{"meta":{"query_hash":"285b48442abe","filters":{"venue":"Annals of Human Genetics"},"cohort_total":65,"direct_labels_cover":0,"predictions_cover":65,"exported":65,"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/285b48442abe","api":"https://metacan.xera.ac/api/v1/cohort?venue=Annals+of+Human+Genetics"},"results":[{"id":"W1480934029","doi":"10.1111/j.1469-1809.2010.00597.x","title":"Joint Identification of Multiple Genetic Variants via Elastic‐Net Variable Selection in a Genome‐Wide Association Analysis","year":2010,"lang":"en","type":"article","venue":"Annals of Human Genetics","topic":"Genetic Associations and Epidemiology","field":"Biochemistry, Genetics and Molecular Biology","cited_by":106,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Emergent BioSolutions (Canada)","funders":"","keywords":"Genome-wide association study; Genetic association; Selection (genetic algorithm); Identification (biology); Biology; Genetics; Computational biology; Replication (statistics); Single-nucleotide polymorphism; Population; Computer science; Gene; Genotype; Artificial intelligence; Medicine","score_opus":0.0215135982691505,"score_gpt":0.28616511804408473,"score_spread":0.26465151977493423,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1480934029","genre_codex":"methods","genre_gemma":"methods","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"methods","genre_consensus":"methods","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.2649126,0.00016217372,0.7337318,0.00018906871,0.000026234615,0.0001754831,0.000072446725,0.00018148813,0.0005486604],"genre_scores_gemma":[0.76604545,0.00011739627,0.23218177,0.000080318074,0.000038791015,0.00030211452,0.0002635043,0.000043326203,0.0009273419],"study_design_codex":"simulation_or_modeling","study_design_gemma":"simulation_or_modeling","domain_scores_codex":[0.9929542,0.0052410704,0.00027283028,0.0007289448,0.00060442596,0.00019860888],"domain_scores_gemma":[0.97871196,0.017857099,0.0009718218,0.0015420376,0.0006793583,0.00023756866],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.020856231,0.0006452768,0.001271628,0.001754282,0.000892721,0.001117443,0.0014687309,0.00072962017,0.0015071622],"category_scores_gemma":[0.030951064,0.0006763612,0.0012991979,0.0017960867,0.0012225384,0.001126751,0.0018463773,0.0012460176,0.00022056575],"study_design_candidate":"simulation_or_modeling","study_design_consensus":"simulation_or_modeling","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0020805236,0.00056612556,0.16586187,0.00017567657,0.0019051343,0.0014906392,0.00044457195,0.5460403,0.013277971,0.023998199,0.00066404114,0.24349497],"study_design_scores_gemma":[0.000097962184,0.00012280076,0.019206421,0.000016791493,0.0002144297,0.00014240613,0.000047468053,0.9661411,0.00141506,0.012152187,0.00039378228,0.00004965429],"about_ca_topic_score_codex":0.0020378346,"about_ca_topic_score_gemma":0.0031223763,"teacher_disagreement_score":0.020856231,"about_ca_system_score_codex":0.00038179822,"about_ca_system_score_gemma":0.0009900169,"threshold_uncertainty_score":0.11029959},"labels":[],"label_agreement":null},{"id":"W1485413733","doi":"10.1111/ahg.12035","title":"Secondary Analysis of Publicly Available Data Reveals Superoxide and Oxygen Radical Pathways are Enriched for Associations Between Type 2 Diabetes and Low‐Frequency Variants","year":2013,"lang":"en","type":"article","venue":"Annals of Human Genetics","topic":"Genetic Associations and Epidemiology","field":"Biochemistry, Genetics and Molecular Biology","cited_by":4,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Simon Fraser University; Child and Family Research Institute; University of British Columbia","funders":"National Institute of Diabetes and Digestive and Kidney Diseases; National Human Genome Research Institute; National Cancer Institute; National Institutes of Health; Simon Fraser University; Natural Sciences and Engineering Research Council of Canada; Broad Institute","keywords":"Type 2 diabetes; False discovery rate; Missing heritability problem; Heritability; Genome-wide association study; Diabetes mellitus; Genetics; Genetic association; Biology; Locus (genetics); Gene; Computational biology; Bioinformatics; Single-nucleotide polymorphism; Genotype; Endocrinology","score_opus":0.08975566211286656,"score_gpt":0.316776296904358,"score_spread":0.22702063479149143,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1485413733","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.8877941,0.0024394365,0.0066589783,0.00076648575,0.00008821982,0.00009458695,0.09900162,0.0013184005,0.0018381734],"genre_scores_gemma":[0.8813296,0.000593614,0.0074523687,0.00036940785,0.00009306182,0.00021464632,0.10896906,0.0002019256,0.0007762606],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9959552,0.0009266321,0.00035381675,0.0017045502,0.000572405,0.00048742688],"domain_scores_gemma":[0.9868997,0.0065568085,0.0030460646,0.0017648899,0.0011950422,0.0005375649],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0035762356,0.0005997502,0.0018545251,0.0026907544,0.00071758474,0.0020259724,0.00057571416,0.0005538521,0.0028097522],"category_scores_gemma":[0.007217943,0.00024031407,0.0021374421,0.0048611136,0.0005968229,0.000578729,0.0013883567,0.0007956321,0.0011420589],"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":[0.0030814768,0.00040785634,0.8782557,0.0017291633,0.003646573,0.0008290266,0.00037130679,0.0012153753,0.061904926,0.0007802548,0.012122221,0.035655957],"study_design_scores_gemma":[0.00008206174,0.00018146288,0.9884162,0.00005332277,0.0007022183,0.00033255207,0.00017287588,0.002241851,0.003684591,0.00082350057,0.0032846418,0.000024802168],"about_ca_topic_score_codex":0.0039573335,"about_ca_topic_score_gemma":0.0078049917,"teacher_disagreement_score":0.0039573335,"about_ca_system_score_codex":0.0005913216,"about_ca_system_score_gemma":0.0012679622,"threshold_uncertainty_score":0.01891315},"labels":[],"label_agreement":null},{"id":"W1490699327","doi":"10.1111/j.1469-1809.2012.00731.x","title":"Combined Polymorphisms in Oxidative Stress Genes Predict Coronary Artery Disease and Oxidative Stress in Coronary Angiography Patients","year":2012,"lang":"en","type":"article","venue":"Annals of Human Genetics","topic":"Atherosclerosis and Cardiovascular Diseases","field":"Immunology and Microbiology","cited_by":23,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"St. Paul's Hospital; University of Toronto; University of British Columbia","funders":"Canadian Institutes of Health Research; Heart and Stroke Foundation of Canada","keywords":"Oxidative stress; Single-nucleotide polymorphism; Coronary artery disease; Genotyping; Haplotype; Linkage disequilibrium; Medicine; Internal medicine; Biomarker; Genotype; Biology; Genetics; Gene","score_opus":0.0260590506160806,"score_gpt":0.25449346252843863,"score_spread":0.22843441191235803,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1490699327","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9995803,0.00007110772,0.000098858865,0.000029774845,0.0000032215767,0.000003102672,0.000033787554,0.000002141637,0.00017764213],"genre_scores_gemma":[0.99962366,0.000035216406,0.0001298642,0.000015192536,0.000010331677,0.0000040953687,0.00006637042,0.0000012977532,0.00011391023],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9996666,0.0001282787,0.00003079669,0.00006881144,0.00005306242,0.000052511637],"domain_scores_gemma":[0.9990088,0.00034915112,0.00026241044,0.000079539284,0.000073941264,0.00022617873],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0005612364,0.00033207546,0.00026949664,0.0005871419,0.0003215668,0.0004597744,0.00020194372,0.00065320544,0.001759112],"category_scores_gemma":[0.0021169067,0.00030368104,0.0003599977,0.00046507915,0.00025906586,0.0001755235,0.0002647023,0.00059821416,0.00022237269],"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":[0.00033791005,0.0000614808,0.9968573,0.000003094754,0.00006067402,0.00012811535,0.000030253526,0.00006355322,0.0013333921,0.00002012427,0.000056366003,0.0010476945],"study_design_scores_gemma":[0.000022796612,0.00017948443,0.9982844,0.0000037100058,0.0000853863,0.00049507595,0.000047033536,0.0005273444,0.00019993473,0.00008381931,0.000066486115,0.000004552978],"about_ca_topic_score_codex":0.001072273,"about_ca_topic_score_gemma":0.0016358193,"teacher_disagreement_score":0.001759112,"about_ca_system_score_codex":0.00011559394,"about_ca_system_score_gemma":0.0001626635,"threshold_uncertainty_score":0.005884826},"labels":[],"label_agreement":null},{"id":"W1499730254","doi":"10.1111/j.1469-1809.2010.00578.x","title":"Association of polymorphisms in the <i>BDNF</i>, <i>DRD1</i> and <i>DRD3</i> genes with tobacco smoking in schizophrenia","year":2010,"lang":"en","type":"article","venue":"Annals of Human Genetics","topic":"Nicotinic Acetylcholine Receptors Study","field":"Biochemistry, Genetics and Molecular Biology","cited_by":60,"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","keywords":"rs6265; Single-nucleotide polymorphism; Haplotype; Nicotine; Addiction; Gene; SNP; Genetics; Association (psychology); Medicine; Internal medicine; Psychology; Biology; Allele; Psychiatry; Genotype","score_opus":0.015741445303953265,"score_gpt":0.28007607972024323,"score_spread":0.26433463441628996,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1499730254","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99963605,0.00009982964,0.00006975901,0.00002559325,0.0000016569511,0.0000020660182,0.000052639494,0.0000014339058,0.000110990644],"genre_scores_gemma":[0.99955887,0.0000756257,0.00015812276,0.000017465502,0.0000038704275,0.0000023224502,0.000077948294,0.0000016568769,0.000104110964],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99974316,0.00008697273,0.000037319493,0.000059425125,0.00004236219,0.0000308195],"domain_scores_gemma":[0.99947304,0.00016272055,0.00019128584,0.00004870684,0.000038450882,0.00008579564],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00041057836,0.0002368558,0.00019397479,0.000401231,0.00024688448,0.00028184376,0.00017900526,0.0002836204,0.0013622034],"category_scores_gemma":[0.0010326073,0.00016421865,0.0002975074,0.0004960967,0.00023029296,0.00008288378,0.00018438871,0.0003502205,0.00015060932],"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":[0.0014837041,0.0001162797,0.967035,0.000022416778,0.0003213348,0.0005450146,0.00017543601,0.00024785975,0.023859318,0.00008541331,0.00012900347,0.005979228],"study_design_scores_gemma":[0.0000386086,0.00014628096,0.99730814,0.0000046956334,0.00010891442,0.00069322356,0.000049587663,0.00027083434,0.0011503733,0.00007503333,0.00014849771,0.000005774494],"about_ca_topic_score_codex":0.0034577653,"about_ca_topic_score_gemma":0.004669424,"teacher_disagreement_score":0.0034577653,"about_ca_system_score_codex":0.00016443722,"about_ca_system_score_gemma":0.00015682033,"threshold_uncertainty_score":0.0068752766},"labels":[],"label_agreement":null},{"id":"W1507546761","doi":"10.1111/j.1469-1809.2010.00599.x","title":"On the Use of Allelic Transmission Rates for Assessing Gene‐by‐Environment Interaction in Case‐Parent Trios","year":2010,"lang":"en","type":"article","venue":"Annals of Human Genetics","topic":"Evolution and Genetic Dynamics","field":"Biochemistry, Genetics and Molecular Biology","cited_by":2,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Simon Fraser University","funders":"","keywords":"Transmission (telecommunications); Penetrance; Genetics; Allele; Pedigree chart; Biology; Statistics; Population; Population stratification; Econometrics; Range (aeronautics); Evolutionary biology; Demography; Gene; Computer science; Mathematics; Genotype; Engineering","score_opus":0.09024440015869163,"score_gpt":0.3732222954338624,"score_spread":0.2829778952751708,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1507546761","genre_codex":"empirical","genre_gemma":"methods","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"methods","genre_consensus":null,"domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.5483569,0.00095708156,0.44207796,0.0017733133,0.00014826504,0.00030095983,0.0006775511,0.00049709354,0.0052108825],"genre_scores_gemma":[0.8720535,0.00032975292,0.12656029,0.00023820125,0.000053684158,0.00019221389,0.00019990608,0.00011557788,0.0002568571],"study_design_codex":"observational","study_design_gemma":"theoretical_or_conceptual","domain_scores_codex":[0.8560466,0.13243768,0.0033810528,0.0039436705,0.003704333,0.00048660277],"domain_scores_gemma":[0.35625494,0.5921842,0.023422306,0.024412937,0.002813667,0.00091190246],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.12788054,0.00079312123,0.0011015162,0.004186945,0.0007730942,0.0025605566,0.0020487558,0.0017431198,0.0022607937],"category_scores_gemma":[0.4460903,0.00059904007,0.0016766886,0.0042314027,0.0038393913,0.003581832,0.0021371809,0.0026813273,0.00031081372],"study_design_candidate":"theoretical_or_conceptual","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0015691147,0.00021785124,0.5513391,0.0007547904,0.0035591996,0.0014248186,0.0070569906,0.069682196,0.0039018462,0.11819379,0.0024484121,0.23985185],"study_design_scores_gemma":[0.0003276127,0.0014498468,0.29642704,0.0007282289,0.0014198212,0.0044144094,0.0024382346,0.44512543,0.009554102,0.23235272,0.00509881,0.00066371885],"about_ca_topic_score_codex":0.0017559163,"about_ca_topic_score_gemma":0.0024655308,"teacher_disagreement_score":0.12788054,"about_ca_system_score_codex":0.000901345,"about_ca_system_score_gemma":0.00064411026,"threshold_uncertainty_score":0.67630506},"labels":[],"label_agreement":null},{"id":"W1509468647","doi":"10.1111/j.1469-1809.2012.00711.x","title":"Familial Clustering Strongly Suggests that the Phenotypic Variation of the 8344 A&gt;G Lys Mitochondrial tRNA Mutation is Encoded in <i>cis</i>","year":2012,"lang":"en","type":"article","venue":"Annals of Human Genetics","topic":"Mitochondrial Function and Pathology","field":"Biochemistry, Genetics and Molecular Biology","cited_by":8,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"McGill University; McGill University Health Centre","funders":"McGill University","keywords":"Heteroplasmy; Lipomatosis; Myoclonic epilepsy; Mitochondrial myopathy; Biology; Genetics; Mitochondrial DNA; Leigh disease; Myopathy; Mutation; Endocrinology; Internal medicine; Epilepsy; Medicine; Gene","score_opus":0.04037736822695204,"score_gpt":0.29346407549067005,"score_spread":0.253086707263718,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1509468647","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99687934,0.0003529474,0.0008427504,0.00012166911,0.000009362558,0.0000110082265,0.00014305764,0.00003402674,0.00160587],"genre_scores_gemma":[0.99897027,0.00016827961,0.00040502066,0.000034153112,0.000017931225,0.000003735419,0.00012679586,0.000007843574,0.00026590645],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9997105,0.00006538041,0.00003798368,0.00011021255,0.000048273403,0.000027623044],"domain_scores_gemma":[0.9989183,0.00028164187,0.00049655477,0.0001143277,0.00007365223,0.00011552917],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00022661644,0.00045946726,0.00043809233,0.000747386,0.00049770024,0.00022960192,0.00024193348,0.0003609847,0.0040788027],"category_scores_gemma":[0.0007053189,0.00012512818,0.00029443286,0.00074407714,0.00059781095,0.00020668993,0.000321435,0.00029598223,0.0005781077],"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":[0.00018075551,0.000065931206,0.8922689,0.00010570368,0.0003215442,0.031394333,0.0006074476,0.00035707428,0.0594983,0.00053967105,0.0005130631,0.014147163],"study_design_scores_gemma":[0.000011553837,0.00022134383,0.8765326,0.000029685234,0.00012527448,0.115503326,0.00053973123,0.00026640104,0.004138123,0.00081040105,0.0017999925,0.000021633263],"about_ca_topic_score_codex":0.0006332962,"about_ca_topic_score_gemma":0.00083055656,"teacher_disagreement_score":0.0040788027,"about_ca_system_score_codex":0.00014936765,"about_ca_system_score_gemma":0.00014217323,"threshold_uncertainty_score":0.013644993},"labels":[],"label_agreement":null},{"id":"W1523558272","doi":"10.1111/j.1469-1809.2007.00350.x","title":"Confidence intervals for candidate gene effects and environmental factors in population‐based association studies of families","year":2007,"lang":"en","type":"article","venue":"Annals of Human Genetics","topic":"Genetic Associations and Epidemiology","field":"Biochemistry, Genetics and Molecular Biology","cited_by":4,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Hospital for Sick Children; University of Toronto; Lunenfeld-Tanenbaum Research Institute; University of Guelph; Eli Lilly (Canada)","funders":"Division of Mathematical Sciences; Canadian Institutes of Health Research","keywords":"Confidence interval; Candidate gene; Population; Genetics; Biology; Association (psychology); Gene; Demography; Statistics; Environmental health; Medicine; Psychology; Mathematics; Sociology","score_opus":0.04337728710745409,"score_gpt":0.35282445390296197,"score_spread":0.3094471667955079,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1523558272","genre_codex":"methods","genre_gemma":"methods","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"methods","genre_consensus":"methods","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.16913761,0.021607146,0.7950566,0.0015137393,0.0005308943,0.0005326323,0.0017167823,0.001622948,0.008281644],"genre_scores_gemma":[0.82343805,0.0026702818,0.16915582,0.00044510642,0.00033180686,0.0010088799,0.0018784949,0.00028187974,0.0007897457],"study_design_codex":"design_other","study_design_gemma":"simulation_or_modeling","domain_scores_codex":[0.88539857,0.091275215,0.00471986,0.0068497807,0.010556787,0.0011997091],"domain_scores_gemma":[0.2397183,0.72032845,0.014403895,0.018690437,0.0054764375,0.0013824838],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.14144781,0.0012057257,0.003130141,0.0079244645,0.0010850199,0.0037193368,0.0057751765,0.004367235,0.0049955533],"category_scores_gemma":[0.569837,0.00089828676,0.0032371308,0.005839136,0.004541074,0.0036215202,0.0042221146,0.0046183015,0.00052647153],"study_design_candidate":"simulation_or_modeling","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.009303983,0.00051782833,0.11351035,0.004589996,0.014087086,0.0032427511,0.0034113955,0.19203366,0.0027115438,0.29540193,0.008417277,0.35277218],"study_design_scores_gemma":[0.0013363569,0.0021323473,0.124847054,0.003463629,0.0034200393,0.0048106946,0.0013559446,0.5342977,0.005551669,0.29828262,0.019836584,0.0006652283],"about_ca_topic_score_codex":0.004480368,"about_ca_topic_score_gemma":0.0018471499,"teacher_disagreement_score":0.14144781,"about_ca_system_score_codex":0.0012709354,"about_ca_system_score_gemma":0.0012147658,"threshold_uncertainty_score":0.7480565},"labels":[],"label_agreement":null},{"id":"W1524575989","doi":"10.1046/j.1529-8817.2003.00124.x","title":"Linkage Disequilibrium and Haplotype Architecture for two ABC Transporter Genes (<i>ABCC1</i> and <i>ABCG2</i>) in Chinese Population: Implications for Pharmacogenomic Association Studies","year":2004,"lang":"en","type":"article","venue":"Annals of Human Genetics","topic":"Drug Transport and Resistance Mechanisms","field":"Medicine","cited_by":26,"is_retracted":false,"has_abstract":true,"route_ca_aff":false,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"","funders":"Institute of Genetics; Fudan University","keywords":"Linkage disequilibrium; Genetics; Haplotype; Biology; Single-nucleotide polymorphism; Genetic association; Locus (genetics); Gene; Association mapping; ABCC1; Tag SNP; Allele; ATP-binding cassette transporter; Genotype; Transporter","score_opus":0.05405978089511921,"score_gpt":0.384106072438172,"score_spread":0.3300462915430528,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1524575989","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9992618,0.00008687367,0.00035385368,0.000031989406,0.000001405314,0.000005163641,0.00006479706,0.0000020941534,0.00019198789],"genre_scores_gemma":[0.99945587,0.00006137826,0.00021307125,0.000011216234,0.000005124159,0.0000069735556,0.0001275301,0.0000018674765,0.000116864925],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99943346,0.00017963824,0.000043383166,0.00018975264,0.00007266962,0.00008103172],"domain_scores_gemma":[0.9992366,0.00029455387,0.00017628548,0.000105145176,0.000074129435,0.00011337105],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00091276073,0.00017013744,0.00037002467,0.0011734315,0.00054709817,0.00033919135,0.00020930174,0.00021303701,0.0013760856],"category_scores_gemma":[0.001693467,0.00015059009,0.0002794064,0.0013422921,0.0007407566,0.00022409392,0.0002698517,0.00022932996,0.00011732856],"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":[0.00037842433,0.000044283166,0.9638431,0.000027725893,0.0002147764,0.00062928,0.001153371,0.00088876014,0.018254768,0.00081357575,0.00014179699,0.013610154],"study_design_scores_gemma":[0.000027293003,0.00007602973,0.996999,0.0000035875066,0.000076561984,0.0003755477,0.00012784576,0.0010821845,0.00049346907,0.00050303416,0.0002249385,0.000010371069],"about_ca_topic_score_codex":0.010532043,"about_ca_topic_score_gemma":0.011301376,"teacher_disagreement_score":0.010532043,"about_ca_system_score_codex":0.00042791752,"about_ca_system_score_gemma":0.00042239533,"threshold_uncertainty_score":0.020941496},"labels":[],"label_agreement":null},{"id":"W1536982521","doi":"10.1111/ahg.12077","title":"Global Genetic Architecture of an Erythroid Quantitative Trait Locus,<i>HMIP-2</i>","year":2014,"lang":"en","type":"article","venue":"Annals of Human Genetics","topic":"Hemoglobinopathies and Related Disorders","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":"McGill University","funders":"National Institutes of Health; University of Oxford; King's College London; Wellcome Trust; British Heart Foundation; Foreign and Commonwealth Office; Medical Research Council; British Society for Haematology; Commonwealth Scholarship Commission; National Institute for Health and Care Research","keywords":"Biology; Genetics; Locus (genetics); Haplotype; Allele; Fetal hemoglobin; Population; Quantitative trait locus; Expression quantitative trait loci; Genetic architecture; Evolutionary biology; Gene; Genotype; Single-nucleotide polymorphism; Fetus","score_opus":0.030926845422893486,"score_gpt":0.32843555043613365,"score_spread":0.29750870501324017,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1536982521","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99752384,0.000087900444,0.0007953426,0.000027209366,0.000001991727,0.000004895942,0.0011855873,0.00001821198,0.00035502767],"genre_scores_gemma":[0.9980647,0.0000538739,0.00051180134,0.000020239564,0.0000039179913,0.0000064054952,0.0011283825,0.000011766271,0.00019882794],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9995901,0.00008653139,0.000020937861,0.0002300977,0.000034246503,0.000038144335],"domain_scores_gemma":[0.999666,0.00009927305,0.00012088852,0.000043404933,0.000022029675,0.000048452926],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00034638483,0.00018674285,0.00026699615,0.00074255595,0.00018459227,0.00034744383,0.00020255368,0.00019376793,0.002111413],"category_scores_gemma":[0.00054700696,0.00011540439,0.00027265484,0.0008906628,0.00024780256,0.00012743541,0.00038564668,0.0002499531,0.00016610972],"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":[0.0007969863,0.00005542827,0.8333938,0.00006702384,0.00087198627,0.0005168856,0.0006449325,0.0008969342,0.14162019,0.0007053776,0.0006377274,0.019792708],"study_design_scores_gemma":[0.000009379334,0.000047444046,0.9974245,0.0000058683627,0.000078733996,0.00030630032,0.000050183018,0.00062495033,0.0007947008,0.00015723609,0.00049513584,0.000005554179],"about_ca_topic_score_codex":0.0023540223,"about_ca_topic_score_gemma":0.0031752505,"teacher_disagreement_score":0.0023540223,"about_ca_system_score_codex":0.0001346449,"about_ca_system_score_gemma":0.00013577948,"threshold_uncertainty_score":0.007063329},"labels":[],"label_agreement":null},{"id":"W1538799821","doi":"10.1111/ahg.12017","title":"A Novel Mutation in <i>FGD4/FRABIN</i> Causes Charcot Marie Tooth Disease Type 4H in Patients from a Consanguineous Tunisian Family","year":2013,"lang":"en","type":"article","venue":"Annals of Human Genetics","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":19,"is_retracted":false,"has_abstract":true,"route_ca_aff":false,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"","funders":"Agence Universitaire de la Francophonie","keywords":"Consanguinity; Genetic heterogeneity; Frameshift mutation; Genetics; Medicine; Hereditary motor and sensory neuropathy; Founder effect; Consanguineous Marriage; Mutation; Phenotype; Disease; Tooth disease; Age of onset; Chinese family; Biology; Genotype; Gene; Pathology; Haplotype","score_opus":0.0888000202915497,"score_gpt":0.3019097663530389,"score_spread":0.2131097460614892,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1538799821","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9990476,0.00016934637,0.0001764013,0.00009046874,0.0000103647235,0.00001443264,0.00006424647,0.000014350812,0.00041284304],"genre_scores_gemma":[0.99916244,0.00009087781,0.00022793011,0.000097283664,0.000018590905,0.000006189599,0.000055684246,0.000006124832,0.0003348979],"study_design_codex":"case_report","study_design_gemma":"observational","domain_scores_codex":[0.99974924,0.000033929344,0.000029144063,0.00008036106,0.000043769116,0.00006356065],"domain_scores_gemma":[0.99973685,0.000060765895,0.00009229393,0.000013580432,0.000023112794,0.000073470525],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0001659133,0.0011398352,0.00040910873,0.0010239235,0.0012788057,0.00042673352,0.00047070035,0.0008681158,0.0015148369],"category_scores_gemma":[0.0009446888,0.00041790755,0.00044643943,0.0007404689,0.00067992357,0.00020903432,0.00046692014,0.00044523622,0.00019954602],"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":[0.00067067926,0.00021625223,0.38422,0.00013241112,0.0002240905,0.53872794,0.0032764615,0.00043583618,0.051794183,0.00029424235,0.0010604995,0.018947434],"study_design_scores_gemma":[0.00012842136,0.0004251979,0.4663179,0.000053623102,0.0001987079,0.52109736,0.000990282,0.0008849838,0.006361458,0.00017856136,0.0033014754,0.000062106614],"about_ca_topic_score_codex":0.014819091,"about_ca_topic_score_gemma":0.012477396,"teacher_disagreement_score":0.014819091,"about_ca_system_score_codex":0.0008773454,"about_ca_system_score_gemma":0.0004234387,"threshold_uncertainty_score":0.029465675},"labels":[],"label_agreement":null},{"id":"W1546697183","doi":"10.1111/j.1469-1809.2009.00552.x","title":"Attributing Hardy‐Weinberg Disequilibrium to Population Stratification and Genetic Association in Case‐Control Studies","year":2009,"lang":"en","type":"article","venue":"Annals of Human Genetics","topic":"Genetic Associations and Epidemiology","field":"Biochemistry, Genetics and Molecular Biology","cited_by":18,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Toronto; Dalhousie University","funders":"","keywords":"Population stratification; Disequilibrium; Linkage disequilibrium; Biology; Genetic association; Population; Genetic model; Genetics; Locus (genetics); Statistics; Genotype; Evolutionary biology; Single-nucleotide polymorphism; Mathematics; Demography; Gene; Medicine","score_opus":0.05846606092478839,"score_gpt":0.3672563119593728,"score_spread":0.3087902510345844,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1546697183","genre_codex":"methods","genre_gemma":"methods","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"methods","genre_consensus":"methods","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.041553892,0.0008828382,0.9552548,0.00039182472,0.00022385344,0.00049590674,0.000080438964,0.00024894308,0.0008676715],"genre_scores_gemma":[0.5533123,0.0008132217,0.44253013,0.0004511668,0.000280185,0.0015587283,0.00019203033,0.00015742822,0.0007047656],"study_design_codex":"observational","study_design_gemma":"theoretical_or_conceptual","domain_scores_codex":[0.78437537,0.19026399,0.008578874,0.007883472,0.007974913,0.000923394],"domain_scores_gemma":[0.62357885,0.3357484,0.012952169,0.022948876,0.003825054,0.0009467451],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.18008429,0.0011588064,0.0029392836,0.0042102905,0.0017148245,0.0026655684,0.0039915955,0.0021085516,0.0015119014],"category_scores_gemma":[0.36018813,0.0014669878,0.0015974888,0.0055305418,0.0063321134,0.003505998,0.0032103106,0.003398038,0.00025953556],"study_design_candidate":"theoretical_or_conceptual","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.001333808,0.00043694128,0.41835406,0.0017474,0.0046202163,0.0031323137,0.01007556,0.04448581,0.0036797565,0.105549395,0.0045515914,0.40203318],"study_design_scores_gemma":[0.00049953535,0.0016594538,0.14749764,0.00083799683,0.0018469375,0.003995374,0.0017632797,0.39722353,0.00391089,0.42976475,0.010514904,0.00048565862],"about_ca_topic_score_codex":0.0035938655,"about_ca_topic_score_gemma":0.004676803,"teacher_disagreement_score":0.18008429,"about_ca_system_score_codex":0.0012309884,"about_ca_system_score_gemma":0.0021800594,"threshold_uncertainty_score":0.9523881},"labels":[],"label_agreement":null},{"id":"W1561767136","doi":"10.1111/ahg.12002","title":"Genotype‐Based Association Analysis Using Discordant Pairs: A Penetrance Odds Ratio Approach","year":2013,"lang":"en","type":"article","venue":"Annals of Human Genetics","topic":"Genetic Associations and Epidemiology","field":"Biochemistry, Genetics and Molecular Biology","cited_by":1,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Toronto; Dalhousie University","funders":"Natural Sciences and Engineering Research Council of Canada","keywords":"McNemar's test; Odds ratio; Statistics; Score test; Penetrance; Likelihood-ratio test; Genetic association; Genotype; Biology; Mathematics; Genetics; Single-nucleotide polymorphism","score_opus":0.05979904525934441,"score_gpt":0.327271996486529,"score_spread":0.26747295122718456,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1561767136","genre_codex":"methods","genre_gemma":"methods","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"methods","genre_consensus":"methods","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.057909846,0.00033652413,0.9399202,0.00017065732,0.00003015868,0.00018808738,0.00020118571,0.00030683272,0.00093645026],"genre_scores_gemma":[0.6180124,0.0002967475,0.37998173,0.0001277352,0.000065416694,0.00042438577,0.00029785707,0.00007830369,0.00071536476],"study_design_codex":"design_other","study_design_gemma":"theoretical_or_conceptual","domain_scores_codex":[0.97174656,0.02275591,0.0008523762,0.0025481945,0.0018334896,0.00026347028],"domain_scores_gemma":[0.92648065,0.06558651,0.0029001096,0.0039682845,0.0007525559,0.0003119543],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.024380825,0.0011520386,0.002041348,0.0043228036,0.00047550493,0.0014643337,0.0031263386,0.0013410571,0.0018863282],"category_scores_gemma":[0.09371419,0.00072508794,0.0013979179,0.0023494354,0.0014931748,0.0019313056,0.0019666315,0.0015576213,0.0004616602],"study_design_candidate":"theoretical_or_conceptual","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0024075548,0.00059084524,0.25577214,0.00092120457,0.004205615,0.007167756,0.0016998574,0.13839144,0.009197868,0.1547949,0.002580445,0.4222704],"study_design_scores_gemma":[0.00028999455,0.0011820775,0.026375853,0.000095692456,0.00075272756,0.00937961,0.000275341,0.79035676,0.0039555402,0.1640032,0.0031925621,0.00014060555],"about_ca_topic_score_codex":0.0005160757,"about_ca_topic_score_gemma":0.00040314207,"teacher_disagreement_score":0.024380825,"about_ca_system_score_codex":0.0002853356,"about_ca_system_score_gemma":0.00048375683,"threshold_uncertainty_score":0.12893963},"labels":[],"label_agreement":null},{"id":"W1569031808","doi":"10.1111/ahg.12125","title":"Leveling the Playing Field in Homozygosity Mapping Using Map Distances","year":2015,"lang":"en","type":"article","venue":"Annals of Human Genetics","topic":"Genetic Mapping and Diversity in Plants and Animals","field":"Biochemistry, Genetics and Molecular Biology","cited_by":1,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"McGill University and Génome Québec Innovation Centre","funders":"National Natural Science Foundation of China","keywords":"Runs of Homozygosity; Disease gene identification; Field (mathematics); Biology; Genetics; Mathematics; Mutation; Genotype","score_opus":0.183744730824747,"score_gpt":0.3411697367015735,"score_spread":0.15742500587682653,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1569031808","genre_codex":"methods","genre_gemma":"methods","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"methods","genre_consensus":"methods","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.08188212,0.010783874,0.8852278,0.0061937594,0.0008039197,0.00012896382,0.00042001982,0.00074901903,0.013810482],"genre_scores_gemma":[0.54333675,0.0035616886,0.44726905,0.001033596,0.00067038246,0.0002368801,0.00029559428,0.0005478987,0.0030481536],"study_design_codex":"design_other","study_design_gemma":"theoretical_or_conceptual","domain_scores_codex":[0.9672618,0.025444925,0.00080520543,0.0025848406,0.003467035,0.00043616362],"domain_scores_gemma":[0.897681,0.08852493,0.0030390676,0.006383724,0.0032489917,0.0011223247],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.026112052,0.001173507,0.0023098686,0.0057412926,0.0016051128,0.0057050334,0.0030176095,0.0017383249,0.004468257],"category_scores_gemma":[0.13002615,0.0009062401,0.0009573874,0.0067217574,0.0063565494,0.0069454196,0.0055753603,0.0045539904,0.001186001],"study_design_candidate":"theoretical_or_conceptual","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0008233012,0.00010958479,0.05323085,0.0020947743,0.0009912581,0.00061474054,0.0033013306,0.03937184,0.011507617,0.3537227,0.009738984,0.5244931],"study_design_scores_gemma":[0.000115438546,0.00033828212,0.03517487,0.0006132939,0.00024950638,0.0011182693,0.0015700008,0.09448166,0.007981038,0.82198495,0.03601636,0.00035634192],"about_ca_topic_score_codex":0.0024642046,"about_ca_topic_score_gemma":0.0026185275,"teacher_disagreement_score":0.026112052,"about_ca_system_score_codex":0.0012461666,"about_ca_system_score_gemma":0.0008763224,"threshold_uncertainty_score":0.13809538},"labels":[],"label_agreement":null},{"id":"W1572913144","doi":"10.1111/j.1469-1809.2011.00648.x","title":"From Eugenics to Patents: Genetics, Law, and Human Rights","year":2011,"lang":"en","type":"review","venue":"Annals of Human Genetics","topic":"Medical History and Research","field":"Arts and Humanities","cited_by":19,"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":"Eugenics; Law; Genetics; Political science; Sociology; Biology","score_opus":0.36965629696858715,"score_gpt":0.40519906728520927,"score_spread":0.03554277031662212,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1572913144","genre_codex":"commentary","genre_gemma":"review","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"review","genre_consensus":null,"domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.0051343692,0.13208374,0.008789975,0.6138207,0.005049232,0.00002526262,0.00010815215,0.00008574792,0.23490287],"genre_scores_gemma":[0.49243855,0.110353306,0.005023177,0.30033648,0.023476947,0.00015947143,0.00016269054,0.0001573744,0.067891985],"study_design_codex":"theoretical_or_conceptual","study_design_gemma":"not_applicable","domain_scores_codex":[0.98963773,0.005047999,0.00033560712,0.0010924113,0.0028897654,0.0009964823],"domain_scores_gemma":[0.984379,0.012596077,0.0007407504,0.00072585343,0.0009677076,0.0005905929],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.010244022,0.000754684,0.0009400939,0.0019508852,0.0057555567,0.013239176,0.0015142859,0.017680775,0.010597793],"category_scores_gemma":[0.025800822,0.0003746761,0.00045261474,0.0023582613,0.0473461,0.018072834,0.0050358293,0.01683746,0.001722736],"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":[0.000007444731,0.0000069453563,0.00007391359,0.000026734035,0.0000027003275,0.00007187451,0.00040077217,0.00007266343,0.000028772112,0.97435874,0.01715896,0.0077903867],"study_design_scores_gemma":[0.000011201962,0.000013356163,0.00012850274,0.00029561986,0.000003581151,0.00014899402,0.00035962975,0.00010401558,0.00005297721,0.9010251,0.09784163,0.000015418203],"about_ca_topic_score_codex":0.0070697176,"about_ca_topic_score_gemma":0.00682199,"teacher_disagreement_score":0.017680775,"about_ca_system_score_codex":0.008878225,"about_ca_system_score_gemma":0.007785014,"threshold_uncertainty_score":0.06441635},"labels":[],"label_agreement":null},{"id":"W1578854495","doi":"10.1111/j.1469-1809.2007.00414.x","title":"Differential Y‐chromosome Anatolian Influences on the Greek and Cretan Neolithic","year":2008,"lang":"en","type":"article","venue":"Annals of Human Genetics","topic":"Forensic and Genetic Research","field":"Biochemistry, Genetics and Molecular Biology","cited_by":78,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"McMaster University","funders":"","keywords":"Haplogroup; Geography; Mesolithic; Ancient history; Bronze Age; Mainland; Archaeology; History; Biology; Haplotype; Genotype","score_opus":0.07382582546926773,"score_gpt":0.33826444488180096,"score_spread":0.2644386194125332,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1578854495","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.998195,0.00015739312,0.000026326545,0.00002445491,0.0000011327057,0.0000018697384,0.000047270605,0.0000015337234,0.001545024],"genre_scores_gemma":[0.99904877,0.000125565,0.000038047474,0.000013129434,0.0000014630125,0.0000022179722,0.00009144253,0.0000034540271,0.000675965],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9998543,0.000035746765,0.000010086415,0.000046586127,0.00001741042,0.000035756588],"domain_scores_gemma":[0.9997913,0.000037983747,0.0000799232,0.000018895336,0.000041931773,0.000029929073],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00020473028,0.00014519303,0.00012346967,0.0010763397,0.0002118492,0.0006121627,0.00018268719,0.0001476169,0.0020916893],"category_scores_gemma":[0.0005709896,0.00007688326,0.00011040317,0.0010402863,0.00045140611,0.00019126746,0.0005677996,0.0001313111,0.00023159674],"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":[0.00054474187,0.000035886165,0.9185747,0.00006617279,0.00018730361,0.0010100742,0.008026614,0.0002119408,0.028286198,0.0016237695,0.0002792003,0.04115332],"study_design_scores_gemma":[0.000002523223,0.000011543507,0.9977112,0.000009526105,0.000007905836,0.00014194877,0.0008787689,0.000030316918,0.00021342002,0.000050010516,0.0009408261,0.0000020094378],"about_ca_topic_score_codex":0.009292937,"about_ca_topic_score_gemma":0.02613427,"teacher_disagreement_score":0.009292937,"about_ca_system_score_codex":0.00036622156,"about_ca_system_score_gemma":0.0002379282,"threshold_uncertainty_score":0.018477678},"labels":[],"label_agreement":null},{"id":"W1592828382","doi":"10.1111/j.1469-1809.2010.00608.x","title":"Contrasting Patterns of Nuclear and mtDNA Diversity in Native American Populations","year":2010,"lang":"en","type":"article","venue":"Annals of Human Genetics","topic":"Forensic and Genetic Research","field":"Biochemistry, Genetics and Molecular Biology","cited_by":60,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Université de Montréal; Centre Hospitalier Universitaire Sainte-Justine","funders":"","keywords":"Population; Divergence (linguistics); Geography; Evolutionary biology; Autosome; Effective population size; Biology; Ecology; Genetic diversity; Demography; Chromosome; Genetics","score_opus":0.07581676837165921,"score_gpt":0.36535095047520283,"score_spread":0.28953418210354365,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1592828382","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9997613,0.000045009634,0.000033637403,0.00000565498,2.3541597e-7,4.5885287e-7,0.000019452727,9.203302e-7,0.00013337364],"genre_scores_gemma":[0.9996511,0.000048428872,0.00011065885,0.000007866785,0.0000012774601,0.0000017596547,0.00009812054,8.680753e-7,0.00007991221],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99976104,0.00006486338,0.000017632427,0.000080766295,0.000044359087,0.00003138117],"domain_scores_gemma":[0.9997037,0.00006401605,0.00007086674,0.000025196967,0.0000864307,0.000049756574],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.000278276,0.000083774146,0.00014839096,0.0009414604,0.00038636624,0.00052607124,0.0001307541,0.0001218795,0.0005307328],"category_scores_gemma":[0.0008172853,0.00009192233,0.000092674236,0.0007420473,0.0005081495,0.00016672318,0.00035435258,0.0001573995,0.000059842427],"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":[0.00020400785,0.000044169592,0.9606948,0.000024371237,0.00014075098,0.00014675634,0.0032207961,0.00016570702,0.024412015,0.00017909819,0.00006799876,0.010699553],"study_design_scores_gemma":[0.00000265594,0.000027217347,0.99843425,0.0000027686183,0.000014908771,0.0002127737,0.00068858545,0.00010948233,0.00026726234,0.000074785385,0.00016167745,0.0000037571638],"about_ca_topic_score_codex":0.005480834,"about_ca_topic_score_gemma":0.014471261,"teacher_disagreement_score":0.005480834,"about_ca_system_score_codex":0.00018504675,"about_ca_system_score_gemma":0.00016187454,"threshold_uncertainty_score":0.010897875},"labels":[],"label_agreement":null},{"id":"W1593861276","doi":"10.1111/j.1469-1809.2010.00606.x","title":"Association of Linear Growth Impairment in Pediatric Crohn's Disease and a Known Height Locus: A Pilot Study","year":2010,"lang":"en","type":"article","venue":"Annals of Human Genetics","topic":"Inflammatory Bowel Disease","field":"Biochemistry, Genetics and Molecular Biology","cited_by":27,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Montreal Heart Institute","funders":"NIH Clinical Center; National Institute of Diabetes and Digestive and Kidney Diseases; National Center for Research Resources; Koninklijke Nederlandse Akademie van Wetenschappen; Harvard Catalyst","keywords":"Transmission disequilibrium test; Allele; Locus (genetics); Genetics; Etiology; Short stature; Disease; Proband; Medicine; Biology; Internal medicine; Gene; Haplotype; Mutation","score_opus":0.01607983039395603,"score_gpt":0.28398226437541335,"score_spread":0.2679024339814573,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1593861276","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9996581,0.00008300823,0.00008520653,0.000008234305,0.0000015058007,0.000004714384,0.00007760481,0.0000020309562,0.000079609046],"genre_scores_gemma":[0.99961865,0.000047203277,0.00013129464,0.00000850974,0.000005123806,0.0000065529794,0.00011847758,0.0000016217379,0.00006257045],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9995376,0.0001705786,0.000037108624,0.00013638337,0.00006325249,0.00005518406],"domain_scores_gemma":[0.9979473,0.0008046949,0.0005420849,0.0002407346,0.00016344672,0.000301785],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0007317659,0.00042977164,0.00040223918,0.00044040682,0.00031213276,0.00036956248,0.00028710387,0.00036395472,0.0016726204],"category_scores_gemma":[0.0019994474,0.00022509867,0.0003858868,0.0006824775,0.00033450045,0.00021865821,0.0003344574,0.000413485,0.00017301872],"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":[0.00065956917,0.0001082203,0.9962424,0.000013192421,0.000082944214,0.00037190353,0.0000878511,0.000036126847,0.00081503496,0.000015050994,0.000045965608,0.0015217009],"study_design_scores_gemma":[0.000057309026,0.0012842257,0.99648833,0.0000052154314,0.00008048118,0.0013725286,0.0001149419,0.00024789994,0.00017290303,0.000016519705,0.0001564801,0.0000031957484],"about_ca_topic_score_codex":0.002213481,"about_ca_topic_score_gemma":0.0020270515,"teacher_disagreement_score":0.002213481,"about_ca_system_score_codex":0.00018631494,"about_ca_system_score_gemma":0.00023132045,"threshold_uncertainty_score":0.0055955052},"labels":[],"label_agreement":null},{"id":"W1658308648","doi":"10.1111/j.1469-1809.2011.00646.x","title":"Association of SNP rs17465637 on Chromosome 1q41 and rs599839 on 1p13.3 with Myocardial Infarction in an American Caucasian Population","year":2011,"lang":"en","type":"article","venue":"Annals of Human Genetics","topic":"Nuclear Receptors and Signaling","field":"Neuroscience","cited_by":50,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Emergent BioSolutions (Canada)","funders":"National Heart, Lung, and Blood Institute","keywords":"Single-nucleotide polymorphism; Genome-wide association study; SNP; Genetic association; Population; Medicine; Minor allele frequency; Internal medicine; Genetics; Biology; Oncology; Genotype; Gene","score_opus":0.0987907508317559,"score_gpt":0.3233655542397669,"score_spread":0.22457480340801098,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1658308648","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9984268,0.00038459952,0.00018969821,0.00011332034,0.000015312244,0.000009763296,0.00033966594,0.000009732906,0.00051111757],"genre_scores_gemma":[0.9985922,0.00014725419,0.00028929242,0.000056171655,0.0000322775,0.000016493756,0.00038224677,0.0000068604245,0.00047723262],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9994911,0.000109628956,0.0000438055,0.00020987634,0.000088946676,0.000056517787],"domain_scores_gemma":[0.9994319,0.00014554895,0.00022654183,0.000060979826,0.000038372375,0.00009672304],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0005635158,0.000486273,0.00046072094,0.00089544285,0.0007457262,0.00048999465,0.00034005454,0.0007433433,0.00358165],"category_scores_gemma":[0.0015082173,0.00026434645,0.0005466877,0.0014905602,0.00040177983,0.0001683165,0.00028471494,0.00048420363,0.00039575095],"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":[0.00254245,0.00014030248,0.9649483,0.000054722983,0.0005790864,0.002420362,0.00043117447,0.00014050413,0.02003691,0.00023733317,0.00069869985,0.0077702426],"study_design_scores_gemma":[0.000060728853,0.00011768689,0.9968983,0.0000071996587,0.00016184941,0.001265835,0.00008508417,0.00021474982,0.00036322232,0.00019803067,0.00061839155,0.000008886738],"about_ca_topic_score_codex":0.0056439047,"about_ca_topic_score_gemma":0.0057785697,"teacher_disagreement_score":0.0056439047,"about_ca_system_score_codex":0.00021939121,"about_ca_system_score_gemma":0.00029519314,"threshold_uncertainty_score":0.011981785},"labels":[],"label_agreement":null},{"id":"W1815418137","doi":"10.1111/j.1469-1809.2007.00404.x","title":"Testing for Equality of Standardized Composite Measures of Linkage Disequilibrium","year":2007,"lang":"en","type":"article","venue":"Annals of Human Genetics","topic":"Genetic Associations and Epidemiology","field":"Biochemistry, Genetics and Molecular Biology","cited_by":3,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Toronto; Dalhousie University","funders":"Natural Sciences and Engineering Research Council of Canada","keywords":"Linkage disequilibrium; Disequilibrium; Consistency (knowledge bases); Variance (accounting); Measure (data warehouse); Linkage (software); Mathematics; Statistics; Composite number; Econometrics; Genetics; Biology; Genotype; Computer science; Algorithm; Economics; Medicine; Haplotype; Discrete mathematics; Data mining; Accounting","score_opus":0.14707529875554343,"score_gpt":0.39468850490243945,"score_spread":0.24761320614689603,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1815418137","genre_codex":"methods","genre_gemma":"methods","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"methods","genre_consensus":"methods","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.34643018,0.00059641915,0.63959086,0.00052703626,0.00027411192,0.00046042431,0.0015864754,0.00032584224,0.010208582],"genre_scores_gemma":[0.86340064,0.00016545597,0.13304144,0.0002710595,0.000091971015,0.00096077955,0.0013514011,0.000116231335,0.0006010043],"study_design_codex":"observational","study_design_gemma":"theoretical_or_conceptual","domain_scores_codex":[0.9091254,0.051637262,0.0053661494,0.017107708,0.014864072,0.0018993831],"domain_scores_gemma":[0.62640625,0.3195334,0.013172486,0.02845578,0.010698263,0.0017338477],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.07271769,0.0007453784,0.0021328614,0.0034185527,0.0009232254,0.0036969027,0.0021207025,0.0016109577,0.005150575],"category_scores_gemma":[0.34061632,0.00052340265,0.0015848351,0.003431428,0.0057493364,0.004163179,0.0041256,0.0025135607,0.0005206808],"study_design_candidate":"theoretical_or_conceptual","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0025674063,0.00036138116,0.36851498,0.0012308703,0.0038162563,0.0012258266,0.0053881006,0.01884127,0.011049698,0.3209171,0.0039322884,0.26215482],"study_design_scores_gemma":[0.00053876586,0.0024196072,0.24973404,0.00035182558,0.00068893045,0.0026438634,0.0016186632,0.11741261,0.012558614,0.59855235,0.01307161,0.00040909532],"about_ca_topic_score_codex":0.0005842402,"about_ca_topic_score_gemma":0.00041871885,"teacher_disagreement_score":0.07271769,"about_ca_system_score_codex":0.0008862945,"about_ca_system_score_gemma":0.0013117478,"threshold_uncertainty_score":0.3845725},"labels":[],"label_agreement":null},{"id":"W1845049219","doi":"10.1111/j.1469-1809.2010.00617.x","title":"When Genetics and Genealogies Tell Different Stories-Maternal Lineages in Gaspesia","year":2010,"lang":"en","type":"article","venue":"Annals of Human Genetics","topic":"Forensic and Genetic Research","field":"Biochemistry, Genetics and Molecular Biology","cited_by":17,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":true,"ca_institutions":"Université du Québec à Chicoutimi; Université de Montréal; Centre Hospitalier Universitaire Sainte-Justine","funders":"","keywords":"Genealogy; Population; Evolutionary biology; Peninsula; Ancient DNA; Consistency (knowledge bases); Native american; Limiting; Genetic data; Biology; Population genetics; Geography; Ethnology; Demography; History; Ecology; Sociology","score_opus":0.04740267678949312,"score_gpt":0.3494371286052296,"score_spread":0.30203445181573646,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1845049219","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99589914,0.0006542396,0.00080357346,0.0008122126,0.000010931839,0.0000022537322,0.000072124,0.000011854026,0.0017336325],"genre_scores_gemma":[0.9990539,0.00022404102,0.00042269245,0.000071730836,0.000008091521,0.0000019262257,0.000054954322,0.000004408548,0.00015821101],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99936014,0.00033873037,0.000033334767,0.00014190457,0.000064076004,0.00006180268],"domain_scores_gemma":[0.99748707,0.0013686835,0.00061298156,0.00027152698,0.00016136242,0.00009831861],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0019430141,0.00016841781,0.00018278703,0.0012913493,0.0006199669,0.0017102853,0.00041150197,0.00054799614,0.000870173],"category_scores_gemma":[0.008994014,0.00014244014,0.000111518806,0.0011959882,0.002660404,0.0014099127,0.0007263581,0.00048363145,0.0000904379],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":true,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0005368194,0.000032068787,0.83190435,0.000108153436,0.0002582267,0.0027951335,0.050656598,0.0021191475,0.010127403,0.027140517,0.000795873,0.07352572],"study_design_scores_gemma":[0.000019186296,0.000088931774,0.90117246,0.00013100891,0.00016812641,0.0027022914,0.03334333,0.0035810005,0.0023248522,0.045602962,0.010791428,0.00007435158],"about_ca_topic_score_codex":0.00442153,"about_ca_topic_score_gemma":0.007803131,"teacher_disagreement_score":0.99557847,"about_ca_system_score_codex":0.0010177555,"about_ca_system_score_gemma":0.0005570549,"threshold_uncertainty_score":0.010275722},"labels":[],"label_agreement":null},{"id":"W1904831760","doi":"10.1111/ahg.12021","title":"Genome‐Wide Association Study of Pre‐Eclampsia Detects Novel Maternal Single Nucleotide Polymorphisms and Copy‐Number Variants in Subsets of the Hyperglycemia and Adverse Pregnancy Outcome (HAPO) Study Cohort","year":2013,"lang":"en","type":"article","venue":"Annals of Human Genetics","topic":"Prenatal Screening and Diagnostics","field":"Medicine","cited_by":70,"is_retracted":false,"has_abstract":true,"route_ca_aff":false,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"","funders":"Eunice Kennedy Shriver National Institute of Child Health and Human Development; National Center for Research Resources; National Institute of Child Health and Human Development; Natural Sciences and Engineering Research Council of Canada; Yale University; National Institutes of Health; National Human Genome Research Institute","keywords":"Single-nucleotide polymorphism; Copy-number variation; SNP; Genetics; Genome-wide association study; SNP array; Biology; Candidate gene; Genetic association; Case-control study; Pregnancy; Medicine; Bioinformatics; Genotype; Genome; Internal medicine; Gene","score_opus":0.039725777298461544,"score_gpt":0.2979637918709384,"score_spread":0.25823801457247686,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1904831760","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9989378,0.0000663431,0.00020076054,0.000011465317,0.0000027822512,0.0000126252435,0.00050628546,0.0000038965313,0.00025813],"genre_scores_gemma":[0.99821234,0.00008422005,0.00033999726,0.000016899441,0.000006179363,0.00003156876,0.0010691343,0.0000054155907,0.00023423058],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99958366,0.00011102823,0.000039704828,0.00014627299,0.00006124327,0.000058104302],"domain_scores_gemma":[0.9994229,0.00013790546,0.00012732003,0.0001551942,0.000046339697,0.00011028524],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0006262849,0.0002464003,0.00034126887,0.00048405616,0.00047425285,0.0005655341,0.00028137257,0.00024843396,0.0011716378],"category_scores_gemma":[0.0016218455,0.00021927599,0.00032982367,0.00073269533,0.00018249724,0.00011125624,0.0005244861,0.00033558073,0.00012407418],"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":[0.0006353872,0.00003679872,0.9884791,0.000014065922,0.00024324129,0.00038380377,0.00022249515,0.00010311995,0.006748318,0.00006297299,0.00022961396,0.0028410654],"study_design_scores_gemma":[0.000020626927,0.000039512946,0.99893683,0.0000024537012,0.000061940504,0.00027608447,0.00005729336,0.00014646874,0.00022038636,0.000022409156,0.00021317213,0.000002880197],"about_ca_topic_score_codex":0.0076984297,"about_ca_topic_score_gemma":0.009526273,"teacher_disagreement_score":0.0076984297,"about_ca_system_score_codex":0.00014117449,"about_ca_system_score_gemma":0.00023188487,"threshold_uncertainty_score":0.015307188},"labels":[],"label_agreement":null},{"id":"W1907116883","doi":"10.1111/j.1469-1809.2011.00641.x","title":"Investigation of the HIN200 Locus in UK SLE Families Identifies Novel Copy Number Variants","year":2011,"lang":"en","type":"article","venue":"Annals of Human Genetics","topic":"Systemic Lupus Erythematosus Research","field":"Medicine","cited_by":6,"is_retracted":false,"has_abstract":true,"route_ca_aff":false,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"","funders":"National Center for Research Resources; National Institute of General Medical Sciences; National Human Genome Research Institute; Canadian Institutes of Health Research; Versus Arthritis; Broad Institute; Wellcome Trust","keywords":"Locus (genetics); Single-nucleotide polymorphism; Genetics; Biology; Copy-number variation; International HapMap Project; Genome-wide association study; Candidate gene; SNP; Genetic association; Disease; Gene; Genotype; Medicine; Genome; Internal medicine","score_opus":0.16329019204772574,"score_gpt":0.3574459141345321,"score_spread":0.19415572208680634,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1907116883","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9990019,0.00016265146,0.00027867136,0.000034853307,0.0000023398343,0.0000063464418,0.00014618004,0.000007604408,0.00035936205],"genre_scores_gemma":[0.9991068,0.00008789196,0.00035238048,0.000025310832,0.0000055300306,0.000008137958,0.00012717664,0.0000037134023,0.00028304823],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99955636,0.00013180634,0.000038385715,0.00012096984,0.00009007041,0.00006234165],"domain_scores_gemma":[0.99906474,0.0004624238,0.00025664206,0.00006857871,0.000065451924,0.00008215276],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0003347177,0.0003315115,0.0003430868,0.0010159599,0.00045318398,0.0004130918,0.00026974725,0.00046509178,0.003302694],"category_scores_gemma":[0.0026103908,0.00018622311,0.00024524413,0.0009661291,0.00028434902,0.00014460817,0.00036979263,0.0002520663,0.00028046785],"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":[0.0012638875,0.00007906936,0.9289394,0.00008106913,0.00015711822,0.006902717,0.0016550012,0.0004757566,0.03766268,0.0004510079,0.0005412987,0.021791],"study_design_scores_gemma":[0.00006866332,0.00028297957,0.98642933,0.000025692916,0.00006882544,0.007990275,0.00026861762,0.0005424802,0.0029044237,0.00013899225,0.0012657144,0.0000140569555],"about_ca_topic_score_codex":0.004890882,"about_ca_topic_score_gemma":0.006440748,"teacher_disagreement_score":0.004890882,"about_ca_system_score_codex":0.0002890911,"about_ca_system_score_gemma":0.0001680306,"threshold_uncertainty_score":0.011048615},"labels":[],"label_agreement":null},{"id":"W1915920625","doi":"10.1111/j.1469-1809.2011.00642.x","title":"A Molecular‐Based Estimation of the Prevalence of Hypophosphatasia in the European Population","year":2011,"lang":"en","type":"article","venue":"Annals of Human Genetics","topic":"Alkaline Phosphatase Research Studies","field":"Medicine","cited_by":232,"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":"Hypophosphatasia; Penetrance; Allele; Genetics; Population; Heterozygote advantage; Incidence (geometry); Genotype; Biology; Prevalence; Allele frequency; Medicine; Gene; Alkaline phosphatase; Enzyme; Phenotype; Environmental health","score_opus":0.12240254021076218,"score_gpt":0.3777455900194074,"score_spread":0.2553430498086452,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1915920625","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9927666,0.0015976168,0.0028455104,0.00009799612,0.000012334544,0.000030255524,0.00075942394,0.00003894286,0.00185133],"genre_scores_gemma":[0.9958352,0.0008437445,0.0022177044,0.000060529324,0.000020096792,0.00003324593,0.0007431582,0.000004820301,0.00024157135],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99890363,0.0005254547,0.00013699042,0.00020564068,0.00018178645,0.00004650527],"domain_scores_gemma":[0.9990989,0.00023292651,0.00032256654,0.00008474689,0.0001983815,0.00006249708],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0019428143,0.00037770075,0.00037077026,0.0028653352,0.00026272007,0.0006574929,0.00054092135,0.000763551,0.00131723],"category_scores_gemma":[0.0033121298,0.0002678189,0.00037375715,0.001317062,0.00030940466,0.00043696084,0.00039028414,0.00028929737,0.00045952093],"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":[0.00010808874,0.000022692591,0.98954076,0.000026968044,0.00013349393,0.000097742275,0.00008601903,0.0002493362,0.0017042282,0.00014282376,0.00017882825,0.007709038],"study_design_scores_gemma":[0.000008726877,0.00009593264,0.9962147,0.000015735532,0.00004327373,0.00129652,0.00009636287,0.001050363,0.00042635368,0.00008285699,0.000662582,0.0000067096785],"about_ca_topic_score_codex":0.004829552,"about_ca_topic_score_gemma":0.0019099896,"teacher_disagreement_score":0.004829552,"about_ca_system_score_codex":0.00031914213,"about_ca_system_score_gemma":0.00015257647,"threshold_uncertainty_score":0.010274708},"labels":[],"label_agreement":null},{"id":"W1943789301","doi":"10.1111/ahg.12000","title":"Initial Assessment of the Pathogenic Mechanisms of the Recently Identified Alzheimer Risk Loci","year":2013,"lang":"en","type":"article","venue":"Annals of Human Genetics","topic":"Genetic Associations and Epidemiology","field":"Biochemistry, Genetics and Molecular Biology","cited_by":48,"is_retracted":false,"has_abstract":true,"route_ca_aff":false,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"","funders":"National Center for Research Resources; National Institute of Neurological Disorders and Stroke; Canadian Institutes of Health Research; National Institutes of Health; National Cancer Institute; Medpace; National Human Genome Research Institute; Wellcome Trust; F. Hoffmann-La Roche; National Institute of Mental Health; Howard Hughes Medical Institute; Medical Research Council; Merck; National Institute on Aging; Eli Lilly and Company","keywords":"Expression quantitative trait loci; Genome-wide association study; Biology; Genetic association; Apolipoprotein E; Disease; Quantitative trait locus; Genetics; Alzheimer's disease; Gene; Single-nucleotide polymorphism; Genotype; Medicine; Pathology","score_opus":0.058594747687117164,"score_gpt":0.35449578908461393,"score_spread":0.2959010413974968,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1943789301","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.95257175,0.015648127,0.021388251,0.0024204622,0.00009514475,0.00013464552,0.0005041526,0.00006189699,0.0071754684],"genre_scores_gemma":[0.98464495,0.0044201687,0.008988381,0.00039143814,0.00011443743,0.000058436715,0.00028213006,0.000015206058,0.0010848269],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9984871,0.00076971034,0.00011900658,0.00025551394,0.00024838132,0.00012013801],"domain_scores_gemma":[0.9944265,0.0035376926,0.00055600563,0.00047016534,0.00079197896,0.00021770826],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0042090416,0.00083017955,0.0006912964,0.0014736047,0.00061884813,0.00095843244,0.0007535147,0.0008477794,0.0019761652],"category_scores_gemma":[0.007147051,0.0002002772,0.0006143276,0.0010759891,0.0009958014,0.0007653554,0.0011075669,0.001315961,0.00024751472],"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":[0.0043696812,0.0004026735,0.68322664,0.0012423893,0.00086188345,0.007284456,0.0020760074,0.002559838,0.17846759,0.00946055,0.0006370336,0.10941133],"study_design_scores_gemma":[0.00011798242,0.0017849823,0.90856177,0.00024137809,0.0012247586,0.013749134,0.001476436,0.004855649,0.03828751,0.020050691,0.009554987,0.00009464662],"about_ca_topic_score_codex":0.0013256599,"about_ca_topic_score_gemma":0.0016320484,"teacher_disagreement_score":0.0042090416,"about_ca_system_score_codex":0.00033435508,"about_ca_system_score_gemma":0.0004819636,"threshold_uncertainty_score":0.022259831},"labels":[],"label_agreement":null},{"id":"W1968659435","doi":"10.1111/j.1469-1809.2006.00277.x","title":"Quantitative‐trait‐locus Mapping in the Presence of Locus Heterogeneity","year":2006,"lang":"en","type":"article","venue":"Annals of Human Genetics","topic":"Genetic Mapping and Diversity in Plants and Animals","field":"Biochemistry, Genetics and Molecular Biology","cited_by":2,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Memorial University of Newfoundland","funders":"","keywords":"Locus (genetics); Quantitative trait locus; Genetics; Biology; Trait; Evolutionary biology; Gene; Computer science","score_opus":0.07396048132801686,"score_gpt":0.31925407082415286,"score_spread":0.245293589496136,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1968659435","genre_codex":"methods","genre_gemma":"methods","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"methods","genre_consensus":"methods","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.13982041,0.0003463609,0.85658765,0.0006412079,0.0000659183,0.00006677819,0.00022077748,0.0002288771,0.0020220738],"genre_scores_gemma":[0.94142276,0.00025835293,0.056759227,0.00020537237,0.00006129126,0.00013864037,0.00019649338,0.00005433778,0.0009034041],"study_design_codex":"theoretical_or_conceptual","study_design_gemma":"theoretical_or_conceptual","domain_scores_codex":[0.991546,0.005589909,0.0002589086,0.0012796624,0.0009752079,0.00035043413],"domain_scores_gemma":[0.8631232,0.1241467,0.00527611,0.006013526,0.00085522234,0.00058521976],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.025011238,0.00053099013,0.0019338782,0.00094619184,0.0007614782,0.0018410112,0.0022945134,0.001553221,0.0016099127],"category_scores_gemma":[0.072892666,0.000585365,0.0014632472,0.0019741764,0.0031160126,0.0024301682,0.0015856737,0.0018664536,0.00023718347],"study_design_candidate":"theoretical_or_conceptual","study_design_consensus":"theoretical_or_conceptual","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00076667423,0.00018346966,0.11910138,0.0004625507,0.0015542686,0.0046672216,0.001473209,0.3312758,0.020532984,0.43114352,0.0021017725,0.086737186],"study_design_scores_gemma":[0.0001697059,0.00030600376,0.020075783,0.00006154763,0.0002682649,0.0015785205,0.00021643702,0.4768715,0.0032033876,0.4946228,0.0024911321,0.00013493898],"about_ca_topic_score_codex":0.0020311892,"about_ca_topic_score_gemma":0.0011253405,"teacher_disagreement_score":0.025011238,"about_ca_system_score_codex":0.0007147504,"about_ca_system_score_gemma":0.00074337196,"threshold_uncertainty_score":0.13227367},"labels":[],"label_agreement":null},{"id":"W1969851802","doi":"10.1046/j.1529-8817.2004.00056.x","title":"Standardizing a Composite Measure of Linkage Disequilibrium","year":2004,"lang":"en","type":"article","venue":"Annals of Human Genetics","topic":"Genetic Mapping and Diversity in Plants and Animals","field":"Biochemistry, Genetics and Molecular Biology","cited_by":24,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Toronto; Dalhousie University","funders":"Natural Sciences and Engineering Research Council of Canada","keywords":"Linkage disequilibrium; Disequilibrium; Measure (data warehouse); Linkage (software); Genetics; Biology; Evolutionary biology; Statistics; Mathematics; Haplotype; Genotype; Gene; Computer science; Data mining; Medicine","score_opus":0.04708241112833955,"score_gpt":0.2996577492976195,"score_spread":0.25257533816927996,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1969851802","genre_codex":"methods","genre_gemma":"methods","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"methods","genre_consensus":"methods","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.042485278,0.00024722313,0.9518467,0.00011168966,0.00010246454,0.00009181096,0.00026893872,0.00049000897,0.004355835],"genre_scores_gemma":[0.2602417,0.00028755903,0.73563015,0.00014166663,0.00011810957,0.00041023534,0.0010080193,0.00046709905,0.0016954525],"study_design_codex":"design_other","study_design_gemma":"theoretical_or_conceptual","domain_scores_codex":[0.98437274,0.00509588,0.00115481,0.004084481,0.0048217797,0.00047030492],"domain_scores_gemma":[0.9629712,0.017837124,0.0029987092,0.0067940536,0.008658091,0.000740784],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.019929882,0.00081295084,0.0015175866,0.0061018113,0.0010678469,0.0052635456,0.002047586,0.0012655322,0.0026475906],"category_scores_gemma":[0.079278685,0.0006017898,0.001039175,0.004970891,0.002548789,0.003948016,0.0039564986,0.002103561,0.0010089211],"study_design_candidate":"theoretical_or_conceptual","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0006084984,0.00022999481,0.04407137,0.00075462,0.0007148337,0.00025294942,0.0022408229,0.04224733,0.042847075,0.27084622,0.0047967867,0.59038955],"study_design_scores_gemma":[0.00018418158,0.00094904494,0.0645291,0.00037321623,0.0004226663,0.0015224667,0.001142106,0.24978098,0.06294059,0.5755923,0.04181897,0.00074442953],"about_ca_topic_score_codex":0.00072727096,"about_ca_topic_score_gemma":0.00076485885,"teacher_disagreement_score":0.019929882,"about_ca_system_score_codex":0.0012035324,"about_ca_system_score_gemma":0.0017458918,"threshold_uncertainty_score":0.10540056},"labels":[],"label_agreement":null},{"id":"W1976246921","doi":"10.1111/j.1469-1809.2006.00267.x","title":"The Merits of Testing Hardy‐Weinberg Equilibrium in the Analysis of Unmatched Case‐Control Data: A Cautionary Note","year":2006,"lang":"en","type":"article","venue":"Annals of Human Genetics","topic":"Genetic Associations and Epidemiology","field":"Biochemistry, Genetics and Molecular Biology","cited_by":104,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Robarts Clinical Trials; Western University","funders":"Natural Sciences and Engineering Research Council of Canada","keywords":"Genotyping; Statistic; Hardy–Weinberg principle; Statistics; Context (archaeology); Test (biology); Test statistic; Chi-square test; Statistical hypothesis testing; Econometrics; Mathematics; Computer science; Allele frequency; Genetics; Biology; Allele; Genotype","score_opus":0.07702611504157066,"score_gpt":0.3585877522888192,"score_spread":0.28156163724724853,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1976246921","genre_codex":"methods","genre_gemma":"methods","domain_codex":null,"domain_gemma":"methods","model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"methods","genre_consensus":"methods","domain_candidate":"methods","domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.034374405,0.029811915,0.4652006,0.409832,0.04787582,0.0011683195,0.00093154993,0.0017520189,0.009053387],"genre_scores_gemma":[0.2553849,0.009514809,0.40767327,0.27274486,0.044318214,0.0021183568,0.00026482544,0.0011300419,0.0068506724],"study_design_codex":"design_other","study_design_gemma":"theoretical_or_conceptual","domain_scores_codex":[0.64858395,0.26940426,0.030269967,0.015083191,0.035532348,0.0011262477],"domain_scores_gemma":[0.2653051,0.6770026,0.010444641,0.027592292,0.017525239,0.0021300768],"candidate_categories":["metaresearch"],"consensus_categories":["metaresearch"],"category_scores_codex":[0.36786544,0.0016349381,0.0051510613,0.0040342403,0.0030914298,0.0069681136,0.009654347,0.008201935,0.0019486822],"category_scores_gemma":[0.60670257,0.0010734132,0.002836116,0.0045834333,0.019923344,0.006960746,0.0034552487,0.024772504,0.0014568426],"study_design_candidate":"theoretical_or_conceptual","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.003315311,0.0003990843,0.06299364,0.0063243415,0.004072481,0.012886039,0.022555659,0.0032483358,0.0049739014,0.13695832,0.270547,0.47172594],"study_design_scores_gemma":[0.0012903037,0.0022398317,0.067974664,0.00964917,0.0019532817,0.01949643,0.009331881,0.036296975,0.011086259,0.6100541,0.22917597,0.0014512088],"about_ca_topic_score_codex":0.0042900937,"about_ca_topic_score_gemma":0.0060973857,"teacher_disagreement_score":0.63213456,"about_ca_system_score_codex":0.0017440089,"about_ca_system_score_gemma":0.0027555998,"threshold_uncertainty_score":0.77953446},"labels":[],"label_agreement":null},{"id":"W1987735559","doi":"10.1111/j.1469-1809.2009.00546.x","title":"A Mutation that Creates a Pseudoexon in <i>SOD1</i> Causes Familial ALS","year":2009,"lang":"en","type":"article","venue":"Annals of Human Genetics","topic":"Amyotrophic Lateral Sclerosis Research","field":"Medicine","cited_by":35,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Université de Montréal","funders":"","keywords":"Exon; Amyotrophic lateral sclerosis; Genetics; SOD1; Biology; Intron; Gene; Locus (genetics); Mutation; Medicine; Disease; Pathology","score_opus":0.1370918794286901,"score_gpt":0.39648497523155257,"score_spread":0.25939309580286246,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1987735559","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9971896,0.00015686272,0.0010310428,0.00010615248,0.00003877366,0.000027718479,0.00009484417,0.00007200544,0.0012831736],"genre_scores_gemma":[0.99780995,0.00014628982,0.0009335479,0.00010970424,0.000042079628,0.000012378044,0.00017746587,0.000024964402,0.0007436994],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9998596,0.000039994775,0.000017183404,0.00002811886,0.00003268066,0.000022419013],"domain_scores_gemma":[0.99967563,0.00012033299,0.00010223002,0.000020946702,0.000017681234,0.00006322275],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0002273282,0.000768014,0.00022966605,0.0004099063,0.00031498825,0.00020209476,0.00028776654,0.0006141031,0.0021863147],"category_scores_gemma":[0.0003395699,0.00018604881,0.0003173581,0.00016981605,0.00046632477,0.00012175613,0.0003136538,0.0004953088,0.0007012449],"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":[0.0009901199,0.0005554143,0.028115641,0.00017683304,0.00014376231,0.07854919,0.00043873244,0.00070836296,0.87058175,0.0013435921,0.002181718,0.01621492],"study_design_scores_gemma":[0.0006621245,0.002863272,0.22073445,0.00015831177,0.00042205965,0.39225262,0.00047641943,0.006410004,0.3423793,0.001741418,0.031787083,0.000112860456],"about_ca_topic_score_codex":0.00032483635,"about_ca_topic_score_gemma":0.0004051481,"teacher_disagreement_score":0.0021863147,"about_ca_system_score_codex":0.00017749939,"about_ca_system_score_gemma":0.00011632361,"threshold_uncertainty_score":0.0073139668},"labels":[],"label_agreement":null},{"id":"W1988853199","doi":"10.1111/j.1469-1809.2007.00389.x","title":"The Birth Prevalence of PKU in Populations of European, South Asian and Sub‐Saharan African Ancestry Living in South East England","year":2007,"lang":"en","type":"article","venue":"Annals of Human Genetics","topic":"Metabolism and Genetic Disorders","field":"Biochemistry, Genetics and Molecular Biology","cited_by":56,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"McGill University Health Centre; Montreal Children's Hospital","funders":"Medical Research Council; Great Ormond Street Hospital for Children","keywords":"Demography; Ethnic group; Population; Phenylalanine hydroxylase; Newborn screening; Medicine; Mongoloid; Pediatrics; Geography; Biology; Genetics; Environmental health","score_opus":0.04831622558819513,"score_gpt":0.2996373067324733,"score_spread":0.25132108114427815,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1988853199","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9990933,0.00029524168,0.000075676595,0.000021939106,0.0000014894977,0.0000058400506,0.00024285176,0.0000017332559,0.0002618834],"genre_scores_gemma":[0.9990533,0.0003605828,0.00012488653,0.000014038952,0.000002195766,0.000012160018,0.00020614611,0.0000011155355,0.0002255241],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9994874,0.00017043408,0.00009310871,0.00013207985,0.00006305118,0.000053999283],"domain_scores_gemma":[0.9991104,0.00021542596,0.00039001124,0.00007557836,0.000113462396,0.00009503747],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00064103137,0.00018142968,0.0003098829,0.0007969999,0.0003179486,0.00054414093,0.00034599195,0.00028410647,0.0015510367],"category_scores_gemma":[0.0021491682,0.0003650128,0.00031313006,0.0007455776,0.00043023218,0.0004606465,0.00067310006,0.00032016303,0.00028762306],"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":[0.0000535711,0.0000070365827,0.9963832,0.000030889,0.0000528722,0.000182675,0.0011678251,0.0000697597,0.00036328778,0.000052545518,0.00008364134,0.0015526206],"study_design_scores_gemma":[0.0000027627716,0.00002112264,0.9990128,0.000012228531,0.000015826028,0.0002342651,0.00045826175,0.00008352255,0.000034804496,0.000013988588,0.000107522086,0.0000028619554],"about_ca_topic_score_codex":0.058429454,"about_ca_topic_score_gemma":0.05559186,"teacher_disagreement_score":0.058429454,"about_ca_system_score_codex":0.0006312567,"about_ca_system_score_gemma":0.00028038307,"threshold_uncertainty_score":0.11617869},"labels":[],"label_agreement":null},{"id":"W1992657963","doi":"10.1111/j.1529-8817.2005.00213.x","title":"Statistical Methods for the Analysis of Genetic Association Studies","year":2005,"lang":"en","type":"article","venue":"Annals of Human Genetics","topic":"Genetic Associations and Epidemiology","field":"Biochemistry, Genetics and Molecular Biology","cited_by":47,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Robarts Clinical Trials; Western University","funders":"Natural Sciences and Engineering Research Council of Canada","keywords":"Genetic association; Association (psychology); Genetics; Biology; Evolutionary biology; Statistical analysis; Computational biology; Statistics; Mathematics; Genotype; Psychology; Single-nucleotide polymorphism; Gene","score_opus":0.1196123382124523,"score_gpt":0.4852117100838845,"score_spread":0.36559937187143215,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1992657963","genre_codex":"methods","genre_gemma":"methods","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"methods","genre_consensus":"methods","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.0004952863,0.0014870457,0.9877071,0.000511544,0.0006569211,0.0014473761,0.0024672078,0.0034871418,0.0017403911],"genre_scores_gemma":[0.004793416,0.0013065578,0.9766718,0.0003211319,0.00045403143,0.01259359,0.0015439373,0.0012244232,0.0010910127],"study_design_codex":"design_other","study_design_gemma":"theoretical_or_conceptual","domain_scores_codex":[0.9420547,0.03972451,0.006242719,0.0028734356,0.008589186,0.0005153946],"domain_scores_gemma":[0.74162847,0.21597329,0.010432725,0.021676078,0.008911766,0.0013776524],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.052275587,0.0030092387,0.0049305726,0.009129903,0.0014066865,0.003214285,0.0046542836,0.0023219427,0.03388252],"category_scores_gemma":[0.21721026,0.0017792695,0.0029406687,0.011186841,0.0030558957,0.002475312,0.0037404066,0.011140872,0.014086396],"study_design_candidate":"theoretical_or_conceptual","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0006780108,0.00054746936,0.0041758744,0.007534071,0.002490129,0.0009356312,0.0012339277,0.018061247,0.0033583723,0.22994289,0.1751724,0.55587],"study_design_scores_gemma":[0.0007864103,0.0008838425,0.006408408,0.003069662,0.0007397687,0.0016134114,0.0004145411,0.05434591,0.0017814856,0.54616654,0.38351855,0.00027150774],"about_ca_topic_score_codex":0.0016013599,"about_ca_topic_score_gemma":0.0015523547,"teacher_disagreement_score":0.052275587,"about_ca_system_score_codex":0.0015945642,"about_ca_system_score_gemma":0.0055132126,"threshold_uncertainty_score":0.27646303},"labels":[],"label_agreement":null},{"id":"W1994711454","doi":"10.1111/j.1469-1809.2006.00254.x","title":"Approximate Variance for a Standardized Composite Measure of Linkage Disequilibrium","year":2006,"lang":"en","type":"article","venue":"Annals of Human Genetics","topic":"Evolution and Genetic Dynamics","field":"Biochemistry, Genetics and Molecular Biology","cited_by":3,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Toronto; Dalhousie University","funders":"Natural Sciences and Engineering Research Council of Canada","keywords":"Disequilibrium; Linkage disequilibrium; Measure (data warehouse); Variance (accounting); Linkage (software); Mathematics; Statistics; Hardy–Weinberg principle; Econometrics; Statistical physics; Allele frequency; Genetics; Biology; Allele; Physics; Economics; Computer science; Haplotype","score_opus":0.02469307817746976,"score_gpt":0.30569634956983555,"score_spread":0.2810032713923658,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1994711454","genre_codex":"methods","genre_gemma":"methods","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"methods","genre_consensus":"methods","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.009150511,0.00027141997,0.9880861,0.00012718103,0.00005566423,0.000029374502,0.00008460272,0.00018568143,0.0020095012],"genre_scores_gemma":[0.3549309,0.0008518331,0.635857,0.0003148922,0.00020097097,0.00042083501,0.0005924388,0.00050619204,0.006324915],"study_design_codex":"theoretical_or_conceptual","study_design_gemma":"theoretical_or_conceptual","domain_scores_codex":[0.99512154,0.0019044332,0.0002255732,0.00087119656,0.0015907825,0.00028636502],"domain_scores_gemma":[0.98350483,0.011119095,0.00084544846,0.0024734514,0.0018295522,0.00022762665],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0061018835,0.00060675136,0.0010482275,0.0015653416,0.00057506096,0.002288698,0.002057163,0.0013239445,0.0045044953],"category_scores_gemma":[0.034923155,0.00042461674,0.00104054,0.0018414863,0.0018206189,0.0038365782,0.0017666027,0.0019147323,0.0012265547],"study_design_candidate":"theoretical_or_conceptual","study_design_consensus":"theoretical_or_conceptual","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00008278412,0.000036431076,0.003654079,0.00016866038,0.00011759087,0.00018445027,0.00020515274,0.25140545,0.004015307,0.68432826,0.002968505,0.05283332],"study_design_scores_gemma":[0.000022363529,0.0000639931,0.0019448708,0.000057419424,0.00003435767,0.0005053399,0.000044792127,0.65599823,0.0016887463,0.33439398,0.0051668664,0.00007911602],"about_ca_topic_score_codex":0.0012218974,"about_ca_topic_score_gemma":0.0010980337,"teacher_disagreement_score":0.0061018835,"about_ca_system_score_codex":0.001275334,"about_ca_system_score_gemma":0.00117832,"threshold_uncertainty_score":0.032270193},"labels":[],"label_agreement":null},{"id":"W2028418054","doi":"10.1046/j.1529-8817.2004.00081.x","title":"Age Related Changes in 5‐methylcytosine Content in Human Peripheral Leukocytes and Placentas: an HPLC‐based Study","year":2004,"lang":"en","type":"article","venue":"Annals of Human Genetics","topic":"Epigenetics and DNA Methylation","field":"Biochemistry, Genetics and Molecular Biology","cited_by":396,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Centre for Addiction and Mental Health","funders":"","keywords":"Epigenetics; DNA methylation; Methylation; Biology; Andrology; Gestational age; Peripheral blood; Physiology; Gene expression; DNA; Endocrinology; Gene; Genetics; Pregnancy; Immunology; Medicine","score_opus":0.09116712813891109,"score_gpt":0.3532036683112965,"score_spread":0.2620365401723854,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2028418054","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99685466,0.0017881849,0.00085798575,0.000013022124,0.0000039159886,0.0000069633847,0.0002019544,0.0000074012523,0.00026592216],"genre_scores_gemma":[0.9969541,0.0010430907,0.001089294,0.000027247508,0.000010211601,0.000014286515,0.00033071946,0.0000047084973,0.00052637805],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.99991727,0.00002090237,0.000005927915,0.000027298123,0.000017263372,0.000011237391],"domain_scores_gemma":[0.99984205,0.00003579641,0.00005513227,0.0000150365595,0.000033770048,0.000018119885],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00017398852,0.00012831604,0.00015005801,0.00037718422,0.00011173382,0.00021361384,0.000081886836,0.00018694345,0.0006231456],"category_scores_gemma":[0.00041411695,0.00010354253,0.00007319611,0.00039955406,0.00010590406,0.00010856493,0.000099315585,0.0001466417,0.00017425782],"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":[0.001481765,0.00007968466,0.2907582,0.00013343473,0.00009729948,0.00034582228,0.0006433299,0.00014927813,0.6865201,0.0000681566,0.00009467101,0.019628273],"study_design_scores_gemma":[0.000013117996,0.0008564975,0.91400003,0.000010162423,0.00009549777,0.0019813487,0.00020158908,0.00043083786,0.08082505,0.00006517812,0.0015110662,0.000009636079],"about_ca_topic_score_codex":0.00114356,"about_ca_topic_score_gemma":0.0008659835,"teacher_disagreement_score":0.00114356,"about_ca_system_score_codex":0.000090137764,"about_ca_system_score_gemma":0.00008817932,"threshold_uncertainty_score":0.0022738576},"labels":[],"label_agreement":null},{"id":"W2029601543","doi":"10.1111/j.1469-1809.2008.00442.x","title":"The Power and Robustness of Maximum LOD Score Statistics","year":2008,"lang":"en","type":"article","venue":"Annals of Human Genetics","topic":"Genetic Associations and Epidemiology","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":"Mount Sinai Hospital","funders":"National Institute of Mental Health","keywords":"Phenocopy; Statistics; Mathematics; Statistic; Genetic model; Range (aeronautics); Biology; Genetics; Gene","score_opus":0.05229972903484332,"score_gpt":0.31515567584143805,"score_spread":0.26285594680659474,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2029601543","genre_codex":"methods","genre_gemma":"empirical","domain_codex":null,"domain_gemma":"methods","model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":null,"domain_candidate":"methods","domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.3367133,0.0010337954,0.6511411,0.0010652617,0.0001407511,0.00033429152,0.000902332,0.0010753283,0.0075937207],"genre_scores_gemma":[0.9420506,0.00024390552,0.055637404,0.00019011619,0.00012732552,0.00028091486,0.0007209531,0.00034701556,0.00040185274],"study_design_codex":"simulation_or_modeling","study_design_gemma":"simulation_or_modeling","domain_scores_codex":[0.88510686,0.086546354,0.004789414,0.010350719,0.011720393,0.0014862637],"domain_scores_gemma":[0.28181347,0.6692207,0.009997509,0.03274027,0.0054329243,0.00079517363],"candidate_categories":["metaresearch"],"consensus_categories":[],"category_scores_codex":[0.1424433,0.001282529,0.0023449555,0.0050440426,0.001022908,0.0036481267,0.0028484587,0.0023256782,0.00310027],"category_scores_gemma":[0.5229817,0.0008663099,0.0029191915,0.0026058287,0.0072646583,0.0067335344,0.004148014,0.0025080328,0.00058004167],"study_design_candidate":"simulation_or_modeling","study_design_consensus":"simulation_or_modeling","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.004764981,0.00032107125,0.169146,0.0009885636,0.0045134285,0.0014693288,0.0025431437,0.39586997,0.007325581,0.1609108,0.004253012,0.24789417],"study_design_scores_gemma":[0.00077955006,0.0016020504,0.061402883,0.0003758329,0.000822654,0.0026150474,0.00066006166,0.57968366,0.012987042,0.3332709,0.0054172277,0.0003831162],"about_ca_topic_score_codex":0.0009834657,"about_ca_topic_score_gemma":0.00034971687,"teacher_disagreement_score":0.8575567,"about_ca_system_score_codex":0.001089905,"about_ca_system_score_gemma":0.0009534041,"threshold_uncertainty_score":0.7533212},"labels":[],"label_agreement":null},{"id":"W2034525997","doi":"10.1111/j.1469-1809.2005.00242.x","title":"Effect of Environmental Factors and Gender on the Heritability of Bone Mineral Density and Bone Size","year":2006,"lang":"en","type":"article","venue":"Annals of Human Genetics","topic":"Bone health and osteoporosis research","field":"Medicine","cited_by":86,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"SickKids Foundation; Hospital for Sick Children; University of Toronto","funders":"Queen Mary University of London","keywords":"Heritability; Bone mineral; Osteoporosis; Analysis of variance; Bone density; Internal medicine; Medicine; Biology; Endocrinology; Demography; Genetics","score_opus":0.04859879672128911,"score_gpt":0.3414970819030854,"score_spread":0.2928982851817963,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2034525997","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9979067,0.00046215087,0.00092702155,0.00005529151,0.000008037823,0.0000045824827,0.000104586376,0.000010314403,0.00052122865],"genre_scores_gemma":[0.9993629,0.000093637325,0.0002637134,0.000011494539,0.0000052598134,0.0000024234666,0.000069719004,0.0000040852983,0.00018677909],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99873513,0.00067823456,0.00004636052,0.00024649105,0.00015989109,0.00013389438],"domain_scores_gemma":[0.9980281,0.0012217492,0.00030766762,0.0002538482,0.00008168973,0.00010682838],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.002142239,0.00040089988,0.00034379505,0.0005240731,0.00022297988,0.00035097473,0.0001658007,0.00017942204,0.0013879786],"category_scores_gemma":[0.0034138074,0.0002174482,0.00045626436,0.00027399216,0.0005957465,0.00019469857,0.00034366167,0.00021922145,0.00011214862],"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":[0.0002848078,0.00002150085,0.98378444,0.000010150297,0.0003132847,0.00047989984,0.0004587646,0.0003907594,0.004191647,0.00047188826,0.00010136895,0.009491501],"study_design_scores_gemma":[0.00000598263,0.000056213965,0.99775296,0.0000060247808,0.00008172004,0.00032856286,0.00008112647,0.00077198877,0.00035824426,0.00036017873,0.00019087327,0.0000060831044],"about_ca_topic_score_codex":0.0061256224,"about_ca_topic_score_gemma":0.006281616,"teacher_disagreement_score":0.0061256224,"about_ca_system_score_codex":0.00018911852,"about_ca_system_score_gemma":0.00027215772,"threshold_uncertainty_score":0.012179971},"labels":[],"label_agreement":null},{"id":"W2047079220","doi":"10.1046/j.1469-1809.2000.6440329.x","title":"Genetic diversity at the <i>FMR1</i> locus in the Indonesian population","year":2000,"lang":"en","type":"article","venue":"Annals of Human Genetics","topic":"Genetics and Neurodevelopmental Disorders","field":"Biochemistry, Genetics and Molecular Biology","cited_by":21,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Queen's University","funders":"","keywords":"Indonesian; Locus (genetics); Genetics; Allele; Allele frequency; Biology; Genetic diversity; Population; Evolutionary biology; Demography; Gene; Sociology","score_opus":0.027444243538938158,"score_gpt":0.26820079507466893,"score_spread":0.24075655153573078,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2047079220","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99956995,0.000040768988,0.000058949427,0.0000075464104,0.0000011191116,0.0000028472239,0.00004762484,0.0000013205309,0.00027001742],"genre_scores_gemma":[0.9994709,0.000057253837,0.00013533082,0.000009564957,0.000003624152,0.0000041398434,0.00010046598,0.0000011891339,0.00021753137],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99985707,0.00002855574,0.00001530035,0.00004830277,0.00003194668,0.000018902183],"domain_scores_gemma":[0.99985826,0.000025175521,0.000039464507,0.0000181644,0.000024246829,0.00003472145],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00021775714,0.00018880807,0.00023863108,0.0004644988,0.00040415808,0.0002966201,0.00013742302,0.00012558002,0.0009402587],"category_scores_gemma":[0.00039793493,0.00011194305,0.00011355216,0.00027904834,0.00034576622,0.00012354174,0.00021355906,0.00018393814,0.00020973227],"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":[0.00032939666,0.000076192926,0.9669213,0.000018550567,0.00006377381,0.0005312154,0.0015185098,0.00008742905,0.013693348,0.0001117839,0.000121726574,0.016526744],"study_design_scores_gemma":[0.0000057259304,0.00015939202,0.9970325,0.0000037507511,0.000022542721,0.0013607745,0.00033911917,0.00011723435,0.00053847727,0.00004729871,0.0003670146,0.0000061404376],"about_ca_topic_score_codex":0.0025400864,"about_ca_topic_score_gemma":0.0028288376,"teacher_disagreement_score":0.0025400864,"about_ca_system_score_codex":0.00012704522,"about_ca_system_score_gemma":0.0000915701,"threshold_uncertainty_score":0.005050659},"labels":[],"label_agreement":null},{"id":"W2080554198","doi":"10.1111/j.1469-1809.2006.00289.x","title":"Epistasis Between Type 2 Diabetes Susceptibility Loci on Chromosomes 1q21‐25 and 10q23‐26 in Northern Europeans","year":2006,"lang":"en","type":"article","venue":"Annals of Human Genetics","topic":"Genetic Associations and Epidemiology","field":"Biochemistry, Genetics and Molecular Biology","cited_by":24,"is_retracted":false,"has_abstract":true,"route_ca_aff":false,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"","funders":"Diabetes UK; Natural Sciences and Engineering Research Council of Canada; Wellcome Trust","keywords":"Epistasis; Pedigree chart; Genetics; Locus (genetics); Genetic linkage; Biology; Linkage (software); Population; Evolutionary biology; Gene; Demography","score_opus":0.03764835752029095,"score_gpt":0.30559069125101157,"score_spread":0.2679423337307206,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2080554198","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99866533,0.00047120813,0.00027139724,0.000049058395,0.0000021495675,0.0000020304935,0.0000691045,0.000006837829,0.0004628616],"genre_scores_gemma":[0.99857557,0.00033260966,0.00042351655,0.00003089294,0.000005054189,0.0000054628126,0.00013374601,0.0000053150466,0.00048798596],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9987664,0.0004946994,0.00006112197,0.0003930474,0.00014816121,0.00013668556],"domain_scores_gemma":[0.9990426,0.0003925731,0.00027347918,0.000060990667,0.000104112485,0.00012633632],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0009814613,0.0004175404,0.00061941193,0.0015372363,0.0007542957,0.0008433963,0.00034299708,0.00045934287,0.0016718484],"category_scores_gemma":[0.0028018327,0.00023365278,0.00047287045,0.0013404647,0.00056401984,0.00014325413,0.00043178952,0.00025814396,0.00013923149],"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":[0.001389387,0.000050580504,0.9180592,0.00009282875,0.00062769785,0.0033971458,0.0032426985,0.0017763592,0.03687552,0.0009830042,0.00037386498,0.03313171],"study_design_scores_gemma":[0.000016805563,0.00003557019,0.9975661,0.000011784689,0.00008010769,0.00087033643,0.00021629757,0.0002476274,0.00024720858,0.00012793056,0.0005698258,0.000010344528],"about_ca_topic_score_codex":0.1032792,"about_ca_topic_score_gemma":0.13246746,"teacher_disagreement_score":0.1032792,"about_ca_system_score_codex":0.00094242924,"about_ca_system_score_gemma":0.00050438184,"threshold_uncertainty_score":0.20535612},"labels":[],"label_agreement":null},{"id":"W2080815950","doi":"10.1046/j.1469-1809.2001.6520127.x","title":"Distribution of <i>FMR1</i> and <i>FMR2</i> alleles in Javanese individuals with developmental disability and confirmation of a specific AGG‐interruption pattern in Asian populations","year":2001,"lang":"en","type":"article","venue":"Annals of Human Genetics","topic":"Genetics and Neurodevelopmental Disorders","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":"Queen's University","funders":"","keywords":"FMR1; Genetics; Trinucleotide repeat expansion; Biology; Allele; Fragile X syndrome; Population; Gene; Demography","score_opus":0.054511695950752934,"score_gpt":0.30512765204160874,"score_spread":0.2506159560908558,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2080815950","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99977666,0.000025142106,0.000035232482,0.0000055477626,5.661864e-7,0.0000010090716,0.000028143864,0.0000014465165,0.00012619341],"genre_scores_gemma":[0.9996793,0.000029582434,0.00010398746,0.000008808312,0.0000021789795,0.0000022828583,0.00005259079,0.0000020128678,0.000119259625],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99979323,0.000031680782,0.000027492499,0.000079382655,0.000032722306,0.000035465335],"domain_scores_gemma":[0.9997193,0.000051530522,0.0001291175,0.00002117228,0.000029524484,0.000049286824],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0001773801,0.00020950961,0.000202329,0.0009901079,0.0002706151,0.00025926722,0.00015480572,0.00021109873,0.0013291003],"category_scores_gemma":[0.00052009744,0.00018140046,0.00014284383,0.0003025416,0.00041204778,0.000100409445,0.00020478497,0.00018165229,0.0001795384],"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":[0.00050792104,0.00007695813,0.7752721,0.000032539512,0.00007923667,0.001917877,0.0015307456,0.00007316267,0.21132517,0.00013937271,0.00009931494,0.008945671],"study_design_scores_gemma":[0.00001107631,0.00011877102,0.99340516,0.000004140652,0.0000267092,0.0032607878,0.00026293268,0.00007191621,0.0026220817,0.000029781379,0.00018043873,0.0000061317783],"about_ca_topic_score_codex":0.0025973853,"about_ca_topic_score_gemma":0.0030997307,"teacher_disagreement_score":0.0025973853,"about_ca_system_score_codex":0.00016885389,"about_ca_system_score_gemma":0.00007424611,"threshold_uncertainty_score":0.0051645637},"labels":[],"label_agreement":null},{"id":"W2080822287","doi":"10.1111/j.1469-1809.2008.00492.x","title":"Heterogeneous Disease Modeling for Hardy‐Weinberg Disequilibrium in Case‐Control Studies: Application to Renal Stones and Calcium‐Sensing Receptor Polymorphisms","year":2008,"lang":"en","type":"article","venue":"Annals of Human Genetics","topic":"Kidney Stones and Urolithiasis Treatments","field":"Medicine","cited_by":29,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Toronto; Dalhousie University","funders":"","keywords":"Linkage disequilibrium; Single-nucleotide polymorphism; Biology; Genetics; Disequilibrium; Genetic association; Hypercalciuria; Population; Locus (genetics); SNP; Genotype; Genetic heterogeneity; Endocrinology; Phenotype; Gene; Medicine","score_opus":0.12620837105549867,"score_gpt":0.3817885476580864,"score_spread":0.2555801766025877,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2080822287","genre_codex":"methods","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":null,"domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.053333163,0.002109963,0.93734795,0.0015053937,0.0007494918,0.001909841,0.0009352927,0.00081830914,0.0012905949],"genre_scores_gemma":[0.5461047,0.0011664946,0.43581346,0.0011943543,0.0007532454,0.0076421066,0.0015500213,0.0003184797,0.0054570585],"study_design_codex":"simulation_or_modeling","study_design_gemma":"simulation_or_modeling","domain_scores_codex":[0.7371978,0.22152896,0.0068141585,0.0258069,0.0067310245,0.0019210529],"domain_scores_gemma":[0.6045579,0.3542079,0.010603542,0.02453447,0.004544086,0.0015521132],"candidate_categories":["metaresearch"],"consensus_categories":[],"category_scores_codex":[0.20633498,0.0043283915,0.006685219,0.0057623144,0.0026236137,0.003892012,0.010236806,0.006693425,0.0076386193],"category_scores_gemma":[0.3205195,0.0027667761,0.008063334,0.0060524223,0.0050562406,0.004305212,0.004597024,0.0071246056,0.0009531762],"study_design_candidate":"simulation_or_modeling","study_design_consensus":"simulation_or_modeling","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.007622762,0.001286274,0.25105122,0.002694199,0.036753744,0.009350548,0.0068440055,0.34486228,0.0022128762,0.15548456,0.008517223,0.17332035],"study_design_scores_gemma":[0.0011127446,0.0013234562,0.017887348,0.0003091501,0.0034956227,0.0014455201,0.0004929752,0.8805966,0.00045581732,0.08623967,0.006456587,0.0001844969],"about_ca_topic_score_codex":0.01229551,"about_ca_topic_score_gemma":0.0070711905,"teacher_disagreement_score":0.20633498,"about_ca_system_score_codex":0.0018104333,"about_ca_system_score_gemma":0.0027179243,"threshold_uncertainty_score":0.97873026},"labels":[],"label_agreement":null},{"id":"W2083171324","doi":"10.1111/j.1469-1809.2007.00375.x","title":"Persistence of the Common Hartnup Disease D173N Allele in Populations of European Origin","year":2007,"lang":"en","type":"article","venue":"Annals of Human Genetics","topic":"Amino Acid Enzymes and Metabolism","field":"Biochemistry, Genetics and Molecular Biology","cited_by":18,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Université de Sherbrooke","funders":"National Medical Research Council; National Institute of General Medical Sciences; National Health and Medical Research Council","keywords":"Genetics; Allele; Biology; Locus (genetics); Haplotype; Allele frequency; Gene","score_opus":0.09120286933061324,"score_gpt":0.34322261313301167,"score_spread":0.25201974380239844,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2083171324","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9994375,0.00011637431,0.00013888892,0.000019892368,0.0000032697208,0.0000018809869,0.000040277806,0.0000029131572,0.00023894633],"genre_scores_gemma":[0.9994412,0.000102070175,0.00012983629,0.000022542767,0.0000064546703,0.0000017188726,0.00006818053,0.000003767375,0.0002242072],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99969256,0.000050800412,0.00002995541,0.0001332888,0.000042906442,0.000050576164],"domain_scores_gemma":[0.9994479,0.000095060415,0.00020795285,0.000049341674,0.00007348642,0.00012634155],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00033107025,0.00027606392,0.00035073355,0.00071424956,0.0006722138,0.00041806733,0.00022400785,0.0004913866,0.0020925316],"category_scores_gemma":[0.0012285344,0.00017517741,0.00022153696,0.0006740691,0.0005121522,0.00031759718,0.0003867414,0.0003583591,0.0002490558],"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":[0.00052985485,0.000056788205,0.96104366,0.000023931163,0.00008394866,0.0039454955,0.0007126954,0.000045935714,0.021350643,0.00014836548,0.00016337987,0.011895319],"study_design_scores_gemma":[0.000019748662,0.00025533777,0.9779138,0.000014413884,0.000062056606,0.018261667,0.00057175773,0.00014873665,0.0018420703,0.00019626445,0.00069783337,0.000016294738],"about_ca_topic_score_codex":0.0028176794,"about_ca_topic_score_gemma":0.0037006103,"teacher_disagreement_score":0.0028176794,"about_ca_system_score_codex":0.00017651323,"about_ca_system_score_gemma":0.00018231428,"threshold_uncertainty_score":0.0070002675},"labels":[],"label_agreement":null},{"id":"W2084662104","doi":"10.1046/j.1529-8817.2003.00084.x","title":"Admixture in the Hispanics of the San Luis Valley, Colorado, and its implications for complex trait gene mapping","year":2004,"lang":"en","type":"article","venue":"Annals of Human Genetics","topic":"Genetic Associations and Epidemiology","field":"Biochemistry, Genetics and Molecular Biology","cited_by":164,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Toronto","funders":"National Institute of Diabetes and Digestive and Kidney Diseases; National Human Genome Research Institute; National Institute of Mental Health; National Institutes of Health","keywords":"Ancestry-informative marker; Genetic admixture; Biology; Population; Trait; Allele; Evolutionary biology; Genetic genealogy; Allele frequency; Genetic marker; Genetics; Demography; Gene","score_opus":0.10471326618337097,"score_gpt":0.34946216242534706,"score_spread":0.2447488962419761,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2084662104","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9986486,0.00025798782,0.00029953383,0.000092174916,0.0000015732849,0.0000039074766,0.000061306826,0.0000020852124,0.0006328821],"genre_scores_gemma":[0.99896777,0.00031053193,0.00039753792,0.000016844913,0.000004015245,0.0000065632175,0.00010389581,0.000002259978,0.00019051826],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9998348,0.000077335906,0.0000056111126,0.000044379238,0.000018603396,0.000019243325],"domain_scores_gemma":[0.9996729,0.00010346202,0.00010299608,0.000023845698,0.00004306223,0.00005380116],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00032864444,0.00010219397,0.0001321139,0.00044789253,0.0005647996,0.00045107753,0.00018330557,0.00013358015,0.00053675735],"category_scores_gemma":[0.0010624491,0.00007341331,0.000052434214,0.00077884557,0.00046075718,0.00013631865,0.00033845406,0.00018007864,0.00003931933],"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":[0.0000940403,0.00002005272,0.9810985,0.000020969024,0.000036675163,0.00019810963,0.0017875121,0.0005915178,0.0017525967,0.0008089288,0.00022461975,0.013366351],"study_design_scores_gemma":[0.000010252028,0.000039496776,0.9929301,0.00004127846,0.00003240638,0.00032938016,0.002288124,0.0011841148,0.00034920164,0.00071087823,0.0020780386,0.0000066340963],"about_ca_topic_score_codex":0.064137146,"about_ca_topic_score_gemma":0.12752686,"teacher_disagreement_score":0.064137146,"about_ca_system_score_codex":0.00043454682,"about_ca_system_score_gemma":0.00035198883,"threshold_uncertainty_score":0.12752765},"labels":[],"label_agreement":null},{"id":"W2085020944","doi":"10.1046/j.1469-1809.2003.00027.x","title":"Methylenetetrahydrofolate Reductase (<i>MTHFR</i>) Allele Frequencies in Amerindians","year":2003,"lang":"en","type":"article","venue":"Annals of Human Genetics","topic":"Folate and B Vitamins Research","field":"Medicine","cited_by":8,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Canadian Blood Services; University of British Columbia","funders":"Conselho Nacional de Desenvolvimento Científico e Tecnológico; Financiadora de Estudos e Projetos; Heart and Stroke Foundation of Canada; Foundation for the National Institutes of Health; National Science Foundation","keywords":"Methylenetetrahydrofolate reductase; Allele; Genetics; Allele frequency; Biology; Genotype; Homocysteine; Mutation; Methionine; Gene; Endocrinology; Amino acid","score_opus":0.10690332800595237,"score_gpt":0.391524159201915,"score_spread":0.28462083119596265,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2085020944","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9994949,0.00011008722,0.000032467753,0.000018500592,7.878037e-7,0.0000013695845,0.00005457061,0.000002596864,0.0002846695],"genre_scores_gemma":[0.9996381,0.00007197828,0.000041121926,0.000009658835,0.000002522028,0.0000017997393,0.000064525346,0.0000010657766,0.00016925411],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99991226,0.000023165181,0.0000065986706,0.00002585737,0.000013685065,0.000018397364],"domain_scores_gemma":[0.99981624,0.00003744536,0.00007523071,0.000012705247,0.000023733992,0.000034672867],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00009797264,0.000121720615,0.00013292147,0.00075111445,0.00018123051,0.00019833072,0.00013832713,0.00019872405,0.0018900944],"category_scores_gemma":[0.0006758686,0.00010279593,0.00008878114,0.00054745714,0.00022554664,0.00008873925,0.00015350661,0.00014753091,0.00022206166],"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":[0.00024186386,0.000031754356,0.98910356,0.000013781321,0.000036949237,0.00027051632,0.0006973738,0.00003463613,0.0039078724,0.000060434715,0.00015457158,0.005446773],"study_design_scores_gemma":[0.0000061097116,0.000062890605,0.99907494,0.000002451996,0.000011905069,0.00036151445,0.00015617497,0.000034507706,0.0001231936,0.000016498709,0.00014844307,0.000001339107],"about_ca_topic_score_codex":0.017541036,"about_ca_topic_score_gemma":0.012204137,"teacher_disagreement_score":0.017541036,"about_ca_system_score_codex":0.00017044369,"about_ca_system_score_gemma":0.00008273619,"threshold_uncertainty_score":0.034877896},"labels":[],"label_agreement":null},{"id":"W2089006329","doi":"10.1111/j.1469-1809.2000.ahg641_0089_4.x","title":"<i>Lionel Sharples Penrose: a Biography</i>. By M. S<scp>mith</scp>. Obtainable from The Lavenham Press, Water St., Lavenham, Sudbury CO10 9RN. £9.95, p+p £1.","year":2000,"lang":"en","type":"article","venue":"Annals of Human Genetics","topic":"Nutrition, Genetics, and Disease","field":"Biochemistry, Genetics and Molecular Biology","cited_by":0,"is_retracted":false,"has_abstract":false,"route_ca_aff":false,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":true,"ca_institutions":"","funders":"","keywords":"Biography; Annals; Citation; Combinatorics; Theology; Philosophy; Art; Art history; Classics; Mathematics; Computer science; World Wide Web","score_opus":0.020153450064759937,"score_gpt":0.2655996186303862,"score_spread":0.2454461685656263,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2089006329","genre_codex":"other","genre_gemma":"other","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"other","genre_consensus":"other","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.00080251106,0.31409597,0.0027190836,0.08085324,0.05410206,0.00008668707,0.0013779644,0.0014060095,0.54455656],"genre_scores_gemma":[0.0020275721,0.040113755,0.00078799424,0.0055640205,0.0028202988,0.000024400388,0.00027172035,0.00036401642,0.9480262],"study_design_codex":"not_applicable","study_design_gemma":"not_applicable","domain_scores_codex":[0.9995579,0.000088397785,0.000023643603,0.00008784446,0.0001950311,0.00004717017],"domain_scores_gemma":[0.9991949,0.00019288363,0.000050966606,0.00003908144,0.00028053642,0.00024157038],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00082695985,0.0013816989,0.00091328914,0.0020641428,0.0013078793,0.0023160416,0.00091639365,0.0010583617,0.2649412],"category_scores_gemma":[0.0018142409,0.00048577454,0.00032148894,0.0013960839,0.00068353396,0.002460253,0.0014594294,0.002830984,0.26211658],"study_design_candidate":"not_applicable","study_design_consensus":"not_applicable","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.000011878462,0.000006011106,0.000035175122,0.00007311868,0.0000011466446,0.000020858626,0.00005933083,0.000008133197,0.00008549133,0.0008848732,0.9599482,0.03886583],"study_design_scores_gemma":[7.7038095e-7,0.0000042803695,0.00010501079,0.00004345001,6.6797304e-7,0.00008035593,0.000043755354,0.000008170199,0.000044990597,0.00016780659,0.9994986,0.000002132991],"about_ca_topic_score_codex":0.004605749,"about_ca_topic_score_gemma":0.010741627,"teacher_disagreement_score":0.2649412,"about_ca_system_score_codex":0.0011292514,"about_ca_system_score_gemma":0.0007663227,"threshold_uncertainty_score":0.88631654},"labels":[],"label_agreement":null},{"id":"W2108492891","doi":"10.1111/j.1469-1809.2005.00255.x","title":"The role of Self‐Defined Race/Ethnicity in Population Structure Control","year":2006,"lang":"en","type":"article","venue":"Annals of Human Genetics","topic":"Genetic Associations and Epidemiology","field":"Biochemistry, Genetics and Molecular Biology","cited_by":26,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Lunenfeld-Tanenbaum Research Institute; Mount Sinai Hospital; University of Toronto; Hospital for Sick Children","funders":"National Cancer Institute","keywords":"Race (biology); Ethnic group; Population; Population control; Demography; Biology; Sociology; Anthropology; Research methodology","score_opus":0.01341136605609761,"score_gpt":0.28877087261824747,"score_spread":0.27535950656214986,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2108492891","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.8429337,0.010891115,0.12934904,0.006156791,0.0005532684,0.00026599836,0.00050278235,0.00012334109,0.009224017],"genre_scores_gemma":[0.9871781,0.00073886267,0.010867407,0.0005271724,0.00013061194,0.000054503314,0.00007866453,0.00002340073,0.00040128783],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.96601826,0.028116599,0.00083069614,0.0024702942,0.0019526025,0.00061146024],"domain_scores_gemma":[0.93863857,0.04123833,0.006480578,0.010180126,0.0023769166,0.0010855441],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0421744,0.0005713168,0.00095902476,0.0011753528,0.0011487866,0.0022933313,0.0014139264,0.00081887137,0.0010156421],"category_scores_gemma":[0.09092625,0.0003097937,0.00073547335,0.0015119569,0.0038514119,0.0019254916,0.0012384929,0.0012966187,0.00015870809],"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":[0.00064925436,0.0002447697,0.85974395,0.00016730698,0.0015529417,0.00027974593,0.003716602,0.0023065708,0.0021567545,0.036495022,0.0007320772,0.09195496],"study_design_scores_gemma":[0.00013462898,0.0008950464,0.88108826,0.00030483512,0.0015648126,0.00094696454,0.0013148052,0.031466573,0.004957492,0.06746326,0.009736089,0.00012717917],"about_ca_topic_score_codex":0.009268513,"about_ca_topic_score_gemma":0.010171145,"teacher_disagreement_score":0.0421744,"about_ca_system_score_codex":0.00069733796,"about_ca_system_score_gemma":0.0015840846,"threshold_uncertainty_score":0.22304219},"labels":[],"label_agreement":null},{"id":"W2111279973","doi":"10.1046/j.1529-8817.2005.00152.x","title":"Ethiopia: between Sub-Saharan Africa and Western Eurasia","year":2005,"lang":"en","type":"article","venue":"Annals of Human Genetics","topic":"Forensic and Genetic Research","field":"Biochemistry, Genetics and Molecular Biology","cited_by":35,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Université de Montréal; McGill University; Centre Hospitalier Universitaire Sainte-Justine","funders":"Canadian Institutes of Health Research","keywords":"Haplotype; Ethnic group; Population; Middle East; Context (archaeology); Geography; Gene flow; Gene pool; Out of africa; Allele; Locus (genetics); Biology; Demography; Evolutionary biology; Genetics; Genetic variation; Genetic diversity; Gene; Anthropology; Sociology","score_opus":0.07968463329335398,"score_gpt":0.3627551347700462,"score_spread":0.2830705014766922,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2111279973","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.97471976,0.009242098,0.0011363525,0.0003288587,0.0000663046,0.000053416592,0.00047575013,0.000022601427,0.013954792],"genre_scores_gemma":[0.994145,0.0022596915,0.0013785515,0.0002477485,0.000029344015,0.000024810068,0.0002147623,0.000007264372,0.0016928884],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9997905,0.000051889216,0.00001680296,0.000058582358,0.000026522344,0.000055726367],"domain_scores_gemma":[0.9998222,0.000034111636,0.00006447123,0.0000068808727,0.00003242927,0.000039884268],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0004391471,0.00039740835,0.00024039453,0.0009636796,0.0005284766,0.0014752495,0.00023867912,0.00019651232,0.0029690969],"category_scores_gemma":[0.00040356134,0.0001278156,0.00013174405,0.0011308009,0.00037271762,0.00074064743,0.0007362166,0.00026288218,0.00031569443],"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":[0.001759201,0.0003048663,0.671784,0.0012007663,0.00061967096,0.0043761404,0.008994418,0.00068703794,0.0746128,0.007855519,0.0018148676,0.2259908],"study_design_scores_gemma":[0.000060966966,0.00019479814,0.9471675,0.000363825,0.00017044996,0.0035003077,0.009357327,0.00024207418,0.004141591,0.0022074585,0.032570057,0.000023676721],"about_ca_topic_score_codex":0.0024817418,"about_ca_topic_score_gemma":0.0049249823,"teacher_disagreement_score":0.0029690969,"about_ca_system_score_codex":0.00037859424,"about_ca_system_score_gemma":0.00059417885,"threshold_uncertainty_score":0.009932578},"labels":[],"label_agreement":null},{"id":"W2117653622","doi":"10.1111/ahg.12034","title":"Quantitative Variation in Plasma Angiotensin‐I Converting Enzyme Activity Shows Allelic Heterogeneity in the <i>ABO</i> Blood Group Locus","year":2013,"lang":"en","type":"article","venue":"Annals of Human Genetics","topic":"Genetic Associations and Epidemiology","field":"Biochemistry, Genetics and Molecular Biology","cited_by":24,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"McGill University and Génome Québec Innovation Centre","funders":"BHF Centre of Research Excellence, Oxford; Ministry of Education, Culture, Sports, Science and Technology; Agence Nationale de la Recherche; British Heart Foundation; Wellcome Trust; McGill University; Takeda Science Foundation","keywords":"ABO blood group system; Allele; Genetics; Biology; Locus (genetics); Haplotype; Quantitative trait locus; Genetic variation; Population; Genetic architecture; Allelic heterogeneity; Gene; Medicine","score_opus":0.055366026020480893,"score_gpt":0.3215515469390212,"score_spread":0.2661855209185403,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2117653622","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9993457,0.000046723275,0.0003531895,0.0000100402,0.0000018389139,0.0000019447657,0.00006100039,0.0000052743503,0.00017424673],"genre_scores_gemma":[0.9995828,0.00002128638,0.00020598882,0.000011061147,0.0000034277505,0.0000022947738,0.00007463381,0.000004395824,0.00009404154],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99949646,0.00016245566,0.000037776303,0.00016022539,0.00009131719,0.000051828807],"domain_scores_gemma":[0.999419,0.00019250305,0.00019445672,0.000075027245,0.000037640755,0.00008147222],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00054484804,0.00024637775,0.00031108703,0.0005067808,0.00023626734,0.00040541956,0.00018218534,0.00023002963,0.0011985513],"category_scores_gemma":[0.0008424777,0.00015194273,0.00023215586,0.0005494056,0.00043014623,0.00009174885,0.00026091802,0.00031011604,0.00014427857],"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":[0.0010387909,0.000106763255,0.79844034,0.00004113857,0.00046294532,0.00056699343,0.00076236826,0.00016918896,0.18901666,0.00032475204,0.00022495935,0.008845133],"study_design_scores_gemma":[0.000013783917,0.000060235714,0.99796414,0.000002697256,0.00003648331,0.0003724969,0.00004480998,0.00020997178,0.0010787415,0.00008284995,0.00012800274,0.0000058310093],"about_ca_topic_score_codex":0.0038754612,"about_ca_topic_score_gemma":0.0037202323,"teacher_disagreement_score":0.0038754612,"about_ca_system_score_codex":0.00014034462,"about_ca_system_score_gemma":0.000090859045,"threshold_uncertainty_score":0.0077058077},"labels":[],"label_agreement":null},{"id":"W2118702967","doi":"10.1046/j.1469-1809.2000.6420135.x","title":"Beta<sub>2</sub>‐adrenergic receptor allele frequencies in the Quechua, a high altitude native population","year":2000,"lang":"en","type":"article","venue":"Annals of Human Genetics","topic":"Neuroscience of respiration and sleep","field":"Neuroscience","cited_by":17,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":true,"ca_institutions":"University of British Columbia","funders":"Natural Sciences and Engineering Research Council of Canada; Heart and Stroke Foundation of Canada","keywords":"Allele; Biology; Genetics; Allele frequency; Population; Linkage disequilibrium; Gene; Haplotype; Demography","score_opus":0.07565418479140414,"score_gpt":0.3202396722745523,"score_spread":0.24458548748314818,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2118702967","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99953854,0.00005960234,0.00006587928,0.000007346985,0.0000010036656,0.0000036362517,0.0000863017,0.000001804167,0.00023595855],"genre_scores_gemma":[0.9996176,0.000040363047,0.000064876345,0.0000066929324,0.0000017540868,0.0000024504795,0.000063017666,7.781457e-7,0.00020246123],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99988616,0.00002191361,0.000006623427,0.000045066758,0.000016318332,0.00002386744],"domain_scores_gemma":[0.9998405,0.00003416787,0.000045342582,0.000013345551,0.000028225308,0.000038412745],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00014491571,0.00018639577,0.00015785656,0.0007029407,0.0003882933,0.00033918748,0.00015962066,0.00020417667,0.0013831188],"category_scores_gemma":[0.000420735,0.00008107279,0.000106230545,0.0005130258,0.00038371186,0.000120326906,0.00012907566,0.000128814,0.00012667493],"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":[0.00031026793,0.000048904603,0.97831476,0.000013231578,0.00009319585,0.00057920895,0.0013586342,0.00010091752,0.012784823,0.00012885101,0.00010634949,0.0061607864],"study_design_scores_gemma":[0.0000076226906,0.00008812132,0.99864846,0.0000028407117,0.000018334184,0.0002880753,0.00039096942,0.0001287629,0.0002202656,0.000021944275,0.00018005386,0.000004650259],"about_ca_topic_score_codex":0.12844151,"about_ca_topic_score_gemma":0.13118897,"teacher_disagreement_score":0.12844151,"about_ca_system_score_codex":0.0005222141,"about_ca_system_score_gemma":0.00016200889,"threshold_uncertainty_score":0.25538778},"labels":[],"label_agreement":null},{"id":"W2129437279","doi":"10.1046/j.1469-1809.2003.00043.x","title":"Selective Pressure has not Acted Against Hypercoagulability Alleles in High‐Altitude Amerindians","year":2003,"lang":"en","type":"article","venue":"Annals of Human Genetics","topic":"Blood properties and coagulation","field":"Medicine","cited_by":6,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Canadian Blood Services; University of British Columbia","funders":"Heart and Stroke Foundation of Canada","keywords":"Allele; Biology; Genetics; Fibrinogen; Allele frequency; Gene; Effects of high altitude on humans; Hematocrit; Endocrinology","score_opus":0.08668193901691605,"score_gpt":0.3162936402862172,"score_spread":0.22961170126930114,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2129437279","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9994166,0.00009588433,0.000060679726,0.000044786273,0.0000029227663,0.0000011418745,0.000012530069,0.0000015940818,0.00036388362],"genre_scores_gemma":[0.9996238,0.000048771868,0.000050725655,0.000029704355,0.0000060834304,9.529645e-7,0.000018697943,0.0000016971718,0.00021955518],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9998405,0.00003356425,0.000008861757,0.000037166556,0.000026425176,0.000053435688],"domain_scores_gemma":[0.99975306,0.00006416946,0.0000667218,0.000023168584,0.000035893412,0.000057045094],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0002487537,0.00012756161,0.00016080397,0.00031656757,0.0003423411,0.00027560213,0.00020054492,0.00017220649,0.0018833329],"category_scores_gemma":[0.0006017172,0.000060251732,0.00013972745,0.0002910938,0.00056247343,0.00013238034,0.00015091237,0.0001836427,0.00011066541],"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":[0.0013970447,0.000084840154,0.8195856,0.000057467838,0.00029206966,0.0016187327,0.0019502372,0.0002688153,0.14675109,0.0011719192,0.0003276854,0.026494423],"study_design_scores_gemma":[0.000055586144,0.00019203492,0.9941203,0.000011087835,0.00006827647,0.0011052248,0.0005120433,0.00021291772,0.0023783073,0.00021290839,0.0011217254,0.000009536842],"about_ca_topic_score_codex":0.014394339,"about_ca_topic_score_gemma":0.025063446,"teacher_disagreement_score":0.014394339,"about_ca_system_score_codex":0.00030589526,"about_ca_system_score_gemma":0.00032069397,"threshold_uncertainty_score":0.028621137},"labels":[],"label_agreement":null},{"id":"W2140906093","doi":"10.1111/j.1469-1809.2011.00668.x","title":"A Replication Study of the IRS1, CAPN10, TCF7L2, and PPARG Gene Polymorphisms Associated with Type 2 Diabetes in Two Different Populations of Mexico","year":2011,"lang":"en","type":"article","venue":"Annals of Human Genetics","topic":"Peroxisome Proliferator-Activated Receptors","field":"Biochemistry, Genetics and Molecular Biology","cited_by":59,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Toronto","funders":"Instituto Mexicano del Seguro Social","keywords":"TCF7L2; Peroxisome proliferator-activated receptor gamma; Type 2 diabetes; Single-nucleotide polymorphism; Genetics; Biology; Type 2 Diabetes Mellitus; Internal medicine; Diabetes mellitus; Gene; Genotype; Endocrinology; Medicine; Peroxisome proliferator-activated receptor","score_opus":0.07343149739810038,"score_gpt":0.3181278339311928,"score_spread":0.24469633653309242,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2140906093","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":"reproducibility","model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":"reproducibility","domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9986481,0.00010944941,0.0004975002,0.00003566427,0.000008266327,0.00006566792,0.00036161544,0.00000703147,0.000266683],"genre_scores_gemma":[0.99760216,0.0000955379,0.00068385934,0.00006647223,0.00001527576,0.00013576366,0.0008336179,0.0000087033095,0.00055868976],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9991597,0.00027829333,0.000047238653,0.00033692928,0.0000984154,0.00007947987],"domain_scores_gemma":[0.9989588,0.000192386,0.00026145414,0.0003251724,0.00016773053,0.000094421244],"candidate_categories":["metaresearch"],"consensus_categories":[],"category_scores_codex":[0.001616256,0.00081689766,0.0005719098,0.0006491616,0.0012315179,0.00054717046,0.00062135875,0.0006205586,0.0013092657],"category_scores_gemma":[0.0027324816,0.0004214373,0.00086064846,0.0007218307,0.0004246991,0.00014852417,0.00049465604,0.0005600212,0.0001919815],"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":[0.0017539831,0.00029639722,0.98470193,0.000038515456,0.00085578486,0.0007098715,0.0008224361,0.000082222825,0.005546713,0.00008761786,0.0004697709,0.0046348297],"study_design_scores_gemma":[0.00037584873,0.0004011862,0.99654007,0.000011647826,0.00047864165,0.00056248927,0.00026038042,0.00013820737,0.00042494934,0.00003629659,0.00076251914,0.000007719438],"about_ca_topic_score_codex":0.02384031,"about_ca_topic_score_gemma":0.018628338,"teacher_disagreement_score":0.99838376,"about_ca_system_score_codex":0.0005349236,"about_ca_system_score_gemma":0.00049974606,"threshold_uncertainty_score":0.047403097},"labels":[],"label_agreement":null},{"id":"W2153637912","doi":"10.1046/j.1469-1809.2003.00004.x","title":"Genetic Polymorphisms in the Renin‐Angiotensin System in High‐Altitude and Low‐Altitude Native American Populations","year":2003,"lang":"en","type":"article","venue":"Annals of Human Genetics","topic":"Genetics and Physical Performance","field":"Biochemistry, Genetics and Molecular Biology","cited_by":53,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Canadian Blood Services; University of British Columbia; Earl Haig Secondary School; University of British Columbia Hospital","funders":"","keywords":"Genetics; Biology; Allele; Population; Locus (genetics); Gene; Effects of high altitude on humans; Medicine","score_opus":0.03141917796926441,"score_gpt":0.30094686028738393,"score_spread":0.2695276823181195,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2153637912","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99964666,0.000085661326,0.000068104986,0.000008979023,0.0000012649894,0.000004071781,0.000030301344,0.0000011948373,0.00015376748],"genre_scores_gemma":[0.9996567,0.000065805994,0.0000887334,0.000010624874,0.0000037648322,0.000003979991,0.000045753295,5.0829595e-7,0.00012407596],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9997973,0.00006948732,0.000014751479,0.0000496132,0.000042245105,0.000026645406],"domain_scores_gemma":[0.9997391,0.00008071416,0.00006403309,0.000018527804,0.000033254993,0.00006436273],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00023982949,0.0001628421,0.00014243647,0.0005312349,0.00030780735,0.00030908713,0.00015299357,0.00021608062,0.0007837476],"category_scores_gemma":[0.000784998,0.00010150005,0.00011804217,0.0005327287,0.00032931278,0.00012985476,0.00015356796,0.00020885421,0.00007214672],"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":[0.0002847184,0.00012317384,0.9893222,0.000015322545,0.00009373245,0.00039505173,0.00072458835,0.00006784508,0.0050591393,0.000073608564,0.000053956966,0.0037866891],"study_design_scores_gemma":[0.000013671878,0.00012648324,0.9988154,0.0000025727459,0.00002248137,0.00036970075,0.00024518595,0.00011334315,0.00013961537,0.00003995994,0.00010860954,0.000003063252],"about_ca_topic_score_codex":0.011538538,"about_ca_topic_score_gemma":0.010872144,"teacher_disagreement_score":0.011538538,"about_ca_system_score_codex":0.00015945651,"about_ca_system_score_gemma":0.00013733382,"threshold_uncertainty_score":0.022942722},"labels":[],"label_agreement":null},{"id":"W2155239124","doi":"10.1046/j.1469-1809.2002.00121.x","title":"Multifunctional zinc finger proteins in development and disease","year":2002,"lang":"en","type":"review","venue":"Annals of Human Genetics","topic":"Renal and related cancers","field":"Biochemistry, Genetics and Molecular Biology","cited_by":119,"is_retracted":false,"has_abstract":true,"route_ca_aff":false,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"","funders":"Canadian Institutes of Health Research","keywords":"Zinc finger; LIM domain; Biology; Proteome; RING finger domain; Computational biology; Gene; RNA splicing; Alternative splicing; Zinc finger nuclease; Genetics; DNA-binding protein; PHD finger; Transcription factor; Human proteome project; Cell biology; RNA; Proteomics; Exon","score_opus":0.08146836149446776,"score_gpt":0.3374126197579988,"score_spread":0.25594425826353107,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2155239124","genre_codex":"review","genre_gemma":"review","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"review","genre_consensus":"review","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.00018444778,0.9975031,0.00016754474,0.00045016452,0.0002860734,0.0000027008223,0.000007687208,0.000012035825,0.0013862301],"genre_scores_gemma":[0.0021629995,0.9942585,0.00031949749,0.000405102,0.00047261623,0.0000058494907,0.000025932326,0.0000018430408,0.0023477592],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.9998448,0.000027304268,0.000020568166,0.000029103574,0.000059395643,0.000018837995],"domain_scores_gemma":[0.9998148,0.00006563751,0.000024531368,0.000010214841,0.000046029003,0.00003876423],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0005727341,0.0009204,0.0011348997,0.0014239128,0.0003377776,0.0007581847,0.0008237876,0.001303924,0.0027299854],"category_scores_gemma":[0.00051552657,0.00018636095,0.00022244923,0.0016733293,0.00081357785,0.0011199436,0.00066627894,0.0011678393,0.0025982463],"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":[0.00009354689,0.000046426077,0.0005227987,0.0034518407,0.00004850123,0.0006829006,0.000094535484,0.00032866656,0.0022902584,0.0060049477,0.055613503,0.930822],"study_design_scores_gemma":[0.0000145856,0.000037443933,0.0011002236,0.0007102328,0.000026295826,0.0028098614,0.000048334623,0.000050905397,0.00030746116,0.0041062436,0.99077916,0.000009318168],"about_ca_topic_score_codex":0.0009010212,"about_ca_topic_score_gemma":0.0015157192,"teacher_disagreement_score":0.0027299854,"about_ca_system_score_codex":0.00083945546,"about_ca_system_score_gemma":0.0008907294,"threshold_uncertainty_score":0.009132683},"labels":[],"label_agreement":null},{"id":"W2302845675","doi":"10.1111/ahg.12150","title":"Importance of Genetic Studies in Consanguineous Populations for the Characterization of Novel Human Gene Functions","year":2016,"lang":"en","type":"review","venue":"Annals of Human Genetics","topic":"Hemoglobinopathies and Related Disorders","field":"Medicine","cited_by":44,"is_retracted":false,"has_abstract":true,"route_ca_aff":false,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"","funders":"Institute of Nutrition, Metabolism and Diabetes; Medical Research Council; King Saud University","keywords":"Biology; Genetics; Disease gene identification; Gene; Genome; Phenotype; Consanguinity; Genetic heterogeneity; Loss function; Offspring; Exome sequencing; Pregnancy","score_opus":0.2626356238057638,"score_gpt":0.4409816982109659,"score_spread":0.17834607440520212,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2302845675","genre_codex":"review","genre_gemma":"review","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"review","genre_consensus":"review","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.00016182823,0.99742293,0.0003803506,0.0010388651,0.00023616076,0.000004950876,0.00002337441,0.00000973561,0.00072173175],"genre_scores_gemma":[0.0011764279,0.99672395,0.0009694634,0.00039247004,0.00040371704,0.000008111064,0.00004252067,0.0000034431744,0.00027991313],"study_design_codex":"design_other","study_design_gemma":"systematic_review","domain_scores_codex":[0.99946755,0.00018541072,0.00007358282,0.000095280935,0.00015594205,0.000022123995],"domain_scores_gemma":[0.99694496,0.002216627,0.00019556924,0.000111362846,0.0004072493,0.00012414185],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0021464424,0.00067377364,0.0015292655,0.0026843268,0.00022646265,0.00096127106,0.000836288,0.0013367579,0.0020553528],"category_scores_gemma":[0.002445781,0.00018781802,0.000590514,0.0017689874,0.0011330039,0.0015510087,0.0006323005,0.0026472015,0.0012212488],"study_design_candidate":"systematic_review","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.000063620486,0.000053728752,0.0016663006,0.01034385,0.00015444755,0.00057586306,0.00011307559,0.00021504561,0.0031254746,0.00459712,0.0163365,0.96275496],"study_design_scores_gemma":[0.000030233397,0.0001154651,0.010163536,0.009071695,0.00035317094,0.008554933,0.00027787325,0.0001260672,0.0012774053,0.008401571,0.96156913,0.00005895783],"about_ca_topic_score_codex":0.0011184344,"about_ca_topic_score_gemma":0.0013153402,"teacher_disagreement_score":0.0026843268,"about_ca_system_score_codex":0.00055034034,"about_ca_system_score_gemma":0.0012743117,"threshold_uncertainty_score":0.011351585},"labels":[],"label_agreement":null},{"id":"W2573625654","doi":"10.1111/ahg.12182","title":"No Evidence for Association of β‐Defensin Genomic Copy Number with HIV Susceptibility, HIV Load during Clinical Latency, or Progression to AIDS","year":2017,"lang":"en","type":"article","venue":"Annals of Human Genetics","topic":"HIV Research and Treatment","field":"Immunology and Microbiology","cited_by":4,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Manitoba; Public Health Agency of Canada","funders":"Schweizerischer Nationalfonds zur Förderung der Wissenschaftlichen Forschung; International AIDS Vaccine Initiative","keywords":"Defensin; Copy-number variation; Biology; Beta defensin; Viral load; Latency (audio); Human immunodeficiency virus (HIV); Genetics; Single-nucleotide polymorphism; Immunology; Gene; Genome; Genotype","score_opus":0.15068511749676664,"score_gpt":0.45737495998706673,"score_spread":0.30668984249030007,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2573625654","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9987179,0.00037629652,0.00023722994,0.00003554001,0.000005493948,0.0000024374594,0.00012456915,0.000004096121,0.0004964673],"genre_scores_gemma":[0.99958116,0.00007722609,0.00008733595,0.00001265327,0.0000068563295,0.0000014559346,0.00009597753,0.0000019837205,0.00013538047],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9994012,0.00020798834,0.000049662645,0.00017864109,0.000104956096,0.000057498746],"domain_scores_gemma":[0.99603134,0.0021908318,0.00092014525,0.00041266176,0.00016957738,0.00027551365],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0008898727,0.00020825844,0.00028837594,0.00070575456,0.00030724207,0.0005452182,0.0003605612,0.00047016804,0.004837027],"category_scores_gemma":[0.0037768108,0.00018252492,0.00041346194,0.0006028857,0.00058133295,0.000311534,0.00036848374,0.00032072637,0.00029124675],"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":[0.00040659143,0.000020645884,0.9905709,0.00002506519,0.0002597458,0.00020436523,0.00015905192,0.000075912474,0.00482466,0.00008820919,0.000053722404,0.003311197],"study_design_scores_gemma":[0.000010628647,0.00024632545,0.99657947,0.000012330423,0.00009834566,0.0015175868,0.00016458226,0.00023266443,0.0006752794,0.0001406955,0.00031659025,0.000005630246],"about_ca_topic_score_codex":0.0005634986,"about_ca_topic_score_gemma":0.00062569726,"teacher_disagreement_score":0.004837027,"about_ca_system_score_codex":0.00010549685,"about_ca_system_score_gemma":0.000114925475,"threshold_uncertainty_score":0.016181469},"labels":[],"label_agreement":null},{"id":"W2615015571","doi":"10.1046/j.1469-1809.2004.00146.x","title":"Analysis of Y‐chromosome Variability and its Comparison with mtDNA Variability Reveals Different Demographic Histories Between Islands in the Azores Archipelago (Portugal)","year":2005,"lang":"en","type":"article","venue":"Annals of Human Genetics","topic":"Forensic and Genetic Research","field":"Biochemistry, Genetics and Molecular Biology","cited_by":22,"is_retracted":false,"has_abstract":true,"route_ca_aff":false,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"","funders":"Fundação para a Ciência e a Tecnologia; Canadian Immunization Research Network","keywords":"Haplogroup; Archipelago; Human mitochondrial DNA haplogroup; Mitochondrial DNA; Geography; Population; Biology; Mainland; Demography; Evolutionary biology; Zoology; Genetics; Haplotype; Ecology; Allele","score_opus":0.04457682102567142,"score_gpt":0.33356295874200376,"score_spread":0.28898613771633236,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2615015571","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99966526,0.00006948079,0.00002930577,0.000003625576,3.979325e-7,0.0000011617559,0.000043693042,4.4890942e-7,0.00018666961],"genre_scores_gemma":[0.9995869,0.00006085768,0.00009852361,0.000003502953,0.0000017806359,0.0000017641019,0.00013914504,6.9898886e-7,0.000106730666],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99986374,0.000033888668,0.000010921898,0.000036542857,0.000026990176,0.000027900232],"domain_scores_gemma":[0.99980944,0.00003752504,0.000080256985,0.00001569077,0.000027635528,0.000029500014],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00031048586,0.00012944937,0.00015576684,0.0009140261,0.00032546002,0.00034397963,0.00013969015,0.0001159482,0.000621764],"category_scores_gemma":[0.00051814417,0.00006538671,0.00012796682,0.00048495492,0.0003084966,0.000088399895,0.00030215216,0.00009461064,0.000087951055],"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":[0.00014425357,0.000019562556,0.9861287,0.000017037042,0.00006565043,0.00013685894,0.001061156,0.000070006514,0.0060457373,0.000059012375,0.000044022974,0.0062080687],"study_design_scores_gemma":[0.0000010140084,0.000013008849,0.99952924,0.0000025471757,0.0000046734194,0.00006455364,0.0001790247,0.000029641076,0.00008035042,0.0000052995483,0.000090095025,6.4799315e-7],"about_ca_topic_score_codex":0.01415974,"about_ca_topic_score_gemma":0.020013984,"teacher_disagreement_score":0.01415974,"about_ca_system_score_codex":0.00013573625,"about_ca_system_score_gemma":0.000108115935,"threshold_uncertainty_score":0.028154612},"labels":[],"label_agreement":null},{"id":"W2615828161","doi":"10.1046/j.1469-1809.2005.00152.x","title":"Ethiopia: between Sub‐Saharan Africa and Western Eurasia","year":2005,"lang":"en","type":"article","venue":"Annals of Human Genetics","topic":"Forensic and Genetic Research","field":"Biochemistry, Genetics and Molecular Biology","cited_by":25,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Université de Montréal; McGill University; Centre Hospitalier Universitaire Sainte-Justine","funders":"","keywords":"Haplotype; Ethnic group; Middle East; Population; Context (archaeology); Gene flow; Geography; Out of africa; Gene pool; Allele; Locus (genetics); Population genetics; Evolutionary biology; Demography; Biology; Genetics; Genetic variation; Genetic diversity; Gene; Anthropology; Sociology","score_opus":0.08114172502008392,"score_gpt":0.36437852043509983,"score_spread":0.2832367954150159,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2615828161","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.977113,0.008834305,0.00053022534,0.0002850803,0.000049325274,0.00003541164,0.00034383123,0.000011174596,0.012797689],"genre_scores_gemma":[0.99550617,0.002407075,0.0007791117,0.00014092286,0.000023862174,0.000014614824,0.00017276887,0.0000037165066,0.0009517311],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99981624,0.000052228002,0.000013909819,0.000043381657,0.000020217294,0.000053956916],"domain_scores_gemma":[0.99980587,0.000050171748,0.00006389987,0.000006959917,0.00003588316,0.00003724013],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00045701218,0.00036205832,0.0002186136,0.0012231161,0.00040609803,0.0013848197,0.00019544497,0.0001547889,0.0031636835],"category_scores_gemma":[0.00040532797,0.00010700688,0.0001216749,0.0015399681,0.00035658,0.00063959515,0.00060556526,0.000227927,0.00020845154],"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":[0.0012895516,0.00019168956,0.74721885,0.0011528486,0.00056610664,0.0044986946,0.007946702,0.00068078487,0.03392395,0.0062961197,0.0014218596,0.19481291],"study_design_scores_gemma":[0.00006263338,0.00014346087,0.95445156,0.00044404573,0.00017693375,0.0029379425,0.012386564,0.00030093367,0.0020148999,0.0021047725,0.024953537,0.000022654041],"about_ca_topic_score_codex":0.0036628381,"about_ca_topic_score_gemma":0.0061329654,"teacher_disagreement_score":0.0036628381,"about_ca_system_score_codex":0.00034758332,"about_ca_system_score_gemma":0.00062580314,"threshold_uncertainty_score":0.010583639},"labels":[],"label_agreement":null},{"id":"W2731481699","doi":"10.1111/ahg.12202","title":"Differentiating the Cochran‐Armitage Trend Test and Pearson's χ<sup>2</sup> Test: Location and Dispersion","year":2017,"lang":"en","type":"article","venue":"Annals of Human Genetics","topic":"Genetic Associations and Epidemiology","field":"Biochemistry, Genetics and Molecular Biology","cited_by":17,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Gilead Sciences (Canada)","funders":"National Center for Advancing Translational Sciences; National Institutes of Health","keywords":"Dispersion (optics); Statistics; Mathematics; Test (biology); Pearson's chi-squared test; Standard deviation; Pearson product-moment correlation coefficient; Inheritance (genetic algorithm); Statistical hypothesis testing; Genetics; Biology; Physics; Test statistic; Optics; Ecology","score_opus":0.03883722517346953,"score_gpt":0.32223545655575486,"score_spread":0.2833982313822853,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2731481699","genre_codex":"methods","genre_gemma":"methods","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"methods","genre_consensus":"methods","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.26369786,0.0059777,0.7031399,0.00618599,0.0011834328,0.00039070396,0.0015360189,0.001541422,0.016347025],"genre_scores_gemma":[0.83467966,0.0012003811,0.15736751,0.0011733338,0.0009310151,0.00045405907,0.00072955014,0.00044410038,0.0030203995],"study_design_codex":"design_other","study_design_gemma":"theoretical_or_conceptual","domain_scores_codex":[0.96309525,0.024391137,0.0027348706,0.002779061,0.00621528,0.00078437757],"domain_scores_gemma":[0.65552324,0.30865642,0.015108554,0.009959576,0.0090117855,0.0017404638],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.045240365,0.00096324174,0.0014592,0.005840418,0.00056502735,0.0028776352,0.0018641098,0.002510686,0.0055036545],"category_scores_gemma":[0.24191545,0.00046987302,0.0011213025,0.00579866,0.0035564983,0.0029142243,0.002086803,0.0029501698,0.0014453455],"study_design_candidate":"theoretical_or_conceptual","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0019285274,0.00020560257,0.36759824,0.001006947,0.0011726328,0.003225643,0.0016397932,0.014881964,0.004969136,0.1300727,0.020953435,0.4523454],"study_design_scores_gemma":[0.00022876315,0.0020663452,0.3739485,0.000856399,0.0007050891,0.010787908,0.0033426543,0.1891148,0.013434295,0.36454368,0.04029031,0.00068129785],"about_ca_topic_score_codex":0.001778991,"about_ca_topic_score_gemma":0.0013974779,"teacher_disagreement_score":0.045240365,"about_ca_system_score_codex":0.00090088433,"about_ca_system_score_gemma":0.0018372419,"threshold_uncertainty_score":0.23925674},"labels":[],"label_agreement":null},{"id":"W2805805479","doi":"10.1111/ahg.12257","title":"Decomposing Pearson's χ<sup>2</sup> test: A linear regression and its departure from linearity","year":2018,"lang":"en","type":"article","venue":"Annals of Human Genetics","topic":"Genetic Associations and Epidemiology","field":"Biochemistry, Genetics and Molecular Biology","cited_by":5,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Gilead Sciences (Canada)","funders":"National Center for Advancing Translational Sciences; National Institutes of Health","keywords":"Mathematics; Statistics; Test statistic; Statistic; Pearson's chi-squared test; Linear regression; F-test; Regression analysis; Goodness of fit; Linear model; Regression dilution; Regression; Statistical hypothesis testing; Polynomial regression","score_opus":0.050496621525056753,"score_gpt":0.35254522702045893,"score_spread":0.3020486054954022,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2805805479","genre_codex":"methods","genre_gemma":"methods","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"methods","genre_consensus":"methods","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.03085801,0.00038738002,0.9638359,0.0013423194,0.00011641122,0.0000997892,0.00013340975,0.000428636,0.0027981903],"genre_scores_gemma":[0.7205553,0.00035840287,0.27397996,0.0010033743,0.00038537118,0.00060188246,0.00028865034,0.0003487058,0.0024784906],"study_design_codex":"theoretical_or_conceptual","study_design_gemma":"theoretical_or_conceptual","domain_scores_codex":[0.9226668,0.05688711,0.002995163,0.006478761,0.009782852,0.0011893371],"domain_scores_gemma":[0.5836213,0.37721267,0.010665132,0.020336745,0.0069965585,0.0011675542],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.07837706,0.0011819048,0.0014577924,0.003261547,0.00082073256,0.0027777848,0.003272931,0.0019922394,0.003350933],"category_scores_gemma":[0.2658984,0.00078672153,0.0013590779,0.0031911114,0.009664642,0.00425833,0.0028501237,0.0050157285,0.0009941482],"study_design_candidate":"theoretical_or_conceptual","study_design_consensus":"theoretical_or_conceptual","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0007266866,0.00020586418,0.07838561,0.0006813077,0.00082353054,0.0034880424,0.0017292645,0.07582132,0.009137098,0.6302116,0.0065756557,0.19221401],"study_design_scores_gemma":[0.00005221425,0.000543612,0.023436768,0.00016944544,0.00017219443,0.0023097396,0.0005748048,0.52594334,0.0067451256,0.43424103,0.005681141,0.00013054739],"about_ca_topic_score_codex":0.002271776,"about_ca_topic_score_gemma":0.0010010989,"teacher_disagreement_score":0.07837706,"about_ca_system_score_codex":0.0018449314,"about_ca_system_score_gemma":0.0025628058,"threshold_uncertainty_score":0.41450244},"labels":[],"label_agreement":null},{"id":"W2922471749","doi":"10.1111/ahg.12307","title":"Genetic studies of multiple consanguineous Pakistani families segregating oculocutaneous albinism identified novel and reported mutations","year":2019,"lang":"en","type":"article","venue":"Annals of Human Genetics","topic":"melanin and skin pigmentation","field":"Biochemistry, Genetics and Molecular Biology","cited_by":10,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Toronto; Centre for Addiction and Mental Health","funders":"Higher Education Commision, Pakistan; Higher Education Commission, Pakistan","keywords":"Oculocutaneous albinism; Genetics; Sanger sequencing; Biology; Albinism; Exome sequencing; Genotyping; Disease gene identification; Consanguinity; Genetic heterogeneity; Mutation; Gene; Hypopigmentation; Single-nucleotide polymorphism; Genotype; Phenotype","score_opus":0.068898295086688,"score_gpt":0.36046774504399753,"score_spread":0.29156944995730955,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2922471749","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99886405,0.00018362861,0.00035196473,0.000026873238,0.0000072674466,0.000014462446,0.00009517237,0.000006429618,0.00045025477],"genre_scores_gemma":[0.9990061,0.00018690748,0.00041590168,0.000033581044,0.000008231548,0.0000075842186,0.00010171815,0.000004038649,0.00023608918],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9995159,0.000056639892,0.00004949264,0.0002165121,0.00010084489,0.000060769442],"domain_scores_gemma":[0.99948525,0.00018068621,0.00012600968,0.000036317208,0.00006654711,0.00010506888],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00030389536,0.0008386856,0.00037960178,0.0012074969,0.000908224,0.00031342427,0.00028220756,0.00038909164,0.002134759],"category_scores_gemma":[0.0010147778,0.000231397,0.00039038144,0.0010055922,0.00063203264,0.00016590206,0.00046349317,0.0003211486,0.00019622342],"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":[0.0010394248,0.0002158137,0.68182206,0.00017485746,0.0004522565,0.14030357,0.0050712163,0.0002966137,0.13667752,0.0006586518,0.00049065484,0.03279737],"study_design_scores_gemma":[0.00012835872,0.0004783417,0.79777247,0.000052056297,0.00038566696,0.1761103,0.0015325294,0.0009392255,0.017947828,0.00025664386,0.0043302444,0.00006624736],"about_ca_topic_score_codex":0.004265374,"about_ca_topic_score_gemma":0.00418458,"teacher_disagreement_score":0.004265374,"about_ca_system_score_codex":0.00038864216,"about_ca_system_score_gemma":0.00029150845,"threshold_uncertainty_score":0.008481085},"labels":[],"label_agreement":null},{"id":"W2978543468","doi":"10.1111/ahg.12357","title":"Xq26 duplications lead to undergrowth or overgrowth via competing pathways including GPC3/GPC4","year":2019,"lang":"en","type":"article","venue":"Annals of Human Genetics","topic":"Glycosylation and Glycoproteins Research","field":"Biochemistry, Genetics and Molecular Biology","cited_by":3,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"McGill University Health Centre; Montreal Children's Hospital; McGill University","funders":"Institut de recherche, Centre universitaire de santé McGill","keywords":"Undergrowth; Lead (geology); Genetics; Biology; Evolutionary biology; Paleontology; Ecology","score_opus":0.10434709213425343,"score_gpt":0.3732946296751739,"score_spread":0.2689475375409205,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2978543468","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9951379,0.0009500172,0.0016284855,0.00019774676,0.000017100416,0.000016542754,0.0001671862,0.00008051188,0.0018046487],"genre_scores_gemma":[0.99656576,0.00058112055,0.0010119035,0.00006933793,0.000018398918,0.000008903927,0.00015028444,0.000017682125,0.0015765508],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.99983215,0.000028023214,0.000015723526,0.00005121898,0.000034813183,0.000038005914],"domain_scores_gemma":[0.9998318,0.0000467865,0.000068395035,0.000012010428,0.000008493909,0.000032486103],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.000115921226,0.0010629877,0.0002480056,0.00052151945,0.00043813977,0.00019864942,0.00018817867,0.0005110703,0.0029221561],"category_scores_gemma":[0.0003578632,0.0002586194,0.00028567258,0.00035932945,0.0006553918,0.00019947792,0.0005353244,0.0004517841,0.00034347005],"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":[0.00091157824,0.000091079826,0.06340085,0.00020711719,0.00016259699,0.2326013,0.0006092426,0.001229675,0.67335904,0.0037086469,0.0009375457,0.022781318],"study_design_scores_gemma":[0.0001358974,0.00042585697,0.2090077,0.000047698515,0.00019705752,0.5422826,0.0003293546,0.0023286184,0.22985305,0.0016305838,0.013723,0.000038685128],"about_ca_topic_score_codex":0.0010398766,"about_ca_topic_score_gemma":0.0010419367,"teacher_disagreement_score":0.0029221561,"about_ca_system_score_codex":0.00033501428,"about_ca_system_score_gemma":0.00025975294,"threshold_uncertainty_score":0.009775579},"labels":[],"label_agreement":null},{"id":"W2985175171","doi":"10.1111/ahg.12364","title":"Improved assembly and variant detection of a haploid human genome using single‐molecule, high‐fidelity long reads","year":2019,"lang":"en","type":"article","venue":"Annals of Human Genetics","topic":"Genomics and Phylogenetic Studies","field":"Biochemistry, Genetics and Molecular Biology","cited_by":144,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of British Columbia; BC Cancer Agency","funders":"U.S. National Library of Medicine; National Institute of General Medical Sciences; National Human Genome Research Institute; H2020 European Research Council; Howard Hughes Medical Institute; National Institutes of Health; National Science Foundation","keywords":"Genome; Human genome; Structural variation; Sequence assembly; Segmental duplication; Hybrid genome assembly; Computational biology; Biology; Tandem repeat; Fidelity; DNA sequencing; Gene duplication; Sequence (biology); Genetics; Gene; Computer science; Gene family","score_opus":0.03786177443747611,"score_gpt":0.2881192018732974,"score_spread":0.2502574274358213,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2985175171","genre_codex":"empirical","genre_gemma":"methods","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"methods","genre_consensus":null,"domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.5202287,0.0010200265,0.46760795,0.0002754435,0.00008230085,0.00013402452,0.0055066515,0.0032658826,0.0018791624],"genre_scores_gemma":[0.4632772,0.00037000934,0.5248575,0.00009572061,0.000019621319,0.00007862717,0.00924892,0.0004902804,0.001562146],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9991584,0.00021466456,0.0000681585,0.00031001325,0.00020008764,0.000048718863],"domain_scores_gemma":[0.99880767,0.0004843723,0.00017370723,0.00029501767,0.00018661942,0.00005261067],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0014439196,0.00037036632,0.00052573567,0.0005187078,0.00029671344,0.00072432484,0.00044083776,0.00045455006,0.0013013775],"category_scores_gemma":[0.003249625,0.00046397262,0.0005322838,0.00044199912,0.00020995636,0.00040208045,0.00050766394,0.00068595243,0.0007015403],"study_design_candidate":"bench_or_experimental","study_design_consensus":"bench_or_experimental","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00029549378,0.00003181924,0.006972118,0.00025588076,0.00009109165,0.00021846252,0.00033696042,0.005585178,0.94723874,0.0015513265,0.0008154703,0.036607347],"study_design_scores_gemma":[0.000050254654,0.00026606876,0.039155524,0.00005233023,0.00010741624,0.0011122025,0.00014742152,0.080193914,0.860237,0.0010873406,0.017508296,0.00008234115],"about_ca_topic_score_codex":0.0016347226,"about_ca_topic_score_gemma":0.003373432,"teacher_disagreement_score":0.0016347226,"about_ca_system_score_codex":0.00039995246,"about_ca_system_score_gemma":0.0004429914,"threshold_uncertainty_score":0.0076363087},"labels":[],"label_agreement":null},{"id":"W4224211592","doi":"10.1111/ahg.12467","title":"No significant association between SNPs in the <i>CLOCK</i> and <i>ADH4</i> genes and susceptibility to cluster headaches: A systematic review and meta‐analysis","year":2022,"lang":"en","type":"review","venue":"Annals of Human Genetics","topic":"Migraine and Headache Studies","field":"Medicine","cited_by":2,"is_retracted":false,"has_abstract":true,"route_ca_aff":false,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":true,"ca_institutions":"","funders":"National Natural Science Foundation of China","keywords":"Single-nucleotide polymorphism; Odds ratio; Internal medicine; Biology; Genetics; Bioinformatics; Medicine; Genotype; Gene","score_opus":0.23404330239690893,"score_gpt":0.42301110265349706,"score_spread":0.18896780025658813,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4224211592","genre_codex":"review","genre_gemma":"review","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"review","genre_consensus":"review","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.007924867,0.98879915,0.0007682219,0.00042331987,0.00024120098,0.00033831838,0.0011370998,0.00003185762,0.00033594805],"genre_scores_gemma":[0.33903027,0.6510227,0.0027134567,0.0021307706,0.00056761346,0.0019180293,0.002059393,0.00005699087,0.00050090667],"study_design_codex":"meta_analysis","study_design_gemma":"meta_analysis","domain_scores_codex":[0.99028975,0.0040162057,0.0031315237,0.001278369,0.0008935934,0.00039045207],"domain_scores_gemma":[0.9722206,0.021259898,0.0038464773,0.0007876491,0.0015852698,0.000300067],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.016022388,0.002183935,0.015683187,0.004481806,0.0007210084,0.003181422,0.002336775,0.0021827144,0.0041013295],"category_scores_gemma":[0.036185466,0.0012680589,0.029274141,0.0064932294,0.0009966675,0.0015614012,0.0013888256,0.0014396206,0.00031758114],"study_design_candidate":"meta_analysis","study_design_consensus":"meta_analysis","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0017235442,0.000017239905,0.008540662,0.38059074,0.59876096,0.00016766258,0.00011416729,0.00032835384,0.0003088991,0.00014799123,0.000978844,0.008321046],"study_design_scores_gemma":[0.00046409128,0.00011832911,0.0050228373,0.017921804,0.97476554,0.000089458365,0.00004032731,0.000103965096,0.00007831346,0.00017390317,0.0012056442,0.000015784844],"about_ca_topic_score_codex":0.006429074,"about_ca_topic_score_gemma":0.013419912,"teacher_disagreement_score":0.016022388,"about_ca_system_score_codex":0.0022175994,"about_ca_system_score_gemma":0.0041558533,"threshold_uncertainty_score":0.08473545},"labels":[],"label_agreement":null},{"id":"W4224229333","doi":"10.1111/ahg.12469","title":"A novel leaky splice variant in centromere protein J (<i>CENPJ</i>)‐associated Seckel syndrome","year":2022,"lang":"en","type":"article","venue":"Annals of Human Genetics","topic":"Microtubule and mitosis dynamics","field":"Biochemistry, Genetics and Molecular Biology","cited_by":0,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Lunenfeld-Tanenbaum Research Institute","funders":"Department of Biotechnology, Ministry of Science and Technology, India","keywords":"Microcephaly; Biology; Genetics; Sanger sequencing; Exon; Exome sequencing; splice; Alternative splicing; Exome; RNA splicing; Gene; Mutation; RNA","score_opus":0.025484070835042404,"score_gpt":0.271586431189061,"score_spread":0.2461023603540186,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4224229333","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9983651,0.00018438548,0.0008470432,0.000062339255,0.000014759542,0.0000113457745,0.000093600414,0.000049913604,0.00037142588],"genre_scores_gemma":[0.9988456,0.00011757641,0.00046348563,0.000036620924,0.000013130056,0.000004285188,0.00008788507,0.000010840662,0.00042054564],"study_design_codex":"case_report","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99988365,0.000008428054,0.000013700983,0.000048490056,0.000024740308,0.0000209042],"domain_scores_gemma":[0.9997805,0.000050990395,0.00007492302,0.000017613811,0.0000132647765,0.000062743486],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.000067411944,0.0005708647,0.0003699081,0.00040838614,0.0002694753,0.00022891206,0.00024998814,0.0004955329,0.0015891138],"category_scores_gemma":[0.00037129378,0.0001636968,0.00025531172,0.00032194718,0.0004573508,0.00013237302,0.0003102116,0.00038088864,0.00028252872],"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":[0.0003355489,0.0000722078,0.032762777,0.00012274188,0.0000664574,0.66197693,0.00047113627,0.00031390818,0.2943261,0.00051722315,0.00038768604,0.00864739],"study_design_scores_gemma":[0.000054759512,0.00037158284,0.11632902,0.00001918866,0.00010149503,0.829176,0.00019140456,0.0010531528,0.0499661,0.00036019747,0.0023478286,0.000029339404],"about_ca_topic_score_codex":0.0005891507,"about_ca_topic_score_gemma":0.0009207175,"teacher_disagreement_score":0.0015891138,"about_ca_system_score_codex":0.00017734358,"about_ca_system_score_gemma":0.00018239878,"threshold_uncertainty_score":0.0053161383},"labels":[],"label_agreement":null},{"id":"W4249146063","doi":"10.1046/j.1469-1809.2001.6540387.x","title":"Grade‐of‐membership sibpair linkage analysis maps <i>IDDM11</i> to chromosome 14q24.3–q31","year":2001,"lang":"en","type":"article","venue":"Annals of Human Genetics","topic":"Genetic Associations and Epidemiology","field":"Biochemistry, Genetics and Molecular Biology","cited_by":15,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of British Columbia","funders":"National Institute on Aging; Medical Research Council; Medical Research Council Canada","keywords":"Haplotype; Genetics; Allele; Locus (genetics); Biology; Genetic linkage; Sibling; Linkage (software); Chromosome; Lod score; Gene mapping; Gene; Psychology","score_opus":0.0658191528399681,"score_gpt":0.3448509141452327,"score_spread":0.27903176130526464,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4249146063","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9901688,0.00008457923,0.007435701,0.000051621104,0.00000962751,0.000028809724,0.00059029466,0.000033390552,0.001597121],"genre_scores_gemma":[0.993922,0.000032907985,0.004803206,0.000012556748,0.0000043565674,0.000027517004,0.0004732858,0.000009638083,0.00071459933],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9993212,0.0003267498,0.000027984917,0.0001448415,0.00012213882,0.000057127352],"domain_scores_gemma":[0.9992204,0.0002291246,0.00022816604,0.0001524072,0.00005753667,0.000112395704],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00086059107,0.00039037195,0.00024249489,0.001180096,0.00037815038,0.00039181966,0.0004513044,0.00025846757,0.0062473486],"category_scores_gemma":[0.0021022083,0.00013194306,0.0003036014,0.0006493918,0.00025366375,0.00015955901,0.0006409929,0.00043204628,0.00056472665],"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":[0.0008691939,0.00018476031,0.90279746,0.000098578115,0.0003147594,0.0004067282,0.0007689336,0.0009860999,0.035091624,0.0022760958,0.0017908096,0.054414995],"study_design_scores_gemma":[0.00006580294,0.00059393665,0.9702064,0.000018609933,0.00012326585,0.0024183472,0.00024016132,0.008580039,0.0077323667,0.0023916378,0.0075965403,0.00003311239],"about_ca_topic_score_codex":0.0020093904,"about_ca_topic_score_gemma":0.0040627667,"teacher_disagreement_score":0.0062473486,"about_ca_system_score_codex":0.00018571508,"about_ca_system_score_gemma":0.00014053023,"threshold_uncertainty_score":0.020899415},"labels":[],"label_agreement":null},{"id":"W4412491844","doi":"10.1111/ahg.70011","title":"The Fortunes of Genomic Medicine: A Quarter Century of Promise","year":2025,"lang":"en","type":"article","venue":"Annals of Human Genetics","topic":"BRCA gene mutations in cancer","field":"Biochemistry, Genetics and Molecular Biology","cited_by":1,"is_retracted":false,"has_abstract":true,"route_ca_aff":false,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":true,"ca_institutions":"","funders":"Wellcome Trust","keywords":"Quarter (Canadian coin); Genomic medicine; Biology; Medicine; Genetics; History; Computational biology","score_opus":0.028042956275608356,"score_gpt":0.344179370642735,"score_spread":0.31613641436712664,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4412491844","genre_codex":"commentary","genre_gemma":"review","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"review","genre_consensus":null,"domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.0049623544,0.106449485,0.003574454,0.85389453,0.0040648463,0.000013184528,0.000045358593,0.0000347859,0.02696089],"genre_scores_gemma":[0.588948,0.14467545,0.006968291,0.22697672,0.019185053,0.00017802115,0.000103485974,0.0002073927,0.012757562],"study_design_codex":"theoretical_or_conceptual","study_design_gemma":"theoretical_or_conceptual","domain_scores_codex":[0.9603726,0.029468799,0.0010199725,0.001980742,0.0055994103,0.001558524],"domain_scores_gemma":[0.89715266,0.08891254,0.0020476778,0.004865042,0.0040964475,0.0029256872],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.041519903,0.00072608225,0.0012754605,0.0024595228,0.009716484,0.023535289,0.0017576732,0.0132246455,0.005030332],"category_scores_gemma":[0.05710455,0.00067402155,0.00072401285,0.002922277,0.09195865,0.033737496,0.008685858,0.018181693,0.0010242879],"study_design_candidate":"theoretical_or_conceptual","study_design_consensus":"theoretical_or_conceptual","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.000058435555,0.000014949782,0.00019820256,0.00033741636,0.000015351989,0.00020675184,0.021861756,0.00021235294,0.0001800625,0.929696,0.02501513,0.022203488],"study_design_scores_gemma":[0.000026169751,0.000040883606,0.00036559635,0.001539611,0.000013144866,0.00028149938,0.01864281,0.00023567787,0.00013690814,0.6429498,0.3357201,0.000047821446],"about_ca_topic_score_codex":0.0045559146,"about_ca_topic_score_gemma":0.0036421951,"teacher_disagreement_score":0.041519903,"about_ca_system_score_codex":0.012446692,"about_ca_system_score_gemma":0.011553569,"threshold_uncertainty_score":0.21958083},"labels":[],"label_agreement":null},{"id":"W4412519569","doi":"10.1111/ahg.70013","title":"Inherited Susceptibility to Cancer: Past, Present and Future","year":2025,"lang":"en","type":"review","venue":"Annals of Human Genetics","topic":"Genetic factors in colorectal cancer","field":"Medicine","cited_by":6,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Institute of Cancer Research; McGill University","funders":"NIHR Cambridge Biomedical Research Centre; National Institute for Health and Care Research; Department of Health and Social Care; Cancer Research UK","keywords":"Cancer; Genetics; Biology; Evolutionary biology","score_opus":0.12876598600644962,"score_gpt":0.4477592162618068,"score_spread":0.3189932302553572,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4412519569","genre_codex":"review","genre_gemma":"review","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"review","genre_consensus":"review","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.008110766,0.88165313,0.000948312,0.09949662,0.0016188839,0.0000073499073,0.0002744907,0.000043935728,0.007846529],"genre_scores_gemma":[0.07675024,0.8983541,0.001834843,0.014070919,0.0062156375,0.000026709511,0.00032346093,0.000021631547,0.002402402],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.999258,0.00021203469,0.00008006567,0.00016581183,0.00017410984,0.000109915214],"domain_scores_gemma":[0.9961623,0.0015762047,0.000524584,0.00014590238,0.00071096997,0.0008800557],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.002844876,0.00037135888,0.000717205,0.0017958499,0.000735522,0.0019440721,0.00062431797,0.0021789032,0.005150807],"category_scores_gemma":[0.00338503,0.00023388414,0.0004011524,0.0022137633,0.0024276692,0.002688897,0.0012445089,0.0025731518,0.00065340626],"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":[0.00041061672,0.00013757662,0.039663866,0.0031765576,0.00020525913,0.0011972276,0.0012053928,0.00043739448,0.00077154726,0.033851985,0.06838886,0.8505537],"study_design_scores_gemma":[0.00004910392,0.0003789313,0.1100383,0.012687103,0.0003981162,0.010307162,0.005693722,0.000943694,0.0003914113,0.07324942,0.7856925,0.00017047551],"about_ca_topic_score_codex":0.0070184455,"about_ca_topic_score_gemma":0.01001046,"teacher_disagreement_score":0.0070184455,"about_ca_system_score_codex":0.0023027358,"about_ca_system_score_gemma":0.002434778,"threshold_uncertainty_score":0.017231107},"labels":[],"label_agreement":null},{"id":"W4413770310","doi":"10.1111/ahg.70020","title":"Professor David Hopkinson (26 June 1935–22 March 2025). Former Editor‐in‐Chief of the <i>Annals of Human Genetics</i> ; in Memoriam Tribute","year":2025,"lang":"en","type":"article","venue":"Annals of Human Genetics","topic":"Nutrition, Genetics, and Disease","field":"Biochemistry, Genetics and Molecular Biology","cited_by":0,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Institute of Cancer Research","funders":"","keywords":"Annals; Tribute; Editor in chief; Classics; Philosophy; History; Management; Art history; Economics","score_opus":0.03637253318276052,"score_gpt":0.3501854186066545,"score_spread":0.31381288542389396,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4413770310","genre_codex":"editorial","genre_gemma":"editorial","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"editorial","genre_consensus":"editorial","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.0005101689,0.028598513,0.001054813,0.2838459,0.61119324,0.00010744905,0.0024752864,0.00040780145,0.07180669],"genre_scores_gemma":[0.0074471664,0.02590651,0.0009922081,0.087017745,0.14008869,0.00014459415,0.0022271448,0.00046455767,0.7357114],"study_design_codex":"not_applicable","study_design_gemma":"not_applicable","domain_scores_codex":[0.9991696,0.00016924272,0.000064489206,0.00022238879,0.000266947,0.00010742846],"domain_scores_gemma":[0.9961361,0.0005479895,0.00022445594,0.00013995751,0.0013840989,0.0015672942],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0023323228,0.0006201994,0.0007225041,0.0012494101,0.0008325533,0.0023484107,0.00093143893,0.001975933,0.27279463],"category_scores_gemma":[0.011770636,0.00031051456,0.00039575322,0.00040858125,0.0006265216,0.001191142,0.0016855242,0.002783939,0.16350314],"study_design_candidate":"not_applicable","study_design_consensus":"not_applicable","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.000017955994,0.000002254697,0.000056235505,0.000027926957,0.0000017923392,0.000036585254,0.0000056916383,0.000007936602,0.000022878492,0.0002640834,0.98564535,0.013911277],"study_design_scores_gemma":[0.000010183864,0.000011635462,0.0002894805,0.00012231311,0.0000027069198,0.00024345987,0.000028809254,0.0000208415,0.00004265234,0.00037508312,0.99884784,0.0000050872795],"about_ca_topic_score_codex":0.0032349022,"about_ca_topic_score_gemma":0.0072003393,"teacher_disagreement_score":0.27279463,"about_ca_system_score_codex":0.0010097797,"about_ca_system_score_gemma":0.0018026266,"threshold_uncertainty_score":0.91258895},"labels":[],"label_agreement":null}]}