{"meta":{"query_hash":"3b4090e3ab4b","filters":{"venue":"Clinical Dysmorphology"},"cohort_total":71,"direct_labels_cover":0,"predictions_cover":71,"exported":71,"export_cap":100000,"truncated":false,"label_status":"direct model label, unvalidated","prediction_status":"machine_predicted_unvalidated (Codex and Gemma teacher distillation)","score_status":"score_only:v0-immature-baseline","snapshot":{"source":"OpenAlex, pinned release, all 482 partitions","release":"2026-06-24","frame_built":"2026-07-12"},"permalink":"https://metacan.xera.ac/q/3b4090e3ab4b","api":"https://metacan.xera.ac/api/v1/cohort?venue=Clinical+Dysmorphology"},"results":[{"id":"W1968291594","doi":"10.1097/00019605-200104000-00007","title":"Two brothers with severe developmental delay, growth retardation and unusual appearance","year":2001,"lang":"en","type":"article","venue":"Clinical Dysmorphology","topic":"Epigenetics and DNA Methylation","field":"Biochemistry, Genetics and Molecular Biology","cited_by":1,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Alberta Children's Hospital; Royal University Hospital; University of Calgary; University of Saskatchewan","funders":"","keywords":"Medicine; Short stature; Growth retardation; Pediatrics; Differential diagnosis; Genetics; Pathology; Biology","score_opus":0.024559242667118023,"score_gpt":0.313902106961838,"score_spread":0.28934286429472,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1968291594","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.98985606,0.0006086124,0.0059595974,0.00024433047,0.00011458128,0.00014878433,0.000005021958,0.000012039721,0.0030509764],"genre_scores_gemma":[0.9930457,0.0008526779,0.004883004,0.0006032575,0.00017724883,0.00001095527,0.00008739154,0.00002092384,0.00031884664],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99884236,0.00013377825,0.00030447054,0.0004299013,0.000082697814,0.0002068057],"domain_scores_gemma":[0.9995344,0.000034419485,0.00009895722,0.00015703985,0.0000771485,0.00009803633],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0003580127,0.0001335417,0.00017276475,0.000027386157,0.00007039758,0.000015015937,0.000100608086,0.00019075914,0.00002806894],"category_scores_gemma":[0.00013650856,0.000116543786,0.000040167597,0.00007881534,0.00023969056,0.0000053264316,0.00007076302,0.00012764813,0.000020553744],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0009833823,0.00016786395,0.9028196,0.000013671975,0.00013269772,0.00009952752,0.000044832872,0.00006355768,0.06536121,0.00044169824,0.00050440145,0.029367588],"study_design_scores_gemma":[0.009947358,0.0040580058,0.8631154,0.000055898847,0.00011236866,0.0017534358,0.00017960218,0.00026482332,0.04036742,0.0024497826,0.07646961,0.0012262969],"about_ca_topic_score_codex":0.00002351512,"about_ca_topic_score_gemma":0.00008969998,"teacher_disagreement_score":0.07596521,"about_ca_system_score_codex":0.0000089037585,"about_ca_system_score_gemma":0.00006319926,"threshold_uncertainty_score":0.4752518},"labels":[],"label_agreement":null},{"id":"W1968301461","doi":"10.1097/mcd.0b013e328324440d","title":"A new syndrome of ankyloglossia and ulnar ray defects in a Newfoundland kindred","year":2009,"lang":"en","type":"article","venue":"Clinical Dysmorphology","topic":"Congenital heart defects research","field":"Biochemistry, Genetics and Molecular Biology","cited_by":1,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":true,"ca_institutions":"McMaster Children's Hospital; McMaster University","funders":"","keywords":"Medicine; Pediatrics; Family medicine; General surgery","score_opus":0.02531770742958537,"score_gpt":0.3534029505062576,"score_spread":0.3280852430766722,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1968301461","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9969492,0.0014607188,0.00016928973,0.00034656172,0.00010643502,0.00025284593,0.000007317606,0.000007900097,0.0006997478],"genre_scores_gemma":[0.9978854,0.00019591674,0.0008411732,0.0003913247,0.000088414476,0.000004321935,0.000026062118,0.000012383,0.0005550006],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99827766,0.00026295008,0.00049403834,0.00049785856,0.00010727709,0.0003602289],"domain_scores_gemma":[0.9990984,0.0001560875,0.000076033604,0.00040505687,0.00004823834,0.00021619185],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0005228038,0.00014423805,0.00041249304,0.000097530516,0.000023929904,0.00001064693,0.00019117977,0.00039406685,0.00006554255],"category_scores_gemma":[0.0006786504,0.00013823864,0.000115376744,0.00017777356,0.00024027567,0.0000040710165,0.00013804893,0.00026771676,0.000022342569],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0012233583,0.00048211738,0.72027004,0.000042810094,0.00007418959,0.0008426446,0.00004527694,0.000007641264,0.20665535,0.000314342,0.002073461,0.06796877],"study_design_scores_gemma":[0.0023447312,0.0034400136,0.987316,0.000018881901,0.000014619087,0.00047892387,0.0000055937035,0.00002247748,0.0008476295,0.0010140553,0.004331621,0.00016541609],"about_ca_topic_score_codex":0.00012106719,"about_ca_topic_score_gemma":0.00040165323,"teacher_disagreement_score":0.267046,"about_ca_system_score_codex":0.00001220165,"about_ca_system_score_gemma":0.00017212078,"threshold_uncertainty_score":0.5637208},"labels":[],"label_agreement":null},{"id":"W1969361900","doi":"10.1097/00019605-200204000-00018","title":"Bowen-Conradi syndrome","year":2002,"lang":"en","type":"letter","venue":"Clinical Dysmorphology","topic":"RNA regulation and disease","field":"Biochemistry, Genetics and Molecular Biology","cited_by":6,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":true,"ca_institutions":"University of Saskatchewan; Royal University Hospital","funders":"","keywords":"Medicine; Medical genetics; Family medicine; Pediatrics; Genetics","score_opus":0.04146344347090946,"score_gpt":0.31962342082187484,"score_spread":0.27815997735096537,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1969361900","genre_codex":"commentary","genre_gemma":"commentary","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"commentary","genre_consensus":"commentary","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.20372437,0.0038796347,0.0003491775,0.76709694,0.0068841944,0.00088324875,0.00041523163,0.00016168758,0.016605541],"genre_scores_gemma":[0.03749295,0.00044226766,0.00024534206,0.89049214,0.0059812022,0.000047456,0.0032587636,0.00011473184,0.06192514],"study_design_codex":"not_applicable","study_design_gemma":"not_applicable","domain_scores_codex":[0.9969376,0.00043853154,0.0008426688,0.0010480616,0.00019388058,0.0005392826],"domain_scores_gemma":[0.9980891,0.000109187225,0.00032408204,0.0011701188,0.00009392994,0.00021362978],"candidate_categories":["metaepi_narrow","research_integrity","insufficient_payload"],"consensus_categories":["insufficient_payload"],"category_scores_codex":[0.00027627367,0.00039385082,0.00063462445,0.000081187,0.000066784916,0.000028509989,0.0005638794,0.002992552,0.0022540956],"category_scores_gemma":[0.00049565855,0.00038103474,0.00060918863,0.00007773554,0.00055164256,0.0000023032303,0.00021396842,0.0011969587,0.001616372],"study_design_candidate":"not_applicable","study_design_consensus":"not_applicable","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.000036396486,0.00009251346,0.0045008254,0.000024558982,0.00012413439,0.002172244,0.0000011961139,0.000001639772,0.00012586833,0.000013285962,0.99206495,0.00084237265],"study_design_scores_gemma":[0.0008656932,0.0004860127,0.015969811,0.000011580872,0.00008971887,0.0007235763,0.0000010605925,0.000014192976,0.000015575282,0.00013880074,0.9812486,0.00043534357],"about_ca_topic_score_codex":0.0000038445996,"about_ca_topic_score_gemma":0.0000013537014,"teacher_disagreement_score":0.16623141,"about_ca_system_score_codex":0.000014431903,"about_ca_system_score_gemma":0.00010653244,"threshold_uncertainty_score":0.99986416},"labels":[],"label_agreement":null},{"id":"W1970050752","doi":"10.1097/mcd.0b013e3281e668fd","title":"Supernumerary nostrils together with oesophageal atresia and patent ductus arteriosus","year":2007,"lang":"en","type":"article","venue":"Clinical Dysmorphology","topic":"Congenital Ear and Nasal Anomalies","field":"Medicine","cited_by":14,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Pediatric Oncology Group","funders":"","keywords":"Medicine; Ductus arteriosus; Atresia; Supernumerary; Nostril; Anatomy; Cardiology; Nose","score_opus":0.053194000865640544,"score_gpt":0.3251343126431338,"score_spread":0.2719403117774933,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1970050752","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99348515,0.0011090152,0.00008216468,0.0012366115,0.0002985761,0.00024221976,0.00000845657,0.00006241106,0.0034754134],"genre_scores_gemma":[0.99415296,0.0001052673,0.0006987697,0.0024856143,0.0004038943,0.000003930395,0.000023639768,0.00002525934,0.0021006528],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9985546,0.00006607541,0.0004835275,0.00039849823,0.00012889515,0.0003684345],"domain_scores_gemma":[0.99890435,0.0003838776,0.00006278585,0.00026934297,0.00006691024,0.00031270675],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00045097785,0.00017338534,0.00046717565,0.000069980895,0.00005165129,0.000010183755,0.00006836414,0.00022837968,0.000548377],"category_scores_gemma":[0.00014294192,0.00011907795,0.00010668599,0.00010866676,0.00053060806,0.00004268207,0.000071345465,0.00034703934,0.00015367469],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.002895245,0.00027810948,0.93247426,0.000026147007,0.00013178452,0.006772951,0.00009181801,6.62456e-8,0.0015715867,0.00012471841,0.00095866655,0.054674625],"study_design_scores_gemma":[0.0029917555,0.0028034153,0.9854793,0.000018271412,0.00010822475,0.0022797298,0.000072261915,0.000004837722,0.00036210063,0.00009499452,0.0056424513,0.00014265251],"about_ca_topic_score_codex":0.00003470581,"about_ca_topic_score_gemma":0.000037650025,"teacher_disagreement_score":0.054531973,"about_ca_system_score_codex":0.000012219799,"about_ca_system_score_gemma":0.00007156604,"threshold_uncertainty_score":0.6004343},"labels":[],"label_agreement":null},{"id":"W1974995474","doi":"10.1097/00019605-200204000-00017","title":"Bowen-Conradi syndrome in non Hutterite infant","year":2002,"lang":"en","type":"letter","venue":"Clinical Dysmorphology","topic":"Synthesis and Characterization of Heterocyclic Compounds","field":"Chemistry","cited_by":5,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Alberta Children's Hospital; University of Calgary","funders":"","keywords":"Medicine; Pediatrics","score_opus":0.03784189224949927,"score_gpt":0.29494948662037246,"score_spread":0.25710759437087316,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1974995474","genre_codex":"empirical","genre_gemma":"commentary","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":null,"domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.72361106,0.0002038115,0.0000145300555,0.26067728,0.002180293,0.0001890078,0.00017440926,0.0001664326,0.012783189],"genre_scores_gemma":[0.3425116,0.0006342087,0.00013431863,0.6291682,0.005439924,0.00017566013,0.0016708098,0.00024636663,0.020018913],"study_design_codex":"not_applicable","study_design_gemma":"not_applicable","domain_scores_codex":[0.9950183,0.00021985054,0.0022140064,0.0013324351,0.00033356342,0.00088186434],"domain_scores_gemma":[0.9964887,0.0011986226,0.0007377032,0.0013788901,0.00005206376,0.00014404288],"candidate_categories":["metaepi_narrow","research_integrity","insufficient_payload"],"consensus_categories":["research_integrity","insufficient_payload"],"category_scores_codex":[0.00037951177,0.0006415188,0.0017407113,0.00024120114,0.000063629144,0.000074284646,0.0010283542,0.003522288,0.021715103],"category_scores_gemma":[0.00031768414,0.0006469125,0.0005840217,0.00014005406,0.00041085237,0.0000874572,0.0002931395,0.0041655977,0.0014903978],"study_design_candidate":"not_applicable","study_design_consensus":"not_applicable","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00005341738,0.00039263465,0.038451053,0.00031070656,0.00018539076,0.019414507,0.000043035998,5.83886e-7,0.0015934684,0.000003908866,0.93212575,0.0074255243],"study_design_scores_gemma":[0.0010535807,0.00010250801,0.042429138,0.0002614921,0.00006380713,0.0012154715,0.0000039634265,0.000081821934,0.00007140688,0.00007193908,0.9539309,0.0007139316],"about_ca_topic_score_codex":0.000035648336,"about_ca_topic_score_gemma":0.0000069265193,"teacher_disagreement_score":0.38109946,"about_ca_system_score_codex":0.00010011718,"about_ca_system_score_gemma":0.00004233146,"threshold_uncertainty_score":0.9995982},"labels":[],"label_agreement":null},{"id":"W1976703600","doi":"10.1097/mcd.0b013e3283377915","title":"Distal trisomy 10q syndrome: phenotypic features in a child with inverted duplicated 10q25.1–q26.3","year":2010,"lang":"en","type":"article","venue":"Clinical Dysmorphology","topic":"Genomic variations and chromosomal abnormalities","field":"Biochemistry, Genetics and Molecular Biology","cited_by":14,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":true,"ca_institutions":"Children's Hospital of Eastern Ontario; Dalhousie University; Izaak Walton Killam Health Centre; Holland Bloorview Kids Rehabilitation Hospital","funders":"","keywords":"Medicine; Nova scotia; Child health; Pediatrics; Medical genetics; Family medicine; Genealogy; Genetics; Archaeology; Biology; Geography","score_opus":0.007604253767183117,"score_gpt":0.2577041567816528,"score_spread":0.2500999030144697,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1976703600","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9964694,0.00010828755,0.00014986476,0.0009004787,0.0003511299,0.0002787699,0.0000485902,0.000030046827,0.001663433],"genre_scores_gemma":[0.9970806,0.000040838717,0.00063069415,0.00070191605,0.000203339,0.00006729274,0.000411401,0.00003366874,0.00083021144],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9982404,0.00013661492,0.0005378605,0.0006039353,0.000088428096,0.00039274103],"domain_scores_gemma":[0.9989752,0.0000653695,0.0001521742,0.0005921739,0.00007040859,0.00014467677],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00030276194,0.00023022224,0.0003768091,0.000069037,0.000096464224,0.000023610104,0.00034522792,0.0005386309,0.00023197092],"category_scores_gemma":[0.00022372346,0.00018983221,0.00012297579,0.00017792101,0.0004288634,0.000006078941,0.0001629318,0.0006521405,0.00006159937],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0026433475,0.0027221297,0.81889695,0.00007635372,0.0005875235,0.0011377727,0.00025012775,0.00007417503,0.14973335,0.006741511,0.009459361,0.007677426],"study_design_scores_gemma":[0.004223743,0.0014115511,0.9561616,0.000016840513,0.00005990741,0.003094805,0.00011760883,0.00003163038,0.0059828865,0.00042779787,0.027942311,0.0005292867],"about_ca_topic_score_codex":0.00009484812,"about_ca_topic_score_gemma":0.00077205064,"teacher_disagreement_score":0.14375046,"about_ca_system_score_codex":0.000009252891,"about_ca_system_score_gemma":0.00011342495,"threshold_uncertainty_score":0.77411324},"labels":[],"label_agreement":null},{"id":"W1977133238","doi":"10.1097/mcd.0b013e3282f449c8","title":"Characterizing the oculoauriculofrontonasal syndrome","year":2008,"lang":"en","type":"article","venue":"Clinical Dysmorphology","topic":"Ophthalmology and Eye Disorders","field":"Medicine","cited_by":28,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"North York General Hospital","funders":"","keywords":"Medicine","score_opus":0.07975073221822124,"score_gpt":0.3672508194348474,"score_spread":0.2875000872166261,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1977133238","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9778753,0.00028910482,0.00001773996,0.0100991875,0.00092748663,0.0002136713,0.000003019575,0.000069341375,0.010505161],"genre_scores_gemma":[0.9888197,0.00023334277,0.00019072111,0.008160959,0.00017650744,0.000017621862,0.00002814301,0.000018228622,0.0023547728],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9985853,0.00015258172,0.0004864197,0.0003365154,0.000108818815,0.00033038438],"domain_scores_gemma":[0.9988524,0.000414724,0.00010233266,0.00044304915,0.000050332736,0.00013717863],"candidate_categories":["insufficient_payload"],"consensus_categories":["insufficient_payload"],"category_scores_codex":[0.00044845106,0.00014056069,0.00044879527,0.000036708898,0.00020250924,0.0000026515386,0.00017287626,0.00032511447,0.0016388868],"category_scores_gemma":[0.00046112665,0.000089205365,0.000247428,0.00009525298,0.0010126433,0.0000401488,0.00007559018,0.00061935093,0.0014663888],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00041898456,0.00042664373,0.975296,0.000013976922,0.00019425037,0.01342997,0.00013091274,4.77143e-7,0.0006101844,0.00088584906,0.006976823,0.0016158805],"study_design_scores_gemma":[0.0010289955,0.0007690038,0.9441654,0.000008412445,0.00005871731,0.035140164,0.00004108974,0.000010942457,0.000026520695,0.00020300808,0.018448269,0.00009949063],"about_ca_topic_score_codex":0.000015233722,"about_ca_topic_score_gemma":0.0000011277758,"teacher_disagreement_score":0.031130664,"about_ca_system_score_codex":0.000016154292,"about_ca_system_score_gemma":0.000083794774,"threshold_uncertainty_score":0.9993111},"labels":[],"label_agreement":null},{"id":"W1980642562","doi":"10.1097/00019605-200207000-00008","title":"A second family with blepharo-naso-facial syndrome","year":2002,"lang":"en","type":"article","venue":"Clinical Dysmorphology","topic":"melanin and skin pigmentation","field":"Biochemistry, Genetics and Molecular Biology","cited_by":13,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Children's Hospital of Eastern Ontario","funders":"","keywords":"Medicine; Blepharophimosis; PAX3; Abnormality; Dermatology; Anatomy; Ptosis; Genetics; Gene; Surgery","score_opus":0.0396668125803937,"score_gpt":0.30252180044960375,"score_spread":0.26285498786921,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1980642562","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.986968,0.00030662533,0.000497926,0.00017609334,0.0005404835,0.00016199218,0.000023687659,0.000020501528,0.011304704],"genre_scores_gemma":[0.9894299,0.00015207547,0.0007445712,0.0027686257,0.00028883436,0.000023682749,0.00012240755,0.000024158158,0.006445783],"study_design_codex":"not_applicable","study_design_gemma":"not_applicable","domain_scores_codex":[0.99856436,0.00016265671,0.00039240194,0.0004918005,0.00010307322,0.00028571128],"domain_scores_gemma":[0.99929047,0.00004958296,0.00011458875,0.0003618244,0.000049425194,0.00013411234],"candidate_categories":["insufficient_payload"],"consensus_categories":[],"category_scores_codex":[0.00025254278,0.0001588106,0.0002596145,0.000031746826,0.00006434468,0.000014702069,0.00019820483,0.0003157424,0.001743134],"category_scores_gemma":[0.00009375252,0.00013431857,0.00010311101,0.00007459095,0.00025389012,0.0000037281636,0.00007243279,0.00018448652,0.00043546112],"study_design_candidate":"not_applicable","study_design_consensus":"not_applicable","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0012157307,0.0018295937,0.18503761,0.000069701004,0.00074006204,0.0021082987,0.0001629094,0.000027843556,0.37146106,0.0009619384,0.40952584,0.026859427],"study_design_scores_gemma":[0.008884203,0.008803976,0.3207317,0.000027014583,0.00013226457,0.002607276,0.00009998535,0.00013554025,0.011651001,0.00035921932,0.6455457,0.0010220845],"about_ca_topic_score_codex":0.000002263372,"about_ca_topic_score_gemma":0.0000140540715,"teacher_disagreement_score":0.35981005,"about_ca_system_score_codex":0.0000068545673,"about_ca_system_score_gemma":0.000024207591,"threshold_uncertainty_score":0.9991694},"labels":[],"label_agreement":null},{"id":"W1988243099","doi":"10.1097/mcd.0b013e3281e668eb","title":"Cytogenetic and molecular characterization of a de-novo cryptic deletion of 7p21 associated with an apparently balanced translocation and complex craniosynostosis","year":2007,"lang":"en","type":"article","venue":"Clinical Dysmorphology","topic":"Craniofacial Disorders and Treatments","field":"Biochemistry, Genetics and Molecular Biology","cited_by":4,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Children's Hospital of Eastern Ontario; Alberta Children's Hospital","funders":"Ulsan National Institute of Science and Technology","keywords":"Breakpoint; Chromosomal translocation; Craniosynostosis; Genetics; Phenotype; Craniofacial; Gene; Biology; Derivative chromosome; Chromosome; Chromosome 7 (human); Karyotype; Medicine; Chromosome 15","score_opus":0.022275344671934465,"score_gpt":0.3114003990967968,"score_spread":0.2891250544248623,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1988243099","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.98171705,0.00009754345,0.017865954,0.000046777754,0.000026082183,0.00019194976,0.000028598246,0.000005183643,0.000020884223],"genre_scores_gemma":[0.99843067,0.0002602957,0.0005924651,0.0001499946,0.000012006058,0.000005587258,0.0005312633,0.000013492396,0.000004233876],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9990572,0.00010983892,0.00036356447,0.00025863145,0.00006394178,0.00014687706],"domain_scores_gemma":[0.9994677,0.000032044158,0.00018443157,0.00014034592,0.00010246371,0.000073072515],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00027048576,0.000106190244,0.00024793044,0.000035439494,0.00002864082,0.00000390622,0.000053048763,0.00019823521,0.000008376248],"category_scores_gemma":[0.0000883724,0.000100084624,0.000037899354,0.00007595505,0.0002559883,0.0000040561777,0.000017629696,0.00004678861,2.4098728e-7],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00039951454,0.00031027157,0.20330217,0.000013218676,0.000075836295,0.000004889997,0.000037166403,0.0000023283333,0.7895673,0.000043626882,9.819407e-7,0.0062427],"study_design_scores_gemma":[0.0022081474,0.0019608974,0.9527793,0.000018499062,0.00008320117,0.000016301923,0.000028241691,0.000101323276,0.042585377,0.00008367984,0.000030478572,0.00010458694],"about_ca_topic_score_codex":0.000016174954,"about_ca_topic_score_gemma":0.000053533317,"teacher_disagreement_score":0.7494771,"about_ca_system_score_codex":0.000005166739,"about_ca_system_score_gemma":0.000028728273,"threshold_uncertainty_score":0.40813327},"labels":[],"label_agreement":null},{"id":"W1991068173","doi":"10.1097/mcd.0b013e32832a9ed5","title":"Punctate calcifications in lysosomal storage disorders","year":2009,"lang":"en","type":"article","venue":"Clinical Dysmorphology","topic":"Lysosomal Storage Disorders Research","field":"Medicine","cited_by":1,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Hospital for Sick Children","funders":"","keywords":"Medicine; Lysosomal storage disorders; Gerontology; Pathology; Disease","score_opus":0.05898818279521137,"score_gpt":0.41102630507674315,"score_spread":0.35203812228153175,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1991068173","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.95019877,0.00036188262,0.00047127067,0.027952775,0.00030628464,0.0006408134,0.000008025271,0.000111892754,0.019948272],"genre_scores_gemma":[0.99300873,0.00032890102,0.0006556511,0.0032491428,0.00014768957,0.00003503596,0.00007041243,0.00002097367,0.0024834743],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9972296,0.00031877385,0.0008715987,0.0006533763,0.0002874724,0.000639203],"domain_scores_gemma":[0.9983559,0.00042449907,0.000103781254,0.00067191984,0.000108622975,0.00033527848],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0007678245,0.00020321965,0.000621142,0.00026565065,0.00007448136,0.000014280851,0.00028497752,0.00037056385,0.00075831125],"category_scores_gemma":[0.001991791,0.00018081634,0.0002446701,0.0006351144,0.00045591858,0.00008383202,0.00006722096,0.0009434392,0.0007451261],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0013865554,0.0053410344,0.7979475,0.00003478023,0.00008249926,0.0016086681,0.00023855039,0.000057097044,0.0028128615,0.00468568,0.01725451,0.16855022],"study_design_scores_gemma":[0.0034962574,0.0012632486,0.96356994,0.000018470073,0.000029857925,0.000075286494,0.00008041086,0.00049399026,0.000025034533,0.0029490078,0.027811829,0.00018666235],"about_ca_topic_score_codex":0.000060781884,"about_ca_topic_score_gemma":0.0001090076,"teacher_disagreement_score":0.16836357,"about_ca_system_score_codex":0.00010148632,"about_ca_system_score_gemma":0.00020041518,"threshold_uncertainty_score":0.95773375},"labels":[],"label_agreement":null},{"id":"W1992274882","doi":"10.1097/01.mcd.0000198932.09330.33","title":"Duodenal and biliary atresia associated with facial, thyroid and auditory apparatus abnormalities: a new mandibulofacial dysostosis syndrome?","year":2006,"lang":"en","type":"review","venue":"Clinical Dysmorphology","topic":"Congenital Ear and Nasal Anomalies","field":"Medicine","cited_by":7,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Hospital for Sick Children; Mount Sinai Hospital; University of Toronto","funders":"","keywords":"Medicine; Atresia; Duodenal atresia; Choanal atresia; Biliary atresia; Microtia; Anatomy; Internal medicine; Liver transplantation","score_opus":0.05406500597751369,"score_gpt":0.34586339312688796,"score_spread":0.2917983871493743,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1992274882","genre_codex":"review","genre_gemma":"review","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"review","genre_consensus":"review","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.049969856,0.94608366,0.000008849478,0.00017920078,0.0006669723,0.0010152389,0.00032184858,0.00013070107,0.0016236424],"genre_scores_gemma":[0.0025327303,0.9815988,0.00010572781,0.00035587043,0.00096732023,0.000057815167,0.00068891083,0.00010259382,0.013590248],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.99597937,0.00047869197,0.0014911956,0.0010702134,0.0003161241,0.00066438975],"domain_scores_gemma":[0.9968657,0.0014395206,0.0005732429,0.00045114785,0.00009185759,0.0005785363],"candidate_categories":["metaepi_narrow","research_integrity"],"consensus_categories":[],"category_scores_codex":[0.0005948214,0.00075760385,0.0040026633,0.00029089814,0.00016388852,0.0000539168,0.00019072238,0.0015397114,0.00026842311],"category_scores_gemma":[0.00057816994,0.0005433893,0.00056371576,0.00032250374,0.001343485,0.0000875824,0.0002572979,0.0013555542,0.00011947742],"study_design_candidate":"not_applicable","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0011180255,0.0009210613,0.025665784,0.007444115,0.0033216875,0.010650797,0.000092933726,1.5610912e-7,0.0000017047148,0.00013087734,0.07591536,0.8747375],"study_design_scores_gemma":[0.0028762252,0.0034410583,0.048795506,0.0029373355,0.004458637,0.0059230886,0.000018343859,0.0000018518316,1.4953184e-7,0.00008143863,0.9307363,0.0007300839],"about_ca_topic_score_codex":0.000171051,"about_ca_topic_score_gemma":0.0001831509,"teacher_disagreement_score":0.8740074,"about_ca_system_score_codex":0.00008317753,"about_ca_system_score_gemma":0.0008621446,"threshold_uncertainty_score":0.9997565},"labels":[],"label_agreement":null},{"id":"W1998667446","doi":"10.1097/mcd.0b013e3282742611","title":"Familial mental retardation due to a cryptic subtelomeric translocation -del 14qter and dup 9qter (the Anyon phenotype)","year":2007,"lang":"en","type":"article","venue":"Clinical Dysmorphology","topic":"Genomic variations and chromosomal abnormalities","field":"Biochemistry, Genetics and Molecular Biology","cited_by":0,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Alberta Children's Hospital; University of Calgary","funders":"","keywords":"Microcephaly; dup; Subtelomere; Phenotype; Medicine; Chromosomal translocation; Short stature; Genetics; Pediatrics; Biology; Chromosome; Gene duplication; Gene","score_opus":0.01817667567798592,"score_gpt":0.292997322890966,"score_spread":0.2748206472129801,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1998667446","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9858351,0.00017596156,0.011503597,0.001348256,0.0005277046,0.00025781963,0.000015230059,0.000010844107,0.00032551555],"genre_scores_gemma":[0.99521726,0.00009678258,0.0011523144,0.0024392668,0.0004614622,0.000017719938,0.0001666383,0.00001559753,0.0004329505],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.99868375,0.0001491264,0.00047610985,0.0003612071,0.00007859447,0.00025119595],"domain_scores_gemma":[0.9994088,0.0000643365,0.00008554275,0.00027864915,0.00006311359,0.00009957801],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00084953976,0.00013259523,0.0001836743,0.000036620637,0.00012065144,0.00001743751,0.00014521471,0.00020290418,0.00009671735],"category_scores_gemma":[0.00010150766,0.00010631055,0.00008100598,0.000081846374,0.00018563363,0.000005947652,0.000078626224,0.00012516083,0.00008101209],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0021272958,0.0007349397,0.101463,0.000053411466,0.00039199824,0.00006906382,0.0023622701,0.0000791452,0.7407757,0.0022966545,0.009381776,0.14026476],"study_design_scores_gemma":[0.0020180573,0.0015227958,0.92451036,0.000011620653,0.0000893009,0.00022265803,0.0005122382,0.00013156632,0.021365238,0.00061931607,0.04855634,0.00044052652],"about_ca_topic_score_codex":0.000039016573,"about_ca_topic_score_gemma":0.00007966774,"teacher_disagreement_score":0.82304734,"about_ca_system_score_codex":0.00001409417,"about_ca_system_score_gemma":0.000037372527,"threshold_uncertainty_score":0.43352187},"labels":[],"label_agreement":null},{"id":"W1999470213","doi":"10.1097/01.mcd.0000220616.55402.03","title":"A form of autosomal dominant spondyloepiphyseal dysplasia is caused by a glycine to alanine substitution in the COL2A1 gene","year":2006,"lang":"en","type":"article","venue":"Clinical Dysmorphology","topic":"Connective tissue disorders research","field":"Biochemistry, Genetics and Molecular Biology","cited_by":8,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"St. Michael's Hospital","funders":"","keywords":"Medicine; Short stature; Dysplasia; Osteochondrodysplasia; Kyphosis; Anatomy; Pathology; Internal medicine; Surgery; Radiography","score_opus":0.023359582535043014,"score_gpt":0.3486608970486382,"score_spread":0.3253013145135952,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1999470213","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9953067,0.00039233698,0.000940374,0.0021887335,0.00011326063,0.0005770918,0.00011974886,0.0000054726793,0.00035630484],"genre_scores_gemma":[0.9979054,0.00006063942,0.00015654525,0.0008193115,0.00014964714,0.00007890471,0.00031905688,0.000017066943,0.0004934375],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9979762,0.00029669845,0.0006182963,0.00051085115,0.00018654243,0.00041145456],"domain_scores_gemma":[0.99901223,0.0001806835,0.000118287026,0.0004902571,0.00012502208,0.000073507064],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00086263893,0.00016718362,0.00035862633,0.00007862933,0.000048990572,0.000008587905,0.00040481938,0.00028603704,0.00009871369],"category_scores_gemma":[0.00054185954,0.00013162794,0.00012726242,0.0002911223,0.00034672965,0.0000037378416,0.00015856052,0.00022521256,0.000038127615],"study_design_candidate":"bench_or_experimental","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0012209099,0.0008061082,0.063555256,0.000015772526,0.000040059727,0.0000982639,0.00008398239,0.000011710333,0.90992224,0.00054046663,0.022584101,0.0011211209],"study_design_scores_gemma":[0.0065617296,0.004175527,0.63545805,0.000018337934,0.00004365923,0.00011656241,0.000096028496,0.00015324555,0.27636155,0.00069935696,0.07592887,0.0003870751],"about_ca_topic_score_codex":0.00038213347,"about_ca_topic_score_gemma":0.00082889345,"teacher_disagreement_score":0.6335607,"about_ca_system_score_codex":0.000022755694,"about_ca_system_score_gemma":0.0001132046,"threshold_uncertainty_score":0.53676313},"labels":[],"label_agreement":null},{"id":"W1999802043","doi":"10.1097/00019605-200104000-00003","title":"A new syndrome with craniofacial and skeletal dysmorphisms and developmental delay","year":2001,"lang":"en","type":"article","venue":"Clinical Dysmorphology","topic":"Tumors and Oncological Cases","field":"Medicine","cited_by":15,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Dalhousie University; McGill University; Montreal Children's Hospital","funders":"","keywords":"Medicine; Hypertelorism; Anatomy; Brachycephaly; Craniofacial; Anterior fontanelle; Craniofacial abnormality; Genu Valgum; Ossification; Nose; Orthodontics; Skull","score_opus":0.04228857563350174,"score_gpt":0.3292753617253956,"score_spread":0.2869867860918939,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1999802043","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9946791,0.0002809823,0.00054662686,0.0022402916,0.0001676901,0.0002874193,0.000005715006,0.000067685345,0.001724494],"genre_scores_gemma":[0.98304635,0.0002537992,0.01151119,0.0033139263,0.00020786791,0.000010547196,0.00001656777,0.000021627462,0.0016180984],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9983801,0.00007728577,0.00048813625,0.0005383775,0.00014923024,0.0003668358],"domain_scores_gemma":[0.9987731,0.00039182475,0.000086649125,0.00014340141,0.00004050421,0.0005645508],"candidate_categories":["insufficient_payload"],"consensus_categories":[],"category_scores_codex":[0.0002802275,0.00021582267,0.0006803394,0.00006102493,0.00009561835,0.00001742911,0.00006959609,0.0002838175,0.0012115437],"category_scores_gemma":[0.00035085526,0.00014710332,0.00006937274,0.00014578045,0.0006454333,0.000060220384,0.00012169456,0.0004152262,0.00008922162],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0012233709,0.00028775504,0.89684206,0.00001702043,0.000050696046,0.04671101,0.000044657165,1.4040462e-7,0.00010349963,0.00044114515,0.0030481825,0.051230464],"study_design_scores_gemma":[0.0042869453,0.004374996,0.83169067,0.000026519343,0.00010927174,0.12484405,0.000053655687,0.0000073746464,0.000004500156,0.00032490524,0.034090217,0.00018690006],"about_ca_topic_score_codex":0.00004643153,"about_ca_topic_score_gemma":0.000034264467,"teacher_disagreement_score":0.07813304,"about_ca_system_score_codex":0.000028832465,"about_ca_system_score_gemma":0.00017925169,"threshold_uncertainty_score":0.9997015},"labels":[],"label_agreement":null},{"id":"W2003468015","doi":"10.1097/mcd.0b013e328331dda5","title":"Large distal 5p deletion with hemifacial microsomia and absence of cri-du-chat syndrome","year":2009,"lang":"en","type":"article","venue":"Clinical Dysmorphology","topic":"Genomic variations and chromosomal abnormalities","field":"Biochemistry, Genetics and Molecular Biology","cited_by":5,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":true,"ca_institutions":"Alberta Children's Hospital; University of Calgary","funders":"","keywords":"Medicine; Hemifacial microsomia; Medical genetics; Family medicine; General surgery; Genetics; Psychiatry","score_opus":0.008282024099783215,"score_gpt":0.2594226842401786,"score_spread":0.2511406601403954,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2003468015","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99720496,0.0001870576,0.0017053913,0.00036018886,0.00011378562,0.00009570637,0.00006925305,0.000007892085,0.0002557812],"genre_scores_gemma":[0.99805707,0.00015444112,0.0008105441,0.00052461063,0.000112235684,0.000004250646,0.00013069104,0.000008479432,0.00019767859],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99898404,0.000066820685,0.000363874,0.00031548142,0.00005685736,0.00021293481],"domain_scores_gemma":[0.9994765,0.00002753029,0.00013290929,0.00022112505,0.00006878573,0.00007313185],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00021364473,0.00012325429,0.00024389129,0.000020744064,0.000066250395,0.000009727395,0.00011604754,0.00021220699,0.00004882342],"category_scores_gemma":[0.00007518006,0.00010522963,0.00006918336,0.000041116396,0.00024475378,0.000004859716,0.00007119533,0.000104106875,0.0000074936083],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0014596399,0.0012789163,0.54517,0.0000724114,0.00021510401,0.00026388082,0.0003293562,0.000034626104,0.43562773,0.009743232,0.0025200392,0.003285064],"study_design_scores_gemma":[0.0036260947,0.0057686823,0.9426735,0.00003200864,0.00007445466,0.0019700066,0.00028045417,0.000037485243,0.022598745,0.0012039379,0.02122776,0.00050683855],"about_ca_topic_score_codex":0.000008563393,"about_ca_topic_score_gemma":0.000017619712,"teacher_disagreement_score":0.413029,"about_ca_system_score_codex":0.000005287459,"about_ca_system_score_gemma":0.000046251695,"threshold_uncertainty_score":0.42911398},"labels":[],"label_agreement":null},{"id":"W2011342223","doi":"10.1097/00019605-200510000-00009","title":"Re: 3C (Ritscher???Schinzel) syndrome: the importance of ruling out a terminal 6p deletion","year":2005,"lang":"en","type":"article","venue":"Clinical Dysmorphology","topic":"Genomic variations and chromosomal abnormalities","field":"Biochemistry, Genetics and Molecular Biology","cited_by":4,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":true,"ca_institutions":"Alberta Children's Hospital","funders":"","keywords":"Medicine; Medical genetics; Family medicine; Genetics; Biology","score_opus":0.029354740611024614,"score_gpt":0.3179015095638546,"score_spread":0.28854676895283,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2011342223","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9947893,0.0005817248,0.0007965783,0.002256146,0.0003318075,0.00014058092,0.000027343534,0.0000112983635,0.0010652097],"genre_scores_gemma":[0.994285,0.00017903697,0.0021198313,0.0016101782,0.0005060159,0.000021385595,0.000086532615,0.000017132897,0.0011748977],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.998372,0.00019319914,0.0007418455,0.0003475011,0.00009180961,0.00025362056],"domain_scores_gemma":[0.9989656,0.000094418574,0.00028419663,0.0005019987,0.00008713444,0.00006661901],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0007318491,0.00014402969,0.0002669978,0.00002233513,0.000098492616,0.0000108629665,0.0003277688,0.0002902894,0.00020404036],"category_scores_gemma":[0.00030103934,0.00011088917,0.00019376731,0.000052571788,0.00029849447,0.000005611958,0.00016068539,0.0002292742,0.000059374433],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0009342966,0.0016226262,0.84819406,0.00013112894,0.00074453535,0.00030325327,0.00073585456,0.00065536395,0.09313936,0.005375041,0.024143085,0.024021411],"study_design_scores_gemma":[0.0051407088,0.004046043,0.5275077,0.00007919137,0.0003937929,0.0027175038,0.0012818043,0.0007031311,0.033616945,0.0023573618,0.4208522,0.0013035465],"about_ca_topic_score_codex":0.000008921674,"about_ca_topic_score_gemma":0.00012863656,"teacher_disagreement_score":0.39670914,"about_ca_system_score_codex":0.000010499179,"about_ca_system_score_gemma":0.00009080266,"threshold_uncertainty_score":0.4521929},"labels":[],"label_agreement":null},{"id":"W2016998274","doi":"10.1097/00019605-200207000-00002","title":"Tibial agenesis with radial ray and cardiovascular defects","year":2002,"lang":"en","type":"review","venue":"Clinical Dysmorphology","topic":"Congenital heart defects research","field":"Biochemistry, Genetics and Molecular Biology","cited_by":9,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Manitoba; Children's Hospital of Winnipeg","funders":"Canadian Institutes of Health Research; Medical Research Council Canada","keywords":"Medicine; Uterus didelphys; Imperforate anus; Agenesis; Renal agenesis; Anatomy; Uterus; Internal medicine","score_opus":0.08923720511551657,"score_gpt":0.3806576180396564,"score_spread":0.29142041292413984,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2016998274","genre_codex":"review","genre_gemma":"review","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"review","genre_consensus":"review","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.005387862,0.9922183,0.00010633293,0.00001156313,0.0004341216,0.00094578456,0.000061108854,0.000025102685,0.0008098186],"genre_scores_gemma":[0.0012685765,0.9952367,0.00024065294,0.00010095759,0.0013628361,0.00011976874,0.00024103443,0.00013114246,0.0012983183],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.99536127,0.001383653,0.000806082,0.0014992149,0.00027934124,0.0006704175],"domain_scores_gemma":[0.9975704,0.00038116114,0.00020734256,0.0013423609,0.0001039114,0.0003948287],"candidate_categories":["metaepi_narrow","research_integrity"],"consensus_categories":[],"category_scores_codex":[0.0009974781,0.0005622024,0.0024586616,0.00013644865,0.00010991039,0.000040987816,0.00043378858,0.0014945808,0.00016224236],"category_scores_gemma":[0.00087512215,0.0004363814,0.0014528666,0.00023195399,0.00083359476,0.0000031283378,0.0005383151,0.00077212416,0.00030253603],"study_design_candidate":"not_applicable","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.000069121095,0.00009613534,0.00017835035,0.0014059278,0.0013311699,0.00054643065,0.0000021505157,7.5880735e-7,0.000011497497,0.000004426356,0.0029758723,0.99337816],"study_design_scores_gemma":[0.0008712057,0.0013772872,0.00013548597,0.00032600056,0.0012301843,0.0010617995,0.0000014412702,0.000001845809,0.0000059950994,0.0000030651922,0.99448204,0.00050364755],"about_ca_topic_score_codex":0.000013386441,"about_ca_topic_score_gemma":0.000025681973,"teacher_disagreement_score":0.9928745,"about_ca_system_score_codex":0.000020768755,"about_ca_system_score_gemma":0.00031430085,"threshold_uncertainty_score":0.9998088},"labels":[],"label_agreement":null},{"id":"W2018448369","doi":"10.1097/00019605-200107000-00008","title":"De novo interstitial long arm deletion of chromosome 3 with facial dysmorphism, Dandy-Walker variant malformation and hydrocephalus","year":2001,"lang":"en","type":"article","venue":"Clinical Dysmorphology","topic":"Fetal and Pediatric Neurological Disorders","field":"Medicine","cited_by":20,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Manitoba; Health Sciences Centre","funders":"Johns Hopkins University","keywords":"Medicine; Facial dysmorphism; Hydrocephalus; Craniofacial; Anatomy; Craniofacial abnormality; Congenital hydrocephalus; Genetics; Surgery; Biology","score_opus":0.027270336730830062,"score_gpt":0.302995022314998,"score_spread":0.2757246855841679,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2018448369","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99148643,0.0001870751,0.004160695,0.0016983891,0.0002585689,0.0003042156,0.000013808723,0.000046896086,0.001843938],"genre_scores_gemma":[0.9959467,0.00065255136,0.00038592817,0.0024902648,0.00029550455,0.00001183332,0.000066847795,0.000015746176,0.00013461309],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99832743,0.00013224434,0.0006893665,0.00035658106,0.00016803347,0.0003263572],"domain_scores_gemma":[0.9990569,0.00025715135,0.00021313512,0.00018855833,0.00007779807,0.00020648712],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00038874405,0.00017852981,0.0005345353,0.00009873537,0.000057094832,0.000008785409,0.00009339838,0.00031459535,0.0006894265],"category_scores_gemma":[0.0003271771,0.00013040777,0.00013412006,0.00018923011,0.00056947576,0.00008738322,0.00007207229,0.000428718,0.000047225512],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.022568656,0.00426749,0.8450645,0.00064083765,0.00037023178,0.011444301,0.0006305088,0.000108789536,0.0040056375,0.0013960708,0.0016690232,0.10783391],"study_design_scores_gemma":[0.011023399,0.014252571,0.95099497,0.00009265304,0.0005721374,0.013694697,0.00005588962,0.0017118223,0.00012717517,0.0013797332,0.0057065934,0.00038835983],"about_ca_topic_score_codex":0.00003011842,"about_ca_topic_score_gemma":0.000016664077,"teacher_disagreement_score":0.107445545,"about_ca_system_score_codex":0.00002106283,"about_ca_system_score_gemma":0.00007391135,"threshold_uncertainty_score":0.7548737},"labels":[],"label_agreement":null},{"id":"W2019227423","doi":"10.1097/mcd.0b013e32823b007f","title":"Sudden death in a patient with mosaic ring X Turner syndrome and a neuronal migration disorder","year":2008,"lang":"en","type":"article","venue":"Clinical Dysmorphology","topic":"Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities","field":"Biochemistry, Genetics and Molecular Biology","cited_by":1,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Surrey Memorial Hospital","funders":"","keywords":"Medicine; Mosaic; Turner syndrome; Pediatrics; Ancient history","score_opus":0.01895464739446686,"score_gpt":0.2697947207016716,"score_spread":0.25084007330720476,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2019227423","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99857354,0.00027534115,0.000079627476,0.00043969127,0.00009005398,0.00013136724,0.000008203425,0.00000993178,0.00039224562],"genre_scores_gemma":[0.99743414,0.0004879419,0.00035911708,0.0010603587,0.0000578417,0.000024869312,0.00006221131,0.000013768362,0.0004997699],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9987045,0.00012273969,0.00044015152,0.0004135822,0.000097171884,0.00022185381],"domain_scores_gemma":[0.9995051,0.00007071344,0.00009249542,0.00018254612,0.000043280626,0.00010584679],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00012305625,0.0001437916,0.00023912928,0.00003452475,0.00006471555,0.000008528717,0.00009664896,0.00019105614,0.000054865155],"category_scores_gemma":[0.000110940506,0.00011356571,0.000060340437,0.00005710957,0.00031850828,0.0000057577176,0.000098095355,0.00017605943,0.00001137041],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00036213614,0.00053378753,0.9915481,0.000016194199,0.000042389736,0.0008872961,0.00012169471,0.00005403772,0.0011157129,0.00015852113,0.00039426377,0.004765831],"study_design_scores_gemma":[0.0016819992,0.0034088024,0.9823449,0.000016027827,0.000015729329,0.0024582949,0.000121589816,0.00011335011,0.0005097824,0.00015085435,0.008926185,0.00025247684],"about_ca_topic_score_codex":0.000038709724,"about_ca_topic_score_gemma":0.00017913923,"teacher_disagreement_score":0.009203226,"about_ca_system_score_codex":0.0000040414106,"about_ca_system_score_gemma":0.00004622287,"threshold_uncertainty_score":0.4631075},"labels":[],"label_agreement":null},{"id":"W2021049097","doi":"10.1097/00019605-200009010-00003","title":"New autosomal dominant syndrome reminiscent of Coffin-Siris syndrome and Brachymorphism-Onychodysplasia-Dysphalangism syndrome","year":2000,"lang":"en","type":"article","venue":"Clinical Dysmorphology","topic":"Chromatin Remodeling and Cancer","field":"Biochemistry, Genetics and Molecular Biology","cited_by":12,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Hospital for Sick Children","funders":"","keywords":"Clinodactyly; Medicine; Brachydactyly; Hypertelorism; Phalanx; Anatomy; Syndactyly; Hypoplasia; Craniofacial; Palpebral fissure; Short stature; Pediatrics","score_opus":0.015206328891406048,"score_gpt":0.2957403608430505,"score_spread":0.28053403195164445,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2021049097","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9938934,0.0026325376,0.0005258785,0.0006973841,0.00064574974,0.00031358967,0.00006525942,0.00003852872,0.0011877109],"genre_scores_gemma":[0.98781073,0.0013880309,0.0031488098,0.00060880074,0.00018292904,0.000017652152,0.00012919186,0.00006409103,0.0066497605],"study_design_codex":"design_other","study_design_gemma":"observational","domain_scores_codex":[0.99662536,0.00024626765,0.0012754697,0.001017546,0.00023973414,0.00059562264],"domain_scores_gemma":[0.99814826,0.00015962932,0.00031633108,0.000895644,0.00007053776,0.00040960393],"candidate_categories":["metaepi_narrow","insufficient_payload"],"consensus_categories":[],"category_scores_codex":[0.00064340874,0.00039372942,0.0009409359,0.00007786322,0.000094297706,0.000020196507,0.00046523497,0.00075611554,0.0012929912],"category_scores_gemma":[0.00019720697,0.00036834157,0.00032490114,0.00016232918,0.0005413215,0.000009802995,0.00021141309,0.00040041332,0.00015896707],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.004980696,0.0035331673,0.14750566,0.0009019279,0.0033240176,0.016849691,0.000476036,0.0009159915,0.24690372,0.0011693586,0.108839504,0.46460024],"study_design_scores_gemma":[0.014694271,0.01339793,0.70080787,0.0005641425,0.0007246919,0.104005605,0.000085533626,0.0006981159,0.009866417,0.0013891915,0.15138142,0.0023848056],"about_ca_topic_score_codex":0.00009533453,"about_ca_topic_score_gemma":0.000013970628,"teacher_disagreement_score":0.5533022,"about_ca_system_score_codex":0.000021342994,"about_ca_system_score_gemma":0.00024069278,"threshold_uncertainty_score":0.99987686},"labels":[],"label_agreement":null},{"id":"W2021165556","doi":"10.1097/00019605-200201000-00004","title":"Optic nerve coloboma, Dandy-Walker malformation, microglossia, tongue hamartomata, cleft palate and apneic spells: an existing oral-facial-digital syndrome or a new variant?","year":2002,"lang":"en","type":"article","venue":"Clinical Dysmorphology","topic":"Fetal and Pediatric Neurological Disorders","field":"Medicine","cited_by":13,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Saskatchewan; Royal University Hospital","funders":"","keywords":"Medicine; Polydactyly; Tongue; Coloboma; Anatomy; Pathology","score_opus":0.09707191619718204,"score_gpt":0.3391863241872559,"score_spread":0.2421144079900739,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2021165556","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99051404,0.00026983325,0.00012690692,0.0024823565,0.0005586468,0.00060812285,0.000074664604,0.00015379446,0.0052116243],"genre_scores_gemma":[0.9819626,0.00025257067,0.0019855811,0.0036437775,0.00036834308,0.000007100921,0.00014459567,0.00004687938,0.011588502],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99661607,0.000250614,0.0013618091,0.0008383482,0.00023402658,0.000699139],"domain_scores_gemma":[0.99749726,0.0007956066,0.0003217092,0.00050390046,0.00008849674,0.0007930016],"candidate_categories":["metaepi_narrow","insufficient_payload"],"consensus_categories":["insufficient_payload"],"category_scores_codex":[0.00051369163,0.0003927402,0.0010062396,0.00013024721,0.00012766433,0.000111219066,0.00025276822,0.00059045095,0.003946688],"category_scores_gemma":[0.0014412578,0.00029142277,0.00021559978,0.00038985617,0.0006152887,0.00037543898,0.00020080892,0.0007011222,0.0023077307],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.005605315,0.006894383,0.62236494,0.0007319229,0.0007361801,0.08816471,0.0011998175,0.00004575324,0.000580342,0.0010510624,0.11770299,0.1549226],"study_design_scores_gemma":[0.0141376965,0.014086559,0.8658437,0.000095581745,0.0007315616,0.04830171,0.00017615876,0.007850232,0.000009925011,0.0032895692,0.044248972,0.0012283267],"about_ca_topic_score_codex":0.000073589894,"about_ca_topic_score_gemma":0.000018315302,"teacher_disagreement_score":0.24347879,"about_ca_system_score_codex":0.000021587433,"about_ca_system_score_gemma":0.000081454564,"threshold_uncertainty_score":0.9999538},"labels":[],"label_agreement":null},{"id":"W2025702700","doi":"10.1097/mcd.0b013e32832a9e62","title":"Dysmorphology of Barth syndrome","year":2009,"lang":"en","type":"article","venue":"Clinical Dysmorphology","topic":"Mitochondrial Function and Pathology","field":"Biochemistry, Genetics and Molecular Biology","cited_by":25,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Institute of Infection and Immunity","funders":"Barth Syndrome Foundation","keywords":"Medicine; Xq28; Cardiolipins; Phenotype; Genetics; Gene; Cardiolipin; Membrane; Biology","score_opus":0.027545573396622735,"score_gpt":0.3291093843091941,"score_spread":0.3015638109125714,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2025702700","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.98627144,0.00037301998,0.0038152642,0.0010288036,0.0021137865,0.00021239078,0.000027029835,0.00003221023,0.0061260494],"genre_scores_gemma":[0.9887947,0.00021082087,0.0027007721,0.0053087845,0.00042101822,0.0000087255885,0.00017608574,0.000020015586,0.0023590953],"study_design_codex":"bench_or_experimental","study_design_gemma":"not_applicable","domain_scores_codex":[0.99752784,0.00042707386,0.0008853481,0.0006641491,0.000101665064,0.0003939359],"domain_scores_gemma":[0.9985783,0.00010366744,0.0002623219,0.0007547606,0.00012596605,0.00017497416],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00061920285,0.00021462944,0.0005754188,0.00008843652,0.00005064733,0.0000047397166,0.0003633868,0.00073007355,0.00074344146],"category_scores_gemma":[0.000787293,0.00020188105,0.00030333857,0.00014383749,0.00046674412,0.0000033862048,0.00010417531,0.00030010333,0.00024089732],"study_design_candidate":"bench_or_experimental","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0016818519,0.0012578774,0.053263795,0.000019318912,0.00017927117,0.000671083,0.000034108274,0.000042297772,0.83205384,0.007822373,0.084375605,0.018598584],"study_design_scores_gemma":[0.006885755,0.023377875,0.4549995,0.000024744928,0.00015994294,0.006699863,0.00005054475,0.000029970384,0.044705465,0.0047957352,0.45725054,0.0010200412],"about_ca_topic_score_codex":0.000004491298,"about_ca_topic_score_gemma":0.000007408705,"teacher_disagreement_score":0.7873484,"about_ca_system_score_codex":0.0000059742415,"about_ca_system_score_gemma":0.000090242414,"threshold_uncertainty_score":0.823247},"labels":[],"label_agreement":null},{"id":"W2030827199","doi":"10.1097/mcd.0000000000000030","title":"A report of a new case of an interstitial deletion at 3p25.3 and expansion of the clinical phenotype","year":2014,"lang":"en","type":"article","venue":"Clinical Dysmorphology","topic":"Genetic factors in colorectal cancer","field":"Medicine","cited_by":1,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"St. Michael's Hospital","funders":"National Institute for Health and Care Research","keywords":"Medicine; Phenotype; Clinical phenotype; Computational biology; Genetics; Gene","score_opus":0.07273065605059237,"score_gpt":0.41133367815655286,"score_spread":0.3386030221059605,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2030827199","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9971013,0.00007271219,0.00047078088,0.00040605746,0.0012942434,0.00027178897,0.0000062055024,0.000009260459,0.00036762893],"genre_scores_gemma":[0.99611497,0.000033685417,0.0030400923,0.00038389344,0.0002592523,0.0000028727688,0.000008352626,0.0000146674065,0.0001422111],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9974121,0.00043919423,0.0014921256,0.00036503916,0.00015308973,0.00013844756],"domain_scores_gemma":[0.99743867,0.00085869926,0.00066756294,0.0006808352,0.00018479863,0.00016945697],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0014788806,0.00011101082,0.0007187357,0.000039519437,0.00002113306,9.889551e-7,0.00011705537,0.00035218077,0.00024933575],"category_scores_gemma":[0.0047851824,0.00007645199,0.00020966328,0.0000963941,0.001099087,0.0000166997,0.00022936137,0.00029709845,0.0000029347607],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.008990793,0.0011802454,0.7757367,0.0002798087,0.00022532443,0.0014418577,0.00045808073,0.000014531076,0.03755092,0.00032114788,0.006353585,0.167447],"study_design_scores_gemma":[0.0072847405,0.017263977,0.9356457,0.00023354882,0.00063064834,0.015377971,0.00010104037,0.000700945,0.016725361,0.001227354,0.004601473,0.00020725888],"about_ca_topic_score_codex":0.00024346478,"about_ca_topic_score_gemma":0.00020395764,"teacher_disagreement_score":0.16723974,"about_ca_system_score_codex":0.000019997364,"about_ca_system_score_gemma":0.00025077458,"threshold_uncertainty_score":0.5728656},"labels":[],"label_agreement":null},{"id":"W2034763314","doi":"10.1097/mcd.0b013e32833593d1","title":"GAPO syndrome: a case associated with bilateral interstitial keratitis and hypothyroidism","year":2010,"lang":"en","type":"article","venue":"Clinical Dysmorphology","topic":"Connexins and lens biology","field":"Biochemistry, Genetics and Molecular Biology","cited_by":12,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Toronto; SickKids Foundation; Hospital for Sick Children","funders":"","keywords":"Medicine; Pediatrics; Dermatology","score_opus":0.014444957518337992,"score_gpt":0.2865103949918618,"score_spread":0.27206543747352385,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2034763314","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9977718,0.00010350359,0.00013370295,0.00063693715,0.0007326076,0.0001500018,0.000057112768,0.000023196219,0.00039111535],"genre_scores_gemma":[0.9971286,0.000056615416,0.00042294041,0.0014447889,0.00025644258,0.000017907523,0.00015955804,0.000024835153,0.00048833544],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.99845946,0.00019157388,0.0003827412,0.0005866487,0.00004582768,0.00033375924],"domain_scores_gemma":[0.9991236,0.00014889284,0.00011758952,0.0003597783,0.000076175646,0.00017401487],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00039044424,0.00019668501,0.00033617087,0.000040205432,0.000102121376,0.000023122911,0.00013422771,0.0006048162,0.00019711223],"category_scores_gemma":[0.0005899196,0.0001559694,0.000093279465,0.000057439433,0.00085116975,0.000003904772,0.000175113,0.00048546732,0.000018123668],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0017218508,0.0013015067,0.38126752,0.000025055271,0.0011148177,0.050979063,0.00015463274,0.0000035217822,0.5172079,0.0019827562,0.01857133,0.025670012],"study_design_scores_gemma":[0.013835793,0.023356292,0.60760564,0.000047452893,0.00033382987,0.24055493,0.00014967364,0.00026289065,0.006370621,0.00082839007,0.104692996,0.0019614797],"about_ca_topic_score_codex":0.000051281575,"about_ca_topic_score_gemma":0.0017595615,"teacher_disagreement_score":0.5108373,"about_ca_system_score_codex":0.000004410982,"about_ca_system_score_gemma":0.00007189253,"threshold_uncertainty_score":0.6360248},"labels":[],"label_agreement":null},{"id":"W2036220579","doi":"10.1097/01.mcd.0000228419.74413.1b","title":"Omphalocele in an infant with Cornelia de Lange syndrome","year":2006,"lang":"en","type":"article","venue":"Clinical Dysmorphology","topic":"Tumors and Oncological Cases","field":"Medicine","cited_by":3,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Royal University Hospital","funders":"","keywords":"Omphalocele; Cornelia de Lange Syndrome; Medicine; hirsutism; Pediatrics; Genetics; Pregnancy; Pathology; Biology","score_opus":0.049199843933880966,"score_gpt":0.372402714065979,"score_spread":0.32320287013209803,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2036220579","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99580264,0.00014219176,0.000051305156,0.0008257318,0.00010652953,0.00020855729,0.000008995788,0.000072521834,0.0027815073],"genre_scores_gemma":[0.9943194,0.0000135075115,0.001540317,0.003331581,0.00022013998,0.00002260895,0.00005826893,0.000017003173,0.00047718658],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9985477,0.00015561345,0.00047592592,0.00035831553,0.000095441144,0.00036703277],"domain_scores_gemma":[0.9990811,0.00032806693,0.000083631094,0.00027572882,0.000044747278,0.00018672507],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00045919733,0.0001273378,0.0005506774,0.00006080545,0.000023307335,0.0000071909017,0.000100130674,0.0002499949,0.00051119004],"category_scores_gemma":[0.00021081223,0.000085760184,0.0000714441,0.00016148586,0.00031839072,0.00003822114,0.000037588117,0.00039451185,0.000115397146],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00057081407,0.0009513351,0.9715869,0.0000111280315,0.000003526491,0.022105852,0.000006664156,0.000007397877,0.00014665024,0.00032952958,0.0036009022,0.00067930954],"study_design_scores_gemma":[0.0028232066,0.0053356467,0.9810431,0.000026286401,0.000038981154,0.004926227,0.00002089681,0.00007860837,0.000026000836,0.0004954984,0.00506755,0.000117992575],"about_ca_topic_score_codex":0.00039627403,"about_ca_topic_score_gemma":0.00048028163,"teacher_disagreement_score":0.017179625,"about_ca_system_score_codex":0.000050224968,"about_ca_system_score_gemma":0.000112186295,"threshold_uncertainty_score":0.55971724},"labels":[],"label_agreement":null},{"id":"W2037309563","doi":"10.1097/mcd.0b013e3283189762","title":"Spondylo-meta-epiphyseal dysplasia, short limb-abnormal calcification type","year":2008,"lang":"en","type":"article","venue":"Clinical Dysmorphology","topic":"Dermatological and Skeletal Disorders","field":"Biochemistry, Genetics and Molecular Biology","cited_by":11,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"St. Michael's Hospital","funders":"","keywords":"Medicine; Short stature; Brachydactyly; Anatomy; Dysplasia; Ossification; Craniofacial; Epiphysis; Pathology; Pediatrics","score_opus":0.11377240820657383,"score_gpt":0.35270638199498366,"score_spread":0.23893397378840983,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2037309563","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9903186,0.0008723558,0.0006555726,0.0006763956,0.00066314684,0.00019571437,0.000023065959,0.00004678729,0.0065483577],"genre_scores_gemma":[0.99285316,0.0009856905,0.0004532143,0.0025323546,0.00028554493,0.000033677043,0.0004962214,0.000025493178,0.002334652],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99775165,0.00030142762,0.0006816165,0.00067213894,0.00014746145,0.00044567976],"domain_scores_gemma":[0.99888307,0.000099748264,0.000102025784,0.0005598212,0.00013523211,0.00022008595],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00033557,0.00025457342,0.00054401916,0.00004365175,0.0001450103,0.00000918583,0.00037903062,0.00060217304,0.00040482142],"category_scores_gemma":[0.0005472018,0.00020224357,0.00046021788,0.00016810544,0.00074017205,0.000007017078,0.00018124843,0.00033074094,0.0005225626],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0032554439,0.003676024,0.61144143,0.000064995394,0.002884203,0.0015216282,0.000057974412,0.00010805295,0.09219377,0.0031481476,0.26272878,0.018919516],"study_design_scores_gemma":[0.0011556416,0.0027729692,0.5288452,0.0000026624057,0.00035402755,0.0013240395,0.000025362928,0.000086705906,0.005879864,0.00043700048,0.45841748,0.0006990725],"about_ca_topic_score_codex":0.000006942222,"about_ca_topic_score_gemma":0.00000967229,"teacher_disagreement_score":0.1956887,"about_ca_system_score_codex":0.0000063076927,"about_ca_system_score_gemma":0.00008287871,"threshold_uncertainty_score":0.82472533},"labels":[],"label_agreement":null},{"id":"W2039022811","doi":"10.1097/mcd.0b013e32835fff39","title":"Early childhood presentation of Czech dysplasia","year":2013,"lang":"en","type":"article","venue":"Clinical Dysmorphology","topic":"Connective tissue disorders research","field":"Biochemistry, Genetics and Molecular Biology","cited_by":11,"is_retracted":false,"has_abstract":true,"route_ca_aff":false,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"","funders":"Eunice Kennedy Shriver National Institute of Child Health and Human Development; Canadian Institutes of Health Research; National Human Genome Research Institute; Howard Hughes Medical Institute","keywords":"Medicine; Presentation (obstetrics); Czech; Pediatrics; Surgery","score_opus":0.026615612771874204,"score_gpt":0.35854484015177257,"score_spread":0.3319292273798984,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2039022811","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9958504,0.00025081992,0.0005344373,0.00041947968,0.00017404446,0.00040075448,0.000009063289,0.000009943118,0.0023510698],"genre_scores_gemma":[0.9981837,0.000105252155,0.0004042509,0.00018668902,0.00013897619,0.00005787207,0.00007630522,0.000019326817,0.0008276072],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9985341,0.0002672488,0.00042985054,0.00039379176,0.0001186666,0.0002563321],"domain_scores_gemma":[0.99901074,0.00013564473,0.00011690741,0.00042054415,0.00021801518,0.00009817148],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00029441048,0.000108374734,0.0002274885,0.000049951308,0.000031286112,0.000009053605,0.0002778421,0.00027203356,0.0006870239],"category_scores_gemma":[0.0011219694,0.000103964194,0.00012608299,0.00010445665,0.00033317757,0.000004907129,0.00019064985,0.00018539187,0.00032036332],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00019066976,0.000935452,0.49065325,0.000023079694,0.00024240761,0.000011737853,0.00013402083,0.000008316135,0.41587174,0.0004945084,0.019115442,0.072319366],"study_design_scores_gemma":[0.0010345217,0.0011267107,0.9741008,0.0000038642784,0.000010883142,0.000013160919,0.000057055615,0.000014647284,0.020094777,0.00086790824,0.0025602195,0.000115396324],"about_ca_topic_score_codex":0.000114696944,"about_ca_topic_score_gemma":0.00001530696,"teacher_disagreement_score":0.4834476,"about_ca_system_score_codex":0.0000043114687,"about_ca_system_score_gemma":0.00006901862,"threshold_uncertainty_score":0.752243},"labels":[],"label_agreement":null},{"id":"W2039715343","doi":"10.1097/mcd.0b013e328318c4fb","title":"Novel craniofacial and extracraniofacial findings in a case of Treacher Collins syndrome with a pathogenic mutation and a missense variant in the TCOF1 gene","year":2008,"lang":"en","type":"article","venue":"Clinical Dysmorphology","topic":"Craniofacial Disorders and Treatments","field":"Biochemistry, Genetics and Molecular Biology","cited_by":11,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":true,"ca_institutions":"McMaster University Medical Centre","funders":"","keywords":"Treacher Collins syndrome; Missense mutation; Medicine; Craniofacial; Genetics; Medical genetics; Mutation; Gene; Biology; Psychiatry","score_opus":0.0285183939321699,"score_gpt":0.29695784866630776,"score_spread":0.2684394547341379,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2039715343","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9988057,0.00020368876,0.00031783737,0.00013215732,0.000043287106,0.00037962678,0.00008203391,0.000003246558,0.000032431133],"genre_scores_gemma":[0.99867195,0.00028382696,0.00070484774,0.00020087567,0.000022345894,0.00003275007,0.00004526157,0.000014799016,0.000023368006],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99867827,0.00015771535,0.00044987613,0.00042609154,0.00007129722,0.00021674618],"domain_scores_gemma":[0.9995322,0.00009494481,0.000093772214,0.00018464774,0.00003248077,0.0000619355],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00035007184,0.00016846844,0.00034046808,0.00006137719,0.000072917384,0.000007124176,0.000074949065,0.0002797387,0.000008828419],"category_scores_gemma":[0.00015620438,0.00012584362,0.00006240374,0.0001558275,0.00045508033,0.000005693435,0.000042026208,0.00015997412,0.0000010135793],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0029213105,0.0042264652,0.68878,0.000051015,0.00024890137,0.21918906,0.003941748,0.000029283587,0.07450188,0.00018782067,0.000049669274,0.0058728443],"study_design_scores_gemma":[0.0074269916,0.0017502543,0.8517948,0.0000108419445,0.00006107381,0.13810158,0.00035171144,0.000065958666,0.000085151296,0.000079361904,0.00007830388,0.00019399471],"about_ca_topic_score_codex":0.00048396864,"about_ca_topic_score_gemma":0.0012344263,"teacher_disagreement_score":0.16301477,"about_ca_system_score_codex":0.0000073179717,"about_ca_system_score_gemma":0.00007329643,"threshold_uncertainty_score":0.51317537},"labels":[],"label_agreement":null},{"id":"W2045502094","doi":"10.1097/mcd.0b013e3283186907","title":"Sudden death in spondylo-meta-epiphyseal dysplasia, short limb-abnormal calcification type","year":2008,"lang":"en","type":"article","venue":"Clinical Dysmorphology","topic":"Dermatological and Skeletal Disorders","field":"Biochemistry, Genetics and Molecular Biology","cited_by":12,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of British Columbia","funders":"","keywords":"Medicine; Phalanx; Dysplasia; Anatomy; Pathology","score_opus":0.11821872547531381,"score_gpt":0.35789656411004567,"score_spread":0.23967783863473185,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2045502094","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.992979,0.0007936489,0.00023467421,0.00049592374,0.0004004708,0.00021104395,0.000016782345,0.000028073267,0.0048403796],"genre_scores_gemma":[0.9952979,0.0009827248,0.0003361111,0.0016027988,0.00016766092,0.000039341634,0.0003983152,0.000022546716,0.0011526081],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99764264,0.00034453245,0.00074691675,0.0006654677,0.00013415533,0.00046630946],"domain_scores_gemma":[0.99904823,0.00011430433,0.00009072486,0.0004808118,0.00009078219,0.00017514329],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00040985446,0.000244213,0.00057474483,0.00006763371,0.00008235013,0.000008081092,0.0003623946,0.0006107392,0.00025285778],"category_scores_gemma":[0.0005517481,0.00019985161,0.000339104,0.00019872311,0.0004512352,0.000007956671,0.00017137581,0.00036723824,0.0002616501],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0009784482,0.0011752509,0.96557105,0.00001804676,0.00039561887,0.0007535197,0.00002270214,0.00005053762,0.011223637,0.0009032237,0.016101118,0.0028068272],"study_design_scores_gemma":[0.0008856553,0.001252763,0.9292217,0.000002675035,0.00011175302,0.0005359083,0.000017365039,0.00007111712,0.0018205427,0.00034811065,0.06533978,0.00039264731],"about_ca_topic_score_codex":0.000023616114,"about_ca_topic_score_gemma":0.000047784946,"teacher_disagreement_score":0.04923866,"about_ca_system_score_codex":0.000009511668,"about_ca_system_score_gemma":0.00009029266,"threshold_uncertainty_score":0.8149712},"labels":[],"label_agreement":null},{"id":"W2047038997","doi":"10.1097/mcd.0b013e3282f16991","title":"A patient with de-novo partial deletion of Xp (p11.4–pter) and partial duplication of 22q (q11.2–qter)","year":2008,"lang":"en","type":"article","venue":"Clinical Dysmorphology","topic":"Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities","field":"Biochemistry, Genetics and Molecular Biology","cited_by":0,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Children's Hospital of Eastern Ontario","funders":"","keywords":"Medicine; Microcephaly; Gene duplication; Short stature; Genetics; Chromosomal translocation; Girl; Long arm; Chromosome; Pediatrics; Biology; Gene","score_opus":0.020348093205525993,"score_gpt":0.2854234657568125,"score_spread":0.2650753725512865,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2047038997","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9978082,0.00016288433,0.0010505266,0.00024274964,0.00011142218,0.00013988731,0.000017256343,0.000006984685,0.000460055],"genre_scores_gemma":[0.9978702,0.0005056726,0.000739276,0.00042922804,0.00025807627,0.000020723395,0.00005009307,0.000011130435,0.00011559643],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9985189,0.00014043521,0.0007028652,0.00032878068,0.00011364379,0.0001953636],"domain_scores_gemma":[0.999074,0.00008237008,0.00030831769,0.00026842984,0.00015377374,0.00011310507],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00021700756,0.00012834363,0.000312394,0.000021522208,0.00004970351,0.0000033166352,0.000110872796,0.00025266403,0.00009295244],"category_scores_gemma":[0.00017479974,0.00010583773,0.000100931815,0.000049022176,0.0008318416,0.0000048024167,0.000087469976,0.00010764879,0.000005542803],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00563549,0.003565418,0.7217385,0.00023438975,0.00044889428,0.00021823171,0.0009776518,0.00012493478,0.17296302,0.0025873568,0.003401675,0.08810438],"study_design_scores_gemma":[0.0064051775,0.020386657,0.5394737,0.00007884881,0.00019568077,0.0016871467,0.00048214,0.00034322595,0.39432874,0.00061790197,0.0352866,0.00071412796],"about_ca_topic_score_codex":0.000010243607,"about_ca_topic_score_gemma":0.00000616142,"teacher_disagreement_score":0.22136572,"about_ca_system_score_codex":0.000003803841,"about_ca_system_score_gemma":0.000080482416,"threshold_uncertainty_score":0.43159375},"labels":[],"label_agreement":null},{"id":"W2047267795","doi":"10.1097/mcd.0b013e328319edd9","title":"Macrocephaly, growth failure, translucent skin, renal cysts, coarctation of the aorta, and cholestasis: novel features of a new syndrome – the del17q12 syndrome","year":2009,"lang":"en","type":"article","venue":"Clinical Dysmorphology","topic":"Renal and related cancers","field":"Biochemistry, Genetics and Molecular Biology","cited_by":0,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":true,"ca_institutions":"McMaster University; McMaster Children's Hospital","funders":"","keywords":"Medicine; Macrocephaly; Pediatrics; Cholestasis; Coarctation of the aorta; Internal medicine; Aorta","score_opus":0.011860872308154672,"score_gpt":0.2790533787790092,"score_spread":0.2671925064708545,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2047267795","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9921278,0.0021295617,0.0003665412,0.0046827053,0.0002071267,0.00025102033,0.000041211806,0.0000059149584,0.00018814765],"genre_scores_gemma":[0.9970896,0.0009588691,0.0003103542,0.001161241,0.0000651782,0.0000051504053,0.00003550193,0.000012434832,0.00036165264],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9985167,0.00013513943,0.0005958609,0.00036399893,0.00015712388,0.00023118289],"domain_scores_gemma":[0.99908435,0.000064645355,0.0003012572,0.0003573962,0.00009300078,0.00009933075],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0003102766,0.00017459782,0.00035300505,0.000031020732,0.00006587206,0.0000076405695,0.0003853644,0.000417773,0.000012817898],"category_scores_gemma":[0.0001296816,0.00009934994,0.00025547307,0.00016327793,0.00058866455,0.0000047511908,0.00006619151,0.0003415897,0.000001693974],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0023289595,0.001729571,0.011468968,0.0002743238,0.0019992352,0.00026665026,0.00063469965,0.000312208,0.83970994,0.0035233353,0.0398396,0.09791254],"study_design_scores_gemma":[0.004445686,0.0028273195,0.91573757,0.00017924703,0.00042755928,0.0053850044,0.00010529011,0.000023339135,0.060539637,0.0015766509,0.008363295,0.00038937788],"about_ca_topic_score_codex":0.000070745074,"about_ca_topic_score_gemma":0.00004231232,"teacher_disagreement_score":0.9042686,"about_ca_system_score_codex":0.000007115622,"about_ca_system_score_gemma":0.0001313456,"threshold_uncertainty_score":0.4051373},"labels":[],"label_agreement":null},{"id":"W2049037612","doi":"10.1097/mcd.0b013e3282f16979","title":"Agnathia-otocephaly complex in a fetus with maternal use of topical 1% salicylate","year":2008,"lang":"en","type":"article","venue":"Clinical Dysmorphology","topic":"Hedgehog Signaling Pathway Studies","field":"Biochemistry, Genetics and Molecular Biology","cited_by":16,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":true,"ca_institutions":"Alberta Children's Hospital; McMaster University Medical Centre; McMaster Children's Hospital; University of Calgary","funders":"","keywords":"Medicine; Obstetrics and gynaecology; Medical genetics; University hospital; Family medicine; Gynecology; Pregnancy; Genetics","score_opus":0.1589998273519462,"score_gpt":0.35303092851258383,"score_spread":0.19403110116063763,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2049037612","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9986926,0.00009306041,0.00045011003,0.00016345788,0.00013299758,0.00019218422,0.000022609325,0.000013275353,0.00023974993],"genre_scores_gemma":[0.9958979,0.00014951217,0.002682406,0.0007154259,0.00014420584,0.000020961375,0.00003422046,0.000021920516,0.00033345906],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99819636,0.00024271118,0.0006709697,0.00045941287,0.000116395655,0.00031415137],"domain_scores_gemma":[0.99912304,0.00013590438,0.00016097502,0.00038824283,0.00009756256,0.00009429395],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00025316328,0.00017351459,0.00047232548,0.000054051878,0.000043475793,0.000004298404,0.00021653704,0.00028470333,0.000043859174],"category_scores_gemma":[0.00042622554,0.00014225968,0.00012054399,0.00010432292,0.00084906747,0.0000036203246,0.00018082737,0.00021792567,0.000018679717],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00060099893,0.00026175097,0.9157501,0.000013843084,0.00008293979,0.00051301875,0.00007586715,0.000054650147,0.080798,0.00007004557,0.0012985553,0.00048025153],"study_design_scores_gemma":[0.0017202337,0.001506804,0.97471756,0.000019567395,0.000016146312,0.00037274044,0.000014640949,0.000034514993,0.011436158,0.000037444348,0.009928325,0.0001958468],"about_ca_topic_score_codex":0.00010146318,"about_ca_topic_score_gemma":0.00015928874,"teacher_disagreement_score":0.06936184,"about_ca_system_score_codex":0.000009765733,"about_ca_system_score_gemma":0.000084917556,"threshold_uncertainty_score":0.5801181},"labels":[],"label_agreement":null},{"id":"W2051343849","doi":"10.1097/mcd.0b013e3282fdcc70","title":"Chondrodysplasia punctata: a clinical diagnostic and radiological review","year":2008,"lang":"en","type":"review","venue":"Clinical Dysmorphology","topic":"Peroxisome Proliferator-Activated Receptors","field":"Biochemistry, Genetics and Molecular Biology","cited_by":104,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"St. Thomas Hospital","funders":"","keywords":"Medicine; Chondrodysplasia punctata; Etiology; Peroxisomal disorder; Bioinformatics; Pathology; Internal medicine; Peroxisome; Biology","score_opus":0.09770023039027004,"score_gpt":0.4373722718057601,"score_spread":0.33967204141549007,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2051343849","genre_codex":"review","genre_gemma":"review","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"review","genre_consensus":"review","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.0014090391,0.9939467,0.00003961981,0.00018396346,0.002385679,0.0015785303,0.00013630558,0.000066294044,0.0002539145],"genre_scores_gemma":[0.000035417586,0.991601,0.0004690691,0.0031658409,0.0022780888,0.00037542483,0.0014965737,0.0001454818,0.00043311677],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.98913324,0.0036849033,0.0036321864,0.0024655,0.00022460465,0.000859538],"domain_scores_gemma":[0.9932784,0.003195661,0.0011668903,0.0014957244,0.00014417116,0.00071917387],"candidate_categories":["metaresearch","metaepi_narrow","research_integrity"],"consensus_categories":["research_integrity"],"category_scores_codex":[0.0017407716,0.0010762896,0.0055525918,0.000107377724,0.00015006801,0.000023621991,0.0009862423,0.0037806132,0.00021814267],"category_scores_gemma":[0.021029104,0.0007907098,0.0018886108,0.00030082787,0.0021516262,0.0000074679797,0.0009610425,0.0024122235,0.00053781975],"study_design_candidate":"not_applicable","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.000064379885,0.0005160207,0.002110882,0.005376449,0.0008365383,0.0005604173,0.0000016067678,5.354571e-8,0.000009018303,0.000019501083,0.20420972,0.7862954],"study_design_scores_gemma":[0.0007546216,0.0014416379,0.00022964909,0.0049431976,0.0007996339,0.0048940866,9.919966e-7,3.1177598e-7,0.0000037726172,0.000013042401,0.98611736,0.00080170616],"about_ca_topic_score_codex":0.0000019539618,"about_ca_topic_score_gemma":0.0000017427678,"teacher_disagreement_score":0.78549373,"about_ca_system_score_codex":0.000036052028,"about_ca_system_score_gemma":0.000724412,"threshold_uncertainty_score":0.99988925},"labels":[],"label_agreement":null},{"id":"W2058633552","doi":"10.1097/mcd.0b013e328325ee66","title":"Trisomy 9p and Prader–Willi syndromes in an infant resulting from a de-novo unbalanced t(9;15) translocation","year":2009,"lang":"en","type":"article","venue":"Clinical Dysmorphology","topic":"Genomic variations and chromosomal abnormalities","field":"Biochemistry, Genetics and Molecular Biology","cited_by":0,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Diagnostic Services Manitoba; University of Alberta; Children's Hospital of Eastern Ontario","funders":"","keywords":"Chromosomal translocation; Derivative chromosome; Hypertelorism; Fluorescence in situ hybridization; Medicine; Trisomy; Genetics; Chromosome 4; Chromosome 15; Biology; Chromosome; Anatomy; Gene","score_opus":0.030307991066889164,"score_gpt":0.3344652881644936,"score_spread":0.3041572970976045,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2058633552","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99711394,0.00063408405,0.0007684859,0.0010300876,0.00011295648,0.00014948002,0.00003791348,0.000015057902,0.00013796332],"genre_scores_gemma":[0.9953477,0.00041896725,0.002638087,0.0010428062,0.00020148848,0.0000145809645,0.0002634705,0.000010707807,0.00006220829],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9984194,0.0002554011,0.00056565297,0.0004407256,0.00005085589,0.00026795303],"domain_scores_gemma":[0.99936324,0.00008352164,0.00012140589,0.0002895958,0.00004051147,0.000101729594],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0004546795,0.0001368738,0.00027702263,0.000042502103,0.000056525518,0.000021789272,0.00015393777,0.00034978022,0.000028870189],"category_scores_gemma":[0.0002425475,0.00013348574,0.000058290196,0.000071108254,0.0001236174,0.000010305769,0.000032465286,0.00018656821,0.00000529449],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00034454258,0.0007092489,0.7717958,0.000014594428,0.00007890768,0.00006265848,0.0009121741,0.00015957604,0.18738131,0.0008336085,0.00033381622,0.037373744],"study_design_scores_gemma":[0.002654327,0.0011162915,0.9876413,0.000020751377,0.000022890517,0.00011039762,0.0002609795,0.00027475675,0.0035058353,0.0017990331,0.0023512086,0.00024228149],"about_ca_topic_score_codex":0.00008892696,"about_ca_topic_score_gemma":0.00018244128,"teacher_disagreement_score":0.21584544,"about_ca_system_score_codex":0.00001264858,"about_ca_system_score_gemma":0.000087995824,"threshold_uncertainty_score":0.54433906},"labels":[],"label_agreement":null},{"id":"W2059108712","doi":"10.1097/mcd.0b013e32832a9e0c","title":"Childhood-onset hemiatrophy caused by unilateral morphea","year":2009,"lang":"en","type":"article","venue":"Clinical Dysmorphology","topic":"Systemic Sclerosis and Related Diseases","field":"Medicine","cited_by":5,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":true,"ca_institutions":"University of British Columbia","funders":"","keywords":"Medicine; Morphea; Medical genetics; Family medicine; Pediatrics; Dermatology; Genetics","score_opus":0.02644322753228758,"score_gpt":0.3315153020136168,"score_spread":0.3050720744813292,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2059108712","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9880118,0.002379019,0.000028383478,0.006280168,0.0008800125,0.00035988228,0.00005098598,0.00018505918,0.0018246947],"genre_scores_gemma":[0.98010045,0.00072893966,0.00015387776,0.016760124,0.0005035679,0.0000097112315,0.0002515868,0.000027665159,0.0014641007],"study_design_codex":"not_applicable","study_design_gemma":"observational","domain_scores_codex":[0.997499,0.00021562539,0.0010037653,0.00059431215,0.0002099766,0.0004773347],"domain_scores_gemma":[0.99834216,0.00025269092,0.0001942478,0.00060708757,0.00008228485,0.0005215503],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00035155422,0.0002503754,0.0007934435,0.00007382611,0.00008199521,0.000015394719,0.00018301325,0.00061216374,0.0008040107],"category_scores_gemma":[0.00045303802,0.00019085947,0.00040825293,0.00020744684,0.00026072306,0.00004159013,0.000039240775,0.00059357315,0.00063884497],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00063259935,0.0034699603,0.26064068,0.000026077969,0.0003508392,0.0008500572,0.00009366358,0.000004172781,0.015143148,0.00018791558,0.70279247,0.015808398],"study_design_scores_gemma":[0.0057787434,0.001899018,0.9794451,0.00019197789,0.000333158,0.00053472794,0.000033595377,0.000034261986,0.0005163055,0.00033960657,0.010609202,0.0002843083],"about_ca_topic_score_codex":0.000012475756,"about_ca_topic_score_gemma":3.0043364e-7,"teacher_disagreement_score":0.7188044,"about_ca_system_score_codex":0.00004190813,"about_ca_system_score_gemma":0.00013018957,"threshold_uncertainty_score":0.88033533},"labels":[],"label_agreement":null},{"id":"W2060083017","doi":"10.1097/mcd.0b013e3280e1cc54","title":"Preaxial polydactyly in neurofibromatosis 1","year":2007,"lang":"en","type":"article","venue":"Clinical Dysmorphology","topic":"Neurofibromatosis and Schwannoma Cases","field":"Medicine","cited_by":6,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of British Columbia","funders":"","keywords":"Medicine; Neurofibromatosis; Polydactyly; Anatomy; Etiology; Axial skeleton; Neurofibromatosis type I; Pathology","score_opus":0.05530387641872618,"score_gpt":0.3859644300754109,"score_spread":0.33066055365668473,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2060083017","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.988749,0.00014889876,0.00009315012,0.0014647652,0.00088119536,0.00030048858,0.0000062673616,0.00011197613,0.008244261],"genre_scores_gemma":[0.9943274,0.000036871184,0.0010095608,0.003786923,0.00035876405,0.0000074282734,0.000018033812,0.000037287627,0.00041770196],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99726224,0.00018035821,0.0012040412,0.00057714555,0.00019775901,0.0005784807],"domain_scores_gemma":[0.99785304,0.001068973,0.00014907395,0.00052752934,0.00004871294,0.00035264157],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0010335553,0.00019949488,0.0006980643,0.0002272814,0.000040177787,0.0000117286745,0.00015548078,0.00034666297,0.0004208306],"category_scores_gemma":[0.0010638088,0.00017442502,0.0002703385,0.0003440026,0.0003083755,0.00006376656,0.000112816546,0.0005746761,0.00036943352],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0013293751,0.0008463889,0.9594772,0.000029296814,0.000024989802,0.0067212214,0.000026566448,2.241868e-7,0.018733779,0.0007194955,0.005152335,0.00693912],"study_design_scores_gemma":[0.0026670687,0.0015170111,0.9800551,0.0000380099,0.000038955313,0.002143745,0.00002674181,0.000020665919,0.0032246117,0.00017047509,0.009939746,0.00015787095],"about_ca_topic_score_codex":0.000030314277,"about_ca_topic_score_gemma":0.00001967228,"teacher_disagreement_score":0.02057789,"about_ca_system_score_codex":0.00002661596,"about_ca_system_score_gemma":0.00009023167,"threshold_uncertainty_score":0.7112846},"labels":[],"label_agreement":null},{"id":"W2061952005","doi":"10.1097/mcd.0b013e328328d4b9","title":"Diaphragmatic hernia and limb abnormalities syndrome (Froster syndrome)","year":2009,"lang":"en","type":"article","venue":"Clinical Dysmorphology","topic":"Congenital Diaphragmatic Hernia Studies","field":"Medicine","cited_by":0,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":true,"ca_institutions":"Ontario Power Generation; SickKids Foundation; Hospital for Sick Children; University of Toronto","funders":"","keywords":"Medicine; Diaphragmatic hernia; Congenital diaphragmatic hernia; Diaphragmatic breathing; Hernia; Surgery; Pathology; Pregnancy; Genetics","score_opus":0.03244566570958191,"score_gpt":0.3431936148140281,"score_spread":0.3107479491044462,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2061952005","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.98376685,0.0017264051,0.00003687847,0.007741459,0.00046365493,0.000547051,0.00002296825,0.00017457522,0.0055201347],"genre_scores_gemma":[0.98670244,0.00035894956,0.0007891886,0.008412673,0.000104610685,0.000030341122,0.000024696232,0.000033101518,0.0035439767],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99708885,0.0002558589,0.0011964114,0.00059364823,0.0002680694,0.0005971534],"domain_scores_gemma":[0.9975377,0.0011585699,0.00018232921,0.0006165843,0.000101812744,0.00040304862],"candidate_categories":["metaepi_narrow","insufficient_payload"],"consensus_categories":[],"category_scores_codex":[0.0007979521,0.00034423196,0.0013300447,0.0001583644,0.000113410155,0.00003302003,0.00016850609,0.0003681304,0.00073201396],"category_scores_gemma":[0.0014433991,0.00028449946,0.00026927245,0.0001816788,0.00069142226,0.000112978945,0.00016705372,0.0005813864,0.00094497995],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0014670837,0.003239676,0.80846775,0.0010197356,0.0018290926,0.04194179,0.0016404865,0.000001547622,0.0010486834,0.0029118403,0.018965658,0.11746665],"study_design_scores_gemma":[0.002238431,0.0034886205,0.97208315,0.00012522678,0.00030774425,0.01510211,0.00015975311,0.000041968317,0.000010264956,0.0021503253,0.003995984,0.00029640828],"about_ca_topic_score_codex":0.000012833237,"about_ca_topic_score_gemma":0.000011978202,"teacher_disagreement_score":0.16361542,"about_ca_system_score_codex":0.00003771088,"about_ca_system_score_gemma":0.0000706404,"threshold_uncertainty_score":0.9999607},"labels":[],"label_agreement":null},{"id":"W2063829874","doi":"10.1097/mcd.0b013e32834e9290","title":"Correspondence","year":2011,"lang":"en","type":"letter","venue":"Clinical Dysmorphology","topic":"Cardiac, Anesthesia and Surgical Outcomes","field":"Medicine","cited_by":0,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Mount Sinai Hospital; McMaster University; McMaster Children's Hospital; Memorial University of Newfoundland; SickKids Foundation; Hospital for Sick Children","funders":"","keywords":"Medicine","score_opus":0.11938971656551826,"score_gpt":0.38201135515872775,"score_spread":0.26262163859320947,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2063829874","genre_codex":"commentary","genre_gemma":"commentary","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"commentary","genre_consensus":"commentary","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.0044131223,0.0006843282,0.0000711271,0.800821,0.005259591,0.00059663586,0.000024607858,0.00023313207,0.18789648],"genre_scores_gemma":[0.00029072628,0.00028833977,0.000425043,0.7737456,0.0058957706,0.000027100485,0.0002337812,0.00007148274,0.21902215],"study_design_codex":"not_applicable","study_design_gemma":"not_applicable","domain_scores_codex":[0.996092,0.00074804126,0.0011916925,0.0009211367,0.0003817363,0.000665354],"domain_scores_gemma":[0.9932502,0.00485919,0.00029606652,0.0011844662,0.00014492315,0.00026514343],"candidate_categories":["metaepi_narrow","research_integrity","insufficient_payload"],"consensus_categories":["research_integrity","insufficient_payload"],"category_scores_codex":[0.0010496771,0.00042944314,0.0028383378,0.00016914694,0.000044735312,0.000012369995,0.00036277762,0.0035635121,0.013005834],"category_scores_gemma":[0.0023362301,0.00033003985,0.0019762178,0.00015520844,0.00090440514,0.000027071846,0.00013160873,0.004609531,0.009470807],"study_design_candidate":"not_applicable","study_design_consensus":"not_applicable","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0003568587,0.000092026756,0.028885178,0.000059930448,0.00019238275,0.04474013,0.00001032574,1.0200864e-8,0.00000263106,0.0002700369,0.9229974,0.00239308],"study_design_scores_gemma":[0.0010965681,0.00066687894,0.059873696,0.00006155339,0.0005306583,0.003870602,0.000002386121,0.0000010546217,0.000003804118,0.00010240266,0.9334769,0.0003134741],"about_ca_topic_score_codex":0.00002258031,"about_ca_topic_score_gemma":8.3263035e-7,"teacher_disagreement_score":0.040869527,"about_ca_system_score_codex":0.00003971843,"about_ca_system_score_gemma":0.0002838457,"threshold_uncertainty_score":0.9999152},"labels":[],"label_agreement":null},{"id":"W2063848166","doi":"10.1097/mcd.0b013e3283398730","title":"Fetal alcohol syndrome: a phenocopy of spondylocarpotarsal synostosis syndrome?","year":2010,"lang":"en","type":"article","venue":"Clinical Dysmorphology","topic":"Prenatal Substance Exposure Effects","field":"Medicine","cited_by":1,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Yukon Health and Social Services; University of British Columbia; Rare Disease Foundation; Child and Family Research Institute; Children's & Women's Health Centre of British Columbia","funders":"Michael Smith Health Research BC","keywords":"Medicine; Phenocopy; Fetal alcohol syndrome; Fetus; Pediatrics; Pregnancy; Genetics; Phenotype","score_opus":0.026520552719241624,"score_gpt":0.3400056563311314,"score_spread":0.31348510361188975,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2063848166","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9930054,0.00025008005,0.00015529996,0.0009656215,0.0031488356,0.00081523485,0.000050262457,0.00016994844,0.0014393185],"genre_scores_gemma":[0.99341846,0.000029442823,0.0048198416,0.0009200639,0.00020709273,0.000055502933,0.00007615586,0.000073268166,0.000400158],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9964544,0.0002909427,0.001348862,0.0008264348,0.0004169784,0.00066234637],"domain_scores_gemma":[0.99612236,0.0015361236,0.00039780117,0.0012371325,0.00018528338,0.00052128284],"candidate_categories":["metaepi_narrow","insufficient_payload"],"consensus_categories":[],"category_scores_codex":[0.0014373884,0.00036202883,0.0015238861,0.00020655467,0.00005826653,0.000009004957,0.00046101242,0.00087103556,0.0015562432],"category_scores_gemma":[0.0030515015,0.00031959146,0.0005446764,0.00045173088,0.0012947334,0.00011186336,0.0002317273,0.0017327068,0.0007742498],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0026854617,0.0030629933,0.6784018,0.00038072182,0.0010189506,0.024315765,0.00011852775,0.000002253665,0.26197076,0.0022263795,0.007162639,0.01865371],"study_design_scores_gemma":[0.006435867,0.0044951527,0.9528147,0.00015143334,0.00042166657,0.024066003,0.000017187062,0.00009267926,0.0069369874,0.00045605778,0.0037002456,0.00041199924],"about_ca_topic_score_codex":0.000035921676,"about_ca_topic_score_gemma":0.000028452563,"teacher_disagreement_score":0.27441287,"about_ca_system_score_codex":0.00003305008,"about_ca_system_score_gemma":0.00022006835,"threshold_uncertainty_score":0.9999256},"labels":[],"label_agreement":null},{"id":"W2068294067","doi":"10.1097/mcd.0b013e3282f4a10e","title":"Localized acalvaria with craniosynostosis","year":2008,"lang":"en","type":"article","venue":"Clinical Dysmorphology","topic":"Craniofacial Disorders and Treatments","field":"Biochemistry, Genetics and Molecular Biology","cited_by":3,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of British Columbia; BC Children's Hospital","funders":"","keywords":"Medicine; Craniosynostosis; Skull; Presentation (obstetrics); Anatomy; Craniosynostoses; Pathology; Radiology","score_opus":0.03210955766171998,"score_gpt":0.3116664154467303,"score_spread":0.2795568577850103,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2068294067","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.992936,0.00020566174,0.0029778343,0.00036083706,0.00025153413,0.00018173603,0.000019018542,0.000027402804,0.0030399892],"genre_scores_gemma":[0.9950882,0.0005097641,0.0012270339,0.0018102619,0.00015651723,0.000023290802,0.00013595322,0.000029438355,0.001019513],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99864596,0.00012329129,0.00033893134,0.0005044321,0.00009588878,0.0002914688],"domain_scores_gemma":[0.9992498,0.00004327735,0.00008618263,0.0004114854,0.00006599847,0.00014323197],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00012523077,0.00018029877,0.00030686372,0.000024397023,0.00012972357,0.0000055808996,0.00018132738,0.00031641548,0.0002119836],"category_scores_gemma":[0.00015133433,0.00014074265,0.0001586035,0.000092843606,0.0005140473,0.0000024239573,0.000085529886,0.00014500866,0.0001750251],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0021512816,0.0015496088,0.9467951,0.000008585521,0.00051999156,0.00061417534,0.000040744486,0.000017920629,0.012983751,0.0004556366,0.027769562,0.0070936377],"study_design_scores_gemma":[0.011401693,0.005059614,0.68412024,0.0000115394705,0.00014911141,0.000847781,0.000038507776,0.000026389416,0.003434945,0.00033925398,0.2938747,0.00069619267],"about_ca_topic_score_codex":0.00003611617,"about_ca_topic_score_gemma":0.00003179569,"teacher_disagreement_score":0.26610515,"about_ca_system_score_codex":0.000005345068,"about_ca_system_score_gemma":0.00008343275,"threshold_uncertainty_score":0.5739318},"labels":[],"label_agreement":null},{"id":"W2071121505","doi":"10.1097/00019605-200404000-00008","title":"Severe hemihypotrophy in a female infant with mosaic Turner syndrome: a variant of Russell???Silver syndrome?","year":2004,"lang":"en","type":"article","venue":"Clinical Dysmorphology","topic":"Genetic Syndromes and Imprinting","field":"Biochemistry, Genetics and Molecular Biology","cited_by":14,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Health Sciences Centre; University of Manitoba","funders":"","keywords":"Medicine; Failure to thrive; Uniparental disomy; Karyotype; Forehead; Dermatology; Anatomy; Pediatrics; Genetics; Chromosome; Biology","score_opus":0.015443451725337043,"score_gpt":0.2720193214719298,"score_spread":0.25657586974659274,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2071121505","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99781543,0.00037013847,0.00045600408,0.00020928978,0.00028113194,0.00032009327,0.000023218558,0.000013905607,0.0005108035],"genre_scores_gemma":[0.9930573,0.00016262832,0.0058277007,0.00047804145,0.000053283242,0.000035315672,0.00006593155,0.000046444886,0.00027333337],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99738497,0.00014841725,0.000950651,0.0007933562,0.00017589125,0.000546731],"domain_scores_gemma":[0.9986248,0.00006854694,0.00029509718,0.0007506166,0.00008785789,0.00017307047],"candidate_categories":["metaepi_narrow"],"consensus_categories":[],"category_scores_codex":[0.00051204464,0.0002971625,0.00070804625,0.000105495084,0.000040290695,0.000012470429,0.00039475568,0.0005119404,0.00012462569],"category_scores_gemma":[0.00024787727,0.00024557643,0.0002140011,0.00029433548,0.00040512162,0.000006344405,0.00028679534,0.0003726049,0.000047244142],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0010558248,0.004143576,0.7960052,0.00039661396,0.0011472057,0.0089445915,0.0005263631,0.0069322386,0.1714952,0.0007417938,0.001011766,0.007599617],"study_design_scores_gemma":[0.009139316,0.0069335606,0.9406074,0.00022348748,0.00012251301,0.0305368,0.0002293104,0.00003764767,0.0066762217,0.000703781,0.0038882026,0.0009017067],"about_ca_topic_score_codex":0.00015512214,"about_ca_topic_score_gemma":0.000065125554,"teacher_disagreement_score":0.16481899,"about_ca_system_score_codex":0.000023604174,"about_ca_system_score_gemma":0.00023883904,"threshold_uncertainty_score":0.99999964},"labels":[],"label_agreement":null},{"id":"W2071776627","doi":"10.1097/mcd.0b013e3283387b21","title":"An uncommon 3.4-Mb interstitial deletion at 3q29","year":2010,"lang":"en","type":"article","venue":"Clinical Dysmorphology","topic":"Genomic variations and chromosomal abnormalities","field":"Biochemistry, Genetics and Molecular Biology","cited_by":2,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"McMaster University Medical Centre; University of Calgary; Alberta Children's Hospital; Hamilton Regional Laboratory Medicine Program; Hamilton Health Sciences","funders":"","keywords":"Medicine; Dermatology","score_opus":0.014484876505399282,"score_gpt":0.3259142038420125,"score_spread":0.3114293273366132,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2071776627","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99465615,0.000025882106,0.00081545755,0.00034295718,0.0017763862,0.00008735643,0.000035122426,0.00002329076,0.0022373777],"genre_scores_gemma":[0.99515915,0.000029418698,0.0012021979,0.0010548746,0.0011369501,0.000015043242,0.0005059172,0.00001922627,0.00087724667],"study_design_codex":"bench_or_experimental","study_design_gemma":"not_applicable","domain_scores_codex":[0.99873704,0.0001478288,0.000409751,0.00040354265,0.000059377147,0.00024245407],"domain_scores_gemma":[0.999117,0.00003754154,0.000108527995,0.0005229648,0.00007258852,0.0001413863],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00037578805,0.00013297192,0.00018277665,0.000027323036,0.00011242008,0.000016869666,0.00027815058,0.0004298178,0.0007264299],"category_scores_gemma":[0.00015069742,0.00012606122,0.00012815568,0.000034925673,0.00028248908,0.000004896083,0.00017640245,0.00026609344,0.0001841298],"study_design_candidate":"bench_or_experimental","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00044216623,0.00045554448,0.15593538,0.000008086785,0.000070923306,0.00003283739,0.000053662337,0.000028921388,0.82308334,0.0037147547,0.010668992,0.005505399],"study_design_scores_gemma":[0.0033235098,0.0050103944,0.3039953,0.000007711534,0.00010147881,0.00078840513,0.00016161463,0.00029724883,0.09562385,0.0018119472,0.5879761,0.00090241403],"about_ca_topic_score_codex":0.000035920075,"about_ca_topic_score_gemma":0.000556119,"teacher_disagreement_score":0.7274595,"about_ca_system_score_codex":0.000010086256,"about_ca_system_score_gemma":0.00005420154,"threshold_uncertainty_score":0.7953898},"labels":[],"label_agreement":null},{"id":"W2072132652","doi":"10.1097/01.mcd.0000065051.36236.e9","title":"Interstitial deletion of chromosome 2p16.2p21","year":2003,"lang":"en","type":"article","venue":"Clinical Dysmorphology","topic":"Genomic variations and chromosomal abnormalities","field":"Biochemistry, Genetics and Molecular Biology","cited_by":9,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Health Sciences Centre; Manitoba Health","funders":"","keywords":"Medicine; Breakpoint; Chromosome; Genetics; Phenotype; Long arm; Deletion syndrome; Gene; Biology","score_opus":0.023323701146869817,"score_gpt":0.30403638174788095,"score_spread":0.2807126806010111,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2072132652","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9913581,0.00021700784,0.0029769652,0.00011319603,0.00074335205,0.00008972385,0.00002643592,0.000008319873,0.004466901],"genre_scores_gemma":[0.99714804,0.00012669824,0.0012935377,0.00037756164,0.0002258964,0.000010236912,0.000094378505,0.000013309803,0.0007103417],"study_design_codex":"bench_or_experimental","study_design_gemma":"not_applicable","domain_scores_codex":[0.99871475,0.00022056593,0.0005238186,0.00028650917,0.000058744474,0.00019564007],"domain_scores_gemma":[0.9993312,0.000044645665,0.00015229228,0.00031319947,0.000090207606,0.0000684856],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0003723108,0.00011029607,0.0002291867,0.000030356716,0.00003993948,0.0000053978856,0.00015207352,0.00026022166,0.00044660212],"category_scores_gemma":[0.00038632491,0.00010635642,0.00016039921,0.000053963115,0.00026214536,0.0000027231345,0.00006708455,0.00011173173,0.000054304022],"study_design_candidate":"bench_or_experimental","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00071862194,0.0017273704,0.20478436,0.00010726245,0.0006119909,0.00007647391,0.00018945069,0.00017887501,0.68597,0.07509326,0.023450071,0.0070922435],"study_design_scores_gemma":[0.006310664,0.006844941,0.08380952,0.00005061843,0.00020930938,0.00086998503,0.00049759453,0.00005650528,0.3875367,0.0057314523,0.506993,0.0010896907],"about_ca_topic_score_codex":0.000008824395,"about_ca_topic_score_gemma":0.000011172066,"teacher_disagreement_score":0.48354295,"about_ca_system_score_codex":0.000008126887,"about_ca_system_score_gemma":0.00009468043,"threshold_uncertainty_score":0.488998},"labels":[],"label_agreement":null},{"id":"W2073100650","doi":"10.1097/01.mcd.0000127466.26888.15","title":"Cenani–Lenz syndactyly in a patient with features of Kabuki syndrome","year":2004,"lang":"en","type":"article","venue":"Clinical Dysmorphology","topic":"Congenital limb and hand anomalies","field":"Biochemistry, Genetics and Molecular Biology","cited_by":7,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Children's Hospital of Winnipeg; University of Manitoba","funders":"Health Canada; Manitoba Health Research Council","keywords":"Syndactyly; Medicine; Phalanx; Anatomy; CLs upper limits; Synostosis; Ophthalmology","score_opus":0.011213593562898905,"score_gpt":0.27383531228700025,"score_spread":0.26262171872410134,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2073100650","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9957834,0.00084122445,0.000036038327,0.00029514893,0.00014972093,0.00014187495,0.000027710808,0.00000752457,0.0027173436],"genre_scores_gemma":[0.99845105,0.00016532555,0.00044387352,0.00047289405,0.000045807214,0.000013209374,0.000054521206,0.000015615222,0.00033768485],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9988452,0.00006509343,0.00041229208,0.00035589468,0.000078061676,0.00024342672],"domain_scores_gemma":[0.999424,0.000037676084,0.00011442601,0.0002922166,0.000053404776,0.00007831134],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00013639919,0.00014085612,0.0003177418,0.00004850459,0.000023272252,0.000005660801,0.0001582287,0.00024256163,0.00003136577],"category_scores_gemma":[0.00011862518,0.00010858403,0.000109693334,0.00009109815,0.00030439018,0.000002937793,0.00010767925,0.00016903544,0.000013151534],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.008615534,0.007984991,0.4717694,0.00030314777,0.0010343925,0.0117851095,0.00075350434,0.00043813564,0.29860777,0.008438096,0.0015310991,0.18873884],"study_design_scores_gemma":[0.008527068,0.0211583,0.8878051,0.00026923057,0.00009778515,0.00510686,0.00031883531,0.000001296912,0.050011218,0.0014052698,0.024428474,0.00087058457],"about_ca_topic_score_codex":0.000018388459,"about_ca_topic_score_gemma":0.00027386195,"teacher_disagreement_score":0.41603568,"about_ca_system_score_codex":0.000007827973,"about_ca_system_score_gemma":0.0001041307,"threshold_uncertainty_score":0.4427928},"labels":[],"label_agreement":null},{"id":"W2074292765","doi":"10.1097/01.mcd.0000065052.36236.32","title":"Another adult with Meier-Gorlin syndrome - insights into the natural history","year":2003,"lang":"en","type":"article","venue":"Clinical Dysmorphology","topic":"Congenital limb and hand anomalies","field":"Biochemistry, Genetics and Molecular Biology","cited_by":19,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of British Columbia; BC Children's Hospital","funders":"","keywords":"Medicine; Microtia; Natural history; Aplasia; Hypoplasia; Craniofacial; Anatomy; Dermatology; Internal medicine","score_opus":0.01460363483457642,"score_gpt":0.2581668068580629,"score_spread":0.2435631720234865,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2074292765","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9800481,0.005786498,0.00011033833,0.00044902845,0.0008616634,0.0001364813,0.0000017273727,0.000017084923,0.012589032],"genre_scores_gemma":[0.9784028,0.00023863374,0.00032642696,0.0049293647,0.00015828705,0.000023218374,0.000031527557,0.00002581313,0.015863933],"study_design_codex":"bench_or_experimental","study_design_gemma":"not_applicable","domain_scores_codex":[0.99863416,0.0002644223,0.00032457436,0.00044019398,0.000088457455,0.00024818062],"domain_scores_gemma":[0.9991796,0.000085004634,0.000098512704,0.00047034692,0.0000953708,0.00007117313],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00020402024,0.0001824947,0.00024681454,0.000026569649,0.00009098041,0.000010088321,0.00025777813,0.00024345923,0.00019385562],"category_scores_gemma":[0.00025009023,0.00010908564,0.00014257453,0.000055984336,0.00070194586,0.0000041315407,0.0000718433,0.00026997848,0.000088499095],"study_design_candidate":"not_applicable","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.006244274,0.0046364963,0.25064933,0.0002175138,0.004134993,0.0038875707,0.0040459014,0.00003322008,0.36900917,0.12506849,0.1096225,0.12245056],"study_design_scores_gemma":[0.0012470536,0.0013408113,0.016491938,0.000008878406,0.000054820244,0.0003687642,0.00010672325,0.0000067158485,0.0026507098,0.0004104802,0.9769999,0.00031321959],"about_ca_topic_score_codex":0.000007515439,"about_ca_topic_score_gemma":0.00027526202,"teacher_disagreement_score":0.8673774,"about_ca_system_score_codex":0.000017658916,"about_ca_system_score_gemma":0.00013660491,"threshold_uncertainty_score":0.44483832},"labels":[],"label_agreement":null},{"id":"W2078322736","doi":"10.1097/mcd.0b013e32827423de","title":"The Walker–Warburg phenotype and genotype among Irish Travellers","year":2008,"lang":"en","type":"article","venue":"Clinical Dysmorphology","topic":"RNA modifications and cancer","field":"Biochemistry, Genetics and Molecular Biology","cited_by":1,"is_retracted":false,"has_abstract":true,"route_ca_aff":false,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"","funders":"Hospital for Sick Children","keywords":"Medicine; Phenotype; Irish; Genotype; Genetics; Gene; Biology","score_opus":0.03873187430884578,"score_gpt":0.3142978790220754,"score_spread":0.2755660047132296,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2078322736","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99331284,0.002456043,0.0005400276,0.0006807904,0.00046153716,0.00013342084,0.000006348632,0.000012249487,0.0023967444],"genre_scores_gemma":[0.9865921,0.0074719046,0.00025483328,0.00083702983,0.0003674905,0.000022582322,0.000030696563,0.000019118845,0.004404233],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9987755,0.00013846108,0.00035800395,0.00040205303,0.00006931773,0.00025667337],"domain_scores_gemma":[0.99912643,0.000099507015,0.00010294183,0.00048142485,0.00007338844,0.00011628894],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00036442117,0.00012219102,0.00016747777,0.000013262187,0.00030940195,0.000012604521,0.00023321701,0.00026402719,0.000048885322],"category_scores_gemma":[0.00022498255,0.00008906262,0.00009685105,0.0000617348,0.0011466973,0.0000025302895,0.000100658755,0.00019172765,0.000041943404],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0009963426,0.00046001974,0.46260643,0.00001587233,0.00046362673,0.000117305055,0.00020268084,0.000065049615,0.057275236,0.0010146217,0.3514851,0.12529774],"study_design_scores_gemma":[0.00072152074,0.00039470618,0.63950133,0.000002225508,0.00002489742,0.000067378336,0.000045527926,0.00006944193,0.0011550363,0.00018132689,0.35764024,0.00019636138],"about_ca_topic_score_codex":0.000023263065,"about_ca_topic_score_gemma":0.00002448782,"teacher_disagreement_score":0.17689492,"about_ca_system_score_codex":0.0000058384953,"about_ca_system_score_gemma":0.000079126236,"threshold_uncertainty_score":0.42250544},"labels":[],"label_agreement":null},{"id":"W2084457922","doi":"10.1097/mcd.0b013e32832b44e1","title":"Phalangeal hypoplasia, mental retardation, agenesis of the corpus callosum, brainstem abnormalities and ectopic grey matter: unique case or newly recognized syndrome?","year":2009,"lang":"en","type":"article","venue":"Clinical Dysmorphology","topic":"Fetal and Pediatric Neurological Disorders","field":"Medicine","cited_by":0,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":true,"ca_institutions":"McMaster University Medical Centre; McMaster University; University of Toronto; Hospital for Sick Children; SickKids Foundation","funders":"","keywords":"Medicine; Agenesis of the corpus callosum; Medical genetics; Corpus callosum; Pediatrics; Hypoplasia; Agenesis; Anatomy; Genetics; Biology","score_opus":0.04160836099857821,"score_gpt":0.3146361519932169,"score_spread":0.27302779099463864,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2084457922","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9838822,0.00031047018,0.000011184036,0.01307127,0.000530108,0.00051331706,0.00005279059,0.000041284085,0.0015873924],"genre_scores_gemma":[0.9855143,0.0004623649,0.00019178241,0.011114955,0.00010542782,0.000010350229,0.000036483623,0.000013209544,0.0025511722],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99779063,0.00052112225,0.00085834315,0.0004106534,0.00014410328,0.0002751337],"domain_scores_gemma":[0.9983609,0.0007863243,0.00025528634,0.00035112505,0.000076550125,0.00016986714],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00042179925,0.0002032649,0.000694227,0.00006334206,0.0001000515,0.000007464596,0.00014856993,0.0002949715,0.00085017696],"category_scores_gemma":[0.0006644797,0.00011787261,0.0001805522,0.00021092343,0.00062777835,0.000053658892,0.00008770486,0.0003511516,0.000034550474],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0032425318,0.00084982545,0.92186993,0.00021512625,0.000192828,0.013035584,0.00035726966,0.0000013985152,0.0007297919,0.00033171807,0.024984943,0.03418903],"study_design_scores_gemma":[0.0047210422,0.0036292602,0.94734555,0.00003338409,0.0002697194,0.03863578,0.00010575275,0.000026123897,0.000076125354,0.0011172841,0.003851323,0.00018863971],"about_ca_topic_score_codex":0.0001796096,"about_ca_topic_score_gemma":0.00009554816,"teacher_disagreement_score":0.034000393,"about_ca_system_score_codex":0.000013955276,"about_ca_system_score_gemma":0.0000648575,"threshold_uncertainty_score":0.9308841},"labels":[],"label_agreement":null},{"id":"W2085077381","doi":"10.1097/mcd.0b013e32832d06f0","title":"X-linked isolated growth hormone deficiency: expanding the phenotypic spectrum of SOX3 polyalanine tract expansions","year":2009,"lang":"en","type":"article","venue":"Clinical Dysmorphology","topic":"Growth Hormone and Insulin-like Growth Factors","field":"Medicine","cited_by":34,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"McGill University Health Centre","funders":"Manchester Biomedical Research Centre; Wellcome Trust","keywords":"Medicine; Phenotype; Growth hormone deficiency; Growth hormone; Broad spectrum; Internal medicine; Endocrinology; Genetics; Hormone; Gene; Biology","score_opus":0.03697350796629838,"score_gpt":0.3281188672203661,"score_spread":0.2911453592540677,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2085077381","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9827929,0.00144261,0.0010502661,0.010277179,0.00060835894,0.0005564585,0.00001798032,0.00016003149,0.0030941719],"genre_scores_gemma":[0.9941516,0.00080027897,0.00035854857,0.0038789732,0.00040792063,0.000009730697,0.000065565284,0.000040608847,0.0002867583],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9961354,0.00028916678,0.0017426835,0.00067769276,0.00036621228,0.00078882795],"domain_scores_gemma":[0.99726486,0.00085196435,0.000482832,0.0008671059,0.00017462109,0.00035861038],"candidate_categories":["metaepi_narrow"],"consensus_categories":[],"category_scores_codex":[0.0010127329,0.00038505375,0.001165058,0.00024297732,0.00021809772,0.000015799511,0.00046062752,0.00057764363,0.0002859152],"category_scores_gemma":[0.0013680692,0.00025566114,0.000517981,0.0007870644,0.0006590135,0.00012380227,0.000092587055,0.0012366725,0.00016734068],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.007749727,0.013666817,0.44178063,0.0001272602,0.00066111406,0.0015900956,0.0027508873,0.000013984202,0.44988436,0.020370686,0.035947956,0.025456475],"study_design_scores_gemma":[0.003924916,0.006919907,0.9806297,0.000045685756,0.00036122533,0.00038616135,0.00019852532,0.00020916635,0.0024448773,0.0039921813,0.0005733429,0.0003143557],"about_ca_topic_score_codex":0.000057670015,"about_ca_topic_score_gemma":0.0000029639089,"teacher_disagreement_score":0.538849,"about_ca_system_score_codex":0.00004878376,"about_ca_system_score_gemma":0.00020887662,"threshold_uncertainty_score":0.99998957},"labels":[],"label_agreement":null},{"id":"W2184207753","doi":"10.1097/mcd.0000000000000108","title":"Incidental finding of paternal UPD15 in a child with a deletion of 11q21–q22.3, presenting with developmental delay, coloboma and characteristic dysmorphic features","year":2015,"lang":"en","type":"article","venue":"Clinical Dysmorphology","topic":"Genomic variations and chromosomal abnormalities","field":"Biochemistry, Genetics and Molecular Biology","cited_by":3,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"B.C. Women's Hospital & Health Centre; Child and Family Research Institute; University of British Columbia","funders":"","keywords":"Medicine; Coloboma; Genetics; Ophthalmology; Biology","score_opus":0.024424058475399572,"score_gpt":0.2742716856660578,"score_spread":0.24984762719065823,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2184207753","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9992363,0.00010789329,0.0001434656,0.000063517764,0.00006614206,0.0001689344,0.000033904667,0.000003880374,0.00017599166],"genre_scores_gemma":[0.99756044,0.000032234257,0.002051441,0.00007062197,0.00006207388,0.000016643682,0.00011995325,0.000014475182,0.00007211441],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9987553,0.00012590861,0.0005094278,0.00029339446,0.00011475429,0.00020121773],"domain_scores_gemma":[0.9993483,0.000039350103,0.000301315,0.00012986075,0.00009977396,0.00008139517],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00037386615,0.00014006557,0.00031745638,0.00006491583,0.000035824793,0.000009297526,0.0001265782,0.0001751611,0.000013371279],"category_scores_gemma":[0.00012808132,0.00011252397,0.000036260724,0.00008224633,0.0003004403,0.000009046917,0.00015604834,0.00015441822,0.0000012788016],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.001015586,0.00021427986,0.9902952,0.000040437993,0.00009852719,0.00017209118,0.00024742627,0.00003970731,0.0074369498,0.00009801497,0.00006172179,0.00028010624],"study_design_scores_gemma":[0.0027105848,0.0018361249,0.98533225,0.00006996548,0.000041977277,0.0038720644,0.00052635017,0.000042157524,0.0051449686,0.000046704434,0.00018715682,0.00018972425],"about_ca_topic_score_codex":0.00013321756,"about_ca_topic_score_gemma":0.00026053737,"teacher_disagreement_score":0.0049629305,"about_ca_system_score_codex":0.000018453455,"about_ca_system_score_gemma":0.0001445194,"threshold_uncertainty_score":0.45885944},"labels":[],"label_agreement":null},{"id":"W2315250652","doi":"10.1097/mcd.0b013e3283590aac","title":"Situs inversus totalis and congenital hypoglossia associated with atrial ectopic bradycardia and normal neurodevelopmental outcome","year":2012,"lang":"en","type":"article","venue":"Clinical Dysmorphology","topic":"Intestinal Malrotation and Obstruction Disorders","field":"Medicine","cited_by":2,"is_retracted":false,"has_abstract":true,"route_ca_aff":false,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"","funders":"Hospital for Sick Children","keywords":"Medicine; Dextrocardia; Situs inversus; Bradycardia; Pediatrics; General hospital; Congenital malformations; Surgery; Internal medicine; Genetics; Pregnancy","score_opus":0.05151721783985587,"score_gpt":0.33271908083764695,"score_spread":0.2812018629977911,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2315250652","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9963375,0.000164157,0.000018112185,0.00076623855,0.0009960937,0.00024554823,0.000011498145,0.000057648318,0.0014032301],"genre_scores_gemma":[0.99672234,0.000021833734,0.0006158465,0.0019803105,0.00023060528,0.0000047076473,0.000047198926,0.000017177576,0.00036000065],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99868095,0.0001441196,0.00046924475,0.00026023661,0.00013268489,0.00031277706],"domain_scores_gemma":[0.9988951,0.0004694842,0.00013338485,0.00010988468,0.0000917154,0.00030042866],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00031286033,0.00015855284,0.00041176507,0.000064070635,0.00008553304,0.000015200152,0.000037958205,0.00018715317,0.00021837653],"category_scores_gemma":[0.0018842842,0.00012991876,0.00008085496,0.00012816458,0.00053455913,0.00010889077,0.0000632789,0.00034678608,0.000034676006],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0005660444,0.00007817421,0.99444157,0.000008135065,0.00013691347,0.00007913308,0.000091200774,2.6789095e-7,0.000041709478,0.00020690841,0.00035183338,0.0039980835],"study_design_scores_gemma":[0.006042801,0.0007366538,0.99054015,0.0000066064763,0.00020229376,0.0009830107,0.00013478077,0.000027469792,0.000013249526,0.00001955905,0.001145745,0.00014770766],"about_ca_topic_score_codex":0.000025776624,"about_ca_topic_score_gemma":0.000020507765,"teacher_disagreement_score":0.0054767565,"about_ca_system_score_codex":0.000026880702,"about_ca_system_score_gemma":0.000059100857,"threshold_uncertainty_score":0.5297933},"labels":[],"label_agreement":null},{"id":"W2318747610","doi":"10.1097/mcd.0b013e328349bdb3","title":"Ectomorphic body habitus, microcephaly, developmental delay with characteristic facial phenotype","year":2011,"lang":"en","type":"article","venue":"Clinical Dysmorphology","topic":"Congenital heart defects research","field":"Biochemistry, Genetics and Molecular Biology","cited_by":0,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":true,"ca_institutions":"McMaster University","funders":"","keywords":"Medicine; Microcephaly; Pediatrics; Family medicine","score_opus":0.052928834959891605,"score_gpt":0.3166646680468326,"score_spread":0.263735833086941,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2318747610","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99425095,0.00016594313,0.00043813625,0.000059297894,0.00031489704,0.00031707872,0.000041981577,0.000031267842,0.0043804166],"genre_scores_gemma":[0.99422073,0.000063005806,0.0029385432,0.0007683996,0.00029598796,0.000042798674,0.00017580517,0.000050573373,0.0014441566],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9977447,0.00023591303,0.00051658746,0.00074807747,0.00016268037,0.000592041],"domain_scores_gemma":[0.99896497,0.00007772663,0.000105173596,0.00040517142,0.00016935705,0.0002775988],"candidate_categories":["insufficient_payload"],"consensus_categories":["insufficient_payload"],"category_scores_codex":[0.00042489122,0.00026169769,0.00038022225,0.000066417626,0.00011588923,0.000017378636,0.00038855063,0.00040623976,0.000986692],"category_scores_gemma":[0.0003390523,0.00022587748,0.0001357855,0.00012818325,0.0006721121,0.000005189116,0.00034290363,0.00040102712,0.0009549764],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0059589744,0.001693758,0.53807825,0.00007036627,0.0006731802,0.002288183,0.00017661971,3.1496177e-7,0.40300158,0.00021564253,0.007432139,0.04041098],"study_design_scores_gemma":[0.0035785409,0.005516011,0.8588034,0.00002308359,0.00010044019,0.0016903414,0.00004001012,0.000016568463,0.03124092,0.00022756278,0.097863466,0.0008996419],"about_ca_topic_score_codex":0.000049693615,"about_ca_topic_score_gemma":0.00020590148,"teacher_disagreement_score":0.37176067,"about_ca_system_score_codex":0.000023959954,"about_ca_system_score_gemma":0.00033348447,"threshold_uncertainty_score":0.99992657},"labels":[],"label_agreement":null},{"id":"W2320499774","doi":"10.1097/mcd.0000000000000034","title":"Hajdu–Cheney syndrome","year":2014,"lang":"en","type":"article","venue":"Clinical Dysmorphology","topic":"Synthesis of heterocyclic compounds","field":"Chemistry","cited_by":30,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Université de Montréal","funders":"","keywords":"Medicine; Classics","score_opus":0.033951586517684,"score_gpt":0.3203613480149011,"score_spread":0.28640976149721714,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2320499774","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9404833,0.00007125525,0.00029127195,0.0014396172,0.0007682076,0.000036058023,0.0000062149143,0.00025908975,0.056645006],"genre_scores_gemma":[0.99382544,0.00001740752,0.001277243,0.0016184344,0.0004896576,0.000022230297,0.000020065327,0.00004677313,0.002682744],"study_design_codex":"observational","study_design_gemma":"not_applicable","domain_scores_codex":[0.9975649,0.00017404064,0.0008852788,0.0006905383,0.00018364732,0.0005015857],"domain_scores_gemma":[0.9957352,0.0026156541,0.00020532022,0.0011436807,0.00004286475,0.00025723156],"candidate_categories":["insufficient_payload"],"consensus_categories":["insufficient_payload"],"category_scores_codex":[0.00078920234,0.00023459586,0.0006595878,0.000049889954,0.000083655555,0.000025211311,0.0007262445,0.0005060326,0.0077808136],"category_scores_gemma":[0.0024069815,0.0002236183,0.00032293392,0.00006418231,0.00045146534,0.000053960455,0.00027112727,0.000539615,0.002810465],"study_design_candidate":"not_applicable","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00041806776,0.0022821617,0.600602,0.00020844224,0.00062690093,0.0012746373,0.000076001954,0.000015306667,0.07429449,0.0058086645,0.07634709,0.23804624],"study_design_scores_gemma":[0.0030815343,0.00038337836,0.14776379,0.00007671608,0.00015441651,0.0022449037,0.00003055344,0.00070192205,0.007751774,0.009797336,0.82703125,0.0009823933],"about_ca_topic_score_codex":0.000017753124,"about_ca_topic_score_gemma":0.000007731433,"teacher_disagreement_score":0.7506842,"about_ca_system_score_codex":0.000033266726,"about_ca_system_score_gemma":0.000029024917,"threshold_uncertainty_score":0.997966},"labels":[],"label_agreement":null},{"id":"W2321427102","doi":"10.1097/mcd.0b013e328353e32e","title":"A new nonsense mutation is associated with dysmorphism in lethal neonatal CPTII deficiency","year":2012,"lang":"en","type":"letter","venue":"Clinical Dysmorphology","topic":"Cardiovascular Issues in Pregnancy","field":"Medicine","cited_by":1,"is_retracted":false,"has_abstract":true,"route_ca_aff":false,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":true,"ca_institutions":"","funders":"","keywords":"Nonsense; Medicine; Nonsense mutation; Facial dysmorphism; Mutation; Genetics; Missense mutation; Gene; Phenotype; Biology","score_opus":0.04507333446467501,"score_gpt":0.3363378440536368,"score_spread":0.2912645095889618,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2321427102","genre_codex":"commentary","genre_gemma":"commentary","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"commentary","genre_consensus":"commentary","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.33695945,0.021406503,0.004443189,0.6123956,0.009971554,0.004428536,0.0003407726,0.00069223106,0.009362196],"genre_scores_gemma":[0.17986101,0.00043998417,0.007730074,0.77618796,0.011527878,0.000175556,0.004463299,0.0006093825,0.019004883],"study_design_codex":"not_applicable","study_design_gemma":"not_applicable","domain_scores_codex":[0.9931722,0.0010875731,0.001808412,0.0015439987,0.0010224382,0.0013653629],"domain_scores_gemma":[0.9951109,0.0018433817,0.00067897566,0.0017306604,0.00027374006,0.00036229653],"candidate_categories":["metaepi_narrow","research_integrity","insufficient_payload"],"consensus_categories":["research_integrity","insufficient_payload"],"category_scores_codex":[0.0017544648,0.000787882,0.0026374832,0.0005213336,0.00006836687,0.000027718093,0.0004670792,0.0043088617,0.0018381827],"category_scores_gemma":[0.0027882461,0.000699083,0.0010860068,0.00069628714,0.00079344615,0.00012268836,0.00025912368,0.0068369713,0.0010834989],"study_design_candidate":"not_applicable","study_design_consensus":"not_applicable","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00042436915,0.00033032894,0.016592,0.00013498413,0.00080063974,0.14004482,0.00045385092,0.0000031018458,0.000009066499,0.000019624491,0.8216524,0.019534824],"study_design_scores_gemma":[0.022558372,0.0031798147,0.13088718,0.0025274572,0.004552093,0.07084406,0.000059086426,0.000052142197,0.00005611,0.00071768963,0.7623958,0.0021702268],"about_ca_topic_score_codex":0.00018406243,"about_ca_topic_score_gemma":0.00005397494,"teacher_disagreement_score":0.16379236,"about_ca_system_score_codex":0.00038600937,"about_ca_system_score_gemma":0.00089262176,"threshold_uncertainty_score":0.9996943},"labels":[],"label_agreement":null},{"id":"W2327405051","doi":"10.1097/mcd.0b013e32834977f1","title":"Blepharophimosis-ptosis-epicanthus inversus syndrome plus","year":2011,"lang":"en","type":"article","venue":"Clinical Dysmorphology","topic":"Parvovirus B19 Infection Studies","field":"Medicine","cited_by":15,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"McMaster University; McMaster University Medical Centre","funders":"","keywords":"Blepharophimosis; Medicine; Ptosis; Ophthalmology","score_opus":0.2828548284218747,"score_gpt":0.40817370308179246,"score_spread":0.12531887465991776,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2327405051","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9557582,0.00028853724,0.00035160102,0.0009373562,0.00249444,0.00037401172,0.000012161687,0.00028689863,0.039496765],"genre_scores_gemma":[0.9904581,0.00042561334,0.0016336777,0.0055201543,0.00026955336,0.00007216102,0.000011980029,0.0000418627,0.0015669195],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9973396,0.00024925696,0.0010007736,0.0006540357,0.00021121479,0.0005451222],"domain_scores_gemma":[0.99805075,0.0004583904,0.00024086058,0.00068518205,0.00016688781,0.0003979182],"candidate_categories":["insufficient_payload"],"consensus_categories":["insufficient_payload"],"category_scores_codex":[0.0006751627,0.00027404143,0.0010829369,0.0001691975,0.00012566305,0.000006157173,0.00020503368,0.00042989102,0.0037575206],"category_scores_gemma":[0.0009959695,0.00023474434,0.00037937262,0.00033811363,0.0011571713,0.00007236597,0.00022962895,0.0007079302,0.00858178],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0020462386,0.0014558485,0.9068695,0.00006936858,0.0010967037,0.004021403,0.00032705403,7.922579e-7,0.00064185984,0.002283005,0.07608119,0.005107077],"study_design_scores_gemma":[0.005615911,0.0014939335,0.930258,0.000037773316,0.000492075,0.00246071,0.00007550429,0.000024124825,0.00044365172,0.00041503587,0.058352992,0.00033032705],"about_ca_topic_score_codex":0.00011884043,"about_ca_topic_score_gemma":0.000015495882,"teacher_disagreement_score":0.037929844,"about_ca_system_score_codex":0.00010064503,"about_ca_system_score_gemma":0.00017525056,"threshold_uncertainty_score":0.99715316},"labels":[],"label_agreement":null},{"id":"W2328608799","doi":"10.1097/mcd.0b013e328361d42f","title":"Syndromic congenital diarrhea because of the SPINT2 mutation showing enterocyte tufting and unique electron microscopy findings","year":2013,"lang":"en","type":"article","venue":"Clinical Dysmorphology","topic":"Digestive system and related health","field":"Biochemistry, Genetics and Molecular Biology","cited_by":16,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Alberta; Stollery Children's Hospital","funders":"Energy Research Institute, Nanyang Technological University","keywords":"Medicine; Enterocyte; Diarrhea; Mutation; Pediatrics; Pathology; Internal medicine; Genetics; Biology; Small intestine; Gene","score_opus":0.015433588649314467,"score_gpt":0.3219506576680109,"score_spread":0.3065170690186964,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2328608799","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99796605,0.0005159557,0.00013916435,0.0003797714,0.00043398986,0.00038499877,0.000008649575,0.000008814324,0.0001625893],"genre_scores_gemma":[0.9987534,0.00019771351,0.00016910608,0.0004619073,0.000079633755,0.000019076128,0.000028554086,0.000018426972,0.00027212704],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9984727,0.00029386766,0.00055272557,0.00034547973,0.000058382797,0.00027686573],"domain_scores_gemma":[0.9992859,0.00012255835,0.00018779002,0.00023762195,0.00008030615,0.00008585024],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00043309422,0.00013449488,0.00026354112,0.000029503206,0.00008815979,0.000013121164,0.00016422177,0.00037885932,0.000022815038],"category_scores_gemma":[0.000401497,0.000098985656,0.000110988534,0.000055333603,0.00034651923,0.0000064878564,0.00013936553,0.00026048798,0.000020538608],"study_design_candidate":"bench_or_experimental","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.000060471073,0.00007508792,0.14786772,0.00004311828,0.00010682611,0.0000079017445,0.000060587623,0.0000037544676,0.85042936,0.0001224838,0.0007331095,0.0004895967],"study_design_scores_gemma":[0.0015670167,0.0016772243,0.6483152,0.00014498693,0.00008769617,0.0005002482,0.000092347094,0.00007229454,0.34568805,0.00017437049,0.0013825758,0.0002980207],"about_ca_topic_score_codex":0.000090244816,"about_ca_topic_score_gemma":0.000020809883,"teacher_disagreement_score":0.50474125,"about_ca_system_score_codex":0.0000147040755,"about_ca_system_score_gemma":0.00008215508,"threshold_uncertainty_score":0.40365177},"labels":[],"label_agreement":null},{"id":"W2332667638","doi":"10.1097/mcd.0000000000000007","title":"The first report of nephrocalcinosis in a patient with a 16q23.1–16q23.3 deletion, global developmental delay, trigonocephaly, and portocaval shunt","year":2013,"lang":"en","type":"article","venue":"Clinical Dysmorphology","topic":"Pediatric Urology and Nephrology Studies","field":"Medicine","cited_by":36,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Hospital for Sick Children","funders":"","keywords":"Medicine; Trigonocephaly; Surgery; Craniosynostosis","score_opus":0.01793277910347102,"score_gpt":0.29329210952790924,"score_spread":0.2753593304244382,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2332667638","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.98765117,0.0010661482,0.00005789674,0.009120893,0.00019706861,0.00069742143,0.000005744078,0.000028733659,0.0011749368],"genre_scores_gemma":[0.9929441,0.00069410994,0.0011521467,0.004842243,0.000086536114,0.0001815631,0.000015467705,0.0000120883315,0.00007174994],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99734247,0.00015519958,0.0013174905,0.00054653315,0.00016976552,0.0004685208],"domain_scores_gemma":[0.99812335,0.0008095111,0.0004008009,0.00030203044,0.00020630246,0.00015800523],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00070159795,0.00023220589,0.0007426242,0.00006997652,0.00018067114,0.0000060566495,0.00013083206,0.00040311523,0.00008732481],"category_scores_gemma":[0.00080606766,0.0001430501,0.0001046966,0.00029317508,0.0017560467,0.000054249984,0.000219459,0.00044557362,0.000050947638],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0015042739,0.00045139305,0.9774578,0.000010973532,0.00038045293,0.003502371,0.0000897347,9.508168e-7,0.0000048505326,0.000117458825,0.009109426,0.0073702754],"study_design_scores_gemma":[0.0030414837,0.0025404233,0.9613965,0.000010404521,0.00022219207,0.016816856,0.0001857719,0.000029263745,0.000009624848,0.00037348844,0.0152316885,0.00014228417],"about_ca_topic_score_codex":0.0002522188,"about_ca_topic_score_gemma":0.00074605935,"teacher_disagreement_score":0.016061319,"about_ca_system_score_codex":0.00006785341,"about_ca_system_score_gemma":0.00028748458,"threshold_uncertainty_score":0.6470227},"labels":[],"label_agreement":null},{"id":"W2337406037","doi":"10.1097/mcd.0000000000000130","title":"A novel de-novo WNT5A mutation in a Chinese patient with Robinow syndrome","year":2016,"lang":"en","type":"article","venue":"Clinical Dysmorphology","topic":"Wnt/β-catenin signaling in development and cancer","field":"Biochemistry, Genetics and Molecular Biology","cited_by":8,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"SickKids Foundation; Hospital for Sick Children; University of Toronto","funders":"","keywords":"Medicine; Mutation; Genetics; Pediatrics; Gene","score_opus":0.013350497087435817,"score_gpt":0.29012781215258754,"score_spread":0.27677731506515174,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2337406037","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9930103,0.00010665558,0.0056388704,0.00054415903,0.00026882955,0.00015863669,0.000011087015,0.000014998024,0.00024647726],"genre_scores_gemma":[0.9959682,0.000054351647,0.0024794785,0.00074281305,0.000071442046,0.00006953056,0.00004069029,0.000023969298,0.00054947933],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99858934,0.000097334145,0.00044360352,0.00045655732,0.000091176764,0.00032201078],"domain_scores_gemma":[0.9993532,0.000096568125,0.0001333455,0.00025346948,0.000071158145,0.000092289265],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00038016122,0.00016184784,0.0002483962,0.000050975876,0.00002827326,0.0000072059097,0.00017800218,0.000281297,0.00011860875],"category_scores_gemma":[0.0003207584,0.00010073849,0.00007135571,0.000119713884,0.00021067284,0.0000048804436,0.0000913582,0.00011737858,0.000046058958],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0011223006,0.0005616248,0.6429242,0.000017742015,0.00012959969,0.0006531183,0.000099722274,0.00007923354,0.33787626,0.00006759527,0.0013883152,0.015080266],"study_design_scores_gemma":[0.011111137,0.0047534695,0.94594866,0.00017764882,0.00004479652,0.005561161,0.00004930572,0.000032510943,0.02000582,0.0007577674,0.010659754,0.00089797867],"about_ca_topic_score_codex":0.000015220757,"about_ca_topic_score_gemma":0.000075152275,"teacher_disagreement_score":0.31787044,"about_ca_system_score_codex":0.000033398846,"about_ca_system_score_gemma":0.00017314494,"threshold_uncertainty_score":0.41079965},"labels":[],"label_agreement":null},{"id":"W2338328727","doi":"10.1097/mcd.0000000000000125","title":"Partial monosomy 1q43 and partial trisomy 20q13.2: a case report","year":2016,"lang":"en","type":"article","venue":"Clinical Dysmorphology","topic":"Genomic variations and chromosomal abnormalities","field":"Biochemistry, Genetics and Molecular Biology","cited_by":0,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":true,"ca_institutions":"McMaster University","funders":"","keywords":"Medicine; Partial Trisomy; Monosomy; Trisomy; Library science; Family medicine; Pediatrics; Genetics; Karyotype; Chromosome; Biology","score_opus":0.02947815658301711,"score_gpt":0.3163382890107707,"score_spread":0.2868601324277536,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2338328727","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99371386,0.00021200944,0.0031565016,0.0014332711,0.0006336721,0.00015452107,0.00005162687,0.000020808613,0.000623725],"genre_scores_gemma":[0.9954725,0.00016135648,0.00055451976,0.00048876344,0.00095196895,0.000046064004,0.00004418469,0.000020033707,0.0022606305],"study_design_codex":"observational","study_design_gemma":"not_applicable","domain_scores_codex":[0.99806327,0.00021518036,0.0007195098,0.0005945613,0.000065132364,0.0003423363],"domain_scores_gemma":[0.99891543,0.00012147655,0.00019610107,0.00050023274,0.00007447854,0.00019228064],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0005211078,0.00017296906,0.00029296835,0.000027175269,0.000111049936,0.000017241378,0.00012470549,0.00035609058,0.00026640922],"category_scores_gemma":[0.00055118604,0.00012512175,0.00014336398,0.000039091305,0.0004074961,0.000006583038,0.00021665891,0.00010992787,0.00006662586],"study_design_candidate":"not_applicable","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0021433993,0.0015396037,0.6031476,0.00005958653,0.0010121008,0.09474432,0.0002201103,0.000012651889,0.15361297,0.009952878,0.05539226,0.078162506],"study_design_scores_gemma":[0.0074740727,0.0026450637,0.03222582,0.000024216211,0.00022702513,0.14793648,0.00018461628,0.00004914305,0.047520146,0.001231033,0.7594823,0.0010000654],"about_ca_topic_score_codex":0.00004146146,"about_ca_topic_score_gemma":0.000022877646,"teacher_disagreement_score":0.70409006,"about_ca_system_score_codex":0.000008504668,"about_ca_system_score_gemma":0.000104902414,"threshold_uncertainty_score":0.5102317},"labels":[],"label_agreement":null},{"id":"W2495326675","doi":"10.1097/mcd.0000000000000143","title":"Rubinstein–Taybi syndrome type 2: report of nine new cases that extend the phenotypic and genotypic spectrum","year":2016,"lang":"en","type":"article","venue":"Clinical Dysmorphology","topic":"Congenital limb and hand anomalies","field":"Biochemistry, Genetics and Molecular Biology","cited_by":74,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"St. Thomas Hospital","funders":"","keywords":"Rubinstein–Taybi syndrome; Microcephaly; Intellectual disability; Medicine; Missense mutation; Exome sequencing; Genetics; Craniofacial; Pediatrics; Phenotype; Dermatology; Biology; Gene; Psychiatry","score_opus":0.04291805356686488,"score_gpt":0.30821828140415514,"score_spread":0.26530022783729024,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2495326675","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9924854,0.0029642277,0.00017189186,0.002077557,0.0005426796,0.000126556,0.00001994421,0.000011356367,0.0016003967],"genre_scores_gemma":[0.9784565,0.0008126999,0.00013349472,0.00040343683,0.00030983388,0.000003532116,0.000024841875,0.00001783574,0.019837841],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9987213,0.00010079851,0.000440015,0.00041750746,0.00007733208,0.0002430325],"domain_scores_gemma":[0.9989182,0.00020627525,0.00018243615,0.00053300883,0.000044801927,0.00011528316],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00031560013,0.00015468778,0.00031201483,0.000026453507,0.000060474173,0.000008946328,0.00020307656,0.00021460676,0.0003262205],"category_scores_gemma":[0.0005334224,0.0000868825,0.000120357705,0.00005865063,0.00057302264,0.0000045953516,0.00023044823,0.00009692503,0.000033718094],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0020547698,0.00050923,0.4887345,0.00006299852,0.00078855763,0.003985135,0.00006641583,0.0000010445636,0.2906696,0.004088939,0.010462782,0.19857603],"study_design_scores_gemma":[0.002533641,0.0047097974,0.7347328,0.000053551154,0.00021460374,0.016171148,0.00006370297,0.0000017414147,0.025756478,0.0027656464,0.21246494,0.0005319131],"about_ca_topic_score_codex":0.000015599304,"about_ca_topic_score_gemma":0.00009567296,"teacher_disagreement_score":0.2649131,"about_ca_system_score_codex":0.000003927799,"about_ca_system_score_gemma":0.00010540941,"threshold_uncertainty_score":0.35718858},"labels":[],"label_agreement":null},{"id":"W2590603583","doi":"10.1097/mcd.0000000000000172","title":"Genitourinary malformations: an under-recognized feature of ectrodactyly, ectodermal dysplasia and cleft lip/palate syndrome","year":2017,"lang":"en","type":"article","venue":"Clinical Dysmorphology","topic":"Urological Disorders and Treatments","field":"Medicine","cited_by":11,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Health Sciences Centre","funders":"","keywords":"Medicine; Ectrodactyly; Genitourinary system; Ectodermal dysplasia; Renal dysplasia; Hypertelorism; Hydronephrosis; Megaureter; Dermatology; Dysplasia; Pediatrics; Urinary system; Anatomy; Pathology","score_opus":0.06722401230120192,"score_gpt":0.3896392058539492,"score_spread":0.3224151935527473,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2590603583","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.98972255,0.00020168535,0.00005497611,0.0072501907,0.00030839664,0.0004120071,0.000038803413,0.000052666746,0.0019587418],"genre_scores_gemma":[0.995799,0.00045141656,0.0014530276,0.001349059,0.00008662369,0.000018637225,0.00011628988,0.000022739478,0.0007032096],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99826413,0.00018040936,0.0005756799,0.0004773866,0.00013721515,0.0003651531],"domain_scores_gemma":[0.9981964,0.00026910938,0.00037726216,0.0007685759,0.00009009636,0.00029853918],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00033886137,0.000230565,0.0008179575,0.000077611534,0.00026701658,0.000029001314,0.00023138823,0.0005483127,0.0003535799],"category_scores_gemma":[0.00047094555,0.0001735428,0.000192727,0.000045869743,0.00076507125,0.00020116472,0.0001971233,0.00053026533,0.00008614968],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0019318203,0.0030347505,0.9777065,0.00008976945,0.00059645646,0.0022185466,0.00005226437,0.0000024285107,0.00055578887,0.00056588236,0.001927051,0.011318725],"study_design_scores_gemma":[0.0061811726,0.0043486054,0.98268896,0.000026977978,0.00035064365,0.0023222181,0.000025518268,0.00015816416,0.000029140869,0.0030329335,0.0006840803,0.00015158804],"about_ca_topic_score_codex":0.000035402918,"about_ca_topic_score_gemma":0.000019906449,"teacher_disagreement_score":0.011167136,"about_ca_system_score_codex":0.000013314897,"about_ca_system_score_gemma":0.00006236658,"threshold_uncertainty_score":0.70768696},"labels":[],"label_agreement":null},{"id":"W2807971899","doi":"10.1097/mcd.0000000000000227","title":"Familial impairment of vocal cord mobility in childhood with clubfoot","year":2018,"lang":"en","type":"article","venue":"Clinical Dysmorphology","topic":"Neurogenetic and Muscular Disorders Research","field":"Medicine","cited_by":0,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of British Columbia; BC Children's Hospital","funders":"BC Children's Hospital; Rare Disease Foundation","keywords":"Medicine; Exome sequencing; Context (archaeology); Clubfoot; Craniofacial; Genetics; Candidate gene; Vocal cord paralysis; Phenotype; Paralysis; Gene; Biology","score_opus":0.0414780750411512,"score_gpt":0.39719829284530694,"score_spread":0.35572021780415575,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2807971899","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9964101,0.000085049505,0.00021933846,0.00071159896,0.00018508479,0.00069192,0.0000063277053,0.000018714632,0.0016718941],"genre_scores_gemma":[0.9980556,0.000078157784,0.00059895153,0.0009390358,0.00015655892,0.00002580184,0.000011333097,0.000017645352,0.000116921874],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.997987,0.0002644372,0.00065224874,0.00047431584,0.0002524254,0.00036960692],"domain_scores_gemma":[0.9988077,0.00022580988,0.000084818064,0.0005360945,0.00015046027,0.00019508143],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00078522484,0.00013026418,0.0005640237,0.00008984215,0.000025129688,0.0000021706471,0.00015490795,0.00020269903,0.00042943115],"category_scores_gemma":[0.0004818973,0.00009529015,0.00014284419,0.00023946418,0.0015703908,0.000013638233,0.00012402762,0.00043915896,0.000077529374],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0042843553,0.0050559384,0.96365166,0.00004246343,0.000079985904,0.0002217834,0.00008329201,8.3699365e-7,0.00087494234,0.00007791289,0.00081042753,0.02481639],"study_design_scores_gemma":[0.005812666,0.016491402,0.9749174,0.000029982535,0.000039290888,0.00012605009,0.00007205631,0.000039492366,0.00084100117,0.00016958897,0.0013768338,0.00008422603],"about_ca_topic_score_codex":0.000079394005,"about_ca_topic_score_gemma":0.00012966881,"teacher_disagreement_score":0.024732163,"about_ca_system_score_codex":0.00002210392,"about_ca_system_score_gemma":0.00030756934,"threshold_uncertainty_score":0.57861704},"labels":[],"label_agreement":null},{"id":"W2830957746","doi":"10.1097/mcd.0000000000000235","title":"A case of diencephalic syndrome presenting with isolated lipodystrophy","year":2018,"lang":"en","type":"article","venue":"Clinical Dysmorphology","topic":"Nuclear Structure and Function","field":"Biochemistry, Genetics and Molecular Biology","cited_by":0,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Health Sciences Centre; St Mary's Hospital Centre","funders":"National Institute for Health and Care Research","keywords":"Medicine; Lipodystrophy; Emaciation; Failure to thrive; Context (archaeology); Differential diagnosis; Pediatrics; Psychiatry; Pathology; Family medicine; Biology","score_opus":0.019335242679214708,"score_gpt":0.3045270300000551,"score_spread":0.2851917873208404,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2830957746","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9969907,0.00004024782,0.0017076774,0.000035686513,0.00038951277,0.00009691947,0.00000705748,0.00001246135,0.0007197283],"genre_scores_gemma":[0.99755013,0.000008564122,0.001692141,0.00021956574,0.0003188993,0.0000033900806,0.000019460711,0.000017082803,0.00017075958],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9989873,0.000084150255,0.00032801804,0.00035303412,0.000048818125,0.00019868491],"domain_scores_gemma":[0.99925816,0.000028133089,0.0001560115,0.00035964788,0.00012650472,0.00007152586],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00016956708,0.000105369225,0.00021122742,0.00003083389,0.00006272363,0.0000056104777,0.00012130714,0.00022990555,0.00012137411],"category_scores_gemma":[0.00011718396,0.000081858336,0.00007803293,0.00010935132,0.00064722187,0.0000030795961,0.00009537386,0.00012640469,0.00002759854],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0058361352,0.0010716785,0.27133003,0.00012123709,0.0012861744,0.01616421,0.0003262955,0.000027297305,0.64439285,0.0012372908,0.01139113,0.046815645],"study_design_scores_gemma":[0.011720751,0.09528563,0.47307566,0.00009172961,0.00078975933,0.28821555,0.0004937434,0.0018374101,0.050137293,0.0022932207,0.073924795,0.0021344598],"about_ca_topic_score_codex":0.000023411327,"about_ca_topic_score_gemma":0.000027896423,"teacher_disagreement_score":0.59425557,"about_ca_system_score_codex":0.0000024565963,"about_ca_system_score_gemma":0.00002874424,"threshold_uncertainty_score":0.3338086},"labels":[],"label_agreement":null},{"id":"W2889330896","doi":"10.1097/mcd.0000000000000242","title":"UBE2A-related X-linked intellectual disability","year":2018,"lang":"en","type":"article","venue":"Clinical Dysmorphology","topic":"Genetics and Neurodevelopmental Disorders","field":"Biochemistry, Genetics and Molecular Biology","cited_by":5,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Manitoba","funders":"National Institute of Neurological Disorders and Stroke; Greenwood Genetic Center Foundation","keywords":"Medicine; Hypertelorism; Intellectual disability; Hypotonia; Palpebral fissure; Dermatology; Pediatrics; Facial dysmorphism; Short stature; Macrocephaly; hirsutism; Anatomy; Genetics; Phenotype; Pathology; Psychiatry","score_opus":0.03257107184461384,"score_gpt":0.33478486853175465,"score_spread":0.3022137966871408,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2889330896","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9935616,0.00012067364,0.00029635968,0.00056787167,0.0012419261,0.00017911721,0.000010427577,0.000028297094,0.0039936784],"genre_scores_gemma":[0.99592507,0.00016929935,0.0005382064,0.0019450419,0.00016433782,0.000012091919,0.000116193565,0.00002864385,0.0011011058],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.99799216,0.00023692052,0.0006160944,0.0007044474,0.00008987525,0.00036048918],"domain_scores_gemma":[0.99901026,0.00011434118,0.00009219027,0.0005354632,0.000093131544,0.00015462787],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00041677724,0.0001885971,0.00025086035,0.00002055494,0.000104901024,0.000011260083,0.000336719,0.0004017085,0.0008453284],"category_scores_gemma":[0.0012796527,0.00017566596,0.00017268151,0.00012895737,0.0017130973,0.0000016923818,0.00033558786,0.00021999142,0.0007060341],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0012201138,0.002006127,0.32185823,0.000022097242,0.00038630646,0.000032565258,0.00027133824,0.000009211431,0.5131023,0.00038251668,0.09778345,0.06292576],"study_design_scores_gemma":[0.0018553723,0.0031864196,0.81149316,0.0000059175604,0.000033533546,0.000054661763,0.0000675143,0.00008874565,0.014751299,0.00119562,0.16678092,0.00048686547],"about_ca_topic_score_codex":0.0000075329144,"about_ca_topic_score_gemma":0.000044293207,"teacher_disagreement_score":0.49835098,"about_ca_system_score_codex":0.000009160786,"about_ca_system_score_gemma":0.000067302724,"threshold_uncertainty_score":0.9255753},"labels":[],"label_agreement":null},{"id":"W2999447367","doi":"10.1097/mcd.0000000000000313","title":"Haploinsufficiency of AKT3 gene causing microcephaly and psychomotor delay in a patient with 1q43q44 microdeletion","year":2020,"lang":"en","type":"article","venue":"Clinical Dysmorphology","topic":"Genomic variations and chromosomal abnormalities","field":"Biochemistry, Genetics and Molecular Biology","cited_by":2,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Pediatric Oncology Group","funders":"","keywords":"Haploinsufficiency; Microcephaly; Medicine; Chromosomal Abnormality; Penetrance; Intellectual disability; Corpus callosum; AKT3; Microdeletion syndrome; Genetics; Gene; Phenotype; Abnormality; Chromosome; Pediatrics; Pathology; Biology; Karyotype","score_opus":0.019568428994296873,"score_gpt":0.26349625168229507,"score_spread":0.2439278226879982,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2999447367","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9966346,0.00047738026,0.0020025105,0.0005303043,0.0000687232,0.00014296347,0.000031208907,0.000005230524,0.00010710149],"genre_scores_gemma":[0.9949351,0.00016418549,0.0036433837,0.0010929004,0.000077249875,0.00000822813,0.00004871163,0.000012974879,0.00001724593],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9988333,0.00009087725,0.00048074045,0.0003688495,0.000051181047,0.00017507933],"domain_scores_gemma":[0.99951965,0.000023355693,0.00015228106,0.00015645957,0.00006750664,0.00008073258],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00013526928,0.00011486475,0.00023394766,0.000028459488,0.000030481218,0.000006475556,0.000077821205,0.00016379758,0.000020882975],"category_scores_gemma":[0.00007105355,0.00010067069,0.000050785005,0.000086846725,0.00019728071,0.0000033649865,0.00008456209,0.00011138094,0.000003362412],"study_design_candidate":"bench_or_experimental","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0009197373,0.00056648,0.12285383,0.000055799075,0.000077853554,0.00013858113,0.00065544434,0.0002559767,0.87085634,0.00017470203,0.00054909085,0.002896164],"study_design_scores_gemma":[0.017027894,0.031193485,0.44689628,0.0001564654,0.00030526833,0.0039797663,0.0020074649,0.0014659673,0.44286692,0.0004423085,0.051530603,0.0021275585],"about_ca_topic_score_codex":0.00003304994,"about_ca_topic_score_gemma":0.000028359229,"teacher_disagreement_score":0.42798942,"about_ca_system_score_codex":0.0000059716676,"about_ca_system_score_gemma":0.000067053676,"threshold_uncertainty_score":0.41052315},"labels":[],"label_agreement":null},{"id":"W3091828407","doi":"10.1097/mcd.0000000000000351","title":"Heterozygous intragenic deletions of FREM1 are not associated with trigonocephaly","year":2020,"lang":"en","type":"article","venue":"Clinical Dysmorphology","topic":"Craniofacial Disorders and Treatments","field":"Biochemistry, Genetics and Molecular Biology","cited_by":3,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":true,"ca_institutions":"University of Manitoba; Manitoba Health","funders":"","keywords":"Medicine; Trigonocephaly; Genetics; Craniosynostosis; Surgery","score_opus":0.05210759187669222,"score_gpt":0.30766896142477607,"score_spread":0.25556136954808384,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W3091828407","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99727905,0.00016945436,0.00081377453,0.0009982774,0.00011029923,0.00017585044,0.00013490494,0.000018611665,0.0002997507],"genre_scores_gemma":[0.9968897,0.00012874659,0.00017298611,0.0023377284,0.0000923674,0.000013252521,0.00024432494,0.000022563512,0.00009833419],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9987041,0.00014527414,0.00043585701,0.00041458046,0.000081895945,0.00021833759],"domain_scores_gemma":[0.9992174,0.00006180536,0.00023684851,0.00023956136,0.00010117278,0.00014323005],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00011310197,0.00015339867,0.00038496827,0.000017687093,0.00004869172,0.000005633866,0.00017926435,0.00028473188,0.00010415583],"category_scores_gemma":[0.00059279124,0.0001295545,0.00019002889,0.00011858597,0.0002832228,0.0000021922942,0.00007799192,0.00015469335,0.000030537023],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0049670464,0.0050252527,0.8278994,0.000060513168,0.0031073785,0.0006915304,0.0002105801,0.00020240793,0.1220534,0.00029647726,0.018645044,0.016840998],"study_design_scores_gemma":[0.013303584,0.011131514,0.9419103,0.000036865255,0.0004982188,0.00006953588,0.00015590101,0.00013073966,0.015849868,0.00018337776,0.015983881,0.0007461781],"about_ca_topic_score_codex":0.000012666535,"about_ca_topic_score_gemma":0.000069901515,"teacher_disagreement_score":0.11401096,"about_ca_system_score_codex":0.000006061895,"about_ca_system_score_gemma":0.000059398473,"threshold_uncertainty_score":0.5283079},"labels":[],"label_agreement":null},{"id":"W3097427168","doi":"10.1097/mcd.0000000000000354","title":"Female congenital aphallia: a unique case of congenital absence of the clitoris with an ectopic labium majorum","year":2020,"lang":"en","type":"review","venue":"Clinical Dysmorphology","topic":"Sexual Differentiation and Disorders","field":"Biochemistry, Genetics and Molecular Biology","cited_by":0,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Manitoba","funders":"","keywords":"Clitoris; Medicine; External genitalia; Agenesis; Anatomy","score_opus":0.06157812609822726,"score_gpt":0.38547571122933977,"score_spread":0.3238975851311125,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W3097427168","genre_codex":"review","genre_gemma":"review","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"review","genre_consensus":"review","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.23511826,0.7608556,0.00014640299,0.00005425516,0.0017111961,0.0010967838,0.0005662264,0.000018282008,0.00043297972],"genre_scores_gemma":[0.22632404,0.77066,0.00029124366,0.00040332935,0.00053477485,0.00008946499,0.0009435421,0.00009526334,0.00065838173],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.99716157,0.00073905743,0.0010719859,0.0006669452,0.000115100716,0.00024536622],"domain_scores_gemma":[0.9979122,0.00018845132,0.0007313502,0.0008430144,0.00017021182,0.00015475863],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0002462459,0.00033949944,0.0012905423,0.00003838113,0.00004473609,0.000008706567,0.0005356475,0.0007808028,0.000088239685],"category_scores_gemma":[0.0004922219,0.00022359498,0.0005066932,0.00019806958,0.00080169464,0.0000039238976,0.0002722994,0.00041700937,0.000010576357],"study_design_candidate":"not_applicable","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0016627535,0.0047961124,0.03671751,0.013831225,0.007397111,0.0033976205,0.000443227,0.0000038372796,0.0012354135,0.0035529544,0.0045979745,0.92236423],"study_design_scores_gemma":[0.0021214026,0.0046828706,0.0014741112,0.00036192266,0.001446877,0.0022984305,0.00039581113,0.000007190092,0.00032585274,0.00005947994,0.98606324,0.00076280994],"about_ca_topic_score_codex":0.00005598845,"about_ca_topic_score_gemma":0.00026896255,"teacher_disagreement_score":0.9814653,"about_ca_system_score_codex":0.000009165148,"about_ca_system_score_gemma":0.00043636365,"threshold_uncertainty_score":0.9117939},"labels":[],"label_agreement":null},{"id":"W3194537089","doi":"10.1097/mcd.0000000000000382","title":"Clinical and molecular characterization of an almost complete ring chromosome 4 in two sisters, with recurrence due to gonadal mosaicism","year":2021,"lang":"en","type":"article","venue":"Clinical Dysmorphology","topic":"Genomic variations and chromosomal abnormalities","field":"Biochemistry, Genetics and Molecular Biology","cited_by":2,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of British Columbia; Alberta Children's Hospital; University of Alberta; University of Calgary","funders":"","keywords":"Medicine; Ring chromosome; Genetics; Chromosome; Karyotype; Gene; Biology","score_opus":0.02552254320334941,"score_gpt":0.3193714900185117,"score_spread":0.29384894681516227,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W3194537089","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9962104,0.000071733695,0.0026467992,0.0004287658,0.00023493306,0.00015331812,0.00013141838,0.000005883958,0.0001167761],"genre_scores_gemma":[0.99359965,0.000060566672,0.0042083194,0.0010180671,0.00014510725,0.000015686144,0.00087133003,0.000017997221,0.00006327405],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.99790084,0.0004133385,0.00077707315,0.00059264735,0.00008382758,0.000232245],"domain_scores_gemma":[0.99904823,0.00006692834,0.00016870635,0.0004283025,0.0001358074,0.00015201759],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0004964476,0.00015066694,0.0004287764,0.000037237678,0.000038325405,0.000015835261,0.00016971829,0.00016799866,0.00003221449],"category_scores_gemma":[0.00021757671,0.00014815906,0.000067374,0.00012836936,0.0002751379,0.000009157618,0.00021966573,0.00018160668,0.0000046903015],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00043251304,0.0005997447,0.1897042,0.000043293687,0.00010099909,0.0012664701,0.00010228463,0.000079525074,0.7997784,0.0011801495,0.00002310917,0.0066893096],"study_design_scores_gemma":[0.0042488105,0.0024637403,0.9383229,0.00009811064,0.00006919502,0.0019514022,0.0001625198,0.00028109015,0.04377269,0.00035557774,0.007690069,0.00058387575],"about_ca_topic_score_codex":0.00003352965,"about_ca_topic_score_gemma":0.00018747094,"teacher_disagreement_score":0.7560057,"about_ca_system_score_codex":0.000007174915,"about_ca_system_score_gemma":0.00013820393,"threshold_uncertainty_score":0.6041751},"labels":[],"label_agreement":null},{"id":"W3206200314","doi":"10.1097/mcd.0000000000000397","title":"Biallelic DNAJC3 variants in a neuroendocrine developmental disorder with insulin dysregulation","year":2021,"lang":"en","type":"article","venue":"Clinical Dysmorphology","topic":"Endoplasmic Reticulum Stress and Disease","field":"Biochemistry, Genetics and Molecular Biology","cited_by":8,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Surrey Place Centre","funders":"","keywords":"Phenotype; Unfolded protein response; Mutation; Endoplasmic reticulum; Gene; Diabetes mellitus; Exon; Loss function","score_opus":0.01704694659813894,"score_gpt":0.29538538306823287,"score_spread":0.27833843647009393,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W3206200314","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9968715,0.00032047255,0.0003792437,0.0006621262,0.00021137565,0.00012956455,0.00001733333,0.000011798122,0.0013966345],"genre_scores_gemma":[0.9957921,0.0004200896,0.0015083788,0.0012287087,0.00012059421,0.000028140972,0.00037614733,0.00002249606,0.0005033395],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9983524,0.00021977167,0.00045961523,0.00058019673,0.00009697995,0.0002910249],"domain_scores_gemma":[0.9993745,0.00005822901,0.00008514381,0.00028576,0.000066381195,0.00012996708],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00011049124,0.00015878161,0.0002524042,0.000037509508,0.000040629064,0.0000144441,0.00012986564,0.00011231033,0.00020400686],"category_scores_gemma":[0.0004879434,0.00014029715,0.00007603104,0.00015781708,0.00016757961,0.0000044404555,0.00016910065,0.00016420663,0.00004052364],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00088132586,0.0011506097,0.96258503,0.000023739829,0.00008261124,0.0024517744,0.000018641078,0.00025355056,0.018470004,0.00050637353,0.0015736931,0.012002666],"study_design_scores_gemma":[0.004780164,0.00042255112,0.9636112,0.000019003326,0.000023532097,0.0005491244,0.00006010027,0.00009532217,0.0036965532,0.00013930383,0.026333293,0.00026987717],"about_ca_topic_score_codex":0.000017408922,"about_ca_topic_score_gemma":0.00041092854,"teacher_disagreement_score":0.0247596,"about_ca_system_score_codex":0.000010191275,"about_ca_system_score_gemma":0.00024489174,"threshold_uncertainty_score":0.5721152},"labels":[],"label_agreement":null},{"id":"W4233357937","doi":"10.1097/00019605-200307000-00007","title":"Interstitial deletion of chromosome 2p16.2p21","year":2003,"lang":"en","type":"article","venue":"Clinical Dysmorphology","topic":"Genomic variations and chromosomal abnormalities","field":"Biochemistry, Genetics and Molecular Biology","cited_by":1,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Manitoba; Health Sciences Centre; Manitoba Health","funders":"","keywords":"Medicine; Chromosome; Genetics; Breakpoint; Phenotype; Long arm; Deletion syndrome; Gene; Biology","score_opus":0.023323701146869817,"score_gpt":0.30403638174788095,"score_spread":0.2807126806010111,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4233357937","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9913581,0.00021700784,0.0029769652,0.00011319603,0.00074335205,0.00008972385,0.00002643592,0.000008319873,0.004466901],"genre_scores_gemma":[0.99714804,0.00012669824,0.0012935377,0.00037756164,0.0002258964,0.000010236912,0.000094378505,0.000013309803,0.0007103417],"study_design_codex":"bench_or_experimental","study_design_gemma":"not_applicable","domain_scores_codex":[0.99871475,0.00022056593,0.0005238186,0.00028650917,0.000058744474,0.00019564007],"domain_scores_gemma":[0.9993312,0.000044645665,0.00015229228,0.00031319947,0.000090207606,0.0000684856],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0003723108,0.00011029607,0.0002291867,0.000030356716,0.00003993948,0.0000053978856,0.00015207352,0.00026022166,0.00044660212],"category_scores_gemma":[0.00038632491,0.00010635642,0.00016039921,0.000053963115,0.00026214536,0.0000027231345,0.00006708455,0.00011173173,0.000054304022],"study_design_candidate":"bench_or_experimental","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00071862194,0.0017273704,0.20478436,0.00010726245,0.0006119909,0.00007647391,0.00018945069,0.00017887501,0.68597,0.07509326,0.023450071,0.0070922435],"study_design_scores_gemma":[0.006310664,0.006844941,0.08380952,0.00005061843,0.00020930938,0.00086998503,0.00049759453,0.00005650528,0.3875367,0.0057314523,0.506993,0.0010896907],"about_ca_topic_score_codex":0.000008824395,"about_ca_topic_score_gemma":0.000011172066,"teacher_disagreement_score":0.48354295,"about_ca_system_score_codex":0.000008126887,"about_ca_system_score_gemma":0.00009468043,"threshold_uncertainty_score":0.488998},"labels":[],"label_agreement":null},{"id":"W4311154940","doi":"10.1097/mcd.0000000000000438","title":"Novel FREM1 homozygous variant in an individual with an intermediate phenotype between Bifid Nose with or without Anorectal and Renal Anomalies and Manitoba-oculo-tricho-anal syndromes","year":2022,"lang":"en","type":"article","venue":"Clinical Dysmorphology","topic":"Ocular Disorders and Treatments","field":"Biochemistry, Genetics and Molecular Biology","cited_by":6,"is_retracted":false,"has_abstract":true,"route_ca_aff":false,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":true,"ca_institutions":"","funders":"","keywords":"Medicine; Phenotype; Nose; Anatomy; Genetics; Gene; Biology","score_opus":0.04059812032415588,"score_gpt":0.3131985016794367,"score_spread":0.2726003813552808,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4311154940","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99865586,0.00036077344,0.00017294388,0.00007380295,0.00008208318,0.00033926487,0.00026304647,0.000017380908,0.00003482164],"genre_scores_gemma":[0.99619216,0.00007829068,0.0023658925,0.00028946798,0.00012627963,0.00006241996,0.0007822509,0.000046572564,0.00005666968],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99778503,0.0003407145,0.00042030978,0.0008842416,0.00017860596,0.00039108514],"domain_scores_gemma":[0.9990989,0.00006974551,0.0001783722,0.00038611787,0.00004457721,0.00022231588],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00040594363,0.00030063966,0.00054058124,0.00012152458,0.00017892443,0.000051760253,0.00026559472,0.0002037159,0.00003558147],"category_scores_gemma":[0.000045307384,0.00021793458,0.00004394664,0.00017395633,0.00057106966,0.000022343978,0.00037129546,0.00035491734,0.0000014058925],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0027035524,0.0009965508,0.9854805,0.0000122299225,0.00040709603,0.0013707302,0.00016904197,0.000012610984,0.0009166017,0.000015080985,0.000031997875,0.0078840135],"study_design_scores_gemma":[0.0075851157,0.023868788,0.9639043,0.000013059904,0.0002972109,0.002406676,0.00067173777,0.00006894163,0.0001034828,0.00007236222,0.0005487868,0.00045953106],"about_ca_topic_score_codex":0.00025094196,"about_ca_topic_score_gemma":0.0033557953,"teacher_disagreement_score":0.022872237,"about_ca_system_score_codex":0.00001584857,"about_ca_system_score_gemma":0.00015959809,"threshold_uncertainty_score":0.8887114},"labels":[],"label_agreement":null},{"id":"W4323294333","doi":"10.1097/mcd.0000000000000455","title":"The PHF21A neurodevelopmental disorder: an evaluation of clinical data from 13 patients","year":2023,"lang":"en","type":"article","venue":"Clinical Dysmorphology","topic":"Genomic variations and chromosomal abnormalities","field":"Biochemistry, Genetics and Molecular Biology","cited_by":5,"is_retracted":false,"has_abstract":true,"route_ca_aff":false,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"","funders":"Institute of Genetics; Medical Research Council; National Institute for Health and Care Research","keywords":"Intellectual disability; Medicine; Hypotonia; Neurodevelopmental disorder; Phenotype; Genetics; Autism; Psychiatry; Pediatrics; Gene; Biology","score_opus":0.15872759996944805,"score_gpt":0.4209666335025531,"score_spread":0.26223903353310507,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4323294333","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"codex-gemma-dda1882f352a","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99716586,0.00011029969,0.000045273366,0.00023151159,0.0015357167,0.0002160634,0.00041554734,0.000015143828,0.00026458723],"genre_scores_gemma":[0.9910184,0.00047235843,0.00019200252,0.00025845025,0.0003697572,0.00001911398,0.007484702,0.00001709661,0.00016807769],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99691194,0.000987645,0.0010687946,0.000574579,0.0002339241,0.0002231168],"domain_scores_gemma":[0.99791837,0.00034523208,0.00030056745,0.0011296346,0.00022233023,0.000083872306],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0033156811,0.00011915831,0.0002497691,0.000019532545,0.0001439559,0.000016298054,0.00078474556,0.00024154337,0.00010870489],"category_scores_gemma":[0.0020501625,0.00009095101,0.000099929144,0.00009309427,0.00033033604,0.000009368231,0.00073767686,0.00016009757,0.00011166283],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00015891813,0.00038694192,0.9375789,0.0000022677564,0.00011351799,0.0000014356913,0.000028323933,0.00004448242,0.000374431,0.000050787163,0.011668113,0.04959185],"study_design_scores_gemma":[0.0015703795,0.000454672,0.96324223,0.000002278855,0.0000653908,0.0000012772922,0.00012939498,0.0018167979,0.00011149962,0.00048913516,0.0320024,0.0001145576],"about_ca_topic_score_codex":0.000071634575,"about_ca_topic_score_gemma":0.00030718558,"teacher_disagreement_score":0.049477294,"about_ca_system_score_codex":0.0000049149694,"about_ca_system_score_gemma":0.00022955931,"threshold_uncertainty_score":0.37088746},"labels":[],"label_agreement":null}]}