{"meta":{"query_hash":"b812a16aea51","filters":{"venue":"Human Heredity"},"cohort_total":42,"direct_labels_cover":0,"predictions_cover":42,"exported":42,"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/b812a16aea51","api":"https://metacan.xera.ac/api/v1/cohort?venue=Human+Heredity"},"results":[{"id":"W1964401457","doi":"10.1159/000341392","title":"Detection of Phenotype Modifier Genes Using Two-Locus Linkage Analysis in Complex Disorders Such as Major Psychosis","year":2012,"lang":"en","type":"article","venue":"Human Heredity","topic":"Genetic Associations and Epidemiology","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":true,"ca_institutions":"Université Laval; Institut Universitaire en Santé Mentale de Québec","funders":"Canadian Institutes of Health Research; Université Laval","keywords":"Phenotype; Psychosis; Locus (genetics); Genetics; Genetic linkage; Gene; Biology; Linkage (software); Psychology; Psychiatry","score_opus":0.0416173938250767,"score_gpt":0.33400348964765675,"score_spread":0.29238609582258007,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1964401457","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9926056,0.0005736133,0.0059732865,0.00002604921,0.00013157891,0.000105338644,0.000015880114,0.000006171999,0.00056246715],"genre_scores_gemma":[0.99863684,0.000059525824,0.00076868053,0.000042817304,0.00029463213,0.000010718861,0.000115062394,0.000012042282,0.00005967021],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9989282,0.00017663237,0.00030597002,0.00022617752,0.0000866109,0.00027643063],"domain_scores_gemma":[0.99941486,0.000017450355,0.00017333135,0.00027773977,0.00005528747,0.00006131076],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00039188322,0.00012158237,0.00025197832,0.00010883417,0.000097721066,0.000005396015,0.000106003215,0.00017021479,0.00009923077],"category_scores_gemma":[0.000059591457,0.00012511268,0.00014949354,0.00024951418,0.000066099456,0.000004672974,0.000051177765,0.00007915477,0.0000051319867],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.000018002966,0.00013888153,0.63503927,0.0000097841785,0.00021410671,9.729499e-8,0.00008036099,0.001695202,0.36111635,0.000035442637,0.00007797103,0.0015745276],"study_design_scores_gemma":[0.0005378249,0.000095074494,0.98443234,0.000002662831,0.00022855392,9.3314515e-7,0.00010812079,0.001703568,0.011333664,0.00048242614,0.00087632955,0.00019847341],"about_ca_topic_score_codex":0.0025803393,"about_ca_topic_score_gemma":0.0049578017,"teacher_disagreement_score":0.3497827,"about_ca_system_score_codex":0.00003004049,"about_ca_system_score_gemma":0.000013671571,"threshold_uncertainty_score":0.5101947},"labels":[],"label_agreement":null},{"id":"W1965771219","doi":"10.1159/000363443","title":"Using Gene Genealogies to Detect Rare Variants Associated with Complex Traits","year":2014,"lang":"en","type":"article","venue":"Human Heredity","topic":"Genetic Associations and Epidemiology","field":"Biochemistry, Genetics and Molecular Biology","cited_by":6,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Simon Fraser University; McGill University; Jewish General Hospital; University of Ottawa","funders":"Natural Sciences and Engineering Research Council of Canada; Canadian Institutes of Health Research","keywords":"Biology; Tree (set theory); Statistic; Population; Genetics; Haplotype; Genetic association; Genetic variation; Evolutionary biology; Computational biology; Gene; Statistics; Allele; Single-nucleotide polymorphism; Genotype; Mathematics; Medicine","score_opus":0.08093057822295222,"score_gpt":0.3092738918425877,"score_spread":0.22834331361963547,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1965771219","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9709348,0.000035487657,0.02779458,0.00006643636,0.000084359526,0.0001655999,0.000055351098,0.000029750056,0.00083365134],"genre_scores_gemma":[0.9874981,0.0000035689209,0.01122189,0.0004734485,0.00039996233,0.000013940932,0.00020048699,0.000025015943,0.0001635913],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9986712,0.00024697836,0.00022685915,0.00037868856,0.000112415415,0.0003638593],"domain_scores_gemma":[0.99932337,0.000034564237,0.00013197685,0.00026735806,0.0001290258,0.0001137362],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00040876862,0.00017281967,0.00025620876,0.000035306766,0.00026269467,0.000020643263,0.00019301452,0.00019487011,0.000053178315],"category_scores_gemma":[0.00041024614,0.00015660771,0.000062537394,0.00009243335,0.00006279978,0.000002433444,0.00009876548,0.000081678,0.00000950738],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.000046675756,0.00008211132,0.04326755,0.000011368035,0.00022354965,0.000004668659,0.00011611698,0.0032056414,0.9394374,0.00006850087,0.010294171,0.0032422752],"study_design_scores_gemma":[0.0006563072,0.000542433,0.9870962,0.000011247177,0.000040780134,0.000011753207,0.000025750802,0.0006293882,0.006136119,0.00051599037,0.0040281625,0.00030589147],"about_ca_topic_score_codex":0.000069401016,"about_ca_topic_score_gemma":0.00053970836,"teacher_disagreement_score":0.94382864,"about_ca_system_score_codex":0.00003991554,"about_ca_system_score_gemma":0.0000444318,"threshold_uncertainty_score":0.6386277},"labels":[],"label_agreement":null},{"id":"W1967425407","doi":"10.1159/000346478","title":"Rare Variants in Complex Traits: Novel Identification Strategies and the Role of de novo Mutations","year":2012,"lang":"en","type":"article","venue":"Human Heredity","topic":"Genomic variations and chromosomal abnormalities","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":"Centre Hospitalier de l’Université de Montréal; Centre Hospitalier Universitaire Sainte-Justine; Université de Montréal","funders":"","keywords":"Genetics; Biology; Identification (biology); Phenotype; Mutation; Computational biology; Evolutionary biology; Gene","score_opus":0.022120373148008663,"score_gpt":0.25753243416318267,"score_spread":0.235412061015174,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1967425407","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99757373,0.00026156078,0.00074800785,0.00003155719,0.000023097135,0.000093067174,0.00005644226,0.000003052034,0.001209489],"genre_scores_gemma":[0.9993995,0.000008447445,0.00026515574,0.000015917567,0.00012441598,0.000017713135,0.00011429482,0.0000044523485,0.000050104492],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9995774,0.000043961576,0.00015417924,0.00007591538,0.000041759486,0.00010679339],"domain_scores_gemma":[0.9997726,0.000011048335,0.00006296419,0.00009873554,0.0000329092,0.000021758211],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00020764848,0.000052308787,0.00006905633,0.000016414118,0.00008263123,0.000025785406,0.00007181936,0.000045774043,0.00003380551],"category_scores_gemma":[0.000018254847,0.00004337105,0.00002188972,0.000031792846,0.000109898196,0.000013709777,0.000028899052,0.000036416495,8.236624e-7],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.000027703149,0.00014265487,0.023208203,0.000023746616,0.000026340624,1.4338744e-7,0.0028057494,0.000073797346,0.9017506,0.071616724,0.000048987313,0.00027530466],"study_design_scores_gemma":[0.0009842657,0.000024592879,0.9642151,0.000005107075,0.000019397196,0.000020715715,0.007855923,0.000095896634,0.021450646,0.0043736678,0.00086603995,0.00008866409],"about_ca_topic_score_codex":0.0001322128,"about_ca_topic_score_gemma":0.0001829327,"teacher_disagreement_score":0.9410069,"about_ca_system_score_codex":0.0000075637895,"about_ca_system_score_gemma":0.000034034347,"threshold_uncertainty_score":0.176862},"labels":[],"label_agreement":null},{"id":"W1970115933","doi":"10.1159/000070665","title":"Fine Mapping of the Schizophrenia Susceptibility Locus on Chromosome 1q22","year":2002,"lang":"en","type":"article","venue":"Human Heredity","topic":"Genetic Associations and Epidemiology","field":"Biochemistry, Genetics and Molecular Biology","cited_by":43,"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 Toronto; Centre for Addiction and Mental Health","funders":"National Institute of Mental Health; Health Canada; National Institutes of Health; Canadian Institutes of Health Research; National Institute for Health and Care Research; National Human Genome Research Institute; National Alliance for Research on Schizophrenia and Depression; Johns Hopkins University","keywords":"Locus (genetics); Genetics; Gene duplication; Genetic linkage; Biology; Schizoaffective disorder; Gene mapping; Population; Segmental duplication; Gene; Human genome; Candidate gene; Psychosis; Gene map; Genome; Chromosome; Gene family; Medicine; Psychiatry","score_opus":0.03518192598605137,"score_gpt":0.2575742806765708,"score_spread":0.22239235469051943,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1970115933","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9961382,0.00017640392,0.000044786528,0.00030498652,0.00021693125,0.000127644,0.000029305827,0.000008308498,0.0029534083],"genre_scores_gemma":[0.9981731,0.000014072948,0.00012654002,0.0001072609,0.00041993626,0.000007877871,0.000022415848,0.000009206118,0.0011195823],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9990381,0.00014956621,0.0002544517,0.00026267546,0.00010221866,0.00019297929],"domain_scores_gemma":[0.99917054,0.000023128074,0.00015000162,0.0005557104,0.000060499555,0.000040129657],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0002629913,0.000110962894,0.00016539637,0.000017314285,0.00015705625,0.0000048259926,0.00022863397,0.00014813672,0.00039423042],"category_scores_gemma":[0.00023137763,0.00008406965,0.00012773274,0.000075971744,0.00013783816,0.0000012602957,0.000115512485,0.00012260713,0.000024193396],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.000037684877,0.0005193457,0.270233,0.000056096596,0.00012642513,0.0000016510759,0.00016703384,0.00032355587,0.6146613,0.00047513063,0.10855972,0.0048390543],"study_design_scores_gemma":[0.0010132384,0.00044512228,0.9482048,0.00002705428,0.000022010212,0.0000056902522,0.000044352615,0.00014504697,0.029284436,0.0010678893,0.019473013,0.0002673413],"about_ca_topic_score_codex":0.0000378052,"about_ca_topic_score_gemma":0.0002825433,"teacher_disagreement_score":0.6779718,"about_ca_system_score_codex":0.000021215885,"about_ca_system_score_gemma":0.000014141179,"threshold_uncertainty_score":0.43165466},"labels":[],"label_agreement":null},{"id":"W1977673229","doi":"10.1159/000336293","title":"A Unified Framework for Detecting Rare Variant Quantitative Trait Associations in Pedigree and Unrelated Individuals via Sequence Data","year":2012,"lang":"en","type":"article","venue":"Human Heredity","topic":"Genetic Associations and Epidemiology","field":"Biochemistry, Genetics and Molecular Biology","cited_by":15,"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; National Heart, Lung, and Blood Institute; National Institute on Minority Health and Health Disparities; Canadian Institutes of Health Research; Rice University; National Institutes of Health; National Science Foundation","keywords":"Trait; Genetics; Biology; Population; Computer science; Medicine","score_opus":0.15889297931324814,"score_gpt":0.3856703577677539,"score_spread":0.22677737845450574,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1977673229","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.95141727,0.00041351904,0.046745725,0.00016257096,0.00016781331,0.00030574156,0.00067717535,0.000013441454,0.000096732845],"genre_scores_gemma":[0.9658256,0.000024175595,0.03246639,0.00010734441,0.00028195357,0.000036681195,0.0012066367,0.000014821706,0.00003638556],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99871886,0.00022461172,0.00030546432,0.0003234806,0.000073873656,0.00035370165],"domain_scores_gemma":[0.99897075,0.00032834764,0.00021661489,0.00033509833,0.000070903705,0.00007830124],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0013612137,0.00012648666,0.0002080796,0.000041245024,0.00021961522,0.00001728187,0.00020618693,0.0003406363,0.000016186834],"category_scores_gemma":[0.0024922881,0.00013137308,0.00003492158,0.00010175168,0.00005729059,0.0000145503045,0.00016820787,0.00018958056,0.0000014684074],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.000031845186,0.000256053,0.9573674,0.000047296722,0.00030545183,0.0000021056583,0.0024447017,0.000094288516,0.026059747,0.009034162,0.0022271753,0.0021297734],"study_design_scores_gemma":[0.00076075154,0.00022866899,0.98004484,0.000026808404,0.00007692375,0.000010291054,0.00058624864,0.0011304491,0.00036699005,0.015048276,0.0014060887,0.00031367343],"about_ca_topic_score_codex":0.0001758672,"about_ca_topic_score_gemma":0.000511957,"teacher_disagreement_score":0.025692755,"about_ca_system_score_codex":0.000036979927,"about_ca_system_score_gemma":0.000047180827,"threshold_uncertainty_score":0.53572387},"labels":[],"label_agreement":null},{"id":"W1984147133","doi":"10.1159/000096096","title":"Locus-Specific Heritability Estimation via the Bootstrap in Linkage Scans for Quantitative Trait Loci","year":2006,"lang":"en","type":"article","venue":"Human Heredity","topic":"Genetic Associations and Epidemiology","field":"Biochemistry, Genetics and Molecular Biology","cited_by":17,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Toronto; Lunenfeld-Tanenbaum Research Institute; Mount Sinai Hospital","funders":"Canadian Institutes of Health Research; School of Medicine, Boston University","keywords":"Heritability; Quantitative trait locus; Genetics; Trait; Locus (genetics); Biology; Linkage (software); Genetic linkage; Genetic architecture; Evolutionary biology; Computational biology; Gene; Computer science","score_opus":0.04448857699598985,"score_gpt":0.3186760453409089,"score_spread":0.274187468344919,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1984147133","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.91831344,0.00036081416,0.07968352,0.00041262046,0.00011204047,0.0004263144,0.00007685554,0.000011777666,0.00060262735],"genre_scores_gemma":[0.9955073,0.0000118706375,0.0033878833,0.00006783743,0.0003050261,0.0000971577,0.00042513834,0.000013305612,0.00018450207],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.998847,0.0001663015,0.0003424052,0.0003153413,0.00007330317,0.000255615],"domain_scores_gemma":[0.9993801,0.000107580534,0.00012324577,0.00027570882,0.00008551801,0.000027840697],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00069935125,0.0001284977,0.00017226386,0.00002195316,0.0001892317,0.000017103295,0.00015417048,0.0001823072,0.00003781926],"category_scores_gemma":[0.00013226227,0.00010758481,0.000106735744,0.00007156397,0.00015738343,0.0000040596874,0.00002973003,0.00010760005,0.0000047958356],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00049472385,0.0023734167,0.31658432,0.00030217806,0.0002679929,0.000008066964,0.0016033524,0.100316264,0.3838268,0.026650142,0.1439529,0.023619857],"study_design_scores_gemma":[0.0010069715,0.00040245202,0.9482963,0.00000858985,0.00001858338,0.0000025973602,0.0002793493,0.0065316604,0.0022781396,0.026574936,0.014307872,0.00029253928],"about_ca_topic_score_codex":0.0003440506,"about_ca_topic_score_gemma":0.0026882468,"teacher_disagreement_score":0.631712,"about_ca_system_score_codex":0.000043962027,"about_ca_system_score_gemma":0.000031537864,"threshold_uncertainty_score":0.4387181},"labels":[],"label_agreement":null},{"id":"W1995154596","doi":"10.1159/000101964","title":"Campora: A Young Genetic Isolate in South Italy","year":2007,"lang":"en","type":"article","venue":"Human Heredity","topic":"Yersinia bacterium, plague, ectoparasites research","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":"Polytechnique Montréal","funders":"Associazione Italiana per la Ricerca sul Cancro; Regione Campania","keywords":"Biology; Genetics; Haplotype; Linkage disequilibrium; Population; Evolutionary biology; Locus (genetics); Autosome; Mitochondrial DNA; Population bottleneck; Population genetics; Genotype; Chromosome; Allele; Microsatellite; Gene; Demography","score_opus":0.017856873233322804,"score_gpt":0.2991607572688282,"score_spread":0.2813038840355054,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1995154596","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99541146,0.00024530955,0.00029179556,0.000014847646,0.0001669965,0.00021432686,0.00001976938,0.00001891535,0.0036166036],"genre_scores_gemma":[0.99809045,0.00000808327,0.00028359267,0.000051440427,0.0004935221,0.000008829838,0.00009020696,0.000029443067,0.00094440934],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9984659,0.000062944884,0.00028928908,0.00044157085,0.00020164576,0.00053867727],"domain_scores_gemma":[0.99925643,0.000011830621,0.00006966792,0.00044194146,0.00007324654,0.00014687756],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0004579011,0.00017349652,0.00016665854,0.00010787642,0.00009511665,0.00003930802,0.00026656687,0.00020875757,0.00012792907],"category_scores_gemma":[0.00007173463,0.00018414985,0.00007663586,0.00015160964,0.00010812308,0.000005331914,0.00015576599,0.00022854016,0.000081016515],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.000095922354,0.00008145491,0.42053273,0.000023353772,0.000016904758,0.00010027351,0.00031640663,0.000007630674,0.57807195,0.000008046925,0.0005142131,0.00023111854],"study_design_scores_gemma":[0.00072631455,0.00024190142,0.9570875,0.000010767756,0.00000689494,0.00003778872,0.00013361473,0.000025368343,0.039241154,0.000047196438,0.0021747134,0.00026674676],"about_ca_topic_score_codex":0.00015400143,"about_ca_topic_score_gemma":0.002142037,"teacher_disagreement_score":0.5388308,"about_ca_system_score_codex":0.000053219675,"about_ca_system_score_gemma":0.00006438966,"threshold_uncertainty_score":0.7509413},"labels":[],"label_agreement":null},{"id":"W1999593164","doi":"10.1159/000077385","title":"Examination of Potential Overlap in Autism and Language Loci on Chromosomes 2, 7, and 13 in Two Independent Samples Ascertained for Specific Language Impairment","year":2004,"lang":"en","type":"article","venue":"Human Heredity","topic":"Autism Spectrum Disorder Research","field":"Neuroscience","cited_by":101,"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 Institute on Deafness and Other Communication Disorders; National Institute of Mental Health; National Institutes of Health","keywords":"Autism; Genetic linkage; Genetics; Linkage (software); FOXP2; Biology; Specific language impairment; Chromosome; Heritability of autism; Neurodevelopmental disorder; Autism spectrum disorder; Psychology; Developmental psychology; Gene","score_opus":0.03175441174563211,"score_gpt":0.32315320801883063,"score_spread":0.29139879627319853,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1999593164","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99832183,0.00019500541,0.000064239626,0.00031493057,0.000054137286,0.0007321922,0.00006392804,0.00002552764,0.00022818519],"genre_scores_gemma":[0.99967873,0.00004857718,0.000056530767,0.000024757006,0.000052147814,0.00004156287,0.00002078315,0.000017708891,0.00005920839],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9985217,0.00012960748,0.0002462372,0.00042988523,0.0003639418,0.00030862156],"domain_scores_gemma":[0.99955577,0.000099509634,0.00007980951,0.00019872408,0.000005038655,0.00006118117],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00038894336,0.00014067389,0.00020910379,0.00026116645,0.00008273514,0.00004326685,0.00014060405,0.000060100665,0.00008015217],"category_scores_gemma":[0.000084735955,0.0001410556,0.00003038936,0.00016493308,0.00012776458,0.0001374135,0.000105617415,0.00020382807,0.000003048728],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0005705532,0.0033019078,0.042907827,0.00068474305,0.000019391386,0.00085791433,0.04625052,0.0010712397,0.7488232,0.13343173,0.000095174546,0.02198579],"study_design_scores_gemma":[0.004682954,0.00043422502,0.94064814,0.000061391016,0.0000028871511,0.000012361769,0.0010539757,0.0002607603,0.046427906,0.006236944,0.000013905633,0.00016456886],"about_ca_topic_score_codex":0.0014947259,"about_ca_topic_score_gemma":0.0053090914,"teacher_disagreement_score":0.8977403,"about_ca_system_score_codex":0.00018732413,"about_ca_system_score_gemma":0.00003171231,"threshold_uncertainty_score":0.575208},"labels":[],"label_agreement":null},{"id":"W2002284887","doi":"10.1159/000053364","title":"Haplotype Analysis of <i>BRCA2</i> 8765delAG Mutation Carriers in French Canadian and Yemenite Jewish Hereditary Breast Cancer Families","year":2001,"lang":"en","type":"article","venue":"Human Heredity","topic":"BRCA gene mutations in cancer","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":true,"ca_institutions":"Jewish General Hospital; Centre Hospitalier de l’Université de Montréal; McGill University; Université de Montréal; Women's College Hospital; Hôpital Notre-Dame; McGill University Health Centre","funders":"","keywords":"Haplotype; Genetics; Allele; Microsatellite; Mutation; Biology; Identity by descent; BRCA2 Protein; Germline mutation; Gene","score_opus":0.011939264425029034,"score_gpt":0.25751816079049117,"score_spread":0.24557889636546212,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2002284887","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99378663,0.0031969976,0.000042018874,0.00019974026,0.00028823773,0.000181875,0.00079589745,0.000013150252,0.0014954272],"genre_scores_gemma":[0.99791676,0.00038821084,0.00011797087,0.00012293544,0.00034259728,0.000057283505,0.00066948525,0.000027199572,0.00035754498],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9985307,0.00008267023,0.0003598567,0.000475889,0.0002066119,0.00034428376],"domain_scores_gemma":[0.99906194,0.000015207985,0.00012933083,0.00038946822,0.00022183034,0.00018219792],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00020686074,0.00020852155,0.00029254504,0.00041942447,0.00014975778,0.000024292032,0.00018798765,0.00022475666,0.0003448281],"category_scores_gemma":[0.000032234973,0.00023812681,0.0000891976,0.0006927093,0.00023392131,0.00001753986,0.000059856444,0.00011594575,0.000002133008],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":true,"about_ca_topic_consensus":true,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00014086987,0.0002151139,0.7282358,0.00015486017,0.0027531863,0.00016362777,0.0028915955,0.014346097,0.19239923,0.00022934389,0.03052598,0.027944315],"study_design_scores_gemma":[0.0007711248,0.00010957508,0.9774639,0.00002340821,0.00045647303,0.000026291389,0.00024702193,0.0010079197,0.001550407,0.00018873703,0.017770102,0.0003850639],"about_ca_topic_score_codex":0.05477065,"about_ca_topic_score_gemma":0.86666185,"teacher_disagreement_score":0.8118912,"about_ca_system_score_codex":0.00028212566,"about_ca_system_score_gemma":0.00046334427,"threshold_uncertainty_score":0.971053},"labels":[],"label_agreement":null},{"id":"W2010459055","doi":"10.1159/000096035","title":"A Posterior Probability of Linkage-Based Re-Analysis of Schizophrenia Data Yields Evidence of Linkage to Chromosomes 1 and 17","year":2006,"lang":"en","type":"article","venue":"Human Heredity","topic":"Genetic Associations and Epidemiology","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 for Addiction and Mental Health","funders":"National Human Genome Research Institute; National Institute of Mental Health; U.S. Public Health Service","keywords":"Linkage (software); Genetic linkage; Lod score; Genetics; Chromosome; Pedigree chart; Bayesian probability; Computational biology; Biology; Mathematics; Computer science; Gene; Gene mapping; Statistics","score_opus":0.06723230674384337,"score_gpt":0.3277766037798121,"score_spread":0.2605442970359687,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2010459055","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9979829,0.00060341856,0.00059504993,0.00017708131,0.0000305638,0.00019772381,0.0003417528,0.0000043593695,0.00006714971],"genre_scores_gemma":[0.99422807,0.000020126572,0.005232494,0.000045985453,0.0000963203,0.0000082954075,0.00029841097,0.0000067475307,0.000063580774],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99856216,0.0001697407,0.00057736854,0.0004135819,0.00012580765,0.00015132967],"domain_scores_gemma":[0.9982564,0.00011163193,0.00036674738,0.0010156706,0.00019964259,0.00004991977],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0008121117,0.00012042895,0.0004871058,0.000082764665,0.000045095156,0.000005142846,0.0003368674,0.00019383196,0.000053196614],"category_scores_gemma":[0.00062321214,0.00011335974,0.00011978933,0.00021862797,0.00017417787,0.000004942066,0.0002877149,0.00006856324,3.988209e-7],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00013824443,0.00023347321,0.52312154,0.00024862704,0.00038246406,7.4562894e-7,0.00005088483,0.0010663951,0.47210988,0.000023091428,0.0021309168,0.000493732],"study_design_scores_gemma":[0.00034947932,0.0005312175,0.9667395,0.00006522659,0.0004835083,5.043158e-7,0.000026583533,0.00063981727,0.030708008,0.00017854042,0.00013790208,0.00013976192],"about_ca_topic_score_codex":0.00065523176,"about_ca_topic_score_gemma":0.0021727108,"teacher_disagreement_score":0.4436179,"about_ca_system_score_codex":0.000010376343,"about_ca_system_score_gemma":0.000083179584,"threshold_uncertainty_score":0.4622676},"labels":[],"label_agreement":null},{"id":"W2013110935","doi":"10.1159/000331463","title":"Using Parametric Multipoint Lods and Mods for Linkage Analysis Requires a Shift in Statistical Thinking","year":2011,"lang":"en","type":"article","venue":"Human Heredity","topic":"Genetic Mapping and Diversity in Plants and Animals","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":"Institute for Clinical Evaluative Sciences; SickKids Foundation; Hospital for Sick Children","funders":"National Human Genome Research Institute; National Institute of Mental Health","keywords":"Linkage (software); Statistics; Permutation (music); Statistical hypothesis testing; Mathematics; Computer science; Genetics; Biology","score_opus":0.12627566242342403,"score_gpt":0.32948203117939817,"score_spread":0.20320636875597414,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2013110935","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9608101,0.00014813179,0.038452186,0.0000051404804,0.000042085067,0.000118678814,0.00008771907,0.000007138884,0.00032880087],"genre_scores_gemma":[0.9859531,0.000017571982,0.01378996,0.000039874216,0.0000849697,0.0000042443544,0.00007285299,0.000005359434,0.000032044543],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9992554,0.000041957985,0.00016267202,0.00027795043,0.00007565254,0.00018632412],"domain_scores_gemma":[0.9996895,0.000025461253,0.00005466985,0.00013992061,0.000026370073,0.00006407001],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00027259282,0.00010021669,0.00017000303,0.0001129671,0.00013148646,0.000027241542,0.00009514085,0.000109770044,0.00004230088],"category_scores_gemma":[0.00007865577,0.00009594937,0.000062193074,0.0001094511,0.00006762912,0.0000031258053,0.000087984445,0.000059514376,5.640609e-7],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00038982343,0.000652835,0.9418958,0.00032642178,0.0008370991,0.000064034015,0.0025614037,0.00066921057,0.043793462,0.005371175,0.0009906864,0.0024480887],"study_design_scores_gemma":[0.001794813,0.0007272936,0.9678612,0.000048239664,0.00048816288,0.000008420403,0.00052967283,0.011786247,0.005748769,0.009406844,0.00098546,0.00061491714],"about_ca_topic_score_codex":0.0003472616,"about_ca_topic_score_gemma":0.00024841743,"teacher_disagreement_score":0.038044695,"about_ca_system_score_codex":0.0000072830735,"about_ca_system_score_gemma":0.0000152250805,"threshold_uncertainty_score":0.3912702},"labels":[],"label_agreement":null},{"id":"W2013643587","doi":"10.1159/000343751","title":"Intra-Familial Tests of Association between Familial Idiopathic Scoliosis and Linked Regions on 9q31.3–q34.3 and 16p12.3–q22.2","year":2012,"lang":"en","type":"article","venue":"Human Heredity","topic":"Scoliosis diagnosis and treatment","field":"Medicine","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; Centre Hospitalier Universitaire Sainte-Justine","funders":"National Center for Research Resources; National Institute of Arthritis and Musculoskeletal and Skin Diseases; National Human Genome Research Institute","keywords":"Candidate gene; Genetics; Genotyping; Genetic linkage; Single-nucleotide polymorphism; Biology; Genetic association; Linkage (software); Gene; Genotype","score_opus":0.0592566999348315,"score_gpt":0.3188777373254492,"score_spread":0.2596210373906177,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2013643587","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9968771,0.0008951322,0.0000028334182,0.00062982,0.0002843952,0.0005331325,0.00003961256,0.000058973994,0.00067905424],"genre_scores_gemma":[0.9975164,0.00029854538,0.000047474205,0.00020192974,0.0017559332,0.000058427067,0.000022022483,0.00002603009,0.0000732443],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9983671,0.00012890976,0.00040127532,0.00030727527,0.000423576,0.00037189646],"domain_scores_gemma":[0.9988657,0.00017551925,0.00024152629,0.00028946353,0.000121338286,0.00030640428],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00057003327,0.00022868291,0.00057090895,0.00014812643,0.00019674934,0.000023029233,0.00005633724,0.00027322807,0.000019663343],"category_scores_gemma":[0.0003986274,0.00018334022,0.00010122593,0.00016103341,0.000113108,0.00013644682,0.000059127677,0.00027859482,0.000014318975],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00005146094,0.0006548459,0.9939572,0.0001309929,0.00018634224,0.00000488348,0.00059174374,1.213493e-7,0.0009367564,0.00048074854,0.0015816238,0.0014232416],"study_design_scores_gemma":[0.002189015,0.00086318626,0.99269855,0.00062444556,0.00055769185,0.000005633094,0.00008942569,0.0000030714077,0.0022437652,0.0002762901,0.0002915612,0.00015735674],"about_ca_topic_score_codex":0.00028744325,"about_ca_topic_score_gemma":0.00012368312,"teacher_disagreement_score":0.002137554,"about_ca_system_score_codex":0.00028205803,"about_ca_system_score_gemma":0.000051629107,"threshold_uncertainty_score":0.7476397},"labels":[],"label_agreement":null},{"id":"W2014348387","doi":"10.1159/000224636","title":"Genome Scan, Fine-Mapping, and Candidate Gene Analysis of Non-Syndromic Cleft Lip with or without Cleft Palate Reveals Phenotype-Specific Differences in Linkage and Association Results","year":2009,"lang":"en","type":"article","venue":"Human Heredity","topic":"Cleft Lip and Palate Research","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":"Children's & Women's Health Centre of British Columbia; BC Research (Canada); University of British Columbia","funders":"National Center for Research Resources; National Institute of Dental and Craniofacial Research; March of Dimes Foundation; National Institutes of Health; National Human Genome Research Institute; Johns Hopkins University; Hope Foundation","keywords":"Candidate gene; Genetics; Single-nucleotide polymorphism; Genome-wide association study; Phenotype; Genetic linkage; Genome; Genetic association; Linkage (software); Biology; Gene; Genotype","score_opus":0.02629556798395929,"score_gpt":0.2794754490371429,"score_spread":0.2531798810531836,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2014348387","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99908537,0.000106689135,0.000040713192,0.00007241405,0.00002359849,0.00021885599,0.00011868706,0.000007236386,0.00032646634],"genre_scores_gemma":[0.9978871,0.0009113827,0.00012779399,0.000023179808,0.0001823785,0.000004659254,0.00023774178,0.000010826393,0.0006149494],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9985373,0.00011139387,0.00037372397,0.0004664061,0.00021411238,0.0002970555],"domain_scores_gemma":[0.9991998,0.0000359377,0.00022982628,0.00030551388,0.00012038276,0.000108529566],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0005430648,0.00017680488,0.00044857964,0.00018560482,0.00011332164,0.00004877028,0.00013007186,0.00019064789,0.000025787695],"category_scores_gemma":[0.000048584312,0.00014103026,0.000048291757,0.00031454777,0.000103273895,0.0000088354445,0.00006236052,0.00016741846,0.0000010404865],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00023644204,0.000055524226,0.7991121,0.000025268851,0.00020380103,0.00000782288,0.00035613737,0.000010498616,0.19936348,0.0000025406232,0.00007750202,0.00054887385],"study_design_scores_gemma":[0.001120065,0.0004617843,0.9964888,0.000037625327,0.00007940227,0.0000030503386,0.000039001476,0.00021740812,0.001088203,0.000026210562,0.00025330708,0.00018514908],"about_ca_topic_score_codex":0.00025239395,"about_ca_topic_score_gemma":0.004918541,"teacher_disagreement_score":0.19827528,"about_ca_system_score_codex":0.00003846903,"about_ca_system_score_gemma":0.000046771194,"threshold_uncertainty_score":0.5751048},"labels":[],"label_agreement":null},{"id":"W2020675161","doi":"10.1159/000330780","title":"Causal Models for Investigating Complex Genetic Disease: II. What Causal Models Can Tell Us about Penetrance for Additive, Heterogeneity, and Multiplicative Two-Locus Models","year":2011,"lang":"en","type":"article","venue":"Human Heredity","topic":"Genetic Associations and Epidemiology","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":"Columbia College","funders":"National Institute of Neurological Disorders and Stroke; National Institute of Mental Health; National Institutes of Health","keywords":"Penetrance; Locus (genetics); Additive model; Multiplicative function; Genetic model; Genetics; Causal model; Biology; Econometrics; Mathematics; Gene; Statistics; Phenotype","score_opus":0.11654759684130037,"score_gpt":0.320852887372162,"score_spread":0.20430529053086163,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2020675161","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9171363,0.0016275827,0.07799735,0.00006643594,0.00014319194,0.0012675353,0.0015552827,0.00003198526,0.00017431138],"genre_scores_gemma":[0.973615,0.00040761108,0.023034811,0.00043319174,0.0004650987,0.00078527967,0.0010736275,0.00006709516,0.00011827564],"study_design_codex":"simulation_or_modeling","study_design_gemma":"simulation_or_modeling","domain_scores_codex":[0.997602,0.0001385425,0.0005261295,0.0009367207,0.00014250583,0.0006541083],"domain_scores_gemma":[0.99836373,0.000080470185,0.00031759476,0.0005182898,0.00034338492,0.00037650095],"candidate_categories":["metaepi_narrow"],"consensus_categories":[],"category_scores_codex":[0.00030443817,0.00039208055,0.0004678487,0.000047171303,0.00066683366,0.000051077866,0.00030774198,0.00024938138,0.000010674039],"category_scores_gemma":[0.00008600583,0.0004105268,0.0001827482,0.000053953543,0.0003656387,0.000041484713,0.000250416,0.00013127094,7.11394e-7],"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":[0.001969133,0.0025421355,0.12699899,0.0012946161,0.002840795,0.000023418934,0.008916085,0.58087415,0.20569447,0.02110074,0.026429992,0.021315465],"study_design_scores_gemma":[0.004294476,0.0011567994,0.13889165,0.00010449003,0.00030734492,0.00001606592,0.00026811997,0.7288073,0.00970903,0.11413345,0.00091860234,0.0013926731],"about_ca_topic_score_codex":0.00044123933,"about_ca_topic_score_gemma":0.0019806542,"teacher_disagreement_score":0.19598544,"about_ca_system_score_codex":0.000052549105,"about_ca_system_score_gemma":0.000129946,"threshold_uncertainty_score":0.99983466},"labels":[],"label_agreement":null},{"id":"W2022048405","doi":"10.1159/000053379","title":"The Null Distribution of the Heterogeneity Lod Score Does Depend on the Assumed Genetic Model for the Trait","year":2001,"lang":"en","type":"article","venue":"Human Heredity","topic":"Genetic Mapping and Diversity in Plants and Animals","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":"Actua","funders":"U.S. Public Health Service","keywords":"Locus (genetics); Genetics; Biology; Gene","score_opus":0.04397627985118423,"score_gpt":0.25742137998237735,"score_spread":0.2134451001311931,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2022048405","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99591595,0.00019213458,0.0018219955,0.0008912775,0.00019351412,0.00037555236,0.000391304,0.0000056044632,0.0002126804],"genre_scores_gemma":[0.9986374,0.00014734712,0.000015382519,0.00017692921,0.00024987943,0.0000248091,0.00005260996,0.0000065332897,0.00068913813],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.999176,0.00007829882,0.00015931691,0.00020272513,0.0001710238,0.00021258487],"domain_scores_gemma":[0.9992104,0.000085050284,0.00010941247,0.0004878231,0.000074761774,0.00003255282],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00031204202,0.0001247941,0.00009105236,0.0000040827576,0.0009864332,0.000045105564,0.00052897516,0.00008738466,0.000014428861],"category_scores_gemma":[0.00008438904,0.000047726062,0.00017399008,0.00003476987,0.00018288045,0.0000015531061,0.000115191,0.0000955448,0.0000013737213],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0020282378,0.0016667425,0.12874465,0.00030022848,0.0018016923,0.0000103844195,0.0014643414,0.029151846,0.4884533,0.018646214,0.30452377,0.02320861],"study_design_scores_gemma":[0.0025309043,0.00097252696,0.59867674,0.000109562985,0.00045697956,0.00005119534,0.0010602825,0.025753576,0.18151605,0.009597835,0.1784181,0.0008562632],"about_ca_topic_score_codex":0.0000443515,"about_ca_topic_score_gemma":0.0006337592,"teacher_disagreement_score":0.46993208,"about_ca_system_score_codex":0.000008611208,"about_ca_system_score_gemma":0.00003195437,"threshold_uncertainty_score":0.7586947},"labels":[],"label_agreement":null},{"id":"W2029909776","doi":"10.1159/000345604","title":"Cumulative Meta-Analysis for Genetic Association: When Is a New Study Worthwhile?","year":2012,"lang":"en","type":"article","venue":"Human Heredity","topic":"Genetic Associations and Epidemiology","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":"Lunenfeld-Tanenbaum Research Institute; University of Toronto; York University; Mount Sinai Hospital","funders":"Canadian Institutes of Health Research","keywords":"Meta-analysis; Single-nucleotide polymorphism; SNP; Genetic association; Genetics; Context (archaeology); Genome-wide association study; Trait; Biology; Sample size determination; Genotype; Statistics; Medicine; Gene; Mathematics; Computer science; Internal medicine","score_opus":0.14837127351587195,"score_gpt":0.3618152803059576,"score_spread":0.21344400679008566,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2029909776","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9866036,0.0017162929,0.0093682045,0.00059354055,0.00021335705,0.0007868629,0.00013581965,0.00001976455,0.00056256313],"genre_scores_gemma":[0.9786838,0.000008982171,0.0045579067,0.0005539321,0.001246545,0.0001653553,0.00017922475,0.000020115907,0.014584136],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99826616,0.00027240964,0.00042429141,0.00040589305,0.0001899837,0.00044125374],"domain_scores_gemma":[0.9987234,0.000091764574,0.00035356855,0.00047519925,0.00018511618,0.00017095472],"candidate_categories":["insufficient_payload"],"consensus_categories":[],"category_scores_codex":[0.00095484644,0.00020391056,0.00063195714,0.000062793726,0.00022231537,0.00002336032,0.0001839987,0.00022409247,0.0010057758],"category_scores_gemma":[0.00027015666,0.00018389935,0.0008571673,0.00014531202,0.000019790918,0.0000058091387,0.00009002659,0.000088321256,0.000025208048],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.000010684108,0.00027816233,0.860619,0.0000032346043,0.05524486,1.8009514e-7,0.0010576879,0.00014284745,0.00020931156,0.000027135615,0.08227362,0.00013324726],"study_design_scores_gemma":[0.0006915564,0.0003337785,0.8929478,2.6146637e-7,0.05210411,6.342384e-7,0.00026187024,0.00004365851,0.00020858005,0.0015244376,0.05157137,0.00031197027],"about_ca_topic_score_codex":0.0002784106,"about_ca_topic_score_gemma":0.00079520984,"teacher_disagreement_score":0.03232874,"about_ca_system_score_codex":0.000060348044,"about_ca_system_score_gemma":0.00004829535,"threshold_uncertainty_score":0.99990743},"labels":[],"label_agreement":null},{"id":"W2041520574","doi":"10.1159/000022955","title":"Ascertainment and Anticipation in Family Studies","year":2000,"lang":"en","type":"article","venue":"Human Heredity","topic":"Prenatal Screening and Diagnostics","field":"Medicine","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 Laval","funders":"National Cancer Institute","keywords":"Anticipation (artificial intelligence); Genetics; Biology; Family studies; Evolutionary biology; Psychology; Computer science; Artificial intelligence","score_opus":0.08826232376475761,"score_gpt":0.3731676979251463,"score_spread":0.2849053741603887,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2041520574","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9927849,0.0010103297,0.000003037359,0.00015121284,0.000033562024,0.0001067619,0.0000025663194,0.000029209637,0.0058783744],"genre_scores_gemma":[0.99888414,0.00027854677,0.00011207212,0.00020148832,0.00011472508,0.000007855691,0.0000112986145,0.000004278011,0.00038558073],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9995532,0.000019172701,0.00010935641,0.0001129459,0.00010236215,0.00010294532],"domain_scores_gemma":[0.9997796,0.000054656088,0.000013347715,0.000088877314,0.000016263184,0.000047273807],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.000105832456,0.00005678084,0.00012855977,0.000025673136,0.000045284887,0.000005796869,0.00001739659,0.000031977874,0.000097781114],"category_scores_gemma":[0.0000818275,0.000048497546,0.0000130287135,0.000041698317,0.0000484812,0.000032148248,0.000014880132,0.00007650273,0.000017721712],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00018370278,0.00044092105,0.87795466,0.00019963192,0.00007255785,0.00024194442,0.0024251665,0.00004315921,0.00094211247,0.00055172853,0.01222862,0.10471581],"study_design_scores_gemma":[0.0008120521,0.00017164189,0.99663764,0.00012491818,0.000021395126,0.0000047126778,0.00020985372,0.00010420898,0.00013767624,0.0004104665,0.001309997,0.000055418466],"about_ca_topic_score_codex":0.00022248762,"about_ca_topic_score_gemma":0.000101987345,"teacher_disagreement_score":0.11868301,"about_ca_system_score_codex":0.000032946828,"about_ca_system_score_gemma":0.0000073252886,"threshold_uncertainty_score":0.19776726},"labels":[],"label_agreement":null},{"id":"W2043582093","doi":"10.1159/000073737","title":"Heterogeneity in IBD Allele Sharing among Covariate-Defined Subgroups: Issues and Findings for Affected Relatives","year":2003,"lang":"en","type":"article","venue":"Human Heredity","topic":"Genetic Associations and Epidemiology","field":"Biochemistry, Genetics and Molecular Biology","cited_by":6,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Toronto; Lunenfeld-Tanenbaum Research Institute; Mount Sinai Hospital","funders":"Division of Mathematical Sciences; Canadian Institutes of Health Research","keywords":"Covariate; Statistic; Identity by descent; Linkage (software); Test statistic; Locus (genetics); Allele; Statistics; Genetics; Mathematics; Biology; Statistical hypothesis testing; Haplotype; Gene","score_opus":0.03891493203046967,"score_gpt":0.3111233177445235,"score_spread":0.2722083857140538,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2043582093","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99807906,0.00040827517,0.0006820679,0.00004745349,0.00007443918,0.00028020857,0.00001885546,0.000013933126,0.00039572208],"genre_scores_gemma":[0.9975964,0.000055643373,0.0016175158,0.00003968591,0.00009411127,0.00006091824,0.00014840357,0.000017081858,0.00037025174],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99888635,0.00013963084,0.00024069031,0.00040563924,0.0000486056,0.0002790827],"domain_scores_gemma":[0.9995711,0.000041289986,0.00008486438,0.00019912135,0.000046220124,0.000057421417],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0006258299,0.00014298984,0.00022538814,0.000038088157,0.00015848913,0.000019407622,0.00009200465,0.00023225516,0.000025399338],"category_scores_gemma":[0.0005470505,0.00014675011,0.00006204675,0.000054350592,0.000080663136,0.000005549528,0.00006395725,0.00008225216,0.000001355742],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.000021752003,0.00006419613,0.9596819,0.000021684496,0.000047933532,9.564827e-7,0.00013126901,0.000059437072,0.037030444,0.0013117815,0.0016034064,0.000025232808],"study_design_scores_gemma":[0.00092114013,0.00024457523,0.98651195,0.000009291092,0.000014682466,0.0000024128701,0.00006752934,0.00013164469,0.0067948755,0.0029797321,0.0021279315,0.00019425311],"about_ca_topic_score_codex":0.00014836609,"about_ca_topic_score_gemma":0.0014216866,"teacher_disagreement_score":0.030235568,"about_ca_system_score_codex":0.000022508155,"about_ca_system_score_gemma":0.000014750774,"threshold_uncertainty_score":0.5984296},"labels":[],"label_agreement":null},{"id":"W2047963327","doi":"10.1159/000320367","title":"Increasing Genotype-Phenotype Model Determinism: Application to Bivariate Reading/Language Traits and Epistatic Interactions in Language-Impaired Families","year":2010,"lang":"en","type":"article","venue":"Human Heredity","topic":"Genetics and Neurodevelopmental Disorders","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 Toronto; Centre for Addiction and Mental Health","funders":"National Institute on Deafness and Other Communication Disorders; March of Dimes Foundation","keywords":"Epistasis; Genetic architecture; Quantitative trait locus; Biology; Genetics; Phenotype; Genetic linkage; Computational biology; Genetic model; Psychology; Gene","score_opus":0.012236324015165579,"score_gpt":0.2812808600181423,"score_spread":0.26904453600297673,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2047963327","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9975895,0.000039634077,0.0013332575,0.000042395088,0.00006177809,0.00022587607,0.000021934029,0.00001643419,0.000669142],"genre_scores_gemma":[0.9961135,0.000008244026,0.0033707556,0.0001933016,0.000041619907,0.000038506092,0.000074634314,0.000022227117,0.00013725423],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9992121,0.00003372375,0.0001748099,0.0003148167,0.0000712151,0.00019334804],"domain_scores_gemma":[0.99966615,0.000011635795,0.000046666024,0.00016500228,0.00002421552,0.00008630626],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00014069394,0.0001299474,0.00010748771,0.000074603646,0.000107260596,0.000030193743,0.00011170094,0.00006152691,0.000011481286],"category_scores_gemma":[0.000064894426,0.00014113181,0.00002360064,0.00007234336,0.000043851327,0.0000059301487,0.00010052044,0.00012838635,0.000006942598],"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":[0.0000281489,0.000047896916,0.0018728058,0.000017728951,0.0000058304736,0.0000023944954,0.0017981055,0.000095628384,0.99029106,0.000049086404,0.00005070331,0.005740638],"study_design_scores_gemma":[0.00095588574,0.0001714742,0.9044178,0.000023478748,0.000026380698,0.000035776055,0.0015205196,0.005407348,0.08567552,0.0006702408,0.0005226896,0.00057288085],"about_ca_topic_score_codex":0.000329008,"about_ca_topic_score_gemma":0.0051690172,"teacher_disagreement_score":0.9046155,"about_ca_system_score_codex":0.000010855006,"about_ca_system_score_gemma":0.000031269694,"threshold_uncertainty_score":0.5755188},"labels":[],"label_agreement":null},{"id":"W2052926134","doi":"10.1159/000081447","title":"A Note on Inference of Trait Associations with SNP Haplotypes and Other Attributes in Generalized Linear Models","year":2004,"lang":"en","type":"article","venue":"Human Heredity","topic":"Genetic Mapping and Diversity in Plants and Animals","field":"Biochemistry, Genetics and Molecular Biology","cited_by":44,"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; St. Paul's Hospital","funders":"","keywords":"Inference; Haplotype; Trait; SNP; Heredity; Biology; Genetics; Single-nucleotide polymorphism; Statistics; Mathematics; Genotype; Computer science; Artificial intelligence; Gene","score_opus":0.059602173941208925,"score_gpt":0.28925398707351635,"score_spread":0.22965181313230743,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2052926134","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99816406,0.00005126005,0.0006514944,0.00005916109,0.0000130884,0.00006195233,0.00018081532,0.000005331855,0.0008128548],"genre_scores_gemma":[0.99892926,0.000020372063,0.0007497327,0.00010700422,0.000052347994,0.0000021339094,0.00004389254,0.000004282076,0.000090943904],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.999578,0.000017948825,0.00009284379,0.00014226086,0.00007197325,0.000096975404],"domain_scores_gemma":[0.9997935,0.000008382475,0.00004921048,0.00008613561,0.000032957127,0.000029760598],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00007177561,0.00007184919,0.0001088338,0.000023399196,0.00005308353,0.000007771465,0.00005654356,0.000071531125,0.000011096893],"category_scores_gemma":[0.000019309207,0.000060543218,0.000021392216,0.000030492789,0.0000456657,0.0000022726613,0.000023692377,0.00004560289,8.2618385e-7],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0007176555,0.0018132852,0.29676488,0.00020265192,0.00033180165,0.00002649565,0.0035735068,0.08124888,0.5796889,0.032395884,0.0020612115,0.0011748717],"study_design_scores_gemma":[0.015846064,0.005255755,0.7296538,0.00050871586,0.00015244372,0.000016382905,0.00049853494,0.0017322995,0.21112378,0.023372874,0.010301195,0.0015381823],"about_ca_topic_score_codex":0.00035984733,"about_ca_topic_score_gemma":0.00056911923,"teacher_disagreement_score":0.4328889,"about_ca_system_score_codex":0.000006222714,"about_ca_system_score_gemma":0.000029108985,"threshold_uncertainty_score":0.24688807},"labels":[],"label_agreement":null},{"id":"W2055948550","doi":"10.1159/000353345","title":"An Analytical Comparison of the Principal Component Method and the Mixed Effects Model for Association Studies in the Presence of Cryptic Relatedness and Population Stratification","year":2013,"lang":"en","type":"article","venue":"Human Heredity","topic":"Genetic Associations and Epidemiology","field":"Biochemistry, Genetics and Molecular Biology","cited_by":23,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Queen's University","funders":"Natural Sciences and Engineering Research Council of Canada","keywords":"Population stratification; Principal component analysis; Population; Association (psychology); Genetic association; Econometrics; Biology; Component (thermodynamics); Population structure; Statistics; Evolutionary biology; Computer science; Mathematics; Genetics; Psychology; Genotype; Medicine","score_opus":0.082625839832943,"score_gpt":0.402744904752088,"score_spread":0.320119064919145,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2055948550","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99471885,0.00019394314,0.0041202293,0.00031864172,0.00004399002,0.000588777,0.0000043055597,0.000001323776,0.000009965879],"genre_scores_gemma":[0.9988067,0.000017714712,0.001003149,0.00002283157,0.00002859183,0.00007202538,0.000025180623,0.000002881924,0.00002089661],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99873835,0.0006836144,0.00027640007,0.00013096344,0.00008819044,0.000082506966],"domain_scores_gemma":[0.9988595,0.00055638276,0.0002741697,0.00018298725,0.000115225615,0.000011722125],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0013376152,0.000060156402,0.00018475682,0.000010966603,0.00011273651,0.000008030605,0.00009926988,0.0000948677,3.9157547e-7],"category_scores_gemma":[0.00086438376,0.000032465377,0.00003336594,0.000037921895,0.00012098913,0.0000050435738,0.000036451493,0.00006721993,4.6101146e-8],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00006539462,0.00022482935,0.937582,0.00015817278,0.00015487264,2.057175e-8,0.0042039487,0.016284514,0.029319612,0.010263154,0.00082669867,0.00091678626],"study_design_scores_gemma":[0.0003820718,0.00005830176,0.7132486,0.000007698479,0.000044383414,1.9263277e-7,0.0003853772,0.27912366,0.00048549174,0.006232551,0.000002293998,0.000029339719],"about_ca_topic_score_codex":0.00014120921,"about_ca_topic_score_gemma":0.0001850343,"teacher_disagreement_score":0.26283914,"about_ca_system_score_codex":0.00001571647,"about_ca_system_score_gemma":0.000009386018,"threshold_uncertainty_score":0.13238998},"labels":[],"label_agreement":null},{"id":"W2058900411","doi":"10.1159/000067666","title":"Enhanced Pedigree Error Detection","year":2002,"lang":"en","type":"article","venue":"Human Heredity","topic":"Genetic Associations and Epidemiology","field":"Biochemistry, Genetics and Molecular Biology","cited_by":146,"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 Institute of Diabetes and Digestive and Kidney Diseases; National Human Genome Research Institute; National Institutes of Health","keywords":"Pedigree chart; Linkage (software); Computer science; Type I and type II errors; Statistics; Range (aeronautics); Software; Data mining; Biology; Genetics; Mathematics","score_opus":0.041006955384239666,"score_gpt":0.28474891040558153,"score_spread":0.24374195502134188,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2058900411","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9846737,0.00016802989,0.0038713126,0.00008366073,0.00028846387,0.00008250741,0.0000062081504,0.0000216905,0.010804472],"genre_scores_gemma":[0.99401855,0.000036211284,0.00020093205,0.00014611534,0.0008397712,0.000019743415,0.000030443627,0.000010849579,0.0046973773],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9992772,0.00006746652,0.00015769652,0.00023658933,0.0000630648,0.00019799953],"domain_scores_gemma":[0.99957085,0.000008467806,0.00007530736,0.0002402602,0.000051540916,0.000053585707],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00013690056,0.000091896,0.00010420474,0.000018999488,0.00015916993,0.000007642374,0.00009658429,0.00015910229,0.00036539562],"category_scores_gemma":[0.00011288793,0.000092889764,0.0000691989,0.000040684503,0.00004462847,0.0000017068247,0.000043455402,0.00007692268,0.00009138322],"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":[0.000012003005,0.00014668918,0.012473254,0.0000126530085,0.000058751706,0.0000017071679,0.00012999318,0.000078071425,0.9173613,0.000055082262,0.057091348,0.012579154],"study_design_scores_gemma":[0.0020501735,0.0014633114,0.58267975,0.000012546187,0.000075673175,0.000033111104,0.00025489437,0.0013647475,0.23816137,0.001558579,0.17137054,0.0009752932],"about_ca_topic_score_codex":0.00002539308,"about_ca_topic_score_gemma":0.00032352822,"teacher_disagreement_score":0.67919993,"about_ca_system_score_codex":0.000015554773,"about_ca_system_score_gemma":0.000005082158,"threshold_uncertainty_score":0.40008256},"labels":[],"label_agreement":null},{"id":"W2061274432","doi":"10.1159/000365923","title":"Inferring Gene Network from Candidate SNP Association Studies Using a Bayesian Graphical Model: Application to a Breast Cancer Case-Control Study from Ontario","year":2014,"lang":"en","type":"article","venue":"Human Heredity","topic":"Genetic Associations and Epidemiology","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":true,"ca_institutions":"Public Health Ontario; University of Toronto; Lunenfeld-Tanenbaum Research Institute; The Scarborough Hospital","funders":"Natural Sciences and Engineering Research Council of Canada; National Institutes of Health; National Cancer Institute; Cancer Care Ontario","keywords":"Single-nucleotide polymorphism; Genetic association; SNP; Posterior probability; Genome-wide association study; Candidate gene; Computational biology; Breast cancer; Biology; Bayesian network; Markov chain Monte Carlo; Genetics; Bayesian probability; Bioinformatics; Computer science; Gene; Cancer; Artificial intelligence; Genotype","score_opus":0.02882455763125636,"score_gpt":0.31402524645811786,"score_spread":0.2852006888268615,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2061274432","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9379022,0.00011004208,0.06080549,0.00016996668,0.00020936424,0.00044204586,0.000321357,0.000020955855,0.000018540592],"genre_scores_gemma":[0.99558896,0.00000997239,0.0018663831,0.00047605459,0.0016717493,0.00016174618,0.00014937924,0.000024190269,0.000051584946],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99820113,0.00031744345,0.00040140154,0.00056132843,0.0001517173,0.00036699197],"domain_scores_gemma":[0.99893564,0.00009360628,0.00027282798,0.0003862071,0.00018600827,0.00012570989],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00065058144,0.00021143367,0.00039807777,0.00003151574,0.00038299683,0.000029107832,0.00013863923,0.00023156812,0.000028800274],"category_scores_gemma":[0.00012274912,0.00021418552,0.00009045296,0.00008343681,0.000023866472,0.0000062224617,0.00012435499,0.00017201209,0.000002784502],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":true,"about_ca_topic_consensus":true,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.000039507588,0.00008380487,0.92086494,0.0000018988349,0.0004720858,0.0000036214244,0.0005143386,0.06989801,0.0064771236,0.000006987131,0.0010903645,0.0005473484],"study_design_scores_gemma":[0.0010751932,0.000113751674,0.95617086,0.0000117030195,0.0002972841,0.000005901091,0.00013323556,0.040012766,0.00006685579,0.0015459249,0.000265384,0.00030113955],"about_ca_topic_score_codex":0.09907608,"about_ca_topic_score_gemma":0.50206214,"teacher_disagreement_score":0.40298605,"about_ca_system_score_codex":0.00039190118,"about_ca_system_score_gemma":0.000084434374,"threshold_uncertainty_score":0.90692323},"labels":[],"label_agreement":null},{"id":"W2063784711","doi":"10.1159/000362878","title":"Population-Genetic Influences on Genomic Estimates of the Inbreeding Coefficient: A Global Perspective","year":2014,"lang":"en","type":"article","venue":"Human Heredity","topic":"Forensic and Genetic Research","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":"University of Manitoba","funders":"National Human Genome Research Institute; National Institutes of Health; Burroughs Wellcome Fund","keywords":"Inbreeding; Consanguinity; Identity by descent; Biology; Population; Genetic variation; Genetic diversity; Genetic load; Evolutionary biology; Genetics; Kinship; Demography; Genotype; Haplotype; Gene; Sociology","score_opus":0.020143459534844293,"score_gpt":0.3162320871062592,"score_spread":0.2960886275714149,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2063784711","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9954576,0.00013695401,0.00015210484,0.000061777726,0.00013372558,0.00012954483,0.000014910934,0.0000056694103,0.003907709],"genre_scores_gemma":[0.9994286,0.0000043334876,0.00021446732,0.000054665274,0.00021557751,0.0000052589853,0.000010577977,0.000006576765,0.00005999599],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9992088,0.00005824032,0.00014324278,0.00023163848,0.00019520058,0.00016288886],"domain_scores_gemma":[0.999465,0.000015144601,0.00007265909,0.0003007358,0.00010462575,0.00004184815],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00014167695,0.000095341355,0.00010463803,0.000015035044,0.00015755909,0.000016349015,0.00024688354,0.00007031687,0.000020459234],"category_scores_gemma":[0.00017771996,0.0000690616,0.00006903738,0.000079851554,0.00023182531,0.0000012884333,0.00012907267,0.00006149237,0.000005814315],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.000087299486,0.00015145018,0.84845203,0.000045612844,0.00008096673,7.5741053e-7,0.00025164385,0.006902058,0.12242534,0.015742825,0.0028178955,0.003042104],"study_design_scores_gemma":[0.00023950834,0.000313809,0.9807921,0.000018303148,0.000010380654,0.0000035336504,0.00010732667,0.00041025938,0.0100986175,0.0077037415,0.0002106404,0.00009178719],"about_ca_topic_score_codex":0.00041867213,"about_ca_topic_score_gemma":0.00021876671,"teacher_disagreement_score":0.13234004,"about_ca_system_score_codex":0.000038309343,"about_ca_system_score_gemma":0.0000384711,"threshold_uncertainty_score":0.28162503},"labels":[],"label_agreement":null},{"id":"W2075527847","doi":"10.1159/000324177","title":"Coordinated Conditional Simulation with SLINK and SUP of Many Markers Linked or Associated to a Trait in Large Pedigrees","year":2011,"lang":"en","type":"article","venue":"Human Heredity","topic":"Genetic Associations and Epidemiology","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":"Ontario Institute for Cancer Research","funders":"National Institutes of Health; University of Pittsburgh","keywords":"Pedigree chart; Linkage (software); Trait; Genetics; Quantitative trait locus; Locus (genetics); Genetic linkage; Software; Computer science; Identity by descent; R package; Computational biology; Biology; Genotype; Gene; Haplotype; Programming language","score_opus":0.03868824507270785,"score_gpt":0.2917879819860413,"score_spread":0.25309973691333343,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2075527847","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9976669,0.000014772852,0.001380815,0.00003342237,0.00002233585,0.00019950295,0.0001439429,0.000007788939,0.000530498],"genre_scores_gemma":[0.99854654,0.0000036892725,0.0005118195,0.00009621833,0.000052269403,0.000017619299,0.0003979797,0.000010416023,0.0003634737],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99915546,0.00011421082,0.00024591247,0.00022167247,0.00007016271,0.00019260001],"domain_scores_gemma":[0.99954545,0.00004153772,0.00012283478,0.00011281898,0.00011723825,0.000060093615],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00036915782,0.00010248701,0.00019274274,0.00005183307,0.000060033584,0.0000038035182,0.000069188136,0.00017769207,0.00018345687],"category_scores_gemma":[0.00024288557,0.00008798604,0.000029283436,0.000090909714,0.000056856003,0.0000036137128,0.00004199538,0.00007341168,0.0000013255612],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0005023897,0.00032672883,0.99062973,0.000024177225,0.00013099695,0.000007133226,0.000501474,0.0010373695,0.0047078705,0.00020826393,0.0017432582,0.00018062352],"study_design_scores_gemma":[0.0011930205,0.0006599964,0.9959099,0.000014114859,0.000018150733,0.0000016931803,0.00016012492,0.0012213257,0.00017538143,0.00025309357,0.0002758988,0.00011726616],"about_ca_topic_score_codex":0.00012316908,"about_ca_topic_score_gemma":0.002096977,"teacher_disagreement_score":0.005280219,"about_ca_system_score_codex":0.000018249653,"about_ca_system_score_gemma":0.0000443462,"threshold_uncertainty_score":0.35879666},"labels":[],"label_agreement":null},{"id":"W2078119326","doi":"10.1159/000338943","title":"Efficient Adaptively Weighted Analysis of Secondary Phenotypes in Case-Control Genome-Wide Association Studies","year":2012,"lang":"en","type":"article","venue":"Human Heredity","topic":"Genetic Associations and Epidemiology","field":"Biochemistry, Genetics and Molecular Biology","cited_by":27,"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; York University; National Cancer Institute; NYU Langone Medical Center","keywords":"Population; Genetics; Single-nucleotide polymorphism; Biology; Genotype; Gene; Medicine","score_opus":0.02523457724282416,"score_gpt":0.2883427373985767,"score_spread":0.2631081601557525,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2078119326","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99636656,0.002312889,0.00047846217,0.00008508056,0.00012691176,0.00012898746,0.000112309404,0.0000061185515,0.00038270507],"genre_scores_gemma":[0.99902344,0.00003874375,0.00025838864,0.00015776373,0.00020402185,0.000019237783,0.00009135724,0.000008158562,0.00019891837],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9987101,0.00030439143,0.00038093815,0.00020505194,0.00010006122,0.0002994586],"domain_scores_gemma":[0.99901897,0.00026401965,0.0003143846,0.0001869591,0.00016375483,0.000051935764],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0011419905,0.00011924607,0.00040119336,0.00012775233,0.00008999551,0.0000033861304,0.00007418654,0.00017334035,0.00008036728],"category_scores_gemma":[0.0007147531,0.000113657086,0.00014934853,0.00022819356,0.00004562656,0.0000023548068,0.00005277362,0.0000994415,0.0000041390067],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.000017581082,0.00014739817,0.98968714,0.000010392596,0.0017527185,0.0000033586205,0.0004520704,0.0027386777,0.0039684135,0.00003043167,0.0010166491,0.00017516757],"study_design_scores_gemma":[0.00046408287,0.000070063536,0.99689645,0.0000022601846,0.00044013394,0.0000015921747,0.00044099125,0.000582759,0.0002970651,0.00004161614,0.0006455222,0.00011747645],"about_ca_topic_score_codex":0.00012032431,"about_ca_topic_score_gemma":0.0009786547,"teacher_disagreement_score":0.007209296,"about_ca_system_score_codex":0.00012228984,"about_ca_system_score_gemma":0.000029982762,"threshold_uncertainty_score":0.46348014},"labels":[],"label_agreement":null},{"id":"W2080742000","doi":"10.1159/000228921","title":"A New Strategy for Linkage Analysis under Epistasis Taking into Account Genetic Heterogeneity","year":2009,"lang":"en","type":"article","venue":"Human Heredity","topic":"Genetic Associations and Epidemiology","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":true,"ca_institutions":"Université Laval","funders":"Canadian Institutes of Health Research","keywords":"Epistasis; Locus (genetics); Genetics; Biology; Genetic linkage; Genetic heterogeneity; Locus heterogeneity; Pedigree chart; Quantitative trait locus; Gene; Computational biology; Evolutionary biology; Phenotype","score_opus":0.05154504885191007,"score_gpt":0.3509570198624404,"score_spread":0.2994119710105303,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2080742000","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.8655918,0.0005798333,0.13296352,0.00022676405,0.0000870506,0.00020180173,0.000029263776,0.000020053016,0.00029986474],"genre_scores_gemma":[0.9869909,0.000048552243,0.010881194,0.0005523334,0.0008071739,0.000019420602,0.00033303874,0.000015178725,0.00035216744],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99851984,0.00010355324,0.0003800169,0.00051372976,0.00010931564,0.00037354536],"domain_scores_gemma":[0.9989832,0.000026899666,0.0002574227,0.00047539076,0.000113850205,0.00014323258],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00031907053,0.00020448264,0.0003325411,0.00007732014,0.00026065,0.000043404572,0.00024070987,0.00028799297,0.00010193671],"category_scores_gemma":[0.00009927306,0.00020685882,0.00034262842,0.00017620418,0.00003905899,0.000003818352,0.00005127503,0.00009324569,0.0000066430407],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00022791863,0.0008112735,0.4310992,0.00010808641,0.005224113,0.000014256091,0.00041204126,0.071124084,0.30141073,0.0023635824,0.06591712,0.121287584],"study_design_scores_gemma":[0.00058036466,0.00049163116,0.9827595,0.0000036941997,0.00040548935,0.0000029376686,0.000055552748,0.0005638469,0.0036109344,0.007460623,0.00373565,0.00032982745],"about_ca_topic_score_codex":0.00032359138,"about_ca_topic_score_gemma":0.0019636573,"teacher_disagreement_score":0.55166024,"about_ca_system_score_codex":0.000053963944,"about_ca_system_score_gemma":0.000093640236,"threshold_uncertainty_score":0.8435458},"labels":[],"label_agreement":null},{"id":"W2093495067","doi":"10.1159/000143406","title":"Estimating Disease Risk Associated with Mutated Genes in Family-Based Designs","year":2008,"lang":"en","type":"article","venue":"Human Heredity","topic":"Genetic Associations and Epidemiology","field":"Biochemistry, Genetics and Molecular Biology","cited_by":18,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":true,"ca_institutions":"Alberta Cancer Foundation; Lunenfeld-Tanenbaum Research Institute; Mount Sinai Hospital","funders":"Institute of Genetics; Canadian Institutes of Health Research","keywords":"Pedigree chart; Penetrance; Proband; Genetics; Mutation; Population; Family history; Biology; Computer science; Statistics; Econometrics; Gene; Mathematics; Medicine; Internal medicine; Environmental health","score_opus":0.049529813479669574,"score_gpt":0.28190445695523797,"score_spread":0.2323746434755684,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2093495067","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9926346,0.00020043184,0.006638464,0.00003286313,0.00006993068,0.00016807244,0.000054661235,0.000027964088,0.00017299321],"genre_scores_gemma":[0.9956057,0.00001785675,0.0034278757,0.00013656268,0.00014657654,0.00003986956,0.00047239507,0.000021348045,0.00013180316],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99868035,0.00030581368,0.00025426064,0.00034462637,0.000110549954,0.00030438663],"domain_scores_gemma":[0.99929553,0.000054465185,0.00018769506,0.00025979333,0.00009029332,0.00011222272],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0003656462,0.00015759355,0.0002001681,0.00004383345,0.00026629402,0.000007296711,0.00012114493,0.00013920206,0.00002038528],"category_scores_gemma":[0.000516302,0.00014442798,0.00006209608,0.000095300726,0.00012673563,0.0000026294435,0.000032884458,0.00012700155,0.0000056615863],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.000041595104,0.00015309842,0.96689415,0.0000054899438,0.000039231894,0.00003155026,0.00003799701,0.025045143,0.006247186,0.0000025134805,0.0013131559,0.00018891665],"study_design_scores_gemma":[0.00095785974,0.0001813671,0.9866647,0.00001677343,0.000026517399,0.0000017802829,0.000016617436,0.0111114215,0.0005572902,0.00011973153,0.00014654658,0.00019939996],"about_ca_topic_score_codex":0.0002570683,"about_ca_topic_score_gemma":0.00053012127,"teacher_disagreement_score":0.019770574,"about_ca_system_score_codex":0.00004296006,"about_ca_system_score_gemma":0.00015745856,"threshold_uncertainty_score":0.58896023},"labels":[],"label_agreement":null},{"id":"W2094317540","doi":"10.1159/000099829","title":"Imputation of Missing Ages in Pedigree Data","year":2007,"lang":"en","type":"article","venue":"Human Heredity","topic":"Statistical Methods and Bayesian Inference","field":"Mathematics","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; Ontario Institute for Cancer Research","funders":"","keywords":"Imputation (statistics); Missing data; Statistics; Regression; Pedigree chart; Regression analysis; Linear regression; Mathematics; Medicine; Computer science; Biology; Genetics","score_opus":0.2951842863507974,"score_gpt":0.4897296952113052,"score_spread":0.1945454088605078,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2094317540","genre_codex":"methods","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"methods","genre_consensus":null,"domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.17524956,0.000025036326,0.81975865,0.000023706609,0.00009695584,0.000086107604,0.000037432354,0.000023609837,0.004698916],"genre_scores_gemma":[0.5447706,7.795795e-7,0.4550627,0.000008418417,0.0001198227,4.998883e-7,0.000014982051,0.000006234673,0.000015964799],"study_design_codex":"theoretical_or_conceptual","study_design_gemma":"theoretical_or_conceptual","domain_scores_codex":[0.9991406,0.00006400887,0.00033120686,0.00016176318,0.00015659803,0.00014580185],"domain_scores_gemma":[0.99842215,0.0010316792,0.00011330298,0.00035122363,0.000040596344,0.000041068783],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0013500222,0.00006680705,0.00017193936,0.000052960997,0.000036477424,0.00001225399,0.00020002773,0.0000526302,0.00016799395],"category_scores_gemma":[0.0015407386,0.0000612881,0.000014757711,0.00009460012,0.00006044105,0.00008650826,0.00008268074,0.0001104396,0.000002539766],"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":[0.000028272514,0.0003166429,0.018939698,0.00049823866,0.0000138767555,0.00009787515,0.0010696346,2.028346e-7,0.002567631,0.5156946,0.00368094,0.45709234],"study_design_scores_gemma":[0.0001823623,0.00002954036,0.11703387,0.00006724885,0.00001042955,0.000003045277,0.000067193425,0.00032731364,0.0006048027,0.88153744,0.00006507801,0.00007167369],"about_ca_topic_score_codex":0.000113883514,"about_ca_topic_score_gemma":0.00033329654,"teacher_disagreement_score":0.45702067,"about_ca_system_score_codex":0.000022316755,"about_ca_system_score_gemma":0.000016643207,"threshold_uncertainty_score":0.24992561},"labels":[],"label_agreement":null},{"id":"W2094624574","doi":"10.1159/000053354","title":"Mutation Analysis of a Mauritian Hereditary Breast Cancer Family Reveals the <i>BRCA2</i> 6503delTT Mutation Previously Found to Recur in Different Ethnic Populations","year":2001,"lang":"en","type":"article","venue":"Human Heredity","topic":"BRCA gene mutations in cancer","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":"McGill University; Hotel Dieu Hospital; Montreal General Hospital","funders":"National Cancer Institute; Mauritius Research Council","keywords":"Haplotype; Mutation; Genetics; Population; Founder effect; Ethnic group; Breast cancer; Biology; Incidence (geometry); Cancer; Demography; Allele; Gene","score_opus":0.043824073671317465,"score_gpt":0.3325247121818634,"score_spread":0.28870063851054595,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2094624574","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9941071,0.0019735151,0.0012350375,0.0007051319,0.00041294275,0.0007658495,0.00034977743,0.000024862808,0.0004257435],"genre_scores_gemma":[0.9966534,0.00020386712,0.0002986996,0.00030562514,0.00071775634,0.00038841128,0.0010276175,0.00004033608,0.00036427914],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.99756324,0.00030809984,0.0007199588,0.0006253956,0.0003986533,0.00038462706],"domain_scores_gemma":[0.9984606,0.000047686208,0.0003008292,0.00074168027,0.00032809968,0.000121142984],"candidate_categories":["metaepi_narrow"],"consensus_categories":[],"category_scores_codex":[0.00045693832,0.00028973017,0.00040293112,0.0003194236,0.0002170969,0.000036987338,0.00035298718,0.00022515161,0.00022795348],"category_scores_gemma":[0.0000886351,0.00025740813,0.0002190253,0.0011399416,0.0001331549,0.000023692344,0.00010962533,0.00016766333,0.000006163534],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":true,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0007979086,0.0015285262,0.111194156,0.00030095698,0.0033518698,0.00011854925,0.007905386,0.12802863,0.6543916,0.001529021,0.047404543,0.04344889],"study_design_scores_gemma":[0.00066051714,0.00016557089,0.99355966,0.00007185816,0.0005801769,0.00002906505,0.00023763592,0.0011825012,0.00083913916,0.0008958167,0.0014480506,0.0003299836],"about_ca_topic_score_codex":0.0006855416,"about_ca_topic_score_gemma":0.051733453,"teacher_disagreement_score":0.8823655,"about_ca_system_score_codex":0.00037226238,"about_ca_system_score_gemma":0.0001489625,"threshold_uncertainty_score":0.99998784},"labels":[],"label_agreement":null},{"id":"W2116037283","doi":"10.1159/000339906","title":"Natural and Orthogonal Interaction Framework for Modeling Gene-Environment Interactions with Application to Lung Cancer","year":2012,"lang":"en","type":"article","venue":"Human Heredity","topic":"Genetic Associations and Epidemiology","field":"Biochemistry, Genetics and Molecular Biology","cited_by":16,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Toronto","funders":"National Institute of Arthritis and Musculoskeletal and Skin Diseases; National Cancer Institute; National Heart, Lung, and Blood Institute; National Center for Research Resources; National Institute of General Medical Sciences; U.S. Public Health Service","keywords":"Statistical power; Gene–environment interaction; Statistical model; Gene interaction; Genetic model; Computer science; Biology; Statistics; Mathematics; Genetics; Genotype; Gene","score_opus":0.022956831135116103,"score_gpt":0.33396998070615763,"score_spread":0.31101314957104154,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2116037283","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.66439235,0.0002459208,0.334831,0.00015701262,0.00014663958,0.00018611099,0.00001428712,0.000004709379,0.000021986305],"genre_scores_gemma":[0.98317736,0.0000366207,0.015140883,0.00019740559,0.0008965237,0.00031058802,0.00013672009,0.000011811631,0.00009208438],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9994445,0.000025230296,0.00012131822,0.0001930518,0.000043842316,0.00017206972],"domain_scores_gemma":[0.9996853,0.000018911556,0.000063356325,0.00012689941,0.00003514322,0.00007038909],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00012145741,0.000084673375,0.0000843178,0.000018610275,0.00015343775,0.000008587242,0.000041351548,0.00007133351,0.000011578278],"category_scores_gemma":[0.000027682328,0.00007652164,0.000028890045,0.000019517227,0.00001581024,0.0000068765835,0.000040061073,0.00008665476,0.0000014407688],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00035903527,0.0003338037,0.67333657,0.00007229033,0.0004313479,1.9104327e-7,0.00083612755,0.05298283,0.25019056,0.002332332,0.005891532,0.013233398],"study_design_scores_gemma":[0.0016801402,0.0007313511,0.7421786,0.000108818655,0.00041759328,0.000053245643,0.0010781164,0.17613655,0.01387266,0.00256253,0.059731357,0.0014489989],"about_ca_topic_score_codex":0.0000407683,"about_ca_topic_score_gemma":0.00014535514,"teacher_disagreement_score":0.31969014,"about_ca_system_score_codex":0.000045763576,"about_ca_system_score_gemma":0.000010086998,"threshold_uncertainty_score":0.3120462},"labels":[],"label_agreement":null},{"id":"W2141685742","doi":"10.1159/000371579","title":"Prioritizing Rare Variants with Conditional Likelihood Ratios","year":2015,"lang":"en","type":"article","venue":"Human Heredity","topic":"Genomics and Rare Diseases","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":"Public Health Ontario; University of Toronto","funders":"Ontario Ministry of Research and Innovation; Natural Sciences and Engineering Research Council of Canada; European Commission; Epilepsy Research UK; Canadian Institutes of Health Research; National Institute for Health and Care Research; Cancer Research UK; Wellcome Trust; South London and Maudsley NHS Foundation Trust","keywords":"Ranking (information retrieval); Statistics; Statistical hypothesis testing; p-value; Multiple comparisons problem; False discovery rate; Sequence (biology); Set (abstract data type); Computer science; Mathematics; Biology; Genetics; Artificial intelligence; Gene","score_opus":0.02400139833496208,"score_gpt":0.2586968578512845,"score_spread":0.23469545951632242,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2141685742","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99620634,0.00023404327,0.00048823844,0.00005600338,0.00012584176,0.00012378347,0.0001226233,0.000016165197,0.0026269518],"genre_scores_gemma":[0.99745554,0.000004836261,0.0003243992,0.00019791212,0.0007818151,0.000014218597,0.00091593945,0.000015297446,0.00029003996],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9993535,0.000028671566,0.000102320795,0.00022704365,0.00012504573,0.00016340679],"domain_scores_gemma":[0.9994552,0.0000031014824,0.000045938963,0.00019809161,0.00013573267,0.00016192964],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.000080843616,0.00010332451,0.00008490567,0.000015910815,0.00011541426,0.000035530353,0.000101900965,0.0000676071,0.000033985765],"category_scores_gemma":[0.000025582065,0.00009105068,0.00003695342,0.000027578953,0.00005294713,0.0000046474834,0.00005342811,0.000052380838,0.000020089577],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00086400827,0.0014992277,0.10223919,0.00016609761,0.0006636132,0.000823946,0.000724141,0.00022945178,0.6211591,0.009743794,0.25992748,0.0019599556],"study_design_scores_gemma":[0.01552024,0.0045608305,0.6301041,0.00015140716,0.00029842072,0.0010311595,0.0024588688,0.00017788964,0.055647247,0.03266457,0.25451356,0.0028716791],"about_ca_topic_score_codex":0.000015154741,"about_ca_topic_score_gemma":0.00006810701,"teacher_disagreement_score":0.5655118,"about_ca_system_score_codex":0.000014389755,"about_ca_system_score_gemma":0.00017493874,"threshold_uncertainty_score":0.3712939},"labels":[],"label_agreement":null},{"id":"W2506162896","doi":"10.1159/000446475","title":"When Is an Endophenotype Useful to Detect Association to a Disease? Exploring the Relationships between Disease Status, Endophenotype and Genetic Polymorphisms","year":2016,"lang":"en","type":"article","venue":"Human Heredity","topic":"Genetic Associations and Epidemiology","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":"Institut Universitaire en Santé Mentale de Québec; Université Laval","funders":"Canadian Institutes of Health Research","keywords":"Endophenotype; Locus (genetics); Allele; Disease; Genetics; Biology; Medicine; Internal medicine; Neuroscience; Cognition; Gene","score_opus":0.0766884189978016,"score_gpt":0.27786481553531395,"score_spread":0.20117639653751235,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2506162896","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9931577,0.00024413156,0.0025932917,0.0029977662,0.00018745783,0.00043867863,0.00030929578,0.00002900363,0.000042663632],"genre_scores_gemma":[0.99618286,0.000056257428,0.0012608501,0.000542776,0.0010138438,0.00018065856,0.00007099809,0.000033970788,0.0006577628],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99798775,0.00045194145,0.0003152723,0.0005519477,0.00021098558,0.0004821062],"domain_scores_gemma":[0.9982763,0.00017602088,0.00013746378,0.00060300535,0.00011964892,0.00068754534],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0004717495,0.00020344635,0.00019585826,0.000057704223,0.0004738355,0.00004483874,0.0002273945,0.00010679481,0.00007572134],"category_scores_gemma":[0.0013888574,0.00014994538,0.00007352546,0.00009179687,0.000045178087,0.000015254847,0.00019652634,0.00011614015,0.00006296754],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00006516836,0.000022375363,0.9815752,0.0000056891736,0.00006247043,0.0000024999601,0.00039597307,0.000023925582,0.008489544,0.000038950006,0.0041563297,0.005161902],"study_design_scores_gemma":[0.00029869657,0.00017954787,0.98147464,0.000012392773,0.00007924755,5.541907e-7,0.000032942688,0.0000040691457,0.00053201703,0.006002738,0.011158648,0.00022450591],"about_ca_topic_score_codex":0.00011778715,"about_ca_topic_score_gemma":0.00028203797,"teacher_disagreement_score":0.0079575265,"about_ca_system_score_codex":0.000121371064,"about_ca_system_score_gemma":0.00009008636,"threshold_uncertainty_score":0.61145955},"labels":[],"label_agreement":null},{"id":"W2752644694","doi":"10.1159/000479428","title":"Variance Formulae for Correlation Measures of Linkage Disequilibrium","year":2016,"lang":"en","type":"article","venue":"Human Heredity","topic":"Genetic Associations and Epidemiology","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; Dalhousie University","funders":"","keywords":"Linkage disequilibrium; Disequilibrium; Linkage (software); Correlation; Variance (accounting); Mathematics; Statistics; Genetics; Biology; Allele; Haplotype; Medicine","score_opus":0.04154434058621321,"score_gpt":0.292317439945841,"score_spread":0.25077309935962777,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2752644694","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.86858404,0.00015435882,0.129713,0.00019587197,0.00025074786,0.00020066656,0.00009334764,0.000009520076,0.00079843716],"genre_scores_gemma":[0.9967977,0.000025072772,0.0011337444,0.000040737883,0.0004062011,0.000028195984,0.00007590007,0.0000101431315,0.0014823136],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9993392,0.000050023686,0.0002164762,0.00018401317,0.00005723655,0.00015300918],"domain_scores_gemma":[0.99942833,0.00004857341,0.0001450725,0.00022055331,0.00012162664,0.000035814013],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0003082395,0.00007510266,0.00013047691,0.000014659393,0.00006323172,0.000002769533,0.000098803954,0.00014282942,0.000025963347],"category_scores_gemma":[0.0003715008,0.00005603346,0.00008752234,0.0000218001,0.00005689776,0.000003049668,0.000036627374,0.000023318273,0.0000037653451],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.000065549655,0.00007739444,0.15266015,0.000031657502,0.00007098774,1.7975415e-7,0.000036580906,0.000057811878,0.8198204,0.0021162992,0.020221882,0.0048410785],"study_design_scores_gemma":[0.0021102005,0.0007686161,0.8731159,0.00004104272,0.000059764858,0.0000029487874,0.000020743006,0.00025779923,0.049097158,0.0143286325,0.059861835,0.00033536955],"about_ca_topic_score_codex":0.0000092068285,"about_ca_topic_score_gemma":0.00003785341,"teacher_disagreement_score":0.7707233,"about_ca_system_score_codex":0.000012494838,"about_ca_system_score_gemma":0.000029996148,"threshold_uncertainty_score":0.22849782},"labels":[],"label_agreement":null},{"id":"W2938734262","doi":"10.1159/000501334","title":"The Contribution Plot: Decomposition and Graphical Display of the RV Coefficient, with Application to Genetic and Brain Imaging Biomarkers of Alzheimer’s Disease","year":2019,"lang":"en","type":"preprint","venue":"Human Heredity","topic":"Dementia and Cognitive Impairment Research","field":"Medicine","cited_by":1,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Simon Fraser University","funders":"National Institute on Aging","keywords":"Neuroimaging; Plot (graphics); Disease; Multivariate statistics; Alzheimer's Disease Neuroimaging Initiative; Neuroscience; Alzheimer's disease; Psychology; Computer science; Artificial intelligence; Medicine; Statistics; Mathematics; Internal medicine; Machine learning","score_opus":0.011838712689904558,"score_gpt":0.3216233020448571,"score_spread":0.30978458935495257,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2938734262","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99050814,0.0008821838,0.0045819497,0.0015962038,0.000052107996,0.0022305958,0.00008193585,0.000010473777,0.000056382196],"genre_scores_gemma":[0.99958014,0.00004390667,0.000027322045,0.00007447285,0.000044047338,0.00010636767,0.00010223963,0.000011459344,0.000010056582],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99873537,0.00015178128,0.00023826033,0.0003110777,0.0003975787,0.00016593134],"domain_scores_gemma":[0.9989629,0.00011362174,0.00017373958,0.00036236306,0.0002537099,0.00013367123],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00042950833,0.00013485034,0.00020939867,0.00006940696,0.00017237922,0.000031880376,0.000103415245,0.000048732207,0.0000054672055],"category_scores_gemma":[0.000058287165,0.00007892617,0.000061926665,0.00010543307,0.00045219722,0.000019643041,0.00028534696,0.00019125728,6.324542e-7],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00082040316,0.0002457883,0.9817814,0.00031742567,0.00025906318,0.0000032855826,0.00010061502,0.00002271464,0.010997739,0.0004683627,0.0003817512,0.004601402],"study_design_scores_gemma":[0.00097797,0.00016173476,0.99351317,0.00034292534,0.00041874874,0.0000057271905,0.000047411668,0.0023297628,0.0016086099,0.0004128734,0.000099937046,0.00008112311],"about_ca_topic_score_codex":0.00007864494,"about_ca_topic_score_gemma":0.000037519563,"teacher_disagreement_score":0.011731726,"about_ca_system_score_codex":0.000026761585,"about_ca_system_score_gemma":0.00008646682,"threshold_uncertainty_score":0.32185158},"labels":[],"label_agreement":null},{"id":"W2953165036","doi":"10.1159/000486854","title":"Using Gene Genealogies to Localize Rare Variants Associated with Complex Traits in Diploid Populations","year":2018,"lang":"en","type":"article","venue":"Human Heredity","topic":"Genetic Associations and Epidemiology","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; Simon Fraser University","keywords":"Biology; Genetics; Ploidy; Gene; Phenotype; Evolutionary biology; Allele","score_opus":0.15256527467477915,"score_gpt":0.3568340775694893,"score_spread":0.20426880289471017,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2953165036","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.98950016,0.00003397089,0.009408037,0.00009523393,0.000100863275,0.0002084494,0.00008942729,0.000020719282,0.0005431073],"genre_scores_gemma":[0.99065244,0.0000026451032,0.008100445,0.00035043515,0.0003855049,0.00001580725,0.00034092038,0.000021332447,0.00013045844],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.998729,0.00017837198,0.00028137423,0.00035857235,0.000102687074,0.0003499955],"domain_scores_gemma":[0.9993928,0.000016207918,0.000115444476,0.00023081899,0.00015648479,0.00008822596],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0002760574,0.0001532571,0.00022993938,0.000057945308,0.00024161299,0.000017175327,0.0001599938,0.0001879574,0.00008091539],"category_scores_gemma":[0.0002695961,0.0001455905,0.000042979165,0.00017871712,0.000109605084,0.000003876019,0.000096825635,0.00007597564,0.000009234652],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00007570954,0.00030079484,0.46197748,0.000009568966,0.00014570483,0.000011394516,0.00044236885,0.004037817,0.5248811,0.00024609076,0.0072921007,0.0005798604],"study_design_scores_gemma":[0.00051218836,0.00029933194,0.99589753,0.000013223823,0.00001814557,0.000005800295,0.000053515352,0.0005098044,0.001151161,0.00053329114,0.0008055109,0.0002005004],"about_ca_topic_score_codex":0.0002772906,"about_ca_topic_score_gemma":0.0061358446,"teacher_disagreement_score":0.53392005,"about_ca_system_score_codex":0.00006869844,"about_ca_system_score_gemma":0.000062360516,"threshold_uncertainty_score":0.5937008},"labels":[],"label_agreement":null},{"id":"W4242935983","doi":"10.1159/000073726","title":"Preface","year":2003,"lang":"en","type":"article","venue":"Human Heredity","topic":"Genetic Associations and Epidemiology","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":"Computational biology; Biology; Evolutionary biology","score_opus":0.026072418645812733,"score_gpt":0.2899939166537065,"score_spread":0.2639214980078938,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4242935983","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.96747565,0.0001933822,0.0008695711,0.000040820054,0.00017145746,0.00006422011,0.000006056184,0.000010570249,0.03116827],"genre_scores_gemma":[0.99440885,0.00001818278,0.0008878139,0.0001731713,0.00019331161,0.000010144221,0.000041682448,0.000008197497,0.0042586727],"study_design_codex":"observational","study_design_gemma":"not_applicable","domain_scores_codex":[0.9993911,0.000103690356,0.00011422558,0.00018206864,0.000043783853,0.00016517806],"domain_scores_gemma":[0.99964106,0.000007030715,0.000044824275,0.00022208823,0.00003766416,0.00004730398],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00023497954,0.000069452864,0.0000810322,0.000009481887,0.0001048976,0.000005737534,0.000073590345,0.00010905169,0.00018771927],"category_scores_gemma":[0.00018536304,0.00006771354,0.000041274467,0.000029955556,0.000036592624,7.249016e-7,0.000024168054,0.00005067858,0.000037280264],"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":[0.000010121117,0.00019484061,0.48720777,0.000015158403,0.00009987689,0.0000027379401,0.00007188481,0.00017284373,0.21489413,0.0075441794,0.28883556,0.0009508918],"study_design_scores_gemma":[0.00051312393,0.0002197792,0.3259963,0.0000026880632,0.000014531656,0.000012416773,0.00007206523,0.000009090479,0.018656258,0.0032112177,0.65104187,0.00025065985],"about_ca_topic_score_codex":0.000011897535,"about_ca_topic_score_gemma":0.0000467122,"teacher_disagreement_score":0.3622063,"about_ca_system_score_codex":0.000008413296,"about_ca_system_score_gemma":0.000028547116,"threshold_uncertainty_score":0.27612782},"labels":[],"label_agreement":null},{"id":"W4283724494","doi":"10.1159/000525650","title":"Penalized Logistic Regression Analysis for Genetic Association Studies of Binary Phenotypes","year":2022,"lang":"en","type":"article","venue":"Human Heredity","topic":"Genetic Associations and Epidemiology","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":"Canada's Michael Smith Genome Sciences Centre; Simon Fraser University","funders":"","keywords":"Statistics; Mathematics; Logistic regression; Estimator; Binary data; Lasso (programming language); Binary number; Computer science","score_opus":0.08477605073196456,"score_gpt":0.3673931626076244,"score_spread":0.28261711187565985,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4283724494","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9964356,0.0017719119,0.001022541,0.00014985053,0.00020710421,0.00019073808,0.00012660645,0.000008556058,0.00008709307],"genre_scores_gemma":[0.9957644,0.00010239096,0.0018179631,0.000095503456,0.00019231705,0.00012358051,0.0004222392,0.000009956462,0.0014716788],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99877375,0.00030090267,0.0003272752,0.0002666159,0.00014592837,0.00018550483],"domain_scores_gemma":[0.99896884,0.0001576103,0.00041747742,0.00023657769,0.00019132119,0.000028164483],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00073054474,0.00010246342,0.00032964026,0.0000730487,0.00034555767,0.0000036930512,0.00014379593,0.00008357727,0.000115873736],"category_scores_gemma":[0.0008429487,0.00009626401,0.00021854066,0.00016904263,0.000046595913,0.0000012383753,0.0001658009,0.00006645999,9.311397e-7],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00014279272,0.000263292,0.80185276,0.000069743124,0.0027866897,0.0000015020768,0.00027389644,0.016100671,0.11176191,0.0001226272,0.06622954,0.00039458292],"study_design_scores_gemma":[0.0011687047,0.0010543431,0.97713476,0.000005555704,0.00107452,0.000001355032,0.0007715382,0.0008363508,0.001998697,0.0027969482,0.012877637,0.00027961438],"about_ca_topic_score_codex":0.000042622283,"about_ca_topic_score_gemma":0.00007729835,"teacher_disagreement_score":0.17528199,"about_ca_system_score_codex":0.000091963695,"about_ca_system_score_gemma":0.000038635346,"threshold_uncertainty_score":0.39255324},"labels":[],"label_agreement":null},{"id":"W4285800430","doi":"10.1159/000525663","title":"Mutational Screening for Mitochondrial tRNA Genes in 100 Women with Pre-Eclampsia","year":2022,"lang":"en","type":"article","venue":"Human Heredity","topic":"Mitochondrial Function and Pathology","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":"Leukemia and Lymphoma Society of Canada","keywords":"Transfer RNA; Genetics; Mitochondrial DNA; Biology; Gene; Haplogroup; Mutation; Allele; RNA; Haplotype","score_opus":0.026678886225845543,"score_gpt":0.2801664170368922,"score_spread":0.2534875308110467,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4285800430","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9899852,0.00008974814,0.008182407,0.00006101396,0.0006737488,0.00042722336,0.00009894248,0.0000164201,0.0004652718],"genre_scores_gemma":[0.9883447,0.000003483426,0.0043625087,0.00033648143,0.0019937896,0.0010223626,0.0007924219,0.000032006603,0.003112234],"study_design_codex":"bench_or_experimental","study_design_gemma":"not_applicable","domain_scores_codex":[0.9989733,0.00011308601,0.00017883517,0.00034971992,0.00014225501,0.00024278744],"domain_scores_gemma":[0.9996185,0.000019277228,0.0000745273,0.00018740851,0.000042090673,0.000058227844],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00016274756,0.00011689109,0.00013316123,0.000055437587,0.00027454473,0.000015142718,0.0001386993,0.00007519593,0.0006411288],"category_scores_gemma":[0.000029288422,0.000118646945,0.000046715813,0.0000757451,0.000050910734,0.0000040071104,0.00007980137,0.00012442762,0.0000018980314],"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":[0.007973706,0.00043303418,0.013948213,0.0000555192,0.00013335033,0.00004463744,0.0013900715,0.0077489265,0.93472576,0.00104077,0.028130641,0.0043753576],"study_design_scores_gemma":[0.016689094,0.008729898,0.06483499,0.000017930715,0.000050150313,0.00028268504,0.0021159193,0.00050719734,0.02821618,0.0021648225,0.875172,0.0012191164],"about_ca_topic_score_codex":0.000027807282,"about_ca_topic_score_gemma":0.00020351411,"teacher_disagreement_score":0.9065096,"about_ca_system_score_codex":0.000038207636,"about_ca_system_score_gemma":0.00007851255,"threshold_uncertainty_score":0.7019911},"labels":[],"label_agreement":null},{"id":"W4292331552","doi":"10.1159/000488519","title":"46th European Mathematical Genetics Meeting (EMGM) 2018, Cagliari, Italy, April 18-20, 2018: Abstracts","year":2018,"lang":"en","type":"article","venue":"Human Heredity","topic":"Regional Development and Environment","field":"Social Sciences","cited_by":17,"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":"Barts and The London School of Medicine and Dentistry; Medical Research Council; Stanley Center for Psychiatric Research, Broad Institute; Universität Basel; Deutsches Zentrum für Lungenforschung; Institute of Genetics; Tartu Ülikool; Massachusetts General Hospital; Università degli Studi di Brescia; Deutsches Zentrum für Herz-Kreislaufforschung; Centre Hospitalier Universitaire Vaudois; Universität zu Lübeck; Karolinska Institutet; Lunds Universitet; Sun Yat-sen University; King Abdulaziz University; Universität Heidelberg; University of Leicester; Université de Lille; Broad Institute; Sahlgrenska Universitetssjukhuset; Wellcome Trust; National Institute for Health and Care Research; Queen Mary University of London; Technische Universität München; Helsingin Yliopisto; U.S. Department of Veterans Affairs","keywords":"Genetics; Evolutionary biology; Biology","score_opus":0.08618641216971311,"score_gpt":0.3076906120364332,"score_spread":0.2215041998667201,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4292331552","genre_codex":"other","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":null,"domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.47497195,0.000056515135,0.00006604299,0.00041441462,0.00056031893,0.00015291988,0.0000049356872,0.00008304846,0.52368987],"genre_scores_gemma":[0.9776291,0.00006959845,0.0014744322,0.00016976913,0.0030183864,0.0000049546916,0.000018721918,0.00003142272,0.017583571],"study_design_codex":"not_applicable","study_design_gemma":"not_applicable","domain_scores_codex":[0.997819,0.00019741103,0.00038974045,0.0003555987,0.000730486,0.00050774746],"domain_scores_gemma":[0.99915236,0.000080118145,0.00015758746,0.0003005192,0.000049555394,0.00025984368],"candidate_categories":["insufficient_payload"],"consensus_categories":["insufficient_payload"],"category_scores_codex":[0.0014594803,0.00018505649,0.00019371195,0.000041952266,0.0010436687,0.00013649289,0.0004348219,0.000110233224,0.0027352667],"category_scores_gemma":[0.0001159396,0.00017574237,0.00008740769,0.00009275189,0.0007876618,0.00014707362,0.00017938075,0.00017531887,0.0046141814],"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":[0.000027525595,0.00067902246,0.0243373,0.00010427116,0.00016174513,0.00012904125,0.028505698,0.000051597388,0.0033412091,0.010325762,0.9258696,0.0064672437],"study_design_scores_gemma":[0.00037631067,0.000111072135,0.21563728,0.00008903631,0.000051172643,0.000004152377,0.0012343138,0.000029456209,0.00042080664,0.011549314,0.76993567,0.00056140864],"about_ca_topic_score_codex":0.00019216015,"about_ca_topic_score_gemma":0.00068278617,"teacher_disagreement_score":0.50610626,"about_ca_system_score_codex":0.00017000719,"about_ca_system_score_gemma":0.000065994216,"threshold_uncertainty_score":0.9981764},"labels":[],"label_agreement":null},{"id":"W4367058914","doi":"10.1159/000529559","title":"Methods and Software to Analyze Gene-Environment Interactions under a Case-Mother-Control-Mother Design with Partially Missing Child Genotype","year":2023,"lang":"en","type":"article","venue":"Human Heredity","topic":"Health, Environment, Cognitive Aging","field":"Environmental Science","cited_by":1,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Centre hospitalier universitaire de Québec; Institut National de Santé Publique du Québec; Université Laval","funders":"National Institute of Environmental Health Sciences","keywords":"Covariate; Logistic regression; Restricted maximum likelihood; Genotype; Statistics; Medicine; Biology; Maximum likelihood; Mathematics; Genetics; Gene","score_opus":0.04969795592361259,"score_gpt":0.3399055477831,"score_spread":0.2902075918594874,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4367058914","genre_codex":"methods","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":null,"domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.4369028,0.000037506812,0.560461,0.0008461465,0.00006765218,0.0007480033,0.000020365205,0.00015123765,0.000765279],"genre_scores_gemma":[0.91475827,0.00002151196,0.08256346,0.0017002366,0.00017305928,0.000114657145,0.000009133768,0.00009377428,0.00056588964],"study_design_codex":"design_other","study_design_gemma":"observational","domain_scores_codex":[0.9972251,0.0006478719,0.0003174555,0.0008781503,0.0003351019,0.00059628626],"domain_scores_gemma":[0.99864775,0.00029935164,0.00012807257,0.0005207694,0.0000057239777,0.00039834253],"candidate_categories":["metaepi_narrow","insufficient_payload"],"consensus_categories":[],"category_scores_codex":[0.001287616,0.0003034085,0.00028469219,0.000095189105,0.0008353104,0.00007890677,0.00016173882,0.00008461077,0.0033433086],"category_scores_gemma":[0.00006638391,0.00027726774,0.00005534727,0.0002614495,0.00024563292,0.00024078564,0.00018490228,0.00031331633,0.0007511518],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0005432867,0.0010593723,0.17324063,0.00012341393,0.0007959945,0.0030299993,0.0112507045,0.28263128,0.1326994,0.00008022307,0.006261794,0.3882839],"study_design_scores_gemma":[0.0024547745,0.0007528251,0.9417081,0.00013702249,0.00035646206,0.0009739592,0.0010925366,0.010960941,0.0063787755,0.0018789177,0.031760514,0.0015452012],"about_ca_topic_score_codex":0.00060455,"about_ca_topic_score_gemma":0.0008610834,"teacher_disagreement_score":0.7684674,"about_ca_system_score_codex":0.00040576773,"about_ca_system_score_gemma":0.000017307526,"threshold_uncertainty_score":0.99996793},"labels":[],"label_agreement":null},{"id":"W4399661160","doi":"10.1159/000539520","title":"A statistical testing strategy accounting for random and non-random (skewed) X-chromosome inactivation identifies lung cancer susceptibility loci among smokers","year":2024,"lang":"en","type":"article","venue":"Human Heredity","topic":"Genetic Associations and Epidemiology","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":"Université de Montréal; McGill University Health Centre; Centre Hospitalier Universitaire Sainte-Justine","funders":"","keywords":"Lung cancer; Biology; Genetics; Lung cancer susceptibility; Cancer; Epidemiology; Incidence (geometry); Chromosome; Oncology; Internal medicine; Medicine; Genotype; Gene; Single-nucleotide polymorphism","score_opus":0.027410547315358608,"score_gpt":0.3282602608525392,"score_spread":0.3008497135371806,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4399661160","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9780525,0.0006375561,0.02009797,0.000055911398,0.0002886732,0.00050215056,0.00014957864,0.000031733343,0.00018392444],"genre_scores_gemma":[0.9977344,0.000045408196,0.0006804458,0.000032452732,0.00076858996,0.00016565737,0.00033754198,0.000024330455,0.00021113286],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9985851,0.00011092546,0.00036984825,0.0005153956,0.00010195827,0.00031675887],"domain_scores_gemma":[0.9990925,0.0003803625,0.000116176256,0.00017391122,0.00016776855,0.000069253714],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00090292934,0.00017747661,0.00027461268,0.000039724608,0.0003141612,0.00012070459,0.0000869263,0.00020706856,0.00005846711],"category_scores_gemma":[0.00092212425,0.00016939783,0.00007442052,0.000083000945,0.00017780108,0.000017926972,0.00007101583,0.00015074594,0.0000011242623],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0001711696,0.000066280416,0.75454605,0.0007014271,0.00031536064,0.000005169092,0.00024920888,0.0006390667,0.21969527,0.00014878398,0.019302621,0.004159596],"study_design_scores_gemma":[0.002592841,0.00022662993,0.9677811,0.00010584914,0.00018734655,0.0000046397568,0.00030650973,0.021660602,0.0036749674,0.0025649287,0.00048530623,0.0004092338],"about_ca_topic_score_codex":0.0008705554,"about_ca_topic_score_gemma":0.001155161,"teacher_disagreement_score":0.2160203,"about_ca_system_score_codex":0.000067662,"about_ca_system_score_gemma":0.00011151333,"threshold_uncertainty_score":0.69078434},"labels":[],"label_agreement":null}]}