{"meta":{"page":1,"per_page":50,"max_per_page":100,"total":449,"total_is_capped":false,"direct_labels_cover":0,"predictions_cover":449,"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":"321fbdd93ed6","filters":{"venue":"Journal of Medical Genetics"}},"results":[{"id":"W2150580148","doi":"10.1136/jmg.2009.069013","title":"International guidelines for the diagnosis and management of hereditary haemorrhagic telangiectasia","year":2009,"lang":"en","type":"article","venue":"Journal of Medical Genetics","topic":"Vascular Anomalies and Treatments","field":"Medicine","cited_by":1075,"is_retracted":false,"has_abstract":true,"routes":{"ca_aff":true,"ca_fund":true,"ca_venue":false,"about_ca":false},"ca_institutions":"University Health Network; Children's Hospital of Eastern Ontario; University of Toronto; St. Michael's Hospital","funders":"Canadian Institutes of Health Research","keywords":"Medicine; Telangiectasia; MEDLINE; Family medicine; Health care; Disease; Pediatrics; ACVRL1; Intensive care medicine; Pathology","retraction":null,"screen_n_in":null,"score":{"opus":0.07148087992264893,"gpt":0.3812383897418931,"spread":0.3097575098192441,"validation_status":"score_only:v0-immature-baseline"},"prediction":{"model_version":"codex-gemma-dda1882f352a","candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0003169224,0.00005816298,0.0001585042,0.00003585269,0.00002026578,0.000005916911,0.000127489,0.00004549734,0.0000699403],"category_scores_gemma":[0.0001270502,0.00003130589,0.0001256077,0.00003621706,0.00003627754,0.00001225695,0.00002588343,0.00006792785,4.275462e-7],"about_ca_system_candidate":false,"about_ca_system_consensus":false,"about_ca_system_score_codex":0.00001229463,"about_ca_system_score_gemma":0.00002882007,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_topic_score_codex":0.000001975638,"about_ca_topic_score_gemma":6.140044e-7,"domain_scores_codex":[0.9989242,0.000008253644,0.0003365158,0.00005225502,0.0006066074,0.00007215644],"domain_scores_gemma":[0.9994258,0.00006093327,0.0001131858,0.00008238501,0.0002180438,0.00009959852],"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":[0.00014719,0.0003655043,0.01305551,0.00009734873,0.0013723,0.0005658191,0.00008801209,0.00003454329,0.00001444732,0.0001890511,0.04103456,0.9430357],"study_design_scores_gemma":[0.01784243,0.004985457,0.5084984,0.002045579,0.004328901,0.006200253,0.001282771,0.009964065,0.001522603,0.002055584,0.4410311,0.0002428962],"study_design_candidate":"design_other","study_design_consensus":null,"genre_codex":"empirical","genre_gemma":"empirical","genre_scores_codex":[0.716754,0.0680925,0.009028988,0.2031695,0.001432343,0.000627274,0.00001740201,0.000007907804,0.0008701212],"genre_scores_gemma":[0.8642641,0.09443785,0.03717585,0.002612006,0.001314178,0.000007373879,0.000006506576,0.0000112087,0.0001709278],"genre_candidate":"empirical","genre_consensus":"empirical","teacher_disagreement_score":0.9427928,"threshold_uncertainty_score":0.1276617,"prediction_status":"machine_predicted_unvalidated"},"labels":[],"label_agreement":null},{"id":"W2012141576","doi":"10.1136/jmg.2009.066944","title":"Apoptosis and cancer: mutations within caspase genes","year":2009,"lang":"en","type":"review","venue":"Journal of Medical Genetics","topic":"Cell death mechanisms and regulation","field":"Biochemistry, Genetics and Molecular Biology","cited_by":708,"is_retracted":false,"has_abstract":true,"routes":{"ca_aff":true,"ca_fund":true,"ca_venue":false,"about_ca":false},"ca_institutions":"St. Boniface Hospital; University of Manitoba; Children's Hospital Research Institute of Manitoba; CancerCare Manitoba; Shared Health; Research Manitoba","funders":"Canadian Institutes of Health Research; Deutsche Krebshilfe; Deutsche Forschungsgemeinschaft; Canadian Lung Association; Manitoba Health Research Council","keywords":"XIAP; Caspase; Programmed cell death; Inhibitor of apoptosis; Pyroptosis; Apoptosis; Biology; Proteases; Carcinogenesis; Cancer research; Cancer; Cancer cell; Survivin; Intrinsic apoptosis; Cell biology; Genetics; Biochemistry; Enzyme","retraction":null,"screen_n_in":null,"score":{"opus":0.02979151527133992,"gpt":0.3492372679801889,"spread":0.319445752708849,"validation_status":"score_only:v0-immature-baseline"},"prediction":{"model_version":"codex-gemma-dda1882f352a","candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0004526505,0.0002154241,0.0006304518,0.00009730845,0.00005424565,0.00002879029,0.0002435187,0.0006145533,0.00003755093],"category_scores_gemma":[0.00009362189,0.0001531977,0.0002560397,0.0000902789,0.00007427618,0.000001707395,0.00006967111,0.0002840335,0.000001056186],"about_ca_system_candidate":false,"about_ca_system_consensus":false,"about_ca_system_score_codex":0.00001978349,"about_ca_system_score_gemma":0.0006895722,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_topic_score_codex":0.000004247347,"about_ca_topic_score_gemma":0.000007707585,"domain_scores_codex":[0.9983239,0.0001012576,0.0007139075,0.0001834691,0.0005307297,0.0001467022],"domain_scores_gemma":[0.9987714,0.00002245046,0.0006220964,0.0001582876,0.0001300675,0.0002956839],"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":[0.00000417514,0.00003246561,0.000001590732,0.0006263669,0.0001290866,0.00001564163,0.0000154791,0.00002900824,0.0003056685,0.000018173,0.0005424146,0.9982799],"study_design_scores_gemma":[0.0002776592,0.0003070469,0.000002962709,0.002015992,0.0007512593,0.000566836,0.00001556854,0.00006283764,0.0008550853,0.00006136367,0.9948925,0.0001909063],"study_design_candidate":"design_other","study_design_consensus":null,"genre_codex":"review","genre_gemma":"review","genre_scores_codex":[0.001403341,0.9967318,0.001008084,0.0001525106,0.0005415771,0.0001295942,0.0000135457,0.000002017727,0.00001752869],"genre_scores_gemma":[0.0001041833,0.9965711,0.001664909,0.00009287625,0.001320681,0.000004751124,0.00004300332,0.00002573687,0.0001728035],"genre_candidate":"review","genre_consensus":"review","teacher_disagreement_score":0.998089,"threshold_uncertainty_score":0.6247221,"prediction_status":"machine_predicted_unvalidated"},"labels":[],"label_agreement":null},{"id":"W2103172754","doi":"10.1136/jmedgenet-2015-103094","title":"Hereditary diffuse gastric cancer: updated clinical guidelines with an emphasis on germline <i>CDH1</i> mutation carriers","year":2015,"lang":"en","type":"review","venue":"Journal of Medical Genetics","topic":"Gastric Cancer Management and Outcomes","field":"Medicine","cited_by":564,"is_retracted":false,"has_abstract":true,"routes":{"ca_aff":true,"ca_fund":false,"ca_venue":false,"about_ca":false},"ca_institutions":"University of British Columbia; BC Cancer Agency","funders":"Medical Research Council; ZonMw; Radboud Universitair Medisch Centrum; National Institute for Health and Care Research; Leids Universitair Medisch Centrum; Koninklijke Nederlandse Akademie van Wetenschappen; Universiteit Leiden; Cancer Research UK","keywords":"CDH1; Medicine; Breast cancer; Germline mutation; Cancer; Genetic testing; Signet ring cell carcinoma; Gastrectomy; Prophylactic Mastectomy; Invasive lobular carcinoma; Internal medicine; Oncology; Mastectomy; General surgery; Mutation; Genetics; Adenocarcinoma; Gene; Biology","retraction":null,"screen_n_in":null,"score":{"opus":0.1485630608455765,"gpt":0.4648712580982918,"spread":0.3163081972527153,"validation_status":"score_only:v0-immature-baseline"},"prediction":{"model_version":"codex-gemma-dda1882f352a","candidate_categories":["metaepi_narrow"],"consensus_categories":[],"category_scores_codex":[0.002589211,0.0005545962,0.003041035,0.0005229188,0.00004868702,0.00004313813,0.0006443427,0.0006575335,0.0003661695],"category_scores_gemma":[0.0008275533,0.0003335057,0.0006825367,0.0007306515,0.0002058464,0.00007276007,0.00009588339,0.001577694,0.00001279535],"about_ca_system_candidate":false,"about_ca_system_consensus":false,"about_ca_system_score_codex":0.0003453748,"about_ca_system_score_gemma":0.004216233,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_topic_score_codex":0.00003275408,"about_ca_topic_score_gemma":0.00004243898,"domain_scores_codex":[0.9923195,0.0003495056,0.002967258,0.0004163251,0.0035311,0.0004162895],"domain_scores_gemma":[0.9946474,0.0001990357,0.00187125,0.0005106113,0.001141925,0.001629731],"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":[0.0003088162,0.000356848,0.0004630181,0.001353348,0.0009526749,0.002522917,0.00002148366,0.00002304181,1.468627e-8,0.000001172479,0.1133056,0.8806911],"study_design_scores_gemma":[0.005718979,0.004326684,0.0001579778,0.008999721,0.007123339,0.002221852,0.00009853793,0.0001843449,1.928354e-7,0.000006256444,0.9708795,0.0002825964],"study_design_candidate":"not_applicable","study_design_consensus":null,"genre_codex":"review","genre_gemma":"review","genre_scores_codex":[0.002150332,0.9914965,0.0003578631,0.002851022,0.00238212,0.0005899357,0.00005914692,0.00003144936,0.00008163792],"genre_scores_gemma":[0.00003476019,0.9865335,0.003104011,0.001962753,0.007737476,0.00001279033,0.000205099,0.00009833254,0.0003113191],"genre_candidate":"review","genre_consensus":"review","teacher_disagreement_score":0.8804085,"threshold_uncertainty_score":0.9999117,"prediction_status":"machine_predicted_unvalidated"},"labels":[],"label_agreement":null},{"id":"W2170332740","doi":"10.1136/jmg.2009.074237","title":"Hereditary diffuse gastric cancer: updated consensus guidelines for clinical management and directions for future research","year":2010,"lang":"en","type":"article","venue":"Journal of Medical Genetics","topic":"Cancer-related gene regulation","field":"Biochemistry, Genetics and Molecular Biology","cited_by":542,"is_retracted":false,"has_abstract":true,"routes":{"ca_aff":true,"ca_fund":true,"ca_venue":false,"about_ca":false},"ca_institutions":"BC Cancer Agency","funders":"BC Cancer Agency; University College London Hospitals NHS Foundation Trust; Radboud Universiteit; Memorial Sloan-Kettering Cancer Center; Institut National de la Santé et de la Recherche Médicale; Massachusetts General Hospital; University of Leeds; Cancer Research UK; University of Nottingham; Università degli Studi di Siena; Nottingham University Hospitals NHS Trust; University of Otago","keywords":"Medicine; Breast cancer; Cancer; Invasive lobular carcinoma; Genetic testing; Germline mutation; Family history; Mammography; General surgery; Internal medicine; Oncology; Pathology; Mutation; Genetics","retraction":null,"screen_n_in":null,"score":{"opus":0.0898694985927116,"gpt":0.4592207861941303,"spread":0.3693512876014187,"validation_status":"score_only:v0-immature-baseline"},"prediction":{"model_version":"codex-gemma-dda1882f352a","candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.001993034,0.0001047533,0.0001946973,0.0001004797,0.0001131223,0.00002010844,0.0002168852,0.0004139507,0.00002173489],"category_scores_gemma":[0.0008057188,0.00008665959,0.0001349042,0.0001242333,0.0001958477,0.000001791267,0.00008838296,0.0003927497,3.07897e-7],"about_ca_system_candidate":false,"about_ca_system_consensus":false,"about_ca_system_score_codex":0.00001612333,"about_ca_system_score_gemma":0.0003203345,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_topic_score_codex":0.000004795474,"about_ca_topic_score_gemma":0.0001348929,"domain_scores_codex":[0.9982882,0.00008083445,0.0006701347,0.0002123168,0.0005168961,0.0002316462],"domain_scores_gemma":[0.9979594,0.0001122996,0.0002033219,0.0001881897,0.001245918,0.0002908684],"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":[0.0006093436,0.0002110861,0.002163441,0.00006864638,0.0004128416,0.00001103397,0.00001672193,0.00008664896,0.0123139,0.00005051929,0.6424989,0.341557],"study_design_scores_gemma":[0.003553876,0.0007917318,0.006376577,0.00004589938,0.0001452504,0.0002329615,0.0001476161,0.002098804,0.002718339,0.0002337308,0.9835321,0.0001230898],"study_design_candidate":"not_applicable","study_design_consensus":"not_applicable","genre_codex":"empirical","genre_gemma":"empirical","genre_scores_codex":[0.9533576,0.01865873,0.00338927,0.01961647,0.004392972,0.0004942463,0.00006125503,0.000005468158,0.00002403203],"genre_scores_gemma":[0.4055123,0.3341166,0.1697545,0.002256516,0.08476405,0.0002316909,0.0003062427,0.0001996962,0.002858343],"genre_candidate":"empirical","genre_consensus":"empirical","teacher_disagreement_score":0.5478452,"threshold_uncertainty_score":0.3533876,"prediction_status":"machine_predicted_unvalidated"},"labels":[],"label_agreement":null},{"id":"W2131906164","doi":"10.1136/jmg.2006.043802","title":"Features associated with germline CDKN2A mutations: a GenoMEL study of melanoma-prone families from three continents","year":2006,"lang":"en","type":"article","venue":"Journal of Medical Genetics","topic":"Cutaneous Melanoma Detection and Management","field":"Medicine","cited_by":475,"is_retracted":false,"has_abstract":true,"routes":{"ca_aff":true,"ca_fund":false,"ca_venue":false,"about_ca":false},"ca_institutions":"University of Toronto","funders":"National Cancer Institute; National Institutes of Health; Cancer Australia","keywords":"CDKN2A; Pancreatic cancer; Germline mutation; Melanoma; Incidence (geometry); Medicine; Cancer; Demography; Oncology; Internal medicine; Mutation; Genetics; Biology; Cancer research; Gene","retraction":null,"screen_n_in":null,"score":{"opus":0.01329044402511723,"gpt":0.2607995525508487,"spread":0.2475091085257315,"validation_status":"score_only:v0-immature-baseline"},"prediction":{"model_version":"codex-gemma-dda1882f352a","candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0004049112,0.0001526829,0.0005272848,0.0002060651,0.00004557515,0.00001765473,0.0001734779,0.0001278874,0.0001998092],"category_scores_gemma":[0.0002819913,0.0001058162,0.00009242543,0.0002244635,0.00009836259,0.00002146498,0.00004935067,0.0003533825,0.000002705602],"about_ca_system_candidate":false,"about_ca_system_consensus":false,"about_ca_system_score_codex":0.00006436706,"about_ca_system_score_gemma":0.0001444022,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_topic_score_codex":0.0002489178,"about_ca_topic_score_gemma":0.002087371,"domain_scores_codex":[0.9971459,0.00007194845,0.0007720541,0.0001424178,0.001696582,0.0001710818],"domain_scores_gemma":[0.998545,0.0001426808,0.0005748901,0.0001830407,0.0003688764,0.000185534],"domain_codex":null,"domain_gemma":null,"domain_candidate":null,"domain_consensus":null,"study_design_codex":"observational","study_design_gemma":"observational","study_design_scores_codex":[0.005131201,0.02437154,0.7539351,0.0002586403,0.008304179,0.01199807,0.004424326,0.002183329,0.0128864,0.00008113862,0.01454597,0.1618801],"study_design_scores_gemma":[0.01147868,0.004805298,0.9763469,0.0003067981,0.001064175,0.0004503672,0.001920026,0.000411349,0.0005951176,0.0002145401,0.002252237,0.0001545478],"study_design_candidate":"observational","study_design_consensus":"observational","genre_codex":"empirical","genre_gemma":"empirical","genre_scores_codex":[0.9950804,0.001407115,0.00148719,0.0009136954,0.0002462478,0.0003783838,0.00001084476,0.00001612987,0.0004600508],"genre_scores_gemma":[0.997991,0.0002142687,0.0007638197,0.0001561626,0.0004216842,0.000004448252,0.00002032049,0.00002118596,0.0004071367],"genre_candidate":"empirical","genre_consensus":"empirical","teacher_disagreement_score":0.2224118,"threshold_uncertainty_score":0.4315058,"prediction_status":"machine_predicted_unvalidated"},"labels":[],"label_agreement":null},{"id":"W2172085460","doi":"10.1136/jmg.2005.039669","title":"The molecular genetics of Marfan syndrome and related disorders","year":2006,"lang":"en","type":"review","venue":"Journal of Medical Genetics","topic":"Connective tissue disorders research","field":"Biochemistry, Genetics and Molecular Biology","cited_by":431,"is_retracted":false,"has_abstract":true,"routes":{"ca_aff":true,"ca_fund":true,"ca_venue":false,"about_ca":false},"ca_institutions":"McGill University","funders":"National Institute of Arthritis and Musculoskeletal and Skin Diseases; Medical Research Council; Canadian Institutes of Health Research; National Institutes of Health; National Marfan Foundation; Vlaamse regering; Deutsche Forschungsgemeinschaft; Howard Hughes Medical Institute","keywords":"Fibrillin; Marfan syndrome; Connective tissue; Molecular genetics; Connective Tissue Disorder; Pathogenesis; Pathophysiology; Mutation; Medicine; Genetics; Biology; Bioinformatics; Gene; Pathology; Internal medicine","retraction":null,"screen_n_in":null,"score":{"opus":0.01546303302534949,"gpt":0.3490478223202564,"spread":0.3335847892949069,"validation_status":"score_only:v0-immature-baseline"},"prediction":{"model_version":"codex-gemma-dda1882f352a","candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.001273568,0.0003146659,0.000928886,0.0001364393,0.00007370604,0.00003254808,0.001009402,0.0007517854,0.00003107336],"category_scores_gemma":[0.0008738586,0.000213224,0.0004859429,0.000240078,0.0005888817,0.000001614382,0.000427386,0.0007431887,0.000002199785],"about_ca_system_candidate":false,"about_ca_system_consensus":false,"about_ca_system_score_codex":0.00002362585,"about_ca_system_score_gemma":0.0008059936,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_topic_score_codex":0.000007852726,"about_ca_topic_score_gemma":0.00002790429,"domain_scores_codex":[0.9964796,0.0004536689,0.001205749,0.0002721663,0.001243219,0.0003456402],"domain_scores_gemma":[0.9980292,0.0001959933,0.000793421,0.0004496819,0.0002659424,0.000265715],"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":[0.00001402601,0.00008378487,0.00005498512,0.001218516,0.0005735747,0.0001107984,0.00001033031,0.000008388423,0.00008317601,0.00005166362,0.0009453139,0.9968454],"study_design_scores_gemma":[0.0004938504,0.0007255021,0.00009395276,0.001163621,0.0003890114,0.001174046,0.00002750938,0.00002493096,0.00005628206,0.0003682589,0.9952583,0.0002247398],"study_design_candidate":"design_other","study_design_consensus":null,"genre_codex":"review","genre_gemma":"review","genre_scores_codex":[0.005141611,0.9935294,0.0002538072,0.0002634064,0.0002449415,0.0003152123,0.00001438398,0.000001798686,0.000235397],"genre_scores_gemma":[0.002388229,0.9970665,0.0001551132,0.0000140179,0.00008731838,0.000006429748,0.00002522654,0.00006293163,0.0001942134],"genre_candidate":"review","genre_consensus":"review","teacher_disagreement_score":0.9966207,"threshold_uncertainty_score":0.8695024,"prediction_status":"machine_predicted_unvalidated"},"labels":[],"label_agreement":null},{"id":"W2551668015","doi":"10.1136/jmedgenet-2016-104178","title":"Oral pharmacological chaperone migalastat compared with enzyme replacement therapy in Fabry disease: 18-month results from the randomised phase III ATTRACT study","year":2016,"lang":"en","type":"article","venue":"Journal of Medical Genetics","topic":"Lysosomal Storage Disorders Research","field":"Medicine","cited_by":386,"is_retracted":false,"has_abstract":true,"routes":{"ca_aff":true,"ca_fund":false,"ca_venue":false,"about_ca":false},"ca_institutions":"Université de Montréal; Hôpital du Sacré-Cœur de Montréal","funders":"Novo Nordisk Fonden; Amicus Therapeutics","keywords":"Fabry disease; Enzyme replacement therapy; Medicine; Internal medicine; Bioinformatics; Pharmacology; Disease; Biology","retraction":null,"screen_n_in":null,"score":{"opus":0.0771082173706138,"gpt":0.3890547468100108,"spread":0.311946529439397,"validation_status":"score_only:v0-immature-baseline"},"prediction":{"model_version":"codex-gemma-dda1882f352a","candidate_categories":["insufficient_payload"],"consensus_categories":[],"category_scores_codex":[0.00290153,0.0002522368,0.0007520121,0.0001013985,0.00008356609,0.00003322748,0.0005791303,0.000112253,0.001874861],"category_scores_gemma":[0.001357972,0.0001035246,0.0001495448,0.0002472434,0.0003592561,0.00006214149,0.0001056453,0.0007626834,0.000008508808],"about_ca_system_candidate":false,"about_ca_system_consensus":false,"about_ca_system_score_codex":0.0001757733,"about_ca_system_score_gemma":0.000757197,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_topic_score_codex":0.00006021829,"about_ca_topic_score_gemma":0.0000702266,"domain_scores_codex":[0.9938569,0.0007436105,0.001170009,0.0003373167,0.003435261,0.0004569002],"domain_scores_gemma":[0.9966537,0.001316233,0.0004116388,0.0003618497,0.0002812762,0.0009753319],"domain_codex":null,"domain_gemma":null,"domain_candidate":null,"domain_consensus":null,"study_design_codex":"randomized_trial","study_design_gemma":"randomized_trial","study_design_scores_codex":[0.7880229,0.01885327,0.060974,0.00001738664,0.001419666,0.007734738,0.00306131,0.00005792003,0.007410342,0.000001035333,0.01827095,0.0941765],"study_design_scores_gemma":[0.848121,0.0140687,0.1240516,0.0006174115,0.0003906019,0.0001069918,0.002047012,0.001846228,0.00108441,0.00002066991,0.007374652,0.0002707351],"study_design_candidate":"randomized_trial","study_design_consensus":"randomized_trial","genre_codex":"empirical","genre_gemma":"empirical","genre_scores_codex":[0.9769949,0.003369908,0.0007874217,0.01706815,0.0001759086,0.001508976,0.0000339634,0.00001214162,0.00004862057],"genre_scores_gemma":[0.9947729,0.003524859,0.0001476826,0.0008717899,0.0004839004,0.00003259171,0.00001050036,0.00002637392,0.0001294538],"genre_candidate":"empirical","genre_consensus":"empirical","teacher_disagreement_score":0.09390577,"threshold_uncertainty_score":0.9990376,"prediction_status":"machine_predicted_unvalidated"},"labels":[],"label_agreement":null},{"id":"W2138170649","doi":"10.1136/jmedgenet-2011-100223","title":"What can exome sequencing do for you?","year":2011,"lang":"en","type":"review","venue":"Journal of Medical Genetics","topic":"Genomics and Rare Diseases","field":"Biochemistry, Genetics and Molecular Biology","cited_by":382,"is_retracted":false,"has_abstract":true,"routes":{"ca_aff":true,"ca_fund":true,"ca_venue":false,"about_ca":false},"ca_institutions":"McGill University; Montreal Children's Hospital; McGill University and Génome Québec Innovation Centre","funders":"Canadian Institutes of Health Research","keywords":"Exome sequencing; Exome; Human genome; Personal genomics; DNA sequencing; Genome; Human genetics; Biology; Computational biology; Personalized medicine; Mendelian inheritance; Genetics; Data science; Computer science; Gene; Mutation","retraction":null,"screen_n_in":null,"score":{"opus":0.06384831906300094,"gpt":0.3476388436216152,"spread":0.2837905245586143,"validation_status":"score_only:v0-immature-baseline"},"prediction":{"model_version":"codex-gemma-dda1882f352a","candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0006864348,0.0002994198,0.0008995218,0.0001016116,0.00004864206,0.00007872899,0.0008281898,0.0007131119,0.00006316887],"category_scores_gemma":[0.0003249289,0.0002159637,0.0008773243,0.00006270428,0.00009238618,0.000002702357,0.0001698849,0.0003204917,0.000003148224],"about_ca_system_candidate":false,"about_ca_system_consensus":false,"about_ca_system_score_codex":0.00005053495,"about_ca_system_score_gemma":0.002367205,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_topic_score_codex":0.000001699304,"about_ca_topic_score_gemma":0.000004428241,"domain_scores_codex":[0.9980249,0.00008546638,0.0008977752,0.0002547023,0.0004388319,0.0002982799],"domain_scores_gemma":[0.9981246,0.00003771476,0.0007380823,0.0003254693,0.0002474769,0.0005266304],"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":[0.00001895462,0.00006180692,0.000002534156,0.00284805,0.0004424771,0.0001025069,0.00005322708,0.000002442383,0.00002868122,0.00003889613,0.004586312,0.9918141],"study_design_scores_gemma":[0.0003134622,0.0004031048,8.733564e-7,0.003712045,0.0006651393,0.000908821,0.00008664811,0.000003008481,0.0000432958,0.00009215694,0.9935259,0.0002455752],"study_design_candidate":"not_applicable","study_design_consensus":null,"genre_codex":"review","genre_gemma":"review","genre_scores_codex":[0.0006097044,0.9967031,0.0003727194,0.00006145349,0.001921519,0.0002395266,0.00005715909,0.000001808294,0.00003304827],"genre_scores_gemma":[0.00006807132,0.996294,0.001054234,0.0002124944,0.002013617,0.00001175313,0.00008254608,0.00006263172,0.000200607],"genre_candidate":"review","genre_consensus":"review","teacher_disagreement_score":0.9915686,"threshold_uncertainty_score":0.8806743,"prediction_status":"machine_predicted_unvalidated"},"labels":[],"label_agreement":null},{"id":"W2143723459","doi":"10.1136/jmg.2005.030833","title":"Hereditary haemorrhagic telangiectasia: current views on genetics and mechanisms of disease","year":2005,"lang":"en","type":"review","venue":"Journal of Medical Genetics","topic":"Vascular Anomalies and Treatments","field":"Medicine","cited_by":377,"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; SickKids Foundation; St. Michael's Hospital","funders":"","keywords":"Genetics; Current (fluid); Telangiectasia; Disease; Inherited disease; Medical genetics; Biology; Medicine; Dermatology; Pathology; Gene","retraction":null,"screen_n_in":null,"score":{"opus":0.07792309639574142,"gpt":0.3896614904444329,"spread":0.3117383940486915,"validation_status":"score_only:v0-immature-baseline"},"prediction":{"model_version":"codex-gemma-dda1882f352a","candidate_categories":["metaepi_narrow"],"consensus_categories":[],"category_scores_codex":[0.0005139742,0.0004185289,0.002137848,0.0002458535,0.0000325781,0.00001238622,0.0002982233,0.0003642706,0.0002257763],"category_scores_gemma":[0.0001991592,0.0002613226,0.001003324,0.0001477022,0.0001157646,0.00001452171,0.0001220828,0.0008351454,0.00001625481],"about_ca_system_candidate":false,"about_ca_system_consensus":false,"about_ca_system_score_codex":0.00009612124,"about_ca_system_score_gemma":0.000949911,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_topic_score_codex":6.99337e-7,"about_ca_topic_score_gemma":0.000001035392,"domain_scores_codex":[0.9961112,0.0001623659,0.001350982,0.0002484018,0.001859611,0.0002674367],"domain_scores_gemma":[0.9974256,0.0001141367,0.0008083824,0.000391954,0.0001515742,0.00110836],"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":[0.00003325677,0.0006111037,0.00002950807,0.00691313,0.0006526225,0.001234973,0.00001845848,0.000001636633,1.046563e-7,0.00005222042,0.001238505,0.9892145],"study_design_scores_gemma":[0.001690235,0.001325065,0.0001331637,0.02301082,0.008218178,0.002514643,0.00001311341,0.00005898911,0.000003443208,0.0002266643,0.9625931,0.0002125188],"study_design_candidate":"design_other","study_design_consensus":null,"genre_codex":"review","genre_gemma":"review","genre_scores_codex":[0.0003310727,0.9973944,0.0005237451,0.0003546239,0.0008247329,0.0004552392,0.00005148529,0.000005307291,0.00005937367],"genre_scores_gemma":[0.0002285504,0.9964001,0.001669351,0.0001310066,0.0014161,0.000006031451,0.00004203825,0.00005909658,0.00004770809],"genre_candidate":"review","genre_consensus":"review","teacher_disagreement_score":0.989002,"threshold_uncertainty_score":0.9999839,"prediction_status":"machine_predicted_unvalidated"},"labels":[],"label_agreement":null},{"id":"W2172267891","doi":"10.1136/jmg.40.8.575","title":"Molecular characterisation of the 22q13 deletion syndrome supports the role of haploinsufficiency of <i>SHANK3/PROSAP2</i> in the major neurological symptoms","year":2003,"lang":"en","type":"article","venue":"Journal of Medical Genetics","topic":"Congenital heart defects research","field":"Biochemistry, Genetics and Molecular Biology","cited_by":376,"is_retracted":false,"has_abstract":true,"routes":{"ca_aff":true,"ca_fund":true,"ca_venue":false,"about_ca":false},"ca_institutions":"University of Alberta","funders":"Medical Research Council; Canadian Institutes of Health Research; Medical Research Council Canada","keywords":"Haploinsufficiency; Hypotonia; Breakpoint; Genetics; Biology; Gene; Medicine; Phenotype; Chromosome","retraction":null,"screen_n_in":null,"score":{"opus":0.006296182625673834,"gpt":0.2548098591358677,"spread":0.2485136765101938,"validation_status":"score_only:v0-immature-baseline"},"prediction":{"model_version":"codex-gemma-dda1882f352a","candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.001754004,0.0001008898,0.0002138165,0.00005102788,0.00004347597,0.000007093997,0.0006441927,0.0001884022,0.00004089419],"category_scores_gemma":[0.0008302301,0.00005098574,0.0001833883,0.0002446324,0.0003280166,0.000003567761,0.0001490945,0.0003525857,3.851529e-7],"about_ca_system_candidate":false,"about_ca_system_consensus":false,"about_ca_system_score_codex":0.000006548549,"about_ca_system_score_gemma":0.0002704191,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_topic_score_codex":0.000005534289,"about_ca_topic_score_gemma":0.000007403519,"domain_scores_codex":[0.9973454,0.000519963,0.0006400435,0.0001225942,0.001178593,0.0001934065],"domain_scores_gemma":[0.9989362,0.00008077783,0.0003630052,0.0003397788,0.0002101401,0.00007005322],"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":[0.0001196256,0.0007464411,0.03282454,0.00006540718,0.0000688064,0.00005619977,0.0003512434,0.0001438594,0.9568506,0.0002729831,0.0000601787,0.008440132],"study_design_scores_gemma":[0.001634112,0.00641219,0.2492346,0.0001406681,0.0001411674,0.002653969,0.0004369271,0.001092738,0.7291452,0.0008353326,0.008064984,0.00020804],"study_design_candidate":"bench_or_experimental","study_design_consensus":"bench_or_experimental","genre_codex":"empirical","genre_gemma":"empirical","genre_scores_codex":[0.9968066,0.00192562,0.0001277678,0.0006915022,0.00009795698,0.0002250862,0.000005624079,6.470009e-7,0.0001192523],"genre_scores_gemma":[0.99934,0.0003447131,0.00004564284,0.000208931,0.00003709821,0.000003913091,0.000002426164,0.000008798291,0.000008505956],"genre_candidate":"empirical","genre_consensus":"empirical","teacher_disagreement_score":0.2277054,"threshold_uncertainty_score":0.2079138,"prediction_status":"machine_predicted_unvalidated"},"labels":[],"label_agreement":null},{"id":"W2093392185","doi":"10.1136/jmedgenet-2012-101339","title":"High cumulative risks of cancer in patients with <i>PTEN</i> hamartoma tumour syndrome","year":2013,"lang":"en","type":"article","venue":"Journal of Medical Genetics","topic":"PI3K/AKT/mTOR signaling in cancer","field":"Biochemistry, Genetics and Molecular Biology","cited_by":369,"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; Institut Bergonié; Institut National Du Cancer","keywords":"PTEN; Cowden syndrome; Thyroid cancer; Breast cancer; Medicine; Cancer; Oncology; Internal medicine; Endometrial cancer; Cumulative incidence; Germline mutation; Cancer syndrome; Biology; Genetics; Cohort; Mutation; PI3K/AKT/mTOR pathway; Gene","retraction":null,"screen_n_in":null,"score":{"opus":0.01406470137501465,"gpt":0.2973051191653137,"spread":0.283240417790299,"validation_status":"score_only:v0-immature-baseline"},"prediction":{"model_version":"codex-gemma-dda1882f352a","candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0003196823,0.0001534602,0.0003308025,0.00007569829,0.00001790046,0.00001148037,0.0003824587,0.0001956474,0.0003133293],"category_scores_gemma":[0.0001491819,0.0001125545,0.00007824608,0.0001296238,0.0001593185,0.00000636299,0.00008777621,0.0002997218,0.000003172303],"about_ca_system_candidate":false,"about_ca_system_consensus":false,"about_ca_system_score_codex":0.00004010168,"about_ca_system_score_gemma":0.0003548352,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_topic_score_codex":0.0001573002,"about_ca_topic_score_gemma":0.00005949392,"domain_scores_codex":[0.9979297,0.00008366822,0.0005993062,0.0001639602,0.000987463,0.0002359081],"domain_scores_gemma":[0.9986233,0.00003304147,0.0004774845,0.0001767645,0.0004610311,0.0002283827],"domain_codex":null,"domain_gemma":null,"domain_candidate":null,"domain_consensus":null,"study_design_codex":"observational","study_design_gemma":"observational","study_design_scores_codex":[0.0005876032,0.0007519452,0.9246389,0.0001057597,0.0005643052,0.0001187563,0.000157833,0.007128126,0.03688822,0.00001305142,0.005530116,0.02351535],"study_design_scores_gemma":[0.005640221,0.002998615,0.9249295,0.0005174462,0.00009281789,0.00006806663,0.00005060186,0.0004073744,0.06314246,0.0001396379,0.001697113,0.0003161479],"study_design_candidate":"observational","study_design_consensus":"observational","genre_codex":"empirical","genre_gemma":"empirical","genre_scores_codex":[0.9970185,0.001697327,0.0003491153,0.000402523,0.0003368433,0.0001445839,0.00001867967,0.000001708942,0.00003078731],"genre_scores_gemma":[0.997959,0.0004819232,0.001005413,0.0002645961,0.0002180824,0.000007408384,0.000005703472,0.00002382628,0.00003411595],"genre_candidate":"empirical","genre_consensus":"empirical","teacher_disagreement_score":0.02625424,"threshold_uncertainty_score":0.4589841,"prediction_status":"machine_predicted_unvalidated"},"labels":[],"label_agreement":null},{"id":"W2123354624","doi":"10.1136/jmg.2004.018275","title":"Germline E-cadherin mutations in hereditary diffuse gastric cancer: assessment of 42 new families and review of genetic screening criteria","year":2004,"lang":"en","type":"article","venue":"Journal of Medical Genetics","topic":"Wnt/β-catenin signaling in development and cancer","field":"Biochemistry, Genetics and Molecular Biology","cited_by":363,"is_retracted":false,"has_abstract":true,"routes":{"ca_aff":true,"ca_fund":true,"ca_venue":false,"about_ca":false},"ca_institutions":"University of Alberta; Mount Sinai Hospital; Vancouver General Hospital; Lunenfeld-Tanenbaum Research Institute; University of Calgary; Children's Hospital of Eastern Ontario; McGill University; Children's Hospital of Winnipeg; Victoria General Hospital; University of British Columbia; University of Toronto; BC Cancer Agency","funders":"Genome British Columbia; Michael Smith Health Research BC; Genome Canada","keywords":"CDH1; Cancer; Genetics; Germline mutation; Penetrance; Missense mutation; Breast cancer; Biology; Mutation; Genetic counseling; Exon; Phenotype; Cancer research; Gene; Cadherin","retraction":null,"screen_n_in":null,"score":{"opus":0.01983209760705076,"gpt":0.3352254763491007,"spread":0.31539337874205,"validation_status":"score_only:v0-immature-baseline"},"prediction":{"model_version":"codex-gemma-dda1882f352a","candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0004609139,0.0001217494,0.0003389493,0.00009021051,0.00001592826,0.000005522546,0.0002358567,0.0001236871,0.0001028731],"category_scores_gemma":[0.000155639,0.0001045391,0.00007976808,0.0001697996,0.0001170944,0.0000042237,0.00008747254,0.0001710386,1.032784e-7],"about_ca_system_candidate":false,"about_ca_system_consensus":false,"about_ca_system_score_codex":0.00002522382,"about_ca_system_score_gemma":0.001027864,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_topic_score_codex":0.00005148554,"about_ca_topic_score_gemma":0.00002960442,"domain_scores_codex":[0.9982628,0.0000572638,0.0008330455,0.0001298219,0.0005691849,0.0001478953],"domain_scores_gemma":[0.9991342,0.0000237371,0.0003820288,0.0001140757,0.0001770477,0.0001688747],"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":[0.0003436629,0.001234565,0.2435864,0.007545143,0.001021846,0.0003204657,0.0009188528,0.007812547,0.4055415,0.00004163642,0.01279715,0.3188362],"study_design_scores_gemma":[0.01874561,0.003667208,0.8128406,0.03489481,0.0007143292,0.001112373,0.0007377773,0.000938244,0.106056,0.0007420472,0.01846671,0.001084211],"study_design_candidate":"observational","study_design_consensus":null,"genre_codex":"empirical","genre_gemma":"empirical","genre_scores_codex":[0.8738847,0.1148789,0.009979337,0.0009299151,0.0001953198,0.00009466631,0.000009025396,0.00000126283,0.00002685407],"genre_scores_gemma":[0.6625656,0.2919714,0.04467488,0.000358651,0.0003713419,0.000004409558,0.00001258346,0.00001561093,0.00002551276],"genre_candidate":"empirical","genre_consensus":"empirical","teacher_disagreement_score":0.5692543,"threshold_uncertainty_score":0.426298,"prediction_status":"machine_predicted_unvalidated"},"labels":[],"label_agreement":null},{"id":"W2096465437","doi":"10.1136/jmg.40.12.865","title":"Molecular and functional analysis identifies ALK-1 as the predominant cause of pulmonary hypertension related to hereditary haemorrhagic telangiectasia","year":2003,"lang":"en","type":"article","venue":"Journal of Medical Genetics","topic":"Vascular Anomalies and Treatments","field":"Medicine","cited_by":358,"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":"Tekes; Academy of Finland; British Heart Foundation","keywords":"Missense mutation; Endoglin; BMPR2; Compound heterozygosity; Biology; Mutation; Cancer research; ACVRL1; Genetics; Pulmonary hypertension; Proband; Germline mutation; Pathology; Medicine; Gene; Internal medicine","retraction":null,"screen_n_in":null,"score":{"opus":0.01405887534068585,"gpt":0.2623549172237493,"spread":0.2482960418830634,"validation_status":"score_only:v0-immature-baseline"},"prediction":{"model_version":"codex-gemma-dda1882f352a","candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0005455279,0.0001155976,0.0003947714,0.0001721657,0.00005113359,0.000009570246,0.00008329166,0.0001260913,0.0002896361],"category_scores_gemma":[0.0004198476,0.00006597002,0.0002779015,0.0003587076,0.0001020878,0.00002039249,0.00004434324,0.00021697,0.000006337434],"about_ca_system_candidate":false,"about_ca_system_consensus":false,"about_ca_system_score_codex":0.00002294378,"about_ca_system_score_gemma":0.0001541855,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_topic_score_codex":0.0000203535,"about_ca_topic_score_gemma":0.000004583328,"domain_scores_codex":[0.9980279,0.000110925,0.0004874222,0.000128649,0.00110452,0.000140584],"domain_scores_gemma":[0.9990444,0.00008033746,0.0001588594,0.0002085399,0.0002092823,0.0002986405],"domain_codex":null,"domain_gemma":null,"domain_candidate":null,"domain_consensus":null,"study_design_codex":"observational","study_design_gemma":"observational","study_design_scores_codex":[0.003816294,0.008167797,0.5280415,0.0007951712,0.08619639,0.1609183,0.004506694,0.01024245,0.0628792,0.001462107,0.01642937,0.1165448],"study_design_scores_gemma":[0.009597573,0.003400989,0.7980319,0.0007800767,0.03333549,0.1039952,0.002787895,0.008569198,0.03104594,0.002076194,0.005859562,0.0005200225],"study_design_candidate":"observational","study_design_consensus":"observational","genre_codex":"empirical","genre_gemma":"empirical","genre_scores_codex":[0.9844652,0.01192321,0.0003759841,0.002639522,0.0002244583,0.000126142,0.00000255125,0.000003095734,0.000239769],"genre_scores_gemma":[0.9978472,0.001110882,0.0004277661,0.0003899219,0.00005023908,0.000001534367,0.000006400848,0.00001200324,0.0001540604],"genre_candidate":"empirical","genre_consensus":"empirical","teacher_disagreement_score":0.2699904,"threshold_uncertainty_score":0.3171312,"prediction_status":"machine_predicted_unvalidated"},"labels":[],"label_agreement":null},{"id":"W2118321207","doi":"10.1136/jmg.2009.069369","title":"Phenotypic spectrum associated with de novo and inherited deletions and duplications at 16p11.2 in individuals ascertained for diagnosis of autism spectrum disorder","year":2009,"lang":"en","type":"article","venue":"Journal of Medical Genetics","topic":"Genomic variations and chromosomal abnormalities","field":"Biochemistry, Genetics and Molecular Biology","cited_by":351,"is_retracted":false,"has_abstract":true,"routes":{"ca_aff":true,"ca_fund":true,"ca_venue":false,"about_ca":false},"ca_institutions":"Memorial University of Newfoundland; McMaster University; University of Toronto; SickKids Foundation; Hospital for Sick Children; St. John’s Health Sciences Centre","funders":"Canadian Institutes of Health Research","keywords":"Phenotype; Autism spectrum disorder; Genetics; Biology; Copy-number variation; Autism; Gene duplication; Heritability of autism; Gene; Medicine; Genome; Psychiatry","retraction":null,"screen_n_in":null,"score":{"opus":0.007442626267632695,"gpt":0.2431433710956851,"spread":0.2357007448280524,"validation_status":"score_only:v0-immature-baseline"},"prediction":{"model_version":"codex-gemma-dda1882f352a","candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0003494822,0.00009448702,0.0001888795,0.0000713192,0.00006118113,0.00001309285,0.0001148557,0.0001663862,0.00002403153],"category_scores_gemma":[0.0002199607,0.00007979345,0.00003933533,0.00009850599,0.00008725203,0.000003662021,0.00004119855,0.0001037084,8.740157e-8],"about_ca_system_candidate":false,"about_ca_system_consensus":false,"about_ca_system_score_codex":0.00002934846,"about_ca_system_score_gemma":0.0001547138,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_topic_score_codex":0.00001145972,"about_ca_topic_score_gemma":0.000312336,"domain_scores_codex":[0.9991174,0.00004934812,0.0003556302,0.0001118568,0.0001910874,0.0001746609],"domain_scores_gemma":[0.9994553,0.00006634855,0.0002103398,0.00009176871,0.0000445421,0.0001317437],"domain_codex":null,"domain_gemma":null,"domain_candidate":null,"domain_consensus":null,"study_design_codex":"observational","study_design_gemma":"observational","study_design_scores_codex":[0.0001083309,0.0006324259,0.986167,0.00003789785,0.0002543146,0.00000823738,0.0007063353,0.0005125199,0.006223013,0.001824357,0.0003684489,0.003157156],"study_design_scores_gemma":[0.002879081,0.001496187,0.9833077,0.00009595054,0.0001084076,0.0001536597,0.0001941993,0.0004027158,0.005334232,0.003090705,0.002774253,0.0001629654],"study_design_candidate":"observational","study_design_consensus":"observational","genre_codex":"empirical","genre_gemma":"empirical","genre_scores_codex":[0.9873053,0.00182807,0.002021076,0.008641165,0.00002135002,0.0001261767,0.00003868748,0.000001876778,0.00001625211],"genre_scores_gemma":[0.9959195,0.002348278,0.001373746,0.0002088629,0.00006261327,0.00000914516,0.00002373179,0.000008959196,0.00004512081],"genre_candidate":"empirical","genre_consensus":"empirical","teacher_disagreement_score":0.008614197,"threshold_uncertainty_score":0.3253882,"prediction_status":"machine_predicted_unvalidated"},"labels":[],"label_agreement":null},{"id":"W2109917395","doi":"10.1136/jmg.39.3.178","title":"Prevalence of <i>SDHB, SDHC</i>, and <i>SDHD</i> germline mutations in clinic patients with head and neck paragangliomas","year":2002,"lang":"en","type":"article","venue":"Journal of Medical Genetics","topic":"Adrenal and Paraganglionic Tumors","field":"Medicine","cited_by":341,"is_retracted":false,"has_abstract":true,"routes":{"ca_aff":true,"ca_fund":false,"ca_venue":false,"about_ca":false},"ca_institutions":"Alberta Health Services","funders":"National Institute of Dental and Craniofacial Research; University of Pittsburgh","keywords":"SDHD; SDHB; Paraganglioma; Genetics; Germline mutation; Mutation; Germline; Biology; Medicine; Gene; Pathology","retraction":null,"screen_n_in":null,"score":{"opus":0.02016764814496622,"gpt":0.2874909969308829,"spread":0.2673233487859167,"validation_status":"score_only:v0-immature-baseline"},"prediction":{"model_version":"codex-gemma-dda1882f352a","candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0003677392,0.0001217882,0.0003815185,0.0001449603,0.00002405895,0.000006234266,0.00009994035,0.0001155554,0.000286215],"category_scores_gemma":[0.0003285653,0.00008213244,0.00004602593,0.0002299373,0.000270111,0.00004633882,0.00003861608,0.0003817787,0.00000271649],"about_ca_system_candidate":false,"about_ca_system_consensus":false,"about_ca_system_score_codex":0.00001299524,"about_ca_system_score_gemma":0.00009351278,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_topic_score_codex":0.000003574443,"about_ca_topic_score_gemma":0.000007408889,"domain_scores_codex":[0.9980363,0.00005409434,0.0007241386,0.0001322533,0.0008790488,0.0001741516],"domain_scores_gemma":[0.9988006,0.0001795118,0.0003302759,0.0001141693,0.0001863927,0.0003890001],"domain_codex":null,"domain_gemma":null,"domain_candidate":null,"domain_consensus":null,"study_design_codex":"observational","study_design_gemma":"observational","study_design_scores_codex":[0.0005043499,0.0013146,0.9727488,0.0006693181,0.0000956232,0.003980896,0.001167421,0.00002944213,0.00002609264,0.00001407556,0.001040013,0.0184094],"study_design_scores_gemma":[0.009109718,0.002826807,0.9794869,0.001368304,0.000218957,0.005127279,0.00007163575,0.0008393897,0.0002324693,0.00009626342,0.0004935999,0.0001286692],"study_design_candidate":"observational","study_design_consensus":"observational","genre_codex":"empirical","genre_gemma":"empirical","genre_scores_codex":[0.9917529,0.006472467,0.00006908579,0.001348528,0.00007473522,0.0001377089,0.000007692892,0.00000347222,0.0001333905],"genre_scores_gemma":[0.9962119,0.00161264,0.00149667,0.0003729774,0.0001187453,0.000001187018,0.000001810284,0.00001235968,0.0001716796],"genre_candidate":"empirical","genre_consensus":"empirical","teacher_disagreement_score":0.01828073,"threshold_uncertainty_score":0.3349264,"prediction_status":"machine_predicted_unvalidated"},"labels":[],"label_agreement":null},{"id":"W2172066856","doi":"10.1136/jmg.39.11.796","title":"Novel <i>ATP6V1B1</i> and <i>ATP6V0A4</i> mutations in autosomal recessive distal renal tubular acidosis with new evidence for hearing loss","year":2002,"lang":"en","type":"article","venue":"Journal of Medical Genetics","topic":"Ion Transport and Channel Regulation","field":"Biochemistry, Genetics and Molecular Biology","cited_by":317,"is_retracted":false,"has_abstract":true,"routes":{"ca_aff":true,"ca_fund":false,"ca_venue":false,"about_ca":false},"ca_institutions":"Centre Hospitalier Universitaire Sainte-Justine","funders":"National Institute on Deafness and Other Communication Disorders; Wellcome Trust; National Institutes of Health; Harvard University","keywords":"Distal renal tubular acidosis; Hearing loss; Renal tubular acidosis; Medicine; Endocrinology; Mutation; Internal medicine; Genetics; Acidosis; Biology; Audiology; Gene","retraction":null,"screen_n_in":null,"score":{"opus":0.03570447356672106,"gpt":0.2852095234986803,"spread":0.2495050499319592,"validation_status":"score_only:v0-immature-baseline"},"prediction":{"model_version":"codex-gemma-dda1882f352a","candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0002705784,0.0001198372,0.0001776164,0.00005677591,0.00005076788,0.00002463825,0.0001605135,0.0001805513,0.00002388744],"category_scores_gemma":[0.0001447535,0.0000966174,0.00006331225,0.0001036096,0.0001120959,0.00001271721,0.00002541613,0.0001661882,3.450406e-7],"about_ca_system_candidate":false,"about_ca_system_consensus":false,"about_ca_system_score_codex":0.00001462052,"about_ca_system_score_gemma":0.0001462463,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_topic_score_codex":0.000007724473,"about_ca_topic_score_gemma":0.00007010986,"domain_scores_codex":[0.9987628,0.00001793943,0.0003900946,0.0001690395,0.0004720737,0.0001879792],"domain_scores_gemma":[0.999321,0.00004298568,0.0001782223,0.00009712937,0.0001237128,0.0002369788],"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":[0.001746314,0.0007332283,0.05898001,0.000291256,0.0003551488,0.0002267401,0.001794607,0.006325346,0.8549216,0.0001230909,0.003975283,0.07052732],"study_design_scores_gemma":[0.03213719,0.01042444,0.1114586,0.004489622,0.0008569277,0.00540206,0.001049473,0.02490984,0.7412326,0.0008455063,0.06519511,0.001998547],"study_design_candidate":"bench_or_experimental","study_design_consensus":"bench_or_experimental","genre_codex":"empirical","genre_gemma":"empirical","genre_scores_codex":[0.9173489,0.004926519,0.07447094,0.002983262,0.0001241059,0.0001219133,0.000007219827,0.000002837401,0.00001427662],"genre_scores_gemma":[0.9910377,0.002395254,0.005609487,0.0002140689,0.0005811134,0.000004301368,0.00001408789,0.00001764908,0.0001263799],"genre_candidate":"empirical","genre_consensus":"empirical","teacher_disagreement_score":0.113689,"threshold_uncertainty_score":0.3939943,"prediction_status":"machine_predicted_unvalidated"},"labels":[],"label_agreement":null},{"id":"W2165008949","doi":"10.1136/jmg.2008.065904","title":"Natural course of Fabry disease: changing pattern of causes of death in FOS – Fabry Outcome Survey","year":2009,"lang":"en","type":"article","venue":"Journal of Medical Genetics","topic":"Lysosomal Storage Disorders Research","field":"Medicine","cited_by":306,"is_retracted":false,"has_abstract":true,"routes":{"ca_aff":true,"ca_fund":false,"ca_venue":false,"about_ca":false},"ca_institutions":"SickKids Foundation; Centre Hospitalier Universitaire de Sherbrooke; Hospital for Sick Children","funders":"","keywords":"Fabry disease; Medicine; Disease; Cause of death; Enzyme replacement therapy; Internal medicine; Cohort; Pediatrics","retraction":null,"screen_n_in":null,"score":{"opus":0.05598208530393117,"gpt":0.3902907356480986,"spread":0.3343086503441675,"validation_status":"score_only:v0-immature-baseline"},"prediction":{"model_version":"codex-gemma-dda1882f352a","candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.001796776,0.0001440582,0.0007587897,0.0003731107,0.00001370175,0.000003852522,0.0003744763,0.0001552425,0.0001268165],"category_scores_gemma":[0.00188828,0.0001060912,0.0002016456,0.0003942978,0.0001629313,0.00003716733,0.00008464118,0.0006128546,6.825591e-7],"about_ca_system_candidate":false,"about_ca_system_consensus":false,"about_ca_system_score_codex":0.00005822095,"about_ca_system_score_gemma":0.0005914583,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_topic_score_codex":0.00008009879,"about_ca_topic_score_gemma":0.00006392946,"domain_scores_codex":[0.9959158,0.0002013912,0.001138187,0.0001208557,0.002299899,0.0003238869],"domain_scores_gemma":[0.9979913,0.0002839453,0.0004997128,0.0002300711,0.0005495897,0.000445356],"domain_codex":null,"domain_gemma":null,"domain_candidate":null,"domain_consensus":null,"study_design_codex":"observational","study_design_gemma":"observational","study_design_scores_codex":[0.0003672554,0.0008006973,0.9424834,0.000325832,0.00009774721,0.0004291498,0.0003874513,0.00002248011,0.0009610024,0.000005821434,0.0001555143,0.05396364],"study_design_scores_gemma":[0.002594477,0.0006879586,0.9923129,0.0007391039,0.00008639377,0.00007156234,0.0003114523,0.001572166,0.001450733,0.00004684498,0.00003886488,0.00008751189],"study_design_candidate":"observational","study_design_consensus":"observational","genre_codex":"empirical","genre_gemma":"empirical","genre_scores_codex":[0.9863785,0.01054868,0.001196509,0.001487826,0.0001826047,0.0001554296,0.0000267609,0.000002660851,0.00002102509],"genre_scores_gemma":[0.9982414,0.001176073,0.000133075,0.0002456907,0.0001383726,5.856025e-7,0.000007904536,0.0000150532,0.00004189651],"genre_candidate":"empirical","genre_consensus":"empirical","teacher_disagreement_score":0.05387613,"threshold_uncertainty_score":0.4326274,"prediction_status":"machine_predicted_unvalidated"},"labels":[],"label_agreement":null},{"id":"W2157108110","doi":"10.1136/jmg.2010.077180","title":"<i>SOD1</i>, <i>ANG</i>, <i>VAPB</i>, <i>TARDBP</i>, and <i>FUS</i> mutations in familial amyotrophic lateral sclerosis: genotype–phenotype correlations","year":2010,"lang":"en","type":"article","venue":"Journal of Medical Genetics","topic":"Amyotrophic Lateral Sclerosis Research","field":"Medicine","cited_by":296,"is_retracted":false,"has_abstract":true,"routes":{"ca_aff":true,"ca_fund":false,"ca_venue":false,"about_ca":false},"ca_institutions":"Centre Hospitalier de l’Université de Montréal","funders":"Association pour la Recherche sur la Sclérose Latérale Amyotrophique et autres Maladies du Motoneurone","keywords":"TARDBP; Amyotrophic lateral sclerosis; Missense mutation; Genetics; Mutation; SOD1; Biology; Phenotype; Genotype; Gene; Medicine; Disease; Pathology","retraction":null,"screen_n_in":null,"score":{"opus":0.02499724181662158,"gpt":0.2952476937139239,"spread":0.2702504518973023,"validation_status":"score_only:v0-immature-baseline"},"prediction":{"model_version":"codex-gemma-dda1882f352a","candidate_categories":["metaepi_narrow","research_integrity"],"consensus_categories":[],"category_scores_codex":[0.00140336,0.0003338674,0.0007508607,0.0004211036,0.0001587337,0.00009049089,0.0004908732,0.0006176674,0.0005634371],"category_scores_gemma":[0.001040143,0.0002694118,0.0002176201,0.0006574251,0.0006447147,0.0001892574,0.0002249849,0.002892241,0.00004965645],"about_ca_system_candidate":false,"about_ca_system_consensus":false,"about_ca_system_score_codex":0.00009907008,"about_ca_system_score_gemma":0.0009501792,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_topic_score_codex":0.0001079462,"about_ca_topic_score_gemma":0.0002590684,"domain_scores_codex":[0.9948722,0.0001863006,0.001363951,0.0003809541,0.002508501,0.0006881679],"domain_scores_gemma":[0.9970852,0.0003067013,0.0003736769,0.0004334855,0.0005680178,0.001232897],"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":[0.001656446,0.002372385,0.3856897,0.0003579553,0.0005160229,0.001892054,0.002650582,0.0006218673,0.5190952,0.0009190234,0.009827683,0.07440105],"study_design_scores_gemma":[0.009637767,0.001412592,0.9652785,0.0006856237,0.0003204796,0.001637561,0.0001243434,0.003870048,0.001023932,0.001078843,0.01444685,0.0004834613],"study_design_candidate":"observational","study_design_consensus":null,"genre_codex":"empirical","genre_gemma":"empirical","genre_scores_codex":[0.9840071,0.001823491,0.000359054,0.01175887,0.00123074,0.0003884345,0.00001824465,0.00003054493,0.0003834975],"genre_scores_gemma":[0.9864861,0.004606318,0.004941015,0.002244819,0.001451785,0.00001214012,0.00001890281,0.00006724564,0.0001716512],"genre_candidate":"empirical","genre_consensus":"empirical","teacher_disagreement_score":0.5795888,"threshold_uncertainty_score":0.9999758,"prediction_status":"machine_predicted_unvalidated"},"labels":[],"label_agreement":null},{"id":"W1969426707","doi":"10.1136/jmg.40.3.153","title":"Nail patella syndrome: a review of the phenotype aided by developmental biology","year":2003,"lang":"en","type":"review","venue":"Journal of Medical Genetics","topic":"Renal Diseases and Glomerulopathies","field":"Medicine","cited_by":286,"is_retracted":false,"has_abstract":true,"routes":{"ca_aff":false,"ca_fund":true,"ca_venue":false,"about_ca":false},"ca_institutions":"","funders":"National Institutes of Health; Hospital for Sick Children; National Institute of Arthritis and Musculoskeletal and Skin Diseases; Johns Hopkins University","keywords":"Phenotype; Patella; Biology; Hypoplasia; Medicine; Pathology; Anatomy; Bioinformatics; Genetics; Gene","retraction":null,"screen_n_in":null,"score":{"opus":0.03690830595310492,"gpt":0.3532287028465904,"spread":0.3163203968934855,"validation_status":"score_only:v0-immature-baseline"},"prediction":{"model_version":"codex-gemma-dda1882f352a","candidate_categories":["insufficient_payload"],"consensus_categories":[],"category_scores_codex":[0.001113703,0.0003203121,0.002529778,0.00009796127,0.00003433434,0.000006269801,0.0005477795,0.000455387,0.000940678],"category_scores_gemma":[0.001318043,0.0001577336,0.001026265,0.0004085413,0.0002708391,0.00001055738,0.0001297846,0.0009007124,0.00002056197],"about_ca_system_candidate":false,"about_ca_system_consensus":false,"about_ca_system_score_codex":0.00009938466,"about_ca_system_score_gemma":0.00303052,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_topic_score_codex":0.000001641701,"about_ca_topic_score_gemma":2.575344e-7,"domain_scores_codex":[0.9957981,0.0004310964,0.001938017,0.0001745755,0.00140472,0.000253466],"domain_scores_gemma":[0.9974124,0.0001759245,0.001411459,0.000267551,0.0002516449,0.0004810482],"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":[0.000008630717,0.0001564391,0.00003400303,0.09996714,0.0004386682,0.0001791494,0.000008481562,9.530457e-9,0.000001714903,0.000008575479,0.03381915,0.865378],"study_design_scores_gemma":[0.0003414048,0.0002832333,0.00002502432,0.2009696,0.001917665,0.004865971,0.000007682779,2.43697e-7,0.000003356529,0.00002223477,0.7914467,0.0001168245],"study_design_candidate":"design_other","study_design_consensus":null,"genre_codex":"review","genre_gemma":"review","genre_scores_codex":[0.00009423662,0.9980244,0.00001427461,0.0005003847,0.0006493163,0.0003766866,0.00004128626,0.000002667923,0.000296724],"genre_scores_gemma":[0.00001582689,0.9977196,0.0003862469,0.00145731,0.0001603532,0.000005041431,0.00002313206,0.00003416841,0.0001982996],"genre_candidate":"review","genre_consensus":"review","teacher_disagreement_score":0.8652612,"threshold_uncertainty_score":0.9999726,"prediction_status":"machine_predicted_unvalidated"},"labels":[],"label_agreement":null},{"id":"W2143963530","doi":"10.1136/jmg.2006.042796","title":"The cardiofaciocutaneous syndrome","year":2006,"lang":"en","type":"review","venue":"Journal of Medical Genetics","topic":"Protein Tyrosine Phosphatases","field":"Biochemistry, Genetics and Molecular Biology","cited_by":270,"is_retracted":false,"has_abstract":true,"routes":{"ca_aff":true,"ca_fund":false,"ca_venue":false,"about_ca":false},"ca_institutions":"Children's Hospital of Eastern Ontario; University of Ottawa","funders":"","keywords":"Costello syndrome; PTPN11; Noonan syndrome; HRAS; Failure to thrive; Biology; Hypertelorism; KRAS; Cancer research; MAPK/ERK pathway; Mutation; Genetics; Medicine; Internal medicine; Kinase; Gene","retraction":null,"screen_n_in":null,"score":{"opus":0.01812208958461606,"gpt":0.3241717965936134,"spread":0.3060497070089973,"validation_status":"score_only:v0-immature-baseline"},"prediction":{"model_version":"codex-gemma-dda1882f352a","candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.001059057,0.0003177165,0.0009839567,0.00005040268,0.00009633743,0.0000612245,0.001451173,0.0006929245,0.00001802715],"category_scores_gemma":[0.0007685071,0.0001834313,0.0007838633,0.0001135608,0.0002336831,0.00000105209,0.0003113165,0.0006652215,0.00001544752],"about_ca_system_candidate":false,"about_ca_system_consensus":false,"about_ca_system_score_codex":0.00003628556,"about_ca_system_score_gemma":0.001208227,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_topic_score_codex":0.000002949152,"about_ca_topic_score_gemma":0.00000404411,"domain_scores_codex":[0.9968677,0.0002413778,0.001090818,0.0002069974,0.001269295,0.0003237754],"domain_scores_gemma":[0.9980836,0.0001215869,0.0008368854,0.0005226217,0.0001542293,0.0002810799],"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":[0.000007327717,0.0000266456,0.000001444731,0.0007575057,0.0003227468,0.0009042985,7.376856e-7,0.000005081644,0.000001977432,0.00003664771,0.03146156,0.9664741],"study_design_scores_gemma":[0.0001587083,0.000366018,0.000001333479,0.001621156,0.0004539574,0.01939395,0.000001876994,0.000001112147,0.0001017221,0.00003254639,0.9776773,0.0001903007],"study_design_candidate":"not_applicable","study_design_consensus":null,"genre_codex":"review","genre_gemma":"review","genre_scores_codex":[0.00002095756,0.998284,0.0003449955,0.0001303117,0.0008840956,0.0002090468,0.00005094272,0.000002980988,0.00007261433],"genre_scores_gemma":[0.00003827829,0.9977281,0.0003253237,0.00006203879,0.001409944,0.000008508458,0.00005589658,0.00005371015,0.0003182004],"genre_candidate":"review","genre_consensus":"review","teacher_disagreement_score":0.9662837,"threshold_uncertainty_score":0.7480109,"prediction_status":"machine_predicted_unvalidated"},"labels":[],"label_agreement":null},{"id":"W2118745131","doi":"10.1136/jmg.2008.062950","title":"Further clinical and molecular delineation of the 9q subtelomeric deletion syndrome supports a major contribution of <i>EHMT1</i> haploinsufficiency to the core phenotype","year":2009,"lang":"en","type":"article","venue":"Journal of Medical Genetics","topic":"Genomic variations and chromosomal abnormalities","field":"Biochemistry, Genetics and Molecular Biology","cited_by":258,"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","funders":"","keywords":"Haploinsufficiency; Genetics; Multiplex ligation-dependent probe amplification; Hypotonia; Biology; Phenotype; Mutation; Subtelomere; Gene; Exon; Telomere","retraction":null,"screen_n_in":null,"score":{"opus":0.009566302904239297,"gpt":0.2723113409223661,"spread":0.2627450380181268,"validation_status":"score_only:v0-immature-baseline"},"prediction":{"model_version":"codex-gemma-dda1882f352a","candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0009445046,0.00008432597,0.0001952678,0.00002865587,0.00004126181,0.000007476032,0.000260913,0.0001452606,0.00001833338],"category_scores_gemma":[0.0004134389,0.00005011901,0.0001185165,0.0001200202,0.0001302226,0.000002847404,0.00006370749,0.0001336799,5.552228e-7],"about_ca_system_candidate":false,"about_ca_system_consensus":false,"about_ca_system_score_codex":0.000007220732,"about_ca_system_score_gemma":0.000207239,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_topic_score_codex":0.00000479259,"about_ca_topic_score_gemma":0.000007320704,"domain_scores_codex":[0.9985137,0.000112211,0.0006929492,0.0001002875,0.0004618808,0.0001189616],"domain_scores_gemma":[0.9989306,0.00002431929,0.0004025352,0.000187903,0.0003526464,0.0001019644],"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":[0.00112145,0.002209674,0.1654769,0.0001365824,0.0006734752,0.00008172888,0.001701711,0.00781913,0.7271764,0.00304301,0.005004211,0.08555578],"study_design_scores_gemma":[0.005661063,0.01150084,0.7633969,0.0003693649,0.0007639921,0.002242309,0.0009762878,0.003188605,0.1810372,0.001918104,0.02836604,0.0005792102],"study_design_candidate":"observational","study_design_consensus":null,"genre_codex":"empirical","genre_gemma":"empirical","genre_scores_codex":[0.9795523,0.001696786,0.01539265,0.003028752,0.0001748671,0.0001323246,0.000009320967,0.000001001998,0.00001202741],"genre_scores_gemma":[0.9979172,0.0006064685,0.0005411519,0.0007641579,0.0001398012,9.820823e-7,0.000006915749,0.000005687691,0.00001764866],"genre_candidate":"empirical","genre_consensus":"empirical","teacher_disagreement_score":0.5979201,"threshold_uncertainty_score":0.2043794,"prediction_status":"machine_predicted_unvalidated"},"labels":[],"label_agreement":null},{"id":"W2013160042","doi":"10.1136/jmg.2006.041517","title":"<i>SMAD4</i> mutations found in unselected HHT patients","year":2006,"lang":"en","type":"article","venue":"Journal of Medical Genetics","topic":"Vascular Anomalies and Treatments","field":"Medicine","cited_by":256,"is_retracted":false,"has_abstract":true,"routes":{"ca_aff":true,"ca_fund":false,"ca_venue":false,"about_ca":false},"ca_institutions":"Toronto Western Hospital","funders":"National Heart, Lung, and Blood Institute; Instituto de Salud Carlos III; National Institutes of Health","keywords":"ACVRL1; Telangiectases; Endoglin; Telangiectasia; Medicine; Genetic testing; Mutation; Internal medicine; Gastroenterology; Genetics; Pathology; Gene; Biology","retraction":null,"screen_n_in":null,"score":{"opus":0.006892043634061029,"gpt":0.2657797109819259,"spread":0.2588876673478648,"validation_status":"score_only:v0-immature-baseline"},"prediction":{"model_version":"codex-gemma-dda1882f352a","candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0001778679,0.00008187648,0.0002281632,0.0001128015,0.00002434342,0.00001027978,0.00008402941,0.0001085513,0.0001381812],"category_scores_gemma":[0.0001464994,0.00006079957,0.0001015181,0.0002423514,0.0000462887,0.00002256174,0.00001511028,0.0002226607,0.0000105669],"about_ca_system_candidate":false,"about_ca_system_consensus":false,"about_ca_system_score_codex":0.00006610202,"about_ca_system_score_gemma":0.0002340314,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_topic_score_codex":0.00003639523,"about_ca_topic_score_gemma":0.00006885811,"domain_scores_codex":[0.9983088,0.00003661119,0.0004747033,0.00007285646,0.0009463078,0.0001607159],"domain_scores_gemma":[0.9993334,0.00004359771,0.0001323707,0.00008712165,0.0002183989,0.0001851256],"domain_codex":null,"domain_gemma":null,"domain_candidate":null,"domain_consensus":null,"study_design_codex":"observational","study_design_gemma":"observational","study_design_scores_codex":[0.0001117595,0.00231726,0.9746311,0.00004770436,0.0001948737,0.0009796631,0.000126215,0.000165259,0.00003645324,0.00008529258,0.004651467,0.01665296],"study_design_scores_gemma":[0.009638783,0.00085374,0.9690247,0.0002074369,0.0002263513,0.000393693,0.00003906287,0.0004171073,0.0003378582,0.0004636475,0.0183059,0.00009170432],"study_design_candidate":"observational","study_design_consensus":"observational","genre_codex":"empirical","genre_gemma":"empirical","genre_scores_codex":[0.9966457,0.001450903,0.0003373562,0.0005551169,0.0002002066,0.00009672149,0.000002373741,0.000004637929,0.0007069207],"genre_scores_gemma":[0.9979276,0.0000775724,0.001205293,0.00029925,0.0002488952,0.000001204086,0.00009151368,0.00001211265,0.0001365456],"genre_candidate":"empirical","genre_consensus":"empirical","teacher_disagreement_score":0.01656126,"threshold_uncertainty_score":0.2479335,"prediction_status":"machine_predicted_unvalidated"},"labels":[],"label_agreement":null},{"id":"W2604355298","doi":"10.1136/jmedgenet-2016-104509","title":"<i>GRIN2B</i> encephalopathy: novel findings on phenotype, variant clustering, functional consequences and treatment aspects","year":2017,"lang":"en","type":"article","venue":"Journal of Medical Genetics","topic":"Genomics and Rare Diseases","field":"Biochemistry, Genetics and Molecular Biology","cited_by":256,"is_retracted":false,"has_abstract":true,"routes":{"ca_aff":true,"ca_fund":false,"ca_venue":false,"about_ca":false},"ca_institutions":"McMaster Children's Hospital; Université de Montréal; McGill University; McMaster University; Montreal Children's Hospital","funders":"Eunice Kennedy Shriver National Institute of Child Health and Human Development; National Center for Advancing Translational Sciences; National Institute of Neurological Disorders and Stroke; Schweizerischer Nationalfonds zur Förderung der Wissenschaftlichen Forschung; National Health and Medical Research Council; Cure Kids; Wellcome Trust","keywords":"Phenotype; Biology; Computational biology; Encephalopathy; Bioinformatics; Genetics; Evolutionary biology; Medicine; Psychiatry; Gene","retraction":null,"screen_n_in":null,"score":{"opus":0.0249673423362159,"gpt":0.2737127594583202,"spread":0.2487454171221044,"validation_status":"score_only:v0-immature-baseline"},"prediction":{"model_version":"codex-gemma-dda1882f352a","candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0002209897,0.0001205538,0.0001532053,0.00002997629,0.000170885,0.00007605575,0.0002553271,0.0001288038,0.00004923955],"category_scores_gemma":[0.0002168323,0.00008691018,0.00007856991,0.00001115826,0.0002793858,0.000003360071,0.0001017355,0.00009336146,0.000002500091],"about_ca_system_candidate":false,"about_ca_system_consensus":false,"about_ca_system_score_codex":0.00001712336,"about_ca_system_score_gemma":0.0003592008,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_topic_score_codex":0.000006633704,"about_ca_topic_score_gemma":0.00003122997,"domain_scores_codex":[0.9990696,0.00001793181,0.0002329691,0.0001605859,0.0003735749,0.0001452842],"domain_scores_gemma":[0.9992352,0.00001775852,0.000204832,0.0001985306,0.00007353741,0.0002702115],"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":[0.003763768,0.004494071,0.0489214,0.0001859181,0.002455361,0.004765418,0.0008922249,0.002378436,0.7028922,0.009367364,0.01526857,0.2046153],"study_design_scores_gemma":[0.02323328,0.02010875,0.4872383,0.0007608969,0.0008099042,0.01161774,0.000627724,0.003699159,0.1159561,0.004084219,0.3299496,0.00191422],"study_design_candidate":"bench_or_experimental","study_design_consensus":null,"genre_codex":"empirical","genre_gemma":"empirical","genre_scores_codex":[0.9929993,0.001805413,0.001204645,0.002122341,0.0007092286,0.00006379249,0.00001905299,0.000001689228,0.001074592],"genre_scores_gemma":[0.9948293,0.003335892,0.000519982,0.0003964964,0.00080279,0.000001447786,0.000006101661,0.000009821819,0.00009816702],"genre_candidate":"empirical","genre_consensus":"empirical","teacher_disagreement_score":0.5869361,"threshold_uncertainty_score":0.3544094,"prediction_status":"machine_predicted_unvalidated"},"labels":[],"label_agreement":null},{"id":"W2144661178","doi":"10.1136/jmg.2004.027698","title":"Melanocortin-1 receptor gene variants affect pain and μ-opioid analgesia in mice and humans","year":2005,"lang":"en","type":"article","venue":"Journal of Medical Genetics","topic":"Regulation of Appetite and Obesity","field":"Neuroscience","cited_by":255,"is_retracted":false,"has_abstract":true,"routes":{"ca_aff":true,"ca_fund":true,"ca_venue":false,"about_ca":false},"ca_institutions":"McGill University","funders":"National Institute of Neurological Disorders and Stroke; National Institute on Drug Abuse; Canada Research Chairs; Children's Miracle Network Hospitals","keywords":"Opioid; μ-opioid receptor; Morphine; Melanocortin; Melanocortin 1 receptor; Analgesic; Opioid receptor; Pharmacogenetics; Pharmacology; Medicine; Receptor; Nociception; Genotype; Internal medicine; Biology; Endocrinology; Allele; Gene; Genetics","retraction":null,"screen_n_in":null,"score":{"opus":0.0180463517563162,"gpt":0.2787956066750193,"spread":0.2607492549187032,"validation_status":"score_only:v0-immature-baseline"},"prediction":{"model_version":"codex-gemma-dda1882f352a","candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.001689384,0.00009549718,0.0002057174,0.0001182718,0.000052796,0.00003699066,0.0001935021,0.0001242721,0.0001606509],"category_scores_gemma":[0.0009287497,0.00007736652,0.00003441705,0.0001301382,0.0001230826,0.00007256773,0.00005822265,0.0002731236,0.000004956873],"about_ca_system_candidate":false,"about_ca_system_consensus":false,"about_ca_system_score_codex":0.00002173556,"about_ca_system_score_gemma":0.00007715484,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_topic_score_codex":0.000002874506,"about_ca_topic_score_gemma":0.00001810006,"domain_scores_codex":[0.998269,0.0002857627,0.0004343686,0.0001574758,0.0006801953,0.0001731618],"domain_scores_gemma":[0.9990988,0.0003082855,0.0002035082,0.0000798391,0.00003084539,0.0002787082],"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":[0.0001697423,0.0004301853,0.06943365,0.00009085474,0.00002387782,0.0004154708,0.001368181,0.000159489,0.626065,0.0005287316,0.003728453,0.2975864],"study_design_scores_gemma":[0.00433007,0.001474053,0.6305174,0.0004040543,0.00005392681,0.0009639409,0.0001385469,0.01347979,0.2774254,0.00102923,0.069709,0.0004746295],"study_design_candidate":"bench_or_experimental","study_design_consensus":null,"genre_codex":"empirical","genre_gemma":"empirical","genre_scores_codex":[0.9945837,0.001078856,0.0009068964,0.003123657,0.0001099071,0.00006976655,0.000001544856,0.00000442765,0.0001212806],"genre_scores_gemma":[0.9905658,0.004878195,0.002772776,0.001271501,0.0004297384,5.257913e-7,3.207779e-7,0.000008691907,0.00007240443],"genre_candidate":"empirical","genre_consensus":"empirical","teacher_disagreement_score":0.5610837,"threshold_uncertainty_score":0.3154915,"prediction_status":"machine_predicted_unvalidated"},"labels":[],"label_agreement":null},{"id":"W1973405084","doi":"10.1136/jmg.39.4.251","title":"Long term health and neurodevelopment in children exposed to antiepileptic drugs before birth","year":2002,"lang":"en","type":"article","venue":"Journal of Medical Genetics","topic":"Pharmacological Effects and Toxicity Studies","field":"Medicine","cited_by":253,"is_retracted":false,"has_abstract":true,"routes":{"ca_aff":true,"ca_fund":true,"ca_venue":false,"about_ca":false},"ca_institutions":"Memorial University of Newfoundland","funders":"Memorial University of Newfoundland; University of Aberdeen","keywords":"Medicine; Pediatrics; Epilepsy; Retrospective cohort study; Antiepileptic drug; Pregnancy; In utero; Medical record; Population; Teratology; Congenital malformations; Global developmental delay; Fetus; Psychiatry; Surgery","retraction":null,"screen_n_in":null,"score":{"opus":0.02510654646018709,"gpt":0.3135815162354709,"spread":0.2884749697752839,"validation_status":"score_only:v0-immature-baseline"},"prediction":{"model_version":"codex-gemma-dda1882f352a","candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0005841703,0.0001211875,0.0004466036,0.0001506616,0.00004469323,0.00001135977,0.000122366,0.0000739244,0.0001355674],"category_scores_gemma":[0.0003227766,0.00007936482,0.00005041085,0.0001735284,0.00007584873,0.00001858463,0.000102502,0.0004374303,0.000004913831],"about_ca_system_candidate":false,"about_ca_system_consensus":false,"about_ca_system_score_codex":0.00005975542,"about_ca_system_score_gemma":0.0001060146,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_topic_score_codex":0.00000182966,"about_ca_topic_score_gemma":0.000003633581,"domain_scores_codex":[0.9981747,0.00007460908,0.0005274072,0.0001336738,0.0008169989,0.0002726152],"domain_scores_gemma":[0.9988006,0.00006189391,0.0001341179,0.00006788496,0.00004705868,0.0008884131],"domain_codex":null,"domain_gemma":null,"domain_candidate":null,"domain_consensus":null,"study_design_codex":"observational","study_design_gemma":"observational","study_design_scores_codex":[0.00007798395,0.00050467,0.6555696,0.0001098489,0.00009749345,0.0003606442,0.002130769,0.000005153011,0.0002375737,0.000003096096,0.003181447,0.3377217],"study_design_scores_gemma":[0.002943663,0.002807179,0.9918896,0.0003372524,0.00002451114,0.0005184219,0.00005988714,0.0002706016,0.0001728783,0.00001048382,0.0008850012,0.00008052935],"study_design_candidate":"observational","study_design_consensus":"observational","genre_codex":"empirical","genre_gemma":"empirical","genre_scores_codex":[0.9743058,0.00405072,0.00007704924,0.02111746,0.0001445455,0.0002577491,0.00000112054,0.000006441121,0.00003911115],"genre_scores_gemma":[0.9802466,0.00782056,0.0006803463,0.01092905,0.0002575116,0.000001826135,5.626304e-7,0.00000975581,0.00005379791],"genre_candidate":"empirical","genre_consensus":"empirical","teacher_disagreement_score":0.3376412,"threshold_uncertainty_score":0.3236404,"prediction_status":"machine_predicted_unvalidated"},"labels":[],"label_agreement":null},{"id":"W2902757858","doi":"10.1136/jmedgenet-2018-105625","title":"Kabuki syndrome: international consensus diagnostic criteria","year":2018,"lang":"en","type":"article","venue":"Journal of Medical Genetics","topic":"Genomics and Rare Diseases","field":"Biochemistry, Genetics and Molecular Biology","cited_by":248,"is_retracted":false,"has_abstract":true,"routes":{"ca_aff":true,"ca_fund":false,"ca_venue":false,"about_ca":false},"ca_institutions":"University of Manitoba","funders":"Eunice Kennedy Shriver National Institute of Child Health and Human Development","keywords":"Kabuki syndrome; Palpebral fissure; Medicine; Hypotonia; Dermatology; Genetic counseling; Intellectual disability; Genetic testing; Pediatrics; Genetics; Surgery; Biology; Psychiatry","retraction":null,"screen_n_in":null,"score":{"opus":0.01066148731641824,"gpt":0.302807591043505,"spread":0.2921461037270868,"validation_status":"score_only:v0-immature-baseline"},"prediction":{"model_version":"codex-gemma-dda1882f352a","candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0003315139,0.00009283316,0.0001313922,0.00004816177,0.00003800078,0.00002745752,0.000431088,0.0001491983,0.0005602242],"category_scores_gemma":[0.001343317,0.00007611674,0.0001034285,0.0000383372,0.0002059732,0.000001043535,0.0001330425,0.0001087258,0.00001959432],"about_ca_system_candidate":false,"about_ca_system_consensus":false,"about_ca_system_score_codex":0.00000988186,"about_ca_system_score_gemma":0.0002691892,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_topic_score_codex":0.000001540984,"about_ca_topic_score_gemma":0.00000434802,"domain_scores_codex":[0.99883,0.00004343217,0.0003570416,0.0001182555,0.0005015817,0.0001496887],"domain_scores_gemma":[0.9990236,0.0000507798,0.0001606464,0.0001446691,0.0003274638,0.0002928518],"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":[0.0008575864,0.001585012,0.03568816,0.0001039148,0.001716439,0.00675764,0.0003876819,0.00008579624,0.1914883,0.0002797232,0.6684641,0.09258569],"study_design_scores_gemma":[0.003584865,0.003465395,0.04065284,0.000336308,0.0001662378,0.01576937,0.0002478673,0.0006853467,0.02959597,0.000899926,0.9040721,0.0005237653],"study_design_candidate":"not_applicable","study_design_consensus":"not_applicable","genre_codex":"empirical","genre_gemma":"empirical","genre_scores_codex":[0.9915211,0.003074423,0.0007387177,0.002201102,0.002075529,0.00003889933,0.00001821707,0.000002127839,0.0003298946],"genre_scores_gemma":[0.9928266,0.00281743,0.001368222,0.0008346846,0.00203166,8.472269e-7,0.00001212392,0.00001356906,0.00009484095],"genre_candidate":"empirical","genre_consensus":"empirical","teacher_disagreement_score":0.235608,"threshold_uncertainty_score":0.6134062,"prediction_status":"machine_predicted_unvalidated"},"labels":[],"label_agreement":null},{"id":"W2049020090","doi":"10.1136/jmedgenet-2015-103018","title":"Rare variants in <i>SOS2</i> and <i>LZTR1</i> are associated with Noonan syndrome","year":2015,"lang":"en","type":"article","venue":"Journal of Medical Genetics","topic":"Protein Tyrosine Phosphatases","field":"Biochemistry, Genetics and Molecular Biology","cited_by":245,"is_retracted":false,"has_abstract":true,"routes":{"ca_aff":true,"ca_fund":false,"ca_venue":false,"about_ca":false},"ca_institutions":"McGill University","funders":"","keywords":"Noonan syndrome; Proband; Genetics; PTPN11; Missense mutation; Pedigree chart; Biology; Exome sequencing; Exome; Gene; Mutation; KRAS","retraction":null,"screen_n_in":null,"score":{"opus":0.01481811098303938,"gpt":0.2477166745522687,"spread":0.2328985635692293,"validation_status":"score_only:v0-immature-baseline"},"prediction":{"model_version":"codex-gemma-dda1882f352a","candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0008195564,0.0001362918,0.0002691955,0.00004981838,0.00001953718,0.00002486594,0.0002953184,0.0002319007,0.00001058372],"category_scores_gemma":[0.001206989,0.0001043316,0.00003524324,0.0001273801,0.0001249094,0.000006106933,0.0001363438,0.0002835966,0.000001198252],"about_ca_system_candidate":false,"about_ca_system_consensus":false,"about_ca_system_score_codex":0.00002766983,"about_ca_system_score_gemma":0.0004672142,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_topic_score_codex":0.000007628772,"about_ca_topic_score_gemma":0.00007316478,"domain_scores_codex":[0.9983927,0.0001022798,0.0003715873,0.0001595144,0.0007539398,0.0002199971],"domain_scores_gemma":[0.9988846,0.00002862242,0.0002998471,0.0001581439,0.0001944625,0.0004343475],"domain_codex":null,"domain_gemma":null,"domain_candidate":null,"domain_consensus":null,"study_design_codex":"observational","study_design_gemma":"observational","study_design_scores_codex":[0.002445838,0.002583317,0.8134924,0.0002485043,0.001078344,0.01798764,0.0005262209,0.0008057071,0.02965144,0.0003809533,0.1065425,0.02425711],"study_design_scores_gemma":[0.041309,0.01634182,0.5794619,0.004103788,0.0004493406,0.02137335,0.001141267,0.0006831502,0.2647648,0.002045526,0.06619252,0.002133548],"study_design_candidate":"observational","study_design_consensus":"observational","genre_codex":"empirical","genre_gemma":"empirical","genre_scores_codex":[0.9730953,0.02461201,0.0004406308,0.001511305,0.0001523017,0.00009547808,0.00002581757,0.000003250981,0.00006393393],"genre_scores_gemma":[0.9971471,0.001089105,0.0008839241,0.0006644101,0.0001407464,0.000002369299,0.00001803321,0.00002000155,0.0000343203],"genre_candidate":"empirical","genre_consensus":"empirical","teacher_disagreement_score":0.2351134,"threshold_uncertainty_score":0.4254521,"prediction_status":"machine_predicted_unvalidated"},"labels":[],"label_agreement":null},{"id":"W2113242315","doi":"10.1136/jmg.37.11.817","title":"Multiple endocrine neoplasia type 2 and<i>RET</i>: from neoplasia to neurogenesis","year":2000,"lang":"en","type":"review","venue":"Journal of Medical Genetics","topic":"Hedgehog Signaling Pathway Studies","field":"Biochemistry, Genetics and Molecular Biology","cited_by":241,"is_retracted":false,"has_abstract":true,"routes":{"ca_aff":true,"ca_fund":false,"ca_venue":false,"about_ca":false},"ca_institutions":"Queen's University","funders":"","keywords":"Multiple endocrine neoplasia type 2; Multiple endocrine neoplasia; Carcinogenesis; Proto-Oncogene Proteins c-ret; Cancer research; Germline mutation; Biology; Mutation; Cancer; Receptor tyrosine kinase; Medullary thyroid cancer; MEN1; Pheochromocytoma; Germline; Medullary carcinoma; Tyrosine kinase; Thyroid carcinoma; Genetics; Endocrinology; Gene; Thyroid cancer; Thyroid; Kinase; Signal transduction; Receptor","retraction":null,"screen_n_in":null,"score":{"opus":0.03621928832700033,"gpt":0.3347894568658241,"spread":0.2985701685388237,"validation_status":"score_only:v0-immature-baseline"},"prediction":{"model_version":"codex-gemma-dda1882f352a","candidate_categories":["metaepi_narrow"],"consensus_categories":[],"category_scores_codex":[0.0004550549,0.0004901731,0.001460554,0.0001531628,0.00006775461,0.00004246138,0.0007658939,0.0006304589,0.0001120056],"category_scores_gemma":[0.00203884,0.0003851958,0.0003694361,0.0002744404,0.0001184004,0.000002151539,0.000384741,0.0006207052,0.00004045691],"about_ca_system_candidate":false,"about_ca_system_consensus":false,"about_ca_system_score_codex":0.000024964,"about_ca_system_score_gemma":0.0009187843,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_topic_score_codex":0.000007704532,"about_ca_topic_score_gemma":0.00002674175,"domain_scores_codex":[0.9967882,0.0003126231,0.001144334,0.0004551334,0.0009019349,0.0003977969],"domain_scores_gemma":[0.9978421,0.0003056663,0.0004491064,0.0004180683,0.0002365394,0.0007484936],"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":[0.00006989134,0.00008446296,0.0001546007,0.0006505821,0.0005834689,0.0003803869,0.00005486458,0.00001422693,0.0004228018,8.606218e-7,0.008637575,0.9889463],"study_design_scores_gemma":[0.000474316,0.0006735798,0.00003130843,0.001732086,0.0006108337,0.0007976702,0.00001503053,0.00000965068,0.000500107,0.000004498185,0.9948265,0.0003244158],"study_design_candidate":"not_applicable","study_design_consensus":null,"genre_codex":"review","genre_gemma":"review","genre_scores_codex":[0.01306829,0.9852999,0.0001586217,0.0002230176,0.0008776116,0.000236618,0.00007882417,0.000007334578,0.00004972495],"genre_scores_gemma":[0.0004807535,0.9944794,0.001933367,0.0004938618,0.002338863,0.00000736658,0.00006111657,0.0000898791,0.0001153473],"genre_candidate":"review","genre_consensus":"review","teacher_disagreement_score":0.9886219,"threshold_uncertainty_score":0.99986,"prediction_status":"machine_predicted_unvalidated"},"labels":[],"label_agreement":null},{"id":"W2146683088","doi":"10.1136/jmg.2005.036657","title":"Mutation of <i>DNAJC19</i>, a human homologue of yeast inner mitochondrial membrane co-chaperones, causes DCMA syndrome, a novel autosomal recessive Barth syndrome-like condition","year":2005,"lang":"en","type":"article","venue":"Journal of Medical Genetics","topic":"Mitochondrial Function and Pathology","field":"Biochemistry, Genetics and Molecular Biology","cited_by":239,"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; University of Alberta; University of Calgary","funders":"Canadian Institutes of Health Research","keywords":"Biology; Genetics; Mutation; Inner membrane; Missense mutation; Gene; Mitochondrion","retraction":null,"screen_n_in":null,"score":{"opus":0.01421292713381148,"gpt":0.2839249284791645,"spread":0.2697120013453529,"validation_status":"score_only:v0-immature-baseline"},"prediction":{"model_version":"codex-gemma-dda1882f352a","candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0004024703,0.0002130804,0.0005381681,0.0001859203,0.00006211265,0.00001148572,0.0003481587,0.0005591689,0.0004569017],"category_scores_gemma":[0.0003079759,0.0001887043,0.0002133525,0.0001486068,0.0003577828,0.00001329034,0.00007245863,0.0003373857,0.000007212872],"about_ca_system_candidate":false,"about_ca_system_consensus":false,"about_ca_system_score_codex":0.00002448656,"about_ca_system_score_gemma":0.0003563413,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_topic_score_codex":0.00001438231,"about_ca_topic_score_gemma":0.0001183284,"domain_scores_codex":[0.9973738,0.0001866106,0.001116717,0.0002530945,0.0008272289,0.0002425234],"domain_scores_gemma":[0.998112,0.0000490034,0.0009227637,0.0002556812,0.0003973494,0.0002632485],"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":[0.0002965922,0.0004614184,0.000403945,0.0000792239,0.0001813007,0.0002055165,0.0002253612,0.000401047,0.9947432,0.00005027404,0.002209075,0.000743042],"study_design_scores_gemma":[0.01597656,0.01106809,0.02025645,0.0005967433,0.0006005813,0.03444868,0.0005623972,0.0003577799,0.8640404,0.0001274964,0.05114807,0.0008168077],"study_design_candidate":"bench_or_experimental","study_design_consensus":"bench_or_experimental","genre_codex":"empirical","genre_gemma":"empirical","genre_scores_codex":[0.991483,0.0007156099,0.005793804,0.0003850334,0.001203444,0.000184497,0.0001113542,0.000005779435,0.0001174821],"genre_scores_gemma":[0.9939588,0.0005173589,0.004045993,0.0003415933,0.0007063881,0.000006878921,0.0001884318,0.00002896546,0.0002056148],"genre_candidate":"empirical","genre_consensus":"empirical","teacher_disagreement_score":0.1307029,"threshold_uncertainty_score":0.769514,"prediction_status":"machine_predicted_unvalidated"},"labels":[],"label_agreement":null},{"id":"W2107403133","doi":"10.1136/jmedgenet-2015-103144","title":"The clinical application of genome-wide sequencing for monogenic diseases in Canada: Position Statement of the Canadian College of Medical Geneticists","year":2015,"lang":"en","type":"article","venue":"Journal of Medical Genetics","topic":"Genetics and Neurodevelopmental Disorders","field":"Biochemistry, Genetics and Molecular Biology","cited_by":234,"is_retracted":false,"has_abstract":true,"routes":{"ca_aff":true,"ca_fund":true,"ca_venue":false,"about_ca":true},"ca_institutions":"University Health Network; Dalhousie University; Centre Hospitalier Universitaire Sainte-Justine; University of Alberta; Memorial University of Newfoundland; SickKids Foundation; Western University; University of Toronto; University of Calgary; Mount Sinai Hospital; McGill University; Children's Hospital of Eastern Ontario; Université de Montréal; Hospital for Sick Children; University of British Columbia","funders":"Alberta Innovates; Hospital for Sick Children; Canadian Institutes of Health Research; Genome Canada; Ontario Genomics; Alberta Children's Hospital Research Institute; Ontario Genomics Institute","keywords":"Position statement; Genetics; Medical genetics; Statement (logic); Genome; Biology; Computational biology; Medicine; Family medicine; Political science; Gene; Law","retraction":null,"screen_n_in":null,"score":{"opus":0.0254079577417431,"gpt":0.3000961655985086,"spread":0.2746882078567655,"validation_status":"score_only:v0-immature-baseline"},"prediction":{"model_version":"codex-gemma-dda1882f352a","candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.001404067,0.00009520647,0.0002345194,0.00003977087,0.00004315393,0.000003303364,0.0006517009,0.0001439215,0.000004174879],"category_scores_gemma":[0.0008449452,0.00006413204,0.0001119871,0.0001130913,0.0002000468,0.000001428506,0.0001120744,0.0001284329,5.988333e-8],"about_ca_system_candidate":true,"about_ca_system_consensus":false,"about_ca_system_score_codex":0.0001981027,"about_ca_system_score_gemma":0.01569652,"about_ca_topic_candidate":true,"about_ca_topic_consensus":true,"about_ca_topic_score_codex":0.06752077,"about_ca_topic_score_gemma":0.8843368,"domain_scores_codex":[0.9971611,0.0001483383,0.001153889,0.000124156,0.001216786,0.0001956842],"domain_scores_gemma":[0.9983826,0.00009894965,0.0005421225,0.000211454,0.0003463107,0.0004185758],"domain_codex":null,"domain_gemma":null,"domain_candidate":null,"domain_consensus":null,"study_design_codex":"observational","study_design_gemma":"observational","study_design_scores_codex":[0.001153814,0.0008466739,0.8550731,0.0004567526,0.0008992547,0.00005717935,0.0005353757,0.01365268,0.05575818,0.0003814556,0.02414949,0.04703603],"study_design_scores_gemma":[0.005053716,0.001536682,0.8991061,0.0001943499,0.0001900564,0.00006991832,0.001574655,0.007551598,0.04828589,0.0009520472,0.03515853,0.0003264247],"study_design_candidate":"observational","study_design_consensus":"observational","genre_codex":"empirical","genre_gemma":"empirical","genre_scores_codex":[0.9921966,0.003205294,0.001016764,0.00290019,0.0002663701,0.0002892727,0.000111961,2.748147e-7,0.00001325502],"genre_scores_gemma":[0.9967389,0.00244899,0.0003821366,0.0003437902,0.00004878849,0.000007275475,0.00001343955,0.00001091145,0.000005843515],"genre_candidate":"empirical","genre_consensus":"empirical","teacher_disagreement_score":0.816816,"threshold_uncertainty_score":0.9898835,"prediction_status":"machine_predicted_unvalidated"},"labels":[],"label_agreement":null},{"id":"W2165213798","doi":"10.1136/jmedgenet-2011-100544","title":"<i>NOTCH2</i> mutations in Alagille syndrome","year":2011,"lang":"en","type":"article","venue":"Journal of Medical Genetics","topic":"Pediatric Hepatobiliary Diseases and Treatments","field":"Medicine","cited_by":219,"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":"National Institute of Diabetes and Digestive and Kidney Diseases","keywords":"JAG1; Alagille syndrome; Missense mutation; Penetrance; Notch signaling pathway; Mutation; Biology; Genetics; Cancer research; Phenotype; Endocrinology; Receptor; Cholestasis; Gene","retraction":null,"screen_n_in":null,"score":{"opus":0.03333715205084196,"gpt":0.2983026869135776,"spread":0.2649655348627357,"validation_status":"score_only:v0-immature-baseline"},"prediction":{"model_version":"codex-gemma-dda1882f352a","candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0002963204,0.00008004792,0.0002538325,0.000136495,0.0000158081,0.000003495203,0.0001221095,0.0001093042,0.0006868324],"category_scores_gemma":[0.0002164087,0.00005839495,0.000118032,0.0001816924,0.0000529828,0.00003169945,0.00002734048,0.0002416734,0.00002901505],"about_ca_system_candidate":false,"about_ca_system_consensus":false,"about_ca_system_score_codex":0.00004449337,"about_ca_system_score_gemma":0.0004583215,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_topic_score_codex":0.00002717652,"about_ca_topic_score_gemma":0.000006833923,"domain_scores_codex":[0.9984663,0.00003891234,0.0004775178,0.00007856717,0.0007772391,0.0001614958],"domain_scores_gemma":[0.9990828,0.00004769483,0.0001248889,0.0001151421,0.0000825274,0.0005469477],"domain_codex":null,"domain_gemma":null,"domain_candidate":null,"domain_consensus":null,"study_design_codex":"observational","study_design_gemma":"observational","study_design_scores_codex":[0.0001217685,0.002096344,0.955892,0.00005707408,0.0001565217,0.01612698,0.0003386854,0.000004560086,0.0000219,0.00004272485,0.002070893,0.02307059],"study_design_scores_gemma":[0.005918852,0.001504803,0.9791516,0.0002361592,0.0004937069,0.006026955,0.0001853368,0.0003317407,0.0001903996,0.0009846064,0.004845751,0.0001300806],"study_design_candidate":"observational","study_design_consensus":"observational","genre_codex":"empirical","genre_gemma":"empirical","genre_scores_codex":[0.9949711,0.002213581,0.0001235465,0.0009113197,0.0002177123,0.00008343847,0.000004046453,0.000005127184,0.001470127],"genre_scores_gemma":[0.9952878,0.002295341,0.0017435,0.0004586166,0.0001284427,0.000001873557,0.000002847271,0.00001015512,0.00007146441],"genre_candidate":"empirical","genre_consensus":"empirical","teacher_disagreement_score":0.02325965,"threshold_uncertainty_score":0.7520332,"prediction_status":"machine_predicted_unvalidated"},"labels":[],"label_agreement":null},{"id":"W2162805839","doi":"10.1136/jmg.2008.058701","title":"Clinical and molecular delineation of the 17q21.31 microdeletion syndrome","year":2008,"lang":"en","type":"article","venue":"Journal of Medical Genetics","topic":"Genomic variations and chromosomal abnormalities","field":"Biochemistry, Genetics and Molecular Biology","cited_by":217,"is_retracted":false,"has_abstract":true,"routes":{"ca_aff":true,"ca_fund":false,"ca_venue":false,"about_ca":false},"ca_institutions":"McMaster University; McMaster University Medical Centre","funders":"Eunice Kennedy Shriver National Institute of Child Health and Human Development; Howard Hughes Medical Institute","keywords":"Breakpoint; Genetics; Hypotonia; Comparative genomic hybridization; Microdeletion syndrome; Copy-number variation; Biology; Craniofacial; Disease gene identification; Gene; Chromosome; Phenotype; Genome; Exome sequencing","retraction":null,"screen_n_in":null,"score":{"opus":0.01427083062253857,"gpt":0.2692331538222746,"spread":0.254962323199736,"validation_status":"score_only:v0-immature-baseline"},"prediction":{"model_version":"codex-gemma-dda1882f352a","candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0004982692,0.00006600937,0.0001473343,0.00002175887,0.00004426171,0.000004413997,0.0002083799,0.0001729952,0.0000144755],"category_scores_gemma":[0.0002086502,0.00004546099,0.0001179089,0.00004622062,0.0002123974,0.000002014917,0.00009305141,0.0001427347,5.613373e-7],"about_ca_system_candidate":false,"about_ca_system_consensus":false,"about_ca_system_score_codex":0.000003649813,"about_ca_system_score_gemma":0.0002444797,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_topic_score_codex":0.000002994184,"about_ca_topic_score_gemma":0.000002145643,"domain_scores_codex":[0.9988476,0.00009155823,0.0005441144,0.00008180273,0.0003514305,0.00008351313],"domain_scores_gemma":[0.9993154,0.00001543477,0.0002564784,0.0001395116,0.0001785719,0.00009457035],"domain_codex":null,"domain_gemma":null,"domain_candidate":null,"domain_consensus":null,"study_design_codex":"observational","study_design_gemma":"observational","study_design_scores_codex":[0.0002234541,0.0007145436,0.5516648,0.0001436615,0.0006006886,0.0001943521,0.0004814788,0.000934805,0.4177144,0.0006331721,0.008380376,0.01831425],"study_design_scores_gemma":[0.005485863,0.00305328,0.6006058,0.0002746308,0.000344535,0.01709138,0.0004177342,0.001506444,0.2923777,0.0008309334,0.07748145,0.0005302625],"study_design_candidate":"observational","study_design_consensus":"observational","genre_codex":"empirical","genre_gemma":"empirical","genre_scores_codex":[0.9903901,0.002090616,0.006472749,0.0007308197,0.0002335507,0.00004515245,0.000003873459,7.662326e-7,0.00003235237],"genre_scores_gemma":[0.9938412,0.003611129,0.001957035,0.0003022296,0.0001946856,5.308597e-7,0.000003263649,0.000006457017,0.00008344009],"genre_candidate":"empirical","genre_consensus":"empirical","teacher_disagreement_score":0.1253368,"threshold_uncertainty_score":0.1853845,"prediction_status":"machine_predicted_unvalidated"},"labels":[],"label_agreement":null},{"id":"W2476341356","doi":"10.1136/jmedgenet-2016-103839","title":"<i>PALB2</i>, <i>CHEK2</i> and <i>ATM</i> rare variants and cancer risk: data from COGS","year":2016,"lang":"en","type":"article","venue":"Journal of Medical Genetics","topic":"BRCA gene mutations in cancer","field":"Biochemistry, Genetics and Molecular Biology","cited_by":217,"is_retracted":false,"has_abstract":true,"routes":{"ca_aff":true,"ca_fund":true,"ca_venue":false,"about_ca":false},"ca_institutions":"Canada's Michael Smith Genome Sciences Centre; Université Laval; BC Cancer Agency; Women's College Hospital; Centre hospitalier universitaire de Québec; Simon Fraser University; McGill University Health Centre; McGill University; McGill University and Génome Québec Innovation Centre; Public Health Ontario; University Health Network; University of Toronto; Mount Sinai Hospital; Lunenfeld-Tanenbaum Research Institute","funders":"National Cancer Institute; Medical Research Council; Canadian Institutes of Health Research; Deutsche Krebshilfe; National Institute for Health and Care Research; National Health and Medical Research Council; Cancer Research UK; Francis Crick Institute; Wellcome Trust; National Center for Research Resources; Génome Québec; Susan G. Komen; Memorial Sloan-Kettering Cancer Center; National Institutes of Health; Ovarian Cancer Research Fund; Breast Cancer Research Foundation; U.S. Department of Defense; McGill University; Royal Marsden NHS Foundation Trust","keywords":"CHEK2; PALB2; Genetics; Cancer; Biology; Mutation; Gene; Germline mutation","retraction":null,"screen_n_in":null,"score":{"opus":0.02272818808327409,"gpt":0.3091979531176691,"spread":0.286469765034395,"validation_status":"score_only:v0-immature-baseline"},"prediction":{"model_version":"codex-gemma-dda1882f352a","candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0006394974,0.0001464187,0.0002176014,0.00003072618,0.0000599873,0.00003067505,0.0005721483,0.0002614149,0.0001464188],"category_scores_gemma":[0.000469176,0.00009861082,0.00003700402,0.00005516069,0.0002567554,0.000009947119,0.0005080752,0.000193222,0.00000219761],"about_ca_system_candidate":false,"about_ca_system_consensus":false,"about_ca_system_score_codex":0.00002143631,"about_ca_system_score_gemma":0.0004407967,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_topic_score_codex":0.00003696599,"about_ca_topic_score_gemma":0.0001053055,"domain_scores_codex":[0.998412,0.0001091431,0.0004187864,0.0003178314,0.0005493817,0.0001928714],"domain_scores_gemma":[0.9986618,0.0001067259,0.0003071963,0.0004497757,0.0001429808,0.0003315134],"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":[0.0002375744,0.0001123759,0.07673943,0.00003083848,0.0005728971,0.000071332,0.0001343741,0.000009476592,0.09832388,0.000009035393,0.1309696,0.6927892],"study_design_scores_gemma":[0.007442012,0.0005266124,0.05783982,0.0003927172,0.0005403284,0.0005171645,0.0001564398,0.0004965197,0.05508128,0.000857153,0.8755637,0.0005862085],"study_design_candidate":"not_applicable","study_design_consensus":null,"genre_codex":"empirical","genre_gemma":"empirical","genre_scores_codex":[0.9296215,0.05522953,0.008667726,0.004862403,0.0007438297,0.00009457386,0.0006930664,0.000003756067,0.00008361923],"genre_scores_gemma":[0.8356732,0.1567622,0.00415061,0.001474983,0.001746977,0.00000529941,0.00002680727,0.00003199061,0.0001279826],"genre_candidate":"empirical","genre_consensus":"empirical","teacher_disagreement_score":0.7445942,"threshold_uncertainty_score":0.4021233,"prediction_status":"machine_predicted_unvalidated"},"labels":[],"label_agreement":null},{"id":"W2057343637","doi":"10.1136/jmg.2004.027730","title":"Rett syndrome: clinical review and genetic update","year":2005,"lang":"en","type":"review","venue":"Journal of Medical Genetics","topic":"Genetics and Neurodevelopmental Disorders","field":"Biochemistry, Genetics and Molecular Biology","cited_by":213,"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":"Rett syndrome; MECP2; Neurodevelopmental disorder; Biology; Phenotype; Mutation; Genetics; Intellectual disability; Repressor; Gene; Xenopus; Neuroscience; Gene expression","retraction":null,"screen_n_in":null,"score":{"opus":0.04158685686900118,"gpt":0.3848466867864292,"spread":0.343259829917428,"validation_status":"score_only:v0-immature-baseline"},"prediction":{"model_version":"codex-gemma-dda1882f352a","candidate_categories":["metaepi_narrow"],"consensus_categories":[],"category_scores_codex":[0.00119899,0.0004727742,0.001903599,0.000106179,0.00004856796,0.00003308221,0.0009762957,0.0008909443,0.0001741647],"category_scores_gemma":[0.0005234346,0.0003644773,0.0006821641,0.0001618953,0.0002556772,0.000002217725,0.0005015825,0.0008978387,0.00002864582],"about_ca_system_candidate":false,"about_ca_system_consensus":false,"about_ca_system_score_codex":0.00001725277,"about_ca_system_score_gemma":0.001070556,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_topic_score_codex":3.374096e-7,"about_ca_topic_score_gemma":0.000003111056,"domain_scores_codex":[0.9955341,0.0004078127,0.00229896,0.0004734697,0.0009289681,0.0003566813],"domain_scores_gemma":[0.9975361,0.00005327867,0.001100378,0.000461123,0.0001511686,0.0006979163],"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":[0.00000421867,0.00008934613,0.00002626405,0.005255008,0.0003042513,0.0001995011,0.000001533247,4.046233e-7,0.000001828293,0.000001315417,0.02469828,0.969418],"study_design_scores_gemma":[0.0003953413,0.0005085364,0.0003145017,0.007909246,0.001516844,0.007208407,0.000001909364,0.000001754216,0.000001403816,0.000008271751,0.9817725,0.0003612738],"study_design_candidate":"not_applicable","study_design_consensus":null,"genre_codex":"review","genre_gemma":"review","genre_scores_codex":[0.0005515171,0.9976107,0.00009399978,0.0007463339,0.000574427,0.0003510531,0.000017413,0.000003238156,0.00005127735],"genre_scores_gemma":[0.00003972498,0.9942228,0.002463027,0.002611205,0.0003955037,0.000007661737,0.00003958402,0.00008100305,0.0001395415],"genre_candidate":"review","genre_consensus":"review","teacher_disagreement_score":0.9690568,"threshold_uncertainty_score":0.9998807,"prediction_status":"machine_predicted_unvalidated"},"labels":[],"label_agreement":null},{"id":"W2108989136","doi":"10.1136/jmg.2005.033571","title":"Androgenetic/biparental mosaicism causes placental mesenchymal dysplasia","year":2005,"lang":"en","type":"letter","venue":"Journal of Medical Genetics","topic":"Gestational Trophoblastic Disease Studies","field":"Medicine","cited_by":197,"is_retracted":false,"has_abstract":true,"routes":{"ca_aff":true,"ca_fund":false,"ca_venue":false,"about_ca":false},"ca_institutions":"Victoria General Hospital; University of British Columbia","funders":"","keywords":"Beckwith–Wiedemann syndrome; Trophoblast; Biology; Uniparental disomy; Intrauterine growth restriction; Aneuploidy; Placenta; Fetus; Genetics; Karyotype; Pregnancy; Chromosome; DNA methylation","retraction":null,"screen_n_in":null,"score":{"opus":0.02282274408639705,"gpt":0.3080165307499646,"spread":0.2851937866635675,"validation_status":"score_only:v0-immature-baseline"},"prediction":{"model_version":"codex-gemma-dda1882f352a","candidate_categories":["metaepi_narrow","research_integrity","insufficient_payload"],"consensus_categories":[],"category_scores_codex":[0.000369354,0.0005266542,0.001157369,0.0003481115,0.0000842123,0.0000438221,0.0005141619,0.001019378,0.001743639],"category_scores_gemma":[0.0008878966,0.0004121536,0.000514155,0.0001791004,0.0004949833,0.00003999663,0.0001987176,0.002988218,0.0001704134],"about_ca_system_candidate":false,"about_ca_system_consensus":false,"about_ca_system_score_codex":0.0002618108,"about_ca_system_score_gemma":0.001904935,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_topic_score_codex":0.00000314031,"about_ca_topic_score_gemma":0.000005071429,"domain_scores_codex":[0.9916328,0.0001341885,0.001406531,0.0003503198,0.005863678,0.0006124699],"domain_scores_gemma":[0.9971699,0.0004063161,0.0007424926,0.0002983687,0.0005531326,0.0008298515],"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":[0.0001856416,0.0003071709,0.002200732,0.0002997622,0.0009736762,0.01435333,0.0001207445,0.0000343385,0.00006461837,0.000005157397,0.9795664,0.001888461],"study_design_scores_gemma":[0.004811479,0.001433918,0.009887364,0.0014724,0.002113587,0.01394559,0.0002476383,0.0002788527,0.0002487318,0.00008134246,0.9649937,0.0004854108],"study_design_candidate":"not_applicable","study_design_consensus":"not_applicable","genre_codex":"commentary","genre_gemma":"commentary","genre_scores_codex":[0.1578165,0.02220793,0.0002222608,0.8140183,0.003679476,0.0005233363,0.0003163395,0.00003993339,0.001175904],"genre_scores_gemma":[0.104685,0.02230482,0.01150783,0.7806846,0.07421412,0.00002728587,0.0008524121,0.0004147812,0.005309116],"genre_candidate":"commentary","genre_consensus":"commentary","teacher_disagreement_score":0.07053465,"threshold_uncertainty_score":0.999833,"prediction_status":"machine_predicted_unvalidated"},"labels":[],"label_agreement":null},{"id":"W2142952274","doi":"10.1136/jmedgenet-2013-101567","title":"Mutations in WNT1 are a cause of osteogenesis imperfecta","year":2013,"lang":"en","type":"article","venue":"Journal of Medical Genetics","topic":"Connective tissue disorders research","field":"Biochemistry, Genetics and Molecular Biology","cited_by":196,"is_retracted":false,"has_abstract":true,"routes":{"ca_aff":true,"ca_fund":true,"ca_venue":false,"about_ca":false},"ca_institutions":"Montreal Children's Hospital; McGill University and Génome Québec Innovation Centre; McGill University","funders":"McGill University","keywords":"Osteogenesis imperfecta; Medicine; Mutation; Genetics; Bioinformatics; Orthodontics; Biology; Anatomy; Gene","retraction":null,"screen_n_in":null,"score":{"opus":0.01974063964537321,"gpt":0.3302492828667016,"spread":0.3105086432213284,"validation_status":"score_only:v0-immature-baseline"},"prediction":{"model_version":"codex-gemma-dda1882f352a","candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.000417243,0.00008012036,0.0001880103,0.0001233868,0.00001592953,0.000009372832,0.0003191415,0.0001637659,0.0004217721],"category_scores_gemma":[0.001192103,0.00006867704,0.00008555145,0.0001607927,0.0001147329,0.000002903879,0.0001058492,0.0001775515,0.000006615619],"about_ca_system_candidate":false,"about_ca_system_consensus":false,"about_ca_system_score_codex":0.00001482823,"about_ca_system_score_gemma":0.0002923438,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_topic_score_codex":0.00005824462,"about_ca_topic_score_gemma":0.0001230061,"domain_scores_codex":[0.9985957,0.0001171691,0.0004083292,0.0001072108,0.0005980266,0.000173531],"domain_scores_gemma":[0.9990683,0.00005987862,0.0001828187,0.0001599882,0.0003476462,0.0001813548],"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":[0.0001150428,0.0006107289,0.3046642,0.0001163616,0.0002677088,0.0001270153,0.0004504652,0.0003110652,0.6166986,0.00002888444,0.006346685,0.07026324],"study_design_scores_gemma":[0.006065109,0.002968692,0.5716284,0.0003453408,0.0001072566,0.0005371835,0.004222056,0.001389864,0.3992962,0.0007972359,0.01213022,0.0005124134],"study_design_candidate":"bench_or_experimental","study_design_consensus":null,"genre_codex":"empirical","genre_gemma":"empirical","genre_scores_codex":[0.9936854,0.004205077,0.0004357335,0.001375492,0.00007486949,0.0001217979,0.000004746787,8.009017e-7,0.00009606078],"genre_scores_gemma":[0.9976245,0.001731724,0.0003361611,0.00009827739,0.0001251212,0.000006435021,0.000004417841,0.0000124569,0.00006088207],"genre_candidate":"empirical","genre_consensus":"empirical","teacher_disagreement_score":0.2669642,"threshold_uncertainty_score":0.4618109,"prediction_status":"machine_predicted_unvalidated"},"labels":[],"label_agreement":null},{"id":"W2157150055","doi":"10.1136/jmg.2008.062463","title":"Contribution of <i>TARDBP</i> mutations to sporadic amyotrophic lateral sclerosis","year":2008,"lang":"en","type":"article","venue":"Journal of Medical Genetics","topic":"Amyotrophic Lateral Sclerosis Research","field":"Medicine","cited_by":191,"is_retracted":false,"has_abstract":true,"routes":{"ca_aff":true,"ca_fund":false,"ca_venue":false,"about_ca":false},"ca_institutions":"Université Laval; Hôpital de l'Enfant-Jésus; Université de Montréal","funders":"","keywords":"TARDBP; Amyotrophic lateral sclerosis; Genetics; Missense mutation; Mutation; Gene; Biology; Gene mutation; Medicine; Pathology; Disease; Mutant; SOD1","retraction":null,"screen_n_in":null,"score":{"opus":0.0505321316793452,"gpt":0.3206585518400143,"spread":0.2701264201606691,"validation_status":"score_only:v0-immature-baseline"},"prediction":{"model_version":"codex-gemma-dda1882f352a","candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0008018228,0.0001418652,0.0005730462,0.0002665477,0.00007768693,0.000009590725,0.0003154086,0.0002231281,0.0005661838],"category_scores_gemma":[0.001106333,0.0001058527,0.0002242566,0.0004778442,0.0003116289,0.00005690452,0.00008638712,0.0005976205,0.00003507371],"about_ca_system_candidate":false,"about_ca_system_consensus":false,"about_ca_system_score_codex":0.0001374719,"about_ca_system_score_gemma":0.0006832326,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_topic_score_codex":0.00002587371,"about_ca_topic_score_gemma":0.000003598074,"domain_scores_codex":[0.9956645,0.0001102252,0.0009816274,0.0001473537,0.002743588,0.0003527445],"domain_scores_gemma":[0.9973179,0.0001074405,0.0002969188,0.0002281905,0.00102767,0.001021954],"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":[0.00362358,0.003280792,0.378108,0.0003417799,0.001219706,0.004535248,0.003272497,0.001617994,0.5176389,0.0004427883,0.04144693,0.04447182],"study_design_scores_gemma":[0.005500087,0.002958116,0.9691531,0.0008276143,0.0001743817,0.002178147,0.00003675713,0.0009330625,0.01240933,0.0001900356,0.005461288,0.0001780545],"study_design_candidate":"observational","study_design_consensus":null,"genre_codex":"empirical","genre_gemma":"empirical","genre_scores_codex":[0.9837884,0.0008335049,0.001965735,0.01285606,0.0002601364,0.0002233344,0.000008524865,0.000009839481,0.00005445193],"genre_scores_gemma":[0.9925464,0.002967446,0.002792254,0.0009732477,0.000599476,0.00000313816,0.000008028886,0.00002177096,0.00008824278],"genre_candidate":"empirical","genre_consensus":"empirical","teacher_disagreement_score":0.5910451,"threshold_uncertainty_score":0.6199315,"prediction_status":"machine_predicted_unvalidated"},"labels":[],"label_agreement":null},{"id":"W2142039491","doi":"10.1136/jmg.40.7.473","title":"Mutations at the <i>SALL4</i> locus on chromosome 20 result in a range of clinically overlapping phenotypes, including Okihiro syndrome, Holt-Oram syndrome, acro-renal-ocular syndrome, and patients previously reported to represent thalidomide embryopathy","year":2003,"lang":"en","type":"article","venue":"Journal of Medical Genetics","topic":"Renal and related cancers","field":"Biochemistry, Genetics and Molecular Biology","cited_by":188,"is_retracted":false,"has_abstract":true,"routes":{"ca_aff":false,"ca_fund":true,"ca_venue":false,"about_ca":false},"ca_institutions":"","funders":"Hospital for Sick Children","keywords":"Locus (genetics); Genetics; Phenotype; Medicine; Missense mutation; Biology; Gene","retraction":null,"screen_n_in":null,"score":{"opus":0.01661889395697885,"gpt":0.2926574417306202,"spread":0.2760385477736413,"validation_status":"score_only:v0-immature-baseline"},"prediction":{"model_version":"codex-gemma-dda1882f352a","candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.002236441,0.0002788758,0.0006302834,0.0001538843,0.0001202483,0.00003048159,0.0004605302,0.0004510232,0.00002989722],"category_scores_gemma":[0.002579962,0.000193613,0.0002382913,0.0004121293,0.0002619606,0.000009945762,0.0002749963,0.0006292789,0.000004019869],"about_ca_system_candidate":false,"about_ca_system_consensus":false,"about_ca_system_score_codex":0.0000997649,"about_ca_system_score_gemma":0.0003839605,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_topic_score_codex":0.00002096075,"about_ca_topic_score_gemma":0.0000299166,"domain_scores_codex":[0.9955103,0.0004015039,0.001929829,0.0004507434,0.001288991,0.0004186185],"domain_scores_gemma":[0.9974808,0.0001793866,0.00106916,0.0005188274,0.000280492,0.0004714047],"domain_codex":null,"domain_gemma":null,"domain_candidate":null,"domain_consensus":null,"study_design_codex":"observational","study_design_gemma":"observational","study_design_scores_codex":[0.009553958,0.007772697,0.43683,0.001835734,0.008665438,0.0348454,0.004812052,0.08547188,0.3484554,0.0001331517,0.0336363,0.02798798],"study_design_scores_gemma":[0.0820737,0.05782112,0.4230539,0.02186594,0.00375823,0.1140572,0.002014046,0.001295975,0.1144506,0.001595654,0.1718799,0.006133791],"study_design_candidate":"observational","study_design_consensus":"observational","genre_codex":"empirical","genre_gemma":"empirical","genre_scores_codex":[0.9924261,0.005561253,0.0001797081,0.0006481539,0.0004024798,0.0004686193,0.00002085813,0.00000456191,0.0002882938],"genre_scores_gemma":[0.9942349,0.004381093,0.000427538,0.0005777618,0.00006995808,0.0000144139,0.00002238232,0.00003804311,0.0002338817],"genre_candidate":"empirical","genre_consensus":"empirical","teacher_disagreement_score":0.2340048,"threshold_uncertainty_score":0.7895309,"prediction_status":"machine_predicted_unvalidated"},"labels":[],"label_agreement":null},{"id":"W2095324296","doi":"10.1136/jmg.2007.051268","title":"Germline E-cadherin mutations in familial lobular breast cancer","year":2007,"lang":"en","type":"letter","venue":"Journal of Medical Genetics","topic":"BRCA gene mutations in cancer","field":"Biochemistry, Genetics and Molecular Biology","cited_by":187,"is_retracted":false,"has_abstract":true,"routes":{"ca_aff":true,"ca_fund":false,"ca_venue":false,"about_ca":false},"ca_institutions":"BC Cancer Agency; University of British Columbia","funders":"Charles A. King Trust; Commonwealth of Massachusetts; Breast Cancer Research Foundation","keywords":"Cadherin; Germline; Germline mutation; Breast cancer; Genetics; Mutation; Medicine; Cancer; Biology; Cancer research; Oncology; Gene; Cell","retraction":null,"screen_n_in":null,"score":{"opus":0.01648949947407916,"gpt":0.3192863961755218,"spread":0.3027968967014427,"validation_status":"score_only:v0-immature-baseline"},"prediction":{"model_version":"codex-gemma-dda1882f352a","candidate_categories":["metaepi_narrow","research_integrity"],"consensus_categories":[],"category_scores_codex":[0.0008526499,0.0003043295,0.0004461853,0.0002815657,0.00003752002,0.00002838442,0.0008168292,0.001829209,0.000457075],"category_scores_gemma":[0.0002049916,0.0002825642,0.0002494911,0.0002510234,0.0002572928,0.000003385159,0.0001471132,0.002137474,0.000009127608],"about_ca_system_candidate":false,"about_ca_system_consensus":false,"about_ca_system_score_codex":0.0002450178,"about_ca_system_score_gemma":0.002382473,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_topic_score_codex":0.00004520648,"about_ca_topic_score_gemma":0.000188647,"domain_scores_codex":[0.9964284,0.000141426,0.001086314,0.0003226491,0.001582807,0.0004383831],"domain_scores_gemma":[0.998378,0.00005476366,0.0005526372,0.0003520059,0.0004520014,0.0002105879],"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":[0.00008244541,0.000105712,0.002459717,0.0001032466,0.0002714422,0.001304849,0.00008155569,0.001253518,0.002974275,0.000001118142,0.9690261,0.02233606],"study_design_scores_gemma":[0.001504567,0.0002204358,0.004255641,0.0002539163,0.0001334094,0.001286962,0.00004582126,0.0001473444,0.00186757,0.00005626541,0.9898609,0.0003671621],"study_design_candidate":"not_applicable","study_design_consensus":"not_applicable","genre_codex":"commentary","genre_gemma":"commentary","genre_scores_codex":[0.2329424,0.02721879,0.005928582,0.7271432,0.005672802,0.0003767957,0.0004109279,0.00001021711,0.0002962902],"genre_scores_gemma":[0.05243043,0.0344955,0.007783231,0.8268867,0.07508961,0.00004909857,0.0006306155,0.0003236863,0.002311144],"genre_candidate":"commentary","genre_consensus":"commentary","teacher_disagreement_score":0.180512,"threshold_uncertainty_score":0.9999626,"prediction_status":"machine_predicted_unvalidated"},"labels":[],"label_agreement":null},{"id":"W2097083248","doi":"10.1136/jmg.2003.013805","title":"<i>BRCA1 </i>functions as a breast stem cell regulator","year":2004,"lang":"en","type":"review","venue":"Journal of Medical Genetics","topic":"Animal Genetics and Reproduction","field":"Biochemistry, Genetics and Molecular Biology","cited_by":185,"is_retracted":false,"has_abstract":true,"routes":{"ca_aff":true,"ca_fund":false,"ca_venue":false,"about_ca":false},"ca_institutions":"McGill University; McGill University Health Centre; Montreal General Hospital","funders":"","keywords":"Breast cancer; Stem cell; Regulator; CD44; Biology; Cancer stem cell; Cancer research; Phenotype; CD24; Cancer; Internal medicine; Cell; Gene; Genetics; Medicine","retraction":null,"screen_n_in":null,"score":{"opus":0.0180308134354694,"gpt":0.2983034999770426,"spread":0.2802726865415732,"validation_status":"score_only:v0-immature-baseline"},"prediction":{"model_version":"codex-gemma-dda1882f352a","candidate_categories":["metaepi_narrow"],"consensus_categories":[],"category_scores_codex":[0.0007545713,0.0004155615,0.0009900042,0.0001447847,0.00008872321,0.00004664264,0.0007424242,0.001117539,0.0001037915],"category_scores_gemma":[0.00006083861,0.0003063257,0.0008821969,0.0002154777,0.0001777133,0.000002558357,0.0002395675,0.0007623374,0.00006793602],"about_ca_system_candidate":false,"about_ca_system_consensus":false,"about_ca_system_score_codex":0.00007319453,"about_ca_system_score_gemma":0.002843358,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_topic_score_codex":0.000002754336,"about_ca_topic_score_gemma":0.000002061723,"domain_scores_codex":[0.9966708,0.0001576119,0.001207727,0.0004544019,0.001176416,0.000333007],"domain_scores_gemma":[0.9975262,0.00001831622,0.001006947,0.0005480632,0.0003326237,0.0005678425],"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":[0.0000384262,0.0003344569,0.000005703122,0.003588142,0.0004178984,0.0001023391,0.00001830404,0.00004932852,0.0004522939,0.00002060369,0.008871219,0.9861013],"study_design_scores_gemma":[0.0004491213,0.0008600948,0.000007047117,0.002931424,0.0007338503,0.007104443,0.00003608964,0.000001811731,0.0002634211,0.0000227453,0.987276,0.0003139404],"study_design_candidate":"not_applicable","study_design_consensus":null,"genre_codex":"review","genre_gemma":"review","genre_scores_codex":[0.0006360227,0.9961141,0.0009178807,0.000197491,0.001592089,0.0002254336,0.00002967987,0.000005707321,0.0002815406],"genre_scores_gemma":[0.0003943254,0.9921349,0.000354791,0.00008339845,0.004165574,0.000006353285,0.00004412547,0.00008618343,0.002730303],"genre_candidate":"review","genre_consensus":"review","teacher_disagreement_score":0.9857873,"threshold_uncertainty_score":0.9999389,"prediction_status":"machine_predicted_unvalidated"},"labels":[],"label_agreement":null},{"id":"W2126856749","doi":"10.1136/jmg.40.6.e82","title":"Recurrent mutations in the <i>NF1</i> gene are common among neurofibromatosis type 1 patients","year":2003,"lang":"en","type":"article","venue":"Journal of Medical Genetics","topic":"Neurofibromatosis and Schwannoma Cases","field":"Medicine","cited_by":180,"is_retracted":false,"has_abstract":true,"routes":{"ca_aff":false,"ca_fund":false,"ca_venue":false,"about_ca":true},"ca_institutions":"","funders":"Institut Català de la Salut; Ministerio de Ciencia y Tecnología","keywords":"Medicine; Adverse effect; Rofecoxib; Guideline; Intensive care medicine; MEDLINE; Internal medicine; Pediatrics; Pathology","retraction":null,"screen_n_in":null,"score":{"opus":0.02719881660722146,"gpt":0.2918148162468842,"spread":0.2646159996396628,"validation_status":"score_only:v0-immature-baseline"},"prediction":{"model_version":"codex-gemma-dda1882f352a","candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0006634719,0.0001332502,0.0003478663,0.0001282336,0.00005973152,0.00003180166,0.0002477099,0.0001166609,0.00008707268],"category_scores_gemma":[0.00095715,0.00008339851,0.0001318805,0.0003805941,0.0001060516,0.00004280767,0.00002841585,0.0005518804,0.000008358207],"about_ca_system_candidate":false,"about_ca_system_consensus":false,"about_ca_system_score_codex":0.00002721334,"about_ca_system_score_gemma":0.0001766057,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_topic_score_codex":0.000003187336,"about_ca_topic_score_gemma":0.000007326627,"domain_scores_codex":[0.9971269,0.0003415181,0.000742232,0.0001198176,0.001460021,0.0002095288],"domain_scores_gemma":[0.9986623,0.0002414711,0.000364623,0.0002267843,0.0002087062,0.0002961176],"domain_codex":null,"domain_gemma":null,"domain_candidate":null,"domain_consensus":null,"study_design_codex":"observational","study_design_gemma":"observational","study_design_scores_codex":[0.0001115339,0.001314539,0.9780805,0.00007127882,0.00004379689,0.001277074,0.0003627397,0.00002227962,0.0003937623,0.00007102644,0.01489062,0.003360861],"study_design_scores_gemma":[0.002814935,0.002003303,0.9782503,0.0004517266,0.0001669726,0.00171906,0.0003719539,0.0001094538,0.003092692,0.0001768355,0.01070397,0.0001388132],"study_design_candidate":"observational","study_design_consensus":"observational","genre_codex":"empirical","genre_gemma":"empirical","genre_scores_codex":[0.995849,0.001205396,0.00001527728,0.001761735,0.0006157573,0.0001717444,0.000004278209,0.000005243316,0.0003716017],"genre_scores_gemma":[0.9974966,0.0007126632,0.0004019866,0.00121945,0.0001330072,0.000002414452,0.000005468531,0.00001783708,0.00001058511],"genre_candidate":"empirical","genre_consensus":"empirical","teacher_disagreement_score":0.004186647,"threshold_uncertainty_score":0.3400893,"prediction_status":"machine_predicted_unvalidated"},"labels":[],"label_agreement":null},{"id":"W2121184377","doi":"10.1136/jmg.2003.012518","title":"Intranuclear inclusions in neural cells with premutation alleles in fragile X associated tremor/ataxia syndrome","year":2004,"lang":"en","type":"letter","venue":"Journal of Medical Genetics","topic":"Genetics and Neurodevelopmental Disorders","field":"Biochemistry, Genetics and Molecular Biology","cited_by":176,"is_retracted":false,"has_abstract":true,"routes":{"ca_aff":true,"ca_fund":false,"ca_venue":false,"about_ca":false},"ca_institutions":"Université Laval","funders":"Eunice Kennedy Shriver National Institute of Child Health and Human Development","keywords":"FMR1; Ataxia; Fragile X syndrome; Intention tremor; Parkinsonism; Cerebellum; Cerebellar ataxia; Biology; Neuroscience; Pathology; Allele; Medicine; Genetics; Gene","retraction":null,"screen_n_in":null,"score":{"opus":0.007257658018037775,"gpt":0.2279789885496353,"spread":0.2207213305315976,"validation_status":"score_only:v0-immature-baseline"},"prediction":{"model_version":"codex-gemma-dda1882f352a","candidate_categories":["metaepi_narrow"],"consensus_categories":[],"category_scores_codex":[0.0003895047,0.0003124354,0.0004695989,0.0002564317,0.0000398195,0.00003172399,0.0006092613,0.001073823,0.00007111592],"category_scores_gemma":[0.0001504243,0.0002677534,0.0001191325,0.0002263629,0.0001318281,0.000004209524,0.0001968948,0.001669479,0.000003205927],"about_ca_system_candidate":false,"about_ca_system_consensus":false,"about_ca_system_score_codex":0.0000984862,"about_ca_system_score_gemma":0.0007094105,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_topic_score_codex":0.00002960163,"about_ca_topic_score_gemma":0.0003614578,"domain_scores_codex":[0.9970511,0.0001921911,0.0008286259,0.0003286842,0.001187864,0.0004114985],"domain_scores_gemma":[0.9990559,0.00003553648,0.0004391707,0.0001975942,0.0001100639,0.0001617916],"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":[0.001022055,0.00343713,0.01125555,0.0009779288,0.001212167,0.04010747,0.002632264,0.06040793,0.1066211,0.000002749693,0.7502443,0.02207932],"study_design_scores_gemma":[0.03719489,0.01642409,0.3001337,0.0058161,0.0006211773,0.006773028,0.0009523774,0.005858711,0.01893036,0.000866998,0.6013738,0.005054823],"study_design_candidate":"not_applicable","study_design_consensus":"not_applicable","genre_codex":"empirical","genre_gemma":"empirical","genre_scores_codex":[0.9398962,0.001603475,0.00007052222,0.05781889,0.0003186779,0.0002196147,0.00002277355,0.00000331139,0.0000465553],"genre_scores_gemma":[0.9262494,0.004158524,0.0007465184,0.06812546,0.0002492776,0.000005768626,0.0002473149,0.00009300996,0.0001247296],"genre_candidate":"empirical","genre_consensus":"empirical","teacher_disagreement_score":0.2888781,"threshold_uncertainty_score":0.9999775,"prediction_status":"machine_predicted_unvalidated"},"labels":[],"label_agreement":null},{"id":"W2164073493","doi":"10.1136/jmedgenet-2013-101795","title":"Delineating the genetic heterogeneity of ALS using targeted high-throughput sequencing","year":2013,"lang":"en","type":"article","venue":"Journal of Medical Genetics","topic":"Amyotrophic Lateral Sclerosis Research","field":"Medicine","cited_by":170,"is_retracted":false,"has_abstract":true,"routes":{"ca_aff":true,"ca_fund":false,"ca_venue":false,"about_ca":false},"ca_institutions":"Trinity College","funders":"Science Foundation Ireland","keywords":"TARDBP; Penetrance; C9orf72; Amyotrophic lateral sclerosis; Genetics; Biology; Mendelian inheritance; Population; Genetic heterogeneity; Disease; Gene; Allele; Trinucleotide repeat expansion; Medicine; SOD1; Pathology; Phenotype","retraction":null,"screen_n_in":null,"score":{"opus":0.0765775986499534,"gpt":0.3592215884003776,"spread":0.2826439897504242,"validation_status":"score_only:v0-immature-baseline"},"prediction":{"model_version":"codex-gemma-dda1882f352a","candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.001309773,0.0001617558,0.0005229826,0.0001003058,0.00008701281,0.00003129575,0.0004778241,0.0002232699,0.0008225609],"category_scores_gemma":[0.001237462,0.00009170145,0.0001965659,0.0002756152,0.0003007042,0.00006337083,0.0001931155,0.0007303656,0.00001175315],"about_ca_system_candidate":false,"about_ca_system_consensus":false,"about_ca_system_score_codex":0.0001785472,"about_ca_system_score_gemma":0.0007822936,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_topic_score_codex":0.0003303656,"about_ca_topic_score_gemma":0.000007112335,"domain_scores_codex":[0.9954012,0.0002569544,0.001233579,0.0001544097,0.002555143,0.0003987146],"domain_scores_gemma":[0.9975204,0.000228496,0.0005423074,0.0003299733,0.0008752095,0.0005035488],"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":[0.0001186149,0.0002625594,0.05046526,0.0002946335,0.0006637785,0.0003177903,0.0007344319,0.007308017,0.8724848,0.00002730544,0.00180085,0.06552198],"study_design_scores_gemma":[0.006604637,0.003305584,0.5032195,0.002264792,0.0007136799,0.004300857,0.0007916193,0.3113686,0.1651724,0.001030879,0.0007066539,0.0005208895],"study_design_candidate":"bench_or_experimental","study_design_consensus":null,"genre_codex":"empirical","genre_gemma":"empirical","genre_scores_codex":[0.9833822,0.002292124,0.0101132,0.003686422,0.0002338598,0.0002671114,0.000001821458,0.00000646017,0.00001678526],"genre_scores_gemma":[0.958913,0.001079199,0.03830833,0.0007423203,0.0009114877,0.000002328937,9.395761e-7,0.00002834916,0.00001399946],"genre_candidate":"empirical","genre_consensus":"empirical","teacher_disagreement_score":0.7073124,"threshold_uncertainty_score":0.9006464,"prediction_status":"machine_predicted_unvalidated"},"labels":[],"label_agreement":null},{"id":"W2123636830","doi":"10.1136/jmg.2008.058958","title":"High frequency of de novo mutations in Li–Fraumeni syndrome","year":2009,"lang":"en","type":"letter","venue":"Journal of Medical Genetics","topic":"Cancer-related Molecular Pathways","field":"Medicine","cited_by":169,"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":"Li–Fraumeni syndrome; Germline; Genetics; Germline mutation; Biology; Mutation; Cancer; Family history; Gene; Cancer research; Medicine; Internal medicine","retraction":null,"screen_n_in":null,"score":{"opus":0.01471162783883518,"gpt":0.2814100087304083,"spread":0.2666983808915732,"validation_status":"score_only:v0-immature-baseline"},"prediction":{"model_version":"codex-gemma-dda1882f352a","candidate_categories":["research_integrity"],"consensus_categories":["research_integrity"],"category_scores_codex":[0.0007485785,0.0002579403,0.0009872229,0.0006232215,0.00001660661,0.00001045963,0.0004450601,0.001695742,0.0005842957],"category_scores_gemma":[0.0008395623,0.0002281014,0.0003270732,0.0003842082,0.0001792593,0.00002207461,0.00004017838,0.00463582,0.00001050757],"about_ca_system_candidate":false,"about_ca_system_consensus":false,"about_ca_system_score_codex":0.0004175105,"about_ca_system_score_gemma":0.002789614,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_topic_score_codex":0.00004759254,"about_ca_topic_score_gemma":0.0000151994,"domain_scores_codex":[0.9953341,0.0001504176,0.001467854,0.000193156,0.002449133,0.0004053598],"domain_scores_gemma":[0.9980354,0.0001594543,0.0007845094,0.0003415547,0.0003149395,0.0003641169],"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":[0.0001352622,0.001036277,0.001877373,0.00139322,0.001245202,0.2483471,0.0008210525,0.0007943562,0.008232557,0.00005522218,0.7070681,0.02899428],"study_design_scores_gemma":[0.03504582,0.01375847,0.04495268,0.03216019,0.00664088,0.2624114,0.000227218,0.0008623833,0.01080136,0.0114861,0.5794061,0.002247348],"study_design_candidate":"not_applicable","study_design_consensus":"not_applicable","genre_codex":"commentary","genre_gemma":"commentary","genre_scores_codex":[0.3002047,0.01086605,0.003414373,0.683194,0.001462923,0.0003858485,0.00004096923,0.0000158336,0.0004152326],"genre_scores_gemma":[0.3138441,0.01153575,0.05340299,0.6099865,0.01010344,0.00001452132,0.0002148328,0.0002753767,0.0006224669],"genre_candidate":"commentary","genre_consensus":"commentary","teacher_disagreement_score":0.1276619,"threshold_uncertainty_score":0.9996003,"prediction_status":"machine_predicted_unvalidated"},"labels":[],"label_agreement":null},{"id":"W2098503979","doi":"10.1136/jmg.40.4.233","title":"Diagnostic criteria, clinical characteristics, and natural history of Cohen syndrome","year":2003,"lang":"en","type":"article","venue":"Journal of Medical Genetics","topic":"Blood disorders and treatments","field":"Biochemistry, Genetics and Molecular Biology","cited_by":167,"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; Faculty of Medicine and Health, University of Sydney; United Arab Emirates University; Samfundet Folkhälsan; Helsingin Yliopisto","keywords":"Natural history; Cohort; Pediatrics; Medicine; Genetic heterogeneity; Genetic testing; Genetic diagnosis; Homogeneous; Intellectual disability; Williams syndrome; Genetics; Pathology; Phenotype; Internal medicine; Psychiatry; Biology","retraction":null,"screen_n_in":null,"score":{"opus":0.01464307493127307,"gpt":0.2967257699598125,"spread":0.2820826950285394,"validation_status":"score_only:v0-immature-baseline"},"prediction":{"model_version":"codex-gemma-dda1882f352a","candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0005450303,0.0001047312,0.0003023244,0.00003162497,0.00001287329,0.000005497721,0.0001558457,0.00020238,0.00008938842],"category_scores_gemma":[0.001850791,0.00008418479,0.0001095697,0.00002164585,0.0002249213,0.00000226378,0.00004975503,0.0001849836,0.000001292982],"about_ca_system_candidate":false,"about_ca_system_consensus":false,"about_ca_system_score_codex":0.00001389465,"about_ca_system_score_gemma":0.0003273824,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_topic_score_codex":0.000002082967,"about_ca_topic_score_gemma":0.00000229099,"domain_scores_codex":[0.9986699,0.0001343097,0.0005851465,0.0001246683,0.0003539245,0.0001320736],"domain_scores_gemma":[0.9991097,0.0001011665,0.0002951233,0.0001379086,0.0001253562,0.0002307837],"domain_codex":null,"domain_gemma":null,"domain_candidate":null,"domain_consensus":null,"study_design_codex":"observational","study_design_gemma":"observational","study_design_scores_codex":[0.0003421894,0.002971874,0.8411856,0.0002699119,0.001583508,0.001418942,0.000264443,0.000001588214,0.009613689,0.0002258956,0.04389683,0.0982255],"study_design_scores_gemma":[0.01076282,0.006678855,0.6123943,0.0003869286,0.0007851022,0.004927282,0.0001629007,0.00009571826,0.00595259,0.0005081323,0.3567129,0.000632434],"study_design_candidate":"observational","study_design_consensus":"observational","genre_codex":"empirical","genre_gemma":"empirical","genre_scores_codex":[0.9670762,0.03112915,0.0001576878,0.0001590896,0.001311157,0.00005086017,0.000005543949,0.000001031795,0.0001092784],"genre_scores_gemma":[0.9884444,0.0100642,0.0008247392,0.0003085668,0.0001695681,8.304513e-7,0.000007116621,0.00001184747,0.0001687555],"genre_candidate":"empirical","genre_consensus":"empirical","teacher_disagreement_score":0.3128161,"threshold_uncertainty_score":0.3432956,"prediction_status":"machine_predicted_unvalidated"},"labels":[],"label_agreement":null},{"id":"W2277262967","doi":"10.1136/jmedgenet-2015-103322","title":"Clinical course of sly syndrome (mucopolysaccharidosis type VII)","year":2016,"lang":"en","type":"article","venue":"Journal of Medical Genetics","topic":"Lysosomal Storage Disorders Research","field":"Medicine","cited_by":165,"is_retracted":false,"has_abstract":true,"routes":{"ca_aff":true,"ca_fund":false,"ca_venue":false,"about_ca":false},"ca_institutions":"Université de Montréal; Centre Hospitalier Universitaire Sainte-Justine","funders":"Ultragenyx Pharmaceutical","keywords":"Mucopolysaccharidosis; Mucopolysaccharidosis I; Medicine; Bioinformatics; Genetics; Biology; Internal medicine; Disease; Enzyme replacement therapy","retraction":null,"screen_n_in":null,"score":{"opus":0.05455727318571904,"gpt":0.4135507156892446,"spread":0.3589934425035255,"validation_status":"score_only:v0-immature-baseline"},"prediction":{"model_version":"codex-gemma-dda1882f352a","candidate_categories":["insufficient_payload"],"consensus_categories":[],"category_scores_codex":[0.002130819,0.0001275707,0.0006748817,0.0001361487,0.00002268485,0.000006626858,0.000478684,0.0003376988,0.002513348],"category_scores_gemma":[0.003062334,0.00006998837,0.0002923222,0.0002752609,0.0004525942,0.00004010668,0.0001234245,0.0005570275,0.0000607677],"about_ca_system_candidate":false,"about_ca_system_consensus":false,"about_ca_system_score_codex":0.00005285903,"about_ca_system_score_gemma":0.001366112,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_topic_score_codex":0.000005370633,"about_ca_topic_score_gemma":0.000002759358,"domain_scores_codex":[0.9958085,0.0001618232,0.001170707,0.0001502736,0.002410097,0.0002986009],"domain_scores_gemma":[0.9971365,0.0004717949,0.0004020197,0.0003019047,0.0007945349,0.0008931975],"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":[0.001383582,0.002769465,0.4477708,0.0002487653,0.001168589,0.003939253,0.0001780026,0.000001385825,0.01204704,0.0001309354,0.03312709,0.4972351],"study_design_scores_gemma":[0.03195659,0.0282229,0.8033344,0.004875981,0.00139774,0.01802595,0.0007307102,0.0006074081,0.01590569,0.001771906,0.09243166,0.0007391078],"study_design_candidate":"observational","study_design_consensus":null,"genre_codex":"empirical","genre_gemma":"empirical","genre_scores_codex":[0.9809363,0.004762345,0.00137274,0.01181031,0.0007888331,0.0001160582,0.000004675254,0.000007366365,0.0002013287],"genre_scores_gemma":[0.9885458,0.00910501,0.001053598,0.0004482818,0.0004795815,6.528072e-7,5.560942e-7,0.00002490514,0.0003416292],"genre_candidate":"empirical","genre_consensus":"empirical","teacher_disagreement_score":0.496496,"threshold_uncertainty_score":0.9983985,"prediction_status":"machine_predicted_unvalidated"},"labels":[],"label_agreement":null},{"id":"W2129691431","doi":"10.1136/jmedgenet-2013-101658","title":"Phenotype and genotype in 101 males with X-linked creatine transporter deficiency","year":2013,"lang":"en","type":"article","venue":"Journal of Medical Genetics","topic":"Muscle metabolism and nutrition","field":"Biochemistry, Genetics and Molecular Biology","cited_by":165,"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":"Creatine; Genotype; Missense mutation; Genetics; Phenotype; Genotype-phenotype distinction; Intellectual disability; Medicine; Gene mutation; Epilepsy; Mutation; Internal medicine; Biology; Endocrinology; Gene; Psychiatry","retraction":null,"screen_n_in":null,"score":{"opus":0.008340379904614208,"gpt":0.2354437773250559,"spread":0.2271033974204417,"validation_status":"score_only:v0-immature-baseline"},"prediction":{"model_version":"codex-gemma-dda1882f352a","candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.000275698,0.00008786484,0.0001578227,0.00005171622,0.0000179355,0.00001382154,0.0001390285,0.0001437811,0.000153829],"category_scores_gemma":[0.00005235277,0.00006105618,0.00003134621,0.00006738233,0.00009255781,0.000004218403,0.00001875942,0.0001429054,0.000002088475],"about_ca_system_candidate":false,"about_ca_system_consensus":false,"about_ca_system_score_codex":0.000003228216,"about_ca_system_score_gemma":0.00008441327,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_topic_score_codex":0.00001264909,"about_ca_topic_score_gemma":0.00003309094,"domain_scores_codex":[0.9990517,0.00003896322,0.0003018891,0.0001090476,0.0003550264,0.0001432997],"domain_scores_gemma":[0.9995189,0.00001097676,0.0001001809,0.00009547042,0.0001092615,0.0001651601],"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":[0.001174066,0.001270633,0.2513113,0.0003626999,0.0001513672,0.0002212539,0.0007361769,0.0001230558,0.3997248,0.0002461453,0.003211115,0.3414673],"study_design_scores_gemma":[0.004719764,0.001686477,0.9642632,0.0001631509,0.00007816718,0.0002926904,0.0001867778,0.0003021978,0.009844022,0.0004250911,0.01775841,0.0002800476],"study_design_candidate":"observational","study_design_consensus":null,"genre_codex":"empirical","genre_gemma":"empirical","genre_scores_codex":[0.9887146,0.008287637,0.001987031,0.0007211775,0.00006943251,0.00007818623,0.000001695691,0.000001289508,0.0001389645],"genre_scores_gemma":[0.9884604,0.006660294,0.004257654,0.0002651558,0.000305317,0.000002323296,0.000006680879,0.00001037534,0.00003180973],"genre_candidate":"empirical","genre_consensus":"empirical","teacher_disagreement_score":0.7129519,"threshold_uncertainty_score":0.2489799,"prediction_status":"machine_predicted_unvalidated"},"labels":[],"label_agreement":null},{"id":"W2144252620","doi":"10.1136/jmg.40.3.175","title":"Clinical aspects, prenatal diagnosis, and pathogenesis of trisomy 16 mosaicism","year":2003,"lang":"en","type":"article","venue":"Journal of Medical Genetics","topic":"Prenatal Screening and Diagnostics","field":"Medicine","cited_by":164,"is_retracted":false,"has_abstract":true,"routes":{"ca_aff":true,"ca_fund":true,"ca_venue":false,"about_ca":false},"ca_institutions":"Children's & Women's Health Centre of British Columbia; University of British Columbia","funders":"Canadian Institutes of Health Research; Killam Trusts","keywords":"Trisomy; Amniocentesis; Aneuploidy; Prenatal diagnosis; Obstetrics; Chorionic villus sampling; Amniotic fluid; Pregnancy; Fetus; Biology; Intrauterine growth restriction; Medicine; Gynecology; Genetics; Chromosome","retraction":null,"screen_n_in":null,"score":{"opus":0.03419945740215336,"gpt":0.3395398522933712,"spread":0.3053403948912179,"validation_status":"score_only:v0-immature-baseline"},"prediction":{"model_version":"codex-gemma-dda1882f352a","candidate_categories":["metaresearch"],"consensus_categories":[],"category_scores_codex":[0.001869768,0.0001464026,0.0006476995,0.0001039848,0.00002939488,0.00001060047,0.000188701,0.0003406294,0.0002131261],"category_scores_gemma":[0.009901312,0.0001071602,0.000214324,0.0001538264,0.0002638851,0.00003106111,0.00007281046,0.0005653314,0.000003023699],"about_ca_system_candidate":false,"about_ca_system_consensus":false,"about_ca_system_score_codex":0.00002553949,"about_ca_system_score_gemma":0.0004911678,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_topic_score_codex":0.000007088854,"about_ca_topic_score_gemma":0.000003665772,"domain_scores_codex":[0.9969241,0.0002113434,0.001157275,0.0001599414,0.001323557,0.0002237653],"domain_scores_gemma":[0.9970418,0.001219437,0.0004286141,0.0002119147,0.0002371941,0.0008610457],"domain_codex":null,"domain_gemma":null,"domain_candidate":null,"domain_consensus":null,"study_design_codex":"observational","study_design_gemma":"observational","study_design_scores_codex":[0.0002567011,0.001266058,0.7096957,0.0002368979,0.0003157111,0.001101191,0.00009352805,0.000009223856,0.0001128021,0.0009353501,0.01110686,0.27487],"study_design_scores_gemma":[0.02294019,0.01068183,0.7727313,0.004286111,0.002289571,0.008127351,0.0005470047,0.0005745395,0.02909132,0.003173417,0.1448831,0.0006742674],"study_design_candidate":"observational","study_design_consensus":"observational","genre_codex":"empirical","genre_gemma":"empirical","genre_scores_codex":[0.9595214,0.03379672,0.003300692,0.001574196,0.0005574446,0.0001502617,0.00001570117,0.000009632577,0.001073982],"genre_scores_gemma":[0.9572409,0.03340304,0.008273777,0.0005247606,0.0004986795,0.000002200424,0.000003333088,0.00001926819,0.00003402486],"genre_candidate":"empirical","genre_consensus":"empirical","teacher_disagreement_score":0.2741957,"threshold_uncertainty_score":0.9984387,"prediction_status":"machine_predicted_unvalidated"},"labels":[],"label_agreement":null},{"id":"W2152652629","doi":"10.1136/jmedgenet-2013-101558","title":"Comprehensive molecular diagnosis of 179 Leber congenital amaurosis and juvenile retinitis pigmentosa patients by targeted next generation sequencing","year":2013,"lang":"en","type":"article","venue":"Journal of Medical Genetics","topic":"Retinal Development and Disorders","field":"Biochemistry, Genetics and Molecular Biology","cited_by":162,"is_retracted":false,"has_abstract":true,"routes":{"ca_aff":true,"ca_fund":true,"ca_venue":false,"about_ca":false},"ca_institutions":"McGill University; Montreal Children's Hospital","funders":"National Center for Research Resources; National Institute of General Medical Sciences; National Eye Institute; Canadian Institutes of Health Research; Research to Prevent Blindness; National Institutes of Health; Foundation Fighting Blindness; McGill University; Burroughs Wellcome Fund","keywords":"Retinitis pigmentosa; Sanger sequencing; Genetics; DNA sequencing; Biology; Mutation; Retinal Disorder; Medicine; Gene; Bioinformatics; Retinal; Ophthalmology","retraction":null,"screen_n_in":null,"score":{"opus":0.01923104549824916,"gpt":0.2390931131171032,"spread":0.2198620676188541,"validation_status":"score_only:v0-immature-baseline"},"prediction":{"model_version":"codex-gemma-dda1882f352a","candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.000149999,0.0001457116,0.000231956,0.00005049229,0.00004098805,0.00003675454,0.0001723908,0.0001982257,0.0001710496],"category_scores_gemma":[0.0002434619,0.0001288466,0.00008482367,0.00006982133,0.000137015,0.00001125226,0.00009958255,0.0001328874,0.000002400073],"about_ca_system_candidate":false,"about_ca_system_consensus":false,"about_ca_system_score_codex":0.00001618434,"about_ca_system_score_gemma":0.0001341072,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_topic_score_codex":0.0000258664,"about_ca_topic_score_gemma":0.000004292109,"domain_scores_codex":[0.9983659,0.00009553395,0.000559977,0.0001602287,0.0006378408,0.0001805677],"domain_scores_gemma":[0.9988748,0.00002759719,0.0003125264,0.0001038711,0.0004495648,0.0002316427],"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":[0.00003228952,0.0001316678,0.05225656,0.0000438369,0.0001662432,0.00001016878,0.000161387,0.00002997397,0.9043617,0.000004006397,0.02754997,0.01525225],"study_design_scores_gemma":[0.003305373,0.001706319,0.02231426,0.0001161718,0.000133158,0.00004350026,0.0004764912,0.001026409,0.9526579,0.00008117758,0.01769406,0.0004452238],"study_design_candidate":"bench_or_experimental","study_design_consensus":"bench_or_experimental","genre_codex":"empirical","genre_gemma":"empirical","genre_scores_codex":[0.9919928,0.006535022,0.0006558668,0.0003952668,0.0001825544,0.0001474504,0.00001183645,0.000001806745,0.0000773561],"genre_scores_gemma":[0.9909601,0.006567067,0.001693699,0.0005409974,0.00009650085,0.000009262959,0.00009046234,0.00001676965,0.00002510029],"genre_candidate":"empirical","genre_consensus":"empirical","teacher_disagreement_score":0.04829622,"threshold_uncertainty_score":0.5254212,"prediction_status":"machine_predicted_unvalidated"},"labels":[],"label_agreement":null},{"id":"W2120429387","doi":"10.1136/jmg.2005.037747","title":"Phenotype of triploid embryos: Table 1","year":2005,"lang":"en","type":"article","venue":"Journal of Medical Genetics","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":160,"is_retracted":false,"has_abstract":true,"routes":{"ca_aff":true,"ca_fund":false,"ca_venue":false,"about_ca":false},"ca_institutions":"Children's & Women's Health Centre of British Columbia; University of British Columbia","funders":"","keywords":"Biology; Phenotype; Genomic imprinting; Embryo; Genetics; Ploidy; Placenta; Fetus; Imprinting (psychology); Embryogenesis; Population; Embryonic stem cell; Andrology; Gene; Pregnancy; Gene expression; DNA methylation","retraction":null,"screen_n_in":null,"score":{"opus":0.01133265526969728,"gpt":0.2697541323457484,"spread":0.2584214770760511,"validation_status":"score_only:v0-immature-baseline"},"prediction":{"model_version":"codex-gemma-dda1882f352a","candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0006577858,0.0001031798,0.0002329049,0.00005099465,0.00002329826,0.000009910988,0.0004193644,0.0001985178,0.0002646848],"category_scores_gemma":[0.0004026997,0.0000846693,0.0001254346,0.00009166604,0.0000787306,0.000002287743,0.0001241398,0.0001675399,0.000006199359],"about_ca_system_candidate":false,"about_ca_system_consensus":false,"about_ca_system_score_codex":0.000008289486,"about_ca_system_score_gemma":0.000288254,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_topic_score_codex":0.000003163728,"about_ca_topic_score_gemma":0.000004568782,"domain_scores_codex":[0.9983731,0.00004442023,0.000607241,0.0001137799,0.0006601705,0.0002012967],"domain_scores_gemma":[0.9990088,0.00001737432,0.0003325065,0.0001996503,0.0002192595,0.0002223956],"domain_codex":null,"domain_gemma":null,"domain_candidate":null,"domain_consensus":null,"study_design_codex":"bench_or_experimental","study_design_gemma":"not_applicable","study_design_scores_codex":[0.0000664542,0.0005451363,0.007961931,0.00008515212,0.0002741014,0.00001262606,0.0001630178,0.001316345,0.7029017,0.00007305614,0.01743785,0.2691626],"study_design_scores_gemma":[0.003445428,0.00246354,0.014717,0.0001671207,0.0001259497,0.0007363895,0.0002942347,0.001345735,0.3998286,0.0001251478,0.5764066,0.0003443273],"study_design_candidate":"bench_or_experimental","study_design_consensus":null,"genre_codex":"empirical","genre_gemma":"empirical","genre_scores_codex":[0.9862307,0.007566424,0.00430398,0.0007358603,0.0003417973,0.00004582426,0.000002261217,0.00000174553,0.0007714624],"genre_scores_gemma":[0.9849305,0.00310893,0.01017439,0.00029961,0.001100632,5.68236e-7,0.000002389671,0.00001727503,0.0003656817],"genre_candidate":"empirical","genre_consensus":"empirical","teacher_disagreement_score":0.5589687,"threshold_uncertainty_score":0.3452714,"prediction_status":"machine_predicted_unvalidated"},"labels":[],"label_agreement":null}]}