{"meta":{"page":1,"per_page":50,"max_per_page":100,"total":836,"total_is_capped":false,"direct_labels_cover":0,"predictions_cover":836,"direct_label_status":"direct model label, unvalidated","prediction_status":"machine_predicted_unvalidated (Codex and Gemma teacher distillation)","score_status":"score_only:v0-immature-baseline (scores rank; they never assert a category)","snapshot":{"source":"OpenAlex, pinned release, all 482 partitions","release":"2026-06-24","frame_built":"2026-07-12"},"query_hash":"d376f43186a1","filters":{"venue":"The American Journal of Human Genetics"}},"results":[{"id":"W2150111967","doi":"10.1086/375033","title":"Average Risks of Breast and Ovarian Cancer Associated with BRCA1 or BRCA2 Mutations Detected in Case Series Unselected for Family History: A Combined Analysis of 22 Studies","year":2003,"lang":"en","type":"review","venue":"The American Journal of Human Genetics","topic":"BRCA gene mutations in cancer","field":"Biochemistry, Genetics and Molecular Biology","cited_by":3685,"is_retracted":false,"has_abstract":false,"routes":{"ca_aff":true,"ca_fund":false,"ca_venue":false,"about_ca":false},"ca_institutions":"Coalition for Research in Women's Health; University of Toronto","funders":"National Cancer Institute","keywords":"Breast cancer; Ovarian cancer; Family history; Medicine; Germline mutation; Oncology; Cancer; Context (archaeology); Relative risk; Internal medicine; Incidence (geometry); Mutation; BRCA mutation; Gynecology; Confidence interval; Genetics; Biology; Gene","retraction":null,"screen_n_in":null,"score":{"opus":0.0737969457601159,"gpt":0.3703780233766856,"spread":0.2965810776165697,"validation_status":"score_only:v0-immature-baseline"},"prediction":{"model_version":"codex-gemma-dda1882f352a","candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0004086623,0.0003119092,0.001740387,0.00046442,0.00009067771,0.00001004966,0.0002589737,0.0001011334,0.00000696292],"category_scores_gemma":[0.0001349771,0.0002118854,0.0002698349,0.001177471,0.0008551553,0.000004662331,0.00004414243,0.0002116189,1.764988e-8],"about_ca_system_candidate":false,"about_ca_system_consensus":false,"about_ca_system_score_codex":0.0003514444,"about_ca_system_score_gemma":0.00151522,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_topic_score_codex":0.0001183462,"about_ca_topic_score_gemma":0.002261755,"domain_scores_codex":[0.9978734,0.0005036129,0.0009826975,0.0002463766,0.000187735,0.0002061823],"domain_scores_gemma":[0.99553,0.0001870816,0.002865814,0.0003342298,0.001026544,0.00005633535],"domain_codex":null,"domain_gemma":null,"domain_candidate":null,"domain_consensus":null,"study_design_codex":"design_other","study_design_gemma":"meta_analysis","study_design_scores_codex":[0.005887744,0.001846912,0.00586812,0.008047661,0.2271368,0.0008166133,0.01416929,0.02881042,0.02128777,0.00006107262,0.003186469,0.6828811],"study_design_scores_gemma":[0.0384446,0.09572089,0.07928423,0.02927337,0.4150672,0.02811843,0.0373694,0.00138637,0.005919843,0.0005789775,0.257845,0.01099165],"study_design_candidate":"design_other","study_design_consensus":null,"genre_codex":"review","genre_gemma":"review","genre_scores_codex":[0.3659419,0.6330187,0.0001797893,0.00001218399,0.0000496937,0.0003664525,0.0004249246,0.000002182213,0.00000408814],"genre_scores_gemma":[0.2212214,0.777378,0.000964204,0.00002960472,0.0000424861,0.00007300255,0.000104731,0.00006076581,0.000125799],"genre_candidate":"review","genre_consensus":"review","teacher_disagreement_score":0.6718895,"threshold_uncertainty_score":0.8640438,"prediction_status":"machine_predicted_unvalidated"},"labels":[],"label_agreement":null},{"id":"W2521967673","doi":"10.1016/j.ajhg.2016.08.016","title":"REVEL: An Ensemble Method for Predicting the Pathogenicity of Rare Missense Variants","year":2016,"lang":"en","type":"article","venue":"The American Journal of Human Genetics","topic":"Genomics and Rare Diseases","field":"Biochemistry, Genetics and Molecular Biology","cited_by":2986,"is_retracted":false,"has_abstract":false,"routes":{"ca_aff":true,"ca_fund":false,"ca_venue":false,"about_ca":false},"ca_institutions":"Montreal General Hospital","funders":"National Human Genome Research Institute; National Institute of Mental Health; National Cancer Institute; National Institute for Health and Care Research; U.S. National Library of Medicine; Emory University","keywords":"Missense mutation; Pathogenicity; Genetics; Computational biology; Biology; Computer science; Mutation; Gene","retraction":null,"screen_n_in":null,"score":{"opus":0.01700784366975837,"gpt":0.3017367329907316,"spread":0.2847288893209732,"validation_status":"score_only:v0-immature-baseline"},"prediction":{"model_version":"codex-gemma-dda1882f352a","candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0007308469,0.00011381,0.0002138003,0.00002640884,0.0001454353,0.00001360937,0.0004643546,0.00002899657,0.000004820295],"category_scores_gemma":[0.0001290023,0.00005443282,0.0001858141,0.00005274854,0.0002124693,0.00000267081,0.00007421074,0.00005376467,2.644384e-7],"about_ca_system_candidate":false,"about_ca_system_consensus":false,"about_ca_system_score_codex":0.000007781879,"about_ca_system_score_gemma":0.0001104319,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_topic_score_codex":0.000006630474,"about_ca_topic_score_gemma":0.000008741461,"domain_scores_codex":[0.9989445,0.0002451419,0.000365701,0.0001345064,0.0001317477,0.0001783987],"domain_scores_gemma":[0.9983954,0.00009579721,0.0007104207,0.0004125995,0.0003003119,0.00008546381],"domain_codex":null,"domain_gemma":null,"domain_candidate":null,"domain_consensus":null,"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","study_design_scores_codex":[0.0002251215,0.0000494823,0.0006572137,0.000006274681,0.0001158546,0.000004363998,0.0001997005,0.00007784099,0.9762253,0.00003890981,0.0003863625,0.02201359],"study_design_scores_gemma":[0.002582208,0.01160992,0.04797399,0.0001397441,0.0008023501,0.001313254,0.00379477,0.0003191748,0.9182363,0.005337083,0.007301297,0.0005899736],"study_design_candidate":"bench_or_experimental","study_design_consensus":"bench_or_experimental","genre_codex":"empirical","genre_gemma":"empirical","genre_scores_codex":[0.9713155,0.0007943114,0.02734361,0.0002494079,0.00006987836,0.0001276284,0.00007245669,0.000001749598,0.00002544296],"genre_scores_gemma":[0.9903066,0.0002892111,0.008710167,0.0002085094,0.0003749299,0.000002738894,0.0000037604,0.00002381323,0.00008031841],"genre_candidate":"empirical","genre_consensus":"empirical","teacher_disagreement_score":0.05798905,"threshold_uncertainty_score":0.2219706,"prediction_status":"machine_predicted_unvalidated"},"labels":[],"label_agreement":null},{"id":"W2131587128","doi":"10.1016/j.ajhg.2010.04.006","title":"Consensus Statement: Chromosomal Microarray Is a First-Tier Clinical Diagnostic Test for Individuals with Developmental Disabilities or Congenital Anomalies","year":2010,"lang":"en","type":"review","venue":"The American Journal of Human Genetics","topic":"Genomic variations and chromosomal abnormalities","field":"Biochemistry, Genetics and Molecular Biology","cited_by":2873,"is_retracted":false,"has_abstract":false,"routes":{"ca_aff":true,"ca_fund":false,"ca_venue":false,"about_ca":false},"ca_institutions":"SickKids Foundation; Hospital for Sick Children; University of Toronto; Child and Family Research Institute; University of British Columbia","funders":"ARUP Laboratories; ACMG Foundation for Genetic and Genomic Medicine; Simons Foundation; National Institute of Mental Health; Eunice Kennedy Shriver National Institute of Child Health and Human Development; Howard Hughes Medical Institute","keywords":"Statement (logic); Test (biology); Microarray; Microarray analysis techniques; Intellectual disability; Medicine; Psychology; Genetics; Biology; Gene; Linguistics","retraction":null,"screen_n_in":null,"score":{"opus":0.03786928235145046,"gpt":0.3321678295130276,"spread":0.2942985471615772,"validation_status":"score_only:v0-immature-baseline"},"prediction":{"model_version":"codex-gemma-dda1882f352a","candidate_categories":["metaepi_narrow"],"consensus_categories":[],"category_scores_codex":[0.0006725357,0.0005337599,0.001402702,0.00008630127,0.0003673075,0.0001254485,0.0007742984,0.0001811163,0.00009359605],"category_scores_gemma":[0.0006961336,0.0003115745,0.0005309236,0.000117106,0.001814694,0.000005166028,0.0001986193,0.0004193203,0.000007518566],"about_ca_system_candidate":false,"about_ca_system_consensus":false,"about_ca_system_score_codex":0.00006154473,"about_ca_system_score_gemma":0.001269447,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_topic_score_codex":0.000007208113,"about_ca_topic_score_gemma":0.0001465274,"domain_scores_codex":[0.9969835,0.000226091,0.001685431,0.0003709697,0.0002624805,0.0004715548],"domain_scores_gemma":[0.9954331,0.001619839,0.002009785,0.0004450875,0.0003136302,0.0001785448],"domain_codex":null,"domain_gemma":null,"domain_candidate":null,"domain_consensus":null,"study_design_codex":"design_other","study_design_gemma":"not_applicable","study_design_scores_codex":[0.001580161,0.00351269,0.09525079,0.008872156,0.02011906,0.0001871694,0.01206506,0.0000382142,0.0009527921,0.0001210449,0.0362576,0.8210433],"study_design_scores_gemma":[0.0009030586,0.005920718,0.0004481233,0.0006437684,0.001528198,0.001784568,0.002995214,3.798184e-7,0.0003071175,0.00003153695,0.9848613,0.0005759787],"study_design_candidate":"not_applicable","study_design_consensus":null,"genre_codex":"empirical","genre_gemma":"review","genre_scores_codex":[0.575659,0.4213642,0.00003439898,0.00009398434,0.0002235571,0.0008526464,0.001722582,0.000005841238,0.00004381262],"genre_scores_gemma":[0.05271843,0.9352075,0.008952952,0.0002126356,0.001410294,0.0001332642,0.0002194435,0.0001441,0.001001387],"genre_candidate":"review","genre_consensus":null,"teacher_disagreement_score":0.9486037,"threshold_uncertainty_score":0.9999337,"prediction_status":"machine_predicted_unvalidated"},"labels":[],"label_agreement":null},{"id":"W2119907069","doi":"10.1016/j.ajhg.2007.12.009","title":"Structural Variation of Chromosomes in Autism Spectrum Disorder","year":2008,"lang":"en","type":"article","venue":"The American Journal of Human Genetics","topic":"Genomic variations and chromosomal abnormalities","field":"Biochemistry, Genetics and Molecular Biology","cited_by":1843,"is_retracted":false,"has_abstract":false,"routes":{"ca_aff":true,"ca_fund":false,"ca_venue":false,"about_ca":false},"ca_institutions":"Holland Bloorview Kids Rehabilitation Hospital; University of Alberta; McMaster University; North York General Hospital; Western University; Hospital for Sick Children; University of British Columbia; Memorial University of Newfoundland; Centre for Addiction and Mental Health; SickKids Foundation; University of Toronto","funders":"Autism Speaks","keywords":"Copy-number variation; Genetics; Autism spectrum disorder; Gene duplication; Biology; Structural variation; Autism; Microarray; Segmental duplication; Gene dosage; Single-nucleotide polymorphism; Gene; Genome; Genotype; Medicine; Gene family; Psychiatry","retraction":null,"screen_n_in":null,"score":{"opus":0.008810459800998462,"gpt":0.230564531301595,"spread":0.2217540715005965,"validation_status":"score_only:v0-immature-baseline"},"prediction":{"model_version":"codex-gemma-dda1882f352a","candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0001369047,0.00008994904,0.0001912513,0.00006064387,0.00008250204,0.000006257713,0.000240308,0.00002381314,0.00002494988],"category_scores_gemma":[0.00001023665,0.00006613413,0.00007989333,0.0001030778,0.0002522256,0.000003683609,0.00005005,0.00008418157,6.820914e-7],"about_ca_system_candidate":false,"about_ca_system_consensus":false,"about_ca_system_score_codex":0.00001508777,"about_ca_system_score_gemma":0.00008344049,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_topic_score_codex":0.00006974339,"about_ca_topic_score_gemma":0.00004081658,"domain_scores_codex":[0.999175,0.00008453804,0.0004037988,0.00007800616,0.0001271775,0.0001314815],"domain_scores_gemma":[0.9992078,0.00001077462,0.0005240004,0.0001856092,0.00004216547,0.00002964369],"domain_codex":null,"domain_gemma":null,"domain_candidate":null,"domain_consensus":null,"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","study_design_scores_codex":[0.0002873105,0.0002195965,0.3576851,0.00002742453,0.0003663588,0.00002958952,0.008104298,0.01559137,0.6120457,0.002672942,0.0001946709,0.002775625],"study_design_scores_gemma":[0.0005719169,0.001546314,0.9749403,0.00001062395,0.00002899543,0.0003411397,0.0006335313,0.00007300259,0.01963901,0.001769796,0.0003087082,0.0001366669],"study_design_candidate":"observational","study_design_consensus":null,"genre_codex":"empirical","genre_gemma":"empirical","genre_scores_codex":[0.998794,0.0005812678,0.0002016467,0.0002246386,0.00006854688,0.00004773716,0.000006295055,0.000001172742,0.00007469652],"genre_scores_gemma":[0.9988061,0.0003565425,0.0005520631,0.00004407227,0.0001452516,8.906466e-7,0.00000497803,0.00001063822,0.00007942595],"genre_candidate":"empirical","genre_consensus":"empirical","teacher_disagreement_score":0.6172552,"threshold_uncertainty_score":0.2696872,"prediction_status":"machine_predicted_unvalidated"},"labels":[],"label_agreement":null},{"id":"W2598022332","doi":"10.1016/j.ajhg.2017.03.004","title":"Human Demographic History Impacts Genetic Risk Prediction across Diverse Populations","year":2017,"lang":"en","type":"article","venue":"The American Journal of Human Genetics","topic":"Genetic Associations and Epidemiology","field":"Biochemistry, Genetics and Molecular Biology","cited_by":1561,"is_retracted":false,"has_abstract":false,"routes":{"ca_aff":true,"ca_fund":true,"ca_venue":false,"about_ca":false},"ca_institutions":"McGill University; McGill University and Génome Québec Innovation Centre; McGill Genome Centre","funders":"National Human Genome Research Institute; Canadian Institutes of Health Research; National Institute of General Medical Sciences; National Institute of Mental Health; Directorate for Mathematical and Physical Sciences; Canada Research Chairs; National Institutes of Health; National Science Foundation","keywords":"Genome-wide association study; Linkage disequilibrium; Genetic association; Population; Genetic architecture; Demographic history; Coalescent theory; Genomics; Biology; Evolutionary biology; Genetics; Quantitative trait locus; Demography; Allele; Genetic variation; Genome; Single-nucleotide polymorphism; Haplotype","retraction":null,"screen_n_in":null,"score":{"opus":0.0347765881824811,"gpt":0.3260201435870368,"spread":0.2912435554045557,"validation_status":"score_only:v0-immature-baseline"},"prediction":{"model_version":"codex-gemma-dda1882f352a","candidate_categories":["sts"],"consensus_categories":[],"category_scores_codex":[0.0008262751,0.0001834878,0.0003181759,0.00006786487,0.001306909,0.00004731848,0.0007848612,0.00008537906,0.00001875856],"category_scores_gemma":[0.0002304918,0.0001446899,0.0002655943,0.00004844166,0.0009328508,0.000007194053,0.0002016822,0.0002686539,0.000003868404],"about_ca_system_candidate":false,"about_ca_system_consensus":false,"about_ca_system_score_codex":0.00007615526,"about_ca_system_score_gemma":0.00008177237,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_topic_score_codex":0.0002297286,"about_ca_topic_score_gemma":0.000357074,"domain_scores_codex":[0.9983165,0.0003186087,0.0005998121,0.0002055169,0.0002053429,0.0003542713],"domain_scores_gemma":[0.9962451,0.00001768643,0.002462655,0.0008663885,0.0002562623,0.0001519368],"domain_codex":null,"domain_gemma":null,"domain_candidate":null,"domain_consensus":null,"study_design_codex":"observational","study_design_gemma":"observational","study_design_scores_codex":[0.00002743861,0.00006123898,0.9573869,0.000002873907,0.0001932021,0.000003992202,0.0003321823,0.001357421,0.02926353,0.00001438956,0.005717644,0.005639225],"study_design_scores_gemma":[0.0004432515,0.001364486,0.9939048,0.000009105452,0.0001604714,0.00005780512,0.000379644,0.00007679415,0.0001941733,0.0006346461,0.002627609,0.0001472208],"study_design_candidate":"observational","study_design_consensus":"observational","genre_codex":"empirical","genre_gemma":"empirical","genre_scores_codex":[0.9971738,0.001228002,0.000770012,0.0001493478,0.0003862178,0.0001046835,0.00004037253,0.000005708141,0.0001418903],"genre_scores_gemma":[0.9963963,0.0008687312,0.00156387,0.0001648066,0.0007783808,0.000003634488,0.00001412483,0.00002805902,0.0001821062],"genre_candidate":"empirical","genre_consensus":"empirical","teacher_disagreement_score":0.03651793,"threshold_uncertainty_score":0.9999933,"prediction_status":"machine_predicted_unvalidated"},"labels":[],"label_agreement":null},{"id":"W2901952863","doi":"10.1016/j.ajhg.2018.11.002","title":"Polygenic Risk Scores for Prediction of Breast Cancer and Breast Cancer Subtypes","year":2018,"lang":"en","type":"article","venue":"The American Journal of Human Genetics","topic":"Genetic Associations and Epidemiology","field":"Biochemistry, Genetics and Molecular Biology","cited_by":1183,"is_retracted":false,"has_abstract":false,"routes":{"ca_aff":true,"ca_fund":true,"ca_venue":false,"about_ca":false},"ca_institutions":"University of British Columbia; University Health Network; Sinai Health System; Public Health Ontario; Université Laval; Centre Hospitalier de l’Université de Montréal; Simon Fraser University; McGill University; Royal Victoria Hospital; Centre hospitalier universitaire de Québec; BC Cancer Agency; Queen's University; Mount Sinai Hospital; Lunenfeld-Tanenbaum Research Institute; University of Toronto","funders":"Canadian Institutes of Health Research; Horizon 2020 Framework Programme; National Institutes of Health; Ministero dello Sviluppo Economico; Fondazione Italiana per la Ricerca sul Cancro; Medical Research Council; Leids Universitair Medisch Centrum; Karolinska Institutet; University of California, San Diego; Oulun Yliopisto; University of Toronto; Queen's University; University of Melbourne; Monash University; National Cancer Institute; Universität Heidelberg; Curtin University of Technology; Deutsches Krebsforschungszentrum; Hunter Medical Research Institute; European Commission; University of Oxford; King's College London; Mailman School of Public Health, Columbia University; Seventh Framework Programme; Queen's University Belfast; University College London; Wellcome Trust; Cancer Research UK; University of Southampton; Memorial Sloan-Kettering Cancer Center; Fondation du cancer du sein du Québec; Génome Québec; National Institute for Health and Care Research; Ministère du Développement Économique, de l’Innovation et de l’Exportation; Genome Canada; Universiteit Leiden; Biocenter, University of Oulu; Government of Canada; Institut National de la Santé et de la Recherche Médicale; Ministère de l'Économie, de la Science et de l'Innovation - Québec; Wayne State University; Health Sciences Center, University of New Mexico; Case Western Reserve University","keywords":"Breast cancer; Polygenic risk score; Oncology; Cancer; Medicine; Internal medicine; Biology; Genetics; Gene; Genotype; Single-nucleotide polymorphism","retraction":null,"screen_n_in":null,"score":{"opus":0.0114559861583164,"gpt":0.2884326431659777,"spread":0.2769766570076613,"validation_status":"score_only:v0-immature-baseline"},"prediction":{"model_version":"codex-gemma-dda1882f352a","candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0003710174,0.00010356,0.0002411849,0.00004290946,0.0001487739,0.000007903194,0.0001842512,0.00004345295,0.00001521311],"category_scores_gemma":[0.00002787394,0.00007239348,0.00009463454,0.00007244296,0.0005963115,0.000002316061,0.00005016365,0.00007437797,2.54289e-7],"about_ca_system_candidate":false,"about_ca_system_consensus":false,"about_ca_system_score_codex":0.00001657363,"about_ca_system_score_gemma":0.0001030097,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_topic_score_codex":0.0002159043,"about_ca_topic_score_gemma":0.0001919838,"domain_scores_codex":[0.9991592,0.0001055467,0.0003436964,0.0001265578,0.00008989444,0.0001751146],"domain_scores_gemma":[0.9984614,0.00003231077,0.0008630333,0.0001740904,0.0004088174,0.00006038844],"domain_codex":null,"domain_gemma":null,"domain_candidate":null,"domain_consensus":null,"study_design_codex":"observational","study_design_gemma":"observational","study_design_scores_codex":[0.0003087091,0.00003688227,0.8309199,0.000008640015,0.0003610376,1.239456e-7,0.0002025816,0.0001941629,0.1394278,0.00000993817,0.002415637,0.02611458],"study_design_scores_gemma":[0.0004024961,0.001214244,0.9932158,0.00001751405,0.0001917759,0.00007536177,0.0002026813,0.0001321471,0.003826415,0.0002591134,0.0003875989,0.00007487607],"study_design_candidate":"observational","study_design_consensus":"observational","genre_codex":"empirical","genre_gemma":"empirical","genre_scores_codex":[0.9957514,0.002172706,0.0006187134,0.0005565647,0.0001388229,0.00008976383,0.0006593294,0.000001657372,0.00001105155],"genre_scores_gemma":[0.993663,0.00436483,0.0006782439,0.0001449076,0.00106633,0.000007329185,0.000005657939,0.00001613594,0.000053566],"genre_candidate":"empirical","genre_consensus":"empirical","teacher_disagreement_score":0.1622958,"threshold_uncertainty_score":0.295212,"prediction_status":"machine_predicted_unvalidated"},"labels":[],"label_agreement":null},{"id":"W2147024435","doi":"10.1086/376549","title":"Genome Scan Meta-Analysis of Schizophrenia and Bipolar Disorder, Part II: Schizophrenia","year":2003,"lang":"en","type":"article","venue":"The American Journal of Human Genetics","topic":"Genetic Associations and Epidemiology","field":"Biochemistry, Genetics and Molecular Biology","cited_by":1146,"is_retracted":false,"has_abstract":false,"routes":{"ca_aff":true,"ca_fund":false,"ca_venue":false,"about_ca":false},"ca_institutions":"University of Toronto; Xenon Pharmaceuticals (Canada)","funders":"National Institute of Mental Health; Wellcome Trust","keywords":"Schizophrenia (object-oriented programming); Bipolar disorder; Meta-analysis; Psychiatry; Psychology; Genome Scan; Medicine; Genetics; Biology; Cognition; Gene; Internal medicine; Allele","retraction":null,"screen_n_in":null,"score":{"opus":0.02517983480943577,"gpt":0.2792826354137395,"spread":0.2541028006043038,"validation_status":"score_only:v0-immature-baseline"},"prediction":{"model_version":"codex-gemma-dda1882f352a","candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0008482226,0.0001839302,0.000886193,0.0001887323,0.0001862702,0.00001226207,0.0003124098,0.00005404568,0.0001211494],"category_scores_gemma":[0.0001136387,0.0001262663,0.0005741791,0.0003809989,0.0005021688,0.000002122338,0.0000954268,0.0001292772,0.000001128564],"about_ca_system_candidate":false,"about_ca_system_consensus":false,"about_ca_system_score_codex":0.000008252236,"about_ca_system_score_gemma":0.00007106833,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_topic_score_codex":0.00002029397,"about_ca_topic_score_gemma":0.0001018951,"domain_scores_codex":[0.998318,0.0004609276,0.000624404,0.0001979209,0.000167206,0.0002315923],"domain_scores_gemma":[0.9980943,0.00004399614,0.001141717,0.0004454686,0.0001648363,0.0001097273],"domain_codex":null,"domain_gemma":null,"domain_candidate":null,"domain_consensus":null,"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","study_design_scores_codex":[0.0005557241,0.0007399091,0.2190325,0.00002591016,0.3045125,0.000008890675,0.001020165,0.01647611,0.4397165,0.002144706,0.001532145,0.01423498],"study_design_scores_gemma":[0.002449817,0.008266781,0.704848,0.000007192125,0.1719532,0.0001682862,0.001424301,0.0001582724,0.01002785,0.002255565,0.09736636,0.001074343],"study_design_candidate":"observational","study_design_consensus":null,"genre_codex":"empirical","genre_gemma":"empirical","genre_scores_codex":[0.9749925,0.02397604,0.000589897,0.0001496644,0.00003026452,0.00007274495,0.00002167839,0.000002137027,0.0001650723],"genre_scores_gemma":[0.9929479,0.002079135,0.004349265,0.0001207033,0.00007972,0.000003139636,0.000008723478,0.00002813683,0.0003832302],"genre_candidate":"empirical","genre_consensus":"empirical","teacher_disagreement_score":0.4858155,"threshold_uncertainty_score":0.5148989,"prediction_status":"machine_predicted_unvalidated"},"labels":[],"label_agreement":null},{"id":"W2151135161","doi":"10.1086/503850","title":"Serotonin Transporter Promoter Gain-of-Function Genotypes Are Linked to Obsessive-Compulsive Disorder","year":2006,"lang":"en","type":"article","venue":"The American Journal of Human Genetics","topic":"Obsessive-Compulsive Spectrum Disorders","field":"Psychology","cited_by":1124,"is_retracted":false,"has_abstract":false,"routes":{"ca_aff":true,"ca_fund":false,"ca_venue":false,"about_ca":false},"ca_institutions":"University of Toronto; Centre for Addiction and Mental Health","funders":"National Institutes of Health; National Institute of Mental Health; University of Louisville","keywords":"Serotonin transporter; Obsessive compulsive; Genotype; Function (biology); Transporter; Serotonin Plasma Membrane Transport Proteins; Serotonin; Gain of function; Genetics; Biology; Psychology; Gene; Psychiatry; Mutation","retraction":null,"screen_n_in":null,"score":{"opus":0.01173812193954021,"gpt":0.2821036433442631,"spread":0.2703655214047229,"validation_status":"score_only:v0-immature-baseline"},"prediction":{"model_version":"codex-gemma-dda1882f352a","candidate_categories":["metaepi_narrow"],"consensus_categories":[],"category_scores_codex":[0.0002877449,0.0003418641,0.0007370662,0.0002999821,0.0001835026,0.00003596048,0.0007359832,0.00006612876,0.0004441614],"category_scores_gemma":[0.00001497066,0.0002538729,0.0003172892,0.000522873,0.0005876728,0.00005842206,0.00004707248,0.0004584464,0.00005834894],"about_ca_system_candidate":false,"about_ca_system_consensus":false,"about_ca_system_score_codex":0.00006053392,"about_ca_system_score_gemma":0.00006071803,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_topic_score_codex":0.0002024934,"about_ca_topic_score_gemma":0.0001483124,"domain_scores_codex":[0.9973518,0.0003587124,0.001036062,0.0003155381,0.0004558576,0.0004820819],"domain_scores_gemma":[0.9967563,0.0001114848,0.002017326,0.0005754713,0.0004093465,0.0001301412],"domain_codex":null,"domain_gemma":null,"domain_candidate":null,"domain_consensus":null,"study_design_codex":"observational","study_design_gemma":"observational","study_design_scores_codex":[0.004098884,0.003054642,0.7654428,0.0001076332,0.00231012,0.0003521305,0.02966561,0.02528388,0.06869268,0.002785837,0.007042195,0.09116355],"study_design_scores_gemma":[0.001340782,0.003312646,0.9847546,0.00007589174,0.0002879279,0.00006601619,0.004448249,0.00002633417,0.0008238714,0.002907988,0.001600294,0.0003554215],"study_design_candidate":"observational","study_design_consensus":"observational","genre_codex":"empirical","genre_gemma":"empirical","genre_scores_codex":[0.9893398,0.000973787,0.006909277,0.001052378,0.0004599339,0.0005288438,0.00001843264,0.00002275998,0.0006947871],"genre_scores_gemma":[0.9970879,0.00002110069,0.001426577,0.0005364852,0.0004861609,0.00001685707,0.000007826397,0.00007845378,0.0003386269],"genre_candidate":"empirical","genre_consensus":"empirical","teacher_disagreement_score":0.2193117,"threshold_uncertainty_score":0.9999914,"prediction_status":"machine_predicted_unvalidated"},"labels":[],"label_agreement":null},{"id":"W2129867386","doi":"10.1016/j.ajhg.2014.03.018","title":"Convergence of Genes and Cellular Pathways Dysregulated in Autism Spectrum Disorders","year":2014,"lang":"en","type":"article","venue":"The American Journal of Human Genetics","topic":"Genomic variations and chromosomal abnormalities","field":"Biochemistry, Genetics and Molecular Biology","cited_by":1028,"is_retracted":false,"has_abstract":true,"routes":{"ca_aff":true,"ca_fund":true,"ca_venue":false,"about_ca":false},"ca_institutions":"SickKids Foundation; Holland Bloorview Kids Rehabilitation Hospital; Memorial University of Newfoundland; University of Alberta; Lunenfeld-Tanenbaum Research Institute; Mount Sinai Hospital; Ontario Genomics; University of Toronto; Hospital for Sick Children; Cancer Care Ontario; McMaster University; Public Health Ontario","funders":"Eunice Kennedy Shriver National Institute of Child Health and Human Development; Hospital for Sick Children; National Institute of Mental Health; Medical Research Council; Ontario Genomics Institute; Wellcome Trust; National Alliance for Research on Schizophrenia and Depression; Health Research Board; Canadian Institutes of Health Research; National Institute of General Medical Sciences; National Institute for Health and Care Research; Genome Canada; Brain and Behavior Research Foundation","keywords":"Copy-number variation; Genetics; Autism; Gene; Biology; Intellectual disability; Single-nucleotide polymorphism; Autism spectrum disorder; Loss function; Phenotype; Medicine; Genome; Genotype; Psychiatry","retraction":null,"screen_n_in":null,"score":{"opus":0.005465712231729811,"gpt":0.2007686517389237,"spread":0.1953029395071939,"validation_status":"score_only:v0-immature-baseline"},"prediction":{"model_version":"codex-gemma-dda1882f352a","candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0002367236,0.00008934324,0.0001829368,0.0000474852,0.00005102621,0.000008695671,0.0002005425,0.00002427269,0.0000118773],"category_scores_gemma":[0.000006954979,0.00006836042,0.00005281629,0.00006978801,0.0003102951,0.000002187481,0.00006229231,0.00006555209,4.18305e-7],"about_ca_system_candidate":false,"about_ca_system_consensus":false,"about_ca_system_score_codex":0.000006009034,"about_ca_system_score_gemma":0.00003371261,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_topic_score_codex":0.00003895556,"about_ca_topic_score_gemma":0.00005804307,"domain_scores_codex":[0.9992777,0.0001079379,0.0003095922,0.0000878646,0.00008831623,0.0001285806],"domain_scores_gemma":[0.9993799,0.00001270801,0.0003653601,0.0001805494,0.00002238445,0.00003914331],"domain_codex":null,"domain_gemma":null,"domain_candidate":null,"domain_consensus":null,"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","study_design_scores_codex":[0.00005830439,0.00006223335,0.05052179,0.00001556533,0.00007492926,0.000001719956,0.000751072,0.001494318,0.9401411,0.002524251,0.00003089521,0.004323774],"study_design_scores_gemma":[0.00129947,0.004980586,0.2920937,0.00004513844,0.0001020591,0.000106032,0.001910259,0.0006772109,0.6789975,0.01699674,0.002380866,0.0004104801],"study_design_candidate":"bench_or_experimental","study_design_consensus":"bench_or_experimental","genre_codex":"empirical","genre_gemma":"empirical","genre_scores_codex":[0.997752,0.001153871,0.000736989,0.0001828784,0.00005233444,0.0000424155,0.000003626627,0.000001126477,0.00007481986],"genre_scores_gemma":[0.9988756,0.0006280622,0.0003431422,0.00004067451,0.00006731879,7.102191e-7,0.000002872063,0.00001027205,0.00003140804],"genre_candidate":"empirical","genre_consensus":"empirical","teacher_disagreement_score":0.2611436,"threshold_uncertainty_score":0.2787657,"prediction_status":"machine_predicted_unvalidated"},"labels":[],"label_agreement":null},{"id":"W2128371599","doi":"10.1016/j.ajhg.2013.06.020","title":"RFMix: A Discriminative Modeling Approach for Rapid and Robust Local-Ancestry Inference","year":2013,"lang":"en","type":"article","venue":"The American Journal of Human Genetics","topic":"Genetic and phenotypic traits in livestock","field":"Biochemistry, Genetics and Molecular Biology","cited_by":1023,"is_retracted":false,"has_abstract":false,"routes":{"ca_aff":true,"ca_fund":false,"ca_venue":false,"about_ca":false},"ca_institutions":"McGill University","funders":"U.S. National Library of Medicine; National Human Genome Research Institute","keywords":"Discriminative model; International HapMap Project; Genetic genealogy; Inference; Conditional random field; Random forest; 1000 Genomes Project; Parameterized complexity; Ancestry-informative marker; Biology; Artificial intelligence; Computer science; Evolutionary biology; Machine learning; Genetics; Genome; Human genome; Allele; Allele frequency; Algorithm; Demography; Population; Genotype; Gene","retraction":null,"screen_n_in":null,"score":{"opus":0.04188053889035954,"gpt":0.2855342987138907,"spread":0.2436537598235312,"validation_status":"score_only:v0-immature-baseline"},"prediction":{"model_version":"codex-gemma-dda1882f352a","candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0001800576,0.0001485489,0.0002204337,0.0000303077,0.0001352316,0.00003905861,0.0003387235,0.00003761861,0.00000739463],"category_scores_gemma":[0.00002606244,0.0001013181,0.00007888912,0.00005094095,0.0005708243,0.000005002254,0.00008607811,0.0001353423,4.967139e-7],"about_ca_system_candidate":false,"about_ca_system_consensus":false,"about_ca_system_score_codex":0.000007137022,"about_ca_system_score_gemma":0.00005804405,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_topic_score_codex":0.000010806,"about_ca_topic_score_gemma":0.000001812333,"domain_scores_codex":[0.9991393,0.00007731689,0.0002917328,0.0001658171,0.000123746,0.0002020917],"domain_scores_gemma":[0.9991038,0.0000284566,0.0003111441,0.0002217111,0.000239639,0.00009522315],"domain_codex":null,"domain_gemma":null,"domain_candidate":null,"domain_consensus":null,"study_design_codex":"simulation_or_modeling","study_design_gemma":"simulation_or_modeling","study_design_scores_codex":[0.0003625288,0.0003491043,0.001758518,0.0001052194,0.0005477557,7.264386e-7,0.004159252,0.6212944,0.09710667,0.002583037,0.001715411,0.2700174],"study_design_scores_gemma":[0.011343,0.07418825,0.1603228,0.0004234334,0.002186078,0.001141599,0.1151985,0.384677,0.08141149,0.161865,0.002182756,0.00506002],"study_design_candidate":"simulation_or_modeling","study_design_consensus":"simulation_or_modeling","genre_codex":"empirical","genre_gemma":"empirical","genre_scores_codex":[0.5637966,0.0008566204,0.4349797,0.00006485037,0.00002529366,0.0001238121,0.000003095772,0.000001413649,0.0001486435],"genre_scores_gemma":[0.8885279,0.0001738432,0.1108114,0.0001456598,0.0002396707,0.00001541404,0.000005250155,0.00001786928,0.00006297366],"genre_candidate":"empirical","genre_consensus":"empirical","teacher_disagreement_score":0.3247313,"threshold_uncertainty_score":0.4131634,"prediction_status":"machine_predicted_unvalidated"},"labels":[],"label_agreement":null},{"id":"W2025460005","doi":"10.1086/318787","title":"Prevalence and Penetrance of Germline BRCA1 and BRCA2 Mutations in a Population Series of 649 Women with Ovarian Cancer","year":2001,"lang":"en","type":"article","venue":"The American Journal of Human Genetics","topic":"BRCA gene mutations in cancer","field":"Biochemistry, Genetics and Molecular Biology","cited_by":992,"is_retracted":false,"has_abstract":false,"routes":{"ca_aff":true,"ca_fund":false,"ca_venue":false,"about_ca":false},"ca_institutions":"Women's College Hospital; University of Toronto; Lunenfeld-Tanenbaum Research Institute; Toronto Public Health","funders":"National Cancer Institute","keywords":"Penetrance; Ovarian cancer; Medicine; Cancer; Germline mutation; Oncology; First-degree relatives; Breast cancer; Population; Internal medicine; BRCA2 Protein; Gynecology; Mutation; Biology; Genetics; Family history; Gene; Phenotype","retraction":null,"screen_n_in":null,"score":{"opus":0.009833074886504513,"gpt":0.2782463689712086,"spread":0.268413294084704,"validation_status":"score_only:v0-immature-baseline"},"prediction":{"model_version":"codex-gemma-dda1882f352a","candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0001890703,0.00008321491,0.0001843204,0.00006627785,0.00004044487,0.000007776837,0.0001225963,0.00002036887,0.000009138871],"category_scores_gemma":[0.00001478763,0.00006377378,0.00001663767,0.0001576537,0.0004633007,0.000007462601,0.00002906634,0.00006767982,2.302032e-8],"about_ca_system_candidate":false,"about_ca_system_consensus":false,"about_ca_system_score_codex":0.0000286267,"about_ca_system_score_gemma":0.00009201187,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_topic_score_codex":0.00007846035,"about_ca_topic_score_gemma":0.0002163182,"domain_scores_codex":[0.9992891,0.00006640286,0.0003112839,0.0001055077,0.0001209232,0.0001068135],"domain_scores_gemma":[0.9991401,0.00001496613,0.0005070078,0.0001541153,0.0001479346,0.00003585413],"domain_codex":null,"domain_gemma":null,"domain_candidate":null,"domain_consensus":null,"study_design_codex":"observational","study_design_gemma":"observational","study_design_scores_codex":[0.0007256579,0.00006915187,0.6818795,0.00008314284,0.0001544991,0.000004234402,0.003531387,0.007018503,0.2872622,0.00003857016,0.00001447491,0.0192187],"study_design_scores_gemma":[0.0005650393,0.001480883,0.9832781,0.00006399223,0.00004598913,0.0001358026,0.0007332598,0.00003883355,0.01319049,0.0003080592,0.00007132274,0.00008823693],"study_design_candidate":"observational","study_design_consensus":"observational","genre_codex":"empirical","genre_gemma":"empirical","genre_scores_codex":[0.9968088,0.002707837,0.0001809254,0.000169475,0.00001704775,0.00008550667,0.00001295131,8.176413e-7,0.00001664303],"genre_scores_gemma":[0.9949716,0.003187299,0.001687459,0.00003985513,0.00005682645,0.000006712836,0.000001893177,0.00001153091,0.00003679534],"genre_candidate":"empirical","genre_consensus":"empirical","teacher_disagreement_score":0.3013986,"threshold_uncertainty_score":0.2600619,"prediction_status":"machine_predicted_unvalidated"},"labels":[],"label_agreement":null},{"id":"W1925825565","doi":"10.1016/j.ajhg.2015.05.022","title":"Points to Consider: Ethical, Legal, and Psychosocial Implications of Genetic Testing in Children and Adolescents","year":2015,"lang":"en","type":"review","venue":"The American Journal of Human Genetics","topic":"BRCA gene mutations in cancer","field":"Biochemistry, Genetics and Molecular Biology","cited_by":898,"is_retracted":false,"has_abstract":false,"routes":{"ca_aff":true,"ca_fund":false,"ca_venue":false,"about_ca":false},"ca_institutions":"University of Toronto; St. Michael's Hospital","funders":"National Center for Advancing Translational Sciences; National Human Genome Research Institute","keywords":"Psychosocial; Genetic testing; Medical genetics; Statement (logic); Engineering ethics; Test (biology); Medicine; Psychology; Political science; Genetics; Psychiatry; Biology; Law; Engineering","retraction":null,"screen_n_in":null,"score":{"opus":0.0426088248687867,"gpt":0.3854298743079599,"spread":0.3428210494391732,"validation_status":"score_only:v0-immature-baseline"},"prediction":{"model_version":"codex-gemma-dda1882f352a","candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0004992268,0.0002240935,0.0007662053,0.0001473463,0.00007334982,0.00003195352,0.0003978116,0.0001375175,0.000001165386],"category_scores_gemma":[0.000160439,0.0001782101,0.00009838471,0.000282906,0.0005987941,0.000001800465,0.0001954419,0.0004474851,6.684043e-7],"about_ca_system_candidate":false,"about_ca_system_consensus":false,"about_ca_system_score_codex":0.00005386935,"about_ca_system_score_gemma":0.0006076556,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_topic_score_codex":0.0000199649,"about_ca_topic_score_gemma":0.00002460379,"domain_scores_codex":[0.9983132,0.0003077393,0.0007679172,0.0002473969,0.0001789574,0.0001848039],"domain_scores_gemma":[0.9981033,0.00004717741,0.001053244,0.0003648498,0.0002961023,0.0001353385],"domain_codex":null,"domain_gemma":null,"domain_candidate":null,"domain_consensus":null,"study_design_codex":"design_other","study_design_gemma":"not_applicable","study_design_scores_codex":[0.0000231962,0.00006382747,0.009715991,0.0002784096,0.0002126547,0.000001853283,0.0002017852,0.00003838655,0.00101644,0.00001236037,0.001941097,0.986494],"study_design_scores_gemma":[0.004333108,0.01280093,0.4514539,0.01723348,0.004912934,0.006321873,0.0009927195,0.000008825857,0.000527054,0.004173058,0.4941505,0.003091627],"study_design_candidate":"design_other","study_design_consensus":null,"genre_codex":"review","genre_gemma":"review","genre_scores_codex":[0.3035231,0.6957777,0.00007282136,0.0002028223,0.00003935999,0.0003321781,0.00003607037,0.000001455264,0.00001446678],"genre_scores_gemma":[0.1032001,0.8890189,0.006963797,0.0003916044,0.000345507,0.00001339751,0.000007479554,0.00005343079,0.000005720965],"genre_candidate":"review","genre_consensus":"review","teacher_disagreement_score":0.9834024,"threshold_uncertainty_score":0.7267197,"prediction_status":"machine_predicted_unvalidated"},"labels":[],"label_agreement":null},{"id":"W1983044117","doi":"10.1016/j.ajhg.2011.06.001","title":"VPS35 Mutations in Parkinson Disease","year":2011,"lang":"en","type":"article","venue":"The American Journal of Human Genetics","topic":"Parkinson's Disease Mechanisms and Treatments","field":"Medicine","cited_by":893,"is_retracted":false,"has_abstract":false,"routes":{"ca_aff":true,"ca_fund":false,"ca_venue":false,"about_ca":false},"ca_institutions":"University of Saskatchewan; Saskatchewan Health Authority; University of British Columbia","funders":"National Institute of Neurological Disorders and Stroke","keywords":"Disease; Parkinson's disease; Genetics; Medicine; Biology; Internal medicine","retraction":null,"screen_n_in":null,"score":{"opus":0.03627026363995609,"gpt":0.2970246533970576,"spread":0.2607543897571015,"validation_status":"score_only:v0-immature-baseline"},"prediction":{"model_version":"codex-gemma-dda1882f352a","candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0001355548,0.0001004255,0.0002325992,0.0001326653,0.00006393248,0.000008157498,0.0001390312,0.000009241146,0.0000885346],"category_scores_gemma":[0.00001800344,0.00006548366,0.00011269,0.0001648929,0.000174012,0.00002560254,0.00002068689,0.0001251363,0.00001076906],"about_ca_system_candidate":false,"about_ca_system_consensus":false,"about_ca_system_score_codex":0.0000487668,"about_ca_system_score_gemma":0.000106183,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_topic_score_codex":0.00003610682,"about_ca_topic_score_gemma":0.000009590053,"domain_scores_codex":[0.9991877,0.00007472446,0.0002752751,0.00008810435,0.0002157552,0.0001584058],"domain_scores_gemma":[0.9991403,0.0000198772,0.0003057885,0.000222481,0.00007680148,0.0002347157],"domain_codex":null,"domain_gemma":null,"domain_candidate":null,"domain_consensus":null,"study_design_codex":"observational","study_design_gemma":"observational","study_design_scores_codex":[0.002132113,0.002660691,0.9050443,0.00003166919,0.0005824621,0.002960235,0.005589664,0.00009035685,0.003724939,0.0009361328,0.000507853,0.07573958],"study_design_scores_gemma":[0.001009862,0.001276365,0.9897029,0.00005165175,0.0003432476,0.00008075843,0.0006182385,0.00004403291,0.0007510457,0.004109569,0.001936723,0.00007557502],"study_design_candidate":"observational","study_design_consensus":"observational","genre_codex":"empirical","genre_gemma":"empirical","genre_scores_codex":[0.9981688,0.0008004155,0.0001099575,0.0001641073,0.00004543229,0.0001048557,0.000007670974,0.000005873143,0.0005929391],"genre_scores_gemma":[0.9978402,0.0001983492,0.001498637,0.0002978584,0.00008384201,0.000004299618,0.000003030976,0.00001694396,0.00005679253],"genre_candidate":"empirical","genre_consensus":"empirical","teacher_disagreement_score":0.08465862,"threshold_uncertainty_score":0.2670346,"prediction_status":"machine_predicted_unvalidated"},"labels":[],"label_agreement":null},{"id":"W2121471393","doi":"10.1016/j.ajhg.2008.01.008","title":"Epigenomic Profiling Reveals DNA-Methylation Changes Associated with Major Psychosis","year":2008,"lang":"en","type":"article","venue":"The American Journal of Human Genetics","topic":"Epigenetics and DNA Methylation","field":"Biochemistry, Genetics and Molecular Biology","cited_by":776,"is_retracted":false,"has_abstract":false,"routes":{"ca_aff":true,"ca_fund":false,"ca_venue":false,"about_ca":false},"ca_institutions":"Université Laval; Centre for Addiction and Mental Health","funders":"National Institute of Mental Health","keywords":"Epigenomics; DNA methylation; Psychosis; Profiling (computer programming); Computational biology; Biology; Genetics; Medicine; Psychiatry; Computer science; Gene; Gene expression","retraction":null,"screen_n_in":null,"score":{"opus":0.02233375735204721,"gpt":0.2790641784117239,"spread":0.2567304210596766,"validation_status":"score_only:v0-immature-baseline"},"prediction":{"model_version":"codex-gemma-dda1882f352a","candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0005780658,0.0001678969,0.0002743499,0.0000880052,0.0002529341,0.00002018172,0.000299306,0.00005186932,0.000006804115],"category_scores_gemma":[0.00006473952,0.0001178974,0.00009414021,0.0001893843,0.0002646771,0.00000340697,0.00004096275,0.0001494279,0.000001825115],"about_ca_system_candidate":false,"about_ca_system_consensus":false,"about_ca_system_score_codex":0.00003041137,"about_ca_system_score_gemma":0.00006394136,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_topic_score_codex":0.00000608001,"about_ca_topic_score_gemma":0.00003170151,"domain_scores_codex":[0.9987129,0.0002366587,0.0003737091,0.0001740991,0.0002698617,0.0002327732],"domain_scores_gemma":[0.9982585,0.00004026444,0.0009943844,0.0003090697,0.0003102935,0.0000874972],"domain_codex":null,"domain_gemma":null,"domain_candidate":null,"domain_consensus":null,"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","study_design_scores_codex":[0.000102366,0.00005436776,0.02469736,0.000003201774,0.0001661016,0.000004777821,0.0002498381,0.000387949,0.9710109,0.000009260968,0.0001079698,0.003205887],"study_design_scores_gemma":[0.0008343673,0.005472532,0.1861196,0.00004304612,0.0001590646,0.00006059491,0.0002834806,0.00003144226,0.8053657,0.0004314668,0.0008717744,0.0003268796],"study_design_candidate":"bench_or_experimental","study_design_consensus":"bench_or_experimental","genre_codex":"empirical","genre_gemma":"empirical","genre_scores_codex":[0.9958709,0.002285003,0.001248947,0.0002298368,0.00007252959,0.0001498762,0.000007366402,0.000005180013,0.0001303966],"genre_scores_gemma":[0.9961836,0.001446627,0.001601167,0.0001521127,0.0003965238,0.00000498357,0.00002168271,0.00003815009,0.000155124],"genre_candidate":"empirical","genre_consensus":"empirical","teacher_disagreement_score":0.1656452,"threshold_uncertainty_score":0.4807716,"prediction_status":"machine_predicted_unvalidated"},"labels":[],"label_agreement":null},{"id":"W2005817756","doi":"10.1086/522590","title":"Contribution of SHANK3 Mutations to Autism Spectrum Disorder","year":2007,"lang":"en","type":"article","venue":"The American Journal of Human Genetics","topic":"Autism Spectrum Disorder Research","field":"Neuroscience","cited_by":691,"is_retracted":false,"has_abstract":false,"routes":{"ca_aff":true,"ca_fund":false,"ca_venue":false,"about_ca":false},"ca_institutions":"McMaster University; University of Alberta; Memorial University of Newfoundland; Centre for Addiction and Mental Health; University of Toronto; SickKids Foundation; Genome Canada; Ontario Genomics; Hospital for Sick Children","funders":"National Institute of Mental Health","keywords":"Autism spectrum disorder; Heritability of autism; Spectrum (functional analysis); Autism; Genetics; Psychology; Medicine; Psychiatry; Biology; Physics","retraction":null,"screen_n_in":null,"score":{"opus":0.0220220659091312,"gpt":0.3346176753005334,"spread":0.3125956093914022,"validation_status":"score_only:v0-immature-baseline"},"prediction":{"model_version":"codex-gemma-dda1882f352a","candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0008408873,0.0001213048,0.0002844257,0.0002968377,0.0002319897,0.00003188958,0.0006934231,0.00001830721,0.00008511123],"category_scores_gemma":[0.0002470635,0.00009106089,0.000109694,0.0008298659,0.0006769358,0.00005342782,0.0001144098,0.0002928325,0.00002547591],"about_ca_system_candidate":false,"about_ca_system_consensus":false,"about_ca_system_score_codex":0.00007190183,"about_ca_system_score_gemma":0.0000841174,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_topic_score_codex":0.00004002008,"about_ca_topic_score_gemma":0.00008044623,"domain_scores_codex":[0.9979722,0.0001929712,0.0006183778,0.0001500063,0.0006459331,0.0004204968],"domain_scores_gemma":[0.9984851,0.0003063624,0.0006921016,0.0003131496,0.00004528264,0.0001580257],"domain_codex":null,"domain_gemma":null,"domain_candidate":null,"domain_consensus":null,"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","study_design_scores_codex":[0.000443996,0.0005446014,0.01381511,0.000009931655,0.00006593061,0.0001049667,0.005224555,0.002482229,0.846411,0.1118149,0.0002170942,0.0188657],"study_design_scores_gemma":[0.001276249,0.006418361,0.3798012,0.00005128522,0.00008549771,0.0003844989,0.001332051,0.0002518205,0.5068728,0.1012761,0.001875808,0.0003742733],"study_design_candidate":"bench_or_experimental","study_design_consensus":"bench_or_experimental","genre_codex":"empirical","genre_gemma":"empirical","genre_scores_codex":[0.9739524,0.0001424504,0.0174411,0.007826624,0.00008403495,0.0002037163,0.00000787145,0.00001065209,0.0003311508],"genre_scores_gemma":[0.9990885,0.00007230776,0.0003755907,0.0002994469,0.00006830901,0.000001402855,5.379527e-7,0.00002139722,0.00007254427],"genre_candidate":"empirical","genre_consensus":"empirical","teacher_disagreement_score":0.3659861,"threshold_uncertainty_score":0.3713355,"prediction_status":"machine_predicted_unvalidated"},"labels":[],"label_agreement":null},{"id":"W2124032562","doi":"10.1086/342975","title":"Mutations in the O-Mannosyltransferase Gene POMT1 Give Rise to the Severe Neuronal Migration Disorder Walker-Warburg Syndrome","year":2002,"lang":"en","type":"article","venue":"The American Journal of Human Genetics","topic":"Muscle Physiology and Disorders","field":"Biochemistry, Genetics and Molecular Biology","cited_by":688,"is_retracted":false,"has_abstract":false,"routes":{"ca_aff":true,"ca_fund":false,"ca_venue":false,"about_ca":false},"ca_institutions":"University of Toronto","funders":"National Institute of Neurological Disorders and Stroke; Nederlandse Organisatie voor Wetenschappelijk Onderzoek","keywords":"Congenital muscular dystrophy; Genetics; Biology; Disease gene identification; Missense mutation; Nonsense mutation; Gene; Muscular dystrophy; Candidate gene; Locus (genetics); Frameshift mutation; Mutation; Exome sequencing","retraction":null,"screen_n_in":null,"score":{"opus":0.01031003134969316,"gpt":0.2462691263058555,"spread":0.2359590949561624,"validation_status":"score_only:v0-immature-baseline"},"prediction":{"model_version":"codex-gemma-dda1882f352a","candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0002682472,0.0001496324,0.0001660713,0.0000559771,0.0002646293,0.00002808931,0.000598776,0.00003304924,0.00004249957],"category_scores_gemma":[0.00003385553,0.00008310684,0.000126911,0.0002222065,0.0003266914,0.000005134539,0.00004247223,0.0002425267,0.00001091017],"about_ca_system_candidate":false,"about_ca_system_consensus":false,"about_ca_system_score_codex":0.000008152391,"about_ca_system_score_gemma":0.00002832357,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_topic_score_codex":0.00003559478,"about_ca_topic_score_gemma":0.000209207,"domain_scores_codex":[0.9987203,0.0004010116,0.0003159149,0.0001546436,0.0001909316,0.0002171728],"domain_scores_gemma":[0.9992386,0.00006041731,0.0001922603,0.000370473,0.00008208019,0.00005617836],"domain_codex":null,"domain_gemma":null,"domain_candidate":null,"domain_consensus":null,"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","study_design_scores_codex":[0.001348519,0.002164988,0.03174583,0.00003451941,0.0008480003,0.0001750944,0.03092748,0.2199258,0.6180691,0.0002648759,0.03315239,0.06134348],"study_design_scores_gemma":[0.003928469,0.01947498,0.8905649,0.00006105276,0.00057919,0.002478139,0.01843166,0.001942554,0.01274772,0.00349895,0.0448908,0.001401607],"study_design_candidate":"observational","study_design_consensus":null,"genre_codex":"empirical","genre_gemma":"empirical","genre_scores_codex":[0.9925272,0.001063817,0.0005758061,0.005475393,0.00006489107,0.0001972888,0.00001505725,0.000002302341,0.00007819507],"genre_scores_gemma":[0.9968131,0.0005474284,0.0001043156,0.002271235,0.0001538443,0.00001259908,0.00001321405,0.0000160995,0.00006812909],"genre_candidate":"empirical","genre_consensus":"empirical","teacher_disagreement_score":0.8588191,"threshold_uncertainty_score":0.3388999,"prediction_status":"machine_predicted_unvalidated"},"labels":[],"label_agreement":null},{"id":"W2156190275","doi":"10.1086/507318","title":"Mutations in the CEP290 (NPHP6) Gene Are a Frequent Cause of Leber Congenital Amaurosis","year":2006,"lang":"en","type":"article","venue":"The American Journal of Human Genetics","topic":"Retinal Development and Disorders","field":"Biochemistry, Genetics and Molecular Biology","cited_by":676,"is_retracted":false,"has_abstract":false,"routes":{"ca_aff":true,"ca_fund":false,"ca_venue":false,"about_ca":false},"ca_institutions":"McGill University Health Centre","funders":"Nederlandse Organisatie voor Wetenschappelijk Onderzoek","keywords":"Genetics; Exon; Mutation; Gene; Biology; Allele; Blindness; RNA splicing; Splice site mutation; Point mutation; Medicine; RNA; Alternative splicing","retraction":null,"screen_n_in":null,"score":{"opus":0.01125680564929398,"gpt":0.2571851063299452,"spread":0.2459283006806512,"validation_status":"score_only:v0-immature-baseline"},"prediction":{"model_version":"codex-gemma-dda1882f352a","candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0002467359,0.0001127154,0.0001765191,0.00006288605,0.00007706165,0.00002104319,0.0003644183,0.00002457256,0.000008805157],"category_scores_gemma":[0.0000214025,0.0000708218,0.0001101949,0.0001561245,0.0003862136,0.000002788665,0.00003958584,0.000107631,0.00000135261],"about_ca_system_candidate":false,"about_ca_system_consensus":false,"about_ca_system_score_codex":0.00001151397,"about_ca_system_score_gemma":0.00006911669,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_topic_score_codex":0.00006719595,"about_ca_topic_score_gemma":0.000205627,"domain_scores_codex":[0.9989969,0.0001397298,0.0003971031,0.00009480066,0.0002144682,0.0001570393],"domain_scores_gemma":[0.9990497,0.00002608144,0.000546827,0.0002130643,0.0001364689,0.00002782199],"domain_codex":null,"domain_gemma":null,"domain_candidate":null,"domain_consensus":null,"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","study_design_scores_codex":[0.0001866073,0.0003394737,0.2714503,0.00001094988,0.0002276108,0.00004327956,0.00155346,0.002382898,0.7190339,0.0001346016,0.002809303,0.00182764],"study_design_scores_gemma":[0.00105879,0.001554064,0.8854755,0.0000227626,0.0001634977,0.0002051122,0.005025397,0.0000198671,0.1026724,0.001700857,0.001806128,0.0002956259],"study_design_candidate":"observational","study_design_consensus":null,"genre_codex":"empirical","genre_gemma":"empirical","genre_scores_codex":[0.9979393,0.001088238,0.00016395,0.0003274275,0.0000374229,0.00008997237,0.000008383682,0.00000114447,0.0003441511],"genre_scores_gemma":[0.9988024,0.0002259816,0.0005335524,0.0002192333,0.0001183455,0.000003768936,0.00001340037,0.0000129408,0.00007036242],"genre_candidate":"empirical","genre_consensus":"empirical","teacher_disagreement_score":0.6163615,"threshold_uncertainty_score":0.2888029,"prediction_status":"machine_predicted_unvalidated"},"labels":[],"label_agreement":null},{"id":"W2035172439","doi":"10.1086/342288","title":"The Brain-Derived Neurotrophic Factor Gene Confers Susceptibility to Bipolar Disorder: Evidence from a Family-Based Association Study","year":2002,"lang":"en","type":"article","venue":"The American Journal of Human Genetics","topic":"Bipolar Disorder and Treatment","field":"Medicine","cited_by":595,"is_retracted":false,"has_abstract":false,"routes":{"ca_aff":true,"ca_fund":false,"ca_venue":false,"about_ca":false},"ca_institutions":"Centre for Addiction and Mental Health","funders":"National Institute of Mental Health; National Institutes of Health","keywords":"Brain-derived neurotrophic factor; Bipolar disorder; Association (psychology); Neurotrophic factors; Psychology; Gene; Genetics; Clinical psychology; Medicine; Oncology; Neuroscience; Biology; Cognition; Psychotherapist; Receptor","retraction":null,"screen_n_in":null,"score":{"opus":0.04043980033229128,"gpt":0.3000513413758062,"spread":0.259611541043515,"validation_status":"score_only:v0-immature-baseline"},"prediction":{"model_version":"codex-gemma-dda1882f352a","candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0004608369,0.000217684,0.0004564667,0.00007730864,0.0003912581,0.00007537649,0.0003969442,0.00002787862,0.00006045811],"category_scores_gemma":[0.000309357,0.0001250633,0.0002088961,0.0002678103,0.0002197074,0.00003368276,0.00005666365,0.0003686461,0.00002192595],"about_ca_system_candidate":false,"about_ca_system_consensus":false,"about_ca_system_score_codex":0.0002205035,"about_ca_system_score_gemma":0.00009176646,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_topic_score_codex":0.0003181319,"about_ca_topic_score_gemma":0.0004062438,"domain_scores_codex":[0.9975806,0.000641239,0.0005347823,0.0002217921,0.0007142597,0.0003073294],"domain_scores_gemma":[0.997515,0.0006831894,0.0006652265,0.000627803,0.0003110718,0.000197706],"domain_codex":null,"domain_gemma":null,"domain_candidate":null,"domain_consensus":null,"study_design_codex":"observational","study_design_gemma":"observational","study_design_scores_codex":[0.0002938262,0.0007907083,0.8885538,0.000003789258,0.0004705435,0.00001693981,0.003450246,0.0001473481,0.08105945,5.702482e-7,0.0001936812,0.02501908],"study_design_scores_gemma":[0.00142769,0.008100492,0.9863775,0.00002998206,0.0004088047,0.000007010445,0.001453347,0.0002086261,0.000860841,0.00002814009,0.0009684372,0.0001291594],"study_design_candidate":"observational","study_design_consensus":"observational","genre_codex":"empirical","genre_gemma":"empirical","genre_scores_codex":[0.9835564,0.009284816,0.0003476616,0.0060065,0.0001049623,0.0006574971,0.00001805234,0.000016321,0.00000772047],"genre_scores_gemma":[0.9973923,0.000956566,0.0002908863,0.001113344,0.0001573813,0.000009767022,0.000001615364,0.00003115078,0.00004696882],"genre_candidate":"empirical","genre_consensus":"empirical","teacher_disagreement_score":0.09782364,"threshold_uncertainty_score":0.5099933,"prediction_status":"machine_predicted_unvalidated"},"labels":[],"label_agreement":null},{"id":"W2117950559","doi":"10.1086/376547","title":"Genome Scan Meta-Analysis of Schizophrenia and Bipolar Disorder, Part III: Bipolar Disorder","year":2003,"lang":"en","type":"review","venue":"The American Journal of Human Genetics","topic":"Genetic Associations and Epidemiology","field":"Biochemistry, Genetics and Molecular Biology","cited_by":572,"is_retracted":false,"has_abstract":false,"routes":{"ca_aff":true,"ca_fund":false,"ca_venue":false,"about_ca":false},"ca_institutions":"Montreal General Hospital; University of Ottawa; Dalhousie University; Centre hospitalier de l'Université Laval; McGill University","funders":"National Institute of Neurological Disorders and Stroke; National Human Genome Research Institute; National Institute of Mental Health; National Center for Research Resources; Wellcome Trust","keywords":"Bipolar disorder; Schizophrenia (object-oriented programming); Psychiatry; Psychology; Meta-analysis; Medicine; Internal medicine; Lithium (medication)","retraction":null,"screen_n_in":null,"score":{"opus":0.04514264617115781,"gpt":0.3261144753027246,"spread":0.2809718291315668,"validation_status":"score_only:v0-immature-baseline"},"prediction":{"model_version":"codex-gemma-dda1882f352a","candidate_categories":["metaepi_narrow"],"consensus_categories":[],"category_scores_codex":[0.001221892,0.0004810824,0.003821341,0.0004177787,0.0001702353,0.00002413106,0.0006906118,0.0001829812,0.0001402936],"category_scores_gemma":[0.0000842437,0.0003084024,0.00222175,0.0007030826,0.0007147326,0.000002241468,0.0001860088,0.0003333208,0.000002656913],"about_ca_system_candidate":false,"about_ca_system_consensus":false,"about_ca_system_score_codex":0.00002088312,"about_ca_system_score_gemma":0.000193977,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_topic_score_codex":0.00004658876,"about_ca_topic_score_gemma":0.0001358212,"domain_scores_codex":[0.9962941,0.001131274,0.001580985,0.0003770909,0.0002504869,0.0003660874],"domain_scores_gemma":[0.9948456,0.0001040279,0.003874388,0.0008183408,0.0002006778,0.0001569701],"domain_codex":null,"domain_gemma":null,"domain_candidate":null,"domain_consensus":null,"study_design_codex":"design_other","study_design_gemma":"not_applicable","study_design_scores_codex":[0.00005668516,0.0003768295,0.005333131,0.0005255879,0.4029134,0.000006680278,0.0001907456,0.001024181,0.0006031012,0.00009025243,0.0007937317,0.5880857],"study_design_scores_gemma":[0.0001748601,0.0006934752,0.001185253,0.00002380542,0.1484841,0.00003986201,0.00007537624,0.000003973999,0.000003805687,0.00003186892,0.8489889,0.0002947642],"study_design_candidate":"not_applicable","study_design_consensus":null,"genre_codex":"review","genre_gemma":"review","genre_scores_codex":[0.03302903,0.9659961,0.0005137905,0.00003318884,0.00005111682,0.0002250331,0.000105749,0.00000250948,0.00004344985],"genre_scores_gemma":[0.002994621,0.9946944,0.001288944,0.00006964737,0.0001584695,0.00001313965,0.00007545012,0.00008715365,0.0006182439],"genre_candidate":"review","genre_consensus":"review","teacher_disagreement_score":0.8481951,"threshold_uncertainty_score":0.9999368,"prediction_status":"machine_predicted_unvalidated"},"labels":[],"label_agreement":null},{"id":"W2103089222","doi":"10.1086/498651","title":"Replication of Putative Candidate-Gene Associations with Rheumatoid Arthritis in >4,000 Samples from North America and Sweden: Association of Susceptibility with PTPN22, CTLA4, and PADI4","year":2005,"lang":"en","type":"article","venue":"The American Journal of Human Genetics","topic":"Cytokine Signaling Pathways and Interactions","field":"Medicine","cited_by":561,"is_retracted":false,"has_abstract":false,"routes":{"ca_aff":true,"ca_fund":false,"ca_venue":false,"about_ca":false},"ca_institutions":"Université de Montréal; Montreal Heart Institute","funders":"National Institute of Arthritis and Musculoskeletal and Skin Diseases; National Institutes of Health; Broad Institute; National Institute of Allergy and Infectious Diseases; Abbott Laboratories","keywords":"PTPN22; Replication (statistics); Rheumatoid arthritis; Candidate gene; Genetics; Gene; Biology; Association (psychology); Computational biology; Evolutionary biology; Medicine; Genotype; Single-nucleotide polymorphism; Immunology; Virology; Psychology","retraction":null,"screen_n_in":null,"score":{"opus":0.01484659420790665,"gpt":0.2717562664032445,"spread":0.2569096721953378,"validation_status":"score_only:v0-immature-baseline"},"prediction":{"model_version":"codex-gemma-dda1882f352a","candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0003089058,0.0001123896,0.000510072,0.0001148942,0.00007602634,0.00001501187,0.00007294807,0.00002248127,0.00001468972],"category_scores_gemma":[0.0001407519,0.00007651876,0.00004222342,0.000247617,0.0003106221,0.00006589374,0.00001894375,0.0002107544,1.897718e-7],"about_ca_system_candidate":false,"about_ca_system_consensus":false,"about_ca_system_score_codex":0.0001316421,"about_ca_system_score_gemma":0.0001149491,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_topic_score_codex":0.001083248,"about_ca_topic_score_gemma":0.003013035,"domain_scores_codex":[0.9986987,0.0001413538,0.000581369,0.0001603774,0.0002959737,0.0001222998],"domain_scores_gemma":[0.997219,0.0002846248,0.00173944,0.0002471324,0.0004404138,0.00006938328],"domain_codex":null,"domain_gemma":null,"domain_candidate":null,"domain_consensus":null,"study_design_codex":"observational","study_design_gemma":"observational","study_design_scores_codex":[0.0003809021,0.0002302611,0.8652928,0.000007911605,0.0003060569,0.000002519917,0.006654197,0.0006861242,0.1044384,0.000007617966,0.00004374367,0.02194946],"study_design_scores_gemma":[0.001241032,0.002689332,0.9689732,0.0001140891,0.0001183014,0.0000420161,0.002079919,0.0001358507,0.02432226,0.00006666438,0.0001290878,0.00008822073],"study_design_candidate":"observational","study_design_consensus":"observational","genre_codex":"empirical","genre_gemma":"empirical","genre_scores_codex":[0.998049,0.0004915153,0.0004028702,0.0006191985,0.0000082806,0.0001555621,0.0002439556,0.000004141616,0.00002549541],"genre_scores_gemma":[0.9946427,0.001393824,0.003757421,0.000070116,0.00005468073,0.000003293461,0.00005746887,0.00001352308,0.000006976581],"genre_candidate":"empirical","genre_consensus":"empirical","teacher_disagreement_score":0.1036805,"threshold_uncertainty_score":0.3120344,"prediction_status":"machine_predicted_unvalidated"},"labels":[],"label_agreement":null},{"id":"W2038502254","doi":"10.1086/316954","title":"Usher Syndrome 1D and Nonsyndromic Autosomal Recessive Deafness DFNB12 Are Caused by Allelic Mutations of the Novel Cadherin-Like Gene CDH23","year":2001,"lang":"en","type":"article","venue":"The American Journal of Human Genetics","topic":"Hearing, Cochlea, Tinnitus, Genetics","field":"Neuroscience","cited_by":557,"is_retracted":false,"has_abstract":false,"routes":{"ca_aff":true,"ca_fund":false,"ca_venue":false,"about_ca":false},"ca_institutions":"McGill University","funders":"National Institute on Deafness and Other Communication Disorders; National Institutes of Health","keywords":"Genetics; Frameshift mutation; Biology; Missense mutation; Locus (genetics); Nonsense mutation; Retinitis pigmentosa; Nonsense; Usher syndrome; Gene; Allele; Exon; Mutation","retraction":null,"screen_n_in":null,"score":{"opus":0.03333613752787665,"gpt":0.284156426106535,"spread":0.2508202885786583,"validation_status":"score_only:v0-immature-baseline"},"prediction":{"model_version":"codex-gemma-dda1882f352a","candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.000343681,0.00029196,0.0005394055,0.0001403799,0.0004407883,0.00008722669,0.001120345,0.0000602093,0.00004827373],"category_scores_gemma":[0.0001418717,0.0002064435,0.0001451826,0.0006326498,0.001482686,0.00007865756,0.0002808952,0.0005190079,0.000007622217],"about_ca_system_candidate":false,"about_ca_system_consensus":false,"about_ca_system_score_codex":0.00008088702,"about_ca_system_score_gemma":0.000211497,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_topic_score_codex":0.0000797956,"about_ca_topic_score_gemma":0.00005788472,"domain_scores_codex":[0.9973758,0.0003705064,0.0007972901,0.0003231092,0.0006636301,0.0004696775],"domain_scores_gemma":[0.9969908,0.0002330581,0.001671417,0.0006793722,0.0002189314,0.0002064405],"domain_codex":null,"domain_gemma":null,"domain_candidate":null,"domain_consensus":null,"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","study_design_scores_codex":[0.00003855658,0.0001888902,0.01461648,0.00001551916,0.00007631461,0.0001100124,0.00180214,0.002147058,0.979117,0.00001937499,0.0003182152,0.001550482],"study_design_scores_gemma":[0.002438229,0.002413209,0.7901237,0.0002089037,0.0004340698,0.01069898,0.003309152,0.0008691028,0.1851099,0.000399893,0.003150229,0.0008446064],"study_design_candidate":"bench_or_experimental","study_design_consensus":null,"genre_codex":"empirical","genre_gemma":"empirical","genre_scores_codex":[0.9979234,0.0003862794,0.0003817947,0.0006701263,0.000258333,0.0002591201,0.00003482297,0.00001644139,0.00006971036],"genre_scores_gemma":[0.9977565,0.0004424981,0.0005786094,0.0006562349,0.00008692668,0.000005204028,8.717151e-7,0.00006766947,0.0004054894],"genre_candidate":"empirical","genre_consensus":"empirical","teacher_disagreement_score":0.794007,"threshold_uncertainty_score":0.8418522,"prediction_status":"machine_predicted_unvalidated"},"labels":[],"label_agreement":null},{"id":"W2011308707","doi":"10.1086/340731","title":"Recurrent Mutation of the Gene Encoding sequestosome 1 (SQSTM1/p62) in Paget Disease of Bone","year":2002,"lang":"en","type":"article","venue":"The American Journal of Human Genetics","topic":"Bone health and treatments","field":"Medicine","cited_by":556,"is_retracted":false,"has_abstract":false,"routes":{"ca_aff":true,"ca_fund":true,"ca_venue":false,"about_ca":false},"ca_institutions":"Centre hospitalier de l'Université Laval","funders":"Fonds de Recherche du Québec - Santé; Canadian Institutes of Health Research; Fonds pour la Formation de Chercheurs et l'Aide à la Recherche; Canada Foundation for Innovation","keywords":"Sequestosome 1; Paget's disease of bone; Mutation; Gene; Disease; Medicine; Genetics; Biology; Internal medicine","retraction":null,"screen_n_in":null,"score":{"opus":0.04005552714101837,"gpt":0.3168062267785633,"spread":0.276750699637545,"validation_status":"score_only:v0-immature-baseline"},"prediction":{"model_version":"codex-gemma-dda1882f352a","candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0002341934,0.00009221525,0.000350698,0.0001126623,0.00004999991,0.000003133622,0.0001168547,0.00001302302,0.00002219713],"category_scores_gemma":[0.00006343087,0.00005293256,0.0001156514,0.0002348091,0.0002572038,0.0000200021,0.00002588478,0.0001809348,0.000001259826],"about_ca_system_candidate":false,"about_ca_system_consensus":false,"about_ca_system_score_codex":0.00008440932,"about_ca_system_score_gemma":0.00009686818,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_topic_score_codex":0.00003439822,"about_ca_topic_score_gemma":0.00001046083,"domain_scores_codex":[0.9987003,0.0001520465,0.0005962973,0.00007091873,0.0003287041,0.0001517688],"domain_scores_gemma":[0.9984692,0.00005249849,0.0009520599,0.0002539785,0.0001406999,0.0001315724],"domain_codex":null,"domain_gemma":null,"domain_candidate":null,"domain_consensus":null,"study_design_codex":"observational","study_design_gemma":"observational","study_design_scores_codex":[0.002152744,0.003508898,0.6806023,0.0005601472,0.0005208335,0.0006750445,0.0147027,0.001541788,0.05193613,0.0002223355,0.001038615,0.2425384],"study_design_scores_gemma":[0.002801475,0.003975742,0.9787714,0.0005667317,0.0004882037,0.0003208324,0.0006274399,0.0005405824,0.0104886,0.001166557,0.0001290085,0.0001233925],"study_design_candidate":"observational","study_design_consensus":"observational","genre_codex":"empirical","genre_gemma":"empirical","genre_scores_codex":[0.9948955,0.003651618,0.0000127038,0.001091461,0.00007530172,0.0001800888,0.000007568642,0.000002075599,0.00008371246],"genre_scores_gemma":[0.9983603,0.0009758848,0.0003588438,0.0001830689,0.00005884031,0.000002103866,0.000001331435,0.00001204185,0.00004753546],"genre_candidate":"empirical","genre_consensus":"empirical","teacher_disagreement_score":0.2981691,"threshold_uncertainty_score":0.2158527,"prediction_status":"machine_predicted_unvalidated"},"labels":[],"label_agreement":null},{"id":"W1985764154","doi":"10.1086/426403","title":"CHEK2 Is a Multiorgan Cancer Susceptibility Gene","year":2004,"lang":"en","type":"article","venue":"The American Journal of Human Genetics","topic":"BRCA gene mutations in cancer","field":"Biochemistry, Genetics and Molecular Biology","cited_by":555,"is_retracted":false,"has_abstract":false,"routes":{"ca_aff":true,"ca_fund":false,"ca_venue":false,"about_ca":false},"ca_institutions":"Coalition for Research in Women's Health","funders":"","keywords":"CHEK2; Multiorgan failure; Gene; Genetics; Medicine; Biology; Internal medicine; Mutation","retraction":null,"screen_n_in":null,"score":{"opus":0.01598810311857032,"gpt":0.3159356584831712,"spread":0.2999475553646009,"validation_status":"score_only:v0-immature-baseline"},"prediction":{"model_version":"codex-gemma-dda1882f352a","candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0002816324,0.0001544866,0.00021677,0.00004789412,0.000148932,0.00002633418,0.0005163221,0.00004033513,0.00005088652],"category_scores_gemma":[0.00002426558,0.000116746,0.0001546712,0.0001688133,0.0005599737,0.000003090777,0.00009611157,0.0001743367,0.000005720469],"about_ca_system_candidate":false,"about_ca_system_consensus":false,"about_ca_system_score_codex":0.0001482583,"about_ca_system_score_gemma":0.0004178889,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_topic_score_codex":0.0000738732,"about_ca_topic_score_gemma":0.0001483464,"domain_scores_codex":[0.998885,0.00007627815,0.0003799269,0.000196253,0.0002380988,0.0002243955],"domain_scores_gemma":[0.9985507,0.000008882848,0.0005249082,0.0005029443,0.0003188273,0.00009377894],"domain_codex":null,"domain_gemma":null,"domain_candidate":null,"domain_consensus":null,"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","study_design_scores_codex":[0.00007768466,0.00007807053,0.005692188,0.000004594278,0.0001774673,0.000003739856,0.00101751,0.003782056,0.9771789,0.000008945837,0.001156022,0.01082281],"study_design_scores_gemma":[0.0009786632,0.001511463,0.03979714,0.00001730958,0.0001186883,0.0001304918,0.000742613,0.00000912235,0.9502193,0.0007405316,0.00548648,0.000248162],"study_design_candidate":"bench_or_experimental","study_design_consensus":"bench_or_experimental","genre_codex":"empirical","genre_gemma":"empirical","genre_scores_codex":[0.9952049,0.002171069,0.001130223,0.001132201,0.000170907,0.0000975199,0.00001707804,0.000004233182,0.00007183044],"genre_scores_gemma":[0.9932644,0.0008690594,0.003679854,0.00126496,0.0007757121,0.000005773046,0.000003848652,0.00003262165,0.0001037153],"genre_candidate":"empirical","genre_consensus":"empirical","teacher_disagreement_score":0.03410495,"threshold_uncertainty_score":0.4760762,"prediction_status":"machine_predicted_unvalidated"},"labels":[],"label_agreement":null},{"id":"W2026686051","doi":"10.1086/320121","title":"Mortality in Neurofibromatosis 1: An Analysis Using U.S. Death Certificates","year":2001,"lang":"en","type":"article","venue":"The American Journal of Human Genetics","topic":"Neurofibromatosis and Schwannoma Cases","field":"Medicine","cited_by":536,"is_retracted":false,"has_abstract":false,"routes":{"ca_aff":true,"ca_fund":false,"ca_venue":false,"about_ca":false},"ca_institutions":"University of British Columbia","funders":"","keywords":"Neurofibromatosis; Medicine; Pathology","retraction":null,"screen_n_in":null,"score":{"opus":0.08332837679835389,"gpt":0.351753937745289,"spread":0.2684255609469351,"validation_status":"score_only:v0-immature-baseline"},"prediction":{"model_version":"codex-gemma-dda1882f352a","candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0004023159,0.0001656933,0.0006829861,0.0004077055,0.00011256,0.00005179279,0.0002784312,0.00002121078,0.00004853954],"category_scores_gemma":[0.0000256838,0.0001121645,0.0002852716,0.0009802169,0.0002460726,0.00007375493,0.00004017757,0.000226515,0.000001655224],"about_ca_system_candidate":false,"about_ca_system_consensus":false,"about_ca_system_score_codex":0.00004693691,"about_ca_system_score_gemma":0.00006044205,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_topic_score_codex":0.0001894248,"about_ca_topic_score_gemma":0.00003057702,"domain_scores_codex":[0.9981924,0.0002724273,0.0007073458,0.0001814237,0.0003899173,0.000256507],"domain_scores_gemma":[0.9984241,0.00006295148,0.000656859,0.0005318501,0.0001324292,0.0001918788],"domain_codex":null,"domain_gemma":null,"domain_candidate":null,"domain_consensus":null,"study_design_codex":"observational","study_design_gemma":"observational","study_design_scores_codex":[0.0001250739,0.0002172387,0.9168075,0.000005806898,0.0002616351,0.0004221349,0.0002508619,0.001289526,0.07977083,0.00001524732,0.00001111332,0.0008230819],"study_design_scores_gemma":[0.00034368,0.001492258,0.9864565,0.00002650475,0.001352129,0.001203828,0.0006394179,0.002915137,0.00530761,0.0001074591,0.0000370504,0.0001183867],"study_design_candidate":"observational","study_design_consensus":"observational","genre_codex":"empirical","genre_gemma":"empirical","genre_scores_codex":[0.9992025,0.0002813465,0.0001143625,0.0002128026,0.00003433467,0.00008427201,0.000002899306,0.00001079743,0.0000566892],"genre_scores_gemma":[0.9985215,0.0001605911,0.0009039647,0.0002524412,0.0001229589,7.953918e-7,0.000002402782,0.00002555812,0.000009807412],"genre_candidate":"empirical","genre_consensus":"empirical","teacher_disagreement_score":0.07446322,"threshold_uncertainty_score":0.4573937,"prediction_status":"machine_predicted_unvalidated"},"labels":[],"label_agreement":null},{"id":"W2078288169","doi":"10.1016/j.ajhg.2009.05.005","title":"Genomic and Genic Deletions of the FOX Gene Cluster on 16q24.1 and Inactivating Mutations of FOXF1 Cause Alveolar Capillary Dysplasia and Other Malformations","year":2009,"lang":"en","type":"article","venue":"The American Journal of Human Genetics","topic":"Congenital Diaphragmatic Hernia Studies","field":"Medicine","cited_by":536,"is_retracted":false,"has_abstract":true,"routes":{"ca_aff":true,"ca_fund":false,"ca_venue":false,"about_ca":false},"ca_institutions":"McMaster University","funders":"Wellcome Trust","keywords":"Haploinsufficiency; Genetics; Biology; Candidate gene; Frameshift mutation; Gene; Phenotype","retraction":null,"screen_n_in":null,"score":{"opus":0.01665712609510826,"gpt":0.2788744829192623,"spread":0.262217356824154,"validation_status":"score_only:v0-immature-baseline"},"prediction":{"model_version":"codex-gemma-dda1882f352a","candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0002165827,0.0001131982,0.0003198367,0.0001123421,0.0001832264,0.00001114007,0.00008888961,0.00001906736,0.000006309834],"category_scores_gemma":[0.00007602028,0.00006929172,0.00006092723,0.000130783,0.0005284399,0.00002971146,0.00005533696,0.0001671253,3.337852e-7],"about_ca_system_candidate":false,"about_ca_system_consensus":false,"about_ca_system_score_codex":0.00002700443,"about_ca_system_score_gemma":0.00004872716,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_topic_score_codex":0.00001595433,"about_ca_topic_score_gemma":0.00002183644,"domain_scores_codex":[0.9990709,0.00009878015,0.0004558767,0.00007268404,0.0001859508,0.0001158363],"domain_scores_gemma":[0.9988491,0.0001767253,0.0005825363,0.0001980353,0.0001393941,0.00005418604],"domain_codex":null,"domain_gemma":null,"domain_candidate":null,"domain_consensus":null,"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","study_design_scores_codex":[0.0004447101,0.000469045,0.275574,0.0002166745,0.002087953,0.00001646012,0.04714805,0.0008729487,0.6136772,0.0006770375,0.000339424,0.05847652],"study_design_scores_gemma":[0.0009424335,0.001625331,0.98712,0.0001267834,0.0006093348,0.0005577151,0.00368891,0.0003530875,0.004035776,0.0007535891,0.00008935694,0.00009762288],"study_design_candidate":"observational","study_design_consensus":null,"genre_codex":"empirical","genre_gemma":"empirical","genre_scores_codex":[0.9965876,0.001811076,0.00009604025,0.001105953,0.00001562542,0.0002129498,0.00001300422,0.000002805481,0.0001549148],"genre_scores_gemma":[0.9977615,0.0003853322,0.001252343,0.0005275849,0.00003650328,0.000001690755,5.557668e-7,0.00001284373,0.00002168321],"genre_candidate":"empirical","genre_consensus":"empirical","teacher_disagreement_score":0.7115461,"threshold_uncertainty_score":0.2825634,"prediction_status":"machine_predicted_unvalidated"},"labels":[],"label_agreement":null},{"id":"W2002079712","doi":"10.1086/510560","title":"A Comprehensive Analysis of Common Copy-Number Variations in the Human Genome","year":2006,"lang":"en","type":"article","venue":"The American Journal of Human Genetics","topic":"Genomic variations and chromosomal abnormalities","field":"Biochemistry, Genetics and Molecular Biology","cited_by":522,"is_retracted":false,"has_abstract":false,"routes":{"ca_aff":true,"ca_fund":false,"ca_venue":false,"about_ca":false},"ca_institutions":"BC Cancer Agency; University of British Columbia","funders":"","keywords":"Human genome; Biology; Genome; Copy-number variation; Computational biology; Evolutionary biology; Genetics; Gene","retraction":null,"screen_n_in":null,"score":{"opus":0.01125730664579707,"gpt":0.2721943051339589,"spread":0.2609369984881618,"validation_status":"score_only:v0-immature-baseline"},"prediction":{"model_version":"codex-gemma-dda1882f352a","candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0002698328,0.0001052951,0.0002989716,0.0001064815,0.0001440697,0.00002476024,0.0004522712,0.0000257548,0.00003195353],"category_scores_gemma":[0.000003883207,0.00006923595,0.0001951918,0.000388387,0.0002756431,0.000002584619,0.00005755895,0.0001126911,0.000001048247],"about_ca_system_candidate":false,"about_ca_system_consensus":false,"about_ca_system_score_codex":0.00001594683,"about_ca_system_score_gemma":0.00003783029,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_topic_score_codex":0.0003182162,"about_ca_topic_score_gemma":0.0002741595,"domain_scores_codex":[0.9988294,0.0002522878,0.0005170397,0.00008909746,0.0001711092,0.0001410756],"domain_scores_gemma":[0.9987666,0.00003949401,0.0006631634,0.0003362473,0.0001732198,0.00002126317],"domain_codex":null,"domain_gemma":null,"domain_candidate":null,"domain_consensus":null,"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","study_design_scores_codex":[0.00007411911,0.0006345591,0.3701822,0.00001577772,0.001934083,0.00001377914,0.003697757,0.04109186,0.5763302,0.005077073,0.0005967528,0.0003518046],"study_design_scores_gemma":[0.0003295695,0.0005811219,0.9893021,0.000004652326,0.0006482708,0.00004970955,0.002261349,0.00005132467,0.003680954,0.001178785,0.001784231,0.0001279483],"study_design_candidate":"observational","study_design_consensus":null,"genre_codex":"empirical","genre_gemma":"empirical","genre_scores_codex":[0.9985677,0.0002727297,0.0003469338,0.0001336891,0.00001867883,0.00006847853,0.00002880997,0.000001073722,0.000561878],"genre_scores_gemma":[0.9991535,0.00005591001,0.0003321822,0.0001798737,0.0001548353,0.000002753791,0.00005036891,0.000009268478,0.00006132686],"genre_candidate":"empirical","genre_consensus":"empirical","teacher_disagreement_score":0.6191199,"threshold_uncertainty_score":0.282336,"prediction_status":"machine_predicted_unvalidated"},"labels":[],"label_agreement":null},{"id":"W2030222772","doi":"10.1086/511888","title":"Mutations in Cohesin Complex Members SMC3 and SMC1A Cause a Mild Variant of Cornelia de Lange Syndrome with Predominant Mental Retardation","year":2007,"lang":"en","type":"article","venue":"The American Journal of Human Genetics","topic":"Genomics and Chromatin Dynamics","field":"Biochemistry, Genetics and Molecular Biology","cited_by":522,"is_retracted":false,"has_abstract":false,"routes":{"ca_aff":true,"ca_fund":false,"ca_venue":false,"about_ca":false},"ca_institutions":"Children's Hospital of Western Ontario","funders":"Eunice Kennedy Shriver National Institute of Child Health and Human Development; National Institute of General Medical Sciences","keywords":"Cornelia de Lange Syndrome; Cohesin; Genetics; Biology; Psychology; Gene; Meiosis","retraction":null,"screen_n_in":null,"score":{"opus":0.01325408091096749,"gpt":0.260067803820139,"spread":0.2468137229091715,"validation_status":"score_only:v0-immature-baseline"},"prediction":{"model_version":"codex-gemma-dda1882f352a","candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0003934014,0.00008948636,0.0001805861,0.00005795467,0.00004980763,0.00001095231,0.0001424632,0.00002357079,0.000005502433],"category_scores_gemma":[0.000008947198,0.00006662121,0.00003330296,0.00007984332,0.0002860237,0.000002179331,0.00003718255,0.00007802587,1.546865e-7],"about_ca_system_candidate":false,"about_ca_system_consensus":false,"about_ca_system_score_codex":0.00003024551,"about_ca_system_score_gemma":0.00005832413,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_topic_score_codex":0.00006865118,"about_ca_topic_score_gemma":0.0003788916,"domain_scores_codex":[0.9992979,0.00005901462,0.0003077238,0.00008729499,0.0001059382,0.0001421728],"domain_scores_gemma":[0.9992757,0.00001861297,0.0004340867,0.0001475425,0.0000687788,0.00005530848],"domain_codex":null,"domain_gemma":null,"domain_candidate":null,"domain_consensus":null,"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","study_design_scores_codex":[0.0005255201,0.0001861396,0.041779,0.00002922732,0.0002875937,0.0001342908,0.003143569,0.002677759,0.9493471,0.00008502534,0.0001334199,0.001671313],"study_design_scores_gemma":[0.002474667,0.006052295,0.9446594,0.0001033171,0.0002762872,0.004115789,0.005812747,0.00270998,0.03286606,0.0003382839,0.0002456884,0.0003455569],"study_design_candidate":"observational","study_design_consensus":null,"genre_codex":"empirical","genre_gemma":"empirical","genre_scores_codex":[0.9988144,0.0002120745,0.0007398257,0.00006349302,0.00001531995,0.00009931441,0.00001770996,9.343398e-7,0.00003690826],"genre_scores_gemma":[0.9946741,0.0001884019,0.005004088,0.00005894863,0.00002471166,9.203061e-7,0.00002046788,0.00001384587,0.00001451323],"genre_candidate":"empirical","genre_consensus":"empirical","teacher_disagreement_score":0.9164811,"threshold_uncertainty_score":0.2716734,"prediction_status":"machine_predicted_unvalidated"},"labels":[],"label_agreement":null},{"id":"W1974133253","doi":"10.1016/j.ajhg.2008.01.010","title":"Arrhythmogenic Right Ventricular Cardiomyopathy Type 5 Is a Fully Penetrant, Lethal Arrhythmic Disorder Caused by a Missense Mutation in the TMEM43 Gene","year":2008,"lang":"en","type":"article","venue":"The American Journal of Human Genetics","topic":"Cardiovascular Effects of Exercise","field":"Medicine","cited_by":509,"is_retracted":false,"has_abstract":false,"routes":{"ca_aff":true,"ca_fund":true,"ca_venue":false,"about_ca":false},"ca_institutions":"University of Toronto; Centre for Addiction and Mental Health; Memorial University of Newfoundland","funders":"Canadian Institutes of Health Research","keywords":"Penetrance; Missense mutation; Genetics; Cardiomyopathy; Haplotype; Biology; Population; Sudden death; Locus (genetics); Mendelian inheritance; Sudden cardiac death; Genetic heterogeneity; Internal medicine; Heart failure; Gene; Medicine; Mutation; Allele; Phenotype","retraction":null,"screen_n_in":null,"score":{"opus":0.00961178683728968,"gpt":0.2538600239151557,"spread":0.244248237077866,"validation_status":"score_only:v0-immature-baseline"},"prediction":{"model_version":"codex-gemma-dda1882f352a","candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.001068074,0.0002853194,0.0009453812,0.0002343085,0.0002030589,0.00002979906,0.000318824,0.00005344436,0.00003645776],"category_scores_gemma":[0.00008734898,0.0001713256,0.0007324494,0.0007163801,0.0004583415,0.00004389486,0.00003502153,0.0005367625,0.00001938213],"about_ca_system_candidate":false,"about_ca_system_consensus":false,"about_ca_system_score_codex":0.0001110397,"about_ca_system_score_gemma":0.0001988572,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_topic_score_codex":0.00007364935,"about_ca_topic_score_gemma":0.000007677871,"domain_scores_codex":[0.997171,0.0006122747,0.0006532068,0.0002357836,0.0009485354,0.0003791593],"domain_scores_gemma":[0.9981128,0.0001536903,0.0005578428,0.0007377286,0.0002982742,0.0001396962],"domain_codex":null,"domain_gemma":null,"domain_candidate":null,"domain_consensus":null,"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","study_design_scores_codex":[0.01048995,0.002761141,0.05528935,0.0003850394,0.01093844,0.3428494,0.04745103,0.01714777,0.4231023,0.00002466908,0.03575391,0.05380699],"study_design_scores_gemma":[0.02127945,0.01453372,0.4666692,0.0004728892,0.00681071,0.4308499,0.004324018,0.0008196986,0.03982282,0.0003567266,0.01244308,0.001617819],"study_design_candidate":"case_report","study_design_consensus":null,"genre_codex":"empirical","genre_gemma":"empirical","genre_scores_codex":[0.979277,0.01891407,0.0002787153,0.0007081156,0.0001290274,0.0006192217,0.0000076793,0.00001072393,0.00005541168],"genre_scores_gemma":[0.9968776,0.001592293,0.0002792251,0.0005658576,0.0005598239,0.00001073096,0.00001066599,0.00005283033,0.00005100868],"genre_candidate":"empirical","genre_consensus":"empirical","teacher_disagreement_score":0.4113798,"threshold_uncertainty_score":0.6986457,"prediction_status":"machine_predicted_unvalidated"},"labels":[],"label_agreement":null},{"id":"W4297900711","doi":"10.1016/j.ajhg.2009.09.012","title":"A Genome-wide Association Study of Lung Cancer Identifies a Region of Chromosome 5p15 Associated with Risk for Adenocarcinoma","year":2009,"lang":"en","type":"article","venue":"The American Journal of Human Genetics","topic":"Genetic Associations and Epidemiology","field":"Biochemistry, Genetics and Molecular Biology","cited_by":506,"is_retracted":false,"has_abstract":false,"routes":{"ca_aff":true,"ca_fund":false,"ca_venue":false,"about_ca":false},"ca_institutions":"Princess Margaret Cancer Centre; University Health Network; Lunenfeld-Tanenbaum Research Institute; University of Toronto","funders":"National Cancer Institute","keywords":"Lung cancer; Adenocarcinoma; Chromosome; Genome; Genome-wide association study; Cancer; Medicine; Oncology; Biology; Genetics; Internal medicine; Gene; Single-nucleotide polymorphism; Genotype","retraction":null,"screen_n_in":null,"score":{"opus":0.0143324845541667,"gpt":0.2862376567153517,"spread":0.271905172161185,"validation_status":"score_only:v0-immature-baseline"},"prediction":{"model_version":"codex-gemma-dda1882f352a","candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0008686171,0.0001441822,0.0005230429,0.00008216147,0.0001263101,0.000009861806,0.0003197438,0.0000639729,0.000002470789],"category_scores_gemma":[0.0004642022,0.0001048404,0.0001547631,0.0001830259,0.0001241307,0.000003765656,0.00003426007,0.0001306936,6.721688e-8],"about_ca_system_candidate":false,"about_ca_system_consensus":false,"about_ca_system_score_codex":0.00008531503,"about_ca_system_score_gemma":0.0001118108,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_topic_score_codex":0.00005541675,"about_ca_topic_score_gemma":0.0001441451,"domain_scores_codex":[0.9983042,0.0003943113,0.0006771298,0.0001569638,0.0002394682,0.0002279517],"domain_scores_gemma":[0.9951883,0.0001837858,0.003604623,0.0002664206,0.0007085945,0.0000482746],"domain_codex":null,"domain_gemma":null,"domain_candidate":null,"domain_consensus":null,"study_design_codex":"observational","study_design_gemma":"observational","study_design_scores_codex":[0.0001922475,0.0002813959,0.9702138,0.000006194053,0.0008589865,0.000001404897,0.001095857,0.002485909,0.02389585,0.000001225426,0.00053003,0.0004371039],"study_design_scores_gemma":[0.001133031,0.008404594,0.9861484,0.00002470561,0.0005661109,0.000004999621,0.001328384,0.00005930991,0.002021224,0.0001672061,0.00002596749,0.000116065],"study_design_candidate":"observational","study_design_consensus":"observational","genre_codex":"empirical","genre_gemma":"empirical","genre_scores_codex":[0.9972325,0.001451666,0.0006840059,0.000227583,0.00004627999,0.0003211277,0.00002303481,0.000002217728,0.00001157959],"genre_scores_gemma":[0.9988317,0.000558586,0.0002139732,0.0001049652,0.0001515445,0.000009830827,0.00001040318,0.00001724486,0.0001016747],"genre_candidate":"empirical","genre_consensus":"empirical","teacher_disagreement_score":0.02187462,"threshold_uncertainty_score":0.4275269,"prediction_status":"machine_predicted_unvalidated"},"labels":[],"label_agreement":null},{"id":"W1964955321","doi":"10.1016/j.ajhg.2011.05.003","title":"A Genome-wide Association Study of Lung Cancer Identifies a Region of Chromosome 5p15 Associated with Risk for Adenocarcinoma","year":2011,"lang":"en","type":"erratum","venue":"The American Journal of Human Genetics","topic":"Genetic Associations and Epidemiology","field":"Biochemistry, Genetics and Molecular Biology","cited_by":505,"is_retracted":false,"has_abstract":false,"routes":{"ca_aff":true,"ca_fund":false,"ca_venue":false,"about_ca":false},"ca_institutions":"University Health Network; University of Toronto","funders":"National Human Genome Research Institute","keywords":"Genome-wide association study; Lung cancer; Single-nucleotide polymorphism; Genotyping; Genetic association; Chromosome; Genetics; Human genome; Population; Oncology; Biology; Medicine; Genome; Bioinformatics; Gene; Genotype","retraction":null,"screen_n_in":null,"score":{"opus":0.01921718291336242,"gpt":0.2816286207934918,"spread":0.2624114378801294,"validation_status":"score_only:v0-immature-baseline"},"prediction":{"model_version":"codex-gemma-dda1882f352a","candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.001273895,0.0003288061,0.001213318,0.0001741814,0.0001743296,0.00001485693,0.0007093342,0.0002689169,0.00000837348],"category_scores_gemma":[0.000780173,0.0002431711,0.0003485348,0.0002253814,0.0002904276,0.000004018161,0.0001263653,0.000480053,1.654654e-7],"about_ca_system_candidate":false,"about_ca_system_consensus":false,"about_ca_system_score_codex":0.0001752671,"about_ca_system_score_gemma":0.0004338013,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_topic_score_codex":0.0002695884,"about_ca_topic_score_gemma":0.0007557224,"domain_scores_codex":[0.9969288,0.0007766993,0.001215171,0.0003028333,0.0004077638,0.0003687118],"domain_scores_gemma":[0.9874833,0.0002449332,0.01021614,0.000525286,0.001454966,0.00007538031],"domain_codex":null,"domain_gemma":null,"domain_candidate":null,"domain_consensus":null,"study_design_codex":"observational","study_design_gemma":"observational","study_design_scores_codex":[0.0003298124,0.0004637523,0.9275052,0.00006438098,0.005132631,0.00000429649,0.002181009,0.0005305565,0.002289471,7.137348e-7,0.06128886,0.0002092961],"study_design_scores_gemma":[0.001361553,0.01033711,0.9820151,0.0001429915,0.00266901,0.000008918318,0.001756107,0.00003009379,0.0003973971,0.0001260203,0.0008390975,0.0003166293],"study_design_candidate":"observational","study_design_consensus":"observational","genre_codex":"empirical","genre_gemma":"empirical","genre_scores_codex":[0.9921201,0.005953426,0.0003057831,0.00007202011,0.0007648186,0.0005778244,0.0001323814,0.000003018832,0.00007062142],"genre_scores_gemma":[0.991028,0.003842777,0.0001429265,0.00006297424,0.000726042,0.00004142935,0.0000996863,0.00007295109,0.003983239],"genre_candidate":"empirical","genre_consensus":"empirical","teacher_disagreement_score":0.06044977,"threshold_uncertainty_score":0.9916231,"prediction_status":"machine_predicted_unvalidated"},"labels":[],"label_agreement":null},{"id":"W2042581531","doi":"10.1086/303038","title":"mtDNA Variation among Greenland Eskimos: The Edge of the Beringian Expansion","year":2000,"lang":"en","type":"article","venue":"The American Journal of Human Genetics","topic":"Indigenous Studies and Ecology","field":"Health Professions","cited_by":502,"is_retracted":false,"has_abstract":false,"routes":{"ca_aff":true,"ca_fund":false,"ca_venue":false,"about_ca":false},"ca_institutions":"Arthur B. McDonald-Canadian Astroparticle Physics Research Institute","funders":"","keywords":"Mitochondrial DNA; Hypervariable region; mtDNA control region; Geography; Evolutionary biology; Biology; Archaeology; Genealogy; History; Genetics; Haplotype; Gene","retraction":null,"screen_n_in":null,"score":{"opus":0.0217706801815994,"gpt":0.3277201066966461,"spread":0.3059494265150467,"validation_status":"score_only:v0-immature-baseline"},"prediction":{"model_version":"codex-gemma-dda1882f352a","candidate_categories":["sts"],"consensus_categories":[],"category_scores_codex":[0.001084989,0.0001060173,0.0002902235,0.00003243976,0.002826452,0.000005924257,0.0005385491,0.00003896539,0.0003308161],"category_scores_gemma":[0.00003427086,0.0000472242,0.000114979,0.0001776859,0.0004638933,0.00002273441,0.0001232181,0.0005126767,0.00001583516],"about_ca_system_candidate":false,"about_ca_system_consensus":false,"about_ca_system_score_codex":0.00007955902,"about_ca_system_score_gemma":0.0001492599,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_topic_score_codex":0.0009145536,"about_ca_topic_score_gemma":0.002119119,"domain_scores_codex":[0.9980245,0.0006857951,0.0005933885,0.00007632808,0.0002252562,0.0003947253],"domain_scores_gemma":[0.9980465,0.0002634164,0.001059755,0.0003729547,0.0002149504,0.00004241444],"domain_codex":null,"domain_gemma":null,"domain_candidate":null,"domain_consensus":null,"study_design_codex":"qualitative","study_design_gemma":"observational","study_design_scores_codex":[0.0003932021,0.0002492562,0.4234543,0.00007544689,0.000598833,0.00001031378,0.5025303,0.002917237,0.003835302,0.0004634282,0.007105335,0.05836702],"study_design_scores_gemma":[0.0003515818,0.000750072,0.9721367,0.00006025877,0.0001184104,0.00001423568,0.02199396,0.00007273992,0.00005991544,0.0006345733,0.003728349,0.00007921619],"study_design_candidate":"observational","study_design_consensus":null,"genre_codex":"empirical","genre_gemma":"empirical","genre_scores_codex":[0.9954499,0.000255048,0.00005687557,0.001466887,0.0003332526,0.0003021888,0.000003620357,0.000004204864,0.002128021],"genre_scores_gemma":[0.9976289,0.0004598847,0.00009603363,0.0007051008,0.0005249409,0.000005761861,3.724182e-7,0.00001683721,0.00056222],"genre_candidate":"empirical","genre_consensus":"empirical","teacher_disagreement_score":0.5486823,"threshold_uncertainty_score":0.9984717,"prediction_status":"machine_predicted_unvalidated"},"labels":[],"label_agreement":null},{"id":"W2044994496","doi":"10.1086/302913","title":"Genomewide Search in Canadian Families with Inflammatory Bowel Disease Reveals Two Novel Susceptibility Loci","year":2000,"lang":"en","type":"article","venue":"The American Journal of Human Genetics","topic":"Inflammatory Bowel Disease","field":"Biochemistry, Genetics and Molecular Biology","cited_by":500,"is_retracted":false,"has_abstract":false,"routes":{"ca_aff":true,"ca_fund":true,"ca_venue":false,"about_ca":true},"ca_institutions":"Queen Elizabeth II Health Sciences Centre; McGill University; University of Toronto; SickKids Foundation; Dalhousie University; Hospital for Sick Children","funders":"Hospital for Sick Children; University of Toronto; Physicians' Services Incorporated Foundation","keywords":"Inflammatory bowel disease; Locus (genetics); Ulcerative colitis; Etiology; Genetics; Disease; Crohn's disease; Genetic linkage; Biology; Epidemiology; Genetic predisposition; Immunology; Medicine; Gene; Internal medicine","retraction":null,"screen_n_in":null,"score":{"opus":0.008325737510568686,"gpt":0.2544244172361034,"spread":0.2460986797255347,"validation_status":"score_only:v0-immature-baseline"},"prediction":{"model_version":"codex-gemma-dda1882f352a","candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0007526626,0.0002303464,0.0002454152,0.0001505105,0.0001740046,0.00004396601,0.0006298839,0.0000341909,0.00008966012],"category_scores_gemma":[0.00002844127,0.0001749658,0.000122334,0.0001532553,0.0008417579,0.00000852723,0.00005506674,0.0002735216,0.00001188336],"about_ca_system_candidate":false,"about_ca_system_consensus":false,"about_ca_system_score_codex":0.000139658,"about_ca_system_score_gemma":0.001085727,"about_ca_topic_candidate":true,"about_ca_topic_consensus":false,"about_ca_topic_score_codex":0.00277742,"about_ca_topic_score_gemma":0.04832531,"domain_scores_codex":[0.998098,0.0002567454,0.0005006702,0.0002555026,0.0003308069,0.0005582806],"domain_scores_gemma":[0.9981984,0.00001732096,0.0002457023,0.0006746251,0.0002146594,0.0006492923],"domain_codex":null,"domain_gemma":null,"domain_candidate":null,"domain_consensus":null,"study_design_codex":"observational","study_design_gemma":"observational","study_design_scores_codex":[0.00136642,0.0001218121,0.9254502,0.0000385799,0.0001229533,0.0004458546,0.000645224,0.01898867,0.04915182,0.0000351432,0.0002200541,0.003413253],"study_design_scores_gemma":[0.0008902454,0.0004960832,0.9956937,0.00003486565,0.00005169177,0.00004631353,0.0005565268,0.00007511822,0.000598903,0.00007774639,0.001213399,0.0002654436],"study_design_candidate":"observational","study_design_consensus":"observational","genre_codex":"empirical","genre_gemma":"empirical","genre_scores_codex":[0.9988694,0.0003710812,0.00002209961,0.0001380651,0.00002217698,0.0002237503,0.00004100324,0.000004102265,0.0003083897],"genre_scores_gemma":[0.9983735,0.0002357308,0.0002780757,0.0005679017,0.0002797752,0.000005684549,0.00001819778,0.00004270111,0.0001984182],"genre_candidate":"empirical","genre_consensus":"empirical","teacher_disagreement_score":0.07024345,"threshold_uncertainty_score":0.9690403,"prediction_status":"machine_predicted_unvalidated"},"labels":[],"label_agreement":null},{"id":"W2040026415","doi":"10.1016/j.ajhg.2013.06.012","title":"Detection of Clinically Relevant Genetic Variants in Autism Spectrum Disorder by Whole-Genome Sequencing","year":2013,"lang":"en","type":"article","venue":"The American Journal of Human Genetics","topic":"Autism Spectrum Disorder Research","field":"Neuroscience","cited_by":497,"is_retracted":false,"has_abstract":false,"routes":{"ca_aff":true,"ca_fund":true,"ca_venue":false,"about_ca":false},"ca_institutions":"University of Alberta; Holland Bloorview Kids Rehabilitation Hospital; University of Toronto; SickKids Foundation; McMaster University; Hospital for Sick Children","funders":"National Institute of Mental Health; Canadian Institutes of Health Research; National Key Research and Development Program of China; National Institutes of Health; European Bioinformatics Institute; Eunice Kennedy Shriver National Institute of Child Health and Human Development; Autism Speaks","keywords":"Genetics; Autism spectrum disorder; Missense mutation; Autism; Proband; Biology; Gene; Heritability of autism; Loss function; Genetic heterogeneity; Copy-number variation; Genome; Mutation; Phenotype; Medicine; Psychiatry","retraction":null,"screen_n_in":null,"score":{"opus":0.02520357549978174,"gpt":0.2989347829920581,"spread":0.2737312074922764,"validation_status":"score_only:v0-immature-baseline"},"prediction":{"model_version":"codex-gemma-dda1882f352a","candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0007379155,0.0002062133,0.0005007465,0.000284185,0.0001642804,0.0000691412,0.001054313,0.00004508844,0.0001099515],"category_scores_gemma":[0.0002084879,0.0001565458,0.0001356375,0.0007122064,0.0008913028,0.0001171035,0.000185841,0.0007025439,0.00004968314],"about_ca_system_candidate":false,"about_ca_system_consensus":false,"about_ca_system_score_codex":0.0001528362,"about_ca_system_score_gemma":0.0001658046,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_topic_score_codex":0.000358468,"about_ca_topic_score_gemma":0.00006607267,"domain_scores_codex":[0.9964333,0.0006942637,0.00131647,0.0002989165,0.0007083367,0.000548748],"domain_scores_gemma":[0.9976155,0.0003157867,0.001366651,0.0005208885,0.0000306631,0.0001504987],"domain_codex":null,"domain_gemma":null,"domain_candidate":null,"domain_consensus":null,"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","study_design_scores_codex":[0.00005022863,0.0001221014,0.003752436,0.000008257151,0.00001508752,0.00002358495,0.0007790956,0.001028927,0.9881958,0.0001288323,0.00001211531,0.005883478],"study_design_scores_gemma":[0.00299332,0.01412066,0.7621759,0.000157154,0.0001080957,0.001022893,0.001866034,0.007042633,0.1219221,0.08707686,0.0005491312,0.0009652768],"study_design_candidate":"bench_or_experimental","study_design_consensus":null,"genre_codex":"empirical","genre_gemma":"empirical","genre_scores_codex":[0.9935844,0.0004243333,0.002505638,0.002948096,0.00008510566,0.0003234279,0.000008947814,0.00001142617,0.0001086355],"genre_scores_gemma":[0.9983457,0.0007835458,0.0004817291,0.0001891026,0.00005461079,0.000006926427,4.214579e-7,0.00004698397,0.00009094015],"genre_candidate":"empirical","genre_consensus":"empirical","teacher_disagreement_score":0.8662738,"threshold_uncertainty_score":0.6383754,"prediction_status":"machine_predicted_unvalidated"},"labels":[],"label_agreement":null},{"id":"W2079813075","doi":"10.1086/499409","title":"SLC34A3 Mutations in Patients with Hereditary Hypophosphatemic Rickets with Hypercalciuria Predict a Key Role for the Sodium-Phosphate Cotransporter NaPi-IIc in Maintaining Phosphate Homeostasis","year":2006,"lang":"en","type":"article","venue":"The American Journal of Human Genetics","topic":"Parathyroid Disorders and Treatments","field":"Medicine","cited_by":488,"is_retracted":false,"has_abstract":false,"routes":{"ca_aff":true,"ca_fund":true,"ca_venue":false,"about_ca":false},"ca_institutions":"McGill University; Simon Fraser University; McGill University Health Centre","funders":"Eunice Kennedy Shriver National Institute of Child Health and Human Development; National Institute of Diabetes and Digestive and Kidney Diseases; Canadian Institutes of Health Research; National Institutes of Health","keywords":"Hypercalciuria; Hypophosphatemic Rickets; Phosphate; Cotransporter; Hypophosphatemia; Endocrinology; Rickets; Internal medicine; Sodium; Homeostasis; Medicine; Chemistry; Biochemistry; Vitamin D and neurology; Calcium","retraction":null,"screen_n_in":null,"score":{"opus":0.0077922035799914,"gpt":0.2389319664143695,"spread":0.231139762834378,"validation_status":"score_only:v0-immature-baseline"},"prediction":{"model_version":"codex-gemma-dda1882f352a","candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0002731404,0.0002807281,0.0005659592,0.0001655288,0.0001862634,0.00003139108,0.0002517477,0.00003330666,0.000009329938],"category_scores_gemma":[0.000008636376,0.0001490155,0.0001121149,0.0004568232,0.0004330652,0.00008695633,0.00001732063,0.0002931924,0.00000237606],"about_ca_system_candidate":false,"about_ca_system_consensus":false,"about_ca_system_score_codex":0.0001261378,"about_ca_system_score_gemma":0.0001735322,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_topic_score_codex":0.000332827,"about_ca_topic_score_gemma":0.000309501,"domain_scores_codex":[0.9981843,0.00006951579,0.0006345712,0.0002167332,0.0004511445,0.000443713],"domain_scores_gemma":[0.9986648,0.0001429204,0.0005878165,0.0003003463,0.0001996208,0.000104506],"domain_codex":null,"domain_gemma":null,"domain_candidate":null,"domain_consensus":null,"study_design_codex":"observational","study_design_gemma":"observational","study_design_scores_codex":[0.004758325,0.0009221951,0.9796761,0.00000965351,0.0003946583,0.0001975205,0.001887908,0.006564627,0.00008372711,0.00002523136,0.0002244612,0.005255537],"study_design_scores_gemma":[0.01223867,0.005716131,0.9770784,0.0001160827,0.0005659143,0.00008318655,0.002432952,0.0004021681,0.0004446903,0.0006108782,0.0001128234,0.0001980516],"study_design_candidate":"observational","study_design_consensus":"observational","genre_codex":"empirical","genre_gemma":"empirical","genre_scores_codex":[0.9895535,0.008804259,0.0003375234,0.0003317463,0.00004902463,0.0008203516,0.000039658,0.00001012248,0.00005384739],"genre_scores_gemma":[0.997856,0.0002819098,0.001354515,0.0002523784,0.00007742443,0.0000490392,0.0000453734,0.00005557807,0.00002777291],"genre_candidate":"empirical","genre_consensus":"empirical","teacher_disagreement_score":0.008522348,"threshold_uncertainty_score":0.6076677,"prediction_status":"machine_predicted_unvalidated"},"labels":[],"label_agreement":null},{"id":"W2766662494","doi":"10.1016/j.ajhg.2017.09.008","title":"High Rate of Recurrent De Novo Mutations in Developmental and Epileptic Encephalopathies","year":2017,"lang":"en","type":"review","venue":"The American Journal of Human Genetics","topic":"Genomics and Rare Diseases","field":"Biochemistry, Genetics and Molecular Biology","cited_by":456,"is_retracted":false,"has_abstract":false,"routes":{"ca_aff":true,"ca_fund":true,"ca_venue":false,"about_ca":false},"ca_institutions":"Centre hospitalier universitaire de Québec; Cégep de l'Abitibi Témiscamingue; Children's Hospital of Eastern Ontario; Centre Hospitalier Universitaire de Sherbrooke; University of British Columbia; Toronto Western Hospital; Université du Québec à Chicoutimi; Université de Montréal; Hospital for Sick Children; Université du Québec à Montréal; McGill University and Génome Québec Innovation Centre; Montreal Neurological Institute and Hospital; McGill Genome Centre; SickKids Foundation; Université de Sherbrooke; University of Toronto; McGill University; BC Children's Hospital; Centre Hospitalier de l’Université de Montréal; Centre Hospitalier Universitaire Sainte-Justine","funders":"Eunice Kennedy Shriver National Institute of Child Health and Human Development; National Human Genome Research Institute; University of Toronto; Génome Québec; Fondation Jean-Louis Lévesque; National Institute of Neurological Disorders and Stroke; National Institute of General Medical Sciences; Ontario Brain Institute; Genome Canada","keywords":"Genetics; Missense mutation; Candidate gene; Biology; Gene; Intellectual disability; Epilepsy; Whole genome sequencing; Mutation; Genome; Neuroscience","retraction":null,"screen_n_in":null,"score":{"opus":0.04638554223442326,"gpt":0.3383900866201144,"spread":0.2920045443856912,"validation_status":"score_only:v0-immature-baseline"},"prediction":{"model_version":"codex-gemma-dda1882f352a","candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0003539727,0.0001744797,0.0006559844,0.0001018514,0.00009363008,0.00002603981,0.0004166853,0.00004471107,0.000003641568],"category_scores_gemma":[0.00006258585,0.0001206713,0.0001676945,0.000052683,0.000495162,0.00000169405,0.0001214393,0.0001527225,6.072679e-7],"about_ca_system_candidate":false,"about_ca_system_consensus":false,"about_ca_system_score_codex":0.00002815953,"about_ca_system_score_gemma":0.0004852936,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_topic_score_codex":0.000009670257,"about_ca_topic_score_gemma":0.00001761033,"domain_scores_codex":[0.9989176,0.0001946628,0.0005390288,0.0001262012,0.00007354656,0.0001489865],"domain_scores_gemma":[0.998359,0.00003314788,0.001250264,0.0002051468,0.00008397767,0.00006848652],"domain_codex":null,"domain_gemma":null,"domain_candidate":null,"domain_consensus":null,"study_design_codex":"design_other","study_design_gemma":"not_applicable","study_design_scores_codex":[0.00003963427,0.00009206416,0.0003393028,0.0006251198,0.0002719709,0.0000560007,0.0003405414,0.00002832453,0.001612858,0.00002699122,0.00006217796,0.996505],"study_design_scores_gemma":[0.003447521,0.01256819,0.03705529,0.01914487,0.005688461,0.008277068,0.004868691,0.0000115843,0.003148321,0.00373846,0.8989504,0.003101165],"study_design_candidate":"design_other","study_design_consensus":null,"genre_codex":"review","genre_gemma":"review","genre_scores_codex":[0.4111073,0.5887154,0.00001059301,0.000007644301,0.00004478408,0.00007712285,0.00002599754,3.634992e-7,0.0000107157],"genre_scores_gemma":[0.1693319,0.8297509,0.00073215,0.00001637702,0.0001091143,0.000004380719,0.00002081026,0.00001756904,0.00001680227],"genre_candidate":"review","genre_consensus":"review","teacher_disagreement_score":0.9934039,"threshold_uncertainty_score":0.4920833,"prediction_status":"machine_predicted_unvalidated"},"labels":[],"label_agreement":null},{"id":"W1742756123","doi":"10.1016/j.ajhg.2014.08.013","title":"De Novo Mutations in Synaptic Transmission Genes Including DNM1 Cause Epileptic Encephalopathies","year":2014,"lang":"en","type":"article","venue":"The American Journal of Human Genetics","topic":"Genetics and Neurodevelopmental Disorders","field":"Biochemistry, Genetics and Molecular Biology","cited_by":454,"is_retracted":false,"has_abstract":false,"routes":{"ca_aff":false,"ca_fund":true,"ca_venue":false,"about_ca":false},"ca_institutions":"","funders":"Institute of Genetics; National Institute of Neurological Disorders and Stroke","keywords":"Gene; Neurotransmission; Neuroscience; Epilepsy; Biology; Mutation; Genetics","retraction":null,"screen_n_in":null,"score":{"opus":0.01652736485360838,"gpt":0.276299430569979,"spread":0.2597720657163706,"validation_status":"score_only:v0-immature-baseline"},"prediction":{"model_version":"codex-gemma-dda1882f352a","candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0004032846,0.00014454,0.0002015218,0.0001066104,0.0001479538,0.00002976341,0.000355244,0.00003391839,0.00000871564],"category_scores_gemma":[0.00004173279,0.0001135756,0.00008444495,0.0001568431,0.0002960224,0.000003178299,0.00006811997,0.0001489984,0.000001871807],"about_ca_system_candidate":false,"about_ca_system_consensus":false,"about_ca_system_score_codex":0.00002153055,"about_ca_system_score_gemma":0.00009161171,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_topic_score_codex":0.000007579991,"about_ca_topic_score_gemma":0.0000232676,"domain_scores_codex":[0.998841,0.0002074224,0.0003848543,0.0001485672,0.0001688256,0.0002492639],"domain_scores_gemma":[0.9993185,0.0000363041,0.0002823104,0.0001952271,0.00007578798,0.00009189965],"domain_codex":null,"domain_gemma":null,"domain_candidate":null,"domain_consensus":null,"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","study_design_scores_codex":[0.00004714448,0.00006495729,0.01121255,0.000009387375,0.000051493,0.00001052697,0.000830757,0.004545774,0.9507092,0.00002494375,0.00003006378,0.03246317],"study_design_scores_gemma":[0.002819705,0.008586528,0.6155608,0.0002267223,0.000325502,0.001200668,0.005057109,0.002086833,0.3511229,0.004434707,0.007427248,0.001151219],"study_design_candidate":"bench_or_experimental","study_design_consensus":null,"genre_codex":"empirical","genre_gemma":"empirical","genre_scores_codex":[0.9947369,0.001121862,0.003710376,0.0002060443,0.00005124946,0.00007228843,0.000001370035,0.000002851508,0.00009704242],"genre_scores_gemma":[0.9955957,0.001345471,0.002614684,0.0003256449,0.00005953681,0.000003696548,0.000004011058,0.00002488391,0.00002635791],"genre_candidate":"empirical","genre_consensus":"empirical","teacher_disagreement_score":0.6043483,"threshold_uncertainty_score":0.4631477,"prediction_status":"machine_predicted_unvalidated"},"labels":[],"label_agreement":null},{"id":"W2611574484","doi":"10.1016/j.ajhg.2017.04.003","title":"International Cooperation to Enable the Diagnosis of All Rare Genetic Diseases","year":2017,"lang":"en","type":"article","venue":"The American Journal of Human Genetics","topic":"Genomics and Rare Diseases","field":"Biochemistry, Genetics and Molecular Biology","cited_by":453,"is_retracted":false,"has_abstract":true,"routes":{"ca_aff":true,"ca_fund":true,"ca_venue":false,"about_ca":false},"ca_institutions":"Canada's Michael Smith Genome Sciences Centre; University of Toronto; University of British Columbia; McGill University; Children's Hospital of Eastern Ontario; University of Ottawa","funders":"National Human Genome Research Institute; National Heart, Lung, and Blood Institute; Medical Research Council; Ontario Genomics Institute; Canadian Institutes of Health Research; Genome Canada; Ontario Genomics; Wellcome Trust; European Commission; Johns Hopkins University; University of Washington","keywords":"Computer science; Computational biology; Biology","retraction":null,"screen_n_in":null,"score":{"opus":0.01485170619201797,"gpt":0.2918985219165635,"spread":0.2770468157245455,"validation_status":"score_only:v0-immature-baseline"},"prediction":{"model_version":"codex-gemma-dda1882f352a","candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0001183041,0.00009550394,0.0001456002,0.00003066227,0.0002433138,0.00008674577,0.0009978171,0.00001535854,0.00002531931],"category_scores_gemma":[0.00009995536,0.00005694702,0.0001230406,0.000025374,0.0002946436,0.000003579207,0.000201674,0.00005447173,0.000002094228],"about_ca_system_candidate":false,"about_ca_system_consensus":false,"about_ca_system_score_codex":0.000009624018,"about_ca_system_score_gemma":0.00006590601,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_topic_score_codex":0.0000222519,"about_ca_topic_score_gemma":0.00001504657,"domain_scores_codex":[0.9992863,0.00006268889,0.0002620429,0.0001038103,0.0001649277,0.000120222],"domain_scores_gemma":[0.9985674,0.00001780436,0.0005581819,0.0005065984,0.0002642493,0.00008577745],"domain_codex":null,"domain_gemma":null,"domain_candidate":null,"domain_consensus":null,"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","study_design_scores_codex":[0.0008528997,0.0006418841,0.2212225,0.00002721056,0.001468214,0.00006325717,0.001382768,0.01564492,0.6392498,0.0002165933,0.03719643,0.08203349],"study_design_scores_gemma":[0.001246771,0.004655523,0.694944,0.00007427717,0.0005600666,0.0001891935,0.001372457,0.0001439154,0.1651275,0.0007141271,0.1304672,0.0005050066],"study_design_candidate":"observational","study_design_consensus":null,"genre_codex":"empirical","genre_gemma":"empirical","genre_scores_codex":[0.9971203,0.00106087,0.0001521391,0.001215597,0.0001688496,0.00009750482,0.00004257943,9.768888e-7,0.0001412427],"genre_scores_gemma":[0.9971156,0.001380533,0.0003098216,0.0005521675,0.000525372,0.000007046152,0.000009275639,0.00001433825,0.00008584747],"genre_candidate":"empirical","genre_consensus":"empirical","teacher_disagreement_score":0.4741223,"threshold_uncertainty_score":0.2322232,"prediction_status":"machine_predicted_unvalidated"},"labels":[],"label_agreement":null},{"id":"W2066250513","doi":"10.1086/375614","title":"Mutations in the Transcription Factor Gene SOX18 Underlie Recessive and Dominant Forms of Hypotrichosis-Lymphedema-Telangiectasia","year":2003,"lang":"en","type":"article","venue":"The American Journal of Human Genetics","topic":"Lymphatic System and Diseases","field":"Medicine","cited_by":428,"is_retracted":false,"has_abstract":false,"routes":{"ca_aff":true,"ca_fund":false,"ca_venue":false,"about_ca":false},"ca_institutions":"University of Toronto","funders":"","keywords":"Biology; Genetics; Missense mutation; Germline mutation; Hypotrichosis; Gene; Cancer research; Mutation","retraction":null,"screen_n_in":null,"score":{"opus":0.02897352887290012,"gpt":0.3009538484075227,"spread":0.2719803195346226,"validation_status":"score_only:v0-immature-baseline"},"prediction":{"model_version":"codex-gemma-dda1882f352a","candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0003356533,0.0001065356,0.0003411554,0.000124168,0.00008465462,0.00001731857,0.0001344246,0.00001934125,0.00001673967],"category_scores_gemma":[0.00007945953,0.00005302508,0.0001054034,0.0002452017,0.0002959845,0.00003757959,0.000005924639,0.00002938692,8.090379e-7],"about_ca_system_candidate":false,"about_ca_system_consensus":false,"about_ca_system_score_codex":0.00004728275,"about_ca_system_score_gemma":0.0001421367,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_topic_score_codex":0.00001627736,"about_ca_topic_score_gemma":0.000008386251,"domain_scores_codex":[0.998782,0.0002209707,0.000477643,0.00007787903,0.0003014406,0.0001400522],"domain_scores_gemma":[0.9988958,0.0001860719,0.0005444172,0.0001828323,0.000115915,0.00007502268],"domain_codex":null,"domain_gemma":null,"domain_candidate":null,"domain_consensus":null,"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","study_design_scores_codex":[0.001352241,0.001994141,0.3035434,0.0004261194,0.001126186,0.0003148609,0.0645433,0.0003918185,0.5609992,0.002542571,0.0007392659,0.06202691],"study_design_scores_gemma":[0.006104797,0.004843415,0.8827468,0.0003567373,0.001325286,0.002646,0.05813718,0.00007375239,0.0375799,0.00568454,0.0002182365,0.0002834074],"study_design_candidate":"observational","study_design_consensus":null,"genre_codex":"empirical","genre_gemma":"empirical","genre_scores_codex":[0.9954574,0.003233542,0.0004515788,0.0002410393,0.00004307951,0.0002132811,0.000006652322,0.00000210783,0.0003513437],"genre_scores_gemma":[0.9988243,0.0004943755,0.0003985152,0.0001935304,0.00005376899,0.000004524705,0.000001785364,0.00001151718,0.00001770114],"genre_candidate":"empirical","genre_consensus":"empirical","teacher_disagreement_score":0.5792034,"threshold_uncertainty_score":0.21623,"prediction_status":"machine_predicted_unvalidated"},"labels":[],"label_agreement":null},{"id":"W1979250362","doi":"10.1086/512864","title":"Characterization of Potocki-Lupski Syndrome (dup(17)(p11.2p11.2)) and Delineation of a Dosage-Sensitive Critical Interval That Can Convey an Autism Phenotype","year":2007,"lang":"en","type":"article","venue":"The American Journal of Human Genetics","topic":"Genomic variations and chromosomal abnormalities","field":"Biochemistry, Genetics and Molecular Biology","cited_by":428,"is_retracted":false,"has_abstract":false,"routes":{"ca_aff":true,"ca_fund":false,"ca_venue":false,"about_ca":false},"ca_institutions":"University of Toronto","funders":"Eunice Kennedy Shriver National Institute of Child Health and Human Development; National Center for Research Resources; National Institute of Child Health and Human Development; National Institutes of Health; Deutsches Krebsforschungszentrum; Research to Prevent Blindness","keywords":"dup; Autism; Phenotype; Interval (graph theory); Characterization (materials science); Genetics; Biology; Physics; Gene duplication; Psychology; Mathematics; Combinatorics; Developmental psychology; Gene; Optics","retraction":null,"screen_n_in":null,"score":{"opus":0.01310835826325019,"gpt":0.2672927106487838,"spread":0.2541843523855337,"validation_status":"score_only:v0-immature-baseline"},"prediction":{"model_version":"codex-gemma-dda1882f352a","candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0004317528,0.0001237642,0.0002793553,0.00007697679,0.00007654667,0.00001640461,0.0001681102,0.00004745313,0.00001325327],"category_scores_gemma":[0.00003080081,0.0001005075,0.00007185643,0.00007416277,0.0004282525,0.000009298003,0.00006478783,0.0000987285,2.229734e-7],"about_ca_system_candidate":false,"about_ca_system_consensus":false,"about_ca_system_score_codex":0.00001579715,"about_ca_system_score_gemma":0.00006773876,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_topic_score_codex":0.00004692234,"about_ca_topic_score_gemma":0.00003452464,"domain_scores_codex":[0.9989398,0.0001290577,0.0004875139,0.0001187339,0.0001652216,0.0001596332],"domain_scores_gemma":[0.9987828,0.00003339553,0.0006242075,0.0001945152,0.0002915018,0.00007354825],"domain_codex":null,"domain_gemma":null,"domain_candidate":null,"domain_consensus":null,"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","study_design_scores_codex":[0.0001850767,0.00009671566,0.01604879,0.00002218249,0.0001227219,0.00001030753,0.0016368,0.00005701128,0.9784541,0.0003211771,0.000009657491,0.003035514],"study_design_scores_gemma":[0.0005804339,0.004837156,0.4218367,0.00006227782,0.0001742948,0.0005550638,0.002915502,0.0001037981,0.5683761,0.0002180855,0.0001301655,0.0002104215],"study_design_candidate":"bench_or_experimental","study_design_consensus":"bench_or_experimental","genre_codex":"empirical","genre_gemma":"empirical","genre_scores_codex":[0.9878972,0.00009821271,0.01159845,0.0001660446,0.0000679759,0.00009460274,0.00005001909,0.000002158602,0.00002531768],"genre_scores_gemma":[0.9986032,0.0001000424,0.0009224378,0.0001602718,0.0001075691,9.135404e-7,0.00004054365,0.0000167765,0.00004822308],"genre_candidate":"empirical","genre_consensus":"empirical","teacher_disagreement_score":0.410078,"threshold_uncertainty_score":0.4098576,"prediction_status":"machine_predicted_unvalidated"},"labels":[],"label_agreement":null},{"id":"W2752403657","doi":"10.1016/j.ajhg.2017.07.014","title":"Variant Interpretation: Functional Assays to the Rescue","year":2017,"lang":"en","type":"article","venue":"The American Journal of Human Genetics","topic":"CRISPR and Genetic Engineering","field":"Biochemistry, Genetics and Molecular Biology","cited_by":427,"is_retracted":false,"has_abstract":false,"routes":{"ca_aff":true,"ca_fund":true,"ca_venue":false,"about_ca":false},"ca_institutions":"Lunenfeld-Tanenbaum Research Institute; University of Toronto; Ontario Institute for Cancer Research; Canadian Institute for Advanced Research","funders":"National Human Genome Research Institute; National Institute of General Medical Sciences; Canadian Institute for Advanced Research; Canada Excellence Research Chairs, Government of Canada; Division of Cancer Prevention, National Cancer Institute; Howard Hughes Medical Institute; National Cancer Institute; National Institutes of Health; National Science Foundation","keywords":"Interpretation (philosophy); Computational biology; Biology; Computer science; Programming language","retraction":null,"screen_n_in":null,"score":{"opus":0.01304228263719491,"gpt":0.3165963790144947,"spread":0.3035540963772998,"validation_status":"score_only:v0-immature-baseline"},"prediction":{"model_version":"codex-gemma-dda1882f352a","candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0004285921,0.00009689329,0.0001251403,0.00002704159,0.0003650915,0.00008903725,0.0006996072,0.0000187052,0.00001452693],"category_scores_gemma":[0.00009053888,0.00005749578,0.0001012127,0.00003386465,0.0001884572,0.000002431562,0.0001593818,0.0001317216,0.000006712747],"about_ca_system_candidate":false,"about_ca_system_consensus":false,"about_ca_system_score_codex":0.000009478395,"about_ca_system_score_gemma":0.00004494228,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_topic_score_codex":0.000009477441,"about_ca_topic_score_gemma":0.00003684898,"domain_scores_codex":[0.9992961,0.00005931277,0.0002232339,0.0001023719,0.0001784523,0.0001405697],"domain_scores_gemma":[0.998917,0.00001585219,0.0002523409,0.0006023881,0.0001414085,0.0000709959],"domain_codex":null,"domain_gemma":null,"domain_candidate":null,"domain_consensus":null,"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","study_design_scores_codex":[0.0006757826,0.00009995508,0.003555685,0.00001203773,0.0006507973,0.00003631401,0.001870548,0.1126446,0.7405346,0.000387399,0.03170503,0.1078273],"study_design_scores_gemma":[0.0017558,0.009024773,0.6371942,0.0001266841,0.0004390389,0.001869542,0.002870414,0.002935313,0.1787002,0.001076253,0.1630296,0.0009781906],"study_design_candidate":"bench_or_experimental","study_design_consensus":null,"genre_codex":"empirical","genre_gemma":"empirical","genre_scores_codex":[0.9420319,0.0004935354,0.05447843,0.002099225,0.0003754168,0.00007491686,0.000003722573,0.000002180719,0.0004406989],"genre_scores_gemma":[0.9971238,0.00009151803,0.0009704462,0.000508816,0.001038699,0.000002738623,0.000001465521,0.00001507468,0.0002474037],"genre_candidate":"empirical","genre_consensus":"empirical","teacher_disagreement_score":0.6336386,"threshold_uncertainty_score":0.2808026,"prediction_status":"machine_predicted_unvalidated"},"labels":[],"label_agreement":null},{"id":"W2000064832","doi":"10.1086/367713","title":"Expansion of the Fragile X CGG Repeat in Females with Premutation or Intermediate Alleles","year":2003,"lang":"en","type":"article","venue":"The American Journal of Human Genetics","topic":"Genetics and Neurodevelopmental Disorders","field":"Biochemistry, Genetics and Molecular Biology","cited_by":421,"is_retracted":false,"has_abstract":false,"routes":{"ca_aff":true,"ca_fund":false,"ca_venue":false,"about_ca":false},"ca_institutions":"Université Laval","funders":"Eunice Kennedy Shriver National Institute of Child Health and Human Development; Helsingin ja Uudenmaan Sairaanhoitopiiri","keywords":"Allele; Fragile x; Fragile X syndrome; Genetics; Biology; Trinucleotide repeat expansion; Gene","retraction":null,"screen_n_in":null,"score":{"opus":0.01337963947049709,"gpt":0.256072354724645,"spread":0.2426927152541479,"validation_status":"score_only:v0-immature-baseline"},"prediction":{"model_version":"codex-gemma-dda1882f352a","candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0001813584,0.0001033066,0.0001543249,0.0000393369,0.00005568871,0.000009377414,0.0002730523,0.00001997616,0.000007390128],"category_scores_gemma":[0.00003917253,0.00005302915,0.00005697495,0.0001254372,0.0003050382,0.00000201146,0.00005137741,0.00009522434,3.016168e-7],"about_ca_system_candidate":false,"about_ca_system_consensus":false,"about_ca_system_score_codex":0.000008646107,"about_ca_system_score_gemma":0.0001135689,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_topic_score_codex":0.000004087198,"about_ca_topic_score_gemma":0.00008454316,"domain_scores_codex":[0.9991298,0.0001612296,0.000304638,0.000106632,0.0001733913,0.0001243585],"domain_scores_gemma":[0.9991974,0.0000152595,0.0004445172,0.0002268893,0.00008489532,0.0000310989],"domain_codex":null,"domain_gemma":null,"domain_candidate":null,"domain_consensus":null,"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","study_design_scores_codex":[0.0003609098,0.00009917729,0.06222306,0.00001496658,0.00006854309,0.000006555201,0.001239318,0.002723809,0.9284968,0.0000221134,0.0001507938,0.004593916],"study_design_scores_gemma":[0.0008300599,0.003148772,0.4975113,0.00007518401,0.00003901671,0.0001161374,0.003016433,0.00001434075,0.4941038,0.0002220478,0.0007549624,0.0001679592],"study_design_candidate":"bench_or_experimental","study_design_consensus":null,"genre_codex":"empirical","genre_gemma":"empirical","genre_scores_codex":[0.9991491,0.0003851569,0.0001469665,0.00006601718,0.00004593919,0.00009712484,0.000001471286,7.981056e-7,0.0001073957],"genre_scores_gemma":[0.9985733,0.0005538447,0.0006324482,0.0001364272,0.00001377239,0.000002188513,0.000001675681,0.00001605775,0.00007025861],"genre_candidate":"empirical","genre_consensus":"empirical","teacher_disagreement_score":0.4352883,"threshold_uncertainty_score":0.2162466,"prediction_status":"machine_predicted_unvalidated"},"labels":[],"label_agreement":null},{"id":"W2069941412","doi":"10.1086/302909","title":"Coding and Noncoding Variation of the Human Calcium-Channel β4-Subunit Gene CACNB4 in Patients with Idiopathic Generalized Epilepsy and Episodic Ataxia","year":2000,"lang":"en","type":"article","venue":"The American Journal of Human Genetics","topic":"Ion channel regulation and function","field":"Biochemistry, Genetics and Molecular Biology","cited_by":417,"is_retracted":false,"has_abstract":false,"routes":{"ca_aff":true,"ca_fund":false,"ca_venue":false,"about_ca":false},"ca_institutions":"University of Manitoba","funders":"National Institute of Neurological Disorders and Stroke; National Institute on Deafness and Other Communication Disorders; National Institutes of Health","keywords":"Epilepsy; Ataxia; Calcium channel; Gene; Genetics; Idiopathic generalized epilepsy; Protein subunit; Coding (social sciences); Neuroscience; Biology; Psychology; Medicine; Calcium; Internal medicine; Mathematics","retraction":null,"screen_n_in":null,"score":{"opus":0.01247127046359207,"gpt":0.2396556549057562,"spread":0.2271843844421642,"validation_status":"score_only:v0-immature-baseline"},"prediction":{"model_version":"codex-gemma-dda1882f352a","candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0003485622,0.0001209234,0.000214123,0.00006573325,0.0001828911,0.00001949541,0.0001409184,0.00004035356,0.000008350147],"category_scores_gemma":[0.00001327975,0.00007697019,0.0000445528,0.0001324256,0.000278346,0.000007047906,0.00004413359,0.000124456,1.851307e-7],"about_ca_system_candidate":false,"about_ca_system_consensus":false,"about_ca_system_score_codex":0.00001787788,"about_ca_system_score_gemma":0.00002919976,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_topic_score_codex":0.00003525564,"about_ca_topic_score_gemma":0.00001597428,"domain_scores_codex":[0.9989917,0.000196098,0.0003600479,0.0001295404,0.0001889266,0.0001336398],"domain_scores_gemma":[0.9991403,0.000008545204,0.0004854872,0.0001841846,0.0001311594,0.00005032051],"domain_codex":null,"domain_gemma":null,"domain_candidate":null,"domain_consensus":null,"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","study_design_scores_codex":[0.001348359,0.0002707567,0.3126077,0.0000567153,0.0002495985,0.000004272044,0.003959561,0.0132086,0.6471627,0.0001369358,0.00009380838,0.02090097],"study_design_scores_gemma":[0.002466417,0.001903557,0.9724606,0.00009185278,0.00008748153,0.00004405446,0.0002412827,0.0007013151,0.02146904,0.0002046653,0.0001347898,0.0001948965],"study_design_candidate":"observational","study_design_consensus":null,"genre_codex":"empirical","genre_gemma":"empirical","genre_scores_codex":[0.9988315,0.0003596799,0.0005187868,0.00007860295,0.00005821773,0.000122321,0.000004426599,0.000001615732,0.00002483558],"genre_scores_gemma":[0.9992732,0.0002014073,0.0001258978,0.0001199439,0.0002003822,0.000001698162,0.000006453977,0.000016029,0.00005498384],"genre_candidate":"empirical","genre_consensus":"empirical","teacher_disagreement_score":0.659853,"threshold_uncertainty_score":0.3138753,"prediction_status":"machine_predicted_unvalidated"},"labels":[],"label_agreement":null},{"id":"W2033942199","doi":"10.1016/j.ajhg.2007.10.004","title":"TINF2, a Component of the Shelterin Telomere Protection Complex, Is Mutated in Dyskeratosis Congenita","year":2008,"lang":"en","type":"article","venue":"The American Journal of Human Genetics","topic":"Telomeres, Telomerase, and Senescence","field":"Medicine","cited_by":409,"is_retracted":false,"has_abstract":false,"routes":{"ca_aff":true,"ca_fund":false,"ca_venue":false,"about_ca":false},"ca_institutions":"Terry Fox Research Institute","funders":"National Institute of Allergy and Infectious Diseases; National Cancer Institute; National Institutes of Health","keywords":"Dyskeratosis congenita; Telomere; Shelterin; Component (thermodynamics); Telomere-binding protein; Genetics; Biology; DNA; Physics; DNA-binding protein; Gene","retraction":null,"screen_n_in":null,"score":{"opus":0.0527861258469614,"gpt":0.2878149480777267,"spread":0.2350288222307653,"validation_status":"score_only:v0-immature-baseline"},"prediction":{"model_version":"codex-gemma-dda1882f352a","candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0002751445,0.0001782573,0.0005724807,0.000180053,0.0001786524,0.00001030874,0.0003658181,0.00003046062,0.0001001932],"category_scores_gemma":[0.00003390367,0.0001061671,0.0001811853,0.0005735892,0.0009815844,0.00002997468,0.00006986925,0.0004211004,0.00000501739],"about_ca_system_candidate":false,"about_ca_system_consensus":false,"about_ca_system_score_codex":0.00007872577,"about_ca_system_score_gemma":0.0001418006,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_topic_score_codex":0.0001876316,"about_ca_topic_score_gemma":0.0000283288,"domain_scores_codex":[0.9981367,0.0002334049,0.0007560591,0.0001361183,0.0004973344,0.0002404004],"domain_scores_gemma":[0.9983166,0.00005031728,0.00084389,0.0004143246,0.0002725123,0.0001023095],"domain_codex":null,"domain_gemma":null,"domain_candidate":null,"domain_consensus":null,"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","study_design_scores_codex":[0.0008790544,0.000562267,0.1208159,0.0000753647,0.0002897657,0.0001326925,0.01011715,0.0001842783,0.8513847,0.00001606991,0.001064282,0.01447845],"study_design_scores_gemma":[0.001701698,0.002162748,0.9073459,0.0001962056,0.0001217286,0.001928522,0.001832127,0.0004009393,0.08321549,0.00007520363,0.0008385455,0.0001809285],"study_design_candidate":"observational","study_design_consensus":null,"genre_codex":"empirical","genre_gemma":"empirical","genre_scores_codex":[0.997795,0.0003451807,0.0000509508,0.001223018,0.00008143306,0.0003633473,0.000008049305,0.00000875864,0.0001242784],"genre_scores_gemma":[0.9984722,0.0003026004,0.0004237137,0.0005879756,0.0001100266,0.000004293401,0.000001218101,0.00002454752,0.0000734435],"genre_candidate":"empirical","genre_consensus":"empirical","teacher_disagreement_score":0.78653,"threshold_uncertainty_score":0.4329367,"prediction_status":"machine_predicted_unvalidated"},"labels":[],"label_agreement":null},{"id":"W2158488248","doi":"10.1016/j.ajhg.2010.08.006","title":"Mutability of Y-Chromosomal Microsatellites: Rates, Characteristics, Molecular Bases, and Forensic Implications","year":2010,"lang":"en","type":"article","venue":"The American Journal of Human Genetics","topic":"Forensic and Genetic Research","field":"Biochemistry, Genetics and Molecular Biology","cited_by":408,"is_retracted":false,"has_abstract":false,"routes":{"ca_aff":true,"ca_fund":false,"ca_venue":false,"about_ca":false},"ca_institutions":"Université du Québec à Chicoutimi; Université de Montréal; Centre Hospitalier Universitaire Sainte-Justine","funders":"","keywords":"Microsatellite; Forensic science; Genetics; Evolutionary biology; Biology; Forensic genetics; Computational biology; Gene; Allele","retraction":null,"screen_n_in":null,"score":{"opus":0.00973837411371886,"gpt":0.298493366799123,"spread":0.2887549926854041,"validation_status":"score_only:v0-immature-baseline"},"prediction":{"model_version":"codex-gemma-dda1882f352a","candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0004359258,0.0001357074,0.0002732934,0.00004784447,0.00009582903,0.00002482654,0.0003708998,0.00004631669,0.00001693058],"category_scores_gemma":[0.000107257,0.00009915039,0.0001098245,0.0001015298,0.001687105,0.000002419272,0.0001301172,0.0002322965,9.655262e-7],"about_ca_system_candidate":false,"about_ca_system_consensus":false,"about_ca_system_score_codex":0.000005316536,"about_ca_system_score_gemma":0.0001234147,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_topic_score_codex":0.00001849154,"about_ca_topic_score_gemma":0.0000193795,"domain_scores_codex":[0.9988846,0.0001080107,0.0004579968,0.0001712194,0.0001682136,0.0002099939],"domain_scores_gemma":[0.9983993,0.00004330448,0.0004922625,0.0005319859,0.00041045,0.000122723],"domain_codex":null,"domain_gemma":null,"domain_candidate":null,"domain_consensus":null,"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","study_design_scores_codex":[0.00005760606,0.0000480639,0.02209886,0.00001043473,0.00005976195,0.0000024375,0.00006171584,0.00000430806,0.9510087,0.0001665407,0.0001238948,0.02635761],"study_design_scores_gemma":[0.0002805287,0.001837313,0.2270659,0.00001169154,0.00006576898,0.0002595462,0.0001817874,0.00001698507,0.7663964,0.001423935,0.002303127,0.0001570441],"study_design_candidate":"bench_or_experimental","study_design_consensus":"bench_or_experimental","genre_codex":"empirical","genre_gemma":"empirical","genre_scores_codex":[0.9981452,0.0007984992,0.0004978238,0.0002857385,0.00006313152,0.0001157703,0.00003469435,0.000001665907,0.00005751623],"genre_scores_gemma":[0.9958476,0.000426481,0.003346187,0.0001407338,0.0001759635,0.000002328058,0.00001808263,0.00001953901,0.00002305195],"genre_candidate":"empirical","genre_consensus":"empirical","teacher_disagreement_score":0.204967,"threshold_uncertainty_score":0.621621,"prediction_status":"machine_predicted_unvalidated"},"labels":[],"label_agreement":null},{"id":"W2032602115","doi":"10.1016/j.ajhg.2013.10.004","title":"Global Analysis of DNA Methylation Variation in Adipose Tissue from Twins Reveals Links to Disease-Associated Variants in Distal Regulatory Elements","year":2013,"lang":"en","type":"article","venue":"The American Journal of Human Genetics","topic":"Epigenetics and DNA Methylation","field":"Biochemistry, Genetics and Molecular Biology","cited_by":398,"is_retracted":false,"has_abstract":true,"routes":{"ca_aff":true,"ca_fund":true,"ca_venue":false,"about_ca":false},"ca_institutions":"McGill University and Génome Québec Innovation Centre","funders":"Canadian Institutes of Health Research; National Institute for Health and Care Research; Wellcome Trust","keywords":"DNA methylation; Adipose tissue; Biology; Genetics; Computational biology; Variation (astronomy); Gene; Gene expression; Endocrinology","retraction":null,"screen_n_in":null,"score":{"opus":0.01030190908691403,"gpt":0.2850802118448802,"spread":0.2747783027579662,"validation_status":"score_only:v0-immature-baseline"},"prediction":{"model_version":"codex-gemma-dda1882f352a","candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0006327115,0.0001329271,0.000364961,0.0001777867,0.00003661054,0.00002428728,0.0002732009,0.00007305692,0.000025591],"category_scores_gemma":[0.00013598,0.0001159491,0.0001092956,0.0007387017,0.00006966905,0.000008161745,0.00007132957,0.0001047994,0.000001226935],"about_ca_system_candidate":false,"about_ca_system_consensus":false,"about_ca_system_score_codex":0.00008455432,"about_ca_system_score_gemma":0.0000742196,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_topic_score_codex":0.0003452762,"about_ca_topic_score_gemma":0.0006650732,"domain_scores_codex":[0.9981422,0.0003927398,0.0007996063,0.0001903464,0.0002915406,0.0001835455],"domain_scores_gemma":[0.9983865,0.00003694809,0.0009073047,0.0003267607,0.000224532,0.0001179278],"domain_codex":null,"domain_gemma":null,"domain_candidate":null,"domain_consensus":null,"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","study_design_scores_codex":[0.00007210611,0.0001526891,0.3544795,0.000002092379,0.0003918519,0.000001949391,0.0003069527,0.01107578,0.6278632,0.00001269516,0.00001925397,0.005621863],"study_design_scores_gemma":[0.0003723797,0.0005141784,0.9881809,0.00002056698,0.0003657266,1.6142e-7,0.00007922079,0.0006632124,0.008236188,0.001431942,0.00001750082,0.0001180723],"study_design_candidate":"observational","study_design_consensus":null,"genre_codex":"empirical","genre_gemma":"empirical","genre_scores_codex":[0.9969193,0.0007069345,0.001924064,0.0001025433,0.00005133711,0.0001990765,0.00007200958,0.000001518072,0.00002325781],"genre_scores_gemma":[0.9986444,0.000105705,0.0009677889,0.00008547854,0.00007785544,0.00000509102,0.00008642008,0.0000126263,0.00001467506],"genre_candidate":"empirical","genre_consensus":"empirical","teacher_disagreement_score":0.6337013,"threshold_uncertainty_score":0.4728266,"prediction_status":"machine_predicted_unvalidated"},"labels":[],"label_agreement":null},{"id":"W2906821085","doi":"10.1016/j.ajhg.2018.11.014","title":"Integrating Genomics into Healthcare: A Global Responsibility","year":2019,"lang":"en","type":"article","venue":"The American Journal of Human Genetics","topic":"Genomics and Rare Diseases","field":"Biochemistry, Genetics and Molecular Biology","cited_by":395,"is_retracted":false,"has_abstract":false,"routes":{"ca_aff":true,"ca_fund":false,"ca_venue":false,"about_ca":false},"ca_institutions":"Ontario Genomics; Ontario Institute for Cancer Research","funders":"Medical Research Council; National Institute for Health and Care Research; Health Data Research UK; National Health and Medical Research Council; Australian Genomics Health Alliance; Cancer Research UK; Wellcome Trust","keywords":"Transformative learning; Government (linguistics); Health care; Precision medicine; Data sharing; Diversity (politics); Genomics; Business; Personalized medicine; Political science; Economic growth; Medicine; Bioinformatics; Sociology; Biology; Genome; Alternative medicine; Economics","retraction":null,"screen_n_in":null,"score":{"opus":0.008103850877362772,"gpt":0.2919829303738561,"spread":0.2838790794964934,"validation_status":"score_only:v0-immature-baseline"},"prediction":{"model_version":"codex-gemma-dda1882f352a","candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0004691567,0.000137134,0.0002406833,0.0000276637,0.0001139828,0.00003460231,0.0004920037,0.00003340891,0.000008569267],"category_scores_gemma":[0.00004956121,0.00009588604,0.0001762287,0.0001072352,0.0002393336,0.000002110482,0.0001496656,0.0001399182,0.000007066507],"about_ca_system_candidate":false,"about_ca_system_consensus":false,"about_ca_system_score_codex":0.00007100612,"about_ca_system_score_gemma":0.0003201879,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_topic_score_codex":0.00005347798,"about_ca_topic_score_gemma":0.00006584692,"domain_scores_codex":[0.9988681,0.0002007727,0.0003982314,0.0001736901,0.0001572693,0.0002019447],"domain_scores_gemma":[0.9986313,0.00001946533,0.0005356389,0.000468307,0.0002218066,0.0001234936],"domain_codex":null,"domain_gemma":null,"domain_candidate":null,"domain_consensus":null,"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","study_design_scores_codex":[0.001178239,0.0001588783,0.0792842,0.00003385871,0.0002707535,0.00002212703,0.0008412864,0.0006091652,0.8819431,0.0006388982,0.0009914166,0.0340281],"study_design_scores_gemma":[0.006780477,0.05458338,0.6353141,0.0002968256,0.0007469549,0.00349687,0.02980365,0.0008338919,0.1171097,0.05003376,0.09775921,0.003241158],"study_design_candidate":"bench_or_experimental","study_design_consensus":null,"genre_codex":"empirical","genre_gemma":"empirical","genre_scores_codex":[0.9968196,0.002002405,0.000267166,0.0004929582,0.0001671132,0.0001139751,0.00001293754,0.000002654531,0.0001212086],"genre_scores_gemma":[0.9965757,0.0002411967,0.002057467,0.0007585837,0.0002999639,9.817545e-7,0.000006619252,0.00001644881,0.0000430238],"genre_candidate":"empirical","genre_consensus":"empirical","teacher_disagreement_score":0.7648334,"threshold_uncertainty_score":0.3910119,"prediction_status":"machine_predicted_unvalidated"},"labels":[],"label_agreement":null},{"id":"W2011094690","doi":"10.1086/424388","title":"Integrated Evaluation of DNA Sequence Variants of Unknown Clinical Significance: Application to BRCA1 and BRCA2","year":2004,"lang":"en","type":"article","venue":"The American Journal of Human Genetics","topic":"BRCA gene mutations in cancer","field":"Biochemistry, Genetics and Molecular Biology","cited_by":385,"is_retracted":false,"has_abstract":false,"routes":{"ca_aff":false,"ca_fund":true,"ca_venue":false,"about_ca":false},"ca_institutions":"","funders":"National Cancer Institute; Medical Research and Materiel Command; Canadian Institutes of Health Research; National Institutes of Health; Breast Cancer Research Foundation","keywords":"Genetics; Clinical significance; Biology; Sequence (biology); Disease; Family history; Computational biology; DNA sequencing; Gene; Bioinformatics; Medicine; Internal medicine","retraction":null,"screen_n_in":null,"score":{"opus":0.047699188417183,"gpt":0.383924855429786,"spread":0.336225667012603,"validation_status":"score_only:v0-immature-baseline"},"prediction":{"model_version":"codex-gemma-dda1882f352a","candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.001447083,0.0001001759,0.0002485197,0.00006278347,0.00004522701,0.000008314017,0.0003233466,0.00004241982,0.000005459554],"category_scores_gemma":[0.0001556344,0.00007841782,0.00007038387,0.0002304832,0.0005518168,0.000003526507,0.00005572934,0.0001108453,7.362552e-7],"about_ca_system_candidate":false,"about_ca_system_consensus":false,"about_ca_system_score_codex":0.00007167935,"about_ca_system_score_gemma":0.000595345,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_topic_score_codex":0.00002918191,"about_ca_topic_score_gemma":0.0000276362,"domain_scores_codex":[0.9985278,0.0002343194,0.0006402606,0.0001670233,0.0003235666,0.0001070628],"domain_scores_gemma":[0.9977316,0.00002988613,0.0009013559,0.0003538112,0.000915286,0.00006809078],"domain_codex":null,"domain_gemma":null,"domain_candidate":null,"domain_consensus":null,"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","study_design_scores_codex":[0.0001077814,0.00007347995,0.001465281,0.000006640503,0.0001075274,3.283502e-7,0.0003526055,0.01063582,0.9179466,0.00008407555,0.00008186005,0.06913802],"study_design_scores_gemma":[0.002400524,0.006598796,0.1436031,0.000113872,0.0005422283,0.0001017732,0.00164734,0.0006821048,0.8378562,0.004746231,0.001373915,0.0003338879],"study_design_candidate":"bench_or_experimental","study_design_consensus":"bench_or_experimental","genre_codex":"empirical","genre_gemma":"empirical","genre_scores_codex":[0.9878591,0.000549617,0.0110052,0.0002279629,0.00007049816,0.0002209383,0.00001284638,0.000001466075,0.00005240343],"genre_scores_gemma":[0.9936214,0.0002932986,0.005760335,0.0001404545,0.0001487762,0.000007863498,0.000006779888,0.00001417413,0.000006932395],"genre_candidate":"empirical","genre_consensus":"empirical","teacher_disagreement_score":0.1421378,"threshold_uncertainty_score":0.3197786,"prediction_status":"machine_predicted_unvalidated"},"labels":[],"label_agreement":null},{"id":"W1975365119","doi":"10.1086/318809","title":"A Phase 1/2 Clinical Trial of Enzyme Replacement in Fabry Disease: Pharmacokinetic, Substrate Clearance, and Safety Studies","year":2001,"lang":"en","type":"article","venue":"The American Journal of Human Genetics","topic":"Lysosomal Storage Disorders Research","field":"Medicine","cited_by":383,"is_retracted":false,"has_abstract":false,"routes":{"ca_aff":false,"ca_fund":true,"ca_venue":false,"about_ca":false},"ca_institutions":"","funders":"Eunice Kennedy Shriver National Institute of Child Health and Human Development; National Institute of Diabetes and Digestive and Kidney Diseases; National Center for Research Resources; McGill University","keywords":"Pharmacokinetics; Medicine; Enzyme replacement therapy; Globotriaosylceramide; Kidney; Fabry disease; Internal medicine; Clearance; Pharmacology; Endocrinology; Pathology; Gastroenterology; Urology; Disease","retraction":null,"screen_n_in":null,"score":{"opus":0.1037982530427376,"gpt":0.4664230837248811,"spread":0.3626248306821435,"validation_status":"score_only:v0-immature-baseline"},"prediction":{"model_version":"codex-gemma-dda1882f352a","candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.001507895,0.0001394295,0.0007119161,0.0001459511,0.00006499211,0.00001054855,0.0002107534,0.00001895802,0.00004500674],"category_scores_gemma":[0.0002282667,0.0000928864,0.0001500213,0.0003013071,0.001104617,0.0000298056,0.00008126098,0.0004107767,0.000001377258],"about_ca_system_candidate":false,"about_ca_system_consensus":false,"about_ca_system_score_codex":0.00005174318,"about_ca_system_score_gemma":0.000149474,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_topic_score_codex":0.000008899132,"about_ca_topic_score_gemma":0.000006539055,"domain_scores_codex":[0.9975209,0.0004206356,0.001094349,0.0001632628,0.0005523707,0.0002485327],"domain_scores_gemma":[0.9983219,0.0002274663,0.0006899539,0.0002788722,0.0002574594,0.0002243283],"domain_codex":null,"domain_gemma":null,"domain_candidate":null,"domain_consensus":null,"study_design_codex":"randomized_trial","study_design_gemma":"randomized_trial","study_design_scores_codex":[0.6564882,0.00573668,0.08608264,0.0001457103,0.001178904,0.0009893527,0.002077428,0.0001747521,0.005413474,0.00003710067,0.001201364,0.2404744],"study_design_scores_gemma":[0.4656124,0.1033435,0.4079765,0.0007803505,0.001489458,0.0005080276,0.009065486,0.00113103,0.001520541,0.0008409346,0.007162869,0.0005687715],"study_design_candidate":"randomized_trial","study_design_consensus":"randomized_trial","genre_codex":"empirical","genre_gemma":"empirical","genre_scores_codex":[0.989272,0.008989505,0.00004542999,0.001047244,0.00008906598,0.0004453727,0.000004067578,0.000003838432,0.0001034756],"genre_scores_gemma":[0.9740477,0.0251609,0.0001302572,0.000214135,0.0003143059,0.000004397152,0.000001009838,0.00001803887,0.0001092582],"genre_candidate":"empirical","genre_consensus":"empirical","teacher_disagreement_score":0.3218939,"threshold_uncertainty_score":0.4070008,"prediction_status":"machine_predicted_unvalidated"},"labels":[],"label_agreement":null},{"id":"W2098207011","doi":"10.1016/j.ajhg.2009.06.022","title":"Massively Parallel Sequencing: The Next Big Thing in Genetic Medicine","year":2009,"lang":"en","type":"review","venue":"The American Journal of Human Genetics","topic":"Genomics and Rare Diseases","field":"Biochemistry, Genetics and Molecular Biology","cited_by":381,"is_retracted":false,"has_abstract":false,"routes":{"ca_aff":true,"ca_fund":true,"ca_venue":false,"about_ca":false},"ca_institutions":"Child and Family Research Institute; BC Cancer Agency; University of British Columbia","funders":"Canadian Institutes of Health Research","keywords":"Massive parallel sequencing; Massively parallel; Sanger sequencing; Computer science; DNA sequencing; Personal genomics; Genomics; Computational biology; Biology; Genetics; Genome; Parallel computing; Gene","retraction":null,"screen_n_in":null,"score":{"opus":0.07029077671750361,"gpt":0.3345144717670009,"spread":0.2642236950494973,"validation_status":"score_only:v0-immature-baseline"},"prediction":{"model_version":"codex-gemma-dda1882f352a","candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0005732864,0.0004162992,0.001200995,0.000159661,0.0001739876,0.00005663012,0.0014258,0.0001028228,0.000008517075],"category_scores_gemma":[0.00007254577,0.0002096306,0.0004923578,0.0002566352,0.000641362,0.000001986401,0.0001617063,0.0005316922,0.000003470927],"about_ca_system_candidate":false,"about_ca_system_consensus":false,"about_ca_system_score_codex":0.00007652399,"about_ca_system_score_gemma":0.000592665,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_topic_score_codex":0.00002151432,"about_ca_topic_score_gemma":0.00001861308,"domain_scores_codex":[0.9974909,0.0005051397,0.001058744,0.0002747693,0.0003075578,0.000362856],"domain_scores_gemma":[0.9970962,0.00007502529,0.001862967,0.0006932546,0.0001393036,0.0001332198],"domain_codex":null,"domain_gemma":null,"domain_candidate":null,"domain_consensus":null,"study_design_codex":"design_other","study_design_gemma":"not_applicable","study_design_scores_codex":[0.00003310641,0.00004327795,0.00003040607,0.0002313089,0.0003227561,0.0001506204,0.0003367088,0.0003352145,0.0008663172,0.00001818382,0.001017895,0.9966142],"study_design_scores_gemma":[0.0005355151,0.003010637,0.0008501597,0.00264873,0.001403122,0.001863572,0.001357164,0.00001200778,0.00002335078,0.0006369957,0.9870383,0.0006204896],"study_design_candidate":"design_other","study_design_consensus":null,"genre_codex":"review","genre_gemma":"review","genre_scores_codex":[0.03131054,0.9678366,0.0001053444,0.0002028792,0.0001652314,0.0002684568,0.000007178909,0.000002399611,0.0001014023],"genre_scores_gemma":[0.0189369,0.9784018,0.0003460126,0.0005824305,0.001557572,0.000006879111,0.00001698754,0.00005763331,0.00009379628],"genre_candidate":"review","genre_consensus":"review","teacher_disagreement_score":0.9959937,"threshold_uncertainty_score":0.8548486,"prediction_status":"machine_predicted_unvalidated"},"labels":[],"label_agreement":null},{"id":"W2079477526","doi":"10.1086/323123","title":"p63 Gene Mutations in EEC Syndrome, Limb-Mammary Syndrome, and Isolated Split Hand–Split Foot Malformation Suggest a Genotype-Phenotype Correlation","year":2001,"lang":"en","type":"article","venue":"The American Journal of Human Genetics","topic":"Cancer-related Molecular Pathways","field":"Medicine","cited_by":378,"is_retracted":false,"has_abstract":false,"routes":{"ca_aff":true,"ca_fund":false,"ca_venue":false,"about_ca":false},"ca_institutions":"University of Toronto","funders":"Nederlandse Organisatie voor Wetenschappelijk Onderzoek","keywords":"Ectrodactyly; Missense mutation; Exon; Genetics; Nonsense mutation; Biology; Mutation; Hypoplasia; Frameshift mutation; Syndactyly; Gene; Ectodermal dysplasia; Anatomy","retraction":null,"screen_n_in":null,"score":{"opus":0.01136954219852511,"gpt":0.2509902373753706,"spread":0.2396206951768455,"validation_status":"score_only:v0-immature-baseline"},"prediction":{"model_version":"codex-gemma-dda1882f352a","candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0004193482,0.0002249013,0.0005052267,0.0004554826,0.0001975642,0.0000667737,0.0002120101,0.00008311963,0.00003961612],"category_scores_gemma":[0.00006380428,0.00018971,0.0001023925,0.0008675127,0.0003407141,0.0001321009,0.0000648034,0.0005319091,0.00001884896],"about_ca_system_candidate":false,"about_ca_system_consensus":false,"about_ca_system_score_codex":0.0001985935,"about_ca_system_score_gemma":0.0002249179,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_topic_score_codex":0.00006656743,"about_ca_topic_score_gemma":0.0000508914,"domain_scores_codex":[0.9981292,0.0001454533,0.0008141267,0.0001917089,0.0004022221,0.0003172757],"domain_scores_gemma":[0.9982217,0.00007766083,0.0008037287,0.0003875955,0.0003237106,0.0001855971],"domain_codex":null,"domain_gemma":null,"domain_candidate":null,"domain_consensus":null,"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","study_design_scores_codex":[0.008675807,0.002762145,0.1384967,0.0005488276,0.003685548,0.01558052,0.03033348,0.06907263,0.4816015,0.00217968,0.001119103,0.2459441],"study_design_scores_gemma":[0.003850269,0.01012415,0.926569,0.0004086813,0.0007871325,0.04115476,0.0007761672,0.01318044,0.0009100864,0.000987886,0.0007563601,0.0004950159],"study_design_candidate":"observational","study_design_consensus":null,"genre_codex":"empirical","genre_gemma":"empirical","genre_scores_codex":[0.98791,0.00268596,0.008056108,0.0006066023,0.0001319335,0.0003756837,0.000006774671,0.00002150572,0.0002054564],"genre_scores_gemma":[0.9956067,0.001157605,0.002715389,0.0002415129,0.00006564314,0.000006531748,0.0000376434,0.00004684342,0.0001221603],"genre_candidate":"empirical","genre_consensus":"empirical","teacher_disagreement_score":0.7880723,"threshold_uncertainty_score":0.7736148,"prediction_status":"machine_predicted_unvalidated"},"labels":[],"label_agreement":null}]}