{"meta":{"query_hash":"a28d12dea27f","filters":{"venue":"Neurology Genetics"},"cohort_total":89,"direct_labels_cover":0,"predictions_cover":89,"exported":89,"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/a28d12dea27f","api":"https://metacan.xera.ac/api/v1/cohort?venue=Neurology+Genetics"},"results":[{"id":"W2180140742","doi":"10.1212/nxg.0000000000000028","title":"Two definite cases of sudden unexpected death in epilepsy in a family with a <i>DEPDC5</i> mutation","year":2015,"lang":"en","type":"article","venue":"Neurology Genetics","topic":"Epilepsy research and treatment","field":"Medicine","cited_by":58,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Université de Montréal; Hospital for Sick Children","funders":"UCB Pharma; Genome Canada; Canadian Institutes of Health Research; University of Toronto; Savoy Foundation; Ontario Brain Institute","keywords":"Epilepsy; Mutation; Temporal lobe; Sudden death; Epilepsy syndromes; Medicine; Neuroscience; Computer science; Cardiology; Psychology; Biology; Genetics; Gene","score_opus":0.05700888667769597,"score_gpt":0.32274785359498265,"score_spread":0.26573896691728666,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2180140742","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9904359,0.0011368778,0.0018763164,0.0010061167,0.00017741004,0.00015385366,0.00022154315,0.00007050493,0.0049213246],"genre_scores_gemma":[0.9967872,0.00038746357,0.0009118086,0.0004504964,0.00023905408,0.0000435926,0.0001556412,0.000018531096,0.0010062042],"study_design_codex":"case_report","study_design_gemma":"case_report","domain_scores_codex":[0.9993272,0.00010557171,0.00008314837,0.00020038137,0.00009387056,0.00018986552],"domain_scores_gemma":[0.99813604,0.00059277733,0.0004549542,0.00011916015,0.00013738524,0.0005596085],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0006009363,0.001776116,0.0007570801,0.0013874117,0.0022165363,0.0007913803,0.0012206173,0.0031188873,0.0017749092],"category_scores_gemma":[0.003487439,0.00089539593,0.0009722025,0.0006517174,0.00174303,0.00078421674,0.0015673237,0.0013698576,0.0004971888],"study_design_candidate":"case_report","study_design_consensus":"case_report","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00006182825,0.00007703806,0.019759733,0.000021681351,0.0000133936055,0.97700137,0.0003884084,0.00007868863,0.0008104964,0.00019928713,0.0003369836,0.001250979],"study_design_scores_gemma":[0.000030236351,0.00016374496,0.018205246,0.000013796882,0.0000206089,0.97984856,0.0001441981,0.00015221773,0.00052961084,0.00019868658,0.0006732056,0.000019876019],"about_ca_topic_score_codex":0.0024620078,"about_ca_topic_score_gemma":0.0029580505,"teacher_disagreement_score":0.0031188873,"about_ca_system_score_codex":0.0009386248,"about_ca_system_score_gemma":0.0005697297,"threshold_uncertainty_score":0.006810248},"labels":[],"label_agreement":null},{"id":"W2221162814","doi":"10.1212/nxg.0000000000000010","title":"Genetic analysis for a shared biological basis between migraine and coronary artery disease","year":2015,"lang":"en","type":"article","venue":"Neurology Genetics","topic":"Migraine and Headache Studies","field":"Medicine","cited_by":74,"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; National Institute of Neurological Disorders and Stroke; National Cancer Institute; National Institute of Mental Health; National Heart, Lung, and Blood Institute; National Institute on Alcohol Abuse and Alcoholism; Universitätsmedizin der Johannes Gutenberg-Universität Mainz; Universitätsklinikum Hamburg-Eppendorf; National Institutes of Health; King's College London; Academy of Finland; Terveyden ja hyvinvoinnin laitos; Helsingin ja Uudenmaan Sairaanhoitopiiri; Turun Yliopistollinen Keskussairaala; Centre for Medical Systems Biology; Université de Bordeaux; Suomen Kulttuurirahasto; Oulun Yliopisto; Turun Yliopisto; University of Pennsylvania; Medizinische Universität Graz; Emil Aaltosen Säätiö; Deutsche Forschungsgemeinschaft; Nederlandse Organisatie voor Wetenschappelijk Onderzoek; Technische Universität München; Tampereen Yliopisto; Juho Vainion Säätiö; Avera Institute for Human Genetics; Háskóli Íslands; Bundesministerium für Bildung und Forschung; Samfundet Folkhälsan; Universität zu Lübeck; Queensland University of Technology; Eberhard Karls Universität Tübingen; Universiteit Leiden; School of Medicine, Stanford University; Institut National de la Santé et de la Recherche Médicale; Karl-Franzens-Universität Graz; University of Bristol; Universität Heidelberg; Vrije Universiteit Amsterdam; University of Ottawa; Deutsches Zentrum für Herz-Kreislaufforschung; FP7 Health; Imperial College London; Biocenter, University of Oulu; National Institute for Health and Care Research; Folkhälsanin Tutkimussäätiö; European Commission; Norges Teknisk-Naturvitenskapelige Universitet; Tampereen Tuberkuloosisäätiö; Kela; University of Leeds; Medical Research Council; Institute for Translational Medicine and Therapeutics; Wellcome Trust; Paavo Nurmen Säätiö; ZonMw; Amgen","keywords":"Migraine; Aura; Genome-wide association study; Migraine with aura; Coronary artery disease; Genetic association; Genetics; Disease; Bioinformatics; Biology; Medicine; Internal medicine; Single-nucleotide polymorphism; Gene; Genotype","score_opus":0.09739641003695221,"score_gpt":0.314002861507211,"score_spread":0.2166064514702588,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2221162814","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99559575,0.0004519842,0.0032063858,0.00018414321,0.000007605226,0.000018357816,0.00015321243,0.000021768348,0.00036074469],"genre_scores_gemma":[0.9973226,0.000105333114,0.002327872,0.00003119621,0.000019407575,0.000011986024,0.00012578118,0.0000051493857,0.000050737766],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9970715,0.0013363804,0.00022759548,0.0006556356,0.0005341401,0.00017470565],"domain_scores_gemma":[0.99390715,0.0034213634,0.0016017426,0.00060889585,0.00022264848,0.00023817747],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0032428685,0.0005471673,0.0005239145,0.0016603187,0.0004313993,0.0006209671,0.00052691385,0.00057717646,0.0018382401],"category_scores_gemma":[0.0098049175,0.000219295,0.0008417961,0.0013799223,0.00089244,0.0003038047,0.0011348813,0.00053615833,0.00011013692],"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":[0.00079542946,0.00010215275,0.9610267,0.00008618925,0.001975535,0.0009112124,0.00021977755,0.001004538,0.020019626,0.00057101774,0.00015342052,0.0131344795],"study_design_scores_gemma":[0.00008659958,0.000278698,0.9917999,0.000020614883,0.0005159892,0.0015260136,0.00010708827,0.0029607043,0.0016348521,0.000799088,0.00025742405,0.000013042301],"about_ca_topic_score_codex":0.0015755044,"about_ca_topic_score_gemma":0.0015164367,"teacher_disagreement_score":0.0032428685,"about_ca_system_score_codex":0.0002504426,"about_ca_system_score_gemma":0.0005798023,"threshold_uncertainty_score":0.017150104},"labels":[],"label_agreement":null},{"id":"W2223555377","doi":"10.1212/nxg.0000000000000038","title":"Late diagnosis of cerebral folate deficiency: Fewer seizures with folinic acid in adult siblings","year":2015,"lang":"en","type":"article","venue":"Neurology Genetics","topic":"Folate and B Vitamins Research","field":"Medicine","cited_by":16,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Alberta Children's Hospital; Children's Hospital of Eastern Ontario","funders":"Canadian Institutes of Health Research; Ontario Genomics; Ontario Genomics Institute; Genome Canada","keywords":"Medicine; Folinic acid; Pediatrics; Epilepsy; Cerebral palsy; Ataxia; Internal medicine; Chemotherapy; Psychiatry","score_opus":0.03599418747497392,"score_gpt":0.3065103995730386,"score_spread":0.2705162120980647,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2223555377","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9873537,0.0024235526,0.0015504125,0.0026079959,0.00018268949,0.0000603792,0.00029086153,0.00015105246,0.005379299],"genre_scores_gemma":[0.9949033,0.0009716185,0.0011821124,0.00089724426,0.00013733159,0.000016342276,0.00017960834,0.000022248036,0.001690134],"study_design_codex":"case_report","study_design_gemma":"observational","domain_scores_codex":[0.9998337,0.000021456077,0.000024393743,0.000045190063,0.000038528273,0.000036671907],"domain_scores_gemma":[0.99947923,0.00008313001,0.0001306915,0.000022263588,0.000046308513,0.00023836999],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00015888902,0.0006496871,0.00055494014,0.000598919,0.0007083475,0.00029331018,0.00042818417,0.0012341958,0.003179641],"category_scores_gemma":[0.0013906208,0.00018660133,0.00034827972,0.00039496607,0.00031131908,0.0005025747,0.0003659661,0.001035507,0.0005500871],"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":[0.00008001751,0.00012898706,0.049865708,0.000039932842,0.000013949267,0.9360994,0.0003342267,0.000065235436,0.003384554,0.00015805481,0.0009312949,0.008898593],"study_design_scores_gemma":[0.000010529379,0.000206209,0.027609577,0.000024026507,0.000017240562,0.9691544,0.00017306824,0.0001171617,0.0009901979,0.00017702399,0.0015055614,0.0000150537535],"about_ca_topic_score_codex":0.001864603,"about_ca_topic_score_gemma":0.0023874966,"teacher_disagreement_score":0.003179641,"about_ca_system_score_codex":0.00047490338,"about_ca_system_score_gemma":0.0004754732,"threshold_uncertainty_score":0.010636926},"labels":[],"label_agreement":null},{"id":"W2233837568","doi":"10.1212/nxg.0000000000000009","title":"Loss-of-function mutations in <i>RAB39B</i> are associated with typical early-onset Parkinson disease","year":2015,"lang":"en","type":"article","venue":"Neurology Genetics","topic":"Cellular transport and secretion","field":"Biochemistry, Genetics and Molecular Biology","cited_by":93,"is_retracted":false,"has_abstract":true,"route_ca_aff":false,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"","funders":"National Institute on Aging; H. Lundbeck A/S; Medical Research Council; Fondation Roger de Spoelberch; Parkinson Vereniging; Université de Bordeaux; Eberhard Karls Universität Tübingen; Institut National de la Santé et de la Recherche Médicale; GlaxoSmithKline; Deutsches Zentrum für Neurodegenerative Erkrankungen; Centre Hospitalier Universitaire de Bordeaux; Association France Parkinson; Agence Nationale de la Recherche; Centre National de la Recherche Scientifique; Valeant Pharmaceuticals International; FONDATION ALZHEIMER; Michael J. Fox Foundation for Parkinson's Research; Teva Pharmaceutical Industries; National Institutes of Health; U.S. Department of Health and Human Services","keywords":"Missense mutation; Loss function; Rab; Mutation; Genetics; Biology; Guanosine; Gene; Intellectual disability; GTPase; Phenotype","score_opus":0.01479670624108142,"score_gpt":0.2219417735777629,"score_spread":0.20714506733668148,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2233837568","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.991232,0.0006871804,0.0021262867,0.00034157207,0.000067420115,0.0000598792,0.00086386636,0.00021420183,0.0044075255],"genre_scores_gemma":[0.9957189,0.00036727494,0.0011479642,0.00017045051,0.00010069833,0.000020744712,0.0005119597,0.00007368076,0.0018883288],"study_design_codex":"case_report","study_design_gemma":"observational","domain_scores_codex":[0.9997335,0.00003272625,0.000039806404,0.00007744992,0.00008012479,0.000036422454],"domain_scores_gemma":[0.9994673,0.00013650209,0.0001768312,0.000037588477,0.000048862745,0.00013289353],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0002573836,0.0018327667,0.00054593396,0.0010701749,0.000687667,0.00047404523,0.00059913937,0.0010037414,0.004393809],"category_scores_gemma":[0.0008789691,0.00032671195,0.0003160537,0.000573372,0.00093338755,0.00027895338,0.0005636904,0.0006533761,0.0015532958],"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":[0.0015943139,0.00049397803,0.082518905,0.00031950822,0.0002783634,0.48102972,0.001343029,0.0004776024,0.40017936,0.0011435756,0.006499347,0.02412236],"study_design_scores_gemma":[0.00013421816,0.0007218147,0.3327157,0.00008755876,0.00020522563,0.61999655,0.00026444113,0.0007346791,0.03277531,0.0005743818,0.011716152,0.00007392852],"about_ca_topic_score_codex":0.0013075841,"about_ca_topic_score_gemma":0.0015477594,"teacher_disagreement_score":0.004393809,"about_ca_system_score_codex":0.0002372943,"about_ca_system_score_gemma":0.00019483578,"threshold_uncertainty_score":0.014698803},"labels":[],"label_agreement":null},{"id":"W2287264318","doi":"10.1212/nxg.0000000000000043","title":"Co-occurrence of 16p13.11 microdeletion and ring chromosome 20 syndrome","year":2016,"lang":"en","type":"article","venue":"Neurology Genetics","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":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Hospital for Sick Children","funders":"University of Toronto; Eisai; Ontario Brain Institute; Genome Canada","keywords":"Irritability; Mood; Pediatrics; Family history; Girl; Psychology; Mood swing; Psychiatry; Medicine; Developmental psychology; Internal medicine; Cognition","score_opus":0.008332011157793938,"score_gpt":0.21869282153346803,"score_spread":0.21036081037567408,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2287264318","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9942023,0.0006430601,0.00033487126,0.00042349906,0.00005251873,0.00001748993,0.0002897282,0.000053312215,0.0039831665],"genre_scores_gemma":[0.99860686,0.00020545004,0.00020158196,0.000045288063,0.000057208486,0.000004301354,0.000089969224,0.000007367531,0.0007819515],"study_design_codex":"case_report","study_design_gemma":"case_report","domain_scores_codex":[0.9995332,0.000054050088,0.00004985975,0.00016739506,0.00007668284,0.000118816846],"domain_scores_gemma":[0.998818,0.00040613004,0.00032666407,0.00006879835,0.00006282755,0.00031754837],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00017303308,0.00085606007,0.0005764584,0.0016732567,0.00088137813,0.0006045342,0.00062447623,0.0012957575,0.004438436],"category_scores_gemma":[0.0015848149,0.00053281937,0.0002812272,0.0010038922,0.00094405265,0.0004895488,0.00064858893,0.0009317159,0.0005901581],"study_design_candidate":"case_report","study_design_consensus":"case_report","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0001686871,0.00004257458,0.089343555,0.000026350159,0.00002299606,0.90223455,0.0003387368,0.000079294165,0.0055424715,0.00018223374,0.00023533731,0.0017832393],"study_design_scores_gemma":[0.000018057559,0.00014310426,0.11275132,0.000017767432,0.000040419385,0.88430774,0.00031992237,0.00022388763,0.0013124944,0.00010141527,0.00074815034,0.000015678987],"about_ca_topic_score_codex":0.0050410572,"about_ca_topic_score_gemma":0.008003891,"teacher_disagreement_score":0.0050410572,"about_ca_system_score_codex":0.00045143388,"about_ca_system_score_gemma":0.0005234054,"threshold_uncertainty_score":0.014848053},"labels":[],"label_agreement":null},{"id":"W2320477478","doi":"10.1212/nxg.0000000000000058","title":"Reversible white matter lesions associated with mutant <i>EHMT1</i> and Kleefstra syndrome","year":2016,"lang":"en","type":"article","venue":"Neurology Genetics","topic":"Epigenetics and DNA Methylation","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":"Women and Children’s Health Research Institute","funders":"","keywords":"Haploinsufficiency; Histone methyltransferase; Hypotonia; Genetics; Biology; Histone; Gene; Phenotype","score_opus":0.008481746976087941,"score_gpt":0.21113618505579893,"score_spread":0.20265443807971098,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2320477478","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9766308,0.001924741,0.0033925038,0.0006480393,0.00014754152,0.00014263943,0.00045889913,0.00045875035,0.016196107],"genre_scores_gemma":[0.99582833,0.0007032071,0.0011859797,0.00023007192,0.00012230592,0.000017951155,0.00017153152,0.00004091792,0.0016997776],"study_design_codex":"case_report","study_design_gemma":"case_report","domain_scores_codex":[0.99980944,0.000020204743,0.000020382564,0.00005979022,0.000050147148,0.00004004414],"domain_scores_gemma":[0.99960107,0.00005764648,0.00020007418,0.000026693098,0.000031962452,0.00008263843],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00019152551,0.0013533211,0.0004220872,0.00091665564,0.00039770833,0.00040765727,0.0005712248,0.0011478099,0.0042317645],"category_scores_gemma":[0.0005332337,0.0003012128,0.00027725537,0.00042422977,0.0010463224,0.00035750636,0.0004509756,0.0007988239,0.0010794459],"study_design_candidate":"case_report","study_design_consensus":"case_report","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0008618415,0.00021761502,0.019503739,0.00031729665,0.00022191176,0.7283355,0.00031229682,0.00039381324,0.23459575,0.0019550903,0.0016631793,0.011621968],"study_design_scores_gemma":[0.00010851598,0.00052923773,0.085547775,0.000051239913,0.0001944832,0.8744763,0.00013034417,0.00068320666,0.033248737,0.0013827634,0.0036073967,0.000039947645],"about_ca_topic_score_codex":0.0017574406,"about_ca_topic_score_gemma":0.0013921426,"teacher_disagreement_score":0.0042317645,"about_ca_system_score_codex":0.00034525024,"about_ca_system_score_gemma":0.00031388985,"threshold_uncertainty_score":0.01415664},"labels":[],"label_agreement":null},{"id":"W2335001489","doi":"10.1212/nxg.0000000000000063","title":"De novo <i>FUS</i> P525L mutation in Juvenile amyotrophic lateral sclerosis with dysphonia and diplopia","year":2016,"lang":"en","type":"article","venue":"Neurology Genetics","topic":"Amyotrophic Lateral Sclerosis Research","field":"Medicine","cited_by":31,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Montreal Neurological Institute and Hospital","funders":"Canadian Institutes of Health Research; ALS Society of Canada; McGill University; ALS Association; Michael J. Fox Foundation for Parkinson's Research","keywords":"Amyotrophic lateral sclerosis; Diplopia; Medicine; Spasticity; Spastic; Dysarthria; Dyskinesia; Physical medicine and rehabilitation; Pathology; Audiology; Disease; Cerebral palsy; Surgery","score_opus":0.018322162231551385,"score_gpt":0.25050729761116564,"score_spread":0.23218513537961424,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2335001489","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99096936,0.00076445594,0.0013499665,0.0009097873,0.00017647851,0.000068228124,0.00020085937,0.00012793408,0.0054329354],"genre_scores_gemma":[0.9983785,0.0001606948,0.00043339835,0.00025280696,0.00012552648,0.000006711132,0.000049199978,0.000011630262,0.0005815622],"study_design_codex":"case_report","study_design_gemma":"case_report","domain_scores_codex":[0.9996691,0.000039163202,0.00005975242,0.000079386344,0.00006501497,0.00008763542],"domain_scores_gemma":[0.99944574,0.00016735072,0.00014482901,0.0000270035,0.00004167823,0.00017326625],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00023434956,0.0011028107,0.00050294714,0.0009364728,0.0010229036,0.00059249473,0.00049288775,0.0020026509,0.0017093437],"category_scores_gemma":[0.0010600287,0.00037269702,0.00040310307,0.00048698875,0.0008402046,0.00043195506,0.00060606416,0.00071807014,0.00080980104],"study_design_candidate":"case_report","study_design_consensus":"case_report","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.000054338172,0.000028747785,0.006697952,0.000021491172,0.000006522748,0.9840566,0.00015174822,0.000052964293,0.007344884,0.000095956726,0.00030374326,0.001185113],"study_design_scores_gemma":[0.000028044438,0.00012979854,0.026778959,0.000018026698,0.000027487484,0.9689651,0.00012231331,0.0003626181,0.0024498347,0.00014035251,0.0009568266,0.000020683527],"about_ca_topic_score_codex":0.0027767865,"about_ca_topic_score_gemma":0.0034916291,"teacher_disagreement_score":0.0027767865,"about_ca_system_score_codex":0.00058734306,"about_ca_system_score_gemma":0.00035196418,"threshold_uncertainty_score":0.005718291},"labels":[],"label_agreement":null},{"id":"W2341818933","doi":"10.1212/nxg.0000000000000069","title":"Clinical and genetic features of cervical dystonia in a large multicenter cohort","year":2016,"lang":"en","type":"article","venue":"Neurology Genetics","topic":"Botulinum Toxin and Related Neurological Disorders","field":"Medicine","cited_by":53,"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":"Dystonia Coalition; National Institute of Neurological Disorders and Stroke; Parkinsonfonden; Health Science Center, University of Tennessee; St. Jude Medical; National Institutes of Health; University of Toronto; Omeros Corporation; Spastic Paraplegia Foundation; Adamas Pharmaceuticals; Ipsen; Prothena; Psyadon Pharmaceuticals; ACADIA Pharmaceuticals; Parkinson Study Group; Merz Pharmaceuticals; Ultragenyx Pharmaceutical; Medical University of South Carolina; University of Louisville; University of Missouri; Pfizer; National Parkinson Foundation; University of Rochester; UCB Pharma; Michael J. Fox Foundation for Parkinson's Research; Emory University; CHDI Foundation; Medtronic; American Parkinson Disease Association; Dystonia Medical Research Foundation; Parkinson's Disease Foundation; National Center for Advancing Translational Sciences; Teva Pharmaceutical Industries; University of South Carolina; US WorldMeds; Mayo Clinic; University of Michigan; Acorda Therapeutics; Dana Foundation; Ipsen Biopharmaceuticals; Alberta Innovates; Neurocrine Biosciences; Benign Essential Blepharospasm Research Foundation; Allergan; International Parkinson and Movement Disorder Society; H. Lundbeck A/S; American Academy of Neurology","keywords":"Cervical dystonia; Dystonia; Medicine; Missense mutation; Cohort; Internal medicine; Pediatrics; Genetics; Biology; Mutation; Psychiatry; Gene","score_opus":0.013753262617699446,"score_gpt":0.2972990635314182,"score_spread":0.2835458009137188,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2341818933","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99887246,0.00011676986,0.000055127097,0.000043094034,0.0000043728664,0.000026024309,0.0004933744,0.0000038159124,0.0003849499],"genre_scores_gemma":[0.998517,0.00010760646,0.00016746746,0.00006915567,0.000014512068,0.000051413946,0.0008004083,0.0000046763466,0.00026781036],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99952614,0.00008755906,0.00003794113,0.00020843833,0.00007600294,0.00006392575],"domain_scores_gemma":[0.9995034,0.000055671913,0.00016990224,0.000065711254,0.00007657641,0.00012872794],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00056396687,0.00050832145,0.00040402406,0.00075348635,0.0011659719,0.00069801643,0.0005838625,0.0007236331,0.0026345155],"category_scores_gemma":[0.0019165702,0.0003024637,0.00035413474,0.0006744418,0.00029517993,0.0004339377,0.0007044338,0.00038960608,0.0004550005],"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":[0.00024280275,0.00006339587,0.9956049,0.000010500162,0.00006308269,0.0006357954,0.0001923582,0.000023753395,0.0012033721,0.000023056527,0.00041816963,0.0015188885],"study_design_scores_gemma":[0.000040863062,0.00015830148,0.99582577,0.00001447021,0.00004476273,0.0026918608,0.0004394593,0.00013371946,0.000070276015,0.00002862111,0.00054509763,0.0000068106147],"about_ca_topic_score_codex":0.010227612,"about_ca_topic_score_gemma":0.013484144,"teacher_disagreement_score":0.010227612,"about_ca_system_score_codex":0.00039588095,"about_ca_system_score_gemma":0.0003883044,"threshold_uncertainty_score":0.020336151},"labels":[],"label_agreement":null},{"id":"W2510648196","doi":"10.1212/nxg.0000000000000104","title":"<i>GBA</i> p.T369M substitution in Parkinson disease: Polymorphism or association? A meta-analysis","year":2016,"lang":"en","type":"article","venue":"Neurology Genetics","topic":"Lysosomal Storage Disorders Research","field":"Medicine","cited_by":100,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Université du Québec à Trois-Rivières","funders":"National Human Genome Research Institute; Canadian Institutes of Health Research; National Institutes of Health; ALS Society of Canada; McGill University; Parkinson's Disease Foundation; ALS Association; Sanofi; Brookdale Foundation; Michael J. Fox Foundation for Parkinson's Research","keywords":"Glucocerebrosidase; Internal medicine; Disease; Gastroenterology; Medicine; Parkinson's disease","score_opus":0.05927248447211916,"score_gpt":0.3191264790258864,"score_spread":0.2598539945537673,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2510648196","genre_codex":"review","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":null,"domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.14546116,0.8459386,0.0015909605,0.0012365181,0.0006708925,0.00011063989,0.0036716396,0.00007487805,0.0012447796],"genre_scores_gemma":[0.89253396,0.100867294,0.0010803486,0.0014144337,0.00059857994,0.00024589206,0.002538805,0.000060520713,0.00066017214],"study_design_codex":"meta_analysis","study_design_gemma":"meta_analysis","domain_scores_codex":[0.9968983,0.0010703119,0.00068045105,0.00087250903,0.00025543428,0.00022298271],"domain_scores_gemma":[0.99513406,0.00331689,0.00067630905,0.0003347845,0.0003801609,0.00015771596],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0042679952,0.0012950093,0.0074094115,0.0017505651,0.0006972207,0.0020933095,0.0013363716,0.0022835536,0.004429726],"category_scores_gemma":[0.0067274454,0.0007327323,0.016432678,0.0050423727,0.00050992897,0.00089368236,0.0008077672,0.0016821136,0.00032816976],"study_design_candidate":"meta_analysis","study_design_consensus":"meta_analysis","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.011487239,0.00007247588,0.1915144,0.0391454,0.7314904,0.00077800255,0.00017929333,0.0008211908,0.0013538295,0.00036036433,0.003388821,0.019408625],"study_design_scores_gemma":[0.0011644108,0.00038052408,0.1114585,0.003172571,0.87829006,0.0004598427,0.00013149169,0.00075663987,0.00019319273,0.0005822357,0.0033601285,0.00005045567],"about_ca_topic_score_codex":0.005904835,"about_ca_topic_score_gemma":0.0066658617,"teacher_disagreement_score":0.0074094115,"about_ca_system_score_codex":0.0006301311,"about_ca_system_score_gemma":0.0006033838,"threshold_uncertainty_score":0.022571564},"labels":[],"label_agreement":null},{"id":"W2559826491","doi":"10.1212/nxg.0000000000000122","title":"Clinical and genetic study of hereditary spastic paraplegia in Canada","year":2016,"lang":"en","type":"article","venue":"Neurology Genetics","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":98,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":true,"ca_institutions":"Université du Québec à Montréal","funders":"Strong","keywords":"Hereditary spastic paraplegia; Medicine; Odds ratio; Internal medicine; Pediatrics; Confidence interval; Observational study; Cohort; Spastic; Physical therapy; Genetics; Phenotype; Gene; Biology","score_opus":0.043603351396241274,"score_gpt":0.28213279521369683,"score_spread":0.23852944381745556,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2559826491","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.98862565,0.0007464487,0.00016404723,0.00051393826,0.00001714085,0.00012687253,0.0064103818,0.000015525764,0.0033799866],"genre_scores_gemma":[0.9971403,0.00036077757,0.00021505059,0.00017546359,0.0000067972173,0.00002782745,0.001408457,0.0000044532962,0.00066086696],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99925786,0.00004946618,0.00005427629,0.00014064644,0.00026790073,0.00022978727],"domain_scores_gemma":[0.9978909,0.00008152908,0.0003605758,0.000046078476,0.0011054416,0.00051551167],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0004163736,0.00040504386,0.00035338686,0.0014170159,0.003221769,0.0006609814,0.0009271729,0.000491108,0.002380496],"category_scores_gemma":[0.0016571553,0.00027078518,0.00038247198,0.004875855,0.0008003497,0.00022210929,0.0008429527,0.00058991485,0.00021774966],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":true,"about_ca_topic_consensus":true,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00006737431,0.000041961404,0.994372,0.000035166453,0.000037588714,0.0003625787,0.0004143439,0.000108492226,0.0003695491,0.00014171933,0.0013654188,0.0026838132],"study_design_scores_gemma":[0.00001524697,0.000028959452,0.9975822,0.00003369468,0.000017051305,0.00043585018,0.00057861535,0.00024397246,0.00008231806,0.000040110932,0.0009325826,0.00000929976],"about_ca_topic_score_codex":0.99111813,"about_ca_topic_score_gemma":0.99249214,"teacher_disagreement_score":0.023426823,"about_ca_system_score_codex":0.023426823,"about_ca_system_score_gemma":0.03761336,"threshold_uncertainty_score":0.16997427},"labels":[],"label_agreement":null},{"id":"W2559857749","doi":"10.1212/nxg.0000000000000115","title":"FHF1 (FGF12) epileptic encephalopathy","year":2016,"lang":"en","type":"article","venue":"Neurology Genetics","topic":"Genetics and Neurodevelopmental Disorders","field":"Biochemistry, Genetics and Molecular Biology","cited_by":41,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":true,"ca_institutions":"Université de Montréal; Hôpital Notre-Dame; Centre Hospitalier Universitaire Sainte-Justine","funders":"University of Toronto; Genome Canada; National Institute for Health and Care Research; National Institute of Neurological Disorders and Stroke; Ontario Brain Institute; Wellcome Trust; McGill University","keywords":"Medicine; Epilepsy; Sanger sequencing; Mutation; Bioinformatics; Psychiatry; Genetics; Gene; Biology","score_opus":0.007389236391675741,"score_gpt":0.2144486902610636,"score_spread":0.20705945386938787,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2559857749","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.8974937,0.006097653,0.0061313813,0.0065409536,0.0007308323,0.00036578203,0.0028213458,0.00067113125,0.07914728],"genre_scores_gemma":[0.97715604,0.0011653414,0.0013450548,0.0011042925,0.00028791866,0.000056096218,0.0007243736,0.00003336268,0.018127615],"study_design_codex":"case_report","study_design_gemma":"case_report","domain_scores_codex":[0.99986815,0.000014676062,0.000010705275,0.00003158939,0.000024270252,0.000050467857],"domain_scores_gemma":[0.9997799,0.00006166629,0.000038267524,0.000016800555,0.00003100595,0.000072415685],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0001340781,0.0008953256,0.0003420897,0.0005808679,0.00088224316,0.00020797271,0.0003741951,0.0009527112,0.0076664253],"category_scores_gemma":[0.0010017557,0.000105666,0.00026994536,0.00044476942,0.0004332105,0.0003636731,0.000374431,0.00057960703,0.0013781269],"study_design_candidate":"case_report","study_design_consensus":"case_report","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00028907822,0.000070121234,0.017926803,0.00010006924,0.000029175959,0.95041585,0.00015911246,0.00014680286,0.004575334,0.0012417675,0.0036882856,0.021357588],"study_design_scores_gemma":[0.000047994545,0.00024573097,0.040269125,0.00007667224,0.000046446625,0.9362635,0.00015808977,0.00038109574,0.0040980997,0.0010868828,0.017303826,0.000022528078],"about_ca_topic_score_codex":0.007174796,"about_ca_topic_score_gemma":0.0044404487,"teacher_disagreement_score":0.0076664253,"about_ca_system_score_codex":0.00057331217,"about_ca_system_score_gemma":0.00051778724,"threshold_uncertainty_score":0.025646806},"labels":[],"label_agreement":null},{"id":"W2619159900","doi":"10.1212/nxg.0000000000000156","title":"Febrile ataxia and myokymia broaden the SPG26 hereditary spastic paraplegia phenotype","year":2017,"lang":"en","type":"article","venue":"Neurology Genetics","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":10,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Toronto","funders":"Higher Education Commision, Pakistan; National University of Sciences and Technology; Hospital for Sick Children; University of Toronto; Johns Hopkins University","keywords":"Myokymia; Hereditary spastic paraplegia; Phenotype; Ataxia; Genetics; Medicine; Biology; Physical medicine and rehabilitation; Psychiatry; Gene","score_opus":0.04166302485557018,"score_gpt":0.27315431508335086,"score_spread":0.2314912902277807,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2619159900","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.94567657,0.015896963,0.0045326347,0.0010362443,0.0001962292,0.000093331124,0.0006624142,0.00030351846,0.03160198],"genre_scores_gemma":[0.9876208,0.0050931694,0.0023055696,0.0004340283,0.0001917873,0.000014355241,0.00025938873,0.000028155237,0.0040527307],"study_design_codex":"case_report","study_design_gemma":"case_report","domain_scores_codex":[0.99986184,0.000021943317,0.000017627093,0.0000259412,0.000040673887,0.000031938118],"domain_scores_gemma":[0.99984837,0.000030156929,0.00005439223,0.000011169159,0.000017892386,0.00003810528],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00013476139,0.00097525795,0.0005157489,0.000770935,0.00033775443,0.00026464276,0.00023624886,0.00070474605,0.0031132898],"category_scores_gemma":[0.00046376896,0.00016373552,0.00024735948,0.0005745315,0.00048143746,0.0003212503,0.0006091926,0.0003786628,0.0012072817],"study_design_candidate":"case_report","study_design_consensus":"case_report","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0003066306,0.000081400955,0.04129406,0.00041103148,0.000060238635,0.8459907,0.0005464884,0.00032141845,0.042512026,0.0022358296,0.004423997,0.06181623],"study_design_scores_gemma":[0.000020263295,0.00009871281,0.055064872,0.000115120616,0.000033618635,0.93023264,0.00012948383,0.00010139786,0.002600652,0.0009966784,0.01058991,0.000016721244],"about_ca_topic_score_codex":0.00078835565,"about_ca_topic_score_gemma":0.0013971565,"teacher_disagreement_score":0.0031132898,"about_ca_system_score_codex":0.0001839136,"about_ca_system_score_gemma":0.00020652858,"threshold_uncertainty_score":0.010415018},"labels":[],"label_agreement":null},{"id":"W2619882435","doi":"10.1212/nxg.0000000000000148","title":"<i>ARHGEF9</i> disease","year":2017,"lang":"en","type":"article","venue":"Neurology Genetics","topic":"Congenital Ear and Nasal Anomalies","field":"Medicine","cited_by":42,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Toronto","funders":"National Institute of Neurological Disorders and Stroke; Science and Engineering Research Board; Ontario Genomics; Indian Council of Medical Research; University of Mysore; National Institutes of Health; Hospital for Sick Children; Autism Speaks; University of Toronto; Canadian Institutes of Health Research; Genome Canada; Ontario Genomics Institute; Government of Ontario","keywords":"Intellectual disability; Epilepsy; Loss function; Phenotype; Exon; Mutation; Facial dysmorphism; Genetics; Disease; Medicine; Genetic testing; Pediatrics; Gene; Biology; Psychiatry; Pathology","score_opus":0.02457271083163875,"score_gpt":0.28944409061207527,"score_spread":0.2648713797804365,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2619882435","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.92608494,0.014657395,0.0040230956,0.0012733194,0.000307239,0.00024803646,0.007165438,0.0004658241,0.04577472],"genre_scores_gemma":[0.9864847,0.0018670425,0.0034881628,0.0005097961,0.00025431227,0.00004393525,0.0017761524,0.00005451476,0.0055213203],"study_design_codex":"observational","study_design_gemma":"case_report","domain_scores_codex":[0.9998474,0.000015123273,0.000021776204,0.00006193196,0.000025123873,0.00002852566],"domain_scores_gemma":[0.9998221,0.000043720323,0.00007073192,0.000008480261,0.000022307468,0.00003281084],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00016148959,0.0008232339,0.00027631962,0.0008608764,0.000330148,0.000321118,0.00039804875,0.0004819517,0.008877844],"category_scores_gemma":[0.0004011771,0.000083832325,0.00016842599,0.00048758514,0.000305174,0.0002178452,0.00020338062,0.00020385142,0.0016795021],"study_design_candidate":"case_report","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":[0.0011901351,0.00024609154,0.358323,0.0014822535,0.0002676493,0.25323877,0.0008863576,0.0004939104,0.17109258,0.0028924989,0.031316668,0.17857017],"study_design_scores_gemma":[0.00012113662,0.00029284536,0.19015817,0.0003315703,0.00020934404,0.7289131,0.00026284336,0.0003479247,0.026309503,0.00069626136,0.052328605,0.000028643248],"about_ca_topic_score_codex":0.0004264141,"about_ca_topic_score_gemma":0.0006202512,"teacher_disagreement_score":0.008877844,"about_ca_system_score_codex":0.00019186767,"about_ca_system_score_gemma":0.0002012151,"threshold_uncertainty_score":0.029699326},"labels":[],"label_agreement":null},{"id":"W2745723691","doi":"10.1212/nxg.0000000000000178","title":"Ultra-rare mutations in <i>SRCAP</i> segregate in Caribbean Hispanic families with Alzheimer disease","year":2017,"lang":"en","type":"article","venue":"Neurology Genetics","topic":"Congenital limb and hand anomalies","field":"Biochemistry, Genetics and Molecular Biology","cited_by":11,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Discovery Centre; University of Toronto","funders":"National Institutes of Health; Eisai; W. Garfield Weston Foundation; National Center for Advancing Translational Sciences; Wellcome Trust; Medical Research Council; Biogen; Celgene; Teva Pharmaceutical Industries; BrightFocus Foundation; Pfizer; National Institute on Aging; Alzheimer's Association; U.S. Department of Defense; Sanofi; National Multiple Sclerosis Society","keywords":"Missense mutation; Biology; Exome sequencing; Exome; Genetics; Mutation; Gene","score_opus":0.012429079670756103,"score_gpt":0.23994301766935916,"score_spread":0.22751393799860306,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2745723691","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99947697,0.000078352634,0.00007359046,0.00001416808,0.0000011347296,0.000001979485,0.00006367388,0.0000039591832,0.00028617238],"genre_scores_gemma":[0.99949944,0.000078160054,0.0001452332,0.000012760859,0.0000030617707,0.0000041132007,0.000077782606,0.000005364681,0.00017395538],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99991727,0.000011297565,0.000006113679,0.000026132251,0.000017887938,0.000021290802],"domain_scores_gemma":[0.9997987,0.000039508173,0.00010229147,0.0000094193765,0.000019816458,0.000030375224],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00009888806,0.00046896216,0.00017463473,0.00085046963,0.00039820853,0.00032115844,0.00017699372,0.0002896697,0.0031336276],"category_scores_gemma":[0.00059678877,0.00017793251,0.00011858493,0.000458245,0.00024234512,0.00010684752,0.00024692545,0.00017364678,0.00020291303],"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":[0.00071055524,0.00005507942,0.9024747,0.000049127742,0.000092342336,0.0068426165,0.00094559626,0.00014471982,0.07947711,0.00022276085,0.00026009773,0.008725313],"study_design_scores_gemma":[0.0000198042,0.00010726928,0.9826581,0.000033034914,0.00008776356,0.010768734,0.0009389817,0.00047471828,0.0041259956,0.00013503483,0.0006402249,0.000010490374],"about_ca_topic_score_codex":0.008060863,"about_ca_topic_score_gemma":0.0106146615,"teacher_disagreement_score":0.008060863,"about_ca_system_score_codex":0.00018148955,"about_ca_system_score_gemma":0.00016009882,"threshold_uncertainty_score":0.016027927},"labels":[],"label_agreement":null},{"id":"W2761271661","doi":"10.1212/nxg.0000000000000194","title":"The Alzheimer's Disease Sequencing Project: Study design and sample selection","year":2017,"lang":"en","type":"article","venue":"Neurology Genetics","topic":"Alzheimer's disease research and treatments","field":"Medicine","cited_by":237,"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":"Mailman School of Public Health, Columbia University; National Heart, Lung, and Blood Institute; National Institute on Aging; Perelman School of Medicine, University of Pennsylvania; University of California, San Diego; University College London; American Society for Bone and Mineral Research; Edward N. and Della L. Thome Memorial Foundation; National Institute of Neurological Disorders and Stroke; University of Pittsburgh; School of Medicine, Indiana University; Denali Therapeutics; Massachusetts Institute of Technology; School of Medicine, Boston University; Rainwater Charitable Foundation; University of Florida; Case Western Reserve University; Cleveland Clinic; Harvard University; JPB Foundation; University of Chicago; Fidelity Foundation; University of Texas at Austin; National Institutes of Health; San Diego State University; CurePSP; University of Pennsylvania; University of Miami; McKnight Foundation; Alzheimer's Association; Michael J. Fox Foundation for Parkinson's Research; Broad Institute; U.S. Department of Defense","keywords":"Disease; Dementia; Epidemiology; Alzheimer's disease; Gerontology; Medicine; Genetics; Biology; Pathology","score_opus":0.10079678271556884,"score_gpt":0.36789650359356824,"score_spread":0.2670997208779994,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2761271661","genre_codex":"protocol","genre_gemma":"methods","domain_codex":null,"domain_gemma":"methods","model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"methods","genre_consensus":null,"domain_candidate":"methods","domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.30928338,0.008410483,0.110045224,0.004103336,0.0015280474,0.43081635,0.1189898,0.0008062363,0.016017215],"genre_scores_gemma":[0.24140756,0.0031792803,0.080347195,0.0050857547,0.00097269466,0.61010534,0.04876646,0.00034463566,0.009791131],"study_design_codex":"observational","study_design_gemma":"not_applicable","domain_scores_codex":[0.99101686,0.0052454188,0.00087528175,0.0014083098,0.0010957698,0.0003583627],"domain_scores_gemma":[0.9951355,0.0012546052,0.00051965925,0.00088660175,0.001548978,0.0006546347],"candidate_categories":["metaresearch"],"consensus_categories":[],"category_scores_codex":[0.016953325,0.0021616563,0.002715502,0.0019732032,0.0014809389,0.0012700417,0.0024652716,0.0015436125,0.0089874165],"category_scores_gemma":[0.018323602,0.0015779968,0.00072038,0.0029382915,0.00087505195,0.0007134873,0.0017938074,0.0011873613,0.003402614],"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":[0.072868,0.007964128,0.33972034,0.0068364977,0.0034600962,0.005357211,0.004453221,0.007948333,0.009346509,0.01104465,0.27487245,0.25612864],"study_design_scores_gemma":[0.047119398,0.02467804,0.4799296,0.0025515386,0.0050741103,0.0041098413,0.0016249352,0.023243038,0.0032815863,0.019650452,0.3881802,0.00055721164],"about_ca_topic_score_codex":0.009616253,"about_ca_topic_score_gemma":0.013031041,"teacher_disagreement_score":0.98304665,"about_ca_system_score_codex":0.0011572939,"about_ca_system_score_gemma":0.0041342704,"threshold_uncertainty_score":0.0896588},"labels":[],"label_agreement":null},{"id":"W2766106979","doi":"10.1212/nxg.0000000000000195","title":"No rare deleterious variants from <i>STK32B</i> , <i>PPARGC1A</i> , and <i>CTNNA3</i> are associated with essential tremor","year":2017,"lang":"en","type":"article","venue":"Neurology Genetics","topic":"Neurological disorders and treatments","field":"Medicine","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":"Xenon Pharmaceuticals (Canada); Université Laval; University of Saskatchewan; University of British Columbia; Saskatchewan Health Authority; Montreal Neurological Institute and Hospital","funders":"Canadian Institutes of Health Research","keywords":"Biology; Genetics; Medicine","score_opus":0.014427540418685502,"score_gpt":0.2407868951411834,"score_spread":0.2263593547224979,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2766106979","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9977526,0.00034665383,0.00066666637,0.00007879085,0.000011518209,0.000009841613,0.00040184736,0.000024770594,0.000707257],"genre_scores_gemma":[0.9990953,0.000056192726,0.00036646784,0.00003853692,0.000009642383,0.000004006684,0.00027463055,0.000008807063,0.0001463974],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99960524,0.00005009313,0.00005754873,0.00014900634,0.00009833168,0.000039836235],"domain_scores_gemma":[0.9990609,0.0002597438,0.00040303558,0.00010534729,0.000059527916,0.00011135808],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00037813594,0.00036719168,0.0003710031,0.00040941895,0.0003747754,0.00042425323,0.00029510228,0.0005208116,0.002860092],"category_scores_gemma":[0.0013749466,0.00015989578,0.0004649112,0.00043198635,0.00046691686,0.00015244399,0.00027472066,0.00032389874,0.0003189797],"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":[0.004271992,0.00018573248,0.7977727,0.00017996092,0.0011498606,0.007978762,0.00033127735,0.0007204017,0.16549672,0.000561088,0.0009094849,0.020442063],"study_design_scores_gemma":[0.00021740107,0.00044030018,0.9668909,0.000057318837,0.00074787205,0.014054002,0.000111718895,0.0011650117,0.013689665,0.0006841596,0.001920001,0.000021636968],"about_ca_topic_score_codex":0.0012572933,"about_ca_topic_score_gemma":0.0031210585,"teacher_disagreement_score":0.002860092,"about_ca_system_score_codex":0.00015220811,"about_ca_system_score_gemma":0.00023541645,"threshold_uncertainty_score":0.009567976},"labels":[],"label_agreement":null},{"id":"W2775797405","doi":"10.1212/nxg.0000000000000200","title":"<i>CDKL5</i> variants","year":2017,"lang":"he","type":"article","venue":"Neurology Genetics","topic":"Genetics and Neurodevelopmental Disorders","field":"Biochemistry, Genetics and Molecular Biology","cited_by":85,"is_retracted":false,"has_abstract":true,"route_ca_aff":false,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"","funders":"National Institutes of Health; University of Colorado School of Medicine, Anschutz Medical Campus; International Foundation for CDKL5 Research; Max-Planck-Gesellschaft; Bundesministerium für Bildung und Forschung; Eunice Kennedy Shriver National Institute of Child Health and Human Development; Economic and Social Research Council; Curtin University of Technology; Rosetrees Trust; Children's Hospital Colorado; Mallinckrodt Pharmaceuticals; Actelion Pharmaceuticals; National Health and Medical Research Council; LouLou Foundation; Rett Syndrome Association of Australia; Edimer Pharmaceuticals; Questcor Pharmaceuticals; Citizens United for Research in Epilepsy; University of Pennsylvania; Rett Syndrome Research Trust; AveXis; Biogen","keywords":"Missense mutation; Biology; Nonsense; Exon; Genetics; RNA splicing; Population; Alternative splicing; Allele; Gene; Computational biology; Bioinformatics; Mutation; Medicine","score_opus":0.013716332022619904,"score_gpt":0.25061549751316337,"score_spread":0.23689916549054346,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2775797405","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9473198,0.0011781378,0.039827753,0.0007632182,0.00007414523,0.00015171366,0.005102067,0.00058466144,0.0049984097],"genre_scores_gemma":[0.9835137,0.00022908715,0.013509552,0.0002529496,0.000045710152,0.000023818555,0.0020662893,0.000047982656,0.0003108483],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99952507,0.00006619308,0.00006905458,0.00019781064,0.00009237536,0.000049530965],"domain_scores_gemma":[0.9991247,0.00037458382,0.00027348602,0.000102007296,0.00007122011,0.000054011103],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0009109235,0.0004940232,0.00026786767,0.00072660664,0.00035472098,0.0008412969,0.000550534,0.0004941751,0.0027077133],"category_scores_gemma":[0.0026807906,0.00012224836,0.0007242993,0.0005470484,0.00042942088,0.00036659685,0.00037250732,0.0005622183,0.00041441707],"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":[0.00088135805,0.000094521514,0.86971587,0.00022962037,0.00061824574,0.002851359,0.00025942686,0.011859132,0.03650826,0.003162563,0.0035522962,0.070267394],"study_design_scores_gemma":[0.00026680043,0.00035201744,0.83073634,0.00020631174,0.0009151843,0.013074052,0.00055633514,0.060978837,0.06511407,0.01219973,0.015482658,0.00011759506],"about_ca_topic_score_codex":0.0052188183,"about_ca_topic_score_gemma":0.0077800094,"teacher_disagreement_score":0.0052188183,"about_ca_system_score_codex":0.00057785184,"about_ca_system_score_gemma":0.0005821607,"threshold_uncertainty_score":0.010376871},"labels":[],"label_agreement":null},{"id":"W2785697019","doi":"10.1212/nxg.0000000000000216","title":"<i>CYP2C19</i> variant mitigates Alzheimer disease pathophysiology in vivo and postmortem","year":2018,"lang":"en","type":"article","venue":"Neurology Genetics","topic":"Alzheimer's disease research and treatments","field":"Medicine","cited_by":13,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"McGill University; Douglas Mental Health University Institute; Montreal Neurological Institute and Hospital; HEC Montréal","funders":"National Institute on Aging; National Institute of Biomedical Imaging and Bioengineering; Canadian Institutes of Health Research; Genentech; National Institutes of Health; IXICO; H. Lundbeck A/S; Servier; Eisai; Coordenação de Aperfeiçoamento de Pessoal de Nível Superior; Alzheimer's Drug Discovery Foundation; Weston Brain Institute; Northern California Institute for Research and Education; Pfizer; BioClinica; Biogen; University of Southern California; Illinois Department of Public Health; Novartis Pharmaceuticals Corporation; U.S. Department of Defense; Eli Lilly and Company; Consortium canadien en neurodégénérescence associée au vieillissement; Bristol-Myers Squibb; F. Hoffmann-La Roche; Alzheimer's Association; Foundation for the National Institutes of Health; Alzheimer's Disease Neuroimaging Initiative; Meso Scale Diagnostics","keywords":"Postmortem studies; Posterior cingulate; Alzheimer's Disease Neuroimaging Initiative; Neuroimaging; Alzheimer's disease; Internal medicine; Pathology; In vivo; Allele; Medicine; Oncology; Disease; Psychology; Neuroscience; Biology; Cognition; Genetics; Gene","score_opus":0.018985837491291395,"score_gpt":0.290122847452412,"score_spread":0.2711370099611206,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2785697019","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99776113,0.0001897264,0.00096047804,0.0001245518,0.000012935742,0.000015165964,0.00040906479,0.000052313768,0.00047457957],"genre_scores_gemma":[0.9985884,0.0000682638,0.0006229818,0.000096164345,0.000017329277,0.000013081574,0.00027201948,0.000021641197,0.00030007184],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9997931,0.00005505974,0.000012441763,0.00007997656,0.00003172722,0.000027827738],"domain_scores_gemma":[0.9995695,0.000055968285,0.0001891165,0.000093303475,0.00003713572,0.00005490937],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0004379978,0.0003223855,0.00035380572,0.00023253002,0.00021957411,0.00043230437,0.00019271825,0.00034180234,0.0015082231],"category_scores_gemma":[0.0006404754,0.0001922834,0.00036300614,0.00018466497,0.0003245008,0.00018231949,0.00013557934,0.00042501668,0.00021113013],"study_design_candidate":"bench_or_experimental","study_design_consensus":"bench_or_experimental","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.012645259,0.0006862223,0.19338802,0.00011539003,0.0013629263,0.00093127834,0.00018518789,0.00057716755,0.7684275,0.0004172211,0.0017727865,0.019491058],"study_design_scores_gemma":[0.00039327724,0.0032842925,0.8935453,0.000012231654,0.00059884007,0.0021316563,0.00011308187,0.0019433798,0.09569671,0.0005206183,0.0017367479,0.000023765584],"about_ca_topic_score_codex":0.0019426072,"about_ca_topic_score_gemma":0.0024055636,"teacher_disagreement_score":0.0019426072,"about_ca_system_score_codex":0.00019373487,"about_ca_system_score_gemma":0.0001795516,"threshold_uncertainty_score":0.005045533},"labels":[],"label_agreement":null},{"id":"W2803317584","doi":"10.1212/nxg.0000000000000239","title":"Determining the incidence of familiality in ALS","year":2018,"lang":"de","type":"article","venue":"Neurology Genetics","topic":"Amyotrophic Lateral Sclerosis Research","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":"Trinity College","funders":"Cilag; Allergan; Science Foundation Ireland; Motor Neurone Disease Association; National Institute of Neurological Disorders and Stroke; Sanofi; Royal College of Surgeons in Ireland; Cytokinetics; Biogen; Health Research Board","keywords":"Endophenotype; Amyotrophic lateral sclerosis; Incidence (geometry); Population; Medicine; Genetic counseling; Confidence interval; Pediatrics; Demography; Disease; Internal medicine; Psychiatry; Biology; Genetics","score_opus":0.0520602576753042,"score_gpt":0.34600019561700773,"score_spread":0.29393993794170353,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2803317584","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9970373,0.00047639525,0.00039119768,0.00010159614,0.000007054403,0.000009982345,0.0009523794,0.000014635933,0.0010095044],"genre_scores_gemma":[0.9985556,0.00021600928,0.00034714132,0.000016177428,0.000006310167,0.0000080103255,0.00067488325,0.000003908097,0.00017190946],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9989048,0.00029659606,0.0001479846,0.00028803165,0.00025389873,0.00010865283],"domain_scores_gemma":[0.99710506,0.00039328093,0.0015635127,0.00023203775,0.0005569557,0.00014907501],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0021465977,0.00012698442,0.00018064238,0.0012670386,0.0002495728,0.00048628508,0.0004722771,0.00030835718,0.001000339],"category_scores_gemma":[0.006809363,0.0001947706,0.0002755517,0.0008257802,0.00029931855,0.000451625,0.00040685263,0.00032475212,0.0002193929],"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":[0.000029451518,0.000004202185,0.99782985,0.0000051757215,0.000020607054,0.000046024186,0.000052995343,0.00008046972,0.00010504652,0.00002365334,0.00010491967,0.0016974796],"study_design_scores_gemma":[0.0000011163374,0.000024352203,0.9990815,0.0000062693784,0.0000063693337,0.00033548544,0.000069231726,0.0002245681,0.00006480558,0.000025530335,0.00015890751,0.0000019719914],"about_ca_topic_score_codex":0.013498112,"about_ca_topic_score_gemma":0.011928305,"teacher_disagreement_score":0.013498112,"about_ca_system_score_codex":0.000632695,"about_ca_system_score_gemma":0.00042929727,"threshold_uncertainty_score":0.026839077},"labels":[],"label_agreement":null},{"id":"W2883002472","doi":"10.1212/nxg.0000000000000263","title":"Novel <i>ELOVL4</i> mutation associated with erythrokeratodermia and spinocerebellar ataxia (SCA 34)","year":2018,"lang":"en","type":"article","venue":"Neurology Genetics","topic":"Connexins and lens biology","field":"Biochemistry, Genetics and Molecular Biology","cited_by":35,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Ottawa Hospital; University of Ottawa","funders":"","keywords":"Hyperkeratosis; Genetics; Dermatology; Loricrin; Palmoplantar keratoderma; Medicine; Biology; Gene","score_opus":0.00917382241964522,"score_gpt":0.22378322474853038,"score_spread":0.21460940232888515,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2883002472","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.96299523,0.0013112035,0.008252273,0.003982061,0.00071100617,0.0003163163,0.001206581,0.0007904443,0.020434836],"genre_scores_gemma":[0.9911289,0.000169775,0.003383322,0.0010887003,0.00041072856,0.00003887043,0.00044629513,0.00008262108,0.0032506618],"study_design_codex":"case_report","study_design_gemma":"case_report","domain_scores_codex":[0.9994604,0.00007487317,0.000062590574,0.00015271315,0.00013054651,0.00011894436],"domain_scores_gemma":[0.9991867,0.00024475905,0.00024031517,0.000032641074,0.00007366766,0.00022195655],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00034142734,0.0021041778,0.0007811133,0.001229208,0.0011807627,0.0006479059,0.0015930375,0.003752448,0.0057275738],"category_scores_gemma":[0.0010709638,0.00035755662,0.0010207099,0.0007762941,0.0015867582,0.0006586934,0.0009903291,0.0018327694,0.0014714797],"study_design_candidate":"case_report","study_design_consensus":"case_report","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0001721481,0.00015905418,0.005533001,0.00007427278,0.00006353954,0.95650256,0.00022135832,0.00033145427,0.029774325,0.0015339655,0.0020723173,0.0035619317],"study_design_scores_gemma":[0.000104828534,0.00024354429,0.023031697,0.000072274015,0.00011598991,0.95940024,0.00014373842,0.0017106947,0.007723652,0.0012742543,0.006103514,0.00007551186],"about_ca_topic_score_codex":0.0026862833,"about_ca_topic_score_gemma":0.0030475222,"teacher_disagreement_score":0.0057275738,"about_ca_system_score_codex":0.0007688279,"about_ca_system_score_gemma":0.00052305404,"threshold_uncertainty_score":0.019160569},"labels":[],"label_agreement":null},{"id":"W2902034093","doi":"10.1212/nxg.0000000000000286","title":"Rare genetic variation implicated in non-Hispanic white families with Alzheimer disease","year":2018,"lang":"en","type":"article","venue":"Neurology Genetics","topic":"Genetic Associations and Epidemiology","field":"Biochemistry, Genetics and Molecular Biology","cited_by":28,"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":"U.S. National Library of Medicine; National Institute of Neurological Disorders and Stroke; National Institute of Diabetes and Digestive and Kidney Diseases; National Heart, Lung, and Blood Institute; National Institute on Aging; Medizinische Universität Graz; Karl-Franzens-Universität Graz; National Institutes of Health; Österreichische Forschungsförderungsgesellschaft; Oesterreichische Nationalbank; University of California, San Diego; University of Toronto; Nederlandse Organisatie voor Wetenschappelijk Onderzoek; Erasmus Medisch Centrum; National Institute on Deafness and Other Communication Disorders; Capital Medical University; Austrian Science Fund; National Human Genome Research Institute; Russian Foundation for Basic Research; ZonMw; Institut National de la Santé et de la Recherche Médicale; Vanderbilt University; EU Joint Programme – Neurodegenerative Disease Research; Fondation Leducq; Agence Nationale de la Recherche; Wellcome Trust; University College London; Case Western Reserve University; Cleveland Clinic; CurePSP; University of Pennsylvania; European Commission; Denali Therapeutics; Fidelity Foundation; Biogen; Pfizer; University of Miami; Deutsches Zentrum für Neurodegenerative Erkrankungen; McKnight Foundation; Alzheimer's Association; U.S. Department of Defense; Cystic Fibrosis Foundation; Edward N. and Della L. Thome Memorial Foundation; U.S. Department of Agriculture; U.S. Department of Health and Human Services","keywords":"Genetics; Disease; Gene; Candidate gene; Genetic variation; Biology; Medicine; Pathology","score_opus":0.009914374619999148,"score_gpt":0.24601378058293316,"score_spread":0.23609940596293402,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2902034093","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9984742,0.00017578162,0.00050135085,0.00002445032,0.0000045458078,0.000008741208,0.00027994753,0.000016562386,0.00051444286],"genre_scores_gemma":[0.9984523,0.00012312518,0.0007014585,0.000028697448,0.000011611018,0.000011717852,0.0003752612,0.000010469452,0.00028525235],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99957246,0.000082138395,0.000034090626,0.00017796681,0.00009047623,0.000042857286],"domain_scores_gemma":[0.9993943,0.00019436254,0.00022964316,0.000054863165,0.000049982213,0.00007678245],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.000520887,0.0005678978,0.00031793045,0.0012068725,0.0007689378,0.0004948178,0.00027571566,0.00034010026,0.0032076645],"category_scores_gemma":[0.0014970524,0.0001655926,0.0002565853,0.00084180245,0.0003721359,0.0001691188,0.00040797426,0.00021024782,0.0001764555],"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":[0.00069300283,0.00010462059,0.9442009,0.000057281446,0.00037027392,0.008863996,0.0008683275,0.00043440706,0.029125828,0.00054024236,0.00060548313,0.014135699],"study_design_scores_gemma":[0.00005763168,0.0000984922,0.9861224,0.000026880623,0.0001287432,0.007296533,0.00043819085,0.0010990098,0.0026069179,0.00049042085,0.0016193948,0.00001522812],"about_ca_topic_score_codex":0.0050388593,"about_ca_topic_score_gemma":0.0065713366,"teacher_disagreement_score":0.0050388593,"about_ca_system_score_codex":0.00014890179,"about_ca_system_score_gemma":0.00021764361,"threshold_uncertainty_score":0.010730684},"labels":[],"label_agreement":null},{"id":"W2904036412","doi":"10.1212/nxg.0000000000000296","title":"Screening of novel restless legs syndrome–associated genes in French-Canadian families","year":2018,"lang":"en","type":"article","venue":"Neurology Genetics","topic":"Restless Legs Syndrome Research","field":"Medicine","cited_by":13,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":true,"ca_institutions":"McGill University","funders":"Canadian Institutes of Health Research; Allergan; Idorsia Pharmaceuticals; ALS Association","keywords":"Locus (genetics); Gene; Genetics; Restless legs syndrome; Biology; Exome sequencing; Phenotype","score_opus":0.06101298094019582,"score_gpt":0.3234777698935873,"score_spread":0.2624647889533915,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2904036412","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99474984,0.000834483,0.00040476955,0.0002495259,0.000011387248,0.000023424553,0.0009661786,0.00002238226,0.0027379694],"genre_scores_gemma":[0.99626225,0.00053824094,0.0011920142,0.000109802866,0.0000095383775,0.00001361915,0.0006248341,0.000009608945,0.0012401389],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9996271,0.00003122714,0.00002198353,0.0000953046,0.00013708753,0.000087363296],"domain_scores_gemma":[0.9996251,0.00009919082,0.0000645607,0.000013287959,0.000121209465,0.00007666868],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00030182162,0.0008104089,0.00036946702,0.0017338754,0.0021569498,0.000660561,0.00068366365,0.0006100124,0.00406067],"category_scores_gemma":[0.0011966879,0.00022073282,0.0005215132,0.0015285522,0.00067634706,0.00015502035,0.00047999586,0.00033099987,0.00020453284],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":true,"about_ca_topic_consensus":true,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.001188682,0.00012903231,0.79734063,0.00036056445,0.00040895058,0.0614904,0.0057903575,0.0021024188,0.08198118,0.001980296,0.0035138885,0.04371354],"study_design_scores_gemma":[0.00009969413,0.00017205489,0.933395,0.00011376766,0.0003372641,0.040154696,0.0023315174,0.0013925593,0.008260599,0.00024977178,0.013431597,0.000061402374],"about_ca_topic_score_codex":0.6349488,"about_ca_topic_score_gemma":0.7200717,"teacher_disagreement_score":0.3650512,"about_ca_system_score_codex":0.0034109259,"about_ca_system_score_gemma":0.0034425342,"threshold_uncertainty_score":0.7344021},"labels":[],"label_agreement":null},{"id":"W2924785753","doi":"10.1212/nxg.0000000000000317","title":"Somatic expansion of the <i>C9orf72</i> hexanucleotide repeat does not occur in ALS spinal cord tissues","year":2019,"lang":"de","type":"article","venue":"Neurology Genetics","topic":"Amyotrophic Lateral Sclerosis Research","field":"Medicine","cited_by":10,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Health Sciences Centre; Sunnybrook Health Science Centre; Occupational Cancer Research Centre; Montreal Neurological Institute and Hospital","funders":"Schulich School of Medicine and Dentistry; University of Toronto; McGill University","keywords":"C9orf72; Amyotrophic lateral sclerosis; Biology; Trinucleotide repeat expansion; Spinal cord; Somatic cell; Anatomy; Genetics; Pathology; Medicine; Gene; Neuroscience; Disease","score_opus":0.026711237563850698,"score_gpt":0.3072437076161705,"score_spread":0.2805324700523198,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2924785753","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9963899,0.00017937273,0.0017399584,0.000032246975,0.000009948775,0.00002709929,0.00043033034,0.0000506662,0.0011404435],"genre_scores_gemma":[0.99680567,0.00008879724,0.0018606011,0.000046595185,0.0000047564636,0.000021641308,0.0006304148,0.000021650556,0.0005198865],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9997563,0.000020351103,0.00003872102,0.00008933648,0.00005012469,0.000045164546],"domain_scores_gemma":[0.9995746,0.0000860433,0.00014722528,0.00006694104,0.000063656786,0.000061506034],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00020623066,0.00020681157,0.00017087538,0.00028806625,0.00028577776,0.0002614796,0.00019846388,0.0003668701,0.0017493372],"category_scores_gemma":[0.00044567257,0.00017435553,0.00017622247,0.00018487991,0.00046436972,0.000116282805,0.0001430764,0.0002256757,0.00039764194],"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":[0.00019256247,0.000029931469,0.017810615,0.000046623016,0.000024445435,0.000984419,0.0000797287,0.000053891446,0.9790633,0.00005044276,0.00007460966,0.0015894407],"study_design_scores_gemma":[0.000033996443,0.00067115243,0.44257927,0.000030245135,0.000090641784,0.014106476,0.00030306377,0.00079851656,0.5393333,0.00015305995,0.0018855473,0.000014792929],"about_ca_topic_score_codex":0.0015274485,"about_ca_topic_score_gemma":0.0034558629,"teacher_disagreement_score":0.0017493372,"about_ca_system_score_codex":0.00014276772,"about_ca_system_score_gemma":0.000157469,"threshold_uncertainty_score":0.0058521032},"labels":[],"label_agreement":null},{"id":"W2943570569","doi":"10.1212/nxg.0000000000000336","title":"Hybrid gel electrophoresis using skin fibroblasts to aid in diagnosing mitochondrial disease","year":2019,"lang":"en","type":"article","venue":"Neurology Genetics","topic":"Mitochondrial Function and Pathology","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 Alberta Hospital; University of Calgary; University of Alberta","funders":"","keywords":"Mitochondrial DNA; Polyacrylamide gel electrophoresis; Skeletal muscle; Mitochondrial disease; Biopsy; Gel electrophoresis; Skin biopsy; Molecular biology; Biology; Muscle biopsy; Mitochondrion; Gene; Medicine; Pathology; Genetics; Biochemistry; Anatomy; Enzyme","score_opus":0.008076176848883747,"score_gpt":0.237594634537983,"score_spread":0.22951845768909923,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2943570569","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.7190922,0.006772952,0.26133934,0.00032153117,0.00032766335,0.0003226294,0.0006606593,0.0014379509,0.009725137],"genre_scores_gemma":[0.78924966,0.0023478062,0.2026603,0.00028586836,0.00006804223,0.0001921964,0.00084213674,0.00012758088,0.004226472],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99944,0.00015552875,0.0000484108,0.00018645267,0.0001373039,0.000032336193],"domain_scores_gemma":[0.99939716,0.00022258903,0.00008253069,0.00008565685,0.00014380134,0.00006827825],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00074496085,0.0006998282,0.00021871451,0.0008463128,0.000224269,0.00036071948,0.00036803453,0.00059973815,0.0018031005],"category_scores_gemma":[0.00054115267,0.00021695242,0.0002263301,0.00023250697,0.0003119412,0.00032086155,0.0004370606,0.00065594574,0.00093451375],"study_design_candidate":"bench_or_experimental","study_design_consensus":"bench_or_experimental","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00006850809,0.000027681168,0.0017814253,0.000057308647,0.000020979882,0.00028854646,0.000035347264,0.000047654023,0.9938643,0.00007561741,0.000049988925,0.0036827268],"study_design_scores_gemma":[0.000022019318,0.00039884745,0.018195026,0.00003461777,0.00007563595,0.009997992,0.00008403727,0.0025811226,0.9640097,0.00021775585,0.004360312,0.000022864873],"about_ca_topic_score_codex":0.0002776818,"about_ca_topic_score_gemma":0.0007250009,"teacher_disagreement_score":0.0018031005,"about_ca_system_score_codex":0.00011749448,"about_ca_system_score_gemma":0.00009794199,"threshold_uncertainty_score":0.00603199},"labels":[],"label_agreement":null},{"id":"W2944862706","doi":"10.1212/nxg.0000000000000338","title":"<i>DMPK</i> gene DNA methylation levels are associated with muscular and respiratory profiles in DM1","year":2019,"lang":"en","type":"article","venue":"Neurology Genetics","topic":"Genetic Neurodegenerative Diseases","field":"Neuroscience","cited_by":29,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Centre Intégré Universitaire de Santé et de Services Sociaux du Saguenay–Lac-Saint-Jean; Université de Sherbrooke","funders":"","keywords":"Myotonic dystrophy; CpG site; Internal medicine; Biology; DNA methylation; Medicine; Gene; Genetics; Cardiology; Gene expression","score_opus":0.03585328358144145,"score_gpt":0.25620635378869067,"score_spread":0.2203530702072492,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2944862706","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9994524,0.0000971085,0.00009275468,0.000013197368,8.669084e-7,0.0000017765005,0.00015948947,0.0000031178793,0.00017936177],"genre_scores_gemma":[0.999479,0.000030311578,0.000103536404,0.000009322223,0.00000196438,0.0000021888118,0.0001695847,0.0000016453116,0.00020253532],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9999138,0.000016701471,0.000009734043,0.000031390664,0.000014000108,0.000014321209],"domain_scores_gemma":[0.99979407,0.000050863986,0.00009158407,0.000009350755,0.000020030328,0.00003420377],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00014612234,0.00018343444,0.00012191658,0.00033739142,0.00013714301,0.00017409821,0.00009459233,0.00019083136,0.0024767795],"category_scores_gemma":[0.0005044292,0.00007923727,0.00008069015,0.0002012076,0.00012121088,0.00008157485,0.00016257324,0.00018487604,0.00023560575],"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":[0.00084199256,0.000031303858,0.95253175,0.000026436068,0.00007864837,0.00017915067,0.0001088699,0.00014254983,0.038196538,0.00004247571,0.00015623117,0.007663981],"study_design_scores_gemma":[0.000007705402,0.00008573373,0.9954568,0.0000039210804,0.000025495608,0.00093493366,0.000042480795,0.00019333772,0.003049809,0.000027193513,0.00017052544,0.0000021181186],"about_ca_topic_score_codex":0.0007249867,"about_ca_topic_score_gemma":0.0011934339,"teacher_disagreement_score":0.0024767795,"about_ca_system_score_codex":0.000116095005,"about_ca_system_score_gemma":0.000040034323,"threshold_uncertainty_score":0.008285642},"labels":[],"label_agreement":null},{"id":"W2959335923","doi":"10.1212/nxg.0000000000000348","title":"Genetic risk of Parkinson disease and progression:","year":2019,"lang":"en","type":"article","venue":"Neurology Genetics","topic":"Parkinson's Disease Mechanisms and Treatments","field":"Medicine","cited_by":162,"is_retracted":false,"has_abstract":true,"route_ca_aff":false,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"","funders":"National Center for Research Resources; National Human Genome Research Institute; National Institute on Aging; NIHR Cambridge Biomedical Research Centre; Helse Sør-Øst RHF; Medical Research Council; Parkinsonfonden; Allergan; National Institutes of Health; Voyager Therapeutics; National Institute for Health and Care Research; Agence Nationale de Sécurité du Médicament et des Produits de Santé; Centre National de la Recherche Scientifique; Evelyn Trust; Ipsen; Fonds Wetenschappelijk Onderzoek; Association France Parkinson; Assistance Publique - Hôpitaux de Paris; Institut National de la Santé et de la Recherche Médicale; Biogen; Agence Nationale de la Recherche; H. Lundbeck A/S; Rosetrees Trust; Parkinson's UK; Radboud Universiteit; Hersenstichting; Verily Life Sciences; GlaxoSmithKline; Barts Charity; Johns Hopkins University; Amarin Corporation; Michael J. Fox Foundation for Parkinson's Research; Parkinson's Foundation; Kinetics Foundation; Wellcome Trust; ZonMw; Britannia Pharmaceuticals; Weston Brain Institute; National Institute of Neurological Disorders and Stroke; Sunovion; Norges Forskningsråd; University of Virginia; National Parkinson Foundation; EU Joint Programme – Neurodegenerative Disease Research; Pfizer; University of Rochester; University of Pennsylvania; Brown University; CHDI Foundation; Massachusetts General Hospital; Smart Family Foundation; Parkinson's Disease Foundation; U.S. Department of Defense; Ohio State University; Harvard NeuroDiscovery Center; Parkinson Vereniging; Nasjonalforeningen for Folkehelsen; University of Michigan","keywords":"Allele; Odds ratio; Hazard ratio; LRRK2; Genotype; Internal medicine; Disease; Genetics; Medicine; Biology; Parkinson's disease; Confidence interval; Gene","score_opus":0.009533747352843087,"score_gpt":0.2584193033352295,"score_spread":0.2488855559823864,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2959335923","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99621326,0.001065681,0.0004649284,0.00024558368,0.000019585006,0.000018421973,0.0008025003,0.0000148594145,0.0011551409],"genre_scores_gemma":[0.9985348,0.0002101706,0.00027865582,0.00007539139,0.000033953536,0.000009991151,0.00039089215,0.0000034407333,0.00046274153],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99978906,0.000052562118,0.00001314479,0.000067843044,0.00004044442,0.000037059315],"domain_scores_gemma":[0.99961203,0.000064183354,0.00016483171,0.000028225155,0.00003677009,0.0000939155],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00038034856,0.00030122112,0.00027551412,0.0002958138,0.00024407102,0.00036539958,0.0002066584,0.00072331703,0.0025244097],"category_scores_gemma":[0.0009466841,0.00010077913,0.0005944261,0.00045147244,0.00017658377,0.00022486273,0.00027340034,0.000594799,0.00013210722],"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":[0.00079589075,0.00005968102,0.9877082,0.000038330465,0.00038828235,0.00030327198,0.00005212674,0.00021261271,0.0017287962,0.000088648085,0.00042972955,0.008194309],"study_design_scores_gemma":[0.000024868003,0.00012465406,0.9983089,0.000012743739,0.0000968421,0.0003894054,0.000023188108,0.000422533,0.00014639829,0.00014019097,0.00030648743,0.000003792661],"about_ca_topic_score_codex":0.005706221,"about_ca_topic_score_gemma":0.0072182505,"teacher_disagreement_score":0.005706221,"about_ca_system_score_codex":0.00016888851,"about_ca_system_score_gemma":0.00029896747,"threshold_uncertainty_score":0.011346042},"labels":[],"label_agreement":null},{"id":"W2966994499","doi":"10.1212/nxg.0000000000000354","title":"Genetic risk of Parkinson disease and progression: An analysis of 13 longitudinal cohorts","year":2019,"lang":"en","type":"erratum","venue":"Neurology Genetics","topic":"Parkinson's Disease Mechanisms and Treatments","field":"Medicine","cited_by":21,"is_retracted":false,"has_abstract":true,"route_ca_aff":false,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"","funders":"National Human Genome Research Institute; National Institute on Aging; NIHR Cambridge Biomedical Research Centre; Helse Sør-Øst RHF; Medical Research Council; Parkinsonfonden; Allergan; National Institutes of Health; Weston Brain Institute; Britannia Pharmaceuticals; Voyager Therapeutics; National Institute for Health and Care Research; Agence Nationale de Sécurité du Médicament et des Produits de Santé; Centre National de la Recherche Scientifique; Evelyn Trust; Ipsen; Fonds Wetenschappelijk Onderzoek; Association France Parkinson; Assistance Publique - Hôpitaux de Paris; Institut National de la Santé et de la Recherche Médicale; Biogen; Agence Nationale de la Recherche; H. Lundbeck A/S; Rosetrees Trust; Parkinson's UK; Radboud Universiteit; Hersenstichting; Verily Life Sciences; Johns Hopkins University; Amarin Corporation; Michael J. Fox Foundation for Parkinson's Research; Parkinson's Foundation; Kinetics Foundation; Wellcome Trust; ZonMw; National Institute of Neurological Disorders and Stroke; Sunovion; Norges Forskningsråd; University of Virginia; National Parkinson Foundation; EU Joint Programme – Neurodegenerative Disease Research; Pfizer; University of Rochester; University of Pennsylvania; Brown University; CHDI Foundation; Massachusetts General Hospital; GlaxoSmithKline; Smart Family Foundation; Parkinson's Disease Foundation; U.S. Department of Defense; Ohio State University; Harvard NeuroDiscovery Center; Parkinson Vereniging; Nasjonalforeningen for Folkehelsen; University of Michigan","keywords":"Disease; Medicine; Internal medicine","score_opus":0.014712288669985725,"score_gpt":0.2847142190027348,"score_spread":0.27000193033274905,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2966994499","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9337141,0.015195755,0.004433595,0.009498815,0.004942586,0.00006733991,0.027510738,0.00016085073,0.004476261],"genre_scores_gemma":[0.9704724,0.00473547,0.0033183026,0.0020075752,0.0009318662,0.0001318511,0.009995205,0.000092570255,0.008314698],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99912757,0.00027613217,0.00015892151,0.00021765022,0.00015031412,0.00006946939],"domain_scores_gemma":[0.9968696,0.0013290541,0.0006905097,0.00048812336,0.00045414126,0.00016850118],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0024429231,0.00033521108,0.00053126324,0.00054219837,0.000609147,0.0005627614,0.00052410876,0.00074707874,0.0034280235],"category_scores_gemma":[0.008721454,0.00023889243,0.0010284529,0.0016467284,0.00018615919,0.00030738066,0.00047148907,0.0010580588,0.00034448763],"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":[0.0019723636,0.00005035862,0.9319991,0.00015747287,0.001833892,0.0014103161,0.0002667067,0.00028175864,0.00036151378,0.00060079416,0.03610204,0.024963608],"study_design_scores_gemma":[0.0003608395,0.0002604317,0.9809109,0.00014024256,0.002410372,0.0025396345,0.00020520505,0.00076008507,0.00025074888,0.000785801,0.0113231065,0.00005264264],"about_ca_topic_score_codex":0.012812918,"about_ca_topic_score_gemma":0.016387576,"teacher_disagreement_score":0.012812918,"about_ca_system_score_codex":0.0003343605,"about_ca_system_score_gemma":0.0005806429,"threshold_uncertainty_score":0.025476694},"labels":[],"label_agreement":null},{"id":"W2971801552","doi":"10.1212/nxg.0000000000000359","title":"Homozygous pathogenic variant in <i>BRAT1</i> associated with nonprogressive cerebellar ataxia","year":2019,"lang":"en","type":"article","venue":"Neurology Genetics","topic":"Mitochondrial Function and Pathology","field":"Biochemistry, Genetics and Molecular Biology","cited_by":17,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"SickKids Foundation; Hospital for Sick Children; Montreal Children's Hospital; University of Toronto","funders":"University of Toronto; McGill University; Grantová Agentura, Univerzita Karlova; University of Ottawa; Univerzita Karlova v Praze","keywords":"Ataxia-telangiectasia; Biology; Ataxia; Cerebellar ataxia; Kinase; Phosphorylation; Blot; Protein subunit; Cell culture; Cerebellum; Molecular biology; Genetics; Cancer research; Endocrinology; Neuroscience; Gene","score_opus":0.005715511882440145,"score_gpt":0.20412168332104175,"score_spread":0.1984061714386016,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2971801552","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99745184,0.00023007019,0.0010105552,0.00009506909,0.000022927847,0.00002674164,0.00035918754,0.000058068697,0.00074540894],"genre_scores_gemma":[0.99854136,0.00010554293,0.00060624426,0.000059424998,0.00002568764,0.000012543117,0.00026953284,0.000019838193,0.00035983065],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.99975747,0.000021492697,0.00003314219,0.00009640225,0.000059959042,0.00003153653],"domain_scores_gemma":[0.99969816,0.00008301274,0.00010170575,0.000023441093,0.00002249495,0.00007117548],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00011475278,0.0009942609,0.00040271724,0.0004198958,0.0004649092,0.000327803,0.00045295464,0.000924172,0.002887146],"category_scores_gemma":[0.00060546544,0.00016438973,0.00032122392,0.0003142174,0.0004671376,0.0001920474,0.0003664063,0.00047953855,0.00050992926],"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":[0.0006318637,0.00022509757,0.089101374,0.00020047474,0.00011760187,0.39954045,0.000897955,0.00048099578,0.4979867,0.00051137735,0.0010124509,0.009293557],"study_design_scores_gemma":[0.00009004001,0.00079141156,0.23550008,0.000048345843,0.00016622127,0.6965296,0.0003316123,0.0014043237,0.060840614,0.0003488255,0.0038979687,0.00005093363],"about_ca_topic_score_codex":0.0006409819,"about_ca_topic_score_gemma":0.0007197905,"teacher_disagreement_score":0.002887146,"about_ca_system_score_codex":0.00020630323,"about_ca_system_score_gemma":0.00014070306,"threshold_uncertainty_score":0.009658515},"labels":[],"label_agreement":null},{"id":"W2982618970","doi":"10.1212/nxg.0000000000000369","title":"Clinical spectrum of POLR3-related leukodystrophy caused by biallelic <i>POLR1C</i> pathogenic variants","year":2019,"lang":"en","type":"article","venue":"Neurology Genetics","topic":"RNA regulation and disease","field":"Biochemistry, Genetics and Molecular Biology","cited_by":50,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"SickKids Foundation; McGill University Health Centre; Hospital for Sick Children; Montreal Children's Hospital; University of Toronto","funders":"Canadian Institutes of Health Research","keywords":"Leukodystrophy; Hyperintensity; Medicine; Cohort; Craniofacial; Pathology; Pediatrics; Internal medicine; Disease; Magnetic resonance imaging; Radiology","score_opus":0.008031341854042287,"score_gpt":0.2510854476399408,"score_spread":0.2430541057858985,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2982618970","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99913067,0.0001322095,0.0001292649,0.00001602611,0.0000013617491,0.000010999994,0.000110050874,0.000009764785,0.00045977623],"genre_scores_gemma":[0.9996784,0.00004117334,0.000114009286,0.000019192574,0.0000059351073,0.0000036986416,0.00009561437,0.0000022568543,0.000039626542],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9997044,0.000053287054,0.00005767587,0.000086572654,0.00003786655,0.000060066486],"domain_scores_gemma":[0.9993647,0.00014754472,0.00027886053,0.000024763242,0.000039824296,0.00014438535],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0003814128,0.0005110842,0.00032315878,0.00065585226,0.00036006205,0.00032403556,0.00024384238,0.00041355574,0.0028220492],"category_scores_gemma":[0.000918625,0.00023446465,0.00020644059,0.00048255987,0.00047742133,0.00029807468,0.00042321553,0.00020869993,0.00033541775],"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":[0.00046165643,0.00006613815,0.9703387,0.000028317667,0.000039043174,0.01508774,0.0001889187,0.00006509024,0.010466248,0.000054442167,0.00013746906,0.0030662867],"study_design_scores_gemma":[0.000034456265,0.0004265879,0.9197729,0.000018693589,0.00003455011,0.07774089,0.00036890458,0.00017667325,0.0011187646,0.000085881344,0.00021193553,0.000009625755],"about_ca_topic_score_codex":0.0010632576,"about_ca_topic_score_gemma":0.0010690194,"teacher_disagreement_score":0.0028220492,"about_ca_system_score_codex":0.00014103686,"about_ca_system_score_gemma":0.00020872103,"threshold_uncertainty_score":0.0094406605},"labels":[],"label_agreement":null},{"id":"W2993831323","doi":"10.1212/nxg.0000000000000378","title":"Critical exon indexing improves clinical interpretation of copy number variants in neurodevelopmental disorders","year":2019,"lang":"en","type":"article","venue":"Neurology Genetics","topic":"Genomics and Rare Diseases","field":"Biochemistry, Genetics and Molecular Biology","cited_by":5,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"SickKids Foundation; Hospital for Sick Children; University of Toronto","funders":"Canadian Institutes of Health Research; Hospital for Sick Children; University of Toronto; GlaxoSmithKline","keywords":"Copy-number variation; Clinical significance; OMIM : Online Mendelian Inheritance in Man; Mendelian inheritance; Genetics; Gene duplication; Exon; Relevance (law); Medicine; Biology; Gene; Bioinformatics; Genome; Phenotype; Pathology","score_opus":0.006903764828108048,"score_gpt":0.29151439611518765,"score_spread":0.2846106312870796,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2993831323","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9261458,0.0024290946,0.057756923,0.00093006616,0.00017141394,0.00049591064,0.002741603,0.0026719202,0.006657202],"genre_scores_gemma":[0.88327014,0.00041999997,0.11368557,0.00020001385,0.00013463199,0.00012380864,0.0011418547,0.0001491766,0.00087481685],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99784935,0.00083772844,0.00033756447,0.00034685232,0.00051527395,0.00011315893],"domain_scores_gemma":[0.9836998,0.010683855,0.0019014473,0.0009268191,0.002286722,0.00050136936],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0057988004,0.00061106915,0.0005115794,0.003694162,0.00033909874,0.0014576154,0.000646584,0.0005745074,0.004079426],"category_scores_gemma":[0.027660714,0.00020800623,0.00031418205,0.0015137143,0.0004607115,0.00088275055,0.0009839057,0.0004395537,0.0008657983],"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":[0.00275359,0.0002398366,0.58745223,0.00034067457,0.00015192656,0.00070589146,0.0004902781,0.0025163935,0.030768706,0.00075737096,0.0063975463,0.36742544],"study_design_scores_gemma":[0.0002279277,0.0010395568,0.8453635,0.000204883,0.00035902028,0.0062066168,0.0006363492,0.059984613,0.072487295,0.002798191,0.010525223,0.00016678743],"about_ca_topic_score_codex":0.0025057052,"about_ca_topic_score_gemma":0.0035997303,"teacher_disagreement_score":0.0057988004,"about_ca_system_score_codex":0.00048061874,"about_ca_system_score_gemma":0.0007167954,"threshold_uncertainty_score":0.030667365},"labels":[],"label_agreement":null},{"id":"W2997137838","doi":"10.1212/nxg.0000000000000389","title":"HSAN-VI","year":2020,"lang":"en","type":"article","venue":"Neurology Genetics","topic":"Skin and Cellular Biology Research","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 Ottawa","funders":"","keywords":"Gene isoform; Null allele; Dystonia; Allele; Pathogenesis; Mutation; Gene; Disease; Compound heterozygosity; Genetics; Biology; Medicine; Immunology; Pathology; Neuroscience","score_opus":0.022165968067160036,"score_gpt":0.26810145387146095,"score_spread":0.2459354858043009,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2997137838","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9556928,0.0025058223,0.0045519015,0.0002572731,0.0002681508,0.000095933705,0.00207033,0.000312363,0.034245297],"genre_scores_gemma":[0.9453282,0.0011240355,0.0034440157,0.00028161678,0.000045374807,0.00004447436,0.004682233,0.00007083219,0.044979177],"study_design_codex":"bench_or_experimental","study_design_gemma":"not_applicable","domain_scores_codex":[0.99992514,0.0000064639694,0.000005665776,0.00002386646,0.000025254109,0.000013511983],"domain_scores_gemma":[0.99994147,0.0000038623207,0.000010066768,0.0000077898785,0.000010981897,0.000025853882],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.000078728866,0.00025480665,0.00013018094,0.00020708743,0.00023419276,0.00022948199,0.00021146637,0.0002888484,0.007628538],"category_scores_gemma":[0.0001610541,0.00006927962,0.00019006451,0.00012414235,0.0001380682,0.00013385633,0.00030350103,0.0002659517,0.0026679616],"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":[0.00033502217,0.00008326416,0.010449883,0.0002419545,0.000041890256,0.0040847627,0.00011658309,0.00021250307,0.9327885,0.0029747149,0.0041813585,0.04448947],"study_design_scores_gemma":[0.00010346737,0.0019166144,0.1722938,0.0001302497,0.00010461785,0.099840075,0.00025653324,0.0023398048,0.45782644,0.0034064257,0.26173967,0.000042305004],"about_ca_topic_score_codex":0.00034911177,"about_ca_topic_score_gemma":0.00045587352,"teacher_disagreement_score":0.007628538,"about_ca_system_score_codex":0.00019418186,"about_ca_system_score_gemma":0.00013072092,"threshold_uncertainty_score":0},"labels":[],"label_agreement":null},{"id":"W2999634369","doi":"10.1212/nxg.0000000000000392","title":"<i>COL4A1</i> -related autosomal recessive encephalopathy in 2 Turkish children","year":2020,"lang":"en","type":"article","venue":"Neurology Genetics","topic":"Cerebrovascular and genetic 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":"Children's Hospital of Eastern Ontario","funders":"National Human Genome Research Institute; Türkiye Bilimsel ve Teknolojik Araştırma Kurumu; Medical Research Council; Newton Fund; Vrije Universiteit Amsterdam; Wellcome Trust","keywords":"Leukoencephalopathy; Missense mutation; Penetrance; Exome sequencing; Medicine; Genetics; Disease gene identification; Compound heterozygosity; Encephalopathy; Consanguinity; Disease; Pediatrics; Global developmental delay; Phenotype; Pathology; Biology; Internal medicine; Gene","score_opus":0.007529697851358078,"score_gpt":0.2249201535045728,"score_spread":0.21739045565321474,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2999634369","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9982451,0.0002524624,0.00033872956,0.00012333592,0.000032477354,0.00003113868,0.0002191769,0.00003163954,0.00072591973],"genre_scores_gemma":[0.9981641,0.00020277413,0.0006873178,0.00019194315,0.000034227793,0.000018342515,0.00021915809,0.000027624013,0.0004544037],"study_design_codex":"case_report","study_design_gemma":"case_report","domain_scores_codex":[0.9996112,0.00003225164,0.000052961605,0.00015217788,0.000061112216,0.00009035299],"domain_scores_gemma":[0.999616,0.00007551608,0.00012111408,0.000018101833,0.00003444418,0.00013486123],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00018077315,0.0018690554,0.00058354845,0.001079613,0.001185071,0.00050199684,0.00044716347,0.0011722981,0.0022670643],"category_scores_gemma":[0.0009988653,0.00061568216,0.00074412936,0.00069357007,0.00076460995,0.00040258115,0.00096775184,0.0007284558,0.0003274419],"study_design_candidate":"case_report","study_design_consensus":"case_report","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00033239104,0.00017763772,0.16536285,0.00013012115,0.00011389747,0.8024664,0.0018035494,0.00028924044,0.019932026,0.00038516836,0.0011483026,0.007858386],"study_design_scores_gemma":[0.000059623962,0.0003271515,0.2264038,0.00005537534,0.00009769329,0.76749057,0.00080132595,0.0003783633,0.0022014212,0.0002497809,0.0018858489,0.000049066297],"about_ca_topic_score_codex":0.00661842,"about_ca_topic_score_gemma":0.0066078417,"teacher_disagreement_score":0.00661842,"about_ca_system_score_codex":0.0006307936,"about_ca_system_score_gemma":0.00060794986,"threshold_uncertainty_score":0.013159752},"labels":[],"label_agreement":null},{"id":"W3000447669","doi":"10.1212/nxg.0000000000000385","title":"Analysis of common and rare <i>VPS13C</i> variants in late-onset Parkinson disease","year":2020,"lang":"en","type":"article","venue":"Neurology Genetics","topic":"Parkinson's Disease Mechanisms and Treatments","field":"Medicine","cited_by":29,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"McGill University","funders":"National Center for Advancing Translational Sciences; National Institute of Neurological Disorders and Stroke; Canadian Glycomics Network; Consortium canadien en neurodégénérescence associée au vieillissement; Michael J. Fox Foundation for Parkinson's Research","keywords":"Haplotype; Odds ratio; Linkage disequilibrium; Minor allele frequency; Allele; Genetics; SNP; Compound heterozygosity; Genetic association; Medicine; Biology; Internal medicine; Genotype; Single-nucleotide polymorphism; Allele frequency; Gene","score_opus":0.01939717067471292,"score_gpt":0.2597685898616456,"score_spread":0.24037141918693267,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W3000447669","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9748218,0.02083775,0.0016710234,0.00025861838,0.00006672522,0.00002288765,0.0016484477,0.000041702526,0.00063097186],"genre_scores_gemma":[0.99745935,0.0014162038,0.00038817548,0.000089831905,0.000043786047,0.000010541072,0.00046150555,0.000012020018,0.00011865641],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9989857,0.00027193257,0.00012068443,0.00042707974,0.00012810723,0.00006647492],"domain_scores_gemma":[0.9979303,0.0010712533,0.0004929735,0.00020130328,0.00015334968,0.00015087347],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0019539914,0.0006224043,0.00086743035,0.0011738072,0.00044122897,0.0008764325,0.00054245867,0.00082892907,0.0014875812],"category_scores_gemma":[0.0027747906,0.0003422998,0.0029552546,0.0019144736,0.0004006569,0.0002686813,0.0004580661,0.00053811615,0.00015105374],"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":[0.003631603,0.000040655363,0.94686997,0.0006975747,0.022904541,0.0010083169,0.00014295617,0.0012163551,0.0065284222,0.00016996244,0.00069673895,0.016092958],"study_design_scores_gemma":[0.0003401324,0.00046192732,0.9697667,0.00018068671,0.020655066,0.0015015891,0.0001273871,0.0027618057,0.0016179045,0.000597337,0.0019614964,0.000027988575],"about_ca_topic_score_codex":0.005243314,"about_ca_topic_score_gemma":0.0062057017,"teacher_disagreement_score":0.005243314,"about_ca_system_score_codex":0.00027330185,"about_ca_system_score_gemma":0.0003238583,"threshold_uncertainty_score":0.010425568},"labels":[],"label_agreement":null},{"id":"W3008325827","doi":"10.1212/nxg.0000000000000403","title":"Characterization of the phenotype with cognitive impairment and protein mislocalization in SCA34","year":2020,"lang":"en","type":"article","venue":"Neurology Genetics","topic":"RNA regulation and disease","field":"Biochemistry, Genetics and Molecular Biology","cited_by":34,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":true,"ca_institutions":"Université Laval; Centre hospitalier de l'Université Laval; Université du Québec à Montréal","funders":"Université Laval","keywords":"Dysmetria; Ataxia; Dysarthria; Cerebellar ataxia; Pathology; Cerebellum; Atrophy; Medicine; Spinocerebellar ataxia; Cognitive deficit; Psychology; Neuroscience; Audiology; Cognitive impairment; Disease","score_opus":0.0064184163306168635,"score_gpt":0.20387990989479923,"score_spread":0.19746149356418236,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W3008325827","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9991487,0.00013260826,0.00019510639,0.000020090703,0.0000014957469,0.000007735808,0.00007650173,0.000011586008,0.00040614247],"genre_scores_gemma":[0.99913424,0.000060143626,0.00036704735,0.000012915909,0.000003219175,0.0000033646022,0.00012097238,0.0000031172433,0.00029504523],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9999286,0.000007193499,0.0000055534333,0.000017135902,0.000025197565,0.000016346126],"domain_scores_gemma":[0.999894,0.000013191369,0.000030730407,0.0000060521907,0.000023111666,0.000032875407],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00012395688,0.00057847676,0.000117918404,0.00055551674,0.0003234266,0.0001891232,0.00020290841,0.00034057721,0.001190838],"category_scores_gemma":[0.00030018244,0.000071799914,0.00012900196,0.00022305048,0.00029762712,0.0000667171,0.00011390364,0.00017190479,0.00014172873],"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":[0.00044055103,0.00017571602,0.31067017,0.00012529556,0.00009347431,0.066848285,0.00084888353,0.00049910217,0.6056749,0.0002687649,0.00059359556,0.013761206],"study_design_scores_gemma":[0.000041333493,0.00036493642,0.8571797,0.000025217812,0.000072846466,0.11601127,0.00026791726,0.0010080514,0.023012478,0.00009516313,0.0019039924,0.000017172946],"about_ca_topic_score_codex":0.016493998,"about_ca_topic_score_gemma":0.02405381,"teacher_disagreement_score":0.016493998,"about_ca_system_score_codex":0.00042799747,"about_ca_system_score_gemma":0.0003936688,"threshold_uncertainty_score":0.032796025},"labels":[],"label_agreement":null},{"id":"W3010841610","doi":"10.1212/nxg.0000000000000409","title":"4H leukodystrophy","year":2020,"lang":"en","type":"article","venue":"Neurology Genetics","topic":"RNA regulation and disease","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":"McGill University; McGill University Health Centre; University of Ottawa","funders":"","keywords":"Leukodystrophy; Hypodontia; Medicine; Hypogonadotropic hypogonadism; Pediatrics; Genetics; Disease; Pathology; Biology; Internal medicine; Orthodontics","score_opus":0.012909526700191349,"score_gpt":0.2293438822715718,"score_spread":0.21643435557138044,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W3010841610","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.8671691,0.008559331,0.0048807804,0.0019351287,0.00052102504,0.00047505065,0.00605624,0.000988704,0.109414674],"genre_scores_gemma":[0.952598,0.0016825226,0.0017013671,0.0018137145,0.00017058829,0.00008612704,0.002026253,0.00010981328,0.039811704],"study_design_codex":"case_report","study_design_gemma":"case_report","domain_scores_codex":[0.9998443,0.00001961121,0.000011759013,0.000038663176,0.000033493616,0.000052121995],"domain_scores_gemma":[0.9998915,0.000021473734,0.00002087685,0.000011962825,0.000013697655,0.000040441857],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00012024295,0.00067256397,0.00041078607,0.0006121965,0.00060194806,0.00038088684,0.00036007393,0.00068483676,0.02165136],"category_scores_gemma":[0.00036637782,0.000113051836,0.0002791646,0.00027572276,0.0004257807,0.00019883663,0.00043440994,0.0004127757,0.003343196],"study_design_candidate":"case_report","study_design_consensus":"case_report","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0014730702,0.00046198588,0.04716239,0.00061558443,0.00015902096,0.39834112,0.0010529972,0.0004810034,0.38171872,0.011814089,0.017557113,0.13916296],"study_design_scores_gemma":[0.0002568451,0.0007086575,0.09260757,0.00014558405,0.00012800418,0.69456303,0.00030636668,0.00046100037,0.046492163,0.0032445542,0.16101941,0.000066836685],"about_ca_topic_score_codex":0.0013340712,"about_ca_topic_score_gemma":0.0009942501,"teacher_disagreement_score":0.02165136,"about_ca_system_score_codex":0.00042500978,"about_ca_system_score_gemma":0.00023229957,"threshold_uncertainty_score":0.07243103},"labels":[],"label_agreement":null},{"id":"W3012413712","doi":"10.1212/nxg.0000000000000408","title":"Molecular diagnosis of muscular diseases in outpatient clinics","year":2020,"lang":"en","type":"article","venue":"Neurology Genetics","topic":"Genomics and Rare Diseases","field":"Biochemistry, Genetics and Molecular Biology","cited_by":17,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":true,"ca_institutions":"Université de Sherbrooke","funders":"Génome Québec; Fonds de Recherche du Québec - Santé; Sanofi Genzyme; Compute Canada; Sanofi","keywords":"Medicine; Outpatient clinic; Pediatrics; Internal medicine","score_opus":0.009930218427710477,"score_gpt":0.24039565121034917,"score_spread":0.2304654327826387,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W3012413712","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9976973,0.00045841746,0.00020265802,0.00013426955,0.000010679659,0.000026973205,0.0003937349,0.000019735695,0.0010562391],"genre_scores_gemma":[0.998228,0.00025617878,0.0007118025,0.00014775096,0.0000145672075,0.000009366529,0.00042014619,0.0000051741245,0.00020700613],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99914443,0.00018352344,0.00007204566,0.00017074126,0.00028823462,0.00014099506],"domain_scores_gemma":[0.9978527,0.0006665206,0.00053803495,0.000073005,0.00053115736,0.00033866093],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00076911226,0.00041409323,0.0003128973,0.0009733555,0.0005024842,0.0006497286,0.0005240913,0.00046070645,0.0023529038],"category_scores_gemma":[0.0050709858,0.0001992361,0.00017528402,0.00058555644,0.0003217833,0.00018278946,0.00044561224,0.0003134162,0.000403585],"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":[0.00015044918,0.000040011055,0.9900529,0.000033155877,0.000016613445,0.0016074555,0.00013619056,0.00012767957,0.0021738631,0.000021693759,0.00046457408,0.0051755738],"study_design_scores_gemma":[0.000034754226,0.00021364861,0.9874535,0.00005618784,0.000035534726,0.008087385,0.00041113963,0.0010050099,0.0017604997,0.00003103807,0.0009025439,0.000008806071],"about_ca_topic_score_codex":0.043997195,"about_ca_topic_score_gemma":0.047741137,"teacher_disagreement_score":0.043997195,"about_ca_system_score_codex":0.0010300546,"about_ca_system_score_gemma":0.0010993336,"threshold_uncertainty_score":0.087482214},"labels":[],"label_agreement":null},{"id":"W3013175781","doi":"10.1212/nxg.0000000000000416","title":"Polygenic risk scores of several subtypes of epilepsies in a founder population","year":2020,"lang":"en","type":"article","venue":"Neurology Genetics","topic":"Genomics and Rare Diseases","field":"Biochemistry, Genetics and Molecular Biology","cited_by":30,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":true,"ca_institutions":"Université de Montréal; Université du Québec à Montréal; Université du Québec à Chicoutimi","funders":"Compute Canada","keywords":"Epilepsy; Population; Medicine; Disease; Logistic regression; Internal medicine; Psychiatry","score_opus":0.009331983291852345,"score_gpt":0.22405015531207306,"score_spread":0.21471817202022073,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W3013175781","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9975446,0.0001265099,0.0011699755,0.000109458764,0.000005127399,0.000011636805,0.00049725326,0.000021692738,0.0005136814],"genre_scores_gemma":[0.9984686,0.000055071498,0.0007911792,0.000019445448,0.000008177485,0.000005882343,0.00043006704,0.0000067390606,0.00021482506],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99931717,0.00024975336,0.000047872454,0.00021194352,0.000095509306,0.00007777041],"domain_scores_gemma":[0.99828076,0.00064257503,0.00040536147,0.00033382818,0.0001814191,0.00015613671],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0016817253,0.0004426162,0.00024644093,0.0012670368,0.00041024212,0.00047350596,0.00033413235,0.00034021845,0.0023880294],"category_scores_gemma":[0.0040470893,0.00013707869,0.00090774597,0.0009895128,0.0004367628,0.00020830552,0.0003547974,0.0003337554,0.00015639997],"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":[0.00023110541,0.000014866013,0.99070156,0.000008310504,0.00045927806,0.00024032858,0.00016233059,0.000697347,0.0013899346,0.0003974728,0.00024313967,0.005454202],"study_design_scores_gemma":[0.000008860532,0.00005379058,0.99709344,0.0000029532782,0.0001408626,0.0003067622,0.00007791593,0.0017131856,0.00012798731,0.00026095816,0.00020541096,0.0000078151725],"about_ca_topic_score_codex":0.08673681,"about_ca_topic_score_gemma":0.05215151,"teacher_disagreement_score":0.08673681,"about_ca_system_score_codex":0.0004921139,"about_ca_system_score_gemma":0.00062694243,"threshold_uncertainty_score":0.1724639},"labels":[],"label_agreement":null},{"id":"W3023713429","doi":"10.1212/nxg.0000000000000425","title":"Expanding the phenotypic and molecular spectrum of RNA polymerase III–related leukodystrophy","year":2020,"lang":"en","type":"article","venue":"Neurology Genetics","topic":"RNA regulation and disease","field":"Biochemistry, Genetics and Molecular Biology","cited_by":36,"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":"Fondation des Etoiles; McGill University","keywords":"Leukodystrophy; Phenotype; Polymerase; Genetics; Biology; Virology; Medicine; Gene; Pathology; Disease","score_opus":0.006877537222865377,"score_gpt":0.21841018651988073,"score_spread":0.21153264929701535,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W3023713429","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99829394,0.00016318323,0.0005301625,0.000058555896,0.00000236289,0.000014614229,0.000101181686,0.000020588583,0.0008154459],"genre_scores_gemma":[0.99867815,0.00012478512,0.0009241676,0.000063573614,0.000016620585,0.0000063274297,0.000107972635,0.000008186664,0.00007008828],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.999691,0.00007527977,0.000049139933,0.000083240775,0.000050505325,0.000050880233],"domain_scores_gemma":[0.99960405,0.00010953757,0.00014012567,0.0000355433,0.000029957728,0.000080850696],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0003517607,0.0007126426,0.0003130292,0.0007463725,0.00023832096,0.00028533343,0.00023059157,0.00045127448,0.0013004105],"category_scores_gemma":[0.00070853444,0.00019929465,0.00031877053,0.00039568247,0.0004541884,0.0002969537,0.00051125133,0.00036764194,0.00020150191],"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":[0.0007649015,0.00016564337,0.72754383,0.00014246542,0.00009684088,0.06781718,0.00057300914,0.0008614738,0.17089438,0.0007907363,0.000473694,0.02987576],"study_design_scores_gemma":[0.000055100332,0.00045945658,0.7339244,0.00003528251,0.000044812143,0.25552177,0.0002777285,0.00085531274,0.007314434,0.00046036407,0.00102986,0.000021609974],"about_ca_topic_score_codex":0.00052384235,"about_ca_topic_score_gemma":0.00074339996,"teacher_disagreement_score":0.0013004105,"about_ca_system_score_codex":0.00013913926,"about_ca_system_score_gemma":0.00018469244,"threshold_uncertainty_score":0.004350364},"labels":[],"label_agreement":null},{"id":"W3033954889","doi":"10.1212/nxg.0000000000000452","title":"A splice variant in <i>ATAD3A</i> expands the clinical and genetic spectrum of Harel-Yoon syndrome","year":2020,"lang":"en","type":"article","venue":"Neurology Genetics","topic":"RNA regulation and disease","field":"Biochemistry, Genetics and Molecular Biology","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":"Newborn Screening Ontario; Children's Hospital of Eastern Ontario","funders":"","keywords":"Missense mutation; Atrophy; Hypotonia; Encephalopathy; Testicular atrophy; Genotype; Mitochondrion; Biology; Genetics; Neuroscience; Medicine; Phenotype; Internal medicine; Endocrinology; Gene","score_opus":0.018540294373402866,"score_gpt":0.2663682301213582,"score_spread":0.2478279357479553,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W3033954889","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.96787775,0.0011038245,0.0066169016,0.0014907452,0.0004617406,0.00018890614,0.0013198456,0.0004890884,0.020451225],"genre_scores_gemma":[0.9894028,0.00045147183,0.0057474785,0.00093249907,0.00048717292,0.0000496498,0.0007527875,0.00014205054,0.0020341564],"study_design_codex":"case_report","study_design_gemma":"case_report","domain_scores_codex":[0.9996728,0.00005355507,0.000047162408,0.00008091319,0.00009487682,0.00005066693],"domain_scores_gemma":[0.9992791,0.00026491148,0.00014541516,0.00004942517,0.00008098267,0.00018014555],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00036179606,0.0021559433,0.0007999704,0.0011401632,0.00078459235,0.00046175416,0.0006468993,0.0012614147,0.007233401],"category_scores_gemma":[0.0011405292,0.00024534095,0.0006281769,0.0010840503,0.0009398636,0.00034975505,0.00068258226,0.00083102996,0.0014424388],"study_design_candidate":"case_report","study_design_consensus":"case_report","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0008056751,0.00031462233,0.084072895,0.0002072511,0.00015248531,0.693929,0.000734065,0.00064474944,0.1649478,0.0038699447,0.0067026615,0.043618973],"study_design_scores_gemma":[0.00015683683,0.00039621923,0.11858287,0.00015081542,0.00015821442,0.85447216,0.00030189764,0.0012820559,0.008034563,0.0028741525,0.013529437,0.000060773546],"about_ca_topic_score_codex":0.0022672184,"about_ca_topic_score_gemma":0.004111077,"teacher_disagreement_score":0.007233401,"about_ca_system_score_codex":0.00026716525,"about_ca_system_score_gemma":0.0004213903,"threshold_uncertainty_score":0.024198174},"labels":[],"label_agreement":null},{"id":"W3084271221","doi":"10.1212/nxg.0000000000000515","title":"Novel dominant MPAN family with a complex genetic architecture as a basis for phenotypic variability","year":2020,"lang":"en","type":"article","venue":"Neurology Genetics","topic":"Neurological diseases and metabolism","field":"Neuroscience","cited_by":18,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Occupational Cancer Research Centre; University of Toronto; University Health Network","funders":"","keywords":"Biology; Parkinsonism; Phenotype; Genetics; Neurodegeneration; Multiplex ligation-dependent probe amplification; Tauopathy; Genetic architecture; Gene; Pathology; Medicine; Disease; Exon","score_opus":0.05290714783277106,"score_gpt":0.26745301483741224,"score_spread":0.21454586700464118,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W3084271221","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99734926,0.00013708856,0.0012230986,0.000094290874,0.0000063508123,0.000012417957,0.00018868329,0.000043765103,0.0009451167],"genre_scores_gemma":[0.9982394,0.000061522085,0.0012295842,0.00006197641,0.000017249316,0.0000094403595,0.00012391388,0.00001603212,0.00024080483],"study_design_codex":"case_report","study_design_gemma":"observational","domain_scores_codex":[0.9998393,0.000027603033,0.000015275202,0.00007547081,0.000022922311,0.000019437837],"domain_scores_gemma":[0.9998053,0.000072250725,0.000057059606,0.000020415413,0.0000109105795,0.00003399985],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00014888107,0.0006656893,0.0003916221,0.00046463448,0.00040478737,0.00025075607,0.00031752937,0.00042114532,0.001999238],"category_scores_gemma":[0.0006102645,0.00023276293,0.00026296565,0.00040919028,0.00045661637,0.00016842005,0.0004755385,0.00028904097,0.0001882203],"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":[0.0011891383,0.00018381262,0.23828304,0.00017960805,0.00022343246,0.5780999,0.0012563325,0.0014738409,0.14420177,0.0024837933,0.0013903363,0.03103502],"study_design_scores_gemma":[0.00007635065,0.00023219317,0.3103647,0.000033596607,0.00008993388,0.6770438,0.00019264163,0.0025303522,0.005486947,0.0009525959,0.0029571997,0.000039568888],"about_ca_topic_score_codex":0.000638616,"about_ca_topic_score_gemma":0.0008095773,"teacher_disagreement_score":0.001999238,"about_ca_system_score_codex":0.0001900192,"about_ca_system_score_gemma":0.00016260767,"threshold_uncertainty_score":0.0066880584},"labels":[],"label_agreement":null},{"id":"W3091886723","doi":"10.1212/nxg.0000000000000512","title":"Late-onset vs nonmendelian early-onset Alzheimer disease","year":2020,"lang":"en","type":"review","venue":"Neurology Genetics","topic":"Alzheimer's disease research and treatments","field":"Medicine","cited_by":170,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Occupational Cancer Research Centre; University of Toronto","funders":"National Institute on Aging","keywords":"Disease; Alzheimer's disease; Neuroimaging; Categorization; Age of onset; Early-onset Alzheimer's disease; Etiology; Neuroscience; Clinical phenotype; Medicine; Bioinformatics; Phenotype; Psychology; Biology; Pathology; Genetics; Gene","score_opus":0.07202862882385688,"score_gpt":0.36191486377844057,"score_spread":0.28988623495458365,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W3091886723","genre_codex":"review","genre_gemma":"review","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"review","genre_consensus":"review","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.00009109641,0.9989207,0.000039353723,0.00018532218,0.000103388214,0.0000016015172,0.000008941622,0.0000026347102,0.0006471341],"genre_scores_gemma":[0.0009288827,0.9982242,0.00010449571,0.0002697861,0.00011979636,0.0000034562752,0.000017365697,9.334858e-7,0.0003310732],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.99987125,0.000030224675,0.000022129216,0.000026975684,0.000036946116,0.000012418113],"domain_scores_gemma":[0.9998111,0.00011697159,0.00002592831,0.000004530073,0.000028204351,0.000013226377],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0004713844,0.0004738559,0.00090736896,0.0012677998,0.0001639322,0.00062192784,0.00052025414,0.0006927876,0.0020107545],"category_scores_gemma":[0.0005980711,0.00012331,0.0003113799,0.0010705832,0.0003927145,0.0006668713,0.0004434283,0.001053082,0.000985434],"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":[0.0001501892,0.000033137116,0.000299278,0.02219222,0.00011110033,0.00022334461,0.00007802466,0.00014801085,0.0012406668,0.0063618957,0.021037513,0.9481246],"study_design_scores_gemma":[0.00004213332,0.00013383238,0.0024904215,0.013309632,0.00028597369,0.0031036362,0.00011573592,0.000086896405,0.0005779698,0.0046901517,0.9751448,0.00001880604],"about_ca_topic_score_codex":0.0010995787,"about_ca_topic_score_gemma":0.0025126357,"teacher_disagreement_score":0.0020107545,"about_ca_system_score_codex":0.00050265,"about_ca_system_score_gemma":0.0007812678,"threshold_uncertainty_score":0.006726682},"labels":[],"label_agreement":null},{"id":"W3126149304","doi":"10.1212/nxg.0000000000000557","title":"Genome-Wide Association Study Meta-Analysis for Parkinson Disease Motor Subtypes","year":2021,"lang":"en","type":"article","venue":"Neurology Genetics","topic":"Neurological disorders and treatments","field":"Medicine","cited_by":43,"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; National Institute of Environmental Health Sciences; National Institute of Neurological Disorders and Stroke; Medical Research Council; National Institutes of Health; Assistance publique-Hôpitaux de Paris; Fondation de France; National Cancer Institute; Landspítali Háskólasjúkrahús; Bundesministerium für Bildung und Forschung; University of Glasgow; Parkinson's UK; National Institute on Aging; National Institute for Health and Care Research; Multiple System Atrophy Coalition; Biogen; Huffington Foundation; Agence Nationale de la Recherche; Sol Goldman Charitable Trust; Canada First Research Excellence Fund; American Parkinson Disease Association; Consortium canadien en neurodégénérescence associée au vieillissement; Deutsche Forschungsgemeinschaft; McGill University; Demensförbundet; Center for Individualized Medicine, Mayo Clinic; H. Lundbeck A/S; Burroughs Wellcome Fund; Lewy Body Dementia Association; University College London; Wellcome Trust; University of Dundee; Helsingin Yliopisto; U.S. Department of Defense; Itä-Suomen Yliopisto; Little Family Foundation; Parkinson Vereniging; Michael J. Fox Foundation for Parkinson's Research; Mayo Clinic; U.S. Department of Health and Human Services; Helsingin ja Uudenmaan Sairaanhoitopiiri; EU Joint Programme – Neurodegenerative Disease Research","keywords":"Genome-wide association study; Confidence interval; Odds ratio; Logistic regression; Internal medicine; Disease; Genetic model; Meta-analysis; Medicine; Genetics; Biology; Genotype; Single-nucleotide polymorphism; Gene","score_opus":0.057225091655516626,"score_gpt":0.301017137276883,"score_spread":0.2437920456213664,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W3126149304","genre_codex":"review","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":null,"domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.28334957,0.66898936,0.020818176,0.0032066465,0.0023859348,0.0003882304,0.01622445,0.0010426185,0.003595069],"genre_scores_gemma":[0.9514665,0.03631784,0.0049517816,0.0011938392,0.0006361923,0.00043961048,0.00380291,0.0001668987,0.0010244154],"study_design_codex":"meta_analysis","study_design_gemma":"meta_analysis","domain_scores_codex":[0.99313414,0.0030379104,0.0010069076,0.0019887793,0.0004730523,0.0003591006],"domain_scores_gemma":[0.99165994,0.005449933,0.0008841298,0.0012403097,0.00054050825,0.00022523227],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.008097012,0.0024301233,0.005834299,0.0030827906,0.0009982326,0.0022182178,0.0016840076,0.001918065,0.004187156],"category_scores_gemma":[0.014380233,0.0010454925,0.032694496,0.0049955416,0.00045043303,0.0009829988,0.0013704142,0.0023829115,0.00037840824],"study_design_candidate":"meta_analysis","study_design_consensus":"meta_analysis","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0042486857,0.000028532444,0.11656979,0.0072801528,0.85831344,0.0003658466,0.000060068167,0.0017566299,0.0010648638,0.0002895559,0.0028170599,0.0072053857],"study_design_scores_gemma":[0.0010161798,0.00022089832,0.06013946,0.00078600785,0.9309375,0.000328022,0.00005752824,0.0026789194,0.00040954092,0.0009309205,0.0024593356,0.000035755886],"about_ca_topic_score_codex":0.011799307,"about_ca_topic_score_gemma":0.014821702,"teacher_disagreement_score":0.011799307,"about_ca_system_score_codex":0.0008216646,"about_ca_system_score_gemma":0.0013490468,"threshold_uncertainty_score":0.042821586},"labels":[],"label_agreement":null},{"id":"W3135637915","doi":"10.1212/nxg.0000000000000572","title":"Associations Between Variant Repeat Interruptions and Clinical Outcomes in Myotonic Dystrophy Type 1","year":2021,"lang":"en","type":"article","venue":"Neurology Genetics","topic":"Genetic Neurodegenerative Diseases","field":"Neuroscience","cited_by":22,"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":"Deutsche Gesellschaft für Muskelkranke; University of Aberdeen; Sarepta Therapeutics; GW Pharmaceuticals; Biogen; PTC Therapeutics; Sanofi; Alexion Pharmaceuticals; European Commission; Pfizer","keywords":"Myotonic dystrophy; Medicine; Genetics; Trinucleotide repeat expansion; Biology; Internal medicine; Gene; Allele","score_opus":0.08087133640048896,"score_gpt":0.3642204814991383,"score_spread":0.2833491450986494,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W3135637915","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9983333,0.0010582008,0.000054467226,0.000052741576,0.0000057923276,0.000014025731,0.00017360451,0.0000028664256,0.00030499126],"genre_scores_gemma":[0.9994773,0.00012503394,0.000066825705,0.000024800185,0.00001330046,0.000012979636,0.00018738444,7.2542974e-7,0.00009148166],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9995378,0.00018308253,0.000053531912,0.00010168255,0.000075044896,0.000048808157],"domain_scores_gemma":[0.99812955,0.00042113205,0.0011528617,0.00004842942,0.00007906945,0.0001689484],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00082525675,0.00024645973,0.00038826797,0.00023760514,0.00022724282,0.00025883698,0.00020680742,0.00042876802,0.0015326702],"category_scores_gemma":[0.0024282373,0.0000785677,0.0002793174,0.00035676942,0.00012886082,0.00015891781,0.00018381138,0.00036771467,0.00008614289],"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":[0.010530515,0.00046577156,0.97192883,0.00018639784,0.0005841357,0.00012904777,0.00007459061,0.00019918635,0.0013958331,0.000021379414,0.00023873456,0.014245516],"study_design_scores_gemma":[0.00017282277,0.0012112692,0.9979235,0.000021240934,0.00012246451,0.00017888274,0.000024360981,0.0001580121,0.000080290454,0.000016301497,0.00008819569,0.00000270286],"about_ca_topic_score_codex":0.0010728509,"about_ca_topic_score_gemma":0.0016900557,"teacher_disagreement_score":0.0015326702,"about_ca_system_score_codex":0.00022275443,"about_ca_system_score_gemma":0.000117066826,"threshold_uncertainty_score":0.0051273108},"labels":[],"label_agreement":null},{"id":"W3138210879","doi":"10.1212/nxg.0000000000000579","title":"Phenotypic Spectrum of Seizure Disorders in MBD5-Associated Neurodevelopmental Disorder","year":2021,"lang":"en","type":"article","venue":"Neurology Genetics","topic":"Genomics and Rare Diseases","field":"Biochemistry, Genetics and Molecular Biology","cited_by":18,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Montreal Children's Hospital","funders":"Eunice Kennedy Shriver National Institute of Child Health and Human Development; Medical Research Council; National Institute for Health and Care Research; McGill University Health Centre; National Health and Medical Research Council; McGill University","keywords":"Status epilepticus; Epilepsy; Pediatrics; Lennox–Gastaut syndrome; Myoclonic Jerk; Medicine; Intellectual disability; Seizure types; Psychology; Psychiatry","score_opus":0.0035572134586858545,"score_gpt":0.201913607296985,"score_spread":0.19835639383829914,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W3138210879","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9962599,0.00059827825,0.00040897453,0.000114837,0.0000070521164,0.000014907292,0.00020971001,0.000028918308,0.0023574687],"genre_scores_gemma":[0.9990716,0.0001750097,0.00031864812,0.000054918724,0.00001093138,0.000006610178,0.00015972654,0.0000052290216,0.00019725776],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9998355,0.000023967365,0.00002397834,0.00002971209,0.000036898706,0.000049875973],"domain_scores_gemma":[0.99979335,0.00005385107,0.0000633195,0.000006885256,0.000028193952,0.000054354907],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00012627731,0.00067535933,0.00025214296,0.00060805475,0.00032852413,0.00021931448,0.00019351848,0.00028277448,0.002365534],"category_scores_gemma":[0.00083909126,0.00008544308,0.00016345628,0.00028372047,0.00031590788,0.00016661893,0.00047005402,0.00021453254,0.00026722535],"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":[0.0003355786,0.00011109832,0.7384108,0.00012859,0.00006804712,0.19658528,0.00045997667,0.00061155035,0.025523951,0.0005501374,0.0017346562,0.03548044],"study_design_scores_gemma":[0.000034118984,0.00030118442,0.6104683,0.000057478162,0.000048368427,0.3833651,0.00035616936,0.00050703,0.0025367993,0.00031421974,0.0019989482,0.000012317521],"about_ca_topic_score_codex":0.00091506913,"about_ca_topic_score_gemma":0.0016526561,"teacher_disagreement_score":0.002365534,"about_ca_system_score_codex":0.00021140992,"about_ca_system_score_gemma":0.00018040759,"threshold_uncertainty_score":0.00791347},"labels":[],"label_agreement":null},{"id":"W3139400559","doi":"10.1212/nxg.0000000000000575","title":"Expanding the Spectrum of Movement Disorders Associated With <i>C9orf72</i> Hexanucleotide Expansions","year":2021,"lang":"en","type":"article","venue":"Neurology Genetics","topic":"Amyotrophic Lateral Sclerosis Research","field":"Medicine","cited_by":35,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Canadian Sport Centre Pacific","funders":"Wellcome Trust","keywords":"C9orf72; Parkinsonism; Amyotrophic lateral sclerosis; Movement disorders; Myoclonus; Medicine; Frontotemporal dementia; Dystonia; Chorea; Pediatrics; Retrospective cohort study; Internal medicine; Dementia; Disease; Psychiatry","score_opus":0.018978320243513473,"score_gpt":0.26968002293450566,"score_spread":0.2507017026909922,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W3139400559","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9980531,0.0006907066,0.00020389422,0.000043082713,0.0000049989094,0.000012716645,0.00013640439,0.000008431353,0.00084676425],"genre_scores_gemma":[0.9991891,0.000325594,0.00019270489,0.00004751303,0.00001756804,0.0000029371067,0.00015219198,0.0000026788148,0.00006973746],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.999705,0.000042063362,0.00005439153,0.00007523777,0.000052918764,0.00007040023],"domain_scores_gemma":[0.9992613,0.00018580149,0.00038472447,0.000035502082,0.000052820218,0.00007984115],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.000350645,0.0003032572,0.00021467231,0.0009941942,0.0002932856,0.00032370642,0.0001722344,0.0002948666,0.0015975443],"category_scores_gemma":[0.00091964036,0.0001459704,0.00026080685,0.0006855877,0.0003724786,0.00040465387,0.00038228426,0.00024963348,0.00026059707],"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":[0.00016210169,0.000031236847,0.97166055,0.000033319127,0.000022717682,0.014941436,0.00019258536,0.000047450692,0.0044199396,0.00006445974,0.00018151273,0.008242656],"study_design_scores_gemma":[0.000011713015,0.0001343463,0.9272747,0.00003941048,0.00003190359,0.07025245,0.00033108616,0.00013624672,0.0008870674,0.00011210397,0.00078001915,0.000009124297],"about_ca_topic_score_codex":0.001345148,"about_ca_topic_score_gemma":0.002067799,"teacher_disagreement_score":0.0015975443,"about_ca_system_score_codex":0.00013181931,"about_ca_system_score_gemma":0.00017266998,"threshold_uncertainty_score":0.0053443313},"labels":[],"label_agreement":null},{"id":"W3183702232","doi":"10.1212/nxg.0000000000000605","title":"Disease Severity and Motor Impairment Correlate With Health-Related Quality of Life in AP-4-Associated Hereditary Spastic Paraplegia","year":2021,"lang":"en","type":"article","venue":"Neurology Genetics","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":8,"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":"Studienstiftung des Deutschen Volkes; Astellas Pharma; Intellectual and Developmental Disabilities Research Center; Hospital for Sick Children; Deutsche Forschungsgemeinschaft; National Institutes of Health; University of Cambridge; National Institute of Neurological Disorders and Stroke; Quadrant Biosciences; Spastic Paraplegia Foundation; Celgene; Biogen","keywords":"Hereditary spastic paraplegia; Paraplegia; Disease; Medicine; Motor impairment; Spastic; Physical medicine and rehabilitation; Quality of life (healthcare); Pediatrics; Internal medicine; Cerebral palsy; Psychiatry; Spinal cord; Biology; Genetics","score_opus":0.03359141474154514,"score_gpt":0.2692310433531692,"score_spread":0.23563962861162407,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W3183702232","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9996369,0.00010200908,0.000038296297,0.000019014662,0.0000014640931,0.0000023441971,0.000048506907,0.0000012969203,0.00015029397],"genre_scores_gemma":[0.99982506,0.00002091825,0.000028994958,0.000006076966,0.0000026481594,0.000001902193,0.000083039195,3.3604243e-7,0.00003110948],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99969554,0.00010718366,0.000048324502,0.00004169139,0.000059670627,0.000047636317],"domain_scores_gemma":[0.99840254,0.00031421444,0.00082130765,0.00005910077,0.00013893867,0.00026392093],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0005915516,0.00027197797,0.00025811172,0.00071468053,0.00021809292,0.00039150417,0.00017489269,0.00034334976,0.0014764871],"category_scores_gemma":[0.00287509,0.00015605496,0.00035130745,0.00045147544,0.00034346056,0.0003124144,0.00052968215,0.00036147356,0.00015347691],"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":[0.000050544422,0.000013998917,0.99894613,0.000004420441,0.00003067297,0.00006981485,0.000035666984,0.000053356587,0.00016732994,0.0000042972633,0.000024236264,0.0005994328],"study_design_scores_gemma":[0.000002010237,0.00005522246,0.9994111,0.0000023299465,0.00000984266,0.0002869162,0.00004953391,0.000119829616,0.000030352561,0.000010681936,0.00002076817,0.0000014937104],"about_ca_topic_score_codex":0.0017638919,"about_ca_topic_score_gemma":0.0015882977,"teacher_disagreement_score":0.0017638919,"about_ca_system_score_codex":0.00018551014,"about_ca_system_score_gemma":0.00013112079,"threshold_uncertainty_score":0.0049393773},"labels":[],"label_agreement":null},{"id":"W3189485021","doi":"10.1212/nxg.0000000000000618","title":"Pathogenic <i>DNM1</i> Gene Variant Presenting With Unusually Nonsevere Neurodevelopmental Phenotype: A Case Report","year":2021,"lang":"en","type":"article","venue":"Neurology Genetics","topic":"Cellular transport and secretion","field":"Biochemistry, Genetics and Molecular Biology","cited_by":10,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"McMaster Children's Hospital","funders":"","keywords":"Intellectual disability; Epilepsy; Global developmental delay; Missense mutation; Neurology; Phenotype; Medicine; Hypotonia; Compound heterozygosity; Pediatrics; Genetic testing; Bioinformatics; Genetics; Psychiatry; Gene; Biology; Internal medicine","score_opus":0.008067303578740756,"score_gpt":0.20840696690384433,"score_spread":0.20033966332510358,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W3189485021","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9895182,0.0018560375,0.002436733,0.0011319872,0.00018611804,0.000100238016,0.00018453074,0.00014853434,0.004437504],"genre_scores_gemma":[0.9961182,0.0007459434,0.0014237224,0.0004272758,0.0003948045,0.00002379247,0.00007952711,0.000027468035,0.0007593016],"study_design_codex":"case_report","study_design_gemma":"case_report","domain_scores_codex":[0.9992501,0.000064402266,0.00008303198,0.00021838285,0.00009537683,0.00028860313],"domain_scores_gemma":[0.9989693,0.00025411113,0.0003022993,0.000112020694,0.000057112793,0.00030512735],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00032716358,0.001958888,0.0009257292,0.0018227797,0.002282663,0.0013985331,0.0009284079,0.0041199615,0.0019587558],"category_scores_gemma":[0.0018368197,0.0010936513,0.0010857267,0.0010640434,0.0016908498,0.001410104,0.0015847341,0.0021304383,0.0005982281],"study_design_candidate":"case_report","study_design_consensus":"case_report","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.000014829362,0.00001946385,0.004184995,0.00001334334,0.0000057251236,0.9938828,0.00010950051,0.000030850355,0.00086770154,0.00010300679,0.00017661054,0.000591175],"study_design_scores_gemma":[0.000004588097,0.000021384049,0.0018139253,0.0000054373504,0.000007766897,0.9972729,0.000060350452,0.000104113766,0.00033650396,0.00009328071,0.0002736469,0.000006001541],"about_ca_topic_score_codex":0.0024556853,"about_ca_topic_score_gemma":0.0026445403,"teacher_disagreement_score":0.0041199615,"about_ca_system_score_codex":0.0009415102,"about_ca_system_score_gemma":0.00065732875,"threshold_uncertainty_score":0.0068312287},"labels":[],"label_agreement":null},{"id":"W3205698253","doi":"10.1212/nxg.0000000000000631","title":"Expanding the Phenotypic Spectrum of GPI Anchoring Deficiency Due to Biallelic Variants in <i>GPAA1</i>","year":2021,"lang":"en","type":"article","venue":"Neurology Genetics","topic":"Trypanosoma species research and implications","field":"Medicine","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":"Centre Hospitalier Universitaire Sainte-Justine","funders":"","keywords":"Phenotype; Flow cytometry; Hypotonia; Neuroimaging; Clinical phenotype; Biology; Cytometry; Genetics; Pathology; Medicine; Neuroscience; Gene","score_opus":0.03177688101003051,"score_gpt":0.3075214115311666,"score_spread":0.27574453052113607,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W3205698253","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9962446,0.0003322801,0.00072514656,0.0002025373,0.000010539305,0.000017041164,0.00012317837,0.000036290778,0.0023083503],"genre_scores_gemma":[0.9987595,0.00016298101,0.00066436705,0.00008303705,0.000031648844,0.0000051674874,0.000094066745,0.000011153367,0.00018811834],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9997322,0.000052860076,0.000042302177,0.000070497685,0.00004240611,0.000059718022],"domain_scores_gemma":[0.999622,0.00015700753,0.00009139304,0.000025299429,0.000038744667,0.00006557994],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0003137585,0.0011438733,0.00024407778,0.0009937396,0.00034638238,0.0004368201,0.0003370291,0.00062814425,0.0024527642],"category_scores_gemma":[0.00090204005,0.0001698894,0.0002064404,0.0005103287,0.0005319618,0.00029021094,0.0006129911,0.0005017826,0.0004066518],"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":[0.00092255004,0.00021045777,0.42122883,0.00020624339,0.000104913284,0.35392207,0.0013944405,0.00053218554,0.17544994,0.0015634324,0.0019854077,0.042479444],"study_design_scores_gemma":[0.000052305513,0.0003743381,0.23206256,0.00006267348,0.00008810757,0.75389874,0.00037369088,0.0006685254,0.009146395,0.0007029108,0.002547444,0.000022286178],"about_ca_topic_score_codex":0.00057470263,"about_ca_topic_score_gemma":0.0007873763,"teacher_disagreement_score":0.0024527642,"about_ca_system_score_codex":0.00014520618,"about_ca_system_score_gemma":0.00015866359,"threshold_uncertainty_score":0.008205295},"labels":[],"label_agreement":null},{"id":"W3206439979","doi":"10.1212/nxg.0000000000000623","title":"Investigating Late-Onset Pompe Prevalence in Neuromuscular Medicine Academic Practices","year":2021,"lang":"en","type":"article","venue":"Neurology Genetics","topic":"Lysosomal Storage Disorders Research","field":"Medicine","cited_by":7,"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":"Sanofi","keywords":"Medicine; Weakness; Internal medicine; Muscle weakness; Creatine kinase; Pediatrics; Gastroenterology; Surgery","score_opus":0.0731027347369553,"score_gpt":0.378855299952382,"score_spread":0.3057525652154267,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W3206439979","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99940455,0.00014070103,0.000032554977,0.000030411153,0.0000014177887,0.000007064681,0.00011246886,0.000002261665,0.00026848924],"genre_scores_gemma":[0.9996463,0.00008399916,0.000081285456,0.000029627334,0.0000043122423,0.0000047997196,0.00008421494,6.750005e-7,0.000064830274],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9992687,0.00015241065,0.00008347162,0.00013103933,0.00020761976,0.00015669943],"domain_scores_gemma":[0.9972705,0.00030613627,0.0013531861,0.00006119566,0.00040645828,0.00060256163],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0006703179,0.00019560773,0.00023794519,0.0013708959,0.00074659864,0.0007306468,0.00056238234,0.00044710442,0.002041351],"category_scores_gemma":[0.0027826023,0.00018290801,0.00013917401,0.0011814293,0.0004038548,0.00040420858,0.0007023123,0.00034482163,0.00024150134],"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":[0.000009965738,0.00001090121,0.999203,0.000004384287,0.000002500859,0.00003550042,0.00010199165,0.0000033890747,0.00006320136,0.0000029155751,0.000026601065,0.000535737],"study_design_scores_gemma":[0.000001958144,0.00006888105,0.9985623,0.000009742919,0.000004877505,0.00034818557,0.000796379,0.000045490822,0.000046157256,0.0000035166213,0.00011121391,0.0000013504643],"about_ca_topic_score_codex":0.04394462,"about_ca_topic_score_gemma":0.055446938,"teacher_disagreement_score":0.04394462,"about_ca_system_score_codex":0.0009320243,"about_ca_system_score_gemma":0.0010904657,"threshold_uncertainty_score":0.08737767},"labels":[],"label_agreement":null},{"id":"W4200407202","doi":"10.1212/nxg.0000000000000650","title":"Multigene Panel Testing in a Large Cohort of Adults With Epilepsy","year":2021,"lang":"en","type":"article","venue":"Neurology Genetics","topic":"Genomics and Rare Diseases","field":"Biochemistry, Genetics and Molecular Biology","cited_by":59,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Alberta Children's Hospital; University of Calgary","funders":"Invitae","keywords":"Genetic testing; Epilepsy; Medicine; Pediatrics; Cohort; Medical diagnosis; Genetic diagnosis; Psychiatry; Internal medicine; Pathology; Genetics; Biology","score_opus":0.011011953473739318,"score_gpt":0.21996213798725125,"score_spread":0.20895018451351194,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4200407202","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9990227,0.00013113757,0.0001019854,0.000041689244,0.0000040392247,0.000012858317,0.0003698568,0.0000033052222,0.00031236265],"genre_scores_gemma":[0.9993697,0.00008628226,0.00013016346,0.00007405734,0.000009909395,0.000013291787,0.00024700002,0.000001597099,0.00006806482],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9993874,0.00018464947,0.000062198524,0.00018128053,0.00011177864,0.00007269289],"domain_scores_gemma":[0.9986412,0.00032470093,0.0006295011,0.00013028622,0.00012463053,0.00014965094],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00077805074,0.00021926533,0.00019366542,0.00048162494,0.0004706402,0.00041026832,0.00019652919,0.00040085864,0.0013062609],"category_scores_gemma":[0.0025001098,0.00022469407,0.00023091499,0.000658154,0.00019358381,0.000438988,0.00044714555,0.0003528318,0.00022819554],"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":[0.00003416594,0.000013547724,0.9987129,0.0000035139165,0.000013282457,0.00012349698,0.00005373663,0.000012944514,0.00012104609,0.0000075542707,0.00010456312,0.00079939276],"study_design_scores_gemma":[0.00000725796,0.000090664784,0.99799216,0.000006506831,0.000014593379,0.0012232068,0.00015016191,0.00017786719,0.0000595572,0.000024693365,0.00025011442,0.000003285551],"about_ca_topic_score_codex":0.0044532814,"about_ca_topic_score_gemma":0.0059643555,"teacher_disagreement_score":0.0044532814,"about_ca_system_score_codex":0.00022311835,"about_ca_system_score_gemma":0.0002459996,"threshold_uncertainty_score":0.008854687},"labels":[],"label_agreement":null},{"id":"W4210359797","doi":"10.1212/nxg.0000000000000657","title":"Therapy Trial Design in Vanishing White Matter","year":2022,"lang":"en","type":"review","venue":"Neurology Genetics","topic":"RNA regulation and disease","field":"Biochemistry, Genetics and Molecular Biology","cited_by":32,"is_retracted":false,"has_abstract":true,"route_ca_aff":false,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"","funders":"National Institute of Neurological Disorders and Stroke; National Institutes of Health; Amsterdam Neuroscience; Association Européenne contre les Leucodystrophies; National Center for Advancing Translational Sciences; Nederlandse Organisatie voor Wetenschappelijk Onderzoek; Ministero della Salute; Vrije Universiteit Amsterdam; Hersenstichting; Denali Therapeutics; ZonMw; bluebird bio; McGill University; McGill University Health Centre; Stichting Metakids; Biogen; Fonds de Recherche du Québec - Santé; BC Children's Hospital; Eli Lilly and Company","keywords":"Disease; Medicine; White matter; Leukodystrophy; Clinical trial; Pediatrics; Internal medicine; Magnetic resonance imaging","score_opus":0.06685039888778331,"score_gpt":0.3224467204340817,"score_spread":0.25559632154629836,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4210359797","genre_codex":"empirical","genre_gemma":"review","domain_codex":null,"domain_gemma":"methods","model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"review","genre_consensus":null,"domain_candidate":"methods","domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.3343946,0.1785351,0.06070856,0.09933548,0.046611227,0.11055686,0.017945088,0.0018883584,0.15002461],"genre_scores_gemma":[0.7138963,0.017497007,0.02900579,0.044442113,0.0056595523,0.15544747,0.005515852,0.00027470582,0.028261244],"study_design_codex":"randomized_trial","study_design_gemma":"not_applicable","domain_scores_codex":[0.99377126,0.00477475,0.00040450404,0.00049354276,0.0002005848,0.00035548944],"domain_scores_gemma":[0.99614257,0.0019337907,0.00059357146,0.00032621782,0.00033813601,0.00066574075],"candidate_categories":["metaresearch"],"consensus_categories":[],"category_scores_codex":[0.007603178,0.00071844115,0.002309407,0.0004407806,0.00047288934,0.0014312705,0.00076336646,0.0025845745,0.023840927],"category_scores_gemma":[0.009996993,0.00019634806,0.0026693437,0.0004247781,0.0006419993,0.0015480785,0.0010609177,0.0032132354,0.0024168992],"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":[0.5407676,0.003125424,0.0038550063,0.015535325,0.0072085317,0.00046811468,0.00032239762,0.003040118,0.00263801,0.017914066,0.04255038,0.36257505],"study_design_scores_gemma":[0.60502523,0.08726714,0.009548239,0.0064275367,0.005422136,0.00047429878,0.0002673051,0.006748301,0.0019498292,0.040110666,0.23662975,0.00012953086],"about_ca_topic_score_codex":0.00024317882,"about_ca_topic_score_gemma":0.0006300852,"teacher_disagreement_score":0.99239683,"about_ca_system_score_codex":0.000830278,"about_ca_system_score_gemma":0.0016346673,"threshold_uncertainty_score":0.07975584},"labels":[],"label_agreement":null},{"id":"W4285394094","doi":"10.1212/nxg.0000000000000678","title":"Questioning the Association of the <i>STMN2</i> Dinucleotide Repeat With Amyotrophic Lateral Sclerosis","year":2022,"lang":"en","type":"article","venue":"Neurology Genetics","topic":"Amyotrophic Lateral Sclerosis Research","field":"Medicine","cited_by":4,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Université du Québec à Montréal; Montreal Neurological Institute and Hospital","funders":"","keywords":"Amyotrophic lateral sclerosis; Genetics; Cohort; Biology; Gene; Genetic association; Genotype; Single-nucleotide polymorphism; Bioinformatics; Medicine; Internal medicine; Disease","score_opus":0.016239531428718538,"score_gpt":0.22939861025528618,"score_spread":0.21315907882656765,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4285394094","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9940665,0.0013909455,0.0011242584,0.0018574615,0.000109932625,0.000013130155,0.00028910983,0.000013176619,0.0011354624],"genre_scores_gemma":[0.99824107,0.00016176769,0.00031239435,0.00092641026,0.00013623947,0.000006919041,0.000082877195,0.000005314847,0.00012691965],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9986161,0.00047701676,0.00014348724,0.00045054028,0.00018015245,0.00013279034],"domain_scores_gemma":[0.99354845,0.003908423,0.0011936955,0.00057195907,0.00043353054,0.00034408373],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0033688836,0.00031174318,0.00030271237,0.00044289557,0.00042934026,0.0006725592,0.00093885005,0.0015919533,0.0018801786],"category_scores_gemma":[0.010939985,0.00011827325,0.0005241255,0.00043959185,0.0009668293,0.0005837768,0.00051111344,0.00079715747,0.00020420158],"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":[0.00083972997,0.00008533496,0.97594005,0.00011070898,0.0010898963,0.0014417158,0.00082958996,0.00023478456,0.008671523,0.000734085,0.0011690127,0.008853572],"study_design_scores_gemma":[0.00008781295,0.00048119112,0.97770464,0.00010648517,0.0005122605,0.0035406868,0.0016592665,0.0019319936,0.006573635,0.0039682565,0.00340099,0.000032861655],"about_ca_topic_score_codex":0.0044773677,"about_ca_topic_score_gemma":0.0028001508,"teacher_disagreement_score":0.0044773677,"about_ca_system_score_codex":0.00018172123,"about_ca_system_score_gemma":0.00030285385,"threshold_uncertainty_score":0.017816603},"labels":[],"label_agreement":null},{"id":"W4311079561","doi":"10.1212/nxg.0000000000200043","title":"Identification of Sex-Specific Genetic Variants Associated With Tau PET","year":2022,"lang":"en","type":"article","venue":"Neurology Genetics","topic":"Alzheimer's disease research and treatments","field":"Medicine","cited_by":7,"is_retracted":false,"has_abstract":true,"route_ca_aff":false,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"","funders":"National Institute of Biomedical Imaging and Bioengineering; Canadian Institutes of Health Research; National Institutes of Health; Genentech; IXICO; H. Lundbeck A/S; Servier; Eisai; National Institute of Neurological Disorders and Stroke; Northern California Institute for Research and Education; F. Hoffmann-La Roche; Biogen; BioClinica; U.S. Department of Defense; Meso Scale Diagnostics; Alzheimer's Disease Neuroimaging Initiative; Novartis Pharmaceuticals Corporation; Pfizer; Eli Lilly and Company; Bristol-Myers Squibb; National Institute on Aging; Alzheimer's Association; Foundation for the National Institutes of Health","keywords":"Apolipoprotein E; Population stratification; Genotyping; Population; Cognitive impairment; Neuroimaging; Disease; Alzheimer's Disease Neuroimaging Initiative; Genetics; Psychology; Medicine; Internal medicine; Biology; Genotype; Gene; Neuroscience; Single-nucleotide polymorphism","score_opus":0.024152346133094957,"score_gpt":0.28020058557612126,"score_spread":0.2560482394430263,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4311079561","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9982004,0.00027456804,0.0006011235,0.000027567907,0.000007343674,0.000011930274,0.00042520557,0.000007802539,0.00044402506],"genre_scores_gemma":[0.99885,0.00005245228,0.0004903554,0.000031337808,0.0000076224037,0.000015535918,0.0002751319,0.000008873221,0.00026862958],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99961495,0.00009051097,0.00003741384,0.00014073992,0.000052083058,0.00006426494],"domain_scores_gemma":[0.9993088,0.00019179763,0.00030124924,0.000088414694,0.000047356807,0.00006224133],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0005506153,0.00032269914,0.00032214646,0.00039922373,0.00027891638,0.00043208766,0.00025216027,0.00033747908,0.0027048783],"category_scores_gemma":[0.0013984472,0.00012853964,0.00059750734,0.00045610324,0.00022301881,0.000112581176,0.00022140457,0.00024081708,0.00022297415],"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":[0.0011748349,0.000036639784,0.9788043,0.000027042495,0.00028523657,0.0005822642,0.00023346207,0.0001018641,0.009811564,0.00009001451,0.00020086975,0.008651874],"study_design_scores_gemma":[0.00003278349,0.00014345675,0.99646807,0.000005346228,0.00010320374,0.0008883006,0.00009635833,0.0003766495,0.0013383013,0.0001385784,0.0004031754,0.000005755781],"about_ca_topic_score_codex":0.0021782035,"about_ca_topic_score_gemma":0.0030271744,"teacher_disagreement_score":0.0027048783,"about_ca_system_score_codex":0.000095225216,"about_ca_system_score_gemma":0.00017257436,"threshold_uncertainty_score":0.00904876},"labels":[],"label_agreement":null},{"id":"W4317606070","doi":"10.1212/nxg.0000000000200055","title":"Neuropathology-Independent Association Between <i>APOE</i> Genotype and Cognitive Decline Rate in the Normal Aging-Early Alzheimer Continuum","year":2023,"lang":"en","type":"article","venue":"Neurology Genetics","topic":"Dementia and Cognitive Impairment Research","field":"Medicine","cited_by":16,"is_retracted":false,"has_abstract":true,"route_ca_aff":false,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"","funders":"National Institute on Aging; National Institutes of Health; National Institute of Neurological Disorders and Stroke; York University","keywords":"Apolipoprotein E; Clinical Dementia Rating; Neuropathology; Dementia; Cognitive decline; Senile plaques; Psychology; Internal medicine; Alzheimer's disease; Allele; Cognition; Medicine; Disease; Psychiatry; Biology; Genetics","score_opus":0.025924695729640068,"score_gpt":0.3151293046130043,"score_spread":0.28920460888336424,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4317606070","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99954706,0.000047554353,0.00014776587,0.000010921729,0.0000013853016,0.0000029042997,0.00008919163,0.000004599635,0.0001484669],"genre_scores_gemma":[0.99964106,0.000014686602,0.000120463155,0.000010052175,0.0000028329785,0.0000027986118,0.000117410214,0.0000024257347,0.00008831825],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9997199,0.000094239396,0.000024991396,0.00008765525,0.00003297594,0.0000401896],"domain_scores_gemma":[0.9973537,0.000633376,0.0011980489,0.00038544933,0.00018447364,0.00024492963],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0011635243,0.00023912353,0.00017459944,0.00057820056,0.00027119237,0.00041666583,0.00029559815,0.00038286013,0.0012499463],"category_scores_gemma":[0.0022204006,0.00017819127,0.00047827285,0.00032899805,0.00030580602,0.0002857772,0.00029523592,0.00047780783,0.00020183728],"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":[0.00052527746,0.000049666414,0.99693334,0.0000036628403,0.00008157383,0.00004753914,0.000036819292,0.00009523749,0.0010819332,0.000023957997,0.000031874442,0.0010891721],"study_design_scores_gemma":[0.0000066097664,0.000094605486,0.99896455,0.0000016080523,0.000033476626,0.0001440318,0.00003284244,0.00044198296,0.00018740892,0.00005286298,0.000036743713,0.0000032805576],"about_ca_topic_score_codex":0.0037629942,"about_ca_topic_score_gemma":0.003206925,"teacher_disagreement_score":0.0037629942,"about_ca_system_score_codex":0.00014454102,"about_ca_system_score_gemma":0.00018456005,"threshold_uncertainty_score":0.007482171},"labels":[],"label_agreement":null},{"id":"W4318016607","doi":"10.1212/nxg.0000000000200048","title":"Novel Homozygous Variant in <i>COQ7</i> in Siblings With Hereditary Motor Neuropathy","year":2023,"lang":"en","type":"article","venue":"Neurology Genetics","topic":"Coenzyme Q10 studies and effects","field":"Biochemistry, Genetics and Molecular Biology","cited_by":13,"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 Ottawa","funders":"Genome Alberta; Canada Research Chairs; Genome British Columbia; Muscular Dystrophy Canada; Canadian Institutes of Health Research; Genome Canada; Ontario Genomics; Ontario Genomics Institute; University of Ottawa","keywords":"Exome sequencing; Muscle biopsy; Compound heterozygosity; Biology; Coenzyme Q10; Carnitine; Internal medicine; Methionine; Muscle atrophy; Hydroxylation; Atrophy; Amino acid; Endocrinology; Medicine; Pathology; Genetics; Biochemistry; Biopsy; Gene; Enzyme; Mutation","score_opus":0.007995975143190346,"score_gpt":0.2161066229760286,"score_spread":0.20811064783283825,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4318016607","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.995199,0.00028550866,0.001130152,0.000547374,0.000072063674,0.00005522137,0.0003566795,0.00008362762,0.0022703216],"genre_scores_gemma":[0.9984463,0.00009846413,0.0005062285,0.00018316448,0.00004061057,0.000010613914,0.00011006248,0.000017946963,0.00058661844],"study_design_codex":"case_report","study_design_gemma":"observational","domain_scores_codex":[0.999634,0.000035131703,0.000033890574,0.00015240037,0.00007517712,0.00006937341],"domain_scores_gemma":[0.9993993,0.00016855543,0.00012216621,0.000029176626,0.00006036671,0.00022041776],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0002270319,0.0018391405,0.00055791065,0.0007926675,0.0014679898,0.0004315011,0.0007707583,0.0022628824,0.0036465065],"category_scores_gemma":[0.0012293421,0.00054460997,0.0005586306,0.0007076278,0.0009396833,0.00042804726,0.00083916,0.0010378407,0.00063213595],"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":[0.00010786999,0.000091201684,0.031730708,0.00004177756,0.00003309229,0.95110834,0.00075364945,0.00013983544,0.013132705,0.00023479393,0.0005817066,0.002044379],"study_design_scores_gemma":[0.00004167302,0.00031768356,0.087403305,0.000042313895,0.00006969194,0.90481347,0.0004935338,0.00060273416,0.0040708114,0.0004471189,0.001654057,0.000043593594],"about_ca_topic_score_codex":0.0040626433,"about_ca_topic_score_gemma":0.0037482402,"teacher_disagreement_score":0.0040626433,"about_ca_system_score_codex":0.00056069717,"about_ca_system_score_gemma":0.00053241197,"threshold_uncertainty_score":0.012198746},"labels":[],"label_agreement":null},{"id":"W4324321295","doi":"10.1212/nxg.0000000000200063","title":"New-Onset Refractory Status Epilepticus Due to a Novel MT-TF Variant","year":2023,"lang":"en","type":"article","venue":"Neurology Genetics","topic":"Glycogen Storage Diseases and Myoclonus","field":"Medicine","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":"Centre for Movement Disorders","funders":"","keywords":"Status epilepticus; Myoclonic epilepsy; Epilepsy; Multiplex ligation-dependent probe amplification; Medicine; Mitochondrial disease; Pediatrics; Exome sequencing; Epilepsia partialis continua; Heteroplasmy; Myoclonus; Mitochondrial DNA; Bioinformatics; Genetics; Pathology; Biology; Mutation; Anesthesia; Psychiatry; Exon; Gene","score_opus":0.021304953429713006,"score_gpt":0.280858580189669,"score_spread":0.259553626759956,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4324321295","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99679595,0.00036188227,0.0006754909,0.0003869965,0.000034915953,0.000017154325,0.000099830264,0.000023971717,0.0016038402],"genre_scores_gemma":[0.998988,0.00010279416,0.00024829933,0.000113119524,0.000060701448,0.0000046815207,0.00006562315,0.000005133981,0.00041168535],"study_design_codex":"case_report","study_design_gemma":"case_report","domain_scores_codex":[0.9999225,0.000009477475,0.000012258568,0.000023909066,0.0000105383,0.00002134369],"domain_scores_gemma":[0.99977165,0.00007008069,0.0000642559,0.000011133251,0.000014417337,0.00006852776],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00009669911,0.00064973166,0.0002529344,0.00032378203,0.00047213113,0.00021785848,0.00019505198,0.0007947978,0.0017833752],"category_scores_gemma":[0.0006390437,0.00009703524,0.00021934729,0.00027708441,0.00039119748,0.00019206773,0.00024972134,0.00034524908,0.00029827535],"study_design_candidate":"case_report","study_design_consensus":"case_report","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00018391068,0.00007114753,0.03733614,0.000039486204,0.000018438017,0.9439074,0.00023885671,0.00015224615,0.013004595,0.00042493266,0.0005647479,0.004058034],"study_design_scores_gemma":[0.00003756244,0.00016643746,0.034444448,0.000016783557,0.000024980256,0.9603349,0.00010493937,0.00050476857,0.002955514,0.00031681272,0.0010835726,0.000009292765],"about_ca_topic_score_codex":0.00089673424,"about_ca_topic_score_gemma":0.0011612877,"teacher_disagreement_score":0.0017833752,"about_ca_system_score_codex":0.00030037572,"about_ca_system_score_gemma":0.00023109472,"threshold_uncertainty_score":0.005965948},"labels":[],"label_agreement":null},{"id":"W4383874862","doi":"10.1212/nxg.0000000000200085","title":"Ataxia and Diplopia","year":2023,"lang":"en","type":"article","venue":"Neurology Genetics","topic":"Mitochondrial Function and Pathology","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":"McGill University Health Centre","funders":"","keywords":"Diplopia; Ataxia; Medicine; Surgery","score_opus":0.014754455004987925,"score_gpt":0.2494817058496491,"score_spread":0.23472725084466117,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4383874862","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9214685,0.007850582,0.0043965406,0.0017198925,0.00029349263,0.00012950988,0.0009820327,0.001151815,0.06200753],"genre_scores_gemma":[0.990812,0.0009658487,0.0011649197,0.0009329224,0.000098200115,0.000014100893,0.0002640797,0.00005493272,0.005693059],"study_design_codex":"case_report","study_design_gemma":"case_report","domain_scores_codex":[0.99979883,0.0000146803495,0.000020562473,0.00006105844,0.000032119067,0.000072806855],"domain_scores_gemma":[0.9996848,0.000046026093,0.00012666869,0.000026674188,0.000036602094,0.00007927608],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00007885593,0.0007535259,0.0004558642,0.0004993208,0.0005386187,0.00053669314,0.00027546656,0.0009357437,0.0048632873],"category_scores_gemma":[0.00086448545,0.0001784686,0.00040992428,0.00038116597,0.0005113873,0.000395447,0.00043712955,0.00069950544,0.0015242107],"study_design_candidate":"case_report","study_design_consensus":"case_report","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00025666592,0.00009304266,0.07838766,0.000269421,0.000088350665,0.8480816,0.000376894,0.0003748781,0.02109413,0.0021459693,0.0049801394,0.043851294],"study_design_scores_gemma":[0.00001756564,0.00012793866,0.03663597,0.00005409798,0.000023722696,0.9557514,0.00009537553,0.0002169426,0.0021301382,0.00037129302,0.0045647053,0.000010805233],"about_ca_topic_score_codex":0.0036390333,"about_ca_topic_score_gemma":0.00419788,"teacher_disagreement_score":0.0048632873,"about_ca_system_score_codex":0.0006332799,"about_ca_system_score_gemma":0.00049042644,"threshold_uncertainty_score":0.016269326},"labels":[],"label_agreement":null},{"id":"W4386215819","doi":"10.1212/nxg.0000000000200094","title":"Frequency of GAA- <i>FGF14</i> Ataxia in a Large Cohort of Brazilian Patients With Unsolved Adult-Onset Cerebellar Ataxia","year":2023,"lang":"en","type":"article","venue":"Neurology Genetics","topic":"Genetic Neurodegenerative Diseases","field":"Neuroscience","cited_by":36,"is_retracted":false,"has_abstract":true,"route_ca_aff":false,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"","funders":"Canadian Institutes of Health Research; University College London Hospitals NHS Foundation Trust; Fundação de Amparo à Pesquisa do Estado de São Paulo; Guarantors of Brain; Fondazione Cariplo; Medical Research Council; Aeglea BioTherapeutics; Wellcome Trust","keywords":"Ataxia; Cohort; Medicine; Population; Pediatrics; Internal medicine; Psychiatry","score_opus":0.011346955063753557,"score_gpt":0.2395349991610086,"score_spread":0.22818804409725504,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4386215819","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99938595,0.0001009739,0.00004259741,0.000021027685,0.0000015756812,0.0000074606196,0.00012437781,0.0000026060031,0.00031331295],"genre_scores_gemma":[0.9994362,0.00015451029,0.000056860892,0.000026958163,0.0000038799817,0.000008598369,0.00020764681,0.000002605103,0.00010274098],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9997508,0.00004399186,0.00003108813,0.00008317172,0.00004396791,0.000046982746],"domain_scores_gemma":[0.9993593,0.000079367346,0.0002650116,0.0000872014,0.00010308885,0.00010606152],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0003460508,0.00034856953,0.00043810986,0.00085252523,0.0005413154,0.000549945,0.00032233662,0.00036537484,0.0016155312],"category_scores_gemma":[0.0020410984,0.00033452726,0.0003511645,0.00072547677,0.0004277725,0.00022827281,0.0004605572,0.00022873425,0.00028073456],"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":[0.00003798373,0.000013537717,0.9970867,0.000007811453,0.000028993498,0.00032815186,0.00034889666,0.000016294478,0.00081075047,0.000018266186,0.000069741414,0.0012329766],"study_design_scores_gemma":[0.000008110265,0.000058057965,0.99737394,0.000010310352,0.00003095878,0.0016511084,0.0003487352,0.000078975994,0.00008612983,0.000029634419,0.00031910816,0.000004898886],"about_ca_topic_score_codex":0.020309513,"about_ca_topic_score_gemma":0.021444948,"teacher_disagreement_score":0.020309513,"about_ca_system_score_codex":0.00034227126,"about_ca_system_score_gemma":0.00029779685,"threshold_uncertainty_score":0.040382564},"labels":[],"label_agreement":null},{"id":"W4386856301","doi":"10.1212/nxg.0000000000200088","title":"Biallelic <i>SOX8</i> Variants Associated With Novel Syndrome With Myopathy, Skeletal Deformities, Intellectual Disability, and Ovarian Dysfunction","year":2023,"lang":"en","type":"article","venue":"Neurology Genetics","topic":"Genomics and Rare Diseases","field":"Biochemistry, Genetics and Molecular Biology","cited_by":3,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"St Mary's Hospital Centre; Hospital for Sick Children; Ottawa Hospital; Children's Hospital of Eastern Ontario","funders":"Genome Alberta; Canada Research Chairs; Genome British Columbia; Muscular Dystrophy Canada; Canadian Institutes of Health Research; Genome Canada; Ontario Genomics; Ontario Genomics Institute; University of Ottawa","keywords":"Biology; Genetics; Short stature; Compound heterozygosity; Global developmental delay; Phenotype; Gene; Endocrinology","score_opus":0.009931913126183113,"score_gpt":0.2008996498345544,"score_spread":0.1909677367083713,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4386856301","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99639904,0.0003147719,0.0010337216,0.00019827326,0.000027648053,0.000030586885,0.000745414,0.000060929902,0.0011896004],"genre_scores_gemma":[0.99758065,0.0001407979,0.0011245772,0.000114033784,0.000037830752,0.000013377514,0.00029311798,0.0000247693,0.00067086896],"study_design_codex":"case_report","study_design_gemma":"observational","domain_scores_codex":[0.999785,0.000013658839,0.00002667709,0.00010290326,0.000041503583,0.00003026903],"domain_scores_gemma":[0.9996917,0.000077086355,0.00011376512,0.000017160772,0.000015010289,0.00008528094],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00011264829,0.001027105,0.00029759877,0.0007159567,0.0006881547,0.00034448356,0.00032738323,0.0009876488,0.0043396223],"category_scores_gemma":[0.000375978,0.00025138902,0.00043914223,0.000668897,0.0007088235,0.00017968997,0.00049241673,0.0005514935,0.00036210957],"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":[0.0010591645,0.00014610324,0.16611642,0.00022310976,0.00022841743,0.49645746,0.0011283245,0.0004524611,0.3198016,0.0012246545,0.001209511,0.011952682],"study_design_scores_gemma":[0.00013333595,0.0002974153,0.2733461,0.00007616609,0.0002052928,0.6940799,0.00046798584,0.0010954355,0.02451666,0.0007018014,0.0050355317,0.000044440676],"about_ca_topic_score_codex":0.001856982,"about_ca_topic_score_gemma":0.003378805,"teacher_disagreement_score":0.0043396223,"about_ca_system_score_codex":0.00024531054,"about_ca_system_score_gemma":0.0002562636,"threshold_uncertainty_score":0.014517546},"labels":[],"label_agreement":null},{"id":"W4388034912","doi":"10.1212/nxg.0000000000200103","title":"mTOR Pathway Somatic Pathogenic Variants in Focal Malformations of Cortical Development","year":2023,"lang":"en","type":"article","venue":"Neurology Genetics","topic":"Tuberous Sclerosis Complex Research","field":"Medicine","cited_by":12,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"McGill University Health Centre","funders":"Fonds de Recherche du Québec - Santé; Canadian Institutes of Health Research; McGill University Health Centre; McGill University","keywords":"Cortical dysplasia; Biology; Germline; Somatic cell; Deep sequencing; Tuberous sclerosis; PI3K/AKT/mTOR pathway; Germline mutation; splice; Polymicrogyria; Genetics; Cancer research; Gene; Pathology; Epilepsy; Mutation; Medicine; Genome; Signal transduction; Neuroscience","score_opus":0.06699376299262809,"score_gpt":0.30892078648222276,"score_spread":0.24192702348959466,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4388034912","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9952845,0.00082943565,0.001033585,0.00011770228,0.000009445506,0.000017437864,0.0003756678,0.000061790706,0.0022702545],"genre_scores_gemma":[0.99919504,0.00009813368,0.0005210869,0.000025437257,0.000007940165,0.0000022467289,0.00007131137,0.0000053875665,0.0000733328],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99979645,0.000024680467,0.000029718525,0.00006204645,0.000054945365,0.000032225795],"domain_scores_gemma":[0.99957544,0.00013558152,0.00015597093,0.000029388579,0.000054009604,0.00004966524],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00022811398,0.0006170263,0.00020004246,0.0010972656,0.00028470083,0.0003217944,0.0002679057,0.00056276086,0.0020668062],"category_scores_gemma":[0.00088751275,0.00012715453,0.00019640161,0.0005059791,0.0005805654,0.00015179474,0.00029256032,0.00025823628,0.00020451607],"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":[0.0011821988,0.00014297507,0.62211984,0.00032576482,0.0003836945,0.14110091,0.00043428698,0.0024185616,0.19087142,0.0014368524,0.0016975431,0.037885927],"study_design_scores_gemma":[0.000056622954,0.00024210908,0.5273559,0.000096932876,0.00026962403,0.4237506,0.0002386356,0.00246407,0.042277377,0.0013901418,0.001821605,0.000036430065],"about_ca_topic_score_codex":0.0013929317,"about_ca_topic_score_gemma":0.0022937427,"teacher_disagreement_score":0.0020668062,"about_ca_system_score_codex":0.0002450805,"about_ca_system_score_gemma":0.0002349393,"threshold_uncertainty_score":0.0069141984},"labels":[],"label_agreement":null},{"id":"W4388750229","doi":"10.1212/nxg.0000000000200105","title":"Adult Phenotype of <i>SYNGAP1</i> -DEE","year":2023,"lang":"fa","type":"article","venue":"Neurology Genetics","topic":"Genomics and Rare Diseases","field":"Biochemistry, Genetics and Molecular Biology","cited_by":15,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Toronto Western Hospital; Centre for Addiction and Mental Health; University Health Network","funders":"National Institute on Deafness and Other Communication Disorders; National Institute of Mental Health; National Institute on Aging; University Health Network Foundation; Centers for Disease Control and Prevention; Multidisciplinary University Research Initiative; National Institute of Neurological Disorders and Stroke; Novo Nordisk; International Rett Syndrome Foundation; Eisai; Novo Nordisk Fonden; Dravet Syndrome Foundation; National Science Foundation; GW Pharmaceuticals; University of Toronto","keywords":"Phenotype; Virology; Biology; Genetics; Gene","score_opus":0.008325052780055728,"score_gpt":0.23218946885117758,"score_spread":0.22386441607112184,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4388750229","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9982272,0.0001489895,0.00019516918,0.00003638527,0.000003717585,0.000009854984,0.0002501953,0.000007913734,0.0011206475],"genre_scores_gemma":[0.9992582,0.00007762386,0.0001856941,0.00004966615,0.000008643516,0.000004535221,0.00020634281,0.0000025643483,0.00020662461],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99990463,0.000010058009,0.000016651062,0.00002816562,0.0000135264545,0.00002702077],"domain_scores_gemma":[0.99957913,0.00007117365,0.00020202508,0.000018623326,0.000043760374,0.00008534732],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00014753386,0.00024872215,0.0001870645,0.00023258569,0.00027165015,0.0002280746,0.00012877925,0.00026157734,0.0026869539],"category_scores_gemma":[0.0005777472,0.000080423284,0.00013848115,0.00027435212,0.00026173252,0.00023298274,0.00026766036,0.00021939163,0.00033354165],"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":[0.00029851525,0.00007125567,0.9591866,0.00004260608,0.000022748933,0.023189198,0.00028510232,0.000085909036,0.00944643,0.00016263274,0.0004505168,0.006758503],"study_design_scores_gemma":[0.000016148937,0.00025506312,0.889929,0.000020588037,0.00001433031,0.10709991,0.00033754704,0.00014469527,0.0012958981,0.00011149984,0.0007690463,0.0000061504834],"about_ca_topic_score_codex":0.00082358776,"about_ca_topic_score_gemma":0.0010005082,"teacher_disagreement_score":0.0026869539,"about_ca_system_score_codex":0.00012573038,"about_ca_system_score_gemma":0.00011874777,"threshold_uncertainty_score":0.008988738},"labels":[],"label_agreement":null},{"id":"W4389469460","doi":"10.1212/nxg.0000000000200114","title":"Mitofusin 2 Variant Presenting With a Phenotype of Multiple System Atrophy of Cerebellar Subtype","year":2023,"lang":"en","type":"article","venue":"Neurology Genetics","topic":"Mitochondrial Function and Pathology","field":"Biochemistry, Genetics and Molecular Biology","cited_by":2,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"B.C. Women's Hospital & Health Centre; Canada's Michael Smith Genome Sciences Centre; Fraser Health; University of British Columbia","funders":"Michael Smith Health Research BC","keywords":"Cerebellar ataxia; Cerebellum; Pathology; Ataxia; Atrophy; Medicine; Neuroscience; Dysarthria; MFN2; Biology; Genetics; Audiology; Mitochondrial DNA","score_opus":0.011754598490796216,"score_gpt":0.21651820496989005,"score_spread":0.20476360647909383,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4389469460","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99774605,0.000233031,0.0003488884,0.00016638306,0.000019571024,0.00002182092,0.00012281966,0.000024086896,0.0013172615],"genre_scores_gemma":[0.9987709,0.00009442671,0.00030108477,0.000113335176,0.00006476758,0.0000071294794,0.00011229309,0.000008772254,0.00052720483],"study_design_codex":"case_report","study_design_gemma":"case_report","domain_scores_codex":[0.9998221,0.00000968369,0.000023280309,0.000069694644,0.00002509364,0.00005023155],"domain_scores_gemma":[0.999668,0.0000743372,0.00009586263,0.000018353794,0.000026592055,0.00011694548],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00013464695,0.0011682939,0.00047521878,0.0007419494,0.00084514474,0.00046303193,0.0004663159,0.0016564114,0.0030384187],"category_scores_gemma":[0.00088760786,0.0002754414,0.00033668548,0.0005053027,0.00047983803,0.0004481402,0.00044670058,0.0006851148,0.0004845527],"study_design_candidate":"case_report","study_design_consensus":"case_report","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00010087218,0.00009379967,0.062750936,0.000026241629,0.000022954087,0.92632824,0.00031979015,0.00010045266,0.008134865,0.00019778992,0.00026311283,0.0016608678],"study_design_scores_gemma":[0.000023138806,0.00016398085,0.05711981,0.0000095762125,0.000020420995,0.9409251,0.00014859941,0.00021680676,0.00082697504,0.00011209782,0.0004225975,0.000010908775],"about_ca_topic_score_codex":0.0018015871,"about_ca_topic_score_gemma":0.0026699658,"teacher_disagreement_score":0.0030384187,"about_ca_system_score_codex":0.00028815772,"about_ca_system_score_gemma":0.00036963014,"threshold_uncertainty_score":0.010164499},"labels":[],"label_agreement":null},{"id":"W4390569826","doi":"10.1212/nxg.0000000000200122","title":"Childhood-Onset Myopathy With Preserved Ambulation Caused by a Recurrent <i>ADSSL1</i> Missense Variant","year":2024,"lang":"en","type":"article","venue":"Neurology Genetics","topic":"Biochemical and Molecular Research","field":"Biochemistry, Genetics and Molecular Biology","cited_by":13,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Ottawa Hospital; Children's Hospital of Eastern Ontario; University of Ottawa","funders":"Canada Research Chairs; Canadian Institutes of Health Research; European Commission; Muscular Dystrophy Canada","keywords":"Myopathy; Medicine; Internal medicine; Weakness; Missense mutation; Muscle weakness; Hyporeflexia; Endocrinology; Gastroenterology; Pathology; Cardiology; Surgery; Biology; Genetics; Mutation; Gene","score_opus":0.008417877755017957,"score_gpt":0.24376916403817553,"score_spread":0.23535128628315757,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4390569826","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99725926,0.000089149544,0.00026866797,0.0000996873,0.000015483245,0.000016127009,0.00018721446,0.000041276286,0.002023121],"genre_scores_gemma":[0.9989065,0.000053795193,0.00034775696,0.000059550057,0.000020549727,0.000004638632,0.00012253443,0.000010150989,0.0004745393],"study_design_codex":"case_report","study_design_gemma":"case_report","domain_scores_codex":[0.99981564,0.00001439091,0.00001782135,0.000057664794,0.000028054037,0.00006649899],"domain_scores_gemma":[0.9996214,0.00006883458,0.00015399457,0.00001495993,0.000022504619,0.00011831938],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.000094665775,0.0011328101,0.0003121164,0.0005354972,0.0007713281,0.00027375587,0.0002912545,0.00047082483,0.003220604],"category_scores_gemma":[0.0004034929,0.00019765392,0.00031218873,0.00055385346,0.00090010226,0.00017278643,0.00044248143,0.0006842923,0.00037265138],"study_design_candidate":"case_report","study_design_consensus":"case_report","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0004469495,0.0002559154,0.29028007,0.00015027162,0.00010890962,0.63205665,0.0011901093,0.00065865257,0.06478068,0.0007056593,0.0015894196,0.007776657],"study_design_scores_gemma":[0.00006325735,0.00036201676,0.2957037,0.000029868494,0.000106185464,0.6922945,0.00054012024,0.0003345025,0.008699645,0.0001499051,0.0016881638,0.000028206896],"about_ca_topic_score_codex":0.0042111566,"about_ca_topic_score_gemma":0.005671946,"teacher_disagreement_score":0.0042111566,"about_ca_system_score_codex":0.00046854353,"about_ca_system_score_gemma":0.00056752854,"threshold_uncertainty_score":0.010774016},"labels":[],"label_agreement":null},{"id":"W4390717645","doi":"10.1212/nxg.0000000000200120","title":"Machine Learning Models of Polygenic Risk for Enhanced Prediction of Alzheimer Disease Endophenotypes","year":2024,"lang":"en","type":"article","venue":"Neurology Genetics","topic":"Genetic Associations and Epidemiology","field":"Biochemistry, Genetics and Molecular Biology","cited_by":16,"is_retracted":false,"has_abstract":true,"route_ca_aff":false,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"","funders":"National Institutes of Health; Genentech; IXICO; H. Lundbeck A/S; Servier; Eisai; Canadian Institutes of Health Research; GHR Foundation; Northern California Institute for Research and Education; Pfizer; Novartis Pharmaceuticals Corporation; Alzheimer's Disease Neuroimaging Initiative; Meso Scale Diagnostics; Avid Radiopharmaceuticals; Mayo Foundation for Medical Education and Research; Regeneron Pharmaceuticals; BioClinica; Mayo Clinic; Biogen; Bristol-Myers Squibb; Eli Lilly and Company","keywords":"Endophenotype; Dementia; Genome-wide association study; Neuroimaging; Disease; Medicine; Genetic architecture; Psychology; Internal medicine; Cognition; Biology; Single-nucleotide polymorphism; Genotype; Psychiatry; Quantitative trait locus; Genetics; Population","score_opus":0.02044579922958576,"score_gpt":0.25828017656472263,"score_spread":0.23783437733513688,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4390717645","genre_codex":"methods","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":null,"domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.49403754,0.0020709687,0.4964866,0.0022965318,0.00013948044,0.00012907093,0.0011387245,0.0015218088,0.0021792564],"genre_scores_gemma":[0.9471195,0.00022386319,0.04935556,0.00029134622,0.00010138727,0.00011221574,0.0008812708,0.000056495133,0.0018583874],"study_design_codex":"simulation_or_modeling","study_design_gemma":"simulation_or_modeling","domain_scores_codex":[0.99795747,0.0013703048,0.000086156964,0.00038677774,0.00011063892,0.00008871006],"domain_scores_gemma":[0.9919269,0.006639075,0.00047086776,0.0004544376,0.00040108146,0.00010758455],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0074909003,0.00075828226,0.00069680484,0.0009021926,0.00036306013,0.0008186646,0.00089059153,0.0006688426,0.0025430552],"category_scores_gemma":[0.013037439,0.00033789035,0.001436603,0.0006452952,0.00040209672,0.0009942831,0.00062632613,0.0012369066,0.0007758467],"study_design_candidate":"simulation_or_modeling","study_design_consensus":"simulation_or_modeling","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00080885517,0.00046245873,0.116609104,0.00023224001,0.0014453579,0.00021613628,0.00019650061,0.6701481,0.0024358965,0.0043582665,0.0042661494,0.19882095],"study_design_scores_gemma":[0.000023725455,0.00007022498,0.0092046205,0.00001893616,0.00005843672,0.000050161692,0.0000072643,0.98549044,0.00023985229,0.0044960706,0.0003295737,0.000010620522],"about_ca_topic_score_codex":0.0034711938,"about_ca_topic_score_gemma":0.004425301,"teacher_disagreement_score":0.0074909003,"about_ca_system_score_codex":0.00072777644,"about_ca_system_score_gemma":0.000714528,"threshold_uncertainty_score":0.039616168},"labels":[],"label_agreement":null},{"id":"W4391948913","doi":"10.1212/01.nxg.0001006556.49281.fb","title":"Proceedings of the 27th International Stroke Genetics Consortium Workshop","year":2024,"lang":"en","type":"article","venue":"Neurology Genetics","topic":"Cancer-related molecular mechanisms research","field":"Biochemistry, Genetics and Molecular Biology","cited_by":0,"is_retracted":false,"has_abstract":true,"route_ca_aff":false,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":true,"ca_institutions":"","funders":"","keywords":"Medicine; Library science; Computer science","score_opus":0.01113351389124924,"score_gpt":0.2755802206977046,"score_spread":0.2644467068064554,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4391948913","genre_codex":"other","genre_gemma":"other","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"other","genre_consensus":"other","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.013067243,0.036991812,0.005370318,0.24794826,0.32493532,0.0019992664,0.008356878,0.00106285,0.3602681],"genre_scores_gemma":[0.050108664,0.037627958,0.00811338,0.04740994,0.082123086,0.00504123,0.022709806,0.0016917615,0.7451742],"study_design_codex":"not_applicable","study_design_gemma":"not_applicable","domain_scores_codex":[0.9947567,0.0013826502,0.00030376067,0.000558106,0.0018834857,0.001115307],"domain_scores_gemma":[0.99282163,0.00055947807,0.00019795557,0.00022850434,0.0026870589,0.0035052593],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.010220099,0.0017548676,0.0009827431,0.0025367734,0.002664419,0.007699362,0.002341989,0.004109687,0.074884824],"category_scores_gemma":[0.0075509385,0.0004092137,0.0020482214,0.00169068,0.0009982783,0.0016859577,0.005650414,0.0047459607,0.029315637],"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":[0.00008533951,0.000058345086,0.00017416083,0.00011497614,0.000011199757,0.00030948405,0.0002857555,0.000080278,0.00018746397,0.0008855919,0.98065794,0.017149517],"study_design_scores_gemma":[0.000035942758,0.00003124739,0.0008168451,0.0003367091,0.000010701741,0.00014497868,0.0006740512,0.000047809895,0.00012379285,0.0007434743,0.99702007,0.000014369105],"about_ca_topic_score_codex":0.007938888,"about_ca_topic_score_gemma":0.014615279,"teacher_disagreement_score":0.074884824,"about_ca_system_score_codex":0.005852163,"about_ca_system_score_gemma":0.013009729,"threshold_uncertainty_score":0.25051475},"labels":[],"label_agreement":null},{"id":"W4399520750","doi":"10.1212/nxg.0000000000200165","title":"MRI Insights in Hypomyelinating Disorders With Early Myelination Disturbances","year":2024,"lang":"en","type":"article","venue":"Neurology Genetics","topic":"RNA regulation and disease","field":"Biochemistry, Genetics and Molecular Biology","cited_by":0,"is_retracted":false,"has_abstract":false,"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; Neuroscience; Anatomy; Physical medicine and rehabilitation; Radiology; Psychology","score_opus":0.004365797340882664,"score_gpt":0.22417431119594272,"score_spread":0.21980851385506006,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4399520750","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.93437403,0.028280944,0.012484955,0.0045414753,0.00019335102,0.000053348493,0.0005424551,0.000252506,0.019277027],"genre_scores_gemma":[0.980961,0.009475768,0.005719854,0.0004976281,0.00034364054,0.000018111683,0.0002138292,0.000037788945,0.0027322907],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.99992096,0.000017695627,0.000010737557,0.000014236285,0.000013483349,0.000022861548],"domain_scores_gemma":[0.99983263,0.00004421329,0.000050041635,0.000011933008,0.000026652726,0.000034408564],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00024055569,0.00066372805,0.00020945606,0.0019446282,0.00018629877,0.0004924426,0.00040249902,0.0009102035,0.002464636],"category_scores_gemma":[0.00044067408,0.0003422623,0.00018245462,0.00039096765,0.00055614376,0.0006383102,0.00033012283,0.0006000406,0.00043665417],"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":[0.0013167004,0.00013311995,0.019517781,0.0006207072,0.00012079085,0.11873912,0.0005279411,0.0008260585,0.808759,0.00797463,0.0021086007,0.039355576],"study_design_scores_gemma":[0.00019953102,0.00074750424,0.15163642,0.00035112048,0.00042665823,0.5063401,0.0013176283,0.0042825746,0.27658513,0.025853716,0.03217287,0.000086837754],"about_ca_topic_score_codex":0.0008874455,"about_ca_topic_score_gemma":0.0006016065,"teacher_disagreement_score":0.002464636,"about_ca_system_score_codex":0.00030470217,"about_ca_system_score_gemma":0.00016609517,"threshold_uncertainty_score":0.008244991},"labels":[],"label_agreement":null},{"id":"W4402670917","doi":"10.1212/nxg.0000000000200193","title":"Macrostructural Brain Abnormalities in Spinal Muscular Atrophy","year":2024,"lang":"en","type":"article","venue":"Neurology Genetics","topic":"Neurogenetic and Muscular Disorders Research","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":"Montreal Children's Hospital","funders":"","keywords":"Spinal muscular atrophy; Medicine; Physical medicine and rehabilitation; Neuroscience; Progressive muscular atrophy; Atrophy; Anatomy; Pathology; Psychology; Disease; Amyotrophic lateral sclerosis","score_opus":0.015444817617547872,"score_gpt":0.32409978498023795,"score_spread":0.3086549673626901,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4402670917","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9973846,0.0011370209,0.00024430084,0.00007117768,0.0000046992727,0.00000774406,0.0001263448,0.000013123011,0.0010109767],"genre_scores_gemma":[0.999102,0.0002959315,0.00030515567,0.000018670831,0.000010551928,0.000004384245,0.00009168553,0.0000023947898,0.00016927936],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99976605,0.00006054098,0.000024184,0.00005104245,0.00007805455,0.000020122585],"domain_scores_gemma":[0.99888486,0.00021031628,0.0006761535,0.000044384287,0.00011099242,0.00007340434],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00040955908,0.00035387505,0.0001682334,0.002114543,0.00021661179,0.00030688374,0.00021385512,0.00026838787,0.0023597078],"category_scores_gemma":[0.0016008333,0.00010129333,0.00010156115,0.00052288856,0.0004930663,0.00027397284,0.0004304026,0.00020500102,0.00020667868],"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":[0.00021479274,0.00003282623,0.9725045,0.00006397198,0.000095567004,0.0014795322,0.0001821301,0.0001904249,0.011280151,0.000114310795,0.00024461604,0.013597235],"study_design_scores_gemma":[0.0000012135953,0.000061996325,0.9953733,0.000013056865,0.0000143547595,0.0037017672,0.00005368109,0.00011227788,0.00046155826,0.00008944157,0.0001154794,0.0000019230592],"about_ca_topic_score_codex":0.0016187617,"about_ca_topic_score_gemma":0.0031502845,"teacher_disagreement_score":0.0023597078,"about_ca_system_score_codex":0.0001974663,"about_ca_system_score_gemma":0.00015164877,"threshold_uncertainty_score":0.007894039},"labels":[],"label_agreement":null},{"id":"W4403976350","doi":"10.1212/nxg.0000000000200208","title":"Bilateral Dentate Nuclei Hyperintensities and Response to 4-Aminopyridine in a Patient With Childhood-Onset GAA- <i>FGF14</i> -Related Ataxia","year":2024,"lang":"en","type":"article","venue":"Neurology Genetics","topic":"Fibroblast Growth Factor Research","field":"Biochemistry, Genetics and Molecular Biology","cited_by":4,"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":"McGill University","keywords":"Ataxia; Hyperintensity; Dentate nucleus; Neuroscience; 4-Aminopyridine; Medicine; Psychology; Internal medicine; Cerebellum; Magnetic resonance imaging","score_opus":0.005215272826624409,"score_gpt":0.22769932253667113,"score_spread":0.22248404971004673,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4403976350","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99736494,0.00037087422,0.00017817633,0.0002823126,0.000017327551,0.000026217922,0.00011465133,0.000027531913,0.0016179043],"genre_scores_gemma":[0.99916434,0.00015471947,0.00017621476,0.000098433884,0.000026533602,0.000004251259,0.00006361561,0.0000053712406,0.00030645155],"study_design_codex":"case_report","study_design_gemma":"case_report","domain_scores_codex":[0.9997904,0.000019062121,0.000026869906,0.000073860014,0.000029323024,0.000060554925],"domain_scores_gemma":[0.9995937,0.000097901146,0.00008869117,0.000018331788,0.000028920678,0.00017250996],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00015629159,0.0012509902,0.000616499,0.00096746883,0.0010389992,0.00044010382,0.00043607387,0.0016689968,0.0016702962],"category_scores_gemma":[0.00081798,0.00057316496,0.00038845194,0.0005400801,0.00084710034,0.0004627745,0.0004291731,0.0007669809,0.00035254363],"study_design_candidate":"case_report","study_design_consensus":"case_report","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00025014862,0.00009682878,0.059891652,0.000038541584,0.000028286644,0.9310159,0.00047791476,0.000095900046,0.006296985,0.00006649907,0.00026527178,0.0014759586],"study_design_scores_gemma":[0.00005382281,0.0002756904,0.109164484,0.000017262722,0.00005766673,0.8877387,0.0002606841,0.00025560055,0.001549669,0.00007297436,0.00053286995,0.000020516107],"about_ca_topic_score_codex":0.005668244,"about_ca_topic_score_gemma":0.008882905,"teacher_disagreement_score":0.005668244,"about_ca_system_score_codex":0.00086370454,"about_ca_system_score_gemma":0.0005188796,"threshold_uncertainty_score":0.011270523},"labels":[],"label_agreement":null},{"id":"W4404352190","doi":"10.1212/nxg.0000000000200206","title":"TRPM8 Mutations Associated With Persistent Pain After Surgical Injury of Corneal Trigeminal Axons","year":2024,"lang":"en","type":"article","venue":"Neurology Genetics","topic":"Ion Channels and Receptors","field":"Neuroscience","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":"National Center for Advancing Translational Sciences; Yale University; National Institutes of Health; Rehabilitation Research and Development Service; Paralyzed Veterans of America; Canadian Institutes of Health Research; U.S. Department of Veterans Affairs","keywords":"Medicine; Surgery; Anesthesia","score_opus":0.021564095810927865,"score_gpt":0.2565931212965377,"score_spread":0.23502902548560986,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4404352190","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9993375,0.00013504448,0.00026495705,0.000023394434,0.000005334311,0.000007525993,0.000059785252,0.000006945533,0.00015956607],"genre_scores_gemma":[0.9997329,0.00003799931,0.00010513121,0.000012647493,0.0000052981873,0.0000025541658,0.000042975254,0.000002437058,0.00005799765],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.99981254,0.000017446793,0.000030019237,0.00005317671,0.000044228687,0.000042594307],"domain_scores_gemma":[0.9996724,0.00007478022,0.00015616334,0.000016173204,0.000022902579,0.000057680954],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00009974819,0.00048096225,0.00026920566,0.00043544418,0.0003202079,0.0002757714,0.0002915176,0.0005580314,0.0012222554],"category_scores_gemma":[0.00047889623,0.00009655343,0.00036996117,0.0003921915,0.000443564,0.00016243767,0.0003603653,0.0003288472,0.00012969549],"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":[0.002558569,0.00031262363,0.21351163,0.00023685652,0.00022508117,0.13084252,0.0010777834,0.0006429978,0.6331587,0.0003237349,0.00033278024,0.016776785],"study_design_scores_gemma":[0.00011197786,0.0014930653,0.6422063,0.000049086997,0.0002674887,0.29390556,0.00081396126,0.002061576,0.057645086,0.0003113354,0.001086342,0.00004823094],"about_ca_topic_score_codex":0.000740064,"about_ca_topic_score_gemma":0.00074043934,"teacher_disagreement_score":0.0012222554,"about_ca_system_score_codex":0.00020855175,"about_ca_system_score_gemma":0.00011608947,"threshold_uncertainty_score":0.004088819},"labels":[],"label_agreement":null},{"id":"W4404559626","doi":"10.1212/nxg.0000000000200210","title":"Assessment of the Clinical Interactions of GAA Repeat Expansions in <i>FGF14</i> and <i>FXN</i>","year":2024,"lang":"en","type":"article","venue":"Neurology Genetics","topic":"Genetic Neurodegenerative Diseases","field":"Neuroscience","cited_by":4,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Montreal Neurological Institute and Hospital","funders":"National Institute of Neurological Disorders and Stroke; National Institutes of Health; Canadian Institutes of Health Research; Biogen; Friedreich's Ataxia Research Alliance","keywords":"Neuroscience; Biology","score_opus":0.05819541642043365,"score_gpt":0.39010520318510916,"score_spread":0.33190978676467553,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4404559626","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9987638,0.000111683854,0.00016333058,0.00003778899,0.000004992832,0.000008590397,0.000090243164,0.0000050721833,0.00081451586],"genre_scores_gemma":[0.99926084,0.000024523293,0.0003271226,0.00002478401,0.000007792516,0.000010209083,0.00010496098,0.000003264622,0.00023653255],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99948066,0.0001943115,0.00006171542,0.00011285468,0.00009238078,0.00005819508],"domain_scores_gemma":[0.9980901,0.00082402123,0.0005228004,0.00004674528,0.00019503929,0.0003212669],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0007413794,0.00037347432,0.00024469197,0.0007805017,0.0002545973,0.00028637887,0.00022908673,0.0005656926,0.002555843],"category_scores_gemma":[0.0022535718,0.00010005256,0.00026744432,0.00024611127,0.00025198003,0.00019451913,0.00021616017,0.0003623392,0.00025263193],"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":[0.0021548914,0.00022487462,0.92929393,0.000040185863,0.00020673178,0.0030967363,0.00020360982,0.00026183965,0.05525865,0.00006793142,0.00028049076,0.008910184],"study_design_scores_gemma":[0.000027664933,0.00092347624,0.98675925,0.000013763876,0.00010431948,0.0070807342,0.00013517361,0.0006456865,0.0038985952,0.00005816784,0.00034110656,0.000012079692],"about_ca_topic_score_codex":0.0011795368,"about_ca_topic_score_gemma":0.0021299254,"teacher_disagreement_score":0.002555843,"about_ca_system_score_codex":0.00031555453,"about_ca_system_score_gemma":0.00024379496,"threshold_uncertainty_score":0.008550167},"labels":[],"label_agreement":null},{"id":"W4404706166","doi":"10.1212/nxg.0000000000200194","title":"Adult Phenotype of <i>CHD2</i> -Associated Disorders","year":2024,"lang":"en","type":"article","venue":"Neurology Genetics","topic":"Genetics and Neurodevelopmental Disorders","field":"Biochemistry, Genetics and Molecular Biology","cited_by":4,"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":"University Health Network Foundation; Centers for Disease Control and Prevention; National Institute of Neurological Disorders and Stroke; National Institute of Mental Health; Multidisciplinary University Research Initiative; Novo Nordisk; Eisai; Dravet Syndrome Foundation; GW Pharmaceuticals; University of Toronto; National Science Foundation","keywords":"Phenotype; Biology; Genetics","score_opus":0.004488717427277319,"score_gpt":0.21463556135627326,"score_spread":0.21014684392899594,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4404706166","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.97783124,0.0020121066,0.0016078938,0.00048009044,0.00012030945,0.000103502374,0.008879037,0.00008634737,0.008879438],"genre_scores_gemma":[0.9924475,0.00044806456,0.001546439,0.00025279546,0.0001477527,0.000055441516,0.0036625513,0.000025965246,0.0014134499],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99965644,0.000048205882,0.000054816253,0.000117422656,0.000077141725,0.000045991794],"domain_scores_gemma":[0.99952054,0.00014094084,0.00019084779,0.000020930114,0.000060167396,0.0000665461],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00028886055,0.0010299206,0.00035129723,0.0009255418,0.00045836577,0.0004667484,0.000325573,0.000706452,0.0074435165],"category_scores_gemma":[0.0013415292,0.00010571306,0.00025569857,0.000969478,0.0003091552,0.00018498112,0.0003163066,0.00036847353,0.00057589717],"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":[0.0027895523,0.00017377193,0.88054776,0.00040071254,0.0004126282,0.030312369,0.0006043353,0.0006110868,0.037917256,0.0017496531,0.009010583,0.035470217],"study_design_scores_gemma":[0.00023672936,0.0003796483,0.9115946,0.00033268158,0.00053254666,0.0672545,0.00026906456,0.00075777463,0.0058003217,0.0009145032,0.011886186,0.000041402433],"about_ca_topic_score_codex":0.0026878256,"about_ca_topic_score_gemma":0.002866822,"teacher_disagreement_score":0.0074435165,"about_ca_system_score_codex":0.00019091526,"about_ca_system_score_gemma":0.00024234512,"threshold_uncertainty_score":0.024901032},"labels":[],"label_agreement":null},{"id":"W4405226126","doi":"10.1212/nxg.0000000000200201","title":"Shared Genetics of Migraine and Gastrointestinal Disorders Implicates Underlying Neurologic Mechanisms Yet Heterogeneous Etiologies","year":2024,"lang":"en","type":"article","venue":"Neurology Genetics","topic":"Migraine and Headache Studies","field":"Medicine","cited_by":4,"is_retracted":false,"has_abstract":true,"route_ca_aff":false,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"","funders":"National Institute of Neurological Disorders and Stroke; Norwegian Institute of Public Health; Medical Research Council; Terveyden ja hyvinvoinnin laitos; Institute of Genetics; Tartu Ülikool; Université de Bordeaux; Oulun Yliopisto; Rigshospitalet; Universitair Medisch Centrum Groningen; Samfundet Folkhälsan; Statens Serum Institut; University of Bristol; Landspítali Háskólasjúkrahús; University of Oxford; Vrije Universiteit Amsterdam; Rijksuniversiteit Groningen; Universität Ulm; Universiteit Leiden; Karolinska Institutet; Institut National de la Santé et de la Recherche Médicale; Erasmus Universitair Medisch Centrum Rotterdam; Helsingin ja Uudenmaan Sairaanhoitopiiri; King's College London; Broad Institute; Wellcome Trust; Ludwig-Maximilians-Universität München; Harvard T.H. Chan School of Public Health; Stanley Center for Psychiatric Research, Broad Institute; Novo Nordisk; Massachusetts General Hospital; Tampereen Yliopisto; QIMR Berghofer Medical Research Institute; Universitetet i Oslo; Helsingin Yliopisto; Brigham and Women's Hospital","keywords":"Etiology; Migraine; Familial hemiplegic migraine; Medicine; Genetics; Neuroscience; Bioinformatics; Biology; Pathology; Internal medicine; Migraine with aura","score_opus":0.044314939816023316,"score_gpt":0.3100464249584105,"score_spread":0.2657314851423872,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4405226126","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9922025,0.003825022,0.0015477362,0.00048388235,0.000019132014,0.00002357921,0.0004756371,0.000014006373,0.0014082994],"genre_scores_gemma":[0.9984485,0.0006032242,0.00054281304,0.000058265912,0.000029782288,0.000008287422,0.00020356906,0.0000025613272,0.00010298693],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99807286,0.0008060167,0.0001830389,0.00051006785,0.00026449581,0.00016353029],"domain_scores_gemma":[0.9963123,0.0014703406,0.0014580173,0.00039623966,0.00016911318,0.00019398781],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.001432731,0.00039714252,0.00053586275,0.0009838481,0.00038164412,0.0007724819,0.00039716196,0.0004708123,0.0023713186],"category_scores_gemma":[0.0043102284,0.00016748674,0.0007062837,0.0012969911,0.0009372083,0.0003699476,0.00068798783,0.00035729716,0.00013561283],"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":[0.00072435423,0.000061094,0.97098684,0.00021991855,0.0025145626,0.0012231729,0.0002807452,0.00028460933,0.008095272,0.0011665738,0.00023385306,0.014209035],"study_design_scores_gemma":[0.000033164975,0.00018044395,0.9948769,0.000041900636,0.0006284481,0.0019449625,0.00017064193,0.00022251807,0.00042931768,0.0010640556,0.00040165213,0.000005874709],"about_ca_topic_score_codex":0.002263075,"about_ca_topic_score_gemma":0.0025570493,"teacher_disagreement_score":0.0023713186,"about_ca_system_score_codex":0.0003376213,"about_ca_system_score_gemma":0.00058804074,"threshold_uncertainty_score":0.007932842},"labels":[],"label_agreement":null},{"id":"W4406312640","doi":"10.1212/nxg.0000000000200236","title":"Friedreich Ataxia","year":2025,"lang":"de","type":"article","venue":"Neurology Genetics","topic":"Genetic Neurodegenerative Diseases","field":"Neuroscience","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":"McGill University","funders":"","keywords":"Ataxia; Medicine; Physical medicine and rehabilitation; Psychiatry","score_opus":0.020922897337449103,"score_gpt":0.28390263584839603,"score_spread":0.2629797385109469,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4406312640","genre_codex":"other","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":null,"domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.03950866,0.22289045,0.023232812,0.011859313,0.006415711,0.0012163674,0.029727055,0.0066945655,0.6584551],"genre_scores_gemma":[0.2719895,0.10117769,0.019158674,0.019862264,0.0013255965,0.0010273376,0.05117067,0.00069204665,0.5335963],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.99929965,0.00006397767,0.00005516209,0.0002208471,0.00019406411,0.00016629668],"domain_scores_gemma":[0.99957925,0.00004191864,0.00006527837,0.000037287195,0.00019500086,0.00008132047],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0006009512,0.0019745803,0.0018372026,0.0017656755,0.0020851733,0.0028201833,0.001478623,0.0019970566,0.04027585],"category_scores_gemma":[0.0016176455,0.00024261375,0.00069382426,0.0018184702,0.0010540059,0.0016143234,0.002466692,0.0017596227,0.04380181],"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":[0.00052323355,0.0002722555,0.010896823,0.0017583973,0.00020599195,0.007611484,0.00054965506,0.0004007385,0.009298245,0.05346575,0.4514318,0.46358564],"study_design_scores_gemma":[0.00008618945,0.00011136461,0.0064383964,0.0007194215,0.000079359575,0.012292484,0.00012766432,0.00014482124,0.001705932,0.013907706,0.96433586,0.000050708768],"about_ca_topic_score_codex":0.009121697,"about_ca_topic_score_gemma":0.008810413,"teacher_disagreement_score":0.04027585,"about_ca_system_score_codex":0.002558211,"about_ca_system_score_gemma":0.0018908827,"threshold_uncertainty_score":0.13473612},"labels":[],"label_agreement":null},{"id":"W4406312686","doi":"10.1212/nxg.0000000000200232","title":"Neonatal Encephalopathy","year":2025,"lang":"en","type":"article","venue":"Neurology Genetics","topic":"Genomics and Rare Diseases","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":"Women and Children’s Health Research Institute; University of Toronto; SickKids Foundation; Hospital for Sick Children; Alberta Health Services; McMaster Children's Hospital; University of Alberta","funders":"National Heart, Lung, and Blood Institute; Uniwersytet Warszawski; International Society on Thrombosis and Haemostasis","keywords":"In silico; Gene; Encephalopathy; Pathogenicity; Biology; Copy-number variation; Genetic variants; Genetics; Medicine; Computational biology; Bioinformatics; Genome; Internal medicine; Genotype","score_opus":0.003484937414979425,"score_gpt":0.22674276679241617,"score_spread":0.22325782937743674,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4406312686","genre_codex":"other","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":null,"domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.3570807,0.09232615,0.029892672,0.019387102,0.004692156,0.00078432896,0.011013314,0.0021625452,0.482661],"genre_scores_gemma":[0.8693974,0.03103126,0.011130502,0.008765946,0.0010671116,0.00048600484,0.0073413416,0.00024252095,0.070538],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.9996915,0.00005866847,0.000042941603,0.00006133335,0.000063223386,0.00008231898],"domain_scores_gemma":[0.9996388,0.00007320636,0.00007480909,0.000036317313,0.000092031674,0.000084801664],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00027175972,0.00066972565,0.00050975184,0.00067985005,0.00062960706,0.0006046111,0.0004893475,0.0006655694,0.019468514],"category_scores_gemma":[0.0016425624,0.00010230912,0.00031731813,0.0006797334,0.0003580881,0.0005067898,0.0008774519,0.0008457304,0.00532857],"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":[0.00115061,0.00028723993,0.12370177,0.0024265372,0.00021693303,0.27240103,0.0010277838,0.0008816486,0.012968656,0.03116068,0.07109297,0.48268414],"study_design_scores_gemma":[0.00009160527,0.00030279584,0.06503197,0.0018973821,0.00015731523,0.5417494,0.0009509371,0.00080641505,0.009509593,0.017901208,0.3615357,0.00006567312],"about_ca_topic_score_codex":0.0023208682,"about_ca_topic_score_gemma":0.0015782613,"teacher_disagreement_score":0.019468514,"about_ca_system_score_codex":0.00074672035,"about_ca_system_score_gemma":0.0008750407,"threshold_uncertainty_score":0.065128684},"labels":[],"label_agreement":null},{"id":"W4407356032","doi":"10.1212/nxg.0000000000200233","title":"Women With Genetic Epilepsies","year":2025,"lang":"en","type":"review","venue":"Neurology Genetics","topic":"Genetics and Neurodevelopmental Disorders","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":false,"ca_institutions":"Hamilton Health Sciences; Ontario Brain Institute; McMaster University; University of Toronto","funders":"","keywords":"Epilepsy; Genetics; Biology; Evolutionary biology; Medicine; Neuroscience","score_opus":0.013165083158504768,"score_gpt":0.2555423984899422,"score_spread":0.24237731533143744,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4407356032","genre_codex":"review","genre_gemma":"review","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"review","genre_consensus":"review","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.00046203687,0.9884963,0.00016426826,0.00067935424,0.00036874137,0.00001248301,0.0001392078,0.00001765912,0.009659923],"genre_scores_gemma":[0.0073563643,0.9869191,0.000250142,0.0015001431,0.00036479908,0.000020378675,0.00028278003,0.0000089953055,0.0032973655],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.99976295,0.000059093152,0.000042812346,0.00004104145,0.00006138613,0.00003274395],"domain_scores_gemma":[0.9997342,0.00015804633,0.000047724734,0.000011086501,0.00003230258,0.0000166619],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00036904728,0.00059301336,0.00070415967,0.0014150167,0.0002472904,0.0005753932,0.0003202372,0.0006571321,0.011594405],"category_scores_gemma":[0.0011394368,0.00010970466,0.0005523536,0.0016296774,0.00032531391,0.0006749597,0.000565657,0.00067955855,0.0032240977],"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":[0.00009547017,0.000028372424,0.001685123,0.029393679,0.00021410536,0.0034900347,0.00031633367,0.00015294155,0.0013505529,0.008073535,0.089559086,0.8656409],"study_design_scores_gemma":[0.000027668813,0.000031835432,0.0022216304,0.012323002,0.00023007691,0.018712379,0.00016743944,0.000019834617,0.00026557536,0.0017203311,0.964266,0.000014190431],"about_ca_topic_score_codex":0.001943174,"about_ca_topic_score_gemma":0.0033688052,"teacher_disagreement_score":0.011594405,"about_ca_system_score_codex":0.00035664835,"about_ca_system_score_gemma":0.0010259756,"threshold_uncertainty_score":0.038787186},"labels":[],"label_agreement":null},{"id":"W4407567885","doi":"10.1212/nxg.0000000000200241","title":"Whole Genome Variable Number Tandem Repeat Analysis in Alzheimer Disease","year":2025,"lang":"en","type":"article","venue":"Neurology Genetics","topic":"Genetic Neurodegenerative Diseases","field":"Neuroscience","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":"National Institute of Neurological Disorders and Stroke; National Heart, Lung, and Blood Institute; National Institutes of Health; Karl-Franzens-Universität Graz; Österreichische Forschungsförderungsgesellschaft; National Institute on Aging; Medizinische Universität Graz; Oesterreichische Nationalbank; Case Western Reserve University; University of Toronto; Erasmus Medisch Centrum; Austrian Science Fund; ZonMw; European Commission; EU Joint Programme – Neurodegenerative Disease Research; Russian Foundation for Basic Research; National Institute on Deafness and Other Communication Disorders; University of Miami; National Human Genome Research Institute; Nederlandse Organisatie voor Wetenschappelijk Onderzoek; Vanderbilt University","keywords":"Variable number tandem repeat; Tandem repeat; Disease; Genome; Genetics; Biology; Computational biology; Tandem; Medicine; Gene; Pathology; Genotype","score_opus":0.02206429515181884,"score_gpt":0.28458428526579704,"score_spread":0.2625199901139782,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4407567885","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9906783,0.00229201,0.0041709165,0.00012384598,0.000023499226,0.000024987234,0.0011882639,0.000046250156,0.0014519198],"genre_scores_gemma":[0.9917543,0.0006371454,0.0061978577,0.00006602444,0.00001584618,0.0000180502,0.0008121916,0.00001160338,0.00048712883],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99968624,0.00013040128,0.0000273065,0.00008012627,0.000057154757,0.0000188135],"domain_scores_gemma":[0.99963975,0.00015532174,0.000097769145,0.0000340022,0.000039613333,0.000033680437],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00072679255,0.00020996475,0.0001875943,0.0010524231,0.00019739948,0.00029967434,0.00021308352,0.00031953945,0.0012130557],"category_scores_gemma":[0.0011083035,0.00007556871,0.00017093193,0.0006842108,0.00018324108,0.00013163466,0.00021360163,0.00021995003,0.0001553496],"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":[0.0011007758,0.0001415598,0.8659785,0.00022523286,0.0007611577,0.0012071638,0.00020207177,0.001558179,0.053169288,0.00048895617,0.001086477,0.074080735],"study_design_scores_gemma":[0.000031288047,0.00020227175,0.9841314,0.000041515643,0.0002110374,0.0035816121,0.00008978032,0.0019640275,0.006820601,0.0009513272,0.00196203,0.000013247346],"about_ca_topic_score_codex":0.0016261332,"about_ca_topic_score_gemma":0.0024704528,"teacher_disagreement_score":0.0016261332,"about_ca_system_score_codex":0.00012225383,"about_ca_system_score_gemma":0.00015532249,"threshold_uncertainty_score":0.004058063},"labels":[],"label_agreement":null},{"id":"W4407828098","doi":"10.1212/nxg.0000000000200246","title":"The Neurodegenerative Disease Knowledge Portal","year":2025,"lang":"en","type":"review","venue":"Neurology Genetics","topic":"Biomedical Text Mining and Ontologies","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":"McGill University; Montreal Neurological Institute and Hospital","funders":"National Human Genome Research Institute","keywords":"Disease; Medicine; Pathology","score_opus":0.02836067930000892,"score_gpt":0.34824866040668,"score_spread":0.3198879811066711,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4407828098","genre_codex":"dataset","genre_gemma":"review","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"review","genre_consensus":null,"domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.00648449,0.0068308976,0.11857994,0.010886468,0.0010434954,0.0010639107,0.6469012,0.10886596,0.09934367],"genre_scores_gemma":[0.029580193,0.0070481943,0.11372582,0.005302983,0.0005552763,0.00097233086,0.81695145,0.007956477,0.01790719],"study_design_codex":"not_applicable","study_design_gemma":"not_applicable","domain_scores_codex":[0.99800915,0.0004684938,0.00039267057,0.0003473344,0.0006199039,0.00016234949],"domain_scores_gemma":[0.99254614,0.002769998,0.0005107365,0.0018361611,0.0010814073,0.0012554179],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.004321755,0.0011711328,0.0014199094,0.0065823407,0.000976563,0.007121776,0.0030358082,0.002722572,0.052547738],"category_scores_gemma":[0.014346466,0.0006736953,0.0008823591,0.007952773,0.0005324051,0.0057440777,0.008243264,0.0025642128,0.0446976],"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":[0.0005534268,0.00017735793,0.003658186,0.0024387476,0.00012921117,0.001541604,0.0005973946,0.0012576322,0.002151671,0.026695164,0.77524686,0.18555275],"study_design_scores_gemma":[0.00015746144,0.00003924324,0.0018435982,0.0005082889,0.000036646183,0.00080510735,0.00019391802,0.0017771252,0.0011753689,0.030414667,0.9629899,0.00005857149],"about_ca_topic_score_codex":0.0031309952,"about_ca_topic_score_gemma":0.004412463,"teacher_disagreement_score":0.052547738,"about_ca_system_score_codex":0.0012898939,"about_ca_system_score_gemma":0.0036167726,"threshold_uncertainty_score":0.17578971},"labels":[],"label_agreement":null},{"id":"W4407829517","doi":"10.1212/nxg.0000000000200253","title":"Involvement of the Superior Cerebellar Peduncles in GAA- <i>FGF14</i> Ataxia","year":2025,"lang":"en","type":"article","venue":"Neurology Genetics","topic":"Genetic Neurodegenerative Diseases","field":"Neuroscience","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":"Centre Hospitalier de l’Université de Montréal; McGill University; Montreal Neurological Institute and Hospital","funders":"","keywords":"Ataxia; Neuroscience; Cerebellar ataxia; Psychology; Physical medicine and rehabilitation; Medicine","score_opus":0.02225132481505418,"score_gpt":0.26063048407596806,"score_spread":0.23837915926091388,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4407829517","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9990638,0.00022157312,0.0001432372,0.000017110293,0.0000021346632,0.000006067696,0.00013129825,0.000007961063,0.00040685944],"genre_scores_gemma":[0.9995227,0.00008760938,0.00013296568,0.000011644768,0.0000039570427,0.0000028662357,0.00012384311,0.000002810133,0.00011163737],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9997147,0.00003469654,0.000041463754,0.000093987765,0.0000721237,0.000043099244],"domain_scores_gemma":[0.99899405,0.00015904824,0.00052460376,0.0000675565,0.00015508854,0.00009971834],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0004362121,0.0003441702,0.00030188813,0.0009982237,0.00038269412,0.00039092088,0.00031899824,0.00031812084,0.0018908934],"category_scores_gemma":[0.0014191618,0.00014583963,0.00023736013,0.0005487501,0.00039178753,0.00022407791,0.0003649425,0.00020024703,0.0003651461],"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":[0.00013621317,0.000017651728,0.97813135,0.000043573647,0.000075795906,0.006496363,0.00023058703,0.000069570946,0.009924681,0.00003974837,0.00018726525,0.0046471795],"study_design_scores_gemma":[0.000010730276,0.00017581464,0.95403355,0.000024328952,0.00009675114,0.04118496,0.0001583374,0.00019856115,0.003379437,0.000038955157,0.0006917569,0.000006879575],"about_ca_topic_score_codex":0.0033461493,"about_ca_topic_score_gemma":0.0050720754,"teacher_disagreement_score":0.0033461493,"about_ca_system_score_codex":0.00018669816,"about_ca_system_score_gemma":0.00031581303,"threshold_uncertainty_score":0.006653309},"labels":[],"label_agreement":null},{"id":"W4407946625","doi":"10.1212/nxg.0000000000200251","title":"Association of <i>DMD</i> Gene Variant Classes With Motor Outcomes in a Drug Registration Clinical Trial Setting","year":2025,"lang":"en","type":"article","venue":"Neurology Genetics","topic":"Muscle Physiology and Disorders","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":"Carleton University","funders":"","keywords":"Duchenne muscular dystrophy; Dystrophin; Medicine; Clinical trial; Null allele; Biology; Gene; Bioinformatics; Genetics; Internal medicine; Allele","score_opus":0.010942074126574912,"score_gpt":0.29688917773828716,"score_spread":0.28594710361171227,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4407946625","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9931972,0.0019050351,0.0009157202,0.00040695004,0.00003117,0.0004325492,0.0011265103,0.000021364374,0.001963556],"genre_scores_gemma":[0.99823403,0.000104416555,0.00058495597,0.00020668998,0.000030290024,0.00025384343,0.0004314285,0.000007554228,0.00014676654],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.97657984,0.016709222,0.002579218,0.0020952062,0.0013782998,0.0006582662],"domain_scores_gemma":[0.96246666,0.01509293,0.018261164,0.0017425366,0.0012187195,0.0012179447],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.017443424,0.0002886059,0.00086762913,0.00049623835,0.00055206125,0.0015156535,0.00061447604,0.0008744098,0.0029638547],"category_scores_gemma":[0.026979348,0.00019013228,0.00097316585,0.0008918377,0.00068154646,0.0006137105,0.0006290834,0.0008188402,0.00035941097],"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":[0.13186002,0.0010654806,0.8351622,0.0007450842,0.0039573726,0.0002641176,0.00022455872,0.0005633735,0.003747952,0.0006304498,0.0016699099,0.02010948],"study_design_scores_gemma":[0.01303432,0.025026126,0.9458335,0.00023783825,0.0042719105,0.0012010286,0.00031123016,0.002744337,0.0026705093,0.0010081435,0.003585515,0.0000755057],"about_ca_topic_score_codex":0.00043221185,"about_ca_topic_score_gemma":0.000909513,"teacher_disagreement_score":0.017443424,"about_ca_system_score_codex":0.00053180486,"about_ca_system_score_gemma":0.0008299312,"threshold_uncertainty_score":0.092250705},"labels":[],"label_agreement":null},{"id":"W4410513590","doi":"10.1212/nxg.0000000000200267","title":"<i>PRRT</i> <i>2</i> -Related Epilepsy","year":2025,"lang":"he","type":"article","venue":"Neurology Genetics","topic":"Epilepsy research and treatment","field":"Medicine","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":"SickKids Foundation; Hospital for Sick Children; University of Toronto; McMaster University","funders":"","keywords":"Epilepsy; Medicine; Pediatrics; Copy-number variation; Epilepsy syndromes; Genetic testing; Psychiatry; Internal medicine; Genetics; Biology; Gene","score_opus":0.012031316940852087,"score_gpt":0.2959352682537412,"score_spread":0.28390395131288915,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4410513590","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.980754,0.0025107537,0.0008970507,0.00024472858,0.000025300269,0.00012221216,0.004652385,0.000043833836,0.010749723],"genre_scores_gemma":[0.9952212,0.00052412384,0.00048660563,0.00018227188,0.000038401035,0.000053170606,0.002543818,0.000023292647,0.0009270117],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9992735,0.00013278834,0.00017347976,0.0001952631,0.000115395575,0.000109611676],"domain_scores_gemma":[0.9987513,0.00009785074,0.00087032194,0.000075628035,0.00009719264,0.00010775618],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.000570875,0.00041775798,0.00037318465,0.0006381481,0.00032842957,0.0004210614,0.00036316502,0.0002746997,0.0063412706],"category_scores_gemma":[0.0011544307,0.00009770953,0.0002528469,0.0010061671,0.00041609272,0.00038230082,0.00045602804,0.00024045433,0.0012721894],"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":[0.00025600358,0.000045138517,0.984165,0.000113636335,0.00009522092,0.004740721,0.00014743338,0.000055554323,0.0016987176,0.00029322,0.0012404704,0.007148861],"study_design_scores_gemma":[0.00005055049,0.00029934486,0.9102675,0.00018474119,0.00011689379,0.07899031,0.00042182978,0.00013061753,0.0016231177,0.0003078825,0.0075924373,0.000014892009],"about_ca_topic_score_codex":0.0014007398,"about_ca_topic_score_gemma":0.001890107,"teacher_disagreement_score":0.0063412706,"about_ca_system_score_codex":0.0002522882,"about_ca_system_score_gemma":0.0004927414,"threshold_uncertainty_score":0.02121371},"labels":[],"label_agreement":null},{"id":"W4411934395","doi":"10.1212/nxg.0000000000200275","title":"Diagnostic Accuracy of Clinical Manifestations in Identifying People With Tuberous Sclerosis Complex","year":2025,"lang":"en","type":"article","venue":"Neurology Genetics","topic":"Tuberous Sclerosis Complex Research","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":"Centre Hospitalier Universitaire Sainte-Justine; Centre Hospitalier de l’Université de Montréal; Université de Montréal; Centre Hospitalier Universitaire de Sherbrooke; Université de Sherbrooke","funders":"","keywords":"Tuberous sclerosis; Medicine; Dermatology; Radiology","score_opus":0.15839940190886367,"score_gpt":0.4205909204880267,"score_spread":0.262191518579163,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4411934395","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99248934,0.0018932795,0.0017262262,0.00035457342,0.00004870542,0.000037864087,0.000927007,0.000052707233,0.002470317],"genre_scores_gemma":[0.99888283,0.0001245017,0.0006249837,0.0000329301,0.000017489596,0.000008035388,0.00027262175,0.0000031154398,0.00003347446],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99080443,0.0056641246,0.0009752502,0.0010350789,0.001119184,0.00040188618],"domain_scores_gemma":[0.9627643,0.02837343,0.004168369,0.0016991155,0.0021169935,0.0008778696],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.010261393,0.0007127278,0.0004961298,0.0034164933,0.00037633517,0.0015587957,0.001002424,0.0012230206,0.001005142],"category_scores_gemma":[0.056863412,0.00048099222,0.0009567874,0.001059428,0.00073135004,0.0011335339,0.0010710281,0.00085294864,0.00031538607],"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":[0.00018704751,0.000024438941,0.9948773,0.000025518144,0.00012451131,0.00005494736,0.000049162325,0.0005351879,0.00010441228,0.000041329877,0.00015379023,0.003822316],"study_design_scores_gemma":[0.00004638887,0.00022380833,0.98083204,0.00011311775,0.0004258374,0.0018945837,0.00023668737,0.014354768,0.0008559337,0.0005070212,0.00048448515,0.000025410081],"about_ca_topic_score_codex":0.0026144597,"about_ca_topic_score_gemma":0.0027977563,"teacher_disagreement_score":0.010261393,"about_ca_system_score_codex":0.00040097503,"about_ca_system_score_gemma":0.00045133688,"threshold_uncertainty_score":0.054268062},"labels":[],"label_agreement":null},{"id":"W4411984888","doi":"10.1212/nxg.0000000000200276","title":"Blood Biomarkers to Identify Renal Angiomyolipomas in People With Tuberous Sclerosis Complex","year":2025,"lang":"en","type":"article","venue":"Neurology Genetics","topic":"Tuberous Sclerosis Complex Research","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":"Western University; Université de Sherbrooke; Centre Hospitalier Universitaire Sainte-Justine; Centre Hospitalier Universitaire de Sherbrooke; Université de Montréal; Centre Hospitalier de l’Université de Montréal","funders":"","keywords":"Tuberous sclerosis; Medicine; Pathology; Angiomyolipoma; Kidney; Internal medicine","score_opus":0.045287195867700636,"score_gpt":0.32659396901419807,"score_spread":0.28130677314649744,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4411984888","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.98677176,0.006861625,0.0014692985,0.00077567936,0.00007894255,0.00008193975,0.0012793303,0.00012129466,0.0025601122],"genre_scores_gemma":[0.9974802,0.0005287913,0.0012031315,0.00019492459,0.000042679494,0.000026278782,0.0003080717,0.00000539727,0.00021049698],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9987344,0.00039733516,0.00016586788,0.00026766336,0.00030831966,0.00012643088],"domain_scores_gemma":[0.9960083,0.0011679877,0.0015859988,0.00016041027,0.0007880038,0.0002892365],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.002083742,0.000565235,0.00054705207,0.0024477167,0.00038670874,0.0010830454,0.0004597906,0.00081630977,0.00090441055],"category_scores_gemma":[0.007138648,0.0003070444,0.00052055623,0.0012637603,0.0002979383,0.0005671532,0.00058837066,0.00073449727,0.00027178694],"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":[0.0001225961,0.000028450148,0.99384636,0.000024240915,0.00008502163,0.000054877022,0.000042140608,0.00014824938,0.0003127304,0.000026593645,0.00036444416,0.004944206],"study_design_scores_gemma":[0.00004766445,0.00029751446,0.9915679,0.000102676844,0.00021513975,0.0010563246,0.00017220194,0.0032916053,0.001428281,0.00026491276,0.0015347438,0.000021036869],"about_ca_topic_score_codex":0.0038399785,"about_ca_topic_score_gemma":0.0041724113,"teacher_disagreement_score":0.0038399785,"about_ca_system_score_codex":0.00049243483,"about_ca_system_score_gemma":0.00045190944,"threshold_uncertainty_score":0.011020064},"labels":[],"label_agreement":null},{"id":"W4412532565","doi":"10.1212/nxg.0000000000200266","title":"Combating Genetic Heterogeneity for Polygenic Prediction of Susceptibility to Brain β-Amyloid Deposition","year":2025,"lang":"en","type":"article","venue":"Neurology Genetics","topic":"Bioinformatics and Genomic Networks","field":"Biochemistry, Genetics and Molecular Biology","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":"National Institutes of Health; Genentech; IXICO; H. Lundbeck A/S; Servier; Eisai; Canadian Institutes of Health Research; GHR Foundation; Northern California Institute for Research and Education; Pfizer; Novartis Pharmaceuticals Corporation; Mayo Foundation for Medical Education and Research; University of Southern California; Mayo Clinic; Biogen; Eli Lilly and Company; Bristol-Myers Squibb; BioClinica; Meso Scale Diagnostics; National Institute on Aging; Alzheimer's Association","keywords":"Deposition (geology); Genetic heterogeneity; Biology; Amyloid (mycology); Amyloid β; Genetics; Neuroscience; Medicine; Internal medicine; Pathology; Phenotype; Disease; Gene; Paleontology","score_opus":0.008841740035772585,"score_gpt":0.2521205977943381,"score_spread":0.2432788577585655,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4412532565","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9354202,0.0009781942,0.05793722,0.0023206854,0.00007415485,0.00007360606,0.001043628,0.00026598404,0.0018862939],"genre_scores_gemma":[0.98440325,0.00023731093,0.014295858,0.00012235844,0.00006985431,0.000032469536,0.00054462475,0.000026818003,0.00026750506],"study_design_codex":"observational","study_design_gemma":"simulation_or_modeling","domain_scores_codex":[0.997445,0.0016326284,0.00009644195,0.00054010004,0.000139383,0.00014650518],"domain_scores_gemma":[0.9924131,0.005422208,0.0008030457,0.0006915811,0.00024932632,0.00042077407],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.004274014,0.0006542653,0.00062269054,0.0023649153,0.0006319616,0.0012902219,0.0006574929,0.00057319936,0.0021771342],"category_scores_gemma":[0.013371067,0.00028702724,0.0010968858,0.0023400022,0.0005333236,0.0007506505,0.0010274579,0.0008280223,0.0003733921],"study_design_candidate":"simulation_or_modeling","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00044678015,0.00012978903,0.9280772,0.00007924542,0.0018336257,0.0006239202,0.00025414556,0.010344186,0.0040587843,0.0040665097,0.0013634521,0.048722293],"study_design_scores_gemma":[0.0001241804,0.00033250914,0.680051,0.000110209905,0.0022168893,0.0011285451,0.0004181156,0.2761782,0.0017625499,0.034430165,0.0031920832,0.000055543744],"about_ca_topic_score_codex":0.0061073317,"about_ca_topic_score_gemma":0.00919713,"teacher_disagreement_score":0.0061073317,"about_ca_system_score_codex":0.00039246958,"about_ca_system_score_gemma":0.0010427431,"threshold_uncertainty_score":0.022603393},"labels":[],"label_agreement":null},{"id":"W4412532658","doi":"10.1212/nxg.0000000000200248","title":"Executive Function Deficits in Genetic Frontotemporal Dementia","year":2025,"lang":"en","type":"article","venue":"Neurology Genetics","topic":"Amyotrophic Lateral Sclerosis 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":"McGill University; Douglas Mental Health University Institute; Western University; Sunnybrook Health Science Centre; Montreal Neurological Institute and Hospital; Occupational Cancer Research Centre; Université Laval","funders":"Medical Research Council; UK Dementia Research Institute; EU Joint Programme – Neurodegenerative Disease Research; National Institute for Health and Care Research; Brain Research UK; University College London; NIHR Cambridge Biomedical Research Centre; Wellcome Trust","keywords":"Frontotemporal dementia; Neuroscience; Executive functions; Psychology; Function (biology); Dementia; Physical medicine and rehabilitation; Cognitive psychology; Medicine; Cognition; Genetics; Biology; Internal medicine; Disease","score_opus":0.01959816830241734,"score_gpt":0.2879154646189674,"score_spread":0.26831729631655005,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4412532658","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99923456,0.00023760519,0.000030258912,0.000024800098,0.0000029035414,0.0000028869085,0.00007141505,0.000003376316,0.00039220843],"genre_scores_gemma":[0.9996245,0.00007972223,0.000055551525,0.000017144272,0.000004769527,0.000003158381,0.000115036084,8.0910047e-7,0.00009921819],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9998772,0.000029865036,0.000016010394,0.00002691733,0.0000337914,0.000016273023],"domain_scores_gemma":[0.99954295,0.00015485252,0.00018447313,0.000019728092,0.000045433477,0.000052704712],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00052733463,0.0007287581,0.0002751718,0.0010968246,0.0002979292,0.00033756692,0.00016792184,0.0003379232,0.0013252571],"category_scores_gemma":[0.0019585814,0.00010564796,0.000143364,0.00034192833,0.00035389222,0.00019351389,0.00026188802,0.0002441732,0.00013744897],"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":[0.001381063,0.0003200987,0.97160393,0.00006576865,0.00014726176,0.0033039756,0.0004824005,0.00036328586,0.0032795458,0.00014598735,0.0003867536,0.018519914],"study_design_scores_gemma":[0.000026670856,0.00023094086,0.99633265,0.0000145515605,0.00003926625,0.0024552858,0.00009232214,0.00018038636,0.0002455651,0.00026273157,0.000115497474,0.000004172497],"about_ca_topic_score_codex":0.0037284864,"about_ca_topic_score_gemma":0.004677081,"teacher_disagreement_score":0.0037284864,"about_ca_system_score_codex":0.00039056328,"about_ca_system_score_gemma":0.00020967989,"threshold_uncertainty_score":0.007413566},"labels":[],"label_agreement":null},{"id":"W4415484294","doi":"10.1212/nxg.0000000000200313","title":"Developing a National Network for Leukodystrophy Research and Care in Canada","year":2025,"lang":"en","type":"article","venue":"Neurology Genetics","topic":"Neutrophil, Myeloperoxidase and Oxidative Mechanisms","field":"Immunology and Microbiology","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":"Montreal Children's Hospital; Oakville-Trafalgar Memorial Hospital; Child and Family Research Institute; London Health Sciences Centre; Western University; McGill University; McGill University Health Centre; Children's Hospital of Western Ontario; Montreal Neurological Institute and Hospital","funders":"","keywords":"Excellence; Leukodystrophy; White paper; Multidisciplinary approach; Center of excellence; Disease; Translational research","score_opus":0.043522040774416834,"score_gpt":0.3053174441484925,"score_spread":0.26179540337407564,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4415484294","genre_codex":"commentary","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":null,"domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.054189127,0.05789737,0.023900717,0.581146,0.010129161,0.007792999,0.043895036,0.0026412487,0.21840839],"genre_scores_gemma":[0.44977343,0.06807213,0.16441593,0.16624507,0.0024151877,0.007609059,0.038985148,0.0008901573,0.1015939],"study_design_codex":"not_applicable","study_design_gemma":"not_applicable","domain_scores_codex":[0.9867072,0.002968319,0.0006701875,0.0008935617,0.005341446,0.0034192295],"domain_scores_gemma":[0.90058905,0.0033496616,0.0027178149,0.0013551445,0.060208153,0.031780113],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.015817774,0.0007022434,0.0008524017,0.004839387,0.009275644,0.0050185085,0.0038100753,0.0019422402,0.013033212],"category_scores_gemma":[0.027896522,0.00057925883,0.0011208337,0.004979285,0.0020388598,0.0016626014,0.006330274,0.003198987,0.0017204382],"study_design_candidate":"not_applicable","study_design_consensus":"not_applicable","about_ca_topic_candidate":true,"about_ca_topic_consensus":true,"about_ca_system_candidate":true,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00028340437,0.00023274987,0.06822375,0.0017735838,0.00025801666,0.00079992024,0.0023365393,0.0011449043,0.0011984853,0.03151233,0.6930294,0.19920693],"study_design_scores_gemma":[0.0003108839,0.0002029414,0.09050576,0.004905911,0.0002708502,0.0004738515,0.0046569724,0.0023203527,0.0006183107,0.0050468277,0.8904962,0.00019111838],"about_ca_topic_score_codex":0.98488706,"about_ca_topic_score_gemma":0.9901328,"teacher_disagreement_score":0.8643225,"about_ca_system_score_codex":0.1356775,"about_ca_system_score_gemma":0.5999195,"threshold_uncertainty_score":0.9844138},"labels":[],"label_agreement":null},{"id":"W4416014799","doi":"10.1212/nxg.0000000000200327","title":"Parkinson Disease <i>SNCA</i> Risk Variants Are Associated With Higher Asymmetric Putamen Dopaminergic Dysfunction","year":2025,"lang":"en","type":"article","venue":"Neurology Genetics","topic":"Parkinson's Disease Mechanisms and Treatments","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":"McGill University; McGill Genome Centre","funders":"","keywords":"Endophenotype; Putamen; Disease; Dopaminergic; Neuroimaging; Biomarker","score_opus":0.010204997513410823,"score_gpt":0.2296699840939714,"score_spread":0.21946498658056057,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4416014799","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9849569,0.0020740728,0.0018125554,0.001140212,0.00019821408,0.000041308936,0.0029432015,0.00010654208,0.0067270594],"genre_scores_gemma":[0.9967012,0.00025919947,0.0007213897,0.00016287052,0.000082817016,0.000012673625,0.00069047726,0.000030135689,0.0013392082],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99955064,0.000080575206,0.00006421792,0.00017029117,0.000088633846,0.00004564511],"domain_scores_gemma":[0.99904054,0.00024349916,0.00047947947,0.00006883409,0.00007852798,0.00008917313],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0003863642,0.0011163317,0.00043542983,0.000636398,0.0006104015,0.00079436816,0.00045883286,0.0013653127,0.011789015],"category_scores_gemma":[0.0019341487,0.00023385872,0.0009004621,0.00067561324,0.00037393713,0.00038096748,0.00038416646,0.0008896637,0.00072062964],"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":[0.00425585,0.0003042792,0.8731385,0.00035095145,0.0026110127,0.011155438,0.00053314783,0.0009841607,0.064389326,0.0024109443,0.0060531017,0.033813342],"study_design_scores_gemma":[0.000113967115,0.0002576109,0.97173756,0.00016720893,0.0011716925,0.014195434,0.00016200141,0.0012970296,0.0048327087,0.0020778424,0.003945964,0.000041035593],"about_ca_topic_score_codex":0.006691678,"about_ca_topic_score_gemma":0.00774976,"teacher_disagreement_score":0.011789015,"about_ca_system_score_codex":0.00031791284,"about_ca_system_score_gemma":0.00035899782,"threshold_uncertainty_score":0.039438188},"labels":[],"label_agreement":null},{"id":"W4417458373","doi":"10.1212/nxg.0000000000200334","title":"<i>DEGS1</i> -Related Hypomyelinating Leukodystrophy","year":2025,"lang":"en","type":"article","venue":"Neurology Genetics","topic":"RNA regulation and disease","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":"McMaster Children's Hospital; McMaster University; McMaster University Medical Centre","funders":"","keywords":"Leukodystrophy; Natural history; Phenotype; Stroke (engine); Clinical phenotype","score_opus":0.004711579153740887,"score_gpt":0.23574441403992755,"score_spread":0.23103283488618667,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4417458373","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99387556,0.0003971814,0.0009370309,0.00033056687,0.000033918648,0.000048297483,0.00055480935,0.00006850213,0.0037540887],"genre_scores_gemma":[0.9973066,0.00011531812,0.0008202046,0.00016564544,0.000023752054,0.000012399793,0.00039497777,0.000018256333,0.0011428657],"study_design_codex":"case_report","study_design_gemma":"case_report","domain_scores_codex":[0.9998294,0.000018772156,0.00002675767,0.000056056993,0.00002802589,0.000041006075],"domain_scores_gemma":[0.99978524,0.000052662162,0.00007156435,0.000014761463,0.00002128099,0.000054550866],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00022661472,0.0011655594,0.00028450222,0.00066755206,0.0005936872,0.00033482016,0.00030000223,0.0006332896,0.004098199],"category_scores_gemma":[0.00045296756,0.0001224454,0.00031687797,0.0003846975,0.0004786863,0.0001476404,0.00032588228,0.0004905283,0.0005037515],"study_design_candidate":"case_report","study_design_consensus":"case_report","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0017913776,0.00034428807,0.20977929,0.00036096878,0.00020555714,0.39996955,0.0012736188,0.001143378,0.35004395,0.002246248,0.003192995,0.02964875],"study_design_scores_gemma":[0.00011240969,0.00055473094,0.27182624,0.000118638316,0.00021050303,0.66427064,0.00044004805,0.0009775995,0.050513573,0.0008574663,0.010087892,0.000030295196],"about_ca_topic_score_codex":0.0011385016,"about_ca_topic_score_gemma":0.0015124392,"teacher_disagreement_score":0.004098199,"about_ca_system_score_codex":0.00044430964,"about_ca_system_score_gemma":0.0002905484,"threshold_uncertainty_score":0.013709843},"labels":[],"label_agreement":null},{"id":"W7116838294","doi":"10.1212/nxg.0000000000200339","title":"Pediatric Cohort of Charcot-Marie-Tooth Disease","year":2025,"lang":"en","type":"article","venue":"Neurology Genetics","topic":"Hereditary Neurological Disorders","field":"Neuroscience","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":"Hospital for Sick Children","funders":"","keywords":"Cohort; Disease; Genetic diagnosis; Cohort study; Genetic testing; Pediatric hospital","score_opus":0.017152034164655376,"score_gpt":0.2588006073856821,"score_spread":0.24164857322102673,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W7116838294","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.99693704,0.00018226185,0.0001240029,0.0000469895,0.0000049711875,0.00003503825,0.0014918557,0.0000104698265,0.0011674329],"genre_scores_gemma":[0.9978142,0.00031653207,0.00020324832,0.00004445289,0.000005772357,0.00002139031,0.001322979,0.0000055357,0.00026586303],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99944013,0.00003030456,0.000025385449,0.0001341481,0.00019111435,0.00017889508],"domain_scores_gemma":[0.99902904,0.000054452248,0.00025906216,0.00005170344,0.0003761066,0.00022968581],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00036793138,0.00038686657,0.00040012505,0.00097022334,0.0017328432,0.00066765764,0.0005951155,0.00024706204,0.0020678963],"category_scores_gemma":[0.0009964496,0.00022091914,0.00027017787,0.001745811,0.0004567119,0.00025374067,0.0005896588,0.00042707924,0.00025295033],"study_design_candidate":"observational","study_design_consensus":"observational","about_ca_topic_candidate":true,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00002714869,0.000011929936,0.9967518,0.000007684884,0.000013870149,0.0008181578,0.00023849656,0.000045433906,0.00037096944,0.000043232772,0.00035808142,0.0013132783],"study_design_scores_gemma":[0.0000041666226,0.000053968484,0.9950058,0.00001336605,0.00001744963,0.0031093839,0.00079693645,0.00010318387,0.00012140952,0.000023811841,0.000744916,0.000005600155],"about_ca_topic_score_codex":0.5937368,"about_ca_topic_score_gemma":0.6258915,"teacher_disagreement_score":0.5937368,"about_ca_system_score_codex":0.0031852939,"about_ca_system_score_gemma":0.007181664,"threshold_uncertainty_score":0.81731147},"labels":[],"label_agreement":null},{"id":"W7116941774","doi":"10.1212/nxg.0000000000200338","title":"NNZ-2591 in Children and Adolescents With Phelan-McDermid Syndrome","year":2025,"lang":"en","type":"article","venue":"Neurology Genetics","topic":"Genomic variations and chromosomal abnormalities","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":"Zynerba Pharmaceuticals; Mallinckrodt Pharmaceuticals; PTC Therapeutics; Ultragenyx Pharmaceutical; National Institutes of Health; Rush University; AveXis; Biogen","keywords":"Incidence (geometry); MEDLINE; Congenital disease; Epidemiology","score_opus":0.0021592205261770597,"score_gpt":0.1878246177877974,"score_spread":0.18566539726162035,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W7116941774","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9900255,0.0074964017,0.000122182,0.00042039115,0.000045271107,0.0001013913,0.00024233993,0.000014654129,0.0015317355],"genre_scores_gemma":[0.996172,0.0026667968,0.00041974892,0.00026216265,0.000020899262,0.000053169308,0.00018716774,0.000002640694,0.0002153776],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9998247,0.00007171167,0.000017832697,0.000027739508,0.000035906327,0.000022119451],"domain_scores_gemma":[0.99961543,0.00012225626,0.00013272068,0.000007121714,0.000021139656,0.00010127458],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00043385994,0.00021307498,0.00056980416,0.00018988844,0.00021335167,0.00021746459,0.00014841827,0.00037185592,0.0009344674],"category_scores_gemma":[0.00086621294,0.00010103451,0.00023881752,0.0002565929,0.00020132736,0.00016466521,0.00016724879,0.0005404707,0.00008979083],"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":[0.039326552,0.0032161826,0.7126216,0.002147064,0.00089796586,0.012486279,0.00080778357,0.0010685333,0.018301604,0.0005970494,0.005669612,0.20285961],"study_design_scores_gemma":[0.011397379,0.03589208,0.90110767,0.00081540796,0.0011908187,0.027816258,0.0010482569,0.0013467878,0.0032105076,0.0004836524,0.015655115,0.00003607891],"about_ca_topic_score_codex":0.0017146645,"about_ca_topic_score_gemma":0.003770884,"teacher_disagreement_score":0.0017146645,"about_ca_system_score_codex":0.00036632054,"about_ca_system_score_gemma":0.00047796362,"threshold_uncertainty_score":0.003409326},"labels":[],"label_agreement":null}]}