{"meta":{"query_hash":"dd054e9cb202","filters":{"topic":"Genetic Syndromes and Imprinting"},"cohort_total":808,"direct_labels_cover":1,"predictions_cover":808,"exported":808,"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/dd054e9cb202","api":"https://metacan.xera.ac/api/v1/cohort?topic=Genetic+Syndromes+and+Imprinting"},"results":[{"id":"W1481125586","doi":"10.1002/stem.1405","title":"Zac1 Regulates Astroglial Differentiation of Neural Stem Cells Through <i>Socs3</i>","year":2013,"lang":"en","type":"article","venue":"Stem Cells","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":25,"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 Science Council; University of Toronto; Deutsche Forschungsgemeinschaft; University of Cambridge","keywords":"Biology; Neural stem cell; Cell biology; SOCS3; Embryonic stem cell; Cellular differentiation; Gene knockdown; STAT3; Stem cell; Signal transduction; Apoptosis; Gene; Genetics","score_opus":0.009138094209769049,"score_gpt":0.20363846561396384,"score_spread":0.1945003714041948,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1481125586","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9900122,0.0032299664,0.0032161714,0.00017103589,0.000037595975,0.00002179433,0.0007875808,0.00030277384,0.0022207405],"genre_scores_gemma":[0.9956564,0.0011601262,0.0011747197,0.00007120331,0.000008056977,0.000026717646,0.00051389105,0.000030810683,0.001358095],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9999186,0.000009206968,0.000006768706,0.000016960825,0.000018482171,0.00003001618],"domain_scores_gemma":[0.99993575,0.0000047232325,0.00003001976,0.0000039094994,0.0000072499224,0.000018298966],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0000707043,0.00040110422,0.00017899452,0.00023880569,0.00024168448,0.00033750467,0.00015169289,0.0001602861,0.00090765045],"category_scores_gemma":[0.00007503696,0.00013345666,0.00023090663,0.00013412285,0.0003308052,0.00013726835,0.00020734407,0.00046869493,0.0002904066],"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":[0.00008671323,0.0000067644196,0.00032992626,0.00003701571,0.000003956986,0.0000249919,0.0000107323995,0.00009097779,0.998131,0.00016594086,0.00007642869,0.001035598],"study_design_scores_gemma":[0.000025684538,0.00010049125,0.015224241,0.000008948209,0.000028938168,0.00010513771,0.000030705323,0.0019238676,0.97883135,0.000083137784,0.0036307226,0.000006767171],"about_ca_topic_score_codex":0.0020946306,"about_ca_topic_score_gemma":0.004464782,"teacher_disagreement_score":0.0020946306,"about_ca_system_score_codex":0.0005826139,"about_ca_system_score_gemma":0.00046109728,"threshold_uncertainty_score":0.004227221},"labels":[],"label_agreement":null},{"id":"W1483213138","doi":"10.1016/s1937-6448(09)76005-8","title":"Chapter 5 Imprinting and Extraembryonic Tissues—Mom Takes Control","year":2009,"lang":"en","type":"review","venue":"International review of cell and molecular biology","topic":"Genetic Syndromes and Imprinting","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; Neuroectoderm; Genomic imprinting; Endoderm; Imprinting (psychology); Yolk sac; Gastrulation; Placentation; Epigenetics; Genetics; Cell biology; Embryonic stem cell; Body plan; Zebrafish; Mesoderm; Embryo; Gene; Placenta; DNA methylation; Gene expression; Fetus","score_opus":0.011299033730312774,"score_gpt":0.3085661714741187,"score_spread":0.2972671377438059,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1483213138","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":[0.00011546097,0.99537873,0.0003949264,0.0004211582,0.00077094283,0.0000050301205,0.000020881726,0.0000132464365,0.002879692],"genre_scores_gemma":[0.0007299965,0.994356,0.00043056693,0.0003612971,0.0005756147,0.000008287574,0.00004200998,0.0000038490107,0.003492392],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.9998833,0.000015485908,0.000013913459,0.000023972307,0.000050298477,0.000012948132],"domain_scores_gemma":[0.99991465,0.0000338546,0.0000101805645,0.0000041853814,0.000024985846,0.000012136401],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.000389341,0.00068486936,0.0011878138,0.0012622921,0.0003025488,0.0010652097,0.0010176023,0.0011784862,0.0042788587],"category_scores_gemma":[0.00028614962,0.0003279718,0.0002976697,0.0016042092,0.000674053,0.0013458116,0.0007537384,0.0018129532,0.00302284],"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":[0.000110395864,0.00006335687,0.00017769805,0.007987697,0.000061220584,0.00045148484,0.00008629189,0.00041840784,0.009385725,0.017610405,0.08368848,0.8799588],"study_design_scores_gemma":[0.000007834906,0.000017847093,0.00023473402,0.000633112,0.000019061268,0.00060831953,0.00003385262,0.0000326875,0.00079437706,0.0023916373,0.9952194,0.0000071793406],"about_ca_topic_score_codex":0.0008586895,"about_ca_topic_score_gemma":0.0014890096,"teacher_disagreement_score":0.0042788587,"about_ca_system_score_codex":0.0008057626,"about_ca_system_score_gemma":0.00090956764,"threshold_uncertainty_score":0.014314234},"labels":[],"label_agreement":null},{"id":"W1488234983","doi":"10.1080/15592294.2015.1057383","title":"Beckwith–Wiedemann syndrome prenatal diagnosis by methylation analysis in chorionic villi","year":2015,"lang":"en","type":"article","venue":"Epigenetics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","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":"Pediatric Oncology Group","funders":"","keywords":"Beckwith–Wiedemann syndrome; Genomic imprinting; Methylation; DNA methylation; Biology; Chorionic villi; Imprinting (psychology); Differentially methylated regions; Genetics; Fetus; Internal medicine; Andrology; Prenatal diagnosis; Pregnancy; Gene; Medicine; Gene expression","score_opus":0.014964852298395202,"score_gpt":0.2582650396297488,"score_spread":0.24330018733135358,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1488234983","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99519724,0.0011687395,0.0024371322,0.00005318784,0.000010626788,0.000020987294,0.0002172935,0.00004771548,0.0008470476],"genre_scores_gemma":[0.99638295,0.00068983267,0.0024779646,0.00002550877,0.0000058634764,0.000012805275,0.00017284468,0.000010163811,0.00022209132],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9997305,0.000041971027,0.000023805831,0.000091645794,0.000072883915,0.000039024082],"domain_scores_gemma":[0.99985075,0.0000545054,0.000027999373,0.000016047681,0.00001929921,0.000031296924],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00018267256,0.00034765824,0.00020707972,0.0012134197,0.00017901722,0.00022079784,0.00014909545,0.00029475024,0.00052126625],"category_scores_gemma":[0.0007740186,0.0002172853,0.00018337811,0.0003287967,0.00025921408,0.00009698603,0.00029320506,0.0002961756,0.00011001831],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00048717659,0.000024446987,0.26853567,0.00009470135,0.00009900113,0.023793085,0.0008719594,0.00032413955,0.68091637,0.00025265868,0.00021430854,0.02438642],"study_design_scores_gemma":[0.000021958622,0.0002729551,0.73028296,0.00006194544,0.00013669344,0.084667996,0.00043640984,0.002319762,0.17803411,0.00043424976,0.0032961837,0.00003474036],"about_ca_topic_score_codex":0.0025665227,"about_ca_topic_score_gemma":0.0020432828,"teacher_disagreement_score":0.0025665227,"about_ca_system_score_codex":0.00018708057,"about_ca_system_score_gemma":0.00013140992,"threshold_uncertainty_score":0.005103171},"labels":[],"label_agreement":null},{"id":"W1491300853","doi":"10.1111/j.1758-8111.2012.00032.x","title":"Autonomic nervous system dysfunction in obesity and Prader–Willi syndrome: current evidence and implications for future obesity therapies","year":2011,"lang":"en","type":"article","venue":"Clinical Obesity","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":22,"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":"","keywords":"Medicine; Obesity; Autonomic nervous system; Childhood obesity; Bioinformatics; Endocrinology; Internal medicine; Heart rate; Blood pressure; Biology","score_opus":0.06107436963152304,"score_gpt":0.3204256370358156,"score_spread":0.2593512674042926,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1491300853","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":[0.0061446545,0.98309094,0.0011178536,0.006085869,0.0003895812,0.000016939395,0.000033746404,0.000027434793,0.0030929574],"genre_scores_gemma":[0.028807854,0.96588176,0.0020772868,0.0012171122,0.0011043035,0.000054746255,0.00006320057,0.0000051157003,0.0007886533],"study_design_codex":"design_other","study_design_gemma":"observational","domain_scores_codex":[0.999848,0.000050374467,0.00002403127,0.00002281236,0.000038144426,0.000016530508],"domain_scores_gemma":[0.99957377,0.0002497072,0.000071973176,0.000015208709,0.000045410532,0.00004391671],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.000834217,0.00064123666,0.0012943032,0.0005765164,0.0002575623,0.00074443006,0.00073711906,0.0011664128,0.0031674448],"category_scores_gemma":[0.0008847354,0.00014497721,0.00045130763,0.00048048224,0.00075303344,0.00081753626,0.00053510634,0.0016726722,0.00058236386],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0015059302,0.0007881883,0.006794764,0.007987642,0.00042586963,0.0037240346,0.00013115624,0.0005009192,0.010701175,0.009540268,0.0073219,0.95057815],"study_design_scores_gemma":[0.0026726644,0.008353119,0.11399568,0.026236808,0.0041650943,0.04252019,0.0018659324,0.0031504133,0.013490132,0.075949855,0.7073038,0.00029634],"about_ca_topic_score_codex":0.000271515,"about_ca_topic_score_gemma":0.0005570082,"teacher_disagreement_score":0.0031674448,"about_ca_system_score_codex":0.00031434564,"about_ca_system_score_gemma":0.00082694093,"threshold_uncertainty_score":0.010596156},"labels":[],"label_agreement":null},{"id":"W1493379081","doi":"10.1111/cge.12143","title":"Beckwith–Wiedemann and Silver–Russell syndromes: opposite developmental imbalances in imprinted regulators of placental function and embryonic growth","year":2013,"lang":"en","type":"review","venue":"Clinical Genetics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","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":"Child and Family Research Institute; University of British Columbia","funders":"Canadian Institutes of Health Research; Canada Research Chairs","keywords":"Beckwith–Wiedemann syndrome; Genomic imprinting; Epigenetics; Biology; Imprinting (psychology); Phenotype; Embryonic stem cell; Genetics; Function (biology); Gene; Loss function; Endocrinology; DNA methylation; Gene expression","score_opus":0.04321345216059616,"score_gpt":0.3246826767803114,"score_spread":0.28146922461971524,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1493379081","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":[0.0002997702,0.99760747,0.00020854594,0.00028042137,0.0001246977,0.0000037653792,0.000025351372,0.0000145186095,0.0014353925],"genre_scores_gemma":[0.0014461951,0.9973515,0.00032543286,0.0001653978,0.00009131904,0.000004697961,0.000052039315,0.000002167945,0.0005611538],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.9998541,0.00001951824,0.000029336501,0.000023727285,0.000055898967,0.000017394088],"domain_scores_gemma":[0.9998442,0.000061422215,0.00003161898,0.0000040426157,0.00003540729,0.000023315242],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0003316417,0.00076181605,0.0010004552,0.0024492189,0.000211419,0.00062034396,0.00064577756,0.0007325271,0.0025010041],"category_scores_gemma":[0.0005347864,0.00019595139,0.00034213962,0.0018915713,0.00041008336,0.00078215613,0.0005687539,0.0010045044,0.0014967325],"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":[0.0000674058,0.000027584962,0.00058817194,0.007940905,0.00009532904,0.0015466599,0.00005216705,0.00017469398,0.0019014255,0.0027863265,0.02071664,0.96410275],"study_design_scores_gemma":[0.000023885965,0.000061135994,0.0020914814,0.0024685906,0.00018223989,0.021755436,0.00011168728,0.00006169099,0.0008612649,0.0019020376,0.9704542,0.000026347001],"about_ca_topic_score_codex":0.001128086,"about_ca_topic_score_gemma":0.002375008,"teacher_disagreement_score":0.0025010041,"about_ca_system_score_codex":0.00046849705,"about_ca_system_score_gemma":0.0008960168,"threshold_uncertainty_score":0.008366704},"labels":[],"label_agreement":null},{"id":"W1494956959","doi":"10.1186/1471-2156-2-22","title":"A necdin/MAGE-like gene in the chromosome 15 autism susceptibility region: expression, imprinting, and mapping of the human and mouse orthologues","year":2001,"lang":"en","type":"article","venue":"BMC Genetics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":33,"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":"Medical Research Council; Canadian Institutes of Health Research; RIKEN; Alberta Heritage Foundation for Medical Research; Fondation pour la Recherche Médicale; University of Alberta; Eunice Kennedy Shriver National Institute of Child Health and Human Development; University of Miami; March of Dimes Foundation","keywords":"Genomic imprinting; Angelman syndrome; Genetics; Biology; Imprinting (psychology); Gene; Chromosome 15; Synteny; Allele; UBE3A; Gene cluster; Uniparental disomy; Chromosome 7 (human); Chromosome; Autism; Human genome; Neurodevelopmental disorder; Genome; Gene expression; DNA methylation; Karyotype; Medicine","score_opus":0.025309143560509898,"score_gpt":0.25171348208316513,"score_spread":0.22640433852265524,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1494956959","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.996003,0.0010006303,0.0018322273,0.00004746851,0.00000485647,0.000008852056,0.00023001133,0.00004416137,0.0008287411],"genre_scores_gemma":[0.9938545,0.00042459703,0.0029835866,0.000031571206,0.0000036100814,0.000014292999,0.0007760471,0.000007558246,0.0019042554],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9999379,0.0000069361454,0.0000035839241,0.000028607032,0.000014778593,0.0000081852095],"domain_scores_gemma":[0.99995685,0.0000067033566,0.000015296038,0.0000050247777,0.000002991583,0.000013134126],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0000814153,0.00017260728,0.00010330564,0.0002561241,0.00010149347,0.00013453799,0.00013338985,0.00022166607,0.0011908493],"category_scores_gemma":[0.0001047993,0.000095655145,0.000114136856,0.0001261293,0.00014679952,0.000089548,0.00022517961,0.0001352177,0.0002884403],"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":[0.00017844298,0.000010418025,0.0030249723,0.000045369172,0.000012664445,0.0005408031,0.000035275938,0.00010942832,0.9909361,0.00022952228,0.00005785102,0.0048191375],"study_design_scores_gemma":[0.0001546106,0.0008652815,0.42150995,0.00006738386,0.00015955514,0.029135466,0.000152006,0.0028904867,0.5228947,0.00086086727,0.021287112,0.00002258857],"about_ca_topic_score_codex":0.00058066065,"about_ca_topic_score_gemma":0.0008450139,"teacher_disagreement_score":0.0011908493,"about_ca_system_score_codex":0.00023593169,"about_ca_system_score_gemma":0.00013591653,"threshold_uncertainty_score":0.003983736},"labels":[],"label_agreement":null},{"id":"W1508174106","doi":"10.1111/j.1399-0004.2005.00420.x","title":"Inherited microdeletions that give rise to Beckwith–Wiedemann syndrome","year":2005,"lang":"en","type":"article","venue":"Clinical Genetics","topic":"Genetic Syndromes and Imprinting","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":"Spinal Cord Injury BC; Pacific Centre for Reproductive Medicine","funders":"","keywords":"Citation; Associate editor; Medicine; Library science; Computer science","score_opus":0.046803420956331145,"score_gpt":0.3402945591288867,"score_spread":0.2934911381725555,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1508174106","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.98406255,0.0025925762,0.0028396486,0.00073370273,0.00019653047,0.000028706452,0.00040104333,0.00022657502,0.008918719],"genre_scores_gemma":[0.9963916,0.00085241196,0.0017180041,0.00013528287,0.00007696829,0.000008039969,0.00011685012,0.000031066225,0.0006696502],"study_design_codex":"case_report","study_design_gemma":"observational","domain_scores_codex":[0.9997466,0.000035239147,0.000029389996,0.000050811585,0.000071161616,0.00006671812],"domain_scores_gemma":[0.9995034,0.00017228247,0.00014418714,0.000020792284,0.000025878093,0.0001335408],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00014578622,0.0014840008,0.0004448856,0.0016158298,0.00049029366,0.00053429627,0.00028300725,0.0011749867,0.0027176747],"category_scores_gemma":[0.0017070262,0.0004996522,0.0003115441,0.001028132,0.0008505941,0.00037804892,0.0008270394,0.0005866208,0.00047063548],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00046670742,0.000072304116,0.055153582,0.000091248556,0.00013661632,0.85561985,0.0005039464,0.00059185346,0.0647827,0.0036796783,0.0021112605,0.016790368],"study_design_scores_gemma":[0.00003911333,0.00010262827,0.05442692,0.000041030504,0.00017227732,0.92535144,0.00021573082,0.0004564013,0.015101955,0.0012976795,0.0027508643,0.000043941043],"about_ca_topic_score_codex":0.0010781033,"about_ca_topic_score_gemma":0.0011708528,"teacher_disagreement_score":0.0027176747,"about_ca_system_score_codex":0.00021138048,"about_ca_system_score_gemma":0.00039494684,"threshold_uncertainty_score":0.0090914965},"labels":[],"label_agreement":null},{"id":"W1508259436","doi":"10.1111/j.1399-0004.2006.00595b.x","title":"The beat goes on: ciliary proteins are defective in Meckel syndrome.","year":2006,"lang":"en","type":"article","venue":"Clinical Genetics","topic":"Genetic Syndromes and Imprinting","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":"Pacific Centre for Reproductive Medicine","funders":"","keywords":"Citation; Library science; Medicine; Computer science","score_opus":0.02120420260376018,"score_gpt":0.3003213630940957,"score_spread":0.2791171604903355,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1508259436","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9729222,0.01221397,0.0014106102,0.0042412067,0.00044022882,0.0000347051,0.0003284666,0.00026053883,0.008148196],"genre_scores_gemma":[0.995398,0.0016359198,0.00058400625,0.00048874796,0.00012912227,0.0000059477125,0.000071500326,0.000034511486,0.0016523757],"study_design_codex":"case_report","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99977165,0.000026894371,0.000021184092,0.000040059353,0.00009237595,0.000047764683],"domain_scores_gemma":[0.99953115,0.00017150302,0.00012527998,0.00001824487,0.000037577185,0.000116334944],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00018690637,0.0008435578,0.00038752987,0.0011125135,0.0005422762,0.00043305338,0.0004931051,0.001989809,0.0018807101],"category_scores_gemma":[0.0013444071,0.0002186972,0.00014124507,0.0007054416,0.001448841,0.00042335739,0.0006266515,0.00083963556,0.0003054546],"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":[0.0018190922,0.00009507589,0.057341743,0.0004767556,0.00013428836,0.67879945,0.0009440788,0.00050134864,0.19768257,0.006498018,0.009374263,0.0463334],"study_design_scores_gemma":[0.00013908876,0.00043266168,0.114758134,0.00017773562,0.00024652603,0.79916394,0.0007037774,0.00095674477,0.065560155,0.004846353,0.012934045,0.00008087946],"about_ca_topic_score_codex":0.0019824451,"about_ca_topic_score_gemma":0.001986733,"teacher_disagreement_score":0.001989809,"about_ca_system_score_codex":0.00039692372,"about_ca_system_score_gemma":0.00037704545,"threshold_uncertainty_score":0.0062915683},"labels":[],"label_agreement":null},{"id":"W1509596159","doi":"10.1002/0471719188.ch11","title":"Genomic Imprinting: An Epigenetic Modification","year":2005,"lang":"en","type":"other","venue":"","topic":"Genetic Syndromes and Imprinting","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":"University of Waterloo","funders":"","keywords":"Genomic imprinting; Imprinting (psychology); Epigenetics; Computational biology; Genetics; Biology; DNA methylation; Gene; Gene expression","score_opus":0.014443267439466466,"score_gpt":0.26154370902221824,"score_spread":0.24710044158275177,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1509596159","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":[0.0067905397,0.43286318,0.015703555,0.008514605,0.00675373,0.0000701091,0.00088628917,0.0006757818,0.5277422],"genre_scores_gemma":[0.032572526,0.43515915,0.0070279227,0.003149465,0.0031312592,0.000058181762,0.0007661967,0.00013705058,0.51799834],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.9999063,0.0000129507025,0.0000064817796,0.000018351062,0.0000456678,0.000010282514],"domain_scores_gemma":[0.9999552,0.00001401537,0.0000066061825,0.000007218444,0.000008961842,0.000008140371],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00022419011,0.00039541116,0.00041735935,0.0005995698,0.00025257366,0.0013546486,0.0005094614,0.00068734266,0.032865528],"category_scores_gemma":[0.00020941813,0.00014569244,0.00019507558,0.00086226675,0.00053761987,0.0011082392,0.0006690663,0.00069593376,0.007845975],"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":[0.00009264577,0.00003689787,0.00033389154,0.0012432379,0.000023585422,0.00095719984,0.00018670304,0.0004334165,0.026127916,0.09148692,0.08804963,0.79102796],"study_design_scores_gemma":[0.000004120374,0.000013162669,0.00043075343,0.00009853792,0.0000069939288,0.0006615435,0.000052983116,0.000043867112,0.0064271716,0.0055314475,0.9867242,0.0000053358735],"about_ca_topic_score_codex":0.0005683169,"about_ca_topic_score_gemma":0.0009993094,"teacher_disagreement_score":0.032865528,"about_ca_system_score_codex":0.0004943793,"about_ca_system_score_gemma":0.00042728957,"threshold_uncertainty_score":0.10994613},"labels":[],"label_agreement":null},{"id":"W1511421526","doi":"10.25011/cim.v31i4.4814","title":"INVESTIGATING THE MOLECULAR AND DEVELOPMENTAL EFFECTS OF VARIOUS CULTURE REGIMES IN A MOUSE MODEL SYSTEM","year":2008,"lang":"en","type":"article","venue":"Clinical and investigative medicine","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":0,"is_retracted":false,"has_abstract":true,"route_ca_aff":false,"route_ca_fund":false,"route_ca_venue":true,"route_about_ca":false,"ca_institutions":"","funders":"","keywords":"Genomic imprinting; Imprinting (psychology); Epigenetics; DNA methylation; Biology; Embryonic stem cell; Genetics; Methylation; Blastocyst; Embryo; Embryogenesis; Gene; Gene expression","score_opus":0.04804502277395591,"score_gpt":0.28375778637825905,"score_spread":0.23571276360430313,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1511421526","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.976689,0.006019341,0.012519137,0.00024265346,0.00014924488,0.00020371887,0.0017086616,0.00025313045,0.0022150336],"genre_scores_gemma":[0.9472305,0.0067587644,0.030440962,0.00038288996,0.00009652958,0.00084113097,0.0031228806,0.00021383348,0.010912447],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.999418,0.00009354039,0.000059472233,0.00014862552,0.00020028857,0.00008012356],"domain_scores_gemma":[0.9993851,0.00013235342,0.00018613011,0.00010686861,0.00010359671,0.0000858982],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0007580106,0.0007383853,0.00041431,0.0010868552,0.00041435342,0.00051281456,0.0006288823,0.0005942009,0.0015173503],"category_scores_gemma":[0.00035447776,0.00027412828,0.0007340022,0.00036712657,0.00048221013,0.000547799,0.00037301355,0.0014763394,0.0005364348],"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":[0.0001793966,0.00013262827,0.00067537546,0.000058758327,0.000014475583,0.000057066598,0.000033498196,0.00008453367,0.99693596,0.000053795062,0.000058755017,0.0017157048],"study_design_scores_gemma":[0.000013644411,0.0011555207,0.005117609,0.000012846374,0.000073119656,0.00015328942,0.00004433566,0.000505552,0.9916148,0.00003232493,0.0012669327,0.000010026907],"about_ca_topic_score_codex":0.0013789507,"about_ca_topic_score_gemma":0.0028658435,"teacher_disagreement_score":0.0015173503,"about_ca_system_score_codex":0.00063789793,"about_ca_system_score_gemma":0.0003586279,"threshold_uncertainty_score":0.0050760508},"labels":[],"label_agreement":null},{"id":"W1523114210","doi":"10.14740/jmc.v6i6.2108","title":"13q Deletion in a Girl Contributing to Antenatal Stroke, Insulin Resistance and Lymphedema Praecox: Expanding the Clinical Spectrum","year":2015,"lang":"en","type":"article","venue":"Journal of Medical Cases","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":0,"is_retracted":false,"has_abstract":true,"route_ca_aff":false,"route_ca_fund":false,"route_ca_venue":true,"route_about_ca":false,"ca_institutions":"","funders":"","keywords":"Medicine; Lymphedema; Phenotype; Pediatrics; Internal medicine; Genetics; Biology; Gene; Cancer","score_opus":0.034914787226028234,"score_gpt":0.34096686581080904,"score_spread":0.3060520785847808,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1523114210","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9954555,0.000605803,0.0007280025,0.00057891716,0.000024936058,0.00004207649,0.00012975855,0.000043812714,0.0023912126],"genre_scores_gemma":[0.9975103,0.00080904766,0.0005960897,0.00011955529,0.000048776277,0.000014633791,0.00007097773,0.0000110205,0.0008195875],"study_design_codex":"case_report","study_design_gemma":"case_report","domain_scores_codex":[0.9997923,0.000023183773,0.000020893283,0.000064335894,0.000033243123,0.00006607031],"domain_scores_gemma":[0.9996871,0.00009456274,0.00007942428,0.000012332171,0.00001879727,0.00010780655],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00013667825,0.00092529715,0.0005122357,0.0013496752,0.0007330435,0.0005164829,0.0003990417,0.0010868567,0.0018399853],"category_scores_gemma":[0.0010248808,0.0006059486,0.00027144665,0.0008936887,0.000842939,0.0005512139,0.00079049135,0.0009935333,0.00044115222],"study_design_candidate":"case_report","study_design_consensus":"case_report","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00003853065,0.000028788523,0.019155491,0.00001555114,0.000003840985,0.9753794,0.00020853979,0.000049554514,0.0032627645,0.00014192834,0.0001263028,0.0015893682],"study_design_scores_gemma":[0.000009898181,0.000061630504,0.016923105,0.0000089297855,0.000007551339,0.9817901,0.00010579377,0.00010248038,0.0005282165,0.0001144366,0.00034118223,0.000006698019],"about_ca_topic_score_codex":0.0014803475,"about_ca_topic_score_gemma":0.0014829597,"teacher_disagreement_score":0.0018399853,"about_ca_system_score_codex":0.00034907134,"about_ca_system_score_gemma":0.00044418746,"threshold_uncertainty_score":0.0061553717},"labels":[],"label_agreement":null},{"id":"W1524830710","doi":"10.1111/j.1365-2052.2007.01576.x","title":"<i>IGF2</i> gene characterization and association with rib eye area in beef cattle","year":2007,"lang":"en","type":"article","venue":"Animal Genetics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","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":"University of Saskatchewan","funders":"Natural Sciences and Engineering Research Council of Canada; University of Saskatchewan","keywords":"Biology; Exon; SNP; Intron; Genetics; Single-nucleotide polymorphism; Allele; Insulin-like growth factor 2; Gene; Beef cattle; Pseudogene; Molecular biology; Genotype; Gene expression; Genome","score_opus":0.007008328429296687,"score_gpt":0.22174429415542435,"score_spread":0.21473596572612766,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1524830710","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9995409,0.00007561359,0.0001406168,0.000014060023,0.0000024040723,0.0000011771214,0.00008815063,0.00000276175,0.00013431793],"genre_scores_gemma":[0.9991391,0.000056100725,0.00024124584,0.000030875373,0.000007914637,0.0000035603841,0.0002325896,0.000006177578,0.00028247244],"study_design_codex":"observational","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99977773,0.000047948717,0.000013690767,0.00007056028,0.000051783063,0.000038326172],"domain_scores_gemma":[0.9997062,0.000077453195,0.000091340444,0.000012905013,0.00003545636,0.00007662278],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00027614555,0.00023124149,0.00020049234,0.00086294365,0.0002889809,0.00027458108,0.00021657317,0.0002666202,0.00090666075],"category_scores_gemma":[0.00034159777,0.000121294346,0.0001884579,0.00051836896,0.0003146671,0.00006314839,0.000110142704,0.00027453422,0.00013964207],"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":[0.0017428336,0.00013255497,0.6628967,0.00006664819,0.00020214207,0.0027716674,0.0006304689,0.0003430794,0.32030597,0.00019646953,0.0002826939,0.010428772],"study_design_scores_gemma":[0.000016194226,0.0001707007,0.9913019,0.0000095037485,0.00004348862,0.002775337,0.00010736512,0.0006019878,0.0044269976,0.000046432717,0.00049271894,0.000007420397],"about_ca_topic_score_codex":0.005385842,"about_ca_topic_score_gemma":0.0043369243,"teacher_disagreement_score":0.005385842,"about_ca_system_score_codex":0.00022222304,"about_ca_system_score_gemma":0.00011359722,"threshold_uncertainty_score":0.010708988},"labels":[],"label_agreement":null},{"id":"W1527923796","doi":"10.1002/ajmg.c.31363","title":"Molecular Findings in Beckwith–Wiedemann Syndrome","year":2013,"lang":"en","type":"review","venue":"American Journal of Medical Genetics Part C Seminars in Medical Genetics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":218,"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":"Canadian Institutes of Health Research","keywords":"Beckwith–Wiedemann syndrome; Genomic imprinting; Phenotype; Biology; Gene; Genetics; Imprinting (psychology); Chromosome; Chromosomal region; Gene cluster; Computational biology; Gene expression; DNA methylation","score_opus":0.017444303452404154,"score_gpt":0.32568973281826974,"score_spread":0.3082454293658656,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1527923796","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":[0.00034712892,0.9976713,0.00012591494,0.00027619896,0.00016088571,0.0000026092493,0.000018531673,0.0000107664455,0.0013866439],"genre_scores_gemma":[0.002156822,0.996754,0.00019588548,0.00018706503,0.00016555192,0.0000033607605,0.000036393438,0.0000015529234,0.00049943937],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.99989593,0.00001652074,0.000016384609,0.000020631987,0.000038058282,0.000012496962],"domain_scores_gemma":[0.9999126,0.000037252987,0.000016658343,0.0000030692327,0.000018095121,0.000012186713],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00027451827,0.0005751366,0.0008470115,0.0021485249,0.00017206171,0.0005926947,0.00063069025,0.0009658575,0.002189347],"category_scores_gemma":[0.00043701436,0.0002009942,0.0002473989,0.0014479383,0.00046853838,0.0005203846,0.0004852067,0.0009953884,0.0013363048],"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":[0.00008193878,0.000033769073,0.00069778797,0.007644963,0.00008793908,0.005182937,0.00009740163,0.00033028412,0.0046726842,0.00599122,0.036518183,0.9386609],"study_design_scores_gemma":[0.000024238512,0.000045893776,0.0025325187,0.0028161863,0.00014573985,0.03463148,0.00009002599,0.00008387025,0.0014754325,0.0028256343,0.9552998,0.00002914144],"about_ca_topic_score_codex":0.00094525825,"about_ca_topic_score_gemma":0.0012201808,"teacher_disagreement_score":0.002189347,"about_ca_system_score_codex":0.0005592904,"about_ca_system_score_gemma":0.0006200109,"threshold_uncertainty_score":0.00732404},"labels":[],"label_agreement":null},{"id":"W1530079397","doi":"10.1159/000106818","title":"Possible Non-Mendelian Mechanisms of Thyroid Dysgenesis","year":2007,"lang":"en","type":"review","venue":"Endocrine development","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":65,"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; Université de Montréal","funders":"Endocrine Fellows Foundation","keywords":"Thyroid; Dysgenesis; Mendelian inheritance; Agenesis; Hypoplasia; Ectopic thyroid; PAX8; Medicine; Biology; Bioinformatics; Pathology; Genetics; Internal medicine; Gene; Transcription factor","score_opus":0.02826277671095831,"score_gpt":0.31069866190791323,"score_spread":0.28243588519695495,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1530079397","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":[0.00025715973,0.99728835,0.00029650435,0.0002523176,0.0001291206,0.0000032475405,0.000010299541,0.000017616785,0.0017453522],"genre_scores_gemma":[0.0014553856,0.99711573,0.00028664622,0.00016612548,0.00012426676,0.0000062543227,0.000024813353,0.0000020892812,0.0008186881],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.9997415,0.000045641944,0.000034668494,0.00005721824,0.00009588486,0.00002505943],"domain_scores_gemma":[0.99974793,0.00015009909,0.000030561034,0.000010136004,0.00004302823,0.000018320601],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0006065507,0.0008174252,0.0016298364,0.0020247803,0.00032545137,0.00087112666,0.0010556334,0.0011670057,0.0031428493],"category_scores_gemma":[0.00072405254,0.00025426524,0.0004089138,0.0014358726,0.0007991212,0.001071,0.000503534,0.0011277776,0.0018534043],"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":[0.00006438254,0.000048592923,0.0006599779,0.008957822,0.00010496142,0.002835133,0.000108295935,0.00047958817,0.0025227729,0.008063413,0.018176174,0.95797884],"study_design_scores_gemma":[0.000034116267,0.000075961856,0.0024406367,0.0028037825,0.00011747902,0.020496255,0.00016920819,0.00012589268,0.0011973642,0.0068671093,0.96563864,0.000033544577],"about_ca_topic_score_codex":0.0011567797,"about_ca_topic_score_gemma":0.0014195275,"teacher_disagreement_score":0.0031428493,"about_ca_system_score_codex":0.000798165,"about_ca_system_score_gemma":0.0011480739,"threshold_uncertainty_score":0.010513902},"labels":[],"label_agreement":null},{"id":"W1530807287","doi":"10.1155/2015/474097","title":"PWS/AS MS-MLPA Confirms Maternal Origin of 15q11.2 Microduplication","year":2015,"lang":"en","type":"article","venue":"Case Reports in Genetics","topic":"Genetic Syndromes and Imprinting","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":"University of Manitoba; Shared Health; Winnipeg Regional Health Authority","funders":"","keywords":"Multiplex ligation-dependent probe amplification; Angelman syndrome; Genetics; Gene duplication; Genomic imprinting; Copy-number variation; Imprinting (psychology); Chromosome 15; Uniparental disomy; Biology; Medicine; Gene; Chromosome; DNA methylation; Genome; Karyotype","score_opus":0.023169774058054888,"score_gpt":0.2889852929844233,"score_spread":0.26581551892636845,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1530807287","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9912985,0.0006685723,0.0055114687,0.00018056025,0.000028977138,0.000018711615,0.00028431808,0.00015771126,0.0018513312],"genre_scores_gemma":[0.996938,0.00025112275,0.0016651879,0.000042895183,0.00001270549,0.0000067757765,0.00017502761,0.000012054247,0.0008963503],"study_design_codex":"bench_or_experimental","study_design_gemma":"case_report","domain_scores_codex":[0.9997857,0.000019028741,0.000018710212,0.00007881487,0.000049989252,0.000047853628],"domain_scores_gemma":[0.9998462,0.000046333553,0.000028454277,0.000013982604,0.000025065689,0.00003997201],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00014581306,0.0003159802,0.00020513908,0.0009569511,0.00016629056,0.00015429642,0.00018257486,0.0003177668,0.0019755918],"category_scores_gemma":[0.00041796174,0.00014285241,0.00017556468,0.00018271175,0.00028405339,0.000120822,0.00026048627,0.00038820188,0.00041212555],"study_design_candidate":"case_report","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00018384821,0.000029166042,0.04457896,0.000062480554,0.000020962983,0.031887095,0.0002808759,0.00010966976,0.9150905,0.00021635629,0.00026378097,0.007276398],"study_design_scores_gemma":[0.000025985337,0.00063817424,0.29255596,0.000021092028,0.000092597526,0.15409403,0.0002839254,0.0032629273,0.5425131,0.00031140665,0.0061775944,0.000023140929],"about_ca_topic_score_codex":0.0016065914,"about_ca_topic_score_gemma":0.0021341282,"teacher_disagreement_score":0.0019755918,"about_ca_system_score_codex":0.00018092594,"about_ca_system_score_gemma":0.000120890094,"threshold_uncertainty_score":0.0066090226},"labels":[],"label_agreement":null},{"id":"W1533681919","doi":"10.1023/a:1009489624045","title":"Toward a More Meaningful In Vitro Fertilization Success Rate","year":2000,"lang":"en","type":"article","venue":"Journal of Assisted Reproduction and Genetics","topic":"Genetic Syndromes and Imprinting","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":"London Health Sciences Centre; Western University","funders":"","keywords":"Reproductive medicine; In vitro fertilisation; Human fertilization; Biology; Andrology; Medicine; Gynecology; Pregnancy; Genetics","score_opus":0.018220350293160843,"score_gpt":0.2636646057124651,"score_spread":0.24544425541930423,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1533681919","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":[0.29449856,0.015425478,0.6342107,0.007382963,0.0011479378,0.00038266543,0.0023921041,0.0019869707,0.042572565],"genre_scores_gemma":[0.78809637,0.005100945,0.19234522,0.0022577138,0.00045622146,0.000585087,0.0017017708,0.000562827,0.008893864],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9911389,0.004635604,0.00087422604,0.0010674138,0.0020889016,0.00019491836],"domain_scores_gemma":[0.98418415,0.008981914,0.001315241,0.0019509,0.0031718458,0.0003959438],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.015247033,0.0006773669,0.0017063137,0.0014858348,0.0004948935,0.00276441,0.0016140783,0.002062188,0.0028234317],"category_scores_gemma":[0.024074314,0.00038099126,0.00057894806,0.0010017854,0.00072458026,0.0022276456,0.0014677122,0.002558109,0.002648239],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.001102305,0.0008651472,0.03989916,0.0009993925,0.00026541617,0.0002676533,0.0005543932,0.017206438,0.62072736,0.04450401,0.004964606,0.26864403],"study_design_scores_gemma":[0.00008443556,0.0032972817,0.053550538,0.00029272866,0.00038884275,0.0021478983,0.00029430405,0.039174452,0.836214,0.025214547,0.039134495,0.00020643052],"about_ca_topic_score_codex":0.00038514918,"about_ca_topic_score_gemma":0.00032340348,"teacher_disagreement_score":0.015247033,"about_ca_system_score_codex":0.0010072719,"about_ca_system_score_gemma":0.0005842808,"threshold_uncertainty_score":0.08063495},"labels":[],"label_agreement":null},{"id":"W1541412888","doi":"10.1038/npg.els.0001451","title":"Chromosomal Genetic Disease: Numerical Aberrations","year":2001,"lang":"en","type":"other","venue":"Encyclopedia of Life Sciences","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","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":"University of British Columbia","funders":"","keywords":"Meiosis; Biology; Mitosis; Genetics; Disease; Gene; Medicine; Pathology","score_opus":0.010357884867660077,"score_gpt":0.2539945433579645,"score_spread":0.24363665849030444,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1541412888","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":[0.040211618,0.15732518,0.011372912,0.007481134,0.002728757,0.000271294,0.024418985,0.0017797123,0.75441045],"genre_scores_gemma":[0.2979338,0.14011264,0.008884403,0.0031895991,0.0018124977,0.0001427204,0.01849312,0.00032200583,0.5291092],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.99986076,0.000024945335,0.000015608755,0.000029515033,0.00004892843,0.000020310532],"domain_scores_gemma":[0.999703,0.00008743328,0.000060791193,0.00003132302,0.0000650398,0.000052318544],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00016158092,0.00076568406,0.00051624817,0.0016379054,0.0002951667,0.0009358694,0.0003670356,0.00061885646,0.06555497],"category_scores_gemma":[0.00080591085,0.000062155494,0.00014709643,0.0022125705,0.00029369214,0.0003706925,0.00048478067,0.0004861298,0.020635676],"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":[0.00050536654,0.00015912988,0.012104745,0.0021211875,0.00007235228,0.021317825,0.00014514122,0.00043650574,0.017420461,0.011770568,0.3442474,0.58969945],"study_design_scores_gemma":[0.000048799844,0.000061818995,0.020423684,0.00078976137,0.000072331655,0.09485924,0.00010387803,0.00018219743,0.004183946,0.005460776,0.8737888,0.000024763032],"about_ca_topic_score_codex":0.000941438,"about_ca_topic_score_gemma":0.0010430878,"teacher_disagreement_score":0.06555497,"about_ca_system_score_codex":0.00024749865,"about_ca_system_score_gemma":0.00020915155,"threshold_uncertainty_score":0.21930325},"labels":[],"label_agreement":null},{"id":"W1542745269","doi":"10.1002/mrd.22220","title":"Epigenetic regulation of genomic imprinting from germ line to preimplantation","year":2013,"lang":"en","type":"review","venue":"Molecular Reproduction and Development","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":61,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Children’s Health Research Institute; Western University","funders":"Natural Sciences and Engineering Research Council of Canada; Children's Health Research Institute","keywords":"Biology; Epigenetics; Genomic imprinting; Reprogramming; DNA methylation; Genetics; Imprinting (psychology); Epigenome; Gene; Gene expression","score_opus":0.029224737161846006,"score_gpt":0.28547310980945634,"score_spread":0.25624837264761036,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1542745269","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":[0.00020565563,0.99724674,0.00034873825,0.00021157824,0.00017791563,0.000004051216,0.000026190926,0.000019722718,0.0017593629],"genre_scores_gemma":[0.0010888561,0.9976368,0.00024416318,0.00010871752,0.000105704166,0.00000549743,0.000029654415,0.000002155754,0.0007784884],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.99986875,0.000017691698,0.000017149083,0.0000313005,0.00004930576,0.000015674395],"domain_scores_gemma":[0.99985003,0.00005520126,0.00002939124,0.0000067197675,0.000038301394,0.000020299587],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0002727081,0.0006742949,0.0009069766,0.0017047054,0.0002433651,0.0006428148,0.0008106182,0.0006924213,0.0025090433],"category_scores_gemma":[0.00039623378,0.00020960653,0.0002843772,0.0020137518,0.000588886,0.0008390705,0.0005726358,0.0011256459,0.0021871605],"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":[0.000058413734,0.000036411315,0.00031344112,0.010502939,0.00005836635,0.00034307112,0.0000709112,0.0004154854,0.006097126,0.0055966973,0.019779403,0.95672774],"study_design_scores_gemma":[0.0000075521602,0.00004244513,0.0017857758,0.0013712939,0.00005496874,0.0015876007,0.00004990029,0.00008290768,0.002090424,0.002693565,0.99021345,0.000020066816],"about_ca_topic_score_codex":0.0008794445,"about_ca_topic_score_gemma":0.0013013205,"teacher_disagreement_score":0.0025090433,"about_ca_system_score_codex":0.00074378226,"about_ca_system_score_gemma":0.0006932083,"threshold_uncertainty_score":0.008393645},"labels":[],"label_agreement":null},{"id":"W1547804365","doi":"10.1071/rdv16n1ab26","title":"26 ABERRANT REPROGRAMMING OF IMPRINTED GENE EXPRESSION IN ENLARGED PLACENTAS OF MICE CLONED FROM ES CELLS TREATED WITH TSA OR 5AZAC","year":2004,"lang":"en","type":"article","venue":"Reproduction Fertility and Development","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":0,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Cegep de Saint Hyacinthe; Université de Montréal; University of Guelph","funders":"International Council for Canadian Studies; Natural Sciences and Engineering Research Council of Canada; Türkiye Bilimsel ve Teknolojik Araştırma Kurumu; Ontario Ministry of Agriculture, Food and Rural Affairs","keywords":"Genomic imprinting; Biology; DNA methylation; Reprogramming; Epigenetics; Molecular biology; XIST; Gene; Gene expression; Somatic cell nuclear transfer; Histone; Housekeeping gene; Andrology; Genetics; X-inactivation; Blastocyst; X chromosome; Embryogenesis","score_opus":0.01444423078156517,"score_gpt":0.23031228009727714,"score_spread":0.21586804931571196,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1547804365","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99362034,0.0008736506,0.0033865098,0.00006207891,0.000033601154,0.000021466665,0.00053490134,0.0000811407,0.0013863201],"genre_scores_gemma":[0.99004185,0.0009470149,0.0025411246,0.00006421604,0.000012764496,0.000055059776,0.0011281637,0.000072139665,0.0051376526],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9997482,0.00003522361,0.000025163003,0.00007061083,0.00007746479,0.000043416116],"domain_scores_gemma":[0.9997732,0.000050843282,0.000064943895,0.000033106196,0.000019478934,0.0000584151],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00018687127,0.00031796165,0.00031348193,0.0003810027,0.00009754048,0.00030630207,0.00024245813,0.00021699979,0.0019748304],"category_scores_gemma":[0.0001494225,0.0002123558,0.0003327825,0.00015822788,0.0003287312,0.00015691157,0.0002477369,0.00059533556,0.00041047783],"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":[0.000024688381,0.000003331368,0.00007029645,0.0000076732795,0.0000022602794,0.00003436126,0.0000112684,0.000009566031,0.99960226,0.000019082543,0.000004129685,0.00021110277],"study_design_scores_gemma":[0.000008567757,0.00018045175,0.008284498,0.00000521331,0.000017719716,0.00022654756,0.00004426811,0.0003613118,0.98948294,0.000030455856,0.0013548773,0.0000030313302],"about_ca_topic_score_codex":0.0006452685,"about_ca_topic_score_gemma":0.00052507536,"teacher_disagreement_score":0.0019748304,"about_ca_system_score_codex":0.0002185736,"about_ca_system_score_gemma":0.00016440634,"threshold_uncertainty_score":0.0066064596},"labels":[],"label_agreement":null},{"id":"W1569183880","doi":"10.1034/j.1399-0004.2000.570505.x","title":"Somatic segregation errors predominantly contribute to the gain or loss of a paternal chromosome leading to uniparental disomy for chromosome 15","year":2000,"lang":"en","type":"article","venue":"Clinical Genetics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":105,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Children’s Health Research Institute; BC Research (Canada); University of British Columbia; Children's & Women's Health Centre of British Columbia","funders":"Medical Research Council","keywords":"Uniparental disomy; Biology; Genetics; Meiosis II; Meiosis; Chromosome; Trisomy; Chromosome 21; Nondisjunction; Aneuploidy; Angelman syndrome; Chromosome 15; Karyotype; Gene","score_opus":0.03454083384588958,"score_gpt":0.3398858196890891,"score_spread":0.3053449858431995,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1569183880","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9939956,0.0017405538,0.0018795201,0.000048110043,0.000022823051,0.000016615322,0.00014452482,0.00006086228,0.002091446],"genre_scores_gemma":[0.99784064,0.00070201955,0.0002942779,0.000023229653,0.00001604982,0.0000048264997,0.00015033198,0.000012271978,0.00095629063],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9996276,0.000050522445,0.000047070193,0.00010495745,0.000104932034,0.00006480279],"domain_scores_gemma":[0.99927694,0.00014889748,0.00036257546,0.000068421905,0.0000609018,0.00008227935],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00021279785,0.00039169085,0.00040511857,0.0005878743,0.00017495173,0.0003626867,0.00023726103,0.00025296502,0.003843756],"category_scores_gemma":[0.0010306058,0.00017352594,0.00024264106,0.00038038718,0.00033618434,0.00022863002,0.00030719815,0.0001610538,0.000820645],"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":[0.0010669084,0.00013403225,0.62542355,0.0004391271,0.00029102384,0.013200909,0.00043935582,0.00040222655,0.28168976,0.0014798655,0.00069721934,0.07473596],"study_design_scores_gemma":[0.00005418485,0.0006941827,0.8579755,0.000060625374,0.00022928618,0.06563611,0.00027940993,0.0006584953,0.06482917,0.00061987323,0.008942261,0.0000209646],"about_ca_topic_score_codex":0.00036253995,"about_ca_topic_score_gemma":0.0003887196,"teacher_disagreement_score":0.003843756,"about_ca_system_score_codex":0.00017139087,"about_ca_system_score_gemma":0.00018882788,"threshold_uncertainty_score":0.012858629},"labels":[],"label_agreement":null},{"id":"W1580157617","doi":"10.1046/j.1432-1327.2000.01438.x","title":"<i>H19</i> sense and antisense transgenes modify insulin‐like growth factor‐II mRNA levels","year":2000,"lang":"en","type":"article","venue":"European Journal of Biochemistry","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":50,"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; Université de Montréal; Centre Hospitalier Universitaire Sainte-Justine","funders":"","keywords":"Sense (electronics); Transgene; Messenger RNA; Insulin-like growth factor; Antisense RNA; Biology; Cell biology; Growth factor; Molecular biology; Genetics; Chemistry; Gene; Receptor","score_opus":0.012952441494805346,"score_gpt":0.216362423715647,"score_spread":0.20340998222084167,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1580157617","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9899593,0.00041461544,0.0054985983,0.00011875997,0.000093798626,0.000027823051,0.000889229,0.00015318462,0.0028448042],"genre_scores_gemma":[0.9856287,0.00061574415,0.005528609,0.00011173844,0.000037020196,0.00005545763,0.0020179993,0.00011635359,0.0058882637],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9999194,0.000008373737,0.0000067702804,0.000027974871,0.00001609719,0.000021376767],"domain_scores_gemma":[0.9998903,0.000026967995,0.000029956938,0.000010970701,0.000011519838,0.000030203326],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.000092100716,0.00031788496,0.00012834663,0.00011156518,0.00009341821,0.00022771825,0.00015538368,0.00013323376,0.0019053963],"category_scores_gemma":[0.00007942844,0.00012335775,0.00018556621,0.000082308725,0.00022044173,0.0001277152,0.00010287987,0.00042176823,0.00043882837],"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":[0.000031667532,0.0000060465404,0.00006339716,0.0000054303855,0.0000014582491,0.000008113597,0.0000028307365,0.0000061514847,0.9996314,0.00003535259,0.00001751187,0.00019057085],"study_design_scores_gemma":[0.000008377302,0.00009955843,0.0021637718,0.0000015275563,0.0000071517634,0.000054066397,0.00001171174,0.00021860733,0.99614954,0.000017501106,0.0012667166,0.0000014736011],"about_ca_topic_score_codex":0.0007422302,"about_ca_topic_score_gemma":0.0010905993,"teacher_disagreement_score":0.0019053963,"about_ca_system_score_codex":0.00025583585,"about_ca_system_score_gemma":0.00013797502,"threshold_uncertainty_score":0.0063741207},"labels":[],"label_agreement":null},{"id":"W1580837527","doi":"10.1108/978-1-60752-633-9","title":"A Recipe for Success","year":2007,"lang":"en","type":"book","venue":"","topic":"Genetic Syndromes and Imprinting","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":"University of Calgary","funders":"","keywords":"Recipe; Computer science; History; Ancient history","score_opus":0.0152232298869932,"score_gpt":0.27150528701785326,"score_spread":0.25628205713086005,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1580837527","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":[0.0025275694,0.016943417,0.0046350816,0.072091356,0.02225058,0.0003042889,0.0006057671,0.0016463859,0.8789955],"genre_scores_gemma":[0.011560679,0.0063070576,0.004685514,0.026052168,0.0022725163,0.00021398212,0.00045668808,0.0009095406,0.94754183],"study_design_codex":"not_applicable","study_design_gemma":"not_applicable","domain_scores_codex":[0.9974554,0.00067894,0.000072692616,0.00030616438,0.0010855246,0.00040132867],"domain_scores_gemma":[0.9981932,0.00029202385,0.00008309609,0.00023762617,0.0005057894,0.0006882413],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0017033913,0.001742409,0.0009819252,0.001706334,0.009286192,0.012606334,0.002155014,0.004494497,0.20280294],"category_scores_gemma":[0.0051699504,0.0005027314,0.0009886548,0.0010407978,0.004117507,0.011267715,0.011112462,0.009279676,0.14088471],"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":[0.000026081823,0.00006812151,0.00014460202,0.00020512223,0.0000075361118,0.00019606191,0.002367893,0.00004013049,0.0002083119,0.0372629,0.88560694,0.073866196],"study_design_scores_gemma":[0.0000024133055,0.000009306265,0.00007061752,0.000100311656,0.0000013650308,0.00007575417,0.000981335,0.000012129963,0.000019785848,0.0019992045,0.9967229,0.000005035549],"about_ca_topic_score_codex":0.0042608213,"about_ca_topic_score_gemma":0.010266014,"teacher_disagreement_score":0.20280294,"about_ca_system_score_codex":0.002262812,"about_ca_system_score_gemma":0.0032168573,"threshold_uncertainty_score":0.67844343},"labels":[],"label_agreement":null},{"id":"W1581926946","doi":"10.1038/npg.els.0002013","title":"Autosomal Recessive Traits and Diseases","year":2006,"lang":"en","type":"other","venue":"Encyclopedia of Life Sciences","topic":"Genetic Syndromes and Imprinting","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; Hospital for Sick Children; University of Toronto","funders":"","keywords":"Loss of heterozygosity; Consanguinity; Genetics; Biology; Phenotype; Mutant; Gene; Evolutionary biology; Allele","score_opus":0.007398009793705506,"score_gpt":0.24103135174946375,"score_spread":0.23363334195575824,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1581926946","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":[0.046709906,0.24082658,0.03360145,0.008754837,0.0041229012,0.0004763328,0.03494283,0.003722499,0.6268427],"genre_scores_gemma":[0.29257295,0.16744784,0.031077258,0.0061347582,0.0026175852,0.0005506577,0.027284577,0.00069921796,0.4716152],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.9992416,0.00017014683,0.000080238635,0.00014912327,0.00024637228,0.000112518974],"domain_scores_gemma":[0.9993175,0.00018910109,0.00020044326,0.00007529881,0.00012778111,0.00008978177],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00053845806,0.0014389724,0.00096628285,0.0016254414,0.0007078474,0.0014258376,0.0006771755,0.0009002506,0.0348807],"category_scores_gemma":[0.0014835091,0.00013668177,0.00040954503,0.0024640886,0.00085759663,0.00059230364,0.00096927397,0.0009335953,0.015968695],"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":[0.0005116421,0.00012639495,0.014481193,0.0024774442,0.00025075965,0.014732057,0.0003956791,0.0004988283,0.026102541,0.09161628,0.28624004,0.5625671],"study_design_scores_gemma":[0.000050246144,0.00004836338,0.011061419,0.0007397318,0.00009122981,0.033503454,0.00011860273,0.00013856149,0.0036966526,0.014363857,0.936155,0.000032891345],"about_ca_topic_score_codex":0.0010158559,"about_ca_topic_score_gemma":0.0011410231,"teacher_disagreement_score":0.0348807,"about_ca_system_score_codex":0.0005250348,"about_ca_system_score_gemma":0.0005588623,"threshold_uncertainty_score":0.116687536},"labels":[],"label_agreement":null},{"id":"W1589590998","doi":"10.1038/ejhg.2009.106","title":"Beckwith–Wiedemann syndrome","year":2009,"lang":"en","type":"review","venue":"European Journal of Human Genetics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":690,"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; Hospital for Sick Children","funders":"","keywords":"Beckwith–Wiedemann syndrome; Epigenetics; Genomic imprinting; Imprinting (psychology); Monozygotic twin; Epigenesis; Genetics; Biology; Genetic disorder; Carcinogenesis; Medicine; DNA methylation; Cancer; Gene","score_opus":0.03914682175189165,"score_gpt":0.3037019688950376,"score_spread":0.26455514714314593,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1589590998","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":[0.0013072499,0.9916174,0.001159345,0.00061061856,0.00062293274,0.0000051602765,0.00003311731,0.000038783357,0.0046053748],"genre_scores_gemma":[0.013793304,0.98035276,0.0016682913,0.0005759687,0.0006292529,0.000011937843,0.000107673746,0.000007970997,0.002852789],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.9998901,0.00001593804,0.000017558248,0.000021076366,0.000038469716,0.000016823813],"domain_scores_gemma":[0.99989855,0.000050208473,0.000016579717,0.0000057767747,0.000011868511,0.000016954986],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00021774718,0.00086995785,0.0009828368,0.0017345911,0.00021505397,0.0004403235,0.0007454001,0.0009702048,0.002068975],"category_scores_gemma":[0.00040056717,0.00018718852,0.00023370447,0.0016552228,0.0005401995,0.00052440085,0.00065185287,0.0008976446,0.0009928826],"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":[0.00009830514,0.00003994058,0.0007189521,0.0021833486,0.00010328891,0.01243993,0.000039699702,0.00030046707,0.0026175834,0.0037956308,0.0233853,0.95427763],"study_design_scores_gemma":[0.000054957996,0.00004275539,0.0027964122,0.0017146913,0.0002374927,0.10052191,0.00010143821,0.00015594308,0.0024427883,0.0028961035,0.8890008,0.000034639597],"about_ca_topic_score_codex":0.00063399615,"about_ca_topic_score_gemma":0.0014371161,"teacher_disagreement_score":0.002068975,"about_ca_system_score_codex":0.0003929948,"about_ca_system_score_gemma":0.00059334416,"threshold_uncertainty_score":0.0069214106},"labels":[],"label_agreement":null},{"id":"W1611812925","doi":"","title":"Fetal-placental calcium metabolism in mice partly or fully deficient in parathyroid hormone","year":2010,"lang":"en","type":"dissertation","venue":"Memorial University Research Repository (Memorial University)","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":0,"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":"Canadian Institutes of Health Research; American Society for Bone and Mineral Research","keywords":"Internal medicine; Endocrinology; Parathyroid hormone; Fetus; Calcium metabolism; Placenta; Homeostasis; Calcium; Biology; Medicine; Pregnancy","score_opus":0.020281668304955307,"score_gpt":0.26809375791952195,"score_spread":0.24781208961456663,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1611812925","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9848392,0.003468543,0.006161981,0.0005703854,0.000118791424,0.000085902466,0.0021594116,0.00036020135,0.0022356582],"genre_scores_gemma":[0.9742294,0.004235234,0.007231632,0.0002974519,0.00006874158,0.00029383844,0.0022032766,0.00029295037,0.011147587],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99933404,0.00008542768,0.00009353172,0.00021115343,0.00016027912,0.000115637224],"domain_scores_gemma":[0.9991812,0.00013244977,0.00034147213,0.00009838553,0.000038586273,0.00020789122],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0004651421,0.0008569873,0.00071012403,0.0019118567,0.0004785196,0.0007978103,0.0007789651,0.001062613,0.0028206727],"category_scores_gemma":[0.00039965022,0.0008126903,0.00071914843,0.00050486886,0.0012152571,0.0006892364,0.0006407822,0.0017198437,0.0007814465],"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":[0.0011536594,0.0001357517,0.00038238763,0.000088832145,0.0000179817,0.0007261069,0.00010809185,0.00012103785,0.99488914,0.0006386375,0.00007125383,0.0016671395],"study_design_scores_gemma":[0.00063945015,0.0025775665,0.0115681235,0.0000973836,0.00021869535,0.0066040345,0.0003654486,0.002093725,0.9635725,0.0012366209,0.010968829,0.0000576454],"about_ca_topic_score_codex":0.0013071334,"about_ca_topic_score_gemma":0.0013167892,"teacher_disagreement_score":0.0028206727,"about_ca_system_score_codex":0.0006455428,"about_ca_system_score_gemma":0.00063681847,"threshold_uncertainty_score":0.009436071},"labels":[],"label_agreement":null},{"id":"W1633153776","doi":"10.1523/jneurosci.0777-15.2015","title":"<i>Zac1</i>Regulates the Differentiation and Migration of Neocortical Neurons via<i>Pac1</i>","year":2015,"lang":"en","type":"article","venue":"Journal of Neuroscience","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":37,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Alberta Children's Hospital; University of Calgary","funders":"Alberta Children's Hospital Research Institute; Agence Nationale de la Recherche; Canadian Institutes of Health Research; March of Dimes Foundation","keywords":"Biology; Gene knockdown; Transcription factor; Neuropeptide; Cell biology; Gene; Genetics; Receptor","score_opus":0.017933263176699594,"score_gpt":0.24574910639225991,"score_spread":0.2278158432155603,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1633153776","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9817603,0.0047562732,0.00590572,0.0003443713,0.000056772034,0.000039416493,0.0016411499,0.00037385453,0.0051221345],"genre_scores_gemma":[0.98645705,0.0031608867,0.0035319184,0.0001622886,0.000016845252,0.000083359635,0.0011631214,0.00009480549,0.005329665],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9999058,0.000007260734,0.0000074711666,0.000026898495,0.000025650255,0.000026891033],"domain_scores_gemma":[0.99992955,0.0000053420345,0.00003379565,0.000005430601,0.000008803436,0.000016957016],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.000070000286,0.00036079602,0.00018580277,0.00024462666,0.0002430386,0.0004804941,0.0002314815,0.00023222849,0.0010192877],"category_scores_gemma":[0.00008544658,0.00019428687,0.00017203891,0.00016293033,0.0003086934,0.0001715246,0.00021781279,0.00063136977,0.0004153142],"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":[0.000059163147,0.0000053351487,0.00027761533,0.00003204764,0.0000032577395,0.000028429078,0.000008472018,0.000093562165,0.99781823,0.00023242616,0.00008740862,0.0013541554],"study_design_scores_gemma":[0.000020230811,0.000057769896,0.015122541,0.000010679062,0.000023003133,0.00014150515,0.00003091256,0.0019831604,0.97579044,0.000106785075,0.00670452,0.0000084682],"about_ca_topic_score_codex":0.0028541146,"about_ca_topic_score_gemma":0.0050049718,"teacher_disagreement_score":0.0028541146,"about_ca_system_score_codex":0.00058490236,"about_ca_system_score_gemma":0.0003650643,"threshold_uncertainty_score":0.005675018},"labels":[],"label_agreement":null},{"id":"W16865929","doi":"10.1007/978-0-387-70765-5_15","title":"Respiratory control abnormalities in necdinnull mice: implications for the pathogenesis of Prader-Willi syndrome","year":2007,"lang":"en","type":"book-chapter","venue":"","topic":"Genetic Syndromes and Imprinting","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 Alberta","funders":"","keywords":"Pathogenesis; Respiratory system; Medicine; Pediatrics; Pathology; Internal medicine","score_opus":0.03275829016341943,"score_gpt":0.2724878892491701,"score_spread":0.23972959908575067,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W16865929","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.69346076,0.11627905,0.061849296,0.007925447,0.0011926799,0.000060359554,0.0020434745,0.0024258494,0.1147631],"genre_scores_gemma":[0.80329007,0.06470713,0.025731564,0.00089934823,0.00015645954,0.000078569785,0.0008984241,0.0002507777,0.103987604],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9999416,0.0000069866,0.00000467274,0.000012246929,0.00002725493,0.000007284409],"domain_scores_gemma":[0.9999354,0.000025633015,0.0000137184925,0.000006359864,0.0000057281727,0.000013132667],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0001154242,0.0003474248,0.00030119758,0.0002808162,0.00013477051,0.00038474004,0.0006200094,0.000661888,0.0023112372],"category_scores_gemma":[0.00011312914,0.00019662948,0.00013732923,0.0001846361,0.00046190893,0.00036847618,0.000309251,0.00089123973,0.0007430394],"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":[0.00010643856,0.000015268466,0.00039872935,0.0001160561,0.000009643174,0.0022982177,0.00008973486,0.00041370824,0.9519897,0.011209676,0.0020635473,0.031289242],"study_design_scores_gemma":[0.00006987244,0.00028746415,0.01791299,0.00015156445,0.00009975651,0.037806116,0.00021434497,0.0030515743,0.75704557,0.019484567,0.16379254,0.00008360236],"about_ca_topic_score_codex":0.0002935578,"about_ca_topic_score_gemma":0.0005150204,"teacher_disagreement_score":0.0023112372,"about_ca_system_score_codex":0.00026606966,"about_ca_system_score_gemma":0.00013772685,"threshold_uncertainty_score":0.007731855},"labels":[],"label_agreement":null},{"id":"W1710646799","doi":"10.1002/047001153x.g103106","title":"Imprinting and epigenetic inheritance in human disease","year":2005,"lang":"en","type":"other","venue":"Encyclopedia of Genetics, Genomics, Proteomics and Bioinformatics","topic":"Genetic Syndromes and Imprinting","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":"McGill University Health Centre","funders":"","keywords":"Imprinting (psychology); Genomic imprinting; Epigenetics; Genetics; Biology; Phenotype; Inheritance (genetic algorithm); Gene silencing; Gene; Disease; DNA methylation; Gene expression; Medicine","score_opus":0.005710718871114667,"score_gpt":0.22088864432457747,"score_spread":0.21517792545346281,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1710646799","genre_codex":"review","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":[0.0046859775,0.89128304,0.0039932416,0.003906717,0.0012225641,0.000020385476,0.0007524188,0.00023193021,0.09390374],"genre_scores_gemma":[0.045730352,0.8608638,0.0043226546,0.0019943425,0.0012371765,0.000032456028,0.0007553622,0.000042395684,0.0850215],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.9999163,0.000021268215,0.0000066826724,0.000014664793,0.00003132334,0.000009719402],"domain_scores_gemma":[0.9999044,0.000040867893,0.000015279258,0.000007320539,0.000018515604,0.000013650897],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00019796721,0.00032233968,0.00036325696,0.0008847071,0.0001970155,0.0008442694,0.00029677962,0.0005984945,0.019862905],"category_scores_gemma":[0.00035257053,0.00006676508,0.0001280867,0.0013292568,0.00032252935,0.0004655189,0.00059208856,0.00053463527,0.0042613414],"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":[0.00010269504,0.000039034036,0.0017640346,0.0022331867,0.000037467453,0.0013443773,0.00020001677,0.0007610923,0.0073776008,0.040407088,0.111025855,0.83470756],"study_design_scores_gemma":[0.0000080268355,0.00003268314,0.004280624,0.000776468,0.000024493485,0.004228226,0.000096949116,0.00017425795,0.00172693,0.01815377,0.97048396,0.000013628088],"about_ca_topic_score_codex":0.00087025505,"about_ca_topic_score_gemma":0.0013522092,"teacher_disagreement_score":0.019862905,"about_ca_system_score_codex":0.00040491126,"about_ca_system_score_gemma":0.0003043773,"threshold_uncertainty_score":0.06644809},"labels":[],"label_agreement":null},{"id":"W1721320528","doi":"10.1071/rdv16n1ab35","title":"35 ANALYSIS OF EPIGENETIC MODIFICATIONS AND GENOMIC IMPRINTING IN NUCLEAR TRANSFER DERIVED BOS GAURUS × B. TAURUS CONCEPTI","year":2004,"lang":"en","type":"article","venue":"Reproduction Fertility and Development","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":0,"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 Guelph","funders":"International Council for Canadian Studies; Natural Sciences and Engineering Research Council of Canada; Türkiye Bilimsel ve Teknolojik Araştırma Kurumu; Ontario Ministry of Agriculture, Food and Rural Affairs","keywords":"XIST; Genomic imprinting; Biology; Imprinting (psychology); Epigenetics; Somatic cell nuclear transfer; X-inactivation; Genetics; Locus (genetics); Reprogramming; DNA methylation; X chromosome; Molecular biology; Embryo; Gene; Blastocyst; Embryogenesis; Gene expression","score_opus":0.018384983305854505,"score_gpt":0.23603074126735674,"score_spread":0.21764575796150223,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1721320528","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9952982,0.0010923858,0.0013684318,0.000023891229,0.000012887651,0.00003082507,0.0003086274,0.00002848141,0.0018362582],"genre_scores_gemma":[0.99244267,0.00081675226,0.001344591,0.000034558656,0.000008404323,0.000051359093,0.0011200396,0.000023747853,0.0041578],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99988556,0.000015134974,0.000007406953,0.000033197026,0.00003771986,0.000021092479],"domain_scores_gemma":[0.99987113,0.000033031225,0.000031967546,0.000012427257,0.000011426003,0.00004000035],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00018460845,0.00025774186,0.0001773906,0.00057159894,0.000246374,0.00023470129,0.00021067787,0.00028328397,0.00129205],"category_scores_gemma":[0.00014277262,0.00014534804,0.00020888925,0.00014992415,0.00025622154,0.00012216714,0.00024129213,0.000405185,0.00027153725],"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":[0.000050591934,0.000010553323,0.0007513121,0.0000130092885,0.000003923449,0.00018676747,0.00005247275,0.000013913101,0.99801123,0.00004816608,0.000006997601,0.000851058],"study_design_scores_gemma":[0.000029017463,0.001357156,0.17604415,0.000028195722,0.000074827716,0.00424423,0.00042284795,0.00084730244,0.80966574,0.000104329,0.007155114,0.000027063763],"about_ca_topic_score_codex":0.0030821227,"about_ca_topic_score_gemma":0.003153372,"teacher_disagreement_score":0.0030821227,"about_ca_system_score_codex":0.00033483928,"about_ca_system_score_gemma":0.00016517597,"threshold_uncertainty_score":0.0061283708},"labels":[],"label_agreement":null},{"id":"W1724866995","doi":"10.1007/978-0-387-77576-0_6","title":"Genomic Imprinting and Human Psychology: Cognition, Behavior and Pathology","year":2008,"lang":"en","type":"article","venue":"Advances in experimental medicine and biology","topic":"Genetic Syndromes and Imprinting","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":"SickKids Foundation; University of Toronto","funders":"","keywords":"Genomic imprinting; Imprinting (psychology); Cognition; Psychology; Neuropathology; Angelman syndrome; Autism; Neuroscience; Developmental psychology; Biology; Genetics; Gene; Disease; DNA methylation; Medicine","score_opus":0.027430392531922598,"score_gpt":0.3617527594039637,"score_spread":0.3343223668720411,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1724866995","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":[0.24815728,0.6116685,0.035252813,0.039746933,0.0014394588,0.000043838212,0.00038477412,0.00039213343,0.062914275],"genre_scores_gemma":[0.86746645,0.11542958,0.008024596,0.002118665,0.00095699436,0.00004029056,0.00010385609,0.0000364894,0.0058231493],"study_design_codex":"design_other","study_design_gemma":"theoretical_or_conceptual","domain_scores_codex":[0.9997528,0.0001069581,0.000008610301,0.00003956027,0.00007307388,0.000019063351],"domain_scores_gemma":[0.9991678,0.0005763782,0.00006142276,0.000059679525,0.000053201904,0.000081514074],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0007035982,0.00044551367,0.0005392992,0.0008007365,0.0003332432,0.002114703,0.0005139996,0.0010559824,0.0026673782],"category_scores_gemma":[0.0019860968,0.0001637783,0.00012401954,0.00093864306,0.005409442,0.0018451043,0.00048942165,0.0011690847,0.0002492192],"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":[0.00052345445,0.0004332118,0.038140178,0.0011738922,0.0002213635,0.0009009341,0.0033793638,0.0029449556,0.03347275,0.42932254,0.010106337,0.47938102],"study_design_scores_gemma":[0.000055146145,0.0002711028,0.14119464,0.00023849447,0.000087848064,0.0018964357,0.0026731852,0.0022070843,0.0047460496,0.7947744,0.051754583,0.00010104137],"about_ca_topic_score_codex":0.0023193238,"about_ca_topic_score_gemma":0.002267662,"teacher_disagreement_score":0.0026673782,"about_ca_system_score_codex":0.00090293604,"about_ca_system_score_gemma":0.0011692657,"threshold_uncertainty_score":0.008923233},"labels":[],"label_agreement":null},{"id":"W1725933063","doi":"10.1002/ajmg.a.35249","title":"Energy homeostasis in Prader–Willi Syndrome: How clinical research informs studies of animal models of genetic obesity","year":2012,"lang":"en","type":"letter","venue":"American Journal of Medical Genetics Part A","topic":"Genetic Syndromes and Imprinting","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 Alberta","funders":"","keywords":"Medical genetics; Gerontology; Library science; Medicine; Genetics; Biology; Gene","score_opus":0.09859789480529922,"score_gpt":0.3847313034169727,"score_spread":0.28613340861167347,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1725933063","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":[0.0006443335,0.0020164633,0.00022659687,0.9842794,0.01193756,0.000005160383,0.00001443732,0.000013568105,0.00086251367],"genre_scores_gemma":[0.018231746,0.005680198,0.00086520665,0.8152937,0.15561375,0.000040934043,0.000025014222,0.000028260509,0.0042210803],"study_design_codex":"not_applicable","study_design_gemma":"not_applicable","domain_scores_codex":[0.9974427,0.0011953665,0.00033876466,0.00024720535,0.0005567773,0.0002190778],"domain_scores_gemma":[0.98742515,0.009260682,0.00048704323,0.00037176465,0.0014350701,0.0010201648],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.005773736,0.00081280526,0.0016129898,0.0006626709,0.0021311743,0.0020596215,0.0011769331,0.033344526,0.0017759511],"category_scores_gemma":[0.02487935,0.00046562566,0.0007451142,0.0004621994,0.0039247004,0.003455178,0.0012595447,0.02553816,0.0014304667],"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":[0.00035198696,0.00012219591,0.0024082197,0.0001613109,0.000061937324,0.0113078775,0.0004130914,0.00017823878,0.00082305714,0.012285711,0.930643,0.041243218],"study_design_scores_gemma":[0.00075184467,0.00045407738,0.0063005085,0.0008017936,0.00018874073,0.024084117,0.000964994,0.002253703,0.001089962,0.08993678,0.87293446,0.00023897892],"about_ca_topic_score_codex":0.0024015491,"about_ca_topic_score_gemma":0.004598002,"teacher_disagreement_score":0.033344526,"about_ca_system_score_codex":0.003232987,"about_ca_system_score_gemma":0.0022667602,"threshold_uncertainty_score":0.030534804},"labels":[],"label_agreement":null},{"id":"W1774553629","doi":"10.1385/1-59259-983-4:273","title":"Phenotypic Analysis of the Mouse Placenta","year":2005,"lang":"en","type":"article","venue":"Humana Press eBooks","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":60,"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 Calgary","funders":"","keywords":"Phenotype; Placenta; Biology; Mutant; Identification (biology); Computational biology; Genetics; Gene; Bioinformatics; Pregnancy; Fetus","score_opus":0.02372172660308965,"score_gpt":0.25178871776819794,"score_spread":0.22806699116510828,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1774553629","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.7290461,0.023109645,0.14602487,0.002226516,0.00054802536,0.00069470814,0.01646454,0.0046123527,0.0772733],"genre_scores_gemma":[0.7930993,0.026587842,0.093857594,0.00088898354,0.00010911824,0.0009389824,0.011633575,0.0013736439,0.07151094],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9997471,0.000045065,0.000028402605,0.000060356742,0.00008421644,0.000034819815],"domain_scores_gemma":[0.9998072,0.000039476945,0.0000390797,0.00004078216,0.000024984236,0.000048515718],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0004063929,0.00047755401,0.00028249048,0.0015731488,0.00036478613,0.00057737425,0.0005009531,0.0005493868,0.004163857],"category_scores_gemma":[0.0002611801,0.00033901224,0.0004254354,0.00046216458,0.00045401527,0.00030463826,0.00060459704,0.001053631,0.0017074122],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.000051585015,0.000018216697,0.00019727598,0.000070330585,0.000007381946,0.00033982532,0.000043707667,0.00011173882,0.99203426,0.0018599017,0.00030657355,0.0049593383],"study_design_scores_gemma":[0.000033132088,0.00028930738,0.011104954,0.00009624932,0.000055035118,0.004567485,0.00009160774,0.0010374353,0.9105885,0.0015269276,0.07058123,0.000028205375],"about_ca_topic_score_codex":0.0005146153,"about_ca_topic_score_gemma":0.0007681663,"teacher_disagreement_score":0.004163857,"about_ca_system_score_codex":0.00036335533,"about_ca_system_score_gemma":0.00023301918,"threshold_uncertainty_score":0.013929486},"labels":[],"label_agreement":null},{"id":"W1792639881","doi":"10.1186/1471-2164-16-s1-s12","title":"Whole-exome analysis of foetal autopsy tissue reveals a frameshift mutation in OBSL1, consistent with a diagnosis of 3-M Syndrome","year":2015,"lang":"en","type":"article","venue":"BMC Genomics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":27,"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; Trillium Health Centre; Credit Valley Hospital; Hospital for Sick Children","funders":"Hospital for Sick Children; University of Toronto; Government of Ontario; Genome Canada; Ontario Genomics; Ontario Genomics Institute","keywords":"Frameshift mutation; Biology; Exome sequencing; Autopsy; Exome; Genetics; Mutation; Computational biology; Evolutionary biology; Pathology; Medicine; Gene","score_opus":0.022054261627680583,"score_gpt":0.2584966924874054,"score_spread":0.23644243085972483,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1792639881","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99542266,0.00066165946,0.0016217995,0.00031046092,0.000025365109,0.000020283574,0.00074239424,0.000047234455,0.0011481667],"genre_scores_gemma":[0.99729,0.000337874,0.0010814628,0.0001184206,0.000014157574,0.0000101834485,0.00050012936,0.000009174046,0.00063862983],"study_design_codex":"case_report","study_design_gemma":"case_report","domain_scores_codex":[0.9999212,0.000008026767,0.000008504428,0.000025967618,0.000023368839,0.00001294887],"domain_scores_gemma":[0.9998336,0.000076275275,0.000035196837,0.000012189725,0.000013081982,0.000029676634],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00014979283,0.00039416377,0.00017002132,0.00075824966,0.00031152033,0.00021105404,0.00026634402,0.00079990027,0.0018256536],"category_scores_gemma":[0.00050923123,0.0001158367,0.0002441539,0.00022510684,0.00028678105,0.0001113986,0.00027934086,0.00037379222,0.00029842954],"study_design_candidate":"case_report","study_design_consensus":"case_report","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0004750269,0.00009406192,0.1032753,0.00016799034,0.00011674254,0.49237224,0.0009910273,0.00042575612,0.3829882,0.00046484274,0.0012084789,0.017420312],"study_design_scores_gemma":[0.000034762346,0.0002810292,0.27391103,0.00007362502,0.00013070344,0.6365715,0.0004818364,0.0013973208,0.08077579,0.0005309623,0.0057836394,0.00002779781],"about_ca_topic_score_codex":0.0008184817,"about_ca_topic_score_gemma":0.001397651,"teacher_disagreement_score":0.0018256536,"about_ca_system_score_codex":0.00021184699,"about_ca_system_score_gemma":0.00014832476,"threshold_uncertainty_score":0.0061074495},"labels":[],"label_agreement":null},{"id":"W1803951751","doi":"10.3109/10409238.2015.1064350","title":"Epigenetic events regulating monoallelic gene expression","year":2015,"lang":"en","type":"review","venue":"Critical Reviews in Biochemistry and Molecular Biology","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":27,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Simon Fraser University","funders":"","keywords":"Biology; Epigenetics; Genomic imprinting; DNA methylation; Genetics; Epigenetics of physical exercise; Chromatin; Gene; Histone; Regulation of gene expression; Gene expression","score_opus":0.04445219793211987,"score_gpt":0.38385586590428317,"score_spread":0.3394036679721633,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1803951751","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":[0.27197295,0.65828204,0.037626695,0.0014110882,0.0005801951,0.000076866185,0.001612997,0.0006741912,0.027762955],"genre_scores_gemma":[0.7666637,0.20525062,0.008234494,0.00075225846,0.00027926266,0.00008173132,0.0014432938,0.00007497656,0.017219631],"study_design_codex":"bench_or_experimental","study_design_gemma":"not_applicable","domain_scores_codex":[0.99980086,0.000018574276,0.00001621224,0.000075005686,0.000060805673,0.000028565084],"domain_scores_gemma":[0.9998437,0.00004148034,0.000051992534,0.00001292921,0.000030951414,0.00001887718],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00019705045,0.00023594878,0.00032333753,0.00031853054,0.00023000945,0.0006153525,0.00046019116,0.0003627358,0.0015854056],"category_scores_gemma":[0.00022803612,0.00014424804,0.00025032228,0.0003238561,0.0004415624,0.00047024916,0.00041403656,0.0005983505,0.0005225542],"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":[0.00015950637,0.00003586743,0.005377424,0.0017653053,0.000097023796,0.0013288694,0.00043147625,0.00045329894,0.8439759,0.012933276,0.0015902763,0.13185191],"study_design_scores_gemma":[0.00002707802,0.00046022717,0.085259266,0.00049780787,0.00034933104,0.008071725,0.0005329736,0.001690016,0.55360574,0.011358038,0.33803782,0.00011004136],"about_ca_topic_score_codex":0.00042363672,"about_ca_topic_score_gemma":0.00071117847,"teacher_disagreement_score":0.0015854056,"about_ca_system_score_codex":0.00037102116,"about_ca_system_score_gemma":0.0002656066,"threshold_uncertainty_score":0.005303681},"labels":[],"label_agreement":null},{"id":"W1833365966","doi":"10.1210/jc.2015-2503","title":"Macronutrient Regulation of Ghrelin and Peptide YY in Pediatric Obesity and Prader-Willi Syndrome","year":2015,"lang":"en","type":"article","venue":"The Journal of Clinical Endocrinology & Metabolism","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":22,"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":"Institute of Nutrition, Metabolism and Diabetes; National Institute of Diabetes and Digestive and Kidney Diseases; American Diabetes Association; Canadian Institutes of Health Research; Children's Hospital Foundation; Children's Miracle Network Hospitals; Children's Health Research Institute; Women and Children's Health Research Institute; Foundation for Prader-Willi Research; National Institutes of Health; Stollery Children’s Hospital Foundation; National Center for Research Resources","keywords":"Ghrelin; Internal medicine; Endocrinology; Peptide YY; Postprandial; Medicine; Insulin; Body mass index; Obesity; Crossover study; Hormone; Neuropeptide; Neuropeptide Y receptor; Receptor","score_opus":0.03420403284976331,"score_gpt":0.3181829048476714,"score_spread":0.2839788719979081,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1833365966","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99917537,0.0005949495,0.00008114959,0.000022570646,0.0000034042862,0.000008966868,0.000035408684,0.0000019661823,0.00007615124],"genre_scores_gemma":[0.99839276,0.00084054004,0.0004917713,0.000040840838,0.000012624277,0.00003005768,0.00012156759,0.000002169391,0.00006775011],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9997253,0.00010374005,0.000026111638,0.000049324262,0.00006132109,0.000034104814],"domain_scores_gemma":[0.999587,0.000117682765,0.00018466645,0.000016848928,0.00001773482,0.00007602918],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0004874506,0.0005240913,0.0004917969,0.00031804747,0.0001578403,0.00021525664,0.00017550327,0.00022944434,0.00079836126],"category_scores_gemma":[0.00076906313,0.00020703589,0.0003501983,0.0002943666,0.0005163594,0.00022960872,0.0003763084,0.00039514966,0.000058728816],"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":[0.012703556,0.00082683907,0.91952944,0.0004320803,0.00047294574,0.0017091502,0.00030821486,0.00054953486,0.036644258,0.00017066736,0.00023112554,0.026422119],"study_design_scores_gemma":[0.0002264042,0.0031973664,0.99270153,0.000018107887,0.00010722703,0.0012996669,0.00011930447,0.00024862555,0.001776319,0.00005067269,0.00025013933,0.000004571153],"about_ca_topic_score_codex":0.0010704324,"about_ca_topic_score_gemma":0.0013176943,"teacher_disagreement_score":0.0010704324,"about_ca_system_score_codex":0.00024860457,"about_ca_system_score_gemma":0.00028595954,"threshold_uncertainty_score":0.0026708245},"labels":[],"label_agreement":null},{"id":"W1838511334","doi":"10.1684/j.1950-6945.2005.tb00126.x","title":"Atypical absences and recurrent absence status in an adult with Angelman syndrome due to the UBE3A mutation","year":2005,"lang":"en","type":"article","venue":"Epileptic Disorders","topic":"Genetic Syndromes and Imprinting","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":"Toronto Western Hospital; University of Toronto","funders":"","keywords":"Angelman syndrome; UBE3A; Epilepsy; Pediatrics; Status epilepticus; Mentally retarded; Medicine; Psychomotor retardation; Chromosome 15; Psychology; Psychiatry; Genetics; Chromosome; Biology; Developmental psychology; Pathology","score_opus":0.005778018916728868,"score_gpt":0.23643874636807274,"score_spread":0.2306607274513439,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1838511334","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99695206,0.0004077712,0.000489652,0.00032128458,0.000030889605,0.000016914086,0.0000858291,0.000048513008,0.0016470993],"genre_scores_gemma":[0.99885976,0.00021650331,0.00023158471,0.00008923508,0.000053184336,0.000002897311,0.000047063826,0.0000062050804,0.0004935329],"study_design_codex":"case_report","study_design_gemma":"case_report","domain_scores_codex":[0.9999312,0.000008056558,0.000008781038,0.00001482683,0.000013891666,0.000023069915],"domain_scores_gemma":[0.9996897,0.00006540923,0.00011468363,0.000011449473,0.000015250081,0.000103552804],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0001042852,0.00064076565,0.00033164205,0.0005632768,0.00037654364,0.00020273455,0.00016364109,0.00079540163,0.0010307895],"category_scores_gemma":[0.00081183575,0.00024584885,0.0002601103,0.00026952696,0.00040156793,0.00038959252,0.00026429052,0.00057858095,0.00026496896],"study_design_candidate":"case_report","study_design_consensus":"case_report","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0001625046,0.000054091717,0.03492198,0.000029203286,0.00001538764,0.9536914,0.0003975336,0.000094848314,0.0074745268,0.00018646351,0.00028789646,0.0026840211],"study_design_scores_gemma":[0.000022684291,0.00023580453,0.066331334,0.000008269165,0.000023939743,0.93109083,0.00010283496,0.00026880173,0.0011315682,0.00012521334,0.0006465044,0.000012161101],"about_ca_topic_score_codex":0.0011598594,"about_ca_topic_score_gemma":0.0020025403,"teacher_disagreement_score":0.0011598594,"about_ca_system_score_codex":0.0001922121,"about_ca_system_score_gemma":0.00020250349,"threshold_uncertainty_score":0.0034483671},"labels":[],"label_agreement":null},{"id":"W1844199574","doi":"10.1038/ejhg.2015.224","title":"Prenatal molecular testing for Beckwith–Wiedemann and Silver–Russell syndromes: a challenge for molecular analysis and genetic counseling","year":2015,"lang":"en","type":"review","venue":"European Journal of Human Genetics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":63,"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":"Ministero della Salute; Institut National de la Santé et de la Recherche Médicale; Instituto de Salud Carlos III; Bundesministerium für Bildung und Forschung; National Institute for Health and Care Research","keywords":"Beckwith–Wiedemann syndrome; Genetic counseling; Genetic testing; Genetics; Prenatal diagnosis; Molecular genetics; Medicine; Biology; Computational biology; Pregnancy; Gene; Fetus","score_opus":0.050556555618824904,"score_gpt":0.30741652546420895,"score_spread":0.25685996984538406,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1844199574","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":[0.00014780389,0.9976375,0.00050892093,0.00088886986,0.00022211895,0.0000021118672,0.000015932932,0.000012573746,0.00056413753],"genre_scores_gemma":[0.0015192603,0.995955,0.0009640374,0.00058751134,0.00047783178,0.0000040080827,0.000048831,0.0000048523666,0.00043874138],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.9996094,0.000091960355,0.000047095695,0.00006937799,0.00015144187,0.000030726173],"domain_scores_gemma":[0.9987134,0.0008816921,0.000078057405,0.000030272015,0.00022722663,0.00006927047],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0011770424,0.0007770253,0.00155052,0.0021011913,0.00021693794,0.00079324335,0.0012658577,0.0013646653,0.0017396758],"category_scores_gemma":[0.00221122,0.00026243692,0.00046124298,0.0011740369,0.0007576235,0.0010811182,0.0007285852,0.0025054358,0.0007843269],"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":[0.00006200782,0.000034408306,0.0007723002,0.003344095,0.00006882773,0.0010776443,0.000039245406,0.000248506,0.0012501238,0.0030672394,0.029917885,0.9601177],"study_design_scores_gemma":[0.000043087442,0.00007291529,0.0029453,0.0061300555,0.00032154468,0.013720549,0.00016925657,0.0002904986,0.001144602,0.006652193,0.96845776,0.000052124928],"about_ca_topic_score_codex":0.0014551032,"about_ca_topic_score_gemma":0.002258851,"teacher_disagreement_score":0.0021011913,"about_ca_system_score_codex":0.0005969737,"about_ca_system_score_gemma":0.0012564821,"threshold_uncertainty_score":0.0062248707},"labels":[],"label_agreement":null},{"id":"W1849159271","doi":"10.1139/o11-033","title":"CTCF function is modulated by neighboring DNA binding factors","year":2011,"lang":"en","type":"review","venue":"Biochemistry and Cell Biology","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":60,"is_retracted":false,"has_abstract":true,"route_ca_aff":false,"route_ca_fund":false,"route_ca_venue":true,"route_about_ca":false,"ca_institutions":"","funders":"","keywords":"CTCF; Enhancer; Biology; DNA; DNA methylation; Genetics; Repressor; Molecular biology; Gene; Transcription factor; Gene expression","score_opus":0.021969894719404845,"score_gpt":0.25034473504490296,"score_spread":0.2283748403254981,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1849159271","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":[0.9714912,0.0074821925,0.0099264365,0.00012193993,0.00012045127,0.000033073688,0.00052293803,0.00054006296,0.009761704],"genre_scores_gemma":[0.99500185,0.00055629737,0.0007461759,0.0000361948,0.000012784087,0.000015251687,0.00041435342,0.000069205096,0.0031478363],"study_design_codex":"bench_or_experimental","study_design_gemma":"not_applicable","domain_scores_codex":[0.99958724,0.000021156342,0.00001178185,0.00011872971,0.00014737759,0.00011369466],"domain_scores_gemma":[0.9997869,0.0000317599,0.000034924265,0.000019310348,0.000030385267,0.00009666433],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00012489072,0.00028120252,0.00037610403,0.00033671616,0.00034050515,0.0007061589,0.00041642442,0.0003450046,0.003510499],"category_scores_gemma":[0.00053012994,0.00018032074,0.00021674899,0.00024748547,0.00021372487,0.00026616355,0.00054229173,0.0005258996,0.0011949764],"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":[0.000078473146,0.000020056494,0.0008650168,0.00004212584,0.0000075690355,0.00011895171,0.00002324518,0.0001172659,0.99260217,0.0003740641,0.00023582357,0.005515276],"study_design_scores_gemma":[0.000044934743,0.00015081666,0.031547125,0.000025144142,0.00002477881,0.0008156392,0.000061015337,0.0050299033,0.9379723,0.00035537616,0.023941921,0.00003102522],"about_ca_topic_score_codex":0.0037222921,"about_ca_topic_score_gemma":0.004979063,"teacher_disagreement_score":0.0037222921,"about_ca_system_score_codex":0.00069455366,"about_ca_system_score_gemma":0.00024127834,"threshold_uncertainty_score":0.011743784},"labels":[],"label_agreement":null},{"id":"W1857882766","doi":"10.1111/biom.12380","title":"Optimum Study Design for Detecting Imprinting and Maternal Effects Based on Partial Likelihood","year":2015,"lang":"en","type":"article","venue":"Biometrics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","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":"McGill University","funders":"Natural Sciences and Engineering Research Council of Canada; National Science Foundation","keywords":"Imprinting (psychology); Statistics; Econometrics; Computer science; Mathematics; Biology; Genetics","score_opus":0.033288574217492164,"score_gpt":0.2804025703448232,"score_spread":0.24711399612733104,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1857882766","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":[0.008411703,0.00056933175,0.9885308,0.0003162583,0.000039783168,0.0014618129,0.00011275623,0.000095010226,0.00046255055],"genre_scores_gemma":[0.12996294,0.0007797366,0.8609456,0.00027483414,0.000104974126,0.007008341,0.00023073427,0.000050359595,0.0006424882],"study_design_codex":"theoretical_or_conceptual","study_design_gemma":"theoretical_or_conceptual","domain_scores_codex":[0.7796742,0.20136867,0.0046674716,0.00749248,0.005678658,0.0011185749],"domain_scores_gemma":[0.6329204,0.3383114,0.009006985,0.013224266,0.005037738,0.0014992119],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.15291734,0.002040509,0.0051202932,0.0035125948,0.0010374227,0.002476372,0.003136,0.0037666338,0.0047942796],"category_scores_gemma":[0.29273355,0.0019361741,0.003642654,0.0024295938,0.004080676,0.004214837,0.0038473948,0.0028675895,0.00063015154],"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":[0.008432649,0.0008248926,0.029519385,0.0053029964,0.00519766,0.0013183292,0.0016971813,0.1496947,0.008900061,0.4146083,0.002768099,0.37173584],"study_design_scores_gemma":[0.0031288904,0.008146403,0.011309057,0.00088760303,0.0030360087,0.00094651326,0.00029963243,0.51920706,0.005645385,0.43931746,0.007830261,0.00024567117],"about_ca_topic_score_codex":0.0006460044,"about_ca_topic_score_gemma":0.0006315687,"teacher_disagreement_score":0.15291734,"about_ca_system_score_codex":0.0018079095,"about_ca_system_score_gemma":0.0041915383,"threshold_uncertainty_score":0.80871385},"labels":[],"label_agreement":null},{"id":"W1909009273","doi":"10.1034/j.1399-0004.2001.590303.x","title":"The role of genomic imprinting in human developmental disorders: lessons from Prader–Willi syndrome","year":2001,"lang":"en","type":"review","venue":"Clinical Genetics","topic":"Genetic Syndromes and Imprinting","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 Alberta","funders":"","keywords":"Genomic imprinting; Angelman syndrome; Biology; Imprinting (psychology); Genetics; Gene; Human genome; Allele; Chromosome 15; Chromatin; Gene expression; DNA methylation; Chromosome; Genome","score_opus":0.059810896672741545,"score_gpt":0.3811113413316443,"score_spread":0.3213004446589028,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1909009273","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":[0.00015308536,0.9977506,0.0002624091,0.00068115327,0.00022330706,0.0000021900896,0.00000805287,0.00000969089,0.0009096597],"genre_scores_gemma":[0.00088278024,0.9976185,0.0003265672,0.00028494294,0.00024578001,0.0000035651274,0.00001405114,0.0000015121345,0.00062226667],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.99985003,0.00003246291,0.000021074598,0.000029594794,0.000054763113,0.0000120260975],"domain_scores_gemma":[0.9996966,0.00014026713,0.000026815012,0.000012533102,0.0000801433,0.00004371442],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0006093226,0.00072968233,0.0013250444,0.0013487327,0.00025371817,0.00069389207,0.0009341799,0.0010743482,0.0022386783],"category_scores_gemma":[0.0007916926,0.00018811051,0.00020115064,0.0018780599,0.00079078216,0.0014114226,0.00059620175,0.0013024495,0.0023578552],"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":[0.00007053069,0.000038617753,0.00029036467,0.0042496873,0.00003922582,0.0009503391,0.00009664898,0.00035216197,0.0014661128,0.004014219,0.03766255,0.9507695],"study_design_scores_gemma":[0.000029766827,0.000068156434,0.0011456927,0.0014561557,0.000054252112,0.0049312697,0.00010330314,0.000070594106,0.0003276255,0.004696623,0.9870991,0.000017489156],"about_ca_topic_score_codex":0.0010918862,"about_ca_topic_score_gemma":0.0016650781,"teacher_disagreement_score":0.0022386783,"about_ca_system_score_codex":0.00057164906,"about_ca_system_score_gemma":0.00071262865,"threshold_uncertainty_score":0.007489145},"labels":[],"label_agreement":null},{"id":"W1910203405","doi":"10.1002/047001153x.g103207","title":"Imprinting and epigenetics in mouse models and embryogenesis: understanding the requirement for both parental genomes","year":2005,"lang":"en","type":"other","venue":"Encyclopedia of Genetics, Genomics, Proteomics and Bioinformatics","topic":"Genetic Syndromes and Imprinting","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":"Western University","funders":"","keywords":"Genomic imprinting; Biology; Imprinting (psychology); Epigenetics; Genetics; Embryogenesis; Genome; Embryo; Gene; Embryonic stem cell; Parthenogenesis; X-inactivation; Cell fate determination; DNA methylation; X chromosome; Gene expression","score_opus":0.020167740544627073,"score_gpt":0.23715973019542183,"score_spread":0.21699198965079475,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1910203405","genre_codex":"review","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":[0.15193582,0.5681276,0.19638409,0.008592478,0.0011929058,0.00012439115,0.00516033,0.0044161123,0.064066224],"genre_scores_gemma":[0.37264103,0.41885465,0.12708668,0.0032092836,0.0004300059,0.00034567554,0.004944926,0.00051864487,0.071969114],"study_design_codex":"bench_or_experimental","study_design_gemma":"theoretical_or_conceptual","domain_scores_codex":[0.9998801,0.00002450409,0.000010492975,0.000025733856,0.000047476016,0.000011796658],"domain_scores_gemma":[0.999892,0.000029104116,0.000031216117,0.000018454151,0.000013270077,0.000016008875],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0004995812,0.0005156696,0.0004167014,0.0011308371,0.00015707505,0.00074677623,0.00087790395,0.0005469152,0.0030015607],"category_scores_gemma":[0.00019594561,0.00021318208,0.00023778576,0.00067003595,0.0004456549,0.00073954335,0.00056709565,0.00083128735,0.00097484177],"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":[0.0003698872,0.00010142006,0.0016593265,0.0012826654,0.00006844281,0.00092659536,0.00009806935,0.0013311071,0.71162087,0.044584062,0.011197299,0.22676033],"study_design_scores_gemma":[0.00006137625,0.0002801107,0.013054115,0.0006895471,0.00025297515,0.004744341,0.00011935555,0.0050659617,0.3064305,0.030451141,0.6387797,0.00007093954],"about_ca_topic_score_codex":0.0007077398,"about_ca_topic_score_gemma":0.001098129,"teacher_disagreement_score":0.0030015607,"about_ca_system_score_codex":0.00038110986,"about_ca_system_score_gemma":0.00025144414,"threshold_uncertainty_score":0.010041237},"labels":[],"label_agreement":null},{"id":"W1918246687","doi":"10.1002/ajmg.c.31362","title":"Molecular Mechanisms of Childhood Overgrowth","year":2013,"lang":"en","type":"article","venue":"American Journal of Medical Genetics Part C Seminars in Medical Genetics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":48,"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":"Natural Sciences and Engineering Research Council of Canada; Canadian Institutes of Health Research","keywords":"PI3K/AKT/mTOR pathway; PTEN; Gene; Biology; Somatic cell; Cell biology; Genetics; Signal transduction","score_opus":0.004497885081645766,"score_gpt":0.24888345646908588,"score_spread":0.24438557138744013,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1918246687","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":[0.018652355,0.8486344,0.003970851,0.05975125,0.025247112,0.00005482602,0.00035354838,0.00030482342,0.043030795],"genre_scores_gemma":[0.118006505,0.7928548,0.0027907644,0.0097829215,0.019740324,0.00010442531,0.00045813862,0.00006539713,0.056196705],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.99983716,0.000020776015,0.000010131747,0.00002643091,0.000062672945,0.000042807726],"domain_scores_gemma":[0.99986005,0.000034134147,0.000033864697,0.000010001903,0.00002381666,0.000038162718],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00031279976,0.0004366735,0.00028781287,0.00053649826,0.00031553375,0.0010353107,0.00055696623,0.0009971894,0.0055293753],"category_scores_gemma":[0.00034496386,0.000119822194,0.0002536449,0.00025657014,0.00082647294,0.00067980663,0.0006195578,0.0013235632,0.0011507114],"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":[0.00040732478,0.0001369263,0.0024208426,0.001465629,0.00010112637,0.0034550007,0.00042642676,0.0009377516,0.08115098,0.16962516,0.30513936,0.4347335],"study_design_scores_gemma":[0.000042094987,0.00011814741,0.005218676,0.00027461242,0.000029706773,0.0034446726,0.0001749898,0.0002520639,0.015262133,0.022101715,0.95305693,0.000024257664],"about_ca_topic_score_codex":0.00037329813,"about_ca_topic_score_gemma":0.0004641128,"teacher_disagreement_score":0.0055293753,"about_ca_system_score_codex":0.0009471636,"about_ca_system_score_gemma":0.00051646127,"threshold_uncertainty_score":0.018497586},"labels":[],"label_agreement":null},{"id":"W1944638690","doi":"10.1002/ajmg.a.37286","title":"Autism spectrum disorder in Prader–Willi syndrome: A systematic review","year":2015,"lang":"en","type":"review","venue":"American Journal of Medical Genetics Part A","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":118,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Glenrose Rehabilitation Hospital; University of Alberta; Alberta Health Services","funders":"","keywords":"Autism spectrum disorder; CINAHL; Neurodevelopmental disorder; Autism; Uniparental disomy; Medicine; Angelman syndrome; Clinical psychology; MEDLINE; Meta-analysis; Psychology; Psychiatry; Genetics; Psychological intervention; Chromosome; Pathology; Biology","score_opus":0.02094389307874395,"score_gpt":0.32905415314357767,"score_spread":0.3081102600648337,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1944638690","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":[0.0008029096,0.9980069,0.000057890175,0.00021256825,0.00008793639,0.00011031282,0.00046981595,0.0000055319924,0.0002462338],"genre_scores_gemma":[0.0065522348,0.99232095,0.0002443728,0.0002794125,0.000056717003,0.00023838977,0.00022775683,0.0000028432132,0.00007730317],"study_design_codex":"systematic_review","study_design_gemma":"systematic_review","domain_scores_codex":[0.9964948,0.0009025846,0.0015038279,0.00032338998,0.0006455309,0.00012991634],"domain_scores_gemma":[0.9834003,0.011818794,0.002872379,0.00016274874,0.0014826462,0.0002631665],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.003934045,0.0011530849,0.0059692906,0.015431186,0.000524168,0.00206785,0.0018185447,0.0016359782,0.004760682],"category_scores_gemma":[0.019818742,0.00078629353,0.004063002,0.01574483,0.0007926475,0.0023638918,0.0015213353,0.0009197968,0.00034546966],"study_design_candidate":"systematic_review","study_design_consensus":"systematic_review","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00009355857,0.00001115492,0.00088363996,0.9549818,0.0027065333,0.00014093457,0.00027498577,0.0000503335,0.00010008818,0.00020623629,0.0027758798,0.03777488],"study_design_scores_gemma":[0.000114318595,0.00009710545,0.006932243,0.9497469,0.01953235,0.0006408474,0.00042928694,0.00004737504,0.000066381086,0.00020280207,0.022162791,0.000027691813],"about_ca_topic_score_codex":0.012657808,"about_ca_topic_score_gemma":0.031823553,"teacher_disagreement_score":0.015431186,"about_ca_system_score_codex":0.0032019627,"about_ca_system_score_gemma":0.009629826,"threshold_uncertainty_score":0.0251683},"labels":[],"label_agreement":null},{"id":"W1945471693","doi":"10.1152/ajpregu.2000.279.6.r2287","title":"Intestinal transport of monosaccharides and amino acids during postnatal development of mink","year":2000,"lang":"en","type":"article","venue":"American Journal of Physiology-Regulatory, Integrative and Comparative Physiology","topic":"Genetic Syndromes and Imprinting","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":"Université de Montréal","funders":"","keywords":"Amino acid; Mink; Biology; Methionine; Biochemistry; Phenylalanine; Leucine; Brush border; Internal medicine; Endocrinology; Chemistry; Vesicle","score_opus":0.01195266600690161,"score_gpt":0.24814148793251675,"score_spread":0.23618882192561513,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1945471693","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9976217,0.0008991747,0.00046851605,0.000017690938,0.000007402457,0.000005210107,0.00025815377,0.000012011501,0.00071027846],"genre_scores_gemma":[0.9956905,0.00071674184,0.00092306116,0.00002498561,0.0000050455446,0.00002543895,0.00033374628,0.000022051508,0.002258362],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99990475,0.000006163409,0.000007427085,0.000040792795,0.000015451249,0.000025428224],"domain_scores_gemma":[0.99985933,0.000015236634,0.000050924336,0.000007447316,0.00002188245,0.000045188033],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00011179808,0.000248542,0.00028988157,0.000337658,0.00019327323,0.00033401226,0.00021392285,0.0002143479,0.00078318233],"category_scores_gemma":[0.00017443768,0.00021209194,0.00018007006,0.00019232907,0.00026174574,0.0004573083,0.00028748077,0.00043409845,0.00027050907],"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":[0.0008701165,0.000040356477,0.02365015,0.00008774558,0.000016189404,0.00034125257,0.00041153107,0.00007653817,0.96732473,0.00017617943,0.00004481165,0.0069603743],"study_design_scores_gemma":[0.000013844099,0.0008063718,0.625533,0.000021876667,0.00007983841,0.001185118,0.0006834846,0.000474188,0.3682236,0.00013641137,0.002816817,0.000025570414],"about_ca_topic_score_codex":0.0023940213,"about_ca_topic_score_gemma":0.003948421,"teacher_disagreement_score":0.0023940213,"about_ca_system_score_codex":0.00045380907,"about_ca_system_score_gemma":0.0002140132,"threshold_uncertainty_score":0.004760146},"labels":[],"label_agreement":null},{"id":"W1951209160","doi":"10.1139/bcb-2015-0032","title":"A role for chromatin topology in imprinted domain regulation","year":2015,"lang":"en","type":"review","venue":"Biochemistry and Cell Biology","topic":"Genetic Syndromes and Imprinting","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":true,"route_about_ca":false,"ca_institutions":"Children’s Health Research Institute; Western University","funders":"","keywords":"Chromatin; Scaffold/matrix attachment region; ChIA-PET; Topology (electrical circuits); Genomic imprinting; Biology; Nucleoporin; Regulation of gene expression; Computational biology; Chromosome conformation capture; Lamin; Genetics; Chromatin remodeling; Gene; Cell biology; Cell nucleus; Gene expression; DNA methylation; Nuclear transport","score_opus":0.01535157294503909,"score_gpt":0.2854822223928596,"score_spread":0.2701306494478205,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1951209160","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":[0.00025496056,0.99827445,0.0002622418,0.00021039193,0.000093286886,0.0000027720241,0.00002945107,0.000006792007,0.000865687],"genre_scores_gemma":[0.0028022646,0.9961248,0.00021988862,0.00014456076,0.00011404266,0.0000046229366,0.000059039936,0.0000019826311,0.0005288539],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.9998683,0.000023226054,0.000017955153,0.000034393255,0.000039924467,0.000016119535],"domain_scores_gemma":[0.99971944,0.00015170456,0.000040229195,0.000010698896,0.000054381995,0.000023504608],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00046243495,0.00045548694,0.0007885882,0.0013348612,0.00023087952,0.00089212495,0.0006327982,0.0008587366,0.0022634894],"category_scores_gemma":[0.0006317373,0.00022843218,0.00038162264,0.0012353607,0.00060461945,0.0009596546,0.00061842427,0.00093727664,0.0010339622],"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":[0.00010443635,0.000034662728,0.001054449,0.017912157,0.0001463796,0.0004632455,0.00015220998,0.0012681149,0.008911448,0.01670844,0.016950613,0.9362938],"study_design_scores_gemma":[0.000012663052,0.00006354592,0.002800998,0.0021136308,0.00012760622,0.0020215,0.000062429914,0.00020033968,0.0028243198,0.0054855235,0.98425716,0.000030307692],"about_ca_topic_score_codex":0.0009161155,"about_ca_topic_score_gemma":0.0012019651,"teacher_disagreement_score":0.0022634894,"about_ca_system_score_codex":0.00072313816,"about_ca_system_score_gemma":0.00086555746,"threshold_uncertainty_score":0.0075721145},"labels":[],"label_agreement":null},{"id":"W1953305292","doi":"10.1111/j.1468-3148.2011.00625.x","title":"Assessing Joint Attention Responding and Initiation in Children with Angelman Syndrome","year":2011,"lang":"en","type":"article","venue":"Journal of Applied Research in Intellectual Disabilities","topic":"Genetic Syndromes and Imprinting","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":"McMaster University; Hamilton Health Sciences; Deer Lodge Centre; McMaster Children's Hospital","funders":"","keywords":"Joint attention; Angelman syndrome; Psychology; Autism; Remedial education; Cognition; Autism spectrum disorder; Mental age; Developmental psychology; Neurodevelopmental disorder; Cognitive psychology; Psychiatry","score_opus":0.10162146939252144,"score_gpt":0.33365181758738954,"score_spread":0.23203034819486812,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1953305292","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9992518,0.000063214866,0.00012845924,0.000015525768,0.0000025256545,0.000029875344,0.000075868695,0.0000100866655,0.00042278547],"genre_scores_gemma":[0.9982754,0.00014551937,0.0010412072,0.000014035354,0.0000023786226,0.000064546,0.00022217979,0.0000036542456,0.0002311512],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9989203,0.00029127332,0.00019120924,0.00014621734,0.00026781022,0.00018320496],"domain_scores_gemma":[0.99758565,0.000659459,0.0010288445,0.00008807028,0.00031301889,0.00032496953],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0016003371,0.00086724816,0.0005729519,0.0012788945,0.00037931095,0.00059230305,0.00047878423,0.00048941304,0.0010377151],"category_scores_gemma":[0.004743772,0.00024922847,0.00043888655,0.000600808,0.0006021776,0.000380176,0.00083770603,0.00068149867,0.00022660865],"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":[0.00021443197,0.00018844783,0.9790253,0.00010623853,0.0000366052,0.0013438186,0.0033230553,0.0002560599,0.0071544475,0.000036227422,0.00018963646,0.008125658],"study_design_scores_gemma":[0.000016497364,0.0005552891,0.99119484,0.00002049038,0.000036282527,0.0030921914,0.0018964915,0.00024654216,0.0025422676,0.000051823194,0.00033248498,0.000014775117],"about_ca_topic_score_codex":0.008146449,"about_ca_topic_score_gemma":0.0116521865,"teacher_disagreement_score":0.008146449,"about_ca_system_score_codex":0.0006520874,"about_ca_system_score_gemma":0.00079625746,"threshold_uncertainty_score":0.016198039},"labels":[],"label_agreement":null},{"id":"W1964340841","doi":"10.1086/302817","title":"Identification of Novel Imprinted Transcripts in the Prader-Willi Syndrome and Angelman Syndrome Deletion Region: Further Evidence for Regional Imprinting Control","year":2000,"lang":"en","type":"article","venue":"The American Journal of Human Genetics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":50,"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":"Genomic imprinting; Angelman syndrome; Imprinting (psychology); Biology; Genetics; UBE3A; Gene; Locus (genetics); Allele; Phenotype; Gene expression; DNA methylation","score_opus":0.03826544508161572,"score_gpt":0.2959085618659046,"score_spread":0.25764311678428886,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1964340841","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9933088,0.00072527793,0.0043651466,0.00012221797,0.000020099274,0.000008540667,0.00031213558,0.000066917186,0.0010709001],"genre_scores_gemma":[0.993672,0.00026082873,0.004612787,0.000029980047,0.000022818276,0.000016326192,0.00041404928,0.00002479758,0.0009462888],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99986947,0.000015117003,0.000010126027,0.000046097244,0.00003503594,0.000024155519],"domain_scores_gemma":[0.9994666,0.00024008167,0.00013496946,0.000056380042,0.00003830029,0.00006368038],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00017732363,0.0003666565,0.00025095243,0.0004898298,0.00019914552,0.0002808877,0.00041393572,0.0003393301,0.0013748613],"category_scores_gemma":[0.0006426797,0.00029914454,0.0002850781,0.00019897603,0.00048251063,0.0002111585,0.0002744306,0.0004897411,0.00045218138],"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":[0.00017621211,0.000010154811,0.0036224853,0.000028103172,0.000014090844,0.0023876536,0.000111942514,0.00018284982,0.9907935,0.0004894676,0.000034900262,0.0021487018],"study_design_scores_gemma":[0.00014438764,0.0005218516,0.25028938,0.000024876232,0.00017853484,0.044968747,0.00034198136,0.002675794,0.6930003,0.0016587785,0.0061580925,0.000037247828],"about_ca_topic_score_codex":0.00045375826,"about_ca_topic_score_gemma":0.0010462686,"teacher_disagreement_score":0.0013748613,"about_ca_system_score_codex":0.00016263108,"about_ca_system_score_gemma":0.00017494372,"threshold_uncertainty_score":0.0045993924},"labels":[],"label_agreement":null},{"id":"W1964384703","doi":"10.4161/epi.23063","title":"Tissue-specific relationship of S-adenosylhomocysteine with allele-specific<i>H19/Igf2</i>methylation and imprinting in mice with hyperhomocysteinemia","year":2012,"lang":"en","type":"article","venue":"Epigenetics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":13,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Child and Family Research Institute; University of British Columbia","funders":"Child and Family Research Institute; University of British Columbia; Canadian Institutes of Health Research; Sick Kids Foundation; Heart and Stroke Foundation of Canada; American Heart Association","keywords":"Methylation; Genomic imprinting; Imprinting (psychology); Biology; Hyperhomocysteinemia; DNA methylation; Cystathionine beta synthase; Homocysteine; Allele; Methyltransferase; Molecular biology; Gene expression; Endocrinology; Gene; Genetics; Methionine","score_opus":0.016643573123072696,"score_gpt":0.23330077874052926,"score_spread":0.21665720561745658,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1964384703","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9963916,0.00075819757,0.0010778349,0.00010131677,0.000019333418,0.000012190934,0.0006214508,0.00011413904,0.00090395455],"genre_scores_gemma":[0.9917082,0.00051206513,0.0012022067,0.00007616114,0.000012700498,0.000034904107,0.00071787694,0.00010198769,0.0056338958],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9997086,0.000030783274,0.000023902425,0.000095974196,0.00006890391,0.00007179612],"domain_scores_gemma":[0.9994117,0.00005747068,0.00023599072,0.000034040124,0.000029416595,0.0002312996],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00013027905,0.000422116,0.00033523858,0.0010272166,0.00020076131,0.00042468825,0.00027426163,0.00042348247,0.0023649414],"category_scores_gemma":[0.00012845719,0.0004111526,0.0003110473,0.00026684883,0.00049428415,0.00020805244,0.00025049728,0.0010766663,0.00041904606],"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":[0.00043794166,0.000025891875,0.00070357963,0.000010006561,0.0000062838826,0.000043672233,0.000019585,0.00002337925,0.9980349,0.00004321253,0.000017375674,0.0006341653],"study_design_scores_gemma":[0.000037544232,0.0005949262,0.03866488,0.0000061396568,0.000044207383,0.00042650374,0.00007995706,0.00045732263,0.9586115,0.00006867867,0.0009952013,0.000013022256],"about_ca_topic_score_codex":0.0019976574,"about_ca_topic_score_gemma":0.003065643,"teacher_disagreement_score":0.0023649414,"about_ca_system_score_codex":0.0005493687,"about_ca_system_score_gemma":0.00024514756,"threshold_uncertainty_score":0.007911503},"labels":[],"label_agreement":null},{"id":"W1965277298","doi":"10.1111/j.1601-183x.2011.00678.x","title":"Imprinted<i>Rasgrf1</i>expression in neonatal mice affects olfactory learning and memory","year":2011,"lang":"en","type":"article","venue":"Genes Brain & Behavior","topic":"Genetic Syndromes and Imprinting","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":"Hospital for Sick Children","funders":"National Institute of Diabetes and Digestive and Kidney Diseases; National Cancer Institute; National Institutes of Health","keywords":"Imprinting (psychology); Genomic imprinting; Biology; Allele; Offspring; Phenotype; Weaning; Olfactory bulb; Endocrinology; Internal medicine; Genetics; Gene expression; Gene; Pregnancy; Central nervous system; Medicine","score_opus":0.01717042876871631,"score_gpt":0.2434507548125402,"score_spread":0.2262803260438239,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1965277298","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99613476,0.00063242036,0.0014436402,0.000085944754,0.00002219567,0.000012475507,0.00048828434,0.00014068073,0.0010396099],"genre_scores_gemma":[0.99056846,0.00094192196,0.002471142,0.000085892825,0.00001532794,0.00006912485,0.00050488947,0.0001231816,0.0052200276],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99972075,0.000040974955,0.00002897159,0.00006677318,0.000076433345,0.000066112414],"domain_scores_gemma":[0.9996278,0.000053901495,0.00014585069,0.000031881533,0.000017329194,0.00012326695],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00019643533,0.00067365554,0.00036225974,0.00074654067,0.00018245062,0.00032769394,0.0004403195,0.00047645663,0.002170589],"category_scores_gemma":[0.0001911271,0.0003418364,0.0002696498,0.00019221449,0.0006714996,0.0002700069,0.00034633448,0.0009837089,0.0004523163],"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":[0.00028049684,0.000037846818,0.00040036242,0.000019695433,0.000006293784,0.00016263276,0.000031654876,0.00006112744,0.9974287,0.0001256894,0.000032607677,0.001412833],"study_design_scores_gemma":[0.000024532355,0.000391834,0.008363271,0.000010224375,0.000023556386,0.00054008333,0.000054425283,0.0004419045,0.9892229,0.00009530133,0.00082284457,0.000009097537],"about_ca_topic_score_codex":0.0011064078,"about_ca_topic_score_gemma":0.0021650996,"teacher_disagreement_score":0.002170589,"about_ca_system_score_codex":0.00042792445,"about_ca_system_score_gemma":0.00033152287,"threshold_uncertainty_score":0.007261336},"labels":[],"label_agreement":null},{"id":"W1965313969","doi":"10.1006/geno.2002.6695","title":"Molecular Genetic Studies of Human Chromosome 7 in Russell–Silver Syndrome","year":2002,"lang":"en","type":"article","venue":"Genomics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":39,"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; SickKids Foundation; Hospital for Sick Children; University of Toronto","funders":"","keywords":"Biology; Haploinsufficiency; Genetics; Fluorescence in situ hybridization; Chromosomal inversion; Chromosome 7 (human); Chromosomal rearrangement; Chromosome; Gene mapping; Gene duplication; Gene; Karyotype; Phenotype","score_opus":0.020667762265171828,"score_gpt":0.25141422851481726,"score_spread":0.23074646624964543,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1965313969","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9904799,0.0026342405,0.0024321561,0.00024186293,0.00003162622,0.000015647203,0.00026409517,0.000077100616,0.0038234096],"genre_scores_gemma":[0.9954626,0.001208829,0.0020222657,0.00004949137,0.00002174044,0.00001064087,0.00031772998,0.00002095153,0.0008857787],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.99982953,0.000049249076,0.000015199143,0.000028710627,0.00004774267,0.000029394872],"domain_scores_gemma":[0.99963725,0.00017739288,0.00006851802,0.000027481396,0.000034013727,0.0000553441],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00026032786,0.00046737862,0.00037164416,0.0015112198,0.00030579846,0.00021756289,0.00055531715,0.00046190163,0.0012307268],"category_scores_gemma":[0.0005425616,0.00025913355,0.00033076454,0.00047728163,0.0006240333,0.00022816834,0.0003677978,0.00043622564,0.00030016442],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0012509952,0.000095573436,0.006897562,0.00019328785,0.00008614083,0.00974864,0.00024646468,0.0009605962,0.9665441,0.004276488,0.0002443886,0.009455791],"study_design_scores_gemma":[0.0001764055,0.00059932674,0.09278404,0.000039171046,0.00035358744,0.02129036,0.00044373723,0.0024016101,0.8685482,0.004335679,0.008982351,0.00004556127],"about_ca_topic_score_codex":0.0017198299,"about_ca_topic_score_gemma":0.001088189,"teacher_disagreement_score":0.0017198299,"about_ca_system_score_codex":0.00026921107,"about_ca_system_score_gemma":0.00023682193,"threshold_uncertainty_score":0.0041171312},"labels":[],"label_agreement":null},{"id":"W1968650685","doi":"10.1016/j.psychres.2006.11.010","title":"Parent-of-origin effect and genomic imprinting of the HTR2A receptor gene T102C polymorphism in psychosis","year":2007,"lang":"en","type":"article","venue":"Psychiatry Research","topic":"Genetic Syndromes and Imprinting","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":"Centre for Addiction and Mental Health; University of Toronto","funders":"","keywords":"Allele; Genomic imprinting; Imprinting (psychology); Psychosis; Locus (genetics); Genetics; Bipolar disorder; Gene; Biology; Gene expression; Psychology; Endocrinology; Psychiatry","score_opus":0.024107403603671754,"score_gpt":0.3393161368432285,"score_spread":0.3152087332395567,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1968650685","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99868315,0.0002210736,0.00029760794,0.00012784073,0.000017355367,0.000004045569,0.00013842351,0.000013233937,0.0004971287],"genre_scores_gemma":[0.9993954,0.00009360073,0.00011758717,0.000020126927,0.000020128422,0.000002586179,0.000049645358,0.000011369837,0.0002894511],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99925774,0.00034553313,0.000054636854,0.00013456022,0.00013706968,0.00007030661],"domain_scores_gemma":[0.9974776,0.001403254,0.00047095417,0.00022875553,0.0001189543,0.0003005332],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00053046807,0.0005247591,0.00046135488,0.0011894539,0.00041380868,0.0003990318,0.0004313627,0.00074434985,0.005029022],"category_scores_gemma":[0.0022337374,0.00031781435,0.00047058932,0.0007965948,0.0005797032,0.00018116037,0.00032194352,0.00066216616,0.00034575813],"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":[0.015418246,0.00053926493,0.5487459,0.00011616804,0.0011138398,0.03269752,0.0020023198,0.0010638207,0.37229148,0.0017889184,0.00067329634,0.02354927],"study_design_scores_gemma":[0.00024886636,0.0008235489,0.96739936,0.000028041932,0.00060509116,0.015135951,0.00026631946,0.0017855783,0.012385426,0.00063304213,0.00064211374,0.000046620567],"about_ca_topic_score_codex":0.00360916,"about_ca_topic_score_gemma":0.0024929186,"teacher_disagreement_score":0.005029022,"about_ca_system_score_codex":0.00025385633,"about_ca_system_score_gemma":0.00026816485,"threshold_uncertainty_score":0.016823769},"labels":[],"label_agreement":null},{"id":"W1968720872","doi":"10.1002/ajmg.a.36790","title":"Prader–Willi syndrome and Tay–Sachs disease in association with mixed maternal uniparental isodisomy and heterodisomy 15 in a girl who also had isochromosome Xq","year":2014,"lang":"en","type":"article","venue":"American Journal of Medical Genetics Part A","topic":"Genetic Syndromes and Imprinting","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":"Hamilton Health Sciences; St. Joseph’s Healthcare Hamilton; Hamilton Regional Laboratory Medicine Program; McMaster University","funders":"","keywords":"Girl; Isochromosome; Association (psychology); Medicine; Genetics; Tay-Sachs disease; Pediatrics; Psychology; Disease; Biology; Internal medicine; Karyotype; Chromosome; Gene","score_opus":0.004336278804184094,"score_gpt":0.2275572275702251,"score_spread":0.22322094876604098,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1968720872","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9985487,0.0002289149,0.00045494566,0.00012021854,0.000012938546,0.000015269065,0.000064349144,0.000017893617,0.00053671],"genre_scores_gemma":[0.99884737,0.00017964818,0.00044896992,0.000027864031,0.000026060263,0.000009241169,0.000037518257,0.0000058026762,0.00041749637],"study_design_codex":"case_report","study_design_gemma":"case_report","domain_scores_codex":[0.99967635,0.00004861302,0.00003077785,0.00011225242,0.00007155874,0.000060548886],"domain_scores_gemma":[0.99968743,0.000086095126,0.000105469764,0.000018037177,0.000014564108,0.00008846472],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00020482148,0.0010684518,0.0004026391,0.0013799808,0.0005748895,0.00028606178,0.00046086832,0.00074907986,0.0020587153],"category_scores_gemma":[0.0009935508,0.0005605849,0.00032976866,0.0005459769,0.00070339104,0.00030498844,0.00059144443,0.00076732825,0.00033036084],"study_design_candidate":"case_report","study_design_consensus":"case_report","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00047509136,0.00016482775,0.21120465,0.00007996985,0.00014041264,0.7232417,0.0010381305,0.00026344953,0.055605657,0.0008372712,0.00038460572,0.006564191],"study_design_scores_gemma":[0.000049129147,0.00046735088,0.14766796,0.000025841484,0.000108358916,0.84237736,0.00023435031,0.0007758408,0.0071321316,0.00025694692,0.00088289723,0.000021794523],"about_ca_topic_score_codex":0.0013944136,"about_ca_topic_score_gemma":0.0023748688,"teacher_disagreement_score":0.0020587153,"about_ca_system_score_codex":0.0002398572,"about_ca_system_score_gemma":0.00030002938,"threshold_uncertainty_score":0.0068870783},"labels":[],"label_agreement":null},{"id":"W1969373798","doi":"10.1159/000083333","title":"Genetic Diversity among the Arabs","year":2005,"lang":"en","type":"review","venue":"Public Health Genomics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":88,"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; Hospital for Sick Children","funders":"","keywords":"Consanguinity; Founder effect; Population; Genetics; Genetic heterogeneity; Medicine; Demography; Biology; Allele; Environmental health; Haplotype; Gene; Phenotype","score_opus":0.06483115023011855,"score_gpt":0.3099430890941076,"score_spread":0.24511193886398908,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1969373798","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":[0.00083763426,0.9957681,0.00011420292,0.00056813733,0.00015353736,0.0000031838567,0.000026734611,0.0000080452655,0.0025204895],"genre_scores_gemma":[0.004394308,0.9941553,0.00014015383,0.00019271592,0.00020904538,0.000004515944,0.000050513056,8.1069714e-7,0.0008525786],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.9998437,0.00003964674,0.000019861016,0.000036455524,0.000044431727,0.000015758853],"domain_scores_gemma":[0.99984384,0.00006286301,0.000025626392,0.000005489896,0.000044823366,0.000017316714],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00045666684,0.0005772433,0.0010274128,0.0014100872,0.0002399178,0.0007076349,0.00038389533,0.0006246685,0.0025649397],"category_scores_gemma":[0.0006550523,0.00011320695,0.0002478536,0.0013105308,0.00037273022,0.00055919186,0.00036200948,0.00045507526,0.0012036179],"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":[0.000043200667,0.00002095263,0.0014039088,0.0023920329,0.00005714814,0.0003831989,0.00008032018,0.00012424416,0.0005823737,0.0010047413,0.013829753,0.9800781],"study_design_scores_gemma":[0.00004523909,0.00020138492,0.017946372,0.006587512,0.0002507251,0.012094221,0.00046108305,0.00012988185,0.0008909142,0.0041449894,0.9572059,0.000041686933],"about_ca_topic_score_codex":0.001702396,"about_ca_topic_score_gemma":0.0019403906,"teacher_disagreement_score":0.0025649397,"about_ca_system_score_codex":0.0004137391,"about_ca_system_score_gemma":0.0005514391,"threshold_uncertainty_score":0.008580565},"labels":[],"label_agreement":null},{"id":"W1969676656","doi":"10.2350/13-02-1300-cr.1","title":"Nested Stromal Epithelial Tumor of the Liver in Beckwith-Wiedemann Syndrome","year":2013,"lang":"en","type":"article","venue":"Pediatric and Developmental Pathology","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":27,"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 Research Chairs; Hospital for Sick Children; London Health Sciences Centre; University of Toronto","funders":"","keywords":"Hepatoblastoma; Pathology; Medicine; Beckwith–Wiedemann syndrome; Wilms' tumor; CD117; Stromal tumor; Abdominal mass; Malignancy; Liver tumor; Stromal cell; Hepatocellular carcinoma; Internal medicine; Biology","score_opus":0.005840488438307744,"score_gpt":0.18793312557421915,"score_spread":0.1820926371359114,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1969676656","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99686134,0.0005882387,0.000904128,0.00013917303,0.000022881299,0.000013871461,0.00009406228,0.000053035525,0.0013232733],"genre_scores_gemma":[0.9990482,0.00019735946,0.0005738552,0.00002124274,0.000013868336,0.0000027383403,0.000027081638,0.0000035661699,0.000112218804],"study_design_codex":"case_report","study_design_gemma":"case_report","domain_scores_codex":[0.99984455,0.00002300245,0.00002179796,0.000038310063,0.000030335535,0.0000419035],"domain_scores_gemma":[0.9995228,0.00014365013,0.00014390901,0.00002348502,0.00002261925,0.00014352128],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00013825634,0.0005176081,0.00022093451,0.0009788424,0.00040727484,0.00030678516,0.00017828897,0.0005331191,0.0011353294],"category_scores_gemma":[0.0008980476,0.00034576262,0.00024939416,0.00046802592,0.00052774244,0.0003244436,0.00053716655,0.00042721484,0.00018220514],"study_design_candidate":"case_report","study_design_consensus":"case_report","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00008694894,0.000021831469,0.07826754,0.000058364898,0.000022843886,0.9036382,0.00021031122,0.0002255331,0.013399946,0.00054078747,0.0002537181,0.0032738931],"study_design_scores_gemma":[0.000010423191,0.00007122401,0.0461622,0.000013022654,0.000026214873,0.94902945,0.00012536626,0.0004077283,0.0033749442,0.000196022,0.0005726663,0.000010712817],"about_ca_topic_score_codex":0.0013027367,"about_ca_topic_score_gemma":0.0018172606,"teacher_disagreement_score":0.0013027367,"about_ca_system_score_codex":0.00028373266,"about_ca_system_score_gemma":0.00024735124,"threshold_uncertainty_score":0.003798008},"labels":[],"label_agreement":null},{"id":"W1969702194","doi":"10.1016/j.ando.2015.03.028","title":"Pseudohypoparathyroidism type Ib in 2015","year":2015,"lang":"fr","type":"review","venue":"Annales d Endocrinologie","topic":"Genetic Syndromes and Imprinting","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":"Ministry of Health, British Columbia; Ministero della Salute","keywords":"GNAS complex locus; Pseudohypoparathyroidism; Brachydactyly; Short stature; Osteodystrophy; Endocrinology; Parathyroid hormone; Internal medicine; Medicine; Genetics; Biology; Gene","score_opus":0.1011404986461075,"score_gpt":0.36225239294170747,"score_spread":0.2611118942956,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1969702194","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":[0.00031438118,0.9965707,0.00018045836,0.0007993642,0.00052425376,0.0000034651518,0.00005373101,0.000008665908,0.0015449809],"genre_scores_gemma":[0.0035594364,0.99245465,0.00030101868,0.00092823076,0.0011183283,0.0000065545046,0.00016923647,0.000004166257,0.0014584053],"study_design_codex":"design_other","study_design_gemma":"theoretical_or_conceptual","domain_scores_codex":[0.9998727,0.00001741167,0.000025993588,0.000025747708,0.00004285332,0.00001526258],"domain_scores_gemma":[0.99981505,0.00008529015,0.000037115668,0.000006745291,0.00002989244,0.000025976378],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00031061436,0.00051501626,0.0007538376,0.001771113,0.00020080821,0.00057544507,0.0005115094,0.000811093,0.0023376266],"category_scores_gemma":[0.0008137341,0.00015498887,0.0002668511,0.0011442155,0.00044532286,0.000742129,0.0005842179,0.0012535158,0.0009379686],"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":[0.00012462928,0.000026645896,0.0011389111,0.0060227197,0.0000873652,0.004013052,0.000074183794,0.0002631908,0.001015959,0.0046244627,0.059490945,0.92311794],"study_design_scores_gemma":[0.000028143773,0.000034619283,0.002352779,0.0029076878,0.00016004588,0.024331003,0.00007338106,0.00007454382,0.0004066996,0.0019332239,0.96767366,0.000024204044],"about_ca_topic_score_codex":0.002105593,"about_ca_topic_score_gemma":0.0040672724,"teacher_disagreement_score":0.0023376266,"about_ca_system_score_codex":0.00058586145,"about_ca_system_score_gemma":0.001060942,"threshold_uncertainty_score":0.007820189},"labels":[],"label_agreement":null},{"id":"W1969874642","doi":"10.1002/ajmg.c.10013","title":"Mental deficiency, alterations in performance, and CNS abnormalities in Overgrowth syndromes","year":2003,"lang":"en","type":"review","venue":"American Journal of Medical Genetics Part C Seminars in Medical Genetics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":51,"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":"","keywords":"Macrocephaly; Proteus syndrome; Costello syndrome; Sotos syndrome; Medicine; Genetic syndromes; Hypoglycemia; Autism; Epilepsy; Neurofibromatosis; Pediatrics; Internal medicine; Endocrinology; Pathology; Diabetes mellitus; Psychiatry; Cancer","score_opus":0.018004094589624917,"score_gpt":0.31456919267068306,"score_spread":0.29656509808105813,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1969874642","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":[0.0001838259,0.9965947,0.00023251295,0.00027051006,0.00036930823,0.0000035775736,0.000012122413,0.00001789241,0.0023154418],"genre_scores_gemma":[0.0011416394,0.9958878,0.00035134013,0.00028961577,0.0002921992,0.000006627127,0.000031360312,0.000002537049,0.0019968715],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.999859,0.000022625347,0.000020534904,0.00002649491,0.000056203076,0.0000151386],"domain_scores_gemma":[0.99982905,0.00007096199,0.000022389251,0.000008039687,0.000041443553,0.000028071327],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0003624344,0.0011931465,0.0016874672,0.0027601859,0.00031870583,0.0008634865,0.0009943126,0.0010882543,0.002857004],"category_scores_gemma":[0.0005096489,0.00024821423,0.00026959684,0.0030735924,0.00071476266,0.001326707,0.000590872,0.0012854304,0.0031341312],"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":[0.00006945992,0.00006326329,0.00048826158,0.0042284746,0.00006241746,0.0016259431,0.000090813395,0.0002845362,0.0014973747,0.0034221278,0.05688052,0.93128675],"study_design_scores_gemma":[0.000022196864,0.000044569293,0.001753293,0.0014622902,0.000069287824,0.00959175,0.00012950189,0.00006674449,0.00031848758,0.0022060308,0.9843158,0.000019944922],"about_ca_topic_score_codex":0.0014004275,"about_ca_topic_score_gemma":0.0026045118,"teacher_disagreement_score":0.002857004,"about_ca_system_score_codex":0.0006206216,"about_ca_system_score_gemma":0.000751268,"threshold_uncertainty_score":0.009557605},"labels":[],"label_agreement":null},{"id":"W1970011619","doi":"10.4161/epi.3.6.7109","title":"Novel imprinted transcripts from the<i>Dlk1-Gtl2</i>intergenic region,<i>Mico1</i>and<i>Mico1os</i>, show circadian oscillations","year":2008,"lang":"en","type":"article","venue":"Epigenetics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","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":"Douglas Mental Health University Institute; McGill University","funders":"Eunice Kennedy Shriver National Institute of Child Health and Human Development; Canadian Institutes of Health Research","keywords":"Genomic imprinting; Biology; Intergenic region; Genetics; Transcription (linguistics); Gene; Circadian rhythm; Imprinting (psychology); Chromosome; Genome; Gene expression; DNA methylation; Neuroscience","score_opus":0.02562780136574606,"score_gpt":0.2236606763590861,"score_spread":0.19803287499334005,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1970011619","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99483323,0.0006654233,0.002454789,0.000028260281,0.0000125335,0.0000136083345,0.00094651105,0.000044289078,0.0010013455],"genre_scores_gemma":[0.992074,0.0003468081,0.0033796374,0.000037804955,0.000013153181,0.00002822216,0.0023314238,0.00002585549,0.0017630889],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99992836,0.0000036401404,0.000003781038,0.00003167875,0.000015926478,0.000016514532],"domain_scores_gemma":[0.99982506,0.000033338925,0.0000814566,0.000013375964,0.000011890342,0.00003496926],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.000050398092,0.00023024993,0.00012208667,0.000298065,0.00009907126,0.00016804166,0.00012594865,0.00013755163,0.0010422351],"category_scores_gemma":[0.00014730445,0.0000988923,0.0001380403,0.00017470834,0.00018103656,0.000090614354,0.00015114783,0.00020073986,0.00020417024],"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":[0.00009715696,0.0000055678142,0.0032766268,0.000028302264,0.0000036083836,0.00015722468,0.000028636894,0.000026094289,0.9941757,0.00007114463,0.000023765215,0.0021061874],"study_design_scores_gemma":[0.00002767007,0.00031121558,0.2620359,0.000014491769,0.000051872677,0.003345141,0.00013457764,0.00056250073,0.7272068,0.00022269614,0.0060729375,0.000014220827],"about_ca_topic_score_codex":0.00027363087,"about_ca_topic_score_gemma":0.0008101233,"teacher_disagreement_score":0.0010422351,"about_ca_system_score_codex":0.00016240033,"about_ca_system_score_gemma":0.00009718785,"threshold_uncertainty_score":0.0034866333},"labels":[],"label_agreement":null},{"id":"W1970069693","doi":"10.1371/journal.pone.0101012","title":"Clinically Important Age-Related Differences in Sleep Related Disordered Breathing in Infants and Children with Prader-Willi Syndrome","year":2014,"lang":"en","type":"article","venue":"PLoS ONE","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":118,"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":"","keywords":"Polysomnogram; Medicine; Pediatrics; Obstructive sleep apnea; Apnea; Polysomnography; Central sleep apnea; Sleep apnea; Population; Internal medicine","score_opus":0.012072076897587571,"score_gpt":0.20838486092879188,"score_spread":0.1963127840312043,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1970069693","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99934953,0.00029430352,0.000035311896,0.000014539109,0.000003566504,0.0000052616097,0.00006524377,0.0000014889806,0.00023072674],"genre_scores_gemma":[0.9995233,0.00017615587,0.00006488947,0.000011817329,0.0000079082465,0.000008637872,0.00015230969,0.0000013798614,0.00005357332],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99963427,0.00008659184,0.000050331528,0.00006816132,0.00008578796,0.00007492006],"domain_scores_gemma":[0.99877745,0.00033776663,0.00059213844,0.000037089278,0.000072777366,0.00018288709],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0004186831,0.0002461845,0.00028042265,0.0007405254,0.00019668817,0.00025685504,0.00018451623,0.00032237163,0.0010230464],"category_scores_gemma":[0.0028005394,0.000135018,0.00024082717,0.00042788015,0.00027260958,0.00031827312,0.00033005833,0.0003048649,0.00014700502],"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":[0.00012835648,0.000014430592,0.99662304,0.000010623649,0.00001665932,0.0005893928,0.00009621968,0.000028216647,0.0006809428,0.000015026018,0.000035480385,0.0017615344],"study_design_scores_gemma":[0.0000018056702,0.00008615526,0.99811375,0.0000023379882,0.000004692315,0.0015905371,0.000084506835,0.0000233169,0.000043028827,0.0000054645316,0.000043413067,0.0000010142231],"about_ca_topic_score_codex":0.0011183992,"about_ca_topic_score_gemma":0.0016376863,"teacher_disagreement_score":0.0011183992,"about_ca_system_score_codex":0.0002089797,"about_ca_system_score_gemma":0.00016702806,"threshold_uncertainty_score":0.003422439},"labels":[],"label_agreement":null},{"id":"W1970925597","doi":"10.1002/ijc.20280","title":"Allelic loss but absence of mutations in the polyspecific transporter gene <i>BWR1A</i> on 11p15.5 in hepatoblastoma","year":2004,"lang":"en","type":"article","venue":"International Journal of Cancer","topic":"Genetic Syndromes and Imprinting","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":"McGill University; Jewish General Hospital","funders":"","keywords":"Hepatoblastoma; Biology; Molecular biology; Allele; Loss of heterozygosity; Exon; Locus (genetics); Gene; Hepatocellular carcinoma; Tumor suppressor gene; Southern blot; Cancer research; Genetics; Carcinogenesis; Internal medicine; Medicine","score_opus":0.010240876873024702,"score_gpt":0.27786967359744685,"score_spread":0.26762879672442214,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1970925597","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99954504,0.00007310831,0.00020289437,0.0000043032974,5.4119994e-7,0.0000017280305,0.00004645346,0.000004907406,0.00012098197],"genre_scores_gemma":[0.9996092,0.00004880824,0.000126665,0.000003903235,0.0000010009959,0.000001959442,0.000105732805,0.000002626137,0.00010021489],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9998455,0.000027060249,0.000024991936,0.000043278545,0.00003489402,0.000024123608],"domain_scores_gemma":[0.9997111,0.000074946394,0.00012530087,0.000023806526,0.000017189193,0.00004766301],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00014553068,0.00017368022,0.00014224781,0.0005064348,0.000085523454,0.00018756175,0.00013129532,0.00014434876,0.0007193331],"category_scores_gemma":[0.000381118,0.00015991605,0.00011763787,0.0002522163,0.00027589264,0.00007356293,0.00016024773,0.0001390858,0.00020065719],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00085091963,0.000050700804,0.34099892,0.00007567391,0.00009895101,0.007996643,0.00034161366,0.00041503567,0.6370324,0.00014709163,0.00009526795,0.011896777],"study_design_scores_gemma":[0.00002577145,0.00034781374,0.89011675,0.00000925029,0.000082782724,0.028589576,0.00014239115,0.0007249351,0.07903424,0.00007650662,0.00083701254,0.000012927691],"about_ca_topic_score_codex":0.00072249613,"about_ca_topic_score_gemma":0.0010203714,"teacher_disagreement_score":0.00072249613,"about_ca_system_score_codex":0.00010575803,"about_ca_system_score_gemma":0.000059515645,"threshold_uncertainty_score":0.0024064183},"labels":[],"label_agreement":null},{"id":"W1971653306","doi":"10.1016/s0002-9440(10)64652-4","title":"p57KIP2 Is Not Mutated in Hepatoblastoma but Shows Increased Transcriptional Activity in a Comparative Analysis of the Three Imprinted Genes p57KIP2, IGF2, and H19","year":2000,"lang":"en","type":"article","venue":"American Journal Of Pathology","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":53,"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; Montreal Children's Hospital","funders":"Deutsche Forschungsgemeinschaft","keywords":"Loss of heterozygosity; Hepatoblastoma; Biology; Locus (genetics); Allele; Gene; Molecular biology; Tumor suppressor gene; Cancer research; Genetics; Carcinogenesis; Internal medicine","score_opus":0.012686565279806895,"score_gpt":0.2579052578158719,"score_spread":0.24521869253606504,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1971653306","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9982039,0.00045586439,0.0004122158,0.000025067533,0.000007076903,0.0000021595708,0.00017723854,0.000020511412,0.00069598947],"genre_scores_gemma":[0.99762124,0.00022103533,0.00031087673,0.000013984138,0.0000041249646,0.000004802049,0.0004768186,0.0000108916665,0.0013362931],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9998958,0.000009000356,0.000007726502,0.000023613553,0.000031882537,0.000032032916],"domain_scores_gemma":[0.9998246,0.00003821537,0.000040494142,0.00001627074,0.000011480256,0.000068974565],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00007782003,0.00026290724,0.00019318738,0.0009532896,0.00020367812,0.0002397849,0.00017392896,0.00016330907,0.0016766695],"category_scores_gemma":[0.00014501053,0.00023808953,0.00021766954,0.00035725033,0.00030983088,0.00015044729,0.00017570118,0.0003231061,0.0003036628],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00027494703,0.0000127302,0.0017900832,0.000012056644,0.0000103830735,0.0002680587,0.000016580194,0.000037675454,0.99677676,0.00007801958,0.000021560918,0.00070118916],"study_design_scores_gemma":[0.00003747882,0.00026488723,0.1357604,0.00000480411,0.00004690213,0.0042752638,0.00010135083,0.0005996748,0.85716784,0.00011619919,0.0016178164,0.000007371485],"about_ca_topic_score_codex":0.0011693939,"about_ca_topic_score_gemma":0.0015342495,"teacher_disagreement_score":0.0016766695,"about_ca_system_score_codex":0.00029265432,"about_ca_system_score_gemma":0.00012173361,"threshold_uncertainty_score":0.0056090355},"labels":[],"label_agreement":null},{"id":"W1972060342","doi":"10.1097/mph.0b013e3181dccd1e","title":"Simultaneous Occurrence of Pancreatoblastoma and Neuroblastoma in a Newborn With Beckwith-Wiedemann Syndrome","year":2010,"lang":"en","type":"article","venue":"Journal of Pediatric Hematology/Oncology","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":20,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Pediatric Oncology Group","funders":"","keywords":"Beckwith–Wiedemann syndrome; Medicine; Neuroblastoma; Pediatrics; Genetics","score_opus":0.005851744240814266,"score_gpt":0.24857802119655317,"score_spread":0.2427262769557389,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1972060342","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99516654,0.0012970724,0.0012796262,0.0004987379,0.00009945477,0.000021545557,0.00009352664,0.000060911432,0.0014825511],"genre_scores_gemma":[0.9976888,0.0008262295,0.0010304076,0.00010847876,0.000075138385,0.000009328379,0.000045115397,0.000008569513,0.00020786854],"study_design_codex":"case_report","study_design_gemma":"case_report","domain_scores_codex":[0.99958974,0.00005633979,0.00006771544,0.00009442035,0.00007980298,0.00011198898],"domain_scores_gemma":[0.99901533,0.00029982964,0.00023367083,0.000042852032,0.00005036152,0.0003579208],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00025950096,0.00080383423,0.0007044338,0.0013110009,0.0010831712,0.00048712056,0.0003461285,0.0012619976,0.0009878954],"category_scores_gemma":[0.0024513158,0.0004576766,0.00038594988,0.0006731671,0.00092057936,0.0005963967,0.00093447947,0.0009432292,0.00016757779],"study_design_candidate":"case_report","study_design_consensus":"case_report","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00004581648,0.000011836334,0.033070132,0.000019977215,0.000008901373,0.9627881,0.0001606336,0.00007798723,0.0019015847,0.00018897072,0.000124461,0.0016016392],"study_design_scores_gemma":[0.0000037277657,0.00006214027,0.014566497,0.00001551434,0.000021280852,0.9837907,0.00013203207,0.00015285624,0.0009121598,0.00009613402,0.00023500412,0.0000118766675],"about_ca_topic_score_codex":0.002872039,"about_ca_topic_score_gemma":0.0041361144,"teacher_disagreement_score":0.002872039,"about_ca_system_score_codex":0.00057652546,"about_ca_system_score_gemma":0.00080988207,"threshold_uncertainty_score":0.0057106614},"labels":[],"label_agreement":null},{"id":"W1972213660","doi":"10.4161/epi.4.2.7954","title":"Temporal stability and age-related prevalence of loss of imprinting of the insulin-like growth factor-2 gene","year":2009,"lang":"en","type":"article","venue":"Epigenetics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":28,"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":"National Center for Research Resources; National Cancer Institute; National Institutes of Health","keywords":"Imprinting (psychology); Genomic imprinting; Epigenetics; Insulin-like growth factor 2; Biology; Allele; Colorectal cancer; Internal medicine; Genetics; Gene; Cancer; DNA methylation; Gene expression; Medicine","score_opus":0.011882103867257406,"score_gpt":0.23128833388590742,"score_spread":0.21940623001865,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1972213660","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9991227,0.00031837064,0.00013082751,0.000009275711,0.0000027180909,0.0000027136334,0.00014480083,0.000004269625,0.00026431715],"genre_scores_gemma":[0.9996239,0.000067339926,0.000058357156,0.0000051548923,0.000004977023,0.0000031596628,0.00014844675,0.000001185425,0.000087475324],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9996723,0.000073440766,0.000038319282,0.00011144695,0.000048601418,0.000055886936],"domain_scores_gemma":[0.99727017,0.00089430646,0.0012170231,0.000142871,0.00031599792,0.00015965065],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00055536267,0.00010844077,0.00014813,0.000782313,0.00017870973,0.00031195933,0.0002109492,0.00030665504,0.0016175214],"category_scores_gemma":[0.0031506093,0.00014415398,0.000112026566,0.0005392524,0.00023330329,0.00029919928,0.00023538682,0.00027560478,0.0002808719],"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":[0.00039302235,0.000014949924,0.99502784,0.000009179295,0.000028042126,0.00008741416,0.0001277776,0.000028529015,0.0019281518,0.000012713016,0.000050488485,0.0022919206],"study_design_scores_gemma":[0.0000037098916,0.00011495505,0.99867743,0.0000021492924,0.000013611385,0.0005463998,0.00009190152,0.00009000382,0.00033768485,0.000010877172,0.00010902497,0.0000021706594],"about_ca_topic_score_codex":0.0013360674,"about_ca_topic_score_gemma":0.0010683617,"teacher_disagreement_score":0.0016175214,"about_ca_system_score_codex":0.00012339905,"about_ca_system_score_gemma":0.000088201596,"threshold_uncertainty_score":0.005411148},"labels":[],"label_agreement":null},{"id":"W1973288730","doi":"10.1002/ajmg.1356","title":"Aggressive behavior and Brunner Syndrome: No evidence for the C936T mutation in a population sample","year":2001,"lang":"en","type":"letter","venue":"American Journal of Medical Genetics","topic":"Genetic Syndromes and Imprinting","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":"Université de Montréal; McGill University","funders":"Medical Research Council; Pan American Health Organization","keywords":"Population; Library science; Psychology; Sociology; Demography; Computer science","score_opus":0.02442307126887433,"score_gpt":0.32129385469764515,"score_spread":0.2968707834287708,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1973288730","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.7678838,0.0018353297,0.0010360351,0.19720781,0.0041195974,0.000052206695,0.00092909497,0.00018994248,0.026746122],"genre_scores_gemma":[0.94372475,0.0013571547,0.0004303671,0.04109059,0.006840998,0.00003454786,0.0002481063,0.000062907224,0.006210628],"study_design_codex":"case_report","study_design_gemma":"observational","domain_scores_codex":[0.9994456,0.00013585859,0.000066129396,0.00012931097,0.00012825131,0.00009492223],"domain_scores_gemma":[0.99784374,0.0012348668,0.0002063211,0.00011964283,0.00022071511,0.00037482224],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00055480003,0.0006771959,0.0009945168,0.0007493761,0.0012991497,0.0006973496,0.0009897561,0.009096785,0.004544783],"category_scores_gemma":[0.006871385,0.0003859951,0.0004264397,0.0007364369,0.0011095331,0.0008003364,0.00028014657,0.003215859,0.00086629746],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0017594814,0.00037916965,0.42260635,0.00020031608,0.0003370882,0.44395092,0.0025113227,0.00043685114,0.008063474,0.0032565277,0.08958434,0.026914101],"study_design_scores_gemma":[0.0006068441,0.0010312276,0.44542933,0.00021149934,0.00052922335,0.49676487,0.0024369338,0.0030199983,0.0016647679,0.0053707445,0.04274875,0.00018576291],"about_ca_topic_score_codex":0.007511128,"about_ca_topic_score_gemma":0.008266956,"teacher_disagreement_score":0.009096785,"about_ca_system_score_codex":0.00064023916,"about_ca_system_score_gemma":0.00056444923,"threshold_uncertainty_score":0.015203834},"labels":[],"label_agreement":null},{"id":"W1973753171","doi":"10.1016/j.jval.2011.08.525","title":"PND59 A Common Road Map for Rational Clinical and Policy Decisionmaking: Application of the MCDA-Based Evidem Framework to Growth Hormone Use in Patients with Prader-Willi Syndrome","year":2011,"lang":"en","type":"article","venue":"Value in Health","topic":"Genetic Syndromes and Imprinting","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":"Centre Hospitalier Universitaire Sainte-Justine; Université de Montréal","funders":"","keywords":"Multiple-criteria decision analysis; Context (archaeology); Stakeholder; Population; Medicine; Scientific evidence; Psychology; Operations research; Political science; Geography; Public relations; Environmental health; Engineering","score_opus":0.05530843422811118,"score_gpt":0.33005054087963487,"score_spread":0.2747421066515237,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1973753171","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":[0.013526696,0.00593255,0.32366806,0.6080458,0.001531624,0.0021264888,0.000813453,0.00017047714,0.04418479],"genre_scores_gemma":[0.4829676,0.0026134872,0.48269877,0.025930433,0.0011275808,0.002512556,0.00036235485,0.000063127765,0.0017242429],"study_design_codex":"theoretical_or_conceptual","study_design_gemma":"theoretical_or_conceptual","domain_scores_codex":[0.8326005,0.13933153,0.0092725605,0.004172885,0.011731261,0.0028912725],"domain_scores_gemma":[0.80816007,0.15512535,0.006263663,0.0061026504,0.017003393,0.0073448834],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.15222444,0.0015189543,0.0054893577,0.008035974,0.0043269023,0.01979196,0.0061194366,0.017787294,0.006821583],"category_scores_gemma":[0.24960043,0.0017115453,0.0034204714,0.0038486249,0.016713886,0.011840366,0.01643301,0.018218106,0.00082385],"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":[0.0001816133,0.00016766781,0.0016185173,0.001093198,0.00044853694,0.0005789664,0.0014671071,0.016694607,0.00013459529,0.91613054,0.014806332,0.046678457],"study_design_scores_gemma":[0.00014097065,0.000054653396,0.00030509246,0.0013048506,0.00008723873,0.00008974682,0.00049936865,0.010608629,0.00010373697,0.9767854,0.009967718,0.000052562013],"about_ca_topic_score_codex":0.010167561,"about_ca_topic_score_gemma":0.0133607155,"teacher_disagreement_score":0.15222444,"about_ca_system_score_codex":0.015786635,"about_ca_system_score_gemma":0.046563044,"threshold_uncertainty_score":0.8050494},"labels":[],"label_agreement":null},{"id":"W1974350437","doi":"10.1158/0008-5472.can-06-0037","title":"The c-Myc Oncogene Directly Induces the H19 Noncoding RNA by Allele-Specific Binding to Potentiate Tumorigenesis","year":2006,"lang":"en","type":"article","venue":"Cancer Research","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":457,"is_retracted":false,"has_abstract":true,"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; University of Toronto; Ontario Institute for Cancer Research","funders":"","keywords":"Biology; Gene knockdown; Genomic imprinting; Chromatin immunoprecipitation; Cancer research; Carcinogenesis; Long non-coding RNA; Oncogene; Transcription factor; Gene; Gene expression; Molecular biology; RNA; Genetics; Promoter; DNA methylation; Cell cycle","score_opus":0.039916658065585,"score_gpt":0.336401392140191,"score_spread":0.29648473407460596,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1974350437","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.98614097,0.0021596176,0.0062173414,0.0001830111,0.00006363719,0.00007196481,0.00043136204,0.00022031293,0.004511789],"genre_scores_gemma":[0.99372476,0.00074354134,0.0022504688,0.000075700154,0.000016740087,0.00003376325,0.00038545256,0.000034945675,0.0027347165],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9998516,0.000022458831,0.000009117265,0.00003163942,0.000048970414,0.000036215806],"domain_scores_gemma":[0.9998865,0.000031841344,0.000026857271,0.000016341837,0.000008272286,0.00003028169],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00010776403,0.0003034877,0.0001288118,0.00028511861,0.00015353429,0.000172914,0.0001877269,0.00020211596,0.002005489],"category_scores_gemma":[0.00008785189,0.00013893958,0.0002181106,0.00010791457,0.0002164491,0.000099529374,0.0002993451,0.00059160235,0.00038032283],"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":[0.000030149868,0.000017125698,0.00008833316,0.000011959141,0.0000025139113,0.000023569788,0.0000037431994,0.000024644663,0.99904436,0.00008327226,0.000030458405,0.0006398549],"study_design_scores_gemma":[0.000008234363,0.0001533085,0.0029930605,0.0000027871838,0.0000068855293,0.00014499213,0.000006213928,0.00044470312,0.9938685,0.000023877965,0.0023452297,0.0000020665632],"about_ca_topic_score_codex":0.00056765834,"about_ca_topic_score_gemma":0.0014362009,"teacher_disagreement_score":0.002005489,"about_ca_system_score_codex":0.00028665914,"about_ca_system_score_gemma":0.00015323637,"threshold_uncertainty_score":0.006709039},"labels":[],"label_agreement":null},{"id":"W1974744326","doi":"10.1002/ajmg.a.33065","title":"Screening of DNA methylation at the H19 promoter or the distal region of its ICR1 ensures efficient detection of chromosome 11p15 epimutations in Russell–Silver syndrome","year":2009,"lang":"en","type":"article","venue":"American Journal of Medical Genetics Part A","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":110,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"North York General Hospital; University of Toronto; Hospital for Sick Children","funders":"Canadian Institutes of Health Research; Fundação para a Ciência e a Tecnologia; Genome Canada; Howard Hughes Medical Institute","keywords":"Epigenetics; DNA methylation; Genomic imprinting; Methylation; Biology; Imprinting (psychology); Genetics; Uniparental disomy; Epigenomics; Chromosome; Chromosome 7 (human); DNA; Gene; Karyotype; Gene expression","score_opus":0.015151807453028519,"score_gpt":0.2758209344289794,"score_spread":0.2606691269759509,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1974744326","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9994948,0.00008096007,0.0002343361,0.000006693751,7.6658677e-7,0.0000021453047,0.000037768852,0.0000069037637,0.00013555466],"genre_scores_gemma":[0.9993474,0.000063110805,0.00030729646,0.0000048277434,0.0000016931383,0.0000026451833,0.000105039966,0.000002689423,0.00016534502],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99969816,0.00007531377,0.000030498284,0.00008630042,0.00006754438,0.000042120555],"domain_scores_gemma":[0.9997378,0.000086804794,0.00007207745,0.000022954853,0.000030052397,0.000050238184],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.000404324,0.00027416984,0.00024101186,0.0005951072,0.00011725742,0.00023452504,0.00015514264,0.00017397541,0.00055483996],"category_scores_gemma":[0.00097373483,0.00018063893,0.000118820826,0.00025392653,0.00018208739,0.00011222179,0.00015333634,0.00017490036,0.0002036424],"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":[0.0008264467,0.00007501692,0.7217735,0.000022873326,0.000064906126,0.0020897617,0.0002587046,0.00033046107,0.2575015,0.00006333538,0.00009654932,0.01689697],"study_design_scores_gemma":[0.000020815973,0.0005783004,0.9217538,0.000004964714,0.00007741082,0.007602224,0.00010827146,0.0012530094,0.068012886,0.00003484311,0.00054449425,0.000008973079],"about_ca_topic_score_codex":0.001111412,"about_ca_topic_score_gemma":0.0015010408,"teacher_disagreement_score":0.001111412,"about_ca_system_score_codex":0.00016816636,"about_ca_system_score_gemma":0.000094428295,"threshold_uncertainty_score":0.0022098422},"labels":[],"label_agreement":null},{"id":"W1974960512","doi":"10.1016/j.fertnstert.2011.06.055","title":"Embryonic imprinting perturbations do not originate from superovulation-induced defects in DNA methylation acquisition","year":2011,"lang":"en","type":"article","venue":"Fertility and Sterility","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","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":"Children’s Health Research Institute; Western University","funders":"Ontario Ministry of Research and Innovation; Canadian Institutes of Health Research; Western University","keywords":"Imprinting (psychology); Oocyte; DNA methylation; Genomic imprinting; Biology; Andrology; Human fertilization; Blastocyst; Embryo; Methylation; Embryogenesis; Genetics; Gene; Medicine; Gene expression","score_opus":0.02988302671186601,"score_gpt":0.2533522563495421,"score_spread":0.2234692296376761,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1974960512","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.98706776,0.0014500294,0.0065763197,0.0001355049,0.00004657582,0.000038924834,0.0009953763,0.00024206634,0.003447449],"genre_scores_gemma":[0.9945815,0.0004559959,0.0013426836,0.000047249476,0.0000122837055,0.000034389646,0.0006226855,0.0000732414,0.0028298204],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99984705,0.000020998701,0.000017034385,0.000039409155,0.00004344278,0.000032054028],"domain_scores_gemma":[0.9994748,0.00013458022,0.00014900978,0.00011094174,0.00002459528,0.00010607964],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0001231576,0.0004934942,0.0003202592,0.0005472291,0.00012804188,0.00026242263,0.00042960045,0.00033598277,0.0031667824],"category_scores_gemma":[0.0003579405,0.00032967402,0.00025789722,0.00018233949,0.0005289228,0.00038469143,0.0006222937,0.0006901632,0.0005269897],"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":[0.00017779222,0.000009693715,0.0011084845,0.000019167454,0.000010791374,0.00025506323,0.000017414857,0.000051489344,0.9964228,0.00051686604,0.000030276875,0.0013800601],"study_design_scores_gemma":[0.000016022354,0.00011687851,0.021354325,0.0000055962323,0.000025951547,0.0015040367,0.000038088507,0.0005263028,0.9746661,0.00024177106,0.0014982466,0.0000066989755],"about_ca_topic_score_codex":0.0006642017,"about_ca_topic_score_gemma":0.0010348349,"teacher_disagreement_score":0.0031667824,"about_ca_system_score_codex":0.00026409782,"about_ca_system_score_gemma":0.00027266704,"threshold_uncertainty_score":0.01059401},"labels":[],"label_agreement":null},{"id":"W1975168528","doi":"10.1002/jbmr.408","title":"Exclusion of the <i>GNAS</i> locus in PHP-Ib patients with broad <i>GNAS</i> methylation changes: Evidence for an autosomal recessive form of PHP-Ib?","year":2011,"lang":"en","type":"article","venue":"Journal of Bone and Mineral Research","topic":"Genetic Syndromes and Imprinting","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":"University of Toronto; Mount Sinai Hospital","funders":"National Institute of Diabetes and Digestive and Kidney Diseases; Instituto de Salud Carlos III; National Institutes of Health","keywords":"GNAS complex locus; Locus (genetics); Genetics; Pseudohypoparathyroidism; Allele; Biology; Uniparental disomy; Genomic imprinting; Epigenetics; Copy-number variation; DNA methylation; Internal medicine; Medicine; Gene; Chromosome; Karyotype; Parathyroid hormone","score_opus":0.08765229711357614,"score_gpt":0.3486915315984225,"score_spread":0.26103923448484634,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1975168528","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9991731,0.000065104665,0.00009594393,0.000021307324,0.0000012907292,0.00000436174,0.000033372544,0.0000058001474,0.0005996607],"genre_scores_gemma":[0.9995541,0.00005042444,0.00017239047,0.000022981014,0.000004220786,0.000003433495,0.00007510942,0.000004365343,0.000113061185],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9998419,0.000015356203,0.00002204116,0.000056920384,0.000025556395,0.000038168793],"domain_scores_gemma":[0.99977046,0.00004534654,0.00006266691,0.000018037865,0.000022007618,0.00008147104],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00013928846,0.00043384693,0.00026744432,0.00056496164,0.00045345124,0.00034256978,0.00022886535,0.00042511232,0.0013905691],"category_scores_gemma":[0.00079136447,0.00022904066,0.00018889559,0.0003299045,0.00040939747,0.00021361241,0.00031197807,0.0003331012,0.00021965265],"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":[0.0006857267,0.000074223295,0.86225367,0.000056858633,0.000050300125,0.03128611,0.0010652824,0.00013056332,0.095123164,0.0001953188,0.00015137986,0.00892741],"study_design_scores_gemma":[0.000049267797,0.00045239637,0.8917428,0.000017126536,0.00007664726,0.09738507,0.00061108056,0.0004349168,0.0080882255,0.00014499696,0.0009830096,0.000014482068],"about_ca_topic_score_codex":0.0026764786,"about_ca_topic_score_gemma":0.0017457813,"teacher_disagreement_score":0.0026764786,"about_ca_system_score_codex":0.00021909564,"about_ca_system_score_gemma":0.00018345297,"threshold_uncertainty_score":0.0053218007},"labels":[],"label_agreement":null},{"id":"W1975445070","doi":"10.1007/s00431-008-0683-4","title":"Clinical and radiological findings in Schinzel–Giedion syndrome","year":2008,"lang":"en","type":"article","venue":"European Journal of Pediatrics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":23,"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":"Medicine; Radiological weapon; Radiology","score_opus":0.02433723706154628,"score_gpt":0.26046366487720896,"score_spread":0.23612642781566268,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1975445070","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.972119,0.0030610103,0.0010526464,0.0016714246,0.00014047723,0.00012782184,0.00066342734,0.00019184855,0.020972347],"genre_scores_gemma":[0.9971359,0.000828495,0.0006218325,0.00022166285,0.00016237861,0.00002173814,0.0001845354,0.000020654345,0.00080288504],"study_design_codex":"case_report","study_design_gemma":"case_report","domain_scores_codex":[0.99938416,0.00007574398,0.00008952886,0.00012538873,0.00013286588,0.0001923756],"domain_scores_gemma":[0.9976719,0.00090356235,0.00037800398,0.00010187966,0.00018318901,0.0007615564],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00042404662,0.0025159554,0.001020098,0.005187864,0.0008866455,0.000998942,0.0016780349,0.0035751315,0.0057679256],"category_scores_gemma":[0.004583979,0.0011965983,0.0006109396,0.0022996343,0.0030203664,0.0012050042,0.0012017161,0.0014959337,0.0010241396],"study_design_candidate":"case_report","study_design_consensus":"case_report","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0002284605,0.00005017793,0.01789342,0.000055889668,0.00002029662,0.97478354,0.00014684649,0.00019330865,0.0043387837,0.00028406756,0.0004564526,0.0015488175],"study_design_scores_gemma":[0.00009139021,0.00012220733,0.045502085,0.000025472222,0.00006647308,0.9506706,0.00019876126,0.00043319532,0.0018068233,0.0003834987,0.0006642483,0.000035300356],"about_ca_topic_score_codex":0.0068938807,"about_ca_topic_score_gemma":0.0033903264,"teacher_disagreement_score":0.0068938807,"about_ca_system_score_codex":0.0007691174,"about_ca_system_score_gemma":0.0012748502,"threshold_uncertainty_score":0.019295573},"labels":[],"label_agreement":null},{"id":"W1975501413","doi":"10.1159/000090847","title":"New chromosome 11p15 epigenotypes identified in male monozygotic twins with Beckwith-Wiedemann syndrome","year":2006,"lang":"en","type":"article","venue":"Cytogenetic and Genome Research","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":34,"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; University of Toronto","funders":"","keywords":"Beckwith–Wiedemann syndrome; Imprinting (psychology); Monozygotic twin; Genomic imprinting; Biology; Genetics; DNA methylation; Uniparental disomy; Methylation; Karyotype; Phenotype; Twin study; Chromosome; Gene; Heritability","score_opus":0.023737361495145076,"score_gpt":0.2839545408517143,"score_spread":0.2602171793565692,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1975501413","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99836487,0.0002152843,0.0005190841,0.000043658685,0.000022091537,0.00001334497,0.000082094266,0.0000128136635,0.00072664616],"genre_scores_gemma":[0.9989231,0.00012084479,0.00048129444,0.000030418107,0.000014762046,0.000007657266,0.0000727116,0.0000066192947,0.00034258034],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9994388,0.00008395595,0.000068665846,0.00015638061,0.00017670885,0.00007549549],"domain_scores_gemma":[0.99947804,0.00008686737,0.00020033136,0.000051293162,0.000042078966,0.0001415048],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00018541607,0.00045056848,0.0004715365,0.0014375801,0.0005439267,0.00038717684,0.00028292846,0.0005421844,0.0014144543],"category_scores_gemma":[0.0014222425,0.00038790243,0.0003288911,0.0004885824,0.0004409166,0.00014980153,0.00067463785,0.0003608387,0.00020401865],"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":[0.0013820162,0.00018604734,0.6300685,0.00012413735,0.0003080829,0.18285744,0.0025303487,0.00038637835,0.15055148,0.0013819517,0.00086970703,0.029354015],"study_design_scores_gemma":[0.000031017287,0.00043682562,0.62081605,0.000021831464,0.00012612274,0.36167926,0.00038722777,0.00058237807,0.014282648,0.00028994773,0.0013160077,0.000030741176],"about_ca_topic_score_codex":0.0012869849,"about_ca_topic_score_gemma":0.0017557213,"teacher_disagreement_score":0.0014375801,"about_ca_system_score_codex":0.00018470935,"about_ca_system_score_gemma":0.00014509395,"threshold_uncertainty_score":0.0047317743},"labels":[],"label_agreement":null},{"id":"W1975838349","doi":"10.1002/ajmg.a.33204","title":"Methylation profiling in individuals with Russell–Silver syndrome","year":2010,"lang":"en","type":"article","venue":"American Journal of Medical Genetics Part A","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":37,"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 Children's Hospital; Child and Family Research Institute; University of British Columbia","funders":"","keywords":"Methylation; CpG site; RSS; DNA methylation; Genomic imprinting; Biology; Differentially methylated regions; Epigenetics; Imprinting (psychology); Genetics; Bioinformatics; Gene; Gene expression; Computer science","score_opus":0.008323810880665215,"score_gpt":0.2683808778984834,"score_spread":0.2600570670178182,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1975838349","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99877435,0.0002602643,0.00024212383,0.000032076547,0.0000032902717,0.000005715702,0.00022807832,0.000023474393,0.00043048523],"genre_scores_gemma":[0.99916697,0.000101722115,0.00021462605,0.000030540417,0.000003778851,0.0000036135054,0.00016098804,0.000005597934,0.00031212278],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9997801,0.000031921074,0.000021265623,0.000091000096,0.000049796363,0.000025970865],"domain_scores_gemma":[0.99986064,0.00002930627,0.000044694483,0.000012471424,0.000026146676,0.000026790756],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00014746888,0.00034332994,0.00031671548,0.000892173,0.00025244293,0.00028684014,0.00014601565,0.00036425516,0.0011384853],"category_scores_gemma":[0.0005670505,0.00016191036,0.00017360307,0.00049971795,0.00016342606,0.00010124659,0.00022415355,0.00019389972,0.00019138548],"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":[0.000860385,0.00004747233,0.8264516,0.00005409007,0.00018491774,0.0039427285,0.0009328523,0.00032660348,0.14403035,0.000110642264,0.0005359802,0.022522258],"study_design_scores_gemma":[0.000015704072,0.0003865988,0.97626865,0.000010903464,0.00016820278,0.010634789,0.0003576174,0.00062647316,0.010033575,0.00015556585,0.0013257796,0.000016130605],"about_ca_topic_score_codex":0.0017119542,"about_ca_topic_score_gemma":0.002052452,"teacher_disagreement_score":0.0017119542,"about_ca_system_score_codex":0.00015934494,"about_ca_system_score_gemma":0.00006258152,"threshold_uncertainty_score":0.0038086176},"labels":[],"label_agreement":null},{"id":"W1976122890","doi":"10.1071/rdv27n1ab80","title":"80 DNA METHYLATION OF INSULIN-LIKE GROWTH FACTOR 2 (IGF2) GENE IN DAY 14 IN VITRO-PRODUCED BOVINE EMBRYOS OF DIFFERENT SIZES","year":2014,"lang":"en","type":"article","venue":"Reproduction Fertility and Development","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":0,"is_retracted":false,"has_abstract":true,"route_ca_aff":false,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":true,"ca_institutions":"","funders":"","keywords":"Biology; Embryo; Genomic imprinting; Andrology; Methylation; DNA methylation; Embryo culture; Pronucleus; Reprogramming; Bisulfite sequencing; Genetics; Embryogenesis; Gene; Molecular biology; Zygote; Gene expression","score_opus":0.014876506521756063,"score_gpt":0.23113201408733625,"score_spread":0.21625550756558018,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1976122890","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99484396,0.0009290955,0.0017472045,0.000021934497,0.000014285496,0.000013487071,0.00050247536,0.000014783986,0.0019128034],"genre_scores_gemma":[0.99156344,0.0005737132,0.0023971724,0.00003869384,0.0000043379846,0.000038215814,0.0015658189,0.000020701706,0.0037978943],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9998716,0.000016267657,0.00001221621,0.00004514762,0.00003234358,0.000022548516],"domain_scores_gemma":[0.99991226,0.000023492916,0.000020386216,0.000008619431,0.000017618117,0.00001761378],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.000112256464,0.00010300209,0.00016671937,0.000183992,0.00015880376,0.00019895613,0.0001002059,0.00015412761,0.00080234464],"category_scores_gemma":[0.00011787592,0.000107455875,0.00013528322,0.00011950214,0.00013181403,0.00006586131,0.00013589255,0.00018455372,0.00021020274],"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":[0.00006261938,0.0000048023367,0.00092037854,0.000010718707,0.0000024957856,0.000025060976,0.00003508387,0.000012992948,0.9983121,0.000010425262,0.000009482592,0.0005938525],"study_design_scores_gemma":[0.000013911355,0.0003360697,0.16190685,0.0000126730665,0.00003941913,0.00036936064,0.00014704373,0.0007615902,0.8330672,0.000033753422,0.0033026726,0.000009432556],"about_ca_topic_score_codex":0.0039216275,"about_ca_topic_score_gemma":0.0056316294,"teacher_disagreement_score":0.0039216275,"about_ca_system_score_codex":0.0002639123,"about_ca_system_score_gemma":0.00013296331,"threshold_uncertainty_score":0.007797599},"labels":[],"label_agreement":null},{"id":"W1976371489","doi":"10.1177/0883073812443591","title":"Angelman Syndrome Due to a Termination Codon Mutation of the <i>UBE3A</i> Gene","year":2012,"lang":"en","type":"article","venue":"Journal of Child Neurology","topic":"Genetic Syndromes and Imprinting","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":"University Health Network; Mount Sinai Hospital; SickKids Foundation; Hospital for Sick Children; University of Toronto","funders":"","keywords":"UBE3A; Angelman syndrome; Microcephaly; Genetics; Uniparental disomy; Imprinting (psychology); Biology; Phenotype; Intellectual disability; Speech delay; Ubiquitin ligase; Neurodevelopmental disorder; Gene; Mutation; Global developmental delay; Chromosome; Ubiquitin; Karyotype","score_opus":0.005556435576545026,"score_gpt":0.21905262722758612,"score_spread":0.21349619165104108,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1976371489","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9940526,0.0006272062,0.002165292,0.00018336382,0.00006503376,0.000021703725,0.00016623955,0.00018655538,0.0025319404],"genre_scores_gemma":[0.99740607,0.00037493164,0.0007674843,0.00007428813,0.00004161809,0.0000070901406,0.000110755514,0.000026730317,0.0011910594],"study_design_codex":"case_report","study_design_gemma":"case_report","domain_scores_codex":[0.99993145,0.000013097344,0.000007940154,0.000017413558,0.000013787113,0.000016188122],"domain_scores_gemma":[0.9997069,0.00007417402,0.00013229142,0.0000097961865,0.000010283306,0.000066522145],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00012034216,0.0010668886,0.00023967042,0.00028721202,0.00017823052,0.00016382031,0.00016166891,0.00038882412,0.001330268],"category_scores_gemma":[0.0006407468,0.00016761487,0.00022382702,0.00021939687,0.00047611177,0.00019028156,0.00024375822,0.00030714544,0.0004617753],"study_design_candidate":"case_report","study_design_consensus":"case_report","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00080214074,0.00011515822,0.0739864,0.00021486788,0.0001474719,0.71640027,0.0005435963,0.0008716727,0.18334533,0.0025681173,0.0015788815,0.01942605],"study_design_scores_gemma":[0.0002537732,0.00076444034,0.08694043,0.000054423428,0.00022189358,0.863252,0.00013810837,0.0015742581,0.03781181,0.0010859678,0.007859668,0.00004326436],"about_ca_topic_score_codex":0.0009540101,"about_ca_topic_score_gemma":0.0011798954,"teacher_disagreement_score":0.001330268,"about_ca_system_score_codex":0.00022996055,"about_ca_system_score_gemma":0.0002796761,"threshold_uncertainty_score":0.0044501424},"labels":[],"label_agreement":null},{"id":"W1977286970","doi":"10.1016/j.ydbio.2011.01.008","title":"Partial loss of Ascl2 function affects all three layers of the mature placenta and causes intrauterine growth restriction","year":2011,"lang":"en","type":"article","venue":"Developmental Biology","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":79,"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; University of British Columbia","keywords":"Biology; Trophoblast; Genetics; Genomic imprinting; Placentation; Allele; Placenta; Phenotype; Embryonic stem cell; Population; Cell biology; Gene; Fetus; Gene expression; Pregnancy; DNA methylation","score_opus":0.015555433931360569,"score_gpt":0.21395170461981253,"score_spread":0.19839627068845195,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1977286970","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9846437,0.0011287029,0.008270835,0.00036008484,0.0000862084,0.000030070136,0.0020538736,0.0006861361,0.002740412],"genre_scores_gemma":[0.99508625,0.00037410617,0.0013873674,0.00005936742,0.000023574943,0.000026321804,0.00062042056,0.00009819221,0.0023242773],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9997596,0.000040577404,0.000027745535,0.000053077583,0.000087409215,0.000031544503],"domain_scores_gemma":[0.9994618,0.0001199211,0.00016295648,0.00008149211,0.000019120702,0.00015467273],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00014338287,0.0012116042,0.00045385127,0.0011395871,0.0003437765,0.00046801168,0.0005496316,0.00063118956,0.002765161],"category_scores_gemma":[0.00032420797,0.00043556368,0.00042333012,0.0005220041,0.0013332411,0.00019742941,0.00073000684,0.00076826476,0.0005676992],"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":[0.00047241198,0.000036108264,0.0015774044,0.0000754761,0.00005456274,0.0056366683,0.00004865515,0.00087383384,0.986217,0.0007232568,0.00032524008,0.0039595007],"study_design_scores_gemma":[0.00011693339,0.00021012711,0.018325606,0.000013870269,0.00014399565,0.025738897,0.00008833333,0.0028567084,0.94564533,0.0004959227,0.006337996,0.000026368352],"about_ca_topic_score_codex":0.0010654913,"about_ca_topic_score_gemma":0.0010681466,"teacher_disagreement_score":0.002765161,"about_ca_system_score_codex":0.00043882255,"about_ca_system_score_gemma":0.00042183098,"threshold_uncertainty_score":0.009250343},"labels":[],"label_agreement":null},{"id":"W1977311839","doi":"10.1111/cge.12001","title":"<i>PIK3CA</i>, a hotspot for postzygotic mutations in nonhereditary overgrowth syndromes","year":2012,"lang":"en","type":"letter","venue":"Clinical Genetics","topic":"Genetic Syndromes and Imprinting","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":"Child and Family Research Institute; University of British Columbia","funders":"","keywords":"Citation; Library science; Genealogy; Columbia university; Genetics; History; Biology; Sociology; Computer science; Media studies","score_opus":0.05307838364426483,"score_gpt":0.3379449713470265,"score_spread":0.2848665877027617,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1977311839","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":[0.1123285,0.005149119,0.0017752624,0.81327885,0.031618852,0.00009329089,0.00044801988,0.00039743478,0.034910675],"genre_scores_gemma":[0.61666757,0.003816984,0.0022114713,0.25661182,0.09836177,0.00009382614,0.0002321658,0.00015500076,0.02184942],"study_design_codex":"case_report","study_design_gemma":"not_applicable","domain_scores_codex":[0.99948394,0.00010803255,0.0000730474,0.00009437021,0.00010911396,0.00013142376],"domain_scores_gemma":[0.9988809,0.0005515402,0.00012373339,0.000060081835,0.00015857755,0.00022508945],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0004462737,0.00094054453,0.000828136,0.000540148,0.0010760418,0.0010119935,0.000908519,0.01168966,0.0022317043],"category_scores_gemma":[0.0044350117,0.0003807458,0.0007938887,0.00045702155,0.0011341124,0.0009637907,0.00041222633,0.0054269894,0.0012724306],"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":[0.00055180845,0.000091692644,0.012965813,0.00014422224,0.000095464646,0.7012723,0.0002907546,0.00048273863,0.0045581134,0.0037056017,0.2583656,0.017475868],"study_design_scores_gemma":[0.0005593602,0.00034583147,0.01999986,0.00020378252,0.00028269866,0.8390765,0.00055578613,0.0055211033,0.0040782443,0.009331699,0.11992846,0.00011668323],"about_ca_topic_score_codex":0.0027279218,"about_ca_topic_score_gemma":0.002876311,"teacher_disagreement_score":0.01168966,"about_ca_system_score_codex":0.0016454534,"about_ca_system_score_gemma":0.00062630815,"threshold_uncertainty_score":0.011938691},"labels":[],"label_agreement":null},{"id":"W1977459685","doi":"10.1016/j.cub.2008.09.044","title":"Global Survey of Genomic Imprinting by Transcriptome Sequencing","year":2008,"lang":"en","type":"article","venue":"Current Biology","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":166,"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","funders":"","keywords":"Genomic imprinting; Biology; Imprinting (psychology); Genetics; Locus (genetics); Gene; Transcriptome; Genome; Allele; Computational biology; Gene expression; DNA methylation","score_opus":0.040187519973288406,"score_gpt":0.2898789089047664,"score_spread":0.24969138893147802,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1977459685","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.880977,0.002730774,0.09091645,0.00028095653,0.000070486,0.000058973408,0.01922915,0.0006043506,0.005131988],"genre_scores_gemma":[0.91684234,0.0025473717,0.0465277,0.0003536891,0.00006854909,0.0001335334,0.028876843,0.0003145593,0.0043353974],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.99983215,0.000020460639,0.0000067423966,0.000074967415,0.00003893014,0.000026636859],"domain_scores_gemma":[0.99971884,0.00007407304,0.000044487737,0.000058741065,0.000049116894,0.00005475917],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00028322102,0.00034323309,0.0005090248,0.00056495355,0.00029121176,0.00063012453,0.00020437397,0.00023997886,0.0009343085],"category_scores_gemma":[0.000273824,0.00017561157,0.0004241287,0.0007881802,0.0002667501,0.0002886004,0.00039720006,0.0007212232,0.0004337553],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.000089185836,0.000008029283,0.0027771362,0.000035808716,0.000038004317,0.000023399807,0.00002715489,0.00024008841,0.99078345,0.00017187596,0.00013280608,0.005673016],"study_design_scores_gemma":[0.000043126336,0.0003450849,0.35537145,0.000025806441,0.00037169037,0.0006878431,0.00028662998,0.008342367,0.61423165,0.0020690674,0.01818637,0.00003898173],"about_ca_topic_score_codex":0.0010630095,"about_ca_topic_score_gemma":0.0023260522,"teacher_disagreement_score":0.0010630095,"about_ca_system_score_codex":0.00022707628,"about_ca_system_score_gemma":0.00033684922,"threshold_uncertainty_score":0.0031255484},"labels":[],"label_agreement":null},{"id":"W1977520107","doi":"10.1371/journal.pgen.1003752","title":"Stochastic Loss of Silencing of the Imprinted Ndn/NDN Allele, in a Mouse Model and Humans with Prader-Willi Syndrome, Has Functional Consequences","year":2013,"lang":"en","type":"article","venue":"PLoS Genetics","topic":"Genetic Syndromes and Imprinting","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":"University of Alberta","funders":"Canadian Institutes of Health Research; Institut National de la Santé et de la Recherche Médicale; Agence Nationale de la Recherche","keywords":"Allele; Genomic imprinting; Biology; Imprinting (psychology); Genetics; Context (archaeology); Epigenetics; Allelic exclusion; Gene silencing; Gene; Gene expression; DNA methylation","score_opus":0.02239412840058208,"score_gpt":0.20857546569764904,"score_spread":0.18618133729706696,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1977520107","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9636065,0.0031366856,0.028613543,0.00028441165,0.00009640677,0.00007376911,0.0013061623,0.00045186476,0.0024306392],"genre_scores_gemma":[0.97918576,0.0019888515,0.009539129,0.00012814689,0.000020417974,0.0001364724,0.001020911,0.000096965676,0.007883382],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.99969685,0.000026453627,0.00002173295,0.00012753384,0.00010089739,0.00002652226],"domain_scores_gemma":[0.9998118,0.000020666565,0.00008788992,0.000029237592,0.000010878545,0.000039617087],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00012554228,0.0005628212,0.00023906401,0.0007327739,0.00015139188,0.00029023612,0.000329488,0.0005000071,0.0025480483],"category_scores_gemma":[0.00017408727,0.00028029623,0.0003898368,0.00022596357,0.00055936,0.00027457793,0.00040761256,0.0008818175,0.00043178562],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.000075653326,0.000031961157,0.00085924484,0.000043523258,0.000015958383,0.00019196312,0.00001760764,0.000069084774,0.9964541,0.00028569432,0.000051804516,0.0019033578],"study_design_scores_gemma":[0.00003731483,0.0005581721,0.03197638,0.000030278874,0.00010555292,0.004545194,0.00006488029,0.0019377705,0.9538806,0.0005813841,0.006261419,0.00002115361],"about_ca_topic_score_codex":0.00059455587,"about_ca_topic_score_gemma":0.0016545138,"teacher_disagreement_score":0.0025480483,"about_ca_system_score_codex":0.00027341678,"about_ca_system_score_gemma":0.00019224767,"threshold_uncertainty_score":0.00852406},"labels":[],"label_agreement":null},{"id":"W1977614198","doi":"10.1111/j.1432-0436.2008.00281.x","title":"The Prader–Willi syndrome protein necdin interacts with the E1A-like inhibitor of differentiation EID-1 and promotes myoblast differentiation","year":2008,"lang":"en","type":"article","venue":"Differentiation","topic":"Genetic Syndromes and Imprinting","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":"University of Alberta","funders":"Eunice Kennedy Shriver National Institute of Child Health and Human Development","keywords":"Myogenesis; MyoD; Myocyte; Biology; Cellular differentiation; Embryonic stem cell; Cell biology; Transactivation; Cytoplasm; Myosin; Myotome; Molecular biology; Gene; Biochemistry; Gene expression","score_opus":0.00711462439299974,"score_gpt":0.1967704049808753,"score_spread":0.18965578058787558,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1977614198","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99223596,0.0025912076,0.0022828726,0.00020093207,0.000038344384,0.000008777808,0.00015132817,0.000041429103,0.002449236],"genre_scores_gemma":[0.992238,0.00081184757,0.0020835956,0.00008487343,0.000008565636,0.000011884725,0.0005832981,0.000024191208,0.004153727],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99983525,0.000033592416,0.000012233476,0.000036515274,0.000045978704,0.00003630893],"domain_scores_gemma":[0.9998827,0.000020477073,0.00003350465,0.000016067459,0.000010585916,0.00003668056],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00013623442,0.0002916627,0.00022746631,0.00028106477,0.00032627775,0.0003877067,0.00032980385,0.00029365715,0.0014366193],"category_scores_gemma":[0.00027639573,0.0002907019,0.00022802394,0.00018254788,0.00027340947,0.00027966572,0.0005728509,0.00054699444,0.0010109305],"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":[0.00008356719,0.000008759933,0.00095818844,0.000017811106,0.000008237565,0.00027158912,0.000012490573,0.00012422698,0.9973719,0.00023363753,0.000078224,0.00083131954],"study_design_scores_gemma":[0.000032672197,0.00007203849,0.03298017,0.000011241419,0.000020525642,0.0019159135,0.00007298072,0.0034444914,0.95489407,0.00017185697,0.006374686,0.000009395558],"about_ca_topic_score_codex":0.00091548904,"about_ca_topic_score_gemma":0.0016906464,"teacher_disagreement_score":0.0014366193,"about_ca_system_score_codex":0.000678153,"about_ca_system_score_gemma":0.00017206042,"threshold_uncertainty_score":0.0049203634},"labels":[],"label_agreement":null},{"id":"W1978634652","doi":"10.1111/j.1399-0004.2009.01171_3.x","title":"<i>ZFP57 </i>mutations cause an autosomal recessive imprinting disorder","year":2009,"lang":"en","type":"article","venue":"Clinical Genetics","topic":"Genetic Syndromes and Imprinting","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":"University of British Columbia","funders":"","keywords":"Imprinting (psychology); Genetics; Biology; Genomic imprinting; Mutation; DNA methylation; Gene; Gene expression","score_opus":0.03435661318581114,"score_gpt":0.3623240367160443,"score_spread":0.32796742353023317,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1978634652","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9940216,0.00067319657,0.0014588244,0.0004236503,0.000056371537,0.000024047979,0.00042497148,0.00018076933,0.00273656],"genre_scores_gemma":[0.9979456,0.00018885193,0.0009239826,0.000101622194,0.00004096552,0.0000061421474,0.00011505149,0.000030099567,0.0006477966],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.99981064,0.000015339521,0.00002359538,0.0000618115,0.000057202116,0.000031442643],"domain_scores_gemma":[0.9996817,0.00006739271,0.00012844172,0.000014067772,0.000016803728,0.00009154471],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00015033758,0.001269139,0.00037760157,0.0007393196,0.00044716685,0.0003015639,0.00044232368,0.0006518081,0.0024501395],"category_scores_gemma":[0.00052688975,0.000251708,0.00029338486,0.00038297422,0.00072923186,0.00015879633,0.0005080553,0.00043227675,0.00042044595],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0016129223,0.0001455753,0.07723041,0.0001920048,0.00029901153,0.31243777,0.00052737887,0.0005994702,0.5803822,0.0020621733,0.003968214,0.020542765],"study_design_scores_gemma":[0.00031134184,0.00047210377,0.3475716,0.00009642671,0.0005025286,0.5577101,0.00028612252,0.0012622603,0.08495186,0.0010661642,0.005701011,0.0000683968],"about_ca_topic_score_codex":0.0023297311,"about_ca_topic_score_gemma":0.002161469,"teacher_disagreement_score":0.0024501395,"about_ca_system_score_codex":0.00033897604,"about_ca_system_score_gemma":0.00024039543,"threshold_uncertainty_score":0.008196533},"labels":[],"label_agreement":null},{"id":"W1979477332","doi":"10.1016/j.placenta.2011.12.009","title":"TMED2/p24β1 is expressed in all gestational stages of human placentas and in choriocarcinoma cell lines","year":2011,"lang":"en","type":"article","venue":"Placenta","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","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":"Montreal Children's Hospital; McGill University Health Centre; McGill University","funders":"Canadian Institutes of Health Research","keywords":"Cytotrophoblast; Syncytiotrophoblast; Golgi apparatus; Endoplasmic reticulum; Cell biology; Placenta; Choriocarcinoma; Biology; Fetus; Genetics; Pregnancy","score_opus":0.03274435760820587,"score_gpt":0.26311413368400566,"score_spread":0.23036977607579978,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1979477332","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.98492557,0.0036561068,0.005334006,0.00013747913,0.00003572542,0.000027836391,0.0025799791,0.0001548369,0.0031485062],"genre_scores_gemma":[0.9879973,0.0012693632,0.0018519586,0.00003717355,0.000011202709,0.000036794045,0.003922451,0.000049398324,0.0048243064],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9998549,0.00001327827,0.000015815758,0.00003768009,0.000034996927,0.000043152468],"domain_scores_gemma":[0.99981874,0.000027953572,0.000035008477,0.000038905782,0.00003199613,0.00004746858],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.000176671,0.00030383887,0.0002153285,0.00076777366,0.00030676235,0.0007560736,0.00025923311,0.00020012277,0.0013743776],"category_scores_gemma":[0.00033042667,0.0002775357,0.00023959044,0.0005090951,0.00027511382,0.00028290015,0.0003510828,0.0003912991,0.00043638097],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00017951267,0.000010464048,0.0020773644,0.000030987278,0.000013427445,0.00043973103,0.000111323956,0.00004183843,0.9955776,0.00017452959,0.000060778497,0.0012823896],"study_design_scores_gemma":[0.00001715073,0.00010318948,0.04465784,0.000011549032,0.000039301944,0.0034245015,0.00030218696,0.00037698305,0.93871903,0.00018272594,0.012153492,0.000012074448],"about_ca_topic_score_codex":0.0020770768,"about_ca_topic_score_gemma":0.0013432782,"teacher_disagreement_score":0.0020770768,"about_ca_system_score_codex":0.0003509784,"about_ca_system_score_gemma":0.00025305888,"threshold_uncertainty_score":0.0045977235},"labels":[],"label_agreement":null},{"id":"W1979892065","doi":"10.1016/j.cell.2011.12.035","title":"Base-Resolution Analyses of Sequence and Parent-of-Origin Dependent DNA Methylation in the Mouse Genome","year":2012,"lang":"en","type":"article","venue":"Cell","topic":"Genetic Syndromes and Imprinting","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 Health Network; Hospital for Sick Children","funders":"National Institute of Environmental Health Sciences; National Human Genome Research Institute","keywords":"Biology; Genomic imprinting; DNA methylation; Differentially methylated regions; Imprinting (psychology); Epigenetics; Genetics; Methylation; CpG site; Genome; RNA-Directed DNA Methylation; Illumina Methylation Assay; Gene; Gene expression","score_opus":0.060456148872561954,"score_gpt":0.3116637991607433,"score_spread":0.25120765028818137,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1979892065","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9912902,0.0015759055,0.0050124917,0.00006582716,0.0000101891865,0.000008862673,0.0005926007,0.000085935,0.0013579702],"genre_scores_gemma":[0.98997736,0.0009549521,0.005558191,0.000047018148,0.000007423568,0.000013330768,0.0013054265,0.00006614258,0.0020700549],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9998957,0.000017928542,0.0000068645595,0.000028843879,0.00003236544,0.00001824613],"domain_scores_gemma":[0.9996506,0.000120764525,0.00009471669,0.00004977054,0.00003840076,0.000045781384],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00022517533,0.00021453745,0.00017827182,0.0006001553,0.00022935183,0.00022756633,0.000353584,0.00031239388,0.0012634456],"category_scores_gemma":[0.0003991543,0.00028025106,0.00021781384,0.00038308336,0.00024015672,0.00014998464,0.00020711249,0.0006673319,0.00037009947],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.000086107175,0.0000052384794,0.0006613246,0.000017542601,0.000008844753,0.00002338069,0.000025411273,0.00007885304,0.9978041,0.00018740664,0.000014306238,0.0010874685],"study_design_scores_gemma":[0.00001755258,0.00013359217,0.05272349,0.0000069633816,0.00007767003,0.00046992567,0.00004825977,0.000948453,0.9430577,0.0003125291,0.002193623,0.0000102286585],"about_ca_topic_score_codex":0.0016143827,"about_ca_topic_score_gemma":0.0047824797,"teacher_disagreement_score":0.0016143827,"about_ca_system_score_codex":0.00019235218,"about_ca_system_score_gemma":0.00014347052,"threshold_uncertainty_score":0.004226625},"labels":[],"label_agreement":null},{"id":"W1980941373","doi":"10.1086/508500","title":"Epigenetic Allele Silencing Unveils Recessive RYR1 Mutations in Core Myopathies","year":2006,"lang":"en","type":"article","venue":"The American Journal of Human Genetics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":135,"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. Thomas Hospital","funders":"","keywords":"RYR1; Genetics; Epigenetics; Allele; Gene silencing; Biology; Gene","score_opus":0.01334378897392324,"score_gpt":0.2715675876359422,"score_spread":0.25822379866201894,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1980941373","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9932488,0.0005924342,0.0029657974,0.0002057017,0.00003825161,0.000007713714,0.00014018263,0.00024989684,0.0025513028],"genre_scores_gemma":[0.99800676,0.00019682382,0.00069565664,0.000041673546,0.000016634489,0.000004051768,0.000050027622,0.00006247987,0.0009258669],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9998031,0.000035848716,0.000023581953,0.00003497903,0.0000653184,0.000037178143],"domain_scores_gemma":[0.9997496,0.00009336213,0.00006119201,0.000037409598,0.000015056435,0.00004344882],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00021713536,0.00050422415,0.00043921612,0.00051876414,0.00017370688,0.00031831348,0.0003531703,0.0005304372,0.0020573745],"category_scores_gemma":[0.0005777048,0.00022583046,0.00020868343,0.00019670224,0.00050983863,0.00022369027,0.0006246096,0.00043873972,0.00044949728],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0003115936,0.000019913965,0.0025906414,0.000037464637,0.000026041262,0.0063247206,0.00006857563,0.00036826124,0.98070866,0.0013545663,0.00022956503,0.007959919],"study_design_scores_gemma":[0.00016838494,0.00051059347,0.07140385,0.000024863677,0.0002576411,0.06750349,0.00020926648,0.006140553,0.84381586,0.0024633934,0.007446889,0.000055245077],"about_ca_topic_score_codex":0.0002882064,"about_ca_topic_score_gemma":0.00066077296,"teacher_disagreement_score":0.0020573745,"about_ca_system_score_codex":0.0001566546,"about_ca_system_score_gemma":0.00013331826,"threshold_uncertainty_score":0.006882608},"labels":[],"label_agreement":null},{"id":"W1981005523","doi":"10.4161/epi.21495","title":"A genome-wide approach reveals novel imprinted genes expressed in the human placenta","year":2012,"lang":"en","type":"article","venue":"Epigenetics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":94,"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 Nautical Research Society","funders":"Fondation pour la Recherche Médicale","keywords":"Genomic imprinting; Biology; Gene; Genetics; Human genome; Genome; Candidate gene; Single-nucleotide polymorphism; DNA microarray; Imprinting (psychology); Computational biology; Gene expression; DNA methylation; Genotype","score_opus":0.027120757413477622,"score_gpt":0.26441057039743643,"score_spread":0.2372898129839588,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1981005523","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.98757786,0.0017314693,0.0067282044,0.000072777264,0.000008360319,0.000029345536,0.003187499,0.0001213882,0.0005430502],"genre_scores_gemma":[0.98837984,0.000625527,0.006478791,0.00007904315,0.000012492031,0.000026712005,0.0038797972,0.00002612315,0.00049167953],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.99981254,0.000023295146,0.000009282124,0.00010012388,0.000026744643,0.000028087949],"domain_scores_gemma":[0.9998728,0.00006323883,0.000020563799,0.000014610258,0.000012859345,0.000015885214],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00021861884,0.00020286333,0.00036666417,0.0008710482,0.00022168677,0.00036015426,0.0001686407,0.00024081685,0.0013320042],"category_scores_gemma":[0.00035910067,0.00016426468,0.00047724255,0.000820577,0.000107801025,0.00008787326,0.00025200404,0.00029886974,0.00031061436],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0014385335,0.00007915504,0.14014982,0.00028452624,0.000533023,0.0014305254,0.00021853989,0.0010988814,0.8148022,0.00016351546,0.00062915095,0.039172165],"study_design_scores_gemma":[0.000043066622,0.00030469647,0.9359692,0.000014349251,0.00044111136,0.0033389733,0.00012062562,0.0036727937,0.052127037,0.00021708968,0.0037315476,0.000019482308],"about_ca_topic_score_codex":0.0010808454,"about_ca_topic_score_gemma":0.0014031397,"teacher_disagreement_score":0.0013320042,"about_ca_system_score_codex":0.000099433935,"about_ca_system_score_gemma":0.00015657036,"threshold_uncertainty_score":0.0044560432},"labels":[],"label_agreement":null},{"id":"W1981086785","doi":"10.1086/303072","title":"Multipoint Genetic Mapping with Uniparental Disomy Data","year":2000,"lang":"en","type":"article","venue":"The American Journal of Human Genetics","topic":"Genetic Syndromes and Imprinting","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 British Columbia","funders":"Eunice Kennedy Shriver National Institute of Child Health and Human Development; National Institute of General Medical Sciences; National Institutes of Health; March of Dimes Foundation","keywords":"Crossover; Uniparental disomy; Nondisjunction; International HapMap Project; Genetics; Chromosome; Computer science; Genetic algorithm; Set (abstract data type); Computational biology; Data mining; Biology; Algorithm; Artificial intelligence; Machine learning; Single-nucleotide polymorphism; Aneuploidy; Genotype; Gene; Karyotype","score_opus":0.02058943391585121,"score_gpt":0.26395974785119264,"score_spread":0.24337031393534142,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1981086785","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.7480456,0.0042454153,0.22159632,0.0004977792,0.000313196,0.00020873603,0.0050511905,0.0010417117,0.01899999],"genre_scores_gemma":[0.881186,0.0011477578,0.10901374,0.000106555286,0.00010841449,0.00018383995,0.003152942,0.00015419287,0.004946443],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99894947,0.00032917966,0.00011891201,0.00030342117,0.00023219024,0.00006680462],"domain_scores_gemma":[0.99744177,0.0011140235,0.00041938908,0.0006997404,0.0001407568,0.0001843538],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0013258435,0.00057727436,0.00078013365,0.0049927053,0.00072120014,0.0005878525,0.00092591223,0.00041939874,0.006409136],"category_scores_gemma":[0.002345049,0.0005238993,0.0006788484,0.0025254367,0.00045606607,0.00049831707,0.0009243209,0.0007681311,0.001641472],"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":[0.0022478064,0.00019093655,0.025275052,0.00049853476,0.00038746308,0.0043151774,0.0005345698,0.0025540479,0.85360706,0.017873818,0.0017051635,0.09081037],"study_design_scores_gemma":[0.00041628283,0.0011012224,0.19950375,0.00018103853,0.0010831001,0.03135506,0.00034585746,0.012778853,0.6412865,0.04143896,0.070308805,0.0002006178],"about_ca_topic_score_codex":0.00077199657,"about_ca_topic_score_gemma":0.0015385111,"teacher_disagreement_score":0.006409136,"about_ca_system_score_codex":0.00040782048,"about_ca_system_score_gemma":0.00018512228,"threshold_uncertainty_score":0.021440685},"labels":[],"label_agreement":null},{"id":"W1981409564","doi":"10.1007/s10803-006-0225-8","title":"Characterization of an Autism-Associated Segmental Maternal Heterodisomy of the Chromosome 15q11–13 Region","year":2006,"lang":"en","type":"article","venue":"Journal of Autism and Developmental Disorders","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":30,"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 of Toronto; York University","funders":"Canadian Institutes of Health Research; Sick Kids Foundation; Genome Canada; Howard Hughes Medical Institute","keywords":"Autism; Angelman syndrome; Genetics; Locus (genetics); Gene duplication; Developmental disorder; Fluorescence in situ hybridization; Psychology; Copy-number variation; Chromosome 15; Linkage disequilibrium; Biology; Heritability of autism; Chromosome; Gene; Autism spectrum disorder; Developmental psychology; Genotype; Single-nucleotide polymorphism; Genome","score_opus":0.004208866993457113,"score_gpt":0.19112138704434414,"score_spread":0.18691252005088704,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1981409564","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9950236,0.0005398812,0.002666813,0.00008113906,0.000018516117,0.000019638892,0.00030767662,0.000035191042,0.0013075239],"genre_scores_gemma":[0.99797076,0.00014317069,0.0011435762,0.000025084873,0.0000059768977,0.000009422037,0.00026125155,0.0000065876548,0.00043414987],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.99989116,0.000013241698,0.000011753443,0.000040737927,0.000021688058,0.000021350514],"domain_scores_gemma":[0.9996966,0.00012879544,0.000069176655,0.000028119532,0.000019890429,0.00005744256],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00010906412,0.00024136876,0.00030244008,0.00073367846,0.00020923512,0.00018603748,0.0003182052,0.00032937527,0.0026047407],"category_scores_gemma":[0.00045539162,0.00019353435,0.00026647002,0.00027190562,0.0002863232,0.00009695505,0.00037774828,0.00034396403,0.00028687378],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00041226114,0.00004435231,0.013181906,0.00006840022,0.000071825976,0.0072201067,0.00013879509,0.0002362315,0.97180194,0.00051750324,0.000100135425,0.0062064664],"study_design_scores_gemma":[0.000143123,0.0007759146,0.47144374,0.000037819762,0.00033253868,0.05387199,0.0003379626,0.002319078,0.46423337,0.00071725884,0.0057575,0.000029608567],"about_ca_topic_score_codex":0.0010693881,"about_ca_topic_score_gemma":0.0016116144,"teacher_disagreement_score":0.0026047407,"about_ca_system_score_codex":0.00020630856,"about_ca_system_score_gemma":0.00015501681,"threshold_uncertainty_score":0.008713782},"labels":[],"label_agreement":null},{"id":"W1983185429","doi":"10.1002/ajmg.a.36845","title":"A population‐based profile of 160 Australians with Prader‐Willi syndrome: Trends in diagnosis, birth prevalence and birth characteristics","year":2014,"lang":"en","type":"article","venue":"American Journal of Medical Genetics Part A","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":100,"is_retracted":false,"has_abstract":true,"route_ca_aff":false,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":true,"ca_institutions":"","funders":"State Government of Victoria","keywords":"Medicine; Gestational age; Uniparental disomy; Birth weight; Gestation; Population; Pediatrics; Epidemiology; Quarter (Canadian coin); Pregnancy; Obstetrics; Internal medicine; Biology; Genetics","score_opus":0.009621312756666363,"score_gpt":0.26305490539451176,"score_spread":0.2534335926378454,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1983185429","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9990901,0.000103704595,0.00007140561,0.00004102474,0.0000013712511,0.000015580965,0.00039581434,0.0000028122163,0.0002780487],"genre_scores_gemma":[0.99843985,0.0003328148,0.0002260109,0.000052429343,0.000003828596,0.000036188132,0.0005948629,0.0000018215869,0.00031222714],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9993906,0.00012967752,0.00009401458,0.0001293089,0.00017990863,0.00007648216],"domain_scores_gemma":[0.998607,0.00019400542,0.0004982935,0.00009194755,0.00038257006,0.00022616066],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0008813131,0.00015372325,0.00029943645,0.001721618,0.00064265827,0.0005470547,0.00045571473,0.0004130644,0.0009004132],"category_scores_gemma":[0.002591852,0.0004616705,0.00027958068,0.002403317,0.00043991863,0.0006924424,0.00096896966,0.00043230125,0.00027088512],"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":[0.000018904066,0.000022198747,0.99673283,0.000028300474,0.000015601769,0.00008865732,0.0008931612,0.000041358417,0.00034979466,0.000021344744,0.000091667745,0.0016962457],"study_design_scores_gemma":[9.040175e-7,0.00003621915,0.9992755,0.0000053508447,0.000004250994,0.00012666041,0.00035311215,0.000082162325,0.000014441233,0.0000109355615,0.00008818405,0.000002339239],"about_ca_topic_score_codex":0.11727906,"about_ca_topic_score_gemma":0.104870796,"teacher_disagreement_score":0.11727906,"about_ca_system_score_codex":0.0010757651,"about_ca_system_score_gemma":0.0007020058,"threshold_uncertainty_score":0.2331928},"labels":[],"label_agreement":null},{"id":"W1983528383","doi":"10.1002/ajmg.10702","title":"Evidence for imprinting on chromosome 16: The effect of uniparental disomy on the outcome of mosaic trisomy 16 pregnancies","year":2002,"lang":"en","type":"article","venue":"American Journal of Medical Genetics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":114,"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":"Canadian Institutes of Health Research; Killam Trusts","keywords":"Uniparental disomy; Genomic imprinting; Trisomy; Imprinting (psychology); Biology; Genetics; Chromosome 15; Intrauterine growth restriction; Aneuploidy; Chromosome; Fetus; Pregnancy; Karyotype; Gene; Gene expression","score_opus":0.03753954184212826,"score_gpt":0.3112880723604011,"score_spread":0.27374853051827286,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1983528383","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9967354,0.0018582684,0.00046511836,0.0001345044,0.000014066967,0.000005240635,0.00018342315,0.000016553453,0.0005874869],"genre_scores_gemma":[0.99936444,0.00023522573,0.00015363656,0.000017525637,0.000018002638,0.000004153931,0.000078439654,0.000007776812,0.00012083166],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99722075,0.0014575135,0.00017452263,0.0005356888,0.00037361355,0.00023786945],"domain_scores_gemma":[0.9787052,0.010739694,0.0067376937,0.0015874177,0.00028262785,0.0019473741],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0036583391,0.00061358826,0.0006695294,0.0011241045,0.00020472698,0.00052681746,0.00076053,0.00073653104,0.0029304314],"category_scores_gemma":[0.010809527,0.00024689932,0.0009356474,0.00074449816,0.0010935185,0.0003791519,0.0007674496,0.0008527677,0.00028040554],"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":[0.0031485618,0.000059745325,0.9851421,0.00006355462,0.0007953916,0.00078791095,0.000059129798,0.00020737962,0.004761387,0.000055685265,0.000063812484,0.004855491],"study_design_scores_gemma":[0.000025958549,0.00086438726,0.99534273,0.000018556428,0.00033273778,0.0019065276,0.000038338832,0.0005395601,0.00068437663,0.00013184837,0.00010564934,0.00000937464],"about_ca_topic_score_codex":0.0007743904,"about_ca_topic_score_gemma":0.0006157057,"teacher_disagreement_score":0.0036583391,"about_ca_system_score_codex":0.00021131238,"about_ca_system_score_gemma":0.0003587144,"threshold_uncertainty_score":0.01934737},"labels":[],"label_agreement":null},{"id":"W1983611341","doi":"10.1002/ajmg.a.35704","title":"Special section. Syndrome‐specific growth charts","year":2012,"lang":"en","type":"article","venue":"American Journal of Medical Genetics Part A","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":11,"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 Children's Hospital; Children's Hospital of Eastern Ontario; University of British Columbia","funders":"Barth Syndrome Foundation","keywords":"Geneticist; Terminology; Identification (biology); Normative; Disease; Medical genetics; Psychology; Medicine; Biology; Genetics; Pathology; Political science","score_opus":0.011881965174896172,"score_gpt":0.25256468583822755,"score_spread":0.24068272066333138,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1983611341","genre_codex":"other","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":[0.0051536136,0.05058388,0.023199422,0.088457935,0.26199073,0.0020159911,0.054094464,0.02025784,0.49424613],"genre_scores_gemma":[0.020335333,0.072868936,0.04742145,0.054897994,0.17652683,0.0032765586,0.08831913,0.007476052,0.5288777],"study_design_codex":"not_applicable","study_design_gemma":"not_applicable","domain_scores_codex":[0.99875426,0.00019765018,0.0002474452,0.0001035806,0.0005978762,0.000099117824],"domain_scores_gemma":[0.99222785,0.0023805269,0.0008174988,0.00041502452,0.0030662448,0.0010928415],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0012882819,0.0012738543,0.001183335,0.0045616664,0.0005556896,0.0020924113,0.0011967329,0.0019276564,0.16063385],"category_scores_gemma":[0.012865304,0.00045486906,0.0005224339,0.0026414406,0.00032440678,0.0020724435,0.0017021211,0.00264107,0.08173187],"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":[0.000011063161,0.000020222136,0.00024733017,0.000061984334,0.0000013279066,0.00008555444,0.000015529798,0.00004578291,0.00006537847,0.0003922667,0.9455036,0.053549998],"study_design_scores_gemma":[0.000012282568,0.000021963364,0.0015437207,0.00024594675,0.0000023321168,0.0010627123,0.000033304415,0.00008163657,0.00008262504,0.00087336334,0.99602795,0.00001230414],"about_ca_topic_score_codex":0.0015698428,"about_ca_topic_score_gemma":0.002737925,"teacher_disagreement_score":0.16063385,"about_ca_system_score_codex":0.00062388193,"about_ca_system_score_gemma":0.0014533895,"threshold_uncertainty_score":0.5373738},"labels":[],"label_agreement":null},{"id":"W1983877345","doi":"10.4021/jocmr2009.04.1234","title":"Schatzki’s Ring in Angelman Syndrome: A Diagnostic Dilemma in Neurodevelopmentally Disabled Patients","year":2009,"lang":"en","type":"article","venue":"Journal of Clinical Medicine Research","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":0,"is_retracted":false,"has_abstract":true,"route_ca_aff":false,"route_ca_fund":false,"route_ca_venue":true,"route_about_ca":false,"ca_institutions":"","funders":"U.S. Department of Defense","keywords":"Angelman syndrome; Medicine; Epilepsy; Cognition; Pediatrics; Psychiatry; Genetics","score_opus":0.085706213401256,"score_gpt":0.44808550450900464,"score_spread":0.36237929110774864,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1983877345","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9653738,0.00826749,0.0030591423,0.01363907,0.00027729743,0.00010670843,0.00017757123,0.00017528501,0.00892365],"genre_scores_gemma":[0.99306995,0.0021690316,0.0025089947,0.001173943,0.00051431445,0.000023310047,0.000057613695,0.000017354669,0.000465511],"study_design_codex":"case_report","study_design_gemma":"case_report","domain_scores_codex":[0.99968183,0.00007447176,0.00006589821,0.00004094649,0.000058558453,0.00007834523],"domain_scores_gemma":[0.99838936,0.00086956116,0.00026199277,0.000040772557,0.000120543395,0.00031774948],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0009383148,0.00070610474,0.00058238994,0.0010583582,0.000730715,0.0008328342,0.00084219,0.0024973203,0.0020143834],"category_scores_gemma":[0.006405244,0.00023463798,0.00015541789,0.0005150661,0.0011663102,0.0013117727,0.0006288916,0.0011416826,0.00073559384],"study_design_candidate":"case_report","study_design_consensus":"case_report","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0003303892,0.000058880974,0.1706559,0.00013962649,0.000013939996,0.79137117,0.00086464535,0.00030753834,0.004503262,0.0009551088,0.0039446233,0.026854998],"study_design_scores_gemma":[0.000034250534,0.00012501684,0.025059376,0.00010807025,0.00002144904,0.96662605,0.0014543413,0.0009905024,0.0015512257,0.0014309891,0.002576811,0.000021899048],"about_ca_topic_score_codex":0.0010210128,"about_ca_topic_score_gemma":0.0010757083,"teacher_disagreement_score":0.0024973203,"about_ca_system_score_codex":0.00039606908,"about_ca_system_score_gemma":0.00056379894,"threshold_uncertainty_score":0.0067387223},"labels":[],"label_agreement":null},{"id":"W1984422705","doi":"10.1186/1297-9686-39-5-599","title":"NNAT and DIRAS3 genes are paternally expressed in pigs","year":2007,"lang":"en","type":"article","venue":"Genetics Selection Evolution","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":22,"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 Natural Science Foundation of China","keywords":"Biology; Genomic imprinting; Epigenetics; Gene; Genetics; Imprinting (psychology); Gene expression; DNA methylation","score_opus":0.00777835974045534,"score_gpt":0.22748769520441509,"score_spread":0.21970933546395974,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1984422705","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9989497,0.00014981143,0.0004234886,0.000012398328,0.000003673218,0.0000012160408,0.00006484339,0.0000063035195,0.00038852327],"genre_scores_gemma":[0.9981305,0.00015314219,0.00055277284,0.000024723748,0.000004951011,0.0000046013274,0.00021196519,0.000008280391,0.0009090737],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9998447,0.000024609873,0.000009845643,0.00005902369,0.00003359571,0.000028125467],"domain_scores_gemma":[0.99981207,0.00005510691,0.000069834336,0.000015494421,0.000014865398,0.00003264783],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00015604765,0.00016175944,0.00018978833,0.0005444753,0.00014557828,0.00018741372,0.00013695915,0.00022295503,0.0008697316],"category_scores_gemma":[0.00017546595,0.00019942733,0.00015116773,0.00016499558,0.00031291638,0.00011057617,0.00018732762,0.00019649604,0.0001719989],"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":[0.00026676265,0.0000075641983,0.01592079,0.000019301495,0.000015068649,0.0004622846,0.00009426901,0.000026843332,0.980628,0.00006554961,0.0000123093505,0.0024812866],"study_design_scores_gemma":[0.000031230364,0.00046926015,0.85967237,0.000013743228,0.000085545544,0.0060783066,0.0002516919,0.00036636658,0.13134754,0.00018171078,0.0014795761,0.000022640868],"about_ca_topic_score_codex":0.00055066514,"about_ca_topic_score_gemma":0.0011315531,"teacher_disagreement_score":0.0008697316,"about_ca_system_score_codex":0.00010583379,"about_ca_system_score_gemma":0.00008734078,"threshold_uncertainty_score":0.0029094815},"labels":[],"label_agreement":null},{"id":"W1984678352","doi":"10.1016/j.placenta.2006.01.015","title":"Epigenetics and Imprinting of the Trophoblast – A Workshop Report","year":2006,"lang":"en","type":"article","venue":"Placenta","topic":"Genetic Syndromes and Imprinting","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":"Mount Sinai Hospital","funders":"Biotechnology and Biological Sciences Research Council","keywords":"Genomic imprinting; Imprinting (psychology); Epigenetics; Trophoblast; Placenta; Biology; Genetics; Gene; DNA methylation; Bioinformatics; Gene expression; Pregnancy; Fetus","score_opus":0.005609102866246421,"score_gpt":0.2138508686830016,"score_spread":0.2082417658167552,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1984678352","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":[0.07198303,0.7227632,0.023181481,0.06771834,0.069290906,0.00039589664,0.0010988008,0.00027917093,0.043289166],"genre_scores_gemma":[0.28941798,0.47245362,0.012708799,0.013144243,0.082544014,0.0005420745,0.0020196985,0.00022344927,0.12694605],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.99930227,0.00016550731,0.000045741257,0.00016187235,0.00015211591,0.00017243173],"domain_scores_gemma":[0.9992805,0.00014916123,0.0000396579,0.000033329503,0.00015342323,0.00034388498],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.002956559,0.0013006119,0.0005375043,0.0010528404,0.00084369804,0.002559036,0.0015302306,0.0032065073,0.0038595118],"category_scores_gemma":[0.00093464553,0.00036844824,0.00069841766,0.00065485074,0.0010557601,0.0019125356,0.0036497756,0.0028857547,0.0015548998],"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":[0.0028382207,0.0009075276,0.003642285,0.004006298,0.00037975187,0.011478154,0.0040009525,0.0029009806,0.13491847,0.030906156,0.39394104,0.41008008],"study_design_scores_gemma":[0.00011886229,0.0006449972,0.0030440574,0.00061008777,0.00014329274,0.004141065,0.0015374606,0.0006206469,0.043792434,0.006934043,0.9383309,0.00008207088],"about_ca_topic_score_codex":0.0010381398,"about_ca_topic_score_gemma":0.0014976913,"teacher_disagreement_score":0.0038595118,"about_ca_system_score_codex":0.000931312,"about_ca_system_score_gemma":0.0014356184,"threshold_uncertainty_score":0.015635967},"labels":[],"label_agreement":null},{"id":"W1985679507","doi":"10.1007/s10735-011-9367-x","title":"Spatiotemporal expression pattern of Mirg, an imprinted non-coding gene, during mouse embryogenesis","year":2011,"lang":"en","type":"article","venue":"Journal of Molecular Histology","topic":"Genetic Syndromes and Imprinting","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":"Princess Margaret Cancer Centre","funders":"","keywords":"Biology; Embryogenesis; MEG3; Gene silencing; Gene expression; Gene; In situ hybridization; Embryonic stem cell; Genomic imprinting; Embryo; Cell biology; Developmental biology; RNA; Molecular biology; Genetics; Long non-coding RNA","score_opus":0.013257861066157513,"score_gpt":0.22818592376859867,"score_spread":0.21492806270244116,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1985679507","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.98471606,0.0048562204,0.0046285205,0.00011325949,0.000025251324,0.000014789646,0.0008434875,0.00014789667,0.004654557],"genre_scores_gemma":[0.9893811,0.0011601066,0.002557072,0.000076072036,0.000012903706,0.000029434887,0.00062382064,0.000057143687,0.006102388],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.99984705,0.000017186565,0.0000120258555,0.000050334897,0.000034413195,0.000038895945],"domain_scores_gemma":[0.99974734,0.000047270038,0.00008229407,0.000020901867,0.00003752364,0.000064584],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00017902147,0.00017182973,0.00025029652,0.00085418724,0.00021172765,0.00050223665,0.00019191288,0.0003197747,0.0006465285],"category_scores_gemma":[0.00020060247,0.00033630405,0.00017396711,0.0003302308,0.0003435218,0.00034746918,0.00026500382,0.0004973507,0.00043125686],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00036500068,0.000009962854,0.0022971663,0.00002988918,0.000007890337,0.00017623344,0.000094377836,0.000100424455,0.9938834,0.0006351114,0.00008565463,0.0023148365],"study_design_scores_gemma":[0.000036522368,0.00021870062,0.10184022,0.00003440386,0.000066064,0.0010657433,0.00022364258,0.0014442474,0.88889444,0.0004884412,0.005662752,0.000024802986],"about_ca_topic_score_codex":0.0010640561,"about_ca_topic_score_gemma":0.0013955049,"teacher_disagreement_score":0.0010640561,"about_ca_system_score_codex":0.000405889,"about_ca_system_score_gemma":0.00018571915,"threshold_uncertainty_score":0.0029449463},"labels":[],"label_agreement":null},{"id":"W1985876152","doi":"10.1017/s0140525x01273968","title":"Genomic imprinting and culture in mammals","year":2001,"lang":"en","type":"article","venue":"Behavioral and Brain Sciences","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","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":"Dalhousie University","funders":"","keywords":"Imprinting (psychology); Receptivity; Genomic imprinting; Biology; Genomic information; Evolutionary biology; Gene; Psychology; Genetics; Genome; Gene expression","score_opus":0.02694687285279374,"score_gpt":0.3011778499987616,"score_spread":0.2742309771459679,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1985876152","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.8870252,0.058725987,0.0143374875,0.0013102037,0.000084977706,0.000018004668,0.00027595682,0.00020213822,0.038019974],"genre_scores_gemma":[0.9856543,0.0090316525,0.0022055372,0.00020804045,0.00007316772,0.000009118092,0.00011782635,0.000013776393,0.0026866214],"study_design_codex":"design_other","study_design_gemma":"theoretical_or_conceptual","domain_scores_codex":[0.99988747,0.000025625408,0.000007996599,0.000037002887,0.000023255157,0.000018638597],"domain_scores_gemma":[0.9997819,0.00007149923,0.00007339134,0.000022366556,0.000013419953,0.000037401354],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00017782244,0.00012390476,0.0002200891,0.00042099538,0.00029480754,0.00052296603,0.00032394228,0.00032779487,0.0008463383],"category_scores_gemma":[0.00048822624,0.000117942596,0.00009164785,0.0004426466,0.0014792939,0.00046769326,0.0005775294,0.0003236203,0.00020100379],"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":[0.00044913898,0.00007241205,0.065702714,0.000695392,0.00020331115,0.0051251114,0.0035197446,0.008830223,0.32406583,0.15348521,0.0022398687,0.43561104],"study_design_scores_gemma":[0.000058932954,0.0005472191,0.6424258,0.0002346064,0.00017274887,0.009638908,0.0012861617,0.0044302414,0.04003574,0.19795015,0.10306978,0.00014980568],"about_ca_topic_score_codex":0.0011673867,"about_ca_topic_score_gemma":0.001301064,"teacher_disagreement_score":0.0011673867,"about_ca_system_score_codex":0.0003056664,"about_ca_system_score_gemma":0.00017030786,"threshold_uncertainty_score":0.0028312206},"labels":[],"label_agreement":null},{"id":"W1986515247","doi":"10.1016/j.jpeds.2008.12.033","title":"Body mass index in children with Prader-Willi Syndrome during human growth hormone therapy: A real world situation","year":2009,"lang":"en","type":"letter","venue":"The Journal of Pediatrics","topic":"Genetic Syndromes and Imprinting","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":"BC Children's Hospital","funders":"","keywords":"Medicine; Body mass index; Human growth hormone; Growth hormone; Index (typography); Pediatrics; Endocrinology; Hormone","score_opus":0.007093148032011679,"score_gpt":0.21984410935736265,"score_spread":0.21275096132535096,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1986515247","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.84557396,0.0031367466,0.00062746415,0.13654947,0.0025397532,0.000038393828,0.0004639643,0.00007911368,0.010991026],"genre_scores_gemma":[0.98085725,0.0015565986,0.00051048346,0.012344555,0.0034902983,0.000016381266,0.00015667714,0.00002705186,0.0010406942],"study_design_codex":"case_report","study_design_gemma":"observational","domain_scores_codex":[0.9993655,0.00016701015,0.00009320529,0.000112095164,0.00013781183,0.0001243894],"domain_scores_gemma":[0.9964066,0.0017043619,0.0006440904,0.00010536541,0.00023317958,0.0009063446],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00052490947,0.0005798695,0.00088789675,0.001012616,0.001355541,0.0010549542,0.00083167566,0.006083173,0.0011954415],"category_scores_gemma":[0.00565412,0.00038532124,0.0005314742,0.001384999,0.0011881618,0.0009855805,0.00052666076,0.0044609793,0.00023144642],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00039511095,0.00009118944,0.2955901,0.000051193194,0.000052728454,0.6851558,0.0008292254,0.00023287261,0.0011327614,0.00093081244,0.00967506,0.0058631166],"study_design_scores_gemma":[0.00010827206,0.0004541241,0.27357277,0.00011791879,0.000108214444,0.71213603,0.0026534728,0.0014307956,0.00048153393,0.0013691316,0.007499465,0.00006821974],"about_ca_topic_score_codex":0.0048203752,"about_ca_topic_score_gemma":0.006399939,"teacher_disagreement_score":0.006083173,"about_ca_system_score_codex":0.0014953399,"about_ca_system_score_gemma":0.0007419618,"threshold_uncertainty_score":0.010849535},"labels":[],"label_agreement":null},{"id":"W1987171500","doi":"10.1002/ajmg.a.35377","title":"Beckwith–Wiedemann syndrome in sibs discordant for IC2 methylation","year":2012,"lang":"en","type":"article","venue":"American Journal of Medical Genetics Part A","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":9,"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; University of Toronto; University of British Columbia; Hospital for Sick Children; Rare Disease Foundation; Child and Family Research Institute","funders":"Division of Materials Research; Canadian Institutes of Health Research","keywords":"DNA methylation; Genomic imprinting; Epigenetics; Biology; Beckwith–Wiedemann syndrome; Methylation; Genetics; Methylated DNA immunoprecipitation; CpG site; Differentially methylated regions; Imprinting (psychology); Molecular biology; Gene; Gene expression","score_opus":0.016458215481712245,"score_gpt":0.3035539655127694,"score_spread":0.2870957500310572,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1987171500","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99848336,0.00012313781,0.00033082266,0.000054632692,0.000013508025,0.00000876451,0.00006760458,0.000018636754,0.00089964585],"genre_scores_gemma":[0.99945956,0.000062656385,0.00024599518,0.00002517674,0.0000082662145,0.0000037131445,0.000054623244,0.0000037971845,0.00013626313],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99972206,0.000053291147,0.000034955854,0.00007090726,0.00006519587,0.000053667743],"domain_scores_gemma":[0.99969995,0.000096449665,0.000079605095,0.000022188056,0.000016274422,0.000085509506],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00023081747,0.000670103,0.0003851402,0.0014201237,0.00077694794,0.00038758677,0.0002807715,0.0006149532,0.0021375308],"category_scores_gemma":[0.001280529,0.00036681833,0.0003166563,0.0006305637,0.00057271007,0.00017203564,0.0005816458,0.00041286956,0.00034211125],"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":[0.00061171706,0.00015361817,0.58392256,0.00007396086,0.00013241351,0.31379783,0.0024439483,0.00042907827,0.08316031,0.0007998918,0.00066698436,0.013807598],"study_design_scores_gemma":[0.00005735093,0.00039340337,0.40890086,0.00004289127,0.00016821145,0.5666879,0.00089583156,0.0011303094,0.019053152,0.0007048378,0.0019238943,0.00004142846],"about_ca_topic_score_codex":0.0021055108,"about_ca_topic_score_gemma":0.0029900442,"teacher_disagreement_score":0.0021375308,"about_ca_system_score_codex":0.00024095671,"about_ca_system_score_gemma":0.00025875456,"threshold_uncertainty_score":0.0071507692},"labels":[],"label_agreement":null},{"id":"W1987244404","doi":"10.1007/s10508-011-9805-6","title":"New MRI Studies Support the Blanchard Typology of Male-to-Female Transsexualism","year":2011,"lang":"en","type":"letter","venue":"Archives of Sexual Behavior","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":14,"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","funders":"","keywords":"Typology; Sexual behavior; Psychology; Public health; Adult male; Clinical psychology; Developmental psychology; Medicine; Internal medicine; Pathology; Sociology","score_opus":0.04285654855545794,"score_gpt":0.2998062101823736,"score_spread":0.2569496616269156,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1987244404","genre_codex":"empirical","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":[0.5428973,0.09335015,0.039942447,0.025678907,0.003166113,0.0003089473,0.0014759045,0.000352861,0.29282746],"genre_scores_gemma":[0.92203003,0.04094856,0.011894813,0.004820777,0.0010182292,0.00010525795,0.00049103575,0.0001087699,0.018582433],"study_design_codex":"design_other","study_design_gemma":"observational","domain_scores_codex":[0.9995005,0.000070250695,0.000038397702,0.00016182281,0.0001764816,0.000052584644],"domain_scores_gemma":[0.99781287,0.0007559529,0.0006891315,0.00035035756,0.000248996,0.00014262887],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0014281704,0.00073557073,0.00046406104,0.0022449263,0.00096311094,0.001379182,0.0009121682,0.0011988848,0.014734221],"category_scores_gemma":[0.0029505629,0.0002915062,0.00036041925,0.001424039,0.003556936,0.0024585498,0.0012352802,0.0017906484,0.0019583092],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0011986766,0.00067654025,0.272583,0.0023828498,0.0004997519,0.015576025,0.018023964,0.0004917314,0.022676222,0.15424968,0.032581694,0.47905985],"study_design_scores_gemma":[0.000121175544,0.0006963366,0.39144745,0.0016091879,0.00027838277,0.10679644,0.013802182,0.00094533985,0.011359863,0.12445664,0.3482416,0.0002454485],"about_ca_topic_score_codex":0.0023849448,"about_ca_topic_score_gemma":0.0053869127,"teacher_disagreement_score":0.014734221,"about_ca_system_score_codex":0.0006506612,"about_ca_system_score_gemma":0.0004415643,"threshold_uncertainty_score":0.049290836},"labels":[],"label_agreement":null},{"id":"W1987825638","doi":"10.2337/db11-1314","title":"Transgenerational Glucose Intolerance With <i>Igf2</i>/<i>H19</i> Epigenetic Alterations in Mouse Islet Induced by Intrauterine Hyperglycemia","year":2012,"lang":"en","type":"article","venue":"Diabetes","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":310,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Child and Family Research Institute; University of British Columbia","funders":"","keywords":"Offspring; Impaired glucose tolerance; Gestational diabetes; Genomic imprinting; Endocrinology; Epigenetics; Internal medicine; Biology; Islet; Diabetes mellitus; DNA methylation; Pregnancy; Gestation; Type 2 diabetes; Gene; Medicine; Gene expression; Genetics","score_opus":0.007940225014701258,"score_gpt":0.2156889418735279,"score_spread":0.20774871685882665,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1987825638","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9942456,0.00058659085,0.0033555944,0.0000729683,0.000050342867,0.000030771393,0.0006219453,0.00012093026,0.00091519003],"genre_scores_gemma":[0.98902065,0.0008354404,0.0035760764,0.00013882651,0.000022064074,0.000120711564,0.0011658149,0.00009718021,0.0050232136],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9997565,0.000021928707,0.000028583572,0.00008816107,0.000047931517,0.00005689664],"domain_scores_gemma":[0.9997975,0.000017372846,0.00007467284,0.000031632644,0.0000114518,0.00006734],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00017933139,0.00041559656,0.00023871052,0.0005196252,0.00018101947,0.00022772673,0.00029772334,0.00030860305,0.0016016763],"category_scores_gemma":[0.000095986834,0.00024071561,0.00045972815,0.00023663547,0.00031661344,0.00017172916,0.00031082617,0.00086772465,0.00024420905],"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":[0.00014320848,0.00003394309,0.00084338605,0.000017576962,0.000008092973,0.00009259321,0.000028024037,0.000024542527,0.99776304,0.00010460434,0.000026365995,0.00091463607],"study_design_scores_gemma":[0.000048039543,0.00071103894,0.033655047,0.000014644137,0.000059792168,0.0007139332,0.00008720417,0.0005968874,0.96092904,0.00010043181,0.0030698036,0.000014102376],"about_ca_topic_score_codex":0.00068694184,"about_ca_topic_score_gemma":0.0013144999,"teacher_disagreement_score":0.0016016763,"about_ca_system_score_codex":0.0002337143,"about_ca_system_score_gemma":0.00016926156,"threshold_uncertainty_score":0.0053581},"labels":[],"label_agreement":null},{"id":"W1988289925","doi":"10.1097/01.mop.0000187191.74295.97","title":"Advances in overgrowth syndromes: clinical classification to molecular delineation in Sotos syndrome and Beckwith-Wiedemann syndrome","year":2005,"lang":"en","type":"review","venue":"Current Opinion in Pediatrics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":23,"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; SickKids Foundation; University of Toronto; Hospital for Sick Children","funders":"","keywords":"Sotos syndrome; Medicine; Bioinformatics; Pediatrics; Biology","score_opus":0.08456372896538565,"score_gpt":0.42098775594155646,"score_spread":0.3364240269761708,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1988289925","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":[0.00039360824,0.9970573,0.00044117236,0.0006274218,0.0005530454,0.000008577264,0.000012479062,0.000013841177,0.00089262164],"genre_scores_gemma":[0.0023547958,0.99443024,0.0014507899,0.00048024274,0.00061931775,0.000014393006,0.00004738506,0.0000037127909,0.00059923896],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.99958867,0.000103891296,0.00008359787,0.000060226554,0.00013366126,0.000029818486],"domain_scores_gemma":[0.99951494,0.00016801334,0.000109229055,0.000018072613,0.0001384433,0.000051219187],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00076951255,0.0010943578,0.001750901,0.0020578054,0.00023334444,0.000823536,0.00097293453,0.0011159207,0.0016402487],"category_scores_gemma":[0.001406187,0.00020644708,0.00040434249,0.0022591238,0.0006568513,0.0012130926,0.0006058412,0.0013709592,0.0015883597],"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":[0.000111986104,0.000048311875,0.0014181334,0.010206783,0.00010271925,0.0025163158,0.0001392049,0.00042939957,0.003353632,0.0049053594,0.0322879,0.94448024],"study_design_scores_gemma":[0.00005482635,0.00014479658,0.0058991653,0.004921211,0.00021028957,0.03657258,0.000302588,0.0002583608,0.0011391045,0.0036704629,0.94677806,0.000048451497],"about_ca_topic_score_codex":0.0011025324,"about_ca_topic_score_gemma":0.0014188247,"teacher_disagreement_score":0.0020578054,"about_ca_system_score_codex":0.00072353176,"about_ca_system_score_gemma":0.0011352759,"threshold_uncertainty_score":0.0054872036},"labels":[],"label_agreement":null},{"id":"W1989369027","doi":"10.1093/hmg/ddi059","title":"Essential role for the Prader–Willi syndrome protein necdin in axonal outgrowth","year":2005,"lang":"en","type":"article","venue":"Human Molecular Genetics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":133,"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":"","keywords":"Biology; Cell biology; Genetics; Neuroscience","score_opus":0.009450473847293918,"score_gpt":0.25020741792656936,"score_spread":0.24075694407927545,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1989369027","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9954963,0.0011356054,0.0017477659,0.00009315041,0.0000103966095,0.0000039543133,0.000085835294,0.000041647963,0.0013853445],"genre_scores_gemma":[0.99699914,0.00042826997,0.0013793032,0.000017021623,0.000003458855,0.0000080040045,0.00013606763,0.000007655196,0.0010211887],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99990463,0.00002282782,0.000010542392,0.00001854406,0.000027312466,0.000016167724],"domain_scores_gemma":[0.99989426,0.00002478563,0.000029079156,0.000016249822,0.000008369551,0.000027246155],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0000847555,0.00029597688,0.00013847456,0.00017350576,0.00015502656,0.00021036352,0.0001894627,0.00026994973,0.0011792437],"category_scores_gemma":[0.00019238648,0.00014952983,0.00010623783,0.00006534377,0.00029916392,0.00021158859,0.00043210658,0.0002751054,0.0005761511],"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":[0.000070353984,0.000007091656,0.00070396735,0.000026559483,0.0000050636563,0.00082337845,0.000011214911,0.00013919518,0.9964592,0.00035050412,0.000034335106,0.0013690914],"study_design_scores_gemma":[0.000057862544,0.000224657,0.045278717,0.000018616362,0.000029978442,0.011957273,0.000059669583,0.0037952578,0.93231267,0.00050848076,0.00574589,0.000010870443],"about_ca_topic_score_codex":0.00037917844,"about_ca_topic_score_gemma":0.00071631843,"teacher_disagreement_score":0.0011792437,"about_ca_system_score_codex":0.00026641056,"about_ca_system_score_gemma":0.00020249035,"threshold_uncertainty_score":0.003944993},"labels":[],"label_agreement":null},{"id":"W1990582768","doi":"10.1016/j.jpeds.2010.01.018","title":"Non-Immune Goiter and Hypothyroidism in a 19-Week Fetus: A Plea for Conservative Treatment","year":2010,"lang":"en","type":"article","venue":"The Journal of Pediatrics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","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":"Centre Hospitalier Universitaire Sainte-Justine; Université de Montréal","funders":"Canadian Child Health Clinician Scientist Program","keywords":"Medicine; Polyhydramnios; Amniotic fluid; Fetus; Goiter; Psychomotor learning; Obstetrics; Pregnancy; Internal medicine; Endocrinology; Thyroid","score_opus":0.012848678023731453,"score_gpt":0.24863960195418663,"score_spread":0.23579092393045517,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1990582768","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.80923384,0.01381822,0.0059053143,0.12094464,0.0034626194,0.0005488125,0.0006122303,0.00047199888,0.04500217],"genre_scores_gemma":[0.9676695,0.0056165187,0.004459143,0.008404522,0.0070099775,0.0000881241,0.00020875878,0.00012792423,0.0064154337],"study_design_codex":"case_report","study_design_gemma":"case_report","domain_scores_codex":[0.9996019,0.00003835146,0.000055183984,0.00007764945,0.00007084655,0.00015606955],"domain_scores_gemma":[0.998574,0.00054388115,0.00016907879,0.00008250267,0.00006588435,0.0005647204],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00034208925,0.0015342137,0.0011762786,0.0020838461,0.0031910948,0.0010292493,0.0016784526,0.009905511,0.0037979216],"category_scores_gemma":[0.004174409,0.0007778036,0.0012258564,0.0005420553,0.0020370288,0.0012938343,0.0011306744,0.0060073077,0.000748775],"study_design_candidate":"case_report","study_design_consensus":"case_report","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.000020561898,0.000017389753,0.000978322,0.000007960911,0.000001654572,0.99779344,0.000018691351,0.000029328268,0.00031560162,0.00013368794,0.0001755581,0.00050783146],"study_design_scores_gemma":[0.000014030586,0.00008283192,0.0024563381,0.000027073202,0.000009554752,0.99555796,0.00013926745,0.00016563862,0.00047000233,0.000376258,0.00069216645,0.000008966448],"about_ca_topic_score_codex":0.0027134793,"about_ca_topic_score_gemma":0.004053081,"teacher_disagreement_score":0.009905511,"about_ca_system_score_codex":0.0018483988,"about_ca_system_score_gemma":0.0014829166,"threshold_uncertainty_score":0.013411164},"labels":[],"label_agreement":null},{"id":"W1990626904","doi":"10.1371/journal.pgen.1002600","title":"Critical Evaluation of Imprinted Gene Expression by RNA–Seq: A New Perspective","year":2012,"lang":"en","type":"article","venue":"PLoS Genetics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":230,"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","funders":"Canadian Institutes of Health Research","keywords":"Biology; Genomic imprinting; Genetics; Allele; Gene; Computational biology; False positive paradox; Concordance; RNA-Seq; Transcriptome; Pyrosequencing; Gene expression; DNA methylation; Statistics","score_opus":0.03333032953320142,"score_gpt":0.3172731554300056,"score_spread":0.2839428258968042,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1990626904","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":[0.096394785,0.007867303,0.88902193,0.0025475177,0.00073432975,0.0001870332,0.00082959206,0.0006555664,0.0017620561],"genre_scores_gemma":[0.49689117,0.007486414,0.48848492,0.0026074776,0.0008632623,0.0004677126,0.0008552889,0.00068784977,0.0016558606],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9950563,0.0020643345,0.0003052195,0.00083260774,0.0016168499,0.00012469497],"domain_scores_gemma":[0.9827786,0.011081603,0.0007912764,0.0027705436,0.0022603017,0.00031771554],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.016930746,0.001045759,0.0017011152,0.00093291857,0.0004937897,0.002460947,0.0013567145,0.00079837,0.00085636444],"category_scores_gemma":[0.017534774,0.0005209007,0.0006720223,0.00075652107,0.002221528,0.0022684215,0.0011450289,0.002553922,0.00025585198],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00043278636,0.00017374115,0.013062277,0.0011330654,0.00048164366,0.00035196127,0.00094774674,0.014222453,0.8359687,0.019373905,0.0016404082,0.112211294],"study_design_scores_gemma":[0.000055771445,0.0010702462,0.05247729,0.00043752827,0.00043759544,0.0011710483,0.0010321533,0.22535878,0.59854645,0.08618715,0.032813646,0.0004123979],"about_ca_topic_score_codex":0.00077630114,"about_ca_topic_score_gemma":0.0018021171,"teacher_disagreement_score":0.016930746,"about_ca_system_score_codex":0.0008242897,"about_ca_system_score_gemma":0.00088267616,"threshold_uncertainty_score":0.08953941},"labels":[],"label_agreement":null},{"id":"W1991089031","doi":"10.1002/ajmg.a.32283","title":"Sotos syndrome: Antenatal presentation","year":2008,"lang":"en","type":"article","venue":"American Journal of Medical Genetics Part A","topic":"Genetic Syndromes and Imprinting","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 Saskatchewan; Izaak Walton Killam Health Centre","funders":"","keywords":"Sotos syndrome; Macrocephaly; Presentation (obstetrics); Medicine; Pregnancy; Polyhydramnios; Pediatrics; Differential diagnosis; Obstetrics; Fetus; Pathology; Biology; Genetics","score_opus":0.013302933233658495,"score_gpt":0.27514576478104585,"score_spread":0.26184283154738736,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1991089031","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.96921754,0.006773314,0.0025848346,0.0025424657,0.00040095663,0.000088356115,0.0004249373,0.00028083078,0.017686667],"genre_scores_gemma":[0.9945155,0.0030230868,0.0006940615,0.00031918165,0.0003339,0.000016591353,0.00010350577,0.000016497099,0.0009777559],"study_design_codex":"case_report","study_design_gemma":"case_report","domain_scores_codex":[0.9997646,0.00003545289,0.000023090963,0.00004749426,0.00007003798,0.00005923803],"domain_scores_gemma":[0.9991049,0.00027405444,0.00029814587,0.000040482442,0.00004882714,0.00023351646],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0001273884,0.0006263798,0.0005443152,0.0010939263,0.00033354165,0.00050895684,0.00038907293,0.0012979042,0.002184096],"category_scores_gemma":[0.002409825,0.00020723832,0.00021887326,0.000573313,0.00049095636,0.0003795222,0.00053677656,0.00060943735,0.00035135922],"study_design_candidate":"case_report","study_design_consensus":"case_report","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00015563623,0.000043237003,0.049903862,0.00013800629,0.000020804024,0.9176525,0.0005321017,0.000204562,0.01441503,0.0013638461,0.0016612782,0.0139091285],"study_design_scores_gemma":[0.000012058004,0.0000900366,0.018338028,0.000054203432,0.00001805304,0.97730756,0.00013850826,0.00018861264,0.0011127238,0.0006406341,0.0020831556,0.000016351692],"about_ca_topic_score_codex":0.000803606,"about_ca_topic_score_gemma":0.00055161153,"teacher_disagreement_score":0.002184096,"about_ca_system_score_codex":0.0002255335,"about_ca_system_score_gemma":0.0002611953,"threshold_uncertainty_score":0.007306516},"labels":[],"label_agreement":null},{"id":"W1992543365","doi":"10.1002/ajmg.1587","title":"Linkage study in families with posterior helical ear pits and Wiedemann-Beckwith Syndrome","year":2001,"lang":"en","type":"article","venue":"American Journal of Medical Genetics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":11,"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; University of Toronto; Toronto Western Hospital; Hospital for Sick Children","funders":"","keywords":"Pedigree chart; Genetics; Beckwith–Wiedemann syndrome; Genetic linkage; Biology; Penetrance; Haplotype; Phenotype; Linkage (software); Gene; Allele","score_opus":0.007550696874891125,"score_gpt":0.26074247557279473,"score_spread":0.2531917786979036,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1992543365","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99857366,0.0002758633,0.00039353318,0.000040377196,0.0000088805855,0.000014035236,0.000104095576,0.000009248316,0.00058036874],"genre_scores_gemma":[0.99857163,0.00029179957,0.00052702957,0.00004534156,0.000012085359,0.000018614139,0.00023865986,0.0000047238022,0.00029010064],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99924123,0.00024787037,0.00006232355,0.0002075123,0.0001309404,0.00011021609],"domain_scores_gemma":[0.99952865,0.00015351095,0.000104128674,0.000039113325,0.000046600275,0.000127963],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0006196653,0.0007287154,0.00047974839,0.0014937274,0.0012009346,0.00039176588,0.00027060916,0.0005049603,0.0023920496],"category_scores_gemma":[0.0019286841,0.00037370546,0.0004553415,0.0010688493,0.00038866053,0.00021845545,0.0006900944,0.00031149364,0.0002514566],"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":[0.0013236713,0.0005073006,0.88007814,0.00009853041,0.00050771324,0.05858892,0.0044883206,0.0005425753,0.03040884,0.0012960135,0.0013297141,0.020830352],"study_design_scores_gemma":[0.00021471143,0.0013104253,0.8998984,0.000119690594,0.0004916123,0.08588558,0.0014363138,0.0012672284,0.0034156367,0.0006367201,0.0052689337,0.000054702483],"about_ca_topic_score_codex":0.0063228495,"about_ca_topic_score_gemma":0.0037876104,"teacher_disagreement_score":0.0063228495,"about_ca_system_score_codex":0.00038864271,"about_ca_system_score_gemma":0.00037491997,"threshold_uncertainty_score":0.01257211},"labels":[],"label_agreement":null},{"id":"W1993696633","doi":"10.1159/000133352","title":"Localization of mouse parathyroid hormone-like peptide gene (Pthlh) to distal chromosome 6 using interspecific backcross mice and in situ hybridization","year":2008,"lang":"en","type":"article","venue":"Cytogenetics and Cell Genetics","topic":"Genetic Syndromes and Imprinting","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":"McGill University; Royal Victoria Hospital; Royal Victoria Regional Health Centre","funders":"National Human Genome Research Institute; Kementerian Pendidikan Nasional","keywords":"Biology; Molecular biology; Locus (genetics); Chromosome 17 (human); Genetics; Gene; Chromosome","score_opus":0.015799603880987338,"score_gpt":0.23001029173731763,"score_spread":0.2142106878563303,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1993696633","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.94857323,0.0020971373,0.040265694,0.0002029972,0.0000920013,0.00014061366,0.001027255,0.00037800297,0.007222998],"genre_scores_gemma":[0.94861144,0.00428488,0.026888536,0.000116744835,0.000049800725,0.00016131344,0.0027367568,0.00016027346,0.016990181],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9996412,0.000039691175,0.000027545551,0.000131896,0.00010424861,0.000055446228],"domain_scores_gemma":[0.9997569,0.000054491706,0.00007873416,0.00004206506,0.000017470527,0.000050317158],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00026670154,0.0005356391,0.00026537018,0.0012806639,0.0003770706,0.0003824596,0.0005197689,0.00038900672,0.0036886695],"category_scores_gemma":[0.00019966495,0.00039109009,0.00033230506,0.00039423179,0.0004115563,0.00019268644,0.00056848215,0.00083159714,0.00091557845],"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":[0.000033668726,0.000011075482,0.00015380062,0.000016611544,0.0000047261974,0.000077871635,0.000014550993,0.000036005124,0.99863005,0.00012505917,0.000015569767,0.00088102766],"study_design_scores_gemma":[0.0000237376,0.00018603247,0.007308249,0.000015193224,0.00004996473,0.0015788317,0.00003970655,0.00043001614,0.9851039,0.00012488484,0.005130874,0.0000086810705],"about_ca_topic_score_codex":0.0006908285,"about_ca_topic_score_gemma":0.0014812449,"teacher_disagreement_score":0.0036886695,"about_ca_system_score_codex":0.00025205957,"about_ca_system_score_gemma":0.0001524966,"threshold_uncertainty_score":0.01233983},"labels":[],"label_agreement":null},{"id":"W1993901957","doi":"10.1111/j.1365-2052.2008.01838.x","title":"<i>TCOF1 T</i>/<i>Ser</i> variant and brachycephaly in dogs","year":2009,"lang":"he","type":"article","venue":"Animal Genetics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":9,"is_retracted":false,"has_abstract":true,"route_ca_aff":false,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":true,"ca_institutions":"","funders":"National Key Research and Development Program of China","keywords":"Biology; Genetics; Polymorphism (computer science); Genotype; Gene","score_opus":0.008933073643971957,"score_gpt":0.2400342641506596,"score_spread":0.23110119050668765,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1993901957","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9985051,0.00021918089,0.00010331368,0.00008051365,0.000010922036,0.000002654399,0.00034535144,0.0000053524436,0.0007276696],"genre_scores_gemma":[0.99891543,0.00016490041,0.00008831292,0.000021067453,0.000019115023,0.0000022674305,0.00028923404,0.0000043062873,0.00049530336],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9998907,0.000019558194,0.0000123035725,0.000034754048,0.000022796175,0.000019948171],"domain_scores_gemma":[0.9997558,0.00007458936,0.00010498263,0.00001147128,0.000015745405,0.000037394137],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00015890328,0.00024338528,0.0001806131,0.0011610239,0.00025100174,0.00017996518,0.00019035052,0.00036939254,0.00513878],"category_scores_gemma":[0.00058362575,0.00013027086,0.00018111683,0.00090457726,0.00038125922,0.00011688178,0.00013529624,0.00020709354,0.00029747252],"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":[0.0062287473,0.00016329912,0.8565028,0.000115954885,0.00024148756,0.038373034,0.0008882608,0.0006540754,0.07435079,0.0010542183,0.0038769855,0.01755031],"study_design_scores_gemma":[0.000053206728,0.00028052056,0.96074283,0.000032645752,0.00009399551,0.033211213,0.00033178434,0.00046606763,0.0024656306,0.00025069533,0.0020571195,0.000014229729],"about_ca_topic_score_codex":0.005332898,"about_ca_topic_score_gemma":0.0031447038,"teacher_disagreement_score":0.005332898,"about_ca_system_score_codex":0.00015339644,"about_ca_system_score_gemma":0.00010172825,"threshold_uncertainty_score":0.017190933},"labels":[],"label_agreement":null},{"id":"W1994577070","doi":"10.1006/bbrc.1999.1982","title":"Methylation Patterns of Human Parathyroid Hormone (PTH)/PTH-Related Peptide Receptor Gene Promoters Are Established Several Weeks Prior to Onset of Their Function","year":2000,"lang":"en","type":"article","venue":"Biochemical and Biophysical Research Communications","topic":"Genetic Syndromes and Imprinting","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":"Montreal Children's Hospital; Jewish General Hospital; Royal Victoria Hospital; McGill University","funders":"","keywords":"Methylation; Promoter; CpG site; Parathyroid hormone; DNA methylation; Endocrinology; Biology; Internal medicine; Receptor; Kidney; Demethylation; Parathyroid hormone receptor; Gene; Gene expression; Hormone receptor; Genetics; Medicine; Calcium; Cancer","score_opus":0.03458819274314194,"score_gpt":0.31331456998512397,"score_spread":0.278726377241982,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1994577070","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9905275,0.001541863,0.004000341,0.0001066966,0.000029414157,0.000019717303,0.0009302002,0.00009864623,0.0027455867],"genre_scores_gemma":[0.9937429,0.0003546458,0.00094079477,0.000044543358,0.0000137192665,0.000026303274,0.00071658625,0.0000307121,0.004129793],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.99986386,0.000017675728,0.0000074881077,0.000045686375,0.000027749116,0.000037504185],"domain_scores_gemma":[0.9996942,0.000105260966,0.00006416495,0.000030499123,0.000044186054,0.00006174462],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00015786994,0.0001481026,0.00023849693,0.0004567737,0.00016366683,0.00034487442,0.00021886721,0.00020820425,0.0024189062],"category_scores_gemma":[0.00054752076,0.0003502534,0.00020489824,0.0001525833,0.00025959176,0.00022714598,0.00024978514,0.00051685993,0.000741626],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0004188721,0.000013760829,0.003566773,0.00001565742,0.000009803668,0.00006980992,0.00010179073,0.000040751343,0.992644,0.00019767492,0.000056320692,0.002864809],"study_design_scores_gemma":[0.00003677902,0.00033093165,0.35850433,0.000016677186,0.000047028032,0.0009366463,0.00025958853,0.000829825,0.6348292,0.0004609374,0.003724796,0.000023323408],"about_ca_topic_score_codex":0.002366072,"about_ca_topic_score_gemma":0.0040105465,"teacher_disagreement_score":0.0024189062,"about_ca_system_score_codex":0.00027716657,"about_ca_system_score_gemma":0.00016680604,"threshold_uncertainty_score":0.008092046},"labels":[],"label_agreement":null},{"id":"W1996207676","doi":"10.1139/g06-042","title":"Loss of genomic imprinting in<i>Drosophila</i>clones","year":2006,"lang":"en","type":"article","venue":"Genome","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":4,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":true,"route_about_ca":false,"ca_institutions":"Dalhousie University","funders":"","keywords":"Biology; Genomic imprinting; Imprinting (psychology); Genetics; Evolutionary biology; Gene; DNA methylation; Gene expression","score_opus":0.006412581397798147,"score_gpt":0.21114850784494216,"score_spread":0.204735926447144,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1996207676","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9636808,0.0017369782,0.018214826,0.00039676588,0.00011777707,0.00019398775,0.0029921783,0.00026077955,0.012406015],"genre_scores_gemma":[0.95356005,0.001484174,0.016647143,0.000300173,0.00002327045,0.00014712258,0.0066181715,0.00023866918,0.02098118],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99972576,0.000028028464,0.00004145682,0.000066598106,0.00009267419,0.000045386958],"domain_scores_gemma":[0.9996793,0.00007690498,0.000090875066,0.000057745197,0.000039460872,0.000055629593],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00017507655,0.00023979293,0.00020195202,0.0003647246,0.00034092416,0.00046090106,0.0004538508,0.00039813583,0.001930464],"category_scores_gemma":[0.00023200939,0.00022356809,0.00033532744,0.00020730474,0.00019803763,0.00019390378,0.0003357103,0.0008205246,0.0015420275],"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":[0.000020876765,0.000010882926,0.0003929525,0.000021133894,0.00000435079,0.00012530683,0.000026555259,0.000017532197,0.9981505,0.00018986616,0.00008156484,0.0009584903],"study_design_scores_gemma":[0.000012030808,0.00014874843,0.018014584,0.000013002415,0.000030306282,0.0014939343,0.000060146755,0.00041351747,0.968851,0.000059123304,0.010896854,0.000006833597],"about_ca_topic_score_codex":0.0017499818,"about_ca_topic_score_gemma":0.004677001,"teacher_disagreement_score":0.001930464,"about_ca_system_score_codex":0.0005359532,"about_ca_system_score_gemma":0.00024540132,"threshold_uncertainty_score":0.0064581037},"labels":[],"label_agreement":null},{"id":"W1996868983","doi":"10.1159/000095837","title":"Beckwith-Wiedemann Syndrome Presenting with an Elevated Triple Screen in the Second Trimester of Pregnancy","year":2006,"lang":"en","type":"article","venue":"Fetal Diagnosis and Therapy","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":23,"is_retracted":false,"has_abstract":true,"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":"Medicine; Beckwith–Wiedemann syndrome; Pregnancy; Obstetrics; Gynecology; Neonatology; Genetics","score_opus":0.013884707242240316,"score_gpt":0.24062652272720758,"score_spread":0.22674181548496727,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1996868983","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9948561,0.0005720585,0.0010172675,0.0004850802,0.000040554365,0.00002406018,0.000077654106,0.000062786676,0.0028644283],"genre_scores_gemma":[0.9983798,0.0003882877,0.0007331166,0.00010977024,0.000060246955,0.000010998374,0.00004584667,0.0000061731544,0.00026572976],"study_design_codex":"case_report","study_design_gemma":"case_report","domain_scores_codex":[0.99984,0.000030029796,0.000017133161,0.000033930617,0.00002863401,0.000050253246],"domain_scores_gemma":[0.99956805,0.00014108188,0.00013922273,0.000020803707,0.000013659378,0.000117232245],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00013900333,0.00092103204,0.00032646782,0.0008810993,0.00044563794,0.00039531657,0.0002506612,0.00096390455,0.0016637192],"category_scores_gemma":[0.0018319843,0.0003592856,0.00021567864,0.0004912803,0.0006462649,0.00038230245,0.0004901182,0.00057538855,0.00027324556],"study_design_candidate":"case_report","study_design_consensus":"case_report","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00017364895,0.000030330479,0.06192656,0.000025850964,0.000012876976,0.92492753,0.00028333103,0.00010514959,0.0067191147,0.00036013857,0.00054662884,0.004888957],"study_design_scores_gemma":[0.000021551838,0.000099459765,0.014488786,0.000010575665,0.000016333208,0.9829767,0.000095480005,0.00016554075,0.0015019086,0.00014982384,0.0004655079,0.000008465577],"about_ca_topic_score_codex":0.0010185572,"about_ca_topic_score_gemma":0.0014752932,"teacher_disagreement_score":0.0016637192,"about_ca_system_score_codex":0.0003053498,"about_ca_system_score_gemma":0.0003747779,"threshold_uncertainty_score":0.005565703},"labels":[],"label_agreement":null},{"id":"W1997094167","doi":"10.1016/j.modgep.2007.09.005","title":"The PcG gene Sfmbt2 is paternally expressed in extraembryonic tissues","year":2007,"lang":"en","type":"article","venue":"Gene Expression Patterns","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":63,"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 of Toronto","funders":"Eunice Kennedy Shriver National Institute of Child Health and Human Development; National Center for Research Resources","keywords":"Biology; Genomic imprinting; Genetics; Gene; Imprinting (psychology); Trophoblast; Embryo; CpG site; Placenta; DNA methylation; Gene expression; Fetus","score_opus":0.01176749455415954,"score_gpt":0.26196194538071566,"score_spread":0.2501944508265561,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1997094167","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9862955,0.002121814,0.007163185,0.00017500026,0.00005788203,0.000009869591,0.0008708675,0.00029063513,0.0030151724],"genre_scores_gemma":[0.99180555,0.0005654654,0.0016417851,0.00004400887,0.000022749236,0.000011703414,0.0010679205,0.0001068781,0.0047340314],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99979967,0.000017763103,0.000013785717,0.00006200181,0.00007062263,0.00003613117],"domain_scores_gemma":[0.99961346,0.0000791027,0.000107792745,0.00005328048,0.000037050122,0.0001093137],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00008603396,0.0005630084,0.00030345068,0.00096312835,0.00027064708,0.0004644979,0.00025390813,0.0004241853,0.0015486976],"category_scores_gemma":[0.00025900116,0.00043275728,0.0002401448,0.00045367522,0.0005273756,0.00023652495,0.0004272578,0.00065523095,0.00067029876],"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":[0.00008480962,0.0000029945168,0.0011498517,0.000014928143,0.0000063774123,0.00038542013,0.000019179672,0.000029214256,0.9966311,0.00015582608,0.00004436281,0.0014758413],"study_design_scores_gemma":[0.000028070086,0.000051722574,0.057578206,0.000008184698,0.00004221457,0.005613578,0.00004703415,0.0004881224,0.93213034,0.00021331443,0.0037879678,0.000011190656],"about_ca_topic_score_codex":0.0017701439,"about_ca_topic_score_gemma":0.0028988076,"teacher_disagreement_score":0.0017701439,"about_ca_system_score_codex":0.00032988528,"about_ca_system_score_gemma":0.00028787434,"threshold_uncertainty_score":0.005180955},"labels":[],"label_agreement":null},{"id":"W1997214852","doi":"10.1371/journal.pone.0008638","title":"The Imprinted Retrotransposon-Like Gene PEG11 (RTL1) Is Expressed as a Full-Length Protein in Skeletal Muscle from Callipyge Sheep","year":2010,"lang":"en","type":"article","venue":"PLoS ONE","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":42,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Simon Fraser University","funders":"Meat and Livestock Australia; Australian Wool Innovation; Utah State University","keywords":"Retrotransposon; Biology; Genetics; Gene; Genomic imprinting; Skeletal muscle; Gene expression; Phenotype; Regulation of gene expression; Genome; Molecular biology; Transposable element; DNA methylation; Anatomy","score_opus":0.01252471206177212,"score_gpt":0.2105023382397632,"score_spread":0.19797762617799108,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1997214852","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9958793,0.000924422,0.0016632838,0.00006588162,0.000014122414,0.0000089183695,0.00062211225,0.000072059316,0.00074976793],"genre_scores_gemma":[0.9891338,0.0006196472,0.0020721564,0.00006976728,0.000014013038,0.000021744674,0.0026561762,0.00003741068,0.005375293],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9999192,0.0000052605337,0.0000073715164,0.000033119333,0.000022191736,0.000012876754],"domain_scores_gemma":[0.99982846,0.000030599833,0.000074372525,0.000013855337,0.00000786876,0.000044857057],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00006558717,0.00027143242,0.0001935709,0.00036929766,0.00011471078,0.00024178126,0.00015465672,0.00030665385,0.0009538916],"category_scores_gemma":[0.00011228292,0.0001923067,0.00019103126,0.00018396587,0.00026339624,0.00014109496,0.0002648025,0.00034086435,0.00061171013],"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":[0.000032211472,0.0000028703885,0.00057135604,0.000017257367,0.0000031501486,0.00014199321,0.000013167095,0.0000119078495,0.9985415,0.000021661303,0.000014735143,0.00062827475],"study_design_scores_gemma":[0.000035276607,0.00022828362,0.13822526,0.000022171325,0.00006072033,0.005715239,0.00013906631,0.0010612956,0.8472547,0.00011021119,0.007131639,0.000016170381],"about_ca_topic_score_codex":0.00028415336,"about_ca_topic_score_gemma":0.00055055256,"teacher_disagreement_score":0.0009538916,"about_ca_system_score_codex":0.00021430908,"about_ca_system_score_gemma":0.00008082485,"threshold_uncertainty_score":0.0031910539},"labels":[],"label_agreement":null},{"id":"W1997905518","doi":"10.1006/bbrc.2001.5500","title":"Evidence against GRB10 as the Gene Responsible for Silver–Russell Syndrome","year":2001,"lang":"en","type":"article","venue":"Biochemical and Biophysical Research Communications","topic":"Genetic Syndromes and Imprinting","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 University Health Centre","funders":"","keywords":"Imprinting (psychology); Genomic imprinting; Gene; GRB10; Gene isoform; Biology; Genetics; Gene family; Gene expression; Endocrinology; Insulin; Insulin receptor; Insulin resistance","score_opus":0.11080214553273457,"score_gpt":0.3841055938591597,"score_spread":0.27330344832642517,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1997905518","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9739992,0.006932483,0.0045812526,0.0037847906,0.0005962804,0.000013854616,0.00024893245,0.0003437401,0.009499572],"genre_scores_gemma":[0.99293876,0.002337892,0.0021701395,0.00039625986,0.00016420135,0.0000075795924,0.00028952226,0.000022945911,0.001672703],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9998029,0.000032911463,0.00002588481,0.00003926861,0.0000572229,0.00004188561],"domain_scores_gemma":[0.9990095,0.00043595792,0.00015586449,0.00012340532,0.00010328585,0.00017198267],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0006405565,0.00067137444,0.00040669017,0.0010423065,0.00029319696,0.0005536294,0.001114408,0.00186001,0.0031254159],"category_scores_gemma":[0.0015006464,0.00028231414,0.00034113484,0.00044959824,0.00179651,0.0005164637,0.00051612465,0.0012527173,0.0010303962],"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":[0.00584894,0.00025665923,0.08856837,0.0006929608,0.00035442202,0.060270023,0.0004015274,0.0009600103,0.774211,0.022910884,0.005049052,0.040476166],"study_design_scores_gemma":[0.0014960255,0.0010336052,0.16120918,0.0003810187,0.0011145001,0.32950014,0.0012362974,0.007921214,0.3944244,0.029310549,0.07222402,0.00014913347],"about_ca_topic_score_codex":0.000645921,"about_ca_topic_score_gemma":0.00035821274,"teacher_disagreement_score":0.0031254159,"about_ca_system_score_codex":0.00026031496,"about_ca_system_score_gemma":0.000376007,"threshold_uncertainty_score":0.010455608},"labels":[],"label_agreement":null},{"id":"W1998116517","doi":"10.1002/1097-0223(200101)21:1<36::aid-pd979>3.0.co;2-1","title":"Two cases of confined placental mosaicism for chromosome 4, including one with maternal uniparental disomy","year":2001,"lang":"en","type":"article","venue":"Prenatal Diagnosis","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":34,"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 Research (Canada)","funders":"","keywords":"Uniparental disomy; Trisomy; Aneuploidy; Chorionic villus sampling; Biology; Chorionic villi; Placenta; Chromosome; Genetics; Andrology; Fetus; Nondisjunction; Karyotype; Pregnancy; Prenatal diagnosis; Medicine; Gene","score_opus":0.023843175649213975,"score_gpt":0.27039333692654727,"score_spread":0.24655016127733329,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1998116517","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9890933,0.002919499,0.0032705695,0.00048507372,0.000107910935,0.0001499666,0.00018594356,0.00014573529,0.0036421109],"genre_scores_gemma":[0.9963469,0.0008410754,0.0014950233,0.00015319837,0.00013268764,0.00004998778,0.00009735523,0.000020630661,0.0008631601],"study_design_codex":"case_report","study_design_gemma":"case_report","domain_scores_codex":[0.9993593,0.000094587376,0.0000644956,0.00014716297,0.000085892876,0.00024858525],"domain_scores_gemma":[0.997703,0.00076569413,0.000668279,0.00032851097,0.00006846023,0.00046599057],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00035567489,0.0023087722,0.00086010125,0.0026596792,0.0013272674,0.0009016791,0.0011845247,0.0025169847,0.0017869438],"category_scores_gemma":[0.0060442127,0.0016829009,0.0006583918,0.0014531056,0.0026172902,0.0005260695,0.0020854997,0.0014775054,0.000497432],"study_design_candidate":"case_report","study_design_consensus":"case_report","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00018392262,0.00006113563,0.025483968,0.00006649812,0.000042854314,0.96458465,0.00046000723,0.000097651886,0.0026427333,0.00032214416,0.00038366308,0.005670751],"study_design_scores_gemma":[0.00003722581,0.00018232422,0.012794574,0.000009266218,0.000024658739,0.9849407,0.00008698562,0.000068543544,0.0009812639,0.000232725,0.0006266409,0.0000150431115],"about_ca_topic_score_codex":0.0021398603,"about_ca_topic_score_gemma":0.0027219884,"teacher_disagreement_score":0.0026596792,"about_ca_system_score_codex":0.0007682575,"about_ca_system_score_gemma":0.0004786608,"threshold_uncertainty_score":0.0059779286},"labels":[],"label_agreement":null},{"id":"W1998591794","doi":"10.1002/(sici)1097-0215(20000601)86:5<690::aid-ijc14>3.0.co;2-k","title":"ARHI is the center of allelic deletion on chromosome 1p31 in ovarian and breast cancers","year":2000,"lang":"en","type":"article","venue":"International Journal of Cancer","topic":"Genetic Syndromes and Imprinting","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","funders":"National Cancer Institute; Ovarian Cancer Research Fund","keywords":"Loss of heterozygosity; Cancer research; Biology; Ovarian cancer; Tumor suppressor gene; Breast cancer; Allele; Cancer; Genetics; Gene; Carcinogenesis","score_opus":0.006103453788862071,"score_gpt":0.2647152003580528,"score_spread":0.2586117465691907,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1998591794","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99238867,0.0026096243,0.0024471062,0.000084468404,0.000010640658,0.000027827431,0.00031766485,0.000079540136,0.0020344262],"genre_scores_gemma":[0.9971731,0.00056440535,0.0012366151,0.000023610104,0.000007577591,0.0000133835565,0.00038621746,0.00000645404,0.0005886289],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9998248,0.000025495829,0.000013988907,0.000056369976,0.000044882996,0.00003445867],"domain_scores_gemma":[0.99980205,0.000044331933,0.000078753794,0.000026259038,0.0000130143,0.00003561648],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00015443287,0.00018628153,0.00025251947,0.000738921,0.0002540929,0.00024750078,0.0003047754,0.00020532597,0.0012590848],"category_scores_gemma":[0.00030818084,0.00018585572,0.00017732887,0.00043423957,0.00026754403,0.00011697265,0.00033437772,0.0002601393,0.00044050193],"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":[0.00071179774,0.000042641885,0.04697128,0.00015238496,0.0000528688,0.004412238,0.00019317756,0.00037874197,0.92119235,0.0007029406,0.00028345612,0.024906134],"study_design_scores_gemma":[0.0000834067,0.0005121671,0.62772,0.00003682033,0.00014061351,0.040042497,0.00019692356,0.0010772353,0.31442088,0.0010050086,0.014731576,0.00003289997],"about_ca_topic_score_codex":0.0005304764,"about_ca_topic_score_gemma":0.00066377356,"teacher_disagreement_score":0.0012590848,"about_ca_system_score_codex":0.00015927537,"about_ca_system_score_gemma":0.00016196254,"threshold_uncertainty_score":0.0042120814},"labels":[],"label_agreement":null},{"id":"W1999357871","doi":"10.1111/j.1541-0420.2006.00610.x","title":"Quantifying Genomic Imprinting in the Presence of Linkage","year":2006,"lang":"en","type":"article","venue":"Biometrics","topic":"Genetic Syndromes and Imprinting","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":"McGill University","funders":"","keywords":"Imprinting (psychology); Genomic imprinting; Genetic linkage; Genetics; Biology; Computational biology; Gene","score_opus":0.029310173032650415,"score_gpt":0.2739906408264836,"score_spread":0.2446804677938332,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1999357871","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":[0.38182575,0.00089121354,0.6139149,0.00021164562,0.00003107145,0.00004100066,0.00024382611,0.00031588503,0.0025247617],"genre_scores_gemma":[0.954745,0.0002601768,0.044472046,0.000046806796,0.000016158958,0.000041046147,0.00013918971,0.000024808955,0.00025470715],"study_design_codex":"design_other","study_design_gemma":"theoretical_or_conceptual","domain_scores_codex":[0.9954555,0.0027323666,0.00017010082,0.00073551555,0.00069913303,0.00020734133],"domain_scores_gemma":[0.96395975,0.030333437,0.0019611549,0.0029123763,0.00054642395,0.0002869449],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.008257004,0.00056593097,0.00088301266,0.0015634475,0.0003445085,0.0011579181,0.0008769183,0.0007314504,0.0015235976],"category_scores_gemma":[0.04068325,0.00036470772,0.00052295404,0.0010748345,0.0024048313,0.0019362009,0.0021858998,0.00085384544,0.00015072283],"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":[0.000902416,0.0001547759,0.21853814,0.00094015076,0.0012763712,0.0015353,0.0009334712,0.23041084,0.15280066,0.10536015,0.00055066636,0.2865971],"study_design_scores_gemma":[0.00008258929,0.0007185278,0.1724554,0.00010585477,0.0004102852,0.0025108256,0.00033976455,0.4652827,0.09618353,0.2591209,0.00253856,0.00025100342],"about_ca_topic_score_codex":0.00053415546,"about_ca_topic_score_gemma":0.0005436533,"teacher_disagreement_score":0.008257004,"about_ca_system_score_codex":0.00037369248,"about_ca_system_score_gemma":0.00037754053,"threshold_uncertainty_score":0.043667734},"labels":[],"label_agreement":null},{"id":"W2000287799","doi":"10.1002/jnr.20493","title":"Mice with the deleted neurofilament of low molecular weight (Nefl) gene: 2. Effects on motor functions and spatial orientation","year":2005,"lang":"en","type":"article","venue":"Journal of Neuroscience Research","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":32,"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; Hôpital Saint-Luc; Montreal General Hospital","funders":"","keywords":"Cerebellum; Brainstem; Morris water navigation task; Ataxia; Neuroscience; Neurofilament; Open field; Water maze; Biology; Psychology; Internal medicine; Endocrinology; Medicine; Hippocampal formation","score_opus":0.015502149338215719,"score_gpt":0.29861235707100503,"score_spread":0.28311020773278933,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2000287799","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9959079,0.00021462036,0.0011778157,0.000084758176,0.000031278567,0.00004202201,0.001506126,0.0001550428,0.000880398],"genre_scores_gemma":[0.9726795,0.0005704451,0.004041423,0.000094150775,0.000043560274,0.00018590086,0.003708654,0.00024833545,0.018427985],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9997434,0.000026418225,0.000041754185,0.000079732476,0.000050285875,0.0000584682],"domain_scores_gemma":[0.99919146,0.00011069303,0.00032139051,0.000041360443,0.000037716763,0.00029738765],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00023142919,0.0014575697,0.00044667843,0.001414236,0.00030855124,0.00034745512,0.00047357797,0.0009615266,0.0063786367],"category_scores_gemma":[0.0002543542,0.0003635927,0.00043965093,0.0003169931,0.00085452636,0.00039567964,0.00037102855,0.0009426088,0.00096427236],"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":[0.0010766647,0.00032440908,0.0009800749,0.000042038366,0.00002450456,0.00059960876,0.0000495018,0.00007977784,0.99536383,0.0001690226,0.000092594586,0.0011979539],"study_design_scores_gemma":[0.00065300916,0.003128801,0.033532497,0.000056228168,0.00018207802,0.006822745,0.00022590347,0.0017222262,0.94880766,0.00025767853,0.004555345,0.00005575906],"about_ca_topic_score_codex":0.0015433802,"about_ca_topic_score_gemma":0.0018070457,"teacher_disagreement_score":0.0063786367,"about_ca_system_score_codex":0.00045416004,"about_ca_system_score_gemma":0.00020513046,"threshold_uncertainty_score":0.021338701},"labels":[],"label_agreement":null},{"id":"W2000472408","doi":"10.1354/vp.45-5-663","title":"Laboratory Findings, Histopathology, and Immunophenotype of Lymphoma in Domestic Ferrets","year":2008,"lang":"en","type":"article","venue":"Veterinary Pathology","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":54,"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 Guelph","funders":"University of Guelph; University of Saskatchewan","keywords":"Lymphoma; Pathology; Immunophenotyping; Medicine; Histopathology; Anaplastic large-cell lymphoma; T-cell lymphoma; Immunology","score_opus":0.01577691926152182,"score_gpt":0.24810112811157575,"score_spread":0.23232420885005395,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2000472408","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9995165,0.00013244747,0.00008619269,0.000009310614,0.000002360242,0.0000035394485,0.000031647225,0.0000043999225,0.00021367022],"genre_scores_gemma":[0.99955827,0.00008185532,0.00015099887,0.000014435818,0.0000055113337,0.000008345438,0.00008224415,0.000001697938,0.000096740885],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99977547,0.000042230364,0.000027686026,0.00007183798,0.00004357501,0.000039215214],"domain_scores_gemma":[0.99947137,0.0001406938,0.00020724915,0.000032172607,0.000061103034,0.000087424865],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00038385802,0.00034232234,0.00027409932,0.0013305462,0.0002704322,0.0003066746,0.00019133058,0.00032714862,0.00042106063],"category_scores_gemma":[0.0014199433,0.00016484494,0.0001873126,0.00019828626,0.0005393567,0.00051318645,0.00019882545,0.00018195168,0.0001322601],"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":[0.0002902063,0.000093922754,0.95046765,0.000028767028,0.00003562146,0.0047395895,0.00028676377,0.0001370652,0.03951693,0.000036104033,0.000112411035,0.0042550126],"study_design_scores_gemma":[0.000009193925,0.0004922682,0.9853129,0.000009358635,0.00003101601,0.009695842,0.0003764521,0.00025679,0.0035118135,0.00005293767,0.0002420592,0.000009375966],"about_ca_topic_score_codex":0.0010942812,"about_ca_topic_score_gemma":0.0010729209,"teacher_disagreement_score":0.0013305462,"about_ca_system_score_codex":0.00042816193,"about_ca_system_score_gemma":0.0000871142,"threshold_uncertainty_score":0.0031064749},"labels":[],"label_agreement":null},{"id":"W2001481979","doi":"10.1186/1471-213x-9-9","title":"In vitroculture and somatic cell nuclear transfer affect imprinting of SNRPN gene in pre- and post-implantation stages of development in cattle","year":2009,"lang":"en","type":"article","venue":"BMC Developmental Biology","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":86,"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; Cegep de Saint Hyacinthe","funders":"Institute of Human Development, Child and Youth Health; Natural Sciences and Engineering Research Council of Canada; Canadian Institutes of Health Research; Conselho Nacional de Desenvolvimento Científico e Tecnológico","keywords":"Genomic imprinting; Biology; Somatic cell nuclear transfer; Imprinting (psychology); Reprogramming; DNA methylation; Epigenetics; Methylation; Genetics; Somatic cell; Embryo; Andrology; Molecular biology; Gene expression; Gene; Blastocyst; Embryogenesis","score_opus":0.005892786256505913,"score_gpt":0.22557095788970113,"score_spread":0.21967817163319522,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2001481979","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9977215,0.00096767966,0.000609455,0.000019919251,0.0000116535075,0.00000749375,0.00013644947,0.0000067387145,0.00051916257],"genre_scores_gemma":[0.99598384,0.0009885194,0.000610646,0.000035182864,0.000010118412,0.000027165623,0.00047490263,0.000009781377,0.0018598678],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9997787,0.00004464324,0.000017585515,0.00005156146,0.000048985432,0.000058452086],"domain_scores_gemma":[0.99976426,0.000081701764,0.00007908438,0.000014437044,0.000014469974,0.00004603607],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00020939637,0.0002261886,0.00020630538,0.0002321012,0.00018247897,0.0002625433,0.00020345899,0.00025106157,0.0011453338],"category_scores_gemma":[0.00029297257,0.00010978273,0.00018662482,0.00015499789,0.00024748474,0.00013869735,0.0001838922,0.00030130154,0.00018835369],"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":[0.00029562347,0.000042571704,0.0039599314,0.000035940408,0.00001255739,0.00010050268,0.00008779008,0.000054468845,0.9935881,0.0000379774,0.000019795114,0.0017647612],"study_design_scores_gemma":[0.00001956133,0.001670764,0.14585382,0.000019159941,0.0000841614,0.00058489,0.00028911937,0.00057230843,0.8480727,0.000067376204,0.0027547346,0.00001145196],"about_ca_topic_score_codex":0.0020711343,"about_ca_topic_score_gemma":0.0025473055,"teacher_disagreement_score":0.0020711343,"about_ca_system_score_codex":0.0003928319,"about_ca_system_score_gemma":0.00017280258,"threshold_uncertainty_score":0.0041181445},"labels":[],"label_agreement":null},{"id":"W2001973648","doi":"10.1210/jc.2011-2406","title":"Muscle-Bone Characteristics in Children with Prader-Willi Syndrome","year":2011,"lang":"en","type":"article","venue":"The Journal of Clinical Endocrinology & Metabolism","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":27,"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; McGill University","funders":"Canadian Institutes of Health Research","keywords":"Endocrinology; Short stature; Internal medicine; Medicine; Bone mineral; Lumbar spine; Bone density; Osteoporosis; Surgery","score_opus":0.03494359590288171,"score_gpt":0.2962059595211334,"score_spread":0.26126236361825167,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2001973648","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9996495,0.00009309398,0.000042492997,0.0000128931615,0.000001803619,0.000004694187,0.00009890919,0.000003231573,0.000093253126],"genre_scores_gemma":[0.9992569,0.00014772324,0.00019787038,0.00001526706,0.0000071360514,0.000012919526,0.00027910052,0.0000026348482,0.0000804268],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9997614,0.000044537344,0.000030448162,0.000057609122,0.00006654353,0.000039550352],"domain_scores_gemma":[0.9994092,0.00014336448,0.00027402185,0.000019333342,0.000047485893,0.00010652135],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00028913,0.00060872186,0.00044942144,0.0014515843,0.00031884166,0.0003079221,0.00023483626,0.0003681403,0.0015852065],"category_scores_gemma":[0.001430876,0.00026593625,0.0002303898,0.0006867233,0.0004586138,0.00029686818,0.00039550674,0.00031764986,0.00020229969],"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":[0.00011764475,0.000029928498,0.99385923,0.000021168149,0.00002736743,0.0016835432,0.00014598879,0.00006741932,0.002009982,0.000021290718,0.000074144984,0.001942369],"study_design_scores_gemma":[0.000013730437,0.00031689674,0.99001443,0.000007881209,0.000020457725,0.008928012,0.00020225778,0.00010298182,0.00021218602,0.000021322065,0.00015604102,0.0000037746101],"about_ca_topic_score_codex":0.0020509104,"about_ca_topic_score_gemma":0.0019411674,"teacher_disagreement_score":0.0020509104,"about_ca_system_score_codex":0.00018414346,"about_ca_system_score_gemma":0.0002076636,"threshold_uncertainty_score":0.005303085},"labels":[],"label_agreement":null},{"id":"W2002012888","doi":"10.1111/j.1399-0004.2010.01615.x","title":"19p13.2 microduplication causes a Sotos syndrome‐like phenotype and alters gene expression","year":2010,"lang":"en","type":"article","venue":"Clinical Genetics","topic":"Genetic Syndromes and Imprinting","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":"Children's Hospital of Eastern Ontario; University of British Columbia","funders":"Javna Agencija za Raziskovalno Dejavnost RS","keywords":"Sotos syndrome; Gene duplication; Genetics; Haploinsufficiency; Biology; Gene; Copy-number variation; Macrocephaly; Pseudogene; Phenotype; Genome","score_opus":0.02157716342541003,"score_gpt":0.31028473006809004,"score_spread":0.28870756664268,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2002012888","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99825627,0.00020559835,0.0005910369,0.000032240714,0.000004754286,0.00001001319,0.00016349576,0.000049050042,0.00068751496],"genre_scores_gemma":[0.99822766,0.00024264227,0.0006989087,0.000016642582,0.000009989773,0.000010324572,0.00018867862,0.000013600208,0.0005915845],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9998319,0.000024183933,0.000012683775,0.000046581707,0.000059071983,0.000025564037],"domain_scores_gemma":[0.9997973,0.00004034325,0.00009246717,0.000012268938,0.000009987293,0.00004757447],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00006790798,0.0008458945,0.0002966113,0.000909952,0.00018966605,0.00015232498,0.00015154613,0.00031661557,0.0018188562],"category_scores_gemma":[0.00032648185,0.00020162878,0.00017739042,0.00040146342,0.00038430453,0.00007883262,0.00030095386,0.00020874233,0.00021905534],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0005897223,0.000067095265,0.05018237,0.00007257828,0.00010313556,0.039371308,0.00013879596,0.00030111335,0.895001,0.00048375074,0.00032417147,0.013365037],"study_design_scores_gemma":[0.00010623844,0.0009448452,0.47471654,0.00003273899,0.00020264294,0.30137274,0.00015175708,0.001575521,0.215606,0.00064057024,0.0046210573,0.000029365856],"about_ca_topic_score_codex":0.00062783546,"about_ca_topic_score_gemma":0.0009953527,"teacher_disagreement_score":0.0018188562,"about_ca_system_score_codex":0.00016205276,"about_ca_system_score_gemma":0.00014374002,"threshold_uncertainty_score":0.00608474},"labels":[],"label_agreement":null},{"id":"W2002733724","doi":"10.1002/ajmg.a.37058","title":"Mild Angelman syndrome phenotype due to a mosaic methylation imprinting defect","year":2015,"lang":"en","type":"article","venue":"American Journal of Medical Genetics Part A","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":20,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Library of Parliament; Hospital for Sick Children; University of Toronto","funders":"Bundesministerium für Bildung und Forschung","keywords":"Imprinting (psychology); Angelman syndrome; Genomic imprinting; Phenotype; Genetics; Mosaic; Methylation; DNA methylation; Biology; DNA; Gene; History","score_opus":0.021693031545645825,"score_gpt":0.29237799957478466,"score_spread":0.27068496802913883,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2002733724","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9928671,0.0005598526,0.0017147204,0.00035029798,0.00004890594,0.000024371982,0.0004175301,0.00014092629,0.0038764195],"genre_scores_gemma":[0.99793756,0.0002499944,0.00068677263,0.000055186752,0.00002195929,0.0000046779137,0.00008414518,0.000010058078,0.00094967603],"study_design_codex":"case_report","study_design_gemma":"case_report","domain_scores_codex":[0.9999355,0.000008983459,0.0000062651584,0.000020970057,0.00001566062,0.000012594634],"domain_scores_gemma":[0.9997745,0.000068446636,0.00008757606,0.000009961202,0.000010303636,0.00004919032],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00006931821,0.00055402634,0.00021825307,0.00034185383,0.00015831314,0.00013680004,0.00016787558,0.0002808837,0.0021419646],"category_scores_gemma":[0.0005724691,0.00010230317,0.00015588036,0.00014034274,0.00037253628,0.00021697932,0.00026250325,0.00023517305,0.00027396812],"study_design_candidate":"case_report","study_design_consensus":"case_report","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.000346517,0.000042418247,0.0721662,0.00017322255,0.000056480392,0.78211385,0.0005243269,0.00040322455,0.12864342,0.002946906,0.0010390717,0.011544427],"study_design_scores_gemma":[0.000049422517,0.00034418004,0.10174013,0.000035881174,0.00006536146,0.87213445,0.00021585079,0.0008600697,0.018961644,0.0014858003,0.0040755738,0.000031575644],"about_ca_topic_score_codex":0.0011693421,"about_ca_topic_score_gemma":0.0017650157,"teacher_disagreement_score":0.0021419646,"about_ca_system_score_codex":0.00018693008,"about_ca_system_score_gemma":0.00023626104,"threshold_uncertainty_score":0.007165551},"labels":[],"label_agreement":null},{"id":"W2004543571","doi":"10.1359/jbmr.090825","title":"Parathyroid hormone regulates fetal-placental mineral homeostasis","year":2009,"lang":"en","type":"article","venue":"Journal of Bone and Mineral Research","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":91,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Jewish General Hospital; McGill University; Memorial University of Newfoundland","funders":"Canadian Institutes of Health Research; American Society for Bone and Mineral Research; Canadian Diabetes Association","keywords":"Endocrinology; Internal medicine; Parathyroid hormone; Homeostasis; Fetus; Calcium metabolism; Placenta; Hypoparathyroidism; Calcium; Parathyroid chief cell; Hyperphosphatemia; Biology; Calcium-sensing receptor; Medicine; Pregnancy","score_opus":0.026351582055128553,"score_gpt":0.31806359985978394,"score_spread":0.2917120178046554,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2004543571","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.94586253,0.021824162,0.01770409,0.00075919484,0.00009384479,0.00003245571,0.0005600536,0.0003772293,0.012786441],"genre_scores_gemma":[0.9915139,0.0039988863,0.0023408083,0.000048636444,0.000017774488,0.000009096701,0.00013132002,0.00002618555,0.0019134532],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9998747,0.000020324826,0.0000073088677,0.000025072975,0.000048529593,0.000024134484],"domain_scores_gemma":[0.99983513,0.00003509275,0.00004459946,0.000015573145,0.0000256571,0.000043988643],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00013190342,0.00019883929,0.00016314813,0.00031072245,0.00014285556,0.00038772315,0.00029697266,0.00026282878,0.0012921811],"category_scores_gemma":[0.00032947923,0.00013386706,0.00009297111,0.00015025733,0.00032915926,0.0002301321,0.00031290564,0.00033415304,0.0004150977],"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":[0.00015057491,0.000008208087,0.0026006717,0.000058564376,0.0000063456214,0.00045448268,0.000051740488,0.00012382766,0.98345333,0.0016245977,0.00015859395,0.011309162],"study_design_scores_gemma":[0.00007895379,0.0002723024,0.09427655,0.000050549075,0.00006634464,0.006104376,0.00020574035,0.0015597832,0.8654311,0.0037417647,0.02818518,0.0000273615],"about_ca_topic_score_codex":0.00055361015,"about_ca_topic_score_gemma":0.00053011294,"teacher_disagreement_score":0.0012921811,"about_ca_system_score_codex":0.00038955186,"about_ca_system_score_gemma":0.00023692085,"threshold_uncertainty_score":0.0043227077},"labels":[],"label_agreement":null},{"id":"W2004708536","doi":"10.1074/jbc.m110.170704","title":"Phosphatidylinositol 3-Kinase (PI3K) Signaling via Glycogen Synthase Kinase-3 (Gsk-3) Regulates DNA Methylation of Imprinted Loci","year":2010,"lang":"en","type":"article","venue":"Journal of Biological Chemistry","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":91,"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","funders":"National Center for Advancing Translational Sciences; National Center for Research Resources; National Institute of Diabetes and Digestive and Kidney Diseases; National Institutes of Health; National Cancer Institute; National Institute on Aging","keywords":"GSK-3; Biology; DNA methylation; Glycogen synthase; Signal transduction; Molecular biology; Cell biology; Biochemistry; Phosphorylation; Gene; Gene expression","score_opus":0.011350909381504794,"score_gpt":0.24519431364529648,"score_spread":0.2338434042637917,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2004708536","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9768414,0.0045685642,0.014168594,0.00033754655,0.000046696336,0.000028021046,0.0005570908,0.00027500003,0.003177015],"genre_scores_gemma":[0.9939464,0.0022924172,0.0022891776,0.000036838068,0.0000054526718,0.00001516659,0.00018776265,0.000010411456,0.0012164514],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99995995,0.000006497669,0.0000030634328,0.000009073804,0.000010612906,0.000010783077],"domain_scores_gemma":[0.99997175,0.000004397324,0.000010332397,0.0000032648668,0.0000024082851,0.000007813969],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00007343088,0.00030819786,0.000095245014,0.00019410874,0.00009967973,0.00022692996,0.00011152976,0.00013199906,0.0007942931],"category_scores_gemma":[0.00009610928,0.00009266063,0.00017248075,0.0001378522,0.00024849127,0.00013272541,0.00019009586,0.0003329177,0.00026482574],"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":[0.000059559898,0.0000058738174,0.00058701826,0.000023149216,0.000004660649,0.00006218326,0.000006479032,0.00009935008,0.99633515,0.00025619727,0.00003460498,0.0025258723],"study_design_scores_gemma":[0.000016947717,0.000074830765,0.009225724,0.0000058756937,0.00001946127,0.0002953476,0.00001450543,0.0008064546,0.98724085,0.00037366923,0.0019225372,0.00000388546],"about_ca_topic_score_codex":0.00047408,"about_ca_topic_score_gemma":0.0013118621,"teacher_disagreement_score":0.0007942931,"about_ca_system_score_codex":0.0003185755,"about_ca_system_score_gemma":0.00028461698,"threshold_uncertainty_score":0.002657175},"labels":[],"label_agreement":null},{"id":"W2005611432","doi":"10.1038/ejhg.2013.132","title":"Clinical utility gene card for: Beckwith–Wiedemann Syndrome","year":2013,"lang":"en","type":"article","venue":"European Journal of Human Genetics","topic":"Genetic Syndromes and Imprinting","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":"SickKids Foundation; Hospital for Sick Children; University of Toronto","funders":"National Institute of General Medical Sciences; Instituto de Salud Carlos III; Agence Nationale de la Recherche; Assistance publique-Hôpitaux de Paris; Bundesministerium für Bildung und Forschung; Institut National de la Santé et de la Recherche Médicale; Action Medical Research","keywords":"Beckwith–Wiedemann syndrome; Genetics; Gene; Medicine; Biology; Computational biology; Gene expression","score_opus":0.038195041901473,"score_gpt":0.3009586668574965,"score_spread":0.2627636249560235,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2005611432","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":[0.7835254,0.017822891,0.019325843,0.027092531,0.0030753512,0.00042266306,0.004401357,0.00162482,0.14270918],"genre_scores_gemma":[0.969906,0.003986117,0.011536204,0.0019572503,0.00078918115,0.00005951127,0.0014081509,0.00015150399,0.010206026],"study_design_codex":"case_report","study_design_gemma":"not_applicable","domain_scores_codex":[0.99967897,0.00006293967,0.000040270206,0.00007895728,0.00008781976,0.000051021358],"domain_scores_gemma":[0.999143,0.00031501203,0.00007918205,0.000075665936,0.00017762283,0.00020950513],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00034517125,0.0010273067,0.0004717476,0.00215232,0.00042741076,0.0010515908,0.0005548029,0.0017019794,0.012948313],"category_scores_gemma":[0.003443426,0.0001758542,0.00029090652,0.00066421274,0.00050899806,0.000661356,0.00055800955,0.000697229,0.0033931648],"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":[0.0009871627,0.00020534972,0.21925169,0.0003900582,0.000071425035,0.4093483,0.00039284088,0.00069711445,0.042663477,0.0071991547,0.045463093,0.27333036],"study_design_scores_gemma":[0.0001454153,0.0002658986,0.11065464,0.00048054667,0.0001647163,0.7639507,0.0006434836,0.003425136,0.023918437,0.010215289,0.08604719,0.00008857976],"about_ca_topic_score_codex":0.0010602524,"about_ca_topic_score_gemma":0.00088811206,"teacher_disagreement_score":0.012948313,"about_ca_system_score_codex":0.00033777923,"about_ca_system_score_gemma":0.0007117243,"threshold_uncertainty_score":0.043316364},"labels":[],"label_agreement":null},{"id":"W2006583840","doi":"10.1007/s00439-007-0440-1","title":"A genome-wide approach to identifying novel-imprinted genes","year":2007,"lang":"en","type":"article","venue":"Human Genetics","topic":"Genetic Syndromes and Imprinting","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":"Ontario Institute for Cancer Research; McGill University and Génome Québec Innovation Centre","funders":"","keywords":"Genomic imprinting; Biology; Genetics; Gene; Imprinting (psychology); Genome; Candidate gene; Allele; Genotyping; Human genome; DNA microarray; Computational biology; Gene expression; Genotype; DNA methylation","score_opus":0.03568799286872105,"score_gpt":0.28333428553889034,"score_spread":0.2476462926701693,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2006583840","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.73832643,0.008674748,0.22903387,0.001057813,0.00021345177,0.0006117191,0.0120595135,0.0009756621,0.0090468405],"genre_scores_gemma":[0.8567374,0.0026695863,0.12758182,0.0011433162,0.00012920798,0.0004195235,0.006905875,0.00017231156,0.0042409427],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99951935,0.00014494496,0.00002020127,0.00018807499,0.00008513663,0.000042171177],"domain_scores_gemma":[0.99954516,0.00023693877,0.00005082267,0.00006063726,0.000054322554,0.000052018764],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0011352273,0.0005791484,0.00084475346,0.0018052352,0.00054937444,0.0007449708,0.0006282568,0.0006292348,0.0019253993],"category_scores_gemma":[0.0010384202,0.00027465046,0.0010410963,0.0011350822,0.00031673242,0.00019635126,0.0006866169,0.0009011217,0.0003727434],"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":[0.00083799264,0.00017647269,0.030212788,0.00033115843,0.0013899568,0.000691343,0.00013775029,0.002389932,0.90461373,0.0016867381,0.0014376309,0.056094516],"study_design_scores_gemma":[0.00048743963,0.0015188378,0.5694991,0.000053311185,0.003415272,0.0071566934,0.000341557,0.022103261,0.34728917,0.005800995,0.04218882,0.00014560498],"about_ca_topic_score_codex":0.0021563023,"about_ca_topic_score_gemma":0.0070192665,"teacher_disagreement_score":0.0021563023,"about_ca_system_score_codex":0.00026707433,"about_ca_system_score_gemma":0.0004486696,"threshold_uncertainty_score":0.0064411163},"labels":[],"label_agreement":null},{"id":"W2007318061","doi":"10.1002/ajmg.a.33251","title":"Review and hypothesis: Syndromes with severe intrauterine growth restriction and very short stature—Are they related to the epigenetic mechanism(s) of fetal survival involved in the developmental origins of adult health and disease?","year":2010,"lang":"en","type":"review","venue":"American Journal of Medical Genetics Part A","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":37,"is_retracted":false,"has_abstract":true,"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":"","keywords":"Epigenetics; Intrauterine growth restriction; Fetus; DNA methylation; Mechanism (biology); Biology; Disease; Epigenesis; Short stature; Genomic imprinting; Genetics; Phenotype; Natural history; Bioinformatics; Physiology; Pregnancy; Medicine; Endocrinology; Gene; Internal medicine; Gene expression","score_opus":0.020407634992451497,"score_gpt":0.28533117824163123,"score_spread":0.2649235432491797,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2007318061","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":[0.00009664246,0.9939826,0.00015319003,0.0013537635,0.00237662,0.000010826182,0.00003690461,0.000015483376,0.0019739575],"genre_scores_gemma":[0.0006029664,0.99470985,0.00025906975,0.001271167,0.0017564553,0.000016939593,0.00006325654,0.000003288757,0.0013169766],"study_design_codex":"design_other","study_design_gemma":"theoretical_or_conceptual","domain_scores_codex":[0.9998149,0.000038772698,0.00003152051,0.000036701345,0.000063443695,0.000014773266],"domain_scores_gemma":[0.99951863,0.00021437772,0.000078462755,0.000013002449,0.00010117219,0.0000742728],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0004841411,0.0013129245,0.0018370899,0.0024841619,0.00036335376,0.0011296398,0.0015905738,0.0016785358,0.007196526],"category_scores_gemma":[0.0013535823,0.00028125054,0.00039357276,0.003330299,0.001070769,0.002972649,0.0007957197,0.0022578912,0.0054758224],"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":[0.00010486549,0.00006119871,0.00032815125,0.015943283,0.00009396801,0.00080630794,0.000089183835,0.00030000947,0.00088959024,0.004209993,0.30799368,0.66917974],"study_design_scores_gemma":[0.000026931964,0.000041813768,0.0010192253,0.0031773264,0.00006525661,0.004667734,0.00008836287,0.00004846958,0.000093472394,0.002198879,0.98855525,0.00001728678],"about_ca_topic_score_codex":0.00092937215,"about_ca_topic_score_gemma":0.0015939516,"teacher_disagreement_score":0.007196526,"about_ca_system_score_codex":0.00073635625,"about_ca_system_score_gemma":0.0012442642,"threshold_uncertainty_score":0.024074733},"labels":[],"label_agreement":null},{"id":"W2007808077","doi":"10.1006/dbio.2000.9839","title":"Activation of Fgf4 Gene Expression in the Myotomes Is Regulated by Myogenic bHLH Factors and by Sonic Hedgehog","year":2000,"lang":"en","type":"article","venue":"Developmental Biology","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","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":"McMaster University","funders":"National Cancer Institute","keywords":"MYF5; MyoD; Myotome; Biology; Enhancer; Limb bud; Sonic hedgehog; Cell biology; PITX2; Apical ectodermal ridge; Myogenesis; Genetics; Mesoderm; Gene expression; Myocyte; Homeobox; Somite; Gene; Embryonic stem cell; Signal transduction; Embryo; Embryogenesis","score_opus":0.007355290269801694,"score_gpt":0.22264130273161137,"score_spread":0.21528601246180967,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2007808077","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9858084,0.0025780532,0.003991726,0.00015780416,0.000044356122,0.000026142225,0.00041773124,0.00010405181,0.0068718134],"genre_scores_gemma":[0.98059505,0.0008514191,0.002684745,0.000054705473,0.000026731102,0.00005226952,0.0007555337,0.00006410104,0.014915429],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9997639,0.000047325808,0.00001453238,0.000028146593,0.00006289173,0.00008313967],"domain_scores_gemma":[0.9998129,0.000043156044,0.000032590902,0.000021142945,0.00003525772,0.000054972577],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00018275095,0.00037975077,0.00028244307,0.00066093955,0.00043108873,0.0004851193,0.0003092513,0.00030612922,0.0022542912],"category_scores_gemma":[0.00025062126,0.00041927682,0.00035775284,0.00021613791,0.00045966485,0.0003366298,0.0005775625,0.00047193648,0.0008436864],"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":[0.00020758073,0.0000035327441,0.00027785928,0.000015414758,0.0000038972717,0.00007935969,0.000014013109,0.000024813082,0.99832183,0.00025020397,0.000030546034,0.0007709717],"study_design_scores_gemma":[0.000017475677,0.000059978105,0.016189333,0.000004925167,0.000009410344,0.00028567412,0.000056414003,0.000481472,0.98056006,0.00013913034,0.0021907256,0.0000053217555],"about_ca_topic_score_codex":0.0029284758,"about_ca_topic_score_gemma":0.005567311,"teacher_disagreement_score":0.0029284758,"about_ca_system_score_codex":0.0009039518,"about_ca_system_score_gemma":0.00034080946,"threshold_uncertainty_score":0.007541299},"labels":[],"label_agreement":null},{"id":"W2008346671","doi":"10.1006/geno.2001.6502","title":"Maternal and Paternal Chromosomes 7 Show Differential Methylation of Many Genes in Lymphoblast DNA","year":2001,"lang":"en","type":"article","venue":"Genomics","topic":"Genetic Syndromes and Imprinting","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":"University of Toronto; Hospital for Sick Children","funders":"","keywords":"Biology; Genomic imprinting; DNA methylation; Methylation; Genetics; Gene; Imprinting (psychology); Lymphoblast; Uniparental disomy; Chromosome; Molecular biology; Gene expression; Karyotype; Cell culture","score_opus":0.008352606942159734,"score_gpt":0.21516008379199053,"score_spread":0.2068074768498308,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2008346671","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9891712,0.0010100486,0.0049257395,0.00013374143,0.000028640346,0.0000074960026,0.00069056486,0.00012083522,0.003911693],"genre_scores_gemma":[0.9949195,0.00034116357,0.0017679603,0.00004845313,0.000009851636,0.000017038554,0.00063566375,0.000050107425,0.0022103311],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9997898,0.00003349169,0.000015274038,0.000055319986,0.000058038462,0.000048082275],"domain_scores_gemma":[0.9997029,0.00012316104,0.000062358704,0.000036711408,0.000024691853,0.00005021234],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00014045587,0.00028086573,0.00024709548,0.00077204074,0.00018857437,0.00033394,0.0002804887,0.00035052397,0.0031410109],"category_scores_gemma":[0.00035175137,0.0003359602,0.00023987709,0.00026439285,0.0003301263,0.0001601225,0.00035334256,0.0003829176,0.00073193916],"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":[0.00030022804,0.0000065970753,0.0037976478,0.000029723202,0.000027236916,0.00040588094,0.000078135425,0.000056994326,0.99239916,0.00053396553,0.00006711206,0.0022972757],"study_design_scores_gemma":[0.00003978196,0.00014504198,0.1145959,0.000011526435,0.00010955769,0.005151159,0.00018031891,0.0005101131,0.8754467,0.0008454541,0.0029531743,0.000011350873],"about_ca_topic_score_codex":0.000789096,"about_ca_topic_score_gemma":0.0014857139,"teacher_disagreement_score":0.0031410109,"about_ca_system_score_codex":0.0001955708,"about_ca_system_score_gemma":0.0001247284,"threshold_uncertainty_score":0.010507762},"labels":[],"label_agreement":null},{"id":"W2009408130","doi":"10.1210/jc.2014-3098","title":"Novel Microdeletions Affecting the GNAS Locus in Pseudohypoparathyroidism: Characterization of the Underlying Mechanisms","year":2015,"lang":"en","type":"article","venue":"The Journal of Clinical Endocrinology & Metabolism","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":58,"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 de Sherbrooke","funders":"Instituto de Salud Carlos III; Agence Nationale de la Recherche; Marmara Üniversitesi; Ministero della Salute; Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico; Institut National de la Santé et de la Recherche Médicale; Università degli Studi di Torino; Università degli Studi di Milano; Université Paris-Sud; Aix-Marseille Université","keywords":"GNAS complex locus; Pseudohypoparathyroidism; Genetics; Locus (genetics); Biology; Haploinsufficiency; Multiplex ligation-dependent probe amplification; Phenotype; Gene; Exon; Medicine; Internal medicine; Parathyroid hormone","score_opus":0.07914498551181033,"score_gpt":0.34857838084654236,"score_spread":0.26943339533473204,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2009408130","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9982515,0.00031657537,0.0011177683,0.000024141054,0.0000026845505,0.00001121591,0.00009870881,0.000020927038,0.00015646065],"genre_scores_gemma":[0.99860734,0.000118217045,0.0009918498,0.000014480145,0.00000519147,0.000012726097,0.0001643648,0.0000038125715,0.000081956554],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9998615,0.000014615165,0.000015432835,0.00004524263,0.000041286545,0.000021985288],"domain_scores_gemma":[0.99968076,0.00013764038,0.00008357153,0.000027176296,0.000025849977,0.000045026143],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00012181827,0.00030684366,0.00024463085,0.000812528,0.00014497514,0.00017464506,0.0002783548,0.00039492617,0.0010345037],"category_scores_gemma":[0.0007037119,0.000118332704,0.00018812952,0.00037905233,0.00046445118,0.00015286801,0.00032909622,0.0003165365,0.00018261823],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00084738893,0.00011691641,0.32440516,0.00026263128,0.00011081443,0.042928737,0.00084880425,0.0014168996,0.5994136,0.00040492625,0.00020161839,0.029042529],"study_design_scores_gemma":[0.000098261546,0.00055929064,0.6976525,0.00002674751,0.00018692255,0.18915042,0.00027814257,0.0030821348,0.10578367,0.0004266675,0.0027282252,0.00002706791],"about_ca_topic_score_codex":0.00043620734,"about_ca_topic_score_gemma":0.0004377905,"teacher_disagreement_score":0.0010345037,"about_ca_system_score_codex":0.00018186285,"about_ca_system_score_gemma":0.000116513,"threshold_uncertainty_score":0.003460765},"labels":[],"label_agreement":null},{"id":"W2010123584","doi":"10.1016/j.diff.2011.01.007","title":"Developmental regulation of somatic imprints","year":2011,"lang":"en","type":"review","venue":"Differentiation","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":71,"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; Genomic imprinting; Epigenetics; DNA methylation; Genetics; Differentially methylated regions; Germline; Somatic cell; Allele; Methylation; Imprinting (psychology); Gene; Gene expression","score_opus":0.033754861202277074,"score_gpt":0.2729172209514721,"score_spread":0.239162359749195,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2010123584","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":[0.00016095293,0.9979673,0.00034526322,0.00019495338,0.0002463448,0.0000024778935,0.000018096121,0.00001099144,0.0010535956],"genre_scores_gemma":[0.001045393,0.997544,0.0002720178,0.00012433804,0.00024768946,0.0000041224234,0.000032521562,0.0000019757242,0.0007278578],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.9998306,0.000025048377,0.000021917534,0.000035001685,0.000064722124,0.00002269511],"domain_scores_gemma":[0.9998301,0.000073413576,0.000031629545,0.000008608193,0.000035271816,0.000021006217],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00047812174,0.0011372274,0.0012780105,0.0015943531,0.0002358775,0.0011868384,0.0012385141,0.0009970773,0.0018837291],"category_scores_gemma":[0.0004557282,0.0003761126,0.00028131998,0.0021887722,0.0010642462,0.0011068422,0.0008135658,0.0015945884,0.0013382802],"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":[0.00012856098,0.00005189679,0.00027031024,0.008378406,0.00007899555,0.00051339716,0.000057443416,0.0009589894,0.009566055,0.009733035,0.0311101,0.9391527],"study_design_scores_gemma":[0.000019141722,0.000032482203,0.0009424138,0.000957882,0.00006904719,0.0014774097,0.000054014497,0.00015680928,0.0024979494,0.00420362,0.98956794,0.000021235493],"about_ca_topic_score_codex":0.0009330586,"about_ca_topic_score_gemma":0.0015950522,"teacher_disagreement_score":0.0018837291,"about_ca_system_score_codex":0.0009227067,"about_ca_system_score_gemma":0.0008824298,"threshold_uncertainty_score":0.006694734},"labels":[],"label_agreement":null},{"id":"W2011000812","doi":"10.2217/epi.10.61","title":"Genetic and Epigenetic Dysregulation of Imprinted Genes In The Brain","year":2010,"lang":"en","type":"review","venue":"Epigenomics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":20,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Children’s Health Research Institute; Lawson Health Research Institute; Western University","funders":"Canadian Institutes of Health Research; International Rett Syndrome Foundation","keywords":"Genomic imprinting; Epigenetics; Biology; Imprinting (psychology); Gene; Genetics; Function (biology); Allele; Regulation of gene expression; Loss function; Phenotype; Epigenesis; DNA methylation; Gene expression; Neuroscience","score_opus":0.018345341647778287,"score_gpt":0.2819315596565236,"score_spread":0.2635862180087453,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2011000812","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":[0.0008573531,0.9956727,0.00074638205,0.0003269152,0.000142574,0.0000033956185,0.000027345635,0.000027039268,0.0021962381],"genre_scores_gemma":[0.0033842956,0.99488395,0.0004044602,0.0001210475,0.000105361534,0.0000050437848,0.00002836879,0.0000026163518,0.0010647918],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.99992096,0.000013636278,0.000009751079,0.000016662676,0.00003187811,0.0000071716822],"domain_scores_gemma":[0.99992824,0.000027120828,0.000015554868,0.0000040081045,0.000015876873,0.000009253146],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00021306096,0.00055468315,0.00063738954,0.0009784838,0.00013422406,0.00046228818,0.00052340486,0.0007040244,0.0014629798],"category_scores_gemma":[0.00022286086,0.00013851549,0.00015554644,0.0009820837,0.0004927442,0.0005976571,0.0004051848,0.00061059726,0.0014272967],"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":[0.00007708258,0.000035628294,0.00055861386,0.004742812,0.00007503066,0.001162474,0.000066365676,0.0005630244,0.026797332,0.00854551,0.014564881,0.9428113],"study_design_scores_gemma":[0.00001683293,0.00008376325,0.004132847,0.0012418461,0.00008682846,0.009562455,0.00010604158,0.00021544054,0.015037292,0.006227977,0.96326095,0.000027826645],"about_ca_topic_score_codex":0.0006084681,"about_ca_topic_score_gemma":0.00093727896,"teacher_disagreement_score":0.0014629798,"about_ca_system_score_codex":0.0005016142,"about_ca_system_score_gemma":0.00037184617,"threshold_uncertainty_score":0.0048941374},"labels":[],"label_agreement":null},{"id":"W2011113753","doi":"10.1007/s00018-014-1714-0","title":"What does genetics tell us about imprinting and the placenta connection?","year":2014,"lang":"en","type":"review","venue":"Cellular and Molecular Life Sciences","topic":"Genetic Syndromes and Imprinting","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":"University of Toronto","funders":"","keywords":"Genomic imprinting; Imprinting (psychology); Placentation; Biology; Epigenetics; Genetics; Placenta; Gene; Evolutionary biology; DNA methylation; Fetus; Gene expression; Pregnancy","score_opus":0.014176130280955672,"score_gpt":0.27660229299133227,"score_spread":0.2624261627103766,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2011113753","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":[0.000062426625,0.9980744,0.00009357923,0.0010655647,0.00026396455,7.962275e-7,0.000008725309,0.0000029503087,0.00042750005],"genre_scores_gemma":[0.0006396505,0.9980692,0.00010164127,0.0004830585,0.0004607212,0.000002175495,0.0000108993445,9.977501e-7,0.00023168605],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.99978095,0.00006092066,0.000025639594,0.000037743404,0.000068741785,0.00002599026],"domain_scores_gemma":[0.99928623,0.00050783413,0.000052580337,0.000020954923,0.00008489473,0.000047556274],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0009987097,0.0007252966,0.0016757589,0.0015877049,0.00038189488,0.0014677822,0.0011492344,0.0023767236,0.002691599],"category_scores_gemma":[0.0018743292,0.00030764067,0.00043092252,0.0021471821,0.0017482993,0.0023878282,0.0008879268,0.002813164,0.00100323],"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":[0.00017117437,0.00005297079,0.0007188939,0.012441053,0.00020074283,0.0009968572,0.00018148856,0.0005990697,0.0016323522,0.026920864,0.06427771,0.89180684],"study_design_scores_gemma":[0.000024043466,0.000039841507,0.0010622957,0.0031671843,0.00014199878,0.0026909104,0.00018680366,0.0000917051,0.000305224,0.015272767,0.9769866,0.00003064684],"about_ca_topic_score_codex":0.0019351222,"about_ca_topic_score_gemma":0.0025221738,"teacher_disagreement_score":0.002691599,"about_ca_system_score_codex":0.00089856965,"about_ca_system_score_gemma":0.0016816229,"threshold_uncertainty_score":0.009004295},"labels":[],"label_agreement":null},{"id":"W2011643481","doi":"10.1177/08830738060210042201","title":"Diagnosing Sotos Syndrome in the Setting of Global Developmental Delay and Macrocephaly","year":2006,"lang":"en","type":"article","venue":"Journal of Child Neurology","topic":"Genetic Syndromes and Imprinting","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":"McGill University; McGill University Health Centre; Montreal Children's Hospital","funders":"","keywords":"Sotos syndrome; Macrocephaly; Bone age; Pediatrics; Medicine; Gigantism; Internal medicine","score_opus":0.0034159345315114206,"score_gpt":0.20904925262427945,"score_spread":0.20563331809276802,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2011643481","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9991086,0.00014176934,0.00015082247,0.000045959925,0.0000065435547,0.000010611458,0.000024263381,0.000008249486,0.00050307706],"genre_scores_gemma":[0.99918324,0.00021560011,0.00040257708,0.000043074728,0.000024619358,0.000008026958,0.000051112325,0.0000032290984,0.00006847632],"study_design_codex":"observational","study_design_gemma":"case_report","domain_scores_codex":[0.9993036,0.00017581794,0.00009332101,0.00012554972,0.00013538043,0.00016638206],"domain_scores_gemma":[0.9981312,0.0006553736,0.0005258946,0.000063169035,0.0001468982,0.00047741347],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0006587414,0.00066337705,0.0005374925,0.0016739459,0.0005884346,0.0005984337,0.000506739,0.0008691707,0.0014455492],"category_scores_gemma":[0.0049100956,0.0003980087,0.00017385567,0.00060474884,0.0008056033,0.00085249275,0.00073122355,0.0005968309,0.00028309712],"study_design_candidate":"case_report","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00009879579,0.00002457829,0.96745324,0.0000142958,0.0000063751563,0.028229097,0.00021322233,0.000067292734,0.0016900412,0.000044960892,0.00012989854,0.0020281724],"study_design_scores_gemma":[0.000033287946,0.00070548285,0.7086263,0.000044193588,0.000050245475,0.2840768,0.0020742712,0.0010913153,0.0021903324,0.0002624853,0.000822654,0.000022704045],"about_ca_topic_score_codex":0.0012886617,"about_ca_topic_score_gemma":0.0017680126,"teacher_disagreement_score":0.0016739459,"about_ca_system_score_codex":0.00024466866,"about_ca_system_score_gemma":0.00049577124,"threshold_uncertainty_score":0.0048359036},"labels":[],"label_agreement":null},{"id":"W2011958888","doi":"10.1007/s00335-004-2434-9","title":"Increased plasticity of genomic imprinting of Dlk1 in brain is due to genetic and epigenetic factors","year":2005,"lang":"en","type":"article","venue":"Mammalian Genome","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":21,"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; Royal Victoria Hospital; McGill University Health Centre; Royal Victoria Regional Health Centre","funders":"Canadian Institutes of Health Research; Genome Canada; Burroughs Wellcome Fund","keywords":"Genomic imprinting; Biology; Epigenetics; Imprinting (psychology); Human genetics; Genetics; Epigenesis; DNA methylation; Computational biology; Gene; Gene expression","score_opus":0.008027411001838255,"score_gpt":0.21961980099758147,"score_spread":0.2115923899957432,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2011958888","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9888952,0.0031265158,0.003933804,0.00033427685,0.000055802593,0.000009925775,0.0006632663,0.00024104156,0.0027403003],"genre_scores_gemma":[0.9973667,0.0005751664,0.00061618234,0.0000371468,0.00001025102,0.000009003374,0.00023189599,0.00003294246,0.001120699],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9998894,0.000013150635,0.000010901251,0.000037000173,0.000023466135,0.000026136953],"domain_scores_gemma":[0.9998443,0.000032845914,0.000049077214,0.000024452,0.000009816125,0.00003947344],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00008969901,0.00029851205,0.00022428717,0.0006012809,0.00017022165,0.0002780572,0.00030825872,0.00016123141,0.0024203185],"category_scores_gemma":[0.00028750818,0.00017225511,0.00016891558,0.00024119324,0.00044248247,0.00022856334,0.0004257953,0.00041211792,0.00021215242],"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":[0.0002613772,0.000009839392,0.0017780286,0.00003891975,0.000019432566,0.00048162,0.000023399922,0.00010662714,0.99370956,0.00053405267,0.00008159583,0.0029555405],"study_design_scores_gemma":[0.000023160479,0.000070168484,0.048665386,0.0000065016498,0.000056935914,0.002119299,0.00006637883,0.0003997281,0.94588226,0.00047332462,0.0022271147,0.000009755144],"about_ca_topic_score_codex":0.00084145245,"about_ca_topic_score_gemma":0.0011556431,"teacher_disagreement_score":0.0024203185,"about_ca_system_score_codex":0.000361157,"about_ca_system_score_gemma":0.00020329919,"threshold_uncertainty_score":0.008096755},"labels":[],"label_agreement":null},{"id":"W2012362930","doi":"10.1007/s00335-013-9454-2","title":"Recommendations for the investigation of animal models of Prader–Willi syndrome","year":2013,"lang":"en","type":"article","venue":"Mammalian Genome","topic":"Genetic Syndromes and Imprinting","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 Alberta","funders":"Foundation for Prader-Willi Research","keywords":"Human genetics; Biology; Computational biology; Genetics; Evolutionary biology; Bioinformatics; Gene","score_opus":0.03346389664720976,"score_gpt":0.2451336213330381,"score_spread":0.21166972468582834,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2012362930","genre_codex":"commentary","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":[0.011422337,0.0711954,0.11098428,0.576743,0.051955942,0.009995758,0.010637403,0.00791164,0.14915422],"genre_scores_gemma":[0.01821962,0.07106139,0.51165766,0.22926138,0.012121331,0.016840069,0.009997119,0.0016507203,0.12919076],"study_design_codex":"not_applicable","study_design_gemma":"theoretical_or_conceptual","domain_scores_codex":[0.98230827,0.0088337315,0.0034915286,0.00094170676,0.0033281846,0.0010965072],"domain_scores_gemma":[0.88484377,0.030898137,0.009178136,0.011161533,0.054255378,0.009663035],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.036373958,0.002395583,0.003674324,0.007684138,0.0025815866,0.0032110708,0.010011652,0.023536142,0.031698544],"category_scores_gemma":[0.04135196,0.0021206632,0.0049054497,0.0041465447,0.003983439,0.004738968,0.0028861812,0.0146150375,0.023293605],"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":[0.0016381758,0.0015885864,0.003864466,0.004781207,0.00036563104,0.002295298,0.0005771289,0.0014332082,0.023787074,0.010908083,0.79507315,0.15368794],"study_design_scores_gemma":[0.0011624972,0.0012001013,0.011559492,0.010755196,0.0011509572,0.003370846,0.0012555076,0.0012005717,0.008659716,0.016753623,0.9425667,0.00036476483],"about_ca_topic_score_codex":0.014185177,"about_ca_topic_score_gemma":0.027252372,"teacher_disagreement_score":0.036373958,"about_ca_system_score_codex":0.0021728799,"about_ca_system_score_gemma":0.009676306,"threshold_uncertainty_score":0.19236618},"labels":[],"label_agreement":null},{"id":"W2012768593","doi":"10.1159/000354038","title":"Interstitial Deletions at 6q14.1q15 Associated with Developmental Delay and a Marfanoid Phenotype","year":2013,"lang":"en","type":"article","venue":"Molecular Syndromology","topic":"Genetic Syndromes and Imprinting","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 Calgary; Alberta Health; Alberta Health Services; Alberta Children's Hospital","funders":"","keywords":"Haploinsufficiency; Phenotype; Arachnodactyly; Scoliosis; Marfan syndrome; Genetics; Pectus excavatum; Comparative genomic hybridization; Microdeletion syndrome; Cataracts; Short stature; Biology; Chromosome; Developmental disorder; Medicine; Gene; Autism; Pediatrics; Internal medicine","score_opus":0.005318222675318374,"score_gpt":0.1928868455536051,"score_spread":0.18756862287828674,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2012768593","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99721634,0.00036944306,0.0011835016,0.000093076276,0.000011693473,0.000011354334,0.000066934095,0.000033691576,0.0010138768],"genre_scores_gemma":[0.9978709,0.00024258517,0.0011792283,0.000042785887,0.000025104284,0.0000070304077,0.0000795754,0.000007531084,0.00054526987],"study_design_codex":"case_report","study_design_gemma":"observational","domain_scores_codex":[0.99975604,0.00003729542,0.00002627529,0.00008229439,0.00005332799,0.000044880682],"domain_scores_gemma":[0.9994399,0.00018405348,0.00019501068,0.00002592437,0.000024954654,0.00013020304],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0002300279,0.00094241166,0.00044229478,0.0010277198,0.00036396045,0.00025996278,0.00034664432,0.00066727883,0.0015942849],"category_scores_gemma":[0.00095587404,0.00027587265,0.0002845844,0.0004890537,0.00070682314,0.00021212267,0.0005602401,0.0004822474,0.00025805022],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0007109468,0.00018567393,0.114504725,0.00019203336,0.00014007973,0.6198947,0.0016867805,0.0008301148,0.23744464,0.0019974723,0.0005853926,0.02182747],"study_design_scores_gemma":[0.00010315574,0.00058119115,0.1461699,0.000043076947,0.00012663724,0.82815367,0.00027496,0.0007231509,0.020814527,0.00067688135,0.0023020692,0.000030782125],"about_ca_topic_score_codex":0.0006197979,"about_ca_topic_score_gemma":0.0009041267,"teacher_disagreement_score":0.0015942849,"about_ca_system_score_codex":0.00019045126,"about_ca_system_score_gemma":0.00021765397,"threshold_uncertainty_score":0.005333364},"labels":[],"label_agreement":null},{"id":"W2013013633","doi":"10.1007/s10048-007-0086-0","title":"Evaluation of autism traits in Angelman syndrome: a resource to unfold autism genes","year":2007,"lang":"en","type":"article","venue":"Neurogenetics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":99,"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","funders":"","keywords":"Autism; Angelman syndrome; UBE3A; Autism Diagnostic Observation Schedule; Neurodevelopmental disorder; Intellectual disability; Autism spectrum disorder; Psychology; Genetics; Uniparental disomy; Heritability of autism; Psychiatry; Clinical psychology; Biology; Gene; Chromosome; Ubiquitin ligase","score_opus":0.023731863856325527,"score_gpt":0.2810377759084099,"score_spread":0.25730591205208436,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2013013633","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.74600697,0.01470078,0.10861934,0.0024616008,0.00023664044,0.0010342014,0.061338946,0.008085839,0.05751578],"genre_scores_gemma":[0.7686356,0.009135191,0.15693712,0.000672058,0.00022692094,0.0010448183,0.038097393,0.0018268815,0.023424055],"study_design_codex":"design_other","study_design_gemma":"observational","domain_scores_codex":[0.9995448,0.00012776448,0.00007216484,0.000049256465,0.00015286855,0.000053041338],"domain_scores_gemma":[0.99757296,0.0009819341,0.00020005308,0.00027668683,0.00059394044,0.00037448885],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0012791753,0.0006939896,0.0007363577,0.0048198537,0.00046954956,0.00059742475,0.0006208177,0.00032171523,0.0059783035],"category_scores_gemma":[0.0035387522,0.00022797633,0.00039204216,0.0014112714,0.00016339583,0.00042331984,0.0009413482,0.0003466417,0.0018331837],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0019391348,0.00039850833,0.1797982,0.00079687795,0.00024379512,0.014010241,0.0013475606,0.0025965222,0.10833167,0.0018130227,0.055945124,0.6327794],"study_design_scores_gemma":[0.00044956413,0.0008809034,0.5403341,0.00063307805,0.0008104755,0.059718404,0.0021562693,0.009179412,0.16244829,0.007925288,0.21519266,0.0002715613],"about_ca_topic_score_codex":0.0034170405,"about_ca_topic_score_gemma":0.006029737,"teacher_disagreement_score":0.0059783035,"about_ca_system_score_codex":0.0003660556,"about_ca_system_score_gemma":0.00081984967,"threshold_uncertainty_score":0.019999444},"labels":[],"label_agreement":null},{"id":"W2013044331","doi":"10.1080/01677060600685840","title":"THE INHERITANCE OF COGNITIVE SKILLS: DOES GENOMIC IMPRINTING PLAY A ROLE?","year":2006,"lang":"en","type":"article","venue":"Journal of Neurogenetics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","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":"York University; SickKids Foundation; Hospital for Sick Children","funders":"","keywords":"Imprinting (psychology); Genomic imprinting; Biology; Cognition; Neuroscience; Psychology; Population; Genetics; Developmental psychology; Evolutionary biology; Gene; DNA methylation; Gene expression; Medicine","score_opus":0.004083189693964786,"score_gpt":0.22040159442597507,"score_spread":0.21631840473201028,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2013044331","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99412787,0.002483347,0.0010047858,0.0005417129,0.000012567652,0.0000042664005,0.00015603205,0.000017059176,0.001652387],"genre_scores_gemma":[0.99862754,0.0007498006,0.00025489536,0.000049738625,0.000022763337,0.0000037864,0.00003981713,0.0000041461835,0.00024744566],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9996902,0.00008469803,0.00001703082,0.00009065402,0.00006956633,0.000047838377],"domain_scores_gemma":[0.9984835,0.0006609085,0.00038738077,0.00016718419,0.000121852114,0.00017910331],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0005573852,0.0006293713,0.00052522303,0.0012467727,0.0002474175,0.0005233121,0.0004542016,0.0005017024,0.0027928278],"category_scores_gemma":[0.0035633116,0.00014973471,0.00014105569,0.0008894764,0.0015025288,0.0005693389,0.0004947772,0.00042335739,0.0002730242],"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":[0.00043689494,0.00010688829,0.9104862,0.000115905816,0.000236869,0.0020155662,0.0012307643,0.00028619525,0.02496701,0.0030386387,0.00023975145,0.056839336],"study_design_scores_gemma":[0.000007444133,0.00017738961,0.9938385,0.000017719982,0.00006180452,0.0018127124,0.00032361862,0.000343662,0.001623658,0.0014523407,0.00033212657,0.00000903588],"about_ca_topic_score_codex":0.0018398041,"about_ca_topic_score_gemma":0.0014964439,"teacher_disagreement_score":0.0027928278,"about_ca_system_score_codex":0.00023556172,"about_ca_system_score_gemma":0.00033729026,"threshold_uncertainty_score":0.009342968},"labels":[],"label_agreement":null},{"id":"W2013787654","doi":"10.1534/genetics.103.026211","title":"Intralocus Sexual Conflict Can Drive the Evolution of Genomic Imprinting","year":2004,"lang":"en","type":"article","venue":"Genetics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":225,"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; Queen's University","funders":"","keywords":"Imprinting (psychology); Genomic imprinting; Biology; Epigenetics; Evolutionary biology; Sexual dimorphism; Genetics; Allele; DNA methylation; Gene; Zoology; Gene expression","score_opus":0.00867627261508725,"score_gpt":0.2246560516171975,"score_spread":0.21597977900211027,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2013787654","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9863116,0.0019472922,0.0040026936,0.0004895191,0.000032057844,0.0000065924346,0.00008563373,0.000038544953,0.007086062],"genre_scores_gemma":[0.9972904,0.00066244334,0.00088660105,0.0001446005,0.00001924296,0.000006554372,0.00006970073,0.000016895397,0.0009035386],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.99963355,0.00010399242,0.000020904394,0.00009110632,0.000080356345,0.000070206464],"domain_scores_gemma":[0.99887794,0.0004800932,0.00028358662,0.00014307909,0.000047014888,0.00016817084],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00058165187,0.0002139059,0.0003158007,0.00044223174,0.0004425451,0.00078330364,0.0004703348,0.0005786281,0.0025163672],"category_scores_gemma":[0.0016191378,0.00017640724,0.00020136288,0.00041021942,0.00092918176,0.00072626054,0.0012456576,0.0006747301,0.00044948465],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0008284357,0.00012891808,0.096500784,0.00030859082,0.00021953139,0.004831151,0.001589804,0.0041463287,0.7778691,0.0342916,0.00088199467,0.0784038],"study_design_scores_gemma":[0.00016490881,0.00088987127,0.5805541,0.00012706818,0.00034660232,0.018526813,0.0026865636,0.019091083,0.21949932,0.115940474,0.041921392,0.00025179714],"about_ca_topic_score_codex":0.0001817254,"about_ca_topic_score_gemma":0.00037103368,"teacher_disagreement_score":0.0025163672,"about_ca_system_score_codex":0.00027950283,"about_ca_system_score_gemma":0.00018467377,"threshold_uncertainty_score":0.008418083},"labels":[],"label_agreement":null},{"id":"W2014049913","doi":"10.1210/en.2010-0709","title":"Impaired Hypothalamic Regulation of Endocrine Function and Delayed Counterregulatory Response to Hypoglycemia in Magel2-Null Mice","year":2011,"lang":"en","type":"article","venue":"Endocrinology","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":79,"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 Institute of Diabetes and Digestive and Kidney Diseases; Canadian Institutes of Health Research","keywords":"Endocrinology; Internal medicine; Ghrelin; Corticosterone; Hypoglycemia; Endocrine system; Medicine; Basal (medicine); Hypothalamus; Circadian rhythm; Null allele; Insulin; Hormone; Biology; Phenotype; Gene","score_opus":0.013549559793782178,"score_gpt":0.22500294999875048,"score_spread":0.2114533902049683,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2014049913","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99288106,0.00044253646,0.004260482,0.00013031498,0.00006095409,0.000022987859,0.0012290148,0.00023906224,0.0007336529],"genre_scores_gemma":[0.9868601,0.00058726943,0.0053912946,0.00014907791,0.000036197718,0.00012255555,0.0015593737,0.00025391215,0.00504014],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9997291,0.000025992731,0.000045772755,0.00008305403,0.00007498771,0.0000411321],"domain_scores_gemma":[0.99948955,0.000057541736,0.0002089348,0.000049377573,0.000024603009,0.00016992792],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00022785833,0.0009332791,0.00038850046,0.000981921,0.00021691085,0.00047364095,0.0005665397,0.0006445085,0.0023239385],"category_scores_gemma":[0.0002888583,0.00046249997,0.00049682835,0.00024316632,0.00061377685,0.00036227668,0.00050501205,0.0010038471,0.0004846913],"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":[0.00029115894,0.000028023976,0.000543844,0.000028467679,0.000012517868,0.00030125884,0.00002959374,0.00009032328,0.99770665,0.00013716632,0.000044521577,0.0007864055],"study_design_scores_gemma":[0.00020263968,0.00057765556,0.03222044,0.000027077409,0.00007591781,0.0033066599,0.0001557499,0.0023272028,0.95700693,0.00031940438,0.003740792,0.000039559633],"about_ca_topic_score_codex":0.00047985493,"about_ca_topic_score_gemma":0.0009312335,"teacher_disagreement_score":0.0023239385,"about_ca_system_score_codex":0.00034479893,"about_ca_system_score_gemma":0.00023410568,"threshold_uncertainty_score":0.0077742934},"labels":[],"label_agreement":null},{"id":"W2016293553","doi":"10.1006/geno.2001.6549","title":"Imprinting Status of 11p15 Genes in Beckwith–Wiedemann Syndrome Patients with CDKN1C Mutations","year":2001,"lang":"en","type":"article","venue":"Genomics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":60,"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; University of Toronto; Hospital for Sick Children","funders":"National Cancer Institute","keywords":"Beckwith–Wiedemann syndrome; Imprinting (psychology); Genomic imprinting; Biology; Genetics; Pedigree chart; Proband; Gene; Phenotype; Germline mutation; Mutation; Gene expression; DNA methylation","score_opus":0.006807924696443324,"score_gpt":0.21335701509634938,"score_spread":0.20654909039990607,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2016293553","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9984889,0.00019792677,0.000122022335,0.00005801742,0.000007815384,0.0000036898186,0.00012510722,0.000007932299,0.0009884931],"genre_scores_gemma":[0.9994709,0.00009148953,0.00018119076,0.000017574686,0.0000062277404,0.0000033303108,0.000058597932,0.0000042235715,0.00016638944],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9997776,0.000032603057,0.000033185555,0.00005339438,0.00004329084,0.00005999789],"domain_scores_gemma":[0.99964464,0.00015914711,0.00007513757,0.000014419013,0.00002318048,0.00008330927],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0001483198,0.0007480312,0.00030800956,0.0017559263,0.00043331788,0.0004608457,0.00034170118,0.0004930588,0.0024935922],"category_scores_gemma":[0.0011391959,0.00028632837,0.00019289656,0.00081071444,0.0004448932,0.00025608944,0.00030395738,0.00023653511,0.00021152283],"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":[0.003011885,0.00017527748,0.67910475,0.00008136256,0.00015512382,0.180598,0.0014006699,0.0012325456,0.10807485,0.0009432521,0.00090054685,0.02432165],"study_design_scores_gemma":[0.00011151714,0.00026774668,0.760291,0.000037398655,0.00032605737,0.20639327,0.00081885565,0.0020268306,0.026981398,0.0007600172,0.0019353214,0.000050673825],"about_ca_topic_score_codex":0.0036150669,"about_ca_topic_score_gemma":0.0026737433,"teacher_disagreement_score":0.0036150669,"about_ca_system_score_codex":0.00036130557,"about_ca_system_score_gemma":0.00030376413,"threshold_uncertainty_score":0.008341908},"labels":[],"label_agreement":null},{"id":"W2016355843","doi":"10.1016/j.metabol.2008.07.012","title":"Impact of genetic and epigenetic factors from early life to later disease","year":2008,"lang":"en","type":"review","venue":"Metabolism","topic":"Genetic Syndromes and Imprinting","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":"Centre Hospitalier de l’Université de Montréal","funders":"","keywords":"Epigenetics; Epigenomics; Adaptation (eye); Biology; Disease; Genomic imprinting; Genetics; Genome; Epigenesis; DNA methylation; Evolutionary biology; Gene; Medicine; Neuroscience; Internal medicine; Gene expression","score_opus":0.02338435163053608,"score_gpt":0.29266239695386287,"score_spread":0.2692780453233268,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2016355843","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":[0.00019033435,0.9984366,0.0002145236,0.00036094303,0.00021795361,0.0000014626517,0.00001795511,0.0000069700063,0.0005533],"genre_scores_gemma":[0.0010236276,0.9977379,0.0002550236,0.00019895704,0.00024628956,0.000003396236,0.000026074247,0.0000014138781,0.0005072171],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.99983287,0.000029755683,0.000024356996,0.00004489697,0.000052812742,0.000015380028],"domain_scores_gemma":[0.99966645,0.0001901429,0.000038589853,0.000013101043,0.00006675,0.000024986246],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00062482484,0.0010701407,0.0018470163,0.0010848462,0.00021876894,0.0011098117,0.001020096,0.0013543972,0.0019915674],"category_scores_gemma":[0.0006900744,0.00027964945,0.00038421148,0.001539858,0.00076544733,0.0009854443,0.0005963865,0.0016448974,0.0010348872],"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":[0.00025018523,0.000052896998,0.0007932027,0.0066483407,0.00018855729,0.000797365,0.00006070283,0.0007078536,0.0057641244,0.0042873896,0.026610121,0.95383936],"study_design_scores_gemma":[0.00004752505,0.00010936657,0.004091067,0.0020054367,0.00033126283,0.0039297547,0.00014515936,0.00018109618,0.0025700582,0.0055974727,0.9809497,0.00004215086],"about_ca_topic_score_codex":0.0011822557,"about_ca_topic_score_gemma":0.0024975925,"teacher_disagreement_score":0.0019915674,"about_ca_system_score_codex":0.0007327872,"about_ca_system_score_gemma":0.00075343647,"threshold_uncertainty_score":0.006662488},"labels":[],"label_agreement":null},{"id":"W2016686236","doi":"10.1002/jbmr.461","title":"Parathyroid hormone signaling via Gαs is selectively inhibited by an NH2-terminally truncated Gαs: Implications for pseudohypoparathyroidism","year":2011,"lang":"en","type":"article","venue":"Journal of Bone and Mineral Research","topic":"Genetic Syndromes and Imprinting","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":"Royal Victoria Regional Health Centre; Royal Victoria Hospital; Victoria Hospital; McGill University","funders":"National Institute of Diabetes and Digestive and Kidney Diseases; Canadian Institutes of Health Research","keywords":"Pseudohypoparathyroidism; Internal medicine; Endocrinology; Parathyroid hormone; Parathyroid hormone receptor; Gs alpha subunit; GNAS complex locus; Receptor; Chemistry; Calcitonin; G protein; Biology; Hormone receptor; Medicine; Calcium; Biochemistry","score_opus":0.06707259939033473,"score_gpt":0.34368085917957547,"score_spread":0.27660825978924075,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2016686236","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9962788,0.0014934307,0.0010934386,0.0002485679,0.00003054154,0.0000138182,0.0001106315,0.000039568047,0.0006912208],"genre_scores_gemma":[0.9969747,0.00113427,0.0009909213,0.00014538218,0.000014002876,0.00001277418,0.00018844953,0.000010102066,0.00052930886],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99991584,0.000019262367,0.000008649807,0.000016105394,0.000020339216,0.00001971209],"domain_scores_gemma":[0.99993014,0.000015060475,0.000023099083,0.000009793246,0.0000051830857,0.00001669867],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00014447696,0.00030528285,0.00021245462,0.000097172655,0.00008846406,0.00027078672,0.00025420752,0.00030888885,0.00072003884],"category_scores_gemma":[0.0001525049,0.000099928126,0.00032758273,0.00010122516,0.00043702894,0.00014951685,0.00015533152,0.0005014101,0.00022429253],"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":[0.00022637696,0.000010653049,0.00035296698,0.000019740683,0.000007187085,0.0001915059,0.000008210272,0.000075772354,0.9982494,0.00015992708,0.000026555459,0.0006718413],"study_design_scores_gemma":[0.000253206,0.0018948483,0.023100484,0.000017385237,0.000091181035,0.0060589854,0.00010614634,0.002391534,0.9563478,0.00033800365,0.009385025,0.000015358037],"about_ca_topic_score_codex":0.00042166092,"about_ca_topic_score_gemma":0.00043868998,"teacher_disagreement_score":0.00072003884,"about_ca_system_score_codex":0.00026073898,"about_ca_system_score_gemma":0.00013490462,"threshold_uncertainty_score":0.002408743},"labels":[],"label_agreement":null},{"id":"W2016725540","doi":"10.1002/acn3.126","title":"Unusual Stüve‐Wiedemann syndrome with complete maternal chromosome 5 isodisomy","year":2014,"lang":"en","type":"article","venue":"Annals of Clinical and Translational Neurology","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","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":"London Health Sciences Centre; Western University","funders":"National Institutes of Health; National Heart, Lung, and Blood Institute; Helse Vest","keywords":"Medicine; Beckwith–Wiedemann syndrome; Chromosome; Genetics; Gene; Biology","score_opus":0.05766965772263427,"score_gpt":0.3323834499655032,"score_spread":0.2747137922428689,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2016725540","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99064225,0.00087461754,0.0019300452,0.00035698724,0.000069371585,0.00003860131,0.00030706532,0.0001766605,0.005604344],"genre_scores_gemma":[0.9961333,0.00056754623,0.0011786195,0.00012676307,0.0000627764,0.000024391744,0.00016572235,0.000029047407,0.001711793],"study_design_codex":"case_report","study_design_gemma":"case_report","domain_scores_codex":[0.99974436,0.000026884201,0.000025199697,0.00009268387,0.000052837484,0.00005810422],"domain_scores_gemma":[0.9996216,0.00011532771,0.0000948555,0.00003304365,0.000015959096,0.00011915793],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00012204663,0.0015001526,0.0005672427,0.001664306,0.0005793325,0.00041979592,0.00065048353,0.001225212,0.0035382712],"category_scores_gemma":[0.0012571436,0.0004932849,0.00035469327,0.000891176,0.0007089403,0.00042158135,0.00097528304,0.0005775,0.0005004926],"study_design_candidate":"case_report","study_design_consensus":"case_report","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00009963317,0.000021351854,0.006814925,0.000034916444,0.000024957275,0.9759017,0.00020266711,0.00012281262,0.011225083,0.00072513474,0.0003025,0.0045242803],"study_design_scores_gemma":[0.000015288015,0.00005498436,0.012447519,0.00000935398,0.000023973334,0.98399943,0.00004955689,0.00015180641,0.0021432764,0.00023368209,0.0008607196,0.000010392007],"about_ca_topic_score_codex":0.0010170246,"about_ca_topic_score_gemma":0.0013934645,"teacher_disagreement_score":0.0035382712,"about_ca_system_score_codex":0.00037708427,"about_ca_system_score_gemma":0.00033113526,"threshold_uncertainty_score":0.011836708},"labels":[],"label_agreement":null},{"id":"W2017331347","doi":"10.1016/s1567-133x(03)00113-3","title":"Prader–Willi syndrome transcripts are expressed in phenotypically significant regions of the developing mouse brain","year":2003,"lang":"en","type":"article","venue":"Gene Expression Patterns","topic":"Genetic Syndromes and Imprinting","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":"","keywords":"Biology; Forebrain; Phenotype; Gene; Genetics; Candidate gene; Genomic imprinting; Hindbrain; Gene expression; Endocrinology; Central nervous system; DNA methylation","score_opus":0.018783811972188397,"score_gpt":0.23437029238686372,"score_spread":0.21558648041467532,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2017331347","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99140716,0.0020077142,0.0040846467,0.00013112571,0.000021360469,0.000009026961,0.0004263299,0.00012118543,0.0017914119],"genre_scores_gemma":[0.9884035,0.0013924106,0.0041159955,0.00006213145,0.000020515994,0.000037132733,0.00077697175,0.00010356678,0.0050877454],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9997738,0.000023572493,0.0000138387595,0.00007266872,0.0000691742,0.000046973342],"domain_scores_gemma":[0.9996456,0.00006929744,0.00015562735,0.000028733612,0.00003347422,0.00006727308],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0001466483,0.0005490923,0.00030195317,0.0009546316,0.000250418,0.00047057224,0.0002703317,0.00034163342,0.0010337052],"category_scores_gemma":[0.00024692898,0.0005773231,0.00029291923,0.00024256772,0.00057609426,0.0003357433,0.00036385102,0.00079842407,0.00044497338],"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":[0.000046110104,0.0000024503645,0.00026796205,0.000010693356,0.0000046960236,0.00010800493,0.000021951722,0.00002548869,0.99899215,0.00011549144,0.000012943602,0.00039209478],"study_design_scores_gemma":[0.000031847412,0.00016292112,0.05234778,0.000018928551,0.00006688144,0.0028629496,0.00018037319,0.00047757776,0.94105834,0.00046122694,0.0023147333,0.000016476055],"about_ca_topic_score_codex":0.0006505046,"about_ca_topic_score_gemma":0.0011946731,"teacher_disagreement_score":0.0010337052,"about_ca_system_score_codex":0.00024459354,"about_ca_system_score_gemma":0.00019220807,"threshold_uncertainty_score":0.003458023},"labels":[],"label_agreement":null},{"id":"W2017472084","doi":"10.1002/gene.20027","title":"Loss‐of‐imprinting of <i>Peg1</i> in mouse interspecies hybrids is correlated with altered growth","year":2004,"lang":"en","type":"article","venue":"genesis","topic":"Genetic Syndromes and Imprinting","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 British Columbia","funders":"","keywords":"Biology; Hybrid; Allele; Genomic imprinting; Imprinting (psychology); Loss of heterozygosity; Genetics; Gene; Molecular biology; Gene expression; DNA methylation; Botany","score_opus":0.006878149184088171,"score_gpt":0.20624724860276855,"score_spread":0.1993690994186804,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2017472084","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99814284,0.00030563818,0.00070509425,0.000030702166,0.0000067428264,0.0000051932384,0.00020338663,0.00008206693,0.00051828113],"genre_scores_gemma":[0.9975503,0.00018360076,0.00045460177,0.000025700008,0.0000060728216,0.000015089449,0.00041907246,0.000044429522,0.0013010693],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99972194,0.000037234127,0.000034086883,0.00008776576,0.00006716616,0.0000517543],"domain_scores_gemma":[0.9995315,0.000066675275,0.00022536001,0.000042176514,0.000013230486,0.00012105984],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0001482518,0.00038595614,0.00018909635,0.0010776792,0.0001758277,0.00027284908,0.00022030073,0.0003395526,0.0017529991],"category_scores_gemma":[0.00016150468,0.00022302815,0.00022806764,0.00021789172,0.0003070892,0.00015008077,0.00040407316,0.0006832119,0.0003809181],"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":[0.00008614947,0.000015240591,0.0013220625,0.000008456432,0.000009438025,0.00012937859,0.000016000542,0.00002090256,0.9977526,0.000051927258,0.000013029952,0.0005748687],"study_design_scores_gemma":[0.000023781748,0.00048444833,0.1064654,0.000007141931,0.000059622358,0.003591026,0.0000986532,0.0005441254,0.88707876,0.000106510255,0.0015248038,0.000015679654],"about_ca_topic_score_codex":0.00036272802,"about_ca_topic_score_gemma":0.0007236342,"teacher_disagreement_score":0.0017529991,"about_ca_system_score_codex":0.00020392664,"about_ca_system_score_gemma":0.00008827413,"threshold_uncertainty_score":0.005864382},"labels":[],"label_agreement":null},{"id":"W2017994263","doi":"10.1067/mpd.2003.81","title":"Myeloid leukemia in Prader-Willi syndrome","year":2003,"lang":"en","type":"article","venue":"The Journal of Pediatrics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":53,"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":"Medicine; Myeloid leukemia; Leukemia; Epidemiology; Population; Cancer; Oncology; Internal medicine; Myeloid; Surveillance, Epidemiology, and End Results; Cancer registry; Environmental health","score_opus":0.008989734299718565,"score_gpt":0.22613640058675352,"score_spread":0.21714666628703497,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2017994263","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.98347324,0.0037010484,0.0020577966,0.0012254658,0.0001241969,0.00005869316,0.00019801802,0.00012597778,0.009035586],"genre_scores_gemma":[0.99486595,0.0013290544,0.0013977184,0.00011148249,0.00012856445,0.000018169414,0.00009548243,0.000010556616,0.0020429213],"study_design_codex":"case_report","study_design_gemma":"case_report","domain_scores_codex":[0.9998838,0.000032704647,0.00001553169,0.000019351413,0.000023946088,0.000024669558],"domain_scores_gemma":[0.9997727,0.00009218201,0.00005983571,0.000014762066,0.00001337386,0.00004720317],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00014337138,0.000405327,0.00030948225,0.0007917277,0.00031161154,0.00025417117,0.0003854741,0.0007275798,0.0023944424],"category_scores_gemma":[0.0008256638,0.0002494555,0.00015424524,0.00031812294,0.00051629345,0.00028577232,0.000507834,0.00049589504,0.00054140156],"study_design_candidate":"case_report","study_design_consensus":"case_report","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0020318378,0.00012332978,0.07136903,0.000317805,0.00008227499,0.7256217,0.00063824956,0.00094794895,0.15817101,0.011035803,0.001956985,0.027703943],"study_design_scores_gemma":[0.00018182471,0.000542058,0.10303725,0.00003885352,0.0002096351,0.83924586,0.00031184778,0.0012011612,0.035244934,0.0057913805,0.014159376,0.00003589346],"about_ca_topic_score_codex":0.0004729351,"about_ca_topic_score_gemma":0.00056713214,"teacher_disagreement_score":0.0023944424,"about_ca_system_score_codex":0.0002263191,"about_ca_system_score_gemma":0.00022756112,"threshold_uncertainty_score":0.008010209},"labels":[],"label_agreement":null},{"id":"W2019161989","doi":"10.1172/jci68035","title":"Loss-of-function mutations in SIM1 contribute to obesity and Prader-Willi–like features","year":2013,"lang":"en","type":"article","venue":"Journal of Clinical Investigation","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":147,"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","funders":"National Institute of Diabetes and Digestive and Kidney Diseases; Société Francophone du Diabète","keywords":"Haploinsufficiency; Obesity; Loss function; Internal medicine; Endocrinology; Biology; Gene; Genetics; Medicine; Phenotype","score_opus":0.03152585440061885,"score_gpt":0.32689034302281816,"score_spread":0.29536448862219933,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2019161989","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99874276,0.00017604232,0.00068628596,0.000020004973,0.0000038677094,0.000007354717,0.00013226521,0.000025135972,0.00020631134],"genre_scores_gemma":[0.99797195,0.00019445759,0.0011998726,0.000019523457,0.0000069060366,0.000009617177,0.00020973528,0.00001623192,0.00037171022],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9998461,0.000029468447,0.000018525405,0.00004313353,0.000040894985,0.00002188049],"domain_scores_gemma":[0.9997422,0.00006261502,0.0001240268,0.000016343047,0.000008629363,0.00004617836],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00014630916,0.0007557274,0.00021688663,0.000734387,0.0001885093,0.0001409984,0.00022123363,0.0003084945,0.0014878871],"category_scores_gemma":[0.00040622984,0.0002444807,0.0003546366,0.00029993386,0.0003758818,0.000080416,0.00038601135,0.00042931913,0.00023279554],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0008649317,0.00008497216,0.090388425,0.000095551535,0.0001717528,0.008928758,0.00021117234,0.0006220587,0.88973856,0.00030655778,0.00020653603,0.008380744],"study_design_scores_gemma":[0.0001305241,0.000706483,0.661654,0.00004385159,0.00027843946,0.04882663,0.00021918396,0.0039287033,0.27993354,0.00035448626,0.0038733566,0.000050778533],"about_ca_topic_score_codex":0.0005431416,"about_ca_topic_score_gemma":0.0009872683,"teacher_disagreement_score":0.0014878871,"about_ca_system_score_codex":0.00015052837,"about_ca_system_score_gemma":0.00012814852,"threshold_uncertainty_score":0.0049774647},"labels":[],"label_agreement":null},{"id":"W2019946659","doi":"10.1111/j.1399-0004.2010.01554.x","title":"Familial Simpson-Golabi-Behmel syndrome: studies of X-chromosome inactivation and clinical phenotypes in two female individuals with GPC3 mutations","year":2010,"lang":"en","type":"article","venue":"Clinical Genetics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","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":"Hospital for Sick Children","funders":"","keywords":"Macrocephaly; X-inactivation; Genetics; Skewed X-inactivation; X chromosome; Biology; Macroglossia; Mutation; Gene; Medicine; Pathology; Tongue","score_opus":0.044260759650186464,"score_gpt":0.391640784283223,"score_spread":0.3473800246330366,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2019946659","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9981047,0.00034730948,0.0003866537,0.00010037105,0.000020178988,0.000023184624,0.00011376122,0.000014701193,0.0008890826],"genre_scores_gemma":[0.9986701,0.00017403148,0.00029266503,0.00009438792,0.00003684561,0.000012430324,0.00010226686,0.000010176867,0.0006071406],"study_design_codex":"case_report","study_design_gemma":"case_report","domain_scores_codex":[0.9996401,0.000049056383,0.0000428235,0.000114915725,0.00007941373,0.000073767544],"domain_scores_gemma":[0.9994702,0.00012440681,0.00009497681,0.00003144606,0.00004230053,0.00023677485],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0002665368,0.001144572,0.0006478816,0.0015513572,0.00081615575,0.00039087728,0.0003570515,0.001363428,0.0025329273],"category_scores_gemma":[0.0013478538,0.00044155927,0.00044527973,0.0004716316,0.00065353024,0.00028466637,0.0007418451,0.00053476676,0.0004560652],"study_design_candidate":"case_report","study_design_consensus":"case_report","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0004300644,0.0002405853,0.19116783,0.000061781706,0.00006307268,0.7625627,0.0027747005,0.00013037879,0.035378646,0.00033152397,0.00037123825,0.006487532],"study_design_scores_gemma":[0.000043919154,0.00044677476,0.16157666,0.000010952994,0.00003713759,0.83290213,0.0003541883,0.00023684802,0.0030140162,0.00011415035,0.0012368271,0.00002647748],"about_ca_topic_score_codex":0.0015059493,"about_ca_topic_score_gemma":0.0008480695,"teacher_disagreement_score":0.0025329273,"about_ca_system_score_codex":0.00030250553,"about_ca_system_score_gemma":0.00020803043,"threshold_uncertainty_score":0.0084735155},"labels":[],"label_agreement":null},{"id":"W2020816946","doi":"10.3389/fgene.2015.00058","title":"Epigenetic consequences of artificial reproductive technologies to the bovine imprinted genes SNRPN, H19/IGF2, and IGF2R","year":2015,"lang":"en","type":"article","venue":"Frontiers in Genetics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","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","funders":"","keywords":"Genomic imprinting; Epigenetics; Biology; Genetics; Reproductive technology; Somatic cell; Offspring; Imprinting (psychology); DNA methylation; Gene; Computational biology; Gene expression; Pregnancy; Embryogenesis","score_opus":0.018855963081406184,"score_gpt":0.2514591098466592,"score_spread":0.232603146765253,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2020816946","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9662193,0.013229926,0.014204168,0.00035278779,0.00013783584,0.000016344242,0.0003273987,0.00009818131,0.005414083],"genre_scores_gemma":[0.99081814,0.0045638625,0.0019888207,0.0001547551,0.00003147286,0.000012463527,0.00021427848,0.00002326549,0.0021930411],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99973947,0.00009519639,0.000020668951,0.000046688314,0.00007339599,0.000024605148],"domain_scores_gemma":[0.9996762,0.00013354277,0.00012586909,0.00002572385,0.00001942277,0.00001925718],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00034181555,0.00015449089,0.00012122208,0.00024615938,0.000119758115,0.0002104823,0.00021175227,0.00020969246,0.0011589007],"category_scores_gemma":[0.0005579293,0.00007856942,0.0001944466,0.00019682154,0.00041037038,0.00013529367,0.00020864702,0.0002396921,0.00012382586],"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":[0.0002365748,0.000028357601,0.009691005,0.00018881436,0.0001004449,0.0016952648,0.00014313438,0.0005324258,0.94675475,0.0024286918,0.00019561744,0.038004946],"study_design_scores_gemma":[0.000030265066,0.0008187954,0.13569115,0.000057266025,0.00032878856,0.008665099,0.00023886618,0.0017209047,0.8294975,0.002044307,0.020877222,0.000029797127],"about_ca_topic_score_codex":0.00047599542,"about_ca_topic_score_gemma":0.00062701805,"teacher_disagreement_score":0.0011589007,"about_ca_system_score_codex":0.00023548312,"about_ca_system_score_gemma":0.00012807497,"threshold_uncertainty_score":0.003876865},"labels":[],"label_agreement":null},{"id":"W2021120315","doi":"10.1210/en.2005-1487","title":"Coding<i>GNAS</i>Mutations Leading to Hormone Resistance Impair<i>in Vitro</i>Agonist- and Cholera Toxin-Induced Adenosine Cyclic 3′,5′-Monophosphate Formation Mediated by Human XLαs","year":2006,"lang":"en","type":"article","venue":"Endocrinology","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":56,"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; Royal Victoria Hospital; Royal Victoria Regional Health Centre","funders":"National Institute of Diabetes and Digestive and Kidney Diseases; U.S. Public Health Service","keywords":"GNAS complex locus; Gs alpha subunit; Cholera toxin; G protein-coupled receptor; Endocrinology; Internal medicine; Biology; Receptor; Pseudohypoparathyroidism; Signal transduction; Wild type; G protein; Cell biology; Mutant; Parathyroid hormone; Biochemistry; Medicine; Calcium; Gene","score_opus":0.008624274444104416,"score_gpt":0.2448305225797903,"score_spread":0.2362062481356859,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2021120315","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.996781,0.00020611218,0.0014664541,0.000049468235,0.000019521221,0.000018531298,0.00046363653,0.00005958388,0.0009357377],"genre_scores_gemma":[0.99464285,0.00025272477,0.0014789522,0.000042554195,0.000009521294,0.000019046194,0.0013024185,0.000037790345,0.002214141],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99988604,0.000018849429,0.000016281085,0.000024507297,0.000028552673,0.000025713745],"domain_scores_gemma":[0.99985874,0.000023594219,0.000052948864,0.000021114716,0.000007175861,0.000036513622],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00008815712,0.0004581633,0.00011878173,0.0001325409,0.00010281593,0.00023307673,0.00017943881,0.0002046411,0.0020237379],"category_scores_gemma":[0.000108771026,0.00012352513,0.00024187144,0.00013116606,0.00030444664,0.00011293793,0.00017391123,0.00041917132,0.00068389036],"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":[0.000063576386,0.000011437013,0.00014915434,0.0000074156105,0.0000030007238,0.00009447935,0.000007836421,0.000034334887,0.9992219,0.00007791645,0.000019230229,0.00030974895],"study_design_scores_gemma":[0.000033340686,0.00018756418,0.005918506,0.000005343965,0.000013223212,0.0011428342,0.000045423618,0.0008178782,0.9891917,0.00005109911,0.002588072,0.0000050233416],"about_ca_topic_score_codex":0.0010283794,"about_ca_topic_score_gemma":0.0010890882,"teacher_disagreement_score":0.0020237379,"about_ca_system_score_codex":0.0002993297,"about_ca_system_score_gemma":0.00015696141,"threshold_uncertainty_score":0.0067700148},"labels":[],"label_agreement":null},{"id":"W2021178751","doi":"10.1016/j.mehy.2004.05.010","title":"Just how happy is the happy puppet? An emotion signaling and kinship theory perspective on the behavioral phenotype of children with Angelman syndrome","year":2004,"lang":"en","type":"article","venue":"Medical Hypotheses","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":62,"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 General Medical Sciences; Natural Sciences and Engineering Research Council of Canada; National Institute on Aging; National Institutes of Health","keywords":"Genomic imprinting; Angelman syndrome; Genetics; Phenotype; Biology; Kinship; UBE3A; Gene; Imprinting (psychology); Developmental psychology; Psychology; Gene expression; DNA methylation","score_opus":0.026931989710451867,"score_gpt":0.2631787664788764,"score_spread":0.23624677676842454,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2021178751","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.89098257,0.00641174,0.01497782,0.0515024,0.00029288503,0.000016172264,0.00016301444,0.00008200368,0.035571378],"genre_scores_gemma":[0.9930661,0.0022183065,0.0021208995,0.0007334685,0.00009231496,0.000010362016,0.000028536297,0.000008293488,0.0017215911],"study_design_codex":"theoretical_or_conceptual","study_design_gemma":"observational","domain_scores_codex":[0.99982697,0.00005757198,0.000007473527,0.000030160827,0.000043495635,0.000034362427],"domain_scores_gemma":[0.99970144,0.00015418782,0.00007124648,0.000015551073,0.000021909396,0.00003560308],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00043326354,0.00047845393,0.00042925202,0.0005675704,0.00045396874,0.0007995303,0.0006149166,0.00094487827,0.0013204908],"category_scores_gemma":[0.0009924414,0.00014275573,0.0001891591,0.0003031433,0.004568776,0.0011835876,0.00063704216,0.0013473211,0.0001083591],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00037294184,0.00011700063,0.05410643,0.00023130825,0.00010535837,0.03465814,0.012877669,0.0034594408,0.093047135,0.7468678,0.0041271998,0.05002971],"study_design_scores_gemma":[0.00012665088,0.00060608215,0.17645197,0.00032567128,0.00024573875,0.07200693,0.040728208,0.008720287,0.03983037,0.6318378,0.028878251,0.00024192361],"about_ca_topic_score_codex":0.0014245429,"about_ca_topic_score_gemma":0.0016328737,"teacher_disagreement_score":0.0014245429,"about_ca_system_score_codex":0.00052197475,"about_ca_system_score_gemma":0.00043364574,"threshold_uncertainty_score":0.004417479},"labels":[],"label_agreement":null},{"id":"W2021548102","doi":"10.1016/j.jpeds.2008.07.058","title":"Retrospective Study of the Potential Benefits and Adverse Events during Growth Hormone Treatment in Children with Prader-Willi Syndrome","year":2008,"lang":"en","type":"article","venue":"The Journal of Pediatrics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":49,"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":"Medicine; Body mass index; Growth hormone; Internal medicine; Pediatrics; Adverse effect; Endocrinology; Obstructive sleep apnea; Hormone; Gastroenterology","score_opus":0.005606803000168144,"score_gpt":0.1931648111970808,"score_spread":0.18755800819691265,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2021548102","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99931276,0.00018168254,0.000056264482,0.000011204451,0.0000029030457,0.0000066776065,0.0001510515,0.0000020806317,0.00027546578],"genre_scores_gemma":[0.9994929,0.00013398103,0.00007240207,0.000019290903,0.00000894364,0.0000071992918,0.00019302248,0.0000019800527,0.00007027255],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9994093,0.00015487833,0.00011215279,0.00011208062,0.000110621964,0.00010099051],"domain_scores_gemma":[0.99729174,0.0008508415,0.0010445463,0.00016545778,0.00019342829,0.00045399662],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0004543092,0.00028937598,0.00039153028,0.0010720688,0.0005740988,0.00038097892,0.00022013129,0.00046446535,0.0007730279],"category_scores_gemma":[0.0024223502,0.00021925382,0.0005569062,0.0009809401,0.0004868625,0.0002877937,0.0003541283,0.0006867102,0.00014644553],"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":[0.00028142688,0.000058209185,0.9961825,0.000012260668,0.000029661467,0.0018776434,0.00014947052,0.00006869427,0.00033089364,0.000023328916,0.00002949656,0.00095635507],"study_design_scores_gemma":[0.000009542265,0.0009015168,0.9898839,0.000004991125,0.000057956768,0.007944232,0.0004546793,0.00011977673,0.00029759976,0.000025080459,0.00028934478,0.000011394507],"about_ca_topic_score_codex":0.0038424565,"about_ca_topic_score_gemma":0.0028738135,"teacher_disagreement_score":0.0038424565,"about_ca_system_score_codex":0.0005166875,"about_ca_system_score_gemma":0.00051325915,"threshold_uncertainty_score":0.007640183},"labels":[],"label_agreement":null},{"id":"W2022030369","doi":"10.1155/2012/585024","title":"Epigenetic Mechanisms of Genomic Imprinting: Common Themes in the Regulation of Imprinted Regions in Mammals, Plants, and Insects","year":2012,"lang":"en","type":"article","venue":"Genetics Research International","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":87,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Children’s Health Research Institute; Dalhousie University; Western University","funders":"Natural Sciences and Engineering Research Council of Canada; Mount Allison University; Dalhousie University; Nova Scotia Health Research Foundation","keywords":"Genomic imprinting; Epigenetics; Imprinting (psychology); Biology; DNA methylation; Genetics; Gene; Locus (genetics); Regulation of gene expression; Gene expression","score_opus":0.05222290356522752,"score_gpt":0.34007468910862443,"score_spread":0.2878517855433969,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2022030369","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":[0.0817108,0.85561156,0.041320536,0.003115437,0.00040591147,0.000059142083,0.0002895868,0.00020818529,0.017278833],"genre_scores_gemma":[0.35118872,0.61728495,0.020890942,0.0012216944,0.0007671373,0.0000739709,0.00031388082,0.000047171514,0.008211598],"study_design_codex":"bench_or_experimental","study_design_gemma":"theoretical_or_conceptual","domain_scores_codex":[0.99981123,0.000027023425,0.0000180819,0.000052967964,0.000064715816,0.00002595966],"domain_scores_gemma":[0.9998796,0.000037673115,0.000040492123,0.000010618005,0.000015356152,0.000016210455],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0004385068,0.00034176148,0.0006468019,0.0008420652,0.00046111178,0.0010669861,0.0004647567,0.00058183924,0.00075686903],"category_scores_gemma":[0.00023135949,0.00017858623,0.00035105503,0.0010427173,0.0015295008,0.0011812065,0.00063490827,0.00091112667,0.00022803308],"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":[0.00032727545,0.00006264679,0.0067324736,0.0042680427,0.00021138373,0.004507054,0.003999416,0.0020970851,0.45129985,0.093180045,0.002425014,0.4308898],"study_design_scores_gemma":[0.000056101715,0.00086887274,0.10959145,0.0015460266,0.0005220826,0.025135385,0.0035415725,0.002380245,0.24861395,0.121673174,0.48578352,0.0002876463],"about_ca_topic_score_codex":0.00064710306,"about_ca_topic_score_gemma":0.0010929409,"teacher_disagreement_score":0.0010669861,"about_ca_system_score_codex":0.0005904031,"about_ca_system_score_gemma":0.00029681952,"threshold_uncertainty_score":0.0042836666},"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":"W2022617739","doi":"10.1159/000133150","title":"Mapping of the gene coding for the muscle protein nebulin (Neb) to the proximal region of mouse Chromosome 2","year":2008,"lang":"en","type":"article","venue":"Cytogenetics and Cell Genetics","topic":"Genetic Syndromes and Imprinting","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":"McGill University; McGill University Health Centre; Montreal General Hospital","funders":"","keywords":"Biology; Molecular biology; Genetics; Gene; Chromosome","score_opus":0.023713547358050008,"score_gpt":0.21810274760076617,"score_spread":0.19438920024271616,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2022617739","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9804647,0.002112185,0.013087637,0.00008631182,0.000026410597,0.00014960396,0.0007298576,0.00013360564,0.0032096037],"genre_scores_gemma":[0.9584908,0.0034676974,0.02296741,0.00015595778,0.000059546164,0.00018146714,0.0064996015,0.00015377229,0.008023741],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9995747,0.000058142305,0.000027784328,0.00015943556,0.00012323444,0.00005671247],"domain_scores_gemma":[0.99948126,0.0001808115,0.00015473105,0.00006487591,0.00003008316,0.00008830278],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00039322738,0.00073568715,0.00045677918,0.0020781376,0.00032175693,0.00032704725,0.0008795727,0.0005021421,0.002695539],"category_scores_gemma":[0.00048037348,0.0005294093,0.00070925866,0.00053319277,0.00065989065,0.00015277517,0.00075763935,0.00093014946,0.0008304086],"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":[0.0001736208,0.000054350912,0.0013827672,0.00005801017,0.000032320793,0.00025801716,0.000055205393,0.00017732498,0.9916619,0.00032630333,0.000031612093,0.0057886494],"study_design_scores_gemma":[0.0002924067,0.0015200295,0.11318788,0.00014309556,0.00041196335,0.004398422,0.00009884612,0.0019917474,0.8630497,0.00048315673,0.014363221,0.00005960396],"about_ca_topic_score_codex":0.0024891673,"about_ca_topic_score_gemma":0.003706707,"teacher_disagreement_score":0.002695539,"about_ca_system_score_codex":0.00043133806,"about_ca_system_score_gemma":0.0004271216,"threshold_uncertainty_score":0.0090174675},"labels":[],"label_agreement":null},{"id":"W2022971808","doi":"10.1016/j.jpeds.2012.07.042","title":"Longitudinal Evaluation of Sleep-Disordered Breathing in Children with Prader-Willi Syndrome during 2 Years of Growth Hormone Therapy","year":2012,"lang":"en","type":"article","venue":"The Journal of Pediatrics","topic":"Genetic Syndromes and Imprinting","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":"University Health Network; Toronto Western Hospital; Hospital for Sick Children; University of Toronto","funders":"","keywords":"Medicine; Polysomnography; Pediatrics; Context (archaeology); Obstructive sleep apnea; Sleep disordered breathing; Sleep apnea; Body mass index; Apnea; Growth hormone; Internal medicine; Hormone","score_opus":0.013658074120025595,"score_gpt":0.24225123566068635,"score_spread":0.22859316154066076,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2022971808","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9993337,0.00017494663,0.00004433302,0.000031288288,0.000005010634,0.000009448798,0.0001864972,0.000004606452,0.00021011101],"genre_scores_gemma":[0.9990312,0.00013108803,0.00007025696,0.000022628747,0.000007651903,0.000016789061,0.00052438414,0.00000236702,0.00019361051],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9994267,0.0001369234,0.00007340579,0.000101397505,0.00009902389,0.00016264584],"domain_scores_gemma":[0.9979686,0.0003570728,0.0006913091,0.000080682716,0.00033810714,0.00056422036],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0008702327,0.00041379352,0.000597114,0.0016319263,0.00084401644,0.0007338092,0.00046541952,0.0007765838,0.0004775904],"category_scores_gemma":[0.0030061002,0.00032240976,0.00086473057,0.0009885333,0.00037612158,0.0007521753,0.00071853667,0.0009837825,0.00021400301],"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":[0.00022040858,0.00008515046,0.997696,0.00000423999,0.000024841243,0.0004526676,0.00023941856,0.000039058854,0.0004545353,0.000005943222,0.000026046117,0.000751633],"study_design_scores_gemma":[0.0000038916423,0.00031504157,0.9984841,0.0000029432135,0.0000224478,0.0005865509,0.0002853975,0.00007285333,0.00011341539,0.000005510138,0.000101974176,0.0000058738574],"about_ca_topic_score_codex":0.015973184,"about_ca_topic_score_gemma":0.014099343,"teacher_disagreement_score":0.015973184,"about_ca_system_score_codex":0.0006886711,"about_ca_system_score_gemma":0.0008127649,"threshold_uncertainty_score":0.031760395},"labels":[],"label_agreement":null},{"id":"W2023174704","doi":"10.1371/journal.pone.0004291","title":"Loss of Magel2, a Candidate Gene for Features of Prader-Willi Syndrome, Impairs Reproductive Function in Mice","year":2009,"lang":"en","type":"article","venue":"PLoS ONE","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":99,"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":"Natural Sciences and Engineering Research Council of Canada; Canadian Institutes of Health Research; University of California, San Diego; University of Alberta; Canadian Diabetes Association","keywords":"Loss function; Gene; Function (biology); Genetics; Candidate gene; Biology; Medicine; Internal medicine; Endocrinology; Phenotype","score_opus":0.013706530261128185,"score_gpt":0.22517955467328649,"score_spread":0.2114730244121583,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2023174704","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9902575,0.00077763293,0.005605115,0.00020062093,0.000045192755,0.000034516583,0.0014919372,0.0003608034,0.0012266538],"genre_scores_gemma":[0.9869175,0.0007275896,0.0056858254,0.00010772594,0.000024574094,0.00008544259,0.0012395255,0.00012424865,0.0050876257],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9998579,0.00002060845,0.000015462832,0.000045949368,0.0000364894,0.000023555935],"domain_scores_gemma":[0.9997522,0.00004614277,0.00010226058,0.000020401192,0.000008898481,0.00007005802],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00018475039,0.00072498503,0.00022204682,0.000942207,0.00018601157,0.00023079569,0.0004811752,0.00058221625,0.0038940571],"category_scores_gemma":[0.00020634336,0.0002763868,0.00040960242,0.00021955025,0.00043918245,0.00020849686,0.00036712884,0.0007309062,0.00069287536],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00023716177,0.00004332221,0.0009985274,0.000037517606,0.000021287435,0.0006066158,0.000026178124,0.00013202269,0.99571425,0.00022893988,0.00011958509,0.0018346919],"study_design_scores_gemma":[0.00018221089,0.0006788873,0.034385208,0.000029221297,0.00012539365,0.006916444,0.00008214964,0.0029868523,0.9479267,0.0003121174,0.006346801,0.000028027122],"about_ca_topic_score_codex":0.00032406492,"about_ca_topic_score_gemma":0.00067840476,"teacher_disagreement_score":0.0038940571,"about_ca_system_score_codex":0.0002083526,"about_ca_system_score_gemma":0.00018338808,"threshold_uncertainty_score":0.013026953},"labels":[],"label_agreement":null},{"id":"W2023332321","doi":"10.1002/ajmg.a.31274","title":"Overgrowth with severe developmental delay following IVF/ICSI: A newly recognized syndrome?","year":2006,"lang":"en","type":"article","venue":"American Journal of Medical Genetics Part A","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":12,"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; University of Toronto; SickKids Foundation; Mount Sinai Hospital","funders":"","keywords":"Intracytoplasmic sperm injection; In vitro fertilisation; Medicine; Global developmental delay; Pathogenesis; Genomic imprinting; Pregnancy; Pediatrics; Biology; Internal medicine; Genetics; Phenotype","score_opus":0.005980403779854638,"score_gpt":0.2294149075923145,"score_spread":0.22343450381245986,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2023332321","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9916142,0.0022403938,0.0016894334,0.0012861557,0.00013320192,0.00004300186,0.00017190233,0.00011723447,0.0027044537],"genre_scores_gemma":[0.99567235,0.0017711889,0.0014057286,0.00027676031,0.00021036911,0.00002174411,0.000089276335,0.000017624203,0.00053492904],"study_design_codex":"case_report","study_design_gemma":"case_report","domain_scores_codex":[0.9997849,0.00003150045,0.000024421555,0.000056291603,0.000042161948,0.00006070064],"domain_scores_gemma":[0.99910456,0.00030434353,0.00033397527,0.00003970109,0.000030550575,0.00018675109],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0001600944,0.0015459313,0.0006236432,0.00073230057,0.00089505425,0.0005105676,0.0005485067,0.0014206716,0.0011231396],"category_scores_gemma":[0.001605313,0.00036684054,0.00039762305,0.0007548979,0.0012375979,0.00039363845,0.0008577323,0.0011242144,0.00026752363],"study_design_candidate":"case_report","study_design_consensus":"case_report","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.000064958476,0.000024632824,0.013378383,0.000035595633,0.000015059669,0.97891515,0.00022385671,0.000083343846,0.0036937313,0.00019155607,0.0002312329,0.0031425036],"study_design_scores_gemma":[0.0000132125915,0.000083461564,0.011308902,0.0000072609846,0.000020374173,0.98705393,0.00007080622,0.000096763935,0.0007057846,0.000115118746,0.0005174241,0.000006906624],"about_ca_topic_score_codex":0.0011675768,"about_ca_topic_score_gemma":0.0021333038,"teacher_disagreement_score":0.0015459313,"about_ca_system_score_codex":0.00026617447,"about_ca_system_score_gemma":0.0003872108,"threshold_uncertainty_score":0.0037572384},"labels":[],"label_agreement":null},{"id":"W2023847394","doi":"10.1016/j.placenta.2009.07.007","title":"Unearthing the Roles of Imprinted Genes in the Placenta","year":2009,"lang":"en","type":"review","venue":"Placenta","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":92,"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":"Genomic imprinting; Epigenetics; Biology; Placentation; Placenta; Conceptus; Imprinting (psychology); Genetics; Gene; Phenotype; Epigenesis; Embryo; DNA methylation; Fetus; Gene expression; Pregnancy","score_opus":0.026513536937667708,"score_gpt":0.3024756736617026,"score_spread":0.27596213672403486,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2023847394","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":[0.000064856096,0.99895203,0.00012721395,0.00034767148,0.00016149618,9.069695e-7,0.0000070110204,0.0000029087835,0.00033586082],"genre_scores_gemma":[0.00036073077,0.99874735,0.00013402621,0.00018335746,0.00029654222,0.0000014638633,0.000010837436,7.925334e-7,0.00026485714],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.9997316,0.000043311848,0.000044317312,0.000054732718,0.00010397752,0.000022045055],"domain_scores_gemma":[0.9992435,0.0004281594,0.00007094067,0.000029988763,0.0001720438,0.000055376408],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0010176508,0.000854401,0.0018848062,0.0020573882,0.00032816446,0.0015485657,0.0013476163,0.0018478368,0.0015278995],"category_scores_gemma":[0.0013736122,0.00048848067,0.00038521088,0.002481389,0.0014853907,0.0021754731,0.0009870342,0.0026813387,0.001310406],"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":[0.00013651852,0.000038695187,0.0004108377,0.009806478,0.00010708943,0.0009152763,0.00009781926,0.000620025,0.0051391684,0.011183521,0.04287452,0.92867005],"study_design_scores_gemma":[0.000018479117,0.00003829035,0.0009085454,0.0019150856,0.00010069526,0.0030258922,0.00011562508,0.00011835498,0.0009403042,0.006311447,0.9864798,0.000027501657],"about_ca_topic_score_codex":0.0022523508,"about_ca_topic_score_gemma":0.00292273,"teacher_disagreement_score":0.0022523508,"about_ca_system_score_codex":0.0011749611,"about_ca_system_score_gemma":0.001577933,"threshold_uncertainty_score":0.008524954},"labels":[],"label_agreement":null},{"id":"W2024054703","doi":"10.1016/s0893-133x(00)00127-5","title":"The Genes for Major Psychosis Aberrant Sequence or Regulation?","year":2000,"lang":"en","type":"review","venue":"Neuropsychopharmacology","topic":"Genetic Syndromes and Imprinting","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":"Centre for Addiction and Mental Health; University of Toronto","funders":"National Alliance for Research on Schizophrenia and Depression","keywords":"Epigenetics; Genetics; Genomic imprinting; Biology; DNA methylation; Psychosis; Bipolar disorder; Allele; Genetic association; Gene; Genotype; Psychology; Neuroscience; Psychiatry; Single-nucleotide polymorphism; Gene expression","score_opus":0.0546937931192884,"score_gpt":0.380805176764032,"score_spread":0.3261113836447436,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2024054703","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":[0.0006599152,0.992942,0.0006917171,0.0026002945,0.00070292066,0.00000544672,0.000040934206,0.000024070981,0.0023328126],"genre_scores_gemma":[0.005444486,0.9890956,0.0007361936,0.0013873426,0.00083103136,0.000016184662,0.0000635735,0.0000040620953,0.00242146],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.9999107,0.000023113089,0.000011751879,0.000018103337,0.000022052978,0.000014192233],"domain_scores_gemma":[0.9998634,0.00007267863,0.000019301184,0.000008756692,0.000021225615,0.000014578721],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0004451066,0.0008363301,0.0012550636,0.0007654732,0.00021395466,0.0009049761,0.0011995358,0.0016256789,0.002223114],"category_scores_gemma":[0.00051819603,0.00024124085,0.00023602687,0.00092398666,0.0012160752,0.0013358683,0.00038226385,0.001601681,0.0013939197],"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":[0.00035512142,0.000068111854,0.0014298488,0.0046383003,0.0001354699,0.0044049523,0.00018127583,0.00085412257,0.019128188,0.032065067,0.07676618,0.8599733],"study_design_scores_gemma":[0.00010445767,0.00007747968,0.0029090538,0.0012944661,0.00011997702,0.012479004,0.0003619171,0.000267092,0.0033284563,0.03191163,0.9470983,0.000047989637],"about_ca_topic_score_codex":0.0010259681,"about_ca_topic_score_gemma":0.001714529,"teacher_disagreement_score":0.002223114,"about_ca_system_score_codex":0.000700118,"about_ca_system_score_gemma":0.0007180698,"threshold_uncertainty_score":0.0074370503},"labels":[],"label_agreement":null},{"id":"W2024184784","doi":"10.1007/s11695-011-0503-1","title":"Reply to the Letter of Scheimann et al.","year":2011,"lang":"en","type":"letter","venue":"Obesity Surgery","topic":"Genetic Syndromes and Imprinting","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":"Université Laval","funders":"","keywords":"Medicine; General surgery","score_opus":0.02141018257372177,"score_gpt":0.2324022489736346,"score_spread":0.21099206639991283,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2024184784","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":[0.00036879902,0.0018141675,0.00005366355,0.97694266,0.019751566,0.0000068729964,0.00004975426,0.000023468541,0.0009889462],"genre_scores_gemma":[0.0042608776,0.0016746328,0.00015319722,0.9551522,0.034583334,0.00003031496,0.000042710686,0.000025638426,0.0040771035],"study_design_codex":"not_applicable","study_design_gemma":"not_applicable","domain_scores_codex":[0.99860954,0.0004721325,0.00016154247,0.000200703,0.00034021316,0.00021579467],"domain_scores_gemma":[0.9960439,0.0022692,0.0002916806,0.00012442889,0.00071426155,0.0005565588],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0021620165,0.0008805131,0.0013818213,0.0007393633,0.002799747,0.0024956486,0.0018683384,0.03934474,0.004917804],"category_scores_gemma":[0.017927643,0.0006853228,0.00087647885,0.00068134506,0.002365082,0.0034746593,0.0012813585,0.030358173,0.0050347876],"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":[0.0000783775,0.000019589239,0.00043378162,0.000039599323,0.0000118684275,0.0020750551,0.000080113685,0.00004110361,0.00009281535,0.0007496476,0.9926536,0.0037244176],"study_design_scores_gemma":[0.00023589864,0.0001384727,0.002028697,0.00037817124,0.00006801342,0.010435018,0.0007902455,0.0006461429,0.00064039323,0.010336921,0.9741509,0.00015102826],"about_ca_topic_score_codex":0.0032750475,"about_ca_topic_score_gemma":0.004299535,"teacher_disagreement_score":0.03934474,"about_ca_system_score_codex":0.0024911691,"about_ca_system_score_gemma":0.0019761408,"threshold_uncertainty_score":0.01807481},"labels":[],"label_agreement":null},{"id":"W2024495278","doi":"10.1139/o03-052","title":"The many roles of the transcriptional regulator CTCF","year":2003,"lang":"en","type":"review","venue":"Biochemistry and Cell Biology","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":67,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":true,"route_about_ca":false,"ca_institutions":"University of Manitoba","funders":"","keywords":"CTCF; Regulator; Imprinting (psychology); Transcriptional regulation; Biology; Genetics; Psychological repression; Gene; Insulator (electricity); Regulation of gene expression; YY1; Transcription factor; Mechanism (biology); Function (biology); Repressor; Computational biology; Cell biology; Gene expression; Promoter; Enhancer","score_opus":0.01213321326155398,"score_gpt":0.24364173381532198,"score_spread":0.231508520553768,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2024495278","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":[0.0002279658,0.9966577,0.00041150273,0.00037340063,0.00022023717,0.000002846389,0.000013098886,0.000010652244,0.0020825644],"genre_scores_gemma":[0.0016256755,0.99611974,0.0002848124,0.00022399526,0.0001870794,0.000005832106,0.000031984335,0.0000021638452,0.0015186807],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.99986434,0.000021386662,0.000013065241,0.00003353763,0.000052234456,0.0000154413],"domain_scores_gemma":[0.9998313,0.00006374477,0.00001967472,0.000010087704,0.000049325732,0.000025786843],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00047105562,0.00064186857,0.00082250003,0.0011225032,0.00023711767,0.00091555883,0.00093473814,0.000870649,0.0016870069],"category_scores_gemma":[0.00048466565,0.00022324028,0.00019331912,0.001266205,0.00065838237,0.0009803814,0.0005357037,0.0012785632,0.002415635],"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":[0.000063456806,0.000024429713,0.0001946352,0.0037548759,0.00002963153,0.00027765895,0.000070178816,0.00035491874,0.008258467,0.0074820863,0.023247238,0.9562423],"study_design_scores_gemma":[0.000008284177,0.000025303763,0.000493962,0.0005595317,0.00001635015,0.0008970125,0.00003822332,0.000048264003,0.0014687339,0.0023920503,0.9940432,0.000009158544],"about_ca_topic_score_codex":0.00095465436,"about_ca_topic_score_gemma":0.0011760679,"teacher_disagreement_score":0.0016870069,"about_ca_system_score_codex":0.0007446344,"about_ca_system_score_gemma":0.00069394003,"threshold_uncertainty_score":0.005643666},"labels":[],"label_agreement":null},{"id":"W2024628398","doi":"10.1139/o11-043","title":"Setting up and maintaining differential insulators and boundaries for genomic imprinting","year":2011,"lang":"en","type":"review","venue":"Biochemistry and Cell Biology","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":20,"is_retracted":false,"has_abstract":true,"route_ca_aff":false,"route_ca_fund":false,"route_ca_venue":true,"route_about_ca":false,"ca_institutions":"","funders":"Cancer Research UK","keywords":"CTCF; Chromatin; Genomic imprinting; Biology; Insulator (electricity); Epigenetics; Gene; Genetics; Genome; Locus (genetics); Imprinting (psychology); Genomic organization; Somatic cell; Regulation of gene expression; Transcription factor; Computational biology; DNA methylation; Gene expression; Enhancer","score_opus":0.015561035741652915,"score_gpt":0.2599823396318963,"score_spread":0.2444213038902434,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2024628398","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":[0.00030521976,0.9978091,0.0002757152,0.00015607993,0.000107023545,0.0000035405938,0.000015402067,0.00001098049,0.0013169463],"genre_scores_gemma":[0.0012476466,0.99750745,0.00037433126,0.00008800603,0.00007492368,0.000006161599,0.00002625257,0.0000021920298,0.00067296246],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.99987197,0.000019148332,0.000016982744,0.000025688973,0.000050204646,0.000016086697],"domain_scores_gemma":[0.9998816,0.0000471335,0.000023547644,0.0000048413654,0.000026985872,0.000015877617],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.000371773,0.00067317806,0.0012899381,0.0015123572,0.00023952214,0.00081459014,0.00072213,0.0010722133,0.0019694571],"category_scores_gemma":[0.00031134725,0.00027021754,0.00026502553,0.0014104089,0.0007207374,0.0012601442,0.000553092,0.0010713,0.0026031516],"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":[0.00007395121,0.00005155138,0.0002673391,0.016468132,0.000056424604,0.00046547063,0.0001094024,0.00044639304,0.01278659,0.009647733,0.01480789,0.94481915],"study_design_scores_gemma":[0.000014494382,0.00006190356,0.0010121934,0.0012620905,0.000052556567,0.001735559,0.00008961702,0.00006636389,0.0031353168,0.0029302267,0.98962116,0.000018487099],"about_ca_topic_score_codex":0.00078738865,"about_ca_topic_score_gemma":0.001194668,"teacher_disagreement_score":0.0019694571,"about_ca_system_score_codex":0.0006376028,"about_ca_system_score_gemma":0.00072572636,"threshold_uncertainty_score":0.0065885186},"labels":[],"label_agreement":null},{"id":"W2024673645","doi":"10.1016/s0002-9440(10)62964-1","title":"Developmental Abnormalities of Neuronal Structure and Function in Prenatal Mice Lacking the Prader-Willi Syndrome Gene Necdin","year":2005,"lang":"en","type":"article","venue":"American Journal Of Pathology","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":98,"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","funders":"Canadian Institutes of Health Research; Fondation pour la Recherche Médicale","keywords":"Gene; Biology; Genetics; Medicine; Endocrinology; Internal medicine; Pathology","score_opus":0.005945838220352216,"score_gpt":0.2127885638113434,"score_spread":0.20684272559099118,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2024673645","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99550843,0.00056582416,0.001943264,0.000113563816,0.00002675299,0.000009643107,0.0004585226,0.00013635056,0.0012376233],"genre_scores_gemma":[0.99142563,0.000699123,0.0030036133,0.000041991403,0.000008606013,0.000020184254,0.00034176576,0.00009487136,0.004364155],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99973875,0.000033009906,0.000030723288,0.000062254985,0.00009643566,0.000038865957],"domain_scores_gemma":[0.99944896,0.00012592271,0.00021439242,0.00005533795,0.000038174614,0.00011732195],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00015279005,0.0005329087,0.0002511499,0.00078344665,0.00020192987,0.00034658337,0.00039104928,0.0005645386,0.0019439971],"category_scores_gemma":[0.00036185386,0.00049768767,0.00018078797,0.00015451963,0.0005781612,0.00029784598,0.00036202002,0.0010162212,0.00037050314],"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":[0.00017872757,0.00002097158,0.00041261833,0.000019883406,0.000007475031,0.0004791965,0.000034751334,0.00014087814,0.9971692,0.0003927622,0.000038911297,0.0011045779],"study_design_scores_gemma":[0.0000622926,0.00021389622,0.023805305,0.00002034691,0.000050461673,0.0034527406,0.0000847071,0.0012145201,0.9690579,0.00028909813,0.001732775,0.000015912852],"about_ca_topic_score_codex":0.0012730645,"about_ca_topic_score_gemma":0.0021937182,"teacher_disagreement_score":0.0019439971,"about_ca_system_score_codex":0.00044236248,"about_ca_system_score_gemma":0.0003296344,"threshold_uncertainty_score":0.0065033436},"labels":[],"label_agreement":null},{"id":"W2024727939","doi":"10.1016/j.fertnstert.2015.03.020","title":"Deoxyribonucleic acid methylation profiling of single human blastocysts by methylated CpG-island amplification coupled with CpG-island microarray","year":2015,"lang":"en","type":"article","venue":"Fertility and Sterility","topic":"Genetic Syndromes and Imprinting","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":"Princess Margaret Cancer Centre","funders":"Society for Reproduction and Fertility; Medical Research Council; Newlife the Charity for Disabled Children","keywords":"DNA methylation; Differentially methylated regions; CpG site; Biology; Methylation; Blastocyst; Microarray; Methylated DNA immunoprecipitation; Molecular biology; Genetics; DNA microarray; Embryo; DNA; Gene; Embryogenesis; Gene expression","score_opus":0.023678935345627126,"score_gpt":0.2528869824133242,"score_spread":0.22920804706769707,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2024727939","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9229406,0.0014715558,0.07003956,0.00013379093,0.000024818108,0.00038680254,0.0021459714,0.00027987314,0.0025771055],"genre_scores_gemma":[0.9148564,0.0008514449,0.078931734,0.00010027455,0.000014299803,0.00044883313,0.0018378041,0.00004000509,0.0029192732],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99968684,0.00006302576,0.000019549436,0.00011250824,0.0000918842,0.000026274849],"domain_scores_gemma":[0.9998317,0.000066745444,0.000029220666,0.000022899982,0.00003211038,0.000017425175],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00046359395,0.0002642837,0.0003455346,0.0004212702,0.00017459443,0.0002094371,0.000264051,0.00037694984,0.00153286],"category_scores_gemma":[0.0006739329,0.00023332686,0.00017627708,0.00029190167,0.00021457509,0.00017139806,0.00022607711,0.00029675162,0.0004514944],"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":[0.000065152686,0.000010260719,0.0013620204,0.000044218494,0.0000071170784,0.000025679838,0.000024500157,0.00017145307,0.9944326,0.00003939496,0.000045728073,0.0037717465],"study_design_scores_gemma":[0.000025961279,0.0005616049,0.037908316,0.000011979162,0.000041484658,0.0003491955,0.000059124544,0.0032690405,0.9554162,0.000094798095,0.002251884,0.000010405919],"about_ca_topic_score_codex":0.0005590703,"about_ca_topic_score_gemma":0.0012702153,"teacher_disagreement_score":0.00153286,"about_ca_system_score_codex":0.00018053339,"about_ca_system_score_gemma":0.00016730207,"threshold_uncertainty_score":0.005127907},"labels":[],"label_agreement":null},{"id":"W2024941354","doi":"10.1007/s00439-007-0442-z","title":"Parental transmission of HLA-DRB1*15 in multiple sclerosis","year":2007,"lang":"en","type":"article","venue":"Human Genetics","topic":"Genetic Syndromes and Imprinting","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":"University of British Columbia","funders":"Multiple Sclerosis Society","keywords":"Biology; Human genetics; Multiple sclerosis; Human leukocyte antigen; Metabolic disease; Transmission (telecommunications); Genetics; Molecular medicine; Evolutionary biology; Immunology; Antigen; Gene","score_opus":0.03670862111484145,"score_gpt":0.2617135730244857,"score_spread":0.22500495190964426,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2024941354","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9960044,0.00063238584,0.00060082984,0.00011475467,0.00002281045,0.0000032203513,0.00007869992,0.000022945724,0.0025199375],"genre_scores_gemma":[0.9988757,0.00031804983,0.00019811885,0.00001808553,0.000014242698,0.0000029260107,0.000029686824,0.0000068226122,0.0005362768],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9996165,0.00020004637,0.000033813532,0.00005879642,0.000044107644,0.00004672961],"domain_scores_gemma":[0.9991684,0.00040768724,0.00016528025,0.00009757824,0.000030707753,0.00013026143],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0004161794,0.0003381786,0.0002562399,0.0010852866,0.00048018646,0.0002783097,0.00032051883,0.0004743243,0.0050470517],"category_scores_gemma":[0.0016588839,0.00030343156,0.0001891324,0.00069011585,0.00047326295,0.00027053925,0.0005521565,0.00041274182,0.00038659945],"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":[0.008119269,0.00066089665,0.52095765,0.00022218884,0.00051759864,0.12318011,0.004666495,0.0018940343,0.24653727,0.020044442,0.0018211206,0.0713789],"study_design_scores_gemma":[0.00041794663,0.0014925972,0.7532951,0.00014177534,0.0008046668,0.16449597,0.0021164746,0.002566959,0.06077371,0.0076392656,0.006170013,0.00008542278],"about_ca_topic_score_codex":0.0011151853,"about_ca_topic_score_gemma":0.00083178544,"teacher_disagreement_score":0.0050470517,"about_ca_system_score_codex":0.00020669446,"about_ca_system_score_gemma":0.00014561479,"threshold_uncertainty_score":0.016884089},"labels":[],"label_agreement":null},{"id":"W2026012701","doi":"10.1159/000056887","title":"Analysis of DEXI/&lt;i&gt;Dexi&lt;/i&gt; refines the organization of the mouse 7C and human 15q11→q13 imprinting clusters","year":2001,"lang":"en","type":"article","venue":"Cytogenetic and Genome Research","topic":"Genetic Syndromes and Imprinting","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":"University of Alberta","funders":"","keywords":"Biology; Angelman syndrome; Genetics; Gene; Imprinting (psychology); Chromosome; Genomic imprinting; Gene expression","score_opus":0.026756667633003474,"score_gpt":0.296731008099264,"score_spread":0.2699743404662605,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2026012701","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9585682,0.00061132666,0.0316474,0.0002117157,0.000034968172,0.000040655887,0.0030153766,0.00034871246,0.005521633],"genre_scores_gemma":[0.9512781,0.00058219675,0.032941546,0.00015696071,0.000012064743,0.00006762871,0.0065749506,0.00029409907,0.008092585],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99989414,0.000008452917,0.000008154817,0.000047697973,0.000022484926,0.000019088426],"domain_scores_gemma":[0.99979466,0.000042915817,0.000055476055,0.000039067847,0.000018657938,0.000049280527],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00014486002,0.00030119528,0.00026239737,0.0005551894,0.00023042629,0.0002893349,0.00042191945,0.00020072168,0.003928891],"category_scores_gemma":[0.00016907381,0.00019204576,0.00032588726,0.0003657251,0.0004455487,0.00017247122,0.0002896915,0.00054359896,0.001232531],"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":[0.000093266426,0.000010986877,0.0013376793,0.000024181865,0.0000059153435,0.00009309235,0.00002659792,0.00010978608,0.99436355,0.00036884492,0.000059536105,0.0035064502],"study_design_scores_gemma":[0.000023768582,0.000093226445,0.04018549,0.000013026666,0.000037414808,0.000877084,0.000054786182,0.0013977507,0.94225764,0.00041069972,0.014640041,0.000009004757],"about_ca_topic_score_codex":0.001509052,"about_ca_topic_score_gemma":0.0030856745,"teacher_disagreement_score":0.003928891,"about_ca_system_score_codex":0.00042391988,"about_ca_system_score_gemma":0.00021113032,"threshold_uncertainty_score":0.01314348},"labels":[],"label_agreement":null},{"id":"W2026126802","doi":"10.1016/s0925-4773(02)00018-7","title":"Cloning of the mouse Sef gene and comparative analysis of its expression with Fgf8 and Spry2 during embryogenesis","year":2002,"lang":"en","type":"article","venue":"Mechanisms of Development","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":68,"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":"Centre National de la Recherche Scientifique; Institut national de la recherche scientifique","keywords":"FGF8; Biology; Forebrain; Cloning (programming); Hindbrain; Embryo; Embryogenesis; Limb bud; Neuroepithelial cell; Gene; EMX2; Morphogen; Genetics; Fibroblast growth factor; Embryonic stem cell; Cell biology; Gene expression; Anatomy; Homeobox; Neuroscience; Central nervous system","score_opus":0.016155251214197145,"score_gpt":0.2104422705748611,"score_spread":0.19428701936066395,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2026126802","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9777025,0.0033098783,0.015313527,0.00015247575,0.000027916753,0.00004520459,0.00094942574,0.00015089437,0.0023481713],"genre_scores_gemma":[0.96241385,0.0028078011,0.018211829,0.00007547964,0.00002350202,0.00009632695,0.0034922226,0.000111816255,0.012767164],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99991083,0.000007471617,0.000010690672,0.00001847711,0.000021626152,0.000030944077],"domain_scores_gemma":[0.99980944,0.00005074543,0.000042045212,0.000024825065,0.000029387245,0.000043453532],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00016169636,0.0003027023,0.0003175433,0.00077055854,0.00027530378,0.00032413568,0.00041431808,0.00033334838,0.0010478193],"category_scores_gemma":[0.00017832979,0.0003991543,0.0004096721,0.00035241476,0.00033827292,0.0003905145,0.0002650599,0.0005817378,0.00073186844],"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":[0.00011704402,0.00000822824,0.00036065042,0.000019425246,0.0000027261992,0.00011392715,0.00002747766,0.00007440501,0.99691015,0.0004938497,0.000016887923,0.0018551836],"study_design_scores_gemma":[0.000019999345,0.0001044904,0.011631584,0.000012516321,0.000014212624,0.0004977901,0.00004781661,0.00034862699,0.981783,0.00016739515,0.0053665005,0.000006123667],"about_ca_topic_score_codex":0.0013482241,"about_ca_topic_score_gemma":0.0016420565,"teacher_disagreement_score":0.0013482241,"about_ca_system_score_codex":0.00036709034,"about_ca_system_score_gemma":0.00021673864,"threshold_uncertainty_score":0.0035052896},"labels":[],"label_agreement":null},{"id":"W2026274018","doi":"10.1016/j.ydbio.2008.04.025","title":"Altered gene expression and methylation of the human chromosome 11 imprinted region in small for gestational age (SGA) placentae","year":2008,"lang":"en","type":"article","venue":"Developmental Biology","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":163,"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; Hospital for Sick Children; University of Toronto","funders":"Fundação para a Ciência e a Tecnologia; Canadian Institutes of Health Research","keywords":"Genomic imprinting; Biology; Epigenetics; Imprinting (psychology); Placenta; DNA methylation; Methylation; Fetus; Cord blood; Gene; Gene expression; Genetics; Molecular biology; Andrology; Pregnancy","score_opus":0.032253366362057924,"score_gpt":0.2585050768203609,"score_spread":0.22625171045830297,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2026274018","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99830806,0.00064090616,0.00030903507,0.000029135706,0.000006012092,0.0000026666135,0.00020299105,0.000009065072,0.00049204926],"genre_scores_gemma":[0.99850684,0.00033498358,0.0001741159,0.000013175292,0.0000041781623,0.0000046496175,0.00020743455,0.000005759763,0.0007489657],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9999156,0.00001931987,0.000005950959,0.00001961577,0.000018486522,0.000020979402],"domain_scores_gemma":[0.9998184,0.00006177243,0.00004689889,0.000019051751,0.000018297898,0.000035640976],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.000112482565,0.000113698225,0.00019019865,0.00061968336,0.00013965857,0.00026444628,0.00013141318,0.00018968486,0.001096973],"category_scores_gemma":[0.000434032,0.00019255513,0.000119471835,0.0002943116,0.0002771589,0.0000917548,0.00017768261,0.00022548964,0.00017400128],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0016041426,0.000026810912,0.04030372,0.000052959047,0.00004272311,0.0007739477,0.0004288188,0.00011854501,0.95129687,0.00023626986,0.0000953471,0.005019889],"study_design_scores_gemma":[0.000029860486,0.00028356683,0.84961504,0.000009760162,0.0000628125,0.0035752303,0.00049246626,0.0005068528,0.14341351,0.0003563077,0.0016411535,0.000013416145],"about_ca_topic_score_codex":0.0017721739,"about_ca_topic_score_gemma":0.0011776042,"teacher_disagreement_score":0.0017721739,"about_ca_system_score_codex":0.00016190464,"about_ca_system_score_gemma":0.00012818273,"threshold_uncertainty_score":0.0036697388},"labels":[],"label_agreement":null},{"id":"W2027258743","doi":"10.1007/s10735-011-9337-3","title":"Imprinting and expression analysis of a non-coding RNA gene in the mouse Dlk1-Dio3 domain","year":2011,"lang":"en","type":"article","venue":"Journal of Molecular Histology","topic":"Genetic Syndromes and Imprinting","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":"Princess Margaret Cancer Centre","funders":"RIKEN; National Natural Science Foundation of China; Heilongjiang Youth Development Foundation","keywords":"Genomic imprinting; Imprinting (psychology); Gene; Gene expression; RNA; Developmental biology; Biology; Genetics; Coding (social sciences); Computational biology; Molecular biology; Mathematics; DNA methylation; Statistics","score_opus":0.011018480282029624,"score_gpt":0.23399685307248191,"score_spread":0.2229783727904523,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2027258743","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99031466,0.00076781906,0.0048629832,0.00013123376,0.000024610097,0.00001972373,0.0012623157,0.00011971395,0.0024969834],"genre_scores_gemma":[0.98838437,0.00032210271,0.0028087026,0.00008201959,0.000006155595,0.00002436908,0.0015190415,0.00015294092,0.0067003057],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99981815,0.000010692894,0.000014575698,0.00006340216,0.00004428211,0.000048950053],"domain_scores_gemma":[0.99967957,0.00007298663,0.00010510194,0.000038000475,0.000021772383,0.00008249019],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00011571294,0.00027920667,0.00017427377,0.0006073175,0.00024911895,0.00034294263,0.00036379552,0.0003882243,0.0019900163],"category_scores_gemma":[0.00015219694,0.0003134377,0.0003541646,0.00024957853,0.00044338495,0.0002363169,0.00027195542,0.00073030253,0.00091332354],"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":[0.000043906835,0.0000046286905,0.00016338295,0.000007902382,0.0000017446362,0.000057452224,0.000007561043,0.00002359472,0.999308,0.00012154797,0.000009388787,0.00025075965],"study_design_scores_gemma":[0.000019014271,0.00004343702,0.013201373,0.000004693216,0.000020607325,0.00048108568,0.000037561687,0.00056411803,0.98399204,0.00010441357,0.0015256054,0.0000059710214],"about_ca_topic_score_codex":0.0014933421,"about_ca_topic_score_gemma":0.0034766165,"teacher_disagreement_score":0.0019900163,"about_ca_system_score_codex":0.00051110977,"about_ca_system_score_gemma":0.00022222854,"threshold_uncertainty_score":0.0066573024},"labels":[],"label_agreement":null},{"id":"W2027302112","doi":"10.1053/plac.2002.0892","title":"‘Imprinting and Growth Congress’ 2002, London, UK","year":2002,"lang":"en","type":"article","venue":"Placenta","topic":"Genetic Syndromes and Imprinting","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":"University of Calgary","funders":"","keywords":"Imprinting (psychology); Biology; Genetics","score_opus":0.011164740113076346,"score_gpt":0.21433378095238323,"score_spread":0.20316904083930687,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2027302112","genre_codex":"review","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":[0.0039474405,0.6265061,0.0022486735,0.061555844,0.05251601,0.000103571045,0.0021524564,0.00049654156,0.25047338],"genre_scores_gemma":[0.016146585,0.21025309,0.0013001767,0.0042273863,0.0077480515,0.00016598972,0.00095322245,0.00020430796,0.75900114],"study_design_codex":"not_applicable","study_design_gemma":"not_applicable","domain_scores_codex":[0.99941015,0.000085974934,0.00007112905,0.00013397147,0.00019957579,0.000099243094],"domain_scores_gemma":[0.9993424,0.0001767877,0.00008766971,0.000046410347,0.00014929357,0.00019745411],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00077391026,0.0016162598,0.0011869649,0.0012937888,0.0010303245,0.0033991896,0.0011723165,0.0037517138,0.17743888],"category_scores_gemma":[0.0010859041,0.0006049033,0.0005586668,0.001979615,0.0012720563,0.0027571057,0.002089662,0.0033165938,0.06663707],"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":[0.00033097662,0.000020375473,0.00022055577,0.0009804895,0.000028387725,0.00075706554,0.00015822171,0.00042319964,0.0022950515,0.007973594,0.71169305,0.275119],"study_design_scores_gemma":[0.000014725714,0.000020636386,0.0008365045,0.00029978712,0.000007220822,0.0002532232,0.00008520441,0.000036156,0.0001901141,0.00047659792,0.99777216,0.0000075880826],"about_ca_topic_score_codex":0.0046397443,"about_ca_topic_score_gemma":0.015480657,"teacher_disagreement_score":0.17743888,"about_ca_system_score_codex":0.002199072,"about_ca_system_score_gemma":0.001032901,"threshold_uncertainty_score":0.59359217},"labels":[],"label_agreement":null},{"id":"W2027976282","doi":"10.1016/j.ygeno.2011.10.007","title":"Maternal gametic transmission of translocations or inversions of human chromosome 11p15.5 results in regional DNA hypermethylation and downregulation of CDKN1C expression","year":2011,"lang":"en","type":"article","venue":"Genomics","topic":"Genetic Syndromes and Imprinting","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":"Kingston General Hospital; Queen's University; Hospital for Sick Children; BC Cancer Agency","funders":"National Institute of General Medical Sciences","keywords":"Biology; Genomic imprinting; DNA methylation; Chromosomal translocation; Genetics; Epigenetics; Chromosome; Gene; Gene expression","score_opus":0.033697568164484826,"score_gpt":0.24765140357620719,"score_spread":0.21395383541172236,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2027976282","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99339443,0.0007380463,0.0030274228,0.0000893358,0.000030786425,0.000012547689,0.00048360202,0.000065186294,0.0021586572],"genre_scores_gemma":[0.99738604,0.00035153847,0.00036449576,0.000019088162,0.0000038692915,0.000008249026,0.00025014236,0.000011883663,0.0016046832],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9998807,0.000022253951,0.00000850904,0.000036663976,0.0000318031,0.000020151185],"domain_scores_gemma":[0.999899,0.000027024636,0.000032559004,0.000013710383,0.0000045844126,0.000023095852],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0001289455,0.00028527033,0.00015634524,0.00032679076,0.00010109117,0.00019429115,0.0001723683,0.00016889286,0.0033688964],"category_scores_gemma":[0.0002418839,0.00017758166,0.00013126765,0.00016427237,0.0003189748,0.00007734396,0.00024971846,0.00026737954,0.00037461772],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00028956158,0.0000300344,0.0056131883,0.00004133596,0.000033773576,0.0016980016,0.00006106275,0.00011513143,0.9863637,0.0006596248,0.00022034503,0.004874188],"study_design_scores_gemma":[0.000090895046,0.0003306838,0.1702159,0.00001790854,0.00012799152,0.011735097,0.00017451574,0.000658694,0.81066096,0.0004777057,0.005496105,0.000013482979],"about_ca_topic_score_codex":0.0013337681,"about_ca_topic_score_gemma":0.002778399,"teacher_disagreement_score":0.0033688964,"about_ca_system_score_codex":0.000191802,"about_ca_system_score_gemma":0.00022603403,"threshold_uncertainty_score":0.011270046},"labels":[],"label_agreement":null},{"id":"W2028231466","doi":"10.1016/j.jpeds.2006.08.077","title":"Normal minipuberty of infancy in boys with Prader-Willi syndrome","year":2006,"lang":"en","type":"article","venue":"The Journal of Pediatrics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":39,"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":"","keywords":"Medicine; Endocrinology; Testosterone (patch); Internal medicine; Degeneration (medical); Hormone; Gonadotropin; Pathology","score_opus":0.004796305795310028,"score_gpt":0.20431633553648984,"score_spread":0.1995200297411798,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2028231466","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9946327,0.001095869,0.00060080655,0.00012219822,0.00004895013,0.00001607503,0.00017332693,0.00013805035,0.0031720214],"genre_scores_gemma":[0.9977435,0.00058044674,0.00043521906,0.000035706664,0.000047187354,0.000012456534,0.0001020374,0.00004170302,0.0010017204],"study_design_codex":"case_report","study_design_gemma":"observational","domain_scores_codex":[0.99956113,0.0000719291,0.00003888964,0.00007730426,0.00016151069,0.00008928769],"domain_scores_gemma":[0.99885786,0.00045260348,0.00024973333,0.00008342347,0.00011906076,0.00023739648],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00029370867,0.0006399461,0.0009877698,0.002060993,0.00046137863,0.0004817181,0.00075049384,0.00071846886,0.0015750696],"category_scores_gemma":[0.003515011,0.00050645246,0.00029843807,0.0004503948,0.0009933145,0.00045229518,0.00071147643,0.00077824766,0.0003193497],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0039353403,0.00043116685,0.21958935,0.00036525403,0.00012112299,0.45531294,0.0039664344,0.0010568218,0.26638594,0.0022718655,0.0012179094,0.045345865],"study_design_scores_gemma":[0.00005677223,0.0017515696,0.48849806,0.000054760436,0.00015389275,0.42966452,0.0008016494,0.0012589982,0.073032655,0.00061539817,0.004051927,0.0000597026],"about_ca_topic_score_codex":0.0015735691,"about_ca_topic_score_gemma":0.0008395371,"teacher_disagreement_score":0.002060993,"about_ca_system_score_codex":0.00030313607,"about_ca_system_score_gemma":0.00036005417,"threshold_uncertainty_score":0.00526917},"labels":[],"label_agreement":null},{"id":"W2028337288","doi":"10.1002/1096-8628(20001113)95:2<182::aid-ajmg18>3.0.co;2-8","title":"Sacrococcygeal teratoma in two cases of Sotos syndrome","year":2000,"lang":"en","type":"letter","venue":"American Journal of Medical Genetics","topic":"Genetic Syndromes and Imprinting","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":"Glenrose Rehabilitation Hospital; University of Alberta; Alberta Hospital Edmonton; University of Alberta Hospital","funders":"","keywords":"Sotos syndrome; Medicine; Pediatrics","score_opus":0.008802131237567724,"score_gpt":0.28080934008242137,"score_spread":0.27200720884485363,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2028337288","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.98137695,0.0012815817,0.0014788862,0.003763166,0.0005756573,0.00016514247,0.0002881375,0.00019927073,0.010871205],"genre_scores_gemma":[0.9958358,0.00031249368,0.0011524842,0.0005765216,0.0006760734,0.000036379544,0.0000853263,0.00003539415,0.0012896333],"study_design_codex":"case_report","study_design_gemma":"case_report","domain_scores_codex":[0.99897754,0.00013930073,0.00011720546,0.00021620694,0.00020140233,0.00034838018],"domain_scores_gemma":[0.9948731,0.0020638246,0.0010275511,0.00051213894,0.00020451074,0.0013189205],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0007477475,0.001945679,0.001588867,0.002969383,0.0021218837,0.0017630812,0.0018862088,0.0076301876,0.0025714906],"category_scores_gemma":[0.008864294,0.0013217365,0.0013430568,0.0015874888,0.003244947,0.0014218064,0.0020734465,0.0029379479,0.0006248498],"study_design_candidate":"case_report","study_design_consensus":"case_report","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00010009048,0.000020444479,0.0037788851,0.000016100248,0.0000069931116,0.99429107,0.0001239113,0.00006994709,0.0005393206,0.000328298,0.00016501076,0.0005598858],"study_design_scores_gemma":[0.000112466914,0.00011783071,0.008555791,0.000008500591,0.000026072184,0.9886742,0.00013647006,0.0005172817,0.00082311203,0.00042697665,0.0005829698,0.00001822541],"about_ca_topic_score_codex":0.002919902,"about_ca_topic_score_gemma":0.0024363014,"teacher_disagreement_score":0.0076301876,"about_ca_system_score_codex":0.001937342,"about_ca_system_score_gemma":0.00078718195,"threshold_uncertainty_score":0},"labels":[],"label_agreement":null},{"id":"W2028882980","doi":"10.1007/s10024001-0110-6","title":"Association of Alveolar Rhabdomyosarcoma with the Beckwith-Wiedemann Syndrome","year":2001,"lang":"en","type":"article","venue":"Pediatric and Developmental Pathology","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":61,"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; Hospital for Sick Children; Canada Research Chairs; University of Toronto","funders":"","keywords":"Beckwith–Wiedemann syndrome; Alveolar rhabdomyosarcoma; Hepatoblastoma; Medicine; Rhabdomyosarcoma; Pathology; Wilms' tumor; Neuroblastoma; PAX3; Embryonal rhabdomyosarcoma; Sarcoma; Internal medicine; Biology","score_opus":0.004815583387863834,"score_gpt":0.1945053870438261,"score_spread":0.18968980365596227,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2028882980","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99446094,0.0012762955,0.0018529684,0.00010485604,0.00003075025,0.000019377927,0.00007642252,0.000072880255,0.0021055394],"genre_scores_gemma":[0.9978066,0.00042148266,0.0012419975,0.00006357619,0.000040727427,0.0000082771585,0.00007709053,0.00000943724,0.00033076247],"study_design_codex":"case_report","study_design_gemma":"case_report","domain_scores_codex":[0.9997578,0.000032909422,0.000044994926,0.000051305316,0.000049286227,0.0000636228],"domain_scores_gemma":[0.99923027,0.00022202297,0.0003131393,0.00006512813,0.000045780904,0.00012366999],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00020362121,0.00046590224,0.00028001016,0.0007392562,0.00047555982,0.0003738687,0.00025824932,0.0005149784,0.00080632756],"category_scores_gemma":[0.0011224498,0.000360816,0.00041475517,0.00053258194,0.00077885564,0.0003546241,0.0006184861,0.00050872716,0.0002351959],"study_design_candidate":"case_report","study_design_consensus":"case_report","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00011654809,0.00004159869,0.30656746,0.000113409376,0.000086946275,0.6530304,0.0005983942,0.00032994023,0.021906514,0.00081934873,0.0007034888,0.015685968],"study_design_scores_gemma":[0.000012008225,0.00011301558,0.08691862,0.0000189217,0.000042841337,0.90783393,0.00017365292,0.00022218218,0.002554889,0.00016987503,0.0019238371,0.000016282384],"about_ca_topic_score_codex":0.001155537,"about_ca_topic_score_gemma":0.0032304693,"teacher_disagreement_score":0.001155537,"about_ca_system_score_codex":0.00022476372,"about_ca_system_score_gemma":0.0003014561,"threshold_uncertainty_score":0.0026974678},"labels":[],"label_agreement":null},{"id":"W2029294068","doi":"10.1007/s00438-002-0731-0","title":"Genomic imprinting in Drosophila is maintained by the products of Suppressor of variegation and trithorax group, but not Polycomb group, genes","year":2002,"lang":"en","type":"article","venue":"Molecular Genetics and Genomics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","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":"Dalhousie University","funders":"","keywords":"Biology; Polycomb-group proteins; Genetics; Gene; Suppressor; Genomic imprinting; Variegation (histology); Gene expression; DNA methylation; Repressor","score_opus":0.008347261510660066,"score_gpt":0.2033848917433187,"score_spread":0.19503763023265863,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2029294068","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9940499,0.0011706776,0.0024259042,0.00006445098,0.00002179944,0.0000037189993,0.0002797181,0.0001512242,0.0018326587],"genre_scores_gemma":[0.9958358,0.00040625807,0.0010134769,0.000024230303,0.0000079589345,0.0000045368324,0.0004794266,0.0000414173,0.0021869503],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9999244,0.0000074473605,0.000005102437,0.000020335665,0.000027802638,0.000014946595],"domain_scores_gemma":[0.9998306,0.000023787175,0.000071598995,0.000020378757,0.000012115885,0.000041456657],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00007060062,0.00032700266,0.00013318485,0.0004258296,0.00017337626,0.00027547762,0.00021395384,0.0001498354,0.00082602113],"category_scores_gemma":[0.00014657671,0.00017721765,0.00013099295,0.00019567487,0.00030955896,0.00020448487,0.0002539977,0.00031483872,0.00035554334],"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":[0.000086817614,0.0000033230162,0.0005790689,0.000010682399,0.0000047454287,0.00009678473,0.000011896413,0.000033594515,0.9976318,0.00027940818,0.000033714845,0.0012280444],"study_design_scores_gemma":[0.00003101107,0.00011627606,0.041676965,0.000005410158,0.000040988252,0.0012577435,0.000044746997,0.0009463979,0.9522197,0.00044500173,0.0032077627,0.000007959906],"about_ca_topic_score_codex":0.0009330204,"about_ca_topic_score_gemma":0.0027055603,"teacher_disagreement_score":0.0009330204,"about_ca_system_score_codex":0.00027791646,"about_ca_system_score_gemma":0.00015501621,"threshold_uncertainty_score":0.002763331},"labels":[],"label_agreement":null},{"id":"W2029736005","doi":"10.1007/s00335-001-2095-x","title":"Inheritance patterns of maternal alleles in imprinted regions of the mouse genome at different stages of development","year":2002,"lang":"en","type":"article","venue":"Mammalian Genome","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","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; Royal Victoria Hospital","funders":"Canadian Institutes of Health Research","keywords":"Genomic imprinting; Biology; Allele; Genetics; Offspring; Imprinting (psychology); Mendelian inheritance; Genome; Embryo; Non-Mendelian inheritance; Gene; Meiotic drive; Pregnancy","score_opus":0.014799566627643063,"score_gpt":0.20804145210537517,"score_spread":0.1932418854777321,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2029736005","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99556607,0.00090275134,0.0014092575,0.00004638991,0.000007054083,0.0000043354094,0.0005202526,0.000087540146,0.001456273],"genre_scores_gemma":[0.99578863,0.00045440783,0.00100118,0.000027287022,0.000007193812,0.000009651655,0.00042126776,0.00004547449,0.0022449216],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9997844,0.000028332242,0.000021864707,0.000057908946,0.000056191915,0.000051445146],"domain_scores_gemma":[0.9992768,0.00017590112,0.00027599622,0.00006290085,0.00007738679,0.00013096454],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00020112628,0.00024037457,0.00024333375,0.0016552623,0.00020499458,0.00041459387,0.0003037349,0.00030344777,0.0014585187],"category_scores_gemma":[0.0004607181,0.00034568977,0.00020291303,0.0004675934,0.0004299718,0.00021743578,0.00035075966,0.0005168003,0.00039003644],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0003932448,0.000014682541,0.007883947,0.00003021259,0.000021792754,0.00015502644,0.00007291891,0.00009409349,0.98754275,0.00037627816,0.000040774845,0.0033744092],"study_design_scores_gemma":[0.000055379653,0.00021294015,0.3784189,0.00002171687,0.00015596056,0.0020028788,0.00016927744,0.0009100557,0.616001,0.0007032455,0.0013154906,0.000033162876],"about_ca_topic_score_codex":0.0009383891,"about_ca_topic_score_gemma":0.0014025725,"teacher_disagreement_score":0.0016552623,"about_ca_system_score_codex":0.000282785,"about_ca_system_score_gemma":0.0001371778,"threshold_uncertainty_score":0.004879236},"labels":[],"label_agreement":null},{"id":"W2031586320","doi":"10.1006/geno.2002.6732","title":"Methylation Dynamics of Imprinted Genes in Mouse Germ Cells","year":2002,"lang":"en","type":"article","venue":"Genomics","topic":"Genetic Syndromes and Imprinting","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":"McGill University; Royal Victoria Hospital; Montreal Children's Hospital","funders":"","keywords":"Biology; Genomic imprinting; Methylation; DNA methylation; Genetics; Differentially methylated regions; Bisulfite sequencing; Gene; Gene expression","score_opus":0.01045759288624632,"score_gpt":0.21502962807787065,"score_spread":0.20457203519162434,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2031586320","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9913878,0.0017423711,0.0045493864,0.00007068538,0.0000112938815,0.0000031452282,0.000291355,0.000101087346,0.0018427845],"genre_scores_gemma":[0.99673235,0.00046398368,0.000894033,0.000016125225,0.000005242743,0.000005126568,0.00020256611,0.000022002578,0.0016586456],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9999393,0.0000076005836,0.0000029934342,0.000016876402,0.000019372563,0.00001373292],"domain_scores_gemma":[0.9999099,0.000015972562,0.000025832955,0.000011027075,0.000016601503,0.0000206599],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.000100519326,0.00010546497,0.00012434185,0.00037905504,0.00014494556,0.0003543485,0.0001931069,0.00015422037,0.00064030755],"category_scores_gemma":[0.00017269485,0.00018560655,0.00008389358,0.00020178956,0.00019031457,0.00025680166,0.00013520455,0.00025900657,0.00022426622],"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":[0.00011203234,0.0000032346572,0.0014276648,0.000011576751,0.000004460703,0.00002351528,0.00004190265,0.00016433535,0.9950653,0.00085717125,0.000038728347,0.0022501182],"study_design_scores_gemma":[0.000012139493,0.00007661391,0.050539568,0.0000048933566,0.000017867638,0.0002164042,0.00007131619,0.0022816886,0.9428997,0.00092320575,0.0029471104,0.000009489557],"about_ca_topic_score_codex":0.0013925491,"about_ca_topic_score_gemma":0.001585694,"teacher_disagreement_score":0.0013925491,"about_ca_system_score_codex":0.0003065457,"about_ca_system_score_gemma":0.000120362136,"threshold_uncertainty_score":0.0027688742},"labels":[],"label_agreement":null},{"id":"W2031791275","doi":"10.1006/geno.2000.6155","title":"Alterations of H19 Imprinting and IGF2 Replication Timing Are Infrequent in Beckwith–Wiedemann Syndrome","year":2000,"lang":"en","type":"article","venue":"Genomics","topic":"Genetic Syndromes and Imprinting","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":"SickKids Foundation; Hospital for Sick Children; University of Toronto; Ontario Institute for Cancer Research","funders":"National Cancer Institute","keywords":"Imprinting (psychology); Genomic imprinting; Biology; Beckwith–Wiedemann syndrome; DNA methylation; Replication timing; Genetics; Methylation; Insulin-like growth factor 2; Gene; DNA replication; Gene expression","score_opus":0.013001737606654226,"score_gpt":0.24067449648459494,"score_spread":0.2276727588779407,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2031791275","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9954431,0.0011454697,0.0008483249,0.00010583205,0.000031193566,0.000006504841,0.00043734084,0.000066384324,0.0019158362],"genre_scores_gemma":[0.9985672,0.00031635974,0.00060448085,0.000026815516,0.000022443826,0.000005071828,0.0002007655,0.000017125552,0.00023965848],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9995789,0.000077075005,0.0000614771,0.00009644627,0.00009601567,0.00009005259],"domain_scores_gemma":[0.9988751,0.0005023492,0.00032236727,0.00007731179,0.00007064316,0.00015234393],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00020139993,0.00064648385,0.0004568597,0.002420307,0.00033224805,0.00036908104,0.0003575016,0.0007395011,0.0034234687],"category_scores_gemma":[0.002260944,0.00029770035,0.00021188192,0.0009572935,0.0005330647,0.000347398,0.00031859643,0.0002824326,0.00039326467],"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":[0.0023320597,0.000112685186,0.6096741,0.00022523425,0.00022630372,0.07310937,0.0006559972,0.00060011685,0.2672008,0.0011466715,0.0011470702,0.04356959],"study_design_scores_gemma":[0.000050335253,0.00033810755,0.8092171,0.000048643462,0.00024472942,0.13286701,0.0004305201,0.00069765316,0.050937224,0.0010173282,0.0040999167,0.000051388615],"about_ca_topic_score_codex":0.0014277386,"about_ca_topic_score_gemma":0.0012674853,"teacher_disagreement_score":0.0034234687,"about_ca_system_score_codex":0.00013835735,"about_ca_system_score_gemma":0.00020883151,"threshold_uncertainty_score":0.011452675},"labels":[],"label_agreement":null},{"id":"W2032030931","doi":"10.1002/ajmg.a.32669","title":"A patient with the Simpson–Golabi–Behmel syndrome displays a loss‐of‐function point mutation in <i>GPC3</i> that inhibits the attachment of this proteoglycan to the cell surface","year":2009,"lang":"en","type":"article","venue":"American Journal of Medical Genetics Part A","topic":"Genetic Syndromes and Imprinting","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":"Health Sciences Centre; University of Toronto; Sunnybrook Health Science Centre","funders":"","keywords":"Medicine; Chemistry","score_opus":0.005504491112100869,"score_gpt":0.23195294459630225,"score_spread":0.2264484534842014,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2032030931","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9904454,0.00040548382,0.0013804507,0.0019872973,0.0001657975,0.000041800253,0.00024047111,0.00010260403,0.005230775],"genre_scores_gemma":[0.997632,0.00013015159,0.00066750124,0.00035510905,0.000102739155,0.000005658954,0.00006511654,0.000019459269,0.0010221675],"study_design_codex":"case_report","study_design_gemma":"case_report","domain_scores_codex":[0.99973875,0.000028787854,0.000030352729,0.00006956593,0.00006234119,0.000070179645],"domain_scores_gemma":[0.99907446,0.00041133343,0.00010181809,0.000039902206,0.000049597,0.0003229517],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00022353164,0.0018189178,0.00071764155,0.0011131454,0.0013616619,0.00069168984,0.00054285745,0.0026755726,0.0018086918],"category_scores_gemma":[0.0017922821,0.00054048945,0.00053360104,0.0007039644,0.0013325866,0.00045563353,0.00064890925,0.0013082512,0.00050402957],"study_design_candidate":"case_report","study_design_consensus":"case_report","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0001806837,0.00008037841,0.014224085,0.000029847646,0.000029983277,0.9644005,0.0007844008,0.00020275448,0.015320088,0.0005904162,0.00059289776,0.0035638774],"study_design_scores_gemma":[0.0000421631,0.00019334453,0.017052364,0.0000070743467,0.00003365969,0.97720784,0.00020018022,0.00046219997,0.0033249164,0.0003985838,0.0010509805,0.000026776075],"about_ca_topic_score_codex":0.0041969297,"about_ca_topic_score_gemma":0.0027918413,"teacher_disagreement_score":0.0041969297,"about_ca_system_score_codex":0.00050540885,"about_ca_system_score_gemma":0.00057177385,"threshold_uncertainty_score":0.008345008},"labels":[],"label_agreement":null},{"id":"W2032393199","doi":"10.1091/mbc.e06-10-0920","title":"Bsr, a Nuclear-retained RNA with Monoallelic Expression","year":2007,"lang":"en","type":"article","venue":"Molecular Biology of the Cell","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":28,"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 Sherbrooke","funders":"European Commission","keywords":"Biology; Non-coding RNA; Intron; RNA; Transcription (linguistics); Small nucleolar RNA; Gene; Gene expression; Molecular biology; Genetics; RNA splicing; Mature messenger RNA; Cell biology","score_opus":0.004162566628859801,"score_gpt":0.21397114972129436,"score_spread":0.20980858309243455,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2032393199","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9787073,0.0030809562,0.013872293,0.00007882738,0.000033296546,0.00003067802,0.00075962034,0.00034486418,0.0030921786],"genre_scores_gemma":[0.9890588,0.00095931854,0.0049885423,0.000023148641,0.000012727402,0.000019984229,0.0009174069,0.00004459533,0.003975483],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9999094,0.000013763412,0.0000057049742,0.000039366012,0.000020962234,0.0000107632595],"domain_scores_gemma":[0.9999192,0.000018301418,0.00002909464,0.000010717711,0.0000054527873,0.000017191067],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.000074938565,0.0004182507,0.00010502439,0.0002340595,0.00008823853,0.0001567393,0.00018331484,0.00018074541,0.0010532476],"category_scores_gemma":[0.00008033637,0.00009503381,0.00009740385,0.00010842318,0.00025510177,0.00009984174,0.00014121368,0.00015404416,0.00045793253],"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":[0.000023863211,0.000002357106,0.0002235436,0.000017149989,0.0000023600662,0.00017829571,0.0000056656204,0.000016289348,0.99835217,0.000110075714,0.000013048443,0.001055097],"study_design_scores_gemma":[0.000008693619,0.00013401534,0.013255821,0.000005189351,0.000017540102,0.0032277699,0.000033066197,0.00051932473,0.97734433,0.00011598935,0.0053329663,0.000005154691],"about_ca_topic_score_codex":0.0003104317,"about_ca_topic_score_gemma":0.0005566544,"teacher_disagreement_score":0.0010532476,"about_ca_system_score_codex":0.00019219745,"about_ca_system_score_gemma":0.000113077054,"threshold_uncertainty_score":0.003523469},"labels":[],"label_agreement":null},{"id":"W2032664909","doi":"10.1016/j.placenta.2008.02.013","title":"Morphological and Electrical Properties of Human Trophoblast Choriocarcinoma, BeWo Cells","year":2008,"lang":"en","type":"article","venue":"Placenta","topic":"Genetic Syndromes and Imprinting","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":"Memorial University of Newfoundland","funders":"PKD Foundation","keywords":"Syncytium; Syncytiotrophoblast; Cytotrophoblast; Cell biology; Cell fusion; Intracellular; Biology; Trophoblast; Cell type; Multinucleate; Cell culture; Cell; Chemistry; Placenta; Biochemistry","score_opus":0.020723166809227398,"score_gpt":0.21537077266496624,"score_spread":0.19464760585573884,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2032664909","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9929974,0.0010023232,0.0013042189,0.00010718097,0.000019431402,0.000011829208,0.00050434424,0.000017510016,0.004035755],"genre_scores_gemma":[0.99581796,0.00056083675,0.00048768395,0.00003186056,0.0000070552496,0.000015785363,0.0005855895,0.0000090309295,0.0024842748],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9999131,0.000018740726,0.0000097343145,0.000012761479,0.000029452105,0.000016171314],"domain_scores_gemma":[0.999856,0.00005127768,0.00001951785,0.000023239618,0.000027063166,0.000022881022],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00010103085,0.00010682449,0.00010431872,0.00027302836,0.00021849482,0.00033612535,0.000089734596,0.00019848582,0.0009980196],"category_scores_gemma":[0.00031611184,0.0001086341,0.000116652525,0.00039190747,0.0001928515,0.00026552,0.00013500242,0.00022219657,0.00023569516],"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":[0.000217333,0.000012872938,0.0018230758,0.000040330324,0.000007778608,0.00037987286,0.00026884972,0.0000988379,0.9951722,0.00046203876,0.000051568513,0.0014651705],"study_design_scores_gemma":[0.000043500197,0.0003980123,0.18187389,0.000017681516,0.000066235065,0.0039417297,0.0012577607,0.001407806,0.79887897,0.0006887045,0.011399243,0.000026466787],"about_ca_topic_score_codex":0.0016999616,"about_ca_topic_score_gemma":0.0009413066,"teacher_disagreement_score":0.0016999616,"about_ca_system_score_codex":0.00017156746,"about_ca_system_score_gemma":0.00011334922,"threshold_uncertainty_score":0.0033801794},"labels":[],"label_agreement":null},{"id":"W2033993581","doi":"10.1002/ajmg.1549","title":"Evidence for linkage disequilibrium between the alpha 7‐nicotinic receptor gene (CHRNA7) locus and schizophrenia in Azorean families*","year":2001,"lang":"en","type":"article","venue":"American Journal of Medical Genetics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","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 Toronto; Centre for Addiction and Mental Health","funders":"Medical Research Council; Medical Research Council Canada; National Institute of Mental Health; National Alliance for Research on Schizophrenia and Depression","keywords":"Biology; Genetics; Linkage disequilibrium; Transmission disequilibrium test; Exon; Locus (genetics); Genetic association; Candidate gene; Allele; Haplotype; Gene; Single-nucleotide polymorphism; Genotype","score_opus":0.027603197175483804,"score_gpt":0.3084062842291854,"score_spread":0.2808030870537016,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2033993581","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99924004,0.00018073924,0.00010225732,0.000023824101,0.0000021277913,0.0000027325943,0.000042434982,0.000003643301,0.00040215848],"genre_scores_gemma":[0.9990239,0.00017244651,0.00028767122,0.000023149125,0.0000061029127,0.000006789047,0.00011931176,0.0000023389443,0.000358319],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9994073,0.00016139452,0.000046659097,0.00018022985,0.00011049996,0.00009399329],"domain_scores_gemma":[0.99917406,0.00023610296,0.0003028845,0.000057520723,0.00007591983,0.00015347742],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00058713794,0.0003926131,0.00042430058,0.0019907847,0.0010243449,0.00037558627,0.00033541102,0.00031621734,0.0032230113],"category_scores_gemma":[0.001398611,0.00021607052,0.00022697734,0.0010057838,0.00064704294,0.00017093326,0.00053690857,0.00023446108,0.00019558797],"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":[0.0007897658,0.00010224731,0.94413465,0.00005123662,0.00034217985,0.0041110935,0.0016876559,0.0001335753,0.036289588,0.00050274807,0.00019051625,0.011664705],"study_design_scores_gemma":[0.000025810721,0.00016480176,0.9949987,0.00001985739,0.00008797226,0.0030694797,0.00022129556,0.00017892389,0.0005063347,0.00012514472,0.0005911596,0.000010537836],"about_ca_topic_score_codex":0.008892023,"about_ca_topic_score_gemma":0.014098235,"teacher_disagreement_score":0.008892023,"about_ca_system_score_codex":0.0005254361,"about_ca_system_score_gemma":0.00037289108,"threshold_uncertainty_score":0.017680526},"labels":[],"label_agreement":null},{"id":"W2034236394","doi":"10.1182/blood-2010-12-325431","title":"May-Hegglin anomaly","year":2012,"lang":"en","type":"article","venue":"Blood","topic":"Genetic Syndromes and Imprinting","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":"London Health Sciences Centre","funders":"","keywords":"Medicine; Anomaly (physics); Dermatology; Gynecology","score_opus":0.009888508255464501,"score_gpt":0.23192826110470452,"score_spread":0.22203975284924002,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2034236394","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.97583526,0.0035543723,0.0015875563,0.0030730593,0.00025242293,0.00008986556,0.00051528175,0.00024486703,0.014847254],"genre_scores_gemma":[0.9946531,0.0007233204,0.000556885,0.00038884045,0.00014571536,0.00001081899,0.00008209531,0.00001569176,0.0034235537],"study_design_codex":"case_report","study_design_gemma":"case_report","domain_scores_codex":[0.9998281,0.000017309521,0.000012659848,0.00004998117,0.000030173664,0.000061772684],"domain_scores_gemma":[0.9995715,0.00012732828,0.00006604344,0.00002038708,0.000027781589,0.00018696082],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00014122298,0.0010112359,0.0004923869,0.002413982,0.0010873155,0.0005465869,0.0005164342,0.0015196385,0.0040922984],"category_scores_gemma":[0.0013891476,0.0003420121,0.00037733492,0.00083049835,0.0007327659,0.0006704231,0.00056143996,0.0008094003,0.00057394203],"study_design_candidate":"case_report","study_design_consensus":"case_report","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00009248807,0.000045070574,0.014499429,0.000024646826,0.000014503638,0.9782543,0.0001645558,0.00011016789,0.0031437639,0.0006721836,0.00066324935,0.0023155673],"study_design_scores_gemma":[0.000015958718,0.0001171916,0.022074817,0.0000112905545,0.000030712108,0.9731662,0.000130624,0.00025884184,0.0015320786,0.0005329419,0.0021103825,0.000018980387],"about_ca_topic_score_codex":0.0029109186,"about_ca_topic_score_gemma":0.0024546247,"teacher_disagreement_score":0.0040922984,"about_ca_system_score_codex":0.00049537915,"about_ca_system_score_gemma":0.00053321815,"threshold_uncertainty_score":0.013690114},"labels":[],"label_agreement":null},{"id":"W203558109","doi":"10.69645/gwdb6005","title":"Imprinting disorders associated with molecular changes on chromosome 11p15","year":2014,"lang":"en","type":"article","venue":"˜The œbiomedical & life sciences collection.","topic":"Genetic Syndromes and Imprinting","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":"University of Toronto","funders":"","keywords":"Imprinting (psychology); Genomic imprinting; Chromosome; Biology; Genetics; Gene; DNA methylation","score_opus":0.00827545662295314,"score_gpt":0.23322259708629792,"score_spread":0.22494714046334477,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W203558109","genre_codex":"other","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":[0.12555738,0.027804416,0.013879279,0.015704105,0.012735455,0.00079154514,0.016966812,0.0059675453,0.78059345],"genre_scores_gemma":[0.16342798,0.026040368,0.010320995,0.002101563,0.004798612,0.00019420548,0.012924606,0.0005377995,0.7796539],"study_design_codex":"not_applicable","study_design_gemma":"observational","domain_scores_codex":[0.999944,0.0000064392157,0.0000031577217,0.0000080114405,0.000025561076,0.000012914707],"domain_scores_gemma":[0.9998623,0.000045932047,0.00001460378,0.0000048656084,0.0000106605985,0.00006155097],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00012193519,0.0004982589,0.00022587739,0.00088232005,0.00014320387,0.0002906315,0.00020436733,0.0002130626,0.23535356],"category_scores_gemma":[0.00045455937,0.00010055777,0.00013577625,0.0003388066,0.00008105563,0.00020616029,0.00044646687,0.00031915613,0.026770463],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00042262685,0.00007050562,0.00387328,0.00035735467,0.000016428816,0.0033846751,0.00008686477,0.00016369646,0.023795296,0.0016602379,0.6630217,0.30314738],"study_design_scores_gemma":[0.00010041992,0.00041795374,0.06997085,0.0004252467,0.000055241995,0.017331915,0.00020835332,0.00047440105,0.015906708,0.0022676773,0.8928077,0.000033529042],"about_ca_topic_score_codex":0.0007053854,"about_ca_topic_score_gemma":0.0020890464,"teacher_disagreement_score":0.23535356,"about_ca_system_score_codex":0.0001529008,"about_ca_system_score_gemma":0.00014082709,"threshold_uncertainty_score":0.7873361},"labels":[],"label_agreement":null},{"id":"W2035693514","doi":"10.1067/mpd.2003.82","title":"Hypercalciuria in Beckwith-Wiedemann syndrome","year":2003,"lang":"en","type":"article","venue":"The Journal of Pediatrics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","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":"SickKids Foundation; Hospital for Sick Children; University of Toronto","funders":"","keywords":"Nephrocalcinosis; Medicine; Hypercalciuria; Beckwith–Wiedemann syndrome; Gastroenterology; Hyperuricosuria; Internal medicine; Urology; Incidence (geometry); Metabolic disorder; Endocrinology; Urine; Kidney","score_opus":0.009807503404749344,"score_gpt":0.23377623133643285,"score_spread":0.22396872793168351,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2035693514","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.98728323,0.002782088,0.0010902812,0.0010523805,0.00014356269,0.000025480169,0.0002794242,0.00017108185,0.0071724793],"genre_scores_gemma":[0.9981185,0.0005475847,0.00063738116,0.0001404479,0.00009373181,0.000008489825,0.00007660622,0.0000151289905,0.00036206088],"study_design_codex":"case_report","study_design_gemma":"case_report","domain_scores_codex":[0.9996996,0.0000412102,0.000057217643,0.000055277975,0.000058138536,0.000088543966],"domain_scores_gemma":[0.9993363,0.00026267278,0.00014816746,0.000031587013,0.0000434437,0.00017769786],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00018858911,0.0012295428,0.00047665375,0.002473297,0.0007105153,0.0006384952,0.00072574365,0.0018643601,0.0027474654],"category_scores_gemma":[0.0025630898,0.0007002595,0.0003108149,0.0015451219,0.0010953023,0.000574122,0.0007523732,0.0008368056,0.00036537624],"study_design_candidate":"case_report","study_design_consensus":"case_report","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0005114832,0.000053291034,0.057267535,0.00007461842,0.00003863231,0.91928107,0.00025358956,0.00023501158,0.015457332,0.0008498744,0.00082408485,0.0051534246],"study_design_scores_gemma":[0.00007936272,0.00012987222,0.054967258,0.00003493867,0.00014464615,0.9325763,0.00025320664,0.00066151726,0.008391041,0.001059882,0.0016700592,0.000031923802],"about_ca_topic_score_codex":0.0026000475,"about_ca_topic_score_gemma":0.002318683,"teacher_disagreement_score":0.0027474654,"about_ca_system_score_codex":0.0004586759,"about_ca_system_score_gemma":0.00067439163,"threshold_uncertainty_score":0.009191215},"labels":[],"label_agreement":null},{"id":"W2036611166","doi":"10.1002/ajmg.a.30020","title":"<i>CDKN1C</i> mutation in Wiedemann–Beckwith syndrome patients reduces RNA splicing efficiency and identifies a splicing enhancer","year":2004,"lang":"en","type":"article","venue":"American Journal of Medical Genetics Part A","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":10,"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; University of Toronto","funders":"","keywords":"RNA splicing; Beckwith–Wiedemann syndrome; Genetics; Enhancer; Exonic splicing enhancer; Mutation; Biology; RNA; Computational biology; Gene; Gene expression; DNA methylation","score_opus":0.005352674133553476,"score_gpt":0.2548464087881549,"score_spread":0.24949373465460142,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2036611166","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99902594,0.00016339634,0.00028664677,0.000034062115,0.0000068307872,0.000004717261,0.00010439441,0.000022018574,0.00035207986],"genre_scores_gemma":[0.9989569,0.000109453606,0.0006281524,0.000034786426,0.000005734532,0.00000527428,0.000097293065,0.000010622886,0.00015172538],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9998561,0.0000208833,0.000020019366,0.00005307299,0.000028734126,0.00002113902],"domain_scores_gemma":[0.9998636,0.000038344457,0.000048112153,0.0000078029525,0.0000068183685,0.00003527239],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00010274821,0.00063142815,0.00030340638,0.00052275846,0.0002693854,0.00026946116,0.00013614936,0.0004951915,0.0014945214],"category_scores_gemma":[0.00046954033,0.00019626459,0.0002469671,0.00032102127,0.0002691161,0.000100771256,0.00013576148,0.0002582422,0.00020537824],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0014308817,0.00019074639,0.2120885,0.00008716822,0.00019453354,0.039559204,0.0005336565,0.00056977913,0.71969885,0.00045134124,0.0008391368,0.024356298],"study_design_scores_gemma":[0.00015447898,0.0008258762,0.69583744,0.000040914707,0.00026358757,0.15963128,0.00026883633,0.002232948,0.136665,0.00034334062,0.0036872225,0.000049074573],"about_ca_topic_score_codex":0.0014382661,"about_ca_topic_score_gemma":0.0013526756,"teacher_disagreement_score":0.0014945214,"about_ca_system_score_codex":0.00019092509,"about_ca_system_score_gemma":0.00012979892,"threshold_uncertainty_score":0.004999697},"labels":[],"label_agreement":null},{"id":"W2036775365","doi":"10.1159/000268822","title":"No Effect of Parental Age on Risk of Multiple Sclerosis: A Population-Based Study","year":2009,"lang":"en","type":"article","venue":"Neuroepidemiology","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":11,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":true,"ca_institutions":"University of British Columbia","funders":"","keywords":"Medicine; Multiple sclerosis; Population; Pediatrics; Demography; Environmental health; Psychiatry","score_opus":0.0224120161089832,"score_gpt":0.27600682344375904,"score_spread":0.25359480733477585,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2036775365","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9974382,0.00043187093,0.00015874117,0.0000857904,0.000014575184,0.0000130421295,0.0006748118,0.0000073018077,0.0011756134],"genre_scores_gemma":[0.99917454,0.00016105162,0.000083220395,0.00002794209,0.0000063063817,0.0000054108687,0.00028187808,0.0000040541804,0.00025561888],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9983726,0.00031692587,0.00009654103,0.0004979799,0.0003858836,0.0003301456],"domain_scores_gemma":[0.9964849,0.0008496073,0.00082017115,0.0005274579,0.00052211044,0.00079584966],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0015694764,0.0006382567,0.00057623896,0.0011784239,0.0016097649,0.001002779,0.0011998632,0.0008432994,0.00391432],"category_scores_gemma":[0.0059881387,0.00048926513,0.0009517913,0.0018398217,0.00095659285,0.00047835926,0.00069086766,0.00071325275,0.00021565765],"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":[0.00034582836,0.00003391779,0.9975291,0.000010817829,0.00019290872,0.00019241667,0.00020087301,0.000031974134,0.00020893684,0.00005652213,0.00011242837,0.0010844262],"study_design_scores_gemma":[0.000020090241,0.00013806182,0.9988256,0.000010510417,0.00012023455,0.00026322773,0.00016021745,0.00012903185,0.00004367204,0.000034599892,0.00024818254,0.0000066180423],"about_ca_topic_score_codex":0.40368232,"about_ca_topic_score_gemma":0.3021704,"teacher_disagreement_score":0.40368232,"about_ca_system_score_codex":0.0018479616,"about_ca_system_score_gemma":0.003266359,"threshold_uncertainty_score":0.80266523},"labels":[],"label_agreement":null},{"id":"W2038744986","doi":"10.1002/mc.20126","title":"DNA methylation in the CTCF‐binding site I and the expression pattern of the <i>H19</i> gene: Does positive expression predict poor prognosis in early stage head and neck carcinomas?","year":2005,"lang":"en","type":"article","venue":"Molecular Carcinogenesis","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":28,"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; University of Toronto; Ontario Institute for Cancer Research","funders":"Fundação para o Desenvolvimento da UNESP; Coordenação de Aperfeiçoamento de Pessoal de Nível Superior; Division of Materials Research; Fundação de Amparo à Pesquisa do Estado de São Paulo","keywords":"CTCF; Biology; Methylation; Gene silencing; DNA methylation; Genomic imprinting; Imprinting (psychology); Cancer research; Gene; Molecular biology; Chromatin; Gene expression; Genetics; Enhancer","score_opus":0.00651171642146533,"score_gpt":0.2160510322379391,"score_spread":0.20953931581647375,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2038744986","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9994128,0.00030878987,0.00007017744,0.000020552632,0.0000022691459,0.0000027907774,0.000045619756,0.0000019052842,0.00013504858],"genre_scores_gemma":[0.9997061,0.000081020284,0.000041480762,0.0000058622873,0.000007398621,0.0000020338778,0.0000671915,9.318549e-7,0.00008795037],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9998653,0.000033454704,0.000012259327,0.000028032244,0.000029189758,0.000031775264],"domain_scores_gemma":[0.99947613,0.00017712881,0.00016376599,0.000034347813,0.000054375607,0.00009436398],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00035111257,0.00019296058,0.00025880686,0.00071553886,0.00016648506,0.00027983054,0.00023583611,0.0003805945,0.0008599471],"category_scores_gemma":[0.0011154425,0.00016183966,0.00016843177,0.00043918076,0.00031443886,0.00018276263,0.00014575983,0.00026497754,0.0002558954],"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":[0.00044768673,0.000023898141,0.98781675,0.000014623904,0.000048530885,0.000130818,0.000070795424,0.00004375916,0.00790314,0.000008668666,0.000053436186,0.0034378485],"study_design_scores_gemma":[0.000007232448,0.000108221415,0.9979481,0.00000261846,0.000031313335,0.0004943283,0.000062965664,0.0003290687,0.00087860005,0.000018329802,0.000115970615,0.0000032853748],"about_ca_topic_score_codex":0.0035720803,"about_ca_topic_score_gemma":0.0033505207,"teacher_disagreement_score":0.0035720803,"about_ca_system_score_codex":0.0002096347,"about_ca_system_score_gemma":0.00015685966,"threshold_uncertainty_score":0.007102549},"labels":[],"label_agreement":null},{"id":"W2039283181","doi":"10.1203/pdr.0b013e3180457660","title":"Growth Regulation, Imprinted Genes, and Chromosome 11p15.5","year":2007,"lang":"en","type":"review","venue":"Pediatric Research","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":116,"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":"Genomic imprinting; Biology; Epigenetics; Genetics; Imprinting (psychology); Gene; DNA methylation; Beckwith–Wiedemann syndrome; Gene duplication; Gene expression","score_opus":0.08896719396499418,"score_gpt":0.40192033114789316,"score_spread":0.31295313718289897,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2039283181","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":[0.0000908223,0.9982836,0.0001667657,0.00030854106,0.0002254718,0.0000027015517,0.000014806635,0.000010224283,0.0008969389],"genre_scores_gemma":[0.00038101195,0.9985077,0.00017857229,0.000121850186,0.00017100664,0.000004534932,0.000029763636,0.0000010975007,0.00060445204],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.9998294,0.000026402991,0.00002129283,0.000029359147,0.00007599701,0.000017459619],"domain_scores_gemma":[0.9996481,0.0001672911,0.000051343246,0.000009970671,0.00007896058,0.000044296965],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00061276247,0.0012408072,0.0016659416,0.00250119,0.0002842937,0.0008988767,0.0014555315,0.0012132579,0.003603646],"category_scores_gemma":[0.0006355985,0.00034733044,0.000345698,0.0032342672,0.00074874866,0.0011843409,0.00065699365,0.0018303581,0.0030292731],"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":[0.00012059883,0.000056329,0.00032406635,0.006942701,0.0000918936,0.0008211497,0.0000413053,0.00047199175,0.0019594033,0.004314274,0.05626827,0.92858803],"study_design_scores_gemma":[0.00002445632,0.000038891172,0.001051933,0.0014917179,0.00007751306,0.0037028182,0.0000576503,0.000059688802,0.0005037533,0.0022391917,0.9907363,0.000016049542],"about_ca_topic_score_codex":0.0012565204,"about_ca_topic_score_gemma":0.0023425072,"teacher_disagreement_score":0.003603646,"about_ca_system_score_codex":0.0008229143,"about_ca_system_score_gemma":0.0010252319,"threshold_uncertainty_score":0.012055397},"labels":[],"label_agreement":null},{"id":"W2040096570","doi":"10.1038/oby.2005.224","title":"Evaluation of Prader‐Willi Syndrome Gene <i>MAGEL2</i> in Severe Childhood‐Onset Obesity","year":2005,"lang":"en","type":"article","venue":"Obesity Research","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":7,"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":"University of Alberta; Wellcome Trust","keywords":"Obesity; Medicine; Gene; Genomic imprinting; Neurodevelopmental disorder; Internal medicine; Allele; Endocrinology; Genetics; Bioinformatics; Biology; Gene expression","score_opus":0.04253667839914183,"score_gpt":0.3377563221438153,"score_spread":0.29521964374467347,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2040096570","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99784267,0.00030500654,0.0006624611,0.00005596823,0.000009096742,0.000026969343,0.00010974551,0.00001881089,0.00096932356],"genre_scores_gemma":[0.998779,0.00021385615,0.00059514726,0.00004100536,0.00000525163,0.000008399983,0.000102500846,0.000008946615,0.00024596293],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9997898,0.00004759476,0.000020612844,0.00004604401,0.00003972419,0.00005623929],"domain_scores_gemma":[0.9997876,0.00009128954,0.00003205539,0.000007817837,0.000025440137,0.000055772467],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00027138117,0.00053397653,0.00028153087,0.000990339,0.00034851886,0.00020810778,0.0002006991,0.00043974462,0.0009165508],"category_scores_gemma":[0.00053766137,0.00020024092,0.00025335,0.0003032705,0.00049978937,0.00014160741,0.00028412163,0.00036827018,0.00012750481],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0023717363,0.00031120438,0.18782957,0.0001691417,0.0001100435,0.08320016,0.00068568764,0.0009522782,0.71220124,0.00048189407,0.00031650075,0.011370684],"study_design_scores_gemma":[0.00014667687,0.0027764642,0.52910703,0.000047583828,0.00035803643,0.12477573,0.0010012974,0.0031377831,0.33356893,0.00036380562,0.0046648197,0.000051780582],"about_ca_topic_score_codex":0.001482791,"about_ca_topic_score_gemma":0.0012111097,"teacher_disagreement_score":0.001482791,"about_ca_system_score_codex":0.00021635996,"about_ca_system_score_gemma":0.00021023359,"threshold_uncertainty_score":0.0030661225},"labels":[],"label_agreement":null},{"id":"W2040114279","doi":"10.1139/g01-013","title":"Imprinting and deviation from Mendelian transmission ratios","year":2001,"lang":"en","type":"article","venue":"Genome","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":41,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":true,"route_about_ca":false,"ca_institutions":"Royal Victoria Hospital","funders":"McGill University","keywords":"Genomic imprinting; Biology; Imprinting (psychology); Genetics; Allele; Mendelian inheritance; Gene; Gene expression","score_opus":0.009623054575879447,"score_gpt":0.22403843145084426,"score_spread":0.2144153768749648,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2040114279","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9915488,0.0009812294,0.0056051835,0.000071863265,0.0000118400885,0.000011914916,0.00025451832,0.000056318404,0.0014582898],"genre_scores_gemma":[0.99852294,0.00016820218,0.00095401454,0.000018498278,0.0000064216256,0.00000786602,0.00015316793,0.000013013997,0.000155964],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99867934,0.0003927477,0.00010095458,0.00036931984,0.0003501295,0.00010743875],"domain_scores_gemma":[0.99640346,0.0018215326,0.0011979456,0.00032056894,0.00013281265,0.00012374874],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0011089838,0.00030012982,0.00035785793,0.0010485627,0.0002274648,0.0004339046,0.00042061572,0.00029231914,0.001445901],"category_scores_gemma":[0.006536973,0.00018075574,0.00019877883,0.00079799426,0.0007540578,0.0002714601,0.00033800487,0.0005997939,0.00014472542],"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":[0.0013729803,0.000051853523,0.7920984,0.00018313449,0.0005495919,0.0032539067,0.0014354096,0.0036771793,0.13691473,0.0078038713,0.00048661014,0.0521723],"study_design_scores_gemma":[0.000046681787,0.00035768794,0.9412839,0.000025663563,0.00013628068,0.011971452,0.0002519116,0.004438774,0.030804636,0.00864998,0.0019750155,0.000058048907],"about_ca_topic_score_codex":0.0006452746,"about_ca_topic_score_gemma":0.00048387834,"teacher_disagreement_score":0.001445901,"about_ca_system_score_codex":0.00026497652,"about_ca_system_score_gemma":0.00013036779,"threshold_uncertainty_score":0.005864978},"labels":[],"label_agreement":null},{"id":"W2040929679","doi":"10.1074/jbc.m110.162347","title":"Epigenetic Silencing of β-Spectrin, a TGF-β Signaling/Scaffolding Protein in a Human Cancer Stem Cell Disorder","year":2010,"lang":"en","type":"article","venue":"Journal of Biological Chemistry","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":43,"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","funders":"National Institute of Diabetes and Digestive and Kidney Diseases; National Cancer Institute","keywords":"Biology; Epigenetics; Cancer research; Gene silencing; Cancer; Genetics; Cell biology; Gene","score_opus":0.01288980656884443,"score_gpt":0.2508291214340931,"score_spread":0.23793931486524866,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2040929679","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9885461,0.0021922502,0.0064454097,0.00017504448,0.000043140182,0.000026674032,0.00043490337,0.00020695206,0.0019295462],"genre_scores_gemma":[0.994659,0.0014580652,0.0015479028,0.0000834291,0.000016290995,0.000014083805,0.00033530922,0.000019713798,0.0018663876],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.99995244,0.0000052949354,0.00000468323,0.00001495253,0.000016985954,0.0000057578022],"domain_scores_gemma":[0.99994755,0.000005291628,0.000026140968,0.0000054150905,0.0000037060365,0.000011946063],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.000057499456,0.00022998312,0.00011717371,0.0002402259,0.000119753655,0.00014472018,0.00012297394,0.00020838418,0.0010195252],"category_scores_gemma":[0.00007920395,0.00007453313,0.00013632682,0.00012715333,0.00017826808,0.00011489896,0.00022697324,0.00020332362,0.00018784721],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.000029866625,0.000010403456,0.001225939,0.000025427371,0.000008328933,0.00061922066,0.000014377499,0.000046143996,0.9946291,0.00024015873,0.000086641456,0.0030645214],"study_design_scores_gemma":[0.000035281686,0.00036525057,0.07043168,0.000023481249,0.00012093851,0.014633464,0.00009036711,0.0017198512,0.9006145,0.00060950563,0.011342556,0.000013117896],"about_ca_topic_score_codex":0.00023906605,"about_ca_topic_score_gemma":0.0005894253,"teacher_disagreement_score":0.0010195252,"about_ca_system_score_codex":0.00009597658,"about_ca_system_score_gemma":0.00010763872,"threshold_uncertainty_score":0.003410697},"labels":[],"label_agreement":null},{"id":"W2041081418","doi":"10.1159/000350525","title":"Update on Body Composition and Bone Density in Children with Prader-Willi Syndrome","year":2013,"lang":"en","type":"article","venue":"Hormone Research in Paediatrics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":23,"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":"","keywords":"Lean body mass; Medicine; Internal medicine; Endocrinology; Bone mineral; Obesity; Fat mass; Bone density; Body fat percentage; Body weight; Osteoporosis","score_opus":0.014919690099754681,"score_gpt":0.26866408874493014,"score_spread":0.25374439864517545,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2041081418","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":[0.029194767,0.9314085,0.0032397695,0.008407218,0.006028126,0.00014244033,0.008574449,0.00038199613,0.012622674],"genre_scores_gemma":[0.08616276,0.8668054,0.008407071,0.0059898463,0.009188368,0.00031773496,0.014422766,0.00006814457,0.008637966],"study_design_codex":"design_other","study_design_gemma":"observational","domain_scores_codex":[0.9994567,0.000108906184,0.0001378883,0.00008196488,0.00018192787,0.000032597156],"domain_scores_gemma":[0.9978655,0.0008345006,0.00022978769,0.000050067883,0.00090822496,0.0001119316],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0008184485,0.000838336,0.001455259,0.0024140095,0.0001762981,0.0007559518,0.0008401477,0.0010245446,0.0021491302],"category_scores_gemma":[0.00218211,0.0003165582,0.00057383016,0.0015105372,0.00017806489,0.0007742097,0.0004456836,0.0012480891,0.0009581357],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0007013781,0.00020250118,0.056472525,0.008595924,0.0008851748,0.0012098617,0.0001878459,0.00043052356,0.0026470632,0.000405674,0.14445682,0.7838048],"study_design_scores_gemma":[0.00019229452,0.0006394797,0.2626608,0.008003951,0.0022803668,0.010064531,0.0004049171,0.00062487053,0.002088103,0.0006087134,0.7123447,0.000087319735],"about_ca_topic_score_codex":0.006131862,"about_ca_topic_score_gemma":0.00855941,"teacher_disagreement_score":0.006131862,"about_ca_system_score_codex":0.00043359262,"about_ca_system_score_gemma":0.00051612593,"threshold_uncertainty_score":0.012192309},"labels":[],"label_agreement":null},{"id":"W2041342968","doi":"10.1515/jpem.2000.13.s1.845","title":"Gonadotropin-dependent Sexual Precocity in a Boy Affected by Pseudohypoparathyroidism","year":2000,"lang":"en","type":"article","venue":"Journal of Pediatric Endocrinology and Metabolism","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":1,"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","keywords":"Pseudohypoparathyroidism; Hyperphosphatemia; Internal medicine; Medicine; Endocrinology; Precocious puberty; Basal (medicine); Vitamin D and neurology; Gynecomastia; Testosterone (patch); Thyroid; Hormone; Parathyroid hormone; Calcium","score_opus":0.006460576607177535,"score_gpt":0.23201299209491064,"score_spread":0.2255524154877331,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2041342968","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99384016,0.00088460406,0.0005803713,0.0008907781,0.00010887355,0.00005983202,0.0002006892,0.000057516685,0.0033770988],"genre_scores_gemma":[0.99855775,0.0003644984,0.00029216477,0.00015769254,0.00009296375,0.000010244436,0.000054013824,0.00001112805,0.00045962151],"study_design_codex":"case_report","study_design_gemma":"case_report","domain_scores_codex":[0.99950933,0.00005828328,0.000030148516,0.00013060732,0.000088226305,0.00018351275],"domain_scores_gemma":[0.99903405,0.00030698482,0.00015267626,0.00003605165,0.00004449586,0.00042574882],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00020036753,0.0014334448,0.0010703753,0.0014948829,0.002158198,0.0009829589,0.00063101965,0.0020505134,0.0018671891],"category_scores_gemma":[0.0018871282,0.0011667418,0.00065763365,0.0010242464,0.0015273868,0.00068943907,0.0008911518,0.0025579056,0.00041034812],"study_design_candidate":"case_report","study_design_consensus":"case_report","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00003719971,0.00004743725,0.012429249,0.000023996236,0.0000060503257,0.98483235,0.00038419905,0.00006694511,0.0011536668,0.00014698326,0.00015634876,0.0007156295],"study_design_scores_gemma":[0.000026039723,0.00023778898,0.031263113,0.000012943124,0.000015273738,0.9666725,0.0003215193,0.00020225224,0.0005519278,0.00012132768,0.00056053646,0.000014830705],"about_ca_topic_score_codex":0.0045633772,"about_ca_topic_score_gemma":0.0040822653,"teacher_disagreement_score":0.0045633772,"about_ca_system_score_codex":0.00079952803,"about_ca_system_score_gemma":0.0007669529,"threshold_uncertainty_score":0.009073675},"labels":[],"label_agreement":null},{"id":"W2041665669","doi":"10.1038/ejhg.2015.38","title":"Two novel disease-causing variants in BMPR1B are associated with brachydactyly type A1","year":2015,"lang":"en","type":"article","venue":"European Journal of Human Genetics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":25,"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; Ottawa Hospital; Children's Hospital of Eastern Ontario; University of Ottawa","funders":"Graduate School, University of Maryland","keywords":"Brachydactyly; Biology; Frameshift mutation; Genetics; Noggin; Phenotype; Anatomy; Bone morphogenetic protein; Gene; Endocrinology","score_opus":0.043439506672161135,"score_gpt":0.2688178148046308,"score_spread":0.22537830813246967,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2041665669","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99531883,0.000583974,0.0010385859,0.00030721864,0.000069710375,0.0000765315,0.0004091889,0.000053740798,0.0021421316],"genre_scores_gemma":[0.9972337,0.0001914021,0.0011191415,0.0001658007,0.000070263304,0.000027999633,0.0002834559,0.000020530932,0.0008877575],"study_design_codex":"case_report","study_design_gemma":"observational","domain_scores_codex":[0.99954045,0.00004839872,0.00005050475,0.00014297776,0.0001278246,0.00008981585],"domain_scores_gemma":[0.9993782,0.00016519644,0.00015411474,0.000025916639,0.000039940307,0.00023653235],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00022573251,0.001995023,0.00063209323,0.0018875002,0.00084581826,0.0005290673,0.0007332336,0.002315731,0.0028903917],"category_scores_gemma":[0.0014039262,0.00046419358,0.000629443,0.0007904544,0.00078340294,0.00028120735,0.00071710144,0.0010078317,0.00053358934],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00067289855,0.00035176973,0.073768094,0.00016188569,0.00013465589,0.81075704,0.0011413737,0.00043932945,0.10129082,0.001364457,0.0011077955,0.00880987],"study_design_scores_gemma":[0.00016684405,0.00037679903,0.14016807,0.000064543674,0.00008935878,0.8453417,0.00022667323,0.00093649654,0.008360605,0.0004616216,0.0037452343,0.000062049614],"about_ca_topic_score_codex":0.0016146831,"about_ca_topic_score_gemma":0.0015693667,"teacher_disagreement_score":0.0028903917,"about_ca_system_score_codex":0.00039575735,"about_ca_system_score_gemma":0.00029314385,"threshold_uncertainty_score":0.009669304},"labels":[],"label_agreement":null},{"id":"W2043170079","doi":"10.1016/j.ydbio.2003.10.017","title":"Murine numb regulates granule cell maturation in the cerebellum","year":2003,"lang":"en","type":"article","venue":"Developmental Biology","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":44,"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; Direction de l’hospitalisation et de l’offre de Soins; McGill University; U.S. Department of Energy","keywords":"NUMB; Biology; Granule cell; Cerebellum; Cell biology; Neurogenesis; Progenitor cell; Notch signaling pathway; Centrosome; Granule (geology); Neuroscience; Stem cell; Cell; Signal transduction; Central nervous system; Cell cycle; Genetics; Dentate gyrus","score_opus":0.00725058020780578,"score_gpt":0.2146110699844447,"score_spread":0.20736048977663893,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2043170079","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99565965,0.0009366647,0.0018244168,0.0000699045,0.000014956506,0.0000035563796,0.00010435675,0.00008534392,0.0013011018],"genre_scores_gemma":[0.99670166,0.00029095748,0.0009721808,0.000015802023,0.0000032494206,0.000005123956,0.00008177714,0.000052897725,0.001876459],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99982435,0.000028606457,0.000017378017,0.000045770394,0.000045607478,0.000038207676],"domain_scores_gemma":[0.9996166,0.000048890553,0.00017066937,0.000040132556,0.000024394496,0.00009928339],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00013704968,0.00029658136,0.00025237218,0.0006256504,0.00025627823,0.0004963954,0.00032029705,0.0003817385,0.0009621484],"category_scores_gemma":[0.00026252173,0.00039827172,0.000119915705,0.00017843302,0.0004906324,0.00038700286,0.00037486549,0.00047038883,0.00050814584],"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":[0.000107182525,0.0000050498684,0.00055048114,0.000009971866,0.0000029269406,0.00015600692,0.000019964751,0.00009878044,0.9978162,0.00044193087,0.000022101052,0.0007692791],"study_design_scores_gemma":[0.000029079247,0.00007466149,0.022219777,0.000011897416,0.000017447986,0.0007723902,0.000078046185,0.0010361116,0.9734929,0.00047532105,0.0017856425,0.000006631819],"about_ca_topic_score_codex":0.0010489218,"about_ca_topic_score_gemma":0.0016843242,"teacher_disagreement_score":0.0010489218,"about_ca_system_score_codex":0.00083166093,"about_ca_system_score_gemma":0.0002146336,"threshold_uncertainty_score":0.0060341954},"labels":[],"label_agreement":null},{"id":"W2046155010","doi":"10.1126/science.1228633","title":"An Exon Splice Enhancer Primes IGF2:IGF2R Binding Site Structure and Function Evolution","year":2012,"lang":"en","type":"article","venue":"Science","topic":"Genetic Syndromes and Imprinting","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":"Canada's Michael Smith Genome Sciences Centre","funders":"Cancer Research UK; Wellcome Trust","keywords":"Enhancer; Exon; splice; Function (biology); Genetics; Computational biology; Biology; Gene; Transcription factor","score_opus":0.006335964942303857,"score_gpt":0.24666241209349718,"score_spread":0.24032644715119333,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2046155010","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9932192,0.00032541808,0.0038573255,0.000084384366,0.00000894813,0.00000501014,0.00005938898,0.00006288737,0.0023773473],"genre_scores_gemma":[0.99623543,0.00013059023,0.0021894448,0.000046824374,0.0000073635897,0.0000029035828,0.00007588939,0.000013398684,0.0012982166],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99995506,0.0000062575186,0.0000024949152,0.000016671953,0.000010190593,0.000009328647],"domain_scores_gemma":[0.9998987,0.000034658275,0.000023651866,0.000011636678,0.000011959681,0.000019552423],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0001274229,0.000145559,0.00009244185,0.00014792447,0.00013707216,0.00015207173,0.00015587307,0.00029728087,0.0020182205],"category_scores_gemma":[0.00013971345,0.00008013552,0.00009178097,0.00009483935,0.00020120607,0.00013112504,0.0001739472,0.00025493617,0.00029139008],"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":[0.0000495184,0.000008854586,0.0031153997,0.000015519206,0.000003411228,0.00016466607,0.000038947623,0.00017858163,0.989135,0.0008871335,0.00002708666,0.006375877],"study_design_scores_gemma":[0.000042309555,0.00039476148,0.21653704,0.00002981733,0.000053696283,0.0044373074,0.00019123602,0.006695632,0.7521908,0.0017508642,0.017648902,0.000027609656],"about_ca_topic_score_codex":0.0005767747,"about_ca_topic_score_gemma":0.0010144303,"teacher_disagreement_score":0.0020182205,"about_ca_system_score_codex":0.00030736864,"about_ca_system_score_gemma":0.00016816363,"threshold_uncertainty_score":0.006751597},"labels":[],"label_agreement":null},{"id":"W2046258358","doi":"10.1016/j.jpag.2008.01.026","title":"Incipient/Premature Ovarian Failure in a Teenage Girl with the Van Wyk Grumbach Syndrome","year":2008,"lang":"en","type":"article","venue":"Journal of Pediatric and Adolescent Gynecology","topic":"Genetic Syndromes and Imprinting","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":"Children's Hospital of Eastern Ontario; University of Ottawa","funders":"","keywords":"Medicine; Premature ovarian failure; Ovarian hyperstimulation syndrome; Girl; Controlled ovarian hyperstimulation; Pediatrics; Gynecology; Population; Pregnancy; Infertility","score_opus":0.006194630991661926,"score_gpt":0.20220537655381443,"score_spread":0.1960107455621525,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2046258358","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9939965,0.00083201134,0.0008929359,0.0016908697,0.00013695803,0.000054910965,0.00010472404,0.000070188275,0.0022207864],"genre_scores_gemma":[0.9981596,0.0004417024,0.00056976854,0.00017070412,0.000106920124,0.000015303622,0.000047241934,0.000015542217,0.00047325515],"study_design_codex":"case_report","study_design_gemma":"case_report","domain_scores_codex":[0.9996942,0.00004396085,0.00003495035,0.000058525122,0.000069320915,0.00009903131],"domain_scores_gemma":[0.99894637,0.00040561164,0.00023377305,0.000043542117,0.0000514546,0.0003193026],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00024522867,0.001096916,0.0009689286,0.0020856704,0.00126772,0.00067109487,0.0009181166,0.0023494498,0.0015335884],"category_scores_gemma":[0.00348239,0.0006249836,0.00064938125,0.0009787822,0.0011650714,0.00069901004,0.0009384052,0.0022835275,0.00022403625],"study_design_candidate":"case_report","study_design_consensus":"case_report","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00003602803,0.000039480317,0.01729413,0.000012538296,0.0000064509245,0.97973216,0.00019662056,0.00006588395,0.001169834,0.00023790998,0.00013090597,0.0010780804],"study_design_scores_gemma":[0.00002077385,0.00012911731,0.017622294,0.000012974564,0.000020902804,0.98055446,0.00020184413,0.00026922036,0.00057501305,0.00023732141,0.00034363967,0.000012478874],"about_ca_topic_score_codex":0.0030255297,"about_ca_topic_score_gemma":0.002588111,"teacher_disagreement_score":0.0030255297,"about_ca_system_score_codex":0.00045138074,"about_ca_system_score_gemma":0.0007363394,"threshold_uncertainty_score":0.006015837},"labels":[],"label_agreement":null},{"id":"W2046632949","doi":"10.1002/ajmg.a.20458","title":"Boy with 47,XXY,del(15)(q11.2q13) karyotype and Prader–Willi syndrome: A new case and review of the literature","year":2003,"lang":"en","type":"review","venue":"American Journal of Medical Genetics Part A","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","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":"Kingston General Hospital; Queen's University; McMaster University; Hamilton Health Sciences; Hamilton Regional Laboratory Medicine Program","funders":"","keywords":"Karyotype; Genetic counseling; Genetics; Chromosome analysis; Chromosome; Phenotype; Biology; Gene","score_opus":0.01306908285347114,"score_gpt":0.29288358884756444,"score_spread":0.2798145059940933,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2046632949","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":[0.017435564,0.97297084,0.0013335388,0.0012910386,0.00091383484,0.00002949643,0.00007095551,0.000079792335,0.0058749844],"genre_scores_gemma":[0.05453903,0.93761593,0.0015672719,0.0011216351,0.0016590356,0.000028970346,0.000121886675,0.000012730801,0.0033334778],"study_design_codex":"design_other","study_design_gemma":"case_report","domain_scores_codex":[0.99977976,0.000030143789,0.00004675329,0.00005524056,0.000055511642,0.00003255509],"domain_scores_gemma":[0.9997427,0.000116938594,0.000055202076,0.000011931366,0.00002871862,0.000044517066],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00026885196,0.0010098197,0.0016102744,0.0024901074,0.00035216875,0.0006889884,0.00078204914,0.0014350058,0.0020031645],"category_scores_gemma":[0.0006260638,0.00038240818,0.00028959927,0.0018606891,0.0007276166,0.0015348924,0.0004694459,0.0008025289,0.0015752218],"study_design_candidate":"case_report","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00012718781,0.00019733212,0.009583211,0.006364081,0.00012528118,0.35444045,0.0004886859,0.00044798304,0.0034026937,0.0013667551,0.03054233,0.59291404],"study_design_scores_gemma":[0.000027726617,0.000121231526,0.009143651,0.0010035693,0.00011779851,0.847756,0.00038363689,0.00013521826,0.00055396307,0.0007278663,0.13999003,0.000039257502],"about_ca_topic_score_codex":0.00085157854,"about_ca_topic_score_gemma":0.0016603653,"teacher_disagreement_score":0.0024901074,"about_ca_system_score_codex":0.00029918816,"about_ca_system_score_gemma":0.00057829753,"threshold_uncertainty_score":0.006701231},"labels":[],"label_agreement":null},{"id":"W2047164593","doi":"10.1159/000213487","title":"Increased Nuchal Translucency and Other Ultrasound Findings in a Case of Simpson-Golabi-Behmel Syndrome","year":2008,"lang":"en","type":"article","venue":"Fetal Diagnosis and Therapy","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","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":"McMaster University Medical Centre","funders":"","keywords":"Medicine; Macroglossia; Polyhydramnios; Nuchal Translucency Measurement; Proband; Prenatal diagnosis; Fetal echocardiography; Fetus; Craniosynostosis; Obstetrics; Gestation; Nuchal translucency; Pregnancy; Anatomy; Pathology; Tongue; Genetics; Mutation","score_opus":0.015762748595486802,"score_gpt":0.243726719434031,"score_spread":0.2279639708385442,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2047164593","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9981724,0.00044647005,0.00026485062,0.00016204809,0.000011228205,0.000009662394,0.00003223106,0.000017000406,0.00088405964],"genre_scores_gemma":[0.9993105,0.00015345827,0.00033417286,0.00004172703,0.00002455187,0.0000027126039,0.000018515058,0.0000036881281,0.00011062411],"study_design_codex":"case_report","study_design_gemma":"case_report","domain_scores_codex":[0.999716,0.00005336884,0.00003222747,0.000062351784,0.000064354,0.00007176278],"domain_scores_gemma":[0.99915767,0.0003464455,0.00017126146,0.00003643586,0.000029119987,0.00025914612],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00027143967,0.00056000333,0.00037073068,0.0018338076,0.00055241125,0.0004382131,0.00027765083,0.0011428518,0.0015074163],"category_scores_gemma":[0.0024808059,0.0005519655,0.00020381603,0.00050876697,0.0011722964,0.00031565168,0.00058664405,0.00053205685,0.00023710908],"study_design_candidate":"case_report","study_design_consensus":"case_report","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.000100514146,0.000027959699,0.049251836,0.000029370869,0.000011820132,0.9407988,0.00037547215,0.00007906935,0.006820373,0.00014292073,0.000121726094,0.0022401446],"study_design_scores_gemma":[0.00002147654,0.00008373053,0.03594596,0.000009010057,0.000010719612,0.96205866,0.00012855153,0.00021489419,0.0012466019,0.00009379763,0.00017928286,0.000007308084],"about_ca_topic_score_codex":0.0024545253,"about_ca_topic_score_gemma":0.0017577485,"teacher_disagreement_score":0.0024545253,"about_ca_system_score_codex":0.00047158168,"about_ca_system_score_gemma":0.00037771245,"threshold_uncertainty_score":0.0050427318},"labels":[],"label_agreement":null},{"id":"W2047811624","doi":"10.1016/s0304-3835(00)00347-5","title":"Loss of IGF-II imprinting in endometrial tumors: overexpression in carcinosarcoma","year":2000,"lang":"en","type":"article","venue":"Cancer Letters","topic":"Genetic Syndromes and Imprinting","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":"University of Toronto; St. Michael's Hospital","funders":"Medical Research Council","keywords":"Carcinosarcoma; Endometrium; Biology; Endometrial cancer; Cancer research; Imprinting (psychology); Endocrinology; Gene; Internal medicine; Cancer; Carcinoma; Medicine; Genetics","score_opus":0.009034487653785363,"score_gpt":0.24710054909120052,"score_spread":0.23806606143741516,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2047811624","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99103105,0.0021690016,0.0020482894,0.0008494661,0.000079821955,0.0000066608654,0.00031944647,0.00013542027,0.0033606747],"genre_scores_gemma":[0.99687934,0.000776935,0.0006977311,0.000051015584,0.000046366084,0.0000055021164,0.00014461522,0.000012160165,0.0013863394],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99994135,0.0000094351335,0.000010197823,0.000008033499,0.000018117502,0.0000128173715],"domain_scores_gemma":[0.99974805,0.00010319654,0.000039353727,0.000024725656,0.000034244073,0.00005052425],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00016594667,0.00019236282,0.00013158597,0.00073152845,0.00015510005,0.00030970774,0.00017846825,0.00031845496,0.0009885037],"category_scores_gemma":[0.00042634137,0.00013613755,0.000082811646,0.0003496567,0.00028188244,0.000184808,0.00015589524,0.0002197312,0.0002948039],"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":[0.0019960261,0.00003409956,0.046949364,0.00014893337,0.00003800828,0.026923785,0.00024659417,0.00036562543,0.89578086,0.0016100705,0.0015198188,0.024386806],"study_design_scores_gemma":[0.00007657852,0.00050054473,0.1686889,0.00001695952,0.00010604169,0.04711749,0.00043123655,0.0014612912,0.76304144,0.0013058948,0.01722642,0.000027250544],"about_ca_topic_score_codex":0.0008440446,"about_ca_topic_score_gemma":0.0007544535,"teacher_disagreement_score":0.0009885037,"about_ca_system_score_codex":0.00024440777,"about_ca_system_score_gemma":0.00016952145,"threshold_uncertainty_score":0.0033069253},"labels":[],"label_agreement":null},{"id":"W2047876270","doi":"10.1007/s00467-013-2461-4","title":"Bone metabolism in the fetus and neonate","year":2013,"lang":"en","type":"review","venue":"Pediatric Nephrology","topic":"Genetic Syndromes and Imprinting","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":"Health Sciences Centre","funders":"","keywords":"Internal medicine; Fetus; Endocrinology; Medicine; Calcitriol; Calcium metabolism; Fetal circulation; Parathyroid hormone; Bone remodeling; Calcium; Calcitonin; Placenta; Pregnancy; Biology","score_opus":0.017632468209040082,"score_gpt":0.2702975116756923,"score_spread":0.25266504346665225,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2047876270","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":[0.00011272421,0.9990395,0.000110528745,0.00021619086,0.00008939595,0.0000010410819,0.000010419952,0.0000035009775,0.00041665282],"genre_scores_gemma":[0.0008412348,0.99834406,0.00015390711,0.00011864664,0.00022300688,0.0000022609934,0.000017676199,0.0000011094047,0.00029810955],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.999811,0.00003170707,0.00003320446,0.000038023816,0.00006869751,0.000017344306],"domain_scores_gemma":[0.999603,0.0002159869,0.00006216283,0.000010709531,0.00007181628,0.00003625801],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0004277566,0.00075503025,0.0015028901,0.0020876771,0.00021510257,0.0008314434,0.0008416229,0.0013233003,0.0014332674],"category_scores_gemma":[0.0009697307,0.00034187487,0.00032776018,0.002010145,0.00062991556,0.0007103477,0.0006936544,0.0013895539,0.00092818984],"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":[0.00009123171,0.00003936961,0.000891086,0.0073036095,0.00008682349,0.0018886054,0.000039914834,0.00043753753,0.0018955597,0.0022397211,0.021641737,0.9634447],"study_design_scores_gemma":[0.000033179087,0.00008866052,0.0038288946,0.004472286,0.00024712668,0.022798384,0.00015290687,0.00024163739,0.001147845,0.003815048,0.9631273,0.00004659315],"about_ca_topic_score_codex":0.0021451244,"about_ca_topic_score_gemma":0.0036552348,"teacher_disagreement_score":0.0021451244,"about_ca_system_score_codex":0.00063290104,"about_ca_system_score_gemma":0.0012272783,"threshold_uncertainty_score":0.004794717},"labels":[],"label_agreement":null},{"id":"W2047900106","doi":"10.1007/s00427-008-0267-3","title":"Genomic Imprinting in Drosophila has properties of both mammalian and insect imprinting","year":2008,"lang":"en","type":"article","venue":"Development Genes and Evolution","topic":"Genetic Syndromes and Imprinting","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":"National Research Council Canada; Dalhousie University; Mount Allison University","funders":"","keywords":"Genomic imprinting; Imprinting (psychology); Biology; Genetics; Drosophila melanogaster; Gene silencing; Gene; Somatic cell; DNA methylation; Gene expression","score_opus":0.026688093591510816,"score_gpt":0.2013895589304301,"score_spread":0.17470146533891928,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2047900106","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.97219694,0.005594657,0.0135498755,0.00020860844,0.000042256142,0.000010512208,0.00043816643,0.00021091977,0.007748016],"genre_scores_gemma":[0.99361706,0.0014307293,0.0026542265,0.000032471136,0.00001274164,0.0000046367422,0.00021821423,0.000014171028,0.0020156724],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99996316,0.0000041573353,0.00000252177,0.000010450664,0.000013082754,0.0000066700345],"domain_scores_gemma":[0.99994576,0.000009627582,0.000021423291,0.000007360929,0.0000042446463,0.0000115567345],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00004953546,0.00020514318,0.000118637196,0.00027826856,0.00012461105,0.00030203984,0.00015382502,0.00014589443,0.000535539],"category_scores_gemma":[0.00008701738,0.00012396302,0.00009418199,0.00021336773,0.0003424666,0.00022841105,0.0001851477,0.00021494039,0.00015336952],"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":[0.00010175011,0.0000044743115,0.0021859868,0.000059495334,0.000011405284,0.00028623475,0.00003533174,0.00038814,0.9780522,0.006099153,0.000075259086,0.01270059],"study_design_scores_gemma":[0.000019073397,0.00011157679,0.06395076,0.000008479362,0.000037954018,0.001493368,0.00005402241,0.0010532865,0.91915476,0.0023072588,0.011795635,0.000013883274],"about_ca_topic_score_codex":0.0008309254,"about_ca_topic_score_gemma":0.0018546485,"teacher_disagreement_score":0.0008309254,"about_ca_system_score_codex":0.0002611572,"about_ca_system_score_gemma":0.00013225619,"threshold_uncertainty_score":0.0018948317},"labels":[],"label_agreement":null},{"id":"W2048726057","doi":"10.1136/bcr-2013-202729","title":"Prolonged spontaneous normocalcaemia in pseudohypoparathyroidism from resorption of soft tissue calcium deposits: a cautionary tale","year":2014,"lang":"en","type":"article","venue":"BMJ Case Reports","topic":"Genetic Syndromes and Imprinting","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":"University of Calgary","funders":"","keywords":"Medicine; Pseudohypoparathyroidism; Hypocalcaemia; Calcium; Calcitriol; Parathyroid hormone; Hyperphosphatemia; Internal medicine; Osteodystrophy; Soft tissue; Calcinosis; Calcification; Endocrinology; Surgery","score_opus":0.010873681568878631,"score_gpt":0.2665576406642031,"score_spread":0.2556839590953245,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2048726057","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.8912137,0.02333821,0.0069350484,0.05219488,0.0025010356,0.00021455163,0.00031009997,0.00037135388,0.022921199],"genre_scores_gemma":[0.98600674,0.003689893,0.0011625007,0.003685569,0.003985311,0.000026387392,0.000045903176,0.000043153184,0.0013544003],"study_design_codex":"case_report","study_design_gemma":"case_report","domain_scores_codex":[0.99919766,0.00019913132,0.00013137059,0.0001462646,0.00014124389,0.00018424363],"domain_scores_gemma":[0.9962276,0.0022495834,0.0006100061,0.0002935616,0.0001469826,0.0004722822],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00085082307,0.0011454304,0.0007793769,0.0015579774,0.0017348124,0.0018310926,0.0015360307,0.006879427,0.0014927939],"category_scores_gemma":[0.0075274943,0.00061972847,0.0008280062,0.0010866454,0.0033011686,0.0015948404,0.0015649318,0.004081424,0.000556958],"study_design_candidate":"case_report","study_design_consensus":"case_report","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.000028606722,0.000008071967,0.0030426907,0.00002971963,0.000005189558,0.9951438,0.00012226067,0.000032235806,0.00023968499,0.00022557114,0.00033903937,0.0007831677],"study_design_scores_gemma":[0.000015187973,0.00002642794,0.0020630334,0.000029965404,0.000011813952,0.9953933,0.0002118315,0.00014055095,0.00023035289,0.0006399701,0.0012267382,0.0000109436805],"about_ca_topic_score_codex":0.0018986173,"about_ca_topic_score_gemma":0.001965157,"teacher_disagreement_score":0.006879427,"about_ca_system_score_codex":0.0010107538,"about_ca_system_score_gemma":0.0006543227,"threshold_uncertainty_score":0.0073336363},"labels":[],"label_agreement":null},{"id":"W2050173466","doi":"10.3109/17518423.2012.676101","title":"Neurodevelopmental outcomes in children with Angelman syndrome after 1 year of behavioural intervention","year":2012,"lang":"en","type":"article","venue":"Developmental Neurorehabilitation","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":15,"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; Hamilton Health Sciences; McMaster Children's Hospital","funders":"Hamilton Health Sciences","keywords":"Angelman syndrome; Intervention (counseling); Cognition; Psychology; Randomized controlled trial; Clinical psychology; Pediatrics; Medicine; Physical therapy; Psychiatry","score_opus":0.00925460367021961,"score_gpt":0.22461933935163925,"score_spread":0.21536473568141964,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2050173466","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9996879,0.00011329156,0.000012061025,0.000022694381,0.000005237544,0.00001807917,0.000037511643,0.0000036510323,0.000099661964],"genre_scores_gemma":[0.99931276,0.0001547792,0.00011557656,0.000014810031,0.0000054472666,0.00006560881,0.00018444296,0.0000010803321,0.0001455348],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99959475,0.00009823129,0.000029065512,0.000046258814,0.000085678446,0.00014598043],"domain_scores_gemma":[0.99946374,0.00008117448,0.00019237955,0.000024909714,0.000056353005,0.0001813869],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00091746816,0.00045306608,0.00089400634,0.00041226763,0.00043913306,0.00026317735,0.00041881186,0.0004329601,0.0006828408],"category_scores_gemma":[0.002047896,0.00011364326,0.0006523178,0.00034195863,0.00037378672,0.00029006018,0.00044571824,0.0004805562,0.00009785872],"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":[0.027325207,0.03868606,0.78847754,0.0006879823,0.000795543,0.0027890122,0.003972001,0.0016908933,0.007354392,0.00019552857,0.0020147278,0.12601107],"study_design_scores_gemma":[0.0012235094,0.030341044,0.964501,0.000055695215,0.00021739383,0.0005283928,0.00090344035,0.00026110007,0.0012405305,0.000042830332,0.00066368934,0.000021330141],"about_ca_topic_score_codex":0.011857282,"about_ca_topic_score_gemma":0.012664233,"teacher_disagreement_score":0.011857282,"about_ca_system_score_codex":0.0007772249,"about_ca_system_score_gemma":0.0010683067,"threshold_uncertainty_score":0.023576498},"labels":[],"label_agreement":null},{"id":"W2050466071","doi":"10.1101/gr.077115.108","title":"Comparative analysis of human chromosome 7q21 and mouse proximal chromosome 6 reveals a placental-specific imprinted gene, <i>TFPI2</i>/<i>Tfpi2</i>, which requires EHMT2 and EED for allelic-silencing","year":2008,"lang":"en","type":"article","venue":"Genome Research","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":86,"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","funders":"Medical Research Council; Sickkids Research Institute; Medical Research Council Canada; Agence Nationale de la Recherche; Hospital for Sick Children; Wellcome Trust; Genome Canada; Wellbeing of Women; March of Dimes Foundation","keywords":"Biology; Genomic imprinting; Histone; Genetics; DNA methylation; Imprinting (psychology); Molecular biology; Histone methylation; Gene; Gene expression","score_opus":0.07297829103464612,"score_gpt":0.3466313032178899,"score_spread":0.2736530121832438,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2050466071","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9767853,0.0059069474,0.009042052,0.0001728973,0.00003759068,0.000057090132,0.002500435,0.0002542781,0.0052432637],"genre_scores_gemma":[0.9721505,0.0021694007,0.011634612,0.00010794621,0.000029369683,0.00009532217,0.009344777,0.000038815964,0.004429299],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9998814,0.00001075319,0.0000045061706,0.00005061867,0.000035540856,0.000017237024],"domain_scores_gemma":[0.9998852,0.000026362697,0.000041786283,0.000012783376,0.000008356507,0.00002550992],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.000110782814,0.00036638323,0.0002623316,0.0008554641,0.00020511972,0.00015765154,0.0002879504,0.00026944396,0.005152598],"category_scores_gemma":[0.00016816347,0.00022255277,0.00048674326,0.00034979923,0.00017450789,0.0001050342,0.00030891862,0.0002995515,0.0010704676],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00051566033,0.000021935784,0.003948101,0.000097636825,0.00009043202,0.00068310805,0.000052095125,0.00017302208,0.9815388,0.0006920983,0.00021282771,0.011974318],"study_design_scores_gemma":[0.00028178038,0.0016303812,0.4169252,0.0000952789,0.00040065934,0.020004168,0.00015994377,0.0032857212,0.49360287,0.0024562655,0.061109543,0.00004816583],"about_ca_topic_score_codex":0.000842964,"about_ca_topic_score_gemma":0.0010823837,"teacher_disagreement_score":0.005152598,"about_ca_system_score_codex":0.0002172389,"about_ca_system_score_gemma":0.00014583212,"threshold_uncertainty_score":0.017237186},"labels":[],"label_agreement":null},{"id":"W2050592293","doi":"10.1093/humrep/dem268","title":"A survey of assisted reproductive technology births and imprinting disorders","year":2007,"lang":"en","type":"article","venue":"Human Reproduction","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":165,"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":"Hospital for Sick Children","keywords":"Genomic imprinting; Imprinting (psychology); Angelman syndrome; Assisted reproductive technology; Allele; Epigenetics; Medicine; Cohort; Uniparental disomy; Genetics; Pregnancy; Gene; Biology; Internal medicine; DNA methylation; Infertility; Chromosome","score_opus":0.017189344132017354,"score_gpt":0.2766048440626119,"score_spread":0.25941549993059454,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2050592293","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9983936,0.00016626192,0.000068672256,0.00006455845,0.000004374811,0.000025281066,0.00087371405,0.0000039493584,0.00039956725],"genre_scores_gemma":[0.9982717,0.00035588426,0.00011631408,0.000090992355,0.000008277102,0.000037153,0.000559699,0.0000016207701,0.000558232],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9991627,0.00021983158,0.00011950063,0.00015588796,0.00021346346,0.00012865668],"domain_scores_gemma":[0.9976084,0.00049288286,0.0010676763,0.00012770256,0.0003228862,0.0003804275],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0006804318,0.00016975404,0.0002452053,0.0009136865,0.00028593172,0.00033287678,0.00046005935,0.00037848653,0.0021333576],"category_scores_gemma":[0.002517277,0.00026784034,0.00020305491,0.0011191827,0.00040971625,0.00035037127,0.00044568614,0.0003251868,0.00039802425],"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":[0.000019899873,0.000019507383,0.99720734,0.00002863391,0.000009557666,0.0002788409,0.0004359796,0.000019432851,0.00037276983,0.000020778578,0.00025468317,0.0013325285],"study_design_scores_gemma":[0.0000028340282,0.00012717338,0.9976605,0.000010663938,0.0000045728843,0.000825947,0.000720074,0.00003878724,0.00008430581,0.0000041977955,0.0005177062,0.0000031687503],"about_ca_topic_score_codex":0.018055838,"about_ca_topic_score_gemma":0.011576659,"teacher_disagreement_score":0.018055838,"about_ca_system_score_codex":0.0005847457,"about_ca_system_score_gemma":0.00046639034,"threshold_uncertainty_score":0.035901487},"labels":[],"label_agreement":null},{"id":"W2050939151","doi":"10.1007/s10549-008-0042-1","title":"Mutations of the MYH gene do not substantially contribute to the risk of breast cancer","year":2008,"lang":"en","type":"article","venue":"Breast Cancer Research and Treatment","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":46,"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; Women's College Hospital; University of Toronto","funders":"","keywords":"Breast cancer; Gene; Medicine; Oncology; Cancer; Genetics; Mutation; Biology; Internal medicine; Cancer research","score_opus":0.02861996030288757,"score_gpt":0.31702780802881747,"score_spread":0.2884078477259299,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2050939151","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9955383,0.00096643553,0.00055804936,0.00023525572,0.00004705801,0.0000072194366,0.00019754693,0.000025880561,0.00242407],"genre_scores_gemma":[0.9988341,0.00020894459,0.00014707595,0.00003093924,0.000045356508,0.0000020232799,0.00010577149,0.0000062053755,0.0006194881],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9996123,0.00011508746,0.00003567328,0.000064083986,0.000117806005,0.000055148306],"domain_scores_gemma":[0.9987741,0.0004993262,0.00032517675,0.00015295434,0.000072343246,0.00017608613],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00036879527,0.0002637737,0.00033439844,0.0006664136,0.000193201,0.0002448306,0.00035746957,0.0005165824,0.0029809123],"category_scores_gemma":[0.0023528074,0.00018052563,0.00024218942,0.0003421794,0.00038381724,0.00027753678,0.00027482386,0.00039541986,0.000396496],"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":[0.0053027994,0.00017791243,0.81685615,0.00008601232,0.00037073594,0.0047087893,0.00014985715,0.00040991412,0.13266164,0.001393613,0.0007781834,0.037104394],"study_design_scores_gemma":[0.00007831839,0.00058426964,0.9661519,0.000015868825,0.00018647996,0.014405287,0.00007985836,0.00047268986,0.014527084,0.0008521593,0.0026334166,0.000012765412],"about_ca_topic_score_codex":0.00047048635,"about_ca_topic_score_gemma":0.00043049981,"teacher_disagreement_score":0.0029809123,"about_ca_system_score_codex":0.00014019254,"about_ca_system_score_gemma":0.00011007708,"threshold_uncertainty_score":0.009972155},"labels":[],"label_agreement":null},{"id":"W2051494278","doi":"10.1002/ajmg.a.32144","title":"Paternal deletion 6q24.3: A new congenital anomaly syndrome associated with intrauterine growth failure, early developmental delay and characteristic facial appearance","year":2008,"lang":"en","type":"article","venue":"American Journal of Medical Genetics Part A","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":25,"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; McMaster University","funders":"","keywords":"Biology; Frontal Bossing; Genetics; Brachycephaly; Phenotype; Genomic imprinting; Short stature; Breakpoint; Anatomy; Chromosome; Gene; Gene expression; Skull","score_opus":0.008252025591810189,"score_gpt":0.20964208383381613,"score_spread":0.20139005824200595,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2051494278","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9902378,0.0007063764,0.0062604044,0.00035007673,0.00006779186,0.000030432351,0.00035981828,0.00016327006,0.0018241322],"genre_scores_gemma":[0.9954015,0.0003724262,0.0027505702,0.00010738678,0.00009211156,0.000016044827,0.00023573858,0.000028927248,0.0009952475],"study_design_codex":"case_report","study_design_gemma":"case_report","domain_scores_codex":[0.99978346,0.00002654427,0.000018180546,0.000080893056,0.000053771608,0.000037132057],"domain_scores_gemma":[0.99948776,0.00012809537,0.0001752672,0.000031767693,0.00002775596,0.00014927016],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.000108073364,0.0015025645,0.00049269234,0.00056205114,0.00058422686,0.00035834732,0.0005439825,0.00069171196,0.0020548326],"category_scores_gemma":[0.0009107058,0.00041801832,0.0003366826,0.00045528766,0.00073327794,0.00023926995,0.00059310696,0.0007473176,0.00043064103],"study_design_candidate":"case_report","study_design_consensus":"case_report","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00044545767,0.00009890043,0.12475135,0.00019147697,0.00010982833,0.7284357,0.00091799884,0.000728913,0.1149247,0.0017852588,0.0014779596,0.026132446],"study_design_scores_gemma":[0.00004887836,0.00018156062,0.054664392,0.00001335912,0.000058247995,0.93533874,0.00008711332,0.0004827812,0.006522191,0.000303962,0.0022756436,0.000023186072],"about_ca_topic_score_codex":0.00088674226,"about_ca_topic_score_gemma":0.0012299599,"teacher_disagreement_score":0.0020548326,"about_ca_system_score_codex":0.00020015884,"about_ca_system_score_gemma":0.00026469651,"threshold_uncertainty_score":0.006874144},"labels":[],"label_agreement":null},{"id":"W2051574088","doi":"10.1002/ajmg.a.31323","title":"Constitutional UPD for chromosome 11p15 in individuals with isolated hemihyperplasia is associated with high tumor risk and occurs following assisted reproductive technologies","year":2006,"lang":"en","type":"article","venue":"American Journal of Medical Genetics Part A","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":83,"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; Ontario Institute for Cancer Research; University of Toronto","funders":"Canadian Institutes of Health Research","keywords":"Genomic imprinting; Epigenetics; Wilms' tumor; Methylation; DNA methylation; Uniparental disomy; Cancer research; Beckwith–Wiedemann syndrome; Biology; Tumor progression; Cancer; Internal medicine; Chromosome; Karyotype; Oncology; Gene; Genetics; Medicine","score_opus":0.006484700487838024,"score_gpt":0.24059588803180695,"score_spread":0.23411118754396892,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2051574088","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9988154,0.00022063505,0.0002121153,0.000033309097,0.000006261926,0.000006155221,0.0001184411,0.000009160072,0.0005784954],"genre_scores_gemma":[0.9995478,0.0000794176,0.00011921379,0.000009666678,0.000008407339,0.000002467723,0.00008080915,0.0000015858113,0.00015047763],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9996606,0.00007177529,0.000030622075,0.00012671987,0.000059532184,0.000050644285],"domain_scores_gemma":[0.99923444,0.00024557597,0.0003174609,0.000057197725,0.000036374222,0.0001090579],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00024250321,0.0003659061,0.00028542895,0.001196518,0.0005520928,0.00029327415,0.0002368689,0.0004598877,0.0029327674],"category_scores_gemma":[0.0013196882,0.00019816191,0.00021161158,0.00093584985,0.00049598794,0.00017354547,0.00041067178,0.0004361254,0.0002217485],"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":[0.00047453676,0.0000391057,0.9720641,0.000032675405,0.000068941554,0.01058449,0.00025161533,0.00010791438,0.0081429,0.0001848947,0.00020730776,0.007841462],"study_design_scores_gemma":[0.000010163798,0.00018882283,0.95960635,0.000015238529,0.000054196757,0.03738233,0.00020773383,0.00020379713,0.0015529202,0.00016584936,0.00060150266,0.000011115708],"about_ca_topic_score_codex":0.0014085479,"about_ca_topic_score_gemma":0.0012376043,"teacher_disagreement_score":0.0029327674,"about_ca_system_score_codex":0.00016316556,"about_ca_system_score_gemma":0.00015347428,"threshold_uncertainty_score":0.009811044},"labels":[],"label_agreement":null},{"id":"W2051640192","doi":"10.4161/rdis.24421","title":"Leptin signaling defects in a mouse model of Prader-Willi syndrome","year":2013,"lang":"en","type":"article","venue":"Rare Diseases","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":11,"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":"Alberta Heritage Foundation for Medical Research; University of Alberta; Canadian Institutes of Health Research; Women and Children's Health Research Institute; Children's Health Research Institute","keywords":"Leptin; Cell biology; Internal medicine; Chemistry; Endocrinology; Neuroscience; Biology; Medicine; Obesity","score_opus":0.011602234532805683,"score_gpt":0.2238802197965938,"score_spread":0.21227798526378813,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2051640192","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9632803,0.0038825728,0.016298259,0.002616162,0.00070388534,0.00038109586,0.0043574017,0.0014503148,0.007030032],"genre_scores_gemma":[0.9457267,0.005470111,0.019903066,0.0006884044,0.00012438787,0.0012857795,0.003112697,0.00035526537,0.023333663],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9992981,0.00012549543,0.00009473821,0.00020212687,0.00018087527,0.00009877537],"domain_scores_gemma":[0.99945253,0.00008371517,0.00017014006,0.000060844457,0.000039387745,0.00019333433],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0005218128,0.0014332463,0.00058327016,0.0021266788,0.00062606024,0.000773109,0.0011968269,0.0021746506,0.005407182],"category_scores_gemma":[0.00043997585,0.000812885,0.00081959576,0.0006115417,0.0009961952,0.0007099119,0.00077171926,0.0027870717,0.0017409074],"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":[0.00068539486,0.0005876773,0.0007127737,0.00011877148,0.000058294325,0.0018883382,0.00014564041,0.0005159466,0.987626,0.0031403915,0.00074418104,0.0037764926],"study_design_scores_gemma":[0.001451446,0.0048600915,0.0152274165,0.0003136629,0.00042600013,0.013334938,0.00050065335,0.010542619,0.8978276,0.0031630679,0.052216016,0.00013653087],"about_ca_topic_score_codex":0.0011487998,"about_ca_topic_score_gemma":0.0019832077,"teacher_disagreement_score":0.005407182,"about_ca_system_score_codex":0.0007638592,"about_ca_system_score_gemma":0.0006423175,"threshold_uncertainty_score":0.018088818},"labels":[],"label_agreement":null},{"id":"W2052272439","doi":"10.1007/s10024-005-1154-9","title":"Beckwith-Wiedemann Syndrome: Historical, Clinicopathological, and Etiopathogenetic Perspectives","year":2005,"lang":"en","type":"review","venue":"Pediatric and Developmental Pathology","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":197,"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":"","keywords":"Beckwith–Wiedemann syndrome; Macroglossia; Medicine; Omphalocele; Hemihypertrophy; Wilms' tumor; Rhabdomyosarcoma; Haploinsufficiency; Hydronephrosis; Costello syndrome; Pediatrics; Hepatoblastoma; Pathology; Anatomy; Internal medicine; Pregnancy; Cancer; Tongue; Fetus; Genetics; Sarcoma; Biology","score_opus":0.030959401645255777,"score_gpt":0.29186141433675933,"score_spread":0.26090201269150354,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2052272439","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":[0.00087918644,0.9963934,0.00019694991,0.00045132337,0.00020867807,0.0000018342281,0.000008028291,0.0000075276103,0.0018530905],"genre_scores_gemma":[0.0055517554,0.99299663,0.00029643642,0.00026404654,0.00031869963,0.0000033329688,0.000016236476,8.9352585e-7,0.00055207236],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.99991596,0.000019665524,0.000014362107,0.00001806318,0.000019645691,0.000012371728],"domain_scores_gemma":[0.9998635,0.00006358143,0.000022903943,0.0000045184747,0.000028132918,0.00001734338],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00027992687,0.0006857576,0.0007017857,0.0023304783,0.00026837637,0.00062491535,0.0005168326,0.00072154903,0.0012593109],"category_scores_gemma":[0.00040976002,0.00019176508,0.00020510779,0.0022380853,0.00064528384,0.0016687933,0.00036847583,0.0008987902,0.0006387816],"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":[0.00014704808,0.000080460515,0.005284662,0.0061238175,0.00010490528,0.0153950555,0.00036118104,0.00067914766,0.002422281,0.010051842,0.025666893,0.9336826],"study_design_scores_gemma":[0.000020030388,0.00010040212,0.0096024135,0.003902782,0.000175061,0.108873926,0.00058442244,0.00020694357,0.0006758707,0.0055023935,0.87031466,0.00004104775],"about_ca_topic_score_codex":0.00085925177,"about_ca_topic_score_gemma":0.0021597894,"teacher_disagreement_score":0.0023304783,"about_ca_system_score_codex":0.0006169524,"about_ca_system_score_gemma":0.0005107046,"threshold_uncertainty_score":0.004476309},"labels":[],"label_agreement":null},{"id":"W2052515804","doi":"10.4161/epi.25812","title":"Quantitative DNA methylation analysis improves epigenotype-phenotype correlations in Beckwith-Wiedemann syndrome","year":2013,"lang":"en","type":"article","venue":"Epigenetics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","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":"Pediatric Oncology Group","funders":"","keywords":"Beckwith–Wiedemann syndrome; DNA methylation; Methylation; Biology; Epigenetics; Reproductive technology; Macroglossia; Genetics; Internal medicine; Endocrinology; Pathology; Pregnancy; Medicine; Gene","score_opus":0.013296094425825944,"score_gpt":0.2591895653496462,"score_spread":0.24589347092382027,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2052515804","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99850035,0.00021991391,0.0009327348,0.0000120903405,0.000001601277,0.0000039910537,0.00007491769,0.000017031618,0.00023748381],"genre_scores_gemma":[0.9988362,0.00007139898,0.0009078184,0.000008749566,0.0000021561402,0.0000044478966,0.000098220706,0.0000042416023,0.000066790606],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9996679,0.00012746498,0.00003617243,0.00007837178,0.00005985078,0.000030275874],"domain_scores_gemma":[0.9995944,0.00019947444,0.000095617106,0.00003161307,0.000040200266,0.000038858347],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0003270641,0.00024636294,0.00018391044,0.0008051985,0.0000848858,0.00016989606,0.00008922877,0.00018105622,0.0006179099],"category_scores_gemma":[0.0016106149,0.00012350063,0.00010088028,0.00026440242,0.0001388858,0.000086188986,0.00018993388,0.00016563288,0.000120810575],"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":[0.00064382365,0.00004097072,0.8121533,0.00003922603,0.00007795844,0.00093739777,0.00020086112,0.00048489196,0.1616731,0.00006756708,0.00009379777,0.023587087],"study_design_scores_gemma":[0.0000092946875,0.00024048386,0.97096395,0.000006267336,0.00004334615,0.005011572,0.00006905602,0.0015081387,0.021698557,0.00007248765,0.00036664866,0.000010099059],"about_ca_topic_score_codex":0.00041244493,"about_ca_topic_score_gemma":0.00055358483,"teacher_disagreement_score":0.0008051985,"about_ca_system_score_codex":0.000093630384,"about_ca_system_score_gemma":0.000051322804,"threshold_uncertainty_score":0.0020671487},"labels":[],"label_agreement":null},{"id":"W2053330159","doi":"10.1002/ajmg.a.32030","title":"Severe presentation of Beckwith–Wiedemann syndrome associated with high levels of constitutional paternal uniparental disomy for chromosome 11p15","year":2007,"lang":"en","type":"article","venue":"American Journal of Medical Genetics Part A","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":49,"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 Medical Centre; Hospital for Sick Children; University of Toronto","funders":"Canadian Institutes of Health Research","keywords":"Beckwith–Wiedemann syndrome; Macroglossia; Hepatoblastoma; Uniparental disomy; Medicine; Gigantism; Genetics; Biology; Internal medicine; Karyotype; Chromosome; Pathology; DNA methylation; Gene","score_opus":0.015576308560413263,"score_gpt":0.2805095904989016,"score_spread":0.26493328193848836,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2053330159","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99504423,0.00038519673,0.0013614187,0.00027224366,0.000037439622,0.000025793766,0.00013160535,0.000070150505,0.0026719116],"genre_scores_gemma":[0.9990464,0.00015345824,0.00039170345,0.00009559558,0.000040504325,0.000005177492,0.00006288659,0.000009029431,0.00019529676],"study_design_codex":"case_report","study_design_gemma":"case_report","domain_scores_codex":[0.9996954,0.000045826335,0.00002869818,0.00008287796,0.000061070765,0.00008618273],"domain_scores_gemma":[0.99929476,0.000143388,0.00014387604,0.000034791916,0.000029718121,0.00035350444],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00017549522,0.0017492108,0.00069729873,0.0011133373,0.00073218683,0.0005278715,0.00032245493,0.00080247497,0.0010891416],"category_scores_gemma":[0.0012127357,0.0005344391,0.00040062654,0.000633666,0.0008521204,0.0004728729,0.0010697963,0.0009133379,0.0001994587],"study_design_candidate":"case_report","study_design_consensus":"case_report","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0002466565,0.000054715914,0.09528644,0.000089213456,0.00007810025,0.8622763,0.00075806055,0.0004280143,0.032588318,0.00082746026,0.0006773226,0.0066893892],"study_design_scores_gemma":[0.000021903543,0.00024206119,0.06921024,0.000011789331,0.000034949528,0.925716,0.00017255043,0.00031923567,0.0033296752,0.00026225598,0.00064194563,0.000037305937],"about_ca_topic_score_codex":0.0009887537,"about_ca_topic_score_gemma":0.0013377806,"teacher_disagreement_score":0.0017492108,"about_ca_system_score_codex":0.00029570243,"about_ca_system_score_gemma":0.00031025536,"threshold_uncertainty_score":0.0036435723},"labels":[],"label_agreement":null},{"id":"W2053631009","doi":"10.1111/j.1528-1167.2006.00969.x","title":"Lamotrigine Therapy of Epilepsy with Angelman's Syndrome","year":2007,"lang":"en","type":"article","venue":"Epilepsia","topic":"Genetic Syndromes and Imprinting","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":"Centre Hospitalier Universitaire Sainte-Justine; Université de Montréal; Hôpital Notre-Dame","funders":"","keywords":"Lamotrigine; Carbamazepine; Medicine; Valproic Acid; Phenytoin; Clonazepam; Levetiracetam; Epilepsy; Topiramate; Tolerability; Pediatrics; Angelman syndrome; Generalized epilepsy; Anesthesia; Oxcarbazepine; Adverse effect; Internal medicine; Psychiatry","score_opus":0.00889768180664113,"score_gpt":0.2369867826109439,"score_spread":0.22808910080430278,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2053631009","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9853183,0.009763561,0.00042371033,0.00040040794,0.000043092434,0.000058233814,0.00008512917,0.000029382672,0.0038781909],"genre_scores_gemma":[0.9973373,0.0016965559,0.00023989094,0.00019678712,0.000038408583,0.000022828259,0.000108655855,0.0000021943686,0.00035742318],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9998605,0.000054692813,0.00002047291,0.000015120905,0.000023719678,0.00002542768],"domain_scores_gemma":[0.9998282,0.000049378767,0.000062037645,0.0000055463343,0.000008206994,0.000046623845],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00023888265,0.00027423783,0.0003439434,0.00023047376,0.00031493208,0.00016524781,0.00020296258,0.0003021519,0.0011452531],"category_scores_gemma":[0.0007738641,0.000060021426,0.0002323536,0.00023053221,0.00024950807,0.00016221308,0.00021292795,0.00029101718,0.00018749594],"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":[0.0051037576,0.0007790655,0.60911715,0.00084035617,0.00048771716,0.15721768,0.0008729918,0.001177273,0.030194646,0.0011273703,0.0043301503,0.18875183],"study_design_scores_gemma":[0.0016067411,0.008840595,0.61105037,0.00038697728,0.00029608866,0.33451548,0.0006668175,0.0020374744,0.01028868,0.00072038017,0.029556464,0.000033942444],"about_ca_topic_score_codex":0.000837538,"about_ca_topic_score_gemma":0.0024707115,"teacher_disagreement_score":0.0011452531,"about_ca_system_score_codex":0.00042744217,"about_ca_system_score_gemma":0.0003737361,"threshold_uncertainty_score":0.0038312078},"labels":[],"label_agreement":null},{"id":"W2054408230","doi":"10.1016/j.celrep.2015.02.011","title":"Loss-of-Function Mutation in APC2 Causes Sotos Syndrome Features","year":2015,"lang":"en","type":"article","venue":"Cell Reports","topic":"Genetic Syndromes and Imprinting","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":"McGill University; McGill University and Génome Québec Innovation Centre; McGill Genome Centre","funders":"Ministry of Education, Culture, Sports, Science and Technology; Hamad Medical Corporation; Qatar Foundation","keywords":"Sotos syndrome; Intellectual disability; Frameshift mutation; Haploinsufficiency; Gene knockdown; Loss function; Mutation; Biology; Kabuki syndrome; Exon; Exome sequencing; Gene; Genetics; Bioinformatics; Phenotype","score_opus":0.013061462145936016,"score_gpt":0.24165785369586984,"score_spread":0.22859639154993383,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2054408230","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9982089,0.00012819795,0.0006220465,0.000035592122,0.00001287399,0.0000105496765,0.00020842704,0.000035395693,0.0007380365],"genre_scores_gemma":[0.9982882,0.00018532533,0.00068265316,0.000023578286,0.0000122705305,0.000012277976,0.00023662254,0.000015898671,0.00054317067],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9998933,0.000012866209,0.000013257875,0.000027370248,0.000036235942,0.00001697012],"domain_scores_gemma":[0.9998535,0.000025394302,0.000047729114,0.000010623076,0.000007762497,0.000055089116],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00005687531,0.00071639655,0.00027457086,0.0005593224,0.00020205986,0.00015711504,0.00018977532,0.00042892442,0.0013706798],"category_scores_gemma":[0.00022778253,0.00016900788,0.00023051309,0.00023741266,0.0003830839,0.00011979398,0.000435842,0.00023366326,0.0002650076],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00029347584,0.000039127273,0.013402542,0.00008601128,0.000045571684,0.06476783,0.00011132565,0.00021444118,0.9165185,0.00059029565,0.0002604616,0.0036704778],"study_design_scores_gemma":[0.0002082872,0.0005612497,0.21735689,0.00004457153,0.00021734936,0.3441884,0.00036718813,0.0030540337,0.42192444,0.0011328018,0.010869288,0.00007557408],"about_ca_topic_score_codex":0.0005517075,"about_ca_topic_score_gemma":0.00079367316,"teacher_disagreement_score":0.0013706798,"about_ca_system_score_codex":0.00016146574,"about_ca_system_score_gemma":0.00017818277,"threshold_uncertainty_score":0.0045853257},"labels":[],"label_agreement":null},{"id":"W2054749794","doi":"10.1002/ajmg.a.31800","title":"Placental mesenchymal dysplasia associated with fetal overgrowth and mosaic deletion of the maternal copy of 11p15.5","year":2007,"lang":"en","type":"article","venue":"American Journal of Medical Genetics Part A","topic":"Genetic Syndromes and Imprinting","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":"University of British Columbia","funders":"Canadian Institutes of Health Research","keywords":"Fetus; Intrauterine growth restriction; Placenta; Uniparental disomy; Biology; Dysplasia; Fetal growth; Beckwith–Wiedemann syndrome; Gene duplication; Andrology; Medicine; Pregnancy; Genetics; Gene; Karyotype; Chromosome","score_opus":0.004601525110106319,"score_gpt":0.2339378782255773,"score_spread":0.229336353115471,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2054749794","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9932767,0.0012723492,0.0024692728,0.00015996103,0.00001757915,0.000025327958,0.00014346871,0.00008828353,0.0025471044],"genre_scores_gemma":[0.99819165,0.00047654397,0.0008333289,0.000023010374,0.000015943318,0.0000055703963,0.000045505607,0.000005550944,0.00040278345],"study_design_codex":"case_report","study_design_gemma":"case_report","domain_scores_codex":[0.99987936,0.00001891833,0.0000104765995,0.00003494469,0.00003098234,0.000025267116],"domain_scores_gemma":[0.99971944,0.00006294402,0.0001389509,0.000021553044,0.000007611053,0.000049410697],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00008510067,0.00054764684,0.00021493301,0.00096190226,0.00022222432,0.00021124448,0.00025937552,0.0003887843,0.0012040862],"category_scores_gemma":[0.00065400347,0.00032128982,0.00016576005,0.00043784644,0.00058011466,0.00013357811,0.00046583766,0.0003277386,0.00016696852],"study_design_candidate":"case_report","study_design_consensus":"case_report","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00031933916,0.000029241159,0.03670161,0.00018316276,0.000066131804,0.8036058,0.00028720044,0.0004216013,0.14071928,0.0015250912,0.00026164117,0.015879966],"study_design_scores_gemma":[0.00002341161,0.00012674146,0.08300088,0.000017325412,0.000049230835,0.89787847,0.00007410213,0.00041297617,0.01685199,0.0004695935,0.0010847436,0.000010617793],"about_ca_topic_score_codex":0.0009771223,"about_ca_topic_score_gemma":0.0012618636,"teacher_disagreement_score":0.0012040862,"about_ca_system_score_codex":0.0002116225,"about_ca_system_score_gemma":0.00016781123,"threshold_uncertainty_score":0.0040280223},"labels":[],"label_agreement":null},{"id":"W205517805","doi":"10.1007/978-3-642-17426-1_8","title":"The Strategies of the Genes: Genomic Conflicts, Attachment Theory, and Development of the Social Brain","year":2011,"lang":"en","type":"book-chapter","venue":"","topic":"Genetic Syndromes and Imprinting","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":"Simon Fraser University","funders":"","keywords":"Psychology; Maladaptation; Offspring; Schizophrenia (object-oriented programming); Developmental psychology; Genomic imprinting; Epigenetics; Autism; Attachment theory; Psychosis; Psychiatry; Genetics; Biology; Gene; DNA methylation","score_opus":0.020445739118320597,"score_gpt":0.24979530169838704,"score_spread":0.22934956258006645,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W205517805","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":[0.054620758,0.29357862,0.038026255,0.057118766,0.0014283194,0.000053409745,0.00010248536,0.00010447013,0.554967],"genre_scores_gemma":[0.675531,0.15340547,0.028931113,0.0054151923,0.001721959,0.00017489049,0.00012196581,0.00008245602,0.13461587],"study_design_codex":"theoretical_or_conceptual","study_design_gemma":"theoretical_or_conceptual","domain_scores_codex":[0.99976236,0.00010175459,0.0000075834773,0.000031411848,0.00007255308,0.00002429158],"domain_scores_gemma":[0.99976283,0.0001601836,0.000019006577,0.000013144933,0.00001574104,0.000029210018],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0006921653,0.0004492495,0.00035825797,0.00047497448,0.0007625166,0.0023771194,0.00083767524,0.0014756232,0.0032353513],"category_scores_gemma":[0.0012701264,0.00020492852,0.00014271871,0.0005418347,0.008451239,0.0028481637,0.0009524299,0.0017750849,0.00046786448],"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":[0.00001766117,0.00001139281,0.0002944643,0.000050306902,0.000007191422,0.0001500375,0.0019672015,0.00032571092,0.0010905052,0.92745554,0.0079846,0.060645424],"study_design_scores_gemma":[0.000008472008,0.000015528245,0.001220022,0.00011091438,0.000005473315,0.00047236818,0.0013738384,0.00040355965,0.000364393,0.9313511,0.06465947,0.000014821027],"about_ca_topic_score_codex":0.001458668,"about_ca_topic_score_gemma":0.0031467285,"teacher_disagreement_score":0.0032353513,"about_ca_system_score_codex":0.0010793605,"about_ca_system_score_gemma":0.00074279483,"threshold_uncertainty_score":0.010823309},"labels":[],"label_agreement":null},{"id":"W2055529397","doi":"10.1016/j.mce.2014.03.003","title":"Modulation of imprinted gene expression following superovulation","year":2014,"lang":"en","type":"article","venue":"Molecular and Cellular Endocrinology","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":61,"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":"Canadian Institutes of Health Research","keywords":"Genomic imprinting; Biology; Imprinting (psychology); Embryo; Placenta; Ovulation; Andrology; Gene expression; Gestation; Gene; Endocrinology; Fetus; Spontaneous conception; Internal medicine; Genetics; Pregnancy; DNA methylation; Medicine; In vitro fertilisation","score_opus":0.005959176298004178,"score_gpt":0.21483477426686473,"score_spread":0.20887559796886054,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2055529397","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9909689,0.002582919,0.00229717,0.00020774774,0.00012478561,0.000033655357,0.0005352009,0.000078861696,0.0031707473],"genre_scores_gemma":[0.99303997,0.0006720137,0.00065987237,0.00013591042,0.00006021155,0.00004546155,0.0006234104,0.000043901946,0.004719249],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9998184,0.000031907388,0.000008600722,0.00003250854,0.000029630966,0.00007899685],"domain_scores_gemma":[0.9994343,0.00024845934,0.00006451945,0.00006720161,0.00004169234,0.00014376226],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0002169938,0.00025558769,0.0004786795,0.0003551299,0.00015973956,0.0005397229,0.00033956586,0.00027292946,0.003073154],"category_scores_gemma":[0.0005456005,0.00019623166,0.0002985701,0.00028427906,0.00047346103,0.00048232923,0.00043550562,0.0010217236,0.0004706714],"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":[0.0015017529,0.000031123836,0.00049883936,0.00002288103,0.000006170915,0.0000856663,0.00004708217,0.00004736432,0.99547297,0.000247683,0.000041242765,0.001997126],"study_design_scores_gemma":[0.000032896238,0.0006532628,0.021112287,0.000007903368,0.000017452427,0.00009728798,0.0001456182,0.00070155784,0.97588056,0.00024646733,0.0010944016,0.00001021832],"about_ca_topic_score_codex":0.0008187641,"about_ca_topic_score_gemma":0.0012576112,"teacher_disagreement_score":0.003073154,"about_ca_system_score_codex":0.00043992742,"about_ca_system_score_gemma":0.00026944987,"threshold_uncertainty_score":0.010280728},"labels":[],"label_agreement":null},{"id":"W2055538355","doi":"10.1016/j.ydbio.2009.09.023","title":"An imprinted GFP insertion reveals long-range epigenetic regulation in embryonic lineages","year":2009,"lang":"en","type":"article","venue":"Developmental Biology","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":8,"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; Agence Nationale pour la Gestion des Déchets Radioactifs; Canada Research Chairs; Michael Smith Health Research BC","keywords":"Biology; Genomic imprinting; Imprinting (psychology); Epigenetics; Genetics; Allele; DNA methylation; Gene; Gene silencing; Gene expression","score_opus":0.010725525482593498,"score_gpt":0.2654735012324604,"score_spread":0.2547479757498669,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2055538355","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9719464,0.0005906686,0.022499572,0.00036210573,0.00008384631,0.000027237063,0.00078241987,0.00046380327,0.0032438538],"genre_scores_gemma":[0.9832719,0.00031132303,0.008681357,0.00013696821,0.000021775644,0.000029473602,0.0006670776,0.00024648377,0.006633705],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99973696,0.000028757016,0.000028911449,0.0000652545,0.00007705544,0.00006295551],"domain_scores_gemma":[0.9993273,0.00026087023,0.00013799279,0.00008302588,0.00003181977,0.00015909174],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00024983278,0.0003554493,0.00026646338,0.00061763666,0.0002579973,0.0004436621,0.00078781456,0.00070288614,0.002539899],"category_scores_gemma":[0.00031700035,0.0004111328,0.00034970252,0.00024962611,0.00072840607,0.0004196671,0.00068993063,0.0016092759,0.0007914501],"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":[0.000039918603,0.00000923569,0.00017094058,0.000007797327,0.0000027462918,0.00017441416,0.000013728041,0.00007073235,0.99834085,0.00051521487,0.000021638576,0.0006328114],"study_design_scores_gemma":[0.00001615026,0.000052114392,0.005510556,0.000004969634,0.000012858844,0.0006196816,0.00003918071,0.0012569381,0.9909656,0.00018470199,0.0013313924,0.00000589622],"about_ca_topic_score_codex":0.0010618905,"about_ca_topic_score_gemma":0.0028267133,"teacher_disagreement_score":0.002539899,"about_ca_system_score_codex":0.00052248745,"about_ca_system_score_gemma":0.00035865064,"threshold_uncertainty_score":0.008496821},"labels":[],"label_agreement":null},{"id":"W2058376960","doi":"10.1002/ajmg.c.30064","title":"Risk of tumorigenesis in overgrowth syndromes: A comprehensive review","year":2005,"lang":"en","type":"review","venue":"American Journal of Medical Genetics Part C Seminars in Medical Genetics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":277,"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":"","keywords":"Sotos syndrome; Head circumference; Wilms' tumor; Medicine; Pediatrics; Gigantism; Internal medicine; Oncology; Biology; Genetics; Birth weight","score_opus":0.02377447417847817,"score_gpt":0.3496704162534198,"score_spread":0.32589594207494166,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2058376960","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":[0.0001456234,0.9990109,0.00006357716,0.0001803762,0.00010004131,0.0000028977468,0.000020463864,0.000005620965,0.00047044855],"genre_scores_gemma":[0.00075656304,0.99869245,0.00012947849,0.00009337126,0.00011211168,0.000004169929,0.000034216893,7.8722593e-7,0.00017686053],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.9998264,0.000032334257,0.000034271918,0.000033401055,0.00006027829,0.000013291902],"domain_scores_gemma":[0.9995516,0.00023815387,0.000066289096,0.00000977658,0.000099120174,0.000035010777],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0005132586,0.0009849205,0.0018992318,0.0029618049,0.00019741678,0.0007044781,0.0009101345,0.00090419035,0.0028511852],"category_scores_gemma":[0.0010032128,0.00030468008,0.00045023384,0.003019792,0.0003464869,0.0011124721,0.0004040533,0.0008907324,0.0010886099],"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":[0.00011194957,0.00006324229,0.0009455593,0.01380389,0.00016191305,0.00058252556,0.00004872089,0.0003871821,0.0004934882,0.001048085,0.038374834,0.94397867],"study_design_scores_gemma":[0.00007143144,0.00021569524,0.0088777775,0.014562623,0.0006358648,0.009541543,0.00016712856,0.00023442296,0.00045477328,0.0019145564,0.9632709,0.00005330808],"about_ca_topic_score_codex":0.0017437829,"about_ca_topic_score_gemma":0.0022657951,"teacher_disagreement_score":0.0029618049,"about_ca_system_score_codex":0.0005773608,"about_ca_system_score_gemma":0.0008935678,"threshold_uncertainty_score":0.009538174},"labels":[],"label_agreement":null},{"id":"W2059877822","doi":"10.1074/jbc.m111.242479","title":"Latent Transforming Growth Factor β-Binding Proteins-2 and -3 Inhibit the Proprotein Convertase 5/6A","year":2011,"lang":"en","type":"article","venue":"Journal of Biological Chemistry","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":20,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Montreal Clinical Research Institute","funders":"Canadian Institutes of Health Research","keywords":"Endoplasmic reticulum; Furin; Proprotein Convertases; Zymogen; Secretory pathway; Proprotein convertase; Cell biology; Biochemistry; Biology; Protein precursor; Golgi apparatus; Chemistry; LDL receptor; Enzyme","score_opus":0.0304132524043616,"score_gpt":0.224037293452257,"score_spread":0.1936240410478954,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2059877822","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.98764056,0.0032529547,0.0057457965,0.000100885205,0.00004531287,0.000034801942,0.00039457137,0.00013160848,0.0026534037],"genre_scores_gemma":[0.9882228,0.0017098811,0.0031975769,0.000073974086,0.0000148306,0.000063022984,0.00086916,0.00003586896,0.0058129053],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99984765,0.000018679242,0.000011566416,0.000026105423,0.000052217645,0.00004374417],"domain_scores_gemma":[0.999845,0.000023046332,0.00005229126,0.000018796705,0.00001576932,0.000045049608],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00011981614,0.0004277456,0.00016133259,0.0002575952,0.00009673646,0.00029471342,0.00016123541,0.00020352591,0.0013430461],"category_scores_gemma":[0.0001191226,0.00013978049,0.00037161194,0.00008867302,0.00015954838,0.00013361964,0.00016420252,0.0005369165,0.0005970345],"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":[0.000084196065,0.000014588057,0.00015035488,0.000013927205,0.0000031999198,0.00002331514,0.000005376559,0.000015338286,0.9987525,0.00005418824,0.000015218199,0.00086779555],"study_design_scores_gemma":[0.000017609997,0.00025814597,0.0044202106,0.0000052755827,0.000011139655,0.00019042732,0.000015955586,0.00037577003,0.9925895,0.00005014497,0.0020641114,0.0000017982401],"about_ca_topic_score_codex":0.0005312891,"about_ca_topic_score_gemma":0.000637894,"teacher_disagreement_score":0.0013430461,"about_ca_system_score_codex":0.0002028517,"about_ca_system_score_gemma":0.00021744054,"threshold_uncertainty_score":0.0044929385},"labels":[],"label_agreement":null},{"id":"W2060000733","doi":"10.1159/000090828","title":"Lessons from comparative analysis of species-specific imprinted genes","year":2006,"lang":"en","type":"review","venue":"Cytogenetic and Genome Research","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":20,"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; University of Toronto","funders":"","keywords":"Biology; Genomic imprinting; Imprinting (psychology); Gene; Genetics; Evolutionary biology; Evolution of mammals; DNA methylation; Gene expression","score_opus":0.23716001289428498,"score_gpt":0.4401018496342546,"score_spread":0.2029418367399696,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2060000733","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":[0.00024411237,0.9967349,0.00043091064,0.0009579861,0.00024363023,0.0000015490688,0.000013386009,0.000008272978,0.001365179],"genre_scores_gemma":[0.0024291743,0.9952609,0.0005392832,0.00067423005,0.00034340832,0.0000049658734,0.00002914278,0.000004754199,0.0007140779],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.9996288,0.000070348884,0.00004031499,0.00012095138,0.00011619639,0.000023384697],"domain_scores_gemma":[0.999212,0.0004708431,0.000051795043,0.0000480368,0.00016382345,0.000053513035],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0017455915,0.00077957957,0.0020045864,0.0018669972,0.0003014587,0.0013172125,0.0016341623,0.0013170951,0.0021535319],"category_scores_gemma":[0.0019075068,0.00033376177,0.00043418017,0.0019380398,0.0019374405,0.0030691482,0.0009748492,0.0021819833,0.0015551264],"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":[0.00008595805,0.000024268205,0.00059243664,0.008459997,0.00010854784,0.0008034453,0.00024060515,0.0005896766,0.0031469432,0.023280988,0.020521851,0.9421453],"study_design_scores_gemma":[0.00001713513,0.00006958928,0.0023320862,0.002131983,0.00009259896,0.0029171146,0.00020480558,0.000095043724,0.0012510662,0.02293742,0.96792233,0.000028871515],"about_ca_topic_score_codex":0.0013831359,"about_ca_topic_score_gemma":0.0016611433,"teacher_disagreement_score":0.0021535319,"about_ca_system_score_codex":0.0012046123,"about_ca_system_score_gemma":0.00096723984,"threshold_uncertainty_score":0.009231687},"labels":[],"label_agreement":null},{"id":"W2061999591","doi":"10.1016/j.jpeds.2013.03.058","title":"Thyroid Function from Birth to Adolescence in Prader-Willi Syndrome","year":2013,"lang":"en","type":"article","venue":"The Journal of Pediatrics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":53,"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; BC Children's Hospital; University of British Columbia","funders":"","keywords":"Medicine; Internal medicine; Endocrinology; Triiodothyronine; Thyroid function; Hormone; Thyroid-stimulating hormone; Thyroid; Congenital hypothyroidism; Free thyroxine; Reference range","score_opus":0.006844456755075083,"score_gpt":0.20790392653583603,"score_spread":0.20105946978076095,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2061999591","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99811435,0.0008420878,0.00007821582,0.00007175427,0.000011993468,0.0000028669588,0.0001220793,0.000009585263,0.0007470811],"genre_scores_gemma":[0.998978,0.00049720716,0.000049208775,0.000020642143,0.000008427585,0.00000389851,0.00012272283,0.0000067004617,0.000313226],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99983084,0.0000444696,0.000012644342,0.000027447635,0.000034293284,0.000050287254],"domain_scores_gemma":[0.9992737,0.00031943194,0.00012934644,0.000033373042,0.00010957167,0.00013454507],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00030279264,0.00018524447,0.00038926027,0.00093679095,0.00034040178,0.0005483786,0.00027430843,0.00038457336,0.00063704397],"category_scores_gemma":[0.002262033,0.00018646705,0.0002519846,0.0005412638,0.00031738685,0.00030745802,0.00039594734,0.00054714776,0.00015828009],"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":[0.0014239813,0.00025035208,0.94430333,0.00005393655,0.00006109078,0.0073583624,0.0016026498,0.00037161386,0.022260815,0.0002262884,0.00032443897,0.021763148],"study_design_scores_gemma":[0.0000064994074,0.00017884829,0.9932712,0.00001402063,0.000051581057,0.0029439388,0.00028922918,0.00015896784,0.0022846747,0.000078436664,0.00071367394,0.000008876472],"about_ca_topic_score_codex":0.008341259,"about_ca_topic_score_gemma":0.0059712264,"teacher_disagreement_score":0.008341259,"about_ca_system_score_codex":0.0004880874,"about_ca_system_score_gemma":0.0005209223,"threshold_uncertainty_score":0.01658541},"labels":[],"label_agreement":null},{"id":"W2062755230","doi":"10.1371/journal.pgen.1004265","title":"Parent-of-Origin Effects Implicate Epigenetic Regulation of Experimental Autoimmune Encephalomyelitis and Identify Imprinted Dlk1 as a Novel Risk Gene","year":2014,"lang":"en","type":"article","venue":"PLoS Genetics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":18,"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; Vetenskapsrådet; Multiple Sclerosis Society; Multiple Sclerosis Society of Canada; Wellcome Trust","keywords":"Biology; Epigenetics; Genetics; Genomic imprinting; Imprinting (psychology); Allele; Experimental autoimmune encephalomyelitis; Locus (genetics); Disease; Immunology; Gene; Immune system; DNA methylation; Gene expression; Medicine","score_opus":0.012785828114457524,"score_gpt":0.26633892611671917,"score_spread":0.25355309800226167,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2062755230","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99415755,0.00057040236,0.0045907754,0.000038479182,0.000006793592,0.000008790934,0.00017634411,0.00003822706,0.00041260885],"genre_scores_gemma":[0.99661106,0.00037669385,0.0021377124,0.000024805428,0.00000847752,0.000007318052,0.00016797236,0.000018374225,0.0006475575],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9996846,0.00006882383,0.000022702274,0.00010042404,0.0000893229,0.0000341138],"domain_scores_gemma":[0.9994592,0.00013486618,0.00023391203,0.00007457258,0.000035367608,0.00006207617],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00033341607,0.00045428926,0.00024128915,0.0004325356,0.000099754376,0.00022001924,0.0001731118,0.0001772489,0.0012756804],"category_scores_gemma":[0.000318376,0.00012420748,0.00021139803,0.0002066994,0.00024797392,0.00015773288,0.00029460862,0.0004822823,0.00020276044],"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":[0.0003201473,0.00003928271,0.018143054,0.000027875463,0.000032834545,0.00016255466,0.00003681341,0.00008466442,0.97620434,0.00015826509,0.000016938115,0.0047732526],"study_design_scores_gemma":[0.000032678254,0.00081848254,0.44223604,0.000017775672,0.00024392754,0.0024125213,0.00009361107,0.002686797,0.5494302,0.00036892813,0.0016415901,0.000017473601],"about_ca_topic_score_codex":0.00024623354,"about_ca_topic_score_gemma":0.00052381336,"teacher_disagreement_score":0.0012756804,"about_ca_system_score_codex":0.00016455125,"about_ca_system_score_gemma":0.0001342183,"threshold_uncertainty_score":0.0042675734},"labels":[],"label_agreement":null},{"id":"W2063012163","doi":"10.1007/s00335-002-2244-x","title":"Alternative splicing and imprinting control of the Meg3/Gtl2-Dlk1 locus in mouse embryos","year":2003,"lang":"en","type":"article","venue":"Mammalian Genome","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":32,"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","funders":"National Center for Research Resources; National Cancer Institute; Canadian Institutes of Health Research","keywords":"Genomic imprinting; Biology; MEG3; Locus (genetics); Imprinting (psychology); Genetics; Gene; Exon; Uniparental disomy; Allele; RNA splicing; Gene expression; Molecular biology; Chromosome; RNA; DNA methylation; Long non-coding RNA","score_opus":0.006323893910373239,"score_gpt":0.2093807934480102,"score_spread":0.20305689953763695,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2063012163","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.98644036,0.0018665305,0.0068352018,0.00014393646,0.000024875859,0.000013423782,0.0006800831,0.00020775392,0.003787726],"genre_scores_gemma":[0.99090815,0.0004985381,0.0027559828,0.000063122025,0.000008029282,0.000016288577,0.00053714076,0.00010990224,0.0051029464],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99984515,0.000022928612,0.00001603381,0.000040285126,0.000045925695,0.000029608624],"domain_scores_gemma":[0.9998443,0.00003081927,0.000054476728,0.00002539494,0.000016356444,0.000028672144],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00016919557,0.00024866714,0.00019642411,0.0005948789,0.0002364192,0.00053612865,0.00037496234,0.00036954347,0.0011233023],"category_scores_gemma":[0.00016904187,0.0003119073,0.00022854067,0.00021985757,0.00041483543,0.00030119528,0.00034204146,0.0005411862,0.000526242],"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":[0.00007761086,0.0000036173362,0.00041363906,0.000009881371,0.0000032992557,0.00018364421,0.00002704485,0.000081930804,0.99739337,0.00094536936,0.000030024468,0.0008304455],"study_design_scores_gemma":[0.000022276154,0.000031519416,0.011169836,0.0000071267204,0.000015206932,0.0006702572,0.000045773177,0.00066738756,0.9837986,0.00045755284,0.0031069529,0.000007410122],"about_ca_topic_score_codex":0.0015843004,"about_ca_topic_score_gemma":0.0026461808,"teacher_disagreement_score":0.0015843004,"about_ca_system_score_codex":0.0006491863,"about_ca_system_score_gemma":0.000216946,"threshold_uncertainty_score":0.0047101974},"labels":[],"label_agreement":null},{"id":"W2063715238","doi":"10.1210/endo.143.4.8746","title":"Localization and Regulation of a Functional GHRH Receptor in the Rat Renal Medulla","year":2002,"lang":"en","type":"article","venue":"Endocrinology","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":10,"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; Hôpital Notre-Dame","funders":"","keywords":"Endocrinology; Internal medicine; Internalization; Receptor; Growth hormone–releasing hormone; Biology; In situ hybridization; Riboprobe; Angiotensin II; Messenger RNA; Hormone; Chemistry; Growth hormone; Biochemistry; Medicine","score_opus":0.015360612477738622,"score_gpt":0.21797610340465154,"score_spread":0.20261549092691292,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2063715238","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.98885494,0.0055520614,0.0038490845,0.00007556951,0.000023799443,0.000015620519,0.000256717,0.00009519414,0.0012769887],"genre_scores_gemma":[0.9914779,0.0016224677,0.003603313,0.00003928098,0.000027000384,0.000030868534,0.00043651508,0.000033188117,0.0027294594],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99982363,0.000018273999,0.000015215978,0.000049201273,0.000045727957,0.000047951195],"domain_scores_gemma":[0.99972624,0.00003175498,0.000066848464,0.000033636836,0.0000557784,0.000085698375],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00020181401,0.00018415961,0.00035047234,0.00028824675,0.00014882741,0.00035892683,0.00029878682,0.00021543322,0.0007602905],"category_scores_gemma":[0.00022189297,0.00021555774,0.00041235896,0.000099153105,0.00029269062,0.00033372358,0.00023540479,0.00033046483,0.0004088567],"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":[0.00005598507,0.0000042217794,0.00016900513,0.000021971142,0.0000019624804,0.00002677017,0.000012432236,0.000014566685,0.999241,0.000051186795,0.0000063240686,0.00039472902],"study_design_scores_gemma":[0.000019863794,0.0005704149,0.053263623,0.000015462681,0.000043557946,0.0008035801,0.00013248321,0.0009342856,0.9413167,0.00010777446,0.0027769315,0.000015282318],"about_ca_topic_score_codex":0.0013843457,"about_ca_topic_score_gemma":0.0013674697,"teacher_disagreement_score":0.0013843457,"about_ca_system_score_codex":0.00033899417,"about_ca_system_score_gemma":0.00038155247,"threshold_uncertainty_score":0.0027525425},"labels":[],"label_agreement":null},{"id":"W2064431299","doi":"10.1016/j.ygeno.2004.03.008","title":"The KCNQ1OT1 promoter, a key regulator of genomic imprinting in human chromosome 11p15.5","year":2004,"lang":"en","type":"article","venue":"Genomics","topic":"Genetic Syndromes and Imprinting","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":"SickKids Foundation; Hospital for Sick Children; University of Toronto","funders":"Canadian Institutes of Health Research","keywords":"Biology; Genomic imprinting; Regulator; Imprinting (psychology); Genetics; Key (lock); Chromosome; Gene; Computational biology; DNA methylation; Gene expression","score_opus":0.0076892163561273486,"score_gpt":0.2260845621412258,"score_spread":0.21839534578509845,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2064431299","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9756605,0.0056682006,0.011686941,0.00061778235,0.00020218137,0.000052763746,0.0021622214,0.00023222956,0.003717332],"genre_scores_gemma":[0.99290484,0.00067607395,0.0023520438,0.00012452436,0.000025598652,0.000019626475,0.0013939093,0.000036469486,0.0024669843],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9998567,0.000012234391,0.0000081718945,0.000054454133,0.000042474207,0.00002594196],"domain_scores_gemma":[0.9997706,0.000051466912,0.00006930301,0.000011618368,0.0000300154,0.00006703645],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00013556072,0.0003578598,0.00023401753,0.00033768924,0.0002291774,0.00029560798,0.00031307156,0.0002795151,0.0014693325],"category_scores_gemma":[0.00040019787,0.00016029159,0.00014200903,0.0001928355,0.00047849724,0.00015828235,0.00032816353,0.00034879643,0.00053602626],"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":[0.00067962473,0.000016027578,0.009463222,0.00022864433,0.00001587509,0.0015811012,0.00015809482,0.00070273946,0.9712828,0.0014981818,0.00065565354,0.013718093],"study_design_scores_gemma":[0.00017890721,0.0003324039,0.19120099,0.00016012322,0.000089499736,0.01051949,0.00031183264,0.0034316413,0.76152927,0.002469566,0.029727893,0.000048325335],"about_ca_topic_score_codex":0.0033998017,"about_ca_topic_score_gemma":0.00428766,"teacher_disagreement_score":0.0033998017,"about_ca_system_score_codex":0.0006070099,"about_ca_system_score_gemma":0.00045650106,"threshold_uncertainty_score":0.006760001},"labels":[],"label_agreement":null},{"id":"W2066684435","doi":"10.1371/journal.pone.0097535","title":"Epigenetic Characterization of the Growth Hormone Gene Identifies SmcHD1 as a Regulator of Autosomal Gene Clusters","year":2014,"lang":"en","type":"article","venue":"PLoS ONE","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","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":"Simon Fraser University","funders":"University of California, San Diego","keywords":"Biology; DNA methylation; Epigenetics; Promoter; Gene; Genomic imprinting; Gene cluster; Genetics; Regulation of gene expression; Gene expression; Methylation; Enhancer; Locus control region; Molecular biology","score_opus":0.010552217995584241,"score_gpt":0.1889003701747626,"score_spread":0.17834815217917838,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2066684435","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99534106,0.0010173062,0.0022842493,0.00003966876,0.000010478936,0.000007104028,0.0005095234,0.00003768194,0.0007529086],"genre_scores_gemma":[0.99420303,0.0003768769,0.0018585717,0.000032673648,0.000007920132,0.000010255445,0.00095117354,0.000011407437,0.0025481111],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99995244,0.0000037259,0.0000019992017,0.000018558198,0.000015079667,0.000008136273],"domain_scores_gemma":[0.99994564,0.000010297776,0.000018126602,0.000005177484,0.0000070635933,0.0000137243405],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.000048242247,0.00012462793,0.0000942678,0.00019279875,0.00010680086,0.00010422973,0.00010018956,0.00009721964,0.0010422157],"category_scores_gemma":[0.0000816941,0.00007839931,0.00012257951,0.00012160275,0.000084023915,0.000053321077,0.00012236334,0.00019979084,0.00018735763],"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":[0.00003916235,0.000004214085,0.0018303511,0.00001960443,0.000004542126,0.00004174249,0.000016219878,0.00003697873,0.99600935,0.000065631335,0.000025874171,0.0019063959],"study_design_scores_gemma":[0.000010990485,0.00015182245,0.30964664,0.000010540676,0.000037922793,0.00048540204,0.000054304335,0.0026855676,0.6811369,0.00014473507,0.0056283493,0.000006939502],"about_ca_topic_score_codex":0.00079295307,"about_ca_topic_score_gemma":0.0019126814,"teacher_disagreement_score":0.0010422157,"about_ca_system_score_codex":0.00017574457,"about_ca_system_score_gemma":0.00010297321,"threshold_uncertainty_score":0.0034865737},"labels":[],"label_agreement":null},{"id":"W2068519968","doi":"10.1016/s1499-2671(11)52031-3","title":"Unique metabolic profile in children with Prader-Willi Syndrome: Heightened insulin sensitivity relative to body mass index","year":2011,"lang":"en","type":"article","venue":"Canadian Journal of Diabetes","topic":"Genetic Syndromes and Imprinting","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":true,"route_about_ca":false,"ca_institutions":"University of Alberta","funders":"","keywords":"Medicine; Adiponectin; Body mass index; Internal medicine; Endocrinology; Obesity; Lean body mass; Insulin sensitivity; Insulin; Fat mass; Insulin resistance; Body weight","score_opus":0.007171056441082646,"score_gpt":0.1898451893152519,"score_spread":0.18267413287416925,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2068519968","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9986248,0.00021944917,0.000109327506,0.00009656265,0.000016215716,0.0000059536583,0.00021477613,0.000015062489,0.0006978804],"genre_scores_gemma":[0.99926406,0.00016140233,0.00020627752,0.000039497816,0.000024499739,0.000006098706,0.00017465955,0.000007621071,0.000115841925],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9996724,0.000054015767,0.000036625104,0.00007744179,0.000092464266,0.000067096254],"domain_scores_gemma":[0.9993358,0.00014500435,0.00023415589,0.000031928535,0.0000419253,0.00021104288],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00020958453,0.0007547562,0.0005795985,0.0014334727,0.00044432151,0.0005902149,0.00038920014,0.0005260585,0.0013409525],"category_scores_gemma":[0.0016539415,0.00029277796,0.00033823663,0.0011730504,0.00045616174,0.0003183918,0.0005512943,0.00086852326,0.00017057698],"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":[0.00038130974,0.000074195355,0.9659456,0.000024521132,0.000052138123,0.022088446,0.00035396116,0.00012275811,0.007519226,0.00014460164,0.00017274478,0.003120435],"study_design_scores_gemma":[0.000008477892,0.00020150341,0.95845896,0.000007855378,0.000043272168,0.039886884,0.0004671153,0.00016277847,0.00048415226,0.00009356911,0.00017446303,0.000011091072],"about_ca_topic_score_codex":0.003582603,"about_ca_topic_score_gemma":0.0035678705,"teacher_disagreement_score":0.003582603,"about_ca_system_score_codex":0.00030271988,"about_ca_system_score_gemma":0.00035045095,"threshold_uncertainty_score":0.0071234703},"labels":[],"label_agreement":null},{"id":"W2068741665","doi":"10.1002/dvdy.21615","title":"Loss of the Prader‐Willi syndrome protein necdin causes defective migration, axonal outgrowth, and survival of embryonic sympathetic neurons","year":2008,"lang":"en","type":"article","venue":"Developmental Dynamics","topic":"Genetic Syndromes and Imprinting","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 Alberta","funders":"Fondation pour la Recherche Médicale","keywords":"Biology; Superior cervical ganglion; Endocrinology; Sympathetic nervous system; Internal medicine; Embryonic stem cell; Nervous system; Neuroscience; Medicine","score_opus":0.008480482013126636,"score_gpt":0.2012182157645916,"score_spread":0.19273773375146497,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2068741665","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9987496,0.00015028192,0.0005907699,0.000019930916,0.0000052146547,0.000003892826,0.00008222998,0.000018738941,0.00037924325],"genre_scores_gemma":[0.9971028,0.0002832779,0.0011704359,0.00001115021,0.0000023932205,0.000011066868,0.0001666816,0.000015826758,0.0012364731],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9998404,0.000028765862,0.000025610861,0.00003056208,0.000052160227,0.000022469034],"domain_scores_gemma":[0.9998056,0.000055136097,0.00005867293,0.000026598074,0.000008645166,0.00004533581],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00009518301,0.0003320264,0.00015348158,0.00030638883,0.00012009089,0.00013706117,0.00021614038,0.00024354707,0.0008702708],"category_scores_gemma":[0.00029765637,0.00023585297,0.00015878785,0.0001116269,0.00035010334,0.00011797723,0.0003943449,0.00037961392,0.000213972],"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":[0.00010970094,0.000022288395,0.0014021681,0.00002342648,0.000011672422,0.0014223631,0.000034565583,0.00030387976,0.99440104,0.00020671106,0.00004561121,0.0020166175],"study_design_scores_gemma":[0.00007011527,0.0005796626,0.058925726,0.000022403561,0.000066653534,0.013301056,0.00010438649,0.0044800094,0.9187257,0.00028711668,0.0034131524,0.000023930257],"about_ca_topic_score_codex":0.0010290336,"about_ca_topic_score_gemma":0.0016950736,"teacher_disagreement_score":0.0010290336,"about_ca_system_score_codex":0.0002173661,"about_ca_system_score_gemma":0.00021576439,"threshold_uncertainty_score":0.0029113293},"labels":[],"label_agreement":null},{"id":"W2069432272","doi":"10.1002/dvg.20658","title":"Loss of Necdin impairs myosin activation and delays cell polarization","year":2010,"lang":"en","type":"article","venue":"genesis","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":16,"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 Institute of General Medical Sciences; RIKEN; Canadian Institutes of Health Research; Heritage Medical Research Institute","keywords":"Cell polarity; Myosin; Cell biology; Biology; Null cell; PAX3; Neuroscience; Cell; Genetics; Cell culture; Gene; Transcription factor","score_opus":0.0046401020041517615,"score_gpt":0.20715645552047163,"score_spread":0.20251635351631986,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2069432272","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9975987,0.0002864904,0.00076036126,0.000041885087,0.000009603087,0.000003828882,0.00013778168,0.000028473669,0.0011328661],"genre_scores_gemma":[0.99616647,0.00029667455,0.0006378404,0.000018506898,0.0000017544207,0.000008571057,0.00025301176,0.000011719536,0.0026054617],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9999105,0.000012589445,0.0000125732695,0.000017425951,0.00002762119,0.000019363451],"domain_scores_gemma":[0.9998939,0.000023536122,0.000026178035,0.000014759801,0.0000072813805,0.00003432565],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00006253058,0.000259054,0.00011346244,0.00016335439,0.00009030648,0.00017434474,0.00014791194,0.0001831955,0.0012880579],"category_scores_gemma":[0.00011644891,0.00014231211,0.00010557727,0.00008382736,0.00020272796,0.00012468832,0.00024725337,0.0003243363,0.00035328232],"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":[0.000044063832,0.000007940416,0.00014057836,0.0000105159825,0.000001825392,0.00007782221,0.0000063393454,0.00003306756,0.9989704,0.000066997236,0.000014326458,0.0006261542],"study_design_scores_gemma":[0.0000127518715,0.00014601903,0.0067787073,0.000004778337,0.000008837193,0.00066458486,0.000022634305,0.0008427219,0.989945,0.000058887013,0.001512503,0.0000025826998],"about_ca_topic_score_codex":0.0007067568,"about_ca_topic_score_gemma":0.0013293815,"teacher_disagreement_score":0.0012880579,"about_ca_system_score_codex":0.0002419448,"about_ca_system_score_gemma":0.00016268335,"threshold_uncertainty_score":0.0043089986},"labels":[],"label_agreement":null},{"id":"W2069564940","doi":"10.1053/plac.2001.0695","title":"The Human Achaete Scute Homolog 2 Gene Contains Two Promotors, Generating Overlapping Transcripts and Encoding Two Proteins with Different Nuclear Localization","year":2001,"lang":"en","type":"article","venue":"Placenta","topic":"Genetic Syndromes and Imprinting","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":"Institute of Genetics; University of Cambridge","keywords":"Biology; Gene; Molecular biology; Gene expression; Homology (biology); Transcription (linguistics); Coding region; Messenger RNA; Fusion protein; Nucleolus; Nuclear protein; Genetics; Transcription factor; Nucleus; Cell biology; Recombinant DNA","score_opus":0.011833631285774544,"score_gpt":0.23662429757765885,"score_spread":0.2247906662918843,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2069564940","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9779178,0.0018703851,0.014336755,0.00023519731,0.00007229717,0.000054734548,0.00075596664,0.0002471237,0.0045097503],"genre_scores_gemma":[0.98059124,0.0006527515,0.00597879,0.000090899215,0.000048081394,0.000051572297,0.0021621727,0.00006479488,0.0103598125],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9998192,0.00002054251,0.000008465901,0.00004844686,0.000061929095,0.00004142615],"domain_scores_gemma":[0.99953806,0.00017245053,0.000069120906,0.000060046354,0.00004208093,0.00011830725],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00013911896,0.0007086256,0.0003913133,0.0010110443,0.0005449942,0.000546916,0.00036079946,0.0005589843,0.0019571176],"category_scores_gemma":[0.0003477603,0.00043674762,0.0005579484,0.0005496146,0.0008682726,0.0002940272,0.00062958186,0.00083694514,0.0008175304],"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":[0.00028753243,0.000030634048,0.00194627,0.000056414432,0.000016954198,0.0007996176,0.00013097073,0.00011773699,0.98957,0.0016180411,0.00010818124,0.0053175604],"study_design_scores_gemma":[0.00010978367,0.00029047765,0.050597593,0.00003016268,0.000091230584,0.006542471,0.00031235037,0.0011819573,0.92256725,0.0013567106,0.016882177,0.00003779011],"about_ca_topic_score_codex":0.0013281445,"about_ca_topic_score_gemma":0.0018085007,"teacher_disagreement_score":0.0019571176,"about_ca_system_score_codex":0.0004177054,"about_ca_system_score_gemma":0.00050208875,"threshold_uncertainty_score":0.0065472126},"labels":[],"label_agreement":null},{"id":"W2069928748","doi":"10.1210/jc.2004-0553","title":"The<i>Insulin-Like Growth Factor-II Receptor</i>Gene Is Associated with Type 1 Diabetes: Evidence of a Maternal Effect","year":2004,"lang":"en","type":"article","venue":"The Journal of Clinical Endocrinology & Metabolism","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":26,"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 Children's Hospital","funders":"","keywords":"Insulin-like growth factor 2 receptor; Single-nucleotide polymorphism; Biology; Genomic imprinting; Linkage disequilibrium; Allele; Genetics; SNP; Imprinting (psychology); Haplotype; Gene; Genotype; Receptor; DNA methylation; Insulin-like growth factor 1 receptor; Gene expression; Growth factor","score_opus":0.025050048350509002,"score_gpt":0.31311042205817785,"score_spread":0.28806037370766885,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2069928748","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9957865,0.0014276602,0.0012461368,0.00016900539,0.000029991568,0.0000057184147,0.000446989,0.000039117607,0.0008488507],"genre_scores_gemma":[0.99598724,0.0008586756,0.0015575505,0.00012891907,0.000078016084,0.000010814817,0.0005910865,0.000025057587,0.0007626516],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99974376,0.00005708897,0.000026308919,0.00010400706,0.00004869648,0.000020024676],"domain_scores_gemma":[0.999554,0.00010957899,0.0002065549,0.000050478706,0.000024501052,0.000054932614],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00021220985,0.00044961472,0.00021369634,0.00054214,0.00019459926,0.0003035097,0.0003163458,0.00041297346,0.003224467],"category_scores_gemma":[0.00060626114,0.00017138629,0.00032343832,0.0005516215,0.00026196643,0.00012450677,0.00021514973,0.00041360737,0.0004232789],"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":[0.0054872534,0.00016980726,0.55607647,0.00021607809,0.0007509018,0.004608659,0.00022678795,0.00025116105,0.40737832,0.00037038044,0.0009776803,0.023486545],"study_design_scores_gemma":[0.00012749857,0.00044399253,0.96766406,0.000031673015,0.0005043215,0.009360454,0.00005886959,0.0008364304,0.01820395,0.0001881656,0.0025651965,0.000015466609],"about_ca_topic_score_codex":0.0010331391,"about_ca_topic_score_gemma":0.0008110073,"teacher_disagreement_score":0.003224467,"about_ca_system_score_codex":0.0001515454,"about_ca_system_score_gemma":0.00011179596,"threshold_uncertainty_score":0.010786891},"labels":[],"label_agreement":null},{"id":"W2070045006","doi":"10.1002/jcb.20365","title":"Chromatin modification of the human imprinted <i>NDN</i> (necdin) gene detected by in vivo footprinting","year":2005,"lang":"en","type":"article","venue":"Journal of Cellular Biochemistry","topic":"Genetic Syndromes and Imprinting","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":"Université de Sherbrooke; University of Alberta","funders":"Eunice Kennedy Shriver National Institute of Child Health and Human Development","keywords":"Genomic imprinting; Chromatin; Epigenetics; Biology; Gene; Allele; Footprinting; Genetics; Imprinting (psychology); DNA methylation; Transcription (linguistics); Chromosome conformation capture; Molecular biology; Transcription factor; Gene expression; Enhancer","score_opus":0.006626311671510045,"score_gpt":0.22549247214543974,"score_spread":0.2188661604739297,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2070045006","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9890617,0.00064257253,0.008565984,0.000046908095,0.000016035989,0.000010511244,0.00024572414,0.00006755145,0.0013430272],"genre_scores_gemma":[0.99443805,0.00024823265,0.0037355402,0.000020455538,0.000003164871,0.000008168107,0.00035407883,0.000013211094,0.001179019],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9999329,0.00001221428,0.000003681928,0.00002662395,0.000016144513,0.000008505874],"domain_scores_gemma":[0.9998852,0.00004088816,0.000027547521,0.00002057296,0.000007442794,0.000018354316],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.000077881945,0.00017884694,0.000088352695,0.00010514043,0.00007861109,0.0001602427,0.00012436663,0.00012959227,0.0013445703],"category_scores_gemma":[0.00013129957,0.000104027764,0.00012321984,0.00008448155,0.00020089324,0.00009184252,0.000118941556,0.00021200863,0.00027256593],"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":[0.000026590604,0.000003602053,0.0003492695,0.000010263291,0.0000026994783,0.000031378782,0.000008874737,0.000028828423,0.99873394,0.00003947611,0.000006689255,0.00075842475],"study_design_scores_gemma":[0.000004304093,0.0000526378,0.014221414,0.000002279506,0.0000067362307,0.0002620962,0.0000125995875,0.0005068079,0.98393005,0.00004476157,0.000954232,0.0000020615903],"about_ca_topic_score_codex":0.0007857105,"about_ca_topic_score_gemma":0.001359243,"teacher_disagreement_score":0.0013445703,"about_ca_system_score_codex":0.00023503273,"about_ca_system_score_gemma":0.00007570864,"threshold_uncertainty_score":0.004498005},"labels":[],"label_agreement":null},{"id":"W2070502226","doi":"10.1371/journal.pgen.0030065","title":"Identification of the Imprinted KLF14 Transcription Factor Undergoing Human-Specific Accelerated Evolution","year":2007,"lang":"en","type":"article","venue":"PLoS Genetics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":114,"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":"Natural Sciences and Engineering Research Council of Canada; National Institutes of Health; Canadian Institutes of Health Research; Genome Canada; Ontario Genomics; Wellcome Trust; National Center for Research Resources; Ontario Genomics Institute; Howard Hughes Medical Institute","keywords":"Biology; Genomic imprinting; Genetics; Epigenomics; DNA methylation; Epigenetics; CpG site; Human genome; Chromatin immunoprecipitation; Gene; Gene expression; Genome; Promoter","score_opus":0.03302141642389157,"score_gpt":0.26380843551479244,"score_spread":0.23078701909090088,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2070502226","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99696964,0.00043413724,0.0018641212,0.000017927652,0.0000039476095,0.000005858039,0.00026008557,0.00002444437,0.00041988073],"genre_scores_gemma":[0.9952663,0.00028951152,0.002548738,0.000038068323,0.000008913662,0.0000079288975,0.00084321504,0.000010270468,0.0009871504],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9999455,0.0000073851925,0.0000033759807,0.00001985571,0.000014403874,0.0000094642],"domain_scores_gemma":[0.99989474,0.000016763639,0.000040240586,0.000012633265,0.000013865826,0.000021774455],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.000093266535,0.00010283859,0.00012883416,0.0002991876,0.000097644144,0.00012519883,0.00012910791,0.0001365605,0.00059013587],"category_scores_gemma":[0.00016508796,0.00007683291,0.00012178179,0.00016619782,0.00009192576,0.00007460637,0.00013721104,0.00012721881,0.00019929386],"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":[0.00019498891,0.000014838423,0.04518401,0.000037104,0.000033053333,0.0002873182,0.000059364054,0.0001929515,0.9394045,0.0002913873,0.00008400985,0.01421655],"study_design_scores_gemma":[0.0000183692,0.00043160256,0.73786134,0.000016952996,0.00006439006,0.0036260954,0.00008265639,0.0030987253,0.24709465,0.00031901314,0.007366171,0.0000199741],"about_ca_topic_score_codex":0.0004991983,"about_ca_topic_score_gemma":0.00094185246,"teacher_disagreement_score":0.00059013587,"about_ca_system_score_codex":0.00012944678,"about_ca_system_score_gemma":0.00011430165,"threshold_uncertainty_score":0.001974225},"labels":[],"label_agreement":null},{"id":"W2070677464","doi":"10.1182/blood-2009-03-212746","title":"An upstream insulator regulates DLK1 imprinting in AML","year":2010,"lang":"en","type":"article","venue":"Blood","topic":"Genetic Syndromes and Imprinting","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":"University of Toronto; Ontario Institute for Cancer Research","funders":"","keywords":"Genomic imprinting; Biology; Methylation; Imprinting (psychology); Molecular biology; Allele; Epigenetics; DNA methylation; Myeloid leukemia; Uniparental disomy; Cancer research; Genetics; Gene; Gene expression; Chromosome","score_opus":0.004282711526569268,"score_gpt":0.22481929011371826,"score_spread":0.220536578587149,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2070677464","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9971131,0.00050829817,0.0012697432,0.00005877566,0.0000075811035,0.000004163264,0.00011482359,0.00008822573,0.00083526224],"genre_scores_gemma":[0.99864525,0.00014338255,0.00051934324,0.000017731683,0.0000035126968,0.0000022526133,0.00010774977,0.000011008098,0.0005496119],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9999404,0.000007321857,0.000003227671,0.000012614025,0.000017821805,0.00001862043],"domain_scores_gemma":[0.9999037,0.00001917072,0.00003201084,0.000008651558,0.000005699427,0.00003070003],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00006002584,0.0001304481,0.00010357818,0.0002511451,0.00010029088,0.00015861564,0.00009825987,0.00009060864,0.001183853],"category_scores_gemma":[0.0001859167,0.000098413846,0.00007052915,0.000112091526,0.00017924182,0.00008525426,0.00020232843,0.0002209931,0.00028887484],"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":[0.000105861975,0.000007567292,0.003889577,0.000011246387,0.0000021906114,0.00014062937,0.000020939662,0.00004501675,0.9926025,0.00018941032,0.000046216326,0.0029386817],"study_design_scores_gemma":[0.000044430737,0.00018328354,0.22280619,0.000010461877,0.000037056205,0.0023314948,0.00007829791,0.0019591062,0.7679537,0.00062335865,0.003962305,0.000010374335],"about_ca_topic_score_codex":0.00041743633,"about_ca_topic_score_gemma":0.0007741105,"teacher_disagreement_score":0.001183853,"about_ca_system_score_codex":0.00024479162,"about_ca_system_score_gemma":0.00012474872,"threshold_uncertainty_score":0.0039604306},"labels":[],"label_agreement":null},{"id":"W2071121505","doi":"10.1097/00019605-200404000-00008","title":"Severe hemihypotrophy in a female infant with mosaic Turner syndrome: a variant of Russell???Silver syndrome?","year":2004,"lang":"en","type":"article","venue":"Clinical Dysmorphology","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":14,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Health Sciences Centre; University of Manitoba","funders":"","keywords":"Medicine; Failure to thrive; Uniparental disomy; Karyotype; Forehead; Dermatology; Anatomy; Pediatrics; Genetics; Chromosome; Biology","score_opus":0.015443451725337043,"score_gpt":0.2720193214719298,"score_spread":0.25657586974659274,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2071121505","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99531955,0.00058239157,0.00080179796,0.00047280168,0.00005696869,0.000032763786,0.00008977754,0.00008406021,0.002559846],"genre_scores_gemma":[0.9984786,0.00029140757,0.00041662465,0.00010473398,0.00008000818,0.0000093476565,0.000032113443,0.000013692186,0.0005735223],"study_design_codex":"case_report","study_design_gemma":"case_report","domain_scores_codex":[0.99971837,0.000036605412,0.000018748568,0.00007210664,0.00007820729,0.000076017204],"domain_scores_gemma":[0.9996847,0.00007665687,0.000092294926,0.000018177085,0.00001167508,0.00011659197],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00024152045,0.0009838027,0.0005236923,0.0007572478,0.0006124723,0.00042742217,0.0003347991,0.0012330561,0.0012641101],"category_scores_gemma":[0.0013869903,0.00049475196,0.00033585023,0.0003550422,0.0009310082,0.00039645878,0.0006604254,0.0009331586,0.00018819554],"study_design_candidate":"case_report","study_design_consensus":"case_report","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00010606992,0.000020919759,0.013870681,0.000034007127,0.000014595016,0.97243124,0.0002615974,0.00009659131,0.009958069,0.00035503405,0.00018576834,0.002665427],"study_design_scores_gemma":[0.000018836985,0.00018676968,0.023742113,0.00000856329,0.000018247683,0.97362816,0.0000770666,0.00021710069,0.0015596309,0.00015128618,0.00038137476,0.000010797444],"about_ca_topic_score_codex":0.0018174993,"about_ca_topic_score_gemma":0.0026258505,"teacher_disagreement_score":0.0018174993,"about_ca_system_score_codex":0.00047460425,"about_ca_system_score_gemma":0.000374824,"threshold_uncertainty_score":0.0042288303},"labels":[],"label_agreement":null},{"id":"W2071975392","doi":"10.1210/jcem.86.10.7940","title":"Gαs Transcripts Are Biallelically Expressed in the Human Kidney Cortex: Implications for Pseudohypoparathyroidism Type 1b","year":2001,"lang":"en","type":"article","venue":"The Journal of Clinical Endocrinology & Metabolism","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":50,"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":"Pseudohypoparathyroidism; GNAS complex locus; Internal medicine; Endocrinology; Biology; Genomic imprinting; Locus (genetics); Exon; Imprinting (psychology); Allele; Genetics; Parathyroid hormone; Gene expression; Medicine; Gene","score_opus":0.07749785752955718,"score_gpt":0.38442556502469705,"score_spread":0.30692770749513987,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2071975392","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99797493,0.0007213517,0.00051916175,0.000065636545,0.000004354117,0.000003586261,0.00015596107,0.000032268625,0.00052258477],"genre_scores_gemma":[0.99859065,0.00029232347,0.00033327416,0.000028902901,0.0000056772624,0.000003923833,0.0001848508,0.000010033323,0.0005502975],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9999058,0.000010888225,0.0000057245843,0.00003199434,0.000027340539,0.000018313554],"domain_scores_gemma":[0.99980384,0.000038105583,0.000076416734,0.000020347063,0.000016867649,0.000044458222],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00009155195,0.00017313275,0.00012503706,0.000649333,0.0002067463,0.00033715606,0.00010633067,0.00020680368,0.0015506351],"category_scores_gemma":[0.00030734754,0.00019348085,0.00012149078,0.00019942733,0.00030247757,0.000088479,0.00024291579,0.00018117642,0.00025596737],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0002373328,0.000006160495,0.012443743,0.000026864656,0.000011498129,0.0014607105,0.000096214106,0.00004243698,0.983396,0.00011232146,0.000053356278,0.0021133148],"study_design_scores_gemma":[0.000066671055,0.00022685125,0.70731056,0.000023083372,0.0001088136,0.03287438,0.00040574698,0.0008878833,0.25248492,0.0006175667,0.0049719443,0.00002158916],"about_ca_topic_score_codex":0.0010625325,"about_ca_topic_score_gemma":0.0013395133,"teacher_disagreement_score":0.0015506351,"about_ca_system_score_codex":0.00015980752,"about_ca_system_score_gemma":0.00016458391,"threshold_uncertainty_score":0.005187452},"labels":[],"label_agreement":null},{"id":"W2072627772","doi":"10.1186/1471-213x-10-50","title":"Rescue of placental phenotype in a mechanistic model of Beckwith-Wiedemann syndrome","year":2010,"lang":"en","type":"article","venue":"BMC Developmental Biology","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":11,"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 Cancer Institute; Canadian Institutes of Health Research; National Institutes of Health","keywords":"Placentation; Biology; Genomic imprinting; Genetics; Epigenetics; Gene; Phenotype; Imprinting (psychology); Gene silencing; Allele; X-inactivation; Genetic screen; Placenta; X chromosome; DNA methylation; Gene expression; Fetus","score_opus":0.014895957353840273,"score_gpt":0.24016786050549213,"score_spread":0.22527190315165185,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2072627772","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9888416,0.00166128,0.004767104,0.00024280125,0.00008423467,0.00011860168,0.0008687505,0.00034604224,0.0030695447],"genre_scores_gemma":[0.98977333,0.0016602009,0.004245055,0.000101697784,0.000019144123,0.00011603081,0.00086473126,0.0000629509,0.0031568673],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.999816,0.00003889177,0.000020407397,0.000042442152,0.00005524931,0.00002698194],"domain_scores_gemma":[0.9998166,0.000033927812,0.00005468144,0.000028174718,0.000007406584,0.000059247217],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00020306787,0.000770516,0.00035195125,0.00081550464,0.00029128868,0.00026760984,0.00031949498,0.0005882092,0.0020492822],"category_scores_gemma":[0.00016675594,0.00027583897,0.00030855156,0.00020774202,0.00045338296,0.00018382909,0.0004972277,0.0007172569,0.00040468608],"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":[0.0005195902,0.00016412338,0.0006124357,0.00013299104,0.000031812342,0.003069813,0.00006512918,0.0003630472,0.9908614,0.001143322,0.00023838309,0.0027979675],"study_design_scores_gemma":[0.0004338015,0.003973576,0.013397888,0.00011537085,0.00023901134,0.034610763,0.00023152962,0.0046852105,0.9219896,0.0012767449,0.018994551,0.000051974053],"about_ca_topic_score_codex":0.00040716206,"about_ca_topic_score_gemma":0.0006684701,"teacher_disagreement_score":0.0020492822,"about_ca_system_score_codex":0.00029775058,"about_ca_system_score_gemma":0.00029815198,"threshold_uncertainty_score":0.006855607},"labels":[],"label_agreement":null},{"id":"W2073875831","doi":"10.1002/ajmg.a.33172","title":"Pseudohypoparathyroidism type 1a and the <i>GNAS</i> p.R231H mutation: Somatic mosaicism in a mother with two affected sons","year":2010,"lang":"en","type":"article","venue":"American Journal of Medical Genetics Part A","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":19,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"BC Children's Hospital; Child and Family Research Institute; University of British Columbia","funders":"Canadian Institutes of Health Research","keywords":"GNAS complex locus; Pseudohypoparathyroidism; Mutation; Genetics; Somatic cell; Germline mutation; Biology; Endocrinology; Germline mosaicism; Internal medicine; Medicine; Parathyroid hormone; Gene","score_opus":0.004315960447831264,"score_gpt":0.25215557719935416,"score_spread":0.2478396167515229,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2073875831","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.996214,0.000348179,0.00066658965,0.000538085,0.000097629425,0.00003934933,0.000081509526,0.000034846915,0.001979813],"genre_scores_gemma":[0.9973717,0.00025004617,0.0008153766,0.00016375192,0.00010469891,0.000015921536,0.0000592337,0.000024715486,0.0011945952],"study_design_codex":"case_report","study_design_gemma":"case_report","domain_scores_codex":[0.9995696,0.00006361798,0.000050708444,0.00011916184,0.0001049836,0.000091927584],"domain_scores_gemma":[0.9990221,0.00031095603,0.0001896948,0.000055076285,0.000055890607,0.00036623643],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0002809983,0.0009445156,0.0007231351,0.0010833931,0.0009876856,0.00079172576,0.0007582201,0.0017799286,0.0017615621],"category_scores_gemma":[0.00205675,0.00075697765,0.000754831,0.00035413442,0.0008863638,0.0004396801,0.00078785815,0.0010766304,0.00067645917],"study_design_candidate":"case_report","study_design_consensus":"case_report","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00006167331,0.000058840826,0.014049308,0.000029485087,0.000018644898,0.9773088,0.00070591184,0.000057969315,0.0055484353,0.00018634651,0.00020816011,0.0017663153],"study_design_scores_gemma":[0.00002308859,0.00015449934,0.021877892,0.000012114695,0.000021302036,0.97459656,0.00020462724,0.00026799878,0.002011796,0.00010637335,0.00070727157,0.000016486483],"about_ca_topic_score_codex":0.0017348925,"about_ca_topic_score_gemma":0.0020660048,"teacher_disagreement_score":0.0017799286,"about_ca_system_score_codex":0.0007369259,"about_ca_system_score_gemma":0.00036665687,"threshold_uncertainty_score":0.005892992},"labels":[],"label_agreement":null},{"id":"W2073877274","doi":"10.1159/000078197","title":"Genetic and genomic approaches to study placental development","year":2004,"lang":"en","type":"review","venue":"Cytogenetic and Genome Research","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","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":"University of Calgary","funders":"","keywords":"Biology; Computational biology; Profiling (computer programming); Context (archaeology); Identification (biology); Genetic engineering; Gene expression profiling; Evolutionary biology; Genetics; Bioinformatics; Gene; Gene expression; Computer science","score_opus":0.25139101583879053,"score_gpt":0.373508512475132,"score_spread":0.12211749663634147,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2073877274","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":[0.00012017028,0.99353325,0.0018271971,0.00049937336,0.00042345648,0.000013864127,0.000020110565,0.000028248583,0.0035342448],"genre_scores_gemma":[0.00078150025,0.9944218,0.0022096878,0.0004161555,0.00021967478,0.00002581815,0.000038910555,0.0000048972724,0.001881552],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.99961936,0.00008127737,0.000038779872,0.00007887137,0.00015539177,0.00002636743],"domain_scores_gemma":[0.9996908,0.00014114524,0.000026295984,0.00003430418,0.00007223873,0.00003519124],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0011951096,0.001464154,0.0015059735,0.0037019309,0.0004587336,0.0011592855,0.0016621945,0.0020327005,0.0041613625],"category_scores_gemma":[0.000818449,0.0004540737,0.00062761415,0.002768171,0.0016014454,0.0018123757,0.0010934075,0.0031634397,0.0053278366],"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":[0.00007358297,0.00010734445,0.00033659753,0.009755795,0.00011664281,0.0010510135,0.00013928361,0.00087128096,0.017453294,0.031006366,0.036047872,0.903041],"study_design_scores_gemma":[0.000014649209,0.00004254595,0.0004985174,0.00095755333,0.00004311041,0.0024805027,0.000058797406,0.000061727376,0.0020694744,0.006457232,0.98729116,0.000024724513],"about_ca_topic_score_codex":0.0013420985,"about_ca_topic_score_gemma":0.0017341767,"teacher_disagreement_score":0.0041613625,"about_ca_system_score_codex":0.0013369031,"about_ca_system_score_gemma":0.0011030288,"threshold_uncertainty_score":0.013921142},"labels":[],"label_agreement":null},{"id":"W2074305055","doi":"10.1016/j.mce.2007.04.002","title":"Regulation of growth hormone expression by Delta-like protein 1 (Dlk1)","year":2007,"lang":"en","type":"article","venue":"Molecular and Cellular Endocrinology","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":40,"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; Jarislowsky Foundation; National Institute of Diabetes and Digestive and Kidney Diseases; University of Missouri","keywords":"Transcription factor; Biology; Psychological repression; Transfection; Promoter; Reporter gene; Regulation of gene expression; Epidermal growth factor; Gene; Gene expression; Molecular biology; Cell biology; Cell culture; Genetics","score_opus":0.004979355010618277,"score_gpt":0.20639719844591228,"score_spread":0.201417843435294,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2074305055","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9918561,0.0028312516,0.0023850966,0.00023408781,0.00005410719,0.000008581796,0.0004691869,0.000109007015,0.0020525525],"genre_scores_gemma":[0.99544924,0.0007098208,0.00086137926,0.000056757664,0.0000061636924,0.0000071993686,0.0004524723,0.000019852669,0.0024370325],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9999187,0.000012619444,0.0000062998397,0.000023138151,0.00001345198,0.000025776211],"domain_scores_gemma":[0.9999039,0.000019319461,0.0000339881,0.0000099607905,0.000008447955,0.000024365185],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.000092025824,0.00033611958,0.00015367474,0.00027908958,0.00015186105,0.0004152107,0.0002543484,0.00015621827,0.0009799439],"category_scores_gemma":[0.00015182846,0.0001811203,0.000121536665,0.0001289813,0.00034834427,0.00021691994,0.00037266753,0.000364839,0.00034055792],"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":[0.00023502791,0.000011094909,0.00083103095,0.000022771334,0.000003945793,0.00010404027,0.000015527354,0.00011910191,0.99638176,0.00032940807,0.00008341404,0.0018628187],"study_design_scores_gemma":[0.000035392804,0.00008175047,0.016795926,0.0000074889463,0.00001386153,0.0004460235,0.00009525186,0.0019181668,0.9772652,0.00025492665,0.0030760483,0.000009960376],"about_ca_topic_score_codex":0.00091063423,"about_ca_topic_score_gemma":0.0014633357,"teacher_disagreement_score":0.0009799439,"about_ca_system_score_codex":0.0007727539,"about_ca_system_score_gemma":0.00019637017,"threshold_uncertainty_score":0.0056067705},"labels":[],"label_agreement":null},{"id":"W2077085008","doi":"10.1210/jcem.86.3.7364","title":"Analysis of the P3 Promoter of the Human Parathyroid Hormone (PTH)/PTH-Related Peptide Receptor Gene in Pseudohypoparathyroidism Type 1b1","year":2001,"lang":"en","type":"article","venue":"The Journal of Clinical Endocrinology & Metabolism","topic":"Genetic Syndromes and Imprinting","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":"McGill University; Royal Victoria Hospital","funders":"Novo Nordisk","keywords":"Promoter; Pseudohypoparathyroidism; Gene; Parathyroid hormone; DNA methylation; Methylation; Biology; Molecular biology; Coding region; Receptor; Internal medicine; Endocrinology; Genetics; Gene expression; Medicine; Calcium","score_opus":0.0295266382144212,"score_gpt":0.32701195916770187,"score_spread":0.2974853209532807,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2077085008","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9985071,0.0002897357,0.00081830996,0.000025741492,0.0000023450093,0.0000066153643,0.00009991536,0.000013023449,0.00023726946],"genre_scores_gemma":[0.9989838,0.00012229069,0.00050692726,0.000016875896,0.0000029010607,0.000006822368,0.00017486437,0.0000068774903,0.00017859049],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99989355,0.00001962252,0.0000063557904,0.000030859024,0.000032569606,0.00001710288],"domain_scores_gemma":[0.999841,0.00007333571,0.000033507626,0.000011401102,0.000014385992,0.000026396074],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00008321926,0.00017765907,0.00012748306,0.00046384637,0.0001596109,0.00014176792,0.000117155716,0.0003198052,0.00088516535],"category_scores_gemma":[0.0004321995,0.0001381293,0.00023713599,0.00022518286,0.00018437555,0.00007283835,0.00012098213,0.0002889517,0.00024736894],"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":[0.00060320046,0.000039892908,0.08322074,0.0000695482,0.00003089501,0.0039021696,0.0004499002,0.0001912166,0.9026304,0.00009345195,0.00006744173,0.008701206],"study_design_scores_gemma":[0.00010604653,0.0008126153,0.74734133,0.000032079723,0.00010861199,0.039563257,0.00033476343,0.0023842922,0.20638071,0.0002874345,0.0026289846,0.000019815492],"about_ca_topic_score_codex":0.0012060094,"about_ca_topic_score_gemma":0.0007466951,"teacher_disagreement_score":0.0012060094,"about_ca_system_score_codex":0.00015215151,"about_ca_system_score_gemma":0.000106517,"threshold_uncertainty_score":0.0029611588},"labels":[],"label_agreement":null},{"id":"W2077235837","doi":"10.1016/j.artres.2008.08.309","title":"P1.01 TREATMENT WITH DEXAMETHASONE REVERSES IMPARED ELASTOGENESIS AND COLLAGENOGENESIS IN CULTURES OF FIBROBLASTS FROM PATIENTS WITH LOEYS-DIETZ SYNDROME (LDS)","year":2008,"lang":"en","type":"article","venue":"Artery Research","topic":"Genetic Syndromes and Imprinting","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":"Hospital for Sick Children","funders":"","keywords":"Medicine; Dexamethasone; Internal medicine","score_opus":0.027110418449368647,"score_gpt":0.2762683297107883,"score_spread":0.24915791126141965,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2077235837","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9915496,0.0033264367,0.0008529112,0.00041647014,0.0005403221,0.000039375976,0.0006258125,0.00008338574,0.0025657013],"genre_scores_gemma":[0.9933983,0.0011247613,0.0008678582,0.00010915235,0.00011388496,0.000046812118,0.000813171,0.000025386367,0.0035006986],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99955934,0.00010464985,0.000058242636,0.00008303993,0.00005927322,0.00013543187],"domain_scores_gemma":[0.99919957,0.000349513,0.000050251332,0.00010998565,0.0000485512,0.00024213684],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0002938907,0.0004395468,0.0006514535,0.0004003702,0.00034069477,0.00050161686,0.0005377695,0.00060920767,0.004995096],"category_scores_gemma":[0.00074043084,0.00021465898,0.00041125703,0.00031705748,0.0007086678,0.00027877788,0.00029777558,0.0014534635,0.00077929074],"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":[0.005232903,0.00041111183,0.0009795112,0.00011546697,0.000033121934,0.0017030487,0.00016495553,0.000057514353,0.9863219,0.00027692167,0.00033634016,0.0043671266],"study_design_scores_gemma":[0.0005937177,0.0036628346,0.013130427,0.000025781435,0.00006690513,0.0026376923,0.000451961,0.0004930334,0.9734084,0.0001589446,0.005354062,0.000016103988],"about_ca_topic_score_codex":0.002466313,"about_ca_topic_score_gemma":0.0032624002,"teacher_disagreement_score":0.004995096,"about_ca_system_score_codex":0.00023947898,"about_ca_system_score_gemma":0.00056897925,"threshold_uncertainty_score":0.016710281},"labels":[],"label_agreement":null},{"id":"W2077822383","doi":"10.1073/pnas.0805291105","title":"A <i>Drosophila</i> model for Angelman syndrome","year":2008,"lang":"en","type":"article","venue":"Proceedings of the National Academy of Sciences","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","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":"University of Alberta","funders":"Eunice Kennedy Shriver National Institute of Child Health and Human Development; National Institute of Neurological Disorders and Stroke; National Institute of Mental Health; Howard Hughes Medical Institute","keywords":"UBE3A; Angelman syndrome; Mushroom bodies; Ubiquitin ligase; Biology; Ubiquitin; Genetics; Loss function; Ataxia; Neurodevelopmental disorder; Missense mutation; Null allele; Drosophila melanogaster; Drosophila (subgenus); Mutation; Mutant; Cell biology; Neuroscience; Gene; Phenotype","score_opus":0.049485525106867545,"score_gpt":0.28896140075838656,"score_spread":0.239475875651519,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2077822383","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.7437636,0.015698245,0.069544554,0.011210196,0.0030947337,0.003267409,0.064751,0.0055122315,0.08315809],"genre_scores_gemma":[0.7053987,0.011024304,0.10917961,0.004776964,0.00027535888,0.003441325,0.045369014,0.0010110127,0.11952369],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99968183,0.000055111243,0.000044040116,0.00007643306,0.000096691874,0.00004586738],"domain_scores_gemma":[0.9998535,0.000018699317,0.00004166645,0.000019510002,0.000017119492,0.00004940229],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00025599543,0.0014184423,0.0005526272,0.00080628565,0.0009344349,0.00047980508,0.0010011995,0.0012647778,0.0097608045],"category_scores_gemma":[0.00012387357,0.00028479178,0.00070450193,0.0004592131,0.00054882467,0.0005214153,0.0005220243,0.0018609725,0.0038538768],"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":[0.0005768928,0.00040138603,0.0010327571,0.00041596478,0.000064535685,0.0013214379,0.00013004949,0.0005005301,0.96143323,0.010163395,0.014410499,0.009549278],"study_design_scores_gemma":[0.00075451384,0.0021301971,0.014770695,0.00027819423,0.00026113575,0.0076314327,0.00028720772,0.008896686,0.42279798,0.0037832826,0.5382745,0.00013420045],"about_ca_topic_score_codex":0.0024932043,"about_ca_topic_score_gemma":0.0033004107,"teacher_disagreement_score":0.0097608045,"about_ca_system_score_codex":0.0009139551,"about_ca_system_score_gemma":0.00045169733,"threshold_uncertainty_score":0.032653093},"labels":[],"label_agreement":null},{"id":"W2079253705","doi":"10.1111/j.1399-0004.2010.01443.x","title":"The utility of quantitative methylation assays at imprinted genes for the diagnosis of fetal and placental disorders","year":2010,"lang":"en","type":"article","venue":"Clinical Genetics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":35,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Child and Family Research Institute; University of British Columbia","funders":"Canadian Institutes of Health Research","keywords":"Genomic imprinting; Methylation; Biology; Epigenetics; Differentially methylated regions; DNA methylation; Genetics; Gene; Chromosome; Placenta; Fetus; Gene expression; Pregnancy","score_opus":0.04354641001633599,"score_gpt":0.36514203586032823,"score_spread":0.32159562584399226,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2079253705","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.79360825,0.007246166,0.18740092,0.0002827861,0.00009708646,0.00018150665,0.0034800111,0.0010449928,0.0066583487],"genre_scores_gemma":[0.90288675,0.0014890549,0.093001634,0.00014301151,0.000028719944,0.00012121219,0.00084252475,0.000039477083,0.0014476636],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9986481,0.00051451573,0.000083883766,0.0002813212,0.00040583292,0.000066278335],"domain_scores_gemma":[0.9986719,0.0008063046,0.00018435175,0.00013596435,0.00013625344,0.00006527176],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0015060883,0.00048283918,0.00024353986,0.0017462814,0.00011454027,0.00035153126,0.00037482133,0.00035749833,0.00084430125],"category_scores_gemma":[0.0032002646,0.0002696043,0.00018504569,0.00052772334,0.00038207896,0.00018649107,0.0002792333,0.00049206015,0.00027036443],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00061278103,0.000059733797,0.053888682,0.00015337595,0.000087112974,0.00019144331,0.00010704497,0.0013552604,0.89053035,0.00047164017,0.00022244184,0.05232009],"study_design_scores_gemma":[0.000044595963,0.0008628988,0.22553952,0.000053526895,0.00013947533,0.0037273176,0.00012605175,0.022802435,0.74191535,0.0012471201,0.0034803143,0.00006143418],"about_ca_topic_score_codex":0.0007610567,"about_ca_topic_score_gemma":0.0010841412,"teacher_disagreement_score":0.0017462814,"about_ca_system_score_codex":0.0002286913,"about_ca_system_score_gemma":0.00016394454,"threshold_uncertainty_score":0.007965088},"labels":[],"label_agreement":null},{"id":"W2080324075","doi":"10.1016/j.placenta.2004.01.020","title":"Genes and Development—A Workshop Report","year":2004,"lang":"en","type":"article","venue":"Placenta","topic":"Genetic Syndromes and Imprinting","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":"University of Calgary","funders":"","keywords":"Placenta; Biology; Function (biology); Genetically modified mouse; Phenotype; Computational biology; Transgene; Gene; Cell biology; Genetics; Pregnancy; Fetus","score_opus":0.015639742112461275,"score_gpt":0.24856034879075967,"score_spread":0.2329206066782984,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2080324075","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":[0.0327876,0.23890135,0.019972261,0.15215498,0.4225133,0.0013679054,0.0028719394,0.0007812642,0.12864946],"genre_scores_gemma":[0.08745424,0.14612891,0.012850419,0.019194927,0.108770594,0.0009980812,0.005420636,0.00046311025,0.61871916],"study_design_codex":"not_applicable","study_design_gemma":"not_applicable","domain_scores_codex":[0.999062,0.00013580605,0.00004538027,0.00013195453,0.00034358492,0.00028122932],"domain_scores_gemma":[0.9984224,0.00011453103,0.000046773286,0.000042005468,0.00038461725,0.0009896245],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.003592486,0.0017035495,0.00066866376,0.0013727086,0.001032711,0.0029881685,0.0017188706,0.0033507068,0.016556539],"category_scores_gemma":[0.0010549086,0.0003830058,0.0008885713,0.0009765262,0.0005770653,0.0017398156,0.00461961,0.0031405615,0.007948384],"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":[0.0006159242,0.00044048353,0.0010254576,0.0007423105,0.00006474568,0.001851424,0.00048277364,0.0006715499,0.011779411,0.004911047,0.81858563,0.15882923],"study_design_scores_gemma":[0.00006341378,0.00024015267,0.0011104145,0.00024037079,0.00003384311,0.0005796064,0.00047535019,0.00017867459,0.004026488,0.0014294969,0.99159884,0.000023264465],"about_ca_topic_score_codex":0.0016673704,"about_ca_topic_score_gemma":0.003909242,"teacher_disagreement_score":0.016556539,"about_ca_system_score_codex":0.0011629482,"about_ca_system_score_gemma":0.0030084949,"threshold_uncertainty_score":0.05538714},"labels":[],"label_agreement":null},{"id":"W2080361063","doi":"10.1002/ajmg.a.36490","title":"A cryptic familial rearrangement of 11p15.5, involving both imprinting centers, in a family with a history of short stature","year":2014,"lang":"en","type":"article","venue":"American Journal of Medical Genetics Part A","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":10,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Child and Family Research Institute; University of British Columbia","funders":"","keywords":"Imprinting (psychology); Short stature; Genomic imprinting; Family history; Genetics; Psychology; Medicine; Biology; Pediatrics; Internal medicine; Gene","score_opus":0.009875967680988498,"score_gpt":0.23778336149258597,"score_spread":0.22790739381159747,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2080361063","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9972464,0.0002539231,0.0014045974,0.00012835485,0.000018783716,0.000018392288,0.00007436306,0.00005106226,0.0008041343],"genre_scores_gemma":[0.9982681,0.00009957529,0.0005519793,0.00004713798,0.000015082576,0.0000055680343,0.000052891355,0.000006417514,0.00095315225],"study_design_codex":"case_report","study_design_gemma":"case_report","domain_scores_codex":[0.99982136,0.000023205484,0.000014222492,0.000070294765,0.000037603797,0.00003348844],"domain_scores_gemma":[0.9997688,0.000072246155,0.00005547404,0.000017811035,0.00001180382,0.00007398481],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00015689242,0.0010913064,0.00030014096,0.00095264363,0.0009625614,0.00022011976,0.00035100433,0.00068663526,0.002707904],"category_scores_gemma":[0.0006155613,0.00032399507,0.00042945548,0.00038046605,0.0005523502,0.00017697853,0.00042521278,0.0005767478,0.0002821481],"study_design_candidate":"case_report","study_design_consensus":"case_report","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0003594381,0.00022495947,0.16400583,0.0000806821,0.00013922201,0.6416511,0.0024360132,0.00053869176,0.16599171,0.0009101744,0.00070693874,0.022955231],"study_design_scores_gemma":[0.000039440365,0.00056897325,0.20669602,0.000025123843,0.00015105275,0.7720954,0.0003382171,0.0012016646,0.016495738,0.00027159406,0.0020848121,0.00003200372],"about_ca_topic_score_codex":0.0023942194,"about_ca_topic_score_gemma":0.0041835965,"teacher_disagreement_score":0.002707904,"about_ca_system_score_codex":0.00031124457,"about_ca_system_score_gemma":0.00026350372,"threshold_uncertainty_score":0.009058833},"labels":[],"label_agreement":null},{"id":"W2080675094","doi":"10.1016/j.gene.2012.01.027","title":"Loss of the Prader–Willi obesity syndrome protein necdin promotes adipogenesis","year":2012,"lang":"en","type":"article","venue":"Gene","topic":"Genetic Syndromes and Imprinting","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":"University of Alberta","funders":"Canadian Institutes of Health Research; Alberta Innovates","keywords":"Adipogenesis; Biology; Obesity; Transcription factor; Endocrinology; Receptor; Internal medicine; Gene; Cell biology; Adipose tissue; Biochemistry","score_opus":0.010178052027303734,"score_gpt":0.21682648000981516,"score_spread":0.20664842798251143,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2080675094","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99547654,0.0006571059,0.0021516678,0.00009649205,0.000021042131,0.0000040508335,0.00014759264,0.00005143681,0.0013940986],"genre_scores_gemma":[0.99645126,0.00038703388,0.0009719431,0.000022522103,0.0000045673332,0.0000068700783,0.00015894325,0.000027599237,0.0019693254],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99987364,0.000031285195,0.0000124223725,0.000025620215,0.000034153592,0.000022788461],"domain_scores_gemma":[0.9997501,0.00007151209,0.000069837864,0.00004013918,0.000010306431,0.000058184738],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.000114859205,0.0002864791,0.00017494772,0.00032410226,0.00012844396,0.00030059545,0.00020417024,0.00021809916,0.0016452327],"category_scores_gemma":[0.00025224686,0.00022088145,0.00014945684,0.00014859046,0.00043866696,0.00019857385,0.000535536,0.00055193045,0.0003091785],"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":[0.00018849463,0.000007873951,0.0009241365,0.000011188836,0.0000067700175,0.00042058653,0.000010177064,0.00009759454,0.9971058,0.00028436576,0.00002897379,0.00091406016],"study_design_scores_gemma":[0.000034004926,0.000111568705,0.026304033,0.000007890281,0.00003324211,0.0029246197,0.0000647722,0.0014736615,0.96632063,0.00023893132,0.002478451,0.00000827902],"about_ca_topic_score_codex":0.00047514925,"about_ca_topic_score_gemma":0.0009497739,"teacher_disagreement_score":0.0016452327,"about_ca_system_score_codex":0.00024111691,"about_ca_system_score_gemma":0.00016867848,"threshold_uncertainty_score":0.005503893},"labels":[],"label_agreement":null},{"id":"W2080676561","doi":"10.1007/s00439-012-1207-x","title":"Mutations in the sarcosine dehydrogenase gene in patients with sarcosinemia","year":2012,"lang":"en","type":"article","venue":"Human Genetics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","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":"Université de Sherbrooke","funders":"","keywords":"Biology; Sarcosine; Human genetics; Genetics; Gene; Molecular medicine; Metabolic disease; Computational biology; Endocrinology; Amino acid; Glycine","score_opus":0.01178772805927869,"score_gpt":0.2426123216915446,"score_spread":0.2308245936322659,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2080676561","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99835545,0.00018989282,0.0003077879,0.00013198389,0.000013242889,0.0000050638328,0.000067289504,0.000016572296,0.0009126946],"genre_scores_gemma":[0.99957746,0.00006719784,0.00014479631,0.000018938501,0.000013267295,0.0000020394853,0.000032886448,0.0000038089597,0.00013962825],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9997545,0.00003885571,0.000041136715,0.00006298435,0.000060936425,0.000041665822],"domain_scores_gemma":[0.99950457,0.00020937796,0.00012494532,0.000022170605,0.00004100307,0.00009794088],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00021400281,0.0011671403,0.00039343323,0.0014486485,0.0007261899,0.00036490112,0.00038468005,0.0012849383,0.0017687945],"category_scores_gemma":[0.0015388457,0.0003035155,0.0002795916,0.00083510735,0.0006342754,0.00034178948,0.00038040403,0.0003835036,0.00021220885],"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":[0.0016855131,0.00016995122,0.5102677,0.000096515905,0.00015138769,0.37727556,0.0019677859,0.00124218,0.09365116,0.0012027286,0.0007753973,0.011514157],"study_design_scores_gemma":[0.00010852721,0.0005070723,0.43462554,0.000037893322,0.00028091087,0.542961,0.00096315576,0.0023179117,0.015611445,0.0011470385,0.0013728739,0.0000665417],"about_ca_topic_score_codex":0.0013091224,"about_ca_topic_score_gemma":0.0010175514,"teacher_disagreement_score":0.0017687945,"about_ca_system_score_codex":0.00026032017,"about_ca_system_score_gemma":0.00029735712,"threshold_uncertainty_score":0.0059171915},"labels":[],"label_agreement":null},{"id":"W2080876236","doi":"10.1016/j.jpeds.2003.09.049","title":"Sudden death in growth hormone–treated children with Prader-Willi syndrome","year":2004,"lang":"en","type":"review","venue":"The Journal of Pediatrics","topic":"Genetic Syndromes and Imprinting","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":"Centre Hospitalier Universitaire Sainte-Justine; Université de Montréal","funders":"","keywords":"Medicine; Autopsy; Growth hormone; Bronchopneumonia; Pediatrics; Apnea; Growth hormone treatment; Hormone; Growth retardation; Sudden death; Cause of death; Internal medicine; Disease; Pregnancy","score_opus":0.015103356636278119,"score_gpt":0.25640263626346743,"score_spread":0.2412992796271893,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2080876236","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":[0.003883788,0.9909418,0.0009412872,0.00086561264,0.0008129786,0.000009349994,0.000040682593,0.00003351978,0.002471039],"genre_scores_gemma":[0.02005438,0.97592473,0.0005981054,0.0006323433,0.0016026667,0.000017102799,0.00011161235,0.0000072229923,0.0010518832],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.9998566,0.00003283251,0.000027101769,0.000025140882,0.000042866362,0.000015412079],"domain_scores_gemma":[0.9996842,0.0001749521,0.00005767586,0.00000763889,0.000038577287,0.000036899346],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00029784316,0.0006621917,0.0013183508,0.0010227389,0.00019416725,0.0004950442,0.000844105,0.0010634313,0.00094691105],"category_scores_gemma":[0.0009134667,0.00015766942,0.00037209917,0.0006910925,0.0003715781,0.0003217775,0.0003667075,0.0009869325,0.0006923038],"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":[0.00029651847,0.00008715981,0.008036878,0.00526354,0.00027804295,0.03953934,0.00013621474,0.0005510813,0.002186343,0.0017319431,0.033627186,0.90826565],"study_design_scores_gemma":[0.00040260985,0.0005128614,0.035235446,0.0048254197,0.0012841666,0.37556708,0.0004340894,0.00062942505,0.0031457916,0.0027901283,0.5750661,0.00010690223],"about_ca_topic_score_codex":0.0007259179,"about_ca_topic_score_gemma":0.0011877397,"teacher_disagreement_score":0.0013183508,"about_ca_system_score_codex":0.00031004957,"about_ca_system_score_gemma":0.00048034507,"threshold_uncertainty_score":0.0031677485},"labels":[],"label_agreement":null},{"id":"W2082827707","doi":"10.1071/rd06118","title":"Gene expression and maintenance of pregnancy in bovine: roles of trophoblastic binucleate cell-specific molecules","year":2006,"lang":"en","type":"article","venue":"Reproduction Fertility and Development","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":57,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Health Sciences Centre; University of Calgary","funders":"","keywords":"Biology; Placentation; Placental lactogen; Pregnancy; Gene expression; Placenta; Cell biology; Microarray analysis techniques; Cell; Gene; Fetus; Genetics","score_opus":0.008195366511169309,"score_gpt":0.1976218719923018,"score_spread":0.1894265054811325,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2082827707","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.98814756,0.0069672437,0.0030004603,0.000081204686,0.00001173966,0.000012884645,0.0005258876,0.00003012889,0.0012228232],"genre_scores_gemma":[0.9917036,0.0025781146,0.0028280464,0.00005327066,0.000011428482,0.000025486252,0.0006396864,0.000014118645,0.002146125],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9999033,0.000016899712,0.0000054130132,0.000033131982,0.00001907759,0.000022152877],"domain_scores_gemma":[0.9998847,0.000030423209,0.00003249922,0.000009594887,0.00001538473,0.000027325887],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00013569936,0.00015720555,0.00018884966,0.0003791226,0.00019307596,0.0004049958,0.00009017628,0.00019791434,0.0007346561],"category_scores_gemma":[0.00016187408,0.00009771326,0.00009341305,0.00029237042,0.0002534793,0.00024171997,0.000137922,0.00021713949,0.0001946195],"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":[0.00010229143,0.000004250299,0.0018606231,0.000037405393,0.0000033445042,0.000044336924,0.00007400232,0.000036483187,0.9952567,0.00010484541,0.000014429606,0.0024613172],"study_design_scores_gemma":[0.000020484425,0.00057689013,0.5691395,0.000046823807,0.00007579986,0.0010872963,0.0006942205,0.0013373336,0.41466948,0.00043820357,0.011888926,0.000025170142],"about_ca_topic_score_codex":0.0017132359,"about_ca_topic_score_gemma":0.002552046,"teacher_disagreement_score":0.0017132359,"about_ca_system_score_codex":0.00034223095,"about_ca_system_score_gemma":0.000205466,"threshold_uncertainty_score":0.003406465},"labels":[],"label_agreement":null},{"id":"W2084601112","doi":"10.1016/j.placenta.2005.07.004","title":"Unbalanced Placental Expression of Imprinted Genes in Human Intrauterine Growth Restriction","year":2005,"lang":"en","type":"article","venue":"Placenta","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":300,"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":"Genomic imprinting; Biology; MEG3; Intrauterine growth restriction; Endocrinology; Internal medicine; Placenta; Gene expression; DNA methylation; Microarray analysis techniques; Andrology; Gene; Fetus; Genetics; RNA; Medicine; Pregnancy; Long non-coding RNA","score_opus":0.0076232740461057045,"score_gpt":0.24546667790580262,"score_spread":0.2378434038596969,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2084601112","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9801926,0.012194563,0.0030958555,0.0003238569,0.000045625973,0.000007887909,0.00019342842,0.00008410368,0.0038621507],"genre_scores_gemma":[0.99665916,0.0022631206,0.00048842,0.000023413111,0.000020479534,0.000004861385,0.000067300534,0.000009694128,0.0004636327],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.99987495,0.000040167666,0.000015229404,0.000018629975,0.000031996464,0.000019069736],"domain_scores_gemma":[0.99973065,0.000117728414,0.000067160785,0.0000307674,0.000017744473,0.000035919624],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00023466976,0.000263221,0.00024570775,0.0013536672,0.00021774364,0.00047426662,0.0002765832,0.0002897031,0.0008676002],"category_scores_gemma":[0.0007977559,0.00030687233,0.00009540026,0.0006888112,0.000722825,0.0002908183,0.00036574813,0.0003323019,0.00013927437],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0033556412,0.000050956507,0.037618726,0.00033433764,0.00010178136,0.021107139,0.00068725226,0.0014982723,0.892832,0.011081174,0.00046559927,0.030867111],"study_design_scores_gemma":[0.00017001678,0.00047961867,0.27534312,0.00006966816,0.00044279348,0.055278547,0.0008889445,0.0034401242,0.63608485,0.015092871,0.01266121,0.00004818594],"about_ca_topic_score_codex":0.00065250456,"about_ca_topic_score_gemma":0.0003628392,"teacher_disagreement_score":0.0013536672,"about_ca_system_score_codex":0.00031014948,"about_ca_system_score_gemma":0.00018272587,"threshold_uncertainty_score":0.0029024482},"labels":[],"label_agreement":null},{"id":"W2084698702","doi":"10.1053/beog.2000.0107","title":"Confined placental mosaicism and genomic imprinting","year":2000,"lang":"en","type":"review","venue":"Best Practice & Research Clinical Obstetrics & Gynaecology","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","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":"B.C. Women's Hospital & Health Centre; University of British Columbia","funders":"","keywords":"Uniparental disomy; Genomic imprinting; Angelman syndrome; Imprinting (psychology); Genetics; Mendelian inheritance; Non-Mendelian inheritance; Beckwith–Wiedemann syndrome; Germline mosaicism; Placenta; Biology; Medicine; Chromosome; Karyotype; Fetus; Mutation; Pregnancy; Gene; DNA methylation","score_opus":0.138468466168502,"score_gpt":0.4726787761983441,"score_spread":0.3342103100298421,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2084698702","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":[0.00017532294,0.99742955,0.00026045082,0.0005638618,0.0002510205,0.000002520087,0.000009489119,0.000007645335,0.001300038],"genre_scores_gemma":[0.0015750652,0.99627507,0.0003460164,0.00033635052,0.00050921633,0.0000055552114,0.00002416805,0.0000016142692,0.00092687],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.9997812,0.000050201717,0.000029172246,0.000041484585,0.0000797123,0.0000181433],"domain_scores_gemma":[0.99953425,0.00028770347,0.000053730066,0.000017394957,0.00007099055,0.000035890072],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00075434207,0.0009106589,0.0015258837,0.0021726575,0.00022771108,0.0010613621,0.0010092004,0.0015027233,0.0023344718],"category_scores_gemma":[0.0014151892,0.00030186336,0.00021364378,0.002372492,0.0012319125,0.001124385,0.0005820814,0.0014801028,0.0009802493],"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":[0.00009163744,0.000039456547,0.0007182968,0.005022053,0.00006461441,0.00218992,0.00006892831,0.00054710195,0.001400713,0.0057438733,0.039549258,0.94456404],"study_design_scores_gemma":[0.00004995778,0.00004355127,0.0019878116,0.0024624262,0.0001404212,0.017145809,0.00016983434,0.00015977102,0.0006991094,0.005654344,0.97146153,0.000025324785],"about_ca_topic_score_codex":0.0018512752,"about_ca_topic_score_gemma":0.0032372875,"teacher_disagreement_score":0.0023344718,"about_ca_system_score_codex":0.000845154,"about_ca_system_score_gemma":0.0011712059,"threshold_uncertainty_score":0.0078095794},"labels":[],"label_agreement":null},{"id":"W2085263711","doi":"10.1159/000118545","title":"Abnormal Food-Seeking Behavior after Surgery for Craniopharyngioma","year":2008,"lang":"en","type":"article","venue":"Neuropsychobiology","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":45,"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; Douglas Mental Health University Institute; Montreal General Hospital","funders":"","keywords":"Craniopharyngioma; Feeding behavior; Obesity; Eating behavior; Food intake; Psychology; Foraging; Medicine; Surgery; Endocrinology; Biology","score_opus":0.0212507388158746,"score_gpt":0.24675655815751413,"score_spread":0.22550581934163952,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2085263711","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9982206,0.00041834245,0.000308077,0.00010294222,0.00002551376,0.00002362204,0.00004751032,0.00003579317,0.0008176528],"genre_scores_gemma":[0.99923813,0.00015002055,0.00016291643,0.000075220705,0.000019819572,0.0000094627,0.00005677848,0.0000063015223,0.0002815328],"study_design_codex":"case_report","study_design_gemma":"case_report","domain_scores_codex":[0.9997768,0.000016529391,0.00002047434,0.00003382873,0.000039139864,0.000113253125],"domain_scores_gemma":[0.9991441,0.00014105446,0.00030498844,0.0000636868,0.00003702513,0.0003090907],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00011329712,0.0011583583,0.0007215339,0.0010900269,0.0014611002,0.00042360462,0.00042543924,0.0013385651,0.00069797493],"category_scores_gemma":[0.001208628,0.00052524806,0.00061706855,0.0006168143,0.0015661698,0.00024433996,0.0006528296,0.0012915283,0.00022995837],"study_design_candidate":"case_report","study_design_consensus":"case_report","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00036850377,0.00026781874,0.20327781,0.00004833049,0.00008063663,0.77884066,0.0011722344,0.00026873956,0.0087176105,0.00016817759,0.00035856417,0.0064307805],"study_design_scores_gemma":[0.000042441585,0.00082345924,0.26195028,0.000012387149,0.000046555215,0.7341157,0.00039798516,0.00024034824,0.0015360628,0.00020852505,0.00056689524,0.00005930575],"about_ca_topic_score_codex":0.0048120515,"about_ca_topic_score_gemma":0.0067413775,"teacher_disagreement_score":0.0048120515,"about_ca_system_score_codex":0.0008021803,"about_ca_system_score_gemma":0.0004594329,"threshold_uncertainty_score":0.009568095},"labels":[],"label_agreement":null},{"id":"W2086084923","doi":"10.1007/s004280100509","title":"Promoter-specific transcription of the IGF2 gene: a novel rapid, non-radioactive and highly sensitive protocol for mRNA analysis","year":2001,"lang":"en","type":"article","venue":"Archiv für Pathologische Anatomie und Physiologie und für Klinische Medicin","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","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":"McGill University; Jewish General Hospital","funders":"Deutsche Forschungsgemeinschaft","keywords":"Biology; Molecular biology; Genomic imprinting; Gene expression; Gene; Promoter; Messenger RNA; Northern blot; RNA; Insulin-like growth factor 2; Ribonuclease; Transcription (linguistics); Genetics","score_opus":0.030873603737841742,"score_gpt":0.33033961654090543,"score_spread":0.2994660128030637,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2086084923","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":[0.041181803,0.002281137,0.946889,0.00033948172,0.00044744904,0.0010775755,0.0019770726,0.0026118334,0.003194694],"genre_scores_gemma":[0.1171361,0.002207605,0.8487655,0.00046554365,0.00020993885,0.003248827,0.009191689,0.0014361966,0.01733872],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99873203,0.00029484034,0.00008291235,0.000304588,0.00036731779,0.00021839724],"domain_scores_gemma":[0.99923885,0.00032034636,0.00005899372,0.00013812039,0.00012304261,0.00012064205],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0013525906,0.0017736516,0.0013238222,0.0015485635,0.0007383529,0.0006791377,0.0013293909,0.0008440993,0.0027318033],"category_scores_gemma":[0.0010606005,0.001108264,0.0010893579,0.00075379125,0.0014131765,0.0005627665,0.0012428606,0.0034361458,0.0027574769],"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":[0.00012967741,0.000026834943,0.00006862686,0.00011765572,0.000008645263,0.000043409906,0.000041396983,0.00010332368,0.99362683,0.0004803808,0.000512139,0.004841026],"study_design_scores_gemma":[0.00006703495,0.00018355394,0.00082942616,0.000037374026,0.000039585182,0.00031697075,0.000021085958,0.0019307041,0.9802429,0.00046932217,0.015820898,0.0000410789],"about_ca_topic_score_codex":0.002052362,"about_ca_topic_score_gemma":0.0072991904,"teacher_disagreement_score":0.0027318033,"about_ca_system_score_codex":0.0010627644,"about_ca_system_score_gemma":0.0020040628,"threshold_uncertainty_score":0.009138763},"labels":[],"label_agreement":null},{"id":"W2086493068","doi":"10.1016/j.cjca.2012.05.018","title":"Coronary Artery Dissection in Prader–Willi Syndrome: Case Report and Literature Review","year":2012,"lang":"en","type":"review","venue":"Canadian Journal of Cardiology","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":5,"is_retracted":false,"has_abstract":false,"route_ca_aff":false,"route_ca_fund":false,"route_ca_venue":true,"route_about_ca":false,"ca_institutions":"","funders":"","keywords":"Medicine; Artery dissection; Dissection (medical); Cardiology; Myocardial infarction; Internal medicine; Artery; Hypoxemia; Right coronary artery; Acute coronary syndrome; Surgery; Coronary angiography","score_opus":0.020140795290613057,"score_gpt":0.273911714645204,"score_spread":0.2537709193545909,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2086493068","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":[0.004211672,0.99077773,0.00068681565,0.0011573547,0.0004637125,0.0000145406775,0.00007974669,0.00003166576,0.0025768217],"genre_scores_gemma":[0.015002505,0.98060375,0.0010907563,0.00061943196,0.0015769493,0.000010620051,0.00015515201,0.00000651155,0.00093433633],"study_design_codex":"design_other","study_design_gemma":"case_report","domain_scores_codex":[0.9997559,0.00003117064,0.00006988971,0.000055236556,0.000054768614,0.000033067474],"domain_scores_gemma":[0.999468,0.0002600088,0.00011075007,0.000017716919,0.00006774118,0.00007561017],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0003310974,0.0010985547,0.0016417556,0.0038038709,0.00042838725,0.0012827513,0.0013868494,0.0016092958,0.0021461658],"category_scores_gemma":[0.00093712576,0.00039472553,0.0006457006,0.0025963665,0.0007758877,0.0021015182,0.0007909381,0.0012501272,0.0009647419],"study_design_candidate":"case_report","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0001586921,0.00017936646,0.008273381,0.014587826,0.00035563705,0.2662558,0.00047473065,0.0008304062,0.004433733,0.0020266904,0.050578382,0.65184534],"study_design_scores_gemma":[0.000044727643,0.0000869277,0.0078020943,0.00415702,0.0006572999,0.73793805,0.0007127697,0.0003065162,0.0007646074,0.001952866,0.24547307,0.000103959384],"about_ca_topic_score_codex":0.0011048565,"about_ca_topic_score_gemma":0.002121319,"teacher_disagreement_score":0.0038038709,"about_ca_system_score_codex":0.0004632752,"about_ca_system_score_gemma":0.0009821141,"threshold_uncertainty_score":0.007179618},"labels":[],"label_agreement":null},{"id":"W2086864499","doi":"10.1017/s0140525x08004317","title":"Imprinting and psychiatric genetics: Beware the diagnostic phenotype","year":2008,"lang":"en","type":"article","venue":"Behavioral and Brain Sciences","topic":"Genetic Syndromes and Imprinting","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; Hospital for Sick Children","funders":"","keywords":"GRASP; Imprinting (psychology); Phenotype; Psychology; Predictive power; Genomic imprinting; Genetics; Biology; Neuroscience; Gene; Computer science; Epistemology; Philosophy","score_opus":0.028770502137624013,"score_gpt":0.286319976345389,"score_spread":0.25754947420776503,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2086864499","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":[0.046019547,0.04484023,0.01119679,0.86590534,0.010535227,0.00003281569,0.00012389947,0.00033852822,0.02100758],"genre_scores_gemma":[0.86908424,0.024626331,0.008374356,0.06788797,0.02097437,0.000029231656,0.000067329536,0.00007206032,0.008884013],"study_design_codex":"design_other","study_design_gemma":"theoretical_or_conceptual","domain_scores_codex":[0.99921656,0.00042972952,0.000055319175,0.00004770808,0.00020923262,0.0000414214],"domain_scores_gemma":[0.99666095,0.0020868008,0.00031511838,0.00029170158,0.0002815827,0.000363928],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0022406634,0.00027744073,0.00036270433,0.000804302,0.0003891237,0.0011345559,0.0006111469,0.002585766,0.0025251037],"category_scores_gemma":[0.015218363,0.00012470948,0.00010474665,0.00023094715,0.0052350904,0.0028900797,0.0009399345,0.0025220045,0.00062717666],"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":[0.00045477258,0.0002468601,0.10224105,0.0006083693,0.00012019978,0.013208058,0.002496483,0.00071469764,0.0051456955,0.23242359,0.2158772,0.42646304],"study_design_scores_gemma":[0.00012030475,0.00023532771,0.036771122,0.0010207791,0.000094455834,0.036694203,0.003296803,0.0023119836,0.0017316707,0.7984868,0.11914344,0.000093069866],"about_ca_topic_score_codex":0.0006301771,"about_ca_topic_score_gemma":0.0010743933,"teacher_disagreement_score":0.002585766,"about_ca_system_score_codex":0.00048526193,"about_ca_system_score_gemma":0.0007864644,"threshold_uncertainty_score":0.01184988},"labels":[],"label_agreement":null},{"id":"W2089207825","doi":"10.1038/mp.2011.157","title":"Genome-wide association study meta-analysis of European and Asian-ancestry samples identifies three novel loci associated with bipolar disorder","year":2011,"lang":"en","type":"article","venue":"Molecular Psychiatry","topic":"Genetic Syndromes and Imprinting","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":"University of Toronto","funders":"","keywords":"Genome-wide association study; Single-nucleotide polymorphism; Genetic association; Genetics; Biology; SNP; Locus (genetics); Meta-analysis; Multiple comparisons problem; Candidate gene; Gene; Medicine; Genotype; Internal medicine","score_opus":0.03286568714207273,"score_gpt":0.24576275200771822,"score_spread":0.21289706486564547,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2089207825","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.98833036,0.006873098,0.0026596033,0.00038234072,0.00009751394,0.000015497137,0.0006327047,0.00007595031,0.0009329089],"genre_scores_gemma":[0.9981766,0.0006984835,0.00062906934,0.00006511091,0.000029371473,0.000007444289,0.00020441695,0.000017923234,0.0001715529],"study_design_codex":"observational","study_design_gemma":"meta_analysis","domain_scores_codex":[0.997849,0.0008425073,0.00020303475,0.0007217695,0.00019183222,0.00019186773],"domain_scores_gemma":[0.9975994,0.001159144,0.0004650095,0.00037245062,0.00016156785,0.00024242274],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0026877553,0.0015556122,0.0015003628,0.0018384203,0.0009461697,0.0016096254,0.001110065,0.0012572543,0.0022303944],"category_scores_gemma":[0.0035115285,0.00077397726,0.004133542,0.0027700658,0.0007110053,0.00052714016,0.0009877454,0.0012095568,0.00016187083],"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":[0.0042425944,0.00008381835,0.94069993,0.00020369247,0.035995245,0.001251609,0.00034005535,0.00063392165,0.009170565,0.00033416128,0.00054015,0.006504312],"study_design_scores_gemma":[0.0003330742,0.00023584823,0.9668889,0.00006129804,0.026847702,0.0011248847,0.00030702294,0.0018659179,0.001080564,0.00066002674,0.00056003616,0.00003467973],"about_ca_topic_score_codex":0.008449301,"about_ca_topic_score_gemma":0.010597628,"teacher_disagreement_score":0.008449301,"about_ca_system_score_codex":0.00034536215,"about_ca_system_score_gemma":0.0004957091,"threshold_uncertainty_score":0.016800284},"labels":[],"label_agreement":null},{"id":"W2089831021","doi":"10.1016/j.ygeno.2005.05.015","title":"Detailed analysis of the methylation patterns of the KvDMR1 imprinting control region of human chromosome 11","year":2005,"lang":"en","type":"article","venue":"Genomics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","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":"University of Toronto","funders":"Canadian Institutes of Health Research","keywords":"Biology; Imprinting (psychology); Genetics; Genomic imprinting; Methylation; DNA methylation; Chromosome; Computational biology; Gene; Gene expression","score_opus":0.009979110336141121,"score_gpt":0.23016050058611595,"score_spread":0.22018139024997482,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2089831021","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9850578,0.0032303832,0.0069699823,0.00014466669,0.000012523244,0.000021813757,0.0020631356,0.00008460122,0.0024149972],"genre_scores_gemma":[0.99183226,0.00093266816,0.0034551334,0.0000295591,0.0000041348135,0.000013084662,0.0017345466,0.000024709121,0.0019737678],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9999453,0.0000063974235,0.0000031874736,0.000020099473,0.000010398036,0.000014648682],"domain_scores_gemma":[0.99993145,0.0000204273,0.000016555094,0.000009705812,0.000009407053,0.000012380063],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.000072749855,0.00018382419,0.00019353104,0.00036183937,0.00016577034,0.00017947987,0.00014976512,0.00012070222,0.0014514233],"category_scores_gemma":[0.0001643518,0.0001687866,0.0001718938,0.000252205,0.00011226835,0.000107933614,0.00013666705,0.0002590409,0.0002727817],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00017414441,0.000006134432,0.0022699547,0.00004831966,0.000022435097,0.000081862905,0.000040985567,0.00021739503,0.9924959,0.00017150586,0.000048715636,0.0044226334],"study_design_scores_gemma":[0.000023415056,0.0001489643,0.18710153,0.000011807889,0.00013021452,0.0013770877,0.00009312209,0.0016078795,0.801642,0.00045652897,0.0073879524,0.000019513569],"about_ca_topic_score_codex":0.0029943415,"about_ca_topic_score_gemma":0.0057230545,"teacher_disagreement_score":0.0029943415,"about_ca_system_score_codex":0.00021859839,"about_ca_system_score_gemma":0.0001728024,"threshold_uncertainty_score":0.0059537888},"labels":[],"label_agreement":null},{"id":"W2090074407","doi":"10.1038/sj.ejhg.5201353","title":"Patients with familial biparental hydatidiform moles have normal methylation at imprinted genes","year":2005,"lang":"en","type":"article","venue":"European Journal of Human Genetics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":23,"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; Centre Hospitalier de l’Université de Montréal","funders":"Canadian Institutes of Health Research","keywords":"Genomic imprinting; Methylation; Biology; Molar pregnancy; DNA methylation; Genetics; Reprogramming; Allele; Differentially methylated regions; Gene; Imprinting (psychology); Pregnancy; Gene expression; Gestation","score_opus":0.010379121268311238,"score_gpt":0.22698347084036158,"score_spread":0.21660434957205035,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2090074407","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99650455,0.00045106796,0.00064957753,0.00014990936,0.000025701973,0.000008463212,0.00021611479,0.000059668044,0.0019350202],"genre_scores_gemma":[0.9991528,0.0001164746,0.00022653602,0.000028939918,0.000021223175,0.000004689206,0.00009787831,0.00001062422,0.00034083286],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9997166,0.000050301263,0.00004127674,0.00005767547,0.00006139065,0.00007283489],"domain_scores_gemma":[0.9991015,0.00038896847,0.00022838096,0.000088721674,0.000053771688,0.00013865552],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00021457755,0.001139928,0.00077973044,0.0010024245,0.0007149156,0.00040952157,0.0002900361,0.00080441777,0.0036476224],"category_scores_gemma":[0.002705461,0.00042317738,0.00023918692,0.00088477577,0.0007360528,0.00042421804,0.000517467,0.00034441374,0.00042811988],"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":[0.0034124008,0.00014532912,0.5445739,0.000269712,0.00029348332,0.28031626,0.0037858621,0.00075428095,0.13092558,0.0014082054,0.0015835327,0.03253149],"study_design_scores_gemma":[0.00011234155,0.00041677261,0.4040628,0.000017528282,0.00022259979,0.57306224,0.0007966259,0.0006822667,0.01684778,0.0009808067,0.002751514,0.000046737052],"about_ca_topic_score_codex":0.0006473394,"about_ca_topic_score_gemma":0.00064969267,"teacher_disagreement_score":0.0036476224,"about_ca_system_score_codex":0.00016001031,"about_ca_system_score_gemma":0.00015971002,"threshold_uncertainty_score":0.012202501},"labels":[],"label_agreement":null},{"id":"W2090165161","doi":"10.1007/s10815-012-9911-y","title":"G9a co-localized with histone H3 lysine 9 monomethylation but not dimethylation in a nuclear membrane-dependent manner during mouse preimplantation embryo development","year":2012,"lang":"en","type":"article","venue":"Journal of Assisted Reproduction and Genetics","topic":"Genetic Syndromes and Imprinting","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":"Institute of Genetics; Institute of Genetics and Developmental Biology, Chinese Academy of Sciences; Chinese Academy of Sciences","keywords":"Histone H3; Embryo; Lysine; Histone; Cell biology; Embryogenesis; Biology; Chemistry; Genetics; Amino acid; DNA","score_opus":0.015460726796294193,"score_gpt":0.2612567741001873,"score_spread":0.24579604730389307,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2090165161","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9806255,0.004271627,0.008993706,0.00045934453,0.00020238866,0.000031499447,0.00088978134,0.00023233003,0.004293866],"genre_scores_gemma":[0.98204076,0.0010067198,0.0038527786,0.00016522943,0.000024828714,0.00004614079,0.00097537634,0.00014817443,0.011739988],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9996686,0.00003440984,0.000021695869,0.000113723334,0.00007089366,0.00009063866],"domain_scores_gemma":[0.99976856,0.00003185441,0.000059936207,0.000031366897,0.000028995366,0.00007932113],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00014011783,0.0003482651,0.00032358328,0.00047894698,0.0004765027,0.00045993418,0.00045425596,0.00041039367,0.0019649456],"category_scores_gemma":[0.0001576266,0.00047905833,0.0004924994,0.000291068,0.00041009902,0.00039365512,0.00059093203,0.0010047944,0.0013098321],"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":[0.000089032685,0.0000040242294,0.00012829501,0.000011113225,0.0000045060983,0.00006418762,0.000010294907,0.000009167664,0.99929523,0.00007015119,0.000023483164,0.0002904352],"study_design_scores_gemma":[0.000010258316,0.000042168736,0.012893406,0.0000054135585,0.00002107658,0.00031256428,0.000053000615,0.00033338866,0.9840555,0.00006023974,0.0022059649,0.0000069437524],"about_ca_topic_score_codex":0.0019687458,"about_ca_topic_score_gemma":0.0038771087,"teacher_disagreement_score":0.0019687458,"about_ca_system_score_codex":0.0007379126,"about_ca_system_score_gemma":0.00034499838,"threshold_uncertainty_score":0.0065734386},"labels":[],"label_agreement":null},{"id":"W2090557879","doi":"10.1016/j.ydbio.2007.03.371","title":"The effect of superovulation on methylation and expression of imprinted genes in pre- and post-implantation mouse embryos","year":2007,"lang":"en","type":"article","venue":"Developmental Biology","topic":"Genetic Syndromes and Imprinting","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; Montreal Children's Hospital","funders":"","keywords":"Biology; Genomic imprinting; Embryo; Methylation; Andrology; Gene; DNA methylation; Imprinting (psychology); Genetics; Cell biology; Gene expression","score_opus":0.005118175458745296,"score_gpt":0.2511278387584135,"score_spread":0.2460096632996682,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2090557879","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9944956,0.0022027388,0.0009473658,0.00016515098,0.000044787343,0.000024873292,0.00043914522,0.000045087203,0.0016352638],"genre_scores_gemma":[0.9903098,0.0014701121,0.0010107377,0.00018883067,0.000048527927,0.000062323335,0.0006243628,0.00010015359,0.0061852224],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99968016,0.00008655214,0.000028574002,0.000047737907,0.00005462155,0.00010235945],"domain_scores_gemma":[0.99861395,0.0006807753,0.00020972136,0.00014642935,0.000055126868,0.0002939927],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0003855248,0.00046525963,0.0005240174,0.0006724217,0.0002271826,0.00037840425,0.0005958788,0.00039760215,0.0033518567],"category_scores_gemma":[0.00068734266,0.0004159741,0.00035820776,0.00025550436,0.0006079137,0.00040050034,0.00069558405,0.0012598605,0.00035399836],"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":[0.001547128,0.00003659948,0.00076567277,0.000029505678,0.000009292531,0.00009276731,0.000058539423,0.00006054969,0.9955349,0.0002310746,0.00003438029,0.0015996053],"study_design_scores_gemma":[0.000056020115,0.0009773162,0.017052136,0.000012398057,0.000028139311,0.00017097063,0.00010426693,0.0004213643,0.97984034,0.00018224043,0.0011404734,0.000014305804],"about_ca_topic_score_codex":0.0016858734,"about_ca_topic_score_gemma":0.0033757284,"teacher_disagreement_score":0.0033518567,"about_ca_system_score_codex":0.000385777,"about_ca_system_score_gemma":0.00040451888,"threshold_uncertainty_score":0.011213124},"labels":[],"label_agreement":null},{"id":"W2091833694","doi":"10.1016/j.placenta.2009.12.003","title":"Decreased Placental Methylation at the H19/IGF2 Imprinting Control Region is Associated with Normotensive Intrauterine Growth Restriction but not Preeclampsia","year":2010,"lang":"en","type":"article","venue":"Placenta","topic":"Genetic Syndromes and Imprinting","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; Child and Family Research Institute","funders":"Canadian Institutes of Health Research","keywords":"Genomic imprinting; Methylation; Placentation; DNA methylation; Intrauterine growth restriction; Biology; Preeclampsia; Imprinting (psychology); Differentially methylated regions; Epigenetics; Placenta; Andrology; Endocrinology; Candidate gene; Internal medicine; Fetus; Gene; Genetics; Gene expression; Pregnancy; Medicine","score_opus":0.0077119692239034894,"score_gpt":0.21060861554710228,"score_spread":0.2028966463231988,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2091833694","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.997382,0.00037054525,0.00076744426,0.00009952885,0.000012862945,0.000004533281,0.00027928333,0.000033712284,0.001050083],"genre_scores_gemma":[0.9990404,0.00013622276,0.00030896993,0.0000151372315,0.000017356544,0.0000045953348,0.00010847096,0.000010333629,0.00035843806],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9996239,0.000098137985,0.00003533338,0.00009430928,0.00009749488,0.000050817755],"domain_scores_gemma":[0.9983011,0.000563662,0.0007009914,0.00013589599,0.00007139387,0.00022703559],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.000248174,0.00043854403,0.00046197826,0.0023373975,0.00037253875,0.00030655798,0.0005634049,0.00038714384,0.0027810757],"category_scores_gemma":[0.0016618947,0.00027490722,0.00020535865,0.0011638341,0.0006713891,0.00015457813,0.0003114773,0.00044825254,0.00015946502],"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":[0.004561819,0.0001844169,0.61156994,0.00017710304,0.00036766523,0.023157805,0.00084721623,0.000521889,0.33812222,0.0011323115,0.0005233446,0.018834237],"study_design_scores_gemma":[0.000045827037,0.00023350368,0.9487583,0.000014150205,0.00017921899,0.025834845,0.00018143865,0.00068858004,0.02270296,0.0006773638,0.0006667849,0.000017019414],"about_ca_topic_score_codex":0.002544921,"about_ca_topic_score_gemma":0.0015788557,"teacher_disagreement_score":0.0027810757,"about_ca_system_score_codex":0.00026522498,"about_ca_system_score_gemma":0.0002278792,"threshold_uncertainty_score":0.00930357},"labels":[],"label_agreement":null},{"id":"W2092586481","doi":"10.1016/s0092-8674(01)00280-x","title":"Genomic Imprinting Disrupted by a Maternal Effect Mutation in the Dnmt1 Gene","year":2001,"lang":"en","type":"article","venue":"Cell","topic":"Genetic Syndromes and Imprinting","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":"McGill University; Montreal Children's Hospital","funders":"","keywords":"Biology; Genomic imprinting; Imprinting (psychology); Genetics; DNMT1; Gene; Mutation; DNA methylation; Gene expression","score_opus":0.004131198393370567,"score_gpt":0.21747506412499282,"score_spread":0.21334386573162226,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2092586481","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99117637,0.0010094292,0.0034347444,0.00038521554,0.00010046106,0.000020485506,0.0005424318,0.00032399365,0.0030068741],"genre_scores_gemma":[0.996933,0.00040415072,0.001144682,0.000034011508,0.000017521921,0.000009155452,0.000115789575,0.000028233768,0.0013135608],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99987686,0.000018165501,0.000014149412,0.000028212366,0.000042511496,0.000020070669],"domain_scores_gemma":[0.99972457,0.00008224685,0.00011011713,0.000021638212,0.000010207248,0.000051192765],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0000832734,0.00060460623,0.00029274725,0.0007365173,0.00025738383,0.00020098903,0.0002870196,0.00053245126,0.0021333862],"category_scores_gemma":[0.00047562437,0.00019761887,0.00020103062,0.0003133379,0.00060206145,0.00012734796,0.00033669898,0.00042986442,0.00028314194],"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":[0.00055044313,0.000038363534,0.00408452,0.00007981713,0.00006154293,0.027104836,0.00010634731,0.0005211556,0.95764965,0.002507507,0.00045221555,0.006843562],"study_design_scores_gemma":[0.00017292047,0.0003723811,0.04291498,0.000026727803,0.0002821806,0.096157104,0.00012045734,0.0022772246,0.8481008,0.000991968,0.008545303,0.00003799457],"about_ca_topic_score_codex":0.0017103618,"about_ca_topic_score_gemma":0.0016632172,"teacher_disagreement_score":0.0021333862,"about_ca_system_score_codex":0.0004750005,"about_ca_system_score_gemma":0.00035609386,"threshold_uncertainty_score":0.007136941},"labels":[],"label_agreement":null},{"id":"W2092668546","doi":"10.1038/nature00819","title":"Placental-specific IGF-II is a major modulator of placental and fetal growth","year":2002,"lang":"en","type":"article","venue":"Nature","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":1059,"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":"Biotechnology and Biological Sciences Research Council; Medical Research Council","keywords":"Placenta; Fetus; Biology; Genomic imprinting; Trophoblast; Imprinting (psychology); Fetal growth; Insulin-like growth factor 2; Endocrinology; Gene; Intrauterine growth restriction; Internal medicine; Andrology; Pregnancy; Gene expression; Genetics; Medicine; DNA methylation","score_opus":0.005329582875511895,"score_gpt":0.2037796558499418,"score_spread":0.1984500729744299,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2092668546","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.8646205,0.07956343,0.023839716,0.0013702831,0.00079019467,0.00007232963,0.0023290059,0.0006946243,0.026719784],"genre_scores_gemma":[0.98714954,0.005908913,0.0029857513,0.000114837116,0.00011670206,0.000020059899,0.0005508269,0.000041645424,0.0031117182],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9999238,0.000013039877,0.000004660623,0.000019843676,0.000023210849,0.00001544409],"domain_scores_gemma":[0.99985397,0.000036544592,0.000025779509,0.000011522297,0.00001948086,0.00005277851],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0001344172,0.0004793968,0.000260609,0.00049996306,0.00017792454,0.00043913472,0.0002891206,0.00023732168,0.0013057882],"category_scores_gemma":[0.00026552886,0.00020076819,0.0001119247,0.00022411102,0.0003677911,0.00019643776,0.00020974886,0.000429348,0.0002577758],"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":[0.00080487627,0.000021151665,0.003963795,0.00013202909,0.00002154777,0.0009329202,0.000047102287,0.00024379816,0.9624716,0.0015205479,0.0005278475,0.02931285],"study_design_scores_gemma":[0.00008846275,0.000498013,0.124392584,0.000050537838,0.00008034096,0.0042042476,0.00020692845,0.0011485062,0.83808565,0.0022677544,0.028936293,0.000040784143],"about_ca_topic_score_codex":0.0018422902,"about_ca_topic_score_gemma":0.0013606139,"teacher_disagreement_score":0.0018422902,"about_ca_system_score_codex":0.00060699054,"about_ca_system_score_gemma":0.00025795304,"threshold_uncertainty_score":0.0044040084},"labels":[],"label_agreement":null},{"id":"W2093861094","doi":"10.1111/j.1365-263x.2007.00857.x","title":"The oro‐dental phenotype in Prader–Willi syndrome: a survey of 15 patients","year":2007,"lang":"en","type":"article","venue":"International Journal of Paediatric Dentistry","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","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":"Hotel Dieu Hospital","funders":"","keywords":"Medicine; Short stature; Pediatrics; Body mass index; Oral hygiene; Overweight; Obesity; Dentistry; Internal medicine","score_opus":0.008752132501374299,"score_gpt":0.26953623670748156,"score_spread":0.26078410420610726,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2093861094","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99974734,0.00007341092,0.0000233221,0.0000067087944,8.0950326e-7,0.000004322634,0.00004089449,0.000001231704,0.00010191543],"genre_scores_gemma":[0.9995096,0.00016102144,0.00007272147,0.00001731601,0.000003362337,0.000009783406,0.00013181249,0.0000012142358,0.00009318087],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99962854,0.000067116285,0.000043688276,0.00010287372,0.000084761174,0.00007292863],"domain_scores_gemma":[0.999532,0.00008445285,0.00017022825,0.00001948549,0.00003956681,0.00015430788],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0002830283,0.00043806375,0.0003632078,0.0011207098,0.00041528075,0.00041149155,0.00026158284,0.0003915818,0.0014021251],"category_scores_gemma":[0.0011335112,0.00029717063,0.00022622742,0.00068227394,0.0004324923,0.00033449696,0.00049229147,0.00021522996,0.0002657449],"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":[0.0000658947,0.00004107756,0.9947529,0.000010706641,0.000017334381,0.0018619464,0.0003977442,0.000028379609,0.00064574415,0.000016816432,0.00006587812,0.0020956108],"study_design_scores_gemma":[0.000010883451,0.00033985256,0.98692685,0.000010939519,0.000020660547,0.011469773,0.0006999667,0.00007695654,0.00012674104,0.000021860254,0.0002888311,0.0000066593693],"about_ca_topic_score_codex":0.0020737515,"about_ca_topic_score_gemma":0.0016284264,"teacher_disagreement_score":0.0020737515,"about_ca_system_score_codex":0.0002197117,"about_ca_system_score_gemma":0.00022364824,"threshold_uncertainty_score":0.004690647},"labels":[],"label_agreement":null},{"id":"W2094145825","doi":"10.6000/2292-2598.2014.02.03.2","title":"Speech and Language Issues in Children with Prader-Willi Syndrome","year":2014,"lang":"en","type":"article","venue":"Journal of Intellectual Disability - Diagnosis and Treatment","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":0,"is_retracted":false,"has_abstract":true,"route_ca_aff":false,"route_ca_fund":false,"route_ca_venue":true,"route_about_ca":false,"ca_institutions":"","funders":"National Center for Research Resources; National Institutes of Health","keywords":"Apraxia; Language delay; Audiology; Language development; Language disorder; Medicine; Population; Psychology; Developmental psychology; Aphasia; Cognitive psychology; Cognition; Psychiatry","score_opus":0.009846461654526276,"score_gpt":0.2559011782236664,"score_spread":0.24605471656914016,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2094145825","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9989447,0.00033711595,0.000034290322,0.00010017942,0.000007491855,0.000010850034,0.000034546178,0.000007350769,0.0005234796],"genre_scores_gemma":[0.99929655,0.00031747032,0.00015619023,0.000061373576,0.000015288737,0.000013915828,0.000052796648,0.0000025013173,0.00008399413],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9993131,0.00015715313,0.00007755117,0.00010710526,0.00019287094,0.00015221725],"domain_scores_gemma":[0.9979206,0.0006509512,0.00092861964,0.000043378266,0.00013907041,0.00031747253],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0006657712,0.0005973516,0.00046826465,0.001762805,0.0010229669,0.00059458613,0.0003215242,0.0006649931,0.0018205019],"category_scores_gemma":[0.0044612843,0.00036795068,0.00025049658,0.0008010162,0.0013386435,0.00064573844,0.0007876611,0.00093009893,0.00024669836],"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":[0.00004467224,0.000051157178,0.96577036,0.000062226965,0.000012108996,0.027312094,0.002111024,0.000060035614,0.0010955174,0.00008838889,0.00034450658,0.0030478905],"study_design_scores_gemma":[0.00001308524,0.0003841965,0.8123127,0.000065940476,0.000030057428,0.18202499,0.0034953041,0.000120391276,0.00050556124,0.00014006191,0.0008920458,0.000015710617],"about_ca_topic_score_codex":0.0026165186,"about_ca_topic_score_gemma":0.0041632266,"teacher_disagreement_score":0.0026165186,"about_ca_system_score_codex":0.0005585755,"about_ca_system_score_gemma":0.0008365099,"threshold_uncertainty_score":0.006090224},"labels":[],"label_agreement":null},{"id":"W2094253962","doi":"10.1002/1098-2795(200007)56:3<345::aid-mrd3>3.0.co;2-1","title":"Monoalleleic transcription of the insulin-like growth factor-II gene (Igf2) in chick embryos","year":2000,"lang":"en","type":"article","venue":"Molecular Reproduction and Development","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","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":"University of Guelph","funders":"Natural Sciences and Engineering Research Council of Canada; Ontario Ministry of Agriculture, Food and Rural Affairs","keywords":"Biology; Genomic imprinting; Imprinting (psychology); Genetics; Allele; Gene; Insulin-like growth factor 2; Embryo; Gene expression; DNA methylation","score_opus":0.009029402656602696,"score_gpt":0.20395261244627477,"score_spread":0.19492320978967206,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2094253962","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99617565,0.00054692966,0.0017694718,0.000024657187,0.000009989242,0.000004181447,0.0004147807,0.000016845284,0.0010374935],"genre_scores_gemma":[0.99519914,0.0002600846,0.0010962813,0.000013840133,0.0000036376418,0.000007720485,0.0004647342,0.0000111236695,0.0029433782],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9999341,0.000005894607,0.00000406957,0.000029547335,0.000015622976,0.000010758312],"domain_scores_gemma":[0.99991727,0.000022275128,0.000015933838,0.000008677092,0.000010414219,0.000025381298],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.000055762117,0.00015825307,0.000089902904,0.00035774894,0.00014580027,0.00018111097,0.0000947823,0.00012009352,0.0010298284],"category_scores_gemma":[0.00012561306,0.00015810813,0.00009512519,0.000110472465,0.00018402832,0.00007407362,0.00013198999,0.00024292438,0.00030956574],"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":[0.00005951062,0.000001963179,0.0010922888,0.0000076742035,0.0000020571958,0.000067927685,0.000034161363,0.000018636303,0.99789184,0.00005570994,0.000013350088,0.0007549306],"study_design_scores_gemma":[0.000016430562,0.00019168235,0.25842792,0.000014460286,0.00002751155,0.0011033977,0.00014749801,0.0009528307,0.7362587,0.00012286943,0.0027263581,0.0000103914235],"about_ca_topic_score_codex":0.0027356655,"about_ca_topic_score_gemma":0.0047460534,"teacher_disagreement_score":0.0027356655,"about_ca_system_score_codex":0.00029177035,"about_ca_system_score_gemma":0.00012196309,"threshold_uncertainty_score":0.00543952},"labels":[],"label_agreement":null},{"id":"W2096270935","doi":"10.1111/cen.12694","title":"Growth hormone secretion decreases with age in paediatric <scp>P</scp>rader‐<scp>W</scp>illi syndrome","year":2014,"lang":"en","type":"article","venue":"Clinical Endocrinology","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":14,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":true,"ca_institutions":"SickKids Foundation; Hospital for Sick Children; University of Toronto","funders":"Hospital for Sick Children","keywords":"Medicine; Growth hormone deficiency; Internal medicine; Endocrinology; Bone age; Stimulation; Body mass index; Growth hormone; Pediatrics; Hormone","score_opus":0.017245802903601674,"score_gpt":0.2685242520589245,"score_spread":0.2512784491553228,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2096270935","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9990588,0.00047705165,0.000079756945,0.000024280896,0.0000034038083,0.0000036652345,0.00011547954,0.000006953748,0.00023054129],"genre_scores_gemma":[0.99926597,0.00036176635,0.0001424997,0.000011769237,0.000006522316,0.0000035828482,0.00013928674,0.0000022750871,0.00006622239],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9996979,0.000045347577,0.000042053438,0.000059568367,0.00009980116,0.000055406555],"domain_scores_gemma":[0.9981652,0.00025076713,0.0012952674,0.000034358323,0.00012899475,0.00012548912],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00036177694,0.00027729422,0.00025904312,0.0007965409,0.00016784757,0.0003317141,0.00020618526,0.0002681876,0.00093057496],"category_scores_gemma":[0.0030101745,0.00019061695,0.00018330084,0.00081967155,0.00035741655,0.00032539302,0.0002329932,0.00029637275,0.00017199905],"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":[0.000068110414,0.000007293976,0.99529135,0.000018103003,0.000008587629,0.0010168937,0.00011805384,0.000043747415,0.0011321544,0.0000128181855,0.00007612568,0.0022067341],"study_design_scores_gemma":[0.0000018269129,0.00007123664,0.99554116,0.0000063054317,0.0000061503915,0.0039135697,0.00006310927,0.000051210587,0.00023398036,0.0000063949133,0.00010343649,0.0000015438441],"about_ca_topic_score_codex":0.0033670238,"about_ca_topic_score_gemma":0.0029550593,"teacher_disagreement_score":0.0033670238,"about_ca_system_score_codex":0.00024497864,"about_ca_system_score_gemma":0.0003150435,"threshold_uncertainty_score":0.0066948533},"labels":[],"label_agreement":null},{"id":"W2096758563","doi":"10.1093/hmg/ddg067","title":"Beckwith-Wiedemann syndrome demonstrates a role for epigenetic control of normal development","year":2003,"lang":"en","type":"review","venue":"Human Molecular Genetics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":288,"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":"","keywords":"Genomic imprinting; Biology; Epigenetics; Imprinting (psychology); Genetics; Beckwith–Wiedemann syndrome; DNA methylation; Allele; Gene; Locus (genetics); Gene expression","score_opus":0.02191032540696159,"score_gpt":0.2867352236854542,"score_spread":0.2648248982784926,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2096758563","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":[0.000744347,0.99447614,0.00037191075,0.00028745175,0.00017875405,0.0000025180464,0.00001165716,0.000017521965,0.0039097206],"genre_scores_gemma":[0.0045901323,0.9926239,0.0005599675,0.00025422193,0.00012308058,0.0000050687304,0.00002365458,0.0000020979842,0.0018178667],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.9999248,0.00001423737,0.000009187097,0.000015338977,0.00002805175,0.000008454338],"domain_scores_gemma":[0.99993396,0.000030998046,0.000009959969,0.0000030659778,0.0000133787225,0.000008659339],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00016483534,0.00049710186,0.00064642355,0.0007614673,0.00015634763,0.00047405058,0.00036869984,0.00067712425,0.0019195371],"category_scores_gemma":[0.00025476632,0.000100998484,0.0001371858,0.0011351639,0.00035459825,0.0005951619,0.00032350587,0.0005330477,0.0016157996],"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":[0.000066784094,0.00002146287,0.00058627623,0.0040037604,0.000045881126,0.0017254531,0.00007936149,0.000177738,0.0056036604,0.004499783,0.012256514,0.97093326],"study_design_scores_gemma":[0.000012930612,0.00006606506,0.0029199894,0.0011131115,0.000059815182,0.012282834,0.00011464418,0.00004995592,0.0013289038,0.0023366131,0.9797028,0.000012400976],"about_ca_topic_score_codex":0.0006426319,"about_ca_topic_score_gemma":0.0011525118,"teacher_disagreement_score":0.0019195371,"about_ca_system_score_codex":0.00035298822,"about_ca_system_score_gemma":0.0004411049,"threshold_uncertainty_score":0.0064215064},"labels":[],"label_agreement":null},{"id":"W2096765959","doi":"10.1111/j.1399-0004.2007.00793.x","title":"Toward understanding the genetic basis of neural tube defects","year":2007,"lang":"en","type":"review","venue":"Clinical Genetics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","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":"McGill University; Université de Montréal; Centre Hospitalier Universitaire Sainte-Justine","funders":"","keywords":"Neural tube; Neurulation; Convergent extension; Biology; Neural tube defect; Genetics; Gene; Etiology; Bioinformatics; Pathology; Medicine; Embryogenesis; Embryo","score_opus":0.25823289677907457,"score_gpt":0.41922587509874265,"score_spread":0.16099297831966808,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2096765959","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":[0.00013551941,0.99752873,0.00039247988,0.00074031256,0.00030974057,0.000004155548,0.00001485822,0.000015145566,0.00085903076],"genre_scores_gemma":[0.00037349042,0.9982759,0.0004310931,0.0002621087,0.00023274642,0.0000050099916,0.000024197883,0.0000019291308,0.0003934984],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.9997726,0.000042212487,0.000033825716,0.00004099084,0.000091603346,0.000018672214],"domain_scores_gemma":[0.99950266,0.00023133476,0.000050580587,0.000021420314,0.00013722572,0.000056715573],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00084728235,0.0012033324,0.001503507,0.0024942434,0.00032388762,0.0010188193,0.0014282655,0.0019421893,0.003332517],"category_scores_gemma":[0.0010854726,0.00032135475,0.00046244686,0.0018950044,0.0010199677,0.0022766676,0.00080356543,0.0028235014,0.0028704829],"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":[0.00009728191,0.000073841096,0.00041412353,0.009513339,0.00009445203,0.0006445401,0.00007790335,0.0005602653,0.0030815636,0.008500972,0.042503186,0.9344384],"study_design_scores_gemma":[0.000027258971,0.00006424847,0.0011194866,0.0025657497,0.000092487266,0.002896085,0.00007341605,0.000111834386,0.0006348839,0.00433949,0.988054,0.000021095702],"about_ca_topic_score_codex":0.0013898126,"about_ca_topic_score_gemma":0.0014069397,"teacher_disagreement_score":0.003332517,"about_ca_system_score_codex":0.0010367853,"about_ca_system_score_gemma":0.0013028148,"threshold_uncertainty_score":0.011148393},"labels":[],"label_agreement":null},{"id":"W2097248205","doi":"10.1186/1471-2156-6-s1-s160","title":"A genome scan for parent-of-origin linkage effects in alcoholism","year":2005,"lang":"en","type":"article","venue":"BMC Genetics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":14,"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":"Canadian Institutes of Health Research; Genome Canada; Juvenile Diabetes Research Foundation International","keywords":"Genetics; Genetic linkage; Microsatellite; Imprinting (psychology); Biology; Genomic imprinting; Locus (genetics); SNP; Single-nucleotide polymorphism; Genome Scan; Linkage (software); Complete linkage; Tag SNP; Genome; Allele; Gene; Genotype; DNA methylation","score_opus":0.02355792446827854,"score_gpt":0.28590208020858654,"score_spread":0.262344155740308,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2097248205","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9962096,0.0004737702,0.0016990603,0.0002654031,0.00001109112,0.000015599411,0.0004478428,0.000042849948,0.000834821],"genre_scores_gemma":[0.99572796,0.00026043138,0.0029389425,0.00008967085,0.000018519862,0.000020630512,0.0006373651,0.000015457095,0.00029103135],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9993129,0.0002775024,0.000026773092,0.00017916715,0.00012733699,0.000076276716],"domain_scores_gemma":[0.9979802,0.0011792956,0.00035090122,0.000111816,0.00012921658,0.000248585],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0010852991,0.0003086216,0.0004282062,0.0014300817,0.00058820186,0.0003840672,0.00038664739,0.0006069457,0.0048973355],"category_scores_gemma":[0.002913408,0.00020029076,0.0005825515,0.001375739,0.00028978928,0.00018978183,0.00053453003,0.000644424,0.000198451],"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":[0.0020854783,0.00035026955,0.8813003,0.00021870292,0.002302671,0.003685918,0.0006749347,0.0010284805,0.06606663,0.0014083828,0.0021748731,0.038703445],"study_design_scores_gemma":[0.000065513574,0.0003371776,0.9915672,0.000019070721,0.00065583875,0.0028860471,0.000105836305,0.0008320238,0.0017442752,0.0005448353,0.0012308686,0.000011359262],"about_ca_topic_score_codex":0.0023496645,"about_ca_topic_score_gemma":0.0032874844,"teacher_disagreement_score":0.0048973355,"about_ca_system_score_codex":0.00016575279,"about_ca_system_score_gemma":0.0004113796,"threshold_uncertainty_score":0.016383171},"labels":[],"label_agreement":null},{"id":"W2098195823","doi":"10.1172/jci19159","title":"Autosomal dominant pseudohypoparathyroidism type Ib is associated with a heterozygous microdeletion that likely disrupts a putative imprinting control element of GNAS","year":2003,"lang":"en","type":"article","venue":"Journal of Clinical Investigation","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":259,"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; St. Michael's Hospital; McGill University","funders":"National Institute of Diabetes and Digestive and Kidney Diseases; Canadian Institutes of Health Research; U.S. Public Health Service; National Institutes of Health","keywords":"GNAS complex locus; Pseudohypoparathyroidism; Exon; Genetics; Genomic imprinting; Biology; Locus (genetics); X chromosome; Imprinting (psychology); X-inactivation; Differentially methylated regions; DNA methylation; Molecular biology; Gene; Parathyroid hormone; Internal medicine; Medicine","score_opus":0.038505553832486036,"score_gpt":0.3210772784450016,"score_spread":0.28257172461251556,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2098195823","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9988651,0.00019912295,0.00037034744,0.00001788052,0.0000042682027,0.000009838944,0.00008068899,0.000022916429,0.00042971116],"genre_scores_gemma":[0.9987876,0.00013383235,0.00046019204,0.000021996637,0.000011618904,0.00000895486,0.00017098396,0.000006389371,0.00039840167],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99984884,0.00001881726,0.000017996219,0.00004933954,0.0000362438,0.00002876605],"domain_scores_gemma":[0.9997192,0.000056318135,0.00012104678,0.000020114525,0.000013909505,0.00006931339],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.000068247115,0.00072401634,0.00028471331,0.00075826206,0.00037969372,0.00018349619,0.0003034877,0.00043813893,0.0017810176],"category_scores_gemma":[0.00044248623,0.0002660197,0.00021910336,0.00054215395,0.0004313078,0.00011350767,0.0003694003,0.00024192173,0.00025876123],"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":[0.0015989958,0.00020416827,0.4231416,0.0002508847,0.0003486531,0.12917867,0.0007830288,0.0002031918,0.41867533,0.0004879853,0.00058730406,0.024540171],"study_design_scores_gemma":[0.00008513054,0.00055995776,0.72587705,0.00001554237,0.00014810401,0.25852972,0.0001772218,0.00030313482,0.011885697,0.00018478712,0.0022152737,0.000018324989],"about_ca_topic_score_codex":0.001068343,"about_ca_topic_score_gemma":0.0016182123,"teacher_disagreement_score":0.0017810176,"about_ca_system_score_codex":0.00020162994,"about_ca_system_score_gemma":0.0001269602,"threshold_uncertainty_score":0.0059580803},"labels":[],"label_agreement":null},{"id":"W2099472522","doi":"10.1091/mbc.e15-01-0013","title":"Glycogen synthase kinase-3 (Gsk-3) plays a fundamental role in maintaining DNA methylation at imprinted loci in mouse embryonic stem cells","year":2015,"lang":"en","type":"article","venue":"Molecular Biology of the Cell","topic":"Genetic Syndromes and Imprinting","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":"McMaster University","funders":"National Institute on Aging","keywords":"Biology; GSK-3; Embryonic stem cell; DNA methylation; GSK3B; Glycogen synthase; Cell biology; Methylation; Genetics; Glycogen debranching enzyme; Kinase; DNA; Phosphorylation; Gene; Gene expression","score_opus":0.010876007822089542,"score_gpt":0.23565132364348265,"score_spread":0.2247753158213931,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2099472522","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9765621,0.0071623763,0.011904666,0.00010959517,0.000041850748,0.000023012852,0.0014219987,0.0004185755,0.0023558922],"genre_scores_gemma":[0.991215,0.0023604545,0.003534882,0.00006431598,0.0000097644925,0.000023870512,0.0010349969,0.000053479984,0.0017032095],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99988544,0.000009832945,0.000013557655,0.00003896694,0.000036372137,0.00001577521],"domain_scores_gemma":[0.9999049,0.0000096280055,0.000040167455,0.0000134506,0.000008379966,0.00002357682],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00013422764,0.00035496114,0.00022426278,0.00041690678,0.00016853669,0.0003043146,0.00018813023,0.00019197125,0.00075682503],"category_scores_gemma":[0.00014238067,0.00019777306,0.00036883904,0.00026098272,0.00028771412,0.00017179827,0.00038551266,0.00034840094,0.00040381766],"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":[0.000043462653,0.0000028570323,0.0017010716,0.00003712852,0.000010906806,0.000055507146,0.000013714214,0.00008005387,0.994836,0.00011181719,0.000031135827,0.003076482],"study_design_scores_gemma":[0.000014670705,0.00010853072,0.07640414,0.000020707761,0.00007011869,0.00048578018,0.000032485925,0.00093054475,0.91751146,0.00041585788,0.0039937915,0.000011984196],"about_ca_topic_score_codex":0.0008939932,"about_ca_topic_score_gemma":0.0016804705,"teacher_disagreement_score":0.0008939932,"about_ca_system_score_codex":0.00026375233,"about_ca_system_score_gemma":0.0002486003,"threshold_uncertainty_score":0.0025318265},"labels":[],"label_agreement":null},{"id":"W2099689315","doi":"10.1093/hmg/10.26.2989","title":"Tumor development in the Beckwith-Wiedemann syndrome is associated with a variety of constitutional molecular 11p15 alterations including imprinting defects of KCNQ1OT1","year":2001,"lang":"en","type":"article","venue":"Human Molecular Genetics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":246,"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","funders":"Hospital for Sick Children","keywords":"Imprinting (psychology); Genomic imprinting; Beckwith–Wiedemann syndrome; Biology; Wilms' tumor; Cancer research; Genetics; Uniparental disomy; DNA methylation; Gene; Chromosome; Karyotype; Gene expression","score_opus":0.02025831772675202,"score_gpt":0.25900953347926975,"score_spread":0.23875121575251773,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2099689315","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9987286,0.00040095087,0.0002768637,0.000009966213,0.0000028981601,0.0000045036027,0.000051691535,0.000010279154,0.0005142521],"genre_scores_gemma":[0.9994444,0.00017939284,0.00018643429,0.000006884691,0.0000023772443,0.0000027960234,0.00007051994,0.0000020361008,0.0001050684],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99977344,0.000036364076,0.000028074692,0.000061289895,0.000052162108,0.000048529448],"domain_scores_gemma":[0.99973375,0.00005886936,0.000101097896,0.000024588024,0.00001448048,0.00006712469],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00013637857,0.00027558347,0.00012568747,0.0008259262,0.00030000394,0.00021133655,0.000118473596,0.00016026532,0.0010449721],"category_scores_gemma":[0.00078337453,0.00019285224,0.00014186717,0.0004237908,0.00042543866,0.000110039306,0.00034292386,0.00012044147,0.000121273304],"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":[0.00025353304,0.000025558063,0.92636853,0.00006658746,0.00009417752,0.020066839,0.00036762128,0.00016902879,0.03764295,0.00034838097,0.00025280967,0.0143440785],"study_design_scores_gemma":[0.000017342389,0.00018397842,0.8645722,0.000021002728,0.000074624935,0.12506211,0.0001962426,0.00024495937,0.007999443,0.00014045052,0.0014771956,0.00001033798],"about_ca_topic_score_codex":0.0016321439,"about_ca_topic_score_gemma":0.0036584854,"teacher_disagreement_score":0.0016321439,"about_ca_system_score_codex":0.00016697614,"about_ca_system_score_gemma":0.00020893049,"threshold_uncertainty_score":0.0034957528},"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":"W2100135235","doi":"10.1093/hmg/ddm225","title":"Inactivation of the mouse Magel2 gene results in growth abnormalities similar to Prader-Willi syndrome","year":2007,"lang":"en","type":"article","venue":"Human Molecular Genetics","topic":"Genetic Syndromes and Imprinting","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 of Alberta","funders":"National Institute of Diabetes and Digestive and Kidney Diseases","keywords":"Biology; Failure to thrive; Phenotype; Circadian rhythm; Weaning; Endocrinology; Internal medicine; Obesity; Gene; Weight gain; Genetics; Mutation; Candidate gene; Body weight; Medicine","score_opus":0.012342074490906746,"score_gpt":0.24829184261847792,"score_spread":0.23594976812757118,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2100135235","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9910156,0.00076752465,0.0047054607,0.00014977422,0.000050631126,0.00003497987,0.0008237437,0.0003098783,0.002142319],"genre_scores_gemma":[0.9864807,0.00093043066,0.0045562442,0.000090320515,0.000028866847,0.00007299967,0.0013448326,0.000094521034,0.0064011086],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9998498,0.000021356145,0.000014618563,0.000046413148,0.00004744679,0.00002029962],"domain_scores_gemma":[0.99977094,0.00003379635,0.00009440018,0.000025771667,0.000008358493,0.00006681277],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0001280287,0.0005859299,0.00017854519,0.000606747,0.00013418618,0.00023242497,0.00027327813,0.0004210933,0.0020185278],"category_scores_gemma":[0.00021725257,0.00022340869,0.000307069,0.00020723636,0.00046824748,0.00017998493,0.0003583524,0.0005187681,0.0005740386],"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":[0.00012998575,0.00002819863,0.00071315095,0.000025919171,0.000012093095,0.0008231096,0.000016721799,0.00013647917,0.99604744,0.00049845106,0.0001180694,0.0014503096],"study_design_scores_gemma":[0.00014877318,0.0006500696,0.04452636,0.00002147936,0.0000865307,0.016001834,0.00006685688,0.0019552517,0.9241689,0.0006670197,0.011682638,0.00002440769],"about_ca_topic_score_codex":0.0003124037,"about_ca_topic_score_gemma":0.00068480667,"teacher_disagreement_score":0.0020185278,"about_ca_system_score_codex":0.0001949341,"about_ca_system_score_gemma":0.00016228734,"threshold_uncertainty_score":0.00675267},"labels":[],"label_agreement":null},{"id":"W2102400711","doi":"10.1093/hmg/ddg152","title":"Maternal alleles acquiring paternal methylation patterns in biparental complete hydatidiform moles","year":2003,"lang":"en","type":"article","venue":"Human Molecular Genetics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":139,"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":"McGill University Health Centre; McGill University","keywords":"Biology; Genomic imprinting; Offspring; Locus (genetics); Genetics; Allele; DNA methylation; Methylation; Imprinting (psychology); Gene; Epigenetics; Pregnancy; Gene expression","score_opus":0.021386487152126706,"score_gpt":0.26424906013302246,"score_spread":0.24286257298089575,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2102400711","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9991062,0.0001915745,0.00041956143,0.000009538423,0.0000021536773,0.000002020127,0.00007245362,0.000010177332,0.00018628253],"genre_scores_gemma":[0.9992304,0.00009951921,0.0003286564,0.00000723072,0.0000019936224,0.0000020978496,0.00008310361,0.000004300077,0.00024258877],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9998611,0.000018458037,0.000013013083,0.000039017268,0.00004110753,0.000027233718],"domain_scores_gemma":[0.99974185,0.00005156526,0.000104956234,0.000028688622,0.000021804392,0.00005104764],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.000091365306,0.00020505223,0.00021045763,0.00084098073,0.00016650285,0.0001621509,0.0001277626,0.00016051107,0.0012799284],"category_scores_gemma":[0.0005069217,0.00017507972,0.00012133577,0.0002793952,0.00018185176,0.0000788015,0.00029059744,0.00017547313,0.00015705122],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0006272095,0.000031189393,0.35874364,0.00006189196,0.00009397107,0.009115598,0.0009061244,0.00025823092,0.60686886,0.00022490107,0.00008826402,0.022980165],"study_design_scores_gemma":[0.000019127468,0.00022694696,0.908211,0.000009632674,0.00007246387,0.031051612,0.00018904347,0.00048245228,0.05811552,0.00020769356,0.001398179,0.000016401333],"about_ca_topic_score_codex":0.00091153785,"about_ca_topic_score_gemma":0.001164986,"teacher_disagreement_score":0.0012799284,"about_ca_system_score_codex":0.00012301416,"about_ca_system_score_gemma":0.000052063162,"threshold_uncertainty_score":0.0042817593},"labels":[],"label_agreement":null},{"id":"W2102431794","doi":"10.1186/1471-2164-12-204","title":"Recent acquisition of imprinting at the rodent Sfmbt2 locus correlates with insertion of a large block of miRNAs","year":2011,"lang":"en","type":"article","venue":"BMC Genomics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","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":"Mount Sinai Hospital; Toronto Zoo; Lunenfeld-Tanenbaum Research Institute; University of Guelph; University of Toronto","funders":"Medical Research Council; Natural Sciences and Engineering Research Council of Canada; Canadian Institutes of Health Research","keywords":"Genomic imprinting; Imprinting (psychology); Biology; Genetics; Gene; Locus (genetics); Allele; Gene expression; DNA methylation","score_opus":0.014791571845483863,"score_gpt":0.218131124595679,"score_spread":0.20333955275019513,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2102431794","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9981177,0.0003552414,0.00096746074,0.000024005863,0.0000042861716,0.0000030564536,0.00014748069,0.000059861723,0.00032098882],"genre_scores_gemma":[0.997459,0.00016119206,0.0010957257,0.000016802687,0.000008744196,0.000009202451,0.00053515757,0.000017689435,0.00069647894],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9999342,0.0000035002922,0.000005538697,0.000026948816,0.000015075668,0.000014842918],"domain_scores_gemma":[0.9996013,0.000045881185,0.00019992718,0.000034844332,0.000020514111,0.00009752876],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00008133103,0.00018972103,0.00013433301,0.0003379804,0.00010776814,0.00014770079,0.00016843578,0.0001522897,0.0013159948],"category_scores_gemma":[0.0002151239,0.00012663785,0.00017590249,0.0001746224,0.00021004365,0.000116200215,0.00016394375,0.0003482877,0.0002376799],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00019352017,0.000010780181,0.025466839,0.000034189692,0.000021165004,0.00039307028,0.000034040033,0.000058353857,0.97001207,0.000101014775,0.00005170802,0.00362322],"study_design_scores_gemma":[0.000026335396,0.0003006537,0.7712493,0.000010763537,0.00005933516,0.0057087634,0.0000455264,0.00048198752,0.2187062,0.00012399683,0.0032760056,0.000011091946],"about_ca_topic_score_codex":0.00049393094,"about_ca_topic_score_gemma":0.00085705175,"teacher_disagreement_score":0.0013159948,"about_ca_system_score_codex":0.00013351903,"about_ca_system_score_gemma":0.00012540052,"threshold_uncertainty_score":0.004402399},"labels":[],"label_agreement":null},{"id":"W2103059889","doi":"10.1093/hmg/ddn055","title":"Superovulation alters the expression of imprinted genes in the midgestation mouse placenta","year":2008,"lang":"en","type":"article","venue":"Human Molecular Genetics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":216,"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 Children's Hospital","funders":"University of Pennsylvania","keywords":"Genomic imprinting; Biology; Imprinting (psychology); Embryo; Epigenetics; Placenta; Embryogenesis; Andrology; Oocyte; DNA methylation; Genetics; Gene expression; Endocrinology; Gene; Fetus; Pregnancy","score_opus":0.020493465553971395,"score_gpt":0.2593692172811008,"score_spread":0.2388757517271294,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2103059889","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.996345,0.0013009616,0.0012150495,0.000053295258,0.0000141130995,0.000017708953,0.00027016798,0.000044249064,0.0007393721],"genre_scores_gemma":[0.99266833,0.0012321192,0.0012332054,0.000078316276,0.0000100128555,0.000043896525,0.00059503084,0.000058958638,0.004080121],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9998393,0.00002321739,0.00001557131,0.000037644804,0.000040049883,0.000044139186],"domain_scores_gemma":[0.99970955,0.00005061432,0.00011481449,0.000029335,0.000016012487,0.000079775404],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00013805502,0.00030117604,0.00023634371,0.0004727172,0.00012475895,0.00026749505,0.00023645393,0.00026481037,0.0013881855],"category_scores_gemma":[0.00018831276,0.00031136238,0.00033335347,0.00011773763,0.00026529783,0.00018162614,0.0004021571,0.00070240267,0.0002685527],"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":[0.000072029005,0.0000051613933,0.00018834122,0.00000669603,0.0000016509347,0.000045355533,0.000013464267,0.000010947332,0.99934036,0.000027348828,0.0000045138113,0.00028408345],"study_design_scores_gemma":[0.000017063334,0.0004264404,0.026617385,0.000008034547,0.000022710434,0.00039549818,0.00006507334,0.00032476624,0.9706745,0.00008015861,0.0013608832,0.000007559587],"about_ca_topic_score_codex":0.0009622836,"about_ca_topic_score_gemma":0.0010245099,"teacher_disagreement_score":0.0013881855,"about_ca_system_score_codex":0.00029882783,"about_ca_system_score_gemma":0.00020705661,"threshold_uncertainty_score":0.0046439767},"labels":[],"label_agreement":null},{"id":"W2103334703","doi":"10.1530/eje-10-0795","title":"Osteosclerosis in two brothers with autosomal dominant pseudohypoparathyroidism type 1b: bone histomorphometric analysis","year":2010,"lang":"en","type":"article","venue":"European Journal of Endocrinology","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":34,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Children's Hospital of Eastern Ontario","funders":"National Institute of Diabetes and Digestive and Kidney Diseases; Canadian Institutes of Health Research; Health Canada","keywords":"Pseudohypoparathyroidism; Internal medicine; Endocrinology; Osteosclerosis; Parathyroid hormone; Bone histomorphometry; Hyperphosphatemia; Bone mineral; Cortical bone; Chemistry; Osteoporosis; Medicine; Anatomy; Trabecular bone; Calcium; Pathology","score_opus":0.010484899791478283,"score_gpt":0.2412951619130499,"score_spread":0.2308102621215716,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2103334703","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9991229,0.00020559324,0.00019053476,0.000052621857,0.000011430897,0.000016132852,0.00009869478,0.000008221432,0.00029391347],"genre_scores_gemma":[0.99902225,0.000109987624,0.0003380309,0.00005605128,0.000017822042,0.000007723374,0.000110999215,0.000006856562,0.0003302127],"study_design_codex":"case_report","study_design_gemma":"observational","domain_scores_codex":[0.9993062,0.00007007593,0.00008445149,0.00020737304,0.00022751204,0.000104313],"domain_scores_gemma":[0.99918216,0.0001707855,0.00021655027,0.00005572455,0.000074362455,0.00030044076],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0004499277,0.0010032486,0.0007578199,0.0018257049,0.0010081356,0.0006917927,0.0005698343,0.001513576,0.0019238447],"category_scores_gemma":[0.0018659827,0.00091314124,0.0007599888,0.00062304677,0.0007696434,0.00043951662,0.0009773257,0.0008351237,0.00044720244],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00048574866,0.00038466192,0.43924832,0.00009174056,0.000087046305,0.52614105,0.0030211876,0.0001106326,0.025516992,0.00017267068,0.0002326609,0.004507203],"study_design_scores_gemma":[0.00004056964,0.0007052939,0.37958512,0.000022800281,0.000055211764,0.6158843,0.00083236233,0.00022811601,0.0018966616,0.00006451605,0.00066068233,0.000024351852],"about_ca_topic_score_codex":0.0030133186,"about_ca_topic_score_gemma":0.0037507836,"teacher_disagreement_score":0.0030133186,"about_ca_system_score_codex":0.0005740525,"about_ca_system_score_gemma":0.00035241005,"threshold_uncertainty_score":0.0064359307},"labels":[],"label_agreement":null},{"id":"W2103693713","doi":"10.1093/dnares/11.6.381","title":"An Evolutionary Scenaio for Genomic Imprinting of Impact Lying between Nonimprinted Neighbors","year":2004,"lang":"en","type":"article","venue":"DNA Research","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":11,"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; Japan Society for the Promotion of Science; Ministry of Education, Culture, Sports, Science and Technology","keywords":"Genomic imprinting; Imprinting (psychology); Biology; Gene; Genetics; Gene duplication; Operon; Genome; DNA methylation; Gene expression","score_opus":0.0555185238834559,"score_gpt":0.396038315595073,"score_spread":0.3405197917116171,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2103693713","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9847164,0.0018819197,0.008622323,0.00021067285,0.000022617758,0.0000075370276,0.00010940284,0.00008279696,0.004346322],"genre_scores_gemma":[0.9946837,0.0007959999,0.0021701532,0.00007112832,0.000019706278,0.0000066589446,0.00015237108,0.000018310553,0.0020821106],"study_design_codex":"bench_or_experimental","study_design_gemma":"theoretical_or_conceptual","domain_scores_codex":[0.9998567,0.0000164816,0.0000058382743,0.000053580152,0.000037381615,0.000029967274],"domain_scores_gemma":[0.99978906,0.00005401909,0.000058998965,0.00003143396,0.00001362521,0.000052914933],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00017791367,0.00019837401,0.00020263618,0.00059887936,0.00027192896,0.00036734363,0.0003265939,0.00028703024,0.0015641117],"category_scores_gemma":[0.0002169551,0.00016016219,0.00021802285,0.0002388346,0.0005574001,0.00035341704,0.00050059514,0.0004250215,0.0002277567],"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":[0.00023442128,0.000010190587,0.013652604,0.000043119366,0.000017374628,0.0012465983,0.00015159875,0.0002264494,0.96792084,0.004859171,0.000056391586,0.011581069],"study_design_scores_gemma":[0.00009838061,0.001080776,0.3512109,0.00006136572,0.0002226931,0.016880294,0.0008484721,0.0028362505,0.594086,0.009445003,0.023152908,0.00007696544],"about_ca_topic_score_codex":0.00019781209,"about_ca_topic_score_gemma":0.0005194368,"teacher_disagreement_score":0.0015641117,"about_ca_system_score_codex":0.00025587197,"about_ca_system_score_gemma":0.00017616418,"threshold_uncertainty_score":0.005232513},"labels":[],"label_agreement":null},{"id":"W2103889681","doi":"10.1097/01.asn.0000023431.16173.55","title":"Renal Abnormalities in Beckwith-Wiedemann Syndrome Are Associated with 11p15.5 Uniparental Disomy","year":2002,"lang":"en","type":"article","venue":"Journal of the American Society of Nephrology","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":68,"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","funders":"National Cancer Institute","keywords":"Beckwith–Wiedemann syndrome; Uniparental disomy; Imprinting (psychology); Genomic imprinting; Medicine; Gigantism; Incidence (geometry); Macroglossia; Internal medicine; Gastroenterology; Pathology; Biology; Genetics; Gene; Chromosome; Karyotype","score_opus":0.012176448068181151,"score_gpt":0.22168039189991876,"score_spread":0.2095039438317376,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2103889681","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99851173,0.00057107187,0.00024378957,0.000027109463,0.000006437361,0.0000064293176,0.0000663344,0.000011662315,0.000555523],"genre_scores_gemma":[0.99921584,0.00030576697,0.0002907624,0.000027310029,0.000014295798,0.000003672494,0.000067600515,0.0000025115414,0.00007218616],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9996383,0.000055114095,0.00005543893,0.000080491416,0.000086653985,0.00008399184],"domain_scores_gemma":[0.9994728,0.00011856315,0.00024151614,0.000030415607,0.000022826558,0.000113885435],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0002133236,0.00042330872,0.00028683932,0.00088487356,0.0004215731,0.00032058972,0.00019552959,0.00034968852,0.0011315483],"category_scores_gemma":[0.0013337396,0.00034748606,0.00020401338,0.0007835575,0.0005465319,0.00025798698,0.0004624318,0.00027782266,0.00021743204],"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":[0.00018823994,0.000031659092,0.9200386,0.00005030291,0.00005310169,0.06328343,0.0003096722,0.000091271584,0.0075647645,0.00020414921,0.00027381332,0.007910993],"study_design_scores_gemma":[0.000021125612,0.00013235,0.7074242,0.00002499651,0.0000688267,0.28967276,0.00019319408,0.00015482095,0.0013623887,0.00017914333,0.00074696826,0.000019123298],"about_ca_topic_score_codex":0.0011484923,"about_ca_topic_score_gemma":0.0015900211,"teacher_disagreement_score":0.0011484923,"about_ca_system_score_codex":0.00016592183,"about_ca_system_score_gemma":0.0002122052,"threshold_uncertainty_score":0.0037853718},"labels":[],"label_agreement":null},{"id":"W2105964357","doi":"10.1111/j.1365-2788.2007.01004.x","title":"Facial expression of affect in children with Cornelia de Lange syndrome","year":2007,"lang":"en","type":"article","venue":"Journal of Intellectual Disability Research","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":27,"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":"Cornelia de Lange Syndrome; Affect (linguistics); Psychology; Facial expression; Developmental psychology; Medicine; Pediatrics; Communication","score_opus":0.036131907131039524,"score_gpt":0.3464480980124535,"score_spread":0.310316190881414,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2105964357","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9997546,0.00004042452,0.00003197681,0.0000074858112,0.0000014560787,0.0000033516028,0.000017327971,0.0000017494489,0.00014157541],"genre_scores_gemma":[0.99974865,0.000058596168,0.00010346444,0.000006927892,0.0000017057018,0.0000068660115,0.000024634537,0.0000010163243,0.000048196584],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99937207,0.0001160608,0.000053882464,0.00010228976,0.00022460984,0.00013113752],"domain_scores_gemma":[0.9990614,0.00025436413,0.00043092796,0.000038603364,0.00008015374,0.0001346447],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0005059986,0.0005289483,0.000444183,0.0010468449,0.00045163103,0.0003989525,0.00017978357,0.00032680228,0.0008398027],"category_scores_gemma":[0.00242268,0.0001687887,0.00027538493,0.0005534236,0.0008871315,0.0002404353,0.00054727815,0.0004174656,0.000087494154],"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":[0.00041896888,0.00011856902,0.96882564,0.000061552055,0.000037503887,0.008403466,0.0028334353,0.00017109995,0.010501178,0.00007735325,0.00015200973,0.008399299],"study_design_scores_gemma":[0.000013599319,0.00034255718,0.98148465,0.000009199513,0.000025811943,0.01580323,0.001263452,0.00009741753,0.0007644869,0.00003485348,0.00015070733,0.000009978418],"about_ca_topic_score_codex":0.0032751097,"about_ca_topic_score_gemma":0.0034575628,"teacher_disagreement_score":0.0032751097,"about_ca_system_score_codex":0.00062265765,"about_ca_system_score_gemma":0.00026960688,"threshold_uncertainty_score":0.006512046},"labels":[],"label_agreement":null},{"id":"W2108321118","doi":"10.14740/jem.v4i4.235","title":"Pseudopseudohypoparathyroidism With a Novel Mutation in the GNAS Gene Showing Thin Bones of Extremities and Ossification of Entheses","year":2014,"lang":"en","type":"article","venue":"Journal of Endocrinology and Metabolism","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":0,"is_retracted":false,"has_abstract":true,"route_ca_aff":false,"route_ca_fund":false,"route_ca_venue":true,"route_about_ca":false,"ca_institutions":"","funders":"","keywords":"GNAS complex locus; Medicine; Exon; Ossification; Enthesis; Gene; Endocrinology; Internal medicine; Genetics; Molecular biology; Anatomy; Biology","score_opus":0.017841005248087634,"score_gpt":0.24206418267447108,"score_spread":0.22422317742638345,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2108321118","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.95910835,0.005638804,0.007323975,0.015083194,0.0039443546,0.00010611257,0.0006530789,0.0005926414,0.007549573],"genre_scores_gemma":[0.98503137,0.001831019,0.0045476872,0.0013675087,0.0014477398,0.00004111017,0.00020883659,0.00011313833,0.0054114778],"study_design_codex":"case_report","study_design_gemma":"case_report","domain_scores_codex":[0.99944276,0.000047230813,0.00008797149,0.00018262831,0.00013683095,0.000102694146],"domain_scores_gemma":[0.9986571,0.0005907079,0.00031715707,0.00008819557,0.00010863811,0.00023813326],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0003228653,0.0013449827,0.0010422098,0.0018413608,0.0008370557,0.0008103105,0.0012060576,0.004391571,0.005689504],"category_scores_gemma":[0.002781421,0.00084826583,0.0011000014,0.0012138314,0.0015974256,0.0011815351,0.0009543875,0.00254336,0.000934361],"study_design_candidate":"case_report","study_design_consensus":"case_report","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.000057243014,0.000009013095,0.0010988239,0.000037327896,0.000013130408,0.99162275,0.00007694813,0.000049816997,0.005199657,0.00027979352,0.0006436174,0.00091185],"study_design_scores_gemma":[0.000027846034,0.000028831599,0.0031373806,0.000011111025,0.000029350527,0.991852,0.00004380161,0.00025862688,0.0029891622,0.0002623204,0.0013421566,0.0000174212],"about_ca_topic_score_codex":0.0016209639,"about_ca_topic_score_gemma":0.0012859489,"teacher_disagreement_score":0.005689504,"about_ca_system_score_codex":0.0009491945,"about_ca_system_score_gemma":0.0006149028,"threshold_uncertainty_score":0.019033253},"labels":[],"label_agreement":null},{"id":"W2108580735","doi":"10.1016/j.metabol.2014.11.011","title":"Hormonal and Metabolic Responses to Endurance Exercise in Children With Prader–Willi Syndrome and Non-Syndromic Obesity","year":2014,"lang":"en","type":"article","venue":"Metabolism","topic":"Genetic Syndromes and Imprinting","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 Alberta","funders":"Canadian Institutes of Health Research","keywords":"Endocrinology; Internal medicine; Medicine; Hormone; Epinephrine; Endocrine system; Obesity; Lean body mass; Body weight","score_opus":0.004455833042478412,"score_gpt":0.20419753078619973,"score_spread":0.19974169774372133,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2108580735","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9993943,0.00012664672,0.000029948045,0.000035336485,0.000006007348,0.0000037541004,0.00010919213,0.0000037612172,0.00029100355],"genre_scores_gemma":[0.9996278,0.0000885382,0.000043000993,0.000019298679,0.000008438232,0.000005776439,0.00010569898,0.0000023205005,0.000098973],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99974924,0.00006306613,0.000026014508,0.000052261727,0.00004599255,0.000063479594],"domain_scores_gemma":[0.99933726,0.00026646903,0.00016074453,0.000028154172,0.00003546204,0.00017191625],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0002162715,0.0005118569,0.00046534475,0.0007643026,0.00029034985,0.00033525936,0.00029162018,0.00040141484,0.0012479936],"category_scores_gemma":[0.0019103521,0.0002500296,0.00038938367,0.0006570973,0.00048744804,0.00022692,0.00034098933,0.0007319127,0.00011235007],"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":[0.0009786016,0.00023791463,0.9832183,0.000037764992,0.00006349962,0.0064674374,0.0004893223,0.00023950613,0.005007447,0.00004426465,0.00009828309,0.0031176761],"study_design_scores_gemma":[0.000011455364,0.00028995762,0.99515945,0.000003428455,0.0000303595,0.0035754382,0.00032725034,0.000112347036,0.00037630522,0.000019447245,0.00008912395,0.00000539892],"about_ca_topic_score_codex":0.004832445,"about_ca_topic_score_gemma":0.0037909425,"teacher_disagreement_score":0.004832445,"about_ca_system_score_codex":0.00032287516,"about_ca_system_score_gemma":0.00025628263,"threshold_uncertainty_score":0.009608626},"labels":[],"label_agreement":null},{"id":"W2108618113","doi":"10.1210/jc.2004-1848","title":"Hypermethylation of the Promoter Region Is Associated with the Loss of <i>MEG3</i> Gene Expression in Human Pituitary Tumors","year":2005,"lang":"en","type":"article","venue":"The Journal of Clinical Endocrinology & Metabolism","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":209,"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; U.S. Public Health Service; National Institutes of Health; National Institute of Mental Health; Jarislowsky Foundation; Massachusetts General Hospital","keywords":"MEG3; DNA methylation; Biology; Pituitary tumors; Carcinogenesis; Gene expression; Genomic imprinting; Methylation; Cancer research; Gene isoform; Gene; Molecular biology; RNA; Endocrinology; Genetics; Long non-coding RNA","score_opus":0.025862963179958134,"score_gpt":0.3079542497951875,"score_spread":0.28209128661522936,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2108618113","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99791735,0.0006527319,0.000734799,0.00005307227,0.0000059708805,0.0000052882524,0.00017732917,0.000038545077,0.00041495683],"genre_scores_gemma":[0.998566,0.00031601108,0.00036414442,0.000022755617,0.000007985847,0.000004926159,0.00029078595,0.000009585367,0.00041778776],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.99989164,0.000015636413,0.000008823014,0.000037882535,0.000029158391,0.000016857437],"domain_scores_gemma":[0.99977225,0.00005260797,0.0000970991,0.000018548999,0.000017512268,0.000041905587],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00008928069,0.00020618526,0.00019366099,0.00033663958,0.00015860748,0.00017381126,0.00010265683,0.00019004222,0.0012859679],"category_scores_gemma":[0.00028526652,0.00015245503,0.00012701155,0.00019892122,0.00027034612,0.000082566265,0.0001544498,0.00027665863,0.00025379536],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00027459467,0.000015127773,0.011690558,0.000037403803,0.000020268852,0.0010743338,0.00008170778,0.000053689164,0.98359734,0.00008141431,0.00007259537,0.0030009223],"study_design_scores_gemma":[0.000053900803,0.00049089926,0.4409874,0.000015308362,0.00013080203,0.023706084,0.00019330456,0.0006772547,0.5302459,0.0004733061,0.003005689,0.000020170937],"about_ca_topic_score_codex":0.0010291194,"about_ca_topic_score_gemma":0.0011459613,"teacher_disagreement_score":0.0012859679,"about_ca_system_score_codex":0.00019896918,"about_ca_system_score_gemma":0.0001808823,"threshold_uncertainty_score":0.004302025},"labels":[],"label_agreement":null},{"id":"W2108691006","doi":"10.1098/rsbl.2007.0189","title":"Virgin birth in a hammerhead shark","year":2007,"lang":"en","type":"article","venue":"Biology Letters","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":179,"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":"Queen's University Belfast; Florida Sea Grant, University of Florida; Queen's University; Wildlife Conservation Society; National Science Foundation","keywords":"Chondrichthyes; Biology; Parthenogenesis; Vertebrate; Elasmobranchii; Zoology; Facultative; Evolutionary biology; Ecology; Fishery; Embryo; Genetics; Gene","score_opus":0.008765734897021621,"score_gpt":0.25125457054088657,"score_spread":0.24248883564386495,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2108691006","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99956733,0.000024020104,0.000051583454,0.000015606616,0.000004916266,0.000001626183,0.00001972498,0.000008162941,0.000307103],"genre_scores_gemma":[0.99817777,0.000035731406,0.00009406155,0.00001737773,0.0000035131256,0.000001690091,0.000040794446,0.0000030168492,0.001626072],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.99993646,0.0000056710405,0.000005179807,0.000018490822,0.000013059568,0.000021085969],"domain_scores_gemma":[0.9998331,0.000026796304,0.000038682363,0.000020408059,0.000010912412,0.0000699083],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00011483128,0.00014195865,0.00017657704,0.000487895,0.00052824017,0.00019286144,0.0002650354,0.00025862904,0.0022096531],"category_scores_gemma":[0.00026176646,0.0001560624,0.0001736837,0.00012276809,0.00054897275,0.00010661618,0.00045691527,0.00030944182,0.00030720487],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0016594136,0.00060426677,0.29977104,0.000084443614,0.000062724386,0.057967443,0.0022570102,0.0007036099,0.5972973,0.0015452686,0.00080167316,0.03724575],"study_design_scores_gemma":[0.00005295356,0.002776143,0.9268035,0.000011950995,0.00005981416,0.033607397,0.0012570127,0.00067263853,0.0324161,0.00036783112,0.001927333,0.00004731202],"about_ca_topic_score_codex":0.0029537207,"about_ca_topic_score_gemma":0.0046141995,"teacher_disagreement_score":0.0029537207,"about_ca_system_score_codex":0.00035382883,"about_ca_system_score_gemma":0.00021852752,"threshold_uncertainty_score":0.007392049},"labels":[],"label_agreement":null},{"id":"W2109753113","doi":"10.1002/0471695998.mgs010","title":"<scp>B</scp>eckwith‐<scp>W</scp>iedemann Syndrome and Hemihyperplasia","year":2005,"lang":"en","type":"other","venue":"","topic":"Genetic Syndromes and Imprinting","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":"SickKids Foundation; Hospital for Sick Children; University of Toronto","funders":"","keywords":"Macroglossia; Beckwith–Wiedemann syndrome; Medicine; Duodenal atresia; Polyhydramnios; Population; Incidence (geometry); Pediatrics; Endocrinology; Internal medicine; Biology; Genetics; Pathology; Pregnancy; Fetus; Gene; Tongue; Atresia","score_opus":0.006385053581246507,"score_gpt":0.22008321788003476,"score_spread":0.21369816429878827,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2109753113","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.7387461,0.0052010496,0.0042552925,0.0021449686,0.0002830435,0.00010496854,0.0014929761,0.00029561465,0.24747601],"genre_scores_gemma":[0.94476277,0.0015076536,0.003380609,0.00046170887,0.00016049831,0.000042022413,0.0011298256,0.000058989495,0.048495956],"study_design_codex":"case_report","study_design_gemma":"case_report","domain_scores_codex":[0.9999144,0.0000138833,0.000008211757,0.000015177691,0.00002420434,0.000024085524],"domain_scores_gemma":[0.999821,0.000031807453,0.00004384671,0.00001528081,0.000020530599,0.00006755101],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00015506189,0.0006733798,0.00017342834,0.00096781267,0.00031579618,0.00041857178,0.0002565491,0.00044673678,0.019647388],"category_scores_gemma":[0.00037957556,0.00008705481,0.00014253389,0.00043907863,0.0003717037,0.00025237532,0.00041848922,0.00037209172,0.0019265834],"study_design_candidate":"case_report","study_design_consensus":"case_report","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0013336429,0.00041110735,0.15943429,0.00043919185,0.00019666992,0.49783155,0.00029854907,0.0007342426,0.1002592,0.0313385,0.03934222,0.16838089],"study_design_scores_gemma":[0.00014652748,0.00017740786,0.16607073,0.0002003162,0.000112923335,0.6981685,0.00028869387,0.0012918956,0.02399913,0.006825891,0.102684565,0.00003339781],"about_ca_topic_score_codex":0.0016619009,"about_ca_topic_score_gemma":0.0018718704,"teacher_disagreement_score":0.019647388,"about_ca_system_score_codex":0.00023780526,"about_ca_system_score_gemma":0.0002506122,"threshold_uncertainty_score":0.065727055},"labels":[],"label_agreement":null},{"id":"W2110063687","doi":"10.1038/jhg.2014.30","title":"The imprinted gene LRRTM1 mediates schizotypy and handedness in a nonclinical population","year":2014,"lang":"en","type":"article","venue":"Journal of Human Genetics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":49,"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; Simon Fraser University","funders":"","keywords":"Single-nucleotide polymorphism; Epigenetics; Genetics; Schizotypy; Allele; DNA methylation; Biology; Schizophrenia (object-oriented programming); Genomic imprinting; Population; SNP; Genetic variation; Gene; Psychology; Genotype; Gene expression; Cognition; Neuroscience; Medicine; Psychiatry","score_opus":0.01173395077742766,"score_gpt":0.28492919129464983,"score_spread":0.27319524051722216,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2110063687","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99963164,0.000019002833,0.000058639005,0.00002657864,0.0000019808867,0.000002931511,0.000026616104,0.0000023224597,0.0002302313],"genre_scores_gemma":[0.9994386,0.000034141627,0.00006158905,0.000020393334,0.0000066150856,0.000004111256,0.000055609667,0.00000688318,0.00037198095],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9995894,0.00013691826,0.000032224554,0.00009680454,0.00007597645,0.00006866061],"domain_scores_gemma":[0.99921596,0.00032051167,0.00018170929,0.000066101216,0.000070394985,0.00014530602],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00041029902,0.0009886594,0.00042593858,0.0011591613,0.0015047982,0.00074232183,0.00048085817,0.0004759321,0.0041831695],"category_scores_gemma":[0.0022461603,0.0003538226,0.00025329157,0.00059191,0.0011038292,0.00035509857,0.0005610302,0.0006019667,0.00045914177],"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":[0.0015991261,0.00051596825,0.9277723,0.000024785186,0.00008960072,0.012249209,0.004779311,0.00011577416,0.04505386,0.00058537547,0.00036281423,0.006851935],"study_design_scores_gemma":[0.00008187842,0.0006165481,0.978024,0.00001438509,0.00007224691,0.015251428,0.0023294105,0.0006195689,0.002057446,0.0005334334,0.00037658092,0.00002293351],"about_ca_topic_score_codex":0.004105055,"about_ca_topic_score_gemma":0.0038300776,"teacher_disagreement_score":0.0041831695,"about_ca_system_score_codex":0.00024788504,"about_ca_system_score_gemma":0.0003037679,"threshold_uncertainty_score":0.013994098},"labels":[],"label_agreement":null},{"id":"W2111319296","doi":"10.1093/jmcb/mjq029","title":"Genome-wide Gene Expression Profiling Reveals Aberrant MAPK and Wnt Signaling Pathways Associated with Early Parthenogenesis","year":2010,"lang":"en","type":"article","venue":"Journal of Molecular Cell Biology","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":42,"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":"College of Medicine, University of Florida; Moffitt Cancer Center; University of South Florida; Cancer Research Institute","keywords":"Biology; Wnt signaling pathway; Gene expression; Parthenogenesis; Embryo; Signal transduction; MAPK/ERK pathway; Gene expression profiling; Gene; Regulation of gene expression; Genomic imprinting; Cell biology; Genetics; DNA methylation","score_opus":0.008691608230164138,"score_gpt":0.20422749012950772,"score_spread":0.1955358818993436,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2111319296","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.996274,0.0012497777,0.0009695818,0.000025146926,0.000003129781,0.000011743436,0.0010980605,0.000026332198,0.00034230427],"genre_scores_gemma":[0.9913119,0.0014276325,0.001737586,0.000062403065,0.000005135473,0.000048620415,0.0035962404,0.000015616111,0.0017949353],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.99991286,0.000008531245,0.0000058165215,0.000031468837,0.000022829227,0.000018432744],"domain_scores_gemma":[0.99992824,0.00001230089,0.000030444446,0.0000060376283,0.0000073005226,0.00001576489],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00009127997,0.00022723523,0.0003571793,0.00039090056,0.0001326672,0.0002591684,0.000100229685,0.00021471077,0.00051103206],"category_scores_gemma":[0.00010642806,0.00014819865,0.0002704276,0.00045366568,0.00013589191,0.000085157815,0.00013715426,0.00025885302,0.00014332969],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00013302453,0.000007635791,0.0046712887,0.00002691184,0.000016814694,0.00008524057,0.00001748897,0.000047298057,0.9936946,0.000016127951,0.000026633184,0.0012568363],"study_design_scores_gemma":[0.000016061193,0.00019516422,0.79846936,0.0000067042397,0.00009460027,0.0010786918,0.00007200454,0.00077099714,0.19772394,0.000064544205,0.0014962442,0.000011800176],"about_ca_topic_score_codex":0.000542147,"about_ca_topic_score_gemma":0.000814745,"teacher_disagreement_score":0.000542147,"about_ca_system_score_codex":0.00011091811,"about_ca_system_score_gemma":0.00011643948,"threshold_uncertainty_score":0.0017095208},"labels":[],"label_agreement":null},{"id":"W2111787288","doi":"10.1002/ajmg.c.30268","title":"Imprinted genes and human disease","year":2010,"lang":"en","type":"editorial","venue":"American Journal of Medical Genetics Part C Seminars in Medical Genetics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":34,"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; Hospital for Sick Children","funders":"","keywords":"Imprinting (psychology); Genomic imprinting; Human genome; Disease; Phenotype; Biology; Human genetics; Human disease; Computational biology; Genetics; DNA microarray; Gene; Medical genetics; Bioinformatics; Genome; Medicine; Pathology; Gene expression","score_opus":0.006013900462875183,"score_gpt":0.2991589590729615,"score_spread":0.2931450586100863,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2111787288","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":[0.00006698334,0.027116055,0.0001187876,0.039690465,0.9315438,0.000011185524,0.000031411026,0.000045846435,0.0013753879],"genre_scores_gemma":[0.0005551989,0.021151967,0.00013237029,0.020776078,0.9501944,0.000014171732,0.00003051944,0.000022905535,0.00712234],"study_design_codex":"not_applicable","study_design_gemma":"not_applicable","domain_scores_codex":[0.99869066,0.00026893197,0.00016875796,0.00016885504,0.00059973454,0.000102999446],"domain_scores_gemma":[0.9935915,0.0031692658,0.00037155848,0.00017803894,0.0015654875,0.0011241564],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0029527955,0.0030173785,0.0025236402,0.0018367391,0.0012346185,0.0033811536,0.002588133,0.0076576197,0.00922265],"category_scores_gemma":[0.0076009147,0.00064786087,0.0012244339,0.00087028946,0.001879911,0.002739583,0.0011957649,0.012609872,0.007293322],"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":[0.0000420704,0.000013601819,0.000043181826,0.000215044,0.000012544834,0.0001364881,0.000019176334,0.000021942667,0.00009282586,0.00043607276,0.9870837,0.01188337],"study_design_scores_gemma":[0.000056233737,0.00004045963,0.0003410939,0.00037134503,0.000033138153,0.000586499,0.000034816036,0.00009730849,0.00011935739,0.0013855144,0.99692243,0.000011808508],"about_ca_topic_score_codex":0.0006347649,"about_ca_topic_score_gemma":0.0016857248,"teacher_disagreement_score":0.00922265,"about_ca_system_score_codex":0.0016432585,"about_ca_system_score_gemma":0.0014303931,"threshold_uncertainty_score":0.030852854},"labels":[],"label_agreement":null},{"id":"W2111879149","doi":"10.1186/1756-8935-4-10","title":"Genome-wide mapping of imprinted differentially methylated regions by DNA methylation profiling of human placentas from triploidies","year":2011,"lang":"en","type":"article","venue":"Epigenetics & Chromatin","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":81,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Child and Family Research Institute; University of British Columbia","funders":"","keywords":"Genomic imprinting; Differentially methylated regions; Biology; Imprinting (psychology); DNA methylation; Epigenetics; Genetics; Methylation; Gene; GNAS complex locus; Gene expression","score_opus":0.025998162810465554,"score_gpt":0.24634956916660475,"score_spread":0.2203514063561392,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2111879149","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9981304,0.0005438669,0.00078369805,0.000012439338,0.0000010622072,0.00000477139,0.00036259557,0.000008147359,0.00015306522],"genre_scores_gemma":[0.99832815,0.00030818043,0.00058763946,0.000011611457,0.0000015534193,0.000008098074,0.00056086614,0.0000046258992,0.00018937855],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9999237,0.000009040395,0.000006674085,0.00003171887,0.000016305907,0.00001246787],"domain_scores_gemma":[0.99984,0.000043962777,0.0000598172,0.000017579385,0.000015353891,0.000023150147],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00014209488,0.000120164426,0.0001838042,0.0008915667,0.00011861106,0.0002209735,0.0001129946,0.00015015477,0.0006777082],"category_scores_gemma":[0.0003760509,0.0001181024,0.00016710389,0.000488398,0.00015461646,0.00008753004,0.00031145086,0.00014396606,0.000082305196],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00081428426,0.0000128897955,0.1294723,0.000097943244,0.00013783736,0.00038982456,0.00034442698,0.00021456703,0.85874933,0.000072912175,0.00005939799,0.00963439],"study_design_scores_gemma":[0.000018107556,0.00015707106,0.95343596,0.000007844943,0.00012328353,0.0019320918,0.0001846689,0.00083372125,0.04221406,0.00010712562,0.0009779303,0.00000802279],"about_ca_topic_score_codex":0.0011766842,"about_ca_topic_score_gemma":0.0011793813,"teacher_disagreement_score":0.0011766842,"about_ca_system_score_codex":0.00015216079,"about_ca_system_score_gemma":0.000072953684,"threshold_uncertainty_score":0.0023396015},"labels":[],"label_agreement":null},{"id":"W2112006955","doi":"10.1186/s13039-015-0109-8","title":"Functional consequences of copy number variants in miscarriage","year":2015,"lang":"en","type":"article","venue":"Molecular Cytogenetics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":24,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Child and Family Research Institute; University of British Columbia","funders":"Institute of Genetics; Canadian Institutes of Health Research; Michael Smith Health Research BC","keywords":"Miscarriage; Genomic imprinting; Recurrent miscarriage; Biology; Copy-number variation; Gene duplication; Gene; Genetics; Human genetics; Gene expression; Pregnancy; DNA methylation; Genome","score_opus":0.028357092811402026,"score_gpt":0.2660852716924739,"score_spread":0.2377281788810719,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2112006955","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99475694,0.0022125826,0.0014870437,0.00008063264,0.000020550373,0.000007942893,0.00064747746,0.000050258495,0.00073664536],"genre_scores_gemma":[0.99865663,0.00031191725,0.00054362044,0.000017567821,0.000013311368,0.0000063572456,0.00024920632,0.000013453978,0.00018785264],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9993186,0.00013191205,0.00006578305,0.0002276314,0.00018597719,0.00007015871],"domain_scores_gemma":[0.99758315,0.0011448612,0.00074841705,0.00016760534,0.00016278254,0.00019321653],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00053213595,0.00033775766,0.00030343275,0.0018593974,0.00025584782,0.0004557836,0.00042101688,0.00047137224,0.0036216888],"category_scores_gemma":[0.0033999276,0.00010754876,0.00028759043,0.00092935347,0.00045067823,0.00019943912,0.0003797156,0.00028772317,0.00026782093],"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":[0.002227024,0.00006276894,0.64665294,0.0003560867,0.0005152447,0.012503095,0.0006277747,0.000905984,0.29457757,0.0009613039,0.00041793688,0.04019235],"study_design_scores_gemma":[0.000026637063,0.0003361438,0.91567594,0.000054348726,0.00042666678,0.03895647,0.000215195,0.0015969989,0.038664065,0.0013981835,0.0026145407,0.0000348357],"about_ca_topic_score_codex":0.0006197536,"about_ca_topic_score_gemma":0.0004123478,"teacher_disagreement_score":0.0036216888,"about_ca_system_score_codex":0.00027121307,"about_ca_system_score_gemma":0.00012442512,"threshold_uncertainty_score":0.012115777},"labels":[],"label_agreement":null},{"id":"W2112806377","doi":"10.1038/4541054a","title":"Battle of the sexes may set the brain","year":2008,"lang":"en","type":"article","venue":"Nature","topic":"Genetic Syndromes and Imprinting","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":"Simon Fraser University","funders":"","keywords":"DISC1; Autism; Schizophrenia (object-oriented programming); Offspring; Genomic imprinting; Battle; Mental illness; Biology; Genetics; Gene; Psychology; Neuroscience; Psychiatry; Mental health; History; Gene expression; DNA methylation; Pregnancy","score_opus":0.007808402554892995,"score_gpt":0.2430938038181333,"score_spread":0.23528540126324032,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2112806377","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.47675413,0.097065896,0.035351355,0.21237715,0.010243624,0.000040162493,0.0009808631,0.000964453,0.16622233],"genre_scores_gemma":[0.9500359,0.014124523,0.0056385435,0.010207888,0.0011115075,0.000017894157,0.0000962886,0.00009115525,0.018676292],"study_design_codex":"theoretical_or_conceptual","study_design_gemma":"observational","domain_scores_codex":[0.99974376,0.00007885321,0.0000095582645,0.000043402844,0.00005846437,0.0000659243],"domain_scores_gemma":[0.9996087,0.00012371542,0.000055257347,0.000051086958,0.00003838978,0.00012283698],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0006663653,0.00032786987,0.00040927686,0.0004173261,0.0010619937,0.002337081,0.0005806407,0.0016604996,0.0044225273],"category_scores_gemma":[0.0012398461,0.00022062214,0.00021347436,0.00024170821,0.004693224,0.0032070973,0.00089424837,0.0018328024,0.00064247363],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0007298289,0.000041275085,0.0065349946,0.00012720523,0.00011498305,0.0025082547,0.0008448105,0.0009720695,0.06260795,0.84852445,0.018214876,0.05877929],"study_design_scores_gemma":[0.00008862022,0.00013620408,0.0122736925,0.00008781943,0.00007054896,0.0027621666,0.0021023108,0.0008821585,0.031967867,0.75299793,0.19652937,0.0001013538],"about_ca_topic_score_codex":0.0010879366,"about_ca_topic_score_gemma":0.002963526,"teacher_disagreement_score":0.0044225273,"about_ca_system_score_codex":0.0010685724,"about_ca_system_score_gemma":0.00090415595,"threshold_uncertainty_score":0.014794767},"labels":[],"label_agreement":null},{"id":"W2114100575","doi":"10.1093/hmg/ddm280","title":"Manipulations of mouse embryos prior to implantation result in aberrant expression of imprinted genes on day 9.5 of development","year":2007,"lang":"en","type":"article","venue":"Human Molecular Genetics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":321,"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":"Eunice Kennedy Shriver National Institute of Child Health and Human Development; National Institute of General Medical Sciences; McGill University","keywords":"Genomic imprinting; Biology; Embryo; Imprinting (psychology); Yolk sac; Allele; Genetics; Embryogenesis; Gene expression; Locus (genetics); Gene; Andrology; DNA methylation","score_opus":0.01972676159889489,"score_gpt":0.28773413457619784,"score_spread":0.2680073729773029,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2114100575","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9877082,0.0024253733,0.0061042095,0.00010662898,0.000084551495,0.00009438952,0.0010010063,0.0001337718,0.0023418076],"genre_scores_gemma":[0.9794486,0.0028573957,0.008417063,0.00011172144,0.000023474971,0.00022218187,0.0016075189,0.00007641131,0.0072355294],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99972063,0.000045497403,0.00003632098,0.000071838156,0.00007539632,0.00005021668],"domain_scores_gemma":[0.99978286,0.000059456906,0.00007636981,0.000033734057,0.000013195212,0.000034316567],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0002165038,0.00042748614,0.00023239969,0.00029851633,0.00017887338,0.00032204692,0.00029740672,0.00035390473,0.001643602],"category_scores_gemma":[0.00019000273,0.00025953806,0.0003256646,0.000117033014,0.00026291827,0.00017589108,0.00026721339,0.0008044147,0.0005594056],"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":[0.00003952431,0.0000087468725,0.00013511584,0.000011026913,0.0000023605194,0.000045152778,0.00001026173,0.000011341791,0.9993518,0.000029725428,0.000009606652,0.00034524055],"study_design_scores_gemma":[0.000007037131,0.00022004337,0.004918239,0.0000061576297,0.0000130668695,0.00020474964,0.000018079822,0.0001151383,0.9929141,0.000021672997,0.0015581829,0.000003564327],"about_ca_topic_score_codex":0.00049624825,"about_ca_topic_score_gemma":0.0010310275,"teacher_disagreement_score":0.001643602,"about_ca_system_score_codex":0.00025228653,"about_ca_system_score_gemma":0.00017577875,"threshold_uncertainty_score":0.0054984093},"labels":[],"label_agreement":null},{"id":"W2114234140","doi":"10.1590/s1807-59322009000100008","title":"Sonographic Assessment of Renal Growth in Patients with Beckwith-Wiedemann Syndrome: The Beckwith-Wiedemann Syndrome Renal Nomogram","year":2009,"lang":"en","type":"article","venue":"Clinics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","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":"Alberta Children's Hospital","funders":"","keywords":"Beckwith–Wiedemann syndrome; Medicine; Nomogram; Kidney; Kidney disease; Supine position; Nephrectomy; Internal medicine; Urology; Pediatrics","score_opus":0.007847839787356698,"score_gpt":0.25937647578878575,"score_spread":0.25152863600142905,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2114234140","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9980167,0.00033529702,0.00087131857,0.000043955817,0.0000065462973,0.000024525812,0.00015590127,0.000015576552,0.00053016824],"genre_scores_gemma":[0.99704236,0.00018985516,0.0023733696,0.000014098675,0.000012082005,0.000039450235,0.00027020602,0.0000036828394,0.000054839176],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9994679,0.00021313701,0.00009739158,0.000056430894,0.00012477164,0.00004049823],"domain_scores_gemma":[0.9974285,0.000987886,0.0009358902,0.00008795359,0.00026379296,0.00029596116],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0013948007,0.00050907524,0.0004170332,0.0019694637,0.00026219306,0.0005032207,0.00029947242,0.0003496647,0.00079080474],"category_scores_gemma":[0.0050107264,0.00017974498,0.0003215711,0.0008419794,0.0003405048,0.0005628923,0.0005365116,0.00034607179,0.00018173197],"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":[0.00010868837,0.000008095282,0.9970945,0.000007062879,0.000012194184,0.00018022393,0.000028892617,0.00012536242,0.00036156335,0.000013206336,0.0000509993,0.0020091701],"study_design_scores_gemma":[0.000021247943,0.00028869478,0.9922504,0.000015060971,0.000045182718,0.004647504,0.00020990157,0.0017167035,0.00049008953,0.000043520806,0.00026060018,0.000010998485],"about_ca_topic_score_codex":0.00081746373,"about_ca_topic_score_gemma":0.0010378057,"teacher_disagreement_score":0.0019694637,"about_ca_system_score_codex":0.00021783501,"about_ca_system_score_gemma":0.0002590636,"threshold_uncertainty_score":0.0073764324},"labels":[],"label_agreement":null},{"id":"W2114728169","doi":"10.1101/gr.111922.110","title":"A novel approach identifies new differentially methylated regions (DMRs) associated with imprinted genes","year":2011,"lang":"en","type":"article","venue":"Genome Research","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":139,"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; Institute for Clinical Evaluative Sciences; Lunenfeld-Tanenbaum Research Institute; Mount Sinai Hospital; Hospital for Sick Children; Public Health Ontario; University of Toronto","funders":"National Institute of General Medical Sciences; Canadian Institutes of Health Research; National Institutes of Health; Hospital for Sick Children; Ministério da Ciência, Tecnologia e Ensino Superior; GlaxoSmithKline; University of Toronto; Fundação para a Ciência e a Tecnologia; McGill University","keywords":"Biology; Differentially methylated regions; Genetics; Genomic imprinting; Gene; DNA methylation; Computational biology; Gene expression","score_opus":0.11435360814045456,"score_gpt":0.31099517195343557,"score_spread":0.196641563812981,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2114728169","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.84228045,0.006719786,0.139004,0.00077445566,0.00012227811,0.00033549333,0.004909221,0.00090161926,0.004952734],"genre_scores_gemma":[0.754882,0.0031645838,0.22934853,0.0005905991,0.000063040985,0.00020774332,0.0056764386,0.00008837743,0.005978727],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9997981,0.000015039054,0.000009270534,0.000092663664,0.00005506443,0.000029819359],"domain_scores_gemma":[0.99982697,0.000042218246,0.00004471894,0.000027174674,0.000020835982,0.000038075374],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00022567008,0.00044409238,0.00046619505,0.0011291584,0.00025566103,0.0003968836,0.0004141483,0.00046273894,0.0016213021],"category_scores_gemma":[0.0003955518,0.00024524785,0.00039134294,0.00042789016,0.00024049883,0.0002519937,0.00050721,0.00061136566,0.0004910509],"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":[0.00013475968,0.000028108312,0.0034792437,0.00011101396,0.000047517562,0.00018587473,0.000033905228,0.0001346646,0.97641164,0.00028184615,0.00015697216,0.018994436],"study_design_scores_gemma":[0.00013949073,0.0006466356,0.075590245,0.00003600846,0.00029916485,0.008108959,0.00010805665,0.0077424226,0.88026744,0.0010174374,0.025988957,0.000055189204],"about_ca_topic_score_codex":0.0009130564,"about_ca_topic_score_gemma":0.0038612704,"teacher_disagreement_score":0.0016213021,"about_ca_system_score_codex":0.00030407825,"about_ca_system_score_gemma":0.00032193246,"threshold_uncertainty_score":0.0054237843},"labels":[],"label_agreement":null},{"id":"W2115095020","doi":"10.1093/hmg/ddm281","title":"Coordinated diurnal regulation of genes from the Dlk1–Dio3 imprinted domain: implications for regulation of clusters of non-paralogous genes","year":2007,"lang":"en","type":"article","venue":"Human Molecular Genetics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":28,"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; Douglas Mental Health University Institute; McGill University","funders":"Eunice Kennedy Shriver National Institute of Child Health and Human Development; National Institute of Diabetes and Digestive and Kidney Diseases; Canadian Institutes of Health Research; National Institutes of Health; McGill University","keywords":"Congenic; Enhancer; Biology; Genomic imprinting; Gene; Genetics; Imprinting (psychology); Regulation of gene expression; Genome; Regulator; Chromosome; Regulatory sequence; Gene expression; DNA methylation","score_opus":0.014073947542418244,"score_gpt":0.2748342011835551,"score_spread":0.26076025364113686,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2115095020","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9965917,0.00057518773,0.0020247363,0.000044537523,0.0000091361835,0.0000058797073,0.000283857,0.000041364943,0.00042369234],"genre_scores_gemma":[0.99544,0.00028658292,0.0019767254,0.00005235513,0.0000059838812,0.000017687906,0.0005321858,0.00003352982,0.0016549483],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9999045,0.000008637484,0.0000063227603,0.000040075643,0.00001720387,0.000023329303],"domain_scores_gemma":[0.9997931,0.000025643303,0.00008221484,0.00002172497,0.000013259834,0.00006405879],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00009171579,0.0002259599,0.00015744887,0.0001998884,0.000101044236,0.00021515058,0.00019334051,0.00013569187,0.00076367863],"category_scores_gemma":[0.00009283034,0.000115988994,0.00017593235,0.00010490088,0.00023179622,0.00014745047,0.00023186057,0.00032603115,0.00013821757],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.000048213442,0.0000033097276,0.0006414924,0.0000066619596,0.0000010250056,0.00001574086,0.000008735077,0.000011761126,0.9988726,0.000026113164,0.00000401283,0.00036035085],"study_design_scores_gemma":[0.000020935271,0.00011913238,0.2106711,0.000009133688,0.000020080503,0.00033317035,0.00009676901,0.00089073094,0.7864761,0.00013339866,0.001217418,0.000012068086],"about_ca_topic_score_codex":0.00059987674,"about_ca_topic_score_gemma":0.0015651077,"teacher_disagreement_score":0.00076367863,"about_ca_system_score_codex":0.0002645706,"about_ca_system_score_gemma":0.00012590831,"threshold_uncertainty_score":0.0025547743},"labels":[],"label_agreement":null},{"id":"W2115123766","doi":"10.1002/ppul.10152","title":"Sleep and breathing in Prader‐Willi syndrome","year":2002,"lang":"en","type":"review","venue":"Pediatric Pulmonology","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":214,"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 Children's Hospital","funders":"","keywords":"Medicine; Polysomnography; Obstructive sleep apnea; Pediatrics; Non-rapid eye movement sleep; Hypoventilation; Hypotonia; Sleep apnea; Abnormality; Excessive daytime sleepiness; Apnea; Sleep disorder; Anesthesia; Internal medicine; Insomnia; Respiratory system; Psychiatry; Electroencephalography","score_opus":0.02104118724063914,"score_gpt":0.2674210782155739,"score_spread":0.2463798909749348,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2115123766","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":[0.0003061124,0.9962081,0.00024213611,0.00044474954,0.00055224856,0.000006296209,0.000015033577,0.000015530377,0.0022097642],"genre_scores_gemma":[0.0018734833,0.99530053,0.00027473443,0.0002994803,0.000528315,0.000007049734,0.000042281466,0.0000024592255,0.0016716252],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.9998554,0.000027060441,0.000021029058,0.000025135674,0.000055394576,0.00001592866],"domain_scores_gemma":[0.9998099,0.000081028855,0.000030092193,0.0000084925405,0.000044607605,0.000025974263],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00035428535,0.0012732823,0.0015334046,0.0021746308,0.00036194804,0.0007080474,0.0010470792,0.001461279,0.0031976083],"category_scores_gemma":[0.00067957473,0.00026204437,0.00035967323,0.0017645202,0.00061836647,0.0012136376,0.00050726195,0.0014628655,0.0032340798],"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":[0.00008449905,0.00007660107,0.0006331914,0.0065628304,0.00006570608,0.0029629332,0.00008031674,0.0003966291,0.0011687076,0.0020718852,0.04525661,0.94064003],"study_design_scores_gemma":[0.000049409715,0.000081750186,0.0028689762,0.002432798,0.000109253604,0.027675131,0.000117946685,0.00011581684,0.00043354323,0.0024792575,0.9636102,0.000025965253],"about_ca_topic_score_codex":0.0013443923,"about_ca_topic_score_gemma":0.0020183471,"teacher_disagreement_score":0.0031976083,"about_ca_system_score_codex":0.0006246209,"about_ca_system_score_gemma":0.00080121926,"threshold_uncertainty_score":0.010697067},"labels":[],"label_agreement":null},{"id":"W2115328346","doi":"10.1002/1096-8628(20010801)102:2<161::aid-ajmg1453>3.0.co;2-o","title":"GPC3 mutation analysis in a spectrum of patients with overgrowth expands the phenotype of Simpson-Golabi-Behmel syndrome","year":2001,"lang":"en","type":"article","venue":"American Journal of Medical Genetics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":129,"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; Children's & Women's Health Centre of British Columbia; Hospital for Sick Children; University of British Columbia; SickKids Foundation; University of Toronto","funders":"","keywords":"Sotos syndrome; Hepatoblastoma; Genetics; Gigantism; Beckwith–Wiedemann syndrome; Exon; Biology; Medicine; Gene; Internal medicine","score_opus":0.0035735619762140244,"score_gpt":0.2290597276600335,"score_spread":0.22548616568381946,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2115328346","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9995828,0.00006858745,0.000077461,0.000013121152,0.0000011445536,0.0000025853988,0.000028034108,0.0000051508578,0.00022100934],"genre_scores_gemma":[0.9997311,0.000040339964,0.00011200621,0.00001652093,0.0000027907668,0.0000018961265,0.00004748226,0.0000024840017,0.000045392957],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99985254,0.000018271774,0.000017875458,0.00004377314,0.000037810813,0.000029788238],"domain_scores_gemma":[0.99982125,0.00006123474,0.00003168962,0.000011155027,0.000018172115,0.00005651349],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00012723362,0.0004919551,0.00023423361,0.0009297287,0.00037851447,0.00025350202,0.00012591959,0.0003275259,0.00087223336],"category_scores_gemma":[0.000706178,0.00018416664,0.00019659234,0.00040293133,0.00039241437,0.00012894599,0.000325282,0.00018982164,0.00013379788],"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":[0.0005450196,0.000070451206,0.7447919,0.000044813638,0.00007153786,0.10881307,0.0013647213,0.00042648762,0.13079415,0.00023470436,0.00036194446,0.012481132],"study_design_scores_gemma":[0.000061766885,0.00033766843,0.7846466,0.000019904634,0.000075555196,0.20451881,0.00039671164,0.0010843622,0.0077165556,0.00019677458,0.00092776504,0.000017499182],"about_ca_topic_score_codex":0.0013105914,"about_ca_topic_score_gemma":0.001155871,"teacher_disagreement_score":0.0013105914,"about_ca_system_score_codex":0.00016724879,"about_ca_system_score_gemma":0.00011899476,"threshold_uncertainty_score":0.0029178858},"labels":[],"label_agreement":null},{"id":"W2116283958","doi":"10.1002/ajmg.a.31074","title":"Angelman syndrome 2005: Updated consensus for diagnostic criteria","year":2006,"lang":"en","type":"article","venue":"American Journal of Medical Genetics Part A","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":646,"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; McMaster Children's Hospital","funders":"","keywords":"Statement (logic); Consensus conference; Angelman syndrome; Scientific consensus; Salient; Scientific evidence; Management science; MEDLINE; Scientific literature; Computer science; Psychology; Medical physics; Medicine; Political science; Artificial intelligence; Epistemology; Engineering; Library science; Law","score_opus":0.00980346440927048,"score_gpt":0.2805707475976675,"score_spread":0.270767283188397,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2116283958","genre_codex":"review","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":[0.0121147465,0.4462733,0.16220248,0.24269049,0.061109953,0.0048504514,0.013756327,0.0023504288,0.054651797],"genre_scores_gemma":[0.061997574,0.20127706,0.6085189,0.032792445,0.011384724,0.007963553,0.055943377,0.000989153,0.019133136],"study_design_codex":"not_applicable","study_design_gemma":"not_applicable","domain_scores_codex":[0.9769455,0.0071792034,0.007472905,0.0012067179,0.0060675307,0.0011280925],"domain_scores_gemma":[0.9440995,0.010039156,0.0044178376,0.0014638647,0.037188377,0.002791306],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.045898214,0.0022397137,0.0042061745,0.017058425,0.0019382215,0.0039950325,0.010222998,0.006874027,0.0028211703],"category_scores_gemma":[0.06354504,0.0012047907,0.0040712026,0.008339832,0.0025551368,0.0036017662,0.004456951,0.008808102,0.0032754585],"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":[0.00020471326,0.00013148399,0.006579258,0.0041556065,0.0002867497,0.0016144122,0.00082643476,0.0018248992,0.0012572659,0.01267827,0.6177425,0.35269836],"study_design_scores_gemma":[0.00029630394,0.00014541531,0.018975379,0.015619692,0.0006030011,0.011515756,0.0012168753,0.0024789667,0.0017093822,0.020750316,0.92638993,0.00029902428],"about_ca_topic_score_codex":0.016879126,"about_ca_topic_score_gemma":0.016795801,"teacher_disagreement_score":0.045898214,"about_ca_system_score_codex":0.0076174927,"about_ca_system_score_gemma":0.02138941,"threshold_uncertainty_score":0.24273586},"labels":[],"label_agreement":null},{"id":"W2116673901","doi":"10.1530/eje.0.1470561","title":"Parental genomic imprinting in endocrinopathies","year":2002,"lang":"en","type":"review","venue":"European Journal of Endocrinology","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":28,"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":"Genomic imprinting; Imprinting (psychology); Nesidioblastosis; Endocrinology; Internal medicine; Pseudohypoparathyroidism; Biology; Gene; Genetics; Uniparental disomy; Diabetes mellitus; Medicine; DNA methylation; Gene expression; Parathyroid hormone; Chromosome; Karyotype; Islet","score_opus":0.034659856889521126,"score_gpt":0.2815494556447907,"score_spread":0.2468895987552696,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2116673901","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":[0.0002685567,0.9968273,0.00032856592,0.00020133678,0.00026135767,0.0000028966872,0.000010544302,0.00001161434,0.0020878306],"genre_scores_gemma":[0.0015543747,0.9965162,0.00025426745,0.0001160086,0.00022308843,0.000004108749,0.00001871643,0.0000015907659,0.0013115613],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.9998857,0.000023557104,0.000013355411,0.000024285471,0.000041965173,0.000011153694],"domain_scores_gemma":[0.999838,0.00007243454,0.000021637428,0.000007633263,0.000040413706,0.00001985049],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00042933592,0.0008161363,0.001257525,0.0011810191,0.00026844494,0.00080415333,0.0007982061,0.0010579877,0.0026835597],"category_scores_gemma":[0.00050368306,0.00021222138,0.00019741604,0.0019294848,0.00044636984,0.000848415,0.0004892649,0.0008577556,0.0026840512],"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":[0.00007157174,0.000037611495,0.0003230312,0.0049052606,0.000040065686,0.0011079716,0.000058967147,0.00036863858,0.0023518545,0.0034618487,0.01933761,0.9679356],"study_design_scores_gemma":[0.000024124824,0.000067530294,0.0016048542,0.0013595098,0.000084820225,0.0068288776,0.0000969158,0.00009393741,0.0011028335,0.0035226126,0.985194,0.000019925475],"about_ca_topic_score_codex":0.0008946523,"about_ca_topic_score_gemma":0.0015261656,"teacher_disagreement_score":0.0026835597,"about_ca_system_score_codex":0.00054461934,"about_ca_system_score_gemma":0.00057832955,"threshold_uncertainty_score":0.008977354},"labels":[],"label_agreement":null},{"id":"W2116972945","doi":"10.1002/ajmg.a.35358","title":"Brain abnormalities in patients with Beckwith–Wiedemann syndrome","year":2012,"lang":"en","type":"article","venue":"American Journal of Medical Genetics Part A","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":42,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Credit Valley Hospital; Hospital for Sick Children; University of Toronto; SickKids Foundation; Mount Sinai Hospital","funders":"","keywords":"Beckwith–Wiedemann syndrome; Dysgenesis; Genomic imprinting; Corpus callosum; Microdeletion syndrome; Genetics; Abnormality; Global developmental delay; Biology; Phenotype; Bioinformatics; Pathology; Medicine; Gene; Neuroscience; DNA methylation","score_opus":0.0063699365381236816,"score_gpt":0.2407267676707134,"score_spread":0.23435683113258973,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2116972945","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9971289,0.00070200535,0.00023755556,0.00010864984,0.000020217174,0.000011478888,0.00012932422,0.00003400755,0.0016278424],"genre_scores_gemma":[0.9990404,0.0003714792,0.00027989878,0.000060052644,0.000023938854,0.0000071529957,0.00012845901,0.000004439021,0.00008404478],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99976665,0.000034826975,0.000035663754,0.00006257238,0.00005477772,0.000045493336],"domain_scores_gemma":[0.9996767,0.00007991816,0.00012459459,0.000018788007,0.000022911025,0.00007704044],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00015195824,0.0008158759,0.00040194843,0.0014450358,0.0006102278,0.00044816305,0.0002440801,0.00058250927,0.0013235228],"category_scores_gemma":[0.0012962753,0.00029383833,0.00021587098,0.0008789662,0.0005340831,0.0003360565,0.0004908155,0.00041364663,0.00019585967],"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":[0.0002824887,0.000067610716,0.83792895,0.000056761804,0.0000856678,0.13858214,0.0006277952,0.00019136822,0.0096588,0.00030483856,0.0007272294,0.011486382],"study_design_scores_gemma":[0.000035651166,0.00026396665,0.56592226,0.00004647993,0.000105024315,0.42912105,0.00050023204,0.00035449714,0.0016910702,0.00051660184,0.0014055087,0.000037600876],"about_ca_topic_score_codex":0.0013922919,"about_ca_topic_score_gemma":0.0015996934,"teacher_disagreement_score":0.0014450358,"about_ca_system_score_codex":0.00021926699,"about_ca_system_score_gemma":0.00030402723,"threshold_uncertainty_score":0.004427612},"labels":[],"label_agreement":null},{"id":"W2117121254","doi":"10.1093/hmg/11.11.1317","title":"Discordant KCNQ1OT1 imprinting in sets of monozygotic twins discordant for Beckwith-Wiedemann syndrome","year":2002,"lang":"en","type":"article","venue":"Human Molecular Genetics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":332,"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","funders":"Division of Materials Research; National Cancer Institute","keywords":"Beckwith–Wiedemann syndrome; Imprinting (psychology); Biology; Genomic imprinting; Genetics; Monozygotic twin; DNA methylation; Gene","score_opus":0.022097774345631992,"score_gpt":0.26649348897152436,"score_spread":0.24439571462589238,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2117121254","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9994481,0.000100146295,0.00009482168,0.000006609782,0.000004170642,0.000004276963,0.000049576673,0.0000027107767,0.00028945974],"genre_scores_gemma":[0.99959785,0.0000469606,0.00014268847,0.000009265557,0.000003003422,0.0000041495,0.00010606094,0.000004112162,0.00008591534],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9991202,0.0001369762,0.00014770558,0.0002484971,0.00022560524,0.00012110539],"domain_scores_gemma":[0.99917406,0.00018754299,0.0002801138,0.000119354954,0.00006790103,0.00017096043],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00026925522,0.00035378683,0.00054763193,0.0020783986,0.00085465296,0.00048578263,0.0004091505,0.00036911655,0.0011852628],"category_scores_gemma":[0.0023898534,0.00046060217,0.00039500298,0.00067645474,0.0006375937,0.00013759505,0.0008747086,0.00023767585,0.00017966326],"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":[0.0020222336,0.00012046927,0.78606164,0.000093126066,0.00033511332,0.020897973,0.0034865008,0.000261317,0.17826219,0.0006071919,0.00023535169,0.0076167937],"study_design_scores_gemma":[0.000036414494,0.00024028182,0.9082965,0.000026990027,0.00015675717,0.07377763,0.0008400632,0.0005468651,0.014987913,0.00029737444,0.00075845676,0.000034759287],"about_ca_topic_score_codex":0.001692583,"about_ca_topic_score_gemma":0.0022347972,"teacher_disagreement_score":0.0020783986,"about_ca_system_score_codex":0.00030303147,"about_ca_system_score_gemma":0.00018844496,"threshold_uncertainty_score":0.0039651394},"labels":[],"label_agreement":null},{"id":"W2117476997","doi":"10.1111/j.1399-0004.2010.01547.x","title":"CCMG guidelines: prenatal and postnatal diagnostic testing for uniparental disomy","year":2010,"lang":"en","type":"article","venue":"Clinical Genetics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":65,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":true,"ca_institutions":"London Health Sciences Centre; McMaster University; Victoria General Hospital; Montreal Children's Hospital; Children's Hospital of Eastern Ontario; Alberta Children's Hospital; Diagnostic Services Manitoba","funders":"","keywords":"Uniparental disomy; Genetic testing; Prenatal diagnosis; Guideline; Medicine; Diagnostic test; Genetic counseling; Medical genetics; Genetics; Family medicine; Pediatrics; Biology; Pregnancy; Chromosome; Karyotype; Pathology","score_opus":0.06582523456584276,"score_gpt":0.3774007015368377,"score_spread":0.3115754669709949,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2117476997","genre_codex":"commentary","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":[0.008446154,0.0995345,0.03473802,0.5712658,0.030378014,0.0062040123,0.02617102,0.0028161074,0.2204464],"genre_scores_gemma":[0.05806028,0.12310886,0.28302354,0.31859237,0.01259627,0.00848907,0.054120876,0.0012216317,0.14078712],"study_design_codex":"not_applicable","study_design_gemma":"not_applicable","domain_scores_codex":[0.99115443,0.0023626683,0.0017707975,0.00033379564,0.0037383358,0.00063998613],"domain_scores_gemma":[0.9739106,0.004985575,0.0017844369,0.00052185234,0.017039327,0.0017581948],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0072616427,0.0011257527,0.0011231215,0.0052565574,0.0015521558,0.001366669,0.004032727,0.007818334,0.007835511],"category_scores_gemma":[0.029309474,0.0007032298,0.001059842,0.0037763747,0.0017635847,0.0009123933,0.0020413275,0.005125825,0.005499392],"study_design_candidate":"not_applicable","study_design_consensus":"not_applicable","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":true,"about_ca_system_consensus":false,"study_design_scores_codex":[0.000029277848,0.000045454963,0.0025270572,0.00025998286,0.000013725483,0.0005035066,0.00016115936,0.0001941861,0.00033792038,0.0013782186,0.93573135,0.05881813],"study_design_scores_gemma":[0.00011105306,0.000059637525,0.029160002,0.0040803053,0.00007865729,0.0046226173,0.00038128757,0.00055326824,0.0007714818,0.004090529,0.9560063,0.00008496069],"about_ca_topic_score_codex":0.244485,"about_ca_topic_score_gemma":0.35090756,"teacher_disagreement_score":0.99367815,"about_ca_system_score_codex":0.0063218456,"about_ca_system_score_gemma":0.026033953,"threshold_uncertainty_score":0.48612392},"labels":[],"label_agreement":null},{"id":"W2118787368","doi":"10.1111/cen.12766","title":"Metabolic profiling in Prader–Willi syndrome and nonsyndromic obesity: sex differences and the role of growth hormone","year":2015,"lang":"en","type":"article","venue":"Clinical Endocrinology","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":39,"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":"Eunice Kennedy Shriver National Institute of Child Health and Human Development; Canadian Institutes of Health Research; National Institutes of Health","keywords":"Ghrelin; Internal medicine; Endocrinology; Adiponectin; Leptin; Peptide YY; Medicine; Obesity; Insulin resistance; Insulin; Appetite; Hormone; Neuropeptide Y receptor; Neuropeptide","score_opus":0.025442535047017458,"score_gpt":0.2837858349495161,"score_spread":0.25834329990249866,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2118787368","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9978011,0.0011790558,0.0003868577,0.00005926598,0.000009523422,0.0000075447474,0.00013807681,0.000006308118,0.00041227095],"genre_scores_gemma":[0.99790084,0.0008290918,0.00068252295,0.000051814215,0.00001689531,0.000014863224,0.00015728928,0.0000060959123,0.00034059252],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9998204,0.000057080175,0.00002075408,0.00004476806,0.0000374919,0.000019469953],"domain_scores_gemma":[0.9997366,0.000059612616,0.00012827301,0.000016945403,0.00001760822,0.000040932526],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00032453457,0.00047707828,0.00029946186,0.0008371881,0.00015485592,0.0002501536,0.0001557566,0.00024129168,0.0012427965],"category_scores_gemma":[0.000909698,0.00016122527,0.0002690966,0.000526898,0.0002828899,0.00022142274,0.00035568353,0.00032034746,0.00012865172],"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":[0.0010527968,0.00005629715,0.95337874,0.00008917503,0.00013786681,0.002111089,0.00022225031,0.00008693103,0.0208643,0.00010981318,0.00012363418,0.02176701],"study_design_scores_gemma":[0.0000063745297,0.00015142541,0.9961598,0.000009916435,0.000019094423,0.0027472721,0.000068933885,0.00007372161,0.00054071203,0.000043227745,0.00017692639,0.0000026373598],"about_ca_topic_score_codex":0.0013465105,"about_ca_topic_score_gemma":0.0017771942,"teacher_disagreement_score":0.0013465105,"about_ca_system_score_codex":0.00014197543,"about_ca_system_score_gemma":0.00014829068,"threshold_uncertainty_score":0.004157543},"labels":[],"label_agreement":null},{"id":"W2120429387","doi":"10.1136/jmg.2005.037747","title":"Phenotype of triploid embryos: Table 1","year":2005,"lang":"en","type":"article","venue":"Journal of Medical Genetics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":160,"is_retracted":false,"has_abstract":true,"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":"Biology; Phenotype; Genomic imprinting; Embryo; Genetics; Ploidy; Placenta; Fetus; Imprinting (psychology); Embryogenesis; Population; Embryonic stem cell; Andrology; Gene; Pregnancy; Gene expression; DNA methylation","score_opus":0.011332655269697282,"score_gpt":0.26975413234574835,"score_spread":0.25842147707605106,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2120429387","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.93512124,0.0014461252,0.0064603584,0.00020842947,0.00005634091,0.0001315613,0.021648506,0.0005220867,0.034405317],"genre_scores_gemma":[0.9534882,0.0011654409,0.004475596,0.00014403845,0.000008447302,0.00013108172,0.014470849,0.00021880826,0.025897546],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9998735,0.0000151740605,0.000019347968,0.00003464514,0.00004206676,0.000015293566],"domain_scores_gemma":[0.99967515,0.00009233815,0.00008094248,0.00005117276,0.000041314295,0.00005912071],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00010638534,0.00029766202,0.00017265831,0.001059028,0.00023933084,0.00022815072,0.00020711249,0.00021492176,0.020119864],"category_scores_gemma":[0.00036940203,0.00007834587,0.00013822995,0.00034380538,0.00016755189,0.000132584,0.00026443895,0.00027681136,0.003606352],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0005363862,0.000057491503,0.019541726,0.00013911014,0.00003192063,0.004762594,0.00020756132,0.00016039416,0.9484156,0.00070406584,0.0019646797,0.023478515],"study_design_scores_gemma":[0.000067015506,0.0010616017,0.49485028,0.00014773948,0.00012890836,0.051736187,0.0005204741,0.0008586342,0.398801,0.0010308897,0.050722715,0.00007447847],"about_ca_topic_score_codex":0.0006871023,"about_ca_topic_score_gemma":0.0004522516,"teacher_disagreement_score":0.020119864,"about_ca_system_score_codex":0.00015318245,"about_ca_system_score_gemma":0.00010334495,"threshold_uncertainty_score":0.06730771},"labels":[],"label_agreement":null},{"id":"W2121126641","doi":"10.1210/jc.2009-0656","title":"Cardiovascular and Metabolic Risk Profile and Acylation-Stimulating Protein Levels in Children with Prader-Willi Syndrome and Effects of Growth Hormone Treatment","year":2010,"lang":"en","type":"article","venue":"The Journal of Clinical Endocrinology & Metabolism","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":34,"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":"Metabolic syndrome; Acylation; Endocrinology; Internal medicine; Hormone; Growth hormone; Growth hormone treatment; Medicine; Biology; Diabetes mellitus; Biochemistry","score_opus":0.011953373926264058,"score_gpt":0.27284551506717103,"score_spread":0.260892141140907,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2121126641","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9941414,0.005295623,0.00006486965,0.00009489953,0.000020724889,0.000042911037,0.000119963675,0.000004942255,0.00021456786],"genre_scores_gemma":[0.996079,0.0025116242,0.0005218346,0.00013523217,0.00008568961,0.00019973176,0.00035721916,0.0000026200944,0.000106958374],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9992156,0.00040241875,0.00007080702,0.00008226913,0.00014592674,0.00008305365],"domain_scores_gemma":[0.9984207,0.0007516092,0.00044042253,0.000044284785,0.000045738187,0.00029733885],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0010875283,0.00041362902,0.0010623346,0.00030015185,0.00024953665,0.00027333677,0.00023759698,0.00053524686,0.0007410453],"category_scores_gemma":[0.001996802,0.00017710666,0.00065809,0.00039775533,0.00048742877,0.00020504522,0.00018036873,0.0007033927,0.000058524085],"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":[0.18848962,0.0038183972,0.72337216,0.0015120509,0.0021465342,0.001575693,0.00019015613,0.001174455,0.010206659,0.0002068786,0.00087432587,0.06643303],"study_design_scores_gemma":[0.017324058,0.06178458,0.9132869,0.00015113862,0.001270475,0.002311396,0.00018753085,0.00053720496,0.0018186411,0.00009084552,0.0012144881,0.000022755195],"about_ca_topic_score_codex":0.0008631455,"about_ca_topic_score_gemma":0.0011060011,"teacher_disagreement_score":0.0010875283,"about_ca_system_score_codex":0.00029853598,"about_ca_system_score_gemma":0.00045813143,"threshold_uncertainty_score":0.0057514906},"labels":[],"label_agreement":null},{"id":"W2125827772","doi":"10.1002/ajmg.a.35651","title":"Mosaicism for genome‐wide paternal uniparental disomy with features of multiple imprinting disorders: Diagnostic and management issues","year":2012,"lang":"en","type":"article","venue":"American Journal of Medical Genetics Part A","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":89,"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":"","keywords":"Uniparental disomy; Genetics; Biology; Genomic imprinting; Angelman syndrome; Germline mosaicism; Copy-number variation; Genome; DNA methylation; Karyotype; Chromosome; Gene; Somatic cell","score_opus":0.006956413258992593,"score_gpt":0.25851707121315376,"score_spread":0.25156065795416116,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2125827772","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9398735,0.020389885,0.018288834,0.016163807,0.00022076043,0.00007175405,0.00013673851,0.00026536814,0.00458937],"genre_scores_gemma":[0.9874033,0.0033260088,0.007915446,0.00068386056,0.00034835067,0.000019551073,0.000043099928,0.000024068608,0.00023641116],"study_design_codex":"case_report","study_design_gemma":"case_report","domain_scores_codex":[0.99948454,0.00011751436,0.00007669688,0.0000894252,0.00012939247,0.000102406295],"domain_scores_gemma":[0.9985092,0.0007286712,0.00032096775,0.00007586627,0.0001316449,0.00023368522],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0012839333,0.00044461427,0.00048278435,0.0011766326,0.00040869814,0.00056955655,0.0009071282,0.0015575532,0.000619955],"category_scores_gemma":[0.0035909805,0.000305021,0.00019465662,0.00040980882,0.00090483634,0.00066259765,0.0005122162,0.0010485812,0.00024291675],"study_design_candidate":"case_report","study_design_consensus":"case_report","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00019039887,0.00008571684,0.37108672,0.00023575424,0.000037427417,0.4738251,0.00093086687,0.00080561126,0.024706941,0.0028189302,0.004089552,0.121187024],"study_design_scores_gemma":[0.000015856522,0.000119645265,0.043251127,0.00010732022,0.000029806664,0.94406337,0.0007672399,0.0030165813,0.0037448383,0.0016807555,0.0031810035,0.000022432065],"about_ca_topic_score_codex":0.0007194367,"about_ca_topic_score_gemma":0.0007760352,"teacher_disagreement_score":0.0015575532,"about_ca_system_score_codex":0.00033284153,"about_ca_system_score_gemma":0.0003851176,"threshold_uncertainty_score":0.006790161},"labels":[],"label_agreement":null},{"id":"W2126215378","doi":"10.1002/ajmg.a.20317","title":"X chromosome inactivation patterns in Russell–Silver syndrome patients and their mothers","year":2003,"lang":"en","type":"article","venue":"American Journal of Medical Genetics Part A","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":10,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Children’s Health Research Institute; BC Research (Canada); University of British Columbia","funders":"","keywords":"RSS; Uniparental disomy; Genetics; Biology; X chromosome; Allele; Skewed X-inactivation; Chromosome; X-inactivation; Karyotype; Gene","score_opus":0.006809157155739113,"score_gpt":0.23384114666269604,"score_spread":0.2270319895069569,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2126215378","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99947757,0.00012092328,0.000023611332,0.000017500193,0.0000024897697,0.0000023692023,0.0000679746,0.0000038610256,0.00028369436],"genre_scores_gemma":[0.99946517,0.00013014102,0.0000629543,0.000019414354,0.0000067841997,0.000006384907,0.00012223613,0.000004276057,0.00018268013],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99957436,0.0000843262,0.000048474645,0.0001184981,0.000109808025,0.00006447461],"domain_scores_gemma":[0.99917394,0.0002832603,0.00026097227,0.000048104834,0.000068715046,0.00016494845],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0003075832,0.00050729915,0.0005193155,0.0018347087,0.0004796226,0.00049938983,0.00034351085,0.0005582293,0.0021176534],"category_scores_gemma":[0.0023012047,0.00042274458,0.00021970918,0.00077478203,0.00048359638,0.00027173563,0.0004335695,0.00032568412,0.0005180849],"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":[0.0003929086,0.00007371218,0.97717446,0.000014899481,0.000030387722,0.010722523,0.0011637235,0.00004136397,0.0062577636,0.000051591378,0.00014737046,0.0039293035],"study_design_scores_gemma":[0.000026063539,0.00038838395,0.96600026,0.000015297494,0.00004098181,0.030795738,0.000921305,0.00015525798,0.0011309971,0.00006687382,0.00044141655,0.000017424862],"about_ca_topic_score_codex":0.0017122265,"about_ca_topic_score_gemma":0.00091388845,"teacher_disagreement_score":0.0021176534,"about_ca_system_score_codex":0.00031635637,"about_ca_system_score_gemma":0.00014005613,"threshold_uncertainty_score":0.00708431},"labels":[],"label_agreement":null},{"id":"W2126215690","doi":"10.1002/mc.20731","title":"Loss of imprinting and abnormal expression of the insulin‐like growth factor 2 gene in gastric cancer","year":2011,"lang":"en","type":"article","venue":"Molecular Carcinogenesis","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":22,"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; Imprinting (psychology); Genomic imprinting; Cancer; Insulin-like growth factor 2; Gene; Gene expression; Genetics; Cancer research; Growth factor; DNA methylation","score_opus":0.012808204426459757,"score_gpt":0.21367846563885082,"score_spread":0.20087026121239107,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2126215690","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9996654,0.00016175675,0.000041837895,0.000006898097,0.0000017167102,0.0000021042943,0.000021470722,0.0000014334885,0.000097501994],"genre_scores_gemma":[0.999814,0.0000661722,0.000025935458,0.0000065383583,0.0000041082567,0.0000012813508,0.000039389666,7.713777e-7,0.000041948242],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.999838,0.000029276136,0.000014800275,0.00004513323,0.000034253622,0.000038613627],"domain_scores_gemma":[0.99953985,0.00014707715,0.00012997276,0.00004003216,0.000040394913,0.00010271284],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00019912541,0.0001998705,0.0002773664,0.0007217657,0.00028032588,0.00026874407,0.00016874139,0.00022880905,0.0006451058],"category_scores_gemma":[0.00085914327,0.00021665847,0.00014468527,0.00041271193,0.0004701295,0.00019696592,0.00022580657,0.00021490965,0.000114470284],"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":[0.0002570707,0.000021776097,0.9882919,0.000015637017,0.00003202311,0.00058975193,0.00015708483,0.00003571656,0.008109991,0.000011585366,0.000026175589,0.0024513667],"study_design_scores_gemma":[0.0000069334387,0.0001475187,0.99678147,0.0000014679889,0.000019909403,0.0022171123,0.00008818806,0.00008508742,0.00052915263,0.000012323351,0.00010822497,0.000002544023],"about_ca_topic_score_codex":0.002099868,"about_ca_topic_score_gemma":0.0018087183,"teacher_disagreement_score":0.002099868,"about_ca_system_score_codex":0.00014908677,"about_ca_system_score_gemma":0.00012511935,"threshold_uncertainty_score":0.0041753054},"labels":[],"label_agreement":null},{"id":"W2126215730","doi":"10.1007/s00439-013-1379-z","title":"High frequency of copy number variations (CNVs) in the chromosome 11p15 region in patients with Beckwith–Wiedemann syndrome","year":2013,"lang":"en","type":"article","venue":"Human Genetics","topic":"Genetic Syndromes and Imprinting","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":"University of Calgary; SickKids Foundation; Centre Hospitalier Universitaire Sainte-Justine; University of Toronto; Hospital for Sick Children","funders":"","keywords":"Beckwith–Wiedemann syndrome; Biology; Genomic imprinting; Macroglossia; Copy-number variation; Genetics; Imprinting (psychology); Methylation; Uniparental disomy; Chromosome; Comparative genomic hybridization; DNA methylation; GiST; Gene duplication; Karyotype; Gene; Cancer research; Pathology; Medicine; Genome; Gene expression","score_opus":0.00915601971796006,"score_gpt":0.22020110568275408,"score_spread":0.21104508596479402,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2126215730","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99887496,0.00029208703,0.00023977189,0.00004417646,0.000008866769,0.0000034238176,0.000114111856,0.000012665498,0.0004099757],"genre_scores_gemma":[0.99958795,0.0000790923,0.00013601355,0.000013483821,0.0000085910515,0.0000025155214,0.00006390069,0.0000031186023,0.00010535884],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9996092,0.00007585502,0.00005583073,0.00011748554,0.0000918718,0.000049759983],"domain_scores_gemma":[0.99919707,0.0003673287,0.00023882915,0.00004052937,0.000051048533,0.000105158164],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00017372328,0.0004999323,0.0002882325,0.001881437,0.00039947234,0.00034476788,0.00029261387,0.0005814892,0.0027386085],"category_scores_gemma":[0.0017899565,0.0002329601,0.00020053402,0.0010891763,0.00038230684,0.00022841997,0.00031489125,0.00024822276,0.00018080072],"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":[0.0006812522,0.00006847431,0.9129227,0.000062009756,0.00016892693,0.025466746,0.0006385004,0.00042383862,0.042117666,0.00042145085,0.0005202544,0.0165083],"study_design_scores_gemma":[0.000033664724,0.00016411657,0.90840876,0.000021920789,0.00022342362,0.08286731,0.0004002296,0.0008588988,0.0054764515,0.00050057267,0.0010148977,0.000029742696],"about_ca_topic_score_codex":0.0011575861,"about_ca_topic_score_gemma":0.0011000937,"teacher_disagreement_score":0.0027386085,"about_ca_system_score_codex":0.00015082375,"about_ca_system_score_gemma":0.00018865708,"threshold_uncertainty_score":0.009161532},"labels":[],"label_agreement":null},{"id":"W2127028166","doi":"10.1152/physiolgenomics.00163.2003","title":"A survey of genetic and epigenetic variation affecting human gene expression","year":2004,"lang":"en","type":"article","venue":"Physiological Genomics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":262,"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 Health Centre; Université Laval; Université de Montréal; Centre Hospitalier Universitaire Sainte-Justine; McGill University; McGill University and Génome Québec Innovation Centre","funders":"","keywords":"Biology; Genetics; Allele; Gene; Single-nucleotide polymorphism; Epigenetics; Genetic variation; Linkage disequilibrium; Mendelian inheritance; Haplotype; Genotype","score_opus":0.02628550284291359,"score_gpt":0.2587019193799324,"score_spread":0.23241641653701883,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2127028166","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9786708,0.013184207,0.0042465664,0.00024737578,0.000010152964,0.000014896574,0.0017432511,0.000035387275,0.0018474227],"genre_scores_gemma":[0.9839061,0.008832798,0.0037244984,0.00019241632,0.0000467302,0.000022921997,0.002334403,0.000013083747,0.0009272389],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.999747,0.00005164658,0.000017458298,0.000098666715,0.00006521528,0.000020085332],"domain_scores_gemma":[0.99967337,0.00012292368,0.00008462451,0.00002630664,0.00004299852,0.000049819355],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00030665065,0.0001488673,0.00023422782,0.0010161051,0.00017274938,0.00023209213,0.000110914625,0.00021424024,0.0007724749],"category_scores_gemma":[0.0004827356,0.00006481971,0.00010449833,0.001317301,0.00022798721,0.00012110284,0.00014233206,0.00022748607,0.00018944427],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00044716697,0.00006585751,0.24927051,0.0004923756,0.00021531085,0.001458499,0.0004814277,0.00051767804,0.60894835,0.0008431425,0.00077484234,0.13648486],"study_design_scores_gemma":[0.000009127365,0.0004197765,0.93716466,0.00002714004,0.000095534044,0.0068940385,0.00020409867,0.00034668625,0.038813505,0.0006072056,0.015402379,0.000015954107],"about_ca_topic_score_codex":0.0005146028,"about_ca_topic_score_gemma":0.00061210373,"teacher_disagreement_score":0.0010161051,"about_ca_system_score_codex":0.00011226439,"about_ca_system_score_gemma":0.00014296253,"threshold_uncertainty_score":0.002584219},"labels":[],"label_agreement":null},{"id":"W2128052161","doi":"10.1016/j.jcjd.2014.07.170","title":"H19 Regulates Glucose-Induced Extracellular Matrix Protein Production in Diabetes","year":2014,"lang":"en","type":"article","venue":"Canadian Journal of Diabetes","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":1,"is_retracted":false,"has_abstract":false,"route_ca_aff":false,"route_ca_fund":false,"route_ca_venue":true,"route_about_ca":false,"ca_institutions":"","funders":"","keywords":"microRNA; Medicine; Gestational diabetes; Long non-coding RNA; Genomic imprinting; Non-coding RNA; Gene; MEG3; Coding (social sciences); RNA; Diabetes mellitus; Extracellular matrix; Computational biology; Bioinformatics; Genetics; Biology; Gene expression; Pregnancy; Endocrinology; DNA methylation; Gestation","score_opus":0.006948784916698735,"score_gpt":0.20384093814396922,"score_spread":0.1968921532272705,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2128052161","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9927038,0.0025592288,0.0009200667,0.00021674825,0.0000644468,0.00001570155,0.00062034157,0.00008237167,0.0028172992],"genre_scores_gemma":[0.99563956,0.00087197014,0.00048554162,0.000049705945,0.000016214026,0.000007386255,0.00038589412,0.000035438912,0.0025082931],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9998945,0.000011016541,0.0000053615886,0.000014687665,0.00003315995,0.000041306143],"domain_scores_gemma":[0.99983776,0.000027875492,0.000038723476,0.000010138056,0.000019428855,0.00006609197],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00009842135,0.00020960711,0.0001670123,0.0004885668,0.00032519546,0.0004367938,0.0004004278,0.00020996857,0.0021800532],"category_scores_gemma":[0.00015759758,0.00019506425,0.00018455759,0.00024701824,0.00029114512,0.00014964951,0.0002472786,0.00029157905,0.000320801],"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":[0.0010339703,0.00005110284,0.008009804,0.000020320984,0.000026974696,0.00072086044,0.000039203136,0.0001754063,0.983657,0.00050906715,0.00034948988,0.0054067625],"study_design_scores_gemma":[0.00014301606,0.00036769046,0.32471046,0.000015444997,0.000082651284,0.0011723329,0.00022491174,0.0015332347,0.6627224,0.0005898218,0.008408828,0.000029225357],"about_ca_topic_score_codex":0.0147462,"about_ca_topic_score_gemma":0.017324757,"teacher_disagreement_score":0.0147462,"about_ca_system_score_codex":0.0009639422,"about_ca_system_score_gemma":0.0004335606,"threshold_uncertainty_score":0.029320717},"labels":[],"label_agreement":null},{"id":"W2128106580","doi":"10.1152/ajpcell.00091.2008","title":"Functional characterization of NIPA2, a selective Mg<sup>2+</sup> transporter","year":2008,"lang":"en","type":"article","venue":"American Journal of Physiology-Cell Physiology","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":93,"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; University of British Columbia Hospital","funders":"Canadian Institutes of Health Research; University of British Columbia; Michael Smith Health Research BC","keywords":"Characterization (materials science); Transporter; Chemistry; Nanotechnology; Biochemistry; Materials science; Gene","score_opus":0.006838465224161937,"score_gpt":0.19976498484428376,"score_spread":0.19292651962012183,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2128106580","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.98757553,0.001522998,0.0067110085,0.00024061961,0.000037940415,0.000035202742,0.0024434824,0.000083008774,0.0013501226],"genre_scores_gemma":[0.98027694,0.000967658,0.009329523,0.00017066453,0.00003724733,0.00006585335,0.0056082373,0.00006083294,0.003483016],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9998816,0.000012197962,0.000009242775,0.000037376096,0.00004367367,0.00001592089],"domain_scores_gemma":[0.9998523,0.000033684064,0.000021291531,0.00001853379,0.000033839773,0.00004022859],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00012927089,0.00025402437,0.00034765704,0.00023962288,0.0002086319,0.00034422334,0.00022186252,0.00029500353,0.0009285061],"category_scores_gemma":[0.00023103942,0.00011658868,0.00023909661,0.00019789192,0.00019286491,0.00023031425,0.00015987869,0.00034386976,0.00055380043],"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":[0.00001950762,0.0000032477406,0.00026518333,0.000013991042,0.0000015128738,0.000045222598,0.0000056592407,0.000016224662,0.99922717,0.000028048007,0.000014977609,0.00035923728],"study_design_scores_gemma":[0.00001424548,0.00016250931,0.050536405,0.000006461299,0.00002760092,0.0020363007,0.00007850767,0.0033441419,0.93682766,0.00012969848,0.006824414,0.000012026963],"about_ca_topic_score_codex":0.0006615073,"about_ca_topic_score_gemma":0.0007933555,"teacher_disagreement_score":0.0009285061,"about_ca_system_score_codex":0.00025810482,"about_ca_system_score_gemma":0.00020748228,"threshold_uncertainty_score":0.0031061172},"labels":[],"label_agreement":null},{"id":"W2128356343","doi":"10.1158/0008-5472.can-11-2266","title":"Monoallelic Expression Determines Oncogenic Progression and Outcome in Benign and Malignant Brain Tumors","year":2011,"lang":"en","type":"article","venue":"Cancer Research","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":65,"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; Toronto General Hospital; Hospital for Sick Children","funders":"Canadian Institutes of Health Research; Hospital for Sick Children","keywords":"Carcinogenesis; Brain tumor; Tumor progression; Gene; IDH1; Cancer research; Biology; Cancer; Neuroblastoma; Medicine; Pathology; Genetics; Mutation","score_opus":0.09370436671842969,"score_gpt":0.39691019496942026,"score_spread":0.30320582825099057,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2128356343","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99788624,0.0007336793,0.0007429282,0.000022283415,0.0000022067923,0.0000050692347,0.00019397525,0.000015035797,0.0003985462],"genre_scores_gemma":[0.9991103,0.00020979517,0.00027530335,0.000010803847,0.0000040568207,0.000005382847,0.00021951461,0.000006071684,0.00015880846],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99974316,0.00004329863,0.000024221992,0.000085300366,0.000059262642,0.00004479672],"domain_scores_gemma":[0.99930036,0.000217532,0.0002668717,0.000063623054,0.00006391819,0.000087712855],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00026223858,0.00012306873,0.00022643416,0.00091191486,0.00017464555,0.00030797464,0.000119504984,0.0001949025,0.0006964361],"category_scores_gemma":[0.0008226101,0.00012584901,0.00012210425,0.00036875025,0.00021387919,0.0001503978,0.00023695901,0.00024656128,0.00019748852],"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":[0.00052111066,0.000036170488,0.585238,0.0000415071,0.00011406536,0.0004907783,0.00013693562,0.00014148642,0.4016675,0.00011357505,0.00007107277,0.011427763],"study_design_scores_gemma":[0.0000023647312,0.000071779825,0.9821326,0.000002635639,0.00003400658,0.0014145108,0.000053612945,0.00032138207,0.015485713,0.00016042164,0.00031614132,0.0000047247086],"about_ca_topic_score_codex":0.00041627162,"about_ca_topic_score_gemma":0.0006357139,"teacher_disagreement_score":0.00091191486,"about_ca_system_score_codex":0.000099540855,"about_ca_system_score_gemma":0.00008660034,"threshold_uncertainty_score":0.002329886},"labels":[],"label_agreement":null},{"id":"W2130225900","doi":"10.1136/jmg.40.4.249","title":"The imprinted region on human chromosome 7q32 extends to the carboxypeptidase A gene cluster: an imprinted candidate for Silver-Russell syndrome","year":2003,"lang":"en","type":"article","venue":"Journal of Medical Genetics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":50,"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","funders":"","keywords":"Genomic imprinting; Genetics; Biology; Imprinting (psychology); Epigenetics; Gene; Allele; Candidate gene; Gene cluster; Molecular biology; Gene expression; DNA methylation","score_opus":0.019663307049431717,"score_gpt":0.30436378464505703,"score_spread":0.28470047759562533,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2130225900","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9936906,0.0014960035,0.0033294302,0.00008188823,0.000013367109,0.000024175157,0.00040288086,0.00010055514,0.00086110074],"genre_scores_gemma":[0.9945997,0.00037472163,0.0034025894,0.000028494233,0.000020162548,0.00003330646,0.0006486992,0.000021981647,0.00087035244],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.99985373,0.000016834822,0.000007063806,0.00006521969,0.000040923853,0.000016291448],"domain_scores_gemma":[0.99985564,0.00005015468,0.00003542769,0.000014278496,0.000014756309,0.000029687028],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00009657921,0.000341539,0.00026210933,0.00070239196,0.00017009332,0.00013239689,0.00023718324,0.0002461338,0.0015939326],"category_scores_gemma":[0.00029556997,0.00019537735,0.00035128166,0.00024461336,0.00015355859,0.000084829,0.00023960505,0.00025079146,0.00044156975],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.000515848,0.00002880304,0.017652988,0.00007906764,0.00004209267,0.0018117883,0.00010516902,0.00028174685,0.96332353,0.00021073126,0.00014783423,0.015800325],"study_design_scores_gemma":[0.00011486579,0.0008576285,0.7011389,0.000055373734,0.00015849817,0.014565974,0.00009880798,0.003398229,0.2695045,0.00090716744,0.00916767,0.000032469074],"about_ca_topic_score_codex":0.0010435674,"about_ca_topic_score_gemma":0.0012234371,"teacher_disagreement_score":0.0015939326,"about_ca_system_score_codex":0.00015706861,"about_ca_system_score_gemma":0.00016513614,"threshold_uncertainty_score":0.005332291},"labels":[],"label_agreement":null},{"id":"W2130401515","doi":"10.1186/gb-2008-9-11-r160","title":"Characterization of the differentially methylated region of the Impact gene that exhibits Glires-specific imprinting","year":2008,"lang":"en","type":"article","venue":"Genome Biology","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":8,"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; University of Toronto","funders":"Ontario Ministry of Research and Innovation; Japan Society for the Promotion of Science; Hospital for Sick Children; Canadian Institutes of Health Research; Sick Kids Foundation; Genome Canada; Ontario Genomics; Ontario Genomics Institute; University of Toronto; GlaxoSmithKline","keywords":"Imprinting (psychology); Genomic imprinting; Genetics; Biology; Gene; Chemistry; Computational biology; DNA methylation; Gene expression","score_opus":0.023494236835081155,"score_gpt":0.2311479368331504,"score_spread":0.20765369999806926,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2130401515","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9946903,0.0004270965,0.0026910487,0.000019647505,0.00000663818,0.00002337718,0.001054866,0.000047741865,0.0010392827],"genre_scores_gemma":[0.99201876,0.0002491488,0.00386609,0.00004848,0.000009781222,0.000028800307,0.0028573023,0.000029877065,0.00089167315],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99994683,0.0000026642085,0.0000027136218,0.000020042922,0.000017130496,0.00001054129],"domain_scores_gemma":[0.99976474,0.000053431027,0.00008307965,0.000018911167,0.000022698574,0.000057262532],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.000071092516,0.00021146395,0.00020998118,0.0004582308,0.00012937274,0.00015285109,0.00020561436,0.0001891636,0.0014147151],"category_scores_gemma":[0.00021381475,0.000105313215,0.00023601673,0.00030861513,0.00023937262,0.00006682419,0.00016732694,0.0002688381,0.00042388777],"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":[0.00009328927,0.000008763745,0.0033468078,0.00003795614,0.000010316245,0.0001319744,0.000023566088,0.00004568562,0.9943757,0.000037372567,0.000013891228,0.0018746419],"study_design_scores_gemma":[0.00002744161,0.00040599823,0.41952968,0.000020699441,0.000121591715,0.0027948767,0.00010884806,0.0011949041,0.5717197,0.00016328425,0.0038966832,0.000016351822],"about_ca_topic_score_codex":0.00066844013,"about_ca_topic_score_gemma":0.001238247,"teacher_disagreement_score":0.0014147151,"about_ca_system_score_codex":0.00017055975,"about_ca_system_score_gemma":0.00017214262,"threshold_uncertainty_score":0.0047326684},"labels":[],"label_agreement":null},{"id":"W2130708302","doi":"10.1093/hmg/ddp465","title":"Dual effects of superovulation: loss of maternal and paternal imprinted methylation in a dose-dependent manner","year":2009,"lang":"en","type":"article","venue":"Human Molecular Genetics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":352,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Lawson Health Research Institute; Western University; Children’s Health Research Institute","funders":"Canadian Institutes of Health Research","keywords":"Genomic imprinting; Imprinting (psychology); Biology; DNA methylation; Blastocyst; Andrology; Oocyte; Methylation; Oogenesis; Embryo; Genetics; Endocrinology; Gene; Embryogenesis; Medicine","score_opus":0.006825363874313466,"score_gpt":0.24764202968685733,"score_spread":0.24081666581254388,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2130708302","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.98888737,0.0037277262,0.0043844334,0.0001665406,0.00006925292,0.00008500953,0.0006248142,0.00009550425,0.0019593006],"genre_scores_gemma":[0.99064916,0.0014226305,0.0023229243,0.0001869696,0.00002345387,0.0000930744,0.0006160564,0.00005161483,0.0046340255],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9996698,0.0000550811,0.000027432327,0.00008421692,0.00009771551,0.00006584026],"domain_scores_gemma":[0.9996933,0.000086382985,0.00007162461,0.000058476195,0.000024125618,0.00006623283],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00023832574,0.0003336539,0.00037284396,0.00036917356,0.00013067108,0.00026808024,0.00028742186,0.00034145077,0.002255274],"category_scores_gemma":[0.0002438663,0.00020358375,0.00041240107,0.00014374605,0.00033566664,0.00023546157,0.00051123695,0.0008698464,0.00026013362],"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":[0.00015451443,0.000022289294,0.00038032886,0.00003008821,0.000011386712,0.000049608065,0.000021291506,0.00003661761,0.99760807,0.000048329162,0.000022508717,0.0016150548],"study_design_scores_gemma":[0.000016994985,0.00090719265,0.010496551,0.0000070188134,0.000041539213,0.0002466224,0.00004056748,0.00051658414,0.9859146,0.00006670171,0.0017379719,0.000007693037],"about_ca_topic_score_codex":0.00084157754,"about_ca_topic_score_gemma":0.002019897,"teacher_disagreement_score":0.002255274,"about_ca_system_score_codex":0.00022308345,"about_ca_system_score_gemma":0.00029095393,"threshold_uncertainty_score":0.007544577},"labels":[],"label_agreement":null},{"id":"W2133615187","doi":"10.1093/humrep/den009","title":"Profound phenotypic variation among mice deficient in the maintenance of genomic imprints","year":2008,"lang":"en","type":"article","venue":"Human Reproduction","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":32,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Montreal Children's Hospital; McGill University","funders":"","keywords":"Genomic imprinting; Biology; Epigenetics; Phenotype; Embryo; Imprinting (psychology); Genetics; Somatic cell; Gestation; Fetus; Embryogenesis; Oocyte; Andrology; Gene; DNA methylation; Cell biology; Gene expression; Pregnancy","score_opus":0.018469781295581335,"score_gpt":0.23667707466583485,"score_spread":0.21820729337025352,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2133615187","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9944561,0.00066336873,0.002524755,0.000057960533,0.0000191938,0.000028659564,0.00093886757,0.00018520397,0.0011259032],"genre_scores_gemma":[0.9911766,0.0007179326,0.0031247833,0.000098538665,0.00001582436,0.000089769426,0.0017988584,0.00017331801,0.0028043936],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9996302,0.000032362677,0.00004508892,0.00013286511,0.00009081428,0.00006867703],"domain_scores_gemma":[0.99941826,0.000083032406,0.00022973455,0.00004516366,0.000029401868,0.00019441651],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0002874194,0.0006576775,0.00032981078,0.0011672188,0.00020164627,0.00038936082,0.00031864503,0.00052328117,0.0021281505],"category_scores_gemma":[0.00029818466,0.00038897464,0.00036451864,0.00025449126,0.00039009852,0.00021013439,0.00054624135,0.0010700282,0.00037957827],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.000115314644,0.0000248909,0.0010116078,0.000013629064,0.000013142978,0.00013390274,0.000016931794,0.000026046711,0.9977702,0.00006734504,0.000026255904,0.0007808635],"study_design_scores_gemma":[0.00010944561,0.0014140148,0.13642766,0.000046730336,0.00021920908,0.009639172,0.00009657841,0.00087451213,0.84817606,0.00032709716,0.002633979,0.000035534496],"about_ca_topic_score_codex":0.00022568191,"about_ca_topic_score_gemma":0.0003783159,"teacher_disagreement_score":0.0021281505,"about_ca_system_score_codex":0.00020971986,"about_ca_system_score_gemma":0.0001416917,"threshold_uncertainty_score":0.0071193576},"labels":[],"label_agreement":null},{"id":"W2133812508","doi":"10.1038/msb4100151","title":"Integrated proteomic and transcriptomic profiling of mouse lung development and Nmyc target genes","year":2007,"lang":"en","type":"article","venue":"Molecular Systems Biology","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":68,"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; Lunenfeld-Tanenbaum Research Institute; Mount Sinai Hospital; University of Toronto","funders":"Natural Sciences and Engineering Research Council of Canada; Canadian Institutes of Health Research; Ontario Genomics; Ontario Genomics Institute; Genome Canada","keywords":"Biology; Transcriptome; Gene; Gene expression profiling; Gene expression; Microarray analysis techniques; Microarray; Messenger RNA; DNA microarray; Molecular biology; Genetics; Cell biology","score_opus":0.007581777617385549,"score_gpt":0.22736491781211265,"score_spread":0.2197831401947271,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2133812508","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.98945236,0.0012392274,0.0063392036,0.000031278687,0.0000048197476,0.000013993056,0.002268483,0.000086333486,0.0005643232],"genre_scores_gemma":[0.9780804,0.0010901606,0.013551943,0.00007428406,0.000008776401,0.000060338447,0.004687743,0.00004294359,0.0024033976],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9998975,0.000008359041,0.0000061001224,0.00003318441,0.000038520368,0.000016348578],"domain_scores_gemma":[0.9999107,0.000013600059,0.000029431454,0.000007774841,0.000014565847,0.000023868733],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00010606485,0.00022369559,0.00019264621,0.00046115744,0.000101131474,0.00018783574,0.00012424207,0.00013290512,0.00037685534],"category_scores_gemma":[0.00008266324,0.000112279595,0.0001602919,0.00027859295,0.00011427222,0.000108985216,0.00012256234,0.00021152949,0.00013798277],"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":[0.00004776918,0.0000029250448,0.00060372136,0.00001212624,0.0000033907563,0.000017432252,0.0000031995205,0.00004304167,0.9984907,0.000017188164,0.0000087123235,0.000749877],"study_design_scores_gemma":[0.000007410977,0.00012882463,0.0769518,0.0000064350234,0.000035581408,0.00040232344,0.000030091924,0.0021350333,0.9188648,0.000090154084,0.0013398145,0.000007660794],"about_ca_topic_score_codex":0.0004917221,"about_ca_topic_score_gemma":0.0010198681,"teacher_disagreement_score":0.0004917221,"about_ca_system_score_codex":0.00017291663,"about_ca_system_score_gemma":0.00011104384,"threshold_uncertainty_score":0.0012606978},"labels":[],"label_agreement":null},{"id":"W2134155328","doi":"10.1093/bfgp/elq017","title":"Applications of the site-specific recombinase Cre to the study of genomic imprinting","year":2010,"lang":"en","type":"review","venue":"Briefings in Functional Genomics","topic":"Genetic Syndromes and Imprinting","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":"Canadian Institutes of Health Research; Michael Smith Health Research BC","keywords":"Biology; Recombinase; Genomic imprinting; Cre-Lox recombination; Cre recombinase; Imprinting (psychology); Genetics; Gene; Computational biology; Genome; Recombination; Transgene; Gene expression; DNA methylation","score_opus":0.024776814631630457,"score_gpt":0.26202048754038704,"score_spread":0.2372436729087566,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2134155328","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":[0.00017918719,0.9952957,0.000916848,0.00035556479,0.0005478126,0.000010179576,0.000026195336,0.000019459407,0.0026489906],"genre_scores_gemma":[0.00052137364,0.9972728,0.0006386536,0.00019735155,0.00025074897,0.000008614125,0.000042760606,0.0000028664244,0.0010649065],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.99976486,0.00003487377,0.000028775212,0.00005686576,0.00009330454,0.00002140798],"domain_scores_gemma":[0.9996356,0.0001700784,0.000041696643,0.000019289684,0.00008004805,0.00005321265],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0007418024,0.0011818003,0.0012944093,0.0026169964,0.0002583323,0.00078739354,0.0011355852,0.0012082694,0.003596361],"category_scores_gemma":[0.00058375904,0.0004551916,0.00043261788,0.0022628757,0.00085522037,0.001311433,0.0007241529,0.0022915343,0.004125959],"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":[0.00007479942,0.000081455924,0.00017309184,0.010750066,0.00007174228,0.0006141885,0.000060558825,0.0005115744,0.01358357,0.00711107,0.031237204,0.93573076],"study_design_scores_gemma":[0.000013494406,0.00005346912,0.00053878775,0.00079842407,0.000040649706,0.001860759,0.00003065575,0.000055542016,0.0024753741,0.001939058,0.9921731,0.000020726427],"about_ca_topic_score_codex":0.00090674247,"about_ca_topic_score_gemma":0.001448503,"teacher_disagreement_score":0.003596361,"about_ca_system_score_codex":0.0008635433,"about_ca_system_score_gemma":0.00090351613,"threshold_uncertainty_score":0.012031019},"labels":[],"label_agreement":null},{"id":"W2135010797","doi":"10.1530/eje-08-0462","title":"Long-acting octreotide treatment causes a sustained decrease in ghrelin concentrations but does not affect weight, behaviour and appetite in subjects with Prader–Willi syndrome","year":2008,"lang":"en","type":"article","venue":"European Journal of Endocrinology","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":79,"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; BC Children's Hospital; University of British Columbia","funders":"National Institute for Health and Care Research; Yale University","keywords":"Ghrelin; Appetite; Internal medicine; Endocrinology; Affect (linguistics); Octreotide; Medicine; Obesity; Psychology; Hormone; Somatostatin","score_opus":0.014235827869000966,"score_gpt":0.23881687054280548,"score_spread":0.22458104267380452,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2135010797","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9993476,0.00037610796,0.00007107741,0.000015666272,0.000014356382,0.000066996334,0.000021434971,0.000004963676,0.00008165223],"genre_scores_gemma":[0.9983279,0.0005700932,0.00038291278,0.000082977815,0.000049427872,0.00013556698,0.00011740693,0.000003089242,0.00033055866],"study_design_codex":"randomized_trial","study_design_gemma":"nonrandomized_trial","domain_scores_codex":[0.9996718,0.00014477006,0.00004411353,0.000047056248,0.000050689214,0.000041619132],"domain_scores_gemma":[0.9995016,0.000138561,0.0001390045,0.000031480056,0.000028266642,0.00016111339],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0008070517,0.00060162606,0.0011319715,0.00017814743,0.00024554945,0.0002393473,0.00029250066,0.00054208754,0.0013841221],"category_scores_gemma":[0.00066096726,0.00035873218,0.0004728907,0.00016629657,0.0006045993,0.00032218208,0.00019181901,0.00081276696,0.00017575765],"study_design_candidate":"nonrandomized_trial","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.650826,0.0417522,0.05285339,0.00084599503,0.0015677762,0.0007798281,0.0002351837,0.000725487,0.17501721,0.0000909532,0.0004071376,0.074898906],"study_design_scores_gemma":[0.109278284,0.75658613,0.12204436,0.000048115573,0.00065841334,0.0007444798,0.00014533025,0.00063845987,0.009034443,0.000037766127,0.0007624833,0.000021723486],"about_ca_topic_score_codex":0.0007089735,"about_ca_topic_score_gemma":0.0014523116,"teacher_disagreement_score":0.0013841221,"about_ca_system_score_codex":0.00021290722,"about_ca_system_score_gemma":0.000360349,"threshold_uncertainty_score":0.004630327},"labels":[],"label_agreement":null},{"id":"W2135284044","doi":"10.1002/(sici)1521-1878(200005)22:5<452::aid-bies7>3.0.co;2-k","title":"Mechanisms leading to uniparental disomy and their clinical consequences","year":2000,"lang":"en","type":"review","venue":"BioEssays","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":334,"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 Research (Canada)","funders":"","keywords":"Uniparental disomy; Biology; Genetics; Imprinting (psychology); Genomic imprinting; Somatic cell; Gamete; Mitotic crossover; Chromosome; Phenotype; Karyotype; Mutation; Gene","score_opus":0.06745023611415106,"score_gpt":0.3633006515805042,"score_spread":0.2958504154663531,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2135284044","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":[0.00047671012,0.99686986,0.00032863507,0.000168839,0.00013860836,0.0000044227113,0.00001704378,0.000019421199,0.001976571],"genre_scores_gemma":[0.0019108924,0.9962913,0.0002735194,0.00015681781,0.00010856147,0.0000062698064,0.00003700137,0.0000018724495,0.0012137425],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.9998354,0.00002380776,0.000026159132,0.000032605654,0.0000632235,0.000018953488],"domain_scores_gemma":[0.9998665,0.00004975338,0.000032140724,0.000006239255,0.000029160994,0.000016139686],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0003259199,0.0009419004,0.0010186436,0.0020343813,0.00022343533,0.0006488922,0.0007338326,0.00083580957,0.0027916168],"category_scores_gemma":[0.00040328293,0.00021059332,0.00030217346,0.0018222003,0.00055721635,0.0007964631,0.00039051208,0.00069975253,0.0029300512],"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":[0.00010802543,0.000056300956,0.00084085576,0.008586508,0.00009799276,0.002399762,0.000099962854,0.0003887356,0.0070813843,0.003742326,0.018034736,0.9585633],"study_design_scores_gemma":[0.000032618427,0.00012518442,0.0035504147,0.0017947631,0.00013055286,0.01933913,0.00014464025,0.00011116742,0.0036924635,0.004406563,0.966644,0.000028596727],"about_ca_topic_score_codex":0.00055091927,"about_ca_topic_score_gemma":0.000923397,"teacher_disagreement_score":0.0027916168,"about_ca_system_score_codex":0.0005709175,"about_ca_system_score_gemma":0.0004892635,"threshold_uncertainty_score":0.009338856},"labels":[],"label_agreement":null},{"id":"W2135374196","doi":"10.1002/ajmg.a.31404","title":"Cornelia de Lange syndrome: Parental preferences regarding the provision of medical information","year":2006,"lang":"en","type":"article","venue":"American Journal of Medical Genetics Part A","topic":"Genetic Syndromes and Imprinting","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":"Hospital for Sick Children","funders":"Cornelia de Lange Syndrome Foundation","keywords":"Cornelia de Lange Syndrome; Medicine; Preference; Medical information; Health care; Health information; Information needs; Family medicine; Psychiatry; Pediatrics","score_opus":0.008614901002602688,"score_gpt":0.2598341247911243,"score_spread":0.2512192237885216,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2135374196","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9991985,0.0002210253,0.00006689582,0.00011733708,0.000004318692,0.000004102084,0.00002392365,0.0000017064939,0.00036234563],"genre_scores_gemma":[0.9995291,0.000204857,0.000106444466,0.000042222975,0.0000035697315,0.0000035863834,0.000020821513,9.0334356e-7,0.00008858934],"study_design_codex":"observational","study_design_gemma":"qualitative","domain_scores_codex":[0.99851495,0.00082322024,0.00013794242,0.000059452108,0.0002924558,0.00017193148],"domain_scores_gemma":[0.9902007,0.005787737,0.0025786546,0.00020582692,0.0005897327,0.00063739164],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0023859877,0.0002243954,0.00023792866,0.0005828867,0.00063059136,0.0008101499,0.00014622492,0.000280524,0.001626319],"category_scores_gemma":[0.015577526,0.00018335051,0.00023748353,0.00053083524,0.0005016028,0.0005979035,0.0005573478,0.00043108768,0.0001387889],"study_design_candidate":"qualitative","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00018701683,0.000078927194,0.9627079,0.000060284598,0.00002676238,0.0015472955,0.017450633,0.000091605616,0.00065324013,0.00010950162,0.00042004432,0.016666792],"study_design_scores_gemma":[0.000042501568,0.00090613693,0.8580758,0.00018883453,0.000093911,0.008465657,0.12675805,0.000832679,0.0010658366,0.00028318347,0.0032276495,0.00005972422],"about_ca_topic_score_codex":0.005916485,"about_ca_topic_score_gemma":0.006597827,"teacher_disagreement_score":0.005916485,"about_ca_system_score_codex":0.00051669293,"about_ca_system_score_gemma":0.00047379083,"threshold_uncertainty_score":0.012618482},"labels":[],"label_agreement":null},{"id":"W2135386003","doi":"10.1186/1755-8166-4-15","title":"Context-based FISH localization of genomic rearrangements within chromosome 15q11.2q13 duplicons","year":2011,"lang":"en","type":"article","venue":"Molecular Cytogenetics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":10,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Genome Canada; Western University","funders":"Schulich School of Medicine and Dentistry; Natural Sciences and Engineering Research Council of Canada; London Health Sciences Centre","keywords":"Biology; Genetics; Pseudogene; Breakpoint; Chromosome; Context (archaeology); Fluorescence in situ hybridization; Gene dosage; Comparative genomic hybridization; Copy-number variation; Haploinsufficiency; Chromosomal rearrangement; Gene; Genome; Karyotype; Molecular biology; Phenotype; Gene expression","score_opus":0.02220257242134981,"score_gpt":0.22848057034702163,"score_spread":0.2062779979256718,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2135386003","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.98659295,0.00057054235,0.010606219,0.000055883545,0.000008274808,0.000025638426,0.00020954022,0.00011134669,0.0018197116],"genre_scores_gemma":[0.98975986,0.00027675126,0.008794215,0.0000191408,0.0000032839678,0.000024283712,0.00022086744,0.000016045427,0.0008854997],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99990356,0.00001128238,0.000005952511,0.000045867273,0.000016516611,0.000016702032],"domain_scores_gemma":[0.9999167,0.0000254745,0.000025554333,0.000010438414,0.000008379938,0.00001352623],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00014112148,0.00023707405,0.00012251618,0.0003790115,0.00018019871,0.00017601273,0.0001880836,0.00019365102,0.0020373536],"category_scores_gemma":[0.000253118,0.00017290625,0.000109730914,0.00019868107,0.0003299611,0.00014887085,0.00024969608,0.00022170346,0.0002857606],"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":[0.00004139585,0.0000029526823,0.001250403,0.000023704853,0.000004566788,0.00008700729,0.00002520665,0.000097277145,0.9973648,0.00013384018,0.000014836977,0.000954087],"study_design_scores_gemma":[0.000024806524,0.00028519437,0.05581868,0.000013870998,0.000058682584,0.0022993719,0.00011969317,0.001841348,0.9361244,0.00027989916,0.0031249153,0.000009195701],"about_ca_topic_score_codex":0.0011920269,"about_ca_topic_score_gemma":0.0030890238,"teacher_disagreement_score":0.0020373536,"about_ca_system_score_codex":0.00034638433,"about_ca_system_score_gemma":0.0001489674,"threshold_uncertainty_score":0.0068156123},"labels":[],"label_agreement":null},{"id":"W2135611636","doi":"10.1210/jc.2007-2633","title":"Selective Loss of MEG3 Expression and Intergenic Differentially Methylated Region Hypermethylation in the MEG3/DLK1 Locus in Human Clinically Nonfunctioning Pituitary Adenomas","year":2008,"lang":"en","type":"article","venue":"The Journal of Clinical Endocrinology & Metabolism","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":142,"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":"Jarislowsky Foundation; National Institute of Diabetes and Digestive and Kidney Diseases; Massachusetts General Hospital; National Institutes of Health; Pfizer","keywords":"MEG3; Biology; DNA methylation; Pituitary neoplasm; Pituitary tumors; Pituitary adenoma; Methylation; Adenoma; Pituitary gland; Endocrinology; Gene expression; Gene; Long non-coding RNA; RNA; Genetics; Hormone","score_opus":0.03647789990591279,"score_gpt":0.32855109320403725,"score_spread":0.2920731932981245,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2135611636","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99926263,0.00019781095,0.0002496152,0.000009068411,0.0000016420042,0.000004453625,0.00010707586,0.000008772055,0.00015895737],"genre_scores_gemma":[0.99944884,0.00006845594,0.00016414818,0.0000072040016,0.0000016187771,0.0000048905727,0.00018430929,0.000003395506,0.00011701063],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9998969,0.000011165397,0.000011070924,0.00003196014,0.000030529987,0.0000184163],"domain_scores_gemma":[0.9998406,0.000043627588,0.000046907855,0.000019140392,0.000018859144,0.000030775976],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00011662182,0.00019516564,0.0001745345,0.0004577968,0.00017967884,0.0001600593,0.00014253892,0.00017192068,0.00078752934],"category_scores_gemma":[0.0002457373,0.0001312027,0.00013941349,0.00024933854,0.00029400704,0.00006919273,0.00016579784,0.00015834213,0.00016701994],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00041896984,0.000010437949,0.026952688,0.000034748464,0.000016387718,0.0008139125,0.00010181943,0.000045973295,0.9701634,0.0000186967,0.000026781127,0.0013961586],"study_design_scores_gemma":[0.000042870284,0.00051600346,0.6060863,0.0000051165425,0.00008555292,0.010714317,0.0003050863,0.00054585485,0.38051656,0.00008774384,0.0010824999,0.00001209062],"about_ca_topic_score_codex":0.0016516738,"about_ca_topic_score_gemma":0.0020787437,"teacher_disagreement_score":0.0016516738,"about_ca_system_score_codex":0.00026268524,"about_ca_system_score_gemma":0.00015428803,"threshold_uncertainty_score":0.003284037},"labels":[],"label_agreement":null},{"id":"W2135835560","doi":"10.1074/jbc.m112.372094","title":"Mutations in the GlyT2 Gene (SLC6A5) Are a Second Major Cause of Startle Disease","year":2012,"lang":"en","type":"article","venue":"Journal of Biological Chemistry","topic":"Genetic Syndromes and Imprinting","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":"Children's Hospital of Eastern Ontario","funders":"Action Medical Research","keywords":"Gene; Disease; Genetics; Mutation; Medicine; Biology; Internal medicine","score_opus":0.023963068138088232,"score_gpt":0.26389123899218403,"score_spread":0.2399281708540958,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2135835560","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9957561,0.0014477356,0.0014302146,0.000060529535,0.0000168779,0.000016858177,0.0004747211,0.00008079565,0.0007161495],"genre_scores_gemma":[0.99775827,0.00047512978,0.00073633454,0.000034591572,0.000013472316,0.0000074167415,0.0004104064,0.000007754576,0.00055663555],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.99984884,0.00002051336,0.000018456856,0.00004586931,0.000045582292,0.000020789119],"domain_scores_gemma":[0.9998355,0.00003009681,0.00005989862,0.0000063795046,0.0000133463,0.000054653534],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00014023346,0.00096449524,0.00031801502,0.00052149536,0.00023097731,0.00027306273,0.00014618087,0.00041615692,0.0019660634],"category_scores_gemma":[0.00038219715,0.00009755182,0.00032054752,0.00029499427,0.0002633784,0.00010492429,0.0002960731,0.00016753208,0.0003374942],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0012935189,0.00008100397,0.21407537,0.0005109923,0.00051703,0.10185298,0.00076312025,0.00081673585,0.64396393,0.0006366566,0.0012544411,0.034234144],"study_design_scores_gemma":[0.00011907605,0.0006154079,0.66007996,0.00009558071,0.0003480981,0.23814188,0.00031740658,0.0017732766,0.08789915,0.0004490679,0.010114474,0.00004659738],"about_ca_topic_score_codex":0.0006760928,"about_ca_topic_score_gemma":0.00068817113,"teacher_disagreement_score":0.0019660634,"about_ca_system_score_codex":0.00022816379,"about_ca_system_score_gemma":0.00013200157,"threshold_uncertainty_score":0.006577134},"labels":[],"label_agreement":null},{"id":"W2136629665","doi":"10.1093/hmg/ddn344","title":"Necdin, a Prader-Willi syndrome candidate gene, regulates gonadotropin-releasing hormone neurons during development","year":2008,"lang":"en","type":"article","venue":"Human Molecular Genetics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":103,"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":"National Institute of Environmental Health Sciences; National Institute of General Medical Sciences; Eunice Kennedy Shriver National Institute of Child Health and Human Development; National Institute of Diabetes and Digestive and Kidney Diseases; National Cancer Institute","keywords":"Biology; Gonadotropin-releasing hormone; Endocrinology; Internal medicine; Homeobox; Psychological repression; Repressor; Gene; Enhancer; Transcription factor; Gene expression; Cell biology; Hormone; Genetics; Luteinizing hormone; Medicine","score_opus":0.012659921166068804,"score_gpt":0.2227246949130071,"score_spread":0.21006477374693827,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2136629665","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9960418,0.0006759751,0.0018588881,0.00005921782,0.000014484574,0.000011828371,0.0002250642,0.00008507319,0.0010277173],"genre_scores_gemma":[0.9927856,0.00073761964,0.0021985853,0.000046891255,0.000004896499,0.000025204838,0.0004529476,0.000024965655,0.0037234176],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9999553,0.000006588051,0.0000045571774,0.000016280597,0.000010919533,0.0000063595844],"domain_scores_gemma":[0.9999279,0.000010425677,0.000026736734,0.0000055055475,0.000007954958,0.000021526064],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00003796184,0.00027643502,0.0001042199,0.00017519445,0.000097623386,0.00012495338,0.00013009792,0.00017789689,0.0007857128],"category_scores_gemma":[0.00014446043,0.000117467716,0.00010961651,0.00006000117,0.00014899354,0.00009264464,0.00022569204,0.00024235711,0.00025705984],"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":[0.0000688766,0.0000059867884,0.0019426502,0.00002023922,0.0000042634006,0.00094080827,0.000023560156,0.000059995604,0.9944753,0.00007752237,0.00006389082,0.002316971],"study_design_scores_gemma":[0.00004745942,0.00032463524,0.23943794,0.000028934219,0.000053372936,0.015224835,0.00013702722,0.0026256153,0.7320327,0.00024174395,0.009825843,0.000019843174],"about_ca_topic_score_codex":0.00045643814,"about_ca_topic_score_gemma":0.00092851534,"teacher_disagreement_score":0.0007857128,"about_ca_system_score_codex":0.00017541827,"about_ca_system_score_gemma":0.00012986726,"threshold_uncertainty_score":0.0026284456},"labels":[],"label_agreement":null},{"id":"W2136943416","doi":"10.1136/jmg.40.11.e126","title":"Identification of eight novel <i>NSD1</i> mutations in Sotos syndrome","year":2003,"lang":"en","type":"article","venue":"Journal of Medical Genetics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":35,"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 Health; University of Calgary","funders":"Core Research for Evolutional Science and Technology; Japan Science and Technology Corporation; Università degli Studi di Siena; Friedrich-Schiller-Universität Jena","keywords":"Sotos syndrome; Haploinsufficiency; Frontal Bossing; Gigantism; Genetics; Exon; Pituitary disorder; Point mutation; Biology; Craniofacial; Mutation; Medicine; Gene; Endocrinology; Anatomy; Phenotype","score_opus":0.012018203080545279,"score_gpt":0.27070369433063374,"score_spread":0.25868549125008844,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2136943416","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99764013,0.00035737833,0.00054075336,0.00008371171,0.000044926343,0.00003948198,0.00031542196,0.00003791358,0.0009402134],"genre_scores_gemma":[0.9979128,0.00019082594,0.0010693041,0.00009033626,0.00003234401,0.000020601263,0.0004546963,0.0000130392045,0.00021603006],"study_design_codex":"case_report","study_design_gemma":"observational","domain_scores_codex":[0.99975103,0.00001620055,0.000044828266,0.000063796746,0.000080843776,0.000043333348],"domain_scores_gemma":[0.9996425,0.00008867419,0.00008203987,0.000016305752,0.00002879255,0.0001417204],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00014797428,0.0010396611,0.0004784942,0.000874047,0.00035709454,0.00048517826,0.0006608533,0.0011835059,0.0015264425],"category_scores_gemma":[0.00073593925,0.00026174323,0.0005507593,0.00048805575,0.0006192957,0.00018651436,0.0005015958,0.00040262105,0.00038931484],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0012940334,0.0003418543,0.20205282,0.0003379394,0.0001963956,0.42004013,0.0019369969,0.0015167386,0.3394515,0.0012297527,0.002377476,0.029224457],"study_design_scores_gemma":[0.0004267799,0.00097563065,0.4267821,0.00014881557,0.0004356041,0.46351013,0.0008013866,0.0053477613,0.076812625,0.00091784575,0.023643319,0.00019801084],"about_ca_topic_score_codex":0.0012035227,"about_ca_topic_score_gemma":0.001290343,"teacher_disagreement_score":0.0015264425,"about_ca_system_score_codex":0.00040228077,"about_ca_system_score_gemma":0.00026225156,"threshold_uncertainty_score":0.005106449},"labels":[],"label_agreement":null},{"id":"W2137283728","doi":"10.1128/mcb.21.7.2384-2392.2001","title":"Establishment and Maintenance of DNA Methylation Patterns in Mouse <i>Ndn</i> : Implications for Maintenance of Imprinting in Target Genes of the Imprinting Center","year":2001,"lang":"en","type":"article","venue":"Molecular and Cellular Biology","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":50,"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":"Division of Materials Research","keywords":"Genomic imprinting; Biology; Imprinting (psychology); DNA methylation; Epigenetics; Genetics; Blastocyst; Methylation; Gene; CpG site; Bisulfite sequencing; DNA demethylation; Oocyte; RNA-Directed DNA Methylation; Molecular biology; Embryo; Embryogenesis; Gene expression","score_opus":0.007802827356174907,"score_gpt":0.22995713498546852,"score_spread":0.2221543076292936,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2137283728","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99187183,0.001280619,0.004417921,0.00007282242,0.000010968902,0.000017823551,0.000548178,0.000074767726,0.0017049892],"genre_scores_gemma":[0.992765,0.0007029298,0.002265336,0.000058484544,0.000004773745,0.000038950115,0.0008502536,0.0000367657,0.0032775272],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99988425,0.00000864527,0.000010363723,0.00004384062,0.00003023216,0.00002260558],"domain_scores_gemma":[0.9998404,0.000014657709,0.00005209376,0.00002931616,0.0000242295,0.000039394763],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00016093897,0.00015482934,0.00012146599,0.00027676043,0.00016784821,0.00026061395,0.00034266515,0.00023326524,0.0006164599],"category_scores_gemma":[0.00018136812,0.00018533651,0.00019738385,0.000083834,0.0002659378,0.0002897335,0.00025398924,0.00033818072,0.00023333868],"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":[0.00005071432,0.0000048115394,0.0023809571,0.000014777187,0.0000045122492,0.00003185286,0.000038052018,0.000029270583,0.9955592,0.00020577767,0.000014831712,0.0016652113],"study_design_scores_gemma":[0.000016850307,0.00017489519,0.1200951,0.00001406256,0.00003246539,0.00050988863,0.00008599851,0.0005316666,0.8746417,0.00028308187,0.0036032617,0.000011130025],"about_ca_topic_score_codex":0.0020039903,"about_ca_topic_score_gemma":0.0030586743,"teacher_disagreement_score":0.0020039903,"about_ca_system_score_codex":0.00039471555,"about_ca_system_score_gemma":0.00021864133,"threshold_uncertainty_score":0.00398463},"labels":[],"label_agreement":null},{"id":"W2137790269","doi":"10.1002/ca.22659","title":"Angelman syndrome: A review highlighting musculoskeletal and anatomical aberrations","year":2015,"lang":"en","type":"review","venue":"Clinical Anatomy","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","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":"Medicine; Angelman syndrome; Physical medicine and rehabilitation; Genetics","score_opus":0.058183020319579344,"score_gpt":0.4222337289677908,"score_spread":0.3640507086482115,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2137790269","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":[0.0008232462,0.99790096,0.00012226688,0.00027971825,0.0001773611,0.000004069228,0.000043254477,0.000013329333,0.0006358973],"genre_scores_gemma":[0.004905632,0.9937465,0.00033518826,0.00025127796,0.00039269577,0.0000059071867,0.000094413,0.000003525916,0.0002648113],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.99964786,0.000051141702,0.00012816867,0.0000690769,0.000078180754,0.000025475374],"domain_scores_gemma":[0.9991903,0.00039735506,0.00022367875,0.000018311952,0.00010973882,0.0000606303],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00040738765,0.0010891177,0.0012994386,0.0076636765,0.0003622974,0.0008988784,0.0009776806,0.0009094107,0.0024551912],"category_scores_gemma":[0.0012770079,0.00029318075,0.0006086169,0.0056131734,0.0005559805,0.0015504705,0.0005854557,0.000955396,0.00080513745],"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":[0.0001654851,0.000093254275,0.006217993,0.059768435,0.0003848717,0.023689143,0.00074352627,0.00076126336,0.004326916,0.002765365,0.058638446,0.84244543],"study_design_scores_gemma":[0.000027235668,0.00018397399,0.014257738,0.021119528,0.00074632926,0.16975786,0.00065014965,0.00021874512,0.00082542765,0.0019510287,0.79018104,0.00008097932],"about_ca_topic_score_codex":0.0016675855,"about_ca_topic_score_gemma":0.0025656363,"teacher_disagreement_score":0.0076636765,"about_ca_system_score_codex":0.0005477598,"about_ca_system_score_gemma":0.0012112366,"threshold_uncertainty_score":0.00821346},"labels":[],"label_agreement":null},{"id":"W2138958826","doi":"10.1093/toxsci/kfs303","title":"Identification of Dlk1-Dio3 Imprinted Gene Cluster Noncoding RNAs as Novel Candidate Biomarkers for Liver Tumor Promotion","year":2012,"lang":"en","type":"article","venue":"Toxicological Sciences","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":69,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Discovery Centre","funders":"Cancer Research UK","keywords":"MEG3; Biology; Epigenetics; Gene expression; microRNA; Cancer research; Gene; Carcinogenesis; Genetics; RNA; Long non-coding RNA","score_opus":0.03815984994435082,"score_gpt":0.30712325360777937,"score_spread":0.2689634036634285,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2138958826","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99094266,0.0021861529,0.0054079844,0.00007317525,0.000009691266,0.000025888246,0.0005280984,0.00007790721,0.0007483704],"genre_scores_gemma":[0.99517125,0.0007315854,0.0026675728,0.00004152702,0.0000043715218,0.000018918729,0.00045016233,0.0000097414995,0.000904899],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99993,0.000010340206,0.000004118934,0.00002493622,0.000018543806,0.000011966993],"domain_scores_gemma":[0.9997806,0.000043523905,0.00010152739,0.000015727786,0.000020450785,0.000038149567],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00013288585,0.000221709,0.00013641434,0.00030932412,0.00008261651,0.00016282736,0.000086615044,0.00014033592,0.0006600671],"category_scores_gemma":[0.00018454615,0.00008113033,0.000088222965,0.00014746453,0.00020371153,0.00014021929,0.00013279796,0.00022720231,0.00013649123],"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":[0.00020147684,0.000008046953,0.0065054796,0.000028257338,0.0000046323116,0.000055279987,0.000012466099,0.000041215786,0.99070704,0.000060848473,0.000012679812,0.0023625568],"study_design_scores_gemma":[0.000009479187,0.00027544185,0.101723105,0.0000050662034,0.00003465643,0.0003993013,0.00003792329,0.0006258308,0.8955261,0.000116027666,0.0012415942,0.0000054841394],"about_ca_topic_score_codex":0.0003699961,"about_ca_topic_score_gemma":0.00085835904,"teacher_disagreement_score":0.0006600671,"about_ca_system_score_codex":0.0002188405,"about_ca_system_score_gemma":0.0001631581,"threshold_uncertainty_score":0.0022081137},"labels":[],"label_agreement":null},{"id":"W2139222393","doi":"10.1071/rd05118","title":"Gamete imprinting: setting epigenetic patterns for the next generation","year":2005,"lang":"en","type":"review","venue":"Reproduction Fertility and Development","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":126,"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; Montreal Children's Hospital","funders":"Canadian Institutes of Health Research; McGill University; National Institutes of Health; Brandeis University","keywords":"Epigenetics; Genomic imprinting; DNA methylation; Biology; Gamete; Imprinting (psychology); Offspring; Germline; Genetics; Epigenesis; Carcinogenesis; Function (biology); Gene; Gene expression; Pregnancy","score_opus":0.11650807665525371,"score_gpt":0.32474064821823473,"score_spread":0.20823257156298103,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2139222393","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":[0.00023548934,0.99445057,0.0011983372,0.00047543665,0.00037782622,0.000007236026,0.000023238816,0.000030909636,0.0032009922],"genre_scores_gemma":[0.0010879408,0.9955858,0.0007850078,0.000219938,0.00017243813,0.000009572358,0.000036944606,0.0000035688224,0.0020987373],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.9998586,0.000029021605,0.000014749529,0.000024507024,0.000060450635,0.000012641378],"domain_scores_gemma":[0.99981064,0.000076651544,0.000029732213,0.000009761353,0.00004510011,0.000028267024],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0005383408,0.0008676002,0.0013571868,0.0015025926,0.00029541555,0.0010696107,0.0010669002,0.0012631941,0.0032503172],"category_scores_gemma":[0.00048135666,0.00019875192,0.00021075943,0.00167611,0.00076222996,0.0014493391,0.00066654,0.0010916657,0.0041397572],"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":[0.000038988484,0.000031320717,0.0002538153,0.0057038125,0.000048217957,0.0003800236,0.00009341993,0.0003652221,0.0036753747,0.006804571,0.021970244,0.960635],"study_design_scores_gemma":[0.000006900316,0.000042223226,0.00070053845,0.0009157432,0.000032623193,0.0020375452,0.00011340501,0.00006947273,0.0011100029,0.0031412086,0.99181515,0.000015104569],"about_ca_topic_score_codex":0.0008456051,"about_ca_topic_score_gemma":0.0016351715,"teacher_disagreement_score":0.0032503172,"about_ca_system_score_codex":0.0007304759,"about_ca_system_score_gemma":0.00084960746,"threshold_uncertainty_score":0.010873437},"labels":[],"label_agreement":null},{"id":"W2140288082","doi":"10.1242/dev.045724","title":"Activation of paternally expressed genes and perinatal death caused by deletion of the<i>Gtl2</i>gene","year":2010,"lang":"en","type":"article","venue":"Development","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":138,"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 Institutes of Health; Division of Materials Research; Jarislowsky Foundation; National Institute of Diabetes and Digestive and Kidney Diseases; Massachusetts General Hospital","keywords":"Biology; Genomic imprinting; Gene; Locus (genetics); Genetics; Exon; Imprinting (psychology); Gene expression; MEG3; DNA methylation; Regulation of gene expression; Molecular biology; Long non-coding RNA; RNA","score_opus":0.007019756044616067,"score_gpt":0.2072545216897211,"score_spread":0.20023476564510503,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2140288082","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9935347,0.0010651262,0.0029878323,0.000097271164,0.000026797805,0.00001348594,0.00057144667,0.00012858334,0.0015747375],"genre_scores_gemma":[0.9938069,0.00062116294,0.0011014325,0.00008271351,0.000007955668,0.0000324009,0.0005927758,0.00005772957,0.003696904],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9998161,0.000025487196,0.000022506898,0.00005129593,0.000043310058,0.000041339],"domain_scores_gemma":[0.9998086,0.00003042362,0.00007149303,0.000021092063,0.000008420697,0.000059929065],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00012788302,0.00046027012,0.00021910692,0.00022967572,0.000105700354,0.00026998654,0.00031951143,0.0003211609,0.0013194167],"category_scores_gemma":[0.00011607231,0.00025135736,0.00022758779,0.00011515256,0.00027223246,0.000126951,0.0003497864,0.0006715911,0.0005211279],"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":[0.00017093835,0.000012976595,0.00067257264,0.000025467514,0.000007766145,0.00044158415,0.000017309745,0.000050629606,0.9976568,0.00012209806,0.000028006627,0.0007939094],"study_design_scores_gemma":[0.000028640654,0.00020278367,0.00946506,0.0000092395385,0.00003183629,0.0018150536,0.00003479929,0.0004636027,0.9862844,0.000050302693,0.001608408,0.0000058293995],"about_ca_topic_score_codex":0.00055688823,"about_ca_topic_score_gemma":0.0007661975,"teacher_disagreement_score":0.0013194167,"about_ca_system_score_codex":0.0002475697,"about_ca_system_score_gemma":0.00021375586,"threshold_uncertainty_score":0.004413843},"labels":[],"label_agreement":null},{"id":"W2140384819","doi":"10.1111/j.1469-185x.2008.00050.x","title":"Genomic imprinting in the development and evolution of psychotic spectrum conditions","year":2008,"lang":"en","type":"review","venue":"Biological reviews/Biological reviews of the Cambridge Philosophical Society","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":93,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Simon Fraser University","funders":"","keywords":"Genomic imprinting; Angelman syndrome; Rett syndrome; Autism; Epigenetics; Imprinting (psychology); Genetics; Psychology; Autism spectrum disorder; Neurodevelopmental disorder; Pervasive developmental disorder; Biology; Neuroscience; Gene; DNA methylation; Developmental psychology; Gene expression","score_opus":0.10805341932226731,"score_gpt":0.3308161649552741,"score_spread":0.2227627456330068,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2140384819","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":[0.0024354106,0.9887256,0.00072468957,0.0035880795,0.0017434641,0.000010526467,0.000049040584,0.000021962069,0.0027012688],"genre_scores_gemma":[0.010861297,0.98266935,0.0005105428,0.0014305752,0.0031438456,0.000015256287,0.000050109287,0.000008835642,0.0013102018],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.99986696,0.000033561366,0.0000221582,0.000024428358,0.000027377882,0.000025499532],"domain_scores_gemma":[0.9994659,0.0003339629,0.00011802342,0.000009402673,0.000031290576,0.000041373296],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0004959792,0.0006020129,0.00054841547,0.001446562,0.00025906262,0.00090536586,0.0006122721,0.0011253705,0.0020919123],"category_scores_gemma":[0.0012892858,0.00017032346,0.0003231628,0.0012712016,0.00091886095,0.00091034785,0.0008321722,0.0011091025,0.00087737007],"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":[0.00023984944,0.000070684466,0.007054655,0.010602281,0.00032668366,0.0028586874,0.0010716879,0.0023277632,0.004843288,0.03613381,0.08126505,0.8532057],"study_design_scores_gemma":[0.000013689073,0.00023767955,0.015266636,0.0040518,0.00023480476,0.0060763466,0.00065687316,0.0002539414,0.0010287275,0.014137163,0.9580045,0.000037844642],"about_ca_topic_score_codex":0.0011123472,"about_ca_topic_score_gemma":0.0016014864,"teacher_disagreement_score":0.0020919123,"about_ca_system_score_codex":0.0007977795,"about_ca_system_score_gemma":0.00053434155,"threshold_uncertainty_score":0.0069981217},"labels":[],"label_agreement":null},{"id":"W2142247682","doi":"10.1111/j.1420-9101.2006.01091.x","title":"Imbalanced genomic imprinting in brain development: an evolutionary basis for the aetiology of autism","year":2006,"lang":"en","type":"review","venue":"Journal of Evolutionary Biology","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":148,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Simon Fraser University","funders":"","keywords":"Autism; Genomic imprinting; Angelman syndrome; Rett syndrome; Biology; Imprinting (psychology); Neurodevelopmental disorder; Epigenetics; Brain size; Cognition; Neuroscience; Developmental disorder; Brain development; Genetics; Gene; Psychology; Developmental psychology; DNA methylation","score_opus":0.023966328968371902,"score_gpt":0.3058627408149343,"score_spread":0.2818964118465624,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2142247682","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":[0.00020026675,0.99778074,0.00028572924,0.00043665673,0.00021398008,0.0000025340821,0.000008766399,0.000010283137,0.001061048],"genre_scores_gemma":[0.0012347414,0.9974589,0.000312453,0.00015965177,0.00021816544,0.000003896462,0.000013567539,0.0000011421434,0.0005975245],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.9998789,0.000019342942,0.000014015516,0.000029269348,0.000044931894,0.000013514179],"domain_scores_gemma":[0.9997714,0.00010230253,0.000028039076,0.000008296329,0.000054702334,0.000035330748],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0005671932,0.0008432002,0.0012408161,0.001708366,0.00028743118,0.0008431576,0.0011806762,0.0016299208,0.0029255368],"category_scores_gemma":[0.00062357076,0.00020334357,0.00023828394,0.0017137342,0.00095427973,0.0015854079,0.0006550883,0.001209894,0.0024864848],"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":[0.00008748353,0.000039088398,0.00043508495,0.0048525576,0.00004837879,0.000682927,0.00007014853,0.00045779295,0.002186785,0.006118619,0.018967755,0.9660533],"study_design_scores_gemma":[0.000033293087,0.000098722456,0.0025717204,0.00215064,0.00008652956,0.0064545725,0.00017242396,0.00016273478,0.00091006,0.010283021,0.97704554,0.00003083068],"about_ca_topic_score_codex":0.0009851035,"about_ca_topic_score_gemma":0.0013174276,"teacher_disagreement_score":0.0029255368,"about_ca_system_score_codex":0.0006924473,"about_ca_system_score_gemma":0.0007620832,"threshold_uncertainty_score":0.009786904},"labels":[],"label_agreement":null},{"id":"W2142314133","doi":"10.1210/jc.2010-1733","title":"The Metabolic Phenotype of Prader-Willi Syndrome (PWS) in Childhood: Heightened Insulin Sensitivity Relative to Body Mass Index","year":2010,"lang":"en","type":"article","venue":"The Journal of Clinical Endocrinology & Metabolism","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":106,"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; University of Alberta","keywords":"Internal medicine; Endocrinology; Adiponectin; Insulin resistance; Medicine; Resistin; Context (archaeology); Insulin; Leptin; Body mass index; Quantitative insulin sensitivity check index; Metabolic syndrome; Obesity; Biology; Insulin sensitivity","score_opus":0.014008731554147806,"score_gpt":0.30542488526259487,"score_spread":0.2914161537084471,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2142314133","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9995622,0.00012766755,0.00008324522,0.00001854165,0.0000036910242,0.0000042719676,0.00006145462,0.0000038210173,0.00013516027],"genre_scores_gemma":[0.99941957,0.0001573614,0.00023291065,0.000013439701,0.0000103093535,0.0000067867827,0.00011848765,0.0000016201058,0.00003952989],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9997255,0.000075094074,0.000031811844,0.00008088066,0.000046011293,0.000040632443],"domain_scores_gemma":[0.9993912,0.000112615686,0.0003296926,0.00003348878,0.000034406166,0.00009860997],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0002464614,0.0006818238,0.00036058677,0.0007728232,0.00031616763,0.00032067043,0.00020762836,0.00031137874,0.0011639018],"category_scores_gemma":[0.0012217951,0.00022791962,0.0002102376,0.0006049388,0.00056873227,0.00030948047,0.0005240803,0.00039080647,0.00014081768],"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":[0.00023499671,0.00003421359,0.99185175,0.000029137447,0.000044251443,0.0020799104,0.00009130526,0.000064742344,0.0025385597,0.000040900613,0.000070462105,0.0029197172],"study_design_scores_gemma":[0.000009577509,0.00019533899,0.989661,0.000009851873,0.00002260896,0.009400979,0.00014424107,0.00010019876,0.00030861713,0.000034343546,0.00010913837,0.0000040719674],"about_ca_topic_score_codex":0.0011673665,"about_ca_topic_score_gemma":0.001457614,"teacher_disagreement_score":0.0011673665,"about_ca_system_score_codex":0.00017115,"about_ca_system_score_gemma":0.00020846288,"threshold_uncertainty_score":0.0038936138},"labels":[],"label_agreement":null},{"id":"W2143629379","doi":"10.1093/hmg/ddr018","title":"Disruption of genomic neighbourhood at the imprinted IGF2-H19 locus in Beckwith–Wiedemann syndrome and Silver–Russell syndrome","year":2011,"lang":"en","type":"article","venue":"Human Molecular Genetics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":93,"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","funders":"Hutchison Whampoa Limited; Ministero dell’Istruzione, dell’Università e della Ricerca; University of Cambridge; Cancer Research UK","keywords":"CTCF; Cohesin; Genomic imprinting; Biology; Beckwith–Wiedemann syndrome; Chromatin; Genetics; Epigenetics; Locus (genetics); Histone; Imprinting (psychology); DNA methylation; MEG3; Heterochromatin; Molecular biology; Enhancer; Gene; Gene expression","score_opus":0.013939239669072904,"score_gpt":0.23091790155132244,"score_spread":0.21697866188224954,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2143629379","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9990614,0.00012164808,0.00038804644,0.000013140824,0.0000039815377,0.0000041409735,0.00007844399,0.000012043355,0.00031718472],"genre_scores_gemma":[0.99902916,0.0000904946,0.0004407485,0.000015003229,0.0000028866618,0.00000686022,0.00016638634,0.000007172451,0.00024124508],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9998338,0.000030405563,0.000027601223,0.00004227115,0.000037307862,0.000028466571],"domain_scores_gemma":[0.9998915,0.0000237987,0.00003204231,0.000008357078,0.000004537628,0.000039723043],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.000079516045,0.00039356056,0.00017901824,0.00058835663,0.00015105474,0.00015274182,0.00013051654,0.0002753156,0.0014074778],"category_scores_gemma":[0.00030333555,0.00023067754,0.00028518657,0.0002487174,0.00026745987,0.00006123384,0.00025497677,0.00024719117,0.00019423092],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00056206045,0.000046590492,0.044261787,0.00004228763,0.00009408783,0.010669981,0.00022889097,0.0002211816,0.9390668,0.00035503248,0.00009957008,0.004351737],"study_design_scores_gemma":[0.00015483635,0.0007120612,0.67734545,0.000025413996,0.00022976924,0.10521826,0.00045232684,0.0017961751,0.2107778,0.00042973095,0.0028144775,0.00004366573],"about_ca_topic_score_codex":0.0015898205,"about_ca_topic_score_gemma":0.0028936602,"teacher_disagreement_score":0.0015898205,"about_ca_system_score_codex":0.00014442847,"about_ca_system_score_gemma":0.00013717572,"threshold_uncertainty_score":0.004708469},"labels":[],"label_agreement":null},{"id":"W2143659807","doi":"10.1186/1741-7007-8-105","title":"The Drosophila homolog of the mammalian imprint regulator, CTCF, maintains the maternal genomic imprint in Drosophila melanogaster","year":2010,"lang":"en","type":"article","venue":"BMC Biology","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":17,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Mount Allison University; Dalhousie University","funders":"Dalhousie University; Wayne State University","keywords":"CTCF; Biology; Genomic imprinting; Chromatin; Genetics; Insulator (electricity); Drosophila melanogaster; X-inactivation; Epigenetics; Regulator; DNA methylation; Heterochromatin; Gene; Imprinting (psychology); X chromosome; Gene expression; Enhancer","score_opus":0.007678675970868722,"score_gpt":0.22997203241391445,"score_spread":0.22229335644304574,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2143659807","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.44720715,0.1746167,0.079783686,0.036457434,0.020232506,0.0004860355,0.023894073,0.014014254,0.20330824],"genre_scores_gemma":[0.78904027,0.028938662,0.01239642,0.0053275805,0.0016272705,0.00015811992,0.008730147,0.0009098523,0.15287176],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99983954,0.000012172302,0.000007881855,0.000037668407,0.000078490935,0.00002413207],"domain_scores_gemma":[0.9998517,0.000026156265,0.00003371107,0.000016171954,0.00003413646,0.00003811715],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00018377214,0.00040700936,0.00031502848,0.00026003493,0.00034121305,0.00048221956,0.00069437956,0.0010654096,0.0063944403],"category_scores_gemma":[0.00039567624,0.00023442913,0.00020529698,0.0001943128,0.0002492943,0.00031354828,0.0003457168,0.00083170965,0.0043558837],"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":[0.00020931503,0.000015503265,0.00080082886,0.00061136734,0.000017101424,0.0004622097,0.00005230885,0.00019452229,0.9242423,0.0021565738,0.028363531,0.042874467],"study_design_scores_gemma":[0.00012747034,0.0002569129,0.018097607,0.0001402317,0.00007808032,0.0010629318,0.00010274786,0.0014415156,0.5656598,0.0008031511,0.41219485,0.00003478095],"about_ca_topic_score_codex":0.0022009057,"about_ca_topic_score_gemma":0.005382949,"teacher_disagreement_score":0.0063944403,"about_ca_system_score_codex":0.0007883639,"about_ca_system_score_gemma":0.000376572,"threshold_uncertainty_score":0.02139157},"labels":[],"label_agreement":null},{"id":"W2144824933","doi":"10.1101/gr.192278.115","title":"The landscape of genomic imprinting across diverse adult human tissues","year":2015,"lang":"en","type":"article","venue":"Genome Research","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":239,"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":"Common Fund; National Institute of Biomedical Imaging and Bioengineering; National Institute of Neurological Disorders and Stroke; National Institute of General Medical Sciences; National Cancer Institute; National Human Genome Research Institute; University of Miami; Natural Sciences and Engineering Research Council of Canada; National Institutes of Health; Orionin Tutkimussäätiö; Université de Genève; National Institute of Mental Health; National Heart, Lung, and Blood Institute; Emil Aaltosen Säätiö; Israel Science Foundation; U.S. Public Health Service; Suomen Kulttuurirahasto; Roswell Park Cancer Institute; Hewlett-Packard Development Company; German-Israeli Foundation for Scientific Research and Development; Broad Institute; University of North Carolina; NIH Office of the Director; Van Andel Research Institute; National Institute on Drug Abuse; Science Applications International Corporation; University of Oxford; University of Chicago; Harvard University","keywords":"Imprinting (psychology); Genomic imprinting; Biology; Genetics; Gene; Allele; Gene expression; Gene expression profiling; DNA methylation","score_opus":0.06576906099941318,"score_gpt":0.37813869640297826,"score_spread":0.3123696354035651,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2144824933","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99387616,0.002586186,0.0016032859,0.00003558811,0.00000211306,0.0000046267837,0.0007644091,0.000030245292,0.001097364],"genre_scores_gemma":[0.9975374,0.00084160664,0.0006829677,0.00003201739,0.0000058165933,0.0000071970017,0.0005012224,0.000015714122,0.00037609987],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.99984777,0.000029003802,0.000010523281,0.00006036455,0.000030867028,0.00002147804],"domain_scores_gemma":[0.99973446,0.00010256104,0.00007898561,0.00003631248,0.000023693923,0.000023938266],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0001454756,0.00010982053,0.00022610107,0.0006685577,0.0001230266,0.00035172218,0.00011051682,0.000104215615,0.00095351995],"category_scores_gemma":[0.00039473214,0.00012649641,0.00009167381,0.0006064305,0.00021949773,0.0001247573,0.00023940776,0.00013219996,0.00018251847],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00049762253,0.000015298163,0.18890502,0.00013002336,0.0002071045,0.0006989451,0.00043654352,0.00050958706,0.754724,0.00042865804,0.00020267615,0.0532445],"study_design_scores_gemma":[0.000005938782,0.000104517385,0.96353376,0.000009197376,0.00006438515,0.0017263455,0.000116620926,0.00034005218,0.031639986,0.00053210696,0.0019185405,0.000008551487],"about_ca_topic_score_codex":0.0006805307,"about_ca_topic_score_gemma":0.0009788106,"teacher_disagreement_score":0.00095351995,"about_ca_system_score_codex":0.000112463036,"about_ca_system_score_gemma":0.00008194597,"threshold_uncertainty_score":0.0031898618},"labels":[],"label_agreement":null},{"id":"W2145160468","doi":"10.1093/humupd/dmh002","title":"Potential significance of genomic imprinting defects for reproduction and assisted reproductive technology","year":2004,"lang":"en","type":"review","venue":"Human Reproduction Update","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":196,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Montreal Children's Hospital","funders":"","keywords":"Genomic imprinting; Reprogramming; Biology; Imprinting (psychology); Epigenetics; Germ cell; Genetics; Assisted reproductive technology; Epigenesis; DNA methylation; Infertility; Gene; Pregnancy; Gene expression","score_opus":0.023741709619292253,"score_gpt":0.29728737863305993,"score_spread":0.2735456690137677,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2145160468","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":[0.00032707644,0.99633765,0.00030964584,0.0004791169,0.00022491472,0.000003264314,0.0000133222175,0.000012859052,0.0022922189],"genre_scores_gemma":[0.0021743448,0.99558747,0.00039140502,0.00025814827,0.00021561199,0.0000062191334,0.000026976635,0.0000020283169,0.0013378048],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.9998267,0.000039180515,0.000021185764,0.000026057418,0.000072131515,0.000014712814],"domain_scores_gemma":[0.99966097,0.00019369063,0.000044618828,0.00001317429,0.000058377518,0.000029236637],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00044164006,0.0005580205,0.000854607,0.0012779813,0.00021223677,0.00066565786,0.0006255195,0.0010923163,0.0039921114],"category_scores_gemma":[0.00082016306,0.00013505341,0.00022248231,0.0015230065,0.0005598422,0.0009146721,0.00035863539,0.0007344553,0.0020435445],"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":[0.00006115967,0.000032305164,0.000612232,0.004798471,0.00006297533,0.0018557368,0.00007880216,0.0002937636,0.003643318,0.0080833975,0.020017011,0.9604607],"study_design_scores_gemma":[0.00002102668,0.00008774388,0.002746431,0.0013674066,0.00008524216,0.011392974,0.00012343426,0.000080940896,0.0014904564,0.004910667,0.97767365,0.000019989848],"about_ca_topic_score_codex":0.0010554739,"about_ca_topic_score_gemma":0.0015333103,"teacher_disagreement_score":0.0039921114,"about_ca_system_score_codex":0.0006100063,"about_ca_system_score_gemma":0.0009117454,"threshold_uncertainty_score":0.013354957},"labels":[],"label_agreement":null},{"id":"W2145188829","doi":"10.1242/dev.096511","title":"The imprinted polycomb group gene <i>Sfmbt2</i> is required for trophoblast maintenance and placenta development","year":2013,"lang":"en","type":"article","venue":"Development","topic":"Genetic Syndromes and Imprinting","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","funders":"Eunice Kennedy Shriver National Institute of Child Health and Human Development; National Institute of General Medical Sciences","keywords":"Trophoblast; Biology; Genomic imprinting; Placenta; Inner cell mass; Embryonic stem cell; Embryo; Embryogenesis; Gene; Genetics; Imprinting (psychology); Parthenogenesis; Allele; Cell biology; Stem cell; Blastocyst; Gene expression; DNA methylation; Fetus; Pregnancy","score_opus":0.008274921547472978,"score_gpt":0.20902618053516658,"score_spread":0.2007512589876936,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2145188829","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9893076,0.0017824337,0.0056857485,0.00011804335,0.000024380772,0.000011372656,0.000859233,0.0001898513,0.0020213353],"genre_scores_gemma":[0.9954432,0.00045304536,0.0013371722,0.000022480188,0.000006739742,0.000009320137,0.000734968,0.000028336295,0.0019646483],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9998814,0.000013942815,0.000012543753,0.000026136422,0.000043603657,0.00002239653],"domain_scores_gemma":[0.9998398,0.000020941912,0.000058088823,0.000018126168,0.000009579004,0.00005348388],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00007215966,0.00029613802,0.00018805922,0.00030670795,0.00018590146,0.0002706218,0.00017063199,0.0001989988,0.0013114904],"category_scores_gemma":[0.00018248489,0.00013770767,0.00017564255,0.00019031749,0.00029936762,0.0001383939,0.0002467059,0.00030397245,0.00033435476],"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":[0.000043004406,0.000002855855,0.0009280362,0.000019132836,0.000004928883,0.00020407347,0.000013771274,0.000031104446,0.99712104,0.00012817408,0.000043756634,0.0014602079],"study_design_scores_gemma":[0.000016296428,0.000065445776,0.054177463,0.0000076183037,0.00002272777,0.0025082666,0.000030806765,0.000834732,0.9368688,0.00012242819,0.0053385673,0.000006810617],"about_ca_topic_score_codex":0.001593353,"about_ca_topic_score_gemma":0.0022877164,"teacher_disagreement_score":0.001593353,"about_ca_system_score_codex":0.00023652744,"about_ca_system_score_gemma":0.00022504204,"threshold_uncertainty_score":0.004387319},"labels":[],"label_agreement":null},{"id":"W2145709837","doi":"10.1086/497540","title":"Children with Idiopathic Hemihypertrophy and Beckwith-Wiedemann Syndrome Have Different Constitutional Epigenotypes Associated with Wilms Tumor","year":2005,"lang":"en","type":"article","venue":"The American Journal of Human Genetics","topic":"Genetic Syndromes and Imprinting","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":"University of Alberta","funders":"National Cancer Institute; Robert Wood Johnson Foundation; Foundation for the National Institutes of Health","keywords":"Hemihypertrophy; Wilms' tumor; Beckwith–Wiedemann syndrome; Epigenetics; Medicine; Imprinting (psychology); Genomic imprinting; Internal medicine; Pathology; DNA methylation; Biology; Genetics; Gene","score_opus":0.006669921147059524,"score_gpt":0.21626906855544475,"score_spread":0.20959914740838523,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2145709837","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9985759,0.00008454346,0.00021067998,0.000021767062,0.000005107592,0.0000035904816,0.00016404956,0.000012970255,0.0009213082],"genre_scores_gemma":[0.9988223,0.00014002115,0.00046055464,0.000017400595,0.000014831165,0.000009609732,0.00023974554,0.000016731054,0.0002788719],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99960846,0.000085131556,0.000042159736,0.00008094241,0.00006962105,0.00011376975],"domain_scores_gemma":[0.99910945,0.00042667397,0.00024933595,0.000053334123,0.000028891318,0.00013227416],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00021031438,0.0006417472,0.00038725123,0.0015674722,0.0003727363,0.0003636967,0.00030070407,0.0004609841,0.003987427],"category_scores_gemma":[0.0014601948,0.00034603465,0.00023269327,0.00095281604,0.0007383307,0.00037723905,0.0006243629,0.0002769901,0.00028666572],"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":[0.00260459,0.00013816821,0.7800284,0.000102533064,0.00017134366,0.040409315,0.00158366,0.0005610478,0.15547356,0.0034287237,0.00045250432,0.015046207],"study_design_scores_gemma":[0.00009844422,0.00026514722,0.91383296,0.000016229707,0.00013454638,0.072488986,0.00072277506,0.0003787587,0.010182696,0.0007393558,0.0011091945,0.000030828283],"about_ca_topic_score_codex":0.0005480074,"about_ca_topic_score_gemma":0.0009936601,"teacher_disagreement_score":0.003987427,"about_ca_system_score_codex":0.00014197355,"about_ca_system_score_gemma":0.00017591323,"threshold_uncertainty_score":0.013339281},"labels":[],"label_agreement":null},{"id":"W2145851060","doi":"10.1101/gr.2609605","title":"Structural and functional analysis of a 0.5-Mb chicken region orthologous to the imprinted mammalian <i>Ascl2/Mash2–Igf2–H19</i> region","year":2004,"lang":"en","type":"article","venue":"Genome Research","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":47,"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; RIKEN; Ministry of Education, Culture, Sports, Science and Technology","keywords":"Biology; Genomic imprinting; Imprinting (psychology); Genetics; Gene; Exon; Intron; Evolutionary biology; Gene expression","score_opus":0.04462871531326501,"score_gpt":0.3041135668515461,"score_spread":0.2594848515382811,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2145851060","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99730694,0.0003750106,0.0012910528,0.00001655006,0.0000066063926,0.000011830593,0.00048789944,0.000017194445,0.00048684853],"genre_scores_gemma":[0.9924119,0.00016869101,0.0037641253,0.00003183995,0.000007307406,0.000014444483,0.0025309527,0.000018767769,0.0010518788],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.99995255,0.0000044569974,0.0000033223018,0.000021802873,0.000010038291,0.000007814631],"domain_scores_gemma":[0.9998846,0.000025282628,0.000029207837,0.0000108705635,0.000014295738,0.000035695793],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.000055146884,0.00020342814,0.00012142523,0.00019535013,0.00016555678,0.00013098645,0.000173663,0.00017941486,0.0007192495],"category_scores_gemma":[0.00012824497,0.00014378333,0.00021083561,0.00011842967,0.0001495398,0.00006771624,0.00012158176,0.00018489119,0.00036295096],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00010429906,0.0000061093647,0.0008201457,0.000020526151,0.000003550887,0.000072790266,0.00001920756,0.000036748563,0.99807173,0.000025880932,0.000011584099,0.000807402],"study_design_scores_gemma":[0.000053863776,0.0005801216,0.46024334,0.000024360872,0.00009871377,0.0015285173,0.0001640275,0.0030997645,0.5266513,0.00007368642,0.007467003,0.000015201933],"about_ca_topic_score_codex":0.003492452,"about_ca_topic_score_gemma":0.003930162,"teacher_disagreement_score":0.003492452,"about_ca_system_score_codex":0.00021011417,"about_ca_system_score_gemma":0.0001381542,"threshold_uncertainty_score":0.006944239},"labels":[],"label_agreement":null},{"id":"W2146264881","doi":"10.1146/annurev.cellbio.24.110707.175418","title":"The Evolution, Regulation, and Function of Placenta-Specific Genes","year":2008,"lang":"en","type":"review","venue":"Annual Review of Cell and Developmental Biology","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":224,"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","funders":"Canadian Institutes of Health Research","keywords":"Biology; Placenta; Gene; Gene family; Genetics; Function (biology); Gene expression","score_opus":0.012713991392023276,"score_gpt":0.25244370315883496,"score_spread":0.23972971176681168,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2146264881","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":[0.0007779368,0.996561,0.00032363483,0.00029435407,0.000121661695,0.0000029722032,0.00002403652,0.000012806977,0.0018814924],"genre_scores_gemma":[0.0023612939,0.9958931,0.00031084236,0.00010565657,0.00008886499,0.0000058967316,0.00003692737,0.0000020968057,0.0011952037],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.99986863,0.000021495985,0.000015348825,0.000035962286,0.000044888176,0.00001357352],"domain_scores_gemma":[0.9999238,0.000023487228,0.000014962459,0.0000041750077,0.000023789826,0.0000095944015],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00025542738,0.0005463132,0.000812954,0.001111567,0.00019294825,0.000654672,0.00053501554,0.00058791885,0.0010401377],"category_scores_gemma":[0.00029083414,0.00018393008,0.00016380734,0.0017326155,0.00052852696,0.00077662885,0.00040386926,0.0007121283,0.0014412681],"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":[0.00006778835,0.000022200978,0.000553918,0.007280512,0.00004525472,0.00055080303,0.00012136147,0.0005830186,0.012646627,0.0076369867,0.01541821,0.95507336],"study_design_scores_gemma":[0.000011222883,0.000053513457,0.003200328,0.0010532823,0.0000498573,0.0027699978,0.000100118275,0.00010032971,0.003025977,0.0030176183,0.98660153,0.000016235099],"about_ca_topic_score_codex":0.0008270745,"about_ca_topic_score_gemma":0.0006893398,"teacher_disagreement_score":0.001111567,"about_ca_system_score_codex":0.0007197411,"about_ca_system_score_gemma":0.0007112029,"threshold_uncertainty_score":0.005222082},"labels":[],"label_agreement":null},{"id":"W2146975401","doi":"10.1002/ajmg.b.30934","title":"Regionally reduced brain volume, altered serotonin neurochemistry, and abnormal behavior in mice null for the circadian rhythm output gene <i>Magel2</i>","year":2009,"lang":"en","type":"article","venue":"American Journal of Medical Genetics Part B Neuropsychiatric Genetics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","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":"University of Toronto; Hospital for Sick Children; University of Alberta","funders":"","keywords":"Circadian rhythm; Neurochemistry; Internal medicine; Endocrinology; Nucleus accumbens; Hypothalamus; Hippocampus; Neuroscience; Neurochemical; Amygdala; Biology; Dopamine; Medicine; Neurology","score_opus":0.010835415274824227,"score_gpt":0.2603576466815006,"score_spread":0.24952223140667634,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2146975401","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99203306,0.0009732192,0.0032157868,0.00015267725,0.0000424109,0.000020775822,0.0017909043,0.00036847984,0.0014026912],"genre_scores_gemma":[0.9868478,0.0008422031,0.0047963723,0.00012674299,0.0000252878,0.00008427217,0.0016684895,0.00023616824,0.0053727427],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99978226,0.000022853297,0.0000201128,0.00009422371,0.00005000567,0.000030469566],"domain_scores_gemma":[0.9996762,0.00003693951,0.00016247666,0.000021179323,0.000013862267,0.000089359906],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00012365902,0.000931018,0.00033068762,0.001306763,0.00021484637,0.00037015308,0.00034630045,0.000571353,0.002302118],"category_scores_gemma":[0.00014191616,0.00030551286,0.00028418587,0.00034101028,0.0008031004,0.00020395467,0.0003239608,0.000718523,0.0003094359],"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":[0.00017088183,0.00002941737,0.0006618458,0.000028532804,0.000020567524,0.00035621444,0.000037399263,0.00007362859,0.99731857,0.00014591926,0.00008916157,0.0010679913],"study_design_scores_gemma":[0.00012444402,0.0006056891,0.1091096,0.000028633345,0.00017821262,0.0075436444,0.00016612002,0.0017089421,0.8759758,0.00041361293,0.004102433,0.00004281951],"about_ca_topic_score_codex":0.0011978921,"about_ca_topic_score_gemma":0.0018722134,"teacher_disagreement_score":0.002302118,"about_ca_system_score_codex":0.00035222815,"about_ca_system_score_gemma":0.00020941933,"threshold_uncertainty_score":0.0077013373},"labels":[],"label_agreement":null},{"id":"W2148480736","doi":"10.1038/embor.2009.98","title":"Overgrowth of a mouse model of Simpson– Golabi–Behmel syndrome is partly mediated by Indian Hedgehog","year":2009,"lang":"en","type":"article","venue":"EMBO Reports","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":51,"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; Sunnybrook Health Science Centre","funders":"","keywords":"Hedgehog; Indian hedgehog; Hedgehog signaling pathway; Endocrinology; Biology; Internal medicine; Null allele; Mutant; Cell biology; Genetics; Signal transduction; Medicine; Gene","score_opus":0.007241860442712335,"score_gpt":0.223233290584847,"score_spread":0.21599143014213468,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2148480736","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9936748,0.0013445026,0.0017283516,0.00031363688,0.00008718357,0.000028600256,0.0009321077,0.00025036474,0.0016403568],"genre_scores_gemma":[0.9878498,0.0011095094,0.002286452,0.00011803419,0.000026349628,0.00005989234,0.0007481115,0.00013576081,0.0076660956],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9994099,0.000098661854,0.0000562911,0.00011052228,0.00020960886,0.000115074254],"domain_scores_gemma":[0.9991805,0.000099292985,0.00025664121,0.000098954566,0.00003435865,0.00033025583],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00026052576,0.0012846818,0.0005074651,0.0018343297,0.00035333855,0.00059875584,0.00048746943,0.0010554001,0.0027008115],"category_scores_gemma":[0.0002206316,0.0006696484,0.00069503207,0.0004090998,0.00078406616,0.0003783835,0.0006980081,0.0018119644,0.0008220197],"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":[0.00027405543,0.000054237604,0.00018907436,0.00002933054,0.000011305505,0.00036486788,0.000022051583,0.00006359635,0.9981629,0.00019569523,0.000066619046,0.0005662751],"study_design_scores_gemma":[0.00016341577,0.0005909071,0.0070207105,0.000027195598,0.00009480155,0.0027797066,0.00015654329,0.0016386231,0.9833907,0.00036124047,0.0037489468,0.00002707976],"about_ca_topic_score_codex":0.0013410163,"about_ca_topic_score_gemma":0.002193065,"teacher_disagreement_score":0.0027008115,"about_ca_system_score_codex":0.00045833585,"about_ca_system_score_gemma":0.0005019177,"threshold_uncertainty_score":0.0090351105},"labels":[],"label_agreement":null},{"id":"W2149392393","doi":"10.1534/genetics.107.081562","title":"Parental Effect of DNA (Cytosine-5) Methyltransferase 1 on Grandparental-Origin-Dependent Transmission Ratio Distortion in Mouse Crosses and Human Families","year":2008,"lang":"en","type":"article","venue":"Genetics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":14,"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 and Génome Québec Innovation Centre; Hospital for Sick Children; SickKids Foundation; University of Toronto; McGill University Health Centre; McGill University","funders":"Canadian Institutes of Health Research; Ontario Genomics; Ontario Genomics Institute; Genome Canada; McGill University","keywords":"Offspring; Allele; Biology; Genetics; Mendelian inheritance; Genotype; Meiotic drive; Gene; Pregnancy","score_opus":0.011777863219230357,"score_gpt":0.2620949342952634,"score_spread":0.25031707107603307,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2149392393","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9959728,0.0005880625,0.0018600076,0.00003328476,0.000007943778,0.000015760768,0.00023417828,0.0001014895,0.0011864512],"genre_scores_gemma":[0.9944364,0.0007145616,0.002664336,0.000030329573,0.000005336289,0.000020282347,0.00037411487,0.00006401645,0.001690639],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9994978,0.00015230551,0.000039322946,0.00016848653,0.00010295516,0.000039182643],"domain_scores_gemma":[0.9995945,0.00013251808,0.000120861216,0.00006495322,0.000016469075,0.00007074273],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00030316177,0.000563725,0.000304543,0.0011845033,0.00026145543,0.0002530596,0.00027945088,0.00031203253,0.0036689967],"category_scores_gemma":[0.00046031404,0.00038787062,0.0002582422,0.0003128117,0.0003522908,0.00012661841,0.0005160706,0.00036858104,0.00034961352],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0005216456,0.00007200923,0.004967157,0.000044047043,0.000055186603,0.001101716,0.000114210554,0.0001627525,0.98638374,0.00065743504,0.000084786625,0.0058353944],"study_design_scores_gemma":[0.0001403042,0.001227744,0.1030898,0.00004665498,0.00025270294,0.017494814,0.000115135816,0.0024734857,0.8681068,0.0005676543,0.0064311554,0.00005374531],"about_ca_topic_score_codex":0.0010231638,"about_ca_topic_score_gemma":0.0013665428,"teacher_disagreement_score":0.0036689967,"about_ca_system_score_codex":0.00027419862,"about_ca_system_score_gemma":0.00020261125,"threshold_uncertainty_score":0.012274027},"labels":[],"label_agreement":null},{"id":"W2149401378","doi":"10.1093/hmg/ddv159","title":"Progressive postnatal decline in leptin sensitivity of arcuate hypothalamic neurons in the<i>Magel2</i>-null mouse model of Prader–Willi syndrome","year":2015,"lang":"en","type":"article","venue":"Human Molecular Genetics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":43,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Women and Children’s Health Research Institute; University of Alberta","funders":"National Institutes of Health","keywords":"Leptin; Endocrinology; Internal medicine; Biology; Hypothalamus; Appetite; Leptin receptor; Obesity; Medicine","score_opus":0.030246119260698652,"score_gpt":0.2715109135179633,"score_spread":0.24126479425726466,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2149401378","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9923166,0.00075201265,0.0033042564,0.00029763972,0.000106061954,0.00006081397,0.0013353593,0.00039165287,0.0014356041],"genre_scores_gemma":[0.979512,0.0012457942,0.0064982744,0.0002609188,0.000046743462,0.00028770705,0.0014145321,0.00038116847,0.0103529375],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9995049,0.00004676005,0.00007532996,0.00015429841,0.00012609657,0.000092600545],"domain_scores_gemma":[0.9992544,0.00007686394,0.00026858744,0.000061042185,0.00004403573,0.00029492512],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.000338123,0.0010758876,0.0006289557,0.001151653,0.00035309204,0.0006662012,0.0007180606,0.0012781748,0.002956761],"category_scores_gemma":[0.00030384786,0.0006410344,0.0007331284,0.00029242563,0.001026394,0.00061657565,0.0005614675,0.0021423663,0.0010872275],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00022676904,0.00007002075,0.00019801513,0.00003055138,0.000008723274,0.00027322755,0.000039241055,0.000058859172,0.9984251,0.00013210102,0.00004252522,0.00049490994],"study_design_scores_gemma":[0.00015987037,0.0013645166,0.012557803,0.000042188352,0.00007135084,0.0029984757,0.0001752617,0.0019105413,0.97691125,0.00024241395,0.0035259943,0.000040299656],"about_ca_topic_score_codex":0.00090804877,"about_ca_topic_score_gemma":0.001179078,"teacher_disagreement_score":0.002956761,"about_ca_system_score_codex":0.0005355781,"about_ca_system_score_gemma":0.00032962748,"threshold_uncertainty_score":0.009891331},"labels":[],"label_agreement":null},{"id":"W2149922901","doi":"10.1136/jmg.2009.073189","title":"Assisted reproductive technologies do not enhance the variability of DNA methylation imprints in human","year":2009,"lang":"en","type":"article","venue":"Journal of Medical Genetics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":111,"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; Division of Materials Research","keywords":"GNAS complex locus; Differentially methylated regions; DNA methylation; Intracytoplasmic sperm injection; Methylation; Andrology; Epigenetics; Genomic imprinting; Biology; Pregnancy; In vitro fertilisation; Genetics; Medicine; DNA; Gene","score_opus":0.015872666162309954,"score_gpt":0.31207971366024956,"score_spread":0.2962070474979396,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2149922901","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99207836,0.0039706216,0.0010797201,0.000062561594,0.0000069282623,0.000008729542,0.00047976765,0.00001560168,0.0022976636],"genre_scores_gemma":[0.99830234,0.00075267674,0.00033249296,0.00003412962,0.0000074490126,0.000006209263,0.00021595575,0.000004349336,0.00034426287],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9997515,0.000068416804,0.000013879093,0.000060980543,0.00008161343,0.000023640743],"domain_scores_gemma":[0.9996538,0.00013100734,0.00012216411,0.000043662305,0.000027858963,0.000021510685],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00023244954,0.000084687876,0.00014486417,0.00037192486,0.000102954065,0.00026551087,0.00011825193,0.00012795499,0.0015514118],"category_scores_gemma":[0.0008874341,0.000081947765,0.00009246379,0.00041215698,0.0002831376,0.000080558304,0.00013086422,0.00009610168,0.00023885009],"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":[0.00073598407,0.00003403831,0.724121,0.00020023786,0.00032387854,0.00071828056,0.00069412217,0.0004085434,0.18496813,0.0010521091,0.00043900404,0.08630464],"study_design_scores_gemma":[0.000012291976,0.00039620433,0.96743304,0.00001577695,0.000078557576,0.0040377383,0.0001295566,0.00028434108,0.022382949,0.00043621025,0.0047873086,0.0000060154885],"about_ca_topic_score_codex":0.00057429005,"about_ca_topic_score_gemma":0.0007228571,"teacher_disagreement_score":0.0015514118,"about_ca_system_score_codex":0.00013520622,"about_ca_system_score_gemma":0.000098201795,"threshold_uncertainty_score":0.005190015},"labels":[],"label_agreement":null},{"id":"W2149956363","doi":"10.1093/nar/gkr871","title":"Tissue-specific alternative polyadenylation at the imprinted gene Mest regulates allelic usage at Copg2","year":2011,"lang":"en","type":"article","venue":"Nucleic Acids Research","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":24,"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":"Canadian Institutes of Health Research","keywords":"Biology; Genomic imprinting; Polyadenylation; Genetics; Allele; Locus (genetics); Gene; RNA interference; Imprinting (psychology); Regulation of gene expression; RNA; Gene expression; DNA methylation","score_opus":0.06589112043073807,"score_gpt":0.32226184858656487,"score_spread":0.2563707281558268,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2149956363","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99418145,0.00051200716,0.0036564139,0.000034657423,0.000016290256,0.000010049765,0.00024331147,0.0000929114,0.0012529937],"genre_scores_gemma":[0.9957475,0.0003119241,0.0017706091,0.000032491644,0.000006792638,0.000015638967,0.00034087908,0.0000458526,0.0017282715],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9999112,0.000009899836,0.0000073081933,0.000035728488,0.000021860975,0.000014090002],"domain_scores_gemma":[0.9998894,0.000020537838,0.00004219359,0.000014047646,0.000009115696,0.000024754658],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.000069950365,0.00028502702,0.000106611194,0.00014387205,0.00008741935,0.00022031629,0.0001552723,0.00013334815,0.00098467],"category_scores_gemma":[0.000113540365,0.00015661695,0.00015704494,0.00006540698,0.00017891005,0.000119940174,0.0002604587,0.0003057661,0.00035846792],"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":[0.000017495206,0.0000015816646,0.00014561087,0.000004704089,0.0000010832973,0.000026988091,0.0000038293356,0.000015643034,0.99945956,0.000035896566,0.0000058884343,0.00028162095],"study_design_scores_gemma":[0.0000072164244,0.000049119204,0.010582516,0.0000027445183,0.0000074508753,0.00020483794,0.000014743943,0.000702228,0.9873468,0.00003778047,0.0010417709,0.0000029708222],"about_ca_topic_score_codex":0.0002055287,"about_ca_topic_score_gemma":0.0005037553,"teacher_disagreement_score":0.00098467,"about_ca_system_score_codex":0.00019075368,"about_ca_system_score_gemma":0.000107042695,"threshold_uncertainty_score":0.0032940507},"labels":[],"label_agreement":null},{"id":"W2150199104","doi":"10.1098/rspb.2010.2627","title":"The evolutionary biology of child health","year":2011,"lang":"en","type":"review","venue":"Proceedings of the Royal Society B Biological Sciences","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","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":"Simon Fraser University","funders":"","keywords":"Biology; Epigenetics; Context (archaeology); Genomic imprinting; Offspring; Evolutionary developmental biology; Disease; Lineage (genetic); Human evolution; Developmental psychology; Evolutionary biology; Genetics; Gene; Psychology; Medicine; Pregnancy; DNA methylation","score_opus":0.043785028226027416,"score_gpt":0.3046800626499651,"score_spread":0.2608950344239377,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2150199104","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":[0.00011883192,0.9931252,0.00066910306,0.0021989308,0.0008834751,0.0000040414425,0.000009214643,0.000006748202,0.0029844383],"genre_scores_gemma":[0.0021885533,0.99369353,0.00043707376,0.0010248807,0.0011426383,0.000012435798,0.000013922812,0.0000037066204,0.0014832946],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.99959785,0.00014821145,0.00003421037,0.0000868893,0.00009288308,0.000040082043],"domain_scores_gemma":[0.9994161,0.00039249807,0.000044727258,0.00003044078,0.0000721239,0.00004424033],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0010060191,0.0011790466,0.0012635671,0.0027231781,0.00074906874,0.0019868985,0.0014467948,0.0034300555,0.003039983],"category_scores_gemma":[0.001529404,0.0003421272,0.00050958886,0.002486687,0.0050727925,0.0032175973,0.0018943417,0.0034695296,0.0013502731],"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":[0.000058212616,0.000052650383,0.0008105298,0.0069679557,0.00012838577,0.0004773507,0.00096966926,0.0013601562,0.0008154079,0.17082217,0.057236597,0.76030093],"study_design_scores_gemma":[0.000005878188,0.00003192061,0.0011464016,0.0027646173,0.000017030608,0.0008775213,0.00033858928,0.00012496147,0.0001453241,0.038143553,0.95638406,0.000020085761],"about_ca_topic_score_codex":0.0030641393,"about_ca_topic_score_gemma":0.0026287057,"teacher_disagreement_score":0.0034300555,"about_ca_system_score_codex":0.0025483998,"about_ca_system_score_gemma":0.0014045916,"threshold_uncertainty_score":0.018490016},"labels":[],"label_agreement":null},{"id":"W2151613979","doi":"10.1093/hmg/11.15.1743","title":"Identification and characterization of an imprinted antisense RNA (MESTIT1) in the human MEST locus on chromosome 7q32","year":2002,"lang":"en","type":"article","venue":"Human Molecular Genetics","topic":"Genetic Syndromes and Imprinting","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":"Hospital for Sick Children","funders":"RIKEN; Canadian Institutes of Health Research; Dunhill Medical Trust; Wellcome Trust; Howard Hughes Medical Institute","keywords":"Biology; Genomic imprinting; Genetics; Locus (genetics); Exon; Uniparental disomy; Molecular biology; Gene; Intron; Gene expression; Chromosome; Karyotype; DNA methylation","score_opus":0.015122352090671805,"score_gpt":0.25423701111710145,"score_spread":0.23911465902642964,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2151613979","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9937071,0.0006528761,0.004036196,0.00007015961,0.000017286822,0.000030402687,0.000750392,0.00005823085,0.00067737716],"genre_scores_gemma":[0.9851542,0.0006027248,0.0069811963,0.000109484885,0.000029595461,0.00004284874,0.0042609824,0.00004302432,0.002775898],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.99993134,0.0000035441608,0.000004862085,0.000030486288,0.000021239914,0.000008550739],"domain_scores_gemma":[0.9998658,0.000029361614,0.000040200677,0.000012890269,0.000012874323,0.000038943326],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00007136108,0.00028603233,0.00018336692,0.00024422584,0.00012578566,0.00018026332,0.00021736798,0.0002982236,0.0011059337],"category_scores_gemma":[0.00020747182,0.00023338204,0.00028391613,0.00013363775,0.00016137846,0.000101430385,0.0001425695,0.00027710685,0.0007446816],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00003871895,0.000005095044,0.00091873884,0.000023681629,0.0000037001716,0.0003284877,0.00001945829,0.00006347361,0.9974021,0.0000484707,0.000021617383,0.0011265376],"study_design_scores_gemma":[0.000054259002,0.0008013667,0.1028118,0.000026318436,0.00007449252,0.0075529534,0.000108313034,0.0029996377,0.8784191,0.00020526131,0.006921488,0.000025130259],"about_ca_topic_score_codex":0.00023727077,"about_ca_topic_score_gemma":0.00049077295,"teacher_disagreement_score":0.0011059337,"about_ca_system_score_codex":0.0001294237,"about_ca_system_score_gemma":0.00013284279,"threshold_uncertainty_score":0.00369972},"labels":[],"label_agreement":null},{"id":"W2153171596","doi":"10.1016/s1499-2671(09)33014-2","title":"Loss of the Prader-Willi Syndrome candidate gene Magel2 alters appetite energy balance","year":2009,"lang":"en","type":"article","venue":"Canadian Journal of Diabetes","topic":"Genetic Syndromes and Imprinting","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":true,"route_about_ca":false,"ca_institutions":"University of Alberta","funders":"","keywords":"Appetite; Medicine; Endocrinology; Circadian rhythm; Internal medicine; Insulin resistance; Obesity; Wakefulness; Candidate gene; Failure to thrive; Hypothalamus; Gene; Biology; Psychiatry; Genetics","score_opus":0.004081531698462292,"score_gpt":0.18517318805977248,"score_spread":0.1810916563613102,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2153171596","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9977837,0.00023753324,0.00085460395,0.0001243007,0.000058524292,0.000006068215,0.00023321899,0.00006354225,0.00063849246],"genre_scores_gemma":[0.99787736,0.00015157615,0.000449554,0.000052287487,0.0000073539177,0.000009401884,0.00010103853,0.00003955975,0.0013118637],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99981385,0.000043252872,0.000016102309,0.000044214572,0.00005110456,0.00003149427],"domain_scores_gemma":[0.99976355,0.00009129848,0.00006114579,0.000022955139,0.000010226061,0.000050755974],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00013745461,0.0004987376,0.00032233816,0.000546376,0.00021296003,0.0003479286,0.00036141687,0.0005798388,0.003256349],"category_scores_gemma":[0.00048522567,0.00026503135,0.00031079655,0.00020188329,0.00057180703,0.00016800496,0.00040054,0.000630317,0.00030957873],"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":[0.00090141327,0.000047369813,0.0024876646,0.000019599156,0.000054289718,0.0012388366,0.000046219877,0.00029256582,0.99245924,0.00026950162,0.00010988758,0.00207339],"study_design_scores_gemma":[0.0002711566,0.0005675754,0.10446519,0.000017792952,0.00030341744,0.008916787,0.00028872016,0.0041864538,0.87581676,0.00045743762,0.0046536545,0.000055074943],"about_ca_topic_score_codex":0.0016132785,"about_ca_topic_score_gemma":0.0019957277,"teacher_disagreement_score":0.003256349,"about_ca_system_score_codex":0.000261429,"about_ca_system_score_gemma":0.00032790334,"threshold_uncertainty_score":0.010893583},"labels":[],"label_agreement":null},{"id":"W2153415070","doi":"10.1093/hmg/9.12.1813","title":"Expression and imprinting of MAGEL2 suggest a role in Prader-Willi syndrome and the homologous murine imprinting phenotype","year":2000,"lang":"en","type":"article","venue":"Human Molecular Genetics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":159,"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":"University of Miami","keywords":"Imprinting (psychology); Biology; Genomic imprinting; In situ hybridization; Phenotype; Gene; Northern blot; Gene expression; Genetics; Central nervous system; Endocrinology; Molecular biology; DNA methylation","score_opus":0.0047517378301911856,"score_gpt":0.2183205789854818,"score_spread":0.21356884115529062,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2153415070","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9962842,0.0007294195,0.002013842,0.000055583125,0.000008735321,0.000003963006,0.00014021131,0.000040899813,0.00072317634],"genre_scores_gemma":[0.9956666,0.00032098236,0.001370875,0.000029968403,0.000007639941,0.000007609569,0.00034372514,0.0000089670675,0.0022436162],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9999434,0.000006833358,0.000003672803,0.0000245403,0.000011014863,0.000010534982],"domain_scores_gemma":[0.9999248,0.000011434595,0.00003080315,0.000007831058,0.000004221583,0.000021061647],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00006321775,0.0002968903,0.00012568147,0.00022523417,0.000083482984,0.00013129933,0.00016514369,0.00028059195,0.001130411],"category_scores_gemma":[0.0001276956,0.00012862585,0.0001779627,0.00007935425,0.00020842056,0.00015233006,0.0002325267,0.00027551097,0.00029277013],"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":[0.00008272901,0.000006307959,0.0020543127,0.00001769938,0.0000050760523,0.00074144336,0.000018428485,0.000081766986,0.9956079,0.0001771523,0.000013795798,0.0011934402],"study_design_scores_gemma":[0.000031128664,0.0003872158,0.23575152,0.0000138898,0.000050785267,0.010903103,0.00007036374,0.0019263142,0.7444783,0.00038921507,0.0059793177,0.000018873794],"about_ca_topic_score_codex":0.00024208507,"about_ca_topic_score_gemma":0.0004806313,"teacher_disagreement_score":0.001130411,"about_ca_system_score_codex":0.00012092134,"about_ca_system_score_gemma":0.00009832483,"threshold_uncertainty_score":0.003781557},"labels":[],"label_agreement":null},{"id":"W2153563181","doi":"10.1095/biolreprod.110.085480","title":"Side-by-Side Comparison of Five Commercial Media Systems in a Mouse Model: Suboptimal In Vitro Culture Interferes with Imprint Maintenance1","year":2010,"lang":"en","type":"article","venue":"Biology of Reproduction","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":208,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Children’s Health Research Institute; Western University","funders":"Institute of Gender and Health; Natural Sciences and Engineering Research Council of Canada; Canadian Institutes of Health Research; March of Dimes Foundation","keywords":"Genomic imprinting; Biology; Embryo culture; Imprinting (psychology); Blastocyst; Embryo; Epigenetics; DNA methylation; Andrology; Genetics; In vivo; Reproductive technology; Embryogenesis; Cell biology; Gene expression; Gene; Medicine","score_opus":0.012117768231121847,"score_gpt":0.2601739981159074,"score_spread":0.24805622988478557,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2153563181","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9914561,0.002645243,0.0033102927,0.00008805989,0.00014700608,0.0002454256,0.0010311545,0.000075129705,0.001001525],"genre_scores_gemma":[0.96802896,0.004160132,0.016780369,0.0002674047,0.00010295497,0.0009577026,0.003977045,0.00021447387,0.0055109872],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9981871,0.00045607827,0.00030960352,0.0003637873,0.00050959777,0.00017370594],"domain_scores_gemma":[0.9978672,0.00069979794,0.00053209806,0.00033860098,0.00027022435,0.00029194297],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0015974704,0.0010162189,0.0011791352,0.0015334389,0.00044324933,0.0007996419,0.00063532655,0.0010343776,0.0014900884],"category_scores_gemma":[0.0010976311,0.00039092908,0.001087608,0.0004892449,0.00068186026,0.00059396116,0.00071758614,0.0014462176,0.000421553],"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":[0.004231548,0.0011296774,0.0017918835,0.0002033335,0.000100481004,0.00017662485,0.00007894053,0.0003309364,0.987688,0.00010665406,0.00013443355,0.0040276037],"study_design_scores_gemma":[0.000098936005,0.015084675,0.0070849815,0.000021980924,0.0003220219,0.00030196967,0.00009083867,0.001281993,0.97340786,0.00007591448,0.002189732,0.000039115006],"about_ca_topic_score_codex":0.0012534431,"about_ca_topic_score_gemma":0.0023279241,"teacher_disagreement_score":0.0015974704,"about_ca_system_score_codex":0.00052934093,"about_ca_system_score_gemma":0.00038552994,"threshold_uncertainty_score":0.008448303},"labels":[],"label_agreement":null},{"id":"W2153779221","doi":"10.1136/jmg.39.2.81","title":"Current status of human chromosome 14","year":2002,"lang":"en","type":"review","venue":"Journal of Medical Genetics","topic":"Genetic Syndromes and Imprinting","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":"University of Alberta","funders":"Fondation pour la Recherche Médicale; University of Alberta; March of Dimes Foundation","keywords":"Genetics; Biology; Genomic imprinting; Chromosome; Gene map; Gene; Imprinting (psychology); Gene mapping; Chromosome 21; Karyotype; Epigenetics; Uniparental disomy; Human genome; Genetic marker; Chromosome 7 (human); Genome; DNA methylation","score_opus":0.05429683282768185,"score_gpt":0.37063017859228553,"score_spread":0.3163333457646037,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2153779221","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":[0.0003019744,0.994835,0.00027562576,0.0008635324,0.00053657254,0.0000054459006,0.000025206431,0.000021238176,0.0031353328],"genre_scores_gemma":[0.0015253896,0.9952684,0.0004092966,0.0004649481,0.00032748253,0.000008482924,0.0000915129,0.0000035997837,0.0019009397],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.9997124,0.00005554216,0.00003657847,0.0000553744,0.00011203498,0.000028083155],"domain_scores_gemma":[0.99964976,0.00013948516,0.00003969901,0.000016590648,0.0001166702,0.000037812482],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0007074,0.00081375765,0.0011987842,0.0017397394,0.0004118748,0.0011087571,0.00116393,0.0012346614,0.0070571997],"category_scores_gemma":[0.0009424441,0.00026013312,0.0003258475,0.0021053676,0.00082189986,0.0016956563,0.0008077933,0.0012791728,0.004122514],"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":[0.00010634022,0.000023094786,0.00026638975,0.0071303532,0.000034619956,0.00036842946,0.00009236259,0.00026978727,0.002783267,0.0063125542,0.032748017,0.94986475],"study_design_scores_gemma":[0.000009714192,0.000035239107,0.00046209412,0.0011832888,0.000028339406,0.00089754333,0.00006073484,0.000026717176,0.000497939,0.0016439614,0.99514526,0.00000915726],"about_ca_topic_score_codex":0.0019297777,"about_ca_topic_score_gemma":0.0017521332,"teacher_disagreement_score":0.0070571997,"about_ca_system_score_codex":0.0010260268,"about_ca_system_score_gemma":0.0021008772,"threshold_uncertainty_score":0.023608625},"labels":[],"label_agreement":null},{"id":"W2154296562","doi":"10.1002/gene.1077","title":"Imprinting defects in mouse embryos: stochastic errors or polymorphic phenotype?","year":2001,"lang":"en","type":"article","venue":"genesis","topic":"Genetic Syndromes and Imprinting","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":"McGill University Health Centre; Montreal Children's Hospital; Royal Victoria Hospital","funders":"","keywords":"Imprinting (psychology); Genomic imprinting; Biology; Embryo; Genetics; Phenotype; Carcinogenesis; Zygote; Gene; Embryogenesis; Gene expression; DNA methylation","score_opus":0.015466178723298314,"score_gpt":0.24311727330939673,"score_spread":0.22765109458609842,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2154296562","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9844908,0.0033274014,0.009758195,0.00017126973,0.000018546323,0.000021391235,0.0005507148,0.00021692686,0.0014447116],"genre_scores_gemma":[0.9945306,0.0015562964,0.0025862555,0.000051605155,0.000009414574,0.0000225119,0.00026112754,0.000036939007,0.0009452612],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9998235,0.000038126072,0.000023950446,0.00004644345,0.000040460593,0.000027533975],"domain_scores_gemma":[0.99970955,0.00006830949,0.000115118964,0.000058791855,0.000013618034,0.00003464653],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00024849412,0.00025434015,0.00017820485,0.0005040279,0.00008184203,0.00020483123,0.00017333956,0.0003430257,0.00076485483],"category_scores_gemma":[0.00034734662,0.00020251544,0.00016375752,0.0001912472,0.00026703384,0.00019135996,0.00018625702,0.0003094595,0.00024806472],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00012454673,0.000013341468,0.0040763817,0.000051530038,0.000015867776,0.00048124883,0.000044390756,0.00014989283,0.9896058,0.0006318945,0.000050276805,0.0047547617],"study_design_scores_gemma":[0.00005216869,0.00054590777,0.08831558,0.00004540965,0.00007563777,0.009364854,0.000068599045,0.0025005722,0.89248717,0.0014527523,0.005071645,0.000019811445],"about_ca_topic_score_codex":0.0002017934,"about_ca_topic_score_gemma":0.00033948492,"teacher_disagreement_score":0.00076485483,"about_ca_system_score_codex":0.00011001034,"about_ca_system_score_gemma":0.0000641763,"threshold_uncertainty_score":0.0025586486},"labels":[],"label_agreement":null},{"id":"W2155873540","doi":"10.1016/j.rbmo.2012.03.019","title":"The placental imprintome and imprinted gene function in the trophoblast glycogen cell lineage","year":2012,"lang":"en","type":"review","venue":"Reproductive BioMedicine Online","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":42,"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":"Genomic imprinting; Biology; Allele; Gene; Epigenetics; Genetics; Trophoblast; Imprinting (psychology); Lineage (genetic); Function (biology); Embryonic stem cell; Placenta; DNA methylation; Gene expression; Fetus","score_opus":0.023818092567878087,"score_gpt":0.29536693831677374,"score_spread":0.27154884574889565,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2155873540","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":[0.00019869779,0.9982754,0.00020098228,0.00031010047,0.0002085503,0.0000015232231,0.000016708073,0.0000064739547,0.00078154576],"genre_scores_gemma":[0.0014451471,0.99712116,0.0002536081,0.00014953632,0.0002446405,0.0000035813348,0.00003488274,0.0000017421852,0.0007456779],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.9998727,0.000022454871,0.000019491501,0.000024376648,0.00004739225,0.0000135150485],"domain_scores_gemma":[0.99979717,0.00009118964,0.000033971253,0.000008655075,0.000041901316,0.00002705987],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00056931394,0.000735603,0.0010601833,0.0013418607,0.00018513588,0.0008635301,0.00082459406,0.0010402714,0.0018219409],"category_scores_gemma":[0.00066000986,0.00029331326,0.00023583703,0.0014858815,0.00072351005,0.00096333574,0.00069319044,0.0012121854,0.00124366],"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":[0.00015605954,0.000031962867,0.00044772463,0.0067922156,0.00007334348,0.0007357098,0.00004550735,0.0004242383,0.0050565028,0.0070020924,0.02673335,0.95250124],"study_design_scores_gemma":[0.000027061526,0.000039297647,0.001525851,0.0011214615,0.00012192963,0.0028153574,0.000067244415,0.000121031306,0.0019059565,0.002689168,0.98954123,0.000024491503],"about_ca_topic_score_codex":0.0009927152,"about_ca_topic_score_gemma":0.0014777537,"teacher_disagreement_score":0.0018219409,"about_ca_system_score_codex":0.0007753777,"about_ca_system_score_gemma":0.0009441359,"threshold_uncertainty_score":0.006094992},"labels":[],"label_agreement":null},{"id":"W2157980542","doi":"10.1095/biolreprod.111.096602","title":"Loss of Genomic Imprinting in Mouse Embryos with Fast Rates of Preimplantation Development in Culture1","year":2012,"lang":"en","type":"article","venue":"Biology of Reproduction","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":97,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Children’s Health Research Institute; Western University","funders":"Institute of Gender and Health; Canadian Institutes of Health Research; Natural Sciences and Engineering Research Council of Canada; Children's Health Research Institute","keywords":"Genomic imprinting; Embryo; Biology; Imprinting (psychology); Embryogenesis; Andrology; Embryo culture; Genetics; Embryonic stem cell; Methylation; Inner cell mass; Blastocyst; Cell fate determination; Epigenetics; DNA methylation; Cell biology; Gene expression; Gene; Transcription factor","score_opus":0.01314233626520992,"score_gpt":0.2533268614587991,"score_spread":0.2401845251935892,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2157980542","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9698695,0.006680971,0.017714327,0.000094282,0.000053446158,0.000114730174,0.0027080674,0.000284489,0.0024801202],"genre_scores_gemma":[0.9727844,0.0032240804,0.013355085,0.00011416576,0.000024561237,0.00028208908,0.003643748,0.0001709479,0.0064008767],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99960023,0.00004260622,0.00006169361,0.00009563808,0.00013659225,0.00006320297],"domain_scores_gemma":[0.9995097,0.00015299911,0.00013880136,0.00010495458,0.000035099267,0.00005842756],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00041360816,0.00048248257,0.0003742834,0.00085207005,0.00022365316,0.00040111016,0.00047271562,0.00039786188,0.0010731319],"category_scores_gemma":[0.00032349725,0.0003953013,0.0005014206,0.00034170967,0.00023180463,0.00026515572,0.00030177963,0.0008983728,0.0007394024],"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":[0.000072217226,0.0000102250515,0.0008210934,0.00001756439,0.0000070951596,0.000051605515,0.000018658986,0.000038080452,0.9980769,0.00005005042,0.000015766977,0.00082067144],"study_design_scores_gemma":[0.000010838386,0.0003367947,0.03505088,0.000011704213,0.000036533707,0.0006142862,0.00002824353,0.000811993,0.96094304,0.000067714915,0.00207987,0.000008035531],"about_ca_topic_score_codex":0.0008510801,"about_ca_topic_score_gemma":0.0012122466,"teacher_disagreement_score":0.0010731319,"about_ca_system_score_codex":0.00033849632,"about_ca_system_score_gemma":0.00018579194,"threshold_uncertainty_score":0.0035899282},"labels":[],"label_agreement":null},{"id":"W2158230043","doi":"10.1093/carcin/bgp254","title":"Loss of imprinting of the insulin-like growth factor II (IGF2) gene in esophageal normal and adenocarcinoma tissues","year":2009,"lang":"en","type":"article","venue":"Carcinogenesis","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","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 Saskatchewan","funders":"Saskatchewan Health Research Foundation","keywords":"Imprinting (psychology); Internal medicine; Esophageal cancer; Genomic imprinting; Medicine; Gastroenterology; Insulin-like growth factor 2; Adenocarcinoma; Esophageal disease; Gene expression; Esophagus; Cancer; Growth factor; Biology; Gene; DNA methylation; Receptor","score_opus":0.00875851256152868,"score_gpt":0.2193568262374987,"score_spread":0.21059831367597,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2158230043","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99947053,0.00021531194,0.00013755044,0.0000034354416,0.0000012843051,0.0000023335294,0.00007256096,0.0000027038327,0.000094323594],"genre_scores_gemma":[0.9996567,0.000061071885,0.00008907432,0.0000038683556,0.00000163774,0.0000027228862,0.00012882665,0.0000012410198,0.000054820608],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9997969,0.000034649755,0.000022913406,0.000057130623,0.000043395674,0.00004500454],"domain_scores_gemma":[0.99949,0.00017721373,0.00015906998,0.000047115223,0.00004255974,0.00008398828],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00028359174,0.00016917977,0.0002970304,0.00060930726,0.00019724143,0.00034311402,0.00016301782,0.00015218764,0.00062972674],"category_scores_gemma":[0.0009352655,0.00019781041,0.00015062312,0.00044459707,0.00026846773,0.00020662294,0.00025591053,0.00019472232,0.00013034615],"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":[0.00035684803,0.0000126077775,0.989707,0.000011744381,0.00002439608,0.00056197797,0.00006160497,0.000051905787,0.0073081846,0.000010892938,0.000022383965,0.0018704457],"study_design_scores_gemma":[0.000006151315,0.00020274732,0.9946742,0.0000019942363,0.000021982809,0.0031360702,0.000093171526,0.00018045158,0.001498811,0.0000132963605,0.00016857852,0.0000024331812],"about_ca_topic_score_codex":0.0011905086,"about_ca_topic_score_gemma":0.0012329363,"teacher_disagreement_score":0.0011905086,"about_ca_system_score_codex":0.00020419301,"about_ca_system_score_gemma":0.0001235864,"threshold_uncertainty_score":0.0023670793},"labels":[],"label_agreement":null},{"id":"W2158310202","doi":"10.1111/j.0006-341x.2001.01074.x","title":"Statistical Analysis of Uniparental Disomy Data Using Hidden Markov Models","year":2001,"lang":"en","type":"article","venue":"Biometrics","topic":"Genetic Syndromes and Imprinting","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":"University of British Columbia","funders":"National Institutes of Health; Eunice Kennedy Shriver National Institute of Child Health and Human Development; National Institute for Health and Care Research; March of Dimes Foundation","keywords":"Nondisjunction; Uniparental disomy; Computer science; Crossover; Markov chain; Hidden Markov model; International HapMap Project; Set (abstract data type); Data set; Genetic genealogy; Chromosome; Genetics; Machine learning; Artificial intelligence; Biology; Single-nucleotide polymorphism; Genotype; Aneuploidy","score_opus":0.08566248651909217,"score_gpt":0.33077814357963814,"score_spread":0.24511565706054597,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2158310202","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":[0.14165626,0.00038133905,0.8549374,0.00040270863,0.000040339914,0.000120580655,0.001197666,0.0009830137,0.00028083098],"genre_scores_gemma":[0.815556,0.00037244995,0.1798502,0.00010424613,0.00007020065,0.00040729617,0.0029236386,0.00013170282,0.0005843322],"study_design_codex":"simulation_or_modeling","study_design_gemma":"simulation_or_modeling","domain_scores_codex":[0.99689984,0.001784209,0.00022255944,0.00055551605,0.00038341212,0.00015451288],"domain_scores_gemma":[0.95789135,0.03769693,0.001623915,0.001759199,0.00075587985,0.000272685],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.011994533,0.00059587054,0.00091007166,0.0014596184,0.0005085708,0.0010263851,0.0012011308,0.0006821098,0.0017177598],"category_scores_gemma":[0.026400443,0.000459042,0.0011872539,0.0011645477,0.0008354679,0.0011881392,0.00092605036,0.0017552761,0.00033027862],"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":[0.001509117,0.00046305012,0.1311574,0.0005405546,0.0021079937,0.0008604296,0.00089707016,0.5154299,0.012408639,0.053280994,0.003988133,0.2773568],"study_design_scores_gemma":[0.00003028051,0.00008552148,0.011297873,0.000015433283,0.00006831671,0.0000554836,0.00004813327,0.9637915,0.001389338,0.022735987,0.00045154482,0.000030524465],"about_ca_topic_score_codex":0.004344834,"about_ca_topic_score_gemma":0.0046792035,"teacher_disagreement_score":0.011994533,"about_ca_system_score_codex":0.00096877496,"about_ca_system_score_gemma":0.0010649033,"threshold_uncertainty_score":0.063433886},"labels":[],"label_agreement":null},{"id":"W2160062138","doi":"10.6000/2292-2598.2015.03.03.2","title":"Somatic Mosaicism as Modulator of the Global and Intellectual Phenotype in Epimutated Angelman Syndrome Patients","year":2015,"lang":"en","type":"article","venue":"Journal of Intellectual Disability - Diagnosis and Treatment","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":1,"is_retracted":false,"has_abstract":true,"route_ca_aff":false,"route_ca_fund":false,"route_ca_venue":true,"route_about_ca":false,"ca_institutions":"","funders":"Istituto Auxologico Italiano","keywords":"Angelman syndrome; UBE3A; Genomic imprinting; Genetics; Uniparental disomy; Imprinting (psychology); Biology; Allele; Intellectual disability; Chromosome 15; Multiplex ligation-dependent probe amplification; Neurodevelopmental disorder; DNA methylation; Chromosome; Gene; Ubiquitin ligase; Karyotype; Exon; Gene expression; Ubiquitin","score_opus":0.020153219625386146,"score_gpt":0.26101897959989867,"score_spread":0.24086575997451254,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2160062138","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9989526,0.00011835326,0.00028495662,0.000015991516,0.0000024420442,0.000007666742,0.00012091314,0.0000224563,0.000474556],"genre_scores_gemma":[0.99954754,0.00006485745,0.00012933451,0.000005583929,0.000003734955,0.0000025580284,0.000081350554,0.0000049004216,0.00016012802],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.999853,0.000017296274,0.000014943888,0.000055862565,0.000034517234,0.000024311883],"domain_scores_gemma":[0.99981004,0.000037002104,0.00006944885,0.00001313494,0.0000148125555,0.000055622277],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.000100477926,0.00037669644,0.00018369521,0.0009121795,0.00016657605,0.00023728231,0.00014500486,0.00022993317,0.0021274781],"category_scores_gemma":[0.0005805724,0.000116512216,0.00013959693,0.00040377956,0.0002392987,0.00011357816,0.0002658455,0.00012132894,0.00020079594],"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":[0.0011349455,0.00008991075,0.62138766,0.00009468894,0.0001114612,0.10791133,0.0013002465,0.00036363796,0.24102472,0.0005491414,0.00040976919,0.025622498],"study_design_scores_gemma":[0.000027596276,0.00042359353,0.7958807,0.000015321953,0.000094664516,0.18857308,0.00027023494,0.0006672538,0.012275784,0.00023535664,0.0015170001,0.00001950843],"about_ca_topic_score_codex":0.000537604,"about_ca_topic_score_gemma":0.000634208,"teacher_disagreement_score":0.0021274781,"about_ca_system_score_codex":0.00011947741,"about_ca_system_score_gemma":0.00009115271,"threshold_uncertainty_score":0.0071170926},"labels":[],"label_agreement":null},{"id":"W2160251268","doi":"10.1093/hmg/ddg194","title":"Insulator and silencer sequences in the imprinted region of human chromosome 11p15.5","year":2003,"lang":"en","type":"article","venue":"Human Molecular Genetics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":65,"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":"","keywords":"Silencer; Biology; CTCF; Imprinting (psychology); Genomic imprinting; CpG site; Enhancer; Gene; Genetics; Insulator (electricity); Locus (genetics); Promoter; Intron; DNA methylation; Gene expression","score_opus":0.0178322690328141,"score_gpt":0.26710147119353295,"score_spread":0.24926920216071885,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2160251268","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9914034,0.0024393029,0.0039104475,0.000087712084,0.000011233935,0.000008618155,0.00025155314,0.00006637773,0.0018212989],"genre_scores_gemma":[0.9958105,0.00048257562,0.0019696476,0.000045112818,0.000008465347,0.00000583474,0.0005724542,0.0000089927635,0.0010965463],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9998976,0.0000139883505,0.0000063035286,0.000029103334,0.00003447048,0.00001849432],"domain_scores_gemma":[0.99986565,0.00004145072,0.000044815155,0.000013719211,0.00000849124,0.000025922704],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00009667126,0.00014556633,0.00013526052,0.0002643709,0.000106400046,0.00016630498,0.00013471681,0.00013929949,0.0010309662],"category_scores_gemma":[0.0002584656,0.00013250411,0.00012539979,0.00013713661,0.00020256662,0.00009938901,0.00016677963,0.000151759,0.00031556716],"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":[0.0001706896,0.000009553361,0.0038965545,0.000051219093,0.000009635354,0.00055015116,0.000084032756,0.00015986615,0.9888741,0.0005589789,0.000052524203,0.005582637],"study_design_scores_gemma":[0.00007571025,0.0005755798,0.28519177,0.000057475016,0.000097433585,0.0056730215,0.00014975456,0.0020680304,0.6931992,0.0012270478,0.011665167,0.00001991885],"about_ca_topic_score_codex":0.00060885533,"about_ca_topic_score_gemma":0.0009652513,"teacher_disagreement_score":0.0010309662,"about_ca_system_score_codex":0.00016441607,"about_ca_system_score_gemma":0.00010179404,"threshold_uncertainty_score":0.0034489036},"labels":[],"label_agreement":null},{"id":"W2161157021","doi":"10.1210/en.2003-0591","title":"Defining Regulatory Regions in the Rat Prolactin Gene Family Locus Using a Large P1 Genomic Clone","year":2003,"lang":"en","type":"article","venue":"Endocrinology","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":8,"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 Manitoba","funders":"University of Manitoba","keywords":"Biology; Pseudogene; Gene; Placental lactogen; Prolactin; Locus (genetics); Gene family; genomic DNA; Genetics; clone (Java method); Trophoblast; Molecular biology; Gene expression; Placenta; Endocrinology; Fetus; Genome; Hormone","score_opus":0.016414296249345203,"score_gpt":0.25269235302295096,"score_spread":0.23627805677360575,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2161157021","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.97742826,0.0009531284,0.017448071,0.00015370268,0.000014989417,0.00010010928,0.0007529655,0.00020805495,0.0029407134],"genre_scores_gemma":[0.944795,0.002186511,0.03760365,0.00013028822,0.000032777276,0.000247191,0.007640347,0.00010754022,0.00725664],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9998926,0.00001281291,0.00000746285,0.000038546124,0.000026357337,0.000022155262],"domain_scores_gemma":[0.99982387,0.00006122756,0.000047440943,0.000015800466,0.000011892266,0.000039788556],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00009714736,0.00029284216,0.00015686743,0.00044536573,0.00015696874,0.00021937386,0.00022549136,0.0002040025,0.0013787748],"category_scores_gemma":[0.00027698826,0.00023744776,0.00022026524,0.0002134068,0.00026880633,0.0001506507,0.0002985075,0.00046513768,0.001008223],"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":[0.00005734401,0.0000141172295,0.0002416512,0.000021456517,0.0000012861775,0.00015054386,0.00003033615,0.000036384743,0.99629444,0.00013143272,0.000020273632,0.0030006696],"study_design_scores_gemma":[0.00013924156,0.0010421348,0.038355958,0.000068059235,0.000050567636,0.006100273,0.00016018537,0.0011464211,0.9339113,0.0005438369,0.018457891,0.000024152196],"about_ca_topic_score_codex":0.0008119986,"about_ca_topic_score_gemma":0.0010659823,"teacher_disagreement_score":0.0013787748,"about_ca_system_score_codex":0.00022686204,"about_ca_system_score_gemma":0.000338799,"threshold_uncertainty_score":0.004612446},"labels":[],"label_agreement":null},{"id":"W2161327979","doi":"10.1093/hmg/ddp379","title":"The interval between Ins2 and Ascl2 is dispensable for imprinting centre function in the murine Beckwith–Wiedemann region","year":2009,"lang":"en","type":"article","venue":"Human Molecular Genetics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":13,"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; Ontario Institute for Cancer Research; University of Toronto; University of British Columbia","funders":"Canadian Institutes of Health Research","keywords":"Genomic imprinting; Imprinting (psychology); Biology; Genetics; Epigenetics; Allele; Gene; DNA methylation; Gene expression","score_opus":0.0177984200042024,"score_gpt":0.26338588752506725,"score_spread":0.24558746752086485,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2161327979","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9953099,0.00062735274,0.0018021055,0.000051728748,0.00001833855,0.000009689234,0.00043293036,0.00013787282,0.0016100839],"genre_scores_gemma":[0.99289674,0.00030762737,0.0019030399,0.000030066274,0.000009815755,0.00002592755,0.0008443082,0.000071493974,0.0039110156],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9997484,0.000039896237,0.000031163272,0.00007082937,0.00006391728,0.000045886492],"domain_scores_gemma":[0.99948335,0.000044668286,0.00016986579,0.00004983906,0.000013474081,0.00023876547],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00016216868,0.00048367222,0.00020077317,0.0006399156,0.00022107379,0.00041378604,0.00036569565,0.00033528748,0.0021864148],"category_scores_gemma":[0.00014879477,0.00043424638,0.00024042706,0.00018136103,0.00043629698,0.000160166,0.00046953745,0.00047329586,0.0010305836],"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":[0.00017015624,0.000014897268,0.0004066056,0.000016156217,0.0000056388026,0.00018279244,0.000014766978,0.000084059466,0.9980902,0.00024725872,0.00003501962,0.00073248433],"study_design_scores_gemma":[0.00010783752,0.0004749512,0.028257085,0.000031768184,0.000042588683,0.002174261,0.00007890735,0.0015623501,0.95770293,0.00019213834,0.009354913,0.000020276337],"about_ca_topic_score_codex":0.0006180719,"about_ca_topic_score_gemma":0.0011644701,"teacher_disagreement_score":0.0021864148,"about_ca_system_score_codex":0.0002805355,"about_ca_system_score_gemma":0.00030301066,"threshold_uncertainty_score":0.0073143244},"labels":[],"label_agreement":null},{"id":"W2161352411","doi":"10.1128/mcb.01435-10","title":"An Extended Domain of <i>Kcnq1ot1</i> Silencing Revealed by an Imprinted Fluorescent Reporter","year":2011,"lang":"en","type":"article","venue":"Molecular and Cellular Biology","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":17,"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":"Canadian Institutes of Health Research","keywords":"Biology; Gene silencing; Genomic imprinting; DNA methylation; Reporter gene; Molecular biology; Transgene; Genetics; Green fluorescent protein; Gene; Gene expression","score_opus":0.00792062358987711,"score_gpt":0.22517100009757526,"score_spread":0.21725037650769816,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2161352411","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9837159,0.0007616627,0.011513527,0.00010141487,0.000029552391,0.000020532167,0.00063914916,0.00017407892,0.003044217],"genre_scores_gemma":[0.9908042,0.0003277138,0.003969866,0.00004282613,0.0000082482275,0.00002490362,0.0007548318,0.000047758323,0.0040197503],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9999088,0.000008376021,0.0000059258527,0.000031389944,0.000025738791,0.000019697236],"domain_scores_gemma":[0.99988854,0.0000152180255,0.000039116923,0.00001529409,0.000007151146,0.00003468358],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.000082435436,0.0002990738,0.00014248007,0.0001766454,0.00011215194,0.00019270573,0.00027082133,0.00023359955,0.0016689197],"category_scores_gemma":[0.00006272114,0.00014425766,0.00018995907,0.00010949147,0.000305149,0.00015392112,0.00025808907,0.0004904734,0.0005054515],"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":[0.000012735761,0.0000020710806,0.000050299193,0.000006256395,0.0000011172439,0.000028788063,0.000004636027,0.0000154826,0.99955434,0.00007776121,0.0000074779764,0.00023900594],"study_design_scores_gemma":[0.000006678475,0.00005840525,0.005382903,0.0000035002902,0.0000059986733,0.00045919843,0.0000096548465,0.0003291008,0.991559,0.000044702567,0.00213791,0.0000028411278],"about_ca_topic_score_codex":0.0007122644,"about_ca_topic_score_gemma":0.0013380151,"teacher_disagreement_score":0.0016689197,"about_ca_system_score_codex":0.00035458762,"about_ca_system_score_gemma":0.00020104,"threshold_uncertainty_score":0.0055831075},"labels":[],"label_agreement":null},{"id":"W2161588299","doi":"10.1186/1756-8935-4-7","title":"Extensive epigenetic reprogramming in human somatic tissues between fetus and adult","year":2011,"lang":"en","type":"article","venue":"Epigenetics & Chromatin","topic":"Genetic Syndromes and Imprinting","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":"Child and Family Research Institute; Pacific Centre for Reproductive Medicine; University of British Columbia","funders":"National Institutes of Health; Michael Smith Health Research BC; Canadian Institute for Advanced Research","keywords":"Reprogramming; Biology; Somatic cell; Epigenetics; Human genetics; Fetus; Epigenesis; Cell biology; Genetics; DNA methylation; Pregnancy; Gene; Gene expression","score_opus":0.023080123668449908,"score_gpt":0.2659722796408841,"score_spread":0.2428921559724342,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2161588299","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9854554,0.0039925515,0.0067077125,0.00007269105,0.000018837487,0.000030465564,0.0006876716,0.000066447785,0.0029683004],"genre_scores_gemma":[0.9954555,0.0009453737,0.002143237,0.000042330295,0.00000812544,0.000018095217,0.00059745094,0.0000120113245,0.00077792426],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.99986506,0.000018989442,0.000013024755,0.000046663732,0.00003922666,0.0000170893],"domain_scores_gemma":[0.9997757,0.000060451675,0.00006318905,0.00003737292,0.00003788598,0.000025435322],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00018389958,0.000116570016,0.00012944073,0.0003202311,0.00014229177,0.00023412198,0.00015611642,0.0001670432,0.0015015197],"category_scores_gemma":[0.0005368039,0.0000943302,0.00010067904,0.00021611585,0.0001874064,0.00011229909,0.000282997,0.00016272772,0.00033370385],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00046584036,0.000016791833,0.061030637,0.00014021681,0.00004402971,0.0009849565,0.0002702907,0.00015235494,0.90101177,0.00038148556,0.00013751212,0.035364076],"study_design_scores_gemma":[0.000025758718,0.0007695599,0.5587797,0.00005603202,0.000116279996,0.018607633,0.0004370671,0.00075446186,0.4078041,0.0006857086,0.011944843,0.0000189372],"about_ca_topic_score_codex":0.00051880564,"about_ca_topic_score_gemma":0.0004781589,"teacher_disagreement_score":0.0015015197,"about_ca_system_score_codex":0.00017738806,"about_ca_system_score_gemma":0.00016474121,"threshold_uncertainty_score":0.005023122},"labels":[],"label_agreement":null},{"id":"W2163441749","doi":"10.1002/ajmg.a.20370","title":"Unexpected death and critical illness in Prader–Willi syndrome: Report of ten individuals","year":2003,"lang":"en","type":"article","venue":"American Journal of Medical Genetics Part A","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":122,"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 Children's Hospital","funders":"","keywords":"Medicine; Demise; Pediatrics; Adrenal insufficiency; Autopsy; Intensive care medicine; Internal medicine","score_opus":0.012020472643480135,"score_gpt":0.29602827211050986,"score_spread":0.2840077994670297,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2163441749","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99878436,0.00021580014,0.00026985825,0.00008702301,0.000021089514,0.000028022321,0.000044210683,0.000009589091,0.00054002466],"genre_scores_gemma":[0.99854267,0.00031109684,0.00035199514,0.0000959703,0.000045564873,0.00002600081,0.00012699045,0.000005561583,0.00049406855],"study_design_codex":"observational","study_design_gemma":"case_report","domain_scores_codex":[0.9995536,0.00006077724,0.000055297845,0.000110828034,0.000076115146,0.00014334582],"domain_scores_gemma":[0.9990921,0.00015887375,0.00022261789,0.00006176171,0.000084029016,0.000380584],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00029344053,0.0009792023,0.00037808876,0.0012791704,0.0015329921,0.0005581564,0.0005203283,0.0009475933,0.0013300362],"category_scores_gemma":[0.002145099,0.00070058793,0.00042016088,0.00038389096,0.0010132533,0.00058011856,0.0012271928,0.0008487824,0.00034264015],"study_design_candidate":"case_report","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0002203302,0.00028051782,0.6492519,0.000059732356,0.00006159233,0.3320961,0.0038945093,0.00018332113,0.0025616596,0.00020867636,0.000916464,0.010265294],"study_design_scores_gemma":[0.000048437927,0.0014638859,0.37996233,0.000057477104,0.00008190972,0.61036044,0.0028801786,0.0004647836,0.0012369561,0.00022682783,0.0031253635,0.00009130145],"about_ca_topic_score_codex":0.003670646,"about_ca_topic_score_gemma":0.0035068095,"teacher_disagreement_score":0.003670646,"about_ca_system_score_codex":0.00052384584,"about_ca_system_score_gemma":0.00055779313,"threshold_uncertainty_score":0.007298529},"labels":[],"label_agreement":null},{"id":"W2164252048","doi":"10.1210/jc.2003-030222","title":"A Pituitary-Derived MEG3 Isoform Functions as a Growth Suppressor in Tumor Cells","year":2003,"lang":"en","type":"article","venue":"The Journal of Clinical Endocrinology & Metabolism","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":448,"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":"U.S. Public Health Service; National Institutes of Health; Jarislowsky Foundation; National Institute of Diabetes and Digestive and Kidney Diseases; Massachusetts General Hospital","keywords":"Pituitary tumors; Biology; Tumor suppressor gene; Corticotropic cell; Pituitary adenoma; Gene isoform; Cancer research; Ectopic expression; MEG3; Gene; Gene expression; Somatic cell; Pituitary gland; Adenoma; Molecular biology; Carcinogenesis; Genetics; Endocrinology; Downregulation and upregulation; Hormone","score_opus":0.022547382130748375,"score_gpt":0.3100039637456756,"score_spread":0.28745658161492726,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2164252048","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99570435,0.00085551856,0.0017820438,0.00010435556,0.000024244348,0.000008382122,0.00036687157,0.000048640955,0.001105676],"genre_scores_gemma":[0.99619883,0.00033210928,0.00103887,0.000027879234,0.000009115197,0.000008299822,0.00086600444,0.000015059037,0.001503822],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9999529,0.000005943785,0.0000038998733,0.000009806413,0.000016668993,0.000010724525],"domain_scores_gemma":[0.99991596,0.000023900224,0.000014431704,0.000013919236,0.000009593814,0.000022274611],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.000083395294,0.00018888045,0.0001249111,0.00016615108,0.0001533846,0.0002217686,0.00013444373,0.00015084144,0.0007054335],"category_scores_gemma":[0.00013591835,0.00008515717,0.00016534868,0.00012252506,0.00020894245,0.00012109823,0.00015683589,0.0002878815,0.00035661366],"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":[0.000046231646,0.0000028403867,0.00027119115,0.000005907726,0.0000010014857,0.00006731247,0.000006405331,0.000012841713,0.99909246,0.00007598866,0.000012981458,0.00040493332],"study_design_scores_gemma":[0.000021694077,0.0001449433,0.015571577,0.0000030797983,0.00001482823,0.001461199,0.00005442169,0.000655424,0.97723085,0.00020788562,0.004629745,0.0000043894906],"about_ca_topic_score_codex":0.0007412957,"about_ca_topic_score_gemma":0.0009977786,"teacher_disagreement_score":0.0007412957,"about_ca_system_score_codex":0.00025489094,"about_ca_system_score_gemma":0.00018552624,"threshold_uncertainty_score":0.002359867},"labels":[],"label_agreement":null},{"id":"W2164283721","doi":"10.1186/gb-2011-12-3-r25","title":"Genome-wide assessment of imprinted expression in human cells","year":2011,"lang":"en","type":"article","venue":"Genome biology","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":71,"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 and Génome Québec Innovation Centre","funders":"Canadian Institutes of Health Research; Canada Research Chairs; Genome Canada","keywords":"Biology; Human genetics; Genome Biology; Human genome; Genome; Computational biology; Genomic imprinting; Genetics; Genomics; Computational genomics; Personal genomics; Evolutionary biology; Gene expression; Gene; DNA methylation","score_opus":0.01911953228187124,"score_gpt":0.27028552359692853,"score_spread":0.2511659913150573,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2164283721","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.94110096,0.004357355,0.04427084,0.00008603702,0.000026011092,0.00009990974,0.00688078,0.0003753609,0.0028027128],"genre_scores_gemma":[0.966529,0.0016190828,0.02182268,0.00015765597,0.000018918472,0.00014862377,0.008507948,0.000064199405,0.0011317787],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9996222,0.00006106057,0.000021531658,0.00015665982,0.00010425876,0.000034169272],"domain_scores_gemma":[0.9997136,0.00011196238,0.000040415885,0.00006315151,0.000051951472,0.000018903509],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0003854816,0.0001515538,0.0002337575,0.00048620626,0.00014363862,0.00039235866,0.00015723538,0.0002894709,0.0011327307],"category_scores_gemma":[0.00042484025,0.000107037195,0.00016693349,0.00062575185,0.00016701182,0.00006970127,0.0002037459,0.00024154672,0.0005284423],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0001936586,0.000025946245,0.026546225,0.00010694293,0.00009713965,0.00013308437,0.00011942411,0.00026012113,0.96026915,0.00012534365,0.00019377258,0.011929197],"study_design_scores_gemma":[0.000024463085,0.00044022157,0.31900093,0.000029479339,0.00025062516,0.0020201304,0.00013968915,0.002348305,0.6628401,0.0003621409,0.012523428,0.000020446867],"about_ca_topic_score_codex":0.0005252856,"about_ca_topic_score_gemma":0.00077997043,"teacher_disagreement_score":0.0011327307,"about_ca_system_score_codex":0.00011562327,"about_ca_system_score_gemma":0.00014765869,"threshold_uncertainty_score":0.0037893653},"labels":[],"label_agreement":null},{"id":"W2164504762","doi":"10.1002/ajmg.a.32332","title":"Beckwith‐Wiedemann syndrome in adults: Observations from one family and recommendations for care","year":2008,"lang":"en","type":"review","venue":"American Journal of Medical Genetics Part A","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":23,"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","funders":"","keywords":"Malignancy; Medicine; Beckwith–Wiedemann syndrome; Infertility; Pediatrics; Pregnancy; Internal medicine","score_opus":0.05160115333471197,"score_gpt":0.3286387192876364,"score_spread":0.2770375659529244,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2164504762","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":[0.0010670284,0.99077576,0.00065762043,0.003982508,0.00079278415,0.000013457934,0.000041838124,0.00003212886,0.0026368664],"genre_scores_gemma":[0.0038512803,0.99189526,0.0011898853,0.0013881371,0.0006359966,0.000014779749,0.00006995632,0.0000035515875,0.00095112785],"study_design_codex":"design_other","study_design_gemma":"case_report","domain_scores_codex":[0.9997762,0.000045870263,0.00005604257,0.000033408553,0.00006971266,0.000018758505],"domain_scores_gemma":[0.99962056,0.00016855093,0.00005884664,0.000012440981,0.00008900394,0.000050535346],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00051172863,0.0007291961,0.0011913112,0.0014949399,0.0003520395,0.0006752116,0.0009395056,0.0016476397,0.001339942],"category_scores_gemma":[0.001407601,0.00021732549,0.0003483493,0.0013043581,0.00039613352,0.001357925,0.0004488146,0.001536509,0.0010899933],"study_design_candidate":"case_report","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.000059956423,0.000056682176,0.0036058933,0.005726303,0.000091075926,0.023814002,0.00027009263,0.00024827346,0.00074086693,0.0014263258,0.08705038,0.8769102],"study_design_scores_gemma":[0.00006004292,0.00013126316,0.01329129,0.014957744,0.00045182195,0.22474624,0.0011082172,0.00023233569,0.00051241997,0.0042357324,0.74018925,0.00008363973],"about_ca_topic_score_codex":0.0020394314,"about_ca_topic_score_gemma":0.0045916247,"teacher_disagreement_score":0.0020394314,"about_ca_system_score_codex":0.00049503124,"about_ca_system_score_gemma":0.0009880089,"threshold_uncertainty_score":0.0044825673},"labels":[],"label_agreement":null},{"id":"W2164643560","doi":"10.1152/physiolgenomics.00071.2005","title":"Genome-wide analysis of gene transcription in the hypothalamus","year":2005,"lang":"en","type":"article","venue":"Physiological Genomics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":16,"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":"Canadian Institutes of Health Research","keywords":"Biology; Gene; Genetics; Candidate gene; Phenotype; Human genome; Genome; Gene expression; Hypothalamus; Population; Gene expression profiling; Computational biology; Neuroscience; Medicine","score_opus":0.02244686644299496,"score_gpt":0.23842578624586838,"score_spread":0.21597891980287343,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2164643560","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99592507,0.00065221044,0.0020948362,0.000037234127,0.0000035981861,0.00000823158,0.0009030717,0.000035316734,0.0003404543],"genre_scores_gemma":[0.99224734,0.0005082125,0.0044797976,0.00007275764,0.000008694609,0.000025052932,0.0022193016,0.000016341575,0.00042243983],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9998704,0.000022041328,0.000005182163,0.000059724567,0.000029631772,0.000012933958],"domain_scores_gemma":[0.99991083,0.000033846336,0.000026818125,0.000006789724,0.000009064485,0.000012597063],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00016991177,0.00011101123,0.00022032406,0.00048726247,0.00012057431,0.0002224732,0.00008704328,0.0001386409,0.00043550186],"category_scores_gemma":[0.00018417086,0.000095500574,0.00019406433,0.00032962908,0.00015438192,0.000051085633,0.00013910861,0.0002179127,0.00009631176],"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":[0.0003888483,0.000020493395,0.01985061,0.000044645814,0.0000686413,0.00011039096,0.000059373902,0.0003807513,0.97318673,0.000101224345,0.00008668074,0.00570148],"study_design_scores_gemma":[0.000050010993,0.00026570886,0.894752,0.000010070634,0.00013264334,0.0008443808,0.00010387948,0.003106176,0.09830435,0.0002914281,0.0021231892,0.000016049207],"about_ca_topic_score_codex":0.0009459912,"about_ca_topic_score_gemma":0.0017673764,"teacher_disagreement_score":0.0009459912,"about_ca_system_score_codex":0.00012613962,"about_ca_system_score_gemma":0.00012527729,"threshold_uncertainty_score":0.0018809438},"labels":[],"label_agreement":null},{"id":"W2164748186","doi":"10.1186/1471-2156-6-s1-s159","title":"A simple nonparametric multipoint procedure to test for linkage through mothers or fathers as well as imprinting effects in the presence of linkage","year":2005,"lang":"en","type":"article","venue":"BMC Genetics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":7,"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 and Génome Québec Innovation Centre; McGill Genome Centre; McGill University Health Centre","funders":"Canadian Institutes of Health Research","keywords":"Imprinting (psychology); Genetic linkage; Genetics; Biology; Linkage (software); Genomic imprinting; Nonparametric statistics; Null hypothesis; Gene; Candidate gene; Statistical hypothesis testing; Evolutionary biology; Statistics; Mathematics","score_opus":0.016057938750947385,"score_gpt":0.29067779830599755,"score_spread":0.27461985955505014,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2164748186","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":[0.027313083,0.00013231987,0.96334845,0.000101229714,0.00015033396,0.0010862072,0.0022753652,0.0037083614,0.0018846438],"genre_scores_gemma":[0.11142276,0.00011584747,0.87452614,0.00016860063,0.000079004116,0.005728367,0.0026701516,0.0016677207,0.0036213857],"study_design_codex":"design_other","study_design_gemma":"theoretical_or_conceptual","domain_scores_codex":[0.9867111,0.0066839918,0.0008589203,0.0024161453,0.0028034796,0.0005263992],"domain_scores_gemma":[0.95107836,0.032146227,0.0025426587,0.011617823,0.001996148,0.00061878597],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.015431637,0.001284803,0.0022136413,0.0029768718,0.0014574273,0.0013176535,0.0028484722,0.0017026544,0.024349133],"category_scores_gemma":[0.056611307,0.0007378099,0.0027073054,0.0026355905,0.0022273818,0.001288137,0.0032323368,0.003297059,0.0035505667],"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":[0.002632525,0.0009757418,0.07443856,0.0017291033,0.0034213415,0.0025020617,0.0011845618,0.015990471,0.05118116,0.039649565,0.030984977,0.77531004],"study_design_scores_gemma":[0.001833881,0.0060975654,0.28597015,0.00060622545,0.0020090998,0.0116454465,0.0010100169,0.32169816,0.08123968,0.14533341,0.14163658,0.0009198431],"about_ca_topic_score_codex":0.0016857241,"about_ca_topic_score_gemma":0.0024091136,"teacher_disagreement_score":0.024349133,"about_ca_system_score_codex":0.0006517743,"about_ca_system_score_gemma":0.0021070824,"threshold_uncertainty_score":0.081611276},"labels":[],"label_agreement":null},{"id":"W2164973887","doi":"10.1371/journal.pgen.1001251","title":"Thymus-Associated Parathyroid Hormone Has Two Cellular Origins with Distinct Endocrine and Immunological Functions","year":2010,"lang":"en","type":"article","venue":"PLoS Genetics","topic":"Genetic Syndromes and Imprinting","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":"Memorial University of Newfoundland","funders":"Eunice Kennedy Shriver National Institute of Child Health and Human Development; Medical Research Council; National Institutes of Health; National Institute of Allergy and Infectious Diseases; Deutsches Krebsforschungszentrum; Leukemia and Lymphoma Society","keywords":"Biology; Parathyroid hormone; Internal medicine; Endocrinology; Parathyroid chief cell; Parathyroid gland; Homeostasis; Organogenesis; Endocrine system; Hormone; Calcium; Gene; Genetics; Medicine","score_opus":0.013944757147507127,"score_gpt":0.21808840830861723,"score_spread":0.2041436511611101,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2164973887","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9464448,0.020669563,0.026740205,0.0002414122,0.00011469818,0.000069999616,0.0007019967,0.00022586629,0.0047914423],"genre_scores_gemma":[0.98391956,0.0039315345,0.0073118717,0.00011350273,0.00007025454,0.000042176747,0.0007686937,0.0000447888,0.003797593],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9997012,0.000018002556,0.000025757487,0.00008318235,0.00011917673,0.000052675867],"domain_scores_gemma":[0.99959725,0.000056681085,0.00009941685,0.00006564194,0.0000691831,0.000111772584],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00021411832,0.00039431805,0.00041596856,0.00049739954,0.00022920078,0.00079547294,0.00044448776,0.0004026178,0.0011318782],"category_scores_gemma":[0.00029120676,0.00021578146,0.00052317494,0.0002351533,0.00033554184,0.00045307385,0.0007580727,0.00068891264,0.0003998537],"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":[0.00010504686,0.000008562306,0.0016745734,0.00008073456,0.00000894133,0.00021681585,0.000046237128,0.00002343975,0.99328244,0.00051059446,0.000025791202,0.0040167114],"study_design_scores_gemma":[0.00004565138,0.0004208517,0.0676232,0.000038818198,0.00011608951,0.005692199,0.00013748236,0.0008623626,0.9115692,0.0006054372,0.012846341,0.000042411306],"about_ca_topic_score_codex":0.00036183267,"about_ca_topic_score_gemma":0.0004358235,"teacher_disagreement_score":0.0011318782,"about_ca_system_score_codex":0.00028646216,"about_ca_system_score_gemma":0.00025184097,"threshold_uncertainty_score":0.0037865639},"labels":[],"label_agreement":null},{"id":"W2165425175","doi":"10.1016/j.devcel.2009.12.017","title":"ATRX Partners with Cohesin and MeCP2 and Contributes to Developmental Silencing of Imprinted Genes in the Brain","year":2010,"lang":"en","type":"article","venue":"Developmental Cell","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":178,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Lawson Health Research Institute; University Health Network; Western University; Children’s Health Research Institute; Mental Health Commission of Canada","funders":"Natural Sciences and Engineering Research Council of Canada; Canadian Institutes of Health Research; International Rett Syndrome Foundation","keywords":"Biology; Genomic imprinting; ATRX; Gene silencing; Cohesin; MECP2; Genetics; Gene; Cell biology; Meiosis; DNA methylation; Mutation; Phenotype; Gene expression","score_opus":0.0060567624258092605,"score_gpt":0.2207533121127046,"score_spread":0.21469654968689533,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2165425175","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.98832613,0.004153427,0.003418535,0.00030890532,0.000041404135,0.0000055268833,0.00014048391,0.00015760213,0.0034480768],"genre_scores_gemma":[0.99425274,0.0006415068,0.0006751526,0.00003938641,0.000011808443,0.0000029586438,0.00013176656,0.00002932034,0.0042152936],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99982506,0.000021413167,0.000012498508,0.00003782929,0.00006143123,0.000041810876],"domain_scores_gemma":[0.99982125,0.000016938871,0.00005728877,0.000024040919,0.00001645286,0.000063993306],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00016265047,0.00032351358,0.00025580393,0.00044982496,0.0002812272,0.0007465837,0.00046607526,0.0003400317,0.0021563752],"category_scores_gemma":[0.00022492211,0.000330313,0.00018471076,0.00017411995,0.00037368305,0.0004327474,0.00066020264,0.00047062268,0.00085965346],"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":[0.00014200038,0.000013552878,0.0018436379,0.00002966223,0.000027206877,0.00087730447,0.000020200896,0.00019904226,0.9929737,0.00082230085,0.00016424018,0.0028870595],"study_design_scores_gemma":[0.000030296344,0.00007861931,0.043683294,0.000008794325,0.000059085425,0.004815783,0.00010564564,0.0024763923,0.9437289,0.00066513784,0.004335821,0.000012301906],"about_ca_topic_score_codex":0.00059837813,"about_ca_topic_score_gemma":0.0010338638,"teacher_disagreement_score":0.0021563752,"about_ca_system_score_codex":0.00029945842,"about_ca_system_score_gemma":0.00022906576,"threshold_uncertainty_score":0.0072137713},"labels":[],"label_agreement":null},{"id":"W2165496628","doi":"10.1242/dev.057778","title":"Depletion of <i>Kcnq1ot1</i> non-coding RNA does not affect imprinting maintenance in stem cells","year":2011,"lang":"en","type":"article","venue":"Development","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":62,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Children’s Health Research Institute; Lawson Health Research Institute; Western University","funders":"Institute of Gender and Health; National Institutes of Health; National Cancer Institute; Natural Sciences and Engineering Research Council of Canada; Canadian Institutes of Health Research; Lawson Health Research Institute","keywords":"Biology; Genomic imprinting; Non-coding RNA; DNA methylation; Embryonic stem cell; Gene silencing; Gene; Genetics; Imprinting (psychology); Epigenetics; RNA; microRNA; Long non-coding RNA; Transcription (linguistics); Regulation of gene expression; Cell biology; Gene expression","score_opus":0.015480516245157524,"score_gpt":0.21382991729323395,"score_spread":0.1983494010480764,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2165496628","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9930969,0.0008323189,0.0033860493,0.00008624759,0.000038902315,0.000033750443,0.00082302425,0.00012969405,0.0015729595],"genre_scores_gemma":[0.9932661,0.00038470887,0.001666719,0.000082095205,0.000005930204,0.00004440495,0.0012676175,0.00005084866,0.0032315399],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9997844,0.00001841697,0.00003100899,0.00005890413,0.00006772288,0.000039618877],"domain_scores_gemma":[0.9996394,0.00009614627,0.0000902028,0.000044071396,0.000032478827,0.00009765757],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0001848006,0.00027825398,0.0002825174,0.00017682133,0.00013702328,0.00034033819,0.0003035774,0.00027518597,0.0013806302],"category_scores_gemma":[0.00017967884,0.000175761,0.00023153647,0.00009718562,0.0003238731,0.00021686805,0.00014758663,0.0005667439,0.00041985617],"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":[0.000034581008,0.000008476703,0.0001602617,0.000013697657,0.0000029740197,0.000018298646,0.000010096311,0.00004420309,0.99928635,0.000056369496,0.000013272034,0.00035143335],"study_design_scores_gemma":[0.0000066628836,0.0001011817,0.0032002162,0.0000028668267,0.000009896756,0.00007055925,0.000017413764,0.0005552978,0.99493414,0.000022959484,0.0010764758,0.0000023857187],"about_ca_topic_score_codex":0.0011765665,"about_ca_topic_score_gemma":0.0017935596,"teacher_disagreement_score":0.0013806302,"about_ca_system_score_codex":0.00043603484,"about_ca_system_score_gemma":0.00032903315,"threshold_uncertainty_score":0.0046186447},"labels":[],"label_agreement":null},{"id":"W2166152082","doi":"10.1210/jc.2012-3888","title":"Growth Hormone Research Society Workshop Summary: Consensus Guidelines for Recombinant Human Growth Hormone Therapy in Prader-Willi Syndrome","year":2013,"lang":"en","type":"review","venue":"The Journal of Clinical Endocrinology & Metabolism","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":380,"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 Universitaire Sainte-Justine","funders":"Cliniques Universitaires Saint-Luc; Children's Hospital of Pittsburgh; National Institute of Diabetes and Digestive and Kidney Diseases; Erasmus Universitair Medisch Centrum Rotterdam; Sahlgrenska Akademin; Medical Research Council; Centre hospitalier universitaire Sainte-Justine; Istituto Auxologico Italiano; National Institutes of Health; Massachusetts General Hospital; Istituto Ortopedico Rizzoli di Bologna; Institut National de la Santé et de la Recherche Médicale; University of New South Wales; Aarhus Universitetshospital; Johns Hopkins Children's Center; Imperial College London; Helsingin Yliopisto; Novo Nordisk; Aarhus Universitet; Göteborgs Universitet; McMaster University; University of Sydney; Johns Hopkins University; Foundation for Prader-Willi Research; Hospital for Sick Children; Université de Montréal; Pfizer; Eli Lilly and Company","keywords":"Human growth hormone; Recombinant DNA; Growth hormone; Hormone therapy; Hormone; Medicine; Endocrinology; Internal medicine; Biology; Biochemistry; Gene","score_opus":0.32844551305299874,"score_gpt":0.4977400659301458,"score_spread":0.16929455287714706,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2166152082","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":[0.0021232292,0.3151797,0.021673787,0.54202694,0.062474582,0.010827813,0.011511267,0.0006905917,0.033492032],"genre_scores_gemma":[0.025115157,0.47566953,0.18776539,0.18377513,0.029725423,0.029482463,0.03725026,0.0006954047,0.030521305],"study_design_codex":"not_applicable","study_design_gemma":"not_applicable","domain_scores_codex":[0.9593524,0.017530745,0.013527802,0.0015459079,0.006736754,0.001306353],"domain_scores_gemma":[0.91146845,0.021659719,0.011015512,0.0020324509,0.04956801,0.004255847],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0604573,0.0020423848,0.0037960478,0.008899473,0.0017372825,0.0046587237,0.0087243235,0.011263541,0.009244264],"category_scores_gemma":[0.08482902,0.0012376874,0.008196212,0.005803096,0.0017487304,0.0032719683,0.005536918,0.011112383,0.0089526065],"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":[0.00023323059,0.00014918362,0.0008348808,0.028824488,0.00037194655,0.0005592366,0.0007291672,0.0006458437,0.0009952913,0.0039853645,0.7384759,0.22419545],"study_design_scores_gemma":[0.00038153838,0.00011749335,0.0026750392,0.10554419,0.00067037856,0.001037875,0.0005579755,0.00035606016,0.00053475436,0.00552997,0.8824858,0.000109008295],"about_ca_topic_score_codex":0.008808377,"about_ca_topic_score_gemma":0.008181294,"teacher_disagreement_score":0.0604573,"about_ca_system_score_codex":0.00706093,"about_ca_system_score_gemma":0.03949753,"threshold_uncertainty_score":0.3197326},"labels":[],"label_agreement":null},{"id":"W2167980095","doi":"10.1016/j.ajpath.2011.07.002","title":"Silencing of the Imprinted DLK1-MEG3 Locus in Human Clinically Nonfunctioning Pituitary Adenomas","year":2011,"lang":"en","type":"article","venue":"American Journal Of Pathology","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":95,"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 Institutes of Health; Jarislowsky Foundation","keywords":"MEG3; Gene silencing; Genomic imprinting; Cancer research; Medicine; Biology; Genetics; Gene; DNA methylation; RNA","score_opus":0.013938040122147638,"score_gpt":0.25486389720499514,"score_spread":0.2409258570828475,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2167980095","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9982698,0.00042124907,0.0003402726,0.00005103785,0.000007270843,0.0000046716773,0.00016950686,0.000019901117,0.00071631704],"genre_scores_gemma":[0.9995197,0.000073808405,0.00008337117,0.000008412701,0.0000021811136,0.000002272158,0.00009992774,0.0000057578086,0.00020468714],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99987555,0.000019947905,0.000014296125,0.000027006356,0.0000370982,0.000026106749],"domain_scores_gemma":[0.99971384,0.00012851962,0.000046203524,0.000033105873,0.00002481204,0.00005342637],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00013230374,0.00022207222,0.00029294044,0.0007223216,0.00039998183,0.00042324176,0.00020114836,0.00024729394,0.0010663702],"category_scores_gemma":[0.00046063273,0.00017415333,0.0001917426,0.00035252128,0.00046256738,0.00009893059,0.00028548008,0.00022894546,0.00021395324],"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":[0.0006174109,0.000022571861,0.01701382,0.0000373662,0.000020049232,0.0063074874,0.00028197895,0.00019075847,0.9721644,0.0002890146,0.000118537166,0.0029365008],"study_design_scores_gemma":[0.00016901255,0.0005575071,0.43803972,0.000011384495,0.00018740955,0.051262233,0.0012926143,0.0024273053,0.49902642,0.0011297432,0.005847162,0.000049581573],"about_ca_topic_score_codex":0.0036472587,"about_ca_topic_score_gemma":0.0036070512,"teacher_disagreement_score":0.0036472587,"about_ca_system_score_codex":0.00049379887,"about_ca_system_score_gemma":0.00029494532,"threshold_uncertainty_score":0.007252097},"labels":[],"label_agreement":null},{"id":"W2168910284","doi":"10.1093/nar/gkh671","title":"Tissue-specific and imprinted epigenetic modifications of the human NDN gene","year":2004,"lang":"en","type":"article","venue":"Nucleic Acids Research","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":51,"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":"Natural Sciences and Engineering Research Council of Canada; Alberta Heritage Foundation for Medical Research; Fondation pour la Recherche Médicale; Canadian Institutes of Health Research; University of Miami","keywords":"Biology; Epigenetics of physical exercise; Epigenetics; Cancer epigenetics; DNA methylation; Epigenomics; Histone methylation; Histone; Epigenetic regulation of neurogenesis; Histone code; Histone H2A; Genetics; Genomic imprinting; Molecular biology; Histone methyltransferase; Gene; Gene expression; Nucleosome","score_opus":0.048756542291033524,"score_gpt":0.3367287096033134,"score_spread":0.28797216731227987,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2168910284","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99260604,0.0012371943,0.0044449717,0.00004455537,0.000010274674,0.000008384642,0.00028346071,0.000023232064,0.0013420015],"genre_scores_gemma":[0.9960549,0.00042432762,0.0016334299,0.000017943086,0.0000032443622,0.000007748508,0.00036254383,0.0000064073665,0.0014894408],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9999398,0.0000067515134,0.0000035956496,0.000024328954,0.000018162385,0.0000074486684],"domain_scores_gemma":[0.99992967,0.000018681203,0.000016621681,0.000016692788,0.0000071960662,0.00001121048],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00007390612,0.00008504444,0.00007363346,0.00011272437,0.000058738675,0.00011960553,0.000091139416,0.00008645882,0.00085737236],"category_scores_gemma":[0.00025806422,0.00007732597,0.00007397967,0.00007949558,0.0001606429,0.000099912875,0.000110188405,0.00012330542,0.00018414205],"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":[0.0001028782,0.000005609884,0.005679573,0.000026861373,0.000009522335,0.00013852675,0.00003167202,0.00015020269,0.9861391,0.00023577166,0.000024262552,0.007456055],"study_design_scores_gemma":[0.000023464252,0.00018285564,0.2759976,0.000010081931,0.000032794836,0.0028948274,0.0000598927,0.0018012357,0.713246,0.00054886594,0.0051914216,0.000010961182],"about_ca_topic_score_codex":0.000788243,"about_ca_topic_score_gemma":0.0023490654,"teacher_disagreement_score":0.00085737236,"about_ca_system_score_codex":0.00021170039,"about_ca_system_score_gemma":0.0001044282,"threshold_uncertainty_score":0.002868235},"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":"W2171385037","doi":"10.1016/j.placenta.2005.12.001","title":"Characterization of the Placenta Specific Bovine Mammalian Achaete Scute-like Homologue 2 (Mash2) Gene","year":2006,"lang":"en","type":"article","venue":"Placenta","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":23,"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; Cegep de Saint Hyacinthe","funders":"Institute of Human Development, Child and Youth Health; Natural Sciences and Engineering Research Council of Canada","keywords":"Biology; Trophoblast; Placenta; Gene; Genomic imprinting; Messenger RNA; Gene expression; Molecular biology; Genetics; DNA methylation; Fetus","score_opus":0.007069917725459457,"score_gpt":0.19461328874034348,"score_spread":0.18754337101488402,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2171385037","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9887017,0.0024477297,0.0053666416,0.00025225885,0.00003806117,0.000023752382,0.0009151881,0.000047882986,0.0022067102],"genre_scores_gemma":[0.9886009,0.00094755314,0.003097802,0.00012097778,0.000022958171,0.000018330122,0.0029461775,0.00002628926,0.0042189867],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9999379,0.000008133372,0.000004829642,0.000019296142,0.00001686436,0.000012964161],"domain_scores_gemma":[0.99980694,0.00006732842,0.000036258112,0.000025265335,0.000020172887,0.00004414445],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00008995504,0.00019105403,0.00016086425,0.00036566824,0.00017363303,0.00028717233,0.00024550382,0.00032411463,0.0013029719],"category_scores_gemma":[0.00027338704,0.00016310008,0.0001955559,0.00019676825,0.00023933474,0.0001820353,0.0001887726,0.00050769874,0.0005098542],"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":[0.00006349236,0.000010492123,0.0006858742,0.000023463494,0.000005655403,0.00042867934,0.00003183023,0.000043246284,0.9975464,0.00019766582,0.000032904274,0.00093030534],"study_design_scores_gemma":[0.0000797302,0.00035475087,0.09359495,0.000030058758,0.000089355686,0.0099644605,0.00034074503,0.002719575,0.86373836,0.0005890972,0.028475147,0.000023700057],"about_ca_topic_score_codex":0.0010217616,"about_ca_topic_score_gemma":0.0012019027,"teacher_disagreement_score":0.0013029719,"about_ca_system_score_codex":0.00024865955,"about_ca_system_score_gemma":0.00018366319,"threshold_uncertainty_score":0.004358828},"labels":[],"label_agreement":null},{"id":"W2172727295","doi":"10.1089/153623003769645866","title":"Growth Restricted <i>In Vitro</i> Culture Conditions Alter the Imprinted Gene Expression Patterns of Mouse Embryonic Stem Cells","year":2003,"lang":"en","type":"article","venue":"Cloning and Stem Cells","topic":"Genetic Syndromes and Imprinting","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":"Université de Montréal","funders":"","keywords":"Biology; Genomic imprinting; Reprogramming; Epigenetics; Embryonic stem cell; DNA methylation; Cell biology; Gene expression; Gene; Regulation of gene expression; Genetics","score_opus":0.0075259584323903814,"score_gpt":0.21312907612889587,"score_spread":0.2056031176965055,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2172727295","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9912662,0.0016665331,0.004022927,0.00007418974,0.000031399715,0.000015231798,0.001003531,0.000061043575,0.0018590591],"genre_scores_gemma":[0.9881605,0.001872828,0.0042895814,0.0000770764,0.000016431073,0.000053708332,0.0025322041,0.0000518144,0.002945945],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99988604,0.000022591505,0.000014915023,0.000028889795,0.000028256864,0.00001934799],"domain_scores_gemma":[0.9998692,0.00003929024,0.00003485324,0.00002503879,0.000012533915,0.000019084073],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00011491716,0.00032076277,0.00017542347,0.00018074093,0.000116557225,0.00027494336,0.00016797437,0.00014764954,0.0010065099],"category_scores_gemma":[0.00012575425,0.00013294682,0.00016237587,0.00014471369,0.00021696648,0.00014536701,0.00020992993,0.00041974394,0.00039080833],"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":[0.000021324111,0.000004998637,0.00030756087,0.00001007884,0.0000020471273,0.000018912773,0.0000107683045,0.000030431402,0.9992206,0.000033848853,0.000012365258,0.0003271213],"study_design_scores_gemma":[0.0000026236146,0.00008545114,0.007824854,0.0000041211965,0.000014121554,0.00011644707,0.00002526709,0.00020315954,0.9904929,0.00003326114,0.0011952592,0.0000025922695],"about_ca_topic_score_codex":0.0009900833,"about_ca_topic_score_gemma":0.0022441938,"teacher_disagreement_score":0.0010065099,"about_ca_system_score_codex":0.00019019195,"about_ca_system_score_gemma":0.00015822153,"threshold_uncertainty_score":0.003367126},"labels":[],"label_agreement":null},{"id":"W2173045156","doi":"10.1186/s13148-015-0143-8","title":"Imprinting disorders: a group of congenital disorders with overlapping patterns of molecular changes affecting imprinted loci","year":2015,"lang":"en","type":"review","venue":"Clinical Epigenetics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":214,"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; Assistance publique-Hôpitaux de Paris; Bundesministerium für Bildung und Forschung; Seconda Università degli Studi di Napoli; Institute of Genetics; Institut National de la Santé et de la Recherche Médicale; European Cooperation in Science and Technology; Instituto de Salud Carlos III; National Institute for Health and Care Research","keywords":"Genomic imprinting; Epigenetics; Human genetics; Imprinting (psychology); Biology; Genetics; DNA methylation; Gene; Molecular genetics; Disease; Bioinformatics; Computational biology; Medicine; Gene expression; Internal medicine","score_opus":0.037804355574652976,"score_gpt":0.34524692443060395,"score_spread":0.307442568855951,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2173045156","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":[0.00024305037,0.99731714,0.00033434475,0.00034960423,0.00014969573,0.000005302358,0.000046757435,0.000018345556,0.0015356481],"genre_scores_gemma":[0.0017961594,0.99655175,0.00037498045,0.00018792012,0.00013831751,0.000007142244,0.00010062697,0.000003097177,0.0008400445],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.99983144,0.000026317826,0.000027527054,0.00002993855,0.00006543997,0.00001928706],"domain_scores_gemma":[0.99970776,0.00013122147,0.000054323515,0.00001005183,0.00005433035,0.00004221466],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0003927046,0.0007764113,0.0010753225,0.0031254054,0.00031899824,0.00084404816,0.0008485556,0.000847697,0.0037165303],"category_scores_gemma":[0.00073294603,0.00014993917,0.00035867302,0.0026533685,0.00065562915,0.00090459286,0.0008197192,0.0012486664,0.0020801786],"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":[0.00004019804,0.000026908374,0.00059896236,0.007947797,0.00008422773,0.00091072236,0.000099073455,0.00023054388,0.0017192569,0.005016233,0.023934284,0.95939165],"study_design_scores_gemma":[0.000008498557,0.000025628153,0.001123829,0.0016138498,0.000090958354,0.007522971,0.000068936235,0.0000397448,0.00048869196,0.002267325,0.9867338,0.00001581913],"about_ca_topic_score_codex":0.0010570412,"about_ca_topic_score_gemma":0.0020246608,"teacher_disagreement_score":0.0037165303,"about_ca_system_score_codex":0.0006387828,"about_ca_system_score_gemma":0.0011588108,"threshold_uncertainty_score":0.012433052},"labels":[],"label_agreement":null},{"id":"W2174847659","doi":"10.1002/ajmg.a.37402","title":"Severe connective tissue laxity including aortic dilatation in Sotos syndrome","year":2015,"lang":"en","type":"article","venue":"American Journal of Medical Genetics Part A","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":10,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Children's Hospital of Eastern Ontario; University of Ottawa","funders":"Canadian Institutes of Health Research; McGill University","keywords":"Boycott; Medicine; Library science; Family medicine; Sociology; Political science; Law; Politics","score_opus":0.027509324616941874,"score_gpt":0.3173268875463814,"score_spread":0.2898175629294395,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2174847659","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99401724,0.0006139572,0.0006210616,0.00045717414,0.00007481541,0.000020341931,0.0001393538,0.000050527142,0.004005634],"genre_scores_gemma":[0.99862134,0.00033106157,0.0004705567,0.00007214212,0.00012440872,0.0000065402637,0.000048755872,0.000008455613,0.00031683253],"study_design_codex":"case_report","study_design_gemma":"case_report","domain_scores_codex":[0.9997377,0.000048056114,0.00004495979,0.00005122508,0.00006918207,0.00004891942],"domain_scores_gemma":[0.99904686,0.00038169534,0.00026355236,0.000038255665,0.00003745139,0.00023227268],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00020097294,0.0012299101,0.0005143015,0.0019253963,0.000644808,0.00042996832,0.00047984696,0.0012051625,0.0021975616],"category_scores_gemma":[0.0014659453,0.00040097345,0.0004261185,0.00093972357,0.0012846219,0.00047687598,0.0006452325,0.00058374344,0.0002114313],"study_design_candidate":"case_report","study_design_consensus":"case_report","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00038829973,0.00004683027,0.060916785,0.00012320308,0.00006214105,0.887133,0.0004588866,0.00039558837,0.04387484,0.0017485615,0.0004997924,0.0043520723],"study_design_scores_gemma":[0.00007293445,0.00023356768,0.12511417,0.000034071465,0.00014170056,0.86223644,0.00035823922,0.00088585704,0.0072695673,0.002357496,0.0012546008,0.000041369483],"about_ca_topic_score_codex":0.00063198264,"about_ca_topic_score_gemma":0.0006563156,"teacher_disagreement_score":0.0021975616,"about_ca_system_score_codex":0.00026037378,"about_ca_system_score_gemma":0.00038291526,"threshold_uncertainty_score":0.0073515773},"labels":[],"label_agreement":null},{"id":"W2180090034","doi":"10.1155/2015/278287","title":"Three Siblings with Prader-Willi Syndrome: Brief Review of Sleep and Prader-Willi Syndrome","year":2015,"lang":"en","type":"article","venue":"Case Reports in Neurological Medicine","topic":"Genetic Syndromes and Imprinting","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":"Toronto Western Hospital; University of Toronto; University Health Network","funders":"","keywords":"Medicine; Sleep (system call); Pediatrics; Psychiatry","score_opus":0.02798860704608892,"score_gpt":0.26900204877914535,"score_spread":0.24101344173305644,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2180090034","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":[0.12617958,0.83693755,0.006577801,0.007777674,0.0046499292,0.00020769489,0.0002658838,0.00025437315,0.017149553],"genre_scores_gemma":[0.25674757,0.71982026,0.003498231,0.0060501397,0.008566327,0.000114826245,0.00041972302,0.000051465257,0.004731475],"study_design_codex":"case_report","study_design_gemma":"case_report","domain_scores_codex":[0.99947864,0.00010369666,0.00016919097,0.00010828366,0.00008737382,0.000052904204],"domain_scores_gemma":[0.9994999,0.00022518769,0.00013241521,0.000018406638,0.000044817007,0.00007934491],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00031249813,0.0011741477,0.0010591556,0.002459041,0.0006237039,0.0006975832,0.0008849023,0.0021048198,0.0016232282],"category_scores_gemma":[0.0011940764,0.0004605473,0.00053035055,0.0015322624,0.00078016816,0.001157365,0.00083809835,0.0013538458,0.0009184977],"study_design_candidate":"case_report","study_design_consensus":"case_report","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.000058955833,0.00012895325,0.018529644,0.0023473206,0.00012765283,0.8610202,0.001201875,0.00024604367,0.0028144366,0.0011424468,0.015316251,0.09706622],"study_design_scores_gemma":[0.0000060541565,0.00006841465,0.0070974533,0.0003795853,0.000060818038,0.95950514,0.0003283056,0.00006779206,0.00029569044,0.00045824557,0.03170427,0.00002823946],"about_ca_topic_score_codex":0.00091758225,"about_ca_topic_score_gemma":0.0012784572,"teacher_disagreement_score":0.002459041,"about_ca_system_score_codex":0.00038847383,"about_ca_system_score_gemma":0.00048149066,"threshold_uncertainty_score":0.005430281},"labels":[],"label_agreement":null},{"id":"W2206303315","doi":"10.1210/jc.2015-3895","title":"Resting Energy Expenditure Is Decreased in Pseudohypoparathyroidism Type 1A","year":2015,"lang":"en","type":"article","venue":"The Journal of Clinical Endocrinology & Metabolism","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":47,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":true,"ca_institutions":"Hospital for Sick Children; University of Toronto; Université de Montréal; SickKids Foundation; Centre Hospitalier Universitaire Sainte-Justine","funders":"National Institute of Diabetes and Digestive and Kidney Diseases; National Institutes of Health; National Center for Advancing Translational Sciences; Johns Hopkins University","keywords":"Resting energy expenditure; GNAS complex locus; Medicine; Endocrine system; Endocrinology; Internal medicine; Pseudohypoparathyroidism; Body mass index; Neurocognitive; Obesity; Hormone; Cohort; Energy expenditure; Pediatrics; Parathyroid hormone; Biology; Psychiatry","score_opus":0.06503032546723593,"score_gpt":0.3617859862144264,"score_spread":0.2967556607471905,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2206303315","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9996445,0.000094485964,0.000055523404,0.000013908532,0.0000018661589,0.0000022834845,0.00007413736,0.0000017307573,0.000111536254],"genre_scores_gemma":[0.9996561,0.000055638164,0.000083368555,0.000010368415,0.000003365143,0.0000037752782,0.00009979489,0.0000014715838,0.00008621608],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9998791,0.000027962247,0.000011278187,0.000027780998,0.00003533475,0.000018493396],"domain_scores_gemma":[0.9995659,0.00007718433,0.00023229829,0.000017193599,0.000031740496,0.00007569463],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0002532766,0.0003072582,0.00021877665,0.00044870703,0.00020687684,0.00027313305,0.0002284753,0.00029136645,0.0012019383],"category_scores_gemma":[0.0012007367,0.00013513662,0.0001664157,0.00040488172,0.0002933496,0.0001377434,0.00026020777,0.00032851283,0.000110982015],"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":[0.0005221888,0.000046436722,0.988938,0.000023404718,0.000046503865,0.00071014964,0.00016166497,0.00005094345,0.006924541,0.000021378104,0.000068977904,0.0024859011],"study_design_scores_gemma":[0.0000043744135,0.000113322916,0.9980782,0.0000021175445,0.000012135978,0.0013073931,0.000051941926,0.000054563778,0.0003045103,0.000010573323,0.00005942174,0.0000014149973],"about_ca_topic_score_codex":0.0029778967,"about_ca_topic_score_gemma":0.0033348447,"teacher_disagreement_score":0.0029778967,"about_ca_system_score_codex":0.00022770675,"about_ca_system_score_gemma":0.00013682886,"threshold_uncertainty_score":0.0059211254},"labels":[],"label_agreement":null},{"id":"W2219501799","doi":"10.1016/j.appet.2015.12.021","title":"A review of chemosensory perceptions, food preferences and food-related behaviours in subjects with Prader–Willi Syndrome","year":2015,"lang":"en","type":"review","venue":"Appetite","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","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":"Agriculture Food and Rural Development; University of Alberta","funders":"Canadian Institutes of Health Research; University of Alberta","keywords":"Perception; Food choice; Dysfunctional family; Psychology; Preference; Obesity; Food preference; Developmental psychology; Medicine; Clinical psychology; Neuroscience; Biology; Food science; Endocrinology","score_opus":0.031317537572964606,"score_gpt":0.2854373369697193,"score_spread":0.25411979939675466,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2219501799","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":[0.00016325268,0.99919134,0.00010408271,0.00014538686,0.0001273056,0.0000028421284,0.000033826207,0.0000036702681,0.00022836057],"genre_scores_gemma":[0.000583384,0.99863666,0.00019304686,0.00014221831,0.00018955489,0.000004339439,0.000043252778,0.0000010535508,0.00020658728],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.9997687,0.00003784819,0.000063774634,0.000049908376,0.00006567274,0.000014202387],"domain_scores_gemma":[0.9995851,0.00024670013,0.00005626039,0.000008149987,0.00007646416,0.000027316577],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0005858098,0.00085558306,0.0018890774,0.0023659798,0.00018600182,0.00072492764,0.0007835295,0.00091971003,0.0021444673],"category_scores_gemma":[0.0011503235,0.00025461116,0.0006646877,0.0019172081,0.0003705789,0.0008972265,0.00067404535,0.00102065,0.0006372328],"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":[0.00013769488,0.000060054645,0.0010104079,0.028384674,0.0002920705,0.00057300524,0.00007665629,0.00022238506,0.0014221104,0.0008513484,0.020213671,0.94675595],"study_design_scores_gemma":[0.00008705702,0.00027646488,0.0123314895,0.016374607,0.0011759134,0.00987225,0.00023607252,0.00022301989,0.0008689979,0.002013691,0.9564318,0.00010854484],"about_ca_topic_score_codex":0.0016681238,"about_ca_topic_score_gemma":0.0026481824,"teacher_disagreement_score":0.0023659798,"about_ca_system_score_codex":0.00033479495,"about_ca_system_score_gemma":0.00080874306,"threshold_uncertainty_score":0.007173896},"labels":[],"label_agreement":null},{"id":"W2232856929","doi":"10.1101/gr.196139.115","title":"Pervasive polymorphic imprinted methylation in the human placenta","year":2016,"lang":"en","type":"article","venue":"Genome Research","topic":"Genetic Syndromes and Imprinting","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":"Child and Family Research Institute; University of British Columbia","funders":"Medical Research Council; Canadian Institutes of Health Research; Child and Family Research Institute","keywords":"Differentially methylated regions; Genomic imprinting; Biology; DNA methylation; Imprinting (psychology); Methylation; Germline; Epigenetics; Genetics; Bisulfite sequencing; Placenta; Gene; Gene expression; Fetus; Pregnancy","score_opus":0.06737292024968491,"score_gpt":0.3631432697790212,"score_spread":0.29577034952933634,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2232856929","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.97817546,0.009096596,0.008524323,0.00012591164,0.000012209298,0.000019709254,0.0016102295,0.00016701307,0.00226852],"genre_scores_gemma":[0.9947478,0.0017810629,0.0024354241,0.000037218037,0.000004849416,0.000008035481,0.00051477866,0.000017251832,0.00045347877],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.99984336,0.00002868092,0.000008167439,0.00006241619,0.000041706222,0.0000156288],"domain_scores_gemma":[0.9998908,0.000023347591,0.00004350156,0.00001624332,0.000014500969,0.000011553014],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00018001976,0.00010083873,0.00016630911,0.00044772087,0.000112830516,0.00032591244,0.00013168927,0.00011912997,0.0006007098],"category_scores_gemma":[0.00035360863,0.00015249735,0.00012905386,0.0005171874,0.00019758947,0.00009076154,0.00025489897,0.00015261618,0.00014524149],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00048989546,0.000012171242,0.11969438,0.00021313652,0.00017538854,0.0010399602,0.00055450475,0.00064915774,0.8336906,0.00085202674,0.0004901324,0.04213869],"study_design_scores_gemma":[0.000024738612,0.00018189907,0.838213,0.00003605617,0.00015923317,0.005546971,0.00023631215,0.001891103,0.14029278,0.0013705225,0.012024768,0.000022565571],"about_ca_topic_score_codex":0.0020993743,"about_ca_topic_score_gemma":0.0023712271,"teacher_disagreement_score":0.0020993743,"about_ca_system_score_codex":0.0001960353,"about_ca_system_score_gemma":0.00019629922,"threshold_uncertainty_score":0.0041743517},"labels":[],"label_agreement":null},{"id":"W2254272094","doi":"10.1038/srep10596","title":"Assisted reproduction causes placental maldevelopment and dysfunction linked to reduced fetal weight in mice","year":2015,"lang":"en","type":"article","venue":"Scientific Reports","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":105,"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":"Offspring; Maldevelopment; Genomic imprinting; Placenta; Fetus; Placentation; Biology; Andrology; In utero; Pregnancy; Low birth weight; Embryo; Imprinting (psychology); Birth weight; Epigenetics; Downregulation and upregulation; Endocrinology; Cell biology; Medicine; Genetics; Gene expression; DNA methylation; Gene; Anatomy","score_opus":0.02024845168967122,"score_gpt":0.24717084596980682,"score_spread":0.2269223942801356,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2254272094","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9784535,0.0035729376,0.008991831,0.00048450095,0.00011544731,0.000102966704,0.0038085082,0.0007084007,0.0037617676],"genre_scores_gemma":[0.97628003,0.0039672838,0.0065284343,0.00026419177,0.00003446382,0.00026289886,0.002254318,0.00020967245,0.010198773],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99954337,0.00008259079,0.000049041908,0.00013603889,0.00011936845,0.00006948392],"domain_scores_gemma":[0.99948287,0.00008193537,0.00022861919,0.00007824632,0.000017707689,0.000110570625],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00036307916,0.00070035533,0.00034023647,0.0016182938,0.000306378,0.0004991067,0.000600123,0.0007333429,0.003231466],"category_scores_gemma":[0.0003005742,0.0006018494,0.0007748145,0.0004779024,0.00070089684,0.00027458055,0.00052172854,0.0012886825,0.0005383116],"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":[0.0005274053,0.00013132006,0.00078320026,0.00009174615,0.00005041005,0.0007183826,0.000080885424,0.00025818005,0.99314284,0.0009442339,0.0002046252,0.00306665],"study_design_scores_gemma":[0.00017890333,0.0012426017,0.018854791,0.000068577676,0.0001697406,0.0029619525,0.00012807587,0.0027785697,0.9629673,0.00083874975,0.009776448,0.00003436618],"about_ca_topic_score_codex":0.00073190924,"about_ca_topic_score_gemma":0.0010336073,"teacher_disagreement_score":0.003231466,"about_ca_system_score_codex":0.0004890318,"about_ca_system_score_gemma":0.00031490385,"threshold_uncertainty_score":0.010810316},"labels":[],"label_agreement":null},{"id":"W2256023856","doi":"10.1172/jci80937","title":"TGF-β/β2-spectrin/CTCF-regulated tumor suppression in human stem cell disorder Beckwith-Wiedemann syndrome","year":2016,"lang":"en","type":"article","venue":"Journal of Clinical Investigation","topic":"Genetic Syndromes and Imprinting","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":"Hospital for Sick Children","funders":"National Institute of Diabetes and Digestive and Kidney Diseases; National Heart, Lung, and Blood Institute; National Institute on Alcohol Abuse and Alcoholism; University of Texas MD Anderson Cancer Center; Directorate for Biological Sciences; George Washington University; American Cancer Society; U.S. Department of Veterans Affairs; National Cancer Institute; National Institutes of Health","keywords":"Beckwith–Wiedemann syndrome; CTCF; Medicine; Spectrin; Biology; Cancer research; Immunology; Genetics; Cell; Gene; Transcription factor","score_opus":0.030103862795979115,"score_gpt":0.31492420656648573,"score_spread":0.28482034377050663,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2256023856","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.995742,0.0007775666,0.0020076355,0.00006885709,0.000019245434,0.000016007361,0.00034026793,0.00012380489,0.00090448116],"genre_scores_gemma":[0.9972199,0.0004582187,0.0010630207,0.00003137137,0.00000537423,0.0000120528275,0.00030930765,0.000012950518,0.00088783464],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.999938,0.000009332982,0.0000075313847,0.000018068473,0.000017406965,0.000009645299],"domain_scores_gemma":[0.9999304,0.0000093287645,0.000027378888,0.000004705978,0.000003319672,0.000024847328],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00006276458,0.00049540604,0.00016558582,0.0004443954,0.00014882273,0.00013982128,0.00009598692,0.00023809818,0.0014485401],"category_scores_gemma":[0.000108632026,0.00013691671,0.00021793348,0.00019405062,0.00026282127,0.0000664271,0.00019063022,0.0002854488,0.0002447209],"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":[0.00008449672,0.000016988024,0.0029650931,0.00003023773,0.000017184895,0.0025651762,0.000027106582,0.00009665698,0.99156696,0.00024317531,0.000098552555,0.002288377],"study_design_scores_gemma":[0.00011787443,0.00047449965,0.120164976,0.000041608473,0.00015171214,0.055033296,0.00013850999,0.0031461597,0.811816,0.0005836685,0.00830307,0.000028594193],"about_ca_topic_score_codex":0.0006645816,"about_ca_topic_score_gemma":0.0012427114,"teacher_disagreement_score":0.0014485401,"about_ca_system_score_codex":0.00013438016,"about_ca_system_score_gemma":0.00016419892,"threshold_uncertainty_score":0.0048458576},"labels":[],"label_agreement":null},{"id":"W2267339756","doi":"","title":"발달장애 아동의 기능적응을 위한 감각치료에 관한 연구","year":2013,"lang":"ko","type":"article","venue":"한국유아교육·보육복지연구","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":0,"is_retracted":false,"has_abstract":true,"route_ca_aff":false,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":true,"ca_institutions":"","funders":"","keywords":"Focus (optics); Occupational therapy; Psychology; Medicine; Physical medicine and rehabilitation; Physical therapy","score_opus":0.007234114929904836,"score_gpt":0.22078330178963093,"score_spread":0.2135491868597261,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2267339756","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.91157645,0.0028694924,0.00167554,0.019796371,0.0016100423,0.00026278634,0.0013736951,0.00007162451,0.060763985],"genre_scores_gemma":[0.953932,0.0023785287,0.002165857,0.0081675695,0.00038742603,0.00044490982,0.0011137696,0.000033263736,0.031376667],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99942005,0.00014459345,0.00007222922,0.00007732277,0.00016969183,0.000116234296],"domain_scores_gemma":[0.9992092,0.0002769296,0.0001305203,0.000041822957,0.00021548342,0.00012605613],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00071299105,0.00025339593,0.0002757304,0.00074734323,0.0016088967,0.00072023616,0.0003024643,0.00037970333,0.011494798],"category_scores_gemma":[0.0037416115,0.00009524665,0.00033412184,0.0006009827,0.00062967633,0.00073682476,0.00046414204,0.0008680795,0.0015040089],"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":[0.0002680396,0.0005730975,0.8081513,0.00039604396,0.000077754274,0.007612366,0.01616087,0.0001286641,0.0032668924,0.0113305105,0.03874786,0.11328657],"study_design_scores_gemma":[0.00009789501,0.0007040527,0.63785523,0.0008289512,0.00022586792,0.041120347,0.050536998,0.0002474306,0.004531358,0.008436133,0.2553319,0.00008376695],"about_ca_topic_score_codex":0.010233706,"about_ca_topic_score_gemma":0.030606821,"teacher_disagreement_score":0.011494798,"about_ca_system_score_codex":0.0009853565,"about_ca_system_score_gemma":0.001534088,"threshold_uncertainty_score":0.038453877},"labels":[],"label_agreement":null},{"id":"W2267376195","doi":"10.1038/ncomms10207","title":"NSD1 mutations generate a genome-wide DNA methylation signature","year":2015,"lang":"en","type":"article","venue":"Nature Communications","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":211,"is_retracted":false,"has_abstract":true,"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 of New Brunswick; University of Alberta; Child and Family Research Institute; Canada Research Chairs; Hospital for Sick Children","funders":"Canadian Institutes of Health Research; Rare Disease Foundation","keywords":"Epigenetics; Genetics; Methyltransferase; Biology; Genome; Gene; Histone; DNA methylation; Phenotype; Methylation; dNaM; Computational biology; Gene expression","score_opus":0.02523140765637531,"score_gpt":0.2936934390081372,"score_spread":0.2684620313517619,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2267376195","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9971727,0.00016006737,0.0013199762,0.00003572291,0.0000058136243,0.000015111844,0.0006182165,0.000060945007,0.0006113399],"genre_scores_gemma":[0.9982399,0.00008451107,0.00088353234,0.000032455293,0.0000027527578,0.000009366363,0.00051484874,0.00000868941,0.00022393427],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9998185,0.000027177915,0.000018711396,0.000060400667,0.00005644068,0.000018763469],"domain_scores_gemma":[0.9998018,0.000058676287,0.00007025217,0.000023826584,0.000017137798,0.000028338356],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00016351724,0.00029226983,0.00019229643,0.00049073156,0.00011292566,0.00017710903,0.00014354209,0.0002683439,0.0011521834],"category_scores_gemma":[0.0005806233,0.000119839904,0.00016364639,0.00023465676,0.00020437727,0.00007844814,0.0003593716,0.00015785565,0.00017768447],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00051204476,0.000029506746,0.1440799,0.000056227702,0.00007531356,0.00095465797,0.00014717932,0.0005242156,0.8369951,0.00041582683,0.0003880507,0.015821856],"study_design_scores_gemma":[0.00005405542,0.00037117486,0.72645533,0.0000181862,0.00010084157,0.014664951,0.0001382675,0.0037238728,0.24988107,0.000772839,0.0037940005,0.00002532046],"about_ca_topic_score_codex":0.0006085615,"about_ca_topic_score_gemma":0.0011673466,"teacher_disagreement_score":0.0011521834,"about_ca_system_score_codex":0.00015939419,"about_ca_system_score_gemma":0.0000907721,"threshold_uncertainty_score":0.0038544536},"labels":[],"label_agreement":null},{"id":"W2274471732","doi":"10.3109/14767058.2016.1138465","title":"Epigenetic Dysregulation of Insulin-like Growth Factor (IGF)-related Genes and Adverse Pregnancy Outcomes: A Systematic Review","year":2016,"lang":"en","type":"review","venue":"The Journal of Maternal-Fetal & Neonatal Medicine","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":11,"is_retracted":false,"has_abstract":true,"route_ca_aff":false,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":true,"ca_institutions":"","funders":"","keywords":"Epigenetics; Low birth weight; Small for gestational age; Observational study; Medicine; Birth weight; Bioinformatics; Genomic imprinting; Pregnancy; DNA methylation; Oncology; Genetics; Internal medicine; Biology; Gene","score_opus":0.01592236954165377,"score_gpt":0.2814813707652216,"score_spread":0.26555900122356785,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2274471732","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":[0.0004242926,0.9989405,0.00007261128,0.00015444146,0.00006350886,0.00007454532,0.00013111414,0.0000035971505,0.00013543092],"genre_scores_gemma":[0.0057978923,0.99336,0.00023361517,0.00022391751,0.000050907474,0.0001557084,0.00009891719,0.0000020332309,0.00007701666],"study_design_codex":"systematic_review","study_design_gemma":"systematic_review","domain_scores_codex":[0.9970151,0.000960437,0.0010519931,0.00029951165,0.0005471567,0.00012572682],"domain_scores_gemma":[0.9876385,0.008740508,0.0021886204,0.0001727242,0.0010974879,0.00016214969],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0048143105,0.0013462732,0.0059366664,0.00672699,0.00051667716,0.0017362937,0.0018177737,0.0016267635,0.004045679],"category_scores_gemma":[0.022232559,0.0007430235,0.004134135,0.008260606,0.00067555084,0.0017415406,0.0011529647,0.00074380107,0.00030612954],"study_design_candidate":"systematic_review","study_design_consensus":"systematic_review","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00013438863,0.000011435566,0.0008545785,0.93859476,0.005283579,0.0001555177,0.00015962165,0.00009832494,0.00017730115,0.00025620588,0.0021218287,0.052152418],"study_design_scores_gemma":[0.00019421613,0.00019558823,0.00695666,0.8834185,0.072146654,0.0009235824,0.00027954482,0.000107024185,0.00029932748,0.00048990577,0.034939334,0.000049738414],"about_ca_topic_score_codex":0.006253642,"about_ca_topic_score_gemma":0.016601996,"teacher_disagreement_score":0.00672699,"about_ca_system_score_codex":0.0023030315,"about_ca_system_score_gemma":0.009759906,"threshold_uncertainty_score":0.02546084},"labels":[],"label_agreement":null},{"id":"W2283197660","doi":"10.71781/3667","title":"Study of imprinted genes in bovine embryos produced by assisted reproductive technologies","year":2008,"lang":"en","type":"dissertation","venue":"Open MIND","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":0,"is_retracted":false,"has_abstract":true,"route_ca_aff":false,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":true,"ca_institutions":"","funders":"Natural Sciences and Engineering Research Council of Canada; Canadian Institutes of Health Research; Conselho Nacional de Desenvolvimento Científico e Tecnológico","keywords":"Embryo; Genomic imprinting; Andrology; Biology; Gene; Genetics; Biotechnology; Medicine; Gene expression","score_opus":0.0258992838831357,"score_gpt":0.3096075164327498,"score_spread":0.2837082325496141,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2283197660","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.971046,0.011714858,0.0038451967,0.00021030511,0.000085617045,0.00004588917,0.001434867,0.00003780699,0.011579425],"genre_scores_gemma":[0.96463114,0.005491853,0.002611544,0.00010413172,0.000024186644,0.000042429376,0.0019997486,0.00003731539,0.025057625],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9998938,0.000020544294,0.000005407503,0.00002611131,0.000033181754,0.000021033215],"domain_scores_gemma":[0.9998104,0.00009277489,0.000026312553,0.000013669819,0.000029340788,0.000027579948],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00022444504,0.00010990905,0.00016979873,0.0005156912,0.00027802752,0.00031236824,0.00025162662,0.00029911287,0.0026446406],"category_scores_gemma":[0.000330921,0.00010925669,0.00018082022,0.00028138544,0.0002578677,0.000113033064,0.00012872167,0.00035253455,0.0004897647],"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":[0.00026199757,0.000030079495,0.004230105,0.00008067204,0.000019400824,0.00045204328,0.00019955463,0.000063480984,0.98484206,0.00033722972,0.00015774377,0.009325622],"study_design_scores_gemma":[0.000057198347,0.0007376299,0.45890874,0.00007499153,0.00008801679,0.0014388636,0.00054150925,0.00042421103,0.51461715,0.0003024379,0.022794496,0.000014827869],"about_ca_topic_score_codex":0.004270576,"about_ca_topic_score_gemma":0.004770162,"teacher_disagreement_score":0.004270576,"about_ca_system_score_codex":0.00031079593,"about_ca_system_score_gemma":0.0001955186,"threshold_uncertainty_score":0.008847177},"labels":[],"label_agreement":null},{"id":"W2314857307","doi":"10.1097/00001577-200001220-00006","title":"Prader-Willi Syndrome","year":2000,"lang":"en","type":"article","venue":"Pediatric Physical Therapy","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":4,"is_retracted":false,"has_abstract":true,"route_ca_aff":false,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":true,"ca_institutions":"","funders":"","keywords":"Intervention (counseling); Medicine; Family medicine; Association (psychology); MEDLINE; Pediatrics; Physical therapy; Psychology; Nursing; Political science","score_opus":0.01033319299372057,"score_gpt":0.24615006921483973,"score_spread":0.23581687622111916,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2314857307","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":[0.7803087,0.035372883,0.02610382,0.022297727,0.0037559457,0.0009554461,0.005248826,0.0018494579,0.12410716],"genre_scores_gemma":[0.9463469,0.011244256,0.012314506,0.0024033117,0.0011237337,0.0002435193,0.00093188864,0.0001205815,0.025271328],"study_design_codex":"case_report","study_design_gemma":"not_applicable","domain_scores_codex":[0.9993529,0.000088349225,0.000034184504,0.00022863502,0.00019947265,0.00009649538],"domain_scores_gemma":[0.9990085,0.00034822788,0.00032030337,0.000069199414,0.000085743086,0.00016800333],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00025073264,0.0020968504,0.00091785245,0.0020874399,0.0011995987,0.0006208298,0.0011097668,0.0019945484,0.0082357],"category_scores_gemma":[0.0037244358,0.00038316904,0.00044068883,0.0010700607,0.0014322121,0.0010094128,0.001350106,0.002640442,0.0018362924],"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":[0.00014912864,0.00008471864,0.012984525,0.00020563055,0.00014191084,0.9264821,0.00045831714,0.0005891237,0.012239263,0.0136483265,0.00852929,0.024487639],"study_design_scores_gemma":[0.00003180471,0.000055885477,0.011856608,0.0000789166,0.00006384854,0.9689947,0.000080912505,0.00029877148,0.0021945292,0.003064599,0.013249183,0.000030310199],"about_ca_topic_score_codex":0.0019849346,"about_ca_topic_score_gemma":0.0017135695,"teacher_disagreement_score":0.0082357,"about_ca_system_score_codex":0.00048037095,"about_ca_system_score_gemma":0.00085655414,"threshold_uncertainty_score":0.027551115},"labels":[],"label_agreement":null},{"id":"W2315270862","doi":"10.15331/jdsm.3900","title":"Macroglossia and Down Syndrome: Don't Be Fooled","year":2014,"lang":"en","type":"article","venue":"Journal of Dental Sleep Medicine","topic":"Genetic Syndromes and Imprinting","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":"University of Alberta","funders":"","keywords":"Macroglossia; Medicine; Philosophy; Linguistics; Tongue","score_opus":0.005697273049798441,"score_gpt":0.23590983015897382,"score_spread":0.23021255710917538,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2315270862","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":[0.021877479,0.640162,0.0008913538,0.28133738,0.042752307,0.00005842063,0.00059798476,0.00006506238,0.01225804],"genre_scores_gemma":[0.20194118,0.41430116,0.0028393336,0.24329117,0.11922553,0.00024827028,0.0007948696,0.000053432675,0.017305097],"study_design_codex":"design_other","study_design_gemma":"case_report","domain_scores_codex":[0.99942434,0.0002066566,0.00009740833,0.000083994615,0.00014254266,0.000045115074],"domain_scores_gemma":[0.9979232,0.0012672499,0.0002419327,0.00009272773,0.0002580346,0.000216828],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.001576323,0.0003316139,0.0011356998,0.00045734885,0.0004742226,0.00085808383,0.000644581,0.0022492646,0.0042080646],"category_scores_gemma":[0.007156074,0.000147985,0.00033286185,0.0003497339,0.0009168648,0.0017538103,0.00060868886,0.0018384028,0.00095823524],"study_design_candidate":"case_report","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00187002,0.00023515655,0.024170998,0.005787372,0.000767084,0.0058628535,0.0009097563,0.00014881023,0.0018479587,0.006757947,0.2710001,0.6806419],"study_design_scores_gemma":[0.000765183,0.0016512867,0.044491258,0.0076686796,0.0010346309,0.024329523,0.0029737083,0.00023309483,0.00091260095,0.025773976,0.8900515,0.00011452848],"about_ca_topic_score_codex":0.0017875138,"about_ca_topic_score_gemma":0.004136311,"teacher_disagreement_score":0.0042080646,"about_ca_system_score_codex":0.00033326703,"about_ca_system_score_gemma":0.0008661164,"threshold_uncertainty_score":0.014077365},"labels":[],"label_agreement":null},{"id":"W2315847851","doi":"10.1016/s1499-2671(08)24294-2","title":"Pseudohypoparathyroidism type 1a and the GNAS p.R231H mutation: somatic and gonadal mosaicism in a mother with 2 affected sons","year":2008,"lang":"en","type":"article","venue":"Canadian Journal of Diabetes","topic":"Genetic Syndromes and Imprinting","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":true,"route_about_ca":false,"ca_institutions":"University of British Columbia","funders":"","keywords":"GNAS complex locus; Pseudohypoparathyroidism; Medicine; Gs alpha subunit; Short stature; Endocrinology; Internal medicine; Brachydactyly; Mutation; Somatic cell; Adenylyl cyclase; Parathyroid hormone; Obesity; Receptor; Genetics; Gene; Biology","score_opus":0.005658972180609143,"score_gpt":0.18260078256213375,"score_spread":0.1769418103815246,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2315847851","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99491644,0.00043026824,0.00052384794,0.00092044816,0.000109326254,0.000053852076,0.00021718412,0.000036659745,0.002791966],"genre_scores_gemma":[0.9967805,0.00029465655,0.0007162275,0.00018661917,0.00011416258,0.000014282841,0.00007172107,0.000027595037,0.0017941096],"study_design_codex":"case_report","study_design_gemma":"case_report","domain_scores_codex":[0.99941826,0.000054106065,0.00006625763,0.00016006701,0.00015298426,0.00014838041],"domain_scores_gemma":[0.99881697,0.00039908325,0.00019892753,0.000052113595,0.00006881515,0.0004641261],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00035027543,0.0014520905,0.0008995463,0.0022791894,0.0016023307,0.0008941359,0.001384697,0.0025065362,0.002826591],"category_scores_gemma":[0.0024676907,0.00094239105,0.000980912,0.00090614986,0.0015434081,0.0005826168,0.0010187067,0.0015785799,0.00048439225],"study_design_candidate":"case_report","study_design_consensus":"case_report","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00006986706,0.00004562151,0.008152678,0.000011845078,0.000011461609,0.9873975,0.00034645124,0.000064782274,0.002605352,0.00013591988,0.00011368689,0.0010448415],"study_design_scores_gemma":[0.000022969198,0.00013468048,0.021279769,0.000009113151,0.000026594089,0.97634333,0.00024106467,0.0002891797,0.0011758419,0.00010091307,0.00035597096,0.000020563552],"about_ca_topic_score_codex":0.014800029,"about_ca_topic_score_gemma":0.013115284,"teacher_disagreement_score":0.014800029,"about_ca_system_score_codex":0.0013958978,"about_ca_system_score_gemma":0.00086456584,"threshold_uncertainty_score":0.029427767},"labels":[],"label_agreement":null},{"id":"W2318267505","doi":"10.1038/sj.mp.4001098","title":"Dopamine D4 receptor and tyrosine hydroxylase genes in bipolar disorder: evidence for a role of DRD4","year":2002,"lang":"en","type":"article","venue":"Molecular Psychiatry","topic":"Genetic Syndromes and Imprinting","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":"Health Sciences Centre; University of Manitoba; Centre for Addiction and Mental Health; University of Toronto","funders":"","keywords":"Genetics; Transmission disequilibrium test; Bipolar disorder; Allele; Biology; Linkage disequilibrium; Dopamine; Genomic imprinting; Gene; Haplotype; Endocrinology","score_opus":0.009990049899582775,"score_gpt":0.24030591042897598,"score_spread":0.2303158605293932,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2318267505","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9894777,0.00460707,0.00072202046,0.00069573737,0.000035020774,0.000006647179,0.00023008343,0.000021570282,0.0042041587],"genre_scores_gemma":[0.99650747,0.0016591769,0.0004957021,0.00009730724,0.000025982754,0.0000053818035,0.0001040156,0.0000063153025,0.0010986296],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9999155,0.000023574552,0.00000792396,0.000014233491,0.000020061609,0.000018790557],"domain_scores_gemma":[0.9998622,0.00004904183,0.000035098255,0.0000120053655,0.000013946271,0.000027762357],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00019144043,0.0002913867,0.00018414696,0.000718396,0.0002456417,0.0002512359,0.00030986546,0.00040250804,0.0022587357],"category_scores_gemma":[0.00042869,0.00016965582,0.00014491197,0.0003975561,0.0005114319,0.00014451526,0.0002120881,0.0002695696,0.00015827964],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0071982048,0.00018756563,0.27591875,0.00024824688,0.00040546127,0.032150794,0.00062493625,0.0013429369,0.6248032,0.008681886,0.0016070743,0.046830904],"study_design_scores_gemma":[0.00053411315,0.0005963684,0.8509637,0.00007030194,0.0007386347,0.061197538,0.0008605343,0.0019324363,0.064462446,0.008273004,0.010328471,0.000042325526],"about_ca_topic_score_codex":0.002815495,"about_ca_topic_score_gemma":0.0020289866,"teacher_disagreement_score":0.002815495,"about_ca_system_score_codex":0.00030230344,"about_ca_system_score_gemma":0.00025053168,"threshold_uncertainty_score":0.0075562596},"labels":[],"label_agreement":null},{"id":"W2322812678","doi":"10.12703/p7-20","title":"Sublingual thyroid ectopy: similarities and differences with Kallmann syndrome","year":2015,"lang":"en","type":"review","venue":"F1000Prime Reports","topic":"Genetic Syndromes and Imprinting","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":"Université de Montréal; Centre Hospitalier Universitaire Sainte-Justine; HEC Montréal","funders":"Canadian Institutes of Health Research; Centre hospitalier universitaire Sainte-Justine","keywords":"Thyroid; Ectopic thyroid; Medicine; Congenital hypothyroidism; Internal medicine; Endocrinology; Thyroid disease; Pathology","score_opus":0.031505076523798234,"score_gpt":0.2891671972331874,"score_spread":0.25766212070938915,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2322812678","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":[0.000268776,0.99812764,0.00016455853,0.00038785345,0.00016156433,0.000002764539,0.000015399315,0.00000948509,0.0008620363],"genre_scores_gemma":[0.0020915887,0.99646384,0.000275086,0.00028967002,0.00024911485,0.000004888519,0.000046487658,0.0000034459708,0.0005758318],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.9998136,0.00002558874,0.000042162155,0.000039511924,0.00005931522,0.000019737085],"domain_scores_gemma":[0.9997024,0.0001478414,0.000050934654,0.000009159878,0.0000509798,0.00003872314],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00039875822,0.0006128031,0.0012503994,0.0030055773,0.0002541685,0.0007604329,0.00082500675,0.0009975547,0.0023906368],"category_scores_gemma":[0.0009394282,0.00020249614,0.00046803127,0.0022562472,0.00061703566,0.0009827394,0.0006398473,0.0015859364,0.0009684173],"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":[0.000070443995,0.000036818165,0.0008730565,0.010987897,0.00012775724,0.0036530532,0.00014583381,0.00026724968,0.0015127902,0.0039163087,0.026430612,0.9519782],"study_design_scores_gemma":[0.00002906688,0.00006606143,0.003682914,0.0040944926,0.00024236989,0.053260844,0.00015962927,0.00009451085,0.0006443752,0.0035749394,0.93411386,0.000036792084],"about_ca_topic_score_codex":0.001079738,"about_ca_topic_score_gemma":0.0019044608,"teacher_disagreement_score":0.0030055773,"about_ca_system_score_codex":0.00057790993,"about_ca_system_score_gemma":0.00076845364,"threshold_uncertainty_score":0.007997453},"labels":[],"label_agreement":null},{"id":"W2323605318","doi":"10.2174/1573400510666140319234658","title":"Prader-Willi Syndrome: Genetics, Phenotype, and Management","year":2014,"lang":"en","type":"article","venue":"Current Psychiatry Reviews","topic":"Genetic Syndromes and Imprinting","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":"McMaster Children's Hospital; McMaster University","funders":"","keywords":"Hypotonia; Psychosis; Intellectual disability; Medicine; Failure to thrive; Autism; Neurodevelopmental disorder; Autism spectrum disorder; Psychiatry; Phenotype; Psychology; Genetics; Pediatrics; Biology; Gene","score_opus":0.019588437047842914,"score_gpt":0.28202949986877685,"score_spread":0.26244106282093393,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2323605318","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":[0.123190045,0.7632414,0.027542572,0.038217224,0.0010235689,0.0003255339,0.0008527676,0.0005205769,0.045086253],"genre_scores_gemma":[0.45918602,0.50043064,0.022380523,0.0055002365,0.0022567697,0.0002316807,0.0009767368,0.000055727323,0.008981647],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.9998436,0.000038818915,0.000023232305,0.000020265064,0.000056540794,0.00001750323],"domain_scores_gemma":[0.999902,0.0000322665,0.000019778325,0.0000041827275,0.000020560909,0.000021190006],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00032219896,0.00046332006,0.00054439745,0.00067423773,0.00027331433,0.00034173654,0.00043406244,0.000625849,0.0006543454],"category_scores_gemma":[0.00081364566,0.00011614539,0.00016455613,0.0003932615,0.00030250353,0.0004258523,0.00047118132,0.0012124706,0.00033911486],"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":[0.00019767856,0.0002213481,0.057769626,0.0017793404,0.000115867835,0.08534685,0.00069229194,0.0010499491,0.015022875,0.015369939,0.046141665,0.77629256],"study_design_scores_gemma":[0.00006710959,0.0002619984,0.09215275,0.0027428668,0.00016863419,0.74599403,0.0010493346,0.0014416655,0.0038830051,0.01789561,0.13426116,0.00008186532],"about_ca_topic_score_codex":0.0008695029,"about_ca_topic_score_gemma":0.0011239932,"teacher_disagreement_score":0.0008695029,"about_ca_system_score_codex":0.00042725352,"about_ca_system_score_gemma":0.00047117798,"threshold_uncertainty_score":0.0030999184},"labels":[],"label_agreement":null},{"id":"W2325566001","doi":"10.1139/gen-2013-0062","title":"Comparative analysis of the <i>IGF2</i> and <i>ZBED6</i> gene variants and haplotypes reveals significant effect of growth traits in cattle","year":2013,"lang":"en","type":"article","venue":"Genome","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":9,"is_retracted":false,"has_abstract":true,"route_ca_aff":false,"route_ca_fund":false,"route_ca_venue":true,"route_about_ca":false,"ca_institutions":"","funders":"","keywords":"Biology; Haplotype; Genetics; Linkage disequilibrium; Single-nucleotide polymorphism; Allele; Heterozygote advantage; Gene; Genotype","score_opus":0.007202621978442396,"score_gpt":0.2202007359054904,"score_spread":0.212998113927048,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2325566001","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99960583,0.00005723334,0.00016410182,0.000005482218,0.0000016349804,0.000001421058,0.00008119841,0.000001330918,0.000081764745],"genre_scores_gemma":[0.999549,0.0000247518,0.00015344204,0.000010331456,0.0000029286953,0.0000033070517,0.00014092764,0.0000022853096,0.00011307031],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99954957,0.00011284093,0.00003956136,0.00016743325,0.000065230575,0.00006540168],"domain_scores_gemma":[0.99969435,0.000100741854,0.00008914652,0.000016019987,0.000017383449,0.00008238849],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00041403482,0.0002502204,0.000314221,0.00068218296,0.00026735864,0.00025402074,0.00019401197,0.00023292878,0.0013484913],"category_scores_gemma":[0.00041109812,0.00013486668,0.00031849227,0.0005238905,0.00035411702,0.00009321026,0.00019763639,0.00026439232,0.00012302378],"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":[0.0022782204,0.00007598073,0.8034555,0.00006075172,0.00059069175,0.0011611999,0.0007223282,0.00033419777,0.18245392,0.00019117499,0.00011929167,0.008556813],"study_design_scores_gemma":[0.000020496134,0.0000873926,0.997721,0.0000052859114,0.00006806753,0.00047809735,0.00010067291,0.00038708697,0.00090210093,0.00003221802,0.00019268636,0.0000049820947],"about_ca_topic_score_codex":0.0022688985,"about_ca_topic_score_gemma":0.0031758074,"teacher_disagreement_score":0.0022688985,"about_ca_system_score_codex":0.00015837913,"about_ca_system_score_gemma":0.00010889567,"threshold_uncertainty_score":0.004511416},"labels":[],"label_agreement":null},{"id":"W2327465536","doi":"10.1017/s0317167100022599","title":"DIETARY TREATMENT OF EPILEPSY. PRACTICAL IMPLEMENTATION OF KETOGENIC THERAPY. 2012. Edited by Elizabeth Neal. Published by Wiley-Blackwell. 241 pages. C$80 approx.","year":2013,"lang":"en","type":"article","venue":"Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":2,"is_retracted":false,"has_abstract":true,"route_ca_aff":false,"route_ca_fund":false,"route_ca_venue":true,"route_about_ca":false,"ca_institutions":"","funders":"","keywords":"Ketogenic diet; Approx; Action (physics); Epilepsy; Gerontology; Psychology; Medicine; Neuroscience; Computer science; Physics; Computer security","score_opus":0.02968155150110296,"score_gpt":0.2838706410746815,"score_spread":0.25418908957357855,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2327465536","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":[0.0011981938,0.8493458,0.0066015525,0.016172182,0.016045166,0.00014076033,0.00095492357,0.0010327238,0.10850869],"genre_scores_gemma":[0.0061255917,0.7186087,0.012271202,0.0024750936,0.0047514886,0.00013822326,0.00070615445,0.0002702923,0.25465325],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.9998317,0.000035889763,0.000024362262,0.000019904313,0.00007446503,0.000013738397],"domain_scores_gemma":[0.99973935,0.00007697513,0.00003549902,0.000016888369,0.000084966916,0.000046342477],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00060030544,0.0012360711,0.0007254612,0.0015622348,0.00022950431,0.0008057024,0.0007385464,0.00078239915,0.070437856],"category_scores_gemma":[0.00071879313,0.00035532293,0.00035197847,0.00069758686,0.00034386994,0.0008190325,0.00087365275,0.0014478548,0.03544857],"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":[0.000070875474,0.00005562512,0.000073503346,0.0008868577,0.000010541613,0.00015336867,0.00004222875,0.00012502172,0.00071159925,0.0008447602,0.30128095,0.69574463],"study_design_scores_gemma":[0.00002574526,0.000068082605,0.0009935418,0.0008168721,0.000008738158,0.0011768893,0.000060037954,0.00013393053,0.00031417434,0.0013140856,0.9950748,0.000013069403],"about_ca_topic_score_codex":0.0024408498,"about_ca_topic_score_gemma":0.0065913796,"teacher_disagreement_score":0.070437856,"about_ca_system_score_codex":0.00037608162,"about_ca_system_score_gemma":0.0006052765,"threshold_uncertainty_score":0.23563808},"labels":[],"label_agreement":null},{"id":"W2328600316","doi":"10.1016/j.jcjd.2013.03.337","title":"Investigating Food Choice and Food-Related Problems in Individuals Living with Prader-Willi Syndrome","year":2013,"lang":"en","type":"article","venue":"Canadian Journal of Diabetes","topic":"Genetic Syndromes and Imprinting","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":true,"route_about_ca":false,"ca_institutions":"Kelowna General Hospital","funders":"","keywords":"Medicine; Obesity; Food choice; Caloric theory; Disease; Developmental psychology; Clinical psychology; Psychology; Endocrinology; Internal medicine","score_opus":0.009067810950848488,"score_gpt":0.18552140524191701,"score_spread":0.17645359429106852,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2328600316","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99953866,0.00006177288,0.000022210705,0.000021678923,0.000002101978,0.0000084713265,0.00005244321,0.0000011355608,0.00029143025],"genre_scores_gemma":[0.99922013,0.00011139038,0.00017766992,0.000036934944,0.00000278817,0.000009299353,0.00007324001,0.000001184379,0.00036747087],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9996568,0.000093902236,0.00004364349,0.00005881668,0.00007731602,0.000069553134],"domain_scores_gemma":[0.99959415,0.00009256845,0.00011952146,0.000017852508,0.000062629995,0.00011320209],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0004140591,0.0004241141,0.00037961322,0.0013340184,0.0010981251,0.00049378496,0.0003353933,0.0004970033,0.000996079],"category_scores_gemma":[0.0015585849,0.0002369884,0.00048343942,0.0009846448,0.00040520474,0.0003259954,0.0005748429,0.00060929335,0.00016004448],"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":[0.0000915942,0.00012508238,0.9949184,0.000012853549,0.000035238027,0.0012131039,0.0006153248,0.000038917027,0.0009495862,0.000019163792,0.00004017035,0.0019404711],"study_design_scores_gemma":[0.000005289567,0.00033129883,0.99514294,0.0000055847017,0.000033394706,0.0025216015,0.0014213048,0.000109271285,0.00022758111,0.000041793814,0.00015263098,0.0000073795372],"about_ca_topic_score_codex":0.024533588,"about_ca_topic_score_gemma":0.031693198,"teacher_disagreement_score":0.024533588,"about_ca_system_score_codex":0.00051236193,"about_ca_system_score_gemma":0.0004437171,"threshold_uncertainty_score":0.048781574},"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":"observational","genre":"empirical","about_ca_system":false,"about_ca_topic":false,"confidence":"low"}],"label_agreement":"agree"},{"id":"W2334848682","doi":"10.1515/jpem.2004.17.9.1215","title":"Lack of Association of Birth Size with Polymorphisms of Two Imprinted Genes, IGF2R and GRB10","year":2004,"lang":"en","type":"article","venue":"Journal of Pediatric Endocrinology and Metabolism","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":10,"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":"Genomic imprinting; Linkage disequilibrium; Allele; Genetics; Single-nucleotide polymorphism; SNP; Imprinting (psychology); Genotype; Gene; Medicine; Genetic association; Insulin-like growth factor 2 receptor; Biology; Insulin-like growth factor 1 receptor","score_opus":0.009059304429495851,"score_gpt":0.24769438171630606,"score_spread":0.23863507728681022,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2334848682","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9991793,0.00016244593,0.00021177993,0.000034558117,0.0000049962528,0.0000016460815,0.00012964293,0.0000070364786,0.0002686446],"genre_scores_gemma":[0.99926466,0.00009277838,0.00013928044,0.000011522955,0.000005554914,0.0000034186753,0.00017398737,0.0000058380124,0.0003029362],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9993855,0.00011898524,0.00007116312,0.00020083711,0.0001526321,0.00007089271],"domain_scores_gemma":[0.99675506,0.0014694756,0.0008907785,0.0004707351,0.00010303999,0.00031093878],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00067619653,0.0002843254,0.0004157182,0.0007869619,0.00018474087,0.0003068773,0.0005373742,0.0003498396,0.0026484292],"category_scores_gemma":[0.0031645182,0.00021684902,0.00026436764,0.00046176318,0.0006562649,0.0001643424,0.0003948104,0.00047298518,0.00022494594],"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":[0.00080097164,0.000038455506,0.97087854,0.00004225498,0.00019629872,0.001153381,0.0002215557,0.000120638244,0.021007475,0.00020445502,0.00006814696,0.005267863],"study_design_scores_gemma":[0.000011327904,0.00020148992,0.9946085,0.0000063772286,0.00004611537,0.0031510335,0.000074829215,0.00017767864,0.0013865856,0.00010128353,0.00023102498,0.0000038410076],"about_ca_topic_score_codex":0.0010091211,"about_ca_topic_score_gemma":0.0009168163,"teacher_disagreement_score":0.0026484292,"about_ca_system_score_codex":0.00021268953,"about_ca_system_score_gemma":0.00020683286,"threshold_uncertainty_score":0.008859932},"labels":[],"label_agreement":null},{"id":"W2342794187","doi":"10.14740/jem.v6i2.337","title":"Clinical and Genetic Study of Pseudohypoparathyroidism Type 1b in Hong Kong Chinese","year":2016,"lang":"en","type":"article","venue":"Journal of Endocrinology and Metabolism","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":0,"is_retracted":false,"has_abstract":true,"route_ca_aff":false,"route_ca_fund":false,"route_ca_venue":true,"route_about_ca":false,"ca_institutions":"","funders":"","keywords":"GNAS complex locus; Pseudohypoparathyroidism; Medicine; Uniparental disomy; Imprinting (psychology); Multiplex ligation-dependent probe amplification; Genetics; Chinese population; Locus (genetics); Gene; Bioinformatics; Chromosome; Internal medicine; Parathyroid hormone; Karyotype; Biology; Genotype; Exon","score_opus":0.016792506397998935,"score_gpt":0.30657542035166213,"score_spread":0.2897829139536632,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2342794187","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99936503,0.00012401289,0.00005007383,0.000038825947,0.000003435918,0.000013063437,0.000048587684,0.0000015888454,0.00035532718],"genre_scores_gemma":[0.9995228,0.0001120585,0.000042239266,0.000027596821,0.0000046495707,0.000004292713,0.000046142435,0.0000013335238,0.00023890314],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9997677,0.00002783542,0.000036656937,0.00007189486,0.000042297674,0.000053543612],"domain_scores_gemma":[0.99962866,0.000065499305,0.00006902954,0.000021742206,0.000046778954,0.00016824734],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00021594428,0.00045496406,0.00042166232,0.0011677503,0.0012795407,0.0003173384,0.0002730484,0.00037257056,0.0012261763],"category_scores_gemma":[0.0007031146,0.00035511176,0.00026962822,0.0013304176,0.0005964413,0.00026226556,0.00045555836,0.00026535752,0.00012375716],"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":[0.00014803308,0.000088168286,0.9202971,0.000049974584,0.00004301883,0.068746,0.002410995,0.0001121956,0.005304468,0.000114872884,0.00019697401,0.0024883328],"study_design_scores_gemma":[0.000017463019,0.00016349426,0.95949405,0.000013652024,0.00005385713,0.03746125,0.0014843475,0.00031545616,0.00044377084,0.000060667873,0.00047233756,0.000019694886],"about_ca_topic_score_codex":0.089108266,"about_ca_topic_score_gemma":0.043796636,"teacher_disagreement_score":0.089108266,"about_ca_system_score_codex":0.00095585163,"about_ca_system_score_gemma":0.00080076087,"threshold_uncertainty_score":0.17717916},"labels":[],"label_agreement":null},{"id":"W2343776705","doi":"10.1016/j.soard.2016.04.023","title":"Sleeve gastrectomy leads to weight loss in the Magel2 knockout mouse","year":2016,"lang":"en","type":"article","venue":"Surgery for Obesity and Related Diseases","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":16,"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","funders":"National Institute of Diabetes and Digestive and Kidney Diseases; Canadian Institutes of Health Research; National Institutes of Health","keywords":"Medicine; Weight loss; Internal medicine; Obesity; Sleeve gastrectomy; Endocrinology; Lean body mass; Knockout mouse; Weight gain; Body weight; Gastric bypass","score_opus":0.006801932565752736,"score_gpt":0.2175652416658789,"score_spread":0.21076330910012617,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2343776705","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9907755,0.0007449441,0.004374285,0.0004161428,0.00014574848,0.000034810048,0.0016621703,0.00052643346,0.001319937],"genre_scores_gemma":[0.97785485,0.0012987083,0.004559165,0.00023054075,0.00007807461,0.000119716286,0.00143157,0.00049968634,0.01392766],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9995598,0.000046942783,0.000053703625,0.00013157245,0.00013201058,0.00007593718],"domain_scores_gemma":[0.99923086,0.0001146428,0.00027994465,0.0000586637,0.000023217202,0.0002926245],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00039020096,0.0014762931,0.0007446936,0.0017380806,0.00040672833,0.0008271821,0.0006313066,0.001502239,0.0046052947],"category_scores_gemma":[0.00034739514,0.0008053385,0.0008479026,0.00049681525,0.0012142197,0.00051974907,0.00083167996,0.0019181508,0.0011678876],"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":[0.00050296576,0.00008134016,0.0003602939,0.000041868007,0.00002483869,0.00061745476,0.000034976427,0.00019121694,0.99668044,0.00042792814,0.00012627343,0.0009103616],"study_design_scores_gemma":[0.00047124122,0.0007205931,0.017844718,0.000059861053,0.00020078564,0.0047937306,0.00022700215,0.003246433,0.9657231,0.0006694032,0.0059820963,0.00006108701],"about_ca_topic_score_codex":0.00060981826,"about_ca_topic_score_gemma":0.001308427,"teacher_disagreement_score":0.0046052947,"about_ca_system_score_codex":0.0004739221,"about_ca_system_score_gemma":0.00033931425,"threshold_uncertainty_score":0.015406251},"labels":[],"label_agreement":null},{"id":"W2344998708","doi":"10.1242/dev.129.7.1657","title":"Disruption of mesodermal enhancers for<i>Igf2</i>in the minute mutant","year":2002,"lang":"en","type":"article","venue":"Development","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":42,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"St Joseph's Health Care; Lawson Health Research Institute","funders":"","keywords":"Biology; Genomic imprinting; Enhancer; DNA methylation; Genetics; Methylation; Gene silencing; Mutant; Gene; Cell biology; Gene expression","score_opus":0.019845530644543925,"score_gpt":0.2398604491141757,"score_spread":0.22001491846963178,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2344998708","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99339384,0.00028899632,0.0047163833,0.000041985862,0.000019815836,0.000013313038,0.0002375587,0.00014083937,0.0011473071],"genre_scores_gemma":[0.9940638,0.00026506212,0.0031876357,0.00001744555,0.0000056114663,0.000018091921,0.00028185273,0.00006396831,0.0020967072],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9999217,0.000010505598,0.000008909169,0.000017815526,0.000025157486,0.000015911966],"domain_scores_gemma":[0.99987006,0.000025746855,0.000058803536,0.000012165375,0.0000036844297,0.000029609644],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00006934697,0.00040557652,0.00011409018,0.00023797674,0.00015479363,0.00018726867,0.00025963533,0.00024361927,0.0010699813],"category_scores_gemma":[0.00011917406,0.00020114642,0.00021138633,0.00009201512,0.0002615013,0.000092853545,0.00030254014,0.00033863963,0.0003471323],"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":[0.00003454994,0.000004046459,0.00015752399,0.000008594995,0.000002674365,0.00009848061,0.000009906165,0.000037348454,0.9987839,0.00020311822,0.000013255852,0.0006466066],"study_design_scores_gemma":[0.000019626146,0.00010094464,0.006132928,0.0000058721484,0.000017100183,0.0009838182,0.000021730628,0.000540686,0.9890531,0.00011199755,0.0030058003,0.000006557205],"about_ca_topic_score_codex":0.0005638169,"about_ca_topic_score_gemma":0.0014583111,"teacher_disagreement_score":0.0010699813,"about_ca_system_score_codex":0.00020308995,"about_ca_system_score_gemma":0.00013433736,"threshold_uncertainty_score":0.0035794973},"labels":[],"label_agreement":null},{"id":"W2345654030","doi":"10.1371/journal.pgen.1005993","title":"Parental Origin of Interstitial Duplications at 15q11.2-q13.3 in Schizophrenia and Neurodevelopmental Disorders","year":2016,"lang":"en","type":"article","venue":"PLoS Genetics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":99,"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; Centre for Addiction and Mental Health","funders":"European Commission; Canadian Institutes of Health Research; National Institute for Health and Care Research; Innovative Medicines Initiative; Genetics Society; National Institute of Mental Health; Medical Research Council; European Federation of Pharmaceutical Industries and Associations","keywords":"Biology; Gene duplication; Angelman syndrome; Genetics; Copy-number variation; Offspring; Population; Schizophrenia (object-oriented programming); Autism; Segmental duplication; Neurodevelopmental disorder; Gene; Pregnancy; Genome; Psychology; Medicine; Psychiatry","score_opus":0.01100033361773941,"score_gpt":0.2301001261174353,"score_spread":0.21909979249969588,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2345654030","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.998604,0.0005683465,0.00034452192,0.00001890734,0.0000048092693,0.0000040904656,0.00015601816,0.0000080623095,0.00029131578],"genre_scores_gemma":[0.99938035,0.0002266611,0.00015897125,0.000010684215,0.0000042878914,0.0000030643562,0.00013111922,0.0000041999742,0.00008070898],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99942625,0.00012284385,0.00007466077,0.00020209978,0.000095156676,0.00007891602],"domain_scores_gemma":[0.998814,0.00033819675,0.000490733,0.0001304178,0.0000659684,0.00016081947],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00047967842,0.00038529883,0.0003453729,0.0014307103,0.00030999043,0.00035043477,0.00026603465,0.00029196264,0.0020952984],"category_scores_gemma":[0.0018677545,0.00022794286,0.00043702102,0.0008570281,0.0004536389,0.0002051328,0.00067401835,0.00026133232,0.0001978502],"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":[0.00067532586,0.00002921187,0.9602827,0.00006474302,0.00017545685,0.004386679,0.00072064676,0.00014266829,0.023634886,0.00022448893,0.00010237627,0.009560881],"study_design_scores_gemma":[0.000014551628,0.000088551766,0.99165535,0.00002101879,0.00013459758,0.005391595,0.00019625056,0.00013410326,0.001819481,0.00017509138,0.00035974247,0.000009696165],"about_ca_topic_score_codex":0.0035595412,"about_ca_topic_score_gemma":0.0049807806,"teacher_disagreement_score":0.0035595412,"about_ca_system_score_codex":0.00022738913,"about_ca_system_score_gemma":0.00034502894,"threshold_uncertainty_score":0.0070776343},"labels":[],"label_agreement":null},{"id":"W2345760292","doi":"10.1007/s00439-016-1675-5","title":"The expanding phenotypic spectrum of female SLC9A6 mutation carriers: a case series and review of the literature","year":2016,"lang":"en","type":"review","venue":"Human Genetics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":42,"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; Lakeridge Health; Hospital for Sick Children","funders":"","keywords":"Biology; Intellectual disability; Phenotype; Microcephaly; Genetics; Mutation; Angelman syndrome; Rett syndrome; Fragile X syndrome; UBE3A; Gene","score_opus":0.02066044893561742,"score_gpt":0.30338355180319254,"score_spread":0.2827231028675751,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2345760292","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":[0.007378265,0.9880525,0.00063824066,0.00094069773,0.00024576337,0.000009828088,0.000105716426,0.000030444819,0.002598632],"genre_scores_gemma":[0.039074108,0.95649135,0.0013398015,0.00092458335,0.0008814736,0.0000105152385,0.0001812555,0.000013708063,0.0010831908],"study_design_codex":"design_other","study_design_gemma":"case_report","domain_scores_codex":[0.99977976,0.000029814715,0.00006733931,0.000049213195,0.000048434602,0.000025468047],"domain_scores_gemma":[0.9994966,0.0002648595,0.000118496675,0.000018094184,0.00005789089,0.000043994303],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00031062143,0.0008157301,0.0013780993,0.003266572,0.00029366135,0.0010382438,0.0007050131,0.001079593,0.0020685105],"category_scores_gemma":[0.0010705705,0.00021755522,0.00049208547,0.00227913,0.00055245863,0.0012370222,0.0006188582,0.00072743313,0.0006156036],"study_design_candidate":"case_report","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00014416927,0.00007565367,0.010780736,0.012294363,0.00024368436,0.24333128,0.0005229738,0.00052297825,0.00819734,0.0018120684,0.022960145,0.6991146],"study_design_scores_gemma":[0.000017998926,0.000049784103,0.008337813,0.004184561,0.0004303517,0.81189495,0.00045480212,0.00018863604,0.0010824774,0.0016504022,0.17164968,0.00005850899],"about_ca_topic_score_codex":0.00064760994,"about_ca_topic_score_gemma":0.001296983,"teacher_disagreement_score":0.003266572,"about_ca_system_score_codex":0.00028849803,"about_ca_system_score_gemma":0.00056676386,"threshold_uncertainty_score":0.006919861},"labels":[],"label_agreement":null},{"id":"W2346557592","doi":"10.1186/s13148-016-0215-4","title":"Kaiso mediates human ICR1 methylation maintenance and H19 transcriptional fine regulation","year":2016,"lang":"en","type":"article","venue":"Clinical Epigenetics","topic":"Genetic Syndromes and Imprinting","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":"McGill University Health Centre","funders":"Studienstiftung des Deutschen Volkes; Bundesministerium für Bildung und Forschung","keywords":"CTCF; Genomic imprinting; DNA methylation; Biology; Transcription factor; Epigenetics; Imprinting (psychology); Chromatin; CRISPR; Methylation; Genetics; Chromatin immunoprecipitation; Enhancer; Promoter; Gene; Gene expression","score_opus":0.03547001202568329,"score_gpt":0.3256148072426463,"score_spread":0.290144795216963,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2346557592","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.984124,0.003367901,0.0057209586,0.00017103065,0.00004007566,0.000036995203,0.00067692494,0.00032977492,0.0055322954],"genre_scores_gemma":[0.99347174,0.0005202852,0.0013213982,0.00004238872,0.000012073587,0.000016960543,0.0008672488,0.000038280486,0.0037096334],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9998369,0.000011269219,0.0000060028833,0.0000604544,0.000037921738,0.000047508114],"domain_scores_gemma":[0.99985945,0.000017730179,0.00004994562,0.000018239552,0.000013391614,0.00004125328],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00011742392,0.00048470584,0.00018069457,0.00027340453,0.00025730042,0.0003475318,0.0005372508,0.0002967547,0.0042651733],"category_scores_gemma":[0.00021076707,0.00020406183,0.00030016186,0.00010898708,0.0003030202,0.00018363287,0.0003880439,0.00042170752,0.0019644352],"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":[0.00010712379,0.0000107799,0.0003694663,0.000040635765,0.0000059168374,0.00005763732,0.000014381707,0.000034426794,0.99813724,0.00010049558,0.00007280344,0.0010490222],"study_design_scores_gemma":[0.000021771295,0.00011316552,0.019459575,0.000008992119,0.000019621793,0.0006102279,0.000045595552,0.00076088746,0.97393143,0.000095536605,0.0049245213,0.000008636797],"about_ca_topic_score_codex":0.00095971854,"about_ca_topic_score_gemma":0.0013312667,"teacher_disagreement_score":0.0042651733,"about_ca_system_score_codex":0.00047074404,"about_ca_system_score_gemma":0.0002162288,"threshold_uncertainty_score":0.014268398},"labels":[],"label_agreement":null},{"id":"W2360837375","doi":"10.1016/j.fertnstert.2016.04.036","title":"Altered DNA methylation and expression of PLAGL1 in cord blood from assisted reproductive technology pregnancies compared with natural conceptions","year":2016,"lang":"en","type":"article","venue":"Fertility and Sterility","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","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":"University of British Columbia","funders":"Division of Materials Research; Canadian Institutes of Health Research","keywords":"DNA methylation; Genomic imprinting; Cord blood; Epigenetics; Biology; Andrology; Methylation; Methylated DNA immunoprecipitation; Placenta; Differentially methylated regions; Molecular biology; Genetics; Gene expression; Gene; Fetus; Pregnancy; Medicine","score_opus":0.016758465906837137,"score_gpt":0.24634008863740597,"score_spread":0.22958162273056884,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2360837375","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99868363,0.0003314452,0.00030835546,0.000021597756,0.000004672125,0.0000030429972,0.00019645065,0.000008879904,0.00044198002],"genre_scores_gemma":[0.99862945,0.00017291203,0.00022672224,0.000017857761,0.0000042464026,0.000006873595,0.0002391841,0.000004250454,0.00069839164],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9999168,0.000014036595,0.0000057490593,0.000024730985,0.000021419013,0.000017278979],"domain_scores_gemma":[0.9998801,0.0000330607,0.000034706845,0.000011979367,0.000014042974,0.000026106918],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.000114542236,0.00007331718,0.00010942122,0.00047528604,0.00014621962,0.00020148982,0.0001399137,0.00013231573,0.0015155019],"category_scores_gemma":[0.00047845845,0.00008682037,0.00008028574,0.00023067182,0.00016222839,0.0000653199,0.00012819692,0.0001918214,0.00014806165],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0018104904,0.000055654127,0.10347679,0.000049226666,0.00005485172,0.0006563199,0.0004522485,0.00009610303,0.8805415,0.00015070272,0.00016518278,0.012490895],"study_design_scores_gemma":[0.000019597375,0.0003071653,0.78901786,0.000010615586,0.00005490934,0.0029959932,0.00037161118,0.0005201888,0.20519027,0.00016372978,0.0013392906,0.000008729761],"about_ca_topic_score_codex":0.0019686231,"about_ca_topic_score_gemma":0.0014533914,"teacher_disagreement_score":0.0019686231,"about_ca_system_score_codex":0.00013870714,"about_ca_system_score_gemma":0.0001153176,"threshold_uncertainty_score":0.005069852},"labels":[],"label_agreement":null},{"id":"W2375961688","doi":"10.1038/ejhg.2016.45","title":"EMQN best practice guidelines for the molecular genetic testing and reporting of chromosome 11p15 imprinting disorders: Silver–Russell and Beckwith–Wiedemann syndrome","year":2016,"lang":"en","type":"article","venue":"European Journal of Human Genetics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":86,"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; University of Toronto","funders":"Bundesministerium für Bildung und Forschung","keywords":"Beckwith–Wiedemann syndrome; Imprinting (psychology); Guideline; Best practice; Genetic testing; Context (archaeology); Snapshot (computer storage); Genomic imprinting; Medicine; Psychology; Computer science; Genetics; Biology; Political science; Pathology; Gene; Law","score_opus":0.053850792924303593,"score_gpt":0.3185356653326078,"score_spread":0.2646848724083042,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2375961688","genre_codex":"commentary","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":[0.0076146577,0.08360731,0.30256975,0.42354685,0.0373962,0.017745078,0.011434914,0.005811058,0.11027423],"genre_scores_gemma":[0.03158521,0.07297028,0.6740931,0.117454514,0.009151111,0.025267903,0.021063931,0.0021788739,0.046235103],"study_design_codex":"not_applicable","study_design_gemma":"not_applicable","domain_scores_codex":[0.8559184,0.06899097,0.042372927,0.0038586878,0.025412945,0.003446051],"domain_scores_gemma":[0.67864275,0.1082229,0.024990635,0.015800463,0.16458015,0.007763073],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.11504695,0.0014949562,0.0027788458,0.010508271,0.0024262918,0.006321393,0.009901012,0.015971782,0.010362992],"category_scores_gemma":[0.2584122,0.0017301522,0.005392137,0.006778105,0.0053543802,0.0043985443,0.005851361,0.010388897,0.011956202],"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":[0.00026791127,0.00039903933,0.0030140912,0.0068408772,0.00018782521,0.002189136,0.0031593833,0.0017856903,0.003111161,0.01931525,0.7421647,0.217565],"study_design_scores_gemma":[0.00018984734,0.00015410916,0.006232559,0.017505627,0.00017539314,0.0029979146,0.0013167434,0.0011522375,0.0018167637,0.01747794,0.9507957,0.00018525227],"about_ca_topic_score_codex":0.016929802,"about_ca_topic_score_gemma":0.016082166,"teacher_disagreement_score":0.11504695,"about_ca_system_score_codex":0.005953391,"about_ca_system_score_gemma":0.02645497,"threshold_uncertainty_score":0.6084337},"labels":[],"label_agreement":null},{"id":"W2395063123","doi":"10.1371/journal.pgen.1006062","title":"Angelman Syndrome Protein Ube3a Regulates Synaptic Growth and Endocytosis by Inhibiting BMP Signaling in Drosophila","year":2016,"lang":"en","type":"article","venue":"PLoS Genetics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":61,"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; Ministry of Science and Technology; National Science Foundation; National Institutes of Health; Chinese Academy of Sciences","keywords":"UBE3A; Biology; Cell biology; Ubiquitin ligase; Angelman syndrome; Bone morphogenetic protein; Ubiquitin; Endocytosis; F-box protein; BMPR2; Genetics; Receptor","score_opus":0.00981467043920895,"score_gpt":0.2027767330921121,"score_spread":0.19296206265290317,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2395063123","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9942173,0.001479505,0.0022620466,0.000095094125,0.000020361611,0.000009741409,0.0004269406,0.00010696902,0.001382021],"genre_scores_gemma":[0.9957449,0.0005615283,0.001368848,0.00003092697,0.000003097223,0.000012058484,0.00024896525,0.000022593706,0.00200708],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9999291,0.000009437834,0.000008423743,0.000015654337,0.000023492457,0.00001384211],"domain_scores_gemma":[0.99993646,0.000007591166,0.000024772686,0.0000049321065,0.0000054067436,0.000020810938],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00008070124,0.00038721616,0.00013527961,0.00030984243,0.00017024504,0.0002074457,0.00016566856,0.00023023084,0.0007598624],"category_scores_gemma":[0.00007653076,0.00017098704,0.00025150072,0.000107257176,0.00024216957,0.00012670815,0.00020692933,0.00029669786,0.00034847102],"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":[0.000035886143,0.0000052101145,0.0002835074,0.000014625929,0.000004564426,0.000112805654,0.0000058853607,0.00005520042,0.9989084,0.00011191809,0.000028045506,0.00043399018],"study_design_scores_gemma":[0.000028885015,0.00007095295,0.024583906,0.000012159718,0.000032044747,0.001022536,0.000043976605,0.003934241,0.96647435,0.00022817601,0.0035599333,0.000008761465],"about_ca_topic_score_codex":0.0016818686,"about_ca_topic_score_gemma":0.0029882793,"teacher_disagreement_score":0.0016818686,"about_ca_system_score_codex":0.00047224184,"about_ca_system_score_gemma":0.00020561846,"threshold_uncertainty_score":0.0034264326},"labels":[],"label_agreement":null},{"id":"W2402010036","doi":"10.1016/j.jtho.2016.05.010","title":"ITPKA Gene Body Methylation Regulates Gene Expression and Serves as an Early Diagnostic Marker in Lung and Other Cancers","year":2016,"lang":"en","type":"article","venue":"Journal of Thoracic Oncology","topic":"Genetic Syndromes and Imprinting","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":"BC Cancer Agency","funders":"National Cancer Institute","keywords":"Medicine; Methylation; Gene; DNA methylation; Lung cancer; Gene expression; Cancer research; Lung; Genetics; Pathology; Internal medicine; Biology","score_opus":0.010288991759806392,"score_gpt":0.3360287557402515,"score_spread":0.3257397639804451,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2402010036","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9911398,0.002329507,0.002779317,0.00016520923,0.000027916678,0.000013792635,0.00061641354,0.00012359531,0.0028044272],"genre_scores_gemma":[0.9973199,0.0004989833,0.00095536554,0.000020273259,0.000009038574,0.000006748263,0.0002143791,0.000014889007,0.000960339],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.99985623,0.000023695837,0.000011881666,0.000044182387,0.000034827503,0.000029108958],"domain_scores_gemma":[0.9998109,0.00003957223,0.00007277886,0.0000194315,0.000022962093,0.000034262885],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00015650694,0.00021659443,0.00021458532,0.0006981851,0.00023834528,0.00045097672,0.00019223703,0.00026095906,0.0016178694],"category_scores_gemma":[0.00035168967,0.00020271406,0.00018633252,0.00041159434,0.00029558205,0.000302043,0.00028074044,0.0004127389,0.00040738785],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0011052362,0.000044847206,0.15689498,0.00009523725,0.000050523573,0.0014598639,0.00015304437,0.00024793766,0.8202954,0.0006442398,0.0002967103,0.018711846],"study_design_scores_gemma":[0.000026528676,0.00022403924,0.60624766,0.000022206204,0.00013617227,0.0069465274,0.0002775851,0.0018005759,0.37841094,0.00087435835,0.005014517,0.000018802788],"about_ca_topic_score_codex":0.00081906805,"about_ca_topic_score_gemma":0.0009096785,"teacher_disagreement_score":0.0016178694,"about_ca_system_score_codex":0.00029568974,"about_ca_system_score_gemma":0.0002013166,"threshold_uncertainty_score":0.00541234},"labels":[],"label_agreement":null},{"id":"W2403173295","doi":"10.1038/gim.2016.53","title":"The phenotypic spectrum of Schaaf-Yang syndrome: 18 new affected individuals from 14 families","year":2016,"lang":"en","type":"article","venue":"Genetics in Medicine","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":122,"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; Children's & Women's Health Centre of British Columbia; Centre Hospitalier Universitaire de Sherbrooke","funders":"Eunice Kennedy Shriver National Institute of Child Health and Human Development; Intellectual and Developmental Disabilities Research Center; Foundation for Prader-Willi Research","keywords":"Genetics; Hypotonia; Phenotype; Allele; Autism spectrum disorder; Intellectual disability; Disease; Context (archaeology); Biology; Gene; Medicine; Autism; Internal medicine","score_opus":0.013843740163734906,"score_gpt":0.2566116621732599,"score_spread":0.24276792200952502,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2403173295","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99774337,0.00022160886,0.0005872305,0.00005556763,0.0000059805757,0.000023585044,0.00012693589,0.000020996227,0.0012148104],"genre_scores_gemma":[0.99800736,0.00023261037,0.0006856361,0.000039492446,0.000018623183,0.000035174286,0.00017951644,0.000017009434,0.00078451703],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99929285,0.00012389496,0.0000970867,0.00018556936,0.00017463713,0.00012599445],"domain_scores_gemma":[0.99922216,0.00030347158,0.00013600191,0.000056316818,0.0000863124,0.0001956779],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00044576093,0.002566044,0.0011785591,0.0024039987,0.0016885574,0.000589429,0.00076222746,0.0006500472,0.005331343],"category_scores_gemma":[0.0024479819,0.0007978422,0.0005345076,0.0013187678,0.0017974534,0.00054988154,0.0017649939,0.0005309026,0.000602593],"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":[0.00095519534,0.0005718901,0.53334785,0.00013074768,0.000296491,0.38372177,0.011978101,0.0009821753,0.024487324,0.0010064647,0.0010647913,0.041457217],"study_design_scores_gemma":[0.00015671356,0.00081169483,0.40379465,0.00006967106,0.000361597,0.58124936,0.0029662487,0.00074705837,0.0035441339,0.0014164157,0.0047527333,0.0001297866],"about_ca_topic_score_codex":0.0022153512,"about_ca_topic_score_gemma":0.0017114207,"teacher_disagreement_score":0.005331343,"about_ca_system_score_codex":0.00036745658,"about_ca_system_score_gemma":0.0003543723,"threshold_uncertainty_score":0.01783508},"labels":[],"label_agreement":null},{"id":"W246072","doi":"10.1385/1-59259-300-3:291","title":"Molecular Detection of Uniparental Disomy","year":2003,"lang":"en","type":"article","venue":"Molecular Cytogenetics","topic":"Genetic Syndromes and Imprinting","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":"University of British Columbia","funders":"","keywords":"Uniparental disomy; Genetics; Biology; Genotyping; Microsatellite; Imprinting (psychology); Karyotype; Genomic imprinting; DNA methylation; Chromosome; Genotype; Gene; Allele","score_opus":0.007801442593724252,"score_gpt":0.22665746649278531,"score_spread":0.21885602389906106,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W246072","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.712488,0.020894976,0.19690408,0.0017330197,0.00074717304,0.0006966345,0.009083883,0.0030158237,0.054436427],"genre_scores_gemma":[0.78106284,0.013563499,0.15802798,0.0010796705,0.00020220023,0.0007483061,0.009767912,0.00019857033,0.0353489],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9994815,0.000099490884,0.000047717043,0.00014361378,0.00015560775,0.000072177194],"domain_scores_gemma":[0.99932146,0.000192776,0.00011893474,0.00006503812,0.00018724431,0.000114598646],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.000660591,0.00043155457,0.00045902425,0.002723533,0.0002010494,0.0004191965,0.0006909045,0.0008295335,0.007757001],"category_scores_gemma":[0.0012164095,0.00034138633,0.0002640608,0.0006798788,0.00028567069,0.00038426826,0.0004058571,0.0007738873,0.004015887],"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":[0.00013042358,0.00004436808,0.0057501146,0.0002342532,0.000036634454,0.00075989804,0.00009177249,0.000069818365,0.965207,0.0011608656,0.0013118251,0.025203004],"study_design_scores_gemma":[0.00006211419,0.0008210039,0.112491906,0.00017332692,0.00015199116,0.013857595,0.0002873883,0.0031702158,0.7940104,0.0027064634,0.072215945,0.00005158004],"about_ca_topic_score_codex":0.00028341686,"about_ca_topic_score_gemma":0.00058823917,"teacher_disagreement_score":0.007757001,"about_ca_system_score_codex":0.00019389731,"about_ca_system_score_gemma":0.0001221075,"threshold_uncertainty_score":0.025949776},"labels":[],"label_agreement":null},{"id":"W2464134108","doi":"10.2217/epi-2016-0007","title":"Phenotypic Spectrum and Extent of DNA Methylation Defects Associated with Multilocus Imprinting Disturbances","year":2016,"lang":"en","type":"article","venue":"Epigenomics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":30,"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","keywords":"Biology; Imprinting (psychology); DNA methylation; Genetics; Phenotype; Genomic imprinting; Epigenetics; Methylation; DNA; Computational biology; Evolutionary biology; Gene; Gene expression","score_opus":0.00778595025884418,"score_gpt":0.2124860684525933,"score_spread":0.20470011819374911,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2464134108","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9988404,0.00018809752,0.000440527,0.0000138319065,0.000001131751,0.000004168599,0.00025775132,0.000011537213,0.00024255562],"genre_scores_gemma":[0.9994351,0.00006390524,0.00021900814,0.0000060013344,0.0000015685141,0.000003207119,0.00017366507,0.000003249634,0.00009419225],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9998167,0.000023710292,0.000019590538,0.00007380992,0.000034113564,0.00003217642],"domain_scores_gemma":[0.9996118,0.000111325586,0.0001669274,0.000030638577,0.000027988382,0.00005129778],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00020617602,0.00039517207,0.00019176635,0.0008253189,0.00013662431,0.00023207975,0.00019623242,0.00023786444,0.0020109478],"category_scores_gemma":[0.00087855913,0.000100776924,0.00016826532,0.00027925087,0.00024144011,0.00010988569,0.0004142772,0.00017794338,0.00019841905],"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":[0.0006495375,0.000025838404,0.8589385,0.000053942636,0.00009617617,0.0024281167,0.00023931502,0.00030532238,0.12525722,0.00013225107,0.000111535664,0.011762356],"study_design_scores_gemma":[0.000014235053,0.00013223133,0.97309387,0.000010267146,0.00006375238,0.011375056,0.00010831508,0.00029974367,0.014412972,0.00010502664,0.00037817468,0.0000063981665],"about_ca_topic_score_codex":0.00070682616,"about_ca_topic_score_gemma":0.00068264664,"teacher_disagreement_score":0.0020109478,"about_ca_system_score_codex":0.00012833683,"about_ca_system_score_gemma":0.0000955258,"threshold_uncertainty_score":0.006727278},"labels":[],"label_agreement":null},{"id":"W2465632847","doi":"10.1080/02701367.2016.1182113","title":"A Characterization of Movement Skills in Obese Children With and Without Prader-Willi Syndrome","year":2016,"lang":"en","type":"article","venue":"Research Quarterly for Exercise and Sport","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":15,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"St. Francis Xavier University","funders":"California State University, Fullerton","keywords":"Normative; Gross motor skill; Motor skill; Movement assessment; Medicine; Psychology; Motor function; Developmental psychology; Physical therapy; Audiology; Physical medicine and rehabilitation","score_opus":0.010247144788470131,"score_gpt":0.2747624842016629,"score_spread":0.2645153394131928,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2465632847","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99962795,0.00005342025,0.00006606096,0.000008483613,0.0000013084549,0.00000437713,0.00007534218,0.0000021037981,0.00016089345],"genre_scores_gemma":[0.99932134,0.00006367289,0.00023618373,0.000009285123,0.000003188299,0.000012738427,0.00023748016,0.0000022618906,0.00011393944],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9997311,0.000040650302,0.000039578812,0.00006848813,0.00007181692,0.00004823892],"domain_scores_gemma":[0.99911994,0.00016104497,0.00045604457,0.000032105796,0.000090456146,0.00014049525],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00038468756,0.000454858,0.00025192334,0.0013968094,0.00018159168,0.00029783745,0.00022809376,0.0002947907,0.0013443115],"category_scores_gemma":[0.0020945577,0.00014000379,0.00019575476,0.00043062298,0.00049883395,0.0003645515,0.000602788,0.00032200827,0.00018712622],"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":[0.0000655673,0.000025995547,0.99466187,0.000018576906,0.00001822194,0.00038753246,0.00016877172,0.000053673786,0.0021951764,0.000027477805,0.000037762966,0.002339509],"study_design_scores_gemma":[0.0000023455048,0.000087753266,0.99775,0.0000043189875,0.0000050229824,0.0016760268,0.00015284836,0.000053669613,0.00019081027,0.000009863659,0.00006553051,0.000001788407],"about_ca_topic_score_codex":0.002626475,"about_ca_topic_score_gemma":0.002491022,"teacher_disagreement_score":0.002626475,"about_ca_system_score_codex":0.00015261283,"about_ca_system_score_gemma":0.00026397596,"threshold_uncertainty_score":0.00522238},"labels":[],"label_agreement":null},{"id":"W2465667391","doi":"10.1093/hmg/ddw181","title":"Genome-wide association study of 40,000 individuals identifies two novel loci associated with bipolar disorder","year":2016,"lang":"en","type":"review","venue":"Human Molecular Genetics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":237,"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; Douglas Mental Health University Institute; McGill University Health Centre; Montreal Neurological Institute and Hospital; Dalhousie University","funders":"Common Fund; National Institute of Neurological Disorders and Stroke; National Cancer Institute; NIH Office of the Director; National Institute of Mental Health; National Heart, Lung, and Blood Institute; National Institute on Drug Abuse; University of Miami; National Alliance for Research on Schizophrenia and Depression; National Institutes of Health; Schweizerischer Nationalfonds zur Förderung der Wissenschaftlichen Forschung; University of Louisville; Ministry of Education, India; Broad Institute; Johns Hopkins University; National Center for Advancing Translational Sciences; National Human Genome Research Institute; Wellcome Trust; University of Pennsylvania; Wayne State University","keywords":"Genome-wide association study; Bipolar disorder; Genetics; Heritability; Biology; Odds ratio; Genetic association; Genotype; Medicine; Single-nucleotide polymorphism; Internal medicine; Gene; Lithium (medication); Endocrinology","score_opus":0.021665797165333386,"score_gpt":0.2920494485161157,"score_spread":0.2703836513507823,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2465667391","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":[0.00045184692,0.9974826,0.00025866827,0.00028511722,0.00010904521,0.000005464014,0.00007464075,0.000012628909,0.0013200118],"genre_scores_gemma":[0.0030600706,0.99557084,0.00033150832,0.00025751692,0.00008847799,0.0000071590835,0.00013931256,0.0000025545542,0.00054269814],"study_design_codex":"design_other","study_design_gemma":"observational","domain_scores_codex":[0.9998099,0.000035270765,0.000029963156,0.00004808604,0.000056534143,0.000020287742],"domain_scores_gemma":[0.99966884,0.00017216678,0.000058626312,0.0000128737765,0.000052616877,0.000034784036],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00074679573,0.00078534934,0.0012883812,0.0020196913,0.00019233566,0.0007289193,0.0005911306,0.00083824457,0.0034071833],"category_scores_gemma":[0.0007580818,0.00018881042,0.00054588506,0.001813608,0.00038583053,0.00039348725,0.00056737143,0.0009174296,0.0016479125],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00014602099,0.000028620008,0.0019771315,0.0074717663,0.00038271715,0.00047892143,0.000034970253,0.00013330657,0.0013537456,0.0013309446,0.012360874,0.97430104],"study_design_scores_gemma":[0.00014848441,0.00028431258,0.027116118,0.009957246,0.0020426374,0.010618013,0.00015758656,0.00016901862,0.0017472686,0.0044107838,0.9432729,0.00007578072],"about_ca_topic_score_codex":0.0013596513,"about_ca_topic_score_gemma":0.0026496842,"teacher_disagreement_score":0.0034071833,"about_ca_system_score_codex":0.00043258324,"about_ca_system_score_gemma":0.0008566484,"threshold_uncertainty_score":0.011398137},"labels":[],"label_agreement":null},{"id":"W2472443615","doi":"10.1037/bne0000150","title":"Dopamine pathway imbalance in mice lacking Magel2, a Prader-Willi syndrome candidate gene.","year":2016,"lang":"en","type":"article","venue":"Behavioral Neuroscience","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":25,"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":"Stollery Children’s Hospital Foundation","keywords":"Dopaminergic; Dopamine; Binge eating; Dopaminergic pathways; Appetite; Psychology; Neuroscience; Eating disorders; Endocrinology; Internal medicine; Medicine; Psychiatry","score_opus":0.02205572228013147,"score_gpt":0.2701116726898296,"score_spread":0.24805595040969813,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2472443615","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.96156144,0.0025120499,0.0044018803,0.000689971,0.00016679267,0.00024868184,0.024335256,0.0007925889,0.005291362],"genre_scores_gemma":[0.9335311,0.005451218,0.013597713,0.00048262492,0.000085948916,0.00068195356,0.01904646,0.00041299604,0.026709959],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9998098,0.000021448895,0.000032293625,0.000065254215,0.000045583813,0.000025669471],"domain_scores_gemma":[0.9995396,0.00008511586,0.0002459914,0.000019614377,0.000017362929,0.00009238297],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00021471365,0.0011909741,0.00044152766,0.0020704917,0.00030270114,0.00046770438,0.00075494754,0.0009620967,0.00766832],"category_scores_gemma":[0.0002593659,0.00038954816,0.00046982936,0.00063465297,0.00058439723,0.00045857247,0.0004824941,0.0008377667,0.0013353168],"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":[0.0009973884,0.0003190013,0.002207349,0.00025290638,0.00010542093,0.002531955,0.00010793409,0.00026694458,0.9839019,0.0008890528,0.0010073169,0.007412767],"study_design_scores_gemma":[0.0016260769,0.0039764666,0.14735743,0.0005825039,0.0009534531,0.02657597,0.0007279646,0.0071596573,0.7583064,0.0018636684,0.05068408,0.00018647492],"about_ca_topic_score_codex":0.0013854958,"about_ca_topic_score_gemma":0.0028020246,"teacher_disagreement_score":0.00766832,"about_ca_system_score_codex":0.00044353754,"about_ca_system_score_gemma":0.0003214194,"threshold_uncertainty_score":0.025653064},"labels":[],"label_agreement":null},{"id":"W2473766466","doi":"10.1007/978-1-62703-011-3_8","title":"Engineering of Large Deletions and Duplications In Vivo","year":2012,"lang":"en","type":"article","venue":"Methods in molecular biology","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":1,"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":"Canadian Institutes of Health Research","keywords":"Limiting; Subcloning; Biology; Insertional mutagenesis; Transgene; Gene; Computational biology; Genetics; Stem cell; Cell biology; Genome; Engineering; Recombinant DNA","score_opus":0.012458061833912133,"score_gpt":0.35242424333669076,"score_spread":0.33996618150277863,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2473766466","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":[0.64590997,0.0017623133,0.34141853,0.0003478557,0.00026274362,0.0006691316,0.002732118,0.0016843429,0.0052129743],"genre_scores_gemma":[0.8209622,0.003946396,0.15477009,0.00018962564,0.00007948042,0.0006576694,0.004288678,0.00086110417,0.014244748],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.999534,0.000114954164,0.00006491697,0.00011778757,0.00011194717,0.000056271143],"domain_scores_gemma":[0.9992879,0.00025048168,0.00019408515,0.00015208413,0.00003665682,0.00007876886],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00066713104,0.000679956,0.0005491527,0.00048922206,0.00021296246,0.00036487656,0.00065313576,0.0007110084,0.002021274],"category_scores_gemma":[0.00053295674,0.0006094388,0.00046193157,0.00027971744,0.0003837356,0.0003113505,0.0007912729,0.0010170334,0.0014950116],"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":[0.000033766148,0.0000192135,0.000067108595,0.00006362821,0.000008718417,0.00013569022,0.000024474268,0.0003349397,0.9962907,0.0005706445,0.000063711166,0.0023875176],"study_design_scores_gemma":[0.000029501436,0.00017760451,0.00067967514,0.000016516768,0.00003600187,0.0010146439,0.000018358187,0.0011723385,0.9847413,0.00023221633,0.011872124,0.00000981198],"about_ca_topic_score_codex":0.0001441944,"about_ca_topic_score_gemma":0.00032046752,"teacher_disagreement_score":0.002021274,"about_ca_system_score_codex":0.00019558497,"about_ca_system_score_gemma":0.0003079268,"threshold_uncertainty_score":0.006761849},"labels":[],"label_agreement":null},{"id":"W2473891204","doi":"10.1002/ajmg.a.37819","title":"Genomic imbalance in the centromeric 11p15 imprinting center in three families: Further evidence of a role for IC2 as a cause of Russell–Silver syndrome","year":2016,"lang":"en","type":"article","venue":"American Journal of Medical Genetics Part A","topic":"Genetic Syndromes and Imprinting","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":"Centre for Global Health Research; SickKids Foundation; Mount Sinai Hospital; Hospital for Sick Children; University of Toronto","funders":"","keywords":"Imprinting (psychology); Genomic imprinting; Epigenetics; Genetics; Biology; Phenotype; DNA methylation; Etiology; Gene; Medicine; Internal medicine; Gene expression","score_opus":0.013388694992727183,"score_gpt":0.27735202652610513,"score_spread":0.263963331533378,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2473891204","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.996003,0.00046981729,0.001213911,0.0002951526,0.000032316915,0.000038898757,0.00016421467,0.00007448051,0.0017082032],"genre_scores_gemma":[0.99737406,0.00039315902,0.0013251742,0.00015103952,0.00006091512,0.000024111394,0.00017725679,0.000030031479,0.00046436675],"study_design_codex":"case_report","study_design_gemma":"observational","domain_scores_codex":[0.99917704,0.00012414281,0.000085919884,0.00024793952,0.00022388174,0.00014109934],"domain_scores_gemma":[0.99871373,0.00045226805,0.00027631858,0.00009781309,0.00008963499,0.000370235],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0004660706,0.0022260319,0.0009431927,0.0025280914,0.0016446383,0.0007329167,0.00090162375,0.0013971912,0.002847018],"category_scores_gemma":[0.0022714324,0.0005937927,0.00083569053,0.0013088008,0.0016630951,0.00040413963,0.0015082016,0.0009870868,0.00033585244],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00046531012,0.00026779674,0.19555585,0.00013333865,0.00017133418,0.7343954,0.00520617,0.00063741265,0.041425664,0.0012114986,0.0009911581,0.01953907],"study_design_scores_gemma":[0.000089722445,0.00031136427,0.17691454,0.000051759314,0.00025865174,0.80442035,0.0008535874,0.0010430347,0.011659505,0.0005979474,0.00371483,0.00008476267],"about_ca_topic_score_codex":0.0056639784,"about_ca_topic_score_gemma":0.0031068334,"teacher_disagreement_score":0.0056639784,"about_ca_system_score_codex":0.0009879924,"about_ca_system_score_gemma":0.00083004666,"threshold_uncertainty_score":0.011262059},"labels":[],"label_agreement":null},{"id":"W2485121654","doi":"10.1016/j.yapd.2016.04.005","title":"Prader Willi Syndrome","year":2016,"lang":"en","type":"review","venue":"Advances in Pediatrics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":83,"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 Hospital; University of Alberta","funders":"Eunice Kennedy Shriver National Institute of Child Health and Human Development; National Center for Research Resources; Canadian Institutes of Health Research","keywords":"Medicine; Insulin resistance; Obesity; Disease; Hypotonia; Bioinformatics; Metabolic syndrome; Diabetes mellitus; Type 2 diabetes; Epidemiology; Internal medicine; Endocrinology; Intensive care medicine; Biology","score_opus":0.01318526558406407,"score_gpt":0.3115986136356986,"score_spread":0.2984133480516345,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2485121654","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":[0.00032987524,0.9916666,0.00085001776,0.00075744244,0.00092359364,0.000008401179,0.00005164144,0.000041641182,0.00537068],"genre_scores_gemma":[0.0029940084,0.990568,0.0011221601,0.00075973885,0.0008689677,0.000011139372,0.00013776352,0.000008514064,0.0035297594],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.9997985,0.000029208328,0.0000240197,0.00004080017,0.00008385219,0.000023558623],"domain_scores_gemma":[0.99983215,0.00007717854,0.000027140084,0.000008893329,0.000027711874,0.000026756927],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00031563724,0.0008548472,0.0010085256,0.00168998,0.00030479138,0.0008402935,0.0008234014,0.00089651847,0.0051608174],"category_scores_gemma":[0.00085527374,0.00020926265,0.00027040258,0.0012588971,0.000631239,0.0008384363,0.0011468444,0.0018612241,0.0024820901],"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":[0.000037850023,0.000025007701,0.00029474104,0.0025226541,0.00004369543,0.002487263,0.000049509446,0.00019375396,0.0016404246,0.003980359,0.039965913,0.94875884],"study_design_scores_gemma":[0.00001566051,0.000018212791,0.0007049986,0.0016086719,0.000078920595,0.017152557,0.000044693552,0.0000566783,0.0006093328,0.0019467658,0.9777475,0.000016059954],"about_ca_topic_score_codex":0.0008568758,"about_ca_topic_score_gemma":0.00157133,"teacher_disagreement_score":0.0051608174,"about_ca_system_score_codex":0.00042341932,"about_ca_system_score_gemma":0.0010189688,"threshold_uncertainty_score":0.017264605},"labels":[],"label_agreement":null},{"id":"W2492410565","doi":"10.1093/hmg/ddw225","title":"Muscle dysfunction caused by loss of<i>Magel2</i>in a mouse model of Prader-Willi and Schaaf-Yang syndromes","year":2016,"lang":"en","type":"article","venue":"Human Molecular Genetics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":47,"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":"","keywords":"Hypotonia; Internal medicine; Endocrinology; Atrophy; Phenotype; Sarcopenia; Biology; Obesity; Lean body mass; Medicine; Gene; Body weight; Genetics","score_opus":0.014592802896699009,"score_gpt":0.23441282972254737,"score_spread":0.21982002682584836,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2492410565","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.97802883,0.0013715676,0.010723401,0.00082328386,0.00020421439,0.00029701178,0.0029100925,0.0007843523,0.0048573175],"genre_scores_gemma":[0.96736866,0.0018236652,0.014309077,0.00035389359,0.00006084788,0.00074774085,0.002478468,0.00030737073,0.012550279],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9992631,0.00015768224,0.00010726498,0.00017572533,0.00017210167,0.00012408331],"domain_scores_gemma":[0.9993666,0.00007268936,0.0002137829,0.00006121204,0.00002949471,0.00025624313],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.000581088,0.001247738,0.00044565514,0.0018371212,0.00060729723,0.0006850815,0.0010171453,0.0017180674,0.0035633116],"category_scores_gemma":[0.00025767577,0.00072604703,0.00081672525,0.0005220601,0.0011962372,0.00062106864,0.00064870145,0.0020642723,0.001305509],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0004629388,0.00024016411,0.000508692,0.0000680957,0.000029974583,0.00058353593,0.000080271166,0.0003991684,0.9946049,0.0012315225,0.0003090056,0.0014816768],"study_design_scores_gemma":[0.00039469742,0.0014693598,0.007324518,0.00007593386,0.0001249588,0.0036371187,0.00016700376,0.0047638826,0.96991324,0.00064401934,0.0114408005,0.000044459586],"about_ca_topic_score_codex":0.0009635166,"about_ca_topic_score_gemma":0.0018328681,"teacher_disagreement_score":0.0035633116,"about_ca_system_score_codex":0.0007696768,"about_ca_system_score_gemma":0.0006600278,"threshold_uncertainty_score":0.011920452},"labels":[],"label_agreement":null},{"id":"W2503979078","doi":"10.1002/ajmg.a.37876","title":"Maternal uniparental disomy for chromosome 6 in a patient with IUGR, ambiguous genitalia, and persistent mullerian structures","year":2016,"lang":"en","type":"review","venue":"American Journal of Medical Genetics Part A","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":22,"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; University of Toronto; University of Alberta; SickKids Foundation; Mount Sinai Hospital","funders":"","keywords":"Uniparental disomy; Karyotype; Biology; SNP array; Testis determining factor; Ambiguous genitalia; Vagina; Chromosome; Genetics; Gynecology; Y chromosome; Medicine; Anatomy; Single-nucleotide polymorphism; Gene; Genotype","score_opus":0.014196344817869353,"score_gpt":0.2866293410021264,"score_spread":0.27243299618425704,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2503979078","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":[0.001053141,0.9965579,0.00023736928,0.00036858805,0.00018699898,0.0000035509524,0.00001876044,0.000016668848,0.0015570369],"genre_scores_gemma":[0.008102278,0.9898217,0.0004146501,0.00035995603,0.00038205282,0.0000050727717,0.000054026594,0.000003829304,0.0008564484],"study_design_codex":"design_other","study_design_gemma":"case_report","domain_scores_codex":[0.999877,0.000017567716,0.000024844789,0.000029873374,0.000035358138,0.00001541857],"domain_scores_gemma":[0.9998136,0.00007997843,0.000047056506,0.0000062301197,0.000022565688,0.000030551702],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00022488074,0.0007273666,0.0009014214,0.002858939,0.00022642444,0.0004916344,0.00061672286,0.0008716929,0.0017072457],"category_scores_gemma":[0.0005299473,0.00018525736,0.0002406509,0.0019316677,0.0005032473,0.00083461177,0.00047818213,0.0008548281,0.0011574241],"study_design_candidate":"case_report","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00007799823,0.000051270432,0.0022458488,0.0070105484,0.00009550247,0.02109315,0.00010925672,0.00023948283,0.00217542,0.0014212548,0.024059419,0.9414209],"study_design_scores_gemma":[0.00003949334,0.00018059423,0.010009399,0.005190574,0.0003508026,0.38434544,0.00029757596,0.00017274331,0.0014584082,0.0019334041,0.5959617,0.0000598358],"about_ca_topic_score_codex":0.0006896976,"about_ca_topic_score_gemma":0.001376726,"teacher_disagreement_score":0.002858939,"about_ca_system_score_codex":0.00027995303,"about_ca_system_score_gemma":0.00058319484,"threshold_uncertainty_score":0.005711317},"labels":[],"label_agreement":null},{"id":"W2510138868","doi":"10.1086/377956","title":"<i>Genomic Imprinting and Kinship</i>. <i>The Rutgers Series in Human Evolution. By </i>David Haig. <i>New Brunswick (New Jersey): Rutgers University Press</i>. $65.00 (hardcover); $29.00 (paper). xiii + 218 p; ill.; index. ISBN: 0–8135–3026–1 (hc); 0–8135–3027–X (pb). 2002.","year":2003,"lang":"en","type":"review","venue":"The Quarterly Review of Biology","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":0,"is_retracted":false,"has_abstract":false,"route_ca_aff":false,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":true,"ca_institutions":"","funders":"","keywords":"Kinship; Library science; Index (typography); History; Genealogy; Anthropology; Sociology; Media studies; Computer science","score_opus":0.012061909293222477,"score_gpt":0.2500481354270149,"score_spread":0.2379862261337924,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2510138868","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":[0.000056584224,0.99411905,0.000224388,0.00088665495,0.0010738159,0.0000037564946,0.00004707727,0.000027885684,0.0035608285],"genre_scores_gemma":[0.0017645066,0.97614515,0.00034904428,0.00074214715,0.0012525608,0.000013902339,0.0001271929,0.000013190064,0.019592354],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.99984515,0.00003067339,0.000015872647,0.000029294388,0.00005893333,0.000020124005],"domain_scores_gemma":[0.9998129,0.000073785006,0.000032257838,0.000012626185,0.00003782991,0.00003068422],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00036862935,0.0016086324,0.0014592807,0.0016989909,0.0002570045,0.0009884052,0.0010277007,0.0009708062,0.02172294],"category_scores_gemma":[0.00080980215,0.0007205053,0.00031658387,0.0025375625,0.0012458456,0.0021371534,0.0008426319,0.0016639077,0.017846214],"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":[0.000052631593,0.000023410521,0.00026411377,0.002219097,0.000050011888,0.00016121357,0.000100874764,0.00026656757,0.0006936841,0.0038223227,0.42241648,0.56992954],"study_design_scores_gemma":[0.000012675464,0.000025666655,0.0015674493,0.0010190953,0.000026693424,0.000995874,0.00009206215,0.000050469236,0.00027244407,0.0075554773,0.98836887,0.000013387461],"about_ca_topic_score_codex":0.0045454386,"about_ca_topic_score_gemma":0.009703747,"teacher_disagreement_score":0.02172294,"about_ca_system_score_codex":0.0011342041,"about_ca_system_score_gemma":0.00086769945,"threshold_uncertainty_score":0.07267046},"labels":[],"label_agreement":null},{"id":"W2510213943","doi":"10.1016/j.placenta.2016.06.204","title":"The expression of imprinted genes in the preeclamptic placenta","year":2016,"lang":"en","type":"article","venue":"Placenta","topic":"Genetic Syndromes and Imprinting","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":"Simon Fraser University","funders":"","keywords":"Medicine; Randomized controlled trial; Abdominal aortic aneurysm; Ultrasonography; Surgery; Abdominal ultrasonography; Radiology; Internal medicine; Aneurysm","score_opus":0.009860331585256224,"score_gpt":0.23785578526263287,"score_spread":0.22799545367737664,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2510213943","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99248695,0.004530021,0.0010546845,0.00014302348,0.000011663738,0.000004213282,0.00015203805,0.000026043232,0.0015913018],"genre_scores_gemma":[0.9975969,0.0014115709,0.00035915792,0.00001639876,0.0000092553555,0.0000032659098,0.000075632684,0.000006026873,0.0005217468],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.99988544,0.000032162494,0.00001207562,0.000018104245,0.000035040073,0.000017139446],"domain_scores_gemma":[0.99977,0.00007212254,0.000072974086,0.00002120888,0.000027202941,0.000036614427],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.000166334,0.00015735131,0.00017348459,0.0010341958,0.00016522229,0.00048534985,0.000239752,0.00021969767,0.00072604045],"category_scores_gemma":[0.00079050864,0.00021931612,0.00009429837,0.0005903761,0.0004688538,0.00017119259,0.00022947717,0.00028357957,0.00011810319],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.001772448,0.000027975719,0.061377432,0.00016281416,0.000061826526,0.006652371,0.00067975366,0.00053916976,0.91228634,0.0027585658,0.000121253805,0.013559957],"study_design_scores_gemma":[0.00006253402,0.00038900884,0.6188777,0.000045174496,0.00018417093,0.016830519,0.0007756341,0.0013771164,0.3537431,0.003937226,0.003748969,0.000028860712],"about_ca_topic_score_codex":0.0011500907,"about_ca_topic_score_gemma":0.00065542676,"teacher_disagreement_score":0.0011500907,"about_ca_system_score_codex":0.00031779832,"about_ca_system_score_gemma":0.000272014,"threshold_uncertainty_score":0.0024288893},"labels":[],"label_agreement":null},{"id":"W2513703067","doi":"10.1017/s0033291716001598","title":"Maternal prenatal depression is associated with decreased placental expression of the imprinted gene <i>PEG3</i>","year":2016,"lang":"en","type":"article","venue":"Psychological Medicine","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":56,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Douglas Mental Health University Institute","funders":"National Institute of Mental Health; Medical Research Council; Directorate for Biological Sciences; NIHR Imperial Biomedical Research Centre; National Institutes of Health; Imperial College London; National Institute for Health and Care Research; Biotechnology and Biological Sciences Research Council; Genesis Research Trust","keywords":"Genomic imprinting; Human placental lactogen; Pregnancy; Edinburgh Postnatal Depression Scale; Antenatal depression; Placenta; Depression (economics); Obstetrics; Cohort; Offspring; Fetus; Placental lactogen; Endocrinology; Medicine; Internal medicine; Biology; Andrology; Gene expression; Gene; Postpartum depression; Genetics; Diabetes mellitus; DNA methylation; Depressive symptoms","score_opus":0.011479190111584775,"score_gpt":0.2627150293439754,"score_spread":0.2512358392323906,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2513703067","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9993086,0.00018507775,0.000101038044,0.000031907846,0.000002485468,0.000002220412,0.0001401282,0.000004720423,0.00022380149],"genre_scores_gemma":[0.99950457,0.00012474469,0.00010100101,0.00001850384,0.0000024307178,0.000002660989,0.00009634597,0.000001775494,0.00014808841],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9998946,0.00001987317,0.000007903689,0.000033964516,0.00002373522,0.00001995525],"domain_scores_gemma":[0.99944466,0.00007178861,0.0003622965,0.000030418842,0.000034055698,0.00005674025],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00013258425,0.00015549676,0.00012816342,0.00021373038,0.00016476447,0.00028113605,0.00016594335,0.00019723315,0.001650234],"category_scores_gemma":[0.00070092117,0.0001344718,0.000119265234,0.00024948764,0.00021500434,0.000055084492,0.00018760092,0.00025014882,0.000119774],"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":[0.000966997,0.0000285656,0.9655587,0.00004643367,0.00007847083,0.00074763905,0.00019613976,0.000039658276,0.026796727,0.000043465512,0.00025837764,0.005238853],"study_design_scores_gemma":[0.0000051209795,0.000052879303,0.99841094,0.0000045863558,0.000016023121,0.00062931963,0.00003187052,0.000055295346,0.0006921978,0.000010706935,0.00009014919,0.0000010033139],"about_ca_topic_score_codex":0.004811869,"about_ca_topic_score_gemma":0.004930306,"teacher_disagreement_score":0.004811869,"about_ca_system_score_codex":0.00024611878,"about_ca_system_score_gemma":0.00011175811,"threshold_uncertainty_score":0.009567738},"labels":[],"label_agreement":null},{"id":"W2514989011","doi":"10.1016/j.placenta.2016.08.093","title":"DNA methylation-associated repression of MEST/PEG1 expression contributes to the invasion of extravillous trophoblast cells","year":2016,"lang":"en","type":"article","venue":"Placenta","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":50,"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 Natural Science Foundation of China","keywords":"Gene knockdown; DNA methylation; Biology; Decidua; Cell migration; Trophoblast; Cell biology; Bisulfite sequencing; Cancer research; Molecular biology; Matrigel; Placenta; Cell culture; Gene expression; Fetus; Angiogenesis; Gene; Genetics","score_opus":0.009354382557413556,"score_gpt":0.23024272581077976,"score_spread":0.2208883432533662,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2514989011","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9928411,0.0009326917,0.004002004,0.00015162234,0.000014756755,0.000009650933,0.00031949382,0.000090721594,0.001637819],"genre_scores_gemma":[0.99598503,0.00028717247,0.0010048083,0.000019821005,0.0000037771445,0.0000068743857,0.0002541135,0.00001699249,0.002421356],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99990046,0.00001828827,0.000008005738,0.000021527834,0.000028645354,0.00002313305],"domain_scores_gemma":[0.9999027,0.000015846636,0.000030252015,0.000016865328,0.000007163124,0.000027174918],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.000100913865,0.00023608199,0.00012604537,0.0002875962,0.00014597514,0.00032628985,0.00022897385,0.0002397856,0.0017034018],"category_scores_gemma":[0.00018997194,0.00022939056,0.00016989687,0.00013991944,0.00027638944,0.00018413345,0.00031799803,0.00045987102,0.0003215426],"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":[0.000058385962,0.0000037606342,0.0007092139,0.000010362086,0.0000032585108,0.00014077236,0.000014196369,0.00005089227,0.99787366,0.00027175297,0.000023233102,0.00084043795],"study_design_scores_gemma":[0.000008390013,0.000033642053,0.025165303,0.0000034298307,0.000011085322,0.0009356658,0.000048659123,0.0010970973,0.97009933,0.00020542719,0.0023877788,0.0000041109597],"about_ca_topic_score_codex":0.0009698148,"about_ca_topic_score_gemma":0.0011376283,"teacher_disagreement_score":0.0017034018,"about_ca_system_score_codex":0.00033496416,"about_ca_system_score_gemma":0.00021354806,"threshold_uncertainty_score":0.005698502},"labels":[],"label_agreement":null},{"id":"W2515063230","doi":"10.1016/j.placenta.2015.07.303","title":"Transient and placenta-specific imprinting in human development","year":2015,"lang":"en","type":"article","venue":"Placenta","topic":"Genetic Syndromes and Imprinting","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":"Child and Family Research Institute; University of British Columbia","funders":"","keywords":"Imprinting (psychology); Genomic imprinting; Placenta; Biology; Cell biology; Pregnancy; Genetics; Fetus; Gene expression; DNA methylation; Gene","score_opus":0.0282525145561611,"score_gpt":0.2527833168940993,"score_spread":0.22453080233793818,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2515063230","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.6946684,0.25196254,0.027396355,0.0026975395,0.0004901514,0.0000386699,0.0008056867,0.00050543615,0.02143528],"genre_scores_gemma":[0.97316295,0.022624133,0.0016370997,0.000065237364,0.00008744347,0.0000092337705,0.0001316546,0.000019745412,0.002262437],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.99988365,0.00003848954,0.000012102069,0.000026906519,0.000020672387,0.000018139797],"domain_scores_gemma":[0.9998246,0.00005413457,0.000045173187,0.000021342208,0.00001322769,0.000041559095],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00027632646,0.0002180345,0.00023762733,0.00081958214,0.00025201126,0.0006970901,0.00037744967,0.00040723503,0.0007589524],"category_scores_gemma":[0.00041428767,0.00022465487,0.00013362117,0.0005422772,0.00088456884,0.0005137498,0.00035691366,0.0005428055,0.00016594001],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0022385858,0.00011046039,0.03125918,0.0009692508,0.00012345507,0.013959922,0.0010594034,0.0020878157,0.7232374,0.10508318,0.0019579032,0.11791334],"study_design_scores_gemma":[0.00009327414,0.0007608096,0.15506189,0.00018377078,0.00032543237,0.035500977,0.0010818829,0.002307986,0.688615,0.0517482,0.06423552,0.00008527719],"about_ca_topic_score_codex":0.0008147427,"about_ca_topic_score_gemma":0.0005927046,"teacher_disagreement_score":0.00081958214,"about_ca_system_score_codex":0.00048185384,"about_ca_system_score_gemma":0.00044735297,"threshold_uncertainty_score":0.00349617},"labels":[],"label_agreement":null},{"id":"W2520543312","doi":"10.1155/2016/7645938","title":"The Association of Pseudohypoparathyroidism Type Ia with Chiari Malformation Type I: A Coincidence or a Common Link?","year":2016,"lang":"en","type":"article","venue":"Case Reports in Medicine","topic":"Genetic Syndromes and Imprinting","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":"McMaster Children's Hospital; McMaster University","funders":"","keywords":"Medicine; Macrocephaly; GNAS complex locus; Calcinosis cutis; Hydrocephalus; Pediatrics; Pseudohypoparathyroidism; Congenital hypothyroidism; Hyperphosphatemia; Osteodystrophy; Family history; Parathyroid hormone; Internal medicine; Endocrinology; Calcinosis; Surgery; Calcification; Thyroid","score_opus":0.01281899398824794,"score_gpt":0.2843591662796567,"score_spread":0.27154017229140875,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2520543312","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9847527,0.006171631,0.001496387,0.0029180911,0.0002486533,0.00007761017,0.0001585207,0.00011007059,0.004066457],"genre_scores_gemma":[0.99614316,0.0016386245,0.0006720475,0.0003026874,0.00078317,0.0000144476935,0.000068266156,0.000012259961,0.00036534475],"study_design_codex":"case_report","study_design_gemma":"case_report","domain_scores_codex":[0.9992631,0.00009709418,0.0001040754,0.00017939914,0.00009096397,0.00026532696],"domain_scores_gemma":[0.99693763,0.0010654203,0.0010733928,0.0002445731,0.00011294335,0.00056608417],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00038374495,0.0012603423,0.000946598,0.0021836096,0.0012520446,0.0013385032,0.0013541894,0.004065704,0.0035814324],"category_scores_gemma":[0.0043358863,0.00095962116,0.0008101028,0.0017746625,0.0021005375,0.0018161313,0.0013098982,0.0023958897,0.0006333418],"study_design_candidate":"case_report","study_design_consensus":"case_report","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00006458673,0.000032655073,0.042114627,0.00004162059,0.000018593902,0.9547788,0.00018213574,0.00004577907,0.0006336497,0.00026751647,0.0002468702,0.00157324],"study_design_scores_gemma":[0.000009441108,0.000034105055,0.009166755,0.000010942136,0.000021230644,0.9898441,0.00012061498,0.00011737078,0.0002540502,0.000138468,0.00027251267,0.000010393691],"about_ca_topic_score_codex":0.0029029273,"about_ca_topic_score_gemma":0.0016849387,"teacher_disagreement_score":0.004065704,"about_ca_system_score_codex":0.00072392763,"about_ca_system_score_gemma":0.0006207473,"threshold_uncertainty_score":0.01198107},"labels":[],"label_agreement":null},{"id":"W2520927888","doi":"10.1186/s12859-016-1238-8","title":"A haplotype-based normalization technique for the analysis and detection of allele specific expression","year":2016,"lang":"en","type":"article","venue":"BMC Bioinformatics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":10,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Institute of Cancer Research; University of Toronto; Ontario Institute for Cancer Research; Université de Montréal; Centre Hospitalier Universitaire Sainte-Justine","funders":"Medical Research Council; Partenariat Canadien Contre Le Cancer; Fonds Québécois de la Recherche sur la Nature et les Technologies; Ontario Institute for Cancer Research","keywords":"Haplotype; DNA microarray; Normalization (sociology); Allele; Genetics; Computational biology; Biology; Haplotype estimation; Gene expression; Gene","score_opus":0.011896984848092967,"score_gpt":0.22670366014951726,"score_spread":0.2148066753014243,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2520927888","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":[0.012373676,0.00026195557,0.97863173,0.00007419908,0.00016108139,0.00010729822,0.0021225275,0.005241803,0.0010256935],"genre_scores_gemma":[0.058920838,0.00021956331,0.93260866,0.00013348353,0.00008199233,0.000649196,0.0041160095,0.0010970159,0.0021732158],"study_design_codex":"design_other","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9976332,0.0004813216,0.00019664587,0.00085741293,0.0007048159,0.00012663676],"domain_scores_gemma":[0.9969313,0.0011750299,0.00042382343,0.00086547213,0.00053591916,0.000068497095],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0031673983,0.00078482257,0.00077969854,0.0018521193,0.0005951313,0.0009636332,0.0010127935,0.0007590519,0.0067262505],"category_scores_gemma":[0.009303691,0.00049106585,0.0010844975,0.0026748728,0.00054638815,0.0007076805,0.0008065896,0.0019299532,0.0035590017],"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":[0.00047899145,0.00018194133,0.016742287,0.00067103317,0.00062870973,0.00038229194,0.00053415133,0.014200527,0.32432923,0.011361622,0.013978282,0.61651105],"study_design_scores_gemma":[0.00013414522,0.0005837768,0.0795549,0.00014372135,0.00044167793,0.0024390572,0.00022740402,0.3986609,0.37066293,0.028427076,0.11839692,0.00032746897],"about_ca_topic_score_codex":0.0017195647,"about_ca_topic_score_gemma":0.0035752894,"teacher_disagreement_score":0.0067262505,"about_ca_system_score_codex":0.0005957337,"about_ca_system_score_gemma":0.0011291843,"threshold_uncertainty_score":0.022501588},"labels":[],"label_agreement":null},{"id":"W2524086747","doi":"10.1002/uog.15631","title":"EP09.34: Prenatal diagnosis of Prader‐Willi syndrome","year":2015,"lang":"en","type":"article","venue":"Ultrasound in Obstetrics and Gynecology","topic":"Genetic Syndromes and Imprinting","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":"Centre Hospitalier Universitaire de Sherbrooke","funders":"","keywords":"Medicine; Polyhydramnios; Obstetrics; Context (archaeology); Fetus; Prenatal diagnosis; Amniotic fluid index; Amniotic fluid; Pregnancy; Pediatrics; Gynecology","score_opus":0.015170379970124947,"score_gpt":0.2403481506961012,"score_spread":0.22517777072597625,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2524086747","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.93833923,0.0050332453,0.0071784374,0.018010665,0.0019133383,0.00056198554,0.0028484797,0.00055916095,0.025555428],"genre_scores_gemma":[0.98063236,0.0024197719,0.0057090204,0.0015149812,0.0010691802,0.0001654128,0.0007817114,0.00006582817,0.007641619],"study_design_codex":"case_report","study_design_gemma":"not_applicable","domain_scores_codex":[0.99942565,0.00009821785,0.00004170105,0.00016900284,0.0001342013,0.00013129797],"domain_scores_gemma":[0.99918157,0.0003493111,0.00015525603,0.000044354012,0.00006092474,0.00020865063],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00028450275,0.0017474565,0.0008852223,0.0023968278,0.0010367829,0.00044840638,0.0013104728,0.0034989468,0.007661581],"category_scores_gemma":[0.0039206166,0.00057669444,0.00056382146,0.000711449,0.00080702704,0.000767371,0.0010437643,0.0025635299,0.0012411269],"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":[0.00005326903,0.000028915862,0.0043441374,0.000037367732,0.0000057541524,0.98877317,0.000155178,0.00010622776,0.0024398493,0.0005755316,0.0009903075,0.0024903296],"study_design_scores_gemma":[0.000015265481,0.00018724907,0.016980276,0.00005366137,0.000017328388,0.97798616,0.000084615036,0.00033899327,0.0010584014,0.00076078187,0.0024911982,0.000025953175],"about_ca_topic_score_codex":0.002363404,"about_ca_topic_score_gemma":0.0015665017,"teacher_disagreement_score":0.007661581,"about_ca_system_score_codex":0.0005012486,"about_ca_system_score_gemma":0.00061040965,"threshold_uncertainty_score":0.025630534},"labels":[],"label_agreement":null},{"id":"W2526178173","doi":"10.1002/uog.15630","title":"EP09.33: Early prenatal diagnosis of Golabi syndrome","year":2015,"lang":"en","type":"article","venue":"Ultrasound in Obstetrics and Gynecology","topic":"Genetic Syndromes and Imprinting","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 de Montréal; Centre Hospitalier Universitaire Sainte-Justine","funders":"","keywords":"Medicine; Polyhydramnios; Organomegaly; Prenatal diagnosis; Amniotic fluid index; Pediatrics; Failure to thrive; Obstetrics; Amniotic fluid; Fetus; Pregnancy; Gynecology; Pathology; Polyneuropathy","score_opus":0.012948194397463421,"score_gpt":0.23281580499516968,"score_spread":0.21986761059770626,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2526178173","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.8878864,0.007521231,0.010443276,0.019888785,0.0019614308,0.0005627144,0.002675023,0.0007797019,0.06828139],"genre_scores_gemma":[0.9768956,0.0031621826,0.0061792145,0.0018434174,0.0007758091,0.00012640833,0.0007201365,0.0000860832,0.010211181],"study_design_codex":"case_report","study_design_gemma":"case_report","domain_scores_codex":[0.999548,0.00008489559,0.000029308034,0.00008375799,0.00012119261,0.0001328499],"domain_scores_gemma":[0.9993074,0.00028268818,0.00009155478,0.000036522386,0.000083194944,0.00019860108],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00025433893,0.0012147594,0.0007704617,0.0018225949,0.0007818993,0.0005321905,0.00076537614,0.0026424835,0.009953005],"category_scores_gemma":[0.0030484523,0.00035186886,0.00035338942,0.00048544633,0.0005321012,0.0004984473,0.00073055975,0.0016503,0.0014098986],"study_design_candidate":"case_report","study_design_consensus":"case_report","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.000094242,0.00003740467,0.006581816,0.00006862825,0.000008516926,0.97795653,0.00021169012,0.00012667649,0.002977317,0.0010923962,0.003174967,0.0076699215],"study_design_scores_gemma":[0.000018111123,0.00011896492,0.024092508,0.00016164636,0.000017040766,0.9640581,0.0001385413,0.00055157504,0.002434154,0.0012803057,0.007103662,0.000025326384],"about_ca_topic_score_codex":0.0038133094,"about_ca_topic_score_gemma":0.0020318176,"teacher_disagreement_score":0.009953005,"about_ca_system_score_codex":0.00058225257,"about_ca_system_score_gemma":0.0006037174,"threshold_uncertainty_score":0.03329605},"labels":[],"label_agreement":null},{"id":"W2527298399","doi":"10.1101/076794","title":"Genomic analyses for age at menarche identify 389 independent signals and indicate BMI-independent effects of puberty timing on cancer susceptibility","year":2016,"lang":"en","type":"preprint","venue":"bioRxiv (Cold Spring Harbor Laboratory)","topic":"Genetic Syndromes and Imprinting","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":"University Health Network; University of Toronto; Mount Sinai Hospital; Lunenfeld-Tanenbaum Research Institute; Centre for Global Health Research","funders":"","keywords":"Mendelian randomization; Menarche; Biology; Heritability; Population; Prostate cancer; Genetics; Physiology; Endocrinology; Genotype; Oncology; Demography; Gene; Cancer; Medicine; Genetic variants","score_opus":0.03228565572964071,"score_gpt":0.2978485590993267,"score_spread":0.265562903369686,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2527298399","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9888226,0.0008324738,0.003995204,0.00012561788,0.000014528518,0.000006852734,0.0047430056,0.000094543415,0.0013652497],"genre_scores_gemma":[0.9955304,0.000201278,0.0018766657,0.000048040714,0.000010208782,0.0000103047005,0.0015719297,0.000031610907,0.0007195525],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9996841,0.000086285545,0.000017385326,0.00011486928,0.000057444475,0.000039912622],"domain_scores_gemma":[0.99926215,0.00030102982,0.00025703647,0.00008375224,0.00002480329,0.00007124845],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0004577285,0.0003148087,0.00024093282,0.00078523334,0.0002776392,0.00045749772,0.0001962238,0.00021924045,0.004532266],"category_scores_gemma":[0.0009796111,0.0001597012,0.00057709916,0.0007564866,0.00031293608,0.00011270878,0.00035574337,0.00034805833,0.0003490537],"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":[0.0010800908,0.000042954947,0.8735393,0.00009178039,0.0008618969,0.0005837721,0.00018714096,0.0012764321,0.10117413,0.0007417234,0.0007161398,0.01970467],"study_design_scores_gemma":[0.0000145794265,0.000035216544,0.994145,0.000006660888,0.00012238724,0.0002870345,0.000029451729,0.00071331946,0.003576458,0.00020281441,0.00086055876,0.000006509158],"about_ca_topic_score_codex":0.003634565,"about_ca_topic_score_gemma":0.0042652483,"teacher_disagreement_score":0.004532266,"about_ca_system_score_codex":0.00020757313,"about_ca_system_score_gemma":0.00022712868,"threshold_uncertainty_score":0.015161991},"labels":[],"label_agreement":null},{"id":"W2530594373","doi":"10.1182/blood.v112.11.202.202","title":"An Upstream Insulator Element Regulates DLK1 Imprinting in AML","year":2008,"lang":"en","type":"article","venue":"Blood","topic":"Genetic Syndromes and Imprinting","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":"University of Toronto; Princess Margaret Cancer Centre","funders":"","keywords":"Biology; Genomic imprinting; MEG3; CpG site; DNA methylation; Methylation; Imprinting (psychology); Molecular biology; Promoter; Genetics; Cancer research; Gene; Uniparental disomy; Gene expression; Downregulation and upregulation; Long non-coding RNA; Chromosome","score_opus":0.008113948638552441,"score_gpt":0.22598488199235234,"score_spread":0.2178709333537999,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2530594373","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9982168,0.00025860826,0.00060852704,0.000034865898,0.0000060342713,0.000004695038,0.00033052717,0.000043201657,0.0004966677],"genre_scores_gemma":[0.9989955,0.000057985937,0.00027718657,0.00001930224,0.000002597203,0.0000023744956,0.00024851845,0.0000065470767,0.00038996452],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99993575,0.000008578351,0.0000049466303,0.000017222548,0.00001849485,0.00001512725],"domain_scores_gemma":[0.99992514,0.000019024299,0.00002848058,0.0000062237827,0.0000047317485,0.000016313445],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.000051173938,0.00010085845,0.00010200431,0.00022138136,0.0000766822,0.00011379259,0.000082882594,0.00007916521,0.002086541],"category_scores_gemma":[0.0001220656,0.00007551101,0.00011321311,0.0001254889,0.00013179619,0.000044382068,0.00015803262,0.00016263945,0.0002925486],"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":[0.00022818337,0.000013781903,0.0093346415,0.000019718993,0.000007009612,0.000114584946,0.000021121545,0.00007186274,0.9871494,0.00010652618,0.00006836472,0.0028648013],"study_design_scores_gemma":[0.00006952152,0.00035218272,0.39046133,0.000015307605,0.00006704482,0.0017053969,0.00008837713,0.0026790411,0.59862304,0.00040190198,0.0055250325,0.000011744898],"about_ca_topic_score_codex":0.00038504988,"about_ca_topic_score_gemma":0.0007070899,"teacher_disagreement_score":0.002086541,"about_ca_system_score_codex":0.00018855298,"about_ca_system_score_gemma":0.000076434786,"threshold_uncertainty_score":0.0069801807},"labels":[],"label_agreement":null},{"id":"W2538843384","doi":"10.1016/j.molmet.2016.10.004","title":"Targeting the endocannabinoid/CB1 receptor system for treating obesity in Prader–Willi syndrome","year":2016,"lang":"en","type":"article","venue":"Molecular Metabolism","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":74,"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":"Eunice Kennedy Shriver National Institute of Child Health and Human Development; National Institutes of Health; Israel Science Foundation; National Institute for Health and Care Research; Canadian Institutes of Health Research; Foundation for Prader-Willi Research","keywords":"Endocannabinoid system; Cannabinoid receptor; Rimonabant; Medicine; Receptor; Obesity; 2-Arachidonoylglycerol; Internal medicine; Endocrinology; Neuroscience; Pharmacology; Biology; Agonist","score_opus":0.006027089376842569,"score_gpt":0.2170869620226673,"score_spread":0.21105987264582474,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2538843384","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9835565,0.010469743,0.003301189,0.0003508174,0.00007474228,0.00010824755,0.0002115059,0.00014359794,0.0017837118],"genre_scores_gemma":[0.9789433,0.010516734,0.00810907,0.00029040582,0.000038493126,0.00012415853,0.00044279973,0.000019047231,0.001515989],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9999324,0.000012058213,0.000008816771,0.00001310944,0.000019971276,0.000013610941],"domain_scores_gemma":[0.9999654,0.0000036138179,0.000010429838,0.0000033366648,0.0000029019984,0.00001432927],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00018096286,0.0004700558,0.0005306137,0.00036378353,0.00015957013,0.00017061636,0.00032928953,0.00035349905,0.0010327499],"category_scores_gemma":[0.00007303345,0.00017136947,0.00037214495,0.00018720869,0.0003274519,0.00018666593,0.0002684401,0.00096341653,0.00023952305],"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":[0.00090878893,0.0003125935,0.0007946588,0.00017004203,0.000055869466,0.0007060835,0.000040779196,0.00013525615,0.9788012,0.00025200134,0.00026184382,0.017560799],"study_design_scores_gemma":[0.0022919269,0.015346947,0.063529104,0.00016868806,0.0006701813,0.012140318,0.0001777314,0.0035662393,0.876045,0.00047728952,0.025479248,0.000107447915],"about_ca_topic_score_codex":0.00060556957,"about_ca_topic_score_gemma":0.0020894888,"teacher_disagreement_score":0.0010327499,"about_ca_system_score_codex":0.00019937275,"about_ca_system_score_gemma":0.00025562057,"threshold_uncertainty_score":0.003454864},"labels":[],"label_agreement":null},{"id":"W2539027126","doi":"10.1111/pde.13014","title":"Pilomatricoma Associated with Kabuki Syndrome","year":2016,"lang":"en","type":"article","venue":"Pediatric Dermatology","topic":"Genetic Syndromes and Imprinting","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":"Université Laval; Université de Montréal; Centre Hospitalier Universitaire Sainte-Justine","funders":"","keywords":"Pilomatricoma; Medicine; Kabuki; Wnt signaling pathway; Kabuki syndrome; Carcinogenesis; Dermatology; Pathology; Genetics; Internal medicine; Biology; Signal transduction; Cancer; Pediatrics","score_opus":0.006316566195172781,"score_gpt":0.20570764664078797,"score_spread":0.19939108044561518,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2539027126","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9950656,0.00053461577,0.0010959487,0.00009393798,0.000020400803,0.000021395095,0.000048201717,0.000103256825,0.0030166816],"genre_scores_gemma":[0.99936086,0.00009559941,0.00030400878,0.000028383267,0.000013540569,0.000006816149,0.00001977624,0.000007432225,0.00016358431],"study_design_codex":"case_report","study_design_gemma":"case_report","domain_scores_codex":[0.9994618,0.000061123785,0.000050924,0.0000997131,0.00011889451,0.00020753495],"domain_scores_gemma":[0.99872905,0.00035129616,0.00048646473,0.000121830715,0.000062403924,0.00024890422],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00021091623,0.0012853825,0.00047537874,0.0015293668,0.0013291782,0.0009519174,0.00056345377,0.0012555012,0.0017948074],"category_scores_gemma":[0.0024649808,0.0006893352,0.00049039884,0.0013656508,0.0013172306,0.00054117374,0.0011110568,0.000811122,0.0004582738],"study_design_candidate":"case_report","study_design_consensus":"case_report","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00021265287,0.000048624788,0.112590104,0.00008078239,0.000068925794,0.862945,0.0007946849,0.00037602877,0.01612677,0.0008770657,0.00032536619,0.005553986],"study_design_scores_gemma":[0.000021934731,0.00006530135,0.03450673,0.000010464091,0.000051124447,0.9609414,0.00016071433,0.00025144638,0.003080117,0.00026294295,0.00062792125,0.000019972735],"about_ca_topic_score_codex":0.0015717497,"about_ca_topic_score_gemma":0.0019141618,"teacher_disagreement_score":0.0017948074,"about_ca_system_score_codex":0.00049342855,"about_ca_system_score_gemma":0.00046064236,"threshold_uncertainty_score":0.006004274},"labels":[],"label_agreement":null},{"id":"W2539704783","doi":"10.1093/biolreprod/81.s1.266","title":"Investigating the Molecular Effects of Superovulation and Embryo Culture on Genomic Imprinting in a Mouse Model System.","year":2009,"lang":"en","type":"article","venue":"Biology of Reproduction","topic":"Genetic Syndromes and Imprinting","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":"Western University","funders":"","keywords":"Genomic imprinting; Imprinting (psychology); Biology; Epigenetics; DNA methylation; Embryo; Genetics; Embryonic stem cell; Methylation; Embryo culture; Gene; Embryogenesis; Gene expression","score_opus":0.007152254045509899,"score_gpt":0.22713766172061434,"score_spread":0.21998540767510444,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2539704783","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9645653,0.014141614,0.014659739,0.00046867403,0.00025435648,0.00019081768,0.0013779656,0.000236983,0.0041046357],"genre_scores_gemma":[0.95752,0.009723222,0.019867674,0.00030006754,0.00008201434,0.0003158946,0.0014489722,0.00011097726,0.010631107],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9998216,0.000030804935,0.000013483373,0.000050784583,0.000048547063,0.00003484048],"domain_scores_gemma":[0.99977666,0.00006582356,0.00006332454,0.000028544484,0.000020989895,0.000044701424],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00034728687,0.00053271576,0.00027813012,0.00037822337,0.00019968742,0.00023237533,0.00038652704,0.00042046257,0.0013973488],"category_scores_gemma":[0.00016078835,0.00020005771,0.000413593,0.00022404308,0.0003221618,0.0003363108,0.0002454343,0.00074523815,0.00039502594],"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":[0.00008763741,0.0000150210735,0.000084296305,0.000022684302,0.0000039624256,0.00002860482,0.000008791344,0.000017149923,0.998818,0.00003767499,0.000017015394,0.0008591818],"study_design_scores_gemma":[0.000010272738,0.0003915213,0.0032811156,0.0000035760597,0.000024247778,0.00009236766,0.000011864581,0.00019612187,0.99487704,0.000034740293,0.0010729264,0.000004288567],"about_ca_topic_score_codex":0.0007370544,"about_ca_topic_score_gemma":0.0015863223,"teacher_disagreement_score":0.0013973488,"about_ca_system_score_codex":0.00030289774,"about_ca_system_score_gemma":0.00021078676,"threshold_uncertainty_score":0.004674554},"labels":[],"label_agreement":null},{"id":"W2551400455","doi":"10.1186/s13072-016-0104-2","title":"Widespread recovery of methylation at gametic imprints in hypomethylated mouse stem cells following rescue with DNMT3A2","year":2016,"lang":"en","type":"article","venue":"Epigenetics & Chromatin","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":12,"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","funders":"Medical Research Council; Cereal Partners Worldwide; Ulster University","keywords":"Biology; Methylation; DNA methylation; Stem cell; Genetics; Human genetics; Computational biology; Gene; Gene expression","score_opus":0.0101238654089752,"score_gpt":0.2261453435508654,"score_spread":0.2160214781418902,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2551400455","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99126244,0.0007825554,0.0061051724,0.000042355852,0.000018362109,0.00002087053,0.00074361474,0.000114431605,0.00091027596],"genre_scores_gemma":[0.9891957,0.0006354377,0.0036251605,0.00005228666,0.0000070149713,0.000043853528,0.0011620865,0.00007670579,0.005201901],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9998523,0.000014992726,0.00002010742,0.000042450007,0.000049360366,0.000020727664],"domain_scores_gemma":[0.9998167,0.000021755963,0.00005583763,0.000039341572,0.000018827643,0.00004763732],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00018240209,0.00032136822,0.00025087062,0.00025641243,0.00009547726,0.00021136658,0.00026440973,0.00021988334,0.0010925177],"category_scores_gemma":[0.000113053335,0.00020155034,0.00026097152,0.00012156681,0.00024612652,0.00013767958,0.00026185333,0.00073100376,0.00036948465],"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":[0.000011811051,0.0000019050038,0.0001640466,0.000007412365,0.0000025600673,0.00001955289,0.0000104039,0.000015765567,0.9994411,0.000032131462,0.000004184796,0.00028925133],"study_design_scores_gemma":[0.0000037893324,0.000086599124,0.007377772,0.0000033826188,0.00001264093,0.00015967379,0.000020196354,0.00033336767,0.9910034,0.0000570817,0.00093958376,0.0000026184537],"about_ca_topic_score_codex":0.00056050293,"about_ca_topic_score_gemma":0.00088371884,"teacher_disagreement_score":0.0010925177,"about_ca_system_score_codex":0.000116192256,"about_ca_system_score_gemma":0.00016144109,"threshold_uncertainty_score":0.0036548376},"labels":[],"label_agreement":null},{"id":"W2551678515","doi":"10.1055/s-0036-1593840","title":"An Update on Molecular Diagnostic Testing of Human Imprinting Disorders","year":2016,"lang":"en","type":"review","venue":"Journal of Pediatric Genetics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":27,"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; University of Toronto; McMaster University","funders":"","keywords":"Genomic imprinting; Imprinting (psychology); Molecular imprinting; Gene; Biology; Computational biology; Genetics; Bioinformatics; Gene expression; DNA methylation; Biochemistry","score_opus":0.02148006789144498,"score_gpt":0.31226309378601164,"score_spread":0.29078302589456667,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2551678515","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":[0.0001452125,0.99546355,0.0005175462,0.0011002452,0.001082272,0.000005951764,0.000053810825,0.00002477441,0.0016066845],"genre_scores_gemma":[0.0011838098,0.9942272,0.0009119142,0.0011454412,0.0014763075,0.000010457193,0.00013095018,0.0000060646385,0.0009078035],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.9995209,0.000109784036,0.00008358152,0.00006813149,0.00017867678,0.000038940736],"domain_scores_gemma":[0.9984314,0.00093407725,0.00011635899,0.000037157275,0.00038786844,0.00009300457],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0012552704,0.0007864637,0.0013269754,0.0028879782,0.00025092778,0.0010949752,0.0012273934,0.0013905222,0.0049725208],"category_scores_gemma":[0.0026995377,0.00030169476,0.0006149313,0.0016847791,0.0005982082,0.0015239343,0.00066846755,0.0021657527,0.0027366127],"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":[0.00006134077,0.000040911716,0.00055593275,0.0064647496,0.00010914827,0.00089110987,0.000054266246,0.00023183193,0.0015124998,0.0026647823,0.086216204,0.90119725],"study_design_scores_gemma":[0.000019770781,0.00005759168,0.0009788354,0.0036443556,0.00020470316,0.007331188,0.00005469962,0.000095231764,0.000618226,0.0018652312,0.9851053,0.000024821138],"about_ca_topic_score_codex":0.0008318349,"about_ca_topic_score_gemma":0.0016028861,"teacher_disagreement_score":0.0049725208,"about_ca_system_score_codex":0.0007436894,"about_ca_system_score_gemma":0.0010315547,"threshold_uncertainty_score":0.016634703},"labels":[],"label_agreement":null},{"id":"W2558344898","doi":"10.1182/blood.v114.22.379.379","title":"Necdin Regulates Hematopoietic Stem Cell Quiescence and Sensitivity to Genotoxic Stress.","year":2009,"lang":"en","type":"article","venue":"Blood","topic":"Genetic Syndromes and Imprinting","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":"University of Alberta","funders":"","keywords":"Haematopoiesis; Biology; Stem cell; Null cell; Bone marrow; Stromal cell; Transplantation; Myeloid; Cancer research; Cell biology; Immunology; Cell culture; Genetics; Internal medicine; Medicine","score_opus":0.005984711559342947,"score_gpt":0.20369361230941213,"score_spread":0.1977089007500692,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2558344898","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9949138,0.001961581,0.0008434077,0.00007258279,0.000011169394,0.000013988878,0.00048101498,0.00007235783,0.0016300842],"genre_scores_gemma":[0.9962224,0.00050519966,0.00035160346,0.000031077478,0.000002895915,0.000014944793,0.0005668792,0.0000112578255,0.0022938328],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9999026,0.00001610079,0.000009492537,0.000019556193,0.00002628363,0.000025856898],"domain_scores_gemma":[0.9998982,0.000009349393,0.00003772537,0.000010656651,0.000010174719,0.0000339311],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.000066851666,0.00021712254,0.00017153409,0.00024911328,0.000121478384,0.0002489886,0.00017610253,0.00021213622,0.0015446962],"category_scores_gemma":[0.000082545004,0.00010648927,0.00015241986,0.00012714932,0.0001932692,0.00013149843,0.00027507343,0.0003288243,0.0003550847],"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":[0.00012459897,0.000011253256,0.0004087832,0.000020590667,0.0000028969077,0.000053555275,0.000008717681,0.00003093417,0.9980038,0.00007059742,0.00004734939,0.0012170626],"study_design_scores_gemma":[0.000018750174,0.00023267625,0.029157782,0.000009074154,0.000022174772,0.0003325997,0.00005947007,0.0010655118,0.9668775,0.0000759298,0.0021442787,0.000004242041],"about_ca_topic_score_codex":0.0005818911,"about_ca_topic_score_gemma":0.0010320162,"teacher_disagreement_score":0.0015446962,"about_ca_system_score_codex":0.0002972698,"about_ca_system_score_gemma":0.00014190045,"threshold_uncertainty_score":0.0051674843},"labels":[],"label_agreement":null},{"id":"W2559984380","doi":"10.1142/9789813144279_0007","title":"Genetic and Epigenetic Variation at the <i>H19</i> Imprinted Region and Its Effect on Birth Weight","year":2016,"lang":"en","type":"book-chapter","venue":"WORLD SCIENTIFIC eBooks","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","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 Health Centre; McGill University; Jewish General Hospital","funders":"Health Science Center, University of Tennessee; National Institutes of Health; National Institute of Child Health and Human Development; Mitacs","keywords":"Epigenetics; Genomic imprinting; Variation (astronomy); Imprinting (psychology); Biology; Genetics; Evolutionary biology; DNA methylation; Physics; Gene; Astrophysics","score_opus":0.009343419746129364,"score_gpt":0.2054754599127091,"score_spread":0.19613204016657973,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2559984380","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.5439765,0.28444102,0.013662249,0.0063618454,0.0014888942,0.00004901382,0.0036442878,0.00023522571,0.14614105],"genre_scores_gemma":[0.70604974,0.13362557,0.004503346,0.001295269,0.00089133484,0.00005835131,0.001390993,0.0001362576,0.15204906],"study_design_codex":"design_other","study_design_gemma":"observational","domain_scores_codex":[0.99996984,0.0000065146533,0.0000014200428,0.000008080454,0.000010613719,0.0000035403075],"domain_scores_gemma":[0.9999484,0.000034785928,0.0000060609013,0.0000027159563,0.0000026903706,0.000005292667],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00009672926,0.00017966052,0.00010718672,0.00021633603,0.00007599515,0.00020331878,0.00023841755,0.00017386067,0.004187353],"category_scores_gemma":[0.0001672271,0.00011402666,0.00019440195,0.0003064633,0.0001914074,0.00010269179,0.00013981594,0.00034883365,0.00059589447],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0019988187,0.00027341675,0.02787313,0.00045015605,0.00042354802,0.0021719611,0.00050315226,0.002257498,0.29371268,0.018317794,0.015080997,0.6369368],"study_design_scores_gemma":[0.00011528265,0.0013019972,0.67576087,0.00025122837,0.00040779522,0.0057600723,0.0003514127,0.0017049081,0.08282139,0.0407962,0.19061626,0.000112630594],"about_ca_topic_score_codex":0.0014437215,"about_ca_topic_score_gemma":0.0019223484,"teacher_disagreement_score":0.004187353,"about_ca_system_score_codex":0.00015391906,"about_ca_system_score_gemma":0.00008676533,"threshold_uncertainty_score":0.014008045},"labels":[],"label_agreement":null},{"id":"W2560135976","doi":"10.1681/asn.2016010069","title":"Genetic Variants Associated with Circulating Parathyroid Hormone","year":2016,"lang":"en","type":"article","venue":"Journal of the American Society of Nephrology","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":70,"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","funders":"National Center for Research Resources; U.S. National Library of Medicine; National Institute of General Medical Sciences; National Human Genome Research Institute; National Institute of Mental Health; National Heart, Lung, and Blood Institute; National Institute on Aging; National Institutes of Health; Ministry of Cultural Affairs; Roche Diabetes Care; Abbott Diabetes Care; Universitair Medisch Centrum Groningen; Göteborgs Läkaresällskap; Siemens; Vetenskapsrådet; Novo Nordisk; Bundesministerium für Bildung und Forschung; Vrije Universiteit Amsterdam; Stiftelsen för Strategisk Forskning; National Center for Advancing Translational Sciences; Leids Universitair Medisch Centrum; Universiteit Leiden; Insulet Corporation; Nipro; Nederlandse Organisatie voor Wetenschappelijk Onderzoek; Wellcome Trust; National Institute of Arthritis and Musculoskeletal and Skin Diseases; National Institute of Diabetes and Digestive and Kidney Diseases; Sanofi; European Commission; Universität Greifswald; Johns Hopkins University; Eli Lilly and Company; Novo Nordisk Fonden; Foundation for the National Institutes of Health","keywords":"Parathyroid hormone; CYP24A1; Single-nucleotide polymorphism; Internal medicine; Endocrinology; Vitamin D and neurology; Minor allele frequency; Biology; Secondary hyperparathyroidism; SNP; Calcitriol receptor; Medicine; Genotype; Genetics; Calcium; Gene","score_opus":0.009539322404251978,"score_gpt":0.22858521971117188,"score_spread":0.2190458973069199,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2560135976","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9968286,0.00073966925,0.00071110437,0.00012126502,0.000031937085,0.000011949666,0.0009259962,0.000023209568,0.0006061921],"genre_scores_gemma":[0.9986229,0.00013493505,0.00052549446,0.00004878953,0.000028967055,0.000008201291,0.000396696,0.00000837748,0.00022559255],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9989229,0.0001966895,0.0001366092,0.00046319937,0.00017011314,0.00011040502],"domain_scores_gemma":[0.99818546,0.00079990685,0.0005437758,0.00013699586,0.00015953525,0.0001742306],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00071317184,0.00038492127,0.0004769142,0.00062477775,0.00037728134,0.0006405544,0.00035744705,0.0005654182,0.0019810088],"category_scores_gemma":[0.0033592212,0.00016845234,0.0006508981,0.0015843193,0.0003817471,0.00014134584,0.00027622134,0.00046096128,0.0001944648],"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":[0.0011210297,0.000060242426,0.9650375,0.00008600263,0.00096530607,0.0026482388,0.00033361663,0.0005564131,0.01947705,0.0005480223,0.0007760803,0.008390484],"study_design_scores_gemma":[0.000091924994,0.00014120198,0.99338734,0.000018992025,0.00047076482,0.0018391357,0.00006617865,0.000791736,0.0013051709,0.0004734286,0.001395671,0.000018394083],"about_ca_topic_score_codex":0.006534688,"about_ca_topic_score_gemma":0.0051849857,"teacher_disagreement_score":0.006534688,"about_ca_system_score_codex":0.00027215487,"about_ca_system_score_gemma":0.00032136793,"threshold_uncertainty_score":0.012993336},"labels":[],"label_agreement":null},{"id":"W2560187753","doi":"10.1172/jci88648","title":"Deficiency in prohormone convertase PC1 impairs prohormone processing in Prader-Willi syndrome","year":2016,"lang":"en","type":"article","venue":"Journal of Clinical Investigation","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":176,"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 Sherbrooke","funders":"National Institute of Diabetes and Digestive and Kidney Diseases","keywords":"Prohormone convertase; Endocrinology; Prohormone; Internal medicine; Biology; Proinsulin; Knockout mouse; Hormone; Gene; Medicine; Insulin; Genetics","score_opus":0.0408665860268086,"score_gpt":0.3312495679486059,"score_spread":0.2903829819217973,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2560187753","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9979353,0.00030538184,0.00088674424,0.00004676701,0.000021991327,0.000013043939,0.00039538453,0.00005708655,0.00033819515],"genre_scores_gemma":[0.99497104,0.00051350717,0.0012548359,0.000045978624,0.0000071532827,0.000022998687,0.0006353964,0.00003434899,0.0025146538],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99986696,0.000013775132,0.000024702338,0.000036942296,0.00003796492,0.000019595596],"domain_scores_gemma":[0.99983823,0.00002345424,0.000054197815,0.000014005541,0.000006293832,0.00006373073],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00008094047,0.00055454596,0.0002317527,0.00039135135,0.00015823996,0.00025133844,0.00021930067,0.00035781236,0.0022562975],"category_scores_gemma":[0.0001409949,0.0002533592,0.0002780511,0.00012611425,0.00037990752,0.00018034705,0.00029899768,0.0006145551,0.00041330466],"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":[0.00014687242,0.000031678323,0.0003930285,0.000022832231,0.000008891215,0.00020920178,0.000016720707,0.00004619845,0.9982017,0.000042113857,0.000025492627,0.00085517607],"study_design_scores_gemma":[0.00006604288,0.0005524856,0.025754744,0.0000114080785,0.000054107608,0.0021366724,0.000058610935,0.0010650128,0.96820194,0.00007867394,0.0020086428,0.000011646637],"about_ca_topic_score_codex":0.0006694012,"about_ca_topic_score_gemma":0.0013147992,"teacher_disagreement_score":0.0022562975,"about_ca_system_score_codex":0.00018812163,"about_ca_system_score_gemma":0.00017523656,"threshold_uncertainty_score":0.007548094},"labels":[],"label_agreement":null},{"id":"W2573478446","doi":"10.1016/j.metabol.2017.01.020","title":"The use of magnetic resonance imaging to characterize abnormal body composition phenotypes in youth with Prader–Willi syndrome","year":2017,"lang":"en","type":"article","venue":"Metabolism","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":24,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Concordia University; University of Alberta","funders":"Canadian Institutes of Health Research","keywords":"Medicine; Interquartile range; Magnetic resonance imaging; Anthropometry; Adipose tissue; Skeletal muscle; Internal medicine; Nuclear medicine; Radiology","score_opus":0.01666072822338955,"score_gpt":0.22725242028795406,"score_spread":0.21059169206456452,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2573478446","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99746907,0.00064870773,0.00074418663,0.0001120239,0.00001253138,0.000011672469,0.00007173188,0.000027156571,0.000902942],"genre_scores_gemma":[0.9978605,0.0005261934,0.0013624488,0.0000526559,0.000017716044,0.000008100034,0.000047824877,0.000009269693,0.0001152657],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99979156,0.00006062127,0.000031553307,0.000032681553,0.000050249084,0.00003325946],"domain_scores_gemma":[0.9995369,0.00018858064,0.000108028384,0.000025294596,0.00006766732,0.00007355495],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0005622033,0.00050067867,0.00028794573,0.0019300983,0.00021952744,0.0004811415,0.0002725654,0.00046268626,0.00029186995],"category_scores_gemma":[0.002325052,0.0002227228,0.00019619275,0.00039706775,0.0004413728,0.0003269154,0.00036650588,0.00045046458,0.0001312286],"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":[0.00030466853,0.000110245084,0.93447703,0.00002883918,0.0000485647,0.008601583,0.00023584558,0.00033910674,0.04032018,0.00012400401,0.00013121551,0.015278641],"study_design_scores_gemma":[0.000027004622,0.00033549897,0.9472129,0.000032519074,0.0000993609,0.031231256,0.00048474903,0.0025270774,0.01722264,0.00016735034,0.0006428735,0.000016942631],"about_ca_topic_score_codex":0.0017680529,"about_ca_topic_score_gemma":0.0019751517,"teacher_disagreement_score":0.0019300983,"about_ca_system_score_codex":0.0001515483,"about_ca_system_score_gemma":0.00028760938,"threshold_uncertainty_score":0.0035155416},"labels":[],"label_agreement":null},{"id":"W2580576361","doi":"10.1136/archdischild-2016-311298","title":"Longitudinal evaluation of sleep disordered breathing in infants with Prader-Willi syndrome","year":2017,"lang":"en","type":"article","venue":"Archives of Disease in Childhood","topic":"Genetic Syndromes and Imprinting","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":true,"ca_institutions":"Hospital for Sick Children; University of Toronto","funders":"","keywords":"Medicine; Polysomnography; Interquartile range; Pediatrics; Obstructive sleep apnea; Sleep study; Retrospective cohort study; Tonsillectomy; Sleep disordered breathing; Breathing; Internal medicine; Apnea; Surgery; Anesthesia","score_opus":0.013089762812245529,"score_gpt":0.2662526455727095,"score_spread":0.25316288276046395,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2580576361","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.999342,0.00024266886,0.00007964955,0.000018125023,0.0000025960017,0.000009473392,0.00019247722,0.0000034727077,0.00010952974],"genre_scores_gemma":[0.99880743,0.00019976668,0.00023728289,0.000018003366,0.000008516987,0.00001804381,0.0006438832,0.0000015368438,0.000065472275],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9994373,0.0001562969,0.00007454868,0.00011199656,0.00012698211,0.000092873386],"domain_scores_gemma":[0.99742764,0.00035790994,0.0013168209,0.00010023058,0.00040735476,0.0003899333],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0012192607,0.0002711329,0.00031961346,0.00077629846,0.00034503045,0.00039734982,0.00031121905,0.0003790702,0.00041064314],"category_scores_gemma":[0.0038564035,0.00020602903,0.00036733068,0.00044356356,0.00022161557,0.00053203554,0.0004710372,0.0005079214,0.00011727711],"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":[0.00004636632,0.000012731212,0.9989201,0.000004076049,0.0000110702285,0.000124568,0.000044656616,0.000012194846,0.00022361039,0.0000028770717,0.000018966284,0.0005788168],"study_design_scores_gemma":[0.0000034587356,0.00020012149,0.99858814,0.000007031832,0.000009714169,0.00084502547,0.00008162084,0.00008717343,0.00010422175,0.0000035094956,0.00006766598,0.000002361169],"about_ca_topic_score_codex":0.005099809,"about_ca_topic_score_gemma":0.0052809557,"teacher_disagreement_score":0.005099809,"about_ca_system_score_codex":0.00036354986,"about_ca_system_score_gemma":0.0005179284,"threshold_uncertainty_score":0.01014024},"labels":[],"label_agreement":null},{"id":"W2581843842","doi":"10.1016/j.fertnstert.2006.07.506","title":"P-159","year":2006,"lang":"en","type":"article","venue":"Fertility and Sterility","topic":"Genetic Syndromes and Imprinting","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","funders":"","keywords":"Medicine","score_opus":0.008495560238070469,"score_gpt":0.2201083053447275,"score_spread":0.21161274510665704,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2581843842","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":[0.0008862216,0.0034179254,0.001383798,0.004130672,0.010961573,0.00013575777,0.0010468912,0.0005887395,0.9774483],"genre_scores_gemma":[0.0013088033,0.00064932794,0.00030501946,0.0011469158,0.0012301755,0.000036009085,0.0003753842,0.00012779255,0.9948206],"study_design_codex":"not_applicable","study_design_gemma":"not_applicable","domain_scores_codex":[0.999741,0.00003211825,0.000017607606,0.000057448513,0.00012252772,0.000029287368],"domain_scores_gemma":[0.9993387,0.0001575476,0.000033052256,0.00009199913,0.00021095535,0.00016777638],"candidate_categories":["insufficient_payload"],"consensus_categories":[],"category_scores_codex":[0.0005564131,0.00092391047,0.00071721285,0.0013976217,0.0011446434,0.00284755,0.0010948193,0.0019447327,0.6857251],"category_scores_gemma":[0.0015961562,0.00031015745,0.0004860418,0.0010931888,0.0004886872,0.0016975519,0.0013805967,0.0014370573,0.5655277],"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":[0.00009087981,0.00006001647,0.00028391212,0.00022701427,0.000008188783,0.00024714204,0.000065076594,0.00009809944,0.0018740918,0.011652469,0.77923656,0.2061566],"study_design_scores_gemma":[0.000015587158,0.00003852877,0.0006756431,0.00010876265,0.0000030832998,0.00021522994,0.000038719172,0.00007728543,0.0002841488,0.0032339264,0.995304,0.0000051978295],"about_ca_topic_score_codex":0.0014094785,"about_ca_topic_score_gemma":0.0032076964,"teacher_disagreement_score":0.3142749,"about_ca_system_score_codex":0.0006052476,"about_ca_system_score_gemma":0.00052669365,"threshold_uncertainty_score":0},"labels":[],"label_agreement":null},{"id":"W2585315210","doi":"10.1038/gim.2016.220","title":"Molecular diagnosis of PIK3CA-related overgrowth spectrum (PROS) in 162 patients and recommendations for genetic testing","year":2017,"lang":"en","type":"article","venue":"Genetics in Medicine","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":140,"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":"Société Française de Dermatologie et de Pathologie Sexuellement Transmissible; Université de Bourgogne; Agence Nationale de la Recherche","keywords":"Phenotype; Allele; Medicine; Genetic testing; Mutation; Mutant; Genetic heterogeneity; Genetic diagnosis; Allelic heterogeneity; DNA sequencing; Bioinformatics; Genetics; Pathology; Biology; Internal medicine; Gene","score_opus":0.01962944552466315,"score_gpt":0.2875711897181372,"score_spread":0.26794174419347405,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2585315210","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9741979,0.008987702,0.002037629,0.0041832845,0.00013067697,0.00009632016,0.0010455599,0.00006963279,0.009251216],"genre_scores_gemma":[0.98943794,0.004412307,0.003480404,0.00066782016,0.00010418582,0.000046324814,0.00085865974,0.00001780401,0.0009746578],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99961096,0.00006161054,0.00009193981,0.00005419511,0.000110258974,0.0000710388],"domain_scores_gemma":[0.9995316,0.00017245288,0.00007568757,0.000027002963,0.00010221862,0.000091065325],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0007683735,0.00036867522,0.0002274095,0.0017310419,0.0004707158,0.0004356208,0.0004398295,0.0008113899,0.0019201803],"category_scores_gemma":[0.0025065944,0.00026447047,0.000394932,0.00078448356,0.00034760218,0.0005688345,0.00044109943,0.0005451966,0.00045691113],"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":[0.0003699991,0.00009080341,0.9341195,0.000063520136,0.000029889949,0.017999588,0.00024311843,0.00036207857,0.003225451,0.0002646743,0.0029154536,0.04031608],"study_design_scores_gemma":[0.00007598207,0.00023274252,0.8967319,0.0004229836,0.00016752738,0.08622642,0.0018472592,0.0019748316,0.0026420474,0.0012720284,0.008372712,0.0000335568],"about_ca_topic_score_codex":0.0026388727,"about_ca_topic_score_gemma":0.0026497534,"teacher_disagreement_score":0.0026388727,"about_ca_system_score_codex":0.00036556492,"about_ca_system_score_gemma":0.0005729825,"threshold_uncertainty_score":0.006423712},"labels":[],"label_agreement":null},{"id":"W2592165355","doi":"10.1159/000454805","title":"Hormonal and Metabolic Responses to a Single Bout of Resistance Exercise in Prader-Willi Syndrome","year":2017,"lang":"en","type":"article","venue":"Hormone Research in Paediatrics","topic":"Genetic Syndromes and Imprinting","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":"University of Alberta","funders":"U.S. Army","keywords":"Resistance training; Hormone; Metabolic syndrome; Endocrinology; Internal medicine; Insulin resistance; Medicine; Physiology; Obesity","score_opus":0.05309056597284074,"score_gpt":0.33803158660827926,"score_spread":0.2849410206354385,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2592165355","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99980825,0.000041239764,0.000043129756,0.000005490753,0.0000019593351,0.0000041662124,0.000038807473,0.0000021566277,0.000054909815],"genre_scores_gemma":[0.99949336,0.00006500421,0.000164393,0.000012968313,0.000004350179,0.000011886078,0.00012798375,0.0000020570576,0.000117905496],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9998423,0.000037708156,0.000013956052,0.00004734902,0.000032163865,0.000026553531],"domain_scores_gemma":[0.9996606,0.00007813748,0.00012149431,0.000018582992,0.000024822484,0.0000963691],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00019726681,0.00062709185,0.00036740315,0.0003498174,0.00017835904,0.0001768424,0.00018946486,0.00028216318,0.0011642145],"category_scores_gemma":[0.0009574928,0.00019603044,0.00025556478,0.00020307387,0.00030602157,0.000121455465,0.0002971267,0.00048802057,0.00012255076],"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":[0.0031306024,0.00053198874,0.9303035,0.000096313255,0.00014443682,0.0046721725,0.00059571787,0.00033434865,0.04990881,0.000034077682,0.00014031134,0.0101077035],"study_design_scores_gemma":[0.000020997784,0.000763641,0.99558264,0.000004741887,0.000022591359,0.0023055158,0.00012566823,0.00013967471,0.0009416385,0.000010704673,0.00007662263,0.0000056039257],"about_ca_topic_score_codex":0.0019136426,"about_ca_topic_score_gemma":0.0021841002,"teacher_disagreement_score":0.0019136426,"about_ca_system_score_codex":0.00021500312,"about_ca_system_score_gemma":0.0001238738,"threshold_uncertainty_score":0.0038947463},"labels":[],"label_agreement":null},{"id":"W2593243414","doi":"10.3390/ijms18030517","title":"Investigating Autism-Related Symptoms in Children with Prader-Willi Syndrome: A Case Study","year":2017,"lang":"en","type":"article","venue":"International Journal of Molecular Sciences","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":34,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Glenrose Rehabilitation Hospital; University of Alberta","funders":"Canadian Institutes of Health Research; Stollery Children’s Hospital Foundation; Children's Hospital Foundation; University of Alberta; Women and Children's Health Research Institute; Children's Health Research Institute","keywords":"Autism Diagnostic Observation Schedule; Autism spectrum disorder; Autism; Intellectual disability; Vineland Adaptive Behavior Scale; Psychology; Clinical psychology; Rating scale; Observational study; Pediatrics; Pervasive developmental disorder; Social skills; Medicine; Psychiatry; Developmental psychology; Internal medicine","score_opus":0.012001346830556767,"score_gpt":0.2852279803621676,"score_spread":0.27322663353161086,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2593243414","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9985129,0.00033560803,0.00026590057,0.00007485194,0.0000086901955,0.00008114384,0.00005105656,0.000009091644,0.0006607493],"genre_scores_gemma":[0.9983193,0.00056765834,0.0007125149,0.00006849298,0.000024532079,0.000045020817,0.00006300368,0.0000075974153,0.0001918026],"study_design_codex":"case_report","study_design_gemma":"case_report","domain_scores_codex":[0.9989046,0.00019020557,0.0001572683,0.00030653639,0.0002385221,0.0002027897],"domain_scores_gemma":[0.9987012,0.00040466376,0.00036975718,0.000084062405,0.00012246847,0.0003177521],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00075387926,0.0013454548,0.00087083696,0.0024977552,0.0020125983,0.0009459142,0.0010704655,0.0017583065,0.001115774],"category_scores_gemma":[0.0035743266,0.0007760304,0.0008625449,0.0014127507,0.0017798218,0.00091580796,0.001767336,0.0011608242,0.00028417987],"study_design_candidate":"case_report","study_design_consensus":"case_report","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00009899131,0.00033592444,0.4109301,0.000121459154,0.000043326967,0.57470787,0.0057088616,0.00008617715,0.0030821487,0.00013430462,0.00020169301,0.004549219],"study_design_scores_gemma":[0.000016995493,0.00040843483,0.15286197,0.000035922512,0.000048203172,0.8419373,0.0030489105,0.00017250914,0.00078128924,0.000077540986,0.00058491196,0.000025998952],"about_ca_topic_score_codex":0.00598276,"about_ca_topic_score_gemma":0.009086029,"teacher_disagreement_score":0.00598276,"about_ca_system_score_codex":0.0010614439,"about_ca_system_score_gemma":0.000860468,"threshold_uncertainty_score":0.011895895},"labels":[],"label_agreement":null},{"id":"W2595510945","doi":"10.1093/biolreprod/81.s1.142","title":"Characterization of the Mouse Kcnq1ot1 Non-Coding RNA.","year":2009,"lang":"en","type":"article","venue":"Biology of Reproduction","topic":"Genetic Syndromes and Imprinting","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":"Western University","funders":"","keywords":"Genomic imprinting; Biology; Imprinting (psychology); Non-coding RNA; Genetics; Gene; Epigenetics; DNA methylation; Gene silencing; Regulation of gene expression; RNA; Gene expression; Computational biology","score_opus":0.009590569694354392,"score_gpt":0.23234196752874567,"score_spread":0.22275139783439127,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2595510945","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9270314,0.009410536,0.046995074,0.0005587606,0.00017656048,0.00044215156,0.007718489,0.00034248203,0.0073245475],"genre_scores_gemma":[0.89636123,0.006880128,0.048085894,0.0005142062,0.00010377117,0.00054227107,0.029389873,0.00032689894,0.017795771],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9998247,0.000012977424,0.000015623398,0.000053674994,0.00006105379,0.00003202929],"domain_scores_gemma":[0.99939346,0.0000943138,0.00018564503,0.00006113522,0.00010323552,0.00016220826],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00022673595,0.00045981936,0.00019850097,0.000645199,0.00027567177,0.00025118224,0.0003427176,0.00032230344,0.0012372967],"category_scores_gemma":[0.00032894753,0.00021818443,0.00031424197,0.00022957282,0.00025705277,0.0001704258,0.00017780226,0.00046591336,0.0013990792],"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":[0.00002195057,0.000006154361,0.00023844793,0.000041421183,0.000002049368,0.00007339836,0.0000144898295,0.000046590365,0.9975574,0.00011059393,0.000033557335,0.0018539412],"study_design_scores_gemma":[0.000025669578,0.0004077892,0.03405227,0.000046251836,0.00004565487,0.0023320206,0.00005873248,0.001134252,0.9338979,0.00020278372,0.027777418,0.000019188734],"about_ca_topic_score_codex":0.0009782726,"about_ca_topic_score_gemma":0.0025009508,"teacher_disagreement_score":0.0012372967,"about_ca_system_score_codex":0.00035961214,"about_ca_system_score_gemma":0.00042027904,"threshold_uncertainty_score":0.004139185},"labels":[],"label_agreement":null},{"id":"W2597256494","doi":"10.1200/jco.2007.25.18_suppl.21178","title":"A novel case of Silver Russell Syndrome (SRS) and male breast cancer","year":2007,"lang":"en","type":"article","venue":"Journal of Clinical Oncology","topic":"Genetic Syndromes and Imprinting","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":"Windsor Regional Hospital","funders":"","keywords":"Medicine; Breast cancer; Cancer; Biopsy; Oncology; Pathology; Internal medicine","score_opus":0.046802345447217196,"score_gpt":0.40222441366332434,"score_spread":0.35542206821610717,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2597256494","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.978563,0.0029715076,0.0017117148,0.0023452472,0.00030830264,0.000083027844,0.0002773064,0.00021390089,0.01352593],"genre_scores_gemma":[0.9943963,0.0006322204,0.0009978308,0.00053812144,0.00048120378,0.00002569061,0.00010963067,0.000024296278,0.0027946942],"study_design_codex":"case_report","study_design_gemma":"case_report","domain_scores_codex":[0.99937314,0.000074297976,0.000049310605,0.00016312393,0.000110022695,0.00023003899],"domain_scores_gemma":[0.99901175,0.00026941075,0.0002500404,0.00009458487,0.000050245053,0.00032389062],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0002933127,0.0013964063,0.00105509,0.0023687265,0.0016085721,0.0011920228,0.001054389,0.0038988944,0.0044589425],"category_scores_gemma":[0.0019351727,0.0009872811,0.00086731795,0.0011981541,0.0012234342,0.0010403636,0.001506726,0.0015659417,0.0014243135],"study_design_candidate":"case_report","study_design_consensus":"case_report","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.000019365689,0.000014100372,0.003021561,0.000010035861,0.0000054080892,0.9952148,0.000068785586,0.00002400062,0.00049798214,0.00016986112,0.00022800555,0.00072606833],"study_design_scores_gemma":[0.0000066710772,0.000025743377,0.0021806627,0.0000030532049,0.0000045476568,0.99712425,0.00003502509,0.00006430461,0.00013782401,0.000072134055,0.00034223343,0.0000036109152],"about_ca_topic_score_codex":0.0017404965,"about_ca_topic_score_gemma":0.002179127,"teacher_disagreement_score":0.0044589425,"about_ca_system_score_codex":0.0010324229,"about_ca_system_score_gemma":0.0006682784,"threshold_uncertainty_score":0.014916599},"labels":[],"label_agreement":null},{"id":"W2605138257","doi":"10.1093/pch/10.4.221a","title":"Case 2: I don't like your tone","year":2005,"lang":"en","type":"article","venue":"Paediatrics & Child Health","topic":"Genetic Syndromes and Imprinting","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":"SickKids Foundation; Hospital for Sick Children; University of Toronto","funders":"","keywords":"Tone (literature); Medicine; Audiology; Philosophy; Linguistics","score_opus":0.013154947667769023,"score_gpt":0.2805507150368905,"score_spread":0.26739576736912146,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2605138257","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.76141167,0.004750889,0.0073572192,0.087122135,0.0061838655,0.0006059559,0.00066195463,0.00054928096,0.13135692],"genre_scores_gemma":[0.92961645,0.0025486916,0.0043333187,0.01981172,0.0019249902,0.00016893161,0.00022608566,0.00020295277,0.041166842],"study_design_codex":"case_report","study_design_gemma":"case_report","domain_scores_codex":[0.9991411,0.000114579496,0.00004745636,0.00018181665,0.00016198785,0.0003531098],"domain_scores_gemma":[0.9987037,0.00022743926,0.00023572911,0.000072950985,0.00013406292,0.00062613183],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00048362455,0.0017059239,0.0011023801,0.0012526822,0.0041468088,0.0017896548,0.0015186975,0.0053695035,0.009834424],"category_scores_gemma":[0.005378187,0.00051789975,0.001195766,0.0012894548,0.0016468349,0.002093408,0.0018352554,0.0054865833,0.0027823946],"study_design_candidate":"case_report","study_design_consensus":"case_report","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00004076202,0.000108385284,0.004998127,0.00004389677,0.000010987011,0.9833571,0.001297174,0.000072393974,0.0005156912,0.0012733979,0.004918018,0.0033641004],"study_design_scores_gemma":[0.000012130642,0.00005707392,0.0017133472,0.00004195748,0.000009052859,0.99172676,0.0011045889,0.00019377383,0.00014719606,0.0007751382,0.0042019226,0.0000171779],"about_ca_topic_score_codex":0.005723041,"about_ca_topic_score_gemma":0.005395483,"teacher_disagreement_score":0.009834424,"about_ca_system_score_codex":0.0013715514,"about_ca_system_score_gemma":0.0012548747,"threshold_uncertainty_score":0.0328995},"labels":[],"label_agreement":null},{"id":"W2611012165","doi":"10.1016/j.celrep.2017.04.020","title":"Large-Scale Analysis of Loss of Imprinting in Human Pluripotent Stem Cells","year":2017,"lang":"en","type":"article","venue":"Cell Reports","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":104,"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":"Azrieli Foundation; Rosetrees Trust","keywords":"Induced pluripotent stem cell; Imprinting (psychology); Genomic imprinting; Biology; Germline; Embryonic stem cell; DNA methylation; Somatic cell; Genetics; Epigenetics; Stem cell; Gene; Gene expression","score_opus":0.009685806512709946,"score_gpt":0.24803655244467748,"score_spread":0.23835074593196753,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2611012165","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.95569074,0.0015837257,0.035517696,0.000064579835,0.000023160334,0.00007110873,0.0057632276,0.00027509624,0.0010106795],"genre_scores_gemma":[0.9642937,0.0008969661,0.023805726,0.00009794359,0.000012689156,0.0000839056,0.009860401,0.0001226382,0.0008260355],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9998574,0.00001352463,0.000011784247,0.00004147323,0.000062486455,0.000013285661],"domain_scores_gemma":[0.99980026,0.0000717684,0.000038974064,0.000030934396,0.00003525099,0.000022769997],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00028374995,0.00016332699,0.00020037673,0.00044259612,0.00016123525,0.00032168423,0.00012102562,0.00013014706,0.000433598],"category_scores_gemma":[0.00035064513,0.00009212548,0.00022900134,0.0004088643,0.00012974435,0.00010774225,0.00029385937,0.00031074704,0.00023081726],"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":[0.000027843316,0.000007459587,0.003504497,0.000044378183,0.00002537705,0.00005351352,0.000026976324,0.00045637347,0.9906945,0.00007315937,0.00006785845,0.005017914],"study_design_scores_gemma":[0.00000858354,0.00013124791,0.19762598,0.000014489402,0.000108085835,0.0004371423,0.00013309246,0.009540275,0.7852105,0.00048758095,0.0062816534,0.000021273378],"about_ca_topic_score_codex":0.00058531924,"about_ca_topic_score_gemma":0.001211929,"teacher_disagreement_score":0.00058531924,"about_ca_system_score_codex":0.00015350412,"about_ca_system_score_gemma":0.00017601592,"threshold_uncertainty_score":0.0015006065},"labels":[],"label_agreement":null},{"id":"W2612348400","doi":"10.14288/1.0340922","title":"Detailed phenotyping and next-generation sequencing for characterization of rare overgrowth syndromes","year":2017,"lang":"en","type":"article","venue":"Open Collections","topic":"Genetic Syndromes and Imprinting","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":"University of British Columbia","funders":"","keywords":"DNA sequencing; Computer science; Computational biology; Medicine; Biology; Genetics; Gene","score_opus":0.05838203144902022,"score_gpt":0.27657928565151435,"score_spread":0.21819725420249414,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2612348400","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.91051805,0.0013209573,0.07539998,0.0001917967,0.00006164222,0.00035448282,0.008337139,0.00041482723,0.0034011062],"genre_scores_gemma":[0.8875834,0.0014370129,0.09751199,0.00042496415,0.00004805751,0.0004926879,0.010422631,0.0002262562,0.0018531481],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9993338,0.00010993697,0.00007180967,0.00022846129,0.00017794162,0.00007794331],"domain_scores_gemma":[0.9994628,0.00018160499,0.000084585714,0.00007593792,0.0001239138,0.000071200535],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00045339245,0.00061169086,0.00048949354,0.0021415092,0.0002951681,0.00039557953,0.000288052,0.00050220126,0.0010347704],"category_scores_gemma":[0.0013656489,0.00021248824,0.00062288943,0.0007914384,0.00021260639,0.00016769096,0.00045956954,0.00048283933,0.0004270078],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00045250222,0.00011892145,0.15501851,0.0002607814,0.00025306238,0.0090992795,0.0008958199,0.0032742883,0.7560422,0.0012569058,0.0015709935,0.07175669],"study_design_scores_gemma":[0.0001218583,0.00055234577,0.6610276,0.00023337771,0.0005822684,0.02241034,0.00061325205,0.032138918,0.2428474,0.0019028842,0.037472486,0.00009728843],"about_ca_topic_score_codex":0.0022249615,"about_ca_topic_score_gemma":0.0031265316,"teacher_disagreement_score":0.0022249615,"about_ca_system_score_codex":0.00023832027,"about_ca_system_score_gemma":0.0003349319,"threshold_uncertainty_score":0.0044240355},"labels":[],"label_agreement":null},{"id":"W2613710287","doi":"10.5489/cuaj.4297","title":"Recurrent, bilateral, and metastatic pheochromocytoma in a young patient with Beckwith-Wiedemann syndrome: A genetic link?","year":2017,"lang":"en","type":"article","venue":"Canadian Urological Association Journal","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":7,"is_retracted":false,"has_abstract":true,"route_ca_aff":false,"route_ca_fund":false,"route_ca_venue":true,"route_about_ca":false,"ca_institutions":"","funders":"","keywords":"Beckwith–Wiedemann syndrome; Pheochromocytoma; Paraganglioma; Histopathology; Comparative genomic hybridization; Medicine; Pathology; Genotyping; Bioinformatics; Genetics; Biology; Chromosome; Gene; Genotype","score_opus":0.008952839217501106,"score_gpt":0.2179903056821508,"score_spread":0.20903746646464968,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2613710287","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9853483,0.004546238,0.0014263374,0.0026349036,0.00019131532,0.000091541806,0.00017092707,0.00010934481,0.0054810722],"genre_scores_gemma":[0.9959913,0.0014701578,0.00085509446,0.0005048725,0.00032610018,0.0000139280155,0.000050431452,0.000015521564,0.00077253225],"study_design_codex":"case_report","study_design_gemma":"case_report","domain_scores_codex":[0.99976355,0.000018400699,0.000022581306,0.000060826544,0.000048736565,0.00008601714],"domain_scores_gemma":[0.9994722,0.00015195936,0.00011030015,0.000019749565,0.00003094499,0.00021485222],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00014971402,0.0008122919,0.00062645413,0.0010699797,0.0012662334,0.0007441311,0.0005315124,0.0022158825,0.0014643422],"category_scores_gemma":[0.0013907492,0.0004530585,0.00042251253,0.00094081525,0.0009868282,0.000643785,0.0005628475,0.0012278109,0.00027916327],"study_design_candidate":"case_report","study_design_consensus":"case_report","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00001581185,0.00001196147,0.00918601,0.000022213719,0.0000046333166,0.987992,0.00016536347,0.000033894143,0.0010014987,0.00010766247,0.00015844278,0.0013004357],"study_design_scores_gemma":[0.0000044960107,0.000033821823,0.008637307,0.000010741201,0.000010444829,0.99039125,0.000084609615,0.0000932858,0.0003179008,0.000081266524,0.0003249734,0.0000099385725],"about_ca_topic_score_codex":0.011150426,"about_ca_topic_score_gemma":0.017176064,"teacher_disagreement_score":0.011150426,"about_ca_system_score_codex":0.0010557792,"about_ca_system_score_gemma":0.0010952214,"threshold_uncertainty_score":0.02217102},"labels":[],"label_agreement":null},{"id":"W2615109464","doi":"10.1034/j.1399-0004.2001.600302.2.x","title":"Discoveries in Charcot–Marie–Tooth disease, Crohn's disease and Bardet–Biedl syndrome 4","year":2001,"lang":"en","type":"review","venue":"Clinical Genetics","topic":"Genetic Syndromes and Imprinting","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":"Pacific Centre for Reproductive Medicine; University of British Columbia","funders":"","keywords":"Medicine","score_opus":0.05614264677642138,"score_gpt":0.36644885646761083,"score_spread":0.31030620969118944,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2615109464","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":[0.00018946173,0.9965945,0.00025740685,0.00058307115,0.0008361852,0.0000047015005,0.000014645697,0.000011677481,0.00150828],"genre_scores_gemma":[0.000856014,0.99607486,0.0004422346,0.0005358038,0.00067767286,0.000005952773,0.000034571334,0.0000021774556,0.0013706487],"study_design_codex":"design_other","study_design_gemma":"systematic_review","domain_scores_codex":[0.99973863,0.000044040476,0.000040371055,0.000043398646,0.000107074666,0.000026497508],"domain_scores_gemma":[0.9995752,0.00020312372,0.000044750293,0.000014334502,0.00011123269,0.000051305295],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00089313625,0.0011187844,0.0016252007,0.0027912026,0.0003436407,0.0010817146,0.0012493618,0.0018319591,0.002268765],"category_scores_gemma":[0.00120289,0.00034988695,0.00036491416,0.0021462832,0.0007944578,0.001274523,0.0007489014,0.0018341622,0.0016370525],"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":[0.00020330194,0.00008920975,0.00048193513,0.006805925,0.00009874149,0.004285739,0.00008444607,0.00043383238,0.002301451,0.005811199,0.09276523,0.88663894],"study_design_scores_gemma":[0.00005890662,0.000034240402,0.0007475038,0.0012464725,0.0000788302,0.0090315435,0.000055100256,0.000059191174,0.00039648337,0.0017383787,0.98653436,0.000018910157],"about_ca_topic_score_codex":0.001352302,"about_ca_topic_score_gemma":0.0032421907,"teacher_disagreement_score":0.0027912026,"about_ca_system_score_codex":0.00091835373,"about_ca_system_score_gemma":0.0012919804,"threshold_uncertainty_score":0.0075897574},"labels":[],"label_agreement":null},{"id":"W2619988375","doi":"10.1093/molehr/gax029","title":"Intergenerational impact of paternal lifetime exposures to both folic acid deficiency and supplementation on reproductive outcomes and imprinted gene methylation","year":2017,"lang":"en","type":"article","venue":"Molecular Human Reproduction","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":125,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":true,"ca_institutions":"Health Canada; McGill University; William Osler Health System; McGill University Health Centre","funders":"Canadian Institutes of Health Research","keywords":"Biology; Methylation; Folic acid; Folic acid supplementation; Genomic imprinting; DNA methylation; Endocrinology; Genetics; Imprinting (psychology); Gene; Internal medicine; Pregnancy; Gene expression","score_opus":0.016662114616363265,"score_gpt":0.31959485427291484,"score_spread":0.3029327396565516,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2619988375","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9981982,0.00075823517,0.00026304458,0.00007186213,0.000008768996,0.0000073669175,0.00034950985,0.0000059352164,0.00033697332],"genre_scores_gemma":[0.99628925,0.00096258346,0.0004922325,0.00006409195,0.0000066003367,0.000022000222,0.0004562105,0.000004715299,0.001702333],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9998982,0.000021208607,0.0000058446612,0.000035842826,0.000021062513,0.000017845085],"domain_scores_gemma":[0.9997675,0.000036457262,0.00008910662,0.000024798705,0.000020413572,0.000061739614],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00024134482,0.00017710126,0.00023836504,0.00016544756,0.00013311389,0.00019505997,0.00014441703,0.00022412493,0.0012632927],"category_scores_gemma":[0.00021686741,0.00011075239,0.00015011469,0.000098753866,0.00016563745,0.00013492546,0.00021365988,0.00026751522,0.000089933164],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0067651845,0.00048148,0.27131614,0.0002050656,0.00037954983,0.00054767093,0.00031517472,0.00021067889,0.69192135,0.0002993704,0.00038513623,0.02717309],"study_design_scores_gemma":[0.000049804083,0.004355436,0.9347026,0.00003491705,0.00030239133,0.0008652143,0.00027735313,0.0003590065,0.05709869,0.00020369918,0.0017344526,0.000016475771],"about_ca_topic_score_codex":0.001290665,"about_ca_topic_score_gemma":0.0030964245,"teacher_disagreement_score":0.001290665,"about_ca_system_score_codex":0.00020288248,"about_ca_system_score_gemma":0.0002302124,"threshold_uncertainty_score":0.004226148},"labels":[],"label_agreement":null},{"id":"W2624029039","doi":"10.1096/fj.201700229r","title":"<i>In vivo</i> imaging of prodromal hippocampus CA1 subfield oxidative stress in models of Alzheimer disease and Angelman syndrome","year":2017,"lang":"en","type":"article","venue":"The FASEB Journal","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":36,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Kingston Health Sciences Centre; Queen's University","funders":"National Eye Institute; National Institute on Aging; Research to Prevent Blindness","keywords":"Oxidative stress; Angelman syndrome; Hippocampus; Disease; Neuroscience; In vivo; Medicine; Pathology; Biology; Internal medicine; Biochemistry; Genetics","score_opus":0.01481228296134809,"score_gpt":0.2531388628538565,"score_spread":0.2383265798925084,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2624029039","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.94879204,0.0033610226,0.03643427,0.000945775,0.000148106,0.00016374043,0.0012379589,0.00084270886,0.008074431],"genre_scores_gemma":[0.9564846,0.0018747364,0.03229217,0.00029077457,0.000026624319,0.00019002818,0.000837952,0.0001327914,0.007870389],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99994075,0.000012692853,0.0000059604577,0.000014220338,0.000012849272,0.00001352964],"domain_scores_gemma":[0.999863,0.00002333352,0.00004239411,0.000013972614,0.00003059307,0.000026551092],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0004015614,0.0004387627,0.00015573596,0.00040455954,0.00017290031,0.00025706575,0.0003034842,0.0005199946,0.0015852132],"category_scores_gemma":[0.00022892734,0.0002142525,0.00014142996,0.00015524268,0.0003276574,0.00037691605,0.00022012857,0.00049961096,0.00025140864],"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":[0.0001863507,0.000027874143,0.00016567043,0.00005670831,0.0000062834256,0.00008151385,0.000019635601,0.00013392341,0.9976616,0.0001937652,0.00026864387,0.0011980053],"study_design_scores_gemma":[0.000050979903,0.00067324284,0.0046418617,0.000020239879,0.000039571863,0.00095202227,0.000055681518,0.0023576498,0.98813474,0.0002522395,0.002808028,0.0000137369625],"about_ca_topic_score_codex":0.0017431082,"about_ca_topic_score_gemma":0.0021611606,"teacher_disagreement_score":0.0017431082,"about_ca_system_score_codex":0.00031501826,"about_ca_system_score_gemma":0.00024236937,"threshold_uncertainty_score":0.005303085},"labels":[],"label_agreement":null},{"id":"W2629299361","doi":"10.1007/s00439-017-1824-5","title":"Analysis of case-parent trios for imprinting effect using a loglinear model with adjustment for sex-of-parent-specific transmission ratio distortion","year":2017,"lang":"en","type":"article","venue":"Human Genetics","topic":"Genetic Syndromes and Imprinting","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":"HEC Montréal; McGill University","funders":"","keywords":"Biology; Imprinting (psychology); Allele; Genetics; Genomic imprinting; Genetic model; Gene; Gene expression","score_opus":0.05227242962283838,"score_gpt":0.3248412895296295,"score_spread":0.2725688599067911,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2629299361","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.7604681,0.0007802311,0.22697558,0.0005624974,0.00023479015,0.00087481894,0.0067924852,0.0014882063,0.0018232929],"genre_scores_gemma":[0.92453814,0.00023255852,0.058753327,0.00016011951,0.000057860856,0.0019046705,0.0049206004,0.00075780373,0.008674975],"study_design_codex":"observational","study_design_gemma":"simulation_or_modeling","domain_scores_codex":[0.94483745,0.04170392,0.0022158136,0.0072236224,0.002043424,0.0019757985],"domain_scores_gemma":[0.9029294,0.07705621,0.003922664,0.013370934,0.0015516591,0.0011690779],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.045617636,0.0023322492,0.0045948187,0.0036215081,0.0017040654,0.002307909,0.007350863,0.002471672,0.021304267],"category_scores_gemma":[0.060652167,0.0014911487,0.007597768,0.0041980715,0.0015825537,0.0024011973,0.0020452207,0.004210157,0.002223681],"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":[0.031003602,0.0036034747,0.68830585,0.0012241595,0.03054809,0.011794264,0.0054060994,0.04978748,0.026799683,0.023364836,0.008795751,0.11936667],"study_design_scores_gemma":[0.0017640612,0.004812932,0.37019926,0.0002987789,0.013071575,0.0074269683,0.0028427406,0.5644905,0.008146254,0.014146306,0.012369163,0.00043147145],"about_ca_topic_score_codex":0.018274985,"about_ca_topic_score_gemma":0.011313514,"teacher_disagreement_score":0.045617636,"about_ca_system_score_codex":0.001714174,"about_ca_system_score_gemma":0.0033231857,"threshold_uncertainty_score":0.241252},"labels":[],"label_agreement":null},{"id":"W2724568932","doi":"10.5038/2074-1235.41.2.1026","title":"Hybridization from Possible Sexual Mis-imprinting: Molecular Characterization of Hybridization Between Brown Sula Leucogaster and Blue-footed Boobies S Nebouxii","year":2013,"lang":"en","type":"article","venue":"Marine ornithology","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":1,"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":"Natural Sciences and Engineering Research Council of Canada; McGill University","keywords":"Ornithology; Imprinting (psychology); Seabird; Biology; Zoology; Genetics; Ecology; Gene; Southern Hemisphere","score_opus":0.007862932673764039,"score_gpt":0.21035160640327727,"score_spread":0.20248867372951324,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2724568932","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9996444,0.000028196717,0.00010771573,0.0000048324123,7.396714e-7,0.0000018291355,0.00003144608,0.0000017120702,0.00017907623],"genre_scores_gemma":[0.99934,0.000029589206,0.00030949677,0.000013112536,0.0000013547086,0.0000049227,0.00012586037,0.0000018236153,0.00017393228],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99994123,0.000008907864,0.0000041872813,0.000022100183,0.000010149301,0.000013410985],"domain_scores_gemma":[0.99980515,0.00004439782,0.000066704844,0.000013643284,0.000016868249,0.000053206197],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.000079414735,0.00013382915,0.00009281229,0.00047179955,0.00017555834,0.00015755881,0.0001257871,0.00020205101,0.00084487576],"category_scores_gemma":[0.00022599286,0.000092525006,0.00010003099,0.00020330811,0.00025272637,0.00007466879,0.00017515253,0.00015076365,0.00014279767],"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":[0.00017617249,0.000030877025,0.1193529,0.000031689447,0.000020493364,0.00028686877,0.0003420196,0.000036622816,0.87671125,0.00006659427,0.000018333309,0.0029261464],"study_design_scores_gemma":[0.0000067335727,0.00016059588,0.97283065,0.000004619402,0.000021500731,0.00089550734,0.00034103103,0.0002599554,0.025070967,0.00004181076,0.0003618884,0.000004560284],"about_ca_topic_score_codex":0.0011846692,"about_ca_topic_score_gemma":0.0030629842,"teacher_disagreement_score":0.0011846692,"about_ca_system_score_codex":0.000102907936,"about_ca_system_score_gemma":0.00007200081,"threshold_uncertainty_score":0.002826333},"labels":[],"label_agreement":null},{"id":"W2734652700","doi":"10.1038/ejhg.2017.102","title":"Wilms tumour in Beckwith–Wiedemann Syndrome and loss of methylation at imprinting centre 2: revisiting tumour surveillance guidelines","year":2017,"lang":"en","type":"article","venue":"European Journal of Human Genetics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":39,"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":"Beckwith–Wiedemann syndrome; Methylation; Wilms' tumor; Wilms tumour; Imprinting (psychology); Uniparental disomy; Genomic imprinting; Medicine; DNA methylation; Oncology; Biology; Internal medicine; Karyotype; Cancer research; Genetics; Chromosome; Gene","score_opus":0.026596188275592715,"score_gpt":0.2868495838775544,"score_spread":0.26025339560196165,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2734652700","genre_codex":"commentary","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":[0.06507852,0.3048617,0.036751185,0.5330134,0.016239025,0.00033199726,0.0013214236,0.001331239,0.041071564],"genre_scores_gemma":[0.5250987,0.18603678,0.099494964,0.13263205,0.035549488,0.0008079452,0.003560194,0.0007159042,0.016104067],"study_design_codex":"design_other","study_design_gemma":"theoretical_or_conceptual","domain_scores_codex":[0.99741757,0.0006509122,0.0009895917,0.0002343512,0.00047165976,0.0002358417],"domain_scores_gemma":[0.9890732,0.0061501265,0.0008666942,0.00036550904,0.0025397525,0.001004674],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.004822766,0.0006672461,0.0012115886,0.0026370739,0.0009755233,0.0015569873,0.0024808627,0.0054454077,0.0009126568],"category_scores_gemma":[0.013405243,0.0005046822,0.0013175557,0.0011198017,0.0014580125,0.001809509,0.0012072455,0.008376654,0.00070300867],"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":[0.00065669423,0.00033074868,0.07286524,0.0025424259,0.0003262407,0.02188683,0.002022859,0.0058648135,0.008021113,0.01640385,0.3321526,0.53692657],"study_design_scores_gemma":[0.00033251377,0.0006624452,0.08330983,0.0153092835,0.001341895,0.09178246,0.0032561233,0.01069391,0.008185503,0.029130528,0.7556541,0.00034140804],"about_ca_topic_score_codex":0.0084730005,"about_ca_topic_score_gemma":0.013030262,"teacher_disagreement_score":0.0084730005,"about_ca_system_score_codex":0.0015919063,"about_ca_system_score_gemma":0.0033789899,"threshold_uncertainty_score":0.025505483},"labels":[],"label_agreement":null},{"id":"W2738352505","doi":"10.1080/17476348.2017.1355241","title":"<i>DLK1-DIO3</i>imprinted locus deregulation in development, respiratory disease, and cancer","year":2017,"lang":"en","type":"review","venue":"Expert Review of Respiratory Medicine","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":30,"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":"Canadian Institutes of Health Research","keywords":"Medicine; Internal medicine; Locus (genetics); Oncology; Intensive care medicine; Genetics; Gene; Biology","score_opus":0.08602050507173746,"score_gpt":0.4124554655017475,"score_spread":0.32643496043001,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2738352505","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":[0.0004750493,0.74045724,0.00091050117,0.19896519,0.04924244,0.000034276367,0.0003680596,0.00015269453,0.009394565],"genre_scores_gemma":[0.0060461494,0.7647848,0.00091536145,0.1424211,0.064850785,0.00006882166,0.000517947,0.00005420762,0.02034078],"study_design_codex":"not_applicable","study_design_gemma":"not_applicable","domain_scores_codex":[0.9992729,0.00023050253,0.00006456455,0.00011111752,0.00025050036,0.00007043761],"domain_scores_gemma":[0.99753726,0.0011844697,0.00023162132,0.00004766984,0.00081203785,0.00018690964],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0014705242,0.00062070147,0.0011303853,0.00069078896,0.00038273825,0.0010435003,0.0015072785,0.0042794235,0.009262752],"category_scores_gemma":[0.0037068883,0.00020650201,0.0008225008,0.0005384784,0.0009975976,0.0010776822,0.0007637831,0.0053339656,0.0041548763],"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":[0.000111480935,0.000011607276,0.00025288403,0.0032271228,0.000081386905,0.0005519109,0.000060779108,0.00016180966,0.0010870832,0.0035514184,0.805396,0.18550651],"study_design_scores_gemma":[0.000038722043,0.000050688355,0.00068806467,0.002415409,0.000061351864,0.0013093741,0.000052909854,0.000093773015,0.00031977784,0.0032275175,0.99172324,0.00001913755],"about_ca_topic_score_codex":0.0018619656,"about_ca_topic_score_gemma":0.004734117,"teacher_disagreement_score":0.009262752,"about_ca_system_score_codex":0.0015363664,"about_ca_system_score_gemma":0.0015166461,"threshold_uncertainty_score":0.030986965},"labels":[],"label_agreement":null},{"id":"W2743543325","doi":"10.1038/gim.2017.105","title":"Genetic disruption of the oncogenic HMGA2–PLAG1–IGF2 pathway causes fetal growth restriction","year":2017,"lang":"en","type":"article","venue":"Genetics in Medicine","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":137,"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":"Université Pierre et Marie Curie; Institut National de la Santé et de la Recherche Médicale; European Commission; Rare Disease Foundation; Agence Nationale de la Recherche; Children’s Hospital of Wisconsin Research Institute; Seattle Children's Research Institute","keywords":"HMGA2; Fetal growth; Genetics; Biology; Genomic imprinting; CRISPR; Intrauterine growth restriction; Fetus; Cancer research; Medicine; Gene; DNA methylation; Pregnancy; microRNA; Gene expression","score_opus":0.01962991651978447,"score_gpt":0.28069400855638804,"score_spread":0.2610640920366036,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2743543325","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9952858,0.0006294563,0.0026507482,0.000071217626,0.000008782639,0.000008949714,0.00018133598,0.000111301204,0.0010523564],"genre_scores_gemma":[0.99809235,0.00028469085,0.0010493312,0.000017574685,0.0000040361947,0.0000055026994,0.00009174237,0.000011857301,0.00044295582],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9999112,0.000018467481,0.000006846007,0.000023023209,0.000025570502,0.000014851185],"domain_scores_gemma":[0.9999155,0.000024821638,0.00003340416,0.000006885716,0.0000033415295,0.000016036498],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00009508557,0.0004183418,0.0001506846,0.0003377285,0.00015675544,0.0000998623,0.0001275363,0.00018638281,0.0019128324],"category_scores_gemma":[0.00017486284,0.00010241327,0.0001413724,0.00014272088,0.0003853969,0.00006892477,0.00027540172,0.00021077952,0.0002390998],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00030340208,0.00003230781,0.040776815,0.00010466553,0.00008256858,0.019050699,0.00012634214,0.00045964157,0.92108583,0.0009686799,0.00034422215,0.016664905],"study_design_scores_gemma":[0.00010246097,0.0004832956,0.22697707,0.000042004445,0.00019624003,0.1621039,0.00029035495,0.0031580434,0.5954014,0.0012853317,0.00993596,0.000023820287],"about_ca_topic_score_codex":0.000444727,"about_ca_topic_score_gemma":0.000984459,"teacher_disagreement_score":0.0019128324,"about_ca_system_score_codex":0.00014452574,"about_ca_system_score_gemma":0.00015192913,"threshold_uncertainty_score":0.0063990355},"labels":[],"label_agreement":null},{"id":"W2743664205","doi":"10.1016/j.jmoldx.2017.07.002","title":"Clinical Validation of a Genome-Wide DNA Methylation Assay for Molecular Diagnosis of Imprinting Disorders","year":2017,"lang":"en","type":"article","venue":"Journal of Molecular Diagnostics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":50,"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; London Health Sciences Centre; Western University","funders":"","keywords":"DNA methylation; Imprinting (psychology); Genomic imprinting; Biology; Genetics; Genome; Methylation; Computational biology; DNA; Gene; Gene expression","score_opus":0.01812132853283012,"score_gpt":0.3117323569973819,"score_spread":0.2936110284645518,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2743664205","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.97361124,0.0028173216,0.0147809945,0.0013885824,0.00019830359,0.0001710769,0.0013839466,0.00034499785,0.00530351],"genre_scores_gemma":[0.99488175,0.00017727328,0.0035467609,0.00026790833,0.00003144705,0.00005358754,0.00049139606,0.000023259803,0.000526526],"study_design_codex":"observational","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99730045,0.000836369,0.00018263859,0.00065954565,0.0008487001,0.0001723067],"domain_scores_gemma":[0.9968334,0.001627661,0.0002592759,0.00030485558,0.0006926333,0.00028217287],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0027096546,0.00062515895,0.0004883666,0.0013395426,0.00040544063,0.0008980698,0.0007075297,0.0013849172,0.0011181457],"category_scores_gemma":[0.008698168,0.00029727662,0.0002731372,0.0004405811,0.0007333114,0.0003472238,0.00047608072,0.0008215166,0.00066150766],"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":[0.0014935881,0.00026477725,0.6426472,0.00014325924,0.00021742296,0.0021333082,0.0004463059,0.0014338042,0.29692224,0.00093184353,0.0018752515,0.051490974],"study_design_scores_gemma":[0.00023287443,0.0028320784,0.71718043,0.00009825811,0.00044038452,0.020555245,0.00048821073,0.023682067,0.22005296,0.0016908563,0.01268212,0.00006461462],"about_ca_topic_score_codex":0.0010063138,"about_ca_topic_score_gemma":0.0009451376,"teacher_disagreement_score":0.0027096546,"about_ca_system_score_codex":0.00044180956,"about_ca_system_score_gemma":0.000592125,"threshold_uncertainty_score":0.014330208},"labels":[],"label_agreement":null},{"id":"W2751630511","doi":"10.1111/gbb.12422","title":"Dopaminergic and behavioural changes in a loss‐of‐imprinting model of <i>Cdkn1c</i>","year":2017,"lang":"en","type":"article","venue":"Genes Brain & Behavior","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":31,"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; Medical Research Council Canada; Wellcome Trust","keywords":"Imprinting (psychology); Dopaminergic; Neuroscience; Psychology; Biology; Dopamine; Genetics","score_opus":0.029026630276423243,"score_gpt":0.27406393081868946,"score_spread":0.24503730054226622,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2751630511","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99491876,0.00034601177,0.0014873736,0.0003171049,0.00009288194,0.000062971376,0.0012425209,0.00021857243,0.0013137321],"genre_scores_gemma":[0.98586744,0.00052859454,0.0021353147,0.00022230022,0.00003698942,0.00017961863,0.0014015306,0.00015662955,0.009471566],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9995883,0.00004342035,0.00004682429,0.00013019245,0.000093906994,0.00009733534],"domain_scores_gemma":[0.9993137,0.000079260404,0.0002181565,0.000054795993,0.000029439952,0.00030463582],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00022149515,0.0010568827,0.00047094154,0.0009896598,0.00039000946,0.0005239574,0.0006504395,0.001048783,0.0030467354],"category_scores_gemma":[0.00021092407,0.00036302328,0.00055022,0.00026874917,0.0010011132,0.00036780004,0.0003648265,0.0021611021,0.00063575635],"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":[0.00064480276,0.00045979102,0.0003596021,0.000028717377,0.000020648302,0.00037149424,0.000044085686,0.00022443669,0.99629396,0.00036444337,0.00018308507,0.0010048484],"study_design_scores_gemma":[0.00026137294,0.004258624,0.013855802,0.000030826952,0.00008794119,0.0015538863,0.00018252204,0.004659855,0.97103566,0.00032716518,0.0036952116,0.000051054252],"about_ca_topic_score_codex":0.0029525526,"about_ca_topic_score_gemma":0.0038681652,"teacher_disagreement_score":0.0030467354,"about_ca_system_score_codex":0.0009920672,"about_ca_system_score_gemma":0.0004863968,"threshold_uncertainty_score":0.010192275},"labels":[],"label_agreement":null},{"id":"W2754709583","doi":"10.1002/uog.18555","title":"EP14.39: Should we consider prenatal diagnosis of Silver–Russell syndrome?","year":2017,"lang":"en","type":"article","venue":"Ultrasound in Obstetrics and Gynecology","topic":"Genetic Syndromes and Imprinting","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 de Montréal; Centre Hospitalier Universitaire Sainte-Justine","funders":"","keywords":"Medicine; Intrauterine growth restriction; Amniocentesis; Pediatrics; Gestational age; Birth weight; Short stature; Failure to thrive; Prenatal diagnosis; Obstetrics; Amniotic fluid; Abdomen; Small for gestational age; Achondroplasia; Fetus; Pregnancy; Surgery","score_opus":0.022237382162049894,"score_gpt":0.26910150174397557,"score_spread":0.24686411958192567,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2754709583","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":[0.28540277,0.06820567,0.021972056,0.5566926,0.019613953,0.0006487063,0.0012259126,0.0010101816,0.04522806],"genre_scores_gemma":[0.7192294,0.06398816,0.03140951,0.11868356,0.046057064,0.0004433239,0.0014258643,0.00038764055,0.018375387],"study_design_codex":"case_report","study_design_gemma":"not_applicable","domain_scores_codex":[0.999137,0.0001742758,0.00013344272,0.00015835205,0.00020326639,0.00019373372],"domain_scores_gemma":[0.997919,0.00086561975,0.00017123848,0.00010418907,0.00043336189,0.00050662865],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00094083545,0.0011546875,0.0013680904,0.0016537698,0.0012054065,0.0012875434,0.0015065768,0.008204303,0.0047423495],"category_scores_gemma":[0.008821301,0.0004465156,0.0007864082,0.00056195393,0.00095762376,0.0028312127,0.00077180273,0.0056292913,0.001664776],"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":[0.00033363097,0.00012874512,0.039371707,0.00036354232,0.00005510734,0.8477507,0.00033274828,0.00048569648,0.0020752852,0.002351558,0.0453182,0.061433],"study_design_scores_gemma":[0.0000810521,0.00019051434,0.01611692,0.001354585,0.0001032995,0.91805726,0.0014645146,0.0015993781,0.0012092189,0.010236244,0.049489986,0.00009705728],"about_ca_topic_score_codex":0.0037319276,"about_ca_topic_score_gemma":0.002650386,"teacher_disagreement_score":0.008204303,"about_ca_system_score_codex":0.00072231545,"about_ca_system_score_gemma":0.0011977627,"threshold_uncertainty_score":0.01586473},"labels":[],"label_agreement":null},{"id":"W2762704796","doi":"10.1093/eep/dvx015","title":"Maintenance of Mest imprinted methylation in blastocyst-stage mouse embryos is less stable than other imprinted loci following superovulation or embryo culture","year":2017,"lang":"en","type":"review","venue":"Current Zoology","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":45,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Children’s Health Research Institute; Western University","funders":"","keywords":"Genomic imprinting; Methylation; Blastocyst; Biology; Imprinting (psychology); DNA methylation; Andrology; Embryo; Insulin-like growth factor 2 receptor; Epigenetics; Embryo culture; Genetics; Embryogenesis; Gene; Growth factor; Gene expression; Medicine","score_opus":0.08081879887219379,"score_gpt":0.36886258394210114,"score_spread":0.28804378506990735,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2762704796","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":[0.00018453671,0.9978859,0.00020776551,0.00024707732,0.00020509212,0.000002947898,0.00003610382,0.000011901938,0.0012187079],"genre_scores_gemma":[0.00091343216,0.99768734,0.00019088546,0.00014576357,0.000113477705,0.0000047711515,0.00005367561,0.000002975304,0.000887622],"study_design_codex":"design_other","study_design_gemma":"observational","domain_scores_codex":[0.99989223,0.000012859816,0.000017940964,0.000020839965,0.00004560353,0.000010436427],"domain_scores_gemma":[0.9997676,0.000101017766,0.000043112006,0.000009535731,0.000053751988,0.000024955432],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00050043175,0.0005342906,0.0008041338,0.0011924322,0.00014852955,0.00062961306,0.0007914964,0.0006159789,0.0024798526],"category_scores_gemma":[0.00047834855,0.00018593355,0.00022045433,0.0011572845,0.0003960236,0.0007710107,0.00044915828,0.0010847962,0.0019324044],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.000068200105,0.00001822125,0.00019674297,0.010333167,0.000056394794,0.000157672,0.00002561419,0.0001870324,0.0048565073,0.003106357,0.01990047,0.96109366],"study_design_scores_gemma":[0.000008509353,0.00004425746,0.00085756637,0.0010924143,0.000070571296,0.0010125496,0.000026286802,0.00003935154,0.0020401191,0.0011689063,0.9936255,0.000013952336],"about_ca_topic_score_codex":0.00052877265,"about_ca_topic_score_gemma":0.0012870003,"teacher_disagreement_score":0.0024798526,"about_ca_system_score_codex":0.00040088117,"about_ca_system_score_gemma":0.00062891556,"threshold_uncertainty_score":0.008295953},"labels":[],"label_agreement":null},{"id":"W2768805139","doi":"10.1098/rsbl.2017.0643","title":"Associations between imprinted gene expression in the placenta, human fetal growth and preeclampsia","year":2017,"lang":"en","type":"article","venue":"Biology Letters","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","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":"University of Toronto; Simon Fraser University","funders":"","keywords":"Genomic imprinting; Imprinting (psychology); Biology; Gene; Placenta; Preeclampsia; Genetics; Microarray; Fetus; Microarray analysis techniques; Gene expression; Gene expression profiling; Pregnancy; DNA methylation","score_opus":0.017628612096924578,"score_gpt":0.2753254026786517,"score_spread":0.2576967905817271,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2768805139","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9976955,0.0011112188,0.0003397125,0.00009912377,0.000005592026,0.000002067324,0.00018024592,0.00001137181,0.000555035],"genre_scores_gemma":[0.99917954,0.00040254602,0.00015951575,0.000014086394,0.00000782932,0.0000022005656,0.000082164224,0.0000028347565,0.00014922114],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9998355,0.000044530283,0.00001592143,0.000037917125,0.000044972083,0.000021071539],"domain_scores_gemma":[0.99922097,0.00027885314,0.0002728683,0.000076397824,0.00005671873,0.000094177456],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00025364658,0.000117978125,0.00016305016,0.00091606716,0.00016325925,0.00024453664,0.00013913501,0.00018933142,0.0009934197],"category_scores_gemma":[0.0017598162,0.00011015257,0.00008767757,0.00085343764,0.00032368142,0.00013759873,0.0001992819,0.00026555493,0.00008497068],"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":[0.0012588057,0.000050214414,0.9176854,0.00007004188,0.00013139243,0.0012400879,0.00031308644,0.00059580867,0.06442568,0.00046216312,0.000245172,0.013522201],"study_design_scores_gemma":[0.0000036757258,0.00003278671,0.9965468,0.000002979491,0.000021670918,0.0006737521,0.00004725488,0.00025835514,0.0019143734,0.00027373727,0.0002209622,0.0000036064225],"about_ca_topic_score_codex":0.001460559,"about_ca_topic_score_gemma":0.001374485,"teacher_disagreement_score":0.001460559,"about_ca_system_score_codex":0.00024215225,"about_ca_system_score_gemma":0.00015005888,"threshold_uncertainty_score":0.0033233762},"labels":[],"label_agreement":null},{"id":"W2772621846","doi":"10.1002/pd.5198","title":"Nonisolated diaphragmatic hernia in Simpson‐Golabi‐Behmel syndrome","year":2017,"lang":"en","type":"article","venue":"Prenatal Diagnosis","topic":"Genetic Syndromes and Imprinting","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":"Hospital for Sick Children; University of Toronto; Mount Sinai Hospital","funders":"","keywords":"Congenital diaphragmatic hernia; Medicine; Prenatal diagnosis; Autopsy; Fetus; Diaphragmatic hernia; Omphalocele; Genetic testing; Pathology; Hernia; Surgery; Pregnancy; Internal medicine; Biology; Genetics","score_opus":0.010382595637977698,"score_gpt":0.2536748326890288,"score_spread":0.2432922370510511,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2772621846","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9977633,0.001354848,0.00022173338,0.00005490343,0.000010949753,0.000004716208,0.000035271245,0.0000064214055,0.00054784125],"genre_scores_gemma":[0.9995301,0.00020707067,0.00014926949,0.000019755966,0.000018554818,0.0000012968138,0.000024832927,0.0000012744558,0.00004789553],"study_design_codex":"observational","study_design_gemma":"case_report","domain_scores_codex":[0.9997266,0.00006983569,0.00004493949,0.000042438074,0.00006717519,0.000049002643],"domain_scores_gemma":[0.99872786,0.0005189119,0.00046902974,0.000053184463,0.00005192807,0.0001790638],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00029044095,0.00026967938,0.00021392018,0.0006431515,0.00026777523,0.00025926056,0.0002678567,0.00046010167,0.0015438154],"category_scores_gemma":[0.0025503628,0.00016125492,0.0001529011,0.0004047924,0.00063988566,0.0002451221,0.00041776913,0.00030017848,0.00017490202],"study_design_candidate":"case_report","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00019181971,0.000032344426,0.71849173,0.00017893617,0.000044547025,0.2647333,0.00034765078,0.00013794255,0.0054917973,0.000282359,0.0003373243,0.009730262],"study_design_scores_gemma":[0.000031585387,0.00014318053,0.26402652,0.00004045801,0.00003239454,0.7327566,0.00029750372,0.00020092938,0.0017092634,0.00017811987,0.00057592243,0.0000075293096],"about_ca_topic_score_codex":0.0007611513,"about_ca_topic_score_gemma":0.0009319009,"teacher_disagreement_score":0.0015438154,"about_ca_system_score_codex":0.0001923441,"about_ca_system_score_gemma":0.0002830774,"threshold_uncertainty_score":0.0051645637},"labels":[],"label_agreement":null},{"id":"W2784138807","doi":"10.1098/rsbl.2017.0694","title":"A genetic locus for paranoia","year":2018,"lang":"en","type":"article","venue":"Biology Letters","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","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":"University of Alberta; Simon Fraser University","funders":"Natural Sciences and Engineering Research Council of Canada","keywords":"Paranoia; Biology; Autism; Locus (genetics); Genetics; Single-nucleotide polymorphism; Psychosis; Phenotype; Autism spectrum disorder; Genomic imprinting; Gene; Population; Genotype; Psychology; Developmental psychology; Gene expression; Psychiatry; Medicine","score_opus":0.010290541977726157,"score_gpt":0.2522138954187322,"score_spread":0.24192335344100602,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2784138807","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9968413,0.00022500697,0.0010402823,0.000328689,0.000013817446,0.000012340886,0.00014912713,0.000041731324,0.0013478104],"genre_scores_gemma":[0.9981811,0.00015724346,0.001122815,0.00005450751,0.000013440019,0.0000074095747,0.000096212614,0.000008411504,0.0003588253],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.99967146,0.00009806295,0.000022223763,0.00008870306,0.000086442175,0.000033260287],"domain_scores_gemma":[0.9993174,0.00027221517,0.00020279615,0.000051911473,0.000033933844,0.00012174588],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00030986665,0.0005059044,0.00022662205,0.00078843866,0.00046308513,0.00033912086,0.0003104678,0.0005879063,0.0031556515],"category_scores_gemma":[0.0012770535,0.00016917121,0.0003562475,0.00053461513,0.0006597863,0.00016779652,0.000764868,0.00053852174,0.00016374551],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0023896613,0.00033733918,0.42597055,0.00029278142,0.0005803685,0.055949662,0.0034810374,0.0008974572,0.44896325,0.014069724,0.0018004682,0.045267694],"study_design_scores_gemma":[0.0001530323,0.0006147729,0.88553786,0.00015680066,0.0004101925,0.08170204,0.0008624102,0.003514051,0.015825398,0.0067042443,0.004425348,0.000093744755],"about_ca_topic_score_codex":0.0013544809,"about_ca_topic_score_gemma":0.0011390413,"teacher_disagreement_score":0.0031556515,"about_ca_system_score_codex":0.00023071232,"about_ca_system_score_gemma":0.00035646107,"threshold_uncertainty_score":0.010556698},"labels":[],"label_agreement":null},{"id":"W2785962058","doi":"10.1159/000484532","title":"A Clinical Review of Generalized Overgrowth Syndromes in the Era of Massively Parallel Sequencing","year":2018,"lang":"en","type":"review","venue":"Molecular Syndromology","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":47,"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 Children's Hospital; University of British Columbia","funders":"","keywords":"Medicine; Massive parallel sequencing; Mendelian inheritance; Phenotype; DNA sequencing; Bioinformatics; Biology; Genetics; Gene","score_opus":0.052388509760893036,"score_gpt":0.35853683278497234,"score_spread":0.3061483230240793,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2785962058","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":[0.0001923284,0.9970981,0.00031604044,0.0006023279,0.00038169266,0.000007175525,0.000044648383,0.000016949345,0.0013407717],"genre_scores_gemma":[0.00098808,0.9965814,0.0007306833,0.00056908384,0.00035186962,0.000009260972,0.000090316884,0.000005362293,0.00067397277],"study_design_codex":"design_other","study_design_gemma":"systematic_review","domain_scores_codex":[0.9997131,0.000053139334,0.00007785148,0.000046281722,0.000091109745,0.000018425511],"domain_scores_gemma":[0.9992931,0.0003681145,0.0001008076,0.000018892766,0.00016446951,0.000054604567],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0005818956,0.00073338905,0.0009867004,0.0038722332,0.00031392608,0.00085549016,0.0006969078,0.0009356037,0.0036013525],"category_scores_gemma":[0.0016376426,0.00027524892,0.00047756423,0.0032012807,0.00051560835,0.0014026506,0.00064259116,0.0014899962,0.002068854],"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":[0.000048243543,0.00003421306,0.0004953834,0.020310642,0.00009842161,0.0021181267,0.0001511722,0.00037024793,0.0020948567,0.004149842,0.06751323,0.9026157],"study_design_scores_gemma":[0.000006803281,0.000037580194,0.0010894871,0.004831508,0.00008533873,0.01219984,0.00007018434,0.000055840686,0.000324102,0.001507652,0.9797722,0.000019349643],"about_ca_topic_score_codex":0.0009954623,"about_ca_topic_score_gemma":0.0017196899,"teacher_disagreement_score":0.0038722332,"about_ca_system_score_codex":0.0005095116,"about_ca_system_score_gemma":0.0012613552,"threshold_uncertainty_score":0.012047708},"labels":[],"label_agreement":null},{"id":"W2789571584","doi":"10.4274/jcrpe.0029","title":"Neonatal Features of the Prader-Willi Syndrome; The Case for Making the Diagnosis During the First Week of Life","year":2018,"lang":"en","type":"article","venue":"Journal of Clinical Research in Pediatric Endocrinology","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":28,"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":"Hospital for Sick Children","keywords":"Medicine; Hypotonia; Pediatrics; Polyhydramnios; Confounding; Retrospective cohort study; Obstetrics; Pregnancy; Fetus; Internal medicine","score_opus":0.10396025017628574,"score_gpt":0.4276925213637875,"score_spread":0.32373227118750175,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2789571584","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9448193,0.015953612,0.005594999,0.020987043,0.0013051125,0.00014786146,0.00020118979,0.00016274364,0.010828217],"genre_scores_gemma":[0.9843551,0.0061970158,0.005460589,0.0012040113,0.0019145297,0.000045404406,0.000090551315,0.00001923156,0.00071372563],"study_design_codex":"case_report","study_design_gemma":"case_report","domain_scores_codex":[0.9991536,0.00025888352,0.00010283954,0.00011978503,0.00018136711,0.00018353564],"domain_scores_gemma":[0.9975248,0.00094890676,0.00069696346,0.00011700633,0.00022606016,0.00048629747],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0011781697,0.00089883467,0.00059598644,0.0019039967,0.0010146967,0.0012295552,0.0013193632,0.0028042838,0.0011665857],"category_scores_gemma":[0.0112651605,0.00054921553,0.00041630334,0.00050967897,0.0013409996,0.002351899,0.0008372795,0.003470366,0.00053326954],"study_design_candidate":"case_report","study_design_consensus":"case_report","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00017985751,0.00007499486,0.46913007,0.00017171586,0.000021046804,0.50010985,0.0011437046,0.00041475406,0.0031711943,0.0009957416,0.0042124353,0.020374566],"study_design_scores_gemma":[0.000023432736,0.00020170143,0.14389537,0.000783727,0.00004079164,0.8444822,0.0030241502,0.0015713881,0.0016279875,0.0012804868,0.0029944628,0.0000743405],"about_ca_topic_score_codex":0.0034972364,"about_ca_topic_score_gemma":0.0038040713,"teacher_disagreement_score":0.0034972364,"about_ca_system_score_codex":0.0006400418,"about_ca_system_score_gemma":0.0015054331,"threshold_uncertainty_score":0.006953776},"labels":[],"label_agreement":null},{"id":"W2790406623","doi":"10.1242/jeb.164517","title":"Genomic imprinting, growth and maternal–fetal interactions","year":2018,"lang":"en","type":"review","venue":"Journal of Experimental Biology","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":99,"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; Medical Research Council Canada; Society for Endocrinology","keywords":"Genomic imprinting; Biology; Imprinting (psychology); Insulin-like growth factor 2 receptor; Genetics; Gene; Placenta; Fetus; Growth factor; Pregnancy; Insulin-like growth factor 1 receptor; Receptor; DNA methylation; Gene expression","score_opus":0.022620177964341927,"score_gpt":0.33288154678861287,"score_spread":0.31026136882427097,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2790406623","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":[0.6726987,0.24628155,0.023343144,0.0036308544,0.00045490006,0.00003045159,0.0015276883,0.0003684409,0.051664334],"genre_scores_gemma":[0.9620951,0.029925615,0.0018604455,0.00025760307,0.0001651218,0.000017428707,0.00035346052,0.000028413853,0.0052968715],"study_design_codex":"bench_or_experimental","study_design_gemma":"not_applicable","domain_scores_codex":[0.9998412,0.000035381898,0.000006618873,0.00004880114,0.000044704695,0.000023257742],"domain_scores_gemma":[0.9996971,0.000086096705,0.00012709096,0.00001678954,0.000022921611,0.000050094102],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00023656758,0.000253223,0.00017072343,0.0003792441,0.0001463513,0.00046010432,0.00027139075,0.00022997218,0.001665894],"category_scores_gemma":[0.00046631304,0.00009039117,0.00011134879,0.00031472408,0.0006029788,0.0002934677,0.00043420147,0.00043245786,0.00027894648],"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":[0.00088812114,0.00014350966,0.05875963,0.001035034,0.00036600378,0.0028153367,0.0005751823,0.0035609629,0.5158752,0.04473821,0.0055481275,0.36569473],"study_design_scores_gemma":[0.000064406886,0.0006215314,0.6780114,0.00036201885,0.0003401203,0.004771347,0.0005870981,0.0055868416,0.13846599,0.058230855,0.11283971,0.00011865427],"about_ca_topic_score_codex":0.0012979592,"about_ca_topic_score_gemma":0.0011477743,"teacher_disagreement_score":0.001665894,"about_ca_system_score_codex":0.00048325953,"about_ca_system_score_gemma":0.00018164174,"threshold_uncertainty_score":0.0055729747},"labels":[],"label_agreement":null},{"id":"W2790585426","doi":"10.1007/978-1-4939-7710-9_14","title":"A Protocol for Epigenetic Imprinting Analysis with RNA-Seq Data","year":2018,"lang":"en","type":"article","venue":"Methods in molecular biology","topic":"Genetic Syndromes and Imprinting","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; Saskatchewan Research Council (Canada); National Research Council Canada","funders":"","keywords":"Genomic imprinting; Epigenetics; Biology; Imprinting (psychology); Arabidopsis; Genetics; Gene; Computational biology; Transcriptome; DNA methylation; Gene expression","score_opus":0.059478134429637106,"score_gpt":0.4539570101624232,"score_spread":0.39447887573278606,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2790585426","genre_codex":"methods","genre_gemma":"protocol","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"protocol","genre_consensus":null,"domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.006199364,0.00079627,0.76423883,0.0005020982,0.001387831,0.011807577,0.15607707,0.045637947,0.013352988],"genre_scores_gemma":[0.0100269,0.00059583306,0.8093256,0.0011650536,0.00016944535,0.042813376,0.10736932,0.008649043,0.019885462],"study_design_codex":"bench_or_experimental","study_design_gemma":"not_applicable","domain_scores_codex":[0.9957325,0.0007906706,0.00067759794,0.0012670355,0.0010375817,0.0004947451],"domain_scores_gemma":[0.99630475,0.001082755,0.00013865839,0.0016093078,0.0006518993,0.00021261693],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0035947997,0.0037782842,0.0021997248,0.004177683,0.0041478663,0.0025667483,0.0037560598,0.0026927064,0.07464214],"category_scores_gemma":[0.0062265364,0.0048086843,0.0031463664,0.0027460547,0.0014549508,0.0010451912,0.0022675379,0.008438949,0.06740654],"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":[0.0010355271,0.00053359574,0.002397721,0.003539262,0.0006497633,0.0013348274,0.0006616971,0.0055635395,0.70089835,0.013245705,0.18606761,0.084072344],"study_design_scores_gemma":[0.000633738,0.00035393427,0.0050543905,0.0004268768,0.00031818275,0.0013896346,0.00015969857,0.015716173,0.3708961,0.015400709,0.5891822,0.00046841704],"about_ca_topic_score_codex":0.0032204923,"about_ca_topic_score_gemma":0.013763444,"teacher_disagreement_score":0.07464214,"about_ca_system_score_codex":0.001186753,"about_ca_system_score_gemma":0.0038660348,"threshold_uncertainty_score":0.24970281},"labels":[],"label_agreement":null},{"id":"W2790668598","doi":"10.1016/j.jpeds.2017.12.083","title":"Pseudopseudohypoparathyroidism: A Diagnostic Consideration in a Patient with Brachydactyly","year":2018,"lang":"en","type":"article","venue":"The Journal of Pediatrics","topic":"Genetic Syndromes and Imprinting","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; Montreal Children's Hospital","funders":"","keywords":"Medicine; GNAS complex locus; Brachydactyly; Pseudohypoparathyroidism; Parathyroid hormone; Physical examination; Short stature; Pediatrics; Anatomy; Surgery; Internal medicine","score_opus":0.006819442429877253,"score_gpt":0.22325190541952158,"score_spread":0.21643246298964433,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2790668598","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.97523266,0.0027025423,0.0028280297,0.009274189,0.00044558258,0.0001486306,0.0003760792,0.00019994524,0.0087922355],"genre_scores_gemma":[0.99529654,0.00073195604,0.001941802,0.0006998455,0.00067932176,0.000030858966,0.00009744941,0.000039036215,0.00048331238],"study_design_codex":"case_report","study_design_gemma":"case_report","domain_scores_codex":[0.9991781,0.00007983428,0.00013714975,0.00018524412,0.00017873054,0.00024088306],"domain_scores_gemma":[0.99684095,0.0014112176,0.00036985858,0.00013978005,0.0001649654,0.0010733526],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0004011482,0.002263316,0.001138212,0.003874596,0.002839551,0.0017963637,0.0019065249,0.0062457384,0.0026656622],"category_scores_gemma":[0.007404657,0.0011574108,0.0011561827,0.0016438774,0.0025921306,0.0020747022,0.0020891312,0.003929731,0.0007605655],"study_design_candidate":"case_report","study_design_consensus":"case_report","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.000027521779,0.000009890914,0.0047686254,0.000009861028,0.000002075541,0.99379313,0.00006167959,0.000047743724,0.00070799974,0.0000879194,0.000110390945,0.0003731596],"study_design_scores_gemma":[0.000008530167,0.000046674577,0.004317786,0.000008411922,0.000009799425,0.99409914,0.00013315548,0.00029525333,0.0006925407,0.00017210397,0.00020712458,0.000009558729],"about_ca_topic_score_codex":0.002047177,"about_ca_topic_score_gemma":0.0017972498,"teacher_disagreement_score":0.0062457384,"about_ca_system_score_codex":0.0013628788,"about_ca_system_score_gemma":0.0013497871,"threshold_uncertainty_score":0.009888411},"labels":[],"label_agreement":null},{"id":"W2790744144","doi":"10.3945/an.117.016253","title":"Energy Metabolism Profile in Individuals with Prader-Willi Syndrome and Implications for Clinical Management: A Systematic Review","year":2017,"lang":"en","type":"review","venue":"Advances in Nutrition","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":55,"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":"Body mass index; Thermogenesis; Resting energy expenditure; Endocrinology; Lean body mass; Energy expenditure; Medicine; Weight management; Internal medicine; Weight loss; Obesity; Weight gain; Body weight","score_opus":0.04971778163201943,"score_gpt":0.39853241773752535,"score_spread":0.3488146361055059,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2790744144","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":[0.00030046588,0.9993506,0.000035149988,0.00008333259,0.000031095995,0.0000048107167,0.00011824233,0.0000014757657,0.00007486774],"genre_scores_gemma":[0.0022119305,0.9972525,0.00015746632,0.0001658511,0.00004660941,0.0000102145605,0.000112570124,8.872554e-7,0.00004184556],"study_design_codex":"design_other","study_design_gemma":"systematic_review","domain_scores_codex":[0.9995372,0.00008501021,0.00017607772,0.000091292,0.00008894053,0.000021544593],"domain_scores_gemma":[0.99842215,0.0010811454,0.00030814655,0.000021175762,0.0001376379,0.00002985487],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0010335225,0.00082388916,0.0032265163,0.0030317323,0.00018712107,0.0011368439,0.0008285195,0.0009266417,0.0027114272],"category_scores_gemma":[0.0038759946,0.0003294789,0.0020817341,0.0039494135,0.00029042957,0.0009617699,0.0007302058,0.0008132085,0.00025522045],"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":[0.0007136768,0.00008254973,0.0082860775,0.39498362,0.012024288,0.0005141286,0.00021636098,0.00045857814,0.0006010901,0.000935805,0.01645071,0.56473315],"study_design_scores_gemma":[0.00072432065,0.00042714344,0.050203554,0.4783979,0.0982355,0.0053510843,0.00088335254,0.00044971905,0.000645299,0.003288758,0.3611231,0.00027013873],"about_ca_topic_score_codex":0.0037002214,"about_ca_topic_score_gemma":0.011294244,"teacher_disagreement_score":0.0037002214,"about_ca_system_score_codex":0.000541369,"about_ca_system_score_gemma":0.0018509659,"threshold_uncertainty_score":0.009070575},"labels":[],"label_agreement":null},{"id":"W2792735683","doi":"10.1097/bpo.0000000000001123","title":"Growth Friendly Surgery and Serial Cast Correction in the Treatment of Early-onset Scoliosis for Patients With Prader-Willi Syndrome","year":2018,"lang":"en","type":"article","venue":"Journal of Pediatric Orthopaedics","topic":"Genetic Syndromes and Imprinting","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":"Izaak Walton Killam Health Centre; Dalhousie University","funders":"","keywords":"Medicine; Scoliosis; Kyphosis; Body mass index; Surgery; Nuclear medicine; Internal medicine; Radiography","score_opus":0.008634636247402688,"score_gpt":0.22499391837269508,"score_spread":0.2163592821252924,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2792735683","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9988049,0.00074843265,0.00006092327,0.000042423013,0.0000042318616,0.000010191977,0.000053127274,0.0000027083372,0.00027301963],"genre_scores_gemma":[0.9990884,0.00037179052,0.00025271086,0.000023020373,0.0000128859,0.000009953294,0.00015384365,9.950802e-7,0.000086323154],"study_design_codex":"observational","study_design_gemma":"case_report","domain_scores_codex":[0.9998369,0.000042484913,0.000024143701,0.00002155015,0.00004482297,0.000029996389],"domain_scores_gemma":[0.9995945,0.00007963618,0.00018558341,0.000011963297,0.000024663199,0.00010366813],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.000250951,0.00016149282,0.00024320108,0.00032098027,0.0002644929,0.00019637747,0.00018800168,0.00018388414,0.0007094466],"category_scores_gemma":[0.0007167827,0.00005773258,0.0002609847,0.0003332969,0.00014584186,0.00011543884,0.00020856687,0.00022081827,0.000079358935],"study_design_candidate":"case_report","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00073841645,0.00030319957,0.9586933,0.00008441803,0.00006538567,0.0031443976,0.00011149654,0.00020667032,0.0025521605,0.000025359752,0.00024653197,0.033828516],"study_design_scores_gemma":[0.00009416243,0.0015592623,0.98542506,0.000029469094,0.000057279696,0.010932519,0.0001589915,0.0002030424,0.00096550654,0.000024964153,0.0005437631,0.000006050787],"about_ca_topic_score_codex":0.00087583734,"about_ca_topic_score_gemma":0.002899691,"teacher_disagreement_score":0.00087583734,"about_ca_system_score_codex":0.0001543756,"about_ca_system_score_gemma":0.00054018793,"threshold_uncertainty_score":0.0023733377},"labels":[],"label_agreement":null},{"id":"W2793616120","doi":"10.1016/j.ymgme.2018.02.018","title":"Chronic diazoxide treatment decreases fat mass and improves endurance capacity in an obese mouse model of Prader-Willi syndrome","year":2018,"lang":"en","type":"article","venue":"Molecular Genetics and Metabolism","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":21,"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","funders":"University of Alberta; Foundation for Prader-Willi Research","keywords":"Diazoxide; Endocrinology; Internal medicine; Medicine; Fat mass; Obesity; Metabolic syndrome; Insulin","score_opus":0.018840384411991713,"score_gpt":0.2380819341873577,"score_spread":0.219241549775366,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2793616120","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99768114,0.00047733224,0.00090707303,0.00016616262,0.000036831738,0.000012604623,0.00031502303,0.00009341755,0.0003102882],"genre_scores_gemma":[0.99107516,0.0017815514,0.0026272775,0.000095004194,0.00002841796,0.00007986191,0.0005621924,0.00006582392,0.0036846544],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99981195,0.000031620493,0.000022738363,0.000042104464,0.000055648485,0.000035892786],"domain_scores_gemma":[0.99973005,0.00002865088,0.000099927514,0.000024255467,0.0000148974,0.000102299186],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00019151035,0.0007791544,0.0005083256,0.0007724572,0.00020933489,0.00030013325,0.0005167171,0.00056713837,0.0017163181],"category_scores_gemma":[0.00015692263,0.00032070375,0.00039513328,0.00022461909,0.0005737678,0.00034654405,0.0003258478,0.0013998842,0.00030501955],"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":[0.0008993275,0.00016101173,0.00033117272,0.000029561837,0.000018716584,0.00017679446,0.000016526434,0.00007828816,0.9968867,0.00008843892,0.000054357246,0.0012591825],"study_design_scores_gemma":[0.00044270675,0.0028519498,0.014429772,0.000026038308,0.00020818284,0.000958021,0.00015500875,0.0016830991,0.97668684,0.00026712855,0.0022575557,0.000033764492],"about_ca_topic_score_codex":0.0009285574,"about_ca_topic_score_gemma":0.0017423128,"teacher_disagreement_score":0.0017163181,"about_ca_system_score_codex":0.00029929544,"about_ca_system_score_gemma":0.0002957529,"threshold_uncertainty_score":0.005741656},"labels":[],"label_agreement":null},{"id":"W2797591163","doi":"10.1681/asn.2018030288","title":"Using Large Datasets to Understand CKD","year":2018,"lang":"en","type":"letter","venue":"Journal of the American Society of Nephrology","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":0,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Children’s Health Research Institute; Western University","funders":"Canadian Institutes of Health Research","keywords":"Medicine; Computer science; Intensive care medicine","score_opus":0.03024405026960725,"score_gpt":0.299838997234843,"score_spread":0.2695949469652357,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2797591163","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":[0.06232794,0.01808071,0.10353438,0.039503995,0.0018443458,0.0011692758,0.7540071,0.0041083056,0.015423995],"genre_scores_gemma":[0.21307085,0.007680379,0.11065086,0.011292649,0.0015721937,0.0030614657,0.6496087,0.00085634616,0.0022066615],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9872399,0.006699575,0.0013432087,0.002899041,0.0013533358,0.00046503596],"domain_scores_gemma":[0.97080594,0.017780216,0.0025581436,0.005855275,0.00215759,0.0008428733],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.015299133,0.0014095523,0.0020033647,0.007107255,0.0013350339,0.00490936,0.002252713,0.0025794352,0.008875599],"category_scores_gemma":[0.05976267,0.00081585563,0.0028115497,0.009955092,0.000825785,0.004176542,0.0048147696,0.0034038788,0.002857568],"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":[0.0009883408,0.00044381933,0.38398546,0.004389841,0.008064524,0.0010026358,0.0007171989,0.024958964,0.0012837416,0.030638753,0.3341059,0.20942076],"study_design_scores_gemma":[0.00071097334,0.00026578474,0.21370651,0.0026722392,0.0022821282,0.0009919188,0.0011887372,0.062946506,0.0010878291,0.2316883,0.48208278,0.00037631474],"about_ca_topic_score_codex":0.011105642,"about_ca_topic_score_gemma":0.013042171,"teacher_disagreement_score":0.015299133,"about_ca_system_score_codex":0.0019779643,"about_ca_system_score_gemma":0.003066851,"threshold_uncertainty_score":0.080910504},"labels":[],"label_agreement":null},{"id":"W2797685235","doi":"10.1016/j.jpsychires.2018.04.012","title":"The impact of body mass index in gene expression of reelin pathway mediators in individuals with schizophrenia and mood disorders: A post-mortem study","year":2018,"lang":"en","type":"article","venue":"Journal of Psychiatric Research","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","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":"University Health Network; McMaster University; University of Toronto","funders":"National Institute of Mental Health","keywords":"Reelin; Schizophrenia (object-oriented programming); Body mass index; Hippocampus; Internal medicine; Medicine; Mood disorders; Psychology; Oncology; Endocrinology; Bioinformatics; Psychiatry; Biology; Receptor","score_opus":0.012338122558814299,"score_gpt":0.33025873478642914,"score_spread":0.31792061222761486,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2797685235","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9995732,0.000108622924,0.00003959687,0.000011360879,0.0000026363257,0.0000027758579,0.00007309372,0.0000011663556,0.00018756997],"genre_scores_gemma":[0.9993363,0.000052692107,0.000038958617,0.000015698472,0.0000040445716,0.0000043097043,0.00007490851,0.000002504355,0.00047055734],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9998965,0.00002611183,0.000007740255,0.0000337184,0.000015345406,0.000020515923],"domain_scores_gemma":[0.99976975,0.00006208071,0.00007875673,0.000029259734,0.000020500824,0.000039593026],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00018898728,0.00028195584,0.00033755953,0.00049414684,0.00043847464,0.00043469245,0.00019301745,0.00035085191,0.0016587094],"category_scores_gemma":[0.00051768386,0.00027521903,0.00032817447,0.00034769566,0.00034936363,0.00022783075,0.00029481627,0.00039226608,0.00023111147],"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":[0.0079889055,0.00035851987,0.93843675,0.00003709764,0.00040207923,0.0017654862,0.00080387475,0.00010687418,0.043572064,0.0001023827,0.00012586107,0.006300158],"study_design_scores_gemma":[0.000009868298,0.00019187853,0.99905735,0.0000013953389,0.00004513043,0.00021369902,0.00009528625,0.00003475573,0.00028493622,0.000017653285,0.000045869776,0.0000022891402],"about_ca_topic_score_codex":0.0023025484,"about_ca_topic_score_gemma":0.003278145,"teacher_disagreement_score":0.0023025484,"about_ca_system_score_codex":0.00021112569,"about_ca_system_score_gemma":0.000120130746,"threshold_uncertainty_score":0.005548954},"labels":[],"label_agreement":null},{"id":"W2799463622","doi":"10.1111/gbb.12483","title":"Distinct chromatin structures at the monoamine oxidase‐A promoter correlate with allele‐specific expression in SH‐SY5Y cells","year":2018,"lang":"en","type":"article","venue":"Genes Brain & Behavior","topic":"Genetic Syndromes and Imprinting","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":"National Institute for Health and Care Research; Medical Research Council Canada; University of Liverpool; Wellcome Trust","keywords":"Epigenetics; Allele; Biology; Monoamine oxidase A; Genetics; Promoter; DNA methylation; Transcription factor; Gene; Gene expression","score_opus":0.009971459689510477,"score_gpt":0.23516728401833578,"score_spread":0.22519582432882532,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2799463622","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99493474,0.001138828,0.0014852402,0.000065698216,0.000023961142,0.000009691413,0.0006432384,0.000040565035,0.001658089],"genre_scores_gemma":[0.99334043,0.0005337174,0.0011186968,0.00004904586,0.000010857184,0.000023726892,0.0012163552,0.000016728887,0.0036904286],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99988735,0.000008253176,0.000008262831,0.000037201706,0.000034654575,0.000024292112],"domain_scores_gemma":[0.999882,0.000025182793,0.00003369782,0.000018357723,0.000013607945,0.000027197117],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00008321306,0.000119169395,0.00015334773,0.00024232293,0.00017580809,0.00024137957,0.00009065567,0.00016403946,0.001875474],"category_scores_gemma":[0.00008771378,0.0001534355,0.00018929911,0.00015277635,0.0002276451,0.00013574194,0.00021605837,0.00036834867,0.00057231856],"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":[0.00004580763,0.000008500406,0.00066491915,0.00000756212,0.0000036662866,0.000038184604,0.000031645977,0.000008991767,0.9986186,0.000056314537,0.000024790108,0.00049087335],"study_design_scores_gemma":[0.000017395683,0.00024689367,0.1553718,0.00000716607,0.00002071332,0.00061004586,0.00013383839,0.00066847476,0.84046316,0.00010127811,0.0023517457,0.0000075010653],"about_ca_topic_score_codex":0.0013546293,"about_ca_topic_score_gemma":0.0026653556,"teacher_disagreement_score":0.001875474,"about_ca_system_score_codex":0.00022404436,"about_ca_system_score_gemma":0.00013028701,"threshold_uncertainty_score":0.0062740445},"labels":[],"label_agreement":null},{"id":"W2799899236","doi":"10.5206/uwomj.v86is1.2108","title":"Decreased level of consciousness in a toddler with overgrowth syndrome","year":2018,"lang":"en","type":"article","venue":"University of Western Ontario Medical Journal","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":0,"is_retracted":false,"has_abstract":true,"route_ca_aff":false,"route_ca_fund":false,"route_ca_venue":true,"route_about_ca":false,"ca_institutions":"","funders":"","keywords":"Toddler; Medicine; Pediatrics; Disease; Exome; Exome sequencing; Intensive care medicine; Mutation; Bioinformatics; Psychology; Genetics; Internal medicine; Developmental psychology; Gene; Biology","score_opus":0.018023905711904882,"score_gpt":0.21929992530296719,"score_spread":0.2012760195910623,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2799899236","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9918075,0.0012722841,0.0009960582,0.0016730838,0.0001142793,0.00003910309,0.00013367778,0.00009962495,0.0038642625],"genre_scores_gemma":[0.998343,0.00043457758,0.00042037532,0.00035069385,0.000039912487,0.000004674016,0.00003668812,0.000011092771,0.00035903172],"study_design_codex":"case_report","study_design_gemma":"case_report","domain_scores_codex":[0.9997148,0.00002878634,0.000038962633,0.000053444463,0.00006894627,0.00009499036],"domain_scores_gemma":[0.99947137,0.00012617833,0.0001586663,0.000021925483,0.00004904576,0.00017271026],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00017164157,0.0010200342,0.000697561,0.0011631132,0.0011090746,0.0006018007,0.00049430184,0.0011371857,0.0009630307],"category_scores_gemma":[0.0019767447,0.00030367612,0.00038607814,0.0007931862,0.0011573237,0.00040307982,0.0009539974,0.0014960371,0.0002142815],"study_design_candidate":"case_report","study_design_consensus":"case_report","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.000038231185,0.000014014632,0.026515536,0.00001766753,0.000010348357,0.9696297,0.00028529885,0.00006201185,0.0014659124,0.000115748815,0.00027859214,0.0015668643],"study_design_scores_gemma":[0.000007727931,0.000078467434,0.047652643,0.00002889757,0.000019056897,0.95029503,0.00042199594,0.000202804,0.00067388144,0.00022862553,0.00037731865,0.000013462259],"about_ca_topic_score_codex":0.013111827,"about_ca_topic_score_gemma":0.017929977,"teacher_disagreement_score":0.013111827,"about_ca_system_score_codex":0.0012212232,"about_ca_system_score_gemma":0.0008728057,"threshold_uncertainty_score":0.026071012},"labels":[],"label_agreement":null},{"id":"W2800622687","doi":"10.1530/rep-18-0051","title":"Imprint stability and plasticity during development","year":2018,"lang":"en","type":"review","venue":"Reproduction","topic":"Genetic Syndromes and Imprinting","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":"Terry Fox Research Institute","funders":"Biotechnology and Biological Sciences Research Council; Economic and Social Research Council; Medical Research Council","keywords":"Genomic imprinting; Imprinting (psychology); Biology; DNA methylation; Genome; Locus (genetics); Evolutionary biology; Genetics; Computational biology; Gene; Gene expression","score_opus":0.03589163940571044,"score_gpt":0.2837698675764381,"score_spread":0.24787822817072763,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2800622687","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":[0.00053002493,0.99586856,0.00040119278,0.00033694677,0.00015863593,0.0000037205552,0.00003511069,0.00001659084,0.0026492656],"genre_scores_gemma":[0.0054230746,0.9927331,0.00018690302,0.00015614336,0.00016924166,0.0000064019196,0.00004314088,0.0000040730624,0.0012778401],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.9998311,0.000024335313,0.000018138184,0.00004351282,0.000059889273,0.000023124188],"domain_scores_gemma":[0.99980396,0.000097258526,0.000030201292,0.000010603976,0.00003637233,0.00002174299],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00042061374,0.00038404815,0.0006381025,0.0012035891,0.00021709169,0.00085001596,0.0006560664,0.0008093019,0.0026885134],"category_scores_gemma":[0.00060040795,0.00018529836,0.00025591295,0.0009698213,0.0009666944,0.0008623777,0.0006592627,0.0009882739,0.0013530956],"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":[0.000089595735,0.000022624008,0.00086915185,0.009277865,0.00006280031,0.000602441,0.00017515029,0.0006320203,0.010584005,0.016899988,0.012532317,0.94825214],"study_design_scores_gemma":[0.0000064393143,0.000053752865,0.0032719788,0.0013476867,0.00004981598,0.0026333786,0.000076949276,0.00009062483,0.0041851797,0.006668452,0.9815962,0.000019537822],"about_ca_topic_score_codex":0.0008141078,"about_ca_topic_score_gemma":0.0011159154,"teacher_disagreement_score":0.0026885134,"about_ca_system_score_codex":0.0007250268,"about_ca_system_score_gemma":0.00068681914,"threshold_uncertainty_score":0.008994043},"labels":[],"label_agreement":null},{"id":"W2804089987","doi":"10.1016/j.yhbeh.2018.05.011","title":"Wnt-2b in the intermediate hyperpallium apicale of the telencephalon is critical for the thyroid hormone-mediated opening of the sensitive period for filial imprinting in domestic chicks (Gallus gallus domesticus)","year":2018,"lang":"en","type":"article","venue":"Hormones and Behavior","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":9,"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 Musculoskeletal Health and Arthritis; Japan Society for the Promotion of Science; Foundation for Promotion of Cancer Research; Ministry of Education, Culture, Sports, Science and Technology; National Cancer Institute; Japan Foundation of Applied Enzymology; Uehara Memorial Foundation; Naito Foundation","keywords":"Imprinting (psychology); Cerebrum; Wnt signaling pathway; Period (music); Hatching; Internal medicine; Triiodothyronine; Endocrinology; Hormone; Biology; Chemistry; Cell biology; Central nervous system; Animal science; Gene; Biochemistry; Medicine; Signal transduction","score_opus":0.012110408448500833,"score_gpt":0.2824105187629376,"score_spread":0.2703001103144368,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2804089987","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9896129,0.0017981147,0.00565919,0.00021448023,0.000052943884,0.000014215124,0.00044408542,0.00012311265,0.0020810014],"genre_scores_gemma":[0.99201035,0.00029679143,0.0015439738,0.00007905737,0.000007015188,0.00001655196,0.0005603783,0.000077816556,0.005408088],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9998429,0.00001554976,0.000015521313,0.00003609481,0.00004826299,0.00004165159],"domain_scores_gemma":[0.99977726,0.00002384887,0.000096402866,0.00001475563,0.000020391239,0.00006733176],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00012337635,0.00031519402,0.00024049974,0.00034904055,0.0003522137,0.00064462645,0.0003895773,0.00047754674,0.0017127661],"category_scores_gemma":[0.00019307247,0.00047888074,0.00025359893,0.00009674983,0.0004718164,0.00037573115,0.00050176797,0.00081667345,0.00080795307],"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":[0.00007091489,0.000003454842,0.00019028626,0.000016654309,0.0000025073102,0.000058737383,0.000009841863,0.000034364057,0.9991272,0.00019646068,0.000025519914,0.00026411124],"study_design_scores_gemma":[0.00006537611,0.00005591227,0.04944972,0.000024586212,0.000046633522,0.0006278926,0.00013613005,0.0022999328,0.9423054,0.00028664246,0.0046876404,0.0000142379195],"about_ca_topic_score_codex":0.0028455441,"about_ca_topic_score_gemma":0.007641194,"teacher_disagreement_score":0.0028455441,"about_ca_system_score_codex":0.0006358945,"about_ca_system_score_gemma":0.0004408768,"threshold_uncertainty_score":0.0057297945},"labels":[],"label_agreement":null},{"id":"W2808484533","doi":"10.1186/s12864-018-4835-2","title":"Development and application of an integrated allele-specific pipeline for methylomic and epigenomic analysis (MEA)","year":2018,"lang":"en","type":"article","venue":"BMC Genomics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":20,"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; Simon Fraser University; University of British Columbia","funders":"Natural Sciences and Engineering Research Council of Canada; Canadian Institutes of Health Research; Killam Trusts; U.S. Department of Veterans Affairs","keywords":"Epigenomics; Biology; Indel; Allele; Genetics; Computational biology; DNA methylation; Epigenome; Gene; Gene expression; Single-nucleotide polymorphism; Genotype","score_opus":0.01811735396814028,"score_gpt":0.25624073942530323,"score_spread":0.23812338545716294,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2808484533","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":[0.012423993,0.00025070301,0.8040555,0.00025052423,0.0001059464,0.00039575557,0.014931715,0.16606216,0.0015237314],"genre_scores_gemma":[0.05701795,0.00027954055,0.8918735,0.00036047248,0.000060805047,0.0016448841,0.032384787,0.013971471,0.0024066207],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99894494,0.00012329982,0.00010017208,0.00042542937,0.0003116656,0.0000945882],"domain_scores_gemma":[0.998245,0.0005853527,0.00018663332,0.00039864576,0.00039903674,0.00018539598],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0027084192,0.0022160956,0.0010776735,0.002309494,0.0007649667,0.0018505491,0.0020405361,0.00095915276,0.0093535045],"category_scores_gemma":[0.005112514,0.0011064818,0.0018117307,0.001212022,0.0004879769,0.0015076516,0.0027560585,0.0022715037,0.00537078],"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":[0.0019209033,0.00028466742,0.019425184,0.002029426,0.0015894587,0.0010612799,0.0010620414,0.016595464,0.45503074,0.00816956,0.08271281,0.41011858],"study_design_scores_gemma":[0.00032305738,0.00040615263,0.032256998,0.00019039921,0.00042957996,0.001241876,0.0002335175,0.3027535,0.49402246,0.021483732,0.1461733,0.00048540084],"about_ca_topic_score_codex":0.002156558,"about_ca_topic_score_gemma":0.00328502,"teacher_disagreement_score":0.0093535045,"about_ca_system_score_codex":0.0006776213,"about_ca_system_score_gemma":0.001968067,"threshold_uncertainty_score":0.03129065},"labels":[],"label_agreement":null},{"id":"W2809162318","doi":"10.1016/j.rehab.2018.06.001","title":"Test-retest reliability of the Bruininks-Oseretsky Test of Motor Proficiency, Second Edition for youth with Prader-Willi syndrome","year":2018,"lang":"en","type":"letter","venue":"Annals of Physical and Rehabilitation Medicine","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","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":"St. Francis Xavier University","funders":"","keywords":"Test (biology); Psychology; Reliability (semiconductor); Developmental psychology; Audiology; Physical medicine and rehabilitation; Medicine; Physics","score_opus":0.01625771701906824,"score_gpt":0.26988096203585055,"score_spread":0.2536232450167823,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2809162318","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9138426,0.0070000608,0.004952956,0.045197926,0.0042856103,0.00013937663,0.001445968,0.00029033708,0.022845224],"genre_scores_gemma":[0.9892174,0.0009257829,0.002339727,0.0030268733,0.00058586634,0.00008288931,0.00043544534,0.00004268909,0.0033433158],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99799085,0.00047494695,0.0004716897,0.00035618525,0.0005429273,0.00016332125],"domain_scores_gemma":[0.9914739,0.0043426664,0.00045075154,0.000482512,0.0030091798,0.00024094844],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00243629,0.00045256407,0.00068753294,0.0007347112,0.0005374907,0.0006469462,0.0007489417,0.0018790532,0.0014531561],"category_scores_gemma":[0.02218066,0.00023142213,0.00056095317,0.00037131904,0.0005346539,0.0006988735,0.00045718797,0.0017933403,0.00082101027],"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":[0.00081291347,0.00031194687,0.81878597,0.0001734843,0.00030217905,0.016518276,0.0023783937,0.0006114436,0.0095667215,0.001061108,0.040652923,0.10882469],"study_design_scores_gemma":[0.000088046734,0.00052929705,0.92550695,0.00018460026,0.00024233099,0.03991494,0.0012384572,0.003565405,0.0049836677,0.0019897337,0.021657644,0.0000990206],"about_ca_topic_score_codex":0.0042353426,"about_ca_topic_score_gemma":0.005390352,"teacher_disagreement_score":0.0042353426,"about_ca_system_score_codex":0.0008529348,"about_ca_system_score_gemma":0.0005285897,"threshold_uncertainty_score":0.012884498},"labels":[],"label_agreement":null},{"id":"W2810557264","doi":"10.3390/languages3030023","title":"The Narrative Abilities of an English-Spanish Bilingual with Prader-Willi Syndrome","year":2018,"lang":"en","type":"article","venue":"Languages","topic":"Genetic Syndromes and Imprinting","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":"Wilfrid Laurier University; University of Ottawa","funders":"Universidad El Bosque","keywords":"Narrative; Linguistics; Psychology; History; Philosophy","score_opus":0.005002492442178484,"score_gpt":0.24713342296892962,"score_spread":0.24213093052675114,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2810557264","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99933714,0.00007045249,0.000033630287,0.000023273278,0.000002441999,0.000004383416,0.000016437367,0.0000015312288,0.0005108199],"genre_scores_gemma":[0.9988147,0.00014427205,0.00016876444,0.000032492324,0.0000031982063,0.0000073245033,0.00005067174,0.000002271335,0.0007762904],"study_design_codex":"observational","study_design_gemma":"case_report","domain_scores_codex":[0.9998778,0.000025458257,0.000013977313,0.000028852304,0.000028454499,0.000025432411],"domain_scores_gemma":[0.99966943,0.000080081605,0.000077430406,0.000016085864,0.0000707344,0.00008610918],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00024263804,0.00037519442,0.000336556,0.0006857932,0.00072942756,0.0005732179,0.0001855558,0.0002704784,0.0017828107],"category_scores_gemma":[0.0013554347,0.0001528017,0.00013659579,0.00017844052,0.00042086196,0.00031378513,0.0006474137,0.00027709416,0.0002904653],"study_design_candidate":"case_report","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0011089527,0.0018227149,0.70780104,0.0002741843,0.00005717086,0.10426494,0.074937575,0.00022250682,0.06398579,0.00051252055,0.000795454,0.044217177],"study_design_scores_gemma":[0.00007444012,0.0018747747,0.74856097,0.000083594045,0.000073741525,0.18013975,0.058141075,0.0007329348,0.005717808,0.00054492074,0.0039868206,0.00006908645],"about_ca_topic_score_codex":0.0062388405,"about_ca_topic_score_gemma":0.008308145,"teacher_disagreement_score":0.0062388405,"about_ca_system_score_codex":0.00030699116,"about_ca_system_score_gemma":0.0005004189,"threshold_uncertainty_score":0.012405038},"labels":[],"label_agreement":null},{"id":"W284515077","doi":"10.1016/b978-0-444-52014-2.00012-4","title":"Benign hereditary chorea","year":2011,"lang":"en","type":"review","venue":"Handbook of clinical neurology","topic":"Genetic Syndromes and Imprinting","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":"Toronto Western Hospital; University of Toronto","funders":"","keywords":"Haploinsufficiency; Chorea; Phenotype; Pathology; Neuroscience; Medicine; Psychology; Biology; Genetics; Gene","score_opus":0.11223752989189935,"score_gpt":0.39036854470936766,"score_spread":0.2781310148174683,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W284515077","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":[0.00031832673,0.9905642,0.0011725947,0.00046378325,0.0010759686,0.000014553594,0.000049025344,0.000085818276,0.0062557883],"genre_scores_gemma":[0.0033507305,0.9816081,0.0019862836,0.001058412,0.0019680907,0.000027392367,0.00021733482,0.000016652475,0.009767065],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.999833,0.000022851274,0.000023870018,0.000038975337,0.000059344435,0.000021964312],"domain_scores_gemma":[0.99983966,0.00005892879,0.000025124493,0.00000962745,0.000031943382,0.00003470945],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00026713978,0.0015048082,0.0013368572,0.004263981,0.0003377105,0.00077654934,0.0008257511,0.0010855456,0.005603648],"category_scores_gemma":[0.0005152618,0.0003258273,0.00035851507,0.0021138105,0.00077837706,0.00090839574,0.0009030509,0.0020267246,0.004070994],"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":[0.000049363814,0.000059865608,0.00022356994,0.002707087,0.00003489536,0.0018458096,0.000028627706,0.00022792598,0.0013113371,0.0019743256,0.09957359,0.8919636],"study_design_scores_gemma":[0.000037403348,0.00005346772,0.0015252643,0.0021726487,0.0000761368,0.026642969,0.00006081982,0.0001784613,0.00075647,0.0018912284,0.966574,0.00003104051],"about_ca_topic_score_codex":0.0017970796,"about_ca_topic_score_gemma":0.0047674826,"teacher_disagreement_score":0.005603648,"about_ca_system_score_codex":0.0005274113,"about_ca_system_score_gemma":0.0009637755,"threshold_uncertainty_score":0.018746018},"labels":[],"label_agreement":null},{"id":"W2855880246","doi":"10.1038/s41467-018-05208-2","title":"Nucleoporin 107, 62 and 153 mediate Kcnq1ot1 imprinted domain regulation in extraembryonic endoderm stem cells","year":2018,"lang":"en","type":"article","venue":"Nature Communications","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","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":"Children’s Health Research Institute; Western University","funders":"Canadian Institutes of Health Research; Lawson Health Research Institute; Magee-Womens Research Institute; Children's Health Research Institute; Natural Sciences and Engineering Research Council of Canada; University of Pittsburgh","keywords":"Genomic imprinting; Nucleoporin; Biology; Epigenetics; Endoderm; Cell biology; Genetics; Cellular differentiation; DNA methylation; Transcription factor; Gene; Gene expression; Nuclear protein","score_opus":0.01128368231826908,"score_gpt":0.2644159377348545,"score_spread":0.2531322554165854,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2855880246","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99718934,0.00047683425,0.0014363626,0.00003454146,0.0000038061848,0.0000041982225,0.000077061435,0.000025107336,0.00075285754],"genre_scores_gemma":[0.9971943,0.00029904113,0.0008418437,0.000018728932,0.0000018208992,0.0000070137776,0.00015615133,0.000015193992,0.0014659915],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9999063,0.000011575128,0.000008200938,0.000021731039,0.00003469005,0.000017476774],"domain_scores_gemma":[0.99989283,0.000025462426,0.000037694674,0.0000105537565,0.0000064990236,0.000026953636],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00008316436,0.00021464897,0.00014401783,0.00015369277,0.00009919481,0.00024422538,0.00020855355,0.00017633256,0.00090375845],"category_scores_gemma":[0.000099211546,0.0001625669,0.0001119533,0.00006577752,0.00023434444,0.000142465,0.00022982794,0.00022666788,0.00021824663],"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":[0.000016370279,0.0000017289084,0.00017578424,0.0000068651675,0.0000012010787,0.000019004641,0.0000047719764,0.000021929058,0.99941313,0.00006038027,0.000004227067,0.00027471472],"study_design_scores_gemma":[0.000004532177,0.00002568077,0.0060862345,0.0000012474904,0.0000060366106,0.000136919,0.0000111785885,0.0003669979,0.99286157,0.000034002776,0.00046451873,0.0000010938768],"about_ca_topic_score_codex":0.00048398814,"about_ca_topic_score_gemma":0.0011312017,"teacher_disagreement_score":0.00090375845,"about_ca_system_score_codex":0.0002568406,"about_ca_system_score_gemma":0.00013667617,"threshold_uncertainty_score":0.003023386},"labels":[],"label_agreement":null},{"id":"W2883447942","doi":"10.1136/jmedgenet-2018-105328","title":"Paternal uniparental disomy of chromosome 19 in a pair of monochorionic diamniotic twins with dysmorphic features and developmental delay","year":2018,"lang":"en","type":"article","venue":"Journal of Medical Genetics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":10,"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; Hospital for Sick Children; University of Toronto","funders":"","keywords":"Uniparental disomy; Genetics; Biology; Genomic imprinting; Exome sequencing; Imprinting (psychology); Karyotype; SNP array; Chromosome; DNA methylation; Phenotype; Single-nucleotide polymorphism; Gene; Genotype","score_opus":0.01000815464124764,"score_gpt":0.248395496992991,"score_spread":0.23838734235174336,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2883447942","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.996099,0.00044018857,0.00081679784,0.0002958456,0.00009645354,0.000053158004,0.00018088541,0.000018560151,0.0019991444],"genre_scores_gemma":[0.9979997,0.00019681682,0.0008635949,0.000095865435,0.00004787952,0.000013962599,0.00007279535,0.000008587141,0.00070068263],"study_design_codex":"case_report","study_design_gemma":"case_report","domain_scores_codex":[0.99933714,0.00008186704,0.00009366957,0.00018627352,0.00016191922,0.00013917887],"domain_scores_gemma":[0.9990281,0.00019142876,0.00024397961,0.000079902486,0.000069261645,0.00038726637],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00033041093,0.0010610936,0.00061705563,0.0016294158,0.0014815277,0.0006270871,0.0007053945,0.0010986275,0.0014711503],"category_scores_gemma":[0.0020159895,0.000601448,0.0005385538,0.0006438906,0.0010147367,0.00035196418,0.001363117,0.0009559677,0.00029687272],"study_design_candidate":"case_report","study_design_consensus":"case_report","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00040845422,0.0001291346,0.05778962,0.00006958148,0.00007187375,0.9179557,0.0010523022,0.00012499276,0.015442961,0.00060077995,0.00046961886,0.0058850143],"study_design_scores_gemma":[0.000022018847,0.00026355762,0.03544247,0.000009535622,0.000031683052,0.9608071,0.00020349788,0.00015620813,0.00236307,0.00014600578,0.0005400423,0.000014748341],"about_ca_topic_score_codex":0.003452019,"about_ca_topic_score_gemma":0.0039564986,"teacher_disagreement_score":0.003452019,"about_ca_system_score_codex":0.00058416644,"about_ca_system_score_gemma":0.00041074303,"threshold_uncertainty_score":0.006863892},"labels":[],"label_agreement":null},{"id":"W2884634246","doi":"10.1016/j.cobeha.2018.05.008","title":"Autism, psychosis, and genomic imprinting: recent discoveries and conundrums","year":2018,"lang":"en","type":"article","venue":"Current Opinion in Behavioral Sciences","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":11,"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":"Natural Sciences and Engineering Research Council of Canada","keywords":"Genomic imprinting; Autism; Imprinting (psychology); Psychosis; Offspring; Phenotype; Schizophrenia (object-oriented programming); SNP; Psychology; Biology; Gene; Genetics; Neuroscience; Developmental psychology; DNA methylation; Psychiatry; Gene expression; Single-nucleotide polymorphism; Pregnancy","score_opus":0.06942812654723494,"score_gpt":0.3792514506696602,"score_spread":0.30982332412242525,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2884634246","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":[0.005200207,0.96895254,0.0010464016,0.02243759,0.000707018,0.0000066275825,0.000048395643,0.000021921966,0.0015793272],"genre_scores_gemma":[0.030741416,0.9561417,0.001159762,0.004134145,0.007203218,0.000023778826,0.000062235005,0.000007956756,0.0005257751],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.99941814,0.00013691229,0.0000933342,0.00013005824,0.0001302058,0.00009143926],"domain_scores_gemma":[0.9949351,0.0032339075,0.0006133613,0.00021260648,0.0005761458,0.00042887198],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.003516902,0.0009489309,0.0022443186,0.0017672587,0.00058000983,0.0029965988,0.001555342,0.0030386106,0.0023322904],"category_scores_gemma":[0.0031633945,0.00035265507,0.0005747399,0.0018604746,0.0063084164,0.0062505673,0.0025659488,0.003108936,0.00044611166],"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":[0.0021866723,0.0002506247,0.015850391,0.008868084,0.0005119196,0.005965873,0.0012601126,0.0011546093,0.011261233,0.07500805,0.020719996,0.85696244],"study_design_scores_gemma":[0.00045282897,0.0013164473,0.05627672,0.00652676,0.0011285115,0.017125702,0.008095489,0.0023543122,0.004846836,0.34813523,0.5532641,0.00047704775],"about_ca_topic_score_codex":0.0012160757,"about_ca_topic_score_gemma":0.0019939116,"teacher_disagreement_score":0.003516902,"about_ca_system_score_codex":0.0011054124,"about_ca_system_score_gemma":0.0016463326,"threshold_uncertainty_score":0.018599331},"labels":[],"label_agreement":null},{"id":"W2886227808","doi":"10.1371/journal.pgen.1007587","title":"Transcription factor ASCL2 is required for development of the glycogen trophoblast cell lineage","year":2018,"lang":"en","type":"article","venue":"PLoS Genetics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":33,"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; University of British Columbia","funders":"Canadian Institutes of Health Research","keywords":"Biology; Trophoblast; Gene silencing; Genetics; Genomic imprinting; Transcription factor; Cellular differentiation; Cell biology; DNA methylation; Gene expression; Gene; Placenta","score_opus":0.02991959982545794,"score_gpt":0.24483939453820877,"score_spread":0.21491979471275083,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2886227808","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9841467,0.0011234179,0.00969116,0.00017070511,0.000047168287,0.000029006129,0.0020252904,0.0005463657,0.0022201668],"genre_scores_gemma":[0.9908687,0.00031941364,0.0026263555,0.000037739694,0.000011064805,0.000033297474,0.002335824,0.000095430216,0.0036722168],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9998497,0.000018142086,0.00001534261,0.000039656356,0.000054916858,0.000022182026],"domain_scores_gemma":[0.9998153,0.000018027737,0.000055535325,0.000021437601,0.000016840084,0.00007289775],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.000081949795,0.00051656464,0.00023286948,0.00026622214,0.00020077873,0.00028440187,0.0002382512,0.00024889273,0.0016390826],"category_scores_gemma":[0.00013297077,0.00019126838,0.00021047507,0.00016293982,0.0002967072,0.00012954927,0.0003584197,0.00039127562,0.0013963305],"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":[0.00003085992,0.0000040482955,0.00017448571,0.0000117993095,0.0000016532489,0.000101696096,0.00000594365,0.000029332947,0.999263,0.000035542253,0.000027660462,0.00031395932],"study_design_scores_gemma":[0.000016320815,0.000042045776,0.0098807635,0.000005266477,0.000010167416,0.0008664346,0.000024059145,0.001357149,0.98325527,0.00005107861,0.004484924,0.000006455774],"about_ca_topic_score_codex":0.0006501616,"about_ca_topic_score_gemma":0.00086301763,"teacher_disagreement_score":0.0016390826,"about_ca_system_score_codex":0.00040355368,"about_ca_system_score_gemma":0.00034255508,"threshold_uncertainty_score":0.00548321},"labels":[],"label_agreement":null},{"id":"W2887748933","doi":"10.1098/rsbl.2018.0523","title":"Paranoia, autism and the architecture of genomic conflicts: a reply to Abu-Akel 2018","year":2018,"lang":"en","type":"letter","venue":"Biology Letters","topic":"Genetic Syndromes and Imprinting","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":"Simon Fraser University","funders":"","keywords":"Biology; Paranoia; Autism; Architecture; Evolutionary biology; Cognitive science; Developmental psychology; Psychology; Psychiatry; Archaeology","score_opus":0.008545336770511492,"score_gpt":0.22327213291760564,"score_spread":0.21472679614709414,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2887748933","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":[0.00026802908,0.003357168,0.00006787366,0.98621964,0.009607881,0.0000029374048,0.000015398758,0.0000130446115,0.00044804157],"genre_scores_gemma":[0.007429304,0.004477334,0.00029318721,0.9165494,0.067903206,0.00002880246,0.000021294305,0.000023476068,0.0032740606],"study_design_codex":"not_applicable","study_design_gemma":"theoretical_or_conceptual","domain_scores_codex":[0.9986939,0.00053686765,0.00016073421,0.00020636282,0.00026442026,0.0001377912],"domain_scores_gemma":[0.9907631,0.006902855,0.0004906658,0.0002632708,0.0008169326,0.00076317985],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0030407538,0.00068529573,0.0014923697,0.0006558307,0.0028635536,0.0027744675,0.0020990807,0.035287675,0.0035694386],"category_scores_gemma":[0.01824518,0.000613838,0.0005499699,0.0005596933,0.0052123885,0.0060208812,0.0023832915,0.041219246,0.0025389425],"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":[0.000071854,0.000027637063,0.00065370934,0.000067300105,0.000016731852,0.0027210226,0.00031703053,0.00005793582,0.00013599366,0.005423678,0.9791214,0.011385725],"study_design_scores_gemma":[0.0001991845,0.00008210165,0.001815023,0.00045846548,0.0000454668,0.009201488,0.0014002972,0.00069002056,0.00036004317,0.039885912,0.94569576,0.0001661583],"about_ca_topic_score_codex":0.0018764937,"about_ca_topic_score_gemma":0.0034739594,"teacher_disagreement_score":0.035287675,"about_ca_system_score_codex":0.0020935775,"about_ca_system_score_gemma":0.0018971125,"threshold_uncertainty_score":0.016081274},"labels":[],"label_agreement":null},{"id":"W2889225402","doi":"10.1242/dmm.035832","title":"Fetal growth restriction in a genetic model of sporadic Beckwith–Wiedemann syndrome","year":2018,"lang":"en","type":"article","venue":"Disease Models & Mechanisms","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":7,"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":"Natural Sciences and Engineering Research Council of Canada; Canadian Institutes of Health Research; Directorate for Biological Sciences; Biotechnology and Biological Sciences Research Council; Cardiff University; Waterloo Foundation","keywords":"Beckwith–Wiedemann syndrome; Fetal growth; Fetus; Biology; Genetics; Medicine; Pregnancy; Gene; DNA methylation","score_opus":0.014868693476616793,"score_gpt":0.22317470204802578,"score_spread":0.208306008571409,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2889225402","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9867899,0.0013479894,0.005453857,0.0005798161,0.00022155284,0.0002030047,0.0012628463,0.0004125115,0.003728567],"genre_scores_gemma":[0.9824195,0.0016066266,0.008070117,0.00016594658,0.0000538686,0.0004639379,0.0009902577,0.00008732586,0.0061423844],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.999574,0.000107412416,0.000046875895,0.00010903433,0.000106725325,0.000055946766],"domain_scores_gemma":[0.9995408,0.00010318754,0.00011735635,0.00005808652,0.000016230111,0.00016436978],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00034937816,0.0010701433,0.00048032127,0.0017962586,0.0005179632,0.00042648482,0.000644343,0.0010163278,0.0028398226],"category_scores_gemma":[0.00031852446,0.0004237494,0.0004512558,0.0004162361,0.0009927091,0.00030745452,0.00061466673,0.0011787073,0.00066666293],"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":[0.0014984397,0.00089179847,0.00064188335,0.00012723327,0.000032606975,0.0027239758,0.00013896206,0.00086331856,0.9857364,0.0032466245,0.0004821051,0.0036166694],"study_design_scores_gemma":[0.0013150678,0.011446087,0.008312896,0.00020232832,0.00027244302,0.015587043,0.0004590039,0.01070358,0.91916794,0.0026975207,0.029689258,0.00014683414],"about_ca_topic_score_codex":0.0009747429,"about_ca_topic_score_gemma":0.001296318,"teacher_disagreement_score":0.0028398226,"about_ca_system_score_codex":0.0008006682,"about_ca_system_score_gemma":0.00052642386,"threshold_uncertainty_score":0.0095002055},"labels":[],"label_agreement":null},{"id":"W2889619667","doi":"10.1111/ijpo.12462","title":"Changes in cardiometabolic markers in children with Prader–Willi syndrome and nonsyndromic obesity following participation in a home‐based physical activity intervention","year":2018,"lang":"en","type":"article","venue":"Pediatric Obesity","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":14,"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":"Canadian Institutes of Health Research; U.S. Army","keywords":"Medicine; Insulin resistance; Obesity; Internal medicine; Childhood obesity; Endocrinology; Physical activity; Homeostatic model assessment; Body fat percentage; Metabolic syndrome; Body mass index; Physical therapy; Overweight","score_opus":0.007160991952919399,"score_gpt":0.25131436931593265,"score_spread":0.24415337736301326,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2889619667","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9998287,0.000051156323,0.000011373032,0.000008619351,0.0000021356173,0.000008182997,0.000022035068,0.0000014842789,0.00006627795],"genre_scores_gemma":[0.9994512,0.00008520416,0.0001320645,0.000016715185,0.0000048187876,0.000045621553,0.00014198764,0.0000010042022,0.00012137772],"study_design_codex":"observational","study_design_gemma":"nonrandomized_trial","domain_scores_codex":[0.99977666,0.00006430134,0.00001745675,0.000041457428,0.000045980658,0.000054213295],"domain_scores_gemma":[0.9995561,0.00008098225,0.00016269978,0.000016734775,0.000036516674,0.0001469933],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00035366256,0.00030951615,0.00044551157,0.00025729573,0.00020369171,0.00018947445,0.00015557789,0.00021865715,0.0008989139],"category_scores_gemma":[0.0011562901,0.00012034606,0.00028806325,0.00021418059,0.00016948897,0.0001688853,0.00023478613,0.00037803466,0.00009782757],"study_design_candidate":"nonrandomized_trial","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.004439363,0.002998255,0.9634445,0.00014001665,0.00021479918,0.0006399331,0.00069976685,0.00017322211,0.0042008143,0.0000215877,0.00034223584,0.022685569],"study_design_scores_gemma":[0.00013159,0.0027764258,0.9961035,0.000008422383,0.000034442408,0.0002660948,0.00020537208,0.000069632326,0.00026517347,0.0000040906884,0.00013200102,0.0000032336382],"about_ca_topic_score_codex":0.002747169,"about_ca_topic_score_gemma":0.004595833,"teacher_disagreement_score":0.002747169,"about_ca_system_score_codex":0.0002946311,"about_ca_system_score_gemma":0.0002718885,"threshold_uncertainty_score":0.0054623485},"labels":[],"label_agreement":null},{"id":"W2892128276","doi":"10.1002/ajmg.a.40491","title":"Dietary intake in youth with prader‐willi syndrome","year":2018,"lang":"en","type":"article","venue":"American Journal of Medical Genetics Part A","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":19,"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":"Canadian Institutes of Health Research; Women and Children's Health Research Institute; Foundation for Prader-Willi Research","keywords":"Medicine; Nutrient; Nutrient density; Obesity; Interquartile range; Food group; Micronutrient; Energy density; Vitamin; Vitamin D and neurology; Environmental health; Internal medicine; Biology","score_opus":0.015055089745961904,"score_gpt":0.2649318630061272,"score_spread":0.2498767732601653,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2892128276","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99914694,0.0003806352,0.000038543392,0.00002688213,0.0000036645515,0.000005293476,0.00018273051,0.0000026903097,0.00021256928],"genre_scores_gemma":[0.9990798,0.00036020056,0.00015051235,0.000026810023,0.000004804361,0.00001155728,0.00023553289,0.0000013652907,0.00012942535],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.999705,0.00007318141,0.000046107947,0.000067818975,0.00007335078,0.00003459721],"domain_scores_gemma":[0.9995654,0.00005866029,0.00024307963,0.000017836033,0.000052149167,0.00006280295],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00037305904,0.0002346015,0.0003981472,0.0009598438,0.00031096992,0.0003369062,0.00012214477,0.00023553544,0.0008695273],"category_scores_gemma":[0.0012066523,0.00018407886,0.00034743224,0.00078306894,0.00016094127,0.0002585802,0.0003479361,0.00027778774,0.00010863825],"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":[0.000102490405,0.000029971003,0.9963476,0.000018788223,0.000032740725,0.00013396532,0.00015116464,0.000012526724,0.00022690596,0.000012114254,0.000058765887,0.0028728964],"study_design_scores_gemma":[0.0000033302117,0.00009495811,0.99923337,0.00001279765,0.000017301667,0.00033152237,0.00013416434,0.000036773163,0.00004031238,0.000010269392,0.000083311046,0.0000019495812],"about_ca_topic_score_codex":0.005567081,"about_ca_topic_score_gemma":0.0067674047,"teacher_disagreement_score":0.005567081,"about_ca_system_score_codex":0.00023008118,"about_ca_system_score_gemma":0.00017242238,"threshold_uncertainty_score":0.011069357},"labels":[],"label_agreement":null},{"id":"W2894420738","doi":"10.1101/430694","title":"Conserved mechanism of nucleoporin regulation of the <i>Kcnq1ot1</i> imprinted domain with divergence in embryonic and trophoblast stem cells","year":2018,"lang":"en","type":"preprint","venue":"bioRxiv (Cold Spring Harbor Laboratory)","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":0,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Lawson Health Research Institute; Western University","funders":"Canadian Institutes of Health Research; Magee-Womens Research Institute; University of Pittsburgh","keywords":"Nucleoporin; Biology; CTCF; Cell biology; Genomic imprinting; Embryonic stem cell; Genetics; DNA methylation; Gene; Cell nucleus; Gene expression; Nuclear transport","score_opus":0.006623870198471408,"score_gpt":0.18194872419563224,"score_spread":0.17532485399716083,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2894420738","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99568415,0.0005761239,0.0027487183,0.000037627695,0.000005509079,0.00000711207,0.00014372786,0.00004302618,0.00075406325],"genre_scores_gemma":[0.99819905,0.0001399486,0.00069415354,0.000016226171,0.0000016372402,0.0000068786576,0.0001705924,0.000011307025,0.00076029653],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9998951,0.0000107133965,0.00000946078,0.000030232028,0.000037124057,0.00001750458],"domain_scores_gemma":[0.9998512,0.000017558034,0.000059073573,0.000015820786,0.000017001996,0.000039156894],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00009607941,0.00019138039,0.00015842836,0.00013793806,0.0001229301,0.00026791517,0.00021885199,0.00020131354,0.00056432985],"category_scores_gemma":[0.000084603285,0.00011579042,0.00013774286,0.00006144729,0.00022338996,0.00015039637,0.0002701369,0.00029418032,0.00018628652],"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":[0.000013699928,0.0000012666006,0.00038379882,0.000009483773,0.000001571237,0.000031455533,0.000010270563,0.000022823951,0.9991385,0.00010447688,0.0000048301877,0.0002779153],"study_design_scores_gemma":[0.0000054056813,0.000041050695,0.029053759,0.000004555376,0.000011353797,0.00047291187,0.000039628576,0.0009172004,0.9678916,0.00008587449,0.0014725795,0.0000040497807],"about_ca_topic_score_codex":0.00045911572,"about_ca_topic_score_gemma":0.00061501155,"teacher_disagreement_score":0.00056432985,"about_ca_system_score_codex":0.00029925664,"about_ca_system_score_gemma":0.00014803708,"threshold_uncertainty_score":0.002171278},"labels":[],"label_agreement":null},{"id":"W2894978875","doi":"10.1016/j.jcjd.2018.08.097","title":"Fetal Serum Phosphorus is Set Independently of Maternal Serum Phosphorus and Phosphorus Intake","year":2018,"lang":"en","type":"article","venue":"Canadian Journal of Diabetes","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":0,"is_retracted":false,"has_abstract":false,"route_ca_aff":false,"route_ca_fund":false,"route_ca_venue":true,"route_about_ca":false,"ca_institutions":"","funders":"","keywords":"Phosphorus; Endocrinology; Parathyroid hormone; Fetus; Medicine; Phosphorus deficiency; Internal medicine; Black phosphorus; Calcium; Pregnancy; Biology; Chemistry","score_opus":0.007867445049499868,"score_gpt":0.2129977249535344,"score_spread":0.2051302799040345,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2894978875","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9833878,0.0018826938,0.0057864347,0.000577093,0.00008517794,0.000013525713,0.000924462,0.00025895622,0.0070837787],"genre_scores_gemma":[0.99580413,0.00055062183,0.0014680352,0.000052980293,0.000019300895,0.000013470251,0.00026269135,0.00006896015,0.0017597666],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.99932635,0.00013441018,0.000034768105,0.0001235865,0.0002815442,0.00009935466],"domain_scores_gemma":[0.99792755,0.0009979211,0.0003568523,0.00014049068,0.00018371556,0.0003934706],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00052167306,0.00049602886,0.00068526407,0.0012335083,0.00037733582,0.0012889446,0.0006408704,0.0005159744,0.0016540595],"category_scores_gemma":[0.0028742673,0.0005783585,0.00029987012,0.0006166682,0.00087325874,0.0004236884,0.00072907005,0.00068648905,0.0003334844],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0061209626,0.00010796024,0.13114804,0.00012684726,0.0001886505,0.0039705127,0.0007142433,0.0015275046,0.81362224,0.004728317,0.0008776624,0.036867093],"study_design_scores_gemma":[0.00014005839,0.00032383716,0.8326415,0.00004560836,0.00018445334,0.0031287302,0.0003357904,0.004208088,0.15298128,0.0032528683,0.002642123,0.00011567534],"about_ca_topic_score_codex":0.017075734,"about_ca_topic_score_gemma":0.013719249,"teacher_disagreement_score":0.017075734,"about_ca_system_score_codex":0.0011949543,"about_ca_system_score_gemma":0.0014747088,"threshold_uncertainty_score":0.033952713},"labels":[],"label_agreement":null},{"id":"W2897168131","doi":"10.7554/elife.42368","title":"The discovery and importance of genomic imprinting","year":2018,"lang":"en","type":"article","venue":"eLife","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":75,"is_retracted":false,"has_abstract":true,"route_ca_aff":false,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":true,"ca_institutions":"","funders":"","keywords":"Genomic imprinting; Epigenetics; Biology; Imprinting (psychology); Genetics; Gene; DNA methylation; Gene expression","score_opus":0.006511186296832042,"score_gpt":0.23186166614246737,"score_spread":0.22535047984563533,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2897168131","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":[0.104299925,0.6671675,0.03784679,0.11855893,0.014361549,0.000029662602,0.0006858624,0.0004915205,0.056558322],"genre_scores_gemma":[0.5046616,0.43597823,0.013059721,0.016095761,0.008310914,0.000054105785,0.0004712449,0.00014630995,0.021222044],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.9995714,0.00008786576,0.00001853224,0.000111315785,0.00014331283,0.000067546505],"domain_scores_gemma":[0.99893063,0.00053636334,0.00006282883,0.00013234674,0.00018683917,0.00015088146],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0017113099,0.00030495037,0.00034180185,0.000629013,0.0005037988,0.001456631,0.00046783616,0.0008891256,0.0011430717],"category_scores_gemma":[0.002476671,0.00023570009,0.00021499144,0.00046779844,0.003207649,0.002297042,0.0013589897,0.0036907098,0.0006392231],"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":[0.00041831005,0.000064924185,0.0037436415,0.0007704627,0.00008010004,0.0015447479,0.00088665425,0.001425473,0.08607907,0.41859004,0.04450369,0.44189286],"study_design_scores_gemma":[0.00003588034,0.0001276217,0.0036750142,0.0002120829,0.00003708121,0.0015837786,0.00032759417,0.0009300109,0.074958675,0.1338286,0.78420275,0.00008093845],"about_ca_topic_score_codex":0.0009618249,"about_ca_topic_score_gemma":0.00077370554,"teacher_disagreement_score":0.0017113099,"about_ca_system_score_codex":0.0010456912,"about_ca_system_score_gemma":0.0009483028,"threshold_uncertainty_score":0.009050369},"labels":[],"label_agreement":null},{"id":"W2898659056","doi":"10.1016/j.transci.2018.10.008","title":"Introduction to part two of a three-part theme on hereditary bleeding disorders","year":2018,"lang":"en","type":"editorial","venue":"Transfusion and Apheresis Science","topic":"Genetic Syndromes and Imprinting","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":"Memorial University of Newfoundland","funders":"","keywords":"Medicine; Wish; Associate editor; Hemostasis; Hematologist; Library science; Internal medicine; Sociology; Computer science","score_opus":0.008644078713782387,"score_gpt":0.25106347197528345,"score_spread":0.24241939326150105,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2898659056","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":[0.000020733867,0.005924645,0.00009149093,0.024764152,0.968567,0.000010540191,0.000023251543,0.000020557356,0.0005776378],"genre_scores_gemma":[0.00018839426,0.0031371526,0.000075372984,0.027138125,0.96625906,0.000022422002,0.000024749284,0.000023820434,0.003130961],"study_design_codex":"not_applicable","study_design_gemma":"not_applicable","domain_scores_codex":[0.9946806,0.0011198284,0.0007602896,0.0007504036,0.0021963106,0.00049247785],"domain_scores_gemma":[0.9754964,0.011765451,0.0021152229,0.0006485245,0.0061193923,0.0038549644],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.007475477,0.003948029,0.0041390713,0.0050264844,0.003186902,0.00770114,0.0035843945,0.015721459,0.020190975],"category_scores_gemma":[0.02393857,0.0011089921,0.0032406992,0.0019920412,0.0030112353,0.0044172397,0.003817095,0.024562214,0.008059571],"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":[0.0000440084,0.000012729086,0.000030698768,0.00023579161,0.000023417218,0.00010401327,0.000013871689,0.000017669165,0.00007261552,0.00025317573,0.9947523,0.004439618],"study_design_scores_gemma":[0.00012935308,0.00005299671,0.00033185424,0.000884244,0.00010166411,0.00033794282,0.000044441003,0.00012908947,0.00012306732,0.0011298254,0.9967077,0.000027791855],"about_ca_topic_score_codex":0.0011090655,"about_ca_topic_score_gemma":0.0033966412,"teacher_disagreement_score":0.020190975,"about_ca_system_score_codex":0.0034902073,"about_ca_system_score_gemma":0.0037257473,"threshold_uncertainty_score":0.06754559},"labels":[],"label_agreement":null},{"id":"W2899340054","doi":"10.1210/jc.2018-01504","title":"Hypermethylator Phenotype and Ectopic GIP Receptor in GNAS Mutation-Negative Somatotropinomas","year":2018,"lang":"en","type":"article","venue":"The Journal of Clinical Endocrinology & Metabolism","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","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; Centre Hospitalier de l’Université de Montréal","funders":"Fondation pour la Recherche Médicale","keywords":"Acromegaly; GNAS complex locus; Gigantism; Biology; Endocrinology; Internal medicine; Ectopic expression; Phenotype; Allele; Somatotropic cell; DNA methylation; Gene expression; Genetics; Gene; Pituitary gland; Hormone; Medicine; Growth hormone","score_opus":0.027076818027284785,"score_gpt":0.33598587923603895,"score_spread":0.30890906120875417,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2899340054","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99947184,0.000074976,0.00027626712,0.000010437035,9.1761024e-7,0.0000034475245,0.000023630659,0.000009665059,0.00012881818],"genre_scores_gemma":[0.99958473,0.0000316251,0.0002897899,0.000007253711,0.000002607444,0.000003565527,0.000034336215,0.0000027608917,0.000043354616],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.99989605,0.0000148011895,0.000010946047,0.000034245582,0.000027042164,0.000016816086],"domain_scores_gemma":[0.9998252,0.00005593191,0.0000606819,0.00001492063,0.000013589548,0.000029698753],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00014403074,0.00029860143,0.00016789367,0.0004831073,0.0001785944,0.00018509792,0.00013484572,0.00025921236,0.0011600847],"category_scores_gemma":[0.00048447464,0.0001234911,0.00010938293,0.00023163385,0.00040605525,0.00010639021,0.00022908805,0.00016977346,0.0001520613],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.000752814,0.000026323416,0.33512962,0.00009128777,0.000041725805,0.016809147,0.0003880896,0.00025441963,0.64048296,0.00009725534,0.00008057916,0.0058459234],"study_design_scores_gemma":[0.000043618154,0.00050254224,0.814921,0.000008799106,0.00007452333,0.10882574,0.00037704493,0.0012529365,0.073166326,0.00018964977,0.0006236416,0.000014188183],"about_ca_topic_score_codex":0.00041443814,"about_ca_topic_score_gemma":0.00055232283,"teacher_disagreement_score":0.0011600847,"about_ca_system_score_codex":0.00016158832,"about_ca_system_score_gemma":0.00011948482,"threshold_uncertainty_score":0.0038808584},"labels":[],"label_agreement":null},{"id":"W2908470212","doi":"10.1101/gad.320069.118","title":"ZNF445 is a primary regulator of genomic imprinting","year":2019,"lang":"en","type":"article","venue":"Genes & Development","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":224,"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":"H2020 European Research Council; Medical Research Council; Medical Research Council Canada; European Commission; Wellcome Trust; Gebert Rüf Stiftung; Schweizerischer Nationalfonds zur Förderung der Wissenschaftlichen Forschung; National Science Foundation","keywords":"Biology; Genomic imprinting; Imprinting (psychology); Reprogramming; Epigenetics; DNA methylation; Penetrance; Genetics; Regulator; Regulation of gene expression; Zinc finger; Gene; Phenotype; Gene expression; Cell biology; Transcription factor","score_opus":0.005898302427109366,"score_gpt":0.20275046994225154,"score_spread":0.19685216751514217,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2908470212","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9853892,0.0032952018,0.0072375108,0.00013181384,0.000038591366,0.00001625663,0.00069324387,0.00023239017,0.0029657877],"genre_scores_gemma":[0.9930275,0.00061779865,0.0021557491,0.00003369306,0.0000077488785,0.000006057938,0.00063669466,0.000009359322,0.0035053992],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9999398,0.000003602229,0.00000293877,0.000021932769,0.00002075452,0.000010946578],"domain_scores_gemma":[0.9999615,0.000002520785,0.000015535075,0.0000025345012,0.0000029379594,0.000014942815],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.000045380555,0.0002736069,0.00014355866,0.00019277944,0.00019966002,0.0001994412,0.00021038738,0.00018525135,0.0010906543],"category_scores_gemma":[0.000077678276,0.000087367254,0.00013201844,0.00010786632,0.00014140205,0.00007761881,0.0001618463,0.00014700992,0.0003841591],"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":[0.00010458335,0.00001331124,0.0020094984,0.00003150766,0.000009170738,0.00025039597,0.000009068288,0.000113641036,0.9875585,0.00039543735,0.00017831451,0.009326592],"study_design_scores_gemma":[0.000017448268,0.00014588442,0.041637484,0.000007617875,0.000023950244,0.0019359898,0.000018832172,0.0011182093,0.94074005,0.00023476603,0.014112445,0.000007250403],"about_ca_topic_score_codex":0.00096984894,"about_ca_topic_score_gemma":0.0012098454,"teacher_disagreement_score":0.0010906543,"about_ca_system_score_codex":0.0002449415,"about_ca_system_score_gemma":0.00018666932,"threshold_uncertainty_score":0.0036485791},"labels":[],"label_agreement":null},{"id":"W2908503642","doi":"10.1111/cge.13151","title":"Are all Xq26.2 duplications overlapping <i>GPC3</i> on array‐CGH a cause of Simpson‐Golabi‐Behmel syndrome? When do we need transcript analysis?","year":2018,"lang":"en","type":"letter","venue":"Clinical Genetics","topic":"Genetic Syndromes and Imprinting","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":"Centre Hospitalier Universitaire Sainte-Justine","funders":"","keywords":"Genetics; Biology; Gene duplication; Gene","score_opus":0.06180763596712226,"score_gpt":0.33024938877234566,"score_spread":0.2684417528052234,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2908503642","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":[0.0072484454,0.0027540952,0.00044187726,0.97609556,0.008796206,0.000016304508,0.00013518814,0.00007270069,0.0044396166],"genre_scores_gemma":[0.13762248,0.009903044,0.0027564722,0.73605895,0.0968873,0.00008259213,0.00026510487,0.0001265083,0.016297525],"study_design_codex":"not_applicable","study_design_gemma":"observational","domain_scores_codex":[0.9993857,0.00014637169,0.00009531357,0.00010641223,0.00015441999,0.0001117502],"domain_scores_gemma":[0.9975898,0.0013594507,0.00018710906,0.00010117389,0.00044089174,0.0003216462],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0008025137,0.00047885656,0.0008366669,0.00057344657,0.0013141099,0.0010844552,0.0010649647,0.015578074,0.0043004844],"category_scores_gemma":[0.008353534,0.00035292175,0.0005254386,0.00042771787,0.0012311677,0.0020237928,0.00059934333,0.009760887,0.0036965183],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00029736265,0.000099531564,0.012141089,0.00014880537,0.00005077673,0.18870433,0.00042748614,0.0004434093,0.002601248,0.006516474,0.73407066,0.054498788],"study_design_scores_gemma":[0.00040227358,0.00026421843,0.011088274,0.00049795763,0.00011288256,0.3153513,0.0015987387,0.0028498261,0.0023368306,0.041145165,0.6242083,0.00014424961],"about_ca_topic_score_codex":0.0022957756,"about_ca_topic_score_gemma":0.0026306005,"teacher_disagreement_score":0.015578074,"about_ca_system_score_codex":0.0016084205,"about_ca_system_score_gemma":0.0008143178,"threshold_uncertainty_score":0.014386535},"labels":[],"label_agreement":null},{"id":"W2908505564","doi":"10.1111/ijpo.12493","title":"Obestatin and adropin in Prader‐Willi syndrome and nonsyndromic obesity: Associations with weight, BMI‐z, and HOMA‐IR","year":2018,"lang":"en","type":"article","venue":"Pediatric Obesity","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":13,"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":"Eunice Kennedy Shriver National Institute of Child Health and Human Development; Canadian Institutes of Health Research","keywords":"Obestatin; Ghrelin; Medicine; Endocrinology; Internal medicine; Obesity; Childhood obesity; Hormone; Overweight","score_opus":0.005525405858576366,"score_gpt":0.21257506939000162,"score_spread":0.20704966353142526,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2908505564","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9996866,0.00017412823,0.00003566491,0.0000044911835,0.0000013703202,0.0000015411479,0.0000311301,9.2374523e-7,0.00006427556],"genre_scores_gemma":[0.99950933,0.00014849332,0.00014447237,0.0000056033196,0.0000044627527,0.0000053933227,0.00008428679,0.0000014583228,0.00009655901],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9998216,0.00003525692,0.00002770347,0.00004801356,0.000041185052,0.000026229141],"domain_scores_gemma":[0.99941325,0.00013573104,0.000269963,0.000030402629,0.00002991781,0.000120752324],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00032377275,0.00040434135,0.00029390614,0.00089711446,0.0001509056,0.00034026807,0.00017334585,0.000313918,0.0009798389],"category_scores_gemma":[0.0009499133,0.00026416554,0.00027470678,0.0005525105,0.00032758803,0.00034539428,0.0003826184,0.00041281266,0.00012926312],"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":[0.0008710521,0.00007107923,0.98612636,0.00002623081,0.00008192327,0.0004587787,0.00013927392,0.000066070024,0.008165058,0.000033810335,0.000027345974,0.0039328756],"study_design_scores_gemma":[0.000006886152,0.00017906132,0.9985617,0.0000021232465,0.000014417327,0.00063790655,0.000052976535,0.00006891681,0.0003967829,0.000011872667,0.00006541267,0.0000019853767],"about_ca_topic_score_codex":0.0011285825,"about_ca_topic_score_gemma":0.0013338507,"teacher_disagreement_score":0.0011285825,"about_ca_system_score_codex":0.00015473976,"about_ca_system_score_gemma":0.00013640705,"threshold_uncertainty_score":0.0032778978},"labels":[],"label_agreement":null},{"id":"W2910777113","doi":"10.1111/cen.13933","title":"Hormonal and metabolic effects of carbohydrate restriction in children with Prader‐Willi syndrome","year":2019,"lang":"en","type":"article","venue":"Clinical Endocrinology","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","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":"University of Alberta Hospital; University of Alberta","funders":"Eunice Kennedy Shriver National Institute of Child Health and Human Development; National Institute of Child Health and Human Development; Foundation for Prader-Willi Research","keywords":"Postprandial; Internal medicine; Endocrinology; Carbohydrate; Ghrelin; Adiponectin; Insulin; Calorie; Meal; Glucagon-like peptide-1; Medicine; Hormone; Insulin resistance; Type 2 diabetes; Diabetes mellitus","score_opus":0.007751614674323291,"score_gpt":0.25926566326243433,"score_spread":0.25151404858811105,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2910777113","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9997551,0.00008935384,0.000021030679,0.000014063277,0.0000023752907,0.0000030161202,0.000044216526,0.0000020253483,0.00006886848],"genre_scores_gemma":[0.99952424,0.00013196535,0.00011917189,0.000015674224,0.0000059801755,0.0000096951635,0.00011855557,0.0000013748895,0.00007336718],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99980754,0.000056521392,0.000016583965,0.000045509692,0.000039972256,0.000033942586],"domain_scores_gemma":[0.99956983,0.000116385396,0.00018154392,0.000019556323,0.000020087464,0.0000924628],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00021979342,0.00044126261,0.00039018632,0.00035729186,0.00021826517,0.00023202132,0.00015013544,0.00020973086,0.001204859],"category_scores_gemma":[0.0010836172,0.00016059236,0.0002563078,0.000336089,0.0003507849,0.00018401691,0.00029259463,0.00038025592,0.0001049369],"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":[0.0019713624,0.00025533876,0.978815,0.000056328376,0.0001003044,0.0026056515,0.000244255,0.00013975246,0.009150365,0.000038010996,0.00011649271,0.0065071867],"study_design_scores_gemma":[0.00004633955,0.0010332576,0.99533266,0.0000072991775,0.000029192757,0.0027205623,0.00019461884,0.00008433456,0.00038259168,0.000014357706,0.0001510481,0.000003812349],"about_ca_topic_score_codex":0.0017064176,"about_ca_topic_score_gemma":0.0019318443,"teacher_disagreement_score":0.0017064176,"about_ca_system_score_codex":0.00019816154,"about_ca_system_score_gemma":0.00018343776,"threshold_uncertainty_score":0.004030645},"labels":[],"label_agreement":null},{"id":"W2914071115","doi":"10.1177/2050312118823585","title":"Baby food and bedtime: Evidence for opposite phenotypes from different genetic and epigenetic alterations in Prader-Willi and Angelman syndromes","year":2019,"lang":"en","type":"review","venue":"SAGE Open Medicine","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":15,"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":"Canadian Network for Research and Innovation in Machining Technology, Natural Sciences and Engineering Research Council of Canada","keywords":"Angelman syndrome; UBE3A; Genomic imprinting; Rett syndrome; Neurodevelopmental disorder; Phenotype; Epigenetics; MECP2; Medicine; Chromosome 15; Genetics; Endocrinology; Gene; Biology; DNA methylation; Chromosome; Gene expression","score_opus":0.10410958322111684,"score_gpt":0.3669626128591385,"score_spread":0.26285302963802165,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2914071115","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":[0.9351598,0.056839917,0.0031632225,0.0007896568,0.00013089603,0.000028577933,0.0022820295,0.00004212109,0.001563818],"genre_scores_gemma":[0.9918133,0.005494745,0.0011482006,0.00032178813,0.00005558953,0.00002049953,0.0009148359,0.000025710013,0.00020538188],"study_design_codex":"observational","study_design_gemma":"systematic_review","domain_scores_codex":[0.99816906,0.0004866656,0.00021653154,0.0008388848,0.00022741206,0.00006141557],"domain_scores_gemma":[0.9969598,0.0015909915,0.0009643141,0.00022353558,0.00013898795,0.00012242317],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.001643314,0.0008604546,0.00081640895,0.0008958205,0.00021895592,0.0006337016,0.00058769726,0.00062606257,0.0023287858],"category_scores_gemma":[0.0041515273,0.00030216284,0.0023587965,0.0011089747,0.0007535029,0.0003920272,0.00058898114,0.0005695802,0.00010966345],"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":[0.005897601,0.00009720737,0.89530635,0.0031289964,0.03645756,0.0016137573,0.00046947188,0.0005939369,0.024656609,0.0016151761,0.0006741373,0.029489273],"study_design_scores_gemma":[0.00025240134,0.00039216244,0.9756551,0.00024775846,0.01497498,0.0018749784,0.0001525975,0.0006378684,0.0023560207,0.0014858004,0.0019329014,0.00003749086],"about_ca_topic_score_codex":0.002456275,"about_ca_topic_score_gemma":0.0033830034,"teacher_disagreement_score":0.002456275,"about_ca_system_score_codex":0.0002869742,"about_ca_system_score_gemma":0.0002544357,"threshold_uncertainty_score":0.008690774},"labels":[],"label_agreement":null},{"id":"W2915087909","doi":"10.1101/560474","title":"BORIS/CTCFL promotes a switch from a proliferative towards an invasive phenotype in melanoma cell lines","year":2019,"lang":"en","type":"preprint","venue":"bioRxiv (Cold Spring Harbor Laboratory)","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":0,"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; Jewish General Hospital","funders":"Canadian Institutes of Health Research; McGill University; Israel Cancer Research Fund","keywords":"Reprogramming; Melanoma; Phenotype; Biology; Cancer research; Transcriptome; Phenotypic switching; Regulator; Transcriptional regulation; Cell; Transcription factor; Gene expression; Genetics; Gene","score_opus":0.011951469963488203,"score_gpt":0.22359190229947656,"score_spread":0.21164043233598837,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2915087909","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9922093,0.00047532475,0.0026510765,0.000094299154,0.000028826065,0.00002560691,0.0012067534,0.00018346333,0.0031253106],"genre_scores_gemma":[0.9893656,0.00026127283,0.0019411454,0.000058251437,0.0000067520245,0.000028218808,0.0018570896,0.000047193655,0.006434566],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9999058,0.000013298601,0.000008808292,0.000019668178,0.00003084363,0.00002145568],"domain_scores_gemma":[0.99993694,0.000017066326,0.000010352839,0.000013154071,0.0000064267715,0.000016046004],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00009879927,0.00017098345,0.00013871427,0.00018236121,0.00012071154,0.00019143459,0.00010331637,0.000156421,0.0020442905],"category_scores_gemma":[0.000052352818,0.00011433086,0.00014292463,0.0001229947,0.00011681325,0.00007891091,0.00014558647,0.00040212434,0.0005362508],"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":[0.000026610205,0.000012719468,0.00009351601,0.000007736762,0.0000014657977,0.000019998686,0.0000070299266,0.000029218572,0.99942636,0.000045949255,0.00004493019,0.00028461256],"study_design_scores_gemma":[0.000008055184,0.00010024595,0.0033933697,0.000001948219,0.0000036942154,0.000069162415,0.000017522905,0.000763486,0.9938923,0.000033896842,0.0017140527,0.0000023551272],"about_ca_topic_score_codex":0.0009958185,"about_ca_topic_score_gemma":0.0011014332,"teacher_disagreement_score":0.0020442905,"about_ca_system_score_codex":0.00018802551,"about_ca_system_score_gemma":0.00009506137,"threshold_uncertainty_score":0.006838858},"labels":[],"label_agreement":null},{"id":"W2917246659","doi":"10.1002/ajmg.a.61071","title":"Disruption of the PTHLH regulatory landscape results in features consistent with hyperparathyroid disease","year":2019,"lang":"en","type":"article","venue":"American Journal of Medical Genetics Part A","topic":"Genetic Syndromes and Imprinting","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; Hospital for Sick Children; University of Toronto","funders":"Science and Engineering Research Board","keywords":"Enhancer; Regulatory sequence; Parathyroid hormone; Coding region; Cancer research; Biology; Transcription factor; Medicine; Endocrinology; Internal medicine; Genetics; Gene","score_opus":0.005481013258852192,"score_gpt":0.23679842735114648,"score_spread":0.23131741409229428,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2917246659","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9967823,0.00030742254,0.0009345541,0.00013289331,0.000012527339,0.000010170551,0.00013178018,0.000052574636,0.0016357322],"genre_scores_gemma":[0.9988355,0.00015087919,0.00047486456,0.00003416456,0.000013534638,0.0000028068462,0.000050897135,0.000008820102,0.00042838295],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9998196,0.000022066875,0.000016893817,0.00005782368,0.000050612354,0.00003298004],"domain_scores_gemma":[0.9998073,0.000057802514,0.00006402818,0.000010721757,0.000008152467,0.00005214731],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.000094506766,0.0005717392,0.00026193596,0.00058791274,0.00026350576,0.00030725027,0.00023028791,0.0006123468,0.0017243252],"category_scores_gemma":[0.00045181817,0.00017168185,0.00014428243,0.0003280853,0.0005918282,0.00018141913,0.00031741406,0.00036782195,0.000267376],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00039764194,0.00007680872,0.037041754,0.00007618265,0.000041275154,0.24986778,0.00039185077,0.00043617937,0.70169246,0.0012138125,0.00037931427,0.008384893],"study_design_scores_gemma":[0.000050421648,0.00036782844,0.14446332,0.000017811844,0.00008562798,0.729287,0.0002975615,0.0011010345,0.12043531,0.00076184346,0.0031060171,0.000026224348],"about_ca_topic_score_codex":0.0003113449,"about_ca_topic_score_gemma":0.00049228227,"teacher_disagreement_score":0.0017243252,"about_ca_system_score_codex":0.00017003107,"about_ca_system_score_gemma":0.0001421098,"threshold_uncertainty_score":0.005768478},"labels":[],"label_agreement":null},{"id":"W2922146825","doi":"10.1016/j.psychres.2019.03.019","title":"Genetic variation of UBE3A is associated with schizotypy in a population of typical individuals","year":2019,"lang":"en","type":"article","venue":"Psychiatry Research","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":8,"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; Simon Fraser University","funders":"Natural Sciences and Engineering Research Council of Canada","keywords":"UBE3A; Angelman syndrome; Psychosis; Genetics; Schizotypy; Biology; Autism; Population; Schizophrenia (object-oriented programming); Haplotype; Penetrance; Genotype; Psychology; Phenotype; Medicine; Psychiatry; Gene","score_opus":0.02140425203211636,"score_gpt":0.31709655928177666,"score_spread":0.2956923072496603,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2922146825","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9996189,0.000028438748,0.000066001994,0.000017214234,0.0000035360727,0.0000035553028,0.00006473095,0.0000024487401,0.00019516879],"genre_scores_gemma":[0.99948967,0.000035511315,0.00012615707,0.000015536692,0.000005547487,0.000004789649,0.00009876821,0.0000038415806,0.0002200766],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9995346,0.00013114959,0.000046290716,0.00013213902,0.000083032646,0.00007278498],"domain_scores_gemma":[0.9994436,0.00013177902,0.00018447978,0.00005124803,0.000049908183,0.00013900359],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0002781134,0.00089373725,0.0004925233,0.0019173075,0.0015716703,0.0006490199,0.00034224318,0.00044122897,0.0026682308],"category_scores_gemma":[0.0014187618,0.00032411155,0.0005142387,0.0012761002,0.0006776258,0.0002446936,0.00073532824,0.0005210119,0.0002210675],"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":[0.0017139514,0.0002373626,0.954162,0.00002527426,0.00031945776,0.005146956,0.002370182,0.00013891794,0.03048007,0.00032657097,0.0002521231,0.0048270854],"study_design_scores_gemma":[0.000019653504,0.00023080439,0.9948147,0.0000066889106,0.0000600856,0.0032297084,0.0006947803,0.00019305057,0.00045114127,0.00012227656,0.0001637674,0.000013258236],"about_ca_topic_score_codex":0.007055606,"about_ca_topic_score_gemma":0.0062366733,"teacher_disagreement_score":0.007055606,"about_ca_system_score_codex":0.00030122718,"about_ca_system_score_gemma":0.00020899744,"threshold_uncertainty_score":0.014029086},"labels":[],"label_agreement":null},{"id":"W2922220912","doi":"10.1016/j.omtm.2019.03.001","title":"Preclinical Testing in Translational Animal Models of Prader-Willi Syndrome: Overview and Gap Analysis","year":2019,"lang":"en","type":"review","venue":"Molecular Therapy — Methods & Clinical Development","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","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":"University of Alberta","funders":"Canadian Institutes of Health Research","keywords":"Endophenotype; Medicine; Clinical trial; Context (archaeology); Bioinformatics; Translational research; Disease; Preclinical research; Neuroscience; Biology; Internal medicine; Pathology; Cognition; Psychiatry","score_opus":0.39317348149902526,"score_gpt":0.51069152147912,"score_spread":0.11751803998009475,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2922220912","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":[0.0003060882,0.9967907,0.00048161182,0.00031126646,0.00013962392,0.000034273988,0.000086205735,0.00001866605,0.0018315748],"genre_scores_gemma":[0.0012220377,0.9968682,0.0007156343,0.00023634093,0.000065874876,0.000040300005,0.000104540435,0.000004802503,0.00074226514],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.9996978,0.000078093,0.000048572398,0.000042775686,0.00010844435,0.00002431045],"domain_scores_gemma":[0.9990627,0.0006107557,0.0000967743,0.000031770178,0.00015748067,0.00004049123],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.001733575,0.0008915038,0.0016559779,0.002552267,0.00019642316,0.0009658544,0.0011000783,0.0012925146,0.003821222],"category_scores_gemma":[0.0012151385,0.00033116748,0.0008738455,0.0012942399,0.0005048205,0.0010137656,0.0006602262,0.001960106,0.0019858312],"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":[0.00017879363,0.00013673486,0.0001388591,0.02666045,0.00015453303,0.00019523315,0.000045641336,0.00031232013,0.0043775463,0.005997502,0.014422627,0.94737977],"study_design_scores_gemma":[0.000081123515,0.00044429177,0.0009938149,0.0088145835,0.00045043914,0.0012340785,0.000058586196,0.000113871414,0.0032301855,0.003145532,0.9813983,0.000035086658],"about_ca_topic_score_codex":0.0008018837,"about_ca_topic_score_gemma":0.0017079001,"teacher_disagreement_score":0.003821222,"about_ca_system_score_codex":0.00060976157,"about_ca_system_score_gemma":0.0012652031,"threshold_uncertainty_score":0.012783289},"labels":[],"label_agreement":null},{"id":"W2923698345","doi":"","title":"Kane and Able","year":2017,"lang":"en","type":"article","venue":"Dalhousie review","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":0,"is_retracted":false,"has_abstract":false,"route_ca_aff":false,"route_ca_fund":false,"route_ca_venue":true,"route_about_ca":false,"ca_institutions":"","funders":"","keywords":"Geology","score_opus":0.0179352793432706,"score_gpt":0.28720217669327835,"score_spread":0.26926689735000775,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2923698345","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":[0.0016653257,0.42178184,0.008027483,0.0573152,0.036074337,0.0001361417,0.00062463206,0.00046474705,0.47391027],"genre_scores_gemma":[0.015767727,0.2673147,0.0056623137,0.019981608,0.007551811,0.00015454274,0.00062093796,0.00021637559,0.68273],"study_design_codex":"not_applicable","study_design_gemma":"not_applicable","domain_scores_codex":[0.99938655,0.00009855451,0.000045592245,0.00012185466,0.0002517945,0.0000955152],"domain_scores_gemma":[0.9994974,0.0001167321,0.000018598146,0.00007649639,0.00016955273,0.000121198835],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00095263956,0.0007754756,0.00054329564,0.0026887155,0.0010201542,0.002396853,0.001097308,0.002218067,0.076900765],"category_scores_gemma":[0.002974625,0.0002889236,0.00045883635,0.001308392,0.0013723178,0.0022827336,0.0035443453,0.0024835356,0.03582327],"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":[0.00005067554,0.00003229521,0.00039645052,0.00047022905,0.000012599484,0.0009764567,0.0002609663,0.00006449554,0.0007201286,0.03297354,0.57440066,0.38964143],"study_design_scores_gemma":[0.0000030362364,0.000003912266,0.000114494884,0.00013579096,0.0000028871102,0.0008545456,0.000037382786,0.0000064326177,0.00009232804,0.0011147896,0.9976305,0.0000039589754],"about_ca_topic_score_codex":0.0026595097,"about_ca_topic_score_gemma":0.0058362773,"teacher_disagreement_score":0.076900765,"about_ca_system_score_codex":0.00094915606,"about_ca_system_score_gemma":0.0023982283,"threshold_uncertainty_score":0.2572587},"labels":[],"label_agreement":null},{"id":"W2944830605","doi":"10.1080/17518423.2019.1619857","title":"Using Behavioral Approaches to Assess Memory, Imitation and Motor Performance in Children with Angelman Syndrome: Results of a Pilot Study","year":2019,"lang":"en","type":"article","venue":"Developmental Neurorehabilitation","topic":"Genetic Syndromes and Imprinting","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":"University of Toronto; Hospital for Sick Children","funders":"Angelman Syndrome Foundation","keywords":"Angelman syndrome; Psychology; Imitation; Developmental psychology; Physical medicine and rehabilitation; Clinical psychology; Cognitive psychology; Medicine; Neuroscience","score_opus":0.0843971213659254,"score_gpt":0.2692353614891771,"score_spread":0.18483824012325167,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2944830605","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99969625,0.000038715156,0.0000939691,0.0000056264794,0.0000014028996,0.000021385065,0.00004020076,0.0000030204476,0.000099428406],"genre_scores_gemma":[0.9989518,0.000086356056,0.00059325225,0.000011376459,0.0000024594428,0.00006234657,0.00016474734,0.0000025659053,0.00012500848],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99928147,0.00027812136,0.000094767354,0.000107082764,0.00014315,0.00009531235],"domain_scores_gemma":[0.9987955,0.00036607374,0.00031405673,0.000111841415,0.00024356344,0.00016881255],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0013557218,0.0008605706,0.00039288992,0.00064290455,0.00032470352,0.0002634922,0.00033321363,0.0003459459,0.0004822706],"category_scores_gemma":[0.0025832548,0.00017349253,0.0005532227,0.00031917318,0.00063919753,0.0004095167,0.00040752476,0.0005227734,0.00021268244],"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":[0.0008517582,0.0017763224,0.969016,0.00008476809,0.000114473216,0.001289473,0.0017859809,0.000253297,0.01040295,0.000018462095,0.00009228072,0.014314217],"study_design_scores_gemma":[0.00007257427,0.006063088,0.986839,0.00000990338,0.000056769186,0.0019342385,0.00091427314,0.00020638063,0.0035889477,0.000016455346,0.00028705242,0.000011349127],"about_ca_topic_score_codex":0.0065076686,"about_ca_topic_score_gemma":0.0068857404,"teacher_disagreement_score":0.0065076686,"about_ca_system_score_codex":0.0003787574,"about_ca_system_score_gemma":0.0004795015,"threshold_uncertainty_score":0.012939572},"labels":[],"label_agreement":null},{"id":"W2946589254","doi":"10.1016/j.evolhumbehav.2019.05.003","title":"Response to vocal music in Angelman syndrome contrasts with Prader-Willi syndrome","year":2019,"lang":"en","type":"article","venue":"Evolution and Human Behavior","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":19,"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":"Natural Sciences and Engineering Research Council of Canada; National Institutes of Health; Harvard University","keywords":"Angelman syndrome; Offspring; Genomic imprinting; Imprinting (psychology); Psychology; Parent–offspring conflict; Developmental psychology; Parental investment; Biology; Genetics; Gene; Pregnancy","score_opus":0.010116746861948031,"score_gpt":0.24203751178537003,"score_spread":0.231920764923422,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2946589254","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9974107,0.00012626125,0.00026262208,0.00010207849,0.00001908947,0.0000043874843,0.00005627201,0.00002216492,0.0019963311],"genre_scores_gemma":[0.99927825,0.000060365615,0.00020539257,0.00003021551,0.000020881067,0.0000034319091,0.000032326825,0.000013864416,0.000355184],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9997596,0.000055628752,0.000032458986,0.00004668013,0.00006664847,0.000039075305],"domain_scores_gemma":[0.9992262,0.00035172052,0.00023262676,0.00004124371,0.00004323879,0.000104929015],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00018341992,0.00045755273,0.0003179968,0.0009921144,0.00020313913,0.00028383653,0.00031936765,0.000658533,0.003791681],"category_scores_gemma":[0.0021073401,0.00016274572,0.00021038961,0.00029907268,0.0007344882,0.00020178303,0.00040071973,0.00031210927,0.00038975244],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0010746811,0.000096575015,0.21371934,0.00011423148,0.00010202573,0.16509637,0.0021418352,0.00041747018,0.60213166,0.0017141569,0.0003565627,0.0130351735],"study_design_scores_gemma":[0.000061882194,0.00040033768,0.70950264,0.000022019645,0.00012062439,0.25578612,0.0010432488,0.0008514944,0.02994506,0.0007400176,0.0014899763,0.00003659269],"about_ca_topic_score_codex":0.0011515586,"about_ca_topic_score_gemma":0.0013419905,"teacher_disagreement_score":0.003791681,"about_ca_system_score_codex":0.00014615244,"about_ca_system_score_gemma":0.00018356215,"threshold_uncertainty_score":0.012684464},"labels":[],"label_agreement":null},{"id":"W2949563565","doi":"","title":"305 CHYLOTHORAX IN AN INFANT WITH FEATURES OF PETERS PLUS SYNDROME.","year":2007,"lang":"en","type":"article","venue":"Journal of Investigative Medicine","topic":"Genetic Syndromes and Imprinting","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":"University of British Columbia","funders":"","keywords":"Medicine; Polyhydramnios; Ductus arteriosus; Etiology; Chylothorax; Cardiology; Internal medicine; Pathology; Gestation; Pregnancy","score_opus":0.019585386787861404,"score_gpt":0.2785593719628053,"score_spread":0.25897398517494385,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2949563565","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99449265,0.0009243837,0.001026387,0.0004664323,0.00010473265,0.000074033924,0.00016210871,0.00010163261,0.002647704],"genre_scores_gemma":[0.99869883,0.00032836787,0.00035080983,0.00009515274,0.00010061476,0.000009835673,0.00007773372,0.000008540827,0.0003300428],"study_design_codex":"case_report","study_design_gemma":"case_report","domain_scores_codex":[0.99958664,0.000058406535,0.000041359403,0.00007131103,0.00009701971,0.00014525309],"domain_scores_gemma":[0.9991437,0.00025627372,0.00020068516,0.00003948214,0.000043565757,0.00031627354],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00029210214,0.0010767991,0.0007013859,0.0014954681,0.0009840145,0.00068271824,0.0004333778,0.0022193664,0.0014251276],"category_scores_gemma":[0.0026390033,0.0007143013,0.00056798826,0.0005169045,0.00083705445,0.0006583557,0.0009860172,0.0013723935,0.000305489],"study_design_candidate":"case_report","study_design_consensus":"case_report","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.000037800986,0.000021260215,0.013297397,0.000026116168,0.000007281693,0.9833589,0.00010059922,0.000041522435,0.0017709499,0.00011299839,0.00015545772,0.001069764],"study_design_scores_gemma":[0.000009289928,0.00019608132,0.018420313,0.00001099229,0.000014340849,0.9801521,0.0000733698,0.0002280665,0.00053829444,0.00006553855,0.00028259147,0.000008961556],"about_ca_topic_score_codex":0.0017723215,"about_ca_topic_score_gemma":0.002097166,"teacher_disagreement_score":0.0022193664,"about_ca_system_score_codex":0.00054896146,"about_ca_system_score_gemma":0.0005047623,"threshold_uncertainty_score":0.0047674775},"labels":[],"label_agreement":null},{"id":"W2956085547","doi":"10.7554/elife.45282","title":"Fetal and trophoblast PI3K p110α have distinct roles in regulating resource supply to the growing fetus in mice","year":2019,"lang":"en","type":"article","venue":"eLife","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":45,"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 Calgary","funders":"Erasmus+; Biotechnology and Biological Sciences Research Council; Royal Society; Medical Research Council; European Cooperation in Science and Technology; Wellcome Trust","keywords":"Trophoblast; Conceptus; Biology; Placenta; Fetus; Cell biology; Phenotype; Embryonic stem cell; Genetics; Gene; Pregnancy","score_opus":0.0045721865324490595,"score_gpt":0.21024307467844808,"score_spread":0.20567088814599901,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2956085547","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.93201745,0.0045874906,0.03928397,0.00134238,0.00035454013,0.00011082153,0.00987742,0.0019999773,0.010426026],"genre_scores_gemma":[0.94396347,0.0040184376,0.018476639,0.0005389629,0.000043517928,0.00032499578,0.0046969703,0.0010729542,0.026863933],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9994073,0.0000436393,0.00006501635,0.00019811014,0.00018661378,0.000099352],"domain_scores_gemma":[0.9995004,0.000067801084,0.00018498834,0.000048734888,0.000019496827,0.00017849191],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00039537987,0.00077804783,0.00046025586,0.001514469,0.00048179063,0.0011580957,0.00068728306,0.0010799684,0.004289536],"category_scores_gemma":[0.00033735507,0.0010114425,0.0008145265,0.0005091417,0.001219752,0.00066544034,0.000916185,0.0036877529,0.001385726],"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":[0.00078847114,0.00004217493,0.0009251148,0.00012914959,0.000034873035,0.00045394417,0.00009244811,0.000271589,0.98931456,0.001730732,0.00032285936,0.005893921],"study_design_scores_gemma":[0.00018868632,0.00026174428,0.014532975,0.000065826,0.00015898909,0.0023591158,0.00019294125,0.0020130225,0.9562661,0.0011822613,0.022741897,0.00003646688],"about_ca_topic_score_codex":0.0013203853,"about_ca_topic_score_gemma":0.002088999,"teacher_disagreement_score":0.004289536,"about_ca_system_score_codex":0.00085594837,"about_ca_system_score_gemma":0.0006060621,"threshold_uncertainty_score":0.014349937},"labels":[],"label_agreement":null},{"id":"W2961087513","doi":"10.1097/mph.0000000000001555","title":"Challenges in the Diagnosis of Medulloblastoma Recurrence at an Unusual Site in a Patient With Prader-Willi Syndrome","year":2019,"lang":"en","type":"article","venue":"Journal of Pediatric Hematology/Oncology","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","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":"Hospital for Sick Children","funders":"Brain Tumour Charity","keywords":"Medulloblastoma; Medicine; Pediatrics; Histology; Biopsy; Pathology","score_opus":0.024332796119822298,"score_gpt":0.2818840949584432,"score_spread":0.2575512988386209,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2961087513","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.94796324,0.011164485,0.009482148,0.020899912,0.0007064796,0.00014489546,0.00026064273,0.000365749,0.009012419],"genre_scores_gemma":[0.98721886,0.003534405,0.0060871323,0.0015058263,0.0009871015,0.000027237491,0.00009866445,0.000045029767,0.0004956672],"study_design_codex":"case_report","study_design_gemma":"case_report","domain_scores_codex":[0.999228,0.00015789023,0.00013412499,0.00012532096,0.00016983566,0.0001848108],"domain_scores_gemma":[0.99800855,0.0007783301,0.0003567042,0.00012744578,0.0003130241,0.0004160272],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0010435241,0.0005640456,0.00079136225,0.0014048022,0.0012356867,0.001350998,0.0012188978,0.0023387768,0.0011633642],"category_scores_gemma":[0.0053671715,0.00050646934,0.00056612573,0.000539885,0.0009933686,0.0018351645,0.0007774378,0.0026184928,0.0010351662],"study_design_candidate":"case_report","study_design_consensus":"case_report","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.000104303166,0.000041410112,0.1133991,0.000106641906,0.000019537,0.8612193,0.0007468781,0.00036055167,0.0032899356,0.0004593199,0.0026333043,0.017619807],"study_design_scores_gemma":[0.000006961264,0.00006314751,0.0126578035,0.000076171964,0.000026187461,0.9809429,0.0012647439,0.00096217915,0.0010109218,0.000732866,0.0022412231,0.000014960321],"about_ca_topic_score_codex":0.002638096,"about_ca_topic_score_gemma":0.0038064518,"teacher_disagreement_score":0.002638096,"about_ca_system_score_codex":0.00085287873,"about_ca_system_score_gemma":0.00080184254,"threshold_uncertainty_score":0.006188154},"labels":[],"label_agreement":null},{"id":"W2964455242","doi":"10.1101/723254","title":"Evolution of imprinting via lineage-specific insertion of retroviral promoters","year":2019,"lang":"en","type":"preprint","venue":"bioRxiv (Cold Spring Harbor Laboratory)","topic":"Genetic Syndromes and Imprinting","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 British Columbia","funders":"","keywords":"Biology; Genomic imprinting; Genetics; Endogenous retrovirus; Germline; Gene; Epigenetics; DNA methylation; Allele; Imprinting (psychology); CRISPR; Transcription (linguistics); Genome; Gene expression","score_opus":0.00872867119547473,"score_gpt":0.20293498455257641,"score_spread":0.19420631335710167,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2964455242","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.93163717,0.0015627918,0.05760644,0.00022676171,0.00006714567,0.00008001214,0.00049397274,0.0006495144,0.007676248],"genre_scores_gemma":[0.98072225,0.00090929394,0.012852938,0.000068112065,0.000016472623,0.0000386971,0.0005190253,0.00011052622,0.0047626565],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99979967,0.000034019187,0.000018921137,0.000057918776,0.00005527681,0.000034167286],"domain_scores_gemma":[0.99979275,0.000047463676,0.000080518905,0.00004086185,0.000013126787,0.000025283562],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00032619125,0.0002839903,0.000112124886,0.0003611212,0.00017589494,0.0004329213,0.000546196,0.00024547245,0.001036299],"category_scores_gemma":[0.00022572669,0.0002229327,0.00020192699,0.00014652709,0.00033169988,0.0002494943,0.0006229803,0.00081437716,0.00049406604],"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":[0.000037372734,0.000012074315,0.001243511,0.000026140382,0.0000071286245,0.00014077312,0.00006246406,0.00018040373,0.99001896,0.0024639757,0.000049155948,0.0057581123],"study_design_scores_gemma":[0.000017649658,0.000121247256,0.006346995,0.00002314232,0.000033064218,0.0012123599,0.000059736103,0.0045292387,0.9697082,0.0008554628,0.017080842,0.00001207456],"about_ca_topic_score_codex":0.0003435701,"about_ca_topic_score_gemma":0.0005337246,"teacher_disagreement_score":0.001036299,"about_ca_system_score_codex":0.00042812107,"about_ca_system_score_gemma":0.00023724634,"threshold_uncertainty_score":0.0034667253},"labels":[],"label_agreement":null},{"id":"W2965756418","doi":"10.1101/717868","title":"Imprinted maternally-expressed microRNAs antagonize paternally-driven gene programs in neurons","year":2019,"lang":"en","type":"preprint","venue":"bioRxiv (Cold Spring Harbor Laboratory)","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":3,"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 Cancer Institute; Fonds de Recherche du Québec - Santé; Natural Sciences and Engineering Research Council of Canada; National Institutes of Health; Koch Institute for Integrative Cancer Research, Massachusetts Institute of Technology","keywords":"Genomic imprinting; Biology; microRNA; Gene; Gene cluster; Genetics; Psychological repression; Regulation of gene expression; Gene expression; DNA methylation","score_opus":0.013708305574120259,"score_gpt":0.21355734898681256,"score_spread":0.1998490434126923,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2965756418","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.98620474,0.0005746131,0.00807427,0.0000908069,0.00004430465,0.0000062588856,0.00021465018,0.000138389,0.004652032],"genre_scores_gemma":[0.9928445,0.00024438286,0.002468275,0.000039963023,0.00000820011,0.0000067790384,0.00015704773,0.00005070048,0.004180093],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9998919,0.000016060436,0.0000072763405,0.000025742505,0.000038008326,0.000020970823],"domain_scores_gemma":[0.99991,0.000021460864,0.000024210722,0.000014915551,0.0000088832985,0.000020482983],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00009747641,0.00020040174,0.00015217415,0.00013383616,0.00010521284,0.00028764308,0.00014135284,0.00014949148,0.0014623293],"category_scores_gemma":[0.00014967176,0.00012055005,0.00012720498,0.00006483485,0.00019621705,0.0001182799,0.00026439762,0.0002966809,0.0004564908],"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":[0.000042641215,0.0000044170033,0.0009116946,0.000014463004,0.000004797603,0.00011606071,0.000013831659,0.00012850465,0.99643636,0.0006754365,0.000062497726,0.0015893284],"study_design_scores_gemma":[0.000005513618,0.00002919122,0.00692454,0.000003755302,0.000009802969,0.00042335805,0.00002931872,0.0015719185,0.9878109,0.00041697538,0.002772206,0.000002477659],"about_ca_topic_score_codex":0.00032559442,"about_ca_topic_score_gemma":0.0007143499,"teacher_disagreement_score":0.0014623293,"about_ca_system_score_codex":0.00028959956,"about_ca_system_score_gemma":0.00021301933,"threshold_uncertainty_score":0.0048919916},"labels":[],"label_agreement":null},{"id":"W2968123855","doi":"10.1186/s13072-019-0295-4","title":"ZFP57 regulation of transposable elements and gene expression within and beyond imprinted domains","year":2019,"lang":"en","type":"article","venue":"Epigenetics & Chromatin","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":67,"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":"Biotechnology and Biological Sciences Research Council; Medical Research Council; Wellcome Trust; Wellcome","keywords":"Biology; DNA methylation; Genomic imprinting; Genetics; Transposable element; Chromatin; Differentially methylated regions; Epigenetics; RNA-Directed DNA Methylation; Epigenomics; Regulation of gene expression; Epigenetics of physical exercise; Gene; Genome; Gene expression","score_opus":0.004894203272541832,"score_gpt":0.21827363984481293,"score_spread":0.2133794365722711,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2968123855","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.98000216,0.0045149745,0.009360858,0.00011730318,0.00003523404,0.000015517717,0.0011322233,0.00023554199,0.0045860554],"genre_scores_gemma":[0.9922191,0.0010189821,0.0021496878,0.00004624961,0.000011542384,0.000013696701,0.00079554395,0.000043207663,0.0037020247],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9999074,0.000003982949,0.000005105553,0.000035455854,0.000023748746,0.000024285951],"domain_scores_gemma":[0.99989855,0.000017308448,0.000040481267,0.000009317887,0.000011907965,0.00002241166],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00009533615,0.0002794762,0.0001419684,0.00019194125,0.00014394493,0.00032449063,0.00031376927,0.00021649452,0.002336627],"category_scores_gemma":[0.00017323348,0.00011173968,0.00018480748,0.00015865618,0.00028678408,0.0002552504,0.0004319894,0.0003528728,0.0007030938],"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":[0.000111845744,0.0000085942465,0.0028663054,0.00008616162,0.000008887427,0.0001752779,0.000033333527,0.00022156168,0.98838335,0.0008967752,0.00016057675,0.00704743],"study_design_scores_gemma":[0.00002928793,0.00010728682,0.06580367,0.000031851287,0.000030378365,0.0008421878,0.0000553669,0.0034134479,0.9203531,0.00081787934,0.008505565,0.00000993692],"about_ca_topic_score_codex":0.00062646606,"about_ca_topic_score_gemma":0.00057941175,"teacher_disagreement_score":0.002336627,"about_ca_system_score_codex":0.00039836057,"about_ca_system_score_gemma":0.00017434357,"threshold_uncertainty_score":0.007816792},"labels":[],"label_agreement":null},{"id":"W2969359780","doi":"10.1093/biolre/ioz168","title":"Resiliency of equid H19 imprint to somatic cell reprogramming by oocyte nuclear transfer and genetically induced pluripotency†","year":2019,"lang":"en","type":"article","venue":"Biology of Reproduction","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":5,"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","funders":"Natural Sciences and Engineering Research Council of Canada","keywords":"Reprogramming; Somatic cell nuclear transfer; Biology; Genomic imprinting; Imprinting (psychology); Epigenetics; Induced pluripotent stem cell; DNA methylation; Somatic cell; Genetics; Embryonic stem cell; Differentially methylated regions; Cell biology; Methylation; Embryo; Gene; Gene expression; Blastocyst; Embryogenesis","score_opus":0.0069012412677957975,"score_gpt":0.22639805056229148,"score_spread":0.2194968092944957,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2969359780","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9911431,0.0010594026,0.00477278,0.00005180576,0.000015513859,0.00003805816,0.000318627,0.000046349942,0.002554478],"genre_scores_gemma":[0.99456245,0.00045979102,0.0014059303,0.000033555545,0.0000046169225,0.0000355801,0.00055869884,0.000023014733,0.00291642],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9998486,0.000018327022,0.000015218201,0.00004976146,0.000043569766,0.000024419478],"domain_scores_gemma":[0.9998996,0.000024681927,0.000029452833,0.000018031735,0.00001269129,0.000015526264],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00019301432,0.0001703129,0.00014488435,0.0002534839,0.0001786155,0.00023818988,0.00020508724,0.00023232216,0.002020998],"category_scores_gemma":[0.00020061032,0.00008138713,0.00012377344,0.00010324704,0.0002786017,0.00021536073,0.00027774458,0.0002541215,0.00024339685],"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":[0.000037265025,0.000007592424,0.0009895959,0.000019658743,0.000004682243,0.00009915585,0.000044529927,0.000050699375,0.9962335,0.00013901404,0.000013937118,0.002360389],"study_design_scores_gemma":[0.000005389502,0.00023584861,0.040931135,0.000007780647,0.000020173557,0.0010429262,0.00013208968,0.0006743805,0.95133203,0.00015356814,0.005456911,0.000007730309],"about_ca_topic_score_codex":0.0004928126,"about_ca_topic_score_gemma":0.0007835948,"teacher_disagreement_score":0.002020998,"about_ca_system_score_codex":0.00020085511,"about_ca_system_score_gemma":0.00013824803,"threshold_uncertainty_score":0.0067608953},"labels":[],"label_agreement":null},{"id":"W2972063248","doi":"10.1016/j.stem.2019.06.013","title":"Distinct Imprinting Signatures and Biased Differentiation of Human Androgenetic and Parthenogenetic Embryonic Stem Cells","year":2019,"lang":"en","type":"article","venue":"Cell stem cell","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":40,"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; United States-Israel Binational Science Foundation; New York State Stem Cell Science","keywords":"Genomic imprinting; Biology; Imprinting (psychology); Epigenetics; Embryonic stem cell; Induced pluripotent stem cell; Genetics; Reprogramming; X-inactivation; DNA methylation; Gene; Gene expression; X chromosome","score_opus":0.007473356786152542,"score_gpt":0.2000458829801031,"score_spread":0.19257252619395054,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2972063248","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9969798,0.0006604604,0.00082212867,0.000028685366,0.000007006053,0.0000051945926,0.00029779843,0.000031845328,0.0011670599],"genre_scores_gemma":[0.9974064,0.00037147372,0.00042686798,0.000024691632,0.000004361242,0.0000067520355,0.00048800925,0.000017828834,0.0012534627],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99988186,0.000016772492,0.00000996401,0.000020349835,0.000046292804,0.000024779412],"domain_scores_gemma":[0.9998486,0.0000410611,0.000036949932,0.000022082273,0.000021869324,0.000029462397],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00010448697,0.00013146784,0.00019439934,0.0005789991,0.00010730464,0.00035245813,0.0001248812,0.00013232545,0.00096330506],"category_scores_gemma":[0.00022874035,0.00014525908,0.00012843404,0.000306117,0.00019908154,0.00010543098,0.00023316608,0.00019472121,0.00022687177],"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":[0.00012414757,0.0000036758324,0.002171737,0.000010801739,0.000006556374,0.00009735482,0.00004749426,0.00004032866,0.995413,0.0002388853,0.000017599226,0.0018285593],"study_design_scores_gemma":[0.000018572771,0.00014934113,0.18035232,0.000006025626,0.00005154367,0.0019694034,0.0001709576,0.00056471804,0.81354666,0.0003519926,0.0028069578,0.000011517402],"about_ca_topic_score_codex":0.0006700069,"about_ca_topic_score_gemma":0.0010949398,"teacher_disagreement_score":0.00096330506,"about_ca_system_score_codex":0.0001527079,"about_ca_system_score_gemma":0.0001786574,"threshold_uncertainty_score":0.0032225847},"labels":[],"label_agreement":null},{"id":"W2978823510","doi":"10.1038/s41436-019-0657-0","title":"Widening of the genetic and clinical spectrum of Lamb–Shaffer syndrome, a neurodevelopmental disorder due to SOX5 haploinsufficiency","year":2019,"lang":"en","type":"article","venue":"Genetics in Medicine","topic":"Genetic Syndromes and Imprinting","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":"Hospital for Sick Children; McGill University; SickKids Foundation; Dalhousie University; University of Toronto; Montreal Children's Hospital; Izaak Walton Killam Health Centre","funders":"National Institute of Arthritis and Musculoskeletal and Skin Diseases; Center for Individualized Medicine, Mayo Clinic; Institut National de la Santé et de la Recherche Médicale; Assistance Publique - Hôpitaux de Paris; National Institute for Health and Care Research; Cleveland Clinic; Wellcome Trust; Assistance publique-Hôpitaux de Paris; Agence Nationale de la Recherche","keywords":"Haploinsufficiency; Missense mutation; Genetics; Transactivation; Biology; Phenotype; Transcription factor; Bioinformatics; Gene","score_opus":0.010466189557652297,"score_gpt":0.27111945980091945,"score_spread":0.2606532702432672,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2978823510","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.98323405,0.002506755,0.0029000298,0.0008878818,0.000068663314,0.000026927788,0.0004729029,0.0001095923,0.009793026],"genre_scores_gemma":[0.9971488,0.00064521446,0.0011076523,0.0001568919,0.00004190806,0.000007584456,0.00013568865,0.000023237846,0.00073296926],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9995931,0.00005959502,0.000055028253,0.000107163774,0.00012989243,0.000055214714],"domain_scores_gemma":[0.99931955,0.00030460503,0.00010555218,0.000038004546,0.00008784958,0.0001444831],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00040132413,0.0010991032,0.00046775723,0.002060696,0.00035571505,0.00033003913,0.00037954122,0.00066829234,0.0036718042],"category_scores_gemma":[0.0013911149,0.00018591901,0.00034448894,0.0005893795,0.0011434244,0.00038550128,0.0008142565,0.00042504724,0.00030542928],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0015406962,0.00016340456,0.11585183,0.00037309714,0.0002551052,0.3719065,0.001315476,0.0016463662,0.42833874,0.006141575,0.0024537956,0.07001341],"study_design_scores_gemma":[0.00011026076,0.0003218503,0.33617005,0.00022841306,0.00031291548,0.6057889,0.00077267684,0.0018643643,0.039873444,0.004547866,0.009935252,0.00007404371],"about_ca_topic_score_codex":0.0012391136,"about_ca_topic_score_gemma":0.0014721958,"teacher_disagreement_score":0.0036718042,"about_ca_system_score_codex":0.00018864538,"about_ca_system_score_gemma":0.00037829045,"threshold_uncertainty_score":0},"labels":[],"label_agreement":null},{"id":"W2982377894","doi":"10.1186/s13059-019-1833-x","title":"Endogenous retroviral insertions drive non-canonical imprinting in extra-embryonic tissues","year":2019,"lang":"en","type":"article","venue":"Genome biology","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":96,"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 Calgary","funders":"European Research Council; Medical Research Council; Fondazione Pierfranco e Luisa Mariani; Bundesministerium für Bildung und Forschung; E-Rare; Agence Nationale de la Recherche; Biotechnology and Biological Sciences Research Council; Ministero della Salute","keywords":"Biology; Endogenous retrovirus; Imprinting (psychology); Embryonic stem cell; Genomic imprinting; Genetics; Computational biology; Human genetics; Endogeny; Evolutionary biology; Cell biology; Genome; Gene; DNA methylation; Gene expression","score_opus":0.014500278220783753,"score_gpt":0.24514050205476504,"score_spread":0.23064022383398128,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2982377894","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.96754104,0.0021651415,0.019292602,0.00019370028,0.0001811038,0.00029453068,0.002332247,0.0008420145,0.007157663],"genre_scores_gemma":[0.95557505,0.0011478036,0.014545668,0.00015327863,0.000041334053,0.00018936647,0.005516455,0.00029468603,0.022536423],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99953675,0.000041264397,0.00005160382,0.00011378644,0.00015757928,0.000099111894],"domain_scores_gemma":[0.9996101,0.00008402626,0.00013013062,0.000068301655,0.000022943148,0.00008444253],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0003093209,0.0006719672,0.00019047124,0.0004009832,0.00020572868,0.0004795774,0.0009109157,0.0005448732,0.004794605],"category_scores_gemma":[0.00018345927,0.000411299,0.00037157015,0.00027607734,0.00042750203,0.00026143747,0.0005709939,0.0014234268,0.0014874757],"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":[0.000041658743,0.00003017981,0.00018567611,0.00003644291,0.0000048242537,0.000068393965,0.00002104097,0.000029286528,0.9982956,0.00036254735,0.000039878934,0.00088446477],"study_design_scores_gemma":[0.000062485116,0.00028433083,0.005223556,0.000021115278,0.000040650993,0.0006614415,0.00004378364,0.0010564494,0.9824563,0.00014928768,0.009993219,0.000007344736],"about_ca_topic_score_codex":0.00040057462,"about_ca_topic_score_gemma":0.0011191246,"teacher_disagreement_score":0.004794605,"about_ca_system_score_codex":0.00052916846,"about_ca_system_score_gemma":0.00030447595,"threshold_uncertainty_score":0.01603955},"labels":[],"label_agreement":null},{"id":"W2983259024","doi":"10.1002/ajmg.c.31754","title":"PRC2‐complex related dysfunction in overgrowth syndromes: A review of <i>EZH2</i>, <i>EED</i>, and <i>SUZ12</i> and their syndromic phenotypes","year":2019,"lang":"en","type":"review","venue":"American Journal of Medical Genetics Part C Seminars in Medical Genetics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":77,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"BC Children's Hospital; University of British Columbia","funders":"Canadian Institutes of Health Research; BC Children's Hospital","keywords":"Phenotype; Medicine; EZH2; PRC2; Genetics; Biology; Epigenetics","score_opus":0.021459204881092188,"score_gpt":0.308190557840712,"score_spread":0.28673135295961977,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2983259024","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":[0.00080278685,0.9973648,0.00034437721,0.00041060883,0.00029126272,0.0000074695986,0.000047889233,0.000015563794,0.00071526406],"genre_scores_gemma":[0.0023463666,0.9955668,0.00056274864,0.00039991335,0.0005311787,0.0000119751385,0.000112927424,0.0000036653691,0.00046438168],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.999759,0.000035080848,0.000080878664,0.000045836594,0.000057565816,0.00002158504],"domain_scores_gemma":[0.9996449,0.00015843585,0.00007987538,0.00000685729,0.0000649129,0.00004507316],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00039505455,0.00080613006,0.0009305058,0.0035618069,0.00024917218,0.00064230064,0.00065281184,0.00076176925,0.0017520622],"category_scores_gemma":[0.00071620307,0.00027027473,0.00057901983,0.0029546435,0.0003981863,0.0009790587,0.000573817,0.0009325373,0.0006462187],"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":[0.00012948235,0.00008486591,0.003067903,0.027441775,0.0003997209,0.004852663,0.00037576992,0.00053806795,0.005810893,0.002480815,0.06739202,0.88742596],"study_design_scores_gemma":[0.00002879407,0.00019400488,0.010311426,0.005744615,0.0005704584,0.042237382,0.00027019062,0.00024356207,0.0010616959,0.0011784498,0.9381026,0.00005690519],"about_ca_topic_score_codex":0.0011756355,"about_ca_topic_score_gemma":0.0017100476,"teacher_disagreement_score":0.0035618069,"about_ca_system_score_codex":0.00039843068,"about_ca_system_score_gemma":0.0008700839,"threshold_uncertainty_score":0.005861163},"labels":[],"label_agreement":null},{"id":"W2987490438","doi":"10.1111/gtc.12736","title":"Characterization of genetic‐origin‐dependent monoallelic expression in mouse embryonic stem cells","year":2019,"lang":"en","type":"article","venue":"Genes to Cells","topic":"Genetic Syndromes and Imprinting","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 British Columbia","funders":"Japan Society for the Promotion of Science; Takeda Medical Research Foundation","keywords":"Biology; Epigenetics; Embryonic stem cell; Genetics; Genomic imprinting; Retrotransposon; Gene; Allele; Induced pluripotent stem cell; X-inactivation; DNA methylation; Gene expression; X chromosome; Transposable element; Genome","score_opus":0.008496817429384778,"score_gpt":0.216265221183739,"score_spread":0.20776840375435424,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2987490438","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9900594,0.0012880723,0.006745513,0.000017712835,0.0000044415524,0.000037804573,0.0008461317,0.000059385904,0.0009414962],"genre_scores_gemma":[0.991601,0.00068130635,0.0038099755,0.00004136817,0.0000050368635,0.000064370426,0.0019089351,0.00003588211,0.0018520958],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9998424,0.0000143511925,0.000022988848,0.000039869257,0.000054470078,0.000025863157],"domain_scores_gemma":[0.9997868,0.000038557966,0.0000620488,0.000039850922,0.000031474356,0.000041305986],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0001617374,0.00016307675,0.00017318543,0.00057669333,0.00011431822,0.00026170854,0.00019088777,0.00019655412,0.0006690951],"category_scores_gemma":[0.00015270557,0.00017286967,0.00018762989,0.00028498788,0.00012733096,0.00012633849,0.0002773471,0.00028363583,0.00037777508],"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":[0.000019048615,0.0000038387166,0.0013838604,0.000012793246,0.0000028959632,0.000034573237,0.000014092408,0.00001653278,0.9976708,0.000034261455,0.0000039356755,0.00080340164],"study_design_scores_gemma":[0.0000059133936,0.00019151969,0.10858384,0.000010077908,0.00003692549,0.00097116217,0.00006545583,0.0008575528,0.88662654,0.00008646467,0.002555562,0.0000089381165],"about_ca_topic_score_codex":0.00040791382,"about_ca_topic_score_gemma":0.0009139595,"teacher_disagreement_score":0.0006690951,"about_ca_system_score_codex":0.00011769172,"about_ca_system_score_gemma":0.000120767734,"threshold_uncertainty_score":0.0022383332},"labels":[],"label_agreement":null},{"id":"W2989504433","doi":"10.1139/cjas-2018-0253","title":"Analysis of porcine <i>OSBPL5</i> gene allelic expression in skeletal muscle and association of a single-nucleotide polymorphism in the coding region with production traits","year":2019,"lang":"en","type":"article","venue":"Canadian Journal of Animal Science","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":0,"is_retracted":false,"has_abstract":true,"route_ca_aff":false,"route_ca_fund":false,"route_ca_venue":true,"route_about_ca":false,"ca_institutions":"","funders":"","keywords":"Biology; Single-nucleotide polymorphism; Genotype; Allele; SNP; Genetics; Imprinting (psychology); Gene; Genomic imprinting; Coding region; Gene expression; Molecular biology; DNA methylation","score_opus":0.010079440442688062,"score_gpt":0.2072850765852229,"score_spread":0.19720563614253483,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2989504433","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9988593,0.00008431933,0.0006782322,0.000014219488,0.0000024868962,0.000003016454,0.00013075884,0.0000038968715,0.00022371217],"genre_scores_gemma":[0.99890983,0.000040296753,0.0005017478,0.000027567354,0.0000026771982,0.0000068446975,0.00021212542,0.0000041489775,0.00029482535],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9998815,0.00002225881,0.000009872644,0.000044132965,0.000024029485,0.000018147924],"domain_scores_gemma":[0.9998609,0.000033377368,0.00006616009,0.0000077181085,0.000009795771,0.000022123944],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00017715362,0.00014928564,0.00012346661,0.00036509437,0.00011441397,0.00012929135,0.00012925165,0.00017194593,0.0009913585],"category_scores_gemma":[0.00018733385,0.00007125208,0.00022782401,0.00029790137,0.00015416068,0.000048840175,0.0001071946,0.00016408577,0.00011985614],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0008108227,0.000044927143,0.31993577,0.000068662164,0.00014895736,0.0009413901,0.00016932703,0.00012979734,0.6675689,0.00012561688,0.00010279836,0.009953047],"study_design_scores_gemma":[0.000012078033,0.00012921478,0.9873891,0.0000067510605,0.00005000647,0.00087117444,0.00006143104,0.0005383616,0.01042362,0.000035468016,0.0004777486,0.0000050162635],"about_ca_topic_score_codex":0.0018480583,"about_ca_topic_score_gemma":0.0028925173,"teacher_disagreement_score":0.0018480583,"about_ca_system_score_codex":0.00010370884,"about_ca_system_score_gemma":0.00008597819,"threshold_uncertainty_score":0.0036745667},"labels":[],"label_agreement":null},{"id":"W2990673862","doi":"10.6000/2292-2598.2019.07.04.4","title":"Outstretched Index Finger - A Pointer is Peculiar Behaviour Characteristic of Angelman Syndrome in Adults – A Case Series Study","year":2019,"lang":"en","type":"article","venue":"Journal of Intellectual Disability - Diagnosis and Treatment","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":0,"is_retracted":false,"has_abstract":true,"route_ca_aff":false,"route_ca_fund":false,"route_ca_venue":true,"route_about_ca":false,"ca_institutions":"","funders":"","keywords":"Angelman syndrome; Pointer (user interface); Index (typography); Psychology; Series (stratigraphy); Index finger; Audiology; Computer science; Medicine; Artificial intelligence; Geology; Anatomy; World Wide Web","score_opus":0.013684549450089727,"score_gpt":0.2602945599648094,"score_spread":0.24661001051471965,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2990673862","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9963858,0.0013780026,0.000599023,0.00008484812,0.000026434669,0.000036636175,0.00007846187,0.000027610347,0.0013830713],"genre_scores_gemma":[0.99837047,0.00066325127,0.0002760219,0.0000616538,0.00008038642,0.000009289762,0.0000637287,0.0000065529284,0.00046864105],"study_design_codex":"case_report","study_design_gemma":"case_report","domain_scores_codex":[0.99960274,0.000042237847,0.00006739838,0.00013598274,0.00006454756,0.00008706723],"domain_scores_gemma":[0.9989661,0.0002303186,0.00035190285,0.000100229445,0.00006647031,0.00028499335],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00022398775,0.000984473,0.0005841202,0.0011654278,0.0006906823,0.0006350045,0.00034476083,0.0011530443,0.0021474978],"category_scores_gemma":[0.001353189,0.00046670772,0.00037508426,0.00072391145,0.0009094255,0.0006547749,0.00060251006,0.0005570225,0.00063503993],"study_design_candidate":"case_report","study_design_consensus":"case_report","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.000106262196,0.00007172261,0.12774813,0.00006009422,0.00003017868,0.86355317,0.0006793187,0.000062833446,0.0026945479,0.00011624001,0.00036818214,0.0045093438],"study_design_scores_gemma":[0.000007645036,0.00013162602,0.037053112,0.00001124809,0.000021405627,0.96148074,0.00028320024,0.00007478911,0.00038286293,0.000037482838,0.0005051403,0.000010848629],"about_ca_topic_score_codex":0.0012954497,"about_ca_topic_score_gemma":0.0015466543,"teacher_disagreement_score":0.0021474978,"about_ca_system_score_codex":0.00028257855,"about_ca_system_score_gemma":0.00036412498,"threshold_uncertainty_score":0.007184088},"labels":[],"label_agreement":null},{"id":"W2991788166","doi":"","title":"Characterizing the phenotypic spectrum of Peters anomaly: from mild to severe disease","year":2015,"lang":"en","type":"article","venue":"Investigative Ophthalmology & Visual Science","topic":"Genetic Syndromes and Imprinting","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":"Hospital for Sick Children","funders":"","keywords":"Anomaly (physics); Spectrum (functional analysis); Phenotype; Disease; Clinical phenotype; Medicine; Genetics; Biology; Internal medicine; Physics; Gene","score_opus":0.038259411159624904,"score_gpt":0.303362438156321,"score_spread":0.26510302699669613,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2991788166","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99156874,0.00049081683,0.003362713,0.00029492026,0.0000119142815,0.000027571861,0.00030066652,0.00011034794,0.003832299],"genre_scores_gemma":[0.99789196,0.00030612783,0.0014259869,0.000047126996,0.000019509906,0.000006144758,0.000106142084,0.000022794127,0.00017410298],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9995314,0.000074186115,0.00006702757,0.00010406978,0.0001346139,0.000088684974],"domain_scores_gemma":[0.99905366,0.0003133755,0.0002328116,0.00005140509,0.00013350109,0.00021522028],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0004551443,0.00070053653,0.00040769123,0.0026267536,0.0003030361,0.0005409025,0.0003589145,0.00035479217,0.0014509824],"category_scores_gemma":[0.002718448,0.00013607902,0.00020789063,0.0006643004,0.0008488893,0.0005061921,0.0009709006,0.0005122813,0.00020919742],"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":[0.0010022909,0.00017398444,0.6720332,0.00024182153,0.00014611748,0.03523752,0.001386681,0.0014225169,0.20486033,0.002839381,0.0020490624,0.0786071],"study_design_scores_gemma":[0.000038740476,0.0004643257,0.8444231,0.00008680298,0.00016072878,0.1161946,0.0012086979,0.002150553,0.02802613,0.0048382115,0.0023598885,0.000048264228],"about_ca_topic_score_codex":0.00087373814,"about_ca_topic_score_gemma":0.0011076581,"teacher_disagreement_score":0.0026267536,"about_ca_system_score_codex":0.00018203739,"about_ca_system_score_gemma":0.00029720066,"threshold_uncertainty_score":0.0048540235},"labels":[],"label_agreement":null},{"id":"W2996944597","doi":"10.1111/obr.12992","title":"Current and emerging therapies for managing hyperphagia and obesity in Prader‐Willi syndrome: A narrative review","year":2019,"lang":"en","type":"review","venue":"Obesity Reviews","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":89,"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":"Millendo Therapeutics","keywords":"Medicine; Appetite; Weight gain; Weight loss; Obesity; Narrative review; Clinical trial; Intensive care medicine; Pediatrics; Internal medicine; Body weight","score_opus":0.04305196452338748,"score_gpt":0.34376366903967015,"score_spread":0.30071170451628265,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2996944597","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":[0.00007931399,0.9992124,0.000052005566,0.00014141417,0.00010071326,0.000006086578,0.000016499056,0.0000036306133,0.00038792615],"genre_scores_gemma":[0.00040977294,0.99908245,0.00012401781,0.0001352693,0.000090418165,0.000007714734,0.000021481952,8.008001e-7,0.000128046],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.9997378,0.0000480674,0.0000744207,0.0000394259,0.00007716523,0.000023177667],"domain_scores_gemma":[0.9993223,0.0004453369,0.0001127173,0.000011164197,0.00008183592,0.000026676442],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00064373994,0.0008515262,0.0012968273,0.0035105823,0.00030912337,0.0010182909,0.00090467907,0.001001324,0.0036875706],"category_scores_gemma":[0.001351523,0.00023052518,0.0009314518,0.0029027478,0.00033043866,0.0011170965,0.00060849887,0.0011043109,0.0008956489],"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":[0.00010353395,0.00007511366,0.00023327107,0.14183243,0.0002778306,0.00049724954,0.00014908903,0.00026862885,0.0010263801,0.002636387,0.026920648,0.8259795],"study_design_scores_gemma":[0.0000524577,0.00016573833,0.001694677,0.08526973,0.0014534736,0.004674412,0.00021076339,0.00015441883,0.0005288888,0.0019356597,0.9038149,0.00004482587],"about_ca_topic_score_codex":0.0010901734,"about_ca_topic_score_gemma":0.0020196482,"teacher_disagreement_score":0.0036875706,"about_ca_system_score_codex":0.00056557206,"about_ca_system_score_gemma":0.0015948762,"threshold_uncertainty_score":0.012336135},"labels":[],"label_agreement":null},{"id":"W2997229123","doi":"10.1002/wsbm.1476","title":"The evolution of genomic imprinting: Epigenetic control of mammary gland development and postnatal resource control","year":2019,"lang":"en","type":"review","venue":"WIREs Systems Biology and Medicine","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":19,"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; Medical Research Council Canada; Federation of European Biochemical Societies","keywords":"Genomic imprinting; Imprinting (psychology); Offspring; Biology; Epigenetics; Lactation; DNA methylation; Pregnancy; Endocrinology; Genetics; Gene; Gene expression","score_opus":0.012919201667696521,"score_gpt":0.26518524002958843,"score_spread":0.25226603836189193,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2997229123","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":[0.00013477246,0.99666566,0.000477793,0.00050631596,0.00039011615,0.0000027493393,0.000013346253,0.000012417732,0.0017968239],"genre_scores_gemma":[0.0014147508,0.99642557,0.00033741634,0.00024204097,0.0004407282,0.00000617394,0.000027242442,0.0000028752097,0.0011032091],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.9998173,0.000034393044,0.000019667597,0.000047430498,0.00006154292,0.000019687377],"domain_scores_gemma":[0.9996947,0.00014663493,0.00003671909,0.000014197165,0.00006969561,0.000038104037],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00046985014,0.00075793697,0.0009553026,0.0022412615,0.0003181096,0.0011742237,0.00095437065,0.0014942823,0.0023082418],"category_scores_gemma":[0.0006885812,0.00021168847,0.00029282767,0.0025973518,0.001304152,0.0017213419,0.00089298864,0.001823393,0.0017925866],"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":[0.000052110565,0.000028796745,0.00034873336,0.0052271206,0.00005025298,0.0003669577,0.000119754484,0.00046132566,0.0024189262,0.020626439,0.021477865,0.9488217],"study_design_scores_gemma":[0.00000614839,0.000039333736,0.0014199903,0.0016418053,0.000035860732,0.0022558467,0.0000837052,0.000113981034,0.0006700859,0.008558012,0.98515284,0.000022303564],"about_ca_topic_score_codex":0.0008707477,"about_ca_topic_score_gemma":0.000982124,"teacher_disagreement_score":0.0023082418,"about_ca_system_score_codex":0.0010979892,"about_ca_system_score_gemma":0.0009725305,"threshold_uncertainty_score":0.007966518},"labels":[],"label_agreement":null},{"id":"W2997372936","doi":"10.1558/jmbs.v1i2.11878","title":"Grammatical Gender in Atypical Language Development","year":2019,"lang":"en","type":"article","venue":"Journal of Monolingual and Bilingual Speech","topic":"Genetic Syndromes and Imprinting","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":"University of Ottawa","funders":"","keywords":"Neuroscience of multilingualism; Linguistics; Psychology; Grammatical gender; Noun; Sentence; Task (project management); Population; Preference; Typically developing; Developmental psychology; Sociology; Mathematics","score_opus":0.011580703515498798,"score_gpt":0.2640288862382522,"score_spread":0.25244818272275343,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2997372936","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.999037,0.000016670569,0.00014463415,0.000018448487,0.0000017661706,0.000003763051,0.000023847537,0.0000065101844,0.00074732304],"genre_scores_gemma":[0.99907506,0.000018247574,0.0005707833,0.00002337928,0.0000019126035,0.0000082708,0.00003927038,0.0000064526375,0.00025669855],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9995839,0.00008596151,0.000033812237,0.00012500708,0.0001260939,0.000045251385],"domain_scores_gemma":[0.99889576,0.00039872192,0.0002847755,0.00014837639,0.00013181487,0.00014049013],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0004012851,0.00041679078,0.0002748121,0.00068582396,0.0002789425,0.00060463016,0.0002746874,0.00039657255,0.0014328226],"category_scores_gemma":[0.0026475417,0.0001198005,0.00018281178,0.0002651547,0.0011231252,0.00048925256,0.0009247586,0.0003945873,0.0001792801],"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":[0.0008838934,0.00075218617,0.81412643,0.00012832395,0.000038564758,0.022226749,0.026937626,0.00063578936,0.07897009,0.004195996,0.00065344153,0.050450925],"study_design_scores_gemma":[0.00011919684,0.0024658951,0.88836944,0.000059614427,0.000076422366,0.05584355,0.016655155,0.005519231,0.01373665,0.012188675,0.00486939,0.000096757125],"about_ca_topic_score_codex":0.002700972,"about_ca_topic_score_gemma":0.0037586421,"teacher_disagreement_score":0.002700972,"about_ca_system_score_codex":0.00032066464,"about_ca_system_score_gemma":0.00032239748,"threshold_uncertainty_score":0.0053704977},"labels":[],"label_agreement":null},{"id":"W3000225091","doi":"10.1038/s41420-019-0235-x","title":"BORIS/CTCFL promotes a switch from a proliferative towards an invasive phenotype in melanoma cells","year":2020,"lang":"en","type":"article","venue":"Cell Death Discovery","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","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":"McGill University Health Centre; McGill University; Jewish General Hospital","funders":"Canadian Institutes of Health Research; McGill University; Israel Cancer Research Fund","keywords":"Reprogramming; Melanoma; Phenotype; Biology; Phenotypic switching; Cancer research; Transcriptome; Regulator; Cell biology; Gene expression; Genetics; Cell; Gene","score_opus":0.016438551772940478,"score_gpt":0.23310696395937022,"score_spread":0.21666841218642974,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W3000225091","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9955134,0.00048458594,0.0019227515,0.000062059065,0.00002456712,0.00001240204,0.00039440522,0.00010778877,0.0014781159],"genre_scores_gemma":[0.99588096,0.000199717,0.00074775657,0.00003908705,0.000004133365,0.0000118630605,0.0003852224,0.000016238557,0.002715097],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99993324,0.000007269421,0.00000410908,0.000015592688,0.000019034924,0.000020774247],"domain_scores_gemma":[0.99995685,0.000007624391,0.000010562065,0.0000049953173,0.0000040928176,0.000015830983],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00005156766,0.00016061318,0.00012232823,0.00013113405,0.00010140612,0.00017214476,0.00007326057,0.000120393466,0.0017540926],"category_scores_gemma":[0.00003455244,0.000095931566,0.00011589215,0.00008074026,0.00011978119,0.000073812094,0.00013287066,0.00032998846,0.0002990915],"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":[0.000018251569,0.0000050171284,0.00005939677,0.0000053052268,6.6820826e-7,0.000011968518,0.0000029412577,0.000010497269,0.9996779,0.00002517285,0.000011949836,0.00017101971],"study_design_scores_gemma":[0.000007629559,0.000110202025,0.005357032,0.000002195319,0.0000039877923,0.00008683446,0.000028505625,0.0008100159,0.9921245,0.000039167546,0.0014272952,0.0000025452744],"about_ca_topic_score_codex":0.00049730594,"about_ca_topic_score_gemma":0.000758567,"teacher_disagreement_score":0.0017540926,"about_ca_system_score_codex":0.00017242551,"about_ca_system_score_gemma":0.000088749744,"threshold_uncertainty_score":0.0058680773},"labels":[],"label_agreement":null},{"id":"W3001089571","doi":"10.1038/s41398-020-0720-2","title":"Translational outcomes in a full gene deletion of ubiquitin protein ligase E3A rat model of Angelman syndrome","year":2020,"lang":"en","type":"article","venue":"Translational Psychiatry","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":65,"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; Toronto Centre for Phenogenomics; Hospital for Sick Children","funders":"Eunice Kennedy Shriver National Institute of Child Health and Human Development; National Institutes of Health; National Institute of Neurological Disorders and Stroke; Foundation for Angelman Syndrome Therapeutics","keywords":"UBE3A; Angelman syndrome; Microcephaly; Intellectual disability; Ataxia; Neurodevelopmental disorder; Ubiquitin ligase; Genetics; Biology; Neuroscience; Psychology; Ubiquitin; Gene","score_opus":0.018486156859936896,"score_gpt":0.2455962153933495,"score_spread":0.2271100585334126,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W3001089571","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99310666,0.00050710316,0.0035612416,0.00021912769,0.00012837458,0.00008621982,0.0012640245,0.00027104758,0.0008562571],"genre_scores_gemma":[0.98572737,0.0006343434,0.004273467,0.00014488725,0.00002976458,0.000249936,0.0016209837,0.00008798583,0.007231266],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9995203,0.000059642534,0.000066159446,0.00013304959,0.00011100436,0.00010988505],"domain_scores_gemma":[0.99937564,0.000034324712,0.00021283705,0.00007893702,0.00005319734,0.00024497815],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00035352484,0.0014825361,0.0006004646,0.0014914086,0.00033624828,0.0003804889,0.0005233353,0.0007768565,0.0031843055],"category_scores_gemma":[0.00022866338,0.00037978985,0.00089692813,0.00033109583,0.0006697908,0.00041050246,0.0004674514,0.0015119417,0.0008711054],"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":[0.0006386808,0.00036216734,0.000537957,0.000039160972,0.000022371843,0.0003047125,0.00002646193,0.00012559556,0.99612147,0.0002604347,0.00012363339,0.0014373265],"study_design_scores_gemma":[0.00024538932,0.009003228,0.010613338,0.000033517197,0.00014148741,0.0025084517,0.00017412528,0.0021276725,0.9711463,0.00027240103,0.0036967164,0.00003739962],"about_ca_topic_score_codex":0.0011423287,"about_ca_topic_score_gemma":0.0015718761,"teacher_disagreement_score":0.0031843055,"about_ca_system_score_codex":0.0005808375,"about_ca_system_score_gemma":0.0005968858,"threshold_uncertainty_score":0.010652602},"labels":[],"label_agreement":null},{"id":"W3001510942","doi":"10.3390/genes11020128","title":"Prader–Willi-Like Phenotype Caused by an Atypical 15q11.2 Microdeletion","year":2020,"lang":"en","type":"article","venue":"Genes","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":46,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Stollery Children's Hospital; University of Saskatchewan; University of Alberta Hospital; University of Alberta","funders":"Canadian Institutes of Health Research; Alberta Innovates; W. Garfield Weston Foundation; BC Children's Hospital","keywords":"Exome sequencing; Phenotype; Genetics; Short stature; Biology; Phenocopy; Locus (genetics); Small nucleolar RNA; Hypotonia; Exome; Gene; Long non-coding RNA; Endocrinology; RNA","score_opus":0.015961166765606563,"score_gpt":0.2368240721635669,"score_spread":0.22086290539796033,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W3001510942","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99644166,0.00030021163,0.0016664687,0.00014576358,0.000034862023,0.000027236516,0.0002135945,0.00008393255,0.0010864006],"genre_scores_gemma":[0.9976393,0.00023294386,0.0012549157,0.000046417274,0.000046052977,0.000012554621,0.00012258317,0.000012521213,0.0006326867],"study_design_codex":"case_report","study_design_gemma":"case_report","domain_scores_codex":[0.9998085,0.000028972143,0.00001815716,0.00007443426,0.000032211094,0.000037858],"domain_scores_gemma":[0.99942136,0.00017168987,0.00020175331,0.000033485932,0.000018138606,0.0001536298],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00015221028,0.0009818035,0.00052872347,0.00081682915,0.0004371058,0.0002741479,0.0004546302,0.00070733385,0.00208186],"category_scores_gemma":[0.0008365621,0.00033999764,0.00029179288,0.0004613672,0.00078872044,0.00026351304,0.0007693318,0.0007525015,0.0004314974],"study_design_candidate":"case_report","study_design_consensus":"case_report","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0001719426,0.0000640071,0.0326458,0.00007465909,0.000054284,0.93562794,0.00036131535,0.00028662305,0.025396373,0.0006277228,0.0003808657,0.0043085054],"study_design_scores_gemma":[0.000034146873,0.00031808615,0.04694288,0.000011532337,0.000050965133,0.9447553,0.0001116382,0.00053530606,0.005560034,0.00023144086,0.0014258814,0.000022774657],"about_ca_topic_score_codex":0.0006765798,"about_ca_topic_score_gemma":0.0009270258,"teacher_disagreement_score":0.00208186,"about_ca_system_score_codex":0.00015921585,"about_ca_system_score_gemma":0.00019931326,"threshold_uncertainty_score":0.0069645643},"labels":[],"label_agreement":null},{"id":"W3003079370","doi":"10.3389/fendo.2019.00940","title":"Why and How Imprinted Genes Drive Fetal Programming","year":2020,"lang":"en","type":"article","venue":"Frontiers in Endocrinology","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","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","funders":"Natural Sciences and Engineering Research Council of Canada; Simon Fraser University","keywords":"Genomic imprinting; Offspring; Intrauterine growth restriction; Biology; Fetus; Disease; Imprinting (psychology); Endocrinology; Internal medicine; Gene; Bioinformatics; Pregnancy; Physiology; Genetics; Gene expression; Medicine; DNA methylation","score_opus":0.0096604366547733,"score_gpt":0.21931681166894307,"score_spread":0.20965637501416978,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W3003079370","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":[0.37028098,0.41092488,0.069763176,0.0585626,0.0020568257,0.00004802924,0.0009881994,0.0006379708,0.0867374],"genre_scores_gemma":[0.8516024,0.1271631,0.0081506455,0.0033577306,0.00086453307,0.000038137365,0.00015519267,0.000083756175,0.008584411],"study_design_codex":"theoretical_or_conceptual","study_design_gemma":"not_applicable","domain_scores_codex":[0.99970967,0.00007797084,0.0000161266,0.00007993032,0.000056303095,0.000060067377],"domain_scores_gemma":[0.9996131,0.00020665718,0.00007749947,0.000032219792,0.000035672427,0.000035002213],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0005080657,0.00018899233,0.00030229797,0.00028302614,0.00016733908,0.0010132008,0.00033937668,0.0006753255,0.0016025023],"category_scores_gemma":[0.0012407629,0.0001246176,0.00018791725,0.00022782186,0.001630669,0.001102557,0.00043076253,0.0007334603,0.00044112257],"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":[0.0005754803,0.00005064902,0.04143214,0.0016786143,0.00022734716,0.005021918,0.0016848283,0.0046840166,0.12524171,0.43559137,0.0105406465,0.37327126],"study_design_scores_gemma":[0.000059518996,0.00025717024,0.08920548,0.0009434289,0.00025954863,0.011317765,0.0022661707,0.0034657829,0.07795953,0.53003883,0.28410417,0.00012252074],"about_ca_topic_score_codex":0.00078402093,"about_ca_topic_score_gemma":0.00066645676,"teacher_disagreement_score":0.0016025023,"about_ca_system_score_codex":0.00050622533,"about_ca_system_score_gemma":0.0002897553,"threshold_uncertainty_score":0.0053609014},"labels":[],"label_agreement":null},{"id":"W3004450975","doi":"10.1016/j.molcel.2020.01.020","title":"Imprinted Maternally Expressed microRNAs Antagonize Paternally Driven Gene Programs in Neurons","year":2020,"lang":"en","type":"article","venue":"Molecular Cell","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":53,"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 General Medical Sciences; National Eye Institute; National Institutes of Health; National Cancer Institute; Fonds de Recherche du Québec - Santé; Natural Sciences and Engineering Research Council of Canada","keywords":"Biology; Genomic imprinting; microRNA; Gene silencing; Genetics; Gene; Regulation of gene expression; Gene expression; Gene cluster; Psychological repression; DNA methylation","score_opus":0.013404715163751761,"score_gpt":0.20686282610414045,"score_spread":0.19345811094038867,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W3004450975","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.98364604,0.0015578505,0.0087351715,0.00020438588,0.000121007804,0.000009752267,0.00012420985,0.00018297635,0.0054186885],"genre_scores_gemma":[0.9946089,0.00036815356,0.0018792222,0.00004822078,0.000010683601,0.000007758777,0.000050471175,0.000054067325,0.0029725365],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9997371,0.000049269795,0.000023039494,0.000044524964,0.00008772559,0.00005845066],"domain_scores_gemma":[0.99975604,0.00006958332,0.000061217324,0.00003327078,0.00002171932,0.000058165555],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0002306538,0.00031229472,0.00024513985,0.00032928452,0.00015642398,0.00045162177,0.00051690993,0.00031403624,0.0014346582],"category_scores_gemma":[0.00032269207,0.0002717185,0.00017715665,0.00012995597,0.00043499173,0.00030701366,0.0005009054,0.0005088494,0.00039001522],"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":[0.00008567057,0.000004558262,0.00030891525,0.0000110507945,0.000004410248,0.00017755521,0.000014281207,0.000084090185,0.9968917,0.0012746698,0.000037016216,0.0011061149],"study_design_scores_gemma":[0.000014299312,0.000044991244,0.004436604,0.0000036152428,0.000011278371,0.0005029748,0.000038138667,0.0008097456,0.9924793,0.00033300798,0.0013221513,0.0000039013785],"about_ca_topic_score_codex":0.00050600903,"about_ca_topic_score_gemma":0.0019785564,"teacher_disagreement_score":0.0014346582,"about_ca_system_score_codex":0.0004643748,"about_ca_system_score_gemma":0.0003268459,"threshold_uncertainty_score":0.004799366},"labels":[],"label_agreement":null},{"id":"W3005197391","doi":"10.1016/j.psychres.2020.112858","title":"Does SNORD116 mediate aspects of psychosis in Prader-Willi syndrome? Evidence from a non-clinical population","year":2020,"lang":"en","type":"article","venue":"Psychiatry Research","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":7,"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; Simon Fraser University","funders":"Natural Sciences and Engineering Research Council of Canada","keywords":"Epigenetics; Genetics; Locus (genetics); Psychosis; Biology; Autism; Phenotype; Genomic imprinting; Population; Single-nucleotide polymorphism; Haplotype; Gene; Allele; Psychology; Gene expression; DNA methylation; Genotype; Developmental psychology; Medicine; Psychiatry","score_opus":0.08071746153591641,"score_gpt":0.40203637846510015,"score_spread":0.32131891692918374,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W3005197391","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99687445,0.000544169,0.00022743875,0.0002110914,0.000014720212,0.000010366162,0.00022030315,0.000005855391,0.0018915591],"genre_scores_gemma":[0.99881977,0.00028876457,0.00010567621,0.000058168473,0.000015438074,0.000007056259,0.00013440088,0.000006396345,0.00056423165],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99940324,0.00022598704,0.00004580892,0.00014477798,0.00010037347,0.00007976192],"domain_scores_gemma":[0.9985544,0.00064399856,0.0003290241,0.00020980886,0.00009592677,0.00016682352],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0008107376,0.00071956107,0.0004893454,0.00083554315,0.0008539692,0.00080219365,0.0009151489,0.0009924013,0.0061194333],"category_scores_gemma":[0.0035251435,0.00030109304,0.0004101342,0.0006847298,0.0012088727,0.0005035767,0.00074683316,0.00048830285,0.0004555725],"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":[0.0068573044,0.00037756923,0.90591395,0.00016784853,0.00085745536,0.010893777,0.002871772,0.00022266261,0.049600847,0.002708295,0.0006685962,0.018859971],"study_design_scores_gemma":[0.00027933434,0.0010133443,0.9778217,0.00006109196,0.0005653649,0.009000936,0.0015959362,0.00043836213,0.004621775,0.00231192,0.0022596938,0.000030566687],"about_ca_topic_score_codex":0.004279505,"about_ca_topic_score_gemma":0.002941649,"teacher_disagreement_score":0.0061194333,"about_ca_system_score_codex":0.00018958579,"about_ca_system_score_gemma":0.00029266186,"threshold_uncertainty_score":0.020471513},"labels":[],"label_agreement":null},{"id":"W3006415667","doi":"10.1186/s12863-020-0809-x","title":"The effects of the DNA Demethylating reagent, 5-azacytidine on SMCHD1 genomic localization","year":2020,"lang":"en","type":"article","venue":"BMC Genetics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":4,"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":"Natural Sciences and Engineering Research Council of Canada","keywords":"DNA methylation; Biology; Chromatin; Epigenetics; RNA-Directed DNA Methylation; Genomic imprinting; Genetics; Epigenomics; Gene; Methylation; Molecular biology; Gene expression","score_opus":0.01324606570476634,"score_gpt":0.22662208433280492,"score_spread":0.2133760186280386,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W3006415667","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9865124,0.007275084,0.0022974696,0.00013494109,0.00006960403,0.00002565874,0.00075630547,0.00008049697,0.0028480487],"genre_scores_gemma":[0.99085546,0.002579067,0.0028731497,0.00006370453,0.000010534736,0.00002669609,0.0011051329,0.000014396545,0.002471904],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9998534,0.000024284293,0.00001318662,0.000042977157,0.000041174815,0.000024989631],"domain_scores_gemma":[0.9998934,0.000042271495,0.000015714386,0.000013588843,0.000017851758,0.000017047445],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00016175481,0.0001860733,0.00023944474,0.00013860929,0.0001941156,0.00017998372,0.00017984923,0.00023761035,0.0015077643],"category_scores_gemma":[0.00014286372,0.00013242202,0.00018864954,0.00018504322,0.00019404269,0.00011479284,0.00010669266,0.00049202895,0.0002682454],"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":[0.0001598536,0.00001697683,0.00031215363,0.00004689689,0.000008415859,0.00002394535,0.000023780427,0.00004828719,0.9978421,0.000030497797,0.000032674925,0.001454386],"study_design_scores_gemma":[0.000006345243,0.00022355898,0.0058825654,0.0000046333007,0.000017941218,0.00006647885,0.000027178701,0.00037770288,0.9918858,0.00001697609,0.0014875956,0.0000031508803],"about_ca_topic_score_codex":0.0024942043,"about_ca_topic_score_gemma":0.0051298654,"teacher_disagreement_score":0.0024942043,"about_ca_system_score_codex":0.00033726808,"about_ca_system_score_gemma":0.00022711697,"threshold_uncertainty_score":0.0050439835},"labels":[],"label_agreement":null},{"id":"W3010580726","doi":"10.1016/j.physbeh.2020.112864","title":"Disentangling ingestive behavior-related phenotypes in Prader–Willi syndrome: Integrating information from nonclinical studies and clinical trials to better understand the pathophysiology of hyperphagia and obesity","year":2020,"lang":"en","type":"review","venue":"Physiology & Behavior","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":4,"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","funders":"Canadian Institutes of Health Research","keywords":"Obesity; Medicine; Phenotype; Clinical trial; Endocrine system; Bioinformatics; Candidate gene; Animal studies; Gene; Internal medicine; Biology; Genetics; Hormone","score_opus":0.10035659614918822,"score_gpt":0.41738866921887036,"score_spread":0.3170320730696821,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W3010580726","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":[0.00005168535,0.9993445,0.000099891266,0.00016891822,0.00010365743,0.0000027509855,0.000016153412,0.000004556401,0.00020785858],"genre_scores_gemma":[0.00033130558,0.99882764,0.0002248573,0.0002016375,0.00017839031,0.000005459316,0.000034726007,0.0000013544441,0.00019463565],"study_design_codex":"design_other","study_design_gemma":"systematic_review","domain_scores_codex":[0.9997987,0.00004315823,0.000034245124,0.00003700144,0.000072319526,0.000014582339],"domain_scores_gemma":[0.9993819,0.00040320453,0.00006263258,0.000012567774,0.00009687762,0.000042792355],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0010176842,0.0012526858,0.0025822646,0.0017769379,0.0001505107,0.0009853288,0.0010357596,0.0011485049,0.0023417738],"category_scores_gemma":[0.0010791466,0.0002617128,0.00059077574,0.0015340267,0.00048561962,0.0010754341,0.0006532628,0.00228495,0.0012101001],"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":[0.00016865849,0.00006387364,0.00029470667,0.013932014,0.000246762,0.00025217741,0.000025982867,0.00030469327,0.001227825,0.0019758742,0.02187833,0.9596292],"study_design_scores_gemma":[0.00018556,0.00022181276,0.003389689,0.009280978,0.00093320245,0.0026418115,0.00009240907,0.00024021333,0.0006591736,0.0049423287,0.9773516,0.00006121115],"about_ca_topic_score_codex":0.0011293079,"about_ca_topic_score_gemma":0.0027861055,"teacher_disagreement_score":0.0025822646,"about_ca_system_score_codex":0.00051787973,"about_ca_system_score_gemma":0.0009974954,"threshold_uncertainty_score":0.007834017},"labels":[],"label_agreement":null},{"id":"W3014418129","doi":"10.1089/biores.2020.0004","title":"Klotho Pathways, Myelination Disorders, Neurodegenerative Diseases, and Epigenetic Drugs","year":2020,"lang":"en","type":"review","venue":"BioResearch open access","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":35,"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 Eye Institute","keywords":"Klotho; Remyelination; Neuroscience; Medicine; Myelin; Disease; Bioinformatics; Central nervous system; Biology; Internal medicine","score_opus":0.09038504095882766,"score_gpt":0.42740823788262605,"score_spread":0.3370231969237984,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W3014418129","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":[0.00009752004,0.9962991,0.0001360821,0.00047941436,0.00043823002,0.0000031809798,0.00001625931,0.000016344708,0.0025138748],"genre_scores_gemma":[0.00083417696,0.99562246,0.00018777461,0.0003610397,0.00039123982,0.0000064982187,0.00003650509,0.0000037075097,0.0025566039],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.99983656,0.000026829946,0.000015706331,0.000027227024,0.00007238713,0.000021303707],"domain_scores_gemma":[0.9997484,0.00012113324,0.000025548057,0.000011811584,0.00005603877,0.000037074067],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00046623193,0.0008437298,0.00090201857,0.0022701123,0.0004067811,0.001193002,0.0007784813,0.0011944023,0.006855147],"category_scores_gemma":[0.0007024947,0.00019647392,0.0003642567,0.0020994933,0.00083724514,0.0015545401,0.0009945001,0.002180985,0.0033650643],"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":[0.00006755474,0.00008237245,0.00015281036,0.0077517894,0.00004703599,0.0002992555,0.00009571232,0.00025917776,0.0023608871,0.012873575,0.05755432,0.91845554],"study_design_scores_gemma":[0.0000050789977,0.000027612701,0.000249296,0.0010359791,0.00002152178,0.000636494,0.00003690248,0.000029599676,0.00034502815,0.0029135942,0.99469143,0.000007549022],"about_ca_topic_score_codex":0.000992399,"about_ca_topic_score_gemma":0.0023502212,"teacher_disagreement_score":0.006855147,"about_ca_system_score_codex":0.0007805203,"about_ca_system_score_gemma":0.00086194597,"threshold_uncertainty_score":0.022932768},"labels":[],"label_agreement":null},{"id":"W3019737162","doi":"10.1371/journal.pgen.1008709","title":"Placental imprinting: Emerging mechanisms and functions","year":2020,"lang":"en","type":"review","venue":"PLoS Genetics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":81,"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":"Alberta Children's Hospital Research Institute; BC Children's Hospital","keywords":"Placentation; Biology; Imprinting (psychology); Epigenome; Genomic imprinting; Placenta; Trophoblast; Epigenetics; Epigenesis; Pregnancy; Genetics; Bioinformatics; Evolutionary biology; Cell biology; DNA methylation; Gene; Fetus; Gene expression","score_opus":0.029202394456767252,"score_gpt":0.2746002806374351,"score_spread":0.24539788618066782,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W3019737162","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":[0.00007264578,0.99852824,0.00013913997,0.00030439344,0.00013601845,0.0000014098217,0.000013571596,0.000007238509,0.0007973083],"genre_scores_gemma":[0.00060793554,0.99864584,0.00012921795,0.00012424328,0.00014359242,0.0000032090759,0.000019594167,0.0000014515624,0.00032489852],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.9998659,0.00002827576,0.00001742933,0.000025229936,0.00004431574,0.00001884657],"domain_scores_gemma":[0.9997532,0.00013393442,0.000024681796,0.000009157408,0.00004600177,0.000033083375],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0006312248,0.0007766063,0.0010638331,0.0014818014,0.00022269264,0.0013513814,0.0009318019,0.0009419314,0.0033265515],"category_scores_gemma":[0.00074287417,0.00020452192,0.000285632,0.0016642191,0.00084276235,0.0015304696,0.0009510326,0.0015543692,0.001861752],"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":[0.00007745516,0.000023873516,0.00022532666,0.011961236,0.00007263316,0.00036711444,0.00009232566,0.000416756,0.002725851,0.015838835,0.023061637,0.9451368],"study_design_scores_gemma":[0.000008814832,0.000036168112,0.00064706337,0.0019742395,0.000054520995,0.0012092552,0.00006828885,0.000075968994,0.00050327,0.0055523687,0.9898537,0.000016307018],"about_ca_topic_score_codex":0.0006780292,"about_ca_topic_score_gemma":0.0008967372,"teacher_disagreement_score":0.0033265515,"about_ca_system_score_codex":0.00073400507,"about_ca_system_score_gemma":0.0010522442,"threshold_uncertainty_score":0.011128485},"labels":[],"label_agreement":null},{"id":"W3029749726","doi":"10.1111/gbb.12679","title":"Mice lacking paternal expression of imprinted <i>Grb10</i> are risk‐takers","year":2020,"lang":"en","type":"article","venue":"Genes Brain & Behavior","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":18,"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; Leverhulme Trust; Medical Research Council Canada; Wellcome Trust","keywords":"Task (project management); Reinforcement; Genomic imprinting; Psychology; Developmental psychology; Social psychology; Biology; Genetics; Gene; Gene expression; Economics","score_opus":0.01825033895365077,"score_gpt":0.2499651888315403,"score_spread":0.23171484987788954,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W3029749726","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9925092,0.00017874858,0.00428889,0.00017492156,0.00005236693,0.000020838472,0.0013144333,0.00037620752,0.0010843314],"genre_scores_gemma":[0.98610467,0.0003662984,0.004441641,0.00017434644,0.0000341378,0.00007441846,0.00120514,0.00042322755,0.007176126],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9995466,0.00006148596,0.00005900772,0.00012665044,0.00012248193,0.00008381619],"domain_scores_gemma":[0.99864787,0.0002045987,0.00062301895,0.00011490484,0.00004662862,0.00036297148],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00025505043,0.0010037012,0.00037858973,0.0012636532,0.00020272216,0.0005273434,0.00048388942,0.0006879531,0.0061555617],"category_scores_gemma":[0.00026416982,0.00044842798,0.000423945,0.00028882912,0.000980167,0.00032821138,0.0004504897,0.0016554332,0.0010907806],"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":[0.00035559744,0.00008766508,0.0014521409,0.000023762927,0.000025535846,0.00039202228,0.000029014578,0.00013202954,0.99605465,0.00019082334,0.00010097794,0.0011558242],"study_design_scores_gemma":[0.00022791186,0.0013392543,0.061836477,0.000048771682,0.00016270007,0.006246396,0.00035728706,0.0034867304,0.9216415,0.0005296333,0.004048242,0.000075115364],"about_ca_topic_score_codex":0.00081004837,"about_ca_topic_score_gemma":0.0011868994,"teacher_disagreement_score":0.0061555617,"about_ca_system_score_codex":0.00019563161,"about_ca_system_score_gemma":0.00014576121,"threshold_uncertainty_score":0.020592391},"labels":[],"label_agreement":null},{"id":"W3030349097","doi":"10.1097/md.0000000000019965","title":"Identification of a novel mutation in pseudohypoparathyroidism type Ia in a Chinese family","year":2020,"lang":"en","type":"article","venue":"Medicine","topic":"Genetic Syndromes and Imprinting","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":"Artificial Intelligence in Medicine (Canada)","funders":"","keywords":"GNAS complex locus; Pseudohypoparathyroidism; Medicine; Endocrinology; Internal medicine; Brachydactyly; Parathyroid hormone; Short stature; Hypoparathyroidism; Genetics; Gene; Biology; Calcium","score_opus":0.018241394745705165,"score_gpt":0.29234828736636614,"score_spread":0.27410689262066096,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W3030349097","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9969398,0.00035318328,0.0007427504,0.00039774994,0.00003586659,0.000038401075,0.00014518894,0.00002842459,0.0013186814],"genre_scores_gemma":[0.99840313,0.00021593718,0.00052988157,0.00012402039,0.00003828392,0.000014431118,0.000077466444,0.0000087331455,0.0005880901],"study_design_codex":"case_report","study_design_gemma":"observational","domain_scores_codex":[0.9997726,0.00001568313,0.000028049995,0.000096447104,0.000038316328,0.00004902851],"domain_scores_gemma":[0.9997117,0.000083560575,0.000054699794,0.000018382205,0.000029783132,0.00010189625],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00017621726,0.00093664957,0.00041497586,0.0013295581,0.0014765904,0.00030256814,0.000700092,0.0011772178,0.0027119224],"category_scores_gemma":[0.0007097705,0.0003105507,0.00068880233,0.00091200054,0.0007441385,0.00031520243,0.00051857403,0.0006217779,0.00025225335],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.000070634334,0.000059723527,0.054324426,0.0000653401,0.000032297146,0.9198594,0.0014101602,0.00014961862,0.018733239,0.0003482101,0.00035952055,0.004587392],"study_design_scores_gemma":[0.000029199247,0.00019068267,0.09618274,0.000030607083,0.00007270677,0.8965323,0.0005320842,0.0006887957,0.0036088666,0.0001966506,0.0019073259,0.000028106495],"about_ca_topic_score_codex":0.008645629,"about_ca_topic_score_gemma":0.005566801,"teacher_disagreement_score":0.008645629,"about_ca_system_score_codex":0.0005599294,"about_ca_system_score_gemma":0.0007454246,"threshold_uncertainty_score":0.017190576},"labels":[],"label_agreement":null},{"id":"W3035437525","doi":"10.1007/s00439-020-02193-9","title":"The necdin interactome: evaluating the effects of amino acid substitutions and cell stress using proximity-dependent biotinylation (BioID) and mass spectrometry","year":2020,"lang":"en","type":"article","venue":"Human Genetics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":4,"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","funders":"Canadian Institutes of Health Research","keywords":"Interactome; Biology; Protein–protein interaction; Biotinylation; PRC2; Gene; Ubiquitin ligase; Ubiquitin; Genetics; Loss function; Cell biology; Computational biology; Molecular biology; Epigenetics; Phenotype; Histone H3","score_opus":0.027086289820761538,"score_gpt":0.28755874619843247,"score_spread":0.2604724563776709,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W3035437525","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9734813,0.0014870544,0.021051904,0.00027694946,0.00004780074,0.00008280443,0.001578177,0.00020085557,0.0017931947],"genre_scores_gemma":[0.95634013,0.0014771675,0.03471401,0.00031490656,0.000014053352,0.00017060996,0.0027310953,0.000131712,0.0041063316],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9995234,0.000070893635,0.000031888903,0.00012519972,0.00018502153,0.00006350897],"domain_scores_gemma":[0.99963915,0.00011158363,0.00009007967,0.000039102844,0.00005715823,0.000062899235],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00054789847,0.000484226,0.00047683163,0.0004480772,0.000502128,0.0005166597,0.0003666093,0.00057952304,0.0015344766],"category_scores_gemma":[0.00059923937,0.00024049148,0.00033689404,0.0004316237,0.00034926858,0.0003443906,0.00052258634,0.0007077749,0.00044018083],"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":[0.00013756093,0.000010731237,0.0004354943,0.0000331005,0.000012364507,0.00003473249,0.000015932417,0.000042070267,0.99847597,0.000042535212,0.000027561295,0.0007318962],"study_design_scores_gemma":[0.000008917333,0.00009799833,0.010523653,0.000004054224,0.00002436377,0.00028863695,0.00003873564,0.0020309708,0.9853007,0.000056644218,0.0016173705,0.00000804183],"about_ca_topic_score_codex":0.0014714104,"about_ca_topic_score_gemma":0.0032844485,"teacher_disagreement_score":0.0015344766,"about_ca_system_score_codex":0.00058679195,"about_ca_system_score_gemma":0.00024258114,"threshold_uncertainty_score":0.005133271},"labels":[],"label_agreement":null},{"id":"W3041261123","doi":"10.1002/ajmg.a.61740","title":"A novel intronic variant in <scp><i>UBE3A</i></scp> identified by genome sequencing in a patient with an atypical presentation of Angelman syndrome","year":2020,"lang":"en","type":"article","venue":"American Journal of Medical Genetics Part A","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","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":"University of Toronto; Children's Hospital of Eastern Ontario; SickKids Foundation; Hospital for Sick Children","funders":"Canadian Institutes of Health Research","keywords":"Angelman syndrome; UBE3A; Genetics; Neurodevelopmental disorder; Biology; RNA splicing; Allele; Genetic testing; Presentation (obstetrics); RNA; Medicine; Gene","score_opus":0.012480952546646067,"score_gpt":0.24690597599017483,"score_spread":0.23442502344352875,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W3041261123","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99716777,0.00017664745,0.0010975614,0.0003268514,0.000037407088,0.000016300435,0.0001364302,0.000048810332,0.0009921965],"genre_scores_gemma":[0.9983608,0.00007473924,0.0008791089,0.00014709965,0.000040393617,0.000004743886,0.00006228894,0.000014446423,0.00041643373],"study_design_codex":"case_report","study_design_gemma":"case_report","domain_scores_codex":[0.99984896,0.000014599658,0.000013829087,0.00005518825,0.000033684464,0.000033717086],"domain_scores_gemma":[0.9994635,0.00019539525,0.00014758395,0.000018473635,0.00003178498,0.00014323942],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00011301464,0.00065409014,0.00030084458,0.0006881547,0.00048586202,0.00033308915,0.00036180625,0.0011646876,0.0010241341],"category_scores_gemma":[0.00091166166,0.00021223919,0.00035537902,0.0004263064,0.0005623474,0.00024419135,0.0002778762,0.00079728244,0.00025726066],"study_design_candidate":"case_report","study_design_consensus":"case_report","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00014021122,0.0000662539,0.038521364,0.000029458311,0.000019932548,0.9192692,0.000578464,0.00023314479,0.034828227,0.00044259313,0.00054580113,0.0053253695],"study_design_scores_gemma":[0.00002142197,0.00023063978,0.058380365,0.000010957676,0.000032324995,0.9320887,0.0001413075,0.0009459712,0.0069555915,0.00023344664,0.0009387689,0.000020394586],"about_ca_topic_score_codex":0.0019378267,"about_ca_topic_score_gemma":0.002044746,"teacher_disagreement_score":0.0019378267,"about_ca_system_score_codex":0.00030813355,"about_ca_system_score_gemma":0.000237221,"threshold_uncertainty_score":0.0038530827},"labels":[],"label_agreement":null},{"id":"W3041895066","doi":"10.1111/cen.14279","title":"Dietary macronutrient regulation of acyl and desacyl ghrelin concentrations in children with Prader‐Willi syndrome (PWS)","year":2020,"lang":"en","type":"article","venue":"Clinical Endocrinology","topic":"Genetic Syndromes and Imprinting","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":"University of Alberta Hospital; University of Alberta","funders":"","keywords":"Internal medicine; Endocrinology; Ghrelin; Orexigenic; Appetite; Medicine; Meal; Insulin; Hormone; Neuropeptide Y receptor; Receptor; Neuropeptide","score_opus":0.027591795270119828,"score_gpt":0.29000655695067773,"score_spread":0.2624147616805579,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W3041895066","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9997657,0.00010291442,0.000026894058,0.000009856976,0.000001785953,0.0000046385853,0.000053109805,0.0000017336419,0.0000333769],"genre_scores_gemma":[0.99919087,0.00021987762,0.00029983424,0.00002238371,0.0000034962895,0.000021732145,0.00014767588,0.0000017723859,0.00009238536],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9997677,0.00006732701,0.000024756626,0.00005483459,0.000050710172,0.000034722278],"domain_scores_gemma":[0.9995246,0.0001231358,0.00022373568,0.00002076724,0.000030740914,0.00007697121],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0004107581,0.00046864495,0.00037503635,0.00037220278,0.00020209745,0.00024404265,0.00016750574,0.00029098056,0.0010862579],"category_scores_gemma":[0.0009767471,0.0002695285,0.00032707187,0.00029186354,0.0005032888,0.0002482436,0.00034000108,0.0003868522,0.00011558623],"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":[0.005055099,0.0005870656,0.9606589,0.0001622195,0.00022440519,0.0008226904,0.00039952164,0.00022354694,0.023012415,0.000050717965,0.00017838566,0.00862494],"study_design_scores_gemma":[0.00006426313,0.0014035212,0.9966168,0.000007951492,0.000045566074,0.00060733187,0.00018597704,0.00009161346,0.0008519572,0.000016635211,0.00010425365,0.0000041703047],"about_ca_topic_score_codex":0.0035764277,"about_ca_topic_score_gemma":0.0037808479,"teacher_disagreement_score":0.0035764277,"about_ca_system_score_codex":0.0003275565,"about_ca_system_score_gemma":0.0002641474,"threshold_uncertainty_score":0.0071111917},"labels":[],"label_agreement":null},{"id":"W3047935522","doi":"10.3390/genes11080904","title":"The Gut Microbiota Profile in Children with Prader–Willi Syndrome","year":2020,"lang":"en","type":"article","venue":"Genes","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","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":"University of Alberta","funders":"W. Garfield Weston Foundation; Children's Health Research Institute; Women and Children's Health Research Institute; Foundation for Prader-Willi Research","keywords":"Biology; Feces; Gut flora; Microbiome; Metagenomics; Disease; Zoology; Microbiology; Physiology; Immunology; Genetics; Internal medicine; Medicine; Gene","score_opus":0.006564377946100264,"score_gpt":0.19878761642997406,"score_spread":0.1922232384838738,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W3047935522","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9995258,0.00021476559,0.000045574037,0.000014643793,0.0000021254443,0.0000031114394,0.00011229409,0.0000024807246,0.000079207544],"genre_scores_gemma":[0.99920267,0.00033158838,0.00016034351,0.000019741887,0.0000040697746,0.000006355634,0.00017787857,0.0000026277394,0.00009484288],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99969566,0.000055904453,0.000031575357,0.00009702242,0.00006929927,0.00005052237],"domain_scores_gemma":[0.99964595,0.000060776772,0.00016126335,0.000018336525,0.00003485533,0.00007892607],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00023979544,0.0004848024,0.00047882643,0.0010904886,0.0003779343,0.00044068522,0.00013922325,0.00031728216,0.0009000645],"category_scores_gemma":[0.0010784058,0.00028074955,0.00030498582,0.0006870028,0.00037946017,0.00033507848,0.00050866924,0.0004067124,0.00013307619],"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":[0.00016655655,0.000027277107,0.9922924,0.0000248021,0.00003928518,0.00082944543,0.00027080104,0.00003971556,0.0036058773,0.0000190357,0.000060078095,0.002624793],"study_design_scores_gemma":[0.0000028903112,0.00012681914,0.99726605,0.000008077642,0.000017248052,0.0019510627,0.00025685423,0.00004481106,0.00020529905,0.000013281062,0.00010423257,0.000003394183],"about_ca_topic_score_codex":0.0044788243,"about_ca_topic_score_gemma":0.0033991055,"teacher_disagreement_score":0.0044788243,"about_ca_system_score_codex":0.00028952802,"about_ca_system_score_gemma":0.00020732965,"threshold_uncertainty_score":0.00890547},"labels":[],"label_agreement":null},{"id":"W3080176413","doi":"10.3390/genes11090984","title":"A 24-Week Physical Activity Intervention Increases Bone Mineral Content without Changes in Bone Markers in Youth with PWS","year":2020,"lang":"en","type":"article","venue":"Genes","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":11,"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":"Medical Research and Materiel Command","keywords":"Medicine; Bone mineral; Bone mineral content; Internal medicine; Bone remodeling; Endocrinology; N-terminal telopeptide; Bone density; Alkaline phosphatase; Osteoporosis; Osteocalcin; Chemistry; Enzyme","score_opus":0.03726872326891207,"score_gpt":0.24791540877408969,"score_spread":0.21064668550517762,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W3080176413","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9997867,0.00007530048,0.000024750934,0.000010868151,0.0000045097586,0.00000882143,0.000012902065,0.0000022494573,0.0000739415],"genre_scores_gemma":[0.9994004,0.00013853097,0.00013850165,0.00002310852,0.000007255479,0.000023438894,0.000053090396,9.417379e-7,0.00021481076],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9998822,0.000029864987,0.000011265237,0.000019491297,0.000024713438,0.00003244835],"domain_scores_gemma":[0.9998828,0.0000151425575,0.00002677651,0.000005381438,0.0000117426225,0.000058011934],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0002060856,0.00020076054,0.00035948842,0.00015041616,0.00014565354,0.00014986741,0.00010491548,0.00015477945,0.0009791818],"category_scores_gemma":[0.00035133644,0.00009864291,0.00024609413,0.00010315601,0.00013298841,0.00011002461,0.00029425803,0.000256774,0.00011790627],"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":[0.026279831,0.023024866,0.6299162,0.0005937641,0.0005618457,0.00062704785,0.0013060588,0.00031154274,0.06624425,0.00010194228,0.0010658195,0.24996682],"study_design_scores_gemma":[0.00070639345,0.03440494,0.96104026,0.000041205196,0.00012156031,0.0002589145,0.0005343031,0.00027897465,0.0020417417,0.000026598442,0.00053907046,0.0000059925396],"about_ca_topic_score_codex":0.0013001381,"about_ca_topic_score_gemma":0.002679507,"teacher_disagreement_score":0.0013001381,"about_ca_system_score_codex":0.000095328425,"about_ca_system_score_gemma":0.00019171974,"threshold_uncertainty_score":0.0032756925},"labels":[],"label_agreement":null},{"id":"W3087985205","doi":"10.1016/j.theriogenology.2020.09.027","title":"Specific imprinted genes demethylation in association with oocyte donor’s age and culture conditions in bovine embryos assessed at day 7 and 12 post insemination","year":2020,"lang":"en","type":"article","venue":"Theriogenology","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":13,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"L'Alliance Boviteq; Université Laval","funders":"Fonds de recherche du Québec – Nature et technologies; Natural Sciences and Engineering Research Council of Canada; Fiona Stanley Hospital; Lyda Hill Foundation","keywords":"Genomic imprinting; Andrology; Biology; Oocyte; Embryo; Embryo culture; Insemination; Embryogenesis; Methylation; Estrous cycle; Human fertilization; DNA methylation; Genetics; Endocrinology; Gene expression; Gene; Pregnancy; Medicine","score_opus":0.010519241186511614,"score_gpt":0.22725927063183748,"score_spread":0.21674002944532586,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W3087985205","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9976786,0.0011147148,0.00024068516,0.000016943353,0.000008941583,0.000003649512,0.00027697434,0.000004864302,0.00065455213],"genre_scores_gemma":[0.99689025,0.00039366205,0.00020387121,0.000017427945,0.0000030079536,0.000010756457,0.00032137774,0.0000040726654,0.0021556588],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9999033,0.000011475688,0.000007476579,0.000033614444,0.000019405166,0.000024691413],"domain_scores_gemma":[0.9998678,0.000033512297,0.000040158648,0.000009548763,0.000023749097,0.000025292526],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00015178794,0.00009762925,0.0001907617,0.00022428032,0.00013379572,0.0002475454,0.00012310217,0.000117177275,0.0015446093],"category_scores_gemma":[0.0002291667,0.00011456266,0.000130788,0.00018848215,0.00013879036,0.00014040271,0.00014305879,0.0002709874,0.00018228228],"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":[0.0012335526,0.00003649582,0.023468286,0.00004488446,0.000017060445,0.00011531599,0.0002879442,0.000047754434,0.97135645,0.000102078506,0.000058458198,0.003231766],"study_design_scores_gemma":[0.000012589495,0.00050959236,0.73094356,0.000012810539,0.00004614154,0.00035366195,0.00058555027,0.00030627387,0.26496017,0.00008897103,0.002167308,0.000013297308],"about_ca_topic_score_codex":0.0020734763,"about_ca_topic_score_gemma":0.0043810867,"teacher_disagreement_score":0.0020734763,"about_ca_system_score_codex":0.00021263458,"about_ca_system_score_gemma":0.00015729251,"threshold_uncertainty_score":0.0051671863},"labels":[],"label_agreement":null},{"id":"W3088182247","doi":"10.1016/j.neuron.2020.08.023","title":"Parental Bias Has Benefits","year":2020,"lang":"en","type":"letter","venue":"Neuron","topic":"Genetic Syndromes and Imprinting","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":"University of Toronto","funders":"","keywords":"Homogeneous; Biology; Psychology; Neuroscience; Expression (computer science); Evolutionary biology; Developmental psychology; Genetics; Computer science","score_opus":0.046770615314432544,"score_gpt":0.23405310633725476,"score_spread":0.1872824910228222,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W3088182247","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":[0.0010348773,0.00349557,0.00018623217,0.9687858,0.013134705,0.0000035847138,0.000018757604,0.000023398912,0.0133169675],"genre_scores_gemma":[0.024960153,0.0025031047,0.00023623314,0.9216004,0.02911489,0.00001705485,0.000019520614,0.000024508747,0.021524182],"study_design_codex":"not_applicable","study_design_gemma":"theoretical_or_conceptual","domain_scores_codex":[0.99829084,0.00040626386,0.000104397106,0.00032149276,0.00055442686,0.00032256855],"domain_scores_gemma":[0.9942622,0.0031412337,0.000271561,0.00051445013,0.0006457843,0.0011648999],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0027976087,0.00048081417,0.0008587685,0.0003008245,0.0032157197,0.0025223081,0.0013369756,0.040122,0.008386495],"category_scores_gemma":[0.014911406,0.00029199908,0.0006757099,0.0002617148,0.005944046,0.002044241,0.0022631309,0.026660388,0.0032941347],"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":[0.00015633034,0.00004076079,0.001689202,0.00007644982,0.000067364505,0.007744034,0.00029800084,0.00014132795,0.000627682,0.076456055,0.8839981,0.028704597],"study_design_scores_gemma":[0.00013935029,0.000050536084,0.0017380612,0.0001744597,0.000034805526,0.006322773,0.00039379357,0.00023660129,0.00036945796,0.07391926,0.9165805,0.000040408166],"about_ca_topic_score_codex":0.004489712,"about_ca_topic_score_gemma":0.013564607,"teacher_disagreement_score":0.040122,"about_ca_system_score_codex":0.0026756972,"about_ca_system_score_gemma":0.0024488077,"threshold_uncertainty_score":0.028055608},"labels":[],"label_agreement":null},{"id":"W3089698622","doi":"10.1108/amhid-04-2020-0009","title":"The use of the Montreal Cognitive Assessment (MoCA) to assess cognitive impairment in Prader-Willi syndrome","year":2020,"lang":"en","type":"article","venue":"Advances in Mental Health and Intellectual Disabilities","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":0,"is_retracted":false,"has_abstract":true,"route_ca_aff":false,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":true,"ca_institutions":"","funders":"","keywords":"Montreal Cognitive Assessment; Normative; Psychology; Cognition; Population; Neuropsychological assessment; Cronbach's alpha; Developmental psychology; Clinical psychology; Neuropsychology; Psychometrics; Psychiatry; Medicine; Cognitive impairment","score_opus":0.042927487114125196,"score_gpt":0.33232331579522195,"score_spread":0.28939582868109676,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W3089698622","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9870186,0.0028397785,0.0033512572,0.00038623932,0.00006709616,0.00020856078,0.0007901853,0.00006861646,0.005269734],"genre_scores_gemma":[0.9949361,0.0006372626,0.0034501462,0.00007838023,0.000022434904,0.00011416791,0.00030710196,0.00000484244,0.00044962097],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9991278,0.00027510212,0.00013932405,0.000124908,0.00026705296,0.000065837834],"domain_scores_gemma":[0.9976937,0.0004932194,0.0008030975,0.00017214695,0.000626891,0.00021096691],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0017094731,0.0006195797,0.00029027375,0.002338144,0.0005165169,0.0006139416,0.000558254,0.00033922496,0.00097171584],"category_scores_gemma":[0.009330376,0.00010403729,0.00040923653,0.00081236934,0.00049472135,0.00061827985,0.00086581806,0.0006134397,0.00015004328],"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":[0.00011121896,0.000072002425,0.91863316,0.00011044842,0.00012449935,0.00035503283,0.00051076943,0.0004368457,0.0013646671,0.00037309524,0.00091717986,0.076991156],"study_design_scores_gemma":[0.000011938504,0.00024141904,0.99428326,0.00009774232,0.000047540085,0.0015386523,0.00031937868,0.0008386428,0.0009015378,0.0005306131,0.0011626799,0.000026579823],"about_ca_topic_score_codex":0.029621065,"about_ca_topic_score_gemma":0.04383476,"teacher_disagreement_score":0.029621065,"about_ca_system_score_codex":0.00077365135,"about_ca_system_score_gemma":0.0011400443,"threshold_uncertainty_score":0.058897316},"labels":[],"label_agreement":null},{"id":"W3090851569","doi":"10.1097/yct.0000000000000722","title":"Transcranial Direct Current Stimulation for Prader-Willi Syndrome","year":2020,"lang":"en","type":"article","venue":"Journal of Ect","topic":"Genetic Syndromes and Imprinting","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":"University of Toronto; Centre for Addiction and Mental Health","funders":"","keywords":"Transcranial direct-current stimulation; Craving; Food craving; Dorsolateral prefrontal cortex; Stimulation; Medicine; Prefrontal cortex; Physical medicine and rehabilitation; Population; Psychology; Neuroscience; Cognition","score_opus":0.029014499696601376,"score_gpt":0.28049495448517736,"score_spread":0.251480454788576,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W3090851569","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9973295,0.0013760892,0.0006094712,0.000050677478,0.000017574383,0.00017063439,0.000041480056,0.000011263728,0.0003933044],"genre_scores_gemma":[0.99575293,0.0015524444,0.0017017939,0.00008086015,0.000032164247,0.00026647953,0.000096432814,0.0000022644915,0.000514519],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.99991167,0.000037518967,0.000008291632,0.000015414427,0.00001462958,0.000012371756],"domain_scores_gemma":[0.99989796,0.000039896462,0.000019870411,0.000008395427,0.000006430328,0.000027394924],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00029499058,0.0003577561,0.00041535418,0.00015888584,0.00010632155,0.000091907175,0.00022398969,0.00026387407,0.001945791],"category_scores_gemma":[0.0002532551,0.000052558116,0.0001788483,0.00008529573,0.00033008758,0.00010749533,0.00016186883,0.00041654432,0.00015852098],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.06670956,0.014018825,0.02518322,0.001767372,0.0003920316,0.0035329885,0.00032862238,0.0007847491,0.58252776,0.0006670899,0.00060711714,0.30348077],"study_design_scores_gemma":[0.026225204,0.637146,0.20729354,0.00020207826,0.00053506385,0.01715102,0.00036048438,0.0026465983,0.09978219,0.00044893645,0.008154639,0.000054273754],"about_ca_topic_score_codex":0.0003344166,"about_ca_topic_score_gemma":0.0007199898,"teacher_disagreement_score":0.001945791,"about_ca_system_score_codex":0.00011805106,"about_ca_system_score_gemma":0.0002570611,"threshold_uncertainty_score":0.006509304},"labels":[],"label_agreement":null},{"id":"W3093643846","doi":"10.1002/aur.2418","title":"<scp>CIM6P</scp>/<scp>IGF</scp>‐2 Receptor Ligands Reverse Deficits in Angelman Syndrome Model Mice","year":2020,"lang":"en","type":"article","venue":"Autism Research","topic":"Genetic Syndromes and Imprinting","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":"University of Guelph","funders":"National Institute on Aging; National Institute of Mental Health; Foundation for Angelman Syndrome Therapeutics","keywords":"UBE3A; Angelman syndrome; Insulin-like growth factor 2 receptor; Neuroscience; Neurodevelopmental disorder; Psychology; Ataxia; Receptor; Insulin-like growth factor 1 receptor; Endocrinology; Internal medicine; Medicine; Autism; Growth factor; Chemistry; Developmental psychology; Biochemistry","score_opus":0.04950761889439175,"score_gpt":0.30504289158893755,"score_spread":0.2555352726945458,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W3093643846","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9776133,0.0047240164,0.0051668747,0.00085488526,0.0002452154,0.000113010494,0.0035139339,0.0010147073,0.006754278],"genre_scores_gemma":[0.96973664,0.0035219635,0.006402664,0.00033673042,0.00006473769,0.00016113279,0.0035013105,0.00012870638,0.016146153],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.999905,0.000013677032,0.00000879207,0.000015909605,0.0000313669,0.00002523227],"domain_scores_gemma":[0.99991393,0.00000870884,0.00002988736,0.000008292797,0.000007497508,0.00003158707],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00012868179,0.0005757819,0.0003206631,0.00038642538,0.00011962583,0.00021885554,0.0003327679,0.00047794994,0.003793978],"category_scores_gemma":[0.00006298313,0.00014982326,0.00032767674,0.00010783598,0.0002763636,0.00017612251,0.00011937207,0.0010506595,0.00096410385],"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":[0.00034753012,0.000081191756,0.00015040142,0.00006505934,0.000014407965,0.00009651621,0.000008129918,0.00014474284,0.9960259,0.00019592112,0.00041033514,0.0024599126],"study_design_scores_gemma":[0.00017733265,0.0011523591,0.003036926,0.000021076343,0.000045180233,0.00040185588,0.000031017673,0.0012183472,0.98443776,0.00009917982,0.009368135,0.000010747509],"about_ca_topic_score_codex":0.0011220168,"about_ca_topic_score_gemma":0.0020085901,"teacher_disagreement_score":0.003793978,"about_ca_system_score_codex":0.00031842853,"about_ca_system_score_gemma":0.0003280975,"threshold_uncertainty_score":0.012692153},"labels":[],"label_agreement":null},{"id":"W3108052922","doi":"10.3389/fcell.2020.583801","title":"mTORC1 Transcriptional Regulation of Ribosome Subunits, Protein Synthesis, and Molecular Transport in Primary Human Trophoblast Cells","year":2020,"lang":"en","type":"article","venue":"Frontiers in Cell and Developmental Biology","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":34,"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":"Eunice Kennedy Shriver National Institute of Child Health and Human Development; National Institute of Diabetes and Digestive and Kidney Diseases; National Institutes of Health","keywords":"mTORC1; Biology; Cell biology; Ribosome biogenesis; Ribosomal protein; Ribosomal protein s6; Gene; TOR signaling; PI3K/AKT/mTOR pathway; P70-S6 Kinase 1; Signal transduction; Ribosome; Genetics; RNA","score_opus":0.006403641789978965,"score_gpt":0.18128965346610146,"score_spread":0.1748860116761225,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W3108052922","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9833714,0.00452175,0.004832943,0.00015925487,0.000044809505,0.000032046948,0.0045987866,0.00015314647,0.0022859129],"genre_scores_gemma":[0.9863933,0.0024506222,0.0036304283,0.000079713966,0.000020586556,0.00008257334,0.0044859853,0.00003351786,0.0028232392],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.999851,0.000018462037,0.000013260981,0.00004951669,0.000041797848,0.000025948293],"domain_scores_gemma":[0.9999521,0.000013731235,0.000011275569,0.0000048112533,0.000008363795,0.000009690677],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.000099386634,0.00020638529,0.00027903475,0.0003325301,0.00021225095,0.00024925722,0.00007540933,0.00011188233,0.0010349853],"category_scores_gemma":[0.00013739013,0.00013616715,0.00021437899,0.00035659276,0.00018752884,0.00007740926,0.00017116027,0.00021809852,0.00034208383],"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":[0.00019517832,0.000007223757,0.0012078686,0.000047601206,0.0000081410435,0.00010345725,0.000033084212,0.00008004978,0.99612373,0.00009763184,0.00015363043,0.0019423328],"study_design_scores_gemma":[0.000018428389,0.0001526744,0.06391715,0.000009434461,0.000046809677,0.0007665312,0.00007117666,0.0015532039,0.9275065,0.00010645804,0.005842383,0.000009288655],"about_ca_topic_score_codex":0.0015834679,"about_ca_topic_score_gemma":0.0016579507,"teacher_disagreement_score":0.0015834679,"about_ca_system_score_codex":0.00027874176,"about_ca_system_score_gemma":0.00028953576,"threshold_uncertainty_score":0.0034623146},"labels":[],"label_agreement":null},{"id":"W3113794034","doi":"10.1097/brs.0000000000003879","title":"The Association of Scoliosis and NSD1 Gene Deletion in Sotos Syndrome Patients","year":2020,"lang":"en","type":"article","venue":"Spine","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","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":"Hospital for Sick Children","funders":"","keywords":"Sotos syndrome; Scoliosis; Medicine; Haploinsufficiency; Pediatrics; Genetics; Phenotype; Gene; Biology; Surgery","score_opus":0.005035252808327655,"score_gpt":0.20247464127393064,"score_spread":0.197439388465603,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W3113794034","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99963033,0.000082828075,0.000053267253,0.000004900309,0.0000014549233,0.0000079045085,0.000056428442,0.0000014802202,0.00016139423],"genre_scores_gemma":[0.9996395,0.000046801688,0.00006285543,0.00001196452,0.000005587767,0.00001887813,0.0001589526,0.0000010450603,0.000054500175],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99947864,0.0001186876,0.00006317835,0.00018112098,0.00008223673,0.00007617327],"domain_scores_gemma":[0.99894387,0.00028123416,0.00035580105,0.00008338737,0.00012299749,0.00021265767],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0004581528,0.00032947733,0.00038872458,0.0010412977,0.0004354448,0.0003119846,0.00022236885,0.00053572713,0.0025873515],"category_scores_gemma":[0.001408364,0.00026228733,0.00030208362,0.00072815135,0.0003598567,0.00034409508,0.0003715871,0.00024076909,0.00035790977],"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":[0.00018236264,0.000036450892,0.9972486,0.0000106826155,0.000025376328,0.0008770248,0.00008977534,0.000023605182,0.0005746975,0.00001696277,0.00003146441,0.0008829745],"study_design_scores_gemma":[0.00005060203,0.0010386433,0.9838665,0.000010886238,0.00006198743,0.013512587,0.00046457426,0.00018133577,0.00029323032,0.00003209646,0.00047693736,0.000010752301],"about_ca_topic_score_codex":0.0009002999,"about_ca_topic_score_gemma":0.0008105001,"teacher_disagreement_score":0.0025873515,"about_ca_system_score_codex":0.00018767695,"about_ca_system_score_gemma":0.00026374226,"threshold_uncertainty_score":0.008655548},"labels":[],"label_agreement":null},{"id":"W3113925640","doi":"","title":"Evidence for a cilia component in Axenfeld-Rieger Syndrome","year":2019,"lang":"en","type":"article","venue":"Investigative Ophthalmology & Visual Science","topic":"Genetic Syndromes and Imprinting","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":"University of Alberta","funders":"","keywords":"Component (thermodynamics); Cilium; Biology; Physics; Cell biology","score_opus":0.06236117749293582,"score_gpt":0.3516625539148661,"score_spread":0.2893013764219303,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W3113925640","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9890687,0.0033346813,0.0014921414,0.0004034672,0.000054275046,0.000018777162,0.00048046018,0.00013583191,0.005011679],"genre_scores_gemma":[0.99783427,0.000597526,0.000839428,0.00006300616,0.000027531107,0.000008435198,0.00017680429,0.000014512745,0.0004386193],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9995536,0.000059388763,0.00008315198,0.000079383084,0.0001484615,0.00007599576],"domain_scores_gemma":[0.9984048,0.00094233133,0.00024836962,0.00013946803,0.00012997283,0.00013500299],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00045467055,0.00091131905,0.0005977665,0.003987484,0.0006662716,0.0006939797,0.0012442613,0.0019800267,0.005444762],"category_scores_gemma":[0.0024410717,0.00045801175,0.00055629486,0.0013845407,0.0014240891,0.00045974768,0.00070028985,0.00053472724,0.00069404877],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.003112946,0.00018424493,0.12992008,0.0005435672,0.0005686681,0.27602863,0.0010735685,0.0013249681,0.5642686,0.0071631735,0.0008819336,0.014929613],"study_design_scores_gemma":[0.0003973349,0.0006941235,0.3705415,0.0001554464,0.0016297473,0.36088753,0.0011420802,0.004724036,0.24353756,0.0046191458,0.011574974,0.00009652541],"about_ca_topic_score_codex":0.0026666983,"about_ca_topic_score_gemma":0.0012184352,"teacher_disagreement_score":0.005444762,"about_ca_system_score_codex":0.00030785459,"about_ca_system_score_gemma":0.00045749557,"threshold_uncertainty_score":0.018214583},"labels":[],"label_agreement":null},{"id":"W3115333912","doi":"10.6215/fjpt.2018.75.p60","title":"【論文摘要】以家庭為中心概念執行普瑞德威利症候群嬰兒早期介入：個案報告","year":2018,"lang":"zh","type":"article","venue":"物理治療","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":0,"is_retracted":false,"has_abstract":true,"route_ca_aff":false,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":true,"ca_institutions":"","funders":"","keywords":"Computer science","score_opus":0.01052740576619488,"score_gpt":0.248949996840862,"score_spread":0.23842259107466712,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W3115333912","genre_codex":"other","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":[0.10508273,0.0061952528,0.017065208,0.059630442,0.00090195774,0.00019561374,0.00039949216,0.00014899203,0.8103803],"genre_scores_gemma":[0.9351858,0.0044226553,0.010791637,0.0031856953,0.00023324063,0.00022891922,0.0001475542,0.000039892762,0.045764748],"study_design_codex":"theoretical_or_conceptual","study_design_gemma":"case_report","domain_scores_codex":[0.99620616,0.0015289616,0.00019046762,0.0006372362,0.0010349714,0.00040218935],"domain_scores_gemma":[0.99499726,0.0022921364,0.0004967786,0.00019731083,0.0014229037,0.0005937015],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0053095026,0.00051795505,0.00050943077,0.0031620297,0.008434381,0.009544382,0.0011470567,0.001682531,0.009436272],"category_scores_gemma":[0.010679596,0.00039089535,0.00055580115,0.0040454734,0.013381199,0.012136521,0.0029866775,0.0024572462,0.0011993023],"study_design_candidate":"case_report","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.000009359758,0.000024993606,0.0022547718,0.00007216844,0.000015005054,0.00008778222,0.015929908,0.0005254804,0.00007974838,0.95966494,0.0066502574,0.014685601],"study_design_scores_gemma":[0.000020618329,0.000025112122,0.0034349125,0.00033038677,0.00004155554,0.00012428267,0.05775621,0.0009985256,0.00043767656,0.79614764,0.14063783,0.000045183937],"about_ca_topic_score_codex":0.037887063,"about_ca_topic_score_gemma":0.030413833,"teacher_disagreement_score":0.037887063,"about_ca_system_score_codex":0.011342405,"about_ca_system_score_gemma":0.02017261,"threshold_uncertainty_score":0.0822953},"labels":[],"label_agreement":null},{"id":"W3124329809","doi":"10.3390/genes12020172","title":"Paternal Uniparental Disomy of the Entire Chromosome 20 in a Child with Beckwith-Wiedemann Syndrome","year":2021,"lang":"en","type":"article","venue":"Genes","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":7,"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; Hospital for Sick Children","funders":"Canadian Institutes of Health Research","keywords":"Uniparental disomy; Genomic imprinting; Genetics; Biology; Beckwith–Wiedemann syndrome; Imprinting (psychology); DNA methylation; Epigenetics; Locus (genetics); SNP array; Differentially methylated regions; Chromosome; Single-nucleotide polymorphism; Karyotype; Gene; Genotype","score_opus":0.005121358447455173,"score_gpt":0.19804596692051832,"score_spread":0.19292460847306314,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W3124329809","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99556386,0.0010097252,0.00092805014,0.00052349636,0.0000765156,0.000029011815,0.00018425782,0.00008990746,0.0015952163],"genre_scores_gemma":[0.99802834,0.00055933715,0.00070504163,0.0001982196,0.00006859308,0.000009112694,0.00008903827,0.0000137495,0.00032845425],"study_design_codex":"case_report","study_design_gemma":"case_report","domain_scores_codex":[0.99961275,0.000048769474,0.0000399461,0.000118416676,0.00009290519,0.00008717478],"domain_scores_gemma":[0.9995617,0.0001055546,0.00009999419,0.000016360305,0.000022568116,0.00019381534],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00020231222,0.0012556285,0.0006019567,0.001743748,0.0010585644,0.0005373706,0.0005572397,0.0013271789,0.0015223338],"category_scores_gemma":[0.0011713677,0.0006355286,0.0003709863,0.0010116305,0.001022772,0.00043174447,0.0011411553,0.0010452509,0.00025995212],"study_design_candidate":"case_report","study_design_consensus":"case_report","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00012776011,0.00006799604,0.051773246,0.000046772722,0.000035673565,0.9328395,0.0006424666,0.00011321661,0.008783949,0.00033113052,0.00047165697,0.004766595],"study_design_scores_gemma":[0.00001826477,0.00016997974,0.05036835,0.000020507683,0.000042151896,0.9468996,0.00019893315,0.00018263837,0.0012231838,0.00012881355,0.00072914094,0.000018420174],"about_ca_topic_score_codex":0.0029440245,"about_ca_topic_score_gemma":0.0034550484,"teacher_disagreement_score":0.0029440245,"about_ca_system_score_codex":0.00044519722,"about_ca_system_score_gemma":0.00060494343,"threshold_uncertainty_score":0.005853772},"labels":[],"label_agreement":null},{"id":"W3129589084","doi":"10.1093/cdn/nzab016","title":"Effect of High-Protein Diet on Postprandial Energy Expenditure in Children with Prader-Willi Syndrome: A Pilot and Feasibility Study","year":2021,"lang":"en","type":"article","venue":"Current Developments in Nutrition","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":2,"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":"Saudi Arabian Cultural Bureau; Saudi Arabian Cultural Mission; Women and Children's Health Research Institute; Children's Health Research Institute","keywords":"Postprandial; Energy expenditure; Medicine; Internal medicine; Endocrinology; Pediatrics; Gerontology; Insulin","score_opus":0.012751954866017457,"score_gpt":0.27128064610643127,"score_spread":0.25852869124041383,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W3129589084","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99972945,0.000029704379,0.00010672207,0.0000051514703,0.0000016117255,0.00003648231,0.000023850185,0.0000022346203,0.000064709406],"genre_scores_gemma":[0.9989048,0.000059653747,0.0007878002,0.000016095066,0.000005590022,0.0000889079,0.00006132771,0.0000018981004,0.00007384873],"study_design_codex":"observational","study_design_gemma":"nonrandomized_trial","domain_scores_codex":[0.9993358,0.00040930303,0.000036771708,0.000080681755,0.00008094781,0.00005644292],"domain_scores_gemma":[0.9989845,0.0004536215,0.0001818754,0.00009191917,0.00007938837,0.00020858979],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0013149813,0.0005411336,0.00043344035,0.00025448858,0.0003157378,0.00025022254,0.0002267163,0.000336449,0.0006955864],"category_scores_gemma":[0.0018095063,0.00022940234,0.00041346348,0.00021865862,0.0004379882,0.00036473607,0.00039626835,0.00047684668,0.00012995584],"study_design_candidate":"nonrandomized_trial","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.051951315,0.018913327,0.8550423,0.00023023936,0.0003113959,0.0011633425,0.0010625088,0.00049714604,0.04159624,0.000087025895,0.00015594189,0.028989144],"study_design_scores_gemma":[0.0011569462,0.12391399,0.8694253,0.0000089497835,0.00012771899,0.00073846884,0.0004811123,0.0005440469,0.0032506997,0.000024064218,0.00030922136,0.000019518133],"about_ca_topic_score_codex":0.0015038906,"about_ca_topic_score_gemma":0.0016808226,"teacher_disagreement_score":0.0015038906,"about_ca_system_score_codex":0.00020378048,"about_ca_system_score_gemma":0.0003361747,"threshold_uncertainty_score":0.006954372},"labels":[],"label_agreement":null},{"id":"W3133907890","doi":"10.1073/pnas.2015505118","title":"<i>Dlk1</i> dosage regulates hippocampal neurogenesis and cognition","year":2021,"lang":"en","type":"article","venue":"Proceedings of the National Academy of Sciences","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":37,"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":"Medical Research Council; Banco Bilbao Vizcaya Argentaria; Generalitat Valenciana; Ministerio de Economía y Competitividad; European Commission; Ministerio de Ciencia e Innovación; Wellcome Trust; Fundación BBVA","keywords":"Neurogenesis; Subgranular zone; Subventricular zone; Dentate gyrus; Hippocampal formation; Hippocampus; Neuroscience; Lateral ventricles; Biology; Cognition; Neural stem cell; Psychology; Stem cell; Cell biology","score_opus":0.022141435783407437,"score_gpt":0.2672747866014067,"score_spread":0.24513335081799925,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W3133907890","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9935235,0.0015563997,0.0009738,0.00027544785,0.000026749956,0.0000072012326,0.0009166432,0.00012321866,0.0025969958],"genre_scores_gemma":[0.99496436,0.0005671322,0.00063974963,0.000083718165,0.00000800456,0.000011462144,0.00040863184,0.00004410161,0.0032729073],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99989665,0.000009663323,0.000009208504,0.000031378033,0.000025206205,0.00002792178],"domain_scores_gemma":[0.9998739,0.000012814748,0.00004894494,0.000010304837,0.0000078766925,0.000046154324],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00006929561,0.00030460051,0.0002240512,0.00046238556,0.00019138496,0.0004308562,0.00023297277,0.0002576377,0.0025604446],"category_scores_gemma":[0.00010810985,0.00013672936,0.00012798634,0.00016561692,0.00038484673,0.00014977399,0.00026887783,0.0004446772,0.00046003042],"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":[0.0002393796,0.000021582784,0.0012105674,0.000022762833,0.00000897311,0.000110700086,0.0000158774,0.00012877097,0.99449027,0.00028263836,0.0001648563,0.0033035534],"study_design_scores_gemma":[0.00003757604,0.00013503562,0.044017833,0.000015303063,0.000039572933,0.00081937655,0.00008704364,0.0010795665,0.94911903,0.00028389253,0.004352091,0.000013699863],"about_ca_topic_score_codex":0.0011178507,"about_ca_topic_score_gemma":0.0022481787,"teacher_disagreement_score":0.0025604446,"about_ca_system_score_codex":0.0006370069,"about_ca_system_score_gemma":0.00015529583,"threshold_uncertainty_score":0.0085654855},"labels":[],"label_agreement":null},{"id":"W3142078217","doi":"10.4021/jem198w","title":"Pseudopseudohypoparathyroidism With a Novel Mutation in the GNAS Gene Showing Thin Bones of Extremities and Ossification of Entheses","year":2013,"lang":"en","type":"article","venue":"Journal of Endocrinology and Metabolism","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":1,"is_retracted":false,"has_abstract":true,"route_ca_aff":false,"route_ca_fund":false,"route_ca_venue":true,"route_about_ca":false,"ca_institutions":"","funders":"National Center for Global Health and Medicine","keywords":"GNAS complex locus; Medicine; Ossification; Heterotopic ossification; Osteodystrophy; Pseudohypoparathyroidism; Internal medicine; Short stature; Endocrinology; Gene; Anatomy; Parathyroid hormone; Genetics; Biology","score_opus":0.01863866593083609,"score_gpt":0.23944879154916862,"score_spread":0.22081012561833252,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W3142078217","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99532807,0.0004512131,0.0014673088,0.0004497044,0.000053801552,0.000029156647,0.00011133246,0.000051956627,0.0020573915],"genre_scores_gemma":[0.9981018,0.00022788694,0.000824192,0.000102799786,0.00006530533,0.000009647678,0.00004822225,0.000009639704,0.0006106159],"study_design_codex":"case_report","study_design_gemma":"case_report","domain_scores_codex":[0.9996848,0.000027792237,0.00004062486,0.00011269358,0.00007101615,0.000063102074],"domain_scores_gemma":[0.9994715,0.00018391367,0.00012007629,0.000029915902,0.000027218586,0.0001674315],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00015331426,0.0011830447,0.0005402443,0.001205956,0.00068734953,0.00048622387,0.00052343856,0.0016236834,0.002060796],"category_scores_gemma":[0.0010424521,0.0005345265,0.0005443448,0.0007209493,0.0010861378,0.0005846396,0.0008777221,0.0008135139,0.00035143105],"study_design_candidate":"case_report","study_design_consensus":"case_report","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0000576733,0.000024935522,0.0067092,0.000023302588,0.000013697642,0.97929126,0.000116099545,0.00006698327,0.0122366445,0.00022445139,0.000080778766,0.0011550038],"study_design_scores_gemma":[0.000021527445,0.000060861454,0.008724455,0.0000035508078,0.000017934355,0.98831826,0.000044399683,0.00022588742,0.0021776215,0.00013793769,0.0002594541,0.000008253057],"about_ca_topic_score_codex":0.0009593492,"about_ca_topic_score_gemma":0.0010379599,"teacher_disagreement_score":0.002060796,"about_ca_system_score_codex":0.0003446721,"about_ca_system_score_gemma":0.00036371834,"threshold_uncertainty_score":0.006894052},"labels":[],"label_agreement":null},{"id":"W3148518460","doi":"10.1002/epi4.12484","title":"Seizures in Sotos syndrome: Phenotyping in 49 patients","year":2021,"lang":"en","type":"article","venue":"Epilepsia Open","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":15,"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; McGill University Health Centre; Université de Sherbrooke; McGill University; Montreal Children's Hospital","funders":"Medical Research Council; National Health and Medical Research Council; McGill University; McGill University Health Centre; Citizens United for Research in Epilepsy","keywords":"Sotos syndrome; Epilepsy; Pediatrics; Medicine; Epilepsy syndromes; Seizure types; Levetiracetam; Semiology; Macrocephaly; Psychiatry","score_opus":0.011955994704059449,"score_gpt":0.2639440680920125,"score_spread":0.25198807338795304,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W3148518460","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99938893,0.00010104867,0.000074337564,0.00002155418,0.0000025770407,0.0000099717945,0.0000761,0.0000036267795,0.00032176042],"genre_scores_gemma":[0.99953353,0.00009172417,0.00009047634,0.000030488754,0.000005620367,0.000009174556,0.00015919817,0.0000021972742,0.00007765006],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99970895,0.00005335941,0.000044131917,0.00005983395,0.000072478455,0.000061242295],"domain_scores_gemma":[0.9996482,0.00008197997,0.00011840179,0.000017875589,0.000031830903,0.00010164366],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0001334685,0.00047928537,0.00026594664,0.00071843766,0.00035997867,0.0003035479,0.00014471631,0.00031918107,0.0012422932],"category_scores_gemma":[0.0011092055,0.0001922121,0.00018629112,0.0005234211,0.00032846932,0.00021830323,0.0004164123,0.00015760357,0.00022845027],"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":[0.0002414953,0.00006091626,0.9516571,0.00002765932,0.000024662042,0.03420027,0.00076298235,0.00019047128,0.0047105853,0.00010815737,0.0004558601,0.0075598606],"study_design_scores_gemma":[0.00004903443,0.00038872877,0.9024767,0.000026342832,0.000036095633,0.09329783,0.0007579757,0.00060668995,0.0008215078,0.0002052166,0.0013120685,0.000021797858],"about_ca_topic_score_codex":0.0015089479,"about_ca_topic_score_gemma":0.0013072018,"teacher_disagreement_score":0.0015089479,"about_ca_system_score_codex":0.00019321906,"about_ca_system_score_gemma":0.00015424332,"threshold_uncertainty_score":0.0041558146},"labels":[],"label_agreement":null},{"id":"W3151565048","doi":"10.14740/jem235w","title":"Erratum to: Pseudopseudohypoparathyroidism With a Novel Mutation in the GNAS Gene Showing Thin Bones of Extremities and Ossification of Entheses","year":2014,"lang":"en","type":"erratum","venue":"Journal of Endocrinology and Metabolism","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":0,"is_retracted":false,"has_abstract":true,"route_ca_aff":false,"route_ca_fund":false,"route_ca_venue":true,"route_about_ca":false,"ca_institutions":"","funders":"","keywords":"GNAS complex locus; Medicine; Exon; Ossification; Gene; Endocrinology; Internal medicine; Genetics; Anatomy; Biology","score_opus":0.01898992797138789,"score_gpt":0.25264973405704977,"score_spread":0.2336598060856619,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W3151565048","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":[0.017641747,0.012583927,0.0047681574,0.16711073,0.7857324,0.00010866199,0.0017020272,0.0007795422,0.009572826],"genre_scores_gemma":[0.26881248,0.033963468,0.03221857,0.20678829,0.19425777,0.0002881833,0.0054155374,0.0022060198,0.2560497],"study_design_codex":"not_applicable","study_design_gemma":"not_applicable","domain_scores_codex":[0.99898666,0.00012996403,0.00028658763,0.00019629054,0.0003058674,0.00009457078],"domain_scores_gemma":[0.99734867,0.0009527513,0.0002921716,0.00012752668,0.0010943054,0.00018462441],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00071331084,0.0014213062,0.001279277,0.0015487124,0.0013906724,0.0010355874,0.0018263045,0.0058196317,0.012125024],"category_scores_gemma":[0.006979285,0.000765545,0.0009981038,0.001041131,0.0011592027,0.0015207437,0.0008188082,0.004717572,0.006727356],"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":[0.00033831492,0.00009431931,0.0024734694,0.0005667784,0.00008984001,0.10976496,0.00042999984,0.00030106053,0.0019845956,0.0024810908,0.85591733,0.025558135],"study_design_scores_gemma":[0.0001706037,0.00014962799,0.007329755,0.0006763072,0.0002545355,0.20199016,0.000611389,0.0010522902,0.0038962094,0.0021189244,0.7815816,0.00016866565],"about_ca_topic_score_codex":0.0052821883,"about_ca_topic_score_gemma":0.005141262,"teacher_disagreement_score":0.012125024,"about_ca_system_score_codex":0.0016751887,"about_ca_system_score_gemma":0.0011266044,"threshold_uncertainty_score":0.040562212},"labels":[],"label_agreement":null},{"id":"W3159797256","doi":"10.1210/jendso/bvab048.1403","title":"Topline Results of the CARE-PWS Phase 3 Study: Intranasal Carbetocin Improves Hyperphagia and Anxiety and Distress Symptoms in Prader-Willi Syndrome (PWS)","year":2021,"lang":"en","type":"article","venue":"Journal of the Endocrine Society","topic":"Genetic Syndromes and Imprinting","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":"Université de Montréal; Centre Hospitalier Universitaire Sainte-Justine","funders":"","keywords":"Medicine; Placebo; Clinical endpoint; Anxiety; Internal medicine; Tolerability; Distress; Randomized controlled trial; Pediatrics; Adverse effect; Psychiatry; Clinical psychology","score_opus":0.005396942329276989,"score_gpt":0.2542645968719744,"score_spread":0.2488676545426974,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W3159797256","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.97704256,0.004912423,0.0011119115,0.0010767805,0.00039730433,0.006916214,0.004942017,0.00026737753,0.0033334242],"genre_scores_gemma":[0.97292095,0.003504057,0.0031370525,0.0023725387,0.00040535157,0.007676147,0.005241899,0.00008071814,0.0046612564],"study_design_codex":"randomized_trial","study_design_gemma":"randomized_trial","domain_scores_codex":[0.9994797,0.00025428823,0.00003323628,0.00006971705,0.00007408061,0.000088968656],"domain_scores_gemma":[0.9989907,0.0001941755,0.00023877823,0.00008349243,0.00015402735,0.00033883646],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0016984789,0.0011819393,0.0018457534,0.0003673396,0.00049887673,0.0008193136,0.0009493514,0.0017311703,0.007527049],"category_scores_gemma":[0.0015915685,0.00038462467,0.0019461699,0.00030141647,0.0007047716,0.00072992267,0.00027734472,0.002704625,0.00091709854],"study_design_candidate":"randomized_trial","study_design_consensus":"randomized_trial","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.8674448,0.03165176,0.0023199935,0.0016936641,0.0016494907,0.0001647952,0.00015409726,0.0005491875,0.029481236,0.00020413578,0.0067887357,0.057898056],"study_design_scores_gemma":[0.8134543,0.17394872,0.007989531,0.00006507391,0.00044482158,0.000084704916,0.00003356234,0.0003151667,0.0018618047,0.00008971108,0.0016919402,0.000020675938],"about_ca_topic_score_codex":0.0014899728,"about_ca_topic_score_gemma":0.0047325986,"teacher_disagreement_score":0.007527049,"about_ca_system_score_codex":0.0006826867,"about_ca_system_score_gemma":0.0013371182,"threshold_uncertainty_score":0.025180519},"labels":[],"label_agreement":null},{"id":"W3163620746","doi":"10.1093/jas/skab140","title":"Genetic potential for residual feed intake and diet fed during early- to mid-gestation influences post-natal DNA methylation of imprinted genes in muscle and liver tissues in beef cattle","year":2021,"lang":"en","type":"article","venue":"Journal of Animal Science","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":17,"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; Agriculture and Agri-Food Canada","funders":"Alberta Livestock and Meat Agency","keywords":"Biology; Residual feed intake; DNA methylation; Genomic imprinting; Beef cattle; Epigenetics; Offspring; Gestation; Methylation; Animal science; Genetics; Andrology; Endocrinology; Gene; Pregnancy; Feed conversion ratio; Gene expression; Body weight; Medicine","score_opus":0.010010109750430523,"score_gpt":0.26452106651556917,"score_spread":0.25451095676513863,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W3163620746","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9996829,0.00007312133,0.000117667565,0.000004491471,7.5262574e-7,0.0000011249127,0.000051935367,0.0000012809093,0.00006688466],"genre_scores_gemma":[0.99905413,0.00007147267,0.00023646174,0.0000110406945,0.000001268631,0.000007339504,0.00017727436,0.000002788422,0.0004381586],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.99985564,0.00002860397,0.0000070749034,0.00004987265,0.000025928923,0.000032833228],"domain_scores_gemma":[0.9998354,0.000035315115,0.000057939684,0.000010320275,0.000016180995,0.000044815293],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00014814072,0.00015820735,0.0001628095,0.00028294494,0.0001564289,0.00019768067,0.00013099394,0.00016223613,0.0006066383],"category_scores_gemma":[0.00017700774,0.00014232175,0.000121332174,0.00013785902,0.00017301114,0.000083687744,0.00012942185,0.00022122457,0.00007158088],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.001489233,0.00007385637,0.12926991,0.000022476937,0.00006156934,0.00010241314,0.00033510572,0.000079519195,0.8643328,0.000043686185,0.000022821601,0.0041665817],"study_design_scores_gemma":[0.0000050817735,0.00028032443,0.986387,0.0000024335784,0.000024140703,0.00011628818,0.00010960475,0.00015445298,0.012774098,0.000015901282,0.0001270744,0.0000036145966],"about_ca_topic_score_codex":0.004722953,"about_ca_topic_score_gemma":0.012251102,"teacher_disagreement_score":0.004722953,"about_ca_system_score_codex":0.00035016643,"about_ca_system_score_gemma":0.00014851638,"threshold_uncertainty_score":0.00939095},"labels":[],"label_agreement":null},{"id":"W3164396936","doi":"10.14218/jcth.2021.00016","title":"Identification of Expression Pattern and Clinical Significance of the Small Cajal Body-specific RNA SCARNA16 in Hepatocellular Carcinoma","year":2021,"lang":"en","type":"article","venue":"Journal of Clinical and Translational Hepatology","topic":"Genetic Syndromes and Imprinting","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":"Pancreas Centre (Canada)","funders":"National Natural Science Foundation of China","keywords":"Clinical significance; Hepatocellular carcinoma; Biomarker; Identification (biology); Messenger RNA; RNA; Small nucleolar RNA; Potency","score_opus":0.039646243047157886,"score_gpt":0.31139116357049795,"score_spread":0.2717449205233401,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W3164396936","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9993734,0.00020721025,0.00016384757,0.000016245942,0.0000025797399,0.0000025038676,0.000050500206,0.000003964886,0.00017973917],"genre_scores_gemma":[0.9995499,0.000060160386,0.0001490976,0.000006031593,0.000004519255,0.0000034442146,0.00008099527,0.0000013636333,0.00014446543],"study_design_codex":"observational","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99990416,0.000020143743,0.000012348926,0.000026253208,0.000018059402,0.000018948322],"domain_scores_gemma":[0.99947935,0.00013601902,0.00019712685,0.000035385427,0.000043690252,0.000108497916],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0002764983,0.00012189402,0.00014850647,0.0006173489,0.00013968896,0.00023679911,0.000115599774,0.00021303903,0.0012090609],"category_scores_gemma":[0.0007263269,0.00008950309,0.00010625324,0.0003365098,0.0002879674,0.0001492169,0.00015495665,0.00020861617,0.00015488532],"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":[0.0010343618,0.0000351263,0.9231445,0.00003581825,0.000033733017,0.0005820008,0.000094956034,0.000108392225,0.06866881,0.00006247552,0.00007023301,0.0061295163],"study_design_scores_gemma":[0.000020808404,0.00027046428,0.9778153,0.000006889817,0.0000443555,0.0031616332,0.00019632009,0.0008216007,0.016996378,0.00015379683,0.0005051868,0.000007257373],"about_ca_topic_score_codex":0.00024391702,"about_ca_topic_score_gemma":0.00024746964,"teacher_disagreement_score":0.0012090609,"about_ca_system_score_codex":0.00012391173,"about_ca_system_score_gemma":0.00011644425,"threshold_uncertainty_score":0.004044652},"labels":[],"label_agreement":null},{"id":"W3165895781","doi":"10.1016/j.aace.2021.06.003","title":"A Case Report of Hyperestrogenism in Prader-Willi Syndrome","year":2021,"lang":"en","type":"article","venue":"AACE Clinical Case Reports","topic":"Genetic Syndromes and Imprinting","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":"McGill University Health Centre; McGill University","funders":"","keywords":"Medicine; Hyperandrogenism; Polycystic ovary; Estrogen; Concomitant; Hormone replacement therapy (female-to-male); Estrone; Internal medicine; Endocrinology; Pediatrics; Insulin; Testosterone (patch); Insulin resistance","score_opus":0.04309169645467011,"score_gpt":0.34307316042811864,"score_spread":0.29998146397344855,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W3165895781","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.95428306,0.015538061,0.008493195,0.0050301803,0.00095262023,0.0004344155,0.00052710384,0.0004386663,0.014302592],"genre_scores_gemma":[0.9894159,0.002939138,0.003187471,0.0009007457,0.001381333,0.0000714998,0.00014221901,0.000033971683,0.0019279096],"study_design_codex":"case_report","study_design_gemma":"case_report","domain_scores_codex":[0.9990011,0.00013456469,0.00011212183,0.0003004556,0.00016706137,0.0002847906],"domain_scores_gemma":[0.99839646,0.0004494731,0.00040990007,0.00017665353,0.000111262365,0.0004561674],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00043740156,0.002187267,0.0012620209,0.004033336,0.0024176054,0.0016932912,0.0015470999,0.0056060613,0.0030283832],"category_scores_gemma":[0.0033834456,0.0013393258,0.0011940673,0.0021123528,0.0019455429,0.002275625,0.0026356142,0.0033264046,0.0010190567],"study_design_candidate":"case_report","study_design_consensus":"case_report","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.000008220032,0.000010566704,0.0020095664,0.000014188022,0.0000050612844,0.99678683,0.00006333533,0.000026513113,0.00026052044,0.00012589489,0.0001294616,0.00055990595],"study_design_scores_gemma":[0.000006583121,0.0000136283215,0.00097569765,0.0000059511553,0.000005336612,0.9983583,0.000039979383,0.00007369783,0.000096507705,0.00010792262,0.00031192965,0.000004477639],"about_ca_topic_score_codex":0.0021952677,"about_ca_topic_score_gemma":0.0022314526,"teacher_disagreement_score":0.0056060613,"about_ca_system_score_codex":0.0010858916,"about_ca_system_score_gemma":0.0010141685,"threshold_uncertainty_score":0.0101310015},"labels":[],"label_agreement":null},{"id":"W3166105596","doi":"10.1093/nar/gkab475","title":"The role of CTCF in the organization of the centromeric 11p15 imprinted domain interactome","year":2021,"lang":"en","type":"article","venue":"Nucleic Acids Research","topic":"Genetic Syndromes and Imprinting","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":"SickKids Foundation; Hospital for Sick Children; University of Toronto","funders":"National Institutes of Health; Alex's Lemonade Stand Foundation for Childhood Cancer; National Cancer Institute; Damon Runyon Cancer Research Foundation","keywords":"CTCF; Genomic imprinting; Biology; Chromatin; Imprinting (psychology); Genetics; DNA methylation; Chromosome conformation capture; Bivalent chromatin; Gene silencing; Gene; Transcription factor; Gene expression; Chromatin remodeling; Enhancer","score_opus":0.011294666021898632,"score_gpt":0.28726603073821144,"score_spread":0.2759713647163128,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W3166105596","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9910274,0.0019673805,0.0050419075,0.00013388906,0.000011770293,0.0000074753275,0.0001258999,0.0000647102,0.0016195736],"genre_scores_gemma":[0.9979722,0.00022115505,0.00094505964,0.00001640992,0.0000031432078,0.0000030918986,0.00010082702,0.0000058972028,0.0007323457],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99993086,0.000007932066,0.0000029826433,0.000018525969,0.000018547658,0.000021120106],"domain_scores_gemma":[0.9999374,0.000011238967,0.000016772463,0.000006858237,0.0000056607473,0.000022131399],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00007236418,0.00018574607,0.000106133244,0.00022217748,0.00020719485,0.0003147895,0.00021770483,0.0002306153,0.00053559215],"category_scores_gemma":[0.00016188226,0.0001253906,0.00007399145,0.00011603325,0.00023439873,0.00015313002,0.00023224133,0.0001589275,0.00016496962],"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":[0.00008954903,0.000007419073,0.005463978,0.000027286802,0.0000075581393,0.0003917467,0.000052039377,0.00039815457,0.9876094,0.00091568957,0.000069463924,0.004967716],"study_design_scores_gemma":[0.00003611151,0.00014462537,0.17187925,0.000022001886,0.000032649306,0.0026668687,0.00012721425,0.009916564,0.8067738,0.0012638683,0.0071178246,0.000019295578],"about_ca_topic_score_codex":0.0028693571,"about_ca_topic_score_gemma":0.005820277,"teacher_disagreement_score":0.0028693571,"about_ca_system_score_codex":0.00041788025,"about_ca_system_score_gemma":0.00022858163,"threshold_uncertainty_score":0.0057053566},"labels":[],"label_agreement":null},{"id":"W3169291890","doi":"10.1080/08880018.2021.1933281","title":"Allogeneic hematopoietic stem cell transplantation in an adolescent with Prader-Willi syndrome – unique considerations","year":2021,"lang":"en","type":"letter","venue":"Pediatric Hematology and Oncology","topic":"Genetic Syndromes and Imprinting","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":"Western University; SickKids Foundation; Hospital for Sick Children; London Health Sciences Centre; University of Toronto","funders":"","keywords":"Medicine; Hematopoietic stem cell transplantation; Stem cell; Transplantation; Haematopoiesis; Oncology; Immunology; Cancer research; Internal medicine; Genetics; Biology","score_opus":0.01613634671782262,"score_gpt":0.24855339131535653,"score_spread":0.2324170445975339,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W3169291890","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.5477339,0.017026732,0.009255009,0.35346958,0.018577011,0.00042642158,0.00046179202,0.00038060165,0.05266888],"genre_scores_gemma":[0.91569793,0.0065497225,0.0035386654,0.048738796,0.018452797,0.000091052774,0.00018812942,0.00007768529,0.0066651604],"study_design_codex":"case_report","study_design_gemma":"case_report","domain_scores_codex":[0.9995546,0.00010376072,0.000046937967,0.00008570115,0.00009258854,0.00011644968],"domain_scores_gemma":[0.99885464,0.0004808809,0.000109073226,0.000046281508,0.00007625818,0.0004329724],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00051002763,0.00060389726,0.00068490725,0.0007738733,0.0013600353,0.00078367844,0.00089729234,0.0057707536,0.0014903005],"category_scores_gemma":[0.00266717,0.00030060316,0.0007426256,0.00047149943,0.00091154914,0.00086802815,0.00061364705,0.0046932395,0.00048464185],"study_design_candidate":"case_report","study_design_consensus":"case_report","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00004344428,0.00008513769,0.0050930358,0.000024856474,0.000012539642,0.9811652,0.00009475666,0.00023807216,0.0005443464,0.0015320276,0.0070139696,0.0041527236],"study_design_scores_gemma":[0.000037045866,0.00013304265,0.004059305,0.00005647058,0.00001662152,0.9849924,0.00015930667,0.0011129659,0.00040255516,0.0020607589,0.0069542597,0.000015365065],"about_ca_topic_score_codex":0.0014780345,"about_ca_topic_score_gemma":0.0035181523,"teacher_disagreement_score":0.0057707536,"about_ca_system_score_codex":0.0013324382,"about_ca_system_score_gemma":0.00096715416,"threshold_uncertainty_score":0.009667516},"labels":[],"label_agreement":null},{"id":"W3185059072","doi":"10.1038/s41598-021-93885-3","title":"Human placental piwi-interacting RNA transcriptome is characterized by expression from the DLK1-DIO3 imprinted region","year":2021,"lang":"en","type":"article","venue":"Scientific Reports","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":13,"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; Capital District Health Authority; BC Cancer Agency; Izaak Walton Killam Health Centre; BC Children's Hospital; Dalhousie University","funders":"Eunice Kennedy Shriver National Institute of Child Health and Human Development; Canadian Institutes of Health Research; National Institutes of Health","keywords":"Genomic imprinting; Transcriptome; Piwi-interacting RNA; RNA; Biology; Computational biology; Gene expression; Genetics; Gene; DNA methylation; RNA interference","score_opus":0.013299611721513357,"score_gpt":0.24977501692902992,"score_spread":0.23647540520751656,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W3185059072","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9883208,0.001889036,0.004254733,0.00010543961,0.0000097891425,0.00001600693,0.0023281954,0.00012678483,0.0029491526],"genre_scores_gemma":[0.9930934,0.0008805655,0.001992831,0.000053101066,0.0000055327987,0.000013081424,0.0020952497,0.000031186308,0.0018349269],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.99992657,0.000005159572,0.0000040904415,0.000029499895,0.000021287347,0.0000134136535],"domain_scores_gemma":[0.999899,0.000018442528,0.00003988992,0.000010878726,0.000008331437,0.000023360166],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.000051044437,0.00012837232,0.0001455987,0.00038455374,0.00014712225,0.00025764873,0.000078175784,0.00010982912,0.0021327345],"category_scores_gemma":[0.00018977023,0.0001098355,0.000114375565,0.00038466608,0.00018182749,0.00007835491,0.00019849549,0.0001657133,0.00055990304],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0001993081,0.0000055304786,0.009774311,0.000053788324,0.000011815322,0.00045341701,0.00006773464,0.000037510574,0.98232424,0.00012426697,0.00010166894,0.006846331],"study_design_scores_gemma":[0.00002636714,0.00012937385,0.54019177,0.000021291555,0.000058640602,0.010084573,0.00030413468,0.0009482409,0.4339931,0.0005905802,0.013633541,0.000018446544],"about_ca_topic_score_codex":0.00068548904,"about_ca_topic_score_gemma":0.00080026087,"teacher_disagreement_score":0.0021327345,"about_ca_system_score_codex":0.00015349417,"about_ca_system_score_gemma":0.00014718469,"threshold_uncertainty_score":0.0071347356},"labels":[],"label_agreement":null},{"id":"W3186869997","doi":"10.1101/2021.07.17.452734","title":"Genome-Wide Detection of Imprinted Differentially Methylated Regions Using Nanopore Sequencing","year":2021,"lang":"en","type":"preprint","venue":"bioRxiv (Cold Spring Harbor Laboratory)","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":4,"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; University of British Columbia","funders":"University of British Columbia; Canada Research Chairs","keywords":"Genomic imprinting; Imprinting (psychology); Differentially methylated regions; Biology; DNA methylation; Nanopore sequencing; Genetics; Methylated DNA immunoprecipitation; CpG site; Genome; Computational biology; Epigenetics; Germline; Methylation; Gene; Gene expression","score_opus":0.016228537565887033,"score_gpt":0.22196470451478623,"score_spread":0.20573616694889918,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W3186869997","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9201434,0.0010437976,0.07025296,0.00018528187,0.000040919753,0.000035451074,0.0055300575,0.000681494,0.0020865968],"genre_scores_gemma":[0.9196911,0.00041655052,0.072748505,0.00018144578,0.000019141396,0.00005359447,0.0047740745,0.000091474176,0.0020240399],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99974376,0.000034214907,0.000010243751,0.00011722948,0.00007109583,0.000023356984],"domain_scores_gemma":[0.99974054,0.00010818351,0.000055482473,0.000042897413,0.000027789625,0.000025077958],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00028191792,0.00018024407,0.0002047424,0.00042710593,0.00013426629,0.00028679447,0.00022872184,0.00040790878,0.0008317136],"category_scores_gemma":[0.00043253665,0.0001359431,0.00018203254,0.00025480444,0.00019293244,0.00014394821,0.00036841276,0.00036223352,0.0003124889],"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":[0.00006629035,0.000011643081,0.0046095964,0.000029655701,0.000030579336,0.00004422135,0.000028869881,0.00046708967,0.9887583,0.00019632828,0.00014897856,0.005608493],"study_design_scores_gemma":[0.000012271748,0.000117875934,0.057461683,0.000010936121,0.000054518456,0.00048099912,0.000054918284,0.010974841,0.92360395,0.00087206863,0.0063360273,0.000019951962],"about_ca_topic_score_codex":0.0006284203,"about_ca_topic_score_gemma":0.001425222,"teacher_disagreement_score":0.0008317136,"about_ca_system_score_codex":0.0001701295,"about_ca_system_score_gemma":0.00009268714,"threshold_uncertainty_score":0.0027824044},"labels":[],"label_agreement":null},{"id":"W3191261968","doi":"10.1017/cjn.2019.150","title":"P.050 Epilepsy phenotypes in patients with Sotos syndrome","year":2019,"lang":"en","type":"article","venue":"Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques","topic":"Genetic Syndromes and Imprinting","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":true,"route_about_ca":false,"ca_institutions":"Saskatoon Medical Imaging; Sherbrooke O.E.M (Canada)","funders":"","keywords":"Sotos syndrome; Epilepsy; Macrocephaly; Medicine; Pediatrics; Levetiracetam; Epilepsy syndromes; Lamotrigine; Psychiatry","score_opus":0.009925297653657796,"score_gpt":0.21445863963426312,"score_spread":0.20453334198060533,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W3191261968","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99569714,0.00023550676,0.00013987221,0.00015426804,0.000019059691,0.0000140749535,0.00033739983,0.000011097177,0.0033915092],"genre_scores_gemma":[0.9992411,0.00007593339,0.00013589404,0.000053542666,0.0000224893,0.000009633054,0.00027241226,0.0000039239117,0.00018496416],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9998523,0.000020499232,0.000022300272,0.000036035202,0.000033839642,0.000034962304],"domain_scores_gemma":[0.9996126,0.000093256,0.0001464496,0.000015708563,0.000047994465,0.00008400563],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00013953239,0.00037171683,0.00016450639,0.00055240205,0.00034729496,0.0003143732,0.00016436465,0.00032441792,0.0065374435],"category_scores_gemma":[0.0009044774,0.0000822491,0.00016495657,0.0005096321,0.00026242316,0.00025124234,0.00031658477,0.00022667545,0.00060309086],"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":[0.0005218207,0.000066708344,0.96394354,0.000048480702,0.00003401788,0.017446171,0.00020310341,0.0001525713,0.0033643518,0.00031674074,0.0016172869,0.012285256],"study_design_scores_gemma":[0.00007427562,0.00043410403,0.88786405,0.000060485592,0.000052663625,0.10491722,0.00061529747,0.000663617,0.0008579868,0.0009448959,0.0035003803,0.0000149853895],"about_ca_topic_score_codex":0.00063940196,"about_ca_topic_score_gemma":0.0005326721,"teacher_disagreement_score":0.0065374435,"about_ca_system_score_codex":0.00014512603,"about_ca_system_score_gemma":0.00018127977,"threshold_uncertainty_score":0.021869898},"labels":[],"label_agreement":null},{"id":"W3192140173","doi":"10.1530/ec-21-0277","title":"Hypogonadism in Prader–Willi syndrome from birth to adulthood: a 28-year experience in a single centre","year":2021,"lang":"en","type":"article","venue":"Endocrine Connections","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":10,"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":"Hospital for Sick Children","keywords":"Medicine; Pediatrics; Early adulthood; Young adult; Obstetrics; Gerontology","score_opus":0.015467305862803928,"score_gpt":0.25314786956654034,"score_spread":0.2376805637037364,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W3192140173","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99951184,0.0001585567,0.00004026167,0.000033188,0.0000043915265,0.000007162755,0.000022711212,0.000004124081,0.00021771752],"genre_scores_gemma":[0.99917644,0.00030149097,0.00009576526,0.000036590038,0.0000116826395,0.0000069256703,0.00006591234,0.0000035333046,0.00030167846],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9995359,0.00008680184,0.000041461317,0.00008282681,0.00009979337,0.0001531094],"domain_scores_gemma":[0.99907196,0.0001027055,0.00024221306,0.00006298567,0.00007916917,0.00044087923],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0003979833,0.00049500837,0.00032247955,0.00048835424,0.0009866665,0.00047511735,0.0003425151,0.00040051847,0.0015039121],"category_scores_gemma":[0.0013997523,0.00030965664,0.00031279618,0.0005068398,0.00053568836,0.00041652608,0.00081709574,0.00050516106,0.00046576062],"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":[0.00012588868,0.0003412547,0.95674956,0.000028953347,0.000028458346,0.02086765,0.0034454921,0.0000795784,0.0011613569,0.000042138563,0.00036865173,0.016761044],"study_design_scores_gemma":[0.000039322247,0.0025502115,0.92473036,0.00003758276,0.00003070693,0.06570962,0.0046485476,0.0002399334,0.00044755492,0.00005129914,0.0014840983,0.00003074526],"about_ca_topic_score_codex":0.007881813,"about_ca_topic_score_gemma":0.011176977,"teacher_disagreement_score":0.007881813,"about_ca_system_score_codex":0.0006693648,"about_ca_system_score_gemma":0.00086304394,"threshold_uncertainty_score":0.015671909},"labels":[],"label_agreement":null},{"id":"W3192601169","doi":"10.1002/epi4.12528","title":"Response: Sotos Syndrome and the added value of genetic workup in epilepsy surgery","year":2021,"lang":"en","type":"letter","venue":"Epilepsia Open","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":0,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":true,"ca_institutions":"McGill University; McGill University Health Centre; Montreal Children's Hospital","funders":"Savoy Foundation; LivaNova; Biogen","keywords":"Sotos syndrome; Epilepsy; Levetiracetam; Medicine; Pediatrics; Malignancy; Epilepsy surgery; Epileptogenesis; Epilepsy syndromes; Surgery; Pathology; Psychiatry","score_opus":0.01718373920330835,"score_gpt":0.2508722893739756,"score_spread":0.23368855017066725,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W3192601169","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":[0.00067687564,0.0014729163,0.0001845352,0.9518611,0.04380586,0.000050633913,0.00016365167,0.0001234601,0.0016609705],"genre_scores_gemma":[0.00567124,0.0013834992,0.00037138353,0.92023265,0.0679372,0.000082611914,0.00010061605,0.000055891247,0.004164889],"study_design_codex":"not_applicable","study_design_gemma":"case_report","domain_scores_codex":[0.9979892,0.0005264053,0.0003168277,0.00031812445,0.0005303513,0.00031915915],"domain_scores_gemma":[0.99187005,0.003317681,0.0006225551,0.00028323513,0.0025208408,0.00138567],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.002302498,0.0011924782,0.0016643078,0.000980721,0.0016923695,0.0019278417,0.003088247,0.030250333,0.008522529],"category_scores_gemma":[0.026283106,0.00063427055,0.0016806129,0.000518101,0.0018309184,0.0033228921,0.0014854989,0.03324714,0.007118372],"study_design_candidate":"case_report","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00015485546,0.000046989462,0.0010513272,0.0001244771,0.000031319883,0.0042435327,0.00010522957,0.00012328116,0.0002134903,0.000709363,0.9861752,0.007020947],"study_design_scores_gemma":[0.00042115286,0.00032125076,0.005083601,0.0012363818,0.00010398766,0.01922941,0.00084179617,0.000994493,0.0008737982,0.0066783624,0.96393627,0.0002794489],"about_ca_topic_score_codex":0.0021334288,"about_ca_topic_score_gemma":0.0024177488,"teacher_disagreement_score":0.030250333,"about_ca_system_score_codex":0.0026033649,"about_ca_system_score_gemma":0.0016621772,"threshold_uncertainty_score":0.02851075},"labels":[],"label_agreement":null},{"id":"W3196779067","doi":"10.1523/jneurosci.0925-21.2021","title":"Excessive Laughter-like Vocalizations, Microcephaly, and Translational Outcomes in the<i>Ube3a</i>Deletion Rat Model of Angelman Syndrome","year":2021,"lang":"en","type":"article","venue":"Journal of Neuroscience","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":22,"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; University of Toronto","funders":"Canadian Institutes of Health Research; National Institute of Mental Health; Deutsche Forschungsgemeinschaft; Foundation for Angelman Syndrome Therapeutics; Ontario Brain Institute","keywords":"Laughter; Angelman syndrome; UBE3A; Neuroscience; Psychology; Neurodevelopmental disorder; Intellectual disability; Microcephaly; Disease; Phenotype; Fragile X syndrome; Developmental psychology; Medicine; Autism; Biology; Psychiatry; Genetics; Pathology","score_opus":0.018091002529620027,"score_gpt":0.2606791225541923,"score_spread":0.24258812002457225,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W3196779067","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9884242,0.0007152435,0.0057787974,0.00054984784,0.00015300179,0.00015271854,0.0018937874,0.00042443466,0.0019078617],"genre_scores_gemma":[0.979625,0.0013421378,0.008273633,0.0002523272,0.000033550037,0.00041010647,0.0017115137,0.00018865285,0.008163011],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99925977,0.00010704634,0.0000917574,0.0001467135,0.00023467837,0.0001600575],"domain_scores_gemma":[0.9989755,0.00009298437,0.0003775953,0.00009377347,0.000112402144,0.00034767253],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00073026394,0.0012870057,0.0005736563,0.0017329092,0.00053333584,0.00066243793,0.0005755973,0.0010132703,0.002369918],"category_scores_gemma":[0.0004403405,0.0003767135,0.0008760293,0.0003131011,0.0014141572,0.0005959609,0.00055068824,0.002339447,0.0006467063],"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":[0.00047045952,0.0003333014,0.00076537364,0.00006708304,0.0000215317,0.00040952655,0.000090327616,0.0002275065,0.99493057,0.00034370122,0.00020522202,0.002135328],"study_design_scores_gemma":[0.0001246572,0.0053563393,0.014287168,0.00005994503,0.00013773788,0.001916684,0.00040955874,0.0018873924,0.9723474,0.00027080855,0.0031399054,0.00006249034],"about_ca_topic_score_codex":0.0033312598,"about_ca_topic_score_gemma":0.007090599,"teacher_disagreement_score":0.0033312598,"about_ca_system_score_codex":0.00074323174,"about_ca_system_score_gemma":0.0008684058,"threshold_uncertainty_score":0.007928133},"labels":[],"label_agreement":null},{"id":"W3203823955","doi":"10.1016/j.stemcr.2021.09.002","title":"Large-scale analysis of imprinting in naive human pluripotent stem cells reveals recurrent aberrations and a potential link to FGF signaling","year":2021,"lang":"en","type":"article","venue":"Stem Cell Reports","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":18,"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":"Azrieli Foundation; Israel Science Foundation; Rosetrees Trust","keywords":"Biology; Imprinting (psychology); Genomic imprinting; Induced pluripotent stem cell; DNA methylation; Reprogramming; Genetics; Embryonic stem cell; Epigenetics; Genomics; Computational biology; Gene; Genome; Gene expression","score_opus":0.009291860211971608,"score_gpt":0.24166990324657212,"score_spread":0.2323780430346005,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W3203823955","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.991606,0.00049063825,0.006765067,0.00002620452,0.0000059325407,0.00002375677,0.00050548336,0.00006537546,0.0005115514],"genre_scores_gemma":[0.99524814,0.00024090685,0.003169362,0.00002539864,0.0000032533549,0.000021561507,0.00068804104,0.000016934024,0.000586445],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9999069,0.000009490297,0.000008654556,0.00002644062,0.000036617734,0.000011821234],"domain_scores_gemma":[0.99989283,0.000032359483,0.000025184603,0.000022402384,0.0000114949,0.000015824462],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00013923414,0.0001171575,0.000104041465,0.00017875113,0.00008660009,0.0002045775,0.00008808695,0.000107796295,0.0006962758],"category_scores_gemma":[0.00023377803,0.00008762382,0.00010302174,0.00012534134,0.0001363735,0.000088352615,0.00017636517,0.00025007373,0.00016109372],"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":[0.000031063617,0.0000044203575,0.002064502,0.000010685597,0.0000035456028,0.000040539213,0.000015555177,0.000054318232,0.9958967,0.000034124132,0.0000095171445,0.0018349765],"study_design_scores_gemma":[0.0000040839673,0.00015296167,0.07615716,0.000003647954,0.000020417638,0.0004920717,0.000046855777,0.0011553296,0.9207698,0.00014924728,0.0010439135,0.0000045402635],"about_ca_topic_score_codex":0.0002701552,"about_ca_topic_score_gemma":0.00047171343,"teacher_disagreement_score":0.0006962758,"about_ca_system_score_codex":0.00008044699,"about_ca_system_score_gemma":0.00008724363,"threshold_uncertainty_score":0.00232929},"labels":[],"label_agreement":null},{"id":"W3207949079","doi":"","title":"Unique Circumstances and Family Stress: Having a Sibling with Prader-Willi Syndrome","year":2021,"lang":"en","type":"article","venue":"Student Research Proceedings","topic":"Genetic Syndromes and Imprinting","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":"MacEwan University","funders":"","keywords":"Psychology; Sister; Sibling; Developmental psychology; Context (archaeology); Anxiety; Depression (economics); Neglect; Clinical psychology; Medicine; Psychiatry","score_opus":0.04991309114187602,"score_gpt":0.3578921124897909,"score_spread":0.3079790213479149,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W3207949079","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9972615,0.00021833685,0.00008346069,0.0006978555,0.00002529137,0.000009180541,0.000033613316,0.000002990684,0.0016676921],"genre_scores_gemma":[0.99892455,0.00027441737,0.00011954635,0.00014668317,0.000016701855,0.0000056428007,0.000021058586,0.0000014253089,0.0004898734],"study_design_codex":"observational","study_design_gemma":"qualitative","domain_scores_codex":[0.99971765,0.00010007791,0.000015203879,0.00004730291,0.000069756454,0.000049934722],"domain_scores_gemma":[0.9995307,0.00010396328,0.00012407723,0.000021131675,0.00004524341,0.00017487768],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0003065235,0.00025126152,0.0002620154,0.0003464684,0.0012795079,0.00033367044,0.00020254441,0.00032632716,0.0021568749],"category_scores_gemma":[0.0021585308,0.00015981482,0.00016918767,0.00029484578,0.0004699545,0.00041404943,0.00058074424,0.0006353608,0.00016334644],"study_design_candidate":"qualitative","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00012235736,0.0003154631,0.8634093,0.00004233968,0.000057426874,0.10195299,0.009935361,0.00015354487,0.0033840751,0.00070732017,0.0020467124,0.0178732],"study_design_scores_gemma":[0.000022392973,0.0006180054,0.77417034,0.00008719467,0.00007618437,0.19562526,0.02414824,0.00037216346,0.0010855708,0.001318795,0.0024265489,0.000049248498],"about_ca_topic_score_codex":0.006119741,"about_ca_topic_score_gemma":0.01154671,"teacher_disagreement_score":0.006119741,"about_ca_system_score_codex":0.0005026279,"about_ca_system_score_gemma":0.0005267871,"threshold_uncertainty_score":0.012168229},"labels":[],"label_agreement":null},{"id":"W35139074","doi":"10.1371/journal.pgen.1009644","title":"人CYP17基因启动子5＇上游-34碱基处T→C突变与复发性流产","year":2010,"lang":"en","type":"article","venue":"现代妇产科进展","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":0,"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 Neurological Disorders and Stroke; National Institute of General Medical Sciences; Canadian Institutes of Health Research; National Institutes of Health","keywords":"Geology","score_opus":0.005039009677445543,"score_gpt":0.22708826777008523,"score_spread":0.22204925809263967,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W35139074","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.81978434,0.008600392,0.03229006,0.001531454,0.0015568717,0.0008099496,0.050049648,0.004168673,0.08120871],"genre_scores_gemma":[0.61860573,0.0046801893,0.012478311,0.0006150264,0.00020477365,0.00058303215,0.04827592,0.001216246,0.3133408],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9998528,0.000016521664,0.0000051635025,0.00006501004,0.000031820688,0.000028727618],"domain_scores_gemma":[0.99989986,0.00001126593,0.000022369386,0.000019563582,0.000012127776,0.000034776647],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00007547285,0.0005050073,0.00029450023,0.00034963503,0.0004101156,0.00035286928,0.0002479148,0.00026559926,0.03614931],"category_scores_gemma":[0.00007839848,0.0002453405,0.00050814345,0.00035185379,0.00027131932,0.00016553325,0.00022485887,0.00075912056,0.03336388],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00037518327,0.0001052506,0.0032337718,0.00016803062,0.00004478973,0.00056183327,0.00003751913,0.000210716,0.9600842,0.0014350171,0.0046941023,0.029049624],"study_design_scores_gemma":[0.00010421791,0.0005341697,0.03701284,0.000034742734,0.000069954054,0.0018251408,0.000093781324,0.00049704325,0.6536811,0.0004919839,0.3056232,0.000031801646],"about_ca_topic_score_codex":0.0010684003,"about_ca_topic_score_gemma":0.0020146356,"teacher_disagreement_score":0.03614931,"about_ca_system_score_codex":0.00033764512,"about_ca_system_score_gemma":0.00030371637,"threshold_uncertainty_score":0.120931506},"labels":[],"label_agreement":null},{"id":"W4051065","doi":"10.2105/ajph.75.11.1288","title":"Maintenance of germ line and somatic DNA methylation during mouse development","year":2003,"lang":"en","type":"article","venue":"American journal of public health","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":0,"is_retracted":false,"has_abstract":true,"route_ca_aff":false,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":true,"ca_institutions":"","funders":"","keywords":"Genomic imprinting; DNA methylation; Biology; Imprinting (psychology); Genetics; Methylation; RNA-Directed DNA Methylation; Transgene; Epigenetics; Gene; Gene expression","score_opus":0.019194254761217444,"score_gpt":0.2721981206192444,"score_spread":0.253003865858027,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4051065","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.98840535,0.00045285057,0.005583063,0.000060618073,0.0000073210726,0.00005365539,0.0040919757,0.000103698825,0.0012415209],"genre_scores_gemma":[0.98933595,0.00029206206,0.006041759,0.0000353694,0.0000019903284,0.0000440899,0.0025416436,0.000030676554,0.0016764364],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.999526,0.00007181184,0.000033787328,0.00010573016,0.00018099471,0.000081660495],"domain_scores_gemma":[0.9992694,0.00018882744,0.00021556711,0.00011290014,0.00012140368,0.000091874565],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0008041729,0.00018733332,0.00013861009,0.0017744824,0.00030086667,0.00055349065,0.00041515764,0.00017653697,0.0009611012],"category_scores_gemma":[0.00086299994,0.0002287591,0.00029437954,0.0008012188,0.0003004413,0.00011972375,0.00022908825,0.00030480386,0.00018587787],"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":[0.0008641908,0.00013762918,0.4398543,0.00010341249,0.00027467412,0.00042646003,0.00050791143,0.002953767,0.50180966,0.0013025467,0.00061667763,0.051148698],"study_design_scores_gemma":[0.000032806456,0.00032273008,0.86981255,0.000016902639,0.000107995,0.00049988844,0.00016972735,0.00707617,0.11593128,0.0002751717,0.005728607,0.000026164118],"about_ca_topic_score_codex":0.110339545,"about_ca_topic_score_gemma":0.19455324,"teacher_disagreement_score":0.110339545,"about_ca_system_score_codex":0.0015247341,"about_ca_system_score_gemma":0.0012028745,"threshold_uncertainty_score":0.21939462},"labels":[],"label_agreement":null},{"id":"W4200396616","doi":"10.1007/s11657-021-01040-2","title":"Publisher Correction: Exercise for improving age-related hyperkyphosis: a systematic review and meta-analysis with GRADE assessment","year":2021,"lang":"en","type":"review","venue":"Archives of Osteoporosis","topic":"Genetic Syndromes and Imprinting","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":"Research Institute for Aging; University of Waterloo","funders":"","keywords":"Meta-analysis; Medicine; Physical therapy; Physical medicine and rehabilitation; Gerontology; Internal medicine","score_opus":0.03151592619834888,"score_gpt":0.30105692603731293,"score_spread":0.26954099983896407,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4200396616","genre_codex":"editorial","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":[0.0011341888,0.41938365,0.0027429382,0.06512136,0.453012,0.0020923698,0.04873048,0.00094414386,0.0068389615],"genre_scores_gemma":[0.086561434,0.4988871,0.017355777,0.12061256,0.14310795,0.010765781,0.024279647,0.0022659388,0.09616385],"study_design_codex":"not_applicable","study_design_gemma":"meta_analysis","domain_scores_codex":[0.98432356,0.006141693,0.0049302867,0.0011629082,0.0028967494,0.0005447198],"domain_scores_gemma":[0.95771176,0.019783977,0.0073019615,0.0018957519,0.012602082,0.0007043673],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.020173727,0.0028231498,0.00850108,0.005750331,0.0007362387,0.0041520856,0.0043246634,0.0039455756,0.11103955],"category_scores_gemma":[0.14294048,0.0018186155,0.008805555,0.009225352,0.0011323004,0.0028618034,0.0022045749,0.0041553183,0.012928886],"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":[0.0017986828,0.000019991654,0.0010160368,0.263651,0.015468662,0.00033258167,0.00016102604,0.00018399768,0.00012776387,0.00086938275,0.67171955,0.04465119],"study_design_scores_gemma":[0.01864193,0.00039999266,0.01302098,0.23542558,0.118513994,0.0010523268,0.00040129788,0.0007580131,0.0005311587,0.0050661075,0.6057445,0.0004440836],"about_ca_topic_score_codex":0.012926999,"about_ca_topic_score_gemma":0.028163902,"teacher_disagreement_score":0.11103955,"about_ca_system_score_codex":0.002898142,"about_ca_system_score_gemma":0.008451487,"threshold_uncertainty_score":0.3714643},"labels":[],"label_agreement":null},{"id":"W4206219844","doi":"10.1038/npg.els.0005823","title":"Chromosome 14","year":2006,"lang":"en","type":"other","venue":"Encyclopedia of Life Sciences","topic":"Genetic Syndromes and Imprinting","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":"University of Alberta","funders":"","keywords":"Chromosome; Centromere; Gene; Genetics; Biology; Chromosome 22; Genome","score_opus":0.008982955648986138,"score_gpt":0.2428887717947663,"score_spread":0.23390581614578018,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4206219844","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":[0.058068216,0.008246123,0.01963418,0.003014395,0.0024332826,0.0003967492,0.06406705,0.0034588254,0.84068114],"genre_scores_gemma":[0.122777134,0.0035550008,0.017063841,0.0015635106,0.00033020522,0.0002751301,0.090853274,0.00039517717,0.7631867],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.9996989,0.00003347517,0.000012668319,0.00009642619,0.00010467893,0.000054022403],"domain_scores_gemma":[0.99979895,0.000023174067,0.000029459388,0.00001989679,0.00008844069,0.000040113588],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00014976982,0.001220676,0.00051592523,0.0016411382,0.0011207723,0.0012210173,0.00076271826,0.00063070405,0.19966605],"category_scores_gemma":[0.0004968065,0.00022487174,0.0004635484,0.0012156554,0.00032021734,0.0004631637,0.00086770026,0.0007706885,0.09310551],"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":[0.00072761194,0.0002143245,0.013918956,0.00075436535,0.00026688812,0.003292473,0.00030920588,0.0009945845,0.0653763,0.0724192,0.41396767,0.4277584],"study_design_scores_gemma":[0.000037396243,0.00004327759,0.0072870753,0.00009478657,0.000061103456,0.0017510041,0.00004726602,0.00016420786,0.005904555,0.0046040583,0.97998595,0.000019198858],"about_ca_topic_score_codex":0.0032016477,"about_ca_topic_score_gemma":0.0029399265,"teacher_disagreement_score":0.19966605,"about_ca_system_score_codex":0.00072729867,"about_ca_system_score_gemma":0.00074632297,"threshold_uncertainty_score":0.6679495},"labels":[],"label_agreement":null},{"id":"W4206265803","doi":"10.1101/2022.01.10.21268493","title":"Network-based integrative analysis of lithium response in bipolar disorder using transcriptomic and GWAS data","year":2022,"lang":"en","type":"preprint","venue":"medRxiv","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":1,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Dalhousie University","funders":"National Center for Advancing Translational Sciences; National Institute of Mental Health; National Institutes of Health; Genome Atlantic; University of California, San Diego; Dalhousie University; Research Nova Scotia; U.S. Department of Veterans Affairs; Paul G. Allen Frontiers Group; Georgia Clinical and Translational Science Alliance; Dalhousie Medical Research Foundation; JPB Foundation; Canadian Institutes of Health Research; American Heart Association","keywords":"Genome-wide association study; Transcriptome; Computational biology; Biology; Bipolar disorder; Candidate gene; Gene; Gene expression profiling; Gene regulatory network; Genetics; Lithium (medication); Single-nucleotide polymorphism; Gene expression; Endocrinology; Genotype","score_opus":0.032882806206032476,"score_gpt":0.29736505055948925,"score_spread":0.2644822443534568,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4206265803","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9496773,0.0022392224,0.029435448,0.0005666821,0.00004581992,0.000087594046,0.016233927,0.0003073921,0.0014065688],"genre_scores_gemma":[0.9757302,0.00052440254,0.012332107,0.00011354647,0.000028110886,0.000101218444,0.010720908,0.0000457936,0.0004036605],"study_design_codex":"observational","study_design_gemma":"simulation_or_modeling","domain_scores_codex":[0.9995167,0.0001673414,0.000028329358,0.00018926382,0.000054856282,0.000043522086],"domain_scores_gemma":[0.9991037,0.0005147662,0.0001492871,0.000063691936,0.00010239033,0.000066065564],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00086289836,0.00044181565,0.0005813102,0.0020842834,0.0003485345,0.00066269335,0.00033279648,0.00023566687,0.0023883292],"category_scores_gemma":[0.0017383852,0.00015479673,0.0011095945,0.0022002407,0.00018878216,0.00023736853,0.00052539224,0.00043877633,0.00022155429],"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":[0.0012135458,0.00015325748,0.8600625,0.000739462,0.0055958815,0.0009734019,0.00033097144,0.026319558,0.049435362,0.00171795,0.003397312,0.050060775],"study_design_scores_gemma":[0.00005912205,0.00022007224,0.8934276,0.00007290558,0.0020071878,0.0006142024,0.0003231595,0.093288295,0.0022835888,0.0041870545,0.003478831,0.000037994607],"about_ca_topic_score_codex":0.0047599818,"about_ca_topic_score_gemma":0.0062275184,"teacher_disagreement_score":0.0047599818,"about_ca_system_score_codex":0.0003589145,"about_ca_system_score_gemma":0.0004743953,"threshold_uncertainty_score":0.009464502},"labels":[],"label_agreement":null},{"id":"W4210561741","doi":"10.1096/fasebj.22.1_supplement.306.2","title":"Glucose transporter type 2 (GLUT2) genotype is associated with higher intakes of sugars in two distinct populations","year":2008,"lang":"en","type":"article","venue":"The FASEB Journal","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":0,"is_retracted":false,"has_abstract":true,"route_ca_aff":false,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":true,"ca_institutions":"","funders":"","keywords":"GLUT2; Allele; Population; Type 2 diabetes; Genotype; Biology; Medicine; Food intake; Endocrinology; Diabetes mellitus; Internal medicine; Physiology; Genetics; Glucose transporter; Insulin; Gene; Environmental health","score_opus":0.026378080613727255,"score_gpt":0.25799924830692544,"score_spread":0.23162116769319818,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4210561741","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9992059,0.00006909728,0.00030407298,0.000031645963,0.0000068331974,0.0000056899557,0.00009384466,0.0000050442914,0.00027786515],"genre_scores_gemma":[0.99764156,0.00012766881,0.00044310998,0.000060720886,0.000018084696,0.000020419606,0.0002547639,0.000022293785,0.0014113984],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9994647,0.00013948552,0.000045477736,0.00021803658,0.000081377955,0.000050888608],"domain_scores_gemma":[0.9994593,0.00015057354,0.00019564018,0.000057506535,0.00003684794,0.00010019433],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.000400365,0.00081848324,0.0004093237,0.0010534183,0.00048137363,0.00042249117,0.00032219282,0.00051746797,0.0032752808],"category_scores_gemma":[0.0012378602,0.00026386525,0.00034583494,0.00059082446,0.00049908337,0.00020872959,0.00077156455,0.0005488919,0.00020727112],"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":[0.008120976,0.0010563898,0.7798715,0.00009615902,0.0006026514,0.011861423,0.002106879,0.00035381873,0.16833958,0.0016982967,0.0008399109,0.025052471],"study_design_scores_gemma":[0.00015172041,0.0006342814,0.98292345,0.000023191758,0.00019110132,0.009842618,0.0004057843,0.00051164825,0.0040102964,0.0004522577,0.0008201838,0.000033429144],"about_ca_topic_score_codex":0.0017523051,"about_ca_topic_score_gemma":0.0016426523,"teacher_disagreement_score":0.0032752808,"about_ca_system_score_codex":0.00017457429,"about_ca_system_score_gemma":0.00013551873,"threshold_uncertainty_score":0.010956883},"labels":[],"label_agreement":null},{"id":"W4210836986","doi":"10.3410/f.1007260.264660","title":"Faculty Opinions recommendation of Identification of a 3.0-kb major recombination hotspot in patients with Sotos syndrome who carry a common 1.9-Mb microdeletion.","year":2004,"lang":"en","type":"dataset","venue":"Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature","topic":"Genetic Syndromes and Imprinting","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":"University of Toronto","funders":"","keywords":"Breakpoint; Sotos syndrome; Genetics; Haploinsufficiency; Gene; Biology; Craniofacial; Chromosome; Phenotype","score_opus":0.010268431137120185,"score_gpt":0.28909266394488126,"score_spread":0.2788242328077611,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4210836986","genre_codex":"other","genre_gemma":"dataset","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"dataset","genre_consensus":null,"domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.00862579,0.0063532833,0.004558388,0.24848323,0.07041185,0.0010881041,0.016539043,0.0018652738,0.64207494],"genre_scores_gemma":[0.024331136,0.011124078,0.006570891,0.035146836,0.025619728,0.00050374307,0.009926591,0.0006365808,0.8861404],"study_design_codex":"not_applicable","study_design_gemma":"not_applicable","domain_scores_codex":[0.9985789,0.00017707449,0.00013073524,0.00018225271,0.0007613755,0.00016969103],"domain_scores_gemma":[0.98975104,0.00045378576,0.00066003343,0.00039604117,0.006089014,0.0026501801],"candidate_categories":["insufficient_payload"],"consensus_categories":[],"category_scores_codex":[0.001702673,0.0004272187,0.0005012588,0.0017479447,0.0014581644,0.0026869453,0.00075034256,0.002948657,0.31212246],"category_scores_gemma":[0.007910558,0.000331338,0.0004290659,0.001611085,0.0005186867,0.0009429128,0.000930149,0.0016368929,0.15315028],"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":[0.0000690074,0.000058612863,0.0033663483,0.00016342767,0.000008065986,0.00016896329,0.00003713943,0.00004634741,0.0010368527,0.00032826784,0.9170402,0.077676676],"study_design_scores_gemma":[0.000035723708,0.000039488572,0.00900024,0.00023521634,0.000010387084,0.00020519164,0.00015373553,0.000108975415,0.00040977864,0.0004120541,0.9893762,0.000013186057],"about_ca_topic_score_codex":0.0088543445,"about_ca_topic_score_gemma":0.02581662,"teacher_disagreement_score":0.31212246,"about_ca_system_score_codex":0.0015119755,"about_ca_system_score_gemma":0.004115345,"threshold_uncertainty_score":0.9811738},"labels":[],"label_agreement":null},{"id":"W4210985019","doi":"10.1101/2022.02.11.479460","title":"BORIS/CTCFL-mediated chromatin accessibility alterations promote a pro-invasive transcriptional signature in melanoma cells","year":2022,"lang":"en","type":"preprint","venue":"bioRxiv (Cold Spring Harbor Laboratory)","topic":"Genetic Syndromes and Imprinting","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":"McGill University Health Centre; McGill University; Jewish General Hospital","funders":"","keywords":"Ectopic expression; Chromatin; Melanoma; Biology; Transcription factor; Reprogramming; Promoter; Cancer research; Chromatin immunoprecipitation; Phenotype; Transcriptional regulation; Bivalent chromatin; Gene; Cell biology; Gene expression; Chromatin remodeling; Genetics","score_opus":0.011069053623991035,"score_gpt":0.2273465842418269,"score_spread":0.2162775306178359,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4210985019","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9869818,0.0010821657,0.006486576,0.000113572285,0.00005658275,0.000034877376,0.0029038468,0.00031784043,0.0020227018],"genre_scores_gemma":[0.99007004,0.00037606148,0.0031770053,0.0001477034,0.0000120444265,0.000041423118,0.00306028,0.0000691552,0.003046287],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9998503,0.000007917582,0.0000067974042,0.000052173975,0.000048356047,0.000034376273],"domain_scores_gemma":[0.99987054,0.000018942843,0.000030989162,0.000014526531,0.000029012845,0.00003602466],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00011360589,0.0001765649,0.00018438628,0.0002001285,0.00022490004,0.00035862104,0.00010419227,0.00019809863,0.0017298961],"category_scores_gemma":[0.00011685592,0.0001594746,0.00026415044,0.00015080649,0.0001803498,0.00013595671,0.00025383188,0.00050346827,0.00047151023],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00003292652,0.0000049363766,0.00062557857,0.00002431724,0.0000038091089,0.00002104598,0.000014503242,0.000047529047,0.9985304,0.000038377526,0.00007101793,0.00058545615],"study_design_scores_gemma":[0.000014646478,0.000103767554,0.048685722,0.000015065305,0.000019798947,0.00020532559,0.000116028445,0.003028352,0.94187903,0.00015316339,0.0057660853,0.00001306057],"about_ca_topic_score_codex":0.0011951192,"about_ca_topic_score_gemma":0.0020780237,"teacher_disagreement_score":0.0017298961,"about_ca_system_score_codex":0.0002506423,"about_ca_system_score_gemma":0.00018523069,"threshold_uncertainty_score":0.005787134},"labels":[],"label_agreement":null},{"id":"W4211064310","doi":"10.1002/ajmg.c.30267","title":"Beckwith–Wiedemann syndrome","year":2010,"lang":"en","type":"review","venue":"American Journal of Medical Genetics Part C Seminars in Medical Genetics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":297,"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","funders":"","keywords":"Beckwith–Wiedemann syndrome; Genomic imprinting; Imprinting (psychology); Epigenetics; Genetics; Biology; Gene; Untranslated region; Gene expression; Messenger RNA; DNA methylation","score_opus":0.017864193219866785,"score_gpt":0.33544943385092874,"score_spread":0.31758524063106197,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4211064310","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":[0.00074956915,0.99148035,0.00043220457,0.0006894458,0.0005249934,0.000009828476,0.000034661927,0.000038133865,0.0060408423],"genre_scores_gemma":[0.008033503,0.9865546,0.00062211807,0.00095073465,0.00048798436,0.0000160229,0.0001291774,0.000005192085,0.0032007298],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.9998872,0.000016343112,0.000014593563,0.000021032616,0.000040200543,0.00002067524],"domain_scores_gemma":[0.9999287,0.000025103449,0.0000149730095,0.0000024165372,0.000010912113,0.000017718867],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00018644218,0.001051712,0.0009949745,0.0019887865,0.0003274497,0.0004983321,0.0005676351,0.00091798016,0.0033842046],"category_scores_gemma":[0.00040984456,0.00017117022,0.00025680583,0.0015365067,0.00040328945,0.00062602945,0.0005826586,0.0010044278,0.002184731],"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":[0.00006584219,0.000045314435,0.0007173328,0.0036103898,0.00010066716,0.00718517,0.000057254034,0.00019297472,0.0012129906,0.0028826473,0.069220856,0.9147085],"study_design_scores_gemma":[0.000051272065,0.000058246096,0.0032211754,0.002876821,0.00012988996,0.09972132,0.00009642206,0.00010817682,0.0006682714,0.0023203236,0.8907198,0.00002837302],"about_ca_topic_score_codex":0.00095332734,"about_ca_topic_score_gemma":0.0020356975,"teacher_disagreement_score":0.0033842046,"about_ca_system_score_codex":0.0005108555,"about_ca_system_score_gemma":0.00059000676,"threshold_uncertainty_score":0.011321306},"labels":[],"label_agreement":null},{"id":"W4211087283","doi":"10.1002/mgg3.1843","title":"A multidisciplinary approach and consensus statement to establish standards of care for Angelman syndrome","year":2022,"lang":"en","type":"review","venue":"Molecular Genetics & Genomic Medicine","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":68,"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","funders":"Eunice Kennedy Shriver National Institute of Child Health and Human Development; Foundation for Angelman Syndrome Therapeutics; Angelman Syndrome Foundation","keywords":"Medicine; Health care; Angelman syndrome; Intervention (counseling); Multidisciplinary approach; Psychiatry; Psychology; Family medicine","score_opus":0.029301818757621393,"score_gpt":0.33384397302053886,"score_spread":0.3045421542629175,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4211087283","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":[0.010131268,0.026532983,0.20816313,0.64059937,0.03472502,0.038575765,0.0021539028,0.001306109,0.03781245],"genre_scores_gemma":[0.0812207,0.020045515,0.7687879,0.070146,0.0070573837,0.035387374,0.005525707,0.0005584972,0.011270841],"study_design_codex":"not_applicable","study_design_gemma":"not_applicable","domain_scores_codex":[0.7316111,0.14628935,0.06759077,0.008389076,0.037327915,0.00879174],"domain_scores_gemma":[0.68174464,0.06883872,0.024333585,0.011594581,0.17707692,0.03641149],"candidate_categories":["metaresearch"],"consensus_categories":[],"category_scores_codex":[0.2369668,0.0024621028,0.0034716837,0.011456802,0.008437154,0.00988881,0.012236681,0.014696851,0.0058413036],"category_scores_gemma":[0.2426893,0.0019908235,0.006993632,0.0058933953,0.0059110466,0.010051358,0.023907026,0.020514345,0.004132078],"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":[0.00023932138,0.00083065813,0.0074231806,0.014248629,0.0005473518,0.0030616007,0.02428773,0.005000598,0.003020215,0.05820343,0.51579183,0.36734542],"study_design_scores_gemma":[0.00049730664,0.00051823835,0.0063311947,0.052403994,0.00038841285,0.0028725811,0.016819602,0.005450497,0.0016383287,0.07504994,0.83754736,0.00048261674],"about_ca_topic_score_codex":0.008027801,"about_ca_topic_score_gemma":0.009235574,"teacher_disagreement_score":0.2369668,"about_ca_system_score_codex":0.018773342,"about_ca_system_score_gemma":0.12654951,"threshold_uncertainty_score":0.94095576},"labels":[],"label_agreement":null},{"id":"W4211106289","doi":"10.1007/978-3-319-68192-4_9","title":"Syndromic Obesity","year":2017,"lang":"en","type":"book-chapter","venue":"Contemporary Endocrinology","topic":"Genetic Syndromes and Imprinting","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":"University of Alberta Hospital","funders":"","keywords":"Obesity; Medicine; Genetic syndromes; Mutation; Internal medicine; Genetics; Pediatrics; Bioinformatics; Biology; Gene","score_opus":0.03242328646650253,"score_gpt":0.2538936169145437,"score_spread":0.22147033044804118,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4211106289","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":[0.010794951,0.23512359,0.01564738,0.018569808,0.01136127,0.00005610955,0.00034855516,0.00050879817,0.7075895],"genre_scores_gemma":[0.08901085,0.18129376,0.015131749,0.015600574,0.008584577,0.0001452723,0.00073866185,0.0003398704,0.6891547],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.9999336,0.000014340982,0.0000029675004,0.000012478485,0.000025018631,0.000011566616],"domain_scores_gemma":[0.9999585,0.000013516015,0.000004595178,0.00000444041,0.0000070386286,0.000011888674],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00013065127,0.0006001622,0.00024270214,0.00064765965,0.00028639662,0.0005702111,0.00034302322,0.00059898157,0.013753869],"category_scores_gemma":[0.0003321464,0.00013589347,0.00019719837,0.00043591825,0.0007397175,0.00049178745,0.0009792239,0.0013619971,0.00406751],"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":[0.00005990835,0.000045657434,0.0008662354,0.00032029997,0.000017274957,0.0034381072,0.00041329977,0.00021530004,0.003601324,0.2780679,0.2493389,0.46361586],"study_design_scores_gemma":[0.000010895239,0.000024416713,0.00126052,0.00036233588,0.000009503304,0.014266735,0.00017514502,0.00012542597,0.00036260826,0.046787824,0.93660635,0.000008210639],"about_ca_topic_score_codex":0.00055808167,"about_ca_topic_score_gemma":0.0016021621,"teacher_disagreement_score":0.013753869,"about_ca_system_score_codex":0.00030859213,"about_ca_system_score_gemma":0.00038104228,"threshold_uncertainty_score":0.04601127},"labels":[],"label_agreement":null},{"id":"W4214511712","doi":"10.1210/clinem/dgac105","title":"The Efficacy, Safety, and Pharmacology of a Ghrelin O-Acyltransferase Inhibitor for the Treatment of Prader-Willi Syndrome","year":2022,"lang":"en","type":"article","venue":"The Journal of Clinical Endocrinology & Metabolism","topic":"Genetic Syndromes and Imprinting","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":true,"ca_institutions":"Centre Hospitalier Universitaire Sainte-Justine; University of Alberta; Centre Hospitalier de l’Université de Montréal","funders":"Eunice Kennedy Shriver National Institute of Child Health and Human Development; National Institutes of Health; Eli Lilly and Company","keywords":"Placebo; Medicine; Adverse effect; Pharmacodynamics; Internal medicine; Pharmacokinetics; Ghrelin; Appetite; Crossover study; Endocrinology; Obesity; Clinical trial; Pharmacology; Hormone","score_opus":0.03070680707183707,"score_gpt":0.3471978001677184,"score_spread":0.3164909930958813,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4214511712","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99668115,0.0024421562,0.00017741242,0.00010825041,0.00002150427,0.00012225947,0.00006863886,0.000016396665,0.00036208844],"genre_scores_gemma":[0.99747974,0.0014044426,0.00041912115,0.00013029676,0.000065064465,0.00010712707,0.00015581517,0.0000038865123,0.00023455407],"study_design_codex":"randomized_trial","study_design_gemma":"nonrandomized_trial","domain_scores_codex":[0.9997844,0.00010517483,0.000022686532,0.000027432858,0.000034038494,0.00002621109],"domain_scores_gemma":[0.9997037,0.000096414165,0.000096167045,0.000015012888,0.00001711314,0.00007145104],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00063025125,0.00045449633,0.0007664918,0.0002444772,0.0001878576,0.00029807183,0.00038645556,0.0004865157,0.0012941906],"category_scores_gemma":[0.00066542637,0.00021695593,0.0004818561,0.0001767165,0.0005252618,0.00038872313,0.00015343374,0.0012492738,0.0002089552],"study_design_candidate":"nonrandomized_trial","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.35329163,0.0289214,0.034867246,0.0016582874,0.0013405479,0.0011419797,0.0004613562,0.0017651394,0.28111112,0.00024161613,0.0010673661,0.29413226],"study_design_scores_gemma":[0.15537727,0.65887,0.14574443,0.00008707183,0.0010901383,0.001727471,0.00020904443,0.0016069255,0.03205063,0.00009632798,0.0030927942,0.000047913007],"about_ca_topic_score_codex":0.00041034675,"about_ca_topic_score_gemma":0.0010287983,"teacher_disagreement_score":0.0012941906,"about_ca_system_score_codex":0.00032011818,"about_ca_system_score_gemma":0.00047692214,"threshold_uncertainty_score":0.0043295026},"labels":[],"label_agreement":null},{"id":"W4224224823","doi":"10.3390/jcm11082268","title":"Serum Asprosin Concentrations in Children with Prader–Willi Syndrome: Correlations with Metabolic Parameters","year":2022,"lang":"en","type":"article","venue":"Journal of Clinical Medicine","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":4,"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":"Stollery Children’s Hospital Foundation; Canadian Institutes of Health Research; Women and Children's Health Research Institute; Foundation for Prader-Willi Research","keywords":"Medicine; Postprandial; Internal medicine; Endocrinology; Overweight; Obesity; Insulin resistance; Insulin; Leptin; Metabolic syndrome; Adipose tissue","score_opus":0.023468248629222126,"score_gpt":0.31687579950565775,"score_spread":0.2934075508764356,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4224224823","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9994301,0.00027017054,0.000058119425,0.00001565566,0.0000029964672,0.0000035081698,0.00010975502,0.000003993798,0.00010564292],"genre_scores_gemma":[0.99928683,0.00021248778,0.00020779645,0.000012372177,0.000007286828,0.000008214512,0.00018179498,0.0000023132206,0.00008099897],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9997011,0.000059096594,0.000047286965,0.00008967399,0.000062279665,0.000040486742],"domain_scores_gemma":[0.99911016,0.00018328715,0.00046107176,0.00004255233,0.000057278547,0.00014566872],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00029526153,0.00055941864,0.0004954323,0.0009757534,0.00023170079,0.00036967383,0.00021601345,0.00044562857,0.001023332],"category_scores_gemma":[0.0014729566,0.00038296345,0.0002876357,0.00072925206,0.00032688922,0.00039356752,0.00036870965,0.00058606366,0.000174844],"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":[0.00014653827,0.000015109438,0.9976494,0.000010873066,0.000027039183,0.00028556577,0.0000422777,0.000029243103,0.0009135281,0.000008265152,0.00002765256,0.0008445503],"study_design_scores_gemma":[0.000005082233,0.00011836458,0.9981901,0.00000351633,0.000017528962,0.0012803726,0.000084574414,0.00008806415,0.00013994575,0.000010077063,0.000059800444,0.0000025366119],"about_ca_topic_score_codex":0.0018412434,"about_ca_topic_score_gemma":0.001609011,"teacher_disagreement_score":0.0018412434,"about_ca_system_score_codex":0.00018730815,"about_ca_system_score_gemma":0.00016402836,"threshold_uncertainty_score":0.0036610365},"labels":[],"label_agreement":null},{"id":"W4225123264","doi":"10.1371/journal.pgen.1010186","title":"Subnuclear localisation is associated with gene expression more than parental origin at the imprinted Dlk1-Dio3 locus","year":2022,"lang":"en","type":"article","venue":"PLoS Genetics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":2,"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; Canadian Institutes of Health Research; Deutsche Forschungsgemeinschaft; Wellcome Trust","keywords":"Biology; Imprinting (psychology); Genomic imprinting; Allele; Locus (genetics); Genetics; Gene; Mutant; Gene expression; Cell biology; DNA methylation","score_opus":0.01517431627127163,"score_gpt":0.22800009878546648,"score_spread":0.21282578251419484,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4225123264","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99270684,0.00060548744,0.0050114878,0.00005696075,0.000012051951,0.0000053980475,0.00032366256,0.00008561258,0.0011924561],"genre_scores_gemma":[0.9962368,0.00024141886,0.0013747422,0.00001878583,0.0000020850084,0.0000064501637,0.00024233646,0.000033735356,0.0018436752],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9998423,0.000010698231,0.0000132557825,0.00006720328,0.000044237804,0.000022298154],"domain_scores_gemma":[0.9997769,0.000034664037,0.000097918055,0.000024299532,0.000011018775,0.0000551727],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00007865818,0.00022208852,0.00016083142,0.00029538767,0.00011249672,0.0003342193,0.00016663372,0.00020718123,0.0019244483],"category_scores_gemma":[0.0001290839,0.00017460743,0.00013285103,0.0001637352,0.0003289488,0.00017527415,0.0002898769,0.0004143728,0.0004157408],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.000026171037,0.0000017504148,0.0005284111,0.000009974766,0.000001548414,0.00003709767,0.000008741797,0.000016996346,0.9988938,0.000057364643,0.0000039760816,0.00041422085],"study_design_scores_gemma":[0.000007045665,0.000044138378,0.051037975,0.00000382469,0.000011603904,0.00068362535,0.00004608463,0.00043462965,0.94640744,0.00009539646,0.0012227119,0.000005579515],"about_ca_topic_score_codex":0.0006420577,"about_ca_topic_score_gemma":0.0014365051,"teacher_disagreement_score":0.0019244483,"about_ca_system_score_codex":0.00031216315,"about_ca_system_score_gemma":0.00013173286,"threshold_uncertainty_score":0.0064379573},"labels":[],"label_agreement":null},{"id":"W4225308711","doi":"10.1164/ajrccm-conference.2022.205.1_meetingabstracts.a3002","title":"The Presence of 14 and 6 Hz Spike Wave Activity in Children with Prader Willi Syndrome","year":2022,"lang":"en","type":"article","venue":"","topic":"Genetic Syndromes and Imprinting","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":"Hospital for Sick Children; SickKids Foundation","funders":"","keywords":"Spike (software development); Audiology; Computer science; Psychology; Neuroscience; Medicine","score_opus":0.006450644347144715,"score_gpt":0.20544277638527714,"score_spread":0.19899213203813243,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4225308711","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99873704,0.00011330454,0.00016313505,0.000047804933,0.000011001911,0.0000040369764,0.00012474082,0.000016758831,0.00078222266],"genre_scores_gemma":[0.9992968,0.00012858649,0.00024434167,0.000020520165,0.000015992771,0.0000060180464,0.000096821714,0.000007197591,0.00018364965],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99959546,0.00006949987,0.000047541507,0.000078535646,0.0001274239,0.000081632286],"domain_scores_gemma":[0.9989723,0.00040766122,0.0003432145,0.000041733085,0.00007876893,0.00015636116],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00026882865,0.0004944826,0.00040208158,0.001809993,0.00029888368,0.00042560537,0.00037340223,0.00053354306,0.0020490063],"category_scores_gemma":[0.0026150567,0.00028750408,0.00022696286,0.00071305904,0.000754374,0.00033247587,0.0004685902,0.00053389714,0.00022481965],"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":[0.0008601901,0.00012609626,0.86514336,0.00010994054,0.00007964191,0.05203054,0.0015933929,0.0003269812,0.06922646,0.00047191023,0.00033846797,0.009692966],"study_design_scores_gemma":[0.000022262964,0.00032761536,0.9242964,0.000013847971,0.000071009235,0.06848983,0.0008616711,0.00034169084,0.0048406203,0.00020866038,0.0005065723,0.000019927751],"about_ca_topic_score_codex":0.0019285933,"about_ca_topic_score_gemma":0.001369977,"teacher_disagreement_score":0.0020490063,"about_ca_system_score_codex":0.00014026434,"about_ca_system_score_gemma":0.00028097018,"threshold_uncertainty_score":0.0068545938},"labels":[],"label_agreement":null},{"id":"W4229587581","doi":"10.1139/gen-44-3-311","title":"Imprinting and deviation from Mendelian transmission ratios","year":2001,"lang":"en","type":"article","venue":"Genome","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":4,"is_retracted":false,"has_abstract":false,"route_ca_aff":false,"route_ca_fund":false,"route_ca_venue":true,"route_about_ca":false,"ca_institutions":"","funders":"","keywords":"Imprinting (psychology); Biology; Mendelian inheritance; Genetics; Genomic imprinting; Evolutionary biology; Gene; DNA methylation","score_opus":0.009623054575879447,"score_gpt":0.22403843145084426,"score_spread":0.2144153768749648,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4229587581","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9147381,0.00939203,0.04473887,0.0035595347,0.00026503147,0.000023997876,0.00067313184,0.00080471725,0.02580457],"genre_scores_gemma":[0.99596405,0.0012168295,0.0018715409,0.00005727046,0.000046759018,0.0000075143057,0.00006217468,0.000028433193,0.00074537145],"study_design_codex":"theoretical_or_conceptual","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99935156,0.00026888162,0.000037663634,0.000108902925,0.00018262453,0.00005042413],"domain_scores_gemma":[0.9985696,0.00089345174,0.0002674179,0.00012019755,0.00005323753,0.00009616913],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00061295205,0.0004433218,0.0004584442,0.0009861051,0.0001807642,0.00064848945,0.00052709645,0.00042898694,0.0030798668],"category_scores_gemma":[0.0044244844,0.00020717827,0.00016198277,0.0006187803,0.00090808864,0.0004855803,0.00033017885,0.0007181882,0.0003707722],"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":[0.0033493526,0.0001322721,0.09843235,0.00036821386,0.00044313952,0.014912705,0.00088520325,0.012412171,0.3078297,0.38966933,0.0042059943,0.16735965],"study_design_scores_gemma":[0.00045498495,0.00065808144,0.2099383,0.00007243512,0.0004275395,0.09143937,0.0005612948,0.031181803,0.25334194,0.38783643,0.02387926,0.00020857426],"about_ca_topic_score_codex":0.00042138709,"about_ca_topic_score_gemma":0.00020569847,"teacher_disagreement_score":0.0030798668,"about_ca_system_score_codex":0.00034013833,"about_ca_system_score_gemma":0.00019637878,"threshold_uncertainty_score":0.01030314},"labels":[],"label_agreement":null},{"id":"W4232227875","doi":"10.14740/jem337w","title":"Clinical and Genetic Study of Pseudohypoparathyroidism Type 1b in Hong Kong Chinese","year":2016,"lang":"en","type":"article","venue":"Journal of Endocrinology and Metabolism","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":2,"is_retracted":false,"has_abstract":true,"route_ca_aff":false,"route_ca_fund":false,"route_ca_venue":true,"route_about_ca":false,"ca_institutions":"","funders":"","keywords":"GNAS complex locus; Pseudohypoparathyroidism; Medicine; Imprinting (psychology); Uniparental disomy; Multiplex ligation-dependent probe amplification; Genetics; Chinese population; Locus (genetics); Gene; Bioinformatics; Chromosome; Parathyroid hormone; Internal medicine; Karyotype; Biology; Genotype; Exon","score_opus":0.016792506397998935,"score_gpt":0.30657542035166213,"score_spread":0.2897829139536632,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4232227875","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99936503,0.00012401289,0.00005007383,0.000038825947,0.000003435918,0.000013063437,0.000048587684,0.0000015888454,0.00035532718],"genre_scores_gemma":[0.9995228,0.0001120585,0.000042239266,0.000027596821,0.0000046495707,0.000004292713,0.000046142435,0.0000013335238,0.00023890314],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9997677,0.00002783542,0.000036656937,0.00007189486,0.000042297674,0.000053543612],"domain_scores_gemma":[0.99962866,0.000065499305,0.00006902954,0.000021742206,0.000046778954,0.00016824734],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00021594428,0.00045496406,0.00042166232,0.0011677503,0.0012795407,0.0003173384,0.0002730484,0.00037257056,0.0012261763],"category_scores_gemma":[0.0007031146,0.00035511176,0.00026962822,0.0013304176,0.0005964413,0.00026226556,0.00045555836,0.00026535752,0.00012375716],"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":[0.00014803308,0.000088168286,0.9202971,0.000049974584,0.00004301883,0.068746,0.002410995,0.0001121956,0.005304468,0.000114872884,0.00019697401,0.0024883328],"study_design_scores_gemma":[0.000017463019,0.00016349426,0.95949405,0.000013652024,0.00005385713,0.03746125,0.0014843475,0.00031545616,0.00044377084,0.000060667873,0.00047233756,0.000019694886],"about_ca_topic_score_codex":0.089108266,"about_ca_topic_score_gemma":0.043796636,"teacher_disagreement_score":0.089108266,"about_ca_system_score_codex":0.00095585163,"about_ca_system_score_gemma":0.00080076087,"threshold_uncertainty_score":0.17717916},"labels":[],"label_agreement":null},{"id":"W4235369933","doi":"10.1139/gen-43-2-285","title":"Varied expression of a Y-linked P[&lt;i&gt;w&lt;/i&gt;&lt;sup&gt;+&lt;/sup&gt;] insert due to imprinting in &lt;i&gt;Drosophila melanogaster&lt;/i&gt;","year":2000,"lang":"en","type":"article","venue":"Genome","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":0,"is_retracted":false,"has_abstract":false,"route_ca_aff":false,"route_ca_fund":false,"route_ca_venue":true,"route_about_ca":false,"ca_institutions":"","funders":"","keywords":"Biology; Drosophila melanogaster; Genetics; Molecular biology; Imprinting (psychology); Gene","score_opus":0.009955639820608242,"score_gpt":0.22337404346120782,"score_spread":0.21341840364059958,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4235369933","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9398227,0.0016912498,0.038535934,0.00077002216,0.00040111848,0.00020600781,0.0070860116,0.0014452112,0.010041858],"genre_scores_gemma":[0.9576301,0.00064296793,0.013817107,0.00030805517,0.000053222007,0.00015475531,0.008868017,0.0013548187,0.017171055],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9996074,0.000051025632,0.000050654922,0.00014886435,0.000060955063,0.00008110087],"domain_scores_gemma":[0.99922216,0.00027626476,0.00016543076,0.00014506295,0.000041026215,0.00015011405],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00024669012,0.0009659376,0.00036306394,0.0007324758,0.00034633285,0.0005869486,0.0007444258,0.0008231771,0.0053716586],"category_scores_gemma":[0.00038263484,0.0006802622,0.0007738228,0.0005044343,0.0008290396,0.00047209059,0.0008445957,0.0023782493,0.0022265974],"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":[0.000116280244,0.000026500977,0.000085188956,0.000032625525,0.000010576321,0.00008593812,0.00002508301,0.000054198114,0.9982936,0.00035697196,0.000094347655,0.0008187492],"study_design_scores_gemma":[0.000034657874,0.00010114167,0.003145231,0.000012066249,0.00003937843,0.00024448257,0.00003838656,0.00056386157,0.9919906,0.000080652404,0.0037356226,0.000014008871],"about_ca_topic_score_codex":0.00230897,"about_ca_topic_score_gemma":0.004094847,"teacher_disagreement_score":0.0053716586,"about_ca_system_score_codex":0.0007818618,"about_ca_system_score_gemma":0.0004978136,"threshold_uncertainty_score":0.017969966},"labels":[],"label_agreement":null},{"id":"W4239765192","doi":"10.3410/f.717960858.793463732","title":"Faculty Opinions recommendation of Homeotic arm-to-leg transformation associated with genomic rearrangements at the PITX1 locus.","year":2012,"lang":"en","type":"dataset","venue":"Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature","topic":"Genetic Syndromes and Imprinting","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":"Western University","funders":"","keywords":"Locus (genetics); Homeotic gene; Genetics; Transformation (genetics); Biology; Computational biology; Gene","score_opus":0.022390570867623954,"score_gpt":0.30961445852962904,"score_spread":0.2872238876620051,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4239765192","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":[0.00017818346,0.00010005228,0.000039942803,0.000047642436,0.000014049687,0.000006347304,0.99904233,0.0001983249,0.00037313608],"genre_scores_gemma":[0.00070575794,0.000102622515,0.00018433196,0.00005600969,0.000006396516,0.000037577993,0.9982609,0.000053946034,0.00059243274],"study_design_codex":"not_applicable","study_design_gemma":"not_applicable","domain_scores_codex":[0.99888414,0.00014832288,0.00014486033,0.00039262036,0.00027122925,0.00015874178],"domain_scores_gemma":[0.99674356,0.0011083464,0.0005294005,0.00058726507,0.000553754,0.0004777474],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0009976442,0.0019757939,0.0018838008,0.0036683625,0.00067099545,0.002489429,0.0025636896,0.002109484,0.08156538],"category_scores_gemma":[0.0077906693,0.000603975,0.0017910703,0.005354045,0.00030349754,0.0009832953,0.0015702081,0.0015391397,0.060340453],"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":[0.0002629559,0.000034581964,0.0044621364,0.0021241393,0.00018335585,0.00007326995,0.000021658885,0.0003177594,0.00035035735,0.0002905393,0.98723096,0.0046484116],"study_design_scores_gemma":[0.0008680924,0.00004813571,0.02467408,0.0008482662,0.00032884342,0.00023861321,0.000072989635,0.0007526917,0.0009831684,0.0010497819,0.9700814,0.000053914166],"about_ca_topic_score_codex":0.023299642,"about_ca_topic_score_gemma":0.050053935,"teacher_disagreement_score":0.08156538,"about_ca_system_score_codex":0.0010498835,"about_ca_system_score_gemma":0.0025826243,"threshold_uncertainty_score":0.2728634},"labels":[],"label_agreement":null},{"id":"W4243593601","doi":"10.3410/f.13491969.14870064","title":"Faculty Opinions recommendation of Using iPSC-derived neurons to uncover cellular phenotypes associated with Timothy syndrome.","year":2012,"lang":"en","type":"dataset","venue":"Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature","topic":"Genetic Syndromes and Imprinting","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 Calgary","funders":"","keywords":"Phenotype; Neuroscience; Computational biology; Biology; Psychology; Genetics; Gene","score_opus":0.02783178862621694,"score_gpt":0.3116417928913443,"score_spread":0.28381000426512737,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4243593601","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":[0.00018320451,0.00009038895,0.00007875088,0.00011153863,0.00002621333,0.000013293317,0.99832064,0.0003474302,0.0008285157],"genre_scores_gemma":[0.00064534874,0.00010654796,0.0003644286,0.00011481534,0.000010922211,0.000057758498,0.9975865,0.00006867061,0.0010450174],"study_design_codex":"not_applicable","study_design_gemma":"not_applicable","domain_scores_codex":[0.99914074,0.00012697227,0.00010315195,0.00023941818,0.00027819807,0.000111471534],"domain_scores_gemma":[0.9966319,0.0010407433,0.00041738976,0.0007304469,0.0006451165,0.00053443544],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0013764676,0.001648198,0.0013303808,0.003085679,0.0005567996,0.0023852126,0.002156334,0.0020824247,0.092285015],"category_scores_gemma":[0.007423673,0.0005640333,0.0013647947,0.0034817464,0.0002805371,0.0010825904,0.0016074405,0.0013366045,0.07400378],"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":[0.00012424204,0.000021800488,0.0017978391,0.0009016459,0.000065677385,0.000035225818,0.000010871025,0.00017075201,0.00028669692,0.00020589004,0.99260557,0.0037737763],"study_design_scores_gemma":[0.0005809151,0.00004065751,0.011005947,0.00045702336,0.00016367127,0.00012497601,0.000035855774,0.000828827,0.0012990363,0.001054906,0.98436683,0.000041247236],"about_ca_topic_score_codex":0.01266857,"about_ca_topic_score_gemma":0.040652122,"teacher_disagreement_score":0.092285015,"about_ca_system_score_codex":0.00096612534,"about_ca_system_score_gemma":0.0022782572,"threshold_uncertainty_score":0.3087241},"labels":[],"label_agreement":null},{"id":"W4245234573","doi":"10.1172/jci200319159","title":"Autosomal dominant pseudohypoparathyroidism type Ib is associated with a heterozygous microdeletion that likely disrupts a putative imprinting control element of GNAS","year":2003,"lang":"en","type":"article","venue":"Journal of Clinical Investigation","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":24,"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; St. Michael's Hospital; McGill University","funders":"National Institute of Diabetes and Digestive and Kidney Diseases; Canadian Institutes of Health Research; National Institutes of Health","keywords":"GNAS complex locus; Pseudohypoparathyroidism; Imprinting (psychology); Genomic imprinting; Genetics; Biology; Endocrinology; Internal medicine; Medicine; Gene; Parathyroid hormone","score_opus":0.038505553832486036,"score_gpt":0.3210772784450016,"score_spread":0.28257172461251556,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4245234573","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.98766035,0.0014347754,0.002605842,0.0006088757,0.000096988995,0.00007585613,0.00066911237,0.00024499436,0.006603137],"genre_scores_gemma":[0.99691427,0.00043957142,0.0011397501,0.000086027925,0.000086014625,0.000019701294,0.00020738751,0.000029142017,0.0010780697],"study_design_codex":"case_report","study_design_gemma":"observational","domain_scores_codex":[0.99971646,0.000033628232,0.00003029956,0.00007379042,0.000092068665,0.000053697084],"domain_scores_gemma":[0.99939954,0.00017707031,0.00026286306,0.000029308403,0.000015475685,0.00011580571],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00014406549,0.0015174898,0.00058204035,0.0013428695,0.0004858282,0.00042411961,0.00066304044,0.0012709728,0.00301088],"category_scores_gemma":[0.001184197,0.00042749877,0.00033313074,0.0013640599,0.001085222,0.00027200233,0.0005374882,0.0007144075,0.00057228445],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0007641109,0.00008640927,0.038355555,0.00020728527,0.00012702237,0.7993055,0.00029471898,0.0002344506,0.1472294,0.0013533441,0.0009585597,0.011083696],"study_design_scores_gemma":[0.00006667515,0.0002911632,0.06826382,0.000019161338,0.00008712225,0.92024547,0.00010036493,0.00035799888,0.008482209,0.0005275468,0.0015348784,0.00002354746],"about_ca_topic_score_codex":0.0017239641,"about_ca_topic_score_gemma":0.0019141737,"teacher_disagreement_score":0.00301088,"about_ca_system_score_codex":0.0004022685,"about_ca_system_score_gemma":0.00035103897,"threshold_uncertainty_score":0.0100723505},"labels":[],"label_agreement":null},{"id":"W4245280555","doi":"10.1002/ajmg.c.30058","title":"Beckwith–Wiedemann syndrome","year":2005,"lang":"en","type":"article","venue":"American Journal of Medical Genetics Part C Seminars in Medical Genetics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":261,"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; Hospital for Sick Children","funders":"","keywords":"Beckwith–Wiedemann syndrome; Epigenetics; Genomic imprinting; Biology; Genetics; Monozygotic twin; Wilms' tumor; Phenotype; Bioinformatics; DNA methylation; Gene","score_opus":0.008731687724892948,"score_gpt":0.28627210111506673,"score_spread":0.27754041339017377,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4245280555","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9070576,0.017774178,0.007873875,0.003794667,0.0011298631,0.00018472516,0.0016532746,0.00074047927,0.05979141],"genre_scores_gemma":[0.98434955,0.005200848,0.004045313,0.0009800453,0.00017782665,0.00004790871,0.00042020998,0.00004452332,0.0047338186],"study_design_codex":"case_report","study_design_gemma":"case_report","domain_scores_codex":[0.9997503,0.000034988592,0.000018110757,0.00006360237,0.00006860542,0.00006429896],"domain_scores_gemma":[0.9998266,0.00003527213,0.00004649181,0.0000076008646,0.000009791195,0.00007425701],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00011929129,0.0013165196,0.00038256298,0.0013746284,0.00082392804,0.0004488777,0.00023363564,0.0008643014,0.006318968],"category_scores_gemma":[0.0008635293,0.00024958447,0.00029121342,0.00092779193,0.0005688838,0.0003411815,0.000698228,0.00056399725,0.00082942046],"study_design_candidate":"case_report","study_design_consensus":"case_report","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00043609663,0.000106920226,0.077599004,0.00036459067,0.00029220263,0.767982,0.0006537502,0.00064850715,0.04070152,0.017722838,0.015543811,0.07794884],"study_design_scores_gemma":[0.00003998477,0.0001286,0.044363577,0.00017810194,0.000140106,0.93038625,0.0001921606,0.00033626927,0.0042855837,0.0028462023,0.017049257,0.00005378595],"about_ca_topic_score_codex":0.0017553513,"about_ca_topic_score_gemma":0.0021947161,"teacher_disagreement_score":0.006318968,"about_ca_system_score_codex":0.00029574838,"about_ca_system_score_gemma":0.00040123175,"threshold_uncertainty_score":0.021139026},"labels":[],"label_agreement":null},{"id":"W4245435215","doi":"10.1016/j.jpeds.2008.12.032","title":"Reply","year":2009,"lang":"en","type":"article","venue":"The Journal of Pediatrics","topic":"Genetic Syndromes and Imprinting","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":"Medicine; Observational study; Jury; Clinical endpoint; Randomized controlled trial; Pediatrics; Body mass index; Idiopathic short stature; Obesity; Food and drug administration; Clinical trial; Growth hormone; Short stature; Internal medicine; Hormone; Medical emergency","score_opus":0.008040849730539847,"score_gpt":0.23761835483085902,"score_spread":0.22957750510031918,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4245435215","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":[0.00019987464,0.0022007828,0.000062681254,0.9155696,0.0805343,0.0000060086177,0.000053624397,0.000019608227,0.0013535143],"genre_scores_gemma":[0.0015914498,0.0008496515,0.00007754066,0.9539649,0.035661448,0.00002343376,0.000031818796,0.000015582791,0.007784215],"study_design_codex":"not_applicable","study_design_gemma":"not_applicable","domain_scores_codex":[0.9972384,0.0005272724,0.0003309551,0.00054763455,0.0008196548,0.00053604477],"domain_scores_gemma":[0.9864413,0.0053666285,0.0009685796,0.0005206803,0.00391751,0.0027852736],"candidate_categories":["insufficient_payload"],"consensus_categories":[],"category_scores_codex":[0.0030620233,0.0007320421,0.0011109842,0.0010482286,0.0030074983,0.004205839,0.0021053776,0.033671066,0.014177964],"category_scores_gemma":[0.031358566,0.00072036934,0.0011805575,0.00072691235,0.0026834079,0.0040318863,0.003317986,0.040697366,0.010630969],"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":[0.000019099274,0.0000060374105,0.00037580504,0.000028441313,0.000009860037,0.00029359714,0.00007915402,0.000009763928,0.000054004307,0.0011308297,0.9951356,0.0028578714],"study_design_scores_gemma":[0.000041293762,0.000018028555,0.001197921,0.0001437996,0.000026932576,0.000811806,0.000489338,0.00003844317,0.00012924986,0.0022355507,0.9948264,0.00004125121],"about_ca_topic_score_codex":0.0040965937,"about_ca_topic_score_gemma":0.0055362307,"teacher_disagreement_score":0.985822,"about_ca_system_score_codex":0.0025638968,"about_ca_system_score_gemma":0.0038464826,"threshold_uncertainty_score":0},"labels":[],"label_agreement":null},{"id":"W4249491592","doi":"10.1126/science.330.6005.771","title":"2010 Grand Prize Winner","year":2010,"lang":"en","type":"article","venue":"Science","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":0,"is_retracted":false,"has_abstract":true,"route_ca_aff":false,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":true,"ca_institutions":"","funders":"","keywords":"Philosophy","score_opus":0.006707372463534485,"score_gpt":0.239318066395827,"score_spread":0.23261069393229253,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4249491592","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":[0.0026858468,0.010546845,0.0013333376,0.15521173,0.38100633,0.00030452837,0.003352514,0.0006567401,0.44490206],"genre_scores_gemma":[0.004657994,0.0033369076,0.00047679778,0.011976428,0.016281815,0.00011374682,0.0015938377,0.00023685698,0.9613256],"study_design_codex":"not_applicable","study_design_gemma":"not_applicable","domain_scores_codex":[0.9988606,0.00008088493,0.00005156198,0.0001896692,0.00052309444,0.00029424764],"domain_scores_gemma":[0.997417,0.000076610224,0.00006416364,0.000109945235,0.0010468576,0.001285447],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0014921302,0.0013299374,0.00086350454,0.0010972196,0.0022352831,0.00600033,0.0012387708,0.0045195543,0.21569726],"category_scores_gemma":[0.0032817351,0.00029383443,0.0007684668,0.0006798406,0.0007089596,0.0021232995,0.0031049778,0.0035177239,0.19062],"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":[0.000024694373,0.000013106005,0.00006882587,0.000030483448,0.000003116127,0.000046334153,0.000007662123,0.000022485598,0.000108501685,0.0019023261,0.9827716,0.015000931],"study_design_scores_gemma":[0.0000068832296,0.000017585107,0.00032359222,0.000028878972,0.000002183556,0.000043855423,0.000028785458,0.000037873946,0.00007740452,0.0008342465,0.998594,0.0000047825743],"about_ca_topic_score_codex":0.0022907974,"about_ca_topic_score_gemma":0.006422754,"teacher_disagreement_score":0.21569726,"about_ca_system_score_codex":0.002424891,"about_ca_system_score_gemma":0.003931342,"threshold_uncertainty_score":0.7215792},"labels":[],"label_agreement":null},{"id":"W4252671102","doi":"10.1136/adc.88.suppl_1.a70","title":"Metabolic diseases","year":2003,"lang":"en","type":"article","venue":"Archives of Disease in Childhood","topic":"Genetic Syndromes and Imprinting","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":"Hospital for Sick Children","funders":"","keywords":"Medicine; Hypotonia; Internal medicine; Endocrinology; Cytochrome c oxidase; Muscle biopsy; Mitochondrion; Biopsy; Biochemistry; Biology","score_opus":0.004642183146264477,"score_gpt":0.2188441076969611,"score_spread":0.21420192455069664,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4252671102","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":[0.7548709,0.051552232,0.023480486,0.010292583,0.0013681137,0.00054504175,0.009114515,0.0012349144,0.1475413],"genre_scores_gemma":[0.91481525,0.016562657,0.017532276,0.0034950722,0.0005983913,0.00028572098,0.0036669844,0.00019340962,0.042850368],"study_design_codex":"observational","study_design_gemma":"not_applicable","domain_scores_codex":[0.99981993,0.00002753753,0.000018894578,0.000053547734,0.000038319675,0.00004171328],"domain_scores_gemma":[0.9998617,0.000026429794,0.000046993555,0.000014660062,0.000020377604,0.000029773686],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00016342963,0.0009134758,0.00036805225,0.0006567201,0.00039963002,0.00040251,0.00038200503,0.00062436436,0.010826453],"category_scores_gemma":[0.00050196383,0.00014581821,0.00027996852,0.000618472,0.00030115622,0.00022256633,0.0004053513,0.0006476207,0.0027403713],"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":[0.0011284858,0.00039374302,0.3841896,0.0014602126,0.00034352276,0.2459224,0.00054333365,0.00056643266,0.038882606,0.011152812,0.023338187,0.29207873],"study_design_scores_gemma":[0.00011623842,0.00031665052,0.15865587,0.00044843485,0.00015922172,0.71732724,0.00030268385,0.0003766791,0.011660226,0.002131738,0.10845847,0.00004661739],"about_ca_topic_score_codex":0.001240803,"about_ca_topic_score_gemma":0.0015586851,"teacher_disagreement_score":0.010826453,"about_ca_system_score_codex":0.00025292355,"about_ca_system_score_gemma":0.00036946722,"threshold_uncertainty_score":0.036218047},"labels":[],"label_agreement":null},{"id":"W4255496423","doi":"10.1016/s1701-2163(16)35026-5","title":"San Pedro","year":2011,"lang":"en","type":"article","venue":"Journal of Obstetrics and Gynaecology Canada","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":0,"is_retracted":false,"has_abstract":false,"route_ca_aff":false,"route_ca_fund":false,"route_ca_venue":true,"route_about_ca":false,"ca_institutions":"","funders":"","keywords":"Medicine; Pregnancy; Obstetrics; Pediatrics; Gestational age; Macroglossia; Prenatal diagnosis; Epidemiology; Population; Live birth; Fetus; Internal medicine; Tongue; Pathology","score_opus":0.01296928004640372,"score_gpt":0.20728454478738376,"score_spread":0.19431526474098004,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4255496423","genre_codex":"other","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":[0.008038916,0.03476637,0.0007904571,0.007190804,0.005486402,0.00016536725,0.008062005,0.0007832623,0.93471646],"genre_scores_gemma":[0.013746239,0.012422281,0.0013848332,0.0012352593,0.0007020316,0.000058902486,0.002019781,0.00025071178,0.9681798],"study_design_codex":"not_applicable","study_design_gemma":"case_report","domain_scores_codex":[0.9993961,0.00007119809,0.000022723052,0.00019327289,0.00016596241,0.00015070077],"domain_scores_gemma":[0.99920064,0.00009945544,0.0000797691,0.000054551005,0.00026791298,0.0002977048],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00034362858,0.0013497762,0.00072567275,0.0023272932,0.0020221157,0.0020621547,0.00084875984,0.0015774957,0.554947],"category_scores_gemma":[0.001334732,0.00048555256,0.00042715963,0.002057346,0.00055541034,0.00053026056,0.001386837,0.0016866447,0.2564035],"study_design_candidate":"case_report","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00054835645,0.00015703276,0.004735444,0.0010954998,0.000062654886,0.0029970969,0.00023455631,0.0004168721,0.0014738532,0.00882868,0.58927745,0.39017248],"study_design_scores_gemma":[0.00006736609,0.00003701072,0.005323598,0.0003405464,0.000019932873,0.0014808548,0.0001973684,0.00011634779,0.00023303724,0.0005940444,0.9915794,0.000010468585],"about_ca_topic_score_codex":0.056113552,"about_ca_topic_score_gemma":0.15530293,"teacher_disagreement_score":0.554947,"about_ca_system_score_codex":0.0021728168,"about_ca_system_score_gemma":0.004112629,"threshold_uncertainty_score":0},"labels":[],"label_agreement":null},{"id":"W4280526296","doi":"10.1101/2022.04.21.488764","title":"Conservation and divergence of canonical and non-canonical imprinting in murids","year":2022,"lang":"en","type":"preprint","venue":"bioRxiv (Cold Spring Harbor Laboratory)","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":1,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"BC Children's Hospital; University of British Columbia","funders":"NODAI Genome Research Center, Tokyo University of Agriculture; Japan Society for the Promotion of Science; Natural Sciences and Engineering Research Council of Canada; Canadian Institutes of Health Research; Provincial Health Services Authority; Children's Hospital Foundation; Keio University; Fondation pour la Recherche Médicale; Tokyo University of Agriculture; BC Children's Hospital; Sumitomo Foundation","keywords":"Genomic imprinting; Imprinting (psychology); Biology; Gene; Genetics; DNA methylation; Promoter; Genome; Epigenetics; Gene expression","score_opus":0.009617956130026048,"score_gpt":0.22313069120822085,"score_spread":0.2135127350781948,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4280526296","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9954203,0.0011409844,0.0023102276,0.000011089257,0.0000036655638,0.0000048753636,0.00032070468,0.000046631092,0.00074155995],"genre_scores_gemma":[0.99649733,0.0003122358,0.0017803644,0.00001635819,0.0000054518073,0.000006644426,0.00054759305,0.000018546973,0.00081554404],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.99985015,0.00001960493,0.0000146237835,0.00005338048,0.00003551901,0.000026661786],"domain_scores_gemma":[0.99965763,0.000083031075,0.00011664053,0.000039633615,0.000041185333,0.000061806815],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00013253279,0.00016745145,0.00024014938,0.0007170823,0.00011264238,0.00025781043,0.0002105656,0.00010465899,0.00090583484],"category_scores_gemma":[0.0002697681,0.00012378277,0.00019889048,0.0002970245,0.0001874618,0.00015954289,0.00036430848,0.00019535367,0.00022249314],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00032121438,0.000009776404,0.041472834,0.00014220658,0.00005086544,0.00029125076,0.00010808648,0.0001568455,0.94172823,0.00051426835,0.000039981554,0.01516456],"study_design_scores_gemma":[0.000015781297,0.00040202975,0.7913983,0.000028144048,0.0000929939,0.0019188254,0.00014869767,0.0011755524,0.20026715,0.0005873776,0.003938485,0.000026669228],"about_ca_topic_score_codex":0.00069721637,"about_ca_topic_score_gemma":0.00092761207,"teacher_disagreement_score":0.00090583484,"about_ca_system_score_codex":0.00014432729,"about_ca_system_score_gemma":0.00013015252,"threshold_uncertainty_score":0.0030303597},"labels":[],"label_agreement":null},{"id":"W4281258467","doi":"10.1002/ajmg.a.62782","title":"A 79‐kb paternally inherited 7q32.2 microdeletion involving <scp><i>MEST</i></scp> in a patient with a <scp>Silver‐Russell</scp> syndrome‐like phenotype","year":2022,"lang":"en","type":"article","venue":"American Journal of Medical Genetics Part A","topic":"Genetic Syndromes and Imprinting","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":"University of Toronto; Children's Hospital of Eastern Ontario; Hospital for Sick Children; University of Ottawa","funders":"","keywords":"Phenotype; Genetics; Genomic imprinting; Uniparental disomy; Biology; Imprinting (psychology); Gene; Chromosome; DNA methylation; Karyotype; Gene expression","score_opus":0.007081262859299045,"score_gpt":0.2201342164133504,"score_spread":0.21305295355405135,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4281258467","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9961242,0.0003202738,0.0012977388,0.0005143547,0.000049969552,0.000026359416,0.0002248035,0.000078434095,0.0013638104],"genre_scores_gemma":[0.9978352,0.00014185152,0.00087025954,0.0001306851,0.000041588297,0.000009181933,0.00012586851,0.0000169433,0.00082836836],"study_design_codex":"case_report","study_design_gemma":"case_report","domain_scores_codex":[0.99983466,0.000014419938,0.000010870176,0.000069934154,0.000037641614,0.00003246309],"domain_scores_gemma":[0.9996941,0.00009666319,0.00006619178,0.0000126462055,0.000012816184,0.0001175529],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0000811318,0.0008300783,0.00043947832,0.0006733689,0.00052040094,0.00032965234,0.0004332522,0.0014298563,0.0016770101],"category_scores_gemma":[0.0006188629,0.00042790425,0.0003643227,0.00039113988,0.00064712623,0.000359023,0.00042961616,0.00091752625,0.00044402195],"study_design_candidate":"case_report","study_design_consensus":"case_report","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00019176623,0.00008343131,0.028079748,0.000058110618,0.000032037085,0.8651154,0.0007309912,0.00036647008,0.0986066,0.0004441087,0.00059631164,0.005695064],"study_design_scores_gemma":[0.000057004447,0.00048958126,0.08353936,0.000011626373,0.000062383035,0.8946636,0.00018401524,0.0009498105,0.018362056,0.00029464698,0.001348944,0.00003702444],"about_ca_topic_score_codex":0.0015110528,"about_ca_topic_score_gemma":0.0020269242,"teacher_disagreement_score":0.0016770101,"about_ca_system_score_codex":0.00034849576,"about_ca_system_score_gemma":0.00027947113,"threshold_uncertainty_score":0.005610168},"labels":[],"label_agreement":null},{"id":"W4281559669","doi":"10.1101/2022.05.24.493320","title":"Parent-of-origin detection and chromosome-scale haplotyping using long-read DNA methylation sequencing and Strand-seq","year":2022,"lang":"en","type":"preprint","venue":"bioRxiv (Cold Spring Harbor Laboratory)","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","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":"Canada's Michael Smith Genome Sciences Centre; University of British Columbia; BC Cancer Agency","funders":"Canadian Institutes of Health Research; Terry Fox Research Institute; University of British Columbia; Canada Research Chairs","keywords":"Autosome; Genetics; Biology; Haplotype; DNA methylation; DNA sequencing; Indel; Allele; Chromosome; DNA; Gene; Genotype; Single-nucleotide polymorphism","score_opus":0.023002636170163467,"score_gpt":0.2474176973530804,"score_spread":0.22441506118291693,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4281559669","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.67220145,0.0007110957,0.31102788,0.0001957635,0.000121630575,0.00021058874,0.010034525,0.002625539,0.0028714743],"genre_scores_gemma":[0.70226914,0.00030253295,0.28892773,0.00019478491,0.000024192745,0.00018183725,0.0045511522,0.0004975781,0.0030510367],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9995621,0.000067988905,0.000029283916,0.00016726425,0.00013763546,0.000035755784],"domain_scores_gemma":[0.9993362,0.00024636154,0.00014342867,0.00012566139,0.00008678532,0.00006155908],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00077336206,0.00035661214,0.0003490314,0.00056594657,0.0002713359,0.00043798712,0.00036160316,0.00048088658,0.0015279577],"category_scores_gemma":[0.0010267074,0.0003093138,0.00033522514,0.0003125473,0.0003121512,0.00023596319,0.0006110723,0.00063028606,0.0006860688],"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":[0.00008228995,0.00001488294,0.008749702,0.00005776023,0.00004184331,0.000071082955,0.00006903138,0.0009773787,0.98019505,0.0003726094,0.00021497234,0.00915352],"study_design_scores_gemma":[0.000018614564,0.00008444052,0.03887379,0.00001851549,0.000046080146,0.00051064824,0.00006629949,0.030273948,0.92295635,0.001232652,0.0058748634,0.000043807086],"about_ca_topic_score_codex":0.0013998075,"about_ca_topic_score_gemma":0.0045442474,"teacher_disagreement_score":0.0015279577,"about_ca_system_score_codex":0.000306827,"about_ca_system_score_gemma":0.00029446487,"threshold_uncertainty_score":0.005111575},"labels":[],"label_agreement":null},{"id":"W4281695503","doi":"10.1042/bsr20220610","title":"Proteins and proteases of Prader–Willi syndrome: a comprehensive review and perspectives","year":2022,"lang":"en","type":"review","venue":"Bioscience Reports","topic":"Genetic Syndromes and Imprinting","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":"Ottawa Hospital; SickKids Foundation; University of Ottawa; Hospital for Sick Children; University of Toronto","funders":"Foundation for Prader-Willi Research","keywords":"Hypotonia; Short stature; Disease; Bioinformatics; Genomic imprinting; Imprinting (psychology); Medicine; Biology; Genetics; Internal medicine; DNA methylation; Gene","score_opus":0.0536649125002168,"score_gpt":0.3146451358547597,"score_spread":0.2609802233545429,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4281695503","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":[0.00019411226,0.99907684,0.000073922616,0.00019826177,0.000136841,0.0000025181755,0.000020653557,0.0000055776923,0.0002911706],"genre_scores_gemma":[0.000635142,0.99851054,0.00016373374,0.0001590181,0.00026059538,0.0000046106975,0.000058032012,0.0000013094063,0.00020693266],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.99978405,0.00003300621,0.00005732527,0.00004277868,0.000058045884,0.000024849898],"domain_scores_gemma":[0.99958366,0.00020107455,0.00008507466,0.000008949648,0.000081973725,0.000039260332],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0005203025,0.0011335836,0.0015754902,0.0037011432,0.0003254777,0.0013070287,0.0008325204,0.0010797895,0.0028874525],"category_scores_gemma":[0.0007806155,0.00032835317,0.00080911146,0.0030570435,0.00040553958,0.0016855733,0.0007068736,0.0015577066,0.0010973649],"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":[0.00024520486,0.00016206526,0.0012849347,0.042587947,0.0003098437,0.0013826514,0.00023772188,0.00052081834,0.003650395,0.0029668969,0.05355533,0.8930962],"study_design_scores_gemma":[0.000023211176,0.00018929195,0.003131648,0.0080372235,0.00046782347,0.007847465,0.00018009749,0.00015807626,0.0007272319,0.00144112,0.9777465,0.00005035167],"about_ca_topic_score_codex":0.0012083482,"about_ca_topic_score_gemma":0.0014006231,"teacher_disagreement_score":0.0037011432,"about_ca_system_score_codex":0.00055566663,"about_ca_system_score_gemma":0.0011946942,"threshold_uncertainty_score":0.009659529},"labels":[],"label_agreement":null},{"id":"W4282546381","doi":"10.1186/s13073-022-01064-4","title":"Gain and loss of TASK3 channel function and its regulation by novel variation cause KCNK9 imprinting syndrome","year":2022,"lang":"en","type":"article","venue":"Genome Medicine","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":22,"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 Children's Hospital","funders":"Center for Individualized Medicine, Mayo Clinic; Deutsche Forschungsgemeinschaft","keywords":"Loss function; Phenotype; Imprinting (psychology); Biology; Genetics; Genomic imprinting; Intellectual disability; Bioinformatics; Neuroscience; Gene; Computational biology; DNA methylation; Gene expression","score_opus":0.010608952852647662,"score_gpt":0.2157817611501218,"score_spread":0.20517280829747414,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4282546381","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99422234,0.00026314674,0.004605895,0.00007260474,0.00001013622,0.000008183869,0.00029486863,0.00007521707,0.00044757558],"genre_scores_gemma":[0.9976539,0.00017529416,0.0018547254,0.000022585486,0.0000059102003,0.0000051687175,0.00013320489,0.000022366212,0.00012689848],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9998784,0.000015392203,0.0000145829445,0.000038382343,0.00003763526,0.00001565326],"domain_scores_gemma":[0.99978954,0.000090371854,0.000072587514,0.000016793108,0.000009095163,0.000021725888],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.000109404944,0.000560908,0.00022293036,0.00031594647,0.00015277941,0.00018249011,0.00024810657,0.00035135486,0.0017876958],"category_scores_gemma":[0.0005102511,0.00011930277,0.00040805887,0.0003123489,0.00042478254,0.00014368822,0.00031578474,0.00037513682,0.00024477925],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00088162656,0.000073942465,0.13634916,0.0002482574,0.00029062785,0.047193572,0.00048640868,0.0090355,0.7725994,0.0021218597,0.00059015275,0.030129481],"study_design_scores_gemma":[0.00013249616,0.00043959488,0.49275628,0.00010235327,0.0005545924,0.14242421,0.00047002692,0.025634607,0.32757673,0.004074424,0.00572805,0.0001066124],"about_ca_topic_score_codex":0.0008725617,"about_ca_topic_score_gemma":0.0011980993,"teacher_disagreement_score":0.0017876958,"about_ca_system_score_codex":0.00022672905,"about_ca_system_score_gemma":0.00019927222,"threshold_uncertainty_score":0.005980432},"labels":[],"label_agreement":null},{"id":"W4282842119","doi":"10.1002/mrd.23621","title":"IGF2R, KCNQ1, PLAGL1, and SNRPN DNA methylation is completed in bovine by the early antral follicle stage","year":2022,"lang":"en","type":"article","venue":"Molecular Reproduction and Development","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":5,"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","funders":"Natural Sciences and Engineering Research Council of Canada","keywords":"Biology; Antral follicle; Methylation; DNA methylation; Follicle; Genetics; Andrology; DNA; Molecular biology; Endocrinology; Gene; Ovary","score_opus":0.012465995144153839,"score_gpt":0.22961667399872293,"score_spread":0.2171506788545691,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4282842119","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9946268,0.0021759083,0.0012915913,0.000032472504,0.00000595578,0.0000032783746,0.0004952389,0.000034037126,0.0013347339],"genre_scores_gemma":[0.9969934,0.00056368485,0.00072218437,0.000021590504,0.0000027374845,0.0000048233583,0.0005077186,0.000012904505,0.0011709305],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9998876,0.000015040716,0.000006763638,0.000047940404,0.000020319136,0.000022411668],"domain_scores_gemma":[0.9998914,0.000026104974,0.000041163894,0.0000091715065,0.0000109730045,0.000021266753],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00010550963,0.000117307296,0.00013261838,0.00044324933,0.00014845876,0.0002063595,0.000113538525,0.00016474545,0.0012751573],"category_scores_gemma":[0.00020950363,0.00013412067,0.00008309444,0.00016068625,0.0001745658,0.00010563345,0.00009383498,0.0001356599,0.00024336972],"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":[0.0002707586,0.000006371338,0.01370251,0.000040040322,0.000010111757,0.00015304006,0.000118921016,0.00006101584,0.9811056,0.00010643595,0.00005679085,0.0043684747],"study_design_scores_gemma":[0.000021008902,0.0002720493,0.73183256,0.000024919536,0.000048961196,0.0020152377,0.0001672646,0.00063064526,0.25872877,0.0002634533,0.0059843375,0.000010891129],"about_ca_topic_score_codex":0.0056977132,"about_ca_topic_score_gemma":0.0075679277,"teacher_disagreement_score":0.0056977132,"about_ca_system_score_codex":0.0003138001,"about_ca_system_score_gemma":0.00011818825,"threshold_uncertainty_score":0.011329114},"labels":[],"label_agreement":null},{"id":"W4283726389","doi":"10.1016/j.jbiomech.2022.111213","title":"Lower extremity coordination and joint kinetic distribution during gait in adults with and without Prader-Willi Syndrome","year":2022,"lang":"en","type":"article","venue":"Journal of Biomechanics","topic":"Genetic Syndromes and Imprinting","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":"California State University, Fullerton; California State University","keywords":"Ankle; Gait; Medicine; Biomechanics; Physical medicine and rehabilitation; Obesity; Gait analysis; Physical therapy; Anatomy; Internal medicine","score_opus":0.006387930685537412,"score_gpt":0.20440844168734199,"score_spread":0.19802051100180457,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4283726389","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9996823,0.000038261973,0.000021745696,0.000007826382,0.0000015354873,0.0000022972401,0.000101711215,0.000001307194,0.00014301797],"genre_scores_gemma":[0.9995784,0.000030885796,0.000031883366,0.000010191934,0.0000031965308,0.0000037043715,0.00016916043,0.0000012823656,0.00017123966],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9998216,0.000024363666,0.000031455977,0.000056388664,0.000028141454,0.000038074115],"domain_scores_gemma":[0.99967587,0.00005479082,0.00012302413,0.0000146312495,0.000044136345,0.00008759474],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00016345209,0.00028668265,0.0003972949,0.0008586146,0.00023087976,0.0003312205,0.00016518873,0.00030508413,0.0011432737],"category_scores_gemma":[0.0011750236,0.00016051384,0.0001886123,0.0004746941,0.0002466647,0.00029087297,0.00037893854,0.0002177646,0.00019192017],"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":[0.0006982416,0.00009811544,0.9902503,0.00001786525,0.000063508014,0.00073424436,0.00048320484,0.00010421658,0.0042748423,0.000019102967,0.000075516524,0.003180878],"study_design_scores_gemma":[0.00000441358,0.000119678654,0.9992674,0.0000011717418,0.0000070715564,0.0003600051,0.000119551245,0.000051256047,0.000039767096,0.0000051329253,0.000023268149,0.0000013589008],"about_ca_topic_score_codex":0.00466644,"about_ca_topic_score_gemma":0.0063286126,"teacher_disagreement_score":0.00466644,"about_ca_system_score_codex":0.00016413505,"about_ca_system_score_gemma":0.00010272087,"threshold_uncertainty_score":0.009278595},"labels":[],"label_agreement":null},{"id":"W4283735939","doi":"10.1136/jmedgenet-2021-108288","title":"A 132 bp deletion affecting the <i>KCNQ1OT1</i> gene associated with Silver-Russell syndrome clinical phenotype","year":2022,"lang":"en","type":"article","venue":"Journal of Medical Genetics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":5,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Dalhousie University; Nova Scotia Health Authority; Izaak Walton Killam Health Centre; Vitalité Health Network; Atlantic Cancer Research Institute; Université de Moncton","funders":"Fondation de la recherche en santé du Nouveau-Brunswick","keywords":"Genomic imprinting; Genetics; Proband; Biology; Phenotype; Gene; Imprinting (psychology); Copy-number variation; Epigenetics; X-inactivation; X chromosome; DNA methylation; Mutation; Gene expression; Genome","score_opus":0.017521788524396117,"score_gpt":0.2809629543558431,"score_spread":0.263441165831447,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4283735939","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99762434,0.0002297142,0.0006419984,0.00009145699,0.000013158739,0.00001510471,0.00014027492,0.00004593583,0.001197957],"genre_scores_gemma":[0.99873596,0.00008871773,0.0005502511,0.000042730695,0.000018907911,0.0000074940476,0.00012008145,0.000012433776,0.00042353955],"study_design_codex":"case_report","study_design_gemma":"observational","domain_scores_codex":[0.9998344,0.000018956473,0.00001856045,0.000061062005,0.000034020173,0.000032939763],"domain_scores_gemma":[0.99942183,0.000176947,0.00019367035,0.000021503847,0.000030105795,0.00015592524],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.000098261466,0.0010068095,0.00042823132,0.00067706,0.00030757146,0.00018829443,0.00039495833,0.0007289032,0.0021889606],"category_scores_gemma":[0.0007861306,0.000258156,0.00015924833,0.0005198692,0.0005809728,0.00023089827,0.000457249,0.00044598852,0.0004193138],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.000563223,0.00010304192,0.060670264,0.00018870646,0.00005245914,0.7588177,0.00064847595,0.00046421785,0.16876553,0.00033782472,0.00087176554,0.008516796],"study_design_scores_gemma":[0.000039928767,0.00030212034,0.11150024,0.00001871854,0.000060933886,0.87197083,0.00011228532,0.00034172906,0.014232067,0.00015978958,0.0012333872,0.00002790102],"about_ca_topic_score_codex":0.00094231335,"about_ca_topic_score_gemma":0.00089858467,"teacher_disagreement_score":0.0021889606,"about_ca_system_score_codex":0.00019946878,"about_ca_system_score_gemma":0.00020540057,"threshold_uncertainty_score":0.0073227882},"labels":[],"label_agreement":null},{"id":"W4283805795","doi":"10.7554/elife.77898","title":"Genome-wide detection of imprinted differentially methylated regions using nanopore sequencing","year":2022,"lang":"en","type":"article","venue":"eLife","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","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":"Canada's Michael Smith Genome Sciences Centre; University of British Columbia; BC Cancer Agency","funders":"University of British Columbia Graduate School; Canada Research Chairs","keywords":"Differentially methylated regions; Genomic imprinting; Biology; DNA methylation; Imprinting (psychology); Nanopore sequencing; Bisulfite sequencing; Genome; Illumina Methylation Assay; Genetics; Computational biology; Germline; Epigenetics; CpG site; Genomics; DNA sequencing; Methylation; Gene; Gene expression","score_opus":0.019000132591906076,"score_gpt":0.24200954668157332,"score_spread":0.22300941408966724,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4283805795","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.8799815,0.0022151705,0.103934675,0.00015543522,0.00004285162,0.000107007094,0.0097392425,0.0009976532,0.0028264518],"genre_scores_gemma":[0.8602511,0.0009736135,0.12774575,0.0003060816,0.000020103656,0.00018615866,0.008493232,0.00010257398,0.0019213584],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9996797,0.00003717355,0.000014649876,0.00015344968,0.000082879975,0.000032267573],"domain_scores_gemma":[0.99972945,0.00010550538,0.000057520923,0.000038235397,0.000040753024,0.000028456001],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00031409552,0.00028039725,0.00028553972,0.00056161336,0.00018028019,0.000300315,0.0003209402,0.00043857392,0.00063610607],"category_scores_gemma":[0.00052156346,0.00018501058,0.00030713488,0.0003466151,0.00018310486,0.00018489665,0.00038945943,0.00042115635,0.00023692672],"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":[0.00006886314,0.000013093196,0.005116889,0.000057454185,0.000054213713,0.000045742214,0.00003889332,0.00050571526,0.98748094,0.00015354539,0.00012861931,0.0063359654],"study_design_scores_gemma":[0.000023709934,0.00021876315,0.10222217,0.00002049702,0.00015292503,0.0005459308,0.000070104645,0.01815247,0.86937195,0.0008334873,0.008351363,0.000036635043],"about_ca_topic_score_codex":0.00091397774,"about_ca_topic_score_gemma":0.0027995396,"teacher_disagreement_score":0.00091397774,"about_ca_system_score_codex":0.00019608502,"about_ca_system_score_gemma":0.0001368033,"threshold_uncertainty_score":0.0021279454},"labels":[],"label_agreement":null},{"id":"W4285188752","doi":"10.1007/978-1-0716-2533-0_18","title":"Tools and Techniques for Genomic Imprinting","year":2022,"lang":"en","type":"book-chapter","venue":"Springer protocols handbooks/Springer protocols","topic":"Genetic Syndromes and Imprinting","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":"Dalhousie University","funders":"","keywords":"Genomic imprinting; Imprinting (psychology); Computational biology; Biology; Genetics; Computer science; Evolutionary biology; Gene; DNA methylation","score_opus":0.036202625280582,"score_gpt":0.2978246800680739,"score_spread":0.2616220547874919,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4285188752","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":[0.0018130703,0.056903727,0.6315746,0.0024738647,0.0034453012,0.00027797665,0.0015308559,0.0076607247,0.2943199],"genre_scores_gemma":[0.020116426,0.0913339,0.40191716,0.0016886042,0.001150629,0.0010802429,0.003159369,0.0038208978,0.4757328],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.9992155,0.00008680017,0.00004498862,0.00010929176,0.00048542026,0.00005800341],"domain_scores_gemma":[0.9995552,0.00019036213,0.000019523479,0.00015057922,0.000059663445,0.000024611385],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0008546338,0.0015681568,0.0009634207,0.002557178,0.001104305,0.0027847334,0.0016911332,0.0012379256,0.040789615],"category_scores_gemma":[0.0013080157,0.001486987,0.00068866875,0.0032359,0.0018401694,0.0043239635,0.0029304412,0.004611835,0.038503017],"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":[0.00003465593,0.000050812385,0.00006323619,0.0008709613,0.000018210218,0.00029593272,0.00038201717,0.0010932478,0.04331717,0.30461645,0.109142534,0.54011476],"study_design_scores_gemma":[0.000005248909,0.000015016743,0.000063627995,0.00010742781,0.000008498916,0.0003887182,0.00003920994,0.00069287,0.022083588,0.06756847,0.90900034,0.000026987716],"about_ca_topic_score_codex":0.00066837965,"about_ca_topic_score_gemma":0.0012221553,"teacher_disagreement_score":0.040789615,"about_ca_system_score_codex":0.001019245,"about_ca_system_score_gemma":0.0008590582,"threshold_uncertainty_score":0.13645482},"labels":[],"label_agreement":null},{"id":"W4295876078","doi":"10.1101/2022.09.09.507324","title":"The imprinted <i>Mir483</i> is a growth suppressor and metabolic regulator functioning through IGF1","year":2022,"lang":"en","type":"preprint","venue":"bioRxiv (Cold Spring Harbor Laboratory)","topic":"Genetic Syndromes and Imprinting","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":"Montreal Clinical Research Institute","funders":"Japan Society for the Promotion of Science; Cambridge Institute for Medical Research, University of Cambridge; Biotechnology and Biological Sciences Research Council; Medical Research Council; Directorate for Biological Sciences; Cancer Research UK; Anatomical Society; Francis Crick Institute; Uehara Memorial Foundation","keywords":"Genomic imprinting; Psychological repression; Biology; Transgene; microRNA; Imprinting (psychology); Regulator; Suppressor; Endocrinology; Growth factor; Gene expression; Gene; Cell biology; Phenotype; Promoter; Internal medicine; Genetics; Receptor; DNA methylation; Medicine","score_opus":0.009018086399011983,"score_gpt":0.21248517553880977,"score_spread":0.2034670891397978,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4295876078","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.97034013,0.0010839496,0.020403914,0.00034539902,0.00009108157,0.00001728521,0.0012058847,0.00073871017,0.0057737445],"genre_scores_gemma":[0.9898337,0.0003108034,0.0044641895,0.00005290532,0.000014548396,0.000013638518,0.0005546014,0.00009983287,0.0046558217],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9999434,0.000007160389,0.000003335729,0.000016189457,0.000019241634,0.000010756124],"domain_scores_gemma":[0.99994814,0.0000064925007,0.000023682742,0.00000490718,0.0000032226578,0.00001347351],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00006928847,0.00028655148,0.00011607795,0.00019625244,0.00016016798,0.0002366621,0.00015691067,0.00022091347,0.0018086013],"category_scores_gemma":[0.00007644666,0.0000996477,0.00016299683,0.00008771436,0.00028380624,0.00008868173,0.00019399403,0.00032341582,0.00063006807],"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":[0.00006691411,0.000003976269,0.00065795425,0.0000133132535,0.0000032918847,0.00020634892,0.000007166376,0.00005608067,0.99658114,0.00037101863,0.00010778774,0.001925013],"study_design_scores_gemma":[0.000012065548,0.000054649954,0.007583044,0.0000046784917,0.00001063708,0.0018967945,0.000015150148,0.0011952447,0.9816742,0.0002783515,0.0072709727,0.000004222286],"about_ca_topic_score_codex":0.00038762315,"about_ca_topic_score_gemma":0.00037129232,"teacher_disagreement_score":0.0018086013,"about_ca_system_score_codex":0.000198621,"about_ca_system_score_gemma":0.00012791643,"threshold_uncertainty_score":0.006050408},"labels":[],"label_agreement":null},{"id":"W4296588680","doi":"10.3390/ijms231810580","title":"Preserved Sleep for the Same Level of Respiratory Disturbance in Children with Prader-Willi Syndrome","year":2022,"lang":"en","type":"article","venue":"International Journal of Molecular Sciences","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","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":"Stollery Children's Hospital; Women and Children’s Health Research Institute; University of Alberta","funders":"","keywords":"Respiratory disturbance index; Polysomnography; Medicine; Respiratory system; Body mass index; Sleep disorder; Apnea; Internal medicine; Oxygen saturation; Obstructive sleep apnea; Sleep apnea; Pediatrics; Insomnia; Oxygen","score_opus":0.035198408290163324,"score_gpt":0.28358443421939183,"score_spread":0.2483860259292285,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4296588680","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9992729,0.00042480772,0.000058557336,0.000022535058,0.000005690777,0.0000028323,0.0000452977,0.0000031349593,0.00016426883],"genre_scores_gemma":[0.99960214,0.00017138962,0.00009454127,0.000015451331,0.000008306943,0.0000026279752,0.000077403194,0.0000015579715,0.000026626489],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9996896,0.00006704176,0.000037846858,0.00009541468,0.00006819461,0.000041960546],"domain_scores_gemma":[0.9992353,0.0001401031,0.00040381198,0.000057270972,0.000048418333,0.00011517381],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0003452833,0.00023521521,0.0003073276,0.00054955354,0.00025302632,0.00032474624,0.0002083077,0.00025394326,0.0005978534],"category_scores_gemma":[0.0012946251,0.0001485583,0.00030083713,0.00036552065,0.0005180708,0.00032268622,0.0003071501,0.00040315627,0.00009897645],"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":[0.000121431476,0.000010805372,0.99491715,0.000020421505,0.000036900437,0.0007782279,0.00007155792,0.000026107127,0.0014580799,0.000028437293,0.00003905153,0.002491909],"study_design_scores_gemma":[0.0000040375244,0.00014015606,0.9964407,0.0000049490013,0.000017126591,0.003018535,0.000094585135,0.000030117011,0.00016552246,0.0000125381985,0.000069697024,0.0000019719814],"about_ca_topic_score_codex":0.0014984459,"about_ca_topic_score_gemma":0.0022904193,"teacher_disagreement_score":0.0014984459,"about_ca_system_score_codex":0.00021549815,"about_ca_system_score_gemma":0.00025053907,"threshold_uncertainty_score":0.0029794574},"labels":[],"label_agreement":null},{"id":"W4297199830","doi":"10.1016/j.omtm.2022.09.012","title":"Hypothalamic AAV-BDNF gene therapy improves metabolic function and behavior in the Magel2-null mouse model of Prader-Willi syndrome","year":2022,"lang":"en","type":"article","venue":"Molecular Therapy — Methods & Clinical Development","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":20,"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":"National Institute of Neurological Disorders and Stroke; National Cancer Institute","keywords":"Endocrinology; Internal medicine; Adipokine; Energy homeostasis; Leptin; Transgene; Neurotrophic factors; Genetic enhancement; Medicine; Adeno-associated virus; Obesity; Biology; Gene; Receptor; Vector (molecular biology)","score_opus":0.06070591502524848,"score_gpt":0.35561151785137285,"score_spread":0.2949056028261244,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4297199830","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9944036,0.00065909524,0.0032709537,0.00016681956,0.000040712504,0.00004617988,0.00031239292,0.00021018401,0.0008901164],"genre_scores_gemma":[0.98488104,0.0013136073,0.007623256,0.000089357534,0.000026320418,0.00012055349,0.00053456455,0.00006508479,0.0053461883],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9998247,0.000031558655,0.000021660677,0.00004225746,0.00004932188,0.000030500167],"domain_scores_gemma":[0.99986196,0.000013489652,0.00004947598,0.000013427788,0.000009438911,0.000052221978],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00020261454,0.0006513908,0.00034707817,0.00054904807,0.00012348038,0.00022816814,0.00028323993,0.00039858773,0.0012039543],"category_scores_gemma":[0.00013903501,0.00018335224,0.00024281577,0.00012587,0.0003814726,0.0002526394,0.00021661198,0.00078196236,0.00024890527],"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":[0.00027280854,0.00013431096,0.0001940067,0.000028467151,0.0000062370427,0.00010036697,0.000016333628,0.00008823512,0.996416,0.00011620364,0.000048411886,0.0025785835],"study_design_scores_gemma":[0.00018697792,0.0032275063,0.007473431,0.000026792482,0.000045530847,0.0010257546,0.000050439066,0.0022606053,0.98289263,0.00015045534,0.0026442287,0.000015629423],"about_ca_topic_score_codex":0.0005134135,"about_ca_topic_score_gemma":0.001133819,"teacher_disagreement_score":0.0012039543,"about_ca_system_score_codex":0.00022176585,"about_ca_system_score_gemma":0.00025137127,"threshold_uncertainty_score":0.004027605},"labels":[],"label_agreement":null},{"id":"W4308636364","doi":"10.1186/s13148-022-01358-9","title":"First step towards a consensus strategy for multi-locus diagnostic testing of imprinting disorders","year":2022,"lang":"en","type":"article","venue":"Clinical Epigenetics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":34,"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; Det Sundhedsvidenskabelige Fakultet, Københavns Universitet; Istituto Auxologico Italiano; Ministero dell'Università e della Ricerca; RWTH Aachen University; Gentofte Hospital; Instituto de Salud Carlos III; Rigshospitalet; University of Exeter; Faculty of Health and Medical Sciences, University of Western Australia; Universität Hamburg; University Hospital Southampton NHS Foundation Trust; Diabetes UK; National Institute for Health and Care Research; Wellcome Trust; Japan Agency for Medical Research and Development","keywords":"Imprinting (psychology); Locus (genetics); Human genetics; Genomic imprinting; Diagnostic test; Medicine; Genetics; Biology; Pediatrics; Gene","score_opus":0.0947107233993399,"score_gpt":0.3618741946444731,"score_spread":0.26716347124513323,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4308636364","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":[0.008713652,0.024318533,0.69362277,0.24517314,0.008588559,0.0030350443,0.0004799777,0.0034411256,0.0126271285],"genre_scores_gemma":[0.03408998,0.005776622,0.917147,0.03239665,0.0043781595,0.0021933813,0.00089650153,0.00039728347,0.002724377],"study_design_codex":"design_other","study_design_gemma":"theoretical_or_conceptual","domain_scores_codex":[0.9065787,0.043774325,0.017184105,0.0070539326,0.022108607,0.0033003753],"domain_scores_gemma":[0.6231102,0.08044516,0.013912134,0.029262397,0.2248663,0.028403845],"candidate_categories":["metaresearch"],"consensus_categories":[],"category_scores_codex":[0.19092247,0.003158896,0.003984321,0.015869776,0.0037511666,0.011367554,0.016584855,0.014291947,0.0061876127],"category_scores_gemma":[0.16444327,0.0022074254,0.0036204003,0.005155909,0.00490772,0.011549578,0.017923025,0.022524565,0.006345566],"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":[0.00046939813,0.0013477319,0.030588528,0.004167268,0.0009316877,0.0055897906,0.0036488983,0.005564643,0.0069465134,0.021281812,0.19798777,0.7214761],"study_design_scores_gemma":[0.001088249,0.0027663934,0.04117974,0.021997003,0.0018319092,0.024011865,0.012112037,0.03859779,0.018725941,0.1810339,0.6553879,0.0012674575],"about_ca_topic_score_codex":0.0044380357,"about_ca_topic_score_gemma":0.0063888533,"teacher_disagreement_score":0.19092247,"about_ca_system_score_codex":0.0074158423,"about_ca_system_score_gemma":0.03869413,"threshold_uncertainty_score":0.99773663},"labels":[],"label_agreement":null},{"id":"W4309899484","doi":"10.3389/fgene.2022.1041943","title":"Do the diverse phenotypes of Prader-Willi syndrome reflect extremes of covariation in typical populations?","year":2022,"lang":"en","type":"article","venue":"Frontiers in Genetics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":2,"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":"Common Fund; National Institute of Neurological Disorders and Stroke; National Human Genome Research Institute; National Heart, Lung, and Blood Institute; National Institute of Mental Health; Canadian Network for Research and Innovation in Machining Technology, Natural Sciences and Engineering Research Council of Canada; NIH Office of the Director; Natural Sciences and Engineering Research Council of Canada; National Cancer Institute; National Institutes of Health; National Institute on Drug Abuse; Simon Fraser University; University of Alberta","keywords":"Phenotype; Biology; Autism; Autism spectrum disorder; Mood; Cognition; Phenotypic trait; Genetics; Genomic imprinting; Psychology; Gene; Developmental psychology; Neuroscience; Clinical psychology; DNA methylation","score_opus":0.02794259510006615,"score_gpt":0.2690863082636271,"score_spread":0.24114371316356098,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4309899484","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9978523,0.00025537,0.001310456,0.000071029426,0.0000027134547,0.0000059337995,0.00017009233,0.000008742031,0.00032338614],"genre_scores_gemma":[0.99905866,0.00012691294,0.00060797826,0.000026686095,0.000007940807,0.000008140561,0.00011786028,0.0000046180176,0.000041045405],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9986425,0.00039612953,0.00013777518,0.00051416125,0.0002157845,0.0000936291],"domain_scores_gemma":[0.9980884,0.0006617935,0.0006799749,0.00034221855,0.00010572055,0.000121777884],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0009754075,0.00023217888,0.00049720117,0.0011415194,0.00032584596,0.00044281877,0.0004372669,0.00029440955,0.0010622947],"category_scores_gemma":[0.005181627,0.00022327773,0.00026705422,0.0009593917,0.0011449831,0.0005497707,0.0007920438,0.0002859448,0.00010626985],"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":[0.00017831242,0.000024406714,0.9631738,0.000047315454,0.00026559047,0.0010203514,0.0015185593,0.00019202604,0.014678775,0.0008042331,0.00012215153,0.017974438],"study_design_scores_gemma":[0.0000039825263,0.00006385706,0.9954116,0.0000060993257,0.000027567206,0.0021178783,0.00040190766,0.00015145056,0.0006114253,0.00092868286,0.0002652206,0.0000103246475],"about_ca_topic_score_codex":0.0012396773,"about_ca_topic_score_gemma":0.0024722726,"teacher_disagreement_score":0.0012396773,"about_ca_system_score_codex":0.00016090935,"about_ca_system_score_gemma":0.00024051513,"threshold_uncertainty_score":0.005158484},"labels":[],"label_agreement":null},{"id":"W4310262032","doi":"10.1177/00220345221132268","title":"Novel Genetic Determinants of Dental Maturation in Children","year":2022,"lang":"en","type":"review","venue":"Journal of Dental Research","topic":"Genetic Syndromes and Imprinting","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":"McGill University","funders":"National Institute of Arthritis and Musculoskeletal and Skin Diseases; Medical Research Council; University of Bristol; Erasmus Medisch Centrum; ZonMw; National Institutes of Health; Foundation for the National Institutes of Health; Cancer Research UK; Nederlandse Organisatie voor Wetenschappelijk Onderzoek; Wellcome Trust; Erasmus Universiteit Rotterdam; National Institute for Health and Care Research","keywords":"Genome-wide association study; Population stratification; Craniofacial; Population; Genetics; Allele; Genetic association; Medicine; Biology; Genotype; Gene; Single-nucleotide polymorphism","score_opus":0.07988921791753534,"score_gpt":0.41610109155240066,"score_spread":0.3362118736348653,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4310262032","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":[0.97358996,0.02114107,0.0012977886,0.000500302,0.00008581156,0.000026482194,0.0018843774,0.00004408615,0.0014301519],"genre_scores_gemma":[0.992687,0.0043354686,0.0012760782,0.00016552852,0.000073890755,0.000033853863,0.00093985203,0.000024773424,0.00046348615],"study_design_codex":"observational","study_design_gemma":"not_applicable","domain_scores_codex":[0.9988381,0.0002849003,0.00010570093,0.0004692115,0.00018785846,0.00011410916],"domain_scores_gemma":[0.9990852,0.00042852783,0.00027692455,0.000083065635,0.00006388036,0.000062477266],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0014548253,0.0007673922,0.0008102024,0.0009450156,0.0004765981,0.00092314504,0.0006698706,0.00092176686,0.0022130967],"category_scores_gemma":[0.0028850208,0.00067626196,0.002416105,0.0017819343,0.00046272043,0.00030264028,0.0007315947,0.0009420005,0.00015679895],"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":[0.0015589384,0.000059450245,0.96899736,0.0005185301,0.006077365,0.0014671781,0.0003261271,0.00058686844,0.004779762,0.00072478567,0.0012205701,0.013683099],"study_design_scores_gemma":[0.0001564517,0.00013165147,0.9908647,0.00015224534,0.0036984384,0.0010698021,0.00017512606,0.0006487276,0.0005100098,0.0005672428,0.0020070309,0.000018565135],"about_ca_topic_score_codex":0.008793723,"about_ca_topic_score_gemma":0.008388287,"teacher_disagreement_score":0.008793723,"about_ca_system_score_codex":0.00048385066,"about_ca_system_score_gemma":0.0005815255,"threshold_uncertainty_score":0.017485082},"labels":[],"label_agreement":null},{"id":"W4311093575","doi":"10.3390/ijms232315115","title":"Comparison of Body Composition, Muscle Strength and Cardiometabolic Profile in Children with Prader-Willi Syndrome and Non-Alcoholic Fatty Liver Disease: A Pilot Study","year":2022,"lang":"en","type":"article","venue":"International Journal of Molecular Sciences","topic":"Genetic Syndromes and Imprinting","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":"University of Alberta","funders":"","keywords":"Medicine; Internal medicine; Lean body mass; Endocrinology; Fatty liver; Anthropometry; Blood pressure; Body mass index; Lipid profile; Obesity; Disease; Diabetes mellitus; Body weight","score_opus":0.013275722476765062,"score_gpt":0.28248746350098497,"score_spread":0.2692117410242199,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4311093575","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99976593,0.000025294024,0.000031400992,0.0000058969504,0.0000019992804,0.000021627573,0.00009478545,0.0000013277828,0.000051672836],"genre_scores_gemma":[0.9990822,0.00005985515,0.00027822875,0.000025132624,0.000010308272,0.00006327368,0.00038885337,0.00000244589,0.00008969594],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.999263,0.00022489032,0.00008169446,0.00018334787,0.000115599236,0.0001314446],"domain_scores_gemma":[0.99851936,0.00032216552,0.00038941216,0.00013423133,0.00017627775,0.00045855506],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0010186611,0.0008456506,0.00075021427,0.00093972986,0.0005841408,0.00045272394,0.00042832806,0.00060012523,0.0010645235],"category_scores_gemma":[0.0019379589,0.00047199652,0.000858703,0.00073923403,0.000600111,0.000631158,0.00079114054,0.0007379671,0.00028578946],"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":[0.0011059006,0.0006712426,0.9944635,0.000024982202,0.00007362072,0.00054321985,0.00034302095,0.000038436774,0.0013161245,0.000011669793,0.00005647669,0.0013518066],"study_design_scores_gemma":[0.00007945084,0.0025542674,0.9957799,0.000003841422,0.000029879004,0.0008406745,0.0003922361,0.00006797443,0.00014466236,0.000006141303,0.00009587952,0.000005058322],"about_ca_topic_score_codex":0.005860372,"about_ca_topic_score_gemma":0.0050421744,"teacher_disagreement_score":0.005860372,"about_ca_system_score_codex":0.0004498357,"about_ca_system_score_gemma":0.0005572264,"threshold_uncertainty_score":0.01165247},"labels":[],"label_agreement":null},{"id":"W4313214635","doi":"10.1016/j.xgen.2022.100233","title":"Parent-of-origin detection and chromosome-scale haplotyping using long-read DNA methylation sequencing and Strand-seq","year":2022,"lang":"en","type":"article","venue":"Cell Genomics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","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":"Terry Fox Research Institute; Canada's Michael Smith Genome Sciences Centre; University of British Columbia","funders":"","keywords":"Autosome; Biology; Genetics; Haplotype; DNA methylation; Indel; DNA sequencing; Human genome; Allele; Chromosome; Genome; DNA; Gene; Genotype; Single-nucleotide polymorphism","score_opus":0.022737167996274805,"score_gpt":0.24062852284335023,"score_spread":0.21789135484707542,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4313214635","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.7207198,0.00076630374,0.2662858,0.00012695284,0.00009669178,0.00023160537,0.0070666345,0.0016586325,0.0030475052],"genre_scores_gemma":[0.73422134,0.00040757385,0.25663576,0.00021767142,0.000021675178,0.00023498817,0.004707266,0.00039992816,0.0031537425],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9995503,0.000053387375,0.000028427901,0.00020165391,0.00012786635,0.000038276474],"domain_scores_gemma":[0.9994099,0.00019360395,0.00013957449,0.00011089508,0.000090156034,0.000055727687],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0005551708,0.0003664229,0.000337453,0.00051228184,0.00031672302,0.00043738735,0.00037841726,0.0005162073,0.0013522904],"category_scores_gemma":[0.0009804729,0.0003017195,0.0003836548,0.00034776298,0.000301044,0.0002443106,0.00059641374,0.0005889935,0.00055836444],"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":[0.00007456752,0.0000131534425,0.008103126,0.00006308163,0.000044399007,0.000073343304,0.00009313619,0.00062681077,0.981399,0.00034916465,0.00013429145,0.009025955],"study_design_scores_gemma":[0.00001817313,0.000116756615,0.048360784,0.000022068103,0.000070839575,0.0006010222,0.00009134474,0.024652077,0.91823035,0.0010729579,0.0067147613,0.000048849968],"about_ca_topic_score_codex":0.0015409603,"about_ca_topic_score_gemma":0.006923826,"teacher_disagreement_score":0.0015409603,"about_ca_system_score_codex":0.00030178364,"about_ca_system_score_gemma":0.00031528957,"threshold_uncertainty_score":0.0045238137},"labels":[],"label_agreement":null},{"id":"W4315753440","doi":"10.1210/clinem/dgad015","title":"Intranasal Carbetocin Reduces Hyperphagia, Anxiousness, and Distress in Prader-Willi Syndrome: CARE-PWS Phase 3 Trial","year":2023,"lang":"en","type":"article","venue":"The Journal of Clinical Endocrinology & Metabolism","topic":"Genetic Syndromes and Imprinting","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":"University of British Columbia; University of Alberta; Hospital for Sick Children; University of Toronto; Centre Hospitalier Universitaire Sainte-Justine","funders":"","keywords":"Placebo; Medicine; Anxiety; Clinical endpoint; Context (archaeology); Distress; Randomized controlled trial; Internal medicine; Clinical trial; Psychiatry; Clinical psychology","score_opus":0.03399671080429532,"score_gpt":0.37521815995375923,"score_spread":0.3412214491494639,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4315753440","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9862244,0.0054517225,0.00043291977,0.00069364667,0.0002483144,0.0044137775,0.0010372921,0.0001069112,0.0013910007],"genre_scores_gemma":[0.9855274,0.0037747805,0.0014004222,0.001105742,0.0002766152,0.004973756,0.0012161926,0.000019206633,0.0017060055],"study_design_codex":"randomized_trial","study_design_gemma":"randomized_trial","domain_scores_codex":[0.99963534,0.00018765804,0.000022708582,0.000055402455,0.000043926622,0.000054831253],"domain_scores_gemma":[0.9992539,0.00018393819,0.00021965633,0.000048024616,0.000072040086,0.00022232273],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0012276582,0.0011018425,0.001722737,0.00032655406,0.00044233678,0.0006952487,0.00095795275,0.001508843,0.0047384826],"category_scores_gemma":[0.0016058908,0.00039384488,0.0016008461,0.0003343516,0.00085599325,0.0005867545,0.00033400496,0.0022428029,0.0004756595],"study_design_candidate":"randomized_trial","study_design_consensus":"randomized_trial","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.948984,0.0105415,0.001699798,0.0015625581,0.0011177007,0.00013527146,0.00008635612,0.00030047423,0.0062068966,0.00010364167,0.0015614072,0.027700378],"study_design_scores_gemma":[0.93991166,0.056213923,0.0026102231,0.000041700805,0.00025560017,0.000057106674,0.00001707151,0.00018609466,0.00032181502,0.00004878885,0.0003284539,0.0000076258866],"about_ca_topic_score_codex":0.0016937049,"about_ca_topic_score_gemma":0.0038658655,"teacher_disagreement_score":0.0047384826,"about_ca_system_score_codex":0.000773319,"about_ca_system_score_gemma":0.001275291,"threshold_uncertainty_score":0.015851796},"labels":[],"label_agreement":null},{"id":"W4319163406","doi":"10.1038/s41598-023-29248-x","title":"Noncanonical regulation of imprinted gene Igf2 by amyloid-beta 1–42 in Alzheimer’s disease","year":2023,"lang":"en","type":"article","venue":"Scientific Reports","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":14,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Dalhousie University","funders":"Dalhousie University; Natural Sciences and Engineering Research Council of Canada; Fondation Brain Canada","keywords":"Epigenetics; DNA methylation; Genomic imprinting; MECP2; Histone; Biology; Epigenomics; Insulin-like growth factor 2; Methylation; Gene expression; Endocrinology; Regulation of gene expression; Internal medicine; Gene; Genetics; Medicine; Phenotype","score_opus":0.015123925852903532,"score_gpt":0.2634072047206951,"score_spread":0.24828327886779158,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4319163406","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9919334,0.0023740695,0.0027403517,0.00015487241,0.000059140722,0.000005893103,0.0006932488,0.000067400106,0.0019717119],"genre_scores_gemma":[0.9956463,0.0009106611,0.00071442255,0.000047757043,0.000021507361,0.0000063888588,0.000251761,0.00001317324,0.0023880347],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9999542,0.000004866427,0.0000029849664,0.000015035551,0.000013953461,0.000008955587],"domain_scores_gemma":[0.99992824,0.000009382062,0.000028517683,0.00000657399,0.000009962733,0.000017358883],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.000070086244,0.00023655787,0.00010158933,0.0002080808,0.00008928376,0.00014605158,0.00010555985,0.00010098549,0.0018762633],"category_scores_gemma":[0.000089136665,0.000077911885,0.000111959496,0.0000982342,0.00018263058,0.000076696895,0.00013888911,0.00014094973,0.0002489428],"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":[0.00031212048,0.000016384916,0.0092703635,0.000032714266,0.000016814747,0.0006799994,0.000038777638,0.000056022593,0.9846001,0.00028099405,0.00020126604,0.004494467],"study_design_scores_gemma":[0.000042180673,0.00023559158,0.5237659,0.000016765085,0.000064264445,0.0045827795,0.00014823234,0.0009956828,0.46235836,0.0008409033,0.006933703,0.00001565797],"about_ca_topic_score_codex":0.0008837462,"about_ca_topic_score_gemma":0.0011362329,"teacher_disagreement_score":0.0018762633,"about_ca_system_score_codex":0.00014260934,"about_ca_system_score_gemma":0.00011633249,"threshold_uncertainty_score":0.0062767267},"labels":[],"label_agreement":null},{"id":"W4319321105","doi":"10.3389/fnins.2023.1126970","title":"Prader–Willi syndrome: Symptoms and topiramate response in light of genetics","year":2023,"lang":"en","type":"article","venue":"Frontiers in Neuroscience","topic":"Genetic Syndromes and Imprinting","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":"McGill University","funders":"","keywords":"Topiramate; Impulsivity; Medicine; Psychiatry; Pharmacogenetics; Uniparental disomy; Pediatrics; Psychology; Epilepsy; Genetics; Chromosome; Genotype; Biology; Karyotype","score_opus":0.008980407679292904,"score_gpt":0.23955489099761398,"score_spread":0.2305744833183211,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4319321105","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9970583,0.0010156538,0.00015667894,0.00009221139,0.000010691298,0.000032449538,0.0002531125,0.000007685846,0.0013732219],"genre_scores_gemma":[0.9988532,0.00036822207,0.0001633829,0.00004430452,0.000024647681,0.000010221788,0.00020070029,0.0000020444552,0.00033321785],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9997919,0.000033180208,0.000031818723,0.00005189335,0.00004948865,0.000041779396],"domain_scores_gemma":[0.9996166,0.000104803374,0.00012956145,0.000019285972,0.000029865481,0.0000998715],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00018495627,0.0003580236,0.00040302405,0.0010562193,0.00038893698,0.00026661792,0.0002641386,0.00037708497,0.0017426636],"category_scores_gemma":[0.0011347434,0.00013410648,0.0002450964,0.0006091798,0.00036491902,0.00032141633,0.00033788392,0.00039588983,0.00018250437],"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":[0.00042854482,0.00011641763,0.8680898,0.00008104281,0.00005739922,0.119020306,0.00040083766,0.00013045894,0.003625232,0.00016185972,0.0003631093,0.0075249257],"study_design_scores_gemma":[0.000028341508,0.00034677092,0.7396165,0.000025824418,0.00005024743,0.25764522,0.0003204095,0.0002474865,0.00056493253,0.00014374118,0.0009943598,0.000016171283],"about_ca_topic_score_codex":0.0018886926,"about_ca_topic_score_gemma":0.0019605453,"teacher_disagreement_score":0.0018886926,"about_ca_system_score_codex":0.00021005969,"about_ca_system_score_gemma":0.00034693873,"threshold_uncertainty_score":0.005829811},"labels":[],"label_agreement":null},{"id":"W4319736580","doi":"10.3920/978-90-8686-940-4_750","title":"750. Genome-wide association study for ectopic ureter in three dog breeds","year":2022,"lang":"en","type":"article","venue":"","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":0,"is_retracted":false,"has_abstract":true,"route_ca_aff":false,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":true,"ca_institutions":"","funders":"","keywords":"Labrador Retriever; Breed; Bonferroni correction; Veterinary medicine; Felis catus; Ectopic ureter; Biology; Medicine; Urinary system; Genetics; CATS; Anatomy; Internal medicine; Pathology","score_opus":0.011485576845644734,"score_gpt":0.2430181393045681,"score_spread":0.23153256245892334,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4319736580","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9987669,0.00023078165,0.00031030847,0.000033180288,0.000003401172,0.000004249377,0.0002611978,0.000007147301,0.00038276674],"genre_scores_gemma":[0.998793,0.000056948913,0.0003863739,0.000018743936,0.0000033901563,0.000006673542,0.0003655199,0.0000044663643,0.00036490758],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99915016,0.00021335616,0.00005743997,0.00032930955,0.0001436363,0.00010613098],"domain_scores_gemma":[0.99933726,0.00023443751,0.00018879418,0.00006864381,0.000059208764,0.00011158813],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00075854495,0.00018754188,0.00029525533,0.0009802352,0.00053635356,0.0004774978,0.000314818,0.00032754435,0.0022101505],"category_scores_gemma":[0.0009915673,0.00017153179,0.00048480704,0.00090399233,0.00037025756,0.000121419216,0.00030111402,0.00034943575,0.00013786941],"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":[0.00058299396,0.00004802489,0.98297125,0.000023227636,0.00035142343,0.00072428194,0.0002164704,0.00007871526,0.0108202435,0.00009918358,0.0001743286,0.00390992],"study_design_scores_gemma":[0.000011567046,0.000057289406,0.9985689,0.0000039136394,0.00010273782,0.00048775683,0.00007724852,0.00012835847,0.00024578624,0.000015154015,0.0002988867,0.00000230218],"about_ca_topic_score_codex":0.018304456,"about_ca_topic_score_gemma":0.03184902,"teacher_disagreement_score":0.018304456,"about_ca_system_score_codex":0.00038350635,"about_ca_system_score_gemma":0.000417983,"threshold_uncertainty_score":0.036395848},"labels":[],"label_agreement":null},{"id":"W4320001616","doi":"10.1016/b978-0-12-821785-6.00011-6","title":"Genomic imprinting and developmental physiology: intrauterine growth and postnatal period","year":2023,"lang":"en","type":"book-chapter","venue":"Elsevier eBooks","topic":"Genetic Syndromes and Imprinting","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":"Université de Montréal","funders":"Medical Research Council","keywords":"Genomic imprinting; Biology; Imprinting (psychology); Offspring; Period (music); Phenotype; In utero; Gene; Epigenetics; Gene expression; Placenta; Fetus; Genetics; Physiology; DNA methylation; Pregnancy","score_opus":0.00891226907335172,"score_gpt":0.20934734329443333,"score_spread":0.20043507422108162,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4320001616","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":[0.0040034275,0.4267339,0.0071476437,0.002060159,0.0015674388,0.000027006698,0.0005258784,0.00029397735,0.5576405],"genre_scores_gemma":[0.025144901,0.2373154,0.00418804,0.0006893104,0.00085699785,0.00008602606,0.00045575455,0.00013159758,0.73113203],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.99995184,0.000005893532,0.0000025568115,0.000011056423,0.000023446593,0.0000052326654],"domain_scores_gemma":[0.9999596,0.000021860571,0.0000029077048,0.000003477695,0.000006329154,0.000005855079],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00011500364,0.0006048036,0.00036948288,0.00058891403,0.00024858274,0.0011377069,0.0005350426,0.0006878574,0.024292976],"category_scores_gemma":[0.00018715853,0.00023209589,0.00013193047,0.00089617516,0.0005374782,0.001064991,0.0005617258,0.0010240269,0.008322486],"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":[0.00012320756,0.000046815134,0.00037046804,0.0004016188,0.000013364663,0.0005177357,0.00033451323,0.00062920846,0.015578561,0.06840626,0.071911134,0.8416671],"study_design_scores_gemma":[0.000006730779,0.000030994313,0.002156288,0.0002442653,0.000010227998,0.0006857657,0.0001423786,0.00012924698,0.0017355672,0.022002717,0.9728463,0.000009434702],"about_ca_topic_score_codex":0.0016341163,"about_ca_topic_score_gemma":0.0030916722,"teacher_disagreement_score":0.024292976,"about_ca_system_score_codex":0.00049920706,"about_ca_system_score_gemma":0.00044712998,"threshold_uncertainty_score":0.08126807},"labels":[],"label_agreement":null},{"id":"W4320484851","doi":"10.31542/r.2726","title":"It’s a burden but… having a sibling with Prader Willi syndrome: stress, growth, and perceived burden","year":2022,"lang":"en","type":"dissertation","venue":"","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":0,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"MacEwan University","funders":"MacEwan University","keywords":"Neurotypical; Sibling; Feeling; Psychology; Clinical psychology; Population; Sibling relationship; Developmental psychology; Medicine; Environmental health; Autism spectrum disorder; Social psychology","score_opus":0.007328141478877899,"score_gpt":0.23978635506320425,"score_spread":0.23245821358432636,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4320484851","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9897626,0.0014168704,0.00020188282,0.0024389648,0.000105965875,0.000022201912,0.00007009463,0.000003095219,0.0059783375],"genre_scores_gemma":[0.98709947,0.0038309325,0.00057969085,0.00045980245,0.000045020202,0.000026557333,0.000093198214,0.0000025434629,0.007862835],"study_design_codex":"observational","study_design_gemma":"qualitative","domain_scores_codex":[0.9998913,0.000031692987,0.0000049344803,0.000013586132,0.000040611012,0.00001794336],"domain_scores_gemma":[0.99986196,0.000027040935,0.000035639405,0.0000057138723,0.000022317825,0.00004737972],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00031995188,0.000107396874,0.000115659204,0.000110485635,0.00037991386,0.00041001925,0.00006848612,0.00015680717,0.0028755015],"category_scores_gemma":[0.00069347624,0.00005849998,0.00009993422,0.00013604983,0.0002679241,0.0002677418,0.00025930826,0.0004547518,0.00025011663],"study_design_candidate":"qualitative","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00038981327,0.0012711927,0.5128886,0.00054968963,0.00012451757,0.0063798423,0.062340625,0.00012703233,0.025910646,0.0040541454,0.02123789,0.36472598],"study_design_scores_gemma":[0.000031605254,0.0007767643,0.907126,0.00037586124,0.000052759053,0.00561505,0.055708595,0.000105888816,0.0019239463,0.001627702,0.026628561,0.0000272124],"about_ca_topic_score_codex":0.001764431,"about_ca_topic_score_gemma":0.0041029677,"teacher_disagreement_score":0.0028755015,"about_ca_system_score_codex":0.00024124637,"about_ca_system_score_gemma":0.00036396983,"threshold_uncertainty_score":0.009619534},"labels":[],"label_agreement":null},{"id":"W4321499146","doi":"10.1111/ijpo.13006","title":"Incorporation of patient and family values and preferences for health‐related outcomes in paediatric obesity management: A systematic review","year":2023,"lang":"en","type":"review","venue":"Pediatric Obesity","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","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":"Lakehead University; University of Calgary; University of Alberta; Trillium Health Centre","funders":"Obesity Canada; Canadian Institutes of Health Research; Alberta Innovates","keywords":"Medicine; Psychological intervention; CINAHL; MEDLINE; Scopus; PsycINFO; Overweight; Systematic review; Obesity; Family medicine; Clinical psychology; Psychiatry","score_opus":0.022933263316062918,"score_gpt":0.2934605941422216,"score_spread":0.27052733082615865,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4321499146","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":[0.0036741174,0.9937338,0.00029672077,0.0004690452,0.00010832183,0.00071772357,0.00046572695,0.0000070910883,0.0005274032],"genre_scores_gemma":[0.06737147,0.927863,0.0018864273,0.00068662444,0.000092712515,0.0017074922,0.00026036755,0.000006591267,0.00012529845],"study_design_codex":"systematic_review","study_design_gemma":"systematic_review","domain_scores_codex":[0.97542614,0.012573624,0.007284478,0.0010135124,0.0033558486,0.00034640756],"domain_scores_gemma":[0.9157908,0.0659474,0.0130414255,0.0009722701,0.0037663698,0.00048174258],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.021159766,0.0011011683,0.006225961,0.010047957,0.0006842793,0.0035076493,0.0014743557,0.0016786715,0.0035967047],"category_scores_gemma":[0.09433316,0.0009807966,0.00717728,0.01041793,0.0011972295,0.00357619,0.0017521756,0.0016033165,0.00019541458],"study_design_candidate":"systematic_review","study_design_consensus":"systematic_review","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00023842457,0.000027774155,0.0017979562,0.9370222,0.009042503,0.00007725903,0.00072228303,0.00008189048,0.000066703724,0.00030466975,0.0007169056,0.049901374],"study_design_scores_gemma":[0.00022099869,0.0001748787,0.004671052,0.9544405,0.032128137,0.00026919774,0.00076273235,0.00007748644,0.00009649894,0.0002701068,0.006850485,0.000037863516],"about_ca_topic_score_codex":0.006215216,"about_ca_topic_score_gemma":0.017634746,"teacher_disagreement_score":0.021159766,"about_ca_system_score_codex":0.0043681934,"about_ca_system_score_gemma":0.014352921,"threshold_uncertainty_score":0.11190486},"labels":[],"label_agreement":null},{"id":"W4321748330","doi":"10.1002/jbmr.4795","title":"Rare and Common Variants in GALNT3 May Affect Bone Mass Independently of Phosphate Metabolism","year":2020,"lang":"en","type":"article","venue":"Journal of Bone and Mineral Research","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","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":"Health Care Foundation","funders":"National Health and Medical Research Council; Seventh Framework Programme; Elizabeth Blackwell Institute for Health Research, University of Bristol; Menzies Institute for Medical Research; Medical Research Council; International Seafood Sustainability Foundation; Versus Arthritis; Australian Cancer Research Foundation; Medical Research Council Canada; University of Tasmania; University of Bristol; University of New South Wales; Wellcome Trust","keywords":"Osteoporosis; Femoral neck; Genetics; Exome sequencing; Biology; Bone mineral; Endocrinology; Internal medicine; Medicine; Gene; Phenotype","score_opus":0.036031992470024955,"score_gpt":0.3250637518560142,"score_spread":0.28903175938598924,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4321748330","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9896488,0.0041281045,0.002108368,0.00052350457,0.00004380271,0.00001621215,0.0013552252,0.00011432042,0.0020616578],"genre_scores_gemma":[0.9976241,0.0006100712,0.0007382597,0.00015490231,0.000046611214,0.0000072201915,0.00035147354,0.00001953721,0.0004478991],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.999793,0.000033508415,0.00002634916,0.00006934833,0.00005532628,0.000022538103],"domain_scores_gemma":[0.99967515,0.00012396151,0.00012959908,0.00002097614,0.00001602503,0.00003427147],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00019556837,0.0008753092,0.00046619945,0.00054001826,0.00025899892,0.00040253357,0.00032365578,0.0008349534,0.0035793178],"category_scores_gemma":[0.0008001263,0.00014233112,0.00066160096,0.0008979231,0.00045058524,0.00017690261,0.00031956745,0.0004335821,0.00029988555],"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":[0.0048815166,0.00016093336,0.5576378,0.00077844923,0.001846064,0.07380807,0.0006517745,0.0023425035,0.2860899,0.0035176715,0.0027371,0.06554816],"study_design_scores_gemma":[0.00025961877,0.00035837232,0.86490965,0.00020943879,0.00086961186,0.09924271,0.00019791727,0.0027785162,0.018036116,0.004169011,0.008908771,0.0000602941],"about_ca_topic_score_codex":0.0018796703,"about_ca_topic_score_gemma":0.0022821787,"teacher_disagreement_score":0.0035793178,"about_ca_system_score_codex":0.00025157843,"about_ca_system_score_gemma":0.00014593102,"threshold_uncertainty_score":0.011974037},"labels":[],"label_agreement":null},{"id":"W4324156277","doi":"10.1186/s13059-023-02869-1","title":"Conservation and divergence of canonical and non-canonical imprinting in murids","year":2023,"lang":"en","type":"review","venue":"Genome biology","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":25,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"BC Children's Hospital; University of British Columbia","funders":"Institute of Genetics; National Institute for Physiological Sciences; Japan Society for the Promotion of Science; Natural Sciences and Engineering Research Council of Canada; Canadian Institutes of Health Research; Fondation ARC pour la Recherche sur le Cancer; Provincial Health Services Authority; Fondation pour la Recherche Médicale; European Research Council; BC Children's Hospital; Tokyo University of Agriculture; NODAI Genome Research Center, Tokyo University of Agriculture; Sumitomo Foundation; Children's Hospital Foundation","keywords":"Genomic imprinting; Biology; Imprinting (psychology); Genetics; Gene; DNA methylation; Promoter; Genome; Gene expression","score_opus":0.03974186645115925,"score_gpt":0.3235652243091437,"score_spread":0.28382335785798446,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4324156277","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":[0.9949174,0.001264545,0.0025525393,0.000013261476,0.000003377153,0.0000055448804,0.0002885188,0.000054553788,0.0009004346],"genre_scores_gemma":[0.99607277,0.00034856732,0.0022332638,0.000018550214,0.000005142589,0.0000079114225,0.0004968662,0.000021386522,0.0007956309],"study_design_codex":"bench_or_experimental","study_design_gemma":"not_applicable","domain_scores_codex":[0.99985266,0.000017724598,0.000014481511,0.000055173565,0.00003524722,0.000024773562],"domain_scores_gemma":[0.9996138,0.00009889576,0.00013177734,0.000049010298,0.00003996447,0.00006659917],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00014097836,0.00017777683,0.00022368769,0.00064660865,0.00011974453,0.00024645668,0.00024169969,0.00011778648,0.0009989605],"category_scores_gemma":[0.00035516595,0.000116704585,0.00018247323,0.0002450562,0.00022131993,0.00017679554,0.00039018763,0.00021082978,0.00023790824],"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":[0.00039547493,0.0000135001565,0.05231525,0.00015663197,0.000051660758,0.00033635952,0.00015778685,0.00017356686,0.92361605,0.0006154181,0.000047944304,0.022120396],"study_design_scores_gemma":[0.00001643223,0.00043458436,0.8336187,0.000028636076,0.000081004924,0.0027265179,0.00014273921,0.0009112864,0.15760265,0.0005643927,0.0038487504,0.000024333434],"about_ca_topic_score_codex":0.00056611706,"about_ca_topic_score_gemma":0.00088956195,"teacher_disagreement_score":0.0009989605,"about_ca_system_score_codex":0.00015619594,"about_ca_system_score_gemma":0.00013179668,"threshold_uncertainty_score":0.0033419132},"labels":[],"label_agreement":null},{"id":"W4361266110","doi":"10.1158/0008-5472.c.6494585","title":"Data from The c-Myc Oncogene Directly Induces the H19 Noncoding RNA by Allele-Specific Binding to Potentiate Tumorigenesis","year":2023,"lang":"en","type":"preprint","venue":"","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":0,"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; Ontario Institute for Cancer Research","funders":"Canadian Institutes of Health Research; University of Pennsylvania; U.S. Department of Defense","keywords":"Gene knockdown; Biology; Chromatin immunoprecipitation; Genomic imprinting; Cancer research; Carcinogenesis; Transcription factor; Oncogene; Long non-coding RNA; Gene; Molecular biology; N-Myc; Gene expression; Promoter; DNA methylation; Genetics; RNA; Cell cycle; Cell culture","score_opus":0.08365703510303053,"score_gpt":0.29795378096500286,"score_spread":0.21429674586197234,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4361266110","genre_codex":"empirical","genre_gemma":"dataset","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"dataset","genre_consensus":null,"domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.87721187,0.0075408868,0.01809365,0.0024405853,0.0010184475,0.00034876255,0.044166733,0.0017836941,0.047395397],"genre_scores_gemma":[0.8926748,0.003287335,0.0133558,0.00088164303,0.000095092706,0.0004993347,0.043675266,0.0004476447,0.045083076],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9995004,0.000045883164,0.0000485323,0.00008662617,0.00022154144,0.000097137156],"domain_scores_gemma":[0.9995567,0.00010400169,0.00005151482,0.00007805577,0.000048068956,0.0001617566],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00025042327,0.0007243224,0.00036697034,0.00088193844,0.0004958166,0.0004777054,0.0003429706,0.00053530757,0.01583607],"category_scores_gemma":[0.0002158782,0.00027746163,0.00084864016,0.00039720518,0.00034719834,0.00022124819,0.00035376154,0.0017897093,0.0039096186],"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":[0.00027912954,0.00010053945,0.0002613369,0.00009243386,0.000016426127,0.00007685504,0.000018741488,0.000059506445,0.99638027,0.00022557027,0.0006282431,0.0018610153],"study_design_scores_gemma":[0.000043728018,0.00023766176,0.008395615,0.000012532229,0.000023569031,0.00030849664,0.000033110824,0.00042639396,0.9788669,0.000077502766,0.011566683,0.000007823509],"about_ca_topic_score_codex":0.001769443,"about_ca_topic_score_gemma":0.00340816,"teacher_disagreement_score":0.01583607,"about_ca_system_score_codex":0.0006002388,"about_ca_system_score_gemma":0.0003774412,"threshold_uncertainty_score":0.052976906},"labels":[],"label_agreement":null},{"id":"W4361271943","doi":"10.1016/j.stemcr.2023.03.004","title":"Differentiation of uniparental human embryonic stem cells into granulosa cells reveals a paternal contribution to gonadal development","year":2023,"lang":"en","type":"article","venue":"Stem Cell Reports","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":3,"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":"Azrieli Foundation; Israel Science Foundation; Rosetrees Trust","keywords":"Biology; Genomic imprinting; Parthenogenesis; Sexual differentiation; Induced pluripotent stem cell; Embryonic stem cell; Imprinting (psychology); Genetics; Gonad; Genome; Gene; Stem cell; Cellular differentiation; Embryo; Gene expression; DNA methylation; Endocrinology","score_opus":0.009669179166216433,"score_gpt":0.2306244832353495,"score_spread":0.22095530406913308,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4361271943","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99123114,0.00175228,0.0044548213,0.00009432899,0.000017343327,0.000012982618,0.00045016265,0.000055164943,0.0019317194],"genre_scores_gemma":[0.9943294,0.0011446606,0.0025353376,0.00003970512,0.0000053325202,0.0000070684723,0.00040118498,0.000014435808,0.0015229516],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9999474,0.000009075248,0.000006535883,0.000012606284,0.000016713855,0.000007631506],"domain_scores_gemma":[0.99992335,0.00001692008,0.000023074288,0.000015230607,0.0000053780386,0.000015990425],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00009016846,0.0001383204,0.00010037115,0.00017497475,0.00006383304,0.00017553891,0.00008291841,0.00009491372,0.00074951537],"category_scores_gemma":[0.0001049479,0.00008022918,0.00008251006,0.00012391729,0.00021011996,0.000074793286,0.00018515247,0.00021032382,0.00023101123],"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":[0.000029436573,0.0000023930793,0.0011494003,0.000018284678,0.0000026480109,0.00010020634,0.000017725872,0.000020566253,0.9961486,0.00015810909,0.000014308268,0.0023382981],"study_design_scores_gemma":[0.000008127876,0.00012865271,0.04747465,0.000009139732,0.00002010355,0.0016503873,0.00006815669,0.0003033559,0.9449239,0.00021550208,0.0051944987,0.000003675184],"about_ca_topic_score_codex":0.00025232334,"about_ca_topic_score_gemma":0.0006284464,"teacher_disagreement_score":0.00074951537,"about_ca_system_score_codex":0.000092240814,"about_ca_system_score_gemma":0.000109698696,"threshold_uncertainty_score":0.0025074482},"labels":[],"label_agreement":null},{"id":"W4361298710","doi":"10.1038/s41380-022-01909-9","title":"Focal adhesion is associated with lithium response in bipolar disorder: evidence from a network-based multi-omics analysis","year":2023,"lang":"en","type":"article","venue":"Molecular Psychiatry","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":28,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Dalhousie University","funders":"National Institute of Mental Health; National Institutes of Health; University of California, San Diego; Genome Atlantic; Dalhousie University; Research Nova Scotia; U.S. Department of Veterans Affairs; Paul G. Allen Frontiers Group; National Center for Advancing Translational Sciences; Agence Nationale de la Recherche; Georgia Clinical and Translational Science Alliance; Dalhousie Medical Research Foundation; JPB Foundation; Canadian Institutes of Health Research; American Heart Association","keywords":"Genome-wide association study; Transcriptome; Bipolar disorder; Biology; Computational biology; Gene expression profiling; Candidate gene; Gene regulatory network; Gene; Genetics; Lithium (medication); Bioinformatics; Single-nucleotide polymorphism; Gene expression; Endocrinology","score_opus":0.011765825665352742,"score_gpt":0.25582661969630155,"score_spread":0.2440607940309488,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4361298710","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.97062445,0.011184434,0.0069688116,0.0012864196,0.000043049426,0.00005286753,0.008078552,0.000094397685,0.001666943],"genre_scores_gemma":[0.9903752,0.0020360302,0.003460332,0.00025049452,0.0000346087,0.000049718656,0.003461837,0.000014173586,0.00031761138],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9996346,0.000100639714,0.000033168093,0.00013059306,0.000056317505,0.00004464519],"domain_scores_gemma":[0.99929285,0.00026793923,0.00027050544,0.00004137821,0.00007002296,0.000057231897],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00051917793,0.000389884,0.0005412955,0.0016493739,0.00037525216,0.00083662145,0.0002992301,0.00035693287,0.0019149102],"category_scores_gemma":[0.0010421159,0.00020392684,0.00094091694,0.0018354398,0.00026248448,0.00036006756,0.0005657821,0.00049319747,0.00018524236],"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":[0.0010234629,0.00008482442,0.92120767,0.0007698115,0.0032692316,0.00064909033,0.0002693877,0.0029218204,0.032819167,0.0010531667,0.0026768965,0.03325559],"study_design_scores_gemma":[0.00002956858,0.000071337694,0.9836758,0.00009385868,0.0009144828,0.0004925288,0.00026427908,0.009498784,0.0009913774,0.00213082,0.001816528,0.000020617465],"about_ca_topic_score_codex":0.0036983555,"about_ca_topic_score_gemma":0.005078637,"teacher_disagreement_score":0.0036983555,"about_ca_system_score_codex":0.00040338826,"about_ca_system_score_gemma":0.00032447762,"threshold_uncertainty_score":0.0073536634},"labels":[],"label_agreement":null},{"id":"W4361859041","doi":"10.1177/27528464231166828","title":"Multi-suture craniosynostosis in Sotos Syndrome: A case Report","year":2023,"lang":"en","type":"article","venue":"Craniomaxillofacial Research & Innovation","topic":"Genetic Syndromes and Imprinting","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; Hospital for Sick Children; University of Toronto","funders":"","keywords":"Craniosynostosis; Sotos syndrome; Medicine; Apert syndrome; Craniofacial; Craniosynostoses; Fibrous joint; Presentation (obstetrics); Surgery; Pediatrics; Psychiatry","score_opus":0.08185742521882457,"score_gpt":0.38844126206859964,"score_spread":0.3065838368497751,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4361859041","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.96877444,0.011730199,0.006098108,0.0014307393,0.00036519166,0.0009158238,0.00043997224,0.0001902362,0.01005535],"genre_scores_gemma":[0.9896339,0.00333537,0.0037024922,0.00052558526,0.00073130656,0.00022753794,0.00016082532,0.000030666662,0.0016522912],"study_design_codex":"case_report","study_design_gemma":"case_report","domain_scores_codex":[0.99913496,0.00009479576,0.00015211031,0.00026786723,0.00014664735,0.00020373485],"domain_scores_gemma":[0.99875546,0.00025279727,0.00055245444,0.00010559466,0.00006827568,0.00026545936],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00039690384,0.0019781382,0.0013579961,0.002567758,0.0015959699,0.0014480912,0.0009334338,0.004087633,0.003421481],"category_scores_gemma":[0.0016945589,0.0009478276,0.00089539256,0.0016645518,0.0019052321,0.0014891827,0.0017665557,0.001653743,0.00088371796],"study_design_candidate":"case_report","study_design_consensus":"case_report","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.000022596098,0.00003954307,0.006232156,0.000085648106,0.0000096652775,0.99035335,0.00012928003,0.000052025593,0.0009963507,0.00026501328,0.00018859709,0.0016256898],"study_design_scores_gemma":[0.0000058864744,0.000028580831,0.0016302894,0.000009542743,0.0000073093734,0.9975721,0.00006797766,0.000055771176,0.00013147357,0.00010012977,0.00038483783,0.00000613413],"about_ca_topic_score_codex":0.00080990174,"about_ca_topic_score_gemma":0.00097523566,"teacher_disagreement_score":0.004087633,"about_ca_system_score_codex":0.00070412375,"about_ca_system_score_gemma":0.00085106224,"threshold_uncertainty_score":0.011445999},"labels":[],"label_agreement":null},{"id":"W4362467524","doi":"10.3389/fnins.2023.1189154","title":"Corrigendum: Prader-Willi syndrome: Symptoms and topiramate response in light of genetics","year":2023,"lang":"en","type":"erratum","venue":"Frontiers in Neuroscience","topic":"Genetic Syndromes and Imprinting","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":"McGill University","funders":"","keywords":"Topiramate; Response inhibition; Genetics; Psychology; Medicine; Neuroscience; Biology; Cognition; Epilepsy","score_opus":0.01347448799535661,"score_gpt":0.2436208831035782,"score_spread":0.2301463951082216,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4362467524","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":[0.0002746877,0.00343322,0.00067721104,0.06465516,0.9246048,0.000024745483,0.0007584867,0.000467109,0.0051045422],"genre_scores_gemma":[0.022083731,0.021705039,0.004573043,0.14196198,0.46537668,0.00019327477,0.0033635162,0.0020820105,0.3386607],"study_design_codex":"not_applicable","study_design_gemma":"not_applicable","domain_scores_codex":[0.9970975,0.0003629593,0.0004871828,0.0005085972,0.0012670535,0.00027666392],"domain_scores_gemma":[0.9893875,0.0020826466,0.00069362164,0.0005479045,0.0065347445,0.0007536066],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0018756872,0.0023420178,0.0023280713,0.002475047,0.0026568118,0.003206303,0.0030972634,0.0073674605,0.06633183],"category_scores_gemma":[0.023755854,0.000988911,0.0015611494,0.0015081951,0.0025308814,0.002148014,0.0018926582,0.008588676,0.05042591],"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":[0.00002949308,0.000006253538,0.00008525539,0.000105910985,0.0000108904205,0.0006928267,0.000024907984,0.000030202942,0.000087209024,0.0003769279,0.992724,0.0058262073],"study_design_scores_gemma":[0.000024065464,0.000029987337,0.0010278374,0.0003043975,0.000053039712,0.0036385902,0.00010628839,0.00018325132,0.0009971876,0.0009886153,0.992597,0.000049837316],"about_ca_topic_score_codex":0.012099052,"about_ca_topic_score_gemma":0.01544137,"teacher_disagreement_score":0.06633183,"about_ca_system_score_codex":0.0042441315,"about_ca_system_score_gemma":0.0025606113,"threshold_uncertainty_score":0.22190207},"labels":[],"label_agreement":null},{"id":"W4366601899","doi":"10.1111/pcmr.13089","title":"<scp>BORIS</scp> / <scp>CTCFL</scp> ‐mediated chromatin accessibility alterations promote a pro‐invasive transcriptional signature in melanoma cells","year":2023,"lang":"en","type":"article","venue":"Pigment Cell & Melanoma Research","topic":"Genetic Syndromes and Imprinting","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":"McGill University Health Centre; McGill University; Jewish General Hospital","funders":"Canadian Institutes of Health Research; Israel Science Foundation; Israel Cancer Research Fund","keywords":"Chromatin; Melanoma; Ectopic expression; Biology; Reprogramming; Transcription factor; Bivalent chromatin; Promoter; Cancer research; Chromatin immunoprecipitation; Transcriptional regulation; Cell biology; Regulation of gene expression; Gene; Gene expression; Chromatin remodeling; Genetics","score_opus":0.0338307159432611,"score_gpt":0.30853544248746506,"score_spread":0.27470472654420397,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4366601899","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.98930746,0.00071045593,0.0059012184,0.00008542314,0.000025003254,0.00002013927,0.0013577676,0.00031224618,0.0022802728],"genre_scores_gemma":[0.9941409,0.00025950422,0.0017454604,0.000056851542,0.000004832399,0.000017104949,0.0010943421,0.00006229456,0.002618684],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99989676,0.000007850011,0.0000052277283,0.000033945555,0.000035807174,0.00002037579],"domain_scores_gemma":[0.9999223,0.000013946976,0.00002563527,0.000010942995,0.0000066362236,0.000020529074],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.000082051534,0.00018181413,0.0001330899,0.0001948371,0.00014165332,0.0002650205,0.0001040624,0.0001747505,0.0019674478],"category_scores_gemma":[0.00008696256,0.00013885774,0.0001646134,0.0001513568,0.00019988953,0.00010222477,0.0002164165,0.0004181965,0.0005827364],"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":[0.0000173072,0.000002147077,0.0001942494,0.000007426164,0.0000019538027,0.00003359673,0.0000048933543,0.000035383742,0.99921453,0.000046387908,0.000031103235,0.00041108797],"study_design_scores_gemma":[0.000008183347,0.00004687518,0.024829542,0.000004775239,0.000009254456,0.00039329883,0.000037501286,0.0016609078,0.969348,0.00009082122,0.003565015,0.000005785417],"about_ca_topic_score_codex":0.0011718611,"about_ca_topic_score_gemma":0.0023123578,"teacher_disagreement_score":0.0019674478,"about_ca_system_score_codex":0.00021477159,"about_ca_system_score_gemma":0.00014265082,"threshold_uncertainty_score":0.0065817833},"labels":[],"label_agreement":null},{"id":"W4367055664","doi":"10.1111/age.13326","title":"Association between TH/MAOB gene single nucleotide polymorphisms and excitability in Labrador Retrievers","year":2023,"lang":"en","type":"article","venue":"Animal Genetics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":2,"is_retracted":false,"has_abstract":true,"route_ca_aff":false,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":true,"ca_institutions":"","funders":"National Key Research and Development Program of China","keywords":"Biology; Genetics; Single-nucleotide polymorphism; Gene; Genotype","score_opus":0.017531844249562497,"score_gpt":0.24093426038299606,"score_spread":0.22340241613343356,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4367055664","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99972326,0.0000789044,0.00002724191,0.0000060843145,6.3597855e-7,0.0000014203333,0.000045964873,0.00000141541,0.00011506895],"genre_scores_gemma":[0.999595,0.000042561045,0.00007135822,0.000008692142,0.0000032965006,0.0000034079935,0.00008616306,0.0000014361926,0.00018805318],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9998716,0.000019015082,0.000018637269,0.00004679943,0.000024827887,0.000019188577],"domain_scores_gemma":[0.9998036,0.000030548195,0.000106245774,0.000015804453,0.000014434529,0.000029479395],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00018940221,0.00019829912,0.00022589593,0.0005209973,0.00017776752,0.00026594845,0.00015567256,0.0002970423,0.0008770537],"category_scores_gemma":[0.00029934224,0.00012205489,0.00026552,0.00030485966,0.00017004272,0.00010288125,0.00010595032,0.00018220497,0.00011289283],"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":[0.0006767881,0.0000850026,0.9799484,0.00001815192,0.00018726493,0.0004915614,0.00021480516,0.00010916818,0.015372779,0.000041960317,0.00006704402,0.0027870918],"study_design_scores_gemma":[0.000006533655,0.00009809997,0.9989728,0.0000031830102,0.000038136855,0.000294256,0.000051498428,0.00018757496,0.0002622754,0.000012481031,0.0000711906,0.000002120526],"about_ca_topic_score_codex":0.0039325743,"about_ca_topic_score_gemma":0.0049715373,"teacher_disagreement_score":0.0039325743,"about_ca_system_score_codex":0.00017873137,"about_ca_system_score_gemma":0.00006203523,"threshold_uncertainty_score":0.0078193545},"labels":[],"label_agreement":null},{"id":"W4367311515","doi":"10.3390/ijms24098013","title":"Evaluation of Autonomic Nervous System Dysfunction in Childhood Obesity and Prader–Willi Syndrome","year":2023,"lang":"en","type":"article","venue":"International Journal of Molecular Sciences","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":9,"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":"Canadian Institutes of Health Research","keywords":"Sudomotor; Medicine; Internal medicine; Autonomic nervous system; Heart rate; Body mass index; Heart rate variability; Blood pressure; Valsalva maneuver; Endocrinology; Baroreflex; Obesity; Sympathetic nervous system; Cardiology; SWEAT; Cardiac function curve; Heart failure","score_opus":0.0158908415102191,"score_gpt":0.2718626255902935,"score_spread":0.2559717840800744,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4367311515","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99942684,0.00017976183,0.00012630118,0.0000069909725,0.000002987971,0.0000068271643,0.000038929644,0.000004547833,0.00020687046],"genre_scores_gemma":[0.99929535,0.00021356571,0.00026603788,0.000013419411,0.0000072472,0.000008655633,0.000085200954,0.000002508744,0.00010808584],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99960715,0.00012457986,0.00004632804,0.00008978706,0.00008110666,0.000051005678],"domain_scores_gemma":[0.9994518,0.00014527186,0.0002179101,0.000026406868,0.00003627947,0.00012223555],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00045529183,0.00052886514,0.00039126072,0.0012291683,0.0002823564,0.0002888214,0.00022394421,0.00031963663,0.00090503297],"category_scores_gemma":[0.0013722766,0.00021436243,0.00019722036,0.00048094982,0.00046471134,0.00026306018,0.00042156086,0.0003600401,0.00010650511],"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":[0.00017662605,0.00005286446,0.9857442,0.00003149185,0.00003395246,0.004471918,0.00020812073,0.00006513891,0.005892892,0.00004091057,0.000034164725,0.0032477274],"study_design_scores_gemma":[0.000004050985,0.00019736712,0.99199486,0.0000056388276,0.000015953134,0.0068188678,0.00010311021,0.00009254038,0.0006747963,0.000014691823,0.00007497358,0.0000032052958],"about_ca_topic_score_codex":0.0015700758,"about_ca_topic_score_gemma":0.0015686674,"teacher_disagreement_score":0.0015700758,"about_ca_system_score_codex":0.0001502665,"about_ca_system_score_gemma":0.0002191763,"threshold_uncertainty_score":0.0031217933},"labels":[],"label_agreement":null},{"id":"W4367839824","doi":"10.1002/ajmg.a.63224","title":"Uniparental disomy of multiple chromosomes in two cases with a complex phenotype","year":2023,"lang":"en","type":"article","venue":"American Journal of Medical Genetics Part A","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","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":"Women's Health Research Institute","funders":"","keywords":"Uniparental disomy; Biology; Genetics; Imprinting (psychology); Aneuploidy; Genomic imprinting; Phenotype; Chromosome; Trisomy; Karyotype; DNA methylation; Gene","score_opus":0.023218995591417393,"score_gpt":0.3083044668812433,"score_spread":0.2850854712898259,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4367839824","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9941453,0.0009265687,0.001307178,0.00038766468,0.00006474469,0.000077175006,0.0001166592,0.00008361575,0.0028912392],"genre_scores_gemma":[0.99757034,0.00026382017,0.0010628749,0.00012990198,0.00010414769,0.00002643497,0.000102043436,0.00002656502,0.00071378157],"study_design_codex":"case_report","study_design_gemma":"case_report","domain_scores_codex":[0.9993191,0.00006864034,0.00009933101,0.00019328142,0.00012230407,0.00019735028],"domain_scores_gemma":[0.9975036,0.00062983396,0.0007512985,0.00019147781,0.000100354424,0.0008234664],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00035712466,0.00198175,0.00066284114,0.002953889,0.0009556891,0.0010691554,0.0011894715,0.0024494205,0.0022241455],"category_scores_gemma":[0.004033152,0.0012249809,0.0006599082,0.0010467741,0.0018238514,0.000819481,0.0018989841,0.0015973814,0.0006880082],"study_design_candidate":"case_report","study_design_consensus":"case_report","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.000077811,0.000050428018,0.032341905,0.000027826483,0.00001909827,0.95983493,0.00046075057,0.00009991998,0.004012555,0.00025571804,0.00026806715,0.0025509803],"study_design_scores_gemma":[0.000019021745,0.000054334407,0.019780558,0.000006188816,0.000011039114,0.9784636,0.00007572409,0.00013923422,0.00089502917,0.00012270936,0.00041900954,0.000013554175],"about_ca_topic_score_codex":0.0021951746,"about_ca_topic_score_gemma":0.0025642188,"teacher_disagreement_score":0.002953889,"about_ca_system_score_codex":0.0009194162,"about_ca_system_score_gemma":0.0004768874,"threshold_uncertainty_score":0.0074405074},"labels":[],"label_agreement":null},{"id":"W4381839637","doi":"10.1002/ajmg.a.63337","title":"Five siblings expand the spectrum of <i>GPC6</i>‐related skeletal dysplasia","year":2023,"lang":"en","type":"article","venue":"American Journal of Medical Genetics Part A","topic":"Genetic Syndromes and Imprinting","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":"University of Toronto; Sunnybrook Health Science Centre","funders":"","keywords":"Phenotype; Missense mutation; Short stature; Dysplasia; Biology; Proband; Genetics; Endocrinology; Medicine; Internal medicine; Gene; Mutation","score_opus":0.00747837789242804,"score_gpt":0.2644649982211528,"score_spread":0.25698662032872477,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4381839637","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9918412,0.00028816238,0.0013540947,0.0002812512,0.00004846097,0.00007077378,0.00019534597,0.000107745596,0.0058129104],"genre_scores_gemma":[0.9974915,0.0001591462,0.0008681008,0.00016694228,0.000025893381,0.00001697192,0.0001104733,0.00002368034,0.001137216],"study_design_codex":"case_report","study_design_gemma":"case_report","domain_scores_codex":[0.9994399,0.00008088562,0.00007550867,0.0001554015,0.00014091685,0.00010730381],"domain_scores_gemma":[0.99935395,0.00019631385,0.0001340051,0.000056067645,0.000081508726,0.00017813759],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0003288707,0.0019136145,0.000612549,0.0008963139,0.0011670436,0.00047251064,0.00051488105,0.0008028593,0.0045121396],"category_scores_gemma":[0.0018185178,0.0005467263,0.0005042213,0.0005771154,0.0009664274,0.0004256717,0.0012874294,0.00073280255,0.00058255927],"study_design_candidate":"case_report","study_design_consensus":"case_report","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00022652773,0.0003902053,0.16122292,0.00012520506,0.00009132451,0.7563535,0.0034720642,0.00047562286,0.049416553,0.001814869,0.0016711792,0.02474006],"study_design_scores_gemma":[0.000034652785,0.00038803968,0.09105768,0.00004466009,0.000061525214,0.8958948,0.0006051359,0.00044035364,0.005939264,0.0007469047,0.0047508017,0.000036206875],"about_ca_topic_score_codex":0.0020710297,"about_ca_topic_score_gemma":0.0018229376,"teacher_disagreement_score":0.0045121396,"about_ca_system_score_codex":0.00040134537,"about_ca_system_score_gemma":0.0004366275,"threshold_uncertainty_score":0.015094578},"labels":[],"label_agreement":null},{"id":"W4382560327","doi":"10.1038/s41572-023-00443-4","title":"Imprinting disorders","year":2023,"lang":"en","type":"review","venue":"Nature Reviews Disease Primers","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","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":"Hospital for Sick Children; University of Toronto","funders":"Biotechnology and Biological Sciences Research Council","keywords":"Psychology; Medicine","score_opus":0.030277463018884242,"score_gpt":0.3558298068552445,"score_spread":0.3255523438363603,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4382560327","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":[0.00012454305,0.98892665,0.00069550704,0.0005978451,0.0017302752,0.000010661965,0.00009958143,0.000052258034,0.007762661],"genre_scores_gemma":[0.0014376882,0.9855627,0.0006684775,0.0011473822,0.001618221,0.000017050173,0.00028912563,0.000011681146,0.00924768],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.9998024,0.000030772455,0.000019187597,0.0000401664,0.000079498386,0.000027934622],"domain_scores_gemma":[0.9998234,0.00007939814,0.00002123669,0.000010238199,0.00003720876,0.000028633123],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00039334173,0.0012283203,0.0013293865,0.0016457911,0.0002323277,0.0010671172,0.0010541084,0.0009703111,0.0099311145],"category_scores_gemma":[0.00072433625,0.0002761521,0.00029323442,0.001403693,0.000523594,0.000724272,0.0010603095,0.0018031484,0.0065690926],"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":[0.000057522746,0.000020962982,0.00014509428,0.0025887731,0.000046042824,0.00040041498,0.000023642751,0.0002268275,0.0015560556,0.004565031,0.13385332,0.85651624],"study_design_scores_gemma":[0.000012765974,0.0000132415125,0.0003138115,0.0009623613,0.000039548107,0.0017651066,0.000015050775,0.00004283288,0.00033084434,0.0013086883,0.9951891,0.0000066280436],"about_ca_topic_score_codex":0.0011164491,"about_ca_topic_score_gemma":0.0024566504,"teacher_disagreement_score":0.0099311145,"about_ca_system_score_codex":0.0006320423,"about_ca_system_score_gemma":0.00071365084,"threshold_uncertainty_score":0.033222914},"labels":[],"label_agreement":null},{"id":"W4384563092","doi":"10.1016/j.bonr.2023.101700","title":"Bone mineral density and its relationship with ground reaction force characteristics during gait in young adults with Prader-Willi Syndrome","year":2023,"lang":"en","type":"article","venue":"Bone Reports","topic":"Genetic Syndromes and Imprinting","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":"Western University","funders":"California State University","keywords":"Ground reaction force; Bone mineral; Gait; Medicine; Physical medicine and rehabilitation; Internal medicine; Physics; Osteoporosis","score_opus":0.00916072216521198,"score_gpt":0.21182089288813408,"score_spread":0.20266017072292208,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4384563092","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9997484,0.000074381605,0.000038065227,0.0000066971033,0.0000015205615,0.0000031165637,0.000040264633,0.0000012152768,0.00008630582],"genre_scores_gemma":[0.9996871,0.000046427373,0.00006464344,0.000006537192,0.0000028954414,0.0000047642884,0.00008562558,4.930667e-7,0.000101519916],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99981743,0.000033802433,0.000035268036,0.00004182826,0.000045501114,0.000026163703],"domain_scores_gemma":[0.99953675,0.00009950208,0.00019537918,0.00002159694,0.00006284579,0.00008395089],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00024556115,0.00027570856,0.0002710251,0.0007603869,0.00017504884,0.00022739325,0.00013158421,0.00036047216,0.00086278486],"category_scores_gemma":[0.0015409706,0.00020059693,0.00020067612,0.0003655848,0.00014306561,0.00017612387,0.00028917906,0.00027448006,0.00015803066],"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":[0.000115653085,0.000036014248,0.99711096,0.000006661941,0.000030850922,0.00016025723,0.00009031353,0.000021575675,0.0008953784,0.0000058708165,0.000018268878,0.0015081388],"study_design_scores_gemma":[0.0000023558105,0.00011176282,0.99934417,0.0000015773503,0.000006997885,0.0003416156,0.00006447894,0.00005549206,0.000043073574,0.0000047695726,0.00002277511,0.0000010079458],"about_ca_topic_score_codex":0.002835396,"about_ca_topic_score_gemma":0.0031461676,"teacher_disagreement_score":0.002835396,"about_ca_system_score_codex":0.00008913981,"about_ca_system_score_gemma":0.00007793551,"threshold_uncertainty_score":0.005637765},"labels":[],"label_agreement":null},{"id":"W4385258318","doi":"10.7202/1101833ar","title":"Vers une éthique de la relation de communication avec les personnes atteintes du syndrome d’Angelman","year":2023,"lang":"fr","type":"article","venue":"Nouvelles perspectives en sciences sociales","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":1,"is_retracted":false,"has_abstract":true,"route_ca_aff":false,"route_ca_fund":false,"route_ca_venue":true,"route_about_ca":false,"ca_institutions":"","funders":"","keywords":"Humanities; Political science; Sociology; Philosophy","score_opus":0.01971266041107919,"score_gpt":0.30066621482164135,"score_spread":0.28095355441056213,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4385258318","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.8981256,0.007361341,0.008566087,0.028983152,0.00024269051,0.000060295217,0.00022530988,0.000026359023,0.056409065],"genre_scores_gemma":[0.99337643,0.0014210147,0.00146832,0.00062114827,0.00006672311,0.000036775786,0.00003068146,0.000008402208,0.002970589],"study_design_codex":"qualitative","study_design_gemma":"theoretical_or_conceptual","domain_scores_codex":[0.9962304,0.002588168,0.0001458439,0.00032636672,0.0004591973,0.00024996832],"domain_scores_gemma":[0.9912232,0.0051898,0.0020990127,0.00045700913,0.0006723746,0.00035864286],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0049106944,0.0003444666,0.00036177435,0.0019467532,0.0028456375,0.0025095744,0.00051718473,0.0012048928,0.006553574],"category_scores_gemma":[0.0110447,0.00028705818,0.00030878492,0.0012531464,0.00933079,0.0032215975,0.0023068332,0.0015101511,0.00030301762],"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":[0.00039506244,0.00012010172,0.2130033,0.0005250257,0.000117180796,0.009132854,0.5084172,0.0003547146,0.006686112,0.20084588,0.0024924607,0.05791015],"study_design_scores_gemma":[0.00006524071,0.00034484392,0.3318867,0.0014364065,0.00014636038,0.013397967,0.48177305,0.00087282923,0.0024356253,0.09984221,0.06759316,0.0002056387],"about_ca_topic_score_codex":0.011188614,"about_ca_topic_score_gemma":0.011761283,"teacher_disagreement_score":0.011188614,"about_ca_system_score_codex":0.0022474162,"about_ca_system_score_gemma":0.0028246255,"threshold_uncertainty_score":0.025970519},"labels":[],"label_agreement":null},{"id":"W4385293731","doi":"10.1016/j.humov.2023.103125","title":"Contributing factors to postural stability in Prader-Willi syndrome","year":2023,"lang":"en","type":"article","venue":"Human Movement Science","topic":"Genetic Syndromes and Imprinting","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":"Western University","funders":"California State University, Sacramento; California State University","keywords":"Gait; Balance (ability); Medicine; Physical medicine and rehabilitation; Dynamic balance; Physical therapy; Vestibular system; Proprioception; Sensory system; Somatosensory system; Psychology; Audiology","score_opus":0.030043446840477196,"score_gpt":0.29442643094762094,"score_spread":0.2643829841071437,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4385293731","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99948657,0.00016478729,0.0001257737,0.000014185021,0.0000040023324,0.0000044833187,0.000030063016,0.0000028764828,0.00016711483],"genre_scores_gemma":[0.99963164,0.00009799958,0.00012062158,0.000009021908,0.0000059683857,0.000003744993,0.000054733297,0.000001143898,0.00007501516],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99973375,0.00004768095,0.000038075013,0.000061213046,0.0000904489,0.000028826284],"domain_scores_gemma":[0.9996419,0.00006669949,0.00018076296,0.000014292159,0.00004511689,0.00005117633],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00020840624,0.0004395644,0.00039870746,0.000763368,0.00024128638,0.00024728544,0.00014800546,0.0002609352,0.0010995393],"category_scores_gemma":[0.0015637021,0.00015018859,0.00026819657,0.00033983792,0.00021861486,0.0001771808,0.00039162175,0.0002145753,0.00012170391],"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":[0.00016431345,0.00003550841,0.98069096,0.00003193437,0.000069811635,0.0018950267,0.00024454348,0.000059521564,0.00618452,0.00002938665,0.000066251,0.010528152],"study_design_scores_gemma":[0.0000027427122,0.0001214429,0.99651307,0.000006825664,0.00001504531,0.0028685792,0.00010673429,0.000109127956,0.00017476323,0.000018481742,0.00006037957,0.000002854816],"about_ca_topic_score_codex":0.0026081796,"about_ca_topic_score_gemma":0.00478257,"teacher_disagreement_score":0.0026081796,"about_ca_system_score_codex":0.00010933475,"about_ca_system_score_gemma":0.00012336846,"threshold_uncertainty_score":0.0051860213},"labels":[],"label_agreement":null},{"id":"W4386163647","doi":"10.5114/ada.2023.130520","title":"Micronutrient deficiency with skin and systemic symptoms: a case report of acrodermatitis enteropathica","year":2023,"lang":"en","type":"article","venue":"Advances in Dermatology and Allergology","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":0,"is_retracted":false,"has_abstract":true,"route_ca_aff":false,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":true,"ca_institutions":"","funders":"Uniwersytet Łódzki","keywords":"Acrodermatitis enteropathica; Medicine; Micronutrient; Dermatology; Micronutrient deficiency; Nutritional deficiency; Internal medicine; Pathology; Zinc deficiency (plant disorder); Malnutrition","score_opus":0.0038063530549514385,"score_gpt":0.23452844538153617,"score_spread":0.23072209232658472,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4386163647","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.93036634,0.043873172,0.005082956,0.0053264806,0.0009867799,0.00033292203,0.0004132428,0.00043565544,0.013182588],"genre_scores_gemma":[0.98767453,0.0060124113,0.0016522264,0.0011760935,0.0013163334,0.000056938374,0.00011653174,0.0000450827,0.0019498046],"study_design_codex":"case_report","study_design_gemma":"case_report","domain_scores_codex":[0.99857426,0.00013386236,0.0001857926,0.000407357,0.00019396725,0.000504819],"domain_scores_gemma":[0.9980768,0.00048615312,0.00046773622,0.00021794363,0.00012806381,0.0006234024],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00064195215,0.003401987,0.002854682,0.004670535,0.003592005,0.0028957152,0.001954997,0.0064677503,0.003269175],"category_scores_gemma":[0.0024907177,0.0033257722,0.0023913272,0.0037634377,0.002505187,0.0037741617,0.0029790732,0.0046967072,0.0014251093],"study_design_candidate":"case_report","study_design_consensus":"case_report","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.000020124271,0.000024005409,0.0018582823,0.000030378716,0.000010068524,0.9969524,0.00010519014,0.000017090508,0.00031740626,0.000045634875,0.0001354432,0.0004838811],"study_design_scores_gemma":[0.00000811938,0.000017107894,0.001147604,0.00001015455,0.000010008012,0.99836546,0.000075798074,0.000042022944,0.00007920484,0.000051920222,0.00018661669,0.00000601849],"about_ca_topic_score_codex":0.0026136083,"about_ca_topic_score_gemma":0.0025946025,"teacher_disagreement_score":0.0064677503,"about_ca_system_score_codex":0.0017064663,"about_ca_system_score_gemma":0.0011311366,"threshold_uncertainty_score":0.012381315},"labels":[],"label_agreement":null},{"id":"W4386474232","doi":"10.1126/sciadv.adi2050","title":"Establishment of paternal methylation imprint at the<i>H19/Igf2</i>imprinting control region","year":2023,"lang":"en","type":"article","venue":"Science Advances","topic":"Genetic Syndromes and Imprinting","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":"Cegep de Saint Hyacinthe","funders":"National Institute of General Medical Sciences; Österreichischen Akademie der Wissenschaften","keywords":"CTCF; Imprinting (psychology); Genomic imprinting; Germline; Biology; Allele; DNA methylation; Genetics; Methylation; Epigenetics; Transcription factor; Enhancer; Gene; Gene expression","score_opus":0.011732794425499926,"score_gpt":0.27135333768446734,"score_spread":0.25962054325896744,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4386474232","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.97668266,0.00060055836,0.015187751,0.00013980953,0.000038909293,0.000013590283,0.0002436706,0.0002983929,0.0067945817],"genre_scores_gemma":[0.9958175,0.00014013828,0.0022496772,0.00002884857,0.0000043983923,0.000004196051,0.00012105054,0.000021134383,0.0016130371],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9998957,0.000011328026,0.000006723972,0.000028641965,0.000032548527,0.000025103935],"domain_scores_gemma":[0.99987555,0.000019527057,0.000036741636,0.000021587515,0.00000978792,0.000036895715],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00010397768,0.0002608526,0.00012951555,0.00015814733,0.00011937993,0.00019455398,0.00023104933,0.00020477697,0.0012438986],"category_scores_gemma":[0.00011812718,0.0001247152,0.00019720552,0.00006398546,0.00037701777,0.00021173933,0.0002706982,0.00049118313,0.00027364888],"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":[0.000030968284,0.0000040511513,0.0013674662,0.00000933579,0.000002752904,0.00019385436,0.000014929965,0.000046310393,0.9960581,0.0007356051,0.000018956222,0.0015177226],"study_design_scores_gemma":[0.000007756348,0.000084524094,0.021905676,0.000003860894,0.000009421645,0.00068189186,0.00002825255,0.0006721461,0.9744042,0.00031355282,0.001884356,0.000004325844],"about_ca_topic_score_codex":0.001211258,"about_ca_topic_score_gemma":0.0019885302,"teacher_disagreement_score":0.0012438986,"about_ca_system_score_codex":0.0002618306,"about_ca_system_score_gemma":0.0002478836,"threshold_uncertainty_score":0.0041612387},"labels":[],"label_agreement":null},{"id":"W4386979591","doi":"10.1093/hmg/ddad160","title":"Higher incidence of embryonic defects in mouse offspring conceived with assisted reproduction from fathers with sperm epimutations","year":2023,"lang":"en","type":"article","venue":"Human Molecular Genetics","topic":"Genetic Syndromes and Imprinting","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":"Health Canada; McGill University; McGill University Health Centre","funders":"Health Canada; Canadian Institutes of Health Research; Genome Canada; Alliance de recherche numérique du Canada; Génome Québec; McGill University","keywords":"Biology; Offspring; Haploinsufficiency; Reproductive technology; DNA methylation; Epigenetics; Andrology; Genomic imprinting; Embryo; Sperm; Infertility; Genetics; Epigenome; Fertilisation; Assisted reproductive technology; Embryo culture; Pregnancy; Embryogenesis; Phenotype; Gene","score_opus":0.0183436499955824,"score_gpt":0.2577326108397527,"score_spread":0.23938896084417027,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4386979591","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9764099,0.0029998953,0.012225391,0.00020410806,0.00014579964,0.0000769796,0.0032109711,0.0005545249,0.004172402],"genre_scores_gemma":[0.9708407,0.0014948511,0.0060722046,0.00022156988,0.000023323337,0.0001841195,0.0033378468,0.00024703576,0.017578335],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9993925,0.000086512795,0.00006676933,0.00023027766,0.00015827431,0.000065687294],"domain_scores_gemma":[0.9993273,0.00016186097,0.00018605366,0.000098945326,0.00004922649,0.0001766423],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00038062857,0.00046329046,0.00033763627,0.0008761015,0.00021271528,0.00034958386,0.0003280462,0.00077193475,0.005111139],"category_scores_gemma":[0.00029726187,0.00031520092,0.0005231106,0.00022886164,0.00039180694,0.00023953564,0.00043401858,0.001241013,0.0006978828],"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":[0.00038869033,0.000088212844,0.0033520162,0.00008289154,0.000038924467,0.00056782574,0.00008562441,0.00007783687,0.9908557,0.0004175813,0.00019262974,0.0038519888],"study_design_scores_gemma":[0.000049738184,0.0009705313,0.042472195,0.00004131171,0.000099387,0.004432374,0.00009678269,0.0013195481,0.9438129,0.00025178373,0.006428134,0.000025408674],"about_ca_topic_score_codex":0.000529819,"about_ca_topic_score_gemma":0.00071687053,"teacher_disagreement_score":0.005111139,"about_ca_system_score_codex":0.00018491976,"about_ca_system_score_gemma":0.00020075479,"threshold_uncertainty_score":0.017098427},"labels":[],"label_agreement":null},{"id":"W4387007789","doi":"10.1016/j.humimm.2023.08.026","title":"P124 Like mother, not like daughter? Discovery of a novel DPA1 allele due to discrepant HLA typing between a patient and her daughter","year":2023,"lang":"en","type":"article","venue":"Human Immunology","topic":"Genetic Syndromes and Imprinting","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":"Calgary Laboratory Services; Alberta Biodiversity Monitoring Institute; Alberta Hospital Edmonton; University of Alberta","funders":"","keywords":"Daughter; Typing; Human leukocyte antigen; Allele; Biology; Genetics; Evolutionary biology; Gene; Antigen","score_opus":0.02087135998219418,"score_gpt":0.2581338103177378,"score_spread":0.2372624503355436,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4387007789","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99559915,0.0003436281,0.00042376822,0.0009483217,0.00010375413,0.000014685771,0.000114199116,0.000018511058,0.0024339743],"genre_scores_gemma":[0.9984394,0.00014394535,0.00034147222,0.0002008028,0.00005720342,0.000005575223,0.000047516332,0.000009823867,0.00075430534],"study_design_codex":"case_report","study_design_gemma":"case_report","domain_scores_codex":[0.9996892,0.00004196789,0.00003483251,0.00010709378,0.000050325034,0.00007661008],"domain_scores_gemma":[0.9992899,0.00035250655,0.0001236012,0.000043408672,0.000036127905,0.0001543853],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00022225863,0.00071618013,0.0004164034,0.00084207044,0.0006355531,0.00073198415,0.0007170693,0.0019617316,0.0034401189],"category_scores_gemma":[0.0023251902,0.00032866446,0.00039815748,0.00048659713,0.00062584213,0.00047061776,0.00052427314,0.0012544714,0.0006733987],"study_design_candidate":"case_report","study_design_consensus":"case_report","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0002496582,0.00008489325,0.031509936,0.00003380348,0.000025497184,0.93595594,0.0007067988,0.00008079192,0.02532163,0.0008097006,0.0005251799,0.004696169],"study_design_scores_gemma":[0.000031317377,0.00020084863,0.023158526,0.000015143358,0.000032838896,0.9661542,0.00052062026,0.0003401686,0.007066886,0.000379131,0.0020863535,0.0000139703],"about_ca_topic_score_codex":0.0005538923,"about_ca_topic_score_gemma":0.00026044034,"teacher_disagreement_score":0.0034401189,"about_ca_system_score_codex":0.00036865025,"about_ca_system_score_gemma":0.0001803474,"threshold_uncertainty_score":0.011508346},"labels":[],"label_agreement":null},{"id":"W4387107787","doi":"10.1016/j.gtc.2023.08.005","title":"Management of Monogenic and Syndromic Obesity","year":2023,"lang":"en","type":"review","venue":"Gastroenterology Clinics of North America","topic":"Genetic Syndromes and Imprinting","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":"University of Alberta","funders":"","keywords":"Medicine; Ciliopathies; Leptin receptor; Bardet–Biedl syndrome; Leptin; Proopiomelanocortin; Obesity; Proprotein convertase; Population; Genetics; Internal medicine; Bioinformatics; Endocrinology; Gene; Receptor; Biology; LDL receptor; Phenotype","score_opus":0.025486957283478273,"score_gpt":0.3056754722720263,"score_spread":0.280188514988548,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4387107787","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":[0.00016591522,0.99835855,0.0002864785,0.00034195732,0.00022632595,0.0000029249754,0.00000976627,0.0000087643175,0.0005992716],"genre_scores_gemma":[0.0018040125,0.99595463,0.0005689028,0.00041463843,0.000744791,0.000007200496,0.000046798814,0.0000023992784,0.00045651355],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.99984145,0.000035816396,0.000022744498,0.000024823565,0.000055959175,0.000019266536],"domain_scores_gemma":[0.99979705,0.00009927754,0.00003487709,0.000005319245,0.00003072092,0.000032747783],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0004733399,0.000981113,0.0013536627,0.0018891717,0.00020122297,0.0008239571,0.0009655134,0.0010723977,0.0014493825],"category_scores_gemma":[0.00080927147,0.00018281737,0.00052385335,0.0008850056,0.0003381061,0.00067461154,0.0006748128,0.001940326,0.000760301],"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":[0.00010128773,0.00006666772,0.0004896389,0.005027164,0.00010766436,0.0019132273,0.000024729905,0.00044769634,0.0006475782,0.0013447122,0.02462647,0.96520317],"study_design_scores_gemma":[0.00020013773,0.00027643857,0.005842855,0.012545524,0.0006357505,0.036448732,0.00021209454,0.0008137598,0.0009351202,0.005774346,0.936243,0.00007225181],"about_ca_topic_score_codex":0.0006515684,"about_ca_topic_score_gemma":0.001284102,"teacher_disagreement_score":0.0018891717,"about_ca_system_score_codex":0.00037538132,"about_ca_system_score_gemma":0.00052853784,"threshold_uncertainty_score":0.004848659},"labels":[],"label_agreement":null},{"id":"W4387126575","doi":"10.25011/cim.v46i3.41654","title":"<i>H19</i> Promoter DNA Methylation is Lower Among Early Abortion Patients Undergoing IVF Embryo Transfer","year":2023,"lang":"en","type":"article","venue":"Clinical and investigative medicine","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":2,"is_retracted":false,"has_abstract":true,"route_ca_aff":false,"route_ca_fund":false,"route_ca_venue":true,"route_about_ca":false,"ca_institutions":"","funders":"Binzhou Medical University; Health Commission of Guizhou Province","keywords":"DNA methylation; CpG site; Methylation; Biology; Epigenetics; Bisulfite sequencing; Andrology; Genomic imprinting; Molecular biology; DNMT1; Embryo; Chorionic villi; Gene expression; Placenta; Genetics; Gene; Pregnancy; Fetus; Medicine","score_opus":0.058576794826459784,"score_gpt":0.3041478477299784,"score_spread":0.2455710529035186,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4387126575","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.999171,0.00032675522,0.00007251743,0.000037457936,0.0000040390228,0.0000030212195,0.00009156516,0.0000025830698,0.000290981],"genre_scores_gemma":[0.99966335,0.00008344497,0.000039715305,0.000014600722,0.000006173373,0.00000342619,0.00007913372,0.0000011137179,0.00010904022],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9998858,0.000023069262,0.000014964059,0.000031263055,0.000023816252,0.000020993248],"domain_scores_gemma":[0.9994087,0.00014711102,0.00031127015,0.000017776489,0.000042787957,0.00007235416],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00012529474,0.00012254936,0.00022028519,0.00028727227,0.00016605161,0.00022414244,0.00012448576,0.000291106,0.002595328],"category_scores_gemma":[0.0014182904,0.00009150988,0.00015226951,0.00022333821,0.00013513598,0.00013291233,0.00010531815,0.00026007261,0.00021349962],"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":[0.00038913987,0.000021344924,0.9910334,0.000025542195,0.00004287813,0.00039125705,0.00013726276,0.00002952783,0.0038990942,0.000020649439,0.00012585313,0.0038840151],"study_design_scores_gemma":[0.000009661087,0.000120884164,0.9972504,0.0000070738524,0.00004327668,0.00144921,0.00013077639,0.00013321679,0.0005725623,0.000030636387,0.00024905294,0.0000032277549],"about_ca_topic_score_codex":0.0006811107,"about_ca_topic_score_gemma":0.00056914845,"teacher_disagreement_score":0.002595328,"about_ca_system_score_codex":0.00011095652,"about_ca_system_score_gemma":0.000090228066,"threshold_uncertainty_score":0.008682251},"labels":[],"label_agreement":null},{"id":"W4387380018","doi":"10.1210/jendso/bvad114.535","title":"SAT239 Deceased Donor Parathyroid Allotransplant For Sever Refractory Iatrogenic Hypoparathyroidism","year":2023,"lang":"en","type":"article","venue":"Journal of the Endocrine Society","topic":"Genetic Syndromes and Imprinting","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":"University of Toronto","funders":"","keywords":"Medicine; Hypoparathyroidism; Surgery; Transplantation; Refractory (planetary science); Thyroidectomy; Parathyroid hormone; Calcium; Urology; Internal medicine; Thyroid","score_opus":0.013135653093870554,"score_gpt":0.25808794207897645,"score_spread":0.2449522889851059,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4387380018","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9530862,0.013053015,0.0037792453,0.0047901813,0.0008203975,0.000113196555,0.00039501852,0.00035427755,0.023608364],"genre_scores_gemma":[0.99455935,0.0014240595,0.00060406246,0.00049243006,0.00037217498,0.000016936512,0.00020022897,0.000016229076,0.002314598],"study_design_codex":"case_report","study_design_gemma":"case_report","domain_scores_codex":[0.99991393,0.000007997253,0.00001267843,0.000016038292,0.000019030489,0.000030372466],"domain_scores_gemma":[0.99978274,0.00004212982,0.000029235542,0.00002070524,0.000010115024,0.00011514133],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00014976627,0.00045808076,0.0005039767,0.00067313627,0.00093217316,0.00048184325,0.00043606764,0.00097083824,0.0053537535],"category_scores_gemma":[0.00037957972,0.0001545236,0.000616864,0.0003934634,0.00030688551,0.00043148547,0.00044119006,0.0012534286,0.0012397894],"study_design_candidate":"case_report","study_design_consensus":"case_report","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00030138556,0.0002008963,0.012633938,0.000121560646,0.000039186198,0.95686615,0.00012398268,0.00017559825,0.010170227,0.000381266,0.0014599141,0.017525855],"study_design_scores_gemma":[0.000054637796,0.00043827613,0.014255364,0.000028224733,0.000021386575,0.9794837,0.00006762707,0.00046920966,0.0016249882,0.00029582836,0.0032491332,0.00001163003],"about_ca_topic_score_codex":0.00035405558,"about_ca_topic_score_gemma":0.00069597695,"teacher_disagreement_score":0.0053537535,"about_ca_system_score_codex":0.0005333279,"about_ca_system_score_gemma":0.00038719588,"threshold_uncertainty_score":0.017910063},"labels":[],"label_agreement":null},{"id":"W4387405660","doi":"10.1210/jendso/bvad114.1504","title":"FRI597 Impact Of Theophylline On BMI In Pseudohypoparathyroidism Type 1a - Results Of An Open Label Extension Trial","year":2023,"lang":"en","type":"article","venue":"Journal of the Endocrine Society","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":0,"is_retracted":false,"has_abstract":true,"route_ca_aff":false,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":true,"ca_institutions":"","funders":"","keywords":"GNAS complex locus; Medicine; Theophylline; Internal medicine; Placebo; Endocrinology; Randomized controlled trial; Pediatrics; Biology; Genetics; Pathology","score_opus":0.0470399291479838,"score_gpt":0.36809215505548765,"score_spread":0.3210522259075038,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4387405660","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.96756953,0.013132283,0.0006135942,0.0016629806,0.00074450875,0.0057252445,0.004148313,0.000119655146,0.0062838327],"genre_scores_gemma":[0.9815611,0.0040611397,0.0010812735,0.001396543,0.0005804997,0.005123325,0.0025719705,0.000026186777,0.0035980258],"study_design_codex":"randomized_trial","study_design_gemma":"nonrandomized_trial","domain_scores_codex":[0.99933666,0.00036066887,0.000052653897,0.00009012923,0.000061170285,0.00009871157],"domain_scores_gemma":[0.998804,0.0003417945,0.0002492407,0.00010827302,0.00010375749,0.00039302977],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0020299088,0.0010266985,0.0022835233,0.000284886,0.00032710744,0.0010801799,0.00070931006,0.0018445037,0.008899439],"category_scores_gemma":[0.0019816426,0.00028939004,0.002306594,0.00025815208,0.0006372869,0.000968553,0.0003729741,0.0024247216,0.0011084055],"study_design_candidate":"nonrandomized_trial","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.9716974,0.005316277,0.0010089623,0.0010105242,0.0014106649,0.000067572866,0.000046862857,0.00019573547,0.0025458843,0.00013589929,0.0010709342,0.015493412],"study_design_scores_gemma":[0.9028194,0.087368414,0.006097768,0.00011887667,0.0010715423,0.000057997062,0.000045050023,0.00037965114,0.0003445047,0.00017859224,0.0014970554,0.00002116605],"about_ca_topic_score_codex":0.0006677318,"about_ca_topic_score_gemma":0.0014395342,"teacher_disagreement_score":0.008899439,"about_ca_system_score_codex":0.00065893255,"about_ca_system_score_gemma":0.00073781377,"threshold_uncertainty_score":0.029771626},"labels":[],"label_agreement":null},{"id":"W4387934009","doi":"10.1016/j.jcjd.2023.10.245","title":"CASE REPORT: UNCONTROLLED HYPERTHYROIDISM IN PREGNANCY ASSOCIATED WITH FETAL HEART MALFORMATION","year":2023,"lang":"en","type":"article","venue":"Canadian Journal of Diabetes","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":0,"is_retracted":false,"has_abstract":false,"route_ca_aff":false,"route_ca_fund":false,"route_ca_venue":true,"route_about_ca":false,"ca_institutions":"","funders":"","keywords":"Medicine; Fetus; Fetal heart; Pregnancy; Obstetrics","score_opus":0.00930572246304908,"score_gpt":0.20480487173414708,"score_spread":0.195499149271098,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4387934009","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9142331,0.009968481,0.008141234,0.031095544,0.0030325747,0.00051387365,0.0012713396,0.00052510796,0.03121869],"genre_scores_gemma":[0.9846282,0.002321216,0.002369053,0.0017622735,0.0049322573,0.0000673978,0.00017929828,0.000054785138,0.0036854143],"study_design_codex":"case_report","study_design_gemma":"case_report","domain_scores_codex":[0.9989936,0.00011451135,0.00011718912,0.00031686117,0.0001351879,0.0003226525],"domain_scores_gemma":[0.9962792,0.00140646,0.0006347031,0.00034822072,0.00015806875,0.0011733365],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00053656066,0.0032061264,0.0018797016,0.00400558,0.003464475,0.002143343,0.002753398,0.009414497,0.0038620206],"category_scores_gemma":[0.007194871,0.0016125106,0.002009225,0.0021155684,0.0030677698,0.0018786257,0.0025973446,0.0063126413,0.00092780695],"study_design_candidate":"case_report","study_design_consensus":"case_report","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.000018478007,0.000015171991,0.0012097263,0.000008744165,0.000002808874,0.9980197,0.000043115222,0.000037241836,0.000115829935,0.000120605684,0.00010488231,0.00030369696],"study_design_scores_gemma":[0.000010776428,0.00003364756,0.0014254968,0.000005285586,0.000007363723,0.99775106,0.00006372951,0.00013155122,0.00016049859,0.00018221594,0.00021875653,0.000009607862],"about_ca_topic_score_codex":0.007141362,"about_ca_topic_score_gemma":0.00562216,"teacher_disagreement_score":0.009414497,"about_ca_system_score_codex":0.0025221328,"about_ca_system_score_gemma":0.0018293607,"threshold_uncertainty_score":0.0182994},"labels":[],"label_agreement":null},{"id":"W4388125647","doi":"10.1038/s41596-023-00898-5","title":"EpiTyping: analysis of epigenetic aberrations in parental imprinting and X-chromosome inactivation using RNA-seq","year":2023,"lang":"en","type":"review","venue":"Nature Protocols","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":5,"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":"Horizon 2020 Framework Programme; Azrieli Foundation; Israel Science Foundation; United States-Israel Binational Science Foundation; Rosetrees Trust; European Commission","keywords":"Epigenetics; Biology; Genomic imprinting; Imprinting (psychology); Genetics; Computational biology; Induced pluripotent stem cell; Bacterial artificial chromosome; X-inactivation; Gene; DNA methylation; Genome; Embryonic stem cell; X chromosome; Gene expression","score_opus":0.06462302765635829,"score_gpt":0.4095442324961036,"score_spread":0.3449212048397453,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4388125647","genre_codex":"review","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":[0.0021923662,0.8567612,0.10419011,0.0036945972,0.0042512245,0.00042153263,0.0040979227,0.002810231,0.02158087],"genre_scores_gemma":[0.0064170803,0.86805344,0.078433335,0.0034387729,0.00107713,0.0008567975,0.006131849,0.00080435653,0.034787312],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.9992035,0.00010569353,0.000043165663,0.00013333482,0.00045375252,0.00006062931],"domain_scores_gemma":[0.9991866,0.00037773777,0.000072436094,0.00006767026,0.00022786389,0.000067746325],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0022153293,0.0014803481,0.001216136,0.0016791358,0.0003647368,0.0013636468,0.0023103796,0.0012914969,0.004747227],"category_scores_gemma":[0.001469345,0.0009723554,0.0006158013,0.0016553507,0.00086151075,0.0011465439,0.0014665024,0.0028164324,0.006505302],"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":[0.00008123409,0.0000602675,0.0002933392,0.005023034,0.00010035692,0.00012065085,0.00006914587,0.00079303543,0.055617098,0.009152053,0.082682826,0.84600705],"study_design_scores_gemma":[0.000023314295,0.00005344748,0.0010559832,0.0007108825,0.0000752078,0.00051724305,0.00003702774,0.0009895911,0.038944185,0.005026438,0.9525056,0.00006112474],"about_ca_topic_score_codex":0.0015820798,"about_ca_topic_score_gemma":0.004090528,"teacher_disagreement_score":0.004747227,"about_ca_system_score_codex":0.0008674717,"about_ca_system_score_gemma":0.0011023843,"threshold_uncertainty_score":0.015881121},"labels":[],"label_agreement":null},{"id":"W4388214035","doi":"10.1101/2023.10.30.564869","title":"Post-fertilization transcription initiation in an ancestral LTR retrotransposon drives lineage-specific genomic imprinting of <i>ZDBF2</i>","year":2023,"lang":"en","type":"preprint","venue":"bioRxiv (Cold Spring Harbor Laboratory)","topic":"Genetic Syndromes and Imprinting","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":"University of British Columbia","funders":"NODAI Genome Research Center, Tokyo University of Agriculture; Japan Society for the Promotion of Science; Tokyo University of Agriculture; Ministry of Education, Culture, Sports, Science and Technology","keywords":"Retrotransposon; Biology; Genomic imprinting; Genetics; DNA methylation; Epigenetics; Gene; Long terminal repeat; Exon; Genome; Transposable element; Gene expression","score_opus":0.023161678223940645,"score_gpt":0.2361491103900183,"score_spread":0.21298743216607766,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4388214035","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9936585,0.00048251468,0.0035785022,0.00005249231,0.000022216045,0.000013495185,0.0003313752,0.00013213289,0.0017287574],"genre_scores_gemma":[0.9953336,0.00012089691,0.0012853085,0.000035363755,0.000005535985,0.0000072264584,0.00051050057,0.000038474434,0.0026631043],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.999894,0.0000135704095,0.0000064801366,0.000040636616,0.000020016385,0.000025322006],"domain_scores_gemma":[0.9999193,0.000019221656,0.000026365105,0.000010900715,0.0000057719276,0.000018497542],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00009226897,0.00017688119,0.00009700045,0.00014511109,0.0001231125,0.00021935337,0.00020605102,0.00019642578,0.0019233084],"category_scores_gemma":[0.000085358144,0.00014869634,0.0001776206,0.00007031117,0.00016244262,0.00009875414,0.00020381818,0.00039016342,0.0007721713],"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":[0.000026610463,0.000004104852,0.00020010355,0.000007446549,8.9281707e-7,0.000028322964,0.000012729118,0.000012148687,0.9990663,0.00009172949,0.000018066723,0.0005316163],"study_design_scores_gemma":[0.000023096207,0.00015582828,0.018006653,0.000014364222,0.000013420554,0.00046053817,0.00008137173,0.0016049531,0.9731717,0.00008558578,0.006374587,0.000007839137],"about_ca_topic_score_codex":0.0005706158,"about_ca_topic_score_gemma":0.0013495454,"teacher_disagreement_score":0.0019233084,"about_ca_system_score_codex":0.0002789305,"about_ca_system_score_gemma":0.000084637984,"threshold_uncertainty_score":0.0064341426},"labels":[],"label_agreement":null},{"id":"W4388302377","doi":"10.1002/oby.23928","title":"Diazoxide choline extended‐release tablet in people with <scp>Prader‐Willi</scp> syndrome: results from long‐term open‐label study","year":2023,"lang":"en","type":"article","venue":"Obesity","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":22,"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":"Eunice Kennedy Shriver National Institute of Child Health and Human Development; National Heart, Lung, and Blood Institute; National Institute of Child Health and Human Development; School of Medicine, Indiana University; University of California, Irvine; York University; Queen Mary University of London; National Institutes of Health; Barts Health NHS Trust; Alder Hey Children's NHS Foundation Trust; Children's Hospital Colorado","keywords":"Diazoxide; Open label; Choline; Pharmacology; Chemistry; Medicine; Endocrinology; Insulin","score_opus":0.018834351259318843,"score_gpt":0.2702023846741543,"score_spread":0.2513680334148355,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4388302377","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9968393,0.002363626,0.000111314934,0.000044697576,0.000016105452,0.00019718506,0.0001557625,0.000008288518,0.0002635914],"genre_scores_gemma":[0.99732375,0.0013992592,0.00032843996,0.000112974165,0.000038996386,0.00016065153,0.00024017591,0.0000025923998,0.00039303984],"study_design_codex":"randomized_trial","study_design_gemma":"observational","domain_scores_codex":[0.9996816,0.00013744361,0.00004442829,0.000045292465,0.000062197134,0.000028979272],"domain_scores_gemma":[0.9993017,0.00018799334,0.00025945826,0.000044122524,0.00008131294,0.00012543351],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0011811688,0.00033752059,0.001067468,0.00018356093,0.00022192979,0.0002977858,0.00023613987,0.00047110545,0.0012242805],"category_scores_gemma":[0.0010145404,0.00016967717,0.0007596402,0.00019604502,0.00022576113,0.0003443571,0.00016186852,0.00068092055,0.00017482166],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.5489325,0.039523877,0.07618868,0.0034153685,0.0055153538,0.0007168751,0.0008352203,0.00073358207,0.06000273,0.00007885795,0.0012101692,0.26284677],"study_design_scores_gemma":[0.13534096,0.58285874,0.26825622,0.00021175643,0.0025890542,0.00065375346,0.0003108068,0.0011195752,0.005396963,0.000067546076,0.0031377685,0.00005686892],"about_ca_topic_score_codex":0.0009040452,"about_ca_topic_score_gemma":0.0018278637,"teacher_disagreement_score":0.0012242805,"about_ca_system_score_codex":0.00025219852,"about_ca_system_score_gemma":0.0003407086,"threshold_uncertainty_score":0.006246686},"labels":[],"label_agreement":null},{"id":"W4388461661","doi":"10.1016/j.gim.2023.101023","title":"Biallelic CRELD1 variants cause a multisystem syndrome, including neurodevelopmental phenotypes, cardiac dysrhythmias, and frequent infections","year":2023,"lang":"en","type":"article","venue":"Genetics in Medicine","topic":"Genetic Syndromes and Imprinting","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":"St. Thomas Hospital; Hospital for Sick Children","funders":"Yale Center for Clinical Investigation, Yale School of Medicine; Eunice Kennedy Shriver National Institute of Child Health and Human Development; National Institute of Neurological Disorders and Stroke; National Eye Institute; National Heart, Lung, and Blood Institute; Perelman School of Medicine, University of Pennsylvania; Intellectual and Developmental Disabilities Research Center; Horizon 2020; National Human Genome Research Institute; Epilepsy Society; Deutsche Forschungsgemeinschaft; European Commission; Broad Institute; National Institute for Health and Care Research; Institute for Translational Medicine and Therapeutics; HORIZON EUROPE Framework Programme; Yale New Haven Hospital; Cancer Research UK; Wellcome Trust; University of Pennsylvania; National Center for Advancing Translational Sciences; Medical Research Council; Hartwell Foundation; Health Research Institute, University of Limerick; Horizon 2020 Framework Programme; Children's Hospital of Philadelphia; Yale University; National Institutes of Health; U.S. Department of Health and Human Services","keywords":"Missense mutation; Phenotype; Frameshift mutation; Gene knockdown; Biology; Exome sequencing; Neurodevelopmental disorder; Allele; Genetics; Gene","score_opus":0.03252461494893546,"score_gpt":0.29081579455699774,"score_spread":0.2582911796080623,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4388461661","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9719982,0.0025203018,0.010246998,0.0010638828,0.0002028685,0.000088319306,0.0038759918,0.00078673934,0.009216758],"genre_scores_gemma":[0.9919674,0.0003886089,0.0035890818,0.00025994983,0.00006171624,0.000022327342,0.0006842576,0.0001352347,0.0028914097],"study_design_codex":"bench_or_experimental","study_design_gemma":"case_report","domain_scores_codex":[0.9995389,0.000048781127,0.000055698958,0.00013538546,0.00015094182,0.000070406255],"domain_scores_gemma":[0.99903476,0.0002713977,0.00033756284,0.00006780551,0.00006734569,0.00022120227],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0002507023,0.0017559838,0.0006440915,0.0020054777,0.00058272725,0.0006321631,0.0006140554,0.0016215575,0.006467413],"category_scores_gemma":[0.0011251149,0.00034135475,0.0004718551,0.0010433209,0.00068378187,0.00039971594,0.0009596486,0.0007517518,0.0011825333],"study_design_candidate":"case_report","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0018225037,0.00021081849,0.0644481,0.00037827314,0.0005248298,0.10121213,0.00064985355,0.0009791333,0.7879899,0.0033835345,0.0031340856,0.03526684],"study_design_scores_gemma":[0.00026404267,0.00043082543,0.20950945,0.00032103164,0.0009787304,0.49058908,0.0008218249,0.0041795396,0.26178744,0.004596847,0.026321292,0.0002000312],"about_ca_topic_score_codex":0.00090650446,"about_ca_topic_score_gemma":0.0015998724,"teacher_disagreement_score":0.006467413,"about_ca_system_score_codex":0.00032023995,"about_ca_system_score_gemma":0.00030320341,"threshold_uncertainty_score":0.021635592},"labels":[],"label_agreement":null},{"id":"W4389024517","doi":"10.1096/fasebj.30.1_supplement.802.8","title":"Human growth gene family chromosomal architecture is affected by maternal obesity, gestational diabetes and insulin treatment","year":2016,"lang":"en","type":"article","venue":"The FASEB Journal","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":0,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":true,"ca_institutions":"University of Manitoba","funders":"Canadian Institutes of Health Research","keywords":"Endocrinology; Internal medicine; Biology; Insulin resistance; Locus (genetics); Chromatin; Gestational diabetes; Chromatin immunoprecipitation; Gene; Gene expression; Insulin; Promoter; Pregnancy; Genetics; Gestation; Medicine","score_opus":0.00672912589708902,"score_gpt":0.21356819966136048,"score_spread":0.20683907376427146,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4389024517","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9979875,0.00032775995,0.00031405478,0.000064359185,0.0000075416674,0.000003257301,0.0002907317,0.00002057455,0.0009841818],"genre_scores_gemma":[0.99829334,0.00017847522,0.00022168344,0.000025504964,0.0000061207884,0.000009201054,0.00036334142,0.000011137556,0.00089120335],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9998872,0.00002872428,0.0000061517267,0.000038414175,0.000021389682,0.000018037048],"domain_scores_gemma":[0.99971145,0.00006047789,0.00012838174,0.000020411024,0.000018659268,0.000060626764],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.000095392716,0.00033302468,0.00015740024,0.00060275267,0.0001707788,0.00016758898,0.0001233674,0.00018448757,0.0032710074],"category_scores_gemma":[0.00033384893,0.00012851869,0.00015909536,0.00043133335,0.0001534665,0.00006923517,0.00012658509,0.00021118468,0.00029371117],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.004584071,0.0001565453,0.45342988,0.000055600543,0.0001984598,0.0032474718,0.00036580008,0.00024109316,0.5173352,0.0002885397,0.00075549335,0.01934189],"study_design_scores_gemma":[0.000016717973,0.00014797195,0.98976105,0.000005195604,0.000035125206,0.0026825578,0.000054865657,0.00023295333,0.005926096,0.00006114732,0.0010720723,0.000004292524],"about_ca_topic_score_codex":0.0017687381,"about_ca_topic_score_gemma":0.001371089,"teacher_disagreement_score":0.0032710074,"about_ca_system_score_codex":0.0001585166,"about_ca_system_score_gemma":0.00012121469,"threshold_uncertainty_score":0.010942638},"labels":[],"label_agreement":null},{"id":"W4389341139","doi":"10.5772/intechopen.113912","title":"Founder Effect: Breeding a Dog for the Elderly Gentleman Reveals an Animal Model of a Human Genetic Disorder","year":2023,"lang":"en","type":"book-chapter","venue":"Genetics.","topic":"Genetic Syndromes and Imprinting","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":"Hospital for Sick Children; University of Toronto","funders":"","keywords":"Breed; Biology; Population; Genetics; Population bottleneck; Allele; Genotyping; Founder effect; Mutation; Gene; Genotype; Demography; Microsatellite; Haplotype","score_opus":0.03272385351567018,"score_gpt":0.283637738525617,"score_spread":0.2509138850099468,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4389341139","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":[0.006652747,0.7181621,0.014550391,0.011573852,0.0112360325,0.00006178668,0.0002951425,0.00057957845,0.23688835],"genre_scores_gemma":[0.021864092,0.35775203,0.02097298,0.012495951,0.0038698763,0.000111772446,0.00045947218,0.00037185068,0.58210194],"study_design_codex":"design_other","study_design_gemma":"observational","domain_scores_codex":[0.99988425,0.000022428358,0.000006428909,0.000031503823,0.000047866146,0.000007511613],"domain_scores_gemma":[0.9998795,0.00007580927,0.000009059023,0.000007907233,0.000014134789,0.000013597909],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00029604262,0.0005004386,0.00043550247,0.00074071944,0.00028513683,0.00088421244,0.00058677234,0.001107139,0.010882476],"category_scores_gemma":[0.00029050102,0.00016900209,0.000277198,0.00044026432,0.0009010324,0.0011338941,0.00061140006,0.0018132101,0.0061494587],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00011217494,0.00012379023,0.00037935155,0.0015945456,0.000032798802,0.001878283,0.0007614159,0.00035996357,0.019920936,0.08597151,0.38016343,0.5087018],"study_design_scores_gemma":[0.000004214511,0.000039318475,0.00034771013,0.00018199797,0.000009879757,0.002672039,0.00003799048,0.00008096407,0.00075168017,0.005406559,0.9904614,0.0000061547626],"about_ca_topic_score_codex":0.00049083494,"about_ca_topic_score_gemma":0.0014991037,"teacher_disagreement_score":0.010882476,"about_ca_system_score_codex":0.0004643865,"about_ca_system_score_gemma":0.00026981183,"threshold_uncertainty_score":0.036405504},"labels":[],"label_agreement":null},{"id":"W4390222174","doi":"10.1016/j.nsa.2023.103880","title":"Using eye-tracking to measure hyperphagia in Prader-Willi Syndrome","year":2023,"lang":"en","type":"article","venue":"Neuroscience Applied","topic":"Genetic Syndromes and Imprinting","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":"SickKids Foundation; University of Toronto","funders":"","keywords":"Measure (data warehouse); Tracking (education); Psychology; Artificial intelligence; Computer science; Data mining","score_opus":0.05030297828866744,"score_gpt":0.3089278877563804,"score_spread":0.258624909467713,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4390222174","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9886972,0.0011243228,0.007823778,0.000058508675,0.000036563826,0.000060065835,0.00026457137,0.00008011081,0.0018549184],"genre_scores_gemma":[0.9920109,0.00059826695,0.0062196343,0.00011486485,0.000011190623,0.000062131745,0.00011837674,0.000021093389,0.0008435119],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9995235,0.00018239765,0.000044922006,0.00010314424,0.000105512925,0.00004051609],"domain_scores_gemma":[0.9994709,0.00025547316,0.000097428194,0.000033783923,0.000081002145,0.000061432715],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0005526082,0.00039275084,0.0003342174,0.00086645683,0.00020747143,0.0003386185,0.00019778813,0.00053150684,0.00049528736],"category_scores_gemma":[0.0014908101,0.00017690027,0.00018345508,0.00041629025,0.0002715533,0.0003166986,0.0003764261,0.00064227585,0.00016090443],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0020709168,0.00031280154,0.3658711,0.00020765343,0.00022835234,0.0016429942,0.00057118176,0.0015119807,0.5598071,0.00022472635,0.00038007493,0.06717116],"study_design_scores_gemma":[0.000060833037,0.0017036967,0.87772524,0.00003552409,0.00014544459,0.005563271,0.00030990117,0.006238244,0.10712325,0.00021539537,0.00082299684,0.0000561849],"about_ca_topic_score_codex":0.003251595,"about_ca_topic_score_gemma":0.004247339,"teacher_disagreement_score":0.003251595,"about_ca_system_score_codex":0.00027808212,"about_ca_system_score_gemma":0.00019749718,"threshold_uncertainty_score":0.006465316},"labels":[],"label_agreement":null},{"id":"W4390223190","doi":"10.1016/j.nsa.2023.103883","title":"Exploring the role of social cognition in autism behaviours within Prader-Willi Syndrome","year":2023,"lang":"en","type":"article","venue":"Neuroscience Applied","topic":"Genetic Syndromes and Imprinting","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":"SickKids Foundation; University of Toronto","funders":"","keywords":"Autism; Psychology; Cognition; Social cognition; Developmental psychology; Cognitive psychology; Neuroscience","score_opus":0.041965605319048575,"score_gpt":0.2557095995503657,"score_spread":0.21374399423131712,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4390223190","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99433374,0.001125594,0.00097153836,0.00045247245,0.00001011257,0.000007184103,0.000038324226,0.00000758574,0.0030534524],"genre_scores_gemma":[0.99786335,0.0006673797,0.000886212,0.000039161605,0.000007301821,0.000008736702,0.000017860288,0.000002563119,0.0005074715],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.99986315,0.000054545857,0.000006946138,0.000019155908,0.00003072699,0.000025454048],"domain_scores_gemma":[0.99980515,0.00009590377,0.00004092788,0.000011800984,0.000018738861,0.000027560292],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00038555788,0.00041893864,0.00017596994,0.00055075233,0.00031809023,0.000492214,0.000397425,0.00032852945,0.001132521],"category_scores_gemma":[0.0006280647,0.000114113565,0.00016929401,0.00022499355,0.0013829092,0.00041938678,0.0006111821,0.0006141906,0.00007919315],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.001799582,0.0005497983,0.20047191,0.0005832431,0.00018912535,0.015404705,0.0067272987,0.0034144628,0.6360957,0.04039567,0.0005122808,0.09385628],"study_design_scores_gemma":[0.000079089754,0.001230279,0.87017006,0.00012559134,0.00015208007,0.007597354,0.009113313,0.005518812,0.07463518,0.0258273,0.0054949536,0.000056044486],"about_ca_topic_score_codex":0.0039493553,"about_ca_topic_score_gemma":0.004134948,"teacher_disagreement_score":0.0039493553,"about_ca_system_score_codex":0.0005432177,"about_ca_system_score_gemma":0.00068607304,"threshold_uncertainty_score":0.007852733},"labels":[],"label_agreement":null},{"id":"W4390267137","doi":"10.7554/elife.92942.1.sa1","title":"Reviewer #1 (Public Review): BMP signalling facilitates transit amplification in the developing chick and human cerebellum","year":2023,"lang":"en","type":"peer-review","venue":"","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":0,"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; Menzies Centre for Australian Studies, King's College London, University of London; University of East Anglia; King's College London; Queen Mary University of London","keywords":"Cell biology; Granule cell; Cerebellum; Biology; Bone morphogenetic protein; Sonic hedgehog; Cerebellar cortex; Granule (geology); Signalling; Neurogenesis; BMPR2; Progenitor cell; Neuroscience; Dentate gyrus; Signal transduction; Stem cell; Genetics; Central nervous system","score_opus":0.060833655691213434,"score_gpt":0.3158129804725798,"score_spread":0.2549793247813663,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4390267137","genre_codex":"editorial","genre_gemma":"commentary","domain_codex":null,"domain_gemma":"evaluation","model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"commentary","genre_consensus":null,"domain_candidate":"evaluation","domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.00041288594,0.0168497,0.0009923618,0.35208303,0.62077844,0.0010706185,0.0023647451,0.0005115013,0.004936655],"genre_scores_gemma":[0.008375222,0.022730872,0.0019690548,0.46732,0.445303,0.0045599346,0.002524819,0.0008001907,0.04641696],"study_design_codex":"not_applicable","study_design_gemma":"not_applicable","domain_scores_codex":[0.978114,0.0061995434,0.0036845345,0.0026012387,0.008225203,0.0011753635],"domain_scores_gemma":[0.74584264,0.026338281,0.015561759,0.00658464,0.19569902,0.009973649],"candidate_categories":["metaresearch"],"consensus_categories":[],"category_scores_codex":[0.033428237,0.0016016465,0.0033613993,0.0039064502,0.0027523167,0.008700911,0.0058752396,0.02138444,0.059519522],"category_scores_gemma":[0.17751874,0.0014210342,0.0035566755,0.0022052694,0.0025133467,0.0043529067,0.0040907227,0.0075776717,0.031003233],"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":[0.000066881104,0.00000636108,0.00012578465,0.0016279334,0.000032148015,0.000053488762,0.000031970223,0.000019160114,0.00008255384,0.000101853315,0.9913238,0.006527937],"study_design_scores_gemma":[0.000364001,0.00009900236,0.0022574377,0.0051917722,0.00021431732,0.0004403234,0.00019408249,0.00020337419,0.00040603158,0.0010872298,0.98944235,0.00010014195],"about_ca_topic_score_codex":0.00354215,"about_ca_topic_score_gemma":0.0052104876,"teacher_disagreement_score":0.96657175,"about_ca_system_score_codex":0.007430285,"about_ca_system_score_gemma":0.013009367,"threshold_uncertainty_score":0.19911265},"labels":[],"label_agreement":null},{"id":"W4391069390","doi":"10.1016/b978-0-12-816478-5.00056-x","title":"Endocrinologic and Growth Cases: Short Stature","year":2024,"lang":"en","type":"book-chapter","venue":"Elsevier eBooks","topic":"Genetic Syndromes and Imprinting","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":"SickKids Foundation; Hospital for Sick Children; University of Toronto","funders":"","keywords":"Short stature; Uniparental disomy; Small for gestational age; Pediatrics; Biology; Medicine; Chromosome; Genetics; Gestational age; Pregnancy; Karyotype","score_opus":0.012741959985496066,"score_gpt":0.23816888732993757,"score_spread":0.2254269273444415,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4391069390","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":[0.010519953,0.045263305,0.0012841569,0.004898472,0.002417375,0.00003206098,0.00030449408,0.00020296856,0.93507725],"genre_scores_gemma":[0.09626042,0.045716166,0.0029009138,0.003315672,0.004209613,0.00007144305,0.0008136857,0.00013926045,0.84657276],"study_design_codex":"design_other","study_design_gemma":"case_report","domain_scores_codex":[0.99994445,0.000008444013,0.0000042341776,0.000008000175,0.000025986827,0.000008840392],"domain_scores_gemma":[0.99993086,0.000037626574,0.000003687065,0.0000045214133,0.000005272076,0.00001808141],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.000102449114,0.0005115287,0.00023891295,0.0009876658,0.00031806686,0.00050805457,0.0005542326,0.00087204756,0.038780935],"category_scores_gemma":[0.00026219006,0.00019629828,0.00015963678,0.0005931875,0.00043141042,0.000451492,0.0005957471,0.0010579419,0.010206993],"study_design_candidate":"case_report","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00019795935,0.00026014354,0.004439021,0.00033897633,0.000032196866,0.063337386,0.00062160386,0.001257485,0.0061619477,0.04571452,0.33686167,0.5407771],"study_design_scores_gemma":[0.000037154787,0.00009028411,0.007428358,0.0002897966,0.000015744876,0.073859155,0.00027092246,0.0003692633,0.0005569374,0.019273518,0.8977927,0.000016119115],"about_ca_topic_score_codex":0.0015818599,"about_ca_topic_score_gemma":0.0044132173,"teacher_disagreement_score":0.038780935,"about_ca_system_score_codex":0.00022790658,"about_ca_system_score_gemma":0.00017101572,"threshold_uncertainty_score":0.12973511},"labels":[],"label_agreement":null},{"id":"W4391321767","doi":"10.1177/10497323231225412","title":"Mothering a Child With Complexity and Rarity: A Narrative Inquiry Exploring Prader-Willi Syndrome","year":2024,"lang":"en","type":"article","venue":"Qualitative Health Research","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":7,"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 Victoria; University of Calgary; Mount Royal University","funders":"Mount Royal University","keywords":"Narrative; Narrative inquiry; Normative; Psychology; Mental health; Developmental psychology; Quality of life (healthcare); Everyday life; Psychotherapist","score_opus":0.5099474836932916,"score_gpt":0.5163274933563686,"score_spread":0.0063800096630770575,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4391321767","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9788411,0.0023670304,0.0038528314,0.006093763,0.000110250054,0.0002187678,0.00011526241,0.000028374676,0.0083725825],"genre_scores_gemma":[0.9907184,0.002482805,0.0030562447,0.0006732008,0.000035268393,0.00019377907,0.000055335848,0.000033334934,0.0027515977],"study_design_codex":"qualitative","study_design_gemma":"qualitative","domain_scores_codex":[0.9942731,0.004475797,0.00017895359,0.00028789177,0.00033074923,0.00045340354],"domain_scores_gemma":[0.99096304,0.0067725964,0.000909497,0.00025021378,0.0003663108,0.00073838624],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0062469193,0.0009264611,0.00093885954,0.0014381298,0.009866817,0.0064586652,0.0024182599,0.0022866693,0.0016760948],"category_scores_gemma":[0.0135968765,0.0008361855,0.00045719428,0.0011882931,0.012382135,0.006706039,0.008793889,0.004195808,0.00031422876],"study_design_candidate":"qualitative","study_design_consensus":"qualitative","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.000012149489,0.000009542584,0.0007219808,0.000049661827,0.0000023100763,0.0019911504,0.99460876,0.000022506756,0.00024826342,0.0010001439,0.00025154444,0.0010818662],"study_design_scores_gemma":[0.0000024752494,0.000020701898,0.00057000224,0.000110507724,0.000004262283,0.0015973375,0.98996454,0.000057237667,0.000158082,0.00048085273,0.007024151,0.000009846853],"about_ca_topic_score_codex":0.007315517,"about_ca_topic_score_gemma":0.015580342,"teacher_disagreement_score":0.009866817,"about_ca_system_score_codex":0.005036281,"about_ca_system_score_gemma":0.0036151614,"threshold_uncertainty_score":0.036540926},"labels":[],"label_agreement":null},{"id":"W4391771437","doi":"10.1101/2024.02.12.24302716","title":"Fine-mapping genomic loci refines bipolar disorder risk genes","year":2024,"lang":"en","type":"preprint","venue":"medRxiv","topic":"Genetic Syndromes and Imprinting","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; Centre for Addiction and Mental Health; Dalhousie University","funders":"National Health and Medical Research Council; Canadian Institutes of Health Research; NIHR Maudsley Biomedical Research Centre; Stanley Center for Psychiatric Research, Broad Institute; National Institutes of Health; Vetenskapsrådet; National Institute of Mental Health; Stockholms Läns Landsting; Instituto de Salud Carlos III; Universitat de Barcelona; National Research Foundation; Medical Research Council; Università di Bologna; Department of Health and Social Care; National Research Foundation of Korea; King's College London; Departament d'Innovació, Universitats i Empresa, Generalitat de Catalunya; Victoria General Hospital Foundation; Generalitat de Catalunya; European Regional Development Fund; Bundesministerium für Bildung und Forschung; National Institute for Health and Care Research; Karl-Franzens-Universität Graz; Japan Agency for Medical Research and Development; Deutsche Forschungsgemeinschaft; Japan Society for the Promotion of Science; Medizinische Universität Graz; Amt der Steiermärkischen Landesregierung; GlaxoSmithKline; Centres de Recerca de Catalunya; Michael Smith Health Research BC; Maudsley Charity; Wellcome Trust; Ministerio de Ciencia e Innovación; European Commission; University of California, Irvine; Broad Institute; Ministerio de Economía y Competitividad; University of Pittsburgh; Centro de Investigación Biomédica en Red de Salud Mental; National Alliance for Research on Schizophrenia and Depression; U.S. Department of Health and Human Services","keywords":"Biology; Genetics; Single-nucleotide polymorphism; Computational biology; Exome sequencing; Gene; Epigenomics; Genome; Genome-wide association study; Phenotype; DNA methylation","score_opus":0.012729237597689158,"score_gpt":0.24100159496176624,"score_spread":0.22827235736407708,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4391771437","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.69302887,0.006986255,0.21120831,0.0013579543,0.0003735429,0.00025887074,0.060672633,0.01159415,0.014519462],"genre_scores_gemma":[0.83272773,0.0019421413,0.12504257,0.0008656061,0.00011648887,0.0001866879,0.030501151,0.0029501647,0.005667426],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9996568,0.000048005324,0.000016732438,0.00015660263,0.00008158445,0.000040295974],"domain_scores_gemma":[0.99961865,0.0001552539,0.000071342896,0.00006587005,0.00004391868,0.00004486647],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0009581895,0.0006577987,0.00065810606,0.0012394092,0.00046391797,0.0009734259,0.00039037326,0.000371869,0.009858491],"category_scores_gemma":[0.0016737811,0.0003820405,0.00089651847,0.0007819318,0.00020003844,0.00022021252,0.00065968884,0.0008197321,0.0026940294],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0018808673,0.00017108246,0.1570919,0.0013013938,0.0014922225,0.0018146108,0.00058175327,0.021512887,0.54979455,0.0065805484,0.037443887,0.22033428],"study_design_scores_gemma":[0.001423363,0.00051902316,0.5625604,0.0007576147,0.0028334232,0.0049675703,0.00035982142,0.087589756,0.18545769,0.024855943,0.12837586,0.00029968112],"about_ca_topic_score_codex":0.0041539827,"about_ca_topic_score_gemma":0.009028096,"teacher_disagreement_score":0.009858491,"about_ca_system_score_codex":0.000353173,"about_ca_system_score_gemma":0.00048343942,"threshold_uncertainty_score":0.032979906},"labels":[],"label_agreement":null},{"id":"W4392049994","doi":"10.7554/elife.94502","title":"Post-fertilization transcription initiation in an ancestral LTR retrotransposon drives lineage-specific genomic imprinting of ZDBF2","year":2024,"lang":"en","type":"article","venue":"eLife","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":1,"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":"NODAI Genome Research Center, Tokyo University of Agriculture; Canadian Institutes of Health Research; Mitsubishi Foundation; Japan Society for the Promotion of Science; Ministry of Education, Culture, Sports, Science and Technology; Tokyo University of Agriculture; Takeda Science Foundation","keywords":"Retrotransposon; Genomic imprinting; Imprinting (psychology); Biology; Genetics; Lineage (genetic); Gene; Computational biology; Genome; Transposable element; DNA methylation; Gene expression","score_opus":0.0193719705543862,"score_gpt":0.2651506837435218,"score_spread":0.2457787131891356,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4392049994","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9953746,0.00044568762,0.0024771313,0.00003359605,0.000009085847,0.000009028846,0.00017403183,0.000059278984,0.0014174943],"genre_scores_gemma":[0.99607986,0.00017583335,0.0011511511,0.000024630846,0.0000037248278,0.000005539005,0.0003376871,0.00001800971,0.0022036564],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9999044,0.000012964815,0.0000058914534,0.000032815737,0.000020939511,0.000022966082],"domain_scores_gemma":[0.99992824,0.000017181404,0.000022923827,0.0000107985215,0.000006539068,0.000014321853],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00011533333,0.00015100765,0.00009600459,0.00016880463,0.00013140078,0.0001793957,0.00015452935,0.00015861217,0.0010497286],"category_scores_gemma":[0.0001239875,0.00013733919,0.0001529196,0.00008963668,0.00015154613,0.00009886062,0.00021730644,0.00028696732,0.00045787642],"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":[0.000030471861,0.0000028349516,0.00048673537,0.000008267787,9.895457e-7,0.00005040503,0.000028082703,0.0000161638,0.9982292,0.00011106808,0.0000134923075,0.0010223609],"study_design_scores_gemma":[0.000026372352,0.00017574955,0.044181116,0.00001531006,0.000019176563,0.0008405923,0.00013691383,0.0016386769,0.94428813,0.00010021025,0.008568707,0.000009153186],"about_ca_topic_score_codex":0.0006981059,"about_ca_topic_score_gemma":0.0018412601,"teacher_disagreement_score":0.0010497286,"about_ca_system_score_codex":0.00024314522,"about_ca_system_score_gemma":0.00012024375,"threshold_uncertainty_score":0.0035116673},"labels":[],"label_agreement":null},{"id":"W4392080976","doi":"10.7554/elife.94502.1","title":"Post-fertilization transcription initiation in an ancestral LTR retrotransposon drives lineage-specific genomic imprinting of ZDBF2","year":2024,"lang":"en","type":"preprint","venue":"","topic":"Genetic Syndromes and Imprinting","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":"University of British Columbia","funders":"","keywords":"Genomic imprinting; Biology; Retrotransposon; DNA methylation; Genetics; Imprinting (psychology); Gene; Genome; Transposable element; Gene expression","score_opus":0.024138101324923143,"score_gpt":0.27022452178437434,"score_spread":0.2460864204594512,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4392080976","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9958895,0.0004202879,0.0022779063,0.000033522545,0.000011145089,0.000008607971,0.00029861936,0.00005538256,0.0010049898],"genre_scores_gemma":[0.9952543,0.00013613932,0.0012263528,0.000030278798,0.0000045080155,0.000006816073,0.0005440857,0.000022175376,0.0027754004],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9999137,0.000009710769,0.000004484084,0.000033720524,0.000017171784,0.00002113044],"domain_scores_gemma":[0.9999397,0.000014340221,0.000019515594,0.0000072713883,0.0000053032873,0.000013895015],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00007993091,0.00015299254,0.00009570177,0.00015966922,0.00011768791,0.00018096493,0.00012637523,0.00017437682,0.0014150222],"category_scores_gemma":[0.000086723965,0.00012042575,0.00013673079,0.00008097359,0.00012579058,0.00008192941,0.00018932257,0.0002909584,0.00055775914],"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":[0.000024139279,0.0000024310618,0.0002183238,0.000005902359,6.220643e-7,0.000025362873,0.000011885526,0.000009552137,0.9991486,0.000055643664,0.000011293414,0.00048615562],"study_design_scores_gemma":[0.00001901052,0.00016935621,0.031480398,0.000011772287,0.000011923079,0.0006248153,0.0001056484,0.0017593624,0.95923555,0.000083549974,0.0064907996,0.00000778921],"about_ca_topic_score_codex":0.0005073062,"about_ca_topic_score_gemma":0.0012029754,"teacher_disagreement_score":0.0014150222,"about_ca_system_score_codex":0.0002038862,"about_ca_system_score_gemma":0.00007583632,"threshold_uncertainty_score":0.0047336817},"labels":[],"label_agreement":null},{"id":"W4392131917","doi":"10.1002/mgg3.2402","title":"A homozygous stop codon in <i>HORMAD2</i> in a patient with recurrent digynic triploid miscarriage","year":2024,"lang":"en","type":"article","venue":"Molecular Genetics & Genomic Medicine","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":2,"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; Hospital for Sick Children; McGill University; McGill University Health Centre","funders":"Canadian Institutes of Health Research; McGill University Health Centre; Génome Québec; McGill University","keywords":"Biology; Genetics; Sanger sequencing; Meiosis; SNP array; Exome sequencing; Aneuploidy; Single-nucleotide polymorphism; Gene; Genotype; Chromosome; Phenotype; Mutation","score_opus":0.006433787523581298,"score_gpt":0.23030253521634822,"score_spread":0.22386874769276693,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4392131917","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99411315,0.0011050557,0.0009534414,0.0010385007,0.000084897285,0.000044393855,0.00021456934,0.00007323051,0.002372851],"genre_scores_gemma":[0.99861336,0.00021595422,0.00044729625,0.00021411963,0.000074575655,0.000008470477,0.00008217471,0.00001134219,0.0003327355],"study_design_codex":"case_report","study_design_gemma":"case_report","domain_scores_codex":[0.99970347,0.000026558328,0.000034154553,0.00011661528,0.00005018173,0.00006898587],"domain_scores_gemma":[0.9993562,0.00021180512,0.00014468227,0.000032797176,0.000039486546,0.00021516456],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00026102204,0.0012129275,0.0004890486,0.0016826103,0.0010196277,0.00057665596,0.00071311067,0.0021965005,0.0019223052],"category_scores_gemma":[0.0015082648,0.00043432342,0.00051782175,0.0007525259,0.0008059722,0.0004353904,0.0005952326,0.0009963356,0.00046752163],"study_design_candidate":"case_report","study_design_consensus":"case_report","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00010243199,0.000029385796,0.026335223,0.000031210042,0.000020555737,0.96169007,0.0004213265,0.00012833303,0.0081138415,0.00021296463,0.0003849207,0.0025297543],"study_design_scores_gemma":[0.000017776207,0.00013564363,0.020644674,0.000016043481,0.000030917134,0.97594213,0.00013279608,0.00026313265,0.0018643755,0.0001583666,0.00077718764,0.000016974245],"about_ca_topic_score_codex":0.0018210515,"about_ca_topic_score_gemma":0.0013379807,"teacher_disagreement_score":0.0021965005,"about_ca_system_score_codex":0.00060218305,"about_ca_system_score_gemma":0.00031596693,"threshold_uncertainty_score":0.006430745},"labels":[],"label_agreement":null},{"id":"W4392361808","doi":"10.5664/jcsm.11078","title":"14 and 6 Hz like spike wave activity is a common finding in young patients with Prader–Willi syndrome","year":2024,"lang":"en","type":"article","venue":"Journal of Clinical Sleep Medicine","topic":"Genetic Syndromes and Imprinting","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":"SickKids Foundation; Hospital for Sick Children; University of Toronto","funders":"","keywords":"Medicine; Spike (software development); Audiology; Electroencephalography; Internal medicine; Psychiatry; Pediatrics","score_opus":0.028019368282374633,"score_gpt":0.33454208332579044,"score_spread":0.3065227150434158,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4392361808","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99669325,0.00038488346,0.00048054763,0.00010428929,0.00003895817,0.000019269479,0.00022703945,0.000054455126,0.0019972355],"genre_scores_gemma":[0.998323,0.00025626743,0.00031262738,0.000101326885,0.00003895123,0.000010371924,0.00024395026,0.000013403566,0.00070006185],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99978954,0.00003068757,0.000031263386,0.000048891598,0.000061247054,0.000038414524],"domain_scores_gemma":[0.99905664,0.0002975265,0.00033257384,0.000043765667,0.0000745697,0.00019494463],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00015117998,0.00061410514,0.00047222,0.0010895815,0.00026874716,0.0002959365,0.00039983733,0.0007480126,0.003339807],"category_scores_gemma":[0.0015419627,0.00022284195,0.0002620841,0.00052360195,0.00031224944,0.0002725441,0.00032133667,0.00049148826,0.0004971424],"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":[0.00084780366,0.00023303131,0.6854005,0.00014494048,0.00014051893,0.19987534,0.000923482,0.00014775521,0.095825695,0.00031991568,0.0009807912,0.015160237],"study_design_scores_gemma":[0.000019606023,0.00043538373,0.78265417,0.000014055679,0.00005782829,0.21332493,0.00035964404,0.0002307097,0.0020583358,0.00012398328,0.00069988216,0.000021448113],"about_ca_topic_score_codex":0.001192752,"about_ca_topic_score_gemma":0.0015207243,"teacher_disagreement_score":0.003339807,"about_ca_system_score_codex":0.0000899234,"about_ca_system_score_gemma":0.00019951482,"threshold_uncertainty_score":0.011172712},"labels":[],"label_agreement":null},{"id":"W4392466924","doi":"10.3389/fcell.2024.1369751","title":"Roles of endogenous retroviral elements in the establishment and maintenance of imprinted gene expression","year":2024,"lang":"en","type":"article","venue":"Frontiers in Cell and Developmental Biology","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":7,"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":"Canadian Institutes of Health Research","keywords":"Genomic imprinting; Biology; Epigenetics; Genetics; Gene silencing; DNA methylation; Histone; Imprinting (psychology); Endogenous retrovirus; Gene; Germline; Regulation of gene expression; Gene expression; Genome","score_opus":0.007685880341422367,"score_gpt":0.2102407274092707,"score_spread":0.20255484706784832,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4392466924","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":[0.3883914,0.5319089,0.04809778,0.0007499819,0.0005389176,0.00006473852,0.00083341607,0.0005455542,0.028869323],"genre_scores_gemma":[0.8661919,0.114709474,0.00819361,0.00026902847,0.00024088573,0.000040058087,0.0006873192,0.00006145564,0.0096062515],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99978775,0.00003102536,0.000019057965,0.00005545975,0.00007228922,0.000034326036],"domain_scores_gemma":[0.99988306,0.00003599719,0.000036063506,0.00001359727,0.00001450307,0.00001667171],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00029764842,0.00021127693,0.00019626123,0.00027743305,0.00014869309,0.0007117277,0.00025909426,0.00023077744,0.0008717481],"category_scores_gemma":[0.0002494874,0.00011653555,0.00024501228,0.00018939623,0.0004427527,0.00042512224,0.00030744338,0.00044477262,0.0004033304],"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":[0.0001978463,0.000056092867,0.006979719,0.0013092159,0.000097373464,0.0011797971,0.00023906208,0.00056185434,0.8206006,0.016041292,0.0005149489,0.1522223],"study_design_scores_gemma":[0.000033849854,0.0005840723,0.038380228,0.00043824414,0.00025752897,0.0059829997,0.00039147056,0.0024642197,0.77547264,0.007720151,0.16821443,0.000060231996],"about_ca_topic_score_codex":0.00020229621,"about_ca_topic_score_gemma":0.00029409872,"teacher_disagreement_score":0.0008717481,"about_ca_system_score_codex":0.0004304303,"about_ca_system_score_gemma":0.00022595796,"threshold_uncertainty_score":0.003123045},"labels":[],"label_agreement":null},{"id":"W4392564506","doi":"10.1101/gad.351238.123","title":"A maternal-effect<i>Padi6</i>variant causes nuclear and cytoplasmic abnormalities in oocytes, as well as failure of epigenetic reprogramming and zygotic genome activation in embryos","year":2024,"lang":"en","type":"article","venue":"Genes & Development","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":30,"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":"Biotechnology and Biological Sciences Research Council; Directorate for Biological Sciences; Medical Research Council; Associazione Italiana per la Ricerca sul Cancro; Medical Research Council Canada; Wellcome Trust","keywords":"Biology; Maternal to zygotic transition; Reprogramming; Genomic imprinting; Epigenetics; Zygote; DNA methylation; Genetics; Embryo; Oocyte; Imprinting (psychology); Gene; XIST; Cell biology; X-inactivation; Embryogenesis; Gene expression; X chromosome","score_opus":0.004728806393827955,"score_gpt":0.21467845354063803,"score_spread":0.20994964714681008,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4392564506","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9922312,0.0005231214,0.0039549763,0.00012114431,0.000050041566,0.00003405191,0.0009638118,0.0003631473,0.001758519],"genre_scores_gemma":[0.99450916,0.00031871698,0.00217434,0.0000601991,0.000022814686,0.00002646222,0.00075168157,0.0000977058,0.0020390737],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9997496,0.000026718051,0.000042281943,0.00008103409,0.00006727213,0.00003307676],"domain_scores_gemma":[0.99976224,0.000044384782,0.00008365371,0.00003226522,0.000008145245,0.000069341964],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00013783983,0.0006945226,0.0003176193,0.00042164564,0.00019768784,0.0002460878,0.000427704,0.00049885106,0.0021172885],"category_scores_gemma":[0.00020241487,0.0002584417,0.00038174674,0.00020810978,0.00042415154,0.000102722835,0.0003597845,0.00072011846,0.0006523781],"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":[0.000100371246,0.00002043419,0.000489267,0.000028331104,0.000011138893,0.0015524528,0.0000139162885,0.00006855438,0.9962798,0.00019670936,0.00006892844,0.0011701374],"study_design_scores_gemma":[0.00009376875,0.00040962404,0.029491372,0.000017332794,0.00007484793,0.02405137,0.00005968524,0.0018363735,0.93929785,0.00024682496,0.0044008316,0.000020259295],"about_ca_topic_score_codex":0.00047756723,"about_ca_topic_score_gemma":0.0006457797,"teacher_disagreement_score":0.0021172885,"about_ca_system_score_codex":0.0002054609,"about_ca_system_score_gemma":0.00015163011,"threshold_uncertainty_score":0.0070829988},"labels":[],"label_agreement":null},{"id":"W4392588876","doi":"10.1016/j.gimo.2024.101191","title":"P295: Expanding the prenatal phenotype of a rare syndrome due to variants in DPH1","year":2024,"lang":"en","type":"article","venue":"Genetics in Medicine Open","topic":"Genetic Syndromes and Imprinting","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":"University of Calgary; University of British Columbia","funders":"","keywords":"Phenotype; Genetics; Medicine; Biology; Gene","score_opus":0.021632580676808268,"score_gpt":0.3134563342496481,"score_spread":0.2918237535728398,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4392588876","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9818248,0.0010206279,0.005082559,0.0006147967,0.00013889457,0.00004419808,0.00048307423,0.00018132501,0.010609684],"genre_scores_gemma":[0.9940766,0.00040757612,0.0028199162,0.00014542509,0.000090728514,0.0000146808725,0.00019101061,0.000041989006,0.002212009],"study_design_codex":"case_report","study_design_gemma":"observational","domain_scores_codex":[0.9997739,0.000023605991,0.000019405394,0.00007124824,0.000071148024,0.000040610117],"domain_scores_gemma":[0.9996731,0.00012915871,0.00006464748,0.00001931795,0.000022804717,0.00009106466],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00010872271,0.0009086165,0.000291053,0.0008291625,0.0004505208,0.0003293856,0.0004671837,0.001151127,0.0042108265],"category_scores_gemma":[0.00085478165,0.00023969874,0.00025514554,0.00044266216,0.0006523755,0.00035397493,0.0008138558,0.0006476769,0.00078588905],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00008536629,0.000030632524,0.009356208,0.000060072198,0.000010281445,0.93696934,0.00025431282,0.00019304837,0.041871537,0.0009988024,0.00055767223,0.009612662],"study_design_scores_gemma":[0.000015216495,0.000068228124,0.016690653,0.000019960678,0.000021002568,0.9636403,0.00007098812,0.00052809395,0.015555219,0.00046232145,0.0029136094,0.0000145383865],"about_ca_topic_score_codex":0.00169885,"about_ca_topic_score_gemma":0.00123204,"teacher_disagreement_score":0.0042108265,"about_ca_system_score_codex":0.00024520015,"about_ca_system_score_gemma":0.00032508388,"threshold_uncertainty_score":0.014086604},"labels":[],"label_agreement":null},{"id":"W4392606465","doi":"10.1016/j.gimo.2024.101206","title":"P311: Use of a DNA methylation signature for the diagnosis of TET3-related Beck-Fahrner syndrome and expansion of its related phenotype","year":2024,"lang":"en","type":"article","venue":"Genetics in Medicine Open","topic":"Genetic Syndromes and Imprinting","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":"Hospital for Sick Children; Sunnybrook Health Science Centre; McMaster Children's Hospital; London Health Sciences Centre; McMaster University","funders":"","keywords":"DNA methylation; Phenotype; Signature (topology); Genetics; Methylation; Biology; Epigenetics; Computational biology; DNA; Mathematics; Gene","score_opus":0.033605987518793345,"score_gpt":0.30864572344937263,"score_spread":0.2750397359305793,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4392606465","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9846192,0.0013891002,0.0046066735,0.0014574593,0.00008257203,0.00010970891,0.00039929128,0.00019323663,0.007142764],"genre_scores_gemma":[0.9968178,0.0003338219,0.0016321776,0.0001707459,0.000033120305,0.000012774338,0.00011405683,0.000014202395,0.00087126665],"study_design_codex":"case_report","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99979824,0.000026192385,0.000017672679,0.000063647596,0.00005020913,0.000044115914],"domain_scores_gemma":[0.99972945,0.000075195625,0.000048899754,0.000012692251,0.000026735202,0.00010710615],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0001615968,0.0008253736,0.000272395,0.0010409767,0.00048498562,0.00023616983,0.0004117837,0.0012612747,0.0018165014],"category_scores_gemma":[0.0011799257,0.00018832945,0.0002816565,0.00034447748,0.00049252727,0.00036918803,0.00048326043,0.0007810806,0.0006255717],"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":[0.00020082798,0.000047989382,0.062692896,0.000044898985,0.00001523956,0.86888117,0.0003785308,0.00021037602,0.05400028,0.00037349673,0.00067505863,0.012479282],"study_design_scores_gemma":[0.000008602374,0.00027486397,0.04874001,0.000023504408,0.000026540296,0.9357675,0.00014950182,0.00096707937,0.011978301,0.00030703173,0.0017366207,0.000020535661],"about_ca_topic_score_codex":0.0017589729,"about_ca_topic_score_gemma":0.0013740911,"teacher_disagreement_score":0.0018165014,"about_ca_system_score_codex":0.00027201817,"about_ca_system_score_gemma":0.0003161013,"threshold_uncertainty_score":0.0060768127},"labels":[],"label_agreement":null},{"id":"W4392963254","doi":"10.1186/s42269-024-01184-4","title":"Craniofacial anthropometric measurements of the cohort of Egyptian male school children and their utility in detection of abnormalities","year":2024,"lang":"en","type":"article","venue":"Bulletin of the National Research Centre/Bulletin of the National Research Center","topic":"Genetic Syndromes and Imprinting","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":"Polytechnique Montréal","funders":"National Research Centre","keywords":"Craniofacial; Anthropometry; Cohort; Medicine; Pediatrics; Demography; Internal medicine; Psychiatry; Sociology","score_opus":0.055547979690193,"score_gpt":0.34230058108356926,"score_spread":0.28675260139337627,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4392963254","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99950266,0.000055736207,0.000037998678,0.000008397984,0.0000011939488,0.000004288044,0.00017923005,0.000001871083,0.00020863867],"genre_scores_gemma":[0.9993387,0.00007279618,0.0001428117,0.0000060701186,0.000002130422,0.000009991741,0.00023900678,0.0000011914306,0.00018724664],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9997353,0.000043227166,0.000038220813,0.00006541421,0.00007583891,0.000042051117],"domain_scores_gemma":[0.9995403,0.00005815949,0.00020540335,0.00004143656,0.00009821479,0.000056464054],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0003515098,0.00027485768,0.00019067731,0.0010967692,0.00034078702,0.00040466528,0.00023049199,0.00022051299,0.0015196985],"category_scores_gemma":[0.0009809148,0.00018257243,0.00022716181,0.00060606125,0.00026416755,0.0001904175,0.00035908082,0.00025155852,0.00021641752],"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":[0.000037017795,0.000016780126,0.9971643,0.0000059345225,0.00001074346,0.0000988609,0.00012630329,0.000015976551,0.000651952,0.000009181974,0.000034415516,0.0018284864],"study_design_scores_gemma":[4.199957e-7,0.000023185852,0.9995788,0.0000012289457,0.0000030494043,0.00012396775,0.00013766388,0.000015650794,0.000072713396,0.0000015840136,0.000041169907,6.2311665e-7],"about_ca_topic_score_codex":0.007576503,"about_ca_topic_score_gemma":0.009053117,"teacher_disagreement_score":0.007576503,"about_ca_system_score_codex":0.00025698682,"about_ca_system_score_gemma":0.00024115069,"threshold_uncertainty_score":0.015064776},"labels":[],"label_agreement":null},{"id":"W4393313966","doi":"10.1177/23333936241242929","title":"<i>“Unable to Feed My Hungry Child”</i> : Experiences of Mothers Caring for Children With Prader-Willi Syndrome","year":2024,"lang":"en","type":"article","venue":"Global Qualitative Nursing Research","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":5,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":true,"ca_institutions":"University of Victoria; University of Calgary; Mount Royal University","funders":"Mount Royal University","keywords":"Narrative; Harm; Narrative inquiry; Psychological intervention; Psychology; Health care; Nursing; Care work; Social work; Developmental psychology; Work (physics); Medicine; Social psychology","score_opus":0.040380520247156694,"score_gpt":0.41724506398624933,"score_spread":0.3768645437390926,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4393313966","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.98924094,0.0010147877,0.0005698559,0.0045304266,0.00012047759,0.00005643236,0.000076619806,0.000022890696,0.0043675182],"genre_scores_gemma":[0.99375796,0.001240421,0.0007483778,0.0014323198,0.00002661947,0.00009353794,0.00004955843,0.000029928187,0.0026211985],"study_design_codex":"qualitative","study_design_gemma":"qualitative","domain_scores_codex":[0.9969217,0.0018568105,0.00010090154,0.00018427683,0.00028243806,0.0006538027],"domain_scores_gemma":[0.9952732,0.0027404039,0.0006573201,0.0001512488,0.00043515433,0.00074268604],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.004847689,0.0006609546,0.00075711,0.0006212214,0.012109646,0.003925226,0.0019353752,0.0018610947,0.00219937],"category_scores_gemma":[0.009995893,0.0007554196,0.00046458023,0.0006144491,0.009112362,0.0030023027,0.005096014,0.0035455448,0.00031152065],"study_design_candidate":"qualitative","study_design_consensus":"qualitative","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.000019584064,0.000010654315,0.002094919,0.000052971613,0.0000034204093,0.0010494998,0.994105,0.0000107388605,0.0003337208,0.00027990894,0.0006418377,0.0013976947],"study_design_scores_gemma":[0.0000021992378,0.000021901615,0.0011426533,0.000070919086,0.000004657625,0.00048295074,0.9945669,0.000014894539,0.00010749831,0.00007029669,0.0035047082,0.000010373016],"about_ca_topic_score_codex":0.09065737,"about_ca_topic_score_gemma":0.16572525,"teacher_disagreement_score":0.09065737,"about_ca_system_score_codex":0.007960436,"about_ca_system_score_gemma":0.0063933437,"threshold_uncertainty_score":0.18025935},"labels":[],"label_agreement":null},{"id":"W4393979228","doi":"10.1172/jci.insight.169425","title":"Characterization of HMGA2 variants expands the spectrum of Silver-Russell syndrome","year":2024,"lang":"en","type":"article","venue":"JCI Insight","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":9,"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 Manitoba","funders":"Natural Sciences and Engineering Research Council of Canada; Medical Research Council; Children's Hospital Research Institute of Manitoba; National Institute for Health and Care Research; Barts Charity","keywords":"Missense mutation; HMGA2; Phenotype; Biology; Frameshift mutation; Nonsense; Exome sequencing; Genetics; Gene","score_opus":0.008349228860406082,"score_gpt":0.22047653144521603,"score_spread":0.21212730258480994,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4393979228","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9966988,0.00035114115,0.0015740282,0.000039299528,0.0000067822243,0.000022244145,0.00038985204,0.000059153615,0.00085872255],"genre_scores_gemma":[0.9973822,0.0001987587,0.0015660854,0.000036890648,0.0000092754,0.000009110182,0.00042366466,0.000025819825,0.00034808766],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.99980265,0.000022228673,0.000033900687,0.000060539962,0.000058732992,0.000022011516],"domain_scores_gemma":[0.99978465,0.000055845903,0.000050193707,0.000024498715,0.000025942416,0.000058822967],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00019565679,0.00050252635,0.00034378716,0.0008742715,0.00014687583,0.00021725755,0.00018426782,0.00027641896,0.0015976698],"category_scores_gemma":[0.00041390577,0.00014217012,0.00030621182,0.000331692,0.00025864135,0.00012739762,0.00039903977,0.00026935997,0.00032432112],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0005101811,0.00005198237,0.07026174,0.00007281789,0.000109377266,0.021425484,0.0002925399,0.00024932105,0.89681584,0.00026571238,0.0002341279,0.009710989],"study_design_scores_gemma":[0.00013973817,0.00079168426,0.58501405,0.00007264886,0.00035186298,0.21805161,0.0003682982,0.0018960536,0.18493319,0.00082567055,0.007505129,0.00004999005],"about_ca_topic_score_codex":0.0005072443,"about_ca_topic_score_gemma":0.00061021995,"teacher_disagreement_score":0.0015976698,"about_ca_system_score_codex":0.000080626625,"about_ca_system_score_gemma":0.000087266926,"threshold_uncertainty_score":0.0053447485},"labels":[],"label_agreement":null},{"id":"W4394533346","doi":"10.6084/m9.figshare.20064356","title":"Additional file 2 of Gain and loss of TASK3 channel function and its regulation by novel variation cause KCNK9 imprinting syndrome","year":2022,"lang":"en","type":"dataset","venue":"Open MIND","topic":"Genetic Syndromes and Imprinting","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":"BC Children's Hospital","funders":"","keywords":"Imprinting (psychology); Loss function; Variation (astronomy); Function (biology); Biology; Genetics; Phenotype; Gene; Physics","score_opus":0.015247790909407094,"score_gpt":0.24014230705323636,"score_spread":0.22489451614382927,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4394533346","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":[0.00011957775,0.00002563917,0.00003873852,0.000035467292,0.000006815352,0.000009951284,0.99951947,0.000045096567,0.00019928931],"genre_scores_gemma":[0.0025211314,0.00007949788,0.00040096662,0.0001813865,0.000021561458,0.00023523577,0.9952402,0.00008578286,0.0012341234],"study_design_codex":"not_applicable","study_design_gemma":"not_applicable","domain_scores_codex":[0.9993994,0.00008979393,0.00009385891,0.00021806269,0.00009672625,0.000102144484],"domain_scores_gemma":[0.99434644,0.00375468,0.00047682942,0.00051165815,0.00060536526,0.00030501836],"candidate_categories":["insufficient_payload"],"consensus_categories":[],"category_scores_codex":[0.0010006555,0.0012495492,0.0014873764,0.0016229461,0.00073325797,0.0018703777,0.002084117,0.001859039,0.4036107],"category_scores_gemma":[0.012489158,0.0004653011,0.0013138433,0.0030129636,0.00034120187,0.0011039912,0.001081975,0.0014266974,0.06571963],"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":[0.00033874603,0.00006284676,0.005302054,0.0024568455,0.00012733007,0.00011149531,0.000034678626,0.0005216218,0.00016204645,0.000664998,0.9864036,0.0038136397],"study_design_scores_gemma":[0.0065082056,0.0002230518,0.043945882,0.0031319791,0.00057744933,0.0010168267,0.00024581252,0.0018114237,0.0010589398,0.009926427,0.9314195,0.00013459232],"about_ca_topic_score_codex":0.010287626,"about_ca_topic_score_gemma":0.01957638,"teacher_disagreement_score":0.4036107,"about_ca_system_score_codex":0.00097080576,"about_ca_system_score_gemma":0.0018414004,"threshold_uncertainty_score":0.85067695},"labels":[],"label_agreement":null},{"id":"W4394820316","doi":"10.1002/brb3.3437","title":"Expanding deep phenotypic spectrum associated with atypical pathogenic structural variations overlapping 15q11–q13 imprinting region","year":2024,"lang":"en","type":"article","venue":"Brain and Behavior","topic":"Genetic Syndromes and Imprinting","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":"Genome Canada","funders":"","keywords":"Imprinting (psychology); Phenotype; Biology; Genetics; Genomic imprinting; Gene; DNA methylation; Gene expression","score_opus":0.011160155900873575,"score_gpt":0.2493671151816012,"score_spread":0.23820695928072763,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4394820316","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99694425,0.00031476095,0.00057121547,0.00006200275,0.0000052516098,0.00001969597,0.00073451287,0.000029601262,0.0013187346],"genre_scores_gemma":[0.99833775,0.00023136217,0.00047110094,0.00005026534,0.0000059469826,0.000007956613,0.00043060657,0.000012399552,0.00045263403],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9997236,0.000023676273,0.000025925276,0.00011821688,0.00006032736,0.00004822586],"domain_scores_gemma":[0.99971336,0.000069005044,0.00009356625,0.000024542544,0.000036404985,0.00006315029],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00020254539,0.00059003825,0.00033724384,0.0013501921,0.0004372285,0.0004358158,0.0003311656,0.00037718547,0.0057243626],"category_scores_gemma":[0.00087606645,0.00016701852,0.00027629483,0.0009057239,0.00039730433,0.00021354663,0.0007303763,0.00028449815,0.000473076],"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":[0.0005942448,0.000047286525,0.8751289,0.00009865024,0.00012884001,0.04898835,0.00064515823,0.00035844382,0.054357473,0.00046008924,0.0008344833,0.018358156],"study_design_scores_gemma":[0.000027323193,0.00014482558,0.8711944,0.0000654664,0.0001456697,0.11946151,0.00060630747,0.0005070734,0.0047306153,0.0006494765,0.0024456838,0.000021647431],"about_ca_topic_score_codex":0.00235948,"about_ca_topic_score_gemma":0.0027413408,"teacher_disagreement_score":0.0057243626,"about_ca_system_score_codex":0.00019533618,"about_ca_system_score_gemma":0.00020147677,"threshold_uncertainty_score":0.0191499},"labels":[],"label_agreement":null},{"id":"W4394903714","doi":"10.1016/j.lingua.2024.103724","title":"The linguistic and metalinguistic abilities of monolingual and bilingual speakers with Prader–Willi syndrome","year":2024,"lang":"en","type":"article","venue":"Lingua","topic":"Genetic Syndromes and Imprinting","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":"Wilfrid Laurier University; University of Ottawa","funders":"","keywords":"Grammaticality; Neuroscience of multilingualism; Psychology; Linguistics; Metalinguistic awareness; Catalan; Semantics (computer science); Multilingualism; Grammar; Computer science","score_opus":0.006109767730625988,"score_gpt":0.2346713497487275,"score_spread":0.2285615820181015,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4394903714","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9997321,0.000015242164,0.00001694308,0.0000038447365,7.3541673e-7,0.0000011133155,0.000013793976,8.8150836e-7,0.00021531119],"genre_scores_gemma":[0.9995104,0.000024144934,0.00007083277,0.000007304289,0.0000014635294,0.0000034704387,0.000034647594,0.0000018405154,0.00034590688],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.999801,0.000035939287,0.00002444264,0.000053759577,0.000041058007,0.000043963573],"domain_scores_gemma":[0.99959844,0.0001305511,0.00008963802,0.000029319744,0.00006593439,0.0000862038],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0002746154,0.00031963937,0.00019455716,0.0007533801,0.00037247912,0.0004143493,0.00012598636,0.00020186981,0.0018544252],"category_scores_gemma":[0.00170636,0.00012844175,0.00011454781,0.000174751,0.0004844273,0.0002950218,0.00061573327,0.0002244812,0.00035051847],"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":[0.0011984442,0.00039965266,0.8677976,0.000086693304,0.000086902146,0.004688867,0.01580764,0.00018654492,0.08416809,0.00026568052,0.00026049235,0.025053384],"study_design_scores_gemma":[0.000013641174,0.00031667578,0.98917526,0.000007786781,0.00002366382,0.0039457385,0.0035259768,0.00019919555,0.0023174654,0.0001719431,0.00028896038,0.0000136310555],"about_ca_topic_score_codex":0.0040215612,"about_ca_topic_score_gemma":0.0051351073,"teacher_disagreement_score":0.0040215612,"about_ca_system_score_codex":0.00016196471,"about_ca_system_score_gemma":0.00022461844,"threshold_uncertainty_score":0.007996321},"labels":[],"label_agreement":null},{"id":"W4396541254","doi":"10.1016/j.parkreldis.2024.106782","title":"Intronic GAA-FGF14 Expansion in an italian patient presenting with early-onset cerebellar ataxia","year":2024,"lang":"en","type":"article","venue":"Parkinsonism & Related Disorders","topic":"Genetic Syndromes and Imprinting","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 de réadaptation Lethbridge-Layton-Mackay; McGill University; Montreal Neurological Institute and Hospital","funders":"","keywords":"Ataxia; Cerebellar ataxia; Medicine; Trinucleotide repeat expansion; Neuroscience; Psychology; Pediatrics; Genetics; Biology; Allele; Gene","score_opus":0.004506469812084299,"score_gpt":0.21869580084253476,"score_spread":0.21418933103045046,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4396541254","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9941402,0.00055717136,0.0005981973,0.00063711934,0.000069343405,0.00003845544,0.00019925139,0.000043856046,0.0037163661],"genre_scores_gemma":[0.99784327,0.00020815169,0.000455203,0.000247483,0.00013348732,0.000009053414,0.00010950647,0.000017175234,0.0009767552],"study_design_codex":"case_report","study_design_gemma":"case_report","domain_scores_codex":[0.99976677,0.000035541798,0.00002931909,0.00007088447,0.000034947352,0.00006263114],"domain_scores_gemma":[0.999283,0.00030077153,0.00017483685,0.00003455814,0.000045193825,0.00016165002],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00020004874,0.0018853159,0.000504833,0.0011243825,0.0010135088,0.0005079185,0.00079922745,0.0021261768,0.0020943906],"category_scores_gemma":[0.0015538231,0.0004176857,0.0007044822,0.0008352817,0.0009581192,0.00027345898,0.00046141713,0.00062741403,0.00060268864],"study_design_candidate":"case_report","study_design_consensus":"case_report","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00011675628,0.00004464797,0.023670942,0.00002210608,0.000017403629,0.96908176,0.0002551778,0.00014753285,0.0047768536,0.00011824123,0.00026909538,0.0014794476],"study_design_scores_gemma":[0.000037752576,0.00017649625,0.07530321,0.000030068994,0.00012223578,0.92030364,0.00021354784,0.00066424767,0.0017677994,0.00014686758,0.0012076712,0.000026535847],"about_ca_topic_score_codex":0.0052468074,"about_ca_topic_score_gemma":0.003908356,"teacher_disagreement_score":0.0052468074,"about_ca_system_score_codex":0.0005923008,"about_ca_system_score_gemma":0.0005956628,"threshold_uncertainty_score":0.010432541},"labels":[],"label_agreement":null},{"id":"W4396577216","doi":"10.1101/2024.05.01.591988","title":"Atlas of imprinted and allele-specific DNA methylation in the human body","year":2024,"lang":"en","type":"preprint","venue":"bioRxiv (Cold Spring Harbor Laboratory)","topic":"Genetic Syndromes and Imprinting","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":"Institute of Cancer Research","funders":"","keywords":"Atlas (anatomy); DNA methylation; Allele; Genomic imprinting; Genetics; Methylation; Biology; DNA; Gene; Anatomy; Gene expression","score_opus":0.012893020779266278,"score_gpt":0.23550915114002885,"score_spread":0.22261613036076258,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4396577216","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.5534552,0.016616432,0.11768651,0.0006139369,0.00015808141,0.00020679063,0.2778863,0.009619809,0.023756886],"genre_scores_gemma":[0.7618979,0.0055394205,0.073477075,0.0003015227,0.000059993516,0.00035959636,0.14480564,0.0007335171,0.012825259],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.99986994,0.000019773353,0.000007854278,0.000048154416,0.00003773766,0.000016422448],"domain_scores_gemma":[0.9998802,0.000017753797,0.000025087009,0.000032337786,0.000019458197,0.000025296216],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00018406114,0.0002441718,0.00035359382,0.0011442363,0.0002159692,0.00034011644,0.0003159609,0.00025427953,0.0044181957],"category_scores_gemma":[0.00020020713,0.00023505447,0.0002669519,0.0013378366,0.00014850874,0.00016625963,0.00056377955,0.00034871843,0.001315998],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00091952644,0.000030942418,0.04255358,0.0016352305,0.00047685043,0.0005942489,0.00029404942,0.004691584,0.8133869,0.003356749,0.0266836,0.105376795],"study_design_scores_gemma":[0.00009576418,0.00023215624,0.5207319,0.00014174113,0.00056536414,0.0040777284,0.00016701219,0.010899751,0.20988022,0.0058970586,0.24723001,0.0000812121],"about_ca_topic_score_codex":0.001897899,"about_ca_topic_score_gemma":0.0032957054,"teacher_disagreement_score":0.0044181957,"about_ca_system_score_codex":0.00029484637,"about_ca_system_score_gemma":0.00043243007,"threshold_uncertainty_score":0.014780343},"labels":[],"label_agreement":null},{"id":"W4396900582","doi":"10.1002/ajmg.a.63625","title":"Adults with paternal <scp>UPD14</scp> causing <scp>Kagami–Ogata</scp> syndrome: Case report and review of the literature","year":2024,"lang":"en","type":"review","venue":"American Journal of Medical Genetics Part A","topic":"Genetic Syndromes and Imprinting","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":"Queen's University; Alberta Children's Hospital; University of Calgary","funders":"","keywords":"Neurocognitive; Uniparental disomy; Natural history; Medicine; Pediatrics; Genetics; Biology; Chromosome; Internal medicine; Psychiatry; Gene; Karyotype","score_opus":0.011795043137920696,"score_gpt":0.2921715514607239,"score_spread":0.2803765083228032,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4396900582","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":[0.000754894,0.99737775,0.0001860007,0.0002788989,0.00018766505,0.0000046379596,0.000035929294,0.000014084922,0.0011601654],"genre_scores_gemma":[0.0028162736,0.995977,0.0002606834,0.00024206818,0.00024807395,0.000004198785,0.00006267837,0.0000029430278,0.0003861652],"study_design_codex":"design_other","study_design_gemma":"case_report","domain_scores_codex":[0.99985325,0.00001635241,0.00004233862,0.00003415814,0.0000390562,0.00001483102],"domain_scores_gemma":[0.9997279,0.00014211964,0.000056140325,0.000008061867,0.00003814123,0.000027676844],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00027158487,0.0007802916,0.001141744,0.00361855,0.0002918438,0.00068189105,0.0007811718,0.00084538676,0.0026565038],"category_scores_gemma":[0.0007317816,0.00022254935,0.0004089284,0.0027295218,0.00042116016,0.0011573354,0.0005072888,0.0008683363,0.0013395961],"study_design_candidate":"case_report","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00007281801,0.000060457376,0.002113861,0.01882383,0.00018497556,0.019358544,0.00018006549,0.0003628604,0.0020843123,0.0012475359,0.031015938,0.9244949],"study_design_scores_gemma":[0.000024865907,0.000099113095,0.0071941908,0.012057215,0.00056428445,0.2716544,0.0004011807,0.00015646989,0.0010258245,0.0018756137,0.7048779,0.000069001384],"about_ca_topic_score_codex":0.0008985123,"about_ca_topic_score_gemma":0.001714653,"teacher_disagreement_score":0.00361855,"about_ca_system_score_codex":0.0003002151,"about_ca_system_score_gemma":0.0007046876,"threshold_uncertainty_score":0.008886814},"labels":[],"label_agreement":null},{"id":"W4397048300","doi":"10.1681/asn.20233411s1809b","title":"A Case of Primary Pseudohypoparathyroidism Presenting with Normal Serum Phosphorus","year":2023,"lang":"en","type":"article","venue":"Journal of the American Society of Nephrology","topic":"Genetic Syndromes and Imprinting","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":"Wilfrid Laurier University","funders":"","keywords":"Pseudohypoparathyroidism; Phosphorus; Endocrinology; Internal medicine; Medicine; Primary (astronomy); Parathyroid hormone; Chemistry; Calcium","score_opus":0.011535097335196963,"score_gpt":0.24277431809430894,"score_spread":0.23123922075911196,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4397048300","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.94855577,0.01114189,0.005246521,0.006410397,0.0009837082,0.00033191335,0.0007767277,0.00045038108,0.026102781],"genre_scores_gemma":[0.9940943,0.0011761963,0.0013330738,0.0008461678,0.0009372818,0.00003690893,0.00012793425,0.00003254199,0.0014154888],"study_design_codex":"case_report","study_design_gemma":"case_report","domain_scores_codex":[0.9988986,0.000092002476,0.000103154096,0.0003120452,0.00018627207,0.0004079602],"domain_scores_gemma":[0.9979159,0.0005260254,0.0004993701,0.00020080015,0.00013484631,0.0007229543],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00031086704,0.0020464582,0.0014387976,0.0032307687,0.002665713,0.0021570865,0.0017386664,0.006137385,0.004576264],"category_scores_gemma":[0.0034023346,0.0014605306,0.0013742292,0.0024149467,0.0019131008,0.002290891,0.002491258,0.0035613598,0.001298016],"study_design_candidate":"case_report","study_design_consensus":"case_report","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.000013231747,0.000010572686,0.001392033,0.000015708638,0.000002734565,0.9977192,0.000050106828,0.00002157614,0.00025026168,0.00006972977,0.00010843283,0.0003464104],"study_design_scores_gemma":[0.0000055378337,0.000012638179,0.0006369177,0.0000040043174,0.0000032022933,0.99891484,0.00003111485,0.000056709792,0.00008522652,0.000060789225,0.00018650688,0.0000025510342],"about_ca_topic_score_codex":0.002792197,"about_ca_topic_score_gemma":0.0024911002,"teacher_disagreement_score":0.006137385,"about_ca_system_score_codex":0.0016037448,"about_ca_system_score_gemma":0.0012156236,"threshold_uncertainty_score":0.015309155},"labels":[],"label_agreement":null},{"id":"W4399868159","doi":"10.3389/fendo.2024.1403470","title":"Puberty in girls with Prader-Willi syndrome: cohort evaluation and clinical recommendations in a Latin American tertiary center","year":2024,"lang":"en","type":"article","venue":"Frontiers in Endocrinology","topic":"Genetic Syndromes and Imprinting","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":"Children's Hospital of Western Ontario; London Health Sciences Centre; Western University","funders":"","keywords":"Adrenarche; Medicine; Menarche; Precocious puberty; Breast development; Bone age; Body mass index; Pediatrics; Cohort; Pubic hair; Gynecology; Endocrinology; Internal medicine; Hormone","score_opus":0.01361965296480214,"score_gpt":0.30474418857863667,"score_spread":0.2911245356138345,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4399868159","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9984964,0.00019740325,0.00008139158,0.00013063234,0.0000046448495,0.00007244213,0.0005528735,0.0000063709604,0.00045779254],"genre_scores_gemma":[0.99805707,0.000379407,0.0003071553,0.00006788821,0.000010538711,0.00010268222,0.00094239257,0.000004741547,0.00012817065],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99953175,0.00012876511,0.00006124236,0.00011963556,0.00006500708,0.000093557275],"domain_scores_gemma":[0.99889094,0.00013028426,0.0004580031,0.00007746055,0.00019025052,0.00025310807],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0011493991,0.00024153154,0.00038315478,0.0015915319,0.0009183966,0.0007367851,0.0005325546,0.0003440967,0.0014995235],"category_scores_gemma":[0.0022793086,0.00023128252,0.0004195725,0.0014453145,0.00026233186,0.0005550464,0.00079051737,0.00028579216,0.0002377885],"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":[0.000019976856,0.00003111208,0.99892116,0.0000048207253,0.0000042520205,0.00010085863,0.000092354865,0.0000046092955,0.00004910743,0.000008569843,0.00006205714,0.0007011393],"study_design_scores_gemma":[0.000015482852,0.00011762809,0.9971418,0.000029894169,0.000015950125,0.00061479467,0.001533054,0.00011684858,0.00004494503,0.000018370778,0.00034732174,0.0000038336966],"about_ca_topic_score_codex":0.015661959,"about_ca_topic_score_gemma":0.01814432,"teacher_disagreement_score":0.015661959,"about_ca_system_score_codex":0.000634159,"about_ca_system_score_gemma":0.0013384918,"threshold_uncertainty_score":0.03114158},"labels":[],"label_agreement":null},{"id":"W4400680892","doi":"10.1075/bpa.18.11gar","title":"The narrative abilities of Spanish monolinguals and Spanish–Catalan bilinguals with Prader–Willi syndrome","year":2024,"lang":"en","type":"book-chapter","venue":"Bilingual processing and acquisition","topic":"Genetic Syndromes and Imprinting","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":"University of Ottawa","funders":"","keywords":"Catalan; Narrative; Psychology; Linguistics; Philosophy","score_opus":0.008256167356345505,"score_gpt":0.23601341544831253,"score_spread":0.227757248091967,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4400680892","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9984309,0.0001241688,0.000024312869,0.00001445335,0.0000021504775,0.0000034571722,0.00003800901,0.0000018089539,0.001360617],"genre_scores_gemma":[0.99842477,0.000112162685,0.000068280475,0.000018899333,0.0000023536006,0.000007896783,0.00009775188,0.0000027346412,0.0012651808],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9997985,0.00004501418,0.000020683423,0.0000431045,0.00005235499,0.000040384482],"domain_scores_gemma":[0.99930227,0.00021660583,0.0001443919,0.000036725927,0.00016432272,0.00013570755],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00042106182,0.00032011876,0.00025225308,0.0008712125,0.00046354427,0.00078997883,0.00018761164,0.00025893818,0.0032199335],"category_scores_gemma":[0.0015391888,0.00012886549,0.00010926846,0.00025556723,0.0005263115,0.00032598857,0.00055029185,0.000223259,0.00049348385],"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":[0.0010466557,0.00072396256,0.81291884,0.00016829888,0.000059389273,0.0074675735,0.08525606,0.00016440745,0.03524226,0.00041686802,0.0013760864,0.055159513],"study_design_scores_gemma":[0.000038318347,0.00035678703,0.9552416,0.000035805773,0.000023008632,0.007094688,0.033169128,0.00022829545,0.0014831722,0.0002791474,0.0020220252,0.000027992517],"about_ca_topic_score_codex":0.010291152,"about_ca_topic_score_gemma":0.011142511,"teacher_disagreement_score":0.010291152,"about_ca_system_score_codex":0.0003484423,"about_ca_system_score_gemma":0.0003259435,"threshold_uncertainty_score":0.020462513},"labels":[],"label_agreement":null},{"id":"W4401041830","doi":"","title":"D’une myopathie centronucléaire du Labrador aux rôles des acides gras à très longue chaîne chez les mammifères : Étude des gènes Hacd","year":2013,"lang":"fr","type":"dissertation","venue":"HAL (Le Centre pour la Communication Scientifique Directe)","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":0,"is_retracted":false,"has_abstract":false,"route_ca_aff":false,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":true,"ca_institutions":"","funders":"","keywords":"Humanities; Art","score_opus":0.010689998265768257,"score_gpt":0.2175778906622948,"score_spread":0.20688789239652655,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4401041830","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":[0.99048424,0.003408493,0.0031269097,0.00060437556,0.000107566484,0.000040114814,0.00010886227,0.000037786835,0.002081689],"genre_scores_gemma":[0.99334586,0.0012755529,0.00084290846,0.00029058105,0.00006201135,0.000024920973,0.00007409793,0.000014901726,0.004069141],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9997565,0.000030202133,0.000015575606,0.000100035526,0.000042502365,0.00005510069],"domain_scores_gemma":[0.9995372,0.0002580564,0.000065115404,0.000021546648,0.00006314422,0.000055025386],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0003193159,0.0006939744,0.0003586843,0.00075961265,0.00093142653,0.0003263474,0.0003190889,0.0011565886,0.0028810508],"category_scores_gemma":[0.0007280348,0.00039565153,0.0006294736,0.00026108426,0.0014036107,0.00041168046,0.00030084772,0.0008776694,0.00045768617],"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":[0.003504658,0.00027891315,0.05194877,0.0004781406,0.00027940437,0.20451,0.0031798433,0.00065060274,0.7076068,0.0010964116,0.0008149138,0.0256516],"study_design_scores_gemma":[0.00033040994,0.002445736,0.44162142,0.00012469725,0.0005615255,0.36724538,0.0016766357,0.0012169328,0.1694267,0.00045146444,0.01481338,0.0000857169],"about_ca_topic_score_codex":0.014162889,"about_ca_topic_score_gemma":0.011246485,"teacher_disagreement_score":0.014162889,"about_ca_system_score_codex":0.00057174446,"about_ca_system_score_gemma":0.00031447093,"threshold_uncertainty_score":0.02816093},"labels":[],"label_agreement":null},{"id":"W4401745747","doi":"10.36557/pbpc.v3i2.148","title":"SÍNDROME DE PERLMAN: CORRELAÇÕES ENTRE MUTAÇÃO GENÉTICA, MANIFESTAÇÕES CLÍNICAS E PROGNÓSTICO DE SOBREVIVÊNCIA: UMA REVISÃO SISTEMÁTICA.","year":2024,"lang":"pt","type":"article","venue":"Periódicos Brasil Pesquisa Científica","topic":"Genetic Syndromes and Imprinting","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":"Centre Intégré de Santé et de Services Sociaux des Laurentides","funders":"","keywords":"Medicine","score_opus":0.015175228881172101,"score_gpt":0.27333768476774833,"score_spread":0.2581624558865762,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4401745747","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":[0.033504177,0.94636995,0.0051920675,0.007031254,0.0008176919,0.00019320822,0.0015203862,0.00008939846,0.0052818763],"genre_scores_gemma":[0.24348953,0.73328453,0.012930045,0.0027535246,0.0018315613,0.0003787615,0.0022924142,0.000045639783,0.0029939483],"study_design_codex":"design_other","study_design_gemma":"systematic_review","domain_scores_codex":[0.9956707,0.0018764291,0.0007241057,0.0006564028,0.00092305907,0.00014927167],"domain_scores_gemma":[0.98349726,0.009155436,0.0040516923,0.0005838344,0.002427472,0.00028432932],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.008396862,0.0011070721,0.002294914,0.0062020887,0.0007876502,0.0035055932,0.001500302,0.0012432631,0.0051711765],"category_scores_gemma":[0.017191624,0.00055553234,0.001990634,0.0074960077,0.0015636941,0.0033272535,0.0015125106,0.0020542126,0.00068988267],"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":[0.00083044625,0.00026667528,0.1992352,0.023164494,0.0020697964,0.00095607527,0.0017607436,0.00077904615,0.0020241851,0.009837736,0.011183693,0.74789196],"study_design_scores_gemma":[0.00023308187,0.0029476525,0.43824986,0.07941767,0.010977694,0.020163305,0.0064411326,0.0049058907,0.0062164688,0.03266667,0.3972048,0.00057579356],"about_ca_topic_score_codex":0.009343616,"about_ca_topic_score_gemma":0.012730262,"teacher_disagreement_score":0.009343616,"about_ca_system_score_codex":0.0024917782,"about_ca_system_score_gemma":0.004331837,"threshold_uncertainty_score":0.044407368},"labels":[],"label_agreement":null},{"id":"W4402900588","doi":"10.1002/ajmg.a.63864","title":"Diagnosis of <i>TET3</i>‐Related Beck–Fahrner Syndrome in an Individual With Chorioretinal and Iris Colobomata Using a <scp>DNA</scp> Methylation Signature","year":2024,"lang":"en","type":"article","venue":"American Journal of Medical Genetics Part A","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","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":"Hospital for Sick Children; McMaster Children's Hospital; Western University; London Health Sciences Centre; McMaster University","funders":"Government of Canada; Ontario Genomics; Genome Canada","keywords":"Epigenetics; Genetics; DNA methylation; Phenotype; Biology; Mendelian inheritance; Gene","score_opus":0.012154073577251978,"score_gpt":0.27700099732080485,"score_spread":0.2648469237435529,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4402900588","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99131984,0.00027717848,0.0021208855,0.00059685844,0.000035826946,0.00007125338,0.00012377158,0.00009023838,0.005364203],"genre_scores_gemma":[0.9978823,0.0001381406,0.0013196494,0.00010677377,0.000033351946,0.000007850815,0.00003769918,0.000008724961,0.0004655812],"study_design_codex":"case_report","study_design_gemma":"case_report","domain_scores_codex":[0.99975497,0.000032343327,0.000022056149,0.00008018085,0.000048083442,0.0000624707],"domain_scores_gemma":[0.9997578,0.00006359017,0.000050863593,0.000010876381,0.000014343234,0.0001025206],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00018260046,0.0010265562,0.0003464707,0.0010122552,0.00082373654,0.00044867385,0.00033801488,0.0011580724,0.0017174435],"category_scores_gemma":[0.0008009108,0.0003366632,0.0002862989,0.000339817,0.00071583356,0.0004258113,0.00058581657,0.0008267412,0.000295355],"study_design_candidate":"case_report","study_design_consensus":"case_report","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00011698962,0.00007063539,0.088827506,0.00003805279,0.000022267148,0.8688204,0.00083295023,0.00028440286,0.032010935,0.0006810327,0.00061286247,0.0076820096],"study_design_scores_gemma":[0.0000093029375,0.00021219013,0.057260506,0.00002494208,0.000039983726,0.9340727,0.00034158528,0.0010061346,0.0056745233,0.00041053668,0.000916848,0.000030728737],"about_ca_topic_score_codex":0.0018766436,"about_ca_topic_score_gemma":0.0021672517,"teacher_disagreement_score":0.0018766436,"about_ca_system_score_codex":0.0002607912,"about_ca_system_score_gemma":0.00033998908,"threshold_uncertainty_score":0.005745411},"labels":[],"label_agreement":null},{"id":"W4402953928","doi":"","title":"[Angelman syndrome: current approach and the future of therapies].","year":2024,"lang":"en","type":"review","venue":"PubMed","topic":"Genetic Syndromes and Imprinting","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":"Children's Hospital of Eastern Ontario","funders":"","keywords":"Angelman syndrome; Current (fluid); Psychology; Computer science; Medicine; Biology; Genetics; Engineering; Electrical engineering","score_opus":0.024940484383216083,"score_gpt":0.2648798148217039,"score_spread":0.23993933043848784,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4402953928","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":[0.000037394053,0.99719775,0.000084700085,0.00049662864,0.0006790271,0.0000039303477,0.00002445113,0.000011105265,0.0014650755],"genre_scores_gemma":[0.00050290226,0.9964012,0.00024025919,0.00067685964,0.00049477245,0.000006904998,0.00006952597,0.0000031067632,0.0016043866],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.99985445,0.000026034344,0.00002594764,0.000020646701,0.000057036134,0.000015803282],"domain_scores_gemma":[0.9997588,0.00009345599,0.000039566396,0.000008522466,0.00006810613,0.000031632415],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00044132824,0.00091139285,0.0010052382,0.0018242281,0.00025309628,0.0009146277,0.0009050295,0.001147465,0.0072768047],"category_scores_gemma":[0.0007917326,0.00017237011,0.00044753362,0.001870716,0.00039100696,0.0013467696,0.0007509302,0.0018335487,0.0045339596],"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":[0.000051519768,0.000024099161,0.00008532828,0.012610415,0.00006518139,0.00027490064,0.000039065802,0.00018416677,0.00059219147,0.0039827703,0.1294378,0.8526526],"study_design_scores_gemma":[0.000015522157,0.00003301747,0.00036086727,0.0044108126,0.000052788393,0.0017346747,0.00003717019,0.000042818385,0.00008656888,0.0019024014,0.9913121,0.000011110379],"about_ca_topic_score_codex":0.001346027,"about_ca_topic_score_gemma":0.0030783287,"teacher_disagreement_score":0.0072768047,"about_ca_system_score_codex":0.0006435089,"about_ca_system_score_gemma":0.001099031,"threshold_uncertainty_score":0.024343312},"labels":[],"label_agreement":null},{"id":"W4403025409","doi":"10.1101/2024.09.30.615881","title":"Quorum sensing and DNA methylation play active roles in clinical <i>Burkholderia</i> phase variation","year":2024,"lang":"en","type":"preprint","venue":"bioRxiv (Cold Spring Harbor Laboratory)","topic":"Genetic Syndromes and Imprinting","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":"Institut National de la Recherche Scientifique","funders":"","keywords":"Quorum sensing; Phase variation; DNA methylation; Variation (astronomy); DNA; Burkholderia; Methylation; Phase (matter); Biofilm; Biology; Computational biology; Genetics; Chemistry; Bacteria; Physics; Gene; Phenotype","score_opus":0.014557304331403976,"score_gpt":0.2720955192083499,"score_spread":0.25753821487694595,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4403025409","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9974821,0.0005110856,0.0012756552,0.00006722936,0.0000052263067,0.000012812996,0.00017088413,0.000030506953,0.0004444704],"genre_scores_gemma":[0.9989723,0.000082812876,0.00057388115,0.000021958593,0.0000030359306,0.000005040564,0.00013210348,0.0000038197454,0.0002051684],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9998814,0.000018524857,0.000011474669,0.00002806664,0.00003005101,0.000030511146],"domain_scores_gemma":[0.9997954,0.000031802814,0.00009725732,0.00001605564,0.000023048486,0.0000365033],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00012768732,0.00016691185,0.00017062092,0.00016184506,0.000090750975,0.000238828,0.0001313885,0.00024962134,0.001098729],"category_scores_gemma":[0.00022861671,0.000097212505,0.00015027035,0.00009824207,0.00019193739,0.00013427333,0.00015725472,0.00022600105,0.00019476355],"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":[0.000100331905,0.0000122653855,0.0028599391,0.00001744435,0.000002417064,0.000034147542,0.000012791403,0.000024028133,0.9957801,0.00004310701,0.00001023891,0.0011031958],"study_design_scores_gemma":[0.00002349036,0.0005167397,0.1427919,0.000015061583,0.000032660755,0.0010680687,0.00011107882,0.0012230218,0.8519245,0.00027123874,0.002008279,0.000013956015],"about_ca_topic_score_codex":0.00068477314,"about_ca_topic_score_gemma":0.0005207009,"teacher_disagreement_score":0.001098729,"about_ca_system_score_codex":0.00015326325,"about_ca_system_score_gemma":0.00010862934,"threshold_uncertainty_score":0.00367558},"labels":[],"label_agreement":null},{"id":"W4403053527","doi":"10.1101/gr.279273.124","title":"High-coverage nanopore sequencing of samples from the 1000 Genomes Project to build a comprehensive catalog of human genetic variation","year":2024,"lang":"en","type":"article","venue":"Genome Research","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":77,"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 Bulletin of Medical History","funders":"National Institute of Allergy and Infectious Diseases; National Institute of Neurological Disorders and Stroke; National Institute of General Medical Sciences; National Human Genome Research Institute; National Institute on Drug Abuse; National Institute on Aging; Fonds Wetenschappelijk Onderzoek; National Institute of Standards and Technology; Lustgarten Foundation; National Cancer Institute; National Institutes of Health; National Science Foundation","keywords":"Biology; Indel; 1000 Genomes Project; Structural variation; Genome; Computational biology; Genetics; Concordance; Human genome; Whole genome sequencing; Personal genomics; DNA sequencing; Nanopore sequencing; Copy-number variation; Single-nucleotide polymorphism; Gene; Genotype","score_opus":0.06116980272795516,"score_gpt":0.3402952870025182,"score_spread":0.2791254842745631,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4403053527","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.93701595,0.0012904226,0.036269765,0.00028904094,0.00003794525,0.00017355337,0.021395452,0.0004324234,0.0030955127],"genre_scores_gemma":[0.88127255,0.0008166757,0.06204537,0.0006295056,0.000037629397,0.00041472373,0.051628765,0.00030856882,0.0028461565],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99945575,0.00008805616,0.000044947887,0.00018664738,0.00017471523,0.000049918406],"domain_scores_gemma":[0.9994172,0.00018363167,0.00007184307,0.00010923629,0.00015252491,0.0000655735],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00064112665,0.00039700905,0.00037510606,0.0011634434,0.00047056438,0.000633669,0.00027229555,0.00043893533,0.0016722598],"category_scores_gemma":[0.0018051622,0.00016797966,0.00042696585,0.0012823518,0.00023550131,0.00020578636,0.0006112084,0.000530664,0.00053543184],"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":[0.0006723689,0.00015985339,0.19127196,0.00039920476,0.00066332245,0.0005203698,0.0014382184,0.005162739,0.7298048,0.0012878109,0.005397458,0.06322195],"study_design_scores_gemma":[0.000055096465,0.00040098844,0.8182838,0.000112294365,0.00032704134,0.0016049623,0.00058828277,0.016031174,0.115925424,0.002618319,0.043994926,0.000057649646],"about_ca_topic_score_codex":0.0051499004,"about_ca_topic_score_gemma":0.01006136,"teacher_disagreement_score":0.0051499004,"about_ca_system_score_codex":0.00032599914,"about_ca_system_score_gemma":0.0003116903,"threshold_uncertainty_score":0.01023984},"labels":[],"label_agreement":null},{"id":"W4403463613","doi":"10.1210/clinem/dgae730","title":"Distinguishing Genetic Alterations Versus (Epi)Mutations in Silver–Russell Syndrome and Focus on the <i>IGF1R</i> Gene","year":2024,"lang":"en","type":"article","venue":"The Journal of Clinical Endocrinology & Metabolism","topic":"Genetic Syndromes and Imprinting","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 Hospital Foundation","funders":"Ministero della Salute","keywords":"Macrocephaly; Genetics; Genetic heterogeneity; Context (archaeology); Genetic testing; Biology; Genotype; Allele; Medicine; Gene; Phenotype","score_opus":0.03834019508968787,"score_gpt":0.3381296966635877,"score_spread":0.29978950157389983,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4403463613","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9990989,0.00021609054,0.00019066161,0.000012749932,0.0000031725983,0.000006906501,0.000074827105,0.0000049348787,0.00039170348],"genre_scores_gemma":[0.9993451,0.00010808401,0.00030027606,0.000017171124,0.0000062944487,0.000005013904,0.0001449992,0.0000025522402,0.00007037603],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9997179,0.00004511421,0.000060955932,0.00008722928,0.000048154212,0.000040667797],"domain_scores_gemma":[0.99923754,0.00032008544,0.00022959795,0.000045681885,0.0000692405,0.00009796636],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0004351016,0.00028346526,0.00022740125,0.0013399924,0.00021451456,0.00035271002,0.00023203726,0.00035978825,0.001505064],"category_scores_gemma":[0.0016003037,0.00010588416,0.0001658516,0.0005050806,0.0003299268,0.00028049375,0.00039297368,0.00015292485,0.00031536864],"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":[0.00030774545,0.000019426583,0.98177123,0.0000310929,0.000024598477,0.0033098676,0.00015430321,0.00006907971,0.008289687,0.000045573415,0.00008776249,0.005889601],"study_design_scores_gemma":[0.000018005283,0.00022047044,0.9766203,0.000018439247,0.00006409444,0.01931598,0.0003236403,0.00039933043,0.0023538533,0.00013931483,0.0005194535,0.0000070785263],"about_ca_topic_score_codex":0.0005991303,"about_ca_topic_score_gemma":0.00095155736,"teacher_disagreement_score":0.001505064,"about_ca_system_score_codex":0.00009078274,"about_ca_system_score_gemma":0.00016332728,"threshold_uncertainty_score":0.005034983},"labels":[],"label_agreement":null},{"id":"W4403513920","doi":"10.1093/omcr/omae114","title":"Rhythmic high-amplitude delta with superimposed spikes (RHADS): a treatment dilemma","year":2024,"lang":"en","type":"article","venue":"Oxford Medical Case Reports","topic":"Genetic Syndromes and Imprinting","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":"BC Children's Hospital","funders":"","keywords":"Pathognomonic; Electroencephalography; Rhythm; Medicine; Subclinical infection; Ictal; Neuroscience; Delta Rhythm; Audiology; Psychology; Psychiatry; Internal medicine; Alpha rhythm","score_opus":0.009904330234463906,"score_gpt":0.25748594776313666,"score_spread":0.24758161752867275,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4403513920","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":[0.115240104,0.11489821,0.024749294,0.70999175,0.005791142,0.00019555508,0.00023604513,0.0005053145,0.02839257],"genre_scores_gemma":[0.76968974,0.06767737,0.02705395,0.10442788,0.024067832,0.00029958884,0.0002986053,0.00020159087,0.00628339],"study_design_codex":"case_report","study_design_gemma":"case_report","domain_scores_codex":[0.99936765,0.00016695047,0.00013373984,0.00009459601,0.00012784226,0.0001092266],"domain_scores_gemma":[0.9978477,0.0009832949,0.00026880417,0.00010858008,0.00020718554,0.0005844039],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0014255194,0.0006985322,0.0010729071,0.00086077926,0.0014398113,0.0010860271,0.0011294537,0.004904598,0.001765394],"category_scores_gemma":[0.005592478,0.00025758884,0.00040638517,0.0005290809,0.0019433803,0.0022766762,0.0014772387,0.00528583,0.0010800106],"study_design_candidate":"case_report","study_design_consensus":"case_report","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00029637676,0.00019638539,0.014426509,0.00088615436,0.000084210384,0.6368859,0.001043194,0.0021324693,0.0031904613,0.017137565,0.062669784,0.261051],"study_design_scores_gemma":[0.00011222234,0.0002902518,0.0050446196,0.0012685038,0.000063445426,0.89816856,0.0026219406,0.0024070526,0.0011485618,0.038243786,0.05054193,0.00008899855],"about_ca_topic_score_codex":0.0005662749,"about_ca_topic_score_gemma":0.0010492976,"teacher_disagreement_score":0.004904598,"about_ca_system_score_codex":0.00094435486,"about_ca_system_score_gemma":0.0011087117,"threshold_uncertainty_score":0.0075389743},"labels":[],"label_agreement":null},{"id":"W4404090810","doi":"10.1183/13993003.congress-2024.pa1356","title":"Oxygenation and ventilation parameters in children with Prader-Willi syndrome without or with growth hormone treatment.","year":2024,"lang":"en","type":"article","venue":"","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":0,"is_retracted":false,"has_abstract":true,"route_ca_aff":false,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":true,"ca_institutions":"","funders":"","keywords":"Oxygenation; Ventilation (architecture); Medicine; Growth hormone; Internal medicine; Cardiology; Hormone","score_opus":0.008769696045770952,"score_gpt":0.2270032696700938,"score_spread":0.21823357362432283,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4404090810","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99899083,0.00031296036,0.000040287916,0.00003122727,0.000006953447,0.0000074347613,0.00030100148,0.0000039960614,0.00030537788],"genre_scores_gemma":[0.9992673,0.00013908595,0.00006723467,0.00002904574,0.000014151308,0.000011799934,0.0004059773,0.0000018577477,0.000063479674],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99975365,0.000034611305,0.000030060182,0.00006537188,0.000053915475,0.00006245769],"domain_scores_gemma":[0.99923897,0.00017577907,0.0003254876,0.000031506857,0.000050685194,0.00017753353],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00023800509,0.0003208114,0.0003726677,0.0007284092,0.00027119392,0.00030890448,0.00023176773,0.00046963542,0.0014115436],"category_scores_gemma":[0.0014422786,0.00015894798,0.00033326543,0.0006008533,0.0003238558,0.0004529251,0.0003049402,0.0005918584,0.00023465118],"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":[0.00016983184,0.000033946453,0.99672335,0.000014024897,0.000017825003,0.0013514748,0.00006425786,0.00003787914,0.0004815949,0.000012291788,0.00007777812,0.0010156338],"study_design_scores_gemma":[0.000009067223,0.00033593568,0.9949462,0.0000058756277,0.000015462027,0.004180397,0.00015391989,0.000078164325,0.00014118233,0.000010652709,0.00011966436,0.0000034957527],"about_ca_topic_score_codex":0.0034329498,"about_ca_topic_score_gemma":0.0025722526,"teacher_disagreement_score":0.0034329498,"about_ca_system_score_codex":0.00044312276,"about_ca_system_score_gemma":0.00034555036,"threshold_uncertainty_score":0.0068259835},"labels":[],"label_agreement":null},{"id":"W4404318525","doi":"10.1136/jmg-2024-110115","title":"Long-read sequencing for detection and subtyping of Prader-Willi and Angelman syndromes","year":2024,"lang":"en","type":"article","venue":"Journal of Medical Genetics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","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":"University of Toronto; BC Children's Hospital; Hospital for Sick Children; Canada's Michael Smith Genome Sciences Centre; University of British Columbia","funders":"Canadian Institutes of Health Research; Canada Research Chairs; BC Cancer Agency; Simons Foundation Autism Research Initiative; BC Children's Hospital","keywords":"Subtyping; Angelman syndrome; Proband; Genetics; Genomic imprinting; Biology; Uniparental disomy; Multiplex ligation-dependent probe amplification; Computational biology; DNA methylation; Mutation; Computer science; Gene; Exon; Karyotype; Chromosome","score_opus":0.022827214892635048,"score_gpt":0.2930482432374433,"score_spread":0.2702210283448082,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4404318525","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9282079,0.0034879267,0.06213044,0.00034075155,0.00011727312,0.00014410073,0.0024191563,0.0004949853,0.0026574926],"genre_scores_gemma":[0.93251747,0.0009533726,0.06310438,0.00038124813,0.000045780478,0.00011962481,0.0015414081,0.00007070483,0.0012660923],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.999278,0.00016656576,0.000054757784,0.00026661207,0.00017217382,0.000061859515],"domain_scores_gemma":[0.99929106,0.00026435463,0.00014909824,0.00008209891,0.00013606294,0.0000772335],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0006335093,0.00035942128,0.00032047727,0.00094008894,0.00019809842,0.00043487194,0.00036571515,0.00051145797,0.0007506537],"category_scores_gemma":[0.0017277581,0.00015657903,0.0003006519,0.00039333123,0.00019239345,0.000250546,0.00041751133,0.0004526769,0.00029929515],"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":[0.0005810153,0.00014985111,0.14060354,0.0003268757,0.000266511,0.0022052887,0.0006872612,0.0022828057,0.76029634,0.0011166931,0.0013207073,0.09016308],"study_design_scores_gemma":[0.00007409581,0.0010488405,0.40323615,0.00024045468,0.0004928275,0.013626568,0.0008500715,0.054887764,0.49877217,0.0034834752,0.023170507,0.000116981566],"about_ca_topic_score_codex":0.0009864935,"about_ca_topic_score_gemma":0.003945375,"teacher_disagreement_score":0.0009864935,"about_ca_system_score_codex":0.00024218664,"about_ca_system_score_gemma":0.00021662997,"threshold_uncertainty_score":0.003350377},"labels":[],"label_agreement":null},{"id":"W4404867725","doi":"10.1515/med-2024-1058","title":"A bibliometric analysis of Prader-Willi syndrome from 2002 to 2022","year":2024,"lang":"en","type":"article","venue":"Open Medicine","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":1,"is_retracted":false,"has_abstract":true,"route_ca_aff":false,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":true,"ca_institutions":"","funders":"","keywords":"Medicine; Web of science; Citation; Library science; Pathology; Meta-analysis","score_opus":0.023543982914768582,"score_gpt":0.32062748842251615,"score_spread":0.2970835055077476,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4404867725","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":[0.2829734,0.33373085,0.0014205197,0.0057801795,0.0006826963,0.0009353568,0.3543534,0.0006234062,0.019500224],"genre_scores_gemma":[0.65507686,0.19835725,0.0037407803,0.00069833413,0.00095013704,0.0017411972,0.1363105,0.00012582098,0.0029991327],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9851896,0.0019835671,0.00473392,0.0015087046,0.0059585753,0.0006255449],"domain_scores_gemma":[0.9426492,0.025866201,0.014490326,0.0011360747,0.014526757,0.0013314905],"candidate_categories":["bibliometrics"],"consensus_categories":[],"category_scores_codex":[0.006681528,0.0010212829,0.0033346275,0.19227634,0.0011288191,0.0049282736,0.0012733187,0.0012311906,0.005495544],"category_scores_gemma":[0.043144934,0.00042039325,0.0034874934,0.23366898,0.0006801148,0.0035331792,0.0019046266,0.0007051653,0.0011622366],"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":[0.0010962054,0.00023182966,0.4978276,0.13612266,0.008234484,0.0021771,0.002913311,0.0032545025,0.0015822442,0.0032150205,0.06396125,0.27938372],"study_design_scores_gemma":[0.00015458865,0.00027728925,0.857663,0.021279491,0.007987667,0.0027892115,0.0034634012,0.0034813378,0.0009712677,0.0015746104,0.100176916,0.00018114864],"about_ca_topic_score_codex":0.014876187,"about_ca_topic_score_gemma":0.012917566,"teacher_disagreement_score":0.80772364,"about_ca_system_score_codex":0.0045779585,"about_ca_system_score_gemma":0.0071419673,"threshold_uncertainty_score":0.03533572},"labels":[],"label_agreement":null},{"id":"W4405422020","doi":"10.1002/ajmg.a.63961","title":"Community‐Sourced Reporting of Mortalities in Angelman Syndrome (1979–2022)","year":2024,"lang":"en","type":"article","venue":"American Journal of Medical Genetics Part A","topic":"Genetic Syndromes and Imprinting","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":"Pierre Elliott Trudeau Foundation","funders":"National Center for Research Resources; Ionis Pharmaceuticals; Eunice Kennedy Shriver National Institute of Child Health and Human Development; Ultragenyx Pharmaceutical","keywords":"Medicine; Epilepsy; Population; Life expectancy; Incidence (geometry); Epidemiology; Angelman syndrome; Psychiatry; Pediatrics; Sudden infant death syndrome; Public health; Demography; Gerontology; Environmental health; Pathology","score_opus":0.024672327748454365,"score_gpt":0.31726265589703473,"score_spread":0.2925903281485804,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4405422020","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.6724266,0.003301226,0.00065295026,0.0010169864,0.00039637406,0.00024513277,0.30239353,0.00023263105,0.019334666],"genre_scores_gemma":[0.7658923,0.0038942,0.0014956715,0.00086351245,0.00037686474,0.00060699024,0.21768968,0.000090916736,0.009089759],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99897885,0.00014403852,0.00026690314,0.00014412178,0.00036524536,0.00010091295],"domain_scores_gemma":[0.9927362,0.0007550231,0.0032554644,0.00033046262,0.002241898,0.0006809236],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0012269089,0.00031015745,0.00021608967,0.00514014,0.00044457996,0.00047803312,0.00054299977,0.00040335002,0.0032909003],"category_scores_gemma":[0.0060121664,0.00019280738,0.00037404516,0.0036641103,0.0001903988,0.00039198648,0.00093326176,0.0004083091,0.0011924038],"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":[0.00019592316,0.00004286844,0.936225,0.0005267167,0.0001770668,0.00064724387,0.00061851356,0.000082885614,0.00091577607,0.00017794064,0.0398729,0.020517167],"study_design_scores_gemma":[0.000010981175,0.000028827631,0.98736215,0.00014777035,0.00003900873,0.00056924624,0.00041650483,0.00011769948,0.00034705858,0.000036592573,0.010902903,0.000021219097],"about_ca_topic_score_codex":0.07870983,"about_ca_topic_score_gemma":0.086052194,"teacher_disagreement_score":0.07870983,"about_ca_system_score_codex":0.00082132174,"about_ca_system_score_gemma":0.00093733915,"threshold_uncertainty_score":0.15650338},"labels":[],"label_agreement":null},{"id":"W4405422616","doi":"10.1186/s12916-024-03804-2","title":"Cognitive benefits of folic acid supplementation during pregnancy track with epigenetic changes at an imprint regulator","year":2024,"lang":"en","type":"article","venue":"BMC Medicine","topic":"Genetic Syndromes and Imprinting","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":"University of British Columbia","funders":"Economic and Social Research Council; Biotechnology and Biological Sciences Research Council; Directorate for Biological Sciences; Linköpings Universitet","keywords":"DNA methylation; Methylation; Epigenetics; Genetics; Biology; Pyrosequencing; Genomic imprinting; Differentially methylated regions; Methyltransferase; Quantitative trait locus; Gene; Gene expression","score_opus":0.0224369532210712,"score_gpt":0.28216838151881024,"score_spread":0.25973142829773904,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4405422616","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99533737,0.0028050968,0.00065341924,0.00021867001,0.000030094167,0.000032064538,0.00031421587,0.000017578432,0.0005914793],"genre_scores_gemma":[0.9971738,0.0010535647,0.00097605947,0.00008926186,0.000014286706,0.00005888831,0.00018429213,0.0000048451175,0.00044508473],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9998648,0.000050882674,0.000011472248,0.000027379338,0.000025701873,0.000019735537],"domain_scores_gemma":[0.9996642,0.00013533917,0.00009259737,0.000042647323,0.000026743528,0.00003850264],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0003780718,0.00016827752,0.00029858947,0.00013448259,0.0001194847,0.00018531283,0.00013278174,0.0002468539,0.0013558232],"category_scores_gemma":[0.0010399132,0.00007391183,0.00020140935,0.00012751466,0.00022724955,0.00008361221,0.00015647216,0.00034508144,0.00007113273],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.09992717,0.0022892444,0.09511397,0.0013298247,0.0012903068,0.00069800834,0.0005846072,0.0007180402,0.61075,0.0005423516,0.0010637015,0.18569276],"study_design_scores_gemma":[0.0043726615,0.0642583,0.7085469,0.00033656642,0.0040170304,0.0016674178,0.00038692163,0.0014885241,0.20066184,0.0014788995,0.012743581,0.00004145493],"about_ca_topic_score_codex":0.0012266069,"about_ca_topic_score_gemma":0.001112369,"teacher_disagreement_score":0.0013558232,"about_ca_system_score_codex":0.00020789598,"about_ca_system_score_gemma":0.00032414278,"threshold_uncertainty_score":0.004535675},"labels":[],"label_agreement":null},{"id":"W4406139981","doi":"10.1136/ebnurs-2024-104171","title":"Evaluating psychiatric care for people with Prader-Willi syndrome","year":2025,"lang":"en","type":"article","venue":"Evidence-Based Nursing","topic":"Genetic Syndromes and Imprinting","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":"Athabasca University; University of Alberta","funders":"","keywords":"Psychiatry; Psychology; Medicine","score_opus":0.02627206680414197,"score_gpt":0.33837608166813,"score_spread":0.31210401486398803,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4406139981","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":[0.9177822,0.008931426,0.0014950914,0.035206296,0.0010135415,0.00041055167,0.0001853055,0.00006916896,0.034906454],"genre_scores_gemma":[0.9830683,0.006182434,0.0046905954,0.0038688611,0.00026139207,0.00011190965,0.00008226023,0.00001208456,0.0017222672],"study_design_codex":"observational","study_design_gemma":"systematic_review","domain_scores_codex":[0.9987375,0.00063788774,0.00017280578,0.000048558562,0.00022754633,0.00017576896],"domain_scores_gemma":[0.99678373,0.00095861795,0.00060644414,0.000045735676,0.0006513546,0.0009540523],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0014409471,0.00021996933,0.00034946424,0.0006145123,0.0017606072,0.0010223537,0.000721635,0.0008282342,0.0018927122],"category_scores_gemma":[0.011293201,0.0001562652,0.0003214819,0.00033140086,0.0005142172,0.0006522074,0.0014074931,0.0014262749,0.00025359265],"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":[0.00028557007,0.001490323,0.69452065,0.0012698818,0.00018959893,0.014802991,0.015180555,0.0008773666,0.00125387,0.0007950224,0.02494666,0.24438748],"study_design_scores_gemma":[0.00026484887,0.002869978,0.76851356,0.005484624,0.00049917476,0.033335865,0.1398183,0.0031429832,0.0023823539,0.008114608,0.03535642,0.00021740278],"about_ca_topic_score_codex":0.005973089,"about_ca_topic_score_gemma":0.020088518,"teacher_disagreement_score":0.005973089,"about_ca_system_score_codex":0.0014586964,"about_ca_system_score_gemma":0.0037498286,"threshold_uncertainty_score":0.011876643},"labels":[],"label_agreement":null},{"id":"W4406169200","doi":"10.1097/scs.0000000000011045","title":"Outcomes of Tongue Reduction Surgery in Beckwith-Wiedemann Syndrome: A Systematic Review","year":2025,"lang":"en","type":"review","venue":"Journal of Craniofacial Surgery","topic":"Genetic Syndromes and Imprinting","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":"Izaak Walton Killam Health Centre; Dalhousie University","funders":"","keywords":"Macroglossia; Medicine; Beckwith–Wiedemann syndrome; Glossectomy; Tongue; Surgery; Drooling","score_opus":0.024410323628179156,"score_gpt":0.3075404588100349,"score_spread":0.28313013518185576,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4406169200","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":[0.0031366572,0.9955836,0.00006902488,0.00017497645,0.000053922733,0.00016483528,0.0005986703,0.000005790957,0.00021258646],"genre_scores_gemma":[0.05530864,0.9424812,0.00042316644,0.0005299027,0.00008171878,0.000559921,0.00050474255,0.0000060661414,0.00010461475],"study_design_codex":"systematic_review","study_design_gemma":"systematic_review","domain_scores_codex":[0.9953413,0.0013377508,0.001884165,0.0004747635,0.00077750126,0.00018455954],"domain_scores_gemma":[0.9837542,0.0109401215,0.0037715856,0.00019709137,0.001125543,0.00021141532],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0041754935,0.0011247708,0.0071902364,0.0059825643,0.0004994379,0.002127723,0.0015241121,0.0016547864,0.0034484991],"category_scores_gemma":[0.02302018,0.00074229285,0.0074495957,0.0066539943,0.0006394367,0.0014223503,0.0011751305,0.00087748247,0.00018402883],"study_design_candidate":"systematic_review","study_design_consensus":"systematic_review","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0003467704,0.000014510726,0.0022791305,0.96244365,0.014885081,0.000098206074,0.0001546154,0.00008872416,0.00009943659,0.00011702881,0.000890363,0.018582553],"study_design_scores_gemma":[0.00046349113,0.00034373187,0.015115759,0.83083,0.14228179,0.0005489167,0.00038124996,0.00013332984,0.00016343316,0.00028636304,0.009401512,0.000050472696],"about_ca_topic_score_codex":0.007932213,"about_ca_topic_score_gemma":0.019066751,"teacher_disagreement_score":0.007932213,"about_ca_system_score_codex":0.002475399,"about_ca_system_score_gemma":0.005968615,"threshold_uncertainty_score":0.022082388},"labels":[],"label_agreement":null},{"id":"W4406465014","doi":"10.1016/j.ajhg.2024.12.020","title":"Discovery of a DNA methylation profile in individuals with Sifrim-Hitz-Weiss syndrome","year":2025,"lang":"en","type":"article","venue":"The American Journal of Human Genetics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":6,"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; London Health Sciences Centre","funders":"Ministerie van Onderwijs, Cultuur en Wetenschap; Government of Canada; Ontario Genomics; Ontario Genomics Institute; Genome Canada","keywords":"DNA methylation; Genetics; Methylation; Computational biology; Biology; DNA; Psychology; Gene; Gene expression","score_opus":0.00852832446146463,"score_gpt":0.26459059037541943,"score_spread":0.2560622659139548,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4406465014","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9985904,0.00010233265,0.00045381222,0.00006827142,0.000007736708,0.0000075226694,0.00017885688,0.00002671274,0.0005642228],"genre_scores_gemma":[0.99935514,0.000029985194,0.00027438044,0.000024203564,0.0000065485783,0.0000033435224,0.00006498704,0.000005464929,0.00023582933],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99983,0.000020324265,0.000019375137,0.00005329619,0.0000425254,0.00003432156],"domain_scores_gemma":[0.99973744,0.000076514254,0.00006597627,0.00002088357,0.000033862674,0.00006526169],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00015979243,0.0005157553,0.0002983203,0.0018312548,0.00043565469,0.0002836523,0.00030504254,0.00054268027,0.0018083001],"category_scores_gemma":[0.0010171196,0.00019050195,0.00024429313,0.0006135792,0.0002656993,0.00015200027,0.0002592618,0.00029306562,0.00024947192],"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":[0.00087343383,0.00010096143,0.5946305,0.000055918663,0.00014334972,0.041675083,0.0012930052,0.0002915047,0.34607288,0.00038385086,0.000398658,0.014080814],"study_design_scores_gemma":[0.00002273472,0.00038158806,0.9057581,0.000012607654,0.00016768463,0.06378718,0.000578581,0.0010666886,0.026645906,0.00029521127,0.0012605065,0.000023204335],"about_ca_topic_score_codex":0.0023303707,"about_ca_topic_score_gemma":0.0022793,"teacher_disagreement_score":0.0023303707,"about_ca_system_score_codex":0.00017190249,"about_ca_system_score_gemma":0.00012864853,"threshold_uncertainty_score":0.006049335},"labels":[],"label_agreement":null},{"id":"W4406547971","doi":"10.1016/j.yobg.2013.05.021","title":"10.1016/j.yobg.2013.05.021","year":2000,"lang":"en","type":"article","venue":"Time to knit","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":0,"is_retracted":false,"has_abstract":false,"route_ca_aff":false,"route_ca_fund":false,"route_ca_venue":true,"route_about_ca":false,"ca_institutions":"","funders":"","keywords":"Intracytoplasmic sperm injection; Medicine; In vitro fertilisation; Imprinting (psychology); Andrology; Human fertilization; Sperm; Embryo; Cell biology; Anatomy; Genetics; Biology; Gene","score_opus":0.004542760661689865,"score_gpt":0.1786053454299288,"score_spread":0.17406258476823894,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4406547971","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":[0.0062937182,0.019958654,0.0032438603,0.010261943,0.0025447141,0.00008831394,0.0038563074,0.0017378307,0.9520145],"genre_scores_gemma":[0.01179754,0.0055507305,0.0020556466,0.0020767117,0.00060243614,0.000061028426,0.0019993486,0.00027035928,0.9755862],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.9998443,0.000012048805,0.00000889919,0.00004976813,0.00004404383,0.000040824652],"domain_scores_gemma":[0.999476,0.000073795745,0.0000609252,0.0000313105,0.000093404786,0.00026455618],"candidate_categories":["insufficient_payload"],"consensus_categories":["insufficient_payload"],"category_scores_codex":[0.00046770927,0.001089167,0.00061357213,0.001074471,0.0009472395,0.0021657106,0.0009136217,0.003079895,0.8801601],"category_scores_gemma":[0.0006740983,0.00041830173,0.00049453066,0.00062115653,0.0008557037,0.0017138933,0.0011024232,0.0015916472,0.8219165],"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":[0.00046025641,0.00023671417,0.0034146465,0.00047142236,0.000043768017,0.00057524024,0.00011075963,0.00021987372,0.002670028,0.008802887,0.28704855,0.69594586],"study_design_scores_gemma":[0.00006597607,0.00010976916,0.004904099,0.0005374205,0.000034460805,0.002124987,0.00018201205,0.0001754061,0.00073720934,0.0053892075,0.9857143,0.000025103236],"about_ca_topic_score_codex":0.0023626282,"about_ca_topic_score_gemma":0.0021900286,"teacher_disagreement_score":0.11983991,"about_ca_system_score_codex":0.00069565,"about_ca_system_score_gemma":0.0009460007,"threshold_uncertainty_score":0.170937},"labels":[],"label_agreement":null},{"id":"W4406644320","doi":"10.1007/s12519-024-00865-4","title":"Sex dimorphic associations of Prader–Willi imprinted gene expressions in umbilical cord with prenatal and postnatal growth in healthy infants","year":2025,"lang":"en","type":"article","venue":"World Journal of Pediatrics","topic":"Genetic Syndromes and Imprinting","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":"University of Alberta","funders":"Centro de Investigación Biomédica en Red Diabetes y Enfermedades Metabólicas Asociadas; Instituto de Salud Carlos III; Ministerio de Ciencia e Innovación; European Regional Development Fund; Generalitat Valenciana; Asociación Española de Pediatría","keywords":"Umbilical cord; Sexual dimorphism; Medicine; Birth weight; Fetus; Gene expression; Genomic imprinting; Gene; Endocrinology; Physiology; Internal medicine; Pregnancy; Biology; Genetics; Immunology; DNA methylation","score_opus":0.008866216166149948,"score_gpt":0.26644502545546084,"score_spread":0.2575788092893109,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4406644320","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.999416,0.00022891849,0.00012891483,0.0000043247146,0.0000011372821,0.0000012501016,0.00011209783,0.0000028197544,0.00010450281],"genre_scores_gemma":[0.9994717,0.00012999227,0.00016911849,0.000003915747,0.0000016892488,0.0000038085425,0.000118660755,0.0000028321285,0.00009834123],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9998764,0.000027429469,0.000011589959,0.00004303224,0.000022119582,0.0000194002],"domain_scores_gemma":[0.9995316,0.00014467539,0.00020364496,0.000032378965,0.000043165757,0.00004459017],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00017489401,0.00014594312,0.00013549649,0.00042051807,0.00007560352,0.00017878591,0.00012917662,0.000118887016,0.0007271909],"category_scores_gemma":[0.00084496883,0.000089340734,0.0001049327,0.00026222682,0.000176717,0.00008911542,0.00014229598,0.00012978035,0.0000879982],"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":[0.00065843284,0.00001638554,0.9482687,0.000028634095,0.000042297186,0.00032802878,0.0001490283,0.00007328266,0.043862175,0.00004235414,0.000033083354,0.0064975447],"study_design_scores_gemma":[0.0000014143534,0.00005355721,0.996198,0.0000024048502,0.000008477773,0.00038527907,0.00004074076,0.000107240914,0.0031185574,0.0000179059,0.00006495675,0.0000015623666],"about_ca_topic_score_codex":0.00084688765,"about_ca_topic_score_gemma":0.00072966254,"teacher_disagreement_score":0.00084688765,"about_ca_system_score_codex":0.00011881142,"about_ca_system_score_gemma":0.000059470938,"threshold_uncertainty_score":0.0024326444},"labels":[],"label_agreement":null},{"id":"W4406645055","doi":"10.1016/b978-84-8086-959-1.00566-6","title":"10.1016/b978-84-8086-959-1.00566-6","year":2000,"lang":"en","type":"book-chapter","venue":"Time to knit","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":0,"is_retracted":false,"has_abstract":false,"route_ca_aff":false,"route_ca_fund":false,"route_ca_venue":true,"route_about_ca":false,"ca_institutions":"","funders":"","keywords":"Medicine; Dermatology","score_opus":0.0064289515322694495,"score_gpt":0.17671278670579396,"score_spread":0.17028383517352452,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4406645055","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":[0.00025141163,0.0011826972,0.0012042855,0.00040932,0.00028725146,0.00006537819,0.00084751257,0.0010342043,0.994718],"genre_scores_gemma":[0.0005561166,0.00058554765,0.0005214376,0.00015555506,0.00006365164,0.000051134848,0.00051974517,0.00020501082,0.99734193],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.9995654,0.000025438996,0.00003206242,0.00015729268,0.00013021693,0.000089497706],"domain_scores_gemma":[0.99832994,0.0005911998,0.00012506833,0.00018509958,0.00025269535,0.0005159864],"candidate_categories":["insufficient_payload"],"consensus_categories":["insufficient_payload"],"category_scores_codex":[0.0009659997,0.002668435,0.0018415494,0.0018972704,0.001308283,0.004250286,0.003169677,0.00447628,0.97728527],"category_scores_gemma":[0.0014119247,0.0008480456,0.0010334074,0.0018622963,0.0013398681,0.0048585725,0.0031320564,0.0026762316,0.9889642],"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":[0.00023018665,0.00015044429,0.00031961256,0.0005815961,0.000025779402,0.00016338674,0.00008904115,0.00041258216,0.0034476933,0.006130992,0.32588577,0.6625629],"study_design_scores_gemma":[0.000029299803,0.00005729843,0.0005318511,0.0003418284,0.00001105442,0.0003090018,0.00007982748,0.00012771672,0.00044326863,0.0013142612,0.99673754,0.000017026068],"about_ca_topic_score_codex":0.002566315,"about_ca_topic_score_gemma":0.002177214,"teacher_disagreement_score":0.022714734,"about_ca_system_score_codex":0.00086623355,"about_ca_system_score_gemma":0.0007921231,"threshold_uncertainty_score":0.032399714},"labels":[],"label_agreement":null},{"id":"W4408007158","doi":"10.1101/2025.02.25.25322869","title":"Neurophysiological dysconnectivity across multiple resting state brain networks and cognitive impairment in children with Prader-Willi Syndrome","year":2025,"lang":"en","type":"preprint","venue":"medRxiv","topic":"Genetic Syndromes and Imprinting","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":"Holland Bloorview Kids Rehabilitation Hospital; Western University; Mental Health Research Canada; Hospital for Sick Children; Toronto Rehabilitation Institute; University of Toronto","funders":"","keywords":"Neurophysiology; Cognitive impairment; Neuroscience; Cognition; Resting state fMRI; Psychology; Functional connectivity","score_opus":0.010606764872508511,"score_gpt":0.2566367630351931,"score_spread":0.24602999816268462,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4408007158","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99951017,0.000040404382,0.0001756927,0.000021414184,0.0000018834788,0.0000067538667,0.00012392369,0.0000071386908,0.000112577756],"genre_scores_gemma":[0.9993432,0.00005731612,0.00035160253,0.0000124915305,0.0000038187227,0.00002077716,0.00012004107,0.00000463115,0.00008607451],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.999671,0.00006982581,0.000031679083,0.00011802783,0.00006821246,0.00004133915],"domain_scores_gemma":[0.99914896,0.00025433357,0.00039119934,0.00005808895,0.000057038797,0.000090445144],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0005073132,0.0006000126,0.00031817757,0.0010285724,0.00027630775,0.00042253584,0.000289565,0.00034320494,0.0017269966],"category_scores_gemma":[0.0018777354,0.00021888976,0.00023458363,0.00044215017,0.00060477277,0.00037898205,0.00064143835,0.00049646804,0.00013021074],"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":[0.0003538939,0.00016557088,0.96811074,0.00006348733,0.00010438134,0.0040704478,0.00083047705,0.00029102192,0.0197738,0.00013702139,0.00017030582,0.0059289006],"study_design_scores_gemma":[0.0000061624946,0.00012981793,0.9964515,0.000005889284,0.000015535608,0.0022826525,0.0001720205,0.00017765969,0.000633657,0.000049055587,0.00007186505,0.000004187498],"about_ca_topic_score_codex":0.003139496,"about_ca_topic_score_gemma":0.0033493633,"teacher_disagreement_score":0.003139496,"about_ca_system_score_codex":0.00024695936,"about_ca_system_score_gemma":0.0002830855,"threshold_uncertainty_score":0.006242454},"labels":[],"label_agreement":null},{"id":"W4408128735","doi":"10.1210/clinem/dgaf142","title":"Fiber Intervention Study in Prader-Willi Syndrome: Insights into Metabolic and Microbiota Shifts","year":2025,"lang":"en","type":"article","venue":"The Journal of Clinical Endocrinology & Metabolism","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":1,"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; University of Alberta","funders":"Chinese University of Hong Kong; Weston Family Foundation","keywords":"Crossover study; Randomized controlled trial; Fiber; Intervention (counseling); Crossover; Medicine; Biology; Internal medicine; Computer science; Materials science; Alternative medicine; Nursing; Composite material; Pathology; Artificial intelligence","score_opus":0.01961927069978049,"score_gpt":0.3457885065733603,"score_spread":0.3261692358735798,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4408128735","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9982926,0.0009346474,0.00021259424,0.00009606483,0.00002194355,0.0001549167,0.000074547075,0.0000066025304,0.00020613182],"genre_scores_gemma":[0.99564433,0.0013300246,0.001476,0.00018930582,0.000029330144,0.00040900082,0.00017411602,0.000003415215,0.00074445386],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99961925,0.00020695114,0.000032675795,0.000062035324,0.00004097896,0.000038111306],"domain_scores_gemma":[0.99957734,0.000089418754,0.00009306072,0.00003910464,0.000054986733,0.00014615981],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0010119105,0.00056505296,0.0006204075,0.00023856969,0.0003242531,0.00022061185,0.00018073163,0.00048377088,0.0016657353],"category_scores_gemma":[0.00077750563,0.00016219869,0.00053896336,0.00020860604,0.00028704613,0.00023886809,0.00045567108,0.0004916176,0.00012379316],"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":[0.2739973,0.047426064,0.2887572,0.0029342135,0.00691997,0.0013546611,0.0014631309,0.00076857774,0.1228101,0.00046378828,0.0011015753,0.25200343],"study_design_scores_gemma":[0.016895602,0.24454531,0.7196543,0.00032356608,0.0024459027,0.00064616796,0.00053723,0.0007592236,0.009811399,0.00023893468,0.004095862,0.00004655689],"about_ca_topic_score_codex":0.0019428061,"about_ca_topic_score_gemma":0.004101643,"teacher_disagreement_score":0.0019428061,"about_ca_system_score_codex":0.00030702096,"about_ca_system_score_gemma":0.00075621443,"threshold_uncertainty_score":0.0055724382},"labels":[],"label_agreement":null},{"id":"W4408717504","doi":"10.5664/jcsm.11664","title":"Personalized endpoints in Prader-Willi syndrome: a case study with goal attainment scaling","year":2025,"lang":"en","type":"article","venue":"Journal of Clinical Sleep Medicine","topic":"Genetic Syndromes and Imprinting","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":"Nova Scotia Health Authority; Dalhousie University","funders":"","keywords":"Medicine; Goal Attainment Scaling; Physical medicine and rehabilitation; Physical therapy","score_opus":0.02838142673211102,"score_gpt":0.380721298490769,"score_spread":0.352339871758658,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4408717504","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.983851,0.00061711215,0.0038335077,0.0023477983,0.00007802795,0.00014025357,0.00012778382,0.00005018127,0.008954357],"genre_scores_gemma":[0.995378,0.00033883727,0.0021130196,0.00019443422,0.000031732554,0.000029317016,0.000036973655,0.000021386715,0.0018563609],"study_design_codex":"case_report","study_design_gemma":"case_report","domain_scores_codex":[0.99929655,0.00024230979,0.00006557909,0.0001227052,0.00016838034,0.00010444738],"domain_scores_gemma":[0.9978764,0.0012317303,0.00030369908,0.00014995404,0.000119325625,0.00031891558],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0008363282,0.00077202235,0.00061359024,0.0009349359,0.0020651508,0.0010377127,0.0008078006,0.0014943115,0.0021888898],"category_scores_gemma":[0.0064079883,0.00023944202,0.0006520418,0.0009053456,0.0014021544,0.0006653636,0.0013956511,0.0022655204,0.00021926158],"study_design_candidate":"case_report","study_design_consensus":"case_report","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00016935822,0.00054749905,0.06700798,0.00007495306,0.000044557284,0.8995226,0.004736673,0.0005576328,0.0012054148,0.0069946097,0.00095104956,0.018187644],"study_design_scores_gemma":[0.000039991854,0.00050632196,0.0396392,0.00010138798,0.00007617559,0.9408352,0.004010267,0.004139471,0.0013828429,0.005618371,0.0035956511,0.00005501219],"about_ca_topic_score_codex":0.0046928343,"about_ca_topic_score_gemma":0.0037316883,"teacher_disagreement_score":0.0046928343,"about_ca_system_score_codex":0.0009911815,"about_ca_system_score_gemma":0.0010436176,"threshold_uncertainty_score":0.009330988},"labels":[],"label_agreement":null},{"id":"W4409058591","doi":"10.1101/2025.03.27.645693","title":"Identification of genetic and non-genetic modifiers of genomic imprinting through whole genome screening in humans","year":2025,"lang":"en","type":"preprint","venue":"bioRxiv (Cold Spring Harbor Laboratory)","topic":"Genetic Syndromes and Imprinting","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":"London Health Sciences Centre; Western University","funders":"","keywords":"Genomic imprinting; Identification (biology); Genetics; Biology; Genome; Computational biology; Gene; DNA methylation","score_opus":0.010503323862083018,"score_gpt":0.2263524698867477,"score_spread":0.21584914602466468,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4409058591","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.98516464,0.0016154408,0.009392441,0.00011057472,0.000009177433,0.000021970589,0.002631181,0.0001161154,0.0009385156],"genre_scores_gemma":[0.991799,0.0006249666,0.0055295075,0.00009520278,0.000011257426,0.000022592769,0.0013543217,0.000026140075,0.0005371624],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.99977154,0.000053440515,0.000013367699,0.00010385255,0.000039482464,0.000018340192],"domain_scores_gemma":[0.9998265,0.000069228874,0.00004386845,0.000032667802,0.00000876027,0.000019049727],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0003023628,0.00022231777,0.00030213318,0.00074108166,0.00014833423,0.00021959066,0.00017199118,0.0002607248,0.001362038],"category_scores_gemma":[0.00048630475,0.00014320509,0.00022039907,0.00050127984,0.00022253112,0.000088385306,0.00028965363,0.00022689751,0.00017769837],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0007515241,0.00006904234,0.27844173,0.0002396149,0.0005367962,0.0017102335,0.00037873,0.0011791606,0.6440268,0.001022083,0.0010832138,0.070561],"study_design_scores_gemma":[0.000041784948,0.00027765884,0.9252592,0.000031597203,0.00018066553,0.00493415,0.00008235948,0.0025445423,0.061343156,0.0010588372,0.0042239977,0.000021937041],"about_ca_topic_score_codex":0.0008316455,"about_ca_topic_score_gemma":0.0006831829,"teacher_disagreement_score":0.001362038,"about_ca_system_score_codex":0.00009556598,"about_ca_system_score_gemma":0.00010301613,"threshold_uncertainty_score":0.0045564175},"labels":[],"label_agreement":null},{"id":"W4409986288","doi":"10.1038/s41467-025-59109-2","title":"Allelic effects on KLHL17 expression underlie a pancreatic cancer genome-wide association signal at chr1p36.33","year":2025,"lang":"en","type":"article","venue":"Nature Communications","topic":"Genetic Syndromes and Imprinting","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":"Sinai Health System; Lunenfeld-Tanenbaum Research Institute; University of Toronto","funders":"Division of Cancer Epidemiology and Genetics, National Cancer Institute; National Heart, Lung, and Blood Institute; Medical Research Council; Centers for Disease Control and Prevention; National Cancer Institute; U.S. Department of Health and Human Services; National Institutes of Health; Cancer Research UK; Centre International de Recherche sur le Cancer; World Health Organization","keywords":"Pancreatic cancer; Allele; Genetics; Association (psychology); Biology; Genome; Cancer; Computational biology; Gene; Bioinformatics; Psychology","score_opus":0.008902243679664534,"score_gpt":0.28194286931593504,"score_spread":0.2730406256362705,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4409986288","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9957087,0.0003159458,0.0020576748,0.00014580076,0.000018668956,0.000008280807,0.0010306891,0.000084226944,0.0006300434],"genre_scores_gemma":[0.9980363,0.000089345376,0.00090414414,0.000048276972,0.0000074307395,0.000006026435,0.00034764825,0.000020236655,0.00054069655],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.99976104,0.000056740297,0.000018995925,0.00008360519,0.000049891525,0.000029683315],"domain_scores_gemma":[0.99960786,0.00012465815,0.00015872793,0.00003454031,0.00001658149,0.000057719597],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0002488391,0.00040078716,0.0002217741,0.0005757172,0.00019654456,0.00039582603,0.00023095991,0.00029965746,0.0061770747],"category_scores_gemma":[0.00058627484,0.00017286272,0.00048683907,0.00061363535,0.00023336514,0.00008431978,0.00033543262,0.00044026622,0.00038247564],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0026163543,0.00008815605,0.30291483,0.00017483589,0.0006054874,0.0033766623,0.00023830049,0.0009162414,0.6704149,0.0008392821,0.00082149985,0.016993517],"study_design_scores_gemma":[0.00007669779,0.00014510954,0.9621775,0.000021703203,0.0003429066,0.003770329,0.00009310422,0.0016859149,0.029059779,0.0006424449,0.0019665675,0.000017889499],"about_ca_topic_score_codex":0.0018272785,"about_ca_topic_score_gemma":0.0021752818,"teacher_disagreement_score":0.0061770747,"about_ca_system_score_codex":0.00015707008,"about_ca_system_score_gemma":0.00014157231,"threshold_uncertainty_score":0.020664334},"labels":[],"label_agreement":null},{"id":"W4410400129","doi":"10.7554/elife.94502.2","title":"Post-fertilization transcription initiation in an ancestral LTR retrotransposon drives lineage-specific genomic imprinting of ZDBF2","year":2025,"lang":"en","type":"preprint","venue":"eLife","topic":"Genetic Syndromes and Imprinting","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":"University of British Columbia","funders":"","keywords":"Retrotransposon; Genomic imprinting; Imprinting (psychology); Biology; Lineage (genetic); Genetics; Evolutionary biology; Genome; Gene; Transposable element; DNA methylation; Gene expression","score_opus":0.023738000150062555,"score_gpt":0.27654331456724995,"score_spread":0.2528053144171874,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4410400129","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9931131,0.0006594258,0.0040895394,0.000051087394,0.000020907342,0.000014841496,0.00043269037,0.000109151304,0.0015091586],"genre_scores_gemma":[0.9939162,0.00017186436,0.0018564006,0.000036686128,0.0000061440487,0.000009363599,0.00076602976,0.00003469523,0.0032026637],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.999881,0.000014555611,0.000006972957,0.00004470942,0.000024616567,0.000028007913],"domain_scores_gemma":[0.99991775,0.000020156505,0.000023754495,0.000010881525,0.0000071124427,0.000020356485],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00010591416,0.00019609102,0.000108242304,0.00018956969,0.00012871443,0.00020279583,0.00017002992,0.00020350631,0.0018862858],"category_scores_gemma":[0.000105253486,0.00014532074,0.00019064531,0.00008886788,0.00015682138,0.00010081864,0.00023106893,0.00037418175,0.0007437191],"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":[0.000026426085,0.000003641258,0.00025261185,0.000008512602,7.8012647e-7,0.000024902356,0.000012759773,0.00001130849,0.9990132,0.00006995491,0.00001575449,0.00055997586],"study_design_scores_gemma":[0.000020586973,0.00016274558,0.02301962,0.00001448596,0.000012186029,0.00049236434,0.00008763546,0.0014652027,0.9683108,0.00008211129,0.006324782,0.0000075028424],"about_ca_topic_score_codex":0.0005319204,"about_ca_topic_score_gemma":0.001427008,"teacher_disagreement_score":0.0018862858,"about_ca_system_score_codex":0.0002654451,"about_ca_system_score_gemma":0.00009153964,"threshold_uncertainty_score":0.0063102245},"labels":[],"label_agreement":null},{"id":"W4410513017","doi":"10.3899/jrheum.2025-0390.pv145a","title":"RHUPUS SYNDROME: DESCRIPTION OF CLINICAL MANIFESTATIONS, ANALYTICAL FINDINGS, AND THERAPEUTIC APPROACH IN A SERIES OF 10 CASES","year":2025,"lang":"en","type":"article","venue":"The Journal of Rheumatology","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":0,"is_retracted":false,"has_abstract":true,"route_ca_aff":false,"route_ca_fund":false,"route_ca_venue":true,"route_about_ca":false,"ca_institutions":"","funders":"","keywords":"Medicine; Series (stratigraphy); Intensive care medicine; Dermatology","score_opus":0.033455077217247484,"score_gpt":0.30994438929590884,"score_spread":0.27648931207866134,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4410513017","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99344,0.003350419,0.0008725183,0.000106316176,0.000038486884,0.000090138456,0.00011219379,0.00004147407,0.0019484608],"genre_scores_gemma":[0.997523,0.0011996399,0.0005736267,0.000088694105,0.00008044351,0.000055687437,0.00014145378,0.0000071062577,0.00033047266],"study_design_codex":"case_report","study_design_gemma":"case_report","domain_scores_codex":[0.99936837,0.00010477264,0.00010452903,0.00016006987,0.00007411631,0.00018821417],"domain_scores_gemma":[0.9991278,0.00018466613,0.00027792162,0.00007009643,0.000046762296,0.0002927671],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0003891399,0.0014804553,0.0006633729,0.002827373,0.0010342204,0.0009856932,0.00074525696,0.0013816975,0.0012894438],"category_scores_gemma":[0.0018631393,0.0007293848,0.00057120924,0.0016088462,0.001184676,0.00092573935,0.001109929,0.0006868463,0.00063583115],"study_design_candidate":"case_report","study_design_consensus":"case_report","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.000184065,0.00023127349,0.42505515,0.00010612264,0.000059041027,0.5558805,0.0012227421,0.00023522848,0.003234532,0.00021287502,0.000571657,0.013006977],"study_design_scores_gemma":[0.000025001116,0.00038984398,0.17003232,0.000030034802,0.00002986218,0.8266425,0.0007607474,0.00030827743,0.00055162515,0.00011973556,0.0010779753,0.00003197722],"about_ca_topic_score_codex":0.0011310617,"about_ca_topic_score_gemma":0.0008489175,"teacher_disagreement_score":0.002827373,"about_ca_system_score_codex":0.00067279703,"about_ca_system_score_gemma":0.00042483665,"threshold_uncertainty_score":0.004881561},"labels":[],"label_agreement":null},{"id":"W4410708037","doi":"10.1016/j.ssmqr.2025.100574","title":"Dietary care and familialisation of children with Prader-Willi syndrome","year":2025,"lang":"en","type":"article","venue":"SSM - Qualitative Research in Health","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":0,"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":"Fondation Maladies Rares; Taylor’s University; Rare Disease Foundation","keywords":"Pediatrics; Medicine; Psychology; Gerontology","score_opus":0.09358133874853918,"score_gpt":0.4812231762503912,"score_spread":0.387641837501852,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4410708037","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9990207,0.00033105878,0.00003560585,0.00008601285,0.000004252282,0.0000027436238,0.000023928817,0.000002275132,0.00049338746],"genre_scores_gemma":[0.9993449,0.00033212078,0.0001004606,0.00001694277,0.0000029182813,0.000004717849,0.000030631858,0.0000011000562,0.00016632545],"study_design_codex":"observational","study_design_gemma":"qualitative","domain_scores_codex":[0.99954695,0.00014352187,0.00003377367,0.0001160105,0.00007513746,0.00008463488],"domain_scores_gemma":[0.999368,0.00013098537,0.00033617744,0.000047874248,0.00004207598,0.000074945616],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0002788167,0.00028431375,0.00023971839,0.0009644851,0.0015466522,0.00057495304,0.0003497199,0.00031442748,0.0010369335],"category_scores_gemma":[0.0035067277,0.00021955234,0.0002319793,0.0007823212,0.0008910189,0.0003674102,0.0010838731,0.00047354095,0.00007582576],"study_design_candidate":"qualitative","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0001350659,0.00007044407,0.9158929,0.000079282654,0.00004023701,0.017932657,0.04672443,0.00016651492,0.0016970449,0.00065921136,0.0004642882,0.016137933],"study_design_scores_gemma":[0.000006394392,0.00015669041,0.93005365,0.00006557862,0.00003906792,0.028596252,0.03854795,0.00014194597,0.00034278052,0.00034400777,0.0016794077,0.000026193664],"about_ca_topic_score_codex":0.029391797,"about_ca_topic_score_gemma":0.04403193,"teacher_disagreement_score":0.029391797,"about_ca_system_score_codex":0.0012534286,"about_ca_system_score_gemma":0.0007877522,"threshold_uncertainty_score":0.05844146},"labels":[],"label_agreement":null},{"id":"W4410901524","doi":"10.1136/jmg-2024-110262","title":"Using long-read sequencing to detect and subtype a case with Temple syndrome","year":2025,"lang":"en","type":"article","venue":"Journal of Medical Genetics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":0,"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; BC Children's Hospital; University of British Columbia; Hospital for Sick Children; B.C. Women's Hospital & Health Centre; Canada's Michael Smith Genome Sciences Centre","funders":"Canadian Institutes of Health Research; Canada Research Chairs; BC Cancer Agency; BC Children's Hospital","keywords":"Genomic imprinting; Methylation; DNA methylation; Uniparental disomy; Biology; Multiplex; Genetics; Imprinting (psychology); Nanopore sequencing; Computational biology; Epigenomics; Differentially methylated regions; DNA sequencing; Chromosome; Gene; Karyotype","score_opus":0.029574987797891677,"score_gpt":0.31418456008569773,"score_spread":0.28460957228780603,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4410901524","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.97961915,0.0006147775,0.017084671,0.00031941707,0.00004581828,0.000060484635,0.0001389914,0.00018615324,0.0019306008],"genre_scores_gemma":[0.9799936,0.0002897884,0.018557684,0.00019292677,0.000023887353,0.000014355797,0.00018813423,0.000032184067,0.0007074485],"study_design_codex":"bench_or_experimental","study_design_gemma":"case_report","domain_scores_codex":[0.99970776,0.000026093658,0.000033537974,0.00010731803,0.000082878825,0.00004247801],"domain_scores_gemma":[0.99963117,0.00013965332,0.00006150952,0.00003469126,0.00005134101,0.00008166628],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00021207819,0.00041291185,0.00024826772,0.0010134411,0.00027657475,0.0003729147,0.00030266593,0.0009628072,0.0005547532],"category_scores_gemma":[0.0009138951,0.00017637106,0.0002565222,0.00022739693,0.00037431947,0.00034423303,0.0003824359,0.00045149284,0.00024407219],"study_design_candidate":"case_report","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00031028595,0.00010199712,0.085787944,0.00010756278,0.00006447808,0.24708399,0.0007278815,0.001384167,0.6271289,0.0006102297,0.00067363115,0.03601899],"study_design_scores_gemma":[0.00003282599,0.00043975803,0.089949585,0.00006626354,0.00019321537,0.5863436,0.00073647295,0.034203682,0.2802367,0.0017908929,0.0059398264,0.00006710163],"about_ca_topic_score_codex":0.0011260664,"about_ca_topic_score_gemma":0.0021599107,"teacher_disagreement_score":0.0011260664,"about_ca_system_score_codex":0.00021303435,"about_ca_system_score_gemma":0.00019635595,"threshold_uncertainty_score":0.0022389889},"labels":[],"label_agreement":null},{"id":"W4410954163","doi":"10.7554/elife.94502.3.sa4","title":"Author response: Post-fertilization transcription initiation in an ancestral LTR retrotransposon drives lineage-specific genomic imprinting of ZDBF2","year":2025,"lang":"en","type":"peer-review","venue":"","topic":"Genetic Syndromes and Imprinting","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","funders":"","keywords":"Retrotransposon; Genomic imprinting; Imprinting (psychology); Biology; Lineage (genetic); Genetics; Evolutionary biology; Gene; Genome; Transposable element; DNA methylation; Gene expression","score_opus":0.039182077467243795,"score_gpt":0.3219329710292623,"score_spread":0.28275089356201855,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4410954163","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":[0.10266241,0.0065160105,0.02725713,0.27687544,0.20505455,0.0009206024,0.013173509,0.00786978,0.35967058],"genre_scores_gemma":[0.11516629,0.0017994676,0.0045608906,0.009645787,0.0039517204,0.00007783725,0.00444137,0.000809535,0.8595472],"study_design_codex":"not_applicable","study_design_gemma":"not_applicable","domain_scores_codex":[0.9989729,0.0001303459,0.00004990252,0.00015120144,0.00057059777,0.00012508947],"domain_scores_gemma":[0.99590576,0.0009336869,0.00019935185,0.00028244773,0.0018781631,0.0008005391],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0013704078,0.0004210869,0.0004220011,0.00056930823,0.00085683743,0.0014920777,0.00068274036,0.0017766901,0.20802817],"category_scores_gemma":[0.0069990116,0.00025173198,0.0002146848,0.00034074284,0.0006359872,0.00063670654,0.0012437801,0.0013064812,0.054609105],"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":[0.001266356,0.00006410453,0.0039170817,0.000714806,0.000046760404,0.0022510528,0.0005779949,0.00077626243,0.11367933,0.012679494,0.79369074,0.07033601],"study_design_scores_gemma":[0.00009237545,0.000086863154,0.0058287447,0.000078563644,0.000014614803,0.0009373674,0.00065913575,0.0007508749,0.0424711,0.0021112277,0.94692427,0.00004484245],"about_ca_topic_score_codex":0.0018939556,"about_ca_topic_score_gemma":0.0043571456,"teacher_disagreement_score":0.20802817,"about_ca_system_score_codex":0.0010982247,"about_ca_system_score_gemma":0.0013984864,"threshold_uncertainty_score":0.69592357},"labels":[],"label_agreement":null},{"id":"W4410954493","doi":"10.7554/elife.94502.3","title":"Post-fertilization transcription initiation in an ancestral LTR retrotransposon drives lineage-specific genomic imprinting of ZDBF2","year":2025,"lang":"en","type":"article","venue":"eLife","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":0,"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":"Japan Society for the Promotion of Science; Canadian Institutes of Health Research; Mitsubishi Foundation; Takeda Science Foundation","keywords":"Retrotransposon; Genomic imprinting; Biology; Imprinting (psychology); Genetics; Lineage (genetic); Evolutionary biology; Genome; Gene; Transposable element; DNA methylation; Gene expression","score_opus":0.015134527507421214,"score_gpt":0.2638693933611692,"score_spread":0.248734865853748,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4410954493","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9953746,0.00044568762,0.0024771313,0.00003359605,0.000009085847,0.000009028846,0.00017403183,0.000059278984,0.0014174943],"genre_scores_gemma":[0.99607986,0.00017583335,0.0011511511,0.000024630846,0.0000037248278,0.000005539005,0.0003376871,0.00001800971,0.0022036564],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9999044,0.000012964815,0.0000058914534,0.000032815737,0.000020939511,0.000022966082],"domain_scores_gemma":[0.99992824,0.000017181404,0.000022923827,0.0000107985215,0.000006539068,0.000014321853],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00011533333,0.00015100765,0.00009600459,0.00016880463,0.00013140078,0.0001793957,0.00015452935,0.00015861217,0.0010497286],"category_scores_gemma":[0.0001239875,0.00013733919,0.0001529196,0.00008963668,0.00015154613,0.00009886062,0.00021730644,0.00028696732,0.00045787642],"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":[0.000030471861,0.0000028349516,0.00048673537,0.000008267787,9.895457e-7,0.00005040503,0.000028082703,0.0000161638,0.9982292,0.00011106808,0.0000134923075,0.0010223609],"study_design_scores_gemma":[0.000026372352,0.00017574955,0.044181116,0.00001531006,0.000019176563,0.0008405923,0.00013691383,0.0016386769,0.94428813,0.00010021025,0.008568707,0.000009153186],"about_ca_topic_score_codex":0.0006981059,"about_ca_topic_score_gemma":0.0018412601,"teacher_disagreement_score":0.0010497286,"about_ca_system_score_codex":0.00024314522,"about_ca_system_score_gemma":0.00012024375,"threshold_uncertainty_score":0.0035116673},"labels":[],"label_agreement":null},{"id":"W4411210085","doi":"10.1093/brain/awaf227","title":"Deciphering <i>DST</i> -associated disorders: biallelic variants affecting DST-b cause a congenital myopathy","year":2025,"lang":"en","type":"article","venue":"Brain","topic":"Genetic Syndromes and Imprinting","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":"Ottawa Hospital; Children's Hospital of Eastern Ontario; University of Ottawa","funders":"Else Kröner-Fresenius-Stiftung; Austrian Science Fund; Deutsche Forschungsgemeinschaft; Technische Universität München; Bundesministerium für Bildung und Forschung; Institute for Advanced Study","keywords":"Myopathy; Medicine; Genetics; Pathology; Biology","score_opus":0.00739109569379996,"score_gpt":0.24457897087131977,"score_spread":0.23718787517751982,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4411210085","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99766856,0.00046787589,0.0010204734,0.000060993283,0.00000814192,0.000008375071,0.00019671493,0.00002650725,0.0005424542],"genre_scores_gemma":[0.99767464,0.0003746862,0.0010934949,0.000054289918,0.000015527983,0.0000050535073,0.00038900255,0.000015529022,0.00037777564],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.99993706,0.0000056261815,0.000009063754,0.000023669452,0.000011101227,0.000013501787],"domain_scores_gemma":[0.99990535,0.000016554472,0.00002752103,0.0000044421263,0.000013585363,0.000032559892],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00007701138,0.00040503131,0.00019904207,0.0005282092,0.00022189741,0.0002450403,0.00014590487,0.00036826808,0.001331521],"category_scores_gemma":[0.0002744031,0.000103069884,0.00016351147,0.0002910341,0.00015753793,0.0001757067,0.00025343217,0.00031577784,0.00039063962],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0006495116,0.000051604056,0.2072731,0.00018892079,0.00008368445,0.045217212,0.0007090925,0.0002612301,0.7208543,0.00021586443,0.000595783,0.023899714],"study_design_scores_gemma":[0.000024675823,0.00046578696,0.77471274,0.000049244998,0.00012461652,0.15253866,0.0005828379,0.0012889546,0.064679146,0.00026270622,0.0052439333,0.00002678681],"about_ca_topic_score_codex":0.0007648126,"about_ca_topic_score_gemma":0.0007651319,"teacher_disagreement_score":0.001331521,"about_ca_system_score_codex":0.00011344826,"about_ca_system_score_gemma":0.00009634088,"threshold_uncertainty_score":0.0044543147},"labels":[],"label_agreement":null},{"id":"W4411696543","doi":"10.1080/15592294.2025.2523191","title":"<i>PIK3R1</i> and <i>G0S2</i> are human placenta-specific imprinted genes associated with germline-inherited maternal DNA methylation","year":2025,"lang":"en","type":"article","venue":"Epigenetics","topic":"Genetic Syndromes and Imprinting","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":"University Hospital Foundation","funders":"Biotechnology and Biological Sciences Research Council; Fondation ARC pour la Recherche sur le Cancer; Medical Research Council; Ministerio de Economía y Competitividad; European Commission; Wellcome Trust","keywords":"Genomic imprinting; Biology; Imprinting (psychology); Differentially methylated regions; DNA methylation; Reprogramming; Epigenetics; Methylation; Genetics; Placenta; Germline; Gene; Gene expression; Fetus; Pregnancy","score_opus":0.010777392000606172,"score_gpt":0.24372743590884283,"score_spread":0.23295004390823665,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4411696543","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.963777,0.00652891,0.006384006,0.00018724272,0.00004248076,0.00005545885,0.01807581,0.0010139786,0.003934996],"genre_scores_gemma":[0.97975504,0.0016171901,0.00438242,0.0001490228,0.000010440756,0.000036269605,0.012105929,0.000098963574,0.0018448285],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99985886,0.000008906656,0.000008259886,0.000061805695,0.000036009365,0.000026146628],"domain_scores_gemma":[0.9998772,0.000021030077,0.00005744604,0.000012979604,0.000012905202,0.000018474217],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00011740667,0.00027388718,0.0003335054,0.0003585754,0.00020320828,0.0003840262,0.0001798067,0.00018691439,0.0017578715],"category_scores_gemma":[0.00032087287,0.00016402303,0.00032932562,0.00065835885,0.00023113083,0.00011927263,0.00029231858,0.00028025985,0.0006386647],"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":[0.00092220114,0.000016768916,0.049105022,0.00044663282,0.00020628194,0.00045684958,0.00016057702,0.00069086737,0.91339564,0.00052781333,0.0018821371,0.032189276],"study_design_scores_gemma":[0.00006482537,0.00020963006,0.62330306,0.00006357214,0.00033915357,0.003006652,0.00015767587,0.0035468447,0.34300783,0.0009910022,0.02525238,0.00005741555],"about_ca_topic_score_codex":0.0033963202,"about_ca_topic_score_gemma":0.0045543667,"teacher_disagreement_score":0.0033963202,"about_ca_system_score_codex":0.00034045303,"about_ca_system_score_gemma":0.00028993798,"threshold_uncertainty_score":0.0067531466},"labels":[],"label_agreement":null},{"id":"W4412430336","doi":"10.1172/jci168962","title":"Organ-specific features of human kidney lymphatics are disrupted in chronic transplant rejection","year":2025,"lang":"en","type":"article","venue":"Journal of Clinical Investigation","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":10,"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 Infection and Immunity","funders":"Foulkes Foundation; Rosetrees Trust; Kidney Research UK; National Institute for Health and Care Research; Wellcome Trust","keywords":"Lymphatic system; Kidney; Kidney transplantation; Pathology; Medicine; Organ transplantation; Graft rejection; Transplant rejection; Immunology; Transplantation; Biology; Immune system; Internal medicine","score_opus":0.03431954953857322,"score_gpt":0.3447410962103921,"score_spread":0.31042154667181887,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4412430336","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9974215,0.00054415176,0.0013790239,0.000024335031,0.0000032789223,0.0000055463493,0.00010702105,0.000028186465,0.00048694646],"genre_scores_gemma":[0.9989668,0.00025347222,0.00033919222,0.000010065082,0.0000026134949,0.00000406206,0.00010786334,0.0000055894307,0.0003103324],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.99990034,0.000018722425,0.000008659552,0.000025571102,0.000025424135,0.000021287235],"domain_scores_gemma":[0.99987936,0.000013941749,0.00006309263,0.000013781281,0.000007529406,0.000022315044],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00016135121,0.00013102018,0.00013964846,0.00030685536,0.00010325974,0.0002813479,0.00009361074,0.00014266252,0.0011063298],"category_scores_gemma":[0.0001874089,0.000078747566,0.00010107189,0.00022629602,0.00024810657,0.00014593254,0.0002613191,0.00018446434,0.00014771053],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0006797146,0.000027771535,0.03176041,0.00006837732,0.000022051545,0.0013977917,0.00014877689,0.00016856927,0.9552265,0.00047550414,0.000072118295,0.009952495],"study_design_scores_gemma":[0.000036269746,0.0004756993,0.58663917,0.000018329114,0.000099482895,0.023309119,0.00049739005,0.0011523425,0.3806416,0.0009516323,0.0061574066,0.000021688638],"about_ca_topic_score_codex":0.00021334618,"about_ca_topic_score_gemma":0.00019185121,"teacher_disagreement_score":0.0011063298,"about_ca_system_score_codex":0.00010928243,"about_ca_system_score_gemma":0.0001473473,"threshold_uncertainty_score":0.0037010312},"labels":[],"label_agreement":null},{"id":"W4412647599","doi":"10.1186/s13072-025-00612-7","title":"Identification of genetic and non-genetic modifiers of genomic imprinting through screening of imprinted DMR methylation in humans","year":2025,"lang":"en","type":"article","venue":"Epigenetics & Chromatin","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":2,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"London Health Sciences Centre; Western University","funders":"Associazione Italiana per la Ricerca sul Cancro; Fondazione Telethon; Government of Canada; Ministero dell’Istruzione, dell’Università e della Ricerca; Genome Canada; Ontario Genomics; Ontario Genomics Institute","keywords":"Genomic imprinting; Biology; Imprinting (psychology); Genetics; Identification (biology); Human genetics; Methylation; DNA methylation; Computational biology; Evolutionary biology; Gene; Gene expression; Ecology","score_opus":0.009737937297583843,"score_gpt":0.26503081419409186,"score_spread":0.25529287689650804,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4412647599","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.983313,0.0014705891,0.0105510475,0.000053226,0.0000063983216,0.000025478197,0.0034637246,0.000118727294,0.0009976431],"genre_scores_gemma":[0.98916596,0.0006456966,0.0074238675,0.000060613773,0.000008430638,0.00002613974,0.0021506385,0.000031754753,0.0004870022],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9998124,0.000029816885,0.000010040811,0.00010683449,0.0000263642,0.000014600573],"domain_scores_gemma":[0.9998492,0.000049419417,0.000039087867,0.000035149118,0.000011861385,0.000015207793],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00024168724,0.00017215018,0.00026014601,0.00058744836,0.00013716839,0.00023879431,0.00018196953,0.00017455632,0.0014719736],"category_scores_gemma":[0.00044729133,0.00013156892,0.00021535395,0.00050400797,0.00018160277,0.00008936664,0.00027516106,0.0001684024,0.00020549676],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00076799176,0.000055259297,0.32583117,0.00035444266,0.0006474724,0.0008402216,0.00056698546,0.0011858656,0.58481574,0.0005633205,0.00089938083,0.08347218],"study_design_scores_gemma":[0.000029287323,0.00025099594,0.9158328,0.00003695798,0.00024260127,0.003122541,0.00011667277,0.0026946173,0.070942685,0.00089957647,0.0058063995,0.000024785171],"about_ca_topic_score_codex":0.0010449745,"about_ca_topic_score_gemma":0.0010489743,"teacher_disagreement_score":0.0014719736,"about_ca_system_score_codex":0.00012204209,"about_ca_system_score_gemma":0.00010522748,"threshold_uncertainty_score":0.0049242377},"labels":[],"label_agreement":null},{"id":"W4413043874","doi":"10.1016/j.jpag.2025.07.011","title":"Sex Hormone Replacement Therapy and Bleeding Patterns among Adolescents and Young Adult Females with Prader–Willi Syndrome","year":2025,"lang":"en","type":"article","venue":"Journal of Pediatric and Adolescent Gynecology","topic":"Genetic Syndromes and Imprinting","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","funders":"","keywords":"Medicine; Discontinuation; Hypogonadotropic hypogonadism; Pediatrics; Cohort; Retrospective cohort study; Hormone replacement therapy (female-to-male); Young adult; Amenorrhea; Medical record; Gynecology; Internal medicine; Hormone; Testosterone (patch); Pregnancy","score_opus":0.00877229070462568,"score_gpt":0.22905813423431554,"score_spread":0.22028584352968986,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4413043874","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99958557,0.00010220278,0.000013220391,0.000019110197,0.000001805815,0.0000018867455,0.00006124864,8.2224665e-7,0.00021412481],"genre_scores_gemma":[0.9996117,0.00009868281,0.000022855238,0.00001966256,0.000004593045,0.000002302166,0.000089105575,7.290132e-7,0.00015031267],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9998505,0.00003529723,0.000023347095,0.000025759613,0.000033601737,0.000031487678],"domain_scores_gemma":[0.9995721,0.00010050184,0.00017251051,0.00001437709,0.000029489973,0.00011106931],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0001415665,0.00015506885,0.00027632172,0.00077550113,0.00027904034,0.0003407625,0.00013047163,0.00030104627,0.0012674327],"category_scores_gemma":[0.00094181934,0.00018199816,0.00025170005,0.0006546065,0.00018559098,0.00027027784,0.00020303864,0.00040936877,0.00014842705],"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":[0.000067774214,0.0000393,0.99837273,0.000002391089,0.000015692745,0.0003283029,0.00009464913,0.000009732231,0.00027928763,0.000009926036,0.000023763345,0.0007564521],"study_design_scores_gemma":[0.0000029566054,0.000085584325,0.99847,0.0000020804696,0.000011451067,0.00092380703,0.000338485,0.000044164113,0.00003896135,0.000007702369,0.00007290652,0.0000018774946],"about_ca_topic_score_codex":0.003891276,"about_ca_topic_score_gemma":0.0041668024,"teacher_disagreement_score":0.003891276,"about_ca_system_score_codex":0.00014815669,"about_ca_system_score_gemma":0.00014753596,"threshold_uncertainty_score":0.007737279},"labels":[],"label_agreement":null},{"id":"W4413051636","doi":"10.1177/19160216251364759","title":"Outcomes After Tonsillectomy in Children With Angelman Syndrome","year":2025,"lang":"en","type":"article","venue":"Journal of Otolaryngology - Head and Neck Surgery","topic":"Genetic Syndromes and Imprinting","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":"SickKids Foundation; University of Toronto; Children's Hospital of Eastern Ontario; University of Ottawa; Hospital for Sick Children","funders":"","keywords":"Angelman syndrome; Tonsillectomy; Medicine; Pediatrics; Psychology; Audiology; Surgery; Genetics; Biology","score_opus":0.006749925338824258,"score_gpt":0.23728858320458346,"score_spread":0.2305386578657592,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4413051636","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99569714,0.003161465,0.00007546152,0.00012228805,0.000018312334,0.000011483141,0.0004014203,0.0000061982,0.00050619897],"genre_scores_gemma":[0.99764204,0.0016272673,0.00011205957,0.00003290451,0.000016321414,0.000012162716,0.0004896368,0.0000034734653,0.00006427293],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9994486,0.000088139124,0.000101714104,0.00006353498,0.00017937408,0.00011858052],"domain_scores_gemma":[0.99718165,0.0005345008,0.0016959176,0.000050634168,0.00015745453,0.000379782],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0004626477,0.00024460192,0.00030136676,0.00084425695,0.00045386984,0.00049408985,0.00028483412,0.00025335414,0.0014159597],"category_scores_gemma":[0.003494947,0.00012528936,0.0005100286,0.0009824549,0.0004538043,0.00050356134,0.00045295185,0.00047551127,0.00010741203],"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":[0.000047934314,0.000011204512,0.99435586,0.00006471969,0.000035652654,0.0018639724,0.00016284453,0.000034884768,0.00013399748,0.000038425354,0.00019079822,0.0030595337],"study_design_scores_gemma":[0.000006811587,0.00015672689,0.9831403,0.00009830463,0.00004442141,0.014946885,0.00089466595,0.000084301195,0.00015848347,0.000041191328,0.00042019397,0.000007796076],"about_ca_topic_score_codex":0.0033800546,"about_ca_topic_score_gemma":0.005566403,"teacher_disagreement_score":0.0033800546,"about_ca_system_score_codex":0.0006139843,"about_ca_system_score_gemma":0.0006890088,"threshold_uncertainty_score":0.0067207813},"labels":[],"label_agreement":null},{"id":"W4413470125","doi":"10.1101/2025.08.19.670946","title":"PHLDA2 promotes breast cancer metastasis by co-opting a developmental program for placental vascular remodeling","year":2025,"lang":"en","type":"preprint","venue":"bioRxiv (Cold Spring Harbor Laboratory)","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":0,"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":"Canadian Institutes of Health Research; Mark Foundation For Cancer Research; Alexander von Humboldt-Stiftung; California Institute for Regenerative Medicine","keywords":"Metastasis; Breast cancer; Extracellular matrix; Cancer research; Cancer; Biology; Downregulation and upregulation; Ectopic expression; Medicine; Internal medicine; Cell biology; Gene; Genetics","score_opus":0.01170163615709603,"score_gpt":0.25379344334756443,"score_spread":0.2420918071904684,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4413470125","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9694234,0.0025114836,0.015710387,0.0007874608,0.00010547524,0.000027274144,0.0021704838,0.00080434675,0.0084595205],"genre_scores_gemma":[0.98958313,0.0006203765,0.0029148243,0.000073039955,0.000018854056,0.000020047848,0.0008763696,0.000101835256,0.0057915323],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9999293,0.000009042092,0.0000031762802,0.000019228175,0.000025205392,0.000013993705],"domain_scores_gemma":[0.9999442,0.000009341945,0.000013192685,0.000008475661,0.000005735077,0.000019073275],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00010598852,0.00015043409,0.000106035724,0.00022922546,0.00016951805,0.00030654308,0.000092093775,0.00016358803,0.0034173245],"category_scores_gemma":[0.00012319894,0.0001248125,0.00013666914,0.00015495931,0.0001800002,0.00011416178,0.0002844512,0.0004021872,0.00056788913],"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":[0.00009979094,0.000007962414,0.0017702068,0.000028921997,0.0000063662505,0.00016625582,0.000011749765,0.00015909148,0.9943585,0.00043655446,0.0004559393,0.0024986437],"study_design_scores_gemma":[0.000028413566,0.000058001708,0.0273237,0.000007736519,0.000016694763,0.0012778522,0.00004233185,0.0026990557,0.9507516,0.0004938277,0.017294494,0.0000062038707],"about_ca_topic_score_codex":0.0006848416,"about_ca_topic_score_gemma":0.0010725117,"teacher_disagreement_score":0.0034173245,"about_ca_system_score_codex":0.0002950432,"about_ca_system_score_gemma":0.00018115932,"threshold_uncertainty_score":0.011432052},"labels":[],"label_agreement":null},{"id":"W4413865128","doi":"10.1080/23772484.2025.2551371","title":"Tongue reduction surgery in Beckwith-Wiedemann syndrome, effects on eating and swallowing function: A case report","year":2025,"lang":"en","type":"article","venue":"Acta Oto-Laryngologica Case Reports","topic":"Genetic Syndromes and Imprinting","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":"Children's & Women's Health Centre of British Columbia","funders":"","keywords":"Beckwith–Wiedemann syndrome; Swallowing; Medicine; Tongue; Reduction (mathematics); Surgery; Biology; Pathology; Mathematics; Genetics","score_opus":0.009042725035187077,"score_gpt":0.2413880340848116,"score_spread":0.23234530904962453,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4413865128","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99373734,0.002092671,0.0006867754,0.0006090996,0.000074690135,0.00004705888,0.00007454006,0.000048895523,0.002628951],"genre_scores_gemma":[0.9967618,0.0011312392,0.00075536116,0.00017016784,0.0001346512,0.000015739655,0.000042159038,0.000011357496,0.0009774405],"study_design_codex":"case_report","study_design_gemma":"case_report","domain_scores_codex":[0.99960595,0.00003827897,0.000049464725,0.000084636406,0.0000756929,0.00014605933],"domain_scores_gemma":[0.99925286,0.00020586899,0.00025582453,0.00004072497,0.00003532589,0.0002092897],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00017583727,0.0015122585,0.00070192956,0.0017721184,0.0022118303,0.00097976,0.0007899183,0.0028089923,0.0018360828],"category_scores_gemma":[0.0015471604,0.0008503177,0.0007655275,0.0008886983,0.0018273698,0.00094230176,0.0012767202,0.0016314493,0.00035324608],"study_design_candidate":"case_report","study_design_consensus":"case_report","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.000008958841,0.000010892999,0.004231712,0.000011053033,0.000003890929,0.99462897,0.000108552245,0.000014689745,0.0004366195,0.000041489864,0.0000419869,0.00046116844],"study_design_scores_gemma":[0.000002523402,0.000030245948,0.003680263,0.0000051018815,0.00000816961,0.9957743,0.000113533824,0.00003349029,0.00021340566,0.000026128697,0.000108792774,0.000004014979],"about_ca_topic_score_codex":0.004145348,"about_ca_topic_score_gemma":0.0061101024,"teacher_disagreement_score":0.004145348,"about_ca_system_score_codex":0.0009222848,"about_ca_system_score_gemma":0.00083391025,"threshold_uncertainty_score":0.008242428},"labels":[],"label_agreement":null},{"id":"W4414189985","doi":"10.7759/cureus.92316","title":"Peripheral Precocious Puberty Due to Autonomous Gonadal Activation: A Multicenter Experience","year":2025,"lang":"en","type":"article","venue":"Cureus","topic":"Genetic Syndromes and Imprinting","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":"Child, Adolescent and Family Mental Health","funders":"","keywords":"Precocious puberty; Peripheral; Intervention (counseling); Delayed puberty","score_opus":0.008811375058414252,"score_gpt":0.2654567955905583,"score_spread":0.25664542053214406,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4414189985","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99908173,0.00022923465,0.000100126395,0.000023710247,0.00000398989,0.00003952275,0.00006658377,0.00000421874,0.0004508239],"genre_scores_gemma":[0.9991425,0.0003127012,0.00023776531,0.000038536753,0.000020021378,0.000028903269,0.00012068507,0.0000042219867,0.000094637675],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9991622,0.00028587529,0.00011853037,0.00016332218,0.00011274106,0.00015731291],"domain_scores_gemma":[0.99867994,0.00029792247,0.00039651326,0.00015364059,0.0001328879,0.000339093],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00097571296,0.00044966358,0.0004017502,0.0007163477,0.0007461787,0.00072511216,0.0004669927,0.0003712465,0.0019007201],"category_scores_gemma":[0.001977215,0.00030007746,0.0003132946,0.0011777455,0.00063035754,0.00053673174,0.0010284622,0.00043501597,0.00041369413],"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":[0.00025672722,0.00052775914,0.9698608,0.00007890763,0.00003828149,0.015833462,0.0023698097,0.00005611142,0.001145154,0.000062001796,0.00026954222,0.009501598],"study_design_scores_gemma":[0.00014181857,0.003964436,0.8853977,0.00009041588,0.00006978787,0.10046384,0.007039217,0.0002180161,0.0007175527,0.00005855469,0.0018047688,0.00003404012],"about_ca_topic_score_codex":0.0020729098,"about_ca_topic_score_gemma":0.0023487469,"teacher_disagreement_score":0.0020729098,"about_ca_system_score_codex":0.0004550597,"about_ca_system_score_gemma":0.00071590993,"threshold_uncertainty_score":0.006358564},"labels":[],"label_agreement":null},{"id":"W4414526620","doi":"10.1210/jcemcr/luaf221","title":"Late Diagnosis of Prader-Willi Syndrome in an Adolescent With Significant Complications of Type 2 Diabetes","year":2025,"lang":"en","type":"article","venue":"JCEM Case Reports","topic":"Genetic Syndromes and Imprinting","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":"Hospital for Sick Children","funders":"","keywords":"Type 2 diabetes; Glycated hemoglobin; Diabetes mellitus; Socioeconomic status; Nephrotic syndrome; Type 1 diabetes","score_opus":0.013891197457164158,"score_gpt":0.2597249773187525,"score_spread":0.24583377986158833,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4414526620","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9896465,0.0016040407,0.0018382245,0.0026602943,0.00022311512,0.000099298355,0.00013598932,0.000055634537,0.0037370096],"genre_scores_gemma":[0.996807,0.0008735035,0.0010177251,0.00045761897,0.00029187236,0.000019205736,0.000054212607,0.0000107792375,0.00046813433],"study_design_codex":"case_report","study_design_gemma":"case_report","domain_scores_codex":[0.9995426,0.000065708184,0.00004964675,0.00011577933,0.000084675274,0.00014155121],"domain_scores_gemma":[0.9987808,0.00033512086,0.00028988728,0.000037576556,0.00006998774,0.0004866352],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00033226167,0.0011059574,0.0007008984,0.0016147023,0.0017143616,0.000915192,0.0008116014,0.0023093917,0.0012754386],"category_scores_gemma":[0.0028399457,0.00057370495,0.0005461117,0.0007749729,0.00097427174,0.0011438298,0.0010377335,0.0026187245,0.00023603],"study_design_candidate":"case_report","study_design_consensus":"case_report","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.000014760429,0.000037449718,0.02173429,0.000013702672,0.0000049149394,0.9762774,0.00020202983,0.000052605217,0.00032754143,0.00018746908,0.00018605916,0.0009616384],"study_design_scores_gemma":[0.0000053312915,0.000053515887,0.010835924,0.00002174139,0.000007730766,0.98808694,0.00017016755,0.00019376542,0.00016961958,0.00011893054,0.0003287569,0.0000076197716],"about_ca_topic_score_codex":0.0029228593,"about_ca_topic_score_gemma":0.0051493854,"teacher_disagreement_score":0.0029228593,"about_ca_system_score_codex":0.00081593916,"about_ca_system_score_gemma":0.0009261642,"threshold_uncertainty_score":0.005920112},"labels":[],"label_agreement":null},{"id":"W4414830981","doi":"10.1093/jas/skaf300.473","title":"PSVI-11 Role of differentially expressed and imprinted genes in high and low fertility produced cattle pregnancies.","year":2025,"lang":"en","type":"article","venue":"Journal of Animal Science","topic":"Genetic Syndromes and Imprinting","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":"University of British Columbia","funders":"","keywords":"Conceptus; Genomic imprinting; Sire; Gene; Transcriptome; Embryo; Candidate gene; Estrous cycle","score_opus":0.0061400961333712934,"score_gpt":0.23700934132095217,"score_spread":0.23086924518758087,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4414830981","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9958974,0.0009850407,0.0006653307,0.000025575242,0.000010624716,0.0000044123494,0.0018167294,0.000020611758,0.0005743969],"genre_scores_gemma":[0.9946445,0.00026893456,0.0010874756,0.00003231568,0.00000559365,0.000011170461,0.002472028,0.000014182921,0.0014637988],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.99985707,0.000017882103,0.0000056870103,0.00005358395,0.00003116488,0.000034636145],"domain_scores_gemma":[0.9998609,0.00003808385,0.00004920907,0.0000056848094,0.000011917809,0.00003423798],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00019497146,0.00015482122,0.00021716807,0.00039805763,0.00018890404,0.0004262926,0.000105330386,0.00015353985,0.0010507611],"category_scores_gemma":[0.00016985652,0.0001010164,0.00018788804,0.00037383055,0.00016365529,0.00009029675,0.00017708405,0.0002741649,0.00018554427],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0008576475,0.00003621727,0.07555412,0.0001146164,0.000054024385,0.00016517547,0.00017559479,0.00021144887,0.9152094,0.00013374939,0.00018505832,0.00730295],"study_design_scores_gemma":[0.000008094048,0.00027231826,0.9453888,0.000015152247,0.000064961416,0.0004309418,0.00017937996,0.0012058591,0.050662175,0.00008766309,0.0016770819,0.000007505129],"about_ca_topic_score_codex":0.0010395774,"about_ca_topic_score_gemma":0.0014356184,"teacher_disagreement_score":0.0010507611,"about_ca_system_score_codex":0.00019749718,"about_ca_system_score_gemma":0.0001367823,"threshold_uncertainty_score":0.003515184},"labels":[],"label_agreement":null},{"id":"W4415352898","doi":"10.1101/2025.10.19.25338239","title":"Geography, Ancestry, Age and Sex Shape Somatic Autosomal Mosaic Chromosomal Alterations in Blood","year":2025,"lang":"en","type":"preprint","venue":"medRxiv","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":0,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":true,"ca_institutions":"Concordia University; Wilfrid Laurier University; Vector Institute; Ontario Institute for Cancer Research; Amgen (Canada); University of Toronto","funders":"National Institute of Environmental Health Sciences; National Human Genome Research Institute; National Cancer Institute; National Institutes of Health; Partenariat Canadien Contre Le Cancer; Health Canada; Government of Ontario","keywords":"Germline; Germline mutation; Somatic cell; Heritability; Genetic variation; Mosaic; Population; Missing heritability problem","score_opus":0.015384877325018871,"score_gpt":0.26030946620960743,"score_spread":0.24492458888458857,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4415352898","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9964551,0.00034036642,0.0009285798,0.000086593805,0.0000041987973,0.0000037505918,0.00088379777,0.00002793533,0.0012698786],"genre_scores_gemma":[0.9985435,0.00017890461,0.00041998565,0.000027085389,0.0000024394383,0.0000019534666,0.00025900785,0.000015950003,0.0005512818],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9998111,0.00003799845,0.00000676623,0.000067488974,0.00004020055,0.0000364141],"domain_scores_gemma":[0.9998215,0.000045045967,0.000060186143,0.000022952594,0.000020629705,0.000029712044],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00027542692,0.00017694767,0.0001742799,0.000491874,0.00030950052,0.0005023398,0.00016276311,0.00016853846,0.002405408],"category_scores_gemma":[0.00081209844,0.000086994325,0.00018267272,0.00059681525,0.0003903686,0.00011882547,0.0002929223,0.00016218571,0.00018372326],"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":[0.00026397145,0.000010311881,0.9066772,0.000043697557,0.00018611611,0.0006966212,0.00086221506,0.0014357553,0.056817453,0.0011821785,0.0009269734,0.030897686],"study_design_scores_gemma":[0.0000036928527,0.000014004683,0.99532384,0.000007346321,0.000033529777,0.00036341065,0.0002122023,0.0007260713,0.0019849716,0.00035433302,0.0009694588,0.0000072335442],"about_ca_topic_score_codex":0.073324986,"about_ca_topic_score_gemma":0.12938602,"teacher_disagreement_score":0.073324986,"about_ca_system_score_codex":0.0005091706,"about_ca_system_score_gemma":0.0004492371,"threshold_uncertainty_score":0.14579636},"labels":[],"label_agreement":null},{"id":"W4415388695","doi":"10.1111/jir.70053","title":"Codesigning a Neurocognitive Assessment Protocol for Hyperphagia: Perspectives From Stakeholders in Prader–Willi Syndrome","year":2025,"lang":"en","type":"article","venue":"Journal of Intellectual Disability Research","topic":"Genetic Syndromes and Imprinting","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":"University of Toronto; Centre for Addiction and Mental Health; SickKids Foundation; Hospital for Sick Children; Mental Health Research Canada","funders":"","keywords":"Neurocognitive; Protocol (science); Cognition; Stakeholder; Clinical trial; MEDLINE","score_opus":0.16058149419635448,"score_gpt":0.45914981158828366,"score_spread":0.2985683173919292,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4415388695","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.66546637,0.000863968,0.22153044,0.041654322,0.0011345636,0.05373081,0.0006419271,0.0012221164,0.0137554305],"genre_scores_gemma":[0.6191814,0.0006843278,0.2956435,0.008410837,0.0002415527,0.072505705,0.0004083188,0.00029390305,0.0026304014],"study_design_codex":"design_other","study_design_gemma":"qualitative","domain_scores_codex":[0.8479797,0.1319961,0.0074545704,0.0026109088,0.006937859,0.0030208435],"domain_scores_gemma":[0.8040343,0.12792963,0.011514666,0.01364802,0.035197277,0.007676187],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.17082061,0.00069469365,0.0005552804,0.0011648828,0.0034399668,0.0028877927,0.0030175592,0.0034968124,0.002059309],"category_scores_gemma":[0.2599225,0.00046922918,0.0009178122,0.00079480803,0.0027992614,0.0034139613,0.0066486793,0.004397987,0.00072795333],"study_design_candidate":"qualitative","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0024345797,0.004980594,0.035090216,0.0039853817,0.00010272951,0.0038208906,0.2903102,0.003197533,0.019185241,0.0063651516,0.027667092,0.6028604],"study_design_scores_gemma":[0.0030572969,0.014581216,0.12371807,0.017236767,0.00040473414,0.008459094,0.33682585,0.038089473,0.053052615,0.03709743,0.36550757,0.0019698406],"about_ca_topic_score_codex":0.003493589,"about_ca_topic_score_gemma":0.0065826117,"teacher_disagreement_score":0.17082061,"about_ca_system_score_codex":0.006590499,"about_ca_system_score_gemma":0.017425878,"threshold_uncertainty_score":0.90339655},"labels":[],"label_agreement":null},{"id":"W4415450113","doi":"10.1210/jendso/bvaf149.1774","title":"SAT-206 Development of a Minimum Dataset (MDS) for the Monitoring of Growth Hormone Therapy in Children with Prader Willi Syndrome (PWS) - A GloBE-Reg Initiative","year":2025,"lang":"en","type":"article","venue":"Journal of the Endocrine Society","topic":"Genetic Syndromes and Imprinting","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":"Trinity College","funders":"","keywords":"Consistency (knowledge bases); Data collection; Growth hormone; Human growth hormone; Clinical trial; Quality (philosophy); Data quality","score_opus":0.013573048782031773,"score_gpt":0.26830445786840357,"score_spread":0.2547314090863718,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4415450113","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":[0.047221307,0.00063077285,0.019743582,0.0025582265,0.00030037182,0.0034590182,0.91726446,0.0043775407,0.0044447337],"genre_scores_gemma":[0.02639413,0.000122606,0.026296772,0.00036265724,0.000044897453,0.0036935846,0.94224834,0.00018274302,0.0006543025],"study_design_codex":"not_applicable","study_design_gemma":"theoretical_or_conceptual","domain_scores_codex":[0.9902711,0.004397239,0.0018495007,0.0013802656,0.0017060398,0.00039584798],"domain_scores_gemma":[0.9701526,0.0101063335,0.0038473145,0.00491828,0.008506641,0.002468806],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.018921318,0.0010450279,0.0013403505,0.0030127557,0.000818502,0.0020277316,0.0036687145,0.0018444116,0.0064396006],"category_scores_gemma":[0.04928773,0.0005539931,0.0027924879,0.0025158082,0.0004052729,0.0014839097,0.004002144,0.0017219761,0.004360846],"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":[0.0065948046,0.0010253679,0.20246658,0.005137,0.0020974043,0.0004980081,0.00067389064,0.01195735,0.004952306,0.0046970374,0.6265385,0.13336164],"study_design_scores_gemma":[0.0069279764,0.002703673,0.3766788,0.0032989976,0.0012983534,0.0009360821,0.0010916177,0.07853132,0.010168477,0.0064516715,0.511561,0.00035201653],"about_ca_topic_score_codex":0.013060442,"about_ca_topic_score_gemma":0.016468368,"teacher_disagreement_score":0.018921318,"about_ca_system_score_codex":0.0020001773,"about_ca_system_score_gemma":0.007671466,"threshold_uncertainty_score":0.10006666},"labels":[],"label_agreement":null},{"id":"W4415988284","doi":"10.4244/eij-e-25-00046","title":"HALT &amp;ndash; an evolving understanding of the mechanisms of formation and clinical relevance","year":2025,"lang":"en","type":"article","venue":"EuroIntervention","topic":"Genetic Syndromes and Imprinting","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":"St. Paul's Hospital; University of British Columbia","funders":"","keywords":"Clinical significance; Relevance (law); MEDLINE; Mechanism (biology)","score_opus":0.04608982617497265,"score_gpt":0.32808199130562643,"score_spread":0.2819921651306538,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4415988284","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":[0.03303542,0.66468024,0.04390011,0.1210789,0.008884585,0.00014962321,0.0007207156,0.0012467002,0.1263037],"genre_scores_gemma":[0.38659734,0.4182722,0.047377348,0.0293275,0.015559558,0.00032009307,0.0007411011,0.0005974078,0.10120752],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.9995431,0.000101653895,0.000042881828,0.00010249076,0.00016820196,0.000041683918],"domain_scores_gemma":[0.9980165,0.0011851923,0.00026321548,0.000103313745,0.00020580496,0.00022606831],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0012372407,0.0005163919,0.0007071391,0.00089744537,0.0005422064,0.0023210812,0.0011005863,0.0025024512,0.014336922],"category_scores_gemma":[0.0029564337,0.0002159169,0.0002826365,0.00052308297,0.002566962,0.001306223,0.0010548729,0.0033560232,0.0037987626],"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":[0.0007782436,0.00014068442,0.0072980663,0.0019267069,0.00010144984,0.008526297,0.0002456073,0.0010944646,0.013284942,0.066788055,0.05378786,0.8460277],"study_design_scores_gemma":[0.00024353819,0.0006571412,0.01538713,0.0018098282,0.00012903895,0.043938372,0.000556821,0.0044887713,0.029791296,0.079338215,0.8235033,0.00015656059],"about_ca_topic_score_codex":0.0011789865,"about_ca_topic_score_gemma":0.0016219429,"teacher_disagreement_score":0.014336922,"about_ca_system_score_codex":0.0014923583,"about_ca_system_score_gemma":0.001481637,"threshold_uncertainty_score":0.04796177},"labels":[],"label_agreement":null},{"id":"W4416343701","doi":"10.1016/j.placenta.2025.08.110","title":"Loss of maternally imprinted Sfmbt2 microRNA cluster results in placental junctional zone abnormalities and FGR in mice","year":2025,"lang":"en","type":"article","venue":"Placenta","topic":"Genetic Syndromes and Imprinting","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":"Lunenfeld-Tanenbaum Research Institute; University of Toronto; Mount Sinai Hospital","funders":"","keywords":"microRNA; Genomic imprinting; Cluster (spacecraft); Placenta","score_opus":0.005163278851479605,"score_gpt":0.22752422390185265,"score_spread":0.22236094505037304,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4416343701","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.97321385,0.0018310496,0.01475769,0.00066351454,0.00019840687,0.00008893772,0.004169563,0.0015844713,0.003492567],"genre_scores_gemma":[0.9780864,0.0010673578,0.007560271,0.00023832127,0.00006405948,0.00014875298,0.001465146,0.00082514936,0.01054457],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9989697,0.00013905659,0.00012580868,0.0003110963,0.0003009414,0.0001534371],"domain_scores_gemma":[0.99876237,0.00020263054,0.00058416644,0.00010913078,0.000029946323,0.00031172606],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0004223468,0.0012720858,0.0006996849,0.0028256853,0.0006289851,0.0009795098,0.0009923583,0.0017611888,0.006744143],"category_scores_gemma":[0.0004480144,0.0010522201,0.0010631634,0.00074950606,0.0016603747,0.0004693665,0.00089365034,0.0020303754,0.0012008516],"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":[0.00040332988,0.0000575652,0.00035494077,0.000047591973,0.00003227834,0.0010377975,0.00005335678,0.0002363996,0.99580896,0.00076055597,0.00013614233,0.0010710702],"study_design_scores_gemma":[0.00019806028,0.00028451896,0.007452414,0.000030477986,0.00015324923,0.0043249433,0.00014775098,0.002507962,0.97927547,0.0004371188,0.0051520416,0.000035969464],"about_ca_topic_score_codex":0.0018841262,"about_ca_topic_score_gemma":0.0027584317,"teacher_disagreement_score":0.006744143,"about_ca_system_score_codex":0.0007186849,"about_ca_system_score_gemma":0.00055117736,"threshold_uncertainty_score":0.02256143},"labels":[],"label_agreement":null},{"id":"W4416902275","doi":"10.1111/cpr.70150","title":"Analysis of Human Uniparental Embryonic Stem Cells Reveals New Putative Imprinted Loci","year":2025,"lang":"en","type":"article","venue":"Cell Proliferation","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":0,"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":"HORIZON EUROPE Health; Azrieli Foundation; Israel Science Foundation; United States-Israel Binational Science Foundation; HORIZON EUROPE Framework Programme; Rosetrees Trust; European Commission","keywords":"Genomic imprinting; Epigenetics; Imprinting (psychology); Embryonic stem cell; DNA methylation; Induced pluripotent stem cell; Gene; Transcriptome","score_opus":0.011090431045441662,"score_gpt":0.26579381092282833,"score_spread":0.25470337987738667,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4416902275","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9862006,0.001931628,0.0093804095,0.000049059283,0.000011088566,0.000028617746,0.0014261295,0.00005722678,0.0009154133],"genre_scores_gemma":[0.98568416,0.0012444899,0.009003697,0.00004395414,0.0000070673077,0.000021393485,0.0027101152,0.000016702945,0.0012684447],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.999928,0.000008342729,0.00000668103,0.000021626729,0.000026409376,0.000008928039],"domain_scores_gemma":[0.99992085,0.000025791096,0.000022261722,0.000009950847,0.00000823562,0.000012882131],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00008739484,0.00017078075,0.00011502745,0.00032617757,0.000096075564,0.00014693874,0.00015023569,0.00008199943,0.00065926864],"category_scores_gemma":[0.00016184783,0.0000801664,0.00013110903,0.00022827956,0.0001290006,0.000059022568,0.00015192869,0.0001602161,0.00021156821],"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":[0.000059269205,0.0000042169454,0.002383926,0.00002811851,0.000011253342,0.000086172964,0.000019014235,0.000055599572,0.9931994,0.00008307327,0.000015067629,0.0040547326],"study_design_scores_gemma":[0.000010435789,0.00022399133,0.1421334,0.000009209095,0.000071666735,0.0011889286,0.00005563268,0.0011575092,0.8500619,0.00025247532,0.0048270924,0.000007771679],"about_ca_topic_score_codex":0.00053066097,"about_ca_topic_score_gemma":0.0010546648,"teacher_disagreement_score":0.00065926864,"about_ca_system_score_codex":0.0001103435,"about_ca_system_score_gemma":0.00010126852,"threshold_uncertainty_score":0.0022054315},"labels":[],"label_agreement":null},{"id":"W6888996397","doi":"10.25384/sage.19307754","title":"sj-pdf-1-jcn-10.1177_08830738221081244 - Supplemental material for Further Characterization of <i>SMC1A</i> Loss of Function Epilepsy Distinct From Cornelia de Lange Syndrome","year":2022,"lang":"en","type":"article","venue":"Sage Journals Data","topic":"Genetic Syndromes and Imprinting","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 de Sherbrooke","funders":"","keywords":"Cornelia de Lange Syndrome; Epilepsy; Loss function; Neurology; Function (biology)","score_opus":0.020017718384738037,"score_gpt":0.2576234164026141,"score_spread":0.23760569801787607,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W6888996397","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":[0.017475158,0.00090294186,0.009502096,0.002396673,0.0016706289,0.00089710776,0.76042557,0.0034233981,0.20330648],"genre_scores_gemma":[0.026441054,0.00087171915,0.0078898845,0.00088392943,0.00022952651,0.0005373068,0.83687496,0.0030160036,0.12325557],"study_design_codex":"not_applicable","study_design_gemma":"not_applicable","domain_scores_codex":[0.9989009,0.00007790271,0.00012880441,0.00016189653,0.0005170107,0.00021336255],"domain_scores_gemma":[0.9977773,0.000621484,0.0001706394,0.00037869526,0.00037966797,0.0006722223],"candidate_categories":["insufficient_payload"],"consensus_categories":["insufficient_payload"],"category_scores_codex":[0.001071936,0.0008717643,0.0008443781,0.0034715596,0.0020150975,0.0017096538,0.002445789,0.0021641261,0.58528405],"category_scores_gemma":[0.0020727827,0.00095294317,0.0007648154,0.0033201315,0.0006090242,0.0015184792,0.0015491408,0.0029920521,0.30990225],"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":[0.0013495396,0.0009881194,0.0043735756,0.0008234493,0.00010191129,0.0013182932,0.00030779387,0.00038486088,0.27653083,0.008985316,0.6587015,0.04613482],"study_design_scores_gemma":[0.0003784632,0.00030024926,0.02837455,0.00024533598,0.00005074845,0.002031789,0.0002701598,0.0006152636,0.063543595,0.0018580476,0.9022379,0.00009389324],"about_ca_topic_score_codex":0.0068715736,"about_ca_topic_score_gemma":0.014443025,"teacher_disagreement_score":0.41471595,"about_ca_system_score_codex":0.0018615916,"about_ca_system_score_gemma":0.0014897437,"threshold_uncertainty_score":0.59154195},"labels":[],"label_agreement":null},{"id":"W6889108574","doi":"10.25384/sage.19307754.v1","title":"sj-pdf-1-jcn-10.1177_08830738221081244 - Supplemental material for Further Characterization of <i>SMC1A</i> Loss of Function Epilepsy Distinct From Cornelia de Lange Syndrome","year":2022,"lang":"en","type":"article","venue":"Figshare","topic":"Genetic Syndromes and Imprinting","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 de Sherbrooke","funders":"","keywords":"Cornelia de Lange Syndrome; Epilepsy; Loss function; Neurology; Function (biology)","score_opus":0.012900142201018398,"score_gpt":0.21949446814310822,"score_spread":0.20659432594208982,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W6889108574","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":[0.031223202,0.0019437901,0.019514343,0.0031451795,0.002432686,0.0014136729,0.67849064,0.004247987,0.25758842],"genre_scores_gemma":[0.052008394,0.0015835866,0.013627429,0.0010842546,0.00030535873,0.0007516582,0.77166635,0.003786244,0.15518671],"study_design_codex":"not_applicable","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99911326,0.00007118202,0.00010012153,0.00014047169,0.00038649852,0.0001883929],"domain_scores_gemma":[0.99860424,0.00039058522,0.0001195933,0.00023614526,0.00020130844,0.00044809462],"candidate_categories":["insufficient_payload"],"consensus_categories":[],"category_scores_codex":[0.0009606434,0.00091824605,0.00077492004,0.0029420294,0.002048623,0.0015420017,0.0023572843,0.0023674064,0.506087],"category_scores_gemma":[0.0016357369,0.00094067986,0.00080652465,0.0026027272,0.000602942,0.0014160817,0.0015159372,0.0030416343,0.24991292],"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":[0.0012911371,0.0009905989,0.0039132456,0.0008515006,0.000117189695,0.0020340546,0.00034666824,0.0004862439,0.4472622,0.012433764,0.48431483,0.04595863],"study_design_scores_gemma":[0.00034645366,0.00028080939,0.02614878,0.00024814782,0.00006016556,0.0031620867,0.00025848855,0.00079904567,0.08070566,0.0019905465,0.88590455,0.000095238014],"about_ca_topic_score_codex":0.0053554694,"about_ca_topic_score_gemma":0.0118832225,"teacher_disagreement_score":0.506087,"about_ca_system_score_codex":0.0018240276,"about_ca_system_score_gemma":0.0012663105,"threshold_uncertainty_score":0.70450693},"labels":[],"label_agreement":null},{"id":"W6901816567","doi":"10.6084/m9.figshare.20064365","title":"Additional file 7 of Gain and loss of TASK3 channel function and its regulation by novel variation cause KCNK9 imprinting syndrome","year":2022,"lang":"en","type":"article","venue":"Figshare","topic":"Genetic Syndromes and Imprinting","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":"BC Children's Hospital","funders":"","keywords":"Function (biology); Channel (broadcasting); HEK 293 cells; Gene; Loss function; Variation (astronomy); Cell","score_opus":0.013486072645029401,"score_gpt":0.20281614346042673,"score_spread":0.18933007081539732,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W6901816567","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":[0.00037369167,0.000028869194,0.00033643466,0.00010509678,0.000033315686,0.000058248563,0.99798834,0.00032997382,0.0007459955],"genre_scores_gemma":[0.018672619,0.00027139857,0.004277602,0.0008953407,0.00021606396,0.0012870474,0.96196365,0.0012664776,0.011149791],"study_design_codex":"not_applicable","study_design_gemma":"not_applicable","domain_scores_codex":[0.9992193,0.000102934624,0.00015913782,0.00019906327,0.00020368834,0.00011582502],"domain_scores_gemma":[0.9762324,0.018806824,0.0013612965,0.0012658656,0.0017580527,0.0005755633],"candidate_categories":["insufficient_payload"],"consensus_categories":["insufficient_payload"],"category_scores_codex":[0.0012486118,0.0011868507,0.00169775,0.0021222106,0.000935286,0.0014569847,0.0022395668,0.0015532692,0.87263536],"category_scores_gemma":[0.02447355,0.0006636521,0.0012301133,0.0028660886,0.00033115927,0.0014087403,0.00089142186,0.00093134044,0.14934719],"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":[0.0006842881,0.00016030158,0.005737908,0.0033344133,0.00012816962,0.00046716226,0.000098789365,0.0006289902,0.00058493466,0.00079360907,0.974683,0.012698477],"study_design_scores_gemma":[0.0146105895,0.0008418925,0.109180994,0.0063844887,0.00074609637,0.00479532,0.00071271026,0.003939361,0.0039248373,0.024533533,0.82988876,0.00044136844],"about_ca_topic_score_codex":0.00698639,"about_ca_topic_score_gemma":0.010836364,"teacher_disagreement_score":0.12736464,"about_ca_system_score_codex":0.0008663764,"about_ca_system_score_gemma":0.0012680171,"threshold_uncertainty_score":0.18167013},"labels":[],"label_agreement":null},{"id":"W6902075749","doi":"10.6084/m9.figshare.28040116","title":"Additional file 4 of Cognitive benefits of folic acid supplementation during pregnancy track with epigenetic changes at an imprint regulator","year":2024,"lang":"en","type":"article","venue":"Figshare","topic":"Genetic Syndromes and Imprinting","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":"University of British Columbia","funders":"","keywords":"Regulator; Track (disk drive); Epigenetics; Pregnancy; Folic acid; Folic acid supplementation","score_opus":0.0175098936779545,"score_gpt":0.24244197318072602,"score_spread":0.22493207950277153,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W6902075749","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":[0.00019489734,0.000026882584,0.00028461893,0.00009651661,0.000034223704,0.00007324636,0.9982343,0.00030342984,0.0007519256],"genre_scores_gemma":[0.009701387,0.0002514736,0.0055805296,0.0008164971,0.00014914316,0.0022906847,0.9665972,0.0012117215,0.013401269],"study_design_codex":"not_applicable","study_design_gemma":"not_applicable","domain_scores_codex":[0.9993886,0.00009428546,0.00009284681,0.00015822027,0.0001665837,0.00009958814],"domain_scores_gemma":[0.985482,0.011152625,0.0006955527,0.0007821408,0.0015384364,0.00034923555],"candidate_categories":["insufficient_payload"],"consensus_categories":[],"category_scores_codex":[0.0012465953,0.0013101965,0.0016510959,0.0016876109,0.0010529156,0.0016135874,0.0018116263,0.0014301288,0.9072376],"category_scores_gemma":[0.019210929,0.00063695415,0.0012745393,0.0025697374,0.00026362637,0.0013597899,0.00089163333,0.0009537752,0.17377222],"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":[0.0012465122,0.00021891779,0.0025554157,0.0048841108,0.00012205532,0.00015159944,0.000084247695,0.0005781629,0.0006021322,0.0007304828,0.97385186,0.014974468],"study_design_scores_gemma":[0.017349083,0.0011410626,0.06099871,0.00614681,0.0006300777,0.0012596333,0.0005680081,0.0028617845,0.003966995,0.016469369,0.88823736,0.00037108452],"about_ca_topic_score_codex":0.008704638,"about_ca_topic_score_gemma":0.013029305,"teacher_disagreement_score":0.9072376,"about_ca_system_score_codex":0.0011232054,"about_ca_system_score_gemma":0.0016340322,"threshold_uncertainty_score":0.13231432},"labels":[],"label_agreement":null},{"id":"W6902109544","doi":"10.6084/m9.figshare.20064371","title":"Additional file 9 of Gain and loss of TASK3 channel function and its regulation by novel variation cause KCNK9 imprinting syndrome","year":2022,"lang":"en","type":"article","venue":"Figshare","topic":"Genetic Syndromes and Imprinting","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":"BC Children's Hospital","funders":"","keywords":"Function (biology); Loss function; Channel (broadcasting); Gene; HEK 293 cells; Variation (astronomy); Mutation","score_opus":0.013477445620077237,"score_gpt":0.20279957040024266,"score_spread":0.1893221247801654,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W6902109544","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":[0.00029882145,0.000027870292,0.00021081616,0.00012496319,0.00003171788,0.0000546773,0.99824893,0.00021932663,0.00078284054],"genre_scores_gemma":[0.016723836,0.00028415787,0.0032018486,0.00096037093,0.00020370906,0.0012108405,0.9637433,0.00092594326,0.012745861],"study_design_codex":"not_applicable","study_design_gemma":"observational","domain_scores_codex":[0.9991873,0.00012086971,0.00016944147,0.0002118392,0.00019407578,0.000116439965],"domain_scores_gemma":[0.97819406,0.016888132,0.0014045394,0.001119869,0.0017852952,0.00060808985],"candidate_categories":["insufficient_payload"],"consensus_categories":[],"category_scores_codex":[0.0012432886,0.0010631512,0.001477053,0.0021385755,0.00093532074,0.0014674537,0.001859516,0.0014036702,0.870145],"category_scores_gemma":[0.027070213,0.0005703157,0.001134919,0.0029688287,0.00031243585,0.0014193058,0.0009370431,0.000852999,0.14028762],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0006430771,0.00012407788,0.0055787573,0.0029998424,0.00010661758,0.000341783,0.000095479,0.00044222537,0.00033888445,0.0007235614,0.97664887,0.011956887],"study_design_scores_gemma":[0.0107660545,0.00063876127,0.09453569,0.006913757,0.0006111712,0.0032589254,0.00079916656,0.0021435968,0.002338101,0.019105738,0.85854423,0.00034487058],"about_ca_topic_score_codex":0.008066981,"about_ca_topic_score_gemma":0.011276611,"teacher_disagreement_score":0.870145,"about_ca_system_score_codex":0.00090538483,"about_ca_system_score_gemma":0.0013056396,"threshold_uncertainty_score":0.18522239},"labels":[],"label_agreement":null},{"id":"W6902126386","doi":"10.6084/m9.figshare.28040104.v1","title":"Additional file 1 of Cognitive benefits of folic acid supplementation during pregnancy track with epigenetic changes at an imprint regulator","year":2024,"lang":"en","type":"article","venue":"Figshare","topic":"Genetic Syndromes and Imprinting","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":"University of British Columbia","funders":"","keywords":"Regulator; Epigenetics; EPIC; CpG site; Table (database); Offspring; Pregnancy; Folic acid; DNA methylation","score_opus":0.017674961586394373,"score_gpt":0.24242228909963967,"score_spread":0.2247473275132453,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W6902126386","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":[0.00021977481,0.00003754844,0.00036905264,0.00008422247,0.000028277525,0.00013471502,0.99811816,0.00021204221,0.0007962131],"genre_scores_gemma":[0.014085659,0.00045596773,0.008923946,0.0010647578,0.00017189531,0.0067912014,0.94719285,0.001298073,0.020015616],"study_design_codex":"not_applicable","study_design_gemma":"observational","domain_scores_codex":[0.9993579,0.00013916343,0.0001022411,0.0001672714,0.00015251675,0.000081002414],"domain_scores_gemma":[0.9816742,0.014804111,0.00081578793,0.00089475187,0.0014126019,0.000398562],"candidate_categories":["insufficient_payload"],"consensus_categories":[],"category_scores_codex":[0.0015667628,0.0012528021,0.0015825235,0.0015516438,0.00097373023,0.0014900855,0.0018443887,0.0012782874,0.9023862],"category_scores_gemma":[0.02471221,0.00057147007,0.0010457843,0.002465941,0.00026091727,0.0013229147,0.0008139687,0.0009030828,0.16463546],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0012369438,0.00023585277,0.0027062476,0.0069238422,0.000119775046,0.00012206428,0.000102168415,0.00050068024,0.0003188219,0.00082269567,0.96487904,0.02203196],"study_design_scores_gemma":[0.015087956,0.0014573354,0.045894053,0.008697705,0.000769516,0.001323987,0.00068666885,0.0026714797,0.0026390005,0.018885043,0.90158594,0.00030141117],"about_ca_topic_score_codex":0.0064756577,"about_ca_topic_score_gemma":0.011125669,"teacher_disagreement_score":0.9023862,"about_ca_system_score_codex":0.0010029227,"about_ca_system_score_gemma":0.0017484025,"threshold_uncertainty_score":0.13923419},"labels":[],"label_agreement":null},{"id":"W6902230824","doi":"10.6084/m9.figshare.28040116.v1","title":"Additional file 4 of Cognitive benefits of folic acid supplementation during pregnancy track with epigenetic changes at an imprint regulator","year":2024,"lang":"en","type":"article","venue":"Figshare","topic":"Genetic Syndromes and Imprinting","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":"University of British Columbia","funders":"","keywords":"Regulator; Track (disk drive); Epigenetics; Pregnancy; Folic acid; Folic acid supplementation","score_opus":0.0175098936779545,"score_gpt":0.24244197318072602,"score_spread":0.22493207950277153,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W6902230824","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":[0.00019489734,0.000026882584,0.00028461893,0.00009651661,0.000034223704,0.00007324636,0.9982343,0.00030342984,0.0007519256],"genre_scores_gemma":[0.009701387,0.0002514736,0.0055805296,0.0008164971,0.00014914316,0.0022906847,0.9665972,0.0012117215,0.013401269],"study_design_codex":"not_applicable","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9993886,0.00009428546,0.00009284681,0.00015822027,0.0001665837,0.00009958814],"domain_scores_gemma":[0.985482,0.011152625,0.0006955527,0.0007821408,0.0015384364,0.00034923555],"candidate_categories":["insufficient_payload"],"consensus_categories":[],"category_scores_codex":[0.0012465953,0.0013101965,0.0016510959,0.0016876109,0.0010529156,0.0016135874,0.0018116263,0.0014301288,0.9072376],"category_scores_gemma":[0.019210929,0.00063695415,0.0012745393,0.0025697374,0.00026362637,0.0013597899,0.00089163333,0.0009537752,0.17377222],"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":[0.0012465122,0.00021891779,0.0025554157,0.0048841108,0.00012205532,0.00015159944,0.000084247695,0.0005781629,0.0006021322,0.0007304828,0.97385186,0.014974468],"study_design_scores_gemma":[0.017349083,0.0011410626,0.06099871,0.00614681,0.0006300777,0.0012596333,0.0005680081,0.0028617845,0.003966995,0.016469369,0.88823736,0.00037108452],"about_ca_topic_score_codex":0.008704638,"about_ca_topic_score_gemma":0.013029305,"teacher_disagreement_score":0.9072376,"about_ca_system_score_codex":0.0011232054,"about_ca_system_score_gemma":0.0016340322,"threshold_uncertainty_score":0.13231432},"labels":[],"label_agreement":null},{"id":"W6902261421","doi":"10.6084/m9.figshare.26558375","title":"Additional file 1 of Genome-wide placental DNA methylations in fetal overgrowth and associations with leptin, adiponectin and fetal growth factors","year":2024,"lang":"en","type":"article","venue":"Figshare","topic":"Genetic Syndromes and Imprinting","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":"University of Toronto","funders":"","keywords":"Adiponectin; Fetus; Fetal growth; DNA; Mutation","score_opus":0.010948731234723045,"score_gpt":0.21346683007641326,"score_spread":0.20251809884169023,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W6902261421","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":[0.00031735556,0.00002472526,0.00024445463,0.00006904649,0.00001458462,0.00003524505,0.9987295,0.0001678581,0.00039719226],"genre_scores_gemma":[0.017792048,0.00025637695,0.0045166556,0.00058536744,0.00012374934,0.001805311,0.9647836,0.0008517713,0.009285167],"study_design_codex":"not_applicable","study_design_gemma":"observational","domain_scores_codex":[0.9993432,0.00013606873,0.00010500027,0.00019394212,0.0001204004,0.00010139387],"domain_scores_gemma":[0.9766666,0.019522576,0.0010879745,0.0008948124,0.0013662281,0.0004617612],"candidate_categories":["insufficient_payload"],"consensus_categories":[],"category_scores_codex":[0.0014859367,0.0011214766,0.0013863365,0.0021842665,0.0009694111,0.0015396843,0.0019055215,0.0010720938,0.8439314],"category_scores_gemma":[0.028852781,0.0005601397,0.0010368155,0.0036910204,0.00027071548,0.0013062821,0.0008891188,0.00087751506,0.11167275],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0004992312,0.0001420569,0.00923224,0.0039863745,0.00014168849,0.00018200191,0.00014317423,0.00069480663,0.00021499433,0.0007808371,0.97091866,0.013064015],"study_design_scores_gemma":[0.012326254,0.00079389755,0.1479633,0.007376283,0.0009495917,0.0027769946,0.0012306562,0.005510718,0.001897231,0.020324325,0.79848546,0.0003653531],"about_ca_topic_score_codex":0.010071843,"about_ca_topic_score_gemma":0.015517554,"teacher_disagreement_score":0.8439314,"about_ca_system_score_codex":0.0007292305,"about_ca_system_score_gemma":0.0014711532,"threshold_uncertainty_score":0.22261298},"labels":[],"label_agreement":null},{"id":"W6902356380","doi":"10.6084/m9.figshare.26558375.v1","title":"Additional file 1 of Genome-wide placental DNA methylations in fetal overgrowth and associations with leptin, adiponectin and fetal growth factors","year":2024,"lang":"en","type":"article","venue":"Figshare","topic":"Genetic Syndromes and Imprinting","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":"University of Toronto","funders":"","keywords":"Adiponectin; Fetus; Fetal growth; DNA; Mutation","score_opus":0.010948731234723045,"score_gpt":0.21346683007641326,"score_spread":0.20251809884169023,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W6902356380","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":[0.00031735556,0.00002472526,0.00024445463,0.00006904649,0.00001458462,0.00003524505,0.9987295,0.0001678581,0.00039719226],"genre_scores_gemma":[0.017792048,0.00025637695,0.0045166556,0.00058536744,0.00012374934,0.001805311,0.9647836,0.0008517713,0.009285167],"study_design_codex":"not_applicable","study_design_gemma":"observational","domain_scores_codex":[0.9993432,0.00013606873,0.00010500027,0.00019394212,0.0001204004,0.00010139387],"domain_scores_gemma":[0.9766666,0.019522576,0.0010879745,0.0008948124,0.0013662281,0.0004617612],"candidate_categories":["insufficient_payload"],"consensus_categories":[],"category_scores_codex":[0.0014859367,0.0011214766,0.0013863365,0.0021842665,0.0009694111,0.0015396843,0.0019055215,0.0010720938,0.8439314],"category_scores_gemma":[0.028852781,0.0005601397,0.0010368155,0.0036910204,0.00027071548,0.0013062821,0.0008891188,0.00087751506,0.11167275],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0004992312,0.0001420569,0.00923224,0.0039863745,0.00014168849,0.00018200191,0.00014317423,0.00069480663,0.00021499433,0.0007808371,0.97091866,0.013064015],"study_design_scores_gemma":[0.012326254,0.00079389755,0.1479633,0.007376283,0.0009495917,0.0027769946,0.0012306562,0.005510718,0.001897231,0.020324325,0.79848546,0.0003653531],"about_ca_topic_score_codex":0.010071843,"about_ca_topic_score_gemma":0.015517554,"teacher_disagreement_score":0.8439314,"about_ca_system_score_codex":0.0007292305,"about_ca_system_score_gemma":0.0014711532,"threshold_uncertainty_score":0.22261298},"labels":[],"label_agreement":null},{"id":"W6906496455","doi":"10.17605/osf.io/9r4wf","title":"Sex-dependent placental mQTL provide insight into the prenatal origins of childhood-onset traits and conditions","year":2022,"lang":"en","type":"article","venue":"OSF Preprints (OSF Preprints)","topic":"Genetic Syndromes and Imprinting","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":"University of British Columbia","funders":"","keywords":"Pregnancy; Offspring; Fetus; Placenta","score_opus":0.006172744144943737,"score_gpt":0.22861543610749452,"score_spread":0.2224426919625508,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W6906496455","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9191983,0.024091067,0.018044502,0.0018627916,0.0002863453,0.000042479845,0.03020215,0.00037170885,0.0059007443],"genre_scores_gemma":[0.98798466,0.0028669517,0.002748169,0.0003544897,0.00008432436,0.000043828462,0.0041513094,0.00023233729,0.0015338927],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.998052,0.0005394805,0.00012294536,0.0008850137,0.00021438125,0.00018620705],"domain_scores_gemma":[0.99706906,0.0017108204,0.00043314535,0.00051933667,0.00013285334,0.0001348063],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0021051483,0.0009382612,0.0009676929,0.00146011,0.00055590394,0.00179783,0.00082838774,0.0009264453,0.008947903],"category_scores_gemma":[0.007817723,0.0006408576,0.0025466948,0.0021241575,0.00056428654,0.00060103514,0.0015262899,0.0013878597,0.0005588476],"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":[0.0027967852,0.000029243432,0.9020948,0.0011979333,0.015792608,0.0018027232,0.0013731294,0.0018436552,0.029248975,0.003644022,0.003923714,0.03625235],"study_design_scores_gemma":[0.00012430959,0.00017207731,0.9681188,0.00033321013,0.009405394,0.0019985756,0.0004336101,0.001098757,0.0038960634,0.0051546847,0.009220338,0.000044208115],"about_ca_topic_score_codex":0.0066632703,"about_ca_topic_score_gemma":0.007882037,"teacher_disagreement_score":0.008947903,"about_ca_system_score_codex":0.00035761885,"about_ca_system_score_gemma":0.0004203205,"threshold_uncertainty_score":0.02993375},"labels":[],"label_agreement":null},{"id":"W6920790104","doi":"10.6084/m9.figshare.20064368.v1","title":"Additional file 8 of Gain and loss of TASK3 channel function and its regulation by novel variation cause KCNK9 imprinting syndrome","year":2022,"lang":"en","type":"article","venue":"Figshare","topic":"Genetic Syndromes and Imprinting","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":"BC Children's Hospital","funders":"","keywords":"Function (biology); Extracellular; Channel (broadcasting); Loss function; HEK 293 cells; Gene; Variation (astronomy)","score_opus":0.013470722356893429,"score_gpt":0.2027671882946675,"score_spread":0.18929646593777408,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W6920790104","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":[0.00036332,0.000035474382,0.0002752616,0.00014654978,0.000043499906,0.00007091538,0.997979,0.0002504331,0.0008355344],"genre_scores_gemma":[0.020840263,0.00036225616,0.004198952,0.0011445116,0.00027760898,0.0016548019,0.95555425,0.0011390274,0.014828267],"study_design_codex":"not_applicable","study_design_gemma":"not_applicable","domain_scores_codex":[0.99916494,0.0001243203,0.00017734594,0.000215052,0.00019668615,0.00012175238],"domain_scores_gemma":[0.977417,0.017567877,0.001398427,0.0011764026,0.0018571644,0.00058314204],"candidate_categories":["insufficient_payload"],"consensus_categories":[],"category_scores_codex":[0.0013326039,0.0011378472,0.001593683,0.0021730133,0.00095820596,0.0015476326,0.0021133067,0.0015366019,0.8684674],"category_scores_gemma":[0.029724455,0.00063323765,0.0012408758,0.0030974138,0.00033197133,0.0014597026,0.0008990532,0.00090818154,0.1335],"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":[0.00078693446,0.00013584016,0.006121998,0.003943893,0.00013004028,0.00041578023,0.00011048277,0.0005337632,0.00039172603,0.0007595644,0.97346115,0.013208877],"study_design_scores_gemma":[0.013930187,0.00075411494,0.10398772,0.00824878,0.00079299405,0.003639277,0.00084942894,0.0026521184,0.0025471812,0.020528372,0.8416834,0.0003865174],"about_ca_topic_score_codex":0.008035134,"about_ca_topic_score_gemma":0.011307563,"teacher_disagreement_score":0.8684674,"about_ca_system_score_codex":0.0008972432,"about_ca_system_score_gemma":0.001331431,"threshold_uncertainty_score":0.18761533},"labels":[],"label_agreement":null},{"id":"W6920793839","doi":"10.6084/m9.figshare.28040107","title":"Additional file 2 of Cognitive benefits of folic acid supplementation during pregnancy track with epigenetic changes at an imprint regulator","year":2024,"lang":"en","type":"article","venue":"Figshare","topic":"Genetic Syndromes and Imprinting","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":"University of British Columbia","funders":"","keywords":"Methylation; DNA methylation; Epigenetics; Cord blood; Genotype; Table (database); Regulator","score_opus":0.01710101841153143,"score_gpt":0.24193957841293662,"score_spread":0.22483856000140517,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W6920793839","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":[0.0002703609,0.00002818765,0.00026978677,0.00010627716,0.000027411725,0.000091416,0.998279,0.00018193857,0.000745654],"genre_scores_gemma":[0.01964826,0.00032495428,0.0073906966,0.0012065999,0.00020312227,0.00443182,0.9459118,0.0011525518,0.01973021],"study_design_codex":"not_applicable","study_design_gemma":"observational","domain_scores_codex":[0.9994099,0.000112937334,0.00010284965,0.00016511237,0.00011916383,0.00009012191],"domain_scores_gemma":[0.9829874,0.0134385405,0.00086702453,0.0008934556,0.0014202823,0.0003933402],"candidate_categories":["insufficient_payload"],"consensus_categories":[],"category_scores_codex":[0.00128203,0.0011525479,0.0014778599,0.0013562002,0.0010286974,0.0016621589,0.001768995,0.0014196127,0.88064367],"category_scores_gemma":[0.030328637,0.0005557866,0.001190203,0.002204599,0.00022804657,0.0015058618,0.00086051313,0.0008308004,0.13492261],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0010095433,0.00014795217,0.005191431,0.0049952604,0.00013205678,0.000167662,0.0001207335,0.00045834886,0.0001733875,0.00082719175,0.96989083,0.016885635],"study_design_scores_gemma":[0.016122352,0.00093449233,0.08202726,0.010959258,0.0007620738,0.0017451191,0.0009940648,0.0033603227,0.0017403509,0.024307696,0.8567027,0.00034432192],"about_ca_topic_score_codex":0.010334013,"about_ca_topic_score_gemma":0.016123481,"teacher_disagreement_score":0.88064367,"about_ca_system_score_codex":0.00095956225,"about_ca_system_score_gemma":0.001567888,"threshold_uncertainty_score":0.17024732},"labels":[],"label_agreement":null},{"id":"W6920795910","doi":"10.6084/m9.figshare.26986429","title":"Additional file 10 of Conservation and divergence of canonical and non-canonical imprinting in murids","year":2024,"lang":"en","type":"article","venue":"Figshare","topic":"Genetic Syndromes and Imprinting","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":"BC Children's Hospital; University of British Columbia","funders":"","keywords":"Imprinting (psychology); Divergence (linguistics); Entropy (arrow of time); Genome","score_opus":0.013896958573758356,"score_gpt":0.2409133182193833,"score_spread":0.22701635964562494,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W6920795910","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":[0.00009826995,0.00023303382,0.00027976758,0.0003404332,0.00015037,0.00004716793,0.9952976,0.0004168238,0.0031365578],"genre_scores_gemma":[0.008341538,0.0015774881,0.0036394838,0.001389151,0.0005094426,0.0009875275,0.946382,0.0018617779,0.035311554],"study_design_codex":"not_applicable","study_design_gemma":"observational","domain_scores_codex":[0.9991007,0.00019155115,0.00013291309,0.00021458481,0.00026110027,0.00009925818],"domain_scores_gemma":[0.97554463,0.018168097,0.001240805,0.0012914038,0.0030971812,0.0006578796],"candidate_categories":["insufficient_payload"],"consensus_categories":[],"category_scores_codex":[0.0021007054,0.0007914229,0.0014525461,0.0040774834,0.0008474668,0.0018629753,0.0019333056,0.0012264252,0.9006961],"category_scores_gemma":[0.031019615,0.0005366236,0.0008741882,0.005935468,0.00033690574,0.0025125006,0.0012345038,0.0008869857,0.27457994],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00007750271,0.000009508304,0.00049057713,0.002428878,0.00002020397,0.00003684587,0.000042371492,0.000093919516,0.00005306331,0.0007257973,0.98876065,0.007260681],"study_design_scores_gemma":[0.0004251272,0.00003970067,0.0074444264,0.0027181464,0.000070809205,0.00025058645,0.0001318517,0.00015781034,0.00017941016,0.0042377478,0.98429316,0.000051068924],"about_ca_topic_score_codex":0.0066773486,"about_ca_topic_score_gemma":0.00923858,"teacher_disagreement_score":0.9006961,"about_ca_system_score_codex":0.0013634837,"about_ca_system_score_gemma":0.0019275711,"threshold_uncertainty_score":0.14164495},"labels":[],"label_agreement":null},{"id":"W6921018293","doi":"10.6084/m9.figshare.28040110","title":"Additional file 3 of Cognitive benefits of folic acid supplementation during pregnancy track with epigenetic changes at an imprint regulator","year":2024,"lang":"en","type":"article","venue":"Figshare","topic":"Genetic Syndromes and Imprinting","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":"University of British Columbia","funders":"","keywords":"Cognition; Regulator; Pregnancy; Epigenetics; Folic acid; Track (disk drive); Folic acid supplementation","score_opus":0.01738066982375489,"score_gpt":0.24208178526760682,"score_spread":0.22470111544385193,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W6921018293","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":[0.00027135192,0.000023164022,0.00023477776,0.000080408085,0.000018139115,0.00007498469,0.99844724,0.00014684789,0.00070303044],"genre_scores_gemma":[0.020899698,0.00028543963,0.0063668815,0.001029485,0.0001602803,0.0042463313,0.9485904,0.0010875385,0.017333878],"study_design_codex":"not_applicable","study_design_gemma":"not_applicable","domain_scores_codex":[0.99935156,0.00012415253,0.00011240564,0.00017715455,0.00013611115,0.00009847665],"domain_scores_gemma":[0.97942746,0.016571375,0.0010474039,0.000985143,0.0016139812,0.0003547247],"candidate_categories":["insufficient_payload"],"consensus_categories":["insufficient_payload"],"category_scores_codex":[0.0014168978,0.0012669928,0.0014766313,0.0014213794,0.0010320466,0.0016584914,0.0017417977,0.001399809,0.87396944],"category_scores_gemma":[0.030679658,0.0005809297,0.0014119503,0.0024591591,0.00025070325,0.0014658915,0.00083160505,0.00090429856,0.11898084],"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":[0.0014699614,0.00018014824,0.006223294,0.004548693,0.00019140121,0.00016698371,0.00011593437,0.0006083385,0.00020345757,0.00085556705,0.97017324,0.015262951],"study_design_scores_gemma":[0.025439434,0.0012739368,0.1078829,0.011490876,0.0012684988,0.0019449649,0.0010225906,0.004119156,0.002177496,0.027115805,0.81585944,0.00040495626],"about_ca_topic_score_codex":0.013259495,"about_ca_topic_score_gemma":0.018742058,"teacher_disagreement_score":0.12603056,"about_ca_system_score_codex":0.0010844175,"about_ca_system_score_gemma":0.001523713,"threshold_uncertainty_score":0.17976725},"labels":[],"label_agreement":null},{"id":"W6921028860","doi":"10.6084/m9.figshare.26986399","title":"Additional file 1 of Conservation and divergence of canonical and non-canonical imprinting in murids","year":2024,"lang":"en","type":"article","venue":"Figshare","topic":"Genetic Syndromes and Imprinting","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":"BC Children's Hospital; University of British Columbia","funders":"","keywords":"Imprinting (psychology); Divergence (linguistics); Entropy (arrow of time); Genome","score_opus":0.012503434411400817,"score_gpt":0.23530005347426144,"score_spread":0.22279661906286063,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W6921028860","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":[0.00019643441,0.0000194448,0.00025083742,0.000049315953,0.000023044327,0.00002080609,0.99801564,0.00031364814,0.0011109087],"genre_scores_gemma":[0.00746966,0.00015716649,0.0033486893,0.00025108788,0.00006651682,0.00043104895,0.9789853,0.0012341271,0.008056281],"study_design_codex":"not_applicable","study_design_gemma":"not_applicable","domain_scores_codex":[0.9994246,0.00008647945,0.0000686722,0.0001679368,0.00016213644,0.00009023933],"domain_scores_gemma":[0.98693347,0.00977632,0.0006459563,0.0008610201,0.0013808435,0.00040240827],"candidate_categories":["insufficient_payload"],"consensus_categories":[],"category_scores_codex":[0.0012110798,0.0009584726,0.0012026723,0.0029944626,0.0011732354,0.0015552953,0.0018794144,0.0010190872,0.8735932],"category_scores_gemma":[0.015687738,0.00055991905,0.00072796614,0.0052188532,0.00033210838,0.0016783695,0.0010232169,0.00090722594,0.2548374],"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":[0.0001837932,0.00005740006,0.0026474653,0.0018939999,0.000039487786,0.00007235152,0.00009529975,0.00039186864,0.00033940646,0.0010427504,0.9842107,0.009025507],"study_design_scores_gemma":[0.0016385816,0.00016960296,0.03443063,0.0019838705,0.00014850112,0.0006695376,0.0004246258,0.0013218025,0.0011852969,0.009817146,0.94807893,0.0001315381],"about_ca_topic_score_codex":0.0068303957,"about_ca_topic_score_gemma":0.011106966,"teacher_disagreement_score":0.8735932,"about_ca_system_score_codex":0.001005254,"about_ca_system_score_gemma":0.0013296993,"threshold_uncertainty_score":0.18030387},"labels":[],"label_agreement":null},{"id":"W6921174781","doi":"10.6084/m9.figshare.28040110.v1","title":"Additional file 3 of Cognitive benefits of folic acid supplementation during pregnancy track with epigenetic changes at an imprint regulator","year":2024,"lang":"en","type":"article","venue":"Figshare","topic":"Genetic Syndromes and Imprinting","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":"University of British Columbia","funders":"","keywords":"Cognition; Regulator; Pregnancy; Epigenetics; Folic acid; Track (disk drive); Folic acid supplementation","score_opus":0.01738066982375489,"score_gpt":0.24208178526760682,"score_spread":0.22470111544385193,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W6921174781","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":[0.00027135192,0.000023164022,0.00023477776,0.000080408085,0.000018139115,0.00007498469,0.99844724,0.00014684789,0.00070303044],"genre_scores_gemma":[0.020899698,0.00028543963,0.0063668815,0.001029485,0.0001602803,0.0042463313,0.9485904,0.0010875385,0.017333878],"study_design_codex":"not_applicable","study_design_gemma":"not_applicable","domain_scores_codex":[0.99935156,0.00012415253,0.00011240564,0.00017715455,0.00013611115,0.00009847665],"domain_scores_gemma":[0.97942746,0.016571375,0.0010474039,0.000985143,0.0016139812,0.0003547247],"candidate_categories":["insufficient_payload"],"consensus_categories":[],"category_scores_codex":[0.0014168978,0.0012669928,0.0014766313,0.0014213794,0.0010320466,0.0016584914,0.0017417977,0.001399809,0.87396944],"category_scores_gemma":[0.030679658,0.0005809297,0.0014119503,0.0024591591,0.00025070325,0.0014658915,0.00083160505,0.00090429856,0.11898084],"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":[0.0014699614,0.00018014824,0.006223294,0.004548693,0.00019140121,0.00016698371,0.00011593437,0.0006083385,0.00020345757,0.00085556705,0.97017324,0.015262951],"study_design_scores_gemma":[0.025439434,0.0012739368,0.1078829,0.011490876,0.0012684988,0.0019449649,0.0010225906,0.004119156,0.002177496,0.027115805,0.81585944,0.00040495626],"about_ca_topic_score_codex":0.013259495,"about_ca_topic_score_gemma":0.018742058,"teacher_disagreement_score":0.87396944,"about_ca_system_score_codex":0.0010844175,"about_ca_system_score_gemma":0.001523713,"threshold_uncertainty_score":0.17976725},"labels":[],"label_agreement":null},{"id":"W6924816004","doi":"10.15468/dl.xt8vn7","title":"Occurrence Download","year":2022,"lang":"en","type":"dataset","venue":"Global Biodiversity Information Facility","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":0,"is_retracted":false,"has_abstract":true,"route_ca_aff":false,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":true,"ca_institutions":"","funders":"","keywords":"Download; Matching (statistics); Range (aeronautics); Alien; The Internet","score_opus":0.010486658535468119,"score_gpt":0.21445995961899314,"score_spread":0.20397330108352502,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W6924816004","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":[0.000044426295,0.00003195271,0.00004222821,0.00003969728,0.000010817057,0.0000059489303,0.9988391,0.0004157905,0.00056995684],"genre_scores_gemma":[0.00016761298,0.000038351463,0.00019687803,0.00004782262,0.0000034054835,0.000043594926,0.99894065,0.00013517353,0.00042655368],"study_design_codex":"not_applicable","study_design_gemma":"not_applicable","domain_scores_codex":[0.99901843,0.00013808753,0.00012448573,0.00035307603,0.00021184239,0.00015407143],"domain_scores_gemma":[0.9977336,0.0007074527,0.00020185123,0.000572556,0.00051737914,0.00026716499],"candidate_categories":["insufficient_payload"],"consensus_categories":[],"category_scores_codex":[0.0009817731,0.002228395,0.001752411,0.004785733,0.0010596092,0.0026960096,0.003016921,0.0023296978,0.14927562],"category_scores_gemma":[0.006012252,0.00092087244,0.0012466582,0.008924883,0.0004608896,0.0022828216,0.002479132,0.0020783946,0.2117231],"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":[0.000035368263,0.000013630922,0.0004019882,0.00060812605,0.000017129254,0.000018167482,0.00002197861,0.00015707847,0.00011667438,0.0003707227,0.9968172,0.0014219251],"study_design_scores_gemma":[0.000105138264,0.000010321149,0.0018920484,0.00021394415,0.00001742695,0.000044315522,0.00007219655,0.00022897913,0.00021082681,0.0009176188,0.9962669,0.000020278912],"about_ca_topic_score_codex":0.021610225,"about_ca_topic_score_gemma":0.034828827,"teacher_disagreement_score":0.8507244,"about_ca_system_score_codex":0.0016952148,"about_ca_system_score_gemma":0.0023948448,"threshold_uncertainty_score":0.49937665},"labels":[],"label_agreement":null},{"id":"W6929020360","doi":"10.4224/23001184","title":"Winter solstice, 2016","year":2016,"lang":"en","type":"article","venue":"NPARC","topic":"Genetic Syndromes and Imprinting","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":true,"route_about_ca":false,"ca_institutions":"Herzberg Institute of Astrophysics","funders":"","keywords":"","score_opus":0.008009952740876309,"score_gpt":0.2285688314137787,"score_spread":0.2205588786729024,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W6929020360","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":[0.006252074,0.0041263867,0.0019421672,0.03395489,0.13701768,0.0012984932,0.009774783,0.0028371047,0.8027965],"genre_scores_gemma":[0.0041689365,0.00049340416,0.00032561086,0.0005127441,0.0022429174,0.00007391184,0.0014167598,0.00035379562,0.99041194],"study_design_codex":"not_applicable","study_design_gemma":"not_applicable","domain_scores_codex":[0.99620134,0.0006163302,0.00017017941,0.00045521156,0.0019844426,0.00057249016],"domain_scores_gemma":[0.98935,0.000759854,0.0002645457,0.0014887089,0.005348326,0.0027885598],"candidate_categories":["insufficient_payload"],"consensus_categories":[],"category_scores_codex":[0.0039341087,0.00082345796,0.0011816077,0.0023472435,0.0032133074,0.0073566167,0.0020467143,0.0025959057,0.6263133],"category_scores_gemma":[0.013814476,0.000612674,0.0008862578,0.0009596586,0.0012753286,0.0017616742,0.0041727345,0.0026162646,0.48870724],"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":[0.0002163031,0.000047917347,0.00036945313,0.00020520789,0.000020063699,0.00016730046,0.00007035278,0.0000753735,0.0007797684,0.0017412422,0.9634096,0.032897286],"study_design_scores_gemma":[0.000028582155,0.00003155214,0.0009443354,0.00012872566,0.000004657408,0.000076741315,0.00008696775,0.0001345178,0.00059990527,0.00076482596,0.9971884,0.000010771984],"about_ca_topic_score_codex":0.0026645178,"about_ca_topic_score_gemma":0.012287422,"teacher_disagreement_score":0.6263133,"about_ca_system_score_codex":0.0026609038,"about_ca_system_score_gemma":0.004096494,"threshold_uncertainty_score":0.5330187},"labels":[],"label_agreement":null},{"id":"W6929956472","doi":"10.5281/zenodo.10445082","title":"Counting is not Enough. Modelling Relevance in Art Exhibition Ecosystems","year":2020,"lang":"en","type":"article","venue":"Zenodo (CERN European Organization for Nuclear Research)","topic":"Genetic Syndromes and Imprinting","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":"Western University","funders":"","keywords":"Relevance (law); Exhibition; Leverage (statistics); Interpretation (philosophy); Institution; Data collection; Value (mathematics)","score_opus":0.03607981117598916,"score_gpt":0.22888931049986377,"score_spread":0.19280949932387462,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W6929956472","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":[0.29353964,0.0015356683,0.653719,0.004542008,0.00015197622,0.00027942695,0.0009072652,0.0005498372,0.044775113],"genre_scores_gemma":[0.931207,0.00042666274,0.058843706,0.0001544127,0.00007868328,0.00024963773,0.00030845025,0.00013732242,0.008594131],"study_design_codex":"theoretical_or_conceptual","study_design_gemma":"simulation_or_modeling","domain_scores_codex":[0.99634933,0.0017253385,0.00018318639,0.0008346555,0.00054252945,0.00036499475],"domain_scores_gemma":[0.97954535,0.014606954,0.0029983958,0.0011668062,0.0009171727,0.00076532667],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0067275474,0.0008430009,0.0010407591,0.0036268514,0.0017455078,0.006265085,0.0024563312,0.0026995298,0.005770759],"category_scores_gemma":[0.035948925,0.0008495399,0.0019240471,0.0044069574,0.004105743,0.009092676,0.003227909,0.0020791118,0.00073230825],"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":[0.00007961529,0.00011704609,0.019681776,0.00017493438,0.00010370451,0.00031449774,0.0010233843,0.40889785,0.000600113,0.53749406,0.0021907866,0.029322257],"study_design_scores_gemma":[0.000013387331,0.000029876543,0.0037618405,0.000043439075,0.000031832424,0.00013391692,0.00033422638,0.64574414,0.00023532107,0.34517366,0.004462225,0.000036099016],"about_ca_topic_score_codex":0.013418871,"about_ca_topic_score_gemma":0.011293999,"teacher_disagreement_score":0.013418871,"about_ca_system_score_codex":0.0043847505,"about_ca_system_score_gemma":0.001775772,"threshold_uncertainty_score":0.035579085},"labels":[],"label_agreement":null},{"id":"W6929982221","doi":"10.5281/zenodo.10943409","title":"Neognathus terrestris","year":2023,"lang":"en","type":"article","venue":"Zenodo (CERN European Organization for Nuclear Research)","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":0,"is_retracted":false,"has_abstract":true,"route_ca_aff":false,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":true,"ca_institutions":"","funders":"","keywords":"Lumbricus terrestris; Litter; Bombus terrestris; Distribution (mathematics)","score_opus":0.027199308787913417,"score_gpt":0.2471511671842255,"score_spread":0.2199518583963121,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W6929982221","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9017076,0.0034233346,0.000936843,0.00028399812,0.000086626096,0.00011140782,0.0033692932,0.0002273153,0.08985356],"genre_scores_gemma":[0.95420563,0.0020015945,0.0025180418,0.00033542898,0.00004460625,0.00014215964,0.0046559735,0.000027397979,0.036069166],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.99994624,0.000005816211,0.0000045348434,0.000023976512,0.000012241778,0.0000071219583],"domain_scores_gemma":[0.9999193,0.00001328381,0.000025407164,0.000013479315,0.00001289005,0.000015680405],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00008553773,0.0003738514,0.0001689051,0.00093048456,0.00057285686,0.00012977133,0.00037804386,0.00023990477,0.0064119026],"category_scores_gemma":[0.00014320332,0.00014212294,0.00009777795,0.0004759657,0.00042262007,0.00023579206,0.00049283984,0.0002156782,0.0024511968],"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":[0.0010614666,0.00027045066,0.42001304,0.0009405611,0.00017893614,0.005749409,0.0040316363,0.0010118689,0.11506535,0.0041444646,0.017932363,0.42960042],"study_design_scores_gemma":[0.00004968611,0.0002659903,0.91778046,0.00022251763,0.000054323085,0.003977703,0.0016493065,0.00015755856,0.0024408444,0.0010968999,0.072278775,0.000025965215],"about_ca_topic_score_codex":0.014627693,"about_ca_topic_score_gemma":0.04290991,"teacher_disagreement_score":0.014627693,"about_ca_system_score_codex":0.00026082998,"about_ca_system_score_gemma":0.00015527302,"threshold_uncertainty_score":0.0290851},"labels":[],"label_agreement":null},{"id":"W6930041778","doi":"10.5281/zenodo.12129107","title":"Walter benjamin flaneur pdf","year":2024,"lang":"en","type":"other","venue":"Zenodo (CERN European Organization for Nuclear Research)","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":0,"is_retracted":false,"has_abstract":true,"route_ca_aff":false,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":true,"ca_institutions":"","funders":"","keywords":"Modernity; Capital (architecture); Architecture; Publishing; Diversity (politics); Key (lock); Modernism (music); Product (mathematics); Late modernity","score_opus":0.016527927299610664,"score_gpt":0.2351124061943877,"score_spread":0.21858447889477703,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W6930041778","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":[0.00028743202,0.003202638,0.0016943755,0.006600712,0.0072870324,0.00010013317,0.0015045487,0.0034436083,0.97587943],"genre_scores_gemma":[0.00078571035,0.0012273986,0.00041983492,0.0009549805,0.00064672355,0.00002709978,0.00040509252,0.0006217265,0.9949115],"study_design_codex":"not_applicable","study_design_gemma":"not_applicable","domain_scores_codex":[0.9990126,0.00007034375,0.00003384239,0.00013854366,0.00065025233,0.00009442399],"domain_scores_gemma":[0.998401,0.00020361645,0.00006345386,0.00019418418,0.0007482467,0.000389508],"candidate_categories":["insufficient_payload"],"consensus_categories":["insufficient_payload"],"category_scores_codex":[0.00085424265,0.0013441446,0.0008230826,0.0021562562,0.0020924858,0.006744763,0.0014503505,0.0025707348,0.80095595],"category_scores_gemma":[0.0042521413,0.0006232124,0.0007247577,0.0014198296,0.00072314194,0.0056851767,0.0030997058,0.0027461776,0.7613775],"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":[0.000010460393,0.000009905402,0.00002200239,0.000049960607,8.8594317e-7,0.000034307734,0.000027279773,0.00002425957,0.00016212357,0.0018771767,0.9578264,0.03995526],"study_design_scores_gemma":[0.0000014784231,0.0000033912745,0.000046349716,0.00003305125,6.0255206e-7,0.000044017237,0.00002199025,0.00001800432,0.00006674321,0.0003032897,0.9994579,0.0000031010852],"about_ca_topic_score_codex":0.0035373834,"about_ca_topic_score_gemma":0.0075262757,"teacher_disagreement_score":0.19904405,"about_ca_system_score_codex":0.0014766199,"about_ca_system_score_gemma":0.0014593746,"threshold_uncertainty_score":0.28391218},"labels":[],"label_agreement":null},{"id":"W6930168875","doi":"10.5281/zenodo.11670281","title":"[+[!LIVE!]+] 24 Hours of Le Mans 2024 Live Streams FREE On TV Channel 15-16 June 2024","year":2024,"lang":"en","type":"other","venue":"Zenodo (CERN European Organization for Nuclear Research)","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":0,"is_retracted":false,"has_abstract":true,"route_ca_aff":false,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":true,"ca_institutions":"","funders":"","keywords":"Channel (broadcasting); Test (biology); STREAMS; Time lag; Daylight","score_opus":0.018156951389832744,"score_gpt":0.2304228953282263,"score_spread":0.21226594393839354,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W6930168875","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":[0.0022356666,0.00016086956,0.00050155784,0.000657052,0.0024735203,0.0002393046,0.0050685457,0.0035809323,0.9850825],"genre_scores_gemma":[0.0059167338,0.000192933,0.0002766061,0.0003467866,0.0004811743,0.00010638831,0.0024273947,0.00081797515,0.98943406],"study_design_codex":"not_applicable","study_design_gemma":"not_applicable","domain_scores_codex":[0.9997576,0.000018363055,0.0000062083186,0.000034400335,0.000082559825,0.0001008835],"domain_scores_gemma":[0.99906415,0.000028935337,0.000024358842,0.00005920957,0.00036947164,0.0004539184],"candidate_categories":["insufficient_payload"],"consensus_categories":["insufficient_payload"],"category_scores_codex":[0.00032403955,0.0009778072,0.0005925061,0.0007159509,0.0028962258,0.0025615592,0.00074330077,0.0011442886,0.8522894],"category_scores_gemma":[0.0011203368,0.00038771168,0.0004958627,0.00051119283,0.00036665754,0.0014119094,0.00311967,0.0011191112,0.732652],"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":[0.00006647248,0.000032852364,0.00028800682,0.00004331193,0.000003302304,0.000053463616,0.000065480686,0.00002779129,0.00043121356,0.00029457337,0.9862816,0.012411888],"study_design_scores_gemma":[0.000028246926,0.00005415959,0.0036173915,0.00006589647,0.0000046597766,0.000046150668,0.0002929675,0.00005669552,0.00024232795,0.00008789469,0.9954913,0.000012304279],"about_ca_topic_score_codex":0.009235896,"about_ca_topic_score_gemma":0.03775993,"teacher_disagreement_score":0.14771062,"about_ca_system_score_codex":0.000605929,"about_ca_system_score_gemma":0.0006074283,"threshold_uncertainty_score":0.21069127},"labels":[],"label_agreement":null},{"id":"W6930601871","doi":"10.5281/zenodo.13356387","title":"Certainement ! Voici dix titres captivants pour VeeloBooster Avis","year":2024,"lang":"fr","type":"other","venue":"Zenodo (CERN European Organization for Nuclear Research)","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":0,"is_retracted":false,"has_abstract":true,"route_ca_aff":false,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":true,"ca_institutions":"","funders":"","keywords":"Nucleofection; Gloom; Limiting; Laziness","score_opus":0.022631854584985532,"score_gpt":0.2446868193546193,"score_spread":0.22205496476963377,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W6930601871","genre_codex":"review","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":[0.28465557,0.3972723,0.01055195,0.022438081,0.018844815,0.0020505127,0.0034497443,0.0024766596,0.25826037],"genre_scores_gemma":[0.4296114,0.12571144,0.025316425,0.010739353,0.0035666882,0.0015736102,0.0036100973,0.00070373854,0.39916727],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.99973994,0.000048346006,0.00002411492,0.00003804763,0.000105644525,0.000043972716],"domain_scores_gemma":[0.9998222,0.000058416677,0.000015647707,0.000010574933,0.00004550229,0.000047741865],"candidate_categories":["insufficient_payload"],"consensus_categories":[],"category_scores_codex":[0.000499446,0.000595076,0.00065318716,0.00062953203,0.00070429454,0.0009372316,0.0005153219,0.0012446287,0.06186927],"category_scores_gemma":[0.00094560377,0.000226128,0.0008485795,0.0003157134,0.00024696358,0.00072025816,0.0004532935,0.0017752202,0.013254298],"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":[0.008805883,0.0030646177,0.0014715322,0.003161201,0.00015171964,0.0017243935,0.0004982075,0.0002815317,0.043891802,0.0015806005,0.07268891,0.86267966],"study_design_scores_gemma":[0.0018695907,0.01255282,0.00789673,0.0014939383,0.00026106942,0.0042755567,0.0006043184,0.00065369986,0.033967607,0.0008629628,0.93548,0.00008180406],"about_ca_topic_score_codex":0.0023823788,"about_ca_topic_score_gemma":0.0049104425,"teacher_disagreement_score":0.93813074,"about_ca_system_score_codex":0.0003911005,"about_ca_system_score_gemma":0.000388634,"threshold_uncertainty_score":0.20697331},"labels":[],"label_agreement":null},{"id":"W6930757390","doi":"10.5281/zenodo.16794414","title":"CanPests V1","year":2025,"lang":"en","type":"dataset","venue":"Zenodo (CERN European Organization for Nuclear Research)","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":0,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":true,"ca_institutions":"University of Guelph","funders":"Genome Canada","keywords":"Barcode; DNA barcoding; Identifier; Host (biology); Identification (biology)","score_opus":0.01664895475827676,"score_gpt":0.24944338761015736,"score_spread":0.2327944328518806,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W6930757390","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":[0.000118900534,0.000037059453,0.000035552515,0.00002390594,0.0000074204618,0.000009051339,0.9990017,0.00023604331,0.0005303937],"genre_scores_gemma":[0.00034088723,0.00004321886,0.00024823277,0.00002577226,0.00000195181,0.00003995826,0.99879336,0.000073713214,0.0004328294],"study_design_codex":"not_applicable","study_design_gemma":"not_applicable","domain_scores_codex":[0.9992411,0.000083773804,0.00007039703,0.00022803112,0.00021780307,0.00015894699],"domain_scores_gemma":[0.9982515,0.00039292985,0.00012043666,0.00034925164,0.0006299306,0.00025596892],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00078723,0.0020832869,0.0013020092,0.0042577195,0.0012657039,0.0020614336,0.0026891988,0.0016585642,0.09225933],"category_scores_gemma":[0.005890572,0.0006675941,0.0013351446,0.008444941,0.00047913505,0.0010072404,0.0015678968,0.0012840366,0.058435794],"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":[0.00007554169,0.000016140484,0.0009285719,0.00062418496,0.000053121537,0.000027901717,0.00003351033,0.0006022258,0.00017513489,0.0006525389,0.99440986,0.0024012022],"study_design_scores_gemma":[0.00020160092,0.000012395736,0.0040511726,0.00026640855,0.00006536871,0.00004564137,0.000083860985,0.00080413785,0.00028652695,0.0013728383,0.99276954,0.00004047286],"about_ca_topic_score_codex":0.35819516,"about_ca_topic_score_gemma":0.5061212,"teacher_disagreement_score":0.35819516,"about_ca_system_score_codex":0.0031435245,"about_ca_system_score_gemma":0.007355962,"threshold_uncertainty_score":0.71222043},"labels":[],"label_agreement":null},{"id":"W6931064577","doi":"10.5281/zenodo.5116165","title":"D1.6 International Cooperation Strategy","year":2016,"lang":"en","type":"article","venue":"Zenodo (CERN European Organization for Nuclear Research)","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":0,"is_retracted":false,"has_abstract":true,"route_ca_aff":false,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":true,"ca_institutions":"","funders":"European Commission","keywords":"Alliance; European commission; Declaration; Commission; The arctic; White paper; Launched","score_opus":0.02369546661939615,"score_gpt":0.24508168185509804,"score_spread":0.2213862152357019,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W6931064577","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":[0.0020792363,0.003914111,0.012648298,0.039568186,0.007208399,0.0037336564,0.007157911,0.000891518,0.92279875],"genre_scores_gemma":[0.039208025,0.005322184,0.03830903,0.06134589,0.0015679421,0.010379231,0.020328201,0.0007940792,0.8227454],"study_design_codex":"not_applicable","study_design_gemma":"not_applicable","domain_scores_codex":[0.97263026,0.0077079036,0.0024601463,0.0022154108,0.008988549,0.0059977914],"domain_scores_gemma":[0.9776134,0.0021197312,0.0015413744,0.0024393478,0.01155871,0.004727404],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.027002623,0.0015984001,0.0010116281,0.0043639024,0.0034738798,0.013311,0.0035043976,0.012878372,0.04757779],"category_scores_gemma":[0.029479612,0.00080610014,0.0014191003,0.0036477747,0.0017760474,0.0049117547,0.011376765,0.007973091,0.047033347],"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":[0.00014140614,0.00012991189,0.00068869797,0.0006980176,0.000040617793,0.00030781698,0.00053820596,0.0006370706,0.0011042764,0.38266838,0.5603349,0.052710786],"study_design_scores_gemma":[0.000016465454,0.000023629173,0.00032013303,0.00016437535,0.0000039503525,0.00006776334,0.00012524829,0.00008541534,0.00011684339,0.0043773567,0.99468887,0.00000987098],"about_ca_topic_score_codex":0.01289906,"about_ca_topic_score_gemma":0.007233812,"teacher_disagreement_score":0.04757779,"about_ca_system_score_codex":0.008724637,"about_ca_system_score_gemma":0.055200156,"threshold_uncertainty_score":0.1591636},"labels":[],"label_agreement":null},{"id":"W6931358202","doi":"10.5281/zenodo.439971","title":"ga4gh/dockstore: 1.2.0-alpha.6","year":2017,"lang":"en","type":"other","venue":"Zenodo (CERN European Organization for Nuclear Research)","topic":"Genetic Syndromes and Imprinting","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":"Orthopaedic Innovation Centre","funders":"","keywords":"Component (thermodynamics); Relation (database); Work (physics); Set (abstract data type); Process (computing)","score_opus":0.022769126339747703,"score_gpt":0.24991136867366276,"score_spread":0.22714224233391506,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W6931358202","genre_codex":"software","genre_gemma":"software","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"software","genre_consensus":"software","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.0013778824,0.00021128234,0.08153372,0.00044294455,0.0003526533,0.00019776566,0.01593154,0.86987084,0.030081317],"genre_scores_gemma":[0.03200862,0.0005787364,0.07619173,0.0010005459,0.00022045223,0.00072326424,0.12416642,0.68297297,0.08213726],"study_design_codex":"not_applicable","study_design_gemma":"not_applicable","domain_scores_codex":[0.9979323,0.0002285174,0.00014244922,0.00044200654,0.00070076727,0.0005539076],"domain_scores_gemma":[0.99617565,0.0005070876,0.0001561234,0.001641942,0.00063428923,0.00088487135],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.002967643,0.003674682,0.002190264,0.002315689,0.0012627796,0.0056184647,0.012128897,0.0021036742,0.2197838],"category_scores_gemma":[0.008390619,0.0029226826,0.0020291584,0.0023965405,0.0013717879,0.0055331415,0.0068689804,0.0066491677,0.27165422],"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":[0.0006044222,0.00010438584,0.00052284286,0.00026946262,0.00007653451,0.00009117259,0.00009996109,0.0018838848,0.0028237663,0.008616282,0.9473673,0.03753991],"study_design_scores_gemma":[0.000651524,0.00007887325,0.0013477881,0.00017119228,0.0000769766,0.00027136027,0.00008586108,0.03726477,0.01922932,0.028347118,0.9122354,0.00023984852],"about_ca_topic_score_codex":0.0072099897,"about_ca_topic_score_gemma":0.0053985496,"teacher_disagreement_score":0.2197838,"about_ca_system_score_codex":0.002010194,"about_ca_system_score_gemma":0.0028193963,"threshold_uncertainty_score":0.73525006},"labels":[],"label_agreement":null},{"id":"W6931713377","doi":"10.5683/sp2/ofslnc","title":"Data from: Haploids adapt faster than diploids across a range of environments","year":2021,"lang":"en","type":"dataset","venue":"Borealis","topic":"Genetic Syndromes and Imprinting","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":"University of British Columbia","funders":"","keywords":"Ploidy; Range (aeronautics); Selection (genetic algorithm); Population; Adaptation (eye); Doubled haploidy","score_opus":0.032682732112443595,"score_gpt":0.2854356545845056,"score_spread":0.252752922472062,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W6931713377","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":[0.004227769,0.00036240346,0.00028269077,0.00017694368,0.000039890827,0.000018082334,0.99339676,0.00061748346,0.00087802316],"genre_scores_gemma":[0.0036293874,0.000075527736,0.00065142394,0.000054295888,0.0000056519584,0.00006743643,0.9950647,0.000051063987,0.00040052406],"study_design_codex":"not_applicable","study_design_gemma":"not_applicable","domain_scores_codex":[0.99840623,0.00036606583,0.00018971042,0.00050066813,0.0003710151,0.00016635665],"domain_scores_gemma":[0.99655354,0.0013350978,0.00037746484,0.0009229722,0.00053821475,0.00027278843],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.002104306,0.0020282916,0.0014068794,0.0025968691,0.0010828556,0.0019286253,0.0025639983,0.0018903923,0.014925378],"category_scores_gemma":[0.0074467515,0.0004828134,0.0011384289,0.0040136105,0.00053631497,0.00091534643,0.0015866486,0.0015325061,0.021188432],"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":[0.0006477527,0.0001933235,0.023039902,0.003385207,0.00056788354,0.00026291065,0.00016559349,0.0062196506,0.0017700572,0.0013125015,0.94844294,0.013992215],"study_design_scores_gemma":[0.0012436577,0.00012443653,0.069118306,0.0004921787,0.0002511904,0.0004892779,0.00027981668,0.0060717976,0.003440357,0.00303226,0.91530895,0.00014784576],"about_ca_topic_score_codex":0.015233321,"about_ca_topic_score_gemma":0.03147791,"teacher_disagreement_score":0.015233321,"about_ca_system_score_codex":0.0011055524,"about_ca_system_score_gemma":0.0012726634,"threshold_uncertainty_score":0.049930394},"labels":[],"label_agreement":null},{"id":"W6931780144","doi":"10.5683/sp2/4wynm9","title":"Using Light Detection and Ranging (LiDAR) and Google Earth imagery to identify whether ponds are connected to stable ground water inputs","year":2021,"lang":"en","type":"dataset","venue":"Borealis","topic":"Genetic Syndromes and Imprinting","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":true,"ca_institutions":"University of British Columbia","funders":"","keywords":"Threatened species; Groundwater; Hydrology (agriculture); Terrain; Water table; Topographic Wetness Index; Resilience (materials science); Vegetation (pathology); Surface water","score_opus":0.014771187722420072,"score_gpt":0.2660982649202878,"score_spread":0.25132707719786773,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W6931780144","genre_codex":"empirical","genre_gemma":"dataset","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"dataset","genre_consensus":null,"domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9927482,0.000042680786,0.0023733391,0.000035485064,0.000003814541,0.000061438885,0.0011549668,0.00014849413,0.0034316913],"genre_scores_gemma":[0.99251807,0.000059926366,0.0055852993,0.000010624866,0.0000013318315,0.000016761936,0.0012285996,0.000005327367,0.00057402713],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.999739,0.000033353477,0.000018567636,0.00004642686,0.00010192449,0.000060701444],"domain_scores_gemma":[0.99970007,0.000055731,0.00008063816,0.00003259717,0.00009256581,0.000038339207],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00024254505,0.0001831665,0.0001261324,0.0023158763,0.00029285668,0.00066435995,0.00018985603,0.00019075077,0.0009892965],"category_scores_gemma":[0.0008364541,0.000109902656,0.00023189682,0.0019059152,0.00021321114,0.000570194,0.00066003564,0.0001476007,0.00031341112],"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":[0.00012210387,0.00007426549,0.88621444,0.00012587647,0.00007406356,0.0006298798,0.0015266851,0.0038580825,0.009437361,0.0003183237,0.0014390049,0.09617991],"study_design_scores_gemma":[0.0000086772,0.00009107891,0.9620247,0.000046849702,0.000045533354,0.0003174649,0.005477074,0.02618128,0.0026989176,0.00034277822,0.0027421385,0.000023451687],"about_ca_topic_score_codex":0.02957493,"about_ca_topic_score_gemma":0.09047706,"teacher_disagreement_score":0.02957493,"about_ca_system_score_codex":0.00032538432,"about_ca_system_score_gemma":0.00041569167,"threshold_uncertainty_score":0.058805585},"labels":[],"label_agreement":null},{"id":"W6931862107","doi":"10.5683/sp2/jojyop","title":"Coexpression Analysis of Human Genes Across Many Microarray Data Sets","year":2019,"lang":"en","type":"dataset","venue":"Borealis","topic":"Genetic Syndromes and Imprinting","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":"Columbia College; Genome British Columbia","funders":"","keywords":"Microarray analysis techniques; Gene; Microarray; Gene expression profiling; Gene expression; Gene regulatory network; Expression (computer science); DNA microarray","score_opus":0.036466880075834616,"score_gpt":0.34118089168534155,"score_spread":0.30471401160950695,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W6931862107","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":[0.14787313,0.0028003256,0.0069372472,0.00040459394,0.00008319331,0.00011438252,0.8377724,0.0014771527,0.0025374186],"genre_scores_gemma":[0.076534964,0.00048473154,0.0071342066,0.00013343904,0.000022978065,0.00023326665,0.914638,0.00008516748,0.0007333124],"study_design_codex":"not_applicable","study_design_gemma":"not_applicable","domain_scores_codex":[0.9983719,0.0003388805,0.00018262655,0.00060954876,0.00037548534,0.00012168823],"domain_scores_gemma":[0.9977361,0.0012290428,0.00021498647,0.00044985293,0.00024832165,0.00012159693],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0015379853,0.0013032157,0.0012455982,0.0029517948,0.00062763627,0.0009766226,0.0011614298,0.0009166429,0.0028531922],"category_scores_gemma":[0.0046716966,0.00032413568,0.00088455033,0.0050739553,0.00038792202,0.00037507477,0.0011541492,0.0007767333,0.0021547761],"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":[0.0039265687,0.0009496657,0.28549826,0.00835376,0.0042216284,0.005285872,0.00083740277,0.037698932,0.07186306,0.005375889,0.40700498,0.16898406],"study_design_scores_gemma":[0.0010589769,0.000589751,0.5836576,0.00034646798,0.0012350227,0.0044024317,0.000616733,0.03437316,0.032314073,0.0070737423,0.33409193,0.00024007467],"about_ca_topic_score_codex":0.0066628535,"about_ca_topic_score_gemma":0.010135376,"teacher_disagreement_score":0.0066628535,"about_ca_system_score_codex":0.00066762423,"about_ca_system_score_gemma":0.0008488319,"threshold_uncertainty_score":0.013248146},"labels":[],"label_agreement":null},{"id":"W6939420541","doi":"10.6084/m9.figshare.20064362","title":"Additional file 6 of Gain and loss of TASK3 channel function and its regulation by novel variation cause KCNK9 imprinting syndrome","year":2022,"lang":"en","type":"article","venue":"Figshare","topic":"Genetic Syndromes and Imprinting","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":"BC Children's Hospital","funders":"","keywords":"Channel (broadcasting); Selectivity; Gene; Function (biology); HEK 293 cells; Cell; Genomic imprinting; Filter (signal processing); Mutation","score_opus":0.013462243930767316,"score_gpt":0.2027190654999588,"score_spread":0.1892568215691915,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W6939420541","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":[0.0004890218,0.000028281509,0.00054761756,0.0001554159,0.0000720276,0.00010706922,0.9968413,0.00054670573,0.0012126963],"genre_scores_gemma":[0.018486092,0.00026735384,0.00640985,0.0009958744,0.00020573131,0.001438965,0.95578027,0.0018010682,0.014614902],"study_design_codex":"not_applicable","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99923635,0.00009628136,0.00013743521,0.00019525435,0.00019394635,0.00014068525],"domain_scores_gemma":[0.986139,0.010390592,0.0007808127,0.0010067353,0.0010579235,0.0006250243],"candidate_categories":["insufficient_payload"],"consensus_categories":[],"category_scores_codex":[0.0013327992,0.0013049135,0.0018205668,0.0021720435,0.001294378,0.0015902596,0.002504166,0.0018720975,0.8861678],"category_scores_gemma":[0.01868334,0.00077664555,0.0012292074,0.0028719953,0.00040573135,0.0015678321,0.0010851548,0.0011210792,0.16209029],"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":[0.0008159483,0.00023995609,0.0052610743,0.0035772999,0.000114554896,0.00077738217,0.00015179343,0.0006933273,0.0008975621,0.0011900896,0.97070765,0.015573316],"study_design_scores_gemma":[0.0112367505,0.0008125395,0.07506702,0.0050363173,0.00043636494,0.0049268184,0.00076394633,0.0032565105,0.004372335,0.01950872,0.87418616,0.00039651064],"about_ca_topic_score_codex":0.008350091,"about_ca_topic_score_gemma":0.010474843,"teacher_disagreement_score":0.8861678,"about_ca_system_score_codex":0.001050656,"about_ca_system_score_gemma":0.0015323019,"threshold_uncertainty_score":0.16236776},"labels":[],"label_agreement":null},{"id":"W6939728741","doi":"10.6084/m9.figshare.20064371.v1","title":"Additional file 9 of Gain and loss of TASK3 channel function and its regulation by novel variation cause KCNK9 imprinting syndrome","year":2022,"lang":"en","type":"article","venue":"Figshare","topic":"Genetic Syndromes and Imprinting","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":"BC Children's Hospital","funders":"","keywords":"Function (biology); Loss function; Channel (broadcasting); Gene; HEK 293 cells; Variation (astronomy); Mutation","score_opus":0.013477445620077237,"score_gpt":0.20279957040024266,"score_spread":0.1893221247801654,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W6939728741","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":[0.0002988206,0.000027870292,0.00021081616,0.00012496306,0.00003171788,0.0000546773,0.99824893,0.0002193262,0.0007828401],"genre_scores_gemma":[0.016723806,0.00028415764,0.0032018477,0.00096037105,0.0002037087,0.0012108396,0.96374345,0.00092594157,0.012745846],"study_design_codex":"not_applicable","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9991873,0.00012086971,0.0001694413,0.0002118392,0.00019407559,0.00011643975],"domain_scores_gemma":[0.97819406,0.016888142,0.0014045394,0.0011198686,0.0017852961,0.00060808985],"candidate_categories":["insufficient_payload"],"consensus_categories":[],"category_scores_codex":[0.0012432892,0.0010631512,0.001477053,0.0021385755,0.00093532074,0.0014674537,0.001859516,0.0014036696,0.870145],"category_scores_gemma":[0.027070219,0.0005703157,0.001134918,0.0029688287,0.00031243556,0.0014193051,0.0009370431,0.0008529998,0.14028764],"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":[0.00064307614,0.00012407776,0.0055787484,0.0029998424,0.000106617386,0.00034178214,0.00009547883,0.00044222473,0.00033888363,0.00072355976,0.97664887,0.011956865],"study_design_scores_gemma":[0.010766041,0.0006387605,0.09453553,0.006913752,0.0006111704,0.0032589168,0.000799166,0.0021435951,0.0023380946,0.019105714,0.8585444,0.00034486997],"about_ca_topic_score_codex":0.008066981,"about_ca_topic_score_gemma":0.0112766065,"teacher_disagreement_score":0.870145,"about_ca_system_score_codex":0.00090538396,"about_ca_system_score_gemma":0.001305639,"threshold_uncertainty_score":0.18522239},"labels":[],"label_agreement":null},{"id":"W6939841432","doi":"10.6084/m9.figshare.26986399.v1","title":"Additional file 1 of Conservation and divergence of canonical and non-canonical imprinting in murids","year":2024,"lang":"en","type":"article","venue":"Figshare","topic":"Genetic Syndromes and Imprinting","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":"BC Children's Hospital; University of British Columbia","funders":"","keywords":"Imprinting (psychology); Divergence (linguistics); Entropy (arrow of time); Genome","score_opus":0.012503434411400817,"score_gpt":0.23530005347426144,"score_spread":0.22279661906286063,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W6939841432","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":[0.00019643441,0.0000194448,0.00025083742,0.000049315953,0.000023044327,0.00002080609,0.99801564,0.00031364814,0.0011109087],"genre_scores_gemma":[0.00746966,0.00015716649,0.0033486893,0.00025108788,0.00006651682,0.00043104895,0.9789853,0.0012341271,0.008056281],"study_design_codex":"not_applicable","study_design_gemma":"not_applicable","domain_scores_codex":[0.9994246,0.00008647945,0.0000686722,0.0001679368,0.00016213644,0.00009023933],"domain_scores_gemma":[0.98693347,0.00977632,0.0006459563,0.0008610201,0.0013808435,0.00040240827],"candidate_categories":["insufficient_payload"],"consensus_categories":[],"category_scores_codex":[0.0012110798,0.0009584726,0.0012026723,0.0029944626,0.0011732354,0.0015552953,0.0018794144,0.0010190872,0.8735932],"category_scores_gemma":[0.015687738,0.00055991905,0.00072796614,0.0052188532,0.00033210838,0.0016783695,0.0010232169,0.00090722594,0.2548374],"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":[0.0001837932,0.00005740006,0.0026474653,0.0018939999,0.000039487786,0.00007235152,0.00009529975,0.00039186864,0.00033940646,0.0010427504,0.9842107,0.009025507],"study_design_scores_gemma":[0.0016385816,0.00016960296,0.03443063,0.0019838705,0.00014850112,0.0006695376,0.0004246258,0.0013218025,0.0011852969,0.009817146,0.94807893,0.0001315381],"about_ca_topic_score_codex":0.0068303957,"about_ca_topic_score_gemma":0.011106966,"teacher_disagreement_score":0.8735932,"about_ca_system_score_codex":0.001005254,"about_ca_system_score_gemma":0.0013296993,"threshold_uncertainty_score":0.18030387},"labels":[],"label_agreement":null},{"id":"W6957852115","doi":"10.6084/m9.figshare.20064368","title":"Additional file 8 of Gain and loss of TASK3 channel function and its regulation by novel variation cause KCNK9 imprinting syndrome","year":2022,"lang":"en","type":"article","venue":"Figshare","topic":"Genetic Syndromes and Imprinting","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":"BC Children's Hospital","funders":"","keywords":"Function (biology); Extracellular; Channel (broadcasting); Loss function; HEK 293 cells; Gene; Variation (astronomy)","score_opus":0.013470722356893429,"score_gpt":0.2027671882946675,"score_spread":0.18929646593777408,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W6957852115","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":[0.00036332,0.000035474382,0.0002752616,0.00014654978,0.000043499906,0.00007091538,0.997979,0.0002504331,0.0008355344],"genre_scores_gemma":[0.020840263,0.00036225616,0.004198952,0.0011445116,0.00027760898,0.0016548019,0.95555425,0.0011390274,0.014828267],"study_design_codex":"not_applicable","study_design_gemma":"not_applicable","domain_scores_codex":[0.99916494,0.0001243203,0.00017734594,0.000215052,0.00019668615,0.00012175238],"domain_scores_gemma":[0.977417,0.017567877,0.001398427,0.0011764026,0.0018571644,0.00058314204],"candidate_categories":["insufficient_payload"],"consensus_categories":[],"category_scores_codex":[0.0013326039,0.0011378472,0.001593683,0.0021730133,0.00095820596,0.0015476326,0.0021133067,0.0015366019,0.8684674],"category_scores_gemma":[0.029724455,0.00063323765,0.0012408758,0.0030974138,0.00033197133,0.0014597026,0.0008990532,0.00090818154,0.1335],"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":[0.00078693446,0.00013584016,0.006121998,0.003943893,0.00013004028,0.00041578023,0.00011048277,0.0005337632,0.00039172603,0.0007595644,0.97346115,0.013208877],"study_design_scores_gemma":[0.013930187,0.00075411494,0.10398772,0.00824878,0.00079299405,0.003639277,0.00084942894,0.0026521184,0.0025471812,0.020528372,0.8416834,0.0003865174],"about_ca_topic_score_codex":0.008035134,"about_ca_topic_score_gemma":0.011307563,"teacher_disagreement_score":0.8684674,"about_ca_system_score_codex":0.0008972432,"about_ca_system_score_gemma":0.001331431,"threshold_uncertainty_score":0.18761533},"labels":[],"label_agreement":null},{"id":"W6957913438","doi":"10.60692/zzd1c-pvz77","title":"Craniofacial anthropometric measurements of the cohort of Egyptian male school children and their utility in detection of abnormalities","year":2024,"lang":"en","type":"article","venue":"Greater South Information System","topic":"Genetic Syndromes and Imprinting","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":"Polytechnique Montréal","funders":"","keywords":"Craniofacial; Anthropometry; Cohort; Craniofacial abnormality; Nose; Body height; Epidemiology","score_opus":0.017783148243118496,"score_gpt":0.20723936109702287,"score_spread":0.18945621285390438,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W6957913438","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99949896,0.00006439668,0.00004574612,0.000011087096,0.0000015288239,0.0000045211973,0.00017308816,0.0000021307837,0.00019853971],"genre_scores_gemma":[0.9993926,0.000070888964,0.00015244525,0.00000675697,0.0000024939256,0.000009513392,0.00021409226,0.0000011518545,0.00015004489],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9997055,0.00005095361,0.000043034117,0.00007048497,0.000084718,0.000045232035],"domain_scores_gemma":[0.9994937,0.0000641144,0.00022670499,0.000041958327,0.00011079265,0.00006263158],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00042850038,0.00029903874,0.00019882982,0.0011555364,0.0003214828,0.00042265592,0.00022524512,0.00024042912,0.0013361005],"category_scores_gemma":[0.0011246123,0.00018095199,0.00024340732,0.0005793554,0.00026667357,0.00022496565,0.00035469187,0.00027531324,0.00018810332],"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":[0.000028519931,0.00001317855,0.99776936,0.0000045400525,0.000010619197,0.00007019614,0.000079435835,0.000014386995,0.00043546077,0.000008188142,0.00003291737,0.0015331362],"study_design_scores_gemma":[4.2999025e-7,0.000021270354,0.9996117,0.0000013021324,0.0000033710576,0.00010821125,0.00013012784,0.00002019732,0.00006440517,0.0000019113656,0.00003641166,6.8218304e-7],"about_ca_topic_score_codex":0.0065059313,"about_ca_topic_score_gemma":0.007192221,"teacher_disagreement_score":0.0065059313,"about_ca_system_score_codex":0.0002639289,"about_ca_system_score_gemma":0.00025284255,"threshold_uncertainty_score":0.012936115},"labels":[],"label_agreement":null},{"id":"W6958412846","doi":"10.6084/m9.figshare.20064359.v1","title":"Additional file 5 of Gain and loss of TASK3 channel function and its regulation by novel variation cause KCNK9 imprinting syndrome","year":2022,"lang":"en","type":"article","venue":"Figshare","topic":"Genetic Syndromes and Imprinting","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":"BC Children's Hospital","funders":"","keywords":"Loss function; Function (biology); Channel (broadcasting); Variation (astronomy); Gene; Imprinting (psychology)","score_opus":0.013466912802269063,"score_gpt":0.20276054185243894,"score_spread":0.1892936290501699,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W6958412846","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":[0.00034968826,0.00003635546,0.0002889886,0.00014875023,0.000034845667,0.00006694705,0.9979175,0.00022244651,0.00093446317],"genre_scores_gemma":[0.022323651,0.00037333797,0.0043963296,0.001284267,0.00023976625,0.0013974904,0.95563465,0.000964737,0.0133858295],"study_design_codex":"not_applicable","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9992756,0.00011068568,0.0001549139,0.00019180737,0.00016029911,0.00010664759],"domain_scores_gemma":[0.97625595,0.018990394,0.0014149836,0.0010743081,0.0016800117,0.00058441184],"candidate_categories":["insufficient_payload"],"consensus_categories":[],"category_scores_codex":[0.001230002,0.0010942703,0.0014373345,0.002121395,0.0010082364,0.0015179073,0.0018761543,0.0015559314,0.8649833],"category_scores_gemma":[0.026502473,0.0005976708,0.001190787,0.0028225994,0.000331496,0.0014663943,0.0008707805,0.0009209613,0.11180054],"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":[0.00071823044,0.00014044538,0.006735675,0.0041435403,0.00012949963,0.00049525086,0.00013159757,0.00063733687,0.00038352062,0.0009768739,0.9705091,0.01499906],"study_design_scores_gemma":[0.012379597,0.00068808306,0.10986433,0.009589943,0.0007964293,0.0045683454,0.0008694619,0.0028679548,0.0025771724,0.02342118,0.83198583,0.00039165787],"about_ca_topic_score_codex":0.009536082,"about_ca_topic_score_gemma":0.012933396,"teacher_disagreement_score":0.8649833,"about_ca_system_score_codex":0.00094562623,"about_ca_system_score_gemma":0.0013498443,"threshold_uncertainty_score":0.19258481},"labels":[],"label_agreement":null},{"id":"W6958421332","doi":"10.6084/m9.figshare.20064359","title":"Additional file 5 of Gain and loss of TASK3 channel function and its regulation by novel variation cause KCNK9 imprinting syndrome","year":2022,"lang":"en","type":"article","venue":"Figshare","topic":"Genetic Syndromes and Imprinting","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":"BC Children's Hospital","funders":"","keywords":"Loss function; Function (biology); Channel (broadcasting); Variation (astronomy); Gene; Imprinting (psychology)","score_opus":0.013466912802269063,"score_gpt":0.20276054185243894,"score_spread":0.1892936290501699,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W6958421332","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":[0.00034968826,0.00003635546,0.0002889886,0.00014875023,0.000034845667,0.00006694705,0.9979175,0.00022244651,0.00093446317],"genre_scores_gemma":[0.022323651,0.00037333797,0.0043963296,0.001284267,0.00023976625,0.0013974904,0.95563465,0.000964737,0.0133858295],"study_design_codex":"not_applicable","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9992756,0.00011068568,0.0001549139,0.00019180737,0.00016029911,0.00010664759],"domain_scores_gemma":[0.97625595,0.018990394,0.0014149836,0.0010743081,0.0016800117,0.00058441184],"candidate_categories":["insufficient_payload"],"consensus_categories":[],"category_scores_codex":[0.001230002,0.0010942703,0.0014373345,0.002121395,0.0010082364,0.0015179073,0.0018761543,0.0015559314,0.8649833],"category_scores_gemma":[0.026502473,0.0005976708,0.001190787,0.0028225994,0.000331496,0.0014663943,0.0008707805,0.0009209613,0.11180054],"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":[0.00071823044,0.00014044538,0.006735675,0.0041435403,0.00012949963,0.00049525086,0.00013159757,0.00063733687,0.00038352062,0.0009768739,0.9705091,0.01499906],"study_design_scores_gemma":[0.012379597,0.00068808306,0.10986433,0.009589943,0.0007964293,0.0045683454,0.0008694619,0.0028679548,0.0025771724,0.02342118,0.83198583,0.00039165787],"about_ca_topic_score_codex":0.009536082,"about_ca_topic_score_gemma":0.012933396,"teacher_disagreement_score":0.8649833,"about_ca_system_score_codex":0.00094562623,"about_ca_system_score_gemma":0.0013498443,"threshold_uncertainty_score":0.19258481},"labels":[],"label_agreement":null},{"id":"W6958549180","doi":"10.6084/m9.figshare.26630146.v1","title":"Additional file 1 of Safety and efficacy of pegunigalsidase alfa in patients with Fabry disease who were previously treated with agalsidase alfa: results from BRIDGE, a phase 3 open-label study","year":2024,"lang":"en","type":"article","venue":"Figshare","topic":"Genetic Syndromes and Imprinting","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":"Dalhousie University","funders":"","keywords":"Fabry disease; Selection (genetic algorithm); Enzyme replacement therapy; Clinical trial; Disease","score_opus":0.017343677665007842,"score_gpt":0.2640277896681375,"score_spread":0.24668411200312967,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W6958549180","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":[0.0009418907,0.000105014784,0.00038964645,0.0003278889,0.00004121032,0.0008605297,0.9944243,0.0002291388,0.002680413],"genre_scores_gemma":[0.048385542,0.0008018499,0.009615576,0.0025464077,0.00044377224,0.019583017,0.8887033,0.00057778216,0.02934276],"study_design_codex":"not_applicable","study_design_gemma":"not_applicable","domain_scores_codex":[0.9992341,0.00021538297,0.00018901554,0.00012334043,0.00014870433,0.00008955187],"domain_scores_gemma":[0.9771049,0.01666383,0.0027326266,0.0009777875,0.0020365631,0.00048434286],"candidate_categories":["insufficient_payload"],"consensus_categories":[],"category_scores_codex":[0.0024278841,0.0009211725,0.001542874,0.0009953898,0.0005907194,0.0010391081,0.0011755,0.0010480065,0.800931],"category_scores_gemma":[0.024628868,0.0004883117,0.0010104587,0.0017963466,0.00020615713,0.0012840446,0.00049023714,0.00089666963,0.074562944],"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":[0.008252878,0.0005852724,0.0025354566,0.008503742,0.0003170716,0.00012191344,0.000054660453,0.00079006125,0.00023784507,0.0012926765,0.9466006,0.030707888],"study_design_scores_gemma":[0.1525907,0.006101546,0.0562789,0.011556697,0.001598262,0.0015219449,0.00023338501,0.004437039,0.0026597735,0.016370347,0.7463932,0.00025818625],"about_ca_topic_score_codex":0.0022439214,"about_ca_topic_score_gemma":0.004646305,"teacher_disagreement_score":0.800931,"about_ca_system_score_codex":0.001063015,"about_ca_system_score_gemma":0.0016608253,"threshold_uncertainty_score":0.2839477},"labels":[],"label_agreement":null},{"id":"W6968859774","doi":"10.5281/zenodo.4651578","title":"Supplementary Figures","year":2021,"lang":"en","type":"other","venue":"Zenodo (CERN European Organization for Nuclear Research)","topic":"Genetic Syndromes and Imprinting","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":"University of Guelph","funders":"","keywords":"Venn diagram; Intersection (aeronautics); Diagram; Network analysis; Social network analysis; Gene","score_opus":0.020402151944611393,"score_gpt":0.24610364579427374,"score_spread":0.22570149384966234,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W6968859774","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":[0.00096482533,0.0022820923,0.016645957,0.002390023,0.007980036,0.00043312428,0.8451135,0.010874361,0.11331604],"genre_scores_gemma":[0.006846004,0.0027109298,0.019827044,0.0037602573,0.0014416964,0.0012135464,0.7934355,0.007405028,0.16335988],"study_design_codex":"not_applicable","study_design_gemma":"not_applicable","domain_scores_codex":[0.9980704,0.00027620827,0.00015454316,0.00049104093,0.00085140637,0.00015642944],"domain_scores_gemma":[0.9941963,0.0018237954,0.00036016037,0.0008359002,0.0021998656,0.0005838747],"candidate_categories":["insufficient_payload"],"consensus_categories":[],"category_scores_codex":[0.0021192178,0.0016186213,0.0013427896,0.0036181149,0.0025283368,0.004308602,0.0025775137,0.0022167524,0.8089672],"category_scores_gemma":[0.011552442,0.00092656,0.0014767086,0.0043506427,0.00053821254,0.0025530122,0.0017312518,0.0022679532,0.49394846],"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":[0.00006266399,0.000023561268,0.00023667373,0.00055576896,0.000019760002,0.00006872048,0.000024185538,0.00029112006,0.00042788303,0.002664623,0.9795379,0.016087191],"study_design_scores_gemma":[0.000047077436,0.000016964581,0.0006908762,0.00019644691,0.000016468217,0.00015502499,0.000033106568,0.00021518717,0.00045133932,0.0038969675,0.9942601,0.000020508125],"about_ca_topic_score_codex":0.006313509,"about_ca_topic_score_gemma":0.011006359,"teacher_disagreement_score":0.8089672,"about_ca_system_score_codex":0.0023485213,"about_ca_system_score_gemma":0.0030787138,"threshold_uncertainty_score":0.27248514},"labels":[],"label_agreement":null},{"id":"W6977119697","doi":"10.6084/m9.figshare.26986429.v1","title":"Additional file 10 of Conservation and divergence of canonical and non-canonical imprinting in murids","year":2024,"lang":"en","type":"article","venue":"Figshare","topic":"Genetic Syndromes and Imprinting","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":"BC Children's Hospital; University of British Columbia","funders":"","keywords":"Imprinting (psychology); Divergence (linguistics); Entropy (arrow of time); Genome","score_opus":0.013896958573758356,"score_gpt":0.2409133182193833,"score_spread":0.22701635964562494,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W6977119697","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":[0.00009826995,0.00023303382,0.00027976758,0.0003404332,0.00015037,0.00004716793,0.9952976,0.0004168238,0.0031365578],"genre_scores_gemma":[0.008341538,0.0015774881,0.0036394838,0.001389151,0.0005094426,0.0009875275,0.946382,0.0018617779,0.035311554],"study_design_codex":"not_applicable","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9991007,0.00019155115,0.00013291309,0.00021458481,0.00026110027,0.00009925818],"domain_scores_gemma":[0.97554463,0.018168097,0.001240805,0.0012914038,0.0030971812,0.0006578796],"candidate_categories":["insufficient_payload"],"consensus_categories":[],"category_scores_codex":[0.0021007054,0.0007914229,0.0014525461,0.0040774834,0.0008474668,0.0018629753,0.0019333056,0.0012264252,0.9006961],"category_scores_gemma":[0.031019615,0.0005366236,0.0008741882,0.005935468,0.00033690574,0.0025125006,0.0012345038,0.0008869857,0.27457994],"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":[0.00007750271,0.000009508304,0.00049057713,0.002428878,0.00002020397,0.00003684587,0.000042371492,0.000093919516,0.00005306331,0.0007257973,0.98876065,0.007260681],"study_design_scores_gemma":[0.0004251272,0.00003970067,0.0074444264,0.0027181464,0.000070809205,0.00025058645,0.0001318517,0.00015781034,0.00017941016,0.0042377478,0.98429316,0.000051068924],"about_ca_topic_score_codex":0.0066773486,"about_ca_topic_score_gemma":0.00923858,"teacher_disagreement_score":0.9006961,"about_ca_system_score_codex":0.0013634837,"about_ca_system_score_gemma":0.0019275711,"threshold_uncertainty_score":0.14164495},"labels":[],"label_agreement":null},{"id":"W6977166992","doi":"10.6084/m9.figshare.28040104","title":"Additional file 1 of Cognitive benefits of folic acid supplementation during pregnancy track with epigenetic changes at an imprint regulator","year":2024,"lang":"en","type":"article","venue":"Figshare","topic":"Genetic Syndromes and Imprinting","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":"University of British Columbia","funders":"","keywords":"Regulator; Epigenetics; EPIC; CpG site; Table (database); Offspring; Pregnancy; Folic acid; DNA methylation","score_opus":0.017674961586394373,"score_gpt":0.24242228909963967,"score_spread":0.2247473275132453,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W6977166992","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":[0.00021977481,0.00003754844,0.00036905264,0.00008422247,0.000028277525,0.00013471502,0.99811816,0.00021204221,0.0007962131],"genre_scores_gemma":[0.014085659,0.00045596773,0.008923946,0.0010647578,0.00017189531,0.0067912014,0.94719285,0.001298073,0.020015616],"study_design_codex":"not_applicable","study_design_gemma":"observational","domain_scores_codex":[0.9993579,0.00013916343,0.0001022411,0.0001672714,0.00015251675,0.000081002414],"domain_scores_gemma":[0.9816742,0.014804111,0.00081578793,0.00089475187,0.0014126019,0.000398562],"candidate_categories":["insufficient_payload"],"consensus_categories":[],"category_scores_codex":[0.0015667628,0.0012528021,0.0015825235,0.0015516438,0.00097373023,0.0014900855,0.0018443887,0.0012782874,0.9023862],"category_scores_gemma":[0.02471221,0.00057147007,0.0010457843,0.002465941,0.00026091727,0.0013229147,0.0008139687,0.0009030828,0.16463546],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0012369438,0.00023585277,0.0027062476,0.0069238422,0.000119775046,0.00012206428,0.000102168415,0.00050068024,0.0003188219,0.00082269567,0.96487904,0.02203196],"study_design_scores_gemma":[0.015087956,0.0014573354,0.045894053,0.008697705,0.000769516,0.001323987,0.00068666885,0.0026714797,0.0026390005,0.018885043,0.90158594,0.00030141117],"about_ca_topic_score_codex":0.0064756577,"about_ca_topic_score_gemma":0.011125669,"teacher_disagreement_score":0.9023862,"about_ca_system_score_codex":0.0010029227,"about_ca_system_score_gemma":0.0017484025,"threshold_uncertainty_score":0.13923419},"labels":[],"label_agreement":null},{"id":"W6977240968","doi":"10.6084/m9.figshare.20064362.v1","title":"Additional file 6 of Gain and loss of TASK3 channel function and its regulation by novel variation cause KCNK9 imprinting syndrome","year":2022,"lang":"en","type":"article","venue":"Figshare","topic":"Genetic Syndromes and Imprinting","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":"BC Children's Hospital","funders":"","keywords":"Channel (broadcasting); Selectivity; Gene; Function (biology); HEK 293 cells; Cell; Genomic imprinting; Filter (signal processing); Mutation","score_opus":0.013462243930767316,"score_gpt":0.2027190654999588,"score_spread":0.1892568215691915,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W6977240968","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":[0.0004890218,0.000028281509,0.00054761756,0.0001554159,0.0000720276,0.00010706922,0.9968413,0.00054670573,0.0012126963],"genre_scores_gemma":[0.018486092,0.00026735384,0.00640985,0.0009958744,0.00020573131,0.001438965,0.95578027,0.0018010682,0.014614902],"study_design_codex":"not_applicable","study_design_gemma":"not_applicable","domain_scores_codex":[0.99923635,0.00009628136,0.00013743521,0.00019525435,0.00019394635,0.00014068525],"domain_scores_gemma":[0.986139,0.010390592,0.0007808127,0.0010067353,0.0010579235,0.0006250243],"candidate_categories":["insufficient_payload"],"consensus_categories":[],"category_scores_codex":[0.0013327992,0.0013049135,0.0018205668,0.0021720435,0.001294378,0.0015902596,0.002504166,0.0018720975,0.8861678],"category_scores_gemma":[0.01868334,0.00077664555,0.0012292074,0.0028719953,0.00040573135,0.0015678321,0.0010851548,0.0011210792,0.16209029],"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":[0.0008159483,0.00023995609,0.0052610743,0.0035772999,0.000114554896,0.00077738217,0.00015179343,0.0006933273,0.0008975621,0.0011900896,0.97070765,0.015573316],"study_design_scores_gemma":[0.0112367505,0.0008125395,0.07506702,0.0050363173,0.00043636494,0.0049268184,0.00076394633,0.0032565105,0.004372335,0.01950872,0.87418616,0.00039651064],"about_ca_topic_score_codex":0.008350091,"about_ca_topic_score_gemma":0.010474843,"teacher_disagreement_score":0.8861678,"about_ca_system_score_codex":0.001050656,"about_ca_system_score_gemma":0.0015323019,"threshold_uncertainty_score":0.16236776},"labels":[],"label_agreement":null},{"id":"W6977277581","doi":"10.6084/m9.figshare.12875880","title":"Additional file 4 of The testosterone-dependent and independent transcriptional networks in the hypothalamus of Gpr54 and Kiss1 knockout male mice are not fully equivalent","year":2020,"lang":"en","type":"article","venue":"Figshare","topic":"Genetic Syndromes and Imprinting","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":"Vancouver Coastal Health Research Institute; University of British Columbia; BC Cancer Agency","funders":"Biotechnology and Biological Sciences Research Council","keywords":"Transcription (linguistics); Hypothalamus; Transcription factor; Knockout mouse; Set (abstract data type); Gene","score_opus":0.026509787740033253,"score_gpt":0.20900716677144707,"score_spread":0.1824973790314138,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W6977277581","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":[0.00024236452,0.000027146321,0.0007402215,0.0000922838,0.000056956585,0.000033922483,0.9960918,0.001565264,0.0011500161],"genre_scores_gemma":[0.008868197,0.00018356027,0.0069235233,0.000583352,0.00011221232,0.00082294963,0.9666245,0.004529721,0.011352022],"study_design_codex":"not_applicable","study_design_gemma":"not_applicable","domain_scores_codex":[0.99949956,0.000053289146,0.00005095546,0.00013595367,0.00015881445,0.00010134022],"domain_scores_gemma":[0.9931177,0.0048138015,0.00034253421,0.00053865486,0.00086713367,0.00032023908],"candidate_categories":["insufficient_payload"],"consensus_categories":[],"category_scores_codex":[0.0009059747,0.0012845583,0.0017321339,0.001947048,0.0011702692,0.0017010488,0.0020946118,0.001274693,0.8873271],"category_scores_gemma":[0.007578467,0.00086604286,0.0012672818,0.0027963347,0.0003750857,0.0017154205,0.0011037093,0.0013507812,0.2557295],"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":[0.00042428993,0.00009627763,0.0018842815,0.0020653647,0.000055471068,0.00014596044,0.0000861556,0.00044980677,0.0012261744,0.00087209634,0.9840847,0.008609384],"study_design_scores_gemma":[0.004625953,0.00038774888,0.041760806,0.0023754232,0.00027208633,0.0012337121,0.00047636768,0.003009687,0.0072992234,0.016135164,0.92213583,0.00028799198],"about_ca_topic_score_codex":0.0069574444,"about_ca_topic_score_gemma":0.011450258,"teacher_disagreement_score":0.8873271,"about_ca_system_score_codex":0.0010730957,"about_ca_system_score_gemma":0.0013447183,"threshold_uncertainty_score":0.16071415},"labels":[],"label_agreement":null},{"id":"W6977385879","doi":"10.6084/m9.figshare.12875880.v1","title":"Additional file 4 of The testosterone-dependent and independent transcriptional networks in the hypothalamus of Gpr54 and Kiss1 knockout male mice are not fully equivalent","year":2020,"lang":"en","type":"article","venue":"Figshare","topic":"Genetic Syndromes and Imprinting","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":"Vancouver Coastal Health Research Institute; University of British Columbia; BC Cancer Agency","funders":"","keywords":"Transcription (linguistics); Hypothalamus; Transcription factor; Knockout mouse; Set (abstract data type); Gene","score_opus":0.026509787740033253,"score_gpt":0.20900716677144707,"score_spread":0.1824973790314138,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W6977385879","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":[0.00024236452,0.000027146321,0.0007402215,0.0000922838,0.000056956585,0.000033922483,0.9960918,0.001565264,0.0011500161],"genre_scores_gemma":[0.008868197,0.00018356027,0.0069235233,0.000583352,0.00011221232,0.00082294963,0.9666245,0.004529721,0.011352022],"study_design_codex":"not_applicable","study_design_gemma":"not_applicable","domain_scores_codex":[0.99949956,0.000053289146,0.00005095546,0.00013595367,0.00015881445,0.00010134022],"domain_scores_gemma":[0.9931177,0.0048138015,0.00034253421,0.00053865486,0.00086713367,0.00032023908],"candidate_categories":["insufficient_payload"],"consensus_categories":[],"category_scores_codex":[0.0009059747,0.0012845583,0.0017321339,0.001947048,0.0011702692,0.0017010488,0.0020946118,0.001274693,0.8873271],"category_scores_gemma":[0.007578467,0.00086604286,0.0012672818,0.0027963347,0.0003750857,0.0017154205,0.0011037093,0.0013507812,0.2557295],"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":[0.00042428993,0.00009627763,0.0018842815,0.0020653647,0.000055471068,0.00014596044,0.0000861556,0.00044980677,0.0012261744,0.00087209634,0.9840847,0.008609384],"study_design_scores_gemma":[0.004625953,0.00038774888,0.041760806,0.0023754232,0.00027208633,0.0012337121,0.00047636768,0.003009687,0.0072992234,0.016135164,0.92213583,0.00028799198],"about_ca_topic_score_codex":0.0069574444,"about_ca_topic_score_gemma":0.011450258,"teacher_disagreement_score":0.8873271,"about_ca_system_score_codex":0.0010730957,"about_ca_system_score_gemma":0.0013447183,"threshold_uncertainty_score":0.16071415},"labels":[],"label_agreement":null},{"id":"W6981561337","doi":"","title":"Equipment of the Canadian Infantrymen, 1939â1982: A Material/Historical Assessment","year":2012,"lang":"en","type":"article","venue":"Scholars Commons (Wilfrid Laurier University)","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":0,"is_retracted":false,"has_abstract":true,"route_ca_aff":false,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":true,"ca_institutions":"","funders":"","keywords":"Nucleofection; TSG101; Gestational period; Hyporeflexia; Diafiltration; Pretext; Demotion; Fusible alloy","score_opus":0.01137819886418987,"score_gpt":0.21724751768928485,"score_spread":0.205869318825095,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W6981561337","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.6804753,0.020291377,0.00060307776,0.007483286,0.00016293826,0.00009879624,0.0036036547,0.000052887106,0.2872287],"genre_scores_gemma":[0.9338492,0.017453542,0.0005574454,0.00032399135,0.000045522193,0.000030162193,0.00091295317,0.000035729314,0.04679148],"study_design_codex":"qualitative","study_design_gemma":"not_applicable","domain_scores_codex":[0.9987668,0.00005859408,0.000022156395,0.000095999436,0.0005771166,0.00047946008],"domain_scores_gemma":[0.998811,0.00013406172,0.00013555458,0.000032467735,0.00062203716,0.00026498895],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00079792284,0.00047867533,0.00022779316,0.008484043,0.01659464,0.0048277806,0.0017181572,0.0008116776,0.01281293],"category_scores_gemma":[0.0018782038,0.0005773924,0.00019265137,0.013204108,0.007356258,0.0013975485,0.0021440214,0.0012620697,0.0007418423],"study_design_candidate":"not_applicable","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":[0.00024125692,0.00009081765,0.1056379,0.0008657607,0.000037203303,0.0051068463,0.41191113,0.00064167654,0.001831864,0.11416731,0.03991492,0.3195534],"study_design_scores_gemma":[0.0000043774094,0.000047714704,0.2885476,0.0004395731,0.00001878071,0.0006800885,0.12827362,0.0001078557,0.0008302219,0.0010200735,0.5799705,0.000059703652],"about_ca_topic_score_codex":0.98834807,"about_ca_topic_score_gemma":0.9963121,"teacher_disagreement_score":0.110885166,"about_ca_system_score_codex":0.110885166,"about_ca_system_score_gemma":0.050501924,"threshold_uncertainty_score":0.80453193},"labels":[],"label_agreement":null},{"id":"W6986523904","doi":"","title":"Preferential maternal LOH in the IGF2R gene in breast cancer","year":2004,"lang":"en","type":"dissertation","venue":"eScholarship@McGill (McGill)","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":0,"is_retracted":false,"has_abstract":true,"route_ca_aff":false,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":true,"ca_institutions":"","funders":"","keywords":"Loss of heterozygosity; Gene silencing; Tumor suppressor gene; Allele; Breast cancer; Suppressor; Genomic imprinting; Gene; Oncogene","score_opus":0.010007778219956463,"score_gpt":0.24256093424842365,"score_spread":0.23255315602846718,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W6986523904","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.95944893,0.003036054,0.0038783227,0.0015577103,0.00023408054,0.000031517357,0.0011095151,0.00030449225,0.030399349],"genre_scores_gemma":[0.98353493,0.00096849195,0.0013691377,0.00021348314,0.000036879916,0.000015069564,0.0003269011,0.000041725227,0.01349315],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99989235,0.000015918722,0.000008727284,0.000024539004,0.000030767478,0.000027679338],"domain_scores_gemma":[0.99977,0.0000883267,0.000043915574,0.000017989412,0.000030155428,0.000049660317],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00021216192,0.00008863615,0.00013396589,0.0006580759,0.00025171085,0.0003101004,0.00016264814,0.00028444797,0.016950632],"category_scores_gemma":[0.00058771943,0.00013061763,0.00008794167,0.00024365692,0.00019047831,0.000109123735,0.00021671013,0.00023285394,0.0016361666],"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":[0.0013684139,0.00013280963,0.24651243,0.00020030506,0.00007047535,0.026785728,0.00024990708,0.0002752585,0.6007142,0.0028858664,0.00961077,0.11119386],"study_design_scores_gemma":[0.00009273685,0.0004639716,0.8149413,0.00008633777,0.000092086804,0.07725278,0.0004480732,0.00069599296,0.067563124,0.00090042077,0.037435506,0.000027706754],"about_ca_topic_score_codex":0.0025188352,"about_ca_topic_score_gemma":0.003965917,"teacher_disagreement_score":0.016950632,"about_ca_system_score_codex":0.00022951524,"about_ca_system_score_gemma":0.00022909897,"threshold_uncertainty_score":0.056705534},"labels":[],"label_agreement":null},{"id":"W6990818766","doi":"","title":"Epigenetic rRgulation in the Placenta and its Role in Fetal Growth","year":2011,"lang":"en","type":"dissertation","venue":"Library and Archives Canada (Government of Canada)","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":0,"is_retracted":false,"has_abstract":true,"route_ca_aff":false,"route_ca_fund":false,"route_ca_venue":true,"route_about_ca":false,"ca_institutions":"","funders":"","keywords":"Epigenetics; Fetus; Gene expression; DNA methylation; Gene","score_opus":0.0029103864237724516,"score_gpt":0.14994564764007634,"score_spread":0.1470352612163039,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W6990818766","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.97000295,0.020929614,0.005327153,0.00032428908,0.000023588831,0.000028144499,0.0003816336,0.000058463764,0.0029241154],"genre_scores_gemma":[0.9902762,0.0060793515,0.002009929,0.00006062229,0.000023163964,0.000021891121,0.00021068324,0.000008003282,0.0013101548],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99989104,0.000024123996,0.0000051970237,0.000035636844,0.000026157246,0.000017812212],"domain_scores_gemma":[0.9998802,0.000028346796,0.000048697228,0.000011730269,0.000015922917,0.000015007936],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00020589882,0.00016037477,0.00018112532,0.00057710137,0.00015617954,0.00039619353,0.00021752763,0.00022977755,0.0007296229],"category_scores_gemma":[0.00036604077,0.00013101667,0.00014049673,0.00034533665,0.00036898465,0.00015096016,0.00026511098,0.00019318481,0.00008923447],"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":[0.00091679883,0.000058644266,0.075480714,0.00040193397,0.000091365444,0.001103219,0.000462978,0.0007207303,0.8586241,0.002591737,0.00035893833,0.05918888],"study_design_scores_gemma":[0.000024390185,0.0005868054,0.83443445,0.000086672735,0.00012832912,0.003645217,0.00044526064,0.0018466791,0.14809597,0.0017465025,0.008929314,0.000030379504],"about_ca_topic_score_codex":0.0017795347,"about_ca_topic_score_gemma":0.0014589569,"teacher_disagreement_score":0.0017795347,"about_ca_system_score_codex":0.00026914536,"about_ca_system_score_gemma":0.00026712246,"threshold_uncertainty_score":0.0035383701},"labels":[],"label_agreement":null},{"id":"W6996532089","doi":"","title":"Spontaneous errors of imprinting in mouse embryos","year":2003,"lang":"en","type":"dissertation","venue":"eScholarship@McGill (McGill)","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":0,"is_retracted":false,"has_abstract":true,"route_ca_aff":false,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":true,"ca_institutions":"","funders":"","keywords":"Imprinting (psychology); Genomic imprinting; Embryonic stem cell; Allele; Gene; Embryo","score_opus":0.009657258820101017,"score_gpt":0.2337788373484205,"score_spread":0.2241215785283195,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W6996532089","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9771388,0.004893518,0.008756121,0.00020276444,0.000068012014,0.000049008057,0.0009049659,0.00037008096,0.0076166615],"genre_scores_gemma":[0.97177255,0.0027931263,0.0031313498,0.00006405137,0.000018087569,0.00008206339,0.00092391204,0.0001354197,0.021079477],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9994617,0.00013074068,0.00007574191,0.000101974096,0.00015473113,0.00007501572],"domain_scores_gemma":[0.99920636,0.0002009153,0.00023231686,0.00023016275,0.0000664558,0.000063859],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00065719004,0.00035209188,0.00015242698,0.0009155318,0.00027533976,0.00048654355,0.00045316303,0.0004871566,0.0019093435],"category_scores_gemma":[0.0006870028,0.00037591186,0.0003118939,0.00033004634,0.0004094693,0.00026403085,0.0003936345,0.00046973527,0.000749314],"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":[0.0002766472,0.000057160843,0.0049020327,0.00007432966,0.00004485434,0.00063140545,0.00013088589,0.0003998241,0.9729994,0.0032554318,0.00034494433,0.01688305],"study_design_scores_gemma":[0.000034621364,0.00028628623,0.018137118,0.000039613344,0.00004195779,0.0015277433,0.000048996437,0.00069100247,0.96983653,0.0006900499,0.0086512985,0.000014816451],"about_ca_topic_score_codex":0.001438049,"about_ca_topic_score_gemma":0.0022672736,"teacher_disagreement_score":0.0019093435,"about_ca_system_score_codex":0.00054097624,"about_ca_system_score_gemma":0.00030436306,"threshold_uncertainty_score":0.0063874125},"labels":[],"label_agreement":null},{"id":"W7002531279","doi":"","title":"\\n Gene Boy Came Home\\n . \\n Gene Boy revient chez lui Canada [Québec] 2007, 25 minutes","year":2008,"lang":"fr","type":"article","venue":"Érudit (Université de Montréal)","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":0,"is_retracted":false,"has_abstract":false,"route_ca_aff":false,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":true,"ca_institutions":"","funders":"","keywords":"Gene; Sequence (biology); Mutation; Period (music)","score_opus":0.00490611341446776,"score_gpt":0.14933979929379043,"score_spread":0.14443368587932268,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W7002531279","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":[0.01405484,0.027322674,0.0014028841,0.21390302,0.11474141,0.0005502215,0.009843844,0.0019472669,0.6162339],"genre_scores_gemma":[0.010228552,0.0017388727,0.00032576514,0.0056251804,0.0013968153,0.000036516252,0.0006129498,0.00019477423,0.9798406],"study_design_codex":"not_applicable","study_design_gemma":"not_applicable","domain_scores_codex":[0.99949694,0.000045360295,0.000013672234,0.00006995488,0.00017387468,0.00020015257],"domain_scores_gemma":[0.99917775,0.00004372587,0.000020090061,0.000018003582,0.00033914496,0.0004012705],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0005973234,0.0010097639,0.0006116366,0.00062052486,0.008966448,0.0018996367,0.00073151663,0.0026747978,0.17334452],"category_scores_gemma":[0.00152217,0.00047856176,0.0006302996,0.00043006628,0.0010384385,0.00070539885,0.0013685002,0.0033554446,0.052946057],"study_design_candidate":"not_applicable","study_design_consensus":"not_applicable","about_ca_topic_candidate":true,"about_ca_topic_consensus":true,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.000049807695,0.000012486409,0.0008049686,0.000020218407,0.0000042999263,0.000371262,0.0002931185,0.000025289573,0.00022113975,0.0004720339,0.9915038,0.0062216236],"study_design_scores_gemma":[0.000009315505,0.000018667957,0.0048275487,0.000070838716,0.000003888108,0.00012713026,0.00094309775,0.000023484998,0.000115451665,0.00013044129,0.99371654,0.0000136967965],"about_ca_topic_score_codex":0.7083628,"about_ca_topic_score_gemma":0.9446268,"teacher_disagreement_score":0.29163718,"about_ca_system_score_codex":0.011378405,"about_ca_system_score_gemma":0.006478514,"threshold_uncertainty_score":0.5867094},"labels":[],"label_agreement":null},{"id":"W7009757408","doi":"","title":"Étiologie du biais de l'inactivation du chromosome X (ICX) dans les cellules sanguines des femmes vieillissantes : sélection hémizygote et acquisition de mutations somatiques","year":2022,"lang":"fr","type":"dissertation","venue":"Papyrus : Institutional Repository (Université de Montréal)","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":0,"is_retracted":false,"has_abstract":true,"route_ca_aff":false,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":true,"ca_institutions":"","funders":"","keywords":"Y chromosome; Mutation; Genetic inheritance","score_opus":0.010375550707803358,"score_gpt":0.21131897041939962,"score_spread":0.20094341971159627,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W7009757408","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9962184,0.0018290513,0.0005510656,0.00007430029,0.000009766845,0.000009066254,0.000099161436,0.000014286921,0.0011950042],"genre_scores_gemma":[0.99742585,0.0007321158,0.00040190044,0.000026414082,0.000008881814,0.000009234383,0.00008813759,0.0000038303297,0.0013035907],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.99986076,0.000033006007,0.000007670332,0.000038572,0.00002586795,0.000034100594],"domain_scores_gemma":[0.9996599,0.00013389293,0.00008289787,0.000019287649,0.00006235346,0.00004167575],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00040556004,0.00015530502,0.00013498608,0.00078009866,0.00024131929,0.00048200358,0.00015396676,0.00040565903,0.0020517234],"category_scores_gemma":[0.00042615223,0.00022793679,0.00014541,0.00037106746,0.00038203108,0.00025265192,0.00020332477,0.00032921546,0.00027068658],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0011138844,0.000051162846,0.40776905,0.000165062,0.000051588468,0.00160673,0.0014883849,0.00015253994,0.5641779,0.001024583,0.00031763932,0.022081539],"study_design_scores_gemma":[0.000011308056,0.00036218355,0.94595385,0.000019061874,0.00004835132,0.0029584304,0.0009422599,0.00047779788,0.046167042,0.00023367275,0.0028128324,0.000013185139],"about_ca_topic_score_codex":0.0035811514,"about_ca_topic_score_gemma":0.0028640714,"teacher_disagreement_score":0.0035811514,"about_ca_system_score_codex":0.00028363583,"about_ca_system_score_gemma":0.00019006306,"threshold_uncertainty_score":0.007120669},"labels":[],"label_agreement":null},{"id":"W7014341601","doi":"","title":"Placental phenotypes associated with abnormal genomic imprinting on distal mouse chromosome 7","year":2011,"lang":"en","type":"other","venue":"cIRcle (University of British Columbia)","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":0,"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 Cancer Institute; Canadian Institutes of Health Research; National Institutes of Health","keywords":"Genomic imprinting; Imprinting (psychology); Phenotype; Gene; Gene silencing; Allele; X-inactivation; Chromosome; Chromosome 15","score_opus":0.005143948671483187,"score_gpt":0.1556041518590389,"score_spread":0.1504602031875557,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W7014341601","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9927695,0.0013204936,0.0023370676,0.00011920936,0.000023338021,0.000023304861,0.00068546436,0.00037424226,0.0023474935],"genre_scores_gemma":[0.99045956,0.0011628796,0.0018900391,0.00007418863,0.000017832373,0.000036540452,0.0011940734,0.00009967588,0.0050651436],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.99970573,0.000035866702,0.000031323434,0.000069398964,0.00010683287,0.00005088195],"domain_scores_gemma":[0.9995951,0.000057094527,0.00017776848,0.000043933902,0.00001467281,0.000111425055],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0001673161,0.0006214977,0.0002663666,0.0013144616,0.00015035736,0.00033990186,0.00042648177,0.00042906753,0.0026400152],"category_scores_gemma":[0.00017824225,0.0003965767,0.0003361928,0.00028639965,0.00050939264,0.000154707,0.00046195847,0.0006323062,0.00063844136],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.000113994254,0.0000112385715,0.00045706372,0.000018642035,0.000008435519,0.00047061173,0.0000147807295,0.00004591023,0.99810445,0.0001241816,0.000037795173,0.0005928999],"study_design_scores_gemma":[0.000097389486,0.0005135906,0.035863888,0.000024493369,0.00008262075,0.008983121,0.000067280336,0.0008748802,0.9492123,0.00028701883,0.0039779777,0.000015357422],"about_ca_topic_score_codex":0.00051405106,"about_ca_topic_score_gemma":0.000698251,"teacher_disagreement_score":0.0026400152,"about_ca_system_score_codex":0.00034587883,"about_ca_system_score_gemma":0.0001862334,"threshold_uncertainty_score":0.008831739},"labels":[],"label_agreement":null},{"id":"W7025249809","doi":"","title":"Visitor Statistics (Second Quarter 2017)","year":2017,"lang":"en","type":"article","venue":"eVols (University of Hawaii)","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":0,"is_retracted":false,"has_abstract":true,"route_ca_aff":false,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":true,"ca_institutions":"","funders":"","keywords":"Quarter (Canadian coin); Visitor pattern; Statistical analysis; Descriptive statistics; Official statistics","score_opus":0.0093110109981566,"score_gpt":0.22116217715698588,"score_spread":0.2118511661588293,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W7025249809","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":[0.0018441657,0.0011789543,0.00048487863,0.0030571786,0.0023284254,0.00015971936,0.8949139,0.002614451,0.09341838],"genre_scores_gemma":[0.008068043,0.0025470173,0.0006592887,0.0011674959,0.000917374,0.00048826812,0.52602726,0.0016052893,0.4585199],"study_design_codex":"not_applicable","study_design_gemma":"observational","domain_scores_codex":[0.99902916,0.00010060083,0.00013039514,0.00012594475,0.0004450606,0.00016885139],"domain_scores_gemma":[0.9936494,0.0006798155,0.00054966053,0.00045408073,0.0040752534,0.00059180555],"candidate_categories":["insufficient_payload"],"consensus_categories":[],"category_scores_codex":[0.0008228877,0.0006800979,0.00068246253,0.0043985276,0.00056404964,0.0021090785,0.0009843619,0.0006985309,0.32389852],"category_scores_gemma":[0.010031866,0.00041488447,0.00041062673,0.010215262,0.00020070578,0.0012477861,0.0013200112,0.0014308194,0.3149151],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.000015503396,0.000004570827,0.0003889155,0.000048432714,0.000001962698,0.000004499431,0.000009003433,0.000026254851,0.000009392692,0.00018377455,0.9930379,0.0062698293],"study_design_scores_gemma":[0.000031554184,0.00001600875,0.011674175,0.00022028801,0.0000056569593,0.000021737334,0.00013233053,0.00028775862,0.00008215132,0.00034959006,0.98716134,0.000017279832],"about_ca_topic_score_codex":0.12481208,"about_ca_topic_score_gemma":0.105584264,"teacher_disagreement_score":0.32389852,"about_ca_system_score_codex":0.0020203672,"about_ca_system_score_gemma":0.004096702,"threshold_uncertainty_score":0.9643767},"labels":[],"label_agreement":null},{"id":"W7027120210","doi":"","title":"Characterization of molecular mechanisms underlying the neurogenic effect of the bHLH protein Hes6","year":2004,"lang":"en","type":"dissertation","venue":"eScholarship@McGill (McGill)","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":0,"is_retracted":false,"has_abstract":true,"route_ca_aff":false,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":true,"ca_institutions":"","funders":"","keywords":"HEK 293 cells; Central nervous system; Context (archaeology); Signal transduction; Component (thermodynamics)","score_opus":0.008477156222236971,"score_gpt":0.2248475464572891,"score_spread":0.21637039023505214,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W7027120210","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.979506,0.00454787,0.005430708,0.00034888505,0.00004662097,0.000031649408,0.0005960861,0.00005778362,0.009434533],"genre_scores_gemma":[0.9717065,0.003670458,0.003511968,0.000111756024,0.0000226361,0.000025741516,0.0019145497,0.00004674176,0.01898975],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99993944,0.000007005433,0.0000051238626,0.0000131905845,0.000022021626,0.000013236264],"domain_scores_gemma":[0.99987996,0.00003529538,0.000021685726,0.000018003304,0.000016615531,0.000028432993],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00014151062,0.0001460648,0.0001292466,0.00022563267,0.0001887402,0.0003955128,0.00027861766,0.00023212885,0.002650051],"category_scores_gemma":[0.0001343913,0.00014617403,0.0002212672,0.000119662,0.00022787681,0.00031128316,0.00026649414,0.00054680475,0.0011041794],"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":[0.000070205635,0.000009735126,0.00026341312,0.000024829944,0.0000028442364,0.000059926027,0.000019118395,0.00005233285,0.9971499,0.00048458172,0.00003700967,0.001826064],"study_design_scores_gemma":[0.000013178337,0.00008632355,0.019190738,0.000012743036,0.0000141180135,0.00039836502,0.000098784105,0.0009376228,0.9733594,0.00037313843,0.0055102683,0.000005169262],"about_ca_topic_score_codex":0.000656994,"about_ca_topic_score_gemma":0.0009297787,"teacher_disagreement_score":0.002650051,"about_ca_system_score_codex":0.00030414204,"about_ca_system_score_gemma":0.0001723098,"threshold_uncertainty_score":0.008865297},"labels":[],"label_agreement":null},{"id":"W7027226843","doi":"","title":"Conflict And Solidarity Between Anti-Colonial Environmentalism, Indigenous Anti-Pipeline Resistance, And The Labour","year":2025,"lang":"en","type":"other","venue":"York University Digital Library (York University)","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":0,"is_retracted":false,"has_abstract":true,"route_ca_aff":false,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":true,"ca_institutions":"","funders":"","keywords":"Solidarity; Indigenous; Resistance (ecology); Colonialism; Dilemma; Witness; Investment (military); Government (linguistics)","score_opus":0.005045456279234641,"score_gpt":0.16410674898363098,"score_spread":0.15906129270439634,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W7027226843","genre_codex":"other","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":[0.43804106,0.0038256506,0.0024292304,0.05819303,0.00015017546,0.000048528924,0.000060055372,0.000029405604,0.49722278],"genre_scores_gemma":[0.98200077,0.0011872053,0.00036522094,0.001450678,0.000020103134,0.000011529548,0.000012026428,0.000009975138,0.014942431],"study_design_codex":"theoretical_or_conceptual","study_design_gemma":"qualitative","domain_scores_codex":[0.99650264,0.0008376564,0.000035578043,0.00022116955,0.0006576797,0.0017453746],"domain_scores_gemma":[0.9984415,0.00062384317,0.0002173436,0.00007646902,0.00024276556,0.00039802707],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.002270084,0.00025523288,0.0002406548,0.0010339337,0.024620207,0.012506024,0.0010911282,0.0018374458,0.003213112],"category_scores_gemma":[0.0027624392,0.0001804704,0.0001998497,0.0017780776,0.036777023,0.0033015185,0.0052868,0.0035103522,0.00017083075],"study_design_candidate":"qualitative","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":[0.000027046677,0.000028199078,0.0056977645,0.000076029544,0.000015388056,0.0005629101,0.29961467,0.0003720364,0.0005037595,0.664504,0.007213215,0.021385036],"study_design_scores_gemma":[0.0000074084014,0.000023816176,0.019336877,0.00039168826,0.000026050951,0.00020421193,0.62693566,0.0004129008,0.0005619541,0.060187165,0.29187268,0.000039561717],"about_ca_topic_score_codex":0.8422574,"about_ca_topic_score_gemma":0.9322966,"teacher_disagreement_score":0.15774262,"about_ca_system_score_codex":0.063935876,"about_ca_system_score_gemma":0.06269799,"threshold_uncertainty_score":0.46388942},"labels":[],"label_agreement":null},{"id":"W7035931548","doi":"","title":"Alberta's Response to the Criticism of the Oil Sands","year":2011,"lang":"en","type":"other","venue":"","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":0,"is_retracted":false,"has_abstract":false,"route_ca_aff":false,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":true,"ca_institutions":"","funders":"","keywords":"Criticism; Oil sands; Petroleum; Oil exploration","score_opus":0.008224423501912994,"score_gpt":0.2288817281846325,"score_spread":0.22065730468271952,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W7035931548","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":[0.00017150903,0.0058872076,0.00019820365,0.92315614,0.048695818,0.000007558563,0.000071370116,0.0001058242,0.021706374],"genre_scores_gemma":[0.0044659125,0.0046157814,0.00047135795,0.77853674,0.033184696,0.000027756241,0.00006419611,0.00023614819,0.17839746],"study_design_codex":"not_applicable","study_design_gemma":"not_applicable","domain_scores_codex":[0.99780196,0.00033705693,0.00009421894,0.00026938002,0.0011557864,0.00034154786],"domain_scores_gemma":[0.9902952,0.0036496972,0.00023568374,0.00042094983,0.0029447281,0.0024538725],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0036802376,0.0007812134,0.0009205267,0.0017310567,0.0045224964,0.0047921827,0.0030542808,0.023924714,0.03308549],"category_scores_gemma":[0.016049052,0.00065738667,0.0006226989,0.0013241223,0.0044582924,0.0023544468,0.0025841948,0.024850283,0.009600779],"study_design_candidate":"not_applicable","study_design_consensus":"not_applicable","about_ca_topic_candidate":true,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0000048573315,0.0000023007337,0.00003150757,0.000009148969,0.0000011397487,0.000051544364,0.000017986318,0.000014174553,0.000013513449,0.0012633274,0.9961511,0.0024396018],"study_design_scores_gemma":[0.000008468522,0.0000030647122,0.00025200192,0.00007500409,0.000003030672,0.00013366807,0.00007456441,0.00003813636,0.000037668487,0.0009034197,0.9984609,0.000010169129],"about_ca_topic_score_codex":0.10506561,"about_ca_topic_score_gemma":0.2888323,"teacher_disagreement_score":0.8949344,"about_ca_system_score_codex":0.0057609947,"about_ca_system_score_gemma":0.008389124,"threshold_uncertainty_score":0.20890814},"labels":[],"label_agreement":null},{"id":"W7038500911","doi":"","title":"JFE Shoji Power Canada 5-part series: Part 1","year":2022,"lang":"en","type":"other","venue":"Bulletin of Miscellaneous Information (Royal Gardens Kew)","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":0,"is_retracted":false,"has_abstract":true,"route_ca_aff":false,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":true,"ca_institutions":"","funders":"","keywords":"Power (physics); Market power; Hydro power; Competition (biology)","score_opus":0.003719003126380845,"score_gpt":0.16499147767262493,"score_spread":0.16127247454624408,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W7038500911","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":[0.0006002744,0.0028768526,0.0008095614,0.0069944365,0.0074510477,0.0002242899,0.0045661572,0.0015450543,0.97493243],"genre_scores_gemma":[0.0005880444,0.0006576123,0.00014770271,0.0003384525,0.00026397812,0.000017834103,0.00057308865,0.00024649294,0.9971667],"study_design_codex":"not_applicable","study_design_gemma":"not_applicable","domain_scores_codex":[0.9991035,0.00003666348,0.000020385038,0.00008647871,0.0005960988,0.00015685188],"domain_scores_gemma":[0.9951906,0.00022316765,0.00010032235,0.00021986726,0.0027761841,0.0014898154],"candidate_categories":["insufficient_payload"],"consensus_categories":["insufficient_payload"],"category_scores_codex":[0.0009859158,0.001132296,0.00063832273,0.0019783482,0.0029492343,0.0044572153,0.0011780912,0.0019126476,0.681997],"category_scores_gemma":[0.0027610208,0.00064081117,0.00039416153,0.002490349,0.0010598338,0.0016175321,0.0014091495,0.0017592291,0.5091333],"study_design_candidate":"not_applicable","study_design_consensus":"not_applicable","about_ca_topic_candidate":true,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0000075994335,0.000008692767,0.00006384982,0.000023454697,3.9503118e-7,0.0000139494,0.0000087504495,0.000020138254,0.00010995151,0.00031106477,0.981458,0.017974075],"study_design_scores_gemma":[0.0000027079213,0.000004251302,0.00044290716,0.000024206898,5.8945545e-7,0.000020345642,0.000022430142,0.000026442201,0.00007104124,0.00009699941,0.9992841,0.000004055027],"about_ca_topic_score_codex":0.24778202,"about_ca_topic_score_gemma":0.49226066,"teacher_disagreement_score":0.752218,"about_ca_system_score_codex":0.0052953837,"about_ca_system_score_gemma":0.016469643,"threshold_uncertainty_score":0.49267954},"labels":[],"label_agreement":null},{"id":"W7084600370","doi":"10.1007/978-3-031-95288-3_32","title":"Predicting the Thermal Performance of Concrete Floor Slabs Connected to Balconies Through Thermal Breaks","year":2025,"lang":"en","type":"book-chapter","venue":"Lecture notes in civil engineering","topic":"Genetic Syndromes and Imprinting","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":"Inro Consultants (Canada); Western University","funders":"","keywords":"Thermal transmittance; Thermal; Slab; Envelope (radar); Classification of discontinuities; Energy consumption; Building envelope; Heat flow","score_opus":0.005516717204196268,"score_gpt":0.19740018646219423,"score_spread":0.19188346925799796,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W7084600370","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9967476,0.000029697772,0.0014730135,0.000013935748,0.0000055655582,0.000007930361,0.0005664161,0.00008430799,0.0010715084],"genre_scores_gemma":[0.9972517,0.000024844108,0.0010828506,0.0000032592918,0.000002515182,0.000007728842,0.0009051599,0.000019958465,0.0007019606],"study_design_codex":"simulation_or_modeling","study_design_gemma":"simulation_or_modeling","domain_scores_codex":[0.99986756,0.000013084821,0.0000055300734,0.00004441804,0.000025995883,0.000043482552],"domain_scores_gemma":[0.9998042,0.00008410992,0.000022241069,0.000012677015,0.00004507961,0.000031745487],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00017826246,0.00079164805,0.0004766442,0.0007033683,0.00053929427,0.0007582786,0.0006490045,0.00080122345,0.0021012712],"category_scores_gemma":[0.0004460451,0.00054707186,0.0006406518,0.00088138774,0.00034594774,0.00044112295,0.00034391668,0.0005387982,0.0007136444],"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":[0.0006625995,0.00022807899,0.20794788,0.000075794196,0.0001500173,0.00023109278,0.00021183466,0.7422034,0.023924742,0.00023632564,0.0009647452,0.023163466],"study_design_scores_gemma":[0.000015211138,0.00010717575,0.26893845,0.000012574592,0.000039822273,0.000026479405,0.00043339937,0.7259806,0.003898733,0.00022262742,0.00029883487,0.000026188114],"about_ca_topic_score_codex":0.07259733,"about_ca_topic_score_gemma":0.1186822,"teacher_disagreement_score":0.07259733,"about_ca_system_score_codex":0.0009317615,"about_ca_system_score_gemma":0.00054935325,"threshold_uncertainty_score":0.14434952},"labels":[],"label_agreement":null},{"id":"W7087864474","doi":"","title":"MJM MedTalks (S02E11): Global Surgery in our “Backyard”; A Discussion with Dr. Evan Wong","year":2025,"lang":"en","type":"article","venue":"DOAJ (DOAJ: Directory of Open Access Journals)","topic":"Genetic Syndromes and Imprinting","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":true,"ca_institutions":"Montreal General Hospital; McGill University Health Centre","funders":"","keywords":"Conversation; Glossary; Medical journal; Alternative medicine; Medical advice; Space (punctuation); Health care","score_opus":0.10068166216111152,"score_gpt":0.5066879391136836,"score_spread":0.4060062769525721,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W7087864474","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":[0.0032809854,0.00338176,0.00031307858,0.83336854,0.113447815,0.000116649906,0.00031400257,0.00018757692,0.045589577],"genre_scores_gemma":[0.037609402,0.0030759452,0.0010251258,0.6242048,0.04535247,0.00028881175,0.00027712338,0.00047623637,0.28769004],"study_design_codex":"not_applicable","study_design_gemma":"not_applicable","domain_scores_codex":[0.9973009,0.00091628503,0.00009192841,0.00018758402,0.00059397786,0.00090932834],"domain_scores_gemma":[0.990986,0.001686633,0.00029876074,0.00019074319,0.0009658157,0.0058719846],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0056967004,0.00058588246,0.0005576916,0.00050431286,0.013067377,0.00647168,0.0015876392,0.010654768,0.08286541],"category_scores_gemma":[0.012132878,0.00054858613,0.0008042488,0.0004998125,0.0033312803,0.0042827916,0.0069775563,0.016963556,0.0131773865],"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":[0.000012452378,0.000014587266,0.00009073742,0.000025718176,9.4050756e-7,0.00028288178,0.0010911812,0.000005976431,0.000067361485,0.0007861755,0.99538654,0.0022353593],"study_design_scores_gemma":[0.000009972535,0.00001895827,0.0008002831,0.000121948615,0.0000016173217,0.00026637982,0.0056488747,0.000019707879,0.000057879395,0.00029731472,0.99274397,0.000013124911],"about_ca_topic_score_codex":0.022651,"about_ca_topic_score_gemma":0.076988734,"teacher_disagreement_score":0.08286541,"about_ca_system_score_codex":0.006475808,"about_ca_system_score_gemma":0.005669849,"threshold_uncertainty_score":0.27721244},"labels":[],"label_agreement":null},{"id":"W7093955905","doi":"","title":"Marley's Journey","year":2018,"lang":"","type":"article","venue":"Scholarship at UWindsor (University of Windsor)","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":0,"is_retracted":false,"has_abstract":true,"route_ca_aff":false,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":true,"ca_institutions":"","funders":"","keywords":"Angelman syndrome; Girl; Storytelling; Schedule; Documentary film; Character (mathematics)","score_opus":0.018462896464875325,"score_gpt":0.2310371623334759,"score_spread":0.21257426586860056,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W7093955905","genre_codex":"other","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":[0.069151714,0.023774842,0.002898063,0.3433319,0.028684102,0.0003583346,0.000923185,0.0005258971,0.53035206],"genre_scores_gemma":[0.22922471,0.018604787,0.005652824,0.054107945,0.0021772773,0.00024285541,0.0004871324,0.00047894072,0.68902355],"study_design_codex":"not_applicable","study_design_gemma":"case_report","domain_scores_codex":[0.9977071,0.0008105643,0.00007112585,0.00027810587,0.00058352586,0.0005494953],"domain_scores_gemma":[0.99561584,0.00033145057,0.00020694504,0.000110155845,0.0007803476,0.0029552546],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0015024365,0.0008119328,0.00045182978,0.00069268426,0.018421343,0.0072421106,0.0015339793,0.0032082286,0.055150703],"category_scores_gemma":[0.006904286,0.00043023442,0.00052701856,0.0007075375,0.0031861889,0.0054542203,0.0072125946,0.009103334,0.012828748],"study_design_candidate":"case_report","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.000045808527,0.00006911072,0.0011427182,0.00019695213,0.000009971376,0.0070490045,0.11667163,0.00008936575,0.00079298206,0.038449593,0.77885205,0.056630787],"study_design_scores_gemma":[0.0000014813235,0.000021631764,0.00027156554,0.0001482819,0.000001688137,0.0014665329,0.028561108,0.000016454567,0.000051469127,0.001227722,0.96821934,0.00001274542],"about_ca_topic_score_codex":0.04417086,"about_ca_topic_score_gemma":0.12295477,"teacher_disagreement_score":0.055150703,"about_ca_system_score_codex":0.006906588,"about_ca_system_score_gemma":0.011726543,"threshold_uncertainty_score":0.18449748},"labels":[],"label_agreement":null},{"id":"W7095003899","doi":"10.5281/zenodo.17442667","title":"Cheilosia (Cheilosia) pseudogrossa Stackelberg 1968","year":2025,"lang":"","type":"article","venue":"Zenodo (CERN European Organization for Nuclear Research)","topic":"Genetic Syndromes and Imprinting","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":"University of Ottawa","funders":"","keywords":"Apex (geometry); Stackelberg competition; Cluster (spacecraft); Face (sociological concept); Differential (mechanical device)","score_opus":0.019091397514554513,"score_gpt":0.2523788569098605,"score_spread":0.23328745939530598,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W7095003899","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":[0.5230887,0.01629237,0.0063228146,0.0007332883,0.00052748993,0.0007611856,0.0039147777,0.0009494172,0.44741002],"genre_scores_gemma":[0.97628945,0.0020523472,0.0039470657,0.000428925,0.000114617986,0.00008749631,0.0012170383,0.00004902073,0.01581392],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.99982846,0.00001828451,0.00001697611,0.000053050568,0.000050323837,0.000032968223],"domain_scores_gemma":[0.9997912,0.000038520244,0.00008498576,0.000027920807,0.000040583793,0.000016752414],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00009798787,0.000906061,0.000259642,0.0021640798,0.0017281857,0.00053678907,0.00048958824,0.0008800685,0.012684467],"category_scores_gemma":[0.00047384505,0.0003071917,0.00038473596,0.00095323514,0.00080491503,0.0009045459,0.0011280166,0.00063455076,0.0037313693],"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":[0.00085048587,0.00021092239,0.05071653,0.0012453498,0.00021153617,0.006835381,0.0023057556,0.0017928386,0.08724246,0.01080332,0.0292051,0.8085803],"study_design_scores_gemma":[0.00015789173,0.00041519426,0.5173757,0.0008570825,0.00022821217,0.03292918,0.0020571693,0.0011756327,0.009212358,0.004151424,0.4313323,0.000107843494],"about_ca_topic_score_codex":0.0071223355,"about_ca_topic_score_gemma":0.0131461965,"teacher_disagreement_score":0.012684467,"about_ca_system_score_codex":0.00064309756,"about_ca_system_score_gemma":0.00029709586,"threshold_uncertainty_score":0.04243374},"labels":[],"label_agreement":null},{"id":"W7097295217","doi":"","title":"MICHAELA MÜLLER CHARACTERIZATION OF A NEW LARGE FAMILY OF EXTINCT SHORT RETROPOSONS IN THE PROTOZOAN PARASITE LEISHMANIA AND THEIR ROLE IN POST-TRANSCRIPTIONAL REGULATION OF GENE EXPRESSION","year":2015,"lang":"en","type":"article","venue":"","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":0,"is_retracted":false,"has_abstract":true,"route_ca_aff":false,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":true,"ca_institutions":"","funders":"","keywords":"Retroposon; Gene; Leishmania; Protozoan parasite; Gene expression; Parasite hosting; Expression (computer science)","score_opus":0.014579935964184743,"score_gpt":0.23551275708582398,"score_spread":0.22093282112163923,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W7097295217","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9491773,0.009819459,0.018250851,0.004758192,0.0007069185,0.000098964316,0.00081725174,0.00016810637,0.016202904],"genre_scores_gemma":[0.89508504,0.011990337,0.02245363,0.0010081677,0.00032598426,0.00011284457,0.0016361792,0.00017987254,0.067208],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9998535,0.000023641756,0.00000854894,0.000048173282,0.00005082652,0.000015280651],"domain_scores_gemma":[0.9997603,0.00009072474,0.000035338304,0.000017686845,0.00003599174,0.00005988435],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00032099526,0.00016492353,0.00013113441,0.0004904332,0.00035252934,0.00056007673,0.00025651342,0.00029117538,0.003255586],"category_scores_gemma":[0.00044454564,0.00013932232,0.00018281875,0.00023869984,0.00034278442,0.00033657716,0.00041658388,0.0007938853,0.000980947],"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":[0.0005696986,0.00004835672,0.009604276,0.00019529246,0.00002251309,0.0007460415,0.0005935854,0.0005768506,0.90362084,0.008362482,0.0020421352,0.07361781],"study_design_scores_gemma":[0.000070377886,0.0010552752,0.096788935,0.00011402833,0.000059728252,0.0047825524,0.00086063205,0.0033385276,0.6601746,0.007084598,0.22557135,0.00009938976],"about_ca_topic_score_codex":0.0006214488,"about_ca_topic_score_gemma":0.00091626396,"teacher_disagreement_score":0.003255586,"about_ca_system_score_codex":0.00031683146,"about_ca_system_score_gemma":0.00034504,"threshold_uncertainty_score":0.010890961},"labels":[],"label_agreement":null},{"id":"W7099903259","doi":"","title":"DOI: 10.1007/s00268-001-0279-x WORLD Journal of SURGERY","year":2002,"lang":"en","type":"article","venue":"","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":0,"is_retracted":false,"has_abstract":true,"route_ca_aff":false,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":true,"ca_institutions":"","funders":"","keywords":"Sigmoidoscopy; Hematocrit; Aspirin; Orthostatic vital signs; Blood loss; Phlebotomy; Disease","score_opus":0.026740635851965542,"score_gpt":0.22990150805316908,"score_spread":0.20316087220120355,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W7099903259","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":[0.03751004,0.014515635,0.0021452154,0.0053094616,0.0028350472,0.00041201708,0.0031251824,0.0007814457,0.9333659],"genre_scores_gemma":[0.038969368,0.009288596,0.0045271195,0.002659413,0.0054213773,0.00027535533,0.004197212,0.00041366942,0.9342478],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.99912864,0.00017275068,0.0001235697,0.00017037551,0.0002337925,0.00017096227],"domain_scores_gemma":[0.9975987,0.0007261017,0.00025032833,0.00014278959,0.00042777375,0.0008543359],"candidate_categories":["insufficient_payload"],"consensus_categories":["insufficient_payload"],"category_scores_codex":[0.0013266286,0.0012805717,0.00071154255,0.0017240412,0.00046180285,0.000995726,0.00089138275,0.0015131882,0.7395671],"category_scores_gemma":[0.0014554302,0.00038409632,0.00063454016,0.0011024914,0.0006423738,0.0016120984,0.001160408,0.001303908,0.6847537],"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":[0.0010266792,0.00061963114,0.025012674,0.00075744645,0.000098820215,0.002495397,0.0000713976,0.00014967856,0.0036944437,0.00080877193,0.10917902,0.85608613],"study_design_scores_gemma":[0.00032803975,0.0015727622,0.094667494,0.0019511151,0.000118075724,0.024245784,0.00029143342,0.00093071576,0.0014142729,0.0008467094,0.8735695,0.000063984386],"about_ca_topic_score_codex":0.0011445306,"about_ca_topic_score_gemma":0.0015348252,"teacher_disagreement_score":0.2604329,"about_ca_system_score_codex":0.00041668376,"about_ca_system_score_gemma":0.0005932689,"threshold_uncertainty_score":0.37147588},"labels":[],"label_agreement":null},{"id":"W7100321571","doi":"","title":"Does Distance Still Matter in the Age of the Internet?","year":2011,"lang":"en","type":"article","venue":"","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":0,"is_retracted":false,"has_abstract":true,"route_ca_aff":false,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":true,"ca_institutions":"","funders":"","keywords":"Social distance; Interpersonal communication; Distance education; Interpersonal relationship; Phone; Geographical distance","score_opus":0.01056121854065204,"score_gpt":0.21263784390657206,"score_spread":0.20207662536592003,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W7100321571","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.86092955,0.031015666,0.001349052,0.048841607,0.0006261731,0.000015530764,0.00075090624,0.000021198743,0.05645043],"genre_scores_gemma":[0.9886994,0.006145006,0.00018351199,0.0011689403,0.00040224925,0.0000051185702,0.000101349586,0.000016113096,0.0032783542],"study_design_codex":"observational","study_design_gemma":"theoretical_or_conceptual","domain_scores_codex":[0.9992305,0.00022230312,0.000057289108,0.00017306283,0.00015664248,0.00016024082],"domain_scores_gemma":[0.9948762,0.0020326492,0.0011607802,0.0002661619,0.00055211067,0.0011122406],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0011644308,0.00014145073,0.000428414,0.000964872,0.0010305184,0.003248819,0.00051180157,0.0010519561,0.009205672],"category_scores_gemma":[0.011385273,0.000113420254,0.00020012067,0.0015492042,0.0018752365,0.0049021295,0.0011728823,0.0013586651,0.00095887634],"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":[0.000537645,0.00017566857,0.6299469,0.0004170993,0.00019146143,0.0010613779,0.0316778,0.00036114012,0.0015068788,0.12768248,0.0100827925,0.19635889],"study_design_scores_gemma":[0.000021299385,0.0003173643,0.81809783,0.0004921948,0.00015346135,0.0015847542,0.03650313,0.0003357221,0.00067050266,0.042799827,0.098955445,0.000068515044],"about_ca_topic_score_codex":0.007220168,"about_ca_topic_score_gemma":0.009014369,"teacher_disagreement_score":0.009205672,"about_ca_system_score_codex":0.00087955844,"about_ca_system_score_gemma":0.00058137556,"threshold_uncertainty_score":0.030796051},"labels":[],"label_agreement":null},{"id":"W7100427132","doi":"","title":"© 2003 Canadian Medical Association or its licensors","year":2003,"lang":"en","type":"article","venue":"","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":0,"is_retracted":false,"has_abstract":true,"route_ca_aff":false,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":true,"ca_institutions":"","funders":"","keywords":"Association (psychology); MEDLINE; Disease; Epidemiology","score_opus":0.008659148788515756,"score_gpt":0.23585082484500236,"score_spread":0.2271916760564866,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W7100427132","genre_codex":"review","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":[0.0016998204,0.843528,0.00046603693,0.056593947,0.010290842,0.0011565157,0.044419564,0.0001260889,0.041719265],"genre_scores_gemma":[0.023052277,0.91381323,0.0031005647,0.013049616,0.0031236047,0.0011903789,0.010234387,0.000054390868,0.03238157],"study_design_codex":"not_applicable","study_design_gemma":"not_applicable","domain_scores_codex":[0.9958584,0.0010533602,0.0008945065,0.00022071903,0.0017632878,0.00020971625],"domain_scores_gemma":[0.9615555,0.012457355,0.0054777195,0.0008572513,0.017469482,0.0021827004],"candidate_categories":["insufficient_payload"],"consensus_categories":[],"category_scores_codex":[0.007201789,0.00058273476,0.0023144863,0.0072511635,0.0008929197,0.0018081029,0.0020653415,0.001953229,0.10687782],"category_scores_gemma":[0.052447136,0.00072408124,0.0016395288,0.011403251,0.0010842372,0.00093274086,0.0008205946,0.0012103469,0.011027099],"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":[0.0006508752,0.000016314072,0.0022999973,0.08294604,0.0009619354,0.00017696714,0.00007832974,0.00007417999,0.00022612134,0.00049516757,0.68881357,0.22326052],"study_design_scores_gemma":[0.0011574733,0.00011786482,0.0357697,0.1351271,0.004226334,0.0003478694,0.00022263644,0.00010915155,0.00019387293,0.0005443413,0.82212967,0.00005408275],"about_ca_topic_score_codex":0.29194513,"about_ca_topic_score_gemma":0.5862346,"teacher_disagreement_score":0.8931222,"about_ca_system_score_codex":0.005986155,"about_ca_system_score_gemma":0.045914114,"threshold_uncertainty_score":0.58049166},"labels":[],"label_agreement":null},{"id":"W7105111214","doi":"10.71781/29692","title":"Étiologie du biais de l'inactivation du chromosome X (ICX) dans les cellules sanguines des femmes vieillissantes : sélection hémizygote et acquisition de mutations somatiques","year":2022,"lang":"fr","type":"dissertation","venue":"Papyrus : Institutional Repository (Université de Montréal)","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":0,"is_retracted":false,"has_abstract":true,"route_ca_aff":false,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":true,"ca_institutions":"","funders":"","keywords":"Mutation; Population; Y chromosome; Chromosome","score_opus":0.010375550707803358,"score_gpt":0.21131897041939962,"score_spread":0.20094341971159627,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W7105111214","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99583554,0.0022474125,0.00078384555,0.000089405825,0.0000137625475,0.000012301962,0.00007188647,0.000014169212,0.00093167496],"genre_scores_gemma":[0.9975973,0.0007847374,0.00051062164,0.000030463898,0.000012525655,0.000011096987,0.0000712245,0.0000035590658,0.0009785161],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.99981135,0.000048740287,0.000011377988,0.000050170638,0.000034590365,0.000043903572],"domain_scores_gemma":[0.9995914,0.00014715925,0.00010647789,0.000025139752,0.000077808465,0.00005195721],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0005054416,0.00020249731,0.0001672464,0.0008885218,0.00028955092,0.0005262724,0.00017728847,0.00049909885,0.0016198038],"category_scores_gemma":[0.00060353964,0.00025221246,0.0001758465,0.0003579922,0.0004328594,0.00030105864,0.00021054994,0.00037691588,0.00021890228],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0012290668,0.00006040598,0.35163733,0.0001952972,0.000058386562,0.0020639545,0.0013229745,0.00018464074,0.62257665,0.0010477384,0.00026401263,0.019359523],"study_design_scores_gemma":[0.000024437046,0.0006594166,0.8991171,0.000035604386,0.00009790604,0.0061412505,0.001136115,0.0009888508,0.087165706,0.0004247223,0.0041860444,0.000022792543],"about_ca_topic_score_codex":0.00303789,"about_ca_topic_score_gemma":0.0019987216,"teacher_disagreement_score":0.00303789,"about_ca_system_score_codex":0.00031666778,"about_ca_system_score_gemma":0.0002239205,"threshold_uncertainty_score":0.006040454},"labels":[],"label_agreement":null},{"id":"W7149233415","doi":"","title":"Abstracts from the 2008 TOS Fall Symposium","year":2009,"lang":"","type":"article","venue":"Digital Commons - University of South Florida (University of South Florida)","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":0,"is_retracted":false,"has_abstract":true,"route_ca_aff":false,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":true,"ca_institutions":"","funders":"","keywords":"National park; Biodiversity; Spring (device); Taxon; Biodiversity conservation","score_opus":0.011010728880447023,"score_gpt":0.17576765909810563,"score_spread":0.1647569302176586,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W7149233415","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":[0.0028808948,0.011440218,0.000965036,0.041529354,0.16472355,0.00032256433,0.0049450924,0.000623673,0.77256954],"genre_scores_gemma":[0.0035305733,0.0028532003,0.00023835254,0.0019886869,0.00968042,0.000073865434,0.0018107202,0.00012870657,0.97969556],"study_design_codex":"not_applicable","study_design_gemma":"not_applicable","domain_scores_codex":[0.9994222,0.00006021164,0.000029553228,0.00010141339,0.00025761317,0.00012913221],"domain_scores_gemma":[0.9986291,0.000060215465,0.00004151384,0.000056043384,0.00063671183,0.0005764914],"candidate_categories":["insufficient_payload"],"consensus_categories":[],"category_scores_codex":[0.001077403,0.0009763169,0.00069148454,0.0011278722,0.0022479724,0.0035488803,0.0009821623,0.0020297572,0.50225645],"category_scores_gemma":[0.0014949399,0.00025001267,0.0006104382,0.0007259768,0.00038636662,0.0015371339,0.0026472027,0.0021850574,0.2834726],"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":[0.000047000452,0.000042849326,0.00011684324,0.000063898915,0.0000022198658,0.000032591954,0.00004111449,0.000020799971,0.00016999115,0.000500217,0.97945327,0.019509235],"study_design_scores_gemma":[0.000007068777,0.000020179787,0.00052289676,0.00008538042,0.0000023879259,0.000016719312,0.00011686948,0.000017807768,0.000042693202,0.00022268703,0.9989422,0.000003152946],"about_ca_topic_score_codex":0.004169902,"about_ca_topic_score_gemma":0.016617667,"teacher_disagreement_score":0.50225645,"about_ca_system_score_codex":0.0016384372,"about_ca_system_score_gemma":0.0024491246,"threshold_uncertainty_score":0.7099707},"labels":[],"label_agreement":null},{"id":"W75734716","doi":"10.1023/a:1026592318341","title":"Parental Imprinting in Drosophila","year":2000,"lang":"en","type":"review","venue":"Genetica","topic":"Genetic Syndromes and Imprinting","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":"Dalhousie University","funders":"","keywords":"Imprinting (psychology); Genomic imprinting; Biology; Heterochromatin; Genetics; Epigenetics; Drosophila melanogaster; Chromatin; Gene silencing; DNA methylation; Gene; Evolutionary biology; Gene expression","score_opus":0.0219007618739802,"score_gpt":0.29581888315751415,"score_spread":0.27391812128353393,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W75734716","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":[0.0002788674,0.9962147,0.0005787112,0.0001682943,0.00046490578,0.0000052892024,0.000026417656,0.000019595085,0.0022431859],"genre_scores_gemma":[0.001886841,0.9933814,0.0006761147,0.00026812058,0.00046180328,0.000011232317,0.00007840819,0.0000034692087,0.0032327087],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.9998894,0.000013277967,0.000014337011,0.000025742096,0.000043851716,0.000013396587],"domain_scores_gemma":[0.99989176,0.000036895042,0.000019044977,0.000007711107,0.000023954042,0.000020601818],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.000414822,0.001360593,0.001487555,0.0019175357,0.0004104181,0.0011481582,0.0016475666,0.0011976759,0.0026948764],"category_scores_gemma":[0.00029699193,0.00060607947,0.00035283362,0.0023567025,0.001102041,0.0013603417,0.0006593877,0.0017577283,0.0023524167],"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":[0.00014362845,0.00007894343,0.00021841613,0.0077235964,0.000081131046,0.0004963349,0.00008461141,0.0014447456,0.010981542,0.0109204,0.043770276,0.9240564],"study_design_scores_gemma":[0.000022253595,0.000034174755,0.00068732165,0.00078303186,0.00006275702,0.0009982185,0.00003646498,0.00013648512,0.0017774884,0.0032390463,0.9922085,0.0000143517445],"about_ca_topic_score_codex":0.0017455277,"about_ca_topic_score_gemma":0.0024411203,"teacher_disagreement_score":0.0026948764,"about_ca_system_score_codex":0.001149611,"about_ca_system_score_gemma":0.00073385745,"threshold_uncertainty_score":0.009015262},"labels":[],"label_agreement":null},{"id":"W769689815","doi":"10.1096/fasebj.29.1_supplement.lb34","title":"TMED2 is Sufficient for Trophoblast Fusion","year":2015,"lang":"en","type":"article","venue":"The FASEB Journal","topic":"Genetic Syndromes and Imprinting","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":"McGill University; McGill Genome Centre","funders":"","keywords":"Syncytiotrophoblast; Cell fusion; Cell biology; Syncytium; Cytotrophoblast; Gene knockdown; Trophoblast; Chemistry; Biology; Molecular biology; Cell culture; Placenta; Fetus; Genetics","score_opus":0.023448337501254173,"score_gpt":0.2570063313903431,"score_spread":0.23355799388908896,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W769689815","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9698608,0.0035718281,0.011609151,0.0007057118,0.0003043938,0.00011328702,0.00791616,0.0005183219,0.005400327],"genre_scores_gemma":[0.9732015,0.00095593143,0.0045235497,0.00019077338,0.000022196544,0.00010473187,0.0117353555,0.00018103243,0.009085008],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9995708,0.00005955097,0.00007395324,0.0001026459,0.00012987085,0.00006308898],"domain_scores_gemma":[0.99960107,0.00010487832,0.000074003314,0.00006447829,0.000053254877,0.000102372935],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0002937008,0.0004427611,0.0003877475,0.00032894374,0.00033403776,0.00065408385,0.00030008028,0.00063326,0.00290487],"category_scores_gemma":[0.000395352,0.00031647552,0.0004548821,0.00025601132,0.00025852845,0.00028006407,0.0006127096,0.0007719804,0.0014042625],"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":[0.000070954324,0.000017144914,0.00019618451,0.000056763347,0.000008327125,0.00014043745,0.000016275213,0.000049331855,0.99860317,0.00013532361,0.00015827361,0.00054783566],"study_design_scores_gemma":[0.00003513428,0.000106530264,0.005742193,0.000018894145,0.00003197719,0.0011306972,0.000053164473,0.0019673298,0.9699795,0.000107811815,0.02081417,0.000012591352],"about_ca_topic_score_codex":0.00082375255,"about_ca_topic_score_gemma":0.0010542214,"teacher_disagreement_score":0.00290487,"about_ca_system_score_codex":0.0005834873,"about_ca_system_score_gemma":0.00036017637,"threshold_uncertainty_score":0.009717703},"labels":[],"label_agreement":null},{"id":"W85551801","doi":"10.1007/978-0-387-73693-8_24","title":"Neurodevelopmental Abnormalities in the Brainstem of Prenatal Mice Lacking the Prader-Willi Syndrome Gene Necdin","year":2007,"lang":"en","type":"article","venue":"Advances in experimental medicine and biology","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":11,"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","funders":"Alberta Heritage Foundation for Medical Research","keywords":"Brainstem; Failure to thrive; Neurodevelopmental disorder; Hypotonia; Medicine; Endocrinology; Internal medicine; Pediatrics; Autism; Psychiatry","score_opus":0.020183711785846745,"score_gpt":0.3135054386557513,"score_spread":0.29332172686990454,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W85551801","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9956226,0.00073807745,0.0017314248,0.00015801913,0.000043392025,0.000009828755,0.00051809713,0.00012440451,0.0010542386],"genre_scores_gemma":[0.99125504,0.00090447837,0.0021114366,0.000072404066,0.000011070354,0.000028229644,0.0004492086,0.000092690236,0.0050754277],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99975914,0.000025726524,0.000025159441,0.00006684296,0.000080231206,0.000042941152],"domain_scores_gemma":[0.9996153,0.00007836213,0.00013087741,0.000031902695,0.000033185108,0.000110434354],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00013221332,0.00063843373,0.0003951075,0.0009648077,0.0002374697,0.00033541728,0.00037582032,0.00056172203,0.002815578],"category_scores_gemma":[0.0002780771,0.00038581563,0.00021371651,0.00017504016,0.0006804966,0.00034545898,0.00039858202,0.001113359,0.00035375025],"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":[0.00017060067,0.000022042432,0.0003233254,0.000026707028,0.00000898581,0.0005512061,0.0000412754,0.000062950196,0.9974776,0.00022808478,0.00004216542,0.0010450104],"study_design_scores_gemma":[0.00005765171,0.0003317864,0.032243505,0.000028069719,0.00007961878,0.0043322197,0.00018281251,0.00087999913,0.9600399,0.000282623,0.0015204094,0.000021256908],"about_ca_topic_score_codex":0.0014193782,"about_ca_topic_score_gemma":0.0022382236,"teacher_disagreement_score":0.002815578,"about_ca_system_score_codex":0.00039205205,"about_ca_system_score_gemma":0.00033259633,"threshold_uncertainty_score":0.009419024},"labels":[],"label_agreement":null}]}