{"meta":{"query_hash":"ce827a0c6c09","filters":{"venue":"The Application of Clinical Genetics"},"cohort_total":18,"direct_labels_cover":0,"predictions_cover":18,"exported":18,"export_cap":100000,"truncated":false,"label_status":"direct model label, unvalidated","prediction_status":"machine_predicted_unvalidated (Codex and Gemma teacher distillation)","score_status":"score_only:v0-immature-baseline","snapshot":{"source":"OpenAlex, pinned release, all 482 partitions","release":"2026-06-24","frame_built":"2026-07-12"},"permalink":"https://metacan.xera.ac/q/ce827a0c6c09","api":"https://metacan.xera.ac/api/v1/cohort?venue=The+Application+of+Clinical+Genetics"},"results":[{"id":"W1728657678","doi":"10.2147/tacg.s55762","title":"Genetics of inherited primary arrhythmia disorders","year":2015,"lang":"en","type":"review","venue":"The Application of Clinical Genetics","topic":"Cardiac electrophysiology and arrhythmias","field":"Medicine","cited_by":25,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University Health Network","funders":"","keywords":"Catecholaminergic polymorphic ventricular tachycardia; Brugada syndrome; Medicine; Short QT syndrome; Genetic testing; Sudden cardiac death; Long QT syndrome; Sudden death; Heart disease; Disease; Genetic disorder; Abnormality; Cardiology; Internal medicine; QT interval; Ryanodine receptor 2; Psychiatry","score_opus":0.08643345458654295,"score_gpt":0.43729052285650255,"score_spread":0.3508570682699596,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1728657678","genre_codex":"review","genre_gemma":"review","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"review","genre_consensus":"review","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.001213654,0.9950055,0.00059246476,0.00016397721,0.00014273822,0.0016334394,0.00004522415,0.000023305503,0.00117973],"genre_scores_gemma":[0.0006516538,0.99613833,0.0014891394,0.00015124514,0.0009958075,0.0001086493,0.00024373912,0.000056661127,0.00016474334],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.9966792,0.00037525492,0.0020198703,0.00038302597,0.00033944403,0.00020322255],"domain_scores_gemma":[0.99598575,0.00075670664,0.001431617,0.0014007229,0.00029048888,0.00013474192],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0009878541,0.00029220027,0.0027317062,0.00006748295,0.000029262488,0.0000025266063,0.00032479953,0.00062518293,0.000010304251],"category_scores_gemma":[0.0001742026,0.00019425056,0.0009900031,0.0004014862,0.00067758525,0.000006881339,0.00016196455,0.0006593057,0.00004727915],"study_design_candidate":"design_other","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00008029896,0.00010118366,0.000037741473,0.0031160738,0.0003030635,0.0000010444182,0.0000131830375,0.000017012011,0.000016072625,0.00013855571,0.0005760979,0.9955997],"study_design_scores_gemma":[0.0004823066,0.00042541366,0.0008568875,0.0005714321,0.0019477833,0.000035491663,0.000003824524,0.00006168461,0.000010333683,0.00082272256,0.9946172,0.00016487531],"about_ca_topic_score_codex":0.0000028788897,"about_ca_topic_score_gemma":0.0000011765684,"teacher_disagreement_score":0.9954348,"about_ca_system_score_codex":0.0000268469,"about_ca_system_score_gemma":0.0007752723,"threshold_uncertainty_score":0.79213077},"labels":[],"label_agreement":null},{"id":"W1965416522","doi":"10.2147/tacg.s31276","title":"Skeletal muscle SIRT1 and the genetics of metabolic health: therapeutic activation by pharmaceuticals and exercise","year":2012,"lang":"en","type":"article","venue":"The Application of Clinical Genetics","topic":"Sirtuins and Resveratrol in Medicine","field":"Medicine","cited_by":24,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Queen's University","funders":"","keywords":"Mitochondrial biogenesis; Skeletal muscle; Mitochondrion; Medicine; Coactivator; Disease; Peroxisome proliferator-activated receptor; Bioinformatics; Sirtuin 1; Endocrinology; Internal medicine; Biology; Receptor; Gene; Cell biology; Genetics; Transcription factor; Downregulation and upregulation","score_opus":0.07932667963182922,"score_gpt":0.44487760047709474,"score_spread":0.3655509208452655,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1965416522","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.87950736,0.10410466,0.0052162297,0.00970881,0.00008543134,0.001219493,0.0000075045696,0.000010501677,0.00014000748],"genre_scores_gemma":[0.9414677,0.05525705,0.00074466487,0.002153023,0.00026774284,0.000036372217,0.000008689998,0.000014356682,0.00005040139],"study_design_codex":"design_other","study_design_gemma":"observational","domain_scores_codex":[0.9983655,0.00020884445,0.0008027828,0.00015342188,0.00029226168,0.00017717015],"domain_scores_gemma":[0.9980273,0.00085735647,0.00040638846,0.0004257714,0.00011058309,0.00017254816],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.002103557,0.00011449133,0.0005332356,0.000023851084,0.00006901898,0.0000044979574,0.00011913912,0.00009776923,0.00001315848],"category_scores_gemma":[0.0001249046,0.00005869123,0.000080744256,0.00013663016,0.0009634873,0.000017818707,0.00006008041,0.0002299796,0.0000019832123],"study_design_candidate":"design_other","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0002963444,0.00038079012,0.013698746,0.00012020516,0.00013297604,2.4424502e-8,0.0005476,0.0000059799822,0.013325969,0.0032963287,0.000384109,0.9678109],"study_design_scores_gemma":[0.011787976,0.00069492,0.6887015,0.00011144036,0.0015097884,0.000014553405,0.0006602257,0.012055533,0.03220581,0.0019235723,0.25010285,0.00023186089],"about_ca_topic_score_codex":0.000014617958,"about_ca_topic_score_gemma":3.3093897e-7,"teacher_disagreement_score":0.96757907,"about_ca_system_score_codex":0.0000031502477,"about_ca_system_score_gemma":0.00004403018,"threshold_uncertainty_score":0.3550009},"labels":[],"label_agreement":null},{"id":"W1969833817","doi":"10.2147/tacg.s37325","title":"The genetic basis of ankylosing spondylitis: new insights into disease pathogenesis","year":2014,"lang":"en","type":"review","venue":"The Application of Clinical Genetics","topic":"Spondyloarthritis Studies and Treatments","field":"Medicine","cited_by":105,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Toronto Rehabilitation Institute; University Health Network","funders":"Institute of Musculoskeletal Health and Arthritis; Canadian Institutes of Health Research; Arthritis Society","keywords":"Ankylosing spondylitis; Genome-wide association study; Disease; Genetic association; Medicine; Human leukocyte antigen; HLA-B27; Genetic predisposition; Spondylitis; Genetics; Immunology; Biology; Single-nucleotide polymorphism; Gene; Pathology; Genotype; Antigen","score_opus":0.0752570273174986,"score_gpt":0.41762999530894507,"score_spread":0.34237296799144645,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1969833817","genre_codex":"review","genre_gemma":"review","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"review","genre_consensus":"review","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.0016352668,0.9950195,0.0010030604,0.00025021387,0.00016229085,0.0017079787,0.000064369,0.00001688353,0.00014046961],"genre_scores_gemma":[0.0025888935,0.9942227,0.0018223053,0.00009807361,0.0006977961,0.00019733098,0.000120734665,0.000058407728,0.0001937417],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.9963072,0.00037064217,0.0022106445,0.0004519808,0.0004432695,0.00021627142],"domain_scores_gemma":[0.9945679,0.0018039094,0.0013970066,0.0017223617,0.00022961551,0.00027924925],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00053017924,0.00033811724,0.0019164244,0.00005250251,0.0001753289,0.000012670586,0.00048402292,0.00022851177,0.000017104514],"category_scores_gemma":[0.0004837583,0.00017927185,0.00096058426,0.00033414704,0.00050335814,0.000007829864,0.00020597647,0.00022395293,0.000040659255],"study_design_candidate":"design_other","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.000089156754,0.00015641355,0.00059467443,0.0019783326,0.00037048446,0.0000023054924,0.000029258665,0.0000014771066,0.0000011131939,0.0004453097,0.00021449296,0.996117],"study_design_scores_gemma":[0.00068997836,0.00026492533,0.0077544767,0.0018870924,0.0039403895,0.0000049107825,0.000012413751,0.000042438674,0.000006554911,0.0013111142,0.98393726,0.00014844933],"about_ca_topic_score_codex":0.000036903904,"about_ca_topic_score_gemma":0.000021342526,"teacher_disagreement_score":0.9959685,"about_ca_system_score_codex":0.000029349898,"about_ca_system_score_gemma":0.0004726291,"threshold_uncertainty_score":0.7310494},"labels":[],"label_agreement":null},{"id":"W2034221138","doi":"10.2147/tacg.s8380","title":"Allergic rhinitis and genetic components: focus on Toll-like receptors (TLRs) gene polymorphism","year":2010,"lang":"en","type":"article","venue":"The Application of Clinical Genetics","topic":"Pediatric health and respiratory diseases","field":"Health Professions","cited_by":12,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Saskatchewan; University of Alberta","funders":"Canadian Institutes of Health Research","keywords":"Immunology; Immune system; Toll-like receptor; Innate immune system; Medicine; Allergy; Biology","score_opus":0.0866217281603684,"score_gpt":0.44150352142701776,"score_spread":0.35488179326664937,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2034221138","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9918195,0.0010721531,0.000700074,0.0031132926,0.00101822,0.0011524915,0.000047664937,0.00005492989,0.001021666],"genre_scores_gemma":[0.9873701,0.0038778933,0.0015767709,0.0051641506,0.0015342259,0.00020625402,0.000021886737,0.000033669654,0.00021505855],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9967664,0.0006116069,0.0015094233,0.0003808386,0.0003440772,0.00038764725],"domain_scores_gemma":[0.99572873,0.0020476182,0.0006966189,0.00086283684,0.00016231588,0.0005019031],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0009788703,0.00017837163,0.00041338173,0.00006000263,0.00044758376,0.0000057615034,0.00042447879,0.0003766283,0.0001484842],"category_scores_gemma":[0.00037380017,0.00012616774,0.0001084926,0.00016139563,0.00035144854,0.000017285498,0.00014785721,0.00085446733,0.00029976552],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0008201809,0.001179763,0.50452745,0.0003782793,0.00012103269,0.000006072708,0.0003789515,0.000046641908,0.0066169095,0.0033214618,0.023938082,0.4586652],"study_design_scores_gemma":[0.0017072761,0.00028646784,0.6679048,0.000020224283,0.00007874659,0.0000026446799,0.00006708092,0.0005312873,0.00014967614,0.0028895056,0.32615456,0.0002077077],"about_ca_topic_score_codex":0.00007881732,"about_ca_topic_score_gemma":0.000039124083,"teacher_disagreement_score":0.45845747,"about_ca_system_score_codex":0.000012140615,"about_ca_system_score_gemma":0.0003352355,"threshold_uncertainty_score":0.51449716},"labels":[],"label_agreement":null},{"id":"W2064411615","doi":"10.2147/tacg.s10604","title":"Alpha1-antitrypsin deficiency: a clinical-genetic overview","year":2011,"lang":"en","type":"article","venue":"The Application of Clinical Genetics","topic":"Chronic Obstructive Pulmonary Disease (COPD) Research","field":"Medicine","cited_by":43,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"St. Paul's Hospital; Children's & Women's Health Centre of British Columbia; University of British Columbia","funders":"","keywords":"Alpha 1-antitrypsin deficiency; Medicine; Allele; Liver disease; Disease; Genetic disorder; Hepatitis; Genotype; Gastroenterology; Internal medicine; Immunology; Pathology; Gene; Biology; Genetics","score_opus":0.18873807786198735,"score_gpt":0.4550121470766242,"score_spread":0.2662740692146368,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2064411615","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9557935,0.017149413,0.006743888,0.0010155754,0.00026922862,0.002026473,0.000033614593,0.00007491955,0.016893402],"genre_scores_gemma":[0.9818991,0.0061124936,0.010407388,0.0007110103,0.0003487596,0.000079350146,0.00001468124,0.000041541054,0.00038571074],"study_design_codex":"design_other","study_design_gemma":"observational","domain_scores_codex":[0.996161,0.0003861526,0.0019092128,0.0005693796,0.0006253601,0.00034891712],"domain_scores_gemma":[0.9962148,0.0006503687,0.0005559402,0.001795096,0.00042633753,0.00035747187],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0019244659,0.00019447738,0.0006767913,0.000057949594,0.00007927306,0.00000816064,0.00067519455,0.00021993571,0.00047188712],"category_scores_gemma":[0.0005866255,0.00013967876,0.0004851166,0.00044846995,0.0011267767,0.000025609506,0.00027404143,0.00047025247,0.00045975723],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00047957522,0.0020168773,0.47805512,0.0003319663,0.0001458688,0.0000084133635,0.00009526157,0.000007808664,0.0002184606,0.0049354197,0.0017519945,0.51195323],"study_design_scores_gemma":[0.0012388948,0.0003590556,0.9659204,0.00003951587,0.00030747754,0.000014494241,0.00005071222,0.002160231,0.00033229706,0.006371877,0.023064137,0.00014093671],"about_ca_topic_score_codex":0.000051402378,"about_ca_topic_score_gemma":0.00000758317,"teacher_disagreement_score":0.51181227,"about_ca_system_score_codex":0.000027878265,"about_ca_system_score_gemma":0.0004969339,"threshold_uncertainty_score":0.59094024},"labels":[],"label_agreement":null},{"id":"W2077740415","doi":"10.2147/tacg.s21953","title":"Clinical applications of schizophrenia genetics: genetic diagnosis, risk, and counseling in the molecular era","year":2012,"lang":"en","type":"article","venue":"The Application of Clinical Genetics","topic":"Congenital heart defects research","field":"Biochemistry, Genetics and Molecular Biology","cited_by":72,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Toronto; Centre for Addiction and Mental Health","funders":"Canadian Institutes of Health Research; U.S. Public Health Service","keywords":"Schizophrenia (object-oriented programming); Penetrance; Disease; Medicine; Psychiatric genetics; Personalized medicine; Human genetics; Genetic counseling; Molecular genetics; Psychiatry; Bioinformatics; Genetics; Biology; Pathology","score_opus":0.03160096068000695,"score_gpt":0.4015661789743646,"score_spread":0.36996521829435763,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2077740415","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.95943373,0.020925388,0.018082865,0.00016591795,0.00004547957,0.0011813679,0.00003055082,0.0000049914615,0.00012967916],"genre_scores_gemma":[0.973828,0.019187415,0.005909274,0.0002112065,0.00040480494,0.00040059155,0.000022696564,0.000025678864,0.000010300304],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.996841,0.00085872243,0.0012801426,0.00037014153,0.0003549754,0.00029501],"domain_scores_gemma":[0.9969607,0.0010405564,0.00041760385,0.0012330532,0.0002127121,0.00013539204],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0035323126,0.00016169586,0.00033567438,0.000045919995,0.000080774,0.000014356382,0.0006753315,0.0002530245,0.000006121665],"category_scores_gemma":[0.00046834289,0.000115746814,0.00018848926,0.0002866132,0.00068161834,0.0000034431694,0.0002448692,0.0004246671,0.000013528114],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.000113841816,0.0004946091,0.5711496,0.00004389604,0.000066837965,2.0425503e-7,0.00009738777,0.00013434337,0.0062752147,0.00042291387,0.00010081121,0.42110032],"study_design_scores_gemma":[0.0013761194,0.0005806303,0.9049697,0.00001678704,0.00018982874,0.000012341542,0.00016113532,0.0017214393,0.0148559045,0.0016709437,0.074164934,0.0002802728],"about_ca_topic_score_codex":0.000030831994,"about_ca_topic_score_gemma":0.000048212645,"teacher_disagreement_score":0.42082006,"about_ca_system_score_codex":0.0000041341877,"about_ca_system_score_gemma":0.000105039006,"threshold_uncertainty_score":0.47200182},"labels":[],"label_agreement":null},{"id":"W2088888970","doi":"10.2147/tacg.s35602","title":"Identification of trisomy 18, trisomy 13, and Down syndrome from maternal plasma","year":2014,"lang":"en","type":"review","venue":"The Application of Clinical Genetics","topic":"Prenatal Screening and Diagnostics","field":"Medicine","cited_by":20,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Centre Hospitalier Universitaire Sainte-Justine; University of British Columbia; Université Laval; Université de Montréal; Centre hospitalier universitaire de Québec","funders":"Genome Alberta; Centre Hospitalier Universitaire de Québec; Genome Canada; Ministère de la Santé et des Services sociaux; Ministère de la Santé; Genome British Columbia","keywords":"Trisomy; Amniocentesis; Chorionic villus sampling; Prenatal diagnosis; Down syndrome; Miscarriage; Medicine; Obstetrics; Obstetrics and gynaecology; Gynecology; Family medicine; Pregnancy; Fetus; Genetics; Biology; Psychiatry","score_opus":0.08841173031584204,"score_gpt":0.42538592724070196,"score_spread":0.3369741969248599,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2088888970","genre_codex":"review","genre_gemma":"review","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"review","genre_consensus":"review","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.02311706,0.9632257,0.01108218,0.00012813899,0.00016905289,0.0016641571,0.00032489386,0.0000307886,0.00025803113],"genre_scores_gemma":[0.07522296,0.9227489,0.0012103532,0.000035114193,0.00026293626,0.00009093754,0.00026097344,0.000035187277,0.00013263634],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.99619216,0.00025678953,0.0026377616,0.0003996512,0.0003746831,0.00013897594],"domain_scores_gemma":[0.99344885,0.0030762453,0.0020906115,0.001078236,0.00015639793,0.00014967579],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0011735575,0.00024212271,0.001934695,0.00007010948,0.00003443731,0.000014551337,0.0004394774,0.00045733224,0.00002207129],"category_scores_gemma":[0.00087185454,0.00016219195,0.00038295976,0.00017782643,0.00033550704,0.00001409461,0.00015339449,0.00039896576,0.000071074035],"study_design_candidate":"design_other","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.000060212285,0.00013713405,0.0018061604,0.0026146164,0.00020732067,9.921778e-7,0.000008931467,0.0000034673737,0.000013066075,0.0001503523,0.0003239115,0.99467385],"study_design_scores_gemma":[0.002018301,0.0005143921,0.033919565,0.0042830636,0.005296032,0.00007694766,0.000009101403,0.001457589,0.00038066885,0.0011938692,0.9505165,0.00033397414],"about_ca_topic_score_codex":0.00006214923,"about_ca_topic_score_gemma":0.0000023524358,"teacher_disagreement_score":0.9943399,"about_ca_system_score_codex":0.000011225472,"about_ca_system_score_gemma":0.00012335129,"threshold_uncertainty_score":0.66139954},"labels":[],"label_agreement":null},{"id":"W2255520670","doi":"10.2147/tacg.s85361","title":"Non-invasive prenatal testing for fetal chromosome abnormalities: review of clinical and ethical issues","year":2016,"lang":"en","type":"review","venue":"The Application of Clinical Genetics","topic":"Prenatal Screening and Diagnostics","field":"Medicine","cited_by":50,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Centre Hospitalier Universitaire Sainte-Justine; University of British Columbia; Université Laval; Université de Montréal; Centre hospitalier universitaire de Québec","funders":"Genome Alberta; Canadian Institutes of Health Research; Genome British Columbia; Genome Canada","keywords":"Medicine; Cell-free fetal DNA; Prenatal diagnosis; Autonomy; Neglect; Ethical issues; Prenatal screening; Pregnancy; Obstetrics; Fetus; Psychiatry; Genetics; Biology; Engineering ethics","score_opus":0.18353555170784,"score_gpt":0.5007858632339736,"score_spread":0.3172503115261336,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2255520670","genre_codex":"review","genre_gemma":"review","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"review","genre_consensus":"review","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.000095865034,0.9930093,0.0019208379,0.0008397452,0.00014008311,0.0030859015,0.00041367233,0.000028555734,0.00046602043],"genre_scores_gemma":[0.00034047107,0.98561585,0.011398382,0.0006200146,0.0013603063,0.00030064562,0.00019338808,0.000053262593,0.0001177066],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.9938129,0.00039158188,0.0045222687,0.00056205894,0.00045479333,0.00025636086],"domain_scores_gemma":[0.96833706,0.026899312,0.0025720843,0.0011881025,0.0007243641,0.00027910314],"candidate_categories":["metaresearch"],"consensus_categories":[],"category_scores_codex":[0.0049859937,0.00035225635,0.003768096,0.000042321237,0.00005527468,0.000007838924,0.0005176821,0.0010349146,0.000013568736],"category_scores_gemma":[0.025890684,0.00020130303,0.0009641376,0.00020056007,0.0012163147,0.000016209788,0.00033005717,0.00097114505,0.000021037069],"study_design_candidate":"design_other","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00005034911,0.00010718877,0.00061921985,0.10187692,0.00022127057,0.0000010895849,0.000008584895,1.0724927e-7,5.8018855e-7,0.0005169772,0.0010433048,0.8955544],"study_design_scores_gemma":[0.001281292,0.0015005638,0.0007748505,0.19826497,0.0032885456,0.000056570458,0.000007538501,0.000096657044,0.000037021047,0.0006471696,0.793738,0.00030683033],"about_ca_topic_score_codex":0.000011242535,"about_ca_topic_score_gemma":0.0000011797242,"teacher_disagreement_score":0.8952476,"about_ca_system_score_codex":0.00000967475,"about_ca_system_score_gemma":0.0007937549,"threshold_uncertainty_score":0.98231465},"labels":[],"label_agreement":null},{"id":"W2472373950","doi":"10.2147/tacg.s86420","title":"Alagille syndrome: clinical perspectives","year":2016,"lang":"en","type":"review","venue":"The Application of Clinical Genetics","topic":"Pediatric Hepatobiliary Diseases and Treatments","field":"Medicine","cited_by":145,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Hospital for Sick Children; University of Toronto; Mount Sinai Hospital","funders":"","keywords":"Alagille syndrome; Medicine; Bioinformatics; Computational biology; Internal medicine; Biology; Cholestasis","score_opus":0.13671805828934358,"score_gpt":0.5137875112094893,"score_spread":0.3770694529201457,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2472373950","genre_codex":"review","genre_gemma":"review","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"review","genre_consensus":"review","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.00085517106,0.9953207,0.0002834483,0.00023230765,0.00016670398,0.0018453314,0.00014364587,0.000039247207,0.0011134719],"genre_scores_gemma":[0.0021148736,0.9954108,0.00048769178,0.00008384305,0.00083583326,0.00019749775,0.00007560188,0.000054375527,0.0007394678],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.9958022,0.00043927794,0.0025651602,0.00061637716,0.0003590113,0.00021796375],"domain_scores_gemma":[0.994313,0.002262968,0.0012712759,0.0016245286,0.00020557785,0.00032266424],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0011509871,0.0003116749,0.0024824175,0.000055967987,0.00005109934,0.000006318202,0.0004399981,0.0005108286,0.00010155796],"category_scores_gemma":[0.0006234589,0.00015621197,0.0017965737,0.00024157696,0.00049727026,0.000013010319,0.00016425643,0.00041655832,0.0006719912],"study_design_candidate":"design_other","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00002882275,0.0008660383,0.0031229712,0.0011360582,0.00058671884,0.00000705203,0.0000045787338,3.4145074e-8,1.1154004e-8,0.00031270582,0.0008421899,0.99309283],"study_design_scores_gemma":[0.00083664886,0.00042785445,0.0057278657,0.0010011783,0.004072058,0.00004740997,0.0000115708535,0.00000892655,7.326322e-8,0.00034567068,0.9873639,0.00015687822],"about_ca_topic_score_codex":0.0000040391988,"about_ca_topic_score_gemma":4.082124e-7,"teacher_disagreement_score":0.99293596,"about_ca_system_score_codex":0.00003893503,"about_ca_system_score_gemma":0.00072549115,"threshold_uncertainty_score":0.86373115},"labels":[],"label_agreement":null},{"id":"W2755101109","doi":"10.2147/tacg.s127129","title":"Primary ciliary dyskinesia: mechanisms and management","year":2017,"lang":"en","type":"review","venue":"The Application of Clinical Genetics","topic":"Cystic Fibrosis Research Advances","field":"Medicine","cited_by":72,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Mount Sinai Hospital; Institute for Clinical Evaluative Sciences; University Health Network; University of Toronto; SickKids Foundation; Hospital for Sick Children","funders":"National Heart, Lung, and Blood Institute","keywords":"Primary ciliary dyskinesia; Dyskinesia; Medicine; Primary (astronomy); Pathology; Internal medicine; Bronchiectasis; Parkinson's disease; Disease","score_opus":0.18266994775855644,"score_gpt":0.5129291240150126,"score_spread":0.3302591762564561,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2755101109","genre_codex":"review","genre_gemma":"review","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"review","genre_consensus":"review","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.000004954309,0.98589486,0.008210998,0.0002553381,0.00007276379,0.002616368,0.000024628689,0.000019604917,0.0029005143],"genre_scores_gemma":[0.000013599147,0.9674938,0.030893452,0.000086031614,0.00020843331,0.00029725622,0.00008207439,0.000035268517,0.00089011464],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.99756354,0.00014574209,0.0012208173,0.0004214885,0.0004699557,0.0001784463],"domain_scores_gemma":[0.9963293,0.0008237961,0.0008754233,0.0017126736,0.00011212749,0.00014669893],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0013790827,0.00021796148,0.001595004,0.00006076118,0.000077989855,0.00001785123,0.00057536986,0.00022414338,0.000010234547],"category_scores_gemma":[0.00026175563,0.0001328219,0.0003135622,0.000098551274,0.00046364332,0.000014276428,0.0004588667,0.00037638625,0.00005618536],"study_design_candidate":"not_applicable","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.000030203351,0.00008251451,0.0000077992745,0.014997586,0.00016740226,0.0000026263851,0.0000016639513,1.6852326e-7,0.0000027517326,0.0018490975,0.00034024354,0.98251796],"study_design_scores_gemma":[0.0003554231,0.00016444255,0.001282469,0.0021767255,0.0011428535,0.000020832678,0.0000025108707,0.000036773046,0.0000025693912,0.0023289262,0.992379,0.000107475615],"about_ca_topic_score_codex":0.000001850112,"about_ca_topic_score_gemma":8.6061175e-7,"teacher_disagreement_score":0.9920387,"about_ca_system_score_codex":0.00002244985,"about_ca_system_score_gemma":0.00016136956,"threshold_uncertainty_score":0.54163194},"labels":[],"label_agreement":null},{"id":"W2799416953","doi":"10.2147/tacg.s150982","title":"Fetal chondrodysplasia punctata associated with maternal autoimmune diseases: a review","year":2018,"lang":"en","type":"review","venue":"The Application of Clinical Genetics","topic":"Peroxisome Proliferator-Activated Receptors","field":"Biochemistry, Genetics and Molecular Biology","cited_by":13,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"SickKids Foundation; Hospital for Sick Children; University of Toronto","funders":"","keywords":"Chondrodysplasia punctata; Medicine; Fetus; Abnormality; Peroxisomal disorder; Etiology; Malabsorption; Pregnancy; Disease; Rickets; Endocrinology; Pathology; Internal medicine; Vitamin D and neurology; Genetics; Peroxisome; Biology","score_opus":0.04413300815245317,"score_gpt":0.387956926680517,"score_spread":0.3438239185280638,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2799416953","genre_codex":"review","genre_gemma":"review","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"review","genre_consensus":"review","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.0009323026,0.9962054,0.00052778726,0.000058308175,0.0001733817,0.0016699291,0.00026838863,0.000026950993,0.00013757766],"genre_scores_gemma":[0.00054954283,0.9960625,0.0002999066,0.0002295905,0.0005036173,0.0003948282,0.0014815091,0.00010041858,0.00037806787],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.9962327,0.00060546235,0.0017677518,0.0007133771,0.00038329163,0.00029741798],"domain_scores_gemma":[0.9956807,0.00017943658,0.0019956646,0.0016694416,0.00031754837,0.00015720473],"candidate_categories":["metaepi_narrow"],"consensus_categories":[],"category_scores_codex":[0.0009008222,0.00047995205,0.0017189119,0.00003500863,0.00008360255,0.000022446342,0.0012508639,0.00056671846,0.000037417998],"category_scores_gemma":[0.00058056077,0.00028604452,0.00063657644,0.00032283086,0.0005867003,0.0000031052,0.00034930324,0.00040933117,0.000087414286],"study_design_candidate":"not_applicable","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00011984364,0.0005299701,0.00063801603,0.0099157,0.001990829,0.0000012992932,0.0000049612477,0.0000025409124,0.00018702372,0.00002116722,0.008178177,0.9784105],"study_design_scores_gemma":[0.00034664964,0.00039236134,0.00030382295,0.0060188747,0.0016668332,0.000016282322,0.0000010369062,0.000014332793,0.00029692505,0.000015321208,0.99057984,0.00034769927],"about_ca_topic_score_codex":0.0000023838888,"about_ca_topic_score_gemma":0.0000032897021,"teacher_disagreement_score":0.98240167,"about_ca_system_score_codex":0.000023463203,"about_ca_system_score_gemma":0.00056049414,"threshold_uncertainty_score":0.9999592},"labels":[],"label_agreement":null},{"id":"W2954241695","doi":"10.2147/tacg.s187481","title":"&lt;p&gt;Current understanding and treatment of cardiac and skeletal muscle pathology in laminin-α2 chain-deficient congenital muscular dystrophy&lt;/p&gt;","year":2019,"lang":"en","type":"article","venue":"The Application of Clinical Genetics","topic":"Muscle Physiology and Disorders","field":"Biochemistry, Genetics and Molecular Biology","cited_by":66,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Muscular Dystrophy Canada; University of Alberta","funders":"Canadian Institutes of Health Research; Alberta Innovates; Muscular Dystrophy Canada; Children's Health Research Institute; Women and Children's Health Research Institute; Ministry of Advanced Education, Government of Alberta; Alberta Innovates - Health Solutions","keywords":"Congenital muscular dystrophy; Laminin; Medicine; Muscular dystrophy; Skeletal muscle; Cardiac muscle; Dystroglycan; ITGA7; Pathology; Extracellular matrix; Internal medicine; Endocrinology; Biology; Genetics","score_opus":0.029998518805905504,"score_gpt":0.31351164828135586,"score_spread":0.2835131294754504,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2954241695","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99246466,0.005804599,0.0008039046,0.00007923779,0.00010669255,0.00049017597,0.00003195207,0.0000034925874,0.00021528195],"genre_scores_gemma":[0.99305904,0.0065803425,0.00015779382,0.000026438829,0.00006266049,0.000035593224,0.000050033395,0.000011615224,0.000016512802],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.99874043,0.00016669209,0.00048347923,0.0003560567,0.00009332064,0.00016000867],"domain_scores_gemma":[0.9991285,0.00012729042,0.00021891872,0.0004255413,0.000045583554,0.000054123004],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0003340848,0.00013721477,0.00034605476,0.00003034419,0.000033097735,0.000003699717,0.000117039366,0.00016582602,0.000003504536],"category_scores_gemma":[0.000036086283,0.000107851796,0.00011437808,0.00006623468,0.00042968275,0.0000018309825,0.00009934992,0.00006397685,0.000002391043],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00031997586,0.0007158158,0.039081525,0.00007798932,0.00016464035,5.267295e-7,0.0003192854,0.00026476014,0.80781907,0.0076577086,0.0000278968,0.14355083],"study_design_scores_gemma":[0.004596748,0.0045083542,0.9309661,0.0000224592,0.00021649695,0.0000046858627,0.0005305833,0.0021344074,0.0150179425,0.002560792,0.038959444,0.0004819821],"about_ca_topic_score_codex":0.00000334838,"about_ca_topic_score_gemma":0.000016414262,"teacher_disagreement_score":0.89188457,"about_ca_system_score_codex":0.000009610618,"about_ca_system_score_gemma":0.00004203295,"threshold_uncertainty_score":0.43980685},"labels":[],"label_agreement":null},{"id":"W3013038946","doi":"10.2147/tacg.s210325","title":"&lt;p&gt;Alternating Hemiplegia of Childhood: Understanding the Genotype–Phenotype Relationship of ATP1A3 Variations&lt;/p&gt;","year":2020,"lang":"en","type":"review","venue":"The Application of Clinical Genetics","topic":"Ion Transport and Channel Regulation","field":"Biochemistry, Genetics and Molecular Biology","cited_by":40,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Centre for Movement Disorders","funders":"","keywords":"Parkinsonism; Dystonia; Medicine; Disease; Phenotype; Epilepsy; Bioinformatics; Neuroscience; Pediatrics; Genetics; Internal medicine; Psychology; Biology; Gene; Psychiatry","score_opus":0.09345539065902139,"score_gpt":0.36551954947782445,"score_spread":0.2720641588188031,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W3013038946","genre_codex":"review","genre_gemma":"review","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"review","genre_consensus":"review","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.0038979463,0.84241426,0.15029962,0.00025915404,0.00031052166,0.0016863979,0.00016096613,0.000019343406,0.00095178623],"genre_scores_gemma":[0.38024488,0.6170652,0.0013234584,0.00003061717,0.0006114554,0.000047466012,0.000553312,0.000051807936,0.00007181496],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.9967111,0.00029854718,0.0020514792,0.0004041019,0.0003721506,0.00016262972],"domain_scores_gemma":[0.9958389,0.00057913124,0.002328985,0.000948817,0.00023873843,0.00006547763],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0011642448,0.0002676762,0.00088947255,0.000048792608,0.00011530264,0.000009491085,0.0007567445,0.00046987645,0.0000104157325],"category_scores_gemma":[0.00035051408,0.00018447617,0.00057916675,0.0003767569,0.00030817042,0.0000033989172,0.0001272367,0.00027852764,0.000007661666],"study_design_candidate":"not_applicable","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00021778564,0.0005288382,0.0011630891,0.004699604,0.0014912931,4.536301e-7,0.000583396,0.00220574,0.0069465516,0.11718283,0.00040787307,0.8645725],"study_design_scores_gemma":[0.0010630162,0.00067921565,0.008111565,0.001053002,0.002710852,0.000007827846,0.00007153897,0.0019810551,0.0016105132,0.0112245595,0.9707941,0.0006927429],"about_ca_topic_score_codex":0.0000023826303,"about_ca_topic_score_gemma":0.000008173018,"teacher_disagreement_score":0.97038627,"about_ca_system_score_codex":0.000020067091,"about_ca_system_score_gemma":0.00032203147,"threshold_uncertainty_score":0.752272},"labels":[],"label_agreement":null},{"id":"W3133905552","doi":"10.2147/tacg.s260755","title":"Identifying Potential Mutations Responsible for Cases of Pulmonary Arterial Hypertension","year":2021,"lang":"en","type":"review","venue":"The Application of Clinical Genetics","topic":"Pulmonary Hypertension Research and Treatments","field":"Medicine","cited_by":4,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Institut du Savoir Montfort; Montfort Hospital","funders":"","keywords":"BMPR2; Penetrance; Bioinformatics; Pulmonary hypertension; Epigenetics; Disease; Gene; Bone morphogenetic protein; Germline mutation; Medicine; Bone morphogenetic protein receptor; ACVRL1; Mutation; Genetics; Biology; Internal medicine; Phenotype; Endoglin","score_opus":0.28898698921965477,"score_gpt":0.5066746634414755,"score_spread":0.21768767422182073,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W3133905552","genre_codex":"review","genre_gemma":"review","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"review","genre_consensus":"review","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.0024807188,0.9925643,0.0017084213,0.00018447984,0.00021437787,0.0025027608,0.00028048593,0.000015491845,0.000048949612],"genre_scores_gemma":[0.008011208,0.9848752,0.0048451577,0.000048927723,0.0003637946,0.00030842854,0.0012019135,0.000045293098,0.00030006896],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.9969362,0.00033166324,0.0017002533,0.0004116949,0.0004226923,0.00019751556],"domain_scores_gemma":[0.99509287,0.0022888207,0.0008264876,0.0009496207,0.0006904401,0.00015177071],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0007490549,0.00021729204,0.0018400693,0.000118294694,0.000094308256,0.000009670017,0.0002459448,0.00030588612,0.000024850568],"category_scores_gemma":[0.0009487925,0.00014140306,0.0009993588,0.00031418513,0.00027572067,0.000017844188,0.00014152519,0.00024342765,0.000017699891],"study_design_candidate":"design_other","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0003607436,0.0010914316,0.000024400422,0.0033387584,0.00046785717,0.00013395463,0.0000029962005,0.0000028620557,0.0006761632,0.00011156213,0.00033084137,0.99345845],"study_design_scores_gemma":[0.0018902258,0.00080351625,0.0010563115,0.0045917965,0.007606289,0.0016634053,0.00006478578,0.0013635064,0.00046612343,0.0008250361,0.9793877,0.0002813021],"about_ca_topic_score_codex":0.000010976193,"about_ca_topic_score_gemma":8.618519e-7,"teacher_disagreement_score":0.9931771,"about_ca_system_score_codex":0.000016027745,"about_ca_system_score_gemma":0.0008981504,"threshold_uncertainty_score":0.57662493},"labels":[],"label_agreement":null},{"id":"W4287379005","doi":"10.2147/tacg.s364543","title":"Utility of Measuring Fetal Cavum Septum Pellucidum (CSP) Width During Routine Obstetrical Ultrasound for Improving Diagnosis of 22q11.2 Deletion Syndrome: A Case-Control Study","year":2022,"lang":"en","type":"article","venue":"The Application of Clinical Genetics","topic":"Congenital heart defects research","field":"Biochemistry, Genetics and Molecular Biology","cited_by":7,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Manitoba; Children's Hospital Research Institute of Manitoba","funders":"","keywords":"Medicine; Septum pellucidum; Fetus; Anatomy; Pregnancy; Biology","score_opus":0.04746166274589541,"score_gpt":0.35381582216893626,"score_spread":0.30635415942304084,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4287379005","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9914398,0.0008936808,0.005248711,0.000034997345,0.000069097165,0.0020525055,0.00023254614,0.000007985304,0.000020653344],"genre_scores_gemma":[0.9989579,0.00003335744,0.00043920247,0.000011126635,0.00006226157,0.0004041271,0.000024535722,0.000027919035,0.0000395809],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9972085,0.0005116769,0.0011315745,0.0004457812,0.00045296067,0.00024955842],"domain_scores_gemma":[0.99709433,0.0011102944,0.0004995943,0.0008422995,0.0003642089,0.00008927499],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0018043737,0.00014812367,0.00043727594,0.000057946487,0.00016973205,0.000007520652,0.0004189868,0.00010565991,0.000023036173],"category_scores_gemma":[0.0014495782,0.00013493955,0.00029732083,0.0002767688,0.00020839702,0.000003429357,0.00036737788,0.00024175706,7.8284876e-7],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0013174532,0.002796604,0.7031608,0.00045174538,0.00046330295,0.00001199388,0.00025629153,0.0013140524,0.22616112,0.000019884883,0.000019016681,0.06402771],"study_design_scores_gemma":[0.005893467,0.004995643,0.798974,0.000011296485,0.0005174182,0.00023101304,0.0012661149,0.015761241,0.1714877,0.00014110569,0.00034707037,0.00037392366],"about_ca_topic_score_codex":0.000086195636,"about_ca_topic_score_gemma":0.00006687618,"teacher_disagreement_score":0.09581319,"about_ca_system_score_codex":0.00001734089,"about_ca_system_score_gemma":0.00012364265,"threshold_uncertainty_score":0.5502675},"labels":[],"label_agreement":null},{"id":"W4360615761","doi":"10.2147/tacg.s401712","title":"Genetic Loss of Sucrase-Isomaltase Function: Mechanisms, Implications, and Future Perspectives","year":2023,"lang":"en","type":"review","venue":"The Application of Clinical Genetics","topic":"Digestive system and related health","field":"Biochemistry, Genetics and Molecular Biology","cited_by":17,"is_retracted":false,"has_abstract":true,"route_ca_aff":false,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":true,"ca_institutions":"","funders":"Novo Nordisk Foundation Center for Basic Metabolic Research; Novo Nordisk Fonden; Copenhagen Graduate School for Nanoscience and Nanotechnology; Novo Nordisk","keywords":"Function (biology); Loss function; Computational biology; Biology; Evolutionary biology; Medicine; Genetics; Bioinformatics; Gene; Phenotype","score_opus":0.05989780976577334,"score_gpt":0.41838037796824895,"score_spread":0.3584825682024756,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4360615761","genre_codex":"review","genre_gemma":"review","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"review","genre_consensus":"review","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.00050108717,0.99198186,0.0054123937,0.00021498854,0.00018594731,0.00132043,0.00020404076,0.00001713312,0.00016212538],"genre_scores_gemma":[0.0019992273,0.9956115,0.0008157128,0.000039917428,0.0009245534,0.00018194733,0.00019800193,0.00005872934,0.00017045152],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.9971598,0.00036838892,0.0015497953,0.0005659607,0.00017434194,0.00018175103],"domain_scores_gemma":[0.99698836,0.00021984265,0.0013241332,0.0010586751,0.00028875825,0.000120245786],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00082102284,0.00027402723,0.0010071412,0.0000615911,0.000088451634,0.000008032707,0.00043591845,0.0006815854,0.0000052527694],"category_scores_gemma":[0.00008571845,0.00018880956,0.00037404618,0.00029656387,0.0003722644,0.0000013591425,0.0001868956,0.00025904516,0.000022649592],"study_design_candidate":"not_applicable","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.000048724058,0.00021261926,0.00024559145,0.005813354,0.00063576596,4.2398534e-7,0.000040833544,0.000008589401,0.00008251158,0.021766286,0.00073138566,0.9704139],"study_design_scores_gemma":[0.00028186792,0.00044254237,0.0034590971,0.00038836244,0.00083950337,0.000021121237,0.00015639189,0.000008901714,0.0000214269,0.0021371786,0.99200785,0.00023572781],"about_ca_topic_score_codex":0.000008072657,"about_ca_topic_score_gemma":0.0000057383777,"teacher_disagreement_score":0.9912765,"about_ca_system_score_codex":0.000008768671,"about_ca_system_score_gemma":0.00037269233,"threshold_uncertainty_score":0.76994306},"labels":[],"label_agreement":null},{"id":"W4400255781","doi":"10.2147/tacg.s463965","title":"The Diversity of CYP2C19 Polymorphisms in the Thai Population: Implications for Precision Medicine","year":2024,"lang":"en","type":"article","venue":"The Application of Clinical Genetics","topic":"Pharmacogenetics and Drug Metabolism","field":"Pharmacology, Toxicology and Pharmaceutics","cited_by":9,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Ottawa","funders":"Mahidol University; Rangsit University; Thailand Center of Excellence for Life Sciences","keywords":"CYP2C19; Diversity (politics); Precision medicine; Korean population; Genetics; Medicine; Biology; Genotype; Internal medicine; Gene; Sociology; Anthropology","score_opus":0.3070593084405237,"score_gpt":0.5653913490503782,"score_spread":0.25833204060985454,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4400255781","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.89689463,0.01961267,0.016658263,0.059820194,0.0016960787,0.0030212516,0.00024125045,0.000041397794,0.0020142428],"genre_scores_gemma":[0.992614,0.005275815,0.00023744915,0.0010627279,0.0005114075,0.00014710899,0.000030084753,0.000011566281,0.000109881235],"study_design_codex":"design_other","study_design_gemma":"observational","domain_scores_codex":[0.9978452,0.000535975,0.0009950466,0.00023382774,0.0002087954,0.00018120457],"domain_scores_gemma":[0.9920727,0.0068466184,0.00032543848,0.0005503136,0.00014328216,0.00006162667],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0050147,0.00011851392,0.00026053286,0.000044630906,0.00035160818,0.0000096637295,0.0009942255,0.00016477244,0.000026225243],"category_scores_gemma":[0.00027645173,0.00006029386,0.00016357968,0.0003819695,0.0005420254,0.000021038082,0.00021193069,0.00038230958,0.000007796039],"study_design_candidate":"design_other","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00037468594,0.00034226867,0.06621908,0.000054127326,0.00017591943,2.3986664e-7,0.0016273968,0.001371937,0.008391083,0.12854503,0.0072063366,0.7856919],"study_design_scores_gemma":[0.0011084343,0.00015363788,0.44076562,0.000016535909,0.00045151258,0.0000033372803,0.00013153926,0.018276438,0.002317842,0.10495589,0.43169823,0.00012097124],"about_ca_topic_score_codex":0.00003648577,"about_ca_topic_score_gemma":0.000024011824,"teacher_disagreement_score":0.7855709,"about_ca_system_score_codex":0.000009569994,"about_ca_system_score_gemma":0.00005281881,"threshold_uncertainty_score":0.27043214},"labels":[],"label_agreement":null},{"id":"W7116968871","doi":"10.2147/tacg.s549120","title":"A Novel Exon Duplication in the SACS Gene in Charlevoix-Saguenay Ataxia and a Summary of Polish Cases","year":2025,"lang":"en","type":"article","venue":"The Application of Clinical Genetics","topic":"Genetic Neurodegenerative Diseases","field":"Neuroscience","cited_by":0,"is_retracted":false,"has_abstract":true,"route_ca_aff":false,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":true,"ca_institutions":"","funders":"","keywords":"Frameshift mutation; Gene duplication; Exon; Ataxia; Cerebellar ataxia; Mutation; Compound heterozygosity; Gene","score_opus":0.08814800585122207,"score_gpt":0.38788791649475735,"score_spread":0.2997399106435353,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W7116968871","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99418235,0.00047263846,0.0021572164,0.001922506,0.000042091164,0.0009141308,0.0000509267,0.000008060616,0.00025010708],"genre_scores_gemma":[0.99669117,0.0011476915,0.00043029577,0.0014567387,0.000040149243,0.00016506,0.0000066678244,0.00000953113,0.00005271978],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9978312,0.00040275406,0.00094574934,0.0004125099,0.00025151044,0.00015624499],"domain_scores_gemma":[0.9964066,0.002300064,0.00035739574,0.000817455,0.00008100008,0.000037471236],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00079893286,0.00012604546,0.00027747618,0.00009224849,0.000046395497,0.000015122484,0.0006302101,0.00007714852,0.0000020206533],"category_scores_gemma":[0.0014439536,0.00008835532,0.000065911016,0.0006529285,0.00046432056,0.000027089825,0.00015864821,0.00017238127,0.0000022855372],"study_design_candidate":"bench_or_experimental","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00016628196,0.00092650804,0.07963081,0.000069495625,0.000006768817,9.965778e-7,0.00030787624,0.00073104043,0.88830006,0.006898568,0.0002567609,0.022704825],"study_design_scores_gemma":[0.0006997653,0.00008636754,0.6133148,0.000024160985,0.000028166318,0.000003804293,0.00007903346,0.0027216754,0.3799881,0.0017668038,0.0012005058,0.00008680891],"about_ca_topic_score_codex":0.00010998633,"about_ca_topic_score_gemma":0.0001285619,"teacher_disagreement_score":0.533684,"about_ca_system_score_codex":0.000008630333,"about_ca_system_score_gemma":0.000099348035,"threshold_uncertainty_score":0.36030254},"labels":[],"label_agreement":null}]}