{"meta":{"page":1,"per_page":50,"max_per_page":100,"total":48,"total_is_capped":false,"direct_labels_cover":0,"predictions_cover":48,"direct_label_status":"direct model label, unvalidated","prediction_status":"machine_predicted_unvalidated (Codex and Gemma teacher distillation)","score_status":"score_only:v0-immature-baseline (scores rank; they never assert a category)","snapshot":{"source":"OpenAlex, pinned release, all 482 partitions","release":"2026-06-24","frame_built":"2026-07-12"},"query_hash":"7190a6837033","filters":{"venue":"Genetic Testing"}},"results":[{"id":"W1966045468","doi":"10.1089/109065701753145538","title":"Universal Newborn Screening for Hb H Disease in California","year":2001,"lang":"en","type":"article","venue":"Genetic Testing","topic":"Hemoglobinopathies and Related Disorders","field":"Medicine","cited_by":106,"is_retracted":false,"has_abstract":true,"routes":{"ca_aff":true,"ca_fund":false,"ca_venue":false,"about_ca":false},"ca_institutions":"McMaster University","funders":"","keywords":"Newborn screening; Hemoglobinopathy; Medicine; Hydrops fetalis; Pediatrics; Thalassemia; Disease; Genotyping; Alpha-thalassemia; Pregnancy; Internal medicine; Genotype; Gestation; Biology; Genetics","retraction":null,"screen_n_in":null,"score":{"opus":0.02812692052816177,"gpt":0.2586477545833479,"spread":0.2305208340551861,"validation_status":"score_only:v0-immature-baseline"},"prediction":{"model_version":"codex-gemma-dda1882f352a","candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00008340421,0.00009888552,0.0001312582,0.0000850267,0.00007613935,0.000009697076,0.000049112,0.00005680542,0.00002863116],"category_scores_gemma":[0.0004967831,0.00009155575,0.0000456995,0.0002937656,0.00003251541,0.00001804648,0.00002476607,0.000112543,0.00001380387],"about_ca_system_candidate":false,"about_ca_system_consensus":false,"about_ca_system_score_codex":0.00003425985,"about_ca_system_score_gemma":0.0001072415,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_topic_score_codex":0.0001783583,"about_ca_topic_score_gemma":0.00001634903,"domain_scores_codex":[0.99921,0.00001319097,0.0001768473,0.0001956901,0.0000984178,0.0003058808],"domain_scores_gemma":[0.9994943,0.0000956034,0.00003810747,0.00013146,0.00004931818,0.0001911855],"domain_codex":null,"domain_gemma":null,"domain_candidate":null,"domain_consensus":null,"study_design_codex":"observational","study_design_gemma":"observational","study_design_scores_codex":[0.0001475136,0.00005858524,0.7192377,0.00005955546,0.00001207027,0.0003011213,0.00009953065,0.004790838,0.0006701152,0.000008720365,0.000188281,0.274426],"study_design_scores_gemma":[0.004832271,0.0002480017,0.7722265,0.000582066,0.0001634002,0.0001011029,0.0006138201,0.1739998,0.00003559761,0.0003255363,0.04657735,0.0002946166],"study_design_candidate":"observational","study_design_consensus":"observational","genre_codex":"empirical","genre_gemma":"empirical","genre_scores_codex":[0.9724696,0.0008359583,0.02337287,0.001000527,0.00006259759,0.0004449305,0.00001171723,0.00008916759,0.00171268],"genre_scores_gemma":[0.914869,0.00003816987,0.08424581,0.0003219234,0.0001225633,0.0000131199,0.00001875566,0.00002762829,0.0003430331],"genre_candidate":"empirical","genre_consensus":"empirical","teacher_disagreement_score":0.2741314,"threshold_uncertainty_score":0.3733535,"prediction_status":"machine_predicted_unvalidated"},"labels":[],"label_agreement":null},{"id":"W1974892673","doi":"10.1089/gte.2005.9.231","title":"Initial Screening Transferrin Saturation Values, Serum Ferritin Concentrations, and <i>HFE</i> Genotypes in Whites and Blacks in the Hemochromatosis and Iron Overload Screening Study","year":2005,"lang":"en","type":"article","venue":"Genetic Testing","topic":"Iron Metabolism and Disorders","field":"Medicine","cited_by":82,"is_retracted":false,"has_abstract":true,"routes":{"ca_aff":true,"ca_fund":false,"ca_venue":false,"about_ca":false},"ca_institutions":"London Health Sciences Centre; Western University","funders":"National Cancer Institute; National Heart, Lung, and Blood Institute; National Center for Research Resources; U.S. Public Health Service; Kaiser Permanente","keywords":"Transferrin saturation; Hemochromatosis; Hereditary hemochromatosis; Medicine; Internal medicine; Serum ferritin; Ferritin; Genotype; Serum iron; Transferrin; Genotyping; Gastroenterology; Anemia; Biology; Genetics","retraction":null,"screen_n_in":null,"score":{"opus":0.0239477026983767,"gpt":0.277414130024469,"spread":0.2534664273260923,"validation_status":"score_only:v0-immature-baseline"},"prediction":{"model_version":"codex-gemma-dda1882f352a","candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0004230101,0.000169234,0.0002275624,0.0001037982,0.0001599944,0.000089491,0.00004842279,0.00006436749,0.000007088726],"category_scores_gemma":[0.000221318,0.0001452357,0.00001318858,0.0002246564,0.00009121617,0.0001311338,0.00003034124,0.0002031177,3.952033e-7],"about_ca_system_candidate":false,"about_ca_system_consensus":false,"about_ca_system_score_codex":0.000009914982,"about_ca_system_score_gemma":0.00003293434,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_topic_score_codex":0.000426457,"about_ca_topic_score_gemma":0.0009038643,"domain_scores_codex":[0.9987193,0.0001624363,0.0003429005,0.0003100396,0.0002038742,0.000261405],"domain_scores_gemma":[0.9994938,0.0002444773,0.00004870684,0.0001212035,0.00002666041,0.00006511666],"domain_codex":null,"domain_gemma":null,"domain_candidate":null,"domain_consensus":null,"study_design_codex":"observational","study_design_gemma":"observational","study_design_scores_codex":[0.00005231692,0.00008729072,0.8324579,0.00006147552,0.000005013469,0.00001876115,0.00740016,0.0003283677,0.003492662,0.00001689597,0.00001072418,0.1560684],"study_design_scores_gemma":[0.003154693,0.0001894852,0.9821561,0.0001395641,0.00007971096,0.00008991358,0.008306603,0.005414182,0.0002596031,0.00002960758,0.00002655808,0.0001539803],"study_design_candidate":"observational","study_design_consensus":"observational","genre_codex":"empirical","genre_gemma":"empirical","genre_scores_codex":[0.9917559,0.006094161,0.0004292704,0.0006977829,0.00001586954,0.0007141796,0.000006138492,0.00002889273,0.0002577756],"genre_scores_gemma":[0.9818044,0.00014356,0.01737596,0.0005101866,0.0001140939,0.00002074284,0.000008734786,0.00001588939,0.000006374217],"genre_candidate":"empirical","genre_consensus":"empirical","teacher_disagreement_score":0.1559145,"threshold_uncertainty_score":0.5922539,"prediction_status":"machine_predicted_unvalidated"},"labels":[],"label_agreement":null},{"id":"W2045175397","doi":"10.1089/gte.2007.0057","title":"The Influence of Experiential Knowledge on Prenatal Screening and Testing Decisions","year":2008,"lang":"en","type":"article","venue":"Genetic Testing","topic":"Prenatal Screening and Diagnostics","field":"Medicine","cited_by":82,"is_retracted":false,"has_abstract":true,"routes":{"ca_aff":true,"ca_fund":false,"ca_venue":false,"about_ca":false},"ca_institutions":"Ottawa Hospital; Children's Hospital of Eastern Ontario; University of Ottawa","funders":"","keywords":"Experiential learning; Prenatal screening; Context (archaeology); Embodied cognition; Experiential knowledge; Psychology; Genetic testing; Qualitative research; Value (mathematics); Medicine; Applied psychology; Prenatal diagnosis; Pregnancy; Epistemology; Computer science; Artificial intelligence; Pedagogy; Sociology","retraction":null,"screen_n_in":null,"score":{"opus":0.06329573716192731,"gpt":0.2962395818875311,"spread":0.2329438447256038,"validation_status":"score_only:v0-immature-baseline"},"prediction":{"model_version":"codex-gemma-dda1882f352a","candidate_categories":["metaresearch"],"consensus_categories":[],"category_scores_codex":[0.0001522355,0.0001161864,0.0001554484,0.0000519282,0.0004489596,0.00001533305,0.0001092108,0.00004779308,0.000001433985],"category_scores_gemma":[0.01744433,0.00008721121,0.0000283699,0.0002886167,0.0002420189,0.00003058673,0.0001599303,0.00016504,0.000004902523],"about_ca_system_candidate":false,"about_ca_system_consensus":false,"about_ca_system_score_codex":0.000009392163,"about_ca_system_score_gemma":0.00008604677,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_topic_score_codex":0.00007625955,"about_ca_topic_score_gemma":0.000003879781,"domain_scores_codex":[0.9989974,0.00003204563,0.0002840858,0.0002186268,0.0002183023,0.0002495745],"domain_scores_gemma":[0.9944035,0.00489552,0.0001029923,0.000260107,0.0001983157,0.0001395353],"domain_codex":null,"domain_gemma":null,"domain_candidate":null,"domain_consensus":null,"study_design_codex":"design_other","study_design_gemma":"observational","study_design_scores_codex":[0.00009072435,0.00008772776,0.4436866,0.00003684458,0.00002572449,0.0001213028,0.001145647,0.004230255,0.007697092,0.00004623201,0.0001088846,0.5427229],"study_design_scores_gemma":[0.0006879914,0.0004847189,0.9859433,0.001084799,0.00003183816,0.0005964761,0.0001169736,0.006719574,0.004033753,0.00004948397,0.0001362216,0.0001148897],"study_design_candidate":"observational","study_design_consensus":null,"genre_codex":"empirical","genre_gemma":"empirical","genre_scores_codex":[0.9959198,0.001185392,0.001129664,0.00002705989,0.00004337513,0.0001599786,0.000004252686,0.00006463705,0.001465899],"genre_scores_gemma":[0.9261226,0.00002239562,0.07364996,0.00003054144,0.0001051931,0.00001150689,0.000001683959,0.00001458386,0.00004155187],"genre_candidate":"empirical","genre_consensus":"empirical","teacher_disagreement_score":0.5426081,"threshold_uncertainty_score":0.9908321,"prediction_status":"machine_predicted_unvalidated"},"labels":[],"label_agreement":null},{"id":"W2010447172","doi":"10.1089/gte.2007.0093","title":"The Prevalence of Consanguineous Marriages in an Underserved Area in Lebanon and Its Association with Congenital Anomalies","year":2008,"lang":"en","type":"article","venue":"Genetic Testing","topic":"Hemoglobinopathies and Related Disorders","field":"Medicine","cited_by":78,"is_retracted":false,"has_abstract":true,"routes":{"ca_aff":true,"ca_fund":false,"ca_venue":false,"about_ca":false},"ca_institutions":"York University","funders":"Ministry of Environment","keywords":"Consanguinity; Consanguineous Marriage; Demography; Cousin; Socioeconomic status; Population; Inbreeding; Medicine; Genetic counseling; Pediatrics; Environmental health; Geography; Genetics; Biology","retraction":null,"screen_n_in":null,"score":{"opus":0.02712721301691906,"gpt":0.231257764048267,"spread":0.2041305510313479,"validation_status":"score_only:v0-immature-baseline"},"prediction":{"model_version":"codex-gemma-dda1882f352a","candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.000151455,0.0000734385,0.0001242305,0.00004445462,0.00006185513,0.000006375556,0.00003712488,0.00006269267,0.000005499888],"category_scores_gemma":[0.0006155686,0.00005080314,0.000008924813,0.0001729718,0.00007005747,0.00002652948,0.00001458761,0.0001068175,4.468334e-7],"about_ca_system_candidate":false,"about_ca_system_consensus":false,"about_ca_system_score_codex":0.00003610399,"about_ca_system_score_gemma":0.00008453159,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_topic_score_codex":0.0001046813,"about_ca_topic_score_gemma":0.0003298997,"domain_scores_codex":[0.9993448,0.00005047891,0.000191742,0.0001272496,0.0001239085,0.0001617758],"domain_scores_gemma":[0.9994333,0.0002777549,0.00009332036,0.00008323479,0.00007737746,0.00003503582],"domain_codex":null,"domain_gemma":null,"domain_candidate":null,"domain_consensus":null,"study_design_codex":"observational","study_design_gemma":"observational","study_design_scores_codex":[0.00003645198,0.00003461102,0.9940706,0.00008229358,0.00001155915,0.00008044572,0.000806795,0.0001812439,0.003262301,0.000002911183,0.000004542546,0.001426167],"study_design_scores_gemma":[0.00106963,0.000356697,0.9930357,0.0001559034,0.00003204289,0.0001642955,0.0008840528,0.003681883,0.0005303521,0.00001719969,0.000005295445,0.00006691449],"study_design_candidate":"observational","study_design_consensus":"observational","genre_codex":"empirical","genre_gemma":"empirical","genre_scores_codex":[0.9951447,0.003889637,0.000002411339,0.000155747,0.00001910945,0.0002434779,0.000002540619,0.00001432878,0.0005280484],"genre_scores_gemma":[0.9989744,0.0003396765,0.0004105886,0.00002473628,0.000009367541,0.000006815479,0.000001158182,0.000007961073,0.0002253107],"genre_candidate":"empirical","genre_consensus":"empirical","teacher_disagreement_score":0.003829686,"threshold_uncertainty_score":0.2071692,"prediction_status":"machine_predicted_unvalidated"},"labels":[],"label_agreement":null},{"id":"W2060323966","doi":"10.1089/gte.2007.0024","title":"Evaluating Online Direct-to-Consumer Marketing of Genetic Tests: Informed Choices or Buyers Beware?","year":2008,"lang":"en","type":"article","venue":"Genetic Testing","topic":"BRCA gene mutations in cancer","field":"Biochemistry, Genetics and Molecular Biology","cited_by":72,"is_retracted":false,"has_abstract":true,"routes":{"ca_aff":true,"ca_fund":true,"ca_venue":false,"about_ca":false},"ca_institutions":"University of Calgary","funders":"National Human Genome Research Institute; National Institutes of Health; Genome Canada","keywords":"Genetic testing; Genetic counseling; Context (archaeology); The Internet; Mediation; Marketing; Test (biology); Commercialization; Business; Health care; Direct marketing; Medicine; Computer science; Economics","retraction":null,"screen_n_in":null,"score":{"opus":0.0711076731897278,"gpt":0.3545140028409268,"spread":0.2834063296511991,"validation_status":"score_only:v0-immature-baseline"},"prediction":{"model_version":"codex-gemma-dda1882f352a","candidate_categories":["metaresearch","metaepi_narrow"],"consensus_categories":[],"category_scores_codex":[0.0004101666,0.0002905327,0.0002905827,0.0001458868,0.0002388419,0.00002120484,0.0003964988,0.0001486029,0.00008001625],"category_scores_gemma":[0.008714284,0.0002795428,0.00008208943,0.000585897,0.0001620165,0.000006280401,0.0002685058,0.0001281308,0.00001379082],"about_ca_system_candidate":false,"about_ca_system_consensus":false,"about_ca_system_score_codex":0.00008637342,"about_ca_system_score_gemma":0.001031239,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_topic_score_codex":0.00009828396,"about_ca_topic_score_gemma":0.0001899676,"domain_scores_codex":[0.9976674,0.0001393216,0.0007367397,0.0005878917,0.0003682921,0.000500375],"domain_scores_gemma":[0.9979245,0.0005099286,0.0003533737,0.0006031609,0.0004445542,0.0001644766],"domain_codex":null,"domain_gemma":null,"domain_candidate":null,"domain_consensus":null,"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","study_design_scores_codex":[0.0001791493,0.0001028001,0.322128,0.0001796377,0.0001337291,0.00001756106,0.0005005553,0.03314032,0.480786,1.585432e-7,0.001095053,0.1617371],"study_design_scores_gemma":[0.001303966,0.0008225281,0.9292976,0.0003007666,0.0001140338,0.0003168821,0.0003341189,0.004550225,0.05569368,0.000006830603,0.006523522,0.0007358702],"study_design_candidate":"observational","study_design_consensus":null,"genre_codex":"empirical","genre_gemma":"empirical","genre_scores_codex":[0.9957039,0.001794451,0.0004053969,0.00004413935,0.0002129819,0.0004468176,0.00005212859,0.00004890285,0.001291278],"genre_scores_gemma":[0.7077764,0.0001232409,0.2909984,0.0002251356,0.0003185915,0.00007172381,0.00003436627,0.00005278747,0.0003993621],"genre_candidate":"empirical","genre_consensus":"empirical","teacher_disagreement_score":0.6071696,"threshold_uncertainty_score":0.9999657,"prediction_status":"machine_predicted_unvalidated"},"labels":[],"label_agreement":null},{"id":"W2176240200","doi":"10.1089/109065701753617471","title":"Detection of Severe Nondeletional <i>α</i> -Thalassemia Mutations Using a Single-Tube Multiplex ARMS Assay","year":2001,"lang":"en","type":"article","venue":"Genetic Testing","topic":"Hemoglobinopathies and Related Disorders","field":"Medicine","cited_by":66,"is_retracted":false,"has_abstract":true,"routes":{"ca_aff":true,"ca_fund":false,"ca_venue":false,"about_ca":false},"ca_institutions":"Hamilton Regional Laboratory Medicine Program; McMaster University Medical Centre","funders":"","keywords":"Thalassemia; Alpha-thalassemia; Mutation; Genetics; Hydrops fetalis; Biology; Multiplex; Multiplex polymerase chain reaction; Globin; Alpha globulin; Molecular biology; Gene; Polymerase chain reaction; Genotype; Fetus","retraction":null,"screen_n_in":null,"score":{"opus":0.03437432554801237,"gpt":0.2584638893874574,"spread":0.224089563839445,"validation_status":"score_only:v0-immature-baseline"},"prediction":{"model_version":"codex-gemma-dda1882f352a","candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0001363801,0.0001365003,0.0001910227,0.0001182663,0.0001279239,0.00001178876,0.00004701734,0.0001371341,0.00004436045],"category_scores_gemma":[0.0007007896,0.0001165735,0.00007521,0.00053065,0.00007497556,0.00003931455,0.00002519364,0.0001892992,0.00001039995],"about_ca_system_candidate":false,"about_ca_system_consensus":false,"about_ca_system_score_codex":0.00008408476,"about_ca_system_score_gemma":0.0001213174,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_topic_score_codex":0.0001551777,"about_ca_topic_score_gemma":0.00001506598,"domain_scores_codex":[0.9988731,0.00004187471,0.0003563085,0.0002246741,0.0002463169,0.0002577437],"domain_scores_gemma":[0.9991618,0.0001985639,0.0001495575,0.0001585227,0.0002287196,0.0001028593],"domain_codex":null,"domain_gemma":null,"domain_candidate":null,"domain_consensus":null,"study_design_codex":"bench_or_experimental","study_design_gemma":"simulation_or_modeling","study_design_scores_codex":[0.00002887053,0.0001679675,0.08773028,0.00006887592,0.00004226976,0.00005423042,0.0002681,0.02243284,0.8131685,0.000001235096,0.00001382701,0.07602295],"study_design_scores_gemma":[0.005862639,0.001000617,0.4095854,0.001310624,0.0007149442,0.009877856,0.002825224,0.521731,0.04404671,0.000462218,0.001768096,0.000814678],"study_design_candidate":"bench_or_experimental","study_design_consensus":null,"genre_codex":"empirical","genre_gemma":"empirical","genre_scores_codex":[0.9834282,0.0003182077,0.01404149,0.0001592916,0.0001402389,0.0002462415,0.000004769716,0.00008502228,0.001576536],"genre_scores_gemma":[0.9594145,0.00001331464,0.04022194,0.00008676484,0.0001148644,0.000006046262,0.00001214827,0.00002685125,0.000103597],"genre_candidate":"empirical","genre_consensus":"empirical","teacher_disagreement_score":0.7691218,"threshold_uncertainty_score":0.4753729,"prediction_status":"machine_predicted_unvalidated"},"labels":[],"label_agreement":null},{"id":"W2062506442","doi":"10.1089/gte.2006.9998","title":"Factors Associated with an Individual's Decision to Withdraw from Genetic Testing for Breast And Ovarian Cancer Susceptibility: Implications for Counseling","year":2007,"lang":"en","type":"article","venue":"Genetic Testing","topic":"BRCA gene mutations in cancer","field":"Biochemistry, Genetics and Molecular Biology","cited_by":62,"is_retracted":false,"has_abstract":true,"routes":{"ca_aff":true,"ca_fund":true,"ca_venue":false,"about_ca":false},"ca_institutions":"Université Laval; Université de Montréal","funders":"Canadian Institutes of Health Research; Canada Research Chairs","keywords":"Genetic testing; Breast cancer; Genetic counseling; Ovarian cancer; Confidentiality; Medicine; Test (biology); Cancer; Demography; Gynecology; Psychology; Family medicine; Internal medicine; Biology; Genetics","retraction":null,"screen_n_in":null,"score":{"opus":0.05848607298458652,"gpt":0.3232020614492286,"spread":0.2647159884646421,"validation_status":"score_only:v0-immature-baseline"},"prediction":{"model_version":"codex-gemma-dda1882f352a","candidate_categories":["metaepi_narrow"],"consensus_categories":[],"category_scores_codex":[0.0004588263,0.0002648402,0.0002092529,0.00008062705,0.0004209376,0.0001077615,0.0002430706,0.0001675293,0.000004068008],"category_scores_gemma":[0.001506319,0.0002525303,0.0000374561,0.000345366,0.00007842337,0.000008827619,0.00007931836,0.00007586801,2.139724e-7],"about_ca_system_candidate":false,"about_ca_system_consensus":false,"about_ca_system_score_codex":0.0001143699,"about_ca_system_score_gemma":0.0003578077,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_topic_score_codex":0.0002109377,"about_ca_topic_score_gemma":0.002871088,"domain_scores_codex":[0.9981175,0.00002965562,0.0003990041,0.0008095307,0.0001545545,0.0004897209],"domain_scores_gemma":[0.9976233,0.0008203894,0.00021066,0.0004301661,0.0006984645,0.0002170266],"domain_codex":null,"domain_gemma":null,"domain_candidate":null,"domain_consensus":null,"study_design_codex":"observational","study_design_gemma":"observational","study_design_scores_codex":[0.00007685034,0.00004911183,0.5519689,0.00001467589,0.0001011096,2.9502e-7,0.0003728947,0.006088867,0.2298519,0.000002931588,0.00005206251,0.2114204],"study_design_scores_gemma":[0.0009301971,0.000660015,0.9869444,0.000104546,0.0001612179,0.000008012204,0.0002657461,0.001508546,0.008263481,0.0005979727,0.0001654574,0.00039046],"study_design_candidate":"observational","study_design_consensus":"observational","genre_codex":"empirical","genre_gemma":"empirical","genre_scores_codex":[0.7985176,0.0003447693,0.1990897,0.00006692495,0.00008470791,0.0008730203,0.0009741149,0.00003996014,0.000009214707],"genre_scores_gemma":[0.7244875,0.00000212884,0.2746006,0.0001671828,0.0002737586,0.0001897727,0.0002130851,0.00005855653,0.000007347336],"genre_candidate":"empirical","genre_consensus":"empirical","teacher_disagreement_score":0.4349755,"threshold_uncertainty_score":0.9999927,"prediction_status":"machine_predicted_unvalidated"},"labels":[],"label_agreement":null},{"id":"W2081451187","doi":"10.1089/gte.2006.10.104","title":"No Evidence of <i>BRCA1/2</i> Genomic Rearrangements in High-Risk French-Canadian Breast/Ovarian Cancer Families","year":2006,"lang":"en","type":"article","venue":"Genetic Testing","topic":"BRCA gene mutations in cancer","field":"Biochemistry, Genetics and Molecular Biology","cited_by":52,"is_retracted":false,"has_abstract":true,"routes":{"ca_aff":true,"ca_fund":true,"ca_venue":false,"about_ca":true},"ca_institutions":"Alberta Children's Hospital; Hôtel-Dieu de Québec; Hôpital du Sacré-Cœur de Montréal; Cégep de Rimouski; Cégep de Jonquière; Université de Montréal; Université Laval; Hôpital du Saint-Sacrement; Centre Hospitalier Universitaire de Sherbrooke; Centre hospitalier universitaire de Québec","funders":"Canadian Institutes of Health Research; Canadian Breast Cancer Research Alliance; Canada Research Chairs; Breast Cancer Alliance","keywords":"Multiplex ligation-dependent probe amplification; Ovarian cancer; Biology; Genetics; Polymerase chain reaction; Breast cancer; Mutation; Southern blot; genomic DNA; Cancer; Gene; Oncology; Medicine; Exon","retraction":null,"screen_n_in":null,"score":{"opus":0.01384273038536755,"gpt":0.2429686627078576,"spread":0.22912593232249,"validation_status":"score_only:v0-immature-baseline"},"prediction":{"model_version":"codex-gemma-dda1882f352a","candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0002180716,0.0001847455,0.000173163,0.0001381624,0.00009171769,0.00002332578,0.0002981953,0.0001256214,0.00006386502],"category_scores_gemma":[0.0001898784,0.0002091167,0.00004415949,0.0003188169,0.000100825,0.000005892095,0.00009113589,0.0001091307,0.00001927868],"about_ca_system_candidate":false,"about_ca_system_consensus":false,"about_ca_system_score_codex":0.000189411,"about_ca_system_score_gemma":0.0007337511,"about_ca_topic_candidate":true,"about_ca_topic_consensus":true,"about_ca_topic_score_codex":0.4550805,"about_ca_topic_score_gemma":0.2425496,"domain_scores_codex":[0.9985101,0.00007617965,0.000400904,0.0004566065,0.0001522105,0.0004040342],"domain_scores_gemma":[0.99905,0.00004518119,0.0001899948,0.0004300041,0.0002020036,0.00008282695],"domain_codex":null,"domain_gemma":null,"domain_candidate":null,"domain_consensus":null,"study_design_codex":"observational","study_design_gemma":"observational","study_design_scores_codex":[0.00001235597,0.00002375988,0.636411,0.00004494835,0.00003115794,0.000005794177,0.00006160927,0.0151769,0.3151892,0.000004282606,0.001114983,0.03192404],"study_design_scores_gemma":[0.0005255194,0.000106118,0.9863046,0.0001560823,0.00003730053,0.00001617611,0.00002302591,0.0005453711,0.009962729,0.0001485856,0.001915436,0.0002590097],"study_design_candidate":"observational","study_design_consensus":"observational","genre_codex":"empirical","genre_gemma":"empirical","genre_scores_codex":[0.9930382,0.004185755,0.0002371164,0.00008494636,0.0002941076,0.0002462989,0.0001356925,0.00001172352,0.001766104],"genre_scores_gemma":[0.9795416,0.0002507863,0.01922474,0.0001100206,0.0004120045,0.00007628152,0.00002956417,0.00003377338,0.000321221],"genre_candidate":"empirical","genre_consensus":"empirical","teacher_disagreement_score":0.3498937,"threshold_uncertainty_score":0.852753,"prediction_status":"machine_predicted_unvalidated"},"labels":[],"label_agreement":null},{"id":"W2048226998","doi":"10.1089/gte.2007.0072","title":"New Mutations in the Wilson Disease Gene, <i>ATP7B</i> : Implications for Molecular Testing","year":2008,"lang":"en","type":"article","venue":"Genetic Testing","topic":"Trace Elements in Health","field":"Nursing","cited_by":52,"is_retracted":false,"has_abstract":true,"routes":{"ca_aff":true,"ca_fund":false,"ca_venue":false,"about_ca":false},"ca_institutions":"University of Alberta","funders":"","keywords":"Missense mutation; Wilson's disease; Ceruloplasmin; Genetics; Gene; Biology; Mutation; Phenotype; Genotype; Disease; Medicine; Internal medicine; Endocrinology","retraction":null,"screen_n_in":null,"score":{"opus":0.08191843773548349,"gpt":0.335725393249537,"spread":0.2538069555140535,"validation_status":"score_only:v0-immature-baseline"},"prediction":{"model_version":"codex-gemma-dda1882f352a","candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0002454858,0.0001635261,0.0001272725,0.0000928966,0.000589174,0.00004295039,0.0003261044,0.00003927984,0.000003107731],"category_scores_gemma":[0.00288163,0.0001552897,0.0000454774,0.0007685188,0.00004935276,0.00006481689,0.0000321055,0.000159317,0.000007443753],"about_ca_system_candidate":false,"about_ca_system_consensus":false,"about_ca_system_score_codex":0.00009380868,"about_ca_system_score_gemma":0.0002730447,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_topic_score_codex":0.0002984974,"about_ca_topic_score_gemma":0.00004372569,"domain_scores_codex":[0.9984038,0.0000979121,0.000431812,0.0003698372,0.0001872229,0.0005093603],"domain_scores_gemma":[0.9975041,0.001573237,0.0001585301,0.0004799907,0.0001179711,0.00016613],"domain_codex":null,"domain_gemma":null,"domain_candidate":null,"domain_consensus":null,"study_design_codex":"observational","study_design_gemma":"observational","study_design_scores_codex":[0.00002233839,0.0001498833,0.7517175,0.00009029712,0.000009004557,0.00002662301,0.001865496,0.02070533,0.02698437,0.0001833834,0.001596467,0.1966493],"study_design_scores_gemma":[0.0005469262,0.0001082335,0.9879919,0.00006240716,0.00005252919,0.00008037886,0.00007762096,0.004182893,0.0005917799,0.005489063,0.0006181276,0.0001981941],"study_design_candidate":"observational","study_design_consensus":"observational","genre_codex":"empirical","genre_gemma":"empirical","genre_scores_codex":[0.9455251,0.000826147,0.04474828,0.00636286,0.0002428321,0.001630996,0.0000460936,0.0002001425,0.0004176101],"genre_scores_gemma":[0.6633312,0.000001313454,0.335254,0.0009510021,0.0001866816,0.0002106144,0.00001758327,0.00003445424,0.00001316989],"genre_candidate":"empirical","genre_consensus":"empirical","teacher_disagreement_score":0.2905058,"threshold_uncertainty_score":0.6332528,"prediction_status":"machine_predicted_unvalidated"},"labels":[],"label_agreement":null},{"id":"W2040989154","doi":"10.1089/gte.2004.8.222","title":"Accuracy of Cancer Family Histories: Comparison of Two Breast Cancer Syndromes","year":2004,"lang":"en","type":"article","venue":"Genetic Testing","topic":"BRCA gene mutations in cancer","field":"Biochemistry, Genetics and Molecular Biology","cited_by":49,"is_retracted":false,"has_abstract":true,"routes":{"ca_aff":true,"ca_fund":false,"ca_venue":false,"about_ca":false},"ca_institutions":"Cancer Care Ontario","funders":"National Human Genome Research Institute; National Institutes of Health","keywords":"Medicine; Family history; Cancer; Medical diagnosis; Breast cancer; Cohort; Ovarian cancer; Genetic testing; Li–Fraumeni syndrome; Oncology; Internal medicine; Pathology; Genetics; Biology; Gene; Germline mutation","retraction":null,"screen_n_in":null,"score":{"opus":0.03931974102562871,"gpt":0.3476887180211113,"spread":0.3083689769954826,"validation_status":"score_only:v0-immature-baseline"},"prediction":{"model_version":"codex-gemma-dda1882f352a","candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0000719397,0.0001575754,0.0002481717,0.0000506205,0.00006067588,0.000007222224,0.0002446815,0.00007968531,0.00002949942],"category_scores_gemma":[0.0001395911,0.0001651447,0.0000628671,0.0002497204,0.0001601048,0.000003685262,0.00009745634,0.00007470846,0.000001185032],"about_ca_system_candidate":false,"about_ca_system_consensus":false,"about_ca_system_score_codex":0.000155146,"about_ca_system_score_gemma":0.0008666149,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_topic_score_codex":0.002846367,"about_ca_topic_score_gemma":0.0004486316,"domain_scores_codex":[0.9988359,0.00002396699,0.000428097,0.000304355,0.0001835416,0.0002241862],"domain_scores_gemma":[0.9988388,0.00004210111,0.0003795117,0.0003501118,0.0003361811,0.00005332862],"domain_codex":null,"domain_gemma":null,"domain_candidate":null,"domain_consensus":null,"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","study_design_scores_codex":[0.00001731486,0.00005987792,0.1684595,0.00008937863,0.00007810414,9.518945e-7,0.0004021756,0.06055798,0.7224988,0.00001533453,0.0002326094,0.04758804],"study_design_scores_gemma":[0.001864467,0.0002776524,0.3281958,0.0003369516,0.0001778815,0.0000488318,0.0005597761,0.0004286666,0.6644701,0.0002847002,0.002852625,0.0005024598],"study_design_candidate":"bench_or_experimental","study_design_consensus":"bench_or_experimental","genre_codex":"empirical","genre_gemma":"empirical","genre_scores_codex":[0.9799734,0.01766904,0.001262925,0.0001229537,0.000367602,0.0001577199,0.0001374242,0.00001426404,0.0002946701],"genre_scores_gemma":[0.9814167,0.0001861092,0.0179824,0.00006315911,0.0001958616,0.00006564393,0.00001147912,0.00002989623,0.0000487245],"genre_candidate":"empirical","genre_consensus":"empirical","teacher_disagreement_score":0.1597364,"threshold_uncertainty_score":0.6734407,"prediction_status":"machine_predicted_unvalidated"},"labels":[],"label_agreement":null},{"id":"W1981106753","doi":"10.1089/gte.2004.8.240","title":"Psychological Impact of Genetic Testing for Breast Cancer Susceptibility in Women of Ashkenazi Jewish Background: A Prospective Study","year":2004,"lang":"en","type":"article","venue":"Genetic Testing","topic":"BRCA gene mutations in cancer","field":"Biochemistry, Genetics and Molecular Biology","cited_by":46,"is_retracted":false,"has_abstract":true,"routes":{"ca_aff":false,"ca_fund":true,"ca_venue":false,"about_ca":false},"ca_institutions":"","funders":"National Health and Medical Research Council; Huntsman Cancer Institute; National Cancer Institute; National Medical Research Council; Cancer Care Ontario","keywords":"Medicine; Anxiety; Breast cancer; Judaism; Epidemiology; Genetic testing; Cancer; Gynecology; Psychiatry; Family medicine; Internal medicine","retraction":null,"screen_n_in":null,"score":{"opus":0.03820114396690552,"gpt":0.3538852049942379,"spread":0.3156840610273324,"validation_status":"score_only:v0-immature-baseline"},"prediction":{"model_version":"codex-gemma-dda1882f352a","candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0004003371,0.0002431973,0.0003535286,0.00008611236,0.00006170524,0.0000156593,0.0002862219,0.0001322108,0.00002130078],"category_scores_gemma":[0.0006200657,0.0002282729,0.0001011388,0.000551886,0.0001727901,0.000005223596,0.000127831,0.000119001,6.459642e-7],"about_ca_system_candidate":false,"about_ca_system_consensus":false,"about_ca_system_score_codex":0.0004942289,"about_ca_system_score_gemma":0.0005689777,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_topic_score_codex":0.000627705,"about_ca_topic_score_gemma":0.0003367969,"domain_scores_codex":[0.9979391,0.0000799218,0.000646297,0.0006843425,0.0001798096,0.0004705487],"domain_scores_gemma":[0.9984806,0.0001107168,0.0003286572,0.0004867565,0.0005086045,0.0000846662],"domain_codex":null,"domain_gemma":null,"domain_candidate":null,"domain_consensus":null,"study_design_codex":"observational","study_design_gemma":"observational","study_design_scores_codex":[0.0001430724,0.0005499808,0.714638,0.00004673478,0.00007116757,0.000002076729,0.0004549946,0.02542643,0.2332875,6.772038e-7,0.000006669761,0.02537271],"study_design_scores_gemma":[0.002388941,0.00309019,0.9876804,0.00006840319,0.00003106085,0.00004107153,0.000536394,0.0001757285,0.00492123,0.0008362614,9.895047e-7,0.0002293643],"study_design_candidate":"observational","study_design_consensus":"observational","genre_codex":"empirical","genre_gemma":"empirical","genre_scores_codex":[0.9969852,0.0005141628,0.0009002856,0.00001584372,0.00007887402,0.001250059,0.0001642723,0.00001591161,0.00007537273],"genre_scores_gemma":[0.9629117,0.000005799625,0.03638899,0.0000204255,0.0001591887,0.0004663374,0.000004521848,0.00003634232,0.000006704683],"genre_candidate":"empirical","genre_consensus":"empirical","teacher_disagreement_score":0.2730424,"threshold_uncertainty_score":0.9308701,"prediction_status":"machine_predicted_unvalidated"},"labels":[],"label_agreement":null},{"id":"W2028417643","doi":"10.1089/109065700316417","title":"Sensitivity of Multiple Color Spectral Karyotyping in Detecting Small Interchromosomal Rearrangements","year":2000,"lang":"en","type":"article","venue":"Genetic Testing","topic":"Genomic variations and chromosomal abnormalities","field":"Biochemistry, Genetics and Molecular Biology","cited_by":44,"is_retracted":false,"has_abstract":true,"routes":{"ca_aff":true,"ca_fund":true,"ca_venue":false,"about_ca":false},"ca_institutions":"McMaster University Medical Centre; London Health Sciences Centre","funders":"McMaster University","keywords":"Subtelomere; Sky; Karyotype; Biology; Chromosomal translocation; Fluorescence in situ hybridization; Fish <Actinopterygii>; Genetics; Genome; Chromosome; Molecular biology; Gene; Astrophysics; Physics","retraction":null,"screen_n_in":null,"score":{"opus":0.01993986655212406,"gpt":0.2186878056828029,"spread":0.1987479391306789,"validation_status":"score_only:v0-immature-baseline"},"prediction":{"model_version":"codex-gemma-dda1882f352a","candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0002532586,0.0001257799,0.0001438197,0.00004335571,0.00006627485,0.00001424255,0.00009160824,0.00007479064,0.00004676763],"category_scores_gemma":[0.0002676987,0.0001401272,0.00004688255,0.0001234951,0.00004243919,0.000003257786,0.00006919163,0.0000809796,0.000006394846],"about_ca_system_candidate":false,"about_ca_system_consensus":false,"about_ca_system_score_codex":0.00002183416,"about_ca_system_score_gemma":0.00004931554,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_topic_score_codex":0.0006616614,"about_ca_topic_score_gemma":0.0009858748,"domain_scores_codex":[0.9989839,0.0001087145,0.000304386,0.0002608266,0.00006584335,0.0002762813],"domain_scores_gemma":[0.999572,0.00006883962,0.00008159104,0.0001900906,0.00004735931,0.00004010273],"domain_codex":null,"domain_gemma":null,"domain_candidate":null,"domain_consensus":null,"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","study_design_scores_codex":[0.00003868309,0.00005444973,0.2970101,0.00002899951,0.00001785073,0.00001353716,0.0002644666,0.004324226,0.6711621,0.000002130475,0.000003089121,0.02708039],"study_design_scores_gemma":[0.0008988351,0.0003670967,0.7022671,0.0001162679,0.000018726,0.0001331894,0.0003820401,0.009070451,0.2862216,0.00004957335,0.0001782124,0.0002969097],"study_design_candidate":"observational","study_design_consensus":null,"genre_codex":"empirical","genre_gemma":"empirical","genre_scores_codex":[0.9979953,0.0001042388,0.0004405428,0.00001102514,0.00005311903,0.0001504932,0.00001227617,0.00001394056,0.001219128],"genre_scores_gemma":[0.9804942,0.000009151814,0.01917515,0.00002646754,0.0001292184,0.00001079777,0.00001329581,0.0000168749,0.0001248179],"genre_candidate":"empirical","genre_consensus":"empirical","teacher_disagreement_score":0.405257,"threshold_uncertainty_score":0.5714222,"prediction_status":"machine_predicted_unvalidated"},"labels":[],"label_agreement":null},{"id":"W1972754006","doi":"10.1089/109065701753145556","title":"Psychosocial Impact of C282Y Mutation Testing for Hemochromatosis","year":2001,"lang":"en","type":"article","venue":"Genetic Testing","topic":"Iron Metabolism and Disorders","field":"Medicine","cited_by":39,"is_retracted":false,"has_abstract":true,"routes":{"ca_aff":true,"ca_fund":true,"ca_venue":false,"about_ca":false},"ca_institutions":"Western University","funders":"Medical Research Council Canada","keywords":"Genetic testing; Anxiety; Psychosocial; Hemochromatosis; Medicine; Clinical psychology; Mental health; Psychiatry; Population; Genetic counseling; Psychology; Internal medicine; Genetics","retraction":null,"screen_n_in":null,"score":{"opus":0.04144171120278146,"gpt":0.3336590020913361,"spread":0.2922172908885546,"validation_status":"score_only:v0-immature-baseline"},"prediction":{"model_version":"codex-gemma-dda1882f352a","candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0001292267,0.0001162967,0.0002217985,0.00008024441,0.00008466881,0.00001019115,0.00005193479,0.00005593016,0.0000355076],"category_scores_gemma":[0.002018858,0.0001056293,0.0001013229,0.000393331,0.00003914355,0.00003049575,0.00001176027,0.00005247013,0.000005625167],"about_ca_system_candidate":false,"about_ca_system_consensus":false,"about_ca_system_score_codex":0.00002410805,"about_ca_system_score_gemma":0.0001416273,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_topic_score_codex":0.000214572,"about_ca_topic_score_gemma":0.000002963024,"domain_scores_codex":[0.9991146,0.00001583522,0.0002869922,0.0001784831,0.000147572,0.0002565394],"domain_scores_gemma":[0.9991247,0.0002896746,0.0001533517,0.0001416396,0.0002108435,0.00007980771],"domain_codex":null,"domain_gemma":null,"domain_candidate":null,"domain_consensus":null,"study_design_codex":"observational","study_design_gemma":"observational","study_design_scores_codex":[0.00007580517,0.0001124294,0.6652649,0.0001925545,0.00002237547,0.00000997248,0.0003720931,0.0004954532,0.0844235,0.00001123881,0.0004081026,0.2486116],"study_design_scores_gemma":[0.002034574,0.0005825275,0.9914681,0.0001020756,0.0001479854,0.0001676321,0.000146596,0.003440835,0.001100839,0.0006334027,0.00004329955,0.0001321669],"study_design_candidate":"observational","study_design_consensus":"observational","genre_codex":"empirical","genre_gemma":"empirical","genre_scores_codex":[0.9918181,0.0004030071,0.003743906,0.00006503257,0.0000962745,0.0003811285,0.000007196184,0.00006872377,0.003416661],"genre_scores_gemma":[0.8824814,0.000003483716,0.1171006,0.00006194736,0.0002511689,0.00001980575,0.00001009481,0.00002339517,0.00004812961],"genre_candidate":"empirical","genre_consensus":"empirical","teacher_disagreement_score":0.3262031,"threshold_uncertainty_score":0.4307438,"prediction_status":"machine_predicted_unvalidated"},"labels":[],"label_agreement":null},{"id":"W2070595851","doi":"10.1089/gte.2006.10.229","title":"Strategy for Comprehensive Molecular Testing for Duchenne and Becker Muscular Dystrophies","year":2006,"lang":"en","type":"article","venue":"Genetic Testing","topic":"Muscle Physiology and Disorders","field":"Biochemistry, Genetics and Molecular Biology","cited_by":36,"is_retracted":false,"has_abstract":true,"routes":{"ca_aff":true,"ca_fund":false,"ca_venue":false,"about_ca":false},"ca_institutions":"Hospital for Sick Children; University of Toronto","funders":"","keywords":"Gene duplication; Exon; Genetics; Duchenne muscular dystrophy; Gene; Multiplex ligation-dependent probe amplification; Genetic testing; Biology; Multiplex polymerase chain reaction; Muscular dystrophy; Coding region; Intron; Copy-number variation; genomic DNA; Polymerase chain reaction; Genome","retraction":null,"screen_n_in":null,"score":{"opus":0.03524289088913354,"gpt":0.2681217509781758,"spread":0.2328788600890423,"validation_status":"score_only:v0-immature-baseline"},"prediction":{"model_version":"codex-gemma-dda1882f352a","candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00007059959,0.0001975728,0.0001742032,0.00003303999,0.0001956948,0.00002656989,0.000100264,0.0001278166,0.000001187235],"category_scores_gemma":[0.000348271,0.0002049673,0.00007033091,0.00008165283,0.0001248123,0.000002795435,0.00006306967,0.00004997156,7.973242e-7],"about_ca_system_candidate":false,"about_ca_system_consensus":false,"about_ca_system_score_codex":0.000004652725,"about_ca_system_score_gemma":0.00005122628,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_topic_score_codex":0.00005920746,"about_ca_topic_score_gemma":0.00001254209,"domain_scores_codex":[0.9988836,0.00002851105,0.0002228194,0.0004489693,0.00005378047,0.0003623025],"domain_scores_gemma":[0.999271,0.000141849,0.00009959774,0.0002047308,0.0002295516,0.00005330186],"domain_codex":null,"domain_gemma":null,"domain_candidate":null,"domain_consensus":null,"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","study_design_scores_codex":[0.00004656385,0.00002959774,0.002955034,0.0001088591,0.00003350723,0.000002093088,0.000008520055,0.008539356,0.9800903,0.0001389148,0.0003315554,0.007715732],"study_design_scores_gemma":[0.01199564,0.008835881,0.441507,0.0002332318,0.0006163402,0.0002488947,0.0007673764,0.0511604,0.4246988,0.0425315,0.01415368,0.003251202],"study_design_candidate":"bench_or_experimental","study_design_consensus":null,"genre_codex":"empirical","genre_gemma":"empirical","genre_scores_codex":[0.9803756,0.002940001,0.0156983,0.00004811003,0.00005383113,0.0005400536,0.00002794548,0.00003791534,0.0002782589],"genre_scores_gemma":[0.9266435,0.000005661187,0.07261985,0.0001429537,0.0002473358,0.0001510676,0.0001103727,0.0000344592,0.00004482959],"genre_candidate":"empirical","genre_consensus":"empirical","teacher_disagreement_score":0.5553915,"threshold_uncertainty_score":0.8358323,"prediction_status":"machine_predicted_unvalidated"},"labels":[],"label_agreement":null},{"id":"W1998336357","doi":"10.1089/109065701750168644","title":"Decision Analysis of Prenatal Testing for Chromosomal Disorders: What Do the Preferences of Pregnant Women Tell Us?","year":2001,"lang":"en","type":"article","venue":"Genetic Testing","topic":"Prenatal Screening and Diagnostics","field":"Medicine","cited_by":27,"is_retracted":false,"has_abstract":true,"routes":{"ca_aff":true,"ca_fund":false,"ca_venue":false,"about_ca":false},"ca_institutions":"Institute of Health Economics","funders":"Eunice Kennedy Shriver National Institute of Child Health and Human Development; National Human Genome Research Institute; Agency for Healthcare Research and Quality; National Institutes of Health","keywords":"Miscarriage; Medicine; Preference; Guideline; Genetic testing; Test (biology); Obstetrics; Pregnancy; Internal medicine; Pathology; Statistics","retraction":null,"screen_n_in":null,"score":{"opus":0.03713781813130468,"gpt":0.2814303372158225,"spread":0.2442925190845178,"validation_status":"score_only:v0-immature-baseline"},"prediction":{"model_version":"codex-gemma-dda1882f352a","candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0003241598,0.0001546203,0.0003947707,0.0001505523,0.00009715812,0.00003469732,0.0002221692,0.00006759805,0.00003218303],"category_scores_gemma":[0.00729586,0.0001025063,0.0001096086,0.0011251,0.0001045827,0.00008991304,0.0001231358,0.00009508773,9.243277e-7],"about_ca_system_candidate":false,"about_ca_system_consensus":false,"about_ca_system_score_codex":0.00002500287,"about_ca_system_score_gemma":0.00008070787,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_topic_score_codex":0.0001455999,"about_ca_topic_score_gemma":0.00004877842,"domain_scores_codex":[0.9984968,0.00003530502,0.000516658,0.0002860196,0.0003303276,0.0003348603],"domain_scores_gemma":[0.995158,0.003788391,0.0003301358,0.0003795534,0.0002449648,0.00009900903],"domain_codex":null,"domain_gemma":null,"domain_candidate":null,"domain_consensus":null,"study_design_codex":"observational","study_design_gemma":"observational","study_design_scores_codex":[0.00006018885,0.00008724355,0.5691764,0.00009562781,0.0001614357,0.000002695921,0.0004643199,0.003903909,0.001234744,0.000002470556,0.000005084304,0.4248058],"study_design_scores_gemma":[0.0008625633,0.001459738,0.9398872,0.002563534,0.001096304,0.00002842786,0.001122958,0.04943356,0.002705771,0.0006209254,0.00005112537,0.0001678406],"study_design_candidate":"observational","study_design_consensus":"observational","genre_codex":"empirical","genre_gemma":"empirical","genre_scores_codex":[0.9919046,0.00378064,0.003373469,0.00002191063,0.00006784054,0.0004501502,0.00002586409,0.00003639307,0.0003391929],"genre_scores_gemma":[0.9597256,0.0002457397,0.03984374,0.00001184824,0.00007012243,0.00005322669,0.00001485418,0.00001522044,0.00001969061],"genre_candidate":"empirical","genre_consensus":"empirical","teacher_disagreement_score":0.424638,"threshold_uncertainty_score":0.8734353,"prediction_status":"machine_predicted_unvalidated"},"labels":[],"label_agreement":null},{"id":"W2093621196","doi":"10.1089/10906570152742290","title":"Spectrum of Mutations in the <i>CFTR</i> Gene of Patients with Classical and Atypical Forms of Cystic Fibrosis from Southwestern Sweden: Identification of 12 Novel Mutations","year":2001,"lang":"en","type":"article","venue":"Genetic Testing","topic":"Cystic Fibrosis Research Advances","field":"Medicine","cited_by":26,"is_retracted":false,"has_abstract":true,"routes":{"ca_aff":true,"ca_fund":false,"ca_venue":false,"about_ca":false},"ca_institutions":"Hospital for Sick Children","funders":"","keywords":"Cystic fibrosis; Mutation; Genetics; Allele; Genotype; Biology; Gene; ΔF508; Cystic fibrosis transmembrane conductance regulator; Phenotype; Population; Molecular biology; Medicine","retraction":null,"screen_n_in":null,"score":{"opus":0.02383899304387917,"gpt":0.27652479058853,"spread":0.2526857975446508,"validation_status":"score_only:v0-immature-baseline"},"prediction":{"model_version":"codex-gemma-dda1882f352a","candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0001538147,0.00009751908,0.0002749541,0.0001269983,0.00003257539,0.000007295889,0.0001109164,0.00003985325,0.000007636458],"category_scores_gemma":[0.001113019,0.00006849683,0.00003311102,0.0004400794,0.0003208627,0.00005406862,0.00003772094,0.00009635866,5.752332e-7],"about_ca_system_candidate":false,"about_ca_system_consensus":false,"about_ca_system_score_codex":0.00002005441,"about_ca_system_score_gemma":0.00008644207,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_topic_score_codex":0.0001135804,"about_ca_topic_score_gemma":0.0001768592,"domain_scores_codex":[0.9984959,0.00004159656,0.0006498215,0.0001873828,0.0004618674,0.0001634377],"domain_scores_gemma":[0.9980658,0.001064065,0.0003532807,0.0002541404,0.0002107848,0.0000518839],"domain_codex":null,"domain_gemma":null,"domain_candidate":null,"domain_consensus":null,"study_design_codex":"observational","study_design_gemma":"observational","study_design_scores_codex":[0.0002876127,0.0003308062,0.7289395,0.0001302062,0.00002393383,0.000001782939,0.0009210375,0.0007701113,0.2662014,0.00001893631,7.758463e-7,0.002373934],"study_design_scores_gemma":[0.001487772,0.0005549868,0.9801041,0.0002553455,0.0001021744,0.00001188262,0.0005061034,0.003094792,0.01332305,0.0005016692,0.000001744932,0.00005633152],"study_design_candidate":"observational","study_design_consensus":"observational","genre_codex":"empirical","genre_gemma":"empirical","genre_scores_codex":[0.985449,0.0001113112,0.01367224,0.00008211262,0.00001224995,0.0004462845,0.0001960292,0.000006072168,0.00002468989],"genre_scores_gemma":[0.960311,0.000003491527,0.03954324,0.000005474697,0.00001695358,0.00001931034,0.00008416606,0.00001167274,0.000004688403],"genre_candidate":"empirical","genre_consensus":"empirical","teacher_disagreement_score":0.2528784,"threshold_uncertainty_score":0.279322,"prediction_status":"machine_predicted_unvalidated"},"labels":[],"label_agreement":null},{"id":"W2003763230","doi":"10.1089/109065703322783635","title":"Heteroduplex-Based Genotyping with Microchip Electrophoresis and dHPLC","year":2003,"lang":"en","type":"article","venue":"Genetic Testing","topic":"Microfluidic and Capillary Electrophoresis Applications","field":"Engineering","cited_by":26,"is_retracted":false,"has_abstract":true,"routes":{"ca_aff":true,"ca_fund":false,"ca_venue":false,"about_ca":false},"ca_institutions":"University of Alberta","funders":"","keywords":"Heteroduplex; Electropherogram; Amplicon; Genotyping; Denaturing high performance liquid chromatography; Computational biology; Biology; Chromatography; Genetics; Mutation; DNA; Chemistry; Electrophoresis; Polymerase chain reaction; Gene; Genotype","retraction":null,"screen_n_in":null,"score":{"opus":0.007292235488634898,"gpt":0.1669143648846795,"spread":0.1596221293960446,"validation_status":"score_only:v0-immature-baseline"},"prediction":{"model_version":"codex-gemma-dda1882f352a","candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00008698108,0.0001727325,0.0001323536,0.00006258592,0.0001466285,0.00004383971,0.00008084677,0.00004801071,0.00002429491],"category_scores_gemma":[0.00004671834,0.0001658831,0.00001808748,0.000291695,0.00004069184,0.00001719407,0.000007113141,0.0001157763,0.00001074717],"about_ca_system_candidate":false,"about_ca_system_consensus":false,"about_ca_system_score_codex":0.00003470129,"about_ca_system_score_gemma":0.00004230806,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_topic_score_codex":0.00001042614,"about_ca_topic_score_gemma":0.000003837084,"domain_scores_codex":[0.9991013,0.00002327359,0.0001610717,0.0002426623,0.0001099813,0.0003616859],"domain_scores_gemma":[0.9995346,0.00007024757,0.00002621568,0.0002265147,0.0000570024,0.00008544117],"domain_codex":null,"domain_gemma":null,"domain_candidate":null,"domain_consensus":null,"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","study_design_scores_codex":[0.000003343452,0.000008022843,0.004112116,0.00004217084,0.00002023423,0.000004358433,0.00003922068,0.001073045,0.9888227,0.00009151491,0.001383653,0.00439961],"study_design_scores_gemma":[0.0008344266,0.0002530295,0.03675694,0.00008038301,0.0001069952,0.000296643,0.00005542768,0.007440247,0.9195386,0.0004461395,0.03330813,0.0008830818],"study_design_candidate":"bench_or_experimental","study_design_consensus":"bench_or_experimental","genre_codex":"empirical","genre_gemma":"empirical","genre_scores_codex":[0.9430472,0.0312353,0.02412761,0.00002748888,0.00001722913,0.0001641397,0.000002307704,0.0002127987,0.001165895],"genre_scores_gemma":[0.9746521,0.001039247,0.02406201,0.00008347637,0.00003368697,0.00004130244,0.000004089023,0.00005365949,0.0000303951],"genre_candidate":"empirical","genre_consensus":"empirical","teacher_disagreement_score":0.06928416,"threshold_uncertainty_score":0.6764516,"prediction_status":"machine_predicted_unvalidated"},"labels":[],"label_agreement":null},{"id":"W2059502776","doi":"10.1089/109065702760093906","title":"Health-Related Quality-of-Life Assessment of Prenatal Diagnosis: Chorionic Villi Sampling and Amniocentesis","year":2002,"lang":"en","type":"article","venue":"Genetic Testing","topic":"Prenatal Screening and Diagnostics","field":"Medicine","cited_by":25,"is_retracted":false,"has_abstract":true,"routes":{"ca_aff":true,"ca_fund":false,"ca_venue":false,"about_ca":true},"ca_institutions":"University of Toronto; McMaster University; Institute of Health Economics; University of Alberta","funders":"","keywords":"Amniocentesis; Chorionic villus sampling; Medicine; Obstetrics; Chorionic villi; Prenatal diagnosis; Pregnancy; Quality of life (healthcare); Gynecology; Randomized controlled trial; Surgery; Fetus","retraction":null,"screen_n_in":null,"score":{"opus":0.1234292104392263,"gpt":0.3533893061902437,"spread":0.2299600957510174,"validation_status":"score_only:v0-immature-baseline"},"prediction":{"model_version":"codex-gemma-dda1882f352a","candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0003960266,0.000144144,0.0005026063,0.00009014202,0.00008485309,0.000009847064,0.00007611138,0.00007309316,0.00005586577],"category_scores_gemma":[0.004589423,0.0001367362,0.0000575636,0.0002883176,0.0000894747,0.00003018049,0.00008953986,0.0001746918,0.000002141369],"about_ca_system_candidate":false,"about_ca_system_consensus":false,"about_ca_system_score_codex":0.00003959381,"about_ca_system_score_gemma":0.00009530499,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_topic_score_codex":0.001041575,"about_ca_topic_score_gemma":0.00001393672,"domain_scores_codex":[0.9982251,0.00009125483,0.0008365477,0.0002622614,0.0003062258,0.0002785881],"domain_scores_gemma":[0.9973598,0.00159238,0.0004400264,0.0002494844,0.0001183189,0.0002399991],"domain_codex":null,"domain_gemma":null,"domain_candidate":null,"domain_consensus":null,"study_design_codex":"observational","study_design_gemma":"observational","study_design_scores_codex":[0.000008022038,0.0001636727,0.9079552,0.0005699297,0.00005375658,0.000003786639,0.0001721302,0.0005890332,0.0002110796,0.00007192528,0.00004865058,0.09015286],"study_design_scores_gemma":[0.001238218,0.0004758352,0.9846563,0.001463419,0.00005619725,0.00003374166,0.00008573921,0.01146671,0.0003132281,0.00005831476,0.00002639693,0.0001259149],"study_design_candidate":"observational","study_design_consensus":"observational","genre_codex":"empirical","genre_gemma":"empirical","genre_scores_codex":[0.9824798,0.01470572,0.001352622,0.0004892066,0.00007250159,0.0002936903,0.00003195315,0.00006705034,0.0005074276],"genre_scores_gemma":[0.9359365,0.0004962158,0.06336135,0.00009411989,0.00004747224,0.00001970058,0.00001338983,0.00001862155,0.0000126243],"genre_candidate":"empirical","genre_consensus":"empirical","teacher_disagreement_score":0.09002694,"threshold_uncertainty_score":0.5575942,"prediction_status":"machine_predicted_unvalidated"},"labels":[],"label_agreement":null},{"id":"W1971760717","doi":"10.1089/gte.2007.0046","title":"<i>CFTR</i> Mutations in Turkish and North African Cystic Fibrosis Patients in Europe: Implications for Screening","year":2008,"lang":"en","type":"article","venue":"Genetic Testing","topic":"Cystic Fibrosis Research Advances","field":"Medicine","cited_by":22,"is_retracted":false,"has_abstract":true,"routes":{"ca_aff":true,"ca_fund":false,"ca_venue":false,"about_ca":false},"ca_institutions":"Hospital for Sick Children","funders":"","keywords":"Turkish; Cystic fibrosis; Allele; Mutation; Medicine; Turkish population; Internal medicine; Genetics; Gastroenterology; Pediatrics; Gene; Genotype; Biology","retraction":null,"screen_n_in":null,"score":{"opus":0.04573343926315311,"gpt":0.2946652220673102,"spread":0.2489317828041571,"validation_status":"score_only:v0-immature-baseline"},"prediction":{"model_version":"codex-gemma-dda1882f352a","candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00009646787,0.0001178466,0.0001967213,0.0001778284,0.0001435449,0.00001712245,0.00008026339,0.00002676909,0.000002464655],"category_scores_gemma":[0.005473662,0.000120761,0.00001864585,0.001146509,0.0001096083,0.00007252755,0.00006265456,0.0001331169,0.000002358378],"about_ca_system_candidate":false,"about_ca_system_consensus":false,"about_ca_system_score_codex":0.00005007093,"about_ca_system_score_gemma":0.0001194533,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_topic_score_codex":0.0002186963,"about_ca_topic_score_gemma":0.0002639313,"domain_scores_codex":[0.9987714,0.0000379539,0.000345222,0.0003188627,0.0001565631,0.0003700331],"domain_scores_gemma":[0.9983495,0.0009835887,0.00007285646,0.0001836844,0.0002675547,0.0001427707],"domain_codex":null,"domain_gemma":null,"domain_candidate":null,"domain_consensus":null,"study_design_codex":"observational","study_design_gemma":"observational","study_design_scores_codex":[0.00003283566,0.00007165309,0.9595584,0.00006253472,0.000003719349,0.00000816134,0.0002640338,0.001039572,0.002617954,0.000003535538,0.0000534629,0.03628419],"study_design_scores_gemma":[0.00133243,0.0002708793,0.9941381,0.0001466049,0.000013965,0.00004276619,0.00005310903,0.003418495,0.00005312643,0.00006037909,0.0003605403,0.0001096183],"study_design_candidate":"observational","study_design_consensus":"observational","genre_codex":"empirical","genre_gemma":"empirical","genre_scores_codex":[0.9956003,0.000307919,0.002713494,0.0002677606,0.00001490879,0.0008088571,0.00006714076,0.00003859653,0.0001809656],"genre_scores_gemma":[0.8041263,0.00001931334,0.1955004,0.00005697161,0.00003116083,0.0001581577,0.00006031496,0.00002200053,0.00002544555],"genre_candidate":"empirical","genre_consensus":"empirical","teacher_disagreement_score":0.1927869,"threshold_uncertainty_score":0.655288,"prediction_status":"machine_predicted_unvalidated"},"labels":[],"label_agreement":null},{"id":"W2093301275","doi":"10.1089/gte.2007.0108","title":"<i>BRCA1/2</i> in High-Risk African American Women with Breast Cancer: Providing Genetic Testing through Various Recruitment Strategies","year":2008,"lang":"en","type":"article","venue":"Genetic Testing","topic":"BRCA gene mutations in cancer","field":"Biochemistry, Genetics and Molecular Biology","cited_by":21,"is_retracted":false,"has_abstract":true,"routes":{"ca_aff":true,"ca_fund":false,"ca_venue":false,"about_ca":false},"ca_institutions":"Women's College Hospital","funders":"Moffitt Cancer Center","keywords":"Breast cancer; Medicine; Family history; Genetic counseling; Genetic testing; Cancer; Referral; Population; Oncology; Family medicine; Internal medicine; Genetics; Biology; Environmental health","retraction":null,"screen_n_in":null,"score":{"opus":0.03341835848145587,"gpt":0.2688424012611892,"spread":0.2354240427797334,"validation_status":"score_only:v0-immature-baseline"},"prediction":{"model_version":"codex-gemma-dda1882f352a","candidate_categories":["metaepi_narrow"],"consensus_categories":[],"category_scores_codex":[0.0001840535,0.0004209437,0.0003716945,0.00009634808,0.0003677146,0.00007793181,0.0003802511,0.0001014826,0.000009644028],"category_scores_gemma":[0.0001909788,0.0004050041,0.00003532902,0.001050938,0.000400629,0.00001678195,0.0001818467,0.0002662227,0.000004542155],"about_ca_system_candidate":false,"about_ca_system_consensus":false,"about_ca_system_score_codex":0.0004820593,"about_ca_system_score_gemma":0.00135509,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_topic_score_codex":0.006245635,"about_ca_topic_score_gemma":0.001300046,"domain_scores_codex":[0.9971569,0.0001621814,0.0005172192,0.0009445149,0.0003187955,0.0009004594],"domain_scores_gemma":[0.9984344,0.0001236753,0.0004598384,0.0005903624,0.0002481019,0.0001435746],"domain_codex":null,"domain_gemma":null,"domain_candidate":null,"domain_consensus":null,"study_design_codex":"observational","study_design_gemma":"observational","study_design_scores_codex":[0.0001497615,0.0001467836,0.616327,0.00006429486,0.0001529329,0.0001283978,0.003631819,0.1309218,0.09835874,0.000003130406,0.0001501263,0.1499652],"study_design_scores_gemma":[0.001637159,0.001624226,0.9780213,0.0001556433,0.00007871797,0.001065167,0.003878871,0.001344198,0.009549764,0.0002433065,0.001375486,0.001026165],"study_design_candidate":"observational","study_design_consensus":"observational","genre_codex":"empirical","genre_gemma":"empirical","genre_scores_codex":[0.9944735,0.000959914,0.00273267,0.0001139269,0.000127651,0.0007640866,0.00007093015,0.00008666186,0.0006707316],"genre_scores_gemma":[0.8607097,0.0002494752,0.1373115,0.0001656315,0.0004593775,0.0009620975,0.00001229699,0.00008935938,0.00004053774],"genre_candidate":"empirical","genre_consensus":"empirical","teacher_disagreement_score":0.3616942,"threshold_uncertainty_score":0.9998402,"prediction_status":"machine_predicted_unvalidated"},"labels":[],"label_agreement":null},{"id":"W2090566866","doi":"10.1089/10906570152742326","title":"Rapid Detection of the Sacsin Mutations Causing Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay","year":2001,"lang":"en","type":"article","venue":"Genetic Testing","topic":"Genetic Neurodegenerative Diseases","field":"Neuroscience","cited_by":20,"is_retracted":false,"has_abstract":true,"routes":{"ca_aff":true,"ca_fund":true,"ca_venue":false,"about_ca":true},"ca_institutions":"Hôpital de l'Enfant-Jésus; McGill Genome Centre; McGill University Health Centre; Université de Montréal; Cégep de Chicoutimi; Centre Hospitalier Universitaire Sainte-Justine","funders":"Medical Research Council Canada","keywords":"Genetics; Nonsense mutation; Allele; Mutation; Exon; Spinocerebellar ataxia; Biology; Ataxia; Gene; Missense mutation; Neuroscience","retraction":null,"screen_n_in":null,"score":{"opus":0.0494004826091981,"gpt":0.2637361885035098,"spread":0.2143357058943117,"validation_status":"score_only:v0-immature-baseline"},"prediction":{"model_version":"codex-gemma-dda1882f352a","candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00008367211,0.0001669487,0.0001781716,0.0001019811,0.0002657007,0.00002488862,0.0002407604,0.00003979272,0.00002585653],"category_scores_gemma":[0.005065938,0.0001407615,0.0000760895,0.000929758,0.0002766364,0.00006056016,0.0001159291,0.0001175867,0.000006257022],"about_ca_system_candidate":false,"about_ca_system_consensus":false,"about_ca_system_score_codex":0.00002566748,"about_ca_system_score_gemma":0.0001247527,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_topic_score_codex":0.00006946871,"about_ca_topic_score_gemma":0.00003699408,"domain_scores_codex":[0.9982468,0.0002982674,0.000428678,0.0003903825,0.0003566759,0.0002791184],"domain_scores_gemma":[0.9982836,0.00064088,0.0004422633,0.000387042,0.0001774823,0.00006877706],"domain_codex":null,"domain_gemma":null,"domain_candidate":null,"domain_consensus":null,"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","study_design_scores_codex":[0.000007772982,0.00004431947,0.01265315,0.00002521351,0.000003079204,0.000007542947,0.0001709283,0.01084401,0.960867,0.000005025938,0.000006329049,0.01536558],"study_design_scores_gemma":[0.0001946944,0.00007713835,0.2134854,0.00006664118,0.00004014151,0.00008114152,0.00005124773,0.01043409,0.7753305,0.0001213088,0.00001571237,0.0001019719],"study_design_candidate":"bench_or_experimental","study_design_consensus":"bench_or_experimental","genre_codex":"empirical","genre_gemma":"empirical","genre_scores_codex":[0.9950699,0.0001707613,0.003639719,0.0000655636,0.000300627,0.0003249541,0.00002586221,0.00005716505,0.0003454163],"genre_scores_gemma":[0.9984475,0.00001081989,0.001260776,0.00007706892,0.00008207621,0.00002057222,7.638697e-7,0.00002634837,0.00007412054],"genre_candidate":"empirical","genre_consensus":"empirical","teacher_disagreement_score":0.2008322,"threshold_uncertainty_score":0.6064767,"prediction_status":"machine_predicted_unvalidated"},"labels":[],"label_agreement":null},{"id":"W1965861571","doi":"10.1089/gte.2007.0119","title":"Three New <i>BLM</i> Gene Mutations Associated with Bloom Syndrome","year":2008,"lang":"en","type":"article","venue":"Genetic Testing","topic":"DNA Repair Mechanisms","field":"Biochemistry, Genetics and Molecular Biology","cited_by":19,"is_retracted":false,"has_abstract":true,"routes":{"ca_aff":false,"ca_fund":true,"ca_venue":false,"about_ca":false},"ca_institutions":"","funders":"Institute of Cancer Research; U.S. Bureau of Land Management; Institut National Du Cancer","keywords":"Frameshift mutation; Bloom syndrome; Genetics; Nonsense mutation; Gene; Mutation; Biology; Gene mutation; Nonsense; Population; Medicine; Missense mutation","retraction":null,"screen_n_in":null,"score":{"opus":0.02307981821716076,"gpt":0.2128460918151156,"spread":0.1897662735979549,"validation_status":"score_only:v0-immature-baseline"},"prediction":{"model_version":"codex-gemma-dda1882f352a","candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00008182337,0.0001880671,0.0001502685,0.0000363153,0.0001914246,0.00001760945,0.0001908051,0.0001184668,0.00002152783],"category_scores_gemma":[0.0003929955,0.0001828746,0.00004966043,0.0002372551,0.00006896156,0.000002316541,0.00008442834,0.00008605462,0.00002180281],"about_ca_system_candidate":false,"about_ca_system_consensus":false,"about_ca_system_score_codex":0.00001814032,"about_ca_system_score_gemma":0.0002663033,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_topic_score_codex":0.00007516961,"about_ca_topic_score_gemma":0.0001138894,"domain_scores_codex":[0.9988211,0.00002511185,0.0002068953,0.00040193,0.0001958152,0.0003491578],"domain_scores_gemma":[0.9992089,0.00003884612,0.0001201841,0.0003707662,0.0001131764,0.000148162],"domain_codex":null,"domain_gemma":null,"domain_candidate":null,"domain_consensus":null,"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","study_design_scores_codex":[0.00001273896,0.00007263201,0.06396572,0.000005837902,0.0001372156,0.0003080851,0.00008507254,0.001939289,0.9296064,0.00001143328,0.0007645072,0.003091103],"study_design_scores_gemma":[0.002915314,0.002346187,0.5037944,0.0001222979,0.0002183816,0.006943483,0.00005142517,0.001952457,0.4784873,0.001328166,0.0006166902,0.001223896],"study_design_candidate":"bench_or_experimental","study_design_consensus":null,"genre_codex":"empirical","genre_gemma":"empirical","genre_scores_codex":[0.9808758,0.0004074055,0.01764197,0.00003487553,0.00007208393,0.0002052269,0.00001151392,0.00008716409,0.0006639406],"genre_scores_gemma":[0.9092456,0.000006748888,0.08968247,0.0001515705,0.0001112099,0.00001337005,0.00007767044,0.00004523076,0.0006661132],"genre_candidate":"empirical","genre_consensus":"empirical","teacher_disagreement_score":0.451119,"threshold_uncertainty_score":0.7457411,"prediction_status":"machine_predicted_unvalidated"},"labels":[],"label_agreement":null},{"id":"W1999936743","doi":"10.1089/gte.2006.10.60","title":"Genetic Testing for Huntington's Disease: How Is the Decision Taken?","year":2006,"lang":"en","type":"article","venue":"Genetic Testing","topic":"Genetic Neurodegenerative Diseases","field":"Neuroscience","cited_by":19,"is_retracted":false,"has_abstract":true,"routes":{"ca_aff":true,"ca_fund":false,"ca_venue":false,"about_ca":false},"ca_institutions":"Institute of Population and Public Health","funders":"","keywords":"Test (biology); Genetic testing; Psychology; Predictive testing; Disease; Decision analysis; Genetic counseling; Genetic discrimination; Social psychology; Applied psychology; Cognitive psychology; Actuarial science; Medicine; Genetics; Business; Biology; Economics","retraction":null,"screen_n_in":null,"score":{"opus":0.05038063457942717,"gpt":0.2687380322385161,"spread":0.2183573976590889,"validation_status":"score_only:v0-immature-baseline"},"prediction":{"model_version":"codex-gemma-dda1882f352a","candidate_categories":["metaresearch","metaepi_narrow"],"consensus_categories":[],"category_scores_codex":[0.0001930205,0.0004412351,0.0002603318,0.0001134652,0.00109747,0.0004883198,0.0008260925,0.00005978142,0.00002835462],"category_scores_gemma":[0.01442918,0.0003562454,0.0001650316,0.0008905319,0.0002527079,0.00008710101,0.0002675955,0.0001693337,0.00004405495],"about_ca_system_candidate":false,"about_ca_system_consensus":false,"about_ca_system_score_codex":0.00004024999,"about_ca_system_score_gemma":0.0002053772,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_topic_score_codex":0.00003739577,"about_ca_topic_score_gemma":0.000008801107,"domain_scores_codex":[0.9964819,0.0001965004,0.0004936852,0.001230613,0.0006884526,0.0009088609],"domain_scores_gemma":[0.9934276,0.00477952,0.0003443956,0.0009037383,0.0003068966,0.0002378922],"domain_codex":null,"domain_gemma":null,"domain_candidate":null,"domain_consensus":null,"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","study_design_scores_codex":[0.00003025668,0.0001398008,0.1358702,0.00007806423,0.000005203416,0.00002834604,0.00007505749,0.01294224,0.6941161,0.0000897258,0.004239053,0.152386],"study_design_scores_gemma":[0.0007098572,0.0001863374,0.7043002,0.0001402101,0.0001234307,0.00002999593,0.00003851091,0.03964227,0.2466272,0.005553388,0.002024396,0.0006242186],"study_design_candidate":"bench_or_experimental","study_design_consensus":null,"genre_codex":"empirical","genre_gemma":"empirical","genre_scores_codex":[0.9872976,0.0006935588,0.008630916,0.0009460655,0.0003948675,0.001241644,0.0001015734,0.000249751,0.0004440329],"genre_scores_gemma":[0.9240171,0.000004952003,0.07298035,0.00140989,0.0007796856,0.0002613095,0.000003118924,0.0001056377,0.0004379707],"genre_candidate":"empirical","genre_consensus":"empirical","teacher_disagreement_score":0.5684301,"threshold_uncertainty_score":0.999889,"prediction_status":"machine_predicted_unvalidated"},"labels":[],"label_agreement":null},{"id":"W2174778765","doi":"10.1089/109065701753617444","title":"A Primer for Predicting Risk of Disease in <i>HFE</i> -Linked Hemochromatosis","year":2001,"lang":"en","type":"article","venue":"Genetic Testing","topic":"Iron Metabolism and Disorders","field":"Medicine","cited_by":18,"is_retracted":false,"has_abstract":true,"routes":{"ca_aff":true,"ca_fund":false,"ca_venue":false,"about_ca":false},"ca_institutions":"Western University","funders":"","keywords":"Hemochromatosis; Hereditary hemochromatosis; Penetrance; Proband; Genetics; Genotype; Allele; Genetic counseling; Population; Genetic testing; Compound heterozygosity; Heterozygote advantage; Medicine; Asymptomatic; Mutation; Biology; Internal medicine; Gene; Phenotype; Environmental health","retraction":null,"screen_n_in":null,"score":{"opus":0.02082149682298788,"gpt":0.2625133267360754,"spread":0.2416918299130875,"validation_status":"score_only:v0-immature-baseline"},"prediction":{"model_version":"codex-gemma-dda1882f352a","candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.000205345,0.0001147761,0.0002387729,0.00009128676,0.00005153735,0.000005607641,0.00006376936,0.00004261681,0.00001848813],"category_scores_gemma":[0.002257517,0.0001080473,0.00006872939,0.0003016698,0.00004336488,0.00002541047,0.00002926034,0.00008320824,0.000003017073],"about_ca_system_candidate":false,"about_ca_system_consensus":false,"about_ca_system_score_codex":0.00001211394,"about_ca_system_score_gemma":0.0001125838,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_topic_score_codex":0.0002195734,"about_ca_topic_score_gemma":0.000008838661,"domain_scores_codex":[0.9989635,0.00003039029,0.0003501901,0.0002249851,0.0001565215,0.0002744577],"domain_scores_gemma":[0.9991534,0.0002650365,0.0001431617,0.0002279155,0.00007877714,0.0001317342],"domain_codex":null,"domain_gemma":null,"domain_candidate":null,"domain_consensus":null,"study_design_codex":"observational","study_design_gemma":"observational","study_design_scores_codex":[0.000126733,0.0001075747,0.9703472,0.0002234824,0.000007471103,0.000008082583,0.0001923387,0.0004558334,0.005232034,0.000005543018,0.00004640458,0.02324732],"study_design_scores_gemma":[0.002558073,0.000110685,0.9870341,0.0001909796,0.0002481476,0.000009736873,0.0001226148,0.00855402,0.0005679476,0.0002552829,0.0002365481,0.0001119108],"study_design_candidate":"observational","study_design_consensus":"observational","genre_codex":"empirical","genre_gemma":"empirical","genre_scores_codex":[0.9949756,0.001720822,0.001830238,0.0001099603,0.00007568162,0.0005758274,0.00001477923,0.00005505054,0.0006420585],"genre_scores_gemma":[0.9525753,0.00006806903,0.04696558,0.0001160465,0.0001171637,0.00004831722,0.000008353432,0.00002496164,0.00007622523],"genre_candidate":"empirical","genre_consensus":"empirical","teacher_disagreement_score":0.04513534,"threshold_uncertainty_score":0.4406041,"prediction_status":"machine_predicted_unvalidated"},"labels":[],"label_agreement":null},{"id":"W2042573312","doi":"10.1089/gte.2008.0013","title":"Ethnic Differences in the Frequency of the Cardioprotective C679X PCSK9 Mutation in a West African Population","year":2008,"lang":"en","type":"article","venue":"Genetic Testing","topic":"Lipoproteins and Cardiovascular Health","field":"Medicine","cited_by":18,"is_retracted":false,"has_abstract":true,"routes":{"ca_aff":true,"ca_fund":false,"ca_venue":false,"about_ca":false},"ca_institutions":"Université de Montréal; Ottawa Hospital","funders":"","keywords":"PCSK9; Allele frequency; Mutation; Ethnic group; Population; Genetics; Loss of heterozygosity; Biology; Apolipoprotein B; Internal medicine; Allele; LDL receptor; Endocrinology; Gene; Cholesterol; Medicine; Lipoprotein; Environmental health","retraction":null,"screen_n_in":null,"score":{"opus":0.06216401517141777,"gpt":0.2709225270542495,"spread":0.2087585118828317,"validation_status":"score_only:v0-immature-baseline"},"prediction":{"model_version":"codex-gemma-dda1882f352a","candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0005408634,0.00008419749,0.0002227823,0.0000721812,0.00007729777,0.000003542358,0.00009835474,0.00005152206,0.000002930432],"category_scores_gemma":[0.0006720321,0.00004921815,0.00007987098,0.000773733,0.00005657762,0.00002123389,0.00001907289,0.000218996,9.878047e-7],"about_ca_system_candidate":false,"about_ca_system_consensus":false,"about_ca_system_score_codex":0.00007543238,"about_ca_system_score_gemma":0.0001163347,"about_ca_topic_candidate":true,"about_ca_topic_consensus":false,"about_ca_topic_score_codex":0.01679152,"about_ca_topic_score_gemma":0.001160169,"domain_scores_codex":[0.9987433,0.0002705339,0.000280594,0.0001639341,0.0003752274,0.0001664141],"domain_scores_gemma":[0.9993906,0.0001079065,0.000109118,0.0003100017,0.00006000161,0.00002239191],"domain_codex":null,"domain_gemma":null,"domain_candidate":null,"domain_consensus":null,"study_design_codex":"observational","study_design_gemma":"observational","study_design_scores_codex":[0.000005405734,0.00003261116,0.9377214,0.00005805528,0.00001212674,0.00003099231,0.004258252,0.0002156078,0.0008933824,0.00001278531,4.016492e-7,0.05675902],"study_design_scores_gemma":[0.0004142254,0.00009549194,0.9972281,0.0001572026,0.0000243195,0.0002223509,0.0007994267,0.0003992205,0.0001531893,0.0004541203,9.985824e-7,0.00005134854],"study_design_candidate":"observational","study_design_consensus":"observational","genre_codex":"empirical","genre_gemma":"empirical","genre_scores_codex":[0.9969874,0.001086935,0.0001531573,0.0001860337,0.00004350749,0.0008780878,0.000001461873,0.00001148506,0.0006519119],"genre_scores_gemma":[0.998311,0.00001370377,0.001427866,0.00004981787,0.00009395682,0.00008895084,0.000001612321,0.000008078478,0.000005023017],"genre_candidate":"empirical","genre_consensus":"empirical","teacher_disagreement_score":0.05950675,"threshold_uncertainty_score":0.9897557,"prediction_status":"machine_predicted_unvalidated"},"labels":[],"label_agreement":null},{"id":"W1985385175","doi":"10.1089/gte.2006.0512","title":"Psychosocial Impact of Genetic Testing for Hemochromatosis in The HEIRS Study: A Comparison of Participants Recruited in Canada And in The United States","year":2007,"lang":"en","type":"article","venue":"Genetic Testing","topic":"Iron Metabolism and Disorders","field":"Medicine","cited_by":18,"is_retracted":false,"has_abstract":true,"routes":{"ca_aff":true,"ca_fund":false,"ca_venue":false,"about_ca":true},"ca_institutions":"London Health Sciences Centre","funders":"National Center for Research Resources; National Heart, Lung, and Blood Institute","keywords":"Hemochromatosis; Worry; Psychosocial; Genetic testing; Medicine; Mental health; Hereditary hemochromatosis; Population; Psychiatry; Clinical psychology; Environmental health; Internal medicine; Anxiety","retraction":null,"screen_n_in":null,"score":{"opus":0.1030123434751969,"gpt":0.3768990073639099,"spread":0.273886663888713,"validation_status":"score_only:v0-immature-baseline"},"prediction":{"model_version":"codex-gemma-dda1882f352a","candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.001071533,0.0001424056,0.0003902267,0.0002057951,0.00004659565,0.000008906679,0.0001452298,0.0000359999,0.000002006366],"category_scores_gemma":[0.001844241,0.00009390096,0.00002586509,0.001410945,0.00006319267,0.00001313088,0.00002121365,0.0001520255,5.385818e-8],"about_ca_system_candidate":false,"about_ca_system_consensus":false,"about_ca_system_score_codex":0.00006626882,"about_ca_system_score_gemma":0.0003821925,"about_ca_topic_candidate":true,"about_ca_topic_consensus":true,"about_ca_topic_score_codex":0.7188881,"about_ca_topic_score_gemma":0.6791675,"domain_scores_codex":[0.9981824,0.0001859283,0.0007433863,0.0001844869,0.000270323,0.0004334702],"domain_scores_gemma":[0.9973651,0.002072198,0.0002263597,0.0002009268,0.00008548349,0.00004997432],"domain_codex":null,"domain_gemma":null,"domain_candidate":null,"domain_consensus":null,"study_design_codex":"observational","study_design_gemma":"observational","study_design_scores_codex":[0.00009938327,0.0002754586,0.9717206,0.00009922066,0.000008962051,0.00001242533,0.01294447,0.002819066,0.001031739,3.801193e-7,0.00002489822,0.01096343],"study_design_scores_gemma":[0.002276302,0.0004401597,0.9579471,0.000135523,0.00006075265,0.000006873727,0.03083213,0.008080876,0.00008472551,0.00004939221,0.000002007983,0.00008417796],"study_design_candidate":"observational","study_design_consensus":"observational","genre_codex":"empirical","genre_gemma":"empirical","genre_scores_codex":[0.9980264,0.0005926694,0.00003559817,0.00006457805,0.00002547378,0.001206151,0.000009491901,0.000005034115,0.00003459572],"genre_scores_gemma":[0.9970273,0.000005859459,0.002776455,0.0001064751,0.00002196723,0.00004106233,0.000006754623,0.00001365546,4.387394e-7],"genre_candidate":"empirical","genre_consensus":"empirical","teacher_disagreement_score":0.03972056,"threshold_uncertainty_score":0.382917,"prediction_status":"machine_predicted_unvalidated"},"labels":[],"label_agreement":null},{"id":"W2028587845","doi":"10.1089/gte.2004.8.139","title":"Subjective and Objective Risk of Breast Cancer in Ashkenazi Jewish Individuals at Risk for BRCA1/2 Mutations","year":2004,"lang":"en","type":"article","venue":"Genetic Testing","topic":"BRCA gene mutations in cancer","field":"Biochemistry, Genetics and Molecular Biology","cited_by":14,"is_retracted":false,"has_abstract":true,"routes":{"ca_aff":true,"ca_fund":false,"ca_venue":false,"about_ca":false},"ca_institutions":"Institute of Aging","funders":"","keywords":"Genetic counseling; Breast cancer; Family history; Medicine; Cancer; Genetic testing; Demography; Risk assessment; Oncology; Clinical psychology; Gynecology; Family medicine; Internal medicine; Genetics","retraction":null,"screen_n_in":null,"score":{"opus":0.01153716961039078,"gpt":0.2693579559653793,"spread":0.2578207863549885,"validation_status":"score_only:v0-immature-baseline"},"prediction":{"model_version":"codex-gemma-dda1882f352a","candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0002301777,0.0001572902,0.0001704779,0.00008806332,0.0001565433,0.00001433291,0.0001081307,0.000118101,0.00000722374],"category_scores_gemma":[0.0006756122,0.0001699742,0.00004948606,0.0002625641,0.0001510271,0.000004998566,0.0001089091,0.00009829476,9.192721e-7],"about_ca_system_candidate":false,"about_ca_system_consensus":false,"about_ca_system_score_codex":0.0001806433,"about_ca_system_score_gemma":0.0003627109,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_topic_score_codex":0.0008344946,"about_ca_topic_score_gemma":0.001998691,"domain_scores_codex":[0.9988532,0.00007049836,0.0002880272,0.0004283816,0.0001060796,0.0002538345],"domain_scores_gemma":[0.9990562,0.0001550197,0.0002848722,0.0002048809,0.0002445444,0.00005447965],"domain_codex":null,"domain_gemma":null,"domain_candidate":null,"domain_consensus":null,"study_design_codex":"observational","study_design_gemma":"observational","study_design_scores_codex":[0.00003292227,0.00004291259,0.8640405,0.00002739865,0.0001172213,7.564003e-7,0.0009026655,0.04571456,0.05685104,0.000007032042,0.00001872723,0.03224427],"study_design_scores_gemma":[0.001481333,0.0001576903,0.9362863,0.00004937538,0.0001016778,0.0000348947,0.0002541426,0.0002634361,0.0585741,0.00256002,0.00004450771,0.0001924925],"study_design_candidate":"observational","study_design_consensus":"observational","genre_codex":"empirical","genre_gemma":"empirical","genre_scores_codex":[0.992424,0.002327071,0.002874813,0.0000534437,0.00009086498,0.0005076215,0.001589946,0.00001125196,0.0001210425],"genre_scores_gemma":[0.9734342,0.0001973399,0.02586669,0.00003000385,0.0001266676,0.000256127,0.00003337803,0.00003069908,0.00002486531],"genre_candidate":"empirical","genre_consensus":"empirical","teacher_disagreement_score":0.07224583,"threshold_uncertainty_score":0.6931347,"prediction_status":"machine_predicted_unvalidated"},"labels":[],"label_agreement":null},{"id":"W1974171154","doi":"10.1089/gte.2005.9.66","title":"Risk Assessment for Inherited Susceptibility to Cancer: A Review of the Psychosocial and Ethical Dimensions","year":2005,"lang":"en","type":"review","venue":"Genetic Testing","topic":"BRCA gene mutations in cancer","field":"Biochemistry, Genetics and Molecular Biology","cited_by":14,"is_retracted":false,"has_abstract":true,"routes":{"ca_aff":true,"ca_fund":false,"ca_venue":false,"about_ca":false},"ca_institutions":"Alberta Cancer Foundation; University of Calgary; Alberta Health; Institute of Health Economics; South Health Campus; Alberta Health Services","funders":"","keywords":"Psychosocial; Risk assessment; Ethical issues; German; Quality (philosophy); Psychology; Engineering ethics; Computer science; Engineering; Psychiatry","retraction":null,"screen_n_in":null,"score":{"opus":0.06127424562899281,"gpt":0.428015860990545,"spread":0.3667416153615522,"validation_status":"score_only:v0-immature-baseline"},"prediction":{"model_version":"codex-gemma-dda1882f352a","candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0006145465,0.0002615417,0.0006559278,0.00002827347,0.0001658444,0.0000135171,0.0002947451,0.0003818226,0.00001183778],"category_scores_gemma":[0.001951689,0.0001970097,0.0002628654,0.0003188103,0.0001168668,6.218302e-7,0.0002685146,0.0003743101,6.314685e-7],"about_ca_system_candidate":false,"about_ca_system_consensus":false,"about_ca_system_score_codex":0.00012236,"about_ca_system_score_gemma":0.001192879,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_topic_score_codex":0.00003897429,"about_ca_topic_score_gemma":0.0001086291,"domain_scores_codex":[0.9980696,0.000324138,0.0006391861,0.0005679176,0.0001702792,0.0002288367],"domain_scores_gemma":[0.9983026,0.0002147172,0.0004908866,0.000602663,0.0003094579,0.00007969656],"domain_codex":null,"domain_gemma":null,"domain_candidate":null,"domain_consensus":null,"study_design_codex":"design_other","study_design_gemma":"not_applicable","study_design_scores_codex":[0.000001823515,0.00001473884,0.0002398293,0.01149559,0.00007647152,6.726906e-8,0.00001416892,0.00001687108,0.0002067319,0.000002684913,0.002985865,0.9849452],"study_design_scores_gemma":[0.000140233,0.0001111287,0.001051296,0.02069536,0.0008000074,0.00001054987,0.000004423698,0.00001657453,0.0000200221,0.00003158952,0.9768724,0.0002464587],"study_design_candidate":"design_other","study_design_consensus":null,"genre_codex":"review","genre_gemma":"review","genre_scores_codex":[0.0004596458,0.995756,0.000503973,0.0004995581,0.0002623065,0.002067667,0.0003891871,0.000008474836,0.00005319577],"genre_scores_gemma":[0.0001177853,0.9479617,0.04977451,0.0007632865,0.0004719509,0.0008022309,0.00003594341,0.00004321096,0.0000294092],"genre_candidate":"review","genre_consensus":"review","teacher_disagreement_score":0.9846987,"threshold_uncertainty_score":0.8033821,"prediction_status":"machine_predicted_unvalidated"},"labels":[],"label_agreement":null},{"id":"W2019834541","doi":"10.1089/gte.2008.0035","title":"Development and Pilot Testing of a Decision Aid for Men Considering Genetic Testing for Breast and/or Ovarian Cancer–Related Mutations ( <i>BRCA1/2</i> )","year":2008,"lang":"en","type":"article","venue":"Genetic Testing","topic":"BRCA gene mutations in cancer","field":"Biochemistry, Genetics and Molecular Biology","cited_by":13,"is_retracted":false,"has_abstract":true,"routes":{"ca_aff":false,"ca_fund":true,"ca_venue":false,"about_ca":false},"ca_institutions":"","funders":"Goddard Space Flight Center; Cancer Research Society","keywords":"Genetic testing; Genetic counseling; Breast cancer; Family history; Ovarian cancer; Medicine; Gynecology; Family medicine; Cancer; Internal medicine; Biology; Genetics","retraction":null,"screen_n_in":null,"score":{"opus":0.0553028425818698,"gpt":0.2870817516422007,"spread":0.2317789090603309,"validation_status":"score_only:v0-immature-baseline"},"prediction":{"model_version":"codex-gemma-dda1882f352a","candidate_categories":["metaepi_narrow"],"consensus_categories":[],"category_scores_codex":[0.0002472904,0.0002584347,0.0002624401,0.0000955392,0.0005388681,0.0000321253,0.0001360282,0.0001104861,0.000003320617],"category_scores_gemma":[0.002097711,0.0002646313,0.00003151518,0.0003203632,0.0001514064,0.000008114918,0.0001529379,0.00007415836,3.544175e-7],"about_ca_system_candidate":false,"about_ca_system_consensus":false,"about_ca_system_score_codex":0.00006726974,"about_ca_system_score_gemma":0.000935706,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_topic_score_codex":0.00007785168,"about_ca_topic_score_gemma":0.00006683963,"domain_scores_codex":[0.9981736,0.00002871232,0.0006586096,0.0005988118,0.0001424023,0.0003978667],"domain_scores_gemma":[0.9979729,0.000874309,0.0003174265,0.0002315719,0.0004827633,0.0001210286],"domain_codex":null,"domain_gemma":null,"domain_candidate":null,"domain_consensus":null,"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","study_design_scores_codex":[0.0001370716,0.00007629695,0.09236824,0.0002838274,0.0001590916,0.0000105645,0.000903192,0.008191716,0.5017141,0.000006240001,0.00009201926,0.3960577],"study_design_scores_gemma":[0.01529762,0.003524751,0.588524,0.001606908,0.0006380566,0.008076401,0.001098252,0.1352988,0.237317,0.001558708,0.004696512,0.002362941],"study_design_candidate":"bench_or_experimental","study_design_consensus":null,"genre_codex":"empirical","genre_gemma":"methods","genre_scores_codex":[0.9723411,0.001548202,0.02477307,0.0000454205,0.0000982045,0.0009346337,0.0000852939,0.00005205071,0.0001219964],"genre_scores_gemma":[0.481306,0.00001684041,0.5182312,0.00003344722,0.00007936802,0.0002607695,0.00001155341,0.00003765542,0.00002319574],"genre_candidate":"empirical","genre_consensus":null,"teacher_disagreement_score":0.4961558,"threshold_uncertainty_score":0.9999806,"prediction_status":"machine_predicted_unvalidated"},"labels":[],"label_agreement":null},{"id":"W2084734987","doi":"10.1089/gte.2006.10.1","title":"A Fluorescent Multiplex-DGGE Screening Test for Mutations in the BRCA1 Gene","year":2006,"lang":"en","type":"article","venue":"Genetic Testing","topic":"BRCA gene mutations in cancer","field":"Biochemistry, Genetics and Molecular Biology","cited_by":12,"is_retracted":false,"has_abstract":true,"routes":{"ca_aff":true,"ca_fund":true,"ca_venue":false,"about_ca":false},"ca_institutions":"Coalition for Research in Women's Health; University of Toronto","funders":"Hospital for Sick Children","keywords":"Amplicon; Biology; Temperature gradient gel electrophoresis; Exon; Multiplex; Molecular biology; Genetics; Gene; Locus (genetics); Multiplex polymerase chain reaction; Polymerase chain reaction; Gene mutation; Mutation","retraction":null,"screen_n_in":null,"score":{"opus":0.02700855395164013,"gpt":0.276038135661652,"spread":0.2490295817100119,"validation_status":"score_only:v0-immature-baseline"},"prediction":{"model_version":"codex-gemma-dda1882f352a","candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0002512045,0.0001467931,0.0000937837,0.00005520759,0.0001954885,0.00005013209,0.000256602,0.00008099328,0.000003839645],"category_scores_gemma":[0.0007766036,0.0001323746,0.00005905847,0.0002549558,0.00007153287,0.000002599015,0.00005600016,0.00007877911,0.000003506646],"about_ca_system_candidate":false,"about_ca_system_consensus":false,"about_ca_system_score_codex":0.00003569759,"about_ca_system_score_gemma":0.0001219469,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_topic_score_codex":0.0002060924,"about_ca_topic_score_gemma":0.0004697139,"domain_scores_codex":[0.9988486,0.00004489137,0.0002983869,0.0003531596,0.000132494,0.0003224442],"domain_scores_gemma":[0.9991677,0.0002547114,0.00009554927,0.0003305868,0.0001240245,0.00002739806],"domain_codex":null,"domain_gemma":null,"domain_candidate":null,"domain_consensus":null,"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","study_design_scores_codex":[0.00001382365,0.000130659,0.09639013,0.00002548989,0.00001615331,0.000006895818,0.0002733682,0.04032869,0.8313344,0.00003454258,0.001356799,0.03008904],"study_design_scores_gemma":[0.002451601,0.0003629094,0.7522756,0.00005840361,0.00007095163,0.0001554299,0.0006114891,0.02988352,0.2007056,0.0009955924,0.01182621,0.0006026818],"study_design_candidate":"bench_or_experimental","study_design_consensus":null,"genre_codex":"empirical","genre_gemma":"empirical","genre_scores_codex":[0.9296453,0.001163803,0.06715498,0.0004659047,0.0001132569,0.0008094061,0.00007846191,0.00002889581,0.0005400152],"genre_scores_gemma":[0.8199071,0.000003684836,0.1788651,0.0002163355,0.0004721461,0.0002960587,0.0001428716,0.00002761012,0.00006905399],"genre_candidate":"empirical","genre_consensus":"empirical","teacher_disagreement_score":0.6558855,"threshold_uncertainty_score":0.5398079,"prediction_status":"machine_predicted_unvalidated"},"labels":[],"label_agreement":null},{"id":"W2066712955","doi":"10.1089/109065702760093852","title":"Diagnostic DNA Testing for X-Linked Ocular Albinism ( <i>OA1</i> ) with a Hierarchical Mutation Screening Protocol","year":2002,"lang":"en","type":"article","venue":"Genetic Testing","topic":"melanin and skin pigmentation","field":"Biochemistry, Genetics and Molecular Biology","cited_by":11,"is_retracted":false,"has_abstract":true,"routes":{"ca_aff":false,"ca_fund":true,"ca_venue":false,"about_ca":false},"ca_institutions":"","funders":"Institute of Genetics; Vision of Children Foundation","keywords":"Albinism; Genetics; Biology; Oculocutaneous albinism; Mutation; Point mutation; Population; Gene; Medicine","retraction":null,"screen_n_in":null,"score":{"opus":0.03885303596931249,"gpt":0.272916621176755,"spread":0.2340635852074425,"validation_status":"score_only:v0-immature-baseline"},"prediction":{"model_version":"codex-gemma-dda1882f352a","candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.000197072,0.0002108826,0.0001493032,0.00004602991,0.0002452118,0.00006552105,0.0001432351,0.0001117596,0.00001363041],"category_scores_gemma":[0.002279019,0.0001955567,0.000047143,0.0001874353,0.00006479769,0.000006089874,0.00005102907,0.00009871145,0.000006508955],"about_ca_system_candidate":false,"about_ca_system_consensus":false,"about_ca_system_score_codex":0.0000114455,"about_ca_system_score_gemma":0.0000381871,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_topic_score_codex":0.00001227496,"about_ca_topic_score_gemma":0.000005066813,"domain_scores_codex":[0.9985513,0.00007381433,0.0003280677,0.0004736011,0.0002014353,0.000371776],"domain_scores_gemma":[0.9988541,0.0004389149,0.0001750898,0.0002459475,0.0001749891,0.0001109794],"domain_codex":null,"domain_gemma":null,"domain_candidate":null,"domain_consensus":null,"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","study_design_scores_codex":[0.0001347634,0.0002019587,0.07171015,0.0002958939,0.0001190024,0.00008608096,0.0003464352,0.006887387,0.7395939,0.00003366709,0.000816224,0.1797745],"study_design_scores_gemma":[0.02524272,0.0166776,0.2291982,0.001745215,0.0005412186,0.002217413,0.0005250854,0.3495593,0.3535202,0.001659533,0.01528731,0.003826169],"study_design_candidate":"bench_or_experimental","study_design_consensus":"bench_or_experimental","genre_codex":"empirical","genre_gemma":"empirical","genre_scores_codex":[0.8209504,0.00009910654,0.1516317,0.0001146568,0.00006921964,0.02582059,0.00001364877,0.00009102388,0.001209594],"genre_scores_gemma":[0.6625074,8.182212e-7,0.3134381,0.0002278333,0.0004354995,0.02317291,0.00006365035,0.00005270133,0.0001010551],"genre_candidate":"empirical","genre_consensus":"empirical","teacher_disagreement_score":0.3860737,"threshold_uncertainty_score":0.7974569,"prediction_status":"machine_predicted_unvalidated"},"labels":[],"label_agreement":null},{"id":"W1970251066","doi":"10.1089/gte.2008.0004","title":"Screening for Hemochromatosis and Iron Overload: Satisfaction with Results Notification and Understanding of Mailed Results in Unaffected Participants of the HEIRS Study","year":2008,"lang":"en","type":"article","venue":"Genetic Testing","topic":"Iron Metabolism and Disorders","field":"Medicine","cited_by":11,"is_retracted":false,"has_abstract":true,"routes":{"ca_aff":true,"ca_fund":false,"ca_venue":false,"about_ca":false},"ca_institutions":"London Health Sciences Centre","funders":"National Center for Research Resources; National Heart, Lung, and Blood Institute","keywords":"Medicine; Transferrin saturation; Test (biology); Serum ferritin; Hemochromatosis; Vietnamese; Physical therapy; Ferritin; Family medicine; Psychology; Internal medicine","retraction":null,"screen_n_in":null,"score":{"opus":0.1022146683483286,"gpt":0.2882639413391075,"spread":0.1860492729907788,"validation_status":"score_only:v0-immature-baseline"},"prediction":{"model_version":"codex-gemma-dda1882f352a","candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0002932503,0.00009090965,0.0002105418,0.00007887142,0.000102545,0.000004694845,0.00002537385,0.00003434888,3.759015e-7],"category_scores_gemma":[0.0009016995,0.00006568601,0.00001288404,0.0002753437,0.0001082132,0.00003304711,0.00002099761,0.00005508462,3.036997e-8],"about_ca_system_candidate":false,"about_ca_system_consensus":false,"about_ca_system_score_codex":0.00001896724,"about_ca_system_score_gemma":0.00004007493,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_topic_score_codex":0.0007017509,"about_ca_topic_score_gemma":0.0004668042,"domain_scores_codex":[0.9990454,0.00006195518,0.0003616052,0.0002132125,0.0001649137,0.0001528764],"domain_scores_gemma":[0.9991576,0.0003469204,0.0002361674,0.0001742814,0.00004700431,0.00003803217],"domain_codex":null,"domain_gemma":null,"domain_candidate":null,"domain_consensus":null,"study_design_codex":"observational","study_design_gemma":"observational","study_design_scores_codex":[0.0009812072,0.0000746649,0.971657,0.0001591677,0.00001121535,0.000001822763,0.003564771,0.0005214141,0.01863767,0.0000066896,0.000006381646,0.004377934],"study_design_scores_gemma":[0.007175312,0.0004495377,0.9838227,0.0002420451,0.0001067413,0.00001629983,0.003921052,0.002015897,0.002162039,0.00002346954,2.875443e-7,0.00006460735],"study_design_candidate":"observational","study_design_consensus":"observational","genre_codex":"empirical","genre_gemma":"empirical","genre_scores_codex":[0.9980635,0.0001388829,0.0007439663,0.00006474444,0.00002013484,0.000886718,0.00001442992,0.00001288682,0.00005475064],"genre_scores_gemma":[0.9925485,0.00001390845,0.007382491,0.000007383962,0.00001030821,0.00001527935,0.000003727993,0.00001095265,0.000007510176],"genre_candidate":"empirical","genre_consensus":"empirical","teacher_disagreement_score":0.01647563,"threshold_uncertainty_score":0.2678598,"prediction_status":"machine_predicted_unvalidated"},"labels":[],"label_agreement":null},{"id":"W2093715522","doi":"10.1089/gte.2007.0003","title":"<i>HFE</i> C282Y Homozygotes Aged 25–29 Years at HEIRS Study Initial Screening","year":2007,"lang":"en","type":"article","venue":"Genetic Testing","topic":"Iron Metabolism and Disorders","field":"Medicine","cited_by":10,"is_retracted":false,"has_abstract":true,"routes":{"ca_aff":true,"ca_fund":true,"ca_venue":false,"about_ca":false},"ca_institutions":"London Health Sciences Centre; Western University","funders":"National Cancer Institute; National Heart, Lung, and Blood Institute; National Center for Research Resources; U.S. Public Health Service; London Health Sciences Centre","keywords":"Transferrin saturation; Hereditary hemochromatosis; Hemochromatosis; Medicine; HAMP; Genotyping; Ferritin; Compound heterozygosity; Transferrin; Internal medicine; Gastroenterology; Genotype; Serum ferritin; Genetics; Mutation; Anemia; Hepcidin; Biology","retraction":null,"screen_n_in":null,"score":{"opus":0.04349790020130714,"gpt":0.3037443469629396,"spread":0.2602464467616324,"validation_status":"score_only:v0-immature-baseline"},"prediction":{"model_version":"codex-gemma-dda1882f352a","candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0006209707,0.0002169432,0.0003165287,0.0001497632,0.0002241772,0.0000304254,0.0001354045,0.000083451,0.0001136627],"category_scores_gemma":[0.0008370296,0.000218553,0.0000734553,0.0004292837,0.00008932855,0.00004305681,0.0001518819,0.0002526089,0.00008502207],"about_ca_system_candidate":false,"about_ca_system_consensus":false,"about_ca_system_score_codex":0.00002876698,"about_ca_system_score_gemma":0.000059817,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_topic_score_codex":0.0002408618,"about_ca_topic_score_gemma":0.000125186,"domain_scores_codex":[0.9980881,0.0000612926,0.0004277954,0.0004000654,0.0004349946,0.000587788],"domain_scores_gemma":[0.9988896,0.0003187501,0.0001152661,0.0003733717,0.00007682003,0.0002261725],"domain_codex":null,"domain_gemma":null,"domain_candidate":null,"domain_consensus":null,"study_design_codex":"observational","study_design_gemma":"observational","study_design_scores_codex":[0.0001170909,0.0002737014,0.7444136,0.00005295443,0.00003037596,0.0007453995,0.002260415,0.0001046226,0.009326737,0.000004320845,0.0004878771,0.242183],"study_design_scores_gemma":[0.003048415,0.0003662457,0.9916764,0.00005603457,0.0001648543,0.0001533986,0.002401114,0.00006323696,0.0008781385,0.00002543963,0.0009204274,0.0002463119],"study_design_candidate":"observational","study_design_consensus":"observational","genre_codex":"empirical","genre_gemma":"empirical","genre_scores_codex":[0.9894078,0.001138238,0.001761856,0.00004227225,0.000245259,0.0005485109,0.000003849734,0.0001957545,0.006656498],"genre_scores_gemma":[0.9649332,0.000006445307,0.03352688,0.0005236871,0.0005429928,0.00001023813,0.00001124698,0.0000536851,0.0003916175],"genre_candidate":"empirical","genre_consensus":"empirical","teacher_disagreement_score":0.2472628,"threshold_uncertainty_score":0.8912333,"prediction_status":"machine_predicted_unvalidated"},"labels":[],"label_agreement":null},{"id":"W2172866610","doi":"10.1089/10906570050114849","title":"Pitfalls in the Genetic Diagnosis of Hereditary Hemochromatosis","year":2000,"lang":"en","type":"article","venue":"Genetic Testing","topic":"Iron Metabolism and Disorders","field":"Medicine","cited_by":9,"is_retracted":false,"has_abstract":true,"routes":{"ca_aff":true,"ca_fund":false,"ca_venue":false,"about_ca":false},"ca_institutions":"London Health Sciences Centre; Western University","funders":"","keywords":"Hemochromatosis; Hereditary hemochromatosis; Genotype; Genetics; Proband; Mutation; Serum iron; Biology; Population; Single-nucleotide polymorphism; Primer (cosmetics); Medicine; Gene; Internal medicine; Anemia; Chemistry","retraction":null,"screen_n_in":null,"score":{"opus":0.01868611879022654,"gpt":0.2452403264944852,"spread":0.2265542077042587,"validation_status":"score_only:v0-immature-baseline"},"prediction":{"model_version":"codex-gemma-dda1882f352a","candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0001525443,0.0001227429,0.0002221194,0.00006774866,0.00004302031,0.000008388716,0.0001546406,0.00005281575,0.0005026555],"category_scores_gemma":[0.0002400976,0.00009116019,0.0000548942,0.000410045,0.00007627663,0.00001948522,0.00001782344,0.0001069257,0.00004209435],"about_ca_system_candidate":false,"about_ca_system_consensus":false,"about_ca_system_score_codex":0.00000816352,"about_ca_system_score_gemma":0.00005741023,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_topic_score_codex":0.0003916629,"about_ca_topic_score_gemma":0.00001548015,"domain_scores_codex":[0.998896,0.00006817514,0.000331185,0.0001945053,0.0002540805,0.0002560409],"domain_scores_gemma":[0.9992589,0.0002702843,0.00005189194,0.0003337127,0.00003178234,0.00005346831],"domain_codex":null,"domain_gemma":null,"domain_candidate":null,"domain_consensus":null,"study_design_codex":"observational","study_design_gemma":"observational","study_design_scores_codex":[0.00001548123,0.0002079992,0.7141642,0.0001523011,0.000006788106,0.0000985365,0.000903374,0.0004436424,0.0008515795,0.000005351892,0.001217865,0.2819329],"study_design_scores_gemma":[0.0007876528,0.0001242278,0.9967477,0.0001040317,0.00008015869,0.0001471804,0.0003103164,0.0002266047,0.0005922932,0.000187285,0.0005908581,0.0001016552],"study_design_candidate":"observational","study_design_consensus":"observational","genre_codex":"empirical","genre_gemma":"empirical","genre_scores_codex":[0.9876378,0.005217121,0.00001570404,0.0003374459,0.00005449972,0.0002915456,0.000003804594,0.00002651046,0.006415576],"genre_scores_gemma":[0.9829243,0.0002385429,0.01580376,0.0007429888,0.000144481,0.00004944744,0.000003232542,0.00001801274,0.000075177],"genre_candidate":"empirical","genre_consensus":"empirical","teacher_disagreement_score":0.2825835,"threshold_uncertainty_score":0.5503724,"prediction_status":"machine_predicted_unvalidated"},"labels":[],"label_agreement":null},{"id":"W2037771253","doi":"10.1089/gte.2006.10.50","title":"Predictors of Belief That Genetic Test Information About Hemochromatosis Should Be Shared with Family Members","year":2006,"lang":"en","type":"article","venue":"Genetic Testing","topic":"Iron Metabolism and Disorders","field":"Medicine","cited_by":8,"is_retracted":false,"has_abstract":true,"routes":{"ca_aff":true,"ca_fund":false,"ca_venue":false,"about_ca":true},"ca_institutions":"London Health Sciences Centre; Western University","funders":"National Center for Research Resources; National Cancer Institute; National Heart, Lung, and Blood Institute","keywords":"Ethnic group; Genetic testing; Test (biology); Logistic regression; Hereditary hemochromatosis; Demography; Medicine; Family history; Pacific islanders; Hemochromatosis; Genetic genealogy; Psychology; Gerontology; Environmental health; Population; Biology","retraction":null,"screen_n_in":null,"score":{"opus":0.02102999831368181,"gpt":0.2295716478099552,"spread":0.2085416494962734,"validation_status":"score_only:v0-immature-baseline"},"prediction":{"model_version":"codex-gemma-dda1882f352a","candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0001049802,0.0002440227,0.0003424199,0.0001806662,0.00009944219,0.0000372232,0.0001301962,0.0001099863,0.00006405117],"category_scores_gemma":[0.0003003884,0.0002048419,0.00006071985,0.0004460879,0.0001333531,0.0001571426,0.00004579873,0.0001268988,0.00001103932],"about_ca_system_candidate":false,"about_ca_system_consensus":false,"about_ca_system_score_codex":0.00002790984,"about_ca_system_score_gemma":0.0001681357,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_topic_score_codex":0.0008664494,"about_ca_topic_score_gemma":0.00003143421,"domain_scores_codex":[0.9982955,0.00002014272,0.00050745,0.0002266955,0.0005746264,0.0003755515],"domain_scores_gemma":[0.9988886,0.0001619057,0.0002778586,0.0003598801,0.0001893408,0.0001224163],"domain_codex":null,"domain_gemma":null,"domain_candidate":null,"domain_consensus":null,"study_design_codex":"observational","study_design_gemma":"observational","study_design_scores_codex":[0.00003301853,0.0001122401,0.9766389,0.0004199566,0.00002052516,0.000009908727,0.000480221,0.002229493,0.009785669,0.000008121996,0.002079986,0.008181984],"study_design_scores_gemma":[0.001788884,0.0002960476,0.9910157,0.0001996521,0.0002656377,0.00007004799,0.000412161,0.001255683,0.003228427,0.00001836559,0.001230555,0.0002188047],"study_design_candidate":"observational","study_design_consensus":"observational","genre_codex":"empirical","genre_gemma":"empirical","genre_scores_codex":[0.9855685,0.001259439,0.0008144638,0.0001265636,0.0001061074,0.0005071723,0.0000509987,0.0001511794,0.01141558],"genre_scores_gemma":[0.9550335,0.0000309378,0.04404573,0.0005034221,0.0001232455,0.00003297842,0.0000888597,0.0000348607,0.0001065024],"genre_candidate":"empirical","genre_consensus":"empirical","teacher_disagreement_score":0.04323127,"threshold_uncertainty_score":0.8353211,"prediction_status":"machine_predicted_unvalidated"},"labels":[],"label_agreement":null},{"id":"W4246179640","doi":"10.1002/0471748897.ch11","title":"Susceptibility Testing","year":2005,"lang":"en","type":"other","venue":"Genetic Testing","topic":"BRCA gene mutations in cancer","field":"Biochemistry, Genetics and Molecular Biology","cited_by":8,"is_retracted":false,"has_abstract":true,"routes":{"ca_aff":true,"ca_fund":false,"ca_venue":false,"about_ca":false},"ca_institutions":"North York General Hospital","funders":"","keywords":"Penetrance; Harm; Genetic testing; Heritability; Test (biology); Genetic predisposition; Medicine; Psychology; Clinical psychology; Genetics; Social psychology; Biology; Internal medicine; Gene","retraction":null,"screen_n_in":null,"score":{"opus":0.02680863231052994,"gpt":0.2798203190592584,"spread":0.2530116867487284,"validation_status":"score_only:v0-immature-baseline"},"prediction":{"model_version":"codex-gemma-dda1882f352a","candidate_categories":["metaepi_narrow"],"consensus_categories":[],"category_scores_codex":[0.0001479597,0.000330596,0.0002164694,0.00008934965,0.00007672702,0.00003363256,0.0003375504,0.0003869187,0.0007065378],"category_scores_gemma":[0.00105993,0.0003673054,0.00006782487,0.0002355056,0.0001175633,7.692897e-7,0.0002077841,0.0001705311,0.0001319645],"about_ca_system_candidate":false,"about_ca_system_consensus":false,"about_ca_system_score_codex":0.0000709622,"about_ca_system_score_gemma":0.0004072407,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_topic_score_codex":0.0001634683,"about_ca_topic_score_gemma":0.0005079267,"domain_scores_codex":[0.9983162,0.00005588175,0.000295316,0.0007601051,0.0001793815,0.0003930754],"domain_scores_gemma":[0.9986823,0.00004824721,0.000253117,0.0008111305,0.000113487,0.00009167632],"domain_codex":null,"domain_gemma":null,"domain_candidate":null,"domain_consensus":null,"study_design_codex":"not_applicable","study_design_gemma":"not_applicable","study_design_scores_codex":[0.000005868358,0.00006458492,0.02829894,0.0001560483,0.0001202966,0.00001040665,0.00003142629,0.001127557,0.1066453,0.000003051642,0.4467403,0.4167962],"study_design_scores_gemma":[0.0004018976,0.0001857338,0.01327018,0.0002046881,0.00007860267,0.00008625151,0.00002638427,0.0003313698,0.004593546,0.00003641898,0.9799574,0.0008275037],"study_design_candidate":"not_applicable","study_design_consensus":"not_applicable","genre_codex":"other","genre_gemma":"other","genre_scores_codex":[0.01332148,0.009393633,0.00259505,0.00006338333,0.0007670264,0.000651987,0.0001086338,0.000352433,0.9727464],"genre_scores_gemma":[0.03383445,0.00006259944,0.476915,0.0003569796,0.007177246,0.0001066031,0.000157088,0.001087196,0.4803028],"genre_candidate":"other","genre_consensus":"other","teacher_disagreement_score":0.5332171,"threshold_uncertainty_score":0.9998779,"prediction_status":"machine_predicted_unvalidated"},"labels":[],"label_agreement":null},{"id":"W1983469171","doi":"10.1089/10906570260471868","title":"An Intronic Polymorphism of the <i>hMLH1</i> Gene Contributes Toward Incomplete Genetic Testing for HNPCC","year":2002,"lang":"en","type":"article","venue":"Genetic Testing","topic":"Genetic factors in colorectal cancer","field":"Medicine","cited_by":7,"is_retracted":false,"has_abstract":true,"routes":{"ca_aff":true,"ca_fund":true,"ca_venue":false,"about_ca":false},"ca_institutions":"University of Manitoba; University of Alberta","funders":"Canadian Institutes of Health Research","keywords":"Genetics; Biology; Germline mutation; Allele; Exon; Germline; Gene; Mutation; Primer (cosmetics)","retraction":null,"screen_n_in":null,"score":{"opus":0.07104514862659055,"gpt":0.2690133196678158,"spread":0.1979681710412253,"validation_status":"score_only:v0-immature-baseline"},"prediction":{"model_version":"codex-gemma-dda1882f352a","candidate_categories":["metaepi_narrow"],"consensus_categories":[],"category_scores_codex":[0.0002914721,0.0003739929,0.000585259,0.0001013191,0.0002500171,0.00004080178,0.0005369852,0.0001697295,0.0002029517],"category_scores_gemma":[0.002386977,0.0003031591,0.000169712,0.0007509943,0.0003040887,0.00003531046,0.0001204715,0.0002848272,0.00001622186],"about_ca_system_candidate":false,"about_ca_system_consensus":false,"about_ca_system_score_codex":0.0002004733,"about_ca_system_score_gemma":0.0002185388,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_topic_score_codex":0.0001938054,"about_ca_topic_score_gemma":0.00001931517,"domain_scores_codex":[0.99729,0.0001095699,0.0007517908,0.0006235386,0.0004442609,0.0007808732],"domain_scores_gemma":[0.9970981,0.0009044479,0.0003575868,0.0009045734,0.0005329121,0.0002024025],"domain_codex":null,"domain_gemma":null,"domain_candidate":null,"domain_consensus":null,"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","study_design_scores_codex":[0.00005005999,0.0001469442,0.2590844,0.000241051,0.000100018,0.000009216577,0.0003256184,0.002603949,0.5415641,0.00001020266,0.0005235758,0.1953408],"study_design_scores_gemma":[0.003755233,0.002431604,0.8179203,0.0004772071,0.0005818997,0.000433791,0.0001015155,0.08757305,0.08421946,0.0008297314,0.001101584,0.0005746548],"study_design_candidate":"observational","study_design_consensus":null,"genre_codex":"empirical","genre_gemma":"empirical","genre_scores_codex":[0.9886021,0.005306043,0.002398696,0.0006909274,0.0004987561,0.001553165,0.00005683117,0.0001394022,0.0007540556],"genre_scores_gemma":[0.8681008,0.00001346319,0.1303377,0.0006564744,0.0004722264,0.0001487501,0.000005643411,0.00008457248,0.0001804196],"genre_candidate":"empirical","genre_consensus":"empirical","teacher_disagreement_score":0.5588359,"threshold_uncertainty_score":0.9999421,"prediction_status":"machine_predicted_unvalidated"},"labels":[],"label_agreement":null},{"id":"W1967268966","doi":"10.1089/gte.2005.9.111","title":"Specific Triplex Binding Capacity of Mixed Base Sequence Duplex Nucleic Acids Used for Single-Nucleotide Polymorphism Detection","year":2005,"lang":"en","type":"article","venue":"Genetic Testing","topic":"Advanced biosensing and bioanalysis techniques","field":"Biochemistry, Genetics and Molecular Biology","cited_by":7,"is_retracted":false,"has_abstract":true,"routes":{"ca_aff":true,"ca_fund":false,"ca_venue":false,"about_ca":false},"ca_institutions":"Canadian Council of Professional Engineers","funders":"Francis Crick Institute","keywords":"DNA; Base pair; Duplex (building); Nucleic acid; Molecular biology; Polymerase chain reaction; Nucleotide; Biology; Chemistry; Genetics; Gene","retraction":null,"screen_n_in":null,"score":{"opus":0.0553610974962715,"gpt":0.2668695498538792,"spread":0.2115084523576077,"validation_status":"score_only:v0-immature-baseline"},"prediction":{"model_version":"codex-gemma-dda1882f352a","candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0002856794,0.0002353038,0.0002534564,0.0001225867,0.0001746232,0.00002882952,0.000179208,0.0001667799,0.000002247472],"category_scores_gemma":[0.0003826279,0.0002381256,0.0001600119,0.0003009682,0.0001525461,0.000008116619,0.0000658241,0.00009230144,0.00000214577],"about_ca_system_candidate":false,"about_ca_system_consensus":false,"about_ca_system_score_codex":0.00005962488,"about_ca_system_score_gemma":0.00003427285,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_topic_score_codex":0.00001705697,"about_ca_topic_score_gemma":0.00002936269,"domain_scores_codex":[0.9984074,0.00006182413,0.0004922535,0.0005110028,0.0001592017,0.0003683254],"domain_scores_gemma":[0.9989134,0.0000704788,0.0003383136,0.0004023089,0.0001882791,0.00008722067],"domain_codex":null,"domain_gemma":null,"domain_candidate":null,"domain_consensus":null,"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","study_design_scores_codex":[0.00002819839,0.00004945256,0.0009354599,0.00001927528,0.00002336503,0.000001414931,0.00001643866,0.0001424033,0.9331647,0.000001607736,0.00002998114,0.06558777],"study_design_scores_gemma":[0.0004189925,0.0003747021,0.001088792,0.00004030623,0.00004658811,0.00004988278,0.00002845642,0.00224002,0.9937522,0.00003316616,0.001646137,0.0002807943],"study_design_candidate":"bench_or_experimental","study_design_consensus":"bench_or_experimental","genre_codex":"empirical","genre_gemma":"empirical","genre_scores_codex":[0.9736037,0.0001658219,0.02561251,0.00005661889,0.00009687342,0.0002702797,0.00005332813,0.00008952695,0.0000513187],"genre_scores_gemma":[0.8290306,0.0000179664,0.1703934,0.00004182014,0.0003913778,0.00001194318,0.00003118433,0.00003566477,0.00004598614],"genre_candidate":"empirical","genre_consensus":"empirical","teacher_disagreement_score":0.1447809,"threshold_uncertainty_score":0.9710481,"prediction_status":"machine_predicted_unvalidated"},"labels":[],"label_agreement":null},{"id":"W2007457347","doi":"10.1089/gte.2006.0518","title":"The Use of Ancestral Haplotypes in the Molecular Diagnosis of Familial Breast Cancer","year":2007,"lang":"en","type":"article","venue":"Genetic Testing","topic":"BRCA gene mutations in cancer","field":"Biochemistry, Genetics and Molecular Biology","cited_by":6,"is_retracted":false,"has_abstract":true,"routes":{"ca_aff":true,"ca_fund":false,"ca_venue":false,"about_ca":false},"ca_institutions":"University of Manitoba; Shared Health","funders":"","keywords":"Haplotype; Genetics; Biology; Linkage disequilibrium; MSH2; Breast cancer; MLH1; Genotyping; Gene; Allele; Cancer; Genotype; Colorectal cancer; DNA mismatch repair","retraction":null,"screen_n_in":null,"score":{"opus":0.04316075619140967,"gpt":0.2968924416283208,"spread":0.2537316854369112,"validation_status":"score_only:v0-immature-baseline"},"prediction":{"model_version":"codex-gemma-dda1882f352a","candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0002833305,0.00008875586,0.00008404144,0.00002564592,0.00005536379,0.00001245803,0.000249999,0.00005708041,0.000002757459],"category_scores_gemma":[0.0002779344,0.00006132486,0.0000428586,0.0002336812,0.0001771461,0.000002357334,0.00005371749,0.00006553598,2.971521e-7],"about_ca_system_candidate":false,"about_ca_system_consensus":false,"about_ca_system_score_codex":0.00001839338,"about_ca_system_score_gemma":0.0001302917,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_topic_score_codex":0.000526652,"about_ca_topic_score_gemma":0.0006799871,"domain_scores_codex":[0.9991455,0.00005593272,0.0002790982,0.000165545,0.00014953,0.0002043737],"domain_scores_gemma":[0.9992229,0.0002075589,0.0001340292,0.0002930493,0.0001232246,0.00001920002],"domain_codex":null,"domain_gemma":null,"domain_candidate":null,"domain_consensus":null,"study_design_codex":"observational","study_design_gemma":"observational","study_design_scores_codex":[0.00004366174,0.00004706529,0.585369,0.00002181989,0.00003445605,0.000005280029,0.0002096053,0.01317191,0.2881719,0.00004142832,0.0002568545,0.1126271],"study_design_scores_gemma":[0.0002139951,0.00008273024,0.8241394,0.00003816658,0.00002353209,0.00002138161,0.000164241,0.0002091662,0.1730123,0.00006542398,0.001931254,0.00009850557],"study_design_candidate":"observational","study_design_consensus":"observational","genre_codex":"empirical","genre_gemma":"empirical","genre_scores_codex":[0.9964091,0.002366314,0.000682817,0.0001714953,0.0001045191,0.0001570807,0.00003136406,0.000003225594,0.00007413553],"genre_scores_gemma":[0.9935135,0.0001897708,0.006000223,0.000121028,0.0001072204,0.00004333959,0.000003182646,0.00001265445,0.000009117168],"genre_candidate":"empirical","genre_consensus":"empirical","teacher_disagreement_score":0.2387704,"threshold_uncertainty_score":0.2500755,"prediction_status":"machine_predicted_unvalidated"},"labels":[],"label_agreement":null},{"id":"W2070111915","doi":"10.1089/10906570050501506","title":"Characterization of an Interstitial Deletion del(13)(q22q32) Using Microdissection and Sequential FISH and G-Banding","year":2000,"lang":"en","type":"review","venue":"Genetic Testing","topic":"Genomic variations and chromosomal abnormalities","field":"Biochemistry, Genetics and Molecular Biology","cited_by":4,"is_retracted":false,"has_abstract":true,"routes":{"ca_aff":true,"ca_fund":false,"ca_venue":false,"about_ca":false},"ca_institutions":"Alberta Children's Hospital; McMaster University Medical Centre","funders":"","keywords":"Karyotype; Biology; Microdissection; Fluorescence in situ hybridization; Chromosome; Chromosomal translocation; G banding; Molecular biology; Abnormality; Genetics; Pathology; Chromosome abnormality; Cytogenetics; Fish <Actinopterygii>; Anatomy; Medicine; Gene","retraction":null,"screen_n_in":null,"score":{"opus":0.03798512516074791,"gpt":0.2763013061065545,"spread":0.2383161809458065,"validation_status":"score_only:v0-immature-baseline"},"prediction":{"model_version":"codex-gemma-dda1882f352a","candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0001012594,0.0002124206,0.000339843,0.00008665724,0.0001299149,0.00005866295,0.00006998942,0.0002084245,0.00001096855],"category_scores_gemma":[0.00002989329,0.000222643,0.00004840635,0.00008326789,0.00005903313,0.00000924817,0.00007028412,0.00007814247,3.124021e-7],"about_ca_system_candidate":false,"about_ca_system_consensus":false,"about_ca_system_score_codex":0.00002165496,"about_ca_system_score_gemma":0.00009573487,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_topic_score_codex":0.00009528325,"about_ca_topic_score_gemma":0.00002594549,"domain_scores_codex":[0.9989374,0.0000990049,0.0004016712,0.0003462547,0.00005858466,0.0001570448],"domain_scores_gemma":[0.9994534,0.00001192004,0.0002861562,0.0001435758,0.00005323749,0.00005171614],"domain_codex":null,"domain_gemma":null,"domain_candidate":null,"domain_consensus":null,"study_design_codex":"design_other","study_design_gemma":"not_applicable","study_design_scores_codex":[0.00001580963,0.00002807698,0.0002631219,0.002438641,0.00007837077,0.000003522557,0.0001243558,0.00006227879,0.1956172,0.000002754189,0.000001920734,0.801364],"study_design_scores_gemma":[0.006943724,0.009519297,0.02022267,0.05421146,0.01381976,0.02600171,0.001212612,0.02059957,0.109952,0.0003000906,0.7253692,0.01184787],"study_design_candidate":"design_other","study_design_consensus":null,"genre_codex":"empirical","genre_gemma":"review","genre_scores_codex":[0.8170018,0.1812419,0.001279162,0.000001377509,0.0001135982,0.0002309762,0.00009434982,0.000009876534,0.00002693104],"genre_scores_gemma":[0.1831393,0.8094613,0.005004858,0.00002477317,0.0008663302,0.00002431656,0.001360747,0.00007052033,0.00004784684],"genre_candidate":"empirical","genre_consensus":null,"teacher_disagreement_score":0.7895161,"threshold_uncertainty_score":0.9079118,"prediction_status":"machine_predicted_unvalidated"},"labels":[],"label_agreement":null},{"id":"W1982245361","doi":"10.1089/10906570050501434","title":"Apparently Unstable Normal <i>FMR1</i> Alleles in Nine Developmentally Delayed Patients: Implications for Molecular Diagnosis of the Fragile X Syndrome","year":2000,"lang":"en","type":"article","venue":"Genetic Testing","topic":"Genetics and Neurodevelopmental Disorders","field":"Biochemistry, Genetics and Molecular Biology","cited_by":2,"is_retracted":false,"has_abstract":true,"routes":{"ca_aff":true,"ca_fund":false,"ca_venue":false,"about_ca":false},"ca_institutions":"University of Alberta; Janeway Children's Health and Rehabilitation Centre; North York General Hospital","funders":"","keywords":"Fragile X syndrome; FMR1; Locus (genetics); Chromosomal fragile site; Genetics; Southern blot; Biology; Allele; Fragile x; Trinucleotide repeat expansion; Gene; Cytogenetics; Chromosome","retraction":null,"screen_n_in":null,"score":{"opus":0.008837389635489893,"gpt":0.2102472649540991,"spread":0.2014098753186092,"validation_status":"score_only:v0-immature-baseline"},"prediction":{"model_version":"codex-gemma-dda1882f352a","candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00006919984,0.0001680566,0.0001370161,0.00003487857,0.0001120177,0.00001415125,0.000314963,0.00007062116,0.0000270627],"category_scores_gemma":[0.00009461608,0.0001563685,0.00006420766,0.000246842,0.00005716627,0.000003287382,0.0001231502,0.00005262732,0.000001918221],"about_ca_system_candidate":false,"about_ca_system_consensus":false,"about_ca_system_score_codex":0.00001635351,"about_ca_system_score_gemma":0.00008760465,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_topic_score_codex":0.00004856416,"about_ca_topic_score_gemma":0.00007941233,"domain_scores_codex":[0.9988292,0.00003169791,0.0003772315,0.0003382294,0.0001094055,0.0003142377],"domain_scores_gemma":[0.9994492,0.00003042439,0.000100993,0.0002738312,0.00009310306,0.0000524479],"domain_codex":null,"domain_gemma":null,"domain_candidate":null,"domain_consensus":null,"study_design_codex":"observational","study_design_gemma":"observational","study_design_scores_codex":[0.00003361223,0.0003148664,0.7266935,0.00004420138,0.00004982336,0.000001104879,0.00008108524,0.01365209,0.2243421,0.00000585529,0.000748309,0.03403349],"study_design_scores_gemma":[0.0008722676,0.0002292858,0.9488131,0.00003414811,0.00001816666,0.00000892713,0.00002307544,0.0001057003,0.04669115,0.00009128474,0.002877489,0.0002354082],"study_design_candidate":"observational","study_design_consensus":"observational","genre_codex":"empirical","genre_gemma":"empirical","genre_scores_codex":[0.9980021,0.0004110403,0.0002929935,0.0001509303,0.00004229126,0.0005735711,0.00008353869,0.000007843841,0.0004357634],"genre_scores_gemma":[0.9857802,0.00009442682,0.01316139,0.0004279533,0.000005204858,0.0002975438,0.0001322748,0.00003063582,0.00007040571],"genre_candidate":"empirical","genre_consensus":"empirical","teacher_disagreement_score":0.2221196,"threshold_uncertainty_score":0.6376521,"prediction_status":"machine_predicted_unvalidated"},"labels":[],"label_agreement":null},{"id":"W2058872616","doi":"10.1089/gte.2004.8.229","title":"Implications of the Age Range in a Population-based <i>BRCA1</i> Testing Program with Eligibility Based on Family History of Breast and Ovarian Cancer","year":2004,"lang":"en","type":"article","venue":"Genetic Testing","topic":"BRCA gene mutations in cancer","field":"Biochemistry, Genetics and Molecular Biology","cited_by":1,"is_retracted":false,"has_abstract":true,"routes":{"ca_aff":true,"ca_fund":true,"ca_venue":false,"about_ca":false},"ca_institutions":"British Columbia Centre of Excellence for Women's Health; University of British Columbia; BC Cancer Agency","funders":"National Cancer Institute; BC Cancer Agency; Michael Smith Health Research BC","keywords":"Family history; Proband; Ovarian cancer; Breast cancer; Medicine; Population; Genetic testing; Cancer; Demography; Gynecology; Oncology; Obstetrics; Mutation; Internal medicine; Genetics; Environmental health; Biology","retraction":null,"screen_n_in":null,"score":{"opus":0.02439114135042728,"gpt":0.2766999239864109,"spread":0.2523087826359836,"validation_status":"score_only:v0-immature-baseline"},"prediction":{"model_version":"codex-gemma-dda1882f352a","candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0001387999,0.0001180931,0.000125847,0.00004674529,0.00004500169,0.000005537946,0.000133628,0.0000631077,0.000001554053],"category_scores_gemma":[0.0002212961,0.00009793499,0.00002841416,0.000306114,0.0001439821,0.000002060169,0.00003000739,0.00007386081,6.420848e-8],"about_ca_system_candidate":false,"about_ca_system_consensus":false,"about_ca_system_score_codex":0.0002479378,"about_ca_system_score_gemma":0.0009983708,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_topic_score_codex":0.002220982,"about_ca_topic_score_gemma":0.0007722715,"domain_scores_codex":[0.9991162,0.00004693785,0.0002656858,0.0003020299,0.0001194756,0.0001497053],"domain_scores_gemma":[0.9991332,0.00007234664,0.0001950885,0.0004105624,0.000159894,0.00002889031],"domain_codex":null,"domain_gemma":null,"domain_candidate":null,"domain_consensus":null,"study_design_codex":"observational","study_design_gemma":"observational","study_design_scores_codex":[0.00002936245,0.0001121796,0.760344,0.00006427606,0.000007478016,5.340121e-7,0.00005109495,0.09250049,0.118311,0.00000439291,0.00001132624,0.0285638],"study_design_scores_gemma":[0.0009025706,0.0001469328,0.9933792,0.0001655778,0.00002308743,0.0000051727,0.00001014751,0.001704427,0.003430418,0.00007217852,0.000051493,0.0001087722],"study_design_candidate":"observational","study_design_consensus":"observational","genre_codex":"empirical","genre_gemma":"empirical","genre_scores_codex":[0.9975823,0.0004570049,0.0007119266,0.0001856953,0.00004164732,0.0005234378,0.00004288359,0.00001430479,0.0004407713],"genre_scores_gemma":[0.9532659,0.00000137572,0.04626335,0.000225987,0.00003014459,0.0001754796,0.0000137069,0.00001822939,0.000005805359],"genre_candidate":"empirical","genre_consensus":"empirical","teacher_disagreement_score":0.2330352,"threshold_uncertainty_score":0.3993673,"prediction_status":"machine_predicted_unvalidated"},"labels":[],"label_agreement":null},{"id":"W2022570307","doi":"10.1089/gte.2007.0031","title":"Predicting the Performance of a Genetic Testing Service for Cancer Susceptibility","year":2007,"lang":"en","type":"article","venue":"Genetic Testing","topic":"BRCA gene mutations in cancer","field":"Biochemistry, Genetics and Molecular Biology","cited_by":1,"is_retracted":false,"has_abstract":true,"routes":{"ca_aff":true,"ca_fund":true,"ca_venue":false,"about_ca":false},"ca_institutions":"University of British Columbia; University of Toronto; BC Cancer Agency","funders":"Michael Smith Health Research BC","keywords":"Genetic testing; Service (business); Cancer; Affect (linguistics); Agency (philosophy); Population; Genetic predisposition; Medicine; Computer science; Disease; Psychology; Environmental health; Business; Internal medicine","retraction":null,"screen_n_in":null,"score":{"opus":0.03171748076523931,"gpt":0.2929666287541003,"spread":0.261249147988861,"validation_status":"score_only:v0-immature-baseline"},"prediction":{"model_version":"codex-gemma-dda1882f352a","candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0007361426,0.0001829812,0.0001492176,0.00003697807,0.0002678443,0.00001900842,0.0003607702,0.0001082987,0.000007728294],"category_scores_gemma":[0.001096297,0.0001589997,0.00005464422,0.0004506962,0.0001119998,0.000003733835,0.0001546395,0.00010824,0.000001327407],"about_ca_system_candidate":false,"about_ca_system_consensus":false,"about_ca_system_score_codex":0.00006427659,"about_ca_system_score_gemma":0.0003808257,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_topic_score_codex":0.0003028677,"about_ca_topic_score_gemma":0.0006826341,"domain_scores_codex":[0.9983945,0.00003633116,0.0005065199,0.0004365031,0.0001827337,0.0004433498],"domain_scores_gemma":[0.9980975,0.0003506519,0.0002953139,0.000508946,0.0006851881,0.00006237596],"domain_codex":null,"domain_gemma":null,"domain_candidate":null,"domain_consensus":null,"study_design_codex":"observational","study_design_gemma":"observational","study_design_scores_codex":[0.00002482514,0.00001636768,0.5120952,0.000144947,0.00002566262,3.04639e-7,0.0001853096,0.01749513,0.4142749,6.065387e-7,0.00003765879,0.05569908],"study_design_scores_gemma":[0.0004994069,0.0003892503,0.7354316,0.0001137838,0.00008359754,0.0000394827,0.0003075544,0.04011384,0.2218623,0.00003820537,0.0008470402,0.0002739752],"study_design_candidate":"observational","study_design_consensus":"observational","genre_codex":"empirical","genre_gemma":"empirical","genre_scores_codex":[0.9919755,0.00137273,0.005428303,0.00008956082,0.0002492133,0.0005626893,0.00002865963,0.0000292527,0.0002640898],"genre_scores_gemma":[0.9024379,0.00001549479,0.09647223,0.0002349308,0.000636835,0.0001109323,0.000008473456,0.00003819142,0.0000450051],"genre_candidate":"empirical","genre_consensus":"empirical","teacher_disagreement_score":0.2233364,"threshold_uncertainty_score":0.6483819,"prediction_status":"machine_predicted_unvalidated"},"labels":[],"label_agreement":null},{"id":"W1543318016","doi":"10.1002/0471748897.ch8","title":"Prenatal and Neonatal Screening","year":2005,"lang":"en","type":"other","venue":"Genetic Testing","topic":"Ethics and Legal Issues in Pediatric Healthcare","field":"Medicine","cited_by":0,"is_retracted":false,"has_abstract":true,"routes":{"ca_aff":true,"ca_fund":false,"ca_venue":false,"about_ca":false},"ca_institutions":"Université de Montréal; Lakeridge Health; York University; University of Toronto","funders":"","keywords":"Prenatal diagnosis; Prenatal screening; Neural tube; Medicine; Obstetrics; Psychology; Fetus; Pregnancy; Biology; Genetics; Embryo","retraction":null,"screen_n_in":null,"score":{"opus":0.04255221535452677,"gpt":0.3292944720711736,"spread":0.2867422567166469,"validation_status":"score_only:v0-immature-baseline"},"prediction":{"model_version":"codex-gemma-dda1882f352a","candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0001341126,0.0001999948,0.000284403,0.000142023,0.00005344563,0.00002087722,0.00006850509,0.0003691472,0.0007363009],"category_scores_gemma":[0.000569681,0.0001894535,0.00003135178,0.0001257489,0.00006866183,0.000009354245,0.00009483948,0.0006236188,0.00003423149],"about_ca_system_candidate":false,"about_ca_system_consensus":false,"about_ca_system_score_codex":0.00001637902,"about_ca_system_score_gemma":0.0001369474,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_topic_score_codex":0.0008009563,"about_ca_topic_score_gemma":0.00006203193,"domain_scores_codex":[0.9988692,0.00002315103,0.0002124696,0.0003511762,0.0002512509,0.0002927078],"domain_scores_gemma":[0.9992156,0.0001567679,0.0001179212,0.0002496237,0.00004838595,0.0002117083],"domain_codex":null,"domain_gemma":null,"domain_candidate":null,"domain_consensus":null,"study_design_codex":"design_other","study_design_gemma":"not_applicable","study_design_scores_codex":[0.000004317888,0.000008220475,0.01385078,0.00115873,0.00003089964,0.000207013,0.0002047326,0.000002586918,0.000003005805,0.00002161463,0.01925578,0.9652523],"study_design_scores_gemma":[0.0005795269,0.0001440603,0.01085103,0.002377799,0.000135007,0.0006143855,0.00005312326,0.0006308882,0.000009850092,0.00002155141,0.9842723,0.0003105089],"study_design_candidate":"not_applicable","study_design_consensus":null,"genre_codex":"other","genre_gemma":"methods","genre_scores_codex":[0.002479564,0.118714,0.001984882,0.001075957,0.0004491808,0.0008298847,0.00007840011,0.0006530001,0.8737351],"genre_scores_gemma":[0.0102013,0.0006954732,0.4934528,0.0008616347,0.007737894,0.00001670148,0.00005470992,0.0005948463,0.4863847],"genre_candidate":"other","genre_consensus":null,"teacher_disagreement_score":0.9650165,"threshold_uncertainty_score":0.8061978,"prediction_status":"machine_predicted_unvalidated"},"labels":[],"label_agreement":null},{"id":"W1494972728","doi":"10.1002/0471748897.ch4","title":"Duty of Care","year":2005,"lang":"en","type":"other","venue":"Genetic Testing","topic":"Medical Malpractice and Liability Issues","field":"Health Professions","cited_by":0,"is_retracted":false,"has_abstract":true,"routes":{"ca_aff":true,"ca_fund":false,"ca_venue":false,"about_ca":false},"ca_institutions":"Hamilton Health Sciences; McMaster University; Hamilton Medical Research Group","funders":"","keywords":"Duty; Duty of care; Health care; Standard of care; Law; Nursing; Medicine; Psychology; Political science","retraction":null,"screen_n_in":null,"score":{"opus":0.0841104858155293,"gpt":0.443921323671482,"spread":0.3598108378559527,"validation_status":"score_only:v0-immature-baseline"},"prediction":{"model_version":"codex-gemma-dda1882f352a","candidate_categories":["insufficient_payload"],"consensus_categories":[],"category_scores_codex":[0.0002026307,0.000145912,0.0003501591,0.00007672334,0.00008019229,0.00000161226,0.0001695111,0.0003893861,0.02361696],"category_scores_gemma":[0.003869826,0.0001259872,0.00003828332,0.0001215598,0.00005997296,0.000007605131,0.0000951102,0.0005277077,0.0007268612],"about_ca_system_candidate":false,"about_ca_system_consensus":false,"about_ca_system_score_codex":0.00003306911,"about_ca_system_score_gemma":0.0003140203,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_topic_score_codex":0.001347716,"about_ca_topic_score_gemma":0.0003846713,"domain_scores_codex":[0.9985598,0.0002391162,0.0004245476,0.0002314919,0.0002335833,0.0003114754],"domain_scores_gemma":[0.997767,0.001136204,0.0004799721,0.0004069905,0.0001047864,0.0001050885],"domain_codex":null,"domain_gemma":null,"domain_candidate":null,"domain_consensus":null,"study_design_codex":"not_applicable","study_design_gemma":"not_applicable","study_design_scores_codex":[0.000007797878,0.00005337918,0.08095387,0.007870818,0.00004277851,0.00001128873,0.004916355,0.000004850046,0.00007994167,0.0001008985,0.7010099,0.2049481],"study_design_scores_gemma":[0.0001758003,0.00005160313,0.007789875,0.001907068,0.00005319639,6.747505e-7,0.001993152,0.00001030792,0.000003901657,0.00001818843,0.9878764,0.0001198024],"study_design_candidate":"not_applicable","study_design_consensus":"not_applicable","genre_codex":"other","genre_gemma":"other","genre_scores_codex":[0.001572257,0.005114922,0.0000461755,0.0003973809,0.0005310006,0.0005345423,0.00002897186,0.0001889803,0.9915858],"genre_scores_gemma":[0.01541578,0.0001436271,0.07960477,0.0006293803,0.005387485,0.00008262329,0.00002778146,0.000426618,0.8982819],"genre_candidate":"other","genre_consensus":"other","teacher_disagreement_score":0.2868665,"threshold_uncertainty_score":0.9772756,"prediction_status":"machine_predicted_unvalidated"},"labels":[],"label_agreement":null},{"id":"W4247326946","doi":"10.1002/0471748897.ch2","title":"Communication","year":2005,"lang":"en","type":"other","venue":"Genetic Testing","topic":"Empathy and Medical Education","field":"Medicine","cited_by":0,"is_retracted":false,"has_abstract":true,"routes":{"ca_aff":true,"ca_fund":false,"ca_venue":false,"about_ca":false},"ca_institutions":"SickKids Foundation; Hospital for Sick Children; University of Toronto","funders":"","keywords":"Empathy; Psychology; Computer science; Social psychology","retraction":null,"screen_n_in":null,"score":{"opus":0.03841141946924328,"gpt":0.319387271775561,"spread":0.2809758523063178,"validation_status":"score_only:v0-immature-baseline"},"prediction":{"model_version":"codex-gemma-dda1882f352a","candidate_categories":["insufficient_payload"],"consensus_categories":[],"category_scores_codex":[0.00006854248,0.00009272977,0.0001428082,0.00007350175,0.00002356983,0.000004884879,0.00006928144,0.0001529149,0.002791194],"category_scores_gemma":[0.0005702448,0.00008558657,0.00002428393,0.00009732143,0.00004105435,0.000003980405,0.00002220426,0.0001860217,0.000268271],"about_ca_system_candidate":false,"about_ca_system_consensus":false,"about_ca_system_score_codex":0.00002645603,"about_ca_system_score_gemma":0.000146056,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_topic_score_codex":0.0001335286,"about_ca_topic_score_gemma":0.00001900477,"domain_scores_codex":[0.9994769,0.0000187837,0.0001291238,0.0001299774,0.0001269036,0.0001183433],"domain_scores_gemma":[0.9993463,0.00005740063,0.00009908593,0.0003711697,0.00002794985,0.00009807847],"domain_codex":null,"domain_gemma":null,"domain_candidate":null,"domain_consensus":null,"study_design_codex":"design_other","study_design_gemma":"not_applicable","study_design_scores_codex":[0.000001642007,0.00008290544,0.0008713369,0.0001429005,0.0000193415,0.000004527323,0.0009596754,9.543925e-7,0.00006159994,0.00001003297,0.3981823,0.5996628],"study_design_scores_gemma":[0.0003427657,0.00005444911,0.01612804,0.001493307,0.0001223318,0.00008414947,0.0003428071,0.000112877,0.00002504089,0.00002945263,0.9811326,0.0001321894],"study_design_candidate":"not_applicable","study_design_consensus":null,"genre_codex":"other","genre_gemma":"other","genre_scores_codex":[0.001388357,0.007828137,0.00009244179,0.0005155731,0.0001446566,0.0002377236,0.000001987838,0.0002388633,0.9895523],"genre_scores_gemma":[0.006497708,0.0002849406,0.1356968,0.0007674487,0.001555647,0.00002624739,0.00007044873,0.0002278335,0.8548729],"genre_candidate":"other","genre_consensus":"other","teacher_disagreement_score":0.5995306,"threshold_uncertainty_score":0.9981204,"prediction_status":"machine_predicted_unvalidated"},"labels":[],"label_agreement":null},{"id":"W4255685392","doi":"10.1002/0471748897.index","title":"Index","year":2005,"lang":"en","type":"paratext","venue":"Genetic Testing","topic":"Ethics in Clinical Research","field":"Medicine","cited_by":0,"is_retracted":false,"has_abstract":true,"routes":{"ca_aff":true,"ca_fund":false,"ca_venue":false,"about_ca":false},"ca_institutions":"Hamilton Health Sciences; McMaster University; Hamilton Medical Research Group","funders":"","keywords":"Library science; Index (typography); Management; Medicine; Computer science","retraction":null,"screen_n_in":null,"score":{"opus":0.5738279371604651,"gpt":0.5813650675175306,"spread":0.007537130357065491,"validation_status":"score_only:v0-immature-baseline"},"prediction":{"model_version":"codex-gemma-dda1882f352a","candidate_categories":["metaresearch","research_integrity","insufficient_payload"],"consensus_categories":["insufficient_payload"],"category_scores_codex":[0.001170366,0.0002524961,0.0005143224,0.0001612076,0.00009352048,0.00004426729,0.0003431533,0.001227326,0.006118665],"category_scores_gemma":[0.02943159,0.0002330782,0.0001194126,0.0003438362,0.000215245,0.00001047006,0.0003211345,0.004661063,0.01970913],"about_ca_system_candidate":false,"about_ca_system_consensus":false,"about_ca_system_score_codex":0.0001400842,"about_ca_system_score_gemma":0.001927488,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_topic_score_codex":0.000129335,"about_ca_topic_score_gemma":0.00004179328,"domain_scores_codex":[0.9969471,0.0000663764,0.0006369182,0.0006235853,0.001162704,0.0005632848],"domain_scores_gemma":[0.9891109,0.008859241,0.000188509,0.0008365179,0.0006788339,0.0003259464],"domain_codex":null,"domain_gemma":null,"domain_candidate":null,"domain_consensus":null,"study_design_codex":"design_other","study_design_gemma":"not_applicable","study_design_scores_codex":[0.00007604387,0.0002753774,0.02362086,0.003499979,0.0002241099,0.0003552205,0.0001379802,0.0008482048,0.001214431,0.00007941943,0.4508728,0.5187955],"study_design_scores_gemma":[0.00278965,0.00142371,0.1090725,0.009913031,0.000323332,0.0006026446,0.00006516437,0.004331951,0.0005128437,0.005039168,0.864626,0.001299977],"study_design_candidate":"not_applicable","study_design_consensus":null,"genre_codex":"other","genre_gemma":"other","genre_scores_codex":[0.00614996,0.006181518,0.0006942847,0.00176478,0.001153434,0.0005705529,0.00002070108,0.00008646606,0.9833783],"genre_scores_gemma":[0.05420477,0.00118209,0.06317696,0.001900329,0.007374564,0.00005050746,0.00005674705,0.0001513192,0.8719027],"genre_candidate":"other","genre_consensus":"other","teacher_disagreement_score":0.5174956,"threshold_uncertainty_score":0.9976352,"prediction_status":"machine_predicted_unvalidated"},"labels":[],"label_agreement":null},{"id":"W4205908186","doi":"10.1002/0471748897.refs","title":"References","year":2005,"lang":"en","type":"other","venue":"Genetic Testing","topic":"BRCA gene mutations in cancer","field":"Biochemistry, Genetics and Molecular Biology","cited_by":0,"is_retracted":false,"has_abstract":false,"routes":{"ca_aff":true,"ca_fund":false,"ca_venue":false,"about_ca":false},"ca_institutions":"Hamilton Health Sciences; McMaster University; Hamilton Medical Research Group","funders":"","keywords":"Library science; Citation; Computer science","retraction":null,"screen_n_in":null,"score":{"opus":0.02592453505266725,"gpt":0.2796768851851659,"spread":0.2537523501324987,"validation_status":"score_only:v0-immature-baseline"},"prediction":{"model_version":"codex-gemma-dda1882f352a","candidate_categories":["insufficient_payload"],"consensus_categories":[],"category_scores_codex":[0.00004912927,0.0001961097,0.000127198,0.00006846207,0.00003683687,0.00002038943,0.000242951,0.0002679531,0.001025807],"category_scores_gemma":[0.0001374263,0.000203457,0.00003959599,0.00009769428,0.00006123164,3.158928e-7,0.0001000403,0.00008695706,0.0001414171],"about_ca_system_candidate":false,"about_ca_system_consensus":false,"about_ca_system_score_codex":0.00002241853,"about_ca_system_score_gemma":0.0002229013,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_topic_score_codex":0.00006531847,"about_ca_topic_score_gemma":0.0002076457,"domain_scores_codex":[0.9990743,0.00002583754,0.0001531239,0.0004144373,0.0001160949,0.0002161787],"domain_scores_gemma":[0.999336,0.00001048365,0.0001413917,0.0004250555,0.00003848055,0.00004858048],"domain_codex":null,"domain_gemma":null,"domain_candidate":null,"domain_consensus":null,"study_design_codex":"not_applicable","study_design_gemma":"not_applicable","study_design_scores_codex":[0.000002023766,0.00001433072,0.001173491,0.00003299562,0.00006318491,0.000002938851,0.00001428716,0.0001588911,0.01172472,0.000005680013,0.7586398,0.2281677],"study_design_scores_gemma":[0.0001198803,0.00005661475,0.001118353,0.00006547054,0.0000245956,0.00002177438,0.00001146649,0.00002556638,0.001834882,0.00001650963,0.9964357,0.0002692105],"study_design_candidate":"not_applicable","study_design_consensus":"not_applicable","genre_codex":"other","genre_gemma":"other","genre_scores_codex":[0.001641607,0.01241089,0.0009279836,0.00005299362,0.0004396758,0.0001948319,0.00004433738,0.00010621,0.9841815],"genre_scores_gemma":[0.00822753,0.0002877291,0.1412706,0.0002452819,0.004116803,0.00006193673,0.0001098225,0.0004824782,0.8451979],"genre_candidate":"other","genre_consensus":"other","teacher_disagreement_score":0.2377959,"threshold_uncertainty_score":0.9998874,"prediction_status":"machine_predicted_unvalidated"},"labels":[],"label_agreement":null}]}