{"meta":{"page":1,"per_page":50,"max_per_page":100,"total":123,"total_is_capped":false,"direct_labels_cover":0,"predictions_cover":123,"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","author_layer_release":"2026-06-26"},"query_hash":"c1041d621ecc","filters":{"venue":"BMC Medical Genetics"}},"results":[{"id":"W2168394145","doi":"10.1186/1471-2350-7-1","title":"Mutation analysis of SDHB and SDHC: novel germline mutations in sporadic head and neck paraganglioma and familial paraganglioma and/or pheochromocytoma","year":2006,"lang":"en","type":"article","venue":"BMC Medical Genetics","topic":"Adrenal and Paraganglionic Tumors","field":"Medicine","cited_by":167,"is_retracted":false,"has_abstract":true,"routes":{"ca_aff":true,"ca_fund":false,"ca_venue":false,"about_ca":false},"ca_institutions":"McGill University; Jewish General Hospital","funders":"Regione Piemonte; Associazione Italiana per la Ricerca sul Cancro; KWF Kankerbestrijding; Compagnia di San Paolo","keywords":"SDHB; SDHD; Paraganglioma; SDHA; Germline mutation; Pheochromocytoma; Biology; Missense mutation; Genetics; Germline; Exon; Molecular biology; Mutation; Succinate dehydrogenase; Gene; Endocrinology; Medicine; Pathology; Mitochondrion","authors":[{"name":"Jean‐Pierre Bayley","is_ca":false},{"name":"Ivonne van Minderhout","is_ca":false},{"name":"Marjan M. Weiss","is_ca":false},{"name":"Jeroen C. Jansen","is_ca":false},{"name":"P. H. N. Oomen","is_ca":false},{"name":"Fred H. Menko","is_ca":false},{"name":"Barbara Pasini","is_ca":false},{"name":"Barbara Ferrando","is_ca":false},{"name":"Nora Wong","is_ca":true},{"name":"Lesley Alpert","is_ca":true},{"name":"Rosie S. Williams","is_ca":false},{"name":"Edward Blair","is_ca":false},{"name":"Peter Devilee","is_ca":false},{"name":"Peter E.M. Taschner","is_ca":false}],"retraction":null,"screen_n_in":null,"score":{"opus":0.02309886869761124,"gpt":0.300975062427017,"spread":0.2778761937294058,"validation_status":"score_only:v0-immature-baseline"},"prediction":{"model_version":"metacan-v3-hybrid-931329e0061c","candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0001221808,0.0005163988,0.0002262449,0.001013487,0.0004308665,0.0002339374,0.0002504006,0.0004928473,0.001181587],"category_scores_gemma":[0.0006204277,0.0001895093,0.000232566,0.0003670324,0.0003998295,0.0001145109,0.0003120343,0.0002057993,0.0001522906],"about_ca_system_candidate":false,"about_ca_system_consensus":false,"about_ca_system_score_codex":0.0003039064,"about_ca_system_score_gemma":0.0002656481,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_topic_score_codex":0.002316362,"about_ca_topic_score_gemma":0.002433721,"domain_scores_codex":[0.9998164,0.00001484829,0.00001876486,0.00005416614,0.00005638896,0.00003953948],"domain_scores_gemma":[0.9996897,0.00009470089,0.00006224712,0.00001379098,0.00003889757,0.0001007335],"domain_codex":null,"domain_gemma":null,"domain_candidate":null,"domain_consensus":null,"study_design_codex":"observational","study_design_gemma":"observational","study_design_scores_codex":[0.0004874213,0.0001774605,0.621201,0.000125853,0.0002237329,0.1917927,0.001957684,0.0005200849,0.1709787,0.0001824993,0.0003260566,0.01202683],"study_design_scores_gemma":[0.0001141598,0.0006070481,0.6910579,0.00002039897,0.000195732,0.2791063,0.0006556104,0.001342321,0.02524642,0.0002008847,0.001415925,0.0000373813],"study_design_candidate":"observational","study_design_consensus":"observational","genre_codex":"empirical","genre_gemma":"empirical","genre_scores_codex":[0.9996089,0.00008214813,0.00012213,0.00001086817,0.000002447336,0.000004812061,0.00003121919,0.000004899274,0.0001325482],"genre_scores_gemma":[0.9997161,0.00002529626,0.000123438,0.000007971946,0.000003594403,0.000002594441,0.00004509452,0.000001531742,0.00007438254],"genre_candidate":"empirical","genre_consensus":"empirical","teacher_disagreement_score":0.002316362,"threshold_uncertainty_score":0.00460577,"prediction_status":"machine_predicted_unvalidated"},"labels":[],"label_agreement":null},{"id":"W2135748243","doi":"10.1186/s12881-015-0174-1","title":"Leptin and adiponectin DNA methylation levels in adipose tissues and blood cells are associated with BMI, waist girth and LDL-cholesterol levels in severely obese men and women","year":2015,"lang":"en","type":"article","venue":"BMC Medical Genetics","topic":"Adipokines, Inflammation, and Metabolic Diseases","field":"Medicine","cited_by":141,"is_retracted":false,"has_abstract":true,"routes":{"ca_aff":true,"ca_fund":true,"ca_venue":false,"about_ca":false},"ca_institutions":"Université Laval; Cégep de Sherbrooke; Cégep de Chicoutimi; Centre hospitalier universitaire de Québec; Université de Sherbrooke","funders":"Fonds de Recherche du Québec - Santé; Canadian Institutes of Health Research; Canadian Diabetes Association; Institut universitaire de cardiologie et de pneumologie de Québec, Université Laval; American Diabetes Association; American Heart Association; Université de Sherbrooke","keywords":"DNA methylation; Adiponectin; Endocrinology; Internal medicine; Adipose tissue; Adipokine; Leptin; Biology; Methylation; Epigenetics; CpG site; Body mass index; Obesity; Medicine; Insulin resistance; Genetics; Gene; Gene expression","authors":[{"name":"Andrée-Anne Houde","is_ca":true},{"name":"Cécilia Légaré","is_ca":true},{"name":"Simon Biron","is_ca":true},{"name":"Odette Lescelleur","is_ca":true},{"name":"Laurent Biertho","is_ca":true},{"name":"Simon Marceau","is_ca":true},{"name":"André Tchernof","is_ca":true},{"name":"Marie‐Claude Vohl","is_ca":true},{"name":"Marie‐France Hivert","is_ca":true},{"name":"Luigi Bouchard","is_ca":true}],"retraction":null,"screen_n_in":null,"score":{"opus":0.03603932563401342,"gpt":0.2746058121914565,"spread":0.2385664865574431,"validation_status":"score_only:v0-immature-baseline"},"prediction":{"model_version":"metacan-v3-hybrid-931329e0061c","candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0001393444,0.0001566171,0.0001813221,0.0003895849,0.0001915527,0.0002264797,0.0001049134,0.0002135023,0.001330598],"category_scores_gemma":[0.0004775806,0.0002048998,0.0001858598,0.0003469996,0.0001809429,0.00007996469,0.0001837653,0.0002220661,0.0001428453],"about_ca_system_candidate":false,"about_ca_system_consensus":false,"about_ca_system_score_codex":0.00006664429,"about_ca_system_score_gemma":0.00006176234,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_topic_score_codex":0.001004069,"about_ca_topic_score_gemma":0.001293627,"domain_scores_codex":[0.9999062,0.0000195857,0.00001175431,0.00003379825,0.00001391221,0.00001473579],"domain_scores_gemma":[0.9997655,0.00005090295,0.0001088804,0.00001638849,0.00001589192,0.00004244932],"domain_codex":null,"domain_gemma":null,"domain_candidate":null,"domain_consensus":null,"study_design_codex":"observational","study_design_gemma":"observational","study_design_scores_codex":[0.0006133774,0.00001569146,0.9852751,0.0000137945,0.00007534521,0.0001243063,0.0001456066,0.00004076627,0.01142373,0.00001542598,0.00003723348,0.002219509],"study_design_scores_gemma":[0.000004849118,0.00007580921,0.9989055,0.000002072337,0.00002840851,0.0003603932,0.00007700561,0.00006988936,0.0003887377,0.00001688096,0.00006871462,0.000001620034],"study_design_candidate":"observational","study_design_consensus":"observational","genre_codex":"empirical","genre_gemma":"empirical","genre_scores_codex":[0.9994816,0.0002155886,0.0000972473,0.00001218529,0.000001385277,0.000001981583,0.00007513908,0.000002123873,0.0001127714],"genre_scores_gemma":[0.9995794,0.00007013072,0.00009068349,0.0000103327,0.00000273702,0.00000399569,0.0000913996,0.000001018468,0.0001503579],"genre_candidate":"empirical","genre_consensus":"empirical","teacher_disagreement_score":0.001330598,"threshold_uncertainty_score":0.004451275,"prediction_status":"machine_predicted_unvalidated"},"labels":[],"label_agreement":null},{"id":"W2140484686","doi":"10.1186/1471-2350-15-2","title":"Genome-wide association study of bipolar disorder in Canadian and UK populations corroborates disease loci including SYNE1 and CSMD1","year":2014,"lang":"en","type":"article","venue":"BMC Medical Genetics","topic":"Genetic Associations and Epidemiology","field":"Biochemistry, Genetics and Molecular Biology","cited_by":114,"is_retracted":false,"has_abstract":true,"routes":{"ca_aff":true,"ca_fund":true,"ca_venue":false,"about_ca":true},"ca_institutions":"Public Health Ontario; Hospital for Sick Children; Centre for Addiction and Mental Health; Cancer Care Ontario; SickKids Foundation; University of Toronto","funders":"Canadian Institutes of Health Research; Génome Québec; McGill University; GlaxoSmithKline","keywords":"Genome-wide association study; Biology; Genetics; Genetic association; Single-nucleotide polymorphism; Bipolar disorder; Gene; Genotype; Neuroscience","authors":[{"name":"Wei Xu","is_ca":true},{"name":"Sarah Cohen‐Woods","is_ca":false},{"name":"Qian Chen","is_ca":true},{"name":"Abdul Noor","is_ca":true},{"name":"Jo Knight","is_ca":true},{"name":"Georgina M. Hosang","is_ca":false},{"name":"Sagar V. Parikh","is_ca":true},{"name":"Vincenzo De Luca","is_ca":true},{"name":"Federica Tozzi","is_ca":false},{"name":"Pierandrea Muglia","is_ca":false},{"name":"Julia Forte","is_ca":false},{"name":"Andrew McQuillin","is_ca":false},{"name":"Pingzhao Hu","is_ca":true},{"name":"Hugh Gurling","is_ca":false},{"name":"James L. Kennedy","is_ca":true},{"name":"Peter McGuffin","is_ca":false},{"name":"Anne Farmer","is_ca":false},{"name":"John S. Strauss","is_ca":true},{"name":"John B. Vincent","is_ca":true}],"retraction":null,"screen_n_in":null,"score":{"opus":0.02065712771071314,"gpt":0.2838261362177238,"spread":0.2631690085070106,"validation_status":"score_only:v0-immature-baseline"},"prediction":{"model_version":"metacan-v3-hybrid-931329e0061c","candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.001012394,0.0005237365,0.000410728,0.001282658,0.002274404,0.0008367267,0.0005619352,0.0004550109,0.005520713],"category_scores_gemma":[0.002340641,0.0002086639,0.0006632436,0.002495779,0.0005851363,0.0001465696,0.0006872461,0.0006417591,0.0003303067],"about_ca_system_candidate":false,"about_ca_system_consensus":false,"about_ca_system_score_codex":0.003654474,"about_ca_system_score_gemma":0.005545079,"about_ca_topic_candidate":true,"about_ca_topic_consensus":true,"about_ca_topic_score_codex":0.7885007,"about_ca_topic_score_gemma":0.8926699,"domain_scores_codex":[0.9991541,0.00007344219,0.00004959396,0.0002884637,0.0002477762,0.0001867456],"domain_scores_gemma":[0.9986765,0.0001709467,0.0002387819,0.0001050937,0.0005812417,0.000227471],"domain_codex":null,"domain_gemma":null,"domain_candidate":null,"domain_consensus":null,"study_design_codex":"observational","study_design_gemma":"observational","study_design_scores_codex":[0.0009043728,0.00004691271,0.9632459,0.0001275271,0.0006768286,0.001138582,0.000898227,0.0002305923,0.009770701,0.0005136539,0.003854944,0.01859174],"study_design_scores_gemma":[0.00004286951,0.00002746104,0.9950613,0.00003748736,0.0002566978,0.000533156,0.0002809472,0.0001331619,0.0007400095,0.00009056792,0.002784068,0.00001233218],"study_design_candidate":"observational","study_design_consensus":"observational","genre_codex":"empirical","genre_gemma":"empirical","genre_scores_codex":[0.9824897,0.00301279,0.001050816,0.0007723111,0.00006383227,0.00004364259,0.00508339,0.00006000851,0.007423396],"genre_scores_gemma":[0.9944974,0.0009241095,0.001051891,0.0002322572,0.00001604364,0.00001607063,0.001860359,0.00001785969,0.001384165],"genre_candidate":"empirical","genre_consensus":"empirical","teacher_disagreement_score":0.2114993,"threshold_uncertainty_score":0.4254898,"prediction_status":"machine_predicted_unvalidated"},"labels":[],"label_agreement":null},{"id":"W2043884262","doi":"10.1186/1471-2350-13-26","title":"Mutations in LRP5 cause primary osteoporosis without features of OI by reducing Wnt signaling activity","year":2012,"lang":"en","type":"article","venue":"BMC Medical Genetics","topic":"Connective tissue disorders research","field":"Biochemistry, Genetics and Molecular Biology","cited_by":105,"is_retracted":false,"has_abstract":true,"routes":{"ca_aff":true,"ca_fund":false,"ca_venue":false,"about_ca":false},"ca_institutions":"SickKids Foundation; Hospital for Sick Children; University of Toronto","funders":"Orionin Tutkimussäätiö; Suomen Kulttuurirahasto; Academy of Finland","keywords":"LRP5; Wnt signaling pathway; Osteoporosis; Missense mutation; Endocrinology; Mutation; Internal medicine; Osteogenesis imperfecta; Biology; Genetics; Medicine; Gene; Pathology","authors":[{"name":"Johanna Korvala","is_ca":false},{"name":"Harald Jüppner","is_ca":false},{"name":"Outi Mäkitie","is_ca":false},{"name":"Etienne Sochett","is_ca":true},{"name":"Dirk Schnabel","is_ca":false},{"name":"Stefano Mora","is_ca":false},{"name":"Cynthia F. Bartels","is_ca":false},{"name":"Matthew L. Warman","is_ca":false},{"name":"D J Deraska","is_ca":false},{"name":"William G. Cole","is_ca":true},{"name":"Heini Hartikka","is_ca":false},{"name":"Leena Ala‐Kokko","is_ca":false},{"name":"Minna Männikkö","is_ca":false}],"retraction":null,"screen_n_in":null,"score":{"opus":0.02576876161115273,"gpt":0.3303399766768738,"spread":0.304571215065721,"validation_status":"score_only:v0-immature-baseline"},"prediction":{"model_version":"metacan-v3-hybrid-931329e0061c","candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0001269509,0.00098548,0.0004465047,0.0004552562,0.0002637015,0.00021145,0.0003324093,0.0006816696,0.003346905],"category_scores_gemma":[0.0004530529,0.0001780859,0.0004603654,0.0003427299,0.0005299119,0.00009262299,0.0003241081,0.0003813001,0.0004748303],"about_ca_system_candidate":false,"about_ca_system_consensus":false,"about_ca_system_score_codex":0.0003069238,"about_ca_system_score_gemma":0.0002251826,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_topic_score_codex":0.001058198,"about_ca_topic_score_gemma":0.001398062,"domain_scores_codex":[0.9997289,0.00002445333,0.00003135799,0.00008387946,0.00008339133,0.00004797903],"domain_scores_gemma":[0.9997243,0.00008042805,0.000115664,0.000011797,0.00001637642,0.00005143352],"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":[0.001336692,0.0002537064,0.1470464,0.0005429296,0.0003585797,0.2060927,0.0006884313,0.0005186318,0.6187397,0.0006031325,0.0008795392,0.0229396],"study_design_scores_gemma":[0.0002068528,0.0008464408,0.4903169,0.000112698,0.0004930143,0.3582385,0.000380666,0.001639345,0.1410662,0.0003168934,0.006345909,0.00003649599],"study_design_candidate":"observational","study_design_consensus":null,"genre_codex":"empirical","genre_gemma":"empirical","genre_scores_codex":[0.9958692,0.0009723559,0.001654273,0.00007225939,0.00001878017,0.00002599612,0.0004204882,0.00006206597,0.0009044539],"genre_scores_gemma":[0.998136,0.000269945,0.0009480771,0.00004205574,0.00001324426,0.00001195928,0.0001996383,0.00001149127,0.0003674944],"genre_candidate":"empirical","genre_consensus":"empirical","teacher_disagreement_score":0.003346905,"threshold_uncertainty_score":0.01119643,"prediction_status":"machine_predicted_unvalidated"},"labels":[],"label_agreement":null},{"id":"W2158992345","doi":"10.1186/s12881-014-0139-9","title":"Mutations in NFKB2and potential genetic heterogeneity in patients with DAVID syndrome, having variable endocrine and immune deficiencies","year":2014,"lang":"en","type":"article","venue":"BMC Medical Genetics","topic":"NF-κB Signaling Pathways","field":"Biochemistry, Genetics and Molecular Biology","cited_by":93,"is_retracted":false,"has_abstract":true,"routes":{"ca_aff":true,"ca_fund":true,"ca_venue":false,"about_ca":false},"ca_institutions":"McGill University; McGill Genome Centre; Centre Hospitalier Universitaire Sainte-Justine; Université de Montréal; Montreal Clinical Research Institute","funders":"Genome British Columbia; Canadian Institutes of Health Research; Genome Canada; Ontario Genomics; Ontario Genomics Institute; Government of Canada; McGill University","keywords":"Sanger sequencing; Biology; Exome sequencing; Genetics; Proband; Mutation; Common variable immunodeficiency; Hypopituitarism; Gene; Endocrinology","authors":[{"name":"Thierry Brue","is_ca":false},{"name":"Marie-Hélène Quentien","is_ca":false},{"name":"Konstantin Khetchoumian","is_ca":true},{"name":"Marco Bensa","is_ca":false},{"name":"José‐Mario Capo‐Chichi","is_ca":true},{"name":"Brigitte Delemer","is_ca":false},{"name":"Aurélio Balsalobre","is_ca":true},{"name":"Christina Nassif","is_ca":true},{"name":"Dimitrios T. Papadimitriou","is_ca":false},{"name":"Anne Pagnier","is_ca":false},{"name":"Caroline Hasselmann","is_ca":true},{"name":"Lysanne Patry","is_ca":true},{"name":"Jeremy Schwartzentruber","is_ca":true},{"name":"Pierre‐François Souchon","is_ca":false},{"name":"Shinobu Takayasu","is_ca":true},{"name":"A Enjalbert","is_ca":false},{"name":"Guy Van Vliet","is_ca":true},{"name":"Jacek Majewski","is_ca":true},{"name":"Jacques Drouin","is_ca":true},{"name":"Mark E. Samuels","is_ca":true}],"retraction":null,"screen_n_in":null,"score":{"opus":0.005527591922303344,"gpt":0.2108944713686755,"spread":0.2053668794463721,"validation_status":"score_only:v0-immature-baseline"},"prediction":{"model_version":"metacan-v3-hybrid-931329e0061c","candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0002014656,0.001078655,0.0003453337,0.001382864,0.0007156279,0.0005085514,0.0004365974,0.000741667,0.002240212],"category_scores_gemma":[0.001039043,0.0002484546,0.0002494462,0.0009245868,0.0005833015,0.0002833917,0.0005537609,0.0002982916,0.0002465954],"about_ca_system_candidate":false,"about_ca_system_consensus":false,"about_ca_system_score_codex":0.0003787267,"about_ca_system_score_gemma":0.0002739741,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_topic_score_codex":0.001226981,"about_ca_topic_score_gemma":0.001720419,"domain_scores_codex":[0.9997469,0.00001845216,0.00003362005,0.00009038318,0.00005306486,0.00005768238],"domain_scores_gemma":[0.9996228,0.000117963,0.00009426673,0.00002046453,0.00003416874,0.0001102995],"domain_codex":null,"domain_gemma":null,"domain_candidate":null,"domain_consensus":null,"study_design_codex":"observational","study_design_gemma":"observational","study_design_scores_codex":[0.0007280711,0.0001330256,0.6225992,0.0001194376,0.00009586666,0.2965989,0.00175978,0.0005081656,0.06449932,0.0008425697,0.0006655258,0.01145024],"study_design_scores_gemma":[0.0001048051,0.0002637384,0.3618509,0.00005126347,0.0001330267,0.6258081,0.0009095428,0.0007881724,0.006961749,0.0006042667,0.002487768,0.00003668739],"study_design_candidate":"observational","study_design_consensus":"observational","genre_codex":"empirical","genre_gemma":"empirical","genre_scores_codex":[0.9989906,0.0001665131,0.0001478321,0.0000265877,0.000003068711,0.000007714488,0.0001034627,0.000008593027,0.0005456181],"genre_scores_gemma":[0.9994357,0.00006372957,0.0002163476,0.00001526592,0.000006778322,0.000004672483,0.0001221461,0.000004500049,0.0001307663],"genre_candidate":"empirical","genre_consensus":"empirical","teacher_disagreement_score":0.002240212,"threshold_uncertainty_score":0.007494271,"prediction_status":"machine_predicted_unvalidated"},"labels":[],"label_agreement":null},{"id":"W2155723834","doi":"10.1186/1471-2350-14-15","title":"A comprehensive investigation of variants in genes encoding adiponectin (ADIPOQ) and its receptors (ADIPOR1/R2), and their association with serum adiponectin, type 2 diabetes, insulin resistance and the metabolic syndrome","year":2013,"lang":"en","type":"article","venue":"BMC Medical Genetics","topic":"Adipokines, Inflammation, and Metabolic Diseases","field":"Medicine","cited_by":91,"is_retracted":false,"has_abstract":true,"routes":{"ca_aff":true,"ca_fund":false,"ca_venue":false,"about_ca":false},"ca_institutions":"Ontario Institute for Cancer Research","funders":"National Health and Medical Research Council; Medical Research Council","keywords":"Adiponectin; Insulin resistance; Type 2 diabetes; Single-nucleotide polymorphism; Internal medicine; Metabolic syndrome; Endocrinology; Population; Adiponectin receptor 1; Haplotype; Medicine; Biology; Diabetes mellitus; Genotype; Obesity; Genetics; Gene","authors":[{"name":"Kirsten E. Peters","is_ca":false},{"name":"John Beilby","is_ca":false},{"name":"Gemma Cadby","is_ca":false},{"name":"Nicole M. Warrington","is_ca":false},{"name":"David Bruce","is_ca":false},{"name":"Wendy A. Davis","is_ca":false},{"name":"Timothy M. E. Davis","is_ca":false},{"name":"Steven Wiltshire","is_ca":false},{"name":"Matthew Knuiman","is_ca":false},{"name":"B. McQuillan","is_ca":false},{"name":"Lyle J. Palmer","is_ca":true},{"name":"Peter L. Thompson","is_ca":false},{"name":"Joseph Hung","is_ca":false}],"retraction":null,"screen_n_in":null,"score":{"opus":0.0153376748258415,"gpt":0.2264655757914373,"spread":0.2111279009655958,"validation_status":"score_only:v0-immature-baseline"},"prediction":{"model_version":"metacan-v3-hybrid-931329e0061c","candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.003467423,0.000971225,0.001497979,0.001886855,0.0004197217,0.0007131898,0.0005056399,0.0005669938,0.0009362315],"category_scores_gemma":[0.002710972,0.000412804,0.003153299,0.004418129,0.0003085345,0.00028373,0.0007112571,0.0004562294,0.0001146814],"about_ca_system_candidate":false,"about_ca_system_consensus":false,"about_ca_system_score_codex":0.0004416058,"about_ca_system_score_gemma":0.001337953,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_topic_score_codex":0.006231784,"about_ca_topic_score_gemma":0.01119662,"domain_scores_codex":[0.9986034,0.0004842444,0.0001683888,0.0004519107,0.000226985,0.00006494441],"domain_scores_gemma":[0.9984067,0.0006771447,0.0003829635,0.0002077806,0.0002163374,0.0001089671],"domain_codex":null,"domain_gemma":null,"domain_candidate":null,"domain_consensus":null,"study_design_codex":"observational","study_design_gemma":"observational","study_design_scores_codex":[0.003470491,0.0002484785,0.7576673,0.008141224,0.114569,0.001531147,0.0005250397,0.004458209,0.02490529,0.0005651865,0.002353132,0.0815655],"study_design_scores_gemma":[0.0005867431,0.001087669,0.9053215,0.0008034065,0.07928858,0.001277377,0.0001740487,0.001768031,0.002335574,0.0006610312,0.006645663,0.00005031765],"study_design_candidate":"observational","study_design_consensus":"observational","genre_codex":"empirical","genre_gemma":"empirical","genre_scores_codex":[0.8270156,0.1608324,0.006012158,0.0009163027,0.0001408761,0.0001368834,0.003822158,0.00009639016,0.001027171],"genre_scores_gemma":[0.9681423,0.02523393,0.003570986,0.0002800175,0.00008391998,0.00009255687,0.002011854,0.00001593659,0.0005685818],"genre_candidate":"empirical","genre_consensus":"empirical","teacher_disagreement_score":0.006231784,"threshold_uncertainty_score":0.01833773,"prediction_status":"machine_predicted_unvalidated"},"labels":[],"label_agreement":null},{"id":"W2024863238","doi":"10.1186/1471-2350-10-108","title":"Association of APOEpolymorphism with chronic kidney disease in a nationally representative sample: a Third National Health and Nutrition Examination Survey (NHANES III) Genetic Study","year":2009,"lang":"en","type":"article","venue":"BMC Medical Genetics","topic":"Chronic Kidney Disease and Diabetes","field":"Medicine","cited_by":85,"is_retracted":false,"has_abstract":true,"routes":{"ca_aff":true,"ca_fund":false,"ca_venue":false,"about_ca":false},"ca_institutions":"SickKids Foundation; Hospital for Sick Children; University of Toronto; University Health Network","funders":"National Institute of Diabetes and Digestive and Kidney Diseases; National Heart, Lung, and Blood Institute","keywords":"National Health and Nutrition Examination Survey; Renal function; Medicine; Kidney disease; Odds ratio; Confidence interval; Internal medicine; Apolipoprotein E; Allele; Cohort; Population; Endocrinology; Disease; Biology; Genetics; Environmental health","authors":[{"name":"Audrey Y. Chu","is_ca":false},{"name":"Rulan S. Parekh","is_ca":true},{"name":"Brad C. Astor","is_ca":false},{"name":"Josef Coresh","is_ca":false},{"name":"Yvette Berthier‐Schaad","is_ca":false},{"name":"Michael W. Smith","is_ca":false},{"name":"Alan R. Shuldiner","is_ca":false},{"name":"Wen Hong Linda Kao","is_ca":false}],"retraction":null,"screen_n_in":null,"score":{"opus":0.02442267946644579,"gpt":0.3189458141178049,"spread":0.2945231346513592,"validation_status":"score_only:v0-immature-baseline"},"prediction":{"model_version":"metacan-v3-hybrid-931329e0061c","candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.001230401,0.0002282826,0.0004227292,0.00053859,0.0004244761,0.0005177546,0.0003222125,0.0005201349,0.0006970133],"category_scores_gemma":[0.001829011,0.0003314028,0.0004858613,0.0007550541,0.0001949722,0.0002428727,0.0003186505,0.0005059121,0.0002085358],"about_ca_system_candidate":false,"about_ca_system_consensus":false,"about_ca_system_score_codex":0.0002428989,"about_ca_system_score_gemma":0.0003290557,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_topic_score_codex":0.01035954,"about_ca_topic_score_gemma":0.01019646,"domain_scores_codex":[0.9992903,0.0002426871,0.00007872588,0.0001865404,0.0001338469,0.00006774218],"domain_scores_gemma":[0.9987891,0.0001744481,0.0004422036,0.0001913547,0.0001853851,0.0002174881],"domain_codex":null,"domain_gemma":null,"domain_candidate":null,"domain_consensus":null,"study_design_codex":"observational","study_design_gemma":"observational","study_design_scores_codex":[0.0000508339,0.00002594879,0.9994105,0.000002511015,0.00007772407,0.00002580009,0.00002843868,0.000009122182,0.0001548141,0.000005109595,0.00003754414,0.0001716414],"study_design_scores_gemma":[0.000004779679,0.00003783482,0.999668,0.00000179251,0.00002383149,0.00008964221,0.00004622961,0.00005689344,0.00002283025,0.000006026446,0.00004101239,0.000001101171],"study_design_candidate":"observational","study_design_consensus":"observational","genre_codex":"empirical","genre_gemma":"empirical","genre_scores_codex":[0.9992306,0.00006556508,0.00009410133,0.00002171395,0.000003504066,0.000009089601,0.0004159835,0.000002411557,0.0001571527],"genre_scores_gemma":[0.9988973,0.00005433888,0.0001599981,0.00004464418,0.000006419153,0.00001677486,0.000688962,0.000002415159,0.0001292474],"genre_candidate":"empirical","genre_consensus":"empirical","teacher_disagreement_score":0.01035954,"threshold_uncertainty_score":0.02059847,"prediction_status":"machine_predicted_unvalidated"},"labels":[],"label_agreement":null},{"id":"W1482289836","doi":"10.1186/1471-2350-7-60","title":"Familial deletion 18p syndrome: case report","year":2006,"lang":"en","type":"article","venue":"BMC Medical Genetics","topic":"Genomic variations and chromosomal abnormalities","field":"Biochemistry, Genetics and Molecular Biology","cited_by":85,"is_retracted":false,"has_abstract":true,"routes":{"ca_aff":true,"ca_fund":false,"ca_venue":false,"about_ca":false},"ca_institutions":"Université de Montréal","funders":"","keywords":"Proband; Short stature; Genetic counseling; Psychology; Pediatrics; Cognition; Genetics; Chromosomal Deletion; Chromosome; Medicine; Psychiatry; Biology; Mutation","authors":[{"name":"Bruno Maranda","is_ca":true},{"name":"Nicole Lemieux","is_ca":true},{"name":"Emmanuelle Lemyre","is_ca":true}],"retraction":null,"screen_n_in":null,"score":{"opus":0.008387568449679644,"gpt":0.2320938735468008,"spread":0.2237063050971212,"validation_status":"score_only:v0-immature-baseline"},"prediction":{"model_version":"metacan-v3-hybrid-931329e0061c","candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00038712,0.002709019,0.001226551,0.0021863,0.002037523,0.001034325,0.00125916,0.003866529,0.002968763],"category_scores_gemma":[0.00224529,0.001166448,0.0008557755,0.001905683,0.001914903,0.001008205,0.002002888,0.002020704,0.001333937],"about_ca_system_candidate":false,"about_ca_system_consensus":false,"about_ca_system_score_codex":0.000603481,"about_ca_system_score_gemma":0.0006353635,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_topic_score_codex":0.00146461,"about_ca_topic_score_gemma":0.001346527,"domain_scores_codex":[0.999376,0.0000842426,0.00007163008,0.0001760339,0.00009705746,0.0001950929],"domain_scores_gemma":[0.9987233,0.0003611791,0.000349534,0.000121342,0.00007832619,0.0003662621],"domain_codex":null,"domain_gemma":null,"domain_candidate":null,"domain_consensus":null,"study_design_codex":"case_report","study_design_gemma":"case_report","study_design_scores_codex":[0.00001707649,0.00001717367,0.003680406,0.00002818597,0.00001273503,0.9940273,0.0001361429,0.0000465732,0.0005535615,0.0000644666,0.0003246911,0.001091744],"study_design_scores_gemma":[0.000006649591,0.00001939024,0.001325059,0.000005016379,0.000009286508,0.9980779,0.00003577205,0.00003432368,0.0001155197,0.00004009968,0.0003275221,0.000003441541],"study_design_candidate":"case_report","study_design_consensus":"case_report","genre_codex":"empirical","genre_gemma":"empirical","genre_scores_codex":[0.9758671,0.009773362,0.003692729,0.001882065,0.0003159973,0.0001626926,0.0003859619,0.0003840242,0.007536148],"genre_scores_gemma":[0.9941544,0.002375075,0.001207671,0.0003756544,0.0003918222,0.00004028139,0.0001651954,0.00002687155,0.001263117],"genre_candidate":"empirical","genre_consensus":"empirical","teacher_disagreement_score":0.003866529,"threshold_uncertainty_score":0.009931505,"prediction_status":"machine_predicted_unvalidated"},"labels":[],"label_agreement":null},{"id":"W1923182887","doi":"10.1186/1471-2350-7-71","title":"Genome-wide significance for a modifier of age at neurological onset in Huntington's Disease at 6q23-24: the HD MAPS study","year":2006,"lang":"en","type":"article","venue":"BMC Medical Genetics","topic":"Genetic Neurodegenerative Diseases","field":"Neuroscience","cited_by":79,"is_retracted":false,"has_abstract":true,"routes":{"ca_aff":true,"ca_fund":true,"ca_venue":false,"about_ca":false},"ca_institutions":"University of Calgary; University of British Columbia","funders":"National Center for Research Resources; National Institute of Neurological Disorders and Stroke; Canadian Institutes of Health Research; National Institutes of Health","keywords":"Pedigree chart; Biology; Genetics; Genome Scan; Quantitative trait locus; Linkage (software); Genetic linkage; Microsatellite; Human genetics; Allele; Gene","authors":[{"name":"Jian‐Liang Li","is_ca":false},{"name":"Michael R. Hayden","is_ca":true},{"name":"Simon C. Warby","is_ca":true},{"name":"Alexandra Dürr","is_ca":false},{"name":"Patrick J. Morrison","is_ca":false},{"name":"Martha Nance","is_ca":false},{"name":"Christopher A. Ross","is_ca":false},{"name":"Russell L. Margolis","is_ca":false},{"name":"Adam Rosenblatt","is_ca":false},{"name":"Ferdinando Squitieri","is_ca":false},{"name":"Luigi Frati","is_ca":false},{"name":"Estrella Gómez‐Tortosa","is_ca":false},{"name":"Carmen Ayuso","is_ca":false},{"name":"Oksana Suchowersky","is_ca":true},{"name":"Mary Lou Klimek","is_ca":true},{"name":"Ronald J. Trent","is_ca":false},{"name":"Elizabeth McCusker","is_ca":false},{"name":"Andrea Novelletto","is_ca":false},{"name":"Marina Frontali","is_ca":false},{"name":"Jane S. Paulsen","is_ca":false},{"name":"Randi Jones","is_ca":false},{"name":"Tetsuo Ashizawa","is_ca":false},{"name":"Alice Lazzarini","is_ca":false},{"name":"Vanessa C. Wheeler","is_ca":false},{"name":"Ranjana Prakash","is_ca":false},{"name":"Gang Xu","is_ca":false},{"name":"Luc Djoussé","is_ca":false},{"name":"Jayalakshmi Srinidhi Mysore","is_ca":false},{"name":"Tammy Gillis","is_ca":false},{"name":"Michael Hakky","is_ca":false},{"name":"L. Adrienne Cupples","is_ca":false},{"name":"Marie Saint‐Hilaire","is_ca":false},{"name":"J. Jang-Ho","is_ca":false},{"name":"Steven M. Hersch","is_ca":false},{"name":"John B. Penney","is_ca":false},{"name":"Madaline B. Harrison","is_ca":false},{"name":"Susan Perlman","is_ca":false},{"name":"Andrea Zanko","is_ca":false},{"name":"Ruth K. Abramson","is_ca":false},{"name":"Anthony J. Lechich","is_ca":false},{"name":"Ayana Duckett","is_ca":false},{"name":"Karen Marder","is_ca":false},{"name":"P. Michael Conneally","is_ca":false},{"name":"James F. Gusella","is_ca":false},{"name":"Marcy E. MacDonald","is_ca":false},{"name":"Richard H. Myers","is_ca":false}],"retraction":null,"screen_n_in":null,"score":{"opus":0.04916127282059388,"gpt":0.2837990846260579,"spread":0.234637811805464,"validation_status":"score_only:v0-immature-baseline"},"prediction":{"model_version":"metacan-v3-hybrid-931329e0061c","candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.001236815,0.0006329067,0.0005379828,0.000999089,0.0006752039,0.0006118821,0.0005907484,0.0007667497,0.002401864],"category_scores_gemma":[0.002769771,0.0002591728,0.0009309336,0.0009112869,0.0003339903,0.0001855834,0.0005796615,0.0006648134,0.0001464254],"about_ca_system_candidate":false,"about_ca_system_consensus":false,"about_ca_system_score_codex":0.0002410753,"about_ca_system_score_gemma":0.0002663669,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_topic_score_codex":0.007333341,"about_ca_topic_score_gemma":0.004928825,"domain_scores_codex":[0.9992623,0.0002598065,0.00003193894,0.0002911266,0.0000958464,0.00005893555],"domain_scores_gemma":[0.9985536,0.0005193939,0.0003540219,0.0001657431,0.000112362,0.0002949131],"domain_codex":null,"domain_gemma":null,"domain_candidate":null,"domain_consensus":null,"study_design_codex":"observational","study_design_gemma":"observational","study_design_scores_codex":[0.001786211,0.00008058197,0.9796306,0.00004039619,0.001450874,0.001171934,0.0004857935,0.0002425628,0.008791498,0.00009630327,0.0003801103,0.005843204],"study_design_scores_gemma":[0.0000348318,0.0001023644,0.9984586,0.000003644707,0.0002746344,0.0003405673,0.00005429736,0.0001977263,0.0002670393,0.00003936441,0.0002225109,0.000004464515],"study_design_candidate":"observational","study_design_consensus":"observational","genre_codex":"empirical","genre_gemma":"empirical","genre_scores_codex":[0.9986839,0.000315817,0.0003709169,0.00005652036,0.00000813262,0.000008157671,0.0003806492,0.00001479023,0.0001611409],"genre_scores_gemma":[0.9989871,0.00007862667,0.000347403,0.00001805208,0.00001797754,0.000008607564,0.0002905908,0.000007239391,0.000244317],"genre_candidate":"empirical","genre_consensus":"empirical","teacher_disagreement_score":0.007333341,"threshold_uncertainty_score":0.01458132,"prediction_status":"machine_predicted_unvalidated"},"labels":[],"label_agreement":null},{"id":"W2081704195","doi":"10.1186/1471-2350-12-102","title":"Combined analysis of three genome-wide association studies on vWF and FVIII plasma levels","year":2011,"lang":"en","type":"review","venue":"BMC Medical Genetics","topic":"Blood Coagulation and Thrombosis Mechanisms","field":"Medicine","cited_by":74,"is_retracted":false,"has_abstract":true,"routes":{"ca_aff":true,"ca_fund":true,"ca_venue":false,"about_ca":false},"ca_institutions":"Ottawa Hospital; Public Health Ontario; University of Toronto","funders":"Canadian Institutes of Health Research; Fondation pour la Recherche Médicale; Institut National de la Santé et de la Recherche Médicale; Canada Research Chairs; Heart and Stroke Foundation of Canada","keywords":"Single-nucleotide polymorphism; Von Willebrand factor; Genome-wide association study; Genetic association; SNP; Genetics; Biology; Heritability; Von Willebrand disease; Meta-analysis; Gene; Internal medicine; Medicine; Bioinformatics; Immunology; Genotype; Platelet","authors":[{"name":"Guillemette Antoni","is_ca":false},{"name":"Tiphaine Oudot‐Mellakh","is_ca":false},{"name":"Apostolos Dimitromanolakis","is_ca":true},{"name":"Marine Germain","is_ca":false},{"name":"William Cohen","is_ca":false},{"name":"Philip Wells","is_ca":true},{"name":"Mark Lathrop","is_ca":false},{"name":"France Gagnon","is_ca":true},{"name":"Pierre‐Emmanuel Morange","is_ca":false},{"name":"David‐Alexandre Trégouët","is_ca":false}],"retraction":null,"screen_n_in":null,"score":{"opus":0.2012398512231197,"gpt":0.3757346687649928,"spread":0.1744948175418731,"validation_status":"score_only:v0-immature-baseline"},"prediction":{"model_version":"metacan-v3-hybrid-931329e0061c","candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00907662,0.002473783,0.005234959,0.004743245,0.001007688,0.002226341,0.00114302,0.00179397,0.003099978],"category_scores_gemma":[0.01165516,0.0009509746,0.01847217,0.007403298,0.0004142302,0.0005673332,0.001444614,0.001317749,0.0003678337],"about_ca_system_candidate":false,"about_ca_system_consensus":false,"about_ca_system_score_codex":0.0005046178,"about_ca_system_score_gemma":0.001260246,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_topic_score_codex":0.004769094,"about_ca_topic_score_gemma":0.0064819,"domain_scores_codex":[0.9919308,0.003737744,0.001080394,0.00211905,0.0007645491,0.0003674453],"domain_scores_gemma":[0.9885452,0.007692463,0.0009847765,0.001332592,0.001003701,0.0004412321],"domain_codex":null,"domain_gemma":null,"domain_candidate":null,"domain_consensus":null,"study_design_codex":"observational","study_design_gemma":"meta_analysis","study_design_scores_codex":[0.009685331,0.0001231092,0.5656251,0.002838559,0.3938113,0.001452156,0.0001557043,0.002061246,0.007287726,0.000175875,0.0008316627,0.01595229],"study_design_scores_gemma":[0.001183108,0.001164293,0.3931716,0.0003219538,0.5951006,0.001253128,0.0001665464,0.002580565,0.001936423,0.0006597344,0.002388412,0.00007360447],"study_design_candidate":"meta_analysis","study_design_consensus":null,"genre_codex":"empirical","genre_gemma":"review","genre_scores_codex":[0.8677487,0.1052703,0.01391957,0.0008122925,0.0004601417,0.0002894934,0.009598041,0.0003034357,0.001597966],"genre_scores_gemma":[0.9821401,0.006949838,0.005884309,0.00019287,0.0001206231,0.0002126691,0.004051519,0.00005908435,0.0003890025],"genre_candidate":"review","genre_consensus":null,"teacher_disagreement_score":0.00907662,"threshold_uncertainty_score":0.04800236,"prediction_status":"machine_predicted_unvalidated"},"labels":[],"label_agreement":null},{"id":"W1529054707","doi":"10.1186/1471-2350-5-4","title":"Amyloidosis in familial Mediterranean fever patients: correlation with MEFV genotype and SAA1 and MICA polymorphisms effects","year":2004,"lang":"en","type":"article","venue":"BMC Medical Genetics","topic":"Inflammasome and immune disorders","field":"Biochemistry, Genetics and Molecular Biology","cited_by":69,"is_retracted":false,"has_abstract":true,"routes":{"ca_aff":false,"ca_fund":true,"ca_venue":false,"about_ca":false},"ca_institutions":"","funders":"Saint Joseph University; Agence Universitaire de la Francophonie","keywords":"Familial Mediterranean fever; MEFV; Amyloidosis; AA amyloidosis; Allele; Genotype; Immunology; Gastroenterology; Pathology; Medicine; Internal medicine; Biology; Disease; Gene mutation; Genetics; Mutation; Gene","authors":[{"name":"Myrna Medlej‐Hashim","is_ca":false},{"name":"Valérie Delague","is_ca":false},{"name":"Éliane Chouery","is_ca":false},{"name":"Nabiha Salem","is_ca":false},{"name":"M. O. Rawashdeh","is_ca":false},{"name":"Jacques Loiselet","is_ca":false},{"name":"André Mégarbané","is_ca":false}],"retraction":null,"screen_n_in":null,"score":{"opus":0.003889643538659336,"gpt":0.2002929754923656,"spread":0.1964033319537062,"validation_status":"score_only:v0-immature-baseline"},"prediction":{"model_version":"metacan-v3-hybrid-931329e0061c","candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0003375532,0.0003767805,0.0003151432,0.0007280372,0.0004805537,0.0003129501,0.0001363872,0.000489525,0.001670939],"category_scores_gemma":[0.001934289,0.000210316,0.0002342948,0.0004548043,0.0002954674,0.0002165511,0.0001839362,0.0003616741,0.0001600894],"about_ca_system_candidate":false,"about_ca_system_consensus":false,"about_ca_system_score_codex":0.0001198008,"about_ca_system_score_gemma":0.00009559879,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_topic_score_codex":0.0004942057,"about_ca_topic_score_gemma":0.0004653213,"domain_scores_codex":[0.9996865,0.000108614,0.00003383764,0.00006520822,0.0000541527,0.00005175716],"domain_scores_gemma":[0.9989415,0.0003261936,0.0004047916,0.00004098607,0.00008011064,0.0002063852],"domain_codex":null,"domain_gemma":null,"domain_candidate":null,"domain_consensus":null,"study_design_codex":"observational","study_design_gemma":"observational","study_design_scores_codex":[0.0002574461,0.00004217455,0.9958856,0.000008910306,0.00004240965,0.0009381226,0.0001075227,0.00003326792,0.001204698,0.00001643668,0.00005923327,0.001404199],"study_design_scores_gemma":[0.00001675985,0.0002833944,0.9916963,0.000007257351,0.00003813985,0.007275668,0.0001342333,0.0001535978,0.0001916577,0.00005100969,0.0001474987,0.000004484277],"study_design_candidate":"observational","study_design_consensus":"observational","genre_codex":"empirical","genre_gemma":"empirical","genre_scores_codex":[0.9995657,0.0001786228,0.00004236077,0.00001696611,0.00000330994,0.00000259851,0.0000177097,0.000001694791,0.000171079],"genre_scores_gemma":[0.999851,0.00003588875,0.00003466964,0.000008412857,0.000009151442,0.000002146028,0.00002256066,5.778039e-7,0.00003551809],"genre_candidate":"empirical","genre_consensus":"empirical","teacher_disagreement_score":0.001670939,"threshold_uncertainty_score":0.005589783,"prediction_status":"machine_predicted_unvalidated"},"labels":[],"label_agreement":null},{"id":"W2118639499","doi":"10.1186/1471-2350-7-3","title":"Peroxisomal proliferator activated receptor-γ deficiency in a Canadian kindred with familial partial lipodystrophy type 3 (FPLD3)","year":2006,"lang":"en","type":"article","venue":"BMC Medical Genetics","topic":"Peroxisome Proliferator-Activated Receptors","field":"Biochemistry, Genetics and Molecular Biology","cited_by":67,"is_retracted":false,"has_abstract":true,"routes":{"ca_aff":true,"ca_fund":true,"ca_venue":false,"about_ca":true},"ca_institutions":"Western University; Robarts Clinical Trials; University of Calgary; University of Alberta","funders":"Canadian Institutes of Health Research; Fondation pour la Recherche Médicale; Genome Canada; Heart and Stroke Foundation of Canada","keywords":"Haploinsufficiency; Endocrinology; Internal medicine; Peroxisome proliferator-activated receptor gamma; Biology; Genetics; Receptor; Peroxisome proliferator-activated receptor; Phenotype; Medicine; Gene","authors":[{"name":"Gordon A. Francis","is_ca":true},{"name":"Gang Li","is_ca":false},{"name":"Robin Casey","is_ca":true},{"name":"Jian Wang","is_ca":true},{"name":"Henian Cao","is_ca":true},{"name":"Todd Leff","is_ca":false},{"name":"Robert A. Hegele","is_ca":true}],"retraction":null,"screen_n_in":null,"score":{"opus":0.007669925116398854,"gpt":0.2276779043600994,"spread":0.2200079792437005,"validation_status":"score_only:v0-immature-baseline"},"prediction":{"model_version":"metacan-v3-hybrid-931329e0061c","candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0001491242,0.001547394,0.0003942132,0.001368315,0.003024939,0.0004318523,0.0006812214,0.001074637,0.004111735],"category_scores_gemma":[0.0006690657,0.0003885484,0.0005989713,0.001856381,0.001231506,0.0001836215,0.0007461008,0.0007574781,0.0004054381],"about_ca_system_candidate":false,"about_ca_system_consensus":false,"about_ca_system_score_codex":0.004550516,"about_ca_system_score_gemma":0.00524791,"about_ca_topic_candidate":true,"about_ca_topic_consensus":true,"about_ca_topic_score_codex":0.5828547,"about_ca_topic_score_gemma":0.6669549,"domain_scores_codex":[0.999761,0.00001108251,0.00001374728,0.0000467254,0.00009448003,0.00007294059],"domain_scores_gemma":[0.999757,0.00003858297,0.00004232583,0.000009781535,0.00005470932,0.00009767511],"domain_codex":null,"domain_gemma":null,"domain_candidate":null,"domain_consensus":null,"study_design_codex":"case_report","study_design_gemma":"observational","study_design_scores_codex":[0.0008486629,0.0001245547,0.06609414,0.0003075392,0.0001587752,0.8439169,0.003264635,0.0006751511,0.05354001,0.002253766,0.005316467,0.02349937],"study_design_scores_gemma":[0.0001027256,0.0001948783,0.1723885,0.00009335261,0.0002069209,0.8059474,0.001389353,0.0009536152,0.005725698,0.0005511958,0.0123171,0.0001293731],"study_design_candidate":"observational","study_design_consensus":null,"genre_codex":"empirical","genre_gemma":"empirical","genre_scores_codex":[0.9858191,0.001034812,0.001235688,0.00111183,0.00007784396,0.00009249111,0.001198684,0.0001037888,0.009325691],"genre_scores_gemma":[0.9920643,0.0007605139,0.002080403,0.0002841762,0.0000244599,0.00001688964,0.0004039613,0.00004045908,0.004324818],"genre_candidate":"empirical","genre_consensus":"empirical","teacher_disagreement_score":0.4171453,"threshold_uncertainty_score":0.839204,"prediction_status":"machine_predicted_unvalidated"},"labels":[],"label_agreement":null},{"id":"W1995716751","doi":"10.1186/1471-2350-12-95","title":"Genetic polymorphisms of innate immunity-related inflammatory pathways and their association with factors related to type 2 diabetes","year":2011,"lang":"en","type":"article","venue":"BMC Medical Genetics","topic":"Adipokines, Inflammation, and Metabolic Diseases","field":"Medicine","cited_by":67,"is_retracted":false,"has_abstract":true,"routes":{"ca_aff":true,"ca_fund":true,"ca_venue":false,"about_ca":false},"ca_institutions":"McGill University; Public Health Ontario; University of Toronto; Public Health Agency of Canada","funders":"Biotechnology and Biological Sciences Research Council; Fonds de Recherche du Québec - Santé; Versus Arthritis; Directorate for Biological Sciences; National Institute for Health and Care Research; Jewish General Hospital; Public Health Agency; European Commission; King's College London; Canadian Institutes of Health Research; Public Health Agency of Canada; Wellcome Trust","keywords":"Human genetics; Biology; Innate immune system; Genetics; Immunology; Type 1 diabetes; Immunity; Genetic association; Diabetes mellitus; Computational biology; Genotype; Gene; Single-nucleotide polymorphism; Immune system","authors":[{"name":"Paul Arora","is_ca":true},{"name":"Bibiana García‐Bailo","is_ca":true},{"name":"Zari Dastani","is_ca":true},{"name":"Darren R. Brenner","is_ca":true},{"name":"André Villegas","is_ca":true},{"name":"Suneil Malik","is_ca":true},{"name":"Timothy D. Spector","is_ca":false},{"name":"Brent Richards","is_ca":true},{"name":"Ahmed El‐Sohemy","is_ca":true},{"name":"Mohamed A. Karmali","is_ca":true},{"name":"Alaa Badawi","is_ca":true}],"retraction":null,"screen_n_in":null,"score":{"opus":0.01743726217128133,"gpt":0.2203372403260776,"spread":0.2028999781547963,"validation_status":"score_only:v0-immature-baseline"},"prediction":{"model_version":"metacan-v3-hybrid-931329e0061c","candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0007582765,0.0003980501,0.0003324673,0.0006934722,0.0003589965,0.0004581522,0.0002595432,0.0005460107,0.002413988],"category_scores_gemma":[0.002267651,0.0002185698,0.0004556411,0.001133583,0.000295939,0.0001487538,0.0002793995,0.0006363306,0.0001907759],"about_ca_system_candidate":false,"about_ca_system_consensus":false,"about_ca_system_score_codex":0.0001583036,"about_ca_system_score_gemma":0.0001945757,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_topic_score_codex":0.002189636,"about_ca_topic_score_gemma":0.001809847,"domain_scores_codex":[0.999455,0.000197318,0.00006017808,0.0001498982,0.00007503038,0.00006251381],"domain_scores_gemma":[0.9983725,0.0005999049,0.000559751,0.0001095977,0.000128565,0.0002297894],"domain_codex":null,"domain_gemma":null,"domain_candidate":null,"domain_consensus":null,"study_design_codex":"observational","study_design_gemma":"observational","study_design_scores_codex":[0.0005551666,0.00005844433,0.9962275,0.00001518166,0.0002570731,0.0001713733,0.00006146864,0.00006557213,0.001308992,0.00002982771,0.00005211469,0.001197127],"study_design_scores_gemma":[0.0000166534,0.0001115168,0.9986518,0.000009928384,0.0001378186,0.0004905334,0.00004078355,0.0001830721,0.0001883691,0.00005527552,0.0001109139,0.000003213137],"study_design_candidate":"observational","study_design_consensus":"observational","genre_codex":"empirical","genre_gemma":"empirical","genre_scores_codex":[0.9990494,0.0003806643,0.0001317012,0.00003444636,0.000007801418,0.000005326623,0.000173078,0.000002822063,0.0002147572],"genre_scores_gemma":[0.9993234,0.0001258009,0.0002191775,0.00001618491,0.00001162506,0.000007855691,0.0001569343,0.000002216057,0.0001369095],"genre_candidate":"empirical","genre_consensus":"empirical","teacher_disagreement_score":0.002413988,"threshold_uncertainty_score":0.008075595,"prediction_status":"machine_predicted_unvalidated"},"labels":[],"label_agreement":null},{"id":"W1996371870","doi":"10.1186/1471-2350-12-1","title":"HNF1AG319S variant, active cigarette smoking and incident type 2 diabetes in Aboriginal Canadians: a population-based epidemiological study","year":2011,"lang":"en","type":"article","venue":"BMC Medical Genetics","topic":"Pancreatic function and diabetes","field":"Medicine","cited_by":67,"is_retracted":false,"has_abstract":true,"routes":{"ca_aff":true,"ca_fund":true,"ca_venue":false,"about_ca":false},"ca_institutions":"Lunenfeld-Tanenbaum Research Institute; St. Michael's Hospital; Mount Sinai Hospital; Western University; University of Toronto","funders":"Ontario Ministry of Research and Innovation; Genome Canada; Canadian Institutes of Health Research; University of Toronto; Banting and Best Diabetes Centre, University of Toronto; Canadian Diabetes Association","keywords":"Medicine; Type 2 diabetes; HNF1A; Diabetes mellitus; Population; Odds ratio; Internal medicine; Epidemiology; Demography; Endocrinology; Environmental health","authors":[{"name":"Sylvia H. Ley","is_ca":true},{"name":"Robert A. Hegele","is_ca":true},{"name":"Stewart B. Harris","is_ca":true},{"name":"Mary Mamakeesick","is_ca":false},{"name":"Henian Cao","is_ca":true},{"name":"Philip W. Connelly","is_ca":true},{"name":"Joel Gittelsohn","is_ca":false},{"name":"Ravi Retnakaran","is_ca":true},{"name":"Bernard Zinman","is_ca":true},{"name":"Anthony J. Hanley","is_ca":true}],"retraction":null,"screen_n_in":null,"score":{"opus":0.04554427197874367,"gpt":0.3101496753702129,"spread":0.2646054033914693,"validation_status":"score_only:v0-immature-baseline"},"prediction":{"model_version":"metacan-v3-hybrid-931329e0061c","candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.000617013,0.0003934721,0.0004427624,0.0009415178,0.002842419,0.000886129,0.0008130225,0.0007021825,0.001643535],"category_scores_gemma":[0.001052846,0.0003811627,0.0005366793,0.002369125,0.0005599217,0.000242389,0.0003979816,0.0007338704,0.0001969701],"about_ca_system_candidate":false,"about_ca_system_consensus":false,"about_ca_system_score_codex":0.00450602,"about_ca_system_score_gemma":0.005522056,"about_ca_topic_candidate":true,"about_ca_topic_consensus":true,"about_ca_topic_score_codex":0.9288251,"about_ca_topic_score_gemma":0.9211322,"domain_scores_codex":[0.9996183,0.00003356002,0.00001872171,0.00008294312,0.0001483045,0.00009814314],"domain_scores_gemma":[0.9993279,0.00004454912,0.0001244139,0.00003856662,0.0002584673,0.0002061479],"domain_codex":null,"domain_gemma":null,"domain_candidate":null,"domain_consensus":null,"study_design_codex":"observational","study_design_gemma":"observational","study_design_scores_codex":[0.0001087717,0.00004679623,0.9976165,0.00002533273,0.0001151708,0.00009549218,0.0003837393,0.00003250334,0.0001965453,0.00002394923,0.0002955899,0.001059438],"study_design_scores_gemma":[0.00001210498,0.00003221262,0.9990267,0.00001185999,0.00006198425,0.0001099879,0.00034362,0.00008868974,0.00001648486,0.000012861,0.0002779007,0.000005712917],"study_design_candidate":"observational","study_design_consensus":"observational","genre_codex":"empirical","genre_gemma":"empirical","genre_scores_codex":[0.9977177,0.0004749637,0.00005726695,0.0001146572,0.000008789745,0.00002456741,0.000911922,0.000004844946,0.0006852087],"genre_scores_gemma":[0.9984054,0.0003374495,0.0001811337,0.00007230668,0.00001195885,0.0000157811,0.0006386838,0.000002686998,0.0003346263],"genre_candidate":"empirical","genre_consensus":"empirical","teacher_disagreement_score":0.07117486,"threshold_uncertainty_score":0.143188,"prediction_status":"machine_predicted_unvalidated"},"labels":[],"label_agreement":null},{"id":"W2066325911","doi":"10.1186/1471-2350-14-21","title":"Analysis of the contribution of FTO, NPC1, ENPP1, NEGR1, GNPDA2 and MC4Rgenes to obesity in Mexican children","year":2013,"lang":"en","type":"article","venue":"BMC Medical Genetics","topic":"Genetic Associations and Epidemiology","field":"Biochemistry, Genetics and Molecular Biology","cited_by":64,"is_retracted":false,"has_abstract":true,"routes":{"ca_aff":true,"ca_fund":false,"ca_venue":false,"about_ca":false},"ca_institutions":"McMaster University","funders":"Fundación Gonzalo Río Arronte; Fundación IMSS; Instituto Mexicano del Seguro Social; Consejo Nacional de Ciencia y Tecnología","keywords":"Obesity; Single-nucleotide polymorphism; Body mass index; Genome-wide association study; Medicine; Internal medicine; Odds ratio; Endocrinology; Insulin resistance; Biology; Genetics; Genotype; Gene","authors":[{"name":"Aurora Mejía‐Benítez","is_ca":false},{"name":"Miguel Klünder‐Klünder","is_ca":false},{"name":"Loïc Yengo","is_ca":false},{"name":"David Meyre","is_ca":true},{"name":"Esperanza de la Cruz","is_ca":false},{"name":"Elva Pérez‐Luque","is_ca":false},{"name":"Juan Manuel Malacara","is_ca":false},{"name":"Maria Eugenia Garay","is_ca":false},{"name":"Jesús Peralta‐Romero","is_ca":false},{"name":"Samuel Flores‐Huerta","is_ca":false},{"name":"Jaime Garcı́a-Mena","is_ca":false},{"name":"Philippe Froguel","is_ca":false},{"name":"Miguel Cruz","is_ca":false},{"name":"Amélie Bonnefond","is_ca":false}],"retraction":null,"screen_n_in":null,"score":{"opus":0.006941073021086899,"gpt":0.2543017420600345,"spread":0.2473606690389476,"validation_status":"score_only:v0-immature-baseline"},"prediction":{"model_version":"metacan-v3-hybrid-931329e0061c","candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0005532654,0.0004021569,0.0002620968,0.0007102861,0.0003160564,0.0003625709,0.0003146686,0.000280344,0.001418912],"category_scores_gemma":[0.001130683,0.000229519,0.0005533543,0.0006839445,0.00028179,0.0001271708,0.0003899413,0.0003474814,0.0001157548],"about_ca_system_candidate":false,"about_ca_system_consensus":false,"about_ca_system_score_codex":0.0002829013,"about_ca_system_score_gemma":0.0002683526,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_topic_score_codex":0.007908585,"about_ca_topic_score_gemma":0.004778704,"domain_scores_codex":[0.9997358,0.00006748904,0.00002030594,0.0001016407,0.00004037187,0.00003437522],"domain_scores_gemma":[0.9995491,0.0001137387,0.0002198459,0.0000420828,0.00002897529,0.00004627731],"domain_codex":null,"domain_gemma":null,"domain_candidate":null,"domain_consensus":null,"study_design_codex":"observational","study_design_gemma":"observational","study_design_scores_codex":[0.0007545447,0.00004176613,0.9904207,0.00003050609,0.000201579,0.0002656786,0.0001976095,0.00009835485,0.004725656,0.00004554498,0.00006037972,0.003157732],"study_design_scores_gemma":[0.0000224583,0.0001410041,0.9981064,0.00000632803,0.0001318057,0.0003890193,0.0001186665,0.0002248707,0.0005299143,0.00002988496,0.000296698,0.000003016147],"study_design_candidate":"observational","study_design_consensus":"observational","genre_codex":"empirical","genre_gemma":"empirical","genre_scores_codex":[0.999522,0.0001279087,0.0000945685,0.00001676286,8.839097e-7,0.000002635836,0.0001513154,0.000002558087,0.00008136058],"genre_scores_gemma":[0.9991009,0.0001174181,0.0003317431,0.00001681583,0.000003419961,0.00001022196,0.0002850312,0.000004634078,0.0001296624],"genre_candidate":"empirical","genre_consensus":"empirical","teacher_disagreement_score":0.007908585,"threshold_uncertainty_score":0.01572508,"prediction_status":"machine_predicted_unvalidated"},"labels":[],"label_agreement":null},{"id":"W2294727991","doi":"10.1186/s12881-016-0284-4","title":"12 year follow up of enzyme-replacement therapy in two siblings with attenuated mucopolysaccharidosis I: the important role of early treatment","year":2016,"lang":"en","type":"article","venue":"BMC Medical Genetics","topic":"Lysosomal Storage Disorders Research","field":"Medicine","cited_by":64,"is_retracted":false,"has_abstract":true,"routes":{"ca_aff":true,"ca_fund":false,"ca_venue":false,"about_ca":false},"ca_institutions":"University of British Columbia; Child and Family Research Institute","funders":"Università degli Studi di Perugia","keywords":"Enzyme replacement therapy; Mucopolysaccharidosis; Mucopolysaccharidosis I; Hurler syndrome; Mucopolysaccharidosis type I; Medicine; Disease; Pediatrics; Lysosomal storage disease; Internal medicine","authors":[{"name":"Orazio Gabrielli","is_ca":false},{"name":"L. Clarke","is_ca":true},{"name":"Anna Ficcadenti","is_ca":false},{"name":"Lucia Santoro","is_ca":false},{"name":"Lucia Zampini","is_ca":false},{"name":"Nicola Volpi","is_ca":false},{"name":"Giovanni V. Coppa","is_ca":false}],"retraction":null,"screen_n_in":null,"score":{"opus":0.03332591971994221,"gpt":0.3167682879465656,"spread":0.2834423682266234,"validation_status":"score_only:v0-immature-baseline"},"prediction":{"model_version":"metacan-v3-hybrid-931329e0061c","candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0003559605,0.0006633492,0.0008140811,0.0007816342,0.001267642,0.0005054715,0.0004104804,0.001794778,0.0007301843],"category_scores_gemma":[0.002185374,0.000357406,0.0008897248,0.0004571882,0.0005916585,0.0005260585,0.0005106698,0.00155069,0.0003535154],"about_ca_system_candidate":false,"about_ca_system_consensus":false,"about_ca_system_score_codex":0.0006967415,"about_ca_system_score_gemma":0.0004646515,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_topic_score_codex":0.003355236,"about_ca_topic_score_gemma":0.0020843,"domain_scores_codex":[0.9995863,0.0000744496,0.00006323983,0.00009563265,0.00007495555,0.0001053868],"domain_scores_gemma":[0.9986321,0.0002667497,0.000317278,0.00007870742,0.0001625485,0.0005426403],"domain_codex":null,"domain_gemma":null,"domain_candidate":null,"domain_consensus":null,"study_design_codex":"observational","study_design_gemma":"observational","study_design_scores_codex":[0.001040969,0.0008742749,0.543375,0.00005918303,0.0001214453,0.4336131,0.002272948,0.0003743752,0.008272986,0.000104893,0.0003748712,0.009516054],"study_design_scores_gemma":[0.00009759017,0.00416067,0.6183235,0.00004077595,0.0002581387,0.3703627,0.001026368,0.0006413455,0.002990031,0.0001141166,0.001921227,0.00006354688],"study_design_candidate":"observational","study_design_consensus":"observational","genre_codex":"empirical","genre_gemma":"empirical","genre_scores_codex":[0.9981537,0.0005767102,0.0002120882,0.0001683136,0.0000263958,0.00001361384,0.00007855808,0.00001385965,0.0007565992],"genre_scores_gemma":[0.9991346,0.0001501098,0.000133249,0.0001146357,0.00002669734,0.000006580033,0.0001436841,0.000004716533,0.0002857254],"genre_candidate":"empirical","genre_consensus":"empirical","teacher_disagreement_score":0.003355236,"threshold_uncertainty_score":0.006671429,"prediction_status":"machine_predicted_unvalidated"},"labels":[],"label_agreement":null},{"id":"W2088239147","doi":"10.1186/1471-2350-5-17","title":"Phenotypic and molecular assessment of seven patients with 6p25 deletion syndrome: Relevance to ocular dysgenesis and hearing impairment","year":2004,"lang":"en","type":"review","venue":"BMC Medical Genetics","topic":"Genomic variations and chromosomal abnormalities","field":"Biochemistry, Genetics and Molecular Biology","cited_by":63,"is_retracted":false,"has_abstract":true,"routes":{"ca_aff":true,"ca_fund":true,"ca_venue":false,"about_ca":false},"ca_institutions":"University of Alberta","funders":"Canadian Institutes of Health Research; Alberta Heritage Foundation for Medical Research; Fondation pour la Recherche Médicale; Schweizerischer Nationalfonds zur Förderung der Wissenschaftlichen Forschung; National Science Foundation","keywords":"Genetics; Biology; Locus (genetics); Hearing loss; Phenotype; Dysgenesis; Genetic heterogeneity; Gene; Medicine; Audiology","authors":[{"name":"Douglas B. Gould","is_ca":true},{"name":"Mohamad S. Jaafar","is_ca":false},{"name":"MarkK. Addison","is_ca":false},{"name":"Francis L. Munier","is_ca":false},{"name":"Robert Ritch","is_ca":false},{"name":"Ian M. MacDonald","is_ca":true},{"name":"Michael A. Walter","is_ca":true}],"retraction":null,"screen_n_in":null,"score":{"opus":0.01055479440923914,"gpt":0.2731905563744201,"spread":0.262635761965181,"validation_status":"score_only:v0-immature-baseline"},"prediction":{"model_version":"metacan-v3-hybrid-931329e0061c","candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.000148785,0.0008025129,0.0003085201,0.0007471823,0.0004853036,0.0003315766,0.0002434291,0.0004252927,0.001665111],"category_scores_gemma":[0.0009517609,0.0002335779,0.0002721702,0.0003453949,0.0004688183,0.0001583181,0.0004026236,0.0002969095,0.0002990675],"about_ca_system_candidate":false,"about_ca_system_consensus":false,"about_ca_system_score_codex":0.0002923367,"about_ca_system_score_gemma":0.0002203215,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_topic_score_codex":0.000943266,"about_ca_topic_score_gemma":0.0008170428,"domain_scores_codex":[0.9998105,0.00002040795,0.0000265929,0.00005528521,0.00004363959,0.00004361845],"domain_scores_gemma":[0.9996905,0.00007357896,0.00006625438,0.0000196225,0.00003488868,0.0001151668],"domain_codex":null,"domain_gemma":null,"domain_candidate":null,"domain_consensus":null,"study_design_codex":"observational","study_design_gemma":"case_report","study_design_scores_codex":[0.0006144718,0.0002626085,0.7234938,0.0001197636,0.00007741225,0.1722495,0.002003673,0.0006436316,0.07852475,0.0002737223,0.0004978126,0.02123881],"study_design_scores_gemma":[0.0001026866,0.00120157,0.6841633,0.00003122368,0.0001585574,0.2952938,0.0009036149,0.0009242758,0.01464274,0.0003183954,0.002204614,0.00005532791],"study_design_candidate":"case_report","study_design_consensus":null,"genre_codex":"empirical","genre_gemma":"review","genre_scores_codex":[0.9993027,0.00006926932,0.0002292211,0.00001877265,0.000001937276,0.000008071244,0.00005654902,0.000007767861,0.0003056965],"genre_scores_gemma":[0.9990143,0.00007714232,0.0004760188,0.00002278304,0.000003686135,0.00001203986,0.0001725248,0.000004589337,0.0002168679],"genre_candidate":"review","genre_consensus":null,"teacher_disagreement_score":0.001665111,"threshold_uncertainty_score":0.005570352,"prediction_status":"machine_predicted_unvalidated"},"labels":[],"label_agreement":null},{"id":"W2003897274","doi":"10.1186/1471-2350-9-116","title":"Selecting a BRCA risk assessment model for use in a familial cancer clinic","year":2008,"lang":"en","type":"article","venue":"BMC Medical Genetics","topic":"BRCA gene mutations in cancer","field":"Biochemistry, Genetics and Molecular Biology","cited_by":61,"is_retracted":false,"has_abstract":true,"routes":{"ca_aff":true,"ca_fund":false,"ca_venue":false,"about_ca":false},"ca_institutions":"Statistics Canada; University of Toronto; Mount Sinai Hospital","funders":"","keywords":"Medicine; Receiver operating characteristic; Ibis; Proband; Genetic testing; BRCA mutation; Mutation; Cancer; Oncology; Genetics; Internal medicine; Breast cancer; Biology; Gene","authors":[{"name":"Seema Panchal","is_ca":true},{"name":"Marguerite Ennis","is_ca":true},{"name":"Sandra Constanza Mgth Cañón","is_ca":true},{"name":"Louise Bordeleau","is_ca":true}],"retraction":null,"screen_n_in":null,"score":{"opus":0.07389192723062177,"gpt":0.3789553276209157,"spread":0.3050634003902939,"validation_status":"score_only:v0-immature-baseline"},"prediction":{"model_version":"metacan-v3-hybrid-931329e0061c","candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.005571996,0.0007302925,0.0007399744,0.001057693,0.000364947,0.0009627265,0.0007158837,0.0005535331,0.001575026],"category_scores_gemma":[0.01536749,0.0003351906,0.0007190881,0.0004855315,0.0001869609,0.0003858612,0.0005942485,0.0006708548,0.0003239858],"about_ca_system_candidate":false,"about_ca_system_consensus":false,"about_ca_system_score_codex":0.001071447,"about_ca_system_score_gemma":0.001155005,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_topic_score_codex":0.01165539,"about_ca_topic_score_gemma":0.008846305,"domain_scores_codex":[0.9987081,0.00075925,0.00005523242,0.0002462285,0.0001398655,0.00009123916],"domain_scores_gemma":[0.9917858,0.006773967,0.0005709637,0.0001976223,0.0004697733,0.0002018921],"domain_codex":null,"domain_gemma":null,"domain_candidate":null,"domain_consensus":null,"study_design_codex":"observational","study_design_gemma":"theoretical_or_conceptual","study_design_scores_codex":[0.002441602,0.0004889866,0.5862146,0.0001207226,0.000639015,0.0008664692,0.0005196607,0.3214069,0.00144898,0.001262832,0.004136427,0.08045387],"study_design_scores_gemma":[0.0001485642,0.0004318435,0.03850872,0.00004477298,0.0002167192,0.0004880556,0.0001359404,0.9565217,0.0006680453,0.001989478,0.0008158955,0.00003015742],"study_design_candidate":"theoretical_or_conceptual","study_design_consensus":null,"genre_codex":"empirical","genre_gemma":"empirical","genre_scores_codex":[0.9280602,0.0002453009,0.06875701,0.0005526328,0.00001426615,0.000207714,0.0003726824,0.0004262823,0.001363837],"genre_scores_gemma":[0.9736832,0.00006136809,0.02533136,0.0000700716,0.000009276274,0.0001032346,0.0003613301,0.00002115661,0.0003589991],"genre_candidate":"empirical","genre_consensus":"empirical","teacher_disagreement_score":0.01165539,"threshold_uncertainty_score":0.02946788,"prediction_status":"machine_predicted_unvalidated"},"labels":[],"label_agreement":null},{"id":"W1644098900","doi":"10.1186/1471-2350-5-30","title":"Catechol-O-Methyltransferase (COMT) Val 108/158 Metpolymorphism does not modulate executive function in children with ADHD","year":2004,"lang":"en","type":"article","venue":"BMC Medical Genetics","topic":"Attention Deficit Hyperactivity Disorder","field":"Medicine","cited_by":60,"is_retracted":false,"has_abstract":true,"routes":{"ca_aff":true,"ca_fund":true,"ca_venue":false,"about_ca":false},"ca_institutions":"McGill University; Douglas Mental Health University Institute","funders":"Canadian Institutes of Health Research","keywords":"Catechol-O-methyl transferase; Wisconsin Card Sorting Test; Executive functions; Psychology; Prefrontal cortex; Neuropsychology; Continuous performance task; Cognition; Neuropsychological test; Clinical psychology; Genotype; Psychiatry; Developmental psychology; Genetics; Gene; Biology","authors":[{"name":"Evan Taerk","is_ca":true},{"name":"Natalie Grizenko","is_ca":true},{"name":"Leila Ben Amor","is_ca":true},{"name":"Philippe Lageix","is_ca":true},{"name":"Valentin Mbékou","is_ca":true},{"name":"Rosherie Deguzman","is_ca":true},{"name":"Adam Torkamanzehi","is_ca":true},{"name":"Marina Ter Stepanian","is_ca":true},{"name":"Chantal Baron","is_ca":true},{"name":"Ridha Joober","is_ca":true}],"retraction":null,"screen_n_in":null,"score":{"opus":0.03000998640808698,"gpt":0.2926043728316087,"spread":0.2625943864235217,"validation_status":"score_only:v0-immature-baseline"},"prediction":{"model_version":"metacan-v3-hybrid-931329e0061c","candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0002721185,0.0005078466,0.0003741268,0.0004570361,0.0002666476,0.0004216824,0.0002686887,0.0003755036,0.00216667],"category_scores_gemma":[0.001633894,0.0001697804,0.0002827319,0.0004199379,0.000384701,0.0001559055,0.0002024851,0.0003552997,0.0001881839],"about_ca_system_candidate":false,"about_ca_system_consensus":false,"about_ca_system_score_codex":0.0002812033,"about_ca_system_score_gemma":0.0002326609,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_topic_score_codex":0.005027305,"about_ca_topic_score_gemma":0.005239035,"domain_scores_codex":[0.9997306,0.00005281409,0.00003996766,0.00007627674,0.00006601239,0.00003426945],"domain_scores_gemma":[0.9991943,0.0002085892,0.0004231586,0.0000458531,0.00004496322,0.00008311956],"domain_codex":null,"domain_gemma":null,"domain_candidate":null,"domain_consensus":null,"study_design_codex":"observational","study_design_gemma":"observational","study_design_scores_codex":[0.0008264626,0.0001030375,0.9817722,0.00003721932,0.0001637077,0.001349679,0.0002466454,0.0001112347,0.01174011,0.00005536384,0.0001215062,0.003472897],"study_design_scores_gemma":[0.00002753415,0.0001989586,0.9959928,0.00001159833,0.00006540475,0.002630844,0.0001492468,0.0001337347,0.0005921237,0.00003636426,0.0001582381,0.000003119429],"study_design_candidate":"observational","study_design_consensus":"observational","genre_codex":"empirical","genre_gemma":"empirical","genre_scores_codex":[0.9995309,0.000105122,0.00004169916,0.00002535531,0.00000378391,0.000002280241,0.0001171904,0.000003599067,0.0001701177],"genre_scores_gemma":[0.9995091,0.00006942709,0.0001078879,0.00001604201,0.00000466378,0.00000373649,0.0001976185,0.000005151853,0.00008643317],"genre_candidate":"empirical","genre_consensus":"empirical","teacher_disagreement_score":0.005027305,"threshold_uncertainty_score":0.009996057,"prediction_status":"machine_predicted_unvalidated"},"labels":[],"label_agreement":null},{"id":"W2092791760","doi":"10.1186/1471-2350-12-10","title":"Testing the thrifty gene hypothesis: the Gly482Ser variant in PPARGC1Ais associated with BMI in Tongans","year":2011,"lang":"en","type":"article","venue":"BMC Medical Genetics","topic":"Peroxisome Proliferator-Activated Receptors","field":"Biochemistry, Genetics and Molecular Biology","cited_by":60,"is_retracted":false,"has_abstract":true,"routes":{"ca_aff":true,"ca_fund":true,"ca_venue":false,"about_ca":false},"ca_institutions":"Acadia University","funders":"Max-Planck-Gesellschaft; Acadia University; U.S. Department of Agriculture","keywords":"Human genetics; Genetics; Biology; Evolutionary biology; Statistical hypothesis testing; Computational biology; Gene; Bioinformatics; Statistics; Mathematics","authors":[{"name":"Sean Myles","is_ca":true},{"name":"Rod A. Lea","is_ca":false},{"name":"Jun Ohashi","is_ca":false},{"name":"Geoffrey K. Chambers","is_ca":false},{"name":"Joerg Weiss","is_ca":true},{"name":"Emilie A. Hardouin","is_ca":false},{"name":"Johannes Engelken","is_ca":false},{"name":"Donia Macartney‐Coxson","is_ca":false},{"name":"David Eccles","is_ca":false},{"name":"Izumi Naka","is_ca":false},{"name":"Ryosuke Kimura","is_ca":false},{"name":"Tsukasa Inaoka","is_ca":false},{"name":"Yasuhiro Matsumura","is_ca":false},{"name":"Mark Stoneking","is_ca":false}],"retraction":null,"screen_n_in":null,"score":{"opus":0.05581088611394051,"gpt":0.2364361658732711,"spread":0.1806252797593306,"validation_status":"score_only:v0-immature-baseline"},"prediction":{"model_version":"metacan-v3-hybrid-931329e0061c","candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0004407388,0.0002657211,0.0002276421,0.0005033764,0.0006265186,0.0002975287,0.0003383519,0.0002862558,0.002139088],"category_scores_gemma":[0.001164799,0.0001739905,0.0004125794,0.0006256758,0.0005988249,0.0001844805,0.0005305904,0.0003716073,0.00009136287],"about_ca_system_candidate":false,"about_ca_system_consensus":false,"about_ca_system_score_codex":0.0003155756,"about_ca_system_score_gemma":0.0003417181,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_topic_score_codex":0.0279124,"about_ca_topic_score_gemma":0.02817531,"domain_scores_codex":[0.9997914,0.00005054471,0.00002205576,0.00006110033,0.000033919,0.00004096136],"domain_scores_gemma":[0.9994327,0.0001150307,0.0002115331,0.00005533958,0.00006134905,0.0001240462],"domain_codex":null,"domain_gemma":null,"domain_candidate":null,"domain_consensus":null,"study_design_codex":"observational","study_design_gemma":"observational","study_design_scores_codex":[0.0001039898,0.00001050401,0.9953506,0.000009794158,0.00008044558,0.0002002293,0.0002541835,0.00003038602,0.0033347,0.0000212116,0.00002210385,0.0005818818],"study_design_scores_gemma":[0.000003621855,0.00003386277,0.9991234,0.000002958904,0.00003453325,0.0001957304,0.0002339001,0.0001422903,0.0001622936,0.00001400243,0.00005167169,0.00000168277],"study_design_candidate":"observational","study_design_consensus":"observational","genre_codex":"empirical","genre_gemma":"empirical","genre_scores_codex":[0.9998276,0.00002031922,0.00003975643,0.0000125034,0.000001075331,0.000001638248,0.00003006341,7.631723e-7,0.00006610826],"genre_scores_gemma":[0.9997608,0.00001561952,0.00007995285,0.00001211161,0.000001393323,0.000002850153,0.00004462388,9.082146e-7,0.00008172393],"genre_candidate":"empirical","genre_consensus":"empirical","teacher_disagreement_score":0.0279124,"threshold_uncertainty_score":0.05549985,"prediction_status":"machine_predicted_unvalidated"},"labels":[],"label_agreement":null},{"id":"W2111154371","doi":"10.1186/1471-2350-12-137","title":"Pharmacogenetic analysis of the effects of polymorphisms in APOE, IDE and IL1B on a ketone body based therapeutic on cognition in mild to moderate Alzheimer's disease; a randomized, double-blind, placebo-controlled study","year":2011,"lang":"en","type":"article","venue":"BMC Medical Genetics","topic":"Diet and metabolism studies","field":"Medicine","cited_by":59,"is_retracted":false,"has_abstract":true,"routes":{"ca_aff":true,"ca_fund":false,"ca_venue":false,"about_ca":false},"ca_institutions":"Douglas College","funders":"","keywords":"Apolipoprotein E; Placebo; Pharmacogenetics; Genotype; Polymorphism (computer science); Alzheimer's disease; Medicine; Internal medicine; Randomized controlled trial; Allele; Dementia; Disease; Oncology; Psychology; Genetics; Biology; Gene; Pathology","authors":[{"name":"Samuel T. Henderson","is_ca":false},{"name":"Judes Poirier","is_ca":true}],"retraction":null,"screen_n_in":null,"score":{"opus":0.05666403679908684,"gpt":0.3295646466119551,"spread":0.2729006098128682,"validation_status":"score_only:v0-immature-baseline"},"prediction":{"model_version":"metacan-v3-hybrid-931329e0061c","candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.001919529,0.001352415,0.002727822,0.0005827122,0.0005378057,0.0006736437,0.000843258,0.001653286,0.003541514],"category_scores_gemma":[0.002498832,0.0006210506,0.00163155,0.0005406157,0.001107029,0.0005020131,0.0003351082,0.001451632,0.000350329],"about_ca_system_candidate":false,"about_ca_system_consensus":false,"about_ca_system_score_codex":0.0005188838,"about_ca_system_score_gemma":0.0007086972,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_topic_score_codex":0.0007177654,"about_ca_topic_score_gemma":0.001137574,"domain_scores_codex":[0.9987454,0.0007254045,0.0001175472,0.0001938681,0.0001119191,0.0001058212],"domain_scores_gemma":[0.9984193,0.000600016,0.0003964411,0.0001456164,0.0001148259,0.0003237761],"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":[0.9825423,0.008300381,0.0009278763,0.0002569371,0.0009917613,0.00002076754,0.00002470203,0.00007940707,0.002509104,0.00002320001,0.00007707289,0.004246525],"study_design_scores_gemma":[0.8432656,0.1457888,0.00772933,0.00002352896,0.001731671,0.00002717971,0.0000151071,0.0003050959,0.0008046288,0.0001054323,0.0001884042,0.00001534799],"study_design_candidate":"randomized_trial","study_design_consensus":"randomized_trial","genre_codex":"empirical","genre_gemma":"empirical","genre_scores_codex":[0.996191,0.001433568,0.0003517011,0.000141047,0.0001457586,0.001111353,0.0002543295,0.00002467326,0.0003466549],"genre_scores_gemma":[0.9952227,0.0007798614,0.0009075914,0.0002565928,0.0002559342,0.001684553,0.0002319565,0.000008125787,0.0006526275],"genre_candidate":"empirical","genre_consensus":"empirical","teacher_disagreement_score":0.003541514,"threshold_uncertainty_score":0.0118475,"prediction_status":"machine_predicted_unvalidated"},"labels":[],"label_agreement":null},{"id":"W2040127176","doi":"10.1186/1471-2350-8-11","title":"Case-control and family-based association studies of candidate genes in autistic disorder and its endophenotypes: TPH2 and GLO1","year":2007,"lang":"en","type":"article","venue":"BMC Medical Genetics","topic":"Autism Spectrum Disorder Research","field":"Neuroscience","cited_by":57,"is_retracted":false,"has_abstract":true,"routes":{"ca_aff":true,"ca_fund":false,"ca_venue":false,"about_ca":false},"ca_institutions":"Ontario Genomics; University of Toronto","funders":"","keywords":"TPH2; Autism; Macrocephaly; Endophenotype; Genetics; Autism spectrum disorder; Biology; Haplotype; Single-nucleotide polymorphism; Allele; Transmission disequilibrium test; Serotonergic; Psychology; Gene; Genotype; Neuroscience; Psychiatry; Serotonin","authors":[{"name":"Roberto Sacco","is_ca":false},{"name":"Veruska Papaleo","is_ca":false},{"name":"Jörg Hager","is_ca":false},{"name":"Francis Rousseau","is_ca":false},{"name":"Rainald Moessner","is_ca":true},{"name":"Roberto Militerni","is_ca":false},{"name":"Carmela Bravaccio","is_ca":false},{"name":"Simona Trillo","is_ca":false},{"name":"Cindy Schneider","is_ca":false},{"name":"Raun D. Melmed","is_ca":false},{"name":"Maurizio Elia","is_ca":false},{"name":"Paolo Curatolo","is_ca":false},{"name":"Barbara Manzi","is_ca":false},{"name":"Tiziana Pascucci","is_ca":false},{"name":"Stefano Puglisi‐Allegra","is_ca":false},{"name":"Karl-Ludvig Reichelt","is_ca":false},{"name":"Antonio M. Persico","is_ca":false}],"retraction":null,"screen_n_in":null,"score":{"opus":0.04146076676226261,"gpt":0.3330431809583745,"spread":0.2915824141961119,"validation_status":"score_only:v0-immature-baseline"},"prediction":{"model_version":"metacan-v3-hybrid-931329e0061c","candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.001551579,0.0006278384,0.0005368666,0.001958129,0.0007742724,0.0005059803,0.0005332372,0.000553821,0.002437632],"category_scores_gemma":[0.005747188,0.0003219325,0.0005074909,0.001376605,0.00057411,0.000234441,0.0006068508,0.0003233693,0.0001888994],"about_ca_system_candidate":false,"about_ca_system_consensus":false,"about_ca_system_score_codex":0.0003376374,"about_ca_system_score_gemma":0.0002205532,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_topic_score_codex":0.003836261,"about_ca_topic_score_gemma":0.002828237,"domain_scores_codex":[0.9978764,0.0007429273,0.0001979969,0.0007721465,0.000298829,0.0001117423],"domain_scores_gemma":[0.9971853,0.001257423,0.0007072534,0.0003615059,0.0002341313,0.0002543241],"domain_codex":null,"domain_gemma":null,"domain_candidate":null,"domain_consensus":null,"study_design_codex":"observational","study_design_gemma":"observational","study_design_scores_codex":[0.001066155,0.0000871638,0.986626,0.0000304107,0.0005483293,0.0025444,0.0004059486,0.0001571392,0.004847315,0.0001100075,0.0001479184,0.003429115],"study_design_scores_gemma":[0.0000690974,0.0002418229,0.9911227,0.00001179308,0.0002949322,0.00633396,0.0001664316,0.0005304583,0.0007809034,0.00009432541,0.0003430496,0.00001051657],"study_design_candidate":"observational","study_design_consensus":"observational","genre_codex":"empirical","genre_gemma":"empirical","genre_scores_codex":[0.9989265,0.0002181485,0.0004185778,0.00001578521,0.00000399678,0.00001459323,0.0001389896,0.000007140348,0.0002563055],"genre_scores_gemma":[0.9993194,0.00006886027,0.0003295869,0.000009521971,0.00000550916,0.00001653217,0.0001622847,0.000003188749,0.00008508453],"genre_candidate":"empirical","genre_consensus":"empirical","teacher_disagreement_score":0.003836261,"threshold_uncertainty_score":0.008205652,"prediction_status":"machine_predicted_unvalidated"},"labels":[],"label_agreement":null},{"id":"W2162249830","doi":"10.1186/1471-2350-11-50","title":"Allelic variants of IL1R1gene associate with severe hand osteoarthritis","year":2010,"lang":"en","type":"article","venue":"BMC Medical Genetics","topic":"Osteoarthritis Treatment and Mechanisms","field":"Medicine","cited_by":53,"is_retracted":false,"has_abstract":true,"routes":{"ca_aff":true,"ca_fund":false,"ca_venue":false,"about_ca":false},"ca_institutions":"University of Alberta","funders":"Academy of Finland","keywords":"Single-nucleotide polymorphism; Genetics; Locus (genetics); Haplotype; Candidate gene; Biology; SNP; Genetic association; Genetic linkage; Genome-wide association study; Gene; Tag SNP; Allele; Linkage disequilibrium; Population; Genotype; Medicine","authors":[{"name":"Annu Näkki","is_ca":false},{"name":"Sanna T Kouhia","is_ca":false},{"name":"Janna Saarela","is_ca":false},{"name":"Arsi Harilainen","is_ca":false},{"name":"Kaj Tallroth","is_ca":false},{"name":"Tapio Videman","is_ca":true},{"name":"Michele C. Battié","is_ca":true},{"name":"Jaakko Kaprio","is_ca":false},{"name":"Leena Peltonen","is_ca":false},{"name":"Urho M. Kujala","is_ca":false}],"retraction":null,"screen_n_in":null,"score":{"opus":0.01178317385103497,"gpt":0.2469186990655075,"spread":0.2351355252144725,"validation_status":"score_only:v0-immature-baseline"},"prediction":{"model_version":"metacan-v3-hybrid-931329e0061c","candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0004466803,0.0006384286,0.0004073465,0.0007063373,0.0003926726,0.0003412194,0.0003625648,0.0005200328,0.006224925],"category_scores_gemma":[0.001428178,0.0002097585,0.0003225561,0.0007570227,0.0003977584,0.0001223272,0.0003520199,0.0004817783,0.0004286898],"about_ca_system_candidate":false,"about_ca_system_consensus":false,"about_ca_system_score_codex":0.0001368727,"about_ca_system_score_gemma":0.0001657812,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_topic_score_codex":0.0008656716,"about_ca_topic_score_gemma":0.001097105,"domain_scores_codex":[0.9995384,0.0001188316,0.00004981976,0.0001664367,0.00007559459,0.0000509923],"domain_scores_gemma":[0.9983719,0.0005532534,0.0007446797,0.0001074303,0.00006542456,0.0001572558],"domain_codex":null,"domain_gemma":null,"domain_candidate":null,"domain_consensus":null,"study_design_codex":"observational","study_design_gemma":"observational","study_design_scores_codex":[0.001663853,0.0001776197,0.9348411,0.000143715,0.0005438859,0.006352969,0.0004111241,0.0005002607,0.04521376,0.0002994796,0.0005779882,0.00927432],"study_design_scores_gemma":[0.00005838802,0.0002199279,0.9854349,0.00001828097,0.0001855125,0.01127112,0.00009746025,0.0003035622,0.001687397,0.0002310463,0.0004827537,0.000009730808],"study_design_candidate":"observational","study_design_consensus":"observational","genre_codex":"empirical","genre_gemma":"empirical","genre_scores_codex":[0.9982823,0.0004413407,0.0005026087,0.00005919371,0.000006890958,0.000008283373,0.0002449413,0.00002057535,0.0004337417],"genre_scores_gemma":[0.9988165,0.0001268045,0.0004828206,0.00002518481,0.00002578439,0.000007059467,0.0002383162,0.000006622156,0.0002708632],"genre_candidate":"empirical","genre_consensus":"empirical","teacher_disagreement_score":0.006224925,"threshold_uncertainty_score":0.02082449,"prediction_status":"machine_predicted_unvalidated"},"labels":[],"label_agreement":null},{"id":"W2135794732","doi":"10.1186/1471-2350-14-117","title":"The association between the angiotensin-converting enzyme-2 gene and blood pressure in a cohort study of adolescents","year":2013,"lang":"en","type":"article","venue":"BMC Medical Genetics","topic":"Renin-Angiotensin System Studies","field":"Medicine","cited_by":53,"is_retracted":false,"has_abstract":true,"routes":{"ca_aff":true,"ca_fund":true,"ca_venue":false,"about_ca":true},"ca_institutions":"Centre Hospitalier Universitaire Sainte-Justine; University of Ottawa; Centre Hospitalier de l’Université de Montréal; McGill University; Université de Montréal; McGill University Health Centre","funders":"Canadian Institutes of Health Research; McGill University; Heart and Stroke Foundation of Canada; American Heart Association","keywords":"Blood pressure; Single-nucleotide polymorphism; Cohort; Internal medicine; Cohort study; Medicine; Endocrinology; Biology; Genetics; Oncology; Gene; Genotype","authors":[{"name":"Lucile Malard","is_ca":true},{"name":"Lisa Kakinami","is_ca":true},{"name":"Jennifer O’Loughlin","is_ca":true},{"name":"Marie‐Hélène Roy‐Gagnon","is_ca":true},{"name":"Aurélie Labbe","is_ca":true},{"name":"Louise Pilote","is_ca":true},{"name":"Pavel Hamet","is_ca":true},{"name":"Johanne Tremblay","is_ca":true},{"name":"Gilles Paradis","is_ca":true}],"retraction":null,"screen_n_in":null,"score":{"opus":0.01608393316788283,"gpt":0.2609330214990626,"spread":0.2448490883311797,"validation_status":"score_only:v0-immature-baseline"},"prediction":{"model_version":"metacan-v3-hybrid-931329e0061c","candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.001010434,0.0003645277,0.0003885416,0.0006020637,0.0005562784,0.0006566127,0.0003517646,0.0004073212,0.000706237],"category_scores_gemma":[0.001627792,0.0003191333,0.0006596369,0.0008630069,0.0002286963,0.0002604699,0.0003451139,0.0007909246,0.0001291784],"about_ca_system_candidate":false,"about_ca_system_consensus":false,"about_ca_system_score_codex":0.0002685794,"about_ca_system_score_gemma":0.0004247927,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_topic_score_codex":0.01233105,"about_ca_topic_score_gemma":0.01291538,"domain_scores_codex":[0.9994903,0.0001452833,0.00004233548,0.0001431212,0.0001121015,0.00006687298],"domain_scores_gemma":[0.9989594,0.0001723765,0.0003126343,0.0001357345,0.0001596762,0.0002601641],"domain_codex":null,"domain_gemma":null,"domain_candidate":null,"domain_consensus":null,"study_design_codex":"observational","study_design_gemma":"observational","study_design_scores_codex":[0.0000896684,0.00002865266,0.9989373,0.000004110182,0.0001179061,0.00007297139,0.00006418159,0.00001012763,0.0002630885,0.00001071316,0.00005494644,0.0003463872],"study_design_scores_gemma":[0.00001064377,0.00006553731,0.9994668,0.000004407612,0.00006481072,0.0001360656,0.00007451385,0.0000560919,0.00002892037,0.000008610483,0.00008212189,0.000001573256],"study_design_candidate":"observational","study_design_consensus":"observational","genre_codex":"empirical","genre_gemma":"empirical","genre_scores_codex":[0.9993306,0.0001380606,0.00008764979,0.00002954672,0.000008393913,0.000009011427,0.0002669811,0.000001743541,0.0001280205],"genre_scores_gemma":[0.9991014,0.0001703036,0.000179302,0.00003871973,0.00001081677,0.0000188101,0.0003529714,0.000002640618,0.0001251106],"genre_candidate":"empirical","genre_consensus":"empirical","teacher_disagreement_score":0.01233105,"threshold_uncertainty_score":0.02451855,"prediction_status":"machine_predicted_unvalidated"},"labels":[],"label_agreement":null},{"id":"W2549134982","doi":"10.1186/s12881-016-0340-0","title":"Exome sequencing identifies pathogenic variants of VPS13B in a patient with familial 16p11.2 duplication","year":2016,"lang":"en","type":"article","venue":"BMC Medical Genetics","topic":"Blood disorders and treatments","field":"Biochemistry, Genetics and Molecular Biology","cited_by":51,"is_retracted":false,"has_abstract":true,"routes":{"ca_aff":true,"ca_fund":true,"ca_venue":false,"about_ca":false},"ca_institutions":"BC Children's Hospital; Children's & Women's Health Centre of British Columbia","funders":"Canadian Institutes of Health Research; BC Children’s Hospital Foundation; BC Children's Hospital; Children's Hospital Foundation; Child and Family Research Institute","keywords":"Human genetics; Exome sequencing; Gene duplication; Genetics; Biology; Exome; Cytogenetics; Computational biology; Bioinformatics; Mutation; Chromosome; Gene","authors":[{"name":"Jila Dastan","is_ca":true},{"name":"Chieko Chijiwa","is_ca":true},{"name":"Flamingo Tang","is_ca":true},{"name":"Sally Martell","is_ca":true},{"name":"Ying Qiao","is_ca":true},{"name":"Evica Rajcan‐Separovic","is_ca":true},{"name":"M. E. Suzanne Lewis","is_ca":true}],"retraction":null,"screen_n_in":null,"score":{"opus":0.01134563051297505,"gpt":0.2341566374189774,"spread":0.2228110069060023,"validation_status":"score_only:v0-immature-baseline"},"prediction":{"model_version":"metacan-v3-hybrid-931329e0061c","candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0001757577,0.001122964,0.0004670764,0.001036973,0.0006993918,0.0004896435,0.0004553834,0.001910202,0.001289745],"category_scores_gemma":[0.0008932197,0.0003561339,0.0003520915,0.0006139261,0.0005793074,0.0002375243,0.0006206488,0.0005936369,0.0002535042],"about_ca_system_candidate":false,"about_ca_system_consensus":false,"about_ca_system_score_codex":0.0004122456,"about_ca_system_score_gemma":0.0002902508,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_topic_score_codex":0.00201552,"about_ca_topic_score_gemma":0.002502955,"domain_scores_codex":[0.999725,0.00002206121,0.00003017913,0.0001145618,0.0000598791,0.00004835557],"domain_scores_gemma":[0.999612,0.0001557764,0.00007457416,0.00001755447,0.00002876365,0.000111398],"domain_codex":null,"domain_gemma":null,"domain_candidate":null,"domain_consensus":null,"study_design_codex":"case_report","study_design_gemma":"case_report","study_design_scores_codex":[0.0002650486,0.00005894996,0.05524518,0.00006186983,0.00004188694,0.8783051,0.001155642,0.0005709335,0.05850742,0.0002205363,0.0004558348,0.005111624],"study_design_scores_gemma":[0.00004363355,0.0002254205,0.1080601,0.00003184869,0.00006095691,0.8779538,0.0003395032,0.001427729,0.01041409,0.0002330321,0.001182027,0.000027952],"study_design_candidate":"case_report","study_design_consensus":"case_report","genre_codex":"empirical","genre_gemma":"empirical","genre_scores_codex":[0.9987514,0.0001758774,0.0003605797,0.0001084502,0.00001008373,0.0000105759,0.0002099229,0.00001713803,0.000355904],"genre_scores_gemma":[0.9987446,0.0001071574,0.000580604,0.00005587706,0.00001365598,0.000008139337,0.0001744167,0.00001061366,0.0003048229],"genre_candidate":"empirical","genre_consensus":"empirical","teacher_disagreement_score":0.00201552,"threshold_uncertainty_score":0.004314661,"prediction_status":"machine_predicted_unvalidated"},"labels":[],"label_agreement":null},{"id":"W2277946576","doi":"10.1186/s12881-016-0276-4","title":"Case report of novel DYRK1A mutations in 2 individuals with syndromic intellectual disability and a review of the literature","year":2016,"lang":"en","type":"review","venue":"BMC Medical Genetics","topic":"Down syndrome and intellectual disability research","field":"Medicine","cited_by":50,"is_retracted":false,"has_abstract":true,"routes":{"ca_aff":true,"ca_fund":true,"ca_venue":false,"about_ca":false},"ca_institutions":"Children's Hospital of Eastern Ontario","funders":"Institute of Genetics; Canadian Institutes of Health Research","keywords":"Microcephaly; Intellectual disability; DYRK1A; Pediatrics; Medicine; Genetics; Down syndrome; Biology","authors":[{"name":"Stephanie M. Luco","is_ca":true},{"name":"Daniela Pohl","is_ca":true},{"name":"Erick Sell","is_ca":true},{"name":"Justin D. Wagner","is_ca":true},{"name":"David A. Dyment","is_ca":true},{"name":"Hussein Daoud","is_ca":true}],"retraction":null,"screen_n_in":null,"score":{"opus":0.09122771651278956,"gpt":0.3982765759554147,"spread":0.3070488594426251,"validation_status":"score_only:v0-immature-baseline"},"prediction":{"model_version":"metacan-v3-hybrid-931329e0061c","candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0005765348,0.002389408,0.002205655,0.007960334,0.00121103,0.002045489,0.002272421,0.003798129,0.002628269],"category_scores_gemma":[0.002137498,0.0008571204,0.001168817,0.004806827,0.001829025,0.001990456,0.001715292,0.001835608,0.001951295],"about_ca_system_candidate":false,"about_ca_system_consensus":false,"about_ca_system_score_codex":0.0008743827,"about_ca_system_score_gemma":0.0008359473,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_topic_score_codex":0.001430826,"about_ca_topic_score_gemma":0.00186369,"domain_scores_codex":[0.9987968,0.0001044136,0.0003847949,0.0003609989,0.0001851928,0.0001677553],"domain_scores_gemma":[0.9986075,0.0004065369,0.0004779103,0.00008440676,0.0001848712,0.0002388194],"domain_codex":null,"domain_gemma":null,"domain_candidate":null,"domain_consensus":null,"study_design_codex":"case_report","study_design_gemma":"case_report","study_design_scores_codex":[0.000037988,0.0000583388,0.006488568,0.001066205,0.0001085265,0.9615959,0.0004146888,0.0001446365,0.00119124,0.00020525,0.004040102,0.02464855],"study_design_scores_gemma":[0.000009672245,0.00002524105,0.003174414,0.0003158285,0.0000882523,0.9871113,0.0002222288,0.0000772279,0.0002112765,0.0001637538,0.008577601,0.00002322142],"study_design_candidate":"case_report","study_design_consensus":"case_report","genre_codex":"review","genre_gemma":"review","genre_scores_codex":[0.2290712,0.723668,0.01117873,0.005237294,0.004946205,0.0006586254,0.001195708,0.0007243932,0.0233198],"genre_scores_gemma":[0.6397784,0.3279545,0.008705053,0.006786396,0.007958682,0.0003010713,0.001609858,0.000165045,0.006740974],"genre_candidate":"review","genre_consensus":"review","teacher_disagreement_score":0.007960334,"threshold_uncertainty_score":0.0087924,"prediction_status":"machine_predicted_unvalidated"},"labels":[],"label_agreement":null},{"id":"W2156174025","doi":"10.1186/s12881-014-0111-8","title":"Paraganglioma and pheochromocytoma upon maternal transmission of SDHDmutations","year":2014,"lang":"en","type":"article","venue":"BMC Medical Genetics","topic":"Adrenal and Paraganglionic Tumors","field":"Medicine","cited_by":50,"is_retracted":false,"has_abstract":true,"routes":{"ca_aff":true,"ca_fund":false,"ca_venue":false,"about_ca":false},"ca_institutions":"BC Cancer Agency","funders":"","keywords":"SDHD; Paraganglioma; Pheochromocytoma; Biology; Genetics; Carcinogenesis; Germline mutation; Mutation; Cancer research; Pathology; Gene; Medicine; Endocrinology","authors":[{"name":"Jean‐Pierre Bayley","is_ca":false},{"name":"Rogier A. Oldenburg","is_ca":false},{"name":"Jennifer Nuk","is_ca":true},{"name":"Attje S. Hoekstra","is_ca":false},{"name":"Conny A. van der Meer","is_ca":false},{"name":"Esther Korpershoek","is_ca":false},{"name":"Barbara McGillivray","is_ca":true},{"name":"Eleonora P.M. Corssmit","is_ca":false},{"name":"Winand N.M. Dinjens","is_ca":false},{"name":"Ronald R. de Krijger","is_ca":false},{"name":"Peter Devilee","is_ca":false},{"name":"Jeroen C. Jansen","is_ca":false},{"name":"Frederik J. Hes","is_ca":false}],"retraction":null,"screen_n_in":null,"score":{"opus":0.01522071647182628,"gpt":0.2805655933843745,"spread":0.2653448769125482,"validation_status":"score_only:v0-immature-baseline"},"prediction":{"model_version":"metacan-v3-hybrid-931329e0061c","candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0002123995,0.0004039226,0.0001845865,0.0005384258,0.0003780473,0.0002398732,0.000275413,0.0005831067,0.002434822],"category_scores_gemma":[0.001379548,0.0002089881,0.0001583048,0.0002455288,0.0005476995,0.0002498626,0.0003685654,0.0004786361,0.0003689164],"about_ca_system_candidate":false,"about_ca_system_consensus":false,"about_ca_system_score_codex":0.0003428836,"about_ca_system_score_gemma":0.0002820201,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_topic_score_codex":0.0007075999,"about_ca_topic_score_gemma":0.0009535504,"domain_scores_codex":[0.9998264,0.00002093877,0.0000115923,0.00004015801,0.00004090994,0.00006016406],"domain_scores_gemma":[0.9992527,0.0002734159,0.0002395716,0.00006614211,0.00003423497,0.0001340028],"domain_codex":null,"domain_gemma":null,"domain_candidate":null,"domain_consensus":null,"study_design_codex":"case_report","study_design_gemma":"observational","study_design_scores_codex":[0.0005048733,0.00007628526,0.1222346,0.0001028935,0.00004781565,0.8102355,0.0004873318,0.0001509685,0.05558845,0.0007655766,0.0002774936,0.009528196],"study_design_scores_gemma":[0.00002632535,0.0002609652,0.07055195,0.00000952225,0.00003760696,0.9152375,0.0001151583,0.0002416829,0.01251003,0.0003505771,0.0006485773,0.00001012258],"study_design_candidate":"observational","study_design_consensus":null,"genre_codex":"empirical","genre_gemma":"empirical","genre_scores_codex":[0.9966343,0.0003936017,0.0009262043,0.00008612557,0.0000150292,0.00001248732,0.00004809637,0.000043631,0.001840533],"genre_scores_gemma":[0.9993018,0.0001066881,0.0002609738,0.00002062653,0.00001659854,0.00000320931,0.00002528211,0.000005060957,0.0002598382],"genre_candidate":"empirical","genre_consensus":"empirical","teacher_disagreement_score":0.002434822,"threshold_uncertainty_score":0.008145273,"prediction_status":"machine_predicted_unvalidated"},"labels":[],"label_agreement":null},{"id":"W1984810097","doi":"10.1186/1471-2350-9-69","title":"Analysis of variants in DNA damage signalling genes in bladder cancer","year":2008,"lang":"en","type":"article","venue":"BMC Medical Genetics","topic":"DNA Repair Mechanisms","field":"Biochemistry, Genetics and Molecular Biology","cited_by":47,"is_retracted":false,"has_abstract":true,"routes":{"ca_aff":true,"ca_fund":false,"ca_venue":false,"about_ca":false},"ca_institutions":"Princess Margaret Cancer Centre; Ontario Institute for Cancer Research","funders":"Cancer Research UK","keywords":"Bladder cancer; Single-nucleotide polymorphism; Biology; DNA damage; Genotype; SNP genotyping; DNA repair; Carcinogenesis; Cancer; Population; Genotyping; Genetics; Oncology; Gene; Medicine; DNA","authors":[{"name":"Ananya Choudhury","is_ca":false},{"name":"Faye Elliott","is_ca":false},{"name":"Mark M. Iles","is_ca":false},{"name":"Michael Churchman","is_ca":false},{"name":"Robert G. Bristow","is_ca":true},{"name":"D. Timothy Bishop","is_ca":false},{"name":"Anne E. Kiltie","is_ca":false}],"retraction":null,"screen_n_in":null,"score":{"opus":0.02366146888860548,"gpt":0.2826810167187251,"spread":0.2590195478301196,"validation_status":"score_only:v0-immature-baseline"},"prediction":{"model_version":"metacan-v3-hybrid-931329e0061c","candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0006533338,0.000353888,0.000383601,0.001127822,0.0003790207,0.0004001708,0.0003717481,0.0007859078,0.002483108],"category_scores_gemma":[0.002004544,0.0002044032,0.0005671984,0.001538284,0.0002445203,0.0001529119,0.0002873399,0.0003745974,0.0002619479],"about_ca_system_candidate":false,"about_ca_system_consensus":false,"about_ca_system_score_codex":0.0002428095,"about_ca_system_score_gemma":0.0002196275,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_topic_score_codex":0.002523815,"about_ca_topic_score_gemma":0.001932587,"domain_scores_codex":[0.9992761,0.0002084538,0.000087118,0.0002393584,0.0001085172,0.00008049157],"domain_scores_gemma":[0.9987627,0.00049969,0.000404957,0.00007008031,0.00009632341,0.0001662595],"domain_codex":null,"domain_gemma":null,"domain_candidate":null,"domain_consensus":null,"study_design_codex":"observational","study_design_gemma":"observational","study_design_scores_codex":[0.0009943672,0.00006732519,0.9812776,0.0000922758,0.0004548745,0.0007911024,0.0001500161,0.000219017,0.01052544,0.0000845547,0.0001363438,0.005207072],"study_design_scores_gemma":[0.00001630081,0.0001711757,0.9969748,0.00001456987,0.0001930654,0.001079112,0.00004483914,0.0002858875,0.0008689272,0.00006865332,0.0002770652,0.000005560991],"study_design_candidate":"observational","study_design_consensus":"observational","genre_codex":"empirical","genre_gemma":"empirical","genre_scores_codex":[0.9984576,0.0006665002,0.0002782922,0.00003966029,0.000008015446,0.000008666491,0.0003026347,0.00001061677,0.0002279936],"genre_scores_gemma":[0.9994443,0.00008679049,0.0001738307,0.00001274724,0.000005072837,0.000005908054,0.000151526,0.000002664178,0.0001170992],"genre_candidate":"empirical","genre_consensus":"empirical","teacher_disagreement_score":0.002523815,"threshold_uncertainty_score":0.008306801,"prediction_status":"machine_predicted_unvalidated"},"labels":[],"label_agreement":null},{"id":"W2102270499","doi":"10.1186/1471-2350-15-36","title":"Compound heterozygous mutations in glycyl-tRNA synthetase are a proposed cause of systemic mitochondrial disease","year":2014,"lang":"en","type":"article","venue":"BMC Medical Genetics","topic":"RNA and protein synthesis mechanisms","field":"Biochemistry, Genetics and Molecular Biology","cited_by":46,"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; McGill University; Ottawa Hospital; Children's Hospital of Eastern Ontario; University of Ottawa","funders":"Institute of Genetics; University of Toronto; Université de Montréal; Genome British Columbia; Canadian Institutes of Health Research; Ontario Genomics; Genome Canada; Government of Canada; McGill University; Ontario Genomics Institute; University of Ottawa","keywords":"Human genetics; Genetics; Transfer RNA; Biology; Mitochondrial disease; Mitochondrial DNA; Cytogenetics; Mutation; Molecular biology; Gene; RNA; Chromosome","authors":[{"name":"Hugh J. McMillan","is_ca":true},{"name":"Jeremy Schwartzentruber","is_ca":true},{"name":"Amanda Smith","is_ca":true},{"name":"Suzie Lee","is_ca":true},{"name":"Pranesh Chakraborty","is_ca":true},{"name":"Dennis E. Bulman","is_ca":true},{"name":"Chandree L. Beaulieu","is_ca":true},{"name":"Jacek Majewski","is_ca":true},{"name":"Kym M. Boycott","is_ca":true},{"name":"Michael T. Geraghty","is_ca":true}],"retraction":null,"screen_n_in":null,"score":{"opus":0.01615439086994317,"gpt":0.2576963334833691,"spread":0.241541942613426,"validation_status":"score_only:v0-immature-baseline"},"prediction":{"model_version":"metacan-v3-hybrid-931329e0061c","candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0001591386,0.001123899,0.0004562013,0.0007758012,0.0004289512,0.00029912,0.0003762243,0.001155945,0.002895891],"category_scores_gemma":[0.000558017,0.0001683017,0.0002043792,0.0006059088,0.0006485194,0.0002475789,0.0004113684,0.0003145573,0.0005371535],"about_ca_system_candidate":false,"about_ca_system_consensus":false,"about_ca_system_score_codex":0.0002255219,"about_ca_system_score_gemma":0.0002059693,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_topic_score_codex":0.0002669974,"about_ca_topic_score_gemma":0.0002817269,"domain_scores_codex":[0.9998726,0.00001869386,0.00001652943,0.00004889216,0.0000238581,0.00001948423],"domain_scores_gemma":[0.999797,0.00005634019,0.00008443569,0.000009125744,0.00001599116,0.00003713362],"domain_codex":null,"domain_gemma":null,"domain_candidate":null,"domain_consensus":null,"study_design_codex":"case_report","study_design_gemma":"observational","study_design_scores_codex":[0.001035985,0.0001090254,0.1407059,0.0004154546,0.0001845945,0.6978585,0.000502645,0.0009990007,0.1376952,0.002461117,0.001297132,0.01673554],"study_design_scores_gemma":[0.0001496812,0.0005026276,0.1075645,0.0001158448,0.0003018596,0.8586802,0.0002774455,0.002400149,0.0229912,0.002336423,0.004641595,0.00003846012],"study_design_candidate":"observational","study_design_consensus":null,"genre_codex":"empirical","genre_gemma":"empirical","genre_scores_codex":[0.9926255,0.002323038,0.00197502,0.0003146571,0.00003120891,0.00001658926,0.000209852,0.0001101974,0.002393896],"genre_scores_gemma":[0.9983755,0.0004508933,0.0006861616,0.00004411965,0.00003037799,0.00000389879,0.0001248934,0.000008625592,0.0002755633],"genre_candidate":"empirical","genre_consensus":"empirical","teacher_disagreement_score":0.002895891,"threshold_uncertainty_score":0.009687722,"prediction_status":"machine_predicted_unvalidated"},"labels":[],"label_agreement":null},{"id":"W2139133783","doi":"10.1186/1471-2350-8-80","title":"Association between the -455T&gt;C promoter polymorphism of the APOC3gene and the metabolic syndrome in a multi-ethnic sample","year":2007,"lang":"en","type":"article","venue":"BMC Medical Genetics","topic":"Diabetes, Cardiovascular Risks, and Lipoproteins","field":"Medicine","cited_by":46,"is_retracted":false,"has_abstract":true,"routes":{"ca_aff":true,"ca_fund":true,"ca_venue":false,"about_ca":false},"ca_institutions":"St. Michael's Hospital; Western University; Lunenfeld-Tanenbaum Research Institute; Mount Sinai Hospital; McMaster University; University of Toronto; Hamilton Health Sciences; Robarts Clinical Trials; Population Health Research Institute; Public Health Ontario","funders":"Ontario Genomics; Ontario Genomics Institute; Genome Canada; Heart and Stroke Foundation of Canada","keywords":"Hypertriglyceridemia; Metabolic syndrome; Genetics; Genotype; Obesity; Internal medicine; Biology; Population; Odds ratio; Endocrinology; Medicine; Cholesterol; Gene; Triglyceride; Environmental health","authors":[{"name":"Rebecca L. Pollex","is_ca":true},{"name":"Matthew R. Ban","is_ca":true},{"name":"T. Kue Young","is_ca":true},{"name":"Peter Bjerregaard","is_ca":false},{"name":"Sonia S. Anand","is_ca":true},{"name":"Salim Yusuf","is_ca":true},{"name":"Bernard Zinman","is_ca":true},{"name":"Stewart B. Harris","is_ca":true},{"name":"Anthony J. Hanley","is_ca":true},{"name":"Philip W. Connelly","is_ca":true},{"name":"Murray W. Huff","is_ca":true},{"name":"Robert A. Hegele","is_ca":true}],"retraction":null,"screen_n_in":null,"score":{"opus":0.03188076227707666,"gpt":0.2828772740340028,"spread":0.2509965117569261,"validation_status":"score_only:v0-immature-baseline"},"prediction":{"model_version":"metacan-v3-hybrid-931329e0061c","candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0005656069,0.0004408468,0.000517763,0.0006683099,0.0006087071,0.0005437559,0.0003452914,0.0005090517,0.001788083],"category_scores_gemma":[0.001168986,0.0003657357,0.0004084074,0.0008436852,0.0002581762,0.0001936846,0.0003568648,0.0004709418,0.0002114506],"about_ca_system_candidate":false,"about_ca_system_consensus":false,"about_ca_system_score_codex":0.0001991822,"about_ca_system_score_gemma":0.0001683228,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_topic_score_codex":0.004947775,"about_ca_topic_score_gemma":0.005679985,"domain_scores_codex":[0.9995481,0.0001125297,0.0000538047,0.0001558333,0.00007879493,0.00005084725],"domain_scores_gemma":[0.999171,0.0001545937,0.0003222448,0.00007820773,0.00007817096,0.0001958568],"domain_codex":null,"domain_gemma":null,"domain_candidate":null,"domain_consensus":null,"study_design_codex":"observational","study_design_gemma":"observational","study_design_scores_codex":[0.0002867885,0.00004669396,0.9974965,0.000006891224,0.0001711614,0.0001568538,0.00007897538,0.00002254242,0.001059928,0.00000997395,0.00005450255,0.0006091136],"study_design_scores_gemma":[0.00001528735,0.00008327081,0.9990041,0.000003568544,0.00008060653,0.0004448265,0.00007361599,0.0001600435,0.00007077677,0.00001438348,0.00004651629,0.000002940335],"study_design_candidate":"observational","study_design_consensus":"observational","genre_codex":"empirical","genre_gemma":"empirical","genre_scores_codex":[0.9996603,0.0000889172,0.00005282216,0.0000154563,0.000003307795,0.000003579377,0.0001002331,0.000001523391,0.00007389957],"genre_scores_gemma":[0.9996027,0.0000432331,0.00009532327,0.00002306691,0.00000680534,0.000005740702,0.0001462971,0.000001836029,0.00007491413],"genre_candidate":"empirical","genre_consensus":"empirical","teacher_disagreement_score":0.004947775,"threshold_uncertainty_score":0.009837985,"prediction_status":"machine_predicted_unvalidated"},"labels":[],"label_agreement":null},{"id":"W1960333691","doi":"10.1186/s12881-015-0246-2","title":"Validation of a high resolution NGS method for detecting spinal muscular atrophy carriers among phase 3 participants in the 1000 Genomes Project","year":2015,"lang":"en","type":"article","venue":"BMC Medical Genetics","topic":"Neurogenetic and Muscular Disorders Research","field":"Medicine","cited_by":46,"is_retracted":false,"has_abstract":true,"routes":{"ca_aff":true,"ca_fund":false,"ca_venue":false,"about_ca":false},"ca_institutions":"Lockheed Martin (Canada)","funders":"","keywords":"SMN1; Spinal muscular atrophy; SMA*; Genetics; Biology; Carrier testing; Population; 1000 Genomes Project; Exome; Concordance; Bioinformatics; Computational biology; Exome sequencing; Gene; Computer science; Medicine; Single-nucleotide polymorphism; Prenatal diagnosis; Mutation; Algorithm","authors":[{"name":"Jessica L. Larson","is_ca":false},{"name":"Ari Silver","is_ca":true},{"name":"Dalin Chan","is_ca":false},{"name":"Carlos Borroto","is_ca":false},{"name":"Brett Spurrier","is_ca":true},{"name":"Lee M. Silver","is_ca":true}],"retraction":null,"screen_n_in":null,"score":{"opus":0.1257292477287624,"gpt":0.428206608161589,"spread":0.3024773604328266,"validation_status":"score_only:v0-immature-baseline"},"prediction":{"model_version":"metacan-v3-hybrid-931329e0061c","candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.02450646,0.0008240835,0.0005267953,0.001429556,0.0007051982,0.0008555281,0.001444535,0.001843041,0.001831006],"category_scores_gemma":[0.04563117,0.0005837454,0.001112773,0.0008313769,0.0007436547,0.0004507322,0.001397561,0.001010002,0.0007257399],"about_ca_system_candidate":false,"about_ca_system_consensus":false,"about_ca_system_score_codex":0.0004805005,"about_ca_system_score_gemma":0.001315707,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_topic_score_codex":0.004608614,"about_ca_topic_score_gemma":0.007049686,"domain_scores_codex":[0.9872754,0.007931062,0.0006236945,0.002140789,0.001825542,0.0002036187],"domain_scores_gemma":[0.9810655,0.01342975,0.001349772,0.002170365,0.001616012,0.000368672],"domain_codex":null,"domain_gemma":null,"domain_candidate":null,"domain_consensus":null,"study_design_codex":"observational","study_design_gemma":"bench_or_experimental","study_design_scores_codex":[0.002302569,0.0008121257,0.6564304,0.0007364227,0.002782261,0.0004962153,0.001434952,0.09209872,0.1001727,0.005655675,0.006555698,0.1305223],"study_design_scores_gemma":[0.0008000591,0.001407042,0.3829782,0.0001807437,0.0007859269,0.001436949,0.0003294249,0.5352046,0.05851224,0.007700928,0.01042494,0.000238993],"study_design_candidate":"bench_or_experimental","study_design_consensus":null,"genre_codex":"empirical","genre_gemma":"empirical","genre_scores_codex":[0.6226045,0.0004643687,0.3617177,0.0005679064,0.00009515944,0.0014802,0.009536605,0.001720372,0.001813165],"genre_scores_gemma":[0.6403535,0.0001124684,0.3470643,0.0004512611,0.00002925239,0.001747225,0.00921038,0.0002476624,0.0007839017],"genre_candidate":"empirical","genre_consensus":"empirical","teacher_disagreement_score":0.02450646,"threshold_uncertainty_score":0.1296041,"prediction_status":"machine_predicted_unvalidated"},"labels":[],"label_agreement":null},{"id":"W2068526813","doi":"10.1186/1471-2350-12-156","title":"Meta-analysis of 8q24 for seven cancers reveals a locus between NOV and ENPP2 associated with cancer development","year":2011,"lang":"en","type":"review","venue":"BMC Medical Genetics","topic":"Genetic factors in colorectal cancer","field":"Medicine","cited_by":44,"is_retracted":false,"has_abstract":true,"routes":{"ca_aff":true,"ca_fund":false,"ca_venue":false,"about_ca":false},"ca_institutions":"Lunenfeld-Tanenbaum Research Institute; Mount Sinai Hospital","funders":"National Institute of Neurological Disorders and Stroke; National Institute of General Medical Sciences; National Cancer Institute; National Institutes of Health; Mayo Foundation for Medical Education and Research","keywords":"Biology; Locus (genetics); Genome-wide association study; Single-nucleotide polymorphism; Pancreatic cancer; Chromosomal region; Breast cancer; Prostate cancer; Genetics; Colorectal cancer; Cancer; Oncogene; Quantitative trait locus; Human genetics; Gene; Genetic association; Internal medicine; Oncology; Genotype; Medicine; Cell cycle","authors":[{"name":"Abra Brisbin","is_ca":false},{"name":"Yan W. Asmann","is_ca":false},{"name":"Honglin Song","is_ca":false},{"name":"Ya-Yu Tsai","is_ca":false},{"name":"Jeremiah A. Aakre","is_ca":false},{"name":"Ping Yang","is_ca":false},{"name":"Robert B. Jenkins","is_ca":false},{"name":"Paul D.P. Pharoah","is_ca":false},{"name":"Fredrick R. Schumacher","is_ca":false},{"name":"David V. Conti","is_ca":false},{"name":"David Duggan","is_ca":false},{"name":"Mark A. Jenkins","is_ca":false},{"name":"John L. Hopper","is_ca":false},{"name":"Steven Gallinger","is_ca":true},{"name":"Polly A. Newcomb","is_ca":false},{"name":"Graham Casey","is_ca":false},{"name":"Thomas A. Sellers","is_ca":false},{"name":"Brooke L. Fridley","is_ca":false}],"retraction":null,"screen_n_in":null,"score":{"opus":0.3320764006322164,"gpt":0.4095648102942855,"spread":0.0774884096620691,"validation_status":"score_only:v0-immature-baseline"},"prediction":{"model_version":"metacan-v3-hybrid-931329e0061c","candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.006673336,0.001859747,0.003433741,0.003117409,0.0009499586,0.002096427,0.001323901,0.001451134,0.002635545],"category_scores_gemma":[0.01168658,0.0008578573,0.01872618,0.005214629,0.0005522331,0.0007595453,0.001590139,0.001614469,0.0002289826],"about_ca_system_candidate":false,"about_ca_system_consensus":false,"about_ca_system_score_codex":0.0006735813,"about_ca_system_score_gemma":0.0008405093,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_topic_score_codex":0.005977802,"about_ca_topic_score_gemma":0.01099281,"domain_scores_codex":[0.9942939,0.002210947,0.0007216707,0.001776269,0.000619377,0.0003777006],"domain_scores_gemma":[0.9904186,0.006279997,0.001140701,0.001245291,0.0005528664,0.0003625456],"domain_codex":null,"domain_gemma":null,"domain_candidate":null,"domain_consensus":null,"study_design_codex":"observational","study_design_gemma":"meta_analysis","study_design_scores_codex":[0.00453162,0.00003659123,0.5534019,0.004291761,0.4142928,0.001059396,0.0001385569,0.00214525,0.006288792,0.0003474256,0.001460132,0.01200578],"study_design_scores_gemma":[0.00050076,0.0005005523,0.4538122,0.0008408643,0.5326445,0.001330004,0.0002299991,0.002889267,0.001940127,0.00109238,0.004162894,0.00005657136],"study_design_candidate":"meta_analysis","study_design_consensus":null,"genre_codex":"empirical","genre_gemma":"review","genre_scores_codex":[0.6300749,0.3460506,0.01235834,0.002113121,0.0007109694,0.00009878098,0.005869055,0.0004168305,0.002307217],"genre_scores_gemma":[0.9845627,0.01122149,0.001962263,0.0003600707,0.0001249732,0.0000577561,0.001312379,0.00007209728,0.0003262972],"genre_candidate":"review","genre_consensus":null,"teacher_disagreement_score":0.006673336,"threshold_uncertainty_score":0.03529239,"prediction_status":"machine_predicted_unvalidated"},"labels":[],"label_agreement":null},{"id":"W2000256578","doi":"10.1186/1471-2350-13-72","title":"A founder mutation in the PEX6 gene is responsible for increased incidence of Zellweger syndrome in a French Canadian population","year":2012,"lang":"en","type":"article","venue":"BMC Medical Genetics","topic":"Peroxisome Proliferator-Activated Receptors","field":"Biochemistry, Genetics and Molecular Biology","cited_by":41,"is_retracted":false,"has_abstract":true,"routes":{"ca_aff":true,"ca_fund":true,"ca_venue":false,"about_ca":true},"ca_institutions":"McGill University; McGill University and Génome Québec Innovation Centre; Cégep de Chicoutimi; Université de Sherbrooke","funders":"Canadian Institutes of Health Research; National Institutes of Health; Université de Sherbrooke; National Institute of Neurological Disorders and Stroke; National Institute of General Medical Sciences; McGill University","keywords":"Biology; Genetics; Founder effect; Zellweger syndrome; Mutation; Population; Exon; Incidence (geometry); Peroxisomal disorder; Gene; Haplotype; Peroxisome; Allele; Medicine","authors":[{"name":"Sébastien Lévesque","is_ca":true},{"name":"Charles Morin","is_ca":true},{"name":"Simon‐Pierre Guay","is_ca":true},{"name":"Josée Villeneuve","is_ca":true},{"name":"Pascale Marquis","is_ca":true},{"name":"Wing Yik","is_ca":false},{"name":"Sarn Jiralerspong","is_ca":true},{"name":"Luigi Bouchard","is_ca":true},{"name":"Steven J. Steinberg","is_ca":false},{"name":"Joseph G. Hacia","is_ca":false},{"name":"Ken Dewar","is_ca":true},{"name":"Nancy Braverman","is_ca":true}],"retraction":null,"screen_n_in":null,"score":{"opus":0.01937086616183116,"gpt":0.2876466757186907,"spread":0.2682758095568596,"validation_status":"score_only:v0-immature-baseline"},"prediction":{"model_version":"metacan-v3-hybrid-931329e0061c","candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0003638524,0.0006517529,0.0003820536,0.00261458,0.002662901,0.0005652981,0.0008244817,0.0006135833,0.00618324],"category_scores_gemma":[0.001199221,0.000192487,0.0005174043,0.002292545,0.0006361715,0.0001555291,0.0004111383,0.0004745527,0.0002820577],"about_ca_system_candidate":false,"about_ca_system_consensus":false,"about_ca_system_score_codex":0.005533533,"about_ca_system_score_gemma":0.006084479,"about_ca_topic_candidate":true,"about_ca_topic_consensus":true,"about_ca_topic_score_codex":0.933404,"about_ca_topic_score_gemma":0.9143475,"domain_scores_codex":[0.9995905,0.00002749044,0.0000205747,0.00009739962,0.0001433659,0.0001206567],"domain_scores_gemma":[0.9993683,0.00006757189,0.0001243167,0.00002492687,0.000271532,0.0001434329],"domain_codex":null,"domain_gemma":null,"domain_candidate":null,"domain_consensus":null,"study_design_codex":"observational","study_design_gemma":"observational","study_design_scores_codex":[0.0002220179,0.00004028632,0.9671869,0.00006603872,0.0001188313,0.005555498,0.001090992,0.0003094141,0.004319674,0.0004015617,0.002064636,0.01862414],"study_design_scores_gemma":[0.00002408648,0.00008321307,0.9805796,0.00005537537,0.0001280183,0.01264093,0.001305008,0.0007580319,0.000524842,0.0001207887,0.003734473,0.00004573052],"study_design_candidate":"observational","study_design_consensus":"observational","genre_codex":"empirical","genre_gemma":"empirical","genre_scores_codex":[0.9941739,0.0009530506,0.0003518476,0.0003164426,0.00002232491,0.00002035073,0.0009832151,0.00004450449,0.003134345],"genre_scores_gemma":[0.9981157,0.0004078446,0.000342358,0.00006280086,0.000008586075,0.000004295247,0.0003247424,0.000007161896,0.000726461],"genre_candidate":"empirical","genre_consensus":"empirical","teacher_disagreement_score":0.06659603,"threshold_uncertainty_score":0.1339764,"prediction_status":"machine_predicted_unvalidated"},"labels":[],"label_agreement":null},{"id":"W1967054787","doi":"10.1186/s12881-014-0109-2","title":"CYP1B1 mutations in patients with primary congenital glaucoma from Saudi Arabia","year":2014,"lang":"en","type":"article","venue":"BMC Medical Genetics","topic":"Glaucoma and retinal disorders","field":"Medicine","cited_by":41,"is_retracted":false,"has_abstract":true,"routes":{"ca_aff":true,"ca_fund":false,"ca_venue":false,"about_ca":false},"ca_institutions":"McGill University; McGill University Health Centre","funders":"King Abdulaziz University","keywords":"Exon; CYP1B1; Allele; Compound heterozygosity; Genetics; Biology; Allele frequency; Genotype; Gene; Medicine; Internal medicine","authors":[{"name":"Osama Badeeb","is_ca":false},{"name":"Shazia Micheal","is_ca":false},{"name":"Robert K. Koenekoop","is_ca":true},{"name":"Anneke I. den Hollander","is_ca":false},{"name":"Manal Hedrawi","is_ca":false}],"retraction":null,"screen_n_in":null,"score":{"opus":0.00722332272159736,"gpt":0.2245337664552085,"spread":0.2173104437336111,"validation_status":"score_only:v0-immature-baseline"},"prediction":{"model_version":"metacan-v3-hybrid-931329e0061c","candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0001920024,0.0006701771,0.0003656045,0.001088695,0.0007382206,0.0003811945,0.0002949135,0.0006300011,0.003019604],"category_scores_gemma":[0.0009424827,0.000246289,0.000303887,0.0007319636,0.0003103997,0.0002101733,0.0004203217,0.0003084727,0.0003192913],"about_ca_system_candidate":false,"about_ca_system_consensus":false,"about_ca_system_score_codex":0.0003636222,"about_ca_system_score_gemma":0.0002934442,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_topic_score_codex":0.004478609,"about_ca_topic_score_gemma":0.003376929,"domain_scores_codex":[0.9997755,0.00002688596,0.000033563,0.00005921614,0.00004831998,0.00005655107],"domain_scores_gemma":[0.9995529,0.00008051501,0.0001907742,0.00002090163,0.00005596106,0.00009884156],"domain_codex":null,"domain_gemma":null,"domain_candidate":null,"domain_consensus":null,"study_design_codex":"observational","study_design_gemma":"observational","study_design_scores_codex":[0.0003446482,0.00006544476,0.9424174,0.00008882977,0.00004677367,0.04487993,0.0007735009,0.00007505312,0.004320694,0.00007866632,0.0005243266,0.006384771],"study_design_scores_gemma":[0.00007346588,0.0002905352,0.8022085,0.00007027722,0.00009117238,0.1940134,0.0008608788,0.0003119786,0.0008407897,0.0001010441,0.00112133,0.00001658273],"study_design_candidate":"observational","study_design_consensus":"observational","genre_codex":"empirical","genre_gemma":"empirical","genre_scores_codex":[0.9989932,0.0004133865,0.00004067256,0.00005913467,0.000008363261,0.000008420442,0.00009385137,0.000003891748,0.0003790105],"genre_scores_gemma":[0.9994924,0.0001879623,0.00007019789,0.00004467287,0.00001435378,0.000003119815,0.0001048343,0.000001340757,0.00008116691],"genre_candidate":"empirical","genre_consensus":"empirical","teacher_disagreement_score":0.004478609,"threshold_uncertainty_score":0.01010156,"prediction_status":"machine_predicted_unvalidated"},"labels":[],"label_agreement":null},{"id":"W1891364196","doi":"10.1186/1471-2350-4-7","title":"Founder mutations in BRCA1/2 are not frequent in Canadian Ashkenazi Jewish men with prostate cancer","year":2003,"lang":"en","type":"article","venue":"BMC Medical Genetics","topic":"BRCA gene mutations in cancer","field":"Biochemistry, Genetics and Molecular Biology","cited_by":40,"is_retracted":false,"has_abstract":true,"routes":{"ca_aff":true,"ca_fund":true,"ca_venue":false,"about_ca":true},"ca_institutions":"McGill University Health Centre; Jewish General Hospital; McGill University","funders":"National Institutes of Health; McGill University; U.S. Department of Defense","keywords":"Prostate cancer; Cancer; Prostate; Population; Mutation; Germline mutation; Biology; Genetics; Medicine; Oncology; Internal medicine; Gene","authors":[{"name":"Nancy Hamel","is_ca":true},{"name":"K Kotar","is_ca":true},{"name":"William D. Foulkes","is_ca":true}],"retraction":null,"screen_n_in":null,"score":{"opus":0.01755773568033574,"gpt":0.2851564774321714,"spread":0.2675987417518356,"validation_status":"score_only:v0-immature-baseline"},"prediction":{"model_version":"metacan-v3-hybrid-931329e0061c","candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0006176058,0.0003528501,0.000432171,0.001902623,0.00264831,0.0008017791,0.0010422,0.000589905,0.00366403],"category_scores_gemma":[0.003089083,0.0003350207,0.0003533262,0.003033662,0.0007724528,0.0002309159,0.0004338963,0.0004135679,0.000288492],"about_ca_system_candidate":false,"about_ca_system_consensus":false,"about_ca_system_score_codex":0.003441456,"about_ca_system_score_gemma":0.005648437,"about_ca_topic_candidate":true,"about_ca_topic_consensus":true,"about_ca_topic_score_codex":0.8686116,"about_ca_topic_score_gemma":0.9283848,"domain_scores_codex":[0.9990494,0.00005980103,0.00005407526,0.0001426977,0.0004622778,0.000231727],"domain_scores_gemma":[0.9983143,0.0001683743,0.0005041969,0.0001041436,0.0006515533,0.0002573894],"domain_codex":null,"domain_gemma":null,"domain_candidate":null,"domain_consensus":null,"study_design_codex":"observational","study_design_gemma":"observational","study_design_scores_codex":[0.0001216522,0.00002202584,0.9936923,0.00003475566,0.00004182756,0.0003859766,0.0004724201,0.00003902675,0.0007304083,0.00005059002,0.0005245929,0.003884369],"study_design_scores_gemma":[0.00001004262,0.00002627274,0.997484,0.00001618709,0.00004197415,0.0008776899,0.0004516993,0.00008332938,0.0001412547,0.00002481075,0.000832835,0.000009891508],"study_design_candidate":"observational","study_design_consensus":"observational","genre_codex":"empirical","genre_gemma":"empirical","genre_scores_codex":[0.9963709,0.0008504216,0.00007152429,0.0001110472,0.00001309236,0.00001730456,0.0005365227,0.00001007202,0.002019225],"genre_scores_gemma":[0.9989911,0.0003030963,0.0001044056,0.0000515817,0.000006940517,0.000003686685,0.0002230397,0.000003662694,0.0003124838],"genre_candidate":"empirical","genre_consensus":"empirical","teacher_disagreement_score":0.1313884,"threshold_uncertainty_score":0.2643242,"prediction_status":"machine_predicted_unvalidated"},"labels":[],"label_agreement":null},{"id":"W2072594666","doi":"10.1186/1471-2350-14-47","title":"Genetic variants of MARCO are associated with susceptibility to pulmonary tuberculosis in a Gambian population","year":2013,"lang":"en","type":"article","venue":"BMC Medical Genetics","topic":"Immune Response and Inflammation","field":"Immunology and Microbiology","cited_by":40,"is_retracted":false,"has_abstract":true,"routes":{"ca_aff":true,"ca_fund":true,"ca_venue":false,"about_ca":false},"ca_institutions":"McMaster University Medical Centre; McMaster University","funders":"National Institute of Allergy and Infectious Diseases; Medical Research Council; National Institutes of Health; Wellcome Trust; McMaster University","keywords":"Tuberculosis; Mycobacterium tuberculosis; Scavenger receptor; Immunology; Biology; Single-nucleotide polymorphism; Population; Latent tuberculosis; Macrophage; Receptor; Gene; Genetics; Medicine; Pathology; Genotype; In vitro; Endocrinology","authors":[{"name":"Dawn M. E. Bowdish","is_ca":true},{"name":"Kaori Sakamoto","is_ca":false},{"name":"Nathan A. Lack","is_ca":false},{"name":"Philip C. Hill","is_ca":false},{"name":"Giorgio Sirugo","is_ca":false},{"name":"Melanie J. Newport","is_ca":false},{"name":"Siamon Gordon","is_ca":false},{"name":"Adrian V. S. Hill","is_ca":false},{"name":"Fredrick O Vannberg","is_ca":false}],"retraction":null,"screen_n_in":null,"score":{"opus":0.01172494202723687,"gpt":0.232065892423103,"spread":0.2203409503958662,"validation_status":"score_only:v0-immature-baseline"},"prediction":{"model_version":"metacan-v3-hybrid-931329e0061c","candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0003606301,0.000779209,0.0003382221,0.001160656,0.0008509735,0.0005405095,0.0003101947,0.0005044862,0.003030773],"category_scores_gemma":[0.0008210334,0.0003790691,0.0002000484,0.001024496,0.00048192,0.0001851728,0.0004043024,0.0003511059,0.0001781756],"about_ca_system_candidate":false,"about_ca_system_consensus":false,"about_ca_system_score_codex":0.0002409622,"about_ca_system_score_gemma":0.0002314974,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_topic_score_codex":0.01542137,"about_ca_topic_score_gemma":0.01516878,"domain_scores_codex":[0.9997972,0.00007083249,0.00001521872,0.00005099168,0.00003067043,0.00003508626],"domain_scores_gemma":[0.9997845,0.00004550583,0.00008502799,0.00001356482,0.00002040158,0.00005101512],"domain_codex":null,"domain_gemma":null,"domain_candidate":null,"domain_consensus":null,"study_design_codex":"observational","study_design_gemma":"observational","study_design_scores_codex":[0.0003911146,0.00008661733,0.9893238,0.00004206923,0.0000951015,0.001277474,0.001087936,0.00007953564,0.004872344,0.0001134921,0.0001442082,0.002486256],"study_design_scores_gemma":[0.00001770337,0.0001219176,0.9969907,0.00004183202,0.00006825507,0.001399956,0.0006328871,0.0002027518,0.0001321224,0.0000573225,0.0003287715,0.000005787004],"study_design_candidate":"observational","study_design_consensus":"observational","genre_codex":"empirical","genre_gemma":"empirical","genre_scores_codex":[0.9993299,0.0002041923,0.00005624244,0.00002703753,0.000002408691,0.000007330329,0.00006803135,0.000003019289,0.0003018926],"genre_scores_gemma":[0.9994169,0.0001426172,0.0001571155,0.00001750663,0.000003595429,0.00001017002,0.00007206421,0.000001706926,0.0001782032],"genre_candidate":"empirical","genre_consensus":"empirical","teacher_disagreement_score":0.01542137,"threshold_uncertainty_score":0.03066319,"prediction_status":"machine_predicted_unvalidated"},"labels":[],"label_agreement":null},{"id":"W3093121240","doi":"10.1186/s12881-020-01115-w","title":"Associations of NOD2 polymorphisms with Erysipelotrichaceae in stool of in healthy first degree relatives of Crohn’s disease subjects","year":2020,"lang":"en","type":"article","venue":"BMC Medical Genetics","topic":"Gut microbiota and health","field":"Biochemistry, Genetics and Molecular Biology","cited_by":40,"is_retracted":false,"has_abstract":true,"routes":{"ca_aff":true,"ca_fund":true,"ca_venue":false,"about_ca":false},"ca_institutions":"Hôpital Maisonneuve-Rosemont; University of Alberta; University of Calgary; McMaster University; Sinai Health System; Mount Sinai Hospital; Lunenfeld-Tanenbaum Research Institute; Hospital for Sick Children; Public Health Ontario; University of Toronto","funders":"Institute of Nutrition, Metabolism and Diabetes; Canada Research Chairs; Canadian Association of Gastroenterology; Crohn's and Colitis Canada; Biocodex Microbiota Foundation; Canadian Institutes of Health Research; Leona M. and Harry B. Helmsley Charitable Trust","keywords":"NOD2; Microbiome; Biology; Crohn's disease; Inflammatory bowel disease; Immunology; Genetics; Disease; Single-nucleotide polymorphism; Genotype; Gene; Immune system; Internal medicine; Medicine; Innate immune system","authors":[{"name":"Williams Turpin","is_ca":true},{"name":"Larbi Bedrani","is_ca":true},{"name":"Osvaldo Espin‐Garcia","is_ca":true},{"name":"Wei Xu","is_ca":true},{"name":"Mark S. Silverberg","is_ca":true},{"name":"Michelle I. Smith","is_ca":true},{"name":"Juan A. Raygoza Garay","is_ca":true},{"name":"Sun-Ho Lee","is_ca":true},{"name":"David S. Guttman","is_ca":true},{"name":"Anne M. Griffiths","is_ca":true},{"name":"Paul Moayyedi","is_ca":true},{"name":"Remo Panaccione","is_ca":true},{"name":"Hien Q. Huynh","is_ca":true},{"name":"Hillary Steinhart","is_ca":true},{"name":"Levinus A. Dieleman","is_ca":true},{"name":"Dan Turner","is_ca":false},{"name":"Maria Abreu","is_ca":false},{"name":"Paul L. Beck","is_ca":true},{"name":"Çharles N. Bernstein","is_ca":false},{"name":"Kenneth Croitoru","is_ca":true},{"name":"Brian G. Feagan","is_ca":false},{"name":"Kevan Jacobson","is_ca":false},{"name":"Gilaad G. Kaplan","is_ca":false},{"name":"Denis O. Krause","is_ca":false},{"name":"Karen Madsen","is_ca":false},{"name":"John K. Marshall","is_ca":false},{"name":"Ernest G. Seidman","is_ca":false},{"name":"Andy Stadnyk","is_ca":false},{"name":"A. Hillary Steinhart","is_ca":true},{"name":"Michael G. Surette","is_ca":false},{"name":"Bruce A. Vallance","is_ca":false},{"name":"Alain Bitton","is_ca":false},{"name":"Maria Cino","is_ca":false},{"name":"Jeff Critch","is_ca":false},{"name":"Lee A. Denson","is_ca":true},{"name":"Colette Deslandres","is_ca":false},{"name":"Wael El‐Matary","is_ca":false},{"name":"Hans Herfarth","is_ca":false},{"name":"Peter Higgins","is_ca":false},{"name":"Jeff Hyams","is_ca":true},{"name":"David Mack","is_ca":false},{"name":"Jerry McGrath","is_ca":false},{"name":"Anthony Otley","is_ca":true},{"name":"Remo Panancionne","is_ca":false},{"name":"Robert N. Baldassano","is_ca":true},{"name":"Charlotte Hedin","is_ca":false},{"name":"Séamus Hussey","is_ca":true},{"name":"Hien Hyams","is_ca":true},{"name":"David J. Keljo","is_ca":true},{"name":"David Kevans","is_ca":false},{"name":"Charlie W. Lees","is_ca":false},{"name":"Sanjay K. Murthy","is_ca":true},{"name":"Nimisha Parekh","is_ca":false},{"name":"Sophie Plamondon","is_ca":false},{"name":"Graham Radford-Smith","is_ca":true},{"name":"Mark J. Ropeleski","is_ca":false},{"name":"Joel R. Rosh","is_ca":true},{"name":"David T. Rubin","is_ca":false},{"name":"Michael Schultz","is_ca":false},{"name":"Corey A. Siegel","is_ca":false},{"name":"Scott B. Snapper","is_ca":true},{"name":"Andrew D. Paterson","is_ca":true}],"retraction":null,"screen_n_in":null,"score":{"opus":0.04000012695744246,"gpt":0.2846364023111075,"spread":0.244636275353665,"validation_status":"score_only:v0-immature-baseline"},"prediction":{"model_version":"metacan-v3-hybrid-931329e0061c","candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.000257128,0.000449227,0.0004027336,0.0006528902,0.0004378231,0.0004134519,0.0001839471,0.0004786532,0.00197285],"category_scores_gemma":[0.001052526,0.0002597524,0.0004233826,0.0005854091,0.0002341497,0.0001945876,0.0003257056,0.0004236846,0.0002108332],"about_ca_system_candidate":false,"about_ca_system_consensus":false,"about_ca_system_score_codex":0.000178162,"about_ca_system_score_gemma":0.00009215589,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_topic_score_codex":0.00269564,"about_ca_topic_score_gemma":0.002373648,"domain_scores_codex":[0.9997413,0.00004374732,0.00003121611,0.0001130123,0.00002816604,0.00004263796],"domain_scores_gemma":[0.999448,0.0001024028,0.0002321551,0.00004858004,0.00004503945,0.0001237242],"domain_codex":null,"domain_gemma":null,"domain_candidate":null,"domain_consensus":null,"study_design_codex":"observational","study_design_gemma":"observational","study_design_scores_codex":[0.0008886536,0.0000695975,0.9917162,0.00003335422,0.0001424737,0.0007863527,0.0001692374,0.00004410368,0.004817895,0.00002191301,0.00007790099,0.001232213],"study_design_scores_gemma":[0.00001285562,0.0001832527,0.9977354,0.000008801905,0.00007148364,0.00125784,0.0001656277,0.0001027033,0.0003023325,0.00002563547,0.0001299329,0.00000413243],"study_design_candidate":"observational","study_design_consensus":"observational","genre_codex":"empirical","genre_gemma":"empirical","genre_scores_codex":[0.9995143,0.000189295,0.00005153485,0.00001032383,0.000004194753,0.000002020281,0.0001103406,0.000002122724,0.0001158555],"genre_scores_gemma":[0.9996814,0.00005419262,0.00005442719,0.000008951035,0.000003963386,0.000002257769,0.00009316685,0.000001528103,0.0001001435],"genre_candidate":"empirical","genre_consensus":"empirical","teacher_disagreement_score":0.00269564,"threshold_uncertainty_score":0.006599844,"prediction_status":"machine_predicted_unvalidated"},"labels":[],"label_agreement":null},{"id":"W1835707115","doi":"10.1186/s12881-015-0180-3","title":"Molecular and clinical study of a cohort of 110 Algerian patients with autosomal recessive ataxia","year":2015,"lang":"en","type":"article","venue":"BMC Medical Genetics","topic":"Genetic Neurodegenerative Diseases","field":"Neuroscience","cited_by":39,"is_retracted":false,"has_abstract":true,"routes":{"ca_aff":false,"ca_fund":false,"ca_venue":false,"about_ca":true},"ca_institutions":"","funders":"Centre National de la Recherche Scientifique; Ministère de la Santé; Ministère de l'Enseignement Supérieur et de la Recherche; Ministère de l'Enseignement Supérieur et de la Recherche Scientifique; E-Rare; Agence Nationale de la Recherche; Institut National de la Santé et de la Recherche Médicale","keywords":"Ataxia; Cerebellar ataxia; Genetics; Biology; Population; Genetic heterogeneity; Cohort; Phenotype; Spinocerebellar ataxia; Medicine; Gene; Pathology; Neuroscience","authors":[{"name":"Wahiba Hamza","is_ca":false},{"name":"Lamia Ali Pacha","is_ca":false},{"name":"Tarik Hamadouche","is_ca":false},{"name":"Jean Muller","is_ca":false},{"name":"Nathalie Drouot","is_ca":false},{"name":"Farida Ferrat","is_ca":false},{"name":"S. Makri","is_ca":false},{"name":"Malika Chaouch","is_ca":false},{"name":"Mériem Tazir","is_ca":false},{"name":"Michel Kœnig","is_ca":false},{"name":"Traki Benhassine","is_ca":false}],"retraction":null,"screen_n_in":null,"score":{"opus":0.0451978740766313,"gpt":0.3250538826605019,"spread":0.2798560085838707,"validation_status":"score_only:v0-immature-baseline"},"prediction":{"model_version":"metacan-v3-hybrid-931329e0061c","candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0002256305,0.0006234207,0.0004474216,0.00127009,0.0009107179,0.000626252,0.0003621032,0.0003923583,0.001705198],"category_scores_gemma":[0.001061494,0.0003485876,0.000254787,0.0008567472,0.0003970206,0.0002651107,0.000460429,0.0002462446,0.000320348],"about_ca_system_candidate":false,"about_ca_system_consensus":false,"about_ca_system_score_codex":0.0006001044,"about_ca_system_score_gemma":0.0003411264,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_topic_score_codex":0.008743561,"about_ca_topic_score_gemma":0.00498344,"domain_scores_codex":[0.9997452,0.00002960262,0.00002501151,0.0001101094,0.00004176996,0.00004833377],"domain_scores_gemma":[0.9996296,0.00006263782,0.0001192571,0.00003207436,0.00006395944,0.00009239067],"domain_codex":null,"domain_gemma":null,"domain_candidate":null,"domain_consensus":null,"study_design_codex":"observational","study_design_gemma":"observational","study_design_scores_codex":[0.0001919158,0.00009481276,0.9887913,0.00002521111,0.00004350384,0.004269713,0.0008601514,0.00007786784,0.002470499,0.00003853066,0.0001902694,0.002946263],"study_design_scores_gemma":[0.00001704273,0.0001905103,0.9885694,0.00001316426,0.00003594429,0.00946123,0.0005955644,0.0001263148,0.0002765286,0.00002389788,0.0006825716,0.000007794363],"study_design_candidate":"observational","study_design_consensus":"observational","genre_codex":"empirical","genre_gemma":"empirical","genre_scores_codex":[0.9995602,0.00007657945,0.00003370561,0.00001098401,0.000001794112,0.000009733181,0.000142401,0.00000186485,0.0001627118],"genre_scores_gemma":[0.9989886,0.0001259267,0.0001128036,0.00003063808,0.000006556735,0.00001697078,0.0004851152,0.000002548844,0.0002308179],"genre_candidate":"empirical","genre_consensus":"empirical","teacher_disagreement_score":0.008743561,"threshold_uncertainty_score":0.0173853,"prediction_status":"machine_predicted_unvalidated"},"labels":[],"label_agreement":null},{"id":"W2167219284","doi":"10.1186/s12881-014-0120-7","title":"A study of genes encoding cytokines (IL6, IL10, TNF), cytokine receptors (IL6R, IL6ST), and glucocorticoid receptor (NR3C1) and susceptibility to bronchopulmonary dysplasia","year":2014,"lang":"en","type":"article","venue":"BMC Medical Genetics","topic":"Neonatal Respiratory Health Research","field":"Medicine","cited_by":38,"is_retracted":false,"has_abstract":true,"routes":{"ca_aff":true,"ca_fund":true,"ca_venue":false,"about_ca":true},"ca_institutions":"Child and Family Research Institute","funders":"Tays; Oulun Yliopisto; Emil Aaltosen Säätiö; Academy of Finland; Helsingin Yliopisto; Kuopion Yliopistollinen Sairaala; Helsingin ja Uudenmaan Sairaanhoitopiiri; Michael Smith Health Research BC; University of Ottawa; British Columbia Lung Association; Turun Yliopistollinen Keskussairaala; Stiftelsen Alma och K. A. Snellman Säätiö","keywords":"Single-nucleotide polymorphism; Biology; Immunology; Glucocorticoid receptor; Bronchopulmonary dysplasia; Internal medicine; Glucocorticoid; Genetics; Medicine; Genotype; Gene; Pregnancy","authors":[{"name":"Johanna M. Huusko","is_ca":false},{"name":"Minna K. Karjalainen","is_ca":false},{"name":"Mari Mahlman","is_ca":false},{"name":"Ritva Haataja","is_ca":false},{"name":"M. Anneli Kari","is_ca":false},{"name":"Sture Andersson","is_ca":false},{"name":"Gergely Toldi","is_ca":false},{"name":"Outi Tammela","is_ca":false},{"name":"Mika Rämet","is_ca":false},{"name":"Pascal M. Lavoie","is_ca":true},{"name":"Mikko Hallman","is_ca":false}],"retraction":null,"screen_n_in":null,"score":{"opus":0.04776766476752504,"gpt":0.353695770172386,"spread":0.3059281054048609,"validation_status":"score_only:v0-immature-baseline"},"prediction":{"model_version":"metacan-v3-hybrid-931329e0061c","candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0003402689,0.0004021059,0.0002514429,0.0005121544,0.0003877429,0.0002191518,0.0002234336,0.0003648924,0.001170676],"category_scores_gemma":[0.0008931137,0.000117316,0.0003830602,0.0006630591,0.0002572224,0.00007812005,0.0001717133,0.0002866622,0.0001425952],"about_ca_system_candidate":false,"about_ca_system_consensus":false,"about_ca_system_score_codex":0.000294203,"about_ca_system_score_gemma":0.0004306154,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_topic_score_codex":0.01179119,"about_ca_topic_score_gemma":0.007551893,"domain_scores_codex":[0.9997194,0.00006752869,0.00001868259,0.0001082824,0.00005194464,0.00003409372],"domain_scores_gemma":[0.9993808,0.000208626,0.0001721618,0.00003985739,0.00006991548,0.0001286238],"domain_codex":null,"domain_gemma":null,"domain_candidate":null,"domain_consensus":null,"study_design_codex":"observational","study_design_gemma":"observational","study_design_scores_codex":[0.001182695,0.00009543658,0.9565693,0.00008432069,0.0003954199,0.001402353,0.0003932821,0.0001547196,0.03149614,0.00007213968,0.0001641349,0.007990154],"study_design_scores_gemma":[0.00003835046,0.0003061891,0.9953228,0.00001284492,0.0001434012,0.001826517,0.0001103565,0.0001975959,0.001460377,0.0000321694,0.0005444525,0.000004914315],"study_design_candidate":"observational","study_design_consensus":"observational","genre_codex":"empirical","genre_gemma":"empirical","genre_scores_codex":[0.9989055,0.0005019412,0.0002344062,0.00003346051,0.00000433215,0.000006778901,0.0001603175,0.000003122301,0.0001501527],"genre_scores_gemma":[0.9987245,0.0001958589,0.0005326868,0.00002572354,0.000007578062,0.00000813209,0.000228366,0.000001852508,0.0002752422],"genre_candidate":"empirical","genre_consensus":"empirical","teacher_disagreement_score":0.01179119,"threshold_uncertainty_score":0.02344513,"prediction_status":"machine_predicted_unvalidated"},"labels":[],"label_agreement":null},{"id":"W1509071637","doi":"10.1186/1471-2350-5-24","title":"Characterization of a new full length TMPRSS3 isoform and identification of mutant alleles responsible for nonsyndromic recessive deafness in Newfoundland and Pakistan","year":2004,"lang":"en","type":"article","venue":"BMC Medical Genetics","topic":"Hearing, Cochlea, Tinnitus, Genetics","field":"Neuroscience","cited_by":37,"is_retracted":false,"has_abstract":true,"routes":{"ca_aff":true,"ca_fund":false,"ca_venue":false,"about_ca":true},"ca_institutions":"Alberta Children's Hospital; Memorial University of Newfoundland","funders":"National Institute on Deafness and Other Communication Disorders; National Institutes of Health; International Centre for Genetic Engineering and Biotechnology","keywords":"Genetics; Biology; Allele; Locus (genetics); Genotype; Exon; Context (archaeology); Mutant; Gene","authors":[{"name":"Zubair M. Ahmed","is_ca":false},{"name":"Xiaoyan Cindy Li","is_ca":false},{"name":"Shontell D Powell","is_ca":false},{"name":"Saima Riazuddin","is_ca":false},{"name":"Terry‐Lynn Young","is_ca":true},{"name":"Khushnooda Ramzan","is_ca":false},{"name":"Zahoor Ahmad","is_ca":false},{"name":"Sandra Luscombe","is_ca":true},{"name":"Kiran Dhillon","is_ca":false},{"name":"Linda MacLaren","is_ca":true},{"name":"Barbara Ploplis","is_ca":false},{"name":"Lawrence I. Shotland","is_ca":false},{"name":"Elizabeth Ives","is_ca":true},{"name":"Sheikh Riazuddin","is_ca":false},{"name":"Thomas B. Friedman","is_ca":false},{"name":"Robert J. Morell","is_ca":false},{"name":"Edward R. Wilcox","is_ca":false}],"retraction":null,"screen_n_in":null,"score":{"opus":0.03860492765939572,"gpt":0.3185398907187062,"spread":0.2799349630593105,"validation_status":"score_only:v0-immature-baseline"},"prediction":{"model_version":"metacan-v3-hybrid-931329e0061c","candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00006367053,0.0002702129,0.0001330191,0.0004139065,0.0002860618,0.0001682196,0.0001667583,0.0001862684,0.001049196],"category_scores_gemma":[0.0001647122,0.0001078502,0.0002167159,0.0003205246,0.0002654448,0.00007226288,0.0001524742,0.0002022839,0.0001989616],"about_ca_system_candidate":false,"about_ca_system_consensus":false,"about_ca_system_score_codex":0.0006452752,"about_ca_system_score_gemma":0.000450331,"about_ca_topic_candidate":true,"about_ca_topic_consensus":false,"about_ca_topic_score_codex":0.03455314,"about_ca_topic_score_gemma":0.04610057,"domain_scores_codex":[0.9999311,0.000003103932,0.000006851408,0.00001801721,0.00001849372,0.00002253382],"domain_scores_gemma":[0.9998775,0.00002062726,0.00004172551,0.000006395453,0.00002317304,0.00003067894],"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":[0.0005592972,0.00008429015,0.1519709,0.00007737718,0.00004896209,0.01421366,0.0007445027,0.0002508515,0.8213399,0.0001437127,0.0003313584,0.01023524],"study_design_scores_gemma":[0.00003907885,0.0002815669,0.9363273,0.00001509132,0.0000569314,0.02008852,0.0006214688,0.0005715185,0.03937578,0.00004910354,0.002560138,0.0000135264],"study_design_candidate":"observational","study_design_consensus":null,"genre_codex":"empirical","genre_gemma":"empirical","genre_scores_codex":[0.9992732,0.00007165394,0.0001681165,0.00002261313,0.000002089567,0.000006072813,0.0002167585,0.000003569961,0.0002359112],"genre_scores_gemma":[0.9980668,0.000107411,0.00056289,0.0000275135,0.000002276539,0.000005636004,0.000581972,0.00000397699,0.0006415462],"genre_candidate":"empirical","genre_consensus":"empirical","teacher_disagreement_score":0.9654469,"threshold_uncertainty_score":0.06870401,"prediction_status":"machine_predicted_unvalidated"},"labels":[],"label_agreement":null},{"id":"W2090225469","doi":"10.1186/1471-2350-12-117","title":"Effect of heme oxygenase-1 polymorphisms on lung function and gene expression","year":2011,"lang":"en","type":"article","venue":"BMC Medical Genetics","topic":"Heme Oxygenase-1 and Carbon Monoxide","field":"Biochemistry, Genetics and Molecular Biology","cited_by":37,"is_retracted":false,"has_abstract":true,"routes":{"ca_aff":true,"ca_fund":true,"ca_venue":false,"about_ca":false},"ca_institutions":"Vancouver General Hospital; University of Manitoba; St. Paul's Hospital","funders":"National Heart, Lung, and Blood Institute; Canadian Institutes of Health Research; Killam Trusts; National Institutes of Health; Michael Smith Health Research BC","keywords":"HMOX1; Single-nucleotide polymorphism; Heme oxygenase; Biology; SNP; Oxidative stress; Heme; Gene expression; Linkage disequilibrium; Genetics; Gene; Molecular biology; Genotype; Endocrinology; Biochemistry; Enzyme","authors":[{"name":"Goh Tanaka","is_ca":true},{"name":"Farzian Aminuddin","is_ca":true},{"name":"Loubna Akhabir","is_ca":true},{"name":"Jian‐Qing He","is_ca":true},{"name":"Karey Shumansky","is_ca":true},{"name":"John E. Connett","is_ca":false},{"name":"Nicholas R. Anthonisen","is_ca":true},{"name":"Raja T. Abboud","is_ca":true},{"name":"Peter D. Paré","is_ca":true},{"name":"Andrew J. Sandford","is_ca":true}],"retraction":null,"screen_n_in":null,"score":{"opus":0.01169315375734313,"gpt":0.2416453498379049,"spread":0.2299521960805618,"validation_status":"score_only:v0-immature-baseline"},"prediction":{"model_version":"metacan-v3-hybrid-931329e0061c","candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0005447255,0.0002945699,0.0003199781,0.0002151241,0.0001488733,0.000240075,0.0001852469,0.0003456156,0.001558868],"category_scores_gemma":[0.0009323446,0.0001097427,0.0002444814,0.0003140102,0.0002635251,0.00008702161,0.0001329827,0.0003763187,0.0001537664],"about_ca_system_candidate":false,"about_ca_system_consensus":false,"about_ca_system_score_codex":0.0001451853,"about_ca_system_score_gemma":0.0001210638,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_topic_score_codex":0.001471531,"about_ca_topic_score_gemma":0.001011892,"domain_scores_codex":[0.9996579,0.0001200737,0.0000186553,0.0001128307,0.00004752217,0.00004297006],"domain_scores_gemma":[0.9989256,0.0006494276,0.000193254,0.0000743401,0.00005306751,0.0001042616],"domain_codex":null,"domain_gemma":null,"domain_candidate":null,"domain_consensus":null,"study_design_codex":"observational","study_design_gemma":"observational","study_design_scores_codex":[0.01025291,0.0003566194,0.8104141,0.00008983289,0.0007042499,0.0007946728,0.0002753346,0.0004945504,0.1684816,0.0001571698,0.0002871632,0.007691809],"study_design_scores_gemma":[0.00005233399,0.0006559885,0.9923891,0.000006735565,0.0001888176,0.0004672039,0.00003858767,0.00071638,0.00511504,0.00009365655,0.000271247,0.000004793205],"study_design_candidate":"observational","study_design_consensus":"observational","genre_codex":"empirical","genre_gemma":"empirical","genre_scores_codex":[0.9994026,0.0001745898,0.00011639,0.00003264972,0.000003614303,0.000002515566,0.0001234012,0.000003927515,0.0001402592],"genre_scores_gemma":[0.9994788,0.00003832988,0.0001456259,0.00002449479,0.000006113522,0.000006323921,0.0001086158,0.000004300251,0.0001875481],"genre_candidate":"empirical","genre_consensus":"empirical","teacher_disagreement_score":0.001558868,"threshold_uncertainty_score":0.00521493,"prediction_status":"machine_predicted_unvalidated"},"labels":[],"label_agreement":null},{"id":"W2063505762","doi":"10.1186/1471-2350-12-56","title":"A novel deletion mutation in the TUSC3 gene in a consanguineous Pakistani family with autosomal recessive nonsyndromic intellectual disability","year":2011,"lang":"en","type":"article","venue":"BMC Medical Genetics","topic":"Genetics and Neurodevelopmental Disorders","field":"Biochemistry, Genetics and Molecular Biology","cited_by":37,"is_retracted":false,"has_abstract":true,"routes":{"ca_aff":true,"ca_fund":true,"ca_venue":false,"about_ca":false},"ca_institutions":"University of Toronto; Centre for Addiction and Mental Health","funders":"Canadian Institutes of Health Research; National Alliance for Research on Schizophrenia and Depression","keywords":"Genetics; Biology; Locus (genetics); Gene; Disease gene identification; Human genetics; Genetic linkage; Consanguinity; Mutation; Exome sequencing","authors":[{"name":"Muzammil Ahmad Khan","is_ca":false},{"name":"Muhammad Rafiq","is_ca":true},{"name":"Abdul Noor","is_ca":true},{"name":"Nadir Ali","is_ca":false},{"name":"Ghazanfar Ali","is_ca":false},{"name":"John B. Vincent","is_ca":true},{"name":"Muhammad Ansar","is_ca":false}],"retraction":null,"screen_n_in":null,"score":{"opus":0.02569105730120841,"gpt":0.2523504601660443,"spread":0.2266594028648359,"validation_status":"score_only:v0-immature-baseline"},"prediction":{"model_version":"metacan-v3-hybrid-931329e0061c","candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0002215811,0.001166597,0.0005473961,0.001118333,0.0016272,0.0003415791,0.0006032268,0.001488301,0.003369309],"category_scores_gemma":[0.001194456,0.000294085,0.0004439515,0.000774092,0.001121635,0.0002693122,0.0005785078,0.000769682,0.000281153],"about_ca_system_candidate":false,"about_ca_system_consensus":false,"about_ca_system_score_codex":0.0005261668,"about_ca_system_score_gemma":0.0006340868,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_topic_score_codex":0.006887993,"about_ca_topic_score_gemma":0.006888509,"domain_scores_codex":[0.9997091,0.00002820341,0.00002349255,0.0001307263,0.00005490934,0.00005355191],"domain_scores_gemma":[0.9993717,0.0002796554,0.0001114992,0.00002854316,0.00004452024,0.0001640385],"domain_codex":null,"domain_gemma":null,"domain_candidate":null,"domain_consensus":null,"study_design_codex":"case_report","study_design_gemma":"case_report","study_design_scores_codex":[0.0002243365,0.0001062917,0.04058702,0.00005645504,0.00004354984,0.9371898,0.001013682,0.0001746638,0.01591526,0.0003857303,0.0005137053,0.003789534],"study_design_scores_gemma":[0.00005605878,0.0003242446,0.09539802,0.00003355534,0.00006941691,0.8979449,0.0004086278,0.0007025109,0.003455302,0.0003037143,0.001264672,0.00003890406],"study_design_candidate":"case_report","study_design_consensus":"case_report","genre_codex":"empirical","genre_gemma":"empirical","genre_scores_codex":[0.9970369,0.000351691,0.0007246758,0.0003137137,0.00004243362,0.00003695124,0.0002012443,0.00003408308,0.001258336],"genre_scores_gemma":[0.998965,0.00008128935,0.0003741018,0.0001008986,0.00002556434,0.000007194063,0.00005247704,0.000006481566,0.0003869649],"genre_candidate":"empirical","genre_consensus":"empirical","teacher_disagreement_score":0.006887993,"threshold_uncertainty_score":0.01369584,"prediction_status":"machine_predicted_unvalidated"},"labels":[],"label_agreement":null},{"id":"W2021119602","doi":"10.1186/1471-2350-10-30","title":"Knowledge about hereditary nonpolyposis colorectal cancer; mutation carriers and physicians at equal levels","year":2009,"lang":"en","type":"article","venue":"BMC Medical Genetics","topic":"Genetic factors in colorectal cancer","field":"Medicine","cited_by":33,"is_retracted":false,"has_abstract":true,"routes":{"ca_aff":false,"ca_fund":true,"ca_venue":false,"about_ca":false},"ca_institutions":"","funders":"University of Toronto; Lunds Universitet","keywords":"Medicine; Colorectal cancer; Genetic counseling; Heredity; Family medicine; Genetic testing; Cancer; Lynch syndrome; Human genetics; Oncology; Gynecology; Internal medicine; Genetics; DNA mismatch repair","authors":[{"name":"Katarina Domanska","is_ca":false},{"name":"Christina Carlsson","is_ca":false},{"name":"Pär‐Ola Bendahl","is_ca":false},{"name":"Mef Nilbert","is_ca":false}],"retraction":null,"screen_n_in":null,"score":{"opus":0.03244920221694034,"gpt":0.3274128581576131,"spread":0.2949636559406728,"validation_status":"score_only:v0-immature-baseline"},"prediction":{"model_version":"metacan-v3-hybrid-931329e0061c","candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.001689078,0.0001410444,0.0003013811,0.001356606,0.000530235,0.000689466,0.0002891107,0.0007823391,0.007220137],"category_scores_gemma":[0.01590828,0.0001449456,0.0001649854,0.0007633007,0.0005685,0.0009465556,0.0005237443,0.0005668357,0.0003962113],"about_ca_system_candidate":false,"about_ca_system_consensus":false,"about_ca_system_score_codex":0.000606063,"about_ca_system_score_gemma":0.0006619349,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_topic_score_codex":0.01248718,"about_ca_topic_score_gemma":0.006426766,"domain_scores_codex":[0.9986112,0.0005365562,0.0001032557,0.0001339231,0.0003772778,0.0002378713],"domain_scores_gemma":[0.9873508,0.006208197,0.003701732,0.000190598,0.0006302848,0.00191842],"domain_codex":null,"domain_gemma":null,"domain_candidate":null,"domain_consensus":null,"study_design_codex":"observational","study_design_gemma":"observational","study_design_scores_codex":[0.00008144905,0.0001231617,0.9892146,0.00004490526,0.0000274342,0.0003562473,0.003264794,0.00007488383,0.0001228276,0.00008854652,0.0005652399,0.006035858],"study_design_scores_gemma":[0.000008262554,0.0001307073,0.9943973,0.00006798164,0.00002091821,0.0009257188,0.003241895,0.0001788287,0.00004884808,0.0001373499,0.0008352301,0.000007009985],"study_design_candidate":"observational","study_design_consensus":"observational","genre_codex":"empirical","genre_gemma":"empirical","genre_scores_codex":[0.9952675,0.0009679724,0.00004988279,0.001215799,0.00001528638,0.00001074335,0.0001163316,0.000003392114,0.002353054],"genre_scores_gemma":[0.9992637,0.0002500853,0.00004007453,0.000139307,0.00001510342,0.00000432488,0.00005092808,6.604495e-7,0.0002357704],"genre_candidate":"empirical","genre_consensus":"empirical","teacher_disagreement_score":0.01248718,"threshold_uncertainty_score":0.02482897,"prediction_status":"machine_predicted_unvalidated"},"labels":[],"label_agreement":null},{"id":"W2099991149","doi":"10.1186/1471-2350-9-21","title":"Influence of leukotriene gene polymorphisms on chronic rhinosinusitis","year":2008,"lang":"en","type":"article","venue":"BMC Medical Genetics","topic":"Sinusitis and nasal conditions","field":"Medicine","cited_by":33,"is_retracted":false,"has_abstract":true,"routes":{"ca_aff":true,"ca_fund":true,"ca_venue":false,"about_ca":false},"ca_institutions":"Université de Montréal; Université Laval; Institut universitaire de cardiologie et de pneumologie de Québec; Ontario Institute for Cancer Research; McGill University and Génome Québec Innovation Centre; McGill University","funders":"Canadian Institutes of Health Research; McGill University; Burroughs Wellcome Fund","keywords":"Human genetics; Chronic rhinosinusitis; Genetics; Gene; Biology; Leukotriene; Computational biology; Immunology; Asthma","authors":[{"name":"Hasan Al-Shemari","is_ca":true},{"name":"Yohan Bossé","is_ca":true},{"name":"Thomas J. Hudson","is_ca":true},{"name":"Myrna Cabaluna","is_ca":true},{"name":"Mélanie Duval","is_ca":true},{"name":"Mathieu Lemire","is_ca":true},{"name":"Sophie Vallée‐Smedja","is_ca":true},{"name":"Saul Frenkiel","is_ca":true},{"name":"Martin Desrosiers","is_ca":true}],"retraction":null,"screen_n_in":null,"score":{"opus":0.02847403634547451,"gpt":0.2799229027657136,"spread":0.2514488664202391,"validation_status":"score_only:v0-immature-baseline"},"prediction":{"model_version":"metacan-v3-hybrid-931329e0061c","candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0007405645,0.000460692,0.0003600777,0.0004759825,0.0003856974,0.00039246,0.0002369075,0.000465625,0.002319739],"category_scores_gemma":[0.002129847,0.0001332578,0.0007678428,0.0005731437,0.0003035522,0.0001389685,0.0002575068,0.0003690342,0.0002047609],"about_ca_system_candidate":false,"about_ca_system_consensus":false,"about_ca_system_score_codex":0.0001882117,"about_ca_system_score_gemma":0.0002542555,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_topic_score_codex":0.003182361,"about_ca_topic_score_gemma":0.002482065,"domain_scores_codex":[0.9992238,0.0002559464,0.00007621233,0.0002253912,0.000129812,0.00008873567],"domain_scores_gemma":[0.998566,0.0007145373,0.0003460314,0.00009243797,0.00009677748,0.0001842486],"domain_codex":null,"domain_gemma":null,"domain_candidate":null,"domain_consensus":null,"study_design_codex":"observational","study_design_gemma":"observational","study_design_scores_codex":[0.002229177,0.00007903811,0.9739088,0.00005355872,0.0006253762,0.001088393,0.0001137521,0.0002699374,0.01658401,0.00007608934,0.0001064143,0.004865331],"study_design_scores_gemma":[0.00002150136,0.0002678118,0.9977008,0.000007876171,0.0002117014,0.0006980766,0.00004449534,0.0002591142,0.0005634135,0.00003943265,0.0001818502,0.000003945858],"study_design_candidate":"observational","study_design_consensus":"observational","genre_codex":"empirical","genre_gemma":"empirical","genre_scores_codex":[0.9990001,0.0003892745,0.0001611404,0.00002682755,0.000006330545,0.000004380358,0.0001652847,0.000004102807,0.0002425562],"genre_scores_gemma":[0.9996597,0.00005930575,0.0001061922,0.00001041107,0.000003902587,0.000003304731,0.00008853468,0.000002290276,0.00006641992],"genre_candidate":"empirical","genre_consensus":"empirical","teacher_disagreement_score":0.003182361,"threshold_uncertainty_score":0.007760346,"prediction_status":"machine_predicted_unvalidated"},"labels":[],"label_agreement":null},{"id":"W2030256476","doi":"10.1186/1471-2350-10-117","title":"Genetic variation in the NBS1, MRE11, RAD50 and BLM genes and susceptibility to non-Hodgkin lymphoma","year":2009,"lang":"en","type":"article","venue":"BMC Medical Genetics","topic":"Lymphoma Diagnosis and Treatment","field":"Medicine","cited_by":33,"is_retracted":false,"has_abstract":true,"routes":{"ca_aff":true,"ca_fund":true,"ca_venue":false,"about_ca":false},"ca_institutions":"Simon Fraser University; University of British Columbia; Canada's Michael Smith Genome Sciences Centre; BC Cancer Agency","funders":"Canadian Institutes of Health Research; National Cancer Institute; BC Cancer Foundation; Michael Smith Health Research BC","keywords":"Rad50; Lymphoma; DNA repair; Biology; Genetics; Single-nucleotide polymorphism; Gene; Chromosomal translocation; Population; dbSNP; Cancer research; Medicine; Genotype; Immunology","authors":[{"name":"Johanna M. Schuetz","is_ca":true},{"name":"Amy C. MacArthur","is_ca":true},{"name":"Stephen Leach","is_ca":true},{"name":"Agnes S. Lai","is_ca":true},{"name":"Richard P. Gallagher","is_ca":true},{"name":"Joseph M. Connors","is_ca":true},{"name":"Randy D. Gascoyne","is_ca":true},{"name":"John J. Spinelli","is_ca":true},{"name":"Angela Brooks‐Wilson","is_ca":true}],"retraction":null,"screen_n_in":null,"score":{"opus":0.01685251547980425,"gpt":0.2848330792956911,"spread":0.2679805638158869,"validation_status":"score_only:v0-immature-baseline"},"prediction":{"model_version":"metacan-v3-hybrid-931329e0061c","candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0004578463,0.000283237,0.0002482898,0.0007797375,0.0002932808,0.000278788,0.0003221628,0.0004103203,0.004019633],"category_scores_gemma":[0.001695746,0.0001338972,0.0001887379,0.0007626935,0.0004181465,0.0001670233,0.0002383875,0.000289634,0.0002006243],"about_ca_system_candidate":false,"about_ca_system_consensus":false,"about_ca_system_score_codex":0.0001957471,"about_ca_system_score_gemma":0.0001262147,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_topic_score_codex":0.001339598,"about_ca_topic_score_gemma":0.001340238,"domain_scores_codex":[0.9997151,0.00008499947,0.00003310143,0.00008055551,0.00005315455,0.00003294749],"domain_scores_gemma":[0.9992353,0.0003681933,0.0002145087,0.0000456318,0.00003938764,0.00009694649],"domain_codex":null,"domain_gemma":null,"domain_candidate":null,"domain_consensus":null,"study_design_codex":"observational","study_design_gemma":"observational","study_design_scores_codex":[0.0006852031,0.00009626034,0.9868447,0.00003890453,0.0002226002,0.000735415,0.0001937576,0.0002021991,0.006630012,0.0001586624,0.0001741398,0.004018134],"study_design_scores_gemma":[0.00005155065,0.0001455173,0.9954671,0.00001018284,0.0001349377,0.002136575,0.0001099375,0.000354269,0.001025668,0.0002094214,0.000349836,0.00000503383],"study_design_candidate":"observational","study_design_consensus":"observational","genre_codex":"empirical","genre_gemma":"empirical","genre_scores_codex":[0.9994965,0.0001526782,0.00007819858,0.00002158509,0.000002146577,0.000004387688,0.00009329346,0.000003054651,0.0001481669],"genre_scores_gemma":[0.9995362,0.00007433058,0.0001305504,0.0000116652,0.000006674719,0.000004746691,0.0001307485,0.000001959736,0.0001032198],"genre_candidate":"empirical","genre_consensus":"empirical","teacher_disagreement_score":0.004019633,"threshold_uncertainty_score":0.01344705,"prediction_status":"machine_predicted_unvalidated"},"labels":[],"label_agreement":null},{"id":"W2142134526","doi":"10.1186/1471-2350-7-23","title":"Haplotype analysis suggest common founders in carriers of the recurrent BRCA2mutation, 3398delAAAAG, in French Canadian hereditary breast and/ovarian cancer families","year":2006,"lang":"en","type":"article","venue":"BMC Medical Genetics","topic":"BRCA gene mutations in cancer","field":"Biochemistry, Genetics and Molecular Biology","cited_by":33,"is_retracted":false,"has_abstract":true,"routes":{"ca_aff":true,"ca_fund":true,"ca_venue":false,"about_ca":true},"ca_institutions":"Hôtel-Dieu de Montréal; Université de Montréal; Hôpital Notre-Dame; McGill University Health Centre; Centre Hospitalier de l’Université de Montréal; McGill University","funders":"McGill University Health Centre; Canadian Institutes of Health Research; Cancer Research Society; McGill University","keywords":"Breast cancer; Ovarian cancer; Haplotype; Population; Genotyping; Biology; Genetics; Cancer; Mutation; Family history; Founder effect; Allele frequency; Oncology; Allele; Internal medicine; Medicine; Genotype; Gene","authors":[{"name":"Kathleen Klein Oros","is_ca":true},{"name":"Guy Leblanc","is_ca":true},{"name":"Suzanna L. Arcand","is_ca":true},{"name":"Zhen Zhou Shen","is_ca":true},{"name":"Chantal Perret","is_ca":true},{"name":"Anne‐Marie Mes‐Masson","is_ca":true},{"name":"William D. Foulkes","is_ca":true},{"name":"Parviz Ghadirian","is_ca":true},{"name":"Diane Provencher","is_ca":true},{"name":"Patricia N. Tonin","is_ca":true}],"retraction":null,"screen_n_in":null,"score":{"opus":0.008650065708799901,"gpt":0.2593901526536166,"spread":0.2507400869448167,"validation_status":"score_only:v0-immature-baseline"},"prediction":{"model_version":"metacan-v3-hybrid-931329e0061c","candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0002415633,0.0002599789,0.0002488315,0.001610423,0.001114694,0.0002833572,0.0003049884,0.0003572646,0.002284065],"category_scores_gemma":[0.001195119,0.0001626359,0.0002037527,0.000980111,0.0004981335,0.00007749826,0.0002226024,0.0001951936,0.0001215114],"about_ca_system_candidate":false,"about_ca_system_consensus":false,"about_ca_system_score_codex":0.001358205,"about_ca_system_score_gemma":0.001347616,"about_ca_topic_candidate":true,"about_ca_topic_consensus":false,"about_ca_topic_score_codex":0.4663662,"about_ca_topic_score_gemma":0.524064,"domain_scores_codex":[0.9996707,0.00003363872,0.00001601786,0.00008469009,0.00008605044,0.0001089143],"domain_scores_gemma":[0.9995207,0.000092323,0.0001477656,0.00003267133,0.0001068009,0.00009988277],"domain_codex":null,"domain_gemma":null,"domain_candidate":null,"domain_consensus":null,"study_design_codex":"observational","study_design_gemma":"observational","study_design_scores_codex":[0.000296058,0.00002715016,0.9769096,0.00001946417,0.00006551789,0.001987198,0.001199368,0.0001919146,0.01040145,0.0001182397,0.0003109035,0.008472987],"study_design_scores_gemma":[0.00001439675,0.00007010059,0.9940642,0.000007901788,0.00005735894,0.003480327,0.000429012,0.0002925768,0.0006544827,0.00004056194,0.0008796229,0.000009544456],"study_design_candidate":"observational","study_design_consensus":"observational","genre_codex":"empirical","genre_gemma":"empirical","genre_scores_codex":[0.9992549,0.0001408773,0.00008252099,0.00002380245,0.00000180714,0.000005731873,0.0001440893,0.000004773214,0.000341574],"genre_scores_gemma":[0.9994771,0.00007278675,0.00011299,0.00001500455,0.000002536542,0.000003579452,0.0001343797,0.000001956603,0.0001797911],"genre_candidate":"empirical","genre_consensus":"empirical","teacher_disagreement_score":0.5336338,"threshold_uncertainty_score":0.9273034,"prediction_status":"machine_predicted_unvalidated"},"labels":[],"label_agreement":null},{"id":"W1794475131","doi":"10.1186/1471-2350-6-16","title":"XLMR in MRX families 29, 32, 33 and 38 results from the dup24 mutation in the ARX (Aristaless related homeobox) gene","year":2005,"lang":"en","type":"article","venue":"BMC Medical Genetics","topic":"Genetics and Neurodevelopmental Disorders","field":"Biochemistry, Genetics and Molecular Biology","cited_by":33,"is_retracted":false,"has_abstract":true,"routes":{"ca_aff":true,"ca_fund":false,"ca_venue":false,"about_ca":false},"ca_institutions":"Queen's University; St. John’s Health Sciences Centre","funders":"National Health and Medical Research Council; Eunice Kennedy Shriver National Institute of Child Health and Human Development; Medical Research Council","keywords":"Genetics; Mutation; Biology; X chromosome; Gene duplication; Exon; Point mutation; Gene; Gene mutation; Molecular biology","authors":[{"name":"Monica L Stepp","is_ca":false},{"name":"A Lauren Cason","is_ca":false},{"name":"Merran Finnis","is_ca":false},{"name":"Marie Mangelsdorf","is_ca":false},{"name":"Elke Holinski‐Feder","is_ca":false},{"name":"David Macgregor","is_ca":false},{"name":"Andrée MacMillan","is_ca":true},{"name":"Jeanette JA Holden","is_ca":true},{"name":"Jozef Gécz","is_ca":false},{"name":"Roger E. Stevenson","is_ca":false},{"name":"Charles E. Schwartz","is_ca":false}],"retraction":null,"screen_n_in":null,"score":{"opus":0.01154604100003411,"gpt":0.2395520085461931,"spread":0.228005967546159,"validation_status":"score_only:v0-immature-baseline"},"prediction":{"model_version":"metacan-v3-hybrid-931329e0061c","candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.000313435,0.001205675,0.0003221971,0.001159441,0.0006786877,0.0001981559,0.0005460469,0.0006419919,0.007456372],"category_scores_gemma":[0.0008995711,0.0002641618,0.0003688401,0.0005144196,0.0005079882,0.0002120802,0.0005464439,0.0004285598,0.0007523119],"about_ca_system_candidate":false,"about_ca_system_consensus":false,"about_ca_system_score_codex":0.0002764097,"about_ca_system_score_gemma":0.0001777428,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_topic_score_codex":0.001099985,"about_ca_topic_score_gemma":0.00136406,"domain_scores_codex":[0.9996781,0.00005353646,0.00002707854,0.000110555,0.00007096143,0.00005985208],"domain_scores_gemma":[0.9997116,0.00008747348,0.0001176708,0.00001598057,0.00001233897,0.00005495689],"domain_codex":null,"domain_gemma":null,"domain_candidate":null,"domain_consensus":null,"study_design_codex":"observational","study_design_gemma":"observational","study_design_scores_codex":[0.00108051,0.0002976985,0.4579654,0.000312244,0.0001914965,0.3039968,0.00209802,0.0004506795,0.2023687,0.0008850259,0.00136374,0.02898967],"study_design_scores_gemma":[0.0001401918,0.00123267,0.5998168,0.0001258501,0.0002168012,0.3716202,0.0003937301,0.0004930051,0.02058146,0.0004258687,0.004912477,0.00004105742],"study_design_candidate":"observational","study_design_consensus":"observational","genre_codex":"empirical","genre_gemma":"empirical","genre_scores_codex":[0.9987625,0.0002199253,0.0002219954,0.00003886624,0.000003368766,0.00002180076,0.0001337974,0.00002904973,0.0005687117],"genre_scores_gemma":[0.9981019,0.0001783515,0.0007119984,0.00003330702,0.00001015903,0.00002241448,0.0003413639,0.00001074649,0.0005897661],"genre_candidate":"empirical","genre_consensus":"empirical","teacher_disagreement_score":0.007456372,"threshold_uncertainty_score":0.02494401,"prediction_status":"machine_predicted_unvalidated"},"labels":[],"label_agreement":null},{"id":"W2112927942","doi":"10.1186/1471-2350-10-3","title":"Genome screen in familial intracranial aneurysm","year":2009,"lang":"en","type":"article","venue":"BMC Medical Genetics","topic":"Intracranial Aneurysms: Treatment and Complications","field":"Medicine","cited_by":30,"is_retracted":false,"has_abstract":true,"routes":{"ca_aff":true,"ca_fund":false,"ca_venue":false,"about_ca":false},"ca_institutions":"Université de Montréal","funders":"National Institutes of Health; National Institute of Neurological Disorders and Stroke; National Human Genome Research Institute; Johns Hopkins University","keywords":"Genetic linkage; Linkage (software); Genetics; Chromosome; Human genetics; Biology; SNP; Disease; Gene; Medicine; Single-nucleotide polymorphism; Pathology; Genotype","authors":[{"name":"Tatiana Foroud","is_ca":false},{"name":"Laura Sauerbeck","is_ca":false},{"name":"Robert D. Brown","is_ca":false},{"name":"Craig S. Anderson","is_ca":false},{"name":"Daniel Woo","is_ca":false},{"name":"Dawn Kleindorfer","is_ca":false},{"name":"Matthew L. Flaherty","is_ca":false},{"name":"Ranjan Deka","is_ca":false},{"name":"Richard Hornung","is_ca":false},{"name":"Irene Meissner","is_ca":false},{"name":"Joan E. Bailey‐Wilson","is_ca":false},{"name":"Carl D. Langefeld","is_ca":true},{"name":"Guy A. Rouleau","is_ca":true},{"name":"E. Sander Connolly","is_ca":false},{"name":"Dongbing Lai","is_ca":false},{"name":"Daniel L. Koller","is_ca":false},{"name":"John Huston","is_ca":false},{"name":"Joseph P. Broderick","is_ca":false}],"retraction":null,"screen_n_in":null,"score":{"opus":0.02265834917284879,"gpt":0.2805405842406785,"spread":0.2578822350678297,"validation_status":"score_only:v0-immature-baseline"},"prediction":{"model_version":"metacan-v3-hybrid-931329e0061c","candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0003174398,0.0003476136,0.0003330583,0.0008118597,0.0004776806,0.0002545857,0.0003229764,0.0005096353,0.004038787],"category_scores_gemma":[0.001077809,0.0001026017,0.0003000211,0.0008122896,0.00009760504,0.00006577207,0.0002536795,0.0002525371,0.000696664],"about_ca_system_candidate":false,"about_ca_system_consensus":false,"about_ca_system_score_codex":0.000178162,"about_ca_system_score_gemma":0.0002950781,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_topic_score_codex":0.00354004,"about_ca_topic_score_gemma":0.005125538,"domain_scores_codex":[0.9998141,0.00005986227,0.00001196088,0.00004303276,0.00004640689,0.00002469945],"domain_scores_gemma":[0.9997435,0.0001099318,0.00004363342,0.00001830794,0.00004629094,0.0000383791],"domain_codex":null,"domain_gemma":null,"domain_candidate":null,"domain_consensus":null,"study_design_codex":"observational","study_design_gemma":"observational","study_design_scores_codex":[0.002162958,0.0004883998,0.7164606,0.0004613456,0.0006010698,0.02560574,0.0008856928,0.0009464049,0.06878842,0.001898219,0.03595469,0.1457464],"study_design_scores_gemma":[0.0002132401,0.0006824977,0.9301425,0.00008464439,0.0005788793,0.02381316,0.0002262667,0.002359782,0.0118055,0.001110675,0.02895456,0.00002837612],"study_design_candidate":"observational","study_design_consensus":"observational","genre_codex":"empirical","genre_gemma":"empirical","genre_scores_codex":[0.9782339,0.001883948,0.004151498,0.001220218,0.0001043247,0.0001561438,0.006528497,0.0004471457,0.007274307],"genre_scores_gemma":[0.9805978,0.0008032917,0.00796719,0.0006337222,0.00005233925,0.0001024491,0.006639214,0.00003564675,0.003168377],"genre_candidate":"empirical","genre_consensus":"empirical","teacher_disagreement_score":0.004038787,"threshold_uncertainty_score":0.01351106,"prediction_status":"machine_predicted_unvalidated"},"labels":[],"label_agreement":null},{"id":"W2121613431","doi":"10.1186/s12881-015-0183-0","title":"Novel VPS13B Mutations in Three Large Pakistani Cohen Syndrome Families Suggests a Baloch Variant with Autistic-Like Features","year":2015,"lang":"en","type":"article","venue":"BMC Medical Genetics","topic":"Blood disorders and treatments","field":"Biochemistry, Genetics and Molecular Biology","cited_by":29,"is_retracted":false,"has_abstract":true,"routes":{"ca_aff":true,"ca_fund":true,"ca_venue":false,"about_ca":false},"ca_institutions":"Mount Sinai Hospital; Douglas Mental Health University Institute; Université de Montréal; Queen's University; Hôpital Notre-Dame; Hôpital Rivière-des-Prairies; University of Toronto; University Health Network; Montreal Neurological Institute and Hospital; Hospital for Sick Children; Centre for Addiction and Mental Health","funders":"Canadian Institutes of Health Research; Medizinische Universität Graz; Hospital for Sick Children; Université de Montréal; University of Toronto; Centre for Addiction and Mental Health; Department of Psychiatry, University of Toronto; Queen's University; Karl-Franzens-Universität Graz; McGill University","keywords":"Genetics; Sanger sequencing; Biology; Haplotype; Exome sequencing; Human genetics; Consanguinity; Disease gene identification; Mutation; Founder effect; Intellectual disability; Phenotype; Autism; Runs of Homozygosity; Population; Exon; Gene; Allele; Genotype; Medicine; Psychiatry; Single-nucleotide polymorphism","authors":[{"name":"Muhammad Rafiq","is_ca":true},{"name":"Claire S. Leblond","is_ca":true},{"name":"Muhammad Arif Nadeem Saqib","is_ca":false},{"name":"Akshita K. Vincent","is_ca":true},{"name":"Amirthagowri Ambalavanan","is_ca":true},{"name":"Falak Sher Khan","is_ca":false},{"name":"Muhammad Ayaz","is_ca":false},{"name":"Naseema Shaheen","is_ca":false},{"name":"Dan Spiegelman","is_ca":true},{"name":"Ghazanfar Ali","is_ca":false},{"name":"Muhammad Aminuddin","is_ca":false},{"name":"Sandra B. Laurent","is_ca":true},{"name":"Huda Mahmood","is_ca":true},{"name":"Mehtab Christian","is_ca":true},{"name":"Nadir Ali","is_ca":false},{"name":"Alanna Fennell","is_ca":true},{"name":"Zohair Nanjiani","is_ca":false},{"name":"Gerald Egger","is_ca":true},{"name":"Chantal Caron","is_ca":true},{"name":"Ahmed Waqas","is_ca":false},{"name":"Muhammad Ayub","is_ca":true},{"name":"Saima Rasheed","is_ca":false},{"name":"Baudouin Forgeot d’Arc","is_ca":true},{"name":"Amelie Johnson","is_ca":true},{"name":"Joyce So","is_ca":true},{"name":"Muhammad Qasim Brohi","is_ca":false},{"name":"Laurent Mottron","is_ca":true},{"name":"Muhammad Ansar","is_ca":false},{"name":"John B. Vincent","is_ca":true},{"name":"Lan Xiong","is_ca":true}],"retraction":null,"screen_n_in":null,"score":{"opus":0.01488476577805392,"gpt":0.2643746207812714,"spread":0.2494898550032175,"validation_status":"score_only:v0-immature-baseline"},"prediction":{"model_version":"metacan-v3-hybrid-931329e0061c","candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0002331994,0.001730834,0.0004655366,0.001773847,0.001628878,0.000515317,0.0006388665,0.001312693,0.002653976],"category_scores_gemma":[0.001125774,0.0004860244,0.0004317056,0.0008977426,0.001369106,0.0002543797,0.001141432,0.0005481497,0.0002384203],"about_ca_system_candidate":false,"about_ca_system_consensus":false,"about_ca_system_score_codex":0.0007381017,"about_ca_system_score_gemma":0.0005792953,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_topic_score_codex":0.006267743,"about_ca_topic_score_gemma":0.007325552,"domain_scores_codex":[0.9995708,0.00004447173,0.00004492511,0.0001894939,0.00007446548,0.00007582774],"domain_scores_gemma":[0.9993101,0.0002432343,0.0001565643,0.00003468104,0.00006524151,0.0001901096],"domain_codex":null,"domain_gemma":null,"domain_candidate":null,"domain_consensus":null,"study_design_codex":"case_report","study_design_gemma":"observational","study_design_scores_codex":[0.0007442464,0.0002378941,0.2693807,0.0001729962,0.0001583823,0.6590813,0.004079544,0.0006470617,0.05004882,0.0006146588,0.0007489291,0.01408554],"study_design_scores_gemma":[0.0001269972,0.000352374,0.334975,0.00005907885,0.0001278746,0.6548621,0.001399065,0.0007087283,0.004903792,0.0004220334,0.001980421,0.00008252864],"study_design_candidate":"observational","study_design_consensus":null,"genre_codex":"empirical","genre_gemma":"empirical","genre_scores_codex":[0.9989263,0.00009236829,0.0001884612,0.00005003162,0.00000563512,0.0000184341,0.00009368295,0.00001070196,0.0006144673],"genre_scores_gemma":[0.9992135,0.00005743172,0.0003689283,0.00003795488,0.000007272277,0.00001233049,0.0000931363,0.000006084809,0.0002034569],"genre_candidate":"empirical","genre_consensus":"empirical","teacher_disagreement_score":0.006267743,"threshold_uncertainty_score":0.01246256,"prediction_status":"machine_predicted_unvalidated"},"labels":[],"label_agreement":null},{"id":"W2041568775","doi":"10.1186/1471-2350-14-5","title":"Contribution of the PALB2 c.2323C&gt;T [p.Q775X] Founder mutation in well-defined breast and/or ovarian cancer families and unselected ovarian cancer cases of French Canadian descent","year":2013,"lang":"en","type":"article","venue":"BMC Medical Genetics","topic":"BRCA gene mutations in cancer","field":"Biochemistry, Genetics and Molecular Biology","cited_by":29,"is_retracted":false,"has_abstract":true,"routes":{"ca_aff":true,"ca_fund":true,"ca_venue":false,"about_ca":true},"ca_institutions":"Université de Montréal; McGill University Health Centre; Jewish General Hospital; Centre Hospitalier de l’Université de Montréal; McGill University","funders":"Fonds de Recherche du Québec - Santé; Université de Montréal; Jewish General Hospital; Cancer Research Society; McGill University Health Centre; Canadian Breast Cancer Research Alliance; Ministero dello Sviluppo Economico; McGill University","keywords":"Ovarian cancer; PALB2; Breast cancer; Oncology; Population; Cancer; BRCA mutation; Internal medicine; Medicine; Serous fluid; Founder effect; Gynecology; Germline mutation; Mutation; Biology; Genetics; Genotype; Gene","authors":[{"name":"Marc Derek Tischkowitz","is_ca":true},{"name":"Nelly Sabbaghian","is_ca":true},{"name":"Nancy Hamel","is_ca":true},{"name":"Carly Pouchet","is_ca":true},{"name":"William D. Foulkes","is_ca":true},{"name":"Anne‐Marie Mes‐Masson","is_ca":true},{"name":"Diane Provencher","is_ca":true},{"name":"Patricia N. Tonin","is_ca":true}],"retraction":null,"screen_n_in":null,"score":{"opus":0.01230396050633896,"gpt":0.2596473779199003,"spread":0.2473434174135613,"validation_status":"score_only:v0-immature-baseline"},"prediction":{"model_version":"metacan-v3-hybrid-931329e0061c","candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.000488069,0.0008783069,0.00039387,0.003310969,0.002395589,0.0007843217,0.001136079,0.0009188583,0.003603149],"category_scores_gemma":[0.002594159,0.0004182132,0.0005577301,0.001802252,0.00106354,0.0001620438,0.0008127619,0.0004116746,0.0002396256],"about_ca_system_candidate":false,"about_ca_system_consensus":false,"about_ca_system_score_codex":0.003824747,"about_ca_system_score_gemma":0.00340227,"about_ca_topic_candidate":true,"about_ca_topic_consensus":true,"about_ca_topic_score_codex":0.6501606,"about_ca_topic_score_gemma":0.5662006,"domain_scores_codex":[0.9989378,0.00008922775,0.00007892907,0.0002583068,0.000279227,0.000356511],"domain_scores_gemma":[0.9988974,0.0002328247,0.0002614663,0.00006927028,0.0002334644,0.0003054387],"domain_codex":null,"domain_gemma":null,"domain_candidate":null,"domain_consensus":null,"study_design_codex":"observational","study_design_gemma":"observational","study_design_scores_codex":[0.0002558795,0.00002877736,0.9854082,0.00002090916,0.00008668465,0.008069572,0.0008982606,0.00009897441,0.002636348,0.00008859539,0.0002351814,0.002172593],"study_design_scores_gemma":[0.00001894349,0.00006876954,0.9838448,0.00002127835,0.00009709351,0.01335758,0.001071309,0.0002176882,0.0004212796,0.0000525775,0.000811812,0.00001688623],"study_design_candidate":"observational","study_design_consensus":"observational","genre_codex":"empirical","genre_gemma":"empirical","genre_scores_codex":[0.9987238,0.0002674467,0.00003546046,0.00003637089,0.000004653871,0.000009724101,0.0002517336,0.000003824576,0.0006669326],"genre_scores_gemma":[0.999343,0.0001272929,0.00006453946,0.00002266106,0.00000461805,0.000004974733,0.0002695389,0.000003538159,0.0001598446],"genre_candidate":"empirical","genre_consensus":"empirical","teacher_disagreement_score":0.3498394,"threshold_uncertainty_score":0.7037994,"prediction_status":"machine_predicted_unvalidated"},"labels":[],"label_agreement":null}]}