de Québec; V Foundation for Cancer Research; NRG Oncology; Vanderbilt University; University Hospitals of Leicester NHS Trust; Rigshospitalet; Ministère du Développement Économique, de l’Innovation et de l’Exportation; University College London; Cancer Research UK; Istituto Oncologico Veneto; Institut National Du Cancer; Memorial Sloan-Kettering Cancer Center; Fondation du cancer du sein du Québec; Institute of Biomedical Sciences, Academia Sinica; David F. and Margaret T. Grohne Family Foundation; National Institute for Health and Care Research; Karolinska Institutet; Universitätsklinikum Hamburg-Eppendorf; Vanderbilt-Ingram Cancer Center; Yale University; Harvard T.H. Chan School of Public Health; Helsingin ja Uudenmaan Sairaanhoitopiiri; Breast Cancer Research Foundation; University of Pretoria; University of New South Wales; University of Pittsburgh; Fondazione Italiana per la Ricerca sul Cancro; Royal Marsden NHS Foundation Trust; Université Laval; Helsingin Yliopisto; Mailman School of Public Health, Columbia University; Universität Heidelberg; UK Dementia Research Institute; Taiwan Biobank; Pontificia Universidad Javeriana; University of Wisconsin-Milwaukee; Cancer Research Institute; Medizinische Universität Wien; Canada's Michael Smith Genome Sciences Centre; Klinisk Institut, Aalborg Universitet; Genome Canada; Brigham and Women's Hospital; Instituto de Investigación Sanitaria de Santiago de Compostela; ACT Government; University of Melbourne; Institut Claudius Regaud; California Department of Public Health; U.S. Department of Health and Human Services; Huntsman Cancer Institute; Health Sciences Center, University of New Mexico; Háskóli Íslands; NIHR Oxford Biomedical Research Centre; Landspítali Háskólasjúkrahús; Ministerio de Economía y Competitividad; Ministry of Education, Culture, Sports, Science and Technology; Ovarian Cancer Research Fund; Faculty of Health and Medical Sciences, University of Western Australia; Lunds Universitet; QIMR Berghofer Medical Research Institute; Fundación Cellex","keywords":"Biology; Genetics; Computational biology; Gene; Linkage disequilibrium; Expression quantitative trait loci; Genome-wide association study; Genetic association; Single-nucleotide polymorphism; Allele; Haplotype; Genotype","score_opus":0.007833456764252785,"score_gpt":0.23148608869019913,"score_spread":0.22365263192594634,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2999883126","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9698593,0.0022743966,0.01558476,0.00025019186,0.000022703029,0.000055497825,0.0071953866,0.00039424343,0.0043636295],"genre_scores_gemma":[0.9849017,0.0004731853,0.007481322,0.00020945689,0.000012790596,0.00003507209,0.005489538,0.00006168895,0.0013353062],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9997609,0.00003258613,0.000013348041,0.0000960326,0.000057707577,0.0000394005],"domain_scores_gemma":[0.9993137,0.0004711565,0.00007472395,0.00006534249,0.000029087894,0.00004608683],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00029617164,0.0002565166,0.0005858302,0.00073660293,0.00029720066,0.0003943662,0.00035962928,0.000420356,0.0044456776],"category_scores_gemma":[0.00088663073,0.00022532286,0.0008016389,0.0007776416,0.00018720923,0.00010960711,0.00031069788,0.0003385491,0.0012114634],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0017951082,0.000197223,0.16330092,0.00053329236,0.0005150338,0.0022881574,0.00019725758,0.0065223514,0.714163,0.0019253456,0.00290979,0.10565258],"study_design_scores_gemma":[0.00030297146,0.00041402143,0.8349479,0.000057131907,0.0009222373,0.003971999,0.0001447169,0.014170273,0.11977626,0.0043911235,0.020848298,0.000053076146],"about_ca_topic_score_codex":0.0021186653,"about_ca_topic_score_gemma":0.0044573382,"teacher_disagreement_score":0.0044456776,"about_ca_system_score_codex":0.00027323668,"about_ca_system_score_gemma":0.00026103796,"threshold_uncertainty_score":0.014872253},"labels":[],"label_agreement":null},{"id":"W3004613412","doi":"10.1038/s41588-019-0564-y","title":"Disruption of chromatin folding domains by somatic genomic rearrangements in human cancer","year":2020,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Genomics and Chromatin Dynamics","field":"Biochemistry, Genetics and Molecular Biology","cited_by":308,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"SickKids Foundation; BC Cancer Agency; University of British Columbia; Prostate Cancer Canada; Université de Montréal; Hospital for Sick Children; Simon Fraser University; University of Ottawa; McGill University; Lunenfeld-Tanenbaum Research Institute; Mount Sinai Hospital; Princess Margaret Cancer Centre; University of Calgary; University of Toronto; McGill University and Génome Québec Innovation Centre; Toronto General Hospital; University Health Network; Genome Canada; Canada's Michael Smith Genome Sciences Centre; Vector Institute; Institute of Cancer Research; Ontario Institute for Cancer Research","funders":"National Institute of Environmental Health Sciences; National Institute of General Medical Sciences; National Cancer Institute; National Institutes of Health; Cancer Research UK; Emerson Collective; Francis Crick Institute; Cancer Prevention and Research Institute of Texas; Welch Foundation","keywords":"Chromatin; Biology; Genome; Computational biology; Histone; Somatic cell; Gene; Genetics; Human genome; Cancer","score_opus":0.006746878620244802,"score_gpt":0.2635187199234098,"score_spread":0.256771841303165,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W3004613412","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99792755,0.00030323246,0.0011502336,0.000012939023,0.0000019915299,0.0000061665573,0.00034020134,0.000027244167,0.0002302684],"genre_scores_gemma":[0.99846244,0.00012329221,0.0008967455,0.0000201982,0.0000010588763,0.0000049564233,0.00037287967,0.0000085164165,0.000109815555],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9998697,0.000022840872,0.0000104016935,0.000039241728,0.00003429053,0.000023459943],"domain_scores_gemma":[0.9998722,0.000030770258,0.0000542193,0.000019533269,0.00000891847,0.000014305599],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00013310334,0.00009756559,0.00018668694,0.00056796573,0.00016093007,0.00016883055,0.00008630364,0.000167363,0.0004865816],"category_scores_gemma":[0.00030943443,0.00012209598,0.00019676413,0.00090460834,0.00016830447,0.00008024946,0.00018894351,0.00019165393,0.000108407476],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00067565544,0.00005561637,0.12796423,0.00009392824,0.00019172637,0.0005584829,0.00018453115,0.0038916082,0.8445143,0.00059239264,0.0002220333,0.021055548],"study_design_scores_gemma":[0.000028739061,0.00031281236,0.7877641,0.000014955628,0.00013347896,0.0040766452,0.00018629475,0.010272782,0.19272478,0.0011317596,0.0033319413,0.00002173312],"about_ca_topic_score_codex":0.0010997059,"about_ca_topic_score_gemma":0.0023770968,"teacher_disagreement_score":0.0010997059,"about_ca_system_score_codex":0.0001993507,"about_ca_system_score_gemma":0.00010107864,"threshold_uncertainty_score":0.0021865964},"labels":[],"label_agreement":null},{"id":"W3005218670","doi":"10.1038/s41588-019-0562-0","title":"Pan-cancer analysis of whole genomes identifies driver rearrangements promoted by LINE-1 retrotransposition","year":2020,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Chromosomal and Genetic Variations","field":"Agricultural and Biological Sciences","cited_by":478,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Ottawa; University of Toronto; Ontario Institute for Cancer Research; McGill University","funders":"National Institute of Environmental Health Sciences; National Cancer Institute; National Human Genome Research Institute; National Institute for Health and Care Research; National Institute on Aging; Medical Research Council; Imperial Experimental Cancer Medicine Centre; Vlaamse regering; Ministerio de Asuntos Económicos y Transformación Digital, Gobierno de España; Fonds Wetenschappelijk Onderzoek; Società Italiana di Ematologia Sperimentale; Li Ka Shing Foundation; European Commission; Wellcome Trust; Cancer Research UK; National Institutes of Health; Agencia Estatal de Investigación; Schweizerischer Nationalfonds zur Förderung der Wissenschaftlichen Forschung; Xunta de Galicia; National Institute of General Medical Sciences; Centres de Recerca de Catalunya; Francis Crick Institute; Associazione Italiana Contro le Leucemie-Linfomi e Mieloma; Sundhed og Sygdom, Det Frie Forskningsråd; Korea Health Industry Development Institute; Associazione Italiana per la Ricerca sul Cancro; American Heart Association","keywords":"Biology; Retrotransposon; Genome; Genetics; Computational biology; Line (geometry); Evolutionary biology; Gene; Transposable element","score_opus":0.015062402708120816,"score_gpt":0.24537573851068525,"score_spread":0.23031333580256444,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W3005218670","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9935104,0.0009695173,0.0029969998,0.00002454499,0.000003076702,0.000011621576,0.0018576913,0.00006521704,0.00056094455],"genre_scores_gemma":[0.9938176,0.00040527392,0.0025724114,0.0000270448,0.0000029171222,0.000010262622,0.0027975373,0.000024796696,0.0003420391],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.99976426,0.000030903622,0.000014776956,0.00010119485,0.00004776834,0.000041076357],"domain_scores_gemma":[0.9996898,0.00008521248,0.00012568403,0.00003444603,0.000027695934,0.000037136157],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00021399384,0.00020310603,0.00020426293,0.0010125668,0.00021155087,0.00034589894,0.0001405821,0.00022012877,0.001235981],"category_scores_gemma":[0.00054408726,0.00012416436,0.0001986036,0.0009679054,0.00016420768,0.00018299875,0.00031469256,0.00021607608,0.00017614974],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.000519318,0.000029915167,0.39006537,0.00021447666,0.00026569585,0.00037837256,0.00024160837,0.00061823765,0.5750715,0.0003282906,0.00020844566,0.03205887],"study_design_scores_gemma":[0.000010827633,0.00013443972,0.9355648,0.000015430376,0.00015210439,0.0021629643,0.0001651487,0.0017371604,0.055507354,0.00027715715,0.0042624795,0.000010084757],"about_ca_topic_score_codex":0.0010239722,"about_ca_topic_score_gemma":0.0029217936,"teacher_disagreement_score":0.001235981,"about_ca_system_score_codex":0.00016160002,"about_ca_system_score_gemma":0.00015308404,"threshold_uncertainty_score":0.004134834},"labels":[],"label_agreement":null},{"id":"W3005400930","doi":"10.1038/s41588-019-0558-9","title":"The landscape of viral associations in human cancers","year":2020,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Viral-associated cancers and disorders","field":"Medicine","cited_by":403,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"SickKids Foundation; BC Cancer Agency; University of British Columbia; Prostate Cancer Canada; Simon Fraser University; University of Ottawa; McGill University; Lunenfeld-Tanenbaum Research Institute; Mount Sinai Hospital; Princess Margaret Cancer Centre; University of Calgary; Vector Institute; University of Toronto; McGill University and Génome Québec Innovation Centre; Toronto General Hospital; University Health Network; Genome Canada; Canada's Michael Smith Genome Sciences Centre; Hospital for Sick Children; Université de Montréal; Institute of Cancer Research; Ontario Institute for Cancer Research","funders":"Leibniz-Institut für Naturstoff-Forschung und Infektionsbiologie – Hans-Knöll-Institut; National Institute of Environmental Health Sciences; National Cancer Institute; Biotechnology and Biological Sciences Research Council; Bundesministerium für Bildung und Forschung; Schweizerischer Nationalfonds zur Förderung der Wissenschaftlichen Forschung; Leibniz-Gemeinschaft; Government of Ontario; Cancer Research UK; National Science Foundation; Ontario Institute for Cancer Research; Deutsches Zentrum für Infektionsforschung; Deutsches Krebsforschungszentrum; Francis Crick Institute","keywords":"Biology; APOBEC; Transcriptome; Hepatitis B virus; Genome; Virology; Virus; Cancer; Merkel cell polyomavirus; Endogenous retrovirus; Genetics; Gene; Cancer research; Carcinoma; Merkel cell carcinoma; Gene expression","score_opus":0.009924264291170564,"score_gpt":0.2819074765132694,"score_spread":0.27198321222209887,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W3005400930","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9175495,0.042000983,0.017711364,0.0014145493,0.00007685217,0.00004961812,0.016801625,0.0003131301,0.004082349],"genre_scores_gemma":[0.9675242,0.007849732,0.008222627,0.000582307,0.00007235378,0.00006275915,0.014765937,0.00016273874,0.0007574],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99858403,0.00035925215,0.0000743819,0.0006513423,0.00021547863,0.000115514405],"domain_scores_gemma":[0.9987256,0.0005867459,0.00030467293,0.00015639202,0.00012581334,0.00010074823],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0011636602,0.00027562893,0.00059300323,0.0019848316,0.0005283114,0.0018191532,0.0002525455,0.00043639287,0.0014703416],"category_scores_gemma":[0.00291417,0.00026403688,0.0005308373,0.0023662637,0.00039096895,0.0006728772,0.0011272555,0.0005528756,0.00039667802],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00057214353,0.000052135438,0.79912776,0.0012929908,0.0017310272,0.00054054044,0.0007587181,0.005983677,0.078823775,0.0050074034,0.0036968684,0.102413036],"study_design_scores_gemma":[0.000031065538,0.00019030331,0.8897538,0.00035405377,0.00086377934,0.0024599037,0.0013648212,0.013987523,0.01101596,0.02407185,0.055823795,0.00008312388],"about_ca_topic_score_codex":0.0017272984,"about_ca_topic_score_gemma":0.0038303526,"teacher_disagreement_score":0.0019848316,"about_ca_system_score_codex":0.00047916453,"about_ca_system_score_gemma":0.0005211888,"threshold_uncertainty_score":0.00615412},"labels":[],"label_agreement":null},{"id":"W3005469082","doi":"10.1038/s41588-019-0576-7","title":"Comprehensive analysis of chromothripsis in 2,658 human cancers using whole-genome sequencing","year":2020,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Genomic variations and chromosomal abnormalities","field":"Biochemistry, Genetics and Molecular Biology","cited_by":774,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"SickKids Foundation; BC Cancer Agency; University of British Columbia; Prostate Cancer Canada; Université de Montréal; Hospital for Sick Children; Simon Fraser University; University of Ottawa; McGill University; Lunenfeld-Tanenbaum Research Institute; Mount Sinai Hospital; Princess Margaret Cancer Centre; University of Calgary; McGill University and Génome Québec Innovation Centre; Toronto General Hospital; University of Toronto; University Health Network; Genome Canada; Canada's Michael Smith Genome Sciences Centre; Vector Institute; Institute of Cancer Research; Ontario Institute for Cancer Research","funders":"National Institute of General Medical Sciences; National Cancer Institute; National Institutes of Health; Cancer Research UK; Ludwig Center at Harvard; European Commission; Francis Crick Institute","keywords":"Chromothripsis; Biology; Genome; Genetics; Cancer; Human genome; Computational biology; Gene; Genome instability; DNA","score_opus":0.025258840331190628,"score_gpt":0.27504643217011226,"score_spread":0.24978759183892163,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W3005469082","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9781001,0.0026220996,0.0052032173,0.00009165747,0.000012271813,0.000045859495,0.012627382,0.00016069246,0.0011366839],"genre_scores_gemma":[0.9624128,0.0018582515,0.009209186,0.00012718295,0.000016930611,0.000060760456,0.025111033,0.00008580635,0.0011180291],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.99972075,0.000021859561,0.000021601058,0.000116956995,0.00008159683,0.00003717848],"domain_scores_gemma":[0.9996674,0.000097753014,0.000074515025,0.000046676847,0.00005089262,0.00006284412],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00034921497,0.00031040565,0.00033686077,0.0013456745,0.00033024905,0.0003301203,0.00019451893,0.00028005207,0.00065229693],"category_scores_gemma":[0.00066864403,0.00018751239,0.00036523538,0.0015241259,0.00016864343,0.000107785505,0.00041024483,0.00027313904,0.00021756765],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0005321426,0.000050563947,0.28217092,0.00052071875,0.0009979609,0.0014286967,0.00042382308,0.0017558578,0.6407129,0.0004378799,0.002186228,0.06878234],"study_design_scores_gemma":[0.000022999859,0.000084994084,0.9668327,0.000025573254,0.00031490353,0.0018716138,0.00009230966,0.0014623859,0.020346228,0.0003278675,0.008601889,0.00001654016],"about_ca_topic_score_codex":0.0032607117,"about_ca_topic_score_gemma":0.009788409,"teacher_disagreement_score":0.0032607117,"about_ca_system_score_codex":0.00021045741,"about_ca_system_score_gemma":0.00030927281,"threshold_uncertainty_score":0.0064834356},"labels":[],"label_agreement":null},{"id":"W3005574610","doi":"10.1038/s41588-020-0588-3","title":"Author Correction: Transcription phenotypes of pancreatic cancer are driven by genomic events during tumor evolution","year":2020,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Cancer Genomics and Diagnostics","field":"Biochemistry, Genetics and Molecular Biology","cited_by":19,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"McGill University Health Centre; Canada's Michael Smith Genome Sciences Centre; University of British Columbia; Pancreas Centre (Canada); Vancouver General Hospital; Lunenfeld-Tanenbaum Research Institute; Mount Sinai Hospital; University of Toronto; University Health Network; Princess Margaret Cancer Centre; Ontario Institute for Cancer Research","funders":"","keywords":"Biology; Pancreatic cancer; Phenotype; Genetics; Computational biology; Transcription (linguistics); Evolutionary biology; Gene; Cancer","score_opus":0.0061863588830226735,"score_gpt":0.2313730519771455,"score_spread":0.22518669309412281,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W3005574610","genre_codex":"editorial","genre_gemma":"other","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"other","genre_consensus":null,"domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.0015081594,0.0008060707,0.0035057953,0.060314577,0.9283912,0.000028807208,0.0019127488,0.0012357782,0.0022969255],"genre_scores_gemma":[0.19470379,0.00887462,0.029399127,0.111597344,0.2891343,0.0004436978,0.009879929,0.008053503,0.3479137],"study_design_codex":"not_applicable","study_design_gemma":"not_applicable","domain_scores_codex":[0.9954462,0.0005995286,0.00064137345,0.0009007616,0.0018987254,0.00051338854],"domain_scores_gemma":[0.9756128,0.006671787,0.0017874041,0.0025960386,0.011137375,0.002194581],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0034443685,0.0015384796,0.0019216852,0.00199525,0.0027586087,0.003084151,0.003786305,0.0072961715,0.057657562],"category_scores_gemma":[0.040501595,0.0011298115,0.00148926,0.0020084355,0.0023385633,0.0018697485,0.0024093988,0.009510871,0.02348414],"study_design_candidate":"not_applicable","study_design_consensus":"not_applicable","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00015361037,0.000015696463,0.0006057214,0.0003591773,0.00008581244,0.0021577475,0.000111042566,0.00024539614,0.0014271644,0.0025482578,0.9814476,0.0108428495],"study_design_scores_gemma":[0.00016877176,0.000054696055,0.0028202336,0.0002656315,0.00016304421,0.005744525,0.00026041025,0.0014138608,0.0058621517,0.00339214,0.97975886,0.0000955853],"about_ca_topic_score_codex":0.0053353193,"about_ca_topic_score_gemma":0.006839106,"teacher_disagreement_score":0.057657562,"about_ca_system_score_codex":0.00310812,"about_ca_system_score_gemma":0.004076113,"threshold_uncertainty_score":0.19288379},"labels":[],"label_agreement":null},{"id":"W3005905327","doi":"10.1038/s41588-019-0575-8","title":"A slipped-CAG DNA-binding small molecule induces trinucleotide-repeat contractions in vivo","year":2020,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Genetic Neurodegenerative Diseases","field":"Neuroscience","cited_by":147,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Toronto; SickKids Foundation; Université Laval; Hospital for Sick Children","funders":"National Institute of Environmental Health Sciences; National Human Genome Research Institute; Cancer Research UK","keywords":"Trinucleotide repeat expansion; Biology; DNA; Striatum; Mutant; Huntington's disease; In vivo; Transcription (linguistics); DNA repair; DNA replication; Cell biology; Genetics; Molecular biology; Transcription factor; Allele; Gene; Internal medicine; Endocrinology; Disease","score_opus":0.03531100015798447,"score_gpt":0.2762495722802551,"score_spread":0.24093857212227063,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W3005905327","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9920108,0.0007548082,0.004243224,0.00013524758,0.000086405795,0.000054597567,0.00017757744,0.00016336968,0.0023739194],"genre_scores_gemma":[0.9902429,0.00040847686,0.0041369456,0.0001242013,0.000031615604,0.00007380118,0.00071793376,0.0001186536,0.0041454695],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9997888,0.00004191196,0.000014680791,0.000063497,0.000048020273,0.00004313291],"domain_scores_gemma":[0.99953127,0.00019864934,0.00008784422,0.000053606866,0.000018636008,0.000110039684],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0003759509,0.0003984618,0.0003520254,0.00028681633,0.00021491725,0.0002620831,0.00041444905,0.0005409649,0.0027322748],"category_scores_gemma":[0.00027456667,0.0002930997,0.0002750839,0.00013862291,0.00035571115,0.00014640894,0.00033490188,0.0009142917,0.00060233317],"study_design_candidate":"bench_or_experimental","study_design_consensus":"bench_or_experimental","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00006917035,0.00002066238,0.000031255368,0.00000800873,0.0000031283387,0.00002388702,0.0000040880022,0.000026051335,0.9994598,0.000045229113,0.000021827029,0.00028684209],"study_design_scores_gemma":[0.000029835868,0.00026611978,0.0008967969,0.0000032540784,0.000005761238,0.00011240658,0.000006508588,0.0006610648,0.9972416,0.000025645935,0.0007476622,0.0000032894486],"about_ca_topic_score_codex":0.00064560183,"about_ca_topic_score_gemma":0.0010329545,"teacher_disagreement_score":0.0027322748,"about_ca_system_score_codex":0.00033235483,"about_ca_system_score_gemma":0.00028751092,"threshold_uncertainty_score":0.009140372},"labels":[],"label_agreement":null},{"id":"W3008130095","doi":"10.1038/s41588-020-0589-2","title":"Author Correction: Human somatic cell mutagenesis creates genetically tractable sarcomas","year":2020,"lang":"en","type":"erratum","venue":"Nature Genetics","topic":"Animal Genetics and Reproduction","field":"Biochemistry, Genetics and Molecular Biology","cited_by":0,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Mount Sinai Hospital; University of Toronto; Ontario Institute for Cancer Research","funders":"","keywords":"Biology; Somatic cell; Mutagenesis; Computational biology; Genetically engineered; Genetics; Mutation; Gene","score_opus":0.010034229559490137,"score_gpt":0.2608838164294539,"score_spread":0.2508495868699638,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W3008130095","genre_codex":"editorial","genre_gemma":"other","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"other","genre_consensus":null,"domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.0013249427,0.0010578142,0.0059015024,0.03822965,0.93197954,0.000044431617,0.0036859356,0.0013573191,0.016418777],"genre_scores_gemma":[0.03701845,0.0060101002,0.023144677,0.035964526,0.06461969,0.00019194372,0.008026328,0.0043654037,0.8206589],"study_design_codex":"not_applicable","study_design_gemma":"not_applicable","domain_scores_codex":[0.9980457,0.00020017115,0.00022551097,0.00025557494,0.0011103088,0.00016282088],"domain_scores_gemma":[0.9902868,0.0023810938,0.00043625457,0.00089275005,0.0053181825,0.00068490434],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.002304896,0.0013279016,0.0010299516,0.0018368443,0.002213834,0.0020481874,0.00245869,0.004590919,0.071339585],"category_scores_gemma":[0.015208633,0.00079717726,0.00087288645,0.0011137876,0.001251238,0.0013295074,0.0012734885,0.00631213,0.028452296],"study_design_candidate":"not_applicable","study_design_consensus":"not_applicable","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.000073971736,0.000014679215,0.0001546091,0.00013192421,0.000018270914,0.0012966056,0.000035055724,0.00016688844,0.00077822234,0.0026506067,0.9808977,0.013781428],"study_design_scores_gemma":[0.000042950123,0.0000158471,0.0005382869,0.000107806416,0.000042407577,0.0018027424,0.00004102283,0.0003638947,0.0028523407,0.0015773887,0.99258375,0.000031648422],"about_ca_topic_score_codex":0.010019079,"about_ca_topic_score_gemma":0.01546719,"teacher_disagreement_score":0.071339585,"about_ca_system_score_codex":0.0022970112,"about_ca_system_score_gemma":0.0029811973,"threshold_uncertainty_score":0.23865467},"labels":[],"label_agreement":null},{"id":"W3012672248","doi":"10.1038/s41588-020-0606-5","title":"Establishing the International Genetic Discrimination Observatory","year":2020,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Ethics in Clinical Research","field":"Medicine","cited_by":28,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Toronto; McGill University","funders":"Novo Nordisk Fonden; Government of Canada; NordForsk; Novo Nordisk; Canadian Institutes of Health Research; Genome Canada","keywords":"Biology; Genetic discrimination; Observatory; Genetics; Human genetics; Evolutionary biology; Engineering ethics; Computational biology; Genetic testing; Gene; Engineering","score_opus":0.3316106810151291,"score_gpt":0.5036652365617759,"score_spread":0.17205455554664678,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W3012672248","genre_codex":"commentary","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":null,"domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.030846221,0.0022074843,0.028635904,0.76750886,0.018881759,0.00052332284,0.00018108422,0.00028370577,0.15093161],"genre_scores_gemma":[0.54903096,0.0011764113,0.04682584,0.29506,0.0077880654,0.001131539,0.00031483916,0.0003622826,0.09831011],"study_design_codex":"theoretical_or_conceptual","study_design_gemma":"not_applicable","domain_scores_codex":[0.9419139,0.01892191,0.003453445,0.006507922,0.014832188,0.014370677],"domain_scores_gemma":[0.83781075,0.0549545,0.010467391,0.017391007,0.020977406,0.05839896],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.13723615,0.0005852222,0.0008388206,0.0018503467,0.009957268,0.014585722,0.0024004963,0.022153938,0.0069398507],"category_scores_gemma":[0.13049142,0.0010970194,0.0010183481,0.0010101844,0.014531017,0.009837238,0.02323067,0.044873834,0.0014530731],"study_design_candidate":"not_applicable","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00010479949,0.00029820122,0.009843331,0.00010950533,0.000032117874,0.00075520715,0.0066508637,0.00035744463,0.0021231887,0.8180169,0.12522493,0.03648337],"study_design_scores_gemma":[0.00013482264,0.00017020032,0.011266954,0.0006573059,0.000040081468,0.00040055503,0.0047058016,0.0010817616,0.0019634238,0.2083077,0.7711317,0.00013983378],"about_ca_topic_score_codex":0.008190617,"about_ca_topic_score_gemma":0.011154144,"teacher_disagreement_score":0.13723615,"about_ca_system_score_codex":0.008416662,"about_ca_system_score_gemma":0.07648867,"threshold_uncertainty_score":0.72578275},"labels":[],"label_agreement":null},{"id":"W3012749684","doi":"10.1038/s41588-020-0592-7","title":"Genomic characterization of human brain metastases identifies drivers of metastatic lung adenocarcinoma","year":2020,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Cancer Genomics and Diagnostics","field":"Biochemistry, Genetics and Molecular Biology","cited_by":302,"is_retracted":false,"has_abstract":false,"route_ca_aff":false,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"","funders":"Canadian Institutes of Health Research; Breast Cancer Research Foundation; American Brain Tumor Association; Damon Runyon Cancer Research Foundation; Brain Science Foundation; National Cancer Institute; Government of Canada; U.S. Department of Health and Human Services","keywords":"CDKN2A; Brain metastasis; Biology; Adenocarcinoma; Exome sequencing; Metastasis; Cancer research; Lung; Oncology; Cancer; Internal medicine; Gene; Genetics; Medicine; Mutation","score_opus":0.009847977823237677,"score_gpt":0.2565374810280105,"score_spread":0.24668950320477281,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W3012749684","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99323773,0.00067656,0.0023055759,0.00014915153,0.0000082369415,0.000019041356,0.0016620834,0.00007773768,0.0018637392],"genre_scores_gemma":[0.9968292,0.00036078886,0.0008438383,0.000042571097,0.0000058604883,0.000009606943,0.0011200554,0.000032623087,0.00075537263],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9999138,0.000007946104,0.0000045855736,0.000022985447,0.00003180494,0.000018913319],"domain_scores_gemma":[0.9998627,0.000051320974,0.000035092748,0.0000140734055,0.000015047127,0.00002188536],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.000074081254,0.00017073566,0.00020038856,0.0007160611,0.00020619587,0.0003481393,0.00015850678,0.00023383755,0.0021642868],"category_scores_gemma":[0.00035282673,0.00017062807,0.00015846491,0.00036749916,0.00015555846,0.00007670999,0.00024824313,0.00026044206,0.00035235175],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00038376867,0.000040410832,0.034074213,0.00007980045,0.00006639987,0.0022261012,0.00014842917,0.00077219337,0.94654125,0.00097450765,0.00051485153,0.014178185],"study_design_scores_gemma":[0.000053131673,0.0004028612,0.6975428,0.000033269822,0.00021883681,0.017341517,0.00047904407,0.0048268135,0.26318184,0.0016985225,0.014193702,0.000027567241],"about_ca_topic_score_codex":0.0020263803,"about_ca_topic_score_gemma":0.0040472834,"teacher_disagreement_score":0.0021642868,"about_ca_system_score_codex":0.00020573025,"about_ca_system_score_gemma":0.0001848369,"threshold_uncertainty_score":0.007240236},"labels":[],"label_agreement":null},{"id":"W3013568573","doi":"10.1038/s41588-020-0604-7","title":"Stepwise selection on homeologous PRR genes controlling flowering and maturity during soybean domestication","year":2020,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Soybean genetics and cultivation","field":"Agricultural and Biological Sciences","cited_by":381,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Institute of Genetics","funders":"","keywords":"Domestication; Biology; Germplasm; Crop; Phenology; Dormancy; Adaptation (eye); Gene; Genetics; Botany; Agronomy","score_opus":0.011004315318233484,"score_gpt":0.2165535047550208,"score_spread":0.20554918943678732,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W3013568573","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9993704,0.00003730714,0.0002962872,0.000012031442,0.0000020637995,0.0000041311173,0.000039859708,0.000014991003,0.00022288598],"genre_scores_gemma":[0.99856335,0.000045306908,0.00054398505,0.00004527102,0.0000032603994,0.000010950197,0.00017365711,0.00003688512,0.0005773679],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9997887,0.00005867563,0.000015864698,0.00005214629,0.000034039393,0.00005057895],"domain_scores_gemma":[0.9993161,0.0003519132,0.000113416514,0.000046853882,0.000034531084,0.00013713117],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0003998196,0.0003393086,0.00031021688,0.00049053674,0.00019723974,0.00032981895,0.00041778106,0.00027003032,0.0011166363],"category_scores_gemma":[0.00045182914,0.00027445337,0.0002904628,0.00031973718,0.00031755603,0.00015931715,0.00046685032,0.00074146525,0.00015842535],"study_design_candidate":"bench_or_experimental","study_design_consensus":"bench_or_experimental","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0002752476,0.000025270878,0.0025322929,0.00000982968,0.000010926559,0.000085413834,0.00006155331,0.00008008643,0.9955064,0.00008358016,0.000010198582,0.0013192686],"study_design_scores_gemma":[0.00024823437,0.0014153488,0.47197336,0.000019474395,0.00022624101,0.0016130112,0.00055956567,0.0057645454,0.5157735,0.00035361756,0.0019906391,0.00006252701],"about_ca_topic_score_codex":0.0006529431,"about_ca_topic_score_gemma":0.0026852181,"teacher_disagreement_score":0.0011166363,"about_ca_system_score_codex":0.00038910165,"about_ca_system_score_gemma":0.00024861214,"threshold_uncertainty_score":0.0037354827},"labels":[],"label_agreement":null},{"id":"W3013660197","doi":"10.1038/s41588-020-0594-5","title":"Minimal phenotyping yields genome-wide association signals of low specificity for major depression","year":2020,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Genetic Associations and Epidemiology","field":"Biochemistry, Genetics and Molecular Biology","cited_by":375,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Dalhousie University","funders":"Cilag; National Institute of Mental Health; Neuraxpharm; Chinese Society of Clinical Oncology; University of Oxford; European Bioinformatics Institute; King's College London; National Institute for Health and Care Research; Fresenius Medical Care North America; Schweizerischer Nationalfonds zur Förderung der Wissenschaftlichen Forschung; Wellcome Trust; NIHR Maudsley Biomedical Research Centre; GlaxoSmithKline; John Templeton Foundation; Lundbeckfonden; National Science Foundation","keywords":"Biology; Genome-wide association study; Genetics; Computational biology; Genome; Genetic association; Association (psychology); Evolutionary biology; Gene; Single-nucleotide polymorphism; Genotype","score_opus":0.01340830698091785,"score_gpt":0.26209553183218187,"score_spread":0.24868722485126402,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W3013660197","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9265272,0.000670088,0.06721469,0.00065273675,0.00006610788,0.00010175579,0.0014912437,0.0002648813,0.0030112104],"genre_scores_gemma":[0.9903284,0.00010824525,0.008557056,0.00019003233,0.000019051853,0.00003536371,0.00054710236,0.000032994147,0.00018184027],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99399984,0.0032895296,0.00035671378,0.0014842458,0.000510918,0.00035881155],"domain_scores_gemma":[0.9861195,0.008139458,0.0025235421,0.0023963056,0.0005209934,0.00030018305],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.005246327,0.0006329091,0.0008227504,0.00098525,0.00043546324,0.0011695587,0.00037481205,0.0005824124,0.0016510702],"category_scores_gemma":[0.016994053,0.00032645042,0.0007173595,0.00097065174,0.001009209,0.00045611628,0.0013226558,0.0007445042,0.00037557373],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0011256976,0.00009703533,0.877923,0.00025130864,0.0009327031,0.0008788204,0.000480901,0.0028689306,0.06786741,0.004730958,0.0017146555,0.041128527],"study_design_scores_gemma":[0.000060483002,0.00034492835,0.95387274,0.00006990897,0.00037530027,0.0022086482,0.00016682238,0.007900069,0.013904956,0.017413408,0.003648439,0.000034370634],"about_ca_topic_score_codex":0.0009715955,"about_ca_topic_score_gemma":0.0017441772,"teacher_disagreement_score":0.005246327,"about_ca_system_score_codex":0.0002539338,"about_ca_system_score_gemma":0.00034958104,"threshold_uncertainty_score":0.027745545},"labels":[],"label_agreement":null},{"id":"W3018522922","doi":"10.1038/s41588-020-0611-8","title":"Genome-wide association meta-analyses combining multiple risk phenotypes provide insights into the genetic architecture of cutaneous melanoma susceptibility","year":2020,"lang":"en","type":"review","venue":"Nature Genetics","topic":"Genetic Associations and Epidemiology","field":"Biochemistry, Genetics and Molecular Biology","cited_by":239,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"McGill University and Génome Québec Innovation Centre","funders":"National Cancer Institute; Medical Research Council; National Institutes of Health; Cancer Research UK; Wellcome Trust","keywords":"Genome-wide association study; Genetic architecture; Biology; Melanoma; Genetics; Genetic association; Single-nucleotide polymorphism; Meta-analysis; Genetic predisposition; Phenotype; Genotype; Gene; Medicine; Pathology","score_opus":0.03320246374491177,"score_gpt":0.3182490722568541,"score_spread":0.28504660851194236,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W3018522922","genre_codex":"review","genre_gemma":"review","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"review","genre_consensus":"review","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.00013844339,0.99840754,0.0003492313,0.00062910595,0.00016618261,0.0000033711483,0.000091440765,0.000009997817,0.0002047628],"genre_scores_gemma":[0.0017309401,0.9964228,0.0005225556,0.0005829165,0.0004093944,0.000011173721,0.00014776563,0.000004798179,0.00016755078],"study_design_codex":"design_other","study_design_gemma":"meta_analysis","domain_scores_codex":[0.9991911,0.00030338805,0.00010669146,0.00018066836,0.00017373562,0.00004430045],"domain_scores_gemma":[0.99546623,0.003593997,0.00031846043,0.00012809872,0.00037740901,0.000115760326],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0035300408,0.0014757653,0.0037956093,0.002022114,0.00015514177,0.001364434,0.0015998656,0.0015928,0.0032094305],"category_scores_gemma":[0.005899592,0.0005064602,0.0024022348,0.0029877876,0.0004232345,0.0008614767,0.001005082,0.0024364893,0.0008717394],"study_design_candidate":"meta_analysis","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0006084896,0.00004027849,0.0029464874,0.031479154,0.009521524,0.00023934427,0.000037774535,0.0007196946,0.000751931,0.0036432198,0.029755164,0.920257],"study_design_scores_gemma":[0.0008643108,0.00044846348,0.036408037,0.04550078,0.04771193,0.0036122345,0.00018584111,0.0012764101,0.0010996896,0.03446161,0.8281668,0.00026394814],"about_ca_topic_score_codex":0.0021359255,"about_ca_topic_score_gemma":0.0049985833,"teacher_disagreement_score":0.0037956093,"about_ca_system_score_codex":0.0006952103,"about_ca_system_score_gemma":0.0017394985,"threshold_uncertainty_score":0.01866889},"labels":[],"label_agreement":null},{"id":"W3019747475","doi":"10.1038/s41588-020-0610-9","title":"Genetic identification of cell types underlying brain complex traits yields insights into the etiology of Parkinson’s disease","year":2020,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Genetic Associations and Epidemiology","field":"Biochemistry, Genetics and Molecular Biology","cited_by":387,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Toronto General Hospital; Hospital for Sick Children; Centre for Addiction and Mental Health; University of Toronto","funders":"National Institute of Mental Health; Perelman School of Medicine, University of Pennsylvania; UK Dementia Research Institute; National Center of Neurology and Psychiatry; Broad Institute; Uniwersytet Medyczny im. Karola Marcinkowskiego w Poznaniu; Universität Duisburg-Essen; Rheinische Friedrich-Wilhelms-Universität Bonn; Medical Research Council; Tartu Ülikool; RWTH Aachen University; Centre National de la Recherche Scientifique; Universitat de Barcelona; Göteborgs Universitet; Cancerfonden; Université Paris Descartes; Universitetet i Oslo; National Institute of General Medical Sciences; National and Kapodistrian University of Athens; Karolinska Institutet; Lundbeckfonden; Hjärnfonden; Università degli Studi di Padova; Université de Montpellier; University of Pennsylvania; Technische Universität Dresden; Medizinischen Hochschule Hannover; University of Toronto; Schweizerischer Nationalfonds zur Förderung der Wissenschaftlichen Forschung; Sahlgrenska Akademin; H. Lundbeck A/S; University of Bristol; Bundesministerium für Bildung und Forschung; Pfizer; Institut National de la Santé et de la Recherche Médicale; Universitat Pompeu Fabra; Agence Nationale de la Recherche; Kommunfullmäktige, Stockholms Stad; Alzheimer's Society; Wellcome Trust; Universität Basel; Massachusetts Institute of Technology; European Commission; University of Otago; QIMR Berghofer Medical Research Institute; Aarhus Universitet; Harokopio University; National Science Foundation; University of Minnesota; Vetenskapsrådet; Virginia Commonwealth University; Harvard University; Stiftelsen för Strategisk Forskning; Michael J. Fox Foundation for Parkinson's Research","keywords":"Biology; Parkinson's disease; Identification (biology); Disease; Genetics; Complex disease; Etiology; Computational biology; Cell type; Neuroscience; Cell; Bioinformatics; Gene; Internal medicine","score_opus":0.024637225550198354,"score_gpt":0.2832840162601184,"score_spread":0.25864679070992,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W3019747475","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.98863214,0.0017109655,0.005762791,0.00050873816,0.000037376085,0.00001702841,0.0015529774,0.000043542328,0.0017344174],"genre_scores_gemma":[0.99649185,0.00096806727,0.0016089372,0.00008471855,0.00003808839,0.000012448931,0.00039360436,0.00001674412,0.00038545355],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9993845,0.00014376649,0.000052624142,0.00019330236,0.00016828984,0.000057424575],"domain_scores_gemma":[0.9983475,0.00064522045,0.00060557824,0.0001486393,0.00015968582,0.00009334917],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0005032188,0.0005624922,0.00053040485,0.0024471472,0.00039168427,0.0010042225,0.0004923578,0.00079650903,0.00215138],"category_scores_gemma":[0.0025897447,0.00028832373,0.000378256,0.0015182009,0.0008588797,0.00051622133,0.0006804681,0.0007638977,0.00028667392],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0011447879,0.00008395997,0.7658785,0.00011142826,0.00050744216,0.002187103,0.00045879837,0.0008588616,0.1978113,0.0041917395,0.00085738854,0.025908701],"study_design_scores_gemma":[0.00003530648,0.00012965327,0.9535297,0.000034102733,0.000233741,0.0047970517,0.00035950565,0.0020862892,0.029003805,0.007231497,0.0025233557,0.000035940742],"about_ca_topic_score_codex":0.0025940938,"about_ca_topic_score_gemma":0.0016581077,"teacher_disagreement_score":0.0025940938,"about_ca_system_score_codex":0.00037913487,"about_ca_system_score_gemma":0.00025587977,"threshold_uncertainty_score":0.0071970224},"labels":[],"label_agreement":null},{"id":"W3024294833","doi":"10.1038/s41588-020-0609-2","title":"Genome-wide association study identifies 32 novel breast cancer susceptibility loci from overall and subtype-specific analyses","year":2020,"lang":"en","type":"review","venue":"Nature Genetics","topic":"Genetic Associations and Epidemiology","field":"Biochemistry, Genetics and Molecular Biology","cited_by":567,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of British Columbia; Université Laval; Centre hospitalier universitaire de Québec; University of Toronto; University Health Network; Royal Victoria Hospital; McGill University; Queen's University; Centre hospitalier de l'Université Laval; Lunenfeld-Tanenbaum Research Institute; Mount Sinai Hospital","funders":"National Institute of Environmental Health Sciences; National Institute of General Medical Sciences; National Cancer Institute; National Center for Advancing Translational Sciences; National Human Genome Research Institute; National Heart, Lung, and Blood Institute; Medical Research Council; Deutsche Krebshilfe; Canadian Institutes of Health Research; Associazione Italiana per la Ricerca sul Cancro; Genome Canada; Odense Universitetshospital; Fondation du cancer du sein du Québec; National Institutes of Health; U.S. Department of Health and Human Services; Ovarian Cancer Research Fund; European Commission; Breast Cancer Research Foundation; Génome Québec; National Health and Medical Research Council; Cancer Research UK; Government of Canada","keywords":"Biology; Genome-wide association study; Genetics; Breast cancer; Computational biology; Genetic association; Genome; Cancer; Single-nucleotide polymorphism; Gene; Genotype","score_opus":0.03999402770371705,"score_gpt":0.34873610373327363,"score_spread":0.30874207602955656,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W3024294833","genre_codex":"review","genre_gemma":"review","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"review","genre_consensus":"review","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.00016866405,0.9975667,0.00036078697,0.0008521631,0.0002442138,0.000004966932,0.00011712199,0.000016810223,0.00066863967],"genre_scores_gemma":[0.0009444983,0.99640733,0.0005866299,0.0008843907,0.00035724338,0.000011468197,0.0002199707,0.0000044715866,0.0005839874],"study_design_codex":"design_other","study_design_gemma":"observational","domain_scores_codex":[0.99964774,0.00007155887,0.000045082143,0.00009260353,0.000112082984,0.000030957417],"domain_scores_gemma":[0.9988293,0.0006943127,0.000100358404,0.000037959067,0.00025000382,0.00008804369],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0017493446,0.0011953077,0.0020411955,0.0017584146,0.0001823461,0.0010497401,0.001287799,0.0012416005,0.002932349],"category_scores_gemma":[0.0018248137,0.0003300473,0.00074951496,0.002324205,0.00045848658,0.0007096021,0.00084235135,0.0020351037,0.001973931],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00021453739,0.000041794698,0.0013568786,0.0064854505,0.00047701626,0.00023903538,0.000023672359,0.00018086079,0.0010173013,0.0019092264,0.04549957,0.94255465],"study_design_scores_gemma":[0.00016023222,0.0001403289,0.010199361,0.005519099,0.0015263417,0.0019295964,0.00006986962,0.00014116541,0.0006162125,0.004925325,0.97470266,0.00006975471],"about_ca_topic_score_codex":0.002144459,"about_ca_topic_score_gemma":0.005235508,"teacher_disagreement_score":0.002932349,"about_ca_system_score_codex":0.0006543978,"about_ca_system_score_gemma":0.0016030677,"threshold_uncertainty_score":0.009809673},"labels":[],"label_agreement":null},{"id":"W3024406068","doi":"10.1038/s41588-020-0634-1","title":"Publisher Correction: Comprehensive analysis of chromothripsis in 2,658 human cancers using whole-genome sequencing","year":2020,"lang":"en","type":"erratum","venue":"Nature Genetics","topic":"Cancer Genomics and Diagnostics","field":"Biochemistry, Genetics and Molecular Biology","cited_by":13,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Ottawa; University of Toronto; Ontario Institute for Cancer Research","funders":"National Cancer Institute","keywords":"Chromothripsis; Biology; Computational biology; Genetics; Genome; Human genome; DNA sequencing; DNA; Gene; Genome instability","score_opus":0.01917632796000852,"score_gpt":0.28142329271083255,"score_spread":0.26224696475082404,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W3024406068","genre_codex":"editorial","genre_gemma":"editorial","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"editorial","genre_consensus":"editorial","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.00019624094,0.00069226115,0.00094505894,0.023213306,0.966783,0.000023064193,0.0026013635,0.0006637726,0.004881833],"genre_scores_gemma":[0.015403984,0.0069136187,0.0123919705,0.073395915,0.30360758,0.00034459427,0.012121087,0.005529179,0.5702921],"study_design_codex":"not_applicable","study_design_gemma":"not_applicable","domain_scores_codex":[0.9966691,0.00037999102,0.0004692943,0.00045035948,0.0017475719,0.00028359494],"domain_scores_gemma":[0.9734441,0.005401605,0.00097640563,0.0022464914,0.01644116,0.001490277],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0036171747,0.0020402651,0.0018886549,0.004546185,0.003432591,0.0042129587,0.0040045986,0.0051121647,0.08755835],"category_scores_gemma":[0.038224667,0.0013311026,0.0015331877,0.002832341,0.0017141486,0.001895301,0.0018138654,0.009399243,0.04284988],"study_design_candidate":"not_applicable","study_design_consensus":"not_applicable","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.000017221699,0.0000036709027,0.00004702252,0.0000618304,0.000008844578,0.00016110245,0.000010981523,0.000029776695,0.00004651251,0.00032270688,0.9951983,0.004092004],"study_design_scores_gemma":[0.00003838929,0.000012589925,0.0008373493,0.00020088993,0.00004912116,0.0005607553,0.000039017454,0.00018480269,0.0004394142,0.0010895315,0.99651587,0.000032211465],"about_ca_topic_score_codex":0.022513187,"about_ca_topic_score_gemma":0.034692228,"teacher_disagreement_score":0.08755835,"about_ca_system_score_codex":0.0037082783,"about_ca_system_score_gemma":0.0057242108,"threshold_uncertainty_score":0.2929119},"labels":[],"label_agreement":null},{"id":"W3034530539","doi":"10.1038/s41588-020-0658-6","title":"Author Correction: A transcriptomic analysis of the phylum Nematoda","year":2020,"lang":"en","type":"erratum","venue":"Nature Genetics","topic":"Nematode management and characterization studies","field":"Agricultural and Biological Sciences","cited_by":0,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"SickKids Foundation; Hospital for Sick Children; University of Toronto","funders":"","keywords":"Biology; Phylum; Transcriptome; Computational biology; Evolutionary biology; Genetics; Gene; Gene expression","score_opus":0.015616673368891233,"score_gpt":0.2373355904553908,"score_spread":0.22171891708649957,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W3034530539","genre_codex":"editorial","genre_gemma":"other","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"other","genre_consensus":null,"domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.00029416755,0.00048078469,0.0012447995,0.03536949,0.95695704,0.000020729243,0.0016664042,0.00051676703,0.0034499273],"genre_scores_gemma":[0.026450293,0.006170522,0.0149819255,0.096726686,0.33648556,0.00029226657,0.007838597,0.0052035144,0.5058506],"study_design_codex":"not_applicable","study_design_gemma":"not_applicable","domain_scores_codex":[0.9960271,0.00042759377,0.00047809837,0.0006282135,0.0021738335,0.00026511645],"domain_scores_gemma":[0.96369696,0.0062459675,0.0013380958,0.0021869682,0.024767349,0.0017646188],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0033716096,0.0015632295,0.0011355462,0.0033020582,0.0034291202,0.0031394719,0.002602866,0.0042228363,0.055708587],"category_scores_gemma":[0.040337548,0.0007963258,0.0010653,0.0018702282,0.0019979132,0.0019186081,0.002027064,0.00758886,0.032130312],"study_design_candidate":"not_applicable","study_design_consensus":"not_applicable","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.000028030583,0.0000050309673,0.000081032944,0.000081728256,0.0000081171975,0.00022475324,0.000023849467,0.00003316869,0.00017850804,0.0005400085,0.99441344,0.004382353],"study_design_scores_gemma":[0.00002961642,0.000013008137,0.00083886227,0.0001699691,0.000036909867,0.000628008,0.000071766844,0.00023384152,0.0010916735,0.0012764514,0.99557686,0.000032996963],"about_ca_topic_score_codex":0.016316745,"about_ca_topic_score_gemma":0.021106351,"teacher_disagreement_score":0.055708587,"about_ca_system_score_codex":0.0032960281,"about_ca_system_score_gemma":0.005475558,"threshold_uncertainty_score":0.18636382},"labels":[],"label_agreement":null},{"id":"W3037588075","doi":"10.1038/s41588-020-0653-y","title":"High-definition likelihood inference of genetic correlations across human complex traits","year":2020,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Genetic Associations and Epidemiology","field":"Biochemistry, Genetics and Molecular Biology","cited_by":294,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Centre for Global Health Research","funders":"Medical Research Council; Vetenskapsrådet","keywords":"Genetic correlation; Biology; Genome-wide association study; Linkage disequilibrium; Biobank; Genetic architecture; Correlation; Genetic association; Statistics; Heritability; Inference; Regression; Genetics; Genetic variation; Computational biology; Quantitative trait locus; Single-nucleotide polymorphism; Computer science; Mathematics; Gene; Artificial intelligence; Genotype","score_opus":0.03166090575327395,"score_gpt":0.3096036471214217,"score_spread":0.2779427413681477,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W3037588075","genre_codex":"methods","genre_gemma":"methods","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"methods","genre_consensus":"methods","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.099083714,0.00092928944,0.89631075,0.00097378663,0.00005025507,0.00005952794,0.00072186295,0.00078407384,0.0010867878],"genre_scores_gemma":[0.8179888,0.00043503,0.17510615,0.00065526174,0.00017177127,0.00016894443,0.002984294,0.00030137828,0.0021883885],"study_design_codex":"simulation_or_modeling","study_design_gemma":"theoretical_or_conceptual","domain_scores_codex":[0.99055475,0.006601251,0.00035197788,0.0016387268,0.0005521517,0.00030106938],"domain_scores_gemma":[0.8858949,0.10445661,0.002304733,0.0054321974,0.00092398055,0.0009875671],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.016720101,0.00088692055,0.0023618967,0.0019831953,0.0015189968,0.003676379,0.00426359,0.0023048916,0.0027463564],"category_scores_gemma":[0.07946754,0.0019964029,0.001887343,0.0019262552,0.0025251075,0.0029755149,0.004266279,0.005081411,0.0007667738],"study_design_candidate":"theoretical_or_conceptual","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0020384467,0.0005666814,0.20417364,0.0009906223,0.0028013305,0.0028503991,0.0015010852,0.41498467,0.009994176,0.18397194,0.00999669,0.16613029],"study_design_scores_gemma":[0.0002339855,0.0000954062,0.016061837,0.00007735865,0.00020961126,0.0008713504,0.00011451615,0.7779116,0.0016373867,0.20086825,0.0018519445,0.000066862325],"about_ca_topic_score_codex":0.002464126,"about_ca_topic_score_gemma":0.004444367,"teacher_disagreement_score":0.016720101,"about_ca_system_score_codex":0.0007787911,"about_ca_system_score_gemma":0.0013426251,"threshold_uncertainty_score":0.0884254},"labels":[],"label_agreement":null},{"id":"W3041912701","doi":"10.1038/s41588-020-0648-8","title":"The DNA methylation landscape of advanced prostate cancer","year":2020,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Epigenetics and DNA Methylation","field":"Biochemistry, Genetics and Molecular Biology","cited_by":353,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of British Columbia; Princess Margaret Cancer Centre; BC Cancer Agency; University Health Network; University of Toronto; Ontario Institute for Cancer Research","funders":"Janssen Biotech; National Cancer Institute; National Institute of Environmental Health Sciences; Astellas Pharma; Howard Hughes Medical Institute","keywords":"Biology; DNA methylation; Epigenomics; Transcriptome; Epigenetics; Bisulfite sequencing; Methylation; Prostate cancer; Illumina Methylation Assay; Genetics; DNMT3B; Gene; Genome; Cancer research; Cancer; Gene expression","score_opus":0.007079124434383316,"score_gpt":0.2722507145645297,"score_spread":0.2651715901301464,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W3041912701","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.98078096,0.011108939,0.0022184425,0.0011398114,0.00001908841,0.000008512443,0.00068703206,0.00006761417,0.0039695986],"genre_scores_gemma":[0.9967595,0.0019170649,0.00022463087,0.00008270465,0.000016155323,0.0000024013868,0.00013778188,0.0000066773864,0.0008531301],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.99990845,0.000017674272,0.0000031830155,0.00001940806,0.000030849125,0.00002039201],"domain_scores_gemma":[0.9999454,0.000011070279,0.00001357789,0.0000040145237,0.000011338035,0.0000145991735],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00013584591,0.000101610545,0.00019376627,0.00047676847,0.00013274654,0.0004233277,0.00016226567,0.0001656466,0.0011131676],"category_scores_gemma":[0.00025806867,0.000145312,0.00008143603,0.00047180292,0.00020708583,0.00016326313,0.00022741905,0.0002909803,0.00013833743],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0007123984,0.000042440843,0.14530782,0.00022183207,0.00017645898,0.00068986835,0.0004947258,0.0033252703,0.7570252,0.0055230386,0.0016693162,0.08481168],"study_design_scores_gemma":[0.000023832828,0.0003114985,0.8855934,0.000029342793,0.00012852243,0.0030186677,0.00058929436,0.005275934,0.074570596,0.008878017,0.021540584,0.000040322262],"about_ca_topic_score_codex":0.0026145244,"about_ca_topic_score_gemma":0.0033931744,"teacher_disagreement_score":0.0026145244,"about_ca_system_score_codex":0.00029759508,"about_ca_system_score_gemma":0.00024146726,"threshold_uncertainty_score":0.0051985383},"labels":[],"label_agreement":null},{"id":"W3046437178","doi":"10.1038/s41588-020-0673-7","title":"Analysis of Ugandan cervical carcinomas identifies human papillomavirus clade–specific epigenome and transcriptome landscapes","year":2020,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Cervical Cancer and HPV Research","field":"Medicine","cited_by":78,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of British Columbia; Canada's Michael Smith Genome Sciences Centre","funders":"National Institute of Allergy and Infectious Diseases; U.S. Department of Health and Human Services; National Cancer Institute; National Institutes of Health; Canadian Institutes of Health Research; Canada's Michael Smith Genome Sciences Centre","keywords":"Biology; Epigenome; DNA methylation; Histone; Transcriptome; Cervical cancer; Gene; Genetics; Genome; Population; Epigenetics; Gene expression profiling; Methylation; Epigenomics; Cancer research; Cancer; Gene expression; Medicine","score_opus":0.032881767652732506,"score_gpt":0.3219029235151969,"score_spread":0.2890211558624644,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W3046437178","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99845624,0.00049531035,0.000317361,0.000011672126,8.751089e-7,0.000007490191,0.00046940014,0.0000059820923,0.00023564664],"genre_scores_gemma":[0.99769443,0.0003927383,0.00097220764,0.000015362186,0.0000011258671,0.00001704456,0.00068694487,0.000004593636,0.00021558994],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.999931,0.000013036054,0.0000037800708,0.000023180508,0.000011894526,0.000017034516],"domain_scores_gemma":[0.99991536,0.000021857397,0.000027595235,0.000013947279,0.0000121466,0.000009055868],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00009946154,0.00010802505,0.00014925945,0.00049609365,0.00025236545,0.00026257432,0.00007745504,0.000115790644,0.0007018483],"category_scores_gemma":[0.0002329961,0.00013047647,0.000109029184,0.0004649621,0.00014910568,0.00008282728,0.00036066998,0.00013753497,0.00011707911],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0005992615,0.00003569863,0.2802894,0.00021748994,0.0000935128,0.0003709103,0.0010628164,0.00048324876,0.6886253,0.00016445725,0.00022664774,0.027831333],"study_design_scores_gemma":[0.000008463258,0.00013035652,0.95886713,0.00002387273,0.00004344134,0.001646785,0.0005069833,0.0006350332,0.035577968,0.00015827296,0.002394557,0.0000071151785],"about_ca_topic_score_codex":0.000832739,"about_ca_topic_score_gemma":0.0018147705,"teacher_disagreement_score":0.000832739,"about_ca_system_score_codex":0.00012542048,"about_ca_system_score_gemma":0.00009784473,"threshold_uncertainty_score":0.0023478866},"labels":[],"label_agreement":null},{"id":"W3082264507","doi":"10.1038/s41588-020-0681-7","title":"Chromatin binding of FOXA1 is promoted by LSD1-mediated demethylation in prostate cancer","year":2020,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Prostate Cancer Treatment and Research","field":"Medicine","cited_by":124,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Princess Margaret Cancer Centre; University of Toronto; University Health Network","funders":"National Institute of General Medical Sciences; Canadian Institutes of Health Research; Terry Fox Foundation; Prostate Cancer Canada; Congressionally Directed Medical Research Programs; Princess Margaret Cancer Foundation; National Cancer Institute; U.S. Department of Health and Human Services; National Institute of Diabetes and Digestive and Kidney Diseases; U.S. Department of Defense","keywords":"FOXA1; Biology; Chromatin; Demethylation; Prostate cancer; Cancer; Cancer research; Genetics; DNA methylation; DNA; Breast cancer; Gene; Gene expression","score_opus":0.02013716219593562,"score_gpt":0.33092180122396075,"score_spread":0.3107846390280251,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W3082264507","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.98840374,0.005641763,0.0017736807,0.0003849249,0.000076145465,0.000012391772,0.0005157122,0.00014737538,0.0030443158],"genre_scores_gemma":[0.99696535,0.00034255793,0.00023223371,0.000051467432,0.000007741286,0.000004645646,0.00023820621,0.000010526239,0.0021473097],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9998418,0.000021565591,0.0000065709273,0.00003664466,0.0000372663,0.000056059027],"domain_scores_gemma":[0.9998847,0.000011475255,0.000034598514,0.0000112831785,0.000015204506,0.000042690674],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00021117965,0.00015616987,0.00019188852,0.00035369172,0.0003850363,0.00040265676,0.00023494243,0.00019500269,0.0034166132],"category_scores_gemma":[0.0001671254,0.00024333701,0.00034419628,0.00016124816,0.00029311786,0.00015971855,0.00033628626,0.0004075397,0.00044157484],"study_design_candidate":"bench_or_experimental","study_design_consensus":"bench_or_experimental","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0006845443,0.00005160994,0.011120718,0.00008346896,0.000060562623,0.00018895332,0.00007725494,0.00020477717,0.9818855,0.00061494467,0.00068094564,0.0043468573],"study_design_scores_gemma":[0.00006997184,0.0004517978,0.30835715,0.000019447682,0.0000842991,0.0012217752,0.00036825304,0.0018604652,0.67413574,0.0005633009,0.012840066,0.00002769157],"about_ca_topic_score_codex":0.0021583377,"about_ca_topic_score_gemma":0.004505697,"teacher_disagreement_score":0.0034166132,"about_ca_system_score_codex":0.0005716981,"about_ca_system_score_gemma":0.00037796225,"threshold_uncertainty_score":0.011429787},"labels":[],"label_agreement":null},{"id":"W3084552931","doi":"10.1038/s41588-020-0689-z","title":"NSD1-deposited H3K36me2 directs de novo methylation in the mouse male germline and counteracts Polycomb-associated silencing","year":2020,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Epigenetics and DNA Methylation","field":"Biochemistry, Genetics and Molecular Biology","cited_by":156,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of British Columbia","funders":"Canadian Institutes of Health Research; Government of Canada; Japan Agency for Medical Research and Development","keywords":"Biology; Gene silencing; Germline; Polycomb-group proteins; Methylation; Genetics; Cell biology; Gene; Repressor; Transcription factor","score_opus":0.009439743877810432,"score_gpt":0.26109782869137493,"score_spread":0.2516580848135645,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W3084552931","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9886304,0.0016350707,0.0050174715,0.0002625683,0.0001007369,0.000017865987,0.0005850152,0.0003508945,0.003399851],"genre_scores_gemma":[0.9906151,0.00040373227,0.0010822059,0.0000670352,0.000008452481,0.000010005342,0.00028974024,0.00007546133,0.007448224],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99968266,0.000024140369,0.000022045973,0.00009881969,0.00010850892,0.00006383035],"domain_scores_gemma":[0.9997359,0.000022692053,0.000083510815,0.000039680213,0.000019687917,0.000098555305],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00023625945,0.0003108896,0.00027385246,0.00047011132,0.00027524974,0.00055069797,0.00053365773,0.00036253806,0.0025049436],"category_scores_gemma":[0.00015251174,0.0003680405,0.00023719703,0.00017579134,0.00061313197,0.00020194123,0.0004552111,0.00072157517,0.00056077144],"study_design_candidate":"bench_or_experimental","study_design_consensus":"bench_or_experimental","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00005688986,0.0000057664656,0.00017177858,0.00001378227,0.000004411775,0.000023661478,0.000008564766,0.000037353748,0.9988341,0.00020598198,0.000029492237,0.0006082473],"study_design_scores_gemma":[0.000012378213,0.000053453925,0.003930758,0.0000035340772,0.000008875176,0.00008356964,0.000026042591,0.0004134538,0.99382544,0.00007593016,0.0015632359,0.0000033586382],"about_ca_topic_score_codex":0.0016021354,"about_ca_topic_score_gemma":0.0046505276,"teacher_disagreement_score":0.0025049436,"about_ca_system_score_codex":0.00063722464,"about_ca_system_score_gemma":0.00038006855,"threshold_uncertainty_score":0.008379877},"labels":[],"label_agreement":null},{"id":"W3090167646","doi":"10.1038/s41588-020-0695-1","title":"Mutations disrupting neuritogenesis genes confer risk for cerebral palsy","year":2020,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Cerebral Palsy and Movement Disorders","field":"Medicine","cited_by":175,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Centre for Addiction and Mental Health","funders":"Eunice Kennedy Shriver National Institute of Child Health and Human Development; National Heart, Lung, and Blood Institute; Doris Duke Charitable Foundation; National Institute of Neurological Disorders and Stroke; National Human Genome Research Institute; U.S. Department of Health and Human Services","keywords":"Biology; Exome sequencing; RHOB; Genetics; Mutation; Exome; Gene","score_opus":0.022253780904628,"score_gpt":0.2971123776396101,"score_spread":0.27485859673498214,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W3090167646","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.98736495,0.0011135574,0.0026074497,0.0008807922,0.00018616626,0.000035752924,0.00092885527,0.00013723741,0.006745178],"genre_scores_gemma":[0.9958697,0.0003398351,0.0014641789,0.00016474102,0.0000943364,0.000013097518,0.00032314024,0.000069604626,0.0016613345],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.99916065,0.00020875891,0.00010220338,0.00018112623,0.00022701772,0.000120307704],"domain_scores_gemma":[0.9984478,0.00070138206,0.0004663135,0.000071331335,0.00007624354,0.00023679648],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.000344398,0.0012699323,0.0005361519,0.0023878147,0.00095630763,0.0005776627,0.0009569584,0.0023137894,0.012223552],"category_scores_gemma":[0.0020921691,0.0005072167,0.0008444826,0.0010362417,0.00084198295,0.00034287726,0.0009185966,0.001010491,0.0007202046],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0045024557,0.000839124,0.37126037,0.00032416766,0.0016540019,0.08818603,0.001401156,0.0038780759,0.48060063,0.0058813696,0.003920866,0.03755171],"study_design_scores_gemma":[0.00034526116,0.0010300204,0.7909581,0.0002819117,0.0015969487,0.11820913,0.0007344059,0.0041284263,0.06605529,0.004460431,0.012029688,0.0001704378],"about_ca_topic_score_codex":0.0038541425,"about_ca_topic_score_gemma":0.0034575139,"teacher_disagreement_score":0.012223552,"about_ca_system_score_codex":0.00037475541,"about_ca_system_score_gemma":0.00039661847,"threshold_uncertainty_score":0.040891826},"labels":[],"label_agreement":null},{"id":"W3091076281","doi":"10.1038/s41588-020-0708-0","title":"Somatic mutation distributions in cancer genomes vary with three-dimensional chromatin structure","year":2020,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Cancer Genomics and Diagnostics","field":"Biochemistry, Genetics and Molecular Biology","cited_by":124,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Ottawa","funders":"National Cancer Institute; National Eye Institute; National Institutes of Health; Welch Foundation","keywords":"Biology; Genetics; Somatic cell; Chromatin; Genome; Mutation; Cancer; Computational biology; DNA; Gene","score_opus":0.0059876561741675095,"score_gpt":0.24022901153712423,"score_spread":0.2342413553629567,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W3091076281","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99630827,0.00027330712,0.0024438072,0.000041223633,0.0000032088758,0.0000027229014,0.00020851682,0.00006286861,0.00065594923],"genre_scores_gemma":[0.99895906,0.00005673535,0.00046591912,0.000023684826,0.000002418065,0.0000035795215,0.00020059563,0.000023319517,0.00026468956],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9997689,0.000037724596,0.000016245802,0.0000743947,0.00006441433,0.000038378508],"domain_scores_gemma":[0.99874324,0.0005927834,0.00028414448,0.00012647976,0.00013338824,0.000119988],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0002924443,0.00009329412,0.00020238594,0.000841865,0.0002159031,0.0006516187,0.00021482033,0.00031257735,0.0019273805],"category_scores_gemma":[0.0012068248,0.00026468188,0.0002570481,0.0004046529,0.00040219087,0.00039466703,0.00045361274,0.00035639395,0.00039881768],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00041096855,0.0000346695,0.10538818,0.000044908054,0.00012142578,0.00010425852,0.00016491211,0.0020591686,0.88084507,0.0009681937,0.00015190865,0.009706377],"study_design_scores_gemma":[0.000019018817,0.000120998295,0.8613926,0.000006206202,0.00006389889,0.0006578221,0.00016993468,0.008714694,0.12650748,0.0014258389,0.0008902081,0.000031382337],"about_ca_topic_score_codex":0.0005261209,"about_ca_topic_score_gemma":0.001097067,"teacher_disagreement_score":0.0019273805,"about_ca_system_score_codex":0.00026691396,"about_ca_system_score_gemma":0.000096102776,"threshold_uncertainty_score":0.0064477324},"labels":[],"label_agreement":null},{"id":"W3093094957","doi":"10.1038/s41588-020-00731-9","title":"Interferons and viruses induce a novel truncated ACE2 isoform and not the full-length SARS-CoV-2 receptor","year":2020,"lang":"en","type":"article","venue":"Nature Genetics","topic":"SARS-CoV-2 and COVID-19 Research","field":"Medicine","cited_by":269,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Alberta","funders":"Division of Cancer Epidemiology and Genetics, National Cancer Institute; Kent State University; Deutsche Forschungsgemeinschaft; National Institute on Aging; National Cancer Institute; National Institutes of Health; U.S. Department of Health and Human Services","keywords":"Biology; Gene isoform; Interferon; Virology; TMPRSS2; Coronavirus; Interferon type I; Interferon-stimulated gene; Virus; Receptor; Gene; Coronavirus disease 2019 (COVID-19); Genetics; Innate immune system; Infectious disease (medical specialty); Disease","score_opus":0.07269509757517975,"score_gpt":0.3547558427819187,"score_spread":0.28206074520673896,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W3093094957","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9956317,0.00046599668,0.0013627566,0.00013453946,0.00009873587,0.000017952028,0.00044405542,0.000036150763,0.0018080436],"genre_scores_gemma":[0.9920033,0.00024508426,0.0015855544,0.00014726016,0.000038702,0.000020580665,0.0013707671,0.000033914563,0.0045548924],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9998425,0.000022111852,0.000015635585,0.000031707037,0.000036366724,0.00005168054],"domain_scores_gemma":[0.99974984,0.000051255807,0.000056187884,0.00004180506,0.000025928748,0.00007495008],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00020660598,0.00037071266,0.00022639746,0.00015176392,0.00022248295,0.0004638293,0.00018016402,0.00027017918,0.0024107182],"category_scores_gemma":[0.00017801159,0.00020307387,0.00055169617,0.00007023906,0.0002708146,0.00026499902,0.00016078311,0.0007683848,0.0007752008],"study_design_candidate":"bench_or_experimental","study_design_consensus":"bench_or_experimental","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00017292037,0.000015996264,0.00014153165,0.00000767247,0.0000048800734,0.00009440168,0.000005767047,0.00002444735,0.9991443,0.00011011715,0.000036131598,0.00024174574],"study_design_scores_gemma":[0.00010870299,0.00047549704,0.015884629,0.000007127729,0.000028430088,0.0030281672,0.00009287685,0.0015602103,0.9744632,0.0002284595,0.0041111223,0.000011469815],"about_ca_topic_score_codex":0.0003552504,"about_ca_topic_score_gemma":0.00063586235,"teacher_disagreement_score":0.0024107182,"about_ca_system_score_codex":0.0003797549,"about_ca_system_score_gemma":0.0002594616,"threshold_uncertainty_score":0.008064628},"labels":[],"label_agreement":null},{"id":"W3093879470","doi":"10.1038/s41588-020-00722-w","title":"Triticum population sequencing provides insights into wheat adaptation","year":2020,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Wheat and Barley Genetics and Pathology","field":"Agricultural and Biological Sciences","cited_by":410,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Institute of Genetics","funders":"Biotechnology and Biological Sciences Research Council; China Postdoctoral Science Foundation; National Natural Science Foundation of China","keywords":"Biology; Subspecies; Adaptation (eye); Introgression; Aegilops; Genetic diversity; Convergent evolution; Genome; Selection (genetic algorithm); Population; Evolutionary biology; Ploidy; Genetics; Gene; Phylogenetics; Ecology","score_opus":0.028654020412471726,"score_gpt":0.2372008332860571,"score_spread":0.20854681287358537,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W3093879470","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.94087666,0.0019051469,0.04057952,0.000621638,0.00018030962,0.00009741374,0.0046256543,0.0005432431,0.010570461],"genre_scores_gemma":[0.95911044,0.0015963212,0.023516787,0.00089021114,0.00006558859,0.00011006892,0.00874053,0.00024869147,0.005721262],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9997081,0.000047191705,0.000022284257,0.00013615892,0.000048064503,0.000038231992],"domain_scores_gemma":[0.9996879,0.00011108875,0.000054751,0.0000561671,0.00004374632,0.00004645208],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0007850986,0.00046003942,0.00041687247,0.00082280685,0.00042348533,0.0006769165,0.00041737308,0.0007012856,0.0027126211],"category_scores_gemma":[0.0007035499,0.0003313838,0.00056548073,0.0008706826,0.00021668305,0.0004629459,0.0006612458,0.0014020636,0.0006087973],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00021223933,0.000072106195,0.013224123,0.00012731197,0.00017106035,0.0003116594,0.000497888,0.0008717735,0.94233483,0.0027565411,0.00088175153,0.03853868],"study_design_scores_gemma":[0.00033607284,0.00068635825,0.7103555,0.0001869778,0.0010145444,0.0022323108,0.0009679221,0.018707173,0.15633745,0.010670075,0.09837041,0.00013516298],"about_ca_topic_score_codex":0.0014318151,"about_ca_topic_score_gemma":0.0052737715,"teacher_disagreement_score":0.0027126211,"about_ca_system_score_codex":0.00043296732,"about_ca_system_score_gemma":0.00039577624,"threshold_uncertainty_score":0.009074569},"labels":[],"label_agreement":null},{"id":"W3101884091","doi":"10.1038/s41588-020-00725-7","title":"Genome-wide association study of intracranial aneurysms identifies 17 risk loci and genetic overlap with clinical risk factors","year":2020,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Intracranial Aneurysms: Treatment and Complications","field":"Medicine","cited_by":346,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Jewish General Hospital; McGill University; Montreal Neurological Institute and Hospital","funders":"National Key Research and Development Program of China; European Regional Development Fund; Medical Research Council; Centre hospitalier régional universitaire de Lille; Schweizerische Akademie der Medizinischen Wissenschaften; Centers for Disease Control and Prevention; Biomedicum Helsinki-säätiö; Suomen Lääketieteen Säätiö; Päivikki ja Sakari Sohlbergin Säätiö; National Natural Science Foundation of China; Schweizerischer Nationalfonds zur Förderung der Wissenschaftlichen Forschung; Institut National de la Santé et de la Recherche Médicale; European Commission; Schweizerische Herzstiftung; Aarne ja Aili Turusen Säätiö; University of Oxford; National Institute of Neurological Disorders and Stroke; British Heart Foundation; Agence Nationale de la Recherche; Cancer Research UK; Wellcome Trust; Fondation de France; National Institute for Health and Care Research; Emil Aaltosen Säätiö; Maud Kuistilan Muistosäätiö; Alfred Kordelinin Säätiö; Aarne Koskelon Säätiö; Eli Lilly and Company; Canadian Institutes of Health Research; Uniwersytet Jagielloński Collegium Medicum; Helsingin ja Uudenmaan Sairaanhoitopiiri; GlaxoSmithKline; National Science Foundation","keywords":"Genome-wide association study; Genetic architecture; Biology; Subarachnoid hemorrhage; Aneurysm; Heritability; Pleiotropy; Genetic association; Disease; Quantitative trait locus; Genetics; Internal medicine; Single-nucleotide polymorphism; Gene; Medicine; Genotype; Surgery","score_opus":0.01515633204648634,"score_gpt":0.27743012594245187,"score_spread":0.2622737938959655,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W3101884091","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9954717,0.0014648995,0.001188487,0.00035459767,0.000043975804,0.000009636243,0.00039665625,0.000035561312,0.0010344826],"genre_scores_gemma":[0.9980585,0.0004092983,0.00083727733,0.00007287918,0.000054364595,0.000009505224,0.00028976885,0.000016263142,0.0002520818],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9984112,0.00056954595,0.0001664511,0.00042678075,0.0002433764,0.0001825916],"domain_scores_gemma":[0.99684024,0.0014033593,0.0009867691,0.00024877227,0.00018595277,0.00033481425],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0010067511,0.00090236234,0.00072043116,0.002149387,0.0007015052,0.0009635799,0.000810745,0.0014465764,0.0026927693],"category_scores_gemma":[0.00315851,0.00049529725,0.001270985,0.0029407819,0.00082984735,0.00033903745,0.00076149526,0.0010956331,0.00028205558],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0017506008,0.00012647214,0.97761256,0.000059836206,0.00172041,0.0017947285,0.00021477844,0.0002768878,0.008951203,0.00038205853,0.0005580356,0.0065525128],"study_design_scores_gemma":[0.00010991697,0.00012733931,0.99386615,0.000025518382,0.00082724873,0.002627274,0.00014553996,0.00059949333,0.00071440486,0.0004567031,0.0004826452,0.000017769888],"about_ca_topic_score_codex":0.0027694325,"about_ca_topic_score_gemma":0.0027540592,"teacher_disagreement_score":0.0027694325,"about_ca_system_score_codex":0.000253597,"about_ca_system_score_gemma":0.00051846605,"threshold_uncertainty_score":0.009008169},"labels":[],"label_agreement":null},{"id":"W3109183357","doi":"10.1038/s41588-020-00713-x","title":"Discovery of rare variants associated with blood pressure regulation through meta-analysis of 1.3 million individuals","year":2020,"lang":"en","type":"review","venue":"Nature Genetics","topic":"Genetic Associations and Epidemiology","field":"Biochemistry, Genetics and Molecular Biology","cited_by":239,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Université Laval; Population Health Research Institute; McMaster University","funders":"NHLBI Division of Intramural Research; National Institute of Diabetes and Digestive and Kidney Diseases; National Heart, Lung, and Blood Institute; NIHR Cambridge Biomedical Research Centre; NIHR Oxford Biomedical Research Centre; NIHR Imperial Biomedical Research Centre; Fonds de Recherche du Québec - Santé; Penn State College of Medicine; Steno Diabetes Center Aarhus; National Institutes of Health; MRC-PHE Centre for Environment and Health; Evans Medical Foundation; Novo Nordisk Fonden; Università degli Studi di Verona; Khalifa University of Science, Technology and Research; Pennsylvania State University; Lunds Universitet; Horizon 2020 Framework Programme; Universiteit Utrecht; Medical Research Council; Servier; University of Bristol; Imperial College London; National Human Genome Research Institute; Kidney Research UK; Department of Health and Social Care; University of Cambridge; British Heart Foundation; Stichting de Drie Lichten; Isaac Newton Trust; Eunice Kennedy Shriver National Institute of Child Health and Human Development; Barts Charity; U.S. Department of Health and Human Services; Genomic Health; Vanderbilt University Medical Center; National Cancer Institute; University College London; Cancer Research UK; Wellcome Trust; Gentofte Hospital; National Institute for Health and Care Research; University of North Carolina at Chapel Hill; Queen Mary University of London; Pfizer; University of Washington; National Institute on Minority Health and Health Disparities; AstraZeneca; Genentech; School of Public Health, Imperial College London; University of Oxford; Amgen; Novo Nordisk; Li Ka Shing Foundation; School of Medicine, Boston University; Cambridge University Hospitals; University of Pennsylvania; Vanderbilt University; International Seafood Sustainability Foundation; Biogen; Government of the United Kingdom; University of Michigan; UK Research and Innovation; Eli Lilly and Company","keywords":"Biology; Meta-analysis; Computational biology; Genetics; Blood pressure; Evolutionary biology; Bioinformatics; Internal medicine; Endocrinology; Medicine","score_opus":0.04167368506031807,"score_gpt":0.3203020398534679,"score_spread":0.27862835479314985,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W3109183357","genre_codex":"review","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":null,"domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.0009531418,0.99688476,0.0006367512,0.00068645226,0.0002478139,0.000005550147,0.0002647058,0.000023383553,0.0002974292],"genre_scores_gemma":[0.008819527,0.9866252,0.0015849251,0.0013037418,0.0005834429,0.000021267519,0.00064061803,0.000017070688,0.0004041601],"study_design_codex":"design_other","study_design_gemma":"meta_analysis","domain_scores_codex":[0.9993193,0.00020880261,0.00011632372,0.00016552812,0.00014533005,0.00004476863],"domain_scores_gemma":[0.9979978,0.0014857342,0.00020166971,0.00007238159,0.00018143792,0.000060905568],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0023244116,0.0009722105,0.0024301556,0.0012241511,0.000114003175,0.0009117941,0.0010187334,0.0010538553,0.0019995768],"category_scores_gemma":[0.003666303,0.00036489067,0.002191248,0.001757817,0.00025150503,0.0004716066,0.0007097066,0.0013299977,0.00058696815],"study_design_candidate":"meta_analysis","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0011773738,0.00004931608,0.010480851,0.03701863,0.021103185,0.0010780003,0.00009852954,0.0007685038,0.0026498544,0.0026705903,0.030161573,0.8927436],"study_design_scores_gemma":[0.0014198965,0.00078481465,0.08509086,0.02977059,0.100259356,0.010379777,0.00022934529,0.0012557327,0.0029992834,0.018971898,0.7485139,0.00032452215],"about_ca_topic_score_codex":0.0015406441,"about_ca_topic_score_gemma":0.0034348217,"teacher_disagreement_score":0.0024301556,"about_ca_system_score_codex":0.00033841198,"about_ca_system_score_gemma":0.0014338174,"threshold_uncertainty_score":0.012292862},"labels":[],"label_agreement":null},{"id":"W3113754461","doi":"10.1038/s41588-021-00923-x","title":"Genomic and phenotypic insights from an atlas of genetic effects on DNA methylation","year":2021,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Epigenetics and DNA Methylation","field":"Biochemistry, Genetics and Molecular Biology","cited_by":539,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"SickKids Foundation; Hospital for Sick Children; Public Health Ontario; University of Toronto","funders":"Economic and Social Research Council; Medical Research Council; Directorate for Biological Sciences; Nederlandse Federatie van Universitair Medische Centra; Biotechnology and Biological Sciences Research Council; ZonMw; Österreichischen Akademie der Wissenschaften; Wellcome Trust; Agence Nationale de la Recherche; Research Councils UK; Motor Neurone Disease Association; National Institute for Health and Care Research; University of Bristol; Joint Programming Initiative A healthy diet for a healthy life; Cancer Research UK; British Heart Foundation; Royal Society; Wellcome","keywords":"Biology; DNA methylation; Genetics; Phenotype; Computational biology; Evolutionary biology; Gene; Gene expression","score_opus":0.005549023439395979,"score_gpt":0.24853984928658718,"score_spread":0.2429908258471912,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W3113754461","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.8169011,0.004507545,0.13886893,0.0013072821,0.00027472418,0.000046991,0.008846808,0.0028841,0.026362494],"genre_scores_gemma":[0.9582061,0.0025381504,0.023301106,0.00025450913,0.000053228534,0.00003903735,0.0021842865,0.0004329961,0.012990479],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.99989474,0.000011976732,0.000004834489,0.000029995721,0.000038463913,0.00001990538],"domain_scores_gemma":[0.9998142,0.0000426214,0.000030456682,0.00004983488,0.000022703378,0.00004019251],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00017355754,0.0002360667,0.00025201848,0.00087105477,0.0002562377,0.0005536653,0.0003724516,0.00032007668,0.004350112],"category_scores_gemma":[0.00022856354,0.00024832573,0.00027180507,0.0005367131,0.00032802275,0.00042005052,0.00052503584,0.00075858185,0.0007500223],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00009065986,0.000006986506,0.000735346,0.000029515531,0.000012591252,0.00014339639,0.000020736708,0.0006327024,0.98757577,0.002888162,0.00033975783,0.0075243837],"study_design_scores_gemma":[0.000022712904,0.00012653186,0.04600546,0.000012569831,0.00008306166,0.0016018458,0.00008683859,0.0045914142,0.9171828,0.0063576875,0.023889028,0.000039997878],"about_ca_topic_score_codex":0.0010470438,"about_ca_topic_score_gemma":0.0022430643,"teacher_disagreement_score":0.004350112,"about_ca_system_score_codex":0.00037500542,"about_ca_system_score_gemma":0.0002212501,"threshold_uncertainty_score":0.014552593},"labels":[],"label_agreement":null},{"id":"W3114958691","doi":"10.1038/s41588-020-00760-4","title":"Author Correction: Genome-wide association study of intracranial aneurysms identifies 17 risk loci and genetic overlap with clinical risk factors","year":2020,"lang":"en","type":"erratum","venue":"Nature Genetics","topic":"Folate and B Vitamins Research","field":"Medicine","cited_by":6,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Jewish General Hospital; McGill University; Montreal Neurological Institute and Hospital","funders":"National Institute of Neurological Disorders and Stroke; Medical Research Council; Société Française de Radiologie; Institut National de la Santé et de la Recherche Médicale; Agence Nationale de la Recherche; British Heart Foundation","keywords":"Biology; Genome-wide association study; Genetic association; Computational biology; Association (psychology); Genetics; Evolutionary biology; Single-nucleotide polymorphism; Gene; Epistemology; Genotype","score_opus":0.018832946015912785,"score_gpt":0.32325893964499447,"score_spread":0.3044259936290817,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W3114958691","genre_codex":"editorial","genre_gemma":"other","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"other","genre_consensus":null,"domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.00016492074,0.00051518314,0.00066726113,0.041993044,0.9535574,0.000020600104,0.0015484657,0.0003318863,0.0012012761],"genre_scores_gemma":[0.024799708,0.0056963013,0.012160103,0.12991817,0.60979784,0.00036748618,0.006246041,0.0028337035,0.20818065],"study_design_codex":"not_applicable","study_design_gemma":"not_applicable","domain_scores_codex":[0.99475783,0.0010312531,0.0010255495,0.0008436309,0.0018054104,0.000536335],"domain_scores_gemma":[0.9634689,0.010702697,0.0020467062,0.0022972443,0.019547613,0.0019368136],"candidate_categories":["research_integrity"],"consensus_categories":[],"category_scores_codex":[0.005687975,0.003010315,0.0028793006,0.004313764,0.0032294637,0.004006096,0.005585135,0.009328203,0.073274024],"category_scores_gemma":[0.07471238,0.0019371657,0.0024861062,0.0026032361,0.0022004617,0.0020637254,0.0020298634,0.0131939845,0.026733514],"study_design_candidate":"not_applicable","study_design_consensus":"not_applicable","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.000057828012,0.0000061148867,0.0001702364,0.00011370424,0.00003316732,0.0005340139,0.000024197398,0.00004171353,0.000040193667,0.00041039143,0.9958026,0.002765903],"study_design_scores_gemma":[0.0004862396,0.000057334426,0.003465703,0.0009714276,0.0003450317,0.004494743,0.00020760729,0.0009298893,0.00076418865,0.00403053,0.9841022,0.00014505313],"about_ca_topic_score_codex":0.026069675,"about_ca_topic_score_gemma":0.03545756,"teacher_disagreement_score":0.9906718,"about_ca_system_score_codex":0.0037806267,"about_ca_system_score_gemma":0.0069327434,"threshold_uncertainty_score":0.24512601},"labels":[],"label_agreement":null},{"id":"W3115151307","doi":"10.1038/s41588-020-00748-0","title":"Trans-ancestry genome-wide association meta-analysis of prostate cancer identifies new susceptibility loci and informs genetic risk prediction","year":2021,"lang":"en","type":"review","venue":"Nature Genetics","topic":"Genetic Associations and Epidemiology","field":"Biochemistry, Genetics and Molecular Biology","cited_by":500,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Alberta; Université de Montréal; Princess Margaret Cancer Centre; Institut National de la Recherche Scientifique; University of Toronto","funders":"Medical Research Council; European Society for Medical Oncology; National Cancer Institute; National Institutes of Health; U.S. Department of Health and Human Services; Cancer Research UK; Wellcome Trust; National Institute of Environmental Health Sciences; Ipsen; National Institute for Health and Care Research; Achievement Rewards for College Scientists Foundation","keywords":"Prostate cancer; Odds ratio; Biology; Genome-wide association study; Genetic genealogy; Population; Confidence interval; Demography; Genetics; Cancer; Oncology; Internal medicine; Single-nucleotide polymorphism; Medicine; Genotype; Gene","score_opus":0.03240215357334369,"score_gpt":0.33018350076577246,"score_spread":0.29778134719242877,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W3115151307","genre_codex":"review","genre_gemma":"review","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"review","genre_consensus":"review","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.0000817762,0.9992902,0.00015206158,0.00025885916,0.000053809395,0.000002283496,0.000024607065,0.000006564879,0.00012980642],"genre_scores_gemma":[0.0011968325,0.9980262,0.00029135167,0.00021193111,0.00009019484,0.000006140669,0.0000634968,0.0000028540728,0.00011100388],"study_design_codex":"design_other","study_design_gemma":"meta_analysis","domain_scores_codex":[0.9992705,0.00030730185,0.000085102845,0.00013529258,0.00015594788,0.00004595466],"domain_scores_gemma":[0.99802434,0.0014681125,0.000166093,0.000049927457,0.00022203625,0.00006958951],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0025471286,0.001318197,0.0039669005,0.0028004968,0.00017482783,0.001157252,0.0014541723,0.0013687231,0.0025233557],"category_scores_gemma":[0.0040074564,0.0004211933,0.0024535602,0.0034102777,0.0003770018,0.00082461763,0.00080108293,0.0020381894,0.00079786277],"study_design_candidate":"meta_analysis","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0003276083,0.000036432662,0.0015564243,0.037148934,0.008587477,0.00020899472,0.00004460623,0.00079618534,0.0005239511,0.0022034165,0.02195477,0.92661124],"study_design_scores_gemma":[0.0005288188,0.00052424,0.02240301,0.055095475,0.038570482,0.003570804,0.00018809,0.0014377369,0.0015050013,0.019099098,0.85687166,0.00020568985],"about_ca_topic_score_codex":0.002355661,"about_ca_topic_score_gemma":0.0053972285,"teacher_disagreement_score":0.0039669005,"about_ca_system_score_codex":0.0008571041,"about_ca_system_score_gemma":0.0017579576,"threshold_uncertainty_score":0.01347065},"labels":[],"label_agreement":null},{"id":"W3118751020","doi":"10.1038/s41588-020-00754-2","title":"Investigating the genetic architecture of noncognitive skills using GWAS-by-subtraction","year":2021,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Genetic Associations and Epidemiology","field":"Biochemistry, Genetics and Molecular Biology","cited_by":297,"is_retracted":false,"has_abstract":false,"route_ca_aff":false,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"","funders":"National Institute on Minority Health and Health Disparities; National Institute of Child Health and Human Development; National Institute of Mental Health; National Institute on Aging; National Institutes of Health; Avera Institute for Human Genetics; Jacobs Foundation; ZonMw; Medical Research Council; Koninklijke Nederlandse Akademie van Wetenschappen; Eunice Kennedy Shriver National Institute of Child Health and Human Development; Economic and Social Research Council; European Commission; Stichting Volksbond Rotterdam; AXA Research Fund; Canadian Institute for Advanced Research; North Carolina Biotechnology Center; Nederlandse Organisatie voor Wetenschappelijk Onderzoek; Sage Foundation; University of Texas at Austin","keywords":"Genome-wide association study; Genetic architecture; Educational attainment; Cognition; Biology; Genetic association; Association (psychology); Behavioural genetics; Big Five personality traits; Genetics; Personality; Psychology; Single-nucleotide polymorphism; Phenotype; Neuroscience; Genotype; Social psychology","score_opus":0.008837250089870172,"score_gpt":0.28112396487396246,"score_spread":0.2722867147840923,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W3118751020","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.95712006,0.0013916075,0.034738626,0.00064873917,0.00021724726,0.000074867006,0.0028350751,0.0002883204,0.002685418],"genre_scores_gemma":[0.9911103,0.00026526744,0.006547784,0.00013707209,0.000061394756,0.00004555762,0.00081640517,0.00010237813,0.00091383833],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99399626,0.0027348467,0.00048068594,0.0017581738,0.0006211418,0.00040876603],"domain_scores_gemma":[0.9911833,0.004927935,0.0012379412,0.0017894255,0.0005056058,0.00035587198],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.005531644,0.0016951712,0.0011678648,0.002566792,0.0010920818,0.0018717375,0.0014793897,0.0012659939,0.006254404],"category_scores_gemma":[0.012165298,0.0007103826,0.0031550333,0.0036865931,0.0008159979,0.0010341569,0.0014825941,0.0016186645,0.0006525372],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0016011051,0.00014864013,0.9448991,0.0001795151,0.009455457,0.0010845016,0.0003910175,0.0016692564,0.013519037,0.0038432495,0.0013318096,0.02187727],"study_design_scores_gemma":[0.00020693071,0.00055066735,0.96299034,0.00006669445,0.0037384701,0.0025354805,0.000502829,0.010669968,0.004724724,0.009095145,0.0048498902,0.00006897871],"about_ca_topic_score_codex":0.009137416,"about_ca_topic_score_gemma":0.009446043,"teacher_disagreement_score":0.009137416,"about_ca_system_score_codex":0.0003435377,"about_ca_system_score_gemma":0.000823965,"threshold_uncertainty_score":0.029254436},"labels":[],"label_agreement":null},{"id":"W3119083026","doi":"10.1038/s41588-021-00780-8","title":"Author Correction: Mutations disrupting neuritogenesis genes confer risk for cerebral palsy","year":2021,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Cerebral Palsy and Movement Disorders","field":"Medicine","cited_by":5,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Centre for Addiction and Mental Health","funders":"","keywords":"Biology; Cerebral palsy; Gene; Genetics; Physical medicine and rehabilitation; Medicine","score_opus":0.019690542838866607,"score_gpt":0.3112674968220634,"score_spread":0.2915769539831968,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W3119083026","genre_codex":"editorial","genre_gemma":"other","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"other","genre_consensus":null,"domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.001387052,0.00088689534,0.0022458031,0.049332324,0.940451,0.000036920013,0.0011908758,0.00096739293,0.0035017428],"genre_scores_gemma":[0.16029717,0.008680632,0.028426426,0.08479789,0.35854587,0.0004260347,0.0055175065,0.005471072,0.3478374],"study_design_codex":"not_applicable","study_design_gemma":"not_applicable","domain_scores_codex":[0.99616313,0.00048443422,0.0005862306,0.00067052286,0.0015742598,0.0005213551],"domain_scores_gemma":[0.9830162,0.005406529,0.0013629908,0.0015177663,0.007194869,0.001501651],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.002310563,0.0021590577,0.0025096256,0.0029240989,0.003165425,0.0029849766,0.0047405562,0.011267014,0.054955438],"category_scores_gemma":[0.033938542,0.0013549725,0.001874429,0.0016867917,0.002077724,0.0016497312,0.0021636405,0.008454632,0.01976865],"study_design_candidate":"not_applicable","study_design_consensus":"not_applicable","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00011148765,0.000018707857,0.00051686104,0.0003099648,0.000091550915,0.009772772,0.00008405383,0.0002866498,0.00067183864,0.0019666236,0.9740993,0.012070202],"study_design_scores_gemma":[0.00026496095,0.00007172899,0.0029386824,0.00045892896,0.00022492369,0.026023975,0.00025489184,0.0018383675,0.0034573195,0.003331313,0.9610126,0.00012226602],"about_ca_topic_score_codex":0.007804349,"about_ca_topic_score_gemma":0.009894667,"teacher_disagreement_score":0.054955438,"about_ca_system_score_codex":0.0028760745,"about_ca_system_score_gemma":0.0034343223,"threshold_uncertainty_score":0.18384427},"labels":[],"label_agreement":null},{"id":"W3119731794","doi":"10.1038/s41588-020-00742-6","title":"Toward better governance of human genomic data","year":2021,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Ethics in Clinical Research","field":"Medicine","cited_by":65,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Council of Canadian Academies; McGill University; University of British Columbia, Okanagan Campus; University of British Columbia; University of Guelph","funders":"Eunice Kennedy Shriver National Institute of Child Health and Human Development; National Institute of Child Health and Human Development; National Institute of Diabetes and Digestive and Kidney Diseases; National Center on Minority Health and Health Disparities; Wellcome Trust; National Human Genome Research Institute; National Heart, Lung, and Blood Institute; Norges Forskningsråd; National Institute on Minority Health and Health Disparities; Japan Agency for Medical Research and Development; NordForsk; National Science Foundation; Canadian Institutes of Health Research; Genome Canada; National Cancer Institute; National Institutes of Health","keywords":"Corporate governance; Biology; Data science; Key (lock); Business; Computer science; Ecology","score_opus":0.3832454896893916,"score_gpt":0.550342508910356,"score_spread":0.16709701922096437,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W3119731794","genre_codex":"commentary","genre_gemma":"methods","domain_codex":null,"domain_gemma":"methods","model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"methods","genre_consensus":null,"domain_candidate":"methods","domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.007651234,0.002568279,0.14749932,0.7910971,0.0021963592,0.0002646543,0.00011207955,0.00030375455,0.048307166],"genre_scores_gemma":[0.58097583,0.0039190273,0.11722876,0.2652809,0.009343273,0.001269007,0.00044700986,0.0006515937,0.020884562],"study_design_codex":"theoretical_or_conceptual","study_design_gemma":"theoretical_or_conceptual","domain_scores_codex":[0.6950344,0.24540535,0.0090371445,0.012441738,0.027566347,0.010514951],"domain_scores_gemma":[0.48308417,0.32989436,0.024169464,0.07468595,0.053738244,0.03442783],"candidate_categories":["metaresearch"],"consensus_categories":["metaresearch"],"category_scores_codex":[0.29094687,0.00072411017,0.0016840245,0.0030564913,0.0052248226,0.026523346,0.005251692,0.020018628,0.006255984],"category_scores_gemma":[0.36547872,0.0013299449,0.0013856508,0.0033149314,0.031707365,0.023101686,0.01779987,0.032308735,0.0017898056],"study_design_candidate":"theoretical_or_conceptual","study_design_consensus":"theoretical_or_conceptual","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.000030430647,0.000062465006,0.0022947683,0.00009713524,0.00006539586,0.0001564543,0.003456531,0.0017342381,0.00038025234,0.9308254,0.038366944,0.022529878],"study_design_scores_gemma":[0.000048822007,0.000028223127,0.0009792093,0.00031090697,0.000021750588,0.00010881592,0.0010153264,0.0021408712,0.00037207533,0.9038993,0.09103023,0.000044456418],"about_ca_topic_score_codex":0.006916227,"about_ca_topic_score_gemma":0.0076087997,"teacher_disagreement_score":0.70905316,"about_ca_system_score_codex":0.012644984,"about_ca_system_score_gemma":0.061259814,"threshold_uncertainty_score":0.87438875},"labels":[],"label_agreement":null},{"id":"W3121184362","doi":"10.1038/s41588-020-00762-2","title":"Shared genetic pathways contribute to risk of hypertrophic and dilated cardiomyopathies with opposite directions of effect","year":2021,"lang":"en","type":"review","venue":"Nature Genetics","topic":"Cardiomyopathy and Myosin Studies","field":"Medicine","cited_by":292,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Western University; Université de Montréal; Montreal Heart Institute","funders":"National Cancer Institute; NIH Office of the Director; National Institute on Drug Abuse; NIHR Oxford Biomedical Research Centre; Engineering and Physical Sciences Research Council; Medical Research Council; Canadian Institutes of Health Research; Amsterdam Cardiovascular Sciences, Amsterdam University Medical Centers; National Institute of Mental Health; Horizon 2020 Framework Programme; Mason Medical Research Trust; Klaus Tschira Stiftung; Wellcome Trust; Imperial College Healthcare NHS Trust; BHF Centre of Research Excellence, Oxford; Stichting Volksbond Rotterdam; Fédération Française de Cardiologie; Università degli Studi di Firenze; ZonMw; Common Fund; Netherlands Heart Institute; Japan Society for the Promotion of Science; Deutsches Zentrum für Herz-Kreislaufforschung; Heart Rhythm Society; Imperial College London; Fondation Institut de Cardiologie de Montréal; UK Research and Innovation; National Institute for Health and Care Research; Agence Nationale de la Recherche; Fondation Leducq; National Human Genome Research Institute; UK Dementia Research Institute; Amsterdam University Medical Centers; National Institutes of Health; European Research Area Network on Cardiovascular Diseases; Rosetrees Trust; European Commission; European Society of Cardiology; National Heart, Lung, and Blood Institute; Academy of Medical Sciences; National Institute of Neurological Disorders and Stroke; British Heart Foundation; Institut de Cardiologie de Montréal; Heart and Stroke Foundation of Canada","keywords":"Hypertrophic cardiomyopathy; Dilated cardiomyopathy; Genome-wide association study; Mendelian randomization; Internal medicine; Biology; Cardiology; Heart failure; Biobank; Genetics; Genotype; Genetic variants; Gene; Medicine; Single-nucleotide polymorphism","score_opus":0.013125052207083272,"score_gpt":0.2773408998950582,"score_spread":0.26421584768797496,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W3121184362","genre_codex":"review","genre_gemma":"review","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"review","genre_consensus":"review","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.00044449893,0.99802905,0.0002773125,0.00039894172,0.0001426282,0.0000028084128,0.00004359317,0.000007490572,0.0006535908],"genre_scores_gemma":[0.0033092508,0.99497956,0.00050649064,0.00031463147,0.00039963936,0.0000069884104,0.000081582926,0.000001964236,0.00039994935],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.99979144,0.00004482786,0.000031785952,0.00006426183,0.000052426018,0.000015173422],"domain_scores_gemma":[0.9994923,0.0003555297,0.000060507606,0.000012856904,0.0000581032,0.00002065927],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00055748434,0.0009317501,0.0016905947,0.0011358097,0.00011154242,0.00064898405,0.00067560165,0.0010445556,0.0022230144],"category_scores_gemma":[0.0011135706,0.00016755254,0.00068262353,0.0010834365,0.00034609667,0.00043348313,0.0004582629,0.00093069195,0.00048694416],"study_design_candidate":"not_applicable","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00042437325,0.000056600642,0.0044708955,0.01407833,0.0014281082,0.0011891156,0.000055698794,0.0004925159,0.0025067986,0.0053504766,0.015258546,0.9546885],"study_design_scores_gemma":[0.0004404873,0.00045725986,0.040299546,0.022898458,0.00893191,0.016566738,0.00030755444,0.000623479,0.0022719908,0.021567658,0.88546634,0.00016852126],"about_ca_topic_score_codex":0.00073371513,"about_ca_topic_score_gemma":0.0009917902,"teacher_disagreement_score":0.0022230144,"about_ca_system_score_codex":0.00026766496,"about_ca_system_score_gemma":0.0005653266,"threshold_uncertainty_score":0.0074367523},"labels":[],"label_agreement":null},{"id":"W3121407008","doi":"10.1038/s41588-020-00763-1","title":"Large-scale association analyses identify host factors influencing human gut microbiome composition","year":2021,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Gut microbiota and health","field":"Biochemistry, Genetics and Molecular Biology","cited_by":1832,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Hospital for Sick Children; University of Toronto; Mount Sinai Hospital","funders":"National Institute on Minority Health and Health Disparities; National Center for Advancing Translational Sciences; Wellcome Trust; Nederlandse Organisatie voor Wetenschappelijk Onderzoek; National Human Genome Research Institute; National Institute of Diabetes and Digestive and Kidney Diseases; National Heart, Lung, and Blood Institute; National Institute of Mental Health; Medical Research Council; Cancer Research UK; Novo Nordisk Fonden; National Institute of Neurological Disorders and Stroke; National Institute for Health and Care Research; Lundbeckfonden","keywords":"Biology; Microbiome; Host (biology); Gut microbiome; Scale (ratio); Computational biology; Evolutionary biology; Genetics","score_opus":0.013447417327125778,"score_gpt":0.3366232818866221,"score_spread":0.3231758645594963,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W3121407008","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9919408,0.0022308982,0.0038383775,0.0003297293,0.00005408962,0.000010219783,0.0009048667,0.00006021636,0.00063093536],"genre_scores_gemma":[0.9973029,0.00032505905,0.001554282,0.000097800556,0.00003234441,0.000010994708,0.00034631425,0.000033292454,0.0002971283],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9976641,0.0011804576,0.00012753479,0.0006151099,0.00022770469,0.00018512807],"domain_scores_gemma":[0.9954548,0.002357511,0.0009417304,0.00071660633,0.00019563238,0.0003336927],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0023142716,0.00061413326,0.0006281643,0.0011669686,0.0006988735,0.0012975112,0.00047142553,0.0007883996,0.002358783],"category_scores_gemma":[0.0050612353,0.00036771188,0.0012428719,0.0020531954,0.000679532,0.00042529733,0.0010314446,0.0011010247,0.0002769019],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0018738387,0.00012866716,0.94203186,0.00012282086,0.0041168053,0.0004501171,0.0002463421,0.00052620634,0.033984207,0.0004377605,0.00069883646,0.015382484],"study_design_scores_gemma":[0.00004760797,0.00013726526,0.9938871,0.00001788586,0.0009787498,0.0004708501,0.00015801803,0.0012726273,0.0015300988,0.00066343514,0.00081728835,0.000018998391],"about_ca_topic_score_codex":0.0020071235,"about_ca_topic_score_gemma":0.0041008443,"teacher_disagreement_score":0.002358783,"about_ca_system_score_codex":0.0001766796,"about_ca_system_score_gemma":0.00039703216,"threshold_uncertainty_score":0.012239158},"labels":[],"label_agreement":null},{"id":"W3122115907","doi":"10.1038/s41588-020-00764-0","title":"Common genetic variants and modifiable risk factors underpin hypertrophic cardiomyopathy susceptibility and expressivity","year":2021,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Cardiomyopathy and Myosin Studies","field":"Medicine","cited_by":339,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Calgary; Foothills Medical Centre; Montreal Heart Institute; University Health Network; University of Toronto; Royal Victoria Hospital; McGill University Health Centre; Université Laval; Royal Victoria Regional Health Centre","funders":"National Heart, Lung, and Blood Institute; Medical Research Council; European Commission; Department of Health and Social Care; National Institute for Health and Care Research; National Institutes of Health; U.S. Department of Health and Human Services; NIHR BioResource; Novo Nordisk Fonden; Cancer Research UK; Biomedical Research Council; British Heart Foundation; NIHR Oxford Biomedical Research Centre; Wellcome Trust; Wellcome; NHS Blood and Transplant","keywords":"Hypertrophic cardiomyopathy; Biology; Genome-wide association study; Genetics; Mendelian randomization; Odds ratio; Sarcomere; Single-nucleotide polymorphism; Candidate gene; Internal medicine; Genotype; Gene; Medicine; Genetic variants; Endocrinology","score_opus":0.01456130707113004,"score_gpt":0.2599788649890439,"score_spread":0.24541755791791384,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W3122115907","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9927912,0.0017895538,0.0019879946,0.0003619391,0.00005068543,0.0000148895715,0.00027132014,0.000025787593,0.0027066437],"genre_scores_gemma":[0.9980275,0.00040558845,0.0006235095,0.00006659311,0.00007771095,0.000008642013,0.00012715998,0.000022057679,0.0006411802],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99899834,0.0002964383,0.00010231043,0.00029746117,0.00015568404,0.00014978871],"domain_scores_gemma":[0.9975948,0.0010063804,0.0006973082,0.0003158459,0.00014958241,0.00023600196],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0011978032,0.0008199368,0.0005334861,0.0018740864,0.00062963733,0.0011012717,0.00094630854,0.0010743933,0.0051388238],"category_scores_gemma":[0.004067554,0.0004513922,0.0007106263,0.001191806,0.0011326936,0.00082057505,0.0010607439,0.0011381252,0.0003584696],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00084046164,0.000088439236,0.94547087,0.000070323884,0.0005618389,0.002678951,0.00087848003,0.00022838588,0.034621038,0.0022235594,0.00028920118,0.012048481],"study_design_scores_gemma":[0.000020010195,0.000098888086,0.9910308,0.00006418731,0.00024752395,0.0025995676,0.0005257016,0.00042416566,0.0020610911,0.0023155923,0.00059194496,0.000020440133],"about_ca_topic_score_codex":0.0018228994,"about_ca_topic_score_gemma":0.0017608334,"teacher_disagreement_score":0.0051388238,"about_ca_system_score_codex":0.00023382572,"about_ca_system_score_gemma":0.0002484927,"threshold_uncertainty_score":0.017191052},"labels":[],"label_agreement":null},{"id":"W3122758506","doi":"10.1038/s41588-021-00786-2","title":"Publisher Correction: Trans-ancestry genome-wide association meta-analysis of prostate cancer identifies new susceptibility loci and informs genetic risk prediction","year":2021,"lang":"en","type":"erratum","venue":"Nature Genetics","topic":"Molecular Biology Techniques and Applications","field":"Biochemistry, Genetics and Molecular Biology","cited_by":13,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Alberta; Université de Montréal; Princess Margaret Cancer Centre; Institut National de la Recherche Scientifique; University of Toronto","funders":"Cancer Research UK; U.S. Department of Veterans Affairs","keywords":"Biology; Genome-wide association study; Prostate cancer; Genetics; Meta-analysis; Genetic association; Genetic genealogy; Computational biology; Evolutionary biology; Single-nucleotide polymorphism; Cancer; Genotype; Gene; Demography; Internal medicine; Population; Medicine","score_opus":0.012006874919037387,"score_gpt":0.2762989504037336,"score_spread":0.2642920754846962,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W3122758506","genre_codex":"editorial","genre_gemma":"other","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"other","genre_consensus":null,"domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.00011991975,0.00069825567,0.0009743881,0.03238132,0.96025246,0.000026006388,0.0026573054,0.00047769415,0.002412632],"genre_scores_gemma":[0.020872148,0.006421399,0.012737105,0.108297035,0.41848972,0.0005234257,0.008939682,0.00569255,0.41802698],"study_design_codex":"not_applicable","study_design_gemma":"not_applicable","domain_scores_codex":[0.9935448,0.0012974024,0.0013219371,0.00090292655,0.0025028368,0.00043015377],"domain_scores_gemma":[0.9434103,0.01567023,0.0021818858,0.005468301,0.031288307,0.0019809625],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.007625582,0.0026191967,0.003086885,0.005317812,0.003445102,0.0051254937,0.0050291843,0.0060335738,0.101553254],"category_scores_gemma":[0.108651266,0.0020450572,0.0024629696,0.004079029,0.002033971,0.0023697386,0.0022341444,0.0114174355,0.043395936],"study_design_candidate":"not_applicable","study_design_consensus":"not_applicable","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00002930563,0.000003455282,0.00009993924,0.00010839243,0.000027522372,0.00018478803,0.000017264718,0.00004373536,0.000021520389,0.0004052292,0.9954945,0.003564487],"study_design_scores_gemma":[0.00015606899,0.00002201067,0.0018082361,0.00068475475,0.00019957415,0.0012045185,0.00009293247,0.00056293065,0.0003997077,0.003389373,0.99139565,0.00008441335],"about_ca_topic_score_codex":0.030147431,"about_ca_topic_score_gemma":0.04265391,"teacher_disagreement_score":0.101553254,"about_ca_system_score_codex":0.0038962879,"about_ca_system_score_gemma":0.006870019,"threshold_uncertainty_score":0.3397295},"labels":[],"label_agreement":null},{"id":"W3128153416","doi":"10.1038/s41588-021-00785-3","title":"Genome sequencing analysis identifies new loci associated with Lewy body dementia and provides insights into its genetic architecture","year":2021,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Neurological diseases and metabolism","field":"Neuroscience","cited_by":481,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Heart and Stroke Foundation; Sunnybrook Health Science Centre; Occupational Cancer Research Centre; Health Sciences Centre; McGill University; Montreal Neurological Institute and Hospital; University of Toronto","funders":"Administration for Native Americans; Takeda Pharmaceuticals U.S.A.; National Human Genome Research Institute; Demensförbundet; National Heart, Lung, and Blood Institute; National Institute of Neurological Disorders and Stroke; Department of Medicine, University of Toronto; King's College London; Centre National de la Recherche Scientifique; European Regional Development Fund; National Center for Advancing Translational Sciences; Medical Research Council; University at Buffalo; National Institutes of Health; Instituto de Investigación Marqués de Valdecilla; H. Lundbeck A/S; University of Bristol; Idorsia Pharmaceuticals; Johns Hopkins University; Centro de Investigación Biomédica en Red sobre Enfermedades Neurodegenerativas; Imperial College London; University of Toronto; Institut National de la Santé et de la Recherche Médicale; Parkinson's UK; Charles F. and Joanne Knight Alzheimer Disease Research Center, Washington University in St. Louis; Newcastle University; National Institute on Aging; National Institute for Health and Care Research; Biogen; Agence Nationale de la Recherche; Sol Goldman Charitable Trust; American Parkinson Disease Association; Consortium canadien en neurodégénérescence associée au vieillissement; Prothena; Northwestern University; Sunnybrook Research Institute; Little Family Foundation; Center for Individualized Medicine, Mayo Clinic; Institute of Psychiatry, Psychology and Neuroscience, King’s College London; Lewy Body Dementia Association; Wellcome Trust; Feinberg School of Medicine; Virginia Commonwealth University; Eli Lilly and Company; Sorbonne Université; Theravance Biopharma US; U.S. Department of Health and Human Services; Foundation for the National Institutes of Health","keywords":"Biology; Genetic architecture; Computational biology; Lewy body; Genome-wide association study; Genetics; Genome; DNA sequencing; Dementia; Evolutionary biology; Gene; Quantitative trait locus; Disease; Single-nucleotide polymorphism; Genotype","score_opus":0.014244459542587814,"score_gpt":0.24683899603309953,"score_spread":0.2325945364905117,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W3128153416","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.98404294,0.0021600304,0.009254843,0.00027481312,0.000030180636,0.000032946627,0.002748691,0.0000999014,0.0013555444],"genre_scores_gemma":[0.97892433,0.0021401427,0.011691031,0.00031833083,0.000039927112,0.00003081638,0.005845234,0.000036780093,0.00097351416],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.99980396,0.00003130137,0.000017087408,0.00008268248,0.000043517535,0.000021514921],"domain_scores_gemma":[0.99953365,0.00018474978,0.00014050331,0.000036249272,0.000049483515,0.000055382025],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00043523023,0.00047232985,0.00035584753,0.0014688413,0.00037739336,0.0005649083,0.00023647849,0.00047595182,0.0009797679],"category_scores_gemma":[0.00065950875,0.00017280043,0.00033732515,0.00088800414,0.00021559597,0.00019262049,0.00038471344,0.00039472085,0.00022424397],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0013192409,0.00023412173,0.40766835,0.000499083,0.0014028735,0.0059895795,0.0010638458,0.0031038832,0.4791438,0.002174685,0.0016873316,0.095713176],"study_design_scores_gemma":[0.00005745756,0.00030143443,0.9483141,0.000093174815,0.0004896102,0.005938238,0.00029792235,0.0034795196,0.02976625,0.002296943,0.008915698,0.000049683516],"about_ca_topic_score_codex":0.0023006082,"about_ca_topic_score_gemma":0.008450336,"teacher_disagreement_score":0.0023006082,"about_ca_system_score_codex":0.00019181811,"about_ca_system_score_gemma":0.00027384958,"threshold_uncertainty_score":0.0045744777},"labels":[],"label_agreement":null},{"id":"W3128359329","doi":"10.1038/s41588-020-00770-2","title":"Metabolic control of DNA methylation in naive pluripotent cells","year":2021,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Epigenetics and DNA Methylation","field":"Biochemistry, Genetics and Molecular Biology","cited_by":60,"is_retracted":false,"has_abstract":false,"route_ca_aff":false,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"","funders":"Institute of Genetics; Biotechnology and Biological Sciences Research Council; Ministero dell’Istruzione, dell’Università e della Ricerca; Medical Research Council; Giovanni Armenise-Harvard Foundation; Associazione Italiana per la Ricerca sul Cancro; European Foundation for the Study of Diabetes; Università degli Studi di Milano; Eli Lilly and Company","keywords":"Biology; DNA methylation; DNMT3B; Epigenetics; Methylation; Epigenome; Cell biology; Epiblast; Molecular biology; Embryonic stem cell; Genetics; Gene expression; Gene; Gastrulation","score_opus":0.005880120046647593,"score_gpt":0.24893375086524064,"score_spread":0.24305363081859305,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W3128359329","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9688599,0.004084677,0.019579962,0.00060362567,0.000121504854,0.000020408741,0.0011305042,0.00018721801,0.005412234],"genre_scores_gemma":[0.9918549,0.000838446,0.0033511561,0.00007478049,0.00001827932,0.000011449918,0.0005741304,0.0000325664,0.003244213],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99983275,0.00003615246,0.000013563083,0.000043704742,0.000049570124,0.00002419115],"domain_scores_gemma":[0.99984694,0.000031159867,0.000030188623,0.000026134103,0.000027888645,0.00003771999],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00019743128,0.00016406825,0.00021041046,0.00020914814,0.00020777728,0.0006676443,0.0002965217,0.0003003282,0.0009969173],"category_scores_gemma":[0.000261207,0.00016069345,0.00018632362,0.00017946311,0.0002325939,0.00036895194,0.00030691124,0.00057319034,0.00027674355],"study_design_candidate":"bench_or_experimental","study_design_consensus":"bench_or_experimental","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00013435168,0.0000058900787,0.00044218285,0.000023124698,0.0000046056475,0.000043750417,0.000018487975,0.00013935195,0.99480164,0.0015248233,0.000048514292,0.0028132773],"study_design_scores_gemma":[0.000012719517,0.000097438075,0.009362003,0.000006028162,0.000009061839,0.0001503816,0.00004493902,0.0016098449,0.9851232,0.0014028226,0.0021702533,0.000011400908],"about_ca_topic_score_codex":0.00064708147,"about_ca_topic_score_gemma":0.0014031543,"teacher_disagreement_score":0.0009969173,"about_ca_system_score_codex":0.00046651973,"about_ca_system_score_gemma":0.0002045469,"threshold_uncertainty_score":0.0033848882},"labels":[],"label_agreement":null},{"id":"W3129379232","doi":"10.1038/s41588-021-00791-5","title":"The NCI Genomic Data Commons","year":2021,"lang":"pl","type":"article","venue":"Nature Genetics","topic":"Cancer Genomics and Diagnostics","field":"Biochemistry, Genetics and Molecular Biology","cited_by":211,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Terahertz Technology Solutions (Canada); Centre Hospitalier Universitaire Sainte-Justine; Ontario Institute for Cancer Research","funders":"National Cancer Institute","keywords":"Biology; Petabyte; Genomics; Commons; Interface (matter); Cancer; Computational biology; Genetics; Big data; Genome; Data mining; Gene; Computer science","score_opus":0.013594174502380202,"score_gpt":0.275273594384021,"score_spread":0.2616794198816408,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W3129379232","genre_codex":"dataset","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":null,"domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.0012698666,0.0034322627,0.021024426,0.09496287,0.012114326,0.00037758186,0.40490282,0.077238664,0.38467723],"genre_scores_gemma":[0.02617862,0.008889737,0.021211505,0.039770868,0.007555573,0.0016782196,0.59019905,0.03498913,0.26952732],"study_design_codex":"not_applicable","study_design_gemma":"not_applicable","domain_scores_codex":[0.9907873,0.0015258096,0.0007738218,0.00069005584,0.005568309,0.00065459963],"domain_scores_gemma":[0.926535,0.02165414,0.0024658104,0.030186987,0.010019368,0.009138682],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.012484384,0.001447817,0.002129819,0.0074251215,0.0024947831,0.012122677,0.0068140924,0.0041346177,0.29103833],"category_scores_gemma":[0.09677826,0.001573405,0.0010063977,0.014430753,0.0034379046,0.009446342,0.012631341,0.006575017,0.2563675],"study_design_candidate":"not_applicable","study_design_consensus":"not_applicable","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0000310492,0.000017238195,0.00017438275,0.000110326066,0.0000045783604,0.000037707698,0.0000639611,0.00012569639,0.00015555724,0.006741757,0.96820486,0.024332993],"study_design_scores_gemma":[0.000019522808,0.0000045093248,0.00031202342,0.00009319791,0.0000039564275,0.000046529967,0.000053905434,0.0002943436,0.00017644008,0.011131307,0.98784584,0.000018329472],"about_ca_topic_score_codex":0.024961762,"about_ca_topic_score_gemma":0.01365376,"teacher_disagreement_score":0.29103833,"about_ca_system_score_codex":0.0045737927,"about_ca_system_score_gemma":0.0146096,"threshold_uncertainty_score":0.97362024},"labels":[],"label_agreement":null},{"id":"W3132166484","doi":"10.1038/s41588-026-02585-z","title":"Transposable Elements Shape Stemness in Normal and Leukemic Hematopoiesis","year":2021,"lang":"en","type":"preprint","venue":"Nature Genetics","topic":"Acute Myeloid Leukemia Research","field":"Medicine","cited_by":3,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Ontario Institute for Cancer Research; University of Toronto; Princess Margaret Cancer Centre; University Health Network","funders":"CIHR Skin Research Training Centre; Japan Society for the Promotion of Science; Canadian Cancer Society Research Institute; Canadian Institutes of Health Research; Terry Fox Research Institute; Ontario Institute for Cancer Research; Princess Margaret Cancer Foundation","keywords":"Chromatin; Haematopoiesis; Biology; Stem cell; Myeloid leukemia; Leukemia; Cancer research; Hematopoietic stem cell; Myeloid; Cancer stem cell; Genetics; Computational biology; Gene","score_opus":0.016303144616169298,"score_gpt":0.3035756961441592,"score_spread":0.2872725515279899,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W3132166484","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.98473006,0.0010541095,0.008486438,0.00016539192,0.000033181444,0.000016021095,0.000434877,0.0002784272,0.0048014564],"genre_scores_gemma":[0.9934,0.00031368024,0.0032418785,0.00004271842,0.000008897219,0.0000051957386,0.00031058386,0.00003164483,0.002645394],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9999492,0.0000054521083,0.0000020898583,0.0000143387715,0.000020869835,0.000008034443],"domain_scores_gemma":[0.9999591,0.00001028596,0.000010255644,0.000003987997,0.0000046554833,0.000011743452],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00010135266,0.00015483657,0.00009927231,0.00020009397,0.00009686818,0.00041445516,0.00008942964,0.00022998359,0.0017547548],"category_scores_gemma":[0.0001505153,0.00009171483,0.000074089236,0.00011475859,0.00027633514,0.00019284045,0.00023773045,0.00020497601,0.0005155219],"study_design_candidate":"bench_or_experimental","study_design_consensus":"bench_or_experimental","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00007982472,0.000008319687,0.0016652878,0.000027105378,0.0000032918922,0.0000738608,0.00003740778,0.00033654866,0.9908755,0.0017817012,0.00016477563,0.0049462942],"study_design_scores_gemma":[0.00004610418,0.00028624813,0.053803466,0.00001739994,0.000021820793,0.0008449951,0.00020424949,0.014483223,0.9109584,0.0067276303,0.012587755,0.000018603308],"about_ca_topic_score_codex":0.0003174519,"about_ca_topic_score_gemma":0.00038318036,"teacher_disagreement_score":0.0017547548,"about_ca_system_score_codex":0.00024311531,"about_ca_system_score_gemma":0.00008554222,"threshold_uncertainty_score":0.0058702826},"labels":[],"label_agreement":null},{"id":"W3134184401","doi":"10.1038/s41588-021-00783-5","title":"The Polygenic Score Catalog as an open database for reproducibility and systematic evaluation","year":2021,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Genetic Associations and Epidemiology","field":"Biochemistry, Genetics and Molecular Biology","cited_by":744,"is_retracted":false,"has_abstract":false,"route_ca_aff":false,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"","funders":"Health Data Research UK; National Human Genome Research Institute; Medical Research Council; Engineering and Physical Sciences Research Council; Canadian Institutes of Health Research; National Institute for Health and Care Research; Baker IDI Heart and Diabetes Institute; European Bioinformatics Institute; Wellcome Trust; British Heart Foundation; Government of Canada","keywords":"Biology; Metadata; Resource (disambiguation); Computational biology; Bioinformatics; Computer science; World Wide Web; Information retrieval; Database","score_opus":0.03726199298882381,"score_gpt":0.3643421259135172,"score_spread":0.3270801329246934,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W3134184401","genre_codex":"dataset","genre_gemma":"methods","domain_codex":null,"domain_gemma":"reproducibility","model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"methods","genre_consensus":null,"domain_candidate":"reproducibility","domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.013469129,0.002859141,0.23773064,0.0024849128,0.0012115489,0.0017947931,0.62889147,0.09524836,0.016309995],"genre_scores_gemma":[0.03498307,0.0016230117,0.22844428,0.0013099324,0.0005124146,0.0034949845,0.7120816,0.01336272,0.00418794],"study_design_codex":"not_applicable","study_design_gemma":"not_applicable","domain_scores_codex":[0.97330654,0.0065965005,0.008661466,0.003806996,0.006848053,0.0007804498],"domain_scores_gemma":[0.76403815,0.07802505,0.0167111,0.10059272,0.031462748,0.009170249],"candidate_categories":["metaresearch","open_science"],"consensus_categories":[],"category_scores_codex":[0.040871654,0.0017367475,0.0037999048,0.02738717,0.0019568335,0.008521655,0.0065225083,0.0022969674,0.034676854],"category_scores_gemma":[0.17894027,0.0017381551,0.0022322065,0.025314387,0.0011283467,0.005537472,0.010530264,0.0033154704,0.022825832],"study_design_candidate":"not_applicable","study_design_consensus":"not_applicable","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0017526571,0.0006602383,0.03614425,0.0048519545,0.002473219,0.0005390605,0.0009782634,0.0021376184,0.003844315,0.04990031,0.59397215,0.30274597],"study_design_scores_gemma":[0.0012207621,0.00031480327,0.06274535,0.0025277946,0.0018067661,0.0013363836,0.00044304712,0.012173785,0.0071379403,0.1015978,0.80809796,0.0005976164],"about_ca_topic_score_codex":0.0062835505,"about_ca_topic_score_gemma":0.007534715,"teacher_disagreement_score":0.99347746,"about_ca_system_score_codex":0.0014152061,"about_ca_system_score_gemma":0.012762671,"threshold_uncertainty_score":0.21615255},"labels":[],"label_agreement":null},{"id":"W3134771351","doi":"10.1038/s41588-021-00787-1","title":"Identifying loci with different allele frequencies among cases of eight psychiatric disorders using CC-GWAS","year":2021,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Genetic Associations and Epidemiology","field":"Biochemistry, Genetics and Molecular Biology","cited_by":117,"is_retracted":false,"has_abstract":false,"route_ca_aff":false,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"","funders":"National Cancer Institute; National Institute of Mental Health; Cancer Research UK; Horizon 2020 Framework Programme; National Human Genome Research Institute; Nederlandse Organisatie voor Wetenschappelijk Onderzoek; ZonMw; European Commission; National Institutes of Health; U.S. Department of Health and Human Services; Government of Canada; Canadian Institutes of Health Research; Genome Canada","keywords":"Genome-wide association study; Biology; Genetic association; Schizophrenia (object-oriented programming); Bipolar disorder; Genetics; Single-nucleotide polymorphism; Medicine; Psychiatry; Gene; Genotype; Neuroscience","score_opus":0.01285643926570782,"score_gpt":0.27174096373345247,"score_spread":0.2588845244677446,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W3134771351","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9974241,0.00027162716,0.0012827658,0.0000772176,0.00002215594,0.000019136882,0.00042925164,0.00002990309,0.0004438833],"genre_scores_gemma":[0.9987319,0.00005203844,0.0007439675,0.000030424873,0.000011763228,0.000010623249,0.00023767303,0.000014346086,0.0001672489],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9971232,0.0008513214,0.0003399351,0.0009466161,0.00035882686,0.00038009742],"domain_scores_gemma":[0.99581474,0.0018501837,0.00095488806,0.0006078907,0.0003455171,0.0004267149],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0016535902,0.0008950087,0.0006936378,0.0035858117,0.0010967442,0.0014279105,0.0009064172,0.0011663234,0.0033939355],"category_scores_gemma":[0.006230409,0.00045162588,0.0018142711,0.004423138,0.00070943136,0.00046955756,0.0011557438,0.0009464104,0.00029157236],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0009632332,0.000044503147,0.98093545,0.000041904434,0.0011518386,0.0006510648,0.00028171955,0.00018793649,0.010444104,0.0002789903,0.0001895773,0.0048297],"study_design_scores_gemma":[0.00009530265,0.0001513163,0.99229795,0.000022762657,0.0011093819,0.0016762754,0.00037912355,0.0012833194,0.0017356384,0.00049655314,0.000720976,0.000031322576],"about_ca_topic_score_codex":0.01034879,"about_ca_topic_score_gemma":0.01240621,"teacher_disagreement_score":0.01034879,"about_ca_system_score_codex":0.00039050129,"about_ca_system_score_gemma":0.0006433268,"threshold_uncertainty_score":0.020577133},"labels":[],"label_agreement":null},{"id":"W3137944384","doi":"10.1038/s41588-021-00807-0","title":"Chromosome-scale genome assembly provides insights into rye biology, evolution and agronomic potential","year":2021,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Wheat and Barley Genetics and Pathology","field":"Agricultural and Biological Sciences","cited_by":272,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Agriculture and Agri-Food Canada; Saskatchewan Research Council (Canada); University of Saskatchewan","funders":"Leibniz-Gemeinschaft; Agriculture and Agri-Food Canada; Directorate for Biological Sciences; European Regional Development Fund; German Network for Bioinformatics Infrastructure; Grantová Agentura České Republiky; Bundesministerium für Ernährung und Landwirtschaft; Deutsche Forschungsgemeinschaft; Universitätsmedizin Göttingen; Biotechnology and Biological Sciences Research Council; Noble Research Institute; Bundesministerium für Bildung und Forschung; Montana Wheat and Barley Committee","keywords":"Biology; Secale; Domestication; Genome; Germplasm; Introgression; Gene pool; Plant disease resistance; Genetics; Chromosome; Biotechnology; Gene; Agronomy; Genetic diversity","score_opus":0.006950676464215408,"score_gpt":0.21407286023907596,"score_spread":0.20712218377486055,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W3137944384","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.70581377,0.004203978,0.19680712,0.0007936278,0.00019966255,0.00017481571,0.07871531,0.0036627678,0.009628895],"genre_scores_gemma":[0.6195577,0.0038403994,0.18244208,0.00021712529,0.000059393806,0.00013878656,0.18758886,0.0015827755,0.0045729973],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99984455,0.000017701768,0.00001242021,0.00007753649,0.00002940698,0.000018324083],"domain_scores_gemma":[0.999569,0.00010767885,0.000058323683,0.00011556518,0.00009476244,0.00005476527],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00035325062,0.0006114586,0.000467726,0.0011925692,0.00041744727,0.0010260014,0.0003303914,0.00044464014,0.002273069],"category_scores_gemma":[0.00078945543,0.00034179908,0.0007184257,0.001074515,0.00021391307,0.00064481725,0.00066557893,0.0009965426,0.0019500785],"study_design_candidate":"bench_or_experimental","study_design_consensus":"bench_or_experimental","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00023157193,0.00004517404,0.007926609,0.00030187125,0.00013608414,0.00037155487,0.00030541327,0.0020621778,0.9651626,0.0015104231,0.0012280053,0.020718468],"study_design_scores_gemma":[0.00013690452,0.0005931432,0.39945623,0.00035739518,0.00091146294,0.002297632,0.0009053044,0.031143403,0.34079096,0.009083464,0.21410407,0.00022009976],"about_ca_topic_score_codex":0.0026327616,"about_ca_topic_score_gemma":0.007089678,"teacher_disagreement_score":0.0026327616,"about_ca_system_score_codex":0.0003312145,"about_ca_system_score_gemma":0.000529266,"threshold_uncertainty_score":0.0076042414},"labels":[],"label_agreement":null},{"id":"W3138494859","doi":"10.1038/s41588-021-00832-z","title":"Publisher Correction: Discovery of rare variants associated with blood pressure regulation through meta-analysis of 1.3 million individuals","year":2021,"lang":"en","type":"erratum","venue":"Nature Genetics","topic":"Nutrition, Genetics, and Disease","field":"Biochemistry, Genetics and Molecular Biology","cited_by":3,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Université Laval; Population Health Research Institute; McMaster University","funders":"Novo Nordisk Fonden; Medical Research Council; U.S. Department of Veterans Affairs; National Institute for Health and Care Research; Steno Diabetes Center Aarhus; Wellcome Trust","keywords":"Biology; Meta-analysis; Computational biology; Genetics; Evolutionary biology; Internal medicine; Medicine","score_opus":0.015275036735366853,"score_gpt":0.2549819964200274,"score_spread":0.23970695968466055,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W3138494859","genre_codex":"editorial","genre_gemma":"other","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"other","genre_consensus":null,"domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.00024207398,0.00087313214,0.0014417202,0.03858826,0.9484511,0.00003938614,0.0063314843,0.00071080617,0.0033220067],"genre_scores_gemma":[0.030233478,0.008490092,0.018682878,0.10258652,0.3466746,0.00084317767,0.022594683,0.007967442,0.4619271],"study_design_codex":"not_applicable","study_design_gemma":"not_applicable","domain_scores_codex":[0.9936784,0.0012243642,0.0013401448,0.0009366806,0.0023796977,0.00044086005],"domain_scores_gemma":[0.9568062,0.014090337,0.002130191,0.0038152873,0.021588117,0.0015698562],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00707123,0.0028513058,0.0027752444,0.0052950243,0.0032616481,0.0044079907,0.005482261,0.005624502,0.13225347],"category_scores_gemma":[0.10519402,0.0018535163,0.0024808685,0.0043436955,0.0020849959,0.0023884678,0.0024703247,0.01056352,0.0511131],"study_design_candidate":"not_applicable","study_design_consensus":"not_applicable","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00003709878,0.0000035761946,0.000119829565,0.00015691835,0.000034207522,0.00028906576,0.000023055441,0.000048525308,0.00003385384,0.00044196134,0.99517834,0.0036336863],"study_design_scores_gemma":[0.00025698481,0.00003330015,0.002193686,0.0011671508,0.00025625087,0.0022577385,0.000120074306,0.00055649446,0.00063253933,0.004151369,0.98826236,0.000111941525],"about_ca_topic_score_codex":0.021513406,"about_ca_topic_score_gemma":0.028426686,"teacher_disagreement_score":0.13225347,"about_ca_system_score_codex":0.003454216,"about_ca_system_score_gemma":0.0061527006,"threshold_uncertainty_score":0.44243193},"labels":[],"label_agreement":null},{"id":"W3144460008","doi":"10.1038/s41588-021-00825-y","title":"A resource of targeted mutant mouse lines for 5,061 genes","year":2021,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Molecular Biology Techniques and Applications","field":"Biochemistry, Genetics and Molecular Biology","cited_by":114,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Hospital for Sick Children; Toronto Centre for Phenogenomics","funders":"National Human Genome Research Institute; Medical Research Council; National Cancer Institute; National Institutes of Health; Agence Nationale de la Recherche; Wellcome Trust","keywords":"Mutant; Biology; Gene; Genetics; Allele; Null allele; Reporter gene; Computational biology; Gene targeting; Gene expression","score_opus":0.006735047348694573,"score_gpt":0.2744391762920666,"score_spread":0.26770412894337203,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W3144460008","genre_codex":"dataset","genre_gemma":"dataset","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"dataset","genre_consensus":"dataset","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.07989651,0.008929055,0.24680646,0.0013893746,0.0007618802,0.0027024758,0.5541717,0.052187182,0.053155374],"genre_scores_gemma":[0.03763418,0.0074378345,0.20811637,0.0007482382,0.00015373252,0.0043158443,0.655761,0.010475981,0.075356916],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99921346,0.00007728659,0.00012137466,0.00012680677,0.00034603968,0.00011501093],"domain_scores_gemma":[0.9983304,0.00032617006,0.00026373984,0.00046551757,0.00027104685,0.00034312907],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0012998179,0.002062129,0.0013793245,0.009397032,0.0013363588,0.0009009148,0.004758735,0.0012969855,0.05308688],"category_scores_gemma":[0.0010457275,0.0019407314,0.0013965713,0.00416225,0.00039229245,0.0009319618,0.0013662447,0.0021229237,0.039135408],"study_design_candidate":"bench_or_experimental","study_design_consensus":"bench_or_experimental","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00093913905,0.00048085657,0.0010704786,0.00076954265,0.00013996767,0.00056584046,0.000108580716,0.0007921376,0.82866615,0.0036517452,0.093459055,0.069356464],"study_design_scores_gemma":[0.0008329274,0.0006528981,0.008461139,0.00032296177,0.0005541037,0.0043662675,0.000051224248,0.002268438,0.43078655,0.0029376168,0.54852825,0.00023766405],"about_ca_topic_score_codex":0.002530714,"about_ca_topic_score_gemma":0.009023327,"teacher_disagreement_score":0.05308688,"about_ca_system_score_codex":0.00064723566,"about_ca_system_score_gemma":0.0012680818,"threshold_uncertainty_score":0.17759329},"labels":[],"label_agreement":null},{"id":"W3150131477","doi":"10.1038/s41588-021-00803-4","title":"Gain-of-function variants in SYK cause immune dysregulation and systemic inflammation in humans and mice","year":2021,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Mast cells and histamine","field":"Immunology and Microbiology","cited_by":108,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Ontario Institute for Cancer Research; Université de Montréal; Princess Margaret Cancer Centre; St. Michael's Hospital; Hospital for Sick Children; Centre Hospitalier Universitaire Sainte-Justine; McMaster University; University Health Network; University of Toronto; SickKids Foundation","funders":"National Institute of Diabetes and Digestive and Kidney Diseases; National Institute for Health and Care Research; Cancer Research UK; Wellcome Trust","keywords":"Syk; Inflammation; Biology; Immune system; Immunology; Cancer research; Immune dysregulation; Spleen; Signal transduction; Tyrosine kinase; Cell biology","score_opus":0.005990995914436157,"score_gpt":0.2140283636235222,"score_spread":0.20803736770908604,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W3150131477","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.98870313,0.001576067,0.004595951,0.00078018964,0.00020595985,0.00005890587,0.0018326076,0.00028654258,0.0019607728],"genre_scores_gemma":[0.99446493,0.0010591985,0.0019136234,0.00032623293,0.00011098267,0.000043012773,0.00067756063,0.0001427166,0.0012618976],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99942446,0.00009453862,0.0000770127,0.00022862696,0.00010136653,0.0000740292],"domain_scores_gemma":[0.99960893,0.000100689555,0.00017364527,0.000035391564,0.000015425876,0.00006607281],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00033284852,0.0018325277,0.0007495539,0.0012117496,0.00046518823,0.000674509,0.0004827211,0.0016393462,0.005438713],"category_scores_gemma":[0.0006254334,0.0004356939,0.0009851707,0.0005802468,0.0015677849,0.00032350433,0.0007842021,0.0012069598,0.00056219875],"study_design_candidate":"bench_or_experimental","study_design_consensus":"bench_or_experimental","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0038370262,0.00021907027,0.01303259,0.00024139107,0.0005375608,0.01402919,0.0002462169,0.00067376916,0.95164835,0.0023821152,0.0015358274,0.011616861],"study_design_scores_gemma":[0.0030779848,0.0051252237,0.5054203,0.0005753299,0.0041150646,0.1744928,0.0016725826,0.0091466475,0.25523856,0.008731638,0.03198663,0.00041731226],"about_ca_topic_score_codex":0.0010135479,"about_ca_topic_score_gemma":0.0010275729,"teacher_disagreement_score":0.005438713,"about_ca_system_score_codex":0.00030331445,"about_ca_system_score_gemma":0.00028508028,"threshold_uncertainty_score":0.018194318},"labels":[],"label_agreement":null},{"id":"W3161789746","doi":"10.1038/s41588-021-00883-2","title":"Author Correction: The NCI Genomic Data Commons","year":2021,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Genomics and Rare Diseases","field":"Biochemistry, Genetics and Molecular Biology","cited_by":1,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Université de Montréal; Terahertz Technology Solutions (Canada); Centre Hospitalier Universitaire Sainte-Justine; Ontario Institute for Cancer Research","funders":"","keywords":"Biology; Computational biology; Commons; Genetics","score_opus":0.01671162310135811,"score_gpt":0.28292326247274663,"score_spread":0.26621163937138853,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W3161789746","genre_codex":"editorial","genre_gemma":"editorial","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"editorial","genre_consensus":"editorial","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.0003195777,0.0009237785,0.0017293434,0.10873092,0.86041415,0.00006298622,0.019492341,0.0017487523,0.006578063],"genre_scores_gemma":[0.039739743,0.0076066377,0.011389998,0.19571652,0.3745549,0.0012647032,0.055855595,0.010866285,0.30300558],"study_design_codex":"not_applicable","study_design_gemma":"not_applicable","domain_scores_codex":[0.9802782,0.0030560654,0.0026325968,0.0019961277,0.010280478,0.0017565279],"domain_scores_gemma":[0.84560776,0.040223084,0.008317291,0.021519944,0.077779345,0.0065525463],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.013973899,0.001607557,0.002710312,0.009274141,0.0043331436,0.009307709,0.007323867,0.007882682,0.21790686],"category_scores_gemma":[0.21553056,0.0015835614,0.0018124862,0.008713971,0.0029322223,0.0041346434,0.006987022,0.013559408,0.072702855],"study_design_candidate":"not_applicable","study_design_consensus":"not_applicable","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.000022228543,0.0000033557744,0.00008887432,0.00006636584,0.000010619912,0.00007659933,0.00002187618,0.000022620103,0.000016203736,0.00062220066,0.9957575,0.003291499],"study_design_scores_gemma":[0.000052498854,0.0000068190516,0.0005252803,0.00038754335,0.000031596384,0.00033315626,0.00011093411,0.00021274005,0.0002052166,0.0033267688,0.9947733,0.000034097735],"about_ca_topic_score_codex":0.01706052,"about_ca_topic_score_gemma":0.017492365,"teacher_disagreement_score":0.21790686,"about_ca_system_score_codex":0.004889738,"about_ca_system_score_gemma":0.011447253,"threshold_uncertainty_score":0.72897106},"labels":[],"label_agreement":null},{"id":"W3162084837","doi":"10.1038/s41588-021-00856-5","title":"Two competing mechanisms of DNMT3A recruitment regulate the dynamics of de novo DNA methylation at PRC1-targeted CpG islands","year":2021,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Epigenetics and DNA Methylation","field":"Biochemistry, Genetics and Molecular Biology","cited_by":107,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"McGill Genome Centre; McGill University","funders":"National Institute of General Medical Sciences; McGill University; Damon Runyon Cancer Research Foundation; American Association for Cancer Research; St. Jude Children's Research Hospital; National Cancer Institute; National Institutes of Health; U.S. Department of Health and Human Services","keywords":"Biology; DNA methylation; EZH2; Histone; Histone H3; Epigenetics; CpG site; Histone methylation; Genetics; Epigenomics; Methylation; Cell biology; Cancer epigenetics; Histone methyltransferase; DNA; Gene; Gene expression","score_opus":0.014012670405292653,"score_gpt":0.28661900342723395,"score_spread":0.2726063330219413,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W3162084837","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.91881144,0.008297397,0.05892745,0.0015714286,0.00044827032,0.00021088558,0.0011732939,0.0009337972,0.009625924],"genre_scores_gemma":[0.9775973,0.001032731,0.013610564,0.00017867362,0.000051019586,0.00018609565,0.0005744128,0.00019327186,0.006575964],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99830073,0.000120628945,0.00013926676,0.0005959269,0.0004223039,0.00042117172],"domain_scores_gemma":[0.9982839,0.00059704523,0.00023892103,0.00022993382,0.00025658755,0.00039353644],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0018643183,0.0006152062,0.001372485,0.000751606,0.0010352427,0.0031629512,0.0015712798,0.0014246255,0.0048481557],"category_scores_gemma":[0.0031174896,0.0012490496,0.0010565545,0.00044908017,0.0011623518,0.0032059618,0.0022009904,0.0021237996,0.0018739242],"study_design_candidate":"bench_or_experimental","study_design_consensus":"bench_or_experimental","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00085884135,0.00007210191,0.0039240574,0.0003159302,0.000066226734,0.00012590227,0.00030202008,0.00074435305,0.9682593,0.014464863,0.0005646079,0.010301743],"study_design_scores_gemma":[0.00013318621,0.00011663297,0.020004675,0.000025845116,0.000046552454,0.00030902348,0.00017092658,0.0175035,0.95545965,0.0022008452,0.003942015,0.00008714986],"about_ca_topic_score_codex":0.0022651323,"about_ca_topic_score_gemma":0.004638835,"teacher_disagreement_score":0.0048481557,"about_ca_system_score_codex":0.002613014,"about_ca_system_score_gemma":0.0012920925,"threshold_uncertainty_score":0.018958807},"labels":[],"label_agreement":null},{"id":"W3162259891","doi":"10.1038/s41588-021-00857-4","title":"Genome-wide association study of more than 40,000 bipolar disorder cases provides new insights into the underlying biology","year":2021,"lang":"en","type":"review","venue":"Nature Genetics","topic":"Genetic Associations and Epidemiology","field":"Biochemistry, Genetics and Molecular Biology","cited_by":1593,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Public Health Ontario; McGill University; Dalhousie University; Montreal Neurological Institute and Hospital; University of Toronto; Centre for Addiction and Mental Health; McGill University Health Centre","funders":"National Institute of Mental Health; Medical Research Council; Institute of Psychiatry, Psychology and Neuroscience, King’s College London; School of Medicine, Emory University; National Institutes of Health; Université de Paris; Assistance publique-Hôpitaux de Paris; University of Cape Town; Centre d'Imagerie BioMédicale; Universitat de Barcelona; Háskóli Íslands; Universitetet i Oslo; Umeå Universitet; University of California, Irvine; Universidad Autónoma de Madrid; McDonnell Center for Systems Neuroscience; University of Melbourne; University of Toronto; University of Glasgow; University of New South Wales; South African Medical Research Council; Universidad de Granada; Karolinska Institutet; School of Medicine, University of California, Irvine; Lundbeckfonden; Institut National de la Santé et de la Recherche Médicale; Emory University; Westfälische Wilhelms-Universität Münster; University of Oxford; Neuroscience Research Australia; Vanderbilt University; King's College London; Diakonhjemmet; Centro de Biología Molecular Severo Ochoa; Vanderbilt University Medical Center; Pfizer; National Institute for Health and Care Research; Agence Nationale de la Recherche; University of Southern California; World Health Organization; U.S. Department of Health and Human Services","keywords":"Biology; Genome-wide association study; Computational biology; Bipolar disorder; Genetics; Genetic association; Genome; Association (psychology); Evolutionary biology; Single-nucleotide polymorphism; Gene; Genotype; Neuroscience","score_opus":0.03286501014639599,"score_gpt":0.34297914082394715,"score_spread":0.31011413067755117,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W3162259891","genre_codex":"review","genre_gemma":"review","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"review","genre_consensus":"review","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.00005834682,0.9985532,0.00012653315,0.0004487979,0.00016799885,0.0000034894097,0.00003462511,0.00000837386,0.00059864693],"genre_scores_gemma":[0.00041270445,0.99845314,0.00016603053,0.00036563468,0.00018258777,0.000005594202,0.0000716821,0.000002362859,0.0003402074],"study_design_codex":"design_other","study_design_gemma":"observational","domain_scores_codex":[0.99962056,0.000086647495,0.000056173387,0.00008945375,0.00011642794,0.000030782267],"domain_scores_gemma":[0.9985613,0.0008232832,0.00012541124,0.000040566167,0.0003197267,0.00012965992],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0017848307,0.0013048074,0.0022323022,0.0029197535,0.00023362225,0.0009896174,0.0011818154,0.0014758783,0.0028651922],"category_scores_gemma":[0.0018771064,0.0003724477,0.00062237907,0.0029955264,0.0006247158,0.0009938201,0.00078952167,0.0020298113,0.002263399],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00010358363,0.000028345263,0.00045812054,0.008993009,0.00026824718,0.00017237083,0.000025130048,0.00018787384,0.0005212908,0.001994602,0.037151728,0.9500957],"study_design_scores_gemma":[0.00004413889,0.00012301773,0.0034958788,0.005903939,0.00046632768,0.0015330025,0.00005150192,0.00007650476,0.00028794748,0.0027445448,0.98524076,0.00003236781],"about_ca_topic_score_codex":0.00193546,"about_ca_topic_score_gemma":0.0034571767,"teacher_disagreement_score":0.0029197535,"about_ca_system_score_codex":0.0009960505,"about_ca_system_score_gemma":0.0016783088,"threshold_uncertainty_score":0.009585023},"labels":[],"label_agreement":null},{"id":"W3174213828","doi":"10.1038/s41588-021-00886-z","title":"Pathogenic SPTBN1 variants cause an autosomal dominant neurodevelopmental syndrome","year":2021,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Erythrocyte Function and Pathophysiology","field":"Medicine","cited_by":108,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"SickKids Foundation; Hospital for Sick Children; University of Toronto; McMaster University","funders":"Common Fund; National Cancer Institute; National Institute of Mental Health; Howard Hughes Medical Institute; Medical Research Council; Intellectual and Developmental Disabilities Research Center; Department of Health and Social Care; National Institute of Neurological Disorders and Stroke; National Institute for Health and Care Research; Eunice Kennedy Shriver National Institute of Child Health and Human Development; University of North Carolina at Chapel Hill; National Ataxia Foundation; National Institutes of Health; U.S. Department of Health and Human Services; Cancer Research UK; National Human Genome Research Institute; Wellcome Trust","keywords":"Spectrin; Biology; Hypotonia; Haploinsufficiency; Phenotype; Neurodevelopmental disorder; Genetics; Neuroscience; Mutation; Gene; Cytoskeleton","score_opus":0.015031247235574221,"score_gpt":0.26799527177992594,"score_spread":0.25296402454435174,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W3174213828","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.98423094,0.0012344543,0.004762189,0.0017221145,0.00035950166,0.00004335088,0.0010255812,0.00021324524,0.0064086574],"genre_scores_gemma":[0.99518836,0.00032420375,0.0024743034,0.00020789883,0.00010239957,0.000013586241,0.00026824482,0.000053697997,0.0013674119],"study_design_codex":"case_report","study_design_gemma":"observational","domain_scores_codex":[0.999647,0.000039722498,0.000045611003,0.00008497415,0.00013588248,0.000046793917],"domain_scores_gemma":[0.9993887,0.00018427921,0.00019163414,0.000031402556,0.000072727235,0.00013130289],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00022675475,0.0017083797,0.0004814624,0.0010160882,0.0008248487,0.00048247984,0.00090687635,0.002235113,0.0030243923],"category_scores_gemma":[0.0015120425,0.00029495993,0.0004758627,0.0008159707,0.0009910166,0.000313294,0.0009884542,0.0010424952,0.00050252036],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0005631487,0.00008675549,0.035359863,0.00013976127,0.00019071755,0.7769197,0.00068679237,0.0010093658,0.16516504,0.002822815,0.003818136,0.013237948],"study_design_scores_gemma":[0.00019167454,0.00027491848,0.09257606,0.00015969345,0.00033736668,0.8468923,0.0005296201,0.004224359,0.041905764,0.002624383,0.010205772,0.00007810631],"about_ca_topic_score_codex":0.0027071587,"about_ca_topic_score_gemma":0.0026991447,"teacher_disagreement_score":0.0030243923,"about_ca_system_score_codex":0.00047777026,"about_ca_system_score_gemma":0.0004985242,"threshold_uncertainty_score":0.01011765},"labels":[],"label_agreement":null},{"id":"W3180961869","doi":"10.1038/s41588-021-00895-y","title":"Haplotype-resolved genome assembly provides insights into evolutionary history of the tea plant Camellia sinensis","year":2021,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Plant and Fungal Interactions Research","field":"Biochemistry, Genetics and Molecular Biology","cited_by":377,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Brock University","funders":"National Natural Science Foundation of China","keywords":"Biology; Camellia sinensis; Domestication; Genetic diversity; Genome; Selective sweep; Haplotype; Genetics; Population; Allele; Gene; Botany","score_opus":0.011736015569304287,"score_gpt":0.24876010709299204,"score_spread":0.23702409152368775,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W3180961869","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.90964264,0.0018800215,0.049229264,0.00036394008,0.000096201074,0.00007871931,0.031518146,0.0013512701,0.0058398615],"genre_scores_gemma":[0.8829397,0.00092286844,0.04919851,0.00014332178,0.000049314724,0.00006511667,0.06454098,0.0005964479,0.0015436659],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9998412,0.000022932807,0.000014868242,0.00007529482,0.00002614397,0.000019489957],"domain_scores_gemma":[0.9996184,0.000095765776,0.00007928654,0.000080907244,0.00006623286,0.00005936577],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00047407183,0.0003428269,0.00041561044,0.0014080422,0.0005138365,0.00072300347,0.00027583292,0.00037943808,0.0019758455],"category_scores_gemma":[0.0008786057,0.00023710208,0.00071233977,0.0011374414,0.00015542116,0.00046434382,0.0005939677,0.000662862,0.00094139494],"study_design_candidate":"bench_or_experimental","study_design_consensus":"bench_or_experimental","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00070437323,0.00010902084,0.060403343,0.00068758946,0.0004120855,0.0012778142,0.0012554146,0.004069715,0.8833326,0.0022604652,0.0019459566,0.04354168],"study_design_scores_gemma":[0.00016403054,0.00050986104,0.76408565,0.00028406552,0.0009848654,0.0024474182,0.0010992358,0.036065184,0.0835191,0.007759213,0.102918565,0.00016289487],"about_ca_topic_score_codex":0.0016603337,"about_ca_topic_score_gemma":0.005021448,"teacher_disagreement_score":0.0019758455,"about_ca_system_score_codex":0.00031770347,"about_ca_system_score_gemma":0.00039431205,"threshold_uncertainty_score":0.0066097975},"labels":[],"label_agreement":null},{"id":"W3196488607","doi":"10.1038/s41588-021-00920-0","title":"Genomic and evolutionary classification of lung cancer in never smokers","year":2021,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Cancer Genomics and Diagnostics","field":"Biochemistry, Genetics and Molecular Biology","cited_by":242,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Calgary; Université Laval; Institut universitaire de cardiologie et de pneumologie de Québec","funders":"National Institute of Environmental Health Sciences; National Cancer Institute; National Heart, Lung, and Blood Institute; Yale University; Moffitt Cancer Center; Institut universitaire de cardiologie et de pneumologie de Québec, Université Laval; Connaught Fund; Wellcome Trust; Division of Cancer Epidemiology and Genetics, National Cancer Institute; National Institute for Health and Care Research; Université Laval; Damon Runyon Cancer Research Foundation; National Institutes of Health; U.S. Department of Health and Human Services","keywords":"Biology; Lung cancer; KRAS; Genetics; Cancer; Germline; Genome; Somatic cell; Germline mutation; Gene; Cancer research; Bioinformatics; Mutation; Oncology; Medicine","score_opus":0.005884159671011902,"score_gpt":0.2605079997156475,"score_spread":0.25462384004463556,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W3196488607","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99787545,0.0004932001,0.00027844397,0.00012663213,0.0000074086265,0.000005004888,0.0002103634,0.0000046782384,0.0009988568],"genre_scores_gemma":[0.99896693,0.00020123507,0.0001461051,0.00004497932,0.000012011717,0.0000030996564,0.00029999728,0.000006306978,0.00031929518],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9993692,0.00017288259,0.000041217172,0.00015478618,0.00008969639,0.00017223174],"domain_scores_gemma":[0.9992021,0.00025399562,0.00018078047,0.0000687257,0.00013421044,0.00016014827],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.000563857,0.00018042617,0.0002687228,0.0030220512,0.0008117816,0.00079761643,0.00060416176,0.00070313603,0.0024902096],"category_scores_gemma":[0.0015370233,0.00014540889,0.00046555174,0.0013736966,0.0006215628,0.00039801552,0.00073695293,0.00060979876,0.00040099755],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00043103314,0.0000414201,0.9728497,0.000026695712,0.00011056932,0.00046073846,0.0005691499,0.0001826368,0.013531994,0.00061468215,0.00017568616,0.0110055525],"study_design_scores_gemma":[0.0000030254296,0.000049303464,0.9972197,0.0000087646295,0.000023356946,0.00094311126,0.00044763405,0.00029265805,0.00028401773,0.0003203259,0.00040373468,0.000004534796],"about_ca_topic_score_codex":0.0047449702,"about_ca_topic_score_gemma":0.0047966256,"teacher_disagreement_score":0.0047449702,"about_ca_system_score_codex":0.00034901162,"about_ca_system_score_gemma":0.00022770761,"threshold_uncertainty_score":0.0094347},"labels":[],"label_agreement":null},{"id":"W3197364483","doi":"10.1038/s41588-021-00913-z","title":"Large-scale cis- and trans-eQTL analyses identify thousands of genetic loci and polygenic scores that regulate blood gene expression","year":2021,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Single-cell and spatial transcriptomics","field":"Biochemistry, Genetics and Molecular Biology","cited_by":2182,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Ontario Institute for Cancer Research","funders":"Common Fund; National Institute of Environmental Health Sciences; National Institute of General Medical Sciences; National Heart, Lung, and Blood Institute; National Center for Advancing Translational Sciences; Medical Research Council; National Institute of Mental Health; Horizon 2020 Framework Programme; Freistaat Sachsen; Novo Nordisk Fonden; Universität Leipzig; Novo Nordisk; Jacobs Foundation; Nederlandse Organisatie voor Wetenschappelijk Onderzoek; Diabetes UK; Fonds Wetenschappelijk Onderzoek; National Human Genome Research Institute; University of Exeter; Fonds De La Recherche Scientifique - FNRS; Eesti Teadusagentuur; Academy of Finland; Koninklijke Nederlandse Akademie van Wetenschappen; Schweizerischer Nationalfonds zur Förderung der Wissenschaftlichen Forschung; National Cancer Institute; University of Bristol; ZonMw; European Regional Development Fund; Bundesministerium für Bildung und Forschung; National Institute on Aging; NHS Blood and Transplant; National Institute for Health and Care Research; National Institutes of Health; Rosetrees Trust; European Commission; Broad Institute; Universitair Medisch Centrum Groningen; Stichting de Drie Lichten; International Society on Thrombosis and Haemostasis; Leidos; British Heart Foundation; Wellcome Trust; Research England; University of Miami; National Science Foundation","keywords":"Expression quantitative trait loci; Biology; Quantitative trait locus; Genetics; Gene; Phenotype; Transcriptome; Gene expression; Regulation of gene expression; Locus (genetics); Computational biology; Single-nucleotide polymorphism; Genotype","score_opus":0.014241602268773936,"score_gpt":0.27691478581452883,"score_spread":0.2626731835457549,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W3197364483","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9084794,0.0010802387,0.0789596,0.00025594924,0.00005561059,0.00002876432,0.008216006,0.0007696913,0.002154713],"genre_scores_gemma":[0.96795815,0.00052914093,0.022517517,0.0003189,0.000031264382,0.000051507966,0.0053825113,0.00031571902,0.0028951967],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9996081,0.000038424478,0.000020619951,0.00018240891,0.00009598295,0.000054553635],"domain_scores_gemma":[0.99926263,0.00043074848,0.00012589383,0.000085771935,0.000041872925,0.000053038097],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0004450881,0.00052358053,0.0004994298,0.0010720703,0.00026609097,0.00054704637,0.00044531986,0.00034304726,0.0026568044],"category_scores_gemma":[0.00058286556,0.0003564726,0.0007059618,0.0011632274,0.00041116943,0.0003260986,0.0008085311,0.00085392967,0.00050989713],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00019940037,0.000028622815,0.017924633,0.000086243046,0.00018639126,0.0002275168,0.00013451479,0.0014226271,0.96045804,0.0015323693,0.00027507095,0.017524514],"study_design_scores_gemma":[0.00013619661,0.00024894116,0.6480149,0.000039761962,0.00078196224,0.0011610334,0.0002477111,0.035086207,0.29861873,0.007535388,0.007999675,0.00012945393],"about_ca_topic_score_codex":0.00196136,"about_ca_topic_score_gemma":0.0059198258,"teacher_disagreement_score":0.0026568044,"about_ca_system_score_codex":0.00031180173,"about_ca_system_score_gemma":0.00023269503,"threshold_uncertainty_score":0.008887947},"labels":[],"label_agreement":null},{"id":"W3202738945","doi":"10.1038/s41588-021-00926-8","title":"Single-cell multimodal glioma analyses identify epigenetic regulators of cellular plasticity and environmental stress response","year":2021,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Epigenetics and DNA Methylation","field":"Biochemistry, Genetics and Molecular Biology","cited_by":267,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Hospital for Sick Children; University of Toronto; St. Michael's Hospital","funders":"National Institute of Neurological Disorders and Stroke; U.S. Department of Health and Human Services; National Cancer Institute; American Brain Tumor Association; American Cancer Society; U.S. Department of Defense","keywords":"Epigenetics; DNA methylation; Biology; DNA damage; Transcriptome; Glioma; Methylation; Epigenomics; Genetics; Cell; Histone; Cancer research; DNA; Gene expression; Gene","score_opus":0.012097164004876192,"score_gpt":0.2736730986030842,"score_spread":0.261575934598208,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W3202738945","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9720058,0.0010631132,0.023068044,0.00018031511,0.000024823197,0.000027870505,0.0011429571,0.00027811812,0.0022089444],"genre_scores_gemma":[0.99027,0.0003819908,0.0059520574,0.000076742974,0.000008773634,0.000035770816,0.00047227342,0.00006576305,0.0027365994],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9998882,0.0000066897983,0.0000048321526,0.000036032612,0.000031357667,0.00003285516],"domain_scores_gemma":[0.99990857,0.000023614259,0.000017960583,0.000013370487,0.000018704912,0.000017765411],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00015024457,0.0002510326,0.00035933938,0.00034461558,0.00020964949,0.0005449735,0.00030776096,0.00042016528,0.0016622151],"category_scores_gemma":[0.00013781682,0.00017457845,0.00030803427,0.0002589414,0.00030429923,0.00037261567,0.00047413784,0.0007282753,0.00040625155],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.000034990808,0.0000044865096,0.0005051417,0.000015579926,0.000006463605,0.000021441061,0.000017468936,0.00013483374,0.9975259,0.00014301846,0.0000501138,0.0015407582],"study_design_scores_gemma":[0.000007291028,0.000060463677,0.022792865,0.0000025458612,0.000028293336,0.00015663341,0.000093897674,0.005384688,0.9695171,0.0002832051,0.0016624122,0.000010644196],"about_ca_topic_score_codex":0.0022945101,"about_ca_topic_score_gemma":0.009669608,"teacher_disagreement_score":0.0022945101,"about_ca_system_score_codex":0.00044384628,"about_ca_system_score_gemma":0.00017379767,"threshold_uncertainty_score":0.005560696},"labels":[],"label_agreement":null},{"id":"W3203889005","doi":"10.1038/s41588-021-00935-7","title":"A high-resolution HLA reference panel capturing global population diversity enables multi-ancestry fine-mapping in HIV host response","year":2021,"lang":"en","type":"article","venue":"Nature Genetics","topic":"T-cell and B-cell Immunology","field":"Immunology and Microbiology","cited_by":187,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Manitoba; Public Health Agency of Canada; University of Ottawa; McGill University; University of Calgary; University of Saskatchewan; Université Laval; Université de Montréal; Providence Health Care Research Institute","funders":"National Institute on Minority Health and Health Disparities; National Center for Research Resources; National Institute of Neurological Disorders and Stroke; National Institute of Arthritis and Musculoskeletal and Skin Diseases; National Institute of Allergy and Infectious Diseases; National Center for Advancing Translational Sciences; National Human Genome Research Institute; National Heart, Lung, and Blood Institute; National Institute on Aging; National Cancer Institute; Mississippi State Department of Health; National Institute of Environmental Health Sciences; Frederick National Laboratory for Cancer Research; National Institute of Diabetes and Digestive and Kidney Diseases; Jackson State University; Wake Forest University; American Diabetes Association; National Institutes of Health; U.S. Department of Health and Human Services","keywords":"Biology; Host (biology); Human immunodeficiency virus (HIV); Diversity (politics); Human leukocyte antigen; Population; Evolutionary biology; Computational biology; Genetics; Resolution (logic); High resolution; Virology; Remote sensing; Environmental health; Antigen; Computer science","score_opus":0.034012655127558765,"score_gpt":0.25128602808585593,"score_spread":0.21727337295829716,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W3203889005","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.84471333,0.0016179824,0.14195064,0.00027451362,0.00008915247,0.00005872837,0.005630417,0.00063541793,0.005029828],"genre_scores_gemma":[0.93020374,0.0004827524,0.061233636,0.0003103539,0.00005410679,0.000070329654,0.005336547,0.00014068632,0.002167929],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9994642,0.00013592503,0.000026314934,0.00020260611,0.000101615056,0.00006935184],"domain_scores_gemma":[0.99943215,0.00016118442,0.00006351661,0.00019998926,0.00009694516,0.00004616932],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0011342868,0.0003212549,0.00042104896,0.001056626,0.00037270878,0.0009512319,0.0005621468,0.00068914506,0.0019973961],"category_scores_gemma":[0.0013663853,0.0003654038,0.00032895443,0.0009824651,0.00020126077,0.0003606956,0.0007603104,0.0008049714,0.00068411854],"study_design_candidate":"bench_or_experimental","study_design_consensus":"bench_or_experimental","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00048389714,0.00015557733,0.062268335,0.00009469056,0.0002923506,0.0003035107,0.0002896829,0.008440812,0.8020268,0.002630784,0.002750989,0.12026251],"study_design_scores_gemma":[0.00019758807,0.00091924326,0.5519507,0.00012920338,0.0009947488,0.0044559315,0.00045244902,0.07893544,0.3080853,0.010440591,0.04326214,0.0001768146],"about_ca_topic_score_codex":0.0016358295,"about_ca_topic_score_gemma":0.0033218153,"teacher_disagreement_score":0.0019973961,"about_ca_system_score_codex":0.00019385369,"about_ca_system_score_gemma":0.00021057604,"threshold_uncertainty_score":0.006681919},"labels":[],"label_agreement":null},{"id":"W3205195294","doi":"10.1038/s41588-021-00928-6","title":"Mutational signatures in esophageal squamous cell carcinoma from eight countries with varying incidence","year":2021,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Cancer Genomics and Diagnostics","field":"Biochemistry, Genetics and Molecular Biology","cited_by":198,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University Health Network","funders":"NIHR Cambridge Biomedical Research Centre; Wellcome Trust; Japan Agency for Medical Research and Development; Medical Research Council; Wellcome; Alfred P. Sloan Foundation; World Health Organization; National Cancer Institute; Cancer Research UK; U.S. Department of Health and Human Services","keywords":"Biology; Incidence (geometry); Esophageal squamous cell carcinoma; Basal cell; Carcinoma; Genetics; Cancer research; Internal medicine","score_opus":0.0035914779708118303,"score_gpt":0.21765272049008447,"score_spread":0.21406124251927264,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W3205195294","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99898356,0.00017798989,0.000101689475,0.0000075646026,0.0000013120135,0.000005210238,0.0005335134,0.0000025909703,0.00018655013],"genre_scores_gemma":[0.99850804,0.00013814775,0.00023676155,0.00001446634,0.0000012071567,0.0000069560947,0.0010275713,0.000002982037,0.00006374266],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9994174,0.00018687568,0.000072135685,0.00015774496,0.00007993027,0.0000859854],"domain_scores_gemma":[0.99916565,0.00020479188,0.00029943895,0.00011896633,0.00014575476,0.00006534764],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00054154714,0.00021565684,0.00034928604,0.0015235621,0.00029612222,0.0006517131,0.00016346642,0.00027281579,0.00057458377],"category_scores_gemma":[0.0017195564,0.0002251371,0.0003927089,0.0020088034,0.00029908237,0.00018342149,0.0005395259,0.00017665837,0.00010961326],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00016260333,0.000011535368,0.99052715,0.00004337869,0.00020409252,0.00020475085,0.00035803454,0.00025265303,0.003432066,0.000040087372,0.00008527954,0.0046784678],"study_design_scores_gemma":[0.000004277507,0.00004665905,0.9982243,0.00000937857,0.000059841634,0.00041016663,0.000422417,0.00009734984,0.00037597894,0.000014780813,0.00033065295,0.000004193356],"about_ca_topic_score_codex":0.00483478,"about_ca_topic_score_gemma":0.00574944,"teacher_disagreement_score":0.00483478,"about_ca_system_score_codex":0.00026012692,"about_ca_system_score_gemma":0.0001654209,"threshold_uncertainty_score":0.0096132755},"labels":[],"label_agreement":null},{"id":"W3210241491","doi":"10.1038/s41588-021-00979-9","title":"Author Correction: A high-resolution HLA reference panel capturing global population diversity enables multi-ancestry fine-mapping in HIV host response","year":2021,"lang":"en","type":"erratum","venue":"Nature Genetics","topic":"HIV Research and Treatment","field":"Immunology and Microbiology","cited_by":4,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Manitoba; Public Health Agency of Canada; University of Ottawa; McGill University; University of Calgary; University of Saskatchewan; Université Laval; Université de Montréal; Providence Health Care Research Institute","funders":"National Institute of Arthritis and Musculoskeletal and Skin Diseases; National Institute on Aging; National Cancer Institute; U.S. Department of Health and Human Services; National Institutes of Health; National Institute of Allergy and Infectious Diseases; Wake Forest University; American Diabetes Association","keywords":"Biology; Human immunodeficiency virus (HIV); Host (biology); Diversity (politics); Human leukocyte antigen; Computational biology; High resolution; Host response; Population; Evolutionary biology; Resolution (logic); Genetics; Virology; Computer science; Remote sensing; Immune system; Demography; Artificial intelligence; Antigen; Geography; Political science","score_opus":0.05008388633912166,"score_gpt":0.2984966165639081,"score_spread":0.2484127302247864,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W3210241491","genre_codex":"editorial","genre_gemma":"other","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"other","genre_consensus":null,"domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.00019246689,0.0007964976,0.0010353769,0.050565045,0.94360036,0.000017671551,0.0010888254,0.00026948072,0.0024343068],"genre_scores_gemma":[0.024791373,0.0084164785,0.011587806,0.16888733,0.463851,0.00026393245,0.003588826,0.0031642204,0.31544906],"study_design_codex":"not_applicable","study_design_gemma":"not_applicable","domain_scores_codex":[0.99657816,0.0005751791,0.00055521505,0.0005200031,0.0014792157,0.0002923535],"domain_scores_gemma":[0.976127,0.007566523,0.0011999932,0.0014978301,0.012616875,0.000991868],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0038900652,0.0017838929,0.0015020925,0.002645432,0.0028965273,0.0034206246,0.0028659538,0.0066804327,0.038244165],"category_scores_gemma":[0.058163673,0.0011419246,0.0012748586,0.0014512602,0.0018961745,0.0016239826,0.0016422268,0.012127102,0.02249338],"study_design_candidate":"not_applicable","study_design_consensus":"not_applicable","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00002887766,0.0000037954023,0.00010329483,0.0000712138,0.000012561199,0.0005090863,0.000027212107,0.000041195857,0.000045641336,0.00059649907,0.9943948,0.0041658017],"study_design_scores_gemma":[0.0000603566,0.000014203822,0.0007476146,0.0003535756,0.00006525283,0.0019118419,0.000086740605,0.0003473579,0.0005178836,0.0018830032,0.99397415,0.000038078484],"about_ca_topic_score_codex":0.01744009,"about_ca_topic_score_gemma":0.024492677,"teacher_disagreement_score":0.038244165,"about_ca_system_score_codex":0.0030295353,"about_ca_system_score_gemma":0.0041682743,"threshold_uncertainty_score":0.12793946},"labels":[],"label_agreement":null},{"id":"W3212913189","doi":"10.1038/s41588-021-00964-2","title":"A cis-acting mechanism mediates transcriptional memory at Polycomb target genes in mammals","year":2021,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Genomics and Chromatin Dynamics","field":"Biochemistry, Genetics and Molecular Biology","cited_by":91,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"IONICS Mass Spectrometry (Canada)","funders":"Biotechnology and Biological Sciences Research Council; Agence Nationale de la Recherche","keywords":"Biology; Epigenetics; Polycomb-group proteins; Chromatin; Histone; Genetics; Regulation of gene expression; Transcriptional regulation; Cell biology; Gene silencing; Gene; Transcription factor; Transcription (linguistics); Repressor","score_opus":0.005649386271517276,"score_gpt":0.2234271935161079,"score_spread":0.21777780724459062,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W3212913189","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9590765,0.0031853355,0.031808913,0.00042417643,0.00015843197,0.00003629649,0.00034397765,0.0006907537,0.0042755464],"genre_scores_gemma":[0.99351513,0.000284013,0.0034047007,0.00012157485,0.00004072096,0.000018803243,0.00018641433,0.000038453694,0.0023902175],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99976283,0.00001700698,0.000014124853,0.000109989414,0.000054202617,0.000041773957],"domain_scores_gemma":[0.9995161,0.000092817216,0.00008648126,0.00012981173,0.000062493375,0.00011226323],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00029750427,0.00023788826,0.0004196883,0.00033037312,0.0004969171,0.00069515756,0.0010149224,0.0007138967,0.001852174],"category_scores_gemma":[0.00044556634,0.0005381443,0.00034633235,0.00019442363,0.00069030956,0.00076112925,0.00073486875,0.0009596674,0.0010983496],"study_design_candidate":"bench_or_experimental","study_design_consensus":"bench_or_experimental","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00008686593,0.000010882765,0.001081735,0.000035808287,0.0000108753775,0.00010022858,0.000044448472,0.00010251965,0.9935069,0.0018625836,0.000058990103,0.0030981367],"study_design_scores_gemma":[0.0000315626,0.00020083073,0.0340788,0.00001757259,0.000035154822,0.00083759904,0.0001160631,0.0023507667,0.9578409,0.0022332005,0.0022306154,0.000026944346],"about_ca_topic_score_codex":0.00040676052,"about_ca_topic_score_gemma":0.0009963808,"teacher_disagreement_score":0.001852174,"about_ca_system_score_codex":0.00030569293,"about_ca_system_score_gemma":0.00024506834,"threshold_uncertainty_score":0.006196201},"labels":[],"label_agreement":null},{"id":"W4206349208","doi":"10.1038/s41588-021-00969-x","title":"Genetic variation influencing DNA methylation provides insights into molecular mechanisms regulating genomic function","year":2022,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Epigenetics and DNA Methylation","field":"Biochemistry, Genetics and Molecular Biology","cited_by":172,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Université de Montréal; Centre Hospitalier Universitaire Sainte-Justine; SickKids Foundation; Hospital for Sick Children; University of Toronto","funders":"National Heart, Lung, and Blood Institute; National Medical Research Council; Biotechnology and Biological Sciences Research Council; Agence Nationale de la Recherche; National Institute of Mental Health; Medical Research Council; National Institute for Health and Care Research; British Heart Foundation; Wellcome Trust","keywords":"Biology; DNA methylation; Genetics; Epigenomics; Quantitative trait locus; CpG site; Chromatin immunoprecipitation; Differentially methylated regions; Chromatin; Phenotype; Genome-wide association study; Gene; Single-nucleotide polymorphism; Gene expression; Genotype; Promoter","score_opus":0.005133317071440917,"score_gpt":0.2262729440298347,"score_spread":0.2211396269583938,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4206349208","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.94231766,0.0030892645,0.045969278,0.00074865686,0.00013241783,0.000015736476,0.0013139425,0.00035005668,0.00606293],"genre_scores_gemma":[0.99236214,0.0009613336,0.005332454,0.000087550085,0.000036219404,0.000006566663,0.00025163364,0.000041495863,0.0009206584],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.99980277,0.00004333534,0.000010704829,0.00006788928,0.000051578485,0.000023681287],"domain_scores_gemma":[0.99970526,0.00014154182,0.000059752412,0.00004142056,0.000016898992,0.000035111527],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00035214136,0.00030108445,0.00030791594,0.0006945682,0.00020250019,0.00049571006,0.00037890766,0.0004766001,0.0015754759],"category_scores_gemma":[0.0005158534,0.00022542129,0.00020859588,0.00066003716,0.0004557918,0.00037043073,0.0003354117,0.00060174183,0.00021045702],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00017634204,0.000019295529,0.0063869935,0.000035555902,0.000038345937,0.00015157813,0.000057749043,0.00072608027,0.97574526,0.0065145404,0.000096804375,0.010051338],"study_design_scores_gemma":[0.000049924565,0.00023573845,0.20291968,0.000023041433,0.00017541967,0.0014003795,0.00016699487,0.01190729,0.7557461,0.017977558,0.009310216,0.00008764114],"about_ca_topic_score_codex":0.001160319,"about_ca_topic_score_gemma":0.0018810484,"teacher_disagreement_score":0.0015754759,"about_ca_system_score_codex":0.00037416906,"about_ca_system_score_gemma":0.00018544028,"threshold_uncertainty_score":0.005270481},"labels":[],"label_agreement":null},{"id":"W4206666463","doi":"10.1038/s41588-021-00998-6","title":"Author Correction: Gain-of-function variants in SYK cause immune dysregulation and systemic inflammation in humans and mice","year":2022,"lang":"en","type":"erratum","venue":"Nature Genetics","topic":"Cell Adhesion Molecules Research","field":"Medicine","cited_by":2,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Ontario Institute for Cancer Research; Université de Montréal; Princess Margaret Cancer Centre; St. Michael's Hospital; Hospital for Sick Children; Centre Hospitalier Universitaire Sainte-Justine; McMaster University; University Health Network; University of Toronto; SickKids Foundation","funders":"Wellcome Trust","keywords":"Systemic inflammation; Biology; Inflammation; Immune system; Immune dysregulation; Syk; Gain of function; Function (biology); Immunology; Genetics; Mutation; Gene; Signal transduction","score_opus":0.01505812674485354,"score_gpt":0.2956751585421201,"score_spread":0.2806170317972666,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4206666463","genre_codex":"editorial","genre_gemma":"other","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"other","genre_consensus":null,"domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.00038538466,0.00071100815,0.0012332521,0.032240454,0.96178645,0.00001797387,0.0011857479,0.00048379687,0.0019559674],"genre_scores_gemma":[0.044067558,0.010879436,0.017156955,0.10736786,0.40837693,0.0003381241,0.0069542676,0.005390138,0.39946878],"study_design_codex":"not_applicable","study_design_gemma":"not_applicable","domain_scores_codex":[0.9967403,0.00040660924,0.0004942159,0.0005271666,0.0015470082,0.0002847654],"domain_scores_gemma":[0.98360866,0.0050439173,0.0011630591,0.0011377161,0.008016396,0.0010302354],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0029836828,0.0022883585,0.0017991207,0.0027169178,0.0025709365,0.0027163376,0.003070304,0.0065823807,0.044682357],"category_scores_gemma":[0.032732133,0.001159699,0.00165774,0.0014250823,0.0018593982,0.0014210173,0.0016718006,0.009388381,0.022714661],"study_design_candidate":"not_applicable","study_design_consensus":"not_applicable","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00007010408,0.00000929355,0.00013955364,0.00012870465,0.00003357019,0.0014570022,0.00004054876,0.00006332766,0.0002568175,0.0008091103,0.991454,0.0055379206],"study_design_scores_gemma":[0.0001183533,0.000039147806,0.0011122078,0.0003254668,0.00013069868,0.0043630847,0.00010810849,0.0003734792,0.0015831526,0.0016364204,0.9901427,0.00006705814],"about_ca_topic_score_codex":0.009311486,"about_ca_topic_score_gemma":0.013636881,"teacher_disagreement_score":0.044682357,"about_ca_system_score_codex":0.00274202,"about_ca_system_score_gemma":0.003384335,"threshold_uncertainty_score":0.14947736},"labels":[],"label_agreement":null},{"id":"W4206699848","doi":"10.1038/s41588-021-00996-8","title":"Multi-ancestry fine mapping implicates OAS1 splicing in risk of severe COVID-19","year":2022,"lang":"en","type":"article","venue":"Nature Genetics","topic":"RNA regulation and disease","field":"Biochemistry, Genetics and Molecular Biology","cited_by":128,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"McGill University; Jewish General Hospital","funders":"Health Data Research UK; CIHR Skin Research Training Centre; National Institute of General Medical Sciences; Japan Society for the Promotion of Science; National Center for Advancing Translational Sciences; Medical Research Council; Fonds de Recherche du Québec - Santé; Perelman School of Medicine, University of Pennsylvania; Magnus Bergvalls Stiftelse; Fonds de Recherche du Québec-Société et Culture; NordForsk; Vetenskapsrådet; European Commission; Research Councils UK; Canadian Institutes of Health Research; Compute Canada; Biotechnology and Biological Sciences Research Council; Wellcome Trust; Cancer Research UK; University of Pennsylvania; Public Health Agency; National Institute of Diabetes and Digestive and Kidney Diseases; Government of Canada; McGill University; Public Health Agency of Canada; Regeneron Pharmaceuticals; National Institutes of Health; U.S. Department of Health and Human Services; Jewish General Hospital; King's College London; Jeanssons Stiftelser; National Institute for Health and Care Research","keywords":"Biology; Haplotype; Locus (genetics); Genetics; SNP; Gene; Coronavirus disease 2019 (COVID-19); splice; Single-nucleotide polymorphism; Genotype; Disease; Infectious disease (medical specialty)","score_opus":0.01645027499960432,"score_gpt":0.2974348891355195,"score_spread":0.2809846141359152,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4206699848","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99889416,0.00010164305,0.00046331107,0.00002797253,0.0000028114314,0.0000038140452,0.000068397,0.0000067340484,0.00043117994],"genre_scores_gemma":[0.9994949,0.00004210071,0.00024259122,0.000008769442,0.0000031621184,0.000001588308,0.00005860482,0.0000039504434,0.00014433287],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9997198,0.000065092834,0.000024340632,0.00008895591,0.00005904948,0.00004286937],"domain_scores_gemma":[0.99948263,0.000116800074,0.00023023385,0.00004037315,0.00003638076,0.00009359837],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0002805443,0.00039800207,0.00025166143,0.0010187343,0.000475212,0.00040842916,0.00023338938,0.00047526543,0.0025301424],"category_scores_gemma":[0.00077578047,0.00016621302,0.00032124415,0.0004847779,0.00032091173,0.000109681445,0.00045073428,0.0003609577,0.00018534006],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0009760265,0.0000689071,0.7239594,0.000043255273,0.0002470533,0.0036299115,0.0005242118,0.00040076397,0.25964338,0.00047582187,0.0001858316,0.009845395],"study_design_scores_gemma":[0.000023227676,0.00017160115,0.98483366,0.000015776537,0.0000917249,0.004656767,0.00015089787,0.0006360561,0.008729165,0.00025197575,0.00043019347,0.000009135096],"about_ca_topic_score_codex":0.0018678069,"about_ca_topic_score_gemma":0.0022949993,"teacher_disagreement_score":0.0025301424,"about_ca_system_score_codex":0.00013402772,"about_ca_system_score_gemma":0.00010980146,"threshold_uncertainty_score":0.008464098},"labels":[],"label_agreement":null},{"id":"W4206821853","doi":"10.1038/s41588-021-00971-3","title":"Two divergent haplotypes from a highly heterozygous lychee genome suggest independent domestication events for early and late-maturing cultivars","year":2022,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Horticultural and Viticultural Research","field":"Agricultural and Biological Sciences","cited_by":240,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Ottawa","funders":"","keywords":"Domestication; Biology; Cultivar; Loss of heterozygosity; Haplotype; Population; Allele; Genome; Genetics; Botany; Gene","score_opus":0.018787455766301316,"score_gpt":0.27171069460697883,"score_spread":0.2529232388406775,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4206821853","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99800676,0.00007095199,0.00100755,0.0000143385405,0.0000030777228,0.000009391041,0.0004524674,0.000019561228,0.00041591338],"genre_scores_gemma":[0.99571335,0.00004378851,0.0014084455,0.000042596905,0.0000029199032,0.000013776932,0.002100599,0.000017301481,0.0006571262],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.999946,0.0000048770917,0.000004527548,0.000024171493,0.00000772658,0.000012613855],"domain_scores_gemma":[0.9998541,0.00004177809,0.00003565449,0.000017721935,0.000016335931,0.000034388864],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00009154549,0.00015954289,0.0001982753,0.00035573792,0.00024801743,0.00018357475,0.000122024736,0.00023690074,0.0011742652],"category_scores_gemma":[0.00017052577,0.00013179844,0.00021926072,0.0002598981,0.00016957706,0.00011751398,0.00027159136,0.0002957746,0.0002021462],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00020193125,0.000016171261,0.024407815,0.00004568534,0.000023923772,0.00027115765,0.00022756046,0.0000749012,0.970611,0.0001467163,0.00004750823,0.003925682],"study_design_scores_gemma":[0.00004122914,0.00015285607,0.92769575,0.00002121827,0.000077135934,0.0018017048,0.00031562275,0.00083190104,0.0652176,0.00024105841,0.0035805285,0.000023293267],"about_ca_topic_score_codex":0.00043143655,"about_ca_topic_score_gemma":0.0016566095,"teacher_disagreement_score":0.0011742652,"about_ca_system_score_codex":0.00011622438,"about_ca_system_score_gemma":0.000094873365,"threshold_uncertainty_score":0.0039283037},"labels":[],"label_agreement":null},{"id":"W4210768242","doi":"10.1038/s41588-022-01020-3","title":"Author Correction: Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology","year":2022,"lang":"en","type":"erratum","venue":"Nature Genetics","topic":"Amyotrophic Lateral Sclerosis Research","field":"Medicine","cited_by":4,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"McGill University; Montreal Neurological Institute and Hospital","funders":"Medical Research Council; Rosetrees Trust; Agence Nationale de la Recherche; Motor Neurone Disease Association; Parkinson's UK; National Institute for Health and Care Research","keywords":"Amyotrophic lateral sclerosis; Biology; Genome-wide association study; Genetics; Association (psychology); Genetic association; Computational biology; Neuroscience; Evolutionary biology; Single-nucleotide polymorphism; Gene; Disease; Genotype; Internal medicine","score_opus":0.0305933821869309,"score_gpt":0.3224574372447373,"score_spread":0.2918640550578064,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4210768242","genre_codex":"editorial","genre_gemma":"other","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"other","genre_consensus":null,"domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.00043466518,0.00062824803,0.0022453512,0.042407934,0.9500243,0.000025572795,0.0016013964,0.0006900593,0.0019424455],"genre_scores_gemma":[0.047245886,0.010416852,0.025791235,0.114570215,0.40420583,0.00042360887,0.010203032,0.0076542143,0.37948903],"study_design_codex":"not_applicable","study_design_gemma":"not_applicable","domain_scores_codex":[0.99495536,0.00071998197,0.0009111047,0.0009318458,0.0020933705,0.00038821503],"domain_scores_gemma":[0.96827734,0.008537408,0.0017874998,0.0019286069,0.018051893,0.0014172094],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0045727096,0.0022764879,0.0017807982,0.002815625,0.0033725745,0.0036446254,0.0038049354,0.005462874,0.061887354],"category_scores_gemma":[0.060174484,0.0011265132,0.0014333464,0.0024729948,0.0020765471,0.0018618931,0.0019284419,0.011310704,0.030240297],"study_design_candidate":"not_applicable","study_design_consensus":"not_applicable","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00005147938,0.00000700739,0.00013102988,0.000111167144,0.000017856015,0.00060147594,0.000051964198,0.00005939276,0.0001346907,0.0007915074,0.9926158,0.005426676],"study_design_scores_gemma":[0.0000981724,0.000033785633,0.001231572,0.00048820933,0.000102307014,0.0037523538,0.00015830576,0.00062731275,0.0012018473,0.0031153054,0.98910224,0.00008852608],"about_ca_topic_score_codex":0.011994059,"about_ca_topic_score_gemma":0.0153658455,"teacher_disagreement_score":0.061887354,"about_ca_system_score_codex":0.0031964504,"about_ca_system_score_gemma":0.0052380837,"threshold_uncertainty_score":0.20703381},"labels":[],"label_agreement":null},{"id":"W4213416315","doi":"10.1038/s41588-021-01007-6","title":"Genome-wide association analyses identify new Brugada syndrome risk loci and highlight a new mechanism of sodium channel regulation in disease susceptibility","year":2022,"lang":"en","type":"review","venue":"Nature Genetics","topic":"Cardiac electrophysiology and arrhythmias","field":"Medicine","cited_by":142,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Western University; Université de Montréal; Montreal Heart Institute","funders":"National Institute of General Medical Sciences; National Human Genome Research Institute; Münchner Zentrum für Gesundheitswissenschaften; Helmholtz Zentrum München; Amsterdam Cardiovascular Sciences, Amsterdam University Medical Centers; National Institutes of Health; University College London Hospitals NHS Foundation Trust; Centre National de la Recherche Scientifique; Fonds Wetenschappelijk Onderzoek; Horizon 2020 Framework Programme; KU Leuven; Fondation pour la Recherche Médicale; ZonMw; Institut National de la Santé et de la Recherche Médicale; CHIST-ERA; Agence Nationale de la Recherche; Fondation Leducq; European Society of Cardiology; National Heart, Lung, and Blood Institute; Health~Holland; European Commission; American Heart Association; Broad Institute; Heart Rhythm Society; Deutsches Zentrum für Herz-Kreislaufforschung; Innoviris; Foundation for Cardiovascular Research; Bundesministerium für Bildung und Forschung; National Institute for Health and Care Research; Fédération Française de Cardiologie; Bayer; British Heart Foundation; Wellcome Trust; Hjerteforeningen","keywords":"Biology; Brugada syndrome; Genome-wide association study; Mechanism (biology); Genetics; Disease; Genetic association; Sodium channel; Computational biology; Single-nucleotide polymorphism; Gene; Genotype; Neuroscience; Internal medicine; Sodium","score_opus":0.023086034372812973,"score_gpt":0.32123989189764196,"score_spread":0.298153857524829,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4213416315","genre_codex":"review","genre_gemma":"review","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"review","genre_consensus":"review","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.00017471291,0.99764854,0.00041344334,0.0006071439,0.00022575125,0.000003150942,0.000033706438,0.000014921011,0.0008785889],"genre_scores_gemma":[0.0010970776,0.99756134,0.00033320638,0.0002719813,0.00021728479,0.000005412353,0.00006155111,0.000002291763,0.00044978978],"study_design_codex":"design_other","study_design_gemma":"observational","domain_scores_codex":[0.9998449,0.000030795898,0.000023737774,0.000034172026,0.0000467939,0.000019548239],"domain_scores_gemma":[0.9995309,0.0002809993,0.000056122408,0.000012896993,0.00008309968,0.000036090983],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0007221974,0.0008624776,0.0015178352,0.0018411076,0.00016770358,0.0009290742,0.0008396599,0.001137522,0.0035522322],"category_scores_gemma":[0.00085235585,0.00018939878,0.00061215746,0.00157648,0.00043849385,0.0007367932,0.0005381895,0.0017714882,0.0016634063],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00012273734,0.000034201286,0.0006241516,0.008289901,0.00024931764,0.000490338,0.00003247703,0.0005170718,0.0025271222,0.0047126333,0.026943209,0.95545673],"study_design_scores_gemma":[0.000078752426,0.00013867745,0.0057678246,0.006645123,0.0006180279,0.005181148,0.00008432111,0.00033588777,0.00079345156,0.007925747,0.9723849,0.000046158963],"about_ca_topic_score_codex":0.0007869528,"about_ca_topic_score_gemma":0.0018157131,"teacher_disagreement_score":0.0035522322,"about_ca_system_score_codex":0.0004974619,"about_ca_system_score_gemma":0.0009176806,"threshold_uncertainty_score":0.011883378},"labels":[],"label_agreement":null},{"id":"W4220711675","doi":"10.1038/s41588-022-01016-z","title":"Polygenic prediction of educational attainment within and between families from genome-wide association analyses in 3 million individuals","year":2022,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Genetic Associations and Epidemiology","field":"Biochemistry, Genetics and Molecular Biology","cited_by":689,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Queen's University; University of Toronto","funders":"National Health and Medical Research Council; Australian Research Council; Medical Research Council; National Institute of Mental Health; Social Sciences and Humanities Research Council of Canada; Oulun Yliopisto; Department of Education and Training; Riksbankens Jubileumsfond; Vetenskapsrådet; Genome Canada; Lundbeckfonden; Erasmus Universiteit Rotterdam; University of South Australia; University of Queensland; National Institutes of Health; Open Philanthropy Project; Netherlands Heart Institute; Imperial College London; Ontario Genomics Institute; Nederlandse Organisatie voor Wetenschappelijk Onderzoek; Li Ka Shing Foundation; Steno Diabetes Center Copenhagen; National Institute on Aging; Pershing Square Foundation; Economic and Social Research Council; U.S. Department of Health and Human Services; School of Public Health, Imperial College London; Ontario Genomics; Ragnar Söderbergs stiftelse; Government of Canada","keywords":"Genome-wide association study; Biology; Single-nucleotide polymorphism; Genetics; Genetic association; Genome; Multifactorial Inheritance; Genotype; Gene","score_opus":0.01431886919613187,"score_gpt":0.2884911903171365,"score_spread":0.27417232112100465,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4220711675","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9966241,0.00031554096,0.0016977997,0.00014530777,0.000010987654,0.000005793251,0.00069663534,0.00004511636,0.00045887037],"genre_scores_gemma":[0.99802786,0.00013100072,0.0009429633,0.000052255098,0.000012215519,0.000009958138,0.0006211376,0.000010542062,0.00019186625],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9990753,0.00035682943,0.0000638377,0.00029764982,0.00010394307,0.00010242706],"domain_scores_gemma":[0.99828917,0.0007171433,0.0004473159,0.00023350878,0.00009121602,0.00022166921],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.001463195,0.0003758395,0.0003908307,0.00092466833,0.0006969483,0.00065086025,0.00032382619,0.00050022407,0.002347906],"category_scores_gemma":[0.004677505,0.0002241136,0.0008633014,0.0012633764,0.00034616797,0.00026396313,0.0007827612,0.00066387065,0.000318536],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00024156754,0.00003275337,0.987823,0.00002040378,0.0005912248,0.00036916469,0.00013620792,0.00056008424,0.0029312668,0.0003644112,0.0005148902,0.0064150165],"study_design_scores_gemma":[0.000030025123,0.000052440155,0.9945095,0.000016248268,0.00030224203,0.0004517226,0.00007867576,0.002260005,0.00048206653,0.0011139114,0.00069171283,0.00001129013],"about_ca_topic_score_codex":0.0045104735,"about_ca_topic_score_gemma":0.0069115027,"teacher_disagreement_score":0.0045104735,"about_ca_system_score_codex":0.00019446628,"about_ca_system_score_gemma":0.00024588683,"threshold_uncertainty_score":0.008968413},"labels":[],"label_agreement":null},{"id":"W4220827000","doi":"10.1038/s41588-021-00997-7","title":"Assessing the contribution of rare variants to complex trait heritability from whole-genome sequence data","year":2022,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Genetic Associations and Epidemiology","field":"Biochemistry, Genetics and Molecular Biology","cited_by":359,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Ottawa; McGill University; University of Calgary; University of Saskatchewan; Université de Montréal; Providence Health Care","funders":"National Institute of Environmental Health Sciences; National Institute of Diabetes and Digestive and Kidney Diseases; National Institute of General Medical Sciences; Westlake Education Foundation; Sylvia and Charles Viertel Charitable Foundation; National Institute of Mental Health; National Heart, Lung, and Blood Institute; National Institute on Aging; National Health and Medical Research Council; Australian Research Council; National Cancer Institute; U.S. Department of Health and Human Services; National Institutes of Health; U.S. Department of Veterans Affairs; Department of Education and Training","keywords":"Heritability; Biology; Linkage disequilibrium; Genetics; Minor allele frequency; Single-nucleotide polymorphism; Missing heritability problem; Genetic association; Genome-wide association study; Trait; Quantitative trait locus; Genotype; Gene","score_opus":0.051646863521671256,"score_gpt":0.3444017738858319,"score_spread":0.2927549103641606,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4220827000","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9215996,0.0017674858,0.07136288,0.00031922653,0.000072996416,0.000058637994,0.003438149,0.00032467349,0.0010563489],"genre_scores_gemma":[0.9837233,0.0004124935,0.012809946,0.00010608379,0.000060147664,0.00003561525,0.0025043085,0.00009546909,0.0002526086],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99150884,0.003978329,0.00078895903,0.002248753,0.0010485504,0.00042655648],"domain_scores_gemma":[0.9509063,0.04032498,0.0035675343,0.0034398737,0.0011273464,0.0006339731],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.010588678,0.00090942415,0.0012268166,0.00446461,0.0007169084,0.001709901,0.0011109038,0.0013531464,0.0022782658],"category_scores_gemma":[0.040417142,0.00064046076,0.0017005256,0.0042684856,0.00086882786,0.0010832719,0.0012294105,0.001630319,0.00047438263],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00062075886,0.00008007131,0.9134731,0.00034585642,0.006149333,0.0012832049,0.0003914646,0.007726832,0.02747451,0.0014402242,0.0006501869,0.040364392],"study_design_scores_gemma":[0.00013699433,0.00024004877,0.9422572,0.00011902718,0.0032218904,0.0026525394,0.00025796052,0.03618923,0.004561599,0.007612474,0.002651931,0.000099103076],"about_ca_topic_score_codex":0.005358574,"about_ca_topic_score_gemma":0.0070446837,"teacher_disagreement_score":0.010588678,"about_ca_system_score_codex":0.00025799483,"about_ca_system_score_gemma":0.00063200464,"threshold_uncertainty_score":0.05599892},"labels":[],"label_agreement":null},{"id":"W4221073172","doi":"10.1038/s41588-022-01025-y","title":"Genetic associations at regulatory phenotypes improve fine-mapping of causal variants for 12 immune-mediated diseases","year":2022,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Genetic Associations and Epidemiology","field":"Biochemistry, Genetics and Molecular Biology","cited_by":73,"is_retracted":false,"has_abstract":false,"route_ca_aff":false,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"","funders":"Canadian Institutes of Health Research; British Heart Foundation; Wellcome Trust","keywords":"Biology; Quantitative trait locus; Genetics; Expression quantitative trait loci; Computational biology; Indel; Locus (genetics); Genome-wide association study; Gene; Single-nucleotide polymorphism; Genotype","score_opus":0.008000284603734012,"score_gpt":0.2465113932783396,"score_spread":0.2385111086746056,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4221073172","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9635038,0.0021177137,0.026861357,0.00066890963,0.00012075088,0.000049886326,0.0016989926,0.0002835686,0.004694992],"genre_scores_gemma":[0.98948705,0.0003542882,0.008506015,0.00022284867,0.00009805683,0.000020958896,0.00041061582,0.00008730134,0.0008128092],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99521196,0.0025313532,0.0003176397,0.0011916175,0.00040792394,0.00033960937],"domain_scores_gemma":[0.9857094,0.010006487,0.0019060996,0.0013525663,0.0005352341,0.00049019704],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0056651435,0.0013338856,0.0012438755,0.0032574884,0.00065788307,0.0015409874,0.0010612458,0.0015910805,0.0077719567],"category_scores_gemma":[0.01229192,0.0006525926,0.0016314128,0.0020104167,0.00084398227,0.0009597048,0.0016343413,0.002096667,0.0008625564],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0024136724,0.00040572602,0.8666881,0.0002596202,0.0026261755,0.0014280025,0.00036216775,0.004811417,0.06102491,0.003195179,0.001108155,0.05567685],"study_design_scores_gemma":[0.0003360603,0.00038570957,0.9567281,0.0000952699,0.0029628016,0.0024067087,0.00022870216,0.010718407,0.009724279,0.010403467,0.005941079,0.00006951355],"about_ca_topic_score_codex":0.0020848797,"about_ca_topic_score_gemma":0.002880421,"teacher_disagreement_score":0.0077719567,"about_ca_system_score_codex":0.00024226563,"about_ca_system_score_gemma":0.0004020626,"threshold_uncertainty_score":0.029960454},"labels":[],"label_agreement":null},{"id":"W4223591189","doi":"10.1038/s41588-022-01024-z","title":"New insights into the genetic etiology of Alzheimer’s disease and related dementias","year":2022,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Genetic Associations and Epidemiology","field":"Biochemistry, Genetics and Molecular Biology","cited_by":2471,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Université de Montréal; Centre Hospitalier Universitaire Sainte-Justine; Hospital for Sick Children; Occupational Cancer Research Centre; SickKids Foundation; University of Toronto","funders":"National Institute on Minority Health and Health Disparities; National Institute of Neurological Disorders and Stroke; Rheinische Friedrich-Wilhelms-Universität Bonn; Universitat de Barcelona; National Heart, Lung, and Blood Institute; Centro de Investigación Biomédica en Red Diabetes y Enfermedades Metabólicas Asociadas; Deutsches Zentrum für Neurodegenerative Erkrankungen; Motor Neurone Disease Association; National Institute on Aging; National Institute for Health and Care Research; Universität zu Köln; National and Kapodistrian University of Athens; McLean Hospital; Université de Lille; University of Washington; Région Normandie; Harokopio University; Howard Hughes Medical Institute; Development of Innovative Strategies for a Transdisciplinary approach to ALZheimer's disease; Universität Duisburg-Essen; Agence Nationale de la Recherche; Biotechnology and Biological Sciences Research Council; Wellcome Trust; School of Medicine, Boston University; Lundbeckfonden; Institut National de la Santé et de la Recherche Médicale; Università degli Studi di Cagliari; Medical Research Council","keywords":"Biology; Etiology; Disease; Alzheimer's disease; Genetics; Bioinformatics; Pathology; Medicine","score_opus":0.008065599664773862,"score_gpt":0.25774134915895663,"score_spread":0.24967574949418278,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4223591189","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9631739,0.024244169,0.006289598,0.0029421907,0.00008877827,0.000017841014,0.0005241114,0.00005277842,0.0026666638],"genre_scores_gemma":[0.9818525,0.0125482,0.00363328,0.00060924696,0.00031610238,0.000010879847,0.00041852528,0.000013288179,0.00059799606],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9993548,0.0002419932,0.000058549234,0.00013366569,0.00015642027,0.000054678705],"domain_scores_gemma":[0.9987785,0.0007269604,0.00021866479,0.000107540654,0.00008684325,0.00008143431],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0014854218,0.0007414416,0.0006973559,0.0022084056,0.00027889886,0.000881941,0.00040831763,0.00051224494,0.0016468953],"category_scores_gemma":[0.0033356703,0.00026308175,0.0006370959,0.0017218654,0.000960428,0.0009072129,0.00064386934,0.0006520548,0.00017827963],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0017132029,0.0003077271,0.8133331,0.00045929695,0.0016588375,0.004238338,0.0010398952,0.004234968,0.015594714,0.011442575,0.0016566638,0.1443206],"study_design_scores_gemma":[0.0001362502,0.00031501375,0.9478313,0.00021036295,0.0008189596,0.004585576,0.0006703806,0.0041842507,0.0012421355,0.03207784,0.007870043,0.00005803808],"about_ca_topic_score_codex":0.002939609,"about_ca_topic_score_gemma":0.0043430272,"teacher_disagreement_score":0.002939609,"about_ca_system_score_codex":0.0003124409,"about_ca_system_score_gemma":0.0005428805,"threshold_uncertainty_score":0.007855773},"labels":[],"label_agreement":null},{"id":"W4223601910","doi":"10.1038/s41588-022-01046-7","title":"Genome-edited crops for improved food security of smallholder farmers","year":2022,"lang":"en","type":"article","venue":"Nature Genetics","topic":"CRISPR and Genetic Engineering","field":"Biochemistry, Genetics and Molecular Biology","cited_by":154,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Saskatchewan","funders":"Genome Canada; Bill and Melinda Gates Foundation","keywords":"Food security; Sustainability; Biology; Diversification (marketing strategy); Agriculture; Enthusiasm; Agricultural diversification; Natural resource economics; License; Genome; Biotechnology; Business; Economics; Political science; Ecology; Gene; Genetics","score_opus":0.005213833922393772,"score_gpt":0.2637700204765642,"score_spread":0.25855618655417045,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4223601910","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9407879,0.002099742,0.04248451,0.0022589115,0.00037152533,0.00013531357,0.0012104062,0.0005154332,0.01013623],"genre_scores_gemma":[0.9695376,0.0011151984,0.018741958,0.00021097725,0.000022821056,0.000042957367,0.00057157665,0.00008322985,0.009673767],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9998467,0.000028372539,0.0000074290624,0.00003583319,0.000045041263,0.000036591686],"domain_scores_gemma":[0.99984586,0.00004496706,0.000039447765,0.000024096234,0.000017607372,0.000028005166],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0004002967,0.00028825115,0.00021696482,0.00025687,0.0003283062,0.0006450394,0.0004676658,0.0005999529,0.0042191125],"category_scores_gemma":[0.00034803743,0.000109836656,0.00018701244,0.00026663495,0.00025472333,0.00045992451,0.000669346,0.00077188585,0.00049053115],"study_design_candidate":"bench_or_experimental","study_design_consensus":"bench_or_experimental","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00015041698,0.000058532976,0.00038630774,0.00007081795,0.0000192506,0.00023030447,0.00007597533,0.00052741054,0.980518,0.0022475591,0.000528013,0.015187412],"study_design_scores_gemma":[0.00018793417,0.00066126336,0.013179444,0.000087218905,0.00013939549,0.0010086987,0.00077864353,0.005434284,0.8944604,0.0059027565,0.078096546,0.00006342715],"about_ca_topic_score_codex":0.0005302661,"about_ca_topic_score_gemma":0.0014091576,"teacher_disagreement_score":0.0042191125,"about_ca_system_score_codex":0.0004218565,"about_ca_system_score_gemma":0.00034008693,"threshold_uncertainty_score":0.01411432},"labels":[],"label_agreement":null},{"id":"W4224016686","doi":"10.1038/s41588-022-01041-y","title":"Breast tumor microenvironment structures are associated with genomic features and clinical outcome","year":2022,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Single-cell and spatial transcriptomics","field":"Biochemistry, Genetics and Molecular Biology","cited_by":273,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of British Columbia; BC Cancer Agency","funders":"Cancer Research UK Cambridge Institute, University of Cambridge; NIHR Cambridge Biomedical Research Centre; Medical Research Council; National Institute for Health and Care Research; Department of Health and Social Care; Cancer Research UK","keywords":"Biology; Tumor microenvironment; Stromal cell; Multicellular organism; Immune system; Breast cancer; Estrogen receptor; Cancer research; Cancer; Genetics; Gene","score_opus":0.009318763881013591,"score_gpt":0.24327846255070387,"score_spread":0.23395969866969027,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4224016686","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99831724,0.00025348406,0.0009068865,0.000020437586,0.0000013898008,0.000003385689,0.00017216912,0.000019037467,0.0003059442],"genre_scores_gemma":[0.99943453,0.000059428316,0.00028950526,0.000005428989,0.0000018605162,0.0000026163225,0.000106951375,0.0000038031812,0.00009583385],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99984884,0.000025046396,0.0000103663315,0.000054522505,0.000033068813,0.000028157683],"domain_scores_gemma":[0.9995828,0.0001010783,0.00020736696,0.00003706648,0.00003187031,0.00003983557],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00017284475,0.00010670843,0.00019062423,0.0006099522,0.000106332096,0.00032654378,0.00010651202,0.0001799271,0.0009703314],"category_scores_gemma":[0.00051573344,0.000091340225,0.00011421721,0.00044983742,0.00020085895,0.0001379153,0.00021195224,0.00018914322,0.00013773577],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00051747833,0.000022642353,0.7697421,0.000038339884,0.00011731253,0.00024900233,0.0001057704,0.0005574469,0.21335377,0.00012337565,0.00011578967,0.015056959],"study_design_scores_gemma":[0.0000022096679,0.00004648975,0.98768693,0.0000021742237,0.00003067213,0.0005761881,0.00007442138,0.0007793803,0.010441169,0.00012253909,0.00023410661,0.0000037103425],"about_ca_topic_score_codex":0.00045318398,"about_ca_topic_score_gemma":0.0008896069,"teacher_disagreement_score":0.0009703314,"about_ca_system_score_codex":0.00013765515,"about_ca_system_score_gemma":0.00006738238,"threshold_uncertainty_score":0.003246069},"labels":[],"label_agreement":null},{"id":"W4224980373","doi":"10.1038/s41588-022-01079-y","title":"Author Correction: Genome-wide association analyses identify new Brugada syndrome risk loci and highlight a new mechanism of sodium channel regulation in disease susceptibility","year":2022,"lang":"en","type":"erratum","venue":"Nature Genetics","topic":"Cardiac electrophysiology and arrhythmias","field":"Medicine","cited_by":3,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Western University; Université de Montréal; Montreal Heart Institute","funders":"","keywords":"Brugada syndrome; Biology; Mechanism (biology); Genome-wide association study; Genetics; Sodium channel; Genetic association; Disease; Computational biology; Single-nucleotide polymorphism; Gene; Genotype; Neuroscience; Internal medicine; Sodium; Medicine","score_opus":0.01205044453900611,"score_gpt":0.2870150441770171,"score_spread":0.274964599638011,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4224980373","genre_codex":"editorial","genre_gemma":"other","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"other","genre_consensus":null,"domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.00024185826,0.0005262961,0.0011690451,0.038880844,0.9561391,0.000022902075,0.0011392019,0.00043338758,0.0014472847],"genre_scores_gemma":[0.037099,0.0064361566,0.018583741,0.12675285,0.49780613,0.0003541274,0.006078091,0.004476041,0.30241385],"study_design_codex":"not_applicable","study_design_gemma":"not_applicable","domain_scores_codex":[0.9961778,0.0006636262,0.0006631713,0.0006322674,0.0014421779,0.0004210614],"domain_scores_gemma":[0.9751091,0.0063824886,0.0012808186,0.0015816604,0.0142800035,0.0013659402],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0040858244,0.0025693537,0.002413192,0.003224752,0.002935426,0.003535231,0.0042645214,0.008231678,0.07045041],"category_scores_gemma":[0.052521512,0.0013983372,0.002146464,0.0019729882,0.0019325322,0.0018515235,0.0019141264,0.011593541,0.02458963],"study_design_candidate":"not_applicable","study_design_consensus":"not_applicable","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.000058299116,0.000007819797,0.00018234474,0.00014426158,0.000036638266,0.0010283745,0.000031083197,0.0000708487,0.000104678234,0.00065350323,0.992769,0.0049130768],"study_design_scores_gemma":[0.0003202373,0.00004689317,0.002426533,0.00065333047,0.00023500514,0.0055562253,0.00016641396,0.0009913828,0.0011060431,0.0038372756,0.9845467,0.00011384097],"about_ca_topic_score_codex":0.014839461,"about_ca_topic_score_gemma":0.02278761,"teacher_disagreement_score":0.07045041,"about_ca_system_score_codex":0.0028304725,"about_ca_system_score_gemma":0.004672803,"threshold_uncertainty_score":0.2356801},"labels":[],"label_agreement":null},{"id":"W4226286160","doi":"10.1038/s41588-021-00973-1","title":"Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology","year":2021,"lang":"en","type":"review","venue":"Nature Genetics","topic":"Amyotrophic Lateral Sclerosis Research","field":"Medicine","cited_by":552,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"McGill University; Montreal Neurological Institute and Hospital","funders":"National Institute of Neurological Disorders and Stroke; Medical Research Council; Agence Nationale de la Recherche; Rosetrees Trust; Motor Neurone Disease Association; Parkinson's UK; National Institute for Health and Care Research; Wellcome Trust","keywords":"Biology; Genome-wide association study; Amyotrophic lateral sclerosis; Mendelian randomization; Expression quantitative trait loci; Locus (genetics); Genetics; Genetic association; Genetic architecture; Disease; Quantitative trait locus; Single-nucleotide polymorphism; Gene; Genotype; Genetic variants; Internal medicine; Medicine","score_opus":0.0559748828511237,"score_gpt":0.36660030472391364,"score_spread":0.31062542187278996,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4226286160","genre_codex":"review","genre_gemma":"review","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"review","genre_consensus":"review","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.00012203901,0.9990246,0.000118305936,0.00021478857,0.0000750503,0.0000025718323,0.000026548696,0.000007642504,0.0004083587],"genre_scores_gemma":[0.0008298756,0.9983708,0.00021656332,0.00015783965,0.00008577215,0.0000053929984,0.000064144086,0.0000019565555,0.0002676787],"study_design_codex":"design_other","study_design_gemma":"observational","domain_scores_codex":[0.9997651,0.00004618118,0.00004548867,0.000051144387,0.00007294207,0.000019108636],"domain_scores_gemma":[0.9994653,0.0003008901,0.00007158082,0.000013222205,0.00010545095,0.000043520056],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0008977229,0.00084694166,0.0016440582,0.0023716795,0.00014713375,0.000822134,0.0010263387,0.00090305647,0.0024407266],"category_scores_gemma":[0.0010562043,0.00023536483,0.0006057737,0.0026178004,0.00041695492,0.000770603,0.0006684746,0.0010656117,0.001481879],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00013534212,0.00002409608,0.00035504013,0.0113360295,0.00026071834,0.00016359243,0.000024505409,0.00020552948,0.0006084456,0.0015098375,0.013663654,0.97171324],"study_design_scores_gemma":[0.00010515675,0.00018205587,0.0073504634,0.010203298,0.0010939391,0.0031659945,0.00008854782,0.00023271692,0.00064485095,0.0043167444,0.97255975,0.00005643944],"about_ca_topic_score_codex":0.0011419512,"about_ca_topic_score_gemma":0.0020277866,"teacher_disagreement_score":0.0024407266,"about_ca_system_score_codex":0.0004653583,"about_ca_system_score_gemma":0.0009591413,"threshold_uncertainty_score":0.008165002},"labels":[],"label_agreement":null},{"id":"W4229010457","doi":"10.1038/s41588-022-01057-4","title":"Genetic architecture of 11 major psychiatric disorders at biobehavioral, functional genomic and molecular genetic levels of analysis","year":2022,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Genetic Associations and Epidemiology","field":"Biochemistry, Genetics and Molecular Biology","cited_by":323,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Dalhousie University","funders":"National Institute of Mental Health; National Institute on Aging; Medical Research Council; H. Lundbeck A/S; Horizon 2020 Framework Programme; Novo Nordisk Fonden; Lundbeckfonden; Jacobs Foundation; ZonMw; Eunice Kennedy Shriver National Institute of Child Health and Human Development; Aarhus Universitet; European Commission; Novo Nordisk; National Institute for Health and Care Research; National Institutes of Health; NIHR Biomedical Research Centre, Royal Marsden NHS Foundation Trust/Institute of Cancer Research; Nederlandse Organisatie voor Wetenschappelijk Onderzoek; Wellcome Trust; Fritz Thyssen Stiftung; South London and Maudsley NHS Foundation Trust; Deutsche Forschungsgemeinschaft; King's College London; UK Research and Innovation","keywords":"Genetic architecture; Biology; Genetics; Genome-wide association study; Genetic association; Psychiatric genetics; Gene; Schizophrenia (object-oriented programming); Psychology; Psychiatry; Single-nucleotide polymorphism; Phenotype; Genotype","score_opus":0.006317861469321294,"score_gpt":0.24277050819089252,"score_spread":0.23645264672157124,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4229010457","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99758625,0.00010364591,0.0017891304,0.00007253005,0.0000017061403,0.0000110069695,0.0001420347,0.00001415272,0.00027963775],"genre_scores_gemma":[0.99805593,0.000061021856,0.0016178206,0.00001695699,0.0000028163497,0.000010496041,0.0001391912,0.0000052842984,0.000090455],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9981129,0.0007744071,0.00012183895,0.00054775603,0.00027824126,0.00016494528],"domain_scores_gemma":[0.9979656,0.0007400695,0.0008268254,0.00018467415,0.00012313171,0.00015975145],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0012072386,0.00067266304,0.0004914796,0.0013877447,0.0005579508,0.0006079673,0.00037582678,0.00038904106,0.0020247253],"category_scores_gemma":[0.0033106788,0.00035385767,0.00097235956,0.0011841875,0.00086536654,0.00022251798,0.001097275,0.00058626843,0.00010583349],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00042822052,0.000054947097,0.9754941,0.000024533236,0.000534535,0.00039034866,0.00020904322,0.0016250272,0.011821192,0.00097646465,0.00009993129,0.008341626],"study_design_scores_gemma":[0.000026328824,0.00015588937,0.99070823,0.000015415279,0.0003346351,0.0007395035,0.00012770342,0.005016244,0.0012286172,0.0014841976,0.00014712133,0.000016175023],"about_ca_topic_score_codex":0.0065651196,"about_ca_topic_score_gemma":0.010222328,"teacher_disagreement_score":0.0065651196,"about_ca_system_score_codex":0.00051248155,"about_ca_system_score_gemma":0.0008512691,"threshold_uncertainty_score":0.013053834},"labels":[],"label_agreement":null},{"id":"W4229063515","doi":"10.1038/s41588-022-01056-5","title":"Prioritization of autoimmune disease-associated genetic variants that perturb regulatory element activity in T cells","year":2022,"lang":"en","type":"article","venue":"Nature Genetics","topic":"T-cell and B-cell Immunology","field":"Immunology and Microbiology","cited_by":65,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of British Columbia","funders":"National Institute of Allergy and Infectious Diseases; National Institute of Arthritis and Musculoskeletal and Skin Diseases; National Institute of Neurological Disorders and Stroke; National Human Genome Research Institute; Howard Hughes Medical Institute","keywords":"Biology; Allele; Chromatin; Genetics; Locus (genetics); Computational biology; Gene; Effector; Autoimmune disease; Transcriptome; Genome-wide association study; Gene expression; Immunology; Genotype; Single-nucleotide polymorphism; Antibody","score_opus":0.007450844494484447,"score_gpt":0.2148690230624606,"score_spread":0.20741817856797617,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4229063515","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.98706156,0.0007919504,0.008169618,0.00031690145,0.00014359,0.000089346024,0.0005380214,0.00033208547,0.002556962],"genre_scores_gemma":[0.9944384,0.00013904544,0.0041320724,0.0002697148,0.00003664493,0.000021233313,0.00024756065,0.00013827384,0.0005770885],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9990715,0.00028543742,0.00011672276,0.00021095425,0.00015792483,0.00015740728],"domain_scores_gemma":[0.999166,0.0003509873,0.00016054511,0.00007351882,0.00007042007,0.00017858339],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0006936272,0.00068686233,0.0006846031,0.0011411639,0.00038850657,0.00071247277,0.00054819207,0.0009624542,0.005603241],"category_scores_gemma":[0.0010876765,0.00021634305,0.000491049,0.0004430683,0.00043129138,0.00021270433,0.0004267099,0.0010150819,0.0007581161],"study_design_candidate":"bench_or_experimental","study_design_consensus":"bench_or_experimental","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.001168623,0.00024746213,0.008511186,0.000079196296,0.00016406442,0.0008992146,0.000051512638,0.0011117773,0.97301435,0.00085381477,0.00038162296,0.01351729],"study_design_scores_gemma":[0.00093653466,0.003250632,0.112408645,0.0001867483,0.0019472132,0.01698603,0.0004874444,0.025318787,0.8175059,0.0032714282,0.017547663,0.00015291906],"about_ca_topic_score_codex":0.00071656966,"about_ca_topic_score_gemma":0.0023395526,"teacher_disagreement_score":0.005603241,"about_ca_system_score_codex":0.00024584812,"about_ca_system_score_gemma":0.0004121187,"threshold_uncertainty_score":0.018744767},"labels":[],"label_agreement":null},{"id":"W4230001841","doi":"10.1038/s41588-019-0565-x","title":"Author Correction: Postzygotic inactivating mutations of RHOA cause a mosaic neuroectodermal syndrome","year":2020,"lang":"en","type":"erratum","venue":"Nature Genetics","topic":"Ubiquitin and proteasome pathways","field":"Biochemistry, Genetics and Molecular Biology","cited_by":0,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"McGill Genome Centre; McGill University; Montreal Children's Hospital; McGill University Health Centre","funders":"","keywords":"Biology; RHOA; Genetics; Mosaic; Mutation; Gene; Signal transduction","score_opus":0.014855345951491898,"score_gpt":0.2698588783907263,"score_spread":0.2550035324392344,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4230001841","genre_codex":"editorial","genre_gemma":"other","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"other","genre_consensus":null,"domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.00029183412,0.00070062804,0.0006214595,0.027440352,0.9685497,0.00001415437,0.00043038497,0.00023513308,0.00171639],"genre_scores_gemma":[0.037422154,0.010167187,0.009414829,0.086399354,0.55491906,0.00020789873,0.0024163052,0.002514487,0.29653868],"study_design_codex":"not_applicable","study_design_gemma":"not_applicable","domain_scores_codex":[0.99781126,0.00026431686,0.00038818136,0.00033734465,0.0009728845,0.00022611172],"domain_scores_gemma":[0.9876397,0.0034647167,0.00075636496,0.0007148152,0.006480512,0.00094380905],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.002061201,0.0022810965,0.0017685016,0.003029217,0.0026355945,0.002689039,0.0035561332,0.0088259345,0.030736372],"category_scores_gemma":[0.028878715,0.0012163445,0.0015271577,0.0013114741,0.0018433286,0.0015605264,0.001299089,0.009953415,0.017227408],"study_design_candidate":"not_applicable","study_design_consensus":"not_applicable","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00005799129,0.000011118177,0.000109318426,0.00012092568,0.000027496793,0.0035819362,0.000034853143,0.000077244666,0.00017076869,0.00086106895,0.98944354,0.005503759],"study_design_scores_gemma":[0.00010824614,0.000037350223,0.0010019145,0.00025939895,0.00010427278,0.008490278,0.00008625058,0.0004840725,0.0011423241,0.0017006414,0.98651785,0.00006736614],"about_ca_topic_score_codex":0.009835809,"about_ca_topic_score_gemma":0.012632012,"teacher_disagreement_score":0.030736372,"about_ca_system_score_codex":0.002723686,"about_ca_system_score_gemma":0.002741153,"threshold_uncertainty_score":0.10282338},"labels":[],"label_agreement":null},{"id":"W4239337183","doi":"10.1038/87298","title":"A detailed transcript map of the human chromosome 12p12.3 tumor suppressor locus: the usefulness of an integrative approach","year":2001,"lang":"en","type":"article","venue":"Nature Genetics","topic":"RNA modifications and cancer","field":"Biochemistry, Genetics and Molecular Biology","cited_by":0,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Centre Hospitalier Universitaire Sainte-Justine","funders":"","keywords":"Biology; Locus (genetics); Suppressor; Genetics; Computational biology; Chromosome; Gene","score_opus":0.013184354371981021,"score_gpt":0.25643460821587194,"score_spread":0.24325025384389093,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4239337183","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.7286487,0.008526926,0.23235662,0.001387819,0.00029153907,0.0004406126,0.013521955,0.0025246562,0.012301137],"genre_scores_gemma":[0.79277617,0.009467348,0.1419087,0.00037165757,0.00019809886,0.00035840637,0.03963455,0.0006223404,0.01466275],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9999305,0.0000052794203,0.0000040813165,0.000024467123,0.000021184065,0.000014486976],"domain_scores_gemma":[0.9999287,0.000018518122,0.000010295009,0.000010492427,0.0000135432765,0.000018393086],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.000108750486,0.00048403867,0.0004314978,0.000625156,0.00041011247,0.00039936134,0.00031541826,0.000352425,0.0025293566],"category_scores_gemma":[0.00012399328,0.00034710663,0.0005977899,0.0004984463,0.00022931116,0.00024573543,0.00022648596,0.0009489161,0.0017136061],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.000106037674,0.000012452329,0.0000731225,0.00006749929,0.000003849698,0.00015110166,0.000023930566,0.00022105125,0.9946682,0.00041739867,0.00013943201,0.0041160607],"study_design_scores_gemma":[0.00014259678,0.00058518053,0.023616597,0.000070426984,0.00016075332,0.0021641154,0.00013569099,0.0028155767,0.9165829,0.0034279113,0.05024138,0.000056891946],"about_ca_topic_score_codex":0.0014928785,"about_ca_topic_score_gemma":0.0023812028,"teacher_disagreement_score":0.0025293566,"about_ca_system_score_codex":0.00028119073,"about_ca_system_score_gemma":0.00049758446,"threshold_uncertainty_score":0.008461535},"labels":[],"label_agreement":null},{"id":"W4239490150","doi":"10.1038/s41588-018-0082-3","title":"Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity","year":2018,"lang":"en","type":"erratum","venue":"Nature Genetics","topic":"Adipose Tissue and Metabolism","field":"Medicine","cited_by":11,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"York University; Université de Montréal; Dalhousie University; Montreal Heart Institute","funders":"National Cancer Institute; Medical Research Council; National Institute for Health and Care Research; Steno Diabetes Center Copenhagen; European Hematology Association","keywords":"Biostatistics; Body mass index; Biology; Index (typography); Obesity; Epidemiology; Gerontology; Library science; Medicine; Internal medicine; Endocrinology; Computer science","score_opus":0.010490916322781851,"score_gpt":0.23405326238362179,"score_spread":0.22356234606083994,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4239490150","genre_codex":"editorial","genre_gemma":"other","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"other","genre_consensus":null,"domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.00013987343,0.00069830084,0.00045239239,0.0308333,0.96550757,0.000011091084,0.0005244609,0.00017961048,0.0016534054],"genre_scores_gemma":[0.019037427,0.0077293348,0.006849127,0.089248195,0.55418473,0.00022222883,0.0030147599,0.0021528471,0.31756133],"study_design_codex":"not_applicable","study_design_gemma":"not_applicable","domain_scores_codex":[0.9964393,0.0005353966,0.00061611825,0.000527541,0.0015337135,0.00034789808],"domain_scores_gemma":[0.97457933,0.0069407513,0.0014164872,0.0016019216,0.014308175,0.0011534006],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0037243313,0.0021793914,0.0019973028,0.003619365,0.0028626472,0.0037910182,0.0035056702,0.0070981593,0.05296892],"category_scores_gemma":[0.04944075,0.001280859,0.0018805178,0.0018585294,0.0019847522,0.0018526184,0.0017762706,0.012511792,0.023948098],"study_design_candidate":"not_applicable","study_design_consensus":"not_applicable","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.000034055287,0.000005530664,0.00010131615,0.00009289431,0.00001802768,0.0006989855,0.000021538379,0.000043284985,0.00004574414,0.00045475634,0.99383175,0.004652104],"study_design_scores_gemma":[0.00007193418,0.00002412855,0.0009265978,0.00037484308,0.00009524316,0.0018645606,0.000077743585,0.00035316142,0.0004531723,0.001408538,0.99430734,0.000042691965],"about_ca_topic_score_codex":0.01366792,"about_ca_topic_score_gemma":0.01991654,"teacher_disagreement_score":0.05296892,"about_ca_system_score_codex":0.0036151765,"about_ca_system_score_gemma":0.0042590154,"threshold_uncertainty_score":0.17719871},"labels":[],"label_agreement":null},{"id":"W4246697467","doi":"10.1038/ng765","title":"MLL translocations specify a distinct gene expression profile that distinguishes a unique leukemia","year":2001,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Acute Myeloid Leukemia Research","field":"Medicine","cited_by":1719,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Princess Margaret Cancer Centre; University of Toronto","funders":"Bristol-Myers Squibb; American Society of Hematology","keywords":"Biology; Chromosomal translocation; Leukemia; Hox gene; Gene; Haematopoiesis; Genetics; Cancer research; Gene expression; Stem cell","score_opus":0.025728755683725048,"score_gpt":0.31144017925646067,"score_spread":0.2857114235727356,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4246697467","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9949386,0.0005056575,0.0018333581,0.00016411082,0.000016196354,0.000016832151,0.00069990347,0.000093827155,0.0017313675],"genre_scores_gemma":[0.9959337,0.00030961298,0.0012079867,0.0001062667,0.000021766708,0.00002380699,0.001083865,0.000040344483,0.0012727855],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9997615,0.000021484831,0.00001914914,0.000052102223,0.000062427214,0.00008322331],"domain_scores_gemma":[0.9997484,0.00006983042,0.00007076301,0.00003017172,0.00002523763,0.000055515036],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0001626641,0.000250856,0.00026491034,0.0007539026,0.0002609367,0.00080320105,0.00014157691,0.00037927373,0.0016635893],"category_scores_gemma":[0.0003137211,0.000252061,0.00017791826,0.000395549,0.00039288378,0.0004231306,0.0004961534,0.0007929017,0.0009136434],"study_design_candidate":"bench_or_experimental","study_design_consensus":"bench_or_experimental","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00022187625,0.000017970357,0.0030746048,0.000011662196,0.0000053221383,0.00015111684,0.000056506808,0.0000515637,0.99352986,0.00055221573,0.00008710619,0.0022402322],"study_design_scores_gemma":[0.0001379617,0.0005851253,0.18818043,0.000022424969,0.00009029733,0.0071295407,0.00083480607,0.0014620665,0.78904146,0.0019223386,0.010558847,0.000034700854],"about_ca_topic_score_codex":0.00021120864,"about_ca_topic_score_gemma":0.00058731285,"teacher_disagreement_score":0.0016635893,"about_ca_system_score_codex":0.00048198176,"about_ca_system_score_gemma":0.00016319419,"threshold_uncertainty_score":0.0055652857},"labels":[],"label_agreement":null},{"id":"W4280552086","doi":"10.1038/s41588-022-01058-3","title":"Multi-ancestry genetic study of type 2 diabetes highlights the power of diverse populations for discovery and translation","year":2022,"lang":"en","type":"review","venue":"Nature Genetics","topic":"Genetic Associations and Epidemiology","field":"Biochemistry, Genetics and Molecular Biology","cited_by":739,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"McGill University; Impact; Hamilton Health Sciences; University of Toronto; McMaster University; Population Health Research Institute","funders":"National Heart, Lung, and Blood Institute; National Center for Advancing Translational Sciences; Medical Research Council; Genentech; National Cancer Institute; Servier; Shionogi; Novo Nordisk Fonden; Novo Nordisk; Vertex Pharmaceuticals; Steno Diabetes Center Copenhagen; Wellcome Trust; National Institutes of Health; Regeneron Pharmaceuticals; Respicardia; Harvard University; U.S. Department of Health and Human Services; Kowa Company; National Institute of Diabetes and Digestive and Kidney Diseases; Sanofi; National Institute on Aging; National Institute for Health and Care Research; Massachusetts General Hospital; GlaxoSmithKline; Guangdong Provincial People's Hospital; Eli Lilly and Company; Bristol-Myers Squibb; AstraZeneca; Amgen; Pfizer; Steno Diabetes Center Aarhus; McMaster University; Yale University","keywords":"Biology; Type 2 diabetes; Translation (biology); Genetics; Computational biology; Evolutionary biology; Type (biology); Genetic genealogy; Diabetes mellitus; Demography; Population; Gene; Sociology; Endocrinology; Ecology","score_opus":0.06833353806244687,"score_gpt":0.3585684173584159,"score_spread":0.29023487929596903,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4280552086","genre_codex":"review","genre_gemma":"review","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"review","genre_consensus":"review","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.00004036463,0.9977223,0.00025333374,0.0011851684,0.0004758618,0.000002237377,0.000024186082,0.0000063526427,0.0002901263],"genre_scores_gemma":[0.00033016084,0.99769247,0.0002938612,0.00078334,0.00067061494,0.000005219707,0.00002845384,0.000002051065,0.00019381427],"study_design_codex":"design_other","study_design_gemma":"observational","domain_scores_codex":[0.9994404,0.00017305904,0.00006590668,0.00010532128,0.00017493678,0.000040402756],"domain_scores_gemma":[0.99630356,0.002757192,0.00015264498,0.00009153603,0.00053323375,0.00016186906],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0033643222,0.001158718,0.00225139,0.0020839968,0.0002892703,0.0014630919,0.0013846825,0.0021787458,0.0024204324],"category_scores_gemma":[0.004260421,0.0003562844,0.000763572,0.0023381228,0.0011958953,0.0015921306,0.0012884506,0.0038997096,0.0012367882],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00015683279,0.000042633706,0.00063233584,0.009364299,0.00032392732,0.00020587168,0.000044782595,0.00033603125,0.00053437304,0.009636593,0.05032809,0.9283942],"study_design_scores_gemma":[0.00007499658,0.00008768314,0.0025696913,0.0082397135,0.00046577782,0.0009256038,0.00008842421,0.00016646717,0.00021208164,0.013740113,0.9733811,0.000048318467],"about_ca_topic_score_codex":0.0028568003,"about_ca_topic_score_gemma":0.0047680144,"teacher_disagreement_score":0.0033643222,"about_ca_system_score_codex":0.0011442634,"about_ca_system_score_gemma":0.0020736875,"threshold_uncertainty_score":0.017792463},"labels":[],"label_agreement":null},{"id":"W4282919870","doi":"10.1038/s41588-022-01093-0","title":"One step closer to linking GWAS SNPs with the right genes","year":2022,"lang":"en","type":"letter","venue":"Nature Genetics","topic":"Genetic Associations and Epidemiology","field":"Biochemistry, Genetics and Molecular Biology","cited_by":4,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Université de Montréal; Montreal Heart Institute","funders":"","keywords":"Biology; Gene; Single-nucleotide polymorphism; Genome-wide association study; Phenotype; Genetics; Computational biology; Genetic architecture; Human genome; Genome; Genotype","score_opus":0.008585394018454666,"score_gpt":0.24734907662162628,"score_spread":0.2387636826031716,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4282919870","genre_codex":"commentary","genre_gemma":"commentary","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"commentary","genre_consensus":"commentary","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.00040744388,0.00072072877,0.00041412766,0.97897583,0.01865827,0.0000068306595,0.000043621705,0.000022012073,0.00075107644],"genre_scores_gemma":[0.005472834,0.00064564083,0.0010039698,0.91264564,0.077137604,0.000029738134,0.00002868203,0.000026005333,0.0030098567],"study_design_codex":"not_applicable","study_design_gemma":"not_applicable","domain_scores_codex":[0.99467635,0.0020680262,0.00057175313,0.00092918705,0.0012854909,0.00046918346],"domain_scores_gemma":[0.96748054,0.023187742,0.0011167163,0.0014623989,0.0034300892,0.003322422],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.009066525,0.00091681804,0.0024633151,0.0009125594,0.0036593282,0.004835058,0.0021909967,0.043752488,0.005950635],"category_scores_gemma":[0.042634606,0.00087307434,0.0012455336,0.0005531381,0.0050529167,0.0053170654,0.0020152798,0.06776471,0.0044683143],"study_design_candidate":"not_applicable","study_design_consensus":"not_applicable","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0003720819,0.00016100341,0.0033862763,0.000110509754,0.00016507477,0.0031938504,0.0003893932,0.0002431965,0.00088413665,0.015392899,0.9503472,0.02535442],"study_design_scores_gemma":[0.0013407492,0.0003629024,0.0071037766,0.00056194427,0.0002335087,0.0071328892,0.0014698368,0.003124112,0.0014984336,0.21191463,0.7649206,0.00033665617],"about_ca_topic_score_codex":0.003736313,"about_ca_topic_score_gemma":0.004878292,"teacher_disagreement_score":0.043752488,"about_ca_system_score_codex":0.0025533594,"about_ca_system_score_gemma":0.002591503,"threshold_uncertainty_score":0.047948897},"labels":[],"label_agreement":null},{"id":"W4285006295","doi":"10.1038/s41588-022-01102-2","title":"A sequence-based global map of regulatory activity for deciphering human genetics","year":2022,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Genomics and Chromatin Dynamics","field":"Biochemistry, Genetics and Molecular Biology","cited_by":275,"is_retracted":false,"has_abstract":true,"route_ca_aff":false,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"","funders":"National Institute of General Medical Sciences; National Human Genome Research Institute; Flatiron Health; Simons Foundation; University of Texas Southwestern Medical Center; Canadian Institute for Advanced Research; National Heart, Lung, and Blood Institute; Princeton University; National Institute of Allergy and Infectious Diseases; Cancer Prevention and Research Institute of Texas; National Institutes of Health; U.S. Department of Health and Human Services; National Science Foundation","keywords":"Biology; Regulatory sequence; Computational biology; Epigenomics; Genetics; Chromatin; Sequence (biology); Enhancer; Regulation of gene expression; Gene; Transcription factor; Gene expression; DNA methylation","score_opus":0.010367420595507673,"score_gpt":0.2700728022538486,"score_spread":0.25970538165834095,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4285006295","genre_codex":"methods","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":null,"domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.20403774,0.003532673,0.772989,0.00045334556,0.000035567402,0.000040684652,0.010656925,0.0024542364,0.005799847],"genre_scores_gemma":[0.84619546,0.0021610733,0.1417603,0.0001807568,0.000054178454,0.00009422155,0.007286229,0.00034177498,0.0019260905],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9998523,0.000025023754,0.0000059309905,0.00007959209,0.000025344576,0.0000117120235],"domain_scores_gemma":[0.9996105,0.00018424736,0.00006170707,0.00007692778,0.000034518405,0.000032114975],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00039944015,0.00041006654,0.00042340238,0.0014688413,0.00022656869,0.0005479379,0.00037492195,0.0003795846,0.0025017823],"category_scores_gemma":[0.0011174988,0.00029288488,0.00048500067,0.0011928021,0.0005357241,0.0008773851,0.0005500852,0.00081860804,0.0005993893],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.000605629,0.00013469315,0.06507797,0.0006490638,0.00031694715,0.00017697872,0.00036339415,0.16678463,0.35606202,0.07127922,0.0052679083,0.33328155],"study_design_scores_gemma":[0.00004925482,0.00029087366,0.06102099,0.00014622476,0.0002147578,0.0004311299,0.00016527252,0.61281854,0.06678411,0.22707848,0.030909188,0.00009112925],"about_ca_topic_score_codex":0.002465267,"about_ca_topic_score_gemma":0.004725724,"teacher_disagreement_score":0.0025017823,"about_ca_system_score_codex":0.00042003332,"about_ca_system_score_gemma":0.0004555729,"threshold_uncertainty_score":0.008369327},"labels":[],"label_agreement":null},{"id":"W4285391095","doi":"10.1038/s41588-022-01113-z","title":"Genetic regulation of OAS1 nonsense-mediated decay underlies association with COVID-19 hospitalization in patients of European and African ancestries","year":2022,"lang":"en","type":"article","venue":"Nature Genetics","topic":"interferon and immune responses","field":"Immunology and Microbiology","cited_by":138,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Toronto; Toronto General Hospital; University Health Network","funders":"Division of Cancer Epidemiology and Genetics, National Cancer Institute; National Center for Advancing Translational Sciences; National Institute of Neurological Disorders and Stroke; National Institute of Allergy and Infectious Diseases; National Institute of General Medical Sciences; Oxford Nanopore Technologies; Weill Cornell Medical College; National Institute on Aging; Center for Clinical and Translational Science, University of Alabama at Birmingham; Emory Medical Care Foundation; Deutsche Forschungsgemeinschaft; Massachusetts Consortium on Pathogen Readiness; National Human Genome Research Institute; Hellenic Foundation for Research and Innovation; Universidade de São Paulo; European Commission; Seoul National University Bundang Hospital; Wayne and Gladys Valley Foundation; University of Alabama at Birmingham; Kaiser Permanente; University of Alabama; National Cancer Institute; U.S. Department of Health and Human Services; Genomic Health; Emory University; Frederick National Laboratory for Cancer Research; National Institutes of Health; Robert Wood Johnson Foundation; Ellison Medical Foundation","keywords":"Biology; Haplotype; Locus (genetics); Allele; Genetics; Genome-wide association study; Single-nucleotide polymorphism; Nonsense-mediated decay; Disease; Gene; RNA splicing; Genotype; Medicine; RNA; Internal medicine","score_opus":0.006092664110982121,"score_gpt":0.21982983738184025,"score_spread":0.21373717327085814,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4285391095","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9994331,0.00008537571,0.00022310477,0.000026856922,0.000004271941,0.0000024194198,0.00008612849,0.0000031799884,0.00013548724],"genre_scores_gemma":[0.99958795,0.00002602063,0.00014790669,0.000013718749,0.000005153891,0.000002439746,0.00010036886,0.0000033242368,0.0001130413],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9997603,0.000060494,0.000029921523,0.000088755296,0.000024049179,0.000036442125],"domain_scores_gemma":[0.9996086,0.000096924734,0.00018186409,0.00003280897,0.000018319355,0.00006157885],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00024543382,0.0002960243,0.0002530005,0.00044243984,0.00028272084,0.00027767094,0.00016760734,0.00031433936,0.0032773959],"category_scores_gemma":[0.00073727896,0.000110186505,0.00040696785,0.00041032463,0.00023724612,0.00011694086,0.0002059259,0.00032206907,0.00019092108],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0016255317,0.00007616294,0.94425625,0.000029124976,0.00023017847,0.001074933,0.00022610433,0.0001443228,0.045878235,0.00020811596,0.0001830174,0.00606806],"study_design_scores_gemma":[0.000029545834,0.00019345288,0.994622,0.000008709287,0.00008809348,0.002011652,0.00013406991,0.0006203511,0.0018127112,0.00014217195,0.000330496,0.0000067051647],"about_ca_topic_score_codex":0.0008857568,"about_ca_topic_score_gemma":0.0008825626,"teacher_disagreement_score":0.0032773959,"about_ca_system_score_codex":0.00010984514,"about_ca_system_score_gemma":0.00010114642,"threshold_uncertainty_score":0.010963976},"labels":[],"label_agreement":null},{"id":"W4285727773","doi":"10.1038/s41588-022-01127-7","title":"Reference genome assemblies reveal the origin and evolution of allohexaploid oat","year":2022,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Chromosomal and Genetic Variations","field":"Agricultural and Biological Sciences","cited_by":179,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Institute of Genetics","funders":"University of California, Davis; Genome Center, University of California, Davis; Fundamental Research Funds for the Central Universities; People's Government of Jilin Province; Sichuan Agricultural University; National Natural Science Foundation of China; Brigham Young University","keywords":"Biology; Genome; Polyploid; Avena; Sequence assembly; Contig; Reference genome; Synteny; Ploidy; Crop; Genetics; Computational biology; Evolutionary biology; Transcriptome; Botany; Gene; Agronomy","score_opus":0.018962056163537234,"score_gpt":0.23391462146359587,"score_spread":0.21495256530005863,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4285727773","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.91279846,0.005483746,0.048915036,0.00032589454,0.00016807849,0.00006397861,0.025724877,0.0018097104,0.0047101057],"genre_scores_gemma":[0.8124671,0.003957775,0.06560379,0.00021203475,0.00004428332,0.00008662979,0.11224402,0.0009237304,0.0044605574],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99952555,0.000042500047,0.00006155061,0.0002252304,0.00009911702,0.00004605516],"domain_scores_gemma":[0.9992607,0.0001420482,0.00014206351,0.00015237223,0.00023058635,0.00007209721],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0007860666,0.00055873656,0.0003796255,0.0011359364,0.00050477457,0.00106768,0.00041811855,0.00045528638,0.0010737859],"category_scores_gemma":[0.0016887392,0.00030659424,0.0006266079,0.0017156393,0.00018067528,0.000693776,0.0005943519,0.000603676,0.0006057044],"study_design_candidate":"bench_or_experimental","study_design_consensus":"bench_or_experimental","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0006013962,0.000031924123,0.023459477,0.00046609528,0.00019744906,0.00055217545,0.0005965147,0.0029792176,0.9242117,0.0014418713,0.0014402097,0.044022046],"study_design_scores_gemma":[0.00010571801,0.000496756,0.4556917,0.00033109996,0.0010137099,0.0018123254,0.0010943344,0.028542621,0.34055036,0.0034939155,0.1666973,0.00017018228],"about_ca_topic_score_codex":0.004348877,"about_ca_topic_score_gemma":0.008940883,"teacher_disagreement_score":0.004348877,"about_ca_system_score_codex":0.0007027505,"about_ca_system_score_gemma":0.00053247664,"threshold_uncertainty_score":0.008647144},"labels":[],"label_agreement":null},{"id":"W4288447807","doi":"10.1038/s41588-022-01134-8","title":"Single-nucleus and spatial transcriptome profiling of pancreatic cancer identifies multicellular dynamics associated with neoadjuvant treatment","year":2022,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Pancreatic and Hepatic Oncology Research","field":"Medicine","cited_by":413,"is_retracted":false,"has_abstract":false,"route_ca_aff":false,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"","funders":"Moonshot Research and Development Program; National Cancer Institute; Stand Up To Cancer; University of California, San Francisco; Klarman Cell Observatory, Broad Institute; National Science Foundation; Damon Runyon Cancer Research Foundation; Pancreatic Cancer Canada Foundation; Princess Margaret Cancer Foundation; Ludwig Institute for Cancer Research; Canadian Cancer Society Research Institute; Schweizerischer Nationalfonds zur Förderung der Wissenschaftlichen Forschung; National Institute of Diabetes and Digestive and Kidney Diseases; Lustgarten Foundation; Conquer Cancer Foundation; Government of Ontario; Howard Hughes Medical Institute","keywords":"Biology; Transcriptome; Pancreatic cancer; Multicellular organism; Cancer research; Progenitor cell; Gene expression profiling; Computational biology; Phenotype; Bioinformatics; Cell; Cancer; Stem cell; Genetics; Gene expression; Gene","score_opus":0.020933303459506006,"score_gpt":0.3036530425954979,"score_spread":0.2827197391359919,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4288447807","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9953975,0.0008389936,0.0019344094,0.00010976407,0.000014370861,0.000006821138,0.0007071936,0.000051170395,0.00093977153],"genre_scores_gemma":[0.997489,0.00033113934,0.000883237,0.00004446621,0.0000058334654,0.00001635493,0.0004978211,0.00002049772,0.000711665],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9998783,0.000013618696,0.0000046652976,0.000039198938,0.000033502518,0.000030781513],"domain_scores_gemma":[0.99987626,0.000026499436,0.000038990263,0.000013470999,0.000021716834,0.00002313494],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00010425726,0.00009124612,0.00028679118,0.00021208708,0.0001915288,0.00053163123,0.00010536665,0.00019373135,0.0010354602],"category_scores_gemma":[0.0002747369,0.00014967247,0.0001942252,0.000323887,0.00019167988,0.00031895324,0.000228221,0.00032379685,0.00025729867],"study_design_candidate":"bench_or_experimental","study_design_consensus":"bench_or_experimental","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00046719296,0.000026410376,0.021155009,0.00007295193,0.000033669712,0.000073004616,0.00014937975,0.0006528994,0.96869206,0.00021066022,0.0004103734,0.008056247],"study_design_scores_gemma":[0.00001576972,0.00023216833,0.7804766,0.000019854726,0.00006841018,0.0004040085,0.0009623775,0.012069982,0.2012421,0.00047937816,0.0039994516,0.000029952624],"about_ca_topic_score_codex":0.0012847051,"about_ca_topic_score_gemma":0.0028345936,"teacher_disagreement_score":0.0012847051,"about_ca_system_score_codex":0.000386708,"about_ca_system_score_gemma":0.00021058487,"threshold_uncertainty_score":0.003463924},"labels":[],"label_agreement":null},{"id":"W4289260965","doi":"10.1038/s41588-022-01115-x","title":"Cross-ancestry genome-wide meta-analysis of 61,047 cases and 947,237 controls identifies new susceptibility loci contributing to lung cancer","year":2022,"lang":"en","type":"review","venue":"Nature Genetics","topic":"Genetic Associations and Epidemiology","field":"Biochemistry, Genetics and Molecular Biology","cited_by":121,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Sinai Health System; Public Health Ontario; Lunenfeld-Tanenbaum Research Institute; University of Toronto; University Health Network; Princess Margaret Cancer Centre; Université Laval; Institut universitaire de cardiologie et de pneumologie de Québec","funders":"Division of Cancer Epidemiology and Genetics, National Cancer Institute; National Center for Research Resources; National Institute of Environmental Health Sciences; National Heart, Lung, and Blood Institute; National Institute on Aging; Cancer Research UK; Sheffield Hospitals Charity; Kaiser Permanente; National Cancer Institute; National Institutes of Health; U.S. Department of Health and Human Services; Cancer Prevention and Research Institute of Texas; National Human Genome Research Institute; World Health Organization","keywords":"Biology; Genetics; Genome; Genome-wide association study; Lung cancer; Cancer; Computational biology; Single-nucleotide polymorphism; Gene; Oncology; Genotype","score_opus":0.06891846769585076,"score_gpt":0.4107296997289847,"score_spread":0.34181123203313396,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4289260965","genre_codex":"review","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":null,"domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.0009862158,0.9973137,0.0005234956,0.00037959457,0.00014439537,0.0000069010994,0.0002881312,0.000013882005,0.00034366877],"genre_scores_gemma":[0.008654174,0.98853403,0.0010769857,0.00040767383,0.0003482308,0.000019675275,0.00058873004,0.000008727837,0.00036164065],"study_design_codex":"design_other","study_design_gemma":"meta_analysis","domain_scores_codex":[0.9994106,0.00018404353,0.00008871985,0.00015908846,0.000117679956,0.000039833194],"domain_scores_gemma":[0.99864274,0.00096935354,0.00013971455,0.0000733771,0.000129635,0.00004516775],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0023471876,0.0012534568,0.0028785453,0.0015119812,0.0001417298,0.0009431689,0.0010112604,0.0009537343,0.001951069],"category_scores_gemma":[0.0025667641,0.00043392304,0.0021789654,0.0028163118,0.00023599603,0.00044119594,0.00065610174,0.0010881983,0.0005228504],"study_design_candidate":"meta_analysis","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0013227005,0.000072111216,0.020628158,0.033320054,0.023848964,0.00058154465,0.00006043452,0.0006852529,0.0017190953,0.0014722287,0.022976736,0.89331275],"study_design_scores_gemma":[0.0012993048,0.00088831043,0.20606792,0.024450192,0.13310991,0.005946033,0.000284447,0.001228156,0.0032110754,0.012708259,0.6105156,0.00029078522],"about_ca_topic_score_codex":0.002885232,"about_ca_topic_score_gemma":0.0072503397,"teacher_disagreement_score":0.002885232,"about_ca_system_score_codex":0.00041169734,"about_ca_system_score_gemma":0.0011104424,"threshold_uncertainty_score":0.012413263},"labels":[],"label_agreement":null},{"id":"W4293068820","doi":"10.1038/s41588-022-01104-0","title":"Rare coding variation provides insight into the genetic architecture and phenotypic context of autism","year":2022,"lang":"en","type":"review","venue":"Nature Genetics","topic":"Autism Spectrum Disorder Research","field":"Neuroscience","cited_by":617,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Hospital for Sick Children","funders":"National Institute of Environmental Health Sciences; National Human Genome Research Institute; Simons Foundation; Eunice Kennedy Shriver National Institute of Child Health and Human Development; Autism Speaks; National Institute of Mental Health; U.S. Department of Health and Human Services; National Science Foundation","keywords":"Biology; Genetic architecture; Phenotype; Variation (astronomy); Autism; Genetics; Coding (social sciences); Context (archaeology); Genetic variation; Computational biology; Evolutionary biology; Gene; Developmental psychology","score_opus":0.03548041740004735,"score_gpt":0.31520132780340493,"score_spread":0.27972091040335756,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4293068820","genre_codex":"review","genre_gemma":"review","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"review","genre_consensus":"review","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.0000972909,0.9976884,0.00037657315,0.00060144725,0.0003660204,0.000002064535,0.00003105582,0.000009995763,0.0008272471],"genre_scores_gemma":[0.00067506183,0.9975394,0.0003532402,0.0003355124,0.000548763,0.0000034847235,0.00005347688,0.0000026875132,0.00048839767],"study_design_codex":"design_other","study_design_gemma":"observational","domain_scores_codex":[0.9997547,0.000040462593,0.000035993635,0.000063986845,0.000085950625,0.000018940973],"domain_scores_gemma":[0.9993247,0.0004271462,0.00006123995,0.00002049379,0.00011831021,0.00004822455],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0009216597,0.001073519,0.0014144253,0.0019364734,0.0001755826,0.00097506377,0.0011905817,0.0013470043,0.002368588],"category_scores_gemma":[0.0013795537,0.00026623765,0.00042773783,0.0016698971,0.0008152517,0.0010440546,0.00075179944,0.0020616946,0.0012327554],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00008697895,0.000021668227,0.0003799454,0.005207318,0.00014026136,0.00052845967,0.000030314357,0.00055281515,0.0022711304,0.007961814,0.036053136,0.9467662],"study_design_scores_gemma":[0.000028388089,0.00005536639,0.0017491163,0.00317808,0.00025178184,0.0034866568,0.00005393806,0.00020042332,0.0005774198,0.008416815,0.98196167,0.000040378174],"about_ca_topic_score_codex":0.0015991223,"about_ca_topic_score_gemma":0.0028548397,"teacher_disagreement_score":0.002368588,"about_ca_system_score_codex":0.00080631714,"about_ca_system_score_gemma":0.001293416,"threshold_uncertainty_score":0.007923782},"labels":[],"label_agreement":null},{"id":"W4293475192","doi":"10.1038/s41588-022-01156-2","title":"Large-scale sequencing identifies multiple genes and rare variants associated with Crohn’s disease susceptibility","year":2022,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Inflammatory Bowel Disease","field":"Biochemistry, Genetics and Molecular Biology","cited_by":189,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Université de Montréal; McMaster University; University of Manitoba; Montreal Heart Institute; McGill University Health Centre; Mount Sinai Hospital","funders":"National Institute on Aging; Medical Research Council; National Institute of Diabetes and Digestive and Kidney Diseases; Stanley Center for Psychiatric Research, Broad Institute; NIHR Newcastle Biomedical Research Centre; Crohn's and Colitis UK; Fonds De La Recherche Scientifique - FNRS; Academy of Finland; Leona M. and Harry B. Helmsley Charitable Trust; National Institute for Health and Care Research; Broad Institute; National Human Genome Research Institute; NIHR Oxford Biomedical Research Centre; Wellcome Trust; National Institutes of Health; U.S. Department of Health and Human Services","keywords":"Biology; Genetics; Gene; Computational biology; Disease; Crohn's disease","score_opus":0.006427685364769132,"score_gpt":0.22715928082067585,"score_spread":0.22073159545590673,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4293475192","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9930062,0.00089480216,0.0031710987,0.000408602,0.00008836233,0.000021005815,0.0010932498,0.00008352783,0.00123312],"genre_scores_gemma":[0.9964194,0.00024404791,0.0020098924,0.00019401737,0.0000763033,0.000011366314,0.0006312731,0.000039826693,0.00037388928],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9993437,0.00013438328,0.000069284644,0.00020802935,0.00017335414,0.0000712472],"domain_scores_gemma":[0.99836177,0.00096702203,0.00029435102,0.0001038716,0.000078723635,0.00019431548],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0005124574,0.00074998336,0.00064001407,0.0016334358,0.0005412112,0.00095015764,0.0004613118,0.001333476,0.0019906766],"category_scores_gemma":[0.0022034433,0.00030389393,0.0008137965,0.0010146004,0.0005323325,0.0001984147,0.00041880007,0.00085435784,0.00034274897],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0035369217,0.00029307505,0.4428147,0.00029034482,0.0018514339,0.03196362,0.0009169861,0.00294442,0.46193182,0.0022308757,0.0028915994,0.048334163],"study_design_scores_gemma":[0.0003432124,0.00039475784,0.9279095,0.00013952648,0.0013973882,0.02798365,0.00037224064,0.00568373,0.025274124,0.003017426,0.007401276,0.00008323105],"about_ca_topic_score_codex":0.0013321642,"about_ca_topic_score_gemma":0.0029476366,"teacher_disagreement_score":0.0019906766,"about_ca_system_score_codex":0.0002404399,"about_ca_system_score_gemma":0.00023603161,"threshold_uncertainty_score":0.006659448},"labels":[],"label_agreement":null},{"id":"W4294904260","doi":"10.1038/s41588-022-01165-1","title":"Genome-wide association analyses of physical activity and sedentary behavior provide insights into underlying mechanisms and roles in disease prevention","year":2022,"lang":"en","type":"review","venue":"Nature Genetics","topic":"Genetic Associations and Epidemiology","field":"Biochemistry, Genetics and Molecular Biology","cited_by":236,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Impact; Université Laval; McMaster University","funders":"National Institute of Neurological Disorders and Stroke; National Institute of Diabetes and Digestive and Kidney Diseases; National Human Genome Research Institute; National Heart, Lung, and Blood Institute; National Institute on Aging; Helmholtz Zentrum München; Statens Serum Institut; Feinberg School of Medicine; National Institutes of Health; Novo Nordisk Foundation Center for Basic Metabolic Research; Medical Research Council; Uppsala Universitet; Tartu Ülikool; Technische Universität München; British Heart Foundation; China Scholarship Council; Vetenskapsrådet; National Cancer Institute; University College London; Université de Lausanne; Karolinska Institutet; Seoul National University; Northwestern University; Genome Institute of Singapore; National Research Foundation of Korea; Ministry of Science, ICT and Future Planning; Novo Nordisk; Universität Greifswald; Hjärt-Lungfonden; Agency for Science, Technology and Research; University of Surrey; National Institute for Health and Care Research; National Research Foundation; University of Bristol; Wellcome Trust; Cancer Research UK; Faculty of Health and Medical Sciences, University of Western Australia; University of Leicester; Kjell och Märta Beijers Stiftelse; University of Miami; Eunice Kennedy Shriver National Institute of Child Health and Human Development; GlaxoSmithKline; Universidade Federal de Pelotas; KU Leuven; Duke-NUS Medical School; QIMR Berghofer Medical Research Institute; School of Public Health, University of Michigan; National Institute of Environmental Health Sciences; School of Medicine, Boston University; Steno Diabetes Center Copenhagen; McMaster University; Imperial College London; Det Sundhedsvidenskabelige Fakultet, Københavns Universitet; University of North Carolina at Chapel Hill; Science for Life Laboratory; National Science Foundation; Oak Foundation; Novo Nordisk Fonden; American Heart Association; University of California, Los Angeles; University of Washington; Brigham and Women's Hospital; Heart and Stroke Foundation of Canada; National Health and Medical Research Council; Oulun Yliopisto; NIHR Leicester Biomedical Research Centre; U.S. Department of Veterans Affairs","keywords":"Biology; Genome-wide association study; Association (psychology); Disease; Genetics; Sedentary behavior; Genetic association; Computational biology; Physical activity; Genome; Evolutionary biology; Gene; Single-nucleotide polymorphism; Genotype; Obesity; Psychology","score_opus":0.04293197152893032,"score_gpt":0.3769140334785058,"score_spread":0.3339820619495755,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4294904260","genre_codex":"review","genre_gemma":"review","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"review","genre_consensus":"review","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.00005155758,0.9990231,0.00012607292,0.0003628387,0.00014536126,0.0000026132357,0.000025788075,0.0000055292403,0.00025712108],"genre_scores_gemma":[0.0005048879,0.998781,0.000155899,0.0001997772,0.00013796655,0.000005613325,0.0000350595,0.0000017771009,0.00017795585],"study_design_codex":"design_other","study_design_gemma":"observational","domain_scores_codex":[0.9994779,0.00015944657,0.000071181785,0.000118667034,0.00013365742,0.00003918403],"domain_scores_gemma":[0.99754626,0.0016988544,0.00019812914,0.00005420027,0.00039026764,0.00011229839],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0021640419,0.0012979036,0.003091815,0.003006063,0.00019985448,0.0011333196,0.001200715,0.001644275,0.0038207397],"category_scores_gemma":[0.0029435612,0.00040772898,0.0011934737,0.0029464904,0.00067960384,0.00090939517,0.0007327837,0.0023789813,0.0017535366],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00021639906,0.00006380677,0.0008411574,0.022406481,0.000940139,0.00015138485,0.000030553634,0.00042179538,0.0005183046,0.0033923432,0.02419174,0.94682586],"study_design_scores_gemma":[0.00015304267,0.0002797285,0.009230884,0.02224557,0.00221489,0.0017426817,0.0001011504,0.00034941532,0.00056644244,0.008269693,0.9547676,0.00007887382],"about_ca_topic_score_codex":0.0018410049,"about_ca_topic_score_gemma":0.0029642293,"teacher_disagreement_score":0.0038207397,"about_ca_system_score_codex":0.0009193062,"about_ca_system_score_gemma":0.0015594845,"threshold_uncertainty_score":0.01278168},"labels":[],"label_agreement":null},{"id":"W4294904531","doi":"10.1038/s41588-022-01168-y","title":"Genetic determinants of chromatin reveal prostate cancer risk mediated by context-dependent gene regulation","year":2022,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Epigenetics and DNA Methylation","field":"Biochemistry, Genetics and Molecular Biology","cited_by":56,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of British Columbia","funders":"National Cancer Institute; National Human Genome Research Institute; National Institute of Mental Health; Pharmaceutical Research and Manufacturers of America Foundation","keywords":"Biology; Chromatin; Context (archaeology); Prostate cancer; Genetics; Gene; Cancer; Computational biology; Evolutionary biology","score_opus":0.005024607780222015,"score_gpt":0.25492823906071804,"score_spread":0.24990363128049603,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4294904531","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99361694,0.00078273984,0.0038283784,0.000089620036,0.000016163984,0.0000070984006,0.00026004808,0.00007423034,0.0013247357],"genre_scores_gemma":[0.999173,0.00007820326,0.0003896271,0.000016706152,0.0000051765533,0.000001856809,0.000047911628,0.000010934147,0.00027666744],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.99979407,0.00004189032,0.000008704134,0.00006511009,0.000051734893,0.00003856045],"domain_scores_gemma":[0.999683,0.00009382109,0.00008693044,0.000043369757,0.000024493747,0.0000683213],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00020939158,0.00017392317,0.0002100092,0.00043264963,0.00014686631,0.00034585394,0.00023064061,0.00017537747,0.002444047],"category_scores_gemma":[0.000413455,0.00022308301,0.0001761425,0.00023025983,0.0002852513,0.00014790912,0.00032832404,0.0004232857,0.00020299721],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00029560208,0.000021460506,0.01990324,0.000019646652,0.000036070614,0.00014759322,0.000055781762,0.00036881468,0.9743732,0.0011812997,0.000059145,0.003538113],"study_design_scores_gemma":[0.00001964446,0.0003300415,0.4851329,0.000012812735,0.00012168436,0.0018426548,0.00015404454,0.006616211,0.5013998,0.0023863707,0.0019423189,0.0000415495],"about_ca_topic_score_codex":0.0007388639,"about_ca_topic_score_gemma":0.001584357,"teacher_disagreement_score":0.002444047,"about_ca_system_score_codex":0.00018026574,"about_ca_system_score_gemma":0.00012954965,"threshold_uncertainty_score":0.008176208},"labels":[],"label_agreement":null},{"id":"W4297242151","doi":"10.1038/s41588-022-01171-3","title":"Identification of shared and differentiating genetic architecture for autism spectrum disorder, attention-deficit hyperactivity disorder and case subgroups","year":2022,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Autism Spectrum Disorder Research","field":"Neuroscience","cited_by":76,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Dalhousie University","funders":"National Institute of Arthritis and Musculoskeletal and Skin Diseases; National Institute of Mental Health; National Institute on Aging; Agència de Gestió d'Ajuts Universitaris i de Recerca; National Institutes of Health; H. Lundbeck A/S; Horizon 2020 Framework Programme; Novo Nordisk Fonden; Lundbeckfonden; Ministerio de Economía y Competitividad; Novo Nordisk; Generalitat de Catalunya; Aarhus Universitet; European Commission; Wellcome Trust; European College of Neuropsychopharmacology; Ministerio de Ciencia, Innovación y Universidades; National Alliance for Research on Schizophrenia and Depression","keywords":"Autism spectrum disorder; Biology; Attention deficit hyperactivity disorder; Genetic architecture; Identification (biology); Genetics; Autism; Neurodevelopmental disorder; Developmental psychology; Clinical psychology; Psychology; Gene; Phenotype; Ecology","score_opus":0.013662958355551853,"score_gpt":0.2793343809857884,"score_spread":0.2656714226302365,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4297242151","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99745053,0.00018288883,0.0013113082,0.000045992652,0.00000579038,0.000018689561,0.00053572416,0.000025172854,0.00042376158],"genre_scores_gemma":[0.9975018,0.000063333384,0.0010929224,0.000028665127,0.0000054104303,0.000025191606,0.0011388191,0.000027868164,0.00011603643],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9973909,0.000506314,0.00025807266,0.0013250556,0.00026891104,0.00025062016],"domain_scores_gemma":[0.99739575,0.0008531807,0.00076928496,0.0005476915,0.00018141582,0.000252615],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0016922179,0.00054336037,0.0006604733,0.0032070333,0.00075713673,0.0010534689,0.00058057706,0.0006230682,0.0021250611],"category_scores_gemma":[0.0043741018,0.00026372014,0.0010870787,0.0015311919,0.0006958542,0.00034588887,0.0016663847,0.00057602377,0.0002329894],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00041263812,0.000058757396,0.95031226,0.000040583203,0.0008434918,0.0012492111,0.0006392042,0.0003046142,0.0379508,0.00043610795,0.00030513084,0.0074472255],"study_design_scores_gemma":[0.000019864057,0.000053413674,0.9927429,0.000019381529,0.00039936363,0.0021396647,0.00032844083,0.0013909288,0.0018987363,0.0006174061,0.00037673852,0.000013249058],"about_ca_topic_score_codex":0.0042129466,"about_ca_topic_score_gemma":0.0069947117,"teacher_disagreement_score":0.0042129466,"about_ca_system_score_codex":0.00043484147,"about_ca_system_score_gemma":0.0005321821,"threshold_uncertainty_score":0.008949399},"labels":[],"label_agreement":null},{"id":"W4306412179","doi":"10.1038/s41588-022-01190-0","title":"Targeted profiling of human extrachromosomal DNA by CRISPR-CATCH","year":2022,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Cancer Genomics and Diagnostics","field":"Biochemistry, Genetics and Molecular Biology","cited_by":123,"is_retracted":false,"has_abstract":true,"route_ca_aff":false,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"","funders":"Deutsche Forschungsgemeinschaft; Rosetrees Trust; European Commission; National Human Genome Research Institute; Wellcome Trust; Francis Crick Institute; National Institutes of Health; Cancer Research UK; Jonsson Comprehensive Cancer Center; Canadian Institutes of Health Research; National Institute of General Medical Sciences; National Institute for Health and Care Research; National Cancer Institute; Melanoma Research Alliance; National Institute of Allergy and Infectious Diseases; Howard Hughes Medical Institute","keywords":"Biology; CRISPR; Extrachromosomal DNA; Genetics; DNA; Amplicon; Gene; Enhancer; Cas9; Computational biology; Gene expression; Plasmid; Polymerase chain reaction","score_opus":0.005729933780264319,"score_gpt":0.25760819296845966,"score_spread":0.25187825918819534,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4306412179","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.8631402,0.0016287718,0.12857166,0.00018069336,0.000046967958,0.0001212306,0.0022850865,0.0011310689,0.002894291],"genre_scores_gemma":[0.9242054,0.00111206,0.06662246,0.00015842041,0.000008930405,0.00011503938,0.0025906682,0.0002544105,0.004932631],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99973065,0.000022723247,0.000013710348,0.00011039055,0.000091210284,0.00003134358],"domain_scores_gemma":[0.9997141,0.00009516257,0.0000706632,0.00003997923,0.00004483559,0.000035290872],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00021090798,0.00029192728,0.00024571174,0.00031289313,0.00013101418,0.00035918647,0.00022360134,0.00043643796,0.0009277725],"category_scores_gemma":[0.00042369994,0.00019667747,0.00021461683,0.00017950778,0.00021656182,0.00017682875,0.0003755687,0.0004914342,0.00052034046],"study_design_candidate":"bench_or_experimental","study_design_consensus":"bench_or_experimental","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0000115280245,0.0000031629288,0.00017642757,0.000022965605,0.000004818358,0.000012849971,0.000010317319,0.000091437716,0.9984515,0.000035422534,0.000015913607,0.0011636894],"study_design_scores_gemma":[0.0000016575179,0.000044086704,0.0018730455,0.000003009276,0.0000070177666,0.00009971562,0.0000105232375,0.0008177682,0.9957243,0.00003657587,0.001378443,0.000003847224],"about_ca_topic_score_codex":0.0005877116,"about_ca_topic_score_gemma":0.0015617715,"teacher_disagreement_score":0.0009277725,"about_ca_system_score_codex":0.00026174923,"about_ca_system_score_gemma":0.00016191667,"threshold_uncertainty_score":0.003103733},"labels":[],"label_agreement":null},{"id":"W4306888850","doi":"10.1038/s41588-022-01192-y","title":"Discovery of 42 genome-wide significant loci associated with dyslexia","year":2022,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Reading and Literacy Development","field":"Psychology","cited_by":140,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Université du Québec à Chicoutimi; Université de Montréal; Centre Hospitalier Universitaire Sainte-Justine; Hospital for Sick Children; University of Toronto; University Health Network","funders":"National Center for Advancing Translational Sciences; National Natural Science Foundation of China; Max-Planck-Gesellschaft; Eunice Kennedy Shriver National Institute of Child Health and Human Development; Agence Nationale de la Recherche; Royal Society","keywords":"Dyslexia; Biology; Genome-wide association study; Heritability; Genetics; Reading disability; Reading (process); Developmental psychology; Psychology; Gene; Single-nucleotide polymorphism; Genotype","score_opus":0.009933108808174294,"score_gpt":0.26201750791710077,"score_spread":0.2520843991089265,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4306888850","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.998767,0.0002105371,0.00022466038,0.00006833242,0.000006321678,0.000006833792,0.0003257027,0.000013131064,0.00037757357],"genre_scores_gemma":[0.9985727,0.00013000387,0.00036143314,0.000045299254,0.0000098506325,0.0000072710664,0.0004832937,0.0000044361045,0.00038569933],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9996959,0.000045830206,0.000024887098,0.00012986592,0.000046888184,0.000056676305],"domain_scores_gemma":[0.99949026,0.00017846526,0.00012986585,0.000059591617,0.00004195678,0.00009985573],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00041183102,0.00030053352,0.00030397737,0.00078998646,0.00041542645,0.0005926495,0.00027208796,0.0003733729,0.0017180486],"category_scores_gemma":[0.0011136412,0.00018500212,0.00040570894,0.0006882456,0.00029972405,0.000097677956,0.00041291717,0.0003746636,0.00018567081],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0005840595,0.00007507917,0.945689,0.000052280513,0.00049129396,0.0019090399,0.0005230004,0.00021202545,0.038214803,0.00021438382,0.00039610473,0.011638852],"study_design_scores_gemma":[0.000022723481,0.00004549694,0.9978606,0.0000057116877,0.000101192665,0.0004683698,0.00005628687,0.0001302682,0.0008641517,0.00006793002,0.0003726729,0.0000046182463],"about_ca_topic_score_codex":0.0074553415,"about_ca_topic_score_gemma":0.009544319,"teacher_disagreement_score":0.0074553415,"about_ca_system_score_codex":0.00018117021,"about_ca_system_score_gemma":0.00032374344,"threshold_uncertainty_score":0.014823914},"labels":[],"label_agreement":null},{"id":"W4307494075","doi":"10.1038/s41588-022-01219-4","title":"Rare and common autism risk variants converge across 16p","year":2022,"lang":"en","type":"letter","venue":"Nature Genetics","topic":"Genomic variations and chromosomal abnormalities","field":"Biochemistry, Genetics and Molecular Biology","cited_by":1,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Université de Montréal; Centre Hospitalier Universitaire Sainte-Justine","funders":"National Institute of Mental Health; U.S. Department of Health and Human Services","keywords":"Biology; Autism; Genetics; Gene; Developmental psychology; Psychology","score_opus":0.005438526194925329,"score_gpt":0.23299708114067452,"score_spread":0.2275585549457492,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4307494075","genre_codex":"commentary","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":null,"domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.057210084,0.008600168,0.0038969473,0.86803603,0.031575117,0.00007929096,0.00046870296,0.00025015778,0.029883552],"genre_scores_gemma":[0.47018045,0.0072855856,0.005024674,0.37083727,0.12082183,0.00019620016,0.00029314603,0.00017438825,0.025186427],"study_design_codex":"not_applicable","study_design_gemma":"observational","domain_scores_codex":[0.9990103,0.0002109168,0.000108507105,0.00018367548,0.00032346204,0.000163077],"domain_scores_gemma":[0.99692106,0.002154437,0.00021684132,0.00015290879,0.00023679703,0.00031793522],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0010025587,0.0007733687,0.0009176277,0.0007938119,0.0012563224,0.0012382299,0.0007083646,0.011554169,0.0038813043],"category_scores_gemma":[0.0063980287,0.00040391085,0.00057516625,0.00065451284,0.0017272942,0.00096178363,0.000904193,0.0067554507,0.0012932152],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.002272645,0.00013691327,0.04008499,0.00025278598,0.00029260467,0.33631197,0.0010330988,0.0011188809,0.01877578,0.027702073,0.466567,0.10545128],"study_design_scores_gemma":[0.0012463261,0.00052365434,0.05219837,0.00040849173,0.0003760253,0.34880772,0.0016170659,0.005425669,0.0101034455,0.09868087,0.48038843,0.00022404022],"about_ca_topic_score_codex":0.0014143209,"about_ca_topic_score_gemma":0.0021737868,"teacher_disagreement_score":0.011554169,"about_ca_system_score_codex":0.00091166643,"about_ca_system_score_gemma":0.0004888372,"threshold_uncertainty_score":0.012984276},"labels":[],"label_agreement":null},{"id":"W4307657653","doi":"10.1038/s41588-022-01203-y","title":"Statistical and functional convergence of common and rare genetic influences on autism at chromosome 16p","year":2022,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Genomic variations and chromosomal abnormalities","field":"Biochemistry, Genetics and Molecular Biology","cited_by":55,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Toronto; SickKids Foundation; Hospital for Sick Children","funders":"National Human Genome Research Institute; Novo Nordisk Fonden; National Institute of Mental Health; Eunice Kennedy Shriver National Institute of Child Health and Human Development; Aarhus Universitet; National Institute of Neurological Disorders and Stroke; National Institute of General Medical Sciences; Novo Nordisk; National Cancer Institute; U.S. Department of Health and Human Services; National Institutes of Health; U.S. National Library of Medicine; H. Lundbeck A/S; Lundbeckfonden; Simons Foundation Autism Research Initiative","keywords":"Biology; Autism; Genetics; Chromosome; Evolutionary biology; Convergence (economics); Computational biology; Gene; Developmental psychology","score_opus":0.005960049162336067,"score_gpt":0.22249000807453817,"score_spread":0.21652995891220211,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4307657653","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.95851076,0.00024016289,0.039961442,0.0000734236,0.0000064688634,0.000013953343,0.0001527184,0.00012242689,0.0009186581],"genre_scores_gemma":[0.9959628,0.00004894127,0.0037477422,0.0000122529145,0.000008369591,0.000009646882,0.00010307883,0.00001971894,0.000087451],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9974687,0.0009911106,0.00014726692,0.0007225866,0.0005309125,0.0001394371],"domain_scores_gemma":[0.984781,0.0117830355,0.0013229393,0.0013686515,0.00037549433,0.00036885374],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0038819443,0.00038383622,0.0005007397,0.0024059778,0.00034102346,0.00080170843,0.00043305976,0.00029892757,0.0012444782],"category_scores_gemma":[0.012601016,0.00028439943,0.00066905195,0.0011483966,0.001586536,0.00054486125,0.0011416994,0.00060736376,0.00012045193],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0012948058,0.000071447066,0.6451764,0.00025711025,0.0015522459,0.0020892702,0.0007921509,0.021380698,0.2349457,0.008937781,0.00017490223,0.08332752],"study_design_scores_gemma":[0.00004148705,0.00024067317,0.9096119,0.000018857345,0.00039235965,0.0018768322,0.00031965852,0.054949313,0.017048225,0.014908265,0.0005301508,0.00006226602],"about_ca_topic_score_codex":0.0009896269,"about_ca_topic_score_gemma":0.0012252955,"teacher_disagreement_score":0.0038819443,"about_ca_system_score_codex":0.00028209243,"about_ca_system_score_gemma":0.00035299006,"threshold_uncertainty_score":0.020529926},"labels":[],"label_agreement":null},{"id":"W4308211464","doi":"10.1038/s41588-022-01213-w","title":"Multi-ancestry genome-wide association analyses identify novel genetic mechanisms in rheumatoid arthritis","year":2022,"lang":"en","type":"review","venue":"Nature Genetics","topic":"Lymphoma Diagnosis and Treatment","field":"Medicine","cited_by":348,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Toronto; Lunenfeld-Tanenbaum Research Institute","funders":"National Cancer Institute; National Human Genome Research Institute; Moonshot Research and Development Program; National Institute of Arthritis and Musculoskeletal and Skin Diseases; NIHR Maudsley Biomedical Research Centre; National Institutes of Health; Kementerian Kesihatan Malaysia; Versus Arthritis; Kanae Foundation for the Promotion of Medical Science; Instituto de Salud Carlos III; Astellas Foundation for Research on Metabolic Disorders; Astellas Pharma; Vetenskapsrådet; Foundation for the National Institutes of Health; Fonds National de la Recherche Luxembourg; Wellcome Trust; European League Against Rheumatism; King's College London; Tokyo Medical and Dental University; National Institute for Health and Care Research; Ministerio de Ciencia e Innovación; Japan Agency for Medical Research and Development; Qatar National Research Fund; Qatar Foundation; National Center for Advancing Translational Sciences; Department of Health and Social Care; Japan Society for the Promotion of Science; Mochida Memorial Foundation for Medical and Pharmaceutical Research","keywords":"Genome-wide association study; Biology; Genetic genealogy; Genetic association; Genetics; Genetic architecture; Rheumatoid arthritis; 1000 Genomes Project; Evolutionary biology; Computational biology; Single-nucleotide polymorphism; Gene; Genotype; Quantitative trait locus; Population; Medicine; Immunology","score_opus":0.06789304924686873,"score_gpt":0.37702505468534914,"score_spread":0.3091320054384804,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4308211464","genre_codex":"review","genre_gemma":"review","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"review","genre_consensus":"review","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.0000655174,0.9990575,0.00010740626,0.00033551193,0.00013054468,0.0000016952383,0.000020202337,0.000005698733,0.00027603118],"genre_scores_gemma":[0.0006345296,0.99821067,0.00019102257,0.00037749822,0.0002957078,0.0000036651068,0.00004393645,0.0000014154023,0.00024152307],"study_design_codex":"design_other","study_design_gemma":"observational","domain_scores_codex":[0.9997187,0.000057889847,0.000046139245,0.000067595836,0.000084200154,0.000025358113],"domain_scores_gemma":[0.9991166,0.0005791634,0.00010554876,0.000019623305,0.00012605636,0.000053119937],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0010351025,0.0010589286,0.0022286728,0.0016667141,0.00019282871,0.0010144662,0.0012524191,0.0013918113,0.0027654779],"category_scores_gemma":[0.0014097844,0.00031741677,0.00076416024,0.0019775059,0.0004886744,0.00082742685,0.00078262616,0.002090609,0.001320884],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00016515507,0.000037439215,0.0005390967,0.0098708365,0.00039881727,0.00022110858,0.000022303548,0.00028717733,0.00081917486,0.0020794289,0.02463787,0.9609216],"study_design_scores_gemma":[0.00017561318,0.00015909814,0.007111582,0.010451654,0.0017687168,0.0024119199,0.00009462867,0.00024582478,0.00049665954,0.007326053,0.9696832,0.000074988195],"about_ca_topic_score_codex":0.0015002433,"about_ca_topic_score_gemma":0.0033183943,"teacher_disagreement_score":0.0027654779,"about_ca_system_score_codex":0.00057053776,"about_ca_system_score_gemma":0.0010125606,"threshold_uncertainty_score":0.009251416},"labels":[],"label_agreement":null},{"id":"W4309664456","doi":"10.1038/s41588-022-01208-7","title":"Exome sequencing identifies rare damaging variants in ATP8B4 and ABCA1 as risk factors for Alzheimer’s disease","year":2022,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Alzheimer's disease research and treatments","field":"Medicine","cited_by":219,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"McGill University and Génome Québec Innovation Centre","funders":"National Heart, Lung, and Blood Institute; National Institute on Aging; University of California, San Francisco; Nederlandse Organisatie voor Wetenschappelijk Onderzoek; New York Genome Center; Agence Nationale de la Recherche; Alzheimer's Disease Neuroimaging Initiative; National Institute of Neurological Disorders and Stroke; Medical Research Council; Alzheimer's Association","keywords":"TREM2; Biology; Exome sequencing; Genome-wide association study; Genetics; Loss function; Genetic association; Disease; Exome; Dementia; Alzheimer's disease; Gene; Bioinformatics; Single-nucleotide polymorphism; Mutation; Genotype; Medicine; Phenotype; Internal medicine","score_opus":0.033394346761479135,"score_gpt":0.3322903925668842,"score_spread":0.2988960458054051,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4309664456","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9942334,0.0020103045,0.001448584,0.0002479637,0.000040352268,0.000007995629,0.0014698425,0.000027019603,0.0005145198],"genre_scores_gemma":[0.99723685,0.000482617,0.00075091136,0.00013126206,0.000035470555,0.000007844457,0.0009937803,0.000009960746,0.00035128565],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99963164,0.00008132388,0.000041675685,0.0001340225,0.00006862763,0.000042704785],"domain_scores_gemma":[0.99913126,0.000373739,0.0002572551,0.00007804085,0.000080499856,0.00007915137],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.000548765,0.00044656135,0.0004472393,0.0008942624,0.00032910623,0.0006153182,0.00028479096,0.00077021646,0.0036592588],"category_scores_gemma":[0.0020006066,0.00014698693,0.00033599656,0.00089944253,0.00021908498,0.00025765193,0.00044094303,0.0004526206,0.00034630924],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0027752782,0.00012446086,0.8300819,0.00026204897,0.001308556,0.0062990496,0.00042450256,0.0007975304,0.12027016,0.0006449851,0.0028812196,0.034130435],"study_design_scores_gemma":[0.00008377801,0.00017468249,0.97867537,0.000073390314,0.0005099265,0.007524889,0.00018793062,0.0021227829,0.0061487914,0.0012168031,0.00325927,0.000022381842],"about_ca_topic_score_codex":0.0009878625,"about_ca_topic_score_gemma":0.0011361046,"teacher_disagreement_score":0.0036592588,"about_ca_system_score_codex":0.00012392981,"about_ca_system_score_gemma":0.00008882035,"threshold_uncertainty_score":0.012241423},"labels":[],"label_agreement":null},{"id":"W4310493943","doi":"10.1038/s41588-022-01230-9","title":"The genomic and immune landscape of long-term survivors of high-grade serous ovarian cancer","year":2022,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Ovarian cancer diagnosis and treatment","field":"Medicine","cited_by":113,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Victoria; University of British Columbia","funders":"Cancer Council Tasmania; Cancer Council South Australia; Medical Research Council; Medical Research and Materiel Command; Genentech; Uniscientia Foundation; BC Cancer Foundation; Swiss Cancer Research Foundation; Cancer Council Victoria; Eisai; Cancer Australia; Cancer Council NSW; National Health and Medical Research Council; Cancer Research UK; Clovis Oncology; Peter MacCallum Cancer Centre; BeiGene; Genome British Columbia; Cancer Institute NSW; National Cancer Institute; Ovarian Cancer Australia; AstraZeneca; Eli Lilly and Company","keywords":"Biology; Ovarian cancer; Somatic cell; Transcriptome; Serous fluid; Immune system; Germline; DNA methylation; Phenotype; Survival analysis; Cancer; Gene; Genetics; Bioinformatics; Oncology; Internal medicine; Gene expression; Medicine","score_opus":0.008226354714891852,"score_gpt":0.25872593173459696,"score_spread":0.2504995770197051,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4310493943","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99770564,0.000998605,0.0000961512,0.0002452274,0.000007993012,0.0000026883613,0.00023772131,0.000004463915,0.0007016331],"genre_scores_gemma":[0.9988192,0.00038690522,0.000039799746,0.00010792878,0.000020011692,0.0000034075317,0.00022610604,0.0000038842786,0.00039280136],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99987507,0.000027620426,0.000005558816,0.000026785036,0.000019307392,0.000045588047],"domain_scores_gemma":[0.99968994,0.00008154578,0.00010907131,0.000020126561,0.00003206828,0.000067344816],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00012220896,0.00008050739,0.00016281137,0.00032606503,0.000263824,0.00047932006,0.00016555772,0.00028849777,0.0018207566],"category_scores_gemma":[0.0008319221,0.00008487568,0.00010914558,0.00044382835,0.00021654509,0.00026196943,0.00029798743,0.0003187991,0.00015737233],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00051424996,0.000072150244,0.951238,0.00004358757,0.00009947026,0.0007037891,0.00045569672,0.00031888144,0.024142336,0.0005687112,0.0008321539,0.021011064],"study_design_scores_gemma":[0.000005395465,0.00013903122,0.995839,0.000008880699,0.000040969513,0.0009071064,0.000548924,0.00017665482,0.000595226,0.00049156684,0.001241968,0.000005267871],"about_ca_topic_score_codex":0.0011752594,"about_ca_topic_score_gemma":0.0017837103,"teacher_disagreement_score":0.0018207566,"about_ca_system_score_codex":0.0001639039,"about_ca_system_score_gemma":0.00017790943,"threshold_uncertainty_score":0.0060909986},"labels":[],"label_agreement":null},{"id":"W4311086202","doi":"10.1038/s41588-022-01205-w","title":"K27M in canonical and noncanonical H3 variants occurs in distinct oligodendroglial cell lineages in brain midline gliomas","year":2022,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Glioma Diagnosis and Treatment","field":"Medicine","cited_by":158,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"McGill Genome Centre; Montreal Children's Hospital; Université Laval; Université de Montréal; Centre Hospitalier Universitaire Sainte-Justine; Hospital for Sick Children; McGill University Health Centre; McGill University; SickKids Foundation; University of Toronto; Jewish General Hospital","funders":"Eunice Kennedy Shriver National Institute of Child Health and Human Development; National Cancer Institute; Brain Research UK","keywords":"Biology; Chromatin; Histone H3; Epigenomics; Genetics; Epigenetics; Transcriptome; Mutation; Histone; Cell biology; DNA methylation; Gene; Gene expression","score_opus":0.008924336558614337,"score_gpt":0.280216542590572,"score_spread":0.27129220603195764,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4311086202","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9975278,0.0004205032,0.0006577009,0.00007418696,0.000011637885,0.000006910413,0.00021148253,0.00003250621,0.0010572185],"genre_scores_gemma":[0.9989108,0.00008932359,0.00021623001,0.00004538206,0.0000047379563,0.000003817252,0.00017062337,0.00003345478,0.00052561966],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.99969566,0.000024753306,0.00002645733,0.00007387612,0.00008765037,0.00009171481],"domain_scores_gemma":[0.99970007,0.00004279798,0.00010878144,0.0000347758,0.00004020153,0.00007343826],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00016489098,0.00019738798,0.00020509606,0.00058101164,0.00029919358,0.00038200812,0.00037774484,0.0003820538,0.0032993848],"category_scores_gemma":[0.000461203,0.00019530265,0.00028784474,0.00033612375,0.0004953369,0.00021546999,0.0005310658,0.00037571214,0.0007119801],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0019432317,0.00005323779,0.098187126,0.00007811311,0.00020560388,0.0035905363,0.00026422026,0.00045939427,0.88192993,0.0012545255,0.0008585529,0.011175559],"study_design_scores_gemma":[0.00015527985,0.0005080318,0.7084419,0.000057836278,0.00023308554,0.02979782,0.0012816527,0.003659872,0.24231638,0.003234368,0.01024486,0.00006885102],"about_ca_topic_score_codex":0.0030218412,"about_ca_topic_score_gemma":0.0062374542,"teacher_disagreement_score":0.0032993848,"about_ca_system_score_codex":0.00043438817,"about_ca_system_score_gemma":0.00028819125,"threshold_uncertainty_score":0.0110375285},"labels":[],"label_agreement":null},{"id":"W4311671146","doi":"10.1038/s41588-022-01240-7","title":"Antagonistic control of seed dormancy in rice by two bHLH transcription factors","year":2022,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Seed Germination and Physiology","field":"Agricultural and Biological Sciences","cited_by":145,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Institute of Genetics","funders":"Ministry of Science and Technology of the People's Republic of China; Chinese Academy of Sciences; National Natural Science Foundation of China","keywords":"Biology; Seed dormancy; Dormancy; Transcription factor; Gene; Enhancer; Genetics; Quantitative trait locus; Locus (genetics); Germination; Botany","score_opus":0.009071428057731798,"score_gpt":0.23418112582143377,"score_spread":0.225109697763702,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4311671146","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9952165,0.0005458661,0.0021307163,0.000113019116,0.000022196855,0.000006946063,0.00007946627,0.000046578567,0.0018387937],"genre_scores_gemma":[0.99653745,0.000096896496,0.0009032264,0.00010378844,0.000009621449,0.0000107071755,0.00013709132,0.000035113237,0.0021661809],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9997745,0.000039790506,0.000014801565,0.000052019786,0.00004315056,0.00007572516],"domain_scores_gemma":[0.99963284,0.00008867875,0.00006429325,0.0000416014,0.000032123135,0.0001403667],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0002832961,0.00036745204,0.00030510683,0.00036881055,0.0002537143,0.000416052,0.00040561575,0.00027202646,0.0011416145],"category_scores_gemma":[0.00024660735,0.00031238224,0.000268648,0.00012803309,0.00047605622,0.00027548417,0.00071460905,0.00076377176,0.00032936363],"study_design_candidate":"bench_or_experimental","study_design_consensus":"bench_or_experimental","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00014054481,0.000006241841,0.00019243587,0.000006297033,0.0000014521222,0.000024608615,0.000015582438,0.000011376201,0.99910444,0.00013564769,0.000010205489,0.00035123085],"study_design_scores_gemma":[0.00015234195,0.0004245019,0.06960495,0.000009202116,0.00004288094,0.0007673223,0.00028445755,0.0033053653,0.92241776,0.00067925383,0.0022811708,0.00003094117],"about_ca_topic_score_codex":0.0008987328,"about_ca_topic_score_gemma":0.0015092209,"teacher_disagreement_score":0.0011416145,"about_ca_system_score_codex":0.00058110827,"about_ca_system_score_gemma":0.00024880562,"threshold_uncertainty_score":0.0042163134},"labels":[],"label_agreement":null},{"id":"W4312066528","doi":"10.1038/s41588-022-01222-9","title":"Deciphering colorectal cancer genetics through multi-omic analysis of 100,204 cases and 154,587 controls of European and east Asian ancestries","year":2022,"lang":"en","type":"review","venue":"Nature Genetics","topic":"Genetic factors in colorectal cancer","field":"Medicine","cited_by":242,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Memorial University of Newfoundland; Lunenfeld-Tanenbaum Research Institute; Ontario Institute for Cancer Research; University of Toronto; Mount Sinai Hospital","funders":"Institute of Genetics; National Institute of Environmental Health Sciences; National Heart, Lung, and Blood Institute; Medical Research Council; School of Medicine, Vanderbilt University; Universitat de Barcelona; Vanderbilt-Ingram Cancer Center; University of Oxford; USC Norris Comprehensive Cancer Center; University of Southern California; World Health Organization; Cancer Research UK; Vanderbilt University Medical Center; European Commission; Case Comprehensive Cancer Center, Case Western Reserve University; University of Washington; National Cancer Institute; Cleveland Clinic; Vanderbilt University; Fred Hutchinson Cancer Research Center; Cancer Research Wales; National Institutes of Health; Office of Research Infrastructure Programs, National Institutes of Health; Syddansk Universitet; U.S. Department of Health and Human Services","keywords":"Biology; Colorectal cancer; Computational biology; Cancer; Genetics","score_opus":0.06861861033490717,"score_gpt":0.3693274227146368,"score_spread":0.30070881237972963,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4312066528","genre_codex":"review","genre_gemma":"review","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"review","genre_consensus":"review","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.0016745875,0.9970957,0.00026568733,0.00022602327,0.00009457883,0.000006853306,0.00017644292,0.000008275231,0.00045185714],"genre_scores_gemma":[0.0076309275,0.9898072,0.0010919806,0.00036221868,0.00012027268,0.0000095140285,0.0006278508,0.0000047024705,0.00034523485],"study_design_codex":"design_other","study_design_gemma":"observational","domain_scores_codex":[0.9996568,0.000072232695,0.00007486925,0.00007132147,0.000097732314,0.000027094751],"domain_scores_gemma":[0.9991689,0.00054729905,0.00011111274,0.000033749722,0.00010750535,0.000031446834],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0012647706,0.0006862931,0.0015621255,0.0019950753,0.00012019904,0.0006076472,0.000607123,0.0006022895,0.001296768],"category_scores_gemma":[0.0017512792,0.00024344097,0.0009257055,0.0021304747,0.0001910615,0.00047253046,0.00048365863,0.00052702887,0.0003731327],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0002813885,0.000039898907,0.009160594,0.030672891,0.003270796,0.0010157818,0.00013744312,0.00025930337,0.0050930623,0.0011211877,0.0126174465,0.93633026],"study_design_scores_gemma":[0.00025054842,0.00036274834,0.09497285,0.021594923,0.021698551,0.009501968,0.00034507015,0.00035446155,0.00394746,0.0038928317,0.8429461,0.00013238403],"about_ca_topic_score_codex":0.0019366947,"about_ca_topic_score_gemma":0.0040283375,"teacher_disagreement_score":0.0019950753,"about_ca_system_score_codex":0.0002925079,"about_ca_system_score_gemma":0.0009936355,"threshold_uncertainty_score":0.0066887736},"labels":[],"label_agreement":null},{"id":"W4312094292","doi":"10.1038/s41588-022-01261-2","title":"A genome-wide CRISPR screen identifies CALCOCO2 as a regulator of beta cell function influencing type 2 diabetes risk","year":2022,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Pancreatic function and diabetes","field":"Medicine","cited_by":58,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Alberta","funders":"National Center for Research Resources; Wellcome; Canadian Institutes of Health Research; University of Oxford; National Institute of Diabetes and Digestive and Kidney Diseases; Stanford Diabetes Research Center; National Institutes of Health; U.S. Department of Health and Human Services; Vertex Pharmaceuticals; Wellcome Trust; European Foundation for the Study of Diabetes; AstraZeneca","keywords":"Biology; CRISPR; Genome-wide association study; Genetics; Type 2 diabetes; Genetic screen; Proinsulin; Effector; Genome; Phenotype; Locus (genetics); Gene; Cell type; Computational biology; Cell biology; Insulin; Cell; Single-nucleotide polymorphism; Diabetes mellitus; Genotype; Endocrinology","score_opus":0.007107235206224306,"score_gpt":0.23729990443406676,"score_spread":0.23019266922784246,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4312094292","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.986901,0.00053158007,0.0073651904,0.00023264797,0.00004340519,0.000048054466,0.0023588238,0.0003399864,0.0021792618],"genre_scores_gemma":[0.9932145,0.0002865939,0.0040776148,0.00016811646,0.000010990174,0.000025111814,0.000994693,0.000065233064,0.0011572049],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99980015,0.00002851985,0.000012662415,0.000068714195,0.00005954873,0.000030439063],"domain_scores_gemma":[0.9997142,0.000119828015,0.00006099775,0.000023815684,0.000014892619,0.00006626258],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00023161927,0.00044444305,0.00035354306,0.0005351242,0.00028616,0.00053429394,0.0003412983,0.0005154393,0.0026337474],"category_scores_gemma":[0.00033745528,0.00016335906,0.00035160081,0.00036365076,0.00029971378,0.00007384941,0.00042437477,0.0004565639,0.00030540774],"study_design_candidate":"bench_or_experimental","study_design_consensus":"bench_or_experimental","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00042806825,0.000050162762,0.005966112,0.000052018597,0.00007511352,0.0010188502,0.000040289884,0.00067416264,0.9862665,0.0003553938,0.00023017265,0.004843054],"study_design_scores_gemma":[0.00025491926,0.0009050649,0.1815097,0.000081881284,0.0007828714,0.006907222,0.00031177947,0.016412344,0.77690333,0.00090846594,0.014912069,0.00011046833],"about_ca_topic_score_codex":0.001674542,"about_ca_topic_score_gemma":0.003502285,"teacher_disagreement_score":0.0026337474,"about_ca_system_score_codex":0.00026008947,"about_ca_system_score_gemma":0.0003712352,"threshold_uncertainty_score":0.008810759},"labels":[],"label_agreement":null},{"id":"W4312181330","doi":"10.1038/s41588-022-01225-6","title":"Powerful, scalable and resource-efficient meta-analysis of rare variant associations in large whole genome sequencing studies","year":2022,"lang":"en","type":"review","venue":"Nature Genetics","topic":"Genetic Associations and Epidemiology","field":"Biochemistry, Genetics and Molecular Biology","cited_by":62,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Saskatchewan; Université de Montréal; Université Laval; University of Ottawa; McGill University; University of Calgary","funders":"National Institute on Minority Health and Health Disparities; National Center for Research Resources; National Institute of Environmental Health Sciences; National Human Genome Research Institute; National Institute of Nursing Research; National Institute of Mental Health; National Heart, Lung, and Blood Institute; National Institute on Aging; National Institute of Diabetes and Digestive and Kidney Diseases; National Institute of Arthritis and Musculoskeletal and Skin Diseases; National Center for Advancing Translational Sciences; Medical Research Council; National Institute of Neurological Disorders and Stroke; Evans Medical Foundation; School of Medicine, Boston University; American Heart Association; Broad Institute; Johns Hopkins University; Children's Hospital of Philadelphia; Wake Forest University; National Cancer Institute; American Diabetes Association; Emory University; University of Pennsylvania; National Institutes of Health; U.S. Department of Health and Human Services","keywords":"Biobank; Biology; Meta-analysis; Whole genome sequencing; Computational biology; Exome sequencing; Exome; Genome-wide association study; Genetics; Bioinformatics; Genome; Phenotype; Single-nucleotide polymorphism; Genotype; Gene; Medicine","score_opus":0.0712440556957609,"score_gpt":0.3565136436337957,"score_spread":0.2852695879380348,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4312181330","genre_codex":"review","genre_gemma":"review","domain_codex":null,"domain_gemma":"methods","model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"review","genre_consensus":"review","domain_candidate":"methods","domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.0011557165,0.93604314,0.0568371,0.0018638741,0.00068720867,0.00007517487,0.0019165103,0.00080362754,0.00061753864],"genre_scores_gemma":[0.021464406,0.8464373,0.11843559,0.0026680161,0.002242275,0.00034728285,0.006544191,0.0005427325,0.0013182352],"study_design_codex":"design_other","study_design_gemma":"meta_analysis","domain_scores_codex":[0.9960366,0.0019090917,0.00028235847,0.00074296515,0.00087170507,0.0001574283],"domain_scores_gemma":[0.98587626,0.011706095,0.00059729465,0.0007486154,0.0008172416,0.00025448285],"candidate_categories":["metaresearch"],"consensus_categories":[],"category_scores_codex":[0.01082604,0.0026584903,0.0063581695,0.0029322933,0.00024622417,0.0023998169,0.004002435,0.001379149,0.0030044785],"category_scores_gemma":[0.017851338,0.0012644732,0.004213581,0.0042638797,0.0005683473,0.0013634071,0.0018990292,0.0037327043,0.0016668863],"study_design_candidate":"meta_analysis","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00056459603,0.000074366326,0.003090863,0.0108352415,0.013377261,0.00018810798,0.00005242879,0.0057921335,0.0024762172,0.0037976375,0.025196698,0.9345544],"study_design_scores_gemma":[0.0025701975,0.0010620726,0.040405825,0.016047021,0.05007843,0.005979413,0.00020793667,0.04693803,0.008029926,0.16390197,0.66411525,0.000663878],"about_ca_topic_score_codex":0.0032724582,"about_ca_topic_score_gemma":0.006978901,"teacher_disagreement_score":0.98917395,"about_ca_system_score_codex":0.0006498407,"about_ca_system_score_gemma":0.002215794,"threshold_uncertainty_score":0.057254255},"labels":[],"label_agreement":null},{"id":"W4313830852","doi":"10.1038/s41588-022-01254-1","title":"Single-cell transcriptomic analysis of endometriosis","year":2023,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Endometriosis Research and Treatment","field":"Medicine","cited_by":183,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Vancouver General Hospital; University of British Columbia; University of British Columbia Hospital","funders":"Clinical and Translational Science Institute, University of California, Los Angeles; National Institute of Biomedical Imaging and Bioengineering; Michael Smith Health Research BC; Canadian Cancer Society Research Institute; U.S. Department of Health and Human Services; National Institutes of Health; National Center for Advancing Translational Sciences; BC Cancer Foundation; Cedars-Sinai Medical Center; Government of Canada; Ovarian Cancer Research Alliance; National Institute of Allergy and Infectious Diseases; Canadian Institutes of Health Research; American Cancer Society","keywords":"Stromal cell; Endometriosis; Biology; Epithelium; Stroma; Cancer research; Downregulation and upregulation; Cell type; Transcriptome; Endometrium; Somatic cell; Pathology; Cell; Endocrinology; Immunology; Medicine; Genetics; Immunohistochemistry; Gene expression; Gene","score_opus":0.027198757442484425,"score_gpt":0.31493136783375225,"score_spread":0.28773261039126785,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4313830852","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.95533365,0.0041202963,0.017794218,0.00047158587,0.00020414799,0.00006751638,0.017847192,0.00026021508,0.003901167],"genre_scores_gemma":[0.9639132,0.0027606578,0.014033302,0.0004505436,0.00006785663,0.00012582974,0.014848407,0.00011691211,0.0036831857],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9998704,0.000010031745,0.0000067130127,0.000047904894,0.000040294788,0.000024647172],"domain_scores_gemma":[0.99990404,0.000034645636,0.000013013617,0.000013108006,0.000019858615,0.000015273745],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00014320387,0.00013637533,0.00040278674,0.00035059496,0.00029487783,0.00057802594,0.00017805012,0.00036300873,0.0013248741],"category_scores_gemma":[0.00028089518,0.00013626977,0.00038084527,0.00042163557,0.00018148194,0.00020634102,0.00031350914,0.00046295804,0.0004899279],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.000084643245,0.00000825748,0.0021637355,0.00010020365,0.000028537812,0.00007501257,0.000044431443,0.00035155241,0.9925648,0.00019894398,0.00036716173,0.0040128124],"study_design_scores_gemma":[0.00005138014,0.0004136347,0.3375528,0.000080487,0.00022477607,0.0014790074,0.0009968287,0.023108473,0.60234696,0.0021685737,0.031498972,0.00007818101],"about_ca_topic_score_codex":0.00065564323,"about_ca_topic_score_gemma":0.0023408094,"teacher_disagreement_score":0.0013248741,"about_ca_system_score_codex":0.00020245677,"about_ca_system_score_gemma":0.00020914576,"threshold_uncertainty_score":0.004432082},"labels":[],"label_agreement":null},{"id":"W4315779240","doi":"10.1038/s41588-022-01270-1","title":"Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases","year":2023,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Genetic Associations and Epidemiology","field":"Biochemistry, Genetics and Molecular Biology","cited_by":972,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"McGill University Health Centre; McGill Genome Centre; Impact; McGill University; McMaster University; Jewish General Hospital","funders":"Fonds de Recherche du Québec - Santé; National Institutes of Health; European Commission; Jewish General Hospital; National Institute for Health and Care Research; Canadian Institutes of Health Research; Compute Canada; Novo Nordisk Fonden; Cancer Research UK; Public Health Agency; GlaxoSmithKline; Government of Canada; McGill University; Public Health Agency of Canada; Wellcome Trust; Medical Research Council; Biogen; AstraZeneca; Eli Lilly and Company","keywords":"Mendelian randomization; Metabolome; Metabolite; Biology; Metabolomics; Genome-wide association study; Genetics; Quantitative trait locus; Genetic association; Expression quantitative trait loci; Gene; Bioinformatics; Genotype; Endocrinology; Single-nucleotide polymorphism; Genetic variants","score_opus":0.009273071125204856,"score_gpt":0.2781213896259809,"score_spread":0.268848318500776,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4315779240","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.6170396,0.008317241,0.046663996,0.0023904499,0.00032570833,0.00017362396,0.30574775,0.0038628338,0.015478823],"genre_scores_gemma":[0.8268197,0.00419192,0.051597223,0.0009714005,0.00023583882,0.00025577145,0.11030518,0.0005031249,0.0051197414],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99973625,0.000049408183,0.000019325968,0.00010934695,0.000046905596,0.000038777674],"domain_scores_gemma":[0.9992781,0.0002431347,0.00019005944,0.00008282867,0.00010374628,0.000102141144],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00035343794,0.00060098874,0.000658975,0.003604793,0.00045108955,0.000979354,0.00034920615,0.00045976232,0.007334004],"category_scores_gemma":[0.0012295699,0.00019437062,0.00067260023,0.003736556,0.00017675525,0.00022925585,0.0008751316,0.0005306835,0.0010609389],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0040877606,0.00017438966,0.45787895,0.00201847,0.0031417767,0.0031347044,0.00039637132,0.006463362,0.2923691,0.008754582,0.044099648,0.17748082],"study_design_scores_gemma":[0.00019166646,0.0003015846,0.8618358,0.00018105978,0.0014303671,0.004584842,0.00026354293,0.00556643,0.027028792,0.013592665,0.0849096,0.00011369353],"about_ca_topic_score_codex":0.0028478683,"about_ca_topic_score_gemma":0.0073855007,"teacher_disagreement_score":0.007334004,"about_ca_system_score_codex":0.00031207208,"about_ca_system_score_gemma":0.00066844304,"threshold_uncertainty_score":0.024534643},"labels":[],"label_agreement":null},{"id":"W4318071643","doi":"10.1038/s41588-022-01285-8","title":"Genome-wide analyses of ADHD identify 27 risk loci, refine the genetic architecture and implicate several cognitive domains","year":2023,"lang":"en","type":"review","venue":"Nature Genetics","topic":"Attention Deficit Hyperactivity Disorder","field":"Medicine","cited_by":760,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Hospital for Sick Children; Douglas Mental Health University Institute; McGill University","funders":"National Institute of Mental Health; Instituto de Salud Carlos III; Agència de Gestió d'Ajuts Universitaris i de Recerca; Medical Research Council; National Institutes of Health; National Health and Medical Research Council; Horizon 2020 Framework Programme; Norges Forskningsråd; Novo Nordisk Fonden; Nederlandse Organisatie voor Wetenschappelijk Onderzoek; H. Lundbeck A/S; Lundbeckfonden; Novo Nordisk; Generalitat de Catalunya; European Regional Development Fund; Aarhus Universitet; European Commission; European College of Neuropsychopharmacology; Ministerio de Ciencia, Innovación y Universidades","keywords":"Biology; Genetic architecture; Genome-wide association study; Computational biology; Cognition; Genetics; Genome; Evolutionary biology; Quantitative trait locus; Neuroscience; Single-nucleotide polymorphism; Gene; Genotype","score_opus":0.0921700237096709,"score_gpt":0.4289418258005497,"score_spread":0.33677180209087876,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4318071643","genre_codex":"review","genre_gemma":"review","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"review","genre_consensus":"review","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.00021142975,0.9988894,0.00015396005,0.0002227067,0.000047607387,0.0000039548936,0.00007193741,0.000009024078,0.00039009826],"genre_scores_gemma":[0.0022436853,0.9968262,0.00036730734,0.00020823184,0.000043800002,0.0000067129904,0.00013773645,0.000002308101,0.00016411293],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.9997558,0.000053721375,0.00003887296,0.000060356346,0.00006819626,0.000023088229],"domain_scores_gemma":[0.99931204,0.00045155437,0.00008053531,0.000016027781,0.00010560394,0.000034262288],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0011953999,0.0010264091,0.0020633955,0.0030078741,0.00019340597,0.0008559619,0.00092034385,0.00079023413,0.0022852805],"category_scores_gemma":[0.0013891623,0.00022211226,0.0013422167,0.0030745864,0.00031794497,0.00055165676,0.00048727964,0.0010240971,0.000695299],"study_design_candidate":"not_applicable","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00021326347,0.000030548243,0.002090591,0.031610623,0.0019612708,0.00024783178,0.000047626778,0.00050379353,0.0010867572,0.0015782717,0.010948535,0.94968086],"study_design_scores_gemma":[0.00018081377,0.00029789156,0.024718676,0.028734047,0.013244172,0.0041668518,0.00020978366,0.00040638587,0.0013361094,0.004518396,0.92210734,0.00007957313],"about_ca_topic_score_codex":0.0030047342,"about_ca_topic_score_gemma":0.006778211,"teacher_disagreement_score":0.0030078741,"about_ca_system_score_codex":0.0007080852,"about_ca_system_score_gemma":0.001552759,"threshold_uncertainty_score":0.007645011},"labels":[],"label_agreement":null},{"id":"W4318486619","doi":"10.1038/s41588-022-01295-6","title":"Enhancer–promoter interactions can bypass CTCF-mediated boundaries and contribute to phenotypic robustness","year":2023,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Genomics and Chromatin Dynamics","field":"Biochemistry, Genetics and Molecular Biology","cited_by":113,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Toronto","funders":"Eunice Kennedy Shriver National Institute of Child Health and Human Development; U.S. Department of Health and Human Services; Government of Canada; National Institutes of Health; National Cancer Institute; Canadian Institutes of Health Research","keywords":"Biology; CTCF; Enhancer; Phenotype; Robustness (evolution); Genetics; Computational biology; Evolutionary biology; Gene; Transcription factor","score_opus":0.004471244183437778,"score_gpt":0.24257009181850123,"score_spread":0.23809884763506345,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4318486619","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9360071,0.00095255615,0.052367076,0.00047174626,0.00013640085,0.000041648655,0.00024365057,0.001316654,0.008463166],"genre_scores_gemma":[0.9945714,0.00009064963,0.0032327748,0.00014483393,0.000017321438,0.000025064382,0.00015344309,0.00026404997,0.0015003749],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.999373,0.00008090606,0.00004792867,0.00019833379,0.00018150921,0.00011826314],"domain_scores_gemma":[0.99883133,0.00038393209,0.00022158895,0.0002894674,0.000058635993,0.00021510058],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0004911637,0.00058577076,0.0006045621,0.00038011494,0.000429921,0.0012533291,0.0009128551,0.0012181196,0.004410262],"category_scores_gemma":[0.0015713277,0.00061346666,0.0004953959,0.00021265121,0.00084415724,0.0011939649,0.0022319134,0.0027421333,0.0014707581],"study_design_candidate":"bench_or_experimental","study_design_consensus":"bench_or_experimental","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00004773258,0.000019420493,0.0003263878,0.000016745376,0.000008354387,0.00011466197,0.000012948168,0.00037982222,0.99651426,0.0010470673,0.00004488699,0.0014677978],"study_design_scores_gemma":[0.00004542431,0.00009060622,0.0073995055,0.000009750018,0.000024903287,0.00069421186,0.00005333922,0.010315985,0.9748946,0.002936938,0.0035021706,0.00003264192],"about_ca_topic_score_codex":0.00022244967,"about_ca_topic_score_gemma":0.0004283254,"teacher_disagreement_score":0.004410262,"about_ca_system_score_codex":0.00042720567,"about_ca_system_score_gemma":0.00023863293,"threshold_uncertainty_score":0.0147538185},"labels":[],"label_agreement":null},{"id":"W4320485436","doi":"10.1038/s41588-023-01334-w","title":"Author Correction: Deciphering colorectal cancer genetics through multi-omic analysis of 100,204 cases and 154,587 controls of European and east Asian ancestries","year":2023,"lang":"en","type":"erratum","venue":"Nature Genetics","topic":"Genetic factors in colorectal cancer","field":"Medicine","cited_by":4,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Memorial University of Newfoundland; Lunenfeld-Tanenbaum Research Institute; Ontario Institute for Cancer Research; University of Toronto; Mount Sinai Hospital","funders":"Medical Research Council; Cancer Research UK; World Health Organization","keywords":"Biology; Colorectal cancer; Computational biology; Genetics; Cancer genetics; Cancer","score_opus":0.037555321858831446,"score_gpt":0.33399182457458826,"score_spread":0.29643650271575683,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4320485436","genre_codex":"editorial","genre_gemma":"other","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"other","genre_consensus":null,"domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.0003146328,0.00055558217,0.0007797053,0.04689537,0.94856673,0.000024174273,0.0013300647,0.00029938898,0.0012343491],"genre_scores_gemma":[0.039432105,0.007015267,0.015435245,0.20573117,0.47782066,0.00042316475,0.0064932615,0.004046295,0.24360287],"study_design_codex":"not_applicable","study_design_gemma":"not_applicable","domain_scores_codex":[0.99478984,0.0009935936,0.0009075877,0.0007584691,0.0020431313,0.0005073899],"domain_scores_gemma":[0.9678467,0.009761792,0.0016491384,0.0022711016,0.016584713,0.0018864246],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0062535354,0.002433825,0.0022950843,0.0037932682,0.0034509825,0.003365966,0.004286628,0.0073993467,0.0394315],"category_scores_gemma":[0.071438886,0.0014500024,0.0019851613,0.0021604102,0.002207272,0.0016077214,0.0022809217,0.01116141,0.01952127],"study_design_candidate":"not_applicable","study_design_consensus":"not_applicable","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.000038322996,0.0000065176646,0.00016694938,0.00010682396,0.000026764788,0.000601242,0.000036558264,0.000034114706,0.000048838778,0.00030969552,0.99600536,0.0026187357],"study_design_scores_gemma":[0.0002456034,0.000046148223,0.00206856,0.00073425943,0.0002638989,0.0034857104,0.0002143448,0.00064891303,0.00078764244,0.0020827868,0.9893399,0.00008244041],"about_ca_topic_score_codex":0.022126582,"about_ca_topic_score_gemma":0.02667711,"teacher_disagreement_score":0.0394315,"about_ca_system_score_codex":0.0039444924,"about_ca_system_score_gemma":0.005920331,"threshold_uncertainty_score":0.13191158},"labels":[],"label_agreement":null},{"id":"W4321613865","doi":"10.1038/s41588-023-01336-8","title":"Author Correction: Discovery of 42 genome-wide significant loci associated with dyslexia","year":2023,"lang":"en","type":"erratum","venue":"Nature Genetics","topic":"Education Methods and Practices","field":"Social Sciences","cited_by":0,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Université du Québec à Chicoutimi; Université de Montréal; Centre Hospitalier Universitaire Sainte-Justine; Hospital for Sick Children; University of Toronto; University Health Network","funders":"National Center for Advancing Translational Sciences; National Health and Medical Research Council; National Natural Science Foundation of China; Waterloo Foundation","keywords":"Biology; Dyslexia; Genetics; Computational biology; Genome; Genome-wide association study; Evolutionary biology; Gene; Reading (process); Single-nucleotide polymorphism; Genotype; Linguistics","score_opus":0.04007733669623777,"score_gpt":0.37501224322329835,"score_spread":0.3349349065270606,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4321613865","genre_codex":"editorial","genre_gemma":"other","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"other","genre_consensus":null,"domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.0002608335,0.00047012488,0.0024704526,0.043382715,0.9453272,0.000037843834,0.0037219354,0.0010748968,0.0032538755],"genre_scores_gemma":[0.031357106,0.004307344,0.025280612,0.13204212,0.27760065,0.000692149,0.014930221,0.010645931,0.5031438],"study_design_codex":"not_applicable","study_design_gemma":"not_applicable","domain_scores_codex":[0.994017,0.0010640913,0.0010857354,0.0009883692,0.0024893305,0.00035533414],"domain_scores_gemma":[0.95646214,0.014946423,0.0018968729,0.0032901813,0.022083988,0.0013204305],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.006339201,0.0023732923,0.001768734,0.004175073,0.0027942013,0.0026452974,0.0032216008,0.004134628,0.12139714],"category_scores_gemma":[0.08877777,0.0011993552,0.0017951209,0.00260039,0.0016447259,0.0016162466,0.0021972624,0.009248318,0.050839644],"study_design_candidate":"not_applicable","study_design_consensus":"not_applicable","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.000030955853,0.0000037121467,0.00008628955,0.00008326145,0.000014384143,0.00017261934,0.00003036788,0.000028148661,0.000053690364,0.00043288202,0.99494064,0.004122956],"study_design_scores_gemma":[0.00013207782,0.000021523312,0.0015486288,0.0005849407,0.0001104378,0.0013647162,0.000116334064,0.0005006268,0.00079396105,0.003162238,0.99159765,0.000066919994],"about_ca_topic_score_codex":0.018721005,"about_ca_topic_score_gemma":0.027530573,"teacher_disagreement_score":0.12139714,"about_ca_system_score_codex":0.0031918248,"about_ca_system_score_gemma":0.0046164645,"threshold_uncertainty_score":0.40611386},"labels":[],"label_agreement":null},{"id":"W4322492208","doi":"10.1038/s41588-023-01320-2","title":"Multiomic analysis of homologous recombination-deficient end-stage high-grade serous ovarian cancer","year":2023,"lang":"en","type":"article","venue":"Nature Genetics","topic":"DNA Repair Mechanisms","field":"Biochemistry, Genetics and Molecular Biology","cited_by":86,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Victoria; University of British Columbia","funders":"U.S. Department of Defense","keywords":"Biology; Serous ovarian cancer; Homologous recombination; Serous fluid; Ovarian cancer; Homologous chromosome; Recombination; Genetics; Cancer research; Cancer; Gene; Biochemistry","score_opus":0.009760388653085882,"score_gpt":0.277840759652048,"score_spread":0.26808037099896215,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4322492208","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99734145,0.00024324785,0.0011729747,0.000025373101,0.000008170281,0.000013218025,0.00071052357,0.000020311067,0.00046472173],"genre_scores_gemma":[0.996992,0.00016033305,0.00070580386,0.000024418778,0.0000027260178,0.000011894397,0.0010006512,0.000014447903,0.0010877659],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9999089,0.000010248647,0.0000059224076,0.000019176488,0.000026162654,0.00002954107],"domain_scores_gemma":[0.9999007,0.00001858568,0.000027129186,0.000011331508,0.000015297135,0.000026923919],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00009003949,0.00014668395,0.0001824066,0.00055049174,0.00016499951,0.00022698904,0.000113801914,0.00015489949,0.0011358762],"category_scores_gemma":[0.00013742289,0.000088426204,0.00022866685,0.0003126349,0.00011016529,0.000073399795,0.00018382014,0.00018930344,0.00018335329],"study_design_candidate":"bench_or_experimental","study_design_consensus":"bench_or_experimental","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00019071657,0.000014373153,0.0021314002,0.000011289087,0.000009604251,0.000109745044,0.000017687746,0.000031914522,0.996567,0.00004471623,0.000027759144,0.0008436847],"study_design_scores_gemma":[0.000050375118,0.00062472286,0.35287726,0.000008124822,0.00014869763,0.002644589,0.00028402914,0.0026320824,0.6345516,0.00016072068,0.0060044876,0.000013355043],"about_ca_topic_score_codex":0.0008145525,"about_ca_topic_score_gemma":0.0010361775,"teacher_disagreement_score":0.0011358762,"about_ca_system_score_codex":0.00014939927,"about_ca_system_score_gemma":0.00011103621,"threshold_uncertainty_score":0.0037999153},"labels":[],"label_agreement":null},{"id":"W4322734715","doi":"10.1038/s41588-023-01350-w","title":"Author Correction: Genome-wide analyses of ADHD identify 27 risk loci, refine the genetic architecture and implicate several cognitive domains","year":2023,"lang":"en","type":"erratum","venue":"Nature Genetics","topic":"Attention Deficit Hyperactivity Disorder","field":"Medicine","cited_by":15,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Hospital for Sick Children; Douglas Mental Health University Institute; McGill University","funders":"","keywords":"Biology; Genetic architecture; Computational biology; Genome-wide association study; Cognition; Genetics; Genome; Evolutionary biology; Quantitative trait locus; Neuroscience; Gene; Single-nucleotide polymorphism; Genotype","score_opus":0.045402036031950234,"score_gpt":0.37680659775804853,"score_spread":0.3314045617260983,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4322734715","genre_codex":"editorial","genre_gemma":"other","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"other","genre_consensus":null,"domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.000294148,0.00055082317,0.001224529,0.053022817,0.9389548,0.00003645428,0.0028287033,0.0006827123,0.0024049676],"genre_scores_gemma":[0.04217687,0.0062231016,0.020907415,0.14508736,0.4105229,0.0005614415,0.011815117,0.006472841,0.356233],"study_design_codex":"not_applicable","study_design_gemma":"not_applicable","domain_scores_codex":[0.9959572,0.0006306888,0.00075366325,0.00075825845,0.0014409795,0.00045919418],"domain_scores_gemma":[0.97631943,0.0067442874,0.0015278124,0.0016651617,0.012279889,0.0014634249],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.004045827,0.0026425929,0.002554901,0.003597966,0.0038151466,0.0035618742,0.0052273683,0.008373692,0.11995797],"category_scores_gemma":[0.06255246,0.0016859977,0.0021227065,0.0023949472,0.0023651607,0.0020721606,0.00230183,0.011887221,0.03203015],"study_design_candidate":"not_applicable","study_design_consensus":"not_applicable","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00005999508,0.000006727821,0.00019964954,0.00013725038,0.00003393769,0.0007163683,0.0000375791,0.00005109262,0.00007075859,0.00076072296,0.99380964,0.004116353],"study_design_scores_gemma":[0.0004696175,0.000046978526,0.0034211783,0.00095035805,0.00029024377,0.0051751835,0.0002327506,0.0008693238,0.0009879041,0.006399324,0.981016,0.00014119892],"about_ca_topic_score_codex":0.025547123,"about_ca_topic_score_gemma":0.038870007,"teacher_disagreement_score":0.11995797,"about_ca_system_score_codex":0.0035163872,"about_ca_system_score_gemma":0.0062811603,"threshold_uncertainty_score":0.40129936},"labels":[],"label_agreement":null},{"id":"W4323667295","doi":"10.1038/s41588-023-01330-0","title":"Identifying individuals at extreme risk of venous thromboembolism using polygenic risk scores","year":2023,"lang":"en","type":"letter","venue":"Nature Genetics","topic":"Blood Coagulation and Thrombosis Mechanisms","field":"Medicine","cited_by":1,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Thrombosis and Atherosclerosis Research Institute; McMaster University; Population Health Research Institute","funders":"","keywords":"Venous thromboembolism; Polygenic risk score; Biology; Complement (music); Risk assessment; Thrombophilia; Genetic testing; Intensive care medicine; Bioinformatics; Internal medicine; Genetics; Medicine; Gene; Thrombosis; Single-nucleotide polymorphism; Phenotype; Computer science; Genotype","score_opus":0.06349728824989019,"score_gpt":0.3164999624547785,"score_spread":0.2530026742048883,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4323667295","genre_codex":"commentary","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":null,"domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.035596963,0.0022233445,0.002637745,0.9400334,0.009787457,0.000049273265,0.00032958813,0.00008311951,0.009259079],"genre_scores_gemma":[0.33819413,0.0035319838,0.0072815293,0.5676359,0.07247688,0.00018523063,0.0002627346,0.000078228324,0.010353375],"study_design_codex":"not_applicable","study_design_gemma":"observational","domain_scores_codex":[0.9983072,0.00095159106,0.00015072047,0.00017914173,0.00028602098,0.00012541449],"domain_scores_gemma":[0.99308807,0.0052927374,0.0002529253,0.0002419002,0.0005894182,0.000534983],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0019862491,0.00055832986,0.0010347693,0.0007661701,0.001154473,0.0013574363,0.00063485024,0.009338965,0.0021219603],"category_scores_gemma":[0.018774629,0.00031709464,0.0005120326,0.0007109193,0.00095171743,0.00090178096,0.0004954488,0.0077096643,0.0012104511],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0012677063,0.00051038916,0.21473105,0.00020820611,0.00046865095,0.034550313,0.001202312,0.0011041231,0.002927862,0.01050136,0.5348344,0.19769368],"study_design_scores_gemma":[0.0023850854,0.0018704047,0.21165663,0.0013605609,0.0014204233,0.122329146,0.0037829652,0.041339844,0.0037589173,0.18294758,0.42666772,0.0004807442],"about_ca_topic_score_codex":0.0027688227,"about_ca_topic_score_gemma":0.004338016,"teacher_disagreement_score":0.009338965,"about_ca_system_score_codex":0.0006723285,"about_ca_system_score_gemma":0.00066416466,"threshold_uncertainty_score":0.010504425},"labels":[],"label_agreement":null},{"id":"W4324044597","doi":"10.1038/s41588-023-01305-1","title":"Schizophrenia risk conferred by rare protein-truncating variants is conserved across diverse human populations","year":2023,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Genetic Associations and Epidemiology","field":"Biochemistry, Genetics and Molecular Biology","cited_by":73,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Centre for Addiction and Mental Health; University of British Columbia; Queen's University","funders":"NIH Clinical Center; National Institute on Drug Abuse; National Institute of Mental Health; National Institute on Aging; European Regional Development Fund; Instituto de Salud Carlos III; National Health and Medical Research Council; SUNY Downstate Medical Center; Graduate School of Public Health, University of Pittsburgh; National Institutes of Health; State University of New York; University of Peshawar; Sorbonne Université; Australian Schizophrenia Research Bank; Medical Research Council; Università degli Studi di Brescia; Instituto de Investigación Sanitaria Gregorio Marañón; Innovative Medicines Initiative; European Commission; Universita degli Studi di Bari Aldo Moro; Queen's University; Institut National de la Santé et de la Recherche Médicale; Ministero della Salute; Universität Wien; Queensland Brain Institute; Karolinska Institutet; University of Queensland; Monash University; University of North Carolina at Chapel Hill; University of Wollongong; Cardiff University; Neuroscience Research Australia; Università degli Studi di Trento; Virginia Commonwealth University; University of New South Wales; University of Pittsburgh; Ministerio de Ciencia e Innovación; Johns Hopkins University; Centro de Investigación Biomédica en Red de Salud Mental; Feinstein Institutes for Medical Research; Fundación Alicia Koplowitz; F. Hoffmann-La Roche; Helsingin Yliopisto; Microsoft Research; Stanley Center for Psychiatric Research, Broad Institute; U.S. Department of Veterans Affairs; University of Pennsylvania; Broad Institute; Universidad de Granada; Medizinische Universität Wien; McLean Hospital; Massachusetts General Hospital; University College London; Brigham and Women's Hospital; Northwell Health; U.S. Department of Health and Human Services","keywords":"Biology; Genetics; Gene; Allele; Genetic architecture; 1000 Genomes Project; Genome-wide association study; Human genome; Allele frequency; Schizophrenia (object-oriented programming); Genome; Evolutionary biology; Computational biology; Single-nucleotide polymorphism; Phenotype; Genotype; Medicine","score_opus":0.026450512125677554,"score_gpt":0.3255666805153204,"score_spread":0.29911616838964283,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4324044597","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9954354,0.0018534057,0.0013195287,0.000117315765,0.000019194644,0.000010501669,0.00073392456,0.00003143255,0.0004791715],"genre_scores_gemma":[0.99895096,0.00041796677,0.00023807955,0.00003810403,0.000012475047,0.0000051681823,0.00028721165,0.000007915794,0.000042033116],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99833846,0.000514014,0.00017645606,0.0006424152,0.00021377875,0.0001147939],"domain_scores_gemma":[0.9983367,0.0005735143,0.00054528716,0.00032452826,0.000090251044,0.00012974377],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0016656949,0.0006213218,0.0007378289,0.0016217189,0.0007670091,0.001067045,0.0004367016,0.00062280573,0.0020614003],"category_scores_gemma":[0.0033355118,0.0003283015,0.0012175959,0.0016721324,0.00075209857,0.0003254591,0.00096811017,0.00055929815,0.00018184206],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0020112821,0.000056011435,0.9552816,0.00019133078,0.0069825165,0.0015322566,0.00044800367,0.0011157317,0.018465681,0.0005273,0.00039719878,0.0129910465],"study_design_scores_gemma":[0.000102920756,0.0002324971,0.99079555,0.00006323396,0.0021904798,0.0016752377,0.00029561666,0.0012094764,0.0012183447,0.0013071834,0.0008809052,0.000028566816],"about_ca_topic_score_codex":0.0044158935,"about_ca_topic_score_gemma":0.0042260895,"teacher_disagreement_score":0.0044158935,"about_ca_system_score_codex":0.00022701261,"about_ca_system_score_gemma":0.00023566505,"threshold_uncertainty_score":0.008809149},"labels":[],"label_agreement":null},{"id":"W4324045235","doi":"10.1038/s41588-023-01314-0","title":"Multi-ancestry genome-wide association analyses improve resolution of genes and pathways influencing lung function and chronic obstructive pulmonary disease risk","year":2023,"lang":"en","type":"review","venue":"Nature Genetics","topic":"Chronic Obstructive Pulmonary Disease (COPD) Research","field":"Medicine","cited_by":186,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"McGill University","funders":"National Institute of Environmental Health Sciences; National Heart, Lung, and Blood Institute; NIHR Leicester Biomedical Research Centre; NIHR Nottingham Biomedical Research Centre; School of Public Health, Imperial College London; Institute of Genetics; National Health and Medical Research Council; Wellcome Trust; Cancer Research UK; BHF Centre of Research Excellence, Oxford; Biotechnology and Biological Sciences Research Council; MRC-PHE Centre for Environment and Health; Universiteit Gent; British Lung Foundation; University of Oxford; National Institutes of Health; University of Leicester; Alpha-1 Foundation; National Institute for Health and Care Research; Peking University; Brigham and Women's Hospital; British Heart Foundation; UK Research and Innovation; Universität Basel; National Cancer Institute; University of Bristol; COPD Foundation; Medical Research Council; University of Texas Health Science Center at Houston; Imperial College London; Peking University Health Science Center; Wellcome","keywords":"Phenome; Genome-wide association study; Biology; COPD; Genetic association; Gene; Disease; Genetics; Lung function; Genome; Bioinformatics; Computational biology; Single-nucleotide polymorphism; Lung; Genotype; Medicine; Internal medicine","score_opus":0.04291628776939022,"score_gpt":0.3508168932087169,"score_spread":0.3079006054393267,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4324045235","genre_codex":"review","genre_gemma":"review","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"review","genre_consensus":"review","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.00012519248,0.9989617,0.00017585469,0.0002786769,0.000065376684,0.0000040208956,0.000036869093,0.000007646323,0.0003446805],"genre_scores_gemma":[0.0018581903,0.997059,0.00047454645,0.00024861432,0.000071950635,0.0000074445898,0.000086169166,0.0000029348284,0.00019113692],"study_design_codex":"design_other","study_design_gemma":"meta_analysis","domain_scores_codex":[0.9994592,0.00017729128,0.000070590824,0.0000945135,0.00015062436,0.000047905247],"domain_scores_gemma":[0.99821657,0.0012596357,0.00015774682,0.000048569724,0.00024756967,0.00006991066],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0019201583,0.0009280368,0.0025812984,0.0031387915,0.00020322808,0.0011132371,0.001190554,0.0011570504,0.0038841723],"category_scores_gemma":[0.0027817225,0.00028091393,0.0017188935,0.002942852,0.00041382507,0.0010214566,0.00087253464,0.0018789081,0.0011536161],"study_design_candidate":"meta_analysis","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00026404698,0.000047874946,0.0010272037,0.045282472,0.0019651728,0.00017028122,0.000046390483,0.0005324174,0.0011913944,0.0037134872,0.013606669,0.93215257],"study_design_scores_gemma":[0.00016876463,0.00027140114,0.011733461,0.028237527,0.0062914006,0.001833689,0.0001464165,0.00052073173,0.00095251267,0.011316284,0.9384492,0.00007861715],"about_ca_topic_score_codex":0.0015660505,"about_ca_topic_score_gemma":0.003708107,"teacher_disagreement_score":0.0038841723,"about_ca_system_score_codex":0.00070876814,"about_ca_system_score_gemma":0.0016747334,"threshold_uncertainty_score":0.012993813},"labels":[],"label_agreement":null},{"id":"W4324129655","doi":"10.1038/s41588-023-01298-x","title":"Preneoplastic stromal cells promote BRCA1-mediated breast tumorigenesis","year":2023,"lang":"en","type":"article","venue":"Nature Genetics","topic":"BRCA gene mutations in cancer","field":"Biochemistry, Genetics and Molecular Biology","cited_by":63,"is_retracted":false,"has_abstract":false,"route_ca_aff":false,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"","funders":"Congressionally Directed Medical Research Programs; Division of Cancer Epidemiology and Genetics, National Cancer Institute; National Institute of General Medical Sciences; University of California, Irvine; Chao Family Comprehensive Cancer Center; U.S. Department of Defense; Breast Cancer Research Foundation; National Cancer Institute; U.S. Department of Health and Human Services; National Institutes of Health; Canadian Institutes of Health Research; National Science Foundation; California Institute for Regenerative Medicine; American Cancer Society","keywords":"Biology; Stromal cell; Carcinogenesis; Cancer research; Paracrine signalling; Progenitor cell; Epithelium; Breast cancer; Stem cell; Cell biology; Cancer; Genetics","score_opus":0.005508753235700718,"score_gpt":0.24803275923644727,"score_spread":0.24252400600074656,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4324129655","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.971101,0.004013749,0.006411085,0.00048124514,0.000119984026,0.00010207638,0.0015066079,0.00061913667,0.015645176],"genre_scores_gemma":[0.98634213,0.0013854477,0.0012751579,0.00009536206,0.000024129062,0.00003240801,0.00051275553,0.000048653157,0.010283944],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.999863,0.000033364777,0.0000070235806,0.000015998581,0.000039239,0.00004134654],"domain_scores_gemma":[0.9997181,0.00008692395,0.00003733543,0.000042644297,0.000030266137,0.00008473506],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00017047797,0.0002987569,0.00017900886,0.000485781,0.00017611244,0.00036290806,0.00014174994,0.0002610208,0.004925868],"category_scores_gemma":[0.00017192314,0.00023251497,0.00017746232,0.0001948724,0.0001915856,0.0002417753,0.00038435106,0.0006225817,0.0011547557],"study_design_candidate":"bench_or_experimental","study_design_consensus":"bench_or_experimental","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0001530472,0.000038636645,0.00028303172,0.000028329707,0.000002646777,0.00013594511,0.000020644862,0.00006420863,0.9974712,0.00034040108,0.000112338894,0.001349635],"study_design_scores_gemma":[0.0000145933045,0.00015342789,0.004617052,0.0000048345055,0.0000051067327,0.00045034685,0.000056113156,0.00038118736,0.98934656,0.00014485988,0.0048232623,0.0000026799694],"about_ca_topic_score_codex":0.0008608092,"about_ca_topic_score_gemma":0.0013353111,"teacher_disagreement_score":0.004925868,"about_ca_system_score_codex":0.00023723638,"about_ca_system_score_gemma":0.00022888303,"threshold_uncertainty_score":0.016478717},"labels":[],"label_agreement":null},{"id":"W4353015145","doi":"10.1038/s41588-023-01316-y","title":"Author Correction: The landscape of viral associations in human cancers","year":2023,"lang":"en","type":"erratum","venue":"Nature Genetics","topic":"Cancer Immunotherapy and Biomarkers","field":"Medicine","cited_by":1,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"SickKids Foundation; BC Cancer Agency; University of British Columbia; Prostate Cancer Canada; Simon Fraser University; University of Ottawa; McGill University; Lunenfeld-Tanenbaum Research Institute; Mount Sinai Hospital; Princess Margaret Cancer Centre; University of Calgary; Vector Institute; University of Toronto; McGill University and Génome Québec Innovation Centre; Toronto General Hospital; University Health Network; Genome Canada; Canada's Michael Smith Genome Sciences Centre; Hospital for Sick Children; Université de Montréal; Institute of Cancer Research; Ontario Institute for Cancer Research","funders":"Medical Research Council; Cancer Research UK","keywords":"Biology; Computational biology; Evolutionary biology; Virology; Genetics","score_opus":0.01618637235036813,"score_gpt":0.31752070353098266,"score_spread":0.30133433118061453,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4353015145","genre_codex":"editorial","genre_gemma":"other","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"other","genre_consensus":null,"domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.00023593279,0.00092150975,0.0017060196,0.055802416,0.93617874,0.00002188189,0.001547784,0.0005965646,0.0029891476],"genre_scores_gemma":[0.030480888,0.011062514,0.019729838,0.1619056,0.46214992,0.0003255428,0.007990809,0.0063213445,0.30003348],"study_design_codex":"not_applicable","study_design_gemma":"not_applicable","domain_scores_codex":[0.9924412,0.0013323923,0.0012119561,0.001362394,0.003145106,0.0005070481],"domain_scores_gemma":[0.9507238,0.013629083,0.002331301,0.00431043,0.027073564,0.0019317187],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.006856342,0.0017990189,0.0013121582,0.0034795913,0.0029695483,0.0048722033,0.00311151,0.00509955,0.04612145],"category_scores_gemma":[0.096253365,0.00092904054,0.0015983826,0.002629551,0.0021976628,0.0024891933,0.0023540838,0.0114591615,0.030519275],"study_design_candidate":"not_applicable","study_design_consensus":"not_applicable","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.000025474259,0.0000036758943,0.00011516941,0.000077636076,0.000013508623,0.00017734978,0.000041446954,0.0000348439,0.000055624292,0.0008104042,0.9930896,0.0055553126],"study_design_scores_gemma":[0.00003208331,0.000011634508,0.0005855378,0.00034391295,0.00004978429,0.0009970859,0.00009292116,0.00021217517,0.000515047,0.0022242405,0.9948986,0.000037035163],"about_ca_topic_score_codex":0.011054495,"about_ca_topic_score_gemma":0.0126688965,"teacher_disagreement_score":0.04612145,"about_ca_system_score_codex":0.003141807,"about_ca_system_score_gemma":0.005928885,"threshold_uncertainty_score":0.15429163},"labels":[],"label_agreement":null},{"id":"W4353015523","doi":"10.1038/s41588-023-01315-z","title":"Author Correction: Comprehensive analysis of chromothripsis in 2,658 human cancers using whole-genome sequencing","year":2023,"lang":"en","type":"erratum","venue":"Nature Genetics","topic":"Cancer Genomics and Diagnostics","field":"Biochemistry, Genetics and Molecular Biology","cited_by":5,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"SickKids Foundation; BC Cancer Agency; University of British Columbia; Prostate Cancer Canada; Université de Montréal; Hospital for Sick Children; Simon Fraser University; University of Ottawa; McGill University; Lunenfeld-Tanenbaum Research Institute; Mount Sinai Hospital; Princess Margaret Cancer Centre; University of Calgary; University of Toronto; McGill University and Génome Québec Innovation Centre; Toronto General Hospital; University Health Network; Genome Canada; Canada's Michael Smith Genome Sciences Centre; Vector Institute; Institute of Cancer Research; Ontario Institute for Cancer Research","funders":"Medical Research Council; National Institute for Health and Care Research; Cancer Research UK","keywords":"Chromothripsis; Biology; Computational biology; Human genome; Genome; Genetics; Cancer genome sequencing; Gene; DNA; Genome instability","score_opus":0.02580379894199993,"score_gpt":0.31234496428180386,"score_spread":0.28654116533980395,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4353015523","genre_codex":"editorial","genre_gemma":"other","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"other","genre_consensus":null,"domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.0005420045,0.00083620014,0.0040804376,0.044420443,0.9409003,0.000036355417,0.00342583,0.0011646083,0.004593878],"genre_scores_gemma":[0.03866527,0.010035502,0.04654338,0.13934489,0.2460453,0.00038005976,0.019774694,0.00979781,0.48941308],"study_design_codex":"not_applicable","study_design_gemma":"not_applicable","domain_scores_codex":[0.9952785,0.0005219941,0.00071314926,0.0008066242,0.0023992932,0.0002805209],"domain_scores_gemma":[0.97074705,0.0074572414,0.0013261156,0.0022855496,0.017004406,0.0011796391],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.004230822,0.0016655067,0.0013183614,0.0028673739,0.0027353158,0.0029573038,0.0029649297,0.0041803555,0.04960735],"category_scores_gemma":[0.05143968,0.0009457474,0.0011733918,0.0023877567,0.0016454464,0.0017519873,0.0021528783,0.010009856,0.02964098],"study_design_candidate":"not_applicable","study_design_consensus":"not_applicable","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.000032060445,0.0000071231534,0.00015219128,0.00009918568,0.000016032263,0.00045204692,0.000037748418,0.000059507238,0.0001761474,0.0007603547,0.9899491,0.008258509],"study_design_scores_gemma":[0.000042241296,0.000014526043,0.0008991518,0.00028206923,0.00005713781,0.0019241276,0.000075319345,0.00030369012,0.0011067927,0.0018000656,0.99344975,0.000045178054],"about_ca_topic_score_codex":0.01166527,"about_ca_topic_score_gemma":0.017364897,"teacher_disagreement_score":0.04960735,"about_ca_system_score_codex":0.00246268,"about_ca_system_score_gemma":0.004417028,"threshold_uncertainty_score":0.1659531},"labels":[],"label_agreement":null},{"id":"W4353015909","doi":"10.1038/s41588-023-01319-9","title":"Author Correction: Pan-cancer analysis of whole genomes identifies driver rearrangements promoted by LINE-1 retrotransposition","year":2023,"lang":"en","type":"erratum","venue":"Nature Genetics","topic":"Chromosomal and Genetic Variations","field":"Agricultural and Biological Sciences","cited_by":5,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":true,"ca_institutions":"SickKids Foundation; BC Cancer Agency; University of British Columbia; Prostate Cancer Canada; Université de Montréal; Hospital for Sick Children; Genome Canada; Canada's Michael Smith Genome Sciences Centre; Vector Institute; Simon Fraser University; McGill University; University of Ottawa; Institute of Cancer Research; Ontario Institute for Cancer Research; University of Toronto; McGill University and Génome Québec Innovation Centre; Toronto General Hospital; University Health Network; Lunenfeld-Tanenbaum Research Institute; Mount Sinai Hospital; Princess Margaret Cancer Centre; University of Calgary","funders":"Medical Research Council; Cancer Research UK","keywords":"Retrotransposon; Biology; Genome; Genetics; Computational biology; Line (geometry); Cancer; Gene; Transposable element","score_opus":0.016832346457663374,"score_gpt":0.2698774081425745,"score_spread":0.25304506168491114,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4353015909","genre_codex":"editorial","genre_gemma":"other","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"other","genre_consensus":null,"domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.0005058741,0.00070508855,0.0036237764,0.039049726,0.94845724,0.000028286477,0.0023987899,0.0010046237,0.0042266985],"genre_scores_gemma":[0.049029052,0.0102117155,0.041594654,0.13867797,0.26698405,0.00036722716,0.014755586,0.010454133,0.46792567],"study_design_codex":"not_applicable","study_design_gemma":"not_applicable","domain_scores_codex":[0.99591655,0.000524993,0.00070598116,0.0007696106,0.0018067007,0.00027621267],"domain_scores_gemma":[0.9745155,0.007225189,0.0012548785,0.0020978036,0.013909694,0.0009969765],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0034518633,0.0017032552,0.0012166515,0.0028406992,0.002888231,0.003083295,0.002850506,0.005049552,0.0546171],"category_scores_gemma":[0.05450476,0.00095046195,0.0012613775,0.0023439785,0.0016949421,0.00175959,0.0019252873,0.009767886,0.03018811],"study_design_candidate":"not_applicable","study_design_consensus":"not_applicable","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.000046099165,0.000008888081,0.00018121768,0.00012259488,0.000018701607,0.00064811716,0.000060357957,0.000075868236,0.00020488001,0.0011337389,0.98801684,0.009482655],"study_design_scores_gemma":[0.000038699156,0.000016047308,0.0007464724,0.00025485046,0.000052383282,0.0020208694,0.00009120772,0.00032371952,0.0009808264,0.0018923982,0.9935408,0.000041780724],"about_ca_topic_score_codex":0.011529182,"about_ca_topic_score_gemma":0.014709368,"teacher_disagreement_score":0.0546171,"about_ca_system_score_codex":0.0022867804,"about_ca_system_score_gemma":0.003745538,"threshold_uncertainty_score":0.18271244},"labels":[],"label_agreement":null},{"id":"W4353016752","doi":"10.1038/s41588-023-01317-x","title":"Author Correction: Comprehensive molecular characterization of mitochondrial genomes in human cancers","year":2023,"lang":"en","type":"erratum","venue":"Nature Genetics","topic":"Mitochondrial Function and Pathology","field":"Biochemistry, Genetics and Molecular Biology","cited_by":2,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"SickKids Foundation; BC Cancer Agency; University of British Columbia; Prostate Cancer Canada; Université de Montréal; Hospital for Sick Children; Lunenfeld-Tanenbaum Research Institute; Mount Sinai Hospital; University of Calgary; Princess Margaret Cancer Centre; Simon Fraser University; University of Ottawa; McGill University; Vector Institute; University of Toronto; McGill University and Génome Québec Innovation Centre; Toronto General Hospital; University Health Network; Genome Canada; Canada's Michael Smith Genome Sciences Centre; Institute of Cancer Research; Ontario Institute for Cancer Research","funders":"Medical Research Council; Cancer Research UK","keywords":"Biology; Computational biology; Genome; Mitochondrial DNA; Genetics; Human genome; Evolutionary biology; Gene","score_opus":0.012411858973637613,"score_gpt":0.2793280363473929,"score_spread":0.2669161773737553,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4353016752","genre_codex":"editorial","genre_gemma":"other","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"other","genre_consensus":null,"domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.0003179307,0.0007797595,0.0028786613,0.041223146,0.94735694,0.000028232089,0.002093346,0.00087649736,0.0044454597],"genre_scores_gemma":[0.03251179,0.01136954,0.035618864,0.11919771,0.30332205,0.00033619933,0.013657768,0.008474517,0.47551158],"study_design_codex":"not_applicable","study_design_gemma":"not_applicable","domain_scores_codex":[0.9944061,0.0006831923,0.00090886914,0.00086427416,0.002802344,0.0003352654],"domain_scores_gemma":[0.96117765,0.008969097,0.0015378942,0.0029426634,0.024016345,0.001356346],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0042415005,0.0018140742,0.0013792469,0.0034305004,0.003070876,0.0034427454,0.0032500392,0.0045579826,0.04723678],"category_scores_gemma":[0.060264297,0.0009869138,0.0013133948,0.00260766,0.0018524273,0.0021830488,0.0022281935,0.011413878,0.0324745],"study_design_candidate":"not_applicable","study_design_consensus":"not_applicable","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.000027999646,0.0000069367793,0.0001036704,0.00008650207,0.000011946766,0.0003187647,0.000033293523,0.00005916952,0.00011633699,0.0009344646,0.9907832,0.007517602],"study_design_scores_gemma":[0.000029942436,0.000012170452,0.00066293654,0.00027079557,0.00004172021,0.0014422294,0.00006432246,0.0002710746,0.0009038079,0.002075819,0.99418455,0.00004050883],"about_ca_topic_score_codex":0.012824292,"about_ca_topic_score_gemma":0.017593598,"teacher_disagreement_score":0.04723678,"about_ca_system_score_codex":0.0028768145,"about_ca_system_score_gemma":0.0046514855,"threshold_uncertainty_score":0.15802276},"labels":[],"label_agreement":null},{"id":"W4353020465","doi":"10.1038/s41588-023-01318-w","title":"Author Correction: Disruption of chromatin folding domains by somatic genomic rearrangements in human cancer","year":2023,"lang":"en","type":"erratum","venue":"Nature Genetics","topic":"Cancer Genomics and Diagnostics","field":"Biochemistry, Genetics and Molecular Biology","cited_by":1,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"SickKids Foundation; BC Cancer Agency; University of British Columbia; Prostate Cancer Canada; Université de Montréal; Hospital for Sick Children; Simon Fraser University; University of Ottawa; McGill University; Lunenfeld-Tanenbaum Research Institute; Mount Sinai Hospital; Princess Margaret Cancer Centre; University of Calgary; University of Toronto; McGill University and Génome Québec Innovation Centre; Toronto General Hospital; University Health Network; Genome Canada; Canada's Michael Smith Genome Sciences Centre; Vector Institute; Institute of Cancer Research; Ontario Institute for Cancer Research","funders":"Medical Research Council; Cancer Research UK","keywords":"Biology; Chromatin; Somatic cell; Folding (DSP implementation); Computational biology; Genetics; Evolutionary biology; DNA; Gene","score_opus":0.009891885674141291,"score_gpt":0.3016454026782409,"score_spread":0.2917535170040996,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4353020465","genre_codex":"editorial","genre_gemma":"other","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"other","genre_consensus":null,"domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.00054891064,0.0008529985,0.003669947,0.041731104,0.943669,0.000027840846,0.0020067242,0.0010335654,0.006459972],"genre_scores_gemma":[0.042204812,0.00974484,0.03410867,0.08480829,0.18803108,0.00024520888,0.0103887515,0.008324708,0.6221436],"study_design_codex":"not_applicable","study_design_gemma":"not_applicable","domain_scores_codex":[0.9959162,0.00045483024,0.000629885,0.00068613293,0.00206414,0.0002488236],"domain_scores_gemma":[0.978961,0.005226779,0.0009007191,0.0015976798,0.012480108,0.00083368464],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0029611248,0.0016008142,0.0012302111,0.0023503967,0.0029202867,0.0029000484,0.0028505288,0.0043155462,0.04938561],"category_scores_gemma":[0.038068052,0.0008046558,0.0010927374,0.0019007274,0.0015962715,0.0017590735,0.0019060884,0.009021814,0.028427886],"study_design_candidate":"not_applicable","study_design_consensus":"not_applicable","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.000043812484,0.00000956652,0.00013625383,0.00010952741,0.000015606885,0.00069635996,0.00004614331,0.000094914445,0.00024204497,0.0014284693,0.98677164,0.010405704],"study_design_scores_gemma":[0.00002685703,0.00001193237,0.0006101007,0.00021359029,0.00003937429,0.0018416322,0.00006785403,0.00031957132,0.0015427469,0.002045979,0.9932428,0.000037490143],"about_ca_topic_score_codex":0.009267124,"about_ca_topic_score_gemma":0.014637243,"teacher_disagreement_score":0.04938561,"about_ca_system_score_codex":0.002402477,"about_ca_system_score_gemma":0.003269627,"threshold_uncertainty_score":0.16521132},"labels":[],"label_agreement":null},{"id":"W4362523789","doi":"10.1038/s41588-023-01343-9","title":"Genetic effects on the timing of parturition and links to fetal birth weight","year":2023,"lang":"en","type":"review","venue":"Nature Genetics","topic":"Preterm Birth and Chorioamnionitis","field":"Medicine","cited_by":95,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Centre Intégré Universitaire de Santé et de Services Sociaux du Saguenay–Lac-Saint-Jean; Université de Sherbrooke; Centre Hospitalier Universitaire de Sherbrooke","funders":"NIHR Exeter Clinical Research Facility; Eunice Kennedy Shriver National Institute of Child Health and Human Development; European Regional Development Fund; National Institute of Allergy and Infectious Diseases; Medical Research Council; Norges Forskningsråd; Novo Nordisk Fonden; Diabetesforbundet; Göteborgs Universitet; University of Bristol; National Institute for Health and Care Research; British Heart Foundation; Wellcome Trust; National Institutes of Health; Vetenskapsrådet; March of Dimes Foundation","keywords":"Biology; Fetus; Pleiotropy; Gestational age; Allele; Pregnancy; Gestation; Birth weight; Maternal effect; Genetics; Obstetrics; Gene; Medicine; Offspring; Phenotype","score_opus":0.026024670211944434,"score_gpt":0.3133095597693789,"score_spread":0.2872848895574345,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4362523789","genre_codex":"review","genre_gemma":"review","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"review","genre_consensus":"review","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.00019654396,0.9994573,0.00003377724,0.00013676602,0.00003737242,0.0000010479635,0.000018628161,0.0000015266636,0.00011696309],"genre_scores_gemma":[0.0016666576,0.998055,0.000058385936,0.00008006543,0.000055337132,0.0000029500684,0.000031836076,8.612866e-7,0.00004892155],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.99959034,0.0001472922,0.000073098105,0.000088547284,0.00007461992,0.000026186988],"domain_scores_gemma":[0.9978849,0.0016945493,0.0002060447,0.00003712398,0.00012700947,0.00005034696],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0012052153,0.0006949486,0.0020883796,0.0017540584,0.00013708301,0.0006406241,0.0008854445,0.00089378364,0.0018071737],"category_scores_gemma":[0.0032359587,0.0002645189,0.0012761434,0.0024407927,0.00043432545,0.0004509694,0.00048756588,0.00084625155,0.00035752254],"study_design_candidate":"not_applicable","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0006181795,0.000045023575,0.004764221,0.07605737,0.0039941436,0.00036281339,0.00009142267,0.0007581024,0.000637374,0.0025458003,0.011343548,0.89878196],"study_design_scores_gemma":[0.00033337437,0.00072692434,0.08281548,0.108100824,0.027649287,0.0082547115,0.00032943953,0.00090200943,0.0015546434,0.011050281,0.7581057,0.00017728256],"about_ca_topic_score_codex":0.0023716434,"about_ca_topic_score_gemma":0.0031083596,"teacher_disagreement_score":0.0023716434,"about_ca_system_score_codex":0.0006020138,"about_ca_system_score_gemma":0.0012054049,"threshold_uncertainty_score":0.0063738823},"labels":[],"label_agreement":null},{"id":"W4362661900","doi":"10.1038/s41588-023-01340-y","title":"Super-pangenome analyses highlight genomic diversity and structural variation across wild and cultivated tomato species","year":2023,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Plant Virus Research Studies","field":"Agricultural and Biological Sciences","cited_by":301,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Biotechnology Research Institute","funders":"Xinjiang Academy of Agricultural Sciences; University of California, Davis; Hebei University; National Key Research and Development Program of China; Chinese Academy of Agricultural Sciences; Institute of Crop Sciences, Chinese Academy of Agricultural Sciences; Anhui Agricultural University; National Natural Science Foundation of China; Chinese Academy of Tropical Agricultural Sciences; National Science Foundation","keywords":"Biology; Lycopersicon; Genome; Clade; Solanum; Genetic diversity; Genetics; Gene; Structural variation; Phylogenetics; Evolutionary biology; Botany; Biotechnology","score_opus":0.05344590146552544,"score_gpt":0.30466296469233717,"score_spread":0.2512170632268117,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4362661900","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9682119,0.00084675214,0.013125208,0.00012535711,0.000013693178,0.0000307117,0.014748169,0.00031021005,0.0025879731],"genre_scores_gemma":[0.9521677,0.00046531836,0.016828848,0.00014855614,0.000011959308,0.00005371959,0.029314075,0.00019809988,0.00081164454],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9998878,0.000010616452,0.0000063272873,0.00006368189,0.000016775197,0.000014722752],"domain_scores_gemma":[0.99973387,0.00008296561,0.000064153726,0.000043590157,0.000027615368,0.000047787435],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00018084452,0.0002173827,0.00025971603,0.0011879643,0.00023370248,0.00033504944,0.00018990798,0.00024453757,0.0024830278],"category_scores_gemma":[0.00039521503,0.00012280344,0.00036481294,0.0011541112,0.00018925236,0.0003921425,0.000536619,0.0004033035,0.00032515766],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0002671735,0.000026360854,0.019198162,0.00020953336,0.00014249458,0.00022191241,0.00031114178,0.0007137293,0.9646707,0.0006800597,0.00035138158,0.013207388],"study_design_scores_gemma":[0.000043895034,0.000268893,0.90168536,0.000064537584,0.00028663475,0.0013925715,0.00078340137,0.0055438755,0.06025403,0.0032774468,0.026346581,0.00005278517],"about_ca_topic_score_codex":0.000980556,"about_ca_topic_score_gemma":0.0029334996,"teacher_disagreement_score":0.0024830278,"about_ca_system_score_codex":0.0001906373,"about_ca_system_score_gemma":0.00011108811,"threshold_uncertainty_score":0.0083066225},"labels":[],"label_agreement":null},{"id":"W4362663646","doi":"10.1038/s41588-023-01366-2","title":"Precise modulation of transcription factor levels identifies features underlying dosage sensitivity","year":2023,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Genomics and Chromatin Dynamics","field":"Biochemistry, Genetics and Molecular Biology","cited_by":140,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Alberta Children's Hospital; University of Calgary","funders":"National Institute of General Medical Sciences; National Human Genome Research Institute; Vlaamse regering; NOMIS Stiftung; Stanford Research Computing Center, Stanford University; KU Leuven; National Institute of Dental and Craniofacial Research; Vlaams Supercomputer Centrum; Fonds Wetenschappelijk Onderzoek; Howard Hughes Medical Institute; Helen Hay Whitney Foundation; Damon Runyon Cancer Research Foundation; National Institutes of Health; U.S. Department of Health and Human Services","keywords":"Biology; Transcription factor; Computational biology; Sensitivity (control systems); Genetics; Gene","score_opus":0.022312796516398798,"score_gpt":0.2814509659095132,"score_spread":0.2591381693931144,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4362663646","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9851598,0.0011765634,0.011393344,0.00010772583,0.000014109762,0.000020280304,0.00044059125,0.00014978088,0.001537748],"genre_scores_gemma":[0.99758863,0.00021926496,0.0015490603,0.000034705234,0.000004753164,0.00001359101,0.00017919231,0.00003050023,0.00038031963],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.999647,0.00004412102,0.000033495886,0.00016245006,0.00008054241,0.00003239336],"domain_scores_gemma":[0.9996426,0.00011570383,0.00010010075,0.00008605228,0.000022132006,0.000033348388],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0002469238,0.00020588486,0.0002488182,0.00033197072,0.00010472828,0.00041674508,0.00020266593,0.00030983856,0.0012326363],"category_scores_gemma":[0.0005279092,0.00028119798,0.00018819662,0.00018815427,0.0004988836,0.00025332393,0.00032011265,0.0005098962,0.00031115854],"study_design_candidate":"bench_or_experimental","study_design_consensus":"bench_or_experimental","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.000027566077,0.0000029798518,0.00064588565,0.0000073324168,0.0000028529173,0.000008030735,0.00000844365,0.000074728756,0.99829787,0.00006608163,0.000005166804,0.0008530082],"study_design_scores_gemma":[0.0000050554613,0.00009722949,0.039984226,0.0000037348193,0.000013010425,0.00019878653,0.0000261981,0.0015234394,0.95718724,0.00025814195,0.0006937286,0.000009365215],"about_ca_topic_score_codex":0.00031251123,"about_ca_topic_score_gemma":0.00050892215,"teacher_disagreement_score":0.0012326363,"about_ca_system_score_codex":0.00030886295,"about_ca_system_score_gemma":0.000088804605,"threshold_uncertainty_score":0.004123509},"labels":[],"label_agreement":null},{"id":"W4375859145","doi":"10.1038/s41588-023-01384-0","title":"Genetic architecture of the inflammatory bowel diseases across East Asian and European ancestries","year":2023,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Inflammatory Bowel Disease","field":"Biochemistry, Genetics and Molecular Biology","cited_by":218,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Montreal Heart Institute; Mount Sinai Hospital; University of Manitoba","funders":"School of Life Sciences and Biotechnology Division of Life Sciences, Korea University; Japan Society for the Promotion of Science; University of Science and Technology of China; National Human Genome Research Institute; Genome Institute of Singapore; National Research Foundation of Korea; National Natural Science Foundation of China; National University of Singapore; National Research Foundation; Massachusetts General Hospital; Helsinki Institute of Life Science, Helsingin Yliopisto; National Center for Global Health and Medicine; National Institute of Diabetes and Digestive and Kidney Diseases; Stanley Center for Psychiatric Research, Broad Institute; Kela; Guangzhou Medical University; Broad Institute; Cedars-Sinai Medical Center; Japan Agency for Medical Research and Development; Tongji University; University of Ulsan; Helsingin Yliopisto","keywords":"Biology; Inflammatory bowel disease; Genetic architecture; Inflammatory Bowel Diseases; Genetics; Computational biology; Evolutionary biology; Disease; Gene; Phenotype; Medicine; Internal medicine","score_opus":0.004628428638804087,"score_gpt":0.23179557171866869,"score_spread":0.2271671430798646,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4375859145","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9974291,0.0007099057,0.00032027432,0.00012680092,0.0000073625333,0.0000044032886,0.00018098208,0.000007102892,0.0012139762],"genre_scores_gemma":[0.9986444,0.00044183058,0.00024534066,0.00004565499,0.000011880526,0.0000047424105,0.00015132914,0.000009968481,0.00044485636],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9988997,0.00039543974,0.00010885639,0.00031044325,0.000119682205,0.00016587222],"domain_scores_gemma":[0.9991461,0.00022645738,0.00028358432,0.00008938759,0.000111723515,0.00014270522],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0006340176,0.00050998805,0.00050323963,0.0020648814,0.000642586,0.00085829146,0.0004447086,0.0004902852,0.003427406],"category_scores_gemma":[0.001307657,0.00033389413,0.0006151194,0.0022308168,0.00073266955,0.00038451946,0.000987449,0.0004912414,0.00028166993],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.001931799,0.00012715899,0.9220882,0.00008250037,0.0010513201,0.002542543,0.0018295795,0.00049460493,0.05251276,0.0022178474,0.00032656442,0.014795142],"study_design_scores_gemma":[0.000013680971,0.000075771444,0.9964978,0.000019426583,0.00017104908,0.0011896479,0.0004699606,0.00018188573,0.0004757224,0.00051097583,0.00038361494,0.000010467189],"about_ca_topic_score_codex":0.0057668914,"about_ca_topic_score_gemma":0.0046361545,"teacher_disagreement_score":0.0057668914,"about_ca_system_score_codex":0.00031769773,"about_ca_system_score_gemma":0.0002967075,"threshold_uncertainty_score":0.011466682},"labels":[],"label_agreement":null},{"id":"W4376131713","doi":"10.1038/s41588-023-01412-z","title":"Author Correction: Genetic effects on the timing of parturition and links to fetal birth weight","year":2023,"lang":"en","type":"erratum","venue":"Nature Genetics","topic":"Preterm Birth and Chorioamnionitis","field":"Medicine","cited_by":1,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Centre Intégré Universitaire de Santé et de Services Sociaux du Saguenay–Lac-Saint-Jean; Université de Sherbrooke; Centre Hospitalier Universitaire de Sherbrooke","funders":"Eunice Kennedy Shriver National Institute of Child Health and Human Development; Medical Research Council; Wellcome Trust","keywords":"Biology; Section (typography); Genome-wide association study; Genetics; Birth weight; Pregnancy; Single-nucleotide polymorphism; Gene; Genotype; Computer science","score_opus":0.01199258326477843,"score_gpt":0.26823203658614403,"score_spread":0.2562394533213656,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4376131713","genre_codex":"editorial","genre_gemma":"other","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"other","genre_consensus":null,"domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.00020252669,0.00063663675,0.0016393309,0.023677219,0.968906,0.000021765365,0.0021227177,0.00042005145,0.002373739],"genre_scores_gemma":[0.030742949,0.008337293,0.02428449,0.0759799,0.34568715,0.00038880412,0.013755285,0.0065165395,0.49430764],"study_design_codex":"not_applicable","study_design_gemma":"not_applicable","domain_scores_codex":[0.99553514,0.000848494,0.0008118731,0.0008014999,0.0017247847,0.0002782223],"domain_scores_gemma":[0.9716116,0.008702266,0.0009972332,0.0018828327,0.015873114,0.0009328617],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0041172174,0.002987782,0.0020669843,0.0035679177,0.0025887955,0.0025930984,0.0035434763,0.0036112112,0.07444896],"category_scores_gemma":[0.066783704,0.0011327621,0.0017543763,0.0025273184,0.0012961995,0.0015683575,0.0018014584,0.008488534,0.031004546],"study_design_candidate":"not_applicable","study_design_consensus":"not_applicable","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.000039771687,0.000004606081,0.000108090244,0.00008726101,0.00001466351,0.00022699109,0.000028886325,0.000046615296,0.000051629395,0.00052226975,0.99450725,0.004361876],"study_design_scores_gemma":[0.00008359208,0.000022498245,0.0015145082,0.0005684334,0.00009961201,0.0020575067,0.000112202586,0.00051664084,0.00059243815,0.0027761722,0.9915945,0.00006187711],"about_ca_topic_score_codex":0.022430224,"about_ca_topic_score_gemma":0.029989162,"teacher_disagreement_score":0.07444896,"about_ca_system_score_codex":0.0028884986,"about_ca_system_score_gemma":0.0039191977,"threshold_uncertainty_score":0.24905658},"labels":[],"label_agreement":null},{"id":"W4376134699","doi":"10.1038/s41588-023-01390-2","title":"Mobile element variation contributes to population-specific genome diversification, gene regulation and disease risk","year":2023,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Wheat and Barley Genetics and Pathology","field":"Agricultural and Biological Sciences","cited_by":49,"is_retracted":false,"has_abstract":false,"route_ca_aff":false,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"","funders":"Common Fund; National Institute of Neurological Disorders and Stroke; National Cancer Institute; National Human Genome Research Institute; National Institute on Drug Abuse; National Institutes of Health; National Institute of Mental Health; National Heart, Lung, and Blood Institute; National Center for Geriatrics and Gerontology; Institute of Medical Science, University of Tokyo; NIH Office of the Director; Japan Society for the Promotion of Science; Ministry of Education, Culture, Sports, Science and Technology; University of Tokyo; Simons Foundation Autism Research Initiative; RIKEN; Japan Agency for Medical Research and Development; McGill University","keywords":"Biology; Genome-wide association study; Expression quantitative trait loci; Genetics; Quantitative trait locus; Enhancer; Genetic association; Genome; Computational biology; Population; Gene; Genotype; Gene expression; Single-nucleotide polymorphism","score_opus":0.010519456744141328,"score_gpt":0.2208849410047551,"score_spread":0.21036548426061374,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4376134699","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99820995,0.00014918171,0.0010483525,0.000033639546,0.0000038112541,0.000003974193,0.00006108279,0.00001528333,0.00047484922],"genre_scores_gemma":[0.99911684,0.000072674804,0.00033873672,0.000033164888,0.0000060434454,0.000003232754,0.00008402132,0.000011664664,0.00033363048],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9997793,0.0000399603,0.000013760401,0.00009572485,0.000029666196,0.00004166682],"domain_scores_gemma":[0.9996822,0.00013022727,0.000068434056,0.000035171408,0.000028089351,0.000055870867],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0003567269,0.00016493,0.00031295876,0.0008911687,0.00017799038,0.00053889037,0.0003261981,0.00054656214,0.0015278152],"category_scores_gemma":[0.00052025856,0.00020272682,0.00028574778,0.0004472519,0.00034070062,0.00023967406,0.000494764,0.0005922641,0.00024607984],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00026673157,0.00005107915,0.055883564,0.000032122658,0.00011660476,0.00018184412,0.00019025522,0.0004516461,0.9339349,0.0007829985,0.00007500055,0.00803322],"study_design_scores_gemma":[0.00004357501,0.00020625991,0.96735173,0.000011548596,0.00011213985,0.00094295206,0.0002987004,0.0036251443,0.024761023,0.0015077639,0.001106386,0.000032824144],"about_ca_topic_score_codex":0.00068753655,"about_ca_topic_score_gemma":0.0013906858,"teacher_disagreement_score":0.0015278152,"about_ca_system_score_codex":0.00021046665,"about_ca_system_score_gemma":0.00011139319,"threshold_uncertainty_score":0.0051110387},"labels":[],"label_agreement":null},{"id":"W4378211951","doi":"10.1038/s41588-023-01397-9","title":"Integrating genetics with single-cell multiomic measurements across disease states identifies mechanisms of beta cell dysfunction in type 2 diabetes","year":2023,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Pancreatic function and diabetes","field":"Medicine","cited_by":79,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Alberta","funders":"School of Medicine, University of California, San Diego; National Institute of Diabetes and Digestive and Kidney Diseases; National Institute of General Medical Sciences; University of California, San Diego; National Institutes of Health; U.S. Department of Health and Human Services","keywords":"Biology; Chromatin; Type 2 diabetes; Genetics; Beta cell; Gene; Transcriptome; Cell type; Phenotype; Computational biology; Gene expression; Islet; Cell; Diabetes mellitus; Endocrinology","score_opus":0.022285359087555533,"score_gpt":0.2661012155600512,"score_spread":0.24381585647249565,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4378211951","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9543941,0.0015798592,0.04082088,0.00050438376,0.00011384297,0.000022798795,0.0012505798,0.0003177665,0.0009957692],"genre_scores_gemma":[0.9822264,0.0009115953,0.01544891,0.00034831295,0.00004061893,0.000047351,0.00045796117,0.00010640186,0.00041251976],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.99975127,0.000043962227,0.000016962531,0.000093395676,0.00006174803,0.000032734322],"domain_scores_gemma":[0.9995141,0.0001606565,0.00014102155,0.00006762056,0.00004809745,0.00006837154],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0006255446,0.00043113352,0.00053927914,0.0006946913,0.00022352056,0.0012233328,0.00038032173,0.00062725024,0.0005750308],"category_scores_gemma":[0.0007879223,0.0003403964,0.0004491857,0.000468575,0.0005425838,0.0007084247,0.00095963624,0.001358843,0.00011986322],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00024604495,0.00004668242,0.023916101,0.00007342096,0.000115804745,0.000116369476,0.000099180375,0.0012295034,0.961647,0.00082249887,0.0002260742,0.0114614405],"study_design_scores_gemma":[0.00005522653,0.0005298014,0.45168447,0.00007082224,0.00043403334,0.0012568391,0.00055828254,0.030537399,0.50006586,0.010867316,0.0037972787,0.00014276897],"about_ca_topic_score_codex":0.0007327438,"about_ca_topic_score_gemma":0.0015564716,"teacher_disagreement_score":0.0012233328,"about_ca_system_score_codex":0.00044100927,"about_ca_system_score_gemma":0.00027923117,"threshold_uncertainty_score":0.0033082962},"labels":[],"label_agreement":null},{"id":"W4378715403","doi":"10.1038/s41588-023-01410-1","title":"Genome-wide association meta-analysis of spontaneous coronary artery dissection identifies risk variants and genes related to artery integrity and tissue-mediated coagulation","year":2023,"lang":"en","type":"review","venue":"Nature Genetics","topic":"Cardiovascular Issues in Pregnancy","field":"Medicine","cited_by":89,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Vancouver General Hospital; University of British Columbia","funders":"Common Fund; National Institute of Diabetes and Digestive and Kidney Diseases; National Cancer Institute; National Institute of Mental Health; National Heart, Lung, and Blood Institute; European Regional Development Fund; AstraZeneca; National Health and Medical Research Council; National Institutes of Health; U.S. Department of Defense; Société Française de Cardiologie; Medical Research Council; NSW Ministry of Health; Fédération Française de Cardiologie; Agence Nationale de la Recherche; National Institute of General Medical Sciences; Center for Individualized Medicine, Mayo Clinic; British Heart Foundation; National Institute for Health and Care Research; NIH Office of the Director; Cardiac Society of Australia and New Zealand; Michael Smith Health Research BC; Instituto de Salud Carlos III; Centre Hospitalier Universitaire de Clermont-Ferrand; FONDATION ALZHEIMER; A. Alfred Taubman Medical Research Institute; Victor Chang Cardiac Research Institute; University of Michigan; Canadian Institutes of Health Research; American Heart Association; Heart and Stroke Foundation of Canada","keywords":"Scad; Biology; Coronary artery disease; Genome-wide association study; Myocardial infarction; Genetic association; Bioinformatics; Gene; Genetics; Internal medicine; Single-nucleotide polymorphism; Medicine; Genotype","score_opus":0.035270384358171966,"score_gpt":0.3298470269949726,"score_spread":0.2945766426368006,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4378715403","genre_codex":"review","genre_gemma":"review","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"review","genre_consensus":"review","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.00039161803,0.9990152,0.00011947935,0.00020228869,0.000063768646,0.000003594854,0.000055774144,0.000006769115,0.00014159935],"genre_scores_gemma":[0.006517831,0.992428,0.0003372369,0.00027549698,0.00011756645,0.000011170085,0.00017126172,0.0000045092543,0.0001369515],"study_design_codex":"design_other","study_design_gemma":"meta_analysis","domain_scores_codex":[0.99936396,0.00022126165,0.00009484181,0.00013087271,0.00014086932,0.000048313585],"domain_scores_gemma":[0.9979961,0.0015009872,0.00020218642,0.00005316638,0.00018216806,0.00006553825],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.002117884,0.0011517599,0.004039368,0.0020757695,0.00017575445,0.00089991785,0.0009593391,0.0010417105,0.0023799196],"category_scores_gemma":[0.003335786,0.00034451325,0.0037706494,0.003056295,0.000269112,0.00041562828,0.0005877886,0.0012532867,0.00039908566],"study_design_candidate":"meta_analysis","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0016037116,0.00005958923,0.008011072,0.10857387,0.04821318,0.00057829364,0.00007476745,0.0011759055,0.0014662257,0.0015752666,0.020203503,0.8084645],"study_design_scores_gemma":[0.0013485732,0.0013825431,0.10194315,0.06903818,0.31577122,0.007347921,0.00026523674,0.0018697357,0.0029330219,0.009846598,0.48798633,0.0002675718],"about_ca_topic_score_codex":0.0021500252,"about_ca_topic_score_gemma":0.0048704143,"teacher_disagreement_score":0.004039368,"about_ca_system_score_codex":0.00065927935,"about_ca_system_score_gemma":0.0013749885,"threshold_uncertainty_score":0.011200607},"labels":[],"label_agreement":null},{"id":"W4379877956","doi":"10.1038/s41588-023-01408-9","title":"Genome-wide association study and functional characterization identifies candidate genes for insulin-stimulated glucose uptake","year":2023,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Genetic Associations and Epidemiology","field":"Biochemistry, Genetics and Molecular Biology","cited_by":74,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"McGill University","funders":"Steno Diabetes Center Aarhus; Common Fund; National Institute of Neurological Disorders and Stroke; Abbott Diagnostics; Bayer; National Cancer Institute; Quest Diagnostics; National Institute on Aging; Bayer Vital; National Institutes of Health; NIH Office of the Director; Novo Nordisk Fonden; Steno Diabetes Center Copenhagen; Danone; National Institute of General Medical Sciences; National Institute on Drug Abuse; Novo Nordisk; National Human Genome Research Institute; National Institute of Diabetes and Digestive and Kidney Diseases; Sanofi; National Center for Advancing Translational Sciences; Medical Research Council; AstraZeneca; National Institute of Mental Health; National Heart, Lung, and Blood Institute; Pfizer; Amgen","keywords":"Biology; Genome-wide association study; Candidate gene; Gene; Genetics; Genetic association; Insulin; Genome; Computational biology; Single-nucleotide polymorphism; Biotechnology; Genotype","score_opus":0.01192179507744932,"score_gpt":0.26537705512416354,"score_spread":0.2534552600467142,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4379877956","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99676406,0.00062333903,0.0015982357,0.00017025654,0.000022828806,0.000009843694,0.0003313171,0.000025167768,0.00045502672],"genre_scores_gemma":[0.9983399,0.00015843772,0.00082332396,0.0000415224,0.000019086601,0.000009270998,0.00027505538,0.000010552893,0.0003228383],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9990439,0.00043356934,0.00009601847,0.00022714862,0.00011960032,0.000079800564],"domain_scores_gemma":[0.9980369,0.00095526094,0.0004388908,0.0001991849,0.00015213381,0.00021757233],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0015617969,0.0006197356,0.00038398098,0.0018559421,0.00041498986,0.0007738686,0.00082949596,0.000859086,0.0015251406],"category_scores_gemma":[0.0021375085,0.0003892304,0.0009357638,0.001970164,0.00049412774,0.00027812904,0.00049827265,0.0009612733,0.00024823507],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.002962748,0.0002370628,0.95510405,0.000056975372,0.0012772921,0.0010798568,0.00015615964,0.00025347067,0.032085825,0.0004250024,0.00028091265,0.006080663],"study_design_scores_gemma":[0.000077806195,0.00018273048,0.9933702,0.000007858785,0.00045474264,0.0012611945,0.00011600134,0.0013915509,0.0024750833,0.00030346776,0.00034720628,0.0000121695775],"about_ca_topic_score_codex":0.002679683,"about_ca_topic_score_gemma":0.0018711677,"teacher_disagreement_score":0.002679683,"about_ca_system_score_codex":0.0002093277,"about_ca_system_score_gemma":0.00028733228,"threshold_uncertainty_score":0.008259654},"labels":[],"label_agreement":null},{"id":"W4380871380","doi":"10.1038/s41588-023-01419-6","title":"A complete telomere-to-telomere assembly of the maize genome","year":2023,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Chromosomal and Genetic Variations","field":"Agricultural and Biological Sciences","cited_by":315,"is_retracted":false,"has_abstract":true,"route_ca_aff":false,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"","funders":"National Key Research and Development Program of China; Institute of Genetics and Developmental Biology, Chinese Academy of Sciences; Chinese Academy of Sciences; Institute of Genetics; National Natural Science Foundation of China","keywords":"Biology; Genome; Telomere; Centromere; Transposable element; Contig; Genetics; Nanopore sequencing; Chromosome; Repeated sequence; Computational biology; DNA; Gene","score_opus":0.01967609318109395,"score_gpt":0.23841060500977984,"score_spread":0.2187345118286859,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4380871380","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.67250466,0.003685439,0.2329039,0.00039943456,0.00026796444,0.0005225218,0.07413438,0.00432862,0.011253087],"genre_scores_gemma":[0.5639761,0.00321302,0.27570403,0.00020227462,0.00006088191,0.0004772284,0.14232668,0.001800325,0.012239461],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99986804,0.000006690212,0.000007010821,0.00004719196,0.000049333285,0.000021712536],"domain_scores_gemma":[0.9998683,0.000012524786,0.000021844864,0.00002561871,0.00004714847,0.000024538178],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00014974485,0.000542807,0.0004916239,0.0007315668,0.00059427373,0.00054669316,0.00036243835,0.00034335253,0.0026597525],"category_scores_gemma":[0.00040410148,0.00040894927,0.0007867695,0.0010224598,0.0001534557,0.00031799715,0.00054400245,0.0006494002,0.001902486],"study_design_candidate":"bench_or_experimental","study_design_consensus":"bench_or_experimental","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00020662996,0.000015242108,0.0010011622,0.00022471262,0.000040804,0.00014863323,0.00012797551,0.0012759499,0.97746325,0.0008333337,0.001167662,0.017494697],"study_design_scores_gemma":[0.000102701386,0.00043386244,0.058221832,0.00013113365,0.00026994073,0.00079501135,0.00019439199,0.014408058,0.7775522,0.0023888438,0.1453595,0.00014255918],"about_ca_topic_score_codex":0.006300264,"about_ca_topic_score_gemma":0.0094408505,"teacher_disagreement_score":0.006300264,"about_ca_system_score_codex":0.00055513956,"about_ca_system_score_gemma":0.0010607318,"threshold_uncertainty_score":0.012527227},"labels":[],"label_agreement":null},{"id":"W4381185249","doi":"10.1038/s41588-023-01422-x","title":"Genome-wide association analyses define pathogenic signaling pathways and prioritize drug targets for IgA nephropathy","year":2023,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Renal Diseases and Glomerulopathies","field":"Medicine","cited_by":172,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Calgary; Toronto General Hospital; University of Toronto","funders":"National Human Genome Research Institute; National Institute of Allergy and Infectious Diseases; National Center for Advancing Translational Sciences; Medical Research Council; KfH-Stiftung Präventivmedizin; Gilead Sciences; Uniwersytet Medyczny im. Karola Marcinkowskiego w Poznaniu; Fresenius Medical Care North America; National Natural Science Foundation of China; Deutsche Forschungsgemeinschaft; U.S. National Library of Medicine; National Institute of Neurological Disorders and Stroke; Kidney Research UK; National Institute of General Medical Sciences; Bundesministerium für Bildung und Forschung; Albert-Ludwigs-Universität Freiburg; Medizinische Fakultät der Albert-Ludwigs-Universität Freiburg; Natera; National Institute of Arthritis and Musculoskeletal and Skin Diseases; National Institute of Diabetes and Digestive and Kidney Diseases; Všeobecná Fakultní Nemocnice v Praze; Amgen; Pirogov Russian National Research Medical University; U.S. Department of Veterans Affairs; U.S. Department of Health and Human Services; National Science Foundation","keywords":"Biology; Genome-wide association study; Computational biology; Nephropathy; Genetics; Genetic association; Genome; Drug discovery; Drug; Bioinformatics; Gene; Genotype; Single-nucleotide polymorphism; Pharmacology","score_opus":0.019243247861337142,"score_gpt":0.2908116887480404,"score_spread":0.2715684408867033,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4381185249","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.96713537,0.017414825,0.005911449,0.0030818644,0.00011817672,0.00004329584,0.0021542967,0.00022873834,0.0039120135],"genre_scores_gemma":[0.99242264,0.0031917663,0.002628126,0.00045489892,0.00008600027,0.000011286765,0.000757862,0.000031481046,0.00041587828],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9994948,0.00015121551,0.000051910883,0.000116354575,0.000101605176,0.00008398251],"domain_scores_gemma":[0.9989195,0.0005809957,0.0002817545,0.0000492972,0.00007132625,0.00009712792],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0011290681,0.0007929014,0.0008828276,0.0020616886,0.00042387893,0.0013699607,0.0005330284,0.0007369144,0.0030591004],"category_scores_gemma":[0.0018603747,0.00023808159,0.0013354154,0.001924767,0.00040379437,0.0003919248,0.00052540126,0.0009103076,0.0003303602],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0058601163,0.00041219566,0.7296467,0.0005637393,0.0062307003,0.0024051198,0.0001519292,0.004446242,0.10080119,0.002933718,0.004412047,0.14213626],"study_design_scores_gemma":[0.00064739404,0.0009904132,0.93116575,0.00019461368,0.0071769385,0.0035031952,0.00041712748,0.012431055,0.020921513,0.0076581095,0.014816793,0.00007706423],"about_ca_topic_score_codex":0.0015118826,"about_ca_topic_score_gemma":0.0038406334,"teacher_disagreement_score":0.0030591004,"about_ca_system_score_codex":0.0004131345,"about_ca_system_score_gemma":0.000750858,"threshold_uncertainty_score":0.0102337},"labels":[],"label_agreement":null},{"id":"W4381248768","doi":"10.1038/s41588-023-01429-4","title":"Transcriptomic classes of BCR-ABL1 lymphoblastic leukemia","year":2023,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Chronic Myeloid Leukemia Treatments","field":"Medicine","cited_by":56,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Hospital for Sick Children; Princess Margaret Cancer Centre; University of Toronto; Ontario Institute for Cancer Research","funders":"Canadian Institutes of Health Research; Hospital for Sick Children; Ontario Institute for Cancer Research; Princess Margaret Cancer Foundation; University Health Network; American Society of Hematology; V Foundation for Cancer Research","keywords":"Biology; Leukemia; Transcriptome; Cancer research; Tyrosine kinase; Progenitor cell; Stem cell; Immunology; Genetics; Signal transduction; Gene; Gene expression","score_opus":0.013382498910148753,"score_gpt":0.278462186968016,"score_spread":0.26507968805786725,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4381248768","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.97016114,0.002544059,0.0043839337,0.00021502133,0.000030447101,0.000054328895,0.0197153,0.00012655143,0.0027691927],"genre_scores_gemma":[0.97537476,0.001002166,0.0035910953,0.00019549554,0.000025873607,0.00012229879,0.016944993,0.00005583537,0.002687523],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.99983525,0.000014560442,0.00000936285,0.00006891342,0.000035743426,0.000036019435],"domain_scores_gemma":[0.99983215,0.000034612203,0.000061144616,0.000015852775,0.000031774758,0.000024384775],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00011435954,0.00016556118,0.000208578,0.00051297323,0.00018456727,0.00036308804,0.00010142081,0.00019082846,0.0015915388],"category_scores_gemma":[0.0003065013,0.00007474309,0.00017552721,0.0006666921,0.00017518878,0.00018632824,0.00026439206,0.00024536153,0.0003543367],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0004120251,0.000023169263,0.025887838,0.0001890646,0.00005127097,0.00014409842,0.00012370375,0.00024935402,0.9581293,0.0004609925,0.00057873985,0.013750448],"study_design_scores_gemma":[0.000041154934,0.00051471964,0.769662,0.000059524507,0.00021014402,0.0019618105,0.00061491056,0.0029276214,0.1945721,0.0023131268,0.027088689,0.00003414165],"about_ca_topic_score_codex":0.00046281068,"about_ca_topic_score_gemma":0.001048771,"teacher_disagreement_score":0.0015915388,"about_ca_system_score_codex":0.00023439848,"about_ca_system_score_gemma":0.00017900355,"threshold_uncertainty_score":0.005324185},"labels":[],"label_agreement":null},{"id":"W4382632577","doi":"10.1038/s41588-023-01428-5","title":"Large-scale multitrait genome-wide association analyses identify hundreds of glaucoma risk loci","year":2023,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Glaucoma and retinal disorders","field":"Medicine","cited_by":142,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Université de Montréal; Centre Hospitalier de l’Université de Montréal","funders":"National Eye Institute; National Health and Medical Research Council; Medical Research Council; Menzies Institute for Medical Research; Flinders University; Moorfields Eye Hospital NHS Foundation Trust; Université de Montréal; Lister Institute of Preventive Medicine; University of Tasmania; Canadian Institutes of Health Research; QIMR Berghofer Medical Research Institute; Duke-NUS Medical School; RIKEN; National Institutes of Health; School of Medicine, Case Western Reserve University; University of Wisconsin-Madison; National Institute for Health and Care Research; Case Western Reserve University; Massachusetts General Hospital; Research to Prevent Blindness; Glaucoma Research Foundation; BrightFocus Foundation; Government of Canada; U.S. Department of Health and Human Services","keywords":"Genome-wide association study; Glaucoma; Biology; Genetic association; Missing heritability problem; Heritability; Genetics; Open angle glaucoma; Intraocular pressure; Single-nucleotide polymorphism; Medicine; Ophthalmology; Genotype; Gene","score_opus":0.012740798489844196,"score_gpt":0.3141889231512906,"score_spread":0.3014481246614464,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4382632577","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9451695,0.0022564079,0.044145875,0.0010906828,0.00010597879,0.00011416303,0.0047489675,0.00047198043,0.0018963992],"genre_scores_gemma":[0.9739633,0.0005437936,0.021742128,0.00036100362,0.00006394879,0.00010419892,0.0024220406,0.00009054357,0.00070889597],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9972459,0.001077796,0.00016300786,0.0009541993,0.0003700563,0.00018900013],"domain_scores_gemma":[0.99502593,0.0027911311,0.0006399753,0.0010447365,0.00022979535,0.0002685043],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0037632445,0.0007027294,0.0009647999,0.0014974289,0.0010451912,0.0010942629,0.00069956743,0.00074117247,0.0035968344],"category_scores_gemma":[0.006071868,0.00039233643,0.0016584788,0.0019448373,0.0005141572,0.0004454553,0.0014608254,0.0012142973,0.00041866396],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.002351297,0.0005344971,0.77084386,0.00041116722,0.009321625,0.001950521,0.00086748874,0.006964916,0.09884769,0.0029749738,0.0040975334,0.10083448],"study_design_scores_gemma":[0.00034417992,0.00029568336,0.9687742,0.000058117876,0.0022244158,0.0011892272,0.0001591937,0.010566544,0.006325329,0.004293085,0.0056962073,0.00007397901],"about_ca_topic_score_codex":0.0040500388,"about_ca_topic_score_gemma":0.012424709,"teacher_disagreement_score":0.0040500388,"about_ca_system_score_codex":0.00032942486,"about_ca_system_score_gemma":0.00044404925,"threshold_uncertainty_score":0.01990217},"labels":[],"label_agreement":null},{"id":"W4385628976","doi":"10.1038/s41588-023-01469-w","title":"PhenoScore quantifies phenotypic variation for rare genetic diseases by combining facial analysis with other clinical features using a machine-learning framework","year":2023,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Genomics and Rare Diseases","field":"Biochemistry, Genetics and Molecular Biology","cited_by":74,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Université de Montréal","funders":"National Institute of General Medical Sciences; Medical Research Council; National Institutes of Health; National Health and Medical Research Council; European Commission; National Institute for Health and Care Research; Universiteit Antwerpen; Office for People With Developmental Disabilities","keywords":"Phenotype; Phenomics; Biology; Computational biology; Genetics; Phenotypic trait; Variation (astronomy); Genotype-phenotype distinction; Gene; Genomics; Genome","score_opus":0.01451055269996052,"score_gpt":0.31049372179268986,"score_spread":0.2959831690927293,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4385628976","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.7156295,0.00056554907,0.27091077,0.00036708234,0.0000853932,0.00016749691,0.0045532878,0.0023833043,0.005337607],"genre_scores_gemma":[0.91037524,0.00014955152,0.08621994,0.00015010149,0.00005887832,0.00008228303,0.0015456111,0.00019211606,0.0012262095],"study_design_codex":"observational","study_design_gemma":"simulation_or_modeling","domain_scores_codex":[0.9994823,0.00010351502,0.00003815841,0.00016845933,0.00015004475,0.000057597703],"domain_scores_gemma":[0.99867475,0.00058844814,0.00032354402,0.000118257165,0.00020866496,0.00008631919],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0009926755,0.00091965264,0.0007525994,0.0025690226,0.00023377602,0.0007043046,0.0005118952,0.0005205148,0.0019430122],"category_scores_gemma":[0.002500318,0.00020721975,0.0006965426,0.000924025,0.00034490039,0.0005134262,0.001003156,0.00050962897,0.00038705618],"study_design_candidate":"simulation_or_modeling","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00092571066,0.0003668175,0.53381896,0.00019085292,0.0007194997,0.0007692121,0.000087136425,0.030553073,0.13314667,0.0031846368,0.004709536,0.29152787],"study_design_scores_gemma":[0.00007127212,0.00034810885,0.46006468,0.000045906545,0.00031635186,0.0026356634,0.00010970552,0.48279947,0.0412201,0.00925351,0.0030347914,0.00010039762],"about_ca_topic_score_codex":0.0026846065,"about_ca_topic_score_gemma":0.006053051,"teacher_disagreement_score":0.0026846065,"about_ca_system_score_codex":0.00038192037,"about_ca_system_score_gemma":0.00038593865,"threshold_uncertainty_score":0.0065000653},"labels":[],"label_agreement":null},{"id":"W4385708758","doi":"10.1038/s41588-023-01444-5","title":"Converging evidence from exome sequencing and common variants implicates target genes for osteoporosis","year":2023,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Bone Metabolism and Diseases","field":"Biochemistry, Genetics and Molecular Biology","cited_by":27,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"McGill Genome Centre; McGill University Health Centre; McGill University; Jewish General Hospital","funders":"Medical Research Council; Fonds de Recherche du Québec - Santé; National Institutes of Health; National Institute for Health and Care Research; Jewish General Hospital; Public Health Agency; European Commission; King's College London; Fondation de l'Hôpital général juif; Novo Nordisk Fonden; Canadian Institutes of Health Research; Compute Canada; McGill University; Public Health Agency of Canada; Wellcome Trust","keywords":"Biology; Exome sequencing; Genetics; Exome; Gene; Computational biology; Bioinformatics; Phenotype","score_opus":0.01875426537522439,"score_gpt":0.285597685514024,"score_spread":0.2668434201387996,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4385708758","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.93275446,0.026862562,0.014641435,0.006987839,0.0006129304,0.000041935215,0.007223346,0.000261539,0.01061388],"genre_scores_gemma":[0.97317964,0.011415906,0.007226113,0.0021536443,0.0004739694,0.000030982206,0.0034537106,0.00010009137,0.0019658024],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9989561,0.00010323896,0.000117598385,0.00042693614,0.00027820398,0.00011787618],"domain_scores_gemma":[0.9962985,0.0021999734,0.0004983787,0.0003623469,0.00036917307,0.00027172614],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0013931672,0.00108892,0.001115917,0.003044264,0.00057545194,0.001665936,0.00095916644,0.0022922286,0.007486938],"category_scores_gemma":[0.004245623,0.0004849935,0.0014050383,0.002085082,0.0011011878,0.0010098115,0.001446381,0.0014806534,0.0007152941],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0047442913,0.00024097944,0.5998311,0.0012412765,0.006320102,0.019504098,0.0008853061,0.002037973,0.2478313,0.010487695,0.004598884,0.102277],"study_design_scores_gemma":[0.0003605282,0.00039584763,0.8905049,0.00055253005,0.004058562,0.024303637,0.0007852103,0.0025788199,0.028484464,0.024465872,0.023385968,0.00012369071],"about_ca_topic_score_codex":0.0018295358,"about_ca_topic_score_gemma":0.0029487018,"teacher_disagreement_score":0.007486938,"about_ca_system_score_codex":0.00028190395,"about_ca_system_score_gemma":0.00038889013,"threshold_uncertainty_score":0.025046289},"labels":[],"label_agreement":null},{"id":"W4385948292","doi":"10.1038/s41588-023-01466-z","title":"Exome sequencing identifies breast cancer susceptibility genes and defines the contribution of coding variants to breast cancer risk","year":2023,"lang":"en","type":"review","venue":"Nature Genetics","topic":"BRCA gene mutations in cancer","field":"Biochemistry, Genetics and Molecular Biology","cited_by":63,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Université Laval; Centre hospitalier de l'Université Laval; Centre hospitalier universitaire de Québec","funders":"National Cancer Institute; Servicio Gallego de Salud; Medical Research Council; Canadian Institutes of Health Research; Horizon 2020 Framework Programme; National Institutes of Health; Freistaat Sachsen; Agence Nationale de Sécurité Sanitaire de l’Alimentation, de l’Environnement et du Travail; Institut National Du Cancer; Deutsche Krebshilfe; Ministerio de Economía y Competitividad; National University Health System; Fondation de France; University of Manchester; Instituto de Salud Carlos III; Xunta de Galicia; National University of Singapore; Wellcome Trust; Cancer Research UK; University College London; National Medical Research Council; Research Promotion Foundation; University of Cambridge; Deutsche Forschungsgemeinschaft; Wellcome; NIHR Biomedical Research Centre, Royal Marsden NHS Foundation Trust/Institute of Cancer Research; Government of Canada; Fondation du cancer du sein du Québec; European Regional Development Fund; Bundesministerium für Bildung und Forschung; National Institute for Health and Care Research; Genome Canada; Deutsches Krebsforschungszentrum; European Commission; Knight Cancer Institute, Oregon Health and Science University; Oregon Health and Science University; Agence Nationale de la Recherche","keywords":"CHEK2; PALB2; Biology; Breast cancer; Exome sequencing; Exome; Missense mutation; Genetics; CDKN2A; Gene; Cancer; Mutation; Germline mutation","score_opus":0.025393833297672835,"score_gpt":0.3411986819226214,"score_spread":0.3158048486249486,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4385948292","genre_codex":"review","genre_gemma":"review","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"review","genre_consensus":"review","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.00015954585,0.99875355,0.00021061176,0.00031289828,0.00009605961,0.0000030902793,0.000052972162,0.0000059422687,0.00040527797],"genre_scores_gemma":[0.0011250572,0.9979102,0.00023207479,0.00022940758,0.00009720567,0.0000075927883,0.00009312835,0.0000027782708,0.00030244654],"study_design_codex":"design_other","study_design_gemma":"systematic_review","domain_scores_codex":[0.9996835,0.000088160596,0.000041258256,0.00007593565,0.00008521389,0.00002598629],"domain_scores_gemma":[0.99918526,0.0005375543,0.000076808865,0.000023254479,0.00014051852,0.000036550082],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0012197061,0.00080859696,0.0019490599,0.0020716684,0.00012048949,0.00077029865,0.00082447234,0.00091780914,0.0023943856],"category_scores_gemma":[0.0015322703,0.00031050981,0.0007297414,0.0020132267,0.00036089888,0.0005854551,0.0005942941,0.001355738,0.001167579],"study_design_candidate":"systematic_review","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00017369099,0.000022921624,0.0007988033,0.01501136,0.00060532195,0.00019260653,0.000023973345,0.00039725367,0.0013409326,0.002450868,0.018811002,0.9601712],"study_design_scores_gemma":[0.00010127667,0.00021070021,0.011108443,0.0131349685,0.0016576776,0.0034391915,0.00008068915,0.0004101921,0.0015863511,0.0058383285,0.9623754,0.000056739056],"about_ca_topic_score_codex":0.0011919847,"about_ca_topic_score_gemma":0.0018040282,"teacher_disagreement_score":0.0023943856,"about_ca_system_score_codex":0.00061661616,"about_ca_system_score_gemma":0.0008592964,"threshold_uncertainty_score":0.00800997},"labels":[],"label_agreement":null},{"id":"W4385955298","doi":"10.1038/s41588-023-01475-y","title":"Genetic insights into human cortical organization and development through genome-wide analyses of 2,347 neuroimaging phenotypes","year":2023,"lang":"en","type":"review","venue":"Nature Genetics","topic":"Genetic Associations and Epidemiology","field":"Biochemistry, Genetics and Molecular Biology","cited_by":79,"is_retracted":false,"has_abstract":true,"route_ca_aff":false,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"","funders":"National Institute of Mental Health; Medical Research Council; Junta de Andalucía; British Academy; McGill University; Department of Health and Social Care; National Institute for Health and Care Research; Canada First Research Excellence Fund; Simons Foundation Autism Research Initiative; National Institute on Drug Abuse; UK Research and Innovation; NIHR Cambridge Biomedical Research Centre; Wellcome Trust","keywords":"Biology; Phenotype; Genetic architecture; Genome-wide association study; Neuroimaging; Neuroscience; Brain size; Cerebral cortex; Evolutionary biology; Genome; Functional magnetic resonance imaging; Gene; Gene regulatory network; Diffusion MRI; Genetics; Magnetic resonance imaging; Gene expression; Single-nucleotide polymorphism; Genotype","score_opus":0.04824202135510387,"score_gpt":0.361907527070559,"score_spread":0.31366550571545515,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4385955298","genre_codex":"review","genre_gemma":"review","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"review","genre_consensus":"review","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.0002561902,0.9988096,0.00026284723,0.00030779405,0.000038830913,0.00000266512,0.000060638653,0.0000067953883,0.00025478384],"genre_scores_gemma":[0.002024845,0.9971501,0.00035465223,0.00016824457,0.000080954145,0.00000649188,0.00010873933,0.0000024481355,0.00010350737],"study_design_codex":"design_other","study_design_gemma":"observational","domain_scores_codex":[0.999493,0.0001561496,0.00007303149,0.00014899814,0.000101341684,0.000027417853],"domain_scores_gemma":[0.99815625,0.0013233954,0.00016976274,0.000058128167,0.00022701043,0.000065373206],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0020415597,0.0011772005,0.002194218,0.0036738894,0.00014917436,0.0009438166,0.0009559668,0.0009900791,0.0014948993],"category_scores_gemma":[0.0028414002,0.00042941718,0.0011946168,0.0037909464,0.0007013074,0.00081500056,0.000737824,0.0013785489,0.0006389502],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00027160303,0.000028713423,0.0051836553,0.021017762,0.0026618787,0.00044572446,0.000060424853,0.00086987595,0.0015237671,0.0035390356,0.012858565,0.951539],"study_design_scores_gemma":[0.00023812384,0.0005236474,0.08944767,0.026778096,0.014421746,0.009894151,0.00026497355,0.0010822985,0.0032086489,0.019991271,0.8339355,0.00021387238],"about_ca_topic_score_codex":0.0032074447,"about_ca_topic_score_gemma":0.004678382,"teacher_disagreement_score":0.0036738894,"about_ca_system_score_codex":0.0007824058,"about_ca_system_score_gemma":0.0018085007,"threshold_uncertainty_score":0.010796964},"labels":[],"label_agreement":null},{"id":"W4386332807","doi":"10.1038/s41588-023-01485-w","title":"GWAS meta-analysis of over 29,000 people with epilepsy identifies 26 risk loci and subtype-specific genetic architecture","year":2023,"lang":"en","type":"review","venue":"Nature Genetics","topic":"Genetics and Neurodevelopmental Disorders","field":"Biochemistry, Genetics and Molecular Biology","cited_by":212,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Alberta Children's Hospital; University of Calgary; Université de Montréal; University Health Network; University of Toronto","funders":"Eunice Kennedy Shriver National Institute of Child Health and Human Development; National Institute of Neurological Disorders and Stroke; National Institute of Mental Health; National Heart, Lung, and Blood Institute; European Regional Development Fund; Janssen Biotech; Medical Research Council; Stanley Center for Psychiatric Research, Broad Institute; Genentech; National Institutes of Health; National Human Genome Research Institute; Epilepsy Society; Business Finland; Academy of Finland; Broad Institute; Fonds National de la Recherche Luxembourg; National Health and Medical Research Council; AstraZeneca; Fundação de Amparo à Pesquisa do Estado de São Paulo; Celgene; Novartis; University of Melbourne; Wellcome Trust; University College London; Maze Therapeutics; European Commission; National Institute of Child Health and Human Development; National Institute of Diabetes and Digestive and Kidney Diseases; Sanofi; Pfizer; Biogen; National Institute for Health and Care Research; UK Research and Innovation; Science Foundation Ireland; Massachusetts General Hospital; Deutsche Forschungsgemeinschaft; GlaxoSmithKline; Bristol-Myers Squibb; Australian Government; Cooley's Anemia Foundation","keywords":"Genetic architecture; Genome-wide association study; Biology; Epilepsy; Genetics; Heritability; Genetic association; SNP; Gene; Missing heritability problem; Quantitative trait locus; Computational biology; Genetic variants; Single-nucleotide polymorphism; Neuroscience; Genotype","score_opus":0.0242797634898504,"score_gpt":0.28358543559284227,"score_spread":0.2593056721029919,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4386332807","genre_codex":"review","genre_gemma":"review","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"review","genre_consensus":"review","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.00045953313,0.9982863,0.0003030749,0.00030664803,0.00008265978,0.000007272226,0.00016352347,0.000015302643,0.00037575388],"genre_scores_gemma":[0.0065505453,0.99174726,0.00055086444,0.00030554456,0.00012763451,0.000017873106,0.0003998119,0.000007222655,0.00029318043],"study_design_codex":"design_other","study_design_gemma":"meta_analysis","domain_scores_codex":[0.99948335,0.00016554078,0.00008282048,0.000109510554,0.000117703334,0.00004104649],"domain_scores_gemma":[0.9987596,0.0008738423,0.000127664,0.000043376538,0.00013995684,0.00005549092],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0019760514,0.001386159,0.0041294536,0.0021613417,0.0001752581,0.00095033424,0.0010486565,0.0008496969,0.003488982],"category_scores_gemma":[0.0022675162,0.00036360204,0.003416308,0.0032692729,0.00025046934,0.00046230623,0.0006507948,0.0011288535,0.00071481033],"study_design_candidate":"meta_analysis","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0013085265,0.000046468824,0.007057494,0.068661466,0.03591293,0.0005813416,0.00005115828,0.0012525518,0.0010733934,0.0022125717,0.022740684,0.8591014],"study_design_scores_gemma":[0.0010411321,0.0008852497,0.064678766,0.043906204,0.18825905,0.0066664303,0.00018564594,0.0014449981,0.0024546268,0.0107476115,0.67951405,0.00021617017],"about_ca_topic_score_codex":0.0025435307,"about_ca_topic_score_gemma":0.0066857478,"teacher_disagreement_score":0.0041294536,"about_ca_system_score_codex":0.0006726736,"about_ca_system_score_gemma":0.0015325937,"threshold_uncertainty_score":0.011671841},"labels":[],"label_agreement":null},{"id":"W4386516282","doi":"10.1038/s41588-023-01462-3","title":"GWAS of random glucose in 476,326 individuals provide insights into diabetes pathophysiology, complications and treatment stratification","year":2023,"lang":"en","type":"review","venue":"Nature Genetics","topic":"Diabetes Management and Research","field":"Medicine","cited_by":102,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"McGill University","funders":"Helmholtz Zentrum München; Lee Kong Chian School of Medicine, Nanyang Technological University; CARIM School for Cardiovascular Diseases, Universiteit Maastricht; Barts and The London School of Medicine and Dentistry; National Health and Medical Research Council; National Institute of Diabetes and Digestive and Kidney Diseases; World Cancer Research Fund; University of Ioannina; UK Dementia Research Institute; H. Lundbeck A/S; Novo Nordisk Foundation Center for Basic Metabolic Research; Medical Research Council; Tartu Ülikool; Uppsala Universitet; Russian Science Foundation; Lomonosov Moscow State University; Ludwig-Maximilians-Universität München; Centre National de la Recherche Scientifique; Université de Lille; King Abdulaziz University; University of Queensland; Karolinska Institutet; Universiteit Maastricht; KU Leuven; Horizon 2020 Framework Programme; Vetenskapsrådet; Deutsches Zentrum für Herz-Kreislaufforschung; Università degli Studi di Trento; Novo Nordisk; Agence Nationale de la Recherche; Hjärt-Lungfonden; Lundbeckfonden; University of South Australia; European Foundation for the Study of Diabetes; University of Glasgow; World Cancer Research Fund International; Erasmus Medisch Centrum; School of Public Health, Imperial College London; University of Oxford; Biotechnology and Biological Sciences Research Council; Nanyang Technological University; Universität Ulm; Society for Endocrinology; British Heart Foundation; Barts Charity; Massachusetts General Hospital; UK Research and Innovation; Lunds Universitet; Vanderbilt Institute for Clinical and Translational Research; European Genomic Institute for Diabetes; Universitetet i Tromsø; Imperial College London; Novo Nordisk Fonden; Università degli Studi di Ferrara; South Australian Health and Medical Research Institute; Norges Teknisk-Naturvitenskapelige Universitet; Alzheimer's Society; Diabetes UK; Research England; Engineering and Physical Sciences Research Council; European Commission; Helsingin Yliopisto; Technische Universität München; University of Exeter; University of Surrey; Amgen; Royal Society; University of North Carolina at Chapel Hill; Science for Life Laboratory; Queen Mary University of London; Vlaamse regering; National Institute for Health and Care Research; Mindich Child Health and Development Institute, Icahn School of Medicine at Mount Sinai; Coventry University; Wellcome Trust; Vanderbilt University","keywords":"Biology; Genome-wide association study; Pathophysiology; Diabetes mellitus; Risk stratification; Computational biology; Stratification (seeds); Bioinformatics; Internal medicine; Endocrinology; Genetics; Medicine; Single-nucleotide polymorphism; Gene; Genotype","score_opus":0.04786816812498351,"score_gpt":0.3710914116177779,"score_spread":0.3232232434927944,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4386516282","genre_codex":"review","genre_gemma":"review","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"review","genre_consensus":"review","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.00028567234,0.99745554,0.0004149201,0.00047088423,0.00020570046,0.000008961683,0.0001645952,0.00001668488,0.0009771335],"genre_scores_gemma":[0.0022134301,0.9954972,0.00067917915,0.0004674218,0.00021042017,0.000014997828,0.00030343473,0.0000060059574,0.0006079426],"study_design_codex":"design_other","study_design_gemma":"observational","domain_scores_codex":[0.99961036,0.00011084997,0.00006893414,0.00007711258,0.00010397761,0.00002874685],"domain_scores_gemma":[0.9989724,0.0006580302,0.00011047158,0.000039895014,0.00015966728,0.00005945371],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0015753148,0.0011553796,0.0023146954,0.002502575,0.0001600776,0.0008064082,0.00073686906,0.00093015516,0.003669366],"category_scores_gemma":[0.0019676501,0.0002944424,0.001053901,0.0025282598,0.00034900277,0.00069345837,0.0005602094,0.0011504425,0.0019566212],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00024354561,0.000030047739,0.0010014022,0.014846882,0.00093666196,0.00017367318,0.000031500153,0.000290249,0.0010075824,0.002383365,0.019265361,0.9597898],"study_design_scores_gemma":[0.0001029507,0.00019380731,0.008489493,0.008748097,0.0021800722,0.0016879751,0.00006081841,0.00021424073,0.000850011,0.0037162274,0.97370696,0.00004945143],"about_ca_topic_score_codex":0.0013395636,"about_ca_topic_score_gemma":0.0024979666,"teacher_disagreement_score":0.003669366,"about_ca_system_score_codex":0.0006582412,"about_ca_system_score_gemma":0.0011711495,"threshold_uncertainty_score":0.012275219},"labels":[],"label_agreement":null},{"id":"W4387019201","doi":"10.1038/s41588-023-01531-7","title":"Author Correction: Multi-ancestry genome-wide association analyses improve resolution of genes and pathways influencing lung function and chronic obstructive pulmonary disease risk","year":2023,"lang":"en","type":"erratum","venue":"Nature Genetics","topic":"Chronic Obstructive Pulmonary Disease (COPD) Research","field":"Medicine","cited_by":2,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"McGill University","funders":"National Cancer Institute; Biotechnology and Biological Sciences Research Council; National Heart, Lung, and Blood Institute; Medical Research Council; National Institute for Health and Care Research; Wellcome Trust","keywords":"Biology; Genome-wide association study; Lung function; Disease; Gene; Genetics; Pulmonary disease; Genome; Computational biology; Function (biology); Genetic association; Bioinformatics; Lung; Single-nucleotide polymorphism; Internal medicine; Genotype; Medicine","score_opus":0.024081132116499742,"score_gpt":0.314244956539835,"score_spread":0.2901638244233352,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4387019201","genre_codex":"editorial","genre_gemma":"other","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"other","genre_consensus":null,"domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.00046135316,0.00078218384,0.005225705,0.035269994,0.94588816,0.00006729506,0.0069440906,0.0015528273,0.0038083822],"genre_scores_gemma":[0.06118998,0.007635008,0.05947733,0.102822304,0.268153,0.0011844683,0.030335397,0.020813616,0.44838896],"study_design_codex":"not_applicable","study_design_gemma":"not_applicable","domain_scores_codex":[0.9878492,0.002441882,0.0024134123,0.0021530534,0.004378607,0.00076385704],"domain_scores_gemma":[0.9273659,0.024133114,0.0032961213,0.0064859525,0.036860842,0.001858083],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0095647955,0.0029713237,0.0026039989,0.0043064463,0.0037205776,0.004464212,0.0043043755,0.0048923907,0.15506104],"category_scores_gemma":[0.14103796,0.0017032737,0.0025215908,0.004066386,0.002172973,0.0023971186,0.003396819,0.010759741,0.062077064],"study_design_candidate":"not_applicable","study_design_consensus":"not_applicable","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00007833465,0.000006756711,0.00020361175,0.00022065938,0.000035293077,0.00031739607,0.00005624198,0.00005826441,0.00010885349,0.00089360704,0.99144965,0.0065712677],"study_design_scores_gemma":[0.00017523397,0.000029835022,0.0017633892,0.0009208415,0.00018349866,0.0020693848,0.0001591812,0.0008138121,0.0011607952,0.0056480323,0.98697346,0.000102473474],"about_ca_topic_score_codex":0.0116863875,"about_ca_topic_score_gemma":0.015339701,"teacher_disagreement_score":0.15506104,"about_ca_system_score_codex":0.0032872239,"about_ca_system_score_gemma":0.005842996,"threshold_uncertainty_score":0.5187309},"labels":[],"label_agreement":null},{"id":"W4387051937","doi":"10.1038/s41588-023-01549-x","title":"Author Correction: Exome sequencing identifies breast cancer susceptibility genes and defines the contribution of coding variants to breast cancer risk","year":2023,"lang":"en","type":"erratum","venue":"Nature Genetics","topic":"Nutrition, Genetics, and Disease","field":"Biochemistry, Genetics and Molecular Biology","cited_by":0,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Université Laval; Centre hospitalier de l'Université Laval; Centre hospitalier universitaire de Québec","funders":"","keywords":"Biology; Breast cancer; Exome sequencing; Exome; Genetics; Gene; Computational biology; Cancer; Bioinformatics; Mutation","score_opus":0.011114682033811961,"score_gpt":0.28464709829612556,"score_spread":0.2735324162623136,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4387051937","genre_codex":"editorial","genre_gemma":"other","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"other","genre_consensus":null,"domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.00034406333,0.0006685996,0.002160928,0.0904137,0.9000704,0.000029135465,0.0022113016,0.00065932143,0.0034424388],"genre_scores_gemma":[0.02961342,0.007858478,0.022599742,0.22652327,0.29366624,0.00029212612,0.0080475975,0.005076735,0.40632248],"study_design_codex":"not_applicable","study_design_gemma":"not_applicable","domain_scores_codex":[0.99568284,0.000703222,0.00077326986,0.00068699016,0.0018801885,0.00027343634],"domain_scores_gemma":[0.9725822,0.008538638,0.0012330667,0.0013394326,0.015248336,0.0010584325],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.004615194,0.002156215,0.0014744604,0.0026044238,0.002813057,0.0031374712,0.0028371047,0.0060872943,0.040533543],"category_scores_gemma":[0.059150938,0.000985126,0.0013281677,0.001723929,0.0019255943,0.0016078333,0.0015590184,0.011947839,0.024002796],"study_design_candidate":"not_applicable","study_design_consensus":"not_applicable","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.000034470402,0.000005759143,0.00010420046,0.000065898836,0.000013702515,0.0006224171,0.00003845415,0.000043157837,0.000094171475,0.00066690805,0.99464357,0.0036672459],"study_design_scores_gemma":[0.00007538014,0.000018575638,0.00084338867,0.0003882869,0.000084968655,0.0035138465,0.000108886634,0.00044684837,0.0009270373,0.00262751,0.9909054,0.000059891623],"about_ca_topic_score_codex":0.021752343,"about_ca_topic_score_gemma":0.027621543,"teacher_disagreement_score":0.040533543,"about_ca_system_score_codex":0.0029784574,"about_ca_system_score_gemma":0.00474572,"threshold_uncertainty_score":0.13559818},"labels":[],"label_agreement":null},{"id":"W4387363979","doi":"10.1038/s41588-023-01520-w","title":"Genome-wide association study of placental weight identifies distinct and shared genetic influences between placental and fetal growth","year":2023,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Birth, Development, and Health","field":"Medicine","cited_by":66,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Centre Intégré Universitaire de Santé et de Services Sociaux du Saguenay–Lac-Saint-Jean; Centre Hospitalier Universitaire de Sherbrooke; Université de Sherbrooke; McGill University","funders":"Eunice Kennedy Shriver National Institute of Child Health and Human Development; National Institute of Environmental Health Sciences; Medical Research Council; Novo Nordisk Fonden; Lundbeckfonden; Wellcome Trust","keywords":"Biology; Placenta; Genome-wide association study; Genetics; Fetal growth; Genetic association; Fetus; Single-nucleotide polymorphism; Pregnancy; Genotype; Gene","score_opus":0.013670721992963028,"score_gpt":0.2821435191281246,"score_spread":0.26847279713516153,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4387363979","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99801683,0.00055092043,0.00082332216,0.000039892366,0.0000037070877,0.000002867808,0.00016378268,0.000013666785,0.00038503672],"genre_scores_gemma":[0.9989513,0.00019661259,0.0005378404,0.00001131001,0.0000052161154,0.0000035475284,0.00015465861,0.00000605469,0.00013342442],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9994276,0.00020063155,0.000031523687,0.00017930892,0.000097528085,0.0000632576],"domain_scores_gemma":[0.9986809,0.0005712645,0.000426867,0.00014828338,0.000055993456,0.00011664185],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00066729385,0.00032198985,0.0002663877,0.0013215138,0.00027147902,0.0003913924,0.00024808766,0.00026053074,0.0016291087],"category_scores_gemma":[0.001967475,0.00019724236,0.00030605774,0.0013974506,0.00049528637,0.0001351182,0.0005468297,0.00042728303,0.00011205723],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0008550909,0.000039614242,0.94437706,0.00005182695,0.0007613921,0.0005112932,0.00021117211,0.00018907695,0.040406413,0.00030525937,0.00013951476,0.012152319],"study_design_scores_gemma":[0.000011500934,0.00004299797,0.99805826,0.0000038801277,0.000085469845,0.0004472073,0.00003195886,0.00017894886,0.0008540064,0.00008775961,0.00019443806,0.000003540276],"about_ca_topic_score_codex":0.0024689164,"about_ca_topic_score_gemma":0.0037028014,"teacher_disagreement_score":0.0024689164,"about_ca_system_score_codex":0.00018419,"about_ca_system_score_gemma":0.00016801585,"threshold_uncertainty_score":0.0054499507},"labels":[],"label_agreement":null},{"id":"W4388217354","doi":"10.1038/s41588-023-01527-3","title":"An atlas of genetic determinants of forearm fracture","year":2023,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Genetic Associations and Epidemiology","field":"Biochemistry, Genetics and Molecular Biology","cited_by":16,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"McGill University; Jewish General Hospital","funders":"National Research, Development and Innovation Office; European Regional Development Fund; Janssen Biotech; Medical Research Council; Genentech; Novo Nordisk Fonden; Faculty of Medicine and Health, University of Sydney; Svenska Läkaresällskapet; Göteborgs Universitet; Danmarks Frie Forskningsfond; Vetenskapsrådet; Fonden til Lægevidenskabens Fremme; Business Finland; Northwest Regional Development Agency; Knut och Alice Wallenbergs Stiftelse; Hungarian Scientific Research Fund; Magyar Tudományos Akadémia; Diabetes UK; Eesti Teadusagentuur; British Heart Foundation; Novo Nordisk; National Institute for Health and Care Research; Wellcome Trust; Cancer Research UK; Maze Therapeutics; Sanofi; Norges Teknisk-Naturvitenskapelige Universitet; Umeå Universitet; European Commission; Innovációs és Technológiai Minisztérium; Bristol-Myers Squibb; Kempe Foundation; Norwegian Institute of Public Health; Novartis; Celgene; Pfizer; Biogen; GlaxoSmithKline; AstraZeneca","keywords":"Biology; Atlas (anatomy); Forearm; Evolutionary biology; Genetics; Computational biology; Anatomy","score_opus":0.00906665292427615,"score_gpt":0.30256608441464344,"score_spread":0.2934994314903673,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4388217354","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.6155074,0.06408174,0.11050361,0.006864032,0.001214065,0.00029812282,0.1341834,0.003916793,0.06343082],"genre_scores_gemma":[0.83799237,0.02184925,0.05968245,0.0011463389,0.000756514,0.00029268613,0.058801636,0.00042659722,0.019052163],"study_design_codex":"design_other","study_design_gemma":"observational","domain_scores_codex":[0.9994375,0.000105326304,0.000041946605,0.00020583498,0.00015361923,0.000055780165],"domain_scores_gemma":[0.9989594,0.00026393417,0.00024295565,0.00016120286,0.00022416323,0.00014832488],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00059799163,0.0004969154,0.0005424424,0.004490906,0.0005161549,0.0009146629,0.00048088544,0.00047045472,0.01248412],"category_scores_gemma":[0.000890309,0.00023740201,0.0005849779,0.004250369,0.00030841862,0.00031785102,0.00087278784,0.000673315,0.002077219],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0023177431,0.00017267671,0.37222752,0.001274204,0.0019300166,0.00439765,0.00050898234,0.009877956,0.13185565,0.022413567,0.07605717,0.37696686],"study_design_scores_gemma":[0.000076315744,0.00025955186,0.8172477,0.00019248198,0.0004377245,0.006386391,0.00017558674,0.003921681,0.00824866,0.01860917,0.14435747,0.000087289074],"about_ca_topic_score_codex":0.0039320085,"about_ca_topic_score_gemma":0.004656465,"teacher_disagreement_score":0.01248412,"about_ca_system_score_codex":0.0005700706,"about_ca_system_score_gemma":0.00039124058,"threshold_uncertainty_score":0.041763604},"labels":[],"label_agreement":null},{"id":"W4388541037","doi":"10.1038/s41588-023-01534-4","title":"Characterizing prostate cancer risk through multi-ancestry genome-wide discovery of 187 novel risk variants","year":2023,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Genetic Associations and Epidemiology","field":"Biochemistry, Genetics and Molecular Biology","cited_by":143,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Alberta; University of Toronto; Princess Margaret Cancer Centre","funders":"Common Fund; Division of Cancer Epidemiology and Genetics, National Cancer Institute; DOD Prostate Cancer Research Program; Hellenic Health Foundation; National Institute of Arthritis and Musculoskeletal and Skin Diseases; National Cancer Institute; Ellison Medical Foundation; Instituto de Salud Carlos III; World Cancer Research Fund; Prostate Cancer Foundation; Medical Research Council; Eunice Kennedy Shriver National Institute of Child Health and Human Development; U.S. Department of Health and Human Services; University of California, San Francisco; National Institute for Health and Care Research; Vlaamse regering; Novo Nordisk Fonden; Fondation de France; National Health and Medical Research Council; Universiti Malaya; Prostate Cancer Foundation of Australia; Vetenskapsrådet; National Institute of Mental Health; KU Leuven; Canadian Institutes of Health Research; Fonds Wetenschappelijk Onderzoek; Cancerfonden; Breast Cancer Research Foundation; University of Cambridge; U.S. Department of Defense; Cancer Research UK; Australian Government; Ovarian Cancer Research Fund; Bundesministerium für Bildung und Forschung; Swedish Cancer Foundation; Deutsches Krebsforschungszentrum; Associazione Italiana per la Ricerca sul Cancro; National Center for Advancing Translational Sciences; Kaiser Permanente; Fondation ARC pour la Recherche sur le Cancer; National Cancer Research Institute; Royal Marsden NHS Foundation Trust; European Commission; Cancer Council Victoria; Deutsche Krebshilfe; Office of Research and Development; National Institute on Aging; Wayne and Gladys Valley Foundation; Institut National Du Cancer; Cancer Research Institute; National Institutes of Health; Robert Wood Johnson Foundation","keywords":"Prostate cancer; Biology; Genome-wide association study; Disease; Genetic genealogy; Genetics; Genetic association; 1000 Genomes Project; Cancer; Ancestry-informative marker; Prostate; Single-nucleotide polymorphism; Oncology; Genotype; Internal medicine; Gene; Medicine; Population; Environmental health","score_opus":0.019614922791592198,"score_gpt":0.30055600510231906,"score_spread":0.28094108231072684,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4388541037","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9985373,0.00023902954,0.0008793896,0.00002796126,0.0000026978582,0.0000058657115,0.00017611205,0.0000085798365,0.00012308093],"genre_scores_gemma":[0.9987953,0.00008278715,0.0008826171,0.000014077606,0.0000044696726,0.000003253223,0.00014749287,0.0000040883865,0.00006586817],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9995401,0.0001301863,0.00003430837,0.00016230479,0.00008159921,0.00005151485],"domain_scores_gemma":[0.99924916,0.00024393076,0.00029693524,0.000112003356,0.000036169764,0.00006169542],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00063077855,0.0002583264,0.00032669047,0.00080163626,0.00034468278,0.00043402953,0.00023291435,0.00030343997,0.00080829195],"category_scores_gemma":[0.0016987514,0.00018172765,0.00046520375,0.00090007915,0.0002482038,0.00015414113,0.0005438679,0.00044447277,0.00010072562],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0004569508,0.00004533066,0.9436431,0.00005612053,0.0007467383,0.0005659498,0.00041328094,0.00069231837,0.03716793,0.00022608122,0.000158236,0.015827902],"study_design_scores_gemma":[0.00003187378,0.00010940078,0.99334323,0.00001226778,0.00026164216,0.001173547,0.000086222026,0.0009358799,0.0031744232,0.00022959408,0.00063148496,0.000010420509],"about_ca_topic_score_codex":0.0018998808,"about_ca_topic_score_gemma":0.0032161388,"teacher_disagreement_score":0.0018998808,"about_ca_system_score_codex":0.00013290385,"about_ca_system_score_gemma":0.00016378642,"threshold_uncertainty_score":0.0037776828},"labels":[],"label_agreement":null},{"id":"W4388824157","doi":"10.1038/s41588-023-01563-z","title":"Multi-ancestry genome-wide association study of cannabis use disorder yields insight into disease biology and public health implications","year":2023,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Cannabis and Cannabinoid Research","field":"Medicine","cited_by":116,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Public Health Ontario; University of Toronto","funders":"National Center for Advancing Translational Sciences; National Institute of Mental Health; National Center for PTSD, U.S. Department of Veterans Affairs; National Institutes of Health; Foundation for the National Institutes of Health; Novo Nordisk Fonden; Lundbeckfonden; Aarhus Universitet; European Commission; National Institute on Alcohol Abuse and Alcoholism; One Mind; National Institute on Deafness and Other Communication Disorders; National Institute on Drug Abuse; National Alliance for Research on Schizophrenia and Depression; Novo Nordisk; VISN 4 Mental Illness Research, Education, and Clinical Center; Office of Research and Development; NIH Clinical Center; H. Lundbeck A/S; U.S. Department of Veterans Affairs; Brain and Behavior Research Foundation","keywords":"Biology; Genome-wide association study; Disease; Cannabis; Genetics; Genetic association; Genome; Public health; Association (psychology); Computational biology; Evolutionary biology; Genotype; Single-nucleotide polymorphism; Gene; Psychiatry","score_opus":0.04158225714365922,"score_gpt":0.36936439648022507,"score_spread":0.32778213933656586,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4388824157","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9938962,0.0014164915,0.0027453776,0.0002937406,0.000024900512,0.000011039277,0.00058181444,0.00003514443,0.0009954114],"genre_scores_gemma":[0.9982817,0.00024022783,0.0010713951,0.000037932867,0.000013294878,0.0000037030184,0.00014475183,0.0000067942206,0.0002001366],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99932694,0.0003140351,0.000045122895,0.00016775042,0.000072567,0.00007354532],"domain_scores_gemma":[0.9988808,0.0004747824,0.00022732369,0.00024983173,0.0000699209,0.00009735172],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0011390445,0.00032986392,0.00039178284,0.0011957478,0.00064551696,0.0007078585,0.0003327232,0.00047297904,0.002929721],"category_scores_gemma":[0.0021082247,0.00020088402,0.0009206938,0.0012927473,0.0003081958,0.00024530586,0.00083515234,0.0006134456,0.0001982167],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0005532887,0.00008175115,0.96464133,0.00006617192,0.002094307,0.00042988395,0.00019667383,0.0006306206,0.017371394,0.0005695426,0.0003282585,0.013036772],"study_design_scores_gemma":[0.00002700278,0.00009159654,0.9927827,0.000025852749,0.000887132,0.0004279985,0.00015796923,0.001611233,0.0021837605,0.00079289137,0.0010015079,0.000010310578],"about_ca_topic_score_codex":0.0052096127,"about_ca_topic_score_gemma":0.010882312,"teacher_disagreement_score":0.0052096127,"about_ca_system_score_codex":0.0001895932,"about_ca_system_score_gemma":0.00029532856,"threshold_uncertainty_score":0.010358632},"labels":[],"label_agreement":null},{"id":"W4389108274","doi":"10.1038/s41588-026-02586-y","title":"H3K27me3 spreading organizes canonical PRC1 chromatin architecture to regulate developmental programs","year":2023,"lang":"en","type":"preprint","venue":"Nature Genetics","topic":"Epigenetics and DNA Methylation","field":"Biochemistry, Genetics and Molecular Biology","cited_by":5,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Université de Montréal; Centre Hospitalier Universitaire Sainte-Justine; Alberta Children's Hospital; McGill University Health Centre; University of Toronto; Jewish General Hospital; Hospital for Sick Children; McGill Genome Centre; University of Calgary; McGill University","funders":"Fonds de Recherche du Québec - Santé; Natural Sciences and Engineering Research Council of Canada; Fondation Charles-Bruneau; National Institutes of Health; Government of Canada; Government of Ontario; St. Jude Children's Research Hospital; Compute Canada; Canadian Institutes of Health Research; Genome Canada","keywords":"Chromatin; Architecture; Computer science; Biology; Communication; Psychology; Genetics; History; DNA","score_opus":0.017618499288907383,"score_gpt":0.2874091932468745,"score_spread":0.26979069395796706,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4389108274","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.90298903,0.0012551564,0.07454836,0.00038132974,0.00016277951,0.000023604309,0.0008495376,0.0014820913,0.018308163],"genre_scores_gemma":[0.9854197,0.00031326633,0.0051535526,0.000058229143,0.000025375963,0.00001072555,0.00046247567,0.00029340404,0.008263235],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.99987423,0.0000065216946,0.0000031674422,0.00003920099,0.00004096601,0.000035753852],"domain_scores_gemma":[0.99988914,0.000016222797,0.000018222932,0.000026964284,0.000021537222,0.000027871396],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0001837024,0.0002858614,0.00022946601,0.0002928377,0.00021142745,0.00083349046,0.0004219062,0.00031473397,0.0041782144],"category_scores_gemma":[0.00039001522,0.00039072416,0.00027398643,0.00029157984,0.0003456102,0.00043088477,0.00065616175,0.00047131904,0.0020215116],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0002274202,0.000012806918,0.00370762,0.00005743528,0.000029670027,0.00014459541,0.00006334509,0.0029036298,0.9680904,0.007057311,0.001219405,0.016486282],"study_design_scores_gemma":[0.000052111747,0.00005974755,0.040941883,0.000009616125,0.000035770612,0.000311936,0.0000980594,0.046914686,0.89389765,0.0088548325,0.008791707,0.000032023134],"about_ca_topic_score_codex":0.0011218613,"about_ca_topic_score_gemma":0.0024403238,"teacher_disagreement_score":0.0041782144,"about_ca_system_score_codex":0.0005212784,"about_ca_system_score_gemma":0.0002650612,"threshold_uncertainty_score":0.013977587},"labels":[],"label_agreement":null},{"id":"W4389168138","doi":"10.1038/s41588-023-01569-7","title":"East Asian-specific and cross-ancestry genome-wide meta-analyses provide mechanistic insights into peptic ulcer disease","year":2023,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Helicobacter pylori-related gastroenterology studies","field":"Medicine","cited_by":21,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"McGill University","funders":"Alliance de recherche numérique du Canada; Ministry of Education, Culture, Sports, Science and Technology; University of Tokyo; Japan Agency for Medical Research and Development","keywords":"Biology; Helicobacter pylori; Genome-wide association study; Disease; Locus (genetics); Genetic architecture; Stomach; Etiology; Genetics; Gene; Internal medicine; Single-nucleotide polymorphism; Medicine; Phenotype; Genotype","score_opus":0.0686625503705549,"score_gpt":0.34546393036643835,"score_spread":0.27680137999588345,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4389168138","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.736474,0.24335639,0.010986072,0.0017684863,0.0004523223,0.00007743424,0.0035699243,0.00017222614,0.0031431813],"genre_scores_gemma":[0.9874938,0.009712813,0.0014218857,0.00028044873,0.00010846892,0.000026834246,0.00069035304,0.00002744211,0.00023798243],"study_design_codex":"observational","study_design_gemma":"meta_analysis","domain_scores_codex":[0.99697053,0.0013604421,0.00031241355,0.0009071153,0.00021004018,0.000239425],"domain_scores_gemma":[0.9967384,0.0017563634,0.00045929343,0.0006621613,0.00018823892,0.00019569717],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0044999155,0.0012013344,0.0018482483,0.0023241893,0.0006771016,0.001733461,0.0006875549,0.00081302726,0.0022039844],"category_scores_gemma":[0.0056599886,0.00048475293,0.0074353726,0.0033194749,0.00042364118,0.00065208896,0.0011970418,0.0010870742,0.00015505865],"study_design_candidate":"meta_analysis","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0019191887,0.000042332944,0.74964035,0.0027118626,0.21426332,0.0008728698,0.00027859124,0.0014631704,0.004161651,0.0007383655,0.0011249885,0.022783373],"study_design_scores_gemma":[0.00017212494,0.00028101922,0.7776719,0.00052440976,0.20904076,0.00079733203,0.0003806297,0.002679486,0.0011258594,0.0019925158,0.00529472,0.00003925886],"about_ca_topic_score_codex":0.0045485897,"about_ca_topic_score_gemma":0.007952235,"teacher_disagreement_score":0.0045485897,"about_ca_system_score_codex":0.00038005857,"about_ca_system_score_gemma":0.00054538035,"threshold_uncertainty_score":0.023798108},"labels":[],"label_agreement":null},{"id":"W4389174422","doi":"10.1038/s41588-023-01524-6","title":"Benchmarking of deep neural networks for predicting personal gene expression from DNA sequence highlights shortcomings","year":2023,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Genomics and Chromatin Dynamics","field":"Biochemistry, Genetics and Molecular Biology","cited_by":114,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Canadian Institute for Advanced Research","funders":"National Institute on Aging","keywords":"Benchmarking; Biology; Computational biology; DNA sequencing; Gene; Genetics; Personal genomics; Genome; Genomics; Human genome","score_opus":0.008019904422525752,"score_gpt":0.2400583485352147,"score_spread":0.23203844411268895,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4389174422","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.7024115,0.0054394267,0.2591761,0.0031876934,0.0007971886,0.00010719751,0.003642075,0.010769126,0.014469706],"genre_scores_gemma":[0.94414943,0.0006193793,0.046545766,0.0003456342,0.00005891792,0.00006391645,0.0043991306,0.00026182734,0.003556065],"study_design_codex":"simulation_or_modeling","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9988691,0.00035869426,0.00007026607,0.00028277666,0.00028935168,0.00012972919],"domain_scores_gemma":[0.99764997,0.001097964,0.00006286418,0.00045562818,0.00063669536,0.00009673777],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0025838607,0.0010108236,0.0007570628,0.0005688228,0.00033816686,0.0013113056,0.0015077824,0.0011224535,0.0025746417],"category_scores_gemma":[0.0074243373,0.00036323964,0.00054103404,0.0009036383,0.00044568576,0.0014957985,0.0008344766,0.001377579,0.000953212],"study_design_candidate":"bench_or_experimental","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00046595643,0.00021911788,0.008397292,0.00018061709,0.00027247827,0.0000771071,0.000044643362,0.7536009,0.008153098,0.0035832222,0.010145112,0.21486047],"study_design_scores_gemma":[0.000011874867,0.00005786545,0.0009407851,0.000014304944,0.000015956539,0.000014515256,0.000016775464,0.9913374,0.0044257236,0.002286268,0.0008713358,0.000007081616],"about_ca_topic_score_codex":0.016099483,"about_ca_topic_score_gemma":0.018373951,"teacher_disagreement_score":0.016099483,"about_ca_system_score_codex":0.0011803905,"about_ca_system_score_gemma":0.0013676872,"threshold_uncertainty_score":0.03201157},"labels":[],"label_agreement":null},{"id":"W4389391230","doi":"10.1038/s41588-023-01608-3","title":"Inferring compound heterozygosity from large-scale exome sequencing data","year":2023,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Genomics and Rare Diseases","field":"Biochemistry, Genetics and Molecular Biology","cited_by":35,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Université de Montréal; McGill Genome Centre; Montreal Heart Institute; University of Ottawa","funders":"National Institute of Diabetes and Digestive and Kidney Diseases; Eisai; National Human Genome Research Institute; GlaxoSmithKline; Biogen; Astellas Pharma; Wellcome Trust; U.S. Department of Health and Human Services","keywords":"Biology; Genetics; Exome sequencing; Exome; Compound heterozygosity; Gene; Computational biology; Loss of heterozygosity; Mendelian inheritance; 1000 Genomes Project; Context (archaeology); Genome; Whole genome sequencing; Genotype; Allele; Mutation; Single-nucleotide polymorphism","score_opus":0.024461095510509796,"score_gpt":0.285495727216693,"score_spread":0.2610346317061832,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4389391230","genre_codex":"empirical","genre_gemma":"methods","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"methods","genre_consensus":null,"domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.66979766,0.0019023613,0.31057552,0.00069663563,0.00009593584,0.00012389317,0.014202466,0.0015882497,0.0010172982],"genre_scores_gemma":[0.88899696,0.0008445675,0.09420189,0.0002748179,0.00012254438,0.000057642595,0.014764707,0.0001773488,0.0005595252],"study_design_codex":"observational","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9987942,0.00030303077,0.00011676105,0.0004694688,0.00019963701,0.00011685429],"domain_scores_gemma":[0.9931791,0.005405472,0.0005202769,0.00040812744,0.00027217215,0.000214844],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0027338918,0.0012224424,0.0014839019,0.003594065,0.00044845432,0.0017777745,0.0010155772,0.0012183174,0.0012860837],"category_scores_gemma":[0.010477151,0.0007708318,0.0013695329,0.0020227558,0.00043687047,0.0014180744,0.0013734795,0.0012424932,0.0006161022],"study_design_candidate":"bench_or_experimental","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0017728425,0.0005590818,0.512534,0.0010104093,0.0032318144,0.011390833,0.00039901736,0.119174436,0.1337382,0.006910965,0.0062929103,0.20298542],"study_design_scores_gemma":[0.0003858804,0.00041716875,0.18110295,0.0001943691,0.0019657128,0.009624497,0.00049730216,0.69237596,0.026911873,0.079261966,0.007052229,0.00021011941],"about_ca_topic_score_codex":0.002422438,"about_ca_topic_score_gemma":0.0053119455,"teacher_disagreement_score":0.003594065,"about_ca_system_score_codex":0.000294159,"about_ca_system_score_gemma":0.0010330944,"threshold_uncertainty_score":0.014458358},"labels":[],"label_agreement":null},{"id":"W4389488172","doi":"10.1038/s41588-023-01588-4","title":"CellCharter reveals spatial cell niches associated with tissue remodeling and cell plasticity","year":2023,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Single-cell and spatial transcriptomics","field":"Biochemistry, Genetics and Molecular Biology","cited_by":177,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"McGill University","funders":"","keywords":"Biology; Niche; Ecological niche; Cell; Computational biology; Lung cancer; Genetics; Pathology; Ecology; Medicine","score_opus":0.00929937828454016,"score_gpt":0.2228931560911985,"score_spread":0.21359377780665834,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4389488172","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.91529936,0.0011367669,0.07362443,0.00059050584,0.00018494843,0.000046901987,0.0022893797,0.0019223662,0.0049053305],"genre_scores_gemma":[0.9547841,0.00050338847,0.03011396,0.00030800555,0.000042682095,0.000073923875,0.0017677111,0.0014693633,0.010936891],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9995296,0.000027985468,0.000018065088,0.00014989123,0.00017761956,0.00009671228],"domain_scores_gemma":[0.9993173,0.00022807004,0.0001303196,0.000113049064,0.00006722412,0.00014408347],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00041468046,0.00032912477,0.00042565953,0.00079648744,0.000633733,0.0016930769,0.00075907685,0.0008536368,0.0043632477],"category_scores_gemma":[0.0004983007,0.00057099096,0.00036317247,0.0003659865,0.00063012866,0.0009536022,0.0008924349,0.0014507185,0.001235579],"study_design_candidate":"bench_or_experimental","study_design_consensus":"bench_or_experimental","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00006932754,0.00000911126,0.00038731095,0.000015178896,0.0000028313877,0.000056611072,0.000017409066,0.00022516816,0.9959347,0.0012015263,0.00016942435,0.0019113519],"study_design_scores_gemma":[0.00002711178,0.000032535314,0.011671552,0.000007898199,0.000012310938,0.0003544113,0.00005869569,0.012600523,0.9682252,0.0010100473,0.005972322,0.00002738173],"about_ca_topic_score_codex":0.0012410377,"about_ca_topic_score_gemma":0.005031702,"teacher_disagreement_score":0.0043632477,"about_ca_system_score_codex":0.00078837294,"about_ca_system_score_gemma":0.00055431185,"threshold_uncertainty_score":0.014596462},"labels":[],"label_agreement":null},{"id":"W4390345401","doi":"10.1038/s41588-023-01584-8","title":"Multi-ancestry genome-wide association meta-analysis of Parkinson’s disease","year":2023,"lang":"en","type":"review","venue":"Nature Genetics","topic":"Parkinson's Disease Mechanisms and Treatments","field":"Medicine","cited_by":259,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"McGill University; Institut Universitaire de Gériatrie de Montréal; Montreal Neurological Institute and Hospital","funders":"Innovate UK; National Medical Research Council; National Institute of Neurological Disorders and Stroke; Medical Research Council; Barts Charity; National Institute on Aging; Ministry of Education - Singapore; Parkinson's Foundation; Michael J. Fox Foundation for Parkinson's Research; National Institutes of Health; U.S. Department of Health and Human Services","keywords":"Biology; Genome-wide association study; Genetic association; Expression quantitative trait loci; Genetics; Meta-analysis; Disease; Population; Genome; Imputation (statistics); 1000 Genomes Project; Single-nucleotide polymorphism; Gene; Genotype; Missing data; Medicine; Internal medicine; Environmental health","score_opus":0.11381687640331765,"score_gpt":0.3812743717450449,"score_spread":0.26745749534172725,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4390345401","genre_codex":"review","genre_gemma":"review","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"review","genre_consensus":"review","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.0010106823,0.99812156,0.0003059251,0.00018902001,0.000073731455,0.000010398291,0.00011550992,0.000011973772,0.00016124317],"genre_scores_gemma":[0.022558864,0.9751413,0.0011500412,0.00035545605,0.00014177736,0.000042058215,0.00041797472,0.0000108442355,0.00018166505],"study_design_codex":"design_other","study_design_gemma":"meta_analysis","domain_scores_codex":[0.99896073,0.00045664248,0.00016449793,0.00019654658,0.000158396,0.00006317921],"domain_scores_gemma":[0.99821055,0.0012876843,0.0001859649,0.00008190923,0.00018472511,0.00004920526],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0034861849,0.0014603887,0.0050780633,0.002188162,0.0002042084,0.0010204463,0.0010009906,0.00093148684,0.0019063805],"category_scores_gemma":[0.004074456,0.00046244884,0.0071148267,0.0030142155,0.00018391553,0.00048738302,0.00071110466,0.001195232,0.0002866605],"study_design_candidate":"meta_analysis","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0032435893,0.000071835384,0.01483558,0.15268654,0.26520014,0.0005725417,0.000103014114,0.0024456196,0.0017747725,0.0015266804,0.012156404,0.54538333],"study_design_scores_gemma":[0.001474357,0.0009232715,0.06432177,0.037756626,0.74621403,0.0026284019,0.00015718736,0.0020330967,0.0019455343,0.0068279533,0.13554351,0.00017432755],"about_ca_topic_score_codex":0.0030019158,"about_ca_topic_score_gemma":0.0076064593,"teacher_disagreement_score":0.0050780633,"about_ca_system_score_codex":0.0007781327,"about_ca_system_score_gemma":0.0014832316,"threshold_uncertainty_score":0.018436909},"labels":[],"label_agreement":null},{"id":"W4391350860","doi":"10.1038/s41588-024-01653-6","title":"Cell-type-specific CAG repeat expansions and toxicity of mutant Huntingtin in human striatum and cerebellum","year":2024,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Genetic Neurodegenerative Diseases","field":"Neuroscience","cited_by":133,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Toronto; Université Laval; Hospital for Sick Children","funders":"National Institute on Aging; Natural Sciences and Engineering Research Council of Canada; Canadian Institutes of Health Research; University of Washington; CHDI Foundation; University of Michigan; Cure Huntington's Disease Initiative; National Institutes of Health; Government of Canada; Hereditary Disease Foundation; Sigrid Juséliuksen Säätiö; U.S. Department of Veterans Affairs","keywords":"Biology; Huntingtin; Cerebellum; Striatum; Huntington's disease; Cell biology; Somatic cell; Mutant; Medium spiny neuron; Huntingtin Protein; Programmed cell death; Polyglutamine tract; Trinucleotide repeat expansion; Purkinje cell; Neurodegeneration; Molecular biology; Neuroscience; Genetics; Apoptosis; Gene; Internal medicine","score_opus":0.020537224627872674,"score_gpt":0.27699744159116824,"score_spread":0.2564602169632956,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4391350860","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9984682,0.00048602844,0.00039506957,0.000010718748,0.0000012889664,0.0000036725332,0.00013900085,0.000012726266,0.00048325304],"genre_scores_gemma":[0.9985953,0.00026429686,0.00043359125,0.000013372615,0.0000011483854,0.0000051737184,0.00028100412,0.0000046809164,0.000401465],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9999349,0.0000049549644,0.0000068097042,0.000022380349,0.000020807453,0.000010061826],"domain_scores_gemma":[0.999949,0.000004697071,0.00002169558,0.0000044623403,0.000005857843,0.00001431165],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00007704039,0.00012395522,0.00014732988,0.0003136996,0.00009394994,0.0001820912,0.000062411484,0.000136466,0.0004366735],"category_scores_gemma":[0.000082841114,0.00010956667,0.00009870859,0.00014529329,0.00015980095,0.00006764886,0.00015755746,0.000103785314,0.00007263236],"study_design_candidate":"bench_or_experimental","study_design_consensus":"bench_or_experimental","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00009958223,0.000009810377,0.009823003,0.000017283555,0.000020067448,0.00023437686,0.000049689956,0.00006652346,0.98806167,0.000072176386,0.00002429741,0.0015216261],"study_design_scores_gemma":[0.00001771885,0.00031892792,0.7215389,0.000010606362,0.00008050253,0.005561122,0.00014988062,0.0011596853,0.26994804,0.00024400219,0.0009606224,0.000009873619],"about_ca_topic_score_codex":0.0020502587,"about_ca_topic_score_gemma":0.004869686,"teacher_disagreement_score":0.0020502587,"about_ca_system_score_codex":0.00016460556,"about_ca_system_score_gemma":0.00011970514,"threshold_uncertainty_score":0.0040767193},"labels":[],"label_agreement":null},{"id":"W4391652876","doi":"10.1038/s41588-023-01642-1","title":"Advancing diagnosis and research for rare genetic diseases in Indigenous peoples","year":2024,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Genomics and Rare Diseases","field":"Biochemistry, Genetics and Molecular Biology","cited_by":14,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Northern British Columbia; University of British Columbia; Institute of Genetics; Canadian Institutes of Health Research; Dalhousie University","funders":"National Institutes of Health; National Human Genome Research Institute; Institut National de la Santé et de la Recherche Médicale; European Commission","keywords":"Indigenous; Biology; Disease; Task force; Rare disease; Political science; Medicine; Ecology; Pathology; Public administration","score_opus":0.008715382933306879,"score_gpt":0.31391312480268935,"score_spread":0.3051977418693825,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4391652876","genre_codex":"commentary","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":null,"domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.327792,0.18387625,0.02362893,0.39964548,0.0074207177,0.00027080948,0.0014576039,0.0005783675,0.0553298],"genre_scores_gemma":[0.7491241,0.13721716,0.040019996,0.053274095,0.012441166,0.00017805943,0.0006752662,0.00010525875,0.006964893],"study_design_codex":"design_other","study_design_gemma":"theoretical_or_conceptual","domain_scores_codex":[0.9971419,0.001098478,0.00025794742,0.0002946029,0.00079629314,0.0004107089],"domain_scores_gemma":[0.97931826,0.009021067,0.0019405272,0.00089051627,0.0053097014,0.0035198776],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.010365965,0.0003618354,0.0006717821,0.002534171,0.0012680836,0.002447955,0.0013026946,0.0019649393,0.004514303],"category_scores_gemma":[0.02293177,0.00022054305,0.00055702945,0.0012526464,0.0018325277,0.002421249,0.003136663,0.002686361,0.000963355],"study_design_candidate":"theoretical_or_conceptual","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00035806745,0.00065874634,0.26982647,0.0026356312,0.0002603414,0.0021287946,0.010041226,0.00059621845,0.012482005,0.016019411,0.04048843,0.6445046],"study_design_scores_gemma":[0.00028931422,0.0009861964,0.5385876,0.008651784,0.0010064937,0.0065393383,0.028355435,0.0018146283,0.0058780336,0.07789918,0.32978913,0.00020293193],"about_ca_topic_score_codex":0.028844105,"about_ca_topic_score_gemma":0.031075323,"teacher_disagreement_score":0.028844105,"about_ca_system_score_codex":0.0021960188,"about_ca_system_score_gemma":0.01024776,"threshold_uncertainty_score":0.057352424},"labels":[],"label_agreement":null},{"id":"W4392198237","doi":"10.1038/s41588-024-01664-3","title":"BANKSY unifies cell typing and tissue domain segmentation for scalable spatial omics data analysis","year":2024,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Single-cell and spatial transcriptomics","field":"Biochemistry, Genetics and Molecular Biology","cited_by":224,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Artificial Intelligence in Medicine (Canada)","funders":"Graduiertenakademie, Technische Universität Dresden; National Research Foundation Singapore; National Medical Research Council; Medical Research Council; Agency for Science, Technology and Research; National Research Foundation","keywords":"Biology; Computational biology; Segmentation; Domain (mathematical analysis); Scalability; Spatial analysis; Evolutionary biology; Computer science; Artificial intelligence; Database; Remote sensing","score_opus":0.012964715872633432,"score_gpt":0.27704063301888426,"score_spread":0.26407591714625084,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4392198237","genre_codex":"methods","genre_gemma":"methods","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"methods","genre_consensus":"methods","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.010970279,0.0001484631,0.973244,0.00015793178,0.000044065608,0.00006984428,0.0006362916,0.014154012,0.0005752514],"genre_scores_gemma":[0.08529782,0.00017223577,0.9068921,0.00019740131,0.000064606895,0.00028019937,0.0026062157,0.0022243906,0.0022650405],"study_design_codex":"design_other","study_design_gemma":"simulation_or_modeling","domain_scores_codex":[0.99852306,0.00023536659,0.00011505275,0.00040750162,0.0005881643,0.00013086575],"domain_scores_gemma":[0.99743855,0.0007868362,0.00018648646,0.000975067,0.00042403035,0.00018912897],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.002235433,0.001290485,0.0016402502,0.0017411702,0.00089453,0.0019368264,0.0023656534,0.0014856714,0.003403177],"category_scores_gemma":[0.0053714192,0.0010643627,0.002205773,0.0017187552,0.0015312386,0.0022421093,0.0051588304,0.0019645847,0.0029492527],"study_design_candidate":"simulation_or_modeling","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0008709204,0.00020258217,0.0097748665,0.0004599973,0.00047595307,0.00055339624,0.000686082,0.23666066,0.17575616,0.031477675,0.041186195,0.5018955],"study_design_scores_gemma":[0.00004833624,0.00008761765,0.0016649021,0.0000179383,0.000033805554,0.00018498876,0.000079240315,0.91458446,0.05023749,0.01801983,0.014991038,0.00005034804],"about_ca_topic_score_codex":0.00676036,"about_ca_topic_score_gemma":0.011754334,"teacher_disagreement_score":0.00676036,"about_ca_system_score_codex":0.0011975123,"about_ca_system_score_gemma":0.0027349659,"threshold_uncertainty_score":0.0134420395},"labels":[],"label_agreement":null},{"id":"W4392294702","doi":"10.1038/s41588-024-01668-z","title":"Epigenetic variation impacts individual differences in the transcriptional response to influenza infection","year":2024,"lang":"en","type":"article","venue":"Nature Genetics","topic":"RNA modifications and cancer","field":"Biochemistry, Genetics and Molecular Biology","cited_by":40,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"McGill Genome Centre; Centre Hospitalier Universitaire Sainte-Justine; McGill University","funders":"National Institute of General Medical Sciences; U.S. Department of Health and Human Services","keywords":"Epigenetics; Biology; Quantitative trait locus; Genetics; Expression quantitative trait loci; Genetic variation; Phenotype; Gene; Locus (genetics); Gene expression; Influenza A virus; Gene expression profiling; Regulation of gene expression; Virus; Single-nucleotide polymorphism; Genotype","score_opus":0.01991086786592724,"score_gpt":0.3048195226186022,"score_spread":0.28490865475267496,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4392294702","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99853754,0.000088320005,0.000488127,0.000046512756,0.00001528823,0.000004718059,0.00020248759,0.00001184422,0.0006051851],"genre_scores_gemma":[0.99889946,0.00004443305,0.00018604088,0.000054217046,0.000005303093,0.000006579162,0.00009831886,0.000018210087,0.00068731135],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9997731,0.000053590695,0.000013200192,0.000081738726,0.000033828575,0.00004456153],"domain_scores_gemma":[0.9997044,0.000083291445,0.000063757034,0.000049085607,0.000036900343,0.000062484585],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00027829537,0.00011809766,0.0002330974,0.00026196093,0.0001328547,0.0003029893,0.00019552586,0.0003313693,0.002184545],"category_scores_gemma":[0.0006184469,0.0001877106,0.00019277484,0.00018247985,0.00022587007,0.0001367042,0.0002756397,0.0004042698,0.00025653027],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0011897581,0.0000727081,0.031675752,0.000026549584,0.00017444626,0.00007487087,0.000185828,0.0003954492,0.95758396,0.00029652638,0.00027017063,0.0080540525],"study_design_scores_gemma":[0.000027654163,0.0004007999,0.9132637,0.000009662377,0.00011774126,0.0003710436,0.00025828672,0.0024012313,0.08158232,0.0004724438,0.0010604115,0.000034870067],"about_ca_topic_score_codex":0.0011345764,"about_ca_topic_score_gemma":0.0017341875,"teacher_disagreement_score":0.002184545,"about_ca_system_score_codex":0.00018069094,"about_ca_system_score_gemma":0.000089797,"threshold_uncertainty_score":0.0073080063},"labels":[],"label_agreement":null},{"id":"W4392748252","doi":"10.1038/s41588-024-01708-8","title":"Guidance on use of race, ethnicity, and geographic origin as proxies for genetic ancestry groups in biomedical publications","year":2024,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Ethics in Clinical Research","field":"Medicine","cited_by":11,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of British Columbia","funders":"","keywords":"Race (biology); Genetic genealogy; Biology; Ethnic group; Evolutionary biology; Demography; Genetics; Anthropology; Population; Sociology","score_opus":0.26444620740982056,"score_gpt":0.5368024186260452,"score_spread":0.2723562112162246,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4392748252","genre_codex":"commentary","genre_gemma":"methods","domain_codex":null,"domain_gemma":"methods","model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"methods","genre_consensus":null,"domain_candidate":"methods","domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.010252743,0.017736975,0.17397518,0.62954086,0.01955803,0.005766568,0.0028901002,0.0028455919,0.13743402],"genre_scores_gemma":[0.061106604,0.013377611,0.67622226,0.19048314,0.0057729,0.012123805,0.002165836,0.0016669112,0.037081033],"study_design_codex":"not_applicable","study_design_gemma":"not_applicable","domain_scores_codex":[0.5929974,0.26320088,0.081644155,0.0053320862,0.05068804,0.0061374633],"domain_scores_gemma":[0.22616532,0.5707501,0.03263615,0.027321575,0.13163483,0.011492056],"candidate_categories":["metaresearch","research_integrity"],"consensus_categories":["metaresearch"],"category_scores_codex":[0.25518885,0.0016031037,0.003318429,0.010775364,0.0059926077,0.015599002,0.007860614,0.024900256,0.010381227],"category_scores_gemma":[0.5145746,0.0035249407,0.004255183,0.008110377,0.0117202075,0.012168049,0.008595512,0.022557376,0.012126913],"study_design_candidate":"not_applicable","study_design_consensus":"not_applicable","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0003519698,0.0004145171,0.007523558,0.003405307,0.00020020055,0.0012984469,0.014987768,0.00076489715,0.0021511356,0.09554398,0.7084253,0.16493307],"study_design_scores_gemma":[0.0007892581,0.00026568846,0.013645641,0.03149202,0.00032472308,0.0036853172,0.0102849025,0.0027358865,0.003026342,0.107920356,0.825315,0.00051487325],"about_ca_topic_score_codex":0.012774862,"about_ca_topic_score_gemma":0.036089327,"teacher_disagreement_score":0.97509974,"about_ca_system_score_codex":0.0035974034,"about_ca_system_score_gemma":0.02940957,"threshold_uncertainty_score":0.91848475},"labels":[],"label_agreement":null},{"id":"W4393043838","doi":"10.1038/s41588-024-01685-y","title":"Cell subtype-specific effects of genetic variation in the Alzheimer’s disease brain","year":2024,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Genetic Associations and Epidemiology","field":"Biochemistry, Genetics and Molecular Biology","cited_by":178,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"BC Children's Hospital; University of British Columbia","funders":"National Institute of Diabetes and Digestive and Kidney Diseases; National Institute on Aging; National Institutes of Health; U.S. Department of Health and Human Services","keywords":"Biology; Disease; Genetic variation; Alzheimer's disease; Genetics; Variation (astronomy); Brain Cell; Neuroscience; Gene; Internal medicine","score_opus":0.007802312713669962,"score_gpt":0.2579395337321562,"score_spread":0.25013722101848623,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4393043838","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9980197,0.0005724797,0.00024389054,0.00011065436,0.000016405853,0.000003473392,0.00026741184,0.0000060862335,0.000759932],"genre_scores_gemma":[0.9985758,0.00033780732,0.00025122293,0.000049401926,0.000033598415,0.0000039181177,0.00017252605,0.000016050131,0.00055963226],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9992835,0.0002448997,0.00006619943,0.00020038731,0.00011099733,0.0000939535],"domain_scores_gemma":[0.9987821,0.00045325825,0.00031438333,0.00016793115,0.00016248219,0.00011991007],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0007903983,0.0003338881,0.00049629866,0.0015710128,0.0004068009,0.000786566,0.00058916723,0.00052794494,0.002963398],"category_scores_gemma":[0.0016903912,0.0003169396,0.0005465908,0.0009188552,0.0004698224,0.0003426183,0.00041297034,0.0005915742,0.00027353485],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0032929792,0.00021246905,0.851552,0.00008520132,0.001542134,0.0021175041,0.0011902933,0.0004357744,0.12039299,0.0016453916,0.0009014201,0.016631735],"study_design_scores_gemma":[0.000021962443,0.00007665902,0.9948526,0.000012799712,0.0001942306,0.0011835879,0.00029998453,0.0002500236,0.0018522562,0.0008965908,0.0003493025,0.000010068074],"about_ca_topic_score_codex":0.0061493423,"about_ca_topic_score_gemma":0.005945495,"teacher_disagreement_score":0.0061493423,"about_ca_system_score_codex":0.00030298496,"about_ca_system_score_gemma":0.00018682174,"threshold_uncertainty_score":0.012227118},"labels":[],"label_agreement":null},{"id":"W4393317597","doi":"10.1038/s41588-024-01686-x","title":"Comprehensive whole-genome sequence analyses provide insights into the genomic architecture of cerebral palsy","year":2024,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Neurogenetic and Muscular Disorders Research","field":"Medicine","cited_by":40,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Centre Hospitalier Universitaire Sainte-Justine; Children's Hospital Research Institute of Manitoba; University of Alberta; University of British Columbia; University of Manitoba; McMaster University; Ontario Genomics; Queen's University; Ted Rogers Centre for Heart Research; Thames Valley Children's Centre; University of Calgary; Children's Hospital of Eastern Ontario; McGill University; University of Ottawa; McGill University Health Centre; Université de Montréal; Hospital for Sick Children; University of Toronto; SickKids Foundation; BC Children's Hospital; Holland Bloorview Kids Rehabilitation Hospital","funders":"Hospital for Sick Children; Azrieli Foundation; Women and Children's Health Research Institute; Canadian Institutes of Health Research; AllerGen; Government of Canada; Fondation Brain Canada; Ontario Brain Institute","keywords":"Indel; Biology; Genetics; Copy-number variation; Gene; Genome; Whole genome sequencing; Genetic architecture; Mutation; Single-nucleotide polymorphism; Phenotype; Genotype","score_opus":0.037779366179116196,"score_gpt":0.35220684635719035,"score_spread":0.31442748017807415,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4393317597","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.95577556,0.0077355155,0.015734894,0.0008741824,0.00006271536,0.0000337471,0.015502341,0.00027647207,0.004004603],"genre_scores_gemma":[0.9733203,0.0054215915,0.007508987,0.0002876658,0.000056934077,0.00003177747,0.011793617,0.00009828783,0.0014809018],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9998286,0.000017195493,0.0000107372925,0.00006343343,0.000044389333,0.00003570486],"domain_scores_gemma":[0.9997569,0.00008997299,0.0000621906,0.000025534073,0.000030349283,0.000035026216],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00024092848,0.00040076787,0.0004851456,0.0014348386,0.0003911093,0.00063803344,0.00031809448,0.00049123087,0.0018042877],"category_scores_gemma":[0.0004815228,0.00022063771,0.00056564435,0.0013781184,0.0003734754,0.00026264717,0.0005011623,0.0006924731,0.00033376715],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.001041622,0.00010500924,0.08891479,0.00066080934,0.001004796,0.0029716662,0.0005983044,0.009517642,0.7954549,0.003553584,0.0032751048,0.092901826],"study_design_scores_gemma":[0.000050219867,0.00016594057,0.9270401,0.00014876775,0.00067457836,0.002210556,0.00047288864,0.0053385766,0.03658435,0.0061194766,0.021131763,0.00006287854],"about_ca_topic_score_codex":0.0065653757,"about_ca_topic_score_gemma":0.013907859,"teacher_disagreement_score":0.0065653757,"about_ca_system_score_codex":0.00035996153,"about_ca_system_score_gemma":0.0008707071,"threshold_uncertainty_score":0.013054311},"labels":[],"label_agreement":null},{"id":"W4394823558","doi":"10.1038/s41588-024-01695-w","title":"The genome and population genomics of allopolyploid Coffea arabica reveal the diversification history of modern coffee cultivars","year":2024,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Coffee research and impacts","field":"Medicine","cited_by":85,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Ottawa","funders":"Instituut voor Landbouw-, Visserij- en Voedingsonderzoek, Vlaamse Overheid; Vlaamse regering; Instituto Nacional de Ciência e Tecnologia do Café; Natural Sciences and Engineering Research Council of Canada; Fundação Araucária; Universiteit Gent; Fonds Wetenschappelijk Onderzoek; Institut de Recherche pour le Développement; Conselho Nacional de Desenvolvimento Científico e Tecnológico; Universitair Ziekenhuis Gent; Academy of Finland; Helsingin Yliopisto; Fundação de Amparo à Pesquisa do Estado de São Paulo; Nanyang Technological University; European Commission; Directorate for Biological Sciences; Canada Research Chairs; University at Buffalo; Universidade Tecnológica Federal do Paraná; National Science Foundation","keywords":"Biology; Coffea canephora; Coffea arabica; Domestication; Ploidy; Genomics; Genome; Population; Botany; Genetics; Gene","score_opus":0.0208827562971149,"score_gpt":0.28588893272563826,"score_spread":0.26500617642852337,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4394823558","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99483645,0.0008783951,0.0011515364,0.00008265435,0.000007528,0.0000046321416,0.0019688539,0.00008128317,0.0009886601],"genre_scores_gemma":[0.993731,0.0003656127,0.0019301729,0.0000619179,0.000008634272,0.000008840764,0.0030657048,0.000042752425,0.0007852351],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.99995327,0.000003865764,0.0000024688516,0.000027637183,0.000006136008,0.0000066401394],"domain_scores_gemma":[0.9998754,0.000023951414,0.00004525362,0.000014426841,0.0000145726835,0.000026305432],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.000097378295,0.00019291237,0.00013474366,0.00059771125,0.00031264054,0.0003594951,0.0001125581,0.0002335617,0.0022109349],"category_scores_gemma":[0.0003082299,0.00008945147,0.00020713876,0.0006676252,0.00013029744,0.000238897,0.0002874446,0.00032144756,0.00024805855],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00053341215,0.00003298343,0.07913934,0.00026475688,0.00017490769,0.00035813233,0.0014867762,0.0010143671,0.87356293,0.0007490575,0.00069644535,0.041986953],"study_design_scores_gemma":[0.000008795553,0.00006485462,0.97298753,0.000029607385,0.00010174323,0.00061666174,0.0004159189,0.0016470037,0.012034101,0.00048265987,0.011590556,0.000020566666],"about_ca_topic_score_codex":0.0023243853,"about_ca_topic_score_gemma":0.0040508024,"teacher_disagreement_score":0.0023243853,"about_ca_system_score_codex":0.00021710453,"about_ca_system_score_gemma":0.000110041605,"threshold_uncertainty_score":0.0073963404},"labels":[],"label_agreement":null},{"id":"W4394924136","doi":"10.1038/s41588-024-01707-9","title":"Genome-wide association analyses identify 95 risk loci and provide insights into the neurobiology of post-traumatic stress disorder","year":2024,"lang":"en","type":"review","venue":"Nature Genetics","topic":"Stress Responses and Cortisol","field":"Neuroscience","cited_by":178,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Centre for Addiction and Mental Health; Public Health Ontario; University of Toronto","funders":"Congressionally Directed Medical Research Programs; Eunice Kennedy Shriver National Institute of Child Health and Human Development; National Institute on Minority Health and Health Disparities; Medical Research Council; National Center for Advancing Translational Sciences; National Human Genome Research Institute; National Institute of Mental Health; Stanley Center for Psychiatric Research, Broad Institute; ACADIA Pharmaceuticals; Genentech; Servier; Biogen; Cohen Veterans Bioscience; Cabrini Foundation; Eisai; Army Research Office; Jazz Pharmaceuticals; U.S. Department of Defense; Sanofi; Broad Institute; National Institutes of Health; U.S. Department of Health and Human Services; McCormick Foundation; Sage Therapeutics; Defense Advanced Research Projects Agency; H. Lundbeck A/S; U.S. Department of Veterans Affairs","keywords":"Genome-wide association study; Biology; Neuroscience; Genetic association; Genetics; Gene; Single-nucleotide polymorphism; Genotype","score_opus":0.0328232479679003,"score_gpt":0.3564170464430192,"score_spread":0.3235937984751189,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4394924136","genre_codex":"review","genre_gemma":"review","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"review","genre_consensus":"review","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.00009496706,0.99872357,0.00016484578,0.00031914312,0.00008099471,0.000002832914,0.00005713916,0.00001071277,0.00054565305],"genre_scores_gemma":[0.00090171956,0.9982255,0.00023120778,0.00017629447,0.000090662295,0.000005182284,0.00008097995,0.000002660718,0.0002857751],"study_design_codex":"design_other","study_design_gemma":"observational","domain_scores_codex":[0.99971277,0.00007138916,0.00004274321,0.000070321934,0.00007789468,0.000024727542],"domain_scores_gemma":[0.9991732,0.0005350907,0.00008959399,0.000022816388,0.00013427198,0.000045011268],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0011518345,0.0011819121,0.0018404804,0.0027324713,0.00016120635,0.00086627685,0.0009411595,0.001082159,0.00374247],"category_scores_gemma":[0.0016967424,0.00027137858,0.00080502086,0.0030517203,0.0004390778,0.0006414372,0.0005894992,0.0013981542,0.0018869665],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00013322313,0.000020677371,0.0008176569,0.0148240095,0.00064357684,0.00021151082,0.000036577992,0.0002875502,0.00067161646,0.0021996342,0.02495787,0.95519614],"study_design_scores_gemma":[0.00006705603,0.0001289686,0.008227297,0.012172917,0.0018997906,0.0023296205,0.00008877079,0.00017662211,0.00063456566,0.0054227123,0.96880317,0.000048402813],"about_ca_topic_score_codex":0.0021494054,"about_ca_topic_score_gemma":0.003981035,"teacher_disagreement_score":0.00374247,"about_ca_system_score_codex":0.00083651155,"about_ca_system_score_gemma":0.0013433447,"threshold_uncertainty_score":0.012519777},"labels":[],"label_agreement":null},{"id":"W4394943296","doi":"10.1038/s41588-024-01752-4","title":"Author Correction: New genetic signals for lung function highlight pathways and chronic obstructive pulmonary disease associations across multiple ancestries","year":2024,"lang":"en","type":"erratum","venue":"Nature Genetics","topic":"Chronic Obstructive Pulmonary Disease (COPD) Research","field":"Medicine","cited_by":0,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Institut universitaire de cardiologie et de pneumologie de Québec; Université Laval; St. Paul's Hospital; University of British Columbia","funders":"","keywords":"Biology; Pulmonary disease; Lung function; Computational biology; Disease; Genetics; Function (biology); Genome-wide association study; Lung; Lung disease; Bioinformatics; Gene; Internal medicine; Single-nucleotide polymorphism; Medicine; Genotype","score_opus":0.0203333702412756,"score_gpt":0.3129591006338193,"score_spread":0.2926257303925437,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4394943296","genre_codex":"editorial","genre_gemma":"other","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"other","genre_consensus":null,"domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.00021032438,0.0005057145,0.000947207,0.06282106,0.9311788,0.000022190532,0.0018674822,0.00045672397,0.001990625],"genre_scores_gemma":[0.029157173,0.005811219,0.012935974,0.17157735,0.45856208,0.00038975055,0.0066284984,0.0045820093,0.31035602],"study_design_codex":"not_applicable","study_design_gemma":"not_applicable","domain_scores_codex":[0.99582064,0.0008031393,0.0006727053,0.00068711216,0.0015189843,0.0004972919],"domain_scores_gemma":[0.9738563,0.009026026,0.001301197,0.0017156843,0.012586329,0.0015145359],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.004593602,0.0024194184,0.0020967068,0.0027964397,0.0032350805,0.0039035212,0.0039680838,0.007953706,0.08696977],"category_scores_gemma":[0.065783806,0.0013580059,0.0020452742,0.0018027861,0.002179209,0.0019291717,0.0022513878,0.011847766,0.034052353],"study_design_candidate":"not_applicable","study_design_consensus":"not_applicable","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.000039235892,0.0000045822544,0.00013025245,0.000095922216,0.000021121694,0.00052726344,0.000027726239,0.000039087623,0.000052464035,0.0005783179,0.99566674,0.0028171514],"study_design_scores_gemma":[0.00022806435,0.000030647076,0.0017428015,0.00061645004,0.00015360072,0.003007356,0.00015980769,0.0005286966,0.00067386025,0.0040556276,0.9887227,0.00008051192],"about_ca_topic_score_codex":0.01881538,"about_ca_topic_score_gemma":0.02630724,"teacher_disagreement_score":0.08696977,"about_ca_system_score_codex":0.003091618,"about_ca_system_score_gemma":0.005608797,"threshold_uncertainty_score":0.29094285},"labels":[],"label_agreement":null},{"id":"W4395074959","doi":"10.1038/s41588-024-01726-6","title":"Joint genotypic and phenotypic outcome modeling improves base editing variant effect quantification","year":2024,"lang":"en","type":"article","venue":"Nature Genetics","topic":"CRISPR and Genetic Engineering","field":"Biochemistry, Genetics and Molecular Biology","cited_by":33,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Université de Montréal; Montreal Heart Institute","funders":"National Human Genome Research Institute; National Heart, Lung, and Blood Institute; National Health and Medical Research Council; State Government of Victoria; National Organization for Rare Disorders; National Institute of Environmental Health Sciences; American Cancer Society; National Institute of General Medical Sciences; Medical Research Council; American Heart Association; U.S. Department of Health and Human Services","keywords":"Biology; Computational biology; Genome editing; Phenotype; Genetics; Bayes' theorem; Cas9; Gene; CRISPR; Computer science; Bayesian probability; Artificial intelligence","score_opus":0.010012102327567163,"score_gpt":0.29328591061632714,"score_spread":0.28327380828876,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4395074959","genre_codex":"methods","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":null,"domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.12543735,0.0001059751,0.8694378,0.00014600331,0.00003351923,0.000039423918,0.0006323849,0.0018592854,0.0023082593],"genre_scores_gemma":[0.9181353,0.0000909785,0.07915359,0.000079202706,0.000012491334,0.000058851165,0.0006688234,0.00031813607,0.00148274],"study_design_codex":"simulation_or_modeling","study_design_gemma":"simulation_or_modeling","domain_scores_codex":[0.99906546,0.00028930372,0.000057238474,0.0002653805,0.00026074715,0.000061873485],"domain_scores_gemma":[0.99745756,0.0015985791,0.00027968702,0.00041116582,0.00019382872,0.00005919328],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0021380556,0.0008942697,0.0006537943,0.0005505313,0.00018245114,0.0010566884,0.0008121568,0.0006628244,0.0011400833],"category_scores_gemma":[0.0057432037,0.00026588325,0.0007727654,0.0004727681,0.0003821474,0.00068637123,0.00075942045,0.00072373834,0.0002462373],"study_design_candidate":"simulation_or_modeling","study_design_consensus":"simulation_or_modeling","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0002630126,0.00015025919,0.014049503,0.00009126623,0.00019711757,0.0003062398,0.000052499432,0.8704319,0.026346413,0.013174036,0.0007717347,0.0741661],"study_design_scores_gemma":[0.000007315285,0.000044470376,0.0013613912,0.0000048506813,0.00004179992,0.00007155957,0.000005667059,0.98356724,0.007938498,0.0065607545,0.00038427956,0.000012095353],"about_ca_topic_score_codex":0.0022562654,"about_ca_topic_score_gemma":0.0035160466,"teacher_disagreement_score":0.0022562654,"about_ca_system_score_codex":0.00044936,"about_ca_system_score_gemma":0.00073763874,"threshold_uncertainty_score":0.0113072395},"labels":[],"label_agreement":null},{"id":"W4395667837","doi":"10.1038/s41588-024-01725-7","title":"Multi-ancestry genome-wide association study of kidney cancer identifies 63 susceptibility regions","year":2024,"lang":"en","type":"review","venue":"Nature Genetics","topic":"Genetic Associations and Epidemiology","field":"Biochemistry, Genetics and Molecular Biology","cited_by":48,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Ontario Institute for Cancer Research; Princess Margaret Cancer Centre; University Health Network","funders":"Medical Research Council; National Institutes of Health; World Health Organization","keywords":"Biology; Kidney cancer; Genome-wide association study; Odds ratio; Locus (genetics); Expression quantitative trait loci; Quantitative trait locus; Genetics; Single-nucleotide polymorphism; Genetic association; Cancer; Genetic architecture; Kidney disease; Gene; Genotype; Internal medicine; Medicine; Endocrinology","score_opus":0.04368814229223789,"score_gpt":0.3799506151065461,"score_spread":0.3362624728143082,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4395667837","genre_codex":"review","genre_gemma":"review","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"review","genre_consensus":"review","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.00011295805,0.997934,0.00027932733,0.00084330654,0.0002299576,0.0000040915866,0.000073438045,0.00000976235,0.0005132193],"genre_scores_gemma":[0.0006625836,0.99756,0.00039117216,0.0004806982,0.00038794652,0.000008029523,0.00011171064,0.000002198642,0.00039548904],"study_design_codex":"design_other","study_design_gemma":"observational","domain_scores_codex":[0.99954873,0.00011265407,0.000060762977,0.00009645457,0.00014552599,0.00003591891],"domain_scores_gemma":[0.99845886,0.0009808918,0.00013405868,0.00004240694,0.00027790063,0.00010590594],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0020200412,0.0011045755,0.002019257,0.0022722883,0.00023153913,0.001204049,0.0015337507,0.001710633,0.0025238886],"category_scores_gemma":[0.0023211506,0.00038908457,0.00080568425,0.0032787588,0.00055524014,0.00082217477,0.00094153715,0.0020759976,0.0015036195],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00019246856,0.00004577785,0.0015441844,0.006802295,0.0005338289,0.00021530576,0.000024998437,0.0002392032,0.00066638057,0.0026157945,0.04168169,0.945438],"study_design_scores_gemma":[0.00013250049,0.00013134518,0.012341563,0.007826044,0.0014335734,0.0017650953,0.0000740696,0.00020659615,0.0005842141,0.0060851783,0.96935016,0.00006970749],"about_ca_topic_score_codex":0.0035499595,"about_ca_topic_score_gemma":0.0068465853,"teacher_disagreement_score":0.0035499595,"about_ca_system_score_codex":0.0007369491,"about_ca_system_score_gemma":0.0019845369,"threshold_uncertainty_score":0.010683179},"labels":[],"label_agreement":null},{"id":"W4396531762","doi":"10.1038/s41588-024-01714-w","title":"Genome-wide analysis in over 1 million individuals of European ancestry yields improved polygenic risk scores for blood pressure traits","year":2024,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Genetic Associations and Epidemiology","field":"Biochemistry, Genetics and Molecular Biology","cited_by":182,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Centre for Global Health Research; McMaster University; Population Health Research Institute","funders":"National Institute of Diabetes and Digestive and Kidney Diseases; National Heart, Lung, and Blood Institute; National Institute on Aging; Medical Research Council; School of Medicine, Duke University; National Institutes of Health; Isfahan University of Medical Sciences; Brigham and Women's Hospital; British Heart Foundation; Eesti Teadusagentuur; Novo Nordisk Fonden; Israel Science Foundation; University of Oxford; King's College London; Department of Health and Social Care; U.S. Department of Veterans Affairs; National Institute of Neurological Disorders and Stroke; National Institute for Health and Care Research","keywords":"Biology; Polygenic risk score; Multifactorial Inheritance; Genome-wide association study; Quantitative trait locus; Genetics; Blood pressure; Genome; Evolutionary biology; Gene; Single-nucleotide polymorphism; Genotype","score_opus":0.00920210464408175,"score_gpt":0.26849083059599926,"score_spread":0.2592887259519175,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4396531762","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.98744863,0.0006161174,0.0059056524,0.0002638389,0.000035656623,0.000019358864,0.0045995107,0.00013300059,0.0009782404],"genre_scores_gemma":[0.99217707,0.00019130418,0.002437123,0.00013035875,0.00004259412,0.000023258393,0.00465033,0.00002940459,0.00031849495],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9982809,0.00073380425,0.000119758726,0.0005673091,0.0001774848,0.00012092048],"domain_scores_gemma":[0.9972792,0.0012488865,0.00048296832,0.0005805696,0.00022077418,0.00018768676],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0024322118,0.00057787687,0.0006831028,0.00072221225,0.0005642341,0.0008893454,0.00029344417,0.00044551666,0.0031821947],"category_scores_gemma":[0.005080948,0.00018260516,0.0011894131,0.0015100783,0.0002802377,0.00025496678,0.0007240139,0.00064062123,0.00055449706],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0012203931,0.00014090653,0.9489965,0.00010472104,0.002389062,0.00035317848,0.00015086071,0.0010678663,0.019002162,0.00018962006,0.0020834997,0.024301246],"study_design_scores_gemma":[0.000063564294,0.00013147836,0.9936935,0.000017430606,0.00046126868,0.0005788257,0.000065058644,0.0018650852,0.0013345825,0.0003619859,0.0014139287,0.000013433511],"about_ca_topic_score_codex":0.0022365905,"about_ca_topic_score_gemma":0.0031884736,"teacher_disagreement_score":0.0031821947,"about_ca_system_score_codex":0.00012648206,"about_ca_system_score_gemma":0.00020331371,"threshold_uncertainty_score":0.012862921},"labels":[],"label_agreement":null},{"id":"W4396553809","doi":"10.1038/s41588-024-01737-3","title":"Genomes of multicellular algal sisters to land plants illuminate signaling network evolution","year":2024,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Protist diversity and phylogeny","field":"Biochemistry, Genetics and Molecular Biology","cited_by":97,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Dalhousie University","funders":"National Institute of General Medical Sciences; Deutsche Forschungsgemeinschaft; U.S. Department of Agriculture; National Institute of Allergy and Infectious Diseases; LABoratoires d’EXcellence ARCANE; Bill and Melinda Gates Foundation; Foundation for the National Institutes of Health","keywords":"Biology; Multicellular organism; Gene; Genome; Most recent common ancestor; Evolutionary biology; Plant evolution; Genetics; Ecology","score_opus":0.006103680268823983,"score_gpt":0.22627338501022448,"score_spread":0.2201697047414005,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4396553809","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99077624,0.00116549,0.0041009584,0.00013892275,0.000015480897,0.0000050061553,0.0016565395,0.00015188138,0.001989543],"genre_scores_gemma":[0.99001175,0.0007170813,0.005025891,0.00009127636,0.000009355535,0.000007566711,0.0030412357,0.00006749593,0.0010284056],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.99989057,0.00001021727,0.0000047186877,0.000051951254,0.000024613726,0.000017940643],"domain_scores_gemma":[0.99966884,0.00011109648,0.00008119826,0.00004842761,0.000033779783,0.000056756442],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00019054263,0.00025009064,0.00023709846,0.0006860639,0.00061627076,0.00057106174,0.00020969208,0.00037452026,0.0014712533],"category_scores_gemma":[0.0005769207,0.00020403888,0.00020692714,0.00083743257,0.00024399027,0.00064914953,0.0007424102,0.00046978926,0.00031678827],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00043469487,0.000033460536,0.09455562,0.0003299938,0.00013065408,0.00042813396,0.0010574611,0.0019544936,0.85939723,0.0036117036,0.00070854265,0.037358064],"study_design_scores_gemma":[0.000039465034,0.00017252141,0.86101806,0.0001274444,0.00019855256,0.0012590803,0.0014572752,0.011477715,0.073465474,0.006965216,0.043759223,0.000060018978],"about_ca_topic_score_codex":0.0017744125,"about_ca_topic_score_gemma":0.004745184,"teacher_disagreement_score":0.0017744125,"about_ca_system_score_codex":0.00038071928,"about_ca_system_score_gemma":0.00027452924,"threshold_uncertainty_score":0.0049218535},"labels":[],"label_agreement":null},{"id":"W4396695995","doi":"10.1038/s41588-024-01717-7","title":"STR mutations on chromosome 15q cause thyrotropin resistance by activating a primate-specific enhancer of MIR7-2/MIR1179","year":2024,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Genomics and Chromatin Dynamics","field":"Biochemistry, Genetics and Molecular Biology","cited_by":24,"is_retracted":false,"has_abstract":false,"route_ca_aff":false,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"","funders":"National Institute of Diabetes and Digestive and Kidney Diseases; National Human Genome Research Institute; University of Illinois at Urbana-Champaign; University of Washington; Université de Montréal; Centre hospitalier régional universitaire de Lille; Primate Research Institute, Kyoto University; National Institutes of Health; Johns Hopkins University","keywords":"Biology; Locus (genetics); Genetics; Enhancer; Chromosome; Regulator; Chromosome 15; Gene; Transcription factor","score_opus":0.005977203835920668,"score_gpt":0.26078500344778605,"score_spread":0.2548077996118654,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4396695995","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99182874,0.00027116184,0.0036431858,0.00025518204,0.000096040785,0.00004416357,0.0005942977,0.0003375764,0.0029297478],"genre_scores_gemma":[0.99646145,0.000099112534,0.0013411564,0.00011608213,0.000025842775,0.000016355714,0.0002826433,0.00007779447,0.0015795239],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9997143,0.000048168225,0.000033028373,0.00006490242,0.000105005005,0.000034577937],"domain_scores_gemma":[0.9995515,0.0001412442,0.0001957243,0.000022951275,0.000012599959,0.000075930824],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00021246658,0.0008755945,0.00028332448,0.0008199398,0.000373124,0.00030643467,0.00055113115,0.0009661332,0.004937917],"category_scores_gemma":[0.00046320766,0.00033129187,0.00061676634,0.00042822823,0.000750181,0.00014037862,0.0006794277,0.0007069501,0.0011306889],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00035331916,0.000055159937,0.0048054843,0.00005277955,0.0001093089,0.015309192,0.00016786093,0.0004215166,0.9720728,0.0011451881,0.000497606,0.005009913],"study_design_scores_gemma":[0.0008127898,0.0014668865,0.15578204,0.000100876394,0.00058539025,0.12703076,0.0005998482,0.013798641,0.67110443,0.0037901,0.024752555,0.0001757156],"about_ca_topic_score_codex":0.000770004,"about_ca_topic_score_gemma":0.0014879466,"teacher_disagreement_score":0.004937917,"about_ca_system_score_codex":0.0003199824,"about_ca_system_score_gemma":0.00021758759,"threshold_uncertainty_score":0.01651895},"labels":[],"label_agreement":null},{"id":"W4396863977","doi":"10.1038/s41588-024-01732-8","title":"Genetic mapping across autoimmune diseases reveals shared associations and mechanisms","year":2024,"lang":"en","type":"article","venue":"Nature Genetics","topic":"T-cell and B-cell Immunology","field":"Immunology and Microbiology","cited_by":34,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Toronto; St. Michael's Hospital","funders":"National Institute of Neurological Disorders and Stroke; National Institute of Allergy and Infectious Diseases; National Institute of General Medical Sciences; Weill Institute for Neurosciences, University of California, San Francisco; National Institute of Mental Health; Irving Medical Center, Columbia University; University of California, San Francisco; University of Oxford; National Multiple Sclerosis Society; Genentech; Menzies Institute for Medical Research; Università degli Studi del Piemonte Orientale; Oklahoma Medical Research Foundation; Karolinska Institutet; Deutsche Forschungsgemeinschaft; National Human Genome Research Institute; Nederlandse Organisatie voor Wetenschappelijk Onderzoek; Wellcome Trust; Rijksuniversiteit Groningen; University of Tasmania; National Institute of Child Health and Human Development; National Institute of Arthritis and Musculoskeletal and Skin Diseases; National Institute of Diabetes and Digestive and Kidney Diseases; Lupus Research Alliance; Harvard NeuroDiscovery Center; U.S. Department of Health and Human Services; Case Western Reserve University; Università degli Studi di Milano","keywords":"Biology; Allele; Genetics; Quantitative trait locus; Mechanism (biology); Computational biology; Genome-wide association study; Evolutionary biology; Gene; Genotype; Single-nucleotide polymorphism","score_opus":0.010009162402446915,"score_gpt":0.2524728926602532,"score_spread":0.24246373025780626,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4396863977","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9919457,0.0020710663,0.004203261,0.00027657504,0.000043452415,0.000012218562,0.000179425,0.00006984601,0.0011985338],"genre_scores_gemma":[0.9963355,0.001029191,0.001703549,0.00016057487,0.000072990144,0.000012602493,0.00018507964,0.000021501444,0.00047901488],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9990062,0.00022258091,0.00009949205,0.0003524248,0.00019129281,0.000128072],"domain_scores_gemma":[0.9989065,0.0003463427,0.00038508716,0.00015393991,0.00006595797,0.00014209485],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00070259743,0.0008744256,0.00075579155,0.002154155,0.00039544847,0.00090017606,0.000846135,0.0009119931,0.0017532728],"category_scores_gemma":[0.0010088332,0.00044925034,0.00064382027,0.0010836197,0.0010323967,0.0005791318,0.0013619206,0.00097220525,0.00026169533],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.002188296,0.00023013979,0.14227535,0.0003467588,0.0011666715,0.0058018505,0.0006076762,0.00087662064,0.8057639,0.007754758,0.00047464203,0.032513306],"study_design_scores_gemma":[0.00037031423,0.00063064793,0.9006167,0.00020823859,0.001871429,0.018689308,0.0007579418,0.002937667,0.05556511,0.01326856,0.0049806787,0.00010327549],"about_ca_topic_score_codex":0.00044370396,"about_ca_topic_score_gemma":0.00036928465,"teacher_disagreement_score":0.002154155,"about_ca_system_score_codex":0.00021417734,"about_ca_system_score_gemma":0.00022293207,"threshold_uncertainty_score":0.005865276},"labels":[],"label_agreement":null},{"id":"W4399300066","doi":"10.1038/s41588-024-01771-1","title":"Improved functional mapping of complex trait heritability with GSA-MiXeR implicates biologically specific gene sets","year":2024,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Genetic Associations and Epidemiology","field":"Biochemistry, Genetics and Molecular Biology","cited_by":31,"is_retracted":false,"has_abstract":false,"route_ca_aff":false,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"","funders":"David Geffen School of Medicine, University of California, Los Angeles; Universidad de Granada; NIH Clinical Center; National Heart, Lung, and Blood Institute; National Institute on Aging; Sorbonne Université; State University of New York Upstate Medical University; Servicio Gallego de Salud; University of Sydney; National Institute of Mental Health; Helse Sør-Øst RHF; Medical Research Council; NIHR Maudsley Biomedical Research Centre; Centro de Investigación Biomédica en Red de Salud Mental; Department of Psychology, Harvard University; Institute of Psychiatry, Psychology and Neuroscience, King’s College London; Veterans Affairs San Diego Healthcare System; National Taiwan University Hospital; University of California, Los Angeles; University of South Australia; Graduate School of Frontier Sciences, University of Tokyo; Hebrew University of Jerusalem; Université de Paris; Institut National de la Santé et de la Recherche Médicale; Sun Yat-sen University; Humboldt-Universität zu Berlin; H. Lundbeck A/S; Nasjonalforeningen for Folkehelsen; University of Chinese Academy of Sciences; Centre d'Imagerie BioMédicale; Stony Brook University; Pomorski Uniwersytet Medyczny W Szczecinie; Rheinische Friedrich-Wilhelms-Universität Bonn; Massachusetts General Hospital; University of Colorado Boulder; Universitas Indonesia; University of California, San Diego; Universitetet i Oslo; National and Kapodistrian University of Athens; Universitetet i Bergen; H2020 Marie Skłodowska-Curie Actions; McGill University; Samfundet Folkhälsan; Terveyden ja hyvinvoinnin laitos; Universitat de Barcelona; King's College London; Centre National de la Recherche Scientifique; Medizinische Universität Wien; Euskal Herriko Unibertsitatea; Department of Psychiatry, Columbia University; Universität Wien; Helsingin Yliopisto; Chonnam National University; University of Nicosia; South Australian Health and Medical Research Institute; Universitair Medisch Centrum Utrecht; Chinese Academy of Sciences; Statens Serum Institut; Janssen Research and Development; RIKEN; Universität Heidelberg; Universiteit van Amsterdam; Norges Forskningsråd; University of Leicester; Université de Rouen; National Taiwan University; South London and Maudsley NHS Foundation Trust; University of Tokyo; National University of Singapore; NorthShore University HealthSystem; European Commission; Institute of Genetics; Broad Institute; National Institute on Drug Abuse; Monash University; VA Greater Los Angeles Healthcare System; University College Cork; Sunovion; University of New South Wales; Universiteit Maastricht; F. Hoffmann-La Roche; Euroscience; National Institutes of Health; Syracuse University; University of Melbourne; University of North Carolina at Chapel Hill; Harvard University; University of Pennsylvania; National Research Centre; Philipps-Universität Marburg; University of Chicago; Horizon 2020 Framework Programme; Région Normandie; Fujita Health University; Universiteit Utrecht; Universidad de Oviedo; Universität Basel; National Institute for Health and Care Research; State University of New York; Virginia Commonwealth University; Yale University","keywords":"Biology; Linkage disequilibrium; Heritability; Computational biology; Genetics; Gene; Quantitative trait locus; Genome-wide association study; Genetic association; Trait; Gene regulatory network; Allele; Single-nucleotide polymorphism; Haplotype; Gene expression; Genotype; Computer science","score_opus":0.024371764360754535,"score_gpt":0.26649326803606327,"score_spread":0.24212150367530874,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4399300066","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.82119113,0.00050983246,0.17005128,0.0003775782,0.0001132511,0.00015106102,0.002327086,0.0012016289,0.004077038],"genre_scores_gemma":[0.92599475,0.000282634,0.068656884,0.00018148431,0.00005223269,0.00017503346,0.0017007025,0.00040885972,0.0025474448],"study_design_codex":"bench_or_experimental","study_design_gemma":"simulation_or_modeling","domain_scores_codex":[0.99850935,0.0004539505,0.000094615054,0.00059601077,0.00019305667,0.00015300685],"domain_scores_gemma":[0.99724895,0.0017784232,0.000316176,0.0003837454,0.00006820871,0.00020441618],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0020341694,0.0012237133,0.0011745935,0.0030156863,0.0007286737,0.00094842387,0.0011595025,0.0007725883,0.0067682187],"category_scores_gemma":[0.0020756084,0.0007321903,0.0016455246,0.0012369391,0.0010114724,0.00043837915,0.0016093381,0.0019663058,0.0007166738],"study_design_candidate":"simulation_or_modeling","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00078851776,0.00020728691,0.007973668,0.00008614666,0.00016332773,0.00026755937,0.0001331817,0.0013104747,0.9679757,0.0049997065,0.00017180231,0.015922716],"study_design_scores_gemma":[0.0006125454,0.0008351589,0.19534184,0.000088263245,0.0007981825,0.0026911264,0.00013966786,0.034758125,0.7448478,0.009889344,0.00979852,0.00019950692],"about_ca_topic_score_codex":0.0013316339,"about_ca_topic_score_gemma":0.0029524332,"teacher_disagreement_score":0.0067682187,"about_ca_system_score_codex":0.00049332844,"about_ca_system_score_gemma":0.00039536992,"threshold_uncertainty_score":0.022641957},"labels":[],"label_agreement":null},{"id":"W4399359365","doi":"10.1038/s41588-024-01763-1","title":"Genome-wide meta-analyses of restless legs syndrome yield insights into genetic architecture, disease biology and risk prediction","year":2024,"lang":"en","type":"review","venue":"Nature Genetics","topic":"Restless Legs Syndrome Research","field":"Medicine","cited_by":52,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Canadian Heart Research Centre; University of Ottawa; Université de Montréal; Hôpital du Sacré-Cœur de Montréal; McGill University; Canadian Sleep & Circadian Network; Montreal Neurological Institute and Hospital","funders":"NIHR Cambridge Biomedical Research Centre; Leibniz-Gemeinschaft; Science and Technology Facilities Council; Economic and Social Research Council; Natural Sciences and Engineering Research Council of Canada; Canadian Institutes of Health Research; NIHR BioResource; Danmarks Frie Forskningsfond; Dell EMC; Deutsche Forschungsgemeinschaft; Health and Social Care Research and Development Division; Novo Nordisk; Public Health Agency; Engineering and Physical Sciences Research Council; University of Thessaly; European Commission; Medical Research Council; Department of Health and Social Care; European Regional Development Fund; Bundesministerium für Bildung und Forschung; National Institute on Aging; NHS Blood and Transplant; National Institute for Health and Care Research; Heart and Stroke Foundation of Canada; Novo Nordisk Fonden; National Institute of Neurological Disorders and Stroke; British Heart Foundation; University of Cambridge; Wellcome Trust; Cancer Research UK; Helmholtz Zentrum München; Westfälische Wilhelms-Universität Münster; Emory University; Chief Scientist Office, Scottish Government Health and Social Care Directorate; Scottish Government; National Institutes of Health; Univerzita Karlova v Praze; Restless Legs Syndrome Foundation","keywords":"Biology; Mendelian randomization; Genome-wide association study; Genetic architecture; Disease; Locus (genetics); Genetics; 1000 Genomes Project; Drug repositioning; Restless legs syndrome; Epistasis; Bioinformatics; Computational biology; Gene; Quantitative trait locus; Drug; Internal medicine; Genotype; Single-nucleotide polymorphism; Genetic variants; Medicine; Neuroscience","score_opus":0.11262341933308051,"score_gpt":0.42168514586926437,"score_spread":0.30906172653618386,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4399359365","genre_codex":"review","genre_gemma":"review","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"review","genre_consensus":"review","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.0009657171,0.9978344,0.00040320243,0.00032616657,0.00008336048,0.000009760025,0.00020931535,0.000012263711,0.00015590982],"genre_scores_gemma":[0.037821256,0.95907444,0.0014646482,0.0005293282,0.0002462748,0.000047977428,0.00060634664,0.000015221197,0.00019448063],"study_design_codex":"design_other","study_design_gemma":"meta_analysis","domain_scores_codex":[0.9978551,0.0011796415,0.00028236784,0.00033766447,0.00025346267,0.00009162421],"domain_scores_gemma":[0.9917693,0.0069890367,0.0005269937,0.0002202679,0.00040550262,0.00008895538],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.006223666,0.0018971087,0.006263331,0.0033662175,0.00019929331,0.0015590992,0.0011803573,0.0012727452,0.0028831584],"category_scores_gemma":[0.010619845,0.0005796675,0.0098688435,0.0037531683,0.00030940908,0.00072710984,0.0008352367,0.0015499014,0.0003569014],"study_design_candidate":"meta_analysis","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0024455378,0.00007764309,0.016930927,0.20146386,0.29829866,0.00038728028,0.00010043711,0.0044694985,0.0013477994,0.0024361266,0.011121353,0.46092087],"study_design_scores_gemma":[0.0011757349,0.00083537714,0.06821694,0.07142842,0.7343304,0.0013423864,0.00018520153,0.0042609735,0.0016555223,0.013882329,0.10249327,0.00019342524],"about_ca_topic_score_codex":0.0030051344,"about_ca_topic_score_gemma":0.0055895727,"teacher_disagreement_score":0.006263331,"about_ca_system_score_codex":0.0009104472,"about_ca_system_score_gemma":0.0015818056,"threshold_uncertainty_score":0.03291428},"labels":[],"label_agreement":null},{"id":"W4399641977","doi":"10.1038/s41588-024-01793-9","title":"Synthetic surrogates improve power for genome-wide association studies of partially missing phenotypes in population biobanks","year":2024,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Genetic Associations and Epidemiology","field":"Biochemistry, Genetics and Molecular Biology","cited_by":15,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Toronto","funders":"National Human Genome Research Institute; National Heart, Lung, and Blood Institute; Natural Sciences and Engineering Research Council of Canada; National Cancer Institute; U.S. Department of Health and Human Services; National Institutes of Health; Canadian Network for Research and Innovation in Machining Technology, Natural Sciences and Engineering Research Council of Canada","keywords":"Biobank; Imputation (statistics); Genome-wide association study; Missing data; Genetic association; Spurious relationship; Statistical power; Population; Trait; Biology; Data mining; Computational biology; Computer science; Statistics; Genetics; Machine learning; Single-nucleotide polymorphism; Mathematics; Genotype; Gene; Medicine","score_opus":0.011982570315027865,"score_gpt":0.29975235805414385,"score_spread":0.287769787739116,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4399641977","genre_codex":"methods","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":null,"domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.18819566,0.0018484888,0.7992921,0.002861602,0.00052088004,0.00022417701,0.0033638307,0.0013987527,0.002294548],"genre_scores_gemma":[0.86204684,0.00050286215,0.12869693,0.0013167245,0.00031456174,0.00042520397,0.005179378,0.00028395758,0.0012335571],"study_design_codex":"simulation_or_modeling","study_design_gemma":"simulation_or_modeling","domain_scores_codex":[0.9236592,0.06705226,0.0019845099,0.004628121,0.0020794969,0.0005964726],"domain_scores_gemma":[0.60093504,0.35761294,0.008518405,0.02781079,0.003396369,0.0017264081],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.10753805,0.0012146969,0.0028973345,0.001892677,0.0012904168,0.004017352,0.0030555413,0.0032846234,0.004824389],"category_scores_gemma":[0.28970146,0.0014704277,0.0024831542,0.0028201083,0.003128387,0.0038676048,0.0056972597,0.003926248,0.0010027856],"study_design_candidate":"simulation_or_modeling","study_design_consensus":"simulation_or_modeling","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.017473632,0.001119564,0.23997267,0.0019331101,0.00772842,0.0023730393,0.0015795764,0.31152022,0.008319146,0.15416923,0.016381957,0.2374294],"study_design_scores_gemma":[0.0018245814,0.0011283635,0.019926986,0.00026312564,0.0012183863,0.0012732586,0.00022990523,0.6293952,0.002852668,0.33418095,0.007564372,0.00014222998],"about_ca_topic_score_codex":0.0007835425,"about_ca_topic_score_gemma":0.00082102546,"teacher_disagreement_score":0.10753805,"about_ca_system_score_codex":0.00053122453,"about_ca_system_score_gemma":0.0015882961,"threshold_uncertainty_score":0.56872237},"labels":[],"label_agreement":null},{"id":"W4399977123","doi":"10.1038/s41588-024-01786-8","title":"A proposal for an inclusive working definition of genetic discrimination to promote a more coherent debate","year":2024,"lang":"en","type":"review","venue":"Nature Genetics","topic":"Biomedical Ethics and Regulation","field":"Medicine","cited_by":6,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"McGill Genome Centre; University of Toronto; Université de Montréal; St. Michael's Hospital; McGill University","funders":"","keywords":"Genetic discrimination; Phenomenon; Context (archaeology); Perspective (graphical); Equity (law); Face (sociological concept); Dignity; Social equality; Sociology; Epistemology; Biology; Genetic testing; Political science; Social science; Genetics; Law; Computer science","score_opus":0.06333586202631902,"score_gpt":0.4013198722210346,"score_spread":0.3379840101947156,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4399977123","genre_codex":"commentary","genre_gemma":"review","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"review","genre_consensus":null,"domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.0005416631,0.2459242,0.03580009,0.6515862,0.036352545,0.0001439537,0.00013455315,0.00012901712,0.029387806],"genre_scores_gemma":[0.034478787,0.13008206,0.07795679,0.7139092,0.022702921,0.001596669,0.00029946625,0.00020307838,0.018771136],"study_design_codex":"theoretical_or_conceptual","study_design_gemma":"theoretical_or_conceptual","domain_scores_codex":[0.97190905,0.01655074,0.0022756066,0.0022791664,0.0058682486,0.0011172685],"domain_scores_gemma":[0.9691817,0.023546593,0.001285038,0.0014184004,0.0035051252,0.0010632086],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.048859928,0.0016054224,0.0038612778,0.005999559,0.003255357,0.010465372,0.0058761165,0.036044672,0.004403657],"category_scores_gemma":[0.043356106,0.00093829527,0.002524495,0.004165289,0.034534786,0.02035595,0.00879359,0.044603713,0.0019005582],"study_design_candidate":"theoretical_or_conceptual","study_design_consensus":"theoretical_or_conceptual","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.000014404951,0.000023791685,0.00002688249,0.0009938297,0.000028212104,0.000085857995,0.0006073424,0.00011992951,0.00013413905,0.9336551,0.041464977,0.022845482],"study_design_scores_gemma":[0.000055324505,0.00002213887,0.000117781274,0.004193606,0.000053729233,0.0002507671,0.0004055978,0.00015483386,0.00011387309,0.5366984,0.4578891,0.000044872853],"about_ca_topic_score_codex":0.002992782,"about_ca_topic_score_gemma":0.0042214426,"teacher_disagreement_score":0.048859928,"about_ca_system_score_codex":0.008495921,"about_ca_system_score_gemma":0.024013769,"threshold_uncertainty_score":0.25839907},"labels":[],"label_agreement":null},{"id":"W4400091307","doi":"10.1038/s41588-024-01808-5","title":"A common flanking variant is associated with enhanced stability of the FGF14-SCA27B repeat locus","year":2024,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Fibroblast Growth Factor Research","field":"Biochemistry, Genetics and Molecular Biology","cited_by":34,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Hospital for Sick Children; SickKids Foundation; Montreal Neurological Institute and Hospital; University of Toronto; Children's Hospital of Eastern Ontario; McGill University; University of Ottawa","funders":"National Institute of Neurological Disorders and Stroke; National Cancer Institute; National Institute on Drug Abuse; UCLH Biomedical Research Centre; National Health and Medical Research Council; Medical Research Council; University College London Hospitals NHS Foundation Trust; Government of Canada; Deutsche Forschungsgemeinschaft; Génome Québec; Ontario Genomics Institute; Canadian Institutes of Health Research; Genome Canada; U.S. Department of Health and Human Services; National Institutes of Health; Ontario Genomics; National Center for Advancing Translational Sciences; National Human Genome Research Institute; Wellcome Trust","keywords":"Biology; Locus (genetics); Genetics; Computational biology; Gene","score_opus":0.008254799315850726,"score_gpt":0.2659610445469234,"score_spread":0.25770624523107266,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4400091307","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9945205,0.00025993653,0.0027505192,0.00011994488,0.000054164753,0.0000348403,0.0007292693,0.0001316307,0.0013993088],"genre_scores_gemma":[0.99729365,0.00005804659,0.0010079346,0.000052039573,0.000039126076,0.0000130565795,0.00042804077,0.00004764493,0.001060337],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.99943393,0.00007127477,0.00008271055,0.00020767031,0.00012672739,0.00007766558],"domain_scores_gemma":[0.9985998,0.00032032473,0.00052126695,0.00013700778,0.00012420806,0.00029736635],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00023170144,0.0010727365,0.00061887474,0.0017123928,0.00074620603,0.0003728166,0.0008543758,0.0013215799,0.0077076945],"category_scores_gemma":[0.0011081119,0.00024266417,0.0008282697,0.0011200444,0.00068400643,0.00020097906,0.00064261723,0.0007919231,0.0012213878],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.003235633,0.00034337133,0.047902085,0.0001520322,0.000761397,0.073488705,0.00041974356,0.00059291546,0.857145,0.0015575604,0.0010911913,0.013310329],"study_design_scores_gemma":[0.00041079335,0.0013276053,0.5694085,0.00008990444,0.0009611388,0.29515052,0.0003571699,0.0036929734,0.119356565,0.0019068281,0.0071379063,0.00020001299],"about_ca_topic_score_codex":0.0028661406,"about_ca_topic_score_gemma":0.0034355167,"teacher_disagreement_score":0.0077076945,"about_ca_system_score_codex":0.0002586083,"about_ca_system_score_gemma":0.00034133554,"threshold_uncertainty_score":0.02578479},"labels":[],"label_agreement":null},{"id":"W4400208202","doi":"10.1038/s41588-024-01798-4","title":"Understanding the genetic complexity of puberty timing across the allele frequency spectrum","year":2024,"lang":"en","type":"article","venue":"Nature Genetics","topic":"RNA Research and Splicing","field":"Biochemistry, Genetics and Molecular Biology","cited_by":49,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Centre Hospitalier Universitaire Sainte-Justine; Centre for Global Health Research; University of Toronto; Mount Sinai Hospital; Lunenfeld-Tanenbaum Research Institute; Université de Montréal","funders":"National Cancer Institute; Medical Research Foundation; Medical Research Council; Research Councils UK; Novo Nordisk Fonden; National Institute of Environmental Health Sciences","keywords":"Biology; Allele; Allele frequency; Genetics; Evolutionary biology; Gene","score_opus":0.06314701979262892,"score_gpt":0.33085405900025744,"score_spread":0.2677070392076285,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4400208202","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99441284,0.00086647406,0.003097558,0.00025410877,0.000011724684,0.000007042271,0.0005414895,0.000027902146,0.0007808588],"genre_scores_gemma":[0.99764806,0.00040599259,0.0012840831,0.00007027856,0.00002129561,0.000006474621,0.0002707229,0.000014840539,0.00027827325],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9995048,0.00013161062,0.000028653441,0.00021062531,0.00006203769,0.00006223686],"domain_scores_gemma":[0.99918705,0.00037645965,0.00025447184,0.00009443624,0.00003646829,0.000051208444],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00061032205,0.00028957275,0.00028597424,0.00093268574,0.0002100767,0.0005923073,0.00023720585,0.00037853126,0.001672575],"category_scores_gemma":[0.002132145,0.00016639952,0.00031468057,0.00071050343,0.00032180114,0.00032402473,0.0005074982,0.0004849935,0.00012790448],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00031960488,0.00004661637,0.91860396,0.00006423612,0.0006823838,0.0006757623,0.00053670694,0.0011013395,0.04321806,0.0014947813,0.00047113624,0.03278547],"study_design_scores_gemma":[0.000009027045,0.000058324662,0.9939412,0.000013914945,0.000112524125,0.0007791342,0.00011880361,0.0013881994,0.0010472541,0.0012771568,0.001245373,0.000009043254],"about_ca_topic_score_codex":0.0026167925,"about_ca_topic_score_gemma":0.0034999696,"teacher_disagreement_score":0.0026167925,"about_ca_system_score_codex":0.00011903074,"about_ca_system_score_gemma":0.0001623494,"threshold_uncertainty_score":0.005595267},"labels":[],"label_agreement":null},{"id":"W4400362568","doi":"10.1038/s41588-024-01800-z","title":"Saturation genome editing maps the functional spectrum of pathogenic VHL alleles","year":2024,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Epigenetics and DNA Methylation","field":"Biochemistry, Genetics and Molecular Biology","cited_by":48,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Toronto; Hospital for Sick Children","funders":"Medical Research Council; Deutsche Forschungsgemeinschaft; Francis Crick Institute; Cancer Research UK; Wellcome Trust","keywords":"Biology; Genetics; Gene; Single-nucleotide polymorphism; Germline; Phenotype; Allele; Computational biology; Genome; Functional genomics; Genotype; Genomics","score_opus":0.007284651883165979,"score_gpt":0.23762400290638724,"score_spread":0.23033935102322126,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4400362568","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9042239,0.00064993434,0.08687213,0.0002163934,0.00003300264,0.00011400607,0.001964422,0.0011724498,0.004753763],"genre_scores_gemma":[0.97116345,0.0003930523,0.025705904,0.00012288074,0.000007798811,0.00006101648,0.000983814,0.0002349952,0.0013272432],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9995153,0.00007964643,0.000026200209,0.00015639004,0.00016355545,0.000058904112],"domain_scores_gemma":[0.99918133,0.0003831948,0.00018926332,0.00014311298,0.00005879633,0.000044295455],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00057449314,0.0004575455,0.00038759896,0.0010255646,0.00028211312,0.00051450497,0.00036685087,0.0004909215,0.0020104616],"category_scores_gemma":[0.0010136497,0.00029976093,0.00036363807,0.0005254423,0.00050040695,0.00019690132,0.0005696624,0.0006350583,0.00042895752],"study_design_candidate":"bench_or_experimental","study_design_consensus":"bench_or_experimental","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00016334854,0.000035169414,0.0070481696,0.000047298276,0.000044484004,0.00011171499,0.00006394479,0.0023020331,0.97476655,0.00085580436,0.0001135458,0.014447891],"study_design_scores_gemma":[0.000027911516,0.00031059622,0.043296974,0.000016978081,0.0000862998,0.0009435004,0.00009285623,0.02019999,0.92854834,0.0021303229,0.0043091285,0.000036997775],"about_ca_topic_score_codex":0.0018518303,"about_ca_topic_score_gemma":0.0049968264,"teacher_disagreement_score":0.0020104616,"about_ca_system_score_codex":0.00058898755,"about_ca_system_score_gemma":0.00027218446,"threshold_uncertainty_score":0.006725669},"labels":[],"label_agreement":null},{"id":"W4400422940","doi":"10.1038/s41588-024-01827-2","title":"Metabolic gene function discovery platform GeneMAP identifies SLC25A48 as necessary for mitochondrial choline import","year":2024,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Metabolism and Genetic Disorders","field":"Biochemistry, Genetics and Molecular Biology","cited_by":26,"is_retracted":false,"has_abstract":true,"route_ca_aff":false,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"","funders":"National Institute of Diabetes and Digestive and Kidney Diseases; NIH Office of the Director; National Human Genome Research Institute; National Institute on Drug Abuse; National Institute of Mental Health; National Heart, Lung, and Blood Institute; National Institutes of Health; National Institute of Neurological Disorders and Stroke; National Institute of General Medical Sciences; Jewish General Hospital; National Institute on Aging; Damon Runyon Cancer Research Foundation; Boehringer Ingelheim Fonds; Common Fund; Servier; National Cancer Institute; Itä-Suomen Yliopisto","keywords":"Biology; Function (biology); Gene; Computational biology; Choline; Genetics; Mitochondrion; Bioinformatics; Biochemistry","score_opus":0.007219360195319663,"score_gpt":0.270405015781656,"score_spread":0.26318565558633633,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4400422940","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.83500576,0.003814253,0.06632539,0.0041459273,0.0005036237,0.00017885953,0.07268887,0.006184593,0.011152691],"genre_scores_gemma":[0.9198408,0.0012060081,0.044373546,0.00075160636,0.00011276982,0.0001382465,0.029882072,0.00034154166,0.0033534365],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9997545,0.000035656856,0.000013374714,0.00008628758,0.0000754847,0.000034769502],"domain_scores_gemma":[0.99942386,0.0002740708,0.00009897735,0.000051072246,0.000060450056,0.00009161288],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.000541335,0.00049040164,0.0005127777,0.00108047,0.00044546914,0.00073026185,0.00039171265,0.0005046771,0.008455452],"category_scores_gemma":[0.0013852213,0.00016250521,0.0007751114,0.0010062366,0.00025090482,0.00019842848,0.000579388,0.00062937546,0.0011968958],"study_design_candidate":"bench_or_experimental","study_design_consensus":"bench_or_experimental","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.002989116,0.00024723195,0.21654339,0.0015318866,0.0013865613,0.0127419615,0.000647661,0.010701962,0.4711127,0.009972514,0.07696214,0.19516292],"study_design_scores_gemma":[0.0012129105,0.0010325704,0.59089017,0.00040673293,0.0023837532,0.011911915,0.00046826998,0.076393224,0.11582692,0.02202461,0.17721346,0.0002354789],"about_ca_topic_score_codex":0.0028095786,"about_ca_topic_score_gemma":0.005849176,"teacher_disagreement_score":0.008455452,"about_ca_system_score_codex":0.0002889977,"about_ca_system_score_gemma":0.00077548117,"threshold_uncertainty_score":0.028286338},"labels":[],"label_agreement":null},{"id":"W4400457059","doi":"10.1038/s41588-024-01857-w","title":"Publisher Correction: Understanding the genetic complexity of puberty timing across the allele frequency spectrum","year":2024,"lang":"en","type":"erratum","venue":"Nature Genetics","topic":"RNA Research and Splicing","field":"Biochemistry, Genetics and Molecular Biology","cited_by":3,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Centre Hospitalier Universitaire Sainte-Justine; Centre for Global Health Research; University of Toronto; Mount Sinai Hospital; Lunenfeld-Tanenbaum Research Institute; Université de Montréal","funders":"","keywords":"Biology; Allele; Allele frequency; Genetics; Computational biology; Evolutionary biology; Gene","score_opus":0.0386145775385908,"score_gpt":0.311688981522797,"score_spread":0.2730744039842062,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4400457059","genre_codex":"editorial","genre_gemma":"editorial","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"editorial","genre_consensus":"editorial","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.00059342367,0.0010293927,0.0059553813,0.049022753,0.92701215,0.000021609561,0.0031895349,0.0011829123,0.011992784],"genre_scores_gemma":[0.043449625,0.0075710006,0.028771885,0.057313606,0.16004299,0.00019448063,0.009851388,0.006199336,0.6866057],"study_design_codex":"not_applicable","study_design_gemma":"not_applicable","domain_scores_codex":[0.9982887,0.00026584291,0.00022152603,0.0003655023,0.00073121546,0.00012726181],"domain_scores_gemma":[0.9869567,0.004416134,0.00058594,0.0012071347,0.00631679,0.0005173729],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0018347289,0.0018427714,0.0013398756,0.002205516,0.002479684,0.003087259,0.0030970266,0.004581295,0.095137075],"category_scores_gemma":[0.02755031,0.0008598456,0.00095735193,0.0024235628,0.0015406485,0.0017063373,0.0014328286,0.008135575,0.0342256],"study_design_candidate":"not_applicable","study_design_consensus":"not_applicable","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.000043079166,0.0000054909697,0.00015933417,0.00008829211,0.000012105719,0.00045698555,0.00004740593,0.00014599896,0.00016194924,0.0023198226,0.98523104,0.011328372],"study_design_scores_gemma":[0.00002613034,0.000010374441,0.0009933875,0.00017084354,0.00003378039,0.001317852,0.00006788083,0.00048145987,0.0008151279,0.0033861047,0.99266326,0.00003363714],"about_ca_topic_score_codex":0.018948661,"about_ca_topic_score_gemma":0.026040634,"teacher_disagreement_score":0.095137075,"about_ca_system_score_codex":0.002646912,"about_ca_system_score_gemma":0.0023110865,"threshold_uncertainty_score":0.3182652},"labels":[],"label_agreement":null},{"id":"W4400738648","doi":"10.1038/s41588-024-01826-3","title":"Integrated analyses highlight interactions between the three-dimensional genome and DNA, RNA and epigenomic alterations in metastatic prostate cancer","year":2024,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Epigenetics and DNA Methylation","field":"Biochemistry, Genetics and Molecular Biology","cited_by":38,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Canada's Michael Smith Genome Sciences Centre; Princess Margaret Cancer Centre; University of Toronto; University of British Columbia; University Health Network","funders":"Government of Ontario; American Association for Cancer Research; Movember Foundation; National Cancer Institute; National Institutes of Health; U.S. Department of Health and Human Services; Princess Margaret Cancer Foundation; University of Wisconsin Carbone Cancer Center; Stand Up To Cancer; U.S. Department of Defense","keywords":"Epigenomics; Biology; Prostate cancer; Computational biology; Genome; DNA; DNA methylation; Genetics; RNA; Cancer; Gene; Gene expression","score_opus":0.022222220278886935,"score_gpt":0.3306512547186385,"score_spread":0.30842903443975156,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4400738648","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9963856,0.00066849927,0.0019454224,0.000039817136,0.000002044598,0.0000047004432,0.0005485205,0.000031998272,0.0003734306],"genre_scores_gemma":[0.9980697,0.00019235394,0.0010005803,0.000023462577,0.0000030740443,0.0000036898948,0.0004666046,0.0000053995223,0.00023523798],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.99991655,0.000013463066,0.000004051805,0.00002668439,0.00002295506,0.00001618106],"domain_scores_gemma":[0.99991703,0.000017106267,0.000024319956,0.00000913757,0.000014790974,0.000017607315],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00013766158,0.000119825505,0.00015664802,0.00042858516,0.00013489858,0.00027871437,0.000108684035,0.00011683631,0.00051458663],"category_scores_gemma":[0.00022760821,0.0000913053,0.000117276875,0.00035925306,0.00013345704,0.00009332455,0.00027134805,0.00017222733,0.00007227846],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0002915032,0.000025413374,0.15025966,0.000082450606,0.00016327447,0.0002403,0.0001653493,0.0013895016,0.8256566,0.00024585807,0.0001842488,0.021295758],"study_design_scores_gemma":[0.000006037238,0.00013968938,0.93786347,0.000007706523,0.00011591674,0.0011511799,0.00020481397,0.0031841767,0.05530992,0.00044787524,0.0015593653,0.000009838976],"about_ca_topic_score_codex":0.0023830046,"about_ca_topic_score_gemma":0.0074635637,"teacher_disagreement_score":0.0023830046,"about_ca_system_score_codex":0.00015914589,"about_ca_system_score_gemma":0.00019706773,"threshold_uncertainty_score":0.0047382712},"labels":[],"label_agreement":null},{"id":"W4401091908","doi":"10.1038/s41588-024-01854-z","title":"Genetic factors associated with reasons for clinical trial stoppage","year":2024,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Statistical Methods in Clinical Trials","field":"Mathematics","cited_by":43,"is_retracted":false,"has_abstract":true,"route_ca_aff":false,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"","funders":"University of Toronto; European Molecular Biology Laboratory; Wellcome Trust; Wellcome; GlaxoSmithKline","keywords":"Biology; Genetics; Computational biology","score_opus":0.6127446181983821,"score_gpt":0.6109378820626427,"score_spread":0.0018067361357394507,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4401091908","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":"methods","model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":"methods","domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9677766,0.007655669,0.014477445,0.0039132163,0.00024536488,0.0002907983,0.0017793505,0.00036019497,0.0035013005],"genre_scores_gemma":[0.99533254,0.0004091134,0.0027796943,0.00034338294,0.000077039804,0.00009034628,0.00054157694,0.00008993245,0.00033651548],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9686123,0.014707712,0.0077872975,0.0032921792,0.004643135,0.00095739454],"domain_scores_gemma":[0.4219684,0.4238823,0.12995799,0.014682854,0.0058033583,0.0037050801],"candidate_categories":["metaresearch"],"consensus_categories":[],"category_scores_codex":[0.04125731,0.00036154885,0.0007193249,0.0028197984,0.00062195334,0.0017191923,0.0007534674,0.0015053169,0.0033291897],"category_scores_gemma":[0.21187505,0.00023641787,0.0018325355,0.0026871827,0.0012622548,0.0010471038,0.00063424755,0.002215328,0.00051258394],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0040822146,0.00016432925,0.9147061,0.00039121447,0.0012587293,0.0009897146,0.00051596697,0.0026539033,0.0021831465,0.0017895063,0.0025407216,0.06872433],"study_design_scores_gemma":[0.00040583243,0.0010088783,0.9531928,0.00040736992,0.0015740861,0.0035591908,0.0005427648,0.013335947,0.0038652467,0.011660597,0.010304975,0.00014233768],"about_ca_topic_score_codex":0.000805725,"about_ca_topic_score_gemma":0.0012911741,"teacher_disagreement_score":0.9587427,"about_ca_system_score_codex":0.0008886,"about_ca_system_score_gemma":0.0016939089,"threshold_uncertainty_score":0.2181921},"labels":[],"label_agreement":null},{"id":"W4401339987","doi":"10.1038/s41588-024-01835-2","title":"The Ruminant Telomere-to-Telomere (RT2T) Consortium","year":2024,"lang":"en","type":"review","venue":"Nature Genetics","topic":"Molecular Biology Techniques and Applications","field":"Biochemistry, Genetics and Molecular Biology","cited_by":30,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Alberta","funders":"Agricultural Research Service; National Institute of Food and Agriculture; Oxford Nanopore Technologies; Biotechnology and Biological Sciences Research Council; U.S. Department of Agriculture","keywords":"Telomere; Biology; Genetics; Telomere-binding protein; Ruminant; Computational biology; DNA; DNA-binding protein; Gene; Ecology; Transcription factor","score_opus":0.013104656990076855,"score_gpt":0.35038882443200303,"score_spread":0.3372841674419262,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4401339987","genre_codex":"review","genre_gemma":"review","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"review","genre_consensus":"review","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.00039197446,0.98536795,0.001042422,0.002323474,0.001998171,0.00004850009,0.00028244092,0.00006769769,0.008477443],"genre_scores_gemma":[0.0020449471,0.98085326,0.0012863256,0.0018523858,0.00063026417,0.00008182276,0.00064627803,0.000017143133,0.012587529],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.9998062,0.00003189604,0.000012863567,0.000031818206,0.00007908241,0.000038021528],"domain_scores_gemma":[0.99961025,0.00011942164,0.00005198714,0.000015943913,0.000115005925,0.00008752411],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.001383711,0.0008083177,0.00070342125,0.0010881718,0.00022042218,0.0008914104,0.0008143829,0.0012650298,0.00810946],"category_scores_gemma":[0.00089126173,0.00019270243,0.0003271455,0.001116506,0.00034950208,0.00071562006,0.00087686855,0.0015913198,0.0052652336],"study_design_candidate":"not_applicable","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00019672544,0.00008106571,0.00010824477,0.0023371987,0.000033833523,0.00012281096,0.000015163154,0.00019343793,0.001982782,0.0028862574,0.11511013,0.8769325],"study_design_scores_gemma":[0.000039193674,0.0000986268,0.00032701084,0.00076534564,0.000047636393,0.00021741654,0.000010215196,0.000033910335,0.00087778486,0.00041619095,0.9971615,0.0000051604643],"about_ca_topic_score_codex":0.0017631399,"about_ca_topic_score_gemma":0.002698421,"teacher_disagreement_score":0.00810946,"about_ca_system_score_codex":0.0006704719,"about_ca_system_score_gemma":0.0020829767,"threshold_uncertainty_score":0.027128816},"labels":[],"label_agreement":null},{"id":"W4401548680","doi":"10.1038/s41588-024-01876-7","title":"Chloroplast and whole-genome sequencing shed light on the evolutionary history and phenotypic diversification of peanuts","year":2024,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Peanut Plant Research Studies","field":"Agricultural and Biological Sciences","cited_by":38,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Ministry of Agriculture","funders":"National Key Research and Development Program of China; Chinese Academy of Agricultural Sciences; European Commission","keywords":"Biology; Arachis hypogaea; Domestication; Germplasm; Genome; Arachis; Evolutionary biology; Genetics; Botany; Gene","score_opus":0.022625585546059,"score_gpt":0.21736126532435102,"score_spread":0.194735679778292,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4401548680","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99142647,0.0016108798,0.0035750484,0.00010332785,0.000017544127,0.0000075498538,0.0018199696,0.000046264784,0.0013929964],"genre_scores_gemma":[0.98768604,0.0015886097,0.0052711577,0.000089743306,0.000016964901,0.000010937205,0.004054415,0.000033992463,0.0012481887],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9999112,0.000010209533,0.000004460104,0.000047897072,0.00001431762,0.000012020951],"domain_scores_gemma":[0.9998354,0.00003973608,0.00005074573,0.00002029596,0.000018669576,0.000035086407],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00020216934,0.00033938186,0.0001813363,0.00081636035,0.0002536548,0.00038122942,0.00018192061,0.00028231143,0.0009854387],"category_scores_gemma":[0.00021790604,0.00011719303,0.00029499788,0.0008872776,0.00026319263,0.00030575384,0.0004014906,0.00043093323,0.00020787338],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0002512066,0.000026957125,0.037492383,0.00018913376,0.00013652265,0.00031363143,0.00027256153,0.0006981475,0.9388437,0.0005890412,0.00014097891,0.02104566],"study_design_scores_gemma":[0.000019345156,0.0000989382,0.95070225,0.000057642705,0.00017872136,0.0010255506,0.0004611678,0.002086191,0.033524718,0.0011006126,0.010713876,0.000030990483],"about_ca_topic_score_codex":0.002564925,"about_ca_topic_score_gemma":0.0070521194,"teacher_disagreement_score":0.002564925,"about_ca_system_score_codex":0.0002899783,"about_ca_system_score_gemma":0.0002465761,"threshold_uncertainty_score":0.005099952},"labels":[],"label_agreement":null},{"id":"W4401702221","doi":"10.1038/s41588-024-01853-0","title":"Comprehensive molecular profiling of multiple myeloma identifies refined copy number and expression subtypes","year":2024,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Multiple Myeloma Research and Treatments","field":"Medicine","cited_by":75,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"McGill University; Alberta Cancer Foundation; Royal Victoria Hospital; Princess Margaret Cancer Centre","funders":"Principia Biopharma; Legend Biotech; Pharmacyclics; Kite Pharma; Genentech; EMD Serono; MorphoSys; Seagen; BeiGene; SkylineDx; Moderna; Pfizer; Incyte; Astex Pharmaceuticals; Baxalta; TG Therapeutics; Daewoong Pharmaceutical Company; Regeneron Pharmaceuticals; Eli Lilly and Company; AstraZeneca; CSL Behring; Swedish Orphan Biovitrum; Novo Nordisk; Teva Pharmaceutical Industries; Array BioPharma; National Cancer Institute; Gilead Sciences; Sanofi; Amgen; Vifor Pharma; Multiple Myeloma Research Foundation","keywords":"Biology; Multiple myeloma; Gene expression profiling; Computational biology; Profiling (computer programming); Expression (computer science); Genetics; Gene expression; Gene; Immunology; Computer science","score_opus":0.017007049811199958,"score_gpt":0.3285415472476464,"score_spread":0.31153449743644646,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4401702221","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.98984015,0.0009123561,0.0035360826,0.00015216279,0.0000075219327,0.00003405016,0.004117395,0.000111223104,0.0012890368],"genre_scores_gemma":[0.9919002,0.00037779126,0.0031083627,0.00011565451,0.000008796069,0.00003385966,0.0034477846,0.00003842232,0.0009693002],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9996414,0.000033751585,0.000024511843,0.00013911308,0.00010514435,0.000056089764],"domain_scores_gemma":[0.9995714,0.00007449962,0.00013481907,0.00009654713,0.00007480198,0.00004791935],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.000500903,0.00021860714,0.00033977552,0.0009403389,0.00029678698,0.0006908848,0.00027567623,0.00033609316,0.0013926087],"category_scores_gemma":[0.0011036026,0.00017497742,0.00031600127,0.0009695728,0.00019378141,0.00022414008,0.0004998408,0.00049711514,0.0004134359],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0011394931,0.00008815012,0.6339487,0.00011308999,0.0003428087,0.00031933316,0.0003115881,0.0017684356,0.29162955,0.0007006893,0.0019897518,0.06764847],"study_design_scores_gemma":[0.00003851929,0.00020471815,0.9608336,0.000019929244,0.00012609722,0.0013066878,0.00011396063,0.0027685438,0.02929706,0.0009644832,0.0043054977,0.00002083675],"about_ca_topic_score_codex":0.0020552434,"about_ca_topic_score_gemma":0.0036985856,"teacher_disagreement_score":0.0020552434,"about_ca_system_score_codex":0.00035592233,"about_ca_system_score_gemma":0.00024159579,"threshold_uncertainty_score":0.004658699},"labels":[],"label_agreement":null},{"id":"W4402172464","doi":"10.1038/s41588-024-01874-9","title":"In vivo CRISPR screens identify a dual function of MEN1 in regulating tumor–microenvironment interactions","year":2024,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Phagocytosis and Immune Regulation","field":"Immunology and Microbiology","cited_by":26,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Lunenfeld-Tanenbaum Research Institute; Mount Sinai Hospital; Princess Margaret Cancer Centre; University of Toronto; University Health Network","funders":"Canadian Institutes of Health Research; Terry Fox Research Institute; National Natural Science Foundation of China; Government of Canada; Princess Margaret Cancer Foundation","keywords":"Biology; MEN1; CRISPR; Tumor microenvironment; Function (biology); In vivo; Dual function; Computational biology; Genetics; Cancer research; Cell biology; Cancer; Gene; Multiple endocrine neoplasia; Computer science","score_opus":0.009708428185374502,"score_gpt":0.27761228532852716,"score_spread":0.2679038571431527,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4402172464","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.94956785,0.0016192568,0.038616646,0.00033888617,0.00008348627,0.00015583761,0.0029470583,0.0010407396,0.0056302533],"genre_scores_gemma":[0.98019695,0.0006413319,0.012426634,0.00013588986,0.0000074108298,0.000066100656,0.0009935349,0.00014852152,0.00538372],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9996278,0.00005802563,0.000042166626,0.00008477809,0.00013051312,0.00005665477],"domain_scores_gemma":[0.9996966,0.00009549856,0.00009408454,0.00003624841,0.00001681735,0.000060864135],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0003314865,0.0006612505,0.00042650392,0.0004864272,0.00026505484,0.00067668164,0.00037530297,0.00057617744,0.0028971003],"category_scores_gemma":[0.00020257803,0.00026722817,0.0004026729,0.00018457009,0.0004009106,0.0002141224,0.0005979574,0.00074815203,0.0007315821],"study_design_candidate":"bench_or_experimental","study_design_consensus":"bench_or_experimental","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.000041420815,0.000014565124,0.0001738969,0.000024945703,0.000007970076,0.00007217968,0.000010367684,0.00016302019,0.9982004,0.00017032343,0.000048281596,0.0010726271],"study_design_scores_gemma":[0.000008437577,0.00007707324,0.0015862194,0.000004589112,0.00001638654,0.0002529389,0.000015620139,0.0011454218,0.99476695,0.00006113817,0.002058898,0.0000063277644],"about_ca_topic_score_codex":0.00070793985,"about_ca_topic_score_gemma":0.0023049705,"teacher_disagreement_score":0.0028971003,"about_ca_system_score_codex":0.00053690316,"about_ca_system_score_gemma":0.0003070901,"threshold_uncertainty_score":0.009691834},"labels":[],"label_agreement":null},{"id":"W4402371498","doi":"10.1038/s41588-024-01903-7","title":"Defining and pursuing diversity in human genetic studies","year":2024,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Race, Genetics, and Society","field":"Biochemistry, Genetics and Molecular Biology","cited_by":7,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Toronto; Terry Fox Research Institute; McGill Genome Centre","funders":"National Human Genome Research Institute; U.S. Department of Health and Human Services","keywords":"Biology; Diversity (politics); Evolutionary biology; Human genetic variation; Computational biology; Genetic diversity; Genetics; Human genome; Genome; Gene; Anthropology; Demography; Population; Sociology","score_opus":0.012606944068531523,"score_gpt":0.2910532533322448,"score_spread":0.2784463092637133,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4402371498","genre_codex":"methods","genre_gemma":"empirical","domain_codex":null,"domain_gemma":"methods","model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":null,"domain_candidate":"methods","domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.31611678,0.04860182,0.33288348,0.24382481,0.002445871,0.00024384797,0.00024436117,0.000322514,0.055316526],"genre_scores_gemma":[0.90745103,0.0068470915,0.067952946,0.014080029,0.0014676667,0.00016543719,0.000060559414,0.00012654677,0.0018487587],"study_design_codex":"theoretical_or_conceptual","study_design_gemma":"theoretical_or_conceptual","domain_scores_codex":[0.953971,0.035184957,0.0014479033,0.0032072007,0.0045890557,0.0015998075],"domain_scores_gemma":[0.90008765,0.062113825,0.0060143387,0.015521202,0.008162318,0.008100738],"candidate_categories":["metaresearch"],"consensus_categories":[],"category_scores_codex":[0.08085527,0.0006026214,0.001963337,0.005815547,0.006095981,0.008829752,0.0025252094,0.003033184,0.0013369534],"category_scores_gemma":[0.09090778,0.00068578316,0.0005340615,0.0032166524,0.036495097,0.014062734,0.018760547,0.007180076,0.00020083712],"study_design_candidate":"theoretical_or_conceptual","study_design_consensus":"theoretical_or_conceptual","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00017150209,0.00009489327,0.04159094,0.00048791492,0.0002971602,0.00047569443,0.022642817,0.0012227929,0.0035340732,0.79095846,0.0044655683,0.1340582],"study_design_scores_gemma":[0.000019954206,0.000047554655,0.0048811645,0.00025944322,0.000053979995,0.00041456614,0.0059238574,0.0007000626,0.000991344,0.9635392,0.023136009,0.000032953096],"about_ca_topic_score_codex":0.0026280794,"about_ca_topic_score_gemma":0.004502533,"teacher_disagreement_score":0.91914475,"about_ca_system_score_codex":0.0033890312,"about_ca_system_score_gemma":0.0070339846,"threshold_uncertainty_score":0.42760867},"labels":[],"label_agreement":null},{"id":"W4402533801","doi":"10.1038/s41588-024-01899-0","title":"Five latent factors underlie response to immunotherapy","year":2024,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Cancer Immunotherapy and Biomarkers","field":"Medicine","cited_by":33,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Princess Margaret Cancer Centre","funders":"Ministerio de Economía y Competitividad; Centres de Recerca de Catalunya; Generalitat de Catalunya; European Commission; Institute for Research in Biomedicine","keywords":"Biology; Immunotherapy; Tumor microenvironment; Immune system; Oncology; Transcriptome; Cohort; Immunology; Computational biology; Cancer research; Bioinformatics; Internal medicine; Medicine; Genetics; Gene; Gene expression","score_opus":0.014919407951357636,"score_gpt":0.30722133498530424,"score_spread":0.2923019270339466,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4402533801","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99204636,0.0011791232,0.0042063566,0.0003961156,0.000011854755,0.000030111425,0.0011307065,0.00008461388,0.0009148859],"genre_scores_gemma":[0.9986469,0.00015491879,0.0003936863,0.000047074987,0.000013022492,0.000011403809,0.0005905734,0.000011217592,0.0001311859],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9991314,0.00022564262,0.0000926099,0.00027798358,0.00013394587,0.00013838187],"domain_scores_gemma":[0.99602413,0.0014583254,0.001559789,0.00056206516,0.00015010913,0.00024555062],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0012447989,0.00020675024,0.00049828505,0.0006354958,0.00019607997,0.0013405833,0.0003325992,0.0005004973,0.0019407176],"category_scores_gemma":[0.0050341403,0.00017735356,0.0004910296,0.0008397596,0.0006052243,0.00050132885,0.0005737399,0.0007220109,0.0004278545],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0008436682,0.000109939356,0.9586605,0.00005625567,0.00027856507,0.000091036854,0.00020462579,0.0012262667,0.014725205,0.0009049472,0.00041415766,0.022484804],"study_design_scores_gemma":[0.000023379635,0.00020240559,0.987491,0.000015025283,0.00010889948,0.00028766424,0.00015630343,0.0055593634,0.001963346,0.0034091526,0.00076302834,0.00002034094],"about_ca_topic_score_codex":0.0007910286,"about_ca_topic_score_gemma":0.00053433113,"teacher_disagreement_score":0.0019407176,"about_ca_system_score_codex":0.00037553255,"about_ca_system_score_gemma":0.0004957438,"threshold_uncertainty_score":0.006583214},"labels":[],"label_agreement":null},{"id":"W4402992718","doi":"10.1038/s41588-024-01934-0","title":"Valid inference for machine learning-assisted genome-wide association studies","year":2024,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Genetic Associations and Epidemiology","field":"Biochemistry, Genetics and Molecular Biology","cited_by":23,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Jewish General Hospital; University of Toronto","funders":"Division of Graduate Education; National Human Genome Research Institute; National Institute on Aging; U.S. Department of Health and Human Services; National Institutes of Health; Wisconsin Alumni Research Foundation; University of Wisconsin-Madison","keywords":"Biology; Inference; Genome-wide association study; Computational biology; Association (psychology); Evolutionary biology; Genetic association; Genetics; Artificial intelligence; Single-nucleotide polymorphism; Computer science; Gene; Genotype; Epistemology","score_opus":0.021570010754279778,"score_gpt":0.3309692256446784,"score_spread":0.3093992148903986,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4402992718","genre_codex":"methods","genre_gemma":"methods","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"methods","genre_consensus":"methods","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.0049542617,0.00082979666,0.990973,0.0008826339,0.0001761879,0.000103794344,0.0008204895,0.00075308507,0.00050682214],"genre_scores_gemma":[0.35328352,0.0010961037,0.63185453,0.0023649144,0.0011464949,0.001141472,0.005950661,0.0005956992,0.0025666743],"study_design_codex":"design_other","study_design_gemma":"theoretical_or_conceptual","domain_scores_codex":[0.94959193,0.036997337,0.002901435,0.0055701653,0.0039716545,0.00096750434],"domain_scores_gemma":[0.65285224,0.30644315,0.004789149,0.028733823,0.005815548,0.001366061],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.05847357,0.0013593315,0.004030967,0.0036086624,0.0029891192,0.0043723863,0.0067327274,0.003297938,0.0055539263],"category_scores_gemma":[0.28589755,0.0019067652,0.003568496,0.0036420757,0.004400315,0.0049975044,0.005914794,0.007784793,0.0015056868],"study_design_candidate":"theoretical_or_conceptual","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0029810334,0.00047138333,0.04959248,0.0021124103,0.0043511163,0.0021833805,0.00067462685,0.24243587,0.0036205933,0.28691766,0.017694505,0.38696498],"study_design_scores_gemma":[0.00022776981,0.00010131717,0.0016133434,0.00016412357,0.00040792892,0.00030528422,0.00005246495,0.412316,0.0016223461,0.57904303,0.0041088928,0.000037451304],"about_ca_topic_score_codex":0.0039738095,"about_ca_topic_score_gemma":0.00425001,"teacher_disagreement_score":0.05847357,"about_ca_system_score_codex":0.0015777263,"about_ca_system_score_gemma":0.004776974,"threshold_uncertainty_score":0.30924147},"labels":[],"label_agreement":null},{"id":"W4403401639","doi":"10.1038/s41588-024-01950-0","title":"Parsing the spectrum of allelic architectures in diabetes","year":2024,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Diabetes and associated disorders","field":"Biochemistry, Genetics and Molecular Biology","cited_by":1,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"McGill University Health Centre","funders":"","keywords":"Biology; Parsing; Allele; Computational biology; Genetics; Evolutionary biology; Gene; Artificial intelligence; Computer science","score_opus":0.003137856658634135,"score_gpt":0.22997395367655385,"score_spread":0.2268360970179197,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4403401639","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.8628155,0.005436874,0.1070365,0.0054266457,0.00017893095,0.000045151522,0.0041021993,0.00089397246,0.014064214],"genre_scores_gemma":[0.96681887,0.0011700777,0.028413363,0.00068978907,0.00011617878,0.000022446548,0.0017020189,0.0002426325,0.00082466064],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9983706,0.00079732377,0.0000980978,0.00036551588,0.00017865456,0.0001899301],"domain_scores_gemma":[0.9890564,0.007914152,0.00092318497,0.0009777053,0.0006866072,0.00044197257],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0026747037,0.0006589285,0.0007589575,0.003037422,0.0007662019,0.0032477921,0.0008555129,0.0011792072,0.0029101907],"category_scores_gemma":[0.012500384,0.0005518723,0.0006181346,0.002092941,0.0011468787,0.0023954087,0.0022275522,0.0020885805,0.00057909265],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0020804142,0.00037641858,0.5064892,0.00042516424,0.0006726783,0.0039432854,0.002565284,0.02309272,0.060050745,0.15498331,0.0126151545,0.2327056],"study_design_scores_gemma":[0.0001228558,0.0001121856,0.1339307,0.00033498285,0.00046120488,0.003852929,0.0015671077,0.06215185,0.008090165,0.7696102,0.019620767,0.00014504681],"about_ca_topic_score_codex":0.0022593902,"about_ca_topic_score_gemma":0.0038298029,"teacher_disagreement_score":0.0032477921,"about_ca_system_score_codex":0.0004904189,"about_ca_system_score_gemma":0.00060180435,"threshold_uncertainty_score":0.014145315},"labels":[],"label_agreement":null},{"id":"W4403609354","doi":"10.1038/s41588-024-01941-1","title":"Pushing the boundaries of rare disease diagnostics with the help of the first Undiagnosed Hackathon","year":2024,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Biomedical and Engineering Education","field":"Engineering","cited_by":7,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"McGill University; Hospital for Sick Children","funders":"Eunice Kennedy Shriver National Institute of Child Health and Human Development; National Institute of Neurological Disorders and Stroke; Uppsala Multidisciplinary Center for Advanced Computational Science; Science for Life Laboratory; Vetenskapsrådet; National Human Genome Research Institute; Chan Zuckerberg Initiative; Bertil Hållstens Forskningsstiftelse; Hjärnfonden; Knut och Alice Wallenbergs Stiftelse; Karolinska Institutet; Oxford Nanopore Technologies","keywords":"Medical diagnosis; Multidisciplinary approach; General partnership; Biology; Disease; Precision medicine; Genomic medicine; Data science; Computational biology; Medical physics; Bioinformatics; Genetics; Medicine; Computer science; Pathology","score_opus":0.003266688477648099,"score_gpt":0.19337278368275945,"score_spread":0.19010609520511135,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4403609354","genre_codex":"commentary","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":null,"domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.07128582,0.031334158,0.054755062,0.7608168,0.013604297,0.00012359524,0.00056301,0.0015741757,0.065943],"genre_scores_gemma":[0.6391757,0.034306362,0.07111245,0.20712827,0.016456546,0.00016994495,0.0007899719,0.0011953843,0.029665368],"study_design_codex":"design_other","study_design_gemma":"observational","domain_scores_codex":[0.99675936,0.0012211798,0.0002175582,0.0005917786,0.0006809547,0.000529216],"domain_scores_gemma":[0.98007697,0.01120549,0.0011402234,0.0012270464,0.0027136975,0.0036365788],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0057051415,0.0006935014,0.0008519661,0.0031468049,0.0022365449,0.0045885094,0.0016024329,0.0050078533,0.017816618],"category_scores_gemma":[0.04359163,0.0005344572,0.00070451404,0.00055145065,0.0036084757,0.0065738396,0.0054970686,0.012424418,0.0056373924],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0006536102,0.0005106737,0.07587083,0.00067892997,0.00010776657,0.012248213,0.0053544743,0.0012770697,0.006436531,0.05033944,0.2678673,0.5786551],"study_design_scores_gemma":[0.00018092526,0.00073300034,0.040501997,0.008436364,0.00027749455,0.033060025,0.01028182,0.005317426,0.007844546,0.31771275,0.57515186,0.00050166895],"about_ca_topic_score_codex":0.0055446876,"about_ca_topic_score_gemma":0.005433801,"teacher_disagreement_score":0.017816618,"about_ca_system_score_codex":0.0022094124,"about_ca_system_score_gemma":0.005556587,"threshold_uncertainty_score":0.05960256},"labels":[],"label_agreement":null},{"id":"W4403609401","doi":"10.1038/s41588-024-01951-z","title":"Genomic analysis of intracranial and subcortical brain volumes yields polygenic scores accounting for variation across ancestries","year":2024,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Genetic Associations and Epidemiology","field":"Biochemistry, Genetics and Molecular Biology","cited_by":19,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Hospital for Sick Children; SickKids Foundation; University of Toronto; Université de Montréal; Centre Hospitalier Universitaire Sainte-Justine; University of Calgary; McGill University; Douglas College","funders":"Cilag; National Institute of Neurological Disorders and Stroke; National Institute of Mental Health; National Institute on Aging; Avid Radiopharmaceuticals; University of California, San Diego; Genentech; Hector Stiftung II; Neuraxpharm; European College of Neuropsychopharmacology; Fresenius Medical Care North America; Eisai; National Institute of Biomedical Imaging and Bioengineering; Daimler und Benz Stiftung; Hector Stiftung; Servier; Eli Lilly and Company; Lundbeckfonden; European Commission; Sunovion; H. Lundbeck A/S; Northwell Health; National Institutes of Health; National Heart, Lung, and Blood Institute; Fondation FondaMental; École Polytechnique Fédérale de Lausanne; Pfizer; Biogen; Siemens Medical Solutions USA","keywords":"Biology; Putamen; Genome-wide association study; Neuroscience; Brain size; Thalamus; Globus pallidus; Brain morphometry; Nucleus accumbens; Caudate nucleus; Multifactorial Inheritance; Neuroanatomy; Genetics; Gene; Basal ganglia; Single-nucleotide polymorphism; Central nervous system; Genotype; Medicine","score_opus":0.008385336469411234,"score_gpt":0.29903413697088915,"score_spread":0.2906488005014779,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4403609401","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9865573,0.00014191742,0.010949261,0.00014806671,0.000015899115,0.00000872961,0.0010036052,0.00013008379,0.0010451924],"genre_scores_gemma":[0.9954526,0.000069547816,0.0033748187,0.000027957356,0.000014263378,0.000010299797,0.00053855765,0.00004671847,0.0004653207],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9987978,0.00053831446,0.00006230081,0.00036884882,0.0001232102,0.000109585824],"domain_scores_gemma":[0.9978467,0.0010879615,0.0004333018,0.00030663083,0.00016648462,0.00015876441],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0012793324,0.00085774454,0.0005060722,0.0021270511,0.0005431665,0.0008162549,0.00045697863,0.00049973483,0.0034981854],"category_scores_gemma":[0.0035612076,0.00028692465,0.00093729945,0.0025202709,0.0004978086,0.0002966351,0.0008390745,0.00072886824,0.0003852208],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0005344348,0.00009484423,0.89364624,0.000051221064,0.0019861255,0.0011683565,0.00060527725,0.0029493344,0.061893415,0.001957917,0.0008339008,0.03427898],"study_design_scores_gemma":[0.000009981299,0.000064896274,0.99317497,0.000006496256,0.00018928635,0.0004439561,0.00011327192,0.003052817,0.0014352538,0.0011492952,0.00034560665,0.000014156107],"about_ca_topic_score_codex":0.00716012,"about_ca_topic_score_gemma":0.006882604,"teacher_disagreement_score":0.00716012,"about_ca_system_score_codex":0.00023659895,"about_ca_system_score_gemma":0.00034214792,"threshold_uncertainty_score":0.014236927},"labels":[],"label_agreement":null},{"id":"W4404224754","doi":"10.1038/s41588-024-01974-6","title":"Toward advances in retinoblastoma genetics in Kenya","year":2024,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Ocular Oncology and Treatments","field":"Medicine","cited_by":0,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"SickKids Foundation; Public Health Ontario","funders":"","keywords":"Retinoblastoma; Cancer genetics; Biology; Genetics; Medical genetics; Cancer; Evolutionary biology; Gene","score_opus":0.009681139028130368,"score_gpt":0.3142051373553408,"score_spread":0.3045239983272104,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4404224754","genre_codex":"commentary","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":null,"domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.08011261,0.24499536,0.0112483,0.57641053,0.0043640607,0.00023646951,0.0011377998,0.00024817773,0.08124663],"genre_scores_gemma":[0.48678464,0.3770975,0.043872222,0.068999484,0.0032055646,0.00020174685,0.0011134499,0.0002022591,0.01852325],"study_design_codex":"design_other","study_design_gemma":"observational","domain_scores_codex":[0.9984281,0.00066870794,0.00015079937,0.00015398231,0.00024034764,0.00035811195],"domain_scores_gemma":[0.9939174,0.002690706,0.0006247058,0.00023431116,0.0015711454,0.00096182566],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0055188313,0.00048772994,0.00049974484,0.0023921586,0.0018623077,0.0019615775,0.0009222584,0.002367715,0.008018439],"category_scores_gemma":[0.010096195,0.00035179727,0.00031601632,0.0014952096,0.0023568638,0.0035446282,0.0019116519,0.0041633924,0.0010640722],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00067363627,0.00052199315,0.072110996,0.0021529335,0.00011347277,0.008699854,0.0069070044,0.0020041957,0.016624538,0.14318794,0.09017807,0.65682536],"study_design_scores_gemma":[0.0001983978,0.00040916938,0.043069266,0.008938078,0.00024429846,0.008453675,0.007858585,0.0011894143,0.0052585336,0.05496003,0.8692691,0.00015154507],"about_ca_topic_score_codex":0.043702442,"about_ca_topic_score_gemma":0.08142031,"teacher_disagreement_score":0.043702442,"about_ca_system_score_codex":0.005489462,"about_ca_system_score_gemma":0.01613942,"threshold_uncertainty_score":0.08689618},"labels":[],"label_agreement":null},{"id":"W4404566931","doi":"10.1038/s41588-024-01988-0","title":"Luminal breast epithelial cells of BRCA1 or BRCA2 mutation carriers and noncarriers harbor common breast cancer copy number alterations","year":2024,"lang":"en","type":"article","venue":"Nature Genetics","topic":"BRCA gene mutations in cancer","field":"Biochemistry, Genetics and Molecular Biology","cited_by":29,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"BC Cancer Agency; University of British Columbia","funders":"National Cancer Institute; National Human Genome Research Institute","keywords":"Biology; Loss of heterozygosity; Cancer research; Breast cancer; BRCA2 Protein; Somatic cell; Germline mutation; Myoepithelial cell; Germline; Population; Genetics; Allele; Cancer; Mutation; Immunology; Gene; Medicine","score_opus":0.0054188587088345236,"score_gpt":0.2848017929453763,"score_spread":0.27938293423654176,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4404566931","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.999329,0.00017406676,0.00006940054,0.0000068593213,0.0000013375301,0.0000030342874,0.00014579415,0.000005072914,0.00026551884],"genre_scores_gemma":[0.99906665,0.00009282079,0.00017959595,0.000011965661,0.000002324386,0.000006493709,0.00031330157,0.0000039428505,0.00032285342],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9998516,0.000018344634,0.000014923415,0.000048160102,0.000030326986,0.00003669408],"domain_scores_gemma":[0.99981314,0.00005697838,0.00004038885,0.000025943946,0.000014845579,0.00004866272],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00016846985,0.00015849697,0.00028238652,0.0010645812,0.00022876414,0.00028758304,0.00016408498,0.00024775486,0.0027281656],"category_scores_gemma":[0.00065088813,0.00013024402,0.00009942067,0.00030524356,0.00025180087,0.00016801842,0.00032428218,0.00011032192,0.0002872597],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0013725973,0.000074283824,0.45011532,0.0000610784,0.00006670473,0.001487997,0.00077677885,0.00007009027,0.5344717,0.00020176258,0.00011751408,0.01118426],"study_design_scores_gemma":[0.000010450357,0.00016988418,0.9838081,0.0000045116794,0.000025031308,0.0047078934,0.00034241084,0.00018088112,0.010135559,0.000111564696,0.00049780303,0.0000058660503],"about_ca_topic_score_codex":0.0013955629,"about_ca_topic_score_gemma":0.0017139846,"teacher_disagreement_score":0.0027281656,"about_ca_system_score_codex":0.00016510763,"about_ca_system_score_gemma":0.00011161009,"threshold_uncertainty_score":0.009126604},"labels":[],"label_agreement":null},{"id":"W4404595278","doi":"10.1038/s41588-024-01975-5","title":"Genome-wide association study reveals mechanisms underlying dilated cardiomyopathy and myocardial resilience","year":2024,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Genetic Associations and Epidemiology","field":"Biochemistry, Genetics and Molecular Biology","cited_by":49,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Université de Montréal; Montreal Heart Institute","funders":"HORIZON EUROPE European Innovation Council; National Heart, Lung, and Blood Institute; National Institutes of Health; Associação Fundo de Incentivo à Pesquisa; Agence Nationale de la Recherche; Deutsche Forschungsgemeinschaft; European Commission; Sir Jules Thorn Charitable Trust; British Heart Foundation; Foundation for the National Institutes of Health; Amsterdam University Medical Centers; Hartstichting; American Heart Association; U.S. Department of Veterans Affairs; ZonMw; Aarne Koskelon Säätiö","keywords":"Mendelian randomization; Genome-wide association study; Biology; Dilated cardiomyopathy; Genetic architecture; Heart failure; Genome; Genetic association; Genetics; Disease; Cardiomyopathy; Quantitative trait locus; Gene; Single-nucleotide polymorphism; Internal medicine; Genetic variants; Medicine; Genotype","score_opus":0.010932941119844629,"score_gpt":0.28005460342647803,"score_spread":0.2691216623066334,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4404595278","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99686843,0.0008649064,0.0013428979,0.00016672062,0.000008280339,0.000005613208,0.00023455209,0.000022571663,0.00048605909],"genre_scores_gemma":[0.9991291,0.00021543409,0.00037331317,0.00002948455,0.000008133367,0.000003441606,0.00013088464,0.0000045760057,0.00010569594],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99921286,0.00031040263,0.000055495984,0.00023907928,0.000095742995,0.00008631744],"domain_scores_gemma":[0.998869,0.00043526312,0.0003552541,0.00017079906,0.000050175717,0.000119518394],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0013634455,0.00029307735,0.00039039634,0.0011345359,0.00037422898,0.00054707297,0.00030465133,0.00039361365,0.0016793469],"category_scores_gemma":[0.0024822801,0.00018330646,0.00055704615,0.0011306551,0.00047652022,0.00019873712,0.00070945977,0.0004659731,0.00015977187],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00066196505,0.000051416384,0.96874577,0.000039095943,0.0010504031,0.00079487066,0.00021459135,0.0003553463,0.018240608,0.00048637594,0.0002651437,0.009094371],"study_design_scores_gemma":[0.000017448305,0.000047800535,0.99736685,0.0000069195776,0.00023430464,0.00045378233,0.000080253696,0.00044618634,0.00057720597,0.00047779366,0.00028457618,0.000006891786],"about_ca_topic_score_codex":0.0012018352,"about_ca_topic_score_gemma":0.0016020004,"teacher_disagreement_score":0.0016793469,"about_ca_system_score_codex":0.00013914323,"about_ca_system_score_gemma":0.00020366315,"threshold_uncertainty_score":0.007210672},"labels":[],"label_agreement":null},{"id":"W4404595279","doi":"10.1038/s41588-024-01952-y","title":"Genome-wide association analysis provides insights into the molecular etiology of dilated cardiomyopathy","year":2024,"lang":"en","type":"article","venue":"Nature Genetics","topic":"RNA modifications and cancer","field":"Biochemistry, Genetics and Molecular Biology","cited_by":53,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Université de Montréal; Montreal Heart Institute","funders":"Medical Research Council; University College London; Imperial College London; Rosetrees Trust; Department of Health and Social Care; National Institute for Health and Care Research; Wellcome Trust; British Heart Foundation; Cancer Research UK; Novo Nordisk Fonden; Israel Cancer Research Fund","keywords":"Dilated cardiomyopathy; Biology; Penetrance; Genetics; Genome-wide association study; Biobank; Cardiomyopathy; Genetic association; Multifactorial Inheritance; Population; Heart failure; Etiology; Bioinformatics; Computational biology; Gene; Single-nucleotide polymorphism; Internal medicine; Medicine; Phenotype; Genotype","score_opus":0.0036997288233919035,"score_gpt":0.23981724442592145,"score_spread":0.23611751560252955,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4404595279","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9803105,0.0069441693,0.008527117,0.00054362335,0.00003673696,0.000011078616,0.0016775003,0.00008654163,0.001862736],"genre_scores_gemma":[0.99534744,0.0016301081,0.0020908639,0.0001097574,0.000037634632,0.000006698521,0.00049850706,0.000010851993,0.00026811604],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9995153,0.00017508307,0.000033205084,0.000161456,0.00007969278,0.00003524336],"domain_scores_gemma":[0.99900275,0.00057307334,0.00025183923,0.00008022841,0.000036827456,0.00005527654],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00086645223,0.0003186423,0.0004378763,0.0011633431,0.00022759693,0.00049320667,0.00019848281,0.00040450558,0.0018881569],"category_scores_gemma":[0.0013613455,0.00014729406,0.00031380818,0.001239394,0.00038950454,0.00020485214,0.00047928418,0.00043864857,0.00022877482],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0009205338,0.00008418209,0.82334906,0.00024879278,0.0016136514,0.0015885115,0.00019342215,0.0016211697,0.10762826,0.0016496024,0.001057156,0.06004556],"study_design_scores_gemma":[0.000038278016,0.00016671719,0.9802829,0.000036274443,0.00057102635,0.0019075933,0.0001175534,0.0018652576,0.0069527472,0.0032400168,0.0047982577,0.000023442482],"about_ca_topic_score_codex":0.0006770281,"about_ca_topic_score_gemma":0.0015053342,"teacher_disagreement_score":0.0018881569,"about_ca_system_score_codex":0.00014185865,"about_ca_system_score_gemma":0.00017568911,"threshold_uncertainty_score":0.006316483},"labels":[],"label_agreement":null},{"id":"W4404860326","doi":"10.1038/s41588-024-01989-z","title":"Characterizing the evolutionary dynamics of cancer proliferation in single-cell clones with SPRINTER","year":2024,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Cancer Genomics and Diagnostics","field":"Biochemistry, Genetics and Molecular Biology","cited_by":21,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of British Columbia","funders":"Rosetrees Trust; Wellcome Trust; Francis Crick Institute; Cancer Research UK; Medical Research Council; Wellcome; Breast Cancer Research Foundation","keywords":"Biology; clone (Java method); Cell growth; Metastasis; Cancer; Gene; Genetics; Cancer research; Computational biology","score_opus":0.0047922741817074425,"score_gpt":0.23311495594185486,"score_spread":0.22832268176014742,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4404860326","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.6993853,0.0015102274,0.28541902,0.00021967532,0.000066561195,0.00010055195,0.0066049956,0.005083569,0.0016102097],"genre_scores_gemma":[0.7514067,0.00060178805,0.22697194,0.00015142192,0.000039514034,0.00026268396,0.01825268,0.0006590353,0.0016541369],"study_design_codex":"simulation_or_modeling","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99941564,0.000092727474,0.00003163564,0.00030529976,0.0001197213,0.0000349077],"domain_scores_gemma":[0.99812454,0.0010031088,0.0002788318,0.00036179693,0.00017045671,0.00006124672],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0018466709,0.0005506019,0.00074796774,0.001253864,0.00043281648,0.0010880947,0.0007665835,0.0008519832,0.0009532547],"category_scores_gemma":[0.005194363,0.00043423063,0.0009929754,0.001133623,0.00049109396,0.0007020513,0.0008793766,0.00094367366,0.00052537845],"study_design_candidate":"bench_or_experimental","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0011993654,0.00023566226,0.23070663,0.0009996431,0.0012295621,0.0007669912,0.0013923334,0.2832709,0.2599934,0.011691127,0.00613578,0.20237866],"study_design_scores_gemma":[0.000057904614,0.00023588847,0.041475326,0.000035013574,0.0001719687,0.0006881464,0.00017844896,0.87499696,0.061129496,0.011031794,0.009931621,0.000067430534],"about_ca_topic_score_codex":0.0020375184,"about_ca_topic_score_gemma":0.003837019,"teacher_disagreement_score":0.0020375184,"about_ca_system_score_codex":0.00049126835,"about_ca_system_score_gemma":0.00042842262,"threshold_uncertainty_score":0.009766221},"labels":[],"label_agreement":null},{"id":"W4404994910","doi":"10.1038/s41588-024-02047-4","title":"Publisher Correction: Genome-wide association study reveals mechanisms underlying dilated cardiomyopathy and myocardial resilience","year":2024,"lang":"en","type":"erratum","venue":"Nature Genetics","topic":"Cardiovascular Disease and Adiposity","field":"Medicine","cited_by":2,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Université de Montréal; Montreal Heart Institute","funders":"","keywords":"Dilated cardiomyopathy; Biology; Resilience (materials science); Genome-wide association study; Association (psychology); Computational biology; Cardiomyopathy; Genetics; Internal medicine; Cardiology; Heart failure; Single-nucleotide polymorphism; Gene; Medicine; Genotype; Physics; Psychology","score_opus":0.009949159905292763,"score_gpt":0.2610041859658018,"score_spread":0.25105502606050906,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4404994910","genre_codex":"editorial","genre_gemma":"other","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"other","genre_consensus":null,"domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.00013655204,0.0005573191,0.0006829481,0.028219273,0.96808773,0.000015945963,0.00073961006,0.00024663453,0.0013140175],"genre_scores_gemma":[0.021226473,0.0082878135,0.009589216,0.09429381,0.58317506,0.00032815436,0.0050453898,0.0020287083,0.2760254],"study_design_codex":"not_applicable","study_design_gemma":"not_applicable","domain_scores_codex":[0.99559575,0.00076385395,0.00094785827,0.00065461244,0.0016790986,0.00035886467],"domain_scores_gemma":[0.9722741,0.008494647,0.0012079627,0.0021131795,0.014646469,0.0012635954],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.004372758,0.0027453366,0.0025347483,0.0035898755,0.002968268,0.0037263082,0.004472204,0.0065566325,0.05592737],"category_scores_gemma":[0.05915151,0.001462454,0.0020487625,0.002646493,0.0018744762,0.0018062708,0.0017845928,0.012835465,0.023769557],"study_design_candidate":"not_applicable","study_design_consensus":"not_applicable","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.000045728608,0.000008310685,0.00013436002,0.00013266607,0.000026884563,0.00058388046,0.00003186799,0.000050778777,0.00007673732,0.0006995753,0.99303776,0.005171383],"study_design_scores_gemma":[0.0001125068,0.000039672803,0.002115802,0.00050096127,0.00014865934,0.0025112643,0.00012400547,0.0005606034,0.00060103025,0.0027206002,0.9904813,0.000083698826],"about_ca_topic_score_codex":0.015300836,"about_ca_topic_score_gemma":0.022695774,"teacher_disagreement_score":0.05592737,"about_ca_system_score_codex":0.0028423893,"about_ca_system_score_gemma":0.004682256,"threshold_uncertainty_score":0.1870957},"labels":[],"label_agreement":null},{"id":"W4405995908","doi":"10.1038/s41588-024-01997-z","title":"Dissecting tumor transcriptional heterogeneity from single-cell RNA-seq data by generalized binary covariance decomposition","year":2025,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Single-cell and spatial transcriptomics","field":"Biochemistry, Genetics and Molecular Biology","cited_by":12,"is_retracted":false,"has_abstract":false,"route_ca_aff":false,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"","funders":"National Institute of Diabetes and Digestive and Kidney Diseases; National Institute of General Medical Sciences; National Human Genome Research Institute; Government of Ontario; Neuroendocrine Tumor Research Foundation; University of Chicago; Leona M. and Harry B. Helmsley Charitable Trust; National Cancer Institute; National Institutes of Health; U.S. Department of Health and Human Services","keywords":"Biology; Computational biology; Bayes' theorem; Tumor heterogeneity; Gene expression; Gene expression profiling; False discovery rate; Gene; Genetics; Cancer; Bayesian probability; Computer science; Artificial intelligence","score_opus":0.01785443821445935,"score_gpt":0.28061615917087124,"score_spread":0.26276172095641187,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4405995908","genre_codex":"methods","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":null,"domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.16729163,0.00024869977,0.82911366,0.000240392,0.000034286884,0.000036424623,0.0016170437,0.0007753764,0.0006423868],"genre_scores_gemma":[0.763269,0.0003457274,0.23008178,0.00027104243,0.000079640355,0.00015809477,0.003877031,0.0005752454,0.0013424605],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9996019,0.000080105136,0.00001769376,0.00013553118,0.000105787,0.00005897487],"domain_scores_gemma":[0.9991416,0.00043131367,0.00012662521,0.00012321744,0.00011484692,0.000062421],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0012833256,0.00051330903,0.0006523401,0.00081002293,0.0002474713,0.00091734756,0.00048569488,0.00048978545,0.00075589813],"category_scores_gemma":[0.002123167,0.00038883986,0.00084336573,0.00087227364,0.00053627027,0.00064856885,0.0006603071,0.0009912169,0.0003545656],"study_design_candidate":"bench_or_experimental","study_design_consensus":"bench_or_experimental","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0005093605,0.00012891964,0.013488713,0.0003214695,0.00030222087,0.00016310326,0.00022184494,0.11981368,0.7597264,0.018711558,0.0029059725,0.08370679],"study_design_scores_gemma":[0.000018513285,0.000040404426,0.019675033,0.000011118511,0.000042596617,0.00007524061,0.000051806248,0.9265388,0.0323316,0.019764895,0.001405718,0.00004424239],"about_ca_topic_score_codex":0.0028643967,"about_ca_topic_score_gemma":0.006495272,"teacher_disagreement_score":0.0028643967,"about_ca_system_score_codex":0.0005052511,"about_ca_system_score_gemma":0.0008633623,"threshold_uncertainty_score":0.006787002},"labels":[],"label_agreement":null},{"id":"W4405995913","doi":"10.1038/s41588-024-01978-2","title":"The impact of common and rare genetic variants on bradyarrhythmia development","year":2025,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Cardiac electrophysiology and arrhythmias","field":"Medicine","cited_by":19,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Western University","funders":"Common Fund; National Institute of Neurological Disorders and Stroke; National Cancer Institute; NIH Office of the Director; National Human Genome Research Institute; National Institute on Drug Abuse; National Institutes of Health; National Institute of Mental Health; National Heart, Lung, and Blood Institute; Vetenskapsrådet; Knut och Alice Wallenbergs Stiftelse; National Institute on Aging; Hjärt-Lungfonden; American Heart Association; Hartstichting; U.S. Department of Veterans Affairs; Stiftelsen för Strategisk Forskning; Office of Research and Development; Fondation Leducq; European Commission; Sigrid Juséliuksen Säätiö","keywords":"Biology; Genetics; Computational biology; Evolutionary biology","score_opus":0.005103179761599704,"score_gpt":0.28258885306073095,"score_spread":0.27748567329913126,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4405995913","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99335563,0.0024331212,0.0023162633,0.000102313796,0.000016987387,0.0000073501783,0.0004898099,0.000027006976,0.0012517129],"genre_scores_gemma":[0.9984792,0.00036216993,0.0008042535,0.000034533175,0.00001942554,0.000003966313,0.0001732992,0.000010083001,0.00011303831],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99800354,0.00056794495,0.00017223177,0.00081989734,0.00027001527,0.00016624072],"domain_scores_gemma":[0.99669445,0.0019346435,0.00067939254,0.00028865619,0.00012954853,0.00027333878],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0013355007,0.00043480887,0.00046782792,0.0013312579,0.00029843833,0.00070427137,0.00032680228,0.0004949296,0.001744981],"category_scores_gemma":[0.003082398,0.00019492034,0.00067329156,0.0008792899,0.00061144785,0.00033477548,0.0007426204,0.00046422455,0.00011858098],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0007258132,0.0000439126,0.91962,0.0001161573,0.0011109497,0.0033426022,0.00027744222,0.001088673,0.041557662,0.0015285088,0.0002507541,0.03033756],"study_design_scores_gemma":[0.000020788606,0.00010425983,0.9922431,0.000022168115,0.00033309305,0.0027463124,0.0000692684,0.0010707112,0.001807943,0.0008500412,0.0007186009,0.000013736434],"about_ca_topic_score_codex":0.0014148625,"about_ca_topic_score_gemma":0.0029486988,"teacher_disagreement_score":0.001744981,"about_ca_system_score_codex":0.00019290429,"about_ca_system_score_gemma":0.00021118145,"threshold_uncertainty_score":0.007062912},"labels":[],"label_agreement":null},{"id":"W4406034886","doi":"10.1038/s41588-024-02014-z","title":"ZIC1 is a context-dependent medulloblastoma driver in the rhombic lip","year":2025,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Genomics and Chromatin Dynamics","field":"Biochemistry, Genetics and Molecular Biology","cited_by":12,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Princess Margaret Cancer Centre; McMaster University; McGill University; University of Calgary; University Health Network; University of Toronto; SickKids Foundation; Hospital for Sick Children","funders":"DOD Peer Reviewed Cancer Research Program; National Institute of Neurological Disorders and Stroke; Brain Tumour Research; Debreceni Egyetem; Hospital for Sick Children; National Cancer Institute; University of Toronto; Stand Up To Cancer; Genome British Columbia; Wellcome Trust; American Lebanese Syrian Associated Charities; Genome Canada; St. Jude Children's Research Hospital; Medical Research Council; Cancer Prevention and Research Institute of Texas; Government of Ontario; American Association for Cancer Research; Canadian Institutes of Health Research; Pediatric Brain Tumor Foundation; Government of Canada; Canadian Cancer Society Research Institute; National Institutes of Health; U.S. Department of Health and Human Services","keywords":"Medulloblastoma; Biology; Context (archaeology); Cancer research; Mutant; Genetics; Gene","score_opus":0.002976206457785871,"score_gpt":0.23212053328052065,"score_spread":0.22914432682273478,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4406034886","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9942463,0.00041958643,0.002874389,0.000066597284,0.000007140959,0.000020032357,0.00031844043,0.00013039078,0.0019172292],"genre_scores_gemma":[0.99581075,0.00022799593,0.0015556692,0.000016339282,0.0000019111112,0.000012555594,0.0003130636,0.000023708128,0.0020380425],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9998708,0.000010863056,0.000007451863,0.00002899999,0.000051404957,0.00003048043],"domain_scores_gemma":[0.9999361,0.00000798022,0.000025699464,0.000008484375,0.0000042022457,0.000017541848],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.000055172604,0.00024934375,0.00012602229,0.00037268584,0.00017863407,0.00020238708,0.0002090668,0.00016938265,0.0010363868],"category_scores_gemma":[0.000070525726,0.00019143824,0.00014953395,0.00015006703,0.00026069224,0.00009873428,0.0002848719,0.0004634075,0.0003541224],"study_design_candidate":"bench_or_experimental","study_design_consensus":"bench_or_experimental","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.000020299953,0.0000036374813,0.000359793,0.0000069645994,0.0000021512617,0.000052355586,0.0000070571336,0.000046641133,0.9988311,0.00016185836,0.000016593574,0.00049163407],"study_design_scores_gemma":[0.000011558408,0.00007226086,0.016986528,0.000004522411,0.000018766374,0.0007364456,0.000026506405,0.00122174,0.9777129,0.00006972333,0.0031354192,0.0000036327644],"about_ca_topic_score_codex":0.0029399206,"about_ca_topic_score_gemma":0.0069075827,"teacher_disagreement_score":0.0029399206,"about_ca_system_score_codex":0.0004623503,"about_ca_system_score_gemma":0.00027064118,"threshold_uncertainty_score":0.0058456063},"labels":[],"label_agreement":null},{"id":"W4406104380","doi":"10.1038/s41588-024-02028-7","title":"Emil Skamene (1941–2024)","year":2025,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Amino Acid Enzymes and Metabolism","field":"Biochemistry, Genetics and Molecular Biology","cited_by":0,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"McGill University Health Centre; McGill University","funders":"","keywords":"Biology; Computational biology; Evolutionary biology; Genetics","score_opus":0.003463439827439831,"score_gpt":0.2572036396734778,"score_spread":0.25374019984603796,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4406104380","genre_codex":"other","genre_gemma":"other","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"other","genre_consensus":"other","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.02481823,0.26717678,0.015311425,0.07749995,0.14661865,0.0002824457,0.003552064,0.0019026914,0.46283785],"genre_scores_gemma":[0.029524427,0.026954908,0.0019855206,0.0051031914,0.005602905,0.000050969997,0.0004486243,0.00016164112,0.93016773],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.9997644,0.000021645184,0.0000146826715,0.000097620046,0.00006887543,0.000032865883],"domain_scores_gemma":[0.99971765,0.000047570087,0.000033913006,0.000013941157,0.00007939686,0.000107430715],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00049331784,0.0009846288,0.00052041037,0.0011615797,0.0005926978,0.00057067076,0.00051664765,0.0010586426,0.097340904],"category_scores_gemma":[0.00075731275,0.0002092816,0.00022391453,0.00042321475,0.00043978673,0.00078061846,0.0010422842,0.0011702864,0.059384897],"study_design_candidate":"not_applicable","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.000565448,0.000090039546,0.0012085766,0.00050605077,0.000035886373,0.0011892748,0.000113897084,0.0005700386,0.009296728,0.010993253,0.45819166,0.51723915],"study_design_scores_gemma":[0.000006351446,0.000062948675,0.00072033796,0.0000334807,0.0000075798303,0.000737491,0.000011445039,0.000050268874,0.0017727735,0.0004157879,0.9961739,0.0000075788907],"about_ca_topic_score_codex":0.0010105824,"about_ca_topic_score_gemma":0.0011947232,"teacher_disagreement_score":0.097340904,"about_ca_system_score_codex":0.00063510437,"about_ca_system_score_gemma":0.0005227126,"threshold_uncertainty_score":0.32563782},"labels":[],"label_agreement":null},{"id":"W4406180041","doi":"10.1038/s41588-024-02032-x","title":"Tandem kinase proteins across the plant kingdom","year":2025,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Plant-Microbe Interactions and Immunity","field":"Agricultural and Biological Sciences","cited_by":24,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Saskatchewan","funders":"University of Haifa; United States-Israel Binational Science Foundation; National Institute of General Medical Sciences; United States - Israel Binational Agricultural Research and Development Fund; U.S. Department of Agriculture","keywords":"Biology; Effector; Protein kinase domain; Plant Immunity; Transmembrane protein; Cell biology; Computational biology; Plant protein; Immunity; Protein kinase A; Kinase; Genetics; Gene; Arabidopsis; Immune system; Receptor","score_opus":0.018495323399929695,"score_gpt":0.26374585538039086,"score_spread":0.24525053198046115,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4406180041","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.92764485,0.033272106,0.021231791,0.0014200044,0.00022458221,0.00003023913,0.0012477551,0.00041463302,0.014513926],"genre_scores_gemma":[0.9795434,0.008628464,0.0062922323,0.0003829758,0.00003420587,0.000011078205,0.0009192436,0.000060658094,0.0041277083],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9998273,0.000015426951,0.000016568152,0.000068331676,0.00003759402,0.00003483699],"domain_scores_gemma":[0.99974257,0.00004957019,0.000054919983,0.000032735785,0.000050191687,0.00006994639],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0002079168,0.00029492984,0.00033655294,0.0008039564,0.00032560434,0.0006996485,0.00029404458,0.00058503787,0.0015222229],"category_scores_gemma":[0.00026338117,0.00025929566,0.0002724137,0.00073933904,0.00030006372,0.0009084291,0.00084323226,0.0008926385,0.0007274668],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00044150825,0.00001733433,0.002706408,0.00026637543,0.000055682227,0.00047115053,0.00017375998,0.0003828208,0.953512,0.0044442653,0.00045273412,0.037075885],"study_design_scores_gemma":[0.00020993972,0.00045941633,0.25246727,0.00041465403,0.00076719484,0.017162822,0.0017044629,0.008024644,0.5055926,0.018841682,0.1941683,0.00018703454],"about_ca_topic_score_codex":0.000819597,"about_ca_topic_score_gemma":0.0012433182,"teacher_disagreement_score":0.0015222229,"about_ca_system_score_codex":0.00051953114,"about_ca_system_score_gemma":0.00027370287,"threshold_uncertainty_score":0.005092323},"labels":[],"label_agreement":null},{"id":"W4406232070","doi":"10.1038/s41588-024-02050-9","title":"Cell state-dependent allelic effects and contextual Mendelian randomization analysis for human brain phenotypes","year":2025,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Single-cell and spatial transcriptomics","field":"Biochemistry, Genetics and Molecular Biology","cited_by":26,"is_retracted":false,"has_abstract":true,"route_ca_aff":false,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"","funders":"Medical Research Council; Epilepsy Society; Imperial College London; Department of Health and Social Care; UK Dementia Research Institute; Engineering and Physical Sciences Research Council; UK Research and Innovation; Alzheimer Society; National Institute for Health and Care Research; Research Councils UK; Alzheimer's Society; Parkinson's UK; Katy Baggott Foundation","keywords":"Mendelian randomization; Biology; Phenotype; Allele; Disease; Genetics; Gene; Quantitative trait locus; Mendelian inheritance; Expression quantitative trait loci; Trait; Genetic variants; Single-nucleotide polymorphism; Genotype; Internal medicine; Medicine","score_opus":0.005064953713971898,"score_gpt":0.25040856883035206,"score_spread":0.24534361511638017,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4406232070","genre_codex":"methods","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":null,"domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.41437966,0.00044680902,0.5792383,0.00026767168,0.0000774561,0.0002902646,0.0022932738,0.0013414028,0.001665259],"genre_scores_gemma":[0.89903504,0.00008864507,0.09888139,0.0001445383,0.000024306197,0.0003229548,0.00091244694,0.00023202042,0.00035873038],"study_design_codex":"observational","study_design_gemma":"simulation_or_modeling","domain_scores_codex":[0.98539335,0.009467333,0.00044538075,0.0034852691,0.00089009054,0.00031857088],"domain_scores_gemma":[0.9879033,0.008839695,0.00075799174,0.0021758196,0.00017070102,0.00015257724],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.012541323,0.0004080828,0.0009343406,0.001060115,0.00044854687,0.0009626857,0.0009786652,0.0005322133,0.004378631],"category_scores_gemma":[0.023935584,0.00028642255,0.0015140993,0.0012620306,0.0011508951,0.00038943934,0.0009173423,0.0008764856,0.00029715535],"study_design_candidate":"simulation_or_modeling","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0064283735,0.00035482028,0.39999852,0.0009308299,0.00842742,0.0058080554,0.0018441853,0.0730596,0.14592005,0.1011541,0.0071101678,0.2489639],"study_design_scores_gemma":[0.0007110304,0.0011137554,0.42441255,0.00013913294,0.001981671,0.0044685397,0.0003096284,0.40117937,0.026070692,0.12602684,0.013323089,0.00026374255],"about_ca_topic_score_codex":0.0029246744,"about_ca_topic_score_gemma":0.0035734756,"teacher_disagreement_score":0.012541323,"about_ca_system_score_codex":0.00046616056,"about_ca_system_score_gemma":0.000736557,"threshold_uncertainty_score":0.066325665},"labels":[],"label_agreement":null},{"id":"W4406706759","doi":"10.1038/s41588-024-02054-5","title":"In vivo CRISPR–Cas9 genome editing in mice identifies genetic modifiers of somatic CAG repeat instability in Huntington’s disease","year":2025,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Genetic Neurodegenerative Diseases","field":"Neuroscience","cited_by":55,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Université Laval","funders":"National Institute of Neurological Disorders and Stroke; Dana-Farber/Harvard Cancer Center; CHDI Foundation; U.S. Department of Health and Human Services; National Institutes of Health; Harvard NeuroDiscovery Center; National Ataxia Foundation; Broad Institute; Pfizer; Huntington's Disease Society of America; Office of Extramural Research, National Institutes of Health; National Cancer Institute","keywords":"CRISPR; Biology; Genome editing; Somatic cell; Genetics; Huntington's disease; Cas9; Genome; Disease; Genome instability; Gene; DNA; DNA damage","score_opus":0.012381850662693213,"score_gpt":0.2804087256941455,"score_spread":0.2680268750314523,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4406706759","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.7843861,0.004253852,0.18588407,0.0010951448,0.0006531723,0.0008688263,0.0059388424,0.0043438706,0.012576143],"genre_scores_gemma":[0.888042,0.0031799453,0.08863767,0.00040882622,0.00006014094,0.00050319824,0.002993395,0.0005126133,0.015662193],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9995215,0.000042865566,0.00005934349,0.00016996982,0.00013824657,0.00006816735],"domain_scores_gemma":[0.9997429,0.000055105254,0.00008719911,0.00003442218,0.000018968663,0.00006137295],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0004683062,0.00090558885,0.0007041704,0.0007784924,0.00030687993,0.00060155324,0.0008841104,0.00095034286,0.0023075764],"category_scores_gemma":[0.00030106754,0.00051354343,0.0005091208,0.00022116404,0.0005988012,0.00029920673,0.0004227069,0.0015756831,0.0007182395],"study_design_candidate":"bench_or_experimental","study_design_consensus":"bench_or_experimental","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00008050355,0.000060892347,0.00010118732,0.00004186347,0.000016596601,0.00010952369,0.000024685954,0.00026107667,0.99630165,0.0005564483,0.00018362977,0.0022618405],"study_design_scores_gemma":[0.000050790764,0.00031844195,0.0015839468,0.00001985413,0.00004938642,0.0005103715,0.000017429113,0.0036395823,0.9850885,0.00023694271,0.008464857,0.000019775782],"about_ca_topic_score_codex":0.0010677757,"about_ca_topic_score_gemma":0.0029752818,"teacher_disagreement_score":0.0023075764,"about_ca_system_score_codex":0.000671053,"about_ca_system_score_gemma":0.00039040003,"threshold_uncertainty_score":0.0077195764},"labels":[],"label_agreement":null},{"id":"W4406805491","doi":"10.1038/s41588-024-02052-7","title":"Integrative proteogenomic analysis identifies COL6A3-derived endotrophin as a mediator of the effect of obesity on coronary artery disease","year":2025,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Atherosclerosis and Cardiovascular Diseases","field":"Immunology and Microbiology","cited_by":30,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"McGill University Health Centre; McGill University; McGill Genome Centre; University of Toronto; Jewish General Hospital","funders":"National Institute of Neurological Disorders and Stroke; NIH Office of the Director; National Human Genome Research Institute; National Institute of Mental Health; National Heart, Lung, and Blood Institute; Medical Research Council; Fonds de Recherche du Québec - Santé; National Institutes of Health; National Institute of Diabetes and Digestive and Kidney Diseases; Government of Canada; Fondation de l'Hôpital général juif; Ministry of Education, Culture, Sports, Science and Technology; National Institute on Drug Abuse; Novo Nordisk; Public Health Agency; National Cancer Institute; University of Bristol; European Commission; National Institute for Health and Care Research; TD Bank; King's College London; Jewish General Hospital; Canada Excellence Research Chairs, Government of Canada; Cancer Research UK; Wellcome Trust; Public Health Agency of Canada; McGill University; Canadian Institutes of Health Research; Compute Canada; Common Fund; Japan Society for the Promotion of Science; Novo Nordisk Fonden","keywords":"Mendelian randomization; Coronary artery disease; Disease; Bioinformatics; Obesity; Type 2 diabetes; Biology; Internal medicine; Diabetes mellitus; Medicine; Endocrinology; Cancer research; Gene; Genetics; Genotype; Genetic variants","score_opus":0.0028701471117077823,"score_gpt":0.22004269624682585,"score_spread":0.21717254913511808,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4406805491","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.97225994,0.0009913436,0.023038939,0.00021800285,0.000039367038,0.000023030754,0.0021805693,0.00020952059,0.0010392056],"genre_scores_gemma":[0.98323363,0.0006741482,0.012547206,0.00015173905,0.000014828586,0.000023338745,0.0022409705,0.0000858643,0.0010281263],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9998652,0.000022993756,0.000007145395,0.000045781344,0.000035872075,0.000023014862],"domain_scores_gemma":[0.99986684,0.000030120007,0.0000497082,0.000015413298,0.000010977098,0.00002690191],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00027660982,0.00038873628,0.00024106979,0.00044258602,0.0001687586,0.00029733215,0.00015780012,0.0002222667,0.0010112104],"category_scores_gemma":[0.00016171394,0.000110410954,0.000337824,0.00025877258,0.00020822848,0.000102341706,0.00033092257,0.00043782452,0.00019060205],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00012969639,0.000011192707,0.0019091273,0.000024614552,0.000025728166,0.00009734064,0.000009552617,0.00018432626,0.9951456,0.00019249145,0.00006427893,0.0022061062],"study_design_scores_gemma":[0.000060907663,0.00047558098,0.3907761,0.000035448542,0.0003711981,0.002275707,0.00012560493,0.016297573,0.57873106,0.0018007887,0.0090002185,0.00004989006],"about_ca_topic_score_codex":0.00051929377,"about_ca_topic_score_gemma":0.000953079,"teacher_disagreement_score":0.0010112104,"about_ca_system_score_codex":0.00018322973,"about_ca_system_score_gemma":0.00023442665,"threshold_uncertainty_score":0.0033828616},"labels":[],"label_agreement":null},{"id":"W4407107571","doi":"10.1038/s41588-024-02069-y","title":"A barley pan-transcriptome reveals layers of genotype-dependent transcriptional complexity","year":2025,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Wheat and Barley Genetics and Pathology","field":"Agricultural and Biological Sciences","cited_by":41,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Saskatchewan","funders":"Carlsbergfondet; Grains Research and Development Corporation; Biotechnology and Biological Sciences Research Council; Rural and Environment Science and Analytical Services Division; Genome Canada","keywords":"Biology; Transcriptome; RNA-Seq; Genome; Genetics; Computational biology; Gene; Gene expression profiling; Reference genome; Gene expression","score_opus":0.02193695844020681,"score_gpt":0.25737709690752353,"score_spread":0.2354401384673167,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4407107571","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.96489155,0.00042384668,0.02275284,0.00005152294,0.000012836857,0.00002224836,0.009867389,0.00045539203,0.0015223451],"genre_scores_gemma":[0.9614715,0.00037502163,0.020038718,0.00008216217,0.000009502757,0.00006167363,0.016268708,0.00022195003,0.0014707382],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9998362,0.000009436903,0.0000100287525,0.000094410134,0.00002761714,0.000022212169],"domain_scores_gemma":[0.9998123,0.000055713503,0.000037109196,0.000036969384,0.00003181057,0.000026105497],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00024198007,0.0002439391,0.00033103712,0.00035506167,0.00018925472,0.0005153467,0.0001308208,0.00015483997,0.00096949795],"category_scores_gemma":[0.00027243575,0.00018000774,0.00027041623,0.000604669,0.00016402273,0.00033538786,0.00038392883,0.00032013404,0.00026085586],"study_design_candidate":"bench_or_experimental","study_design_consensus":"bench_or_experimental","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00019212316,0.000009046416,0.008008569,0.000073731506,0.000022858718,0.00006759038,0.000099755685,0.0005347869,0.9840724,0.00020892535,0.00011201028,0.006598147],"study_design_scores_gemma":[0.000028143031,0.00025241653,0.7058667,0.000042525884,0.0001645384,0.0011420893,0.0003327805,0.010973451,0.26780778,0.0022974887,0.011042142,0.00004997192],"about_ca_topic_score_codex":0.00095312024,"about_ca_topic_score_gemma":0.0022418066,"teacher_disagreement_score":0.00096949795,"about_ca_system_score_codex":0.00030843334,"about_ca_system_score_gemma":0.0002191044,"threshold_uncertainty_score":0.0032433271},"labels":[],"label_agreement":null},{"id":"W4407342687","doi":"10.1038/s41588-025-02079-4","title":"The African Animal Breeding Network as a pathway towards genetic improvement of livestock","year":2025,"lang":"en","type":"review","venue":"Nature Genetics","topic":"Genetic and phenotypic traits in livestock","field":"Biochemistry, Genetics and Molecular Biology","cited_by":4,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Agriculture and Agri-Food Canada","funders":"Foreign, Commonwealth and Development Office; Bill and Melinda Gates Foundation; International Livestock Research Institute; Scotland’s Rural College; Biotechnology and Biological Sciences Research Council; Government of the United Kingdom","keywords":"Biology; Livestock; Biotechnology; Animal breeding; Genetics; Computational biology; Evolutionary biology; Ecology","score_opus":0.011586801682441852,"score_gpt":0.2802894306269212,"score_spread":0.2687026289444793,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4407342687","genre_codex":"review","genre_gemma":"review","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"review","genre_consensus":"review","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.0000680102,0.99752456,0.00018609285,0.00063800445,0.00036357163,0.000003612499,0.00001983219,0.0000069291514,0.0011894051],"genre_scores_gemma":[0.00046904906,0.99810636,0.00024321303,0.00028134158,0.00019576757,0.000004610273,0.000029446674,0.00000126945,0.0006689529],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.9998221,0.0000440739,0.00001910976,0.000027104761,0.00006282298,0.000024835112],"domain_scores_gemma":[0.99942327,0.00029655706,0.00008134509,0.000013262971,0.000115451614,0.00007011222],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.001088104,0.0008975048,0.00095179625,0.0021517242,0.00026868438,0.0011695448,0.000854925,0.0012836381,0.005683443],"category_scores_gemma":[0.0010266203,0.00018586406,0.00025498332,0.0026027123,0.00054342614,0.0012069759,0.00085704855,0.0017084634,0.0019866328],"study_design_candidate":"not_applicable","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00007115544,0.000047114547,0.00012824712,0.008198893,0.000042725864,0.00016117348,0.00003154578,0.0002643957,0.0011239271,0.0067608296,0.036391605,0.9467784],"study_design_scores_gemma":[0.000014096701,0.00004396324,0.0006155299,0.0031075554,0.00006042076,0.00042448624,0.00003888733,0.00006368803,0.00021938124,0.0016696355,0.99373347,0.00000895495],"about_ca_topic_score_codex":0.0012380795,"about_ca_topic_score_gemma":0.0023410043,"teacher_disagreement_score":0.005683443,"about_ca_system_score_codex":0.00080793997,"about_ca_system_score_gemma":0.0016012783,"threshold_uncertainty_score":0.019013047},"labels":[],"label_agreement":null},{"id":"W4407674910","doi":"10.1038/s41588-025-02087-4","title":"Large-scale genome-wide association analyses identify novel genetic loci and mechanisms in hypertrophic cardiomyopathy","year":2025,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Cardiomyopathy and Myosin Studies","field":"Medicine","cited_by":52,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Libin Cardiovascular Institute of Alberta; University of Calgary; McGill University; Western University; Hospital for Sick Children; Public Health Ontario; University Health Network; University of Toronto; Université de Montréal; Montreal Heart Institute","funders":"National Cancer Institute; NIH Office of the Director; National Institute of Mental Health; Canadian Institutes of Health Research; Amsterdam Cardiovascular Sciences, Amsterdam University Medical Centers; National Institutes of Health; National Human Genome Research Institute; Amsterdam University Medical Centers; UK Dementia Research Institute; Novo Nordisk Fonden; Institut de Cardiologie de Montréal; Institute of Psychiatry, Psychology and Neuroscience, King’s College London; Fondation Institut de Cardiologie de Montréal; ZonMw; Hartstichting; Common Fund; Deutsches Zentrum für Herz-Kreislaufforschung; Imperial College London; National Institute on Drug Abuse; Novo Nordisk; Fetal Medicine Foundation; National Institute for Health and Care Research; Medical Research Council; Israel Cancer Research Fund; Department of Health and Social Care; Fondation Leducq; King's College London; European Commission; National Institute of Neurological Disorders and Stroke; British Heart Foundation; Cancer Research UK; Wellcome Trust; Alzheimer's Society; National Heart, Lung, and Blood Institute; Maudsley Charity; U.S. Department of Health and Human Services","keywords":"Hypertrophic cardiomyopathy; Mendelian randomization; Genome-wide association study; Biology; Disease; Genetics; Genetic association; Cardiomyopathy; Biobank; Gene; Internal medicine; Single-nucleotide polymorphism; Genotype; Genetic variants; Heart failure; Medicine","score_opus":0.012758353220436336,"score_gpt":0.29710821631855877,"score_spread":0.28434986309812244,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4407674910","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9957557,0.002269227,0.0012338144,0.00017414328,0.000012229157,0.000008681056,0.00015402939,0.000015816833,0.0003764312],"genre_scores_gemma":[0.9983151,0.00045518897,0.00080992206,0.00006496456,0.000023159191,0.0000065526897,0.00015657302,0.000003970301,0.00016457327],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99950004,0.00023231887,0.00002908666,0.00011944868,0.00007003206,0.000049009857],"domain_scores_gemma":[0.99886084,0.0006198912,0.00027296226,0.00008529851,0.000043312557,0.00011770352],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0009981209,0.0003150489,0.00026814133,0.0007983144,0.0003564986,0.00042941413,0.00025503413,0.00046095313,0.001428509],"category_scores_gemma":[0.001804322,0.00014902024,0.0003840315,0.00066073553,0.00041152374,0.00014535747,0.0004969898,0.00035651558,0.00012389105],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0011322368,0.00009529481,0.9303922,0.00012641256,0.0010277489,0.0020634045,0.00044164146,0.0004940599,0.03938075,0.00036389325,0.00056601583,0.023916319],"study_design_scores_gemma":[0.000038161324,0.00010237952,0.9971079,0.000012582926,0.0001770036,0.00084150466,0.000088937326,0.00024302673,0.0008015245,0.00018457089,0.00039559664,0.0000069129937],"about_ca_topic_score_codex":0.0010455706,"about_ca_topic_score_gemma":0.0025551212,"teacher_disagreement_score":0.001428509,"about_ca_system_score_codex":0.0000962119,"about_ca_system_score_gemma":0.00016078359,"threshold_uncertainty_score":0.005278647},"labels":[],"label_agreement":null},{"id":"W4407675121","doi":"10.1038/s41588-025-02094-5","title":"Evaluation of polygenic scores for hypertrophic cardiomyopathy in the general population and across clinical settings","year":2025,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Cardiomyopathy and Myosin Studies","field":"Medicine","cited_by":40,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Université de Montréal; Montreal Heart Institute","funders":"Medical Research Council; Amsterdam Cardiovascular Sciences, Amsterdam University Medical Centers; Institute of Psychiatry, Psychology and Neuroscience, King’s College London; Fondation Leducq; European Commission; Rosetrees Trust; Department of Health and Social Care; Fetal Medicine Foundation; National Institute for Health and Care Research; Cancer Research UK; Gujarat Council on Science and Technology; Hartstichting; Maudsley Charity; British Heart Foundation; Wellcome Trust","keywords":"Hypertrophic cardiomyopathy; Genome-wide association study; Penetrance; Proband; Biology; Biobank; Population; Population stratification; Polygenic risk score; Genetic testing; Genetics; Internal medicine; Medicine; Genotype; Environmental health; Single-nucleotide polymorphism; Mutation; Phenotype; Gene","score_opus":0.034277889411730184,"score_gpt":0.405406577989445,"score_spread":0.37112868857771486,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4407675121","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9961099,0.0002823782,0.0016767365,0.0001392842,0.000016980153,0.000023928164,0.000841953,0.000023406303,0.00088531006],"genre_scores_gemma":[0.9980755,0.0000784136,0.0009021413,0.00003239899,0.00001672199,0.000020054296,0.0007175972,0.000007731015,0.00014929398],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9969495,0.0017085487,0.00020584173,0.00056101347,0.0004148243,0.00016029993],"domain_scores_gemma":[0.99224275,0.0032739963,0.002506943,0.0008883889,0.00049341854,0.0005945075],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.004644224,0.0007360988,0.0005403182,0.0020596322,0.0006272362,0.0009108346,0.00050220435,0.0005512205,0.0022921262],"category_scores_gemma":[0.015678596,0.00015468016,0.00088268414,0.0019309802,0.0005662269,0.0004831996,0.0013700944,0.0005535558,0.00028720137],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00019271567,0.000019055067,0.99418056,0.000013532958,0.00037412424,0.000107306834,0.000108525455,0.00024289306,0.00033125124,0.00013270897,0.0002593174,0.0040380154],"study_design_scores_gemma":[0.000018026121,0.00020132726,0.99713767,0.000009445079,0.00011591468,0.0003317252,0.0001335598,0.0013663371,0.00009329501,0.00032358008,0.00026079064,0.000008241618],"about_ca_topic_score_codex":0.0037889404,"about_ca_topic_score_gemma":0.0040684333,"teacher_disagreement_score":0.004644224,"about_ca_system_score_codex":0.0002507422,"about_ca_system_score_gemma":0.00032074132,"threshold_uncertainty_score":0.024561346},"labels":[],"label_agreement":null},{"id":"W4408119778","doi":"10.1038/s41588-025-02115-3","title":"Post-polyploidization centromere evolution in cotton","year":2025,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Research in Cotton Cultivation","field":"Agricultural and Biological Sciences","cited_by":27,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Ministry of Agriculture","funders":"","keywords":"Biology; Centromere; Genetics; Evolutionary biology; Chromosome; Gene","score_opus":0.009703895234464233,"score_gpt":0.27081693457481343,"score_spread":0.2611130393403492,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4408119778","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9986889,0.00019936464,0.00026910336,0.00002547376,0.0000016181201,0.0000020171024,0.00007372638,0.0000064818632,0.00073330547],"genre_scores_gemma":[0.9982139,0.00016884832,0.0002051879,0.000031440246,0.0000028413228,0.0000031488994,0.00017330752,0.0000117088,0.0011896442],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.99989045,0.000013016853,0.000007308293,0.000038042144,0.000026156631,0.00002513085],"domain_scores_gemma":[0.99960345,0.00010988676,0.000083900224,0.00004236132,0.000074282936,0.00008617907],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00026130662,0.00016366932,0.00020837305,0.00065124774,0.0004016089,0.0005136083,0.000384141,0.00042524608,0.0019756565],"category_scores_gemma":[0.00055978214,0.00014117383,0.00016481853,0.0006377107,0.00020859193,0.0004997749,0.00047584728,0.0003391863,0.0003424555],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00041140252,0.000031443025,0.025410771,0.0000371564,0.00002501662,0.00021061457,0.0002362148,0.00044122484,0.96073735,0.00044991777,0.00002926698,0.011979783],"study_design_scores_gemma":[0.000019617117,0.00018464314,0.9523189,0.00001046833,0.000032618595,0.00059730373,0.00038596228,0.0016561165,0.04187169,0.0003805542,0.0025194343,0.000022522494],"about_ca_topic_score_codex":0.00441699,"about_ca_topic_score_gemma":0.0076517374,"teacher_disagreement_score":0.00441699,"about_ca_system_score_codex":0.0008686354,"about_ca_system_score_gemma":0.00025117747,"threshold_uncertainty_score":0.008782566},"labels":[],"label_agreement":null},{"id":"W4408201413","doi":"10.1038/s41588-025-02074-9","title":"Sequencing in over 50,000 cases identifies coding and structural variation underlying atrial fibrillation risk","year":2025,"lang":"en","type":"review","venue":"Nature Genetics","topic":"Cardiomyopathy and Myosin Studies","field":"Medicine","cited_by":27,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"McGill University; University of Ottawa; University of Calgary; Providence Health Care; Hamilton Health Sciences; McMaster University; Université Laval; University of Saskatchewan; Université de Montréal; Population Health Research Institute; University of British Columbia; Western University","funders":"National Heart, Lung, and Blood Institute; National Institute of Biomedical Imaging and Bioengineering; Canadian Institutes of Health Research; National Institutes of Health; National Institute on Aging; Stiftelsen för Strategisk Forskning; Skånes universitetssjukhus; Schweizerische Herzstiftung; Vetenskapsrådet; Knut och Alice Wallenbergs Stiftelse; Lunds Universitet; U.S. Department of Veterans Affairs; Schweizerischer Nationalfonds zur Förderung der Wissenschaftlichen Forschung; Novo Nordisk; Hjärt-Lungfonden; Ministry of Education, Culture, Sports, Science and Technology; British Heart Foundation; National Institute of Mental Health; Tokyo Medical and Dental University; Universität Basel; Bundesministerium für Bildung und Forschung; National Science Foundation; Massachusetts General Hospital; Sarnoff Cardiovascular Research Foundation; Stiftelsen för Strategisk Forskning; Foundation for Cardiovascular Research; Novo Nordisk Fonden; Heart and Stroke Foundation of Canada; Hartstichting; Foundation for the National Institutes of Health; American Heart Association; Fondation Leducq; Amsterdam University Medical Centers; Deutsche Forschungsgemeinschaft; Svenska Sällskapet för Medicinsk Forskning; European Commission; Japan Society for the Promotion of Science; Deutsches Zentrum für Herz-Kreislaufforschung","keywords":"Biology; LMNA; Exome sequencing; Genetics; Atrial fibrillation; Exome; Transcriptome; Genetic architecture; Gene; Phenotype; Internal medicine; Bioinformatics; Medicine","score_opus":0.04875130194828344,"score_gpt":0.3706149516786016,"score_spread":0.32186364973031817,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4408201413","genre_codex":"review","genre_gemma":"review","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"review","genre_consensus":"review","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.00051179173,0.9973876,0.00043821265,0.000526172,0.00026154896,0.0000038131986,0.00007952503,0.000015015735,0.0007763462],"genre_scores_gemma":[0.0033351746,0.99423295,0.00071284256,0.00059860206,0.00048033777,0.0000070760548,0.00018443544,0.0000041976887,0.00044431604],"study_design_codex":"design_other","study_design_gemma":"observational","domain_scores_codex":[0.9997391,0.0000414584,0.000051794792,0.000076770135,0.000070108166,0.00002072077],"domain_scores_gemma":[0.9992267,0.0005441253,0.000077800694,0.00001931868,0.00009645651,0.00003562254],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0008911828,0.00076180696,0.0011209747,0.0015408545,0.00011084189,0.0005648354,0.00066023035,0.001003013,0.0015322734],"category_scores_gemma":[0.0013993863,0.00020880505,0.00050633156,0.0012176237,0.00033249808,0.00044187103,0.000426618,0.00090548873,0.0007086192],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00009313852,0.00002057026,0.0020169693,0.0060502766,0.0003159176,0.00052402884,0.000035746896,0.00022169913,0.0017759779,0.0011984605,0.017651122,0.97009605],"study_design_scores_gemma":[0.0001318876,0.00018461134,0.025640044,0.016734919,0.0025850697,0.010484991,0.00013901135,0.0004591456,0.0017073994,0.0063178455,0.93552744,0.000087678214],"about_ca_topic_score_codex":0.0010059553,"about_ca_topic_score_gemma":0.0015961386,"teacher_disagreement_score":0.0015408545,"about_ca_system_score_codex":0.0002759029,"about_ca_system_score_gemma":0.0008057945,"threshold_uncertainty_score":0.0051259995},"labels":[],"label_agreement":null},{"id":"W4408243472","doi":"10.1038/s41588-024-02064-3","title":"Genome-wide association study meta-analysis provides insights into the etiology of heart failure and its subtypes","year":2025,"lang":"en","type":"review","venue":"Nature Genetics","topic":"Genetic Associations and Epidemiology","field":"Biochemistry, Genetics and Molecular Biology","cited_by":41,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"McMaster University; University of Ottawa; Thrombosis and Atherosclerosis Research Institute; Population Health Research Institute; Université de Montréal; Montreal Heart Institute","funders":"National Institute on Aging; British Heart Foundation; National Heart, Lung, and Blood Institute; National Institute for Health and Care Research","keywords":"Biology; Genome-wide association study; Etiology; Heart failure; Genetics; Meta-analysis; Genetic association; Computational biology; Association (psychology); Bioinformatics; Gene; Internal medicine; Single-nucleotide polymorphism; Genotype; Medicine","score_opus":0.024013074656895565,"score_gpt":0.3240964619502271,"score_spread":0.30008338729333156,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4408243472","genre_codex":"review","genre_gemma":"review","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"review","genre_consensus":"review","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.00027575612,0.9981951,0.00048674262,0.0004878943,0.00012617452,0.000005125784,0.00011606882,0.000012591565,0.00029460038],"genre_scores_gemma":[0.005106904,0.9931345,0.0006657558,0.00037320275,0.0003208278,0.000015440024,0.00019970429,0.000008576908,0.00017510806],"study_design_codex":"design_other","study_design_gemma":"meta_analysis","domain_scores_codex":[0.9989108,0.00047138712,0.00012334193,0.0002448161,0.00020083018,0.000048802387],"domain_scores_gemma":[0.9950545,0.004048421,0.00029774904,0.00014294659,0.00033730493,0.00011900679],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0033042294,0.0014770293,0.0046320898,0.003199267,0.00017436202,0.0012395149,0.0011678048,0.0013271847,0.0035041294],"category_scores_gemma":[0.0065961364,0.00042806088,0.0031824487,0.004070677,0.00043222276,0.00068328227,0.000799004,0.0019306227,0.000766119],"study_design_candidate":"meta_analysis","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0008470903,0.00004859304,0.009364723,0.05937748,0.032387137,0.0003540138,0.000061249055,0.001969461,0.00074535265,0.0041901744,0.028280431,0.8623742],"study_design_scores_gemma":[0.0008528757,0.000863596,0.07837548,0.051766593,0.14754859,0.0054734484,0.0002530069,0.0036152056,0.0020093806,0.035684537,0.673231,0.00032630368],"about_ca_topic_score_codex":0.0017235769,"about_ca_topic_score_gemma":0.0034487005,"teacher_disagreement_score":0.0046320898,"about_ca_system_score_codex":0.0007381049,"about_ca_system_score_gemma":0.001537458,"threshold_uncertainty_score":0.017474651},"labels":[],"label_agreement":null},{"id":"W4408243820","doi":"10.1038/s41588-024-02072-3","title":"Meta-analysis of genome-wide associations and polygenic risk prediction for atrial fibrillation in more than 180,000 cases","year":2025,"lang":"en","type":"review","venue":"Nature Genetics","topic":"Genetic Associations and Epidemiology","field":"Biochemistry, Genetics and Molecular Biology","cited_by":45,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Université Laval; McMaster University; Population Health Research Institute","funders":"Common Fund; National Center for Research Resources; National Institute of Neurological Disorders and Stroke; National Center for Advancing Translational Sciences; National Human Genome Research Institute; National Institute on Drug Abuse; National Institute of Diabetes and Digestive and Kidney Diseases; NIH Office of the Director; National Institute of Mental Health; National Heart, Lung, and Blood Institute; National Institute on Aging; National Cancer Institute; National Institutes of Health; Office of Research and Development; U.S. Department of Veterans Affairs","keywords":"Biology; Atrial fibrillation; Genome-wide association study; Polygenic risk score; Multifactorial Inheritance; Computational biology; Genome; Internal medicine; Genetics; Bioinformatics; Single-nucleotide polymorphism; Gene; Medicine; Genotype","score_opus":0.04293565617754762,"score_gpt":0.3494148041792859,"score_spread":0.30647914800173826,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4408243820","genre_codex":"review","genre_gemma":"review","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"review","genre_consensus":"review","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.000665523,0.9983613,0.00032714652,0.00022742504,0.00010094852,0.000006487182,0.00017012148,0.000010462908,0.00013050223],"genre_scores_gemma":[0.009977233,0.9873116,0.0010736937,0.0005534944,0.00041360216,0.000025278314,0.0004552962,0.00000910713,0.00018072018],"study_design_codex":"design_other","study_design_gemma":"meta_analysis","domain_scores_codex":[0.99865854,0.0005284238,0.0002765685,0.0002680691,0.00021078705,0.000057552377],"domain_scores_gemma":[0.9959002,0.0032920446,0.0003609755,0.00013543658,0.00024662117,0.000064626576],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.004409548,0.0013116933,0.0047459947,0.0016176368,0.00014489886,0.0010417491,0.0013226507,0.0011126264,0.002013815],"category_scores_gemma":[0.005834548,0.000527668,0.0053016865,0.0028769893,0.00022412962,0.00055374316,0.0007749415,0.001222868,0.0003716369],"study_design_candidate":"meta_analysis","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0024688954,0.00009066002,0.017275652,0.111091845,0.13172987,0.0005533664,0.00009807661,0.0013489401,0.0011359778,0.0013435067,0.0198208,0.71304244],"study_design_scores_gemma":[0.0021801367,0.0012493243,0.12830143,0.050931547,0.5267162,0.0043577165,0.00022589206,0.0020525833,0.0016357092,0.011437766,0.27052018,0.00039159931],"about_ca_topic_score_codex":0.0020468477,"about_ca_topic_score_gemma":0.005355254,"teacher_disagreement_score":0.0047459947,"about_ca_system_score_codex":0.0004371435,"about_ca_system_score_gemma":0.0014441046,"threshold_uncertainty_score":0.023320198},"labels":[],"label_agreement":null},{"id":"W4408275945","doi":"10.1038/s41588-025-02123-3","title":"An enhanced framework for local genetic correlation analysis","year":2025,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Genetic Associations and Epidemiology","field":"Biochemistry, Genetics and Molecular Biology","cited_by":11,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Centre for Global Health Research","funders":"National Natural Science Foundation of China-Yunnan Joint Fund; Vetenskapsrådet; Ministry of Science and Technology of the People's Republic of China; National Natural Science Foundation of China","keywords":"Biology; Computational biology; Correlation; Genetics; Evolutionary biology","score_opus":0.004787657498750899,"score_gpt":0.30310136689913114,"score_spread":0.29831370940038027,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4408275945","genre_codex":"methods","genre_gemma":"methods","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"methods","genre_consensus":"methods","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.0005333679,0.000050663515,0.9985678,0.000037054346,0.000009138477,0.000014232349,0.00007424277,0.00046377673,0.00024966605],"genre_scores_gemma":[0.04701923,0.00018441572,0.9497302,0.00011580904,0.00009260977,0.0002136803,0.0004980806,0.00047181823,0.0016741332],"study_design_codex":"theoretical_or_conceptual","study_design_gemma":"simulation_or_modeling","domain_scores_codex":[0.9962196,0.0020059526,0.00022320183,0.00059297995,0.0007904586,0.00016787372],"domain_scores_gemma":[0.9903286,0.0060858545,0.00034549215,0.0019155862,0.0010526123,0.0002717891],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0053805546,0.001036937,0.0021406433,0.002809815,0.0011225706,0.0025778138,0.0033441081,0.0011064506,0.0075031626],"category_scores_gemma":[0.019938482,0.00090979895,0.002414871,0.0032669585,0.0010791102,0.0023699214,0.0050944914,0.0024883742,0.002889003],"study_design_candidate":"simulation_or_modeling","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00033258626,0.00024058404,0.006701971,0.0003715051,0.00059448386,0.0010706634,0.0005683071,0.18486303,0.007996729,0.43272546,0.010287909,0.35424668],"study_design_scores_gemma":[0.000050118644,0.000043241827,0.0007567766,0.000032844204,0.00010360628,0.00032192434,0.0000477285,0.74429655,0.001054855,0.24486767,0.008380366,0.00004426964],"about_ca_topic_score_codex":0.0057439064,"about_ca_topic_score_gemma":0.007849202,"teacher_disagreement_score":0.0075031626,"about_ca_system_score_codex":0.00065560825,"about_ca_system_score_gemma":0.0020167294,"threshold_uncertainty_score":0.028455436},"labels":[],"label_agreement":null},{"id":"W4408341828","doi":"10.1038/s41588-025-02077-6","title":"Alterations in PD-L1 succinylation shape anti-tumor immune responses in melanoma","year":2025,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Immune cells in cancer","field":"Immunology and Microbiology","cited_by":72,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"SKiN Health","funders":"Key Programme; National Natural Science Foundation of China","keywords":"Succinylation; Biology; Immune system; Melanoma; Immunology; Cancer research; Tumor immunology; Immunotherapy; Genetics; Amino acid","score_opus":0.006841137198446976,"score_gpt":0.2707206123060388,"score_spread":0.2638794751075918,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4408341828","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.993644,0.0021709844,0.0020155858,0.00010231363,0.00002530996,0.0000189986,0.000971436,0.000067911744,0.0009834134],"genre_scores_gemma":[0.99697757,0.00068677904,0.000745903,0.000081616585,0.0000052117307,0.0000227981,0.00041474716,0.000015038046,0.0010502654],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9999118,0.000010100511,0.000005557812,0.00003275863,0.00001826411,0.000021485806],"domain_scores_gemma":[0.99995136,0.0000046750592,0.000016017768,0.000004025754,0.00001008678,0.0000138564055],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.000094363495,0.00015842232,0.00017994219,0.00021868844,0.00011744889,0.00033877674,0.000065259446,0.00021137264,0.00090962136],"category_scores_gemma":[0.00010575662,0.00013802345,0.0002185265,0.00015684232,0.00013946256,0.00020726185,0.0001444443,0.0004963992,0.00030113355],"study_design_candidate":"bench_or_experimental","study_design_consensus":"bench_or_experimental","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00045881493,0.000023675193,0.0027279416,0.000038834143,0.000011312951,0.000027286645,0.000023824885,0.00015241407,0.992861,0.00006342914,0.00007997338,0.0035315286],"study_design_scores_gemma":[0.000089456145,0.0008961356,0.18492527,0.000025245217,0.00008030422,0.0004338093,0.00032971893,0.0058374144,0.79912245,0.00062437955,0.0076078093,0.000027980279],"about_ca_topic_score_codex":0.00048773436,"about_ca_topic_score_gemma":0.00086200173,"teacher_disagreement_score":0.00090962136,"about_ca_system_score_codex":0.00037368448,"about_ca_system_score_gemma":0.00014722708,"threshold_uncertainty_score":0.003042996},"labels":[],"label_agreement":null},{"id":"W4408502235","doi":"10.1038/s41588-025-02121-5","title":"The Farm Animal Genotype–Tissue Expression (FarmGTEx) Project","year":2025,"lang":"en","type":"review","venue":"Nature Genetics","topic":"Genetic and phenotypic traits in livestock","field":"Biochemistry, Genetics and Molecular Biology","cited_by":43,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Alberta; Agriculture and Agri-Food Canada; McGill University; University of British Columbia","funders":"National Human Genome Research Institute; National Institute of Food and Agriculture; Aarhus Universitet; Directorate for Biological Sciences; Carnegie Mellon University; U.S. Department of Agriculture","keywords":"Biology; Genotype; Expression (computer science); Genetics; Computational biology; Gene","score_opus":0.014610663037354279,"score_gpt":0.32689005255089565,"score_spread":0.3122793895135414,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4408502235","genre_codex":"review","genre_gemma":"review","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"review","genre_consensus":"review","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.00040017982,0.9861624,0.0018411492,0.0019296312,0.0011629447,0.000028272889,0.00028421212,0.00009487611,0.008096457],"genre_scores_gemma":[0.0020816615,0.98389095,0.0018621772,0.0012927236,0.00044118898,0.000055499193,0.00064440176,0.000025615314,0.009705862],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.9997702,0.000044391272,0.000016631811,0.00004175212,0.00009366263,0.00003330449],"domain_scores_gemma":[0.9996468,0.00013129259,0.00004423253,0.000017931736,0.00007895294,0.00008078071],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0012740502,0.0009244856,0.0010863981,0.0011807493,0.0001756114,0.0010362708,0.0010449447,0.0013057913,0.006531476],"category_scores_gemma":[0.00059193256,0.00022616402,0.00028424518,0.0013362094,0.0005259595,0.00065334805,0.0007572493,0.001967356,0.0038930967],"study_design_candidate":"not_applicable","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0001876379,0.00007481964,0.00012199878,0.0029975944,0.000044668668,0.0001957085,0.000020086183,0.00027307507,0.0039698156,0.0061279885,0.08757682,0.8984097],"study_design_scores_gemma":[0.000032846874,0.000046634093,0.0004693217,0.0006421726,0.00003837988,0.00035090168,0.000008677217,0.000045686338,0.00076935877,0.0008313089,0.9967573,0.000007389049],"about_ca_topic_score_codex":0.0011574031,"about_ca_topic_score_gemma":0.0016568075,"teacher_disagreement_score":0.006531476,"about_ca_system_score_codex":0.0007388069,"about_ca_system_score_gemma":0.0013076832,"threshold_uncertainty_score":0.02184999},"labels":[],"label_agreement":null},{"id":"W4408771397","doi":"10.1038/s41588-025-02128-y","title":"The landscape of N6-methyladenosine in localized primary prostate cancer","year":2025,"lang":"en","type":"article","venue":"Nature Genetics","topic":"RNA modifications and cancer","field":"Biochemistry, Genetics and Molecular Biology","cited_by":19,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Université Laval; Vector Institute; Sunnybrook Hospital; University Health Network; University of Toronto; Princess Margaret Cancer Centre","funders":"CIHR Skin Research Training Centre; National Cancer Institute; National Human Genome Research Institute; Government of Canada","keywords":"Biology; Germline; Prostate cancer; DNA methylation; Germline mutation; Transcriptome; Metastasis; Somatic cell; Genetics; microRNA; RNA; Cancer research; Gene; Cancer; Gene expression; Mutation","score_opus":0.0038309046306845068,"score_gpt":0.26905380534956835,"score_spread":0.2652229007188838,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4408771397","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9790429,0.011803362,0.0012433453,0.0005942644,0.000019108556,0.0000074666655,0.00045231485,0.000088053064,0.0067491704],"genre_scores_gemma":[0.99681526,0.0013401703,0.0002063781,0.000058202513,0.0000085819565,0.000003254164,0.00011439664,0.000009503238,0.0014443165],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.99992466,0.000010471959,0.0000024273834,0.000021316884,0.000018663231,0.000022478858],"domain_scores_gemma":[0.9999205,0.000015668958,0.000017153308,0.0000052642945,0.000017996479,0.00002335296],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.000120678524,0.00010900995,0.00018577157,0.00030378153,0.00025286135,0.00049514405,0.00016574979,0.00020318835,0.0023206882],"category_scores_gemma":[0.00018086798,0.00013905276,0.00011232435,0.000260024,0.00020736779,0.00018829964,0.00017664205,0.00018408975,0.00024082765],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00051107537,0.000027735312,0.016094169,0.00011604687,0.000040609633,0.00038050086,0.00013782326,0.0012305307,0.9608449,0.0020622478,0.00056918856,0.017985137],"study_design_scores_gemma":[0.000038738868,0.0012848479,0.4321586,0.000048040147,0.00018271594,0.0039948183,0.0010834036,0.009036896,0.5110694,0.0057196887,0.035332862,0.000049964143],"about_ca_topic_score_codex":0.0029187931,"about_ca_topic_score_gemma":0.0055231405,"teacher_disagreement_score":0.0029187931,"about_ca_system_score_codex":0.00065462984,"about_ca_system_score_gemma":0.00027540277,"threshold_uncertainty_score":0.0077634454},"labels":[],"label_agreement":null},{"id":"W4408996073","doi":"10.1038/s41588-025-02124-2","title":"Causal machine learning for single-cell genomics","year":2025,"lang":"en","type":"review","venue":"Nature Genetics","topic":"Single-cell and spatial transcriptomics","field":"Biochemistry, Genetics and Molecular Biology","cited_by":28,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Canadian Institute for Advanced Research; Université de Montréal; Mila - Quebec Artificial Intelligence Institute","funders":"","keywords":"Interpretability; Genomics; Biology; Computational biology; Functional genomics; Systems biology; Generalization; Perspective (graphical); Machine learning; Computer science; Artificial intelligence; Genome; Genetics; Gene","score_opus":0.020292823832619756,"score_gpt":0.2820527375435668,"score_spread":0.26175991371094703,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4408996073","genre_codex":"review","genre_gemma":"review","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"review","genre_consensus":"review","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.00013205089,0.97915775,0.014976461,0.00229658,0.0007995146,0.000007589233,0.00006541782,0.00006441756,0.0025002006],"genre_scores_gemma":[0.005057589,0.9817479,0.0071150237,0.0012933452,0.002224026,0.000027444648,0.0001353172,0.000025997404,0.0023732493],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.9996705,0.000107641725,0.000023277002,0.00007879452,0.00009953343,0.000020375766],"domain_scores_gemma":[0.9983241,0.0013460141,0.00006304594,0.000077524826,0.00014577733,0.00004354011],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0015526393,0.000991563,0.0014093374,0.0013102669,0.00027413195,0.0012007516,0.0016531361,0.0020160128,0.0048874714],"category_scores_gemma":[0.0029063635,0.0004817482,0.00055994675,0.0017955278,0.001952468,0.0019781308,0.000966922,0.0032962975,0.0018195861],"study_design_candidate":"not_applicable","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00005806676,0.00006184535,0.00018913057,0.005797289,0.00016542878,0.00014114752,0.000027027663,0.0046636485,0.0007918908,0.11742226,0.05367238,0.8170099],"study_design_scores_gemma":[0.000043868382,0.000055991615,0.0006062575,0.0023766442,0.00011061205,0.00062648905,0.000019318302,0.005567538,0.0011816146,0.22799832,0.761351,0.0000623599],"about_ca_topic_score_codex":0.0018850727,"about_ca_topic_score_gemma":0.0017555526,"teacher_disagreement_score":0.0048874714,"about_ca_system_score_codex":0.0014128038,"about_ca_system_score_gemma":0.0013580532,"threshold_uncertainty_score":0.01635021},"labels":[],"label_agreement":null},{"id":"W4409040137","doi":"10.1038/s41588-025-02139-9","title":"Spatially resolved transcriptomic analysis of the adult human prostate","year":2025,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Molecular Biology Techniques and Applications","field":"Biochemistry, Genetics and Molecular Biology","cited_by":14,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Princess Margaret Cancer Centre; University of Toronto; University Health Network","funders":"","keywords":"Biology; Transcriptome; Computational biology; Prostate; Evolutionary biology; Genetics; Gene; Gene expression; Cancer","score_opus":0.0035724099722687364,"score_gpt":0.2715826824015596,"score_spread":0.2680102724292909,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4409040137","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9787138,0.004659764,0.0090286415,0.00013940418,0.000023119579,0.000025993919,0.0036532918,0.00010343261,0.0036524802],"genre_scores_gemma":[0.98588645,0.0020239793,0.0051185996,0.00010054059,0.0000147734145,0.000024985324,0.0024240464,0.000038547227,0.0043680677],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.99995434,0.0000039517245,0.0000016973121,0.000013895989,0.000013246538,0.000012963558],"domain_scores_gemma":[0.9999571,0.000010046554,0.0000070135316,0.0000049332616,0.000011299178,0.000009526929],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.000065072396,0.000095426105,0.00014165224,0.00033314058,0.00016555961,0.00026404017,0.00010844883,0.00013741018,0.0010842651],"category_scores_gemma":[0.00006948579,0.00012125909,0.00017606963,0.00028461235,0.00014797752,0.00009575581,0.00016570585,0.00023088284,0.00031133776],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00007835623,0.0000036600754,0.00087653653,0.000028598786,0.000005658152,0.00007392375,0.00002376172,0.0000736914,0.9968137,0.00008805409,0.000049830956,0.0018842063],"study_design_scores_gemma":[0.000016215288,0.00027548106,0.30897686,0.00001676685,0.00008328234,0.0020692858,0.0005921407,0.001809148,0.67288506,0.0002731327,0.012984844,0.00001780711],"about_ca_topic_score_codex":0.0025315592,"about_ca_topic_score_gemma":0.004404105,"teacher_disagreement_score":0.0025315592,"about_ca_system_score_codex":0.000119907236,"about_ca_system_score_gemma":0.0002232405,"threshold_uncertainty_score":0.0050337315},"labels":[],"label_agreement":null},{"id":"W4409148791","doi":"10.1038/s41588-025-02127-z","title":"Psychiatric genetics in the diverse landscape of Latin American populations","year":2025,"lang":"en","type":"review","venue":"Nature Genetics","topic":"Genetic Associations and Epidemiology","field":"Biochemistry, Genetics and Molecular Biology","cited_by":17,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Child, Adolescent and Family Mental Health; Alberta Health Services; University of British Columbia","funders":"National Human Genome Research Institute; National Institute on Drug Abuse; National Institute on Aging; U.S. Department of Health and Human Services; Vetenskapsrådet; National Institute of Mental Health","keywords":"Psychiatric genetics; Genome-wide association study; Latin Americans; Genomics; Genetic association; Biology; Psychiatry; Evolutionary biology; Genetics; Medicine; Genome; Schizophrenia (object-oriented programming); Single-nucleotide polymorphism; Political science; Genotype; Gene","score_opus":0.02533954571076252,"score_gpt":0.3467806992258714,"score_spread":0.3214411535151089,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4409148791","genre_codex":"review","genre_gemma":"review","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"review","genre_consensus":"review","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.000037597823,0.9986029,0.00009727732,0.0006999657,0.00019440024,0.0000012860729,0.000017763396,0.0000038425087,0.0003450001],"genre_scores_gemma":[0.00025788468,0.9985892,0.00012501758,0.00030361593,0.00048179156,0.000002561996,0.000023422126,9.749126e-7,0.00021537395],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.9997379,0.00007548417,0.000036836213,0.00005856051,0.00007051913,0.000020650261],"domain_scores_gemma":[0.99880624,0.0007889437,0.00011786423,0.00002797455,0.0001808504,0.000078108],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.001322911,0.0010049628,0.0015723925,0.0023598603,0.00026213683,0.0013613579,0.0011662446,0.0017893184,0.0029760865],"category_scores_gemma":[0.0023122632,0.00030748206,0.00045661026,0.0032598455,0.0009315561,0.0010691548,0.0010381606,0.0020699224,0.00095848355],"study_design_candidate":"not_applicable","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00007511342,0.000040491956,0.0009647359,0.007973844,0.00015571005,0.00021153716,0.00004792017,0.00031719517,0.00031098694,0.004735152,0.05057215,0.9345951],"study_design_scores_gemma":[0.000042258933,0.000055298104,0.006375392,0.013138686,0.00041509268,0.0018366777,0.00012804137,0.00022055795,0.00014351282,0.008357356,0.9692431,0.00004405021],"about_ca_topic_score_codex":0.0072188,"about_ca_topic_score_gemma":0.013953874,"teacher_disagreement_score":0.0072188,"about_ca_system_score_codex":0.0011686278,"about_ca_system_score_gemma":0.0020922378,"threshold_uncertainty_score":0.014353573},"labels":[],"label_agreement":null},{"id":"W4409269443","doi":"10.1038/s41588-025-02155-9","title":"Genetic regulation of gene expression across multiple tissues in chickens","year":2025,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Genetic Mapping and Diversity in Plants and Animals","field":"Biochemistry, Genetics and Molecular Biology","cited_by":54,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"McGill University","funders":"Agricultural Research Service; National Natural Science Foundation of China; U.S. Department of Agriculture","keywords":"Biology; Gene; Gene expression; Genetics; Regulation of gene expression; Expression (computer science); Computational biology; Evolutionary biology","score_opus":0.006894845628296127,"score_gpt":0.26173289240871905,"score_spread":0.25483804678042293,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4409269443","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9972114,0.00050152326,0.0011509607,0.000035883684,0.0000077230925,0.0000048717293,0.00013000779,0.000022478449,0.0009351053],"genre_scores_gemma":[0.9955486,0.00022715425,0.0012341385,0.000044538498,0.0000051147395,0.000014178265,0.00019349503,0.000050815495,0.0026819697],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99968123,0.000028703467,0.00002039564,0.00015820729,0.000055236702,0.000056228146],"domain_scores_gemma":[0.99939203,0.00019562217,0.0001423267,0.000050585215,0.000080642145,0.00013877246],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00013317584,0.00031425874,0.00034150173,0.0009912777,0.00037525952,0.00056188536,0.0004421504,0.000400945,0.0007075506],"category_scores_gemma":[0.00023435535,0.00060324004,0.00027794985,0.00026308576,0.0005912173,0.00029693954,0.00046981926,0.0006799712,0.00018837795],"study_design_candidate":"bench_or_experimental","study_design_consensus":"bench_or_experimental","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00010938165,0.0000047751255,0.0006710968,0.000010770316,0.0000045749707,0.000039750856,0.00002995086,0.00005704869,0.99850214,0.00008304297,0.0000067936853,0.00048075197],"study_design_scores_gemma":[0.00007223134,0.00043543256,0.28912145,0.000037438338,0.00009006756,0.00077995117,0.00034342668,0.0024652283,0.70460886,0.00033264494,0.0016771668,0.00003610787],"about_ca_topic_score_codex":0.0038579537,"about_ca_topic_score_gemma":0.006785563,"teacher_disagreement_score":0.0038579537,"about_ca_system_score_codex":0.0007293108,"about_ca_system_score_gemma":0.00023063952,"threshold_uncertainty_score":0.0076709986},"labels":[],"label_agreement":null},{"id":"W4410242339","doi":"10.1038/s41588-025-02168-4","title":"Deciphering the longitudinal trajectories of glioblastoma ecosystems by integrative single-cell genomics","year":2025,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Single-cell and spatial transcriptomics","field":"Biochemistry, Genetics and Molecular Biology","cited_by":54,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Toronto; St. Michael's Hospital","funders":"National Institute of Neurological Disorders and Stroke; Japan Society for the Promotion of Science; University of Texas MD Anderson Cancer Center; National Cancer Institute; Conquer Cancer Foundation; National Institutes of Health; Servier; Fonds National de la Recherche Luxembourg; Council for Higher Education","keywords":"Biology; Glioblastoma; Genomics; Computational biology; Ecosystem; Evolutionary biology; Genetics; Ecology; Gene; Genome; Cancer research","score_opus":0.006311846555488069,"score_gpt":0.2256578939789791,"score_spread":0.219346047423491,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4410242339","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9846207,0.0011078048,0.011205319,0.00012947839,0.0000136715025,0.000021691998,0.0020726658,0.000091146256,0.00073747657],"genre_scores_gemma":[0.9895242,0.0006564171,0.0067815986,0.000114933784,0.000013100533,0.00003326371,0.0024719117,0.00005341534,0.00035112817],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99983823,0.000025189041,0.000008691944,0.00006469515,0.000030769977,0.000032354965],"domain_scores_gemma":[0.9997434,0.00006119449,0.000082653896,0.000036822858,0.000047684232,0.00002821788],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00037611905,0.00017114787,0.0004035204,0.000483981,0.00023246887,0.0007078899,0.00019883587,0.00021572819,0.000385534],"category_scores_gemma":[0.0006381879,0.0001553847,0.00027111507,0.00061813404,0.0003272946,0.00045340956,0.00042702976,0.00036464655,0.00019344894],"study_design_candidate":"bench_or_experimental","study_design_consensus":"bench_or_experimental","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00031745766,0.000072651805,0.34033316,0.00024597955,0.0003304236,0.0002219691,0.000879445,0.0056607327,0.602349,0.0017949903,0.00069881254,0.047095302],"study_design_scores_gemma":[0.000008501942,0.00022517402,0.9157902,0.00004159846,0.0001827275,0.00046935896,0.0011958577,0.020696668,0.051003147,0.004279557,0.0060583213,0.000048826765],"about_ca_topic_score_codex":0.0029436718,"about_ca_topic_score_gemma":0.0068841362,"teacher_disagreement_score":0.0029436718,"about_ca_system_score_codex":0.0004208343,"about_ca_system_score_gemma":0.0003991724,"threshold_uncertainty_score":0.005853057},"labels":[],"label_agreement":null},{"id":"W4410242531","doi":"10.1038/s41588-025-02167-5","title":"The multilayered transcriptional architecture of glioblastoma ecosystems","year":2025,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Single-cell and spatial transcriptomics","field":"Biochemistry, Genetics and Molecular Biology","cited_by":84,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Toronto; St. Michael's Hospital","funders":"National Institute of Neurological Disorders and Stroke; Japan Society for the Promotion of Science; University of Texas MD Anderson Cancer Center; Servier; Fonds National de la Recherche Luxembourg; American Society of Clinical Oncology; Council for Higher Education; National Cancer Institute; National Institutes of Health; Conquer Cancer Foundation","keywords":"Biology; Glioblastoma; Ecosystem; Architecture; Computational biology; Evolutionary biology; Ecology; Genetics; Cancer research; Archaeology","score_opus":0.0046122928212065815,"score_gpt":0.23386749196159623,"score_spread":0.22925519914038964,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4410242531","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9876223,0.0007040834,0.009812494,0.00012694944,0.0000043570485,0.000009741217,0.0004625357,0.00009460587,0.0011630292],"genre_scores_gemma":[0.9951507,0.00028631743,0.003742216,0.00006436662,0.000005506999,0.000011715762,0.00035260562,0.00001902795,0.00036763606],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9997769,0.00003158196,0.0000140623915,0.00007716677,0.000054239837,0.00004604961],"domain_scores_gemma":[0.99981564,0.000034610082,0.00005725218,0.000031234995,0.000039637307,0.000021642123],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00020708564,0.00009953298,0.00021306664,0.00050191645,0.00022925454,0.0007422793,0.00014705086,0.00014631139,0.00026402253],"category_scores_gemma":[0.00030124554,0.00015975114,0.0001821058,0.00044139702,0.00049000024,0.0004978471,0.0004652215,0.00020269203,0.00010456991],"study_design_candidate":"bench_or_experimental","study_design_consensus":"bench_or_experimental","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00016574921,0.000013385037,0.064668976,0.000098845085,0.000048605463,0.00019770385,0.0005779117,0.0029736757,0.9079607,0.0032040395,0.00022084019,0.019869696],"study_design_scores_gemma":[0.000009929053,0.00021948051,0.7534931,0.000044548306,0.00009764668,0.001174886,0.0017169924,0.019810336,0.19824015,0.013975374,0.01113256,0.000085121435],"about_ca_topic_score_codex":0.0014954176,"about_ca_topic_score_gemma":0.0028723818,"teacher_disagreement_score":0.0014954176,"about_ca_system_score_codex":0.00040211072,"about_ca_system_score_gemma":0.0003029578,"threshold_uncertainty_score":0.0029734373},"labels":[],"label_agreement":null},{"id":"W4410325451","doi":"10.1038/s41588-025-02189-z","title":"Genome-wide analyses identify 30 loci associated with obsessive–compulsive disorder","year":2025,"lang":"en","type":"review","venue":"Nature Genetics","topic":"Obsessive-Compulsive Spectrum Disorders","field":"Psychology","cited_by":48,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Calgary; BC Mental Health & Substance Use Services; Health Sciences Centre; Sunnybrook Health Science Centre; McMaster University; BC Children's Hospital; Dalhousie University; University of Toronto; Centre for Addiction and Mental Health; University of British Columbia; Hospital for Sick Children","funders":"FP7 Health; Jane and Terry Semel Institute for Neuroscience and Human Behavior, University of California, Los Angeles; Eunice Kennedy Shriver National Institute of Child Health and Human Development; NIH Clinical Center; National Center for Research Resources; National Institute of Neurological Disorders and Stroke; National Institute on Drug Abuse; National Institute of Mental Health; National Heart, Lung, and Blood Institute; National Institute on Aging; National Institute on Alcohol Abuse and Alcoholism; Norwegian Institute of Public Health; Faculty of Medicine and Health, University of Sydney; National Institute of General Medical Sciences; Center for Innovative Medicine; Neuroscience Center Zurich, University of Zurich; Agència de Gestió d'Ajuts Universitaris i de Recerca; National Health and Medical Research Council; National Human Genome Research Institute; Department of Psychiatry, Columbia University; Yale University; Feinberg School of Medicine; Instituto Nacional de Medicina Genómica; National Institutes of Health; Ingham Institute for Applied Medical Research; Cumming School of Medicine, University of Calgary; Gentofte Hospital; King's College London; St. Olavs Hospital Universitetssykehuset i Trondheim; Deutsche Forschungsgemeinschaft; Ontario Council on Graduate Studies, Council of Ontario Universities; Assistance publique-Hôpitaux de Paris; Department of Health and Social Care; Novo Nordisk Fonden; Universität zu Köln; Universitat de Barcelona; Forskningsrådet om Hälsa, Arbetsliv och Välfärd; H. Lundbeck A/S; Institut National de la Santé et de la Recherche Médicale; Humboldt-Universität zu Berlin; U.S. Department of Veterans Affairs; Region Hovedstaden; Universitetet i Bergen; Helse Midt-Norge; Vetenskapsrådet; Novo Nordisk; Universitetet i Oslo; Lundbeckfonden; Université Paris-Est Créteil Val-de-Marne; Universiteit Stellenbosch; AFA Försäkring; Koninklijke Nederlandse Akademie van Wetenschappen; Institute of Psychiatry, Psychology and Neuroscience, King’s College London; Brown University; National Center for Advancing Translational Sciences; Bundesministerium für Bildung und Forschung; Karolinska Institutet; Department of Psychiatry, Faculty of Medicine, University of British Columbia; National Institute for Health and Care Research; University of Queensland; NIHR Maudsley Biomedical Research Centre; Rijksuniversiteit Groningen; Ministero della Salute; Centro de Investigación Biomédica en Red de Salud Mental; National Research Foundation; South African Medical Research Council; Deutsches Zentrum für Neurodegenerative Erkrankungen; National Center for PTSD, U.S. Department of Veterans Affairs; Queensland Health; Mathison Centre for Mental Health Research and Education; Stichting Volksbond Rotterdam; Della Martin Foundation; QIMR Berghofer Medical Research Institute; Vanderbilt University Medical Center; European College of Neuropsychopharmacology; Vrije Universiteit Amsterdam; Amsterdam Neuroscience; Aarhus Universitetshospital; Beatrice and Samuel A. Seaver Foundation; Aarhus Universitet; Stockholms Läns Landsting; Norges Forskningsråd; Ministero dell’Istruzione, dell’Università e della Ricerca; Fakultet for medisin og helsevitenskap, Norges Teknisk-Naturvitenskapelige Universitet; Instituto de Salud Carlos III; Università degli Studi di Milano; Fudan University; Göteborgs Universitet; Trond Mohn stiftelse; Hospital for Sick Children; Massachusetts General Hospital; Klarman Family Foundation; Ministerio de Ciencia, Innovación y Universidades; BC Children's Hospital; Helse- og Omsorgsdepartementet; South London and Maudsley NHS Foundation Trust; Office of Research and Development; Universitair Medisch Centrum Groningen; European Regional Development Fund; International OCD Foundation; Universitat Autònoma de Barcelona; Eidgenössische Technische Hochschule Zürich; European Social Fund; Medical Research Council; Tartu Ülikool; Fundació la Marató de TV3; Johns Hopkins University; Northwestern University; European Commission; Helsingin Yliopisto; Universität Zürich; University of Cape Town; Georgia Clinical and Translational Science Alliance; School of Medicine, Indiana University; University of New South Wales; University of North Carolina at Chapel Hill; Wayne State University; Universitätsspital Zürich; Vanderbilt University","keywords":"Genome-wide association study; Biology; Genetics; Genetic architecture; Heritability; Genetic association; Single-nucleotide polymorphism; Gene; Phenotype; Genotype","score_opus":0.02637258384594438,"score_gpt":0.38352011073510034,"score_spread":0.35714752688915596,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4410325451","genre_codex":"review","genre_gemma":"review","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"review","genre_consensus":"review","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.00046141032,0.9988907,0.00006296728,0.00015147188,0.00004088857,0.0000033881413,0.000056481247,0.0000057256434,0.00032702173],"genre_scores_gemma":[0.0037013397,0.9956149,0.00015624354,0.00015989337,0.000048865884,0.0000066182374,0.00012091321,0.0000016131534,0.00018954591],"study_design_codex":"design_other","study_design_gemma":"observational","domain_scores_codex":[0.99982363,0.000037466394,0.00003334288,0.000040714087,0.00004938791,0.00001548949],"domain_scores_gemma":[0.99967456,0.00018081129,0.00005884802,0.000007657766,0.00005504492,0.000023057528],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00061554374,0.0007498304,0.0016542776,0.0019263863,0.00012044469,0.000599407,0.000742585,0.0006314423,0.0024891258],"category_scores_gemma":[0.0006966312,0.00022220671,0.0008830648,0.0022290216,0.00025940101,0.00031377736,0.0004651736,0.00058238965,0.0006016091],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0003140658,0.000043029166,0.002973107,0.03648681,0.0018508001,0.0003783053,0.000053274376,0.00027897916,0.001199899,0.00081256154,0.014001804,0.9416074],"study_design_scores_gemma":[0.00050360843,0.0005398493,0.06278523,0.033083268,0.013024484,0.007984443,0.00030054376,0.00043327734,0.0017337358,0.003320426,0.8761668,0.00012430579],"about_ca_topic_score_codex":0.0018377415,"about_ca_topic_score_gemma":0.0030409894,"teacher_disagreement_score":0.0024891258,"about_ca_system_score_codex":0.00036521308,"about_ca_system_score_gemma":0.00084712205,"threshold_uncertainty_score":0.008326948},"labels":[],"label_agreement":null},{"id":"W4410447561","doi":"10.1038/s41588-025-02184-4","title":"Dominant variants in major spliceosome U4 and U5 small nuclear RNA genes cause neurodevelopmental disorders through splicing disruption","year":2025,"lang":"en","type":"article","venue":"Nature Genetics","topic":"RNA Research and Splicing","field":"Biochemistry, Genetics and Molecular Biology","cited_by":42,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"McMaster University; McMaster Children's Hospital; Alberta Children's Hospital; University of Calgary; Children's Hospital of Eastern Ontario; University of Ottawa; Hospital for Sick Children","funders":"National Human Genome Research Institute; Canadian Institutes of Health Research; Genome Alberta; Alberta Innovates; Austrian Science Fund; ZonMw; Institut National de la Santé et de la Recherche Médicale; European Commission; Medical Research Council; Department of Health and Social Care; Generalitat de Catalunya; National Institute for Health and Care Research; Wellcome Trust; Cancer Research UK; Alberta Children's Hospital Foundation; Genome British Columbia; Centres de Recerca de Catalunya; Ontario Genomics Institute; Australian Government; State Government of Victoria; Cold Spring Harbor Laboratory; Deutsche Forschungsgemeinschaft; Children's Hospital Foundation; Région Normandie; Murdoch Children's Research Institute; New York Genome Center; Genome Canada; Ontario Genomics; Royal Society; Fundación Hesperia; Children’s Hospital of Wisconsin Research Institute","keywords":"Biology; Spliceosome; RNA splicing; Genetics; Gene; Small nuclear RNA; Intron; RNA; Computational biology; Non-coding RNA","score_opus":0.007778530674980407,"score_gpt":0.27078246068957595,"score_spread":0.26300393001459554,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4410447561","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99598986,0.0012240979,0.0015684569,0.000051017185,0.0000070140436,0.000008259497,0.00023649914,0.00003288299,0.00088198273],"genre_scores_gemma":[0.9981993,0.00038985533,0.0006616729,0.000026972704,0.00000908345,0.0000032592477,0.00018507129,0.0000069029143,0.00051798555],"study_design_codex":"observational","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9996228,0.00007550637,0.000035793273,0.00013895112,0.00007508493,0.000051888775],"domain_scores_gemma":[0.9996642,0.00008567639,0.00015143772,0.000027832564,0.000026217986,0.00004463625],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0002995955,0.0006814396,0.00029421735,0.0010532406,0.00038072164,0.00032302324,0.0003154706,0.00032774455,0.002098754],"category_scores_gemma":[0.0007766485,0.00012115437,0.00029267246,0.00064761704,0.00040048355,0.00017489953,0.00035025054,0.00017442921,0.00031109003],"study_design_candidate":"bench_or_experimental","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00070109137,0.00009007219,0.77330667,0.00012219761,0.0004320337,0.016250154,0.0008315208,0.0006666634,0.16311365,0.0020493018,0.00072146597,0.041715227],"study_design_scores_gemma":[0.000044456327,0.0004058972,0.8945816,0.000057319096,0.00035988048,0.041646224,0.00065268716,0.0016192128,0.05254766,0.0010406468,0.0070092636,0.000035085275],"about_ca_topic_score_codex":0.0059816656,"about_ca_topic_score_gemma":0.006875389,"teacher_disagreement_score":0.0059816656,"about_ca_system_score_codex":0.0003819908,"about_ca_system_score_gemma":0.00029604064,"threshold_uncertainty_score":0.01189369},"labels":[],"label_agreement":null},{"id":"W4410552483","doi":"10.1038/s41588-025-02100-w","title":"Genome-wide association study of long COVID","year":2025,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Long-Term Effects of COVID-19","field":"Medicine","cited_by":36,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Simon Fraser University; McGill University Health Centre; Institut universitaire de cardiologie et de pneumologie de Québec; McGill Genome Centre; Lunenfeld-Tanenbaum Research Institute; Mount Sinai Hospital; Centre Hospitalier de l’Université de Montréal; McGill University; University of Toronto; Jewish General Hospital","funders":"National Institute of Allergy and Infectious Diseases; National Institute on Aging; Instituto de Investigaciones Biomédicas, Universidad Nacional Autónoma de México; Medizinische Fakultät, Rheinische Friedrich-Wilhelms-Universität Bonn; School of Public Health, Imperial College London; RIKEN; Department of Epidemiology, Biostatistics and Occupational Health, McGill University; Knight Cancer Institute, Oregon Health and Science University; Stanley Center for Psychiatric Research, Broad Institute; University of California, San Francisco; Tehran University of Medical Sciences and Health Services; National Institutes of Health; University of Ioannina; Universitair Medisch Centrum Groningen; Rheinische Friedrich-Wilhelms-Universität Bonn; Universidad de Chile; Rijksuniversiteit Groningen; Universidad Nacional Autónoma de México; Technische Universität München; Universität Regensburg; Imperial College London; University of Toronto; Universiti Malaysia Pahang; Universidad de Talca; Universitätsklinikum Regensburg; Sjællands Universitetshospital; Japan Society for the Promotion of Science; Universitetet i Bergen; Jewish General Hospital; University of Bristol; University Hospitals of Leicester NHS Trust; International Islamic University Malaysia; Max-Planck-Gesellschaft; King's College London; Faculty of Health and Medical Sciences, University of Western Australia; University of Leicester; Norwegian Institute of Public Health; Helsingin ja Uudenmaan Sairaanhoitopiiri; University of Washington; Università degli Studi di Milano; University of Pennsylvania Health System; Barts and The London School of Medicine and Dentistry; University of Essex; Wellcome Trust; Novo Nordisk; NIHR Leicester Biomedical Research Centre; University of Pennsylvania; Keio University; National Institute for Health and Care Research; Helsinki Institute of Life Science, Helsingin Yliopisto; Aarhus Universitetshospital; Det Sundhedsvidenskabelige Fakultet, Københavns Universitet; Queen Mary University of London; National Center for Advancing Translational Sciences; Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico; Understanding Society; Helsingin Yliopisto; McGill University; Brigham and Women's Hospital; Argonne National Laboratory; Medical Research Council; Tartu Ülikool; Università degli Studi di Siena; Massachusetts General Hospital; Broad Institute; Aarhus Universitet","keywords":"Biology; Genome-wide association study; Shingles; Coronavirus disease 2019 (COVID-19); Population; Disease; Immunology; Coronavirus; Rhinovirus; Medicine; Single-nucleotide polymorphism; Genetics; Virus; Infectious disease (medical specialty); Pathology; Genotype; Gene","score_opus":0.006827765649132134,"score_gpt":0.3078010744980689,"score_spread":0.3009733088489368,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4410552483","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9952956,0.001526319,0.0006984497,0.00020718412,0.000043791137,0.000010746873,0.0012804886,0.000016255903,0.0009211727],"genre_scores_gemma":[0.9982405,0.00024331833,0.00036283187,0.00008012722,0.00002236161,0.000011400952,0.00068793003,0.000008417301,0.00034310046],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9986091,0.0004623324,0.00011859046,0.0005240759,0.00012915715,0.00015676858],"domain_scores_gemma":[0.99844766,0.0005497734,0.00040347467,0.0002166494,0.00015969668,0.0002226751],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0014799915,0.00032458032,0.0003987329,0.0008107743,0.000688868,0.0006212492,0.00039477373,0.00067587703,0.0027858315],"category_scores_gemma":[0.0023920292,0.00021107719,0.000935618,0.0014115685,0.0003101465,0.00026154367,0.00062040513,0.0007674532,0.00019697624],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0010337917,0.00005339537,0.9852077,0.00007525417,0.0019840216,0.00078310637,0.00013114588,0.00015262976,0.0050460547,0.000267472,0.000749252,0.004516127],"study_design_scores_gemma":[0.000056866484,0.00018121922,0.99600804,0.000019560777,0.0006767004,0.000664711,0.00011141245,0.00034141794,0.00039347817,0.00016627231,0.001370977,0.000009399238],"about_ca_topic_score_codex":0.0061343554,"about_ca_topic_score_gemma":0.0093168225,"teacher_disagreement_score":0.0061343554,"about_ca_system_score_codex":0.00029110545,"about_ca_system_score_gemma":0.0003244872,"threshold_uncertainty_score":0.012197316},"labels":[],"label_agreement":null},{"id":"W4410754678","doi":"10.1038/s41588-025-02172-8","title":"Base editing of trinucleotide repeats that cause Huntington’s disease and Friedreich’s ataxia reduces somatic repeat expansions in patient cells and in mice","year":2025,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Genetic Neurodegenerative Diseases","field":"Neuroscience","cited_by":24,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Université Laval","funders":"National Institute of Biomedical Imaging and Bioengineering; National Institute of Allergy and Infectious Diseases; National Institute of General Medical Sciences; National Institute of Neurological Disorders and Stroke; National Human Genome Research Institute; National Heart, Lung, and Blood Institute","keywords":"Trinucleotide repeat expansion; Ataxia; Biology; Genetics; Allele; Somatic cell; Huntington's disease; Gene; Disease; Neuroscience; Pathology; Medicine","score_opus":0.015463030358325268,"score_gpt":0.263066599348996,"score_spread":0.24760356899067074,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4410754678","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9909679,0.00079352345,0.005408623,0.00008400639,0.00004214646,0.000056339493,0.00020850198,0.00017213878,0.0022667907],"genre_scores_gemma":[0.98905355,0.000567488,0.006579239,0.00007091254,0.000011549996,0.00003570865,0.00041897708,0.00005511593,0.003207482],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9998456,0.000028888517,0.000019642888,0.000037390935,0.00004801366,0.000020337302],"domain_scores_gemma":[0.9999056,0.000021151276,0.000030134504,0.000011282209,0.000008020291,0.000023796722],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00019685965,0.00030832688,0.00022698341,0.00020660619,0.00010401071,0.00020737016,0.00021809728,0.00036975383,0.0011980365],"category_scores_gemma":[0.00014875334,0.00010993924,0.00016408482,0.00007190187,0.00017835172,0.0001009001,0.00016448727,0.00038968874,0.00022593081],"study_design_candidate":"bench_or_experimental","study_design_consensus":"bench_or_experimental","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00003671872,0.000031210093,0.00007648483,0.0000115284565,0.000007620397,0.000045297613,0.000013475689,0.000054626165,0.99828416,0.00009401866,0.00003139009,0.0013134046],"study_design_scores_gemma":[0.00003199237,0.0006278736,0.0022517594,0.000008757796,0.000030060586,0.00070659874,0.00001574204,0.0008787166,0.9919859,0.00008180633,0.0033750068,0.000005786518],"about_ca_topic_score_codex":0.0004322275,"about_ca_topic_score_gemma":0.0009947015,"teacher_disagreement_score":0.0011980365,"about_ca_system_score_codex":0.00012734746,"about_ca_system_score_gemma":0.00013414945,"threshold_uncertainty_score":0.0040078163},"labels":[],"label_agreement":null},{"id":"W4411152766","doi":"10.1038/s41588-025-02251-w","title":"Author Correction: Comprehensive molecular profiling of multiple myeloma identifies refined copy number and expression subtypes","year":2025,"lang":"en","type":"erratum","venue":"Nature Genetics","topic":"Multiple Myeloma Research and Treatments","field":"Medicine","cited_by":0,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"McGill University; Alberta Cancer Foundation; Royal Victoria Hospital; Princess Margaret Cancer Centre","funders":"","keywords":"Biology; Gene expression profiling; Multiple myeloma; Profiling (computer programming); Computational biology; Expression (computer science); Genetics; Gene expression; Gene; Immunology; Computer science","score_opus":0.017310649407687406,"score_gpt":0.33100820473314657,"score_spread":0.3136975553254592,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4411152766","genre_codex":"editorial","genre_gemma":"other","domain_codex":null,"domain_gemma":"reproducibility","model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"other","genre_consensus":null,"domain_candidate":"reproducibility","domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.000456193,0.0011862909,0.0024541307,0.053091113,0.93721044,0.000024286152,0.0014447992,0.00063629093,0.0034963526],"genre_scores_gemma":[0.040715326,0.014070954,0.019125832,0.1273951,0.33469626,0.000246713,0.0073571177,0.004770819,0.45162192],"study_design_codex":"not_applicable","study_design_gemma":"not_applicable","domain_scores_codex":[0.99570835,0.0005775957,0.00067927985,0.0006984711,0.002014798,0.00032145958],"domain_scores_gemma":[0.9760182,0.0058891345,0.0012257604,0.0015774111,0.014328815,0.00096075714],"candidate_categories":["metaresearch"],"consensus_categories":[],"category_scores_codex":[0.004042529,0.0016506558,0.0014371093,0.0026958059,0.0028057392,0.0030918797,0.0029594712,0.0051371804,0.046420567],"category_scores_gemma":[0.046654243,0.0009295802,0.0012037904,0.001889437,0.0018655431,0.0017064315,0.0016573375,0.00963503,0.023842053],"study_design_candidate":"not_applicable","study_design_consensus":"not_applicable","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.000053154155,0.0000075402204,0.00013683357,0.00010446026,0.000016978072,0.0006472001,0.000049264636,0.000055819033,0.00020641515,0.0012266482,0.9888347,0.00866101],"study_design_scores_gemma":[0.000056012315,0.000024644301,0.0007945073,0.00031966716,0.00007451302,0.003065729,0.00009402885,0.00036263198,0.0012938158,0.0021926342,0.99166834,0.000053422405],"about_ca_topic_score_codex":0.012388019,"about_ca_topic_score_gemma":0.014891562,"teacher_disagreement_score":0.9959575,"about_ca_system_score_codex":0.0027981303,"about_ca_system_score_gemma":0.004632837,"threshold_uncertainty_score":0.15529227},"labels":[],"label_agreement":null},{"id":"W4411158027","doi":"10.1038/s41588-025-02203-4","title":"Coordinated function of paired NLRs confers Yr84-mediated stripe rust resistance in wheat","year":2025,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Wheat and Barley Genetics and Pathology","field":"Agricultural and Biological Sciences","cited_by":25,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Agriculture and Agri-Food Canada; University of Manitoba; University of Saskatchewan","funders":"","keywords":"Biology; Effector; Gene; Genetics; Phenotype; Cloning (programming); Positional cloning; Function (biology); Computational biology; Rust (programming language); Cell biology","score_opus":0.009638232628739755,"score_gpt":0.21907292969967035,"score_spread":0.2094346970709306,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4411158027","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9960318,0.00027439857,0.0024987883,0.000057211797,0.000024777351,0.000010717911,0.00012369809,0.00011994766,0.00085856207],"genre_scores_gemma":[0.99614644,0.000056523993,0.0015670175,0.00006471639,0.000008019339,0.000013171439,0.00027098728,0.000048523663,0.0018244586],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99970895,0.000048310358,0.0000353557,0.00009641559,0.000063182604,0.00004776688],"domain_scores_gemma":[0.99974793,0.000031644653,0.000075991404,0.000052226325,0.000025805357,0.000066334374],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0001809249,0.00026702773,0.00037694324,0.00021892691,0.00017884983,0.00040326698,0.00027048535,0.00039241457,0.0015896927],"category_scores_gemma":[0.00025912092,0.00025730138,0.0003437808,0.0001169189,0.00026935432,0.00031781165,0.0006333053,0.00074544875,0.00090088823],"study_design_candidate":"bench_or_experimental","study_design_consensus":"bench_or_experimental","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.000049564856,0.0000069385887,0.00011063091,0.000006178617,0.0000015823919,0.000035195382,0.0000054600773,0.000023239822,0.9993881,0.000032001386,0.000014103356,0.00032701984],"study_design_scores_gemma":[0.00007373915,0.00028910217,0.055565152,0.000007844235,0.000032544103,0.0010460153,0.00013346146,0.0041347616,0.93613446,0.00024290368,0.0023200046,0.000019927229],"about_ca_topic_score_codex":0.0002041607,"about_ca_topic_score_gemma":0.00039955787,"teacher_disagreement_score":0.0015896927,"about_ca_system_score_codex":0.0002812307,"about_ca_system_score_gemma":0.00013710758,"threshold_uncertainty_score":0.0053180456},"labels":[],"label_agreement":null},{"id":"W4411246386","doi":"10.1038/s41588-025-02218-x","title":"A scalable gut epithelial organoid model reveals the genome-wide colonization landscape of a human-adapted pathogen","year":2025,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Viral gastroenteritis research and epidemiology","field":"Medicine","cited_by":18,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"GreenField Specialty Alcolhols (Canada); University of Toronto","funders":"Stiftelsen för Strategisk Forskning; Science for Life Laboratory; Carl Tryggers Stiftelse för Vetenskaplig Forskning; Vetenskapsrådet; Stiftelsen för Strategisk Forskning; Kempestiftelserna; Stiftelsen Clas Groschinskys Minnesfond; European Society of Clinical Microbiology and Infectious Diseases","keywords":"Organoid; Biology; Colonization; Genome; Computational biology; Pathogen; Gene; Evolutionary biology; Genetics; Microbiology","score_opus":0.014764864508097384,"score_gpt":0.3056293774235365,"score_spread":0.29086451291543913,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4411246386","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.92218024,0.00048408995,0.07245133,0.00018488958,0.00003637391,0.000029010267,0.0023664262,0.00041839154,0.0018493129],"genre_scores_gemma":[0.97410357,0.00043510477,0.023051415,0.000033959022,0.0000033145216,0.000049138198,0.0012363596,0.000041306794,0.0010457777],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9999145,0.00001678685,0.000003391087,0.000032848693,0.000020119549,0.000012366319],"domain_scores_gemma":[0.99985194,0.00005117146,0.000032920772,0.000022615437,0.000014492304,0.000026846688],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00015872912,0.00032164194,0.00029387645,0.00022826451,0.00014920352,0.00036118474,0.0004150896,0.00043354803,0.00095456897],"category_scores_gemma":[0.00017725212,0.0002038314,0.0003135462,0.00023013582,0.00025441337,0.00017757523,0.00040327618,0.00057964877,0.00020674453],"study_design_candidate":"bench_or_experimental","study_design_consensus":"bench_or_experimental","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00021215732,0.00005421831,0.0019191261,0.00007642632,0.000022419468,0.0001671179,0.00004512913,0.06900798,0.9250807,0.0012603647,0.0001945254,0.0019598352],"study_design_scores_gemma":[0.00007301957,0.0009006113,0.013574223,0.000027080621,0.000085417785,0.00039891596,0.00033995585,0.56761944,0.4089627,0.0024086188,0.005541163,0.00006892367],"about_ca_topic_score_codex":0.0043403124,"about_ca_topic_score_gemma":0.0046018357,"teacher_disagreement_score":0.0043403124,"about_ca_system_score_codex":0.00040196546,"about_ca_system_score_gemma":0.00037147026,"threshold_uncertainty_score":0.008630097},"labels":[],"label_agreement":null},{"id":"W4411413853","doi":"10.1038/s41588-024-02046-5","title":"Publisher Correction: GWAS of multiple neuropathology endophenotypes identifies new risk loci and provides insights into the genetic risk of dementia","year":2025,"lang":"en","type":"erratum","venue":"Nature Genetics","topic":"Health, Environment, Cognitive Aging","field":"Environmental Science","cited_by":2,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Toronto","funders":"National Institute on Aging","keywords":"Neuropathology; Endophenotype; Genome-wide association study; Biology; Dementia; Genetic architecture; Genetics; Computational biology; Neuroscience; Bioinformatics; Single-nucleotide polymorphism; Disease; Quantitative trait locus; Internal medicine; Gene; Medicine; Cognition; Genotype","score_opus":0.005711984276603912,"score_gpt":0.22464317869553294,"score_spread":0.21893119441892903,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4411413853","genre_codex":"editorial","genre_gemma":"other","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"other","genre_consensus":null,"domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.00016720207,0.00047748277,0.0010780779,0.034827914,0.95772195,0.00002044154,0.001689983,0.0005184191,0.0034985947],"genre_scores_gemma":[0.019509414,0.0065476676,0.013521279,0.0898386,0.3464785,0.0002819852,0.008339165,0.0047581783,0.51072526],"study_design_codex":"not_applicable","study_design_gemma":"not_applicable","domain_scores_codex":[0.9944885,0.00076066056,0.0009891819,0.00073065376,0.0026612044,0.0003697272],"domain_scores_gemma":[0.95990807,0.008604383,0.0017069854,0.002789272,0.025617093,0.00137425],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.004756904,0.0023605195,0.0018193126,0.0038445597,0.0035650458,0.004507458,0.003672722,0.005392439,0.088500276],"category_scores_gemma":[0.06118304,0.0014333827,0.0016928769,0.0027996474,0.0018269522,0.0020725755,0.0017978033,0.012128668,0.03995926],"study_design_candidate":"not_applicable","study_design_consensus":"not_applicable","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00002743343,0.0000049289206,0.00008177552,0.00007163311,0.000011986322,0.00022636101,0.000025587064,0.000032635784,0.000059673715,0.00061673735,0.99473804,0.004103036],"study_design_scores_gemma":[0.000057634705,0.000018602837,0.00089844025,0.00035938807,0.00006817445,0.0010925495,0.000084401494,0.00032028032,0.00050317583,0.0019130977,0.99463415,0.000050098643],"about_ca_topic_score_codex":0.021461837,"about_ca_topic_score_gemma":0.033483066,"teacher_disagreement_score":0.088500276,"about_ca_system_score_codex":0.0030852377,"about_ca_system_score_gemma":0.005884616,"threshold_uncertainty_score":0.29606295},"labels":[],"label_agreement":null},{"id":"W4411414167","doi":"10.1038/s41588-024-02045-6","title":"Author Correction: GWAS of multiple neuropathology endophenotypes identifies new risk loci and provides insights into the genetic risk of dementia","year":2025,"lang":"en","type":"erratum","venue":"Nature Genetics","topic":"Health, Environment, Cognitive Aging","field":"Environmental Science","cited_by":0,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Toronto","funders":"National Institute on Aging","keywords":"Neuropathology; Endophenotype; Genome-wide association study; Biology; Dementia; Genetic architecture; Neuroscience; Genetics; Computational biology; Quantitative trait locus; Single-nucleotide polymorphism; Disease; Medicine; Cognition; Internal medicine; Gene; Genotype","score_opus":0.0070065176916676375,"score_gpt":0.24127214896830337,"score_spread":0.23426563127663574,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4411414167","genre_codex":"editorial","genre_gemma":"other","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"other","genre_consensus":null,"domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.00028456544,0.00046772408,0.004009006,0.037581418,0.9495206,0.00005147758,0.0033880596,0.0014126921,0.0032845011],"genre_scores_gemma":[0.03331331,0.0050669853,0.04978446,0.11087145,0.31140676,0.0007087496,0.016113691,0.012465663,0.46026886],"study_design_codex":"not_applicable","study_design_gemma":"not_applicable","domain_scores_codex":[0.99235314,0.0014020208,0.0015362367,0.0012679067,0.0030266182,0.0004140907],"domain_scores_gemma":[0.93178356,0.016601665,0.0031394756,0.005427562,0.041238893,0.0018088027],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0075532473,0.0022892156,0.0015754978,0.0033153521,0.002909004,0.003483335,0.003744435,0.0043236143,0.10591218],"category_scores_gemma":[0.10313649,0.0011959785,0.001907397,0.0023667768,0.0017708121,0.002099555,0.0023767767,0.0091329105,0.05477675],"study_design_candidate":"not_applicable","study_design_consensus":"not_applicable","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00003935184,0.000004997107,0.000113086535,0.00008855244,0.000014309846,0.00022557176,0.000034465047,0.000042644824,0.00008231969,0.00067616306,0.99326164,0.0054169344],"study_design_scores_gemma":[0.00006330798,0.000016453218,0.0007070741,0.0004135175,0.00006726239,0.0012461862,0.000089871246,0.00045351594,0.0007898279,0.002515761,0.99358386,0.000053302225],"about_ca_topic_score_codex":0.010531794,"about_ca_topic_score_gemma":0.016653284,"teacher_disagreement_score":0.10591218,"about_ca_system_score_codex":0.0028034719,"about_ca_system_score_gemma":0.0050867368,"threshold_uncertainty_score":0.35431153},"labels":[],"label_agreement":null},{"id":"W4411428667","doi":"10.1038/s41588-025-02227-w","title":"Transferability of European-derived Alzheimer’s disease polygenic risk scores across multiancestry populations","year":2025,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Genetic Associations and Epidemiology","field":"Biochemistry, Genetics and Molecular Biology","cited_by":17,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Ontario Brain Institute; Occupational Cancer Research Centre; University Health Network","funders":"National Institute of Neurological Disorders and Stroke; National Institute on Aging; National Heart, Lung, and Blood Institute; Fondation pour la Recherche sur Alzheimer; Fondation pour la Recherche Médicale; Institut National de la Santé et de la Recherche Médicale; U.S. Department of Veterans Affairs; EU Joint Programme – Neurodegenerative Disease Research; Université de Lille; Development of Innovative Strategies for a Transdisciplinary approach to ALZheimer's disease","keywords":"Biology; Polygenic risk score; Genome-wide association study; Apolipoprotein E; Genetic association; Disease; Genetics; Locus (genetics); Allele; Single-nucleotide polymorphism; Genotype; Gene; Internal medicine; Medicine","score_opus":0.021034349213429733,"score_gpt":0.330789409689605,"score_spread":0.3097550604761753,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4411428667","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9781829,0.00014010629,0.020351913,0.00008542144,0.000014906268,0.000037744612,0.00026980092,0.0000458514,0.0008712513],"genre_scores_gemma":[0.99700314,0.000051158346,0.0023877316,0.000027126418,0.0000065395743,0.000020523286,0.0003803624,0.000017261273,0.00010619115],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99000984,0.006784073,0.00042140685,0.0020329135,0.0004621368,0.00028957013],"domain_scores_gemma":[0.9723733,0.016307201,0.0024674044,0.0072263293,0.0010455296,0.00058026484],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.01648274,0.0007854118,0.0008110606,0.0019226574,0.0004953076,0.0011150711,0.0008271178,0.00056412845,0.0013898324],"category_scores_gemma":[0.042419545,0.000322741,0.0011302194,0.0013263728,0.00092360243,0.0010054073,0.0019976841,0.001075381,0.00019969714],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0016562119,0.0001842854,0.8991313,0.00008103753,0.004338969,0.00091966026,0.002461136,0.01401422,0.015037745,0.0043054307,0.0004305866,0.05743948],"study_design_scores_gemma":[0.00010499536,0.00037620767,0.9570858,0.000042908712,0.00047762314,0.0008794022,0.00030308487,0.03077478,0.0017088236,0.007465066,0.00072075013,0.000060660284],"about_ca_topic_score_codex":0.0038585311,"about_ca_topic_score_gemma":0.0020989967,"teacher_disagreement_score":0.01648274,"about_ca_system_score_codex":0.00042009618,"about_ca_system_score_gemma":0.00022378008,"threshold_uncertainty_score":0.087170124},"labels":[],"label_agreement":null},{"id":"W4412421032","doi":"10.1038/s41588-025-02250-x","title":"Germline genetic variation impacts clonal hematopoiesis landscape and progression to malignancy","year":2025,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Cancer Genomics and Diagnostics","field":"Biochemistry, Genetics and Molecular Biology","cited_by":16,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Queen's University","funders":"National Heart, Lung, and Blood Institute; National Institute on Aging; Science for Life Laboratory; Children's Discovery Institute; Edward P. Evans Foundation; Alexander and Margaret Stewart Trust; Swedish Cancer Foundation; National Cancer Institute; National Institutes of Health; Vetenskapsrådet; Prostate Cancer Foundation","keywords":"Biology; Germline; Haematopoiesis; Malignancy; Genetics; Genetic variation; Somatic evolution in cancer; Evolutionary biology; Variation (astronomy); Cancer; Gene; Stem cell","score_opus":0.002923274227631282,"score_gpt":0.26512362507667586,"score_spread":0.2622003508490446,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4412421032","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9978516,0.0005370824,0.00055410294,0.00004598895,0.0000038759663,0.0000035095607,0.00024041535,0.00001142378,0.00075208046],"genre_scores_gemma":[0.99930334,0.00015197512,0.00021735347,0.000020420252,0.0000034608763,0.0000014100672,0.00007692681,0.000004183844,0.0002209307],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99973637,0.0000556212,0.000013618529,0.00009205303,0.000066266264,0.000036095098],"domain_scores_gemma":[0.9996389,0.0001145036,0.00014687418,0.000027791968,0.000025811352,0.00004597353],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0002281616,0.00014544328,0.00015992214,0.00044040216,0.00021369859,0.00040290118,0.00012767369,0.0002260157,0.0020178305],"category_scores_gemma":[0.00096072856,0.00008450604,0.00017445433,0.00047850132,0.00025117194,0.00015118545,0.00023838074,0.0002791492,0.000119831675],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00033830982,0.000036012192,0.91053313,0.00004478491,0.00021946114,0.0009126712,0.00023390632,0.0008847245,0.054796685,0.00094501337,0.00037967126,0.030675692],"study_design_scores_gemma":[0.0000052455907,0.00009012244,0.9923063,0.000010720023,0.000053675,0.0014450552,0.00009838105,0.00068580284,0.0037119647,0.0005162379,0.0010692618,0.0000072441767],"about_ca_topic_score_codex":0.0020969422,"about_ca_topic_score_gemma":0.0034544591,"teacher_disagreement_score":0.0020969422,"about_ca_system_score_codex":0.00022094064,"about_ca_system_score_gemma":0.00015567805,"threshold_uncertainty_score":0.0067502856},"labels":[],"label_agreement":null},{"id":"W4412491996","doi":"10.1038/s41588-025-02255-6","title":"Therapeutic strategies for fragile X syndrome and implications for other gene-silencing disorders","year":2025,"lang":"en","type":"review","venue":"Nature Genetics","topic":"Genetics and Neurodevelopmental Disorders","field":"Biochemistry, Genetics and Molecular Biology","cited_by":3,"is_retracted":false,"has_abstract":false,"route_ca_aff":false,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"","funders":"Azrieli Foundation; Israel Science Foundation; Rosetrees Trust","keywords":"Fragile X syndrome; Gene silencing; Biology; Epigenetics; FMR1; Genetics; DNA methylation; Autism; Angelman syndrome; Trinucleotide repeat expansion; Gene; Chromosomal fragile site; Bioinformatics; Gene expression; Fragile x; Allele; Psychiatry; Medicine","score_opus":0.017630252073881213,"score_gpt":0.31977640095462107,"score_spread":0.3021461488807399,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4412491996","genre_codex":"review","genre_gemma":"review","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"review","genre_consensus":"review","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.00008365439,0.9980976,0.00027869962,0.0003552544,0.0002640092,0.0000052822315,0.000018340697,0.0000110704,0.0008860853],"genre_scores_gemma":[0.0007746307,0.99710983,0.0004592946,0.00046170384,0.0002402041,0.000015778942,0.000049947117,0.0000034879063,0.0008850865],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.99981016,0.00004112379,0.000021964544,0.000033467088,0.0000621935,0.000031082625],"domain_scores_gemma":[0.9997141,0.00017715002,0.00002780347,0.000008686439,0.00004438226,0.000027999818],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0010424391,0.0013311881,0.0018220979,0.0019366689,0.00028416226,0.0011218534,0.0015272871,0.0018579193,0.0044568516],"category_scores_gemma":[0.00096845935,0.00027659768,0.0007153494,0.0013439512,0.0008268519,0.001247732,0.00081350957,0.0031464216,0.0018301866],"study_design_candidate":"not_applicable","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00016652979,0.00013087537,0.000110796995,0.007860904,0.00012842311,0.00054501666,0.000039526007,0.0009062157,0.0018833718,0.009386702,0.047632888,0.9312088],"study_design_scores_gemma":[0.00009523528,0.00014753733,0.000538441,0.003020543,0.0001580799,0.0020672476,0.000045924706,0.00021430227,0.0005597841,0.0055732387,0.9875516,0.00002804153],"about_ca_topic_score_codex":0.0010304713,"about_ca_topic_score_gemma":0.0025645385,"teacher_disagreement_score":0.0044568516,"about_ca_system_score_codex":0.00090139953,"about_ca_system_score_gemma":0.0007155955,"threshold_uncertainty_score":0.014909625},"labels":[],"label_agreement":null},{"id":"W4412552430","doi":"10.1038/s41588-025-02259-2","title":"Genomics-driven discovery of superior alleles and genes for yellow rust resistance in wheat","year":2025,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Wheat and Barley Genetics and Pathology","field":"Agricultural and Biological Sciences","cited_by":21,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Institute of Genetics","funders":"","keywords":"Biology; Allele; Genomics; Genetics; Gene; Rust (programming language); Plant disease resistance; Computational biology; Biotechnology; Genome","score_opus":0.00922913166188219,"score_gpt":0.2292762491882895,"score_spread":0.22004711752640732,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4412552430","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9890589,0.00037333506,0.006992616,0.00031051922,0.00004338223,0.00007924296,0.0010612361,0.00009744159,0.0019833273],"genre_scores_gemma":[0.986187,0.0005440448,0.008577575,0.00028860496,0.00002052609,0.000028693923,0.0020156407,0.000078746634,0.0022591215],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99984884,0.00001936056,0.000012275212,0.000040535924,0.0000484672,0.00003043329],"domain_scores_gemma":[0.99986136,0.000049036647,0.000029635601,0.0000124183225,0.00001583589,0.000031682004],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0005469369,0.00023992191,0.00034666798,0.00034075894,0.00018291065,0.0006141426,0.00025319163,0.00038252596,0.00079898495],"category_scores_gemma":[0.00030855596,0.00019103361,0.000390667,0.0002751256,0.0003077683,0.00021831783,0.00053318235,0.0010605848,0.00021647387],"study_design_candidate":"bench_or_experimental","study_design_consensus":"bench_or_experimental","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00008111661,0.000029713514,0.0004828792,0.00002247572,0.000007258376,0.000069546804,0.00004285104,0.00022608589,0.9955037,0.0004402806,0.00006339723,0.0030306468],"study_design_scores_gemma":[0.00039868287,0.0013720267,0.090217344,0.000037640366,0.00023554728,0.0013378551,0.00055262813,0.011210743,0.87402385,0.0026511354,0.017896088,0.000066480294],"about_ca_topic_score_codex":0.0009073992,"about_ca_topic_score_gemma":0.0021942547,"teacher_disagreement_score":0.0009073992,"about_ca_system_score_codex":0.00037315316,"about_ca_system_score_gemma":0.0003360363,"threshold_uncertainty_score":0.0028924942},"labels":[],"label_agreement":null},{"id":"W4412692199","doi":"10.1038/s41588-025-02270-7","title":"The LISTEN principles for genetic sequence data governance and database engineering","year":2025,"lang":"en","type":"review","venue":"Nature Genetics","topic":"Research Data Management Practices","field":"Computer Science","cited_by":2,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Université de Montréal","funders":"National Science Foundation","keywords":"Biology; Sequence (biology); Corporate governance; Database; Genetics; Computational biology; Computer science; Business","score_opus":0.17710215780679933,"score_gpt":0.4198912806484852,"score_spread":0.24278912284168586,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4412692199","genre_codex":"review","genre_gemma":"review","domain_codex":null,"domain_gemma":"reproducibility","model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"review","genre_consensus":"review","domain_candidate":"reproducibility","domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.00009276101,0.97185475,0.0059243273,0.014720541,0.0010905223,0.000025674191,0.000051985353,0.000040327974,0.00619903],"genre_scores_gemma":[0.0020036055,0.97933793,0.0069571296,0.00808102,0.0011405759,0.00009170646,0.000090491136,0.000032051114,0.002265465],"study_design_codex":"design_other","study_design_gemma":"theoretical_or_conceptual","domain_scores_codex":[0.9936939,0.002451317,0.00071999273,0.0005017037,0.0023499462,0.00028312125],"domain_scores_gemma":[0.98133415,0.014064396,0.00097449654,0.00090114336,0.0023205676,0.00040525146],"candidate_categories":["metaresearch","open_science"],"consensus_categories":[],"category_scores_codex":[0.013712101,0.0010109517,0.0016987976,0.00578106,0.0010345328,0.0053192773,0.0024785013,0.0046464987,0.004602775],"category_scores_gemma":[0.021738378,0.0006688926,0.00096602226,0.007126059,0.007984682,0.007992947,0.0034082897,0.0070651807,0.002840826],"study_design_candidate":"theoretical_or_conceptual","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.000045381796,0.000060496914,0.00014537916,0.008512351,0.00010294268,0.0001284677,0.00025788997,0.0006034825,0.00036746342,0.24029855,0.08125637,0.6682212],"study_design_scores_gemma":[0.000015075361,0.000019098798,0.00014668808,0.006540107,0.00003611673,0.00015316978,0.00006796965,0.000104600345,0.0001790193,0.041350875,0.9513696,0.0000178281],"about_ca_topic_score_codex":0.005090232,"about_ca_topic_score_gemma":0.006028571,"teacher_disagreement_score":0.9975215,"about_ca_system_score_codex":0.0047917753,"about_ca_system_score_gemma":0.009497113,"threshold_uncertainty_score":0.072517335},"labels":[],"label_agreement":null},{"id":"W4412786071","doi":"10.1038/s41588-025-02272-5","title":"Why genomic diversity should not be framed by census alone","year":2025,"lang":"en","type":"letter","venue":"Nature Genetics","topic":"Race, Genetics, and Society","field":"Biochemistry, Genetics and Molecular Biology","cited_by":1,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Genome Canada","funders":"","keywords":"Biology; Diversity (politics); Census; Computational biology; Genetics; Evolutionary biology; Demography; Anthropology; Sociology; Population","score_opus":0.012121534420301524,"score_gpt":0.24863333132779872,"score_spread":0.23651179690749718,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4412786071","genre_codex":"commentary","genre_gemma":"commentary","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"commentary","genre_consensus":"commentary","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.00034115254,0.0005741378,0.0003574622,0.98467976,0.011473052,0.0000069144853,0.000023788036,0.000024748339,0.002519],"genre_scores_gemma":[0.0039646095,0.0002628461,0.00041502848,0.9763474,0.013899552,0.000027123097,0.000013538203,0.000024822704,0.0050451793],"study_design_codex":"not_applicable","study_design_gemma":"not_applicable","domain_scores_codex":[0.9888861,0.002966167,0.0008237467,0.0018448755,0.003759223,0.0017198812],"domain_scores_gemma":[0.95798826,0.024924755,0.0016257175,0.0021717893,0.006620865,0.006668569],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.017348152,0.00077684765,0.002058777,0.00094483193,0.0062773842,0.0057929535,0.0021213333,0.06432769,0.0075565297],"category_scores_gemma":[0.06397894,0.0009637663,0.001212254,0.0007666909,0.013961374,0.010733229,0.0035476023,0.07332489,0.006522475],"study_design_candidate":"not_applicable","study_design_consensus":"not_applicable","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00011228928,0.00005513455,0.0009433283,0.000051778414,0.000028901542,0.00048478702,0.00042069927,0.000091439535,0.00025136702,0.041335896,0.94248813,0.013736313],"study_design_scores_gemma":[0.0001822509,0.000069708934,0.0019634247,0.00026284778,0.00003481631,0.0004846747,0.0011077166,0.0005316867,0.00037437884,0.12974167,0.86511123,0.00013567135],"about_ca_topic_score_codex":0.01666289,"about_ca_topic_score_gemma":0.022104759,"teacher_disagreement_score":0.06432769,"about_ca_system_score_codex":0.006085362,"about_ca_system_score_gemma":0.006874402,"threshold_uncertainty_score":0.09174693},"labels":[],"label_agreement":null},{"id":"W4412929242","doi":"10.1038/s41588-025-02269-0","title":"Uncovering the multivariate genetic architecture of frailty with genomic structural equation modeling","year":2025,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Frailty in Older Adults","field":"Medicine","cited_by":14,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Nova Scotia Health Authority; Dalhousie University","funders":"National Institute of Mental Health; National Institute on Aging; Economic and Social Research Council; Medical Research Council; National Health and Medical Research Council; Dalhousie University; Natural Sciences and Engineering Research Council of Canada; Alzheimer’s Research UK; National Institute for Health and Care Research; University of Edinburgh; University of Exeter; Multiple Sclerosis Society; Age UK; Government of the United Kingdom; Directorate for Biological Sciences; U.S. Department of Health and Human Services; Government of Canada; Wellcome Trust; Canadian Institutes of Health Research; Wellcome","keywords":"Biology; Multivariate statistics; Structural equation modeling; Genetic architecture; Multivariate analysis; Computational biology; Evolutionary biology; Genetics; Statistics; Phenotype; Gene; Mathematics","score_opus":0.015640617736420625,"score_gpt":0.2824250891734066,"score_spread":0.26678447143698597,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4412929242","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.7666731,0.0018807806,0.22461453,0.0035436454,0.00010606868,0.00007457144,0.0018162904,0.00037283055,0.0009181332],"genre_scores_gemma":[0.9705702,0.00050913147,0.027416062,0.00021797958,0.00007810301,0.00005717087,0.00071067363,0.00003682084,0.0004037581],"study_design_codex":"observational","study_design_gemma":"simulation_or_modeling","domain_scores_codex":[0.9974152,0.0017304794,0.00007800406,0.0004853339,0.00011975351,0.00017126158],"domain_scores_gemma":[0.9889304,0.008823381,0.0007661223,0.0009973365,0.00024067574,0.00024195532],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0062900484,0.0013264826,0.0013997988,0.0022528288,0.0006974177,0.0014367733,0.001154125,0.0010809257,0.00207918],"category_scores_gemma":[0.02003385,0.000850716,0.0025668703,0.0026664485,0.0008971466,0.0012095061,0.0018385559,0.0024875102,0.00022589313],"study_design_candidate":"simulation_or_modeling","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0004578634,0.00042594367,0.76634026,0.00017750845,0.006849013,0.0007007752,0.00092175626,0.10842617,0.0019578037,0.03280819,0.003342923,0.07759175],"study_design_scores_gemma":[0.00015133589,0.00018991354,0.1742933,0.00013104602,0.002108908,0.00031218393,0.0004825723,0.6343019,0.00035573455,0.18574473,0.0018401918,0.00008823246],"about_ca_topic_score_codex":0.024973875,"about_ca_topic_score_gemma":0.02858724,"teacher_disagreement_score":0.024973875,"about_ca_system_score_codex":0.0006568209,"about_ca_system_score_gemma":0.0017100996,"threshold_uncertainty_score":0.049656987},"labels":[],"label_agreement":null},{"id":"W4412954320","doi":"10.1038/s41588-025-02249-4","title":"Single-nucleus chromatin accessibility profiling identifies cell types and functional variants contributing to major depression","year":2025,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Nuclear Receptors and Signaling","field":"Neuroscience","cited_by":18,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"McGill University; Douglas Mental Health University Institute","funders":"Fonds de recherche du Québec – Nature et technologies; Canadian Institutes of Health Research; Canadian Network for Research and Innovation in Machining Technology, Natural Sciences and Engineering Research Council of Canada; Government of Canada; Fonds de Recherche du Québec - Santé; Foundation for the National Institutes of Health","keywords":"Biology; Chromatin; Profiling (computer programming); Computational biology; Nucleus; Genetics; Evolutionary biology; Neuroscience; Gene","score_opus":0.01565939827284158,"score_gpt":0.2723307282673508,"score_spread":0.2566713299945092,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4412954320","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9969875,0.00028030138,0.0016493334,0.00005533111,0.000010222857,0.0000059396925,0.00051723066,0.000022151966,0.00047202714],"genre_scores_gemma":[0.9986527,0.00014061731,0.00044908942,0.000029050749,0.0000036384517,0.000005699516,0.00026196442,0.000014819541,0.00044226064],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.99985576,0.000013583213,0.000010232341,0.00006081991,0.000027753233,0.00003185157],"domain_scores_gemma":[0.9998288,0.000043226508,0.000053665077,0.000023524359,0.000020053329,0.000030727875],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0001277208,0.0001643004,0.0002222419,0.0004203085,0.00013731548,0.00035668266,0.00022874385,0.0002336793,0.0021744736],"category_scores_gemma":[0.00031307782,0.00018299682,0.00024426752,0.00025974054,0.00021597414,0.00011665975,0.00023664294,0.00035638714,0.0002676609],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00030019126,0.000021374146,0.025559613,0.00002616763,0.000065955406,0.00019133267,0.00009287774,0.00008869152,0.96920544,0.00020672455,0.00014114367,0.004100548],"study_design_scores_gemma":[0.000034247867,0.00018207172,0.85961473,0.000015091417,0.00014492865,0.0021387036,0.00034670543,0.0017717713,0.13406092,0.0005236447,0.001148008,0.000019222856],"about_ca_topic_score_codex":0.002083752,"about_ca_topic_score_gemma":0.005908996,"teacher_disagreement_score":0.0021744736,"about_ca_system_score_codex":0.00021684427,"about_ca_system_score_gemma":0.00009905011,"threshold_uncertainty_score":0.0072743297},"labels":[],"label_agreement":null},{"id":"W4413874662","doi":"10.1038/s41588-025-02306-y","title":"Inactivation of β-1,3-glucan synthase-like 5 confers broad-spectrum resistance to Plasmodiophora brassicae pathotypes in cruciferous plants","year":2025,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Plant Disease Resistance and Genetics","field":"Agricultural and Biological Sciences","cited_by":13,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Saskatchewan","funders":"","keywords":"Biology; Cruciferous vegetables; Clubroot; Brassica; Broad spectrum; Microbiology; Botany; Genetics","score_opus":0.007080188952593669,"score_gpt":0.23037621671575362,"score_spread":0.22329602776315996,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4413874662","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99759835,0.00022826844,0.001247483,0.000025463909,0.0000056969798,0.000009347881,0.00038680062,0.00008536645,0.00041319907],"genre_scores_gemma":[0.9969112,0.0001426973,0.0007660096,0.000025645508,0.0000023486007,0.00000760383,0.0009831834,0.000023927369,0.0011372786],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9999229,0.000010764102,0.000008897631,0.000025925325,0.000016537831,0.000014898255],"domain_scores_gemma":[0.9998851,0.000019552102,0.000038399332,0.000012845175,0.0000069715957,0.000037253096],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00010374088,0.0003044693,0.00013561179,0.00033703021,0.0001220869,0.00017471935,0.00015241651,0.00013260712,0.0006554883],"category_scores_gemma":[0.00009523948,0.00010017131,0.00016838522,0.00017852764,0.00014876669,0.000069726535,0.00017724419,0.00025889327,0.00018537787],"study_design_candidate":"bench_or_experimental","study_design_consensus":"bench_or_experimental","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.000057838224,0.000010119438,0.0006295956,0.000012794083,0.000004927627,0.00005356359,0.000014586089,0.000034774872,0.9983387,0.000028300557,0.0000112833,0.0008034443],"study_design_scores_gemma":[0.000045102966,0.00040741754,0.13398986,0.000016585906,0.00010342738,0.0011806766,0.00019177383,0.0029486727,0.85437095,0.0001551948,0.0065715373,0.00001873127],"about_ca_topic_score_codex":0.0013162988,"about_ca_topic_score_gemma":0.0030240042,"teacher_disagreement_score":0.0013162988,"about_ca_system_score_codex":0.00027988522,"about_ca_system_score_gemma":0.00015842897,"threshold_uncertainty_score":0.0026172996},"labels":[],"label_agreement":null},{"id":"W4414083996","doi":"10.1038/s41588-025-02357-1","title":"Author Correction: Why genomic diversity should not be framed by census alone","year":2025,"lang":"en","type":"erratum","venue":"Nature Genetics","topic":"Race, Genetics, and Society","field":"Biochemistry, Genetics and Molecular Biology","cited_by":0,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Genome Canada","funders":"","keywords":"Census; Diversity (politics); Genetic diversity; Genomics; American Community Survey","score_opus":0.013908657234443612,"score_gpt":0.2685041253993101,"score_spread":0.2545954681648665,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4414083996","genre_codex":"editorial","genre_gemma":"other","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"other","genre_consensus":null,"domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.000104230174,0.0004577158,0.0007559736,0.13347518,0.85821766,0.0000142546005,0.0011291394,0.00037392104,0.0054719117],"genre_scores_gemma":[0.012909714,0.00344386,0.0067613213,0.3009628,0.30564302,0.0002093615,0.0025583117,0.0032187442,0.36429286],"study_design_codex":"not_applicable","study_design_gemma":"not_applicable","domain_scores_codex":[0.99491864,0.0009224111,0.00070440565,0.0007963603,0.0022477654,0.0004103577],"domain_scores_gemma":[0.9516611,0.013970925,0.0016623138,0.0032377336,0.027398903,0.0020690728],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0056146695,0.0016331349,0.0015409434,0.0027143657,0.0040148613,0.0043178806,0.0027851942,0.0075970134,0.05132201],"category_scores_gemma":[0.09187539,0.001192672,0.0010493551,0.0021343415,0.0027723955,0.0029152648,0.0018919763,0.015861595,0.037023086],"study_design_candidate":"not_applicable","study_design_consensus":"not_applicable","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.000006980842,0.000001355742,0.000034573055,0.000015727732,0.0000027357505,0.00004876963,0.000015759082,0.000013111081,0.0000085453285,0.00066436024,0.99781114,0.0013768832],"study_design_scores_gemma":[0.0000289811,0.0000061768437,0.0005182653,0.00018867024,0.000019859182,0.00024923167,0.000099307086,0.00016587408,0.0001704131,0.0029869154,0.99553466,0.000031669068],"about_ca_topic_score_codex":0.043912135,"about_ca_topic_score_gemma":0.050383788,"teacher_disagreement_score":0.05132201,"about_ca_system_score_codex":0.0041161207,"about_ca_system_score_gemma":0.006206655,"threshold_uncertainty_score":0.17168921},"labels":[],"label_agreement":null},{"id":"W4414089767","doi":"10.1038/s41588-025-02307-x","title":"DNA methylation cooperates with genomic alterations during non-small cell lung cancer evolution","year":2025,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Epigenetics and DNA Methylation","field":"Biochemistry, Genetics and Molecular Biology","cited_by":7,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Canada's Michael Smith Genome Sciences Centre; University of British Columbia","funders":"Generalitat Valenciana; Wellcome Trust","keywords":"DNA methylation; Epigenetics; Gene; Chromatin; Illumina Methylation Assay; Bisulfite sequencing; Lung cancer; Methylation; DNA","score_opus":0.0036345192770358453,"score_gpt":0.2479736908474609,"score_spread":0.24433917157042506,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4414089767","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9993787,0.00009680093,0.00034101756,0.000010172789,4.2975557e-7,0.0000022873687,0.000028244627,0.0000042887677,0.00013797986],"genre_scores_gemma":[0.9996562,0.000026299213,0.00018132912,0.0000040567616,5.9604923e-7,0.000001508454,0.000059539587,0.0000020522662,0.00006845179],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99980956,0.00005728897,0.000013157212,0.0000430107,0.000044998455,0.0000319693],"domain_scores_gemma":[0.9997228,0.00008072109,0.0000925575,0.000024724017,0.000036095294,0.00004304898],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00034185857,0.000112756294,0.00020820068,0.00053217093,0.00016934518,0.0002851178,0.00015426347,0.00018350562,0.00038766974],"category_scores_gemma":[0.00065587787,0.0001009232,0.00014002141,0.00033390688,0.00020510427,0.000112207985,0.00022058112,0.00016229336,0.00008006692],"study_design_candidate":"bench_or_experimental","study_design_consensus":"bench_or_experimental","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00048606028,0.000027182923,0.46871617,0.000030473873,0.00006422185,0.0003241861,0.00024939282,0.00088881474,0.51943517,0.00025963582,0.00003686259,0.009481853],"study_design_scores_gemma":[0.0000066698153,0.00023157279,0.9530342,0.0000028792365,0.000029062872,0.000819946,0.00014315687,0.0026266603,0.042529706,0.00021040953,0.00035941892,0.0000062886033],"about_ca_topic_score_codex":0.0015417939,"about_ca_topic_score_gemma":0.0028006912,"teacher_disagreement_score":0.0015417939,"about_ca_system_score_codex":0.00029667298,"about_ca_system_score_gemma":0.0001591357,"threshold_uncertainty_score":0.0030656457},"labels":[],"label_agreement":null},{"id":"W4414111046","doi":"10.1038/s41588-025-02290-3","title":"The Solve-RD Solvathons as a pan-European interdisciplinary collaboration to diagnose patients with rare disease","year":2025,"lang":"en","type":"review","venue":"Nature Genetics","topic":"Genomics and Rare Diseases","field":"Biochemistry, Genetics and Molecular Biology","cited_by":4,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Children's Hospital of Eastern Ontario; University of Ottawa","funders":"Horizon 2020 Framework Programme; ZonMw; Deutsche Forschungsgemeinschaft; Generalitat de Catalunya; European Commission","keywords":"Multidisciplinary approach; Rare disease; Disease; Genome; Genetic diagnosis; Genomics; Best practice; Genetic testing; Medical diagnosis","score_opus":0.004458797293171494,"score_gpt":0.29494191402119985,"score_spread":0.29048311672802835,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4414111046","genre_codex":"review","genre_gemma":"review","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"review","genre_consensus":"review","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.00034046744,0.99071586,0.00067093724,0.0027690013,0.0013453547,0.000027333841,0.00008441599,0.000036327714,0.0040104454],"genre_scores_gemma":[0.004099492,0.9860772,0.0019097973,0.0035815889,0.0011462544,0.000069936,0.00036045746,0.000015125586,0.0027402302],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.99949145,0.00016419809,0.000049297632,0.000074316275,0.00013218712,0.00008851185],"domain_scores_gemma":[0.9991648,0.0003117987,0.0000764452,0.000019416519,0.0001986989,0.00022884546],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.001958944,0.0009396246,0.0010067079,0.0013347549,0.00030727134,0.0011233767,0.0009795327,0.0018076985,0.006000162],"category_scores_gemma":[0.00180597,0.00015907489,0.0006899287,0.0010229821,0.0003911915,0.00088476477,0.001740189,0.0023180633,0.0025742378],"study_design_candidate":"not_applicable","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00019640484,0.00007582437,0.00052562915,0.005936688,0.00019971516,0.00031905778,0.000044953806,0.000242526,0.0005748046,0.0038001197,0.07289615,0.91518813],"study_design_scores_gemma":[0.00025881163,0.00015670393,0.002375774,0.009698659,0.00034412995,0.0017076388,0.00009373383,0.00014774162,0.00033531192,0.0021748426,0.9826804,0.000026230868],"about_ca_topic_score_codex":0.0011971565,"about_ca_topic_score_gemma":0.0034613914,"teacher_disagreement_score":0.006000162,"about_ca_system_score_codex":0.0008988621,"about_ca_system_score_gemma":0.002409682,"threshold_uncertainty_score":0.02007252},"labels":[],"label_agreement":null},{"id":"W4414335677","doi":"10.1038/s41588-025-02301-3","title":"Genetic and epigenetic screens in primary human T cells link candidate causal autoimmune variants to T cell networks","year":2025,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Diabetes and associated disorders","field":"Biochemistry, Genetics and Molecular Biology","cited_by":6,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of British Columbia","funders":"National Institute of Diabetes and Digestive and Kidney Diseases; National Institute of Allergy and Infectious Diseases; Michael Smith Health Research BC; National Human Genome Research Institute; Canadian Network for Research and Innovation in Machining Technology, Natural Sciences and Engineering Research Council of Canada; National Institute on Aging; Crohn's and Colitis Foundation","keywords":"Gene; T cell; Epigenetics; Autoimmune disease; Gene expression; Regulation of gene expression; Disease","score_opus":0.002361817945874929,"score_gpt":0.21830694338807888,"score_spread":0.21594512544220396,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4414335677","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9805706,0.00073787686,0.015098457,0.00009489215,0.000024719302,0.00003999403,0.0016473674,0.0003101845,0.0014758543],"genre_scores_gemma":[0.9901287,0.0003736314,0.0074497196,0.00009146509,0.000008744234,0.000033531043,0.0010839768,0.000048973285,0.0007812355],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99968505,0.000042596184,0.000022629654,0.00011787279,0.0000866401,0.000045177567],"domain_scores_gemma":[0.99977654,0.000093977455,0.00005698847,0.000029560268,0.000014728767,0.000028189419],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00023366458,0.00038143553,0.00031908829,0.0003942575,0.00020203194,0.00034824666,0.0002143845,0.0002763349,0.0022031895],"category_scores_gemma":[0.00034373064,0.00015139897,0.00045932515,0.00037644923,0.00027044694,0.00010229459,0.00032777767,0.00054378185,0.00029260022],"study_design_candidate":"bench_or_experimental","study_design_consensus":"bench_or_experimental","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.000112782356,0.000017640328,0.0023704707,0.00004703504,0.000045297824,0.000133455,0.00001931931,0.00037960583,0.99346125,0.00014845787,0.00005617714,0.00320866],"study_design_scores_gemma":[0.000045371173,0.0005263864,0.054061692,0.000015720165,0.00028050496,0.0013295867,0.00006822559,0.004271473,0.9353185,0.00050343276,0.003560372,0.000018638199],"about_ca_topic_score_codex":0.00058228866,"about_ca_topic_score_gemma":0.001768356,"teacher_disagreement_score":0.0022031895,"about_ca_system_score_codex":0.000231926,"about_ca_system_score_gemma":0.00016593607,"threshold_uncertainty_score":0.0073704123},"labels":[],"label_agreement":null},{"id":"W4414394134","doi":"10.1038/s41588-025-02325-9","title":"Bryophytes hold a larger gene family space than vascular plants","year":2025,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Bryophyte Studies and Records","field":"Agricultural and Biological Sciences","cited_by":30,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Université Laval","funders":"","keywords":"Bryophyte; Horizontal gene transfer; Gene; Gene family; Genetic diversity; Extant taxon; Vascular plant","score_opus":0.0073012922467133425,"score_gpt":0.21415073218723488,"score_spread":0.20684943994052155,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4414394134","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9538565,0.014502294,0.010924717,0.00046558477,0.00005123257,0.000012695289,0.0132360775,0.00035282644,0.0065980963],"genre_scores_gemma":[0.9537319,0.0062942845,0.008904262,0.00028492292,0.000043687844,0.000041645944,0.027497988,0.00010166935,0.0030996995],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.999813,0.000020274536,0.000009413728,0.000095433556,0.000029358778,0.000032601347],"domain_scores_gemma":[0.99973446,0.000049013128,0.00008158457,0.000039939234,0.000030601568,0.000064255466],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00023104956,0.00027320205,0.00053101167,0.00092234847,0.0007910195,0.00080125744,0.00027705746,0.00021937072,0.004905555],"category_scores_gemma":[0.00029130702,0.00015097829,0.00033323397,0.0024402796,0.0003124838,0.00075806846,0.00058858463,0.00040282225,0.001253119],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00079925865,0.000083737825,0.16350314,0.00097548787,0.00038678478,0.0010262313,0.0021542849,0.0008598878,0.62264895,0.008201532,0.003940497,0.1954202],"study_design_scores_gemma":[0.00003423103,0.0001868084,0.75006276,0.00014490342,0.00025378502,0.0024186238,0.0019762318,0.0010778187,0.016795756,0.0048620333,0.22211264,0.00007436197],"about_ca_topic_score_codex":0.0027119017,"about_ca_topic_score_gemma":0.0049691787,"teacher_disagreement_score":0.004905555,"about_ca_system_score_codex":0.0003001756,"about_ca_system_score_gemma":0.00037492695,"threshold_uncertainty_score":0.016410708},"labels":[],"label_agreement":null},{"id":"W4415024972","doi":"10.1038/s41588-025-02364-2","title":"Population-scale gene-based analysis of whole-genome sequencing provides insights into metabolic health","year":2025,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Genomics and Rare Diseases","field":"Biochemistry, Genetics and Molecular Biology","cited_by":4,"is_retracted":false,"has_abstract":true,"route_ca_aff":false,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"","funders":"Medical Research Council; Queen's University; Queen's University Belfast; University of Bristol; National Institute for Health and Care Research; Wellcome Trust; University of North Carolina at Chapel Hill; National Institutes of Health; U.S. Department of Health and Human Services","keywords":"Exome sequencing; Type 2 diabetes; Exome; Biobank; Gene; Genome; DNA sequencing; Genome-wide association study; Disease","score_opus":0.005753594763842021,"score_gpt":0.26528595698970453,"score_spread":0.2595323622258625,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4415024972","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.94823956,0.001183391,0.03438443,0.00041662692,0.00005394451,0.000031859,0.012218517,0.00021452786,0.0032572132],"genre_scores_gemma":[0.98778915,0.0004703484,0.006179062,0.00020307467,0.000032564814,0.000024974359,0.0045041908,0.000057251116,0.0007393331],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9993988,0.0002733039,0.000029284103,0.00019197485,0.0000740684,0.00003247866],"domain_scores_gemma":[0.9987728,0.0005387743,0.00024864747,0.00028496564,0.000086547014,0.000068290545],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0015532604,0.00034388568,0.00038412542,0.0011949366,0.00020559435,0.0007100993,0.000261744,0.00033884714,0.002382304],"category_scores_gemma":[0.0023705857,0.00015885691,0.00046968,0.0015293631,0.00029623462,0.00029610726,0.0005309069,0.00046896597,0.00043816504],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0004801622,0.00008453322,0.8336645,0.00025720455,0.0027852396,0.0004805812,0.00030687303,0.005426351,0.10352127,0.0018130277,0.0030612254,0.048119046],"study_design_scores_gemma":[0.000019160992,0.00008850082,0.97726166,0.00003929219,0.00037036833,0.00054938754,0.00019138868,0.006688501,0.0056190337,0.0023786484,0.0067767757,0.00001737066],"about_ca_topic_score_codex":0.00259448,"about_ca_topic_score_gemma":0.0037573355,"teacher_disagreement_score":0.00259448,"about_ca_system_score_codex":0.00014593337,"about_ca_system_score_gemma":0.00016613316,"threshold_uncertainty_score":0.008214533},"labels":[],"label_agreement":null},{"id":"W4415361592","doi":"10.1038/s41588-025-02333-9","title":"Shifted assembly and function of mSWI/SNF family subcomplexes underlie targetable dependencies in dedifferentiated endometrial carcinomas","year":2025,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Chromatin Remodeling and Cancer","field":"Biochemistry, Genetics and Molecular Biology","cited_by":2,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of British Columbia","funders":"National Institute of General Medical Sciences; National Institutes of Health; Terry Fox Research Institute; U.S. Department of Health and Human Services; Howard Hughes Medical Institute","keywords":"Chromatin; ARID1A; SMARCA4; Chromatin remodeling; Function (biology); Cell growth; Gene; Cancer; Regulation of gene expression; Endometrial cancer","score_opus":0.011723136168823695,"score_gpt":0.25896245816450597,"score_spread":0.24723932199568227,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4415361592","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.998464,0.0002541592,0.00068520516,0.000021069764,0.000003965065,0.0000039762363,0.00017074154,0.000029714263,0.00036725702],"genre_scores_gemma":[0.9987618,0.0000859008,0.00022968788,0.000013023928,0.0000017552295,0.000004324563,0.00021519476,0.0000145867325,0.00067360786],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9998398,0.000015065205,0.000024071396,0.000034955836,0.000046865112,0.000039256352],"domain_scores_gemma":[0.9997687,0.000044752083,0.000048426857,0.00005608765,0.000031186977,0.000050880888],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00022532589,0.00018953497,0.00021580656,0.00051594834,0.00016227295,0.0005221103,0.0002892728,0.00023590673,0.001892878],"category_scores_gemma":[0.0003499852,0.00028080255,0.0002137752,0.00023934363,0.00026609705,0.00024398424,0.00041236886,0.00036428295,0.00041892508],"study_design_candidate":"bench_or_experimental","study_design_consensus":"bench_or_experimental","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00020080263,0.00001286615,0.0049252375,0.000016795913,0.000012086514,0.00017320176,0.00004908155,0.000119763245,0.9928582,0.00024318842,0.000040122737,0.0013486227],"study_design_scores_gemma":[0.000018495444,0.000097949836,0.19299145,0.000005731567,0.000037214886,0.0015226596,0.0002978466,0.002348636,0.7997638,0.00033504213,0.002569308,0.00001185759],"about_ca_topic_score_codex":0.00088915776,"about_ca_topic_score_gemma":0.0010143361,"teacher_disagreement_score":0.001892878,"about_ca_system_score_codex":0.00034845623,"about_ca_system_score_gemma":0.00013076357,"threshold_uncertainty_score":0.0063322783},"labels":[],"label_agreement":null},{"id":"W4415407332","doi":"10.1038/s41588-025-02361-5","title":"Pathogenic UNC13A variants cause a neurodevelopmental syndrome by impairing synaptic function","year":2025,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Genetics, Aging, and Longevity in Model Organisms","field":"Biochemistry, Genetics and Molecular Biology","cited_by":3,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Alberta Children's Hospital; University of Calgary; Centre Hospitalier Universitaire Sainte-Justine; BC Children's Hospital; Université de Montréal; University of Alberta; University of British Columbia; Hospital for Sick Children","funders":"National Institute of Neurological Disorders and Stroke; Einstein Stiftung Berlin; Deutsche Forschungsgemeinschaft; U.S. Department of Health and Human Services; National Institutes of Health; Indian Council of Medical Research; Target ALS; National Human Genome Research Institute; Wellcome Trust; National Health and Medical Research Council; State Government of Victoria; Japan Agency for Medical Research and Development; Eesti Teadusagentuur","keywords":"Neurotransmission; Neurotransmitter; Caenorhabditis elegans; Hippocampal formation; Loss function; Gene; Neurotransmitter Agents; Nervous system; Germline","score_opus":0.004543413473788443,"score_gpt":0.22147882868351293,"score_spread":0.21693541520972448,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4415407332","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9920033,0.0010940919,0.004956689,0.000055692522,0.000016636699,0.000022311651,0.0006063201,0.0002064086,0.0010385318],"genre_scores_gemma":[0.9951748,0.00054144725,0.0034277416,0.000031683532,0.0000040196824,0.000012867069,0.00026774482,0.000022548944,0.00051710213],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9998503,0.000015942178,0.000029042902,0.000038585393,0.000047749127,0.00001833534],"domain_scores_gemma":[0.99982685,0.00003126992,0.00007253845,0.0000138388605,0.000019354557,0.000036149006],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00008699117,0.0010969694,0.00023786831,0.0007311759,0.00024904558,0.000192425,0.00023749372,0.0003936525,0.00086363126],"category_scores_gemma":[0.00028118832,0.00014138789,0.00025696697,0.0003807086,0.00036695792,0.00012247448,0.0003772457,0.00027279265,0.00026658844],"study_design_candidate":"bench_or_experimental","study_design_consensus":"bench_or_experimental","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0002984505,0.000028598899,0.02187455,0.00006625636,0.000080764934,0.0063415198,0.000069140304,0.00044057652,0.96079016,0.00060630974,0.00028104315,0.009122671],"study_design_scores_gemma":[0.00005460192,0.00055677944,0.2566826,0.000088010194,0.00019103306,0.0492367,0.00024115057,0.0033371216,0.6827331,0.001311677,0.0055221133,0.000045094268],"about_ca_topic_score_codex":0.0019487453,"about_ca_topic_score_gemma":0.0031376446,"teacher_disagreement_score":0.0019487453,"about_ca_system_score_codex":0.0002082509,"about_ca_system_score_gemma":0.00021003005,"threshold_uncertainty_score":0.0038748384},"labels":[],"label_agreement":null},{"id":"W4415656346","doi":"10.1038/s41588-025-02368-y","title":"Cell-type- and locus-specific epigenetic editing of memory expression","year":2025,"lang":"en","type":"article","venue":"Nature Genetics","topic":"CRISPR and Genetic Engineering","field":"Biochemistry, Genetics and Molecular Biology","cited_by":8,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Toronto","funders":"Schweizerischer Nationalfonds zur Förderung der Wissenschaftlichen Forschung","keywords":"Epigenetics; Epigenesis; Engram; Epigenetic regulation of neurogenesis; Regulator; Master regulator; Regulation of gene expression","score_opus":0.003453597764858766,"score_gpt":0.26723735004757154,"score_spread":0.2637837522827128,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4415656346","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.8787984,0.002233889,0.10676776,0.00027309541,0.00026235142,0.0000844543,0.00077963725,0.001325186,0.0094753215],"genre_scores_gemma":[0.9836511,0.0004684129,0.011088532,0.0000828415,0.000024428004,0.000033645414,0.00024421682,0.00018272427,0.004224133],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9997739,0.00001669923,0.000017222486,0.000089165944,0.00006112794,0.000041778883],"domain_scores_gemma":[0.9997062,0.000061466526,0.000094641866,0.000082471306,0.000021998021,0.000033155855],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00025934115,0.00030180812,0.00025801305,0.00022576674,0.00011992851,0.00044901553,0.0004422514,0.00024356818,0.002008116],"category_scores_gemma":[0.00029121176,0.0001356387,0.00026140956,0.0001158769,0.0004351825,0.00029501252,0.0006353587,0.0007356728,0.0004980025],"study_design_candidate":"bench_or_experimental","study_design_consensus":"bench_or_experimental","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00001982593,0.000011520245,0.00013949863,0.00002319547,0.000004720911,0.000035253794,0.000011295183,0.000101565456,0.99597603,0.0006299944,0.000028812576,0.003018218],"study_design_scores_gemma":[0.0000031087145,0.000054199347,0.00091207714,0.00000348304,0.000009233042,0.0001295537,0.000008139984,0.00082385784,0.9957338,0.00016979352,0.0021492427,0.000003554783],"about_ca_topic_score_codex":0.00018341378,"about_ca_topic_score_gemma":0.00041748086,"teacher_disagreement_score":0.002008116,"about_ca_system_score_codex":0.00019318258,"about_ca_system_score_gemma":0.00016123387,"threshold_uncertainty_score":0.006717801},"labels":[],"label_agreement":null},{"id":"W4416188565","doi":"10.1038/s41588-025-02396-8","title":"Genome-wide association analyses identify distinct genetic architectures for early-onset and late-onset depression","year":2025,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Genetic Associations and Epidemiology","field":"Biochemistry, Genetics and Molecular Biology","cited_by":6,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Manitoba","funders":"National Institute of Mental Health; AstraZeneca; Tartu Ülikool; Forskningsrådet om Hälsa, Arbetsliv och Välfärd; Stiftelsen för Strategisk Forskning; Genentech; Norges Forskningsråd; Business Finland; Universitetet i Oslo; Vetenskapsrådet; NordForsk; Karolinska Institutet; Helse- og Omsorgsdepartementet; Uppsala Multidisciplinary Center for Advanced Computational Science; Eesti Teadusagentuur; Maze Therapeutics; European Regional Development Fund; European Commission; Sanofi; Celgene; Pfizer; Biogen; GlaxoSmithKline; Bristol-Myers Squibb","keywords":"Biobank; Genetic architecture; Polygenic risk score; Major depressive disorder; Decile; Depression (economics); Genetic association; Genome-wide association study; Identification (biology)","score_opus":0.010563680476551703,"score_gpt":0.3210241039196785,"score_spread":0.3104604234431268,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4416188565","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9980551,0.00038231452,0.0007976349,0.000080334205,0.0000070591464,0.000005622173,0.00033923006,0.000009765126,0.00032300362],"genre_scores_gemma":[0.999265,0.000084880536,0.00036247983,0.000018959323,0.0000041820444,0.0000027334522,0.00017490625,0.000002436949,0.00008445437],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9992964,0.00031805274,0.000067577086,0.000178962,0.00006601468,0.00007301991],"domain_scores_gemma":[0.9985607,0.0005293045,0.00056961004,0.00012504488,0.00008234264,0.00013291475],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0008986241,0.00028223527,0.00026781022,0.0011392637,0.0003055053,0.0006436411,0.00029769354,0.0003879799,0.0014778114],"category_scores_gemma":[0.0021023043,0.00019020808,0.00056881626,0.0008615067,0.00036559647,0.00016385905,0.00053420814,0.0005879603,0.00011771675],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00029233898,0.00003633957,0.99062914,0.000014208405,0.00034138878,0.00022208331,0.000081809274,0.00024162041,0.004751517,0.00018028285,0.00013898454,0.0030702672],"study_design_scores_gemma":[0.000010340371,0.000034139124,0.99862695,0.000008473323,0.0000765351,0.00019255625,0.000071091206,0.00044758525,0.0002773352,0.00016198108,0.0000898103,0.0000033215413],"about_ca_topic_score_codex":0.0041321646,"about_ca_topic_score_gemma":0.00816042,"teacher_disagreement_score":0.0041321646,"about_ca_system_score_codex":0.00018764475,"about_ca_system_score_gemma":0.0002555755,"threshold_uncertainty_score":0.008216202},"labels":[{"model":"gemma","categories":[],"domain":null,"study_design":"observational","genre":"empirical","about_ca_system":false,"about_ca_topic":false,"confidence":"high"},{"model":"gpt","categories":[],"domain":null,"study_design":"observational","genre":"empirical","about_ca_system":false,"about_ca_topic":false,"confidence":"high"}],"label_agreement":"agree"},{"id":"W4416599612","doi":"10.1038/s41588-025-02400-1","title":"Proteome-wide model for human disease genetics","year":2025,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Genomics and Rare Diseases","field":"Biochemistry, Genetics and Molecular Biology","cited_by":18,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Artificial Intelligence in Medicine (Canada)","funders":"National Cancer Institute; National Institutes of Health; National Science Foundation; Generalitat de Catalunya; Agencia Estatal de Investigación; Invitae; Ministerio de Ciencia e Innovación; Centres de Recerca de Catalunya","keywords":"Disease; Missense mutation; Limiting; Population; Human disease; Human genetic variation; Generative grammar; Medical genetics; Human genetics","score_opus":0.007377347058354692,"score_gpt":0.2790728267176209,"score_spread":0.2716954796592662,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4416599612","genre_codex":"methods","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":null,"domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.06097411,0.0019932415,0.919498,0.002766798,0.00021979031,0.00010931226,0.006678398,0.0025174513,0.0052428823],"genre_scores_gemma":[0.8110815,0.002169272,0.15848571,0.0018966813,0.00033755825,0.00061378063,0.01004819,0.00063653797,0.014730819],"study_design_codex":"simulation_or_modeling","study_design_gemma":"simulation_or_modeling","domain_scores_codex":[0.9994454,0.00022410294,0.000018264367,0.00019624026,0.000066807515,0.00004919636],"domain_scores_gemma":[0.99890566,0.0007205565,0.00008488862,0.000105379346,0.00011801792,0.00006549145],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.001994797,0.0008675994,0.0010608238,0.0010322994,0.00041812874,0.0012762886,0.0018192441,0.0016695053,0.0053710374],"category_scores_gemma":[0.0058732843,0.0005143571,0.001348305,0.0011598422,0.0009850815,0.0011531987,0.001282116,0.0020774996,0.0014954603],"study_design_candidate":"simulation_or_modeling","study_design_consensus":"simulation_or_modeling","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00015821838,0.00005397549,0.007010017,0.00010219293,0.00023059528,0.0003305293,0.00010550145,0.88491076,0.0015655078,0.06559992,0.008157257,0.031775527],"study_design_scores_gemma":[0.000023033681,0.000012803044,0.0008172378,0.000011540187,0.000022503904,0.00008434495,0.000007756467,0.93620557,0.0001444833,0.060798716,0.0018595369,0.000012411289],"about_ca_topic_score_codex":0.0090853805,"about_ca_topic_score_gemma":0.009102203,"teacher_disagreement_score":0.0090853805,"about_ca_system_score_codex":0.0012474105,"about_ca_system_score_gemma":0.0011755751,"threshold_uncertainty_score":0.018065035},"labels":[],"label_agreement":null},{"id":"W4416735647","doi":"10.1038/s41588-025-02413-w","title":"A genome-wide association study of mass spectrometry proteomics using a nanoparticle enrichment platform","year":2025,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Genetic Associations and Epidemiology","field":"Biochemistry, Genetics and Molecular Biology","cited_by":6,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Cytodiagnostics (Canada)","funders":"National Institute of Allergy and Infectious Diseases; Qatar National Research Fund; U.S. Department of Health and Human Services; National Institutes of Health; National Heart, Lung, and Blood Institute; Fonds National de la Recherche Luxembourg; Qatar Foundation","keywords":"Proteomics; Quantitative proteomics; Mass spectrometry; Epitope; Gene isoform; Proteome; Complement (music)","score_opus":0.009652383070086172,"score_gpt":0.27690796458487316,"score_spread":0.267255581514787,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4416735647","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99200386,0.00044736228,0.0062203463,0.00013447586,0.000030744995,0.000034621207,0.0005308717,0.00004868345,0.00054899545],"genre_scores_gemma":[0.9938391,0.0001526827,0.0050958875,0.00010991021,0.000016737988,0.000036061527,0.00039103004,0.000015666601,0.00034298544],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99782324,0.00080088724,0.000130741,0.00079468236,0.0003355029,0.00011497223],"domain_scores_gemma":[0.99841917,0.00072025403,0.000265331,0.00031046887,0.00017476037,0.000110045105],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0023277502,0.00045832098,0.0004124563,0.00088925776,0.0005733313,0.0007081132,0.00033769986,0.0007785974,0.00079464144],"category_scores_gemma":[0.0034760367,0.0002902779,0.0007670602,0.0011938057,0.00032502066,0.00021416467,0.00043788154,0.00057308545,0.00016757603],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0024794636,0.00023562314,0.82351357,0.00014488507,0.0032131241,0.0015010673,0.0003882869,0.0005273957,0.1499045,0.0006021716,0.0006270752,0.016862864],"study_design_scores_gemma":[0.00007797402,0.0006899636,0.98098594,0.000010811203,0.0011976729,0.001970186,0.000093713774,0.0024013729,0.010427165,0.00026645415,0.0018543847,0.000024414381],"about_ca_topic_score_codex":0.0027870038,"about_ca_topic_score_gemma":0.0035207525,"teacher_disagreement_score":0.0027870038,"about_ca_system_score_codex":0.00021346867,"about_ca_system_score_gemma":0.0003609355,"threshold_uncertainty_score":0.012310505},"labels":[],"label_agreement":null},{"id":"W4417208816","doi":"10.1038/s41588-025-02447-0","title":"A call for a global cyberbiosecurity framework in genomics","year":2025,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Law, AI, and Intellectual Property","field":"Computer Science","cited_by":0,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"McGill University; McGill University and Génome Québec Innovation Centre; McGill Genome Centre","funders":"Canadian Institutes of Health Research","keywords":"Genomics; Geopolitics; Corporate governance; Global governance; Population genomics; Safeguard; Structural genomics","score_opus":0.00975282184869505,"score_gpt":0.27320699683241706,"score_spread":0.26345417498372203,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4417208816","genre_codex":"commentary","genre_gemma":"commentary","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"commentary","genre_consensus":"commentary","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.00729607,0.008960405,0.097241275,0.74738306,0.004340026,0.00006667551,0.00015207156,0.00046121023,0.13409923],"genre_scores_gemma":[0.58216053,0.009347141,0.10855135,0.25288928,0.010984672,0.0006805113,0.00030357964,0.0005915884,0.03449137],"study_design_codex":"theoretical_or_conceptual","study_design_gemma":"not_applicable","domain_scores_codex":[0.9908371,0.0045834053,0.00028028514,0.0012996988,0.0020057466,0.0009938393],"domain_scores_gemma":[0.96860147,0.017021757,0.0010806764,0.005717839,0.0030338904,0.004544395],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.03406995,0.0008753768,0.0014645333,0.0023243364,0.004972691,0.0143850325,0.0034528214,0.01748213,0.012220398],"category_scores_gemma":[0.024995258,0.00060186203,0.0014754778,0.0013916144,0.045222457,0.02714896,0.0109387515,0.021331804,0.0016456407],"study_design_candidate":"not_applicable","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.000009676248,0.000013592238,0.0000777953,0.000022556042,0.000006390695,0.000024365647,0.00019659896,0.00039470184,0.000101167956,0.9892749,0.0055185184,0.004359745],"study_design_scores_gemma":[0.000012168687,0.000014615897,0.0001157003,0.00007811662,0.0000045689667,0.000024737576,0.0002385793,0.0004809538,0.00008151494,0.9517294,0.047206197,0.000013389463],"about_ca_topic_score_codex":0.004151031,"about_ca_topic_score_gemma":0.0035974,"teacher_disagreement_score":0.03406995,"about_ca_system_score_codex":0.0066249063,"about_ca_system_score_gemma":0.012123812,"threshold_uncertainty_score":0.18018132},"labels":[],"label_agreement":null},{"id":"W4417492474","doi":"10.1038/s41588-025-02417-6","title":"Genomic and transcriptomic analyses of aortic stenosis enhance therapeutic target discovery and disease prediction","year":2025,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Genetic Associations and Epidemiology","field":"Biochemistry, Genetics and Molecular Biology","cited_by":6,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Ottawa; Université Laval; Institut universitaire de cardiologie et de pneumologie de Québec; McGill University; McGill University Health Centre","funders":"Fonds de Recherche du Québec - Santé; Canadian Institutes of Health Research; Heart and Stroke Foundation of Canada","keywords":"Transcriptome; Locus (genetics); Disease; Quantitative trait locus; Genome-wide association study; Gene; Expression quantitative trait loci; Genetic association","score_opus":0.009099226252393738,"score_gpt":0.2933058512874754,"score_spread":0.28420662503508165,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4417492474","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9578113,0.012837952,0.019335916,0.0014092493,0.00009555849,0.000060228685,0.0048314133,0.00021703479,0.0034013505],"genre_scores_gemma":[0.9878044,0.0024492647,0.007334209,0.00033017874,0.00008771949,0.00002928399,0.0014441956,0.000025156272,0.000495566],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99949765,0.00017488575,0.00003840089,0.00014517203,0.000088404086,0.0000554901],"domain_scores_gemma":[0.99913424,0.0003804676,0.00027713602,0.00008126327,0.00006591446,0.00006106908],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0011109277,0.0003865912,0.0005506418,0.0013122658,0.0002342057,0.00083962275,0.00019405229,0.00041324657,0.0015118791],"category_scores_gemma":[0.0015842747,0.00020165819,0.0006233996,0.0012553756,0.00029447215,0.00029314804,0.00045266587,0.0005235508,0.0002486401],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0018786745,0.00021954672,0.6405917,0.0008077948,0.0022392997,0.0004888643,0.00019044559,0.005399616,0.2288647,0.0016821652,0.002007705,0.11562955],"study_design_scores_gemma":[0.00015587275,0.0005975772,0.9445547,0.00010975137,0.0022450408,0.00069866655,0.0002475362,0.014505348,0.01983725,0.008327794,0.008675654,0.00004474833],"about_ca_topic_score_codex":0.0007750682,"about_ca_topic_score_gemma":0.0016334227,"teacher_disagreement_score":0.0015118791,"about_ca_system_score_codex":0.0002155187,"about_ca_system_score_gemma":0.00034429197,"threshold_uncertainty_score":0.00587523},"labels":[],"label_agreement":null},{"id":"W7116773052","doi":"10.1038/s41588-025-02420-x","title":"Patterns of hypermutation shape tumorigenesis and immunotherapy response in mismatch-repair-deficient glioma","year":2025,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Glioma Diagnosis and Treatment","field":"Medicine","cited_by":2,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"SickKids Foundation; University of Toronto; Sinai Health System; Princess Margaret Cancer Centre; Stollery Children's Hospital; Hospital for Sick Children","funders":"","keywords":"Somatic hypermutation; Glioma; Immunotherapy; Carcinogenesis; Mutation; Point mutation; DNA methylation; Mutagenesis","score_opus":0.007686176007489216,"score_gpt":0.28126259450518015,"score_spread":0.27357641849769093,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W7116773052","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9988752,0.00020983184,0.0003763391,0.00002062526,0.000002098072,0.0000027875426,0.00013431504,0.00002476507,0.0003539302],"genre_scores_gemma":[0.99925786,0.00007909695,0.00018618983,0.00001603272,0.0000014552928,0.0000025977988,0.00011992738,0.000019403775,0.00031749712],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9998623,0.000018302628,0.000011494209,0.000033827077,0.000038662507,0.00003552201],"domain_scores_gemma":[0.9997428,0.000056659555,0.00010906761,0.000026330805,0.000028072895,0.000037009748],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00014199832,0.0001214037,0.00022423692,0.00057588785,0.00009504659,0.0004751001,0.0001571104,0.00027829167,0.0019364919],"category_scores_gemma":[0.0005468719,0.00018004447,0.00015725967,0.00035066134,0.00016590727,0.00026810708,0.0002063658,0.0002899587,0.00040670062],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0014976646,0.0000800211,0.09063436,0.000041659714,0.00007082354,0.00014645534,0.000087909284,0.0014604237,0.8893114,0.00041855228,0.00027863917,0.015972164],"study_design_scores_gemma":[0.000029032291,0.00060919905,0.7868755,0.000012324598,0.00007032287,0.002143557,0.00026132775,0.0086333165,0.19848314,0.0009920647,0.0018629264,0.000027263119],"about_ca_topic_score_codex":0.00046729104,"about_ca_topic_score_gemma":0.0006411933,"teacher_disagreement_score":0.0019364919,"about_ca_system_score_codex":0.00024211555,"about_ca_system_score_gemma":0.00010030704,"threshold_uncertainty_score":0.00647825},"labels":[],"label_agreement":null},{"id":"W7116978255","doi":"10.1038/s41588-025-02441-6","title":"Designing synthetic regulatory elements using the generative AI framework DNA-Diffusion","year":2025,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Genomics and Chromatin Dynamics","field":"Biochemistry, Genetics and Molecular Biology","cited_by":8,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Mila - Quebec Artificial Intelligence Institute","funders":"National Institutes of Health","keywords":"Generative grammar; Synthetic biology; Genomics; Regulatory sequence; Computational genomics; Functional genomics; Gene regulatory network; Gene; Regulation of gene expression","score_opus":0.005375264760373992,"score_gpt":0.2607968145849224,"score_spread":0.2554215498245484,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W7116978255","genre_codex":"methods","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":null,"domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.06929547,0.00022322992,0.91484696,0.00025681208,0.00012420314,0.000113744245,0.000060994204,0.0011248296,0.013953766],"genre_scores_gemma":[0.7119792,0.00033155113,0.2793785,0.00017833315,0.00002449121,0.0002690223,0.000118156655,0.00044874803,0.0072719343],"study_design_codex":"theoretical_or_conceptual","study_design_gemma":"simulation_or_modeling","domain_scores_codex":[0.9997098,0.00007526798,0.000014285143,0.00007615384,0.00008744554,0.00003704369],"domain_scores_gemma":[0.99949145,0.00033182406,0.000031632284,0.00006786012,0.000040457187,0.000036809015],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0005740293,0.00045002828,0.0004669925,0.00033436625,0.00047428542,0.0007279838,0.0011082665,0.0006781834,0.0036712547],"category_scores_gemma":[0.0014486127,0.0004040489,0.0005031166,0.00032509692,0.0008596093,0.0006472492,0.00094734726,0.0012617392,0.0007887769],"study_design_candidate":"simulation_or_modeling","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00022526167,0.0001489435,0.00072086276,0.00036801444,0.000048132326,0.00023045477,0.00042854119,0.2412612,0.19576372,0.49754602,0.0009812156,0.06227769],"study_design_scores_gemma":[0.00009192848,0.00020915832,0.00013245645,0.00003392989,0.0000349012,0.0001458208,0.00011146253,0.7588439,0.106937796,0.114453204,0.018954562,0.000050932562],"about_ca_topic_score_codex":0.0005463442,"about_ca_topic_score_gemma":0.0006826402,"teacher_disagreement_score":0.0036712547,"about_ca_system_score_codex":0.0006591669,"about_ca_system_score_gemma":0.00043641345,"threshold_uncertainty_score":0.012281597},"labels":[],"label_agreement":null}]}