{"meta":{"query_hash":"ed813b80d66f","filters":{"topic":"Hereditary Neurological Disorders"},"cohort_total":522,"direct_labels_cover":1,"predictions_cover":522,"exported":522,"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/ed813b80d66f","api":"https://metacan.xera.ac/api/v1/cohort?topic=Hereditary+Neurological+Disorders"},"results":[{"id":"W1096725947","doi":"10.1016/j.ejmg.2015.08.001","title":"Identification of a novel homozygous SPG7 mutation by whole exome sequencing in a Greek family with a complicated form of hereditary spastic paraplegia","year":2015,"lang":"en","type":"article","venue":"European Journal of Medical Genetics","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":14,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"McGill University; Montreal Neurological Institute and Hospital","funders":"Canadian Institutes of Health Research; European Commission; Broad Institute; Muscular Dystrophy Association","keywords":"Exome sequencing; Hereditary spastic paraplegia; Genetics; Frameshift mutation; Biology; Exon; Mutation; Gene; Exome; Genetic heterogeneity; Sanger sequencing; Phenotype","score_opus":0.07997453001907888,"score_gpt":0.27880164001607183,"score_spread":0.19882710999699293,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1096725947","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":[0.9959527,0.000209386,0.0015628731,0.00025440496,0.000033058313,0.000034329078,0.00022462594,0.000041875275,0.0016867347],"genre_scores_gemma":[0.9982687,0.00010970507,0.0008896248,0.00009240587,0.000024181954,0.00001000962,0.00011479125,0.000019554984,0.00047104436],"study_design_codex":"case_report","study_design_gemma":"observational","domain_scores_codex":[0.99975103,0.000030642317,0.000038646223,0.0000843712,0.0000568589,0.000038506754],"domain_scores_gemma":[0.9993974,0.00029824855,0.000084425694,0.00004080108,0.000052348063,0.00012679189],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00020859131,0.0013259288,0.0006481011,0.001002606,0.0007722622,0.0005102579,0.00066280516,0.0017289502,0.0027547718],"category_scores_gemma":[0.0014346814,0.00035391367,0.0007306377,0.0007192639,0.00082923635,0.0003493115,0.0009247534,0.0005874892,0.0005142552],"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":[0.00008649979,0.00003937345,0.016051866,0.00004052181,0.000044558772,0.95820373,0.00046671086,0.0003006606,0.020886673,0.0003617376,0.00025504202,0.0032626009],"study_design_scores_gemma":[0.00004541194,0.00020279856,0.044187594,0.000043708405,0.0001310519,0.943865,0.00039195022,0.00220979,0.00667485,0.00090946705,0.0013077954,0.00003065134],"about_ca_topic_score_codex":0.0009682674,"about_ca_topic_score_gemma":0.0008853164,"teacher_disagreement_score":0.0027547718,"about_ca_system_score_codex":0.00029471595,"about_ca_system_score_gemma":0.00034143237,"threshold_uncertainty_score":0.009215653},"labels":[],"label_agreement":null},{"id":"W143962923","doi":"10.1007/978-3-319-07311-8_1","title":"Peripheral Neuropathy and the Role of Nerve Biopsy","year":2014,"lang":"en","type":"book-chapter","venue":"","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":6,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Sunnybrook Hospital; University of Toronto; Sunnybrook Health Science Centre; St. Michael's Hospital","funders":"","keywords":"Subclinical infection; Medicine; Polyneuropathy; Peripheral neuropathy; Incidence (geometry); Nerve biopsy; Population; Disease; Parkinsonism; Peripheral; Biopsy; Dermatology; Pathology; Internal medicine; Diabetes mellitus; Endocrinology","score_opus":0.015599191860024186,"score_gpt":0.20654383385124955,"score_spread":0.19094464199122538,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W143962923","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":[0.001052736,0.65449834,0.012404498,0.01760707,0.00870893,0.000035070403,0.00014454758,0.00020957747,0.30533928],"genre_scores_gemma":[0.015454661,0.5190597,0.017491028,0.023356238,0.012786922,0.00012596074,0.0002217743,0.00025283088,0.41125086],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.99977607,0.00006862707,0.000013573118,0.00003153327,0.00009383457,0.000016410479],"domain_scores_gemma":[0.9994424,0.00042288445,0.000015482208,0.000020691501,0.00006393429,0.000034513323],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0006917722,0.00068679755,0.0005969407,0.0016087681,0.00037282106,0.0014612582,0.0008151088,0.002468899,0.013035082],"category_scores_gemma":[0.001306001,0.0002803689,0.0002986128,0.0007262428,0.0017674513,0.0022895902,0.0010278842,0.003004553,0.0054627815],"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":[0.00006669238,0.0000833363,0.00024748218,0.0008720034,0.000017247185,0.0012473365,0.00026383207,0.000953523,0.0012158449,0.113415286,0.34333178,0.53828555],"study_design_scores_gemma":[0.000007837598,0.00003040393,0.00042805527,0.0010529029,0.000006800065,0.0049962974,0.00010648237,0.00029737898,0.00026166782,0.0694993,0.9232911,0.000021883054],"about_ca_topic_score_codex":0.0012020991,"about_ca_topic_score_gemma":0.004047781,"teacher_disagreement_score":0.013035082,"about_ca_system_score_codex":0.00089215266,"about_ca_system_score_gemma":0.00085872307,"threshold_uncertainty_score":0.0436067},"labels":[],"label_agreement":null},{"id":"W1538799821","doi":"10.1111/ahg.12017","title":"A Novel Mutation in <i>FGD4/FRABIN</i> Causes Charcot Marie Tooth Disease Type 4H in Patients from a Consanguineous Tunisian Family","year":2013,"lang":"en","type":"article","venue":"Annals of Human Genetics","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":19,"is_retracted":false,"has_abstract":true,"route_ca_aff":false,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"","funders":"Agence Universitaire de la Francophonie","keywords":"Consanguinity; Genetic heterogeneity; Frameshift mutation; Genetics; Medicine; Hereditary motor and sensory neuropathy; Founder effect; Consanguineous Marriage; Mutation; Phenotype; Disease; Tooth disease; Age of onset; Chinese family; Biology; Genotype; Gene; Pathology; Haplotype","score_opus":0.0888000202915497,"score_gpt":0.3019097663530389,"score_spread":0.2131097460614892,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1538799821","genre_codex":"empirical","genre_gemma":"empirical","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"empirical","genre_consensus":"empirical","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9990476,0.00016934637,0.0001764013,0.00009046874,0.0000103647235,0.00001443264,0.00006424647,0.000014350812,0.00041284304],"genre_scores_gemma":[0.99916244,0.00009087781,0.00022793011,0.000097283664,0.000018590905,0.000006189599,0.000055684246,0.000006124832,0.0003348979],"study_design_codex":"case_report","study_design_gemma":"observational","domain_scores_codex":[0.99974924,0.000033929344,0.000029144063,0.00008036106,0.000043769116,0.00006356065],"domain_scores_gemma":[0.99973685,0.000060765895,0.00009229393,0.000013580432,0.000023112794,0.000073470525],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0001659133,0.0011398352,0.00040910873,0.0010239235,0.0012788057,0.00042673352,0.00047070035,0.0008681158,0.0015148369],"category_scores_gemma":[0.0009446888,0.00041790755,0.00044643943,0.0007404689,0.00067992357,0.00020903432,0.00046692014,0.00044523622,0.00019954602],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00067067926,0.00021625223,0.38422,0.00013241112,0.0002240905,0.53872794,0.0032764615,0.00043583618,0.051794183,0.00029424235,0.0010604995,0.018947434],"study_design_scores_gemma":[0.00012842136,0.0004251979,0.4663179,0.000053623102,0.0001987079,0.52109736,0.000990282,0.0008849838,0.006361458,0.00017856136,0.0033014754,0.000062106614],"about_ca_topic_score_codex":0.014819091,"about_ca_topic_score_gemma":0.012477396,"teacher_disagreement_score":0.014819091,"about_ca_system_score_codex":0.0008773454,"about_ca_system_score_gemma":0.0004234387,"threshold_uncertainty_score":0.029465675},"labels":[],"label_agreement":null},{"id":"W1546232506","doi":"","title":"The Bournemouth Questionnaire as an outcome measure in the rehabilitation of a person suffering with mechanical neck and arm pain and concurrent Charcot-Marie-Tooth disease: a case report.","year":2006,"lang":"en","type":"article","venue":"PubMed","topic":"Hereditary Neurological Disorders","field":"Neuroscience","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":"Canada Research Chairs","funders":"","keywords":"Medicine; Rehabilitation; Neck pain; Physical therapy; Disease; Tooth disease; Physical medicine and rehabilitation; Alternative medicine; Pathology","score_opus":0.029925083025726537,"score_gpt":0.24986973299384418,"score_spread":0.21994464996811763,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1546232506","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":[0.99783856,0.0008998815,0.0003994152,0.00014257188,0.000023787055,0.00004558497,0.000043636086,0.000005097536,0.0006013831],"genre_scores_gemma":[0.9989675,0.0002421628,0.00048401783,0.000054535,0.000038102913,0.000027213659,0.000035149547,0.0000014587143,0.00014976838],"study_design_codex":"observational","study_design_gemma":"case_report","domain_scores_codex":[0.9991654,0.0003549717,0.00008875631,0.00009215527,0.00016947313,0.0001292868],"domain_scores_gemma":[0.9980464,0.00083859055,0.0007052948,0.00005969925,0.00013387442,0.00021618966],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0012601177,0.0004470601,0.00037601189,0.0010163351,0.0004885377,0.0005328001,0.00041859754,0.001166993,0.0006279085],"category_scores_gemma":[0.003418317,0.0002323124,0.0003546104,0.0007077715,0.00066413236,0.00072924723,0.00049923704,0.0005323084,0.00014855065],"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":[0.00030865957,0.0003265167,0.8205049,0.00024402878,0.0000566906,0.16001628,0.0020325328,0.00013333178,0.0036309103,0.00014605332,0.00043350254,0.012166598],"study_design_scores_gemma":[0.000051741463,0.0019092282,0.5714765,0.00009373288,0.00008556864,0.41945142,0.0029402485,0.00066789874,0.0013722447,0.000081102575,0.001812168,0.00005809482],"about_ca_topic_score_codex":0.0010952876,"about_ca_topic_score_gemma":0.0013042787,"teacher_disagreement_score":0.0012601177,"about_ca_system_score_codex":0.00035332202,"about_ca_system_score_gemma":0.00037438227,"threshold_uncertainty_score":0.0066642165},"labels":[],"label_agreement":null},{"id":"W1558601431","doi":"10.1002/mus.23968","title":"An atypical case of <i>SCN9A</i> mutation presenting with global motor delay and a severe pain disorder","year":2013,"lang":"en","type":"review","venue":"Muscle & Nerve","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":25,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Centre Hospitalier Universitaire Sainte-Justine","funders":"","keywords":"Erythromelalgia; Missense mutation; Muscle biopsy; Medicine; Neuropathic pain; Skin biopsy; Anesthesia; Atrophy; Global developmental delay; Neuroscience; Psychology; Biopsy; Internal medicine; Mutation; Biology; Phenotype; Genetics; Gene","score_opus":0.0409427199170613,"score_gpt":0.306408918613246,"score_spread":0.2654661986961847,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1558601431","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":[0.06344716,0.91523194,0.0036649911,0.0018546715,0.0010492528,0.00007004488,0.0001509817,0.00015082902,0.014380052],"genre_scores_gemma":[0.41982654,0.5661623,0.0032127637,0.0021573887,0.0020141387,0.000041916646,0.00039038857,0.000035791,0.006158866],"study_design_codex":"case_report","study_design_gemma":"case_report","domain_scores_codex":[0.99986863,0.000017562625,0.00002347881,0.000037718142,0.00002334075,0.000029273124],"domain_scores_gemma":[0.9998523,0.00004458823,0.000052412364,0.0000064709366,0.0000138240175,0.000030295354],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00013105766,0.0011881064,0.00086723577,0.0015374749,0.00021308576,0.00045667752,0.0006512558,0.0015739137,0.0012753772],"category_scores_gemma":[0.0003802987,0.00018863496,0.00036063284,0.0011062546,0.0005832101,0.0006168784,0.00040081277,0.0007297321,0.0008566101],"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":[0.00011345814,0.00006334391,0.0040162867,0.0031549877,0.00009476827,0.79877293,0.00019862759,0.00042907358,0.0110781025,0.0012427105,0.010491132,0.17034459],"study_design_scores_gemma":[0.000019279392,0.00004814457,0.0029329853,0.0002804492,0.00004545305,0.9742294,0.000060277038,0.00010307059,0.00066873716,0.0003079339,0.021290608,0.000013618084],"about_ca_topic_score_codex":0.0010485342,"about_ca_topic_score_gemma":0.0016251705,"teacher_disagreement_score":0.0015739137,"about_ca_system_score_codex":0.00032900428,"about_ca_system_score_gemma":0.00044917842,"threshold_uncertainty_score":0.0042666197},"labels":[],"label_agreement":null},{"id":"W1560210569","doi":"10.1034/j.1399-0004.2000.570603.x","title":"Genetic landmarks through philately – Jean Martin Charcot (1825–1893) and Charcot–Marie–Tooth disease","year":2000,"lang":"en","type":"article","venue":"Clinical Genetics","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":1,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Manitoba","funders":"","keywords":"Philately; Tooth disease; Section (typography); Citation; Gerontology; Library science; Medicine; Genealogy; History; Disease; Computer science; Pathology; Archaeology","score_opus":0.09378676125263671,"score_gpt":0.3409745002616177,"score_spread":0.24718773900898097,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1560210569","genre_codex":"empirical","genre_gemma":"other","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"other","genre_consensus":null,"domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.77270293,0.02461201,0.003831809,0.029708533,0.0029717125,0.00011065913,0.0014544196,0.00020956538,0.16439848],"genre_scores_gemma":[0.9286872,0.0105054695,0.002784507,0.0022597807,0.0012548243,0.000042519365,0.00028556865,0.00007944451,0.054100607],"study_design_codex":"case_report","study_design_gemma":"not_applicable","domain_scores_codex":[0.9997173,0.00005849383,0.000027891676,0.000074788564,0.000051352872,0.0000701085],"domain_scores_gemma":[0.9994454,0.0001646005,0.00017115385,0.000019864734,0.000106117805,0.00009280207],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00027383157,0.0007261045,0.00039245794,0.0013179497,0.0021004404,0.00063006324,0.00035374888,0.0020618702,0.005260523],"category_scores_gemma":[0.0015519467,0.00027652676,0.00029877343,0.0010919637,0.0017952422,0.0007798066,0.0007704404,0.0013130058,0.00071327476],"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":[0.0019743,0.0003519231,0.037272174,0.00036546015,0.0002413108,0.5817,0.005724407,0.0019183251,0.040548928,0.11039781,0.055415817,0.16408952],"study_design_scores_gemma":[0.00016005909,0.00026471552,0.093780115,0.00028993186,0.00020277852,0.3836165,0.0013231979,0.0005016902,0.010400539,0.017114604,0.49216062,0.0001851747],"about_ca_topic_score_codex":0.018879643,"about_ca_topic_score_gemma":0.026455894,"teacher_disagreement_score":0.018879643,"about_ca_system_score_codex":0.0012925903,"about_ca_system_score_gemma":0.0014231984,"threshold_uncertainty_score":0.03753954},"labels":[],"label_agreement":null},{"id":"W1565329788","doi":"10.1002/9781444345100.ch36","title":"Charcot–Marie–Tooth Disease and the Treatment of the Cavo‐Varus Foot","year":2011,"lang":"en","type":"other","venue":"Evidence-Based Orthopedics","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":false,"ca_institutions":"University of British Columbia","funders":"","keywords":"Tooth disease; Foot (prosody); Orthodontics; Medicine; Geology; Disease; Art; Pathology","score_opus":0.07488138692773115,"score_gpt":0.2669159031549561,"score_spread":0.19203451622722495,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1565329788","genre_codex":"empirical","genre_gemma":"other","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"other","genre_consensus":null,"domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.3599348,0.3130076,0.0011764773,0.014487495,0.000869263,0.00010320868,0.00034612755,0.00023849522,0.30983654],"genre_scores_gemma":[0.8575237,0.09080781,0.0019010465,0.0037764318,0.0010949066,0.00009515303,0.00041408266,0.00003318525,0.044353724],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.9999112,0.000024454148,0.00000815445,0.000007121437,0.0000289599,0.0000201513],"domain_scores_gemma":[0.99987006,0.00003133725,0.00003053604,0.000006392271,0.000017761357,0.00004395391],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00022773324,0.00030381716,0.00031370556,0.0008725983,0.0006767126,0.00039924373,0.00027547788,0.00067511125,0.005419289],"category_scores_gemma":[0.00035906062,0.000070237795,0.00020388854,0.0007529638,0.00021978567,0.0001551743,0.00024124773,0.0005725171,0.0008324339],"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":[0.0029559294,0.0040586432,0.030470112,0.0021202608,0.00039233026,0.10837018,0.00028869638,0.0011820013,0.013334508,0.00728675,0.05736386,0.7721766],"study_design_scores_gemma":[0.0022745414,0.0031218657,0.18100448,0.0022316733,0.00055459276,0.2963124,0.00059669843,0.0018389749,0.004661131,0.010534976,0.49678004,0.000088700064],"about_ca_topic_score_codex":0.0035261367,"about_ca_topic_score_gemma":0.014326394,"teacher_disagreement_score":0.005419289,"about_ca_system_score_codex":0.0005136034,"about_ca_system_score_gemma":0.0005819557,"threshold_uncertainty_score":0.01812929},"labels":[],"label_agreement":null},{"id":"W1589042524","doi":"10.1038/85817","title":"SPTLC1 is mutated in hereditary sensory neuropathy, type 1","year":2001,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":293,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Toronto Western Hospital","funders":"","keywords":"Biology; Genetics; Locus (genetics); Sensory neuropathy; Gene; Sensory system; Dorsum; Anatomy; Neuroscience; Internal medicine; Medicine","score_opus":0.02978553828112258,"score_gpt":0.2801146467568478,"score_spread":0.2503291084757252,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1589042524","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":[0.99208415,0.0010272423,0.0012614088,0.00046344663,0.00013075193,0.00003315866,0.0008667518,0.00017127277,0.0039617773],"genre_scores_gemma":[0.9975387,0.00018111974,0.0006862795,0.00009153456,0.000050300983,0.000010555512,0.00033784498,0.00003768735,0.0010659256],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.99977404,0.00001913817,0.000026266644,0.000060705137,0.00007968072,0.000040189207],"domain_scores_gemma":[0.99942636,0.00019309009,0.00016021615,0.000021454782,0.00006600702,0.00013282968],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0001765664,0.0010828824,0.00055378483,0.0014048062,0.0008880156,0.00046025414,0.00089602784,0.002054641,0.004556308],"category_scores_gemma":[0.0010703513,0.00021668285,0.00039113933,0.0008789314,0.00076402625,0.00030831926,0.000536994,0.00077743485,0.00075885985],"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":[0.0030254624,0.00029812066,0.053173535,0.00059195835,0.00029332805,0.39294544,0.0010189336,0.0023529227,0.50293297,0.0024325927,0.0073720207,0.033562705],"study_design_scores_gemma":[0.0005512145,0.00072567986,0.23643391,0.00031652246,0.0007492247,0.5304211,0.00090759736,0.010609583,0.20298272,0.0035152212,0.012595354,0.00019190725],"about_ca_topic_score_codex":0.0041070515,"about_ca_topic_score_gemma":0.0030596256,"teacher_disagreement_score":0.004556308,"about_ca_system_score_codex":0.00061733864,"about_ca_system_score_gemma":0.00038273024,"threshold_uncertainty_score":0.015242338},"labels":[],"label_agreement":null},{"id":"W1603758951","doi":"10.1016/j.ajhg.2008.12.010","title":"Deleterious Variants of FIG4, a Phosphoinositide Phosphatase, in Patients with ALS","year":2009,"lang":"nl","type":"book-chapter","venue":"The American Journal of Human Genetics","topic":"Hereditary Neurological Disorders","field":"Neuroscience","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":"Alzheimer Society of Canada","funders":"National Institute of Neurological Disorders and Stroke; National Institute of General Medical Sciences; ALS Association; ALS Therapy Alliance; National Institutes of Health; Howard Hughes Medical Institute","keywords":"Amyotrophic lateral sclerosis; Biology; Nonsynonymous substitution; Gene; Biochemistry; Genetics; Disease; Medicine; Pathology","score_opus":0.016830234804447446,"score_gpt":0.24073961851307715,"score_spread":0.2239093837086297,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1603758951","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":[0.11123153,0.13301219,0.02608605,0.0273038,0.003382072,0.00008995309,0.0044307285,0.0026744788,0.69178927],"genre_scores_gemma":[0.19608341,0.054007094,0.018441945,0.009202831,0.0017939371,0.00007994849,0.0028056777,0.00049651944,0.7170886],"study_design_codex":"design_other","study_design_gemma":"observational","domain_scores_codex":[0.99996865,0.000005457932,0.0000025662694,0.000007178703,0.000013174035,0.0000029067357],"domain_scores_gemma":[0.9999429,0.00003965298,0.0000034151642,0.000001871261,0.000005947201,0.0000061236797],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00008109746,0.00029905757,0.00019296978,0.0004595343,0.00012468534,0.00021607938,0.00020839492,0.0004901955,0.020446267],"category_scores_gemma":[0.0002570834,0.00011198555,0.00008671355,0.00022988908,0.00022446453,0.00037765055,0.00022667326,0.0003974118,0.0052197543],"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":[0.00018605022,0.000044557746,0.006340284,0.0003581704,0.000018011833,0.0062251426,0.0004560094,0.0009780265,0.012741085,0.011808765,0.41094536,0.5498985],"study_design_scores_gemma":[0.00004640406,0.00017613609,0.018982207,0.00038581036,0.00002989772,0.045888443,0.00016759406,0.0016308276,0.0048194393,0.017901544,0.9099419,0.00002976872],"about_ca_topic_score_codex":0.0005702143,"about_ca_topic_score_gemma":0.0018119256,"teacher_disagreement_score":0.020446267,"about_ca_system_score_codex":0.00025967567,"about_ca_system_score_gemma":0.00012294944,"threshold_uncertainty_score":0.06839961},"labels":[],"label_agreement":null},{"id":"W1607326855","doi":"10.1002/9781118618424.ch15","title":"Hereditary neuropathy with liability to pressure palsy","year":2014,"lang":"en","type":"other","venue":"","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":1,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Université de Montréal","funders":"","keywords":"Liability; Medicine; Palsy; Physical medicine and rehabilitation; Business; Pathology; Alternative medicine; Finance","score_opus":0.01606254532164921,"score_gpt":0.2320076082188324,"score_spread":0.21594506289718318,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1607326855","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":[0.51755345,0.0052601458,0.0047649955,0.002131746,0.00024524704,0.00012464504,0.00568561,0.00046390813,0.46377024],"genre_scores_gemma":[0.8685373,0.0023182423,0.0020916418,0.0003927705,0.00023074014,0.000037504095,0.0036982964,0.00012068683,0.12257266],"study_design_codex":"observational","study_design_gemma":"case_report","domain_scores_codex":[0.99976295,0.00002892803,0.000017250504,0.00003795547,0.00007047061,0.00008246261],"domain_scores_gemma":[0.99954957,0.00009166312,0.00009595911,0.00003461744,0.00009745807,0.00013072712],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00024895917,0.0007066116,0.00023961467,0.0022948168,0.0011758937,0.00053198455,0.00044161797,0.00058493833,0.034591313],"category_scores_gemma":[0.0010260826,0.000096928234,0.00028911125,0.0014661491,0.00042115373,0.0004350442,0.00077219924,0.0004401835,0.0024906988],"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":[0.0012718624,0.00079946377,0.35223982,0.00063822995,0.00024654414,0.24411379,0.0010137531,0.001868948,0.0136211375,0.049603805,0.07514616,0.2594365],"study_design_scores_gemma":[0.00016013243,0.0002868675,0.42530662,0.00070472184,0.00038142817,0.37263286,0.0010797441,0.0031846336,0.012900423,0.02076049,0.1625379,0.0000642606],"about_ca_topic_score_codex":0.0076827416,"about_ca_topic_score_gemma":0.010213565,"teacher_disagreement_score":0.034591313,"about_ca_system_score_codex":0.00047011,"about_ca_system_score_gemma":0.0008148805,"threshold_uncertainty_score":0.1157195},"labels":[],"label_agreement":null},{"id":"W168928810","doi":"10.1007/bf03016671","title":"Ultrasound-guided peripheral regional blockade in patients with Charcot-Marie-Tooth disease: a review of three cases","year":2008,"lang":"en","type":"review","venue":"Canadian Journal of Anesthesia/Journal canadien d anesthésie","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":38,"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 Joseph's Health Care; Western University","funders":"","keywords":"Medicine; Tooth disease; Surgery; Local anesthetic; Exacerbation; Blockade; Presentation (obstetrics); Peripheral; Ultrasound; Anesthesia; Motor nerve; Disease; Anatomy; Radiology; Pathology; Internal medicine","score_opus":0.042159023863611776,"score_gpt":0.256876484446097,"score_spread":0.21471746058248523,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W168928810","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":[0.003168664,0.99442035,0.00065304636,0.00033110596,0.0001344514,0.000009651878,0.000024214445,0.000022509405,0.0012360178],"genre_scores_gemma":[0.022302669,0.9747772,0.0012658099,0.00065071986,0.00041450784,0.000012509242,0.00008249088,0.000010684315,0.00048333674],"study_design_codex":"design_other","study_design_gemma":"case_report","domain_scores_codex":[0.9995987,0.000059353162,0.00011471015,0.000089533045,0.000100660094,0.000037031412],"domain_scores_gemma":[0.9992274,0.00044983346,0.0001405002,0.000029848017,0.00008675485,0.00006567369],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00044234074,0.0012315301,0.0016221335,0.0033585874,0.00041325012,0.000901857,0.001759596,0.0016944509,0.0011920343],"category_scores_gemma":[0.001429056,0.00042216206,0.00086288527,0.0025979201,0.0008460815,0.0015609359,0.0005929789,0.0011633802,0.0008046785],"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":[0.00018073616,0.00018418595,0.008279741,0.012921911,0.0003998296,0.115599595,0.00059481274,0.00061055756,0.00427747,0.0008553586,0.018390499,0.8377054],"study_design_scores_gemma":[0.000067900815,0.00022509336,0.016674858,0.006851755,0.0009796782,0.78607553,0.0008097216,0.00041363775,0.002105152,0.0010377447,0.1846016,0.00015742969],"about_ca_topic_score_codex":0.00140849,"about_ca_topic_score_gemma":0.0025883708,"teacher_disagreement_score":0.0033585874,"about_ca_system_score_codex":0.0005274372,"about_ca_system_score_gemma":0.00069940556,"threshold_uncertainty_score":0.0039877295},"labels":[],"label_agreement":null},{"id":"W1851604172","doi":"10.1002/mus.24640","title":"Phenotypic variability of CMT4C in a French‐Canadian kindred","year":2015,"lang":"en","type":"article","venue":"Muscle & Nerve","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":24,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":true,"ca_institutions":"University of Ottawa; McMaster University; McMaster University Medical Centre","funders":"","keywords":"Pes cavus; Scoliosis; Proband; Medicine; Weakness; Age of onset; Deformity; Pediatrics; Genetics; Surgery; Internal medicine; Biology; Gene; Mutation; Disease; Complication","score_opus":0.062361832599678445,"score_gpt":0.25403417192594563,"score_spread":0.19167233932626718,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1851604172","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":[0.9924495,0.0006116394,0.00044849468,0.00031923383,0.00003053927,0.000040257208,0.00074761914,0.000041065934,0.005311565],"genre_scores_gemma":[0.99680483,0.00032187803,0.0007732433,0.00013592622,0.000018519551,0.000015910498,0.00039985488,0.000021866112,0.001507944],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9992792,0.000068065536,0.00004735192,0.0001828286,0.00024870617,0.00017377365],"domain_scores_gemma":[0.999321,0.00015884239,0.00011535617,0.000027804494,0.00023243036,0.0001446213],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0004913037,0.0022314675,0.0005452566,0.0024093117,0.0034300603,0.00065260625,0.00083095115,0.0009927531,0.0044178097],"category_scores_gemma":[0.0017085376,0.0003309904,0.00062314776,0.0019582347,0.0012060835,0.00021004926,0.0008991405,0.00042699132,0.00042518767],"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":[0.0012556801,0.00015407555,0.5211517,0.00032413495,0.00037571904,0.35808924,0.010706802,0.0013866464,0.05082825,0.0023419117,0.0085462425,0.044839595],"study_design_scores_gemma":[0.00009227657,0.00021048337,0.6748685,0.00018513617,0.00029490452,0.30518028,0.0028348279,0.0009537164,0.0028761576,0.0003573259,0.012014292,0.00013199201],"about_ca_topic_score_codex":0.5813245,"about_ca_topic_score_gemma":0.6180816,"teacher_disagreement_score":0.41867548,"about_ca_system_score_codex":0.0036213,"about_ca_system_score_gemma":0.003886385,"threshold_uncertainty_score":0.8422823},"labels":[],"label_agreement":null},{"id":"W1881534980","doi":"10.1093/pch/13.2.121a","title":"Case 2: Long-standing neuropathy with acute onset of weakness","year":2008,"lang":"en","type":"article","venue":"Paediatrics & Child Health","topic":"Hereditary Neurological Disorders","field":"Neuroscience","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":"Children's Hospital of Eastern Ontario","funders":"","keywords":"Medicine; Aunt; Presentation (obstetrics); Physical examination; Weakness; Surgery; Pes cavus; Family history; Neurological examination; Pediatrics; Physical therapy; Complication","score_opus":0.0355879998950069,"score_gpt":0.27032119986479014,"score_spread":0.23473319996978326,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1881534980","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":[0.9800971,0.0018683895,0.0021167467,0.0033259036,0.0003904582,0.00022411867,0.00024245374,0.00012467291,0.0116101215],"genre_scores_gemma":[0.99310994,0.00085275085,0.0011508081,0.0013129987,0.00084570085,0.00007545345,0.00015972518,0.000032374966,0.0024603377],"study_design_codex":"case_report","study_design_gemma":"case_report","domain_scores_codex":[0.9989465,0.000117188625,0.00011933858,0.00022401992,0.00012854449,0.00046449268],"domain_scores_gemma":[0.997769,0.000675574,0.00048603283,0.00014843959,0.0001263572,0.0007946653],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00060105283,0.0027950346,0.001273344,0.0014062439,0.002760862,0.001630458,0.0015550057,0.0063145533,0.00434164],"category_scores_gemma":[0.0046183974,0.0011155056,0.0011589697,0.001410824,0.0014214863,0.0025913862,0.0018795567,0.0031724898,0.0013403159],"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":[0.000030479063,0.00004411566,0.0057045445,0.000019510411,0.0000037959726,0.99312615,0.000104887804,0.000033286942,0.00020396714,0.00007053757,0.000117455995,0.00054123206],"study_design_scores_gemma":[0.000021122449,0.00010042401,0.0044209557,0.0000132486075,0.0000042931115,0.9948775,0.00009721823,0.000074676915,0.00008252748,0.00009272276,0.00020849059,0.00000683147],"about_ca_topic_score_codex":0.0029178413,"about_ca_topic_score_gemma":0.0038017428,"teacher_disagreement_score":0.0063145533,"about_ca_system_score_codex":0.0011508666,"about_ca_system_score_gemma":0.0011187802,"threshold_uncertainty_score":0.014524221},"labels":[],"label_agreement":null},{"id":"W1896319811","doi":"10.1016/j.nmd.2015.06.463","title":"Hereditary neuropathy with liability to pressure palsies in childhood: Case series and literature update","year":2015,"lang":"en","type":"article","venue":"Neuromuscular Disorders","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":31,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Hospital for Sick Children; University of Toronto; SickKids Foundation; Western University; Montreal Children's Hospital; McGill University; Children's Hospital of Eastern Ontario; Children’s Health Research Institute; University of Ottawa","funders":"","keywords":"Liability; Series (stratigraphy); Medicine; Political science; Law; Biology","score_opus":0.01124976476134495,"score_gpt":0.2183627765605848,"score_spread":0.20711301179923985,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1896319811","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":[0.29491454,0.6478045,0.005901829,0.007646794,0.0028629147,0.00035401247,0.0016158848,0.00046515182,0.038434435],"genre_scores_gemma":[0.5721744,0.40164787,0.006409228,0.00409356,0.009315567,0.0001123959,0.001554095,0.000085976135,0.004606975],"study_design_codex":"case_report","study_design_gemma":"case_report","domain_scores_codex":[0.99938333,0.00006401061,0.00022392582,0.00012025444,0.00008395048,0.00012441937],"domain_scores_gemma":[0.9981065,0.00070159644,0.000571744,0.00010841379,0.00025817505,0.0002535246],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00044303745,0.0015080789,0.001362457,0.004912855,0.0010816164,0.0022275173,0.0014522265,0.0032927918,0.0036187547],"category_scores_gemma":[0.0027654383,0.0006166638,0.00092457805,0.0031402437,0.0012999009,0.0029892116,0.0012968848,0.0012484138,0.0016933549],"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":[0.000064462634,0.00012476605,0.02774783,0.0011528513,0.000095977266,0.9147602,0.00054249965,0.00024411846,0.001128952,0.00040765485,0.008817126,0.044913568],"study_design_scores_gemma":[0.000008954854,0.000021524378,0.007958262,0.00039843694,0.00012254581,0.98094463,0.0004559134,0.00009358533,0.0002565609,0.00030007138,0.009410302,0.000029151852],"about_ca_topic_score_codex":0.0017722853,"about_ca_topic_score_gemma":0.0027034688,"teacher_disagreement_score":0.004912855,"about_ca_system_score_codex":0.00083286205,"about_ca_system_score_gemma":0.0010819285,"threshold_uncertainty_score":0.012105942},"labels":[],"label_agreement":null},{"id":"W1965654940","doi":"10.1016/j.neurobiolaging.2011.11.012","title":"Exome sequencing reveals SPG11 mutations causing juvenile ALS","year":2011,"lang":"nl","type":"article","venue":"Neurobiology of Aging","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":100,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Université de Montréal; Centre Hospitalier de l’Université de Montréal","funders":"Canadian Institutes of Health Research","keywords":"Hereditary spastic paraplegia; Exome sequencing; Amyotrophic lateral sclerosis; Frameshift mutation; Genetics; Exon; Phenotype; Exome; Biology; Mutation; Medicine; Gene; Disease; Pathology","score_opus":0.1021930238196486,"score_gpt":0.2827418696963239,"score_spread":0.1805488458766753,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1965654940","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":[0.9940958,0.0002799731,0.000995861,0.0005765836,0.00005818605,0.000020777568,0.0008839123,0.00007554002,0.0030133734],"genre_scores_gemma":[0.9949516,0.00021374687,0.0012169664,0.00024353109,0.000041158077,0.000010471849,0.0005914977,0.000030467136,0.0027005868],"study_design_codex":"case_report","study_design_gemma":"observational","domain_scores_codex":[0.9997862,0.000018138928,0.00003528776,0.00006216319,0.00005938213,0.000038914837],"domain_scores_gemma":[0.99960893,0.0001765723,0.000051642357,0.000019896313,0.000047841422,0.00009529041],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00021211519,0.0011347644,0.0003645852,0.00093695294,0.00067916064,0.0006613702,0.0004914201,0.0025418485,0.004426308],"category_scores_gemma":[0.000595625,0.00024852256,0.0004986445,0.00052107725,0.00057658675,0.00042743504,0.00050674484,0.0007163662,0.0009043304],"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":[0.0007379319,0.0002061426,0.043852568,0.0001686355,0.00013130391,0.64499617,0.0011648546,0.0012293465,0.27561572,0.0011386654,0.0032139837,0.027544715],"study_design_scores_gemma":[0.00015153878,0.0008649102,0.2668431,0.0001048079,0.00032828288,0.62322855,0.0015219379,0.005184974,0.088204324,0.0029420212,0.01052832,0.00009723227],"about_ca_topic_score_codex":0.0020805914,"about_ca_topic_score_gemma":0.0035337382,"teacher_disagreement_score":0.004426308,"about_ca_system_score_codex":0.0004161022,"about_ca_system_score_gemma":0.0002786692,"threshold_uncertainty_score":0.014807463},"labels":[],"label_agreement":null},{"id":"W1966700432","doi":"10.1139/g01-103","title":"α-Catulin maps to the familial dysautonomia region on 9q31","year":2001,"lang":"en","type":"article","venue":"Genome","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":1,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":true,"route_about_ca":false,"ca_institutions":"Hospital for Sick Children","funders":"Canadian Institutes of Health Research; University of Toronto","keywords":"Transversion; Familial dysautonomia; Genetics; Biology; Linkage disequilibrium; Exon; Population; Disease; Dysautonomia; Genotype; Gene; Single-nucleotide polymorphism; Medicine; Internal medicine","score_opus":0.051045417706789505,"score_gpt":0.2508857177151349,"score_spread":0.1998403000083454,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1966700432","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":[0.99577445,0.001041629,0.00087738724,0.00012289055,0.000020214335,0.000021550926,0.00011708742,0.000034077693,0.0019907122],"genre_scores_gemma":[0.99812716,0.00024220288,0.00075838505,0.00003415997,0.000016075648,0.000009196049,0.00015677902,0.0000034104226,0.00065261114],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9998424,0.000023254399,0.0000137458965,0.000053538115,0.00004433685,0.000022750248],"domain_scores_gemma":[0.99979573,0.000050378414,0.000084466745,0.000012497021,0.000029345563,0.000027607226],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00012270184,0.00041300693,0.0003210877,0.0007066712,0.0004816814,0.0002083665,0.00029424904,0.00052872754,0.0028584334],"category_scores_gemma":[0.00049427355,0.00018128357,0.00021318106,0.00038752507,0.00027405616,0.000119531534,0.0002658962,0.00026814337,0.0005877357],"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":[0.0016693491,0.00020587198,0.1345077,0.00024155909,0.0002635723,0.0787073,0.0014591058,0.0011672872,0.7191175,0.0022990205,0.0015961324,0.058765534],"study_design_scores_gemma":[0.00025777973,0.0005623815,0.8017971,0.0001937258,0.00019484233,0.13158742,0.00034438318,0.0023443406,0.043868445,0.002980525,0.015819103,0.00004998918],"about_ca_topic_score_codex":0.0025376955,"about_ca_topic_score_gemma":0.0033536525,"teacher_disagreement_score":0.0028584334,"about_ca_system_score_codex":0.00036371057,"about_ca_system_score_gemma":0.000151941,"threshold_uncertainty_score":0.009562373},"labels":[],"label_agreement":null},{"id":"W1967308780","doi":"10.1073/pnas.152621799","title":"Association of calnexin with mutant peripheral myelin protein-22 <i>ex vivo</i> : A basis for “gain-of-function” ER diseases","year":2002,"lang":"en","type":"article","venue":"Proceedings of the National Academy of Sciences","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":118,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"McGill University","funders":"","keywords":"Calnexin; Endoplasmic reticulum; Myelin; Colocalization; Calreticulin; Cell biology; Unfolded protein response; Intracellular; Ex vivo; Chemistry; Biology; Molecular biology; Biochemistry; Endocrinology; In vitro","score_opus":0.040783968815467454,"score_gpt":0.26585065046001594,"score_spread":0.2250666816445485,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1967308780","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":[0.991213,0.00076486525,0.0064598103,0.00016890212,0.000053982352,0.0000215842,0.00021870549,0.00017758277,0.00092153606],"genre_scores_gemma":[0.992949,0.000582897,0.0041293637,0.00006143144,0.000012318588,0.000027700018,0.00041044326,0.00007066584,0.0017562538],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9998944,0.000018122493,0.000012618353,0.000034896257,0.000023445627,0.000016467735],"domain_scores_gemma":[0.99987364,0.00001873482,0.00004344808,0.000019978483,0.00001140427,0.0000326704],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00016830335,0.00043111647,0.00020891038,0.00010927993,0.00015631007,0.0003332756,0.00026482827,0.00028632864,0.0007149565],"category_scores_gemma":[0.00013632305,0.00012344118,0.00018301113,0.00006616303,0.00028074606,0.00030024827,0.00027594497,0.00047698512,0.0003572612],"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":[0.000036045127,0.000011402457,0.00012862837,0.0000100737125,0.000002969888,0.00009957134,0.0000053327126,0.000029311383,0.99926573,0.000103721635,0.000019806423,0.00028729223],"study_design_scores_gemma":[0.000010129217,0.00007766137,0.0025579748,0.0000035647552,0.000010850185,0.0009663086,0.00001676853,0.00085915474,0.9938652,0.000071897535,0.0015570108,0.0000034880936],"about_ca_topic_score_codex":0.00025517764,"about_ca_topic_score_gemma":0.00039191716,"teacher_disagreement_score":0.0007149565,"about_ca_system_score_codex":0.0003599282,"about_ca_system_score_gemma":0.000122040794,"threshold_uncertainty_score":0.0026114583},"labels":[],"label_agreement":null},{"id":"W1968946521","doi":"10.1212/01.wnl.0000168898.76071.70","title":"Clinical and electrophysiologic features of CMT2A with mutations in the mitofusin 2 gene","year":2005,"lang":"en","type":"article","venue":"Neurology","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":184,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Geomechanica (Canada)","funders":"National Center for Research Resources; National Institute of Neurological Disorders and Stroke","keywords":"MFN2; Genetics; Biology; Proband; Locus (genetics); Gene; Mutation; Phenotype; Mitochondrial DNA; mitochondrial fusion","score_opus":0.028265149792113326,"score_gpt":0.29609588183455865,"score_spread":0.26783073204244534,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1968946521","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":[0.9973379,0.00035928626,0.00036424588,0.0001196189,0.000011973753,0.000027357013,0.000081670456,0.000019370964,0.0016785002],"genre_scores_gemma":[0.9993647,0.00008243416,0.0002088591,0.00006859334,0.00004152421,0.000010701445,0.000069384034,0.0000054777024,0.00014814932],"study_design_codex":"case_report","study_design_gemma":"observational","domain_scores_codex":[0.99968934,0.00004904299,0.00003816803,0.00008044173,0.00006788132,0.0000751524],"domain_scores_gemma":[0.99896574,0.0003363012,0.00026829663,0.000039290695,0.00010399502,0.00028641828],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0003005728,0.0011965858,0.0003650535,0.0011628779,0.00059797935,0.00035321424,0.00032118012,0.0011299024,0.0026008813],"category_scores_gemma":[0.002121708,0.00026952208,0.000264529,0.0007338406,0.00076050893,0.00033698126,0.00051067077,0.0005851204,0.00041328772],"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":[0.00056393666,0.00029743172,0.43220204,0.000106155865,0.00010308043,0.5174567,0.00073154696,0.0003775113,0.04050379,0.0002383685,0.0009917989,0.006427504],"study_design_scores_gemma":[0.000064109656,0.00030396465,0.22473799,0.000025417754,0.00004398983,0.772165,0.00013428474,0.00030780208,0.0014671062,0.00010300338,0.00063422153,0.000013135511],"about_ca_topic_score_codex":0.0012435172,"about_ca_topic_score_gemma":0.0010886431,"teacher_disagreement_score":0.0026008813,"about_ca_system_score_codex":0.0003297183,"about_ca_system_score_gemma":0.00026269676,"threshold_uncertainty_score":0.008700788},"labels":[],"label_agreement":null},{"id":"W1968980213","doi":"10.1007/s10048-014-0411-3","title":"AIMP1 deficiency presents as a cortical neurodegenerative disease with infantile onset","year":2014,"lang":"en","type":"article","venue":"Neurogenetics","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":24,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"BC Children's Hospital; B.C. Women's Hospital & Health Centre; Child and Family Research Institute; University of British Columbia","funders":"Canadian Institutes of Health Research","keywords":"Microcephaly; Atrophy; Pathology; Myelin; Medicine; Neuroscience; White matter; Disease; Differential diagnosis; Exome sequencing; Mutation; Biology; Pediatrics; Magnetic resonance imaging; Genetics; Central nervous system","score_opus":0.019945095627185768,"score_gpt":0.25775793002666425,"score_spread":0.23781283439947848,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1968980213","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":[0.98249394,0.0027624248,0.0023109356,0.0007195752,0.000111684174,0.00006393391,0.00079607347,0.00031557705,0.010425819],"genre_scores_gemma":[0.9950787,0.0011149629,0.0015721015,0.00011373303,0.000100037745,0.000027594728,0.00033501655,0.00005398387,0.0016038409],"study_design_codex":"case_report","study_design_gemma":"case_report","domain_scores_codex":[0.99980146,0.000027562714,0.000027143418,0.00004959231,0.000034905293,0.00005926231],"domain_scores_gemma":[0.9994324,0.00015114207,0.00020895373,0.00004101348,0.000045351404,0.00012107589],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00019536504,0.002442498,0.0005648241,0.0017942794,0.0005142353,0.0005579314,0.00068469415,0.0014457585,0.0032788585],"category_scores_gemma":[0.0010646898,0.00041737562,0.0004273297,0.0010237825,0.00078187924,0.0004093774,0.00089274487,0.00071588025,0.00082651514],"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":[0.0005547743,0.00006699125,0.02472324,0.00023933886,0.00007896601,0.9052929,0.00032316125,0.00014381965,0.05608502,0.00065194414,0.0014150941,0.010424736],"study_design_scores_gemma":[0.000033110875,0.00017580016,0.05455872,0.00006320662,0.00016129515,0.9254156,0.00023488053,0.00036378903,0.01509105,0.0006807306,0.0031900445,0.000031864958],"about_ca_topic_score_codex":0.0008834953,"about_ca_topic_score_gemma":0.00080451166,"teacher_disagreement_score":0.0032788585,"about_ca_system_score_codex":0.000325353,"about_ca_system_score_gemma":0.0003504785,"threshold_uncertainty_score":0.010968864},"labels":[],"label_agreement":null},{"id":"W1969621364","doi":"10.1177/0883073813479172","title":"Unilateral Foot Drop as an Initial Presentation of a Brain Tumor in a Child","year":2013,"lang":"en","type":"article","venue":"Journal of Child Neurology","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":7,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Alberta Children's Hospital; University of Calgary","funders":"","keywords":"Foot drop; Foot (prosody); Presentation (obstetrics); Medicine; Peripheral; Central nervous system; Physical medicine and rehabilitation; Psychology; Surgery; Internal medicine","score_opus":0.01941458792561268,"score_gpt":0.2878849170106423,"score_spread":0.2684703290850296,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1969621364","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":[0.98761964,0.0018530285,0.0012491057,0.0014293601,0.00015981386,0.000105608764,0.00044172673,0.00018988685,0.0069518],"genre_scores_gemma":[0.99675614,0.001268401,0.0008524409,0.0003492953,0.00015782773,0.000017539993,0.00013558297,0.000026452464,0.00043634148],"study_design_codex":"case_report","study_design_gemma":"case_report","domain_scores_codex":[0.999622,0.00004132447,0.00004502092,0.000083820596,0.00007265623,0.00013510197],"domain_scores_gemma":[0.9987419,0.00038867054,0.00030316925,0.000047846446,0.00009071594,0.00042779048],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00021065156,0.0012172214,0.0009675172,0.0019608429,0.0012619086,0.0008009868,0.0006342059,0.0019663705,0.0025867783],"category_scores_gemma":[0.0032085353,0.0006534016,0.00050138164,0.0011805085,0.0013840583,0.0013494999,0.00091348233,0.0015336972,0.00063139235],"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":[0.000030210304,0.000027613083,0.02597701,0.000034675417,0.0000062374716,0.97081536,0.00015919158,0.000075244054,0.0012444318,0.00013361649,0.000352135,0.001144221],"study_design_scores_gemma":[0.000007705332,0.00007652769,0.021037314,0.000023612,0.000012597294,0.9776102,0.00016303253,0.00014521184,0.0004546495,0.0000822913,0.00037515903,0.00001174822],"about_ca_topic_score_codex":0.0047180313,"about_ca_topic_score_gemma":0.005951828,"teacher_disagreement_score":0.0047180313,"about_ca_system_score_codex":0.0010119978,"about_ca_system_score_gemma":0.0009747852,"threshold_uncertainty_score":0.009381175},"labels":[],"label_agreement":null},{"id":"W1971220806","doi":"10.1016/s0887-8994(01)00280-6","title":"Late-Onset GM2 gangliosidosis presenting as burning dysesthesias","year":2001,"lang":"en","type":"article","venue":"Pediatric Neurology","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":12,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Toronto; Hospital for Sick Children","funders":"","keywords":"Gangliosidosis; Sandhoff disease; Medicine; Gabapentin; Dermatology; Pathology","score_opus":0.030992272291985687,"score_gpt":0.2680528360581103,"score_spread":0.2370605637661246,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1971220806","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":[0.970471,0.0013017266,0.0024621875,0.00081647094,0.00011338598,0.000105527215,0.000280063,0.00020771111,0.02424187],"genre_scores_gemma":[0.9972096,0.00034804235,0.0005133263,0.0003053111,0.0001000803,0.000015450494,0.000079595804,0.000035441357,0.0013931269],"study_design_codex":"case_report","study_design_gemma":"case_report","domain_scores_codex":[0.999681,0.000026232658,0.000025250903,0.000058520778,0.00004737214,0.00016161556],"domain_scores_gemma":[0.99912816,0.00022696833,0.00025449204,0.000063807485,0.000057780217,0.00026879075],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00030100465,0.0019165146,0.0009848708,0.0011698958,0.0009808756,0.00065723766,0.00077443256,0.0019228945,0.003333217],"category_scores_gemma":[0.0021623743,0.0006633239,0.00043068617,0.00096679473,0.0009772475,0.0009994402,0.0005769039,0.0016872945,0.00082251575],"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":[0.00013271511,0.00006850535,0.011955273,0.000043871485,0.0000111986665,0.9819203,0.0001263885,0.00011271306,0.002853195,0.00028554432,0.00028028135,0.002210044],"study_design_scores_gemma":[0.000028996003,0.00015545677,0.019989263,0.000011620239,0.000019303623,0.97796226,0.000109635235,0.0002495164,0.0009595882,0.00022768548,0.00027627824,0.000010519207],"about_ca_topic_score_codex":0.0028398577,"about_ca_topic_score_gemma":0.0036643627,"teacher_disagreement_score":0.003333217,"about_ca_system_score_codex":0.0007419865,"about_ca_system_score_gemma":0.0006141274,"threshold_uncertainty_score":0.011150718},"labels":[],"label_agreement":null},{"id":"W1971275608","doi":"10.1016/j.ajhg.2013.12.005","title":"Loss of Association of REEP2 with Membranes Leads to Hereditary Spastic Paraplegia","year":2014,"lang":"en","type":"article","venue":"The American Journal of Human Genetics","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":103,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"McGill University; Montreal Neurological Institute and Hospital","funders":"National Institute of Neurological Disorders and Stroke; Canadian Institutes of Health Research","keywords":"Missense mutation; Hereditary spastic paraplegia; Genetics; Biology; Mutation; Splice site mutation; Exome sequencing; Gene; Mutant; Phenotype; Alternative splicing; Exon","score_opus":0.018797895715788958,"score_gpt":0.25905277858989534,"score_spread":0.24025488287410637,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1971275608","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":[0.99566394,0.0003494887,0.0020920052,0.00018856449,0.000054022366,0.00001842114,0.00033034218,0.000098437835,0.0012046803],"genre_scores_gemma":[0.9981717,0.00009757232,0.00077724707,0.000055216704,0.000020786258,0.000009834851,0.00018026575,0.000027662922,0.0006596322],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9996259,0.00010313926,0.00006545123,0.000066189285,0.00008992527,0.000049389826],"domain_scores_gemma":[0.9993143,0.00022148689,0.00026430006,0.000062488856,0.00003086271,0.00010652425],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00023307696,0.00095605385,0.0004086547,0.00074869586,0.00046799224,0.00037828885,0.00068353134,0.0010963765,0.0029955148],"category_scores_gemma":[0.0009920968,0.00031419343,0.00048327408,0.00053311855,0.00049239706,0.00020326993,0.0008238676,0.0007071529,0.000771838],"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":[0.0012989305,0.00025400397,0.009290991,0.00009708386,0.00024466633,0.0469477,0.00020689328,0.0010246518,0.9322283,0.0011799869,0.0007162657,0.006510509],"study_design_scores_gemma":[0.00050063943,0.0008544583,0.14947413,0.00011408374,0.00054906745,0.27139476,0.0004972297,0.013651388,0.5518662,0.0021518932,0.008804337,0.00014186486],"about_ca_topic_score_codex":0.00089864584,"about_ca_topic_score_gemma":0.00088543067,"teacher_disagreement_score":0.0029955148,"about_ca_system_score_codex":0.00029369773,"about_ca_system_score_gemma":0.0002701284,"threshold_uncertainty_score":0.010021031},"labels":[],"label_agreement":null},{"id":"W1971364409","doi":"10.1007/s00401-007-0253-2","title":"EMAP-II antibody detects both proEMAP/p43 and mature EMAP-II molecules","year":2007,"lang":"en","type":"letter","venue":"Acta Neuropathologica","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":3,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Saskatchewan","funders":"","keywords":"Biology","score_opus":0.026150354948203045,"score_gpt":0.2669393690081951,"score_spread":0.24078901405999203,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1971364409","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":[0.1910064,0.0103566665,0.01687238,0.41496283,0.040288337,0.00046734043,0.00065716595,0.0022708916,0.323118],"genre_scores_gemma":[0.71604294,0.0072549414,0.010807403,0.09197351,0.035344392,0.0006182711,0.0007994882,0.00030218632,0.13685685],"study_design_codex":"case_report","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99938726,0.00014317661,0.000067504385,0.00009512493,0.00014197463,0.00016481162],"domain_scores_gemma":[0.9985514,0.0008722972,0.00009751333,0.00018485483,0.00016170461,0.00013227266],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0006491492,0.0018937691,0.0014069122,0.00079157157,0.0015598491,0.0015618295,0.0014213164,0.013146953,0.015778866],"category_scores_gemma":[0.0040969457,0.0007269789,0.00082659896,0.000482306,0.0014340415,0.0022780232,0.00054625253,0.008314474,0.00839857],"study_design_candidate":"bench_or_experimental","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0014492732,0.0005248066,0.007155116,0.00060046674,0.00014991367,0.6537164,0.0003979508,0.0005708398,0.022935841,0.015828658,0.23951913,0.05715158],"study_design_scores_gemma":[0.0007939943,0.0007831444,0.011075031,0.00022659585,0.00023004352,0.66984624,0.00041624924,0.009594824,0.024144521,0.021166613,0.26159558,0.0001272645],"about_ca_topic_score_codex":0.00061420846,"about_ca_topic_score_gemma":0.0007893619,"teacher_disagreement_score":0.015778866,"about_ca_system_score_codex":0.0014851169,"about_ca_system_score_gemma":0.00039915848,"threshold_uncertainty_score":0.052785575},"labels":[],"label_agreement":null},{"id":"W1972218994","doi":"10.1016/j.expneurol.2010.08.002","title":"Regulation of peripheral myelination by Src-like kinases","year":2010,"lang":"en","type":"article","venue":"Experimental Neurology","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":30,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"McGill University","funders":"Canadian Institutes of Health Research; Multiple Sclerosis Society of Canada","keywords":"FYN; Cell biology; Myelin; Kinase; Proto-oncogene tyrosine-protein kinase Src; Myelin basic protein; p38 mitogen-activated protein kinases; MAPK/ERK pathway; Biology; Protein kinase B; Tyrosine kinase; Chemistry; Phosphorylation; Neuroscience; Signal transduction; Central nervous system","score_opus":0.01562920731524558,"score_gpt":0.27024351143513736,"score_spread":0.2546143041198918,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1972218994","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":[0.9898587,0.0046238126,0.0015628027,0.00015715363,0.000029760764,0.0000078030025,0.00008945612,0.000038151236,0.003632423],"genre_scores_gemma":[0.99618715,0.0010482965,0.0007794982,0.000024447743,0.000012783238,0.0000071039867,0.00009088647,0.000007636948,0.0018422449],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9999063,0.000021488147,0.000005908097,0.00001796803,0.000014869365,0.000033357122],"domain_scores_gemma":[0.99990964,0.000019187937,0.000026240334,0.000010067005,0.000012610293,0.000022223843],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00012597363,0.0002711019,0.00015479894,0.00019263428,0.00025055915,0.00026844855,0.00014879464,0.0002053148,0.001232365],"category_scores_gemma":[0.00018475867,0.000078935824,0.00015561424,0.00010266123,0.0002961598,0.00026691853,0.00025519857,0.00034186916,0.00024114289],"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":[0.00059528917,0.00002630142,0.0005112704,0.00004186134,0.000005542509,0.0002561732,0.000039995713,0.000093720664,0.9929842,0.0009995439,0.00011645796,0.0043296027],"study_design_scores_gemma":[0.00009963376,0.0003313836,0.037565827,0.000016320484,0.00002472415,0.0016589815,0.00018093413,0.0020832822,0.9531361,0.0011089809,0.0037813715,0.00001237469],"about_ca_topic_score_codex":0.00042994763,"about_ca_topic_score_gemma":0.00064891105,"teacher_disagreement_score":0.001232365,"about_ca_system_score_codex":0.00035157197,"about_ca_system_score_gemma":0.000108700624,"threshold_uncertainty_score":0.004122615},"labels":[],"label_agreement":null},{"id":"W1973200779","doi":"10.1001/archneur.59.2.281","title":"Spectrum of SPG4 Mutations in a Large Collection of North American Families With Hereditary Spastic Paraplegia","year":2002,"lang":"en","type":"article","venue":"Archives of Neurology","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":78,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Montreal General Hospital","funders":"","keywords":"Hereditary spastic paraplegia; Genetics; Frameshift mutation; Missense mutation; Biology; Nonsense mutation; Mutation; Gene; Exon; Compound heterozygosity; Phenotype","score_opus":0.01637988201397952,"score_gpt":0.22411023312619116,"score_spread":0.20773035111221164,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1973200779","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":[0.9993617,0.000102624326,0.000094538365,0.000023085731,0.0000025703484,0.000010015173,0.00010545491,0.000005678558,0.00029427823],"genre_scores_gemma":[0.99909914,0.00013869235,0.00016278878,0.000050215767,0.000010018922,0.000021632142,0.00032177943,0.0000069976304,0.00018873406],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99946934,0.00011399425,0.000046318033,0.00019193641,0.000112526686,0.000065900545],"domain_scores_gemma":[0.9993218,0.00019002715,0.00015196358,0.0000576245,0.00012582999,0.00015276887],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00033522293,0.0006217791,0.00042700538,0.0015583779,0.0010406863,0.00037568438,0.00038353392,0.00037963782,0.0022110424],"category_scores_gemma":[0.0012829144,0.00029144812,0.00022618493,0.0009823991,0.00056493067,0.0001764491,0.0005639658,0.00022680104,0.0002239709],"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":[0.00016683829,0.000107841006,0.97133183,0.000041792155,0.00013497996,0.011439655,0.0018601323,0.00010496931,0.0073382324,0.000070925,0.00069365563,0.0067092003],"study_design_scores_gemma":[0.000025178459,0.00013638932,0.9687543,0.00002136978,0.00007997349,0.028489599,0.0007673495,0.00017868858,0.00046189484,0.00005138473,0.0010219723,0.0000119312235],"about_ca_topic_score_codex":0.007205158,"about_ca_topic_score_gemma":0.009718765,"teacher_disagreement_score":0.007205158,"about_ca_system_score_codex":0.0004079961,"about_ca_system_score_gemma":0.0003804363,"threshold_uncertainty_score":0.014326453},"labels":[],"label_agreement":null},{"id":"W1973678544","doi":"10.1016/j.nmd.2007.06.438","title":"G.P.18.11 Functional characterization of strumpellin, mutated in hereditary spastic paraplegia","year":2007,"lang":"en","type":"article","venue":"Neuromuscular Disorders","topic":"Hereditary Neurological Disorders","field":"Neuroscience","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":"Université de Montréal; Hôpital Notre-Dame","funders":"","keywords":"Hereditary spastic paraplegia; Mutation; Spasticity; Biology; Gene; Mutant protein; Exon; Spinal muscular atrophy; Gene product; Genetics; Pathology; Medicine; Gene expression; Phenotype","score_opus":0.026230323039871887,"score_gpt":0.2398334715636669,"score_spread":0.21360314852379503,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1973678544","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":[0.9918134,0.0006184024,0.0018397485,0.00035274914,0.00015336546,0.00004737146,0.0012332095,0.00007848553,0.0038632778],"genre_scores_gemma":[0.9924271,0.00024262471,0.0021524876,0.0001753017,0.00006141339,0.00003672719,0.0015416394,0.000050821025,0.0033119125],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99987495,0.000019858266,0.00001916103,0.000032646338,0.000027366981,0.000025924874],"domain_scores_gemma":[0.99962497,0.000096926415,0.000098613375,0.000021986418,0.00005395421,0.00010350276],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00015996347,0.0006882449,0.0002960079,0.00072368863,0.00035761137,0.00028270468,0.0005086913,0.0009594808,0.006306797],"category_scores_gemma":[0.00051789556,0.00012086486,0.00054443505,0.00025728985,0.00040869814,0.00015109105,0.0002538699,0.00052022934,0.001932065],"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":[0.0018534138,0.00027384405,0.00828004,0.00020099372,0.00011240938,0.03510632,0.00022695803,0.0006604449,0.93954813,0.0013520706,0.0014146781,0.010970703],"study_design_scores_gemma":[0.00041113765,0.002167587,0.10282992,0.00013380243,0.0003377863,0.07069318,0.00025290824,0.008299968,0.7909575,0.0013862426,0.022475267,0.00005478148],"about_ca_topic_score_codex":0.0011679484,"about_ca_topic_score_gemma":0.00058881665,"teacher_disagreement_score":0.006306797,"about_ca_system_score_codex":0.00027613578,"about_ca_system_score_gemma":0.00016231598,"threshold_uncertainty_score":0.021098316},"labels":[],"label_agreement":null},{"id":"W1973687042","doi":"10.1016/j.ajhg.2013.05.006","title":"Alteration of Ganglioside Biosynthesis Responsible for Complex Hereditary Spastic Paraplegia","year":2013,"lang":"en","type":"article","venue":"The American Journal of Human Genetics","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":181,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Université de Montréal; McGill University; Montreal Neurological Institute and Hospital","funders":"National Institute of Neurological Disorders and Stroke; Canadian Institutes of Health Research","keywords":"Hereditary spastic paraplegia; Locus (genetics); Genetics; Missense mutation; Biology; Exome sequencing; Exome; Genetic linkage; Disease gene identification; Ataxia; Gene; Mutation; Neuroscience; Phenotype","score_opus":0.06218720409422304,"score_gpt":0.30229610540022883,"score_spread":0.2401089013060058,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1973687042","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":[0.9977283,0.0002135047,0.00094386225,0.0000751878,0.000014703443,0.000017963363,0.000156607,0.000039317692,0.00081052125],"genre_scores_gemma":[0.9990926,0.00007736838,0.000427693,0.000023945859,0.000008301741,0.0000049621626,0.000106383566,0.000011886287,0.00024694382],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99983513,0.000031083102,0.000039062346,0.000035585297,0.000033436212,0.000025585487],"domain_scores_gemma":[0.99963415,0.00008645601,0.00013571548,0.00003234133,0.000035516685,0.00007576748],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00016081824,0.000843078,0.00033300056,0.00093415636,0.0003775425,0.00026900656,0.0003346657,0.00059899525,0.0028782317],"category_scores_gemma":[0.0006200783,0.00020491192,0.00040210635,0.00044620287,0.0007486816,0.00020375542,0.00048011486,0.00035297577,0.0003805943],"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":[0.0023686,0.00012438303,0.018066041,0.00017606682,0.00019327608,0.045637503,0.000261328,0.0009379209,0.9241477,0.0015303212,0.00026092507,0.0062960233],"study_design_scores_gemma":[0.0003704716,0.0009633237,0.14821976,0.00006854748,0.00061038637,0.09363632,0.00034465358,0.0075918436,0.74137807,0.002926827,0.0038125326,0.00007727144],"about_ca_topic_score_codex":0.0015422557,"about_ca_topic_score_gemma":0.00072109676,"teacher_disagreement_score":0.0028782317,"about_ca_system_score_codex":0.00040796204,"about_ca_system_score_gemma":0.00032477998,"threshold_uncertainty_score":0.009628594},"labels":[],"label_agreement":null},{"id":"W1974864196","doi":"10.1016/j.yexcr.2007.03.011","title":"New movements in neurofilament transport, turnover and disease","year":2007,"lang":"en","type":"review","venue":"Experimental Cell Research","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":97,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Wilfrid Laurier University; Université Laval","funders":"","keywords":"Neurofilament; Biology; Axoplasmic transport; Protein subunit; Dynein; Neuroscience; Cell biology; Dynein ATPase; Biochemistry; Immunology; Microtubule; Gene; Immunohistochemistry","score_opus":0.2766047111983867,"score_gpt":0.467630024258892,"score_spread":0.1910253130605053,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1974864196","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":[0.00010807139,0.9980313,0.00029730564,0.0003814343,0.00048047904,0.0000030712831,0.000012591072,0.000009044324,0.00067669095],"genre_scores_gemma":[0.00045660388,0.99759537,0.00037074083,0.00021995213,0.0006074594,0.0000069385183,0.000029341638,0.0000016540195,0.00071196834],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.99976784,0.000030711322,0.00004106961,0.00004217261,0.00009338983,0.000024761848],"domain_scores_gemma":[0.99963284,0.00017502587,0.00004222293,0.000016019812,0.000095715564,0.000038194015],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0011172317,0.0013318413,0.0016482876,0.0020678216,0.00036966047,0.0014588478,0.0014866677,0.0020787339,0.0020581735],"category_scores_gemma":[0.0010179156,0.00041361802,0.0004475865,0.002756381,0.0011983436,0.0023785818,0.0009635423,0.0027024355,0.0014645689],"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":[0.00014094505,0.00007032794,0.00022412413,0.009459234,0.00010186912,0.00046721596,0.00008509649,0.0007295573,0.003325763,0.007376866,0.05861164,0.9194074],"study_design_scores_gemma":[0.00002674977,0.000040922947,0.00064508675,0.0013660421,0.00007628597,0.0013658194,0.00007492527,0.00012463793,0.0005294589,0.0041068885,0.9916243,0.000018845905],"about_ca_topic_score_codex":0.001270887,"about_ca_topic_score_gemma":0.002575766,"teacher_disagreement_score":0.0020787339,"about_ca_system_score_codex":0.0010179261,"about_ca_system_score_gemma":0.0012325399,"threshold_uncertainty_score":0.0073856115},"labels":[],"label_agreement":null},{"id":"W1975014950","doi":"10.1371/journal.pone.0103454","title":"LITAF Mutations Associated with Charcot-Marie-Tooth Disease 1C Show Mislocalization from the Late Endosome/Lysosome to the Mitochondria","year":2014,"lang":"en","type":"article","venue":"PLoS ONE","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":25,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Trent University","funders":"Natural Sciences and Engineering Research Council of Canada","keywords":"Lysosome; Endosome; Mutant; Biology; Cell biology; Golgi apparatus; Mitochondrion; Mutation; Organelle; Genetics; Gene; Biochemistry","score_opus":0.04370534749981472,"score_gpt":0.21728896827859645,"score_spread":0.17358362077878173,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1975014950","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":[0.9960884,0.0007586039,0.0015092605,0.00013849192,0.000036883146,0.00001887459,0.00032870017,0.0000840064,0.0010368624],"genre_scores_gemma":[0.9951912,0.0005445306,0.0018465503,0.00012410819,0.0000121303265,0.000031590913,0.00053871295,0.00005035664,0.001660741],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9997205,0.000038961218,0.000037126636,0.00006762866,0.00009239819,0.000043334254],"domain_scores_gemma":[0.9997631,0.00005832366,0.00009991872,0.000019014797,0.000011715703,0.000048078513],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00018357107,0.00054116524,0.00029798062,0.0004365135,0.00029731376,0.00035945483,0.0003012731,0.00086203794,0.0017068143],"category_scores_gemma":[0.00024083337,0.00023349132,0.00033304247,0.00029587725,0.00051252847,0.00020110674,0.0004571152,0.0006035926,0.0007981562],"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":[0.000087696935,0.000016902002,0.00057918683,0.000035315432,0.0000074108593,0.0008183329,0.000028473769,0.0000389911,0.9976955,0.00005807092,0.000055150962,0.00057904515],"study_design_scores_gemma":[0.00006334757,0.00032104933,0.03875855,0.000028727794,0.000053072275,0.018163031,0.00015342465,0.002042804,0.9357061,0.00016450019,0.004512714,0.000032645254],"about_ca_topic_score_codex":0.001325771,"about_ca_topic_score_gemma":0.0020171902,"teacher_disagreement_score":0.0017068143,"about_ca_system_score_codex":0.00032774862,"about_ca_system_score_gemma":0.00014890151,"threshold_uncertainty_score":0.005709827},"labels":[],"label_agreement":null},{"id":"W1976348742","doi":"10.1097/00131402-200009000-00007","title":"Charcot-Marie-Tooth Disease With Cerebellar Atrophy","year":2000,"lang":"en","type":"article","venue":"Journal of Clinical Neuromuscular Disease","topic":"Hereditary Neurological Disorders","field":"Neuroscience","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":"Atrophy; Tooth disease; Cerebellar ataxia; Medicine; Cerebellum; Magnetic resonance imaging; Polyneuropathy; Ataxia; Pathology; Cerebellar Degeneration; Neuroscience; Disease; Psychiatry; Psychology; Internal medicine; Radiology","score_opus":0.046541905262724476,"score_gpt":0.3187763469911594,"score_spread":0.2722344417284349,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1976348742","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":[0.9740161,0.00569691,0.0008991086,0.0025333767,0.0005786899,0.0001725993,0.00046883203,0.00027205754,0.015362425],"genre_scores_gemma":[0.9930716,0.0013763593,0.00044047972,0.0010826241,0.00064171705,0.000021152866,0.00017005148,0.00002767603,0.003168295],"study_design_codex":"case_report","study_design_gemma":"case_report","domain_scores_codex":[0.99962056,0.000032267813,0.00003624123,0.00010741967,0.000066888904,0.00013670437],"domain_scores_gemma":[0.9990301,0.00017890152,0.0002237086,0.00006379356,0.00007918465,0.0004243418],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.000303719,0.001979197,0.00065890525,0.0011182309,0.0025265743,0.0008284011,0.0006637169,0.002270418,0.0033647795],"category_scores_gemma":[0.0021707523,0.00062524655,0.0004996336,0.0010037749,0.00084796315,0.0010086837,0.0010086471,0.0018584277,0.0010932585],"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":[0.00011721001,0.00009794887,0.01867889,0.00004067233,0.000021529218,0.97650903,0.0002546585,0.000040594212,0.0009828073,0.00010849989,0.0010297591,0.002118568],"study_design_scores_gemma":[0.000041592808,0.00018996929,0.020117357,0.000014198919,0.000024468296,0.97740287,0.00007206311,0.00008018027,0.00030358369,0.00015957934,0.0015790698,0.0000150709],"about_ca_topic_score_codex":0.0062382403,"about_ca_topic_score_gemma":0.010156773,"teacher_disagreement_score":0.0062382403,"about_ca_system_score_codex":0.0006603892,"about_ca_system_score_gemma":0.00062740536,"threshold_uncertainty_score":0.012403905},"labels":[],"label_agreement":null},{"id":"W1976540744","doi":"10.1002/mus.21050","title":"A new <i>MPZ</i> mutation associated with a mild CMT1 phenotype presenting with recurrent nerve compression","year":2008,"lang":"en","type":"article","venue":"Muscle & Nerve","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":24,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Hotel Dieu Hospital","funders":"","keywords":"Phenotype; Mutation; Medicine; Genetics; Biology; Gene","score_opus":0.0531440998170408,"score_gpt":0.25573222638097204,"score_spread":0.20258812656393124,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1976540744","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":[0.9926273,0.0003877241,0.0013423318,0.00054581324,0.00006605314,0.00007329645,0.00022045552,0.00013707193,0.0045999577],"genre_scores_gemma":[0.9974921,0.00015148266,0.00078911905,0.00020564327,0.00009813437,0.000016452566,0.00010947033,0.000026237374,0.0011114791],"study_design_codex":"case_report","study_design_gemma":"case_report","domain_scores_codex":[0.99975234,0.000024880104,0.000022312805,0.00007893138,0.000054206805,0.00006727116],"domain_scores_gemma":[0.9994117,0.00016018996,0.00012557096,0.00002724984,0.00003833078,0.00023692814],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00015816059,0.0014551281,0.00074129814,0.0011279355,0.00089778745,0.0005708315,0.00073095807,0.0019097541,0.0025097916],"category_scores_gemma":[0.0012947134,0.00039739016,0.00049398036,0.0006182975,0.00091368385,0.00042714845,0.0006257112,0.0009869519,0.0006844345],"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":[0.00016504334,0.00010762347,0.011404831,0.000071536146,0.00003960047,0.9548453,0.0004487064,0.00022984362,0.025572984,0.00053607416,0.0011474068,0.00543099],"study_design_scores_gemma":[0.000041173156,0.00022810051,0.022611814,0.000011787715,0.000028398494,0.9728495,0.000056780278,0.0004485926,0.0025382636,0.00018032675,0.0009779101,0.000027275426],"about_ca_topic_score_codex":0.0021070733,"about_ca_topic_score_gemma":0.002218333,"teacher_disagreement_score":0.0025097916,"about_ca_system_score_codex":0.0005442265,"about_ca_system_score_gemma":0.0002976626,"threshold_uncertainty_score":0.008396149},"labels":[],"label_agreement":null},{"id":"W1977780729","doi":"10.1212/01.wnl.0000208415.90685.cd","title":"New <i>HSN2</i> mutation in Japanese patient with hereditary sensory and autonomic neuropathy type 2","year":2006,"lang":"en","type":"article","venue":"Neurology","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":19,"is_retracted":false,"has_abstract":true,"route_ca_aff":false,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":true,"ca_institutions":"","funders":"","keywords":"Frameshift mutation; Sensory neuropathy; Mutation; Medicine; Genetics; Sensory system; Gene; Autonomic neuropathy; Neuroscience; Internal medicine; Biology","score_opus":0.01162173751165431,"score_gpt":0.20678740559638994,"score_spread":0.19516566808473562,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1977780729","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":[0.99723756,0.0002532587,0.0003733164,0.00020055422,0.000035040797,0.000013367711,0.000045294677,0.00002805518,0.0018135618],"genre_scores_gemma":[0.9986162,0.00014975284,0.00037710436,0.000151781,0.000047786252,0.0000069320795,0.000057840232,0.000009537329,0.0005831337],"study_design_codex":"case_report","study_design_gemma":"case_report","domain_scores_codex":[0.99983335,0.000016264305,0.000026214671,0.00005064502,0.000034492205,0.0000390862],"domain_scores_gemma":[0.999788,0.00003182679,0.00003969299,0.000011704426,0.000027072787,0.00010179533],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0001535318,0.0010705144,0.0006021288,0.00060555316,0.0013993984,0.0005018478,0.00039130787,0.0011675351,0.0015645736],"category_scores_gemma":[0.0005470787,0.0005006696,0.0004264387,0.0005412855,0.00067728426,0.00034399488,0.00048243062,0.00048445436,0.00026295485],"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":[0.00026940944,0.00013024548,0.0909782,0.00012194854,0.00011624876,0.8464493,0.0025385509,0.00026990165,0.051711038,0.00038458782,0.0012120778,0.0058185398],"study_design_scores_gemma":[0.00016039317,0.0003599513,0.14570631,0.000044384935,0.00025994217,0.841363,0.0010014994,0.0009848886,0.0058380356,0.00040427572,0.003808132,0.0000690944],"about_ca_topic_score_codex":0.006920964,"about_ca_topic_score_gemma":0.012281861,"teacher_disagreement_score":0.006920964,"about_ca_system_score_codex":0.0005036072,"about_ca_system_score_gemma":0.00037689126,"threshold_uncertainty_score":0.013761342},"labels":[],"label_agreement":null},{"id":"W1977781304","doi":"10.4021/wjon278w","title":"Increased Incidence of Tumors With the IKBKAP Gene Mutation? A Case Report and Review of the Literature","year":2011,"lang":"en","type":"article","venue":"World Journal of Oncology","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":3,"is_retracted":false,"has_abstract":true,"route_ca_aff":false,"route_ca_fund":false,"route_ca_venue":true,"route_about_ca":false,"ca_institutions":"","funders":"National Institutes of Health; Dysautonomia Foundation","keywords":"Familial dysautonomia; Medicine; Incidence (geometry); Population; Mutation; Gene; Dysautonomia; Pathology; Genetics; Internal medicine; Biology; Disease; Environmental health","score_opus":0.03163598464062798,"score_gpt":0.29276932158316066,"score_spread":0.26113333694253266,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1977781304","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":[0.5482344,0.4230609,0.0034527935,0.003185539,0.0017295213,0.00009983055,0.0006076816,0.00048352886,0.019145785],"genre_scores_gemma":[0.8293321,0.15861726,0.0016312925,0.0019892743,0.0038769902,0.000049973136,0.00042046883,0.000067690555,0.004015035],"study_design_codex":"case_report","study_design_gemma":"case_report","domain_scores_codex":[0.99947244,0.000060961658,0.00014144504,0.00013421947,0.00009513975,0.000095749325],"domain_scores_gemma":[0.99910456,0.0003164941,0.00031959967,0.00007023955,0.00010437882,0.00008478868],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00026280322,0.00072474463,0.0010745518,0.0027329025,0.00053910026,0.0012526261,0.0010877562,0.0022978757,0.0029166942],"category_scores_gemma":[0.0011794436,0.0004623461,0.0004892337,0.0024184634,0.0009188539,0.0015043132,0.00048304285,0.00060503744,0.0019360597],"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":[0.0000931102,0.00007012733,0.023739643,0.0011472491,0.00010707754,0.93227947,0.00033348895,0.00013851223,0.0023531541,0.00015928267,0.004180101,0.0353988],"study_design_scores_gemma":[0.000005882189,0.000035168687,0.008528832,0.00010513639,0.000076965065,0.9851008,0.000157438,0.00006493512,0.0003117032,0.00007815218,0.0055201724,0.000014918708],"about_ca_topic_score_codex":0.00082469115,"about_ca_topic_score_gemma":0.00082480273,"teacher_disagreement_score":0.0029166942,"about_ca_system_score_codex":0.0003245039,"about_ca_system_score_gemma":0.00033401864,"threshold_uncertainty_score":0.00975734},"labels":[],"label_agreement":null},{"id":"W1979686511","doi":"10.1111/j.1600-0404.2008.01134.x","title":"Poor tolerability of high dose ascorbic acid in a population of genetically confirmed adult Charcot-Marie-Tooth 1A patients","year":2008,"lang":"en","type":"article","venue":"Acta Neurologica Scandinavica","topic":"Hereditary Neurological Disorders","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":"University of Calgary","funders":"","keywords":"Tolerability; Medicine; Adverse effect; Cohort; Ascorbic acid; Internal medicine; Population; Gastroenterology; Clinical trial; Surgery; Biology","score_opus":0.024918696795268064,"score_gpt":0.24282119536358654,"score_spread":0.21790249856831848,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1979686511","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":[0.99949217,0.00018962141,0.00004417565,0.000019502024,0.0000020871428,0.0000063503862,0.000038032176,0.0000030265082,0.00020489182],"genre_scores_gemma":[0.99974865,0.00006158273,0.000036112066,0.000030040344,0.000005233239,0.000006370318,0.00006482937,9.668368e-7,0.00004619121],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99972266,0.00007299311,0.00003309802,0.000073755415,0.00006800106,0.00002934048],"domain_scores_gemma":[0.9987484,0.00036447207,0.00048371142,0.00006887805,0.00013672376,0.00019780119],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0006400366,0.00020736067,0.00039797288,0.00028425493,0.00040629003,0.00045432476,0.00015695796,0.0003473655,0.001128504],"category_scores_gemma":[0.0016465051,0.00007795023,0.0002581132,0.00021709998,0.00024639606,0.00023542566,0.00012720244,0.00028634584,0.00019887077],"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":[0.0049817907,0.00048234747,0.9539919,0.00006613087,0.00018772432,0.0024712365,0.00055922347,0.00026386086,0.014414198,0.000048249585,0.0003257734,0.02220752],"study_design_scores_gemma":[0.00016845755,0.009179122,0.98159385,0.000020290707,0.00013646572,0.0065482096,0.00035878265,0.0003637469,0.0010203626,0.00006345955,0.0005324509,0.000014795953],"about_ca_topic_score_codex":0.0008233543,"about_ca_topic_score_gemma":0.0006206027,"teacher_disagreement_score":0.001128504,"about_ca_system_score_codex":0.00026954288,"about_ca_system_score_gemma":0.00017797358,"threshold_uncertainty_score":0.0037751794},"labels":[],"label_agreement":null},{"id":"W1980615395","doi":"10.1111/j.1399-0004.2008.00962_3.x","title":"CMT4J: Charcot–Marie–Tooth disorder caused by mutations in <i>FIG4</i>","year":2008,"lang":"en","type":"letter","venue":"Clinical Genetics","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":4,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of British Columbia","funders":"","keywords":"Neurodegeneration; Mutation; Biology; Genetics; Medicine; Pathology; Gene; Disease","score_opus":0.10338236949106804,"score_gpt":0.34525451814046026,"score_spread":0.24187214864939222,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1980615395","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":[0.13711758,0.009992648,0.00392094,0.7052667,0.037463777,0.0003509086,0.001660845,0.0013463368,0.10288019],"genre_scores_gemma":[0.5894632,0.008754312,0.0046207034,0.21391955,0.06448249,0.00026095388,0.0009700505,0.00042325133,0.11710548],"study_design_codex":"case_report","study_design_gemma":"case_report","domain_scores_codex":[0.99961406,0.000075244556,0.00003643874,0.00009469354,0.00008065944,0.000098911434],"domain_scores_gemma":[0.99940884,0.00028954336,0.000055233548,0.0000253208,0.00008672453,0.00013431876],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0005210658,0.0014365374,0.0011477491,0.0005883446,0.0015937703,0.00097302033,0.0011458249,0.010523782,0.0065076416],"category_scores_gemma":[0.0016350945,0.00036400207,0.00077062397,0.00037469735,0.0016358964,0.00094542897,0.00045658607,0.005788377,0.0024573982],"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":[0.0011291495,0.00018938145,0.0061816163,0.00020033366,0.00012358736,0.63473463,0.0002170117,0.00033881265,0.00849762,0.004019216,0.32688043,0.017488208],"study_design_scores_gemma":[0.0015776426,0.0011617314,0.05571939,0.00048656279,0.0004104497,0.65454435,0.0005399259,0.006362419,0.011204816,0.011393108,0.2563495,0.00025016317],"about_ca_topic_score_codex":0.003721521,"about_ca_topic_score_gemma":0.004250121,"teacher_disagreement_score":0.010523782,"about_ca_system_score_codex":0.0019617297,"about_ca_system_score_gemma":0.00055576937,"threshold_uncertainty_score":0.02177018},"labels":[],"label_agreement":null},{"id":"W1982369903","doi":"10.1002/mus.1067","title":"Severe infantile axonal neuropathy with respiratory failure","year":2001,"lang":"en","type":"article","venue":"Muscle & Nerve","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":34,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"London Health Sciences Centre; Alberta Children's Hospital","funders":"","keywords":"Medicine; Respiratory failure; Peripheral neuropathy; Pediatrics; Respiratory system; Physical medicine and rehabilitation; Neuroscience; Internal medicine; Psychology; Endocrinology","score_opus":0.028741259128969455,"score_gpt":0.23475496604760512,"score_spread":0.20601370691863566,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1982369903","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":[0.9948549,0.00074061,0.0010801946,0.00017834493,0.000038117683,0.000037123278,0.000059342747,0.00007520846,0.002936094],"genre_scores_gemma":[0.9983321,0.0002699633,0.00046024678,0.00017082956,0.00005659083,0.000013672405,0.00004778774,0.000009697083,0.0006391247],"study_design_codex":"case_report","study_design_gemma":"case_report","domain_scores_codex":[0.99952376,0.00007477916,0.000043071042,0.00009037938,0.000082859464,0.00018521314],"domain_scores_gemma":[0.9993351,0.00013321574,0.00021850932,0.00005577732,0.000041075014,0.00021628555],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00033887877,0.0016544848,0.0006830833,0.0006855819,0.00089659245,0.00041779262,0.0004996886,0.0012147792,0.0014945093],"category_scores_gemma":[0.0018674539,0.00047055565,0.00046742006,0.0003680654,0.00065327086,0.00037735235,0.00095166115,0.0011370168,0.0003144065],"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":[0.00014182112,0.00010219202,0.07660838,0.00008350379,0.000048534283,0.90884376,0.0005767655,0.0003534851,0.0032732289,0.00035245455,0.0006195993,0.008996338],"study_design_scores_gemma":[0.000017301316,0.0006474161,0.06603911,0.00001582799,0.00003073438,0.9311629,0.00015083044,0.00030369346,0.0008368676,0.00011536207,0.0006631795,0.000016779377],"about_ca_topic_score_codex":0.0013886503,"about_ca_topic_score_gemma":0.0022839492,"teacher_disagreement_score":0.0016544848,"about_ca_system_score_codex":0.00048555623,"about_ca_system_score_gemma":0.00026921747,"threshold_uncertainty_score":0.004999578},"labels":[],"label_agreement":null},{"id":"W1984864188","doi":"10.1002/jnr.20425","title":"An 8.5-kb segment of the PMP22 promoter responds to loss of axon signals during Wallerian degeneration, but does not respond to specific axonal signals during nerve regeneration","year":2005,"lang":"en","type":"article","venue":"Journal of Neuroscience Research","topic":"Hereditary Neurological Disorders","field":"Neuroscience","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":"Royal Victoria Hospital; Montreal Neurological Institute and Hospital; McGill University","funders":"McGill University","keywords":"Wallerian degeneration; Biology; Transgene; Remyelination; Axon; Myelin; Schwann cell; Cell biology; Neuroscience; Gene; Molecular biology; Genetics; Central nervous system","score_opus":0.11112170647674385,"score_gpt":0.36340850851531625,"score_spread":0.2522868020385724,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1984864188","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":[0.9975802,0.00030792985,0.0014429046,0.000023046467,0.0000065335444,0.000007979859,0.000121097124,0.000037971047,0.0004722834],"genre_scores_gemma":[0.99266267,0.0003274501,0.0027496112,0.000029363986,0.0000051135394,0.000031638203,0.0011416173,0.000035807316,0.0030168232],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99990654,0.000011298457,0.00000787885,0.000027990603,0.000023476812,0.00002285616],"domain_scores_gemma":[0.99989784,0.000019499763,0.000035930567,0.00000922664,0.000009279676,0.000028202494],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00007905718,0.00034740393,0.00013108629,0.00014250672,0.00006368675,0.00016027951,0.00015132074,0.00017361845,0.00091036485],"category_scores_gemma":[0.00012918179,0.00013873915,0.00013690325,0.00007714655,0.000201408,0.00010037613,0.00019124047,0.00041916754,0.0004132621],"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":[0.000026876494,0.000007755075,0.00010455143,0.0000071590684,9.243673e-7,0.000028627455,0.000005053268,0.000023722043,0.99951875,0.000018125653,0.0000041344306,0.00025415485],"study_design_scores_gemma":[0.000015746316,0.00017942765,0.0089594815,0.000014265417,0.00001609259,0.0006571163,0.000028744367,0.0009121352,0.98755324,0.000033652774,0.0016255506,0.0000044599333],"about_ca_topic_score_codex":0.00038939685,"about_ca_topic_score_gemma":0.00067060837,"teacher_disagreement_score":0.00091036485,"about_ca_system_score_codex":0.00021438103,"about_ca_system_score_gemma":0.00017370108,"threshold_uncertainty_score":0.0030454993},"labels":[],"label_agreement":null},{"id":"W1985360445","doi":"10.1007/s00415-011-5910-7","title":"Mutation screening of mitofusin 2 in Charcot-Marie-Tooth disease type 2","year":2011,"lang":"en","type":"article","venue":"Journal of Neurology","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":39,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Kingston General Hospital","funders":"National Institute of Neurological Disorders and Stroke","keywords":"Neurology; Neuroradiology; Tooth disease; Mutation; Medicine; Disease; Degenerative disease; Genetics; Pathology; Biology; Psychiatry; Gene","score_opus":0.08783964096900383,"score_gpt":0.2780336062064913,"score_spread":0.1901939652374875,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1985360445","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":[0.9969355,0.00060657784,0.00074666616,0.00015701489,0.000053181546,0.00002924964,0.00021084277,0.00004259228,0.0012183964],"genre_scores_gemma":[0.9985253,0.00012697528,0.00066916796,0.00006514621,0.00002029244,0.000008878191,0.00012262241,0.000008700131,0.0004529415],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.99952006,0.000053932243,0.00007392988,0.00011628862,0.00015704018,0.000078789264],"domain_scores_gemma":[0.99942064,0.00023933662,0.00006277811,0.000017105898,0.00010194977,0.00015819048],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00050582597,0.0010087466,0.00050156185,0.0027083317,0.00090352556,0.00059089065,0.00063749193,0.001618965,0.0015705049],"category_scores_gemma":[0.0018894739,0.00028074338,0.0005856089,0.000584512,0.00046139865,0.00029709897,0.00046743697,0.00034369904,0.0003092737],"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":[0.001772516,0.0002727292,0.19008046,0.00015365669,0.00022284669,0.25706324,0.0013090295,0.00066749816,0.53443444,0.0005110341,0.0010827385,0.01242979],"study_design_scores_gemma":[0.00020165945,0.0015146566,0.32999444,0.00012637266,0.00057806936,0.42290732,0.0012257929,0.008289317,0.22808787,0.0007285649,0.0062313513,0.000114572955],"about_ca_topic_score_codex":0.0026955686,"about_ca_topic_score_gemma":0.0027316723,"teacher_disagreement_score":0.0027083317,"about_ca_system_score_codex":0.00038307827,"about_ca_system_score_gemma":0.00025643638,"threshold_uncertainty_score":0.005359769},"labels":[],"label_agreement":null},{"id":"W1986277022","doi":"10.1212/wnl.0b013e318217e77d","title":"Simultaneous <i>MFN2</i> and <i>GDAP1</i> mutations cause major mitochondrial defects in a patient with CMT","year":2011,"lang":"en","type":"article","venue":"Neurology","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":38,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of British Columbia Hospital","funders":"","keywords":"MFN2; Pes cavus; Medicine; Neurology; Mitochondrial DNA; Neuroscience; Biology; Internal medicine; Genetics; Gene; mitochondrial fusion","score_opus":0.021747988887924095,"score_gpt":0.22257700534347147,"score_spread":0.20082901645554738,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1986277022","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":[0.99628025,0.00033398217,0.0005626087,0.0003910442,0.00003802173,0.000035814777,0.00014578806,0.000034004865,0.0021783973],"genre_scores_gemma":[0.9982173,0.00015001485,0.00062102504,0.00019826827,0.00006300433,0.000012517002,0.00009603312,0.0000138266,0.00062810525],"study_design_codex":"case_report","study_design_gemma":"case_report","domain_scores_codex":[0.9996586,0.000031123116,0.000043133423,0.00013079337,0.000073544754,0.00006278803],"domain_scores_gemma":[0.9996896,0.0000923254,0.000048225415,0.000014716282,0.00001980632,0.00013540097],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00022190079,0.0014242396,0.00077513687,0.001039987,0.0012781821,0.00052606023,0.0005722282,0.0018210956,0.002149078],"category_scores_gemma":[0.0010565983,0.00045441554,0.00043573917,0.0005051163,0.0010485067,0.00053279044,0.00068062794,0.0011931055,0.0005374413],"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":[0.00045362,0.0002598549,0.03163903,0.00006993459,0.000047479545,0.88693845,0.0013693135,0.00033817597,0.07332247,0.00044464917,0.00057927275,0.004537775],"study_design_scores_gemma":[0.00007255596,0.0007011515,0.05120194,0.0000273297,0.000080956765,0.9319295,0.00028899973,0.00066389865,0.013233866,0.00030690397,0.0014483348,0.00004455237],"about_ca_topic_score_codex":0.0018449804,"about_ca_topic_score_gemma":0.0028900523,"teacher_disagreement_score":0.002149078,"about_ca_system_score_codex":0.000614421,"about_ca_system_score_gemma":0.0003686037,"threshold_uncertainty_score":0.007189393},"labels":[],"label_agreement":null},{"id":"W1986801602","doi":"10.1002/mds.21005","title":"Novel <i>SPG6</i> mutation p.A100T in a Japanese family with autosomal dominant form of hereditary spastic paraplegia","year":2006,"lang":"en","type":"article","venue":"Movement Disorders","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":20,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University Health Network; University of Toronto","funders":"","keywords":"Hereditary spastic paraplegia; Paraplegia; Mutation; Spastic; Genetics; Allele; Medicine; Autosomal recessive inheritance; Biology; Gene; Phenotype; Physical therapy; Spinal cord; Cerebral palsy; Psychiatry","score_opus":0.012679596020365358,"score_gpt":0.218128676561311,"score_spread":0.20544908054094563,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1986801602","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":[0.9973258,0.00017786611,0.0011708194,0.00020874033,0.000031007312,0.000016876478,0.000047838013,0.00004353716,0.0009775352],"genre_scores_gemma":[0.9987232,0.00010188893,0.00061506865,0.000103468876,0.000034876397,0.0000065149206,0.000042532196,0.000011577984,0.00036088345],"study_design_codex":"case_report","study_design_gemma":"observational","domain_scores_codex":[0.9998554,0.000018842742,0.000018109242,0.000054071737,0.000030690324,0.000022962415],"domain_scores_gemma":[0.99967396,0.00007310785,0.00007505154,0.000021703416,0.000031938056,0.00012421342],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00017523638,0.0013041979,0.0004775565,0.00067187013,0.00096373045,0.00033720557,0.00046465534,0.0010827415,0.0013513538],"category_scores_gemma":[0.00054339843,0.00041503875,0.00052668614,0.00050498126,0.0008276524,0.00028399355,0.00060517405,0.0006904767,0.000326593],"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":[0.00014165594,0.00008530657,0.029887116,0.00007944042,0.00007748016,0.8944719,0.0012022895,0.00019643006,0.06829882,0.00026436336,0.00044040772,0.004854836],"study_design_scores_gemma":[0.00008396807,0.00036506398,0.071801595,0.000026520436,0.00021025048,0.915909,0.0003635579,0.0010346621,0.008466604,0.0003842508,0.0013110714,0.00004338983],"about_ca_topic_score_codex":0.0025794022,"about_ca_topic_score_gemma":0.0034775764,"teacher_disagreement_score":0.0025794022,"about_ca_system_score_codex":0.00023797674,"about_ca_system_score_gemma":0.00024892902,"threshold_uncertainty_score":0.0051287413},"labels":[],"label_agreement":null},{"id":"W1988314408","doi":"10.1016/j.yexcr.2014.02.021","title":"Molecular aspects of hereditary spastic paraplegia","year":2014,"lang":"en","type":"review","venue":"Experimental Cell Research","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":57,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"McGill University; Université de Montréal; Montreal Neurological Institute and Hospital","funders":"Canadian Institutes of Health Research","keywords":"Hereditary spastic paraplegia; Biology; Disease; Mendelian inheritance; Spasticity; Genetics; Identification (biology); Genetic heterogeneity; Gene; Bioinformatics; Neuroscience; Phenotype; Medicine; Pathology","score_opus":0.18200168711470108,"score_gpt":0.44237971522878566,"score_spread":0.2603780281140846,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1988314408","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":[0.00008527208,0.9985398,0.00013281047,0.00022029142,0.0002423044,0.0000029748433,0.000015898617,0.000005224533,0.0007554068],"genre_scores_gemma":[0.00049839396,0.9984426,0.00015205478,0.00015147714,0.0002639315,0.0000031925788,0.000030640236,9.559421e-7,0.00045669102],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.9998398,0.000023599308,0.00002859258,0.000027234852,0.000058999314,0.000021693315],"domain_scores_gemma":[0.99978477,0.000099068726,0.000029437992,0.000008050301,0.000051065603,0.000027734011],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0005686155,0.0010773881,0.0014371071,0.0022114338,0.00026261862,0.0010440522,0.0011486833,0.0012166701,0.002556913],"category_scores_gemma":[0.0005967197,0.00031306676,0.00038379105,0.0021912886,0.0008567178,0.0013736946,0.0009022717,0.0017119112,0.0013876158],"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":[0.00012783596,0.00005975858,0.00022349483,0.015418997,0.00009965686,0.00066066114,0.00005725733,0.0005972075,0.0031852843,0.005639107,0.04627462,0.9276561],"study_design_scores_gemma":[0.000023560784,0.00003820884,0.0008008414,0.0025419928,0.00013082207,0.0021871268,0.00006707971,0.0000930918,0.00053412287,0.003390531,0.99017227,0.000020322079],"about_ca_topic_score_codex":0.0011696646,"about_ca_topic_score_gemma":0.002276282,"teacher_disagreement_score":0.002556913,"about_ca_system_score_codex":0.0008399248,"about_ca_system_score_gemma":0.0011576103,"threshold_uncertainty_score":0.008553743},"labels":[],"label_agreement":null},{"id":"W1988750456","doi":"10.1002/ajh.1149","title":"Gelatinous transformation of bone marrow from a starch‐free diet","year":2001,"lang":"en","type":"article","venue":"American Journal of Hematology","topic":"Hereditary Neurological Disorders","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":"University of Toronto; Mount Sinai Hospital","funders":"","keywords":"Anorexia nervosa; Bone marrow; Wasting; Complication; Atrophy; Medicine; Hypoplasia; Internal medicine; Hematology; Endocrinology; Pathology; Surgery; Gastroenterology; Physiology; Eating disorders","score_opus":0.020442679851243654,"score_gpt":0.2557655206603293,"score_spread":0.23532284080908566,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1988750456","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":[0.99382704,0.00044911998,0.0019132606,0.000096323995,0.000021696691,0.000042878568,0.000041993077,0.000067478555,0.0035401739],"genre_scores_gemma":[0.9983139,0.00024383498,0.00045708028,0.000056242938,0.0000073855,0.000009536943,0.00005922546,0.000010050757,0.00084280415],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9999385,0.000010829449,0.0000068182676,0.000010683904,0.000016489095,0.000016704877],"domain_scores_gemma":[0.9998958,0.000022597802,0.000027251239,0.000021972332,0.0000052597893,0.000027025917],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0000673518,0.00030123722,0.00012948134,0.00034033964,0.00023926469,0.00019850778,0.00015438414,0.00030486606,0.0007397918],"category_scores_gemma":[0.0003387517,0.0001192252,0.0001753589,0.00013550851,0.0004030387,0.0001344609,0.00033799862,0.00047459977,0.00025211196],"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":[0.0015320133,0.00026107702,0.017810125,0.00012745816,0.000056135286,0.4015263,0.00065045553,0.00039307176,0.55007195,0.0019901404,0.00041582805,0.025165467],"study_design_scores_gemma":[0.00025941682,0.0012515588,0.04863154,0.000026315622,0.00008256673,0.7588074,0.00024997158,0.0013507253,0.18045315,0.0012258681,0.0076324283,0.000028987655],"about_ca_topic_score_codex":0.00035341046,"about_ca_topic_score_gemma":0.00044297962,"teacher_disagreement_score":0.0007397918,"about_ca_system_score_codex":0.00015359608,"about_ca_system_score_gemma":0.0001243319,"threshold_uncertainty_score":0.0024748445},"labels":[],"label_agreement":null},{"id":"W1989551700","doi":"10.1002/humu.20508","title":"Linkage to a known gene but no mutation identified: comprehensive reanalysis ofSPG4 HSP pedigrees reveals large deletions as the sole cause","year":2007,"lang":"en","type":"letter","venue":"Human Mutation","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":10,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"McGill University; Hôpital Notre-Dame","funders":"","keywords":"Pedigree chart; Library science; Genetics; Biology; Gene","score_opus":0.06873413592712121,"score_gpt":0.331773143476188,"score_spread":0.26303900754906684,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1989551700","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":[0.5709413,0.003534357,0.0046677548,0.3701434,0.010433785,0.00026808583,0.0010854102,0.0006372898,0.038288638],"genre_scores_gemma":[0.92492425,0.0017788459,0.0030553194,0.040457863,0.011908726,0.00010112922,0.00035802307,0.00016914634,0.017246827],"study_design_codex":"case_report","study_design_gemma":"observational","domain_scores_codex":[0.99945825,0.00011365268,0.00006709347,0.00014567946,0.00010597636,0.0001094174],"domain_scores_gemma":[0.9978188,0.0012248515,0.0001285089,0.0001343379,0.0002532377,0.00044023155],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0005652689,0.0012832278,0.0013648605,0.0009382595,0.0015870022,0.0010075998,0.0015979703,0.009590773,0.005752949],"category_scores_gemma":[0.00456061,0.0004413884,0.00066119403,0.0005751783,0.0015371016,0.00089409115,0.0003314909,0.0051444992,0.0012040284],"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":[0.00068099494,0.00016218484,0.016716205,0.00018121433,0.00009898836,0.9113838,0.0005557414,0.0005968322,0.0046025175,0.0018260268,0.05126431,0.011931159],"study_design_scores_gemma":[0.00054564845,0.0006804571,0.041551802,0.00014758475,0.00029107748,0.88736385,0.0008020337,0.007687183,0.0080543775,0.0071901698,0.04555092,0.00013496913],"about_ca_topic_score_codex":0.00418224,"about_ca_topic_score_gemma":0.004084798,"teacher_disagreement_score":0.009590773,"about_ca_system_score_codex":0.0012274764,"about_ca_system_score_gemma":0.00086832634,"threshold_uncertainty_score":0.019245565},"labels":[],"label_agreement":null},{"id":"W1991048512","doi":"10.1371/journal.pone.0030003","title":"Accumulation of Endogenous LITAF in Aggresomes","year":2012,"lang":"en","type":"article","venue":"PLoS ONE","topic":"Hereditary Neurological Disorders","field":"Neuroscience","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":"Trent University","funders":"Natural Sciences and Engineering Research Council of Canada","keywords":"Aggresome; Endosome; Transfection; Biology; Intracellular; HEK 293 cells; Chemistry; Computational biology; Cell biology; Genetics; Cell culture; Gene; Ubiquitin","score_opus":0.4113129638081507,"score_gpt":0.31582038870201723,"score_spread":0.09549257510613346,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1991048512","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":[0.9944502,0.00048160908,0.0035298974,0.000048308404,0.000012276112,0.000013398662,0.00031872757,0.00005751375,0.0010880758],"genre_scores_gemma":[0.9916088,0.00033497575,0.003894882,0.00005097407,0.0000059417866,0.000021399275,0.0008559095,0.00003373167,0.0031934725],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99987113,0.0000134436195,0.0000141981545,0.00003573428,0.000042843814,0.000022636672],"domain_scores_gemma":[0.9998344,0.00002547794,0.000040364685,0.000023548058,0.000027728274,0.00004837576],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00011596125,0.00022126148,0.00024097579,0.00030636427,0.00028749503,0.00032850628,0.00017697887,0.00024563467,0.00082601246],"category_scores_gemma":[0.000096235664,0.00014838588,0.00022153782,0.00015605123,0.00022186547,0.00021286319,0.00030519,0.0003670774,0.00043161836],"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":[0.000019719186,0.000004649498,0.00017514598,0.000012971487,0.000003609104,0.00009989619,0.000014562331,0.0000125649885,0.99937004,0.00006505349,0.00001305974,0.00020871467],"study_design_scores_gemma":[0.0000071307686,0.000084001396,0.011064503,0.000008014785,0.00001517731,0.0015933537,0.000061697676,0.00074432365,0.9840852,0.00013740231,0.002191501,0.000007702423],"about_ca_topic_score_codex":0.0006165316,"about_ca_topic_score_gemma":0.0011317041,"teacher_disagreement_score":0.00082601246,"about_ca_system_score_codex":0.0004023567,"about_ca_system_score_gemma":0.0001769674,"threshold_uncertainty_score":0.002919376},"labels":[],"label_agreement":null},{"id":"W1991579714","doi":"10.1016/j.nmd.2008.04.001","title":"Founder SH3TC2 mutations are responsible for a CMT4C French-Canadians cluster","year":2008,"lang":"en","type":"article","venue":"Neuromuscular Disorders","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":42,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Hôpital de l'Enfant-Jésus; Université Laval; Cégep de Jonquière; Centre Hospitalier Universitaire Sainte-Justine; Hôpital Notre-Dame; Centre Hospitalier de l’Université de Montréal","funders":"Fonds de Recherche du Québec - Santé","keywords":"Genetics; Haplotype; Locus (genetics); Biology; Mutation; Genetic heterogeneity; Founder effect; Cluster (spacecraft); Gene; Phenotype; Allele","score_opus":0.04223080523847606,"score_gpt":0.2572208971525123,"score_spread":0.21499009191403623,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1991579714","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":[0.9764814,0.00080340274,0.000978612,0.0021527451,0.00025537208,0.00008343417,0.0020914606,0.00010995513,0.017043587],"genre_scores_gemma":[0.99353844,0.00024187284,0.0011155742,0.0003111475,0.00013406544,0.000014342106,0.00049464696,0.000041234205,0.00410871],"study_design_codex":"case_report","study_design_gemma":"observational","domain_scores_codex":[0.99950325,0.000031959076,0.000039245013,0.000107392516,0.0001504217,0.00016777698],"domain_scores_gemma":[0.9991491,0.00019788546,0.00015766923,0.00003146502,0.00019620697,0.0002676933],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0002547032,0.002008596,0.00059797225,0.002279478,0.00435436,0.0008599771,0.0013413766,0.0024805558,0.014219598],"category_scores_gemma":[0.0015819473,0.00033321997,0.0010870994,0.002178871,0.001260071,0.00028938454,0.0008771744,0.0010130642,0.0008210615],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":true,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0016256166,0.00020097043,0.15461081,0.00025743834,0.00048963475,0.7290979,0.0040563997,0.001827946,0.067668654,0.004704095,0.015035647,0.020424971],"study_design_scores_gemma":[0.00039873816,0.00027212437,0.34131914,0.00028886631,0.0007983228,0.595777,0.0035813695,0.0037171731,0.01604747,0.0012824963,0.036304813,0.00021258614],"about_ca_topic_score_codex":0.43202782,"about_ca_topic_score_gemma":0.40955773,"teacher_disagreement_score":0.5679722,"about_ca_system_score_codex":0.00329605,"about_ca_system_score_gemma":0.0048958086,"threshold_uncertainty_score":0.85902625},"labels":[],"label_agreement":null},{"id":"W1992620796","doi":"10.1089/jayao.2013.0009","title":"Delayed Diagnosis of Metastatic Ewing Sarcoma Masked by Charcot-Marie-Tooth Disease","year":2013,"lang":"en","type":"article","venue":"Journal of Adolescent and Young Adult Oncology","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":2,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University Health Network; Hospital for Sick Children; University of Toronto","funders":"","keywords":"Medicine; Sarcoma; Tooth disease; Disease; Ewing's sarcoma; Gluteal region; Metastasis; Surgery; Pediatrics; Pathology; Internal medicine; Cancer","score_opus":0.025063350564060137,"score_gpt":0.2758964910852701,"score_spread":0.25083314052121,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1992620796","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":[0.9870964,0.002053652,0.001122156,0.0026172115,0.00023288319,0.000041321797,0.00010715605,0.000067331515,0.006661852],"genre_scores_gemma":[0.99765426,0.0006794854,0.00051973615,0.00031336988,0.00020891623,0.0000053168924,0.000028475579,0.000008004561,0.00058234396],"study_design_codex":"case_report","study_design_gemma":"case_report","domain_scores_codex":[0.99967897,0.000037540904,0.00003327158,0.00006998477,0.00005526329,0.00012502339],"domain_scores_gemma":[0.99864453,0.00053833914,0.0002684386,0.000051742027,0.00009909201,0.00039787896],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00025863273,0.0009984242,0.0007041217,0.0011129482,0.0015401454,0.00089163374,0.00074839836,0.0027184996,0.0018201735],"category_scores_gemma":[0.0040113255,0.00056159165,0.0004760004,0.00056603906,0.00093981676,0.0014207357,0.00084102,0.0023786398,0.0005454937],"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":[0.000027552142,0.000014971356,0.005816818,0.000010115375,0.0000021372127,0.99252784,0.000109551744,0.00004278125,0.0005014717,0.00009986983,0.00010515964,0.0007416955],"study_design_scores_gemma":[0.0000063848247,0.00004924289,0.0034441762,0.000012064199,0.000006444175,0.9953603,0.00011739488,0.00019945978,0.00037903123,0.00015668757,0.0002621687,0.0000065506524],"about_ca_topic_score_codex":0.003104206,"about_ca_topic_score_gemma":0.004373609,"teacher_disagreement_score":0.003104206,"about_ca_system_score_codex":0.0010605429,"about_ca_system_score_gemma":0.0008425408,"threshold_uncertainty_score":0.0076948404},"labels":[],"label_agreement":null},{"id":"W1995784041","doi":"10.1093/hmg/ddl011","title":"Aggregate formation and phosphorylation of neurofilament-L Pro22 Charcot–Marie–Tooth disease mutants","year":2006,"lang":"en","type":"article","venue":"Human Molecular Genetics","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":86,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Centre hospitalier de l'Université Laval","funders":"Ministry of Education, Culture, Sports, Science and Technology","keywords":"Neurofilament; Phosphorylation; Biology; Mutant; Cell biology; Kinase; In vitro; Protein filament; Intermediate filament; Mutation; Oligomer; Cyclin-dependent kinase 5; Molecular biology; Protein kinase A; Cytoskeleton; Biochemistry; Gene; Cyclin-dependent kinase 2; Chemistry; Cell; Immunology","score_opus":0.020192556822836532,"score_gpt":0.241704009265546,"score_spread":0.22151145244270948,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1995784041","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":[0.99856156,0.00027950274,0.00054539385,0.000019598663,0.00000789718,0.0000074916743,0.00020507387,0.000020894886,0.0003527253],"genre_scores_gemma":[0.99736553,0.0002495896,0.00079887523,0.00001804438,0.0000043604355,0.000025702477,0.00043317667,0.000018599567,0.0010861278],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9998889,0.00001812481,0.000016314141,0.000027612168,0.000028965467,0.00002008121],"domain_scores_gemma":[0.9998795,0.000017319808,0.000046586058,0.000011490975,0.000009215427,0.00003595469],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00010403372,0.00043905957,0.00020753256,0.0002231609,0.00017947303,0.00021754568,0.00013899962,0.0002755031,0.0006063712],"category_scores_gemma":[0.000114961214,0.00017353668,0.00023729862,0.00012429681,0.00015099627,0.00012433404,0.00016479276,0.00034364153,0.00021523735],"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":[0.00006640959,0.000018040631,0.00017820991,0.0000124577555,0.0000054465236,0.000083633626,0.0000167228,0.000059591595,0.9992926,0.000033634657,0.000016080474,0.00021719783],"study_design_scores_gemma":[0.000017117834,0.00023698734,0.010454981,0.000005635127,0.000016501355,0.00057212973,0.000030376963,0.0014499634,0.9864248,0.00005564929,0.0007293277,0.000006543361],"about_ca_topic_score_codex":0.0008282473,"about_ca_topic_score_gemma":0.000893166,"teacher_disagreement_score":0.0008282473,"about_ca_system_score_codex":0.0003069888,"about_ca_system_score_gemma":0.00008824694,"threshold_uncertainty_score":0.0022274256},"labels":[],"label_agreement":null},{"id":"W1997932611","doi":"10.1097/00003086-200104000-00036","title":"Hereditary Neuropathy With Liability to Pressure Palsies","year":2001,"lang":"en","type":"article","venue":"Clinical Orthopaedics and Related Research","topic":"Hereditary Neurological Disorders","field":"Neuroscience","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":"Cegep de Sept Iles","funders":"","keywords":"Medicine; Weakness; Peripheral neuropathy; Palsy; Pediatrics; Surgery; Pathology; Endocrinology","score_opus":0.14521028566539892,"score_gpt":0.41775769484661046,"score_spread":0.27254740918121156,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1997932611","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":[0.940678,0.007868811,0.005673227,0.0012831578,0.00024232222,0.000120707686,0.00038768415,0.0005641465,0.0431819],"genre_scores_gemma":[0.9895515,0.0024340604,0.0009593232,0.00027431155,0.00018783129,0.000017418908,0.00015535168,0.000029722712,0.006390532],"study_design_codex":"case_report","study_design_gemma":"case_report","domain_scores_codex":[0.9997023,0.000038580634,0.000023069384,0.00006241959,0.000086774315,0.00008682456],"domain_scores_gemma":[0.99957997,0.00012753546,0.0001247076,0.000030214487,0.00004301284,0.00009451259],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00017928968,0.000965203,0.00051947194,0.00082504126,0.0009530309,0.00040826376,0.00035764577,0.0006988245,0.0062493854],"category_scores_gemma":[0.0017839873,0.0001769637,0.00020190811,0.0007756519,0.0006736016,0.00040710773,0.00075367704,0.0004999311,0.00079489284],"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":[0.00013953794,0.000089096626,0.028990015,0.0002081079,0.000037322687,0.92678547,0.00068042043,0.00023726992,0.009444513,0.0022802353,0.0035271097,0.027580766],"study_design_scores_gemma":[0.000012131042,0.00014287587,0.021028752,0.00005343379,0.000032396376,0.97083867,0.00014880774,0.00019886695,0.0019667104,0.0008333165,0.004733689,0.000010384863],"about_ca_topic_score_codex":0.0011777988,"about_ca_topic_score_gemma":0.001471638,"teacher_disagreement_score":0.0062493854,"about_ca_system_score_codex":0.0002731919,"about_ca_system_score_gemma":0.00034012264,"threshold_uncertainty_score":0.02090633},"labels":[],"label_agreement":null},{"id":"W1999695324","doi":"10.1007/s00415-006-0505-4","title":"The role of hereditary spastic paraplegia related genes in multiple sclerosis","year":2007,"lang":"en","type":"article","venue":"Journal of Neurology","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":16,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of British Columbia","funders":"","keywords":"Multiple sclerosis; Hereditary spastic paraplegia; Disease; Neurology; Gene; Medicine; Pathogenesis; Biology; Genetics; Neuroscience; Pathology; Phenotype; Immunology","score_opus":0.042467427299351344,"score_gpt":0.24379366820136852,"score_spread":0.20132624090201717,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1999695324","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":[0.96283484,0.029431427,0.00071383413,0.0014567098,0.00007927512,0.0000062349777,0.000094829156,0.000021915539,0.0053609707],"genre_scores_gemma":[0.99319816,0.0046492023,0.0005491419,0.00015479371,0.00011197121,0.000005055322,0.00006137032,0.0000049379323,0.0012654605],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.999913,0.00003794202,0.0000076454035,0.0000129018,0.000013996746,0.000014581475],"domain_scores_gemma":[0.999683,0.00017777868,0.000051652885,0.000016002386,0.000027905968,0.00004371537],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00030161167,0.00033842985,0.00026263067,0.0006940385,0.00034787934,0.000369216,0.00029017165,0.00051628705,0.0011852437],"category_scores_gemma":[0.0005247739,0.000118547854,0.000148129,0.00028326613,0.0005722168,0.00033494277,0.00023589165,0.00027118615,0.00012985105],"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":[0.011413521,0.00070457667,0.275941,0.0011019321,0.00094098045,0.06619952,0.0014004658,0.0072075133,0.39285865,0.03519673,0.008080199,0.19895484],"study_design_scores_gemma":[0.0007778178,0.002393638,0.77602196,0.0004943833,0.0014014782,0.07371897,0.0016528156,0.009514545,0.060321216,0.037781496,0.035829507,0.00009215698],"about_ca_topic_score_codex":0.0010512098,"about_ca_topic_score_gemma":0.0011292057,"teacher_disagreement_score":0.0011852437,"about_ca_system_score_codex":0.00023877084,"about_ca_system_score_gemma":0.00027735505,"threshold_uncertainty_score":0.00396502},"labels":[],"label_agreement":null},{"id":"W1999848546","doi":"10.1097/wco.0b013e32833c7a19","title":"Sensory neuropathies, from symptoms to treatment","year":2010,"lang":"en","type":"review","venue":"Current Opinion in Neurology","topic":"Hereditary Neurological Disorders","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","funders":"","keywords":"Medicine; Sensory system; Disease; Sensory neuropathy; Dermatology; Pathology; Surgery; Neuroscience; Psychology","score_opus":0.18734146647008007,"score_gpt":0.3997541954987876,"score_spread":0.21241272902870753,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1999848546","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":[0.00014005664,0.9973381,0.00007705404,0.00039556157,0.00039574964,0.000005100643,0.000017106951,0.0000071963877,0.0016239589],"genre_scores_gemma":[0.0011119636,0.9966743,0.000104017934,0.00040521566,0.00055682124,0.000006753897,0.000033285276,0.0000020810899,0.001105569],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.9998324,0.000027613925,0.000029682882,0.00003431978,0.000056771627,0.000019291843],"domain_scores_gemma":[0.99981016,0.00007298794,0.000040063114,0.000005904836,0.00005055168,0.00002037768],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00033637846,0.000999775,0.001717651,0.0017724608,0.00027214087,0.001012463,0.00083280646,0.000998333,0.0056207934],"category_scores_gemma":[0.0007352764,0.00020262052,0.000361073,0.0014073096,0.000560962,0.0011621686,0.0005774127,0.0011997757,0.003988448],"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":[0.00009387878,0.0000616921,0.00028367867,0.015764624,0.00007570224,0.0010223195,0.000051303898,0.0002533178,0.0009430748,0.0015277433,0.055524338,0.92439824],"study_design_scores_gemma":[0.00006231958,0.00014619002,0.00322206,0.019805076,0.00020746309,0.019168792,0.00021463372,0.00014761466,0.0007090851,0.003844649,0.952437,0.000035233606],"about_ca_topic_score_codex":0.0013062496,"about_ca_topic_score_gemma":0.0023534568,"teacher_disagreement_score":0.0056207934,"about_ca_system_score_codex":0.00063297484,"about_ca_system_score_gemma":0.0009735267,"threshold_uncertainty_score":0.018803477},"labels":[],"label_agreement":null},{"id":"W1999933973","doi":"10.1111/j.1399-0004.2010.01591.x","title":"Recent advances in the genetics of distal hereditary motor neuropathy give insight to a disease mechanism involving copper homeostasis that may extend to other motor neuron disorders","year":2010,"lang":"en","type":"article","venue":"Clinical Genetics","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":7,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Centre Hospitalier de l’Université de Montréal; Université de Montréal","funders":"","keywords":"Neuroscience; Motor neuron; Mechanism (biology); Disease; Menkes disease; Biology; ATP7A; Genetics; Medicine; Gene; Pathology; Copper metabolism; Chemistry; Copper; Transporter; Spinal cord; Physics","score_opus":0.059048513000987055,"score_gpt":0.3311006524794773,"score_spread":0.2720521394784902,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W1999933973","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":[0.2527928,0.57520217,0.06452849,0.061063748,0.0020330301,0.00014052732,0.0005093615,0.00081886083,0.042910993],"genre_scores_gemma":[0.524016,0.4229263,0.036466707,0.0040649595,0.0028623904,0.00006237025,0.00044156602,0.00005667903,0.009103002],"study_design_codex":"design_other","study_design_gemma":"observational","domain_scores_codex":[0.99977034,0.000068969704,0.00003125265,0.000048536796,0.000058371992,0.0000225489],"domain_scores_gemma":[0.99942267,0.00022042858,0.00016317233,0.000027216793,0.000073692085,0.00009272017],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0004920665,0.0005988545,0.00043258388,0.0008836216,0.00016478333,0.0003607673,0.00036582063,0.0009647608,0.0023185695],"category_scores_gemma":[0.00072190526,0.00014671304,0.00024905626,0.00056889333,0.0009043114,0.00070399727,0.0004858004,0.0009168333,0.00055679824],"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":[0.00071346265,0.00023115141,0.042533364,0.0019827196,0.00022213573,0.038101953,0.0003559577,0.0019797743,0.106539875,0.020889878,0.016510813,0.76993895],"study_design_scores_gemma":[0.00024341328,0.0012454389,0.19338395,0.0008248154,0.00095129444,0.2759296,0.0010266566,0.0040557627,0.04778439,0.082127094,0.39217165,0.00025600358],"about_ca_topic_score_codex":0.00068054366,"about_ca_topic_score_gemma":0.0015394299,"teacher_disagreement_score":0.0023185695,"about_ca_system_score_codex":0.00038107389,"about_ca_system_score_gemma":0.0003759194,"threshold_uncertainty_score":0.0077563524},"labels":[],"label_agreement":null},{"id":"W2000038554","doi":"10.1111/j.1529-8027.2012.00405.x","title":"Two novel missense mutations in <i>FGD4/FRABIN</i> cause Charcot‐Marie‐Tooth type 4H (CMT4H)","year":2012,"lang":"en","type":"article","venue":"Journal of the Peripheral Nervous System","topic":"Hereditary Neurological Disorders","field":"Neuroscience","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":"Agence Universitaire de la Francophonie","keywords":"Missense mutation; Tooth disease; Genetics; Medicine; Mutation; Coding region; Biology; Gene","score_opus":0.04771040696254374,"score_gpt":0.27996286229056666,"score_spread":0.2322524553280229,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2000038554","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":[0.99884206,0.00016157437,0.00030896632,0.000034925353,0.000009851598,0.000020596743,0.00017205982,0.000013665646,0.0004363051],"genre_scores_gemma":[0.998781,0.00006548884,0.00049846614,0.000053577052,0.00001703441,0.000015536536,0.00021668391,0.000007404983,0.0003447886],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9997131,0.00002283797,0.000035627374,0.00008069921,0.0000650288,0.000082662984],"domain_scores_gemma":[0.9995666,0.00014122222,0.00014325777,0.0000224407,0.000032427717,0.000094098694],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00018415417,0.0010934772,0.00050662964,0.00094742223,0.0007323376,0.00041805799,0.0005474096,0.0010088177,0.0022236872],"category_scores_gemma":[0.0010471646,0.0003027326,0.00043947747,0.0005480139,0.00074032956,0.00019385645,0.00048673488,0.0003857281,0.00033159967],"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":[0.0010672202,0.00039562274,0.4741343,0.00020845975,0.00035288028,0.37696987,0.0028861717,0.0006217473,0.115860246,0.0005506632,0.0011890355,0.0257637],"study_design_scores_gemma":[0.00021476983,0.0006224227,0.52920926,0.00004552259,0.0002541585,0.44163418,0.00068438065,0.00075805094,0.022116888,0.00034622793,0.0040245466,0.000089568755],"about_ca_topic_score_codex":0.0027623866,"about_ca_topic_score_gemma":0.0024214343,"teacher_disagreement_score":0.0027623866,"about_ca_system_score_codex":0.00044502196,"about_ca_system_score_gemma":0.00028879225,"threshold_uncertainty_score":0.0074390173},"labels":[],"label_agreement":null},{"id":"W2000430768","doi":"10.1002/mus.20078","title":"Resistance training exercise and creatine in patients with Charcot–Marie–Tooth disease","year":2004,"lang":"en","type":"article","venue":"Muscle & Nerve","topic":"Hereditary Neurological Disorders","field":"Neuroscience","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":"McMaster University Medical Centre","funders":"","keywords":"Creatine; Creatine Monohydrate; Resistance training; Placebo; Medicine; Internal medicine; Strength training; Physical therapy; Physical medicine and rehabilitation; Endocrinology; Pathology","score_opus":0.021172080246021883,"score_gpt":0.21559248884333876,"score_spread":0.19442040859731688,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2000430768","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":[0.99797064,0.0016191424,0.00002800542,0.000057163972,0.000006866473,0.0000065946624,0.000014895881,0.0000063224593,0.00029028128],"genre_scores_gemma":[0.999113,0.00047728277,0.000112811766,0.00008623197,0.000018077788,0.000010145595,0.000051726132,0.0000012232388,0.0001294463],"study_design_codex":"observational","study_design_gemma":"nonrandomized_trial","domain_scores_codex":[0.99978524,0.00008812442,0.00002721597,0.00003699956,0.00003459108,0.000027944827],"domain_scores_gemma":[0.99973375,0.00008033904,0.00009042432,0.000007666476,0.000016605625,0.00007123641],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00032218453,0.00043214142,0.0008846961,0.00024056465,0.0003731076,0.0002535286,0.00014673697,0.0005798341,0.0006086053],"category_scores_gemma":[0.00088333373,0.0001693392,0.00029170973,0.00024564148,0.00022149134,0.00016666773,0.00013342153,0.00029645895,0.00011524988],"study_design_candidate":"nonrandomized_trial","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":[0.045007564,0.0041738926,0.80849713,0.00067715376,0.0011128661,0.006969846,0.00066072296,0.00067582383,0.050823566,0.00007792595,0.00088740664,0.08043613],"study_design_scores_gemma":[0.0012601522,0.013560749,0.9781807,0.000041803298,0.00040383887,0.0039001093,0.00017835452,0.0003915148,0.0013636615,0.00005542454,0.0006494885,0.0000141584105],"about_ca_topic_score_codex":0.001167925,"about_ca_topic_score_gemma":0.0027340373,"teacher_disagreement_score":0.001167925,"about_ca_system_score_codex":0.0002436978,"about_ca_system_score_gemma":0.00014199885,"threshold_uncertainty_score":0.0023223162},"labels":[],"label_agreement":null},{"id":"W2001594359","doi":"10.2340/16501977-0932","title":"A thumb opposition splint to improve manual dexterity and upper-limb functioning in Charcot-Marie-Tooth disease","year":2012,"lang":"en","type":"article","venue":"Journal of Rehabilitation Medicine","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":29,"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; Physical therapy; Thumb; Activities of daily living; Tolerability; Upper limb; Physical medicine and rehabilitation; Outpatient clinic; Surgery","score_opus":0.019761040703132764,"score_gpt":0.30059995715054216,"score_spread":0.2808389164474094,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2001594359","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":[0.99928635,0.00032512084,0.000131839,0.000016765076,0.000004643238,0.000033889355,0.000009287703,0.0000066657744,0.0001855356],"genre_scores_gemma":[0.9986343,0.00025780484,0.00067769154,0.00003791852,0.00001258296,0.000059963175,0.000034565066,0.0000013515397,0.0002837574],"study_design_codex":"design_other","study_design_gemma":"observational","domain_scores_codex":[0.9998691,0.000044190416,0.000014233238,0.000019490557,0.000033343666,0.000019618748],"domain_scores_gemma":[0.99982136,0.000059156147,0.000050785788,0.0000090364865,0.000014884262,0.000044818767],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00037862995,0.00033030353,0.00036718012,0.00012863394,0.0001841331,0.00011403416,0.00014178212,0.00020168127,0.0010637561],"category_scores_gemma":[0.0006384319,0.00007180211,0.00018758856,0.00008961206,0.00018093818,0.000104087994,0.000120804936,0.00022864877,0.00010845131],"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":[0.05177127,0.028542439,0.11879594,0.0012265096,0.00038855267,0.002603481,0.00070732256,0.0012581311,0.21012914,0.00009039476,0.0010407792,0.58344615],"study_design_scores_gemma":[0.005787318,0.3273268,0.63271123,0.00011911958,0.0003113615,0.006796991,0.0003627951,0.0014204463,0.023577875,0.000081434555,0.0014779555,0.000026697171],"about_ca_topic_score_codex":0.00030065046,"about_ca_topic_score_gemma":0.0007332028,"teacher_disagreement_score":0.0010637561,"about_ca_system_score_codex":0.00013511175,"about_ca_system_score_gemma":0.00019128041,"threshold_uncertainty_score":0.0035586357},"labels":[],"label_agreement":null},{"id":"W2009724266","doi":"10.1002/ana.21114","title":"Characterization of a novel SPG3A deletion in a French‐Canadian family","year":2007,"lang":"en","type":"article","venue":"Annals of Neurology","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":22,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":true,"ca_institutions":"Centre Hospitalier Universitaire de Sherbrooke; Université Laval; McGill University; Centre Hospitalier de l’Université de Montréal; Centre hospitalier universitaire de Québec; Université de Sherbrooke; Hôpital Notre-Dame","funders":"Canadian Institutes of Health Research; National Institutes of Health","keywords":"Hereditary spastic paraplegia; Genetics; Triphosphatase; Spasticity; Gene; Biology; Mutation; Phenotype; Guanosine; Medicine; Physical medicine and rehabilitation","score_opus":0.10696750172646342,"score_gpt":0.3081889952399594,"score_spread":0.201221493513496,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2009724266","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":[0.98827493,0.00062077085,0.0015068211,0.001055086,0.00008366113,0.00008027838,0.0011866498,0.00008502301,0.0071067014],"genre_scores_gemma":[0.99205303,0.0005117857,0.0017084497,0.0004134969,0.000051824303,0.000029344888,0.0005122989,0.0000362333,0.0046835546],"study_design_codex":"case_report","study_design_gemma":"observational","domain_scores_codex":[0.9996649,0.000021348165,0.000016964397,0.000100071105,0.0001288803,0.000067935616],"domain_scores_gemma":[0.99959475,0.00009265515,0.00003821701,0.000013316225,0.000108466054,0.00015262215],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00020365404,0.001988659,0.000530041,0.0018704819,0.0033491212,0.0005501665,0.0008573372,0.0013397977,0.004911687],"category_scores_gemma":[0.00096664793,0.00039274315,0.00058492913,0.0012236632,0.0012287531,0.00021956324,0.00066465157,0.0007599856,0.0004757001],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":true,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00061217207,0.0003383461,0.09404825,0.00019814004,0.00019886547,0.716966,0.0077265487,0.0011543444,0.12662894,0.003956106,0.0061441893,0.042028196],"study_design_scores_gemma":[0.00013042122,0.00041261702,0.27924752,0.00012116199,0.00021988535,0.68136615,0.0020101757,0.0018426953,0.010719356,0.0006466486,0.023128709,0.00015468594],"about_ca_topic_score_codex":0.43966815,"about_ca_topic_score_gemma":0.43019587,"teacher_disagreement_score":0.5603318,"about_ca_system_score_codex":0.002522967,"about_ca_system_score_gemma":0.0042212787,"threshold_uncertainty_score":0.874218},"labels":[],"label_agreement":null},{"id":"W2011314424","doi":"10.1371/journal.pgen.1001081","title":"Mutation in the Gene Encoding Ubiquitin Ligase LRSAM1 in Patients with Charcot-Marie-Tooth Disease","year":2010,"lang":"en","type":"article","venue":"PLoS Genetics","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":71,"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; Izaak Walton Killam Health Centre; Dalhousie University","funders":"Genome Atlantic; IWK Health Centre; Dalhousie University; Nova Scotia Health Research Foundation; Genome Canada; Dalhousie Medical Research Foundation","keywords":"Biology; Genetics; Exon; Frameshift mutation; Gene; Parkin; Exon skipping; Molecular biology; Alternative splicing; Disease; Parkinson's disease","score_opus":0.0226431642549139,"score_gpt":0.22791069068708492,"score_spread":0.20526752643217103,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2011314424","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":[0.99807584,0.0003480108,0.00029372305,0.000158753,0.0000135622395,0.00002358213,0.00020420577,0.00004478876,0.0008375331],"genre_scores_gemma":[0.9989053,0.00014296298,0.00032527812,0.000059662478,0.000013909823,0.00000548194,0.000106456486,0.000005952423,0.00043489554],"study_design_codex":"case_report","study_design_gemma":"observational","domain_scores_codex":[0.9997423,0.000018701086,0.000024514433,0.000090969326,0.000067698915,0.00005580138],"domain_scores_gemma":[0.9997727,0.00005621833,0.00005317566,0.000011374217,0.0000307183,0.00007576396],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00019439824,0.0014887424,0.0005633904,0.0011638829,0.0018353908,0.0005458447,0.00062714383,0.0012719743,0.0018597374],"category_scores_gemma":[0.0009112639,0.00032297615,0.00027663988,0.0011197628,0.0008856175,0.00021845545,0.00045618782,0.0005205696,0.00028890267],"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":[0.0015573165,0.00042274097,0.39546117,0.00025358665,0.00028144752,0.44610536,0.0043170024,0.0011674289,0.113204576,0.00077879534,0.0026461103,0.0338044],"study_design_scores_gemma":[0.00012517194,0.0005981097,0.629804,0.00007881315,0.00036070563,0.35189128,0.0010646657,0.0020426987,0.009774773,0.0004680718,0.0037110092,0.000080674],"about_ca_topic_score_codex":0.033739727,"about_ca_topic_score_gemma":0.03898814,"teacher_disagreement_score":0.033739727,"about_ca_system_score_codex":0.0011406721,"about_ca_system_score_gemma":0.000969309,"threshold_uncertainty_score":0.06708664},"labels":[],"label_agreement":null},{"id":"W2013104342","doi":"10.1017/s0317167100006892","title":"Two Causes of Demyelinating Neuropathy in One Patient: CMT1A and POEMS Syndrome","year":2007,"lang":"en","type":"letter","venue":"Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":8,"is_retracted":false,"has_abstract":true,"route_ca_aff":false,"route_ca_fund":false,"route_ca_venue":true,"route_about_ca":false,"ca_institutions":"","funders":"National Institute of Neurological Disorders and Stroke; National Institutes of Health","keywords":"POEMS syndrome; Action (physics); Medicine; Content (measure theory); Surgery; Polyneuropathy; Mathematics; Physics","score_opus":0.06656601683070872,"score_gpt":0.27659420410048324,"score_spread":0.2100281872697745,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2013104342","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":[0.9681654,0.0017888994,0.0016480311,0.009357011,0.0008977891,0.0002127991,0.00036150322,0.00016504768,0.01740354],"genre_scores_gemma":[0.99146503,0.00072401896,0.0012992952,0.002029936,0.0014980463,0.00006430588,0.00015203858,0.00004403784,0.0027234335],"study_design_codex":"case_report","study_design_gemma":"case_report","domain_scores_codex":[0.9987074,0.00021973331,0.00015946515,0.00035565766,0.0001757345,0.00038204048],"domain_scores_gemma":[0.9963921,0.001791607,0.00042025847,0.00023267083,0.0002201348,0.00094329694],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.000716972,0.0023950315,0.00176181,0.0024731266,0.003096775,0.0019169791,0.0016095266,0.010808477,0.005880439],"category_scores_gemma":[0.00971164,0.0013866752,0.0012333414,0.0017607119,0.0020275821,0.0024134777,0.0016912741,0.0048240344,0.0015231436],"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":[0.00010023786,0.00006447559,0.006382326,0.000028976325,0.000010834613,0.990595,0.00025593437,0.00007275871,0.00037556756,0.00030123096,0.0005478319,0.0012647392],"study_design_scores_gemma":[0.00008535327,0.00011934315,0.006909009,0.000018045328,0.0000141081,0.99139774,0.00014245021,0.00021078491,0.00020112451,0.00040879459,0.00047280357,0.000020417245],"about_ca_topic_score_codex":0.002831948,"about_ca_topic_score_gemma":0.002379793,"teacher_disagreement_score":0.010808477,"about_ca_system_score_codex":0.0018525539,"about_ca_system_score_gemma":0.0011082725,"threshold_uncertainty_score":0.019672036},"labels":[],"label_agreement":null},{"id":"W2013340140","doi":"10.1007/s12017-013-8271-9","title":"The Role of Reticulons in Neurodegenerative Diseases","year":2013,"lang":"en","type":"review","venue":"NeuroMolecular Medicine","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":76,"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":"Cambridge Institute for Medical Research, University of Cambridge; Ministero della Salute; Canada Excellence Research Chairs, Government of Canada","keywords":"Neurodegeneration; Biology; Neuroscience; Cell biology; Pyrin domain; Endoplasmic reticulum; Disease; Pathology; Medicine; Genetics; Receptor; Inflammasome","score_opus":0.04776754247483672,"score_gpt":0.3173972102668848,"score_spread":0.26962966779204806,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2013340140","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":[0.00012021195,0.99860734,0.00009593908,0.00014859975,0.00009981424,0.000002588972,0.0000073480687,0.000006297899,0.0009118303],"genre_scores_gemma":[0.00091613486,0.99807173,0.00018049177,0.00009684339,0.00013918053,0.000004365508,0.000018439308,0.0000011346112,0.0005716963],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.9998865,0.000018622197,0.000019923467,0.000020624731,0.00004278233,0.000011509383],"domain_scores_gemma":[0.99986064,0.000047958732,0.000022269132,0.00000489523,0.000044209384,0.000020011326],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00036632144,0.00072954124,0.0009548095,0.0021957804,0.00031882676,0.0006699239,0.0005747703,0.0008054981,0.0027454358],"category_scores_gemma":[0.00039012101,0.00019393004,0.0002908078,0.0018772894,0.00044893482,0.0009954817,0.0006723352,0.0011448751,0.0020383145],"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":[0.00006402686,0.000056215573,0.00021644066,0.0093944045,0.00006818744,0.00039327485,0.000077059274,0.00024551217,0.0027550429,0.003435203,0.021407478,0.9618871],"study_design_scores_gemma":[0.00001591105,0.00007033224,0.0010688852,0.0017078597,0.0000755063,0.0029541804,0.000055618973,0.00007359756,0.00067475304,0.002104992,0.9911828,0.000015577163],"about_ca_topic_score_codex":0.0009549409,"about_ca_topic_score_gemma":0.0016295051,"teacher_disagreement_score":0.0027454358,"about_ca_system_score_codex":0.0005372213,"about_ca_system_score_gemma":0.00087456894,"threshold_uncertainty_score":0.00918442},"labels":[],"label_agreement":null},{"id":"W2017371768","doi":"10.1016/j.nbd.2010.01.001","title":"Lack of evidence for a pathogenic role of T-lymphocytes in an animal model for Charcot-Marie-Tooth disease 1A","year":2010,"lang":"en","type":"article","venue":"Neurobiology of Disease","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":16,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"McGill University Health Centre","funders":"Deutsche Forschungsgemeinschaft","keywords":"Myelin; Pathological; Mutant; Biology; Immune system; Immunology; Disease; Lymphocyte; T lymphocyte; Neuroscience; Pathology; Medicine; Genetics; Central nervous system; Gene","score_opus":0.16803966428983214,"score_gpt":0.3606249695270896,"score_spread":0.19258530523725748,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2017371768","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":[0.97265404,0.006073263,0.00591822,0.0011631221,0.00032520827,0.00010583916,0.0012266638,0.0003954379,0.012138131],"genre_scores_gemma":[0.98564804,0.0037089214,0.003314345,0.00041195325,0.00014201859,0.0001926357,0.0013781661,0.000105833155,0.005097973],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9990828,0.00018856871,0.000113703856,0.00021188291,0.00028522295,0.00011780426],"domain_scores_gemma":[0.99733907,0.0012030152,0.00034030306,0.00036758816,0.00031017736,0.00043983845],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.001512607,0.00077770016,0.0006719672,0.003112174,0.0005723968,0.00078404223,0.0014691841,0.0022233075,0.007885416],"category_scores_gemma":[0.0017410384,0.0002938277,0.0006035578,0.00047930365,0.0011532573,0.0009967871,0.00051900325,0.0010708068,0.00142892],"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":[0.0027962732,0.0011282734,0.0045802146,0.00085181295,0.00022620863,0.004615946,0.00019545069,0.0002798629,0.97117054,0.0024267037,0.0011395979,0.01058906],"study_design_scores_gemma":[0.0007262968,0.0056239194,0.033503607,0.00045144142,0.0012621712,0.032540455,0.00084539107,0.0032958216,0.8872117,0.006687661,0.027759295,0.00009223156],"about_ca_topic_score_codex":0.0005794695,"about_ca_topic_score_gemma":0.0005631099,"teacher_disagreement_score":0.007885416,"about_ca_system_score_codex":0.00036357238,"about_ca_system_score_gemma":0.00045754897,"threshold_uncertainty_score":0.026379406},"labels":[],"label_agreement":null},{"id":"W2020167372","doi":"10.1371/journal.pone.0006975","title":"Crystal Structure of the ATPase Domain of the Human AAA+ Protein Paraplegin/SPG7","year":2009,"lang":"en","type":"article","venue":"PLoS ONE","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":38,"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; Knut och Alice Wallenbergs Stiftelse; Karolinska Institutet; Stiftelsen för Strategisk Forskning; University of Oxford; Ontario Genomics Institute; Ontario Genomics; Genome Canada; GlaxoSmithKline; Ontario Innovation Trust; European Synchrotron Radiation Facility; Wellcome Trust","keywords":"AAA proteins; Random hexamer; Computational biology; Protein domain; Biology; Protease; Protein structure; Homology modeling; Chemistry; ATPase; Cell biology; Biochemistry; Enzyme; Gene","score_opus":0.04069736476153729,"score_gpt":0.22989213345515522,"score_spread":0.18919476869361793,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2020167372","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":[0.9293163,0.012029278,0.0073596016,0.002481479,0.0007281591,0.00011789992,0.017228713,0.0020510124,0.028687596],"genre_scores_gemma":[0.8913282,0.0061187623,0.026345335,0.00060905464,0.00011031201,0.00019758331,0.057913188,0.0007806564,0.016596941],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99987066,0.000008972234,0.0000037226048,0.000017000739,0.00008059955,0.000019073183],"domain_scores_gemma":[0.999907,0.000028133338,0.000010388242,0.000003091775,0.000028814236,0.000022557942],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00016039556,0.00045925032,0.0005648397,0.00021214329,0.0005031351,0.0005107993,0.0007283401,0.0007043161,0.009934665],"category_scores_gemma":[0.0002410576,0.00022388207,0.00021040245,0.0004621897,0.0001364876,0.00026775658,0.00030579962,0.0009901645,0.0019596647],"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":[0.0024821602,0.0012967425,0.010710346,0.003315494,0.0004832354,0.004949371,0.0013505224,0.014681532,0.6372786,0.008689834,0.20279188,0.111970276],"study_design_scores_gemma":[0.0030705791,0.001097559,0.08711307,0.00082236575,0.00075269776,0.005538991,0.0020449727,0.16653179,0.3026368,0.0062003303,0.4239055,0.0002853719],"about_ca_topic_score_codex":0.0033738536,"about_ca_topic_score_gemma":0.004893886,"teacher_disagreement_score":0.009934665,"about_ca_system_score_codex":0.0005782452,"about_ca_system_score_gemma":0.0005592491,"threshold_uncertainty_score":0.033234775},"labels":[],"label_agreement":null},{"id":"W2022508337","doi":"10.5301/hipint.5000061","title":"Early Results of the Bernese Periacetabular Osteotomy for Symptomatic Dysplasia in Charcot-Marie-Tooth Disease","year":2013,"lang":"en","type":"article","venue":"Hip International","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":11,"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; WOMAC; Heterotopic ossification; Hip dysplasia; Radiography; Osteoarthritis; Surgery; Concomitant; Dysplasia; Femoral head; Harris Hip Score; Osteotomy; Retrospective cohort study; Internal medicine","score_opus":0.02003607181861074,"score_gpt":0.2510436340739563,"score_spread":0.23100756225534555,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2022508337","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":[0.99847907,0.000822468,0.00012728365,0.000026468513,0.000005607888,0.000010006135,0.00004206542,0.0000057756747,0.00048127692],"genre_scores_gemma":[0.99952173,0.00014833055,0.00010056666,0.000013525402,0.0000074077398,0.0000034102015,0.00006329398,0.0000014603228,0.00014040868],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.999642,0.00006143316,0.000046955774,0.00003080842,0.0001430002,0.00007574763],"domain_scores_gemma":[0.9989127,0.0002537654,0.00042244472,0.000045139306,0.00013381708,0.00023210619],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00038276962,0.00039294464,0.00031358298,0.00083603855,0.00039991853,0.0003001521,0.00024721448,0.00029723553,0.0010110221],"category_scores_gemma":[0.0018126563,0.00015889312,0.0003434573,0.0002881668,0.0003453268,0.00020811812,0.00035122473,0.00026482096,0.00017191135],"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":[0.0011154722,0.00021006777,0.93595886,0.00013866993,0.000110203604,0.019204676,0.00030301992,0.00024174986,0.008794322,0.000028705972,0.00024958848,0.033644617],"study_design_scores_gemma":[0.000017675755,0.0008352598,0.95458615,0.00002504562,0.00003526072,0.04284418,0.00014783238,0.00012253421,0.001077877,0.000017094915,0.00028213108,0.0000090369895],"about_ca_topic_score_codex":0.0017287122,"about_ca_topic_score_gemma":0.0051753605,"teacher_disagreement_score":0.0017287122,"about_ca_system_score_codex":0.00047034194,"about_ca_system_score_gemma":0.00035709675,"threshold_uncertainty_score":0.0034372807},"labels":[],"label_agreement":null},{"id":"W2022645386","doi":"10.1006/nbdi.2000.0323","title":"PMP22 Carrying the Trembler or Trembler-J Mutation Is Intracellularly Retained in Myelinating Schwann Cells","year":2000,"lang":"en","type":"article","venue":"Neurobiology of Disease","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":95,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"McGill University","funders":"","keywords":"Endoplasmic reticulum; Biology; Myelin; Mutant; Cell biology; Molecular biology; Epitope; Cytoplasm; Peripheral myelin protein 22; Gene; Phenotype; Genetics; Neuroscience; Central nervous system; Antigen","score_opus":0.03399166585262556,"score_gpt":0.2619496527639774,"score_spread":0.22795798691135186,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2022645386","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":[0.99850637,0.0002523816,0.00043128946,0.000027089498,0.00001592482,0.0000024672404,0.00006037383,0.00003108087,0.0006729278],"genre_scores_gemma":[0.9983815,0.00013251527,0.00026457664,0.000017688497,0.000009502353,0.000006287624,0.00019056376,0.000014846606,0.0009824937],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9998944,0.000014626788,0.000009720756,0.000023297964,0.000030471849,0.00002743865],"domain_scores_gemma":[0.9998134,0.00002178558,0.000059744234,0.000019343188,0.000022333923,0.00006351315],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.000080012054,0.00034646675,0.00026369098,0.0003110823,0.00027157582,0.00037385637,0.00020786824,0.00044155293,0.0015580731],"category_scores_gemma":[0.00024973514,0.00015258636,0.00014298379,0.00017566615,0.00028440784,0.00022257864,0.00029977233,0.0003296514,0.0008494229],"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":[0.00015243112,0.000018231674,0.001238095,0.000022743672,0.000010996107,0.002891455,0.000036068675,0.000039509974,0.9945102,0.00011087801,0.000054871012,0.00091444235],"study_design_scores_gemma":[0.00010259779,0.00075816805,0.07673049,0.00002606497,0.00009546134,0.06498027,0.00039533738,0.0014912658,0.84853214,0.00045649862,0.006386029,0.00004567483],"about_ca_topic_score_codex":0.00054960436,"about_ca_topic_score_gemma":0.0004424268,"teacher_disagreement_score":0.0015580731,"about_ca_system_score_codex":0.00016484917,"about_ca_system_score_gemma":0.00010461279,"threshold_uncertainty_score":0.0052122474},"labels":[],"label_agreement":null},{"id":"W2024555394","doi":"10.1002/humu.22032","title":"An analysis of exome sequencing for diagnostic testing of the genes associated with muscle disease and spastic paraplegia","year":2012,"lang":"en","type":"article","venue":"Human Mutation","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":34,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of British Columbia; Child and Family Research Institute; Children's & Women's Health Centre of British Columbia","funders":"National Human Genome Research Institute; Canadian Child Health Clinician Scientist Program; Rare Disease Foundation; National Institutes of Health; Child and Family Research Institute","keywords":"Biology; Exome sequencing; Hereditary spastic paraplegia; Paraplegia; Genetics; Gene; Disease; Muscle disease; Exome; Computational biology; Neuromuscular disease; Spastic; Bioinformatics; Pathology; Phenotype; Neuroscience; Physical medicine and rehabilitation; Spinal cord; Medicine","score_opus":0.08450201189719213,"score_gpt":0.29517732599220525,"score_spread":0.2106753140950131,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2024555394","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":[0.9846333,0.00094459765,0.011450055,0.00011965346,0.000012204269,0.0000948646,0.0007446207,0.0000650015,0.0019356273],"genre_scores_gemma":[0.9857243,0.00047677298,0.0121145705,0.0001469823,0.000009845839,0.0000624931,0.0008403017,0.00001624054,0.00060852326],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.998814,0.0005210919,0.00007242041,0.0001979659,0.00033271575,0.00006194517],"domain_scores_gemma":[0.99774086,0.0015649013,0.00025402624,0.00012407577,0.0002515317,0.0000645669],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0019078319,0.0003857621,0.00023395038,0.0012513876,0.00022770738,0.00040821216,0.00016926027,0.00039153924,0.0010786323],"category_scores_gemma":[0.003588801,0.000093914736,0.00022880273,0.0004430683,0.00021589342,0.00017028382,0.00030704646,0.00018190742,0.00019712016],"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":[0.0014044817,0.00023017348,0.46227375,0.0002656524,0.00044050408,0.0022435884,0.00031096794,0.0027626297,0.46196556,0.0006751366,0.00056864996,0.06685897],"study_design_scores_gemma":[0.000041117473,0.0010263922,0.8381593,0.00005104042,0.00034327005,0.008915499,0.0001847489,0.011507952,0.13441268,0.00034961355,0.004980898,0.000027420432],"about_ca_topic_score_codex":0.0007675433,"about_ca_topic_score_gemma":0.00129906,"teacher_disagreement_score":0.0019078319,"about_ca_system_score_codex":0.0001981789,"about_ca_system_score_gemma":0.00016920573,"threshold_uncertainty_score":0.010089695},"labels":[],"label_agreement":null},{"id":"W2024963499","doi":"10.1016/j.pedex.2011.04.003","title":"Isolated idiopathic bilateral vocal cord paralysis in two sisters: Case report and review of familial vocal cord paralysis","year":2011,"lang":"en","type":"article","venue":"International Journal of Pediatric Otorhinolaryngology Extra","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":3,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Children's Hospital of Eastern Ontario; University of Ottawa","funders":"","keywords":"Medicine; Paralysis; Cord; Vocal cord paralysis; Audiology; Surgery","score_opus":0.05285870551047246,"score_gpt":0.32088726881758434,"score_spread":0.2680285633071119,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2024963499","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":[0.77803636,0.18695895,0.0059436443,0.004855736,0.0023884466,0.00024693867,0.00058768305,0.00029285328,0.02068937],"genre_scores_gemma":[0.94436336,0.042150017,0.0026040645,0.002487086,0.0035337799,0.000071453884,0.00041918753,0.000062985586,0.0043080864],"study_design_codex":"case_report","study_design_gemma":"case_report","domain_scores_codex":[0.99918336,0.00010017077,0.00025149423,0.00022789076,0.000096283315,0.00014093523],"domain_scores_gemma":[0.99869967,0.0006394225,0.00024844604,0.00008346651,0.00012477805,0.00020418769],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.000496629,0.001163434,0.0013717944,0.0025133013,0.00084716483,0.0012172821,0.0016653785,0.003590208,0.002190315],"category_scores_gemma":[0.002540758,0.00070932624,0.00067451247,0.0012133105,0.0013904587,0.0019182985,0.00096793444,0.0011315439,0.001452872],"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":[0.000026519427,0.000031587075,0.004690634,0.00018035858,0.000020856507,0.9867731,0.00025286523,0.000040404106,0.0010740568,0.00007186755,0.0006921233,0.0061457274],"study_design_scores_gemma":[0.0000074939753,0.00003188956,0.005375165,0.000039808652,0.000029748498,0.99213713,0.00021523391,0.000055923636,0.00022833311,0.00007080705,0.0017975314,0.000010988591],"about_ca_topic_score_codex":0.0012320763,"about_ca_topic_score_gemma":0.0013962408,"teacher_disagreement_score":0.003590208,"about_ca_system_score_codex":0.0005852166,"about_ca_system_score_gemma":0.00061027,"threshold_uncertainty_score":0.007327378},"labels":[],"label_agreement":null},{"id":"W2025257478","doi":"10.1016/j.apmr.2003.12.025","title":"Resistance training effectiveness in patients with charcot-marie-tooth disease: Recommendations for exercise prescription11No commercial party having a direct financial interest in the results of the research supporting this article has or will confer a benefit upon the authors(s) or upon any organization with which the author(s) is/are associated.","year":2004,"lang":"en","type":"article","venue":"Archives of Physical Medicine and Rehabilitation","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":88,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"McMaster University Medical Centre","funders":"","keywords":"Medicine; Strength training; Physical therapy; Isometric exercise; Lean body mass; Medical prescription; Rehabilitation; Activities of daily living; Resistance training; Exercise prescription; Placebo; Internal medicine; Body weight; Alternative medicine; Nursing","score_opus":0.07458289161968658,"score_gpt":0.32691852292528456,"score_spread":0.252335631305598,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2025257478","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":[0.4754872,0.26041558,0.012524872,0.17954968,0.004714963,0.0054384503,0.005191633,0.001049181,0.055628434],"genre_scores_gemma":[0.87004864,0.061571375,0.039363105,0.010860366,0.0019666106,0.005586373,0.0028571968,0.00012721166,0.007619155],"study_design_codex":"design_other","study_design_gemma":"observational","domain_scores_codex":[0.99671125,0.0014080546,0.0007445763,0.00016178,0.00076248357,0.00021183201],"domain_scores_gemma":[0.9938538,0.0034019984,0.0009952048,0.0001316032,0.0010031891,0.0006142518],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0053449566,0.0009644336,0.0023979053,0.0015022742,0.00087825954,0.0011685798,0.002107647,0.0030304773,0.00477312],"category_scores_gemma":[0.014889273,0.000366356,0.0013503637,0.0009867281,0.0004056111,0.0007711705,0.0004529622,0.0018674219,0.0013611568],"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":[0.013318577,0.0081711635,0.19019483,0.008615913,0.002133772,0.0013772398,0.00077223335,0.0053686523,0.0032814047,0.001613786,0.10318447,0.6619679],"study_design_scores_gemma":[0.014802674,0.013228775,0.8539455,0.02134349,0.0062679597,0.0016561133,0.0041328925,0.023201354,0.0030716332,0.0042082095,0.053757712,0.0003836593],"about_ca_topic_score_codex":0.006404392,"about_ca_topic_score_gemma":0.017453061,"teacher_disagreement_score":0.006404392,"about_ca_system_score_codex":0.0013361755,"about_ca_system_score_gemma":0.0022372205,"threshold_uncertainty_score":0.028267145},"labels":[],"label_agreement":null},{"id":"W2025324254","doi":"10.4021/jcgo.v1i2-3.37","title":"Pregnancy Complicated by Familial Dysautonomia Riley-Day Syndrome: A Case Report","year":2012,"lang":"en","type":"article","venue":"Journal of Clinical Gynecology and Obstetrics","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":0,"is_retracted":false,"has_abstract":true,"route_ca_aff":false,"route_ca_fund":false,"route_ca_venue":true,"route_about_ca":false,"ca_institutions":"","funders":"","keywords":"Familial dysautonomia; Dysautonomia; Medicine; Pediatrics; Pregnancy; Gestation; Multidisciplinary approach; Disease; Internal medicine","score_opus":0.0886782521209143,"score_gpt":0.36136307347924157,"score_spread":0.2726848213583273,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2025324254","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":[0.96199566,0.011991087,0.0049278974,0.0055398075,0.0009395061,0.0003268332,0.00020393354,0.00022572653,0.013849486],"genre_scores_gemma":[0.9905033,0.0036961623,0.0016636132,0.0010221215,0.0013306265,0.00006548262,0.000080938546,0.000026784102,0.0016108862],"study_design_codex":"case_report","study_design_gemma":"case_report","domain_scores_codex":[0.9989838,0.00018811609,0.000106602,0.0002309425,0.00014599129,0.00034448292],"domain_scores_gemma":[0.9982784,0.0006075696,0.00040321992,0.00015837808,0.000062015366,0.00049048534],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0005830542,0.0025811682,0.0012690924,0.0029355937,0.004044678,0.0019000736,0.0013729151,0.0062131463,0.0025272607],"category_scores_gemma":[0.004968906,0.0017370566,0.0012563027,0.001728445,0.0020929459,0.0020310285,0.0024301857,0.0038241642,0.0007808298],"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":[0.000013079261,0.000032295353,0.0019391158,0.000012354543,0.000006239347,0.9969894,0.00012326388,0.000029051418,0.00014099493,0.00008936459,0.000112022055,0.00051280117],"study_design_scores_gemma":[0.00000781289,0.0000418433,0.0014551097,0.0000084689855,0.0000075295206,0.9978988,0.00009552813,0.00007837625,0.00008616989,0.00007769678,0.00023475735,0.000007883777],"about_ca_topic_score_codex":0.00394983,"about_ca_topic_score_gemma":0.0041700047,"teacher_disagreement_score":0.0062131463,"about_ca_system_score_codex":0.0013424885,"about_ca_system_score_gemma":0.0011747534,"threshold_uncertainty_score":0.009740472},"labels":[],"label_agreement":null},{"id":"W2025405352","doi":"10.1016/s0887-8994(02)00376-4","title":"A novel chronic childhood sensory predominant neuropathy","year":2002,"lang":"en","type":"article","venue":"Pediatric Neurology","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":6,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Montreal Children's Hospital; McGill University","funders":"","keywords":"Medicine; Hypotonia; Pediatrics; Cousin; Hereditary motor and sensory neuropathy; Audiology; Pathology","score_opus":0.030842980813787595,"score_gpt":0.22171571111342453,"score_spread":0.19087273029963694,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2025405352","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":[0.93985456,0.004181467,0.0044614584,0.0036163,0.00050236547,0.00020882227,0.0013071602,0.0003355014,0.045532368],"genre_scores_gemma":[0.9905476,0.0011043312,0.00217081,0.0008739245,0.00037332205,0.000034853983,0.00030907072,0.00006513681,0.0045209033],"study_design_codex":"case_report","study_design_gemma":"case_report","domain_scores_codex":[0.99925643,0.000047816255,0.00006082776,0.00017516299,0.00009521013,0.0003645519],"domain_scores_gemma":[0.9979348,0.0005783846,0.00046880168,0.00019532761,0.00024576587,0.0005768639],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0003210225,0.0016497556,0.0010065358,0.0018531564,0.0029149267,0.0016500446,0.0013579477,0.0034581972,0.007946008],"category_scores_gemma":[0.0021933373,0.00060591777,0.00070795766,0.002293291,0.0022330626,0.0020106062,0.0013809772,0.0026533108,0.0012367341],"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":[0.000075824435,0.000034090775,0.0068843435,0.000059412974,0.000010688436,0.9876695,0.00008386814,0.00009315729,0.0016502755,0.00081838935,0.00047096718,0.0021494697],"study_design_scores_gemma":[0.000023288478,0.00010209152,0.009478232,0.000018775634,0.000025910991,0.9878363,0.00015282552,0.00026672668,0.00093354326,0.00030620347,0.00084606267,0.000010094481],"about_ca_topic_score_codex":0.0082365265,"about_ca_topic_score_gemma":0.012221578,"teacher_disagreement_score":0.0082365265,"about_ca_system_score_codex":0.0021896856,"about_ca_system_score_gemma":0.0021530637,"threshold_uncertainty_score":0.026582062},"labels":[],"label_agreement":null},{"id":"W2027938923","doi":"10.1086/510782","title":"Mutations in the KIAA0196 Gene at the SPG8 Locus Cause Hereditary Spastic Paraplegia","year":2006,"lang":"en","type":"article","venue":"The American Journal of Human Genetics","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":192,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"McGill University; Children's & Women's Health Centre of British Columbia; Université de Montréal; Hôpital Notre-Dame","funders":"Wellcome Trust","keywords":"Hereditary spastic paraplegia; Locus (genetics); Genetics; Biology; Gene; Phenotype","score_opus":0.033143273342913226,"score_gpt":0.28210750107694493,"score_spread":0.2489642277340317,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2027938923","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":[0.9965402,0.00027915995,0.0007035423,0.0002660828,0.000032342672,0.000010243267,0.00025434635,0.00007663272,0.0018375487],"genre_scores_gemma":[0.9980573,0.00012519551,0.00048693194,0.000041899664,0.000023599712,0.000004933328,0.00019970197,0.000013613665,0.001046898],"study_design_codex":"case_report","study_design_gemma":"observational","domain_scores_codex":[0.9998791,0.000017026452,0.00001861748,0.000020156034,0.000045766006,0.000019317104],"domain_scores_gemma":[0.99971217,0.00006680266,0.00009742569,0.000014566788,0.000029200348,0.000079773796],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00010159689,0.0010488759,0.0003658597,0.0008188745,0.00042832358,0.00025000863,0.00037098452,0.0008448601,0.0028726743],"category_scores_gemma":[0.00054473564,0.00020469613,0.000259354,0.0006954144,0.00054499786,0.00021457797,0.00050427415,0.0005024234,0.00084776204],"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":[0.0017636996,0.00041044055,0.11624764,0.00025575506,0.00029805902,0.43912867,0.0007240887,0.0015567443,0.39492616,0.0026755321,0.004646842,0.037366446],"study_design_scores_gemma":[0.0005134181,0.0009644748,0.37080443,0.00009816237,0.0003435088,0.5328605,0.0008217479,0.004725722,0.07597308,0.003905663,0.0089027155,0.000086501845],"about_ca_topic_score_codex":0.0010251827,"about_ca_topic_score_gemma":0.0013672509,"teacher_disagreement_score":0.0028726743,"about_ca_system_score_codex":0.00031510327,"about_ca_system_score_gemma":0.00020000678,"threshold_uncertainty_score":0.009610057},"labels":[],"label_agreement":null},{"id":"W2032072524","doi":"10.1002/mus.21145","title":"Novel 95G&gt;A (R32K) somatic mosaic connexin 32 mutation","year":2008,"lang":"en","type":"article","venue":"Muscle & Nerve","topic":"Hereditary Neurological Disorders","field":"Neuroscience","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":"London Health Sciences Centre; Western University; McMaster University Medical Centre","funders":"","keywords":"Connexin 32; Mutation; Phenotype; Genetics; Transition (genetics); Biology; Somatic cell; Peripheral neuropathy; Gene; Lineage (genetic); Connexin; Endocrinology","score_opus":0.06605897500435143,"score_gpt":0.25446511795873267,"score_spread":0.18840614295438124,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2032072524","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":[0.99118584,0.00067723874,0.0011795686,0.0008873004,0.0001340904,0.000055212473,0.00056146993,0.00011766849,0.0052015404],"genre_scores_gemma":[0.9976566,0.00013974082,0.000523757,0.00017410125,0.00006543165,0.0000100678835,0.0001226081,0.000014996826,0.0012926827],"study_design_codex":"case_report","study_design_gemma":"case_report","domain_scores_codex":[0.9997696,0.000018828247,0.000018040295,0.00008886352,0.00005337486,0.00005127305],"domain_scores_gemma":[0.99964535,0.00009056639,0.00008280768,0.000014260268,0.000019667854,0.00014730185],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00016456554,0.0012009089,0.0004949308,0.0007090458,0.0007706125,0.00044807632,0.0006291032,0.0015933135,0.0025831282],"category_scores_gemma":[0.00079268264,0.00027324035,0.00041287858,0.0005647452,0.00088130124,0.0003616137,0.0005398258,0.0007477408,0.0006375663],"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":[0.00008027687,0.00005575331,0.004405863,0.000035153647,0.000022432687,0.970842,0.00031798513,0.00020269676,0.019594032,0.00072944287,0.00083426945,0.0028800298],"study_design_scores_gemma":[0.00004277097,0.00019366294,0.0193286,0.000021248556,0.000030075349,0.97438115,0.00012364547,0.00051949813,0.0033190397,0.0003371077,0.001680933,0.000022373068],"about_ca_topic_score_codex":0.0025872495,"about_ca_topic_score_gemma":0.0026718278,"teacher_disagreement_score":0.0025872495,"about_ca_system_score_codex":0.0005786868,"about_ca_system_score_gemma":0.00042376638,"threshold_uncertainty_score":0.008641362},"labels":[],"label_agreement":null},{"id":"W2033051292","doi":"10.1097/icl.0b013e3181f57aed","title":"Piggyback Cosmetic Contact Lens as an Occlusion Therapy in a Patient With Familial Dysautonomia","year":2010,"lang":"en","type":"article","venue":"Eye & Contact Lens Science & Clinical Practice","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":9,"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","funders":"","keywords":"Medicine; Contact lens; Familial dysautonomia; Optometry; Ophthalmology; Cornea; Lens (geology); Optics","score_opus":0.06300754724528126,"score_gpt":0.38107197188558295,"score_spread":0.3180644246403017,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2033051292","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":[0.9857943,0.0034798677,0.0012895511,0.0020494158,0.00018968961,0.000041087744,0.000053437812,0.00010998713,0.006992657],"genre_scores_gemma":[0.99566805,0.0007750536,0.0007631725,0.00061232515,0.00015815947,0.000009411338,0.000027664048,0.000020020752,0.0019659908],"study_design_codex":"case_report","study_design_gemma":"case_report","domain_scores_codex":[0.99967563,0.00004447461,0.00004246777,0.00006716126,0.0000705025,0.00009974546],"domain_scores_gemma":[0.9993105,0.0002035372,0.00019290722,0.00003118339,0.000029788618,0.00023218336],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00022626389,0.00097620895,0.00082295545,0.0013402234,0.002012852,0.0007020744,0.0005294502,0.0025091723,0.0017223335],"category_scores_gemma":[0.0015794721,0.0005186418,0.0007458285,0.00069761084,0.0009610911,0.0007554232,0.0006716544,0.0016070497,0.0003014757],"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":[0.000017006632,0.00001807252,0.003397286,0.000011166238,0.0000033785088,0.9948329,0.00019155852,0.000026469192,0.00062450586,0.000074625365,0.00008161704,0.0007214077],"study_design_scores_gemma":[0.0000036736249,0.00006433394,0.002501264,0.0000054328807,0.0000060666052,0.9967278,0.00009367963,0.000089086585,0.00022386754,0.000033880013,0.00024661387,0.000004216723],"about_ca_topic_score_codex":0.0028537484,"about_ca_topic_score_gemma":0.0049324166,"teacher_disagreement_score":0.0028537484,"about_ca_system_score_codex":0.0010029199,"about_ca_system_score_gemma":0.0007452186,"threshold_uncertainty_score":0.0072767735},"labels":[],"label_agreement":null},{"id":"W2036882358","doi":"10.1016/j.bbr.2010.12.022","title":"Sensorimotor and cognitive function of a NEFLP22S mutant model of Charcot–Marie–Tooth disease type 2E","year":2010,"lang":"en","type":"article","venue":"Behavioural Brain Research","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":21,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Université de Montréal; Université Laval","funders":"Canadian Institutes of Health Research","keywords":"Neuroscience; Genetically modified mouse; Transgene; Neurofilament; Hindlimb; Atrophy; Muscle atrophy; Pathogenesis; Mutation; Biology; Medicine; Anatomy; Gene; Internal medicine; Genetics","score_opus":0.1833883703191308,"score_gpt":0.37616759497062957,"score_spread":0.19277922465149877,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2036882358","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":[0.9966229,0.00021444412,0.0008546108,0.00027543417,0.0000758265,0.00003246186,0.00078080286,0.000103481856,0.0010400147],"genre_scores_gemma":[0.9912744,0.0002822558,0.0011380431,0.00012672655,0.000026235559,0.00011280594,0.00047863787,0.00008537042,0.0064755008],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99960643,0.000085208216,0.000043044627,0.00009048639,0.00009517074,0.00007963379],"domain_scores_gemma":[0.99925333,0.00017311002,0.00013311557,0.00006958742,0.00006863792,0.0003022192],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0004315659,0.0018669091,0.0008431817,0.0019386387,0.0007861246,0.0005076274,0.00090559456,0.0018076822,0.0052020536],"category_scores_gemma":[0.0006367156,0.00047240546,0.0007052449,0.00046885223,0.0015754286,0.0005039323,0.00060355145,0.0018976477,0.00068172574],"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":[0.0035552178,0.0015541916,0.00074468664,0.00006593067,0.00008666712,0.0031239912,0.00018090337,0.0010815703,0.9856629,0.0005054509,0.0007683816,0.0026700739],"study_design_scores_gemma":[0.002110781,0.010944914,0.042774964,0.00014011745,0.0006198883,0.013199411,0.000928192,0.02374532,0.8961714,0.0019739924,0.007098729,0.00029232242],"about_ca_topic_score_codex":0.00615075,"about_ca_topic_score_gemma":0.004832085,"teacher_disagreement_score":0.00615075,"about_ca_system_score_codex":0.0009858195,"about_ca_system_score_gemma":0.0006238581,"threshold_uncertainty_score":0.01740259},"labels":[],"label_agreement":null},{"id":"W2038389999","doi":"10.1038/npp.2012.241","title":"White Matter Abnormalities in Skin Picking Disorder: A Diffusion Tensor Imaging Study","year":2012,"lang":"en","type":"article","venue":"Neuropsychopharmacology","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":80,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Western University","funders":"","keywords":"Diffusion MRI; White matter; Psychology; Medicine; Neuroscience; Magnetic resonance imaging; Radiology","score_opus":0.019618582582060874,"score_gpt":0.29906671027061094,"score_spread":0.27944812768855004,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2038389999","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":[0.9988079,0.00008438265,0.0001073221,0.00006895878,0.0000073397246,0.00001741303,0.00007800042,0.0000049789396,0.0008236731],"genre_scores_gemma":[0.99938273,0.00008212046,0.00015095307,0.00005259058,0.000019260211,0.000004464933,0.00006212833,0.000005130659,0.00024058226],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9998203,0.000024012941,0.000028782544,0.000047380097,0.00002980518,0.000049863847],"domain_scores_gemma":[0.9995005,0.00011741934,0.000103132326,0.00004186021,0.00006657003,0.00017036611],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00041790077,0.0009978204,0.00041699028,0.0014838503,0.0011350932,0.0004735685,0.0005858871,0.000861725,0.0029696557],"category_scores_gemma":[0.0014455856,0.00048854796,0.00038317507,0.0008087507,0.0010797246,0.00084014336,0.0004963836,0.0006594229,0.00042824418],"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":[0.0030720155,0.0015042236,0.47105792,0.000159216,0.00024110584,0.42091474,0.002258347,0.0003770805,0.090688355,0.0003916737,0.00059303205,0.008742246],"study_design_scores_gemma":[0.00013188361,0.0010759671,0.79258466,0.00002079223,0.00023217502,0.19695646,0.0013088214,0.000662304,0.0060991324,0.0003723535,0.00051410566,0.000041441872],"about_ca_topic_score_codex":0.0062203486,"about_ca_topic_score_gemma":0.004869924,"teacher_disagreement_score":0.0062203486,"about_ca_system_score_codex":0.00040870628,"about_ca_system_score_gemma":0.0004953888,"threshold_uncertainty_score":0.012368262},"labels":[],"label_agreement":null},{"id":"W2041191850","doi":"10.1523/jneurosci.4633-08.2009","title":"Carriers of Recessive<i>WNK1</i>/<i>HSN2</i>Mutations for Hereditary Sensory and Autonomic Neuropathy Type 2 (HSAN2) Are More Sensitive to Thermal Stimuli","year":2009,"lang":"en","type":"article","venue":"Journal of Neuroscience","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":17,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Centre Hospitalier de l’Université de Montréal; McGill University","funders":"National Institute of Neurological Disorders and Stroke; National Institute of Dental and Craniofacial Research; Canadian Institutes of Health Research","keywords":"Sensory system; Neuroscience; Autonomic neuropathy; Sensory neuropathy; Medicine; Genetics; Psychology; Biology; Internal medicine","score_opus":0.04593135136145266,"score_gpt":0.30551170504880754,"score_spread":0.2595803536873549,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2041191850","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":[0.99961865,0.00005448412,0.00012822387,0.0000042426877,0.0000037606878,0.000004377173,0.000037684338,0.0000077608665,0.00014078365],"genre_scores_gemma":[0.9993284,0.00003435843,0.00023513829,0.000010191407,0.0000063294005,0.000005250651,0.000090331814,0.00000531374,0.00028477333],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99975926,0.000039329105,0.000023611814,0.000082056176,0.000060886698,0.000034919372],"domain_scores_gemma":[0.999653,0.000049492064,0.00018873769,0.000018599092,0.000030272999,0.000059951857],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00020976826,0.0007465606,0.00029256448,0.00068874983,0.00024650767,0.00022745221,0.00013762194,0.00023751093,0.0025555417],"category_scores_gemma":[0.0008565468,0.00018567313,0.00022666053,0.00018870062,0.00029919218,0.00016784485,0.00024265748,0.00020122468,0.00022310897],"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":[0.0029364107,0.0005321132,0.53943956,0.00013233564,0.0003494193,0.0064024813,0.00078037055,0.0002820308,0.43297857,0.00026528098,0.00053270574,0.015368685],"study_design_scores_gemma":[0.000050468563,0.0016438562,0.96583897,0.000015226449,0.00015306956,0.015720349,0.0002329449,0.00062417105,0.014763817,0.00009365186,0.0008332982,0.000030302097],"about_ca_topic_score_codex":0.0013322232,"about_ca_topic_score_gemma":0.0013722988,"teacher_disagreement_score":0.0025555417,"about_ca_system_score_codex":0.00010723477,"about_ca_system_score_gemma":0.000078862395,"threshold_uncertainty_score":0.008549154},"labels":[],"label_agreement":null},{"id":"W2041849406","doi":"10.1093/hmg/ddm272","title":"Disruption of neurofilament network with aggregation of light neurofilament protein: a common pathway leading to motor neuron degeneration due to Charcot–Marie–Tooth disease-linked mutations in NFL and HSPB1","year":2007,"lang":"en","type":"article","venue":"Human Molecular Genetics","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":116,"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 Laval","funders":"National Institutes of Health; University of Toronto; Muscular Dystrophy Association","keywords":"Mutant; Motor neuron; Neurofilament; Biology; Cell biology; Mutant protein; Protein aggregation; Wild type; Neuroscience; Biochemistry; Gene; Immunology; Immunohistochemistry","score_opus":0.023788420525032942,"score_gpt":0.26450966357180167,"score_spread":0.24072124304676873,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2041849406","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":[0.99726176,0.00086665526,0.0011395626,0.000047415728,0.000011682001,0.000026900612,0.000097562806,0.0000640837,0.00048440133],"genre_scores_gemma":[0.9969483,0.00052116875,0.00124079,0.000045419984,0.0000044685735,0.000035188805,0.00030986313,0.0000094900515,0.0008852655],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99984264,0.000021730855,0.000018915887,0.000035166588,0.000051579216,0.00002986839],"domain_scores_gemma":[0.999856,0.0000066366442,0.00006330427,0.0000114243485,0.000009853872,0.000052733387],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00013096197,0.00072881154,0.00028569167,0.0003863101,0.0002758805,0.00021391263,0.00017363469,0.000473074,0.00046699052],"category_scores_gemma":[0.00010432778,0.00024401725,0.00047781537,0.00018735584,0.0003020315,0.0002343002,0.00033586303,0.0004220478,0.00020167147],"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":[0.00004946486,0.000029252844,0.0006199791,0.000035151686,0.000011835042,0.00059663283,0.000012396277,0.000044033906,0.99815685,0.00005555324,0.000024918956,0.00036399887],"study_design_scores_gemma":[0.00005849903,0.0006953604,0.09583073,0.00003239358,0.000079596546,0.015739692,0.00009248079,0.0021900046,0.8823015,0.0002734795,0.0026863466,0.00001990954],"about_ca_topic_score_codex":0.0011373585,"about_ca_topic_score_gemma":0.0020614758,"teacher_disagreement_score":0.0011373585,"about_ca_system_score_codex":0.000574232,"about_ca_system_score_gemma":0.0002418221,"threshold_uncertainty_score":0.0041663647},"labels":[],"label_agreement":null},{"id":"W2042062226","doi":"10.2340/16501977-0143","title":"Manual dexterity in hereditary motor and sensory neuropathy type 1a: Severity of limitations and feasibility and reliability of 2 assessment instruments","year":2008,"lang":"en","type":"article","venue":"Acta Dermato Venereologica","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":31,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Institute of Infection and Immunity","funders":"","keywords":"Intraclass correlation; Physical medicine and rehabilitation; Medicine; Quantitative sensory testing; Reliability (semiconductor); Physical therapy; Confidence interval; Functional movement; Test (biology); Correlation; Audiology; Psychology; Sensory system; Psychometrics; Internal medicine; Mathematics; Clinical psychology","score_opus":0.07671499791258361,"score_gpt":0.2962951592835789,"score_spread":0.21958016137099529,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2042062226","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":[0.9995234,0.0001686204,0.00009387386,0.000009018351,0.0000034810614,0.000010717936,0.000056717723,0.0000022392858,0.00013193757],"genre_scores_gemma":[0.9994331,0.0000627065,0.00025538824,0.000008817454,0.0000074232703,0.000021195428,0.00013874746,0.000001047123,0.0000716046],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9976472,0.0010076473,0.00028242802,0.0003236899,0.00058731233,0.00015174251],"domain_scores_gemma":[0.9904293,0.0042823465,0.003493103,0.0002820566,0.0010538806,0.00045944116],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.005805022,0.00066033605,0.00044938037,0.0013696345,0.00023729724,0.00051679957,0.00047500254,0.0007485763,0.0011158038],"category_scores_gemma":[0.014048845,0.00040499732,0.00039085082,0.0006755647,0.0005477864,0.00072682335,0.00077311887,0.0004262426,0.00024292692],"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":[0.000161249,0.00006394924,0.9971215,0.000016209675,0.000048489615,0.000030753843,0.00011311133,0.000046180063,0.00019418017,0.0000046042355,0.00002419765,0.0021755064],"study_design_scores_gemma":[0.000011935795,0.00050724176,0.998727,0.00000980139,0.000018310864,0.00024450955,0.00012429165,0.0002444918,0.00006544178,0.000010117554,0.0000323872,0.000004363495],"about_ca_topic_score_codex":0.002097035,"about_ca_topic_score_gemma":0.0023814193,"teacher_disagreement_score":0.005805022,"about_ca_system_score_codex":0.00028289907,"about_ca_system_score_gemma":0.0002693646,"threshold_uncertainty_score":0.030700207},"labels":[],"label_agreement":null},{"id":"W2042145882","doi":"10.3389/fneur.2013.00098","title":"Venocentric Lesions: An MRI Marker of MS?","year":2013,"lang":"en","type":"article","venue":"Frontiers in Neurology","topic":"Hereditary Neurological Disorders","field":"Neuroscience","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":"Robarts Clinical Trials; Western University","funders":"Canadian Institutes of Health Research; Canada Research Chairs","keywords":"Magnetic resonance imaging; Medicine; Neuroscience; Psychology; Radiology","score_opus":0.01804073933171403,"score_gpt":0.23605388204704464,"score_spread":0.21801314271533062,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2042145882","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":[0.8197469,0.12624183,0.012571956,0.010232753,0.000756362,0.00009905645,0.00043516106,0.000340158,0.02957576],"genre_scores_gemma":[0.9806358,0.012754188,0.004013398,0.0005790229,0.00067776395,0.000011631789,0.00008543473,0.000019640112,0.0012231532],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9996867,0.00009483436,0.000029859006,0.0000631997,0.000073347685,0.00005210846],"domain_scores_gemma":[0.9990758,0.00026025894,0.0003062885,0.0000975624,0.00014013778,0.00011991571],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0008984058,0.0003777641,0.0007501778,0.0014936905,0.00020880922,0.0010362436,0.0005180274,0.0011794639,0.0015319524],"category_scores_gemma":[0.0024785802,0.00020576555,0.00013814562,0.00087178836,0.0008482327,0.0010668372,0.00030396954,0.0007517321,0.0005627984],"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":[0.002365424,0.00019908923,0.5221365,0.0014995725,0.00035606185,0.03345414,0.00062334497,0.00067748816,0.11647841,0.0059661786,0.0072198315,0.3090239],"study_design_scores_gemma":[0.00008205919,0.0014783358,0.58777434,0.0012741463,0.00043473527,0.32051235,0.0015986634,0.0035248753,0.035011243,0.014184227,0.033975665,0.00014934351],"about_ca_topic_score_codex":0.0007405695,"about_ca_topic_score_gemma":0.00063248194,"teacher_disagreement_score":0.0015319524,"about_ca_system_score_codex":0.0002148398,"about_ca_system_score_gemma":0.00018770737,"threshold_uncertainty_score":0.0051249266},"labels":[],"label_agreement":null},{"id":"W2043714441","doi":"10.1172/jci60560","title":"Mutations in the ER-shaping protein reticulon 2 cause the axon-degenerative disorder hereditary spastic paraplegia type 12","year":2012,"lang":"en","type":"article","venue":"Journal of Clinical Investigation","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":170,"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; Cambridge Institute for Medical Research, University of Cambridge; National Institutes of Health; Canada Excellence Research Chairs, Government of Canada; University of Miami; E-Rare; Spastic Paraplegia Foundation; Leonard M. Miller School of Medicine; Wellcome Trust; European Commission","keywords":"Hereditary spastic paraplegia; Frameshift mutation; Biology; Genetics; Mutation; Mutant protein; Gene; Cell biology; Phenotype","score_opus":0.23684033973893093,"score_gpt":0.39066549867703915,"score_spread":0.15382515893810822,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2043714441","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":[0.99555737,0.000717828,0.0011402973,0.00013117738,0.000035923378,0.000051904008,0.0004506268,0.00017702034,0.0017378024],"genre_scores_gemma":[0.9959247,0.00037016638,0.0013927736,0.00011917018,0.000028574968,0.000020984537,0.0004888335,0.00003113333,0.0016235353],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99980253,0.000037134003,0.000018064338,0.000059097405,0.000055984325,0.000027183496],"domain_scores_gemma":[0.9998418,0.000025813688,0.000058987,0.000009023943,0.000011297715,0.000052994237],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00013726155,0.0018403139,0.00038731453,0.00063875143,0.0002870831,0.00017866406,0.0003226816,0.0006646202,0.0015612801],"category_scores_gemma":[0.00039296862,0.00031423778,0.0002916427,0.00035794682,0.00037238502,0.000113697024,0.00046698918,0.0003628162,0.0005672351],"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":[0.0014365034,0.00024831574,0.04224797,0.00036764823,0.00040112663,0.091543764,0.00048443605,0.0008766606,0.83333373,0.0006661698,0.0026495007,0.025744198],"study_design_scores_gemma":[0.000599602,0.0017875732,0.48901173,0.00019499542,0.0005833445,0.33980814,0.00040179968,0.0047162287,0.14267854,0.0008325122,0.019284956,0.00010057818],"about_ca_topic_score_codex":0.0009656584,"about_ca_topic_score_gemma":0.0017122215,"teacher_disagreement_score":0.0018403139,"about_ca_system_score_codex":0.00042083228,"about_ca_system_score_gemma":0.00020949722,"threshold_uncertainty_score":0.005223036},"labels":[],"label_agreement":null},{"id":"W2043742507","doi":"10.1017/s0317167100001347","title":"PROGRESS IN CLINICAL NEUROSCIENCES: Charcot-Marie-Tooth Disease and Related Inherited Peripheral Neuropathies","year":2001,"lang":"en","type":"review","venue":"Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":18,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":true,"route_about_ca":false,"ca_institutions":"Health Sciences Centre; Queen Elizabeth II Health Sciences Centre; Dalhousie University","funders":"","keywords":"Tooth disease; Disease; Neuroscience; Medicine; Pathological; Genetic testing; Peripheral neuropathy; Bioinformatics; Pathology; Psychology; Biology; Internal medicine","score_opus":0.0984990223529485,"score_gpt":0.3464723773002908,"score_spread":0.2479733549473423,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2043742507","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":[0.00013605885,0.99715155,0.00013889778,0.00039690183,0.0004252987,0.000002751286,0.000004441873,0.0000107206215,0.0017334388],"genre_scores_gemma":[0.001343794,0.99609923,0.00029074252,0.00046628268,0.00062742794,0.0000049420473,0.000016264437,0.000002491294,0.001148705],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.999564,0.0000919546,0.00006132078,0.00006551424,0.00018074371,0.000036416244],"domain_scores_gemma":[0.9993088,0.0002900566,0.00007826149,0.000026379383,0.00021292636,0.000083594714],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00094852096,0.0012576412,0.0018642783,0.003725112,0.0005760174,0.0015885805,0.0008721261,0.0016893316,0.002622476],"category_scores_gemma":[0.001326683,0.00025323025,0.00039407922,0.004265919,0.00094806607,0.0024218007,0.00075805106,0.001966392,0.0030387985],"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":[0.000049520626,0.0000751916,0.0005557825,0.007918833,0.00005715711,0.001280747,0.000170699,0.00026242397,0.0009074151,0.0033999637,0.0541278,0.9311945],"study_design_scores_gemma":[0.000021491334,0.000068339185,0.002478328,0.0037369889,0.000068609865,0.015569466,0.00028277762,0.00009763284,0.00023651775,0.0036269668,0.9737853,0.00002763455],"about_ca_topic_score_codex":0.002152868,"about_ca_topic_score_gemma":0.004334705,"teacher_disagreement_score":0.003725112,"about_ca_system_score_codex":0.0010899615,"about_ca_system_score_gemma":0.0014152081,"threshold_uncertainty_score":0.008773088},"labels":[],"label_agreement":null},{"id":"W2043870528","doi":"10.1159/000185814","title":"Charcot-Marie-Tooth Disease and Nephropathy in a Mother and Daughter with a Review of the Literature","year":2008,"lang":"en","type":"review","venue":"The Nephron journals/Nephron journals","topic":"Hereditary Neurological Disorders","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":"Memorial University of Newfoundland","funders":"","keywords":"Medicine; Daughter; Nephropathy; Proteinuria; Disease; Internal medicine; Endocrinology; Kidney; Diabetes mellitus","score_opus":0.043730834435113115,"score_gpt":0.3056890265196876,"score_spread":0.2619581920845745,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2043870528","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":[0.001422399,0.99692816,0.00009510304,0.00019488248,0.00023628958,0.0000059282015,0.000028269573,0.000010088049,0.0010788551],"genre_scores_gemma":[0.008683168,0.98955846,0.0003017359,0.00039650788,0.0003906336,0.000009385506,0.000060088467,0.0000024551598,0.0005975539],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.99964523,0.000052169547,0.00010413694,0.00007062269,0.00009951307,0.000028352488],"domain_scores_gemma":[0.9994593,0.00025316584,0.00014127858,0.000015850579,0.00007891081,0.000051424788],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00033553864,0.0009896264,0.0019693053,0.005102914,0.00043838538,0.0007824602,0.0011015376,0.0011788107,0.0021680126],"category_scores_gemma":[0.0011962462,0.00029866578,0.00043735647,0.0047978074,0.00051395915,0.0011683071,0.00048404696,0.00068104843,0.0011591071],"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":[0.00017397056,0.00017913763,0.0075137406,0.041792676,0.0004617855,0.13737135,0.0005475232,0.00058068964,0.0021188497,0.0014371817,0.061553143,0.74626994],"study_design_scores_gemma":[0.000040760984,0.00020748738,0.019505471,0.016954284,0.001003587,0.59392816,0.0010099589,0.00022160148,0.000630462,0.0015878454,0.36481848,0.00009191588],"about_ca_topic_score_codex":0.0018227336,"about_ca_topic_score_gemma":0.003294764,"teacher_disagreement_score":0.005102914,"about_ca_system_score_codex":0.00046547587,"about_ca_system_score_gemma":0.0009378832,"threshold_uncertainty_score":0.007252693},"labels":[],"label_agreement":null},{"id":"W2045656807","doi":"10.3109/00207454.2011.633719","title":"Hereditary Neuropathy with Liability to Pressure Palsy: A Brief Review with a Case Report","year":2011,"lang":"en","type":"review","venue":"International Journal of Neuroscience","topic":"Hereditary Neurological Disorders","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":false,"ca_institutions":"McMaster University","funders":"","keywords":"Mononeuropathy; Medicine; Palsy; Peripheral neuropathy; Asymptomatic; Disease; Peripheral myelin protein 22; Differential diagnosis; Myelin; Pathology; Internal medicine; Central nervous system; Endocrinology; Diabetes mellitus","score_opus":0.09000233536108285,"score_gpt":0.35343206948566946,"score_spread":0.2634297341245866,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2045656807","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":[0.0014933522,0.99276334,0.000616416,0.0006982457,0.0009777965,0.00002143149,0.000052317988,0.000030302292,0.0033468073],"genre_scores_gemma":[0.0053810985,0.989504,0.0007225139,0.0007468209,0.0018623521,0.000020119905,0.000109380904,0.000005833033,0.0016478493],"study_design_codex":"design_other","study_design_gemma":"case_report","domain_scores_codex":[0.9997433,0.000036843507,0.00006641483,0.00006237407,0.00006235396,0.000028767183],"domain_scores_gemma":[0.9997086,0.00011550595,0.000064100794,0.000011726019,0.00005211487,0.000047897232],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00030021253,0.001519376,0.0017323302,0.0053298944,0.00057879277,0.0010003666,0.0012341905,0.00178041,0.0040489426],"category_scores_gemma":[0.00069223746,0.0003545457,0.0006826834,0.004123332,0.0007406439,0.0022521259,0.0008314834,0.0013396428,0.0027953216],"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":[0.00013399367,0.0003534914,0.0024008423,0.018103419,0.00020091617,0.08977517,0.00040722382,0.0006966436,0.0026709284,0.0027163846,0.10589695,0.776644],"study_design_scores_gemma":[0.000029827503,0.0001999567,0.0058439504,0.004176929,0.00027166217,0.38306254,0.00043466175,0.00023981443,0.000598769,0.002465726,0.6025817,0.00009451583],"about_ca_topic_score_codex":0.0010894223,"about_ca_topic_score_gemma":0.001953919,"teacher_disagreement_score":0.0053298944,"about_ca_system_score_codex":0.00056399807,"about_ca_system_score_gemma":0.0007421959,"threshold_uncertainty_score":0.013545036},"labels":[],"label_agreement":null},{"id":"W2046401057","doi":"10.1111/j.1529-8027.2012.00374.x","title":"Expanding the differential diagnosis of inherited neuropathies with non‐uniform conduction: Andermann syndrome","year":2012,"lang":"en","type":"article","venue":"Journal of the Peripheral Nervous System","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":14,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Université de Montréal; Université Laval","funders":"","keywords":"Differential diagnosis; Medicine; Scoliosis; Ataxia; Corpus callosum; Pediatrics; Physical medicine and rehabilitation; Anatomy; Pathology; Surgery; Psychiatry","score_opus":0.02874628501244426,"score_gpt":0.240893981553036,"score_spread":0.21214769654059176,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2046401057","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":[0.9828928,0.005791004,0.0029082417,0.0010171494,0.00013618513,0.000058150883,0.00012555333,0.00016083436,0.006910101],"genre_scores_gemma":[0.99494815,0.0021121774,0.0017493641,0.00021744266,0.00018163407,0.000011968941,0.00007696203,0.000015253787,0.0006870505],"study_design_codex":"case_report","study_design_gemma":"case_report","domain_scores_codex":[0.9995896,0.00006303022,0.000073923744,0.00007777197,0.000070695045,0.00012503963],"domain_scores_gemma":[0.99929905,0.00024462552,0.00019143648,0.000041441144,0.00007413379,0.00014939206],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0004095948,0.0013565735,0.00063432916,0.0014704424,0.00055318524,0.00051146164,0.00058595586,0.001152301,0.001959508],"category_scores_gemma":[0.0025167416,0.00030210635,0.00017832928,0.0005209632,0.0005898898,0.0012744695,0.0008026478,0.00071657135,0.00043759108],"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":[0.00019173555,0.000049950042,0.06770445,0.00016263589,0.000023150616,0.90179396,0.00036564277,0.0001595147,0.0132642295,0.000463688,0.00066287984,0.015158197],"study_design_scores_gemma":[0.000035868023,0.00010765113,0.036474142,0.00008879046,0.000035942878,0.9571834,0.00028318135,0.00044617642,0.0029646007,0.0006369107,0.0017285132,0.000014737934],"about_ca_topic_score_codex":0.00085291284,"about_ca_topic_score_gemma":0.0011513387,"teacher_disagreement_score":0.001959508,"about_ca_system_score_codex":0.00023439695,"about_ca_system_score_gemma":0.00037017107,"threshold_uncertainty_score":0.0065551996},"labels":[],"label_agreement":null},{"id":"W2046425763","doi":"10.1002/ajmg.a.32456","title":"Compound heterozygous deletions of <i>PMP22</i> causing severe Charcot‐Marie‐Tooth disease of the Dejerine‐Sottas disease phenotype","year":2008,"lang":"en","type":"article","venue":"American Journal of Medical Genetics Part A","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":26,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"McGill University; Children's Hospital of Eastern Ontario; McGill University Health Centre; Montreal Children's Hospital","funders":"","keywords":"Compound heterozygosity; Genetics; Allele; Phenotype; Exon; Biology; Heterozygote advantage; Medicine; Gene","score_opus":0.03586543822340807,"score_gpt":0.2716284176725993,"score_spread":0.23576297944919125,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2046425763","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":[0.9950899,0.00060688163,0.0012320062,0.00010913799,0.00005841234,0.000052323798,0.0003743786,0.000088151144,0.0023888838],"genre_scores_gemma":[0.99762064,0.00035788567,0.0008850004,0.0000793822,0.00011391183,0.000020335729,0.0002582138,0.000032051994,0.0006325331],"study_design_codex":"case_report","study_design_gemma":"observational","domain_scores_codex":[0.99968135,0.00004435466,0.00003612238,0.00012183168,0.000056170644,0.000060274546],"domain_scores_gemma":[0.9993954,0.00015666326,0.00018396965,0.00002316586,0.000024750001,0.00021608706],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00015308068,0.0017396308,0.0007334715,0.0005435655,0.0005581141,0.00040357272,0.0003350015,0.0010451186,0.0018013872],"category_scores_gemma":[0.0006693546,0.00042361772,0.0003269375,0.00037652586,0.0007408836,0.00028114195,0.00061147107,0.0006377386,0.0006234783],"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":[0.0006587613,0.00023094505,0.042144172,0.00020627464,0.00017258295,0.7057938,0.00070912525,0.0006722683,0.23600198,0.00091915426,0.0018295358,0.010661452],"study_design_scores_gemma":[0.00012779974,0.0012918805,0.13032594,0.000041263724,0.00016350123,0.83374745,0.00025500625,0.000786299,0.02737659,0.0003435918,0.0054527186,0.000088058405],"about_ca_topic_score_codex":0.00090578175,"about_ca_topic_score_gemma":0.0013006217,"teacher_disagreement_score":0.0018013872,"about_ca_system_score_codex":0.00024387981,"about_ca_system_score_gemma":0.00026194297,"threshold_uncertainty_score":0.006026268},"labels":[],"label_agreement":null},{"id":"W204677643","doi":"10.1007/s004010000275","title":"Pathological findings in the x-linked form of Charcot-Marie-Tooth disease: a morphometric and ultrastructural analysis","year":2001,"lang":"en","type":"article","venue":"Acta Neuropathologica","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":90,"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; University of Toronto; London Health Sciences Centre; Western University","funders":"","keywords":"Schwann cell; Myelin; Axon; Biology; Connexin 32; Pathology; Hereditary motor and sensory neuropathy; Wallerian degeneration; Node of Ranvier; Ultrastructure; Sural nerve; Cytoplasm; Nerve biopsy; Neuroscience; Anatomy; Cell biology; Peripheral neuropathy; Gap junction; Genetics; Connexin; Medicine; Intracellular; Gene; Central nervous system","score_opus":0.03338205661409242,"score_gpt":0.2577461445839596,"score_spread":0.22436408796986718,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W204677643","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":[0.9932058,0.0020331908,0.0015135624,0.00006640272,0.000019983778,0.000021159074,0.00014619197,0.000042608932,0.0029511082],"genre_scores_gemma":[0.9948426,0.0010720178,0.0024114896,0.000030118617,0.000015116497,0.000019476833,0.00015523525,0.000014060647,0.0014399998],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.99984837,0.00002207374,0.000018803079,0.000023357446,0.000055813096,0.000031508516],"domain_scores_gemma":[0.99980086,0.00003672089,0.000044087006,0.000027344082,0.000050857736,0.000040109382],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00038631025,0.00034575173,0.00026038298,0.0011794032,0.0005838019,0.00039559725,0.00028446098,0.0006385673,0.00094132224],"category_scores_gemma":[0.0003943485,0.0004022292,0.00021467252,0.0005664177,0.0007707855,0.0005400782,0.00037247167,0.0003200016,0.00032382493],"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":[0.0014169278,0.0003208364,0.03908873,0.00043863032,0.00024648613,0.029269226,0.00068322266,0.0007569736,0.9098784,0.0025071432,0.0006188467,0.014774755],"study_design_scores_gemma":[0.000083438135,0.00073770504,0.7450281,0.00007036676,0.00024213931,0.16379346,0.00093100657,0.0031804733,0.07882352,0.001554268,0.0055060247,0.000049453047],"about_ca_topic_score_codex":0.00115702,"about_ca_topic_score_gemma":0.0013193388,"teacher_disagreement_score":0.0011794032,"about_ca_system_score_codex":0.00021455465,"about_ca_system_score_gemma":0.00016705434,"threshold_uncertainty_score":0.0031490922},"labels":[],"label_agreement":null},{"id":"W2048750982","doi":"10.1016/j.brainresbull.2012.05.003","title":"Molecular basis of axonal dysfunction and traffic impairments in CMT","year":2012,"lang":"en","type":"review","venue":"Brain Research Bulletin","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":54,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"McGill University; Montreal Neurological Institute and Hospital","funders":"Canadian Institutes of Health Research","keywords":"Phenotype; Gene; Biology; MFN2; Neuroscience; Disease; Genetics; Loss function; Axoplasmic transport; Pathogenesis; Cell biology; Medicine; Pathology; Immunology; Mitochondrial DNA; mitochondrial fusion","score_opus":0.18636962389943973,"score_gpt":0.4024675906386512,"score_spread":0.21609796673921144,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2048750982","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":[0.0002680671,0.9983139,0.00024891156,0.00023939303,0.00014028515,0.000004486043,0.00002735309,0.000010087477,0.00074758654],"genre_scores_gemma":[0.0010884785,0.9978483,0.0003010299,0.000102377206,0.00017205723,0.000005284544,0.000045887333,0.0000010323683,0.00043566054],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.99990666,0.000010265175,0.000019154622,0.00002244874,0.000028765082,0.000012718872],"domain_scores_gemma":[0.99984276,0.000059420618,0.00003272708,0.000006057597,0.000043567477,0.000015292455],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00037772182,0.0010990729,0.0013669273,0.0017193288,0.00023004872,0.00078573177,0.0009122647,0.0011569043,0.0017419719],"category_scores_gemma":[0.000428546,0.00026494949,0.00044322922,0.0016059154,0.00053986284,0.0010029199,0.00055980054,0.0013507073,0.0012006034],"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":[0.00018704725,0.00010024825,0.0005517368,0.011537905,0.0001305026,0.0015091825,0.00005240282,0.0007096802,0.0069582066,0.003710449,0.026134022,0.9484186],"study_design_scores_gemma":[0.000065534536,0.0001278977,0.004359168,0.0036402885,0.0005349617,0.009914761,0.00015141371,0.00036232048,0.0032340856,0.006274613,0.97126836,0.000066581095],"about_ca_topic_score_codex":0.0014987199,"about_ca_topic_score_gemma":0.0020031608,"teacher_disagreement_score":0.0017419719,"about_ca_system_score_codex":0.0006547721,"about_ca_system_score_gemma":0.00097375707,"threshold_uncertainty_score":0.0058274865},"labels":[],"label_agreement":null},{"id":"W2048953337","doi":"10.1111/j.1365-2443.2009.01320.x","title":"Conserved aromatic and basic amino acid residues in the pore region of <i>Caenorhabditis elegans</i> spastin play critical roles in microtubule severing","year":2009,"lang":"en","type":"article","venue":"Genes to Cells","topic":"Hereditary Neurological Disorders","field":"Neuroscience","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":"Core Research for Evolutional Science and Technology; Institute of Genetics; Japan Science and Technology Agency; Ministry of Education, Culture, Sports, Science and Technology","keywords":"Microtubule; AAA proteins; Random hexamer; Biology; Caenorhabditis elegans; Cell biology; Tubulin; ATPase; Biochemistry; Biophysics; Enzyme; Gene","score_opus":0.024491978509473197,"score_gpt":0.24528380667589592,"score_spread":0.22079182816642273,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2048953337","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":[0.9965687,0.00052187283,0.0018817565,0.000057713878,0.000026465581,0.000017273624,0.00016316723,0.00007378205,0.00068926346],"genre_scores_gemma":[0.99761945,0.00014414037,0.00129909,0.000052942698,0.0000073258893,0.000009147316,0.00029611835,0.000012504627,0.0005591482],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9999236,0.0000091433485,0.0000074270833,0.00002016266,0.000021275308,0.000018477453],"domain_scores_gemma":[0.99981946,0.000021896565,0.000063777145,0.000010238997,0.00001583213,0.000068764355],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00009022764,0.00032875504,0.00018094871,0.00013046054,0.00022892166,0.000165434,0.00019408838,0.0002801394,0.000836732],"category_scores_gemma":[0.00016550689,0.00011685893,0.00029333006,0.000079618854,0.00021968196,0.0001670811,0.0002027013,0.00038099667,0.00040778023],"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":[0.000100924684,0.000015513568,0.00039408373,0.000026617552,0.0000058149085,0.00022924715,0.000009505138,0.000082454935,0.998357,0.00007931301,0.000040114188,0.00065934233],"study_design_scores_gemma":[0.00006721314,0.0005540798,0.069372535,0.000037241873,0.00006882969,0.002534801,0.00006993894,0.0029092706,0.9192698,0.00025088916,0.0048306216,0.00003477865],"about_ca_topic_score_codex":0.0007690939,"about_ca_topic_score_gemma":0.0010045599,"teacher_disagreement_score":0.000836732,"about_ca_system_score_codex":0.0003236944,"about_ca_system_score_gemma":0.00019942885,"threshold_uncertainty_score":0.0027991533},"labels":[],"label_agreement":null},{"id":"W2049492077","doi":"10.1016/j.biocel.2013.04.009","title":"Heterogeneity in the properties of NEFL mutants causing Charcot–Marie–Tooth disease results in differential effects on neurofilament assembly and susceptibility to intervention by the chaperone-inducer, celastrol","year":2013,"lang":"en","type":"article","venue":"The International Journal of Biochemistry & Cell Biology","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":24,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"McGill University; Montreal Neurological Institute and Hospital","funders":"Canadian Institutes of Health Research; McGill University","keywords":"Celastrol; Mutant; Chaperone (clinical); Neurofilament; Inducer; Biology; Chemistry; Neuroscience; Genetics; Medicine; Immunology; Apoptosis; Gene; Pathology","score_opus":0.02421996737035844,"score_gpt":0.2685084481579824,"score_spread":0.24428848078762397,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2049492077","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":[0.99833906,0.00013774514,0.0006356913,0.000040498195,0.000011029793,0.000007577153,0.00029027907,0.000039247814,0.0004987528],"genre_scores_gemma":[0.99747986,0.00011222572,0.0007269755,0.000045679444,0.0000045823494,0.000017184082,0.0004644718,0.000078492536,0.0010703803],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99970955,0.000037659163,0.000057722937,0.000059352504,0.00006260634,0.00007316066],"domain_scores_gemma":[0.9994942,0.00010627075,0.00014278978,0.000048112543,0.000042722415,0.00016587396],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00021645674,0.00064332626,0.00031762445,0.0006968161,0.00026276064,0.00042700864,0.00039745533,0.00061691366,0.0016259738],"category_scores_gemma":[0.0004019837,0.0003222693,0.00047894192,0.00023375708,0.00047698012,0.0002893018,0.00047628494,0.000695764,0.0005591961],"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":[0.00009667268,0.000018195762,0.00018996527,0.000006138666,0.000007634892,0.000126479,0.000015041676,0.000033677927,0.99920696,0.000035332694,0.00001577064,0.00024814307],"study_design_scores_gemma":[0.00006419189,0.00026416744,0.03273079,0.000016071941,0.00007735189,0.0034410765,0.00015327394,0.0014947483,0.9598237,0.00019418316,0.0017031883,0.00003712779],"about_ca_topic_score_codex":0.0011834617,"about_ca_topic_score_gemma":0.0023155073,"teacher_disagreement_score":0.0016259738,"about_ca_system_score_codex":0.00043147334,"about_ca_system_score_gemma":0.00019636606,"threshold_uncertainty_score":0.0054394603},"labels":[],"label_agreement":null},{"id":"W2052098785","doi":"10.1093/brain/awu224","title":"A novel mutation in VCP causes Charcot–Marie–Tooth Type 2 disease","year":2014,"lang":"en","type":"article","venue":"Brain","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":144,"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":"Clinical and Translational Science Institute, University of California, Los Angeles; National Center for Advancing Translational Sciences; National Institute of Neurological Disorders and Stroke; Jonsson Comprehensive Cancer Center; Hope Center for Neurological Disorders; National Institute on Aging; National Institutes of Health; McMaster University; Muscular Dystrophy Association","keywords":"Tooth disease; Mutation; Disease; Genetics; Medicine; Biology; Pathology; Gene","score_opus":0.04281290399853393,"score_gpt":0.27689224655336275,"score_spread":0.23407934255482882,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2052098785","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":[0.99347514,0.0006750869,0.0012292559,0.0003313769,0.00021510755,0.000037896818,0.00023380162,0.00012408361,0.003678244],"genre_scores_gemma":[0.9981475,0.00014642446,0.0006179198,0.00009942966,0.000078190445,0.000010068747,0.000118660275,0.000014992634,0.00076687505],"study_design_codex":"case_report","study_design_gemma":"observational","domain_scores_codex":[0.99977905,0.000017825525,0.000023745039,0.000064388136,0.00007113373,0.000043877248],"domain_scores_gemma":[0.99970454,0.000086404725,0.000054206383,0.000011754567,0.000024570172,0.00011849873],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00018764171,0.0010903899,0.00044367817,0.0009272705,0.00077432406,0.0004629929,0.00047797617,0.0015259964,0.0017097342],"category_scores_gemma":[0.0008611009,0.00020339555,0.00033958803,0.0004883652,0.0005823111,0.00024339711,0.00066432037,0.00051519275,0.00045847526],"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":[0.00043107604,0.00017868466,0.017548328,0.00014375856,0.00010078041,0.82159024,0.0007096636,0.0005507986,0.14116481,0.0016815102,0.002592545,0.013307811],"study_design_scores_gemma":[0.00021352955,0.00039648544,0.097930156,0.000097844524,0.00015693967,0.8502097,0.0002759067,0.0027577663,0.035143197,0.0013067067,0.011416352,0.00009542485],"about_ca_topic_score_codex":0.0027532903,"about_ca_topic_score_gemma":0.0025663734,"teacher_disagreement_score":0.0027532903,"about_ca_system_score_codex":0.00071152113,"about_ca_system_score_gemma":0.0005310453,"threshold_uncertainty_score":0.005719602},"labels":[],"label_agreement":null},{"id":"W2052229179","doi":"10.1002/mds.20264","title":"Striking intrafamilial phenotypic variability and spastic paraplegia in the presence of similar homozygous expansions of the <i>FRDA1</i> gene","year":2004,"lang":"en","type":"review","venue":"Movement Disorders","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":21,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Université de Montréal; McGill University; Montreal Neurological Institute and Hospital","funders":"","keywords":"Paraplegia; Spastic; Phenotype; Hereditary spastic paraplegia; Genetics; Physical medicine and rehabilitation; Gene; Biology; Medicine; Neuroscience; Spinal cord; Cerebral palsy","score_opus":0.03658904447901533,"score_gpt":0.278554063619146,"score_spread":0.24196501914013063,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2052229179","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":[0.0007696037,0.99616075,0.00021020029,0.00021181395,0.000119767144,0.0000032618639,0.000014612151,0.000013766228,0.0024962008],"genre_scores_gemma":[0.0058006886,0.99166906,0.00043779798,0.00024238415,0.00019376975,0.000009156489,0.000053272204,0.000002589039,0.0015913254],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.9998715,0.000026350372,0.000019728253,0.000030308795,0.000038486025,0.000013584567],"domain_scores_gemma":[0.9998222,0.00007540721,0.00003206436,0.000008221257,0.000043469132,0.000018576533],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00033567045,0.00088858226,0.0012492934,0.0016768258,0.00020812168,0.0005858344,0.0005509844,0.00077221356,0.0018869198],"category_scores_gemma":[0.00043386844,0.00016864119,0.00018414661,0.0014710202,0.00034817698,0.0007771853,0.00032051213,0.0004979719,0.0017565984],"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":[0.000068984526,0.00003742395,0.0007649152,0.00507954,0.000061758,0.002844681,0.000080203456,0.0002198108,0.0019445299,0.0010373502,0.018057536,0.9698033],"study_design_scores_gemma":[0.000052134958,0.00020590359,0.009886456,0.002418455,0.00023785877,0.07194283,0.00022373654,0.00017669723,0.0013970652,0.0025897378,0.9108261,0.000042947137],"about_ca_topic_score_codex":0.0009951503,"about_ca_topic_score_gemma":0.0022200793,"teacher_disagreement_score":0.0018869198,"about_ca_system_score_codex":0.00033339797,"about_ca_system_score_gemma":0.0005095976,"threshold_uncertainty_score":0.00631243},"labels":[],"label_agreement":null},{"id":"W2052440546","doi":"10.1002/ana.20237","title":"A mutation in the <i>HSN2</i> gene causes sensory neuropathy type II in a Lebanese family","year":2004,"lang":"en","type":"article","venue":"Annals of Neurology","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":45,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":true,"ca_institutions":"Montreal Children's Hospital; McGill University","funders":"Canadian Institutes of Health Research","keywords":"Gene; Genetics; Sensory system; Mutation; Sensory neuropathy; Peripheral neuropathy; Biology; Medicine; Endocrinology; Internal medicine; Neuroscience","score_opus":0.13127169378512005,"score_gpt":0.32788171313875636,"score_spread":0.1966100193536363,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2052440546","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":[0.9967719,0.00020783482,0.000536136,0.00016559754,0.000020600935,0.000015131202,0.000120599485,0.000023039303,0.0021391995],"genre_scores_gemma":[0.9967187,0.00016335842,0.00066003966,0.0001964066,0.000020869453,0.000008011803,0.00014886426,0.00001763576,0.0020660022],"study_design_codex":"case_report","study_design_gemma":"observational","domain_scores_codex":[0.99989986,0.000014104873,0.0000071339314,0.000028349192,0.000022924925,0.000027587808],"domain_scores_gemma":[0.9998803,0.000019190556,0.000020591762,0.000005788758,0.000019075967,0.00005497524],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00013986582,0.00092118216,0.00025837222,0.00046787178,0.0011315887,0.0002772366,0.00030169447,0.00037197344,0.001933003],"category_scores_gemma":[0.00030618353,0.00017624194,0.00024872593,0.00030998807,0.0004785339,0.00010022511,0.0003498654,0.0003181266,0.00029021592],"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":[0.00071081036,0.00037266218,0.2385109,0.00012982624,0.00027412167,0.44031322,0.004565156,0.0005872057,0.26944363,0.0016284924,0.0047078757,0.038756076],"study_design_scores_gemma":[0.00020254651,0.0005895117,0.5887303,0.00009314784,0.0002433064,0.36724967,0.0018842581,0.0017299773,0.023921587,0.00034591235,0.014929876,0.00008002157],"about_ca_topic_score_codex":0.049168605,"about_ca_topic_score_gemma":0.06543438,"teacher_disagreement_score":0.049168605,"about_ca_system_score_codex":0.00083444914,"about_ca_system_score_gemma":0.0005437868,"threshold_uncertainty_score":0.09776485},"labels":[],"label_agreement":null},{"id":"W2053954502","doi":"10.1016/j.crad.2010.11.009","title":"MRI findings in X-linked Charcot–Marie–Tooth disease associated with a novel connexin 32 mutation","year":2011,"lang":"en","type":"review","venue":"Clinical Radiology","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":14,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"SickKids Foundation; Hospital for Sick Children; University of Toronto","funders":"","keywords":"Medicine; Tooth disease; Scopus; Connexin 32; Connexin; Natural history; Genetics; Disease; Pathology; Internal medicine; MEDLINE; Biology; Gap junction","score_opus":0.2330869065270455,"score_gpt":0.40115248952831295,"score_spread":0.16806558300126745,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2053954502","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":[0.006449888,0.9872853,0.000808743,0.000539142,0.00026143505,0.000014935259,0.00009030302,0.00004822439,0.0045020008],"genre_scores_gemma":[0.039144617,0.9558334,0.0013156689,0.00067943335,0.00080418447,0.000012822637,0.00025485773,0.000013293121,0.0019415892],"study_design_codex":"design_other","study_design_gemma":"observational","domain_scores_codex":[0.99980026,0.0000309017,0.000050713326,0.000050339262,0.00004674337,0.000021124579],"domain_scores_gemma":[0.9996891,0.00014794267,0.00007673892,0.000010478972,0.000047057507,0.000028731081],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0002649212,0.0012655569,0.0013375545,0.002614593,0.00016626708,0.0006494193,0.0010355051,0.0013854027,0.0014413696],"category_scores_gemma":[0.0006363128,0.0003491073,0.00042136238,0.0016055248,0.0006167458,0.0008640112,0.0004977837,0.0006929424,0.0009534304],"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":[0.00029525667,0.00010311221,0.0041557234,0.017449025,0.00045328526,0.22347628,0.00025777452,0.0010128013,0.021730445,0.00227261,0.036647055,0.6921466],"study_design_scores_gemma":[0.00009053182,0.0001254912,0.016861146,0.0035010527,0.000908927,0.7138801,0.0002496199,0.00056816556,0.0049709645,0.001497868,0.25721836,0.00012775292],"about_ca_topic_score_codex":0.00154463,"about_ca_topic_score_gemma":0.0022985,"teacher_disagreement_score":0.002614593,"about_ca_system_score_codex":0.00043689608,"about_ca_system_score_gemma":0.00057293114,"threshold_uncertainty_score":0.004821837},"labels":[],"label_agreement":null},{"id":"W2054792702","doi":"10.1017/s0317167100006053","title":"Possible Anticipation in Hereditary Spastic Paraplegia Type 4 (SPG4)","year":2007,"lang":"en","type":"article","venue":"Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":18,"is_retracted":false,"has_abstract":true,"route_ca_aff":false,"route_ca_fund":false,"route_ca_venue":true,"route_about_ca":false,"ca_institutions":"","funders":"","keywords":"Hereditary spastic paraplegia; Anticipation (artificial intelligence); Paraplegia; Medicine; Physical medicine and rehabilitation; Spastic; Genetics; Biology; Spinal cord; Computer science; Phenotype; Psychiatry; Artificial intelligence; Gene; Cerebral palsy","score_opus":0.06083120838453212,"score_gpt":0.30318792337811756,"score_spread":0.24235671499358544,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2054792702","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":[0.9976525,0.00031382957,0.0008051817,0.00019700668,0.000017344302,0.000009078275,0.000064614214,0.000039554492,0.00090084615],"genre_scores_gemma":[0.9982039,0.00016851861,0.0007186566,0.00005826642,0.000040654682,0.000008048434,0.000074983,0.0000069131775,0.0007199367],"study_design_codex":"case_report","study_design_gemma":"observational","domain_scores_codex":[0.9998272,0.00003835491,0.0000143622565,0.00004433385,0.00003774915,0.000037984635],"domain_scores_gemma":[0.99958676,0.00015914928,0.00014028343,0.000016034559,0.000026926427,0.00007085264],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00020771727,0.0014274877,0.00030234177,0.000815138,0.0007963516,0.00026587286,0.00043906335,0.0009966879,0.003603711],"category_scores_gemma":[0.0012775486,0.0002667735,0.0003773315,0.00045341754,0.00054772355,0.00030736893,0.0005897979,0.00057111913,0.0003716509],"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":[0.00047906055,0.00015975029,0.15931004,0.00012271933,0.00009011192,0.781453,0.00090135954,0.0009539534,0.04032004,0.00093827397,0.00086356635,0.014408204],"study_design_scores_gemma":[0.00008043348,0.0007520458,0.0992977,0.000058999227,0.00020344013,0.8818403,0.0003078058,0.0015021493,0.01136654,0.0013107058,0.003234879,0.000045015593],"about_ca_topic_score_codex":0.000962361,"about_ca_topic_score_gemma":0.0012147167,"teacher_disagreement_score":0.003603711,"about_ca_system_score_codex":0.00024903586,"about_ca_system_score_gemma":0.00033268039,"threshold_uncertainty_score":0.012055576},"labels":[],"label_agreement":null},{"id":"W2054963091","doi":"10.1051/medsci/200824165","title":"Les dys-fonctionnements du transport axonal dans les neuropathies et motoneuronopathies","year":2008,"lang":"fr","type":"review","venue":"médecine/sciences","topic":"Hereditary Neurological Disorders","field":"Neuroscience","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":"Wilfrid Laurier University; Centre hospitalier de l'Université Laval","funders":"","keywords":"Medicine","score_opus":0.12852715444995222,"score_gpt":0.3276320218821538,"score_spread":0.19910486743220157,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2054963091","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":[0.00041471134,0.9967483,0.00031491317,0.00019106061,0.00015874459,0.000005430957,0.000015268988,0.000013139802,0.0021383332],"genre_scores_gemma":[0.0026285425,0.9947187,0.00035893288,0.00012887771,0.00012324084,0.000010240792,0.000029095034,0.0000021693563,0.0020002732],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.9998272,0.00003187014,0.000018968885,0.000039744133,0.000059994913,0.000022298816],"domain_scores_gemma":[0.99978,0.000095991665,0.00003377826,0.000010463856,0.000063392006,0.000016398011],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00050112006,0.0010330462,0.0012843638,0.0023614517,0.0004790042,0.001055663,0.0008290096,0.0016013079,0.0024544157],"category_scores_gemma":[0.0005273766,0.0002732117,0.0004181546,0.0023412725,0.000999706,0.0014197871,0.0005104576,0.0011334178,0.0017386465],"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":[0.000095272204,0.000069243295,0.00044779587,0.011644893,0.00008224939,0.00089437974,0.00017550703,0.00055704196,0.0075978567,0.007135168,0.015934275,0.9553663],"study_design_scores_gemma":[0.00002208023,0.00014136867,0.0029172574,0.002409799,0.00012792026,0.0066360235,0.0002013493,0.00017776115,0.0032687706,0.0039252755,0.98013866,0.00003370621],"about_ca_topic_score_codex":0.002969951,"about_ca_topic_score_gemma":0.0040283147,"teacher_disagreement_score":0.002969951,"about_ca_system_score_codex":0.0010569043,"about_ca_system_score_gemma":0.0011766332,"threshold_uncertainty_score":0.008210897},"labels":[],"label_agreement":null},{"id":"W2055197986","doi":"10.1002/ana.20239","title":"A novel locus for pure recessive hereditary spastic paraplegia maps to 10q22.1‐10q24.1","year":2004,"lang":"en","type":"article","venue":"Annals of Neurology","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":53,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"McGill University Health Centre","funders":"","keywords":"Locus (genetics); Genetics; Allele; Hereditary spastic paraplegia; Biology; Spasticity; Spastic; Degenerative disease; Genetic linkage; Gene; Medicine; Central nervous system disease; Neuroscience; Phenotype; Cerebral palsy","score_opus":0.10590668766363025,"score_gpt":0.3332684959480686,"score_spread":0.22736180828443836,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2055197986","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":[0.9900799,0.0014364193,0.0052187443,0.0001845415,0.000052852713,0.000033058015,0.0005646097,0.00018053515,0.002249308],"genre_scores_gemma":[0.98823804,0.0009417429,0.0064227693,0.00009987365,0.000041482097,0.000048946844,0.001478915,0.000021831029,0.0027063298],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.99989057,0.000015170701,0.000007055381,0.0000370629,0.000029268685,0.000020862044],"domain_scores_gemma":[0.9998443,0.000037423742,0.000050257968,0.000010301634,0.00001717659,0.000040504714],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0001445821,0.00082595414,0.0004387761,0.000665748,0.00025274348,0.00028948195,0.00045871633,0.00033890206,0.0023009344],"category_scores_gemma":[0.00028710745,0.00029283937,0.00021347599,0.0003505183,0.0002747623,0.00009452028,0.00045609436,0.00033519222,0.0005173886],"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":[0.0006807081,0.00018588807,0.041708592,0.00028150532,0.0002770136,0.030880472,0.00048696296,0.0005918849,0.8709726,0.002147356,0.0015362776,0.05025077],"study_design_scores_gemma":[0.0006194849,0.0016126483,0.6365603,0.00022980214,0.0007856471,0.18408348,0.0004398482,0.0025036912,0.13544057,0.003448285,0.034166723,0.00010951266],"about_ca_topic_score_codex":0.0010436906,"about_ca_topic_score_gemma":0.0029370915,"teacher_disagreement_score":0.0023009344,"about_ca_system_score_codex":0.0002886645,"about_ca_system_score_gemma":0.00034469774,"threshold_uncertainty_score":0.007697463},"labels":[],"label_agreement":null},{"id":"W2055343760","doi":"10.1002/glia.20766","title":"Interactions between Schwann cells and macrophages in injury and inherited demyelinating disease","year":2008,"lang":"en","type":"review","venue":"Glia","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":324,"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":"Canadian Institutes of Health Research","keywords":"Wallerian degeneration; Myelin; Biology; Schwann cell; Macrophage; Chemokine; Neuroscience; Demyelinating disease; Cell biology; Immunology; Inflammation; Central nervous system","score_opus":0.08709792702900146,"score_gpt":0.3562656817277825,"score_spread":0.26916775469878107,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2055343760","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":[0.00017286543,0.99818027,0.0001383889,0.00020428344,0.0002175482,0.0000026185821,0.0000048859956,0.0000069404214,0.0010722204],"genre_scores_gemma":[0.0011382053,0.9969079,0.00027300674,0.00016087732,0.00027292786,0.0000065024956,0.000014417093,0.0000013963979,0.0012247864],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.9998375,0.000034611334,0.000022994569,0.000025093692,0.00006461674,0.000015128332],"domain_scores_gemma":[0.9998265,0.00007309258,0.00002526195,0.000005772603,0.000042797266,0.000026588687],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00047059217,0.0010309279,0.0011588803,0.0018420236,0.00035338724,0.0008886941,0.0007750671,0.0014503739,0.0027023263],"category_scores_gemma":[0.00042241302,0.00020512792,0.00022067853,0.0019537776,0.000665532,0.0014818382,0.0006681879,0.0010216376,0.0023962157],"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":[0.00008311527,0.000065456785,0.00039049692,0.0066318125,0.000052551182,0.00097442156,0.00014945334,0.0003777214,0.0029332188,0.00531603,0.022080673,0.960945],"study_design_scores_gemma":[0.000014695476,0.0000922084,0.0019479209,0.0020594795,0.000045428114,0.005692092,0.00017370851,0.00006379389,0.00057392765,0.0035452207,0.985775,0.00001653606],"about_ca_topic_score_codex":0.00095908233,"about_ca_topic_score_gemma":0.0016841127,"teacher_disagreement_score":0.0027023263,"about_ca_system_score_codex":0.000701875,"about_ca_system_score_gemma":0.0007203086,"threshold_uncertainty_score":0.009040177},"labels":[],"label_agreement":null},{"id":"W2056843507","doi":"10.1007/s10897-013-9584-4","title":"A Review of Genetic Counseling for Charcot Marie Tooth Disease (CMT)","year":2013,"lang":"en","type":"review","venue":"Journal of Genetic Counseling","topic":"Hereditary Neurological Disorders","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":"University of Toronto; Mount Sinai Hospital","funders":"","keywords":"Genetic counseling; Psychosocial; Disease; Genetic testing; Genetics; Medicine; Human genetics; Population; Tooth disease; Gene; Biology; Pathology; Psychiatry; Environmental health","score_opus":0.08004496106333414,"score_gpt":0.33653523174302025,"score_spread":0.2564902706796861,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2056843507","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":[0.00014627376,0.9970783,0.00020632314,0.00043551036,0.0005074281,0.000007029381,0.000029015297,0.000015666887,0.0015744212],"genre_scores_gemma":[0.0007051789,0.9977325,0.0003728223,0.00028659112,0.00034127015,0.000007190931,0.00004604819,0.0000029388982,0.0005055211],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.9996393,0.00006798054,0.00007861176,0.00005974528,0.00013104391,0.00002323024],"domain_scores_gemma":[0.99918574,0.00043154423,0.000116243624,0.000016630254,0.0001842961,0.00006557245],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0005998725,0.0010238956,0.0012081681,0.004615634,0.00037209404,0.00075742137,0.0010078225,0.0010493221,0.0053355168],"category_scores_gemma":[0.0019052242,0.0002939039,0.00045790718,0.0043059066,0.00043068494,0.0012620697,0.0005184895,0.0011266125,0.0028015103],"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":[0.000027724527,0.00004559899,0.00031588133,0.01757121,0.00007726498,0.0011292615,0.00011164251,0.00022029455,0.00069682277,0.0016590451,0.107929066,0.8702162],"study_design_scores_gemma":[0.000015763168,0.00006412268,0.002226758,0.0140503375,0.00019356485,0.01797817,0.0001533223,0.00008580693,0.00024590018,0.0012808713,0.9636684,0.000036898346],"about_ca_topic_score_codex":0.0016715737,"about_ca_topic_score_gemma":0.0029501321,"teacher_disagreement_score":0.0053355168,"about_ca_system_score_codex":0.00065129524,"about_ca_system_score_gemma":0.0012790961,"threshold_uncertainty_score":0.017849088},"labels":[],"label_agreement":null},{"id":"W2057578597","doi":"10.1016/j.ejmg.2013.06.004","title":"Charcot–Marie–Tooth 1B caused by expansion of a familial myelin protein zero (MPZ) gene duplication","year":2013,"lang":"en","type":"article","venue":"European Journal of Medical Genetics","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":44,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Credit Valley Hospital; University of Toronto; Trillium Health Centre","funders":"","keywords":"Missense mutation; Gene duplication; Myelin; Genetics; Gene; Biology; Peripheral myelin protein 22; Mutation; Leukodystrophy; Medicine; Disease; Pathology; Central nervous system; Neuroscience","score_opus":0.02895978806509065,"score_gpt":0.25036706610869114,"score_spread":0.2214072780436005,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2057578597","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":[0.9920636,0.0007019581,0.0015893319,0.001076904,0.00017245143,0.000077214754,0.00022154818,0.000119204036,0.00397791],"genre_scores_gemma":[0.99717027,0.00016704855,0.0009821322,0.00024512643,0.000089182926,0.000016278726,0.00008165456,0.000027388698,0.0012209169],"study_design_codex":"case_report","study_design_gemma":"observational","domain_scores_codex":[0.9995759,0.00004681103,0.00004492243,0.00012226168,0.00010711289,0.00010291618],"domain_scores_gemma":[0.9990978,0.0003083954,0.00020088578,0.00004175445,0.000054185988,0.0002968826],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00024434298,0.0016892287,0.0008191859,0.0015028258,0.0016289908,0.00064559357,0.0011616572,0.0039360207,0.0020522869],"category_scores_gemma":[0.0017382394,0.00061318866,0.00096834806,0.00095656223,0.0016201299,0.00042655558,0.0010101993,0.0015461029,0.000713146],"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":[0.00014831978,0.000047230173,0.0023464253,0.000036850975,0.000020323965,0.978022,0.00013702459,0.00014137663,0.01748778,0.0003331116,0.0002429105,0.0010365846],"study_design_scores_gemma":[0.000110686815,0.00011791668,0.015499766,0.000024682782,0.000060462466,0.97532606,0.00012026221,0.0010986842,0.006096357,0.00046489917,0.0010425799,0.000037537884],"about_ca_topic_score_codex":0.004354,"about_ca_topic_score_gemma":0.0029794315,"teacher_disagreement_score":0.004354,"about_ca_system_score_codex":0.0011774489,"about_ca_system_score_gemma":0.00075933797,"threshold_uncertainty_score":0.008657336},"labels":[],"label_agreement":null},{"id":"W2058923226","doi":"10.1177/08830738030180011901","title":"Andermann Syndrome in a Turkish Patient","year":2003,"lang":"en","type":"article","venue":"Journal of Child Neurology","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":3,"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":"Agenesis of the corpus callosum; Medicine; Corpus Callosum Agenesis; Corpus callosum; Anatomy; Agenesis; Hereditary motor and sensory neuropathy; Pathology","score_opus":0.014382556889686296,"score_gpt":0.22582986995140708,"score_spread":0.2114473130617208,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2058923226","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":[0.997584,0.00035793564,0.00023880452,0.00016478007,0.000029267187,0.000018197348,0.00006905779,0.000032241038,0.0015057041],"genre_scores_gemma":[0.9986712,0.00019755383,0.0003274035,0.000105738305,0.000020466487,0.000008244978,0.00005982693,0.000008127919,0.0006014893],"study_design_codex":"case_report","study_design_gemma":"case_report","domain_scores_codex":[0.9997267,0.000028964221,0.000029675868,0.00007556464,0.000038479757,0.00010058605],"domain_scores_gemma":[0.9997229,0.000058145157,0.00009162229,0.00001654143,0.00002845123,0.00008230783],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00015906956,0.0014878709,0.0006221475,0.0007671231,0.0011638264,0.0005368735,0.00045351544,0.001225421,0.0014863437],"category_scores_gemma":[0.0011608984,0.00040307982,0.00039292607,0.0005295817,0.00052080763,0.00045964948,0.0005413128,0.0004692466,0.00030107299],"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":[0.00022727106,0.0000990788,0.03880836,0.00006193521,0.000042703006,0.93695796,0.0010072418,0.00015622137,0.015380416,0.00040821574,0.00066818617,0.006182406],"study_design_scores_gemma":[0.00005700024,0.0002529724,0.04681192,0.000024753295,0.00006847926,0.94892263,0.0005067412,0.00028845342,0.0016952103,0.0001692846,0.0011657462,0.000036787562],"about_ca_topic_score_codex":0.005448544,"about_ca_topic_score_gemma":0.005337939,"teacher_disagreement_score":0.005448544,"about_ca_system_score_codex":0.00061512645,"about_ca_system_score_gemma":0.0005885078,"threshold_uncertainty_score":0.010833681},"labels":[],"label_agreement":null},{"id":"W2059892947","doi":"10.1523/jneurosci.5168-04.2005","title":"Adherens Junctions in Myelinating Schwann Cells Stabilize Schmidt-Lanterman Incisures via Recruitment of p120 Catenin to E-Cadherin","year":2005,"lang":"en","type":"article","venue":"Journal of Neuroscience","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":79,"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; Hakai Institute; National Institutes of Health; Philippe Foundation","keywords":"Adherens junction; Cadherin; Cell biology; Catenin; Cytoplasm; Biology; Schwann cell; Actin cytoskeleton; Actin; Cytoskeleton; Biochemistry; Cell; Signal transduction; Wnt signaling pathway","score_opus":0.10852118813607947,"score_gpt":0.33438539599423606,"score_spread":0.22586420785815658,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2059892947","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":[0.9980501,0.00044827373,0.000696412,0.000020508742,0.000006795274,0.000005751931,0.000028903212,0.000024630213,0.0007187368],"genre_scores_gemma":[0.9965591,0.00030281028,0.0008071484,0.000017190649,0.0000031924542,0.000012164377,0.000121422796,0.0000059235667,0.002171082],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99988973,0.0000125328925,0.000010170191,0.000018267783,0.000035347224,0.000033866152],"domain_scores_gemma":[0.9999019,0.0000070753385,0.00002613803,0.000011456535,0.000014095596,0.000039417857],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00010373395,0.00021334962,0.00012044124,0.00017916442,0.00020427734,0.00026387582,0.00018752669,0.000266312,0.0008055515],"category_scores_gemma":[0.0001058883,0.00012728797,0.00021287292,0.00010701913,0.00015305483,0.00020215969,0.00024631692,0.0005381182,0.0003384331],"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":[0.00003442442,0.000009503732,0.000108689164,0.000011091763,0.0000021127892,0.000040420047,0.0000132959685,0.000019138472,0.99921227,0.00008050754,0.000007545869,0.00046103226],"study_design_scores_gemma":[0.000012369286,0.00018732177,0.009765787,0.0000061366864,0.000011912262,0.00023114856,0.00006580619,0.0008632445,0.987158,0.00008200529,0.0016121712,0.0000042134334],"about_ca_topic_score_codex":0.0007021109,"about_ca_topic_score_gemma":0.00096468127,"teacher_disagreement_score":0.0008055515,"about_ca_system_score_codex":0.00023650941,"about_ca_system_score_gemma":0.00018866968,"threshold_uncertainty_score":0.0026948452},"labels":[],"label_agreement":null},{"id":"W2061954667","doi":"10.1111/j.1750-3639.2004.tb00066.x","title":"A Pathogenic Peripherin Gene Mutation in a Patient with Amyotrophic Lateral Sclerosis","year":2004,"lang":"en","type":"article","venue":"Brain Pathology","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":114,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Columbia College","funders":"National Institute of Neurological Disorders and Stroke; National Institute on Aging","keywords":"Peripherin; Mutation; Neurofilament; Intermediate filament; Amyotrophic lateral sclerosis; Biology; Motor neuron; Mutant; Gene mutation; Cell biology; Genetics; Spinal cord; Gene; Pathology; Neuroscience; Medicine; Immunology; Cell; Disease; Cytoskeleton","score_opus":0.02411780715651658,"score_gpt":0.22320618110737273,"score_spread":0.19908837395085616,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2061954667","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":[0.996088,0.00040459263,0.0010166317,0.0004376179,0.000039499322,0.00004453132,0.00011077701,0.00006134999,0.0017969209],"genre_scores_gemma":[0.9982765,0.00014242431,0.0005413011,0.00015083516,0.000048509864,0.000008392907,0.000048589132,0.000009564108,0.0007738445],"study_design_codex":"case_report","study_design_gemma":"case_report","domain_scores_codex":[0.9998048,0.000023875196,0.00002216255,0.00007036007,0.00004471859,0.000034091106],"domain_scores_gemma":[0.9996284,0.000117059346,0.0000597505,0.00001744278,0.000030209962,0.00014711545],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00022319451,0.00097909,0.00054080255,0.00084911863,0.0011178539,0.00032923493,0.00034194448,0.0017265724,0.0016513955],"category_scores_gemma":[0.0011201771,0.00038362356,0.0002954057,0.00035034874,0.0007360216,0.000455028,0.0005599614,0.0007364822,0.00038773162],"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":[0.00028804634,0.0001339909,0.015606509,0.000068261565,0.00004268531,0.92362845,0.000870452,0.00026197344,0.052758645,0.00036170235,0.0005065165,0.005472692],"study_design_scores_gemma":[0.00007891697,0.00069138926,0.04287652,0.000022628343,0.00006927998,0.94600016,0.00018045955,0.00076201075,0.007586209,0.00045329664,0.0012327904,0.000046375913],"about_ca_topic_score_codex":0.000747761,"about_ca_topic_score_gemma":0.00110405,"teacher_disagreement_score":0.0017265724,"about_ca_system_score_codex":0.00033280885,"about_ca_system_score_gemma":0.00030562037,"threshold_uncertainty_score":0.005524516},"labels":[],"label_agreement":null},{"id":"W2062911196","doi":"10.1212/wnl.0000000000000206","title":"Ubiquitin ligase defect by <i>DCAF8</i> mutation causes HMSN2 with giant axons","year":2014,"lang":"en","type":"article","venue":"Neurology","topic":"Hereditary Neurological Disorders","field":"Neuroscience","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 Cancer Institute; National Institute of Neurological Disorders and Stroke; University of Toronto","keywords":"Ubiquitin ligase; Biology; Mutation; Genetics; Exome sequencing; Ubiquitin; Sanger sequencing; Haplotype; Molecular biology; Gene; Allele","score_opus":0.01488663744165143,"score_gpt":0.2289282393802159,"score_spread":0.21404160193856447,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2062911196","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":[0.9988954,0.00009373145,0.0004169848,0.000050352544,0.0000043625823,0.0000105934305,0.000111693145,0.000017285543,0.00039953805],"genre_scores_gemma":[0.99872655,0.000060679828,0.0006307039,0.000043178108,0.000015907897,0.000008016253,0.0001735302,0.0000067795154,0.0003345769],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9998987,0.000010891262,0.000011417167,0.000040630217,0.00002184278,0.000016480813],"domain_scores_gemma":[0.9998604,0.000027618782,0.000054043656,0.0000070487727,0.000013890828,0.000036916343],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.000105667605,0.0007570108,0.00021201612,0.00029623462,0.00034399916,0.00014847702,0.00019816057,0.00047923098,0.001483185],"category_scores_gemma":[0.00027557663,0.000108011445,0.00022142442,0.00020553537,0.00026599507,0.00011294785,0.00022322664,0.00023882321,0.00023983087],"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":[0.0007349483,0.00025521728,0.28683844,0.00018907337,0.00019801743,0.2068921,0.000625885,0.0005355625,0.48939008,0.00031184568,0.0012718828,0.012756984],"study_design_scores_gemma":[0.000117515585,0.0006357553,0.51788616,0.00006539468,0.00019709213,0.4006438,0.0003308721,0.0023138053,0.074746974,0.00026434968,0.002772622,0.000025769488],"about_ca_topic_score_codex":0.0010801419,"about_ca_topic_score_gemma":0.0016004789,"teacher_disagreement_score":0.001483185,"about_ca_system_score_codex":0.00021011417,"about_ca_system_score_gemma":0.00012635127,"threshold_uncertainty_score":0.004961729},"labels":[],"label_agreement":null},{"id":"W2064225376","doi":"10.1136/jnnp-2014-308625","title":"Hereditary spastic paraplegia: a novel mutation and expansion of the phenotype variability in SPG10: Table 1","year":2014,"lang":"en","type":"letter","venue":"Journal of Neurology Neurosurgery & Psychiatry","topic":"Hereditary Neurological Disorders","field":"Neuroscience","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":"Canada Excellence Research Chairs, Government of Canada","keywords":"Hereditary spastic paraplegia; Biology; Genetic heterogeneity; Spasticity; Movement disorders; Genetics; Phenotype; Neuroscience; Gene; Medicine; Pathology; Physical medicine and rehabilitation; Disease","score_opus":0.023475250425103532,"score_gpt":0.23923101900926358,"score_spread":0.21575576858416004,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2064225376","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":[0.74130344,0.0059922524,0.0040892772,0.10676995,0.005381298,0.00033251595,0.012218473,0.0008191661,0.12309368],"genre_scores_gemma":[0.95592284,0.0022289378,0.0027126763,0.010580575,0.0032840858,0.00008637598,0.0022411526,0.00010546001,0.022837948],"study_design_codex":"case_report","study_design_gemma":"case_report","domain_scores_codex":[0.9997254,0.000029786948,0.00004274563,0.00008291365,0.000060083217,0.000059076734],"domain_scores_gemma":[0.9995554,0.00017437756,0.000065908425,0.000013979749,0.00007270615,0.00011764818],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00013953265,0.0009882009,0.00065901387,0.0011947334,0.00060140475,0.00066857017,0.000690177,0.004338883,0.011416062],"category_scores_gemma":[0.0011652607,0.00014253185,0.0004509348,0.0009419889,0.0004543326,0.0006714566,0.0003459352,0.0011742925,0.0027948166],"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":[0.00019179643,0.00008109694,0.020196076,0.00012237662,0.00002807571,0.9102138,0.00020854917,0.00031940706,0.009150816,0.0012837154,0.044533167,0.013671179],"study_design_scores_gemma":[0.000057948146,0.0001326383,0.0407729,0.00013967934,0.000044386343,0.92846996,0.00027835037,0.0011435451,0.0031536573,0.0023477506,0.02341431,0.00004486542],"about_ca_topic_score_codex":0.0026605825,"about_ca_topic_score_gemma":0.0020648933,"teacher_disagreement_score":0.011416062,"about_ca_system_score_codex":0.0006970722,"about_ca_system_score_gemma":0.000510069,"threshold_uncertainty_score":0.038190484},"labels":[],"label_agreement":null},{"id":"W2066939817","doi":"10.1074/jbc.m610314200","title":"NIPA1(SPG6), the Basis for Autosomal Dominant Form of Hereditary Spastic Paraplegia, Encodes a Functional Mg2+ Transporter","year":2006,"lang":"en","type":"article","venue":"Journal of Biological Chemistry","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":141,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of British Columbia","funders":"","keywords":"Hereditary spastic paraplegia; Endosome; Cell biology; Mutant; Biology; Transfection; Gene; Chemistry; Molecular biology; Phenotype; Biochemistry; Intracellular","score_opus":0.03633604833662743,"score_gpt":0.24042631449474228,"score_spread":0.20409026615811485,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2066939817","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":[0.9745,0.0045812544,0.011248545,0.0009703668,0.00021356155,0.00011650506,0.0028625852,0.0009263665,0.004580894],"genre_scores_gemma":[0.9812584,0.0025695201,0.0065211914,0.0002172259,0.0000579597,0.00007937534,0.0034170945,0.00006998091,0.0058093397],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99989164,0.000013928631,0.000010382179,0.00003022339,0.000043769884,0.000010106493],"domain_scores_gemma":[0.9998511,0.000021986862,0.00006084011,0.000008722896,0.000011317522,0.000046108536],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00011371773,0.0014828044,0.0003551216,0.00050343346,0.0002670598,0.00021457612,0.00059617567,0.0006369872,0.0028555754],"category_scores_gemma":[0.00024494945,0.00016281712,0.00035192224,0.0003301584,0.00045493955,0.00016320369,0.00054024457,0.0007134842,0.0013453248],"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":[0.0002062047,0.0000646379,0.0042503327,0.00023763232,0.00005557758,0.011425449,0.000060154296,0.00031096902,0.95979935,0.0009096079,0.0009701822,0.021709887],"study_design_scores_gemma":[0.00026339258,0.0010432968,0.14647207,0.00023618601,0.00025895913,0.235134,0.00019267162,0.0086969845,0.53514266,0.0027293896,0.06975459,0.00007581252],"about_ca_topic_score_codex":0.00037639163,"about_ca_topic_score_gemma":0.0003821742,"teacher_disagreement_score":0.0028555754,"about_ca_system_score_codex":0.00027227713,"about_ca_system_score_gemma":0.00030960856,"threshold_uncertainty_score":0.009552836},"labels":[],"label_agreement":null},{"id":"W2068086292","doi":"10.1007/s00415-011-6206-7","title":"Letter to the editors: comment on “Hereditary sensory and autonomic neuropathy II due to novel mutation in the HSN2 gene in Mexican families”","year":2011,"lang":"en","type":"letter","venue":"Journal of Neurology","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":1,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Centre Hospitalier Universitaire Sainte-Justine; Université de Montréal; Centre Hospitalier de l’Université de Montréal","funders":"","keywords":"Neuroradiology; Neurology; Sensory neuropathy; Mutation; Sensory system; Neuroscience; Autonomic neuropathy; Gene; Genetics; Medicine; Psychology; Biology; Internal medicine","score_opus":0.04035716280633015,"score_gpt":0.25007028124189845,"score_spread":0.2097131184355683,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2068086292","genre_codex":"commentary","genre_gemma":"commentary","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"commentary","genre_consensus":"commentary","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.0017421442,0.0009827949,0.000108632965,0.94794846,0.04711159,0.000018418856,0.00009544223,0.00005364235,0.0019388373],"genre_scores_gemma":[0.016474795,0.0011064643,0.00023678002,0.89168787,0.08520766,0.000050518196,0.00007650072,0.000046836794,0.0051126],"study_design_codex":"not_applicable","study_design_gemma":"not_applicable","domain_scores_codex":[0.99830484,0.00042838042,0.00024956698,0.0003289864,0.00033016,0.00035806792],"domain_scores_gemma":[0.99588096,0.0021078002,0.00047302755,0.00014697418,0.00077743776,0.0006137653],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0018834252,0.0009864884,0.0016572018,0.00079365197,0.0025581818,0.002288894,0.0021332835,0.03774457,0.0040357234],"category_scores_gemma":[0.018344952,0.00088273,0.0012772518,0.00071706594,0.0018770216,0.0023540033,0.0009874866,0.022805452,0.0040328857],"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":[0.0001547478,0.00004843254,0.0014298103,0.00008033786,0.000038917155,0.014447123,0.00017469359,0.000086389344,0.0002586257,0.0008397621,0.97886276,0.0035784498],"study_design_scores_gemma":[0.0005857577,0.00031843025,0.009742869,0.0006557038,0.00025470604,0.03645993,0.0016118011,0.0020056798,0.0013835805,0.008147678,0.9385031,0.00033076853],"about_ca_topic_score_codex":0.003238733,"about_ca_topic_score_gemma":0.0036513,"teacher_disagreement_score":0.03774457,"about_ca_system_score_codex":0.0028014784,"about_ca_system_score_gemma":0.002029877,"threshold_uncertainty_score":0.020326257},"labels":[],"label_agreement":null},{"id":"W2076474126","doi":"10.1086/420795","title":"Identification of a Novel Gene (HSN2) Causing Hereditary Sensory and Autonomic Neuropathy Type II through the Study of Canadian Genetic Isolates","year":2004,"lang":"en","type":"article","venue":"The American Journal of Human Genetics","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":157,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":true,"ca_institutions":"McGill University Health Centre; University of British Columbia; McGill University; Centre Hospitalier de l’Université de Montréal; Memorial University of Newfoundland; Xenon Pharmaceuticals (Canada)","funders":"National Institute of Neurological Disorders and Stroke","keywords":"Identification (biology); Sensory neuropathy; Genetics; Gene; Autonomic neuropathy; Sensory system; Biology; Medicine; Neuroscience; Internal medicine","score_opus":0.049989384102248215,"score_gpt":0.2784099229621219,"score_spread":0.2284205388598737,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2076474126","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":[0.987818,0.00045045992,0.0013609704,0.0003509397,0.000062414,0.00008238946,0.0012442805,0.000018481927,0.008612064],"genre_scores_gemma":[0.9914466,0.0005619249,0.0022519608,0.00019916096,0.000018876954,0.000019146264,0.0009500279,0.000017123004,0.004535123],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9995214,0.000025740894,0.000018914281,0.00008898204,0.0001954677,0.00014959196],"domain_scores_gemma":[0.9995123,0.000058675632,0.000035964218,0.000018661121,0.00023898746,0.00013539348],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0002985906,0.0006881321,0.0004159902,0.0018098346,0.0030385978,0.00076181744,0.00060305087,0.0005537273,0.0018843199],"category_scores_gemma":[0.00094408006,0.00026809634,0.000452023,0.0020952427,0.0007317359,0.00015757352,0.0007624726,0.00066352374,0.0001897375],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":true,"about_ca_topic_consensus":true,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0024616057,0.00042934294,0.36568293,0.00033609068,0.00030362685,0.076809466,0.013380452,0.0023209685,0.46312258,0.007922717,0.007196223,0.060034074],"study_design_scores_gemma":[0.00019903529,0.00049975544,0.84794277,0.00011413198,0.00031642526,0.04740859,0.0065225665,0.0019179767,0.037333794,0.0006300215,0.056958806,0.00015613135],"about_ca_topic_score_codex":0.82808787,"about_ca_topic_score_gemma":0.85700524,"teacher_disagreement_score":0.17191213,"about_ca_system_score_codex":0.004665986,"about_ca_system_score_gemma":0.007177062,"threshold_uncertainty_score":0.3458491},"labels":[],"label_agreement":null},{"id":"W2078439332","doi":"10.1016/j.pediatrneurol.2007.11.005","title":"Congenital Axonal Neuropathy and Encephalopathy","year":2008,"lang":"en","type":"article","venue":"Pediatric Neurology","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":8,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Hôpital Charles-Le Moyne; Université de Montréal; Centre Hospitalier Universitaire Sainte-Justine","funders":"","keywords":"Medicine; Hypotonia; Pathology; Encephalopathy; Atrophy; Sural nerve; Ataxia; Pediatrics; Internal medicine","score_opus":0.03272043841525372,"score_gpt":0.22145341357492787,"score_spread":0.18873297515967416,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2078439332","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":[0.76293314,0.013067894,0.0017898551,0.0055224723,0.00073273183,0.00005938663,0.0005299508,0.000268067,0.21509644],"genre_scores_gemma":[0.97406244,0.0037042296,0.001033714,0.0007977683,0.0009126053,0.000015948483,0.0001798096,0.000039135302,0.019254334],"study_design_codex":"case_report","study_design_gemma":"observational","domain_scores_codex":[0.999762,0.00002906788,0.0000265889,0.000040225805,0.00004482329,0.00009727123],"domain_scores_gemma":[0.9993704,0.00026176198,0.0001263697,0.00004739361,0.000058385212,0.00013566739],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00023706387,0.0007523474,0.00045121,0.0017096561,0.001313827,0.0008859269,0.0005930476,0.0018206814,0.011503529],"category_scores_gemma":[0.0011624437,0.00030363328,0.00027239212,0.001206149,0.0015026347,0.0011603091,0.0010040164,0.0012734575,0.001119333],"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":[0.00013678058,0.00006601018,0.02091289,0.000113418224,0.00003490518,0.9524469,0.00020528262,0.00019323047,0.0014676772,0.008135847,0.0036946873,0.012592505],"study_design_scores_gemma":[0.000022100836,0.00006179888,0.024790198,0.000042065916,0.000041052725,0.96526426,0.00019400193,0.00021234037,0.0010759311,0.0031849993,0.005099164,0.000012069627],"about_ca_topic_score_codex":0.0033635534,"about_ca_topic_score_gemma":0.0055668196,"teacher_disagreement_score":0.011503529,"about_ca_system_score_codex":0.00083738356,"about_ca_system_score_gemma":0.0008655718,"threshold_uncertainty_score":0.038483083},"labels":[],"label_agreement":null},{"id":"W2079699073","doi":"10.1523/jneurosci.2834-12.2012","title":"<i>Drosophila</i>Vap-33 Is Required for Axonal Localization of Dscam Isoforms","year":2012,"lang":"en","type":"article","venue":"Journal of Neuroscience","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":21,"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":"Canadian Institutes of Health Research; ALS Association","keywords":"Biology; Gene isoform; Axon guidance; Phenotype; Transmembrane protein; Cell biology; Alternative splicing; Axon; Genetics; Neuroscience; Receptor; Gene","score_opus":0.07547986416578673,"score_gpt":0.3052381068748705,"score_spread":0.2297582427090838,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2079699073","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":[0.99502015,0.0004212322,0.0023041416,0.00007578901,0.000016058362,0.0000112254575,0.0006058026,0.00014591782,0.0013996119],"genre_scores_gemma":[0.9963768,0.00015631107,0.0012431764,0.000031285777,0.0000035808496,0.000010635784,0.0007473587,0.00006856949,0.0013622796],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9998646,0.000018439976,0.00001466402,0.000026161517,0.0000482287,0.000027908958],"domain_scores_gemma":[0.9997373,0.00004264133,0.0001005592,0.000021080023,0.000020518743,0.00007784995],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00007397769,0.00047953185,0.00018158909,0.0002679747,0.00025360886,0.00032981392,0.00027504904,0.00023303629,0.0018082226],"category_scores_gemma":[0.00014552206,0.0002268099,0.00019170948,0.00012379812,0.00026290675,0.00015746253,0.00041759695,0.00047594844,0.00099374],"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":[0.000021532655,0.000004499651,0.00019062737,0.000009612978,0.0000021702601,0.00010815426,0.000005661519,0.000039319348,0.99920624,0.00006688606,0.000027547987,0.00031782425],"study_design_scores_gemma":[0.000022259455,0.0000794087,0.02851861,0.00001597129,0.000016606835,0.0017740111,0.00006291019,0.0030303998,0.9623697,0.00011447389,0.0039814026,0.000014215881],"about_ca_topic_score_codex":0.002082502,"about_ca_topic_score_gemma":0.003570967,"teacher_disagreement_score":0.002082502,"about_ca_system_score_codex":0.00043475957,"about_ca_system_score_gemma":0.00022524188,"threshold_uncertainty_score":0.0060490966},"labels":[],"label_agreement":null},{"id":"W2080360508","doi":"10.1097/nen.0b013e3181a5deeb","title":"Mitochondrial and Axonal Abnormalities Precede Disruption of the Neurofilament Network in a Model of Charcot-Marie-Tooth Disease Type 2E and Are Prevented by Heat Shock Proteins in a Mutant-Specific Fashion","year":2009,"lang":"en","type":"article","venue":"Journal of Neuropathology & Experimental Neurology","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":53,"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; Montreal Neurological Institute and Hospital","funders":"McGill University","keywords":"Neurofilament; Biology; Cell biology; Motor neuron; Heat shock protein; Protein subunit; Mutant; Neurodegeneration; Mitochondrion; Neuroscience; Spinal cord; Genetics; Gene; Pathology; Immunology; Medicine; Disease","score_opus":0.023583649828560878,"score_gpt":0.2549331611536325,"score_spread":0.23134951132507164,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2080360508","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":[0.99781895,0.00056449743,0.00050682604,0.000065104585,0.000023680886,0.000033239994,0.00013843317,0.000053233845,0.00079602684],"genre_scores_gemma":[0.99564904,0.00047443138,0.0008196435,0.00003851332,0.000008551928,0.00006415628,0.00031540816,0.000012195821,0.002618102],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9998568,0.000023055882,0.000014759789,0.000038330887,0.000033279084,0.000033745084],"domain_scores_gemma":[0.9998011,0.000019726302,0.000057578614,0.000017840477,0.000013764376,0.00009006043],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0001451046,0.00049812143,0.00024757633,0.0004204317,0.00024637635,0.00024755482,0.00021105606,0.00047747002,0.0010605737],"category_scores_gemma":[0.00016699573,0.00027538778,0.00024773995,0.0001691462,0.00030707047,0.00024126109,0.00023080384,0.00073018664,0.00024680045],"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":[0.0006006708,0.00012338313,0.00052814337,0.000040646053,0.000010614863,0.00042870137,0.000028831413,0.0000872056,0.99737453,0.00010326473,0.000051588875,0.000622459],"study_design_scores_gemma":[0.00020560143,0.004278626,0.051445123,0.000043507378,0.000078587706,0.00590273,0.0001451101,0.002943681,0.9285347,0.00029652638,0.006097085,0.000028844292],"about_ca_topic_score_codex":0.0011812476,"about_ca_topic_score_gemma":0.0024519945,"teacher_disagreement_score":0.0011812476,"about_ca_system_score_codex":0.00054034445,"about_ca_system_score_gemma":0.000207986,"threshold_uncertainty_score":0.0039204955},"labels":[],"label_agreement":null},{"id":"W2081517843","doi":"10.1038/sc.2011.193","title":"Bladder dysfunction in hereditary spastic paraplegia: a clinical and urodynamic evaluation","year":2012,"lang":"en","type":"article","venue":"Spinal Cord","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":24,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Canadian Nautical Research Society","funders":"Hospices Civils de Lyon","keywords":"Medicine; Dyssynergia; Nocturia; Overactive bladder; Urinary system; Spinal cord injury; Hereditary spastic paraplegia; Urology; Urinary incontinence; Paraplegia; Detrusor sphincter dyssynergia; Etiology; Lower urinary tract symptoms; Neurological disorder; Spasticity; Internal medicine; Central nervous system disease; Spinal cord; Anesthesia; Pathology; Prostate","score_opus":0.1467783688034127,"score_gpt":0.38941374223001574,"score_spread":0.24263537342660305,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2081517843","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":[0.99494356,0.0012758189,0.00021884612,0.00016480222,0.00001650552,0.000050991595,0.00018716062,0.000013923134,0.0031283644],"genre_scores_gemma":[0.99877304,0.0003765959,0.00016386114,0.0001230018,0.000043048916,0.000017777182,0.00015938304,0.0000039347883,0.00033930046],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9996319,0.00008078767,0.00006132747,0.000057789228,0.0000786495,0.00008951168],"domain_scores_gemma":[0.9988859,0.0003520782,0.0001032459,0.00003118406,0.00015954554,0.00046801142],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0005379274,0.0009178878,0.0009510996,0.0021241019,0.00083317637,0.00037593982,0.00051038974,0.0011213783,0.00176979],"category_scores_gemma":[0.0027769026,0.0003759819,0.00045579358,0.00097063155,0.0013163422,0.000818761,0.0006337297,0.00052907865,0.00021407606],"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":[0.0014406135,0.0007176642,0.8030996,0.00016694285,0.000083865714,0.17355677,0.0008802566,0.0004334965,0.008351119,0.00022420504,0.00062525796,0.010420206],"study_design_scores_gemma":[0.00004867954,0.0017079271,0.83859783,0.000038650265,0.00008523846,0.15659095,0.0006257892,0.0005787941,0.0010620429,0.000133529,0.00049926207,0.000031335985],"about_ca_topic_score_codex":0.004232365,"about_ca_topic_score_gemma":0.0035884378,"teacher_disagreement_score":0.004232365,"about_ca_system_score_codex":0.000556642,"about_ca_system_score_gemma":0.0007689939,"threshold_uncertainty_score":0.008415461},"labels":[],"label_agreement":null},{"id":"W2084364398","doi":"10.1016/j.jns.2013.07.1860","title":"Genetics and underlying mechanisms associated with hereditary sensory and autonomic neuropathies","year":2013,"lang":"en","type":"article","venue":"Journal of the Neurological Sciences","topic":"Hereditary Neurological Disorders","field":"Neuroscience","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":"McGill University; Montreal Neurological Institute and Hospital","funders":"","keywords":"Exon; Exome sequencing; Genetics; Exome; Biology; Mutation; Gene; Genetic heterogeneity; Phenotype","score_opus":0.06427341463012397,"score_gpt":0.2553267575358162,"score_spread":0.1910533429056922,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2084364398","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":[0.9907799,0.0026424963,0.0010517291,0.00048822054,0.000044698078,0.000014648801,0.00012797318,0.00004694855,0.004803544],"genre_scores_gemma":[0.99758995,0.00095392653,0.00059749815,0.00008294132,0.00008633354,0.0000064794626,0.000073431635,0.000012112597,0.0005973292],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99962795,0.00009015747,0.000050555383,0.0000903433,0.000078506884,0.00006242418],"domain_scores_gemma":[0.99945873,0.00020718387,0.00019366991,0.000026285694,0.00003524103,0.000078829],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00030661793,0.0011364163,0.00046276013,0.0021257843,0.0006837056,0.0006565352,0.0007381306,0.0012208016,0.0035324923],"category_scores_gemma":[0.001177432,0.0002859328,0.00038006002,0.0011953469,0.0015042982,0.00070521736,0.00059629383,0.0005466997,0.00023245266],"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":[0.0020706044,0.0006664356,0.4257449,0.00029620124,0.0007186767,0.39036867,0.0015863092,0.0025434487,0.12371294,0.02497815,0.0013788773,0.02593477],"study_design_scores_gemma":[0.00026911602,0.0005249317,0.51677036,0.00026999338,0.0011516265,0.43816903,0.0019637335,0.003797043,0.016714308,0.016892228,0.0033579678,0.00011966714],"about_ca_topic_score_codex":0.0011282638,"about_ca_topic_score_gemma":0.000920575,"teacher_disagreement_score":0.0035324923,"about_ca_system_score_codex":0.00035193097,"about_ca_system_score_gemma":0.0004219856,"threshold_uncertainty_score":0.011817396},"labels":[],"label_agreement":null},{"id":"W2084603854","doi":"10.1097/cnd.0b013e318209efc6","title":"Hereditary Spastic Paraplegia Associated With Axonal Neuropathy: A Novel Mutation of SPG3A in a Large Family","year":2011,"lang":"en","type":"article","venue":"Journal of Clinical Neuromuscular Disease","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":12,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"SickKids Foundation; Hospital for Sick Children; University of Toronto","funders":"","keywords":"Hereditary spastic paraplegia; Paraplegia; Medicine; Spastic; Mutation; Population; Pediatrics; Physical medicine and rehabilitation; Gene; Genetics; Phenotype; Cerebral palsy; Spinal cord; Psychiatry; Biology","score_opus":0.1240041816746564,"score_gpt":0.3243244783887795,"score_spread":0.20032029671412308,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2084603854","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":[0.99242264,0.00059679203,0.0026017083,0.00062534347,0.00010180928,0.00009151696,0.00041967805,0.00015076945,0.0029897012],"genre_scores_gemma":[0.9968315,0.00023749763,0.0011987722,0.00019900808,0.00011164471,0.000036870908,0.00015974013,0.000034377364,0.0011905656],"study_design_codex":"case_report","study_design_gemma":"observational","domain_scores_codex":[0.99958163,0.00006198179,0.000034772773,0.00014217895,0.0001223711,0.000057031288],"domain_scores_gemma":[0.9992101,0.00026521398,0.000120402496,0.00003424991,0.00008824777,0.00028165968],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00038042996,0.0028314672,0.0009068694,0.0016695173,0.0021755446,0.00051276595,0.00076905946,0.0015968409,0.00395059],"category_scores_gemma":[0.0017721739,0.0005808455,0.00086669426,0.0011101849,0.0012649249,0.00046071527,0.0011013881,0.0010478791,0.0007217464],"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":[0.0003069061,0.00026427433,0.03740469,0.00011007656,0.00019864787,0.9140746,0.0020011284,0.00038307387,0.03096858,0.000804897,0.002142731,0.011340334],"study_design_scores_gemma":[0.00008903744,0.00034042436,0.07522115,0.000075108794,0.0002051492,0.9136528,0.00037871997,0.0012159355,0.005168899,0.0006772329,0.0028877254,0.000087705375],"about_ca_topic_score_codex":0.0053347275,"about_ca_topic_score_gemma":0.0052154404,"teacher_disagreement_score":0.0053347275,"about_ca_system_score_codex":0.00065783696,"about_ca_system_score_gemma":0.0008117615,"threshold_uncertainty_score":0.013216078},"labels":[],"label_agreement":null},{"id":"W2084685622","doi":"10.14740/jmc.v5i7.1806","title":"Recurrent Thromboembolic Events in a Patient With Dysautonomia: A Case Report","year":2014,"lang":"en","type":"article","venue":"Journal of Medical Cases","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":1,"is_retracted":false,"has_abstract":true,"route_ca_aff":false,"route_ca_fund":false,"route_ca_venue":true,"route_about_ca":false,"ca_institutions":"","funders":"","keywords":"Medicine; Dysautonomia; Etiology; Amaurosis fugax; Paradoxical embolism; Pediatrics; Cardiology; Internal medicine; Surgery; Migraine; Disease; Carotid arteries; Patent foramen ovale","score_opus":0.03809638230825848,"score_gpt":0.30291987849927793,"score_spread":0.26482349619101947,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2084685622","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":[0.97041106,0.011238048,0.003317555,0.0034485997,0.00054862763,0.00018313497,0.00027911464,0.00022806277,0.010345696],"genre_scores_gemma":[0.9912102,0.0038190633,0.0012748891,0.0008137745,0.0012961079,0.00003404738,0.00014124041,0.000029053665,0.001381547],"study_design_codex":"case_report","study_design_gemma":"case_report","domain_scores_codex":[0.9992423,0.00009730035,0.00012059392,0.00019661734,0.00012738824,0.00021588014],"domain_scores_gemma":[0.9985207,0.00038631237,0.00040814045,0.00011639713,0.00009695452,0.00047141968],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00042199343,0.0018966014,0.0013805125,0.003303634,0.002746828,0.0023910087,0.0010877075,0.004560729,0.0025339879],"category_scores_gemma":[0.0032032705,0.0012298679,0.0010484029,0.0018186702,0.0014237678,0.0023419778,0.0017874271,0.0028044186,0.0010920491],"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":[0.00001086699,0.0000320917,0.0056003253,0.000014420153,0.0000071165655,0.99307114,0.0001615468,0.00002176442,0.0002072647,0.00006082569,0.00018910907,0.0006236018],"study_design_scores_gemma":[0.000002972823,0.000017516148,0.0013602992,0.0000054635525,0.000006190367,0.9982139,0.000065985885,0.000044673114,0.000055841447,0.000042105257,0.00018073987,0.0000044200747],"about_ca_topic_score_codex":0.0017020878,"about_ca_topic_score_gemma":0.0017226081,"teacher_disagreement_score":0.004560729,"about_ca_system_score_codex":0.0008816503,"about_ca_system_score_gemma":0.0007085436,"threshold_uncertainty_score":0.008477092},"labels":[],"label_agreement":null},{"id":"W2087816368","doi":"10.1002/mds.20775","title":"Clinical and genetic study of a Brazilian family with spastic paraplegia (<i>SPG6 locus</i>)","year":2005,"lang":"en","type":"article","venue":"Movement Disorders","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":23,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Toronto Western Hospital; Occupational Cancer Research Centre; University of Toronto","funders":"","keywords":"Hereditary spastic paraplegia; Paraplegia; Spastic; Medicine; Physical medicine and rehabilitation; Family history; Locus (genetics); Gait Disturbance; Genetics; Physical therapy; Gene; Biology; Psychiatry; Internal medicine; Cerebral palsy; Phenotype; Spinal cord","score_opus":0.025257908664626415,"score_gpt":0.28034891453389255,"score_spread":0.25509100586926614,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2087816368","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":[0.9949597,0.00048336247,0.00076589186,0.0002976977,0.000015813659,0.000057603334,0.00019859234,0.00002147112,0.0031998728],"genre_scores_gemma":[0.9978276,0.00059411325,0.00066143373,0.00015506828,0.00001776874,0.000017030487,0.00018495192,0.000010680879,0.0005314726],"study_design_codex":"case_report","study_design_gemma":"observational","domain_scores_codex":[0.99975675,0.000054374897,0.000025859192,0.00007357036,0.00004920418,0.000040252264],"domain_scores_gemma":[0.99958986,0.000109225366,0.00007103337,0.00003092258,0.000064325264,0.00013460754],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00032211267,0.0013914236,0.0005057626,0.0012021322,0.0012906761,0.00035243173,0.00043496105,0.00080281805,0.0015758871],"category_scores_gemma":[0.0019036923,0.00039765507,0.0003846773,0.0005612749,0.0008563081,0.00021472285,0.00076003297,0.0005191052,0.00028652445],"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":[0.00022965953,0.0004557203,0.25309926,0.000118681055,0.00011114573,0.69254065,0.004253774,0.00026787218,0.032807156,0.0004778525,0.0007708538,0.014867384],"study_design_scores_gemma":[0.000051475152,0.00045240912,0.14450459,0.00004573128,0.00010224792,0.84895235,0.00074377516,0.00042394004,0.002068844,0.00027219244,0.002350535,0.000031887455],"about_ca_topic_score_codex":0.012196798,"about_ca_topic_score_gemma":0.007041276,"teacher_disagreement_score":0.012196798,"about_ca_system_score_codex":0.00048791993,"about_ca_system_score_gemma":0.00045112998,"threshold_uncertainty_score":0.02425164},"labels":[],"label_agreement":null},{"id":"W2087838338","doi":"10.1016/j.ajhg.2011.06.013","title":"KIF1A, an Axonal Transporter of Synaptic Vesicles, Is Mutated in Hereditary Sensory and Autonomic Neuropathy Type 2","year":2011,"lang":"en","type":"article","venue":"The American Journal of Human Genetics","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":205,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Centre Hospitalier Universitaire Sainte-Justine; Université de Montréal; Centre Hospitalier de l’Université de Montréal; NeuroRx Research (Canada)","funders":"Canadian Institutes of Health Research","keywords":"Genetics; Biology; Disease gene identification; Exon; Exome sequencing; Genetic heterogeneity; Mutation; Phenotype; Gene","score_opus":0.0595613303502034,"score_gpt":0.2650856132514359,"score_spread":0.20552428290123254,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2087838338","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":[0.99584097,0.00079617096,0.0010896656,0.00020924072,0.000094579875,0.000019385063,0.00027241718,0.00009454362,0.0015829356],"genre_scores_gemma":[0.9985512,0.00016072014,0.00046236644,0.000055043394,0.000033077937,0.0000059320237,0.00008604313,0.000019049246,0.000626629],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9997279,0.000033190936,0.000042096108,0.000069525384,0.00008807837,0.00003924163],"domain_scores_gemma":[0.9996147,0.0001203027,0.00012647596,0.000012016871,0.000035717145,0.000090788206],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00020555222,0.0012229227,0.0005945273,0.0013641593,0.00086850347,0.0004206598,0.0006559704,0.001464866,0.0026655837],"category_scores_gemma":[0.0010140719,0.00025818753,0.0004906997,0.0007130169,0.0006514535,0.00037728457,0.00046634793,0.00049009343,0.00038988734],"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":[0.0025030437,0.00039102358,0.09368251,0.00042072003,0.0006615009,0.43037456,0.0013799891,0.0019640706,0.43990728,0.0018485555,0.0026035877,0.024263028],"study_design_scores_gemma":[0.0002750023,0.00060998515,0.35785767,0.00020633385,0.0011619037,0.53497326,0.00096523785,0.009629559,0.084226064,0.0022220646,0.0077109644,0.00016190571],"about_ca_topic_score_codex":0.003943112,"about_ca_topic_score_gemma":0.0032818832,"teacher_disagreement_score":0.003943112,"about_ca_system_score_codex":0.00043133475,"about_ca_system_score_gemma":0.0002799952,"threshold_uncertainty_score":0.008917272},"labels":[],"label_agreement":null},{"id":"W2090851195","doi":"10.1016/j.jns.2012.03.025","title":"Hereditary spastic paraplegias with autosomal dominant, recessive, X-linked, or maternal trait of inheritance","year":2012,"lang":"en","type":"review","venue":"Journal of the Neurological Sciences","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":277,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Canadian Nautical Research Society","funders":"","keywords":"Hereditary spastic paraplegia; Genetics; Genetic heterogeneity; Spastic; Medicine; Biology; Gene; Phenotype; Physical medicine and rehabilitation","score_opus":0.12012251392632675,"score_gpt":0.32852320049933725,"score_spread":0.2084006865730105,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2090851195","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":[0.00022284516,0.9984882,0.00018602214,0.00012634064,0.00010746706,0.000003450529,0.000022625378,0.000009212755,0.00083379826],"genre_scores_gemma":[0.0013506975,0.99763227,0.00022931985,0.00009548002,0.0001572192,0.0000038494195,0.00004625737,0.00000149801,0.00048347784],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.99983263,0.000021594145,0.000033867258,0.000033795117,0.000058947546,0.00001909495],"domain_scores_gemma":[0.9997316,0.0001182406,0.00005723328,0.0000091327565,0.000052753636,0.00003102368],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00038029635,0.0012077654,0.00198428,0.0031287964,0.0002519003,0.000761002,0.0012933107,0.00086779083,0.0030975419],"category_scores_gemma":[0.0006095332,0.00021697643,0.00038743918,0.0028824976,0.0005759202,0.0009953628,0.00056597573,0.0010005049,0.0017580002],"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":[0.000098291675,0.00006852311,0.0006531594,0.013795509,0.00016365839,0.0027580033,0.000049105478,0.00031894026,0.0014834943,0.0020618828,0.031061685,0.9474877],"study_design_scores_gemma":[0.000064507956,0.00009844266,0.004654135,0.005724012,0.0005630196,0.041566916,0.0001969517,0.00018576333,0.0010826028,0.002802098,0.9430024,0.000059034086],"about_ca_topic_score_codex":0.0012700798,"about_ca_topic_score_gemma":0.0027094318,"teacher_disagreement_score":0.0031287964,"about_ca_system_score_codex":0.00049939816,"about_ca_system_score_gemma":0.0009481835,"threshold_uncertainty_score":0.0103622675},"labels":[],"label_agreement":null},{"id":"W2091348110","doi":"10.1111/j.1468-1331.2008.02117.x","title":"Refinement of the SPG9 locus on chromosome 10q23.3‐24.2 and exclusion of candidate genes","year":2008,"lang":"en","type":"article","venue":"European Journal of Neurology","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":7,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Hôpital Notre-Dame","funders":"Agence Nationale de la Recherche","keywords":"Locus (genetics); Candidate gene; Genetics; Hereditary spastic paraplegia; Gene; Positional cloning; Biology; Genetic heterogeneity; Disease gene identification; Exome sequencing; Phenotype","score_opus":0.04017614693495326,"score_gpt":0.23129340820679276,"score_spread":0.1911172612718395,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2091348110","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":[0.9945075,0.0004953255,0.0028200084,0.00016322,0.000030597344,0.000054859196,0.00065516937,0.00008534773,0.001188088],"genre_scores_gemma":[0.9881937,0.0004312384,0.006403464,0.0001622141,0.000039165727,0.00007396725,0.0030783971,0.00004171007,0.0015761624],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.99974257,0.000043865435,0.000018775003,0.000090774956,0.00006775079,0.0000362563],"domain_scores_gemma":[0.99956053,0.00015496353,0.000120397526,0.000047198737,0.000039147453,0.000077695346],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00026866415,0.0010245406,0.00049767556,0.00072240114,0.00032685965,0.00030936155,0.0006640637,0.0006098066,0.0035895342],"category_scores_gemma":[0.0007421407,0.00023021811,0.00069784385,0.00046553402,0.0003997571,0.000095611096,0.00036945188,0.000855824,0.00087628094],"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":[0.001689485,0.00023993276,0.07781515,0.0002897494,0.00034793146,0.024557622,0.00039041616,0.0015595943,0.8630985,0.0006065897,0.0010277472,0.02837723],"study_design_scores_gemma":[0.00059999665,0.00097423076,0.80159795,0.00018763205,0.0007540055,0.04878918,0.0002608573,0.0033403493,0.1215204,0.0008975608,0.021009129,0.00006868694],"about_ca_topic_score_codex":0.0022922843,"about_ca_topic_score_gemma":0.0034072322,"teacher_disagreement_score":0.0035895342,"about_ca_system_score_codex":0.0003724633,"about_ca_system_score_gemma":0.0004581515,"threshold_uncertainty_score":0.01200819},"labels":[],"label_agreement":null},{"id":"W2092659348","doi":"10.1212/wnl.61.7.1005","title":"<i>PS1</i> Alzheimer’s disease family with spastic paraplegia","year":2003,"lang":"en","type":"article","venue":"Neurology","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":28,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Xerox (Canada)","funders":"","keywords":"Hereditary spastic paraplegia; Spastic; Paraplegia; Mutation; Gene; Degenerative disease; Disease; Genetics; Coding region; Medicine; Biology; Pathology; Phenotype; Physical therapy; Psychiatry; Spinal cord","score_opus":0.043789799205826825,"score_gpt":0.25016991003481837,"score_spread":0.20638011082899155,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2092659348","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":[0.96718496,0.0006595895,0.0033535264,0.002550913,0.00027082328,0.000077579665,0.0005697198,0.00023397293,0.025098817],"genre_scores_gemma":[0.99071467,0.00041018316,0.0013096246,0.0007541348,0.00019897067,0.00001988084,0.00022943314,0.00003331415,0.0063296678],"study_design_codex":"case_report","study_design_gemma":"case_report","domain_scores_codex":[0.9998061,0.000029514096,0.000018910723,0.00004887935,0.000046688354,0.00004983471],"domain_scores_gemma":[0.9996791,0.0000887761,0.000058850306,0.000023565899,0.00005044883,0.00009925238],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00024763984,0.001309504,0.00041386118,0.00074816844,0.0023926287,0.00034999388,0.0004217962,0.0007946251,0.0041804966],"category_scores_gemma":[0.00091113406,0.000291504,0.000408147,0.0005746353,0.00075706886,0.00037504456,0.0005999468,0.0008712773,0.000997283],"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":[0.0009000415,0.00093908916,0.10301417,0.00016245854,0.00023346825,0.7503098,0.0042506317,0.00076433335,0.052175798,0.007843877,0.019250408,0.06015592],"study_design_scores_gemma":[0.00010143574,0.0005442466,0.09805419,0.00010248119,0.00017887857,0.8583426,0.000547109,0.0010293437,0.013279645,0.004088833,0.023649186,0.00008215346],"about_ca_topic_score_codex":0.004568626,"about_ca_topic_score_gemma":0.004435264,"teacher_disagreement_score":0.004568626,"about_ca_system_score_codex":0.00043123506,"about_ca_system_score_gemma":0.00046197211,"threshold_uncertainty_score":0.013985157},"labels":[],"label_agreement":null},{"id":"W2097806259","doi":"10.1139/g08-078","title":"Refinement of the locus for distal hereditary motor neuronopathy VII (dHMN-VII) and exclusion of candidate genes","year":2008,"lang":"en","type":"article","venue":"Genome","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":7,"is_retracted":false,"has_abstract":true,"route_ca_aff":false,"route_ca_fund":false,"route_ca_venue":true,"route_about_ca":false,"ca_institutions":"","funders":"Newlife the Charity for Disabled Children","keywords":"Biology; Genetics; Locus (genetics); Gene; Candidate gene","score_opus":0.026016458796180673,"score_gpt":0.22531777493810126,"score_spread":0.1993013161419206,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2097806259","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":[0.98684293,0.0005390376,0.009885331,0.00014951128,0.000021303986,0.00006672766,0.00041969222,0.00010282897,0.0019727042],"genre_scores_gemma":[0.9585368,0.00064358907,0.036488015,0.00011154119,0.000029592424,0.00007262222,0.0022111267,0.000092209,0.0018145327],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9996809,0.000063630345,0.000029768442,0.00008270573,0.00009875422,0.00004424408],"domain_scores_gemma":[0.9995722,0.0001915491,0.00006478289,0.00005751764,0.000045393273,0.00006849592],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0004157717,0.0007243013,0.0008983655,0.0007098909,0.00031850018,0.00040373084,0.00051297445,0.00037970277,0.0017604907],"category_scores_gemma":[0.0012516272,0.00026303786,0.0006473797,0.00036685055,0.00030659686,0.00016528658,0.00089135347,0.0008737881,0.0005847522],"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":[0.0012037818,0.00028162362,0.02724769,0.00018266987,0.0002090553,0.0079118395,0.00042910376,0.0038534647,0.90536374,0.002682858,0.00042752808,0.050206672],"study_design_scores_gemma":[0.0009685055,0.002304462,0.47716042,0.00031784322,0.0012913228,0.047396693,0.000740098,0.022305267,0.39085248,0.0050100298,0.05140321,0.00024971177],"about_ca_topic_score_codex":0.0016942162,"about_ca_topic_score_gemma":0.0031540692,"teacher_disagreement_score":0.0017604907,"about_ca_system_score_codex":0.00033247238,"about_ca_system_score_gemma":0.0003994105,"threshold_uncertainty_score":0.0058894157},"labels":[],"label_agreement":null},{"id":"W2097982305","doi":"10.1007/978-3-319-07311-8_4","title":"The Axon: Normal Structure and Pathological Alterations","year":2014,"lang":"en","type":"book-chapter","venue":"","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":5,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Toronto; Sunnybrook Health Science Centre; St. Michael's Hospital","funders":"","keywords":"Pathological; Neuroscience; Axon; Biology; Medicine; Pathology","score_opus":0.02881283551360083,"score_gpt":0.2299940304651468,"score_spread":0.20118119495154596,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2097982305","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":[0.0016644292,0.34471756,0.015296034,0.0043676724,0.009172543,0.000052893083,0.00042535554,0.00032067188,0.62398285],"genre_scores_gemma":[0.009876798,0.2039092,0.008972179,0.0023781254,0.0035705697,0.00009133612,0.00047808076,0.0001756937,0.77054805],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.9998802,0.0000140769125,0.00000661122,0.000019003424,0.000067693465,0.000012441233],"domain_scores_gemma":[0.999918,0.000039095215,0.0000050651015,0.000006710477,0.000022325228,0.000008956945],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00016531762,0.000940696,0.0005386588,0.0015191481,0.00047274938,0.0015071428,0.00069457915,0.0013231252,0.0131583335],"category_scores_gemma":[0.00028283868,0.0002611221,0.0002548222,0.0012452672,0.0012772408,0.002023918,0.0010417893,0.001571951,0.007849692],"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":[0.00003871704,0.000041526226,0.000120499346,0.00079441565,0.000008674637,0.00037358358,0.00029433746,0.00086799834,0.0026352794,0.15655592,0.3846555,0.45361355],"study_design_scores_gemma":[0.000002646296,0.000011881793,0.00022728027,0.0003331167,0.0000039651236,0.0009083914,0.000079437355,0.00014078573,0.00038909685,0.043718133,0.9541753,0.000010022998],"about_ca_topic_score_codex":0.0012696644,"about_ca_topic_score_gemma":0.0033391612,"teacher_disagreement_score":0.0131583335,"about_ca_system_score_codex":0.00080271286,"about_ca_system_score_gemma":0.0008663161,"threshold_uncertainty_score":0.044018984},"labels":[],"label_agreement":null},{"id":"W2098136807","doi":"10.1002/mds.20494","title":"Clinical and genetic study of a large <i>SPG4</i> Italian family","year":2005,"lang":"en","type":"article","venue":"Movement Disorders","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":33,"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 Health Network; Toronto Western Hospital; Occupational Cancer Research Centre; University of Toronto","funders":"","keywords":"Spasticity; Hereditary spastic paraplegia; Medicine; Peripheral neuropathy; Family history; Exon; Genetic heterogeneity; Genetics; Phenotype; Pediatrics; Physical medicine and rehabilitation; Biology; Internal medicine; Gene; Diabetes mellitus; Endocrinology","score_opus":0.035306571479347834,"score_gpt":0.313057859388643,"score_spread":0.27775128790929515,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2098136807","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":[0.9977385,0.00013331683,0.00036193698,0.00014263346,0.000013134968,0.000035694702,0.0001745911,0.000018197929,0.0013820687],"genre_scores_gemma":[0.9982243,0.00019443461,0.00054691435,0.00010838028,0.00004717337,0.000029204477,0.000287153,0.000014125488,0.00054833054],"study_design_codex":"case_report","study_design_gemma":"observational","domain_scores_codex":[0.99966717,0.00007078553,0.00002544525,0.000119281605,0.000065011365,0.000052199757],"domain_scores_gemma":[0.9995146,0.00013054027,0.00010457413,0.00003594983,0.00005388891,0.00016050987],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0003925558,0.0022407358,0.0006086178,0.0015152437,0.0014069967,0.0004913459,0.00068489293,0.0010306888,0.0022463559],"category_scores_gemma":[0.001862859,0.00049718836,0.00067895,0.00080684706,0.0013513499,0.00024144725,0.00079714536,0.00072426855,0.00047581957],"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":[0.00076311285,0.00053318514,0.30757713,0.000121830184,0.00022161548,0.63456595,0.0029264365,0.00062701805,0.03568099,0.0006325728,0.001968769,0.014381335],"study_design_scores_gemma":[0.00014399373,0.00093908334,0.41997308,0.0000634752,0.00022538009,0.57049215,0.0006411921,0.0011025321,0.0023202163,0.0003784233,0.0036600998,0.000060445323],"about_ca_topic_score_codex":0.0066849403,"about_ca_topic_score_gemma":0.0033049423,"teacher_disagreement_score":0.0066849403,"about_ca_system_score_codex":0.0007126552,"about_ca_system_score_gemma":0.0006062571,"threshold_uncertainty_score":0.013292015},"labels":[],"label_agreement":null},{"id":"W2098945832","doi":"10.1007/s10048-013-0366-9","title":"Autosomal recessive hereditary spastic paraplegia—clinical and genetic characteristics of a well-defined cohort","year":2013,"lang":"en","type":"article","venue":"Neurogenetics","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":38,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"North York General Hospital; Children's Hospital of Eastern Ontario; Hospital for Sick Children; London Health Sciences Centre; McMaster University; University of Toronto","funders":"National Institutes of Health","keywords":"Hereditary spastic paraplegia; Cohort; Human genetics; Genetic testing; Medicine; Spastic; Disease; Genetics; Pediatrics; Pathology; Internal medicine; Biology; Gene; Phenotype; Physical therapy","score_opus":0.028857337288388497,"score_gpt":0.2670532783197471,"score_spread":0.23819594103135863,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2098945832","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":[0.9989011,0.00011990996,0.00012714705,0.000030434207,0.000005715883,0.000014364111,0.00029148138,0.0000038717117,0.0005058984],"genre_scores_gemma":[0.998509,0.00012774143,0.00010173436,0.000035374745,0.0000232457,0.00002417364,0.0008638769,0.000008764135,0.0003061708],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99904686,0.0001727469,0.000107298445,0.00036134158,0.00013884471,0.00017292147],"domain_scores_gemma":[0.998877,0.00018337881,0.00026490897,0.0001432335,0.00015598032,0.00037549963],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0004736902,0.0008558163,0.0008720335,0.00188055,0.0020279768,0.0011127616,0.0009042878,0.0007224693,0.0040439675],"category_scores_gemma":[0.0024545128,0.0004921117,0.00061871635,0.0013126357,0.0008421844,0.0008147466,0.0014684448,0.00066554436,0.00071780913],"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":[0.0005524533,0.0002960235,0.9874791,0.0000121245375,0.00011355346,0.0052508092,0.0008159714,0.000065618435,0.0025386133,0.00019306922,0.00039611626,0.002286533],"study_design_scores_gemma":[0.00004336562,0.0003313822,0.9833784,0.000012761427,0.0000641799,0.01384087,0.0012141294,0.00019503672,0.00017946595,0.00015550439,0.0005646072,0.000020421718],"about_ca_topic_score_codex":0.005003585,"about_ca_topic_score_gemma":0.0041822656,"teacher_disagreement_score":0.005003585,"about_ca_system_score_codex":0.00035896327,"about_ca_system_score_gemma":0.00054030144,"threshold_uncertainty_score":0.013528407},"labels":[],"label_agreement":null},{"id":"W2100500106","doi":"10.1074/jbc.275.7.4537","title":"A Tripartite Nuclear Localization Signal in the PDZ-domain Protein L-periaxin","year":2000,"lang":"en","type":"article","venue":"Journal of Biological Chemistry","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":67,"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":"University of Leeds; University of Oxford","keywords":"PDZ domain; Schwann cell; Biology; Nucleus; Cell biology; Peripheral nervous system; Myelin; Nuclear localization sequence; Embryonic stem cell; Nervous system; Central nervous system; Neuroscience; Gene; Genetics","score_opus":0.030517772844489588,"score_gpt":0.2424475525897269,"score_spread":0.2119297797452373,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2100500106","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":[0.97167397,0.0031638395,0.019262431,0.0005681653,0.00017064599,0.00010947412,0.0007248454,0.00028570901,0.0040409244],"genre_scores_gemma":[0.98058736,0.00043752455,0.009122217,0.000263834,0.000028124156,0.000080838865,0.0017337585,0.000043890053,0.0077024014],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99981695,0.00003592653,0.000012708383,0.000052401512,0.000045004283,0.00003696293],"domain_scores_gemma":[0.9998104,0.000023079801,0.000045163502,0.000024698986,0.000014911661,0.00008180292],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0001965798,0.00034089264,0.00014240199,0.00020750525,0.00032163764,0.00029358576,0.00028302398,0.00048421542,0.0022880188],"category_scores_gemma":[0.00017425466,0.00022577385,0.00037184512,0.00013302494,0.00043232786,0.00031899856,0.0006031932,0.0008698049,0.002254732],"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":[0.000096216085,0.000019561396,0.00011919176,0.000030652922,0.0000031255665,0.00013032669,0.000011981796,0.000048789614,0.9977222,0.0003059952,0.00009053106,0.0014214399],"study_design_scores_gemma":[0.00016817606,0.00051933405,0.011215942,0.00003438543,0.000030197489,0.0029344037,0.00005433822,0.0028581428,0.96048194,0.00042751207,0.021253984,0.000021624106],"about_ca_topic_score_codex":0.00031089698,"about_ca_topic_score_gemma":0.00051095197,"teacher_disagreement_score":0.0022880188,"about_ca_system_score_codex":0.00081685133,"about_ca_system_score_gemma":0.0003123587,"threshold_uncertainty_score":0.00765419},"labels":[],"label_agreement":null},{"id":"W2110526616","doi":"10.1016/j.ajhg.2012.10.017","title":"Mutations in DDHD2, Encoding an Intracellular Phospholipase A1, Cause a Recessive Form of Complex Hereditary Spastic Paraplegia","year":2012,"lang":"en","type":"article","venue":"The American Journal of Human Genetics","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":182,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"McGill University and Génome Québec Innovation Centre; Ottawa Hospital; Children's Hospital of Eastern Ontario; University of Ottawa","funders":"Canadian Institutes of Health Research; Radboud Universiteit","keywords":"Hereditary spastic paraplegia; Phenotype; Biology; Mutation; Neuroscience; Gene knockdown; Genetics; Spastic; Intracellular; Cell biology; Gene; Medicine; Psychiatry","score_opus":0.07856893916375017,"score_gpt":0.32583572887741835,"score_spread":0.24726678971366817,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2110526616","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":[0.99262685,0.00059691054,0.0025507875,0.00037541825,0.00006741076,0.000049661518,0.0008779056,0.0001324509,0.00272257],"genre_scores_gemma":[0.997509,0.00012846556,0.001065741,0.0000638542,0.000025477952,0.000011349979,0.00026786883,0.000023313622,0.00090488244],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9998017,0.000022902135,0.000027760043,0.000049192033,0.00007133561,0.00002707871],"domain_scores_gemma":[0.9996524,0.00010305134,0.00009867271,0.000013309438,0.000022553293,0.000110112014],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00014058691,0.0019007274,0.0005034918,0.0010237362,0.00047981378,0.00035714713,0.0003423532,0.00079924,0.0015331272],"category_scores_gemma":[0.0006528542,0.00023898379,0.00030067883,0.00067197264,0.0007036116,0.0001766193,0.00053393125,0.00047989332,0.0003113781],"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":[0.0022439389,0.00035042493,0.041014653,0.00040524898,0.0004113447,0.38761753,0.00077995425,0.002526027,0.5387442,0.0030957807,0.0043382007,0.018472703],"study_design_scores_gemma":[0.00093391497,0.0010785842,0.18755977,0.00012924601,0.000619051,0.6239799,0.0005531886,0.012408943,0.15837461,0.0026286945,0.011570379,0.00016375649],"about_ca_topic_score_codex":0.0022826241,"about_ca_topic_score_gemma":0.0026589218,"teacher_disagreement_score":0.0022826241,"about_ca_system_score_codex":0.00064342585,"about_ca_system_score_gemma":0.00032460075,"threshold_uncertainty_score":0.005128801},"labels":[],"label_agreement":null},{"id":"W2112974028","doi":"10.1001/archneur.61.6.849","title":"Hereditary Spastic Paraplegia","year":2004,"lang":"en","type":"letter","venue":"Archives of Neurology","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":90,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Toronto","funders":"","keywords":"Hereditary spastic paraplegia; Genetics; Missense mutation; Locus (genetics); Haplotype; Biology; Founder effect; Mutation; Genetic heterogeneity; Genetic linkage; Phenotype; Genotype; Gene","score_opus":0.03076321015054323,"score_gpt":0.24383976250016542,"score_spread":0.2130765523496222,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2112974028","genre_codex":"empirical","genre_gemma":"editorial","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"editorial","genre_consensus":null,"domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.98989606,0.0013967726,0.0011510699,0.00016586507,0.00003288245,0.00004536424,0.0004917008,0.000096936,0.0067233397],"genre_scores_gemma":[0.9976561,0.00034066784,0.00028594924,0.00007261307,0.000020816653,0.0000120443765,0.00039554865,0.0000041106846,0.0012120879],"study_design_codex":"observational","study_design_gemma":"case_report","domain_scores_codex":[0.9998517,0.000019613395,0.000011809797,0.00002846385,0.0000416431,0.000046806534],"domain_scores_gemma":[0.9997942,0.000042689982,0.000058898186,0.000012980656,0.000041043986,0.00005027841],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.000121621066,0.0007687836,0.00027909916,0.00048329227,0.00034339592,0.00013230022,0.00023622837,0.00022256655,0.0072644353],"category_scores_gemma":[0.0006165366,0.00007722913,0.00015274138,0.00044369086,0.00038693333,0.00009548746,0.00038203015,0.00016276668,0.0006450923],"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":[0.0010185054,0.00029406603,0.54871655,0.0009148222,0.0003642609,0.2574998,0.0010328415,0.0007523777,0.06193713,0.0029111777,0.007991418,0.116567105],"study_design_scores_gemma":[0.00014871344,0.0012588024,0.54682547,0.00014566233,0.0001719584,0.43175298,0.00022983465,0.0005137753,0.006137069,0.0010933066,0.011705688,0.000016708449],"about_ca_topic_score_codex":0.0018828721,"about_ca_topic_score_gemma":0.0016042794,"teacher_disagreement_score":0.0072644353,"about_ca_system_score_codex":0.00033264232,"about_ca_system_score_gemma":0.0003317932,"threshold_uncertainty_score":0.024301946},"labels":[],"label_agreement":null},{"id":"W2115899947","doi":"10.1136/jnnp.68.4.538j","title":"Peripheral Neuropathy in Childhood. Second Edition.","year":2000,"lang":"en","type":"article","venue":"Journal of Neurology Neurosurgery & Psychiatry","topic":"Hereditary Neurological Disorders","field":"Neuroscience","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":"Foothills Medical Centre; University of Calgary","funders":"","keywords":"LEAPS; Peripheral nerve; Peripheral neuropathy; Peripheral; Neuroscience; Medicine; History; Anatomy; Art history; Psychology; Internal medicine; Endocrinology","score_opus":0.011449037678198876,"score_gpt":0.22893191318708694,"score_spread":0.21748287550888806,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2115899947","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":[0.00053014176,0.952293,0.0006914747,0.002614927,0.014255323,0.000041101084,0.0008073996,0.00019611654,0.028570503],"genre_scores_gemma":[0.004998198,0.8617655,0.0023312299,0.0025795284,0.010383788,0.000111310124,0.002427827,0.00013873499,0.11526384],"study_design_codex":"not_applicable","study_design_gemma":"not_applicable","domain_scores_codex":[0.9996165,0.00004834677,0.000042432144,0.00005959801,0.00017742421,0.00005570636],"domain_scores_gemma":[0.99934596,0.0001462043,0.000120425524,0.000031716085,0.00023502608,0.000120611265],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00053456874,0.002469601,0.0024165486,0.0044848793,0.00044490703,0.0015300055,0.0014124378,0.0013324298,0.059749648],"category_scores_gemma":[0.0014917586,0.0005737922,0.00093298656,0.002945877,0.00059617567,0.001828647,0.0011731035,0.002553306,0.03715998],"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":[0.0000972332,0.000045536744,0.00058489887,0.0017993875,0.00003663806,0.0006232207,0.00015010432,0.0001895299,0.00041651414,0.00108917,0.6251447,0.369823],"study_design_scores_gemma":[0.000017855396,0.00003812189,0.0021493325,0.0016289161,0.000028096536,0.0066240705,0.00009964413,0.00008308906,0.000104965315,0.0014044832,0.9877993,0.000022059996],"about_ca_topic_score_codex":0.006274232,"about_ca_topic_score_gemma":0.010194267,"teacher_disagreement_score":0.059749648,"about_ca_system_score_codex":0.000936521,"about_ca_system_score_gemma":0.0016706366,"threshold_uncertainty_score":0.1998825},"labels":[],"label_agreement":null},{"id":"W2118765999","doi":"10.1093/hmg/ddt663","title":"Transgenic expression of neuronal dystonin isoform 2 partially rescues the disease phenotype of the dystonia musculorum mouse model of hereditary sensory autonomic neuropathy VI","year":2013,"lang":"en","type":"article","venue":"Human Molecular Genetics","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":37,"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; National Research Council Canada; Ottawa Hospital","funders":"Canadian Institutes of Health Research; Department of Science and Technology, Ministry of Science and Technology, India","keywords":"Biology; Dystonia; Transgene; Genetically modified mouse; Dysautonomia; Gene isoform; Neuroscience; Pathology; Genetics; Gene; Disease; Medicine","score_opus":0.027521292402639532,"score_gpt":0.23517310151000728,"score_spread":0.20765180910736775,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2118765999","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":[0.99264777,0.00083541573,0.0026517408,0.00011282011,0.00006317046,0.000075521755,0.0010133099,0.0002941569,0.0023061957],"genre_scores_gemma":[0.98003113,0.0011841417,0.0050688824,0.00008213414,0.000022070082,0.00012289504,0.0022380245,0.00010797513,0.011142623],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9997937,0.000026541353,0.0000326529,0.00005121682,0.000046577396,0.00004931104],"domain_scores_gemma":[0.9998129,0.000016836286,0.000059962884,0.000015444362,0.0000134556885,0.00008140102],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00016895792,0.0007872217,0.00039747672,0.0006158157,0.00016646982,0.00029593144,0.00041445438,0.0006236789,0.0014540851],"category_scores_gemma":[0.00011607341,0.00024728358,0.0004405229,0.00018944265,0.00024788833,0.00018880807,0.00023191758,0.0007587481,0.00063775294],"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":[0.00008972806,0.000046914687,0.00010971768,0.000033962056,0.00000829706,0.00012970902,0.00001353827,0.000081505015,0.99874914,0.00008757807,0.000053019485,0.0005967108],"study_design_scores_gemma":[0.0001480017,0.001535329,0.007790667,0.000047811696,0.00007969008,0.0016552057,0.000069422655,0.00298019,0.9800918,0.00012680412,0.0054577217,0.000017322045],"about_ca_topic_score_codex":0.0008932286,"about_ca_topic_score_gemma":0.001393148,"teacher_disagreement_score":0.0014540851,"about_ca_system_score_codex":0.000327167,"about_ca_system_score_gemma":0.00025538477,"threshold_uncertainty_score":0.0048643947},"labels":[],"label_agreement":null},{"id":"W2119124845","doi":"10.1002/ana.10089","title":"Charcot‐Marie‐Tooth disease and related neuropathies: Mutation distribution and genotype‐phenotype correlation","year":2001,"lang":"en","type":"article","venue":"Annals of Neurology","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":279,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Hospital for Sick Children","funders":"National Institute of Neurological Disorders and Stroke; National Institute of Diabetes and Digestive and Kidney Diseases","keywords":"Peripheral myelin protein 22; Mutation; Biology; Myelin; Genetics; Myelin basic protein; Gene duplication; Mutant; Phenotype; Molecular biology; Gene; Endocrinology; Central nervous system","score_opus":0.04345436302772088,"score_gpt":0.27890127164604855,"score_spread":0.23544690861832768,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2119124845","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":[0.99910045,0.00028034198,0.00012973684,0.00001631439,0.0000024387653,0.000007207303,0.00008638992,0.000006169891,0.000371049],"genre_scores_gemma":[0.99934834,0.00010583079,0.0001356235,0.000018436469,0.000008789698,0.000010444646,0.00015023153,0.000004807345,0.00021756714],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9995413,0.00008340303,0.0000628048,0.0001781331,0.00006878503,0.00006568354],"domain_scores_gemma":[0.99898654,0.00045640394,0.00021525263,0.00007792566,0.00008755813,0.00017631872],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0003365481,0.00047721996,0.00047935525,0.0014226576,0.00033218885,0.00044669377,0.0002753912,0.0007037467,0.0037953279],"category_scores_gemma":[0.0016337594,0.00031314557,0.0001900395,0.00079229515,0.00040240007,0.00022568408,0.00039150903,0.00028960145,0.0006579339],"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":[0.0011378257,0.0002533318,0.92401123,0.00006432545,0.00013904319,0.014395514,0.00052019884,0.0002890972,0.042964544,0.00022374433,0.0004512494,0.015549838],"study_design_scores_gemma":[0.00006917725,0.00023903335,0.9560566,0.000015094383,0.000055242133,0.040783547,0.00016540992,0.00046479143,0.0014438141,0.00013846927,0.000548337,0.000020548005],"about_ca_topic_score_codex":0.0013633592,"about_ca_topic_score_gemma":0.0009392617,"teacher_disagreement_score":0.0037953279,"about_ca_system_score_codex":0.00019176726,"about_ca_system_score_gemma":0.00015669763,"threshold_uncertainty_score":0.012696624},"labels":[],"label_agreement":null},{"id":"W2120317938","doi":"10.1354/vp.39-5-598","title":"Ganglioradiculitis (Sensory Neuronopathy) in a Dog: Clinical, Morphologic, and Immunohistochemical Findings","year":2002,"lang":"en","type":"article","venue":"Veterinary Pathology","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":12,"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":"Immunohistochemistry; Sensory system; Pathogenesis; Pathology; Mononuclear cell infiltration; Infiltration (HVAC); Antibody; Sensory nerve; Medicine; Peripheral blood mononuclear cell; Immune system; Disease; Biology; Neuroscience; Immunology","score_opus":0.13025700472384427,"score_gpt":0.3282112896190719,"score_spread":0.19795428489522765,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2120317938","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":[0.9978138,0.00051906804,0.00030192974,0.00011328512,0.000016276732,0.000024410256,0.00006305278,0.000017788587,0.0011304084],"genre_scores_gemma":[0.9990221,0.00029968587,0.00026905767,0.000054486827,0.000021978147,0.0000068581962,0.00007341884,0.0000030488836,0.0002492476],"study_design_codex":"case_report","study_design_gemma":"case_report","domain_scores_codex":[0.9998234,0.000018748982,0.000019335672,0.0000470096,0.000034176344,0.000057380967],"domain_scores_gemma":[0.99980146,0.00004037652,0.000041089086,0.000011722501,0.000022871463,0.00008245172],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00028348496,0.00074480113,0.0005933435,0.0009724212,0.0005941307,0.00033902697,0.0003791602,0.0013531863,0.00087571505],"category_scores_gemma":[0.0006646956,0.00039069695,0.00030783578,0.0002757154,0.0010731136,0.000485451,0.00041512243,0.00044928843,0.00033724622],"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":[0.00045665316,0.00029073405,0.08873362,0.00013243956,0.00005718956,0.84844637,0.0009209502,0.00030138306,0.05598128,0.0002448392,0.00039220494,0.00404235],"study_design_scores_gemma":[0.00006529995,0.0010494968,0.13467418,0.000023925615,0.000072109564,0.857102,0.00039045038,0.0007806595,0.004537211,0.00016090042,0.0011170196,0.00002684985],"about_ca_topic_score_codex":0.0023853714,"about_ca_topic_score_gemma":0.0028306204,"teacher_disagreement_score":0.0023853714,"about_ca_system_score_codex":0.0006011053,"about_ca_system_score_gemma":0.00026685264,"threshold_uncertainty_score":0.00474298},"labels":[],"label_agreement":null},{"id":"W2120848776","doi":"10.1212/wnl.0b013e3182698d8d","title":"Genetic dysfunction of <i>MT-ATP6</i> causes axonal Charcot-Marie-Tooth disease","year":2012,"lang":"en","type":"article","venue":"Neurology","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":111,"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; Canadian Institutes of Health Research; Wellcome Trust","keywords":"Mitochondrial DNA; Proband; Genetics; Mutation; Protein subunit; Biology; Mitochondrion; Gene; Medicine; Molecular biology","score_opus":0.03220241225252136,"score_gpt":0.243651144627354,"score_spread":0.21144873237483264,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2120848776","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":[0.9990717,0.00023569725,0.00016633075,0.000033143377,0.0000066657285,0.000007765235,0.00009129753,0.000013836706,0.00037350596],"genre_scores_gemma":[0.99919397,0.00018144416,0.00020520884,0.000025440942,0.000023372697,0.000005976165,0.00013969012,0.000004246057,0.00022065194],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9998148,0.000019384655,0.000018719003,0.000064025735,0.000050432638,0.000032691667],"domain_scores_gemma":[0.99975866,0.00006176309,0.00009153203,0.000009696845,0.000024501582,0.00005379982],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00014201524,0.00089093234,0.00031355605,0.0005680521,0.00057004235,0.00027950792,0.000306152,0.00046690504,0.0025268653],"category_scores_gemma":[0.0006126551,0.00019332005,0.0001862881,0.00060802436,0.00032060043,0.00012327815,0.00026551113,0.00030738444,0.00042596174],"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":[0.0020470282,0.00037282283,0.7363602,0.0003525963,0.00026344176,0.07645744,0.00065104355,0.00040921636,0.16745758,0.0002901781,0.0016205081,0.013717887],"study_design_scores_gemma":[0.00017769333,0.00064747076,0.8443465,0.00008277436,0.00023998771,0.13576917,0.00045807238,0.0010400291,0.014557158,0.00020237651,0.0024576886,0.000021082546],"about_ca_topic_score_codex":0.0017660235,"about_ca_topic_score_gemma":0.002031396,"teacher_disagreement_score":0.0025268653,"about_ca_system_score_codex":0.00026111287,"about_ca_system_score_gemma":0.00014841955,"threshold_uncertainty_score":0.00845325},"labels":[],"label_agreement":null},{"id":"W2121587342","doi":"10.1093/brain/awp325","title":"SPATACSIN mutations cause autosomal recessive juvenile amyotrophic lateral sclerosis","year":2010,"lang":"en","type":"article","venue":"Brain","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":263,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":true,"ca_institutions":"Occupational Cancer Research Centre; University of Toronto","funders":"Consiglio Nazionale delle Ricerche; Ministero della Salute; Canada Excellence Research Chairs, Government of Canada; Wellcome Trust","keywords":"Hereditary spastic paraplegia; Amyotrophic lateral sclerosis; Corpus callosum; Medicine; Pathology; Mutation; Genetics; Biology; Disease; Gene; Phenotype","score_opus":0.04428999789423352,"score_gpt":0.2719914424342819,"score_spread":0.2277014445400484,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2121587342","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":[0.9992482,0.00023027777,0.00011694465,0.000011698842,0.000002369707,0.000006268117,0.00003885371,0.000013691088,0.0003315706],"genre_scores_gemma":[0.9993135,0.00017697403,0.00014225663,0.000020629055,0.0000061851174,0.00000385871,0.00007270283,0.000003850813,0.00026021464],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9998036,0.000030523122,0.000024618956,0.000041318817,0.000061683335,0.000038180107],"domain_scores_gemma":[0.99978083,0.000043256474,0.000090468086,0.000013677016,0.000019500847,0.000052180207],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00017899349,0.0006656284,0.00033582092,0.00052204245,0.00035878827,0.00016789463,0.00016992167,0.00026336507,0.0009947409],"category_scores_gemma":[0.0004557058,0.0001755523,0.0001805296,0.00031207057,0.00041118334,0.00009939451,0.00031200214,0.00017804367,0.00024249489],"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":[0.0016582026,0.00034954055,0.35121247,0.0002949472,0.00039565924,0.21169266,0.0016425564,0.0007410476,0.40154448,0.0005129035,0.0011714698,0.028784007],"study_design_scores_gemma":[0.00016470412,0.0012016656,0.7508743,0.00005273193,0.00022509055,0.21697547,0.00047827957,0.00074383634,0.02551617,0.0003965111,0.0033351183,0.000036198948],"about_ca_topic_score_codex":0.0023468828,"about_ca_topic_score_gemma":0.004482495,"teacher_disagreement_score":0.0023468828,"about_ca_system_score_codex":0.00034478644,"about_ca_system_score_gemma":0.0002896868,"threshold_uncertainty_score":0.0046664476},"labels":[],"label_agreement":null},{"id":"W2123079249","doi":"10.1111/jns5.12047","title":"Is carpal tunnel decompression warranted for <scp>HNPP</scp>?","year":2013,"lang":"en","type":"article","venue":"Journal of the Peripheral Nervous System","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":20,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Calgary","funders":"","keywords":"Medicine; Decompression; Carpal tunnel syndrome; Remyelination; Carpal tunnel; Surgical decompression; Entrapment Neuropathy; Surgery; Myelin; Internal medicine; Central nervous system","score_opus":0.030729117260410128,"score_gpt":0.25365960497779083,"score_spread":0.2229304877173807,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2123079249","genre_codex":"empirical","genre_gemma":"commentary","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"commentary","genre_consensus":null,"domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.92990416,0.0066217096,0.0015087664,0.034583233,0.00068561034,0.0001039513,0.00017453634,0.00014959327,0.026268411],"genre_scores_gemma":[0.9931431,0.0015094691,0.0009863747,0.0027369,0.00084013207,0.000014892435,0.00007929451,0.000013557801,0.0006763842],"study_design_codex":"case_report","study_design_gemma":"not_applicable","domain_scores_codex":[0.9996693,0.000042139913,0.000044485532,0.000059467846,0.00007022967,0.000114429255],"domain_scores_gemma":[0.9985409,0.0005379007,0.0003490172,0.000048007467,0.00015446656,0.0003697662],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0003823014,0.00033531114,0.00056665856,0.00052426796,0.0010128953,0.00069626846,0.00071529514,0.005489355,0.0027293556],"category_scores_gemma":[0.0037990871,0.00016226615,0.00038686916,0.00041024134,0.001202579,0.0011945616,0.00024025016,0.0010438608,0.00051499926],"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":[0.0023703587,0.000341435,0.38470152,0.0006798604,0.00011884763,0.4965106,0.0006628147,0.0015798848,0.02013356,0.0014770508,0.00894549,0.0824785],"study_design_scores_gemma":[0.00018051382,0.0013138102,0.24754156,0.00056652067,0.00012097899,0.72461426,0.0036732901,0.0034456938,0.005069725,0.004351852,0.008974437,0.00014732209],"about_ca_topic_score_codex":0.0033966058,"about_ca_topic_score_gemma":0.006373093,"teacher_disagreement_score":0.005489355,"about_ca_system_score_codex":0.0008243741,"about_ca_system_score_gemma":0.0015276333,"threshold_uncertainty_score":0.009130597},"labels":[],"label_agreement":null},{"id":"W2124720748","doi":"10.1093/brain/awv143","title":"Alteration of ornithine metabolism leads to dominant and recessive hereditary spastic paraplegia","year":2015,"lang":"en","type":"article","venue":"Brain","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":104,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"McGill University; Montreal Neurological Institute and Hospital","funders":"National Institute of Neurological Disorders and Stroke","keywords":"Hereditary spastic paraplegia; Compound heterozygosity; Ornithine; Genetics; Exome sequencing; Glutamine; Mutation; Biology; Medicine; Phenotype; Internal medicine; Arginine; Gene; Amino acid","score_opus":0.04711361153053879,"score_gpt":0.28834377940611833,"score_spread":0.24123016787557955,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2124720748","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":[0.9947667,0.0013265647,0.0012628994,0.000070595626,0.000014392549,0.000027021853,0.00033983868,0.00010794505,0.0020841402],"genre_scores_gemma":[0.9979589,0.00042386577,0.0005361319,0.000040015904,0.000012629049,0.000006595887,0.00022496938,0.000016176276,0.0007806195],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9997458,0.00004645579,0.000033985707,0.000073999414,0.00005791709,0.00004185567],"domain_scores_gemma":[0.99980694,0.00004132774,0.000062212464,0.000015090794,0.000017016362,0.000057345285],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00014488531,0.0014407885,0.00031510205,0.0005494766,0.00023389107,0.00019135722,0.00023830416,0.00030711907,0.0021997257],"category_scores_gemma":[0.0004087433,0.00016404431,0.00022740819,0.00038228297,0.0002585891,0.000086988504,0.0004768553,0.00019918065,0.00044066194],"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":[0.0014454204,0.00026369165,0.07086148,0.00054520415,0.0003203484,0.11539813,0.00048674125,0.00075660355,0.76430887,0.0010645519,0.001719156,0.04282978],"study_design_scores_gemma":[0.0002589555,0.0014780205,0.4356196,0.00016217698,0.00062689884,0.37669715,0.00029538258,0.004040107,0.16697535,0.0007302037,0.013060529,0.00005555449],"about_ca_topic_score_codex":0.0011909361,"about_ca_topic_score_gemma":0.001689713,"teacher_disagreement_score":0.0021997257,"about_ca_system_score_codex":0.00031417937,"about_ca_system_score_gemma":0.00020704852,"threshold_uncertainty_score":0.007358849},"labels":[],"label_agreement":null},{"id":"W2128711089","doi":"10.1007/s10048-014-0426-9","title":"The LITAF/SIMPLE I92V sequence variant results in an earlier age of onset of CMT1A/HNPP diseases","year":2014,"lang":"en","type":"article","venue":"Neurogenetics","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":22,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Trent University","funders":"Natural Sciences and Engineering Research Council of Canada","keywords":"Sequence (biology); Gene duplication; Biology; Genetics; Gene; Disease; Biomarker; Human genetics; Age of onset; Medicine; Pathology","score_opus":0.054934078581428736,"score_gpt":0.2951875233823061,"score_spread":0.24025344480087735,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2128711089","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":[0.9984409,0.00019557322,0.00035811125,0.00003781826,0.000015342279,0.0000073738624,0.00029261742,0.000018037188,0.0006342835],"genre_scores_gemma":[0.99852484,0.000095850955,0.00030176018,0.00004414919,0.000014128285,0.000007038223,0.00028255384,0.000016291591,0.0007133909],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.99984276,0.000024695262,0.000022596472,0.00006404713,0.000024810035,0.000021000033],"domain_scores_gemma":[0.9997042,0.000057733472,0.00012227902,0.000020120016,0.000021503236,0.000074224554],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00010080191,0.00059587625,0.00035910445,0.00063066557,0.00027608973,0.0002934808,0.00021486888,0.0005784806,0.004753185],"category_scores_gemma":[0.00051109516,0.0001496161,0.0003201838,0.0003771015,0.0002447872,0.00015632423,0.00027398302,0.00041422315,0.00071994454],"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":[0.0046479027,0.00053103466,0.21066563,0.00013682836,0.00029103793,0.03277832,0.0005483029,0.0005560527,0.7301899,0.0006661985,0.00089695345,0.018091805],"study_design_scores_gemma":[0.00011679108,0.0019740853,0.8277435,0.00006840475,0.00023806345,0.11295351,0.000438294,0.0015041435,0.05057035,0.0005438202,0.0037746476,0.00007441336],"about_ca_topic_score_codex":0.0011150355,"about_ca_topic_score_gemma":0.0006319381,"teacher_disagreement_score":0.004753185,"about_ca_system_score_codex":0.00014146394,"about_ca_system_score_gemma":0.00009636284,"threshold_uncertainty_score":0.01590097},"labels":[],"label_agreement":null},{"id":"W2129406491","doi":"10.1111/j.1525-1403.2009.00272.x","title":"Successful Treatment of Charcot-Marie-Tooth Chronic Pain with Spinal Cord Stimulation: A Case Study","year":2010,"lang":"en","type":"article","venue":"Neuromodulation Technology at the Neural Interface","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":4,"is_retracted":false,"has_abstract":false,"route_ca_aff":false,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":true,"ca_institutions":"","funders":"","keywords":"Medicine; McGill Pain Questionnaire; Chronic pain; Visual analogue scale; Spinal cord stimulation; Oswestry Disability Index; Quality of life (healthcare); Physical therapy; Spinal cord stimulator; Medical record; Spinal cord; Surgery; Low back pain; Alternative medicine","score_opus":0.03789887139245655,"score_gpt":0.31574620473651716,"score_spread":0.2778473333440606,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2129406491","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":[0.9468933,0.009206988,0.009224658,0.0066768224,0.0008132421,0.00043982032,0.0003628561,0.00029554046,0.02608669],"genre_scores_gemma":[0.98763627,0.0022577655,0.0029840004,0.0016808533,0.0008253523,0.00013908521,0.00010601711,0.000059341604,0.0043114955],"study_design_codex":"case_report","study_design_gemma":"case_report","domain_scores_codex":[0.9989778,0.00015722719,0.00010076032,0.00017528322,0.0001816802,0.00040728538],"domain_scores_gemma":[0.9987525,0.00052049663,0.00017025843,0.0001526491,0.00006224537,0.0003418504],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00051112805,0.0024465118,0.001679857,0.0027489876,0.005193257,0.0016693526,0.002605613,0.016959336,0.0025651495],"category_scores_gemma":[0.0039526015,0.0011047097,0.0029855743,0.0013306153,0.003348445,0.0013828389,0.0015249106,0.003213222,0.0011976144],"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":[0.000037106245,0.00016748438,0.0012561665,0.00002987955,0.000014553856,0.9958656,0.00011673265,0.00012735697,0.00047566657,0.00019184606,0.00011732203,0.0016002893],"study_design_scores_gemma":[0.000025989837,0.00015771069,0.0011589609,0.000011068954,0.000013362916,0.99735343,0.000060916474,0.00025415656,0.00050286413,0.00012901786,0.0003179306,0.000014509846],"about_ca_topic_score_codex":0.0021928134,"about_ca_topic_score_gemma":0.0033309148,"teacher_disagreement_score":0.016959336,"about_ca_system_score_codex":0.0019184484,"about_ca_system_score_gemma":0.0012874705,"threshold_uncertainty_score":0.013919413},"labels":[],"label_agreement":null},{"id":"W2133644189","doi":"10.1046/j.1529-8027.2002.2008_6.x","title":"PROGRESS IN CLINICAL NEUROSCIENCES: CHARCOT‐MARIE‐TOOTH DISEASE AND RELATED INHERITED PERIPHERAL NEUROPATHIES","year":2002,"lang":"en","type":"article","venue":"Journal of the Peripheral Nervous System","topic":"Hereditary Neurological Disorders","field":"Neuroscience","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":"Canadian Journal of Communication (Canada)","funders":"","keywords":"Tooth disease; Disease; Medicine; Pathological; Neuroscience; Genetic testing; Bioinformatics; Pathology; Psychology; Biology; Internal medicine","score_opus":0.040721458374855274,"score_gpt":0.270781484139664,"score_spread":0.23006002576480875,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2133644189","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":[0.005675784,0.95981824,0.0016724501,0.010854844,0.0023975496,0.000020466288,0.000024167579,0.00006646266,0.01946997],"genre_scores_gemma":[0.042617206,0.9297642,0.0029943676,0.0066987104,0.009177758,0.000032838037,0.00009370527,0.000023573153,0.008597739],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.9992902,0.0002517321,0.000098997145,0.000096409036,0.00019463313,0.00006801529],"domain_scores_gemma":[0.99845505,0.0006697101,0.0001943522,0.00006227219,0.0003713469,0.0002472225],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0020874965,0.00058386975,0.0008971923,0.0015958954,0.0005009572,0.0018793831,0.00047667354,0.001923461,0.0032082286],"category_scores_gemma":[0.00259233,0.00015403389,0.00022585822,0.0014591585,0.0014449753,0.0017994384,0.0007664344,0.001975383,0.0015427596],"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":[0.00016157787,0.00025241007,0.003367147,0.0025724082,0.000048609603,0.0019584561,0.00031371685,0.0002499204,0.0028170426,0.012137791,0.042539157,0.9335818],"study_design_scores_gemma":[0.000103041464,0.0007846824,0.024699248,0.00309515,0.00013695999,0.057729717,0.00085119426,0.0004908645,0.0015246458,0.019012308,0.89149636,0.000075825716],"about_ca_topic_score_codex":0.0012571465,"about_ca_topic_score_gemma":0.002254599,"teacher_disagreement_score":0.0032082286,"about_ca_system_score_codex":0.00097654434,"about_ca_system_score_gemma":0.001627642,"threshold_uncertainty_score":0.011039913},"labels":[],"label_agreement":null},{"id":"W2135916709","doi":"10.1242/dmm.010942","title":"Loss of the E3 ubiquitin ligase LRSAM1 sensitizes peripheral axons to degeneration in a mouse model of Charcot-Marie-Tooth disease","year":2013,"lang":"en","type":"article","venue":"Disease Models & Mechanisms","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":55,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Dalhousie University; Université de Montréal","funders":"National Institute of Neurological Disorders and Stroke","keywords":"Endosome; Lysosome; Biology; Cell biology; Axon; Ubiquitin ligase; Axoplasmic transport; Degeneration (medical); Colocalization; Transfection; Hereditary motor and sensory neuropathy; Ubiquitin; Neuroscience; Genetics; Intracellular; Pathology; Gene; Medicine; Biochemistry","score_opus":0.03562832794340157,"score_gpt":0.23595069830054058,"score_spread":0.200322370357139,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2135916709","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":[0.99384755,0.001292621,0.0015306589,0.00026442838,0.00007079329,0.00006651226,0.0004331799,0.0003394162,0.0021546974],"genre_scores_gemma":[0.9891177,0.0015840859,0.0028474932,0.0001515887,0.000020919426,0.00012039803,0.0004961311,0.00006939852,0.0055922917],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99962556,0.00007333712,0.000040771174,0.000091500464,0.00010707522,0.000061743674],"domain_scores_gemma":[0.9997607,0.00003333331,0.000071117094,0.0000283546,0.000015150688,0.00009130405],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00032521656,0.0010044461,0.0005701377,0.0011501071,0.0003364532,0.0004311666,0.0004483047,0.00092552026,0.0023264273],"category_scores_gemma":[0.00026043065,0.00052574044,0.00041999208,0.00030804248,0.00063186313,0.0003728349,0.0003826525,0.0012144072,0.0007236845],"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":[0.000210196,0.00012979175,0.00026611125,0.000059888887,0.000017725893,0.00038581016,0.000034519442,0.00014541061,0.9971764,0.00014879521,0.00014640874,0.0012789314],"study_design_scores_gemma":[0.0002533883,0.0039047925,0.012525389,0.00010267967,0.00012207057,0.0041435612,0.00012900772,0.0032906493,0.9693245,0.0005155189,0.0056510647,0.00003741336],"about_ca_topic_score_codex":0.00089969963,"about_ca_topic_score_gemma":0.001994761,"teacher_disagreement_score":0.0023264273,"about_ca_system_score_codex":0.00053117087,"about_ca_system_score_gemma":0.00029209626,"threshold_uncertainty_score":0.0077826977},"labels":[],"label_agreement":null},{"id":"W2140802077","doi":"10.1523/jneurosci.1081-12.2012","title":"Peripherin Is a Subunit of Peripheral Nerve Neurofilaments: Implications for Differential Vulnerability of CNS and Peripheral Nervous System Axons","year":2012,"lang":"en","type":"article","venue":"Journal of Neuroscience","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":164,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Centre hospitalier de l'Université Laval","funders":"National Institute on Aging","keywords":"Neurofilament; Peripherin; Peripheral nervous system; Neuroscience; Peripheral; Peripheral nerve; Central nervous system; Axon; Nervous system; Protein subunit; Vulnerability (computing); Biology; Medicine; Anatomy; Immunology; Computer science; Internal medicine","score_opus":0.06680013836651837,"score_gpt":0.31131652337443994,"score_spread":0.24451638500792156,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2140802077","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":[0.9908646,0.005568143,0.001706089,0.000081077786,0.000011029771,0.0000056156473,0.00018562414,0.00003884313,0.0015391527],"genre_scores_gemma":[0.99681586,0.0012210748,0.00086282217,0.000020890626,0.0000102135255,0.0000046047344,0.00013793744,0.0000060672337,0.00092061626],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.999941,0.0000057033867,0.0000047591216,0.000028122087,0.000010870564,0.000009542079],"domain_scores_gemma":[0.99987876,0.000016227548,0.000049847178,0.000006399683,0.000009975008,0.000038811246],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00013143774,0.00017813452,0.00014486542,0.0002744884,0.0001863565,0.0003036266,0.00013618001,0.00026173724,0.0010770521],"category_scores_gemma":[0.0001412794,0.00007840364,0.00009709836,0.00012989971,0.0002292598,0.00038112528,0.00025609872,0.00019664898,0.0001530296],"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":[0.0001621861,0.000006819029,0.0023033482,0.000057091052,0.000006534759,0.00021034648,0.000023143,0.000036151836,0.99455655,0.00013256194,0.000022772558,0.0024825607],"study_design_scores_gemma":[0.000026540993,0.0005416193,0.54172194,0.000046033776,0.000056090805,0.009738286,0.00025936865,0.0010789012,0.44115266,0.0007228195,0.004631399,0.0000243473],"about_ca_topic_score_codex":0.00017736304,"about_ca_topic_score_gemma":0.00025162616,"teacher_disagreement_score":0.0010770521,"about_ca_system_score_codex":0.00012237257,"about_ca_system_score_gemma":0.00005775114,"threshold_uncertainty_score":0.0036031008},"labels":[],"label_agreement":null},{"id":"W2142627450","doi":"10.1038/ng.2406","title":"Loss-of-function mutations in HINT1 cause axonal neuropathy with neuromyotonia","year":2012,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":129,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"London Health Sciences Centre; Western University","funders":"National Institute of Neurological Disorders and Stroke","keywords":"Neuromyotonia; Biology; Loss function; Function (biology); Neuroscience; Genetics; Phenotype; Gene","score_opus":0.024944830254755954,"score_gpt":0.2671345386423552,"score_spread":0.24218970838759923,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2142627450","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":[0.993586,0.000649092,0.001447845,0.00037228514,0.000091379465,0.000032250486,0.00031308827,0.00013851891,0.0033696601],"genre_scores_gemma":[0.99782604,0.00015697404,0.00088074995,0.000073929834,0.000028772016,0.0000074582154,0.0000678404,0.000025685498,0.0009324094],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.99983144,0.000025266629,0.000029337207,0.000027405644,0.00005344356,0.000033191838],"domain_scores_gemma":[0.99959725,0.00012648026,0.00011317751,0.000017882827,0.000029574392,0.00011560527],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00018335416,0.0015733037,0.00040880352,0.0008858842,0.0005305012,0.00038421425,0.0006309902,0.001325639,0.0023857425],"category_scores_gemma":[0.0006905477,0.00028665178,0.00043696858,0.00042722767,0.00084283226,0.0002774304,0.00061726477,0.0005705938,0.00045689804],"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":[0.0028406568,0.00037125754,0.053312145,0.00041567435,0.0004765603,0.3537168,0.0005598297,0.0038939384,0.5565615,0.0031980772,0.003291366,0.021362178],"study_design_scores_gemma":[0.00046793453,0.0009923643,0.3465163,0.0001412901,0.0011327629,0.44024885,0.0007634113,0.010257655,0.1896324,0.002976311,0.006668105,0.00020265023],"about_ca_topic_score_codex":0.0024723187,"about_ca_topic_score_gemma":0.00389515,"teacher_disagreement_score":0.0024723187,"about_ca_system_score_codex":0.00046422187,"about_ca_system_score_gemma":0.00033688036,"threshold_uncertainty_score":0.007981062},"labels":[],"label_agreement":null},{"id":"W2142757771","doi":"10.1177/0036933014554875","title":"Vitamin B12 deficiency causing night sweats","year":2014,"lang":"en","type":"article","venue":"Scottish Medical Journal","topic":"Hereditary Neurological Disorders","field":"Neuroscience","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":"Regina General Hospital","funders":"","keywords":"Medicine; Vitamin B12; Pediatrics; Physiology; Internal medicine","score_opus":0.023652394645771097,"score_gpt":0.2746124632415449,"score_spread":0.2509600685957738,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2142757771","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":[0.9536513,0.009303732,0.0017770807,0.0008599788,0.00026899643,0.000080508216,0.00033198943,0.00022119512,0.033505242],"genre_scores_gemma":[0.99510455,0.0014605118,0.00024049087,0.00040626185,0.000071594346,0.0000029737694,0.00007464318,0.000018679206,0.002620165],"study_design_codex":"case_report","study_design_gemma":"case_report","domain_scores_codex":[0.999846,0.0000134020365,0.000015703215,0.00002327172,0.000037077334,0.00006453206],"domain_scores_gemma":[0.99964345,0.00007742654,0.000100638594,0.000026471267,0.000045199216,0.00010676918],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.000086676344,0.0006700283,0.0004833091,0.00053102203,0.00081583153,0.0003606734,0.00026539218,0.0006422039,0.0029129288],"category_scores_gemma":[0.00093917036,0.00013870581,0.00033839067,0.0005421353,0.0005216239,0.00023875535,0.00036092414,0.0005178995,0.0006219272],"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":[0.00030298205,0.00012774506,0.13000967,0.00038632366,0.00008728688,0.77116853,0.0011784538,0.0001354304,0.045230277,0.001317172,0.004405346,0.045650702],"study_design_scores_gemma":[0.00004002549,0.00026138956,0.10074855,0.00006451545,0.000056788333,0.8804959,0.00047349505,0.00015855771,0.0074057803,0.0007403011,0.009522182,0.000032524484],"about_ca_topic_score_codex":0.0058947364,"about_ca_topic_score_gemma":0.006531934,"teacher_disagreement_score":0.0058947364,"about_ca_system_score_codex":0.00038774143,"about_ca_system_score_gemma":0.00031821913,"threshold_uncertainty_score":0.011720896},"labels":[],"label_agreement":null},{"id":"W2143717535","doi":"10.1096/fj.11-184911","title":"Specialization of endoplasmic reticulum chaperones for the folding and function of myelin glycoproteins P0 and PMP22","year":2011,"lang":"en","type":"article","venue":"The FASEB Journal","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":27,"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 Alberta","funders":"Canadian Institutes of Health Research; Alberta Innovates - Health Solutions","keywords":"Calnexin; Calreticulin; Endoplasmic reticulum; Myelin; Cell biology; Peripheral myelin protein 22; Glycoprotein; Protein disulfide-isomerase; Chaperone (clinical); Protein folding; Unfolded protein response; Function (biology); Biology; Chemistry; Biochemistry; Neuroscience; Medicine; Pathology","score_opus":0.060366318018191624,"score_gpt":0.23546798867070867,"score_spread":0.17510167065251706,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2143717535","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":[0.9979831,0.0005440429,0.0008556413,0.000055787503,0.000004667895,0.0000027565177,0.000024980593,0.00002199861,0.0005070283],"genre_scores_gemma":[0.99767655,0.00032878216,0.001030453,0.000027212727,0.000002701096,0.0000046899377,0.000086919346,0.000005776352,0.000836929],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9998946,0.000020832942,0.000008666509,0.00002407848,0.000025313255,0.000026449476],"domain_scores_gemma":[0.9998863,0.000010463193,0.000023284336,0.000019366935,0.000021272466,0.00003941386],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00018300622,0.00024646163,0.00016706072,0.00011869444,0.00014505313,0.00032565524,0.00014363081,0.000199391,0.0005197203],"category_scores_gemma":[0.00018793483,0.00008024334,0.00014206117,0.00007964384,0.00019463063,0.00025021896,0.00029111985,0.00021923355,0.00023763596],"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":[0.00005110364,0.000006354152,0.0005378893,0.000010809498,0.000002369261,0.00015128432,0.000008564286,0.000026155605,0.9983058,0.00012867588,0.000022277163,0.0007487288],"study_design_scores_gemma":[0.000026366568,0.00014355646,0.046411615,0.000009942429,0.000027455277,0.0033714145,0.000106198815,0.00219802,0.94441694,0.00036076602,0.0029183463,0.000009340057],"about_ca_topic_score_codex":0.00039870382,"about_ca_topic_score_gemma":0.00048507235,"teacher_disagreement_score":0.0005197203,"about_ca_system_score_codex":0.00027631645,"about_ca_system_score_gemma":0.00017736845,"threshold_uncertainty_score":0.0020048022},"labels":[],"label_agreement":null},{"id":"W2149004697","doi":"10.1523/jneurosci.2580-06.2006","title":"α-Internexin Is Structurally and Functionally Associated with the Neurofilament Triplet Proteins in the Mature CNS","year":2006,"lang":"en","type":"article","venue":"Journal of Neuroscience","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":217,"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 Laval; McGill University; Royal Victoria Hospital","funders":"National Institute on Aging","keywords":"Neurofilament; Protein subunit; Intermediate filament; Cell biology; Biology; Immunogold labelling; Alpha (finance); Chemistry; Cytoskeleton; Biophysics; Biochemistry; Cell; Anatomy; Gene; Immunology; Immunohistochemistry; Ultrastructure","score_opus":0.02326281858025546,"score_gpt":0.23614033254443628,"score_spread":0.2128775139641808,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2149004697","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":[0.99610484,0.0015657241,0.0013338662,0.00003090273,0.000011021936,0.000004586134,0.00014598595,0.000028705163,0.0007744092],"genre_scores_gemma":[0.9922219,0.0012040781,0.0017039741,0.000025483965,0.000013257724,0.000011903294,0.0006779948,0.000013223365,0.004128166],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9999318,0.000004014094,0.000005992733,0.000031317555,0.000016252354,0.000010737542],"domain_scores_gemma":[0.9998691,0.0000058823703,0.000057859696,0.000008537561,0.000013518468,0.000045127057],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.000066525674,0.00023127458,0.00013476974,0.00023707312,0.00016282598,0.00024599844,0.00014204504,0.00015144935,0.000744991],"category_scores_gemma":[0.00009214648,0.00010612778,0.00011428073,0.00015088519,0.00015153414,0.00026381973,0.00016489728,0.00027086367,0.00031573145],"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":[0.000052235187,0.0000052369137,0.0014174061,0.000011526271,0.0000032556886,0.00008370923,0.000011432102,0.000013845276,0.99721766,0.00005493095,0.000014371487,0.0011144729],"study_design_scores_gemma":[0.000015585327,0.00036353467,0.3584601,0.000033087093,0.000054958273,0.006307286,0.000147861,0.0009902935,0.623037,0.0003767709,0.010200824,0.00001271129],"about_ca_topic_score_codex":0.0004800052,"about_ca_topic_score_gemma":0.00059304223,"teacher_disagreement_score":0.000744991,"about_ca_system_score_codex":0.00026891913,"about_ca_system_score_gemma":0.00012080931,"threshold_uncertainty_score":0.002492249},"labels":[],"label_agreement":null},{"id":"W2149819117","doi":"10.4021/jnr.v2i6.154","title":"Analysis of Association of Deletion in the Repeat Region of the Periaxin Gene With Late Onset Motor Neuropathy","year":2013,"lang":"en","type":"article","venue":"Journal of Neurology Research","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":2,"is_retracted":false,"has_abstract":true,"route_ca_aff":false,"route_ca_fund":false,"route_ca_venue":true,"route_about_ca":false,"ca_institutions":"","funders":"","keywords":"Peripheral myelin protein 22; Medicine; Exon; Peripheral neuropathy; Genetics; Gene; Compound heterozygosity; Hereditary motor and sensory neuropathy; Mutation; Disease; Gene duplication; Pathology; Biology; Endocrinology; Diabetes mellitus","score_opus":0.06336105494776433,"score_gpt":0.31609522618893793,"score_spread":0.2527341712411736,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2149819117","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":[0.99940515,0.000054696116,0.00015069712,0.000014317349,0.000002163595,0.000005104273,0.00004145819,0.0000052110945,0.00032116385],"genre_scores_gemma":[0.9994518,0.00003391168,0.00019045593,0.000019216024,0.000006307151,0.000006129914,0.00010965372,0.0000027574827,0.00017965832],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99981004,0.00004716106,0.00002180498,0.000051878655,0.000033730084,0.000035355435],"domain_scores_gemma":[0.9992848,0.00025822583,0.00022574142,0.000032848802,0.000053616393,0.00014483083],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.000297986,0.0004652503,0.00018088955,0.0009560598,0.00035358674,0.00021215685,0.0003296888,0.0006061609,0.002357569],"category_scores_gemma":[0.0009736198,0.0001624733,0.00019275682,0.00030745775,0.00028289692,0.0001507398,0.000259332,0.00037394193,0.0003859933],"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":[0.00080552755,0.00037392695,0.85065955,0.000053918207,0.00006539696,0.06875093,0.0004727312,0.00018614871,0.07333846,0.00013520192,0.00019206027,0.0049661486],"study_design_scores_gemma":[0.00006469033,0.0012358353,0.80712926,0.000027256809,0.00010702262,0.17824084,0.00033459088,0.0007010804,0.011146452,0.00009449218,0.00089867995,0.000019922214],"about_ca_topic_score_codex":0.0006598432,"about_ca_topic_score_gemma":0.0006758702,"teacher_disagreement_score":0.002357569,"about_ca_system_score_codex":0.00013888355,"about_ca_system_score_gemma":0.00015860308,"threshold_uncertainty_score":0.007886887},"labels":[],"label_agreement":null},{"id":"W2150495344","doi":"10.1093/brain/awq168","title":"SH3TC2, a protein mutant in Charcot–Marie–Tooth neuropathy, links peripheral nerve myelination to endosomal recycling","year":2010,"lang":"en","type":"article","venue":"Brain","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":97,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Western University","funders":"Deutsche Forschungsgemeinschaft; Schweizerischer Nationalfonds zur Förderung der Wissenschaftlichen Forschung; University College Cork; RWTH Aachen University; Vanderbilt University Medical Center; Vanderbilt University; National Science Foundation","keywords":"Schwann cell; Endosome; Myelin; Cell biology; Peripheral nervous system; Biology; Peripheral neuropathy; Peripheral myelin protein 22; Neuroscience; Intracellular; Central nervous system; Endocrinology","score_opus":0.022476449653751226,"score_gpt":0.2634433029872639,"score_spread":0.2409668533335127,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2150495344","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":[0.99642414,0.00050723227,0.001384511,0.000117242955,0.000026316633,0.000025571644,0.00027781396,0.00009407144,0.0011429746],"genre_scores_gemma":[0.9964663,0.0003308951,0.0011788706,0.00006891886,0.000018995954,0.000022902615,0.0003883256,0.000030853684,0.0014939432],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99985266,0.00002537835,0.000017032857,0.000040846684,0.000041025174,0.00002303148],"domain_scores_gemma":[0.99983346,0.000041448515,0.000052064544,0.000009847993,0.000011915426,0.000051179497],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00018217092,0.0014220468,0.00029701824,0.000861976,0.00045563374,0.00020972807,0.0002468972,0.0006605243,0.002249512],"category_scores_gemma":[0.00025120907,0.00020651915,0.00034645305,0.00036207246,0.0007450723,0.00015480262,0.00039612007,0.00050215865,0.0003655881],"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":[0.0008312779,0.000121875186,0.004131758,0.000117067815,0.00010657306,0.0072445218,0.0001231393,0.0002540223,0.9809334,0.00038081134,0.0005479843,0.0052075465],"study_design_scores_gemma":[0.00060733326,0.0018241409,0.14762646,0.000116533265,0.00048787284,0.08218579,0.0002817675,0.008244157,0.7475862,0.0010940718,0.009856069,0.000089627196],"about_ca_topic_score_codex":0.0021808262,"about_ca_topic_score_gemma":0.003617742,"teacher_disagreement_score":0.002249512,"about_ca_system_score_codex":0.0004859653,"about_ca_system_score_gemma":0.00031114309,"threshold_uncertainty_score":0.0075253844},"labels":[],"label_agreement":null},{"id":"W2152589229","doi":"10.1093/hmg/ddi447","title":"Spastin and atlastin, two proteins mutated in autosomal-dominant hereditary spastic paraplegia, are binding partners","year":2005,"lang":"en","type":"article","venue":"Human Molecular Genetics","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":150,"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":"Medical Research Council; National Institutes of Health; Cambridge Commonwealth Trust; University of Toronto; National Science Council; Wellcome Trust","keywords":"Hereditary spastic paraplegia; Biology; Cell biology; Gene isoform; Genetics; Gene; Phenotype","score_opus":0.03638803331932904,"score_gpt":0.29588573974687876,"score_spread":0.2594977064275497,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2152589229","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":[0.99505335,0.0013929014,0.0023135326,0.000054765962,0.000011782469,0.000007783742,0.00028381645,0.00004235462,0.00083986646],"genre_scores_gemma":[0.99255776,0.00061759504,0.003605428,0.000050508366,0.0000058240785,0.0000141037435,0.0012960765,0.000011010036,0.0018417359],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99988747,0.000018755032,0.000009132125,0.000029100902,0.000039092345,0.000016416096],"domain_scores_gemma":[0.99990976,0.000015997055,0.00003199483,0.000006929035,0.0000075015532,0.000027860675],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00007901618,0.00044366784,0.00029040244,0.00025320367,0.00017430584,0.0002888682,0.0002516619,0.00031826372,0.0012523505],"category_scores_gemma":[0.00021563812,0.00017701853,0.00017787245,0.00023052233,0.0002566492,0.00019683225,0.00038970675,0.00029328364,0.0004947046],"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":[0.00008049772,0.000008829843,0.0009889544,0.00004722839,0.000008938563,0.00037172157,0.00002293815,0.0000867849,0.99642605,0.00020773319,0.000049600298,0.0017007247],"study_design_scores_gemma":[0.000035848716,0.00018616908,0.042861063,0.000017780505,0.000036414644,0.010075436,0.00011124522,0.0024201002,0.9366002,0.0005041635,0.007134743,0.000016858647],"about_ca_topic_score_codex":0.0005395822,"about_ca_topic_score_gemma":0.0011615797,"teacher_disagreement_score":0.0012523505,"about_ca_system_score_codex":0.0004855731,"about_ca_system_score_gemma":0.00015543835,"threshold_uncertainty_score":0.004189551},"labels":[],"label_agreement":null},{"id":"W2157927241","doi":"10.1096/fj.11-196345","title":"Normal role of the low‐molecular‐weight neurofilament protein in mitochondrial dynamics and disruption in Charcot‐Marie‐Tooth disease","year":2011,"lang":"en","type":"article","venue":"The FASEB Journal","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":65,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Centre hospitalier de l'Université Laval; Centre hospitalier universitaire de Québec; McGill University; Université Laval; Montreal Neurological Institute and Hospital","funders":"Canadian Institutes of Health Research; Muscular Dystrophy Association","keywords":"MFN2; Neurofilament; mitochondrial fusion; Mitochondrion; LMNA; Cell biology; Biology; Mutant; Intermediate filament; Cytoskeleton; Knockout mouse; Gene; Genetics; Mitochondrial DNA; Mutation; Cell; Immunology","score_opus":0.013455780145556429,"score_gpt":0.21122146803148512,"score_spread":0.1977656878859287,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2157927241","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":[0.9971521,0.0008305503,0.0014878938,0.000036033394,0.000010126571,0.000008735897,0.00012047647,0.000051008083,0.0003029636],"genre_scores_gemma":[0.9984748,0.0003110288,0.0007305282,0.000011344035,0.0000026533412,0.000010294383,0.0001068007,0.000007648458,0.00034498677],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99987805,0.000015355763,0.000022433565,0.00003318927,0.00003132495,0.000019621617],"domain_scores_gemma":[0.9998499,0.000016973914,0.000056607187,0.000012004119,0.00001794751,0.000046502915],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00015402977,0.00039999574,0.00020683956,0.00038199918,0.00018499259,0.00021489285,0.00018575971,0.00052016857,0.0003777591],"category_scores_gemma":[0.00022000435,0.00014873435,0.00017311411,0.00012514775,0.0003676961,0.00028488654,0.00025216053,0.00036341525,0.000115254064],"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":[0.000098511744,0.000009546478,0.00070825237,0.000013004809,0.0000033434803,0.00024465044,0.000015128517,0.00003388645,0.998351,0.000032110256,0.000009245187,0.00048128262],"study_design_scores_gemma":[0.000031245847,0.0005183239,0.09393369,0.000017580767,0.00004461812,0.007877437,0.00010883741,0.0014144083,0.8937811,0.00030585955,0.0019435545,0.000023312155],"about_ca_topic_score_codex":0.0007930623,"about_ca_topic_score_gemma":0.0008405846,"teacher_disagreement_score":0.0007930623,"about_ca_system_score_codex":0.0002791207,"about_ca_system_score_gemma":0.0001562637,"threshold_uncertainty_score":0.0020251274},"labels":[],"label_agreement":null},{"id":"W2158864404","doi":"10.1017/s0317167100013263","title":"A Novel <i>PLP1</i> Mutation Further Expands the Clinical Heterogeneity at the Locus","year":2012,"lang":"en","type":"article","venue":"Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":7,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":true,"route_about_ca":true,"ca_institutions":"Montreal Heart Institute; Université de Montréal; McGill University Health Centre; Montreal Children's Hospital","funders":"Canadian Institutes of Health Research","keywords":"Genetics; Locus (genetics); Proteolipid protein 1; Genetic linkage; Missense mutation; Spasticity; Genetic heterogeneity; Proband; Biology; Hereditary spastic paraplegia; Gene; Mutation; Medicine; Phenotype; Myelin; Neuroscience; Myelin basic protein; Physical medicine and rehabilitation","score_opus":0.10212992524389086,"score_gpt":0.3291161134260448,"score_spread":0.22698618818215394,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2158864404","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":[0.9919927,0.0004226219,0.00164942,0.0007016308,0.000031738717,0.000062730636,0.00053883623,0.00014381208,0.0044564013],"genre_scores_gemma":[0.99680316,0.00019805465,0.0015079371,0.00014321036,0.000037574686,0.000015268926,0.00034002293,0.000026398297,0.0009282276],"study_design_codex":"case_report","study_design_gemma":"case_report","domain_scores_codex":[0.9998368,0.000008501958,0.000011486684,0.00006115482,0.000034445384,0.00004764909],"domain_scores_gemma":[0.99970955,0.000087141496,0.000063463034,0.000014544179,0.000037652346,0.000087550914],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00014306902,0.0015162302,0.00037622004,0.000698681,0.0010530961,0.0005124965,0.0007725559,0.0010256866,0.004327301],"category_scores_gemma":[0.0006422076,0.00016567062,0.00046068712,0.00051273295,0.0008970893,0.0002617727,0.00042382878,0.0006546452,0.0005516862],"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":[0.00054713467,0.00033135858,0.07937449,0.00029085134,0.000107048356,0.6064579,0.001454107,0.0012038111,0.27883425,0.0022054997,0.0025899294,0.026603684],"study_design_scores_gemma":[0.00019537575,0.00041837423,0.14911482,0.00009694759,0.00021471994,0.8068003,0.00048520573,0.0019186004,0.029782895,0.0006294446,0.010270866,0.00007237671],"about_ca_topic_score_codex":0.049203325,"about_ca_topic_score_gemma":0.051948223,"teacher_disagreement_score":0.049203325,"about_ca_system_score_codex":0.001237915,"about_ca_system_score_gemma":0.0019574026,"threshold_uncertainty_score":0.09783387},"labels":[],"label_agreement":null},{"id":"W2160540953","doi":"10.1136/jmedgenet-2013-102012","title":"<i>KIF1C</i> mutations in two families with hereditary spastic paraparesis and cerebellar dysfunction","year":2013,"lang":"en","type":"article","venue":"Journal of Medical Genetics","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":83,"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 Nautical Research Society","funders":"","keywords":"Missense mutation; Hereditary spastic paraplegia; Genetics; Nonsense mutation; Disease gene identification; Cerebellar ataxia; Exome sequencing; Biology; Mutation; Locus (genetics); Ataxia; Gene; Phenotype; Neuroscience","score_opus":0.019182583094250364,"score_gpt":0.2618280780666484,"score_spread":0.242645494972398,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2160540953","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":[0.99750155,0.0004454829,0.00023914555,0.0001624803,0.00003261276,0.000041887193,0.00011838913,0.000022660088,0.0014357733],"genre_scores_gemma":[0.99868745,0.00013978158,0.00037263802,0.00018376097,0.00002868073,0.00001384882,0.00009517125,0.000012969651,0.00046569918],"study_design_codex":"case_report","study_design_gemma":"observational","domain_scores_codex":[0.9993771,0.0000693173,0.00007312908,0.00017834928,0.00011195703,0.00019021335],"domain_scores_gemma":[0.99926716,0.00014561687,0.00020934021,0.000036508794,0.00009126403,0.00025012103],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00041580404,0.0025674566,0.0007776205,0.0021924232,0.002318598,0.0007187147,0.0009691475,0.0016865276,0.0026999486],"category_scores_gemma":[0.0016247977,0.0006414482,0.00068294536,0.0010911141,0.0011939455,0.00028596306,0.0015356935,0.0007449119,0.0003611489],"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":[0.00059196306,0.00038554444,0.13291618,0.00012540154,0.00016926763,0.832097,0.0042914106,0.00029516197,0.01773905,0.0007062497,0.0007890854,0.0098935785],"study_design_scores_gemma":[0.00016328761,0.00029892515,0.19701578,0.000102180726,0.0001611959,0.7941969,0.000755994,0.000502056,0.0032943243,0.00024357525,0.0032166059,0.000049130475],"about_ca_topic_score_codex":0.013126219,"about_ca_topic_score_gemma":0.0097164605,"teacher_disagreement_score":0.013126219,"about_ca_system_score_codex":0.0019420108,"about_ca_system_score_gemma":0.00082724745,"threshold_uncertainty_score":0.026099622},"labels":[],"label_agreement":null},{"id":"W2162483032","doi":"10.1212/01.wnl.0000161849.29944.43","title":"Two mutations in the <i>HSN2</i> gene explain the high prevalence of HSAN2 in French Canadians","year":2005,"lang":"en","type":"article","venue":"Neurology","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":43,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":true,"ca_institutions":"Centre Hospitalier de l’Université de Montréal","funders":"","keywords":"Gene; Genetics; Mutation; Biology; Medicine","score_opus":0.022173644876079503,"score_gpt":0.2535822702394886,"score_spread":0.2314086253634091,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2162483032","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":[0.9941241,0.00052317075,0.0005111502,0.0003787721,0.00002948953,0.00003678732,0.0004602364,0.000033801178,0.0039025447],"genre_scores_gemma":[0.9980344,0.00019636395,0.00065918645,0.00011789238,0.000014242883,0.0000071444983,0.00020633808,0.000011598678,0.0007527417],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9994978,0.000035490848,0.00002166766,0.00012158508,0.00014791534,0.00017560976],"domain_scores_gemma":[0.99941134,0.00008226343,0.00011812688,0.00002444922,0.00021775876,0.00014592498],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00040579154,0.0011630175,0.00043916234,0.0019881488,0.003525867,0.00066237006,0.0011349715,0.0012617866,0.005656689],"category_scores_gemma":[0.001243843,0.00025902313,0.0006428779,0.0017215105,0.00100602,0.00021027931,0.0006152762,0.00062033336,0.00040544078],"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":[0.00059400353,0.00008968599,0.9393763,0.00010343431,0.00016111611,0.020963773,0.0019315993,0.0005438644,0.010653316,0.00088962057,0.0027489953,0.021944374],"study_design_scores_gemma":[0.00006811815,0.00013904176,0.95454717,0.00009721343,0.00024190157,0.032086615,0.0020589577,0.0015879755,0.0022365379,0.0003517448,0.0065012956,0.00008348781],"about_ca_topic_score_codex":0.86052704,"about_ca_topic_score_gemma":0.8660117,"teacher_disagreement_score":0.13947296,"about_ca_system_score_codex":0.006292901,"about_ca_system_score_gemma":0.0057877377,"threshold_uncertainty_score":0.28058863},"labels":[],"label_agreement":null},{"id":"W2162589030","doi":"10.1186/1750-1172-9-15","title":"A novel recurrent mutation in ATP1A3 causes CAPOS syndrome","year":2014,"lang":"en","type":"article","venue":"Orphanet Journal of Rare Diseases","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":192,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Simon Fraser University; Canada's Michael Smith Genome Sciences Centre; Pacific Centre for Reproductive Medicine; Child and Family Research Institute; University of British Columbia; BC Children's Hospital","funders":"University of Toronto; Michael Smith Health Research BC; Canadian Institutes of Health Research; Genome Canada; McGill University; Université de Montréal; Genome British Columbia; Rare Disease Foundation; University of Ottawa","keywords":"Proband; Missense mutation; Genetics; Sanger sequencing; Exome sequencing; Dystonia; Mutation; Cerebellar ataxia; Sensorineural hearing loss; Medicine; Hearing loss; Ataxia; Biology; Gene; Audiology; Neuroscience","score_opus":0.029120279556264173,"score_gpt":0.2698963322203603,"score_spread":0.24077605266409613,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2162589030","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":[0.9965796,0.00039241934,0.00096044876,0.00013259273,0.000033414224,0.000027026394,0.0002015768,0.00008922364,0.001583797],"genre_scores_gemma":[0.99854434,0.00014023499,0.0006375005,0.00007631974,0.000037151916,0.0000137793895,0.00019826648,0.000017765282,0.0003347319],"study_design_codex":"case_report","study_design_gemma":"observational","domain_scores_codex":[0.9998011,0.00001720514,0.000018002655,0.000066702734,0.000056431676,0.00004069656],"domain_scores_gemma":[0.9996629,0.00010200094,0.00009314372,0.00001878092,0.00002658355,0.00009663815],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00013866535,0.0013397365,0.00047263337,0.0008339436,0.0007840052,0.00038297512,0.0005217395,0.0014643833,0.0022470003],"category_scores_gemma":[0.0008649139,0.0002649543,0.00044828482,0.0007821527,0.00072261976,0.00019428426,0.0006488118,0.00046899397,0.0004338399],"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":[0.00042145068,0.00012811055,0.050231736,0.00020431323,0.00014575299,0.83117765,0.0008312833,0.00049562985,0.1022484,0.0006554692,0.0013734999,0.012086782],"study_design_scores_gemma":[0.00014402198,0.00037256398,0.09439192,0.000057787922,0.00017070558,0.87418604,0.00026971512,0.0015464106,0.023642229,0.0006529806,0.0045224125,0.00004321467],"about_ca_topic_score_codex":0.0015647903,"about_ca_topic_score_gemma":0.0019576708,"teacher_disagreement_score":0.0022470003,"about_ca_system_score_codex":0.0004651397,"about_ca_system_score_gemma":0.0003696816,"threshold_uncertainty_score":0.00751698},"labels":[],"label_agreement":null},{"id":"W2163353660","doi":"10.1016/j.nmd.2015.07.001","title":"Absence of Dystrophin Related Protein-2 disrupts Cajal bands in a patient with Charcot–Marie–Tooth disease","year":2015,"lang":"en","type":"article","venue":"Neuromuscular Disorders","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":30,"is_retracted":false,"has_abstract":false,"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; Canadian Institutes of Health Research; National Institutes of Health; Muscular Dystrophy Association; Wellcome Trust; National Institute of Neurological Disorders and Stroke; Wellcome; Charcot-Marie-Tooth Association","keywords":"Pathology; Dystroglycan; Dystrophin; Exome sequencing; Exome; Skin biopsy; Biology; Medicine; Nerve biopsy; Biopsy; Mutation; Genetics; Muscular dystrophy; Gene; Laminin; Peripheral neuropathy; Extracellular matrix; Endocrinology","score_opus":0.01660486332994434,"score_gpt":0.2214536683079705,"score_spread":0.20484880497802616,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2163353660","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":[0.9930276,0.000662047,0.0009820842,0.0010001122,0.00016856642,0.000046696892,0.00016369132,0.000117122436,0.003831974],"genre_scores_gemma":[0.9981761,0.00015329928,0.0006972333,0.00022458402,0.00010732216,0.000007943605,0.000036390345,0.000034746638,0.0005624287],"study_design_codex":"case_report","study_design_gemma":"case_report","domain_scores_codex":[0.999164,0.00006776069,0.00012822727,0.00026469285,0.00018859301,0.00018672178],"domain_scores_gemma":[0.99824405,0.00074917433,0.00035746204,0.00007506228,0.00011757544,0.0004566231],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00041473616,0.0028763576,0.00092187454,0.003185306,0.0027803194,0.0009991922,0.0017353072,0.0039655254,0.002248828],"category_scores_gemma":[0.003124287,0.00097551214,0.00090684654,0.0014004955,0.002497608,0.0008171102,0.0012585183,0.001972932,0.0004906354],"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":[0.00013853957,0.00006355586,0.0061696586,0.000031828717,0.000029791214,0.97864974,0.00038770383,0.00012764239,0.013037013,0.00021654367,0.00020085774,0.00094712095],"study_design_scores_gemma":[0.000051976003,0.0001265774,0.02224641,0.000021618835,0.00013272563,0.97025573,0.00026019025,0.00084913615,0.005088672,0.00022617732,0.00069948164,0.00004121797],"about_ca_topic_score_codex":0.0059367623,"about_ca_topic_score_gemma":0.0050681285,"teacher_disagreement_score":0.0059367623,"about_ca_system_score_codex":0.0009959447,"about_ca_system_score_gemma":0.00092213583,"threshold_uncertainty_score":0.011804402},"labels":[],"label_agreement":null},{"id":"W2163585832","doi":"10.1016/j.clinph.2006.07.107","title":"BS23 Motor neurone diseases","year":2006,"lang":"en","type":"article","venue":"Clinical Neurophysiology","topic":"Hereditary Neurological Disorders","field":"Neuroscience","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":"University of British Columbia","funders":"","keywords":"Motor neurone disease; Neuroscience; Medicine; Physical medicine and rehabilitation; Amyotrophic lateral sclerosis; Psychology; Internal medicine; Disease","score_opus":0.05515713086875071,"score_gpt":0.327649981741275,"score_spread":0.2724928508725243,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2163585832","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":[0.72870386,0.02267779,0.0060039167,0.0036091139,0.001178036,0.00019037393,0.0054718046,0.0008316096,0.2313335],"genre_scores_gemma":[0.95427907,0.0034451485,0.0015520372,0.0006805597,0.00036330454,0.00006473399,0.0016811999,0.00011787368,0.037816133],"study_design_codex":"case_report","study_design_gemma":"observational","domain_scores_codex":[0.9997534,0.00003093289,0.000029336288,0.00004878355,0.00007171545,0.000065812994],"domain_scores_gemma":[0.9995877,0.0000931066,0.00007111212,0.00003905801,0.00010790105,0.0001009993],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00029009557,0.0014993658,0.00063959364,0.001394227,0.001309925,0.0009340904,0.00082705636,0.0012913665,0.03711287],"category_scores_gemma":[0.0013105427,0.000166092,0.00031109355,0.0010707205,0.00082549074,0.00069941283,0.00086200837,0.00063596695,0.005695266],"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":[0.0020465876,0.00027884828,0.06894822,0.0010506175,0.0003987759,0.5941708,0.0012722315,0.0009954226,0.0771277,0.018360127,0.04543398,0.18991669],"study_design_scores_gemma":[0.00017857751,0.00046409442,0.132136,0.00043640457,0.00038881498,0.67966425,0.0008060458,0.001347495,0.03537071,0.010301213,0.13880233,0.000104095016],"about_ca_topic_score_codex":0.0060332245,"about_ca_topic_score_gemma":0.004878537,"teacher_disagreement_score":0.03711287,"about_ca_system_score_codex":0.0007925863,"about_ca_system_score_gemma":0.00065893977,"threshold_uncertainty_score":0.124154866},"labels":[],"label_agreement":null},{"id":"W2166245090","doi":"10.1371/journal.pone.0063815","title":"Targeted ANP32E Mutant Mice Do Not Demonstrate Obvious Movement Defects","year":2013,"lang":"en","type":"article","venue":"PLoS ONE","topic":"Hereditary Neurological Disorders","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":false,"ca_institutions":"University Health Network","funders":"Duke-NUS Medical School; National Cancer Centre of Singapore","keywords":"Phenotype; Biology; Mutant; Loss function; Genetics; Gene; Mutation; Allele; Function (biology); Gene targeting; Gene knockin; Cell biology","score_opus":0.05206679753344817,"score_gpt":0.21776499964240495,"score_spread":0.16569820210895678,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2166245090","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":[0.9773372,0.00067980133,0.015088698,0.0002197524,0.00008614791,0.00014016846,0.0021677762,0.00051276037,0.0037678475],"genre_scores_gemma":[0.9569942,0.0011204837,0.01747204,0.00019733749,0.0000221351,0.0004744397,0.0034957947,0.00061192,0.019611726],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99955696,0.000033175576,0.000064638545,0.00017582027,0.000120103854,0.00004935129],"domain_scores_gemma":[0.99907,0.00021738751,0.00027524235,0.00012203513,0.0000712137,0.00024417514],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00030473238,0.0010326309,0.00044950435,0.0010377814,0.00030522846,0.00037524017,0.0007556047,0.0009293601,0.007858365],"category_scores_gemma":[0.0004206564,0.00032429918,0.00031634883,0.00023693462,0.00089558016,0.00042552687,0.00067952974,0.0013207714,0.0018605315],"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":[0.00012071084,0.00004687009,0.00026357124,0.000041499345,0.000010303378,0.00017487077,0.000025789946,0.000033885313,0.99814713,0.00016274973,0.00005710466,0.0009155236],"study_design_scores_gemma":[0.00007056755,0.00044231294,0.0079334425,0.000035991918,0.000059026992,0.003592431,0.000063752705,0.00074044766,0.9823663,0.0002723099,0.0044064843,0.000016906679],"about_ca_topic_score_codex":0.0004443562,"about_ca_topic_score_gemma":0.0009220101,"teacher_disagreement_score":0.007858365,"about_ca_system_score_codex":0.00028155372,"about_ca_system_score_gemma":0.00027261453,"threshold_uncertainty_score":0.026288867},"labels":[],"label_agreement":null},{"id":"W2166367631","doi":"10.1242/dmm.002527","title":"An ENU-induced mutation in mouse glycyl-tRNA synthetase (GARS) causes peripheral sensory and motor phenotypes creating a model of Charcot-Marie-Tooth type 2D peripheral neuropathy","year":2009,"lang":"en","type":"article","venue":"Disease Models & Mechanisms","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":102,"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 Calgary","funders":"National Institute of Neurological Disorders and Stroke; Wellcome Trust","keywords":"Biology; Mutation; Phenotype; Heterozygote advantage; Axon; Congenic; Peripheral nervous system; Loss function; Peripheral neuropathy; Atrophy; Genetics; Mutant; Internal medicine; Endocrinology; Central nervous system; Neuroscience; Gene; Allele; Medicine","score_opus":0.042054956404196014,"score_gpt":0.2666708646053253,"score_spread":0.22461590820112928,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2166367631","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":[0.98900884,0.00088752847,0.0067049228,0.00020227215,0.00010584217,0.00018837409,0.00055283227,0.00033436582,0.0020149923],"genre_scores_gemma":[0.9619797,0.002308852,0.019546738,0.00015204513,0.00007020931,0.00036823604,0.0015956464,0.00017558264,0.013802948],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99942017,0.000114925395,0.00009346247,0.00013282301,0.00015960698,0.000079064324],"domain_scores_gemma":[0.9995871,0.000050645493,0.00011042387,0.000058726153,0.00002639005,0.00016677022],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00039818822,0.0015254166,0.0005194096,0.0015761977,0.00051671785,0.0003846806,0.00069444743,0.0010617388,0.0024292355],"category_scores_gemma":[0.00020550695,0.0005199059,0.000658694,0.00038526373,0.0007651658,0.00045341926,0.00088748574,0.0011662735,0.000871357],"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":[0.00023158392,0.00017842182,0.00023389871,0.000049079437,0.000011161535,0.00056079455,0.000045895857,0.000101023434,0.9968418,0.00032014737,0.000070306865,0.0013559029],"study_design_scores_gemma":[0.00026809762,0.002971229,0.008284492,0.00006199412,0.00009242719,0.007807334,0.00012544649,0.002122228,0.9646372,0.0003566481,0.013227752,0.00004509024],"about_ca_topic_score_codex":0.00045698168,"about_ca_topic_score_gemma":0.0009050373,"teacher_disagreement_score":0.0024292355,"about_ca_system_score_codex":0.00038245885,"about_ca_system_score_gemma":0.000318921,"threshold_uncertainty_score":0.0081266165},"labels":[],"label_agreement":null},{"id":"W2167623783","doi":"10.1186/s12883-015-0481-3","title":"Adult-onset autosomal dominant spastic paraplegia linked to a GTPase-effector domain mutation of dynamin 2","year":2015,"lang":"en","type":"article","venue":"BMC Neurology","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":51,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Queen's University; Kingston General Hospital","funders":"National Institute of Neurological Disorders and Stroke; National Human Genome Research Institute; Uniformed Services University of the Health Sciences; National Institutes of Health; Ministry of Education and Science of the Russian Federation","keywords":"Missense mutation; Biology; Genetics; Mutation; Dynamin; Exome sequencing; Disease gene identification; Hereditary spastic paraplegia; Neuroscience; Phenotype; Gene; Endocytosis","score_opus":0.0377771779337342,"score_gpt":0.28066647905316466,"score_spread":0.24288930111943047,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2167623783","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":[0.997912,0.00017657102,0.0007988279,0.00006494626,0.000019378122,0.000020204205,0.0002043119,0.000039713996,0.0007639411],"genre_scores_gemma":[0.9987086,0.0000762279,0.00047048833,0.000061639825,0.000016722912,0.0000066240614,0.00017435483,0.0000050266726,0.00048042674],"study_design_codex":"case_report","study_design_gemma":"observational","domain_scores_codex":[0.9999232,0.000009250946,0.000012852466,0.000022480197,0.000018754932,0.000013397526],"domain_scores_gemma":[0.9998235,0.000047736376,0.0000583918,0.000008641513,0.000018055278,0.000043741074],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00015700706,0.0009307217,0.00032281177,0.00042300115,0.00051128253,0.00017145558,0.00021175912,0.0005273291,0.0019542342],"category_scores_gemma":[0.0003277458,0.00014046792,0.00028678816,0.00035806643,0.00034338428,0.00010015106,0.00037726818,0.00040150993,0.0003440444],"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":[0.00076658936,0.0003969433,0.13234228,0.0003216572,0.00024797153,0.5550842,0.0010420843,0.0010688079,0.29416898,0.00079838367,0.001463947,0.012298183],"study_design_scores_gemma":[0.00012531526,0.00061793526,0.32129616,0.000057660058,0.00023049566,0.6435422,0.00022970358,0.0027133126,0.027191766,0.00039383926,0.0035652916,0.000036374728],"about_ca_topic_score_codex":0.0009731427,"about_ca_topic_score_gemma":0.0010974951,"teacher_disagreement_score":0.0019542342,"about_ca_system_score_codex":0.0002546993,"about_ca_system_score_gemma":0.00021917793,"threshold_uncertainty_score":0.0065375566},"labels":[],"label_agreement":null},{"id":"W2169889176","doi":"10.1002/ana.20590","title":"New locus for hereditary spastic paraplegia maps to chromosome 1p31.1-1p21.1","year":2005,"lang":"en","type":"article","venue":"Annals of Neurology","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":31,"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 Health Network; Toronto Western Hospital; Occupational Cancer Research Centre; University of Toronto","funders":"","keywords":"Sorting nexin; Hereditary spastic paraplegia; Locus (genetics); Spastic; Paraplegia; Genetics; Medicine; Biology; Gene; Neuroscience; Phenotype; Spinal cord; Physical medicine and rehabilitation; Cerebral palsy","score_opus":0.09397576350102776,"score_gpt":0.3301815393186701,"score_spread":0.23620577581764235,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2169889176","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":[0.97237724,0.005862084,0.008952791,0.0023475098,0.00046381596,0.00012107512,0.001198331,0.00048473617,0.008192424],"genre_scores_gemma":[0.9834379,0.0021436738,0.0064739916,0.00050362933,0.00040768093,0.00006832535,0.0021064267,0.000028798673,0.004829595],"study_design_codex":"case_report","study_design_gemma":"observational","domain_scores_codex":[0.99979645,0.000034419627,0.00002180088,0.000044577362,0.00007174296,0.000031056272],"domain_scores_gemma":[0.99963236,0.00010935529,0.000082123894,0.00002304653,0.00007206379,0.00008099925],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00034045955,0.0011095717,0.0007362994,0.0011003095,0.0006532575,0.00046574685,0.00065509917,0.0007021102,0.0033903471],"category_scores_gemma":[0.00088169525,0.00018246975,0.0005178647,0.0006394534,0.00044772108,0.00024814182,0.00059762294,0.0007213362,0.0006489231],"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":[0.0017429455,0.0005716744,0.11946625,0.0006973281,0.00060585875,0.40782955,0.0025768674,0.0016368314,0.24382183,0.0049825558,0.019007657,0.19706066],"study_design_scores_gemma":[0.0005853866,0.0014540877,0.4065223,0.00024739868,0.0006904068,0.47236893,0.00041102493,0.0029357055,0.023906095,0.004753204,0.085944116,0.00018135001],"about_ca_topic_score_codex":0.0023687254,"about_ca_topic_score_gemma":0.0043362407,"teacher_disagreement_score":0.0033903471,"about_ca_system_score_codex":0.0005395501,"about_ca_system_score_gemma":0.00043276945,"threshold_uncertainty_score":0.01134181},"labels":[],"label_agreement":null},{"id":"W2169985154","doi":"10.1017/s0317167100012774","title":"CYP7B1 Mutations in French-Canadian Hereditary Spastic Paraplegia Subjects","year":2012,"lang":"en","type":"article","venue":"Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":5,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":true,"route_about_ca":true,"ca_institutions":"Centre Hospitalier Universitaire Sainte-Justine; Université Laval; Université de Montréal; Centre Hospitalier de l’Université de Montréal","funders":"Canadian Institutes of Health Research","keywords":"Hereditary spastic paraplegia; Paraplegia; Spastic; Medicine; Physical medicine and rehabilitation; Action (physics); Neuroscience; Psychology; Genetics; Biology; Spinal cord; Phenotype; Gene; Cerebral palsy; Physics","score_opus":0.05027662154929395,"score_gpt":0.27254254972811925,"score_spread":0.2222659281788253,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2169985154","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":[0.9875711,0.0013571164,0.00017448919,0.00045571214,0.000056900546,0.000047534795,0.0029202204,0.00002831538,0.007388633],"genre_scores_gemma":[0.9963373,0.0005196199,0.00017453838,0.00010389058,0.000025733194,0.000010323453,0.0007383847,0.000010192405,0.0020801055],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9996785,0.000020261527,0.000025301077,0.00008476427,0.000092523565,0.00009877773],"domain_scores_gemma":[0.99955744,0.00008711877,0.00009441172,0.000016949767,0.00011349866,0.0001305699],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0002561024,0.0010305532,0.00044819765,0.0021011543,0.0019967451,0.00069680315,0.00054406386,0.0009754944,0.009409869],"category_scores_gemma":[0.0010213436,0.00025190198,0.0005292443,0.0021031857,0.0006542079,0.00018701225,0.00031173753,0.0004381602,0.00063280686],"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":[0.0028914334,0.00029324857,0.8840108,0.00023050165,0.00037544323,0.046429466,0.0027662676,0.0009094751,0.013113288,0.0016456557,0.012784683,0.034549776],"study_design_scores_gemma":[0.00009860855,0.00016728687,0.9732108,0.00010811992,0.00024184535,0.01867232,0.0010624545,0.00063028844,0.0009320067,0.00019268523,0.0046385196,0.000045075256],"about_ca_topic_score_codex":0.78423685,"about_ca_topic_score_gemma":0.7467554,"teacher_disagreement_score":0.21576315,"about_ca_system_score_codex":0.003622346,"about_ca_system_score_gemma":0.0027913554,"threshold_uncertainty_score":0.4340676},"labels":[],"label_agreement":null},{"id":"W2170208995","doi":"10.1111/cge.12030","title":"<i><scp>HINT1</scp></i> mutations define a novel disease entity – autosomal recessive axonal neuropathy with neuromyotonia","year":2012,"lang":"en","type":"letter","venue":"Clinical Genetics","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":10,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of British Columbia; Centre for Drug Research and Development","funders":"","keywords":"Neuromyotonia; Genetics; Mutation; Medicine; Disease; Neuroscience; Biology; Gene; Pathology; Antibody","score_opus":0.0868404495587412,"score_gpt":0.3138475768617447,"score_spread":0.2270071273030035,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2170208995","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":[0.07828384,0.009460559,0.0023312548,0.8356447,0.0206909,0.00015716314,0.0006208038,0.00043372475,0.052377053],"genre_scores_gemma":[0.6133912,0.008916961,0.0036434687,0.26047355,0.083841115,0.00015111663,0.00045324847,0.00013694537,0.028992437],"study_design_codex":"case_report","study_design_gemma":"case_report","domain_scores_codex":[0.9996408,0.00007915489,0.000048460763,0.00005634826,0.00008104846,0.000094154326],"domain_scores_gemma":[0.99913967,0.000382114,0.000081579274,0.000047533016,0.00019262185,0.0001565067],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00041418895,0.0009212984,0.0008786182,0.00061481056,0.0010648496,0.0010625832,0.000918748,0.012288475,0.0031241446],"category_scores_gemma":[0.0031211697,0.0004056857,0.00065627747,0.00041969973,0.001485276,0.0011383671,0.00043629177,0.0053911167,0.002414679],"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":[0.0005865214,0.0001208972,0.015076193,0.00021604713,0.000082994025,0.5577544,0.00028904015,0.00054270076,0.005662117,0.0047072507,0.39010203,0.02485989],"study_design_scores_gemma":[0.00055935193,0.00029120885,0.031794198,0.00029029493,0.00019318891,0.7831726,0.0004665965,0.0056613083,0.0043024216,0.013244255,0.15986548,0.00015910105],"about_ca_topic_score_codex":0.003653658,"about_ca_topic_score_gemma":0.0038569574,"teacher_disagreement_score":0.012288475,"about_ca_system_score_codex":0.0016275817,"about_ca_system_score_gemma":0.0005312873,"threshold_uncertainty_score":0.011808991},"labels":[],"label_agreement":null},{"id":"W2171005559","doi":"10.1016/j.nmd.2015.07.017","title":"Autosomal recessive axonal polyneuropathy in a sibling pair due to a novel homozygous mutation in IGHMBP2","year":2015,"lang":"en","type":"article","venue":"Neuromuscular Disorders","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":29,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Ottawa; McGill University; Children's Hospital of Eastern Ontario","funders":"Fonds de Recherche du Québec - Santé; Genome Canada; Canadian Institutes of Health Research; Children's Hospital of Eastern Ontario Foundation; National Heart, Lung, and Blood Institute; Génome Québec; Ontario Genomics Institute","keywords":"Exome sequencing; Spinal muscular atrophy; Mutation; Medicine; Phenotype; Respiratory distress; Compound heterozygosity; Genetics; Biology; Gene; Bioinformatics","score_opus":0.04135092477231674,"score_gpt":0.2680255629860156,"score_spread":0.22667463821369885,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2171005559","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":[0.97843665,0.0011300029,0.0028493262,0.002478214,0.0007870521,0.00019133302,0.00086285354,0.0002365998,0.01302791],"genre_scores_gemma":[0.9936727,0.0002802695,0.001286207,0.000491255,0.00027976136,0.00003983412,0.00017781288,0.000050876853,0.0037212756],"study_design_codex":"case_report","study_design_gemma":"observational","domain_scores_codex":[0.9993605,0.00006157825,0.00006587954,0.0002166172,0.00015303785,0.00014229113],"domain_scores_gemma":[0.99910706,0.00025073887,0.00015596491,0.00005015873,0.00009124279,0.00034482486],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0003782661,0.0034638627,0.0012530109,0.0017129416,0.0028695317,0.000955894,0.0018702681,0.004065774,0.007529194],"category_scores_gemma":[0.0021436359,0.00079522363,0.0011850479,0.0010177362,0.0015473937,0.00089524104,0.0015927244,0.0018954653,0.0014485739],"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":[0.00005908334,0.00004459198,0.0030929968,0.000024195757,0.000021743343,0.990969,0.0001785175,0.00005561286,0.0044510914,0.00019192322,0.000298834,0.00061239034],"study_design_scores_gemma":[0.000055679226,0.00014239817,0.0125467535,0.00002302894,0.000082575265,0.9825744,0.00026271638,0.0005260477,0.0025227244,0.00025945713,0.0009778227,0.000026390251],"about_ca_topic_score_codex":0.0043424354,"about_ca_topic_score_gemma":0.0035083948,"teacher_disagreement_score":0.007529194,"about_ca_system_score_codex":0.0011475114,"about_ca_system_score_gemma":0.0009595929,"threshold_uncertainty_score":0.025187671},"labels":[],"label_agreement":null},{"id":"W2171397001","doi":"10.1093/hmg/ddq149","title":"Reversal of neuropathy phenotypes in conditional mouse model of Charcot–Marie–Tooth disease type 2E","year":2010,"lang":"en","type":"article","venue":"Human Molecular Genetics","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":54,"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 Laval","funders":"Canadian Institutes of Health Research","keywords":"Biology; Phenotype; Tooth disease; Genetics; Disease; Gene; Internal medicine","score_opus":0.03231862778091286,"score_gpt":0.2637323371132841,"score_spread":0.23141370933237124,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2171397001","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":[0.9930748,0.0008297191,0.0025809023,0.00024062504,0.0000974861,0.0001330009,0.00071669585,0.00034190554,0.001984946],"genre_scores_gemma":[0.9820661,0.0012618462,0.004832672,0.00017095254,0.00004110353,0.00031797972,0.0012401744,0.000118918295,0.009950225],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99967,0.00005661471,0.00003984771,0.00008713332,0.00008151943,0.00006490048],"domain_scores_gemma":[0.9997336,0.00004284826,0.00008757131,0.00003288788,0.00001666157,0.00008633582],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00037794604,0.0010105338,0.0004471935,0.0007155208,0.00032560623,0.00032096374,0.0005304865,0.0009457898,0.0020943885],"category_scores_gemma":[0.00025547415,0.00039112443,0.0004254646,0.00021056902,0.00072208693,0.00039307427,0.0003941074,0.0012900234,0.00059570646],"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":[0.00029463987,0.00028056448,0.00022494038,0.00007270321,0.000015235411,0.00058356195,0.000047817903,0.0001383322,0.99621755,0.00043568647,0.00015519946,0.001533781],"study_design_scores_gemma":[0.000447913,0.0027813462,0.00713668,0.00006017119,0.00006838803,0.003964325,0.00009521324,0.0027357703,0.9738012,0.00030269817,0.008568338,0.00003795974],"about_ca_topic_score_codex":0.0009278676,"about_ca_topic_score_gemma":0.0019449302,"teacher_disagreement_score":0.0020943885,"about_ca_system_score_codex":0.00048876944,"about_ca_system_score_gemma":0.00040958682,"threshold_uncertainty_score":0.007006407},"labels":[],"label_agreement":null},{"id":"W2173584202","doi":"10.1093/brain/awv320","title":"ALS5/SPG11/<i>KIAA1840</i>mutations cause autosomal recessive axonal Charcot–Marie–Tooth disease","year":2015,"lang":"en","type":"article","venue":"Brain","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":100,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":true,"ca_institutions":"Occupational Cancer Research Centre; University of Toronto","funders":"Medical Research Council; Ministero della Salute; Canada Excellence Research Chairs, Government of Canada; Japan Society for the Promotion of Science; Brain Science Foundation; Wellcome Trust","keywords":"Tooth disease; Genetics; Medicine; Disease; Biology; Pathology","score_opus":0.08080019355768839,"score_gpt":0.3055887007680509,"score_spread":0.2247885072103625,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2173584202","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":[0.9982345,0.00028866553,0.00037136505,0.000017991786,0.00000498755,0.000024710625,0.00024477055,0.000017877976,0.00079501484],"genre_scores_gemma":[0.99851996,0.0001915114,0.00045211197,0.0000487979,0.000005832243,0.0000110167675,0.0003591957,0.0000076100673,0.00040399327],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.99977666,0.000022455306,0.000027041206,0.00006727998,0.00006471017,0.000041876807],"domain_scores_gemma":[0.9998178,0.000040377716,0.00005378705,0.000009757263,0.00001977087,0.000058529065],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0001551382,0.0008429174,0.00027146892,0.0007939958,0.00050845207,0.00020958012,0.0002634269,0.00047574413,0.0015891221],"category_scores_gemma":[0.00043075602,0.00021133859,0.00028164365,0.00052740425,0.00044561262,0.00013191086,0.0005284756,0.00024564826,0.00044474524],"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":[0.0007998226,0.00029416548,0.34688115,0.00026770143,0.0002724721,0.11352911,0.0018849353,0.0006776183,0.51057285,0.000421694,0.0009338032,0.023464702],"study_design_scores_gemma":[0.000083764164,0.0007140063,0.8822186,0.00004802177,0.00014245936,0.07958879,0.0006701765,0.0006012376,0.030636108,0.00021788415,0.00504438,0.000034535617],"about_ca_topic_score_codex":0.0026095307,"about_ca_topic_score_gemma":0.0024876464,"teacher_disagreement_score":0.0026095307,"about_ca_system_score_codex":0.00024663768,"about_ca_system_score_gemma":0.00015226385,"threshold_uncertainty_score":0.0053161383},"labels":[],"label_agreement":null},{"id":"W2182706109","doi":"10.1038/ejhg.2015.240","title":"SPG7 mutations explain a significant proportion of French Canadian spastic ataxia cases","year":2015,"lang":"en","type":"article","venue":"European Journal of Human Genetics","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":59,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":true,"ca_institutions":"Hôpital Fleurimont; Centre Hospitalier Universitaire de Sherbrooke; Université Laval; Cégep de Jonquière; Université de Sherbrooke; McGill University and Génome Québec Innovation Centre; Children's Hospital of Eastern Ontario; McGill University; Hôpital de l'Enfant-Jésus; University of Ottawa; Montreal Neurological Institute and Hospital","funders":"","keywords":"Ataxia; Hereditary spastic paraplegia; Cerebellar ataxia; Genetics; Medicine; Spastic; Sanger sequencing; Cohort; Mutation; Exome sequencing; Spasticity; Compound heterozygosity; Biology; Gene; Internal medicine; Phenotype; Physical therapy; Cerebral palsy; Psychiatry","score_opus":0.10992025678166804,"score_gpt":0.2832299297824416,"score_spread":0.17330967300077355,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2182706109","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":[0.94726956,0.008466032,0.0023523597,0.002428922,0.00024283164,0.00009512726,0.0066328766,0.00030992806,0.032202467],"genre_scores_gemma":[0.98759764,0.002919096,0.0013059288,0.00035606866,0.00010437477,0.000025705247,0.0020459513,0.000084163294,0.0055610454],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9991418,0.00007479087,0.000057101464,0.0001920696,0.0003142897,0.00021995806],"domain_scores_gemma":[0.9993316,0.00014810685,0.00012248712,0.000042924425,0.0002632295,0.00009165667],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0005736338,0.0019318351,0.0008191348,0.0044192593,0.0024812345,0.0011778263,0.0010544836,0.0014646671,0.012213665],"category_scores_gemma":[0.0020447683,0.00036115976,0.0010563114,0.0038361938,0.0011374669,0.00041574694,0.0008670697,0.0005510663,0.0012896108],"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":[0.001241786,0.00013429219,0.67182976,0.00070220354,0.0010281365,0.08567036,0.0036564907,0.0018626277,0.03282096,0.0065719616,0.034554042,0.15992741],"study_design_scores_gemma":[0.00011238186,0.00013050156,0.8483078,0.00036915013,0.0008714633,0.09485555,0.0026241015,0.0013735102,0.0034429193,0.0018704631,0.045926206,0.000115826784],"about_ca_topic_score_codex":0.58078766,"about_ca_topic_score_gemma":0.62760675,"teacher_disagreement_score":0.41921234,"about_ca_system_score_codex":0.0033151533,"about_ca_system_score_gemma":0.0055153724,"threshold_uncertainty_score":0.84336233},"labels":[],"label_agreement":null},{"id":"W2188620495","doi":"10.1007/s12098-016-2052-z","title":"Imaging in Pediatric Demyelinating and Inflammatory Diseases of Brain- Part 2","year":2016,"lang":"en","type":"review","venue":"The Indian Journal of Pediatrics","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":4,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Hospital for Sick Children","funders":"","keywords":"Medicine; Demyelinating Disorder; Neuroimaging; Multiple sclerosis; Susceptibility weighted imaging; Magnetic resonance imaging; Pediatrics; Pathology; Radiology; Immunology; Psychiatry","score_opus":0.03039585842050138,"score_gpt":0.29454743007566553,"score_spread":0.2641515716551641,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2188620495","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":[0.00026033644,0.9983712,0.00017360417,0.00021788155,0.00013057275,0.0000039902857,0.000019706355,0.000007634002,0.0008150495],"genre_scores_gemma":[0.0030239215,0.99518716,0.0005643769,0.00025696543,0.0005358521,0.0000070499327,0.00004785691,0.000003776214,0.0003730462],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.9997104,0.000053879732,0.000080747566,0.000052923642,0.000070644805,0.000031260675],"domain_scores_gemma":[0.99918383,0.0004303778,0.000165411,0.00001956175,0.00014061348,0.000060089278],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0005622491,0.0010175791,0.0013653049,0.0050259647,0.00025407402,0.0011380352,0.0011244778,0.0012473839,0.0020176808],"category_scores_gemma":[0.0014176908,0.00036986262,0.00057393545,0.003375098,0.0008215702,0.0015263981,0.0006906616,0.0015767006,0.0010235348],"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":[0.00008191969,0.000082107166,0.0025442918,0.017217236,0.00014735156,0.0061308984,0.000151368,0.0006954473,0.0022182215,0.0024784314,0.0350626,0.93319017],"study_design_scores_gemma":[0.000047546004,0.00012519884,0.01027755,0.015439626,0.0006539756,0.10987144,0.00038556347,0.00052440126,0.0018635503,0.0039316616,0.856778,0.00010158898],"about_ca_topic_score_codex":0.002166095,"about_ca_topic_score_gemma":0.0029605478,"teacher_disagreement_score":0.0050259647,"about_ca_system_score_codex":0.00067127944,"about_ca_system_score_gemma":0.0012090752,"threshold_uncertainty_score":0.006749809},"labels":[],"label_agreement":null},{"id":"W2197024822","doi":"10.1212/wnl.0000000000002241","title":"Clinical Reasoning: A 64-year-old man with progressive paraspinal muscle weakness","year":2015,"lang":"en","type":"article","venue":"Neurology","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":7,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University Health Network","funders":"","keywords":"Weakness; Dysphagia; Medicine; Physical medicine and rehabilitation; Ptosis; Muscle weakness; Physical therapy; Facial weakness; Stairs; Pediatrics; Surgery; Internal medicine","score_opus":0.07642623273638764,"score_gpt":0.33726490179156393,"score_spread":0.2608386690551763,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2197024822","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":[0.8924637,0.007249909,0.003960544,0.017384099,0.0015611169,0.00068192603,0.0018563314,0.00048982736,0.074352555],"genre_scores_gemma":[0.98565334,0.0021001734,0.0012026016,0.0031634076,0.0010219115,0.000047449637,0.00047315907,0.00003578201,0.006302155],"study_design_codex":"case_report","study_design_gemma":"case_report","domain_scores_codex":[0.9996997,0.000021367932,0.00003410583,0.00010215404,0.00005119882,0.00009143249],"domain_scores_gemma":[0.9995573,0.00008276289,0.00005516405,0.000021588055,0.000070677794,0.000212539],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00021372038,0.0024518357,0.0011308521,0.0014301308,0.00189758,0.0007826444,0.0011876158,0.004037351,0.005758256],"category_scores_gemma":[0.0016544644,0.0005093468,0.00053590717,0.0010700016,0.00085062685,0.0016415314,0.0007526564,0.0021558355,0.0018069509],"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":[0.000052003285,0.000052277417,0.011774967,0.00004528265,0.000009495444,0.9836469,0.00021500581,0.00011398114,0.00067186245,0.00017670385,0.0017214027,0.0015200232],"study_design_scores_gemma":[0.0000239131,0.00012367661,0.014276945,0.000073746094,0.000016524154,0.9818304,0.0002871246,0.00027052022,0.00021903886,0.0004270582,0.0024335666,0.000017489425],"about_ca_topic_score_codex":0.0035068013,"about_ca_topic_score_gemma":0.00488246,"teacher_disagreement_score":0.005758256,"about_ca_system_score_codex":0.0006706821,"about_ca_system_score_gemma":0.0008018318,"threshold_uncertainty_score":0.019263268},"labels":[],"label_agreement":null},{"id":"W2198619828","doi":"10.1016/j.crad.2015.09.010","title":"A practical approach to diseases affecting dentate nuclei","year":2015,"lang":"en","type":"review","venue":"Clinical Radiology","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":22,"is_retracted":false,"has_abstract":false,"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":"Medicine; Radiological weapon; Fluid-attenuated inversion recovery; Differential diagnosis; Radiology; Clinical Practice; Clinical imaging; Medical physics; Pathology; Magnetic resonance imaging; Physical therapy","score_opus":0.46372662431822237,"score_gpt":0.5269549154936727,"score_spread":0.06322829117545031,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2198619828","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":[0.00010524152,0.99642205,0.000553407,0.0006734889,0.000632868,0.0000072896682,0.000022656686,0.000019324589,0.0015636776],"genre_scores_gemma":[0.0012346075,0.9943198,0.0010908822,0.00089963165,0.0010675751,0.000010775213,0.000064992644,0.000003999098,0.0013076399],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.99980193,0.00003630897,0.000048741225,0.000032858155,0.00006111048,0.000019077783],"domain_scores_gemma":[0.9995426,0.00022354838,0.000059630383,0.000016675012,0.00011469967,0.000042941716],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0005956852,0.001427156,0.0013581429,0.004035752,0.00029629137,0.0010949783,0.00089775847,0.0017091003,0.003471187],"category_scores_gemma":[0.0011647546,0.00035895026,0.00056613545,0.0019231279,0.00078758824,0.0019175884,0.00119348,0.0022022799,0.0018872154],"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":[0.000057617566,0.00004560116,0.0002889565,0.014816677,0.00010220416,0.0015258926,0.000081419785,0.00042863295,0.0016937144,0.004521506,0.063228704,0.9132092],"study_design_scores_gemma":[0.000029079556,0.000055695986,0.00081513915,0.004825988,0.0002014112,0.0073364726,0.00009854041,0.00013403055,0.00038669992,0.003766991,0.9823173,0.00003255948],"about_ca_topic_score_codex":0.0010106802,"about_ca_topic_score_gemma":0.0029205075,"teacher_disagreement_score":0.004035752,"about_ca_system_score_codex":0.0006713524,"about_ca_system_score_gemma":0.0013974028,"threshold_uncertainty_score":0.011612296},"labels":[],"label_agreement":null},{"id":"W2208395593","doi":"10.1017/cjn.2015.162","title":"Novel VCP mutation associated with CMT2 phenotype","year":2015,"lang":"en","type":"article","venue":"Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":0,"is_retracted":false,"has_abstract":true,"route_ca_aff":false,"route_ca_fund":false,"route_ca_venue":true,"route_about_ca":false,"ca_institutions":"","funders":"","keywords":"Proband; Hereditary spastic paraplegia; Amyotrophic lateral sclerosis; Medicine; Phenotype; Exome sequencing; Frontotemporal dementia; Pathology; Mutation; Upper motor neuron; Genetics; Disease; Dementia; Biology; Gene","score_opus":0.08021164441646865,"score_gpt":0.27564006877492475,"score_spread":0.1954284243584561,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2208395593","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":[0.9940897,0.00047947065,0.00093638716,0.0003538188,0.00010455781,0.000061161896,0.00043353677,0.000083548024,0.0034578575],"genre_scores_gemma":[0.9976597,0.00011798046,0.0005558735,0.00012849759,0.00009568885,0.000018795103,0.00033893547,0.000020763395,0.001063677],"study_design_codex":"case_report","study_design_gemma":"observational","domain_scores_codex":[0.99968636,0.00002139187,0.000022994072,0.00012369861,0.000070070244,0.00007551858],"domain_scores_gemma":[0.99951124,0.00013113963,0.00008295354,0.000020197367,0.000053596592,0.00020085627],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00015457135,0.0018698338,0.00055994623,0.0010462612,0.0010058063,0.0006795491,0.0006472129,0.0026215792,0.004278499],"category_scores_gemma":[0.00097412645,0.0002955973,0.00051479856,0.0008486288,0.00065315695,0.0003583936,0.00088430673,0.0009216163,0.00081207516],"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":[0.000114694245,0.00007415938,0.01051545,0.00007546455,0.00002203728,0.9646609,0.00026910656,0.00023492382,0.020741003,0.0002591237,0.0008352317,0.0021979355],"study_design_scores_gemma":[0.000052525716,0.0001278816,0.01637502,0.000023551811,0.000020469995,0.9768215,0.0000792624,0.00071516633,0.004334271,0.0001638616,0.0012662718,0.000020265248],"about_ca_topic_score_codex":0.001415339,"about_ca_topic_score_gemma":0.0012058935,"teacher_disagreement_score":0.004278499,"about_ca_system_score_codex":0.00059156114,"about_ca_system_score_gemma":0.0004321437,"threshold_uncertainty_score":0.014313042},"labels":[],"label_agreement":null},{"id":"W2224019944","doi":"","title":"Understanding the pathogenic mechanisms underlying the X-linked Charcot-Marie-Tooth neuropathy (CMTX6) caused by the R158H PDK3 mutation","year":2015,"lang":"en","type":"article","venue":"Journal of the Peripheral Nervous System","topic":"Hereditary Neurological Disorders","field":"Neuroscience","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":"Royal Ottawa Mental Health Centre","funders":"","keywords":"Tooth disease; Mutation; Medicine; Genetics; Biology; Gene","score_opus":0.14686546556775057,"score_gpt":0.27433720708027914,"score_spread":0.12747174151252857,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2224019944","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":[0.8726905,0.07797111,0.020418338,0.015815783,0.0005421105,0.000072529154,0.00036704197,0.00024247017,0.011880275],"genre_scores_gemma":[0.9525863,0.034574427,0.008253229,0.0014033184,0.00027599686,0.00003234104,0.00025346928,0.000018545632,0.0026024715],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99985564,0.000017841858,0.00001851216,0.00003643323,0.000038255468,0.00003333495],"domain_scores_gemma":[0.9998766,0.000022723854,0.000050044408,0.00000871118,0.000018012654,0.00002386175],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00035611156,0.00046193704,0.00039409444,0.00038491152,0.00031970156,0.0008979719,0.0008585398,0.0016689174,0.0011882518],"category_scores_gemma":[0.000378637,0.00021315464,0.00029401155,0.00016201816,0.0007511986,0.0016068867,0.0005486332,0.0013046925,0.0003794419],"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":[0.0013395948,0.00052288815,0.02947124,0.0018374533,0.00019412568,0.025208501,0.0013280665,0.0076123145,0.7457239,0.04075145,0.006873527,0.13913691],"study_design_scores_gemma":[0.0005138201,0.0017092692,0.13782234,0.002299128,0.00073642604,0.12630303,0.006984299,0.052888803,0.3589135,0.1842153,0.1273086,0.00030542808],"about_ca_topic_score_codex":0.001232007,"about_ca_topic_score_gemma":0.0014081863,"teacher_disagreement_score":0.0016689174,"about_ca_system_score_codex":0.00067380315,"about_ca_system_score_gemma":0.00087472313,"threshold_uncertainty_score":0.004888773},"labels":[],"label_agreement":null},{"id":"W2226492912","doi":"10.1093/hmg/ddv632","title":"Conserved pharmacological rescue of hereditary spastic paraplegia-related phenotypes across model organisms","year":2016,"lang":"en","type":"article","venue":"Human Molecular Genetics","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":38,"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; Montreal Neurological Institute and Hospital; Université de Montréal; Women and Children’s Health Research Institute; University of Alberta","funders":"Canadian Institutes of Health Research; National Institutes of Health; Canada Research Chairs","keywords":"Biology; Hereditary spastic paraplegia; Phenotype; Zebrafish; Unfolded protein response; Genetics; Mutation; Gene; Model organism; Loss function","score_opus":0.04912830016099377,"score_gpt":0.30658772606911816,"score_spread":0.2574594259081244,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2226492912","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":[0.9927617,0.0013124882,0.0023553588,0.00018511301,0.000052892767,0.0001316573,0.0009632435,0.00027838143,0.0019591765],"genre_scores_gemma":[0.9881307,0.002058549,0.0048381053,0.000108806365,0.000011222946,0.00017914928,0.0010951813,0.000059788024,0.0035184796],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9998005,0.00003299747,0.00002600019,0.000045904115,0.000055537945,0.00003904859],"domain_scores_gemma":[0.99983823,0.00001644211,0.00005360395,0.000020438607,0.000023793644,0.00004738953],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00016673004,0.0006590491,0.00047404246,0.0006629432,0.0002215431,0.00021991019,0.0004595146,0.00043358703,0.0015946757],"category_scores_gemma":[0.00013794252,0.00015841387,0.00032775206,0.00021538147,0.0003567706,0.00021831678,0.00032627024,0.0008054287,0.00023444855],"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":[0.00010996309,0.00009244662,0.00007478884,0.000048916452,0.000010340786,0.00005786298,0.000011015186,0.00006910033,0.99826896,0.00006680803,0.00004612377,0.0011436006],"study_design_scores_gemma":[0.00005897576,0.002143753,0.0033834311,0.000021183785,0.00003685013,0.00019817855,0.000037276153,0.0005577837,0.99214536,0.000055236786,0.0013537486,0.000008112412],"about_ca_topic_score_codex":0.0016755571,"about_ca_topic_score_gemma":0.0052618333,"teacher_disagreement_score":0.0016755571,"about_ca_system_score_codex":0.0004215339,"about_ca_system_score_gemma":0.0005040368,"threshold_uncertainty_score":0.0053346753},"labels":[],"label_agreement":null},{"id":"W2258939248","doi":"10.1038/gim.2015.124","title":"The role of combined SNV and CNV burden in patients with distal symmetric polyneuropathy","year":2015,"lang":"en","type":"article","venue":"Genetics in Medicine","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":24,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Centre for Movement Disorders","funders":"National Institute of General Medical Sciences; National Institute of Neurological Disorders and Stroke; National Human Genome Research Institute; Eunice Kennedy Shriver National Institute of Child Health and Human Development; National Heart, Lung, and Blood Institute","keywords":"Copy-number variation; Exome sequencing; Gene duplication; Genetics; Locus (genetics); Comparative genomic hybridization; Biology; Exome; Genetic heterogeneity; Phenotype; Gene; Genome","score_opus":0.018071613701866357,"score_gpt":0.23438740318433923,"score_spread":0.21631578948247288,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2258939248","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":[0.9949882,0.0015881708,0.00024947218,0.000266103,0.000021979642,0.000005065824,0.00025638414,0.000013143333,0.0026115032],"genre_scores_gemma":[0.99926347,0.00020529807,0.00015400624,0.000033072847,0.000028274142,0.0000023537561,0.00010461488,0.000006296852,0.00020262938],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99928075,0.0001790444,0.00006965081,0.00021174004,0.00015253798,0.00010624855],"domain_scores_gemma":[0.9973183,0.0013559782,0.0007049954,0.00010776054,0.00022682159,0.00028602444],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0005349623,0.0006917722,0.0005351884,0.0017657063,0.0006190821,0.0012235759,0.0007111382,0.001129931,0.0049487865],"category_scores_gemma":[0.0048904456,0.0003094719,0.00040999445,0.0013275949,0.00060171605,0.0011859027,0.0006637255,0.00055667775,0.00043215172],"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":[0.0006639352,0.00004366425,0.9764687,0.00004377044,0.00017004255,0.005244622,0.00015077942,0.00033145433,0.0054219314,0.00034783586,0.00032462613,0.010788698],"study_design_scores_gemma":[0.000021517806,0.00018795524,0.97378236,0.000051550003,0.00023773209,0.020783437,0.00040770642,0.00163818,0.0010696093,0.0011603985,0.0006322418,0.000027446886],"about_ca_topic_score_codex":0.0027433503,"about_ca_topic_score_gemma":0.0030161936,"teacher_disagreement_score":0.0049487865,"about_ca_system_score_codex":0.00041648635,"about_ca_system_score_gemma":0.000478755,"threshold_uncertainty_score":0.016555369},"labels":[],"label_agreement":null},{"id":"W2281372158","doi":"10.1089/acm.2006.12.703","title":"Neural Therapy: Applied Physiology and Other Topics Robert F. Kidd , M.D., C.M. <i>Renfrew, Ontario, Canada: Custom Distribution</i> , 2005, 203 pages, ISBN 0-9737800-0-2, $79.95, hardcover","year":2006,"lang":"en","type":"article","venue":"The Journal of Alternative and Complementary Medicine","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":0,"is_retracted":false,"has_abstract":false,"route_ca_aff":false,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":true,"ca_institutions":"","funders":"","keywords":"Medicine; Download; Library science; Physiology; Cognitive science; Computer science; World Wide Web; Psychology","score_opus":0.03326549609623944,"score_gpt":0.25041936397134884,"score_spread":0.2171538678751094,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2281372158","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":[0.0009664112,0.8446068,0.0057658064,0.01644256,0.017938284,0.000052207582,0.000108716595,0.00022259829,0.11389655],"genre_scores_gemma":[0.0077492767,0.7299248,0.0028262255,0.0026729177,0.012349472,0.000059518035,0.00011734711,0.00012866555,0.2441718],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.99970263,0.00004785841,0.000022685108,0.00003832651,0.00015805458,0.000030504587],"domain_scores_gemma":[0.9994537,0.00022266852,0.000026062358,0.000027000395,0.00013940474,0.00013106895],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0011247848,0.0011727386,0.0011739632,0.0021396626,0.00048548286,0.0027462363,0.00072920026,0.0013602524,0.07967256],"category_scores_gemma":[0.00087867136,0.00022652549,0.00059634954,0.0014007643,0.0011045471,0.0021603124,0.0010186009,0.0016823787,0.026698377],"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":[0.00010478418,0.000080011494,0.00015259201,0.0016313972,0.000020639072,0.00020010839,0.00017936334,0.00032920827,0.0034359114,0.005701053,0.3804648,0.60770017],"study_design_scores_gemma":[0.000014432531,0.00010218374,0.00084141997,0.0009159316,0.000010767992,0.001177457,0.00012223625,0.00022393005,0.0005310295,0.006167013,0.98988056,0.0000130446515],"about_ca_topic_score_codex":0.0018564183,"about_ca_topic_score_gemma":0.0050075348,"teacher_disagreement_score":0.07967256,"about_ca_system_score_codex":0.00091932766,"about_ca_system_score_gemma":0.0008139997,"threshold_uncertainty_score":0.2665313},"labels":[],"label_agreement":null},{"id":"W2304483068","doi":"10.1093/jnen/62.7.751","title":"Phenotypic Differences between Peripheral Myelin Protein-22 (PMP22) and Myelin Protein Zero (P<sub>0</sub>) Mutations Associated with Charcot-Marie-Tooth-Related Diseases","year":2003,"lang":"en","type":"article","venue":"Journal of Neuropathology & Experimental Neurology","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":55,"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":"McGill University","keywords":"Biology; Endoplasmic reticulum; Peripheral myelin protein 22; Myelin; Calnexin; Phenotype; Mutant; Green fluorescent protein; Cell biology; Transfection; Intracellular; Molecular biology; Gene; Genetics; Calreticulin; Central nervous system","score_opus":0.01914404292910578,"score_gpt":0.24110966241188275,"score_spread":0.221965619482777,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2304483068","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":[0.9990125,0.00022004895,0.0002955885,0.000015510388,0.0000043172495,0.000004619879,0.00008195908,0.000013409497,0.0003521339],"genre_scores_gemma":[0.9985697,0.00023434461,0.0004087058,0.000035932702,0.000004491624,0.000013897964,0.00017824258,0.000016402844,0.000538227],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9998266,0.000033383294,0.00002540527,0.00004831701,0.000041980707,0.000024327732],"domain_scores_gemma":[0.99979275,0.00003740433,0.00005477429,0.000013034923,0.000021499603,0.00008057436],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00013951788,0.0004754152,0.00021298804,0.00036302657,0.00014894169,0.00024428335,0.00015707489,0.00031952147,0.001077861],"category_scores_gemma":[0.0004287339,0.00017536743,0.00019190041,0.00013613651,0.00028106396,0.00018567417,0.00039460027,0.0002597029,0.00030658636],"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":[0.0002497048,0.000033887525,0.0040407875,0.00002340373,0.000015321617,0.001426761,0.000066657296,0.00005773799,0.9930281,0.00006873546,0.000046919395,0.0009420881],"study_design_scores_gemma":[0.00011064871,0.0013628617,0.4056797,0.00002501301,0.00013721555,0.06793353,0.00047198744,0.0018762382,0.5187327,0.0003992698,0.003215429,0.000055422075],"about_ca_topic_score_codex":0.0003079039,"about_ca_topic_score_gemma":0.00030091227,"teacher_disagreement_score":0.001077861,"about_ca_system_score_codex":0.00014667863,"about_ca_system_score_gemma":0.00008833206,"threshold_uncertainty_score":0.003605783},"labels":[],"label_agreement":null},{"id":"W2313602731","doi":"10.1017/s0317167100006065","title":"SPG4 Founder Effect in French Canadians with Hereditary Spastic Paraplegia","year":2007,"lang":"en","type":"article","venue":"Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":7,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":true,"route_about_ca":true,"ca_institutions":"Université de Sherbrooke; Centre Hospitalier Universitaire de Sherbrooke; Hôpital Notre-Dame","funders":"Fonds de Recherche du Québec - Santé; Canadian Institutes of Health Research","keywords":"Hereditary spastic paraplegia; Founder effect; Medicine; Spastic; Paraplegia; Physical medicine and rehabilitation; Pediatrics; Genealogy; Genetics; History; Biology; Psychiatry; Cerebral palsy; Spinal cord; Genotype; Phenotype; Gene","score_opus":0.028964837921488545,"score_gpt":0.2630479408412309,"score_spread":0.23408310291974235,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2313602731","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":[0.9907844,0.001024831,0.00036176393,0.0004667455,0.00003699798,0.000055829336,0.0013589889,0.000032974855,0.005877426],"genre_scores_gemma":[0.996539,0.00045147265,0.0004862111,0.00017546937,0.000014577051,0.000014593715,0.00045156435,0.000014097713,0.0018529716],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9993051,0.000066463384,0.000034919558,0.0001620427,0.0002352102,0.00019626458],"domain_scores_gemma":[0.99913603,0.0001123365,0.00014259997,0.000037658458,0.00039858397,0.00017294103],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00050375675,0.00090440706,0.00042424595,0.0025279003,0.004950858,0.0006230934,0.0008366322,0.0006470463,0.0079093715],"category_scores_gemma":[0.0018819316,0.00024737293,0.0005335067,0.002524142,0.00082653365,0.00015513983,0.00063089223,0.0005654433,0.0003104471],"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":[0.00055041,0.000118670556,0.93111324,0.00014152194,0.00022059452,0.016348325,0.00439971,0.00034262802,0.005420744,0.0012358718,0.005362521,0.03474577],"study_design_scores_gemma":[0.000055144552,0.000166702,0.9649455,0.00012951638,0.000235264,0.0179941,0.002849161,0.0006373935,0.0009010218,0.0002508156,0.011772611,0.00006267676],"about_ca_topic_score_codex":0.95923346,"about_ca_topic_score_gemma":0.9640137,"teacher_disagreement_score":0.040766537,"about_ca_system_score_codex":0.009335208,"about_ca_system_score_gemma":0.009397978,"threshold_uncertainty_score":0.08201319},"labels":[],"label_agreement":null},{"id":"W2315803217","doi":"10.1017/s0317167100010398","title":"Charcot Ankle Arthropathy in CMT1A Exacerbated by Type 2 Diabetes Mellitus","year":2010,"lang":"en","type":"article","venue":"Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":6,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":true,"route_about_ca":false,"ca_institutions":"Dalhousie University","funders":"","keywords":"Ankle; Arthropathy; Medicine; Diabetes mellitus; Type 2 Diabetes Mellitus; Physical medicine and rehabilitation; Surgery; Endocrinology; Osteoarthritis; Pathology; Alternative medicine","score_opus":0.028515259345592774,"score_gpt":0.2550021455117835,"score_spread":0.22648688616619075,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2315803217","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":[0.98286265,0.0025737814,0.00035326014,0.0015436923,0.00021299449,0.00008774794,0.000288328,0.00005181673,0.0120257],"genre_scores_gemma":[0.996777,0.0011175647,0.00023641736,0.00042458446,0.00035260417,0.000017012037,0.0001351108,0.000008034829,0.0009317374],"study_design_codex":"case_report","study_design_gemma":"case_report","domain_scores_codex":[0.9996269,0.00006790583,0.000053662225,0.00005059353,0.00008947411,0.00011151684],"domain_scores_gemma":[0.99918014,0.00028405225,0.00024046605,0.00003553951,0.00006999536,0.00018978362],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00040315106,0.00070690864,0.0006873593,0.0015218722,0.000853538,0.00074274844,0.00042015724,0.0013685882,0.006530894],"category_scores_gemma":[0.0028450533,0.00038800007,0.0004949232,0.0016408531,0.00042480748,0.00065355265,0.0004731166,0.0011645489,0.00064296764],"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":[0.0017686035,0.0003880883,0.27429932,0.00023344651,0.00013095188,0.70003456,0.00029783044,0.00019715262,0.002743757,0.00026870467,0.0029824215,0.016655162],"study_design_scores_gemma":[0.00017707884,0.0004085575,0.43006656,0.00014943992,0.00015865949,0.5655928,0.00045359466,0.0006438358,0.0004425918,0.0004843761,0.0013876185,0.000034746066],"about_ca_topic_score_codex":0.007291942,"about_ca_topic_score_gemma":0.007452848,"teacher_disagreement_score":0.007291942,"about_ca_system_score_codex":0.0006614027,"about_ca_system_score_gemma":0.000556893,"threshold_uncertainty_score":0.021847963},"labels":[],"label_agreement":null},{"id":"W2316898509","doi":"10.1017/s0317167100005199","title":"A Novel GDAP1 Mutation 439delA is Associated with Autosomal Recessive CMT Disease","year":2006,"lang":"en","type":"article","venue":"Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":11,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":true,"route_about_ca":false,"ca_institutions":"SickKids Foundation; Hospital for Sick Children; University of Toronto","funders":"Muscular Dystrophy Association","keywords":"Genetics; Locus (genetics); Exon; Genetic linkage; Mutation; Gene; Family history; Consanguinity; Biology; Genetic heterogeneity; Medicine; Phenotype; Internal medicine","score_opus":0.033737592555452695,"score_gpt":0.2558096273592392,"score_spread":0.22207203480378648,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2316898509","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":[0.9984486,0.00020955528,0.00031145845,0.00012188388,0.000018392153,0.000017729577,0.00008953517,0.000030341931,0.00075230724],"genre_scores_gemma":[0.99878365,0.00009714528,0.00061502523,0.00006728473,0.000019778978,0.000007568017,0.00006818124,0.0000074117847,0.00033397693],"study_design_codex":"case_report","study_design_gemma":"observational","domain_scores_codex":[0.9997944,0.000018968518,0.000020446505,0.00008184009,0.00004669863,0.000037535145],"domain_scores_gemma":[0.9996338,0.00010289839,0.00011593255,0.000016104614,0.000026446762,0.000104828156],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00016742718,0.00114116,0.00044066485,0.0009754304,0.0007318858,0.00025097947,0.00051077787,0.0012382003,0.0021438794],"category_scores_gemma":[0.0008207185,0.00032750214,0.00035096283,0.0006867167,0.0006984923,0.00023118529,0.000577517,0.0006353178,0.0003126033],"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":[0.00027137354,0.00011891917,0.06653635,0.00011257613,0.00006209738,0.87284046,0.0008125705,0.00019009157,0.05354849,0.00039445364,0.00046297832,0.004649633],"study_design_scores_gemma":[0.000083097904,0.00028390318,0.09906628,0.00003884371,0.00007214151,0.89298946,0.00021834791,0.00053918327,0.0050780876,0.00024461106,0.0013577994,0.000028186085],"about_ca_topic_score_codex":0.0021894658,"about_ca_topic_score_gemma":0.0022348675,"teacher_disagreement_score":0.0021894658,"about_ca_system_score_codex":0.0004059223,"about_ca_system_score_gemma":0.0003984145,"threshold_uncertainty_score":0.007172048},"labels":[],"label_agreement":null},{"id":"W2317646220","doi":"10.1016/j.bbadis.2016.04.003","title":"Exclusive expression of the Rab11 effector SH3TC2 in Schwann cells links integrin-α6 and myelin maintenance to Charcot-Marie-Tooth disease type 4C","year":2016,"lang":"en","type":"article","venue":"Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":26,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Alberta","funders":"Cambridge Institute for Medical Research, University of Cambridge; Wellcome Trust","keywords":"Effector; Schwann cell; Myelin; Integrin; Cell biology; Biology; Neuroscience; Genetics; Cell","score_opus":0.011271984233726,"score_gpt":0.23890620996209205,"score_spread":0.22763422572836606,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2317646220","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":[0.99808997,0.0005106249,0.0005395923,0.000043921165,0.000008152323,0.000002224298,0.000087639535,0.000021660224,0.0006960391],"genre_scores_gemma":[0.998528,0.000212897,0.00022388103,0.000017994484,0.000003981986,0.000003917556,0.00015660372,0.0000037893458,0.00084908376],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9999491,0.0000050106705,0.0000038429575,0.000012634193,0.000014472014,0.0000150552605],"domain_scores_gemma":[0.9999335,0.000007719,0.000024931644,0.0000054877764,0.000009099083,0.000019318797],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.000059482172,0.00020901438,0.000119755256,0.00020236665,0.00018491146,0.00020757233,0.00012133183,0.00027691538,0.0008348882],"category_scores_gemma":[0.000107759915,0.000074694646,0.0001301055,0.00013599289,0.00022757998,0.00009742483,0.0002470114,0.00027269043,0.00028502755],"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":[0.00011470746,0.000007249229,0.0017705811,0.000016412894,0.0000044747153,0.00074932666,0.000018262333,0.000050394447,0.9964533,0.000110536545,0.00004287367,0.0006619056],"study_design_scores_gemma":[0.000036672784,0.00019613554,0.14943051,0.000017737604,0.000058328722,0.009065286,0.00015792236,0.0022731682,0.83209336,0.0003695775,0.006289424,0.00001184097],"about_ca_topic_score_codex":0.0010536606,"about_ca_topic_score_gemma":0.001188104,"teacher_disagreement_score":0.0010536606,"about_ca_system_score_codex":0.0002537673,"about_ca_system_score_gemma":0.00016149867,"threshold_uncertainty_score":0.0027929544},"labels":[],"label_agreement":null},{"id":"W2318852518","doi":"10.1017/s0317167100006831","title":"Tumefactive Demyelinating Lesions","year":2007,"lang":"fr","type":"article","venue":"Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":5,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":true,"route_about_ca":false,"ca_institutions":"Health Sciences Centre; University of Calgary","funders":"","keywords":"Demyelinating disease; Medicine; Content (measure theory); Action (physics); Pathology; Physics; Mathematics; Disease","score_opus":0.06076435923863059,"score_gpt":0.30372904950751134,"score_spread":0.24296469026888073,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2318852518","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":[0.9609247,0.0041468535,0.0011314799,0.0015319147,0.00015460327,0.00015671866,0.0006913053,0.00018248851,0.031080015],"genre_scores_gemma":[0.9945378,0.001109853,0.00044670145,0.000326184,0.00008577146,0.000013201234,0.00015182729,0.000009551644,0.003319298],"study_design_codex":"case_report","study_design_gemma":"case_report","domain_scores_codex":[0.9998305,0.000014016897,0.000014668806,0.000047055008,0.000027608818,0.00006614263],"domain_scores_gemma":[0.9997185,0.00007286636,0.000041262694,0.000024389397,0.000032086326,0.00011092266],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00021189608,0.0012623011,0.00054662704,0.0011937943,0.0011910843,0.00066438806,0.00046674057,0.0012611258,0.0040906235],"category_scores_gemma":[0.00083204336,0.00029889538,0.00022100953,0.0008896387,0.00058250845,0.00061927654,0.00045856918,0.00087011827,0.00073716126],"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":[0.00016133137,0.00005318718,0.009602982,0.00008240031,0.000015941461,0.9783508,0.00026818275,0.00008465999,0.005345175,0.00046323423,0.0003418567,0.0052301385],"study_design_scores_gemma":[0.000034433135,0.00025056722,0.02334508,0.000030357533,0.000020943453,0.9721327,0.00018565908,0.00024044844,0.0012094405,0.0003665974,0.0021691076,0.000014592957],"about_ca_topic_score_codex":0.0029205894,"about_ca_topic_score_gemma":0.0038424195,"teacher_disagreement_score":0.0040906235,"about_ca_system_score_codex":0.0007082333,"about_ca_system_score_gemma":0.00039913264,"threshold_uncertainty_score":0.013684571},"labels":[],"label_agreement":null},{"id":"W2324216196","doi":"10.1016/j.nmd.2016.04.006","title":"Response","year":2016,"lang":"en","type":"letter","venue":"Neuromuscular Disorders","topic":"Hereditary Neurological Disorders","field":"Neuroscience","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":"University of Toronto; Hospital for Sick Children","funders":"","keywords":"Medicine; Carpal tunnel syndrome; Entrapment Neuropathy; Carpal tunnel; Ulnar nerve; Weakness; Pediatrics; Surgery; Anatomy; Elbow","score_opus":0.024328727602344082,"score_gpt":0.2429549544082319,"score_spread":0.2186262268058878,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2324216196","genre_codex":"commentary","genre_gemma":"commentary","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"commentary","genre_consensus":"commentary","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.0005979434,0.0009847914,0.00012313316,0.9462266,0.041870557,0.000056167057,0.00015925424,0.00009866655,0.009882905],"genre_scores_gemma":[0.0037551916,0.0007048236,0.00012538701,0.93548006,0.029486546,0.00007889861,0.00008015545,0.000030000732,0.03025887],"study_design_codex":"not_applicable","study_design_gemma":"not_applicable","domain_scores_codex":[0.997983,0.000378444,0.00021538878,0.00036228888,0.00050119223,0.000559658],"domain_scores_gemma":[0.99579275,0.0016949134,0.0004356947,0.00014796428,0.00090857287,0.0010201127],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0015790857,0.0010189761,0.0016289162,0.0009824109,0.00474615,0.004867835,0.0023188828,0.06847371,0.031787593],"category_scores_gemma":[0.020815343,0.00085024524,0.0015576459,0.0005651477,0.0022888235,0.002313379,0.0023511348,0.036984295,0.02122784],"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":[0.000050353043,0.0000198242,0.0005978451,0.000051919124,0.000015002987,0.0030562547,0.000097462434,0.00007143259,0.00010137245,0.001034722,0.9902975,0.00460634],"study_design_scores_gemma":[0.00016188178,0.00010036927,0.0018783173,0.00065612665,0.000049650345,0.004780361,0.00084968755,0.00063828746,0.0002718165,0.0073008086,0.98321587,0.00009695031],"about_ca_topic_score_codex":0.00586406,"about_ca_topic_score_gemma":0.009862234,"teacher_disagreement_score":0.06847371,"about_ca_system_score_codex":0.004749573,"about_ca_system_score_gemma":0.004129983,"threshold_uncertainty_score":0},"labels":[],"label_agreement":null},{"id":"W2326030097","doi":"10.1097/bpb.0b013e328347fada","title":"Limited atlantooccipital and cervical range of motion in patients with familial dysautonomia","year":2011,"lang":"en","type":"article","venue":"Journal of Pediatric Orthopaedics B","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":3,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Ottawa","funders":"","keywords":"Medicine; Familial dysautonomia; Sagittal plane; Cervical spine; Kyphoscoliosis; Range of motion; Cervical vertebrae; Radiography; Orthodontics; Surgery; Anatomy; Scoliosis; Internal medicine","score_opus":0.02175651072816749,"score_gpt":0.2026433915436113,"score_spread":0.1808868808154438,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2326030097","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":[0.9993098,0.0002342657,0.00003308656,0.000028719247,0.0000030155534,0.0000030056995,0.000040331077,0.000003958226,0.0003439452],"genre_scores_gemma":[0.9997985,0.000064016815,0.000030415973,0.000013560614,0.0000054093907,0.0000023028947,0.00003836237,8.158419e-7,0.000046735357],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99975234,0.00003926273,0.000041509433,0.00007310298,0.000050941715,0.00004289346],"domain_scores_gemma":[0.9993186,0.00018422378,0.00028467522,0.000028737746,0.000055688593,0.00012805453],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0002062175,0.0005345005,0.00043161074,0.0012290968,0.000744413,0.00041922665,0.00025831308,0.0005563855,0.001373229],"category_scores_gemma":[0.0022678776,0.00027681718,0.00018578184,0.00074578094,0.00062397856,0.00030657378,0.00031713487,0.00029897972,0.00013868135],"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":[0.00026944972,0.000054031458,0.9770408,0.000026544245,0.000047131794,0.015957823,0.00050605246,0.000089543275,0.0023546624,0.000039563525,0.00017386847,0.003440441],"study_design_scores_gemma":[0.000018005006,0.00021724368,0.9629216,0.000012891845,0.00004229033,0.036010068,0.0003080984,0.0001022217,0.00016613389,0.000048497197,0.00014499303,0.000007906567],"about_ca_topic_score_codex":0.00435956,"about_ca_topic_score_gemma":0.005289549,"teacher_disagreement_score":0.00435956,"about_ca_system_score_codex":0.00035762653,"about_ca_system_score_gemma":0.00025614657,"threshold_uncertainty_score":0.008668423},"labels":[],"label_agreement":null},{"id":"W2327643467","doi":"10.5692/clinicalneurol.51.1125","title":"Hereditary spastic paraplegia in Japan","year":2011,"lang":"en","type":"article","venue":"Rinsho Shinkeigaku","topic":"Hereditary Neurological Disorders","field":"Neuroscience","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":"Hereditary spastic paraplegia; Paraplegia; Spastic; Medicine; Physical medicine and rehabilitation; Physical therapy; Biology; Genetics; Spinal cord; Gene; Cerebral palsy; Phenotype; Psychiatry","score_opus":0.09634395108413307,"score_gpt":0.2547818145460281,"score_spread":0.15843786346189503,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2327643467","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":[0.993718,0.002092382,0.00026862332,0.00012250549,0.000020820162,0.000027543592,0.00020011168,0.000024220131,0.003525765],"genre_scores_gemma":[0.9969175,0.0015301532,0.00025526507,0.00008779124,0.00002427053,0.00001493632,0.00029003495,0.0000042772017,0.0008758335],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99976903,0.000031897896,0.000034741868,0.00006259437,0.00004244906,0.000059207345],"domain_scores_gemma":[0.99982196,0.000013980518,0.00004620689,0.000009230676,0.000042662232,0.000065976936],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00016912654,0.00057346164,0.00034885577,0.0013390955,0.00089056866,0.0003478797,0.00015654185,0.00025530174,0.0019722118],"category_scores_gemma":[0.00033683155,0.00020276876,0.00031919996,0.0014956995,0.00036018892,0.0001895122,0.0005741384,0.00016860839,0.00019918845],"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":[0.00055004883,0.00021317875,0.8315814,0.00044541166,0.0004474634,0.06341855,0.0027794354,0.00047314656,0.029249081,0.0013325141,0.0048767915,0.06463288],"study_design_scores_gemma":[0.00008002439,0.0002679501,0.9522638,0.00010262662,0.00023617034,0.039444514,0.0009117835,0.0004755956,0.0008972059,0.0002933953,0.0050033582,0.000023646366],"about_ca_topic_score_codex":0.045748733,"about_ca_topic_score_gemma":0.051423013,"teacher_disagreement_score":0.045748733,"about_ca_system_score_codex":0.00075599976,"about_ca_system_score_gemma":0.000814102,"threshold_uncertainty_score":0.09096491},"labels":[],"label_agreement":null},{"id":"W2328710648","doi":"10.1017/s0317167100006879","title":"Management of Isolated Demyelinating Episodes by North American Neurologists","year":2007,"lang":"en","type":"letter","venue":"Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":0,"is_retracted":false,"has_abstract":true,"route_ca_aff":false,"route_ca_fund":false,"route_ca_venue":true,"route_about_ca":false,"ca_institutions":"","funders":"","keywords":"Demyelinating disease; Action (physics); Medicine; Content (measure theory); Psychology; Multiple sclerosis; Psychiatry; Physics","score_opus":0.03735774918786174,"score_gpt":0.27600579977844886,"score_spread":0.2386480505905871,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2328710648","genre_codex":"empirical","genre_gemma":"commentary","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"commentary","genre_consensus":null,"domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.5702704,0.05280773,0.0034705745,0.14278366,0.0057331775,0.00018479119,0.0003283664,0.00042034604,0.2240009],"genre_scores_gemma":[0.9510532,0.016208412,0.0010487451,0.0155611485,0.0069937343,0.000055015855,0.00017335075,0.000034403358,0.008872],"study_design_codex":"case_report","study_design_gemma":"observational","domain_scores_codex":[0.9996687,0.00008367659,0.000045557303,0.000048267702,0.000061753526,0.00009206796],"domain_scores_gemma":[0.99948907,0.00016854965,0.000098501565,0.000015767797,0.000060969185,0.00016709197],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00023018803,0.00033917325,0.00047529262,0.0008375467,0.0016611629,0.0006641643,0.0003452973,0.001815237,0.0032801381],"category_scores_gemma":[0.0024845907,0.00014802042,0.000260923,0.00067014067,0.00042012244,0.0006261691,0.00035272466,0.001447371,0.0008226717],"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":[0.0006122608,0.00055720727,0.102650166,0.00063484674,0.00013338507,0.55711144,0.0010402077,0.0007853301,0.0023730039,0.0015233657,0.16424161,0.1683372],"study_design_scores_gemma":[0.0002658637,0.00037035707,0.09237709,0.00095121283,0.00010676288,0.8498902,0.0012239204,0.0018655991,0.0009734104,0.0032403565,0.04868367,0.000051535753],"about_ca_topic_score_codex":0.0037501971,"about_ca_topic_score_gemma":0.009060289,"teacher_disagreement_score":0.0037501971,"about_ca_system_score_codex":0.000788566,"about_ca_system_score_gemma":0.00086161424,"threshold_uncertainty_score":0.0109731555},"labels":[],"label_agreement":null},{"id":"W2329726124","doi":"10.1097/mao.0b013e31828f47a8","title":"Charcot-Marie-Tooth Disease as a Cause of Conductive Hearing Loss","year":2013,"lang":"en","type":"article","venue":"Otology & Neurotology","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":4,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":true,"ca_institutions":"Hôpital Notre-Dame","funders":"","keywords":"Medicine; Otorhinolaryngology; University hospital; Reprint; Head and neck surgery; Conductive hearing loss; Family medicine; Hearing loss; General surgery; Gerontology; Library science; Audiology; Surgery","score_opus":0.05243651869555955,"score_gpt":0.29365393339945284,"score_spread":0.2412174147038933,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2329726124","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":[0.92813003,0.010678193,0.001054684,0.0068703666,0.0010368844,0.00026037544,0.00055044255,0.00018092581,0.05123807],"genre_scores_gemma":[0.9935087,0.001663172,0.00032635592,0.00081521046,0.0005747302,0.000015475345,0.00010966189,0.000015703105,0.0029710792],"study_design_codex":"case_report","study_design_gemma":"observational","domain_scores_codex":[0.99938583,0.00006362595,0.00004363324,0.00008310822,0.00018212415,0.000241673],"domain_scores_gemma":[0.99901617,0.00024669073,0.00011243341,0.000039818,0.00013694994,0.00044790085],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00040937014,0.0015864854,0.0007122407,0.0022711968,0.0021943883,0.0010033771,0.0013717193,0.0025083392,0.0051544784],"category_scores_gemma":[0.0017786515,0.0005507355,0.00040943065,0.0014861624,0.002114901,0.00061740953,0.0009320958,0.0018248769,0.0008778128],"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":[0.00007953673,0.00005723186,0.016891662,0.000042985448,0.000026856618,0.9768262,0.00016614248,0.000092972085,0.0010369451,0.00046664377,0.0017734838,0.0025394065],"study_design_scores_gemma":[0.000081417136,0.00009301649,0.06824958,0.000100774516,0.000079998244,0.92660064,0.00034610418,0.00053598604,0.00064321334,0.00071160466,0.0025117868,0.00004593247],"about_ca_topic_score_codex":0.086463995,"about_ca_topic_score_gemma":0.12278824,"teacher_disagreement_score":0.086463995,"about_ca_system_score_codex":0.0031755902,"about_ca_system_score_gemma":0.00405198,"threshold_uncertainty_score":0.17192143},"labels":[],"label_agreement":null},{"id":"W2330590789","doi":"10.1017/cjn.2016.17","title":"Novel <i>SPG 11</i> Mutations in Hereditary Spastic Paraplegia With Thin Corpus Callosum in a Chinese Family","year":2016,"lang":"en","type":"article","venue":"Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":4,"is_retracted":false,"has_abstract":true,"route_ca_aff":false,"route_ca_fund":false,"route_ca_venue":true,"route_about_ca":false,"ca_institutions":"","funders":"","keywords":"Hereditary spastic paraplegia; Corpus callosum; Paraplegia; Chinese family; Medicine; Spastic; Mutation; Genetics; Anatomy; Biology; Physical medicine and rehabilitation; Phenotype; Gene; Spinal cord; Psychiatry; Cerebral palsy","score_opus":0.03490632932420097,"score_gpt":0.2577206446942959,"score_spread":0.22281431537009494,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2330590789","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":[0.998629,0.000088109016,0.0003161914,0.0000814371,0.000010895685,0.00003137689,0.00007768033,0.000015429725,0.00074987573],"genre_scores_gemma":[0.9990834,0.00006076748,0.00034157874,0.00006125671,0.000012640868,0.0000137893785,0.00007483986,0.000005538705,0.00034626928],"study_design_codex":"case_report","study_design_gemma":"observational","domain_scores_codex":[0.9998011,0.000020039619,0.000028445558,0.00006972178,0.000038899198,0.000041786152],"domain_scores_gemma":[0.99971324,0.00007135223,0.00007411722,0.000017091334,0.000031904146,0.00009220764],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00026303786,0.0013715912,0.0004969647,0.0011334232,0.0017598186,0.00026743565,0.00058287615,0.00072600826,0.0023379193],"category_scores_gemma":[0.0005494111,0.00031647793,0.0005543517,0.00095735193,0.0009976184,0.00019844211,0.00057617907,0.00041752428,0.00025578417],"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":[0.00042628424,0.0002670653,0.16666946,0.00020700892,0.00020801704,0.7456041,0.0040388466,0.00075136044,0.06866196,0.00087366224,0.0008478564,0.011444479],"study_design_scores_gemma":[0.0001394607,0.0008086456,0.5047288,0.00008073252,0.0004820927,0.467895,0.001158985,0.0020634667,0.018499264,0.0007530817,0.0032920686,0.00009838025],"about_ca_topic_score_codex":0.009234771,"about_ca_topic_score_gemma":0.009347723,"teacher_disagreement_score":0.009234771,"about_ca_system_score_codex":0.00061669113,"about_ca_system_score_gemma":0.00085485575,"threshold_uncertainty_score":0.018362045},"labels":[],"label_agreement":null},{"id":"W2332164501","doi":"10.1155/2001/518043","title":"Anticipation in an Indo-Canadian Family with Crohn's Disease","year":2001,"lang":"en","type":"article","venue":"Canadian Journal of Gastroenterology","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":10,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":true,"route_about_ca":true,"ca_institutions":"University of Calgary; University of British Columbia","funders":"","keywords":"Anticipation (artificial intelligence); Disease; Crohn's disease; Medicine; Population; Inflammatory bowel disease; Genetic predisposition; Pathology","score_opus":0.033678503337118255,"score_gpt":0.2477759436712641,"score_spread":0.21409744033414585,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2332164501","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":[0.99061865,0.00058787066,0.00028348758,0.0007385803,0.000036817186,0.000030308945,0.0002295284,0.000022468046,0.0074523785],"genre_scores_gemma":[0.99567634,0.0007534036,0.0006245027,0.0002896733,0.00002713606,0.000009447631,0.000112261085,0.0000095684545,0.0024977308],"study_design_codex":"case_report","study_design_gemma":"case_report","domain_scores_codex":[0.9997135,0.000020300839,0.000011196893,0.000060971186,0.00008675163,0.00010729685],"domain_scores_gemma":[0.9996257,0.0000477886,0.0000566567,0.0000151476015,0.00007709986,0.00017764088],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00015511722,0.000880441,0.00036982365,0.0010172359,0.006300831,0.0005909326,0.00044534873,0.0007522388,0.0028848231],"category_scores_gemma":[0.0011210402,0.000304921,0.00032543088,0.0014554572,0.0009144617,0.0002078603,0.00081025256,0.00086583995,0.0002114841],"study_design_candidate":"case_report","study_design_consensus":"case_report","about_ca_topic_candidate":true,"about_ca_topic_consensus":true,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0006996898,0.00022741166,0.37504673,0.00012209691,0.000088764304,0.5545139,0.013115995,0.000655396,0.015417751,0.0024773637,0.0038659873,0.033769026],"study_design_scores_gemma":[0.00007111448,0.00035126603,0.42592236,0.00013567513,0.00021643897,0.55036575,0.0059700026,0.0010924778,0.003059267,0.0007921113,0.011840612,0.0001829058],"about_ca_topic_score_codex":0.6801118,"about_ca_topic_score_gemma":0.8293645,"teacher_disagreement_score":0.31988817,"about_ca_system_score_codex":0.0043962877,"about_ca_system_score_gemma":0.0063409703,"threshold_uncertainty_score":0.6435441},"labels":[],"label_agreement":null},{"id":"W2335273140","doi":"10.1017/s0317167100007290","title":"A Novel GDAP1 Mutation P78L Responsible for CMT4A Disease in Three Moroccan Families","year":2007,"lang":"en","type":"article","venue":"Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":14,"is_retracted":false,"has_abstract":true,"route_ca_aff":false,"route_ca_fund":false,"route_ca_venue":true,"route_about_ca":false,"ca_institutions":"","funders":"Centre National pour la Recherche Scientifique et Technique","keywords":"Haplotype; Genetics; Mutation; Exon; Biology; Gene; Phenotype; Transversion; Coding region; Genotype","score_opus":0.064055677205026,"score_gpt":0.29905468027490223,"score_spread":0.23499900306987623,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2335273140","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":[0.9988611,0.00019137084,0.0002081104,0.00010713577,0.000011793,0.000016462864,0.00007607445,0.0000130338585,0.0005148358],"genre_scores_gemma":[0.99891794,0.000095717194,0.00043946848,0.0000801728,0.000013568829,0.000013830632,0.00007784595,0.000009242422,0.00035218705],"study_design_codex":"case_report","study_design_gemma":"observational","domain_scores_codex":[0.99962986,0.00004613919,0.00003253398,0.0001181037,0.000073837095,0.000099507364],"domain_scores_gemma":[0.99956006,0.00012132902,0.00010885773,0.000022697497,0.000058945752,0.0001279951],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00022019699,0.0019109962,0.0006388157,0.0016015955,0.0024677822,0.0004786952,0.0007365384,0.0010746754,0.0024358043],"category_scores_gemma":[0.001422319,0.00044992255,0.00053519406,0.00076828635,0.0010734596,0.00022036502,0.0009458466,0.0006252236,0.0002395],"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":[0.0005572194,0.00020676307,0.19123617,0.00011979546,0.00012988491,0.7423948,0.006214385,0.0004147497,0.03966354,0.0006381589,0.0007769082,0.017647551],"study_design_scores_gemma":[0.000117225645,0.00039596498,0.25580934,0.00007872951,0.00017595103,0.7323604,0.0013737899,0.0007349663,0.005531539,0.00039214388,0.0029522565,0.000077709345],"about_ca_topic_score_codex":0.015399271,"about_ca_topic_score_gemma":0.010610616,"teacher_disagreement_score":0.015399271,"about_ca_system_score_codex":0.0014747349,"about_ca_system_score_gemma":0.00074313505,"threshold_uncertainty_score":0.030619264},"labels":[],"label_agreement":null},{"id":"W2335414527","doi":"10.1017/s0317167100016139","title":"Pure Dermatomal Sensory Deficits in Lateral Medullary Infarction","year":2013,"lang":"en","type":"letter","venue":"Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":2,"is_retracted":false,"has_abstract":true,"route_ca_aff":false,"route_ca_fund":false,"route_ca_venue":true,"route_about_ca":false,"ca_institutions":"","funders":"","keywords":"Medullary cavity; Sensory system; Medicine; Infarction; Neuroscience; Psychology; Anatomy; Cardiology; Myocardial infarction","score_opus":0.04281551180191223,"score_gpt":0.25565455365086115,"score_spread":0.21283904184894892,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2335414527","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":[0.785521,0.007292212,0.0026809948,0.059357837,0.002447483,0.00031116017,0.0007020168,0.000671261,0.14101604],"genre_scores_gemma":[0.98145664,0.0018381849,0.0005330224,0.0053171185,0.0034936152,0.000035684643,0.000102216814,0.000041764953,0.0071818824],"study_design_codex":"case_report","study_design_gemma":"case_report","domain_scores_codex":[0.9996075,0.000048952996,0.000037528982,0.000079212514,0.000096255324,0.00013056013],"domain_scores_gemma":[0.99894637,0.0005035456,0.00014215431,0.000082337996,0.00007969672,0.00024589885],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0004482622,0.0013776716,0.0010719814,0.0017551049,0.0017499169,0.0015661318,0.0011909725,0.005268786,0.0065403245],"category_scores_gemma":[0.0038934057,0.00063959055,0.00060772075,0.0015702298,0.0021399446,0.0017026105,0.00089684833,0.0035748393,0.0015457909],"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":[0.00010194334,0.00005055999,0.00330122,0.00005023158,0.0000151636705,0.99009985,0.00007327035,0.0001505957,0.0006701053,0.0006444687,0.0026502025,0.0021923052],"study_design_scores_gemma":[0.00014317098,0.00012044162,0.021224773,0.00009163432,0.00005182432,0.9711041,0.00020723145,0.0012317951,0.00082555204,0.0030558088,0.001913734,0.000029983636],"about_ca_topic_score_codex":0.00631998,"about_ca_topic_score_gemma":0.008873301,"teacher_disagreement_score":0.0065403245,"about_ca_system_score_codex":0.0027752605,"about_ca_system_score_gemma":0.0012806369,"threshold_uncertainty_score":0.021879554},"labels":[],"label_agreement":null},{"id":"W2337291532","doi":"10.1017/s0317167100054184","title":"Multiple Brain Cysts: An Unusual Form of Demyelinating Disease","year":2011,"lang":"en","type":"article","venue":"Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":4,"is_retracted":false,"has_abstract":true,"route_ca_aff":false,"route_ca_fund":false,"route_ca_venue":true,"route_about_ca":false,"ca_institutions":"","funders":"","keywords":"Demyelinating disease; Action (physics); Medicine; Content (measure theory); Neuroscience; Disease; Psychology; Pathology; Physics; Mathematics","score_opus":0.08213776617985867,"score_gpt":0.2858232771342963,"score_spread":0.2036855109544376,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2337291532","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":[0.9716163,0.003225408,0.0043485262,0.0029789777,0.0003229825,0.00020447033,0.0006719706,0.00032286794,0.016308546],"genre_scores_gemma":[0.99503136,0.0007547412,0.0018686082,0.00030186956,0.00046614316,0.00003019696,0.000098437704,0.00004395048,0.0014046978],"study_design_codex":"case_report","study_design_gemma":"case_report","domain_scores_codex":[0.99924564,0.00007714974,0.00010048128,0.00020449834,0.00015887967,0.00021332508],"domain_scores_gemma":[0.99708444,0.0012105145,0.0005934376,0.00031638835,0.00013298963,0.00066214363],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00031202237,0.0020928085,0.0016724819,0.0035162338,0.0018048933,0.0020192734,0.0013365408,0.004405639,0.0038257192],"category_scores_gemma":[0.0044403495,0.0013687029,0.0005746268,0.0026893714,0.0020345973,0.0024527048,0.0019452514,0.0034868359,0.0014272648],"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":[0.000038988008,0.000027816426,0.0028008486,0.000024869296,0.000008171957,0.99442106,0.000083235835,0.00006110659,0.00095957937,0.00021026727,0.00021801915,0.0011460426],"study_design_scores_gemma":[0.00001564075,0.000022977614,0.0023367968,0.000005567534,0.000005636972,0.99671257,0.000040484225,0.00012610757,0.00026867667,0.00027136324,0.00018774513,0.0000064783835],"about_ca_topic_score_codex":0.0014804644,"about_ca_topic_score_gemma":0.002075893,"teacher_disagreement_score":0.004405639,"about_ca_system_score_codex":0.000927681,"about_ca_system_score_gemma":0.0007551933,"threshold_uncertainty_score":0.012798309},"labels":[],"label_agreement":null},{"id":"W2344897797","doi":"10.1007/s12031-016-0760-5","title":"Tocotrienol Treatment in Familial Dysautonomia: Open-Label Pilot Study","year":2016,"lang":"en","type":"article","venue":"Journal of Molecular Neuroscience","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":10,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"McGill University","funders":"Dysautonomia Foundation","keywords":"Familial dysautonomia; Medicine; Tocotrienol; Internal medicine; Vitamin E; Endocrinology; Biology; Tocopherol; Antioxidant; Biochemistry","score_opus":0.11813016645023576,"score_gpt":0.3379777044888312,"score_spread":0.2198475380385954,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2344897797","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":[0.9955877,0.0010123991,0.0005020845,0.00012328818,0.00008049115,0.0014699461,0.0006144483,0.000038770195,0.00057090656],"genre_scores_gemma":[0.9921606,0.0018893225,0.0011014526,0.00028022545,0.0002213255,0.0020016273,0.0009134141,0.0000169044,0.0014151694],"study_design_codex":"randomized_trial","study_design_gemma":"nonrandomized_trial","domain_scores_codex":[0.999271,0.0002877163,0.000057802474,0.00014086306,0.00006957644,0.00017306932],"domain_scores_gemma":[0.9985291,0.0004932361,0.0001803313,0.00025250917,0.000087515364,0.0004572887],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.001184531,0.0017176487,0.003890973,0.0006266142,0.00091612124,0.0009678422,0.0010971214,0.0021767416,0.0071048397],"category_scores_gemma":[0.0011958178,0.00060036127,0.0019546035,0.0006474677,0.0022845468,0.0014469353,0.0005169834,0.0025232453,0.0010730482],"study_design_candidate":"nonrandomized_trial","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":[0.85775036,0.083631575,0.0013616163,0.0006324572,0.00071786053,0.00041327495,0.00020893493,0.0005078552,0.023219144,0.00014290064,0.0005207675,0.030893205],"study_design_scores_gemma":[0.39563265,0.59488887,0.0047957,0.000059305963,0.0005696886,0.00019775784,0.0001493089,0.00046387612,0.0022941371,0.00015936742,0.0007457176,0.00004359361],"about_ca_topic_score_codex":0.0019896557,"about_ca_topic_score_gemma":0.0030124048,"teacher_disagreement_score":0.0071048397,"about_ca_system_score_codex":0.0011140582,"about_ca_system_score_gemma":0.0014576794,"threshold_uncertainty_score":0.023768067},"labels":[],"label_agreement":null},{"id":"W2345540709","doi":"10.1016/j.ajhg.2016.04.002","title":"Mutations in CAPN1 Cause Autosomal-Recessive Hereditary Spastic Paraplegia","year":2016,"lang":"en","type":"article","venue":"The American Journal of Human Genetics","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":114,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Centre hospitalier universitaire de Québec; Université de Montréal; Hospital for Sick Children; University of Toronto; Western University; Women and Children’s Health Research Institute; University of Alberta; Université Laval; Centre Hospitalier de l’Université de Montréal; McGill University; SickKids Foundation; Montreal Neurological Institute and Hospital","funders":"National Heart, Lung, and Blood Institute; Canadian Institutes of Health Research; Canada Research Chairs; ALS Society of Canada","keywords":"Biology; Genetics; Frameshift mutation; Hereditary spastic paraplegia; Missense mutation; Exome sequencing; Mutation; Disease gene identification; Gene; Phenotype","score_opus":0.03764252907979099,"score_gpt":0.2978557607510884,"score_spread":0.2602132316712974,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2345540709","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":[0.98492557,0.0016214411,0.0019156191,0.0006928332,0.00032770788,0.00005254588,0.0009017873,0.00020469664,0.009357727],"genre_scores_gemma":[0.9970523,0.00027066498,0.00081792544,0.00018879917,0.00007879362,0.000012546757,0.00023662999,0.00003171907,0.001310669],"study_design_codex":"case_report","study_design_gemma":"observational","domain_scores_codex":[0.9997243,0.000037555496,0.000033648936,0.000058865095,0.00009743199,0.00004819463],"domain_scores_gemma":[0.9995493,0.000098348304,0.00015107098,0.000020880556,0.00004500614,0.0001352502],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00021837528,0.0016287497,0.0004169436,0.00089682743,0.00063805387,0.00034813248,0.0006201548,0.0014132673,0.0025679204],"category_scores_gemma":[0.00091830245,0.00020908055,0.00037178324,0.00065434765,0.00077633513,0.00018936409,0.00075858727,0.0004687906,0.00063343806],"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":[0.0018521202,0.0003501341,0.048882887,0.000461554,0.00035965405,0.5917884,0.00075529394,0.0040773875,0.3083308,0.003501498,0.010970784,0.028669517],"study_design_scores_gemma":[0.0004304039,0.0007286484,0.25606376,0.00031655797,0.00066035934,0.61617166,0.0007088571,0.01376227,0.08620197,0.0034260165,0.021347294,0.00018211869],"about_ca_topic_score_codex":0.0038890329,"about_ca_topic_score_gemma":0.0053839474,"teacher_disagreement_score":0.0038890329,"about_ca_system_score_codex":0.0006523967,"about_ca_system_score_gemma":0.0004939622,"threshold_uncertainty_score":0.008590519},"labels":[],"label_agreement":null},{"id":"W2346209181","doi":"10.3390/molecules21050588","title":"In Silico Investigation of Traditional Chinese Medicine for Potential Lead Compounds as SPG7 Inhibitors against Coronary Artery Disease","year":2016,"lang":"en","type":"article","venue":"Molecules","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":10,"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":"Division of Materials Research; China Medical University; Asia University; China Medical University Hospital","keywords":"Virtual screening; In silico; Pharmacology; Coronary artery disease; Medicine; Chemistry; Computational biology; Traditional medicine; Biology; Drug discovery; Biochemistry; Internal medicine; Gene","score_opus":0.032222627999236954,"score_gpt":0.2540846040486705,"score_spread":0.22186197604943356,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2346209181","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":[0.95217097,0.005214561,0.0160678,0.00089484773,0.00012396685,0.00039119425,0.005696986,0.00083603495,0.0186037],"genre_scores_gemma":[0.9712101,0.001921412,0.01843267,0.00029373768,0.000031287225,0.00027301765,0.004971383,0.00007928145,0.0027871525],"study_design_codex":"simulation_or_modeling","study_design_gemma":"simulation_or_modeling","domain_scores_codex":[0.9998287,0.000048261205,0.000010303703,0.000032544358,0.00003797354,0.000042192558],"domain_scores_gemma":[0.99958616,0.0002837655,0.000038640846,0.000011797961,0.000047687416,0.000031961485],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0005145763,0.0013286802,0.0020390402,0.0012283109,0.0006136713,0.0010320408,0.0009156168,0.00069339457,0.007853533],"category_scores_gemma":[0.00093102007,0.00043924063,0.0019427883,0.0008640148,0.00024080284,0.00047618416,0.00051658956,0.0004692354,0.0005437606],"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":[0.00092894165,0.00043160206,0.013381922,0.0011530883,0.0006256911,0.0011915307,0.000052101226,0.9575302,0.007865539,0.003233904,0.0023561628,0.0112492675],"study_design_scores_gemma":[0.00027466865,0.0007697732,0.0017112786,0.00004913486,0.0004840971,0.0001510033,0.000073128234,0.990613,0.0022272046,0.0011560002,0.0024696959,0.000021002645],"about_ca_topic_score_codex":0.0075146803,"about_ca_topic_score_gemma":0.010285486,"teacher_disagreement_score":0.007853533,"about_ca_system_score_codex":0.0006068153,"about_ca_system_score_gemma":0.00178002,"threshold_uncertainty_score":0.026272714},"labels":[],"label_agreement":null},{"id":"W2410007966","doi":"10.15844/pedneurbriefs-29-11-2","title":"Hereditary Neuropathy with Liability to Pressure Palsies","year":2015,"lang":"en","type":"article","venue":"Pediatric Neurology Briefs","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":6,"is_retracted":false,"has_abstract":true,"route_ca_aff":false,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":true,"ca_institutions":"","funders":"","keywords":"Medicine; Liability; Presentation (obstetrics); Pediatrics; Surgery; Political science; Law","score_opus":0.03517851660747652,"score_gpt":0.24525082141230242,"score_spread":0.21007230480482592,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2410007966","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":[0.99855787,0.0001545293,0.00016267237,0.000037505204,0.0000029065075,0.000029200644,0.00018980222,0.000009561798,0.0008559598],"genre_scores_gemma":[0.9989293,0.00016127272,0.00034949544,0.00004209912,0.0000044693047,0.000016789609,0.00018378269,0.000002965289,0.00030974834],"study_design_codex":"observational","study_design_gemma":"case_report","domain_scores_codex":[0.9994293,0.000048034417,0.00003179954,0.00008024851,0.00014829265,0.00026220563],"domain_scores_gemma":[0.9991923,0.00013910192,0.00018298853,0.000030395153,0.00024819103,0.00020703326],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00033084402,0.00041635716,0.00032816446,0.0008334535,0.0011975848,0.00043918955,0.00039248003,0.00023259457,0.0011141851],"category_scores_gemma":[0.0013106301,0.00019860908,0.00019730406,0.0012931833,0.0007000076,0.00011409562,0.0005421651,0.0003057658,0.00008203447],"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":[0.00012443283,0.00003434061,0.97982866,0.000020133315,0.000027971593,0.010784011,0.00074543443,0.00014009664,0.0014599854,0.000106153864,0.00038238688,0.0063463463],"study_design_scores_gemma":[0.00001718155,0.00008299843,0.990888,0.000012145896,0.00002678306,0.0069116033,0.0006587809,0.0001219992,0.0006576206,0.000032861702,0.0005850767,0.000005079583],"about_ca_topic_score_codex":0.38785627,"about_ca_topic_score_gemma":0.4946413,"teacher_disagreement_score":0.38785627,"about_ca_system_score_codex":0.0029729514,"about_ca_system_score_gemma":0.004193796,"threshold_uncertainty_score":0.7711974},"labels":[],"label_agreement":null},{"id":"W2412454244","doi":"10.1017/s0317167100052550","title":"A Founder Mutation in French-Canadian Families with X-linked Hereditary Neuropathy","year":2001,"lang":"en","type":"article","venue":"Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":6,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":true,"route_about_ca":true,"ca_institutions":"McGill University; Hôpital de l'Enfant-Jésus; Montreal General Hospital; Université Laval","funders":"Medical Research Council; Institut de Réadaptation en Déficience Physique de Québec; Medical Research Council Canada","keywords":"Founder effect; Genetics; Haplotype; Mutation; Biology; Transmembrane domain; Single-strand conformation polymorphism; Gene; Medicine; Genotype","score_opus":0.041575380197550915,"score_gpt":0.2573797824896815,"score_spread":0.2158044022921306,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2412454244","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":[0.9951337,0.0009632245,0.00027503993,0.0002452263,0.000022156328,0.000020576457,0.0003594695,0.000032291606,0.002948292],"genre_scores_gemma":[0.9973247,0.00047146523,0.0005344299,0.00010306899,0.000016663245,0.000008085654,0.00019491985,0.000009662341,0.0013369734],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99964094,0.000039683102,0.000019725454,0.00009267225,0.00010206643,0.000104791325],"domain_scores_gemma":[0.99967337,0.000077016746,0.00007525756,0.000013291668,0.000070473434,0.00009054674],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00022702389,0.0012757089,0.00033684584,0.0013504127,0.0023888552,0.00045817488,0.000518495,0.0008627952,0.005770409],"category_scores_gemma":[0.0009714021,0.00023643926,0.00043274782,0.0011658848,0.0007681451,0.0001419351,0.00057375466,0.00033155287,0.00028686255],"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":[0.0020203432,0.00027942262,0.6066313,0.00046392702,0.00034765655,0.24204838,0.008192654,0.0012074253,0.06439692,0.0027189564,0.0072702016,0.06442279],"study_design_scores_gemma":[0.00018671727,0.0003358801,0.68782806,0.00012726942,0.0004128357,0.28634605,0.0022218938,0.0011400249,0.006493712,0.00041330192,0.014401572,0.000092649825],"about_ca_topic_score_codex":0.5601679,"about_ca_topic_score_gemma":0.62424177,"teacher_disagreement_score":0.4398321,"about_ca_system_score_codex":0.002901539,"about_ca_system_score_gemma":0.0034492447,"threshold_uncertainty_score":0.8848447},"labels":[],"label_agreement":null},{"id":"W2414358872","doi":"10.1017/cjn.2015.42","title":"“Tinkle Tinkle Little Girl, How We Wonder Why You Can’t”: An Unusual AIDP-like Syndrome in a Toddler","year":2015,"lang":"en","type":"article","venue":"Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques","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":true,"route_about_ca":false,"ca_institutions":"Fraser Health; Alberta Children's Hospital","funders":"","keywords":"Toddler; Girl; Wonder; Content (measure theory); Action (physics); Psychology; Developmental psychology; Social psychology; Mathematics; Physics","score_opus":0.09049364458551669,"score_gpt":0.2817897846479041,"score_spread":0.19129614006238743,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2414358872","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":[0.9582812,0.003548103,0.002513274,0.01076695,0.0013118107,0.00031395006,0.000474315,0.00035022057,0.02244013],"genre_scores_gemma":[0.985827,0.0014562582,0.0019774837,0.004427603,0.00045767816,0.000058993308,0.00014863283,0.00008872175,0.005557625],"study_design_codex":"case_report","study_design_gemma":"case_report","domain_scores_codex":[0.99948704,0.000058811795,0.000046468045,0.00016383291,0.00008596073,0.00015786912],"domain_scores_gemma":[0.99937844,0.000111454145,0.00012007714,0.000035771485,0.00005528146,0.00029896162],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00024227073,0.0021077662,0.0014857365,0.0016207587,0.0022902656,0.00096961664,0.0015876224,0.00302236,0.0023376134],"category_scores_gemma":[0.0026012447,0.0008786642,0.0011901412,0.001278251,0.0017973166,0.001579194,0.0015696319,0.0036721812,0.0008251883],"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":[0.000020600311,0.000022772694,0.0033396468,0.00001810414,0.000006073845,0.99471235,0.00025893652,0.000021798434,0.000413221,0.000110047906,0.0004531494,0.0006233206],"study_design_scores_gemma":[0.000006339011,0.00008318583,0.005502528,0.00002050806,0.000008701955,0.9932428,0.00026323795,0.000078207886,0.00011352114,0.00010592925,0.000562666,0.000012346523],"about_ca_topic_score_codex":0.011952501,"about_ca_topic_score_gemma":0.01442505,"teacher_disagreement_score":0.011952501,"about_ca_system_score_codex":0.0015386555,"about_ca_system_score_gemma":0.0009471497,"threshold_uncertainty_score":0.023765862},"labels":[],"label_agreement":null},{"id":"W2417852229","doi":"10.1016/bs.mie.2015.05.004","title":"Functional and Genetic Analysis of Neuronal Isoforms of BPAG1","year":2015,"lang":"en","type":"review","venue":"Methods in enzymology on CD-ROM/Methods in enzymology","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":8,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Ottawa Hospital; University of Ottawa","funders":"Canadian Institutes of Health Research; University of Ottawa","keywords":"Biology; Gene isoform; Microtubule; Cell biology; Chaperone (clinical); Gene; Genetics; Pathology","score_opus":0.2139791962798684,"score_gpt":0.4759999985553044,"score_spread":0.262020802275436,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2417852229","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":[0.004667697,0.98769474,0.00344918,0.0004644421,0.00018161008,0.00001525717,0.00016984309,0.00004270675,0.003314467],"genre_scores_gemma":[0.019510137,0.97271717,0.0037406588,0.00031516302,0.00012857167,0.000025932377,0.0006324525,0.000017491073,0.0029123847],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.9998472,0.000014691816,0.000019108764,0.000037106667,0.00006523761,0.000016742617],"domain_scores_gemma":[0.9998654,0.000053962758,0.000027866268,0.000008575948,0.00003054793,0.000013590134],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00043262364,0.000693166,0.00067970133,0.001108735,0.000115879,0.00059278455,0.0007747038,0.000531721,0.0010111545],"category_scores_gemma":[0.00042512993,0.00021019792,0.0003699404,0.0009971381,0.0005173962,0.00054446334,0.00043352213,0.0011006708,0.0008853387],"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":[0.00015935734,0.00005942608,0.0009437113,0.0063408287,0.000110154564,0.00081021234,0.000057589383,0.0006792612,0.06961021,0.009296101,0.008687321,0.903246],"study_design_scores_gemma":[0.0000362353,0.00011944798,0.004299974,0.001134556,0.0003103219,0.0063208714,0.00007342194,0.00059791264,0.07705403,0.007784105,0.90220857,0.000060475933],"about_ca_topic_score_codex":0.00072451157,"about_ca_topic_score_gemma":0.0007371268,"teacher_disagreement_score":0.001108735,"about_ca_system_score_codex":0.00049515517,"about_ca_system_score_gemma":0.00059309334,"threshold_uncertainty_score":0.0035926104},"labels":[],"label_agreement":null},{"id":"W2423370896","doi":"10.1007/s00381-016-3122-2","title":"Selective dorsal rhizotomy for hereditary spastic paraparesis in children","year":2016,"lang":"en","type":"article","venue":"Child s Nervous System","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":23,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"BC Children's Hospital; University of British Columbia","funders":"","keywords":"Rhizotomy; Spasticity; Medicine; Neurosurgery; Spastic; Dorsum; Cerebral palsy; Physical medicine and rehabilitation; Surgery; Anatomy","score_opus":0.013874214643842664,"score_gpt":0.2246003209428962,"score_spread":0.21072610629905353,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2423370896","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":[0.98861027,0.003516684,0.0010465636,0.00060960517,0.00007194287,0.00002924626,0.00021853202,0.00008713302,0.005810046],"genre_scores_gemma":[0.99624,0.0015924043,0.0009153727,0.00008367423,0.000032668857,0.000016666789,0.000120933066,0.000009056927,0.0009891933],"study_design_codex":"case_report","study_design_gemma":"observational","domain_scores_codex":[0.9999291,0.0000056285467,0.0000070096976,0.000011463546,0.000009880866,0.00003695879],"domain_scores_gemma":[0.9999174,0.000022082633,0.000016396434,0.0000045691245,0.000004647952,0.000034851928],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00007845382,0.00039678544,0.00033557223,0.00034696618,0.0005132383,0.00016759425,0.00027629564,0.00048662702,0.0018596612],"category_scores_gemma":[0.00033086137,0.0001200522,0.000298148,0.00029019904,0.00057409797,0.0002092389,0.0002638542,0.00035430765,0.0002089255],"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":[0.0041135326,0.0007891752,0.19590867,0.0010336766,0.0002960889,0.52901715,0.00051658327,0.0041227993,0.06936224,0.0024309512,0.009329887,0.18307926],"study_design_scores_gemma":[0.00080630794,0.0033940473,0.26361445,0.00021849886,0.00029273477,0.69960964,0.0006498833,0.0028001908,0.021861104,0.0007978206,0.00589743,0.000057897094],"about_ca_topic_score_codex":0.00636563,"about_ca_topic_score_gemma":0.014785824,"teacher_disagreement_score":0.00636563,"about_ca_system_score_codex":0.00055719033,"about_ca_system_score_gemma":0.0012073565,"threshold_uncertainty_score":0.0126571655},"labels":[],"label_agreement":null},{"id":"W2424659274","doi":"10.1017/cjn.2016.161","title":"P.057 Distal hereditary motor neuropathy type I due to the GARS: c.1415A&gt;G, p.His472Arg mutation","year":2016,"lang":"en","type":"article","venue":"Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":0,"is_retracted":false,"has_abstract":true,"route_ca_aff":false,"route_ca_fund":false,"route_ca_venue":true,"route_about_ca":false,"ca_institutions":"","funders":"","keywords":"Weakness; Medicine; Missense mutation; Anatomy; Phenotype; Genetics; Biology; Gene","score_opus":0.03578499785413414,"score_gpt":0.2580973296235719,"score_spread":0.22231233176943777,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2424659274","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":[0.98062503,0.0012827081,0.0011687916,0.0008809445,0.00025932962,0.00007450133,0.0006340713,0.0001489648,0.014925711],"genre_scores_gemma":[0.9949315,0.00033388677,0.000678902,0.00023971134,0.00016174946,0.000014459849,0.00030498338,0.000024943618,0.0033098548],"study_design_codex":"case_report","study_design_gemma":"case_report","domain_scores_codex":[0.99988127,0.000013612712,0.000013701591,0.000032997556,0.000028849681,0.000029523917],"domain_scores_gemma":[0.99973935,0.0000836017,0.00006588165,0.000009151626,0.000021314661,0.00008068209],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00011035622,0.0012819873,0.00034902076,0.0004997403,0.0004965828,0.00031227892,0.0004679695,0.0013059269,0.008937025],"category_scores_gemma":[0.00055832695,0.0001404978,0.00040264716,0.00040507357,0.0006434915,0.0002754243,0.00037904223,0.00049150817,0.0017284269],"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":[0.00054856885,0.00010971314,0.024439985,0.0002042807,0.00006693039,0.92945474,0.0003368151,0.00030695339,0.031382635,0.0010861732,0.0020953924,0.009967851],"study_design_scores_gemma":[0.00018531336,0.000965962,0.09799331,0.00016504007,0.0001781446,0.8668748,0.00045939544,0.0016552247,0.021869995,0.001696453,0.007903902,0.000052459498],"about_ca_topic_score_codex":0.0022443666,"about_ca_topic_score_gemma":0.001341206,"teacher_disagreement_score":0.008937025,"about_ca_system_score_codex":0.00032976017,"about_ca_system_score_gemma":0.00038942505,"threshold_uncertainty_score":0.029897332},"labels":[],"label_agreement":null},{"id":"W2491975933","doi":"10.1212/wnl.86.16_supplement.p5.075","title":"Hereditary Spastic Paraplegia Type 4 (SPG4): A Clinico-Genetic Study in a Large Cohort of Patients with Spastic Paraplegia (P5.075)","year":2016,"lang":"en","type":"article","venue":"Neurology","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":false,"ca_institutions":"Toronto Western Hospital; University of Toronto","funders":"","keywords":"Hereditary spastic paraplegia; Paraplegia; Medicine; Spastic; Cohort; Pediatrics; Physical therapy; Internal medicine; Cerebral palsy; Genetics; Psychiatry; Spinal cord; Biology; Phenotype","score_opus":0.021982356926953477,"score_gpt":0.26543507169464114,"score_spread":0.24345271476768768,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2491975933","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":[0.9996791,0.000058708487,0.000044712542,0.000010016385,0.000002186738,0.000007006729,0.00007391104,0.0000017779611,0.00012270312],"genre_scores_gemma":[0.99949014,0.00006564343,0.00006232379,0.000017763889,0.000011757674,0.000010883885,0.00024193415,0.000002198757,0.00009727911],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9995752,0.00009232118,0.00003549441,0.0001659931,0.00007114602,0.00005979771],"domain_scores_gemma":[0.9995528,0.00007374387,0.00012836786,0.000046539844,0.00005448999,0.00014408761],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00043043788,0.0006542581,0.00054568995,0.0011063436,0.001137592,0.00054607476,0.00034835775,0.0005890869,0.0017730278],"category_scores_gemma":[0.0013007289,0.00043693042,0.0003973502,0.0009901178,0.0004486166,0.000404051,0.00061817234,0.0003992797,0.0004043373],"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":[0.00016909423,0.000082141676,0.9952083,0.000007667433,0.00006354546,0.0017933302,0.00020149554,0.000024130477,0.0012609618,0.000017488539,0.00009045483,0.0010813854],"study_design_scores_gemma":[0.000026580357,0.00024689775,0.9921881,0.0000070619526,0.000044945027,0.006729768,0.00031015766,0.00011940127,0.00009455505,0.000022347776,0.00020436905,0.0000058034057],"about_ca_topic_score_codex":0.0030570463,"about_ca_topic_score_gemma":0.002520128,"teacher_disagreement_score":0.0030570463,"about_ca_system_score_codex":0.00021612161,"about_ca_system_score_gemma":0.0003005983,"threshold_uncertainty_score":0.0060784817},"labels":[],"label_agreement":null},{"id":"W2511959561","doi":"10.1002/ajmg.a.37929","title":"Phenotypic evolution of UNC80 loss of function","year":2016,"lang":"en","type":"article","venue":"American Journal of Medical Genetics Part A","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":19,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Child and Family Research Institute; University of British Columbia","funders":"National Human Genome Research Institute; Common Fund; National Institutes of Health; Child and Family Research Institute","keywords":"Failure to thrive; Loss function; Exome sequencing; Nonsense; Genetics; Phenotype; Gain of function; Biology; Nonsense mutation; Hereditary spastic paraplegia; Mutation; Gene; Missense mutation","score_opus":0.021489986066534062,"score_gpt":0.2665032840377287,"score_spread":0.24501329797119464,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2511959561","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":[0.99246275,0.00033125968,0.0012157992,0.00024938208,0.000029939476,0.00002197208,0.00028275538,0.000105834355,0.005300291],"genre_scores_gemma":[0.9965745,0.00019841638,0.0009175197,0.00015062094,0.000014926028,0.000012678724,0.00019604567,0.00005104159,0.0018843508],"study_design_codex":"case_report","study_design_gemma":"observational","domain_scores_codex":[0.9998079,0.000019318599,0.000017588645,0.00006150385,0.000057061607,0.00003653723],"domain_scores_gemma":[0.999814,0.000037465852,0.000045035576,0.00001794661,0.000026485557,0.00005912345],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00013228104,0.0008375587,0.0003082887,0.0007356156,0.0005169171,0.00034742398,0.0003807496,0.0006485988,0.002186989],"category_scores_gemma":[0.0008969637,0.00016932774,0.00023573989,0.00034355326,0.0005038009,0.00027611316,0.0007876202,0.00061149965,0.0007223912],"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":[0.00059910177,0.0002301818,0.061055034,0.00008135799,0.00008407106,0.51129645,0.0011248703,0.00073674927,0.38333786,0.0013803409,0.0025564586,0.037517596],"study_design_scores_gemma":[0.00003349496,0.0003028184,0.13282037,0.000031302487,0.000069008165,0.8321403,0.00031028717,0.0013457556,0.02791214,0.0006279009,0.0043674335,0.000039232316],"about_ca_topic_score_codex":0.0012897311,"about_ca_topic_score_gemma":0.0012897617,"teacher_disagreement_score":0.002186989,"about_ca_system_score_codex":0.00031116622,"about_ca_system_score_gemma":0.00026335457,"threshold_uncertainty_score":0.007316172},"labels":[],"label_agreement":null},{"id":"W2521832260","doi":"10.1016/j.rehab.2016.07.134","title":"Motor, cognitive and psychosocial impacts of an adapted dance program among children with Charcot-Marie-Tooth disease: An exploratory study","year":2016,"lang":"en","type":"article","venue":"Annals of Physical and Rehabilitation Medicine","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":2,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Université du Québec à Montréal","funders":"","keywords":"Psychosocial; Dance; Tooth disease; Physical medicine and rehabilitation; Cognition; Psychology; Disease; Motor skill; Physical therapy; Exploratory research; Medicine; Gerontology; Developmental psychology; Psychiatry; Sociology","score_opus":0.03360602797276978,"score_gpt":0.33860441677951847,"score_spread":0.3049983888067487,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2521832260","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":[0.99979526,0.000021814623,0.000008543845,0.000005779159,0.0000012056873,0.0000500016,0.000023639252,5.626422e-7,0.00009318448],"genre_scores_gemma":[0.99908435,0.00010728354,0.0001475091,0.00002887847,0.0000087573835,0.0002117172,0.00011516465,0.0000010934339,0.0002952365],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9993431,0.00019667714,0.00004889023,0.00009698257,0.000094414245,0.0002199604],"domain_scores_gemma":[0.99950385,0.00012296942,0.00011047619,0.000037078367,0.00006231526,0.00016329222],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00075565075,0.0008027347,0.0008085096,0.0007676168,0.0015028071,0.0005281699,0.0004766908,0.00085149263,0.0010289125],"category_scores_gemma":[0.001256861,0.0003868197,0.0012123106,0.000728755,0.0006566231,0.0004800187,0.0007162259,0.000847045,0.00017063165],"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":[0.014350207,0.14353803,0.78032005,0.00045629806,0.00073028967,0.0029634472,0.010633919,0.000668694,0.0059255688,0.00013674967,0.0002694387,0.040007263],"study_design_scores_gemma":[0.0013326614,0.051589623,0.9376397,0.00003292215,0.0003167982,0.00042916663,0.007531347,0.00020427673,0.00046292192,0.000041757445,0.00037699548,0.00004180119],"about_ca_topic_score_codex":0.014874294,"about_ca_topic_score_gemma":0.026524898,"teacher_disagreement_score":0.014874294,"about_ca_system_score_codex":0.0013243563,"about_ca_system_score_gemma":0.0011306249,"threshold_uncertainty_score":0.029575408},"labels":[],"label_agreement":null},{"id":"W2524136143","doi":"10.2460/ajvr.77.10.1114","title":"Evaluation of the dynactin 1 gene in Leonbergers and Labrador Retrievers with laryngeal paralysis","year":2016,"lang":"en","type":"article","venue":"American Journal of Veterinary Research","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":2,"is_retracted":false,"has_abstract":true,"route_ca_aff":false,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":true,"ca_institutions":"","funders":"","keywords":"Exon; Biology; Gene; Genetics; Coding region; Labrador Retriever; Medicine; Pathology","score_opus":0.17948508705219987,"score_gpt":0.3981230149229154,"score_spread":0.21863792787071554,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2524136143","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":[0.99966383,0.000074816955,0.000038620932,0.0000058047394,0.0000011892907,0.0000041748294,0.000030347817,0.0000021148674,0.00017914685],"genre_scores_gemma":[0.9992674,0.00007160645,0.00015981102,0.00002608184,0.0000042260317,0.0000061273336,0.00017891654,0.0000027895758,0.00028305917],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9996834,0.000041632553,0.000034161978,0.000089459885,0.00008977748,0.00006160484],"domain_scores_gemma":[0.999718,0.000057258057,0.000121908095,0.000011938059,0.000033208522,0.00005759497],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00035933973,0.00039255802,0.00029472634,0.00085767143,0.0002953612,0.0002649538,0.00023248458,0.0005401722,0.0013228196],"category_scores_gemma":[0.00087328407,0.00018063669,0.0001891508,0.0002544573,0.0005166248,0.00022099288,0.00021324592,0.0001359273,0.00027018713],"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":[0.0011820522,0.00019774535,0.8074061,0.00012015614,0.00011975929,0.014412888,0.0012872452,0.00030577538,0.16495624,0.00012122865,0.00021824049,0.0096726185],"study_design_scores_gemma":[0.000027773758,0.0007050524,0.9779825,0.000016362595,0.000042814452,0.016225053,0.0004906537,0.00031576338,0.003654162,0.00003165855,0.0005001874,0.000007960252],"about_ca_topic_score_codex":0.0022504271,"about_ca_topic_score_gemma":0.004426457,"teacher_disagreement_score":0.0022504271,"about_ca_system_score_codex":0.00037923755,"about_ca_system_score_gemma":0.00013238199,"threshold_uncertainty_score":0.00447464},"labels":[],"label_agreement":null},{"id":"W2527001044","doi":"10.1212/wnl.86.16_supplement.p6.255","title":"Electrophysiological Characterization of Hereditary Neuropathy with Liability to Pressure Palsies (HNPP) (P6.255)","year":2016,"lang":"en","type":"article","venue":"Neurology","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":"University Hospital; London Health Sciences Centre; Western University","funders":"","keywords":"Medicine; Liability; Political science; Law","score_opus":0.013919404732615449,"score_gpt":0.2185610519095305,"score_spread":0.20464164717691508,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2527001044","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":[0.9993079,0.00015954157,0.00014102782,0.0000061525557,0.0000014326725,0.000005039988,0.00012212998,0.0000031412194,0.00025360327],"genre_scores_gemma":[0.99947554,0.00007004717,0.00010382003,0.000007698222,0.0000031398356,0.0000035031937,0.00023638918,0.0000013503388,0.00009862233],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99984944,0.000019983716,0.000023698274,0.000046570975,0.000037469395,0.0000228692],"domain_scores_gemma":[0.999597,0.000089188594,0.0001492133,0.000023582195,0.00006206609,0.000078999845],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00029319723,0.00024705686,0.00019858558,0.00055397965,0.0001831108,0.00023822715,0.00015882541,0.00019152314,0.0015232895],"category_scores_gemma":[0.0009947285,0.00007787267,0.00013592638,0.00026417084,0.00022774453,0.00017857719,0.00025487467,0.00011223645,0.00025535314],"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":[0.00014327421,0.000027103146,0.9812924,0.000029237848,0.000025885296,0.0060988218,0.00009623747,0.000092217626,0.008177611,0.000021847489,0.0000800408,0.003915159],"study_design_scores_gemma":[0.000004804156,0.00017812372,0.98058414,0.000007077921,0.00001305722,0.018317716,0.0000885388,0.000095933414,0.000574559,0.000011874445,0.00012186352,0.0000023589819],"about_ca_topic_score_codex":0.001479513,"about_ca_topic_score_gemma":0.0016879315,"teacher_disagreement_score":0.0015232895,"about_ca_system_score_codex":0.00014976913,"about_ca_system_score_gemma":0.00017702511,"threshold_uncertainty_score":0.005095899},"labels":[],"label_agreement":null},{"id":"W2532482249","doi":"10.1016/j.ijoa.2016.10.005","title":"Anesthetic considerations in a parturient with congenital insensitivity to pain with anhidrosis","year":2016,"lang":"en","type":"article","venue":"International Journal of Obstetric Anesthesia","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":5,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"London Health Sciences Centre","funders":"","keywords":"Medicine; Anesthesia; Anesthetic; Bradycardia; Cesarean delivery; Anhidrosis; Local anesthetic; Surgery; Pregnancy; Heart rate; Internal medicine; Blood pressure","score_opus":0.024546356683279376,"score_gpt":0.24363800994219084,"score_spread":0.21909165325891147,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2532482249","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":[0.8609009,0.017134104,0.0039316923,0.07124998,0.0033096175,0.00041832015,0.0004929977,0.00050784135,0.042054497],"genre_scores_gemma":[0.98087925,0.004231439,0.002867164,0.005567819,0.0030187194,0.000040994622,0.00014076247,0.00006118897,0.0031927256],"study_design_codex":"case_report","study_design_gemma":"case_report","domain_scores_codex":[0.99945325,0.000055654895,0.00008619144,0.000080674465,0.000115523915,0.00020865303],"domain_scores_gemma":[0.9983948,0.00043040104,0.00030615242,0.00003992202,0.00008378175,0.0007449383],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0003955192,0.0016547344,0.0011084487,0.0028523307,0.0029430618,0.0017081983,0.0017037798,0.008465056,0.004605006],"category_scores_gemma":[0.0043684524,0.0008069336,0.0011402625,0.00090593455,0.0019457383,0.00144228,0.0013284215,0.0060046143,0.00084813737],"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":[0.000029093833,0.00002278778,0.0026363644,0.000013729304,0.000004412922,0.9957397,0.000053505115,0.00007387572,0.0003132255,0.00012290583,0.00036493043,0.00062557455],"study_design_scores_gemma":[0.000015462296,0.00015945737,0.005577033,0.00004645566,0.000016006583,0.99170387,0.00046215652,0.00044723827,0.00032941203,0.00037419083,0.0008534748,0.000015192843],"about_ca_topic_score_codex":0.0044040396,"about_ca_topic_score_gemma":0.0082635945,"teacher_disagreement_score":0.008465056,"about_ca_system_score_codex":0.002210467,"about_ca_system_score_gemma":0.001967472,"threshold_uncertainty_score":0.01603812},"labels":[],"label_agreement":null},{"id":"W2541571632","doi":"10.1212/wnl.86.16_supplement.p5.100","title":"Diagnostic Neurosonography in Mouse Models of Demyelinating Charcot-Marie-Tooth Diseae Type 1A (P5.100)","year":2016,"lang":"en","type":"article","venue":"Neurology","topic":"Hereditary Neurological Disorders","field":"Neuroscience","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; Tooth disease; Pathology; Disease","score_opus":0.04016689860019986,"score_gpt":0.2601786279396724,"score_spread":0.22001172933947252,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2541571632","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":[0.98950994,0.0030140162,0.0052850232,0.00013925396,0.00007228335,0.00011849591,0.00055952533,0.00024471385,0.0010567772],"genre_scores_gemma":[0.98250383,0.0026769158,0.009356573,0.00011968242,0.000019809459,0.0003875485,0.0011140468,0.00005905851,0.003762586],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9993444,0.00011472167,0.00005543801,0.00017661431,0.00022424385,0.00008461595],"domain_scores_gemma":[0.99939406,0.00006486048,0.00027923335,0.000038309787,0.00006561777,0.00015788937],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0006479983,0.0008803785,0.00045527943,0.002066535,0.00025592762,0.00038668056,0.00035847438,0.00075834116,0.0016725033],"category_scores_gemma":[0.00031336988,0.00027177812,0.0003571238,0.00048632495,0.00065839145,0.00047379287,0.00031586725,0.0008192085,0.00030729568],"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":[0.0003795758,0.00014923704,0.00067947904,0.0000728288,0.000013952518,0.00016720466,0.00003478816,0.000048903337,0.99678564,0.000048295355,0.000051330768,0.0015689197],"study_design_scores_gemma":[0.00013993723,0.007177739,0.034810968,0.00009028618,0.00017713712,0.002700166,0.00026950438,0.0018094109,0.9503177,0.00013056527,0.0023453166,0.0000313562],"about_ca_topic_score_codex":0.00072677905,"about_ca_topic_score_gemma":0.0014815517,"teacher_disagreement_score":0.002066535,"about_ca_system_score_codex":0.0004264702,"about_ca_system_score_gemma":0.00026462635,"threshold_uncertainty_score":0.005595088},"labels":[],"label_agreement":null},{"id":"W2552466405","doi":"10.1007/978-3-319-43169-7_85","title":"Charcot–Marie–Tooth Disease and Regional Anesthesia: Is Perioperative Neuraxial Analgesia Really Contraindicated?","year":2016,"lang":"en","type":"book-chapter","venue":"","topic":"Hereditary Neurological Disorders","field":"Neuroscience","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":"Kimberly-Clark (Canada)","funders":"","keywords":"Medicine; Perioperative; Bowel obstruction; Surgery; Abdominal pain; Anesthesia; General surgery","score_opus":0.03618261497768858,"score_gpt":0.24325808696418277,"score_spread":0.2070754719864942,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2552466405","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":[0.006638956,0.5302377,0.0042868364,0.1476581,0.01786202,0.000030369114,0.00023814462,0.00014802157,0.29289994],"genre_scores_gemma":[0.08051614,0.4784793,0.00983772,0.10145844,0.037681248,0.000109010616,0.0004920849,0.0002101449,0.2912159],"study_design_codex":"not_applicable","study_design_gemma":"observational","domain_scores_codex":[0.9998292,0.000038395978,0.00001877269,0.000023317514,0.00006529321,0.000024948118],"domain_scores_gemma":[0.99945205,0.00040824403,0.00003840423,0.000013023994,0.000042570664,0.0000457568],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00048275533,0.00049773796,0.00061289594,0.00045830786,0.00033281045,0.0009264974,0.0006819964,0.003022768,0.010381968],"category_scores_gemma":[0.0020105077,0.00023093152,0.00028805557,0.0003595258,0.0012747148,0.0017456149,0.0005094694,0.0032328886,0.00329454],"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":[0.00013531554,0.00008328094,0.0010372218,0.00066443055,0.000029377228,0.014095443,0.00044454384,0.00029703893,0.0013148356,0.059878502,0.58320177,0.3388183],"study_design_scores_gemma":[0.0000376443,0.000054022978,0.0018682188,0.0014256581,0.000030137993,0.042881854,0.00033190133,0.0001830403,0.00033005813,0.047827538,0.9049953,0.000034654957],"about_ca_topic_score_codex":0.0018786686,"about_ca_topic_score_gemma":0.003223595,"teacher_disagreement_score":0.010381968,"about_ca_system_score_codex":0.00079622027,"about_ca_system_score_gemma":0.001003958,"threshold_uncertainty_score":0.03473115},"labels":[],"label_agreement":null},{"id":"W2553213529","doi":"10.71781/27425","title":"A Québec mystery unveiled : the quest to understand hereditary sensory and autonomic neuropathy type 2","year":2007,"lang":"en","type":"dissertation","venue":"Papyrus : Institutional Repository (Université de Montréal)","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":0,"is_retracted":false,"has_abstract":false,"route_ca_aff":false,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":true,"ca_institutions":"","funders":"","keywords":"Sensory system; Sensory neuropathy; Neuroscience; Medicine; Biology; Internal medicine","score_opus":0.013557863879218892,"score_gpt":0.2027387670937883,"score_spread":0.1891809032145694,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2553213529","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":[0.04455476,0.12054936,0.0016993113,0.58693266,0.004593813,0.0000718819,0.0032217922,0.00016822548,0.23820825],"genre_scores_gemma":[0.37631744,0.13925342,0.0046817474,0.056437608,0.002147997,0.000099398836,0.0017681154,0.00021653682,0.4190777],"study_design_codex":"not_applicable","study_design_gemma":"observational","domain_scores_codex":[0.9995517,0.000081295904,0.000012503184,0.000046878606,0.00015356748,0.00015397869],"domain_scores_gemma":[0.9989267,0.00013888058,0.000048793438,0.00004206883,0.00063110975,0.00021233525],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.001032085,0.00035823626,0.0003741807,0.0010333182,0.00463364,0.0024250378,0.00059077656,0.0010436713,0.016208086],"category_scores_gemma":[0.0018987572,0.00017705956,0.00023932013,0.00156349,0.0021023294,0.0013796181,0.00081318367,0.0022863399,0.0009964885],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":true,"about_ca_topic_consensus":true,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00012470952,0.000069445596,0.011096184,0.0003048016,0.000053708347,0.001215205,0.0066586477,0.00071203156,0.0009502717,0.09996377,0.7192952,0.15955593],"study_design_scores_gemma":[0.00003014185,0.00003109308,0.039679613,0.00064198574,0.000032895347,0.00062601257,0.006325241,0.00062664575,0.0005509415,0.018850593,0.9325556,0.00004922477],"about_ca_topic_score_codex":0.9705015,"about_ca_topic_score_gemma":0.98994815,"teacher_disagreement_score":0.034721486,"about_ca_system_score_codex":0.034721486,"about_ca_system_score_gemma":0.054450702,"threshold_uncertainty_score":0.2519232},"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":"W2561067840","doi":"10.1371/journal.pgen.1006482","title":"A Point Mutation in a lincRNA Upstream of GDNF Is Associated to a Canine Insensitivity to Pain: A Spontaneous Model for Human Sensory Neuropathies","year":2016,"lang":"en","type":"article","venue":"PLoS Genetics","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":56,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Centre Hospitalier Universitaire Sainte-Justine; Université de Montréal","funders":"Région Bretagne; Agence Nationale de la Recherche; Centre National de la Recherche Scientifique; Conseil Régional de Bretagne; European Commission; Companion Animal Health Fund","keywords":"Biology; Genetics; Glial cell line-derived neurotrophic factor; Locus (genetics); Genome-wide association study; Point mutation; Gene; Genotype; Mutation; Single-nucleotide polymorphism; Neurotrophic factors","score_opus":0.06624632392157617,"score_gpt":0.2743137880245348,"score_spread":0.20806746410295865,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2561067840","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":[0.9962005,0.00025629363,0.0018574307,0.0000996035,0.000035769175,0.000059068298,0.0006929854,0.000067276684,0.00073100894],"genre_scores_gemma":[0.99568653,0.00015894687,0.0016440133,0.00008005365,0.000016836759,0.00005381015,0.0011498393,0.000031735246,0.0011782515],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.999811,0.00003683462,0.00001908478,0.00006871461,0.000039856903,0.000024662095],"domain_scores_gemma":[0.9998729,0.00003333187,0.0000368589,0.000013187317,0.00001003088,0.000033746586],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00013889243,0.00030689602,0.00023991826,0.00046250064,0.00024845763,0.00016119974,0.00023258191,0.0003766117,0.002194195],"category_scores_gemma":[0.00024447302,0.00014685637,0.0002615781,0.00031038496,0.00033514845,0.00007279142,0.00030035424,0.00040601325,0.00027928414],"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":[0.00086298794,0.00019434726,0.003677602,0.000103884326,0.00005121201,0.0033143177,0.00011819682,0.0001939355,0.9871818,0.00040047482,0.00045174683,0.0034495445],"study_design_scores_gemma":[0.0016500107,0.0064493176,0.41134837,0.000150966,0.0006076561,0.067520805,0.0005917857,0.01392207,0.45587993,0.0011554193,0.040604986,0.000118677795],"about_ca_topic_score_codex":0.0013691266,"about_ca_topic_score_gemma":0.0023615328,"teacher_disagreement_score":0.002194195,"about_ca_system_score_codex":0.00026278343,"about_ca_system_score_gemma":0.00013575242,"threshold_uncertainty_score":0.007340312},"labels":[],"label_agreement":null},{"id":"W2567485069","doi":"10.1002/ana.24855","title":"<scp><i>KCNA2</i></scp> mutations are rare in hereditary spastic paraplegia","year":2016,"lang":"en","type":"letter","venue":"Annals of Neurology","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":0,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Université Laval; University of Alberta; Montreal Neurological Institute and Hospital; SickKids Foundation; University of Toronto; McGill University; Hospital for Sick Children","funders":"Canadian Institutes of Health Research","keywords":"Medicine; Neurology; Hereditary spastic paraplegia; Family medicine; Library science; Psychiatry; Genetics","score_opus":0.09090006987553093,"score_gpt":0.30198354704115443,"score_spread":0.2110834771656235,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2567485069","genre_codex":"commentary","genre_gemma":"editorial","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"editorial","genre_consensus":null,"domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.2440049,0.01640646,0.0020158459,0.5436964,0.018800894,0.00012325891,0.0009221587,0.0007893579,0.17324074],"genre_scores_gemma":[0.8264459,0.009470901,0.0013509445,0.07377968,0.032991488,0.000052028416,0.0003834274,0.00018643167,0.05533932],"study_design_codex":"case_report","study_design_gemma":"observational","domain_scores_codex":[0.9995436,0.000066537345,0.000059339254,0.00008955561,0.00012513099,0.00011585191],"domain_scores_gemma":[0.9988418,0.00042313486,0.00022261773,0.00008028765,0.00019707778,0.00023510764],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00037904113,0.00069219957,0.00081298733,0.000980928,0.0018240355,0.001034828,0.0007239256,0.007205311,0.0076068593],"category_scores_gemma":[0.0042615477,0.00030223944,0.00046752207,0.00071592594,0.0015853137,0.0011926095,0.0004753103,0.0043501696,0.0051100603],"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":[0.00020512016,0.00008925521,0.014868513,0.00015109591,0.00003499397,0.809665,0.00039189818,0.00021630179,0.0017225316,0.00315192,0.15002069,0.019482689],"study_design_scores_gemma":[0.00008504306,0.0001072581,0.0138043985,0.00031338597,0.000049630256,0.9298046,0.0002827635,0.00087710697,0.0010181462,0.0055305283,0.048081957,0.00004519869],"about_ca_topic_score_codex":0.0036182662,"about_ca_topic_score_gemma":0.0058282455,"teacher_disagreement_score":0.0076068593,"about_ca_system_score_codex":0.0017024113,"about_ca_system_score_gemma":0.0007261197,"threshold_uncertainty_score":0.025447488},"labels":[],"label_agreement":null},{"id":"W2568127139","doi":"10.1093/brain/aww318","title":"A mutation of<i>EPT1 (SELENOI)</i>underlies a new disorder of Kennedy pathway phospholipid biosynthesis","year":2016,"lang":"en","type":"article","venue":"Brain","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":78,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Dalhousie University","funders":"Biomedical Research Council; National Medical Research Council; Medical Research Council; Ministry of Education, India; National University of Singapore; Agency for Science, Technology and Research; National Research Foundation; Newlife the Charity for Disabled Children","keywords":"Phosphatidylethanolamine; Hereditary spastic paraplegia; Glycerophospholipid; Biology; Mutation; Biochemistry; Biosynthesis; Gene; Phosphatidylcholine; Phospholipid; Genetics; Phenotype","score_opus":0.02499178398977982,"score_gpt":0.23480145795222407,"score_spread":0.20980967396244424,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2568127139","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":[0.99126136,0.0012771825,0.0042798114,0.00022092066,0.000041835963,0.00003456561,0.00041864524,0.000147384,0.0023182156],"genre_scores_gemma":[0.9955323,0.00093155605,0.0017520279,0.00005683162,0.000032489483,0.000011689534,0.0003558958,0.000018954888,0.0013081849],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9999001,0.000012858446,0.000013251594,0.00003704396,0.000020047684,0.00001667541],"domain_scores_gemma":[0.99987423,0.000029430325,0.000055167602,0.000008022579,0.000009902483,0.000023242636],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.000094431365,0.0009927579,0.00034356798,0.0004982216,0.00036200273,0.00020672423,0.00023564797,0.0005570249,0.0014303201],"category_scores_gemma":[0.0002165868,0.0001073246,0.00021662543,0.00026495254,0.0005695359,0.00015629323,0.000488398,0.00039880627,0.00031654132],"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":[0.0011462768,0.00012922497,0.023531478,0.00026592377,0.00012452701,0.19679515,0.00042293398,0.00048928946,0.7461422,0.00220747,0.0011197528,0.027625775],"study_design_scores_gemma":[0.000070641756,0.0008425128,0.10684107,0.00008879012,0.0002313553,0.5807576,0.00027623112,0.0018231141,0.29257244,0.0010672383,0.0153782815,0.000050720744],"about_ca_topic_score_codex":0.0007085507,"about_ca_topic_score_gemma":0.0007230368,"teacher_disagreement_score":0.0014303201,"about_ca_system_score_codex":0.00019404269,"about_ca_system_score_gemma":0.00020393675,"threshold_uncertainty_score":0.0047849417},"labels":[],"label_agreement":null},{"id":"W2574515614","doi":"10.1017/cjn.2016.427","title":"Concurrent Dawson’s Fingers and Area Postrema Lesion in a Mixed Neuroimmune Disorder","year":2017,"lang":"en","type":"letter","venue":"Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":2,"is_retracted":false,"has_abstract":true,"route_ca_aff":false,"route_ca_fund":false,"route_ca_venue":true,"route_about_ca":false,"ca_institutions":"","funders":"","keywords":"Area postrema; Lesion; Medicine; Neuroscience; Psychology; Pathology; Internal medicine; Central nervous system","score_opus":0.08160540721586898,"score_gpt":0.2893990991118791,"score_spread":0.20779369189601013,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2574515614","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":[0.8313763,0.0070049907,0.0031416335,0.04658945,0.0036824534,0.00030649616,0.0007078011,0.00048363802,0.1067072],"genre_scores_gemma":[0.98454237,0.0010858037,0.0009343446,0.004706557,0.0031783986,0.000033926364,0.00009901947,0.00004467497,0.0053748847],"study_design_codex":"case_report","study_design_gemma":"case_report","domain_scores_codex":[0.99920076,0.00009001665,0.000085563035,0.00021917615,0.00016564713,0.0002388419],"domain_scores_gemma":[0.99800414,0.0008772926,0.00023507183,0.00015972229,0.0001358167,0.0005878514],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0005458364,0.0017551181,0.0012822663,0.0023959284,0.003292801,0.0017894309,0.0018719246,0.008441327,0.0057606776],"category_scores_gemma":[0.0045810645,0.0008443422,0.00082850026,0.0018180211,0.002700308,0.0024072358,0.0011338417,0.0059093605,0.0012294364],"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":[0.000063785286,0.00005233731,0.0028609575,0.000026776212,0.000010743943,0.9933422,0.00007528699,0.000060684783,0.00037774738,0.00071846956,0.0012345323,0.0011764591],"study_design_scores_gemma":[0.00006603792,0.00007021807,0.0061280937,0.000044080523,0.00002379141,0.99002224,0.00017355588,0.00046601493,0.0003162296,0.0013691809,0.0013009891,0.000019580808],"about_ca_topic_score_codex":0.008089444,"about_ca_topic_score_gemma":0.0118827075,"teacher_disagreement_score":0.008441327,"about_ca_system_score_codex":0.0043478077,"about_ca_system_score_gemma":0.0020892057,"threshold_uncertainty_score":0.03154564},"labels":[],"label_agreement":null},{"id":"W2578320483","doi":"10.1212/wnl.86.16_supplement.s44.002","title":"Identification of ALS5/SPG11/ <i>KIAA1840</i> Mutations in Patients with Autosomal Recessive Form of Charcot-Marie-Tooth Disease Type 2 (S44.002)","year":2016,"lang":"en","type":"article","venue":"Neurology","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":"Occupational Cancer Research Centre; University of Toronto","funders":"","keywords":"Medicine; Tooth disease; Genetics; Disease; Internal medicine; Biology","score_opus":0.01358010008997481,"score_gpt":0.24073132318471452,"score_spread":0.2271512230947397,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2578320483","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":[0.9997316,0.00004047111,0.000041132556,0.000008135547,0.0000010599008,0.0000057655134,0.00004095766,0.000003138541,0.00012767094],"genre_scores_gemma":[0.99959296,0.000024671559,0.0001325764,0.000021123218,0.000003082779,0.0000047041294,0.00009999751,0.0000019038457,0.0001188668],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99976116,0.00003960734,0.000027552405,0.00008158239,0.000046063953,0.000044020515],"domain_scores_gemma":[0.99979,0.000034817956,0.00007916187,0.0000087507415,0.000030359726,0.000056848483],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00022366212,0.0005367786,0.00022786987,0.0009278676,0.000575636,0.00032939474,0.00023468763,0.00038363267,0.0019187132],"category_scores_gemma":[0.0006329387,0.0001803486,0.00018711125,0.0005178973,0.00029042322,0.00013048766,0.00027145984,0.00016114303,0.0002448047],"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":[0.00032387144,0.00012348701,0.9615586,0.000034293298,0.000056918856,0.00951932,0.00061955384,0.00010944519,0.020661637,0.000039226492,0.0002286328,0.006724998],"study_design_scores_gemma":[0.000045154608,0.00038128605,0.98180044,0.000014107693,0.000056165376,0.014668686,0.0003387907,0.00021946813,0.0018935102,0.000035030775,0.0005395526,0.000007785527],"about_ca_topic_score_codex":0.0033739996,"about_ca_topic_score_gemma":0.0036224339,"teacher_disagreement_score":0.0033739996,"about_ca_system_score_codex":0.00025724596,"about_ca_system_score_gemma":0.00021832115,"threshold_uncertainty_score":0.006708741},"labels":[],"label_agreement":null},{"id":"W2582026000","doi":"10.1111/apa.13750","title":"Exercise and the multidisciplinary holistic approach to adolescent dysautonomia","year":2017,"lang":"en","type":"article","venue":"Acta Paediatrica","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":11,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Simon Fraser University; BC Children's Hospital; University of British Columbia","funders":"","keywords":"Medicine; Psychosocial; Physical therapy; Quality of life (healthcare); Dysautonomia; Multidisciplinary approach; Pediatrics; Internal medicine; Disease; Psychiatry","score_opus":0.05531687014951733,"score_gpt":0.2856928567772082,"score_spread":0.23037598662769085,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2582026000","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":[0.92251575,0.049792074,0.0020733206,0.010689491,0.00077249715,0.00019958439,0.000043943084,0.000028024591,0.01388533],"genre_scores_gemma":[0.97662055,0.015544972,0.004629672,0.0011647394,0.0003494458,0.00017311645,0.000035164336,0.0000037623765,0.0014786148],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.99968815,0.00018302521,0.000015980093,0.00002425679,0.00005370965,0.000034833007],"domain_scores_gemma":[0.9996865,0.00007632881,0.00005733264,0.000007841208,0.000026518219,0.000145441],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00056977646,0.00015721214,0.00026335253,0.00025631808,0.00025347204,0.00036923026,0.00020512675,0.00033173405,0.0016897854],"category_scores_gemma":[0.0010784577,0.000069103975,0.00022971381,0.00012701735,0.00022396512,0.0002570111,0.0007981677,0.000619165,0.00010567365],"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":[0.001099609,0.005393984,0.11142527,0.0033494034,0.00042223508,0.0010201616,0.0017629297,0.0008611514,0.006781016,0.0014266869,0.004981709,0.86147594],"study_design_scores_gemma":[0.001425594,0.0123385,0.9348727,0.005049106,0.0005434734,0.005294068,0.0050699725,0.0022448283,0.0016951206,0.002514218,0.028909717,0.000042623207],"about_ca_topic_score_codex":0.00078623096,"about_ca_topic_score_gemma":0.0039443932,"teacher_disagreement_score":0.0016897854,"about_ca_system_score_codex":0.00027476018,"about_ca_system_score_gemma":0.0007923662,"threshold_uncertainty_score":0.0056529045},"labels":[],"label_agreement":null},{"id":"W2584904213","doi":"10.1016/j.jocd.2017.01.002","title":"Genetic Polymorphisms in the ESR1 and VDR Genes Do Not Correlate With Osteoporosis in Patients With Familial Dysautonomia","year":2017,"lang":"en","type":"article","venue":"Journal of Clinical Densitometry","topic":"Hereditary Neurological Disorders","field":"Neuroscience","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":"McGill University","funders":"","keywords":"Calcitriol receptor; Osteoporosis; Medicine; Familial dysautonomia; Bone mineral; Internal medicine; Vitamin D and neurology; Estrogen receptor alpha; Endocrinology; Polymorphism (computer science); Bone density; Genotype; Estrogen receptor; Genetics; Gene; Biology","score_opus":0.043636490748694856,"score_gpt":0.3166419352811769,"score_spread":0.27300544453248204,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2584904213","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":[0.9989818,0.00032037054,0.000049141145,0.00004952151,0.000010556748,0.00000220939,0.00007037151,0.000004402214,0.0005114439],"genre_scores_gemma":[0.9997147,0.00006129974,0.00003400965,0.000016459673,0.0000112876305,0.000001688065,0.000060681563,0.0000018010483,0.000097953525],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9995888,0.000087452805,0.00007099686,0.00010363235,0.000092074115,0.00005695951],"domain_scores_gemma":[0.9980501,0.0008710278,0.0006354833,0.00012303368,0.00012087881,0.00019955981],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00033576138,0.0006127143,0.00073807326,0.0013931938,0.00084246893,0.000652587,0.00050519046,0.0010409883,0.0035734808],"category_scores_gemma":[0.003683185,0.00042777864,0.00055425294,0.0012235105,0.00078497815,0.00040913664,0.0003059673,0.0005177095,0.00033726954],"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":[0.00041010737,0.000049930964,0.99359375,0.000019073046,0.000094784766,0.0025932677,0.00014137267,0.000060364466,0.0017058338,0.000051213363,0.00007239964,0.001207891],"study_design_scores_gemma":[0.00002292248,0.00014765967,0.9931079,0.000009455585,0.000114753704,0.0058392594,0.00015981568,0.00017916763,0.0001685045,0.00011964711,0.00012292997,0.0000080588115],"about_ca_topic_score_codex":0.0028705935,"about_ca_topic_score_gemma":0.0029630712,"teacher_disagreement_score":0.0035734808,"about_ca_system_score_codex":0.00022850798,"about_ca_system_score_gemma":0.00033914347,"threshold_uncertainty_score":0.011954486},"labels":[],"label_agreement":null},{"id":"W2586991018","doi":"10.4267/2042/61953","title":"A spontaneous dog model for a human sensory neuropathy: identification of a mutation in the upstream region of a neurotrophic factor","year":2016,"lang":"en","type":"article","venue":"Bulletin de l Académie vétérinaire de France","topic":"Hereditary Neurological Disorders","field":"Neuroscience","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 de Montréal","funders":"","keywords":"Glial cell line-derived neurotrophic factor; Neurotrophic factors; Genetics; Biology; Gene; Mutation; Coding region; Locus (genetics); Disease; Neuroscience; Bioinformatics; Medicine; Internal medicine","score_opus":0.036557336745768686,"score_gpt":0.27321649054899794,"score_spread":0.23665915380322924,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2586991018","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":[0.9969836,0.00024203431,0.0017684209,0.00010664607,0.00003518015,0.000051268402,0.00012607042,0.000031027103,0.0006558142],"genre_scores_gemma":[0.99517065,0.00029856808,0.0022519215,0.00008012817,0.000014957247,0.00008572019,0.00049729965,0.000012911709,0.0015877592],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.999819,0.000065624394,0.000013220742,0.00005509636,0.000023774879,0.000023422854],"domain_scores_gemma":[0.9998474,0.000047145102,0.000030270137,0.000026998616,0.000011106309,0.00003710257],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00029885606,0.0003444185,0.000258781,0.00034530836,0.00024150986,0.0001976055,0.0002187919,0.00041335533,0.0018663823],"category_scores_gemma":[0.00027024254,0.00013442193,0.00022765965,0.00012287888,0.00044265648,0.00027837153,0.00028378403,0.00042982286,0.00025594272],"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":[0.002532826,0.0024878443,0.02095489,0.00016093474,0.00007971946,0.009180452,0.0003433549,0.0003133389,0.9509787,0.0015483001,0.0008994042,0.010520278],"study_design_scores_gemma":[0.0018858891,0.050063565,0.16413833,0.0001364081,0.0006100563,0.17660175,0.0015334311,0.01346877,0.5560173,0.0026059765,0.032814223,0.00012435234],"about_ca_topic_score_codex":0.00030121827,"about_ca_topic_score_gemma":0.0007087664,"teacher_disagreement_score":0.0018663823,"about_ca_system_score_codex":0.0002163245,"about_ca_system_score_gemma":0.00023083485,"threshold_uncertainty_score":0.006243646},"labels":[],"label_agreement":null},{"id":"W2588646065","doi":"10.1097/cnd.0000000000000152","title":"Electrodiagnostic Characterization of Hereditary Neuropathy With Liability to Pressure Palsies","year":2017,"lang":"en","type":"article","venue":"Journal of Clinical Neuromuscular Disease","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":22,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":true,"ca_institutions":"London Health Sciences Centre; Western University","funders":"","keywords":"Medicine; Median nerve; Sural nerve; Ulnar nerve; Elbow; Nerve conduction study; Carpal tunnel syndrome; Polyneuropathy; Retrospective cohort study; Wrist; Nerve conduction; Surgery; Cohort; Anesthesia; Internal medicine","score_opus":0.05280056255772638,"score_gpt":0.347684533779468,"score_spread":0.29488397122174165,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2588646065","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":[0.9994254,0.00017599574,0.00007339085,0.000009819624,0.0000015713855,0.000004895012,0.00008462757,0.0000021483784,0.00022218177],"genre_scores_gemma":[0.9995908,0.0000810894,0.00006651156,0.000010076174,0.0000046327086,0.000003697789,0.00018305192,9.920528e-7,0.000059237565],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9995875,0.0000762062,0.00006522663,0.00011038137,0.00010024464,0.000060568796],"domain_scores_gemma":[0.9983222,0.00034823932,0.00083904347,0.00009085145,0.00023803183,0.00016170835],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0004990494,0.0002243524,0.00026102102,0.00090220297,0.00027245603,0.00037810244,0.0003079224,0.0002380959,0.0011535638],"category_scores_gemma":[0.0021388198,0.000109847024,0.00019843038,0.0005328991,0.00030854275,0.0003270217,0.00032837727,0.00014780069,0.00016885968],"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":[0.000044511115,0.000012077995,0.99648523,0.0000087824965,0.00001790939,0.0013678576,0.00003997339,0.000029191324,0.00085611554,0.000011191271,0.000032191096,0.001094944],"study_design_scores_gemma":[0.0000036743613,0.000082813,0.9888082,0.000007814074,0.000014042347,0.010561745,0.00012480836,0.00006859255,0.00021538457,0.000009525443,0.00010089454,0.0000024210703],"about_ca_topic_score_codex":0.0021008423,"about_ca_topic_score_gemma":0.0022042014,"teacher_disagreement_score":0.0021008423,"about_ca_system_score_codex":0.00022000163,"about_ca_system_score_gemma":0.00036657296,"threshold_uncertainty_score":0.0041772127},"labels":[],"label_agreement":null},{"id":"W2594817547","doi":"10.71781/30391","title":"Implication de la convertase NARC-1 / PCSK9 au cours de la différenciation neuroectodermale","year":2006,"lang":"fr","type":"dissertation","venue":"Papyrus : Institutional Repository (Université de Montréal)","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":0,"is_retracted":false,"has_abstract":false,"route_ca_aff":false,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"","funders":"Canadian Institutes of Health Research","keywords":"Chemistry","score_opus":0.005227906863829585,"score_gpt":0.19651926783424817,"score_spread":0.19129136097041857,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2594817547","genre_codex":"empirical","genre_gemma":"other","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"other","genre_consensus":null,"domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.96772367,0.011078151,0.0054159155,0.00083453173,0.00025962785,0.00008759177,0.00093057205,0.00020414116,0.0134656485],"genre_scores_gemma":[0.97911465,0.0024571451,0.002236133,0.00007641862,0.00004205757,0.000025638026,0.00064653426,0.00002185877,0.015379679],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9997347,0.000022157255,0.000019590127,0.000052735235,0.00009373946,0.00007708951],"domain_scores_gemma":[0.99970967,0.000076717224,0.00006051713,0.000030734936,0.000071107366,0.00005112799],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0003239225,0.0005160858,0.00034319283,0.00060776796,0.00057553744,0.0013012252,0.00042425262,0.0009416407,0.0031116267],"category_scores_gemma":[0.00050042744,0.00022738545,0.0005155774,0.00020563023,0.00048505157,0.00045078134,0.0002878483,0.0015235151,0.0009542284],"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":[0.00071080227,0.00007990275,0.0047655767,0.000114662325,0.000043960154,0.008699468,0.00013560931,0.00037900632,0.9666944,0.0028910157,0.0006447139,0.014840934],"study_design_scores_gemma":[0.000081691855,0.00020328052,0.050570577,0.00002531258,0.00006997725,0.007529784,0.00016781883,0.0009700367,0.9277946,0.0007696965,0.0117992675,0.000017989698],"about_ca_topic_score_codex":0.012788502,"about_ca_topic_score_gemma":0.007460855,"teacher_disagreement_score":0.012788502,"about_ca_system_score_codex":0.0013761183,"about_ca_system_score_gemma":0.000761484,"threshold_uncertainty_score":0.025428116},"labels":[{"model":"gemma","categories":[],"domain":null,"study_design":"bench_or_experimental","genre":"empirical","about_ca_system":false,"about_ca_topic":false,"confidence":"low"},{"model":"gpt","categories":[],"domain":null,"study_design":"bench_or_experimental","genre":"empirical","about_ca_system":false,"about_ca_topic":false,"confidence":"medium"}],"label_agreement":"agree"},{"id":"W2605720460","doi":"10.1111/cge.13037","title":"<i><scp>WNK1</scp>/<scp>HSN2</scp></i> founder mutation in patients with hereditary sensory and autonomic neuropathy: A Japanese cohort study","year":2017,"lang":"en","type":"article","venue":"Clinical Genetics","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":15,"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":"Japan Agency for Medical Research and Development","keywords":"Haplotype; Founder effect; Genetics; Cohort; Nonsense mutation; Mutation; Medicine; Genotype; Compound heterozygosity; Pathological; Biology; Gene; Internal medicine; Missense mutation","score_opus":0.052520130117094325,"score_gpt":0.31363719996879513,"score_spread":0.2611170698517008,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2605720460","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":[0.9993467,0.00016115588,0.000095563235,0.000016989836,0.000005772562,0.000013844831,0.00010385486,0.0000027622511,0.00025333295],"genre_scores_gemma":[0.9989231,0.00031839302,0.00014164613,0.000041240084,0.000017932329,0.000013053403,0.00031081907,0.000006292559,0.00022734284],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.999691,0.000037534697,0.000045984783,0.00012815832,0.0000498614,0.000047545553],"domain_scores_gemma":[0.99963653,0.000024462588,0.000074134216,0.000045841512,0.000071330156,0.00014766863],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0003539002,0.0005859053,0.00041130884,0.0008959967,0.0009080388,0.00046502904,0.00031541198,0.00034488822,0.0008970684],"category_scores_gemma":[0.00061861344,0.0004110658,0.0005036626,0.000740367,0.00034572932,0.0004055854,0.000647014,0.0003324946,0.00021691478],"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":[0.00012355405,0.00004215763,0.98938316,0.000023370834,0.000103853694,0.002965,0.00086680043,0.000041251486,0.0029798157,0.00002779151,0.00029206986,0.0031511916],"study_design_scores_gemma":[0.000022576969,0.00013359808,0.98805714,0.00001438667,0.00015547193,0.008932545,0.0007541175,0.00021981941,0.00029858228,0.00003060087,0.0013634361,0.000017659137],"about_ca_topic_score_codex":0.0124368975,"about_ca_topic_score_gemma":0.014089019,"teacher_disagreement_score":0.0124368975,"about_ca_system_score_codex":0.00028681196,"about_ca_system_score_gemma":0.00040006742,"threshold_uncertainty_score":0.024729013},"labels":[],"label_agreement":null},{"id":"W2606476851","doi":"10.1017/cjn.2015.158","title":"Auto-antibodies against gangliosides in patients with Charcot-Marie-Tooth disease","year":2015,"lang":"en","type":"article","venue":"Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":0,"is_retracted":false,"has_abstract":true,"route_ca_aff":false,"route_ca_fund":false,"route_ca_venue":true,"route_about_ca":false,"ca_institutions":"","funders":"","keywords":"Autoantibody; Bonferroni correction; Medicine; Antibody; Ganglioside; Antigen; Axon; Myelin; Autoimmunity; Myelin basic protein; Immunology; Statistical significance; Population; Internal medicine; Pathology; Biology; Genetics; Central nervous system; Anatomy","score_opus":0.04025647849665903,"score_gpt":0.2532509083894,"score_spread":0.21299442989274098,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2606476851","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":[0.9982204,0.0006916791,0.00004441415,0.00005979935,0.000007785673,0.0000078159055,0.00011021443,0.000012641142,0.00084534206],"genre_scores_gemma":[0.99948704,0.00018446651,0.00006094331,0.00003318354,0.000010845059,0.0000033468511,0.00008503748,0.0000018593456,0.00013328798],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99969697,0.00003256988,0.000028407736,0.00008413652,0.00008996915,0.000067996065],"domain_scores_gemma":[0.9993944,0.00015664457,0.00016073104,0.000022421904,0.000100457626,0.00016541478],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0003037656,0.0005391709,0.00043543524,0.0015798371,0.0010583245,0.00047832893,0.00031858915,0.00062208227,0.0026558242],"category_scores_gemma":[0.0011337072,0.00022212962,0.00020007431,0.0013067232,0.00045572929,0.00022160205,0.0002489449,0.000455564,0.00023183537],"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":[0.0005554037,0.00006571422,0.98278403,0.000062958716,0.00003690124,0.0067623025,0.0004597495,0.000058957274,0.004897258,0.000032141113,0.0003345532,0.003950099],"study_design_scores_gemma":[0.000013057879,0.000198276,0.9866468,0.000013106825,0.00004869692,0.01198674,0.00026334674,0.00009577436,0.00039068764,0.00003805672,0.0002988407,0.000006559505],"about_ca_topic_score_codex":0.026668292,"about_ca_topic_score_gemma":0.021195276,"teacher_disagreement_score":0.026668292,"about_ca_system_score_codex":0.000785858,"about_ca_system_score_gemma":0.0007190038,"threshold_uncertainty_score":0.05302608},"labels":[],"label_agreement":null},{"id":"W2607130795","doi":"10.1017/cjn.2015.90","title":"Hereditary neuropathy with liability to pressure palsies in childhood: case series and update from the literature","year":2015,"lang":"en","type":"article","venue":"Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques","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":true,"route_about_ca":false,"ca_institutions":"Systems, Applications & Products in Data Processing (Canada); Toronto Public Health","funders":"","keywords":"Mononeuropathy; Medicine; Palsy; Presentation (obstetrics); Carpal tunnel syndrome; Pediatrics; Carpal tunnel; Brachial plexus; Nerve conduction; Polyneuropathy; Surgery; Peripheral neuropathy; Pathology; Diabetes mellitus","score_opus":0.025955935064139544,"score_gpt":0.24095841426924888,"score_spread":0.21500247920510934,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2607130795","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":[0.70158535,0.2739706,0.0038820338,0.0027001912,0.0011699869,0.00041341633,0.0011181807,0.00036395853,0.014796246],"genre_scores_gemma":[0.87170565,0.1189086,0.0020728686,0.0014466374,0.0033779421,0.00008107973,0.0007392472,0.000041770036,0.001626123],"study_design_codex":"case_report","study_design_gemma":"case_report","domain_scores_codex":[0.99928814,0.00007432901,0.00022415491,0.00015040339,0.0001136626,0.00014931023],"domain_scores_gemma":[0.9983,0.00055508036,0.0006114785,0.00014141231,0.0001870367,0.00020496405],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00039719077,0.0015800769,0.0010976603,0.004638199,0.0009878888,0.0015174507,0.0011279071,0.0020873684,0.0029360265],"category_scores_gemma":[0.0018637564,0.0006549372,0.00068888604,0.0039120205,0.0013692525,0.0016084632,0.0012871092,0.00093513186,0.0010137564],"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":[0.000079464895,0.00012877384,0.058595896,0.0011494077,0.0001358694,0.90409523,0.0006135557,0.00023010754,0.001027884,0.00020477064,0.004244887,0.029494138],"study_design_scores_gemma":[0.000011257313,0.00004416854,0.019127045,0.00027628834,0.00010548539,0.9758607,0.00037374982,0.000092591785,0.0002126505,0.00015354475,0.0037201857,0.000022281107],"about_ca_topic_score_codex":0.00178314,"about_ca_topic_score_gemma":0.0026072839,"teacher_disagreement_score":0.004638199,"about_ca_system_score_codex":0.0006879462,"about_ca_system_score_gemma":0.00077572395,"threshold_uncertainty_score":0.009822011},"labels":[],"label_agreement":null},{"id":"W2613604943","doi":"10.11606/t.17.2017.tde-19072016-171042","title":"Avaliação clínica e neurofisiológica das possíveis consequências da intolerância à glicose ou do diabetes mellitus em pacientes com neuropatia sensitivo motora hereditária secundária à duplicação do cromossomo 17p11.2","year":2017,"lang":"pt","type":"dissertation","venue":"","topic":"Hereditary Neurological Disorders","field":"Neuroscience","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; Diabetes mellitus; Endocrinology","score_opus":0.0379136025811646,"score_gpt":0.30977454333477206,"score_spread":0.27186094075360745,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2613604943","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":[0.9915211,0.006260396,0.00019060863,0.00015357035,0.000019465899,0.00003338881,0.00033122164,0.000008055608,0.0014820872],"genre_scores_gemma":[0.9966114,0.0022149028,0.00024645298,0.00008960289,0.000040147406,0.000029054505,0.00029280275,0.0000023715734,0.00047320567],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99970895,0.000068223126,0.000044478133,0.00006909132,0.00004767872,0.0000616448],"domain_scores_gemma":[0.99883705,0.0003582537,0.00046023852,0.000043186308,0.00017532405,0.00012602156],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00075379194,0.00024125328,0.0004712137,0.0009127229,0.0003674268,0.0008700648,0.00019242997,0.00048050625,0.0021569068],"category_scores_gemma":[0.002410559,0.00015095642,0.0004934345,0.0010374053,0.00027389007,0.0005600007,0.00032234215,0.00042325043,0.00022585609],"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":[0.0012880488,0.00009193101,0.97665966,0.00019616832,0.00015449202,0.0012736771,0.00032113006,0.000063616295,0.0012198939,0.0000633809,0.00029028955,0.018377703],"study_design_scores_gemma":[0.000042535947,0.00089061103,0.9921118,0.000088202454,0.00019939155,0.003989583,0.000745484,0.00023790261,0.00032093388,0.00013843771,0.0012182002,0.000017035152],"about_ca_topic_score_codex":0.003130406,"about_ca_topic_score_gemma":0.0035823784,"teacher_disagreement_score":0.003130406,"about_ca_system_score_codex":0.000381461,"about_ca_system_score_gemma":0.00040441594,"threshold_uncertainty_score":0.007215619},"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":"W2619491058","doi":"10.1016/j.celrep.2017.05.018","title":"Effect of Human Genetic Variability on Gene Expression in Dorsal Root Ganglia and Association with Pain Phenotypes","year":2017,"lang":"en","type":"article","venue":"Cell Reports","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":69,"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; McGill University","funders":"National Institute of Dental and Craniofacial Research; National Institutes of Health; University of North Carolina Wilmington; McGill University; University of Pittsburgh; National Institute on Aging; Duke University","keywords":"Phenotype; Gene; Dorsum; Biology; Genetics; Gene expression; Association (psychology); Neuroscience; Anatomy; Psychology","score_opus":0.010412696946599234,"score_gpt":0.24644841883811483,"score_spread":0.2360357218915156,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2619491058","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":[0.9978483,0.00024468004,0.0006447825,0.000037920883,0.0000043551177,0.0000032763826,0.0007860526,0.000010495049,0.00041997232],"genre_scores_gemma":[0.998865,0.00010131095,0.00035993458,0.000021697768,0.00000426041,0.000003905008,0.0004884646,0.000009263083,0.00014611722],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9992506,0.00023407249,0.00007118087,0.0003097915,0.00008226244,0.00005197988],"domain_scores_gemma":[0.9991812,0.00044525063,0.00015024681,0.00013237906,0.000031544303,0.000059378755],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00041679674,0.00019482261,0.00023190698,0.000859762,0.00020253166,0.0003925414,0.00017142209,0.00031138703,0.002564903],"category_scores_gemma":[0.0012790771,0.00010182452,0.00030909563,0.0007934145,0.00035218874,0.00010254519,0.0003336765,0.00025078192,0.0001807549],"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":[0.0011269443,0.000061023326,0.90932393,0.000069835995,0.00096623943,0.0012797822,0.00030495747,0.00086793146,0.07195335,0.0005644082,0.00035622861,0.013125431],"study_design_scores_gemma":[0.000016134223,0.000061181374,0.9957482,0.0000073871174,0.00011947495,0.0009899788,0.00006363465,0.0006224336,0.0016829615,0.00037154878,0.000310183,0.0000069241123],"about_ca_topic_score_codex":0.0016592164,"about_ca_topic_score_gemma":0.0019037421,"teacher_disagreement_score":0.002564903,"about_ca_system_score_codex":0.00010315424,"about_ca_system_score_gemma":0.000072157665,"threshold_uncertainty_score":0.008580446},"labels":[],"label_agreement":null},{"id":"W2620788257","doi":"10.1017/cjn.2017.204","title":"Effects of Self-Selected Exercise on Strength in Charcot–Marie–Tooth Disease Subtypes","year":2017,"lang":"en","type":"article","venue":"Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":8,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":true,"route_about_ca":false,"ca_institutions":"McMaster University Medical Centre; University of Guelph; McMaster University","funders":"","keywords":"Medicine; Physical therapy; Grip strength; Elbow flexion; Pes cavus; Elbow; Tooth disease; Population; Physical medicine and rehabilitation; Disease; Internal medicine; Surgery","score_opus":0.023470606540178254,"score_gpt":0.25764716995858994,"score_spread":0.2341765634184117,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2620788257","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":[0.99944085,0.00023883572,0.000009309448,0.00001476153,0.0000018121035,0.0000056014933,0.000055896115,8.5430855e-7,0.0002320454],"genre_scores_gemma":[0.9996562,0.000088097506,0.00003604422,0.000010193874,0.0000032609962,0.0000068535296,0.00009852603,7.4804603e-7,0.00010004944],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99960023,0.00014565249,0.000040933228,0.00007221386,0.0000916155,0.000049313723],"domain_scores_gemma":[0.9975999,0.00070911803,0.0010982346,0.00008149536,0.00017336584,0.0003378965],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00090818637,0.0001667297,0.0003000328,0.00050836627,0.00023681311,0.00031162522,0.00026106212,0.00027118513,0.0010968068],"category_scores_gemma":[0.003939475,0.000087231565,0.00038360764,0.00039587033,0.00019177493,0.00015467101,0.0002219994,0.0002049244,0.00010050926],"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":[0.0005813139,0.0001332081,0.99442565,0.000020111052,0.00009822347,0.00006689061,0.000052117808,0.000050137027,0.00017882988,0.0000054717134,0.000042112162,0.0043459353],"study_design_scores_gemma":[0.000008725773,0.00018850302,0.99956864,0.0000047285416,0.000016136279,0.00008717593,0.00003184203,0.000039735332,0.000025547193,0.0000049012824,0.000023183073,9.071183e-7],"about_ca_topic_score_codex":0.0051187994,"about_ca_topic_score_gemma":0.01229024,"teacher_disagreement_score":0.0051187994,"about_ca_system_score_codex":0.00039309694,"about_ca_system_score_gemma":0.00018175988,"threshold_uncertainty_score":0.01017797},"labels":[],"label_agreement":null},{"id":"W2621608471","doi":"10.1007/s12035-017-0574-7","title":"A BRCA1-Dependent DNA Damage Response in the Regenerating Adult Peripheral Nerve Milieu","year":2017,"lang":"en","type":"article","venue":"Molecular Neurobiology","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":21,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Ontario Brain Institute; Hotchkiss Brain Institute; Women and Children’s Health Research Institute; University of Calgary; University of Alberta","funders":"Canadian Institutes of Health Research; Alberta Innovates - Health Solutions; University of Alberta; Canadian Diabetes Association","keywords":"DNA damage; Regeneration (biology); Biology; Neuroscience; DNA repair; Cell biology; Phenotype; Schwann cell; DNA; Genetics; Gene","score_opus":0.02519965645582105,"score_gpt":0.2753056341956304,"score_spread":0.25010597773980936,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2621608471","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":[0.98225015,0.0075379014,0.004504773,0.0005541756,0.00007482319,0.000046001933,0.00054765027,0.00018084579,0.0043036924],"genre_scores_gemma":[0.9892096,0.0017756331,0.0020308297,0.00016798575,0.00002197567,0.000029274568,0.0005247348,0.00002037941,0.0062197484],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99987376,0.000016131522,0.0000061361166,0.000036505953,0.000033877823,0.000033619635],"domain_scores_gemma":[0.9998536,0.00001706004,0.00002915122,0.000017120292,0.000027500715,0.00005540081],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00018687572,0.00023326415,0.00026138464,0.00026352986,0.000278185,0.00043331704,0.0002586426,0.00037820678,0.0025000302],"category_scores_gemma":[0.00020495745,0.00012771788,0.0001856179,0.00008583065,0.00034526605,0.000404721,0.0003408637,0.00054362067,0.00060871406],"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":[0.00014374129,0.000013446464,0.00051381055,0.000056460758,0.000005833337,0.00023487298,0.000046542184,0.00007829946,0.9962065,0.00034545248,0.00017797701,0.0021771248],"study_design_scores_gemma":[0.000033747205,0.00045530839,0.059351496,0.00005653339,0.000024251327,0.0033448837,0.00026623736,0.0010016446,0.9289227,0.0008352453,0.005690419,0.000017518958],"about_ca_topic_score_codex":0.0005825384,"about_ca_topic_score_gemma":0.00072224735,"teacher_disagreement_score":0.0025000302,"about_ca_system_score_codex":0.0004257703,"about_ca_system_score_gemma":0.00030415595,"threshold_uncertainty_score":0.008363426},"labels":[],"label_agreement":null},{"id":"W2730213721","doi":"10.1002/mus.22199","title":"Sonographic features in hereditary neuropathy with liability to pressure palsies","year":2011,"lang":"en","type":"article","venue":"Muscle & Nerve","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":50,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"McMaster University; Hamilton Health Sciences; Hamilton General Hospital; University of Manitoba; Riverview Hospital","funders":"","keywords":"Medicine; Ankle; Tibial nerve; Elbow; Wrist; Ulnar nerve; Ulnar neuropathy; Median nerve; Ultrasound; Anatomy; Surgery; Physical medicine and rehabilitation; Radiology; Internal medicine; Stimulation","score_opus":0.035236188392893886,"score_gpt":0.22861045869469662,"score_spread":0.19337427030180274,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2730213721","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":[0.9996263,0.00008045108,0.00006253054,0.000009439386,0.0000012364907,0.00000255852,0.000017887865,0.000003486706,0.00019616743],"genre_scores_gemma":[0.9996848,0.000054298544,0.00012784649,0.0000057895913,0.000006107183,0.0000026418352,0.000036470592,0.0000010163117,0.00008109138],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.999808,0.000047086993,0.000025377798,0.000045982186,0.000044610664,0.000028919432],"domain_scores_gemma":[0.99916947,0.00025306467,0.00033392178,0.00002848686,0.00007379296,0.00014131455],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00041586827,0.00044406365,0.0002614674,0.0014448452,0.00024495597,0.0002279894,0.0001901109,0.00028067594,0.0034043042],"category_scores_gemma":[0.0018850367,0.00016837864,0.00008623173,0.00044651263,0.00054504076,0.0002620014,0.00034403897,0.0001701738,0.00018370153],"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":[0.00034651294,0.00008311735,0.9772012,0.000045912137,0.00003547169,0.007673146,0.0004165911,0.00008868916,0.008424739,0.000044045482,0.000088283596,0.005552194],"study_design_scores_gemma":[0.000011117974,0.0004319092,0.97635514,0.0000112966545,0.0000287248,0.021731904,0.00028467865,0.00014129879,0.0008540852,0.000040670377,0.000105442065,0.0000037313923],"about_ca_topic_score_codex":0.0011654467,"about_ca_topic_score_gemma":0.0010743128,"teacher_disagreement_score":0.0034043042,"about_ca_system_score_codex":0.00014608096,"about_ca_system_score_gemma":0.0001511742,"threshold_uncertainty_score":0.011388481},"labels":[],"label_agreement":null},{"id":"W2731978562","doi":"10.1016/j.jns.2017.07.011","title":"Spastic paraplegia type 4: A novel SPAST splice site donor mutation and expansion of the phenotype variability","year":2017,"lang":"en","type":"article","venue":"Journal of the Neurological Sciences","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":19,"is_retracted":false,"has_abstract":false,"route_ca_aff":false,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"","funders":"Japan Society for the Promotion of Science; University of Tokushima; Ministero della Salute; Canada Excellence Research Chairs, Government of Canada; Japan Agency for Medical Research and Development","keywords":"Hereditary spastic paraplegia; splice; Phenotype; Paraplegia; Mutation; Spastic; Splice site mutation; Genetics; Medicine; Biology; RNA splicing; Physical medicine and rehabilitation; Neuroscience; Gene; Spinal cord; Cerebral palsy","score_opus":0.05636063108138603,"score_gpt":0.29014694638761457,"score_spread":0.23378631530622854,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2731978562","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":[0.9914022,0.00026014983,0.0031199702,0.0006523826,0.00022027142,0.00012780871,0.00085006066,0.0001510909,0.0032160522],"genre_scores_gemma":[0.996363,0.000079352096,0.0015536223,0.00019743058,0.00013860964,0.000033904515,0.0003227169,0.000041520005,0.0012699906],"study_design_codex":"case_report","study_design_gemma":"observational","domain_scores_codex":[0.9995128,0.00008962581,0.00009821677,0.00011524656,0.00009841123,0.00008573125],"domain_scores_gemma":[0.9991436,0.00034616963,0.0002002842,0.000058450234,0.00007311995,0.00017825881],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0002413041,0.001996823,0.00094467844,0.0013311356,0.00096044486,0.00038958993,0.0010022761,0.0022502418,0.0059681595],"category_scores_gemma":[0.0016472711,0.00031858613,0.001308301,0.0007030911,0.0009321345,0.00031296653,0.000836716,0.0012132342,0.0009579002],"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":[0.0010324747,0.000383887,0.018111909,0.00016302381,0.00018782311,0.80174875,0.00047255598,0.0010935026,0.16260758,0.001622542,0.0011185592,0.011457443],"study_design_scores_gemma":[0.0004884921,0.0013282923,0.08589352,0.00010044186,0.0004510396,0.8386241,0.00036752812,0.0062513785,0.05844395,0.0025492634,0.005323356,0.00017867147],"about_ca_topic_score_codex":0.0020669547,"about_ca_topic_score_gemma":0.0018717659,"teacher_disagreement_score":0.0059681595,"about_ca_system_score_codex":0.000501036,"about_ca_system_score_gemma":0.0006731456,"threshold_uncertainty_score":0.01996547},"labels":[],"label_agreement":null},{"id":"W2735161849","doi":"10.1111/cge.13101","title":"Whole‐exome sequencing is a valuable diagnostic tool for inherited peripheral neuropathies: Outcomes from a cohort of 50 families","year":2017,"lang":"en","type":"article","venue":"Clinical Genetics","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":59,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"BC Children's Hospital; SickKids Foundation; University of Toronto; Alberta Children's Hospital; Children's Hospital of Eastern Ontario; McGill University; University of Calgary; University of British Columbia; Hospital for Sick Children; McMaster University Medical Centre; University of Ottawa","funders":"Canadian Institutes of Health Research; Ontario Genomics Institute","keywords":"Exome sequencing; Exome; Cohort; Medicine; Genetics; Bioinformatics; Biology; Mutation; Pathology; Gene","score_opus":0.164135244841846,"score_gpt":0.37969317386706775,"score_spread":0.21555792902522175,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2735161849","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":[0.9994405,0.00007199131,0.0001096463,0.00001373796,0.0000015618741,0.0000071438863,0.00013705213,0.0000051112197,0.00021327553],"genre_scores_gemma":[0.9989773,0.0001423412,0.00015377667,0.000030314197,0.0000052231453,0.000010453153,0.00045466115,0.000006112372,0.00021987088],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99953103,0.00011103563,0.000037894013,0.00015699204,0.0000950899,0.0000679503],"domain_scores_gemma":[0.99932885,0.0001740347,0.00015118525,0.00011608423,0.0000984179,0.00013150717],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0007235393,0.0005359238,0.0003259326,0.00071619893,0.00075917924,0.0007734992,0.00024223723,0.00043028238,0.00083387963],"category_scores_gemma":[0.0023074073,0.0002304865,0.00037093184,0.00048788314,0.0004877699,0.00041938195,0.0010182458,0.00030364312,0.00032623482],"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":[0.00029146095,0.00014777722,0.9783589,0.000015365777,0.00011649352,0.0050767213,0.0014150556,0.00025330632,0.004760076,0.000050321072,0.00036626696,0.00914823],"study_design_scores_gemma":[0.000020726222,0.000359489,0.9899828,0.000015792222,0.00008451304,0.007276553,0.0005596254,0.00036533226,0.0006581986,0.000058029644,0.00060199003,0.000016974183],"about_ca_topic_score_codex":0.0060535152,"about_ca_topic_score_gemma":0.005009174,"teacher_disagreement_score":0.0060535152,"about_ca_system_score_codex":0.00028130657,"about_ca_system_score_gemma":0.00023923663,"threshold_uncertainty_score":0.012036562},"labels":[],"label_agreement":null},{"id":"W2740480502","doi":"10.1016/j.ejmg.2017.07.015","title":"A de novo mosaic mutation in SPAST with two novel alternative alleles and chromosomal copy number variant in a boy with spastic paraplegia and autism spectrum disorder","year":2017,"lang":"en","type":"article","venue":"European Journal of Medical Genetics","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":15,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Vancouver Native Health Society; BC Children's Hospital; Pacific Centre for Reproductive Medicine; University of British Columbia","funders":"Canadian Institutes of Health Research; Genome British Columbia","keywords":"Genetics; Hereditary spastic paraplegia; Missense mutation; Biology; Allele; Exome sequencing; Heritability of autism; Copy-number variation; Phenotype; Gene duplication; Autism; Spastic; Medicine; Gene; Genome","score_opus":0.021427688787372803,"score_gpt":0.2743353690526588,"score_spread":0.25290768026528604,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2740480502","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":[0.995432,0.00034283314,0.0011429435,0.0006876626,0.00008391582,0.000036961632,0.0003641916,0.00008325389,0.0018262478],"genre_scores_gemma":[0.99775416,0.00012338313,0.0011279831,0.00009541231,0.00008850636,0.000013267162,0.000076993165,0.000026553122,0.0006937866],"study_design_codex":"case_report","study_design_gemma":"case_report","domain_scores_codex":[0.9993345,0.000061885665,0.00007622994,0.0002331068,0.00015098134,0.00014332151],"domain_scores_gemma":[0.9983859,0.00059903256,0.00039048403,0.00005475964,0.000080888145,0.00048893155],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00026125758,0.0021879892,0.001005963,0.0018563167,0.0015163234,0.00070442946,0.0013911063,0.002897562,0.004491914],"category_scores_gemma":[0.0018929915,0.00079555134,0.0010951787,0.0009913146,0.0019315226,0.00068897003,0.0013857326,0.0015103437,0.0007028664],"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":[0.00007835003,0.00002930548,0.004462467,0.000025733669,0.000015464715,0.98699385,0.00021563577,0.00016130593,0.0068783876,0.00025767667,0.00012865901,0.0007531831],"study_design_scores_gemma":[0.00003895758,0.00016777824,0.020014854,0.000021408807,0.000059152444,0.97512054,0.0002461136,0.00071634864,0.002814123,0.00022179722,0.00055190903,0.000027027905],"about_ca_topic_score_codex":0.0030489957,"about_ca_topic_score_gemma":0.0032132906,"teacher_disagreement_score":0.004491914,"about_ca_system_score_codex":0.0006346705,"about_ca_system_score_gemma":0.0009743451,"threshold_uncertainty_score":0.015026987},"labels":[],"label_agreement":null},{"id":"W2743303297","doi":"10.1002/ana.25009","title":"Natural history of Charcot‐Marie‐Tooth disease during childhood","year":2017,"lang":"en","type":"article","venue":"Annals of Neurology","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":77,"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; Natural Sciences and Engineering Research Council of Canada; Medical Research Council; National Institute for Health and Care Research","keywords":"Confidence interval; Internal medicine; Natural history study; Medicine; Natural history; Balance (ability); Anthropometry; Demography; Physical therapy","score_opus":0.07443960457479172,"score_gpt":0.29611729767085576,"score_spread":0.22167769309606405,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2743303297","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":[0.9991049,0.0002626698,0.0000612637,0.0000304726,0.0000026284747,0.000005105164,0.00035144764,0.000006228917,0.00017533563],"genre_scores_gemma":[0.9991492,0.00013906858,0.000081892395,0.000015444448,0.000005467348,0.000008584889,0.0004785206,0.0000031279542,0.000118683114],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9992924,0.00018154686,0.00005412681,0.0002102256,0.00014506762,0.00011668478],"domain_scores_gemma":[0.99656725,0.00041868901,0.0020781248,0.00014348744,0.00033168474,0.00046064996],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.001136051,0.00031514143,0.0003214531,0.00092003524,0.0006082443,0.00074766844,0.00046732204,0.00071073306,0.00071668916],"category_scores_gemma":[0.003332476,0.00034224123,0.00047736263,0.0006897115,0.00039424642,0.00072949077,0.000499762,0.00071174226,0.00017668582],"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":[0.00007564552,0.000014223176,0.99903166,0.0000029438029,0.000018624882,0.00010203331,0.00006868548,0.00002429462,0.00014709661,0.0000045117454,0.000030145029,0.00048003817],"study_design_scores_gemma":[0.000002080013,0.00007097761,0.99908614,0.0000040760037,0.000009105551,0.00061092793,0.000072762516,0.000046797108,0.000040769464,0.000005214969,0.00004900494,0.0000021651601],"about_ca_topic_score_codex":0.010500802,"about_ca_topic_score_gemma":0.008341602,"teacher_disagreement_score":0.010500802,"about_ca_system_score_codex":0.000491359,"about_ca_system_score_gemma":0.0003710121,"threshold_uncertainty_score":0.020879328},"labels":[],"label_agreement":null},{"id":"W2744401277","doi":"10.1002/mus.26500","title":"Balance impairment in pediatric charcot–marie–tooth disease","year":2019,"lang":"en","type":"article","venue":"Muscle & Nerve","topic":"Hereditary Neurological Disorders","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 Institute of Neurological Disorders and Stroke; Medical Research Council; University of Sydney; University College London; National Institute for Health and Care Research; National Health and Medical Research Council; Natural Sciences and Engineering Research Council of Canada; Muscular Dystrophy Association; Charcot-Marie-Tooth Association","keywords":"Tooth disease; Balance (ability); Medicine; Physical medicine and rehabilitation; Disease; Internal medicine","score_opus":0.017380906089611126,"score_gpt":0.23425241966784058,"score_spread":0.21687151357822945,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2744401277","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":[0.99877006,0.00056500855,0.000055770935,0.00004509758,0.000004232606,0.00000519145,0.00015425438,0.000005120111,0.0003952167],"genre_scores_gemma":[0.9993697,0.00029793466,0.00008543822,0.00001606234,0.0000064725646,0.0000057493944,0.00014397262,0.0000011604114,0.0000735162],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9996369,0.000072985036,0.0000411431,0.00008923512,0.0001029419,0.0000568006],"domain_scores_gemma":[0.9990012,0.00015801389,0.0006079486,0.000017508575,0.000098530974,0.0001167848],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00048569098,0.0005166014,0.00048274983,0.0010423944,0.0003697833,0.0004267486,0.0001995329,0.00041349858,0.0015167146],"category_scores_gemma":[0.0017633185,0.00019492331,0.00022658489,0.0009226077,0.00033707923,0.00036430208,0.0003658229,0.00032481775,0.00016276154],"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":[0.0000735896,0.000026902213,0.99546534,0.000028375462,0.00002147267,0.0010331707,0.000075402444,0.000054426746,0.00037169925,0.0000113810165,0.00012525561,0.0027129946],"study_design_scores_gemma":[0.0000031990605,0.00007825033,0.995926,0.000015211674,0.000012695497,0.0036585901,0.000068083486,0.00007923858,0.00006883757,0.000012996638,0.000075262506,0.0000016668806],"about_ca_topic_score_codex":0.006919981,"about_ca_topic_score_gemma":0.0071671912,"teacher_disagreement_score":0.006919981,"about_ca_system_score_codex":0.00046418468,"about_ca_system_score_gemma":0.00039184693,"threshold_uncertainty_score":0.013759375},"labels":[],"label_agreement":null},{"id":"W2747467654","doi":"10.1017/cjn.2016.435","title":"Traduction française de l’échelle Charcot-Marie-Tooth Disease Pediatric Scale","year":2017,"lang":"fr","type":"article","venue":"Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":8,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":true,"route_about_ca":false,"ca_institutions":"Centre Hospitalier Universitaire Sainte-Justine; McGill University; Centre Intégré Universitaire de Santé et de Services Sociaux du Saguenay–Lac-Saint-Jean; Montreal Neurological Institute and Hospital; Université de Sherbrooke","funders":"","keywords":"Humanities; Medicine; Philosophy","score_opus":0.03992887065725558,"score_gpt":0.26986589488585416,"score_spread":0.22993702422859857,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2747467654","genre_codex":"empirical","genre_gemma":"other","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"other","genre_consensus":null,"domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.68907535,0.017554887,0.046656165,0.015757851,0.005423942,0.009140895,0.052710917,0.0017808335,0.16189913],"genre_scores_gemma":[0.81614256,0.0063147726,0.10513033,0.0024572483,0.0005479778,0.011456374,0.02232226,0.00041098375,0.035217464],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.98564917,0.0049677975,0.002703438,0.00078795425,0.0053315526,0.0005601833],"domain_scores_gemma":[0.9639692,0.01172056,0.005819021,0.0018573592,0.0155303,0.0011035892],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.016214801,0.00072976924,0.0006796638,0.0030707566,0.0009184141,0.0016346438,0.00088834524,0.00059288566,0.00633401],"category_scores_gemma":[0.029733945,0.00023977601,0.0011045245,0.0019689596,0.0011123159,0.0008231202,0.0015421808,0.0013627075,0.0018609813],"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":[0.0013873867,0.0004753207,0.35657334,0.0015448647,0.00047804712,0.00064050657,0.004841488,0.0009171321,0.0054324055,0.008070263,0.09117611,0.5284632],"study_design_scores_gemma":[0.00022928801,0.0007785116,0.7345658,0.0011724916,0.00015549583,0.0010985628,0.0025934542,0.0007222457,0.0028285938,0.0017098272,0.25397694,0.00016882923],"about_ca_topic_score_codex":0.022570517,"about_ca_topic_score_gemma":0.036657196,"teacher_disagreement_score":0.022570517,"about_ca_system_score_codex":0.0031331657,"about_ca_system_score_gemma":0.004570082,"threshold_uncertainty_score":0.08575308},"labels":[],"label_agreement":null},{"id":"W2754707874","doi":"10.1111/apa.14058","title":"Response Letter to ‘Optimising physiology for adolescents with dysautonomia’","year":2017,"lang":"en","type":"letter","venue":"Acta Paediatrica","topic":"Hereditary Neurological Disorders","field":"Neuroscience","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":"Simon Fraser University; University of British Columbia; BC Children's Hospital","funders":"","keywords":"Medicine; Pediatrics; Library science; Gerontology; Family medicine","score_opus":0.034489472229615334,"score_gpt":0.2662606958418341,"score_spread":0.23177122361221875,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2754707874","genre_codex":"commentary","genre_gemma":"commentary","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"commentary","genre_consensus":"commentary","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.000694714,0.0009315808,0.00008330508,0.95670027,0.038796745,0.000016500786,0.0000639381,0.000046834044,0.0026661528],"genre_scores_gemma":[0.007764528,0.0014870684,0.0002456429,0.8968146,0.081707865,0.00007077599,0.00007019421,0.000050585953,0.011788734],"study_design_codex":"not_applicable","study_design_gemma":"not_applicable","domain_scores_codex":[0.9982893,0.00037632376,0.0002823097,0.00022602596,0.00037749702,0.0004485659],"domain_scores_gemma":[0.99419206,0.0029020275,0.0006022555,0.00013983832,0.0011269962,0.0010368163],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0014415805,0.00088963954,0.001415405,0.00073431875,0.0029049818,0.0027036786,0.0013440107,0.045007557,0.0113604665],"category_scores_gemma":[0.023789937,0.0005930614,0.0013159147,0.0004910172,0.0019267383,0.002026985,0.0016395007,0.025992071,0.008303853],"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":[0.00005251733,0.000032008367,0.0009406245,0.00006547004,0.000016728367,0.008068824,0.00013578743,0.000085428204,0.00011808312,0.0009193582,0.9831782,0.0063869352],"study_design_scores_gemma":[0.00028202115,0.00018980939,0.003617808,0.0011000285,0.0000706168,0.020966126,0.0011398213,0.0009978791,0.00035390214,0.007689789,0.96345896,0.00013326413],"about_ca_topic_score_codex":0.0044479277,"about_ca_topic_score_gemma":0.0071527073,"teacher_disagreement_score":0.045007557,"about_ca_system_score_codex":0.0035844657,"about_ca_system_score_gemma":0.0032450273,"threshold_uncertainty_score":0.038004518},"labels":[],"label_agreement":null},{"id":"W2765097431","doi":"10.71781/27177","title":"Altérations des cellules de Schwann périsynaptiques à la jonction neuromusculaire : implications pour la sclérose latérale amyotrophique","year":2016,"lang":"fr","type":"dissertation","venue":"Papyrus : Institutional Repository (Université de Montréal)","topic":"Hereditary Neurological Disorders","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":"Robert Packard Center for ALS Research, Johns Hopkins University; Canadian Institutes of Health Research; Muscular Dystrophy Association; Johns Hopkins University; Fondation Brain Canada; ALS Society of Canada","keywords":"Medicine; Humanities; Art","score_opus":0.011944900528689307,"score_gpt":0.20262780690037044,"score_spread":0.19068290637168114,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2765097431","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":[0.8458867,0.12349212,0.0109426975,0.003966094,0.00055514625,0.0000755018,0.00038323348,0.00017214006,0.014526396],"genre_scores_gemma":[0.9485556,0.035293207,0.0045161108,0.00076440774,0.00012300577,0.000092482886,0.00018845935,0.000027240554,0.010439491],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9997211,0.000051446255,0.000017984914,0.000056135388,0.0000912155,0.000062152925],"domain_scores_gemma":[0.9996051,0.000064309745,0.00012253749,0.000026452864,0.00010460456,0.000077039695],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0006357627,0.00045131968,0.00040068288,0.00089930504,0.0008531379,0.0012434372,0.0003933976,0.0012919522,0.0030783885],"category_scores_gemma":[0.0005991488,0.00023001428,0.0006162293,0.0006142269,0.0014004655,0.0012826317,0.00057349337,0.0009840769,0.00088971923],"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":[0.000835739,0.00012733371,0.022862589,0.0014690663,0.00015814583,0.007920311,0.0013211532,0.00059719884,0.9000531,0.006292242,0.0008536468,0.05750947],"study_design_scores_gemma":[0.00018414404,0.0026359286,0.43538997,0.0016614378,0.00063348643,0.045638688,0.012904269,0.0037174376,0.38007972,0.013307045,0.103609696,0.0002381399],"about_ca_topic_score_codex":0.0035489951,"about_ca_topic_score_gemma":0.004349651,"teacher_disagreement_score":0.0035489951,"about_ca_system_score_codex":0.0010553845,"about_ca_system_score_gemma":0.0008224024,"threshold_uncertainty_score":0.010298252},"labels":[],"label_agreement":null},{"id":"W2765118358","doi":"10.1136/jmedgenet-2017-104748","title":"Expanding the clinical spectrum of recessive truncating mutations of <i>KLHL7</i> to a Bohring-Opitz-like phenotype","year":2017,"lang":"en","type":"article","venue":"Journal of Medical Genetics","topic":"Hereditary Neurological Disorders","field":"Neuroscience","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":"McGill University Health Centre","funders":"Conseil régional de Bourgogne-Franche-Comté","keywords":"Genetics; Microcephaly; Exome sequencing; Phenotype; Biology; Genetic heterogeneity; Compound heterozygosity; Medical genetics; Mutation; Gene","score_opus":0.10720118682676634,"score_gpt":0.4100622003835627,"score_spread":0.3028610135567964,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2765118358","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":[0.9943963,0.00058854616,0.0013132722,0.00015601405,0.000018098766,0.00004186378,0.00022614001,0.00009637467,0.0031634453],"genre_scores_gemma":[0.9979001,0.00027310313,0.0011576063,0.00015435243,0.000038608978,0.000012299918,0.00015870886,0.000022717599,0.00028235256],"study_design_codex":"case_report","study_design_gemma":"observational","domain_scores_codex":[0.99958783,0.00005159145,0.00007077708,0.000110637615,0.00008716346,0.000092058755],"domain_scores_gemma":[0.9994529,0.00017344802,0.00013421109,0.000028143417,0.000060651906,0.00015076052],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00032071842,0.0014280288,0.0005203283,0.0012144847,0.00050148414,0.00038449545,0.0003796217,0.00056755147,0.002379363],"category_scores_gemma":[0.0008368882,0.0002114962,0.0004952595,0.0006128273,0.00077446096,0.00025029937,0.0009771264,0.00047690666,0.00031254074],"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":[0.00067843474,0.00016647176,0.24021362,0.0003534055,0.00015081669,0.49342337,0.0014643734,0.0010113267,0.21819434,0.0011071748,0.002082012,0.041154604],"study_design_scores_gemma":[0.00011865439,0.00037420404,0.2168871,0.00007765414,0.00014496181,0.75925064,0.00040229515,0.0010580358,0.017870372,0.00048755354,0.003289159,0.000039324575],"about_ca_topic_score_codex":0.0008252489,"about_ca_topic_score_gemma":0.0011224797,"teacher_disagreement_score":0.002379363,"about_ca_system_score_codex":0.0002403551,"about_ca_system_score_gemma":0.00032625534,"threshold_uncertainty_score":0.0079597235},"labels":[],"label_agreement":null},{"id":"W2765213916","doi":"10.1007/978-3-319-61361-1_18","title":"Acquired and Hereditary Neuropathies","year":2017,"lang":"en","type":"book-chapter","venue":"","topic":"Hereditary Neurological Disorders","field":"Neuroscience","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":"University of Ottawa; Children's Hospital of Eastern Ontario","funders":"","keywords":"Medicine","score_opus":0.05699433203593976,"score_gpt":0.2532888804676819,"score_spread":0.19629454843174213,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2765213916","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":[0.0019878661,0.12272298,0.0025100317,0.0033296433,0.0036630963,0.000022334285,0.00019075137,0.00014683272,0.8654264],"genre_scores_gemma":[0.012693786,0.09087283,0.0021728026,0.0025196166,0.0026003132,0.00004267784,0.00036846765,0.00010222019,0.8886273],"study_design_codex":"not_applicable","study_design_gemma":"not_applicable","domain_scores_codex":[0.9998969,0.000015431939,0.000005159045,0.000014295421,0.0000499838,0.000018288134],"domain_scores_gemma":[0.9999354,0.00002705912,0.0000049267983,0.0000057682123,0.000014628057,0.000012246141],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00013911631,0.0006783437,0.00032199692,0.0008274379,0.00042207693,0.0009186298,0.0005354686,0.0007809894,0.036249932],"category_scores_gemma":[0.0003416165,0.00016215448,0.000190561,0.0006162106,0.00077522,0.0012065282,0.0011780693,0.0014371291,0.009277966],"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":[0.000027137601,0.00005025012,0.00021229214,0.00040619928,0.000010623499,0.0012540699,0.0003825297,0.0005142414,0.0008543136,0.14454111,0.54688305,0.30486417],"study_design_scores_gemma":[0.0000021763099,0.000006214897,0.00019348253,0.00021349045,0.000002785944,0.0017445342,0.000042943888,0.00005266324,0.00009541885,0.014803242,0.98284,0.0000030323265],"about_ca_topic_score_codex":0.0012913892,"about_ca_topic_score_gemma":0.005072208,"teacher_disagreement_score":0.036249932,"about_ca_system_score_codex":0.0006642466,"about_ca_system_score_gemma":0.0007637445,"threshold_uncertainty_score":0.12126809},"labels":[],"label_agreement":null},{"id":"W2765642329","doi":"10.1007/978-3-319-61361-1_2","title":"Anatomy and Physiology of Peripheral Nerves","year":2017,"lang":"en","type":"book-chapter","venue":"","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":1,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Ottawa; Children's Hospital of Eastern Ontario","funders":"","keywords":"Peripheral; Anatomy; Gross anatomy; Electromyography; Peripheral nervous system; Cranial nerves; Neuroscience; Nerve conduction; Medicine; Biology; Central nervous system; Surgery; Internal medicine","score_opus":0.043258188156007134,"score_gpt":0.2774759916082613,"score_spread":0.23421780345225418,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2765642329","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":[0.0011929296,0.17131537,0.013540203,0.0030384648,0.0048793587,0.000034676603,0.00016021199,0.00020144398,0.80563736],"genre_scores_gemma":[0.011425217,0.13281153,0.009442331,0.002042171,0.0029913147,0.00007738964,0.0002087875,0.00012055861,0.84088075],"study_design_codex":"theoretical_or_conceptual","study_design_gemma":"not_applicable","domain_scores_codex":[0.99992394,0.000012588773,0.0000029860491,0.000011161122,0.00004071258,0.0000085451165],"domain_scores_gemma":[0.99993265,0.00003633405,0.0000033656345,0.0000052705973,0.00001430297,0.0000081051285],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00015298699,0.00067913736,0.00034233948,0.00074681814,0.00041364445,0.0014634514,0.0006278142,0.0010371375,0.017000046],"category_scores_gemma":[0.00028445583,0.0002169791,0.00023217646,0.0005589371,0.0013227585,0.0014186079,0.00081879104,0.0020510138,0.0070121107],"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":[0.000034384717,0.000038746108,0.00013696922,0.00067834463,0.000008688207,0.00041591053,0.00067711796,0.0010359588,0.0036058032,0.39032844,0.29601187,0.3070277],"study_design_scores_gemma":[0.0000025096767,0.000008478662,0.0002375478,0.0003357816,0.0000025632182,0.000643795,0.00008021899,0.00015356587,0.00024988438,0.06736038,0.93091893,0.0000063923194],"about_ca_topic_score_codex":0.0008837521,"about_ca_topic_score_gemma":0.0020533516,"teacher_disagreement_score":0.017000046,"about_ca_system_score_codex":0.0006243144,"about_ca_system_score_gemma":0.000851773,"threshold_uncertainty_score":0.05687082},"labels":[],"label_agreement":null},{"id":"W2766018790","doi":"10.1016/j.parkreldis.2017.10.017","title":"When shaking during standing points to hereditary spastic paraplegias","year":2017,"lang":"en","type":"letter","venue":"Parkinsonism & Related Disorders","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":6,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Toronto Western Hospital","funders":"","keywords":"Hereditary spastic paraplegia; Medicine; Neuroscience; Spastic; Physical medicine and rehabilitation; Psychology; Phenotype; Biology; Genetics; Cerebral palsy","score_opus":0.02952005036332798,"score_gpt":0.2591431382300225,"score_spread":0.22962308786669453,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2766018790","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":[0.43812382,0.015552587,0.0040492862,0.3175817,0.017752739,0.000322876,0.0010798125,0.000760087,0.20477705],"genre_scores_gemma":[0.9146643,0.003771141,0.0012624195,0.041563418,0.02718111,0.0000495988,0.00023792077,0.0000918484,0.011178249],"study_design_codex":"case_report","study_design_gemma":"case_report","domain_scores_codex":[0.9991472,0.00012169473,0.00015881796,0.00014047779,0.00014996684,0.0002819343],"domain_scores_gemma":[0.996923,0.0010167959,0.0007810767,0.00019776286,0.00060135295,0.00048002947],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00040566118,0.0018127736,0.0011899474,0.0022310098,0.00254784,0.0018588187,0.0015526267,0.0147882,0.005272531],"category_scores_gemma":[0.007824983,0.00061885495,0.0012368226,0.0016188349,0.0017623603,0.0021213354,0.0010347067,0.0074894475,0.0024914145],"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":[0.000089547306,0.000022181452,0.0067850035,0.00007131535,0.00002285736,0.9778651,0.00016768469,0.000082608996,0.0005095179,0.00048874435,0.010376313,0.0035191253],"study_design_scores_gemma":[0.00004438531,0.00007963971,0.012874877,0.00015483858,0.000063945205,0.9782933,0.00048344902,0.00065936963,0.00050782494,0.0017952599,0.005006327,0.000036807665],"about_ca_topic_score_codex":0.006659708,"about_ca_topic_score_gemma":0.009385649,"teacher_disagreement_score":0.0147882,"about_ca_system_score_codex":0.0029300288,"about_ca_system_score_gemma":0.0012203075,"threshold_uncertainty_score":0.02125895},"labels":[],"label_agreement":null},{"id":"W2785699277","doi":"10.1136/jnnp-2017-317562","title":"PFN2 and GAMT as common molecular determinants of axonal Charcot-Marie-Tooth disease","year":2018,"lang":"en","type":"article","venue":"Journal of Neurology Neurosurgery & Psychiatry","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":19,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Western University","funders":"Medical Research Council; Wellcome Trust; Charcot-Marie-Tooth Association","keywords":"Induced pluripotent stem cell; Disease; Blot; Pathogenesis; Biology; Pathophysiology; Motor neuron; Lymphoblast; Medicine; Pathology; Neuroscience; Bioinformatics; Gene; Genetics; Cell culture; Embryonic stem cell","score_opus":0.01898974153659529,"score_gpt":0.28073316051535224,"score_spread":0.26174341897875697,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2785699277","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":[0.9977586,0.0010227399,0.0006844501,0.000043320502,0.000008153666,0.0000073664273,0.00017637257,0.00001888993,0.00028002073],"genre_scores_gemma":[0.99762756,0.0003338733,0.0013652969,0.000040826315,0.0000072570247,0.00001327211,0.0003211823,0.0000072729804,0.00028351866],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.99986243,0.000013456534,0.000011612079,0.000056124423,0.000038231177,0.000018162918],"domain_scores_gemma":[0.9998859,0.000014493709,0.00005150403,0.0000062096306,0.000013935327,0.000027965425],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00021874184,0.0005317238,0.00017974892,0.00046376322,0.00016653666,0.00030895867,0.00016439334,0.0004190235,0.00077415584],"category_scores_gemma":[0.00021030394,0.00010378769,0.00020578146,0.00023394926,0.00028324238,0.00019497238,0.00022538497,0.00027796204,0.00014890208],"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":[0.00073798024,0.00002539517,0.037802953,0.00011960241,0.00004536003,0.0017030766,0.00009182486,0.00015462903,0.95548534,0.00007127484,0.00012697474,0.0036355816],"study_design_scores_gemma":[0.00005870522,0.00069675455,0.628726,0.00006623667,0.00023920309,0.02635761,0.00038058165,0.0029718173,0.3360086,0.00039330818,0.004071214,0.000029992016],"about_ca_topic_score_codex":0.00042315,"about_ca_topic_score_gemma":0.00064343936,"teacher_disagreement_score":0.00077415584,"about_ca_system_score_codex":0.0002386584,"about_ca_system_score_gemma":0.0001251598,"threshold_uncertainty_score":0.0025897622},"labels":[],"label_agreement":null},{"id":"W2789920956","doi":"10.1177/0883073818756680","title":"Association of Early-Onset Spasticity and Risk for Cognitive Impairment With Mutations at Amino Acid 499 in <i>SPAST</i>","year":2018,"lang":"en","type":"review","venue":"Journal of Child Neurology","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":19,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Children's Hospital of Eastern Ontario; University of Ottawa","funders":"","keywords":"Spasticity; Hereditary spastic paraplegia; Medicine; Pediatrics; Spastic; Paraplegia; Age of onset; Cerebral palsy; Physical medicine and rehabilitation; Phenotype; Internal medicine; Genetics; Spinal cord; Psychiatry; Gene; Disease; Biology","score_opus":0.026400587859893916,"score_gpt":0.2911654446120525,"score_spread":0.2647648567521586,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2789920956","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":[0.00045298718,0.9982157,0.00006129135,0.00021052385,0.000077439494,0.0000025903719,0.000021713751,0.0000068262625,0.0009508566],"genre_scores_gemma":[0.0029840348,0.9962709,0.00013686513,0.00012950297,0.00012138351,0.000003856534,0.000042307474,0.0000015511526,0.00030974677],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.9998424,0.000022528622,0.000040880328,0.00003134882,0.000047317248,0.000015491361],"domain_scores_gemma":[0.99964225,0.00016974218,0.000075024975,0.000009062646,0.00007220258,0.00003164076],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00029309298,0.0006711323,0.0010292757,0.0028007857,0.00021238091,0.0005423729,0.0006989567,0.00066416466,0.00230666],"category_scores_gemma":[0.00082624814,0.00015666639,0.00031675052,0.0022559671,0.00042204375,0.00067234196,0.00042784653,0.00074294495,0.0011270709],"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":[0.000103016195,0.000038190734,0.0023587896,0.013845492,0.00014808733,0.0034336096,0.00007729697,0.00019116903,0.0009216852,0.0011285235,0.02515614,0.952598],"study_design_scores_gemma":[0.000055337812,0.00016587063,0.02575162,0.017046008,0.0008367535,0.14255185,0.00030719844,0.00018880203,0.001134949,0.0023846396,0.8095046,0.000072473464],"about_ca_topic_score_codex":0.0013809832,"about_ca_topic_score_gemma":0.0019455493,"teacher_disagreement_score":0.0028007857,"about_ca_system_score_codex":0.00035429397,"about_ca_system_score_gemma":0.00094396947,"threshold_uncertainty_score":0.007716596},"labels":[],"label_agreement":null},{"id":"W2790311764","doi":"10.1002/ajmg.a.38628","title":"A novel homozygous <i>AP4B1</i> mutation in two brothers with AP‐4 deficiency syndrome and ocular anomalies","year":2018,"lang":"en","type":"article","venue":"American Journal of Medical Genetics Part A","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":14,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Université de Montréal; Montreal Neurological Institute and Hospital; Centre Hospitalier Universitaire Sainte-Justine; McGill University","funders":"","keywords":"Microcephaly; Exome sequencing; Mutation; Genetics; Sanger sequencing; Phenotype; Ventriculomegaly; Compound heterozygosity; Biology; Medicine; Gene","score_opus":0.017859639891260427,"score_gpt":0.28259367305149485,"score_spread":0.2647340331602344,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2790311764","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":[0.9927908,0.00081882114,0.0017325735,0.0010341465,0.00017354831,0.00006163325,0.00027024656,0.0001412832,0.0029769733],"genre_scores_gemma":[0.9960471,0.0002928631,0.0013266663,0.00047897003,0.00011181483,0.000016607954,0.00012043206,0.00004052005,0.001565064],"study_design_codex":"case_report","study_design_gemma":"case_report","domain_scores_codex":[0.99947685,0.000044030287,0.00006544878,0.00021197074,0.00011400315,0.000087704175],"domain_scores_gemma":[0.99914587,0.00018603675,0.00021741833,0.000044854572,0.000050014172,0.00035581988],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00024525463,0.0015592559,0.0007855383,0.0012288357,0.0017180796,0.000821207,0.00089088606,0.0024605151,0.0036423753],"category_scores_gemma":[0.0013771147,0.00088907516,0.0007791986,0.0005505762,0.0011250472,0.0007757117,0.0013567229,0.0016383382,0.00071860204],"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":[0.00006017414,0.000053438744,0.010515616,0.00004414875,0.000030175706,0.97440726,0.00076218613,0.000074413154,0.011320662,0.00023284457,0.0004137983,0.0020851858],"study_design_scores_gemma":[0.000024480869,0.000090358306,0.019100003,0.000019218405,0.00004387523,0.9762092,0.00023936006,0.00025023025,0.0025082554,0.0001804706,0.001308985,0.000025554049],"about_ca_topic_score_codex":0.0019978278,"about_ca_topic_score_gemma":0.0018910095,"teacher_disagreement_score":0.0036423753,"about_ca_system_score_codex":0.00053906505,"about_ca_system_score_gemma":0.0004462258,"threshold_uncertainty_score":0.0121849775},"labels":[],"label_agreement":null},{"id":"W2791626023","doi":"10.1097/cnd.0000000000000187","title":"Case of Charcot–Marie–Tooth Type 2C Due to a TRPV4 Gene Mutation With Isolated Sudomotor Autonomic Dysfunction","year":2018,"lang":"en","type":"article","venue":"Journal of Clinical Neuromuscular Disease","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":"Western University; London Health Sciences Centre","funders":"","keywords":"Sudomotor; Medicine; Kinesiology; Gerontology; Family medicine; Internal medicine; Physical therapy","score_opus":0.05744820630411446,"score_gpt":0.3354646152362742,"score_spread":0.27801640893215973,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2791626023","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":[0.9653718,0.0029449654,0.0044868225,0.007963235,0.001287749,0.0003132915,0.0004356064,0.0003413979,0.016855096],"genre_scores_gemma":[0.99358714,0.0004466268,0.0015005892,0.0012794656,0.0011957672,0.000036056546,0.00007341,0.000052599076,0.0018283193],"study_design_codex":"case_report","study_design_gemma":"case_report","domain_scores_codex":[0.9982456,0.00014201154,0.00018330048,0.0005429879,0.00029443073,0.00059177174],"domain_scores_gemma":[0.99527466,0.0018568896,0.00054690894,0.00028620267,0.00031896686,0.0017163008],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00086261064,0.0041157454,0.0028283037,0.004264963,0.0053600185,0.002211281,0.0037180826,0.012132262,0.0043930933],"category_scores_gemma":[0.0068925684,0.0019914072,0.0031511618,0.0027305514,0.0040489906,0.0021006633,0.0033890777,0.0053866906,0.0010122514],"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":[0.000022758328,0.000019154184,0.00052854227,0.000008498848,0.0000050736453,0.9988078,0.00004590076,0.00003442585,0.0002110843,0.00006887373,0.00007798881,0.00016998571],"study_design_scores_gemma":[0.000029509694,0.000061496445,0.0020933861,0.000010015151,0.00001805597,0.99688655,0.000054496133,0.0003248341,0.0001942963,0.00017395295,0.00013699387,0.000016435259],"about_ca_topic_score_codex":0.011135783,"about_ca_topic_score_gemma":0.008647157,"teacher_disagreement_score":0.012132262,"about_ca_system_score_codex":0.0036153314,"about_ca_system_score_gemma":0.002287836,"threshold_uncertainty_score":0.02623123},"labels":[],"label_agreement":null},{"id":"W2808041165","doi":"10.1038/s41436-018-0007-7","title":"Targeted exome analysis identifies the genetic basis of disease in over 50% of patients with a wide range of ataxia-related phenotypes","year":2018,"lang":"en","type":"article","venue":"Genetics in Medicine","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":88,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Ottawa Hospital; Children's Hospital of Eastern Ontario","funders":"National Institute of Neurological Disorders and Stroke","keywords":"Ataxia; Exome sequencing; Exome; Medicine; Etiology; Neurology; Phenotype; Genetics; Human genetics; Bioinformatics; Pathology; Biology; Gene; Psychiatry","score_opus":0.015848099394918273,"score_gpt":0.2512102231868165,"score_spread":0.23536212379189825,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2808041165","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":[0.9930964,0.0015501895,0.0012282619,0.00021919295,0.000016810041,0.000015914,0.0019651449,0.00005949109,0.0018486549],"genre_scores_gemma":[0.9962962,0.0007945661,0.00065260753,0.00016190091,0.000018574612,0.000011013482,0.0014678021,0.000017394255,0.00058008946],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99974805,0.00002914681,0.00003461137,0.00008529973,0.00006427964,0.000038643382],"domain_scores_gemma":[0.99963593,0.00015517753,0.00009324163,0.000036323167,0.000044905766,0.000034428806],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00030090022,0.00054107246,0.00047942402,0.0010338456,0.00028500607,0.00051395723,0.00019337518,0.00064462953,0.0023292832],"category_scores_gemma":[0.0010942197,0.00010709314,0.00038012414,0.0008420793,0.0002619627,0.0002864294,0.00044944012,0.00024263503,0.00045751434],"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":[0.0009996345,0.00011378002,0.6813069,0.00017595707,0.00058544526,0.01626954,0.0005339176,0.0005459972,0.22406623,0.0007795121,0.0034080204,0.071215145],"study_design_scores_gemma":[0.000035948637,0.00015552984,0.9406628,0.00005657807,0.0004192651,0.03007738,0.00030053244,0.00086225476,0.020354604,0.000938057,0.0061164894,0.000020625734],"about_ca_topic_score_codex":0.0008191511,"about_ca_topic_score_gemma":0.0012886721,"teacher_disagreement_score":0.0023292832,"about_ca_system_score_codex":0.00012123504,"about_ca_system_score_gemma":0.0001253215,"threshold_uncertainty_score":0.0077922344},"labels":[],"label_agreement":null},{"id":"W2811013421","doi":"10.1017/cjn.2018.173","title":"P.071 Novel mutations in SPG7 identified from patients with late-onset spasticity","year":2018,"lang":"en","type":"article","venue":"Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques","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":true,"route_about_ca":false,"ca_institutions":"Calgary Laboratory Services","funders":"","keywords":"Hereditary spastic paraplegia; Ataxia; Trinucleotide repeat expansion; Cerebellar ataxia; Exome sequencing; Medicine; Frataxin; Mutation; Genetic testing; Genetics; Spinocerebellar ataxia; Biology; Pathology; Phenotype; Gene; Allele","score_opus":0.04327624653106778,"score_gpt":0.26288824660998117,"score_spread":0.2196120000789134,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2811013421","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":[0.9951687,0.0005064541,0.0013823677,0.00025536004,0.00007767458,0.000060257586,0.00086087576,0.000106477426,0.0015818647],"genre_scores_gemma":[0.9976324,0.00012930343,0.00055389374,0.00021408277,0.00007310459,0.000026394619,0.00063824415,0.00004470478,0.0006878648],"study_design_codex":"case_report","study_design_gemma":"case_report","domain_scores_codex":[0.99976665,0.000021349726,0.000026601858,0.00008207338,0.00006440692,0.000038992344],"domain_scores_gemma":[0.9994272,0.00017006257,0.00012157928,0.000026623733,0.00008336528,0.00017124397],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00014970887,0.0017603207,0.0004788602,0.0012672088,0.00060820754,0.0005339058,0.0005369764,0.0018911517,0.0035972823],"category_scores_gemma":[0.0008407331,0.00026209108,0.00065163395,0.00057850406,0.00058416586,0.00017418705,0.0005746183,0.00076237123,0.0014495784],"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":[0.00081217336,0.00024877247,0.11441497,0.00025071308,0.00014019327,0.7554383,0.001120197,0.000471738,0.10828699,0.0004429789,0.00281016,0.0155627625],"study_design_scores_gemma":[0.00013673246,0.0008399508,0.18674819,0.00010534735,0.00018743302,0.7775596,0.00034347863,0.00188561,0.025676409,0.0006007961,0.0058410554,0.00007551026],"about_ca_topic_score_codex":0.00086771435,"about_ca_topic_score_gemma":0.00081775786,"teacher_disagreement_score":0.0035972823,"about_ca_system_score_codex":0.00031261583,"about_ca_system_score_gemma":0.00023329261,"threshold_uncertainty_score":0.012034118},"labels":[],"label_agreement":null},{"id":"W2884964160","doi":"10.1111/cge.13417","title":"Novel <i>SBF2</i> mutations and clinical spectrum of Charcot‐Marie‐Tooth neuropathy type 4B2","year":2018,"lang":"en","type":"review","venue":"Clinical Genetics","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":11,"is_retracted":false,"has_abstract":true,"route_ca_aff":false,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"","funders":"H2020 European Research Council; Friedrich-Baur-Stiftung; Bundesministerium für Bildung und Forschung; Medical Research Council; Ministerstvo Zdravotnictví Ceské Republiky; Newton Fund; Medical Research Council Canada; Wellcome Trust","keywords":"Glaucoma; Genetic counseling; Genetics; Medicine; Mutation; Age of onset; Disease; Pathology; Biology; Gene; Ophthalmology","score_opus":0.30308881583199165,"score_gpt":0.45391859606339174,"score_spread":0.1508297802314001,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2884964160","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":[0.00033632803,0.9975598,0.00013479589,0.00032655796,0.0001727779,0.0000037037544,0.000029929726,0.000009515608,0.0014266357],"genre_scores_gemma":[0.0019376857,0.9966808,0.00025139027,0.00023617687,0.00019262485,0.000006359485,0.000071875,0.0000029186403,0.0006201625],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.9998406,0.00002129571,0.000040991872,0.00003261223,0.000046625402,0.0000178851],"domain_scores_gemma":[0.99973553,0.000113634684,0.00004543443,0.000008728194,0.00006752102,0.000029076093],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00038268225,0.00077184173,0.0010919439,0.004023086,0.00027423547,0.00074018916,0.00086216815,0.0008176955,0.0025666335],"category_scores_gemma":[0.0006772078,0.00022213576,0.00035298502,0.002436138,0.0004458616,0.0010450926,0.0005356123,0.0011179157,0.0017096585],"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":[0.00007380448,0.00003408363,0.00058476505,0.01462048,0.00009533027,0.0029499542,0.00010082316,0.0002882395,0.0018546155,0.0024724682,0.032807518,0.94411784],"study_design_scores_gemma":[0.000026554397,0.00006095702,0.0030922997,0.005643716,0.00016930955,0.037731327,0.00011372034,0.00009102019,0.0005601378,0.0021176264,0.9503614,0.000031921518],"about_ca_topic_score_codex":0.0010286714,"about_ca_topic_score_gemma":0.0017782468,"teacher_disagreement_score":0.004023086,"about_ca_system_score_codex":0.0005275405,"about_ca_system_score_gemma":0.0009457741,"threshold_uncertainty_score":0.008586228},"labels":[],"label_agreement":null},{"id":"W2886314298","doi":"10.1093/hmg/ddy250","title":"Dystonin-A3 upregulation is responsible for maintenance of tubulin acetylation in a less severe<i>dystonia musculorum</i>mouse model for hereditary sensory and autonomic neuropathy type VI","year":2018,"lang":"en","type":"article","venue":"Human Molecular Genetics","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":9,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Ottawa Hospital; University of Ottawa","funders":"Canadian Institutes of Health Research; Department of Science and Technology, Ministry of Science and Technology, India; Canadian Institute for Advanced Research","keywords":"Biology; Microtubule; Gene isoform; Downregulation and upregulation; Acetylation; Neuroscience; Endocrinology; Cell biology; Genetics; Gene","score_opus":0.05019903484114675,"score_gpt":0.28900054519039603,"score_spread":0.2388015103492493,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2886314298","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":[0.9928843,0.0004977716,0.0016352127,0.0002679969,0.00008935501,0.00007354455,0.0020139306,0.00025880942,0.0022790383],"genre_scores_gemma":[0.98029536,0.00055122626,0.0028572367,0.00022027254,0.000025397607,0.00020217952,0.0024006197,0.00015411299,0.013293608],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9995913,0.000043526536,0.00006176069,0.0001280119,0.00007740907,0.00009794816],"domain_scores_gemma":[0.99956375,0.00002486265,0.00012937177,0.00003064084,0.00003063973,0.00022075466],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00019638645,0.00074841053,0.00039643553,0.0007363977,0.00041033307,0.0005165499,0.0004701143,0.0009949943,0.003914974],"category_scores_gemma":[0.00015582745,0.00035025473,0.00072939316,0.0002567566,0.00055982964,0.0002895794,0.00032616264,0.0015272973,0.0009543093],"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":[0.00024489273,0.000076719705,0.00019808597,0.00003321987,0.0000101463775,0.00016174493,0.000021569815,0.00005247254,0.9986166,0.00012984998,0.0000939037,0.00036083427],"study_design_scores_gemma":[0.00021775329,0.0014605719,0.0214484,0.000054222153,0.000093151946,0.0020233535,0.00019496097,0.002614045,0.96690136,0.0002143023,0.0047480455,0.000029827179],"about_ca_topic_score_codex":0.0018113583,"about_ca_topic_score_gemma":0.0027898161,"teacher_disagreement_score":0.003914974,"about_ca_system_score_codex":0.00066689926,"about_ca_system_score_gemma":0.00035482482,"threshold_uncertainty_score":0.013096929},"labels":[],"label_agreement":null},{"id":"W2887997876","doi":"10.1016/j.ymgme.2018.08.005","title":"Identification of a pathogenic PMP2 variant in a multi-generational family with CMT type 1: Clinical gene panels versus genome-wide approaches to molecular diagnosis","year":2018,"lang":"en","type":"article","venue":"Molecular Genetics and Metabolism","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":18,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Trillium Health Centre","funders":"National Institute of Neurological Disorders and Stroke; National Human Genome Research Institute; National Institutes of Health; Baylor-Hopkins Center for Mendelian Genomics; National Heart, Lung, and Blood Institute; Muscular Dystrophy Association","keywords":"Peripheral neuropathy; Gene; Disease; Genetics; Medicine; Identification (biology); Nerve conduction; Biology; Pathology; Internal medicine; Endocrinology","score_opus":0.16287801654358575,"score_gpt":0.30277600286778766,"score_spread":0.13989798632420192,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2887997876","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":[0.99359715,0.0004567165,0.002334855,0.00063304754,0.000043893455,0.000027560107,0.00066211156,0.0000710301,0.0021736063],"genre_scores_gemma":[0.9980414,0.00016666038,0.0011958336,0.00012439872,0.000039940212,0.000009162136,0.00018398675,0.000017362983,0.00022125393],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9995347,0.00008245141,0.000036597015,0.00018079084,0.00010605748,0.000059404974],"domain_scores_gemma":[0.999238,0.00041361325,0.00013650696,0.000038807135,0.0000675743,0.00010550673],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00059695635,0.0015752037,0.00055837,0.0019918045,0.000884249,0.00094476395,0.0007587279,0.0015200597,0.0032540748],"category_scores_gemma":[0.002638495,0.00032925,0.0005565714,0.0012192351,0.00053827104,0.00041711173,0.0006208151,0.00085480197,0.0004454362],"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":[0.0009213659,0.00017092713,0.62249446,0.00011251842,0.00030979948,0.25431743,0.0010013663,0.0013211922,0.094176576,0.0011231146,0.0021968535,0.021854501],"study_design_scores_gemma":[0.000064517415,0.00030370563,0.5367216,0.0001253864,0.0005769254,0.42924643,0.00065462996,0.0059181056,0.021763774,0.0012953343,0.0032691755,0.000060554892],"about_ca_topic_score_codex":0.0021340603,"about_ca_topic_score_gemma":0.0020272522,"teacher_disagreement_score":0.0032540748,"about_ca_system_score_codex":0.00028381436,"about_ca_system_score_gemma":0.00033096108,"threshold_uncertainty_score":0.0108860135},"labels":[],"label_agreement":null},{"id":"W2892626660","doi":"10.1002/mus.26352","title":"Magnetic resonance imaging of the anterior compartment of the lower leg is a biomarker for weakness, disability, and impaired gait in childhood Charcot–Marie–Tooth disease","year":2018,"lang":"en","type":"article","venue":"Muscle & Nerve","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":17,"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":"Medical Research Council Canada; Muscular Dystrophy Association","keywords":"Magnetic resonance imaging; Gait; Medicine; Weakness; Physical medicine and rehabilitation; Muscle weakness; Intramuscular fat; Gait analysis; Ataxic Gait; Physical therapy; Internal medicine; Anatomy; Radiology; Ataxia","score_opus":0.021603095754919307,"score_gpt":0.25235088763571867,"score_spread":0.23074779188079936,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2892626660","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":[0.99934524,0.00026040687,0.00013669931,0.00001856174,0.0000017052511,0.0000051363218,0.00003716927,0.0000039140828,0.00019118334],"genre_scores_gemma":[0.99875593,0.00021989596,0.000754555,0.000020527983,0.0000070164797,0.000011488281,0.00007117338,0.0000026872417,0.00015674469],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99971956,0.00008770013,0.000029724346,0.000056650137,0.0000753263,0.00003106822],"domain_scores_gemma":[0.99908555,0.00021956969,0.0004969386,0.000019843439,0.00009226706,0.00008590309],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00061741925,0.0003844196,0.0002519565,0.0006562183,0.00017953088,0.00030218586,0.00018034723,0.00030664512,0.0010287267],"category_scores_gemma":[0.0012608063,0.00017813589,0.00012607903,0.00031039913,0.0002954305,0.00023638179,0.00023580552,0.00022222791,0.00013280213],"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":[0.00027745595,0.000075902666,0.9780231,0.00006218328,0.000050578088,0.0007715762,0.0001259445,0.0001242052,0.015248272,0.000016239403,0.00010716933,0.005117407],"study_design_scores_gemma":[0.000006748738,0.00020769336,0.9950263,0.000015893034,0.00002394475,0.0031661184,0.00007200967,0.00013398634,0.0012411728,0.000009301879,0.00009395479,0.0000028277154],"about_ca_topic_score_codex":0.0014097375,"about_ca_topic_score_gemma":0.0029326743,"teacher_disagreement_score":0.0014097375,"about_ca_system_score_codex":0.00020173992,"about_ca_system_score_gemma":0.00015279994,"threshold_uncertainty_score":0.0034413934},"labels":[],"label_agreement":null},{"id":"W2899047922","doi":"10.1002/mgg3.492","title":"Triple A syndrome presenting as complicated hereditary spastic paraplegia","year":2018,"lang":"en","type":"article","venue":"Molecular Genetics & Genomic Medicine","topic":"Hereditary Neurological Disorders","field":"Neuroscience","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":"Université de Sherbrooke; Montreal Neurological Institute and Hospital; University of Toronto; SickKids Foundation; Hospital for Sick Children; McGill University","funders":"Fonds de Recherche du Québec - Santé; Canadian Institutes of Health Research","keywords":"Medicine; Hereditary spastic paraplegia; Exome sequencing; Spasticity; Pediatrics; Nonsense mutation; Paraplegia; Achalasia; Spastic; Mutation; Pathology; Bioinformatics; Internal medicine; Missense mutation; Genetics; Physical therapy; Spinal cord","score_opus":0.03581023620230196,"score_gpt":0.282812790738024,"score_spread":0.24700255453572206,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2899047922","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":[0.9957047,0.000337143,0.0006104661,0.00010186231,0.000016206104,0.00002286504,0.00010493532,0.00003292999,0.0030687517],"genre_scores_gemma":[0.9992337,0.00014051971,0.00028236426,0.00005794227,0.000018391225,0.0000070743877,0.0000695422,0.0000059774175,0.00018449328],"study_design_codex":"case_report","study_design_gemma":"case_report","domain_scores_codex":[0.99985445,0.000015082705,0.000019946934,0.00003984951,0.000035233843,0.000035459252],"domain_scores_gemma":[0.9993173,0.00019621044,0.0001833832,0.000026541311,0.000053005144,0.00022362868],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00011040306,0.0009976076,0.0004297921,0.00096419576,0.00073709444,0.00039960185,0.00024410407,0.0008663032,0.0021930346],"category_scores_gemma":[0.0011126805,0.00024182092,0.00026859602,0.00061881484,0.00050347904,0.0002799514,0.0005977403,0.00046481326,0.00042157632],"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":[0.00016999025,0.00007244802,0.08864957,0.00007054953,0.00005872661,0.88362134,0.00049450836,0.0002450777,0.020709636,0.00033393147,0.0007724597,0.0048016505],"study_design_scores_gemma":[0.000023768072,0.00013361136,0.046256844,0.000023454342,0.000037076148,0.94970095,0.00016075144,0.00042629053,0.0023175012,0.00033947016,0.00056479545,0.000015439138],"about_ca_topic_score_codex":0.0014551821,"about_ca_topic_score_gemma":0.0018766196,"teacher_disagreement_score":0.0021930346,"about_ca_system_score_codex":0.00027522296,"about_ca_system_score_gemma":0.00035392752,"threshold_uncertainty_score":0.0073364377},"labels":[],"label_agreement":null},{"id":"W2903537572","doi":"10.1186/s12883-018-1201-6","title":"A novel nonsense mutation in WNK1/HSN2 associated with sensory neuropathy and limb destruction in four siblings of a large Iranian pedigree","year":2018,"lang":"en","type":"article","venue":"BMC Neurology","topic":"Hereditary Neurological Disorders","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":"Princess Margaret Cancer Centre; University Health Network","funders":"Neuroscience Research Center, Shahid Beheshti University of Medical Sciences; Shahid Beheshti University of Medical Sciences","keywords":"Genetics; Sanger sequencing; Exome sequencing; Nonsense mutation; Mutation; Gene; Nonsense; Allele; Candidate gene; Biology; Medicine; Missense mutation","score_opus":0.05093716382779921,"score_gpt":0.2667312105382462,"score_spread":0.215794046710447,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2903537572","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":[0.99822146,0.00016885667,0.00054360414,0.00012517707,0.000019397261,0.00003484784,0.00011561384,0.000023775134,0.0007472183],"genre_scores_gemma":[0.99858034,0.00009128397,0.0005771085,0.00009931941,0.00001701269,0.000010665162,0.00010695877,0.00001215681,0.0005050638],"study_design_codex":"case_report","study_design_gemma":"case_report","domain_scores_codex":[0.99958676,0.00004946349,0.00003994773,0.00018136666,0.00008593503,0.000056617122],"domain_scores_gemma":[0.99961203,0.000081602586,0.000092882,0.000024660903,0.00005035355,0.00013850204],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00030794585,0.0017095827,0.00051847566,0.0013330684,0.0014583033,0.00045223694,0.0007707605,0.0011216603,0.0018785945],"category_scores_gemma":[0.0010576124,0.00049691,0.00060226687,0.0007273947,0.0008286857,0.00036553567,0.00078697875,0.00064986234,0.00025231275],"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":[0.00025346005,0.00019494079,0.11192251,0.00008163362,0.00013695433,0.85758305,0.0024431895,0.0004433818,0.01957439,0.00036371627,0.0007450223,0.006257804],"study_design_scores_gemma":[0.000057838133,0.0002755351,0.15914111,0.000031733936,0.000109367225,0.8330965,0.000683426,0.00088769884,0.003776015,0.00028348094,0.0016115461,0.00004573724],"about_ca_topic_score_codex":0.004664281,"about_ca_topic_score_gemma":0.006224837,"teacher_disagreement_score":0.004664281,"about_ca_system_score_codex":0.0006503657,"about_ca_system_score_gemma":0.0006067791,"threshold_uncertainty_score":0.009274244},"labels":[],"label_agreement":null},{"id":"W2904333943","doi":"10.3390/ijms19124072","title":"Neuromuscular Junction Changes in a Mouse Model of Charcot-Marie-Tooth Disease Type 4C","year":2018,"lang":"en","type":"article","venue":"International Journal of Molecular Sciences","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":31,"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; Children's Hospital of Eastern Ontario; University of Ottawa","funders":"Medical Research Council; Wellcome Trust; Association Française contre les Myopathies","keywords":"Neuromuscular junction; Biology; Axon; Acetylcholine receptor; Sciatic nerve; Neuroscience; Cell biology; Pathology; Anatomy; Medicine; Genetics; Receptor","score_opus":0.049336510843890354,"score_gpt":0.2984019529560228,"score_spread":0.24906544211213244,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2904333943","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":[0.98575044,0.0021221414,0.0030457124,0.000771086,0.0002934527,0.00040981063,0.0025448836,0.00065574667,0.0044067698],"genre_scores_gemma":[0.9631259,0.0029576656,0.008122712,0.00063960406,0.000074897296,0.0011078089,0.003043333,0.0002940323,0.020634025],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99922574,0.00011963601,0.00009077971,0.0002074149,0.00023263329,0.00012382132],"domain_scores_gemma":[0.99935406,0.00011768261,0.00019105416,0.00006033215,0.00007289352,0.00020387517],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00066151586,0.0015278028,0.0008352467,0.00279154,0.0009747359,0.0007189579,0.0009633601,0.0032840096,0.0040159156],"category_scores_gemma":[0.0005363434,0.0006876909,0.0008599976,0.00073322793,0.0009701539,0.0006375144,0.0006481894,0.002243489,0.0010180809],"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":[0.0010052444,0.0008459817,0.0005885132,0.00014770371,0.000052856387,0.0019467371,0.00014364663,0.00042415847,0.99207884,0.0006047583,0.00048084062,0.0016806427],"study_design_scores_gemma":[0.0010612174,0.008229475,0.03621197,0.00046044303,0.00038784026,0.01009188,0.000553577,0.011785323,0.91196126,0.0014022785,0.017704947,0.00014973264],"about_ca_topic_score_codex":0.0037943781,"about_ca_topic_score_gemma":0.0056411675,"teacher_disagreement_score":0.0040159156,"about_ca_system_score_codex":0.0015715993,"about_ca_system_score_gemma":0.000685672,"threshold_uncertainty_score":0.013434589},"labels":[],"label_agreement":null},{"id":"W2904448294","doi":"10.1212/wnl.0000000000007089","title":"Clinical spectrum of <i>STX1B</i> -related epileptic disorders","year":2019,"lang":"en","type":"article","venue":"Neurology","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":56,"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":"Medical Research Council; Epilepsy Research UK; National Institutes of Health; Canadian Institutes of Health Research; Epilepsy Society; Deutsche Forschungsgemeinschaft; Eberhard Karls Universität Tübingen; European Commission; National Institute of Neurological Disorders and Stroke; Bundesministerium für Bildung und Forschung; National Institute for Health and Care Research; Wellcome Trust; South London and Maudsley NHS Foundation Trust","keywords":"Epilepsy; Epileptic seizure; Genetic data; Phenotype; Electroencephalography; Epilepsy syndromes","score_opus":0.01975686282187357,"score_gpt":0.2770705656045465,"score_spread":0.25731370278267296,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2904448294","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":[0.99630773,0.0005361951,0.0006654683,0.000106954474,0.0000054429156,0.00003150775,0.000224712,0.000028661138,0.0020933002],"genre_scores_gemma":[0.9986821,0.00023348865,0.00047484887,0.00008744458,0.000018401171,0.000012291749,0.0003187585,0.0000089786445,0.00016370253],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.999808,0.000034297474,0.000040940253,0.000046464967,0.00003159408,0.000038733517],"domain_scores_gemma":[0.99973744,0.00008515268,0.00007925153,0.000011604915,0.00003116742,0.000055320783],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0002004283,0.0008634939,0.00033895503,0.0007242178,0.00031294802,0.00022760277,0.00020179323,0.0003446923,0.0025033702],"category_scores_gemma":[0.00079333666,0.0001342782,0.00023214235,0.00044015664,0.0004616248,0.00022259733,0.00057779864,0.0002134762,0.00034834663],"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":[0.0014017442,0.0001589679,0.73711115,0.00027153338,0.00015881228,0.13158713,0.0009600931,0.0007278724,0.091559604,0.0006649968,0.0018654307,0.033532698],"study_design_scores_gemma":[0.00008491936,0.0002654835,0.7635783,0.000052758012,0.00007746092,0.22801073,0.0004308105,0.0005375537,0.00493143,0.00066275813,0.0013504138,0.000017355751],"about_ca_topic_score_codex":0.00087133335,"about_ca_topic_score_gemma":0.00096802204,"teacher_disagreement_score":0.0025033702,"about_ca_system_score_codex":0.00016166137,"about_ca_system_score_gemma":0.00022976859,"threshold_uncertainty_score":0.008374572},"labels":[],"label_agreement":null},{"id":"W2905433528","doi":"10.1016/j.ejmg.2018.12.010","title":"CAPN1 mutations: Expanding the CAPN1-related phenotype: From hereditary spastic paraparesis to spastic ataxia","year":2018,"lang":"en","type":"article","venue":"European Journal of Medical Genetics","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":25,"is_retracted":false,"has_abstract":false,"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; University of Alberta","funders":"","keywords":"Genetics; Ataxia; Hereditary spastic paraplegia; Exome sequencing; Biology; Mutation; Cerebellar ataxia; Phenotype; Gene; Neuroscience","score_opus":0.04061558287012854,"score_gpt":0.2835356355710399,"score_spread":0.24292005270091135,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2905433528","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":[0.9795687,0.0031593745,0.002543855,0.0011011185,0.00019289483,0.00007690107,0.0007612448,0.00017849912,0.0124174375],"genre_scores_gemma":[0.99372333,0.0012864866,0.0020564105,0.00038642183,0.00021640297,0.00002034129,0.00047018696,0.00004656425,0.0017937641],"study_design_codex":"case_report","study_design_gemma":"observational","domain_scores_codex":[0.99983335,0.000017087812,0.00002638973,0.00005009749,0.000040973555,0.000032117845],"domain_scores_gemma":[0.99972457,0.00006407077,0.000071948896,0.000019022516,0.00004262851,0.00007767024],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00018069388,0.0013957429,0.0006063574,0.0008582539,0.0005542189,0.00040627862,0.00057349715,0.0013402088,0.0027960553],"category_scores_gemma":[0.0008650318,0.0002025925,0.00041942194,0.0008372228,0.00053779926,0.00040929834,0.0006773985,0.0005606846,0.0008063106],"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":[0.0014393952,0.00024106378,0.044456463,0.0006600482,0.00018120305,0.6191805,0.0010379713,0.0026977365,0.24229476,0.0028582662,0.008386379,0.07656624],"study_design_scores_gemma":[0.00019380316,0.00035402304,0.15130286,0.00023767007,0.00038323872,0.77882636,0.00032931552,0.0038623202,0.04426117,0.0036059334,0.016548062,0.00009519009],"about_ca_topic_score_codex":0.002125574,"about_ca_topic_score_gemma":0.0025210045,"teacher_disagreement_score":0.0027960553,"about_ca_system_score_codex":0.00044821925,"about_ca_system_score_gemma":0.00044989274,"threshold_uncertainty_score":0.009353757},"labels":[],"label_agreement":null},{"id":"W2906189405","doi":"10.21466/ac.usncpia.2015","title":"Ultrasound‐guided sciatic nerve catheter placement in a patient with Charcot‐Marie‐Tooth disease","year":2015,"lang":"en","type":"article","venue":"Anaesthesia Cases","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":false,"ca_institutions":"St. Michael's Hospital","funders":"","keywords":"Medicine; Tooth disease; Sciatic nerve; Context (archaeology); Surgery; Peripheral neuropathy; Catheter; Anesthesia; Disease; Pathology","score_opus":0.05311665484975571,"score_gpt":0.2614341770958409,"score_spread":0.20831752224608518,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2906189405","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":[0.9795314,0.00298979,0.003061555,0.0034274189,0.00025560678,0.00008028494,0.00011383564,0.00018531755,0.010354741],"genre_scores_gemma":[0.9958216,0.00071812735,0.0011800465,0.0007793489,0.00024329072,0.000014999409,0.000038080158,0.000019463841,0.001185099],"study_design_codex":"case_report","study_design_gemma":"case_report","domain_scores_codex":[0.9994868,0.00006707376,0.00006724239,0.00010149677,0.00012442206,0.00015302203],"domain_scores_gemma":[0.99797136,0.0008008831,0.00036815283,0.00008332654,0.00011387996,0.00066233927],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0003238774,0.0011488972,0.0006753692,0.0020925885,0.002015723,0.000971652,0.0011462289,0.0039748326,0.0018059374],"category_scores_gemma":[0.0031612061,0.00067713065,0.0007778187,0.0011849779,0.0015150914,0.0009964894,0.0009758064,0.0026557962,0.0005928628],"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":[0.000016117077,0.000039531024,0.0031005275,0.000015240798,0.000004226832,0.99522984,0.00015837551,0.000078739955,0.0005537615,0.000070600894,0.00011136353,0.00062176114],"study_design_scores_gemma":[0.0000045187376,0.0000920413,0.0027150875,0.00001113232,0.000007300489,0.9963701,0.0000699279,0.00021783276,0.00030893323,0.000048797527,0.00014743378,0.000006937931],"about_ca_topic_score_codex":0.003993444,"about_ca_topic_score_gemma":0.004780387,"teacher_disagreement_score":0.003993444,"about_ca_system_score_codex":0.0012448409,"about_ca_system_score_gemma":0.0010599227,"threshold_uncertainty_score":0.009032011},"labels":[],"label_agreement":null},{"id":"W2906759100","doi":"10.1016/j.parkreldis.2018.12.031","title":"Beyond dystonia and ataxia: Expanding the phenotype of SQSTM1 mutations","year":2019,"lang":"en","type":"article","venue":"Parkinsonism & Related Disorders","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":25,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Ontario Brain Institute; Toronto Western Hospital; University of Toronto","funders":"","keywords":"Dystonia; Ataxia; Phenotype; Genetics; Medicine; Neuroscience; Physical medicine and rehabilitation; Biology; Gene","score_opus":0.010277700961143017,"score_gpt":0.23730605010732544,"score_spread":0.22702834914618242,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2906759100","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":[0.9565664,0.011620252,0.005056569,0.0033306219,0.00023011588,0.000055250355,0.00067335385,0.00027279105,0.022194704],"genre_scores_gemma":[0.9842122,0.008002141,0.004620445,0.00064068736,0.0002955477,0.000014153088,0.00042248258,0.000050714618,0.0017416218],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9998605,0.000017733717,0.000024744266,0.000032754422,0.000038150945,0.000025977388],"domain_scores_gemma":[0.9997571,0.000074720534,0.00003631292,0.000019522007,0.000044920293,0.00006732706],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00022095158,0.0008901805,0.0006615414,0.0011941401,0.00032698584,0.0005418373,0.00044440178,0.0010027369,0.0021261284],"category_scores_gemma":[0.0004566536,0.00013380121,0.0005038809,0.000616971,0.0008303326,0.0009398893,0.000984952,0.00063068507,0.00042076892],"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":[0.0010753779,0.00031630244,0.07065519,0.001081387,0.00015710996,0.17468005,0.0022159978,0.0028407609,0.50885075,0.011903018,0.008288535,0.21793556],"study_design_scores_gemma":[0.00018880954,0.0011515858,0.30283457,0.00091280654,0.00051716575,0.5296013,0.0013609335,0.008817936,0.04878288,0.027681665,0.077976495,0.00017387158],"about_ca_topic_score_codex":0.0027015603,"about_ca_topic_score_gemma":0.004386306,"teacher_disagreement_score":0.0027015603,"about_ca_system_score_codex":0.00045116222,"about_ca_system_score_gemma":0.0005755531,"threshold_uncertainty_score":0.0071126223},"labels":[],"label_agreement":null},{"id":"W2909283569","doi":"10.1101/524793","title":"Direct binding of the flexible C-terminal segment of periaxin to β4 integrin suggests a molecular basis for CMT4F","year":2019,"lang":"en","type":"preprint","venue":"bioRxiv (Cold Spring Harbor Laboratory)","topic":"Hereditary Neurological Disorders","field":"Neuroscience","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":"Discovery Centre","funders":"Biocenter, University of Oulu; Norges Forskningsråd; Universitetet i Bergen; Wellcome Trust; European Synchrotron Radiation Facility; Deutsches Elektronen-Synchrotron","keywords":"Basal lamina; Cell biology; Dystroglycan; Cytoplasm; Fibronectin; Schwann cell; Integrin; Biology; Cytoskeleton; Myelin; Cell; Extracellular matrix; Laminin; Biochemistry; Anatomy; Neuroscience; Ultrastructure; Central nervous system","score_opus":0.025436805956168183,"score_gpt":0.2509257884791723,"score_spread":0.22548898252300412,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2909283569","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":[0.97843367,0.0011651381,0.00902979,0.00081036234,0.00012654265,0.000027593192,0.00038655265,0.000107968066,0.009912367],"genre_scores_gemma":[0.9883387,0.00023179344,0.003967001,0.00017663471,0.00002367761,0.000020209067,0.0007016465,0.000018949353,0.00652129],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9999205,0.000005970315,0.0000028539596,0.000027371985,0.000018636207,0.000024685034],"domain_scores_gemma":[0.99993455,0.000013075195,0.000015110636,0.0000075362873,0.000006258106,0.000023374101],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00009756216,0.00022609977,0.00010663193,0.00014301133,0.00033673042,0.00021665641,0.00022899458,0.00051432184,0.005047423],"category_scores_gemma":[0.00013718121,0.000082708655,0.0002501238,0.000094929106,0.00029631707,0.00019780248,0.00020827414,0.0004931126,0.0007694514],"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":[0.00009458407,0.000014916715,0.00053841574,0.000030415298,0.0000061436162,0.0005324481,0.000019284416,0.00008368792,0.9959194,0.0011069004,0.00024079639,0.0014128883],"study_design_scores_gemma":[0.000043121345,0.00012019474,0.031054033,0.000011770319,0.000012419161,0.0030229879,0.00009161599,0.0036576027,0.9515789,0.0010863277,0.0093072755,0.000013778231],"about_ca_topic_score_codex":0.00086281786,"about_ca_topic_score_gemma":0.0009805332,"teacher_disagreement_score":0.005047423,"about_ca_system_score_codex":0.0003408824,"about_ca_system_score_gemma":0.00015610943,"threshold_uncertainty_score":0.01688528},"labels":[],"label_agreement":null},{"id":"W2910767355","doi":"10.1038/s41439-018-0036-4","title":"A new case of spastic paraplegia type 64 due to a missense mutation in the ENTPD1 gene","year":2019,"lang":"en","type":"article","venue":"Human Genome Variation","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":14,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Atlantic Cancer Research Institute; Université de Moncton; Dr. Georges-L.-Dumont University Hospital Centre","funders":"","keywords":"Hereditary spastic paraplegia; Missense mutation; Proband; Sanger sequencing; Genetics; Mutation; Medicine; Gene; Disease; Paraplegia; Phenotype; Bioinformatics; Biology; Pathology; Spinal cord","score_opus":0.03978937865315921,"score_gpt":0.2759837326748396,"score_spread":0.2361943540216804,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2910767355","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":[0.9963697,0.0004303362,0.00088300515,0.00030408034,0.00006364631,0.000037407215,0.00011722369,0.000048027916,0.0017465706],"genre_scores_gemma":[0.9985,0.00015119993,0.00041733208,0.00012599443,0.00006762227,0.0000074715135,0.000056868284,0.000011577272,0.0006619375],"study_design_codex":"case_report","study_design_gemma":"case_report","domain_scores_codex":[0.99967015,0.000032943743,0.000035953537,0.00012811238,0.000049436305,0.00008333475],"domain_scores_gemma":[0.99929774,0.00023165754,0.00014610248,0.000053990276,0.00005441466,0.00021605936],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00021210246,0.0013293523,0.00076859456,0.0014170241,0.0014841937,0.0005563579,0.0005821876,0.0017964357,0.0023271535],"category_scores_gemma":[0.0014206073,0.00065615895,0.00071222504,0.0007320791,0.0010551614,0.00039152466,0.0010210746,0.0009385282,0.00041289354],"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":[0.00004326395,0.000043865537,0.006552204,0.000020817071,0.000015988166,0.9884942,0.00030616697,0.000042795687,0.003173162,0.00008747831,0.00014749517,0.0010725171],"study_design_scores_gemma":[0.00002123963,0.00011101072,0.017239455,0.000011495966,0.00003287168,0.98024863,0.000116651645,0.0002754907,0.0012365087,0.00012506207,0.0005691877,0.000012365453],"about_ca_topic_score_codex":0.0027191343,"about_ca_topic_score_gemma":0.0027591009,"teacher_disagreement_score":0.0027191343,"about_ca_system_score_codex":0.00058697205,"about_ca_system_score_gemma":0.00033933413,"threshold_uncertainty_score":0.007785082},"labels":[],"label_agreement":null},{"id":"W2913027812","doi":"10.1002/ana.25426","title":"Variation in <i>SIPA1L2</i> is correlated with phenotype modification in Charcot– Marie– Tooth disease type 1A","year":2019,"lang":"en","type":"article","venue":"Annals of Neurology","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":45,"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; National Institute of Neurological Disorders and Stroke; Medical Research Council; National Institutes of Health; Medical Research Council Canada; Eunice Kennedy Shriver National Institute of Child Health and Human Development; University College London; National Institute for Health and Care Research; Muscular Dystrophy Association; Charcot-Marie-Tooth Association","keywords":"Gene knockdown; Chromatin immunoprecipitation; Immunoprecipitation; Phenotype; Genetics; Genetic variation; Biology; Copy-number variation; Gene; Gene expression; Medicine; Molecular biology; Genome","score_opus":0.06774442585708847,"score_gpt":0.2941810837806736,"score_spread":0.22643665792358514,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2913027812","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":[0.99842095,0.0001587234,0.00041371371,0.000043722015,0.000009465518,0.00000650073,0.00064544554,0.000022615053,0.0002786889],"genre_scores_gemma":[0.99862516,0.00005508098,0.0004097155,0.000047446603,0.0000115578605,0.000011398016,0.0005088851,0.000021432797,0.00030939747],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9996661,0.00005555241,0.000034977442,0.00015738429,0.00005822136,0.00002765181],"domain_scores_gemma":[0.9994597,0.0001228865,0.0002669183,0.000036083387,0.000034302433,0.000080107035],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00031040062,0.000513704,0.00029829584,0.00081254664,0.00033898882,0.00035896618,0.0002878856,0.0004673521,0.0028592872],"category_scores_gemma":[0.0005936105,0.00015341282,0.00036734852,0.00067171623,0.00026974958,0.00009884158,0.00030086178,0.0004302065,0.00042569565],"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":[0.0041011805,0.00023738756,0.51621705,0.00016381234,0.00087449147,0.005215931,0.0005022059,0.0011081645,0.45662722,0.0003517015,0.0015687802,0.0130320685],"study_design_scores_gemma":[0.00004997212,0.00021493265,0.98193836,0.000021527532,0.0001766658,0.0058111344,0.00009977667,0.0017177459,0.008748803,0.00014406959,0.0010554725,0.000021623953],"about_ca_topic_score_codex":0.00092023687,"about_ca_topic_score_gemma":0.00097048125,"teacher_disagreement_score":0.0028592872,"about_ca_system_score_codex":0.00017169247,"about_ca_system_score_gemma":0.00007624274,"threshold_uncertainty_score":0.009565294},"labels":[],"label_agreement":null},{"id":"W2913966243","doi":"10.1002/humu.23000","title":"High Frequency of Pathogenic Rearrangements in <i>SPG11</i> and Extensive Contribution of Mutational Hotspots and Founder Alleles","year":2016,"lang":"en","type":"article","venue":"Human Mutation","topic":"Hereditary Neurological Disorders","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":"University of Toronto; Hospital for Sick Children; SickKids Foundation","funders":"Deutsche Forschungsgemeinschaft","keywords":"Biology; Genetics; Allele; Hereditary spastic paraplegia; Haplotype; Breakpoint; Phenotype; Non-allelic homologous recombination; Founder effect; Gene; Recombination; Chromosome; Genetic recombination","score_opus":0.027450150340376123,"score_gpt":0.267140986140143,"score_spread":0.23969083579976685,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2913966243","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":[0.9989009,0.00016360947,0.00042375253,0.000015075335,0.0000026013472,0.000007554115,0.00007391989,0.000015594247,0.00039699228],"genre_scores_gemma":[0.99940586,0.00006570114,0.00029434316,0.000011390773,0.000006201525,0.000004380608,0.000110512345,0.000005804852,0.00009577537],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.99964106,0.00006300016,0.000035202243,0.00013455436,0.00008141389,0.000044837532],"domain_scores_gemma":[0.99966514,0.000097286764,0.00010227469,0.00005521248,0.000026820537,0.000053304684],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00027878667,0.00035401323,0.00034290567,0.0012580563,0.0002907809,0.00035679524,0.00023401933,0.00042046537,0.001743016],"category_scores_gemma":[0.0007407138,0.0001639633,0.00019440435,0.0005289483,0.0004415386,0.00015728697,0.00036810577,0.00029525533,0.00026170732],"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":[0.0005850982,0.000074678,0.48036295,0.000071681854,0.0002081371,0.005424926,0.00067004963,0.0003168116,0.48451617,0.0003756556,0.00030958885,0.027084222],"study_design_scores_gemma":[0.000018314402,0.00018415907,0.9590436,0.00001712582,0.000097644355,0.02161881,0.0002378745,0.0005728302,0.01680899,0.0003349971,0.0010497317,0.000015845184],"about_ca_topic_score_codex":0.00046798823,"about_ca_topic_score_gemma":0.0009107271,"teacher_disagreement_score":0.001743016,"about_ca_system_score_codex":0.00013591563,"about_ca_system_score_gemma":0.00009729838,"threshold_uncertainty_score":0.005831003},"labels":[],"label_agreement":null},{"id":"W2914530644","doi":"10.1080/01677063.2019.1566326","title":"High diagnostic yield and novel variants in very late-onset spasticity","year":2019,"lang":"en","type":"article","venue":"Journal of Neurogenetics","topic":"Hereditary Neurological Disorders","field":"Neuroscience","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":"University of Calgary","funders":"","keywords":"Cohort; Genetic testing; Genetics; Genotype; Biology; Phenotype; Mutation; DNA sequencing; Medicine; Internal medicine; Gene","score_opus":0.03316971865219483,"score_gpt":0.24022642137156758,"score_spread":0.20705670271937276,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2914530644","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":[0.99741447,0.0003094173,0.0015570307,0.000079828984,0.000010419942,0.000008448133,0.00012304352,0.00003326352,0.00046400484],"genre_scores_gemma":[0.99887556,0.000069606096,0.0007898643,0.000027433312,0.000012833478,0.000004455068,0.0001371379,0.0000084677895,0.000074623975],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99900633,0.00028087886,0.0001092939,0.00022222503,0.00024126073,0.00014000568],"domain_scores_gemma":[0.99700004,0.0017340626,0.00046146597,0.00022881046,0.00031238317,0.00026323972],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0007718035,0.00037546776,0.00042052567,0.0012115315,0.00032728803,0.0006695272,0.00043498553,0.0007808257,0.0010389304],"category_scores_gemma":[0.004964833,0.00019091526,0.00022379907,0.00042856557,0.00038811585,0.0002656603,0.0005852016,0.00039624207,0.00045680942],"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":[0.00073252403,0.000089276975,0.85631317,0.00006606619,0.00006235867,0.022719335,0.0005985818,0.0003793443,0.08863094,0.00032413602,0.00055255124,0.029531721],"study_design_scores_gemma":[0.00005344917,0.000519436,0.8044705,0.000048984748,0.00014556882,0.14354785,0.00062107167,0.0028108351,0.043264065,0.0012634104,0.0031932641,0.000061539155],"about_ca_topic_score_codex":0.00026511072,"about_ca_topic_score_gemma":0.00035023034,"teacher_disagreement_score":0.0012115315,"about_ca_system_score_codex":0.00016150052,"about_ca_system_score_gemma":0.00010829227,"threshold_uncertainty_score":0.004081726},"labels":[],"label_agreement":null},{"id":"W2920596348","doi":"10.1007/s11910-019-0930-2","title":"Update on the Genetics of Spastic Paraplegias","year":2019,"lang":"en","type":"review","venue":"Current Neurology and Neuroscience Reports","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":120,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"SickKids Foundation; Hospital for Sick Children","funders":"","keywords":"Spasticity; Hereditary spastic paraplegia; Neuroscience; TARDBP; Genetic heterogeneity; Mechanism (biology); Biology; Spastic; Molecular genetics; Medicine; Bioinformatics; Gene; Phenotype; Genetics; SOD1; Psychiatry","score_opus":0.21162522847625484,"score_gpt":0.3735518811796069,"score_spread":0.16192665270335208,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2920596348","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":[0.00006827746,0.9969676,0.00012810047,0.00071062456,0.0012011414,0.0000034088525,0.00003700943,0.00001062939,0.00087308005],"genre_scores_gemma":[0.0004352498,0.99543923,0.0002603782,0.0009601996,0.0020555314,0.0000052239957,0.00008831852,0.0000022850213,0.0007536097],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.999668,0.000069812755,0.0000708434,0.00004933508,0.00010733649,0.000034701072],"domain_scores_gemma":[0.998871,0.00069058477,0.00011703437,0.000025121944,0.00021168067,0.000084479456],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00095950183,0.0011823385,0.0020857798,0.004160193,0.0002521711,0.0013691279,0.0013458334,0.001852419,0.004772302],"category_scores_gemma":[0.0017835967,0.00037098257,0.0007057492,0.003018819,0.00053599,0.0017055025,0.00088433624,0.0021600781,0.0023642324],"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":[0.00012074214,0.000058767953,0.00039955732,0.012879486,0.00020861017,0.0013049071,0.00006697822,0.0004173053,0.0011765535,0.002524974,0.18673222,0.7941098],"study_design_scores_gemma":[0.000037082504,0.000049406593,0.00096859934,0.005275017,0.00031271673,0.0034390953,0.000051146282,0.00007953189,0.00012647158,0.0014529335,0.9881825,0.000025555868],"about_ca_topic_score_codex":0.0016082611,"about_ca_topic_score_gemma":0.0037981654,"teacher_disagreement_score":0.004772302,"about_ca_system_score_codex":0.00074669754,"about_ca_system_score_gemma":0.001386905,"threshold_uncertainty_score":0.015964925},"labels":[],"label_agreement":null},{"id":"W2926679006","doi":"10.1007/s00439-019-02003-x","title":"Canine neuropathies: powerful spontaneous models for human hereditary sensory neuropathies","year":2019,"lang":"en","type":"review","venue":"Human Genetics","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":15,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Université de Montréal","funders":"Agence Nationale de la Recherche","keywords":"Biology; Human genetics; Genetic heterogeneity; Disease; Gene; Inbreeding; Human Pathology; Genetics; Pathology; Phenotype; Population; Medicine","score_opus":0.18176841424850418,"score_gpt":0.34817031347895616,"score_spread":0.16640189923045198,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2926679006","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":[0.00016058201,0.99788046,0.0003069115,0.00019618729,0.00017392224,0.0000057423986,0.0000420694,0.0000146889215,0.0012194221],"genre_scores_gemma":[0.0010532202,0.9973074,0.00038346957,0.00019942444,0.00016948984,0.000010675832,0.00010126841,0.0000029515465,0.0007720327],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.9998066,0.000033994387,0.000028825303,0.00004329106,0.000063220956,0.000024115263],"domain_scores_gemma":[0.9996283,0.00018609215,0.000045001198,0.000016510616,0.00007448377,0.000049511],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0008868737,0.0013960606,0.0015539253,0.0025030144,0.00026510717,0.0012708168,0.001225174,0.0014440865,0.001967476],"category_scores_gemma":[0.00065601326,0.0003183915,0.00044425562,0.001661692,0.0008821565,0.0012544445,0.0008540981,0.0024346078,0.001667291],"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":[0.00018607931,0.00013098834,0.000253882,0.012663733,0.000102024336,0.00064069964,0.000059994,0.00058567367,0.0052288244,0.008913708,0.054594778,0.9166395],"study_design_scores_gemma":[0.000037842663,0.00009953018,0.00061612186,0.0019140757,0.00014998857,0.0022348734,0.000043945256,0.00010812454,0.00093601533,0.0028866131,0.99094534,0.000027388429],"about_ca_topic_score_codex":0.000981285,"about_ca_topic_score_gemma":0.0021092992,"teacher_disagreement_score":0.0025030144,"about_ca_system_score_codex":0.0008441898,"about_ca_system_score_gemma":0.0007524825,"threshold_uncertainty_score":0.0065819025},"labels":[],"label_agreement":null},{"id":"W2934013272","doi":"10.1093/hmg/ddz060","title":"Loss of Cajal bodies in motor neurons from patients with novel mutations in VRK1","year":2019,"lang":"en","type":"article","venue":"Human Molecular Genetics","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":35,"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":"Seventh Framework Programme; Agence Universitaire de la Francophonie; French Muscular Dystrophy Association","keywords":"Biology; Neurite; Phenotype; Motor neuron; Induced pluripotent stem cell; Cell biology; Neuroscience; Genetics; Gene; Spinal cord","score_opus":0.020032109217923595,"score_gpt":0.2411134202414444,"score_spread":0.2210813110235208,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2934013272","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":[0.99874014,0.00029022514,0.00034989792,0.000047973746,0.00000587663,0.000007632832,0.00010546292,0.000034960176,0.00041791704],"genre_scores_gemma":[0.9988689,0.00012776164,0.00046922997,0.00003426402,0.0000064874603,0.0000040513323,0.00011793504,0.000010688203,0.00036084317],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9998292,0.000010239185,0.000028270406,0.00007525902,0.00003266605,0.000024372102],"domain_scores_gemma":[0.99979526,0.00003921225,0.00007505978,0.000012446109,0.000018853776,0.00005922505],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0001117546,0.00076658314,0.00037730343,0.0006202757,0.00044256073,0.0003607047,0.00025326986,0.0005070461,0.0013495365],"category_scores_gemma":[0.00045120955,0.00019772252,0.00023239039,0.00020137247,0.00047789258,0.00017077652,0.00043208993,0.000382439,0.00018683012],"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":[0.000810222,0.00011919564,0.11570373,0.00023873564,0.00017376672,0.1434457,0.0013505702,0.00042111083,0.7213626,0.00036826744,0.00039610514,0.015609971],"study_design_scores_gemma":[0.000108218155,0.00047418044,0.45929205,0.000044946275,0.0002172454,0.47057462,0.00037827325,0.0011949728,0.064887606,0.0002367074,0.002547331,0.000043922897],"about_ca_topic_score_codex":0.0025272113,"about_ca_topic_score_gemma":0.0034252242,"teacher_disagreement_score":0.0025272113,"about_ca_system_score_codex":0.0003102151,"about_ca_system_score_gemma":0.000261912,"threshold_uncertainty_score":0.005025029},"labels":[],"label_agreement":null},{"id":"W2934716016","doi":"10.1016/j.ajhg.2019.03.001","title":"Truncating Mutations in UBAP1 Cause Hereditary Spastic Paraplegia","year":2019,"lang":"en","type":"article","venue":"The American Journal of Human Genetics","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":62,"is_retracted":false,"has_abstract":false,"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; McMaster University","funders":"National Institute of Neurological Disorders and Stroke; National Institutes of Health; Horizon 2020; Instituto de Salud Carlos III; Universiteit Antwerpen; Federación Española de Enfermedades Raras; Bundesministerium für Bildung und Forschung; Morris Animal Foundation","keywords":"Hereditary spastic paraplegia; Paraplegia; Spastic; Medicine; Physical medicine and rehabilitation; Mutation; Genetics; Biology; Spinal cord; Phenotype; Cerebral palsy; Gene; Psychiatry","score_opus":0.03804177151817558,"score_gpt":0.29728175144228774,"score_spread":0.2592399799241122,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2934716016","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":[0.9931393,0.0008308967,0.001172433,0.00028694325,0.00011584228,0.00003416352,0.00074344635,0.00011910409,0.0035579165],"genre_scores_gemma":[0.99766123,0.00020918265,0.0005995796,0.00009449034,0.000048620444,0.0000109345265,0.0002373553,0.000024250701,0.0011143845],"study_design_codex":"case_report","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99981993,0.000025294015,0.000036453403,0.00003530275,0.000047773367,0.00003519394],"domain_scores_gemma":[0.9995554,0.000103617036,0.00016693184,0.000025604442,0.000032025608,0.00011632701],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00015696409,0.0014019335,0.00062799046,0.0010861875,0.00076513697,0.00034157743,0.0006013084,0.0013114567,0.0032085807],"category_scores_gemma":[0.0006428935,0.0002516048,0.00044430498,0.00090511265,0.000715588,0.00022468441,0.00082916324,0.0006343585,0.00079981715],"study_design_candidate":"bench_or_experimental","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.002514085,0.0005623464,0.05582824,0.00046986964,0.0005603907,0.46060216,0.00087157823,0.0025167756,0.43845394,0.0034175385,0.0051989127,0.029004106],"study_design_scores_gemma":[0.00036519676,0.0009357702,0.34451157,0.00020064914,0.00083396444,0.5276361,0.00064613536,0.0072639817,0.10109965,0.003749179,0.012604681,0.00015311937],"about_ca_topic_score_codex":0.0017612937,"about_ca_topic_score_gemma":0.0022845468,"teacher_disagreement_score":0.0032085807,"about_ca_system_score_codex":0.00046689523,"about_ca_system_score_gemma":0.00033516635,"threshold_uncertainty_score":0.010733783},"labels":[],"label_agreement":null},{"id":"W2943035376","doi":"10.3747/co.26.4491","title":"Treatment-Induced Remission of Medulloblastoma Using a Chemotherapeutic Regimen Devoid of Vincristine in a Child with Charcot–Marie–Tooth Disease","year":2019,"lang":"en","type":"article","venue":"Current Oncology","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":4,"is_retracted":false,"has_abstract":true,"route_ca_aff":false,"route_ca_fund":false,"route_ca_venue":true,"route_about_ca":false,"ca_institutions":"","funders":"","keywords":"Medicine; Vincristine; Medulloblastoma; Regimen; Disease; Peripheral neuropathy; Population; Surgery; Oncology; Internal medicine; Chemotherapy; Pathology; Cyclophosphamide; Endocrinology","score_opus":0.10496131150394805,"score_gpt":0.3653456305390537,"score_spread":0.26038431903510567,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2943035376","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":[0.98987377,0.00237628,0.0015229562,0.0018405468,0.00013072812,0.00010542949,0.00018721423,0.00011473429,0.003848291],"genre_scores_gemma":[0.99505603,0.001662103,0.0011407767,0.000490229,0.000066339395,0.0000231958,0.00016320913,0.000031091196,0.0013670867],"study_design_codex":"case_report","study_design_gemma":"case_report","domain_scores_codex":[0.9998499,0.000018518693,0.000018134893,0.000031342537,0.00003762668,0.00004447329],"domain_scores_gemma":[0.9996784,0.000060199687,0.00006999408,0.000019929028,0.000020312502,0.0001513166],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00011056531,0.00043889074,0.0004709786,0.000552726,0.0008087056,0.0002546857,0.00048047028,0.0009098224,0.00042153796],"category_scores_gemma":[0.00071366987,0.00023618918,0.0004980265,0.00033978425,0.0006013322,0.00028339904,0.00038824318,0.0015208168,0.00016158663],"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":[0.00028758458,0.00040022624,0.020702833,0.00017076157,0.000056283483,0.93265307,0.00086233753,0.00088571646,0.019445306,0.0008185408,0.00089386397,0.022823505],"study_design_scores_gemma":[0.00013736403,0.0022663076,0.080691814,0.00008702948,0.00012542948,0.89595634,0.00028634307,0.0018595358,0.012235039,0.00029953627,0.0060159545,0.00003942585],"about_ca_topic_score_codex":0.0083543565,"about_ca_topic_score_gemma":0.021957867,"teacher_disagreement_score":0.0083543565,"about_ca_system_score_codex":0.0012191741,"about_ca_system_score_gemma":0.0009233139,"threshold_uncertainty_score":0.016611457},"labels":[],"label_agreement":null},{"id":"W2944851696","doi":"10.3389/fneur.2019.00508","title":"Are Cognitive Changes in Hereditary Spastic Paraplegias Restricted to Complicated Forms?","year":2019,"lang":"en","type":"article","venue":"Frontiers in Neurology","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":21,"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":"Hospital de Clínicas de Porto Alegre; Conselho Nacional de Desenvolvimento Científico e Tecnológico; Ministério da Ciência, Tecnologia e Inovação; Fundação de Amparo à Pesquisa do Estado do Rio Grande do Sul; Coordenação de Aperfeiçoamento de Pessoal de Nível Superior; Fundação Instituto de Pesquisas Econômicas; Fundação de Amparo à Pesquisa do Estado de São Paulo","keywords":"Hereditary spastic paraplegia; Cognition; Medicine; Spastic; Neuroscience; Physical medicine and rehabilitation; Psychology; Genetics; Biology; Phenotype; Cerebral palsy","score_opus":0.03076072824684653,"score_gpt":0.2582095960633248,"score_spread":0.22744886781647825,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2944851696","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":[0.99891174,0.00040000762,0.000060751714,0.000038687944,0.0000038559,0.000005538994,0.00005997423,0.000005366233,0.00051407126],"genre_scores_gemma":[0.99959797,0.00016429281,0.00004227484,0.00002304299,0.000019809133,0.0000034461052,0.00008837671,0.0000016043615,0.000059265],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.999574,0.00008009482,0.00006570098,0.00011052039,0.00010345919,0.00006629299],"domain_scores_gemma":[0.9977539,0.0005276866,0.0012118979,0.00013094292,0.0001745873,0.00020090716],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00039909343,0.0006197654,0.0005716449,0.0016916035,0.0003922087,0.000589345,0.0005357073,0.00074226345,0.0034353193],"category_scores_gemma":[0.00382789,0.00029366638,0.0002701928,0.0010585533,0.0011540431,0.00054318487,0.0006295656,0.00026641233,0.00038469527],"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":[0.00043440628,0.000057162946,0.9845792,0.000063424646,0.000099158504,0.0057297354,0.0002562699,0.00007674574,0.00094224163,0.000053283606,0.00013071185,0.0075776866],"study_design_scores_gemma":[0.000012731203,0.00017585797,0.9837562,0.000020357174,0.000046062225,0.015247003,0.00022336277,0.00011334695,0.00010373959,0.00014158495,0.00015452909,0.0000051242373],"about_ca_topic_score_codex":0.0014981213,"about_ca_topic_score_gemma":0.0015098131,"teacher_disagreement_score":0.0034353193,"about_ca_system_score_codex":0.00020977246,"about_ca_system_score_gemma":0.0002563303,"threshold_uncertainty_score":0.011492252},"labels":[],"label_agreement":null},{"id":"W2954503239","doi":"10.1186/s13023-019-1138-x","title":"Thiemann disease and familial digital arthropathy – brachydactyly: two sides of the same coin?","year":2019,"lang":"en","type":"review","venue":"Orphanet Journal of Rare Diseases","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":8,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"SickKids Foundation; Hospital for Sick Children; University of Toronto","funders":"Hospital for Sick Children","keywords":"Brachydactyly; Medicine; Second toe; Dermatology; Genetics; Anatomy; Biology; Pediatrics","score_opus":0.0434923029663481,"score_gpt":0.2991151008054097,"score_spread":0.2556227978390616,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2954503239","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":[0.45418495,0.52619207,0.0010345635,0.00799708,0.0005024698,0.000026928386,0.0002937994,0.00005323321,0.009714926],"genre_scores_gemma":[0.8690154,0.12454303,0.0013411406,0.002497067,0.0009903366,0.000020247713,0.0003414152,0.000012495161,0.0012388197],"study_design_codex":"case_report","study_design_gemma":"not_applicable","domain_scores_codex":[0.9995443,0.000070689275,0.000105737745,0.000096876734,0.00010627871,0.000076136224],"domain_scores_gemma":[0.99828964,0.0008052335,0.0006718648,0.00003904231,0.00009120754,0.00010302703],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0005052822,0.00026907402,0.00080814323,0.0017305863,0.00038329052,0.0008052894,0.00040112773,0.0014804369,0.0032426866],"category_scores_gemma":[0.0023465022,0.00020789537,0.00041506227,0.0027744926,0.0012254675,0.0012773265,0.0006049711,0.0007773494,0.00048259803],"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":[0.0010633514,0.0001323381,0.3971795,0.005957993,0.00056497357,0.4182365,0.0024263654,0.00023609489,0.008704437,0.0072883666,0.007927448,0.15028259],"study_design_scores_gemma":[0.00009012581,0.00013895072,0.16645773,0.0032570108,0.00047667776,0.7974235,0.0016663524,0.00022887003,0.0008992032,0.0046033454,0.024694698,0.00006353879],"about_ca_topic_score_codex":0.0011603732,"about_ca_topic_score_gemma":0.001123427,"teacher_disagreement_score":0.0032426866,"about_ca_system_score_codex":0.00028469894,"about_ca_system_score_gemma":0.00044138817,"threshold_uncertainty_score":0.010847926},"labels":[],"label_agreement":null},{"id":"W2954973013","doi":"","title":"Caracterização do perfil cognitivo e deglutição nas paraparesias espásticas hereditárias","year":2018,"lang":"pt","type":"dissertation","venue":"LA Referencia (Red Federada de Repositorios Institucionales de Publicaciones Científicas)","topic":"Hereditary Neurological Disorders","field":"Neuroscience","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":"Psychology","score_opus":0.03473712976190453,"score_gpt":0.27531636436714063,"score_spread":0.24057923460523611,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2954973013","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":[0.996786,0.0019105189,0.00021693873,0.0001161134,0.0000057772645,0.00001639756,0.00015680026,0.0000069980942,0.00078447483],"genre_scores_gemma":[0.9986488,0.00069367536,0.00019752416,0.000047999652,0.000005985129,0.000010733279,0.00011107291,0.0000016310382,0.0002826458],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9995053,0.00014315269,0.0000561773,0.00010981227,0.00009216851,0.000093461524],"domain_scores_gemma":[0.9983224,0.0002849885,0.00076734606,0.00007867715,0.00040308273,0.00014344272],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0010035201,0.00049084285,0.0004124156,0.0012440545,0.00042026,0.0011669169,0.00034264443,0.000422021,0.0013379648],"category_scores_gemma":[0.0028310835,0.00018790974,0.00033685146,0.0012474824,0.00061183225,0.0005367898,0.00058281224,0.00032940257,0.00015403666],"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":[0.00016856083,0.0000573162,0.98546636,0.00015575909,0.000088718305,0.00083042606,0.00091971515,0.00006793937,0.0021733914,0.00007827803,0.000098750475,0.009894685],"study_design_scores_gemma":[0.0000054061593,0.00027048474,0.9954196,0.00010894315,0.00010348453,0.0017027297,0.0009223239,0.00013560198,0.0006894993,0.00010703875,0.00052631355,0.0000086486625],"about_ca_topic_score_codex":0.018830191,"about_ca_topic_score_gemma":0.01940238,"teacher_disagreement_score":0.018830191,"about_ca_system_score_codex":0.0007315243,"about_ca_system_score_gemma":0.0009413823,"threshold_uncertainty_score":0.037441134},"labels":[],"label_agreement":null},{"id":"W2957491009","doi":"10.1136/bcr-2018-228956","title":"Successful treatment of nasopharyngeal cancer using radiotherapy with concurrent cetuximab in a patient with Charcot-Marie-Tooth disease","year":2019,"lang":"en","type":"article","venue":"BMJ Case Reports","topic":"Hereditary Neurological Disorders","field":"Neuroscience","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":"London Health Sciences Centre; Western University","funders":"","keywords":"Cetuximab; Medicine; Nasopharyngeal carcinoma; Radiation therapy; Context (archaeology); Disease; Neurotoxicity; Regimen; Chemotherapy; Oncology; Cancer; Internal medicine; Toxicity; Colorectal cancer","score_opus":0.03381924662449765,"score_gpt":0.3114426453035686,"score_spread":0.27762339867907093,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2957491009","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":[0.97679025,0.0052776155,0.0028905033,0.0035155725,0.00027184575,0.00010435765,0.000098061304,0.00014594186,0.010905764],"genre_scores_gemma":[0.9934422,0.0016168511,0.0021001333,0.00070045615,0.00017941177,0.000021014996,0.000042030417,0.00002465074,0.0018733169],"study_design_codex":"case_report","study_design_gemma":"case_report","domain_scores_codex":[0.9997509,0.000029948877,0.000029252153,0.00006786142,0.00004982013,0.000072280694],"domain_scores_gemma":[0.99966705,0.00007473376,0.000071097005,0.000029725477,0.000025868412,0.0001315237],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0002079047,0.0006615417,0.0006148885,0.0006761688,0.002018643,0.00071467,0.00065534614,0.0025414748,0.00083145016],"category_scores_gemma":[0.0011645971,0.00041925584,0.0007802641,0.00047944486,0.0008491372,0.0006375114,0.00076843245,0.0014473503,0.00039195077],"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":[0.000040568844,0.00004794486,0.0035069352,0.000028293916,0.000011552287,0.9894517,0.0002053275,0.00017770781,0.002343914,0.00012702846,0.00018638706,0.0038726572],"study_design_scores_gemma":[0.000011580616,0.00010238515,0.0032612605,0.000013403217,0.000024896468,0.99300534,0.00008579527,0.0004065365,0.0018806072,0.000116914474,0.0010784044,0.000012822255],"about_ca_topic_score_codex":0.0034107976,"about_ca_topic_score_gemma":0.007466539,"teacher_disagreement_score":0.0034107976,"about_ca_system_score_codex":0.0010409922,"about_ca_system_score_gemma":0.0010546106,"threshold_uncertainty_score":0.0075529814},"labels":[],"label_agreement":null},{"id":"W2962105967","doi":"10.1002/ana.25524","title":"<i>PDXK</i> mutations cause polyneuropathy responsive to pyridoxal 5′‐phosphate supplementation","year":2019,"lang":"en","type":"article","venue":"Annals of Neurology","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":75,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Newborn Screening Ontario; Ottawa Hospital; Children's Hospital of Eastern Ontario; University of Ottawa","funders":"Medical Research Council; Canadian Institutes of Health Research; Rosetrees Trust; University College London; Great Ormond Street Hospital for Children; King's College London; Genome British Columbia; Ontario Genomics Institute; Brain Research UK; Genome Alberta; Ataxia UK; National Institute for Health and Care Research; Ontario Genomics; NIHR Biomedical Research Centre, Royal Marsden NHS Foundation Trust/Institute of Cancer Research; Genome Canada; Muscular Dystrophy UK; Wellcome Trust","keywords":"Polyneuropathy; Compound heterozygosity; Enzyme replacement therapy; Biology; Pyridoxal; B vitamins; Biochemistry; Mutation; Medicine; Genetics; Internal medicine; Gene; Endocrinology; Enzyme; Disease","score_opus":0.07800025178566969,"score_gpt":0.3451750341943346,"score_spread":0.2671747824086649,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2962105967","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":[0.99559194,0.00038573344,0.0009873189,0.00024464793,0.000019290785,0.000032860826,0.00020595684,0.00008986859,0.0024422668],"genre_scores_gemma":[0.9978886,0.0001531337,0.0009112235,0.00014459579,0.000020827185,0.000013224949,0.000119264405,0.000017001863,0.0007320875],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9998784,0.00001755868,0.000016272143,0.000037470905,0.000029402616,0.000020808538],"domain_scores_gemma":[0.9998386,0.000041588424,0.000057983318,0.0000071182176,0.000018322506,0.000036349382],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00014466941,0.0008795982,0.0002865354,0.00021860277,0.00031614924,0.0002349617,0.0001960454,0.00044522987,0.0020752817],"category_scores_gemma":[0.00030890887,0.00015198707,0.0001981942,0.00019747288,0.0003596943,0.00010735632,0.000220944,0.00033733883,0.00037436423],"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":[0.0018059582,0.0002060052,0.08204463,0.0003301559,0.00018683737,0.116111025,0.0004570419,0.000836266,0.77646905,0.0004875736,0.0020253218,0.019040046],"study_design_scores_gemma":[0.00037630473,0.0015917715,0.48397103,0.00015046356,0.00040016882,0.31724122,0.00038422327,0.0037251224,0.18388769,0.0005686494,0.0076578283,0.000045475703],"about_ca_topic_score_codex":0.001377978,"about_ca_topic_score_gemma":0.0018486873,"teacher_disagreement_score":0.0020752817,"about_ca_system_score_codex":0.00033976225,"about_ca_system_score_gemma":0.000168908,"threshold_uncertainty_score":0.0069425106},"labels":[],"label_agreement":null},{"id":"W2962973340","doi":"10.3233/jnd-190404","title":"A Novel Mutation in MARS in a Patient with Charcot-Marie-Tooth Disease, Axonal, Type 2U with Congenital Onset","year":2019,"lang":"en","type":"article","venue":"Journal of Neuromuscular Diseases","topic":"Hereditary Neurological Disorders","field":"Neuroscience","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":"Children's Hospital of Eastern Ontario; University of Ottawa","funders":"National Institute of Neurological Disorders and Stroke; Ontario Genomics Institute; National Institute of General Medical Sciences; Canadian Institutes of Health Research; Ontario Genomics; Genome Canada","keywords":"Tooth disease; Exome sequencing; Disease; Medicine; Phenotype; Age of onset; Exome; Genetics; Mutation; Gene; Genetic heterogeneity; Biology; Pathology","score_opus":0.01616984490172923,"score_gpt":0.22671385155959467,"score_spread":0.21054400665786543,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2962973340","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":[0.99442,0.0005278539,0.0012393134,0.0007365774,0.00011159321,0.00006002849,0.0003329627,0.00010776736,0.0024639238],"genre_scores_gemma":[0.99704725,0.00014742695,0.0011292809,0.00027714882,0.000080056474,0.000014890558,0.000095269635,0.000020615022,0.0011879934],"study_design_codex":"case_report","study_design_gemma":"case_report","domain_scores_codex":[0.9996736,0.000026611206,0.000034999357,0.000138502,0.000060786802,0.000065484004],"domain_scores_gemma":[0.9994537,0.00020072405,0.0000884859,0.000020610083,0.00003163869,0.00020473941],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00024759237,0.0013226244,0.000791645,0.0011415086,0.0013681902,0.0005899393,0.0007896131,0.003515141,0.0021780492],"category_scores_gemma":[0.0014298108,0.0004585526,0.0007042449,0.0007043241,0.0010223463,0.0005700402,0.0008149535,0.0010548673,0.0005357775],"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":[0.00010558785,0.000049576553,0.004742239,0.000036956353,0.000012493896,0.9821797,0.0004692818,0.00014272607,0.009575325,0.00025717757,0.00028520005,0.0021437341],"study_design_scores_gemma":[0.000031209143,0.0002456724,0.022119718,0.000017701337,0.000029076089,0.97219974,0.00015779844,0.0006717418,0.0034419692,0.00025821093,0.00079517585,0.000032025753],"about_ca_topic_score_codex":0.002854929,"about_ca_topic_score_gemma":0.003143831,"teacher_disagreement_score":0.003515141,"about_ca_system_score_codex":0.0005302515,"about_ca_system_score_gemma":0.00046275815,"threshold_uncertainty_score":0.0072862506},"labels":[],"label_agreement":null},{"id":"W2964220319","doi":"10.3389/fneur.2019.00859","title":"Gangliosides: Treatment Avenues in Neurodegenerative Disease","year":2019,"lang":"en","type":"review","venue":"Frontiers in Neurology","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":116,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Women and Children’s Health Research Institute; University of Alberta; University of Saskatchewan","funders":"Canadian Institutes of Health Research; Ministry of Public Safety and Security; Huntington Society of Canada; Fondation Brain Canada","keywords":"Medicine; Clinical trial; Disease; Ganglioside; Placebo; Internal medicine; Pathology","score_opus":0.10788885803120916,"score_gpt":0.3372801490285808,"score_spread":0.2293912909973716,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2964220319","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":[0.002867765,0.9807734,0.00066196796,0.009875935,0.00087259937,0.000032486583,0.00009443389,0.000038604863,0.004782686],"genre_scores_gemma":[0.023352245,0.96363264,0.002057382,0.005652141,0.0020937736,0.0000842291,0.00016843835,0.000013829717,0.002945417],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.9997141,0.00011474419,0.000032218035,0.00004039413,0.00006617253,0.00003245614],"domain_scores_gemma":[0.99952054,0.00018888804,0.00008850751,0.000023555262,0.00010724934,0.00007127108],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.001410865,0.000466859,0.0008954113,0.0008655075,0.00023952399,0.0009696997,0.0005439659,0.0011985872,0.0068535632],"category_scores_gemma":[0.0010200489,0.000101283775,0.00065457524,0.0007213307,0.00049493124,0.0012002119,0.0007102438,0.0019931062,0.0014409663],"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":[0.0013423348,0.000517304,0.0007545235,0.007743475,0.00020857106,0.0002743888,0.00015683511,0.00032909593,0.0049303416,0.013333204,0.02668549,0.9437246],"study_design_scores_gemma":[0.0015213707,0.0033357656,0.0055398885,0.008921108,0.00063959806,0.0010521227,0.0003222447,0.0005905465,0.0029819198,0.028160216,0.94687444,0.000060815546],"about_ca_topic_score_codex":0.00071081705,"about_ca_topic_score_gemma":0.0022404972,"teacher_disagreement_score":0.0068535632,"about_ca_system_score_codex":0.00058414246,"about_ca_system_score_gemma":0.00092882063,"threshold_uncertainty_score":0.022927403},"labels":[],"label_agreement":null},{"id":"W2971491823","doi":"10.3389/fncel.2019.00419","title":"Going Too Far Is the Same as Falling Short†: Kinesin-3 Family Members in Hereditary Spastic Paraplegia","year":2019,"lang":"en","type":"review","venue":"Frontiers in Cellular Neuroscience","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":82,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Simon Fraser University","funders":"Japan Society for the Promotion of Science; Natural Sciences and Engineering Research Council of Canada; Simon Fraser University","keywords":"Kinesin; Hereditary spastic paraplegia; Biology; Microtubule; Cell biology; Neuroscience; Axoplasmic transport; Motor neuron; Spinocerebellar ataxia; Golgi apparatus; Endoplasmic reticulum; Genetics; Gene; Ataxia; Phenotype; Spinal cord","score_opus":0.08880426727474568,"score_gpt":0.3044871330831105,"score_spread":0.21568286580836482,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2971491823","genre_codex":"commentary","genre_gemma":"review","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"review","genre_consensus":null,"domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.094768085,0.19641499,0.0060906005,0.45967302,0.10916446,0.00008521689,0.003250009,0.0012521694,0.1293014],"genre_scores_gemma":[0.4134387,0.08843291,0.004786774,0.15483357,0.020834016,0.00011252229,0.0024501642,0.00068934605,0.31442195],"study_design_codex":"not_applicable","study_design_gemma":"not_applicable","domain_scores_codex":[0.99955374,0.00007184589,0.000057797773,0.0001029084,0.0001273333,0.000086280874],"domain_scores_gemma":[0.9993813,0.000076703,0.0000887908,0.000023525672,0.00021943725,0.00021018075],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0005511974,0.0005926608,0.00052994245,0.0007432508,0.0017868154,0.0011607956,0.0004660966,0.0017708441,0.018578097],"category_scores_gemma":[0.0011388693,0.00011349859,0.00034061473,0.00088625954,0.0010178025,0.0017203907,0.0010851708,0.0022716075,0.007497037],"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":[0.0005250616,0.000100943245,0.015808765,0.0007150159,0.00012274187,0.0047513354,0.0015808261,0.00012152936,0.007599331,0.013549476,0.6777805,0.2773445],"study_design_scores_gemma":[0.00003516728,0.00012796081,0.030354628,0.00080904696,0.00011288744,0.020116137,0.0016773567,0.00014501838,0.0015367105,0.010704575,0.93430936,0.00007111118],"about_ca_topic_score_codex":0.0062935688,"about_ca_topic_score_gemma":0.008042989,"teacher_disagreement_score":0.018578097,"about_ca_system_score_codex":0.0011287911,"about_ca_system_score_gemma":0.0011634579,"threshold_uncertainty_score":0.062149882},"labels":[],"label_agreement":null},{"id":"W2972587176","doi":"10.1038/s10038-019-0669-2","title":"SPTAN1 variants as a potential cause for autosomal recessive hereditary spastic paraplegia","year":2019,"lang":"en","type":"article","venue":"Journal of Human Genetics","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":20,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"McGill University Health Centre; McGill Genome Centre; Université Laval; Montreal Neurological Institute and Hospital; McGill University","funders":"Canadian Institutes of Health Research; Government of Canada","keywords":"Hereditary spastic paraplegia; Genetics; Biology; Phenotype; Gene; In silico; Genetic heterogeneity","score_opus":0.035111057638010174,"score_gpt":0.29471172116724853,"score_spread":0.2596006635292384,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2972587176","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":[0.989597,0.0015953435,0.0016091221,0.00090924767,0.00020607057,0.00004501538,0.00069121964,0.00010382493,0.005242981],"genre_scores_gemma":[0.9977331,0.00022706855,0.0008072174,0.00014873012,0.00012053886,0.000008103041,0.00025417088,0.000021792688,0.0006792741],"study_design_codex":"case_report","study_design_gemma":"observational","domain_scores_codex":[0.99956137,0.00007450456,0.000071389644,0.0001096648,0.00011239901,0.0000707072],"domain_scores_gemma":[0.9990765,0.00033799378,0.00029427392,0.000055069722,0.000092611,0.00014351262],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0003153966,0.0018539046,0.00066068734,0.0021072447,0.00095553487,0.0006629261,0.0011496865,0.0022289485,0.0057941484],"category_scores_gemma":[0.00219509,0.00028940605,0.00076959364,0.0013815279,0.00080707896,0.0003518399,0.0007095125,0.0008841172,0.00080290984],"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":[0.0010238015,0.00015735251,0.10458078,0.00020779189,0.00030864854,0.8395994,0.00059340225,0.00081175106,0.038615607,0.0024463271,0.0017491574,0.009905962],"study_design_scores_gemma":[0.00023761179,0.00044620628,0.14438796,0.00027975492,0.0009658519,0.82175916,0.00064111606,0.0062369546,0.014597094,0.0035093313,0.006844006,0.00009486609],"about_ca_topic_score_codex":0.0014594481,"about_ca_topic_score_gemma":0.0013398795,"teacher_disagreement_score":0.0057941484,"about_ca_system_score_codex":0.0003716702,"about_ca_system_score_gemma":0.00040550207,"threshold_uncertainty_score":0.019383311},"labels":[],"label_agreement":null},{"id":"W2977727807","doi":"10.1016/j.jbmt.2019.09.009","title":"An adapted dance program for children with Charcot-Marie-Tooth disease: An exploratory study","year":2019,"lang":"en","type":"article","venue":"Journal of Bodywork and Movement Therapies","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":9,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Shriners Hospitals for Children - Canada; Université de Montréal; Université du Québec à Montréal; Centre Hospitalier Universitaire Sainte-Justine","funders":"","keywords":"Tooth disease; Dance; Exploratory research; Psychology; Medicine; Gerontology; Disease; Art; Visual arts; Sociology; Anthropology; Pathology","score_opus":0.021337359705731713,"score_gpt":0.2735303035588127,"score_spread":0.252192943853081,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2977727807","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":[0.99862504,0.00005364798,0.00008340115,0.000022431088,0.000007854657,0.0007100032,0.00007703966,0.000004531258,0.00041601234],"genre_scores_gemma":[0.9919829,0.0003892149,0.0027410935,0.00011099449,0.000030687956,0.003280204,0.00044326423,0.000010129953,0.0010115565],"study_design_codex":"nonrandomized_trial","study_design_gemma":"qualitative","domain_scores_codex":[0.9986614,0.00039904795,0.00010949983,0.00026304243,0.00021330143,0.00035360365],"domain_scores_gemma":[0.99923694,0.00018841622,0.00008111413,0.00008101881,0.00010342292,0.0003091772],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0012571095,0.0012567987,0.0013258979,0.0013573334,0.0027337787,0.00058485416,0.0010973796,0.0011834905,0.0018388578],"category_scores_gemma":[0.0018598514,0.00040243284,0.0012392021,0.0011050517,0.00077107677,0.00050062354,0.0012070898,0.0011680619,0.000242561],"study_design_candidate":"qualitative","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":[0.020990914,0.5630393,0.15213427,0.0021020877,0.00076339307,0.008526131,0.024288906,0.0026549548,0.013744231,0.0005445344,0.00096281123,0.21024854],"study_design_scores_gemma":[0.021872228,0.26303858,0.6764884,0.00033384882,0.00097044103,0.0022504355,0.025798362,0.0012904542,0.002665132,0.00027720068,0.004815621,0.00019933237],"about_ca_topic_score_codex":0.017617589,"about_ca_topic_score_gemma":0.037473287,"teacher_disagreement_score":0.017617589,"about_ca_system_score_codex":0.0021460382,"about_ca_system_score_gemma":0.0035962758,"threshold_uncertainty_score":0.035030067},"labels":[],"label_agreement":null},{"id":"W2979502004","doi":"10.14740/jnr.v9i4-5.547","title":"Update on an Asian Indian Family With Apparent Autosomal Recessive Charcot-Marie-Tooth Disease Caused by a Mutation in the HSPB1 Gene","year":2019,"lang":"en","type":"article","venue":"Journal of Neurology Research","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":0,"is_retracted":false,"has_abstract":true,"route_ca_aff":false,"route_ca_fund":false,"route_ca_venue":true,"route_about_ca":false,"ca_institutions":"","funders":"","keywords":"Genetics; Genotyping; Mutation; Medicine; Exome sequencing; Gene; Tooth disease; Genetic heterogeneity; Founder effect; Phenotype; Population; Biology; Genotype; Haplotype","score_opus":0.05457369855566343,"score_gpt":0.34183268109746445,"score_spread":0.28725898254180104,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2979502004","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":[0.59585047,0.22665791,0.012077901,0.03685923,0.006602807,0.00026949676,0.0049490575,0.0021378929,0.11459524],"genre_scores_gemma":[0.7757006,0.15863866,0.012267595,0.023362866,0.008962587,0.00008038847,0.003843436,0.00031820964,0.016825635],"study_design_codex":"case_report","study_design_gemma":"case_report","domain_scores_codex":[0.99971765,0.000030566986,0.00007340363,0.000046506655,0.00008902362,0.000042827476],"domain_scores_gemma":[0.9994012,0.00018728443,0.00007997259,0.00003920831,0.00021993816,0.000072476396],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00038141606,0.0008233998,0.00065971614,0.0023058983,0.000622208,0.0009207215,0.00086434674,0.0009010874,0.0023717654],"category_scores_gemma":[0.0010399399,0.0002383937,0.00053454866,0.001205291,0.00032467104,0.00067073334,0.0004603827,0.000834322,0.00072800915],"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":[0.00041658207,0.00018381927,0.07151103,0.0021279873,0.00044053476,0.5396735,0.0030507054,0.00057713746,0.037031196,0.0011376243,0.06949637,0.27435365],"study_design_scores_gemma":[0.000030678304,0.00013285784,0.0708349,0.0008274292,0.0013061664,0.7032924,0.0013523741,0.0005015743,0.0074778595,0.0010444708,0.21311711,0.000082193874],"about_ca_topic_score_codex":0.0050256257,"about_ca_topic_score_gemma":0.010745372,"teacher_disagreement_score":0.0050256257,"about_ca_system_score_codex":0.00055730395,"about_ca_system_score_gemma":0.00055321376,"threshold_uncertainty_score":0.009992719},"labels":[],"label_agreement":null},{"id":"W2981356272","doi":"10.1016/j.jbmt.2019.10.014","title":"Massage therapy treatment and outcomes in a patient with Charcot-Marie-Tooth disease: A case report","year":2019,"lang":"en","type":"article","venue":"Journal of Bodywork and Movement Therapies","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":4,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"MacEwan University","funders":"","keywords":"Medicine; Massage; Lumbar; Physical therapy; Weakness; Range of motion; Myofascial release; Physical medicine and rehabilitation; Manual therapy; Surgery","score_opus":0.016387019032995956,"score_gpt":0.2448629804932145,"score_spread":0.22847596146021854,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2981356272","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":[0.9900333,0.0024995613,0.00059077254,0.0014718751,0.000115414485,0.000041875166,0.00016991579,0.000036163776,0.0050411387],"genre_scores_gemma":[0.9965313,0.00097407895,0.00039965654,0.00036197598,0.00025103445,0.000012287263,0.00013000525,0.000013352741,0.0013264065],"study_design_codex":"case_report","study_design_gemma":"case_report","domain_scores_codex":[0.9996519,0.000031254105,0.00005039476,0.00008318666,0.000058580106,0.0001245713],"domain_scores_gemma":[0.99935585,0.00017393123,0.00014697606,0.000031944004,0.000047054928,0.00024419074],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00018034206,0.0007722493,0.00085944624,0.0013608717,0.0029058272,0.0015447241,0.00086696766,0.0037240714,0.002041719],"category_scores_gemma":[0.0015369377,0.0005028546,0.0012039904,0.0011051312,0.0011469864,0.0009373182,0.0010371938,0.0019132902,0.0006298414],"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":[0.000075655975,0.0002376335,0.02120667,0.000017852213,0.000017737442,0.97543406,0.0002791196,0.00008222582,0.0007023345,0.00009749447,0.00018426609,0.0016649476],"study_design_scores_gemma":[0.000013685339,0.00017182973,0.022319356,0.00001698741,0.00004178968,0.9760267,0.00036192025,0.00026408088,0.00025706168,0.00014340696,0.00035577238,0.000027332711],"about_ca_topic_score_codex":0.0042122244,"about_ca_topic_score_gemma":0.0043133013,"teacher_disagreement_score":0.0042122244,"about_ca_system_score_codex":0.0012660247,"about_ca_system_score_gemma":0.00076711405,"threshold_uncertainty_score":0.009185672},"labels":[],"label_agreement":null},{"id":"W2989796894","doi":"10.1007/s00256-019-03341-7","title":"Highlights of the special scientific sessions of the 46th Annual Scientific Meeting of the International Skeletal Society (ISS) 2019, Vancouver, Canada","year":2019,"lang":"en","type":"review","venue":"Skeletal Radiology","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":0,"is_retracted":false,"has_abstract":false,"route_ca_aff":false,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":true,"ca_institutions":"","funders":"","keywords":"Medicine; Orthopedic surgery; Library science; Family medicine; Medical education; Medical physics; Surgery","score_opus":0.028068623910907607,"score_gpt":0.27231732991646984,"score_spread":0.24424870600556223,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2989796894","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":[0.00036149114,0.7730121,0.00035387473,0.019125301,0.1917764,0.00013004612,0.0005291926,0.00005005593,0.01466165],"genre_scores_gemma":[0.0028146338,0.8007697,0.00069222786,0.009595351,0.13229659,0.00011085504,0.001272814,0.00003847568,0.052409317],"study_design_codex":"not_applicable","study_design_gemma":"not_applicable","domain_scores_codex":[0.99924845,0.00008943666,0.00006965666,0.00009044415,0.00034357008,0.00015839523],"domain_scores_gemma":[0.997343,0.00024481377,0.0001820105,0.000029421177,0.0013006903,0.00090009876],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0022079665,0.0015089306,0.0018175029,0.0032173789,0.0008517669,0.0024278655,0.0014759641,0.0022897108,0.023963926],"category_scores_gemma":[0.0022878065,0.0002956635,0.00084915257,0.0018013032,0.0005992519,0.0012317894,0.0016076587,0.0026185776,0.007705955],"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":[0.0001176223,0.00004270728,0.0001193822,0.00238658,0.00003484982,0.00014564459,0.000028869697,0.000099302706,0.0005157493,0.0006463199,0.8873875,0.1084754],"study_design_scores_gemma":[0.000027141,0.00004618161,0.00094197044,0.0011593017,0.000049813985,0.00029674018,0.00004089326,0.00004541103,0.00012132264,0.00032523062,0.9969324,0.000013646936],"about_ca_topic_score_codex":0.015257417,"about_ca_topic_score_gemma":0.049868196,"teacher_disagreement_score":0.023963926,"about_ca_system_score_codex":0.0026559252,"about_ca_system_score_gemma":0.006390261,"threshold_uncertainty_score":0.08016735},"labels":[],"label_agreement":null},{"id":"W2991318353","doi":"10.1186/s13054-019-2659-3","title":"Translational medicine between human and veterinary emergency and critical care medicine: a story meant to have a happy ending","year":2019,"lang":"en","type":"editorial","venue":"Critical Care","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":3,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Calgary","funders":"","keywords":"Medicine; Alternative medicine; Translational medicine; Hospital medicine; Human medicine; Veterinary medicine; Family medicine; Emergency medicine; Traditional medicine; Pathology","score_opus":0.09351218178317938,"score_gpt":0.40540163304473104,"score_spread":0.31188945126155165,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2991318353","genre_codex":"editorial","genre_gemma":"editorial","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"editorial","genre_consensus":"editorial","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.000019396135,0.002176967,0.00010868449,0.033528853,0.9633958,0.000006862249,0.0000118626485,0.000026737836,0.00072484877],"genre_scores_gemma":[0.0002862324,0.0017404057,0.000104099345,0.01377075,0.980162,0.000008289015,0.000008709326,0.00002101438,0.0038985026],"study_design_codex":"not_applicable","study_design_gemma":"not_applicable","domain_scores_codex":[0.9890619,0.0028575745,0.0011223607,0.0010620006,0.0052051614,0.00069098786],"domain_scores_gemma":[0.92604274,0.028594015,0.0030942773,0.0018999864,0.02705484,0.0133140525],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.014518357,0.0031910874,0.003222187,0.0037871087,0.004579004,0.012110217,0.0039750044,0.022933085,0.015409026],"category_scores_gemma":[0.054996163,0.0012367489,0.0020494217,0.0013217479,0.0039544324,0.0053144256,0.002647879,0.025214218,0.010129336],"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":[0.00002657697,0.000012741145,0.000024996652,0.0001894449,0.000016400756,0.00013770007,0.000027785754,0.000016275144,0.000040804185,0.0004735508,0.9949809,0.0040528676],"study_design_scores_gemma":[0.00007147556,0.000041193933,0.00022129925,0.00064928504,0.0000505406,0.00039819584,0.00016831065,0.0001925632,0.00008613856,0.0024237323,0.99566454,0.000032729233],"about_ca_topic_score_codex":0.0014866677,"about_ca_topic_score_gemma":0.0053450633,"teacher_disagreement_score":0.022933085,"about_ca_system_score_codex":0.003346124,"about_ca_system_score_gemma":0.004748173,"threshold_uncertainty_score":0.07678127},"labels":[],"label_agreement":null},{"id":"W2992954031","doi":"","title":"INFRA-RED IMAGING OF MEIBOMIAN GLANDS & EVALUATION OF THE LIPID LAYER IN SJOGREN’S SYNDROME PATIENTS","year":2013,"lang":"en","type":"article","venue":"Investigative Ophthalmology & Visual Science","topic":"Hereditary Neurological Disorders","field":"Neuroscience","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":"University of Waterloo","funders":"","keywords":"Meibomian gland; Medicine; Ophthalmology; Dermatology; Eyelid","score_opus":0.060428667193205485,"score_gpt":0.33291627449372724,"score_spread":0.27248760730052174,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2992954031","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":[0.9926443,0.001406044,0.00029819438,0.0002741411,0.00001614539,0.000012644268,0.00007117012,0.000022516697,0.0052548572],"genre_scores_gemma":[0.99853945,0.00047928785,0.00035929558,0.000098804914,0.000023709425,0.0000036783333,0.000040477742,0.000007289521,0.00044810018],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9998424,0.000021225553,0.000028052915,0.00002219651,0.00003594441,0.000050196842],"domain_scores_gemma":[0.9997609,0.00008154473,0.00003624901,0.000016097494,0.000032747408,0.000072396084],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00041356814,0.000687323,0.00022975894,0.0018984184,0.00037397386,0.00040306943,0.00033219485,0.00076446676,0.0024073985],"category_scores_gemma":[0.0010162934,0.000363413,0.00037501723,0.00042565525,0.00041701036,0.00077313144,0.00028337174,0.0004343033,0.00032760523],"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":[0.0022381307,0.00022194059,0.57748586,0.00012635987,0.00013163002,0.31530994,0.000697931,0.00065994135,0.08069457,0.00045750657,0.0009864958,0.020989742],"study_design_scores_gemma":[0.00009652165,0.00064798514,0.60222495,0.00007001323,0.00021028334,0.37037617,0.00097441545,0.0020524226,0.020989563,0.00064557773,0.0016737826,0.00003828025],"about_ca_topic_score_codex":0.0021272453,"about_ca_topic_score_gemma":0.0015354011,"teacher_disagreement_score":0.0024073985,"about_ca_system_score_codex":0.00028375266,"about_ca_system_score_gemma":0.0002462117,"threshold_uncertainty_score":0.008053541},"labels":[],"label_agreement":null},{"id":"W2992983681","doi":"10.1111/nmo.13773","title":"Characterization of gastrointestinal pathologies in the <i>dystonia musculorum</i> mouse model for hereditary sensory and autonomic neuropathy type VI","year":2019,"lang":"en","type":"article","venue":"Neurogastroenterology & Motility","topic":"Hereditary Neurological Disorders","field":"Neuroscience","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":"Ottawa Hospital; University of Ottawa","funders":"Canadian Institutes of Health Research; Genome Canada","keywords":"Neurodegeneration; Enteric nervous system; Pathology; Medicine; Ataxia; Internal medicine; Endocrinology; Biology; Neuroscience; Disease","score_opus":0.029054046664478108,"score_gpt":0.2448579795489332,"score_spread":0.2158039328844551,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2992983681","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":[0.9813255,0.0012259042,0.0066989986,0.0005161219,0.00013393622,0.00035192666,0.0054181404,0.00051355775,0.0038158568],"genre_scores_gemma":[0.95330715,0.0016614104,0.015533757,0.0005077963,0.000042987762,0.0008785513,0.007082454,0.00030880223,0.020677175],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9994721,0.000055990593,0.00008323644,0.00017252403,0.00011719484,0.00009891786],"domain_scores_gemma":[0.99940705,0.00004111246,0.00020790113,0.000046965473,0.00005313512,0.00024388975],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0004286436,0.0012181329,0.0005231909,0.00149755,0.0005637073,0.000625274,0.0005271329,0.0011890879,0.003237194],"category_scores_gemma":[0.00017582485,0.00047375335,0.0008775795,0.00037647007,0.0007091772,0.0004852467,0.00048723855,0.0016797355,0.0010046522],"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":[0.00026128013,0.00015827322,0.00057798944,0.000065605775,0.000017177816,0.00022521263,0.000041967873,0.00007918194,0.9973596,0.00025468413,0.00017146334,0.0007876008],"study_design_scores_gemma":[0.0002793873,0.0031001542,0.04161043,0.00013195458,0.00017311508,0.003802921,0.00040213877,0.00323472,0.9363554,0.00037939605,0.010475731,0.000054481752],"about_ca_topic_score_codex":0.0011511868,"about_ca_topic_score_gemma":0.0023389126,"teacher_disagreement_score":0.003237194,"about_ca_system_score_codex":0.00070340984,"about_ca_system_score_gemma":0.000377499,"threshold_uncertainty_score":0.010829449},"labels":[],"label_agreement":null},{"id":"W2994831994","doi":"10.2174/1381612825666191210154535","title":"Neurofilament Proteins as Prognostic Biomarkers in Neurological Disorders","year":2019,"lang":"en","type":"review","venue":"Current Pharmaceutical Design","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":81,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of British Columbia","funders":"","keywords":"Neurofilament; Medicine; Neuroscience; Pathology; Bioinformatics; Biology; Immunohistochemistry","score_opus":0.33932696658424005,"score_gpt":0.4450565157748995,"score_spread":0.10572954919065947,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W2994831994","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":[0.0018112886,0.9949685,0.0007268501,0.0006573752,0.00046462737,0.000012202079,0.00013262745,0.000027859278,0.0011987727],"genre_scores_gemma":[0.026253812,0.96702343,0.0023243974,0.0007572867,0.0014007053,0.000060307815,0.00060132,0.000009843441,0.0015688667],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.9995956,0.00010491586,0.00006807877,0.00007363487,0.00012559071,0.000032210068],"domain_scores_gemma":[0.9995734,0.000178907,0.00007868286,0.000009193403,0.00012910052,0.00003075168],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0012312217,0.0006791811,0.0009516752,0.0016477926,0.00016894101,0.0009062099,0.000486241,0.0006792584,0.0014212535],"category_scores_gemma":[0.0014233096,0.0001110504,0.00042155822,0.0014732365,0.0002845128,0.00060852,0.00040945035,0.000812355,0.0008730852],"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":[0.00029346783,0.00006762091,0.009854331,0.00581196,0.00031184658,0.00043927954,0.00013366359,0.00026738495,0.0032872856,0.0020009743,0.022407087,0.95512515],"study_design_scores_gemma":[0.00010065252,0.0009047944,0.06539445,0.011510906,0.001664546,0.0091657275,0.0004061245,0.001083711,0.006606363,0.007743675,0.89526147,0.00015749363],"about_ca_topic_score_codex":0.00061618706,"about_ca_topic_score_gemma":0.0007049033,"teacher_disagreement_score":0.0016477926,"about_ca_system_score_codex":0.00041433214,"about_ca_system_score_gemma":0.0005423354,"threshold_uncertainty_score":0.00651139},"labels":[],"label_agreement":null},{"id":"W3000368710","doi":"10.1002/mgg3.1052","title":"Clinical and genetic analysis of <i>ATP13A2</i> in hereditary spastic paraplegia expands the phenotype","year":2020,"lang":"en","type":"article","venue":"Molecular Genetics & Genomic Medicine","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":28,"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; Université Laval; Montreal Neurological Institute and Hospital","funders":"Canadian Institutes of Health Research","keywords":"Hereditary spastic paraplegia; Spasticity; Medicine; Exome sequencing; Spastic; Phenotype; Mutation; Extrapyramidal symptoms; Paraplegia; Genetics; Bioinformatics; Psychiatry; Gene; Biology; Physical medicine and rehabilitation; Spinal cord; Schizophrenia (object-oriented programming)","score_opus":0.045582376969524906,"score_gpt":0.2969445689081327,"score_spread":0.2513621919386078,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W3000368710","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":[0.99160963,0.00047604696,0.0007155099,0.00016610467,0.000017738743,0.000059702175,0.00067574024,0.00004682227,0.006232806],"genre_scores_gemma":[0.9978835,0.00020617688,0.00058851234,0.00016046572,0.000022043181,0.0000095330215,0.0005632121,0.00001793011,0.00054857315],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9997944,0.000024008703,0.000024112695,0.000059083068,0.00005274055,0.00004560181],"domain_scores_gemma":[0.9996486,0.00008402395,0.000072208815,0.000016323074,0.000084994375,0.000093851864],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00023428835,0.0010368184,0.00029402666,0.00085387885,0.0005639978,0.0003322395,0.00032107913,0.00054662727,0.0040315567],"category_scores_gemma":[0.0007761269,0.00012247483,0.00028557755,0.0006828776,0.00045684076,0.00011390495,0.00036265614,0.00029653555,0.00056743494],"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":[0.0012849902,0.00033377728,0.52902913,0.0003004977,0.00024089144,0.25806057,0.0008658643,0.00073664926,0.16803853,0.0005363276,0.0040669185,0.03650575],"study_design_scores_gemma":[0.000078012374,0.00030708243,0.7821143,0.00011224164,0.00027138853,0.19847426,0.00033538468,0.001067906,0.011625429,0.0002867003,0.0053015742,0.000025635429],"about_ca_topic_score_codex":0.017338986,"about_ca_topic_score_gemma":0.022804426,"teacher_disagreement_score":0.017338986,"about_ca_system_score_codex":0.00045609582,"about_ca_system_score_gemma":0.0007188322,"threshold_uncertainty_score":0.03447616},"labels":[],"label_agreement":null},{"id":"W3004976779","doi":"10.1016/j.nmd.2020.02.002","title":"Phenotypic convergence in Charcot-Marie-Tooth 2Y with novel VCP mutation","year":2020,"lang":"en","type":"article","venue":"Neuromuscular Disorders","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":16,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"McMaster Children's Hospital; McMaster University","funders":"McMaster University","keywords":"Tooth disease; Proband; Phenotype; Genetics; Biology; Genetic heterogeneity; Mutation; Gene; Inheritance (genetic algorithm)","score_opus":0.028149716963550137,"score_gpt":0.22739901598279808,"score_spread":0.19924929901924793,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W3004976779","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":[0.9867632,0.0006287444,0.001938981,0.00065283437,0.00020525641,0.000051802104,0.00050047383,0.00015762729,0.0091011],"genre_scores_gemma":[0.99690175,0.00015332579,0.0012309909,0.000121504636,0.00010858894,0.00002146317,0.0001565334,0.00004400997,0.001261679],"study_design_codex":"case_report","study_design_gemma":"case_report","domain_scores_codex":[0.99926454,0.000069054295,0.00009723925,0.00023650656,0.00017452527,0.0001581611],"domain_scores_gemma":[0.99912006,0.0003282552,0.00016108678,0.000048246457,0.00009691784,0.00024544512],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0003376205,0.0017777678,0.0008098435,0.0025560218,0.001255106,0.0009079415,0.0011876656,0.0027058355,0.0068739005],"category_scores_gemma":[0.002046904,0.00038276377,0.0007301512,0.0010251567,0.0015781852,0.00061841245,0.0018135873,0.0009238982,0.00097225764],"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":[0.00024366395,0.00005016359,0.006313635,0.00006966205,0.00003854916,0.9419751,0.00031726292,0.00032711364,0.046342876,0.0008763508,0.000575268,0.002870264],"study_design_scores_gemma":[0.000053937543,0.000096651806,0.022047155,0.000025101377,0.00006735271,0.9635052,0.00021876874,0.0016311923,0.010207736,0.000697463,0.0014083445,0.000041101663],"about_ca_topic_score_codex":0.0026171308,"about_ca_topic_score_gemma":0.0019708036,"teacher_disagreement_score":0.0068739005,"about_ca_system_score_codex":0.0005919492,"about_ca_system_score_gemma":0.0005494889,"threshold_uncertainty_score":0.022995532},"labels":[],"label_agreement":null},{"id":"W3006717921","doi":"10.3389/fgene.2020.00061","title":"A Rare KIF1A Missense Mutation Enhances Synaptic Function and Increases Seizure Activity","year":2020,"lang":"en","type":"article","venue":"Frontiers in Genetics","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":35,"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":"Chongqing Medical University; Institute of Genetics; National Natural Science Foundation of China","keywords":"Missense mutation; Epilepsy; Zebrafish; Mutation; Exome sequencing; Neuroscience; Epileptogenesis; Hereditary spastic paraplegia; Biology; Epilepsy syndromes; Phenotype; Genetics; Gene","score_opus":0.023546453799180744,"score_gpt":0.23058165075105114,"score_spread":0.2070351969518704,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W3006717921","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":[0.9957281,0.00062072783,0.0014600708,0.00011945225,0.000036560843,0.000014432023,0.00047799016,0.00014627085,0.0013964125],"genre_scores_gemma":[0.99792105,0.0003060871,0.0007979138,0.000049462986,0.000010573806,0.000010431838,0.00022397787,0.000022661921,0.0006578255],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9999088,0.000009278558,0.000013265973,0.000028452558,0.000027420314,0.000012832121],"domain_scores_gemma":[0.999889,0.00003632727,0.000027452845,0.000009299066,0.00000932708,0.000028684857],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.000065782355,0.0006530066,0.0003128442,0.0003740628,0.00019151674,0.00010806008,0.0001856717,0.000470986,0.0022666112],"category_scores_gemma":[0.0003398826,0.000096381315,0.0002815824,0.00023295164,0.0002357037,0.00011089094,0.00025915354,0.0003187593,0.00042590714],"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":[0.00015112633,0.00007593647,0.007448701,0.000072032875,0.000067242945,0.01748533,0.000062459345,0.00021892249,0.96399665,0.00025257465,0.00043896964,0.009730116],"study_design_scores_gemma":[0.00010463492,0.0009276937,0.2634673,0.00006980958,0.00026887443,0.22510256,0.00027270074,0.004779716,0.49348474,0.0013573004,0.010094183,0.00007044002],"about_ca_topic_score_codex":0.0010462048,"about_ca_topic_score_gemma":0.0018391843,"teacher_disagreement_score":0.0022666112,"about_ca_system_score_codex":0.00017705518,"about_ca_system_score_gemma":0.00013881642,"threshold_uncertainty_score":0.007582605},"labels":[],"label_agreement":null},{"id":"W3009065377","doi":"10.1159/000506193","title":"Myofibrillar Myopathy Mimicking Polyneuropathy","year":2020,"lang":"en","type":"article","venue":"Case Reports in Neurology","topic":"Hereditary Neurological Disorders","field":"Neuroscience","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":"Children's Hospital of Eastern Ontario; Ottawa Hospital","funders":"","keywords":"Medicine; Myopathy; Polyneuropathy; Myofibril; Physical medicine and rehabilitation; Internal medicine","score_opus":0.05058118124101132,"score_gpt":0.2587901216023814,"score_spread":0.20820894036137008,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W3009065377","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":[0.9740408,0.0022901988,0.0010790158,0.0008151631,0.00018359082,0.00016420618,0.0003521778,0.00017979997,0.02089498],"genre_scores_gemma":[0.99514174,0.0008904883,0.00042589387,0.0004922403,0.0001825938,0.000016082397,0.00012859188,0.000012233441,0.0027101866],"study_design_codex":"case_report","study_design_gemma":"case_report","domain_scores_codex":[0.99984014,0.000012271827,0.000013820105,0.00004960946,0.00002144789,0.00006267905],"domain_scores_gemma":[0.9997191,0.0000724814,0.000054311855,0.000022602944,0.000022850132,0.00010863588],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00015328401,0.0011708584,0.0004970817,0.0008865884,0.0010015119,0.00046403875,0.00047205103,0.0013951375,0.003659457],"category_scores_gemma":[0.0008819695,0.00032581613,0.0003510843,0.00065469416,0.0005159009,0.0006647697,0.0005618939,0.0009148573,0.0011807143],"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":[0.00006275858,0.0000468817,0.01066012,0.00005769364,0.000009951332,0.98424584,0.0001630979,0.00010226115,0.0027064395,0.00018684861,0.00034330686,0.0014148336],"study_design_scores_gemma":[0.000029464198,0.00027904508,0.034605693,0.000027273742,0.000022445854,0.9622285,0.000118472526,0.00036371598,0.00081710576,0.00031703926,0.0011798005,0.000011363642],"about_ca_topic_score_codex":0.001856102,"about_ca_topic_score_gemma":0.0026881618,"teacher_disagreement_score":0.003659457,"about_ca_system_score_codex":0.00041790612,"about_ca_system_score_gemma":0.0002983095,"threshold_uncertainty_score":0.012242079},"labels":[],"label_agreement":null},{"id":"W3010367570","doi":"10.1038/s10038-020-0734-x","title":"A novel biallelic single base insertion in WNK1 in a Pakistani family with congenital insensitivity to pain","year":2020,"lang":"en","type":"article","venue":"Journal of Human Genetics","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":3,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Toronto; Centre for Addiction and Mental Health","funders":"Canadian Institutes of Health Research; Government of Canada","keywords":"Genetics; Exome sequencing; Disease gene identification; Nonsense; Biology; Consanguinity; Exon; Nonsense mutation; Gene; Mutation; Missense mutation","score_opus":0.09235442113680066,"score_gpt":0.27236995871172437,"score_spread":0.18001553757492372,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W3010367570","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":[0.990728,0.00047137274,0.0022013446,0.0010054416,0.00024734478,0.00006727789,0.00044920534,0.00009127953,0.004738639],"genre_scores_gemma":[0.9970477,0.00016137195,0.0010682975,0.00023662076,0.0000808238,0.000012050333,0.00009455543,0.00002521734,0.0012732691],"study_design_codex":"case_report","study_design_gemma":"observational","domain_scores_codex":[0.99962807,0.0000374301,0.0000558386,0.00013300568,0.00006795223,0.000077712975],"domain_scores_gemma":[0.9989536,0.0004051039,0.00030624695,0.000050631927,0.000053803476,0.00023057438],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0001688328,0.001901271,0.0005341058,0.0015989207,0.0018182955,0.00057899085,0.0013583422,0.0022562086,0.005505273],"category_scores_gemma":[0.0016582981,0.00046142552,0.0008439787,0.0011923221,0.00148096,0.00049383723,0.0008833105,0.0015344255,0.0007830701],"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":[0.00016809387,0.000073152456,0.009193769,0.00004678771,0.000040304956,0.9621132,0.0004733582,0.00018313255,0.024276532,0.00037018248,0.00032422287,0.0027372406],"study_design_scores_gemma":[0.000060954688,0.0002076716,0.02878519,0.000042302847,0.00014887664,0.9609533,0.00048297807,0.0007089466,0.0065930183,0.0003198705,0.0016422725,0.00005460541],"about_ca_topic_score_codex":0.004160428,"about_ca_topic_score_gemma":0.004415344,"teacher_disagreement_score":0.005505273,"about_ca_system_score_codex":0.00054526184,"about_ca_system_score_gemma":0.00067685643,"threshold_uncertainty_score":0.018416941},"labels":[],"label_agreement":null},{"id":"W3016056304","doi":"10.1172/jci136162","title":"(H)Elping nerve growth factor: Elp1 inhibits TrkA’s phosphatase to maintain retrograde signaling","year":2020,"lang":"en","type":"letter","venue":"Journal of Clinical Investigation","topic":"Hereditary Neurological Disorders","field":"Neuroscience","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":"Hospital for Sick Children; University of Toronto","funders":"","keywords":"Nerve growth factor; Tropomyosin receptor kinase A; Cell biology; Neuroscience; Neurotrophin; Biology; Low-affinity nerve growth factor receptor; Signal transduction; Receptor; Genetics","score_opus":0.17430240895444746,"score_gpt":0.36131712887805945,"score_spread":0.187014719923612,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W3016056304","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":[0.036122102,0.00801845,0.0026590568,0.8399931,0.07195149,0.00020408686,0.00026019572,0.0007140621,0.04007738],"genre_scores_gemma":[0.17807955,0.009265607,0.002997744,0.6063458,0.15409799,0.00022489791,0.00021142582,0.00014796304,0.048629053],"study_design_codex":"not_applicable","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99973494,0.000052155872,0.000035490197,0.00004148924,0.00007290635,0.000062929634],"domain_scores_gemma":[0.99941957,0.0002732658,0.00005341508,0.000039214043,0.00010021404,0.000114450864],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00045249998,0.0007255154,0.00053605053,0.00033757434,0.0009806597,0.0008231853,0.00065913354,0.008908315,0.0034533562],"category_scores_gemma":[0.002524249,0.00027862404,0.00063031435,0.00019689175,0.0011578954,0.0009822788,0.0002972327,0.0065666065,0.0041972324],"study_design_candidate":"bench_or_experimental","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.001196914,0.0003513882,0.0051037776,0.00032031888,0.00010195379,0.077003695,0.00025563463,0.0005260022,0.0146256145,0.0073065576,0.83827335,0.054934815],"study_design_scores_gemma":[0.0013301246,0.0011294221,0.011247468,0.00024450495,0.00019434548,0.1227387,0.0005367285,0.0057400777,0.02602583,0.015513198,0.81513596,0.00016365983],"about_ca_topic_score_codex":0.0016318797,"about_ca_topic_score_gemma":0.002194853,"teacher_disagreement_score":0.008908315,"about_ca_system_score_codex":0.0012935719,"about_ca_system_score_gemma":0.00041593603,"threshold_uncertainty_score":0.011552572},"labels":[],"label_agreement":null},{"id":"W3019628269","doi":"10.1111/jns.12379","title":"High glucose level as a modifier factor in <scp>CMT1A</scp> patients","year":2020,"lang":"en","type":"article","venue":"Journal of the Peripheral Nervous System","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":4,"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":"Fundação de Apoio ao Ensino, Pesquisa e Assistência do Hospital das Clínicas da Faculdade de Medicina de Ribeirão Preto da Universidade de São Paulo; Coordenação de Aperfeiçoamento de Pessoal de Nível Superior; Instituto Nacional de Ciência e Tecnologia Translacional em Medicina; Fundação de Amparo à Pesquisa do Estado de São Paulo","keywords":"Factor (programming language); Food science; Chemistry; Psychology; Medicine; Computer science","score_opus":0.04733462754544707,"score_gpt":0.23763085579040008,"score_spread":0.19029622824495301,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W3019628269","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":[0.9988405,0.0003308126,0.00007070097,0.000047689395,0.000011305629,0.000007377039,0.0001297939,0.0000050195517,0.00055679394],"genre_scores_gemma":[0.9996039,0.00008685055,0.000052529937,0.000022047221,0.00002059799,0.0000038546737,0.00012948397,0.0000020346572,0.00007880609],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9996401,0.00006403664,0.00004545818,0.0001041513,0.00007696353,0.00006926515],"domain_scores_gemma":[0.999065,0.00020144897,0.00045416495,0.00004774986,0.000046409055,0.00018524133],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0002695118,0.00040635746,0.00035496033,0.0009887674,0.0006588685,0.0006441947,0.0002939835,0.0005236414,0.0024885659],"category_scores_gemma":[0.0015828474,0.000199189,0.00046068427,0.0014409758,0.00028471442,0.00030975233,0.00039053572,0.00061083946,0.0002471473],"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":[0.00033753287,0.000028994604,0.99472755,0.000011413978,0.000033787164,0.00228005,0.000051969866,0.000039721777,0.0006082004,0.000027295222,0.00009896235,0.0017545553],"study_design_scores_gemma":[0.0000074712593,0.00015757527,0.99367464,0.000008871418,0.000039947867,0.0054812473,0.000100696314,0.00018497251,0.00012137886,0.000046313435,0.00017082135,0.0000061037754],"about_ca_topic_score_codex":0.0024623792,"about_ca_topic_score_gemma":0.0018012834,"teacher_disagreement_score":0.0024885659,"about_ca_system_score_codex":0.00024971226,"about_ca_system_score_gemma":0.00025847348,"threshold_uncertainty_score":0.00832504},"labels":[],"label_agreement":null},{"id":"W3020884142","doi":"10.1136/jmedgenet-2019-106641","title":"Comprehensive genetic sequence and copy number analysis for Charcot-Marie-Tooth disease in a Canadian cohort of 2517 patients","year":2020,"lang":"en","type":"article","venue":"Journal of Medical Genetics","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":34,"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; McMaster University; London Health Sciences Centre","funders":"","keywords":"Copy-number variation; Genetics; Mendelian inheritance; Gene duplication; Biology; Gene; Genetic testing; Exome sequencing; Sequence (biology); Genetic heterogeneity; OMIM : Online Mendelian Inheritance in Man; Bioinformatics; Mutation; Phenotype; Genome","score_opus":0.04876581059408354,"score_gpt":0.3036833615817918,"score_spread":0.2549175509877083,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W3020884142","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":[0.99486285,0.0003290841,0.00025176135,0.00010833337,0.000008978646,0.00005216912,0.0023022697,0.00001518156,0.0020693913],"genre_scores_gemma":[0.9965323,0.00037136418,0.00050861563,0.00008786233,0.0000067894784,0.000020675236,0.0015673519,0.000013905792,0.00089114736],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99915206,0.00003134005,0.000034887682,0.00023776553,0.00036411808,0.00017982555],"domain_scores_gemma":[0.9991172,0.000083539875,0.00011173318,0.000056880865,0.00041127103,0.00021940102],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00044751738,0.0007416161,0.00045208566,0.0019162612,0.0032954987,0.00083441735,0.00086584943,0.00044039884,0.002335889],"category_scores_gemma":[0.001670096,0.00035604328,0.00041864897,0.0022567853,0.0007704121,0.00020264409,0.00072169,0.00053855893,0.00030980224],"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":[0.00024993214,0.00006406813,0.9677315,0.000044633794,0.00011052302,0.0045982976,0.0019979351,0.0003581996,0.008233895,0.00034689202,0.0023389494,0.013925128],"study_design_scores_gemma":[0.000016319724,0.00006845914,0.99021775,0.0000214715,0.00007332025,0.005204485,0.00070949737,0.00046230928,0.00056083937,0.000054865748,0.0025748203,0.000035780868],"about_ca_topic_score_codex":0.9132951,"about_ca_topic_score_gemma":0.9182258,"teacher_disagreement_score":0.08670491,"about_ca_system_score_codex":0.0059872335,"about_ca_system_score_gemma":0.008480622,"threshold_uncertainty_score":0.17443103},"labels":[],"label_agreement":null},{"id":"W3022069984","doi":"10.1111/cge.13771","title":"Clinical and radiological characterization of novel <scp> <i>FIG4</i> </scp> ‐related combined system disease with neuropathy","year":2020,"lang":"en","type":"article","venue":"Clinical Genetics","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":17,"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":"H2020 European Research Council; Medical Research Council; Newton Fund; Medical Research Council Canada; Wellcome Trust","keywords":"Missense mutation; Hypotonia; Compound heterozygosity; Pathology; Medicine; Atrophy; Phenotype; Biology; Neuroscience; Internal medicine; Genetics; Gene","score_opus":0.08569528878985434,"score_gpt":0.29860115024296385,"score_spread":0.21290586145310952,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W3022069984","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":[0.9973248,0.00018173954,0.0004047822,0.0000929116,0.000008472918,0.000031198095,0.00014540035,0.000024923535,0.0017857554],"genre_scores_gemma":[0.99873596,0.00007766073,0.0005882769,0.00006388471,0.000020887812,0.000011988664,0.00013139205,0.000010971115,0.0003589768],"study_design_codex":"case_report","study_design_gemma":"observational","domain_scores_codex":[0.9996412,0.000041644616,0.000043204138,0.0001156667,0.00006722136,0.00009107548],"domain_scores_gemma":[0.99924964,0.00017628662,0.00017894802,0.000034186778,0.00006537732,0.0002954955],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00026429302,0.001384595,0.0005689407,0.0008713997,0.0006145911,0.00047975752,0.0005434979,0.0013304993,0.0020690854],"category_scores_gemma":[0.0012208231,0.00039379738,0.0003133379,0.0005464309,0.0012409597,0.00030957017,0.0005897054,0.0005715161,0.00036548165],"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":[0.0004400271,0.00017221607,0.13694213,0.00010074747,0.00006784694,0.79383326,0.0005481179,0.00039415836,0.062347118,0.0003214264,0.00067674235,0.004156299],"study_design_scores_gemma":[0.00006552743,0.00051988615,0.15315086,0.000019378018,0.00005783712,0.8413151,0.00013319479,0.00060087116,0.0033464239,0.00011139757,0.0006535231,0.000026073187],"about_ca_topic_score_codex":0.0038902154,"about_ca_topic_score_gemma":0.0033986727,"teacher_disagreement_score":0.0038902154,"about_ca_system_score_codex":0.0005423486,"about_ca_system_score_gemma":0.00046369672,"threshold_uncertainty_score":0.007735133},"labels":[],"label_agreement":null},{"id":"W3027783203","doi":"10.1097/00007632-200305010-00028","title":"Letters","year":2003,"lang":"sl","type":"letter","venue":"Spine","topic":"Hereditary Neurological Disorders","field":"Neuroscience","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":"Object Research Systems (Canada)","funders":"","keywords":"Medicine; Subject (documents); Library science","score_opus":0.03132144964246634,"score_gpt":0.2504377269519321,"score_spread":0.21911627730946578,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W3027783203","genre_codex":"commentary","genre_gemma":"editorial","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"editorial","genre_consensus":null,"domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.0061180983,0.0054488014,0.00027224148,0.8390698,0.044654697,0.000055871064,0.00035054315,0.00016975038,0.103860185],"genre_scores_gemma":[0.1144051,0.009293661,0.00062117394,0.5812659,0.0777909,0.00014733829,0.00072073855,0.00014108047,0.21561407],"study_design_codex":"not_applicable","study_design_gemma":"not_applicable","domain_scores_codex":[0.9995598,0.00011560733,0.000043766377,0.0000786026,0.00010658964,0.00009559638],"domain_scores_gemma":[0.99882764,0.00038571612,0.00006838736,0.00006580675,0.00036227162,0.00029014348],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0004084054,0.00050611945,0.00063858373,0.0004942632,0.0013724784,0.0014449258,0.0008821452,0.009507488,0.056182392],"category_scores_gemma":[0.005388489,0.0002099898,0.0004972822,0.00033521172,0.00063040596,0.0010755064,0.0003632857,0.00563281,0.023284398],"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":[0.00016098647,0.000058283254,0.0017853915,0.000053958127,0.000019714837,0.0362925,0.00009880251,0.00007245062,0.00023917884,0.003007586,0.94355303,0.014658154],"study_design_scores_gemma":[0.00029848982,0.00008645193,0.0046192515,0.00028569723,0.000028936242,0.0770005,0.00043151644,0.00042010978,0.00038911778,0.009447235,0.9069614,0.0000314369],"about_ca_topic_score_codex":0.001761417,"about_ca_topic_score_gemma":0.0027835802,"teacher_disagreement_score":0.056182392,"about_ca_system_score_codex":0.0016201417,"about_ca_system_score_gemma":0.0011443312,"threshold_uncertainty_score":0},"labels":[],"label_agreement":null},{"id":"W3029855207","doi":"10.3389/fneur.2020.00399","title":"Cortical Damage Associated With Cognitive and Motor Impairment in Hereditary Spastic Paraplegia: Evidence of a Novel SPAST Mutation","year":2020,"lang":"en","type":"article","venue":"Frontiers in Neurology","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":14,"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":"Natural Science Foundation of Fujian Province; National Natural Science Foundation of China","keywords":"Hereditary spastic paraplegia; Neuroscience; Physical medicine and rehabilitation; Paraplegia; Medicine; Cognition; Cognitive impairment; Spastic; Psychology; Cerebral palsy; Spinal cord; Phenotype; Genetics; Biology","score_opus":0.03803777678263875,"score_gpt":0.25891606464293654,"score_spread":0.22087828786029778,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W3029855207","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":[0.9997029,0.000048211383,0.000051692252,0.000009843647,9.990401e-7,0.0000049652035,0.000034487304,0.000004062751,0.0001429091],"genre_scores_gemma":[0.9997559,0.00003112258,0.0000681782,0.000010626072,0.000004078363,0.0000031221532,0.000058672926,0.0000012677822,0.00006707832],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9998739,0.000023442262,0.00001643304,0.000031309584,0.000029793362,0.000025151652],"domain_scores_gemma":[0.9996747,0.00006188419,0.0001260616,0.000018396466,0.000034832003,0.00008423396],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00018292162,0.0008167478,0.0003249008,0.001215972,0.00043727958,0.0002384353,0.00029663846,0.00039732805,0.0020222343],"category_scores_gemma":[0.0006704556,0.00023949407,0.00020644315,0.0005811869,0.0006297211,0.00012834197,0.0004059186,0.00020015636,0.00017002506],"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":[0.0012692031,0.0002441536,0.8278976,0.0001430716,0.0002961007,0.07225504,0.000687809,0.00054749596,0.0860362,0.00014302152,0.00029099124,0.010189443],"study_design_scores_gemma":[0.000042061838,0.00035622143,0.96356034,0.000012050666,0.00008116985,0.032981064,0.00010939443,0.0004811983,0.0020966716,0.00009019169,0.00017993641,0.00000982122],"about_ca_topic_score_codex":0.0046020234,"about_ca_topic_score_gemma":0.0038057687,"teacher_disagreement_score":0.0046020234,"about_ca_system_score_codex":0.00025046003,"about_ca_system_score_gemma":0.00031968602,"threshold_uncertainty_score":0.009150445},"labels":[],"label_agreement":null},{"id":"W3034820387","doi":"10.1111/febs.15449","title":"Neuropathy‐associated histidyl‐tRNA synthetase variants attenuate protein synthesis <i>in vitro</i> and disrupt axon outgrowth in developing zebrafish","year":2020,"lang":"en","type":"article","venue":"FEBS Journal","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":24,"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 Lethbridge","funders":"National Institute of General Medical Sciences; National Institutes of Health","keywords":"Zebrafish; In vitro; Axon; Aminoacyl tRNA synthetase; Transfer RNA; Axon guidance; Chemistry; Biology; Molecular biology; Cell biology; Genetics; RNA; Gene","score_opus":0.03972892141231931,"score_gpt":0.23596340845584102,"score_spread":0.1962344870435217,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W3034820387","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":[0.9962592,0.0005727626,0.0012011043,0.00008175784,0.000027003383,0.000035966124,0.00032413471,0.000080770515,0.0014173387],"genre_scores_gemma":[0.99257034,0.00069933,0.001939667,0.000058110953,0.0000048307043,0.00005430056,0.00041112158,0.00004998091,0.0042123264],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9998172,0.000024592116,0.000027945827,0.00003356859,0.000054488963,0.000042295527],"domain_scores_gemma":[0.99985266,0.00002245044,0.000053107437,0.0000115278,0.000011240716,0.00004891968],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00018710895,0.0005114877,0.00025980297,0.0002449931,0.00023021834,0.00026082277,0.00028852557,0.0002911407,0.0009654109],"category_scores_gemma":[0.00012902434,0.00024504896,0.0003636055,0.000109324326,0.0003266101,0.00016128569,0.00025061364,0.000583209,0.0003353845],"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":[0.000045322402,0.000015177615,0.000089538065,0.000016072332,0.0000037475518,0.000047087095,0.000013526518,0.000074152966,0.9993555,0.000047311936,0.000019372019,0.00027331605],"study_design_scores_gemma":[0.000018130737,0.0004405423,0.0029212872,0.000007951748,0.000014692355,0.0001196631,0.00003646478,0.0007370761,0.9943116,0.000024241555,0.0013620643,0.000006231805],"about_ca_topic_score_codex":0.0070125926,"about_ca_topic_score_gemma":0.014445924,"teacher_disagreement_score":0.0070125926,"about_ca_system_score_codex":0.0008999466,"about_ca_system_score_gemma":0.0005302037,"threshold_uncertainty_score":0.013943553},"labels":[],"label_agreement":null},{"id":"W3044396894","doi":"10.1093/omcr/omaa046","title":"Painless: a case of congenital insensitivity to pain in a 5-year-old male","year":2020,"lang":"en","type":"article","venue":"Oxford Medical Case Reports","topic":"Hereditary Neurological Disorders","field":"Neuroscience","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":"University of Alberta","funders":"","keywords":"Medicine; Pediatrics","score_opus":0.03705759206150429,"score_gpt":0.2762715505265247,"score_spread":0.23921395846502042,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W3044396894","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":[0.9883801,0.0022517145,0.0007976422,0.0019251137,0.0002706319,0.00007273178,0.00026336894,0.0001003066,0.005938429],"genre_scores_gemma":[0.9966485,0.0006809754,0.0005365223,0.0005322128,0.00018679547,0.00001293747,0.00008409589,0.000018273908,0.0012997139],"study_design_codex":"case_report","study_design_gemma":"case_report","domain_scores_codex":[0.99928766,0.000044738874,0.000063553234,0.00019716893,0.00012380585,0.00028312617],"domain_scores_gemma":[0.9987128,0.00027497552,0.00031911503,0.000055493398,0.000074199466,0.00056347885],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00031852478,0.0018288349,0.0012612958,0.0032977862,0.0026589937,0.0015994734,0.0017033492,0.004465231,0.0035662923],"category_scores_gemma":[0.00240487,0.0010903483,0.0010805138,0.0015889489,0.0018456216,0.0015732552,0.0019212188,0.0030374972,0.00076956785],"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":[0.0000081379485,0.000024142822,0.0026947795,0.000009753885,0.0000027717776,0.99640334,0.00012405524,0.000014381897,0.00030244552,0.000060737497,0.000064277374,0.0002911032],"study_design_scores_gemma":[0.0000029911614,0.000048302987,0.0060583996,0.0000080765985,0.000005236401,0.99343735,0.00011239975,0.00004981453,0.00010536889,0.00003604929,0.00013052521,0.0000055021856],"about_ca_topic_score_codex":0.0057486193,"about_ca_topic_score_gemma":0.0070704743,"teacher_disagreement_score":0.0057486193,"about_ca_system_score_codex":0.0015348361,"about_ca_system_score_gemma":0.0010625821,"threshold_uncertainty_score":0.011930466},"labels":[],"label_agreement":null},{"id":"W3046354882","doi":"10.1038/s41436-020-0924-0","title":"Assessing non-Mendelian inheritance in inherited axonopathies","year":2020,"lang":"en","type":"article","venue":"Genetics in Medicine","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":27,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Université Laval; University of Alberta; Hospital for Sick Children; McMaster University; Children's Hospital of Eastern Ontario; McGill University; University of Ottawa; SickKids Foundation; University of Toronto; Montreal Neurological Institute and Hospital","funders":"National Institute of Neurological Disorders and Stroke; Muscular Dystrophy Association; Canadian Institutes of Health Research; Charcot-Marie-Tooth Association","keywords":"Mendelian inheritance; Genetics; Allele; Exome sequencing; Penetrance; Exome; Biology; Odds ratio; Medicine; Disease; Genetic heterogeneity; Gene; Bioinformatics; Mutation; Phenotype; Internal medicine","score_opus":0.141098031692705,"score_gpt":0.3419803173440342,"score_spread":0.20088228565132923,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W3046354882","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":[0.9880768,0.00059250963,0.0064303866,0.00012916181,0.000027584165,0.000039888946,0.00052738166,0.00007128008,0.0041050264],"genre_scores_gemma":[0.99193794,0.00020154004,0.0069038593,0.00003914144,0.0000141703185,0.000021717451,0.00024852363,0.000039549606,0.00059352117],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9939236,0.0024895358,0.00088232046,0.00094531063,0.0014138394,0.0003452835],"domain_scores_gemma":[0.9753117,0.017420717,0.0030709887,0.0012822949,0.002175544,0.0007387994],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.008223686,0.0012529494,0.0006388961,0.004492776,0.0006373595,0.0012989319,0.0010137496,0.0009939257,0.0043791044],"category_scores_gemma":[0.027355548,0.00027434062,0.0005742775,0.001571137,0.00073890435,0.0012367123,0.0013494149,0.00071989273,0.00047383716],"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":[0.00062129897,0.000113593145,0.9643111,0.00011720625,0.00028102298,0.004398247,0.00043098384,0.0008391725,0.006663369,0.0008235208,0.0002875767,0.021112956],"study_design_scores_gemma":[0.000048543207,0.00052035454,0.9540899,0.00014124354,0.00045308712,0.02354731,0.00078879,0.0068121436,0.0066733393,0.00503123,0.0018518377,0.000042248575],"about_ca_topic_score_codex":0.003578219,"about_ca_topic_score_gemma":0.0060202223,"teacher_disagreement_score":0.008223686,"about_ca_system_score_codex":0.00044524498,"about_ca_system_score_gemma":0.0010967698,"threshold_uncertainty_score":0.043491483},"labels":[],"label_agreement":null},{"id":"W3046743004","doi":"10.1016/b978-0-12-821487-9.00001-5","title":"Elegant wiring: Structural beauty of the peripheral nervous system","year":2020,"lang":"en","type":"book-chapter","venue":"Elsevier eBooks","topic":"Hereditary Neurological Disorders","field":"Neuroscience","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":"University of Alberta","funders":"","keywords":"Neuroscience; Peripheral nervous system; Spinal cord; Sensory system; Anatomy; Schwann cell; Nervous system; Peripheral nerve; Biology; Sensation; Central nervous system","score_opus":0.02539321135899883,"score_gpt":0.2243149825614954,"score_spread":0.19892177120249657,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W3046743004","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":[0.0044496674,0.11741174,0.114226125,0.006190372,0.0041657807,0.000024390445,0.00019861873,0.0013277433,0.7520056],"genre_scores_gemma":[0.07861579,0.0999514,0.057517074,0.0025783,0.0035067855,0.0000953344,0.00025278126,0.00068681856,0.7567957],"study_design_codex":"theoretical_or_conceptual","study_design_gemma":"not_applicable","domain_scores_codex":[0.999918,0.000014143086,0.0000031176305,0.000020401269,0.000036446305,0.000007834037],"domain_scores_gemma":[0.9999074,0.000050746967,0.0000055736314,0.0000139467675,0.000012357212,0.000009983059],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00018886478,0.0007472297,0.0003130041,0.00058873923,0.0005219439,0.0021558027,0.00056345377,0.0008357617,0.01758922],"category_scores_gemma":[0.0003764173,0.000301601,0.0002607723,0.00045799714,0.002571576,0.0024552448,0.000876013,0.0020489828,0.005324861],"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":[0.000030791085,0.000012359551,0.000058974805,0.00019898648,0.00001275826,0.000122366,0.0002416593,0.0017898266,0.0063191256,0.7634457,0.06753376,0.16023377],"study_design_scores_gemma":[0.000005298341,0.000017843284,0.000116830495,0.000087059845,0.0000064158735,0.0004179554,0.00005333222,0.00082900276,0.0012489844,0.37501493,0.62218994,0.000012449018],"about_ca_topic_score_codex":0.00054864894,"about_ca_topic_score_gemma":0.0010923382,"teacher_disagreement_score":0.01758922,"about_ca_system_score_codex":0.00062986306,"about_ca_system_score_gemma":0.00038398686,"threshold_uncertainty_score":0.058841765},"labels":[],"label_agreement":null},{"id":"W3083270173","doi":"10.3389/fnins.2020.00912","title":"Suppression of spastin Mutant Phenotypes by Pak3 Loss Implicates a Role for Reactive Glia in AD-HSP","year":2020,"lang":"en","type":"article","venue":"Frontiers in Neuroscience","topic":"Hereditary Neurological Disorders","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":"Institute of Genetics; National Institutes of Health","keywords":"Mutant; Phenotype; Cell biology; Downregulation and upregulation; Neuroscience; Chemistry; Biology; Genetics; Gene","score_opus":0.02319946264578413,"score_gpt":0.25571902178272177,"score_spread":0.23251955913693764,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W3083270173","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":[0.99580365,0.00037468428,0.0021104545,0.000065632674,0.000008989075,0.000008128158,0.0003611965,0.0001279392,0.001139339],"genre_scores_gemma":[0.9958801,0.00022438305,0.0012568301,0.00002451844,0.000002189464,0.00001119834,0.00042195708,0.000026170204,0.0021526655],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99995244,0.000005211766,0.000006293999,0.000012443413,0.00001228235,0.000011368604],"domain_scores_gemma":[0.999931,0.0000044620133,0.00001947623,0.000010467394,0.000007037448,0.000027611488],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0000620101,0.00032020453,0.00015399438,0.00025404085,0.00021845462,0.00018311306,0.00012233734,0.00016147173,0.0017833302],"category_scores_gemma":[0.00006981256,0.00014188664,0.00027992047,0.00010192497,0.00024292807,0.0001823254,0.00018500458,0.00048221566,0.00048373282],"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":[0.000054876036,0.000014416969,0.00040588004,0.00002094594,0.000003901827,0.00013353069,0.000010373126,0.0000534286,0.99841785,0.00008914339,0.000030320229,0.00076536374],"study_design_scores_gemma":[0.000017119484,0.000210005,0.03338094,0.000012320452,0.000018963823,0.002792239,0.00004196004,0.0021155807,0.95854163,0.00021379457,0.0026496877,0.000005732384],"about_ca_topic_score_codex":0.00058267923,"about_ca_topic_score_gemma":0.0010796294,"teacher_disagreement_score":0.0017833302,"about_ca_system_score_codex":0.00021188881,"about_ca_system_score_gemma":0.00013608694,"threshold_uncertainty_score":0.0059658885},"labels":[],"label_agreement":null},{"id":"W3086204915","doi":"10.1111/ene.14514","title":"Inherited neuropathies with predominant upper limb involvement: genetic heterogeneity and overlapping pathologies","year":2020,"lang":"en","type":"article","venue":"European Journal of Neurology","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":6,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Ottawa Hospital; Children's Hospital of Eastern Ontario; University of Ottawa","funders":"Wellcome Trust Centre for Mitochondrial Research; Medical Research Council; Canada Foundation for Innovation; Evelyn Trust; Newton Fund; Canadian Institutes of Health Research; Ataxia UK; Wellcome Trust","keywords":"Medicine; Genetic heterogeneity; Myopathy; Phenotype; Genetic testing; Neuromuscular disease; Peripheral neuropathy; Disease; Spinal muscular atrophy; Bioinformatics; Genetics; Pathology; Gene; Internal medicine; Biology; Endocrinology","score_opus":0.04529815639172651,"score_gpt":0.22731222660884345,"score_spread":0.18201407021711694,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W3086204915","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":[0.9992884,0.00026926442,0.000096415104,0.000018187598,0.0000012959514,0.0000050520457,0.000046682162,0.0000035618432,0.00027129866],"genre_scores_gemma":[0.99934226,0.0002127305,0.00015966289,0.000024331626,0.000011876102,0.000005951144,0.00014124629,0.0000032895691,0.00009869235],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9995678,0.00007445227,0.00005714744,0.0001626767,0.00006999382,0.00006797406],"domain_scores_gemma":[0.999345,0.00019700076,0.0002880259,0.000042371412,0.000054022858,0.000073624054],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00028709788,0.00055904686,0.00059345836,0.0008301558,0.0004067464,0.00047904695,0.00029422238,0.0004042045,0.0023153883],"category_scores_gemma":[0.0010844184,0.00016219838,0.00023110132,0.0009305373,0.0005211189,0.00026839683,0.00053751224,0.0002220826,0.0002529976],"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":[0.00080838916,0.00016009549,0.8650717,0.00019239035,0.0003343592,0.078623526,0.00079666125,0.00046223536,0.033800177,0.00034508988,0.0003772511,0.01902821],"study_design_scores_gemma":[0.000049437684,0.00019699971,0.84550387,0.000050857307,0.000097922195,0.15170816,0.00042463074,0.00026030384,0.0009885953,0.00030427641,0.0004000473,0.000015009753],"about_ca_topic_score_codex":0.0007850227,"about_ca_topic_score_gemma":0.0010165751,"teacher_disagreement_score":0.0023153883,"about_ca_system_score_codex":0.00019581076,"about_ca_system_score_gemma":0.00021714861,"threshold_uncertainty_score":0.0077458024},"labels":[],"label_agreement":null},{"id":"W3087910839","doi":"10.1093/brain/awz307","title":"Defining the clinical, molecular and imaging spectrum of adaptor protein complex 4-associated hereditary spastic paraplegia","year":2019,"lang":"en","type":"article","venue":"Brain","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":75,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"SickKids Foundation; Hospital for Sick Children; University of Toronto","funders":"","keywords":"Hereditary spastic paraplegia; Ventriculomegaly; Hypotonia; Corpus callosum; Microcephaly; Pediatrics; Pseudobulbar palsy; Medicine; Spastic; Psychology; Audiology; Physical medicine and rehabilitation; Cerebral palsy; Neuroscience; Genetics; Biology; Phenotype","score_opus":0.031487657455397076,"score_gpt":0.2872958289075265,"score_spread":0.2558081714521294,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W3087910839","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":[0.9995221,0.000068272646,0.000084148916,0.000011554956,8.4347766e-7,0.0000050095246,0.000050418595,0.000002825031,0.00025481122],"genre_scores_gemma":[0.99954706,0.00004932502,0.00015528838,0.000022526907,0.000004467103,0.0000061564524,0.00015105955,0.0000021052335,0.00006204268],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99965775,0.00007735665,0.000064296146,0.000093281466,0.000053444113,0.00005390681],"domain_scores_gemma":[0.99951804,0.00013684672,0.00015369359,0.00002455397,0.00005368812,0.00011318106],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00031418682,0.0006286671,0.00034757255,0.0011220472,0.00038535835,0.00033813785,0.00028770615,0.0004395692,0.0013361737],"category_scores_gemma":[0.0014909038,0.00025328287,0.00017551983,0.0004898198,0.00039894602,0.00039186692,0.0006436927,0.0002354589,0.00025509566],"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":[0.00018648579,0.000048996415,0.9760527,0.000014388017,0.000030787665,0.0092581045,0.00025658967,0.00011182911,0.011238153,0.00005351745,0.00008418513,0.002664172],"study_design_scores_gemma":[0.000014879844,0.00020258105,0.95214623,0.000009496572,0.000028919394,0.046064004,0.00027435055,0.00022294844,0.00079403113,0.00005558715,0.00018046067,0.0000066178122],"about_ca_topic_score_codex":0.0008668573,"about_ca_topic_score_gemma":0.0010164304,"teacher_disagreement_score":0.0013361737,"about_ca_system_score_codex":0.00016379297,"about_ca_system_score_gemma":0.00018654228,"threshold_uncertainty_score":0.0044699907},"labels":[],"label_agreement":null},{"id":"W3088205339","doi":"10.1101/2020.09.25.20176032","title":"Evidence for non-Mendelian inheritance in spastic paraplegia 7","year":2020,"lang":"en","type":"preprint","venue":"medRxiv","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":5,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":true,"ca_institutions":"University of Ottawa; McMaster University; SickKids Foundation; Montreal Neurological Institute and Hospital; University of Toronto; Children's Hospital of Eastern Ontario; McGill University; Hospital for Sick Children; University of Alberta; Université Laval","funders":"Fonds de Recherche du Québec - Santé; Canadian Institutes of Health Research; Parkinson Canada","keywords":"Hereditary spastic paraplegia; Paraplegia; Medicine; Spastic; Exome sequencing; Mendelian inheritance; Genetics; Pediatrics; Physical therapy; Mutation; Biology; Gene; Spinal cord; Phenotype; Psychiatry","score_opus":0.20862060584035097,"score_gpt":0.34762557843840175,"score_spread":0.13900497259805078,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W3088205339","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":[0.9808641,0.0034931283,0.0043769497,0.001145641,0.00014929782,0.00010144484,0.001686931,0.00016480294,0.008017589],"genre_scores_gemma":[0.99692494,0.00078786,0.00085595564,0.00013239591,0.00006893362,0.000018505556,0.0005107256,0.000021354152,0.00067930116],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99661994,0.0007080122,0.00021924559,0.00089448225,0.0012257072,0.00033264566],"domain_scores_gemma":[0.9945655,0.002397921,0.001182026,0.0005349523,0.0009251313,0.00039440772],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0020454912,0.0010382418,0.00058758527,0.0029299716,0.0010462767,0.0008498807,0.0013101221,0.0009408968,0.0105564045],"category_scores_gemma":[0.0070170765,0.00032134217,0.0008124285,0.0023622336,0.0012627327,0.00025737158,0.0006970732,0.0005795656,0.00046600707],"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":[0.000997917,0.00013095162,0.9413438,0.00035349134,0.0014044632,0.018191835,0.0008091694,0.00033649142,0.010358806,0.0039416687,0.0032007755,0.01893061],"study_design_scores_gemma":[0.00022004831,0.00030227719,0.9459804,0.00023303459,0.00083411677,0.04142761,0.0005193745,0.0021109676,0.0016863567,0.002132803,0.0044996496,0.000053397802],"about_ca_topic_score_codex":0.034817155,"about_ca_topic_score_gemma":0.023867263,"teacher_disagreement_score":0.034817155,"about_ca_system_score_codex":0.0007802147,"about_ca_system_score_gemma":0.0015370555,"threshold_uncertainty_score":0.06922901},"labels":[],"label_agreement":null},{"id":"W3092392868","doi":"10.1053/j.jfas.2020.09.015","title":"Ankle Fracture in Hereditary Sensory Neuropathy Type 1","year":2020,"lang":"en","type":"article","venue":"The Journal of Foot & Ankle Surgery","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":1,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Memorial University of Newfoundland","funders":"","keywords":"Ankle; Sensory neuropathy; Medicine; Hereditary motor and sensory neuropathy; Physical medicine and rehabilitation; Sensory system; Neuroscience; Psychology; Internal medicine; Anatomy; Disease","score_opus":0.07045920628342656,"score_gpt":0.2614104220562865,"score_spread":0.19095121577285995,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W3092392868","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":[0.9884067,0.00083524914,0.0004381782,0.0006249111,0.000098851015,0.000022747878,0.00014862098,0.000023574892,0.00940108],"genre_scores_gemma":[0.9979639,0.00022352015,0.00020538806,0.00017298954,0.000118509546,0.0000053079375,0.00006887759,0.000005521408,0.0012360989],"study_design_codex":"case_report","study_design_gemma":"case_report","domain_scores_codex":[0.99978274,0.000019710216,0.000025761354,0.000034449626,0.00004630658,0.00009104469],"domain_scores_gemma":[0.99962187,0.00012507063,0.000096601194,0.00001474307,0.00004841781,0.00009327732],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00013749578,0.0005212163,0.0003763328,0.0012236679,0.0012067219,0.00046382178,0.00060258433,0.0015155257,0.0070420494],"category_scores_gemma":[0.0018082767,0.00021821375,0.000411201,0.0009378662,0.00069085613,0.00039189306,0.00052103924,0.0006266787,0.0004740929],"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":[0.0005544115,0.00013576394,0.14281052,0.000058700833,0.000043032705,0.84274536,0.0003288489,0.00020748313,0.0031589628,0.0005493209,0.0010476463,0.008360019],"study_design_scores_gemma":[0.000043730746,0.00020144305,0.13414854,0.000044638364,0.00007161859,0.86182976,0.00059842947,0.0005853015,0.0007872049,0.0009732854,0.00069787394,0.000018103732],"about_ca_topic_score_codex":0.011439528,"about_ca_topic_score_gemma":0.010780479,"teacher_disagreement_score":0.011439528,"about_ca_system_score_codex":0.0005423765,"about_ca_system_score_gemma":0.0005948146,"threshold_uncertainty_score":0.02355802},"labels":[],"label_agreement":null},{"id":"W3093981954","doi":"10.1016/s1474-4422(20)30312-4","title":"Monogenic variants in dystonia: an exome-wide sequencing study","year":2020,"lang":"en","type":"article","venue":"The Lancet Neurology","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":214,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Children's Hospital of Eastern Ontario; University of Ottawa; Hospital for Sick Children; University of Toronto; SickKids Foundation","funders":"National Eye Institute; National Human Genome Research Institute; National Heart, Lung, and Blood Institute; Else Kröner-Fresenius-Stiftung; Technische Universität München; Bundesministerium für Bildung und Forschung; Eesti Teadusagentuur; Deutsche Forschungsgemeinschaft; Ministerstvo Školství, Mládeže a Tělovýchovy; Simons Foundation Autism Research Initiative; Vedecká Grantová Agentúra MŠVVaŠ SR a SAV; Broad Institute; Univerzita Karlova v Praze","keywords":"Dystonia; Exome sequencing; Medical genetics; Context (archaeology); Movement disorders; Medicine; Exome; Etiology; Genetics; Biology; Mutation; Psychiatry; Pathology; Disease; Gene","score_opus":0.14992170643258612,"score_gpt":0.30427913402324797,"score_spread":0.15435742759066184,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W3093981954","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":[0.99335384,0.0015441343,0.0005855133,0.0003736353,0.00003474634,0.000027696913,0.002885628,0.00002305887,0.0011717142],"genre_scores_gemma":[0.99637884,0.0005640731,0.00059973734,0.000281136,0.000040188635,0.000016026308,0.0014897638,0.000015091204,0.00061517756],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99953437,0.00006509479,0.0000571645,0.00020270616,0.00008072381,0.000060016075],"domain_scores_gemma":[0.9995454,0.00021107445,0.00008935911,0.000035388304,0.000039260744,0.000079486286],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00046820086,0.0011580107,0.0007128722,0.0009907467,0.0008941989,0.00088095956,0.00062430784,0.0017642061,0.0029239072],"category_scores_gemma":[0.0011931378,0.00031690273,0.00075208175,0.001378537,0.0003718357,0.00031741802,0.00067077903,0.0006602527,0.00042397733],"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":[0.007109108,0.0006134454,0.67681605,0.0006186486,0.005002581,0.10247,0.0020912592,0.0028429532,0.13961305,0.0018702633,0.0084856115,0.052466974],"study_design_scores_gemma":[0.00030628408,0.00035137183,0.9638568,0.00015782731,0.0018692717,0.024482511,0.00038750534,0.0015548442,0.0024364975,0.0008938755,0.003639488,0.00006366124],"about_ca_topic_score_codex":0.005356953,"about_ca_topic_score_gemma":0.010320177,"teacher_disagreement_score":0.005356953,"about_ca_system_score_codex":0.0003825467,"about_ca_system_score_gemma":0.0002979954,"threshold_uncertainty_score":0.010651588},"labels":[],"label_agreement":null},{"id":"W3107552929","doi":"10.1111/ene.14649","title":"Novel variants broaden the phenotypic spectrum of <i>PLEKHG5</i>‐associated neuropathies","year":2020,"lang":"en","type":"article","venue":"European Journal of Neurology","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":11,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Ottawa Hospital; Children's Hospital of Eastern Ontario; University of Ottawa","funders":"Center for Molecular Medicine Cologne, University of Cologne; Medical Research Council; Koç Üniversitesi Translasyonel Tıp Araştırma Merkezi; Deutsche Forschungsgemeinschaft","keywords":"Spinal muscular atrophy; Medicine; Exome sequencing; Amyotrophic lateral sclerosis; Disease; Genetics; Missense mutation; Phenotype; Bioinformatics; Pathology; Gene; Biology","score_opus":0.05226140144697131,"score_gpt":0.22744121199309733,"score_spread":0.17517981054612602,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W3107552929","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":[0.99510163,0.0011744304,0.0010424223,0.000106386404,0.000013892105,0.00001542201,0.00025182153,0.00006855662,0.0022255538],"genre_scores_gemma":[0.99884284,0.00022607064,0.0005066145,0.00007082463,0.000017335462,0.0000038871567,0.00014912334,0.000011711128,0.00017158967],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99982774,0.000020821935,0.00003649223,0.000055601464,0.00002952076,0.000029742649],"domain_scores_gemma":[0.999688,0.00013083252,0.00009653722,0.00001724954,0.00002882708,0.00003855706],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00023705866,0.0007832093,0.00029299746,0.0009456218,0.00030728453,0.0003876152,0.0003113057,0.0005463741,0.0025468175],"category_scores_gemma":[0.0006599073,0.00014766814,0.00031839602,0.00046056006,0.00044617287,0.00026226134,0.00048138076,0.0002798855,0.0003732672],"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":[0.0011187523,0.00012062224,0.47740543,0.00050399173,0.00041171457,0.18871023,0.001259198,0.0010530795,0.2649734,0.0010369661,0.0018528491,0.061553776],"study_design_scores_gemma":[0.000047560265,0.00025939514,0.62286085,0.00013114602,0.00026235924,0.35832304,0.00040050852,0.00068603345,0.011937487,0.0005274931,0.0045310864,0.00003297745],"about_ca_topic_score_codex":0.0005088215,"about_ca_topic_score_gemma":0.0008030078,"teacher_disagreement_score":0.0025468175,"about_ca_system_score_codex":0.000137123,"about_ca_system_score_gemma":0.000091186535,"threshold_uncertainty_score":0.0085199475},"labels":[],"label_agreement":null},{"id":"W3109560213","doi":"10.1038/s41436-020-01027-3","title":"An autosomal dominant neurological disorder caused by de novo variants in FAR1 resulting in uncontrolled synthesis of ether lipids","year":2020,"lang":"en","type":"article","venue":"Genetics in Medicine","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":49,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Mount Sinai Hospital; McMaster University; McMaster Children's Hospital","funders":"Common Fund; National Institutes of Health; National Institute of Neurological Disorders and Stroke; National Human Genome Research Institute; Amsterdam University Medical Centers","keywords":"Plasmalogen; Hypotonia; Spastic; Retinitis pigmentosa; Medicine; Biology; Internal medicine; Endocrinology; Gene; Biochemistry; Cerebral palsy; Phospholipid","score_opus":0.0354410844500562,"score_gpt":0.29276058845937164,"score_spread":0.25731950400931547,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W3109560213","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":[0.9980101,0.0006263579,0.00061073253,0.00006430302,0.0000073735982,0.000008615736,0.000098027405,0.000021202219,0.0005533072],"genre_scores_gemma":[0.99837565,0.00026149442,0.00071568385,0.00007060117,0.000011826848,0.0000055273013,0.00013453355,0.000008225482,0.00041643315],"study_design_codex":"case_report","study_design_gemma":"observational","domain_scores_codex":[0.99985623,0.000015236223,0.000019668025,0.000058557893,0.000019418136,0.000030800653],"domain_scores_gemma":[0.99973494,0.00007305544,0.00010914156,0.000015027122,0.000019720293,0.00004810385],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00016163748,0.0010292046,0.0003714819,0.00049512426,0.0005087536,0.0002658242,0.00028777722,0.0005566796,0.0020261728],"category_scores_gemma":[0.0004761499,0.00016063402,0.00025245736,0.00032907363,0.00043982887,0.00020139341,0.00038450534,0.00032141447,0.00041614764],"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":[0.0015614033,0.00031971605,0.2899252,0.00048936624,0.00026769435,0.33825368,0.0020112768,0.0006387849,0.32418495,0.0011157559,0.0007657257,0.0404665],"study_design_scores_gemma":[0.00011017899,0.00094201963,0.23211089,0.00007118584,0.00027909505,0.7191666,0.0006672237,0.0005642251,0.04211518,0.00049519376,0.003435396,0.0000428069],"about_ca_topic_score_codex":0.0006854911,"about_ca_topic_score_gemma":0.0007991369,"teacher_disagreement_score":0.0020261728,"about_ca_system_score_codex":0.00025339666,"about_ca_system_score_gemma":0.00025720327,"threshold_uncertainty_score":0.00677824},"labels":[],"label_agreement":null},{"id":"W3110604463","doi":"10.1017/cjn.2020.261","title":"Fatal Familial Insomnia with Early Dysautonomia and Diabetes","year":2020,"lang":"fr","type":"article","venue":"Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":2,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":true,"route_about_ca":false,"ca_institutions":"Kingston Health Sciences Centre; Queen's University","funders":"","keywords":"Dysautonomia; Familial dysautonomia; Medicine; Fatal familial insomnia; Content (measure theory); Insomnia; Psychology; Psychiatry; Internal medicine; Mathematics","score_opus":0.03459444339985922,"score_gpt":0.23473966142331953,"score_spread":0.2001452180234603,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W3110604463","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":[0.97198945,0.0031930308,0.0013595809,0.0026164106,0.0008069517,0.00015563838,0.0008965963,0.00020355523,0.018778848],"genre_scores_gemma":[0.9957898,0.0005336245,0.00015116966,0.0007198464,0.0003911433,0.000011422223,0.00021524384,0.000018182645,0.0021695243],"study_design_codex":"case_report","study_design_gemma":"case_report","domain_scores_codex":[0.99949193,0.000051293828,0.000050761642,0.000113416354,0.000111160545,0.0001813794],"domain_scores_gemma":[0.99883574,0.00017662815,0.00018919063,0.0001443388,0.00011197848,0.0005422251],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00046196987,0.00091555924,0.0007108993,0.0013705831,0.0028595075,0.0007015771,0.00060453906,0.0020120821,0.0034431068],"category_scores_gemma":[0.0020179574,0.00061600795,0.0008549364,0.0008534994,0.001140646,0.00047285575,0.00085913506,0.0023370164,0.00086227414],"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":[0.0008072152,0.0001838384,0.12202541,0.000060741822,0.000096289215,0.8687202,0.0002172184,0.00015818824,0.0012313734,0.00058320013,0.0022804625,0.0036359034],"study_design_scores_gemma":[0.00015882842,0.0005348669,0.19232419,0.00006247209,0.00011032381,0.8026253,0.00027843783,0.00037443207,0.0007132333,0.0012165998,0.0015519452,0.00004933751],"about_ca_topic_score_codex":0.018753905,"about_ca_topic_score_gemma":0.01738784,"teacher_disagreement_score":0.018753905,"about_ca_system_score_codex":0.0016354214,"about_ca_system_score_gemma":0.0012667116,"threshold_uncertainty_score":0.0372895},"labels":[],"label_agreement":null},{"id":"W3110618962","doi":"10.3390/genes11121426","title":"A CNTNAP1 Missense Variant Is Associated with Canine Laryngeal Paralysis and Polyneuropathy","year":2020,"lang":"en","type":"article","venue":"Genes","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":16,"is_retracted":false,"has_abstract":true,"route_ca_aff":false,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":true,"ca_institutions":"","funders":"National Institutes of Health; University of Bern; University of Minnesota","keywords":"Missense mutation; Paralysis; Polyneuropathy; Medicine; Laryngeal paralysis; Vocal cord paralysis; Anatomy; Biology; Mutation; Pathology; Genetics; Surgery; Gene","score_opus":0.03999460345162142,"score_gpt":0.21986440523196973,"score_spread":0.1798698017803483,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W3110618962","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":[0.9995524,0.000102587255,0.000096059186,0.000020165866,0.0000033152699,0.000004954798,0.000036510373,0.0000051526067,0.00017878794],"genre_scores_gemma":[0.9995608,0.00005101615,0.0001595655,0.000019099136,0.000008524524,0.000002502198,0.000078028555,0.0000020439377,0.000118352036],"study_design_codex":"case_report","study_design_gemma":"observational","domain_scores_codex":[0.99983394,0.000017600312,0.000017171677,0.00005539544,0.00004956432,0.00002632753],"domain_scores_gemma":[0.9997156,0.000058958183,0.00011044439,0.000012334452,0.000026169473,0.00007637509],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00014382735,0.00038860828,0.00029937478,0.0005540969,0.00029984437,0.00016023735,0.00030614794,0.0006871354,0.0009188324],"category_scores_gemma":[0.0004955376,0.00014096533,0.00024798527,0.00036116302,0.00041974813,0.00013933469,0.0002802182,0.00024205205,0.00014001393],"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":[0.0007575967,0.00014464426,0.35321513,0.00021730881,0.00020047059,0.42827147,0.0013857591,0.0004231985,0.20601073,0.00030243842,0.00056955277,0.00850167],"study_design_scores_gemma":[0.000041787058,0.0004238389,0.7068795,0.000025249261,0.00008746252,0.2848466,0.00025015834,0.0011328442,0.005151549,0.000109879424,0.0010302032,0.000020907653],"about_ca_topic_score_codex":0.0021553228,"about_ca_topic_score_gemma":0.004153586,"teacher_disagreement_score":0.0021553228,"about_ca_system_score_codex":0.00027414004,"about_ca_system_score_gemma":0.00015375638,"threshold_uncertainty_score":0.0042855144},"labels":[],"label_agreement":null},{"id":"W3119356951","doi":"10.1186/s12883-020-02040-4","title":"Mild cognitive impairment in novel SPG11 mutation-related sporadic hereditary spastic paraplegia with thin corpus callosum: case series","year":2021,"lang":"en","type":"article","venue":"BMC Neurology","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":10,"is_retracted":false,"has_abstract":true,"route_ca_aff":false,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":true,"ca_institutions":"","funders":"National Natural Science Foundation of China","keywords":"Hereditary spastic paraplegia; Medicine; Cognition; Corpus callosum; Montreal Cognitive Assessment; Cognitive impairment; Pediatrics; Psychiatry; Pathology; Genetics; Phenotype; Biology; Gene","score_opus":0.03468915193554006,"score_gpt":0.256112748752655,"score_spread":0.22142359681711493,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W3119356951","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":[0.9962894,0.0010533645,0.0006426226,0.00017164466,0.00004019664,0.00007599373,0.00012888292,0.000039550207,0.0015584064],"genre_scores_gemma":[0.9983911,0.00049580476,0.00040788867,0.00012523869,0.00010781157,0.000018865256,0.0001111818,0.000011786362,0.00033025653],"study_design_codex":"case_report","study_design_gemma":"case_report","domain_scores_codex":[0.9995708,0.000031655283,0.000058318452,0.00016665031,0.00006320237,0.00010947638],"domain_scores_gemma":[0.99904996,0.00018148359,0.00021410725,0.00011510754,0.00012171817,0.00031761665],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0002605315,0.0016760654,0.00091336534,0.0017805599,0.0017314381,0.0009929622,0.0010652203,0.001773834,0.0015566457],"category_scores_gemma":[0.0019229659,0.00069345837,0.0007747437,0.0009796264,0.001468579,0.00066027755,0.0010405846,0.0010119901,0.0004062711],"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":[0.000092788265,0.00009967952,0.04266069,0.0000807157,0.00006433621,0.9514736,0.00057825557,0.00011904868,0.001529968,0.00009189881,0.00040786192,0.002801155],"study_design_scores_gemma":[0.000015526604,0.000109324865,0.029911475,0.00001972892,0.00006762813,0.9684152,0.00017919387,0.00022167197,0.0005138044,0.00012336244,0.00040615164,0.000016865128],"about_ca_topic_score_codex":0.004078829,"about_ca_topic_score_gemma":0.005436229,"teacher_disagreement_score":0.004078829,"about_ca_system_score_codex":0.00088348804,"about_ca_system_score_gemma":0.00068513997,"threshold_uncertainty_score":0.008110166},"labels":[],"label_agreement":null},{"id":"W3119963803","doi":"10.3389/fneur.2020.604547","title":"Case Report: Calpainopathy Presenting After Bone Marrow Transplantation, With Studies of Donor Genetic Content in Various Tissue Types","year":2021,"lang":"en","type":"article","venue":"Frontiers in Neurology","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":19,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Kelowna General Hospital; University of Calgary","funders":"","keywords":"Context (archaeology); Medicine; Pathology; Bone marrow; Transplantation; Biology; Internal medicine","score_opus":0.03307722087872442,"score_gpt":0.257185419257361,"score_spread":0.22410819837863657,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W3119963803","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":[0.9729749,0.0061027827,0.005183936,0.003294439,0.0003724973,0.00030465904,0.00041547033,0.00026132734,0.011089875],"genre_scores_gemma":[0.99406576,0.001499494,0.0016024063,0.00078877894,0.0006580785,0.00003055338,0.000106802574,0.000023270934,0.0012249828],"study_design_codex":"case_report","study_design_gemma":"case_report","domain_scores_codex":[0.9994449,0.000043729808,0.00006121543,0.00019853258,0.00006840144,0.00018321973],"domain_scores_gemma":[0.9991217,0.00019104982,0.00022942382,0.000077690056,0.00004834681,0.0003318035],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00035319658,0.002688379,0.00131934,0.002389552,0.0035656386,0.0018103515,0.001117237,0.0046604597,0.0024399396],"category_scores_gemma":[0.0019904114,0.00085335504,0.0010620594,0.001742097,0.0017045245,0.0015607361,0.0017501061,0.0027428428,0.0008314256],"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":[0.000044462053,0.00003702335,0.0046402887,0.000022432827,0.000006687794,0.9931425,0.00017896757,0.000049079175,0.0006850852,0.00009615148,0.00013836706,0.00095894304],"study_design_scores_gemma":[0.000005587351,0.000028141745,0.0012585786,0.000006049698,0.000008686975,0.99804485,0.00006468594,0.000055741868,0.00023790533,0.00008439478,0.00020096231,0.0000043616833],"about_ca_topic_score_codex":0.0026450485,"about_ca_topic_score_gemma":0.0030956138,"teacher_disagreement_score":0.0046604597,"about_ca_system_score_codex":0.0012798364,"about_ca_system_score_gemma":0.00068556616,"threshold_uncertainty_score":0.009285867},"labels":[],"label_agreement":null},{"id":"W3120763317","doi":"10.1017/cjn.2020.277","title":"Genetic and Epidemiological Study of Adult Ataxia and Spastic Paraplegia in Eastern Quebec","year":2021,"lang":"en","type":"article","venue":"Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":11,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":true,"route_about_ca":true,"ca_institutions":"McGill University; Centre hospitalier universitaire de Québec; Montreal Neurological Institute and Hospital; Université Laval","funders":"","keywords":"Hereditary spastic paraplegia; Ataxia; Medicine; Epidemiology; Confidence interval; Spastic; Allele frequency; Cerebellar ataxia; Allele; Internal medicine; Pediatrics; Genetics; Gene; Biology; Physical therapy; Phenotype; Psychiatry; Cerebral palsy","score_opus":0.05453617091566726,"score_gpt":0.2836079110754483,"score_spread":0.22907174015978105,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W3120763317","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":[0.99306595,0.0007180615,0.00033417254,0.00021821658,0.00000847994,0.000053299445,0.0043397946,0.00001222069,0.0012498118],"genre_scores_gemma":[0.9981572,0.0001857297,0.0002061021,0.000056455654,0.000004414878,0.000017376908,0.00094821246,0.0000019461854,0.00042255214],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99942756,0.00009032932,0.000047539554,0.00012334409,0.00019618007,0.000115011986],"domain_scores_gemma":[0.9980324,0.00015833635,0.0005293091,0.000053589712,0.0009045507,0.00032180207],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0007124063,0.00028259098,0.00029888938,0.0012616304,0.001191028,0.0005894633,0.00070299226,0.00037263715,0.0020026623],"category_scores_gemma":[0.0016666411,0.00015240446,0.0002644261,0.0023982602,0.00036453374,0.00025307384,0.00033780307,0.00039171244,0.00014983298],"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":[0.000022734914,0.000017333989,0.9976279,0.00001509808,0.000045191013,0.00005691591,0.00013959027,0.00007980398,0.00016233421,0.00003757534,0.0003749603,0.0014205332],"study_design_scores_gemma":[0.000003921352,0.000017760018,0.99918574,0.00001337616,0.000008217622,0.0000624112,0.00013769142,0.00025192046,0.000019544033,0.000005205516,0.00029175053,0.0000025206004],"about_ca_topic_score_codex":0.9669361,"about_ca_topic_score_gemma":0.9606663,"teacher_disagreement_score":0.03306389,"about_ca_system_score_codex":0.0074925534,"about_ca_system_score_gemma":0.0045379447,"threshold_uncertainty_score":0.066517174},"labels":[],"label_agreement":null},{"id":"W3122558558","doi":"10.1101/2021.01.14.425874","title":"Integrating protein networks and machine learning for disease stratification in the Hereditary Spastic Paraplegias","year":2021,"lang":"en","type":"preprint","venue":"bioRxiv (Cold Spring Harbor Laboratory)","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":0,"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 College London Hospitals NHS Foundation Trust; University College London; Engineering and Physical Sciences Research Council; UK Dementia Research Institute; National Institute for Health and Care Research; Weston Brain Institute; Alzheimer's Society; Wellcome Trust; Medical Research Council; Alzheimer's Association; Biotechnology and Biological Sciences Research Council; Michael J. Fox Foundation for Parkinson's Research","keywords":"Hereditary spastic paraplegia; Phenotype; Spasticity; Disease; Identification (biology); Medicine; Computational biology; Biology; Bioinformatics; Gene; Neuroscience; Genetics; Physical medicine and rehabilitation; Pathology","score_opus":0.031219153302134487,"score_gpt":0.2343823238799001,"score_spread":0.20316317057776562,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W3122558558","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":[0.7666261,0.0017863398,0.22605474,0.0010439465,0.000046358346,0.000113403534,0.0010584377,0.000681913,0.0025888127],"genre_scores_gemma":[0.9648263,0.00025328068,0.03409186,0.000030990293,0.000022729422,0.000030840576,0.00046158166,0.000012964514,0.00026951334],"study_design_codex":"simulation_or_modeling","study_design_gemma":"simulation_or_modeling","domain_scores_codex":[0.9996213,0.0002228633,0.00002001493,0.00006111843,0.000045474404,0.000029140276],"domain_scores_gemma":[0.99902856,0.0006308468,0.00013671542,0.000057664805,0.00008781956,0.0000584789],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0013843589,0.00050155376,0.00037598927,0.002951952,0.00023099799,0.00085468916,0.00022528012,0.00036034125,0.0006106537],"category_scores_gemma":[0.0023693654,0.00013604283,0.0004354732,0.0009782414,0.0003487359,0.00057199894,0.00047289615,0.00040549008,0.0001649031],"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":[0.0011336812,0.0005428693,0.18247288,0.00031989117,0.0007061867,0.00063020684,0.00023013272,0.52782536,0.033404615,0.013410456,0.0019641924,0.23735948],"study_design_scores_gemma":[0.000013577587,0.00007159497,0.021216344,0.000024541045,0.000051129984,0.000107057764,0.000045901907,0.9605745,0.0023160365,0.015163082,0.00040444097,0.0000117604],"about_ca_topic_score_codex":0.0015104099,"about_ca_topic_score_gemma":0.0015878637,"teacher_disagreement_score":0.002951952,"about_ca_system_score_codex":0.0005188252,"about_ca_system_score_gemma":0.00035481263,"threshold_uncertainty_score":0.007321298},"labels":[],"label_agreement":null},{"id":"W3123370243","doi":"10.1101/2021.01.14.21249305","title":"<i>GCH1</i> mutations in hereditary spastic paraplegia","year":2021,"lang":"en","type":"preprint","venue":"medRxiv","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":0,"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; Montreal Neurological Institute and Hospital; SickKids Foundation; University of Toronto; McGill University; Hospital for Sick Children","funders":"Fonds de Recherche du Québec - Santé; Canadian Institutes of Health Research; Parkinson Canada","keywords":"Hereditary spastic paraplegia; Hyperphenylalaninemia; Dystonia; Parkinsonism; Exome sequencing; Hyperreflexia; Levodopa; Spasticity; Genetics; Monozygotic twin; Spastic; Genetic heterogeneity; Medicine; Mutation; Phenotype; Disease; Biology; Gene; Internal medicine; Parkinson's disease; Neuroscience; Psychiatry; Physical therapy","score_opus":0.04956754394743685,"score_gpt":0.2811933305661481,"score_spread":0.23162578661871125,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W3123370243","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":[0.99551326,0.001007099,0.00036504827,0.00015166942,0.000018154242,0.000031199183,0.000727968,0.000031774205,0.0021538064],"genre_scores_gemma":[0.9984542,0.00022545681,0.00036456264,0.000118615266,0.0000114456225,0.0000044312997,0.000345632,0.000006714176,0.0004689493],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99989974,0.000008527147,0.000010134391,0.000027356857,0.000030148902,0.000024088984],"domain_scores_gemma":[0.99985445,0.000030336761,0.000026867938,0.000005823303,0.000034180764,0.000048350572],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.000103559716,0.0004729863,0.000274739,0.0007370635,0.00057154713,0.00029099194,0.00022826824,0.000341008,0.0023554035],"category_scores_gemma":[0.0003940441,0.00009087117,0.00021157709,0.0005980252,0.00028138465,0.00006786215,0.00021678783,0.0002085259,0.00026030059],"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":[0.0017899548,0.0001996558,0.6901698,0.0002997896,0.00038097036,0.062900625,0.0007824716,0.0014708301,0.18090516,0.00048427374,0.004893649,0.055722896],"study_design_scores_gemma":[0.00007260948,0.00018521721,0.92835134,0.000076900506,0.00025875404,0.040713593,0.00033609587,0.0011630981,0.022601718,0.0002588429,0.005963032,0.000018772489],"about_ca_topic_score_codex":0.03407683,"about_ca_topic_score_gemma":0.05960605,"teacher_disagreement_score":0.03407683,"about_ca_system_score_codex":0.0007149139,"about_ca_system_score_gemma":0.0005807904,"threshold_uncertainty_score":0.06775701},"labels":[],"label_agreement":null},{"id":"W3124703025","doi":"10.3174/ajnr.a7017","title":"Spinal Cord Gray and White Matter Damage in Different Hereditary Spastic Paraplegia Subtypes","year":2021,"lang":"en","type":"article","venue":"American Journal of Neuroradiology","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":17,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Calgary","funders":"Coordenação de Aperfeiçoamento de Pessoal de Nível Superior; Fundação de Amparo à Pesquisa do Estado de São Paulo","keywords":"Medicine; Paraplegia; Spinal cord; Hereditary spastic paraplegia; Spastic; Atrophy; White matter; Grey matter; Magnetic resonance imaging; Pathology; Radiology; Physical medicine and rehabilitation; Cerebral palsy; Phenotype","score_opus":0.021413570086909264,"score_gpt":0.2688042280627725,"score_spread":0.24739065797586324,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W3124703025","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":[0.99977726,0.000034053126,0.000021424607,0.0000053074546,5.1450365e-7,0.0000032401795,0.00006190494,0.000001297986,0.000095053205],"genre_scores_gemma":[0.99971694,0.000014430139,0.00004451719,0.000006636848,0.0000023027244,0.0000031386567,0.00015257196,0.0000012267899,0.000058260375],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99988544,0.000017915332,0.000016973676,0.000038034188,0.000018603274,0.000023069519],"domain_scores_gemma":[0.99956375,0.00006415676,0.00021149665,0.000025752815,0.00003855267,0.0000962078],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0002737825,0.00033115075,0.00025586734,0.0008127142,0.00033708324,0.0003034203,0.00018264922,0.00045822968,0.0017248745],"category_scores_gemma":[0.0007028181,0.00015775724,0.0002739031,0.00045209992,0.00036161885,0.00024149007,0.00031799014,0.0002195132,0.0001891692],"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":[0.00071546587,0.000039651593,0.990989,0.00001442647,0.00010092216,0.00076691987,0.00018080331,0.00011710447,0.004453575,0.0000292594,0.000090703004,0.0025021844],"study_design_scores_gemma":[0.000008208629,0.00006981308,0.9986131,0.0000025913585,0.000010851978,0.0009339725,0.00005559178,0.00010108449,0.00016024202,0.000019212628,0.00002365674,0.0000016252953],"about_ca_topic_score_codex":0.0054249903,"about_ca_topic_score_gemma":0.0071429885,"teacher_disagreement_score":0.0054249903,"about_ca_system_score_codex":0.0002959633,"about_ca_system_score_gemma":0.00015781802,"threshold_uncertainty_score":0.010786772},"labels":[],"label_agreement":null},{"id":"W3127282633","doi":"","title":"Familial Spastic Paraplegia and the ALS2 gene","year":2005,"lang":"en","type":"article","venue":"VUBIR (Vrije Universiteit Brussel)","topic":"Hereditary Neurological Disorders","field":"Neuroscience","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":"SickKids Foundation; Hospital for Sick Children","funders":"","keywords":"Hereditary spastic paraplegia; Paraplegia; Spastic; Physical medicine and rehabilitation; Medicine; Gene; Genetics; Neuroscience; Biology; Spinal cord; Cerebral palsy; Phenotype","score_opus":0.014966642486150546,"score_gpt":0.20236634423379446,"score_spread":0.18739970174764392,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W3127282633","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":[0.98788303,0.0033913022,0.0005386569,0.00076889416,0.00006477742,0.00001366176,0.00030320362,0.000040040457,0.0069963625],"genre_scores_gemma":[0.99706477,0.000524952,0.00023363777,0.00012755167,0.0000688672,0.0000062314334,0.00014530105,0.000009165014,0.0018195971],"study_design_codex":"case_report","study_design_gemma":"observational","domain_scores_codex":[0.9997098,0.00009662084,0.000027202967,0.000059120783,0.000047616737,0.000059630634],"domain_scores_gemma":[0.9996892,0.00011858475,0.000072761526,0.000015078775,0.000024791421,0.000079545876],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00023365926,0.0011956698,0.0005206036,0.0010951118,0.00076224376,0.00039978683,0.00032319696,0.0012841119,0.0041530556],"category_scores_gemma":[0.00080133457,0.00031929612,0.0002761105,0.00090539904,0.00062995224,0.0002543787,0.000599156,0.00043720144,0.00037656643],"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":[0.004211079,0.00045245112,0.105067745,0.0002780073,0.00039961952,0.81412643,0.0009580771,0.0010072661,0.050448827,0.00374552,0.0037976291,0.015507352],"study_design_scores_gemma":[0.0005413447,0.00082045153,0.3507491,0.00022982249,0.0004565965,0.6247578,0.00065001927,0.0021543968,0.008252368,0.0040714093,0.007245765,0.000070892755],"about_ca_topic_score_codex":0.0058740284,"about_ca_topic_score_gemma":0.004865681,"teacher_disagreement_score":0.0058740284,"about_ca_system_score_codex":0.0005046945,"about_ca_system_score_gemma":0.00043379233,"threshold_uncertainty_score":0.013893306},"labels":[],"label_agreement":null},{"id":"W3127311419","doi":"10.1002/mds.28519","title":"Brain Damage and Gene Expression Across Hereditary Spastic Paraplegia Subtypes","year":2021,"lang":"en","type":"article","venue":"Movement Disorders","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":28,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Calgary","funders":"Coordenação de Aperfeiçoamento de Pessoal de Nível Superior; Fundação de Amparo à Pesquisa do Estado de São Paulo","keywords":"Hereditary spastic paraplegia; Cerebellum; White matter; Pathology; Neuroscience; Atrophy; Biology; Medicine; Gene; Genetics; Phenotype; Magnetic resonance imaging","score_opus":0.020291669622962336,"score_gpt":0.2655924063095929,"score_spread":0.24530073668663058,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W3127311419","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":[0.99936336,0.00008580357,0.00007821927,0.0000068828595,7.0782784e-7,0.0000029799726,0.00032231392,0.00000389579,0.00013581761],"genre_scores_gemma":[0.9991359,0.000058291298,0.00011053277,0.000006389753,0.000001633034,0.000005923232,0.0005944522,0.0000037031202,0.00008315006],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9998172,0.0000223286,0.000019746682,0.000084014326,0.00003043996,0.000026271835],"domain_scores_gemma":[0.9995505,0.00005777907,0.00022807802,0.00004071279,0.000056872494,0.00006601409],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00030515628,0.00032130175,0.00023838301,0.0010969318,0.00023291323,0.00038105805,0.00018428995,0.00027990845,0.0014685225],"category_scores_gemma":[0.0007171151,0.00012315689,0.000247256,0.00079230085,0.00028972825,0.00015290313,0.00038434134,0.00016848462,0.00020501744],"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":[0.0004882083,0.00002797056,0.9776374,0.00003949612,0.00026501817,0.00044406787,0.0002339578,0.00024869601,0.015944192,0.000056576013,0.0001836172,0.0044307755],"study_design_scores_gemma":[0.0000025441097,0.000037740778,0.9988023,0.0000046766795,0.000025443973,0.0005028899,0.000057508696,0.00012263608,0.00033220425,0.000042846572,0.00006772349,0.0000014259095],"about_ca_topic_score_codex":0.0015694541,"about_ca_topic_score_gemma":0.0025034249,"teacher_disagreement_score":0.0015694541,"about_ca_system_score_codex":0.00015946564,"about_ca_system_score_gemma":0.000094343784,"threshold_uncertainty_score":0.0049126744},"labels":[],"label_agreement":null},{"id":"W3127489993","doi":"10.26443/mjm.v5i2.748","title":"Progressive Limb Weakness and Sensory Loss in a Young Woman","year":2020,"lang":"en","type":"article","venue":"McGill Journal of Medicine","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":0,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":true,"route_about_ca":false,"ca_institutions":"Montreal Neurological Institute and Hospital; McGill University","funders":"McGill University","keywords":"Medicine; Differential diagnosis; Weakness; Physical medicine and rehabilitation; Disease; Pediatrics; Intensive care medicine; Pathology; Surgery","score_opus":0.060405791709473154,"score_gpt":0.29515913286198536,"score_spread":0.2347533411525122,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W3127489993","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":[0.9385428,0.0039372067,0.0014840584,0.012361748,0.0009516779,0.00032312147,0.00063376944,0.00021252672,0.041553136],"genre_scores_gemma":[0.9830374,0.0019317244,0.0007285796,0.0042559304,0.0005590694,0.00003830206,0.00017803322,0.000032510994,0.009238405],"study_design_codex":"case_report","study_design_gemma":"case_report","domain_scores_codex":[0.9996915,0.000030893887,0.000023875631,0.00009406288,0.00005168565,0.00010807859],"domain_scores_gemma":[0.99957544,0.00007279933,0.000052692954,0.00001760637,0.000035168392,0.0002463211],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00023964689,0.0013053785,0.00066928734,0.0019360819,0.0020332818,0.00081604416,0.0008907706,0.0030645079,0.0027862752],"category_scores_gemma":[0.0015971686,0.0007958505,0.00059214554,0.0010012706,0.0009933733,0.0011155737,0.001046162,0.0019834295,0.0011553697],"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":[0.000015813004,0.00006183424,0.0053177387,0.000010828154,0.0000038135154,0.9920421,0.00022868648,0.000034273788,0.00043696287,0.00015962347,0.0007082124,0.0009801225],"study_design_scores_gemma":[0.000015083124,0.00018967043,0.026191039,0.00003554749,0.00001288296,0.9709711,0.0003453742,0.00020588827,0.00016199733,0.00023739983,0.001613363,0.000020611427],"about_ca_topic_score_codex":0.009392679,"about_ca_topic_score_gemma":0.016001187,"teacher_disagreement_score":0.009392679,"about_ca_system_score_codex":0.0012513561,"about_ca_system_score_gemma":0.0010547483,"threshold_uncertainty_score":0.018676043},"labels":[],"label_agreement":null},{"id":"W3130496612","doi":"10.1152/ajpcell.00594.2020","title":"Temporal manipulation of KCC3 expression in juvenile or adult mice suggests irreversible developmental deficit in hereditary motor sensory neuropathy with agenesis of the corpus callosum","year":2021,"lang":"en","type":"article","venue":"American Journal of Physiology-Cell Physiology","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":2,"is_retracted":false,"has_abstract":true,"route_ca_aff":false,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":true,"ca_institutions":"","funders":"National Institute of Neurological Disorders and Stroke; Eunice Kennedy Shriver National Institute of Child Health and Human Development; National Institute of Diabetes and Digestive and Kidney Diseases","keywords":"Hereditary motor and sensory neuropathy; Agenesis of the corpus callosum; Juvenile; Biology; Disease; Neuroscience; Corpus callosum; Internal medicine; Medicine; Genetics","score_opus":0.019260065657682863,"score_gpt":0.22868794394187356,"score_spread":0.20942787828419068,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W3130496612","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":[0.9891606,0.001196127,0.0034286533,0.00026368027,0.0000704171,0.00010334409,0.0021707772,0.00032435486,0.0032820862],"genre_scores_gemma":[0.9742656,0.001318042,0.005604051,0.00032123865,0.000019586436,0.00021751875,0.0014532185,0.00021897507,0.01658177],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99965453,0.00002249427,0.000031610027,0.00011250676,0.000085232554,0.0000937146],"domain_scores_gemma":[0.99954385,0.000042473635,0.00015970164,0.000041092095,0.00005052,0.00016234441],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00020127343,0.0005684892,0.00025731904,0.00080380094,0.0005201894,0.00036067032,0.00049346854,0.00071969413,0.002295555],"category_scores_gemma":[0.00014332175,0.0003355115,0.00041487144,0.00028146943,0.0007508569,0.0003005877,0.00031650419,0.0013884413,0.0006624597],"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":[0.00008870525,0.00003961613,0.0003139094,0.000022784934,0.0000035909047,0.00020050466,0.00005008268,0.000030759147,0.99828416,0.00013465034,0.00006242141,0.00076888496],"study_design_scores_gemma":[0.000083441286,0.00076469145,0.036419593,0.000041341664,0.00005267743,0.0014866078,0.00017889355,0.0009348855,0.95358056,0.00010032875,0.0063255467,0.00003143246],"about_ca_topic_score_codex":0.014978472,"about_ca_topic_score_gemma":0.053841036,"teacher_disagreement_score":0.014978472,"about_ca_system_score_codex":0.0014498775,"about_ca_system_score_gemma":0.0009284207,"threshold_uncertainty_score":0.029782593},"labels":[],"label_agreement":null},{"id":"W3131082731","doi":"10.1002/mds.28528","title":"Evidence for Non‐Mendelian Inheritance in Spastic Paraplegia 7","year":2021,"lang":"en","type":"article","venue":"Movement Disorders","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":27,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":true,"ca_institutions":"University of Ottawa; McMaster University; Montreal Neurological Institute and Hospital; University of Toronto; Children's Hospital of Eastern Ontario; McGill University; University of Alberta; Université Laval","funders":"Fonds de Recherche du Québec - Santé; Canadian Institutes of Health Research; Faculty of Medicine, McGill University","keywords":"Genetics; Hereditary spastic paraplegia; Spinocerebellar ataxia; Genotype; Biology; Exome sequencing; Epistasis; Cohort; Spastic; Gene; Medicine; Mutation; Internal medicine; Phenotype","score_opus":0.09269983372981302,"score_gpt":0.31445394520920145,"score_spread":0.22175411147938842,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W3131082731","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":[0.9646967,0.007697597,0.0086534,0.0023977235,0.00026241082,0.00020524664,0.0030770646,0.00036463366,0.012645247],"genre_scores_gemma":[0.99405307,0.001979408,0.0018538324,0.00022843305,0.00011194144,0.000042327178,0.0008835591,0.000037071786,0.00081036426],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9963387,0.00080970814,0.00029979154,0.0009974119,0.0012477909,0.00030650894],"domain_scores_gemma":[0.9927666,0.0035539062,0.0015492823,0.0006715533,0.0010620902,0.0003966138],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0024695965,0.0011916811,0.0007538286,0.0031352632,0.0008628536,0.0009240796,0.0014630605,0.0009827941,0.0130670825],"category_scores_gemma":[0.008279985,0.00036395926,0.00088890153,0.0025969108,0.0015155048,0.0002986225,0.0006384444,0.0006040343,0.00064834417],"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":[0.001426502,0.00015202908,0.9094971,0.0008098106,0.0023964625,0.02677223,0.0009511913,0.00057844864,0.009554535,0.0059506497,0.005015513,0.036895566],"study_design_scores_gemma":[0.00034062687,0.00038428832,0.9123072,0.00039366152,0.0012431733,0.06933794,0.00051753334,0.0024196599,0.0016996118,0.004210569,0.0070739,0.000071828166],"about_ca_topic_score_codex":0.022378298,"about_ca_topic_score_gemma":0.014605914,"teacher_disagreement_score":0.022378298,"about_ca_system_score_codex":0.000844347,"about_ca_system_score_gemma":0.0017132661,"threshold_uncertainty_score":0.04449606},"labels":[],"label_agreement":null},{"id":"W3135897702","doi":"10.1111/cge.13955","title":"<scp> <i>GCH1</i> </scp> mutations in hereditary spastic paraplegia","year":2021,"lang":"en","type":"article","venue":"Clinical Genetics","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":9,"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; Montreal Neurological Institute and Hospital; SickKids Foundation; University of Toronto; McGill University; Hospital for Sick Children","funders":"Fonds de Recherche du Québec - Santé; Canadian Institutes of Health Research","keywords":"Hereditary spastic paraplegia; Paraplegia; Spastic; Genetics; Mutation; Medicine; Neuroscience; Biology; Phenotype; Physical medicine and rehabilitation; Gene; Spinal cord; Cerebral palsy","score_opus":0.10210168368827051,"score_gpt":0.35389581385692354,"score_spread":0.25179413016865304,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W3135897702","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":[0.9962696,0.0005470978,0.00045547812,0.00009456735,0.000007980335,0.000030550174,0.00066241244,0.000025779907,0.0019064886],"genre_scores_gemma":[0.9980451,0.00026720174,0.0006261168,0.000081320664,0.0000054475936,0.000006831328,0.00044380547,0.000008646717,0.0005155427],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99991417,0.000007755109,0.000007973541,0.00002348037,0.000026288944,0.000020288251],"domain_scores_gemma":[0.99991,0.000018422883,0.000019828663,0.0000040161817,0.000018474875,0.000029304643],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00009983383,0.00043711314,0.00021619705,0.00061939395,0.0006665898,0.00032035875,0.00021808875,0.0002670598,0.0022250048],"category_scores_gemma":[0.00036104064,0.00009737152,0.0001863025,0.0006625866,0.00033031992,0.00007321838,0.0002742023,0.00020119303,0.0002404234],"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":[0.0015037641,0.00021819305,0.6534647,0.0003259533,0.00038902162,0.07546266,0.0016142683,0.001671446,0.16364428,0.00082160626,0.0052684965,0.095615655],"study_design_scores_gemma":[0.00006538137,0.00015272916,0.91312945,0.00007810818,0.00019014702,0.056003045,0.00041014006,0.0011896063,0.022761157,0.0003577931,0.0056438944,0.000018559946],"about_ca_topic_score_codex":0.054093733,"about_ca_topic_score_gemma":0.104715146,"teacher_disagreement_score":0.054093733,"about_ca_system_score_codex":0.00074518524,"about_ca_system_score_gemma":0.0007490712,"threshold_uncertainty_score":0.107557714},"labels":[],"label_agreement":null},{"id":"W3154061776","doi":"10.1101/2021.04.16.440179","title":"Developmental regulation of neuronal gene expression by Elongator complex protein 1 dosage","year":2021,"lang":"en","type":"preprint","venue":"bioRxiv (Cold Spring Harbor Laboratory)","topic":"Hereditary Neurological Disorders","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":"Medical Research Council; Cancer Research UK; York University; National Institutes of Health; Francis Crick Institute","keywords":"Biology; Gene; Phenotype; Cell biology; Transgene; Genetics; Embryonic stem cell; Gene expression; Regulation of gene expression; Mutation","score_opus":0.030792411808748626,"score_gpt":0.22482353270711944,"score_spread":0.19403112089837082,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W3154061776","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":[0.9914894,0.0017333627,0.0033273706,0.00007054131,0.000028735296,0.00002200975,0.0015773231,0.0001186956,0.0016324592],"genre_scores_gemma":[0.9885421,0.00096056267,0.0023615242,0.000082776576,0.0000075912594,0.00007437026,0.0017168056,0.000105166735,0.006149184],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9998266,0.000014071461,0.000018626195,0.00006656977,0.00003875936,0.000035489353],"domain_scores_gemma":[0.9998018,0.00003393592,0.00006256271,0.00002284738,0.000026481142,0.000052422114],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.000094786184,0.00026195345,0.00019057372,0.0004914562,0.00014760224,0.00037426077,0.000248633,0.00024211254,0.0012633518],"category_scores_gemma":[0.00014601593,0.00020235794,0.00022302476,0.00019440842,0.00022363034,0.00019041204,0.00033693385,0.0005269703,0.00035142922],"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":[0.000046724777,0.00000533617,0.00030593615,0.000012054087,0.000003024826,0.000023100109,0.000008614192,0.000025825784,0.9988776,0.000043232358,0.000019764262,0.0006287914],"study_design_scores_gemma":[0.000007888076,0.000071929404,0.02779972,0.000011600936,0.000020721178,0.00013814693,0.000056492503,0.0009508841,0.9689006,0.00006305651,0.0019713705,0.0000076248957],"about_ca_topic_score_codex":0.00096404314,"about_ca_topic_score_gemma":0.0015728732,"teacher_disagreement_score":0.0012633518,"about_ca_system_score_codex":0.0005632403,"about_ca_system_score_gemma":0.00018504816,"threshold_uncertainty_score":0.004226327},"labels":[],"label_agreement":null},{"id":"W3155801020","doi":"10.1212/wnl.96.15_supplement.2100","title":"GCH1 Mutations in Hereditary Spastic Paraplegia (2100)","year":2021,"lang":"en","type":"article","venue":"Neurology","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":false,"ca_institutions":"Université Laval; Montreal Neurological Institute and Hospital; SickKids Foundation; University of Toronto; McGill University; Hospital for Sick Children","funders":"","keywords":"Hereditary spastic paraplegia; Paraplegia; Medicine; Spastic; Mutation; Genetics; Biology; Physical medicine and rehabilitation; Spinal cord; Phenotype; Gene; Cerebral palsy; Psychiatry","score_opus":0.034677372195417895,"score_gpt":0.2698347882061312,"score_spread":0.23515741601071333,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W3155801020","genre_codex":"empirical","genre_gemma":"other","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"other","genre_consensus":null,"domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9691672,0.0011151806,0.0004360767,0.0005451476,0.00019426837,0.000038159014,0.0012999354,0.000079358615,0.027124783],"genre_scores_gemma":[0.99534696,0.00019669,0.00045292743,0.00019715085,0.000052656476,0.000007071928,0.00037619384,0.000018982273,0.0033513342],"study_design_codex":"case_report","study_design_gemma":"not_applicable","domain_scores_codex":[0.99989176,0.000008184809,0.000015508518,0.00002789745,0.000026499894,0.000030232157],"domain_scores_gemma":[0.99980825,0.000042426767,0.000040964864,0.0000074167638,0.000035473815,0.00006541824],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.000117938886,0.00075898605,0.00023699494,0.0009132595,0.0007625762,0.00037368358,0.00041233812,0.0010412242,0.005938344],"category_scores_gemma":[0.0005933243,0.00015609692,0.00030937308,0.0007167312,0.00038377513,0.00019409653,0.0005057139,0.00022791528,0.001065296],"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":[0.0018450667,0.00028377495,0.16781084,0.00029278544,0.00020620134,0.6400523,0.0012794709,0.0010922842,0.13141344,0.003669749,0.012381831,0.03967225],"study_design_scores_gemma":[0.00025273077,0.0005437386,0.3239312,0.0002643932,0.00037432637,0.58880293,0.0006809994,0.002620163,0.045476146,0.0025972053,0.03434052,0.00011568971],"about_ca_topic_score_codex":0.009216961,"about_ca_topic_score_gemma":0.010895569,"teacher_disagreement_score":0.009216961,"about_ca_system_score_codex":0.0005588034,"about_ca_system_score_gemma":0.0006035233,"threshold_uncertainty_score":0.019865751},"labels":[],"label_agreement":null},{"id":"W3156481006","doi":"10.1111/jnc.15365","title":"Neuronally expressed a‐series gangliosides are sufficient to prevent the lethal age‐dependent phenotype in GM3‐only expressing mice","year":2021,"lang":"en","type":"article","venue":"Journal of Neurochemistry","topic":"Hereditary Neurological Disorders","field":"Neuroscience","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":"Institute of Infection and Immunity","funders":"Wellcome Trust","keywords":"Ganglioside; Neurodegeneration; Biology; Phenotype; Cell biology; Node of Ranvier; Transgene; Nervous system; Central nervous system; Genetically modified mouse; Immunology; Axon; Molecular biology; Neuroscience; Biochemistry; Internal medicine; Gene; Myelin; Medicine","score_opus":0.027850615766089836,"score_gpt":0.2614439197767644,"score_spread":0.23359330401067457,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W3156481006","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":[0.9875224,0.0008182113,0.0043515153,0.0003244548,0.00012124047,0.00022989589,0.0033306207,0.00081208785,0.0024894837],"genre_scores_gemma":[0.9599715,0.0014277983,0.008693569,0.00029709737,0.00006504181,0.00052970607,0.0036127726,0.0005702589,0.024832265],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9995153,0.000040354185,0.000083854015,0.00011618686,0.0001168683,0.00012736254],"domain_scores_gemma":[0.99902606,0.000077212426,0.00031700658,0.00008845132,0.00008633571,0.0004049027],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00031560985,0.0013349525,0.00063188875,0.001169615,0.00046219962,0.0006189405,0.0007811572,0.0013518834,0.0033330224],"category_scores_gemma":[0.00021349432,0.00055009464,0.0007273927,0.0002883012,0.00095377973,0.0005840757,0.0005820853,0.0025119367,0.0018697743],"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":[0.00016268175,0.00008671761,0.00008511751,0.00002835593,0.000008167933,0.000063377374,0.000024656743,0.00004254542,0.99895275,0.00010539446,0.000045263972,0.000394847],"study_design_scores_gemma":[0.00008879149,0.0007880482,0.0031515483,0.000031796313,0.000037018068,0.0003696563,0.00006904248,0.0009863252,0.99128073,0.000100576704,0.0030799005,0.000016728114],"about_ca_topic_score_codex":0.0018851812,"about_ca_topic_score_gemma":0.0027415531,"teacher_disagreement_score":0.0033330224,"about_ca_system_score_codex":0.0006820789,"about_ca_system_score_gemma":0.00065770536,"threshold_uncertainty_score":0.011150122},"labels":[],"label_agreement":null},{"id":"W3157413169","doi":"10.1016/j.isci.2021.102484","title":"Integrating protein networks and machine learning for disease stratification in the Hereditary Spastic Paraplegias","year":2021,"lang":"en","type":"article","venue":"iScience","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":10,"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":"Engineering and Physical Sciences Research Council; Medical Research Council; University College London; Rosetrees Trust; University College London Hospitals NHS Foundation Trust; Parkinson's UK; UK Dementia Research Institute; National Institute for Health and Care Research; Weston Brain Institute; Alzheimer's Society; Wellcome Trust; Alzheimer's Association; Biotechnology and Biological Sciences Research Council; Michael J. Fox Foundation for Parkinson's Research","keywords":"Hereditary spastic paraplegia; Computational biology; Phenotype; Neuroscience; Disease; Medicine; Biology; Bioinformatics; Gene; Genetics; Pathology","score_opus":0.04839127309575603,"score_gpt":0.27327178630589866,"score_spread":0.22488051321014263,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W3157413169","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":[0.7244436,0.003389048,0.2663583,0.0010049229,0.000041576972,0.00013928104,0.0010136574,0.0005618143,0.003047753],"genre_scores_gemma":[0.9635775,0.00046532918,0.035110004,0.00003228276,0.00002177667,0.00003409049,0.0005169885,0.000010157967,0.00023184031],"study_design_codex":"simulation_or_modeling","study_design_gemma":"simulation_or_modeling","domain_scores_codex":[0.9994925,0.00030471705,0.000031144365,0.0000743791,0.0000589434,0.000038248792],"domain_scores_gemma":[0.9989324,0.0007496398,0.00012385761,0.00005796608,0.0000834001,0.000052775897],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0015926636,0.0005175203,0.0004150534,0.0033642794,0.00026726408,0.00090155366,0.00024285674,0.00034036784,0.000537323],"category_scores_gemma":[0.0029817459,0.0001291622,0.00043160107,0.0011169151,0.000400068,0.00074730336,0.0005119679,0.00040000316,0.00016079983],"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":[0.0012042302,0.000457712,0.20979464,0.0003251304,0.0006551224,0.00065846345,0.0003016404,0.44617954,0.021126477,0.014516889,0.0013529644,0.30342722],"study_design_scores_gemma":[0.000017707775,0.00011057189,0.036120713,0.000043680906,0.00009282591,0.00024696064,0.000097820855,0.9338354,0.002232074,0.02642481,0.00075553777,0.000021872833],"about_ca_topic_score_codex":0.0018944481,"about_ca_topic_score_gemma":0.0024843295,"teacher_disagreement_score":0.0033642794,"about_ca_system_score_codex":0.00054055254,"about_ca_system_score_gemma":0.00041176428,"threshold_uncertainty_score":0.008422911},"labels":[],"label_agreement":null},{"id":"W3157716789","doi":"10.1212/wnl.96.15_supplement.4943","title":"Hereditary Spastic Paraplegia: Clinicogenetic Lessons from a Well-Defined Cohort (4943)","year":2021,"lang":"en","type":"article","venue":"Neurology","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":"Montreal Neurological Institute and Hospital; McGill University; University of Alberta Hospital; University of Calgary; University of Alberta","funders":"","keywords":"Hereditary spastic paraplegia; Spastic; Cohort; Paraplegia; Medicine; Physical medicine and rehabilitation; Business; Psychiatry; Spinal cord; Biology; Pathology; Cerebral palsy; Genetics","score_opus":0.04659511420618416,"score_gpt":0.2917804039722386,"score_spread":0.24518528976605442,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W3157716789","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":[0.99355835,0.0007410201,0.0005251185,0.00030209552,0.000021925633,0.00007459169,0.0013377918,0.000020013209,0.0034190665],"genre_scores_gemma":[0.9968167,0.00040267597,0.000510035,0.00023560299,0.000022636195,0.000030505216,0.0010885147,0.00002150598,0.00087198097],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9990613,0.000110693174,0.000057862482,0.00020633836,0.0002849425,0.0002788166],"domain_scores_gemma":[0.9987251,0.00012697297,0.000187109,0.00012329244,0.0004517809,0.0003856037],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0005942378,0.00079977943,0.0004580838,0.0016754741,0.0029783128,0.0012547337,0.0011092986,0.0005412329,0.0029568877],"category_scores_gemma":[0.0019417271,0.0002489385,0.00030353718,0.001944794,0.00077256246,0.00032562827,0.0010493242,0.00058197405,0.00045281564],"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":[0.00018317305,0.00013472294,0.97801936,0.000019615452,0.0000987843,0.004993328,0.0018585421,0.00015735455,0.0026795173,0.00054389174,0.0021455197,0.0091662165],"study_design_scores_gemma":[0.000024715882,0.00007494098,0.9888081,0.000028625738,0.00007154548,0.0062687714,0.0015975705,0.00025807502,0.00026322057,0.00024919488,0.0023352008,0.000020008396],"about_ca_topic_score_codex":0.60842705,"about_ca_topic_score_gemma":0.76228946,"teacher_disagreement_score":0.60842705,"about_ca_system_score_codex":0.0038720714,"about_ca_system_score_gemma":0.0041747857,"threshold_uncertainty_score":0.787758},"labels":[],"label_agreement":null},{"id":"W3159781145","doi":"10.3389/fneur.2021.662353","title":"Editorial: Epidemiology of Atypical Demyelinating Diseases","year":2021,"lang":"en","type":"editorial","venue":"Frontiers in Neurology","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":2,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Toronto; St. Michael's Hospital","funders":"","keywords":"Medicine; Epidemiology; Front (military); Family medicine; Pathology; Geography","score_opus":0.022433351718363366,"score_gpt":0.29640023185166786,"score_spread":0.2739668801333045,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W3159781145","genre_codex":"editorial","genre_gemma":"editorial","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"editorial","genre_consensus":"editorial","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.000038277227,0.0035140724,0.00008293792,0.025875116,0.9692978,0.000019463774,0.000103100145,0.000054005544,0.0010152031],"genre_scores_gemma":[0.00034517687,0.002765782,0.000056190376,0.01168842,0.9812206,0.000017942557,0.000050404768,0.000021498425,0.0038341135],"study_design_codex":"not_applicable","study_design_gemma":"not_applicable","domain_scores_codex":[0.99650913,0.00064987113,0.00060256606,0.00049557723,0.0014977907,0.00024510294],"domain_scores_gemma":[0.9810007,0.006824716,0.001448885,0.00043046742,0.007432368,0.0028627643],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0060211527,0.0052750926,0.004223847,0.0052646217,0.0023899374,0.005763385,0.0038790263,0.010660967,0.018567786],"category_scores_gemma":[0.024677906,0.0012081554,0.002819293,0.001551468,0.0016471423,0.0048190965,0.0015265726,0.013242005,0.013710773],"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":[0.00004466623,0.000010314158,0.000037365902,0.00017580108,0.000023358623,0.0001199987,0.000007373173,0.000021104872,0.000025764837,0.000106686726,0.9958923,0.0035352337],"study_design_scores_gemma":[0.00019513961,0.000051701325,0.00070827076,0.0010123618,0.0001751609,0.00082390825,0.000069716734,0.0002741832,0.00015566523,0.0012727807,0.99521977,0.00004131722],"about_ca_topic_score_codex":0.0015650726,"about_ca_topic_score_gemma":0.0034843795,"teacher_disagreement_score":0.018567786,"about_ca_system_score_codex":0.0027674302,"about_ca_system_score_gemma":0.0021241615,"threshold_uncertainty_score":0.06211537},"labels":[],"label_agreement":null},{"id":"W3166727665","doi":"10.1101/2021.06.04.447086","title":"Selective retinal ganglion cell loss and optic neuropathy in a humanized mouse model of familial dysautonomia","year":2021,"lang":"en","type":"preprint","venue":"bioRxiv (Cold Spring Harbor Laboratory)","topic":"Hereditary Neurological Disorders","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":"Grousbeck Family Foundation; National Eye Institute; York University; Montana State University","keywords":"RNA splicing; Retinal degeneration; Exon; Biology; Familial dysautonomia; Retinal ganglion cell; Phenotype; Retinal; Humanized mouse; Dysautonomia; Neuroscience; Cell biology; Retina; Genetics; Gene; Disease; Medicine; Pathology; In vivo","score_opus":0.01921232976305636,"score_gpt":0.21274345218969912,"score_spread":0.19353112242664275,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W3166727665","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":[0.9829064,0.0016056878,0.007047681,0.0005794895,0.00017529953,0.00020742505,0.0024403692,0.0005162644,0.0045213513],"genre_scores_gemma":[0.9645314,0.0017021669,0.011087943,0.00027014056,0.00003328112,0.00042551674,0.0015752405,0.00016171478,0.020212518],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99955827,0.00006880215,0.000052135114,0.00013607647,0.00011661926,0.000068047935],"domain_scores_gemma":[0.9997919,0.00002238321,0.00007937422,0.00003054478,0.00001619766,0.000059530466],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0005518723,0.0011634816,0.00041693327,0.0017370417,0.00045808926,0.0004921685,0.0005296963,0.0011243465,0.002898412],"category_scores_gemma":[0.00013616728,0.00042204454,0.00055639877,0.00038741814,0.0008776041,0.00041514635,0.00044353207,0.0013127058,0.00076752383],"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":[0.00045206677,0.00027503405,0.00022957614,0.000053286934,0.00001983691,0.00053329865,0.00007020104,0.00015200982,0.9957657,0.00072343723,0.00024007802,0.0014854715],"study_design_scores_gemma":[0.00037901342,0.0020372404,0.0060251765,0.00006792693,0.000111317364,0.0031230825,0.00017580218,0.0028536546,0.97527814,0.00049313216,0.009427313,0.000028229793],"about_ca_topic_score_codex":0.0019661337,"about_ca_topic_score_gemma":0.0028199581,"teacher_disagreement_score":0.002898412,"about_ca_system_score_codex":0.00075136835,"about_ca_system_score_gemma":0.0005319415,"threshold_uncertainty_score":0.009696186},"labels":[],"label_agreement":null},{"id":"W3180105899","doi":"10.1002/pds.5326","title":"Uncommon side effects of common drugs in patients with familial dysautonomia","year":2021,"lang":"en","type":"article","venue":"Pharmacoepidemiology and Drug Safety","topic":"Hereditary Neurological Disorders","field":"Neuroscience","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","funders":"Dysautonomia Foundation","keywords":"Medicine; Adverse effect; Internal medicine; Dyscrasia; Side effect (computer science); Drug; Familial dysautonomia; Population; Pharmacology","score_opus":0.011676590478292103,"score_gpt":0.2678930666299456,"score_spread":0.2562164761516535,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W3180105899","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":[0.9962165,0.0022373598,0.00025444757,0.000048509446,0.000005222294,0.00001113054,0.00048074854,0.000011091576,0.00073494535],"genre_scores_gemma":[0.9987355,0.00042747328,0.00029903412,0.000057575307,0.000008212987,0.000006200085,0.00033878686,0.0000015471737,0.0001257142],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99963856,0.00006803991,0.00007338725,0.00009918459,0.0000860205,0.00003471134],"domain_scores_gemma":[0.99901664,0.00031329694,0.00050379813,0.000046732086,0.00005938936,0.000060112125],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0002988304,0.0001918953,0.00045470285,0.0005726186,0.00026809965,0.0002659053,0.000098493925,0.00022812463,0.0009828915],"category_scores_gemma":[0.0010660904,0.000075585136,0.00031509937,0.00077411265,0.00018264468,0.0001642506,0.00017620566,0.00020644451,0.000108388864],"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":[0.00040461076,0.000037406124,0.9776308,0.0001067656,0.00010601337,0.0014056758,0.000091969436,0.00008069426,0.00570797,0.000021954742,0.00013747493,0.014268618],"study_design_scores_gemma":[0.000007706283,0.00016266732,0.9930957,0.000013734528,0.00006280841,0.00502234,0.00005029836,0.000096606884,0.0010165651,0.000021967398,0.0004462429,0.0000034413297],"about_ca_topic_score_codex":0.0009663653,"about_ca_topic_score_gemma":0.0020585584,"teacher_disagreement_score":0.0009828915,"about_ca_system_score_codex":0.00023519748,"about_ca_system_score_gemma":0.00014211265,"threshold_uncertainty_score":0.0032880902},"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":"W3186444178","doi":"10.1101/2021.07.20.21259482","title":"Genetic, structural and clinical analysis of spastic paraplegia 4","year":2021,"lang":"en","type":"preprint","venue":"medRxiv","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":3,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":true,"ca_institutions":"University of Alberta; Université Laval; McGill University; University of Ottawa; Hospital for Sick Children; SickKids Foundation; Montreal Neurological Institute and Hospital; Université de Sherbrooke; University of Toronto; McMaster University; Alberta Children's Hospital; Children's Hospital of Eastern Ontario","funders":"Fonds de Recherche du Québec - Santé; Canadian Institutes of Health Research","keywords":"Hereditary spastic paraplegia; Genetics; Multiplex ligation-dependent probe amplification; Mutation; Genetic heterogeneity; Genotype; Copy-number variation; Biology; Exome sequencing; Gene; Compound heterozygosity; Medicine; Phenotype; Exon; Genome","score_opus":0.06694548282405961,"score_gpt":0.3375826976378737,"score_spread":0.2706372148138141,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W3186444178","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":[0.9971679,0.00029611788,0.00032589433,0.00006784236,0.000003933969,0.000014657115,0.000557803,0.000013282794,0.0015526406],"genre_scores_gemma":[0.9983772,0.00017671383,0.00036434995,0.000028322844,0.0000049234013,0.0000048573534,0.00042360308,0.000005179746,0.0006148433],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99984515,0.00001889156,0.00001492016,0.00003920456,0.000051553572,0.000030216797],"domain_scores_gemma":[0.99984,0.000037772967,0.000032713666,0.000008829814,0.000041725976,0.000038986025],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00016860162,0.00036724508,0.00024929788,0.00093237037,0.0004926928,0.00033552427,0.00022292887,0.00021193425,0.0032060454],"category_scores_gemma":[0.0006532478,0.000085594846,0.00016886258,0.00062954193,0.00031032338,0.000072853916,0.00036247878,0.000144815,0.00027321873],"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":[0.00063834485,0.00009451375,0.8224603,0.00020097547,0.000212173,0.036831733,0.0010104558,0.0010343465,0.08692331,0.00047412756,0.0014087955,0.048710894],"study_design_scores_gemma":[0.000031451396,0.00014559895,0.9443519,0.000047545345,0.00009567089,0.04084565,0.0004512868,0.00093065074,0.009868593,0.00021782143,0.003001789,0.00001197786],"about_ca_topic_score_codex":0.036582455,"about_ca_topic_score_gemma":0.031121084,"teacher_disagreement_score":0.036582455,"about_ca_system_score_codex":0.00070177537,"about_ca_system_score_gemma":0.0008007861,"threshold_uncertainty_score":0.072739065},"labels":[],"label_agreement":null},{"id":"W3186899036","doi":"10.1093/hmg/ddab207","title":"Effective therapeutic strategies in a preclinical mouse model of Charcot–Marie–Tooth disease","year":2021,"lang":"en","type":"article","venue":"Human Molecular 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":"Instituto de Salud Carlos III; Ministerio de Economía y Competitividad; Arnie Charbonneau Cancer Institute, University of Calgary","keywords":"Biology; Pharmacology; Gene knockdown; Oxidative stress; Antioxidant; Florfenicol; Cancer research; Antibiotics; Biochemistry; Apoptosis","score_opus":0.07187662447254675,"score_gpt":0.3349520023115582,"score_spread":0.26307537783901147,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W3186899036","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":[0.95630753,0.011335699,0.013839941,0.0022754888,0.0009653095,0.0009893157,0.0034128055,0.0012651158,0.0096087735],"genre_scores_gemma":[0.9427207,0.013059142,0.019541292,0.00082432985,0.000117470234,0.0016724662,0.003203723,0.00018002735,0.018680934],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99950767,0.000081723185,0.000049355163,0.00012411804,0.00013479016,0.00010234511],"domain_scores_gemma":[0.99977094,0.000026998585,0.00005421448,0.000027092005,0.000027289027,0.00009345703],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0006500927,0.0015676596,0.0008539847,0.0013412781,0.00066034205,0.0007396033,0.0009629509,0.0016447854,0.0022653241],"category_scores_gemma":[0.00024290424,0.00035524362,0.00067522866,0.00035842162,0.0008356049,0.0007277938,0.0004579869,0.002709531,0.0007136491],"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":[0.00058512215,0.0007116659,0.00011325027,0.00019317504,0.000033423632,0.00036933328,0.00006226737,0.00028176713,0.9918589,0.00084568287,0.0006547304,0.004290544],"study_design_scores_gemma":[0.0006206228,0.007723821,0.0023966504,0.00016988095,0.00018127332,0.0013594754,0.00014515259,0.0020239817,0.959715,0.00078076404,0.02483592,0.000047434627],"about_ca_topic_score_codex":0.0016591114,"about_ca_topic_score_gemma":0.0042976756,"teacher_disagreement_score":0.0022653241,"about_ca_system_score_codex":0.0008663978,"about_ca_system_score_gemma":0.0008035034,"threshold_uncertainty_score":0.0075783134},"labels":[],"label_agreement":null},{"id":"W3187439951","doi":"10.1111/jvim.16242","title":"Hereditary sensory and autonomic neuropathy in a family of mixed breed dogs associated with a novel <i>RETREG1</i> variant","year":2021,"lang":"en","type":"article","venue":"Journal of Veterinary Internal Medicine","topic":"Hereditary Neurological Disorders","field":"Neuroscience","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":"University of Calgary","funders":"University of Glasgow","keywords":"Breed; Medicine; Missense mutation; Sensory system; Pathology; Physiology; Genetics; Gene; Biology; Mutation; Neuroscience","score_opus":0.05455644772511454,"score_gpt":0.27364752787528734,"score_spread":0.2190910801501728,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W3187439951","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":[0.9989606,0.00009344854,0.0003545417,0.00006171879,0.000008989168,0.000008895939,0.000037007496,0.000015305593,0.00045955708],"genre_scores_gemma":[0.9992244,0.000047588306,0.00042446784,0.00005159045,0.000016703776,0.0000051500615,0.00007130232,0.0000053634353,0.00015338944],"study_design_codex":"case_report","study_design_gemma":"observational","domain_scores_codex":[0.9997261,0.000031264564,0.000022885446,0.00011976272,0.000056003915,0.00004396422],"domain_scores_gemma":[0.99968433,0.00008340447,0.00010601672,0.000014766478,0.00002563428,0.0000858579],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00027601232,0.0007569462,0.00035617556,0.000896915,0.0006349546,0.00039152525,0.00040921624,0.0006940723,0.0015258176],"category_scores_gemma":[0.0005698063,0.0003202015,0.0003704996,0.00038203507,0.0007285762,0.00030249084,0.00045983246,0.0004947395,0.0002124988],"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":[0.00067165896,0.0003692379,0.3705634,0.00014998532,0.00024189064,0.5285432,0.0019277352,0.00048161883,0.08498982,0.00043238475,0.00097037264,0.010658714],"study_design_scores_gemma":[0.00007547232,0.00084709906,0.31897485,0.000044409288,0.00017682182,0.66954374,0.0004378601,0.0015757611,0.005945409,0.00019287647,0.0021462862,0.000039356983],"about_ca_topic_score_codex":0.0007870241,"about_ca_topic_score_gemma":0.0013243253,"teacher_disagreement_score":0.0015258176,"about_ca_system_score_codex":0.00032233048,"about_ca_system_score_gemma":0.00014993102,"threshold_uncertainty_score":0.005104363},"labels":[],"label_agreement":null},{"id":"W3188061514","doi":"10.1017/cjn.2021.188","title":"Anticipation Can Be More Common in Hereditary Spastic Paraplegia with <i>SPAST</i> Mutations Than It Appears","year":2021,"lang":"en","type":"article","venue":"Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":10,"is_retracted":false,"has_abstract":true,"route_ca_aff":false,"route_ca_fund":false,"route_ca_venue":true,"route_about_ca":false,"ca_institutions":"","funders":"National Institute for Medical Research Development; University of Social Welfare and Rehabilitation Sciences","keywords":"Anticipation (artificial intelligence); Proband; Hereditary spastic paraplegia; Genetics; Multiplex ligation-dependent probe amplification; Genetic heterogeneity; Age of onset; Biology; Sanger sequencing; Phenotype; Gene; Disease; Mutation; Medicine; Internal medicine","score_opus":0.05283658112072994,"score_gpt":0.2870776240825339,"score_spread":0.23424104296180395,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W3188061514","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":[0.9973176,0.00041937808,0.0007978767,0.00006590055,0.0000169749,0.0000101976675,0.00012475257,0.00006129604,0.0011860154],"genre_scores_gemma":[0.9988953,0.0001507845,0.00039285154,0.000052105803,0.000034407694,0.000005669935,0.00017729453,0.000008575115,0.00028302957],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9997807,0.000042539283,0.000029264465,0.000060017588,0.000046289002,0.00004120596],"domain_scores_gemma":[0.9990048,0.00021172599,0.000574289,0.000049978316,0.000058048226,0.00010133827],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00024171398,0.0007082158,0.00029497006,0.0009740429,0.00029914113,0.00022119316,0.00022948481,0.00045877622,0.0037857634],"category_scores_gemma":[0.0010047609,0.00014185067,0.0003105039,0.0006133263,0.00037220863,0.00023069537,0.00033240204,0.00028767216,0.0005155779],"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":[0.0015239763,0.00018513197,0.7621896,0.00031155196,0.00022323,0.108954564,0.0005548154,0.00033025222,0.088409334,0.00073434017,0.0013347763,0.035248447],"study_design_scores_gemma":[0.00006763452,0.0007239333,0.6801617,0.00008275651,0.00020248903,0.29983643,0.00031338976,0.00057722774,0.012375912,0.0010316777,0.004587513,0.000039310857],"about_ca_topic_score_codex":0.0003890792,"about_ca_topic_score_gemma":0.00048180862,"teacher_disagreement_score":0.0037857634,"about_ca_system_score_codex":0.00011177698,"about_ca_system_score_gemma":0.00015337655,"threshold_uncertainty_score":0.012664616},"labels":[],"label_agreement":null},{"id":"W3193534589","doi":"10.7759/cureus.17201","title":"Impact of Customized and Sustained Physiotherapy in Charcot-Marie-Tooth Disease","year":2021,"lang":"en","type":"article","venue":"Cureus","topic":"Hereditary Neurological Disorders","field":"Neuroscience","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":"Royal College of Physicians and Surgeons of Canada","funders":"","keywords":"Medicine; Weakness; Peripheral neuropathy; Physical medicine and rehabilitation; Hereditary motor and sensory neuropathy; Forefoot; Muscle contracture; Polyneuropathy; Electromyography; Pes cavus; Physical therapy; Disease; Anatomy; Surgery; Pathology","score_opus":0.020609732946920846,"score_gpt":0.32001786257560977,"score_spread":0.2994081296286889,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W3193534589","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":[0.5165205,0.35893482,0.00094479596,0.031896666,0.0041933064,0.00020404994,0.0018775995,0.00014010545,0.08528819],"genre_scores_gemma":[0.9290455,0.05583173,0.0007935894,0.0051909047,0.0018626042,0.00007473494,0.0007464359,0.000026525557,0.0064279484],"study_design_codex":"design_other","study_design_gemma":"observational","domain_scores_codex":[0.99940205,0.00019155248,0.000058896425,0.00007857032,0.00017563014,0.00009340473],"domain_scores_gemma":[0.999311,0.00019666537,0.00008359737,0.000020787984,0.00011632285,0.00027162995],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0004353213,0.00034481293,0.00046887327,0.00034094302,0.00058229227,0.00051816466,0.00042481496,0.00069205643,0.007912096],"category_scores_gemma":[0.0017584899,0.000051590774,0.00088302733,0.0004609955,0.0001943784,0.00038928326,0.00048394545,0.0006809644,0.0005673498],"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":[0.004708747,0.0038296774,0.09072038,0.0035038253,0.0013531065,0.0177901,0.00056023255,0.0011523445,0.0031484421,0.0014011646,0.028117105,0.84371483],"study_design_scores_gemma":[0.0010782612,0.009186931,0.7793893,0.008983745,0.0025069749,0.041694414,0.0016829822,0.0018574727,0.0007787405,0.0033112704,0.1493798,0.00015001916],"about_ca_topic_score_codex":0.008186694,"about_ca_topic_score_gemma":0.012682754,"teacher_disagreement_score":0.008186694,"about_ca_system_score_codex":0.00089560787,"about_ca_system_score_gemma":0.0009446303,"threshold_uncertainty_score":0.026468635},"labels":[],"label_agreement":null},{"id":"W3199046023","doi":"10.1017/cjn.2021.217","title":"Radio-Pathologic Correlation of the “Pig’s Snout” Sign in Osmotic Demyelination Syndrome","year":2021,"lang":"en","type":"article","venue":"Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques","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":true,"route_about_ca":false,"ca_institutions":"London Health Sciences Centre","funders":"","keywords":"Sign (mathematics); Snout; Medicine; Anatomy; Pathology; Nuclear magnetic resonance; Neuroscience; Biology; Physics; Mathematics","score_opus":0.03844451476938324,"score_gpt":0.25675553175745797,"score_spread":0.21831101698807473,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W3199046023","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":[0.98333156,0.0012405774,0.0015416681,0.000663761,0.000105319334,0.000049863756,0.00015474045,0.000090040594,0.01282243],"genre_scores_gemma":[0.99825424,0.0003613856,0.00049712986,0.00012094574,0.000080769874,0.000007276175,0.000074119234,0.0000103552875,0.0005937721],"study_design_codex":"case_report","study_design_gemma":"case_report","domain_scores_codex":[0.99980575,0.000030187324,0.00002896676,0.00003810013,0.000031333264,0.00006571026],"domain_scores_gemma":[0.9990896,0.00038721212,0.00013761726,0.000083111954,0.00010396101,0.00019851385],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00028429859,0.0005589555,0.0003815146,0.0021556744,0.00033594118,0.0004107757,0.00066543405,0.0014838468,0.0054701716],"category_scores_gemma":[0.0018115487,0.00034067495,0.00028245602,0.000655646,0.0012864793,0.000628403,0.00040317507,0.00074203854,0.0008863068],"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":[0.00032520812,0.00009134862,0.035147954,0.000103169776,0.0000552999,0.93468374,0.0001331755,0.00034599804,0.021629851,0.0006037744,0.00082737446,0.0060529904],"study_design_scores_gemma":[0.000050240502,0.00020844495,0.0602603,0.000026904323,0.00008771279,0.9310083,0.000120416145,0.0008433741,0.0060519087,0.0004988341,0.0008178636,0.000025689376],"about_ca_topic_score_codex":0.0027822396,"about_ca_topic_score_gemma":0.0018207887,"teacher_disagreement_score":0.0054701716,"about_ca_system_score_codex":0.00035458762,"about_ca_system_score_gemma":0.00038081076,"threshold_uncertainty_score":0.01829958},"labels":[],"label_agreement":null},{"id":"W3200954735","doi":"10.1016/j.nmd.2021.07.264","title":"MOTOR NEURON DISORDERS AND NEUROPATHIES","year":2021,"lang":"en","type":"article","venue":"Neuromuscular Disorders","topic":"Hereditary Neurological Disorders","field":"Neuroscience","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":"Hospital for Sick Children","funders":"","keywords":"Medicine; Tooth disease; Epidemiology; Nerve conduction; Disease; Pathogenesis; Internal medicine; Pediatrics","score_opus":0.013517347173589987,"score_gpt":0.22123629543788118,"score_spread":0.2077189482642912,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W3200954735","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":[0.11389816,0.5247096,0.002006187,0.009085581,0.0022768334,0.00008908643,0.0017657047,0.00017935148,0.34598958],"genre_scores_gemma":[0.58970433,0.26078612,0.00340547,0.0037567338,0.0061334865,0.00009408989,0.0022064217,0.000048533428,0.1338647],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.9997348,0.000052970983,0.000031332682,0.000034278877,0.00006940073,0.000077175006],"domain_scores_gemma":[0.9997346,0.00006709704,0.000079099,0.000015877036,0.000051206855,0.000052043113],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00027027217,0.00065306795,0.00056489627,0.0018740133,0.0006013786,0.0010257635,0.00047506276,0.0009807443,0.012263469],"category_scores_gemma":[0.0008399032,0.00013475998,0.00026586044,0.0019568559,0.0008560952,0.000703845,0.0009228996,0.00060021505,0.0022955376],"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":[0.0006876149,0.00038415537,0.119396344,0.0031533274,0.00031079305,0.11372505,0.0016233549,0.00122717,0.011908202,0.14517412,0.12312769,0.47928226],"study_design_scores_gemma":[0.000053718137,0.0002023525,0.187842,0.0014517716,0.00016793236,0.21203734,0.0013050906,0.0005362491,0.0017220044,0.05873166,0.5358931,0.0000568346],"about_ca_topic_score_codex":0.0032508995,"about_ca_topic_score_gemma":0.005119195,"teacher_disagreement_score":0.012263469,"about_ca_system_score_codex":0.00046749736,"about_ca_system_score_gemma":0.0006644223,"threshold_uncertainty_score":0.0410254},"labels":[],"label_agreement":null},{"id":"W3202396661","doi":"10.1016/j.ajhg.2021.09.005","title":"ABHD16A deficiency causes a complicated form of hereditary spastic paraplegia associated with intellectual disability and cerebral anomalies","year":2021,"lang":"en","type":"article","venue":"The American Journal of Human Genetics","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":20,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Newborn Screening Ontario; McGill University Health Centre; McMaster University; McGill University; Children's Hospital of Eastern Ontario; Université Laval; University of Ottawa","funders":"National Eye Institute; National Human Genome Research Institute; National Heart, Lung, and Blood Institute; Fonds de Recherche du Québec - Santé; Genome Alberta; Ontario Genomics Institute; Genome British Columbia; Canadian Institutes of Health Research; Genome Canada; Children's Hospital of Eastern Ontario Foundation; Broad Institute; Ontario Research Foundation","keywords":"Hereditary spastic paraplegia; Spasticity; Biology; Spastic; Neuroscience; Corpus callosum; White matter; Phenotype; Allele; Genetics; Gene; Internal medicine; Medicine; Physical medicine and rehabilitation; Magnetic resonance imaging","score_opus":0.04027233370969949,"score_gpt":0.2710816134947489,"score_spread":0.23080927978504942,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W3202396661","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":[0.99644756,0.00028001732,0.0007138699,0.0001504948,0.000027928963,0.000033141707,0.00030129097,0.000054984983,0.0019907511],"genre_scores_gemma":[0.9984988,0.00011545687,0.0005305968,0.000029844321,0.000016938147,0.000008665081,0.00015535248,0.000013449259,0.0006309381],"study_design_codex":"case_report","study_design_gemma":"observational","domain_scores_codex":[0.99981564,0.000024542478,0.00003163771,0.00003696422,0.00004514212,0.000046101442],"domain_scores_gemma":[0.99949896,0.00012340325,0.0001666609,0.0000382916,0.000025769865,0.00014692493],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00013923482,0.001164727,0.00056151807,0.0009960529,0.0005336705,0.0002826443,0.00046674174,0.0007687415,0.0019575264],"category_scores_gemma":[0.00085341034,0.00036276365,0.00035994247,0.00076159684,0.00084496,0.00022065768,0.0009466137,0.0005483888,0.0003893974],"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":[0.0007287102,0.00011356453,0.043789737,0.00010401399,0.00012567271,0.8684193,0.00034131377,0.00044865298,0.07847732,0.0006985404,0.0007467765,0.0060064094],"study_design_scores_gemma":[0.0000966797,0.00039936614,0.13713115,0.000022675356,0.00009480306,0.8439635,0.0002203386,0.0015559923,0.013401805,0.00087803544,0.0021961264,0.000039467475],"about_ca_topic_score_codex":0.0025695136,"about_ca_topic_score_gemma":0.0027318697,"teacher_disagreement_score":0.0025695136,"about_ca_system_score_codex":0.00042955723,"about_ca_system_score_gemma":0.00046281883,"threshold_uncertainty_score":0.0065485835},"labels":[],"label_agreement":null},{"id":"W3204563327","doi":"10.1016/j.pediatrneurol.2021.09.011","title":"Gene-Targeted Therapies in Pediatric Neurology: Challenges and Opportunities in Diagnosis and Delivery","year":2021,"lang":"en","type":"article","venue":"Pediatric Neurology","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":19,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Hospital for Sick Children","funders":"National Institute of Neurological Disorders and Stroke","keywords":"Medicine; Neurology; Disease; Clinical trial; Intensive care medicine; Pathology; Psychiatry","score_opus":0.08300446134180756,"score_gpt":0.25200854862065114,"score_spread":0.16900408727884358,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W3204563327","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":[0.017729793,0.84943235,0.038376007,0.07673297,0.0019237946,0.00008976585,0.0002417496,0.0002277497,0.015245909],"genre_scores_gemma":[0.15913749,0.76944464,0.051717117,0.011049664,0.0037696778,0.00022221319,0.00031973078,0.00013206666,0.004207359],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.9989876,0.00040307752,0.00007424722,0.0001296366,0.00025690213,0.00014860727],"domain_scores_gemma":[0.9968791,0.002063688,0.00029866022,0.00012384843,0.00040623677,0.0002285932],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.004815487,0.00047358338,0.0013832195,0.00062405557,0.000583492,0.003337524,0.0011572548,0.0023463962,0.004216469],"category_scores_gemma":[0.0036534984,0.00027221924,0.00068182545,0.0004665004,0.002144216,0.004122108,0.0013440141,0.004303117,0.0012164147],"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":[0.0007016034,0.000500472,0.0064265835,0.0029709316,0.00013129233,0.003100972,0.00073514436,0.005002167,0.032337155,0.11923042,0.046820033,0.7820432],"study_design_scores_gemma":[0.00037883146,0.0025890989,0.00619938,0.0057157185,0.0003809,0.01631746,0.002545862,0.010218398,0.03033033,0.12543258,0.799694,0.00019738889],"about_ca_topic_score_codex":0.0018596487,"about_ca_topic_score_gemma":0.004517594,"teacher_disagreement_score":0.004815487,"about_ca_system_score_codex":0.0019451631,"about_ca_system_score_gemma":0.0027793294,"threshold_uncertainty_score":0.025467038},"labels":[],"label_agreement":null},{"id":"W3209085089","doi":"10.1016/j.prdoa.2021.100114","title":"Hereditary spastic paraplegia initially diagnosed as cerebral palsy","year":2021,"lang":"en","type":"article","venue":"Clinical Parkinsonism & Related Disorders","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":9,"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; Alberta Children's Hospital; University of Alberta","funders":"Canadian Institutes of Health Research; University of Alberta","keywords":"Medicine; Hereditary spastic paraplegia; Pediatrics; Spasticity; Family history; Spastic diplegia; Cohort; Cerebral palsy; Exome sequencing; Etiology; Spastic; Genetic testing; Physical therapy; Pathology; Internal medicine; Genetics; Biology; Mutation","score_opus":0.044313303490065056,"score_gpt":0.3241162819971529,"score_spread":0.27980297850708785,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W3209085089","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":[0.9986303,0.00015044649,0.000070783564,0.000020815134,0.0000030666913,0.000011215255,0.000107701,0.000007383769,0.0009983097],"genre_scores_gemma":[0.9991605,0.0001958783,0.0001318718,0.000041517156,0.000008122816,0.0000053934564,0.00026087448,0.000003222239,0.00019267679],"study_design_codex":"observational","study_design_gemma":"case_report","domain_scores_codex":[0.9997545,0.000020743944,0.0000156008,0.000059068818,0.00008629754,0.000063830266],"domain_scores_gemma":[0.9993825,0.000109781926,0.0002151062,0.00002598912,0.00009613587,0.00017042318],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0001622646,0.00044201995,0.00035948172,0.00086264435,0.001002108,0.0006067883,0.00033767798,0.0002821204,0.0011762393],"category_scores_gemma":[0.0012160722,0.00019942048,0.00013966417,0.00083673233,0.0005757992,0.00020539488,0.000429575,0.00032645508,0.00019231092],"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":[0.00006129953,0.000037118323,0.973153,0.00001101366,0.000014627454,0.020807544,0.0003790189,0.00005837021,0.0014725177,0.000036668112,0.0002950689,0.0036737141],"study_design_scores_gemma":[0.000008533632,0.0001338343,0.9285643,0.000021440357,0.000026373675,0.06944127,0.0005760763,0.00018804024,0.00046503963,0.000042008858,0.00052487775,0.0000082819415],"about_ca_topic_score_codex":0.04231232,"about_ca_topic_score_gemma":0.06262674,"teacher_disagreement_score":0.04231232,"about_ca_system_score_codex":0.0006043406,"about_ca_system_score_gemma":0.0010313675,"threshold_uncertainty_score":0.084132075},"labels":[],"label_agreement":null},{"id":"W3212676775","doi":"10.1093/brain/awab359","title":"Genome-wide analysis identifies impaired axonogenesis in chronic overlapping pain conditions","year":2021,"lang":"en","type":"article","venue":"Brain","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":54,"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 Clinical Research Institute; McGill University","funders":"Norwegian Institute of Public Health; Norges Forskningsråd; Medical Research Council; Helse Midt-Norge; Canada Excellence Research Chairs, Government of Canada; Fakultet for medisin og helsevitenskap, Norges Teknisk-Naturvitenskapelige Universitet; Faculty of Medicine and Health, University of Sydney; Norges Teknisk-Naturvitenskapelige Universitet","keywords":"Chronic pain; Genome; Genetics; Neuroscience; Biology; Computational biology; Medicine; Gene","score_opus":0.03345451668045335,"score_gpt":0.2707432554622455,"score_spread":0.23728873878179213,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W3212676775","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":[0.9976871,0.0005273778,0.00028083558,0.000050859515,0.0000035935107,0.0000048676893,0.0011686187,0.000008574052,0.00026813953],"genre_scores_gemma":[0.99820054,0.00028680134,0.00033890165,0.000030873947,0.0000047894155,0.000006539322,0.0009863852,0.000005384217,0.00013984286],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9996213,0.00007615363,0.00003277295,0.00016753776,0.000051190895,0.00005102868],"domain_scores_gemma":[0.999257,0.00024680764,0.00032340403,0.000049402683,0.00004509432,0.00007815987],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0003397548,0.00029968348,0.00036798717,0.0011357404,0.00031106925,0.00050773914,0.00025888314,0.0005703562,0.0022958727],"category_scores_gemma":[0.0010655486,0.00016061994,0.00039461852,0.0012924211,0.0003544502,0.00013712261,0.0005393038,0.0003506722,0.00013877766],"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":[0.0017423945,0.000070955815,0.9309284,0.00019103065,0.0012458188,0.002466813,0.00033496018,0.0005382725,0.04917333,0.0002699107,0.00091743865,0.012120711],"study_design_scores_gemma":[0.000011102704,0.00003128982,0.99821585,0.00000963247,0.000107346386,0.00070961885,0.000049733913,0.00015475212,0.0004201499,0.00006026211,0.00022642614,0.0000037900404],"about_ca_topic_score_codex":0.005984033,"about_ca_topic_score_gemma":0.00853122,"teacher_disagreement_score":0.005984033,"about_ca_system_score_codex":0.00020618505,"about_ca_system_score_gemma":0.00016417858,"threshold_uncertainty_score":0.011898398},"labels":[],"label_agreement":null},{"id":"W3214997848","doi":"10.1002/ana.26275","title":"Heterozygous De Novo <scp><i>KPNA3</i></scp> Mutations Cause Complex Hereditary Spastic Paraplegia","year":2021,"lang":"en","type":"letter","venue":"Annals of Neurology","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":1,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Ottawa; Montreal Neurological Institute and Hospital; SickKids Foundation; University of Toronto; Children's Hospital of Eastern Ontario; McGill University; Hospital for Sick Children","funders":"Canadian Institutes of Health Research","keywords":"Sick child; Medicine; Annals; Hereditary spastic paraplegia; University hospital; Gerontology; Family medicine; Pediatrics; Library science; History; Biology","score_opus":0.1746705584682186,"score_gpt":0.3308486661186753,"score_spread":0.1561781076504567,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W3214997848","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":[0.093701,0.005476286,0.0016875799,0.7307738,0.0403353,0.00018642069,0.001001745,0.0004623327,0.12637556],"genre_scores_gemma":[0.55029005,0.0054202853,0.002624518,0.28517398,0.09930611,0.00014465187,0.0005335997,0.00030129112,0.05620552],"study_design_codex":"case_report","study_design_gemma":"observational","domain_scores_codex":[0.99948186,0.00007661027,0.00007340298,0.00008575754,0.00012420838,0.00015826461],"domain_scores_gemma":[0.9980388,0.0009225116,0.00021234245,0.00009104594,0.00031440504,0.0004208284],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0005221442,0.0014379689,0.001140753,0.0010042622,0.0024768207,0.0015210869,0.001339803,0.018784212,0.0059152846],"category_scores_gemma":[0.005483153,0.000501569,0.0011760925,0.00083721115,0.0015257748,0.001237401,0.0006871033,0.007460629,0.0032988754],"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":[0.00014388878,0.00007782364,0.005205192,0.00008276291,0.000052752,0.8235619,0.00016363461,0.00026010151,0.0012491645,0.002159941,0.16089945,0.0061434596],"study_design_scores_gemma":[0.00033621033,0.00018722474,0.01190027,0.00028553428,0.00018367093,0.86018044,0.00044528386,0.0034281437,0.0021456613,0.009288157,0.111526184,0.00009319909],"about_ca_topic_score_codex":0.0060348953,"about_ca_topic_score_gemma":0.0060624965,"teacher_disagreement_score":0.018784212,"about_ca_system_score_codex":0.0026672792,"about_ca_system_score_gemma":0.0013692975,"threshold_uncertainty_score":0.019788623},"labels":[],"label_agreement":null},{"id":"W3217386291","doi":"10.1111/jns.12477","title":"A longitudinal and cross‐sectional study of plasma neurofilament light chain concentration in <scp>Charcot‐Marie‐Tooth</scp> disease","year":2021,"lang":"en","type":"article","venue":"Journal of the Peripheral Nervous System","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":35,"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":"H2020 European Research Council; Wellcome Trust; National Center for Advancing Translational Sciences; National Institute of Neurological Disorders and Stroke; Medical Research Council; International Nut and Dried Fruit Council; Medical Research Council Canada; Vetenskapsrådet; Alzheimer's Drug Discovery Foundation; British Medical Association; Muscular Dystrophy Association; Charcot-Marie-Tooth Association","keywords":"Cohort; Biomarker; Medicine; Internal medicine; Disease; Cohort study; Cross-sectional study; Oncology; Gastroenterology; Pathology; Biology; Genetics","score_opus":0.026393445299755607,"score_gpt":0.25771860194439655,"score_spread":0.23132515664464096,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W3217386291","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":[0.99910295,0.00015625458,0.00016543957,0.000020658628,0.0000038764397,0.000008055499,0.00028504408,0.000007654074,0.00025016654],"genre_scores_gemma":[0.9988065,0.000060438128,0.0001633628,0.000033384487,0.000005799087,0.0000142679355,0.0004564736,0.0000038719136,0.00045592542],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.999716,0.000067900946,0.000021093127,0.000108734836,0.00004938994,0.000036919777],"domain_scores_gemma":[0.9989987,0.00012372698,0.00039531663,0.00006453834,0.00017437138,0.00024345925],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00067233044,0.00023563496,0.00024178774,0.00046209805,0.00036806907,0.0004259323,0.00014545812,0.00047600784,0.0010545047],"category_scores_gemma":[0.00080753514,0.00020535456,0.00025419105,0.00033641278,0.00017074298,0.00033465485,0.00023893184,0.00061017286,0.0002962394],"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":[0.0026543809,0.00035020738,0.9540361,0.000028369626,0.00022732688,0.00048738494,0.00020832656,0.000102941245,0.037342057,0.00004388747,0.0003353801,0.004183545],"study_design_scores_gemma":[0.000012793214,0.00078670494,0.9970739,0.000003719471,0.00003594408,0.0006428055,0.00006337351,0.00014038161,0.00094650517,0.000015469237,0.0002734728,0.0000049687037],"about_ca_topic_score_codex":0.0020164435,"about_ca_topic_score_gemma":0.0017148359,"teacher_disagreement_score":0.0020164435,"about_ca_system_score_codex":0.00026584146,"about_ca_system_score_gemma":0.00012798903,"threshold_uncertainty_score":0.004009366},"labels":[],"label_agreement":null},{"id":"W4200198138","doi":"10.3233/jnd-210716","title":"Homozygous N-terminal missense variant in PLEKHG5 associated with intermediate CMT: A case report","year":2021,"lang":"en","type":"article","venue":"Journal of Neuromuscular Diseases","topic":"Hereditary Neurological Disorders","field":"Neuroscience","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":"Ottawa Hospital; Children's Hospital of Eastern Ontario; University of Ottawa","funders":"","keywords":"Missense mutation; Genetics; Exome sequencing; Phenotype; Pleckstrin homology domain; Zinc finger; Mutation; RHOA; Medicine; Biology; Gene; Signal transduction","score_opus":0.022800950693110455,"score_gpt":0.2581670848435923,"score_spread":0.23536613415048185,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4200198138","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":[0.99216425,0.0010676621,0.0019316663,0.00075146847,0.00010920781,0.00007335208,0.0001882854,0.00012478812,0.003589291],"genre_scores_gemma":[0.997563,0.00031459518,0.0007127373,0.00018882599,0.00020647266,0.000015066634,0.00007919507,0.000016084392,0.00090418436],"study_design_codex":"case_report","study_design_gemma":"case_report","domain_scores_codex":[0.9994381,0.000038777016,0.00005533466,0.00021085342,0.00008486634,0.00017211703],"domain_scores_gemma":[0.9988085,0.0003140866,0.00021037504,0.00012242254,0.000064266205,0.00048033526],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00030457933,0.0020919822,0.001384291,0.0020859505,0.0023447615,0.0016525176,0.0012427766,0.0042994795,0.0029810725],"category_scores_gemma":[0.0017006432,0.0012354825,0.0011801876,0.0011746011,0.0022288456,0.0012137486,0.0017801463,0.0020712565,0.00096140156],"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":[0.000028615246,0.000030962008,0.002822845,0.000015903865,0.000011737583,0.99521446,0.00012447406,0.00003441186,0.0010487806,0.00008789405,0.00010875307,0.00047115888],"study_design_scores_gemma":[0.000009663877,0.000038578975,0.00331179,0.0000047504186,0.000015075981,0.9958456,0.000050647166,0.00012342918,0.00037950726,0.00006699825,0.00014528373,0.000008676939],"about_ca_topic_score_codex":0.0019321762,"about_ca_topic_score_gemma":0.001898339,"teacher_disagreement_score":0.0042994795,"about_ca_system_score_codex":0.0010276595,"about_ca_system_score_gemma":0.00054255896,"threshold_uncertainty_score":0.009972632},"labels":[],"label_agreement":null},{"id":"W4205250191","doi":"10.3917/cerpsy.074.0026","title":"Comment bien nourrir ses neurones","year":2016,"lang":"fr","type":"article","venue":"Cerveau & Psycho","topic":"Hereditary Neurological Disorders","field":"Neuroscience","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":"World Federation of Science Journalists","funders":"","keywords":"Neuroscience; Psychology","score_opus":0.053173975913230524,"score_gpt":0.299568421272469,"score_spread":0.2463944453592385,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4205250191","genre_codex":"commentary","genre_gemma":"commentary","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"commentary","genre_consensus":"commentary","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.0013105156,0.008104475,0.00015858137,0.9146096,0.07144435,0.000006537375,0.00006602855,0.00006139554,0.004238485],"genre_scores_gemma":[0.014156209,0.0053388425,0.00026489986,0.8703665,0.07939851,0.000034006694,0.000062051426,0.00003991978,0.030339051],"study_design_codex":"not_applicable","study_design_gemma":"not_applicable","domain_scores_codex":[0.99794096,0.0003651233,0.00029333317,0.00042936477,0.0006899648,0.00028116864],"domain_scores_gemma":[0.993075,0.0034974925,0.00074395,0.0003350817,0.0018232071,0.0005253095],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0018534501,0.000606293,0.00103321,0.00042402174,0.0023458,0.0018658397,0.0017877462,0.022897277,0.012037112],"category_scores_gemma":[0.023979863,0.00036228547,0.0011079198,0.0004051918,0.0026455843,0.003213833,0.0013846918,0.020419788,0.011836255],"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":[0.00018795601,0.0000315726,0.0012884311,0.00031580083,0.000052309704,0.004733657,0.0005318523,0.00010118167,0.0009277217,0.0054594534,0.969301,0.017069157],"study_design_scores_gemma":[0.000081406295,0.00007175569,0.00294522,0.00042617173,0.00005683265,0.009396251,0.000926009,0.00011217036,0.00078378996,0.0051953983,0.97993535,0.000069681715],"about_ca_topic_score_codex":0.010289209,"about_ca_topic_score_gemma":0.0149511015,"teacher_disagreement_score":0.022897277,"about_ca_system_score_codex":0.0019911523,"about_ca_system_score_gemma":0.0019296436,"threshold_uncertainty_score":0.040268123},"labels":[],"label_agreement":null},{"id":"W4206261479","doi":"10.1016/j.nmd.2021.07.379","title":"OTHER NMDs","year":2021,"lang":"en","type":"article","venue":"Neuromuscular Disorders","topic":"Hereditary Neurological Disorders","field":"Neuroscience","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":"Hospital for Sick Children","funders":"","keywords":"Epidemiology; Medicine; Incidence (geometry); Mendelian inheritance; Disease; Genotype; Molecular epidemiology; Demography; Genetics; Biology; Internal medicine; Gene","score_opus":0.024546814383274208,"score_gpt":0.24780000776657213,"score_spread":0.2232531933832979,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4206261479","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":[0.10655157,0.062566064,0.002946088,0.004086862,0.0030906538,0.00032831385,0.009478787,0.000815565,0.81013614],"genre_scores_gemma":[0.59486395,0.0341261,0.003138414,0.0091204755,0.0025091167,0.00033787222,0.02082911,0.00030115957,0.33477378],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.99978393,0.000017273882,0.000019864508,0.000044993187,0.000057391564,0.0000764701],"domain_scores_gemma":[0.9996933,0.00005202553,0.000052413478,0.000032908018,0.00005825155,0.00011105471],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00017562881,0.0005829586,0.0006034965,0.00093010516,0.0010105795,0.00053859694,0.00038093422,0.0006923784,0.062144436],"category_scores_gemma":[0.00068924035,0.00006565326,0.00077828654,0.0008166093,0.00023384913,0.00031269868,0.0005479768,0.00084278086,0.018276911],"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":[0.0014571872,0.0008831294,0.095512316,0.0029892828,0.00060556823,0.048657894,0.00034930842,0.00038904158,0.012534999,0.008025235,0.24806114,0.58053476],"study_design_scores_gemma":[0.00023164484,0.0004917221,0.07849283,0.001373425,0.0003800437,0.08053717,0.00023361422,0.00029404255,0.0028623326,0.0025870628,0.8324762,0.000039928433],"about_ca_topic_score_codex":0.0026002887,"about_ca_topic_score_gemma":0.0056256964,"teacher_disagreement_score":0.062144436,"about_ca_system_score_codex":0.00048562844,"about_ca_system_score_gemma":0.0007491987,"threshold_uncertainty_score":0},"labels":[],"label_agreement":null},{"id":"W4210875960","doi":"10.1093/brain/awac055","title":"NCAM1 and GDF15 are biomarkers of Charcot-Marie-Tooth disease in patients and mice","year":2022,"lang":"en","type":"article","venue":"Brain","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":37,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Jewish General Hospital; McGill University; Ottawa Hospital; Children's Hospital of Eastern Ontario; University of Ottawa","funders":"European Regional Development Fund; National Institutes of Health; Wellcome Trust; Ministry of Science and Higher Education of the Russian Federation; Vlaamse regering; NIHR Cambridge Biomedical Research Centre; Skolkovo Institute of Science and Technology; Lily Foundation; Evelyn Trust; Warren Y. Soper Charitable Trust; Universiteit Antwerpen; Fondation Médicale Reine Elisabeth; Canada Research Chairs; Medical Research Council; Department of Health and Social Care; Ataxia UK; McGill University; Muscular Dystrophy Canada; Canadian Institutes of Health Research; Fonds Wetenschappelijk Onderzoek; Jewish General Hospital; Muscular Dystrophy Association; Association Belge contre les Maladies Neuro-Musculaires; Canada Foundation for Innovation; Newton Fund; Fondation De Famille Alvin Segal; National Institute for Health and Care Research; Stoneygate Trust; Genome Canada; National Institute of Neurological Disorders and Stroke; Charcot-Marie-Tooth Association","keywords":"Neural cell adhesion molecule; Biomarker; Medicine; Disease; Cell; Bioinformatics; Internal medicine; Biology; Cell adhesion; Genetics","score_opus":0.015579312629909923,"score_gpt":0.22106741235691352,"score_spread":0.2054880997270036,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4210875960","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":[0.99266654,0.002328725,0.0028897056,0.00017274855,0.00003512553,0.000051104762,0.0010994341,0.0001251561,0.0006313838],"genre_scores_gemma":[0.9932208,0.0007419226,0.0037943202,0.00025588134,0.000017489236,0.00009978927,0.0012080523,0.000023210741,0.0006385378],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9992173,0.0001152426,0.00011143054,0.000278606,0.00019704209,0.00008051094],"domain_scores_gemma":[0.9995171,0.00006848522,0.00024033847,0.00004775211,0.000049763512,0.000076503595],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00072579074,0.0006712855,0.0004080577,0.0012694709,0.00025764114,0.0004748292,0.00024230237,0.0007939046,0.00071530504],"category_scores_gemma":[0.00063690403,0.00023602573,0.00033332867,0.00057967193,0.00041368505,0.0002903601,0.0003859151,0.00063002185,0.00018516676],"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":[0.0012622285,0.00010856829,0.09178618,0.00017504605,0.00015963757,0.00068481883,0.00009591312,0.000120923134,0.8978939,0.00010187712,0.00029221,0.007318715],"study_design_scores_gemma":[0.00007490375,0.0017168344,0.723246,0.00008629809,0.0002581252,0.008260617,0.00021770697,0.0014252412,0.25958884,0.0004527604,0.0046410635,0.000031626656],"about_ca_topic_score_codex":0.00042230153,"about_ca_topic_score_gemma":0.00090383383,"teacher_disagreement_score":0.0012694709,"about_ca_system_score_codex":0.00025993874,"about_ca_system_score_gemma":0.00016068795,"threshold_uncertainty_score":0.00383842},"labels":[],"label_agreement":null},{"id":"W4210891645","doi":"10.1136/jnnp-2021-328483","title":"Clinical practice guideline for the management of paediatric Charcot-Marie-Tooth disease","year":2022,"lang":"en","type":"review","venue":"Journal of Neurology Neurosurgery & Psychiatry","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":43,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"McMaster University","funders":"National Institute of Neurological Disorders and Stroke","keywords":"Guideline; Medicine; Multidisciplinary approach; Delphi method; Clinical Practice; Grading (engineering); Health care; Disease management; Evidence-based medicine; Best practice; MEDLINE; Intensive care medicine; Physical therapy; Alternative medicine; Health management system; Pathology","score_opus":0.10508457850666571,"score_gpt":0.4012642693524687,"score_spread":0.29617969084580303,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4210891645","genre_codex":"commentary","genre_gemma":"review","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"review","genre_consensus":null,"domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.004913303,0.1982965,0.07863107,0.45251495,0.03895057,0.033559337,0.018872218,0.0019991815,0.17226297],"genre_scores_gemma":[0.026447037,0.17651793,0.58620983,0.100821316,0.005621359,0.033898626,0.031210912,0.00041064268,0.0388624],"study_design_codex":"not_applicable","study_design_gemma":"not_applicable","domain_scores_codex":[0.97122383,0.011871248,0.007914206,0.0010360202,0.00692143,0.0010332757],"domain_scores_gemma":[0.94609064,0.015587153,0.005473281,0.0010250052,0.029516373,0.002307636],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0129350275,0.0018805016,0.0028477437,0.0073175877,0.0018514672,0.0036688554,0.0067594475,0.01354823,0.010740866],"category_scores_gemma":[0.06304037,0.0011653717,0.005548851,0.005772611,0.0015759593,0.0032735346,0.0031904958,0.010489953,0.009050524],"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":[0.000078872705,0.00019986361,0.0010279535,0.01764358,0.0002472726,0.0011754783,0.0010159959,0.0012687456,0.00064368185,0.006431616,0.76960886,0.20065807],"study_design_scores_gemma":[0.00046757635,0.00014900706,0.003711,0.087741375,0.00068806455,0.0021623399,0.0004832541,0.0011640834,0.00043055232,0.008365576,0.89450175,0.00013537687],"about_ca_topic_score_codex":0.02426739,"about_ca_topic_score_gemma":0.046232685,"teacher_disagreement_score":0.02426739,"about_ca_system_score_codex":0.0075632622,"about_ca_system_score_gemma":0.032667603,"threshold_uncertainty_score":0.068407774},"labels":[],"label_agreement":null},{"id":"W4214718780","doi":"10.1093/hmg/ddac053","title":"De novo variants in <i>EMC1</i> lead to neurodevelopmental delay and cerebellar degeneration and affect glial function in <i>Drosophila</i>","year":2022,"lang":"en","type":"article","venue":"Human Molecular Genetics","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":17,"is_retracted":false,"has_abstract":true,"route_ca_aff":false,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"","funders":"Eunice Kennedy Shriver National Institute of Child Health and Human Development; National Institute of Neurological Disorders and Stroke; National Human Genome Research Institute; National Heart, Lung, and Blood Institute; Canadian Institutes of Health Research; Baylor-Hopkins Center for Mendelian Genomics; National Institutes of Health; Warren Alpert Foundation","keywords":"Biology; Exome sequencing; Genetics; Phenotype; Gene knockdown; Loss function; Allele; Exome; Compound heterozygosity; Gene","score_opus":0.021509072284122868,"score_gpt":0.2449998193068423,"score_spread":0.22349074702271943,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4214718780","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":[0.9922693,0.0004139639,0.0036234392,0.000104922205,0.000023886332,0.00005891583,0.0014555063,0.00019155857,0.0018585575],"genre_scores_gemma":[0.99119484,0.00043357068,0.0044518365,0.00012620995,0.000014519689,0.000038076123,0.0014340358,0.000102077014,0.0022047427],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99986494,0.000012925292,0.000019359504,0.000056772664,0.000030108604,0.000015867572],"domain_scores_gemma":[0.9998196,0.00003920337,0.000073782896,0.000017359183,0.000015133211,0.000034943896],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00011469448,0.0007823846,0.00021817508,0.00041280675,0.00029844776,0.00022720687,0.0002857159,0.0005356866,0.0019157531],"category_scores_gemma":[0.00017335246,0.00013464336,0.00029619646,0.00019330843,0.0003212622,0.00012467703,0.00029824182,0.00060692284,0.0003892495],"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":[0.00012565852,0.00005417758,0.0037026005,0.00007282711,0.00004455727,0.003412575,0.00005343095,0.0002441331,0.9883306,0.00025053203,0.00025449359,0.0034544384],"study_design_scores_gemma":[0.00007009395,0.0004756657,0.11620196,0.00005115761,0.0002284442,0.02856637,0.00014582719,0.0034026229,0.8411805,0.00021650127,0.0094232485,0.00003758828],"about_ca_topic_score_codex":0.0014621677,"about_ca_topic_score_gemma":0.0037961123,"teacher_disagreement_score":0.0019157531,"about_ca_system_score_codex":0.00041397894,"about_ca_system_score_gemma":0.00018196485,"threshold_uncertainty_score":0.0064088106},"labels":[],"label_agreement":null},{"id":"W4220708625","doi":"10.1186/s12883-022-02595-4","title":"An integrated modelling methodology for estimating global incidence and prevalence of hereditary spastic paraplegia subtypes SPG4, SPG7, SPG11, and SPG15","year":2022,"lang":"en","type":"article","venue":"BMC Neurology","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":22,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"SickKids Foundation; Hospital for Sick Children; University of Toronto","funders":"Agence Nationale de la Recherche","keywords":"Epidemiology; Medicine; Incidence (geometry); Genetic epidemiology; Hereditary spastic paraplegia; Mendelian inheritance; Pedigree chart; Disease; Public health; Molecular epidemiology; Genetics; Demography; Genotype; Pathology; Biology; Gene","score_opus":0.11555893587614668,"score_gpt":0.33360180000976614,"score_spread":0.21804286413361945,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4220708625","genre_codex":"methods","genre_gemma":"methods","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"methods","genre_consensus":"methods","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.041149467,0.00033398985,0.9543317,0.0003207798,0.000042650685,0.00020008806,0.0012568389,0.00031406188,0.0020503728],"genre_scores_gemma":[0.59499335,0.00090856856,0.39711192,0.0001616895,0.00007786091,0.001287943,0.0030308703,0.00012051733,0.0023072427],"study_design_codex":"simulation_or_modeling","study_design_gemma":"simulation_or_modeling","domain_scores_codex":[0.9975038,0.0014990498,0.0001629692,0.000437727,0.0002392565,0.0001571546],"domain_scores_gemma":[0.99123704,0.006597868,0.0008473636,0.00037986197,0.0008193005,0.000118484226],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0071200365,0.0011421879,0.0011967248,0.0029917008,0.0005093784,0.0019991077,0.0020556757,0.0016115124,0.0030262233],"category_scores_gemma":[0.019783799,0.000723699,0.0030585506,0.0027545858,0.0005634326,0.0011528274,0.001749896,0.0014393535,0.0005038425],"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":[0.000048317765,0.000051684565,0.013496851,0.000112529815,0.00028961644,0.00010876495,0.00014703385,0.95285946,0.00033842723,0.011034362,0.00066575926,0.020847209],"study_design_scores_gemma":[0.0000122241645,0.00004794172,0.0014825417,0.0000373069,0.00007434124,0.00006563638,0.00005037967,0.9899664,0.00011672965,0.0071926885,0.0009389331,0.000014825882],"about_ca_topic_score_codex":0.021625474,"about_ca_topic_score_gemma":0.012504064,"teacher_disagreement_score":0.021625474,"about_ca_system_score_codex":0.0017751524,"about_ca_system_score_gemma":0.0025783596,"threshold_uncertainty_score":0.04299915},"labels":[],"label_agreement":null},{"id":"W4220715780","doi":"10.1002/mgg3.1927","title":"A novel <i>UBAP1</i> truncated variant in a Chinese family with hereditary spastic paraplegia","year":2022,"lang":"en","type":"letter","venue":"Molecular Genetics & Genomic Medicine","topic":"Hereditary Neurological Disorders","field":"Neuroscience","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":"Hereditary spastic paraplegia; Proband; Medicine; Weakness; Spasticity; Spinal muscular atrophy; Pediatrics; Genetics; Physical therapy; Internal medicine; Disease; Phenotype; Anatomy; Biology; Gene; Mutation","score_opus":0.022136403839745286,"score_gpt":0.23390048243931252,"score_spread":0.21176407859956725,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4220715780","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":[0.99727976,0.0004380734,0.0006242826,0.00029826126,0.000057906178,0.000040874715,0.00013224666,0.000038853574,0.001089758],"genre_scores_gemma":[0.99847144,0.0001753152,0.00033581883,0.00017959306,0.000055023258,0.000009188891,0.000073476825,0.0000084365765,0.0006917056],"study_design_codex":"case_report","study_design_gemma":"case_report","domain_scores_codex":[0.99973303,0.000018783203,0.000037487156,0.000113673304,0.00004085033,0.00005608442],"domain_scores_gemma":[0.99957305,0.000086915075,0.00010041619,0.000028493936,0.00003595793,0.00017504362],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0002515134,0.0011360866,0.0007785837,0.0010897311,0.001842071,0.00038831925,0.0008166785,0.0011151519,0.001981224],"category_scores_gemma":[0.00060488953,0.0004072787,0.00083334104,0.0011054819,0.0010965656,0.00037150175,0.000596245,0.0007046007,0.00037087736],"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":[0.00013533124,0.00006613721,0.025146896,0.000074673604,0.000046842517,0.9518911,0.00126296,0.00017191388,0.01716909,0.0003073181,0.00045436,0.0032733534],"study_design_scores_gemma":[0.00006676094,0.0004415818,0.1604436,0.000051993673,0.00020865156,0.8286126,0.00053514296,0.0011292399,0.005385191,0.00042911049,0.0026173012,0.000078733945],"about_ca_topic_score_codex":0.010614807,"about_ca_topic_score_gemma":0.009676986,"teacher_disagreement_score":0.010614807,"about_ca_system_score_codex":0.00071686064,"about_ca_system_score_gemma":0.0006647681,"threshold_uncertainty_score":0.021106064},"labels":[],"label_agreement":null},{"id":"W4221093737","doi":"10.1002/mdc3.13437","title":"Spastic Paraplegia Type 7 and Movement Disorders: Beyond the Spastic Paraplegia","year":2022,"lang":"en","type":"article","venue":"Movement Disorders Clinical Practice","topic":"Hereditary Neurological Disorders","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":"Ontario Brain Institute; Toronto Western Hospital; University of Toronto","funders":"","keywords":"Hereditary spastic paraplegia; Dystonia; Parkinsonism; Movement disorders; Paraplegia; Spastic; Medicine; Ataxia; Cerebellar ataxia; Physical medicine and rehabilitation; Phenotype; Pediatrics; Internal medicine; Genetics; Psychiatry; Cerebral palsy; Biology; Gene; Spinal cord","score_opus":0.05297497224385309,"score_gpt":0.34570599844030836,"score_spread":0.29273102619645525,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4221093737","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":[0.98923737,0.003403738,0.00058205606,0.0003850202,0.00004727285,0.000027125137,0.00018033525,0.000027732824,0.0061094374],"genre_scores_gemma":[0.9965139,0.0013793223,0.0005875151,0.000174974,0.00015009959,0.0000125887245,0.00022663627,0.0000110253895,0.00094394956],"study_design_codex":"observational","study_design_gemma":"not_applicable","domain_scores_codex":[0.9997507,0.00004597398,0.000044943572,0.000043875792,0.000063126514,0.000051379866],"domain_scores_gemma":[0.99940324,0.00016713244,0.00018760138,0.000041745432,0.0000790329,0.00012121101],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00031159015,0.0006391186,0.0004685893,0.0010029065,0.00047174466,0.0003874754,0.00032123097,0.0004989773,0.0052491818],"category_scores_gemma":[0.0009864066,0.00016047113,0.00024153544,0.00076610106,0.0005510172,0.00043976784,0.000573729,0.00039861508,0.00090741046],"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":[0.00034751443,0.00010678488,0.74743646,0.00023938499,0.00009125193,0.20460606,0.00062095234,0.0001293362,0.009855689,0.00038774876,0.0017846286,0.034394305],"study_design_scores_gemma":[0.000022336511,0.00019574896,0.32124943,0.00013206442,0.00008110703,0.6719267,0.00039943948,0.00020937446,0.0017143027,0.00054512464,0.0035112633,0.000013139602],"about_ca_topic_score_codex":0.0012890692,"about_ca_topic_score_gemma":0.0023535094,"teacher_disagreement_score":0.0052491818,"about_ca_system_score_codex":0.00022145588,"about_ca_system_score_gemma":0.0004930367,"threshold_uncertainty_score":0.017560244},"labels":[],"label_agreement":null},{"id":"W4224060853","doi":"10.1111/jns.12492","title":"Unusual upper limb features in <i>SORD</i> neuropathy","year":2022,"lang":"en","type":"letter","venue":"Journal of the Peripheral Nervous System","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":8,"is_retracted":false,"has_abstract":false,"route_ca_aff":false,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"","funders":"Medical Research Council; European Academy of Neurology; Medical Research Council Canada; Fondazione Cariplo; Rare Diseases Clinical Research Network; National Institute for Health and Care Research; Muscular Dystrophy Association","keywords":"Queen (butterfly); Neurology; Neurosurgery; Square (algebra); Medicine; Surgery; Psychiatry","score_opus":0.01703866315540358,"score_gpt":0.22644805747408778,"score_spread":0.2094093943186842,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4224060853","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":[0.62998724,0.006828296,0.0065583247,0.07596426,0.007014529,0.0006025266,0.0013507745,0.0011882383,0.2705058],"genre_scores_gemma":[0.96614486,0.0015372159,0.002737283,0.010747407,0.009202981,0.00009266563,0.0002480963,0.00010679122,0.009182681],"study_design_codex":"case_report","study_design_gemma":"case_report","domain_scores_codex":[0.9992053,0.00011229362,0.00008753655,0.00016194001,0.00013592208,0.00029704595],"domain_scores_gemma":[0.997241,0.0012374361,0.0003532742,0.00023280067,0.00029928653,0.0006360652],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0007239987,0.0027992507,0.0015113192,0.0024426198,0.0022462148,0.002120184,0.0023404341,0.009906755,0.004752612],"category_scores_gemma":[0.0051543685,0.0007087637,0.0013456405,0.001636631,0.0022248693,0.002068971,0.0012019651,0.004691894,0.0013701551],"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":[0.00003117962,0.000018193035,0.0013545974,0.000026724261,0.0000047495496,0.9955173,0.00003391514,0.00007380058,0.00024301722,0.00035262704,0.0016995011,0.00064434134],"study_design_scores_gemma":[0.00003297379,0.00006936481,0.006323959,0.000049395967,0.00001937202,0.98959374,0.00009686112,0.00072474545,0.00026989105,0.0009920963,0.0018087758,0.00001886192],"about_ca_topic_score_codex":0.0040537487,"about_ca_topic_score_gemma":0.0050055203,"teacher_disagreement_score":0.009906755,"about_ca_system_score_codex":0.0024060728,"about_ca_system_score_gemma":0.0009938419,"threshold_uncertainty_score":0.017457366},"labels":[],"label_agreement":null},{"id":"W4224945122","doi":"10.1002/ana.26381","title":"Biallelic Variants in the Ectonucleotidase <scp><i>ENTPD1</i></scp> Cause a Complex Neurodevelopmental Disorder with Intellectual Disability, Distinct White Matter Abnormalities, and Spastic Paraplegia","year":2022,"lang":"en","type":"article","venue":"Annals of Neurology","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":9,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Newborn Screening Ontario; Children's Hospital of Eastern Ontario; Dalhousie University; University of Ottawa","funders":"National Institute of Neurological Disorders and Stroke; National Human Genome Research Institute; Canadian Institutes of Health Research; American Brain Foundation; Erasmus Universitair Medisch Centrum Rotterdam; Conselho Nacional de Desenvolvimento Científico e Tecnológico; International Rett Syndrome Foundation; Medical Research Council; Spastic Paraplegia Foundation; National Institutes of Health; Brain and Behavior Research Foundation; Ontario Genomics; U.S. Department of Defense; Brain Research UK; Genome Canada; Cerebral Palsy Alliance Research Foundation; Cerebral Palsy Alliance; Genome British Columbia; National Institute of General Medical Sciences; Ontario Genomics Institute; Muscular Dystrophy Association; Uehara Memorial Foundation; Baylor-Hopkins Center for Mendelian Genomics; Genome Alberta; Johns Hopkins University; European Commission","keywords":"Genetics; Hereditary spastic paraplegia; Intellectual disability; Spastic; Locus (genetics); Biology; Neurodevelopmental disorder; White matter; Medicine; Phenotype; Gene; Cerebral palsy; Psychiatry","score_opus":0.07482103277295621,"score_gpt":0.27987416325987985,"score_spread":0.20505313048692364,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4224945122","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":[0.99636203,0.00038609572,0.0008264901,0.00008568673,0.000008686995,0.0000356264,0.0009719394,0.000039312486,0.0012841781],"genre_scores_gemma":[0.99715316,0.00018790302,0.000643136,0.00007189391,0.000018578625,0.000017412585,0.00067756494,0.000016919772,0.001213601],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9997631,0.000015294416,0.000028717044,0.00011406288,0.00005028677,0.000028549162],"domain_scores_gemma":[0.99978036,0.000034074183,0.00010353316,0.000010566971,0.000021850403,0.000049624854],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00012086854,0.0009835355,0.0003475149,0.00061746157,0.00061257975,0.00031461878,0.00026719377,0.0004107015,0.0040588905],"category_scores_gemma":[0.00036302969,0.00016625108,0.00021345197,0.0007123428,0.00034253535,0.00014481723,0.00052986393,0.0003342203,0.00080209196],"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":[0.0015298591,0.000256955,0.48098162,0.0002144353,0.0004328392,0.0848233,0.0010835009,0.00032562984,0.39888105,0.00043854406,0.0023529963,0.028679242],"study_design_scores_gemma":[0.00008583785,0.00047225002,0.81539977,0.000047282614,0.00025589133,0.14623173,0.00038727952,0.00055495417,0.030393729,0.00026109762,0.00588208,0.00002811498],"about_ca_topic_score_codex":0.0019059851,"about_ca_topic_score_gemma":0.002762924,"teacher_disagreement_score":0.0040588905,"about_ca_system_score_codex":0.00023998068,"about_ca_system_score_gemma":0.00021523982,"threshold_uncertainty_score":0.013578355},"labels":[],"label_agreement":null},{"id":"W4225163181","doi":"10.53738/revmed.2022.18.779.803","title":"Diagnostiquer une neuropathie des petites fibres","year":2022,"lang":"fr","type":"article","venue":"Revue Médicale Suisse","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":false,"ca_institutions":"Hotel Dieu Hospital","funders":"","keywords":"Medicine; Etiology; Gynecology; Skin biopsy; Dermatology; Biopsy; Pathology","score_opus":0.034794433179974806,"score_gpt":0.25877955790964297,"score_spread":0.22398512472966817,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4225163181","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":[0.84156793,0.034650102,0.0422053,0.014517572,0.0017617589,0.00048789562,0.0006120134,0.0017598809,0.06243746],"genre_scores_gemma":[0.94891524,0.009700918,0.018885072,0.0023632182,0.001628521,0.00013288755,0.0003922367,0.00012987756,0.017852155],"study_design_codex":"case_report","study_design_gemma":"not_applicable","domain_scores_codex":[0.99881554,0.00015759162,0.000086983404,0.00034585784,0.00038612512,0.0002079202],"domain_scores_gemma":[0.99795365,0.00109765,0.00030465086,0.00011489145,0.00032064662,0.00020853835],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0009165909,0.0019311071,0.0013973761,0.0018427041,0.0017340834,0.0025709402,0.00093274884,0.004535158,0.0061213393],"category_scores_gemma":[0.0058417055,0.0008206118,0.0011511293,0.00076361716,0.0018255041,0.0025719982,0.000811864,0.005239411,0.0018630861],"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":[0.00061275176,0.00058442925,0.05751802,0.0010451338,0.0003062469,0.7483121,0.002199665,0.003094006,0.04748967,0.007142827,0.0058835726,0.12581153],"study_design_scores_gemma":[0.000121114426,0.0005755989,0.057166833,0.00049170025,0.00009523812,0.8977873,0.0005959335,0.0037362145,0.01739404,0.0015980802,0.020345712,0.000092348106],"about_ca_topic_score_codex":0.010941682,"about_ca_topic_score_gemma":0.008292159,"teacher_disagreement_score":0.010941682,"about_ca_system_score_codex":0.0014568251,"about_ca_system_score_gemma":0.0007473276,"threshold_uncertainty_score":0.021755993},"labels":[],"label_agreement":null},{"id":"W4225252429","doi":"10.1016/j.parkreldis.2022.03.019","title":"Genetic, structural and clinical analysis of spastic paraplegia 4","year":2022,"lang":"en","type":"article","venue":"Parkinsonism & Related Disorders","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":24,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Alberta; Université Laval; McGill University; University of Ottawa; Hospital for Sick Children; SickKids Foundation; Montreal Neurological Institute and Hospital; Université de Sherbrooke; University of Toronto; McMaster University; Alberta Children's Hospital; Children's Hospital of Eastern Ontario","funders":"Canadian Institutes of Health Research","keywords":"Hereditary spastic paraplegia; Genetics; Multiplex ligation-dependent probe amplification; Mutation; Genetic heterogeneity; Genotype; Copy-number variation; Biology; Exome sequencing; Gene; Medicine; Phenotype; Exon; Genome","score_opus":0.019730895033111047,"score_gpt":0.281625994044325,"score_spread":0.26189509901121394,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4225252429","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":[0.9923815,0.0002691374,0.0006350701,0.00022127706,0.000015096397,0.000031197313,0.000640692,0.000028464592,0.0057775206],"genre_scores_gemma":[0.9977253,0.00013186887,0.0004456916,0.00007032242,0.000021029373,0.0000074417826,0.00030535395,0.000013366701,0.0012795128],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9996947,0.00005218258,0.00003938917,0.0000798154,0.000068568435,0.000065396394],"domain_scores_gemma":[0.9995691,0.00015757658,0.00009460308,0.000018632236,0.00008888358,0.00007111514],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00026871383,0.0009206969,0.0003476816,0.0023549586,0.00090213754,0.0004401661,0.00048539962,0.0008053873,0.0070535187],"category_scores_gemma":[0.0012594004,0.00027174546,0.00042317598,0.0009990571,0.0007154922,0.00030215993,0.0005384904,0.0003136945,0.000536686],"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":[0.002768067,0.00060307083,0.49600706,0.00023882491,0.0003328533,0.29189953,0.0014811119,0.0015182974,0.17084521,0.0033835352,0.0022812025,0.028641224],"study_design_scores_gemma":[0.00008214027,0.0006731029,0.8022091,0.00006506896,0.00034520464,0.1707684,0.000631453,0.0019167147,0.018966066,0.0014631348,0.0028332868,0.000046317637],"about_ca_topic_score_codex":0.0064412206,"about_ca_topic_score_gemma":0.0051875915,"teacher_disagreement_score":0.0070535187,"about_ca_system_score_codex":0.00043406076,"about_ca_system_score_gemma":0.00063622184,"threshold_uncertainty_score":0.023596406},"labels":[],"label_agreement":null},{"id":"W4226289364","doi":"10.1016/j.cont.2022.100022","title":"Lower urinary tract dysfunction in uncommon neurological diseases: A report of the neurourology promotion committee of the International Continence Society","year":2022,"lang":"en","type":"article","venue":"Continence","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":11,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Western University","funders":"","keywords":"Medicine; Neuromyelitis optica; Transverse myelitis; Pathology; Acute disseminated encephalomyelitis; Multiple sclerosis; Disease; Immunology","score_opus":0.025241215314651178,"score_gpt":0.24748335694609483,"score_spread":0.22224214163144365,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4226289364","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":[0.36067998,0.38593528,0.005543889,0.15482491,0.028697072,0.0006001177,0.00072675286,0.00031540866,0.06267663],"genre_scores_gemma":[0.65767473,0.2587494,0.004844362,0.031353682,0.025453065,0.00039443997,0.0016480839,0.00010661337,0.019775521],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.99859625,0.00034058522,0.00031638704,0.000101771686,0.00037107794,0.00027394053],"domain_scores_gemma":[0.9970393,0.00044002317,0.00066621683,0.00011534573,0.0008881734,0.0008509512],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.002956712,0.00043026393,0.0002987256,0.0020657924,0.0011892731,0.0009870093,0.0005093473,0.0017366137,0.0007803611],"category_scores_gemma":[0.003634562,0.00018681765,0.00035358235,0.0015750328,0.0008086952,0.00094565324,0.0011345089,0.0012671099,0.00027202335],"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":[0.000121074416,0.00038726415,0.27397624,0.0017989293,0.000088022214,0.06188142,0.005583522,0.00069371314,0.004999724,0.0033889192,0.28887686,0.3582044],"study_design_scores_gemma":[0.000027628506,0.00033688694,0.18370116,0.0036186737,0.00008805083,0.09412972,0.0035480491,0.0006724569,0.001917291,0.0006589635,0.7112136,0.00008758685],"about_ca_topic_score_codex":0.0029887669,"about_ca_topic_score_gemma":0.0062722913,"teacher_disagreement_score":0.0029887669,"about_ca_system_score_codex":0.0008639634,"about_ca_system_score_gemma":0.0039010304,"threshold_uncertainty_score":0.015636802},"labels":[],"label_agreement":null},{"id":"W4233669901","doi":"10.1111/j.1399-0004.2011.01665.x","title":"Addendum to ‘Recent advances in the genetics of distal hereditary motor neuropathy give insight to a disease mechanism involving copper homeostasis that may extend to other motor neuron disorders’","year":2011,"lang":"en","type":"letter","venue":"Clinical Genetics","topic":"Hereditary Neurological Disorders","field":"Neuroscience","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":"Centre Hospitalier Universitaire Sainte-Justine; Université de Montréal; Centre Hospitalier de l’Université de Montréal","funders":"","keywords":"Excellence; Center of excellence; Motor neuron; Medicine; Library science; Neuroscience; Psychology; Disease; Political science; Law; Internal medicine; Computer science","score_opus":0.09950021878439085,"score_gpt":0.323427463180901,"score_spread":0.22392724439651013,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4233669901","genre_codex":"commentary","genre_gemma":"other","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"other","genre_consensus":null,"domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.0011884823,0.002011766,0.00042198045,0.8973571,0.09229557,0.000040842413,0.00012827704,0.000105224375,0.0064507313],"genre_scores_gemma":[0.011225163,0.0024163504,0.0010262734,0.7481085,0.20909323,0.00007829603,0.000144905,0.000050715073,0.027856514],"study_design_codex":"not_applicable","study_design_gemma":"not_applicable","domain_scores_codex":[0.9980545,0.00039642784,0.00025380286,0.00033730367,0.00058932643,0.0003686682],"domain_scores_gemma":[0.9950428,0.0026767177,0.00047305017,0.00020702346,0.00096788775,0.0006324348],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0013214591,0.0015381038,0.0017829355,0.0007008567,0.0021648235,0.002453958,0.0027316916,0.037936248,0.009074496],"category_scores_gemma":[0.015539811,0.00071036257,0.0018283215,0.0005446941,0.0026146316,0.0021250218,0.0010996667,0.028801776,0.007214404],"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":[0.00012324525,0.00009645193,0.0008812626,0.00014366349,0.00004035974,0.0155387875,0.0001024603,0.00016437599,0.00043463992,0.001922277,0.97071517,0.009837247],"study_design_scores_gemma":[0.0003258831,0.00036270285,0.0077406643,0.0003243783,0.00013656674,0.027746009,0.00041361531,0.0024467248,0.0009163391,0.0114509575,0.94794095,0.0001952862],"about_ca_topic_score_codex":0.0032933143,"about_ca_topic_score_gemma":0.008428182,"teacher_disagreement_score":0.037936248,"about_ca_system_score_codex":0.003013439,"about_ca_system_score_gemma":0.0018036512,"threshold_uncertainty_score":0.030357242},"labels":[],"label_agreement":null},{"id":"W4236830967","doi":"10.3410/f.4517973.4376079","title":"Faculty Opinions recommendation of Reversal of neuropathy phenotypes in conditional mouse model of Charcot-Marie-Tooth disease type 2E.","year":2010,"lang":"en","type":"dataset","venue":"Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature","topic":"Hereditary Neurological Disorders","field":"Neuroscience","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":"Phenotype; Doxycycline; Transgene; Genetically modified mouse; Spinal muscular atrophy; Disease; Neurofilament; Mutant; Muscle atrophy; Medicine; Neuroscience; Biology; Gene; Pathology; Endocrinology; Atrophy; Internal medicine; Genetics; Immunohistochemistry","score_opus":0.05068552332750072,"score_gpt":0.3383308866961783,"score_spread":0.2876453633686776,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4236830967","genre_codex":"dataset","genre_gemma":"dataset","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"dataset","genre_consensus":"dataset","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.0036151323,0.0002758859,0.00046978713,0.0004947449,0.00010460059,0.00006064595,0.985045,0.0018962201,0.008037985],"genre_scores_gemma":[0.0080088265,0.0003474176,0.002760626,0.00014152417,0.000031971635,0.00013647861,0.98169035,0.00036983626,0.0065129185],"study_design_codex":"not_applicable","study_design_gemma":"not_applicable","domain_scores_codex":[0.9990067,0.00012370011,0.00009903382,0.00024276564,0.00043156854,0.00009616765],"domain_scores_gemma":[0.9954253,0.0010421764,0.0006731219,0.00060332735,0.0015940857,0.00066195463],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0012736996,0.0008536169,0.0005175045,0.004732336,0.00044144373,0.0010555821,0.0008987889,0.00058857823,0.057134196],"category_scores_gemma":[0.0073085357,0.00023875809,0.0005834086,0.0058187153,0.00018539926,0.00069517083,0.0007454892,0.00069914025,0.022955596],"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":[0.00019632772,0.00004899891,0.009022586,0.00096880604,0.00011798128,0.00008482902,0.00004315858,0.0003450433,0.0018038789,0.0007356345,0.96147543,0.025157103],"study_design_scores_gemma":[0.00022608267,0.000046856698,0.033012643,0.00021987123,0.00014421322,0.00014216844,0.00009940018,0.0021342114,0.0040029916,0.00059031683,0.9593435,0.000037748785],"about_ca_topic_score_codex":0.032705747,"about_ca_topic_score_gemma":0.09795895,"teacher_disagreement_score":0.057134196,"about_ca_system_score_codex":0.0012582252,"about_ca_system_score_gemma":0.003512236,"threshold_uncertainty_score":0.1911329},"labels":[],"label_agreement":null},{"id":"W4242308290","doi":"10.1007/s12098-015-1916-y","title":"Imaging in Pediatric Demyelinating and Inflammatory Diseases of the Brain- Part 1","year":2015,"lang":"en","type":"review","venue":"The Indian Journal of Pediatrics","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":6,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Hospital for Sick Children","funders":"","keywords":"Medicine; Neuroimaging; Demyelinating Disorder; Modality (human–computer interaction); Susceptibility weighted imaging; Multiple sclerosis; Magnetic resonance imaging; Medical imaging; Radiology; Immunology; Artificial intelligence","score_opus":0.04443427248525553,"score_gpt":0.3013065225971762,"score_spread":0.2568722501119207,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4242308290","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":[0.0002233412,0.99849904,0.0001467785,0.00020716741,0.0001128584,0.0000035791834,0.000016456992,0.0000060842517,0.0007846109],"genre_scores_gemma":[0.0024450347,0.9960014,0.00043186863,0.00022759136,0.0005297505,0.0000052096625,0.000038439935,0.000002938422,0.00031765227],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.9997397,0.000048952563,0.000062777435,0.000049047987,0.000066697816,0.000032789434],"domain_scores_gemma":[0.9992379,0.0004102964,0.00013555355,0.000018014267,0.00014237805,0.000055891913],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0005126963,0.001110515,0.001528545,0.004812075,0.00027322109,0.0011877946,0.0011116794,0.0014050779,0.0019859408],"category_scores_gemma":[0.0012561975,0.00041179627,0.00064669095,0.0032210387,0.00091677526,0.0015995305,0.000711995,0.0018359562,0.0010602291],"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":[0.00008669713,0.00009146377,0.0023176156,0.018397667,0.00015507377,0.006159491,0.00014063453,0.0007101721,0.0029069218,0.0027469452,0.032484844,0.9338025],"study_design_scores_gemma":[0.000047043988,0.00016121597,0.012767246,0.017270656,0.0006929962,0.13040923,0.00038615544,0.0005307835,0.0023251094,0.0049111554,0.8303787,0.00011959595],"about_ca_topic_score_codex":0.0027200072,"about_ca_topic_score_gemma":0.0033481186,"teacher_disagreement_score":0.004812075,"about_ca_system_score_codex":0.0007899431,"about_ca_system_score_gemma":0.0012837425,"threshold_uncertainty_score":0.0066435933},"labels":[],"label_agreement":null},{"id":"W4244821111","doi":"10.1093/jcag/gwy009.025","title":"A25 COLONIC PROTEASES EVOKE SUSTAINED PAIN SIGNALING VIA A NOVEL ENDOSOMAL PATHWAY IN NEURONS","year":2018,"lang":"en","type":"article","venue":"Journal of the Canadian Association of Gastroenterology","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":false,"ca_institutions":"Queen's University","funders":"","keywords":"Proteases; Endosome; Cell biology; Cathepsin G; Cathepsin; Elastase; Antagonist; Chemistry; Signal transduction; Cathepsin B; Trypsin; Receptor; Biology; Biochemistry; Enzyme","score_opus":0.015233201988055015,"score_gpt":0.22268516346733083,"score_spread":0.2074519614792758,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4244821111","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":[0.99416804,0.002074588,0.0013333298,0.0001626918,0.00004225209,0.00003271699,0.00034006327,0.000037236947,0.0018089453],"genre_scores_gemma":[0.99489516,0.001310404,0.0015389489,0.00013033784,0.000022087648,0.000067506066,0.00021915835,0.000007999578,0.0018083687],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9998944,0.000012660181,0.000008522507,0.00001671053,0.000023029148,0.00004471701],"domain_scores_gemma":[0.99996316,0.0000059060894,0.0000075936427,0.000004421356,0.000005300191,0.000013685279],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00010637459,0.00026584422,0.0003428083,0.00013074225,0.00015354335,0.00029956063,0.0001648366,0.00038272495,0.0010724519],"category_scores_gemma":[0.0001026212,0.00012787021,0.00045364015,0.00011509262,0.00016650776,0.00027866813,0.00019125688,0.0005837929,0.0003347145],"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":[0.00028690483,0.000017834154,0.00009636943,0.00004670947,0.000006931145,0.00012260316,0.0000102261565,0.00002292811,0.99861693,0.000047814094,0.000034416615,0.00069035875],"study_design_scores_gemma":[0.00019286052,0.0025469598,0.06772718,0.00004388844,0.000091494054,0.0010745068,0.00023284592,0.0018768503,0.92357415,0.0002867596,0.0023317717,0.000020734598],"about_ca_topic_score_codex":0.0007727286,"about_ca_topic_score_gemma":0.0014016757,"teacher_disagreement_score":0.0010724519,"about_ca_system_score_codex":0.00033946097,"about_ca_system_score_gemma":0.00017823988,"threshold_uncertainty_score":0.0035877824},"labels":[],"label_agreement":null},{"id":"W4248129186","doi":"10.1017/9781139939508.097","title":"DOG1","year":2016,"lang":"en","type":"book-chapter","venue":"Cambridge University Press eBooks","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":false,"ca_institutions":"University of Toronto","funders":"","keywords":"Computer science","score_opus":0.04284265721507148,"score_gpt":0.2065195742171871,"score_spread":0.16367691700211562,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4248129186","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":[0.0068537816,0.06549844,0.017778715,0.0055328268,0.0071423124,0.00022292357,0.068534434,0.008565397,0.81987125],"genre_scores_gemma":[0.02130028,0.0397217,0.011236266,0.0028157425,0.000708485,0.00023099591,0.11597094,0.0029333448,0.8050822],"study_design_codex":"not_applicable","study_design_gemma":"not_applicable","domain_scores_codex":[0.99981016,0.000014020382,0.0000128229285,0.000045642468,0.000090398724,0.00002693052],"domain_scores_gemma":[0.9998273,0.00003291657,0.000013818848,0.000020713886,0.000055363176,0.000049833772],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.000343437,0.0006852049,0.0007093922,0.0014884114,0.0004471707,0.0015786573,0.0011702167,0.000794135,0.29049757],"category_scores_gemma":[0.00049896137,0.0003008555,0.0004800055,0.0016353623,0.00025530055,0.0016682191,0.0006933239,0.0011776086,0.23621891],"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":[0.00016050045,0.0000471129,0.00030671555,0.0014288017,0.000016774895,0.00039659455,0.000069267124,0.00024320648,0.020464832,0.010283972,0.6985756,0.26800653],"study_design_scores_gemma":[0.0000032378437,0.000011443639,0.0002230979,0.00005439747,0.00000490788,0.0003827545,0.000011702332,0.000037642352,0.0015477205,0.0005578036,0.9971603,0.0000050203494],"about_ca_topic_score_codex":0.001097389,"about_ca_topic_score_gemma":0.0014726061,"teacher_disagreement_score":0.29049757,"about_ca_system_score_codex":0.0007352199,"about_ca_system_score_gemma":0.00060368946,"threshold_uncertainty_score":0},"labels":[],"label_agreement":null},{"id":"W4251531443","doi":"10.1017/cjn.2017.156","title":"P.072 Effects of self-directed exercise on strength in Charcot-Marie-Tooth disease subtypes","year":2017,"lang":"en","type":"article","venue":"Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":0,"is_retracted":false,"has_abstract":true,"route_ca_aff":false,"route_ca_fund":false,"route_ca_venue":true,"route_about_ca":false,"ca_institutions":"","funders":"","keywords":"Medicine; Grip strength; Physical therapy; Tooth disease; Population; Disease; Physical medicine and rehabilitation; Pes cavus; Elbow; Internal medicine; Surgery","score_opus":0.025732283266106572,"score_gpt":0.26210025296007494,"score_spread":0.23636796969396837,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4251531443","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":[0.997357,0.0009424005,0.000031146898,0.0001107355,0.000014875992,0.000018946144,0.0004123414,0.000002971121,0.001109656],"genre_scores_gemma":[0.99886274,0.00020259178,0.000098023236,0.000040587965,0.000014530099,0.000019745035,0.00038379483,0.0000022038596,0.0003758477],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9995597,0.00013798723,0.000048995636,0.00007638649,0.000119135206,0.000057806166],"domain_scores_gemma":[0.9973992,0.00073506887,0.0010359966,0.00009432762,0.00022366676,0.0005117767],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0010909348,0.00021269845,0.00038694532,0.00060781173,0.00042312816,0.0004900955,0.0005539834,0.00042188182,0.0054677967],"category_scores_gemma":[0.003779738,0.00011838304,0.00084290694,0.0007144232,0.00025434306,0.00028734296,0.0003251096,0.00042537335,0.0004399807],"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":[0.00091852533,0.00010837968,0.99196965,0.00003951713,0.00016782347,0.00008605765,0.000044207056,0.000032315904,0.00012682655,0.0000114488075,0.00021400952,0.006281254],"study_design_scores_gemma":[0.00002895499,0.00037401228,0.999006,0.000024639936,0.000051510448,0.00019978144,0.00007177454,0.00006785394,0.000026070666,0.000017814034,0.00012959585,0.0000020269251],"about_ca_topic_score_codex":0.009432195,"about_ca_topic_score_gemma":0.0147557845,"teacher_disagreement_score":0.009432195,"about_ca_system_score_codex":0.00037529835,"about_ca_system_score_gemma":0.0003744517,"threshold_uncertainty_score":0.018754601},"labels":[],"label_agreement":null},{"id":"W4280491100","doi":"10.1017/cjn.2022.59","title":"Childhood-Onset Writer’s Cramp in Hereditary Spastic Paraplegia Type 15","year":2022,"lang":"en","type":"article","venue":"Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":0,"is_retracted":false,"has_abstract":true,"route_ca_aff":false,"route_ca_fund":false,"route_ca_venue":true,"route_about_ca":false,"ca_institutions":"","funders":"","keywords":"Paraplegia; Hereditary spastic paraplegia; Spastic; Medicine; Spastic quadriplegia; Pediatrics; Physical medicine and rehabilitation; Cerebral palsy; Spinal cord; Genetics; Psychiatry","score_opus":0.04316926395045465,"score_gpt":0.26706122087952017,"score_spread":0.22389195692906552,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4280491100","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":[0.9872333,0.00094722776,0.00041566085,0.00070223154,0.00012851483,0.000069727066,0.0007454322,0.000091715694,0.009666234],"genre_scores_gemma":[0.9974898,0.00040703648,0.00020520104,0.00015581524,0.000099370875,0.000008324896,0.00023602755,0.000017368056,0.0013810036],"study_design_codex":"case_report","study_design_gemma":"case_report","domain_scores_codex":[0.99950314,0.000042701453,0.00005762808,0.000110753754,0.000104379644,0.00018138022],"domain_scores_gemma":[0.99885666,0.00035952782,0.0002903778,0.000042115495,0.000097917255,0.00035343185],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00021667748,0.0009354781,0.00074676017,0.0020354155,0.0011411433,0.00074560253,0.0004918798,0.001452266,0.0069090645],"category_scores_gemma":[0.0018012278,0.00043913806,0.0004905877,0.0016906866,0.0009868921,0.00060283975,0.0005744902,0.0009890274,0.00090148504],"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":[0.0003372515,0.00009693308,0.112909175,0.00010185098,0.00004696716,0.8761503,0.00042168843,0.00022795521,0.0023932008,0.0003177256,0.0016033414,0.0053936956],"study_design_scores_gemma":[0.00006343229,0.0002580181,0.2482922,0.00009894807,0.00007987964,0.7477646,0.00065980514,0.0003163042,0.0010425854,0.00035202157,0.0010301209,0.000042030195],"about_ca_topic_score_codex":0.023140766,"about_ca_topic_score_gemma":0.021131445,"teacher_disagreement_score":0.023140766,"about_ca_system_score_codex":0.0011391183,"about_ca_system_score_gemma":0.0011019323,"threshold_uncertainty_score":0.046012104},"labels":[],"label_agreement":null},{"id":"W4280506782","doi":"10.1186/s12883-022-02708-z","title":"Genetic origin of patients having spastic paraplegia with or without other neurologic manifestations","year":2022,"lang":"en","type":"article","venue":"BMC Neurology","topic":"Hereditary Neurological Disorders","field":"Neuroscience","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":"","keywords":"Medicine; Hereditary spastic paraplegia; Ataxia; Paraplegia; Pathology; Neurology; Corpus callosum; Acute disseminated encephalomyelitis; Pseudobulbar palsy; Disease; Spinal cord; Genetics; Biology","score_opus":0.05536126730778658,"score_gpt":0.2728350880262508,"score_spread":0.21747382071846422,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4280506782","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":[0.99853563,0.00020622408,0.000103635284,0.00006167917,0.000008438495,0.00001602422,0.00013153319,0.0000069093376,0.0009299331],"genre_scores_gemma":[0.9994796,0.0000711051,0.000092123,0.000039392944,0.000016369573,0.000008074067,0.00016509018,0.0000043221607,0.00012404085],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9997452,0.0000375363,0.000029153174,0.00008022657,0.000048071877,0.000059857688],"domain_scores_gemma":[0.9991105,0.00018346403,0.00031444474,0.00005216044,0.00010945133,0.00022995178],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00020364102,0.0006604663,0.0003677592,0.0008819506,0.0007722567,0.00031301097,0.00036232054,0.00078716327,0.006755946],"category_scores_gemma":[0.0013696437,0.00017893838,0.00033831468,0.00059510383,0.0004336098,0.00019055953,0.00043056757,0.00042739182,0.0007908571],"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":[0.00037237233,0.000113358954,0.96831423,0.000036562597,0.000065908775,0.022625128,0.00030830412,0.00012339534,0.0047670314,0.00017172398,0.0003402499,0.0027616536],"study_design_scores_gemma":[0.00006621765,0.000386881,0.875985,0.000046165118,0.00013196107,0.11981424,0.00046588358,0.00041457632,0.001337521,0.00028727614,0.0010387644,0.000025543035],"about_ca_topic_score_codex":0.0013436,"about_ca_topic_score_gemma":0.0009743775,"teacher_disagreement_score":0.006755946,"about_ca_system_score_codex":0.0002189695,"about_ca_system_score_gemma":0.00042798705,"threshold_uncertainty_score":0.02260089},"labels":[],"label_agreement":null},{"id":"W4280572211","doi":"10.3390/muscles1010007","title":"Distinct Phenotypic and microRNA Expression in X-Linked Charcot–Marie–Tooth Correlated with a Novel Mutation in the GJB1 Gene","year":2022,"lang":"en","type":"article","venue":"Muscles","topic":"Hereditary Neurological Disorders","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":"Advanced Foods and Materials Canada","keywords":"Frameshift mutation; Connexin 32; Genetics; Connexin; Biology; Mutation; Phenotype; Gene; Gap junction","score_opus":0.03066600000118135,"score_gpt":0.23172499096404087,"score_spread":0.2010589909628595,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4280572211","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":[0.99942243,0.000117194046,0.00017022679,0.00002712177,0.00000629789,0.0000069073208,0.000047507812,0.000012339375,0.00018985498],"genre_scores_gemma":[0.9992656,0.0000682873,0.00023932345,0.000029142857,0.000012390204,0.000008198372,0.000060784016,0.000007682951,0.0003086758],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9996723,0.0000457709,0.000040550032,0.00012404867,0.000075042255,0.000042270527],"domain_scores_gemma":[0.99952745,0.00013483244,0.00016670079,0.000026950494,0.000029457682,0.000114658236],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00027318383,0.001044754,0.00045985548,0.00085606874,0.0004972419,0.0002926482,0.00025934115,0.0008207901,0.0015595134],"category_scores_gemma":[0.00090617023,0.00039202085,0.00032475273,0.0003039849,0.0005472523,0.00016792586,0.00039835225,0.00039865653,0.00024226242],"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":[0.0012372587,0.00036454486,0.13317749,0.00015314823,0.00014836212,0.4258395,0.0012117779,0.00024743474,0.43321443,0.00024179296,0.00032292985,0.003841265],"study_design_scores_gemma":[0.000085790845,0.0008015437,0.56622374,0.000026468479,0.00013787956,0.41071206,0.0003574886,0.0013595939,0.019208709,0.0001629374,0.00088862306,0.000035222965],"about_ca_topic_score_codex":0.0006664412,"about_ca_topic_score_gemma":0.0006883692,"teacher_disagreement_score":0.0015595134,"about_ca_system_score_codex":0.00020054626,"about_ca_system_score_gemma":0.00016526262,"threshold_uncertainty_score":0.005217135},"labels":[],"label_agreement":null},{"id":"W4283643925","doi":"10.1177/2329048x221108826","title":"<i>NTRK1</i> -related Hereditary Sensory and Autonomic Neuropathy Type 4: The Role of the Histamine Challenge Test","year":2022,"lang":"en","type":"article","venue":"Child Neurology Open","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":4,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Children's Hospital of Eastern Ontario; McGill University","funders":"","keywords":"Medicine; Hypotonia; Histamine; Diabetic neuropathy; Internal medicine; Endocrinology; Diabetes mellitus","score_opus":0.01721389677677416,"score_gpt":0.21785147640887534,"score_spread":0.2006375796321012,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4283643925","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":[0.98299307,0.0025420454,0.0025031117,0.0011884548,0.00008654883,0.000029469657,0.00010898643,0.00015650582,0.010391835],"genre_scores_gemma":[0.997044,0.00048772313,0.0014214332,0.00025523518,0.000047306603,0.0000039992433,0.000038913204,0.000018057082,0.0006833226],"study_design_codex":"case_report","study_design_gemma":"case_report","domain_scores_codex":[0.999845,0.000033583292,0.00002167761,0.00003561509,0.000035647434,0.000028435228],"domain_scores_gemma":[0.9996612,0.00017145059,0.000087142434,0.000012773347,0.00002038998,0.000047127516],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00018772975,0.0006021627,0.00036219088,0.00031192455,0.00033554743,0.00036866235,0.00033468165,0.00076349196,0.0013956771],"category_scores_gemma":[0.0008067252,0.00010334702,0.00015626462,0.00014104009,0.0005761879,0.0004013037,0.0002608439,0.0004609957,0.00027488233],"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":[0.00043032892,0.00010219103,0.15430254,0.00016419357,0.00006140921,0.7213534,0.0004655655,0.0005229933,0.08753893,0.0007979336,0.0015178683,0.03274264],"study_design_scores_gemma":[0.000021820242,0.00027193167,0.091047466,0.00006974338,0.00005796902,0.87766105,0.00029515492,0.0015193797,0.024333589,0.00074145815,0.003956078,0.000024346951],"about_ca_topic_score_codex":0.0014392382,"about_ca_topic_score_gemma":0.0015538994,"teacher_disagreement_score":0.0014392382,"about_ca_system_score_codex":0.0002749712,"about_ca_system_score_gemma":0.0002000684,"threshold_uncertainty_score":0.0046690106},"labels":[],"label_agreement":null},{"id":"W4283768532","doi":"10.3899/jrheum.220017","title":"Getting the Diagnosis Right: What’s in a Name?","year":2022,"lang":"en","type":"article","venue":"The Journal of Rheumatology","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":1,"is_retracted":false,"has_abstract":false,"route_ca_aff":false,"route_ca_fund":false,"route_ca_venue":true,"route_about_ca":false,"ca_institutions":"","funders":"","keywords":"Medicine","score_opus":0.02859505068382786,"score_gpt":0.26109757252980287,"score_spread":0.232502521845975,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4283768532","genre_codex":"commentary","genre_gemma":"commentary","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"commentary","genre_consensus":"commentary","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.0015830209,0.07976354,0.0018260521,0.8690449,0.040175095,0.000016182275,0.000085287335,0.000119656834,0.007386225],"genre_scores_gemma":[0.056180514,0.13466148,0.008065938,0.6831596,0.10562127,0.00008936196,0.00024022389,0.00037650496,0.011605115],"study_design_codex":"not_applicable","study_design_gemma":"not_applicable","domain_scores_codex":[0.9888969,0.0041058287,0.0018309157,0.0010638011,0.0026819133,0.0014206439],"domain_scores_gemma":[0.965326,0.016292717,0.0024573929,0.0012229792,0.01011157,0.0045892284],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.009320794,0.0010478937,0.0029747302,0.0018438841,0.00562323,0.009157682,0.0020566639,0.015285813,0.012481674],"category_scores_gemma":[0.051785424,0.00045774857,0.0015391103,0.0013205518,0.010454263,0.020746278,0.0029816267,0.02177276,0.006340775],"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":[0.00043112345,0.00029964006,0.010444316,0.0029139533,0.00027274576,0.007373701,0.0033490362,0.00022958934,0.0013222756,0.02760615,0.65756696,0.2881904],"study_design_scores_gemma":[0.00019475208,0.00027120023,0.005004071,0.013658213,0.00037487247,0.03471378,0.014410735,0.00034743155,0.00088851934,0.084886625,0.84485966,0.00039025393],"about_ca_topic_score_codex":0.007903596,"about_ca_topic_score_gemma":0.0109595405,"teacher_disagreement_score":0.015285813,"about_ca_system_score_codex":0.0037454686,"about_ca_system_score_gemma":0.007817013,"threshold_uncertainty_score":0.049293697},"labels":[],"label_agreement":null},{"id":"W4287832190","doi":"10.1002/mds.29147","title":"<i>MED27</i>, <i>SLC6A7,</i> and <i>MPPE1</i> Variants in a Complex Neurodevelopmental Disorder with Severe Dystonia","year":2022,"lang":"en","type":"article","venue":"Movement Disorders","topic":"Hereditary Neurological Disorders","field":"Neuroscience","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":"Université de Montréal; Centre Hospitalier Universitaire Sainte-Justine","funders":"National Cancer Institute; National Medical Research Council; Medical Research Council; Canadian Institutes of Health Research; Medical Research Council Canada; NIHR Cambridge Biomedical Research Centre; Rosetrees Trust; National Institutes of Health; National Health and Medical Research Council; University of Cambridge; NBIA Disorders Association; National Institute for Health and Care Research; Sir Jules Thorn Charitable Trust; T.L.L Temple Foundation; Deutsche Forschungsgemeinschaft; UK Research and Innovation; Wellcome Trust","keywords":"Zebrafish; Exome sequencing; Dystonia; Phenotype; Neurodevelopmental disorder; Biology; Candidate gene; Intellectual disability; Genetics; Movement disorders; Epilepsy; Gene knockdown; Gene; Disease; Neuroscience; Medicine; Internal medicine","score_opus":0.015774071347260686,"score_gpt":0.21471063153019967,"score_spread":0.19893656018293898,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4287832190","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":[0.99793553,0.0002768069,0.0007997592,0.00013186874,0.000010597563,0.00001360353,0.00019430164,0.000038599745,0.0005990245],"genre_scores_gemma":[0.9980533,0.0001600235,0.0012332383,0.00007455473,0.00002126689,0.0000062786253,0.00014295932,0.000017061295,0.0002912579],"study_design_codex":"case_report","study_design_gemma":"observational","domain_scores_codex":[0.9998159,0.000016626973,0.000023559887,0.00007544176,0.000037700942,0.000030804316],"domain_scores_gemma":[0.99974364,0.00008998142,0.00007789174,0.000013551454,0.000017262186,0.000057563997],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00015112852,0.0011685754,0.00031340544,0.00089250033,0.0005976389,0.00034863417,0.00036680035,0.0009951517,0.001688387],"category_scores_gemma":[0.0005323825,0.00025025214,0.0005199802,0.0004977085,0.00075389823,0.00024106818,0.00048124054,0.0004813656,0.00027821792],"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":[0.000601881,0.00010063172,0.18556473,0.00015040385,0.00016988254,0.53595686,0.0011595156,0.00112345,0.2635434,0.00088108133,0.00089464575,0.009853613],"study_design_scores_gemma":[0.00006014179,0.0003002857,0.2287952,0.00006910998,0.00037044755,0.7049115,0.00054264115,0.0028613552,0.05780711,0.00061387755,0.0036214546,0.00004686863],"about_ca_topic_score_codex":0.0018614163,"about_ca_topic_score_gemma":0.002394805,"teacher_disagreement_score":0.0018614163,"about_ca_system_score_codex":0.00038424224,"about_ca_system_score_gemma":0.00031708408,"threshold_uncertainty_score":0.0056482553},"labels":[],"label_agreement":null},{"id":"W4289028824","doi":"10.1093/hmg/ddac170","title":"A novel mouse model of CMT1B identifies hyperglycosylation as a new pathogenetic mechanism","year":2022,"lang":"en","type":"article","venue":"Human Molecular Genetics","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":12,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Centre for Movement Disorders","funders":"Fondazione Centro San Raffaele; Eunice Kennedy Shriver National Institute of Child Health and Human Development","keywords":"Myelin; Biology; Endoplasmic reticulum; Phenotype; Unfolded protein response; Mutant; Mutation; Cell biology; Glycosylation; Loss function; Gene; Neuroscience; Genetics; Central nervous system","score_opus":0.05704764243102658,"score_gpt":0.2648321849678463,"score_spread":0.2077845425368197,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4289028824","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":[0.9496901,0.0027933083,0.030437248,0.0015469826,0.00053727196,0.00032275723,0.006545057,0.0014061586,0.006721013],"genre_scores_gemma":[0.9381526,0.0042104963,0.028168777,0.00055317406,0.00010317453,0.0008554762,0.0050584967,0.00055082364,0.02234684],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.999506,0.000049171154,0.000049633618,0.00018537403,0.00014814173,0.00006171945],"domain_scores_gemma":[0.99963,0.000035970646,0.0001428807,0.000033857294,0.00002744966,0.00012993466],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0002920595,0.0015725213,0.0004888144,0.00174077,0.00051193114,0.0006447567,0.0006922236,0.0018048794,0.00487894],"category_scores_gemma":[0.00026404342,0.00055509334,0.00065588666,0.00070158247,0.0009383985,0.0006237291,0.00067061087,0.0022787906,0.0014448803],"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":[0.00032548237,0.00011442178,0.00019116848,0.00008978722,0.000015174774,0.000533464,0.000046628727,0.00012027066,0.9953243,0.0008589146,0.0003036654,0.0020768507],"study_design_scores_gemma":[0.000565239,0.0017056551,0.00938352,0.00020269833,0.00014150704,0.011636756,0.00014099489,0.005220853,0.93865377,0.001274183,0.030998753,0.000076076634],"about_ca_topic_score_codex":0.00085202255,"about_ca_topic_score_gemma":0.0011238711,"teacher_disagreement_score":0.00487894,"about_ca_system_score_codex":0.0006225562,"about_ca_system_score_gemma":0.000408326,"threshold_uncertainty_score":0.01632166},"labels":[],"label_agreement":null},{"id":"W4298147486","doi":"10.3389/fneur.2022.1005670","title":"Clinical and genetic characterization of a Taiwanese cohort with spastic paraparesis combined with cerebellar involvement","year":2022,"lang":"en","type":"article","venue":"Frontiers in Neurology","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":4,"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":"Cerebellar ataxia; Ataxia; Population; Hereditary spastic paraplegia; Medicine; Pathology; Genetic testing; Spinocerebellar ataxia; Neuroscience; Biology; Genetics; Phenotype; Internal medicine; Gene","score_opus":0.014833565994701257,"score_gpt":0.22576806352444165,"score_spread":0.2109344975297404,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4298147486","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":[0.9997682,0.000027268217,0.000030359672,0.000009728153,7.9218825e-7,0.000004093376,0.000047540427,0.0000015314761,0.00011041102],"genre_scores_gemma":[0.99963737,0.000043842294,0.00004165343,0.000013001439,0.0000037106151,0.0000061164515,0.00015991517,0.0000017034102,0.000092714],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9997422,0.000042718755,0.000029637526,0.00010011884,0.000031481988,0.000053815565],"domain_scores_gemma":[0.9995371,0.00007766878,0.00011483049,0.000054638742,0.00007070637,0.00014503424],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0002572089,0.00044188934,0.00038314785,0.0011440973,0.00068477995,0.00050102646,0.00026182935,0.0003839969,0.0015830533],"category_scores_gemma":[0.0011537195,0.00027257996,0.00029703352,0.00091875286,0.00034205252,0.0002538428,0.00059468707,0.00027440523,0.00030463564],"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":[0.000079328835,0.000030776573,0.9913639,0.000005583538,0.000032942513,0.0040713027,0.00045678986,0.000047984035,0.002375771,0.000025076813,0.00008093729,0.0014296114],"study_design_scores_gemma":[0.000008548339,0.00013178572,0.9888509,0.000007008468,0.00003093945,0.009559487,0.0006794722,0.00024343444,0.0002065491,0.000033572123,0.00024074568,0.0000075961366],"about_ca_topic_score_codex":0.0067684273,"about_ca_topic_score_gemma":0.0047200737,"teacher_disagreement_score":0.0067684273,"about_ca_system_score_codex":0.00024629742,"about_ca_system_score_gemma":0.0003401471,"threshold_uncertainty_score":0.013458073},"labels":[],"label_agreement":null},{"id":"W4307229213","doi":"10.1080/00207454.2022.2140428","title":"<i>KIF1A</i> novel frameshift variant p.(Ser887Profs*64) exhibits clinical heterogeneity in a Pakistani family with hereditary sensory and autonomic neuropathy type IIC","year":2022,"lang":"en","type":"article","venue":"International Journal of Neuroscience","topic":"Hereditary Neurological Disorders","field":"Neuroscience","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","funders":"Higher Education Commision, Pakistan","keywords":"Penetrance; Frameshift mutation; Disease gene identification; Proband; Genetics; Exome sequencing; Genetic heterogeneity; Exome; Single-nucleotide polymorphism; Biology; Family history; Medicine; Mutation; Gene; Internal medicine; Genotype; Phenotype","score_opus":0.07598084139042191,"score_gpt":0.3300688681547659,"score_spread":0.25408802676434394,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4307229213","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":[0.9993917,0.00005665511,0.00014077948,0.000022470542,0.0000026859536,0.0000053984822,0.000085910564,0.0000047918384,0.00028946134],"genre_scores_gemma":[0.99954396,0.00004191244,0.00017158373,0.000019471754,0.0000053808913,0.0000041741814,0.00009733511,0.0000022742925,0.00011385336],"study_design_codex":"observational","study_design_gemma":"case_report","domain_scores_codex":[0.99990773,0.000008357755,0.0000097173815,0.00003899372,0.000017392715,0.00001772681],"domain_scores_gemma":[0.9997887,0.000058818325,0.000082089515,0.000011399615,0.000014675609,0.000044263583],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00010277085,0.00045149375,0.00021816071,0.0005048626,0.0005499649,0.00026217083,0.00019850362,0.0003788193,0.0015767914],"category_scores_gemma":[0.00036323187,0.00012232614,0.00016858667,0.0003578226,0.00040731483,0.00008874103,0.00025229255,0.0002893735,0.00021722895],"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":[0.0010966884,0.0002599881,0.457795,0.00015176597,0.00016044876,0.26510748,0.0015888936,0.00080420286,0.25288957,0.00044341266,0.0011722473,0.018530345],"study_design_scores_gemma":[0.00007127651,0.000510052,0.6874976,0.000039810668,0.00012152151,0.29347783,0.000673523,0.0009386725,0.01373294,0.00025403115,0.0026521015,0.000030615938],"about_ca_topic_score_codex":0.0017092616,"about_ca_topic_score_gemma":0.0018870843,"teacher_disagreement_score":0.0017092616,"about_ca_system_score_codex":0.00021678947,"about_ca_system_score_gemma":0.00015273382,"threshold_uncertainty_score":0.0052748322},"labels":[],"label_agreement":null},{"id":"W4307561089","doi":"10.1177/19418744221134175","title":"Subcortical Demyelinating Lesions Associated With Hereditary Neuropathy With Liability to Pressure Palsies","year":2022,"lang":"en","type":"article","venue":"The Neurohospitalist","topic":"Hereditary Neurological Disorders","field":"Neuroscience","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":"Western University","funders":"","keywords":"Medicine; Demyelinating disease; Neuroscience; Pathology; Psychology; Disease","score_opus":0.02238036349784745,"score_gpt":0.23189066621431853,"score_spread":0.2095103027164711,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4307561089","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":[0.98840827,0.00025364273,0.00053189864,0.00024311393,0.000025387373,0.000023459292,0.00008879632,0.000040681298,0.010384818],"genre_scores_gemma":[0.9986066,0.0001031088,0.00026564923,0.00007896042,0.00005131647,0.0000051704033,0.00005008209,0.000008977538,0.0008301931],"study_design_codex":"case_report","study_design_gemma":"case_report","domain_scores_codex":[0.99970883,0.000057735117,0.00003860831,0.000038476977,0.00005838839,0.000097902055],"domain_scores_gemma":[0.9985697,0.00051753334,0.00042468094,0.00006295304,0.00014020767,0.00028475942],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00025737964,0.0013141806,0.00042358483,0.0019108488,0.0010707557,0.000626943,0.0004819673,0.0011559685,0.007539241],"category_scores_gemma":[0.0023321074,0.00040305598,0.00020620276,0.0012531308,0.0009634955,0.00043007656,0.0008080582,0.00073286047,0.00053658424],"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":[0.0003967912,0.0001790048,0.10082827,0.00009178183,0.00008212172,0.8817,0.00061016215,0.00035182564,0.009497345,0.0011131639,0.0006683842,0.0044811675],"study_design_scores_gemma":[0.00007028512,0.0003362931,0.2149359,0.00004683664,0.00011196098,0.7764356,0.00063934055,0.0009834694,0.0038868769,0.0016965857,0.0008302844,0.000026608237],"about_ca_topic_score_codex":0.0033511736,"about_ca_topic_score_gemma":0.004894239,"teacher_disagreement_score":0.007539241,"about_ca_system_score_codex":0.00037548548,"about_ca_system_score_gemma":0.00056039955,"threshold_uncertainty_score":0.025221288},"labels":[],"label_agreement":null},{"id":"W4307842001","doi":"10.1093/brain/awac391","title":"The clinical and molecular spectrum of <i>ZFYVE26</i>-associated hereditary spastic paraplegia: SPG15","year":2022,"lang":"en","type":"article","venue":"Brain","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":23,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"SickKids Foundation; Hospital for Sick Children; University of Toronto","funders":"Manton Center for Orphan Disease Research, Boston Children's Hospital; Research Committee for Ataxic Disease; Intellectual and Developmental Disabilities Research Center; National Institutes of Health; Eunice Kennedy Shriver National Institute of Child Health and Human Development; University College London Hospitals NHS Foundation Trust; Brain Research UK; Deutsche Forschungsgemeinschaft; National Institute of Neurological Disorders and Stroke; National Institute for Health and Care Research; Ministero della Salute; Spastic Paraplegia Foundation; Wellcome Trust","keywords":"Hereditary spastic paraplegia; Parkinsonism; Spasticity; Medicine; Pediatrics; Movement disorders; Age of onset; Dystonia; Spastic; Physical medicine and rehabilitation; Pathology; Cerebral palsy; Disease; Phenotype; Psychiatry; Biology; Genetics","score_opus":0.032659922262067945,"score_gpt":0.28583407272914957,"score_spread":0.25317415046708164,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4307842001","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":[0.9984819,0.00047590333,0.0002862206,0.000029169394,0.0000024160481,0.00001037588,0.00021633082,0.000011964236,0.0004857888],"genre_scores_gemma":[0.9990086,0.00032141968,0.00025811433,0.000024993411,0.0000064112533,0.00000628355,0.0002509242,0.0000052134455,0.00011812275],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99977714,0.00003247138,0.0000297944,0.00008447291,0.000035152414,0.00004102004],"domain_scores_gemma":[0.9996817,0.000063864754,0.00013102911,0.00001789232,0.00003138392,0.000074130076],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0002891256,0.0006122972,0.0004086247,0.00075810344,0.00041506364,0.00029080836,0.00022911535,0.00030132942,0.0015291541],"category_scores_gemma":[0.00071989687,0.00012759738,0.00022188111,0.00049337285,0.00043451597,0.00027459968,0.0005931338,0.00019487462,0.00028863287],"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":[0.00032812293,0.000053910255,0.9107189,0.00011143088,0.00010198807,0.03672884,0.0010293551,0.00035166027,0.02734676,0.00020189326,0.000544985,0.022482218],"study_design_scores_gemma":[0.000007730981,0.00017764751,0.91826844,0.000034535165,0.00003705818,0.078959815,0.00029862527,0.00009168822,0.0012414178,0.00016729758,0.0007042376,0.000011574807],"about_ca_topic_score_codex":0.0010988011,"about_ca_topic_score_gemma":0.0014325686,"teacher_disagreement_score":0.0015291541,"about_ca_system_score_codex":0.00014087772,"about_ca_system_score_gemma":0.00015967271,"threshold_uncertainty_score":0.0051155686},"labels":[],"label_agreement":null},{"id":"W4308180501","doi":"10.1017/cjn.2022.318","title":"Ulnar Neuropathy with Silent Synapses","year":2022,"lang":"fr","type":"article","venue":"Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques","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":true,"route_about_ca":false,"ca_institutions":"University of Toronto","funders":"","keywords":"Content (measure theory); Ulnar nerve; Neuroscience; Medicine; Anatomy; Psychology; Mathematics","score_opus":0.037492072997386335,"score_gpt":0.25192557687805534,"score_spread":0.214433503880669,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4308180501","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":[0.9344671,0.0036542933,0.0045103203,0.0021451968,0.0005011259,0.0002520687,0.0010898369,0.0006318411,0.052748237],"genre_scores_gemma":[0.9873166,0.00081679504,0.00047837413,0.0007000998,0.0002789161,0.000029919718,0.00021522855,0.00003931575,0.010124801],"study_design_codex":"case_report","study_design_gemma":"case_report","domain_scores_codex":[0.9997094,0.00002793285,0.000029647126,0.00006530948,0.000055119854,0.00011249544],"domain_scores_gemma":[0.9991819,0.0002751913,0.00013411419,0.00012107141,0.000063770705,0.0002239454],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0002246765,0.0015998307,0.0007700403,0.0017309801,0.0013926525,0.0011039438,0.00095371256,0.0021156662,0.014750371],"category_scores_gemma":[0.0013963212,0.0004173315,0.0005194393,0.0012225308,0.0011472059,0.0013322276,0.0009157346,0.0016024787,0.0023608631],"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":[0.00044619586,0.00013799347,0.004413602,0.00019520536,0.000053605607,0.9787837,0.00012943213,0.00018023782,0.0026046862,0.0011084481,0.0015152693,0.010431574],"study_design_scores_gemma":[0.000114252514,0.0005798305,0.028399888,0.00009067774,0.00009830808,0.9638183,0.00019363244,0.0005039303,0.003054666,0.0019887788,0.0011183046,0.00003937954],"about_ca_topic_score_codex":0.0037750944,"about_ca_topic_score_gemma":0.0038916199,"teacher_disagreement_score":0.014750371,"about_ca_system_score_codex":0.000967126,"about_ca_system_score_gemma":0.00072634046,"threshold_uncertainty_score":0.049344897},"labels":[],"label_agreement":null},{"id":"W4308269670","doi":"10.1101/2022.11.04.515198","title":"Development of a novel oral treatment that rescues gait ataxia and retinal degeneration in a phenotypic mouse model of familial dysautonomia","year":2022,"lang":"en","type":"preprint","venue":"bioRxiv (Cold Spring Harbor Laboratory)","topic":"Hereditary Neurological Disorders","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 Institutes of Health; York University; Montana State University","keywords":"Ataxia; Retinal degeneration; RNA splicing; Phenotype; Biology; Exon; Alternative splicing; Degeneration (medical); Neuroscience; Cell biology; Gene; Genetics; Medicine; Pathology","score_opus":0.06682079940024713,"score_gpt":0.2495431226380935,"score_spread":0.18272232323784637,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4308269670","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":[0.99026185,0.0021224278,0.0047827368,0.00013225373,0.000051735817,0.00012704024,0.00058461,0.00021490536,0.0017225548],"genre_scores_gemma":[0.9886903,0.0017991534,0.004837717,0.000054338114,0.000011042554,0.00011828896,0.0006177723,0.000024018616,0.0038474197],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9999522,0.0000036816798,0.000003945901,0.000012445689,0.000015373593,0.000012389793],"domain_scores_gemma":[0.9999716,0.0000020842963,0.000008757775,0.0000024837132,0.0000045486586,0.000010546338],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00006157381,0.00031742224,0.00032766862,0.00029928517,0.00011978894,0.00014592879,0.0002153638,0.00031926506,0.0009669689],"category_scores_gemma":[0.00004212375,0.000088738234,0.00018799397,0.00010569168,0.00013832253,0.00013637767,0.00009075764,0.0004663166,0.00017481498],"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":[0.00017685618,0.00009638043,0.000091118534,0.000072501236,0.00000753725,0.000038589416,0.0000069101216,0.0000914797,0.9950658,0.00008027774,0.0000692238,0.0042032674],"study_design_scores_gemma":[0.0001563265,0.0034755813,0.0019147105,0.0000126029145,0.00006720339,0.00019692139,0.000016266202,0.00089305517,0.98789495,0.000037502334,0.0053257924,0.000009092477],"about_ca_topic_score_codex":0.00095773366,"about_ca_topic_score_gemma":0.0021026004,"teacher_disagreement_score":0.0009669689,"about_ca_system_score_codex":0.00022995201,"about_ca_system_score_gemma":0.00025813142,"threshold_uncertainty_score":0.0032348037},"labels":[],"label_agreement":null},{"id":"W4310044542","doi":"10.25259/sni_803_2022","title":"A novel single-point mutation of NEFH and biallelic SACS mutation presenting as intermediate form Charcot-Marie-Tooth: A case report in Vietnam","year":2022,"lang":"en","type":"article","venue":"Surgical Neurology International","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":1,"is_retracted":false,"has_abstract":true,"route_ca_aff":false,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":true,"ca_institutions":"","funders":"","keywords":"Missense mutation; Frameshift mutation; Sanger sequencing; Medicine; Genetics; Mutation; Compound heterozygosity; Exome sequencing; Ataxia; Gene; Biology","score_opus":0.03237910839985638,"score_gpt":0.28480209749009916,"score_spread":0.2524229890902428,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4310044542","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":[0.9952323,0.0008958499,0.0008139698,0.00041833657,0.00007136465,0.00006530378,0.00012996922,0.000037448553,0.0023354457],"genre_scores_gemma":[0.99778676,0.0005037781,0.00048496915,0.00020508209,0.000074816475,0.000011244642,0.000081693506,0.000017934355,0.0008337363],"study_design_codex":"case_report","study_design_gemma":"case_report","domain_scores_codex":[0.99940205,0.000043049622,0.00006971768,0.00023321483,0.00008257762,0.00016946672],"domain_scores_gemma":[0.998811,0.00022596816,0.00023364152,0.00007460137,0.00010358431,0.00055119843],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00024138649,0.0013784111,0.0011230017,0.0016449067,0.0020647144,0.0013598534,0.0010323889,0.0025795614,0.0025388158],"category_scores_gemma":[0.0014894556,0.0011784133,0.0008054709,0.00089158065,0.0014339965,0.0011731582,0.0013992984,0.0015274042,0.0004565267],"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":[0.000015657391,0.00002641065,0.0069498774,0.000027169197,0.0000106685675,0.9905399,0.00055624236,0.000024258576,0.0011698896,0.000062753206,0.000112636604,0.00050453364],"study_design_scores_gemma":[0.000007834525,0.000032902393,0.0049786996,0.000008903267,0.000008006322,0.99404883,0.00029484922,0.0000696128,0.00020783533,0.000048489277,0.00028669104,0.000007454454],"about_ca_topic_score_codex":0.006885261,"about_ca_topic_score_gemma":0.007272125,"teacher_disagreement_score":0.006885261,"about_ca_system_score_codex":0.0011267666,"about_ca_system_score_gemma":0.0009042011,"threshold_uncertainty_score":0.013690352},"labels":[],"label_agreement":null},{"id":"W4310154405","doi":"10.1007/s10072-022-06516-8","title":"Movement disorders in hereditary spastic paraplegia (HSP): a systematic review and individual participant data meta-analysis","year":2022,"lang":"en","type":"review","venue":"Neurological Sciences","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":17,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University Health Network; University of Toronto; Toronto Western Hospital; University of Ottawa","funders":"Karolinska Institutet","keywords":"Hereditary spastic paraplegia; Neurology; Meta-analysis; Movement disorders; Physical medicine and rehabilitation; Neuroradiology; Paraplegia; Spastic; Neurosurgery; Medicine; Psychology; Physical therapy; Neuroscience; Pathology; Psychiatry; Spinal cord; Cerebral palsy; Biology; Genetics","score_opus":0.5451055259071106,"score_gpt":0.410542020767941,"score_spread":0.1345635051391696,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4310154405","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":[0.009421809,0.9867194,0.0006839127,0.0002621368,0.00015826045,0.00040950283,0.0019837222,0.000032717748,0.00032850483],"genre_scores_gemma":[0.34616986,0.64254236,0.0032231808,0.0015598842,0.0002958836,0.0032107325,0.0025196054,0.000054559732,0.00042393478],"study_design_codex":"systematic_review","study_design_gemma":"meta_analysis","domain_scores_codex":[0.9845977,0.0073226495,0.00460527,0.0016902263,0.0013058105,0.00047842492],"domain_scores_gemma":[0.9613004,0.02963473,0.005490071,0.0011810631,0.002033002,0.00036069512],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.015784761,0.0019132657,0.016994238,0.0064035207,0.00070041005,0.0028204112,0.0022049567,0.0021646668,0.0040720324],"category_scores_gemma":[0.04224127,0.0012173082,0.026832612,0.009223125,0.0007516705,0.0017804175,0.0016020569,0.0013770465,0.00031646134],"study_design_candidate":"meta_analysis","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":[0.0012126614,0.000018352554,0.008598564,0.4999401,0.48164332,0.00015621525,0.00011440706,0.00035696576,0.0002098122,0.0001378809,0.00086109014,0.0067506353],"study_design_scores_gemma":[0.0006393916,0.00018532852,0.008956079,0.050405994,0.9370326,0.00015293431,0.00008556483,0.00018056588,0.000100820966,0.00020738516,0.0020246415,0.000028641116],"about_ca_topic_score_codex":0.006830758,"about_ca_topic_score_gemma":0.01571794,"teacher_disagreement_score":0.016994238,"about_ca_system_score_codex":0.0023589367,"about_ca_system_score_gemma":0.0036867862,"threshold_uncertainty_score":0.08347875},"labels":[],"label_agreement":null},{"id":"W4311034558","doi":"10.7759/cureus.32076","title":"Importance of Electrodiagnostic Testing Prior to a Tethered Cord Release in a Patient with Overlapping Symptoms of Charcot-Marie-Tooth Disease","year":2022,"lang":"en","type":"article","venue":"Cureus","topic":"Hereditary Neurological Disorders","field":"Neuroscience","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":"Cytodiagnostics (Canada)","funders":"","keywords":"Medicine; Weakness; Lumbar; Pes cavus; Ankle; Magnetic resonance imaging; Spinal cord; Urinary retention; Neurological examination; Urinary incontinence; Syringomyelia; Surgery; Radiology; Complication","score_opus":0.023799133363736198,"score_gpt":0.24450829430578788,"score_spread":0.22070916094205167,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4311034558","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":[0.968137,0.0063159238,0.0023298566,0.0070295795,0.00048184383,0.00013837258,0.0001847534,0.00019635019,0.015186388],"genre_scores_gemma":[0.9956885,0.00093672617,0.00069649826,0.0015463994,0.0004732754,0.000017975119,0.00011319291,0.000016197808,0.0005112498],"study_design_codex":"case_report","study_design_gemma":"case_report","domain_scores_codex":[0.9991665,0.00013503798,0.00013329225,0.00017934483,0.00015514401,0.00023061343],"domain_scores_gemma":[0.99764013,0.0010442467,0.00023685937,0.00009170613,0.00028436194,0.0007026531],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00045651582,0.0009193189,0.0010027818,0.0020611295,0.0012034327,0.0010602287,0.0009323619,0.003741437,0.0020444568],"category_scores_gemma":[0.004552601,0.00053932075,0.00067775266,0.0006549987,0.0008819775,0.0017336684,0.00067870645,0.002254671,0.00072785234],"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":[0.00015437158,0.00013151206,0.078085124,0.00005752941,0.000021376674,0.9138247,0.00044044427,0.00019148419,0.0022278288,0.00015668107,0.00083508936,0.0038737925],"study_design_scores_gemma":[0.000033438082,0.00026203197,0.058141395,0.00011446598,0.000040212042,0.93781585,0.00063586666,0.00081784755,0.0006412603,0.00022028551,0.0012395966,0.000037786205],"about_ca_topic_score_codex":0.0032340595,"about_ca_topic_score_gemma":0.0029474054,"teacher_disagreement_score":0.003741437,"about_ca_system_score_codex":0.00074959965,"about_ca_system_score_gemma":0.0006657267,"threshold_uncertainty_score":0.006839454},"labels":[],"label_agreement":null},{"id":"W4311095648","doi":"10.1007/978-1-0716-2651-1_1","title":"Introduction and Discovery of Retinitis Pigmentosa","year":2022,"lang":"en","type":"article","venue":"Methods in molecular biology","topic":"Hereditary Neurological Disorders","field":"Neuroscience","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":"Queen's University","funders":"National Eye Institute","keywords":"Retinitis pigmentosa; Blindness; Ophthalmology; Medicine; Optometry; Retinal","score_opus":0.0313858405278177,"score_gpt":0.36511959283380174,"score_spread":0.33373375230598407,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4311095648","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":[0.07261234,0.55245036,0.13428044,0.11829624,0.025022604,0.00033695908,0.0035187516,0.0015140134,0.09196836],"genre_scores_gemma":[0.37874487,0.30496567,0.16529872,0.030517459,0.022840347,0.0005934059,0.0022119847,0.00043107884,0.094396494],"study_design_codex":"theoretical_or_conceptual","study_design_gemma":"not_applicable","domain_scores_codex":[0.99914324,0.00023806293,0.000055719407,0.00025811067,0.00021701194,0.00008783391],"domain_scores_gemma":[0.99874336,0.00054700446,0.000109982306,0.00018436249,0.0002452728,0.00017006473],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.002018644,0.0005991397,0.00047022654,0.0020181397,0.00074529496,0.0018034333,0.0008993989,0.0020676856,0.0023134712],"category_scores_gemma":[0.0015926962,0.0005362288,0.0007261238,0.0006063146,0.0028420219,0.0019373475,0.0015602881,0.004029191,0.0010986102],"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":[0.0009914708,0.00020215444,0.002986528,0.0034079435,0.00010933875,0.0013891485,0.0010930294,0.0010097779,0.1534725,0.41566065,0.051700823,0.3679767],"study_design_scores_gemma":[0.000048047215,0.00016397261,0.001889131,0.0003571048,0.00004329769,0.0013521085,0.0001230992,0.0004226528,0.059515636,0.04272754,0.89330125,0.000056071036],"about_ca_topic_score_codex":0.0013096064,"about_ca_topic_score_gemma":0.0006758676,"teacher_disagreement_score":0.0023134712,"about_ca_system_score_codex":0.001695846,"about_ca_system_score_gemma":0.0010800199,"threshold_uncertainty_score":0.012304246},"labels":[],"label_agreement":null},{"id":"W4311693944","doi":"10.1093/pch/pxac098","title":"Living without pain. Case series of patients with hereditary sensory and autonomic neuropathies in a Canadian tertiary care centre","year":2022,"lang":"en","type":"article","venue":"Paediatrics & Child Health","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":3,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":true,"ca_institutions":"BC Children's Hospital; University of British Columbia","funders":"","keywords":"Medicine; Dysautonomia; Etiology; Pediatrics; Disease; Retrospective cohort study; Tertiary care; Internal medicine","score_opus":0.008215676145306538,"score_gpt":0.20670588135653414,"score_spread":0.1984902052112276,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4311693944","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":[0.99255073,0.0006192553,0.00012068199,0.00031952895,0.0000352747,0.000092785114,0.0004504742,0.000022379194,0.0057888557],"genre_scores_gemma":[0.9982774,0.00031958887,0.00025973126,0.00026566477,0.000030596715,0.000016238313,0.00026175438,0.00000720388,0.000561847],"study_design_codex":"observational","study_design_gemma":"case_report","domain_scores_codex":[0.99898726,0.000043571396,0.00007105136,0.00017355496,0.0002689944,0.00045548548],"domain_scores_gemma":[0.9984041,0.00010307884,0.0005317224,0.000050980303,0.0002480915,0.0006620577],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00024163378,0.0010725316,0.00040121932,0.0017283362,0.005249189,0.0009885799,0.0013204821,0.0010751104,0.0038753098],"category_scores_gemma":[0.0015616027,0.00060795137,0.00039564326,0.0029094343,0.0014315766,0.00035890404,0.0011932441,0.0009893333,0.0004120568],"study_design_candidate":"case_report","study_design_consensus":null,"about_ca_topic_candidate":true,"about_ca_topic_consensus":true,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.000070234564,0.00013725738,0.7744578,0.00009395923,0.000034485034,0.21283315,0.0026538523,0.00015728339,0.0013545693,0.00026018868,0.0019243362,0.006022912],"study_design_scores_gemma":[0.00002811862,0.00019764242,0.630532,0.000098399105,0.000039628318,0.36061138,0.0053786016,0.00029385946,0.00029968462,0.00010783544,0.0023669223,0.000045936133],"about_ca_topic_score_codex":0.6100216,"about_ca_topic_score_gemma":0.7445425,"teacher_disagreement_score":0.3899784,"about_ca_system_score_codex":0.009035321,"about_ca_system_score_gemma":0.0153326085,"threshold_uncertainty_score":0.78455013},"labels":[],"label_agreement":null},{"id":"W4311844243","doi":"10.7759/cureus.32296","title":"Heterogeneous Presentation of Hereditary Neuropathy With Liability to Pressure Palsies: Clinical and Electrodiagnostic Findings in Three Patients","year":2022,"lang":"en","type":"article","venue":"Cureus","topic":"Hereditary Neurological Disorders","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":false,"ca_institutions":"Cytodiagnostics (Canada)","funders":"","keywords":"Medicine; Foot drop; Entrapment Neuropathy; Genetic testing; Peripheral myelin protein 22; Polyradiculoneuropathy; Carpal tunnel syndrome; Multifocal motor neuropathy; Presentation (obstetrics); Surgery; Pediatrics; Internal medicine; Guillain-Barre syndrome","score_opus":0.02876254408614744,"score_gpt":0.2822219912427605,"score_spread":0.25345944715661306,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4311844243","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":[0.99877876,0.00014515272,0.00026912297,0.00006157369,0.000009120424,0.000031314874,0.00004756083,0.000012484166,0.00064485223],"genre_scores_gemma":[0.9994103,0.00008505341,0.0001954797,0.00007803184,0.000020245774,0.000016624015,0.00008440882,0.0000054343795,0.00010448337],"study_design_codex":"observational","study_design_gemma":"case_report","domain_scores_codex":[0.99951947,0.000055746656,0.00008865034,0.00012789217,0.00008290677,0.00012530421],"domain_scores_gemma":[0.99917644,0.00020353745,0.00019277321,0.000058557434,0.00008574703,0.00028300207],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0003074961,0.0012319988,0.00068726763,0.0012834631,0.0013675108,0.00087824446,0.0005931431,0.0010215805,0.0013703763],"category_scores_gemma":[0.0023639773,0.0005413077,0.00063812657,0.00086964865,0.0008278145,0.00056056894,0.0011316766,0.00056466693,0.00025313947],"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":[0.00034776272,0.00036845068,0.5263282,0.00006678521,0.00008137125,0.45584825,0.0025813852,0.00038189927,0.005708129,0.0002781562,0.0004303086,0.0075793816],"study_design_scores_gemma":[0.00006336492,0.0005636819,0.30797818,0.00003209016,0.00005918303,0.687467,0.0011281183,0.00049596746,0.0011677438,0.00022440916,0.00076157827,0.000058755406],"about_ca_topic_score_codex":0.0019612107,"about_ca_topic_score_gemma":0.0015235969,"teacher_disagreement_score":0.0019612107,"about_ca_system_score_codex":0.0006454099,"about_ca_system_score_gemma":0.00041388802,"threshold_uncertainty_score":0.004682839},"labels":[],"label_agreement":null},{"id":"W4313580744","doi":"10.4103/aian.aian_901_22","title":"Spastic paraplegia type 8: A first report from India","year":2023,"lang":"en","type":"article","venue":"Annals of Indian Academy of Neurology","topic":"Hereditary Neurological Disorders","field":"Neuroscience","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":"Spasticity; Medicine; Hereditary spastic paraplegia; Spastic; Urinary incontinence; Physical medicine and rehabilitation; Neurological examination; Paraplegia; Dysphagia; Physical therapy; Cerebral palsy; Surgery; Spinal cord","score_opus":0.1430913110057934,"score_gpt":0.3536573455574926,"score_spread":0.21056603455169923,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4313580744","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":[0.940896,0.026770053,0.0017761954,0.0057029207,0.0019070812,0.0003159739,0.0011291213,0.00024529512,0.02125724],"genre_scores_gemma":[0.9733334,0.015793953,0.00061202666,0.004295449,0.0024208548,0.000055114455,0.0006405806,0.00005560343,0.0027930061],"study_design_codex":"case_report","study_design_gemma":"case_report","domain_scores_codex":[0.999196,0.000060048304,0.00015525546,0.00021139019,0.00015099108,0.00022628348],"domain_scores_gemma":[0.998678,0.00025295856,0.0003017187,0.00012971861,0.00018264876,0.00045492413],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00021502403,0.0012253176,0.0010503342,0.003351726,0.0022443198,0.0014143633,0.0014913419,0.0035823206,0.0039177868],"category_scores_gemma":[0.0012998155,0.0009861308,0.0010568474,0.002835598,0.00093027315,0.0015953097,0.0015145823,0.0022740655,0.001798345],"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":[0.00010667289,0.00025221397,0.055252295,0.0004260365,0.000088025154,0.9204571,0.002470679,0.000112167814,0.0022562675,0.0003662647,0.006232372,0.011979792],"study_design_scores_gemma":[0.00001943425,0.0001615588,0.036230717,0.00013862191,0.00006062362,0.9535745,0.0010049167,0.000076089105,0.00019995886,0.00016753763,0.008311883,0.000054242988],"about_ca_topic_score_codex":0.005597925,"about_ca_topic_score_gemma":0.00666638,"teacher_disagreement_score":0.005597925,"about_ca_system_score_codex":0.0006364423,"about_ca_system_score_gemma":0.00095155835,"threshold_uncertainty_score":0.0131062865},"labels":[],"label_agreement":null},{"id":"W4318477704","doi":"10.3390/genes14020328","title":"Novel Variants in MPV17, PRX, GJB1, and SACS Cause Charcot–Marie–Tooth and Spastic Ataxia of Charlevoix–Saguenay Type Diseases","year":2023,"lang":"en","type":"article","venue":"Genes","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":15,"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":"King Abdulaziz University","keywords":"Sanger sequencing; Ataxia; Exome sequencing; Genetics; Medicine; Pes cavus; Founder effect; Spastic; Spasticity; Disease gene identification; Phenotype; Mutation; Biology; Internal medicine; Neuroscience; Genotype; Gene; Haplotype; Psychiatry","score_opus":0.05642104002658125,"score_gpt":0.27098337995668786,"score_spread":0.21456233993010662,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4318477704","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":[0.9987704,0.000208754,0.0002619701,0.000016017702,0.0000061183314,0.0000190609,0.00030735813,0.000010230956,0.00040009755],"genre_scores_gemma":[0.9984676,0.00015909501,0.0003898077,0.000020643758,0.000016102664,0.000018780516,0.00046535474,0.000007376655,0.00045514546],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9996544,0.00004598582,0.000045964076,0.00012494165,0.00006605798,0.00006267392],"domain_scores_gemma":[0.99970573,0.000085562526,0.00007563241,0.000024001354,0.000026839742,0.00008220577],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00022919553,0.0009468217,0.00045281003,0.00090636365,0.0006140252,0.00030431637,0.00035986956,0.00044402553,0.0024676768],"category_scores_gemma":[0.0007681326,0.00031738926,0.00031467696,0.0005526588,0.00045888513,0.00015264064,0.00047074404,0.00029017302,0.00036469122],"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":[0.0027115142,0.00041130433,0.7004485,0.00020872096,0.00025151114,0.15301889,0.0026851457,0.0005457936,0.1147428,0.00063026015,0.0015706634,0.022774914],"study_design_scores_gemma":[0.00022458934,0.0005522793,0.7873175,0.000043457658,0.00016776845,0.19493704,0.0005924162,0.00059755024,0.010887581,0.00020521553,0.0044387025,0.00003593892],"about_ca_topic_score_codex":0.0022140446,"about_ca_topic_score_gemma":0.0023596496,"teacher_disagreement_score":0.0024676768,"about_ca_system_score_codex":0.00028301263,"about_ca_system_score_gemma":0.00020795486,"threshold_uncertainty_score":0.008255124},"labels":[],"label_agreement":null},{"id":"W4318926634","doi":"10.1007/s10875-023-01440-8","title":"Autosomal Recessive Inflammatory Skin Disease Caused by a Novel Biallelic Loss-of-Function Variant in CARD11","year":2023,"lang":"en","type":"letter","venue":"Journal of Clinical Immunology","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":10,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"BC Children's Hospital; University of British Columbia","funders":"Canadian Institutes of Health Research; Uniformed Services University of the Health Sciences; Genome British Columbia; BC Children's Hospital; Children's Hospital Foundation; Jeffrey Modell Foundation; Killam Trusts; U.S. Department of Defense","keywords":"Loss function; Genetics; Medical microbiology; Disease; Biology; Function (biology); Medicine; Phenotype; Pathology; Gene; Immunology","score_opus":0.07863456936049096,"score_gpt":0.34335999857002353,"score_spread":0.26472542920953257,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4318926634","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":[0.9097953,0.0034865253,0.007001607,0.035051484,0.0047371206,0.00029416732,0.0009551504,0.00058973645,0.03808888],"genre_scores_gemma":[0.9866176,0.00050337,0.0019711321,0.004140551,0.0016777207,0.000037506103,0.00014310282,0.00005978319,0.004849065],"study_design_codex":"case_report","study_design_gemma":"case_report","domain_scores_codex":[0.9993875,0.00010615822,0.00006288304,0.00016113144,0.00010278379,0.00017945877],"domain_scores_gemma":[0.9985145,0.00072329474,0.0001950493,0.00007203416,0.00013875961,0.00035625353],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0004924233,0.0028453658,0.0009925951,0.0007739751,0.0014757273,0.0010434764,0.0012333955,0.0060765976,0.0035368623],"category_scores_gemma":[0.002848005,0.00038863978,0.0007418267,0.00066372106,0.0017083788,0.00080933236,0.00072233885,0.0029780157,0.0008360541],"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":[0.00022909213,0.00004079176,0.002567716,0.000033050972,0.000022435735,0.9886113,0.000078153826,0.00008079696,0.0040493,0.00075357215,0.0022631907,0.0012707134],"study_design_scores_gemma":[0.0002284285,0.00022088632,0.011072126,0.000049737144,0.000099226476,0.9799605,0.00015965842,0.0015639312,0.0025412212,0.0009385641,0.0031339657,0.0000317087],"about_ca_topic_score_codex":0.0018166059,"about_ca_topic_score_gemma":0.0017059839,"teacher_disagreement_score":0.0060765976,"about_ca_system_score_codex":0.00078896625,"about_ca_system_score_gemma":0.00071749865,"threshold_uncertainty_score":0.011831939},"labels":[],"label_agreement":null},{"id":"W4319993262","doi":"10.1016/j.pediatrneurol.2023.01.011","title":"The Spectrum of MORC2-Related Disorders: A Potential Link to Cockayne Syndrome","year":2023,"lang":"en","type":"article","venue":"Pediatric Neurology","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":17,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"McGill University; McGill University Health Centre","funders":"Fonds de Recherche du Québec - Santé; U.S. Food and Drug Administration; Canadian Institutes of Health Research; KWF Kankerbestrijding; Compute Canada; Oncode Institute; McGill University; Takeda Pharmaceuticals U.S.A.","keywords":"Cockayne syndrome; OMIM : Online Mendelian Inheritance in Man; Phenotype; Genetics; Biology; Microcephaly; DNA repair; Autism spectrum disorder; Nucleotide excision repair; Bioinformatics; Autism; Medicine; Gene; Psychiatry","score_opus":0.011594264136785798,"score_gpt":0.2354713913196583,"score_spread":0.2238771271828725,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4319993262","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":[0.97149235,0.0047175256,0.0024941312,0.0017179799,0.0000705945,0.000023074874,0.00029485123,0.00008635489,0.019103127],"genre_scores_gemma":[0.9973909,0.0006798829,0.0009594626,0.00015348269,0.000063717016,0.0000045495544,0.000071748706,0.000008528592,0.0006677219],"study_design_codex":"case_report","study_design_gemma":"observational","domain_scores_codex":[0.9998659,0.000017639557,0.000011081186,0.00003442005,0.000024946654,0.000046070356],"domain_scores_gemma":[0.9994667,0.00021618081,0.00013927113,0.0000270086,0.00004199947,0.00010878519],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00015126866,0.0005954547,0.00040990103,0.00128203,0.00074719865,0.00046180128,0.00050824106,0.0013966777,0.0061507616],"category_scores_gemma":[0.0008981905,0.00015696618,0.00021112488,0.0007305326,0.0008355054,0.00047213788,0.00057165365,0.00064971583,0.00035116432],"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":[0.0005968709,0.00012342833,0.11298914,0.00022624653,0.000118600845,0.76314217,0.0007074211,0.0009473344,0.08112784,0.012988945,0.0018393039,0.025192639],"study_design_scores_gemma":[0.00005979,0.00016747425,0.13577151,0.00017162245,0.0001373011,0.83148706,0.0006593769,0.0023072588,0.013368769,0.0077578463,0.008071786,0.00004016887],"about_ca_topic_score_codex":0.0023988318,"about_ca_topic_score_gemma":0.002815277,"teacher_disagreement_score":0.0061507616,"about_ca_system_score_codex":0.0004300743,"about_ca_system_score_gemma":0.00040974224,"threshold_uncertainty_score":0.020576298},"labels":[],"label_agreement":null},{"id":"W4321369966","doi":"10.1016/j.ajhg.2023.01.019","title":"Development of an oral treatment that rescues gait ataxia and retinal degeneration in a phenotypic mouse model of familial dysautonomia","year":2023,"lang":"en","type":"article","venue":"The American Journal of Human Genetics","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":17,"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; National Eye Institute; York University; Montana State University; National Institute of Neurological Disorders and Stroke; University of Tennessee; PTC Therapeutics; Massachusetts General Hospital","keywords":"Ataxia; Retinal degeneration; Biology; Phenotype; RNA splicing; Exon; Alternative splicing; Neuroscience; Degeneration (medical); Cell biology; Genetics; Medicine; Pathology; Gene; Retina","score_opus":0.09276632715526505,"score_gpt":0.30453601457374246,"score_spread":0.2117696874184774,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4321369966","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":[0.98861337,0.0026440164,0.0049515283,0.00019260445,0.00006781239,0.00016897934,0.0008807107,0.00028430286,0.0021966835],"genre_scores_gemma":[0.983827,0.0029434552,0.006326068,0.00008503373,0.0000140127595,0.00019466122,0.0011897756,0.000038628605,0.0053813234],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99992967,0.000005971429,0.0000062742765,0.000018818493,0.000021322929,0.000017868637],"domain_scores_gemma":[0.99995923,0.000003212898,0.000012863155,0.0000037040231,0.0000059160443,0.000015071459],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00008267073,0.0004151887,0.00040942145,0.00035045648,0.00014007682,0.00017319105,0.00027883507,0.00041966612,0.0010600287],"category_scores_gemma":[0.00005686625,0.0001292715,0.0002465046,0.00012204442,0.00017266735,0.00018249897,0.000107139924,0.0006286498,0.00022351948],"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":[0.00024174697,0.00013671788,0.000094705945,0.00008882024,0.000010489398,0.000053351006,0.00001019553,0.00011198886,0.99480045,0.00010232511,0.00009320869,0.0042559826],"study_design_scores_gemma":[0.00019169017,0.003949847,0.0020865817,0.000018607521,0.000083890714,0.0002428178,0.000019744517,0.0008041156,0.98631984,0.00004445907,0.006227018,0.000011486666],"about_ca_topic_score_codex":0.0011065692,"about_ca_topic_score_gemma":0.0024384672,"teacher_disagreement_score":0.0011065692,"about_ca_system_score_codex":0.00027265586,"about_ca_system_score_gemma":0.00032919034,"threshold_uncertainty_score":0.0035461783},"labels":[],"label_agreement":null},{"id":"W4323066978","doi":"10.1007/s00415-023-11643-z","title":"Neuromuscular junction involvement in inherited motor neuropathies: genetic heterogeneity and effect of oral salbutamol treatment","year":2023,"lang":"en","type":"article","venue":"Journal of Neurology","topic":"Hereditary Neurological Disorders","field":"Neuroscience","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":"Ottawa Hospital; Children's Hospital of Eastern Ontario; University of Ottawa","funders":"NIHR Cambridge Biomedical Research Centre; Addenbrooke's Charitable Trust, Cambridge University Hospitals; European Research Council; Medical Research Council; Canada Research Chairs; Department of Health and Social Care; Canadian Institutes of Health Research; Evelyn Trust; Lily Foundation; National Institute for Health and Care Research; Muscular Dystrophy Canada; Canada Foundation for Innovation; Newton Fund; Wellcome Trust","keywords":"Neuromuscular transmission; Neuromuscular junction; Salbutamol; Congenital myasthenic syndrome; Medicine; Repetitive nerve stimulation; Electromyography; Pyridostigmine; Multifocal motor neuropathy; Reinnervation; Neuroscience; Internal medicine; Myasthenia gravis; Acetylcholine receptor; Physical medicine and rehabilitation; Biology; Surgery; Mismatch negativity; Receptor","score_opus":0.036700657148046704,"score_gpt":0.2808239826447179,"score_spread":0.2441233254966712,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4323066978","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":[0.99818724,0.0012652676,0.000104388564,0.00002598459,0.0000024278959,0.000009637129,0.000040358413,0.0000053681993,0.000359391],"genre_scores_gemma":[0.99940777,0.00032060163,0.00013203267,0.000017648297,0.0000048107854,0.0000037290947,0.000052795018,0.0000018796828,0.000058872163],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.999814,0.00003064898,0.000030313122,0.000051405812,0.000048742924,0.00002499098],"domain_scores_gemma":[0.9996679,0.00011643678,0.0001333921,0.000013314456,0.000027509928,0.00004154949],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.000276214,0.00035437167,0.0005428624,0.0003546799,0.00016653587,0.00022662185,0.00019427964,0.000351324,0.00085259264],"category_scores_gemma":[0.00072675175,0.0000849988,0.00031556893,0.00026911148,0.0002952897,0.0001867943,0.00023775495,0.00017583743,0.000094828865],"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":[0.0032900886,0.00036329887,0.7099091,0.00035185582,0.0004847566,0.047284834,0.00042432887,0.000654209,0.17096195,0.00014298999,0.00013767759,0.06599495],"study_design_scores_gemma":[0.00007882525,0.001344448,0.96022654,0.000050897244,0.00016285363,0.033320766,0.00020347814,0.00038595402,0.0038663943,0.000080057485,0.00026678067,0.000012951872],"about_ca_topic_score_codex":0.0014032898,"about_ca_topic_score_gemma":0.00212697,"teacher_disagreement_score":0.0014032898,"about_ca_system_score_codex":0.0002964886,"about_ca_system_score_gemma":0.00020952779,"threshold_uncertainty_score":0.0028522015},"labels":[],"label_agreement":null},{"id":"W4362670955","doi":"10.3390/ijms24076808","title":"Microscopic and Biochemical Hallmarks of BICD2-Associated Muscle Pathology toward the Evaluation of Novel Variants","year":2023,"lang":"en","type":"article","venue":"International Journal of Molecular Sciences","topic":"Hereditary Neurological Disorders","field":"Neuroscience","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":"Children's Hospital of Eastern Ontario","funders":"European Regional Development Fund; Ministerium für Kultur und Wissenschaft des Landes Nordrhein-Westfalen; Westfälische Wilhelms-Universität Münster; Bundesministerium für Bildung und Forschung","keywords":"Pathology; Biology; Atrophy; Context (archaeology); Spinocerebellar ataxia; Spinal muscular atrophy; Neuroscience; Medicine; Ataxia; Disease","score_opus":0.09475208384982864,"score_gpt":0.35734719310956975,"score_spread":0.2625951092597411,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4362670955","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":[0.9961643,0.00069112424,0.0020120612,0.000049500333,0.000010146851,0.000015514403,0.00013158361,0.00003068587,0.0008951215],"genre_scores_gemma":[0.99680954,0.00024201606,0.0022394261,0.00003888024,0.0000072978182,0.000011188883,0.00017174508,0.000008807955,0.00047112218],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.999778,0.00003483969,0.000032909422,0.000078040226,0.000047430534,0.00002887962],"domain_scores_gemma":[0.9998099,0.000034262037,0.00004261914,0.000022690056,0.00004522287,0.000045324075],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00026292002,0.0005686144,0.00023480336,0.0011793891,0.0003498156,0.00029371007,0.0002562228,0.00044559373,0.0014426593],"category_scores_gemma":[0.00038528157,0.000207057,0.00020290162,0.00029437334,0.00060430204,0.00020385977,0.0006099714,0.00027185483,0.00025330848],"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":[0.00038076614,0.00004817047,0.08986722,0.00014380594,0.00006926057,0.022975435,0.00034713978,0.00020549745,0.8784967,0.00019405612,0.00014582295,0.0071261004],"study_design_scores_gemma":[0.00003644328,0.00047968092,0.47437498,0.000065800974,0.00016888222,0.28057927,0.00063519855,0.0024243435,0.23789132,0.0005640354,0.0027453313,0.000034743127],"about_ca_topic_score_codex":0.00056270615,"about_ca_topic_score_gemma":0.0010351395,"teacher_disagreement_score":0.0014426593,"about_ca_system_score_codex":0.0001804857,"about_ca_system_score_gemma":0.000114440474,"threshold_uncertainty_score":0.004826188},"labels":[],"label_agreement":null},{"id":"W4367840076","doi":"10.1523/jneurosci.1959-22.2023","title":"A New Mouse Model of Giant Axonal Neuropathy with Overt Phenotypes and Neurodegeneration Driven by Neurofilament Disorganization","year":2023,"lang":"en","type":"article","venue":"Journal of Neuroscience","topic":"Hereditary Neurological Disorders","field":"Neuroscience","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":"Université Laval; Centre Jeunesse de Quebec; Institut Universitaire en Santé Mentale de Québec","funders":"Canadian Institutes of Health Research; Government of Canada","keywords":"Neurodegeneration; Neurofilament; Neuroinflammation; Neuroscience; Genetically modified mouse; Peripherin; Knockout mouse; Pathogenesis; Biology; Amyotrophic lateral sclerosis; Phenotype; Disease; Transgene; Pathology; Medicine; Immunology; Gene; Genetics","score_opus":0.028311165225145696,"score_gpt":0.23330714125718646,"score_spread":0.20499597603204076,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4367840076","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":[0.96570224,0.0021312698,0.020883687,0.000943534,0.00031823965,0.00068194093,0.0036589305,0.0013826956,0.0042975796],"genre_scores_gemma":[0.8930346,0.0054513654,0.048119154,0.000811863,0.00020042119,0.0023176898,0.008415846,0.00040849324,0.04124059],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99946624,0.00005844764,0.00009366282,0.00016739518,0.0001189666,0.00009533425],"domain_scores_gemma":[0.9994404,0.00006417827,0.00020033488,0.000056717283,0.00005247713,0.00018603464],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00056593743,0.0026511173,0.0009701822,0.0021022942,0.00064618915,0.00063015334,0.0009937709,0.0020079862,0.0030616056],"category_scores_gemma":[0.0002368587,0.0008722371,0.00087427394,0.0006092574,0.0008745281,0.00097239524,0.00078037084,0.0026185862,0.0008157332],"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":[0.00039937472,0.00044661915,0.0003467858,0.00011965348,0.0000300448,0.000777622,0.00009184375,0.00015984035,0.9941368,0.00093345484,0.00032979905,0.0022281336],"study_design_scores_gemma":[0.0016141022,0.013530134,0.021248398,0.00032988153,0.00055019435,0.019369984,0.00040842372,0.00845988,0.8915425,0.0025454527,0.040213007,0.00018807722],"about_ca_topic_score_codex":0.000627624,"about_ca_topic_score_gemma":0.0012766874,"teacher_disagreement_score":0.0030616056,"about_ca_system_score_codex":0.00049380993,"about_ca_system_score_gemma":0.00040846656,"threshold_uncertainty_score":0.010242045},"labels":[],"label_agreement":null},{"id":"W4379185019","doi":"10.7759/cureus.39884","title":"Clinical Features of a Newly Described Mutation of Myelin Protein Zero in a Family","year":2023,"lang":"en","type":"article","venue":"Cureus","topic":"Hereditary Neurological Disorders","field":"Neuroscience","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":"Cytodiagnostics (Canada)","funders":"Invitae","keywords":"Medicine; Peripheral myelin protein 22; Gene duplication; Myelin; Disease; Mutation; Gene; Abnormality; Gene mutation; Pathology; Phenotype; Peripheral neuropathy; Genetics; Biology; Internal medicine; Endocrinology; Central nervous system","score_opus":0.09990899893561403,"score_gpt":0.3494705315381779,"score_spread":0.2495615326025639,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4379185019","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":[0.9922781,0.0007777286,0.00097388437,0.0005743015,0.00007683372,0.000050449802,0.00023198943,0.00007873225,0.0049579865],"genre_scores_gemma":[0.99614114,0.00038751317,0.00066008733,0.00023243482,0.0000771951,0.00002029603,0.00012107638,0.000015019054,0.0023452598],"study_design_codex":"case_report","study_design_gemma":"case_report","domain_scores_codex":[0.9997236,0.000027211177,0.000020691381,0.00011200557,0.000058980422,0.000057429275],"domain_scores_gemma":[0.9994548,0.00013702875,0.00007132516,0.000023696266,0.000056577155,0.00025650265],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00016455958,0.0014596991,0.00079446874,0.0012215031,0.0013786862,0.00039454873,0.000612768,0.0013493366,0.003127311],"category_scores_gemma":[0.0012446233,0.00040454665,0.00043668458,0.0005529254,0.000966043,0.000416428,0.00077294395,0.000745437,0.00042398603],"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":[0.00013214332,0.00018024544,0.029055282,0.00005815673,0.000045004585,0.9503416,0.0015422518,0.00017712587,0.010200071,0.0006357159,0.0011552052,0.0064772437],"study_design_scores_gemma":[0.000016160853,0.00016796723,0.030249858,0.000022020658,0.000034394157,0.96613276,0.00018874799,0.00022828515,0.0011573755,0.00020138313,0.0015772049,0.000023753557],"about_ca_topic_score_codex":0.003585176,"about_ca_topic_score_gemma":0.0033060326,"teacher_disagreement_score":0.003585176,"about_ca_system_score_codex":0.00053740776,"about_ca_system_score_gemma":0.00053950096,"threshold_uncertainty_score":0.010461867},"labels":[],"label_agreement":null},{"id":"W4379600435","doi":"10.1093/brain/awad187","title":"Genetic analysis and natural history of Charcot-Marie-Tooth disease CMTX1 due to <i>GJB1</i> variants","year":2023,"lang":"en","type":"article","venue":"Brain","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":35,"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 Health and Medical Research Council; Medical Research Council Canada; National Institute of Neurological Disorders and Stroke; National Institute for Health and Care Research; Argenx; Charcot-Marie-Tooth Association; University of Minnesota Foundation; Muscular Dystrophy Association; Sarepta Therapeutics; Ministero della Salute; Pfizer; Australian Government; University of Minnesota; Wayne State University; Mitsubishi Tanabe Pharma Corporation; Wellcome Trust; Alexion Pharmaceuticals; Medical Research Council; Biogen","keywords":"Missense mutation; Genotype; Disease; Phenotype; Genetic variants; Genetics; Internal medicine; Medicine; Longitudinal study; Biology; Gene; Pathology","score_opus":0.02090690669825359,"score_gpt":0.23845567388755895,"score_spread":0.21754876718930535,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4379600435","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":[0.99973947,0.000044553613,0.000025126526,0.000010056713,8.989363e-7,0.0000017929782,0.00006783334,0.000001312061,0.00010887623],"genre_scores_gemma":[0.9997398,0.000024112158,0.00003112597,0.0000080014215,0.0000035224912,0.0000027015424,0.00012851377,0.0000011142938,0.00006104342],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99968994,0.00006810858,0.000027991613,0.00010619905,0.000054192362,0.00005352061],"domain_scores_gemma":[0.99888605,0.00029437078,0.00043220547,0.00006323158,0.00008549792,0.00023866877],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00029832142,0.00021027109,0.00027315802,0.0006247164,0.00047396024,0.00037675299,0.0002797009,0.00040057767,0.00095155777],"category_scores_gemma":[0.0021684193,0.0001752003,0.00024450402,0.0005471449,0.0003604548,0.00029065754,0.00025142232,0.0003579982,0.00018360523],"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":[0.00024911767,0.00003553654,0.99568474,0.000003480428,0.000016665252,0.0014325434,0.00016260252,0.000082217535,0.0012717868,0.000026563122,0.00006228072,0.00097243587],"study_design_scores_gemma":[0.000008045253,0.0001935612,0.99465704,0.0000034836462,0.000011920349,0.004480218,0.00015629968,0.00022135548,0.0001415947,0.00003201626,0.00008888106,0.0000054868724],"about_ca_topic_score_codex":0.002569306,"about_ca_topic_score_gemma":0.0015239235,"teacher_disagreement_score":0.002569306,"about_ca_system_score_codex":0.00025862336,"about_ca_system_score_gemma":0.00015137008,"threshold_uncertainty_score":0.005108714},"labels":[],"label_agreement":null},{"id":"W4385075208","doi":"10.1002/mds.29524","title":"Plasma Neurofilament Light Chain Is Elevated in Adaptor Protein Complex <scp>4‐Related</scp> Hereditary Spastic Paraplegia","year":2023,"lang":"en","type":"article","venue":"Movement Disorders","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":11,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Hospital for Sick Children; University of Toronto; SickKids Foundation; University of Manitoba","funders":"Eunice Kennedy Shriver National Institute of Child Health and Human Development; National Institute of Neurological Disorders and Stroke; Manton Center for Orphan Disease Research, Boston Children's Hospital; Studienstiftung des Deutschen Volkes; Intellectual and Developmental Disabilities Research Center; Astellas Pharma; Deutsche Forschungsgemeinschaft; National Institutes of Health; University of Cambridge; Deutscher Akademischer Austauschdienst; Ministero della Salute; Spastic Paraplegia Foundation; International Parkinson and Movement Disorder Society; Biogen","keywords":"Signal transducing adaptor protein; Paraplegia; Hereditary spastic paraplegia; Spastic; Neuroscience; Medicine; Chemistry; Psychology; Physical medicine and rehabilitation; Internal medicine; Spinal cord; Biochemistry; Gene; Phenotype; Receptor","score_opus":0.03066037513331105,"score_gpt":0.24299597813525012,"score_spread":0.21233560300193907,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4385075208","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":[0.9996166,0.00007730996,0.00009320187,0.0000096895155,0.000001967257,0.000003183413,0.00006288625,0.0000062600316,0.00012886069],"genre_scores_gemma":[0.9996853,0.00002888168,0.00008555964,0.000011492853,0.0000049127775,0.0000035516991,0.00008936403,0.000001455925,0.00008950357],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9998209,0.00003295738,0.000020803353,0.00006205802,0.00003712622,0.000026254851],"domain_scores_gemma":[0.9995826,0.00006895201,0.00021617352,0.000018510353,0.00004011948,0.00007359866],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00015992444,0.00047039395,0.00035057543,0.0007136692,0.00032625752,0.00030214005,0.00015383704,0.00040755642,0.0018592222],"category_scores_gemma":[0.00068862084,0.00017871073,0.00017392781,0.00033933914,0.0003177777,0.00012376708,0.00027006402,0.00030639584,0.00020318545],"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":[0.003523688,0.00018020629,0.8311652,0.000132797,0.00029598805,0.008989797,0.00034448435,0.00020634662,0.14525041,0.00008986282,0.0004176844,0.0094034225],"study_design_scores_gemma":[0.000028643895,0.00038114103,0.98361915,0.000007894226,0.00007597998,0.010632972,0.00008097853,0.0003121475,0.0045849513,0.000052781495,0.00021753887,0.0000057749935],"about_ca_topic_score_codex":0.00096088095,"about_ca_topic_score_gemma":0.00069682475,"teacher_disagreement_score":0.0018592222,"about_ca_system_score_codex":0.00023979979,"about_ca_system_score_gemma":0.00009084562,"threshold_uncertainty_score":0.006219685},"labels":[],"label_agreement":null},{"id":"W4385210350","doi":"10.1212/wnl.0000000000207634","title":"Clinical Reasoning: A Septuagenarian With Painless Ulceration on the Fingertip","year":2023,"lang":"en","type":"article","venue":"Neurology","topic":"Hereditary Neurological Disorders","field":"Neuroscience","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":"Cytodiagnostics (Canada)","funders":"","keywords":"Presentation (obstetrics); Medicine; Amputation; Index finger; Index (typography); Surgery; Anatomy; Computer science","score_opus":0.08790910984272908,"score_gpt":0.31428210555212627,"score_spread":0.22637299570939717,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4385210350","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":[0.89606965,0.0048408173,0.0023899835,0.033375286,0.0014155789,0.00025989627,0.0003909545,0.000292742,0.060965065],"genre_scores_gemma":[0.9875617,0.0015402297,0.0009311993,0.004866544,0.0011330382,0.000025658219,0.00008342776,0.000019373712,0.003838777],"study_design_codex":"case_report","study_design_gemma":"case_report","domain_scores_codex":[0.9997533,0.000026433785,0.000039905222,0.00007105291,0.00003668225,0.00007259159],"domain_scores_gemma":[0.9995739,0.00013099985,0.00007607656,0.000021071692,0.000047048587,0.00015094882],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00026975703,0.0013085515,0.00047561873,0.00094647537,0.001605907,0.0007418109,0.00094862486,0.0028369036,0.003345232],"category_scores_gemma":[0.002468504,0.00034137297,0.0003199052,0.00059150055,0.0011671758,0.0011130511,0.00067747827,0.0016545604,0.00091539696],"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":[0.000038980845,0.000020668404,0.012070068,0.000025554928,0.000004721505,0.98300755,0.00045145946,0.0000723036,0.0005092091,0.00030388596,0.0019267763,0.001568752],"study_design_scores_gemma":[0.00001775839,0.00007795889,0.012184143,0.00007402563,0.000011679182,0.98328006,0.0005223066,0.00021461041,0.00026728545,0.0007045252,0.0026295746,0.000016007301],"about_ca_topic_score_codex":0.0041196565,"about_ca_topic_score_gemma":0.005888687,"teacher_disagreement_score":0.0041196565,"about_ca_system_score_codex":0.0008946246,"about_ca_system_score_gemma":0.00088648585,"threshold_uncertainty_score":0.011190891},"labels":[],"label_agreement":null},{"id":"W4385798659","doi":"10.1007/s00415-023-11918-5","title":"White matter abnormalities in 15 subjects with SPG76","year":2023,"lang":"en","type":"article","venue":"Journal of Neurology","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":1,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"McGill University Health Centre; McGill University; Montreal Neurological Institute and Hospital","funders":"Spastic Paraplegia Foundation","keywords":"White matter; Pathology; Abnormality; Grey matter; Proband; Atrophy; Medicine; Hyperintensity; Magnetic resonance imaging; Biology; Radiology; Mutation; Psychiatry","score_opus":0.029198717685059817,"score_gpt":0.25214226177965277,"score_spread":0.22294354409459294,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4385798659","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":[0.99920815,0.000086162494,0.000036071895,0.000011944996,0.0000037670998,0.0000110484525,0.000074483556,0.0000040916375,0.00056430465],"genre_scores_gemma":[0.99919945,0.00006266333,0.000057293884,0.000024904126,0.000009539468,0.000008957827,0.00015913951,0.000003810033,0.00047429177],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9997392,0.000030962143,0.000037507307,0.0000825776,0.000039397426,0.00007023947],"domain_scores_gemma":[0.99962807,0.000110424175,0.00007439749,0.000026499174,0.000061007508,0.00009960261],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00040140355,0.0013766919,0.00077196094,0.0024234636,0.0019760488,0.00070470676,0.0004095333,0.00081675407,0.003312374],"category_scores_gemma":[0.0012459215,0.000579343,0.00039001225,0.0012091461,0.0008860362,0.00052214693,0.0007792038,0.00041252334,0.0005141113],"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":[0.0019606242,0.0006229592,0.9291237,0.00006986223,0.00015712257,0.048630856,0.0027419853,0.00018692607,0.010433524,0.00014584053,0.00017847295,0.0057482123],"study_design_scores_gemma":[0.00006992841,0.0014839536,0.97634,0.000011596838,0.00013195397,0.018984554,0.0013237154,0.00015935901,0.00091389165,0.00016813328,0.00039723734,0.00001569411],"about_ca_topic_score_codex":0.01462673,"about_ca_topic_score_gemma":0.0089742895,"teacher_disagreement_score":0.01462673,"about_ca_system_score_codex":0.00045327214,"about_ca_system_score_gemma":0.0004425415,"threshold_uncertainty_score":0.029083192},"labels":[],"label_agreement":null},{"id":"W4386019396","doi":"10.1007/s00415-023-11862-4","title":"Analysis of muscle magnetic resonance imaging of a large cohort of patient with VCP-mediated disease reveals characteristic features useful for diagnosis","year":2023,"lang":"en","type":"article","venue":"Journal of Neurology","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":12,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Ottawa Hospital","funders":"Muscular Dystrophy UK; National Center of Neurology and Psychiatry; Medical Research Council; AFM-Téléthon; National Institute for Health and Care Research; Academy of Medical Sciences","keywords":"Magnetic resonance imaging; Neuroradiology; Neurology; Medicine; Disease; Cohort; Muscle disease; Radiology; Pathology; Nuclear magnetic resonance; Physics; Psychiatry","score_opus":0.014621010269497792,"score_gpt":0.2586372182176093,"score_spread":0.24401620794811152,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4386019396","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":[0.99962914,0.00007614827,0.00006368831,0.0000079567,0.000001372046,0.0000045120205,0.0000545294,0.0000031224208,0.0001594535],"genre_scores_gemma":[0.9996451,0.000042518346,0.00010295532,0.000011808945,0.000006110948,0.000004885328,0.00013677019,0.0000017033065,0.000048131238],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9998374,0.00001907355,0.000018015899,0.00006350045,0.000034917768,0.000027086055],"domain_scores_gemma":[0.999637,0.00009608125,0.00010736142,0.000026261765,0.00004328149,0.00008995586],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00026171203,0.0003610603,0.00029097198,0.00079900475,0.0003127303,0.00032600752,0.00019714593,0.00034101485,0.0010343244],"category_scores_gemma":[0.0010325576,0.00011751936,0.00017511728,0.00032847497,0.0002704655,0.00023060938,0.0002608526,0.00022712868,0.00020341997],"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":[0.00012415324,0.000041002353,0.9829935,0.000012816388,0.000031531934,0.0028087767,0.00010145413,0.0000539391,0.010870704,0.000015759511,0.000105727646,0.002840731],"study_design_scores_gemma":[0.0000085137435,0.00018196713,0.98667836,0.000006637716,0.0000308971,0.011360166,0.00012377818,0.0001837595,0.0012033131,0.000021862777,0.00019643221,0.000004416476],"about_ca_topic_score_codex":0.0006763886,"about_ca_topic_score_gemma":0.0008001484,"teacher_disagreement_score":0.0010343244,"about_ca_system_score_codex":0.00015835193,"about_ca_system_score_gemma":0.0001435302,"threshold_uncertainty_score":0.0034601688},"labels":[],"label_agreement":null},{"id":"W4386516702","doi":"10.1177/19418744231190143","title":"Parakinesia Brachialis Oscitans and Excessive yawning From Tumefactive Demyelination","year":2023,"lang":"en","type":"article","venue":"The Neurohospitalist","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":2,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of British Columbia","funders":"","keywords":"Medicine; Brachialis; Internal capsule; Brainstem; Multiple sclerosis; Pathology; Magnetic resonance imaging; Radiology; White matter; Psychiatry","score_opus":0.03352717113896594,"score_gpt":0.2623590515238953,"score_spread":0.22883188038492938,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4386516702","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":[0.9846601,0.0029837824,0.0017219109,0.00077573385,0.00012734682,0.00009221319,0.00013072795,0.000106113046,0.0094021],"genre_scores_gemma":[0.99746704,0.0006643491,0.00044953052,0.00024568508,0.00015886815,0.0000119558135,0.0000398352,0.000007924861,0.0009547765],"study_design_codex":"case_report","study_design_gemma":"case_report","domain_scores_codex":[0.99982834,0.000018679773,0.00001687968,0.000037551705,0.000022938068,0.000075644144],"domain_scores_gemma":[0.9995679,0.00010508349,0.00014304157,0.00003515203,0.000021258007,0.00012757955],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00012571852,0.0011727805,0.0004983083,0.0010293988,0.00074450386,0.00054854824,0.00031339767,0.0014973326,0.0016871394],"category_scores_gemma":[0.0010170887,0.00044916812,0.0002989612,0.00056956033,0.0007564544,0.000791533,0.0007825113,0.0014035659,0.00047415996],"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":[0.00007439449,0.000025603465,0.008025818,0.000038907485,0.000007253,0.9873301,0.00017819984,0.0000735324,0.002003395,0.00019366188,0.00010998704,0.0019391879],"study_design_scores_gemma":[0.000018133665,0.00009165035,0.013845258,0.000013512523,0.0000109893335,0.98417675,0.00010111773,0.00018329483,0.00082698924,0.00020423578,0.0005169696,0.000011085077],"about_ca_topic_score_codex":0.0023361002,"about_ca_topic_score_gemma":0.0028582176,"teacher_disagreement_score":0.0023361002,"about_ca_system_score_codex":0.0004555108,"about_ca_system_score_gemma":0.000387391,"threshold_uncertainty_score":0.0056440234},"labels":[],"label_agreement":null},{"id":"W4387221518","doi":"10.1101/2023.09.28.559870","title":"Transcriptome analysis in a humanized mouse model of familial dysautonomia reveals tissue-specific gene expression disruption in the peripheral nervous system","year":2023,"lang":"en","type":"preprint","venue":"bioRxiv (Cold Spring Harbor Laboratory)","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":0,"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; York University; PTC Therapeutics; Massachusetts General Hospital","keywords":"Biology; Transcriptome; Gene; Dorsal root ganglion; Phenotype; Genetics; Neuroscience; Cell biology; Gene expression; Spinal cord","score_opus":0.05044656336121727,"score_gpt":0.2533264027258602,"score_spread":0.20287983936464293,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4387221518","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":[0.98981196,0.0008097386,0.0049697533,0.000087619905,0.00003787039,0.000039083297,0.00347475,0.00014317209,0.0006259646],"genre_scores_gemma":[0.9772943,0.001449414,0.008709643,0.00017733847,0.000012448763,0.00019560101,0.0061443523,0.00009580388,0.0059209727],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9997814,0.000010667607,0.000017102087,0.00009811771,0.000057865822,0.000034775112],"domain_scores_gemma":[0.99990165,0.0000114295335,0.000035707064,0.000010320427,0.000012411896,0.000028398868],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00010798035,0.0003814797,0.0002946429,0.00060137577,0.00020959793,0.00029146203,0.00015730706,0.00034660567,0.0010016822],"category_scores_gemma":[0.00008420929,0.00019788303,0.00040713392,0.00033390816,0.00030207238,0.00014690204,0.0001789341,0.00064303045,0.00031176457],"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":[0.000093677234,0.000013823692,0.00025144295,0.00001783755,0.0000057719494,0.000057811747,0.0000144630985,0.000032929747,0.9990729,0.00002771963,0.000025272224,0.00038626348],"study_design_scores_gemma":[0.00005256995,0.00071266096,0.054919887,0.000028806946,0.00014328041,0.001724217,0.00022713674,0.0026271658,0.93489,0.00018818359,0.0044649635,0.000021097592],"about_ca_topic_score_codex":0.00077233283,"about_ca_topic_score_gemma":0.0013150558,"teacher_disagreement_score":0.0010016822,"about_ca_system_score_codex":0.00024394189,"about_ca_system_score_gemma":0.00019345172,"threshold_uncertainty_score":0.0033509731},"labels":[],"label_agreement":null},{"id":"W4387302936","doi":"10.1016/j.nmd.2023.07.048","title":"P67 Novel therapeutic approaches in inherited neuropathies: a systematic review","year":2023,"lang":"en","type":"review","venue":"Neuromuscular Disorders","topic":"Hereditary Neurological Disorders","field":"Neuroscience","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":"Hospital for Sick Children","funders":"","keywords":"Medicine","score_opus":0.26717033189692774,"score_gpt":0.3421935797943267,"score_spread":0.07502324789739895,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4387302936","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":[0.000095273776,0.99955934,0.000037292495,0.000056914123,0.00004560887,0.000012842472,0.000043232583,0.0000022567062,0.00014715719],"genre_scores_gemma":[0.0006768152,0.9989507,0.00009343443,0.00013309023,0.000036895315,0.000013958641,0.000036037716,8.3706726e-7,0.00005819757],"study_design_codex":"design_other","study_design_gemma":"systematic_review","domain_scores_codex":[0.9995209,0.00010658417,0.00015920635,0.00007405852,0.00010479044,0.000034578534],"domain_scores_gemma":[0.9986557,0.00093758164,0.00022148366,0.000020769005,0.00012747139,0.000036969956],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0013333489,0.001134397,0.004011156,0.0032977203,0.0003022755,0.001469578,0.0014199284,0.0013593044,0.0058692936],"category_scores_gemma":[0.0032144655,0.00038969523,0.0029309206,0.0030587006,0.00040096638,0.0011635232,0.00089611334,0.0012672625,0.00067224394],"study_design_candidate":"systematic_review","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0005724235,0.00007560442,0.00031189248,0.45769894,0.0036264483,0.00025124033,0.00009447065,0.00038938253,0.00069535535,0.0007693594,0.013223865,0.52229106],"study_design_scores_gemma":[0.0014543995,0.0007979635,0.004812359,0.48430824,0.053701207,0.0024045818,0.00038114263,0.00033708697,0.0007299593,0.0020977615,0.4488388,0.00013656272],"about_ca_topic_score_codex":0.0026307378,"about_ca_topic_score_gemma":0.00893022,"teacher_disagreement_score":0.0058692936,"about_ca_system_score_codex":0.0008121379,"about_ca_system_score_gemma":0.0022589131,"threshold_uncertainty_score":0.019634783},"labels":[],"label_agreement":null},{"id":"W4387780900","doi":"10.3389/fdmed.2023.1179795","title":"Case report: Hereditary sensory autonomic neuropathy presenting as bifid deformity to the tongue","year":2023,"lang":"en","type":"article","venue":"Frontiers in Dental Medicine","topic":"Hereditary Neurological Disorders","field":"Neuroscience","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","funders":"","keywords":"Medicine; Tongue; Enucleation; Disfigurement; Deformity; Surgery; Pathology","score_opus":0.03816962951301123,"score_gpt":0.2877722881562163,"score_spread":0.24960265864320508,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4387780900","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":[0.96459097,0.008149038,0.0043423623,0.004141386,0.0008079647,0.00030444574,0.00059941114,0.00024844415,0.016815968],"genre_scores_gemma":[0.9915047,0.0021507652,0.0020802685,0.0010465172,0.00064396317,0.00004538391,0.00014257053,0.0000287495,0.0023570498],"study_design_codex":"case_report","study_design_gemma":"case_report","domain_scores_codex":[0.9994117,0.00004076323,0.0000708524,0.00018663151,0.00009060327,0.0001995232],"domain_scores_gemma":[0.9992416,0.00018055846,0.00018073729,0.00006496225,0.00005975615,0.00027243866],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00022914507,0.0020944334,0.0015459139,0.0023611,0.0033975954,0.0017360655,0.0012393396,0.005392914,0.0031074171],"category_scores_gemma":[0.0019565513,0.00094148866,0.0011954614,0.0016286946,0.0016997617,0.0019116619,0.0019517081,0.0035687385,0.0007597731],"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":[0.000011612883,0.000021215224,0.0018313644,0.000013730459,0.0000041616913,0.9966472,0.00012448408,0.000039366325,0.00031981425,0.00011599187,0.00013717587,0.0007338628],"study_design_scores_gemma":[0.0000033375106,0.000016852007,0.0010031271,0.000010491968,0.0000039465094,0.9983644,0.00009226467,0.00006151137,0.00012848477,0.000092853974,0.00021736308,0.0000053902127],"about_ca_topic_score_codex":0.0047696237,"about_ca_topic_score_gemma":0.005684012,"teacher_disagreement_score":0.005392914,"about_ca_system_score_codex":0.0019067291,"about_ca_system_score_gemma":0.0010857587,"threshold_uncertainty_score":0.013834298},"labels":[],"label_agreement":null},{"id":"W4388216014","doi":"10.1136/jnnp-2023-332422","title":"Use, tolerability, benefits and side effects of orthotic devices in Charcot-Marie-Tooth disease","year":2023,"lang":"en","type":"article","venue":"Journal of Neurology Neurosurgery & Psychiatry","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":10,"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":"Ministero della Salute","keywords":"Tolerability; Medicine; Physical therapy; Distress; Orthopedic surgery; Surgery; Internal medicine; Adverse effect","score_opus":0.034088816887792694,"score_gpt":0.26059997749607156,"score_spread":0.22651116060827886,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4388216014","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":[0.99866724,0.0009075692,0.0000363834,0.000019685034,0.0000018305325,0.000010091077,0.00011400209,0.0000015857205,0.0002416764],"genre_scores_gemma":[0.99926144,0.00039437853,0.000084032836,0.000016161992,0.0000058595347,0.000008799829,0.00013701229,7.030513e-7,0.00009162944],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9990963,0.0003315265,0.0001193303,0.00007476015,0.0002933176,0.000084774554],"domain_scores_gemma":[0.99704534,0.0009943265,0.0014724528,0.00006589324,0.0002113214,0.00021069836],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0013714476,0.00022230927,0.00029978008,0.000594276,0.00020983788,0.0003492829,0.00015936348,0.00024159094,0.0011833863],"category_scores_gemma":[0.002957402,0.00009951486,0.00042397834,0.0007551915,0.00023140914,0.00019103836,0.00022041124,0.00024774706,0.00014081862],"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":[0.0012024095,0.0001761826,0.9845697,0.00016928973,0.000077836106,0.0002986499,0.00026812934,0.000106176594,0.0007783589,0.000005423955,0.00008094748,0.012266956],"study_design_scores_gemma":[0.000016933509,0.0011408704,0.9974642,0.000021833279,0.000049829345,0.0007713367,0.00015493509,0.00009821233,0.00013079547,0.000006341691,0.00013909061,0.0000056179924],"about_ca_topic_score_codex":0.003160781,"about_ca_topic_score_gemma":0.004873789,"teacher_disagreement_score":0.003160781,"about_ca_system_score_codex":0.00047152842,"about_ca_system_score_gemma":0.0002336354,"threshold_uncertainty_score":0.007252991},"labels":[],"label_agreement":null},{"id":"W4388824117","doi":"10.1097/wno.0000000000002039","title":"Spastic Paraplegia Type 7-Associated Optic Neuropathy: A Case Series","year":2023,"lang":"en","type":"article","venue":"Journal of Neuro-Ophthalmology","topic":"Hereditary Neurological Disorders","field":"Neuroscience","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":"Western University","funders":"","keywords":"Medicine; Optic neuropathy; Atrophy; Hereditary spastic paraplegia; Genetic testing; Peripheral neuropathy; Ophthalmology; Visual acuity; Pediatrics; Optic nerve; Pathology; Internal medicine; Diabetes mellitus; Phenotype","score_opus":0.07567749640732903,"score_gpt":0.31024657171297576,"score_spread":0.23456907530564675,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4388824117","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":[0.9938438,0.0023406378,0.0007851089,0.00020021795,0.00009243661,0.00012134525,0.00010205147,0.000039702234,0.002474696],"genre_scores_gemma":[0.99810326,0.00069879164,0.0003418169,0.00017529336,0.00019757541,0.00003523716,0.00011252956,0.000009081225,0.00032629992],"study_design_codex":"case_report","study_design_gemma":"case_report","domain_scores_codex":[0.99899524,0.00009496871,0.00017185365,0.0002572213,0.00018591773,0.00029478563],"domain_scores_gemma":[0.99851245,0.00030336218,0.00045546357,0.00015473228,0.0001380484,0.0004359347],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00041342704,0.0015848051,0.00091167766,0.002009378,0.0021424284,0.0015299969,0.0011076271,0.002193191,0.0024688155],"category_scores_gemma":[0.002435531,0.00092999707,0.0010490083,0.0014725688,0.0014550774,0.0009969268,0.0014870528,0.0010845709,0.0008993602],"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":[0.00009909883,0.00027165393,0.13819174,0.00011318618,0.000105024585,0.85260636,0.0008123662,0.0001119101,0.0012899896,0.00014410641,0.000789326,0.0054652207],"study_design_scores_gemma":[0.000036523135,0.00020854571,0.0471906,0.00003818182,0.00005370607,0.9507432,0.00040265208,0.00020612119,0.00028634619,0.00008750898,0.00072707114,0.00001959927],"about_ca_topic_score_codex":0.0020790691,"about_ca_topic_score_gemma":0.0032608914,"teacher_disagreement_score":0.0024688155,"about_ca_system_score_codex":0.0009089837,"about_ca_system_score_gemma":0.0008122362,"threshold_uncertainty_score":0.008259058},"labels":[],"label_agreement":null},{"id":"W4388828510","doi":"10.1177/2050313x231213137","title":"A case of erythromelalgia with gastrointestinal dysautonomia treated with immunoglobulin: A case report","year":2023,"lang":"en","type":"article","venue":"SAGE Open Medical Case Reports","topic":"Hereditary Neurological Disorders","field":"Neuroscience","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":"Public Health Ontario; McMaster University; University of Toronto; Queen's University","funders":"","keywords":"Medicine; Dysautonomia; Erythromelalgia; Dermatology; Immunoglobulin E; Intravenous Immunoglobulin Therapy; Hyperhidrosis; Eosinophilic esophagitis; Antibody; Gastroenterology; Immunology; Internal medicine; Disease","score_opus":0.03482823162328061,"score_gpt":0.29712815877605153,"score_spread":0.26229992715277095,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4388828510","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":[0.9571025,0.013221862,0.0052841315,0.00442479,0.0008129754,0.00029652545,0.0002462487,0.00028410493,0.018326977],"genre_scores_gemma":[0.9901495,0.002565092,0.0020208657,0.0014314563,0.0016802137,0.000055178687,0.00009031952,0.000029169221,0.0019781224],"study_design_codex":"case_report","study_design_gemma":"case_report","domain_scores_codex":[0.99914634,0.000102242666,0.000089290996,0.00020269123,0.00010371953,0.00035558327],"domain_scores_gemma":[0.99871457,0.0003574815,0.00027952448,0.0001526123,0.00008487205,0.000410981],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00042182917,0.0031111166,0.0015582644,0.0030155326,0.0044962107,0.0022695335,0.0019400406,0.0083316285,0.002260517],"category_scores_gemma":[0.0027256282,0.001730536,0.002016734,0.0023909665,0.00225674,0.0027606466,0.0023946008,0.0047008996,0.0012205098],"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":[0.000008349195,0.00002601145,0.001221681,0.000009971849,0.0000043727027,0.9980457,0.000066353045,0.000018956986,0.00017344381,0.000058392292,0.00006695808,0.00029997196],"study_design_scores_gemma":[0.0000075888247,0.000022970291,0.00094910635,0.0000063185234,0.000009468046,0.9984962,0.000055589302,0.000084247375,0.000108860986,0.00006160849,0.00019281953,0.000005305883],"about_ca_topic_score_codex":0.0025186315,"about_ca_topic_score_gemma":0.0030606873,"teacher_disagreement_score":0.0083316285,"about_ca_system_score_codex":0.0016600988,"about_ca_system_score_gemma":0.00095205347,"threshold_uncertainty_score":0.012044907},"labels":[],"label_agreement":null},{"id":"W4389132384","doi":"10.1007/s00223-023-01164-2","title":"The Relationship Between Scoliosis, Spinal Bone Density, and Truncal Muscle Strength in Familial Dysautonomia Patients","year":2023,"lang":"en","type":"article","venue":"Calcified Tissue International","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":3,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"McGill University","funders":"","keywords":"Medicine; Scoliosis; Osteoporosis; Bone mineral; Familial dysautonomia; Orthopedic surgery; Lumbar; Physical therapy; Internal medicine; Surgery","score_opus":0.07032599577190017,"score_gpt":0.32385722956781887,"score_spread":0.2535312337959187,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4389132384","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":[0.99938536,0.00013840108,0.00002156827,0.000030455147,0.0000022234199,0.0000014174667,0.00006985728,0.000002471462,0.0003481862],"genre_scores_gemma":[0.99980134,0.00003145168,0.000022984044,0.000008543971,0.0000035508685,0.0000014006954,0.000056026238,8.8245e-7,0.000073728166],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99975866,0.000055456814,0.00004352743,0.000057048353,0.000043209544,0.000042120293],"domain_scores_gemma":[0.998958,0.00037348393,0.00031702884,0.00003626767,0.000078430705,0.00023679846],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00024383399,0.00043907107,0.00039737046,0.0013688249,0.0008079235,0.00053813535,0.0003556798,0.0007567245,0.0020802577],"category_scores_gemma":[0.002020073,0.00027527256,0.00031369,0.0010514581,0.00044113223,0.00032887916,0.00032551808,0.00041003077,0.00017121594],"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":[0.0002272388,0.000033590237,0.9965861,0.000006656529,0.000054186945,0.0012399383,0.000117846765,0.000065298635,0.0007069633,0.00002835506,0.00005041289,0.0008833494],"study_design_scores_gemma":[0.000006823915,0.00006462913,0.99719596,0.0000032448002,0.000030822586,0.0022433451,0.00014436952,0.0001623814,0.000060373597,0.00004088621,0.000043161468,0.0000040094615],"about_ca_topic_score_codex":0.008513215,"about_ca_topic_score_gemma":0.008068412,"teacher_disagreement_score":0.008513215,"about_ca_system_score_codex":0.00040791227,"about_ca_system_score_gemma":0.00029741722,"threshold_uncertainty_score":0.016927302},"labels":[],"label_agreement":null},{"id":"W4389436381","doi":"10.1212/wnl.90.15_supplement.p6.039","title":"CAPN1: novel mutations expanding the phenotype of hereditary spastic paraparesis. (P6.039)","year":2018,"lang":"en","type":"article","venue":"Neurology","topic":"Hereditary Neurological Disorders","field":"Neuroscience","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; University of Alberta","funders":"","keywords":"Phenotype; Genetics; Medicine; Neurogenetics; Mutation; Biology; Gene","score_opus":0.05096532712356879,"score_gpt":0.28631862722984125,"score_spread":0.23535330010627245,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4389436381","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":[0.9787133,0.0019253514,0.002909797,0.0012504694,0.0002191094,0.0002144393,0.0028381255,0.00013515851,0.011794191],"genre_scores_gemma":[0.9901778,0.00045208432,0.004164236,0.00043206097,0.00009015463,0.00008059766,0.0015071109,0.000038681028,0.0030572056],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9998945,0.000010910199,0.000010836596,0.000029684841,0.000033076067,0.000021045047],"domain_scores_gemma":[0.9998816,0.000018887458,0.000025178846,0.000005649559,0.000021933793,0.000046771253],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00012280847,0.0005146703,0.00029412872,0.00038730513,0.00035221758,0.00021228778,0.00041242564,0.0008337744,0.0038047237],"category_scores_gemma":[0.00029685887,0.000087596505,0.00025834388,0.00036784302,0.00019630014,0.00019666622,0.00028192974,0.00037256896,0.0011818778],"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":[0.002720781,0.0012520431,0.0498565,0.0005588488,0.00007380945,0.17466512,0.00056533015,0.0012096643,0.6482053,0.0022869837,0.014730124,0.103875555],"study_design_scores_gemma":[0.00057230773,0.0019390977,0.21313474,0.00013817669,0.00013241479,0.53069806,0.0002759114,0.003120086,0.20019181,0.002009474,0.04770578,0.00008212426],"about_ca_topic_score_codex":0.0011047197,"about_ca_topic_score_gemma":0.0013727497,"teacher_disagreement_score":0.0038047237,"about_ca_system_score_codex":0.0003398735,"about_ca_system_score_gemma":0.00021770087,"threshold_uncertainty_score":0.012728035},"labels":[],"label_agreement":null},{"id":"W4389450187","doi":"10.1212/wnl.94.15_supplement.4183","title":"A New Case Of Spastic Paraplegia Type 64 Due To A Missense Mutation In The ENTPD1 Gene (4183)","year":2020,"lang":"en","type":"article","venue":"Neurology","topic":"Hereditary Neurological Disorders","field":"Neuroscience","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":"Dr. Georges-L.-Dumont University Hospital Centre","funders":"","keywords":"Missense mutation; Mutation; Spastic; Hereditary spastic paraplegia; Paraplegia; Medicine; Gene; Genetics; Biology; Phenotype; Physical medicine and rehabilitation; Spinal cord; Cerebral palsy","score_opus":0.054337872483104024,"score_gpt":0.2825140254701427,"score_spread":0.2281761529870387,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4389450187","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":[0.9896667,0.0010916934,0.0011033511,0.0013084327,0.0002314228,0.00006422269,0.00021213616,0.00010815426,0.0062138312],"genre_scores_gemma":[0.99498194,0.00047942984,0.0006996817,0.00053991925,0.00021270511,0.000020376008,0.00011874056,0.000025014686,0.002922266],"study_design_codex":"case_report","study_design_gemma":"case_report","domain_scores_codex":[0.99967647,0.00002405707,0.00004081527,0.00008846882,0.0000506533,0.00011959789],"domain_scores_gemma":[0.99918205,0.00017527628,0.00018180485,0.00010290624,0.000054211232,0.00030378366],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00023916729,0.0015578624,0.0008136263,0.0019519159,0.0016481213,0.0007173127,0.000808357,0.003223425,0.0030439296],"category_scores_gemma":[0.0016642864,0.0011253147,0.0010661584,0.0014085887,0.001219299,0.0007688639,0.001281136,0.0016625664,0.00079750165],"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":[0.00003898072,0.000034218636,0.0027387678,0.000014939979,0.000010498164,0.994402,0.00009689239,0.000039120074,0.0014159215,0.00007403508,0.00020067993,0.0009340289],"study_design_scores_gemma":[0.000027359718,0.00008745321,0.011113813,0.000008101072,0.000020340454,0.9873855,0.00005519599,0.00012250672,0.00043197916,0.00020971773,0.0005258116,0.000012145179],"about_ca_topic_score_codex":0.004201364,"about_ca_topic_score_gemma":0.0041588857,"teacher_disagreement_score":0.004201364,"about_ca_system_score_codex":0.00077216583,"about_ca_system_score_gemma":0.0005597595,"threshold_uncertainty_score":0.010182917},"labels":[],"label_agreement":null},{"id":"W4390198822","doi":"10.1002/alz.077341","title":"Mild cognitive impairment in novel SPG4/SPAST mutation‐related sporadic late onset hereditary spastic paraplegia: case series","year":2023,"lang":"en","type":"article","venue":"Alzheimer s & Dementia","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":1,"is_retracted":false,"has_abstract":true,"route_ca_aff":false,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":true,"ca_institutions":"","funders":"","keywords":"Hereditary spastic paraplegia; Cognition; Medicine; Cognitive impairment; Montreal Cognitive Assessment; Genetics; Biology; Phenotype; Gene; Psychiatry","score_opus":0.046136715347427526,"score_gpt":0.27922973542775537,"score_spread":0.23309302008032784,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4390198822","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":[0.99602723,0.0011975383,0.0006277028,0.00017115803,0.000054801214,0.00007574795,0.00011352856,0.000042343785,0.0016898839],"genre_scores_gemma":[0.9986634,0.00037430038,0.00022925869,0.000118343596,0.00015435019,0.000016001592,0.00006845036,0.0000079541705,0.00036781098],"study_design_codex":"case_report","study_design_gemma":"case_report","domain_scores_codex":[0.999539,0.00004107176,0.000056535104,0.00015291697,0.0000698437,0.00014075673],"domain_scores_gemma":[0.999038,0.00019922503,0.00019339223,0.0001060432,0.00011160473,0.00035174415],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00032259303,0.0018609175,0.0010616027,0.0020512617,0.0016951801,0.0011435814,0.0010218142,0.002138251,0.001980761],"category_scores_gemma":[0.0017405081,0.0008794918,0.00097632484,0.0009985147,0.0014936484,0.0007110108,0.0011045324,0.0010606742,0.0006669479],"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":[0.000115135874,0.00017749846,0.039289735,0.00006809408,0.000054165004,0.9555585,0.0004489298,0.00007805029,0.001234407,0.000075612654,0.00033728965,0.002562686],"study_design_scores_gemma":[0.000024894429,0.00024857334,0.03880607,0.00001666124,0.000057963087,0.9593171,0.00018183501,0.0002473246,0.00051190756,0.00010631173,0.00045940885,0.000022009875],"about_ca_topic_score_codex":0.0031069075,"about_ca_topic_score_gemma":0.003280681,"teacher_disagreement_score":0.0031069075,"about_ca_system_score_codex":0.0008185016,"about_ca_system_score_gemma":0.00059580925,"threshold_uncertainty_score":0.0066262484},"labels":[],"label_agreement":null},{"id":"W4390261982","doi":"10.1016/j.jns.2023.121178","title":"Assessment of balance and falls in patients with hereditary spastic paraplegia","year":2023,"lang":"en","type":"article","venue":"Journal of the Neurological Sciences","topic":"Hereditary Neurological Disorders","field":"Neuroscience","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":"Université de Montréal","funders":"","keywords":"Hereditary spastic paraplegia; Paraplegia; Balance (ability); Physical medicine and rehabilitation; Spastic; Medicine; Physical therapy; Cerebral palsy; Psychiatry; Spinal cord; Biology; Genetics; Phenotype","score_opus":0.0288407643201119,"score_gpt":0.2768868551747187,"score_spread":0.24804609085460683,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4390261982","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":[0.99907696,0.00015317941,0.00005154851,0.000026198886,0.0000030943652,0.0000052610876,0.00006070894,0.000003826162,0.00061919633],"genre_scores_gemma":[0.99970263,0.000054168144,0.00006245642,0.000013625658,0.000003476095,0.0000039091283,0.00006243182,6.37148e-7,0.00009666595],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9997619,0.00005667177,0.000051575735,0.000031794774,0.000058288893,0.00003975465],"domain_scores_gemma":[0.9995285,0.00013807876,0.000121980105,0.000012996849,0.00008581661,0.000112571994],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0003063716,0.00045938167,0.00051739276,0.0011138248,0.00053856714,0.00045773198,0.00022590562,0.0005632967,0.00074874825],"category_scores_gemma":[0.0020862233,0.00014815698,0.00027947593,0.00058219733,0.00027040875,0.0003115477,0.00036476023,0.00029587361,0.00016455345],"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":[0.0003183356,0.00007642175,0.9941968,0.000015467731,0.000030343035,0.001309958,0.00013563369,0.000107489665,0.0006504757,0.000011584928,0.00007478983,0.0030727717],"study_design_scores_gemma":[0.0000109615185,0.00037326376,0.99464333,0.000009171513,0.0000282121,0.003827519,0.00028860715,0.000494897,0.00020148527,0.000044176984,0.000072258386,0.000006137138],"about_ca_topic_score_codex":0.00525954,"about_ca_topic_score_gemma":0.0073322677,"teacher_disagreement_score":0.00525954,"about_ca_system_score_codex":0.00033802856,"about_ca_system_score_gemma":0.0003017474,"threshold_uncertainty_score":0.010457873},"labels":[],"label_agreement":null},{"id":"W4390262326","doi":"10.1016/j.jns.2023.121179","title":"Vestibular evaluation in patients with hereditary spastic paraplegia","year":2023,"lang":"en","type":"article","venue":"Journal of the Neurological Sciences","topic":"Hereditary Neurological Disorders","field":"Neuroscience","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":"Université de Montréal","funders":"","keywords":"Hereditary spastic paraplegia; Paraplegia; Medicine; Physical medicine and rehabilitation; Spastic; Vestibular system; Physical therapy; Audiology; Spinal cord; Cerebral palsy; Biology; Psychiatry","score_opus":0.0548856929341394,"score_gpt":0.28384530121683127,"score_spread":0.22895960828269188,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4390262326","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":[0.99646014,0.00071373524,0.00009329494,0.00013784089,0.000015010531,0.000009949553,0.0000938373,0.000010081093,0.0024661701],"genre_scores_gemma":[0.9994375,0.00018479156,0.000051100622,0.000061331506,0.000015133301,0.0000027673063,0.000057032634,0.0000019906668,0.00018821858],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99972016,0.000043235992,0.000047419286,0.000044349785,0.00005318848,0.00009162614],"domain_scores_gemma":[0.9993248,0.00023693102,0.00012876176,0.000018928498,0.00009933243,0.00019129031],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00029648578,0.00060839765,0.0005403638,0.001770149,0.0008206153,0.00053463626,0.00033540383,0.00085437373,0.002425603],"category_scores_gemma":[0.0024280213,0.00019527583,0.0003023859,0.00077907165,0.00059587735,0.00047158395,0.000471959,0.00038918958,0.00028724104],"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":[0.00082117424,0.00013235322,0.91762906,0.000062807754,0.00004896261,0.07041194,0.00040858155,0.00018864685,0.003530215,0.000081229366,0.00039266382,0.0062923282],"study_design_scores_gemma":[0.00004307436,0.0005341035,0.8931714,0.00004757192,0.00008780075,0.10289271,0.0010771087,0.00059828564,0.0010056038,0.00017821779,0.00034168427,0.00002235681],"about_ca_topic_score_codex":0.006303516,"about_ca_topic_score_gemma":0.0057446742,"teacher_disagreement_score":0.006303516,"about_ca_system_score_codex":0.0005457433,"about_ca_system_score_gemma":0.00057123567,"threshold_uncertainty_score":0.012533665},"labels":[],"label_agreement":null},{"id":"W4390395475","doi":"10.1002/mus.28032","title":"Home‐based multi‐sensory and proximal strengthening program to improve balance in<scp>Charcot–Marie–Tooth disease Type 1A: A</scp>proof of concept study","year":2023,"lang":"en","type":"article","venue":"Muscle & Nerve","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":10,"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 College London Hospitals Biomedical Research Centre; Medical Research Council; Medical Research Council Canada; University College London; National Center for Advancing Translational Sciences; Kingston University; National Institute for Health and Care Research; Muscular Dystrophy Association; Rare Diseases Clinical Research Network; Charcot-Marie-Tooth Association","keywords":"Balance (ability); Proprioception; Physical medicine and rehabilitation; Tooth disease; Physical therapy; Medicine; Rehabilitation; Psychological intervention; Disease; Psychology; Gerontology; Pathology; Nursing","score_opus":0.04675634864722064,"score_gpt":0.29562775382865913,"score_spread":0.2488714051814385,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4390395475","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":[0.9884862,0.0014676842,0.0017931144,0.00030519083,0.0001406418,0.0066894456,0.0004698847,0.00006430765,0.00058336946],"genre_scores_gemma":[0.962347,0.0039151968,0.017168667,0.0006286868,0.00023771361,0.013317414,0.0007347129,0.000027097423,0.0016235143],"study_design_codex":"nonrandomized_trial","study_design_gemma":"nonrandomized_trial","domain_scores_codex":[0.9992994,0.00030508064,0.000043861506,0.000100130346,0.00014413876,0.000107439446],"domain_scores_gemma":[0.99937147,0.0001698186,0.00012799146,0.000037740327,0.00010470444,0.0001883178],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0023768628,0.0010696338,0.0012613301,0.00060009013,0.00046773962,0.00062809733,0.0013985179,0.0015100554,0.0044854945],"category_scores_gemma":[0.00088261644,0.00032570245,0.00168395,0.0002996746,0.0007536537,0.0006346076,0.00053698226,0.0012700212,0.0004039449],"study_design_candidate":"nonrandomized_trial","study_design_consensus":"nonrandomized_trial","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.18327044,0.49426132,0.0034462933,0.012731298,0.002418311,0.0007990929,0.00053944165,0.0012719369,0.15370226,0.00034896334,0.002727613,0.14448306],"study_design_scores_gemma":[0.12168217,0.8538281,0.009161412,0.00034425413,0.0008953118,0.0002894714,0.00014921017,0.0008029948,0.010731259,0.00008594542,0.0019997896,0.000030236071],"about_ca_topic_score_codex":0.0009047424,"about_ca_topic_score_gemma":0.0012300793,"teacher_disagreement_score":0.0044854945,"about_ca_system_score_codex":0.00037960924,"about_ca_system_score_gemma":0.0015498461,"threshold_uncertainty_score":0.015005469},"labels":[],"label_agreement":null},{"id":"W4390574251","doi":"10.1038/s41598-023-51137-6","title":"Transcriptome analysis in a humanized mouse model of familial dysautonomia reveals tissue-specific gene expression disruption in the peripheral nervous system","year":2024,"lang":"en","type":"article","venue":"Scientific Reports","topic":"Hereditary Neurological Disorders","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 Institutes of Health; National Institute of Neurological Disorders and Stroke; York University; PTC Therapeutics","keywords":"Transcriptome; Humanized mouse; Dysautonomia; Familial dysautonomia; Peripheral; Gene expression; Peripheral nervous system; Biology; Neuroscience; Gene; Nervous system; Medicine; Central nervous system; Pathology; Immunology; Genetics; Immune system; Internal medicine; Disease","score_opus":0.04207333412767699,"score_gpt":0.27623146766314394,"score_spread":0.23415813353546694,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4390574251","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":[0.98937374,0.0009246003,0.0051544034,0.00007730317,0.000037220267,0.00003847277,0.0036736364,0.0001421446,0.00057848974],"genre_scores_gemma":[0.9803934,0.0011607658,0.007640383,0.00014539158,0.0000104865585,0.00015975544,0.0053674085,0.00007786557,0.0050445604],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9997924,0.000010658654,0.000014655888,0.00009161651,0.000055843466,0.000034800178],"domain_scores_gemma":[0.9999105,0.000009552914,0.000035172194,0.000009375107,0.000011374157,0.00002410018],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.000104725485,0.0003844467,0.00027168693,0.0006037076,0.00019219524,0.00027358026,0.00015169577,0.0003007026,0.0010023525],"category_scores_gemma":[0.00007166236,0.00018221696,0.00039667086,0.00029911942,0.0002718893,0.00013001433,0.00017807729,0.00054842955,0.00029494532],"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":[0.00007158231,0.000009585703,0.00023851331,0.000016782908,0.000004780529,0.00004435014,0.000009272928,0.000026298127,0.99922216,0.000018048237,0.000019081874,0.0003195437],"study_design_scores_gemma":[0.000036709247,0.0005413938,0.05821348,0.000024981231,0.00011489514,0.0013331039,0.00019077328,0.0023006524,0.9334775,0.00014026766,0.0036103802,0.000015849626],"about_ca_topic_score_codex":0.0006772668,"about_ca_topic_score_gemma":0.0012353507,"teacher_disagreement_score":0.0010023525,"about_ca_system_score_codex":0.00025117648,"about_ca_system_score_gemma":0.00016663308,"threshold_uncertainty_score":0.0033531785},"labels":[],"label_agreement":null},{"id":"W4390691335","doi":"10.1101/2024.01.09.24301064","title":"Towards patient-relevant, trial-ready digital motor outcomes for SPG7: a cross-sectional prospective multi-center study (PROSPAX)","year":2024,"lang":"en","type":"preprint","venue":"medRxiv","topic":"Hereditary Neurological Disorders","field":"Neuroscience","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":"Centre Intégré Universitaire de Santé et de Services Sociaux du Saguenay–Lac-Saint-Jean; Université de Sherbrooke","funders":"Koç Üniversitesi Translasyonel Tıp Araştırma Merkezi; International Max Planck Research School for Advanced Methods in Process and Systems Engineering; Servier; Radboud Universitair Medisch Centrum; Ministero della Salute; Else Kröner-Fresenius-Stiftung; Bundesministerium für Bildung und Forschung; Hersenstichting; Eberhard Karls Universität Tübingen; Türkiye Bilimsel ve Teknolojik Araştırma Kurumu; Radboud Universiteit; Ionis Pharmaceuticals; ZonMw; International Max Planck Research School for Environmental, Cellular and Molecular Microbiology; Deutsche Forschungsgemeinschaft; Eli Lilly and Company","keywords":"Physical medicine and rehabilitation; Gait; Medicine; STRIDE; Physical therapy","score_opus":0.08788925221310602,"score_gpt":0.35696613365359203,"score_spread":0.269076881440486,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4390691335","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":[0.99224174,0.001446544,0.001554856,0.00016299497,0.00004746637,0.0020131492,0.0018647829,0.00002075397,0.0006477862],"genre_scores_gemma":[0.99102485,0.0002374519,0.0025634023,0.00030845503,0.00006833711,0.0030214242,0.0025459824,0.000012664469,0.00021747086],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9863304,0.009793385,0.0014849466,0.0013657034,0.0006633624,0.00036222357],"domain_scores_gemma":[0.9820724,0.0055493014,0.005599464,0.0024986148,0.002850078,0.0014301792],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.02097419,0.00083694403,0.0011493148,0.0008352144,0.0011071396,0.0012769628,0.0006873764,0.0013582497,0.0025996915],"category_scores_gemma":[0.015404584,0.00050284044,0.0015409449,0.0012098385,0.0009347256,0.0013618201,0.001537732,0.0007903166,0.0008851835],"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":[0.037301995,0.0023065547,0.9374547,0.0014826554,0.0033425477,0.00016312306,0.00062725093,0.0003058674,0.0019827024,0.00029486237,0.001443772,0.013293994],"study_design_scores_gemma":[0.009487755,0.034370616,0.9477013,0.00034266256,0.002351046,0.00040794243,0.0005059209,0.0005366082,0.0011184836,0.0003473754,0.002779706,0.000050614817],"about_ca_topic_score_codex":0.0007211157,"about_ca_topic_score_gemma":0.001311461,"teacher_disagreement_score":0.02097419,"about_ca_system_score_codex":0.0004677465,"about_ca_system_score_gemma":0.0012728804,"threshold_uncertainty_score":0.11092347},"labels":[],"label_agreement":null},{"id":"W4391143049","doi":"10.1007/s00415-023-12159-2","title":"Neuropathy in ARSACS is demyelinating but without typical nerve enlargement in nerve ultrasound","year":2024,"lang":"en","type":"article","venue":"Journal of Neurology","topic":"Hereditary Neurological Disorders","field":"Neuroscience","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":"Universitätsklinikum Tübingen; Deutsche Forschungsgemeinschaft","keywords":"Medicine; Spasticity; Peripheral neuropathy; Median nerve; Neuroradiology; Ultrasound; Ulnar nerve; Nerve biopsy; Nerve conduction study; Neurology; Pathology; Nerve conduction; Anatomy; Internal medicine; Radiology; Anesthesia; Endocrinology","score_opus":0.03462668480418374,"score_gpt":0.29691720164779833,"score_spread":0.2622905168436146,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4391143049","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":[0.99840575,0.00032664294,0.0001862757,0.000026571526,0.0000067105216,0.00001240759,0.00006693715,0.000009962032,0.00095876004],"genre_scores_gemma":[0.9992169,0.00016956271,0.0002504627,0.00003142391,0.000016543407,0.0000064518863,0.00012356565,0.00000313421,0.0001819307],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99967885,0.000052655152,0.000059933172,0.00007337909,0.00007327391,0.00006189855],"domain_scores_gemma":[0.9986071,0.0003836503,0.0005824692,0.00006893939,0.00017135344,0.0001865766],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0005608778,0.0008307256,0.00047893505,0.0012870266,0.00052286184,0.0005641623,0.00040032205,0.00055670674,0.002965188],"category_scores_gemma":[0.0015802282,0.0001689792,0.00021783044,0.0009624587,0.0006713533,0.00037539456,0.0004225101,0.00028051835,0.0003946358],"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":[0.00040496088,0.00009642024,0.9520228,0.00014472239,0.00003866733,0.029622728,0.00035632428,0.0001747041,0.010866847,0.00014972333,0.00023358692,0.0058884327],"study_design_scores_gemma":[0.000027410433,0.00075916195,0.81339395,0.0000892411,0.00007026619,0.18191434,0.00051547936,0.000338137,0.00173772,0.00017974203,0.0009575218,0.000016981052],"about_ca_topic_score_codex":0.0019278921,"about_ca_topic_score_gemma":0.0027052485,"teacher_disagreement_score":0.002965188,"about_ca_system_score_codex":0.0002395619,"about_ca_system_score_gemma":0.00045701963,"threshold_uncertainty_score":0.009919524},"labels":[],"label_agreement":null},{"id":"W4391286308","doi":"10.14740/jmc4174","title":"Hip Dysplasia in a Patient in Late Adolescence With Charcot-Marie-Tooth and Multiple Acyl-CoA Dehydrogenase Deficiency","year":2024,"lang":"en","type":"article","venue":"Journal of Medical Cases","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":0,"is_retracted":false,"has_abstract":true,"route_ca_aff":false,"route_ca_fund":false,"route_ca_venue":true,"route_about_ca":false,"ca_institutions":"","funders":"","keywords":"Medicine; Hip dysplasia; Presentation (obstetrics); Dysplasia; Tooth disease; Disease; Pediatrics; Case presentation; Surgery; Internal medicine","score_opus":0.027600631772104662,"score_gpt":0.2675813994859391,"score_spread":0.23998076771383445,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4391286308","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":[0.98135364,0.0038670334,0.0021323664,0.0032368596,0.0003107065,0.00012070393,0.00020088229,0.00009240598,0.008685351],"genre_scores_gemma":[0.99561656,0.0012397188,0.0010693488,0.00064166647,0.0003264793,0.000016599177,0.000050903607,0.00001625474,0.0010224032],"study_design_codex":"case_report","study_design_gemma":"case_report","domain_scores_codex":[0.99956566,0.00005373719,0.00004775821,0.000103635095,0.00009306327,0.00013609526],"domain_scores_gemma":[0.99915004,0.00020126601,0.00020618613,0.000027619248,0.00006107756,0.00035378913],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00029979748,0.0010897284,0.0009229915,0.0023862703,0.0021713204,0.00096529134,0.00063035754,0.002803348,0.0016630739],"category_scores_gemma":[0.0023083296,0.0007189702,0.00060643716,0.0011011175,0.00091178936,0.001087401,0.0014335336,0.001989792,0.00038906344],"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":[0.000009472123,0.00002268786,0.008545986,0.000014230817,0.0000040204877,0.9899413,0.00019287237,0.000028963583,0.00028270326,0.00009438961,0.00014101858,0.00072234427],"study_design_scores_gemma":[0.000001984863,0.000019539799,0.003921387,0.0000088183115,0.0000039771817,0.99558616,0.00009599636,0.000042445125,0.00007138172,0.00005689723,0.00018712386,0.0000043190767],"about_ca_topic_score_codex":0.0035436857,"about_ca_topic_score_gemma":0.0064208885,"teacher_disagreement_score":0.0035436857,"about_ca_system_score_codex":0.0008694813,"about_ca_system_score_gemma":0.0009550037,"threshold_uncertainty_score":0.0070461035},"labels":[],"label_agreement":null},{"id":"W4392464997","doi":"10.1002/cne.25596","title":"Pathologic classification of a late‐onset peripheral neuropathy in a spontaneous Labrador retriever dog model","year":2024,"lang":"en","type":"article","venue":"The Journal of Comparative Neurology","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":2,"is_retracted":false,"has_abstract":true,"route_ca_aff":false,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":true,"ca_institutions":"","funders":"National Institutes of Health; National Cancer Institute; American College of Veterinary Surgeons Foundation; U.S. National Library of Medicine; University of Wisconsin Carbone Cancer Center","keywords":"Paresis; Medicine; Compound muscle action potential; Peripheral; Electromyography; Nerve conduction velocity; Peripheral neuropathy; Anatomy; Sciatic nerve; Paralysis; Ulnar nerve; Peripheral nervous system; Electrophysiology; Internal medicine; Surgery; Central nervous system; Elbow; Physical medicine and rehabilitation","score_opus":0.07198171556549056,"score_gpt":0.31720467365637667,"score_spread":0.24522295809088612,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4392464997","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":[0.9956462,0.00061116973,0.001911767,0.000027853672,0.00002027954,0.00015880424,0.00025912252,0.000049000515,0.0013157445],"genre_scores_gemma":[0.99316484,0.00054612366,0.0026023234,0.00004760795,0.000013494361,0.00018583871,0.0011942324,0.000014073019,0.0022314931],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9997516,0.000042607757,0.000030320483,0.00008022877,0.00005106143,0.00004430214],"domain_scores_gemma":[0.9997392,0.000028758233,0.00008387449,0.000037215923,0.000053314223,0.000057554193],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0006027406,0.0004452611,0.0003474571,0.00088534586,0.00023248237,0.0003628437,0.00027600443,0.000542672,0.0010936164],"category_scores_gemma":[0.00030835954,0.0001713683,0.00028351875,0.00018001204,0.00037427613,0.00038978015,0.00022992089,0.00029705281,0.00028122694],"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":[0.0015237608,0.000740937,0.024366371,0.00018816364,0.000070554175,0.002095372,0.00017318338,0.00037426164,0.96366817,0.0003890518,0.00027457217,0.0061356253],"study_design_scores_gemma":[0.00048768814,0.026895206,0.46085125,0.00018839944,0.00060218544,0.035511553,0.0009241854,0.010651075,0.45249876,0.00054358767,0.010757644,0.00008846633],"about_ca_topic_score_codex":0.0009068241,"about_ca_topic_score_gemma":0.0022026447,"teacher_disagreement_score":0.0010936164,"about_ca_system_score_codex":0.0004391726,"about_ca_system_score_gemma":0.00021879023,"threshold_uncertainty_score":0.003658533},"labels":[],"label_agreement":null},{"id":"W4393996955","doi":"10.3233/jnd-230230","title":"Novel Genetic and Biochemical Insights into the Spectrum of <i>NEFL</i> -Associated Phenotypes","year":2024,"lang":"en","type":"article","venue":"Journal of Neuromuscular Diseases","topic":"Hereditary Neurological Disorders","field":"Neuroscience","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":"University of Ottawa; Ottawa Hospital; Children's Hospital of Eastern Ontario","funders":"","keywords":"Phenotype; Genetics; Myopathy; Medicine; Biology; Bioinformatics; Gene","score_opus":0.014253282374511754,"score_gpt":0.23472169691027472,"score_spread":0.22046841453576296,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4393996955","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":[0.982298,0.0050330134,0.006792842,0.0003677895,0.000035183726,0.00004478955,0.0008548118,0.0001709776,0.004402694],"genre_scores_gemma":[0.9887074,0.0023102106,0.0072065387,0.00019882336,0.00006946811,0.000022317854,0.00083402015,0.00002980421,0.0006214972],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9998665,0.000019635037,0.000020905674,0.000045099107,0.000026325624,0.000021522732],"domain_scores_gemma":[0.9997528,0.0000663533,0.00010367575,0.00001525068,0.000030696043,0.00003116068],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00020371619,0.0009703189,0.0002762148,0.0013894406,0.00020811096,0.0004072892,0.0003924239,0.00072343426,0.0017957892],"category_scores_gemma":[0.000446034,0.00016488455,0.0004712076,0.0006203206,0.00046522063,0.0003779354,0.00040147183,0.0003693341,0.0004520719],"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":[0.0008413451,0.00023734263,0.1556159,0.00081259734,0.00021162844,0.21905135,0.00075396476,0.0012109731,0.57428056,0.0018820532,0.0013776515,0.043724615],"study_design_scores_gemma":[0.00005125131,0.00063711096,0.25534454,0.00025842607,0.00033205954,0.6561098,0.0006704322,0.0028784033,0.06517967,0.0028487158,0.015628131,0.0000614102],"about_ca_topic_score_codex":0.00030534662,"about_ca_topic_score_gemma":0.00034023987,"teacher_disagreement_score":0.0017957892,"about_ca_system_score_codex":0.00016051138,"about_ca_system_score_gemma":0.00014152021,"threshold_uncertainty_score":0.006007552},"labels":[],"label_agreement":null},{"id":"W4394599333","doi":"10.1212/wnl.0000000000206081","title":"A Case of Parakinesia Brachialis Oscitans and Excessive Yawning from Tumefactive Demyelination (P5-4.011)","year":2024,"lang":"en","type":"article","venue":"Neurology","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":false,"ca_institutions":"University of British Columbia","funders":"","keywords":"Brachialis; Medicine; Anatomy","score_opus":0.030391123736691263,"score_gpt":0.2835020074047119,"score_spread":0.2531108836680206,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4394599333","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":[0.9904822,0.0019555509,0.00095191697,0.0005545696,0.00015727406,0.00004291739,0.00007681302,0.00006551045,0.0057131774],"genre_scores_gemma":[0.99764615,0.00040120445,0.0004790192,0.00020200798,0.00023300388,0.00001385363,0.0000491788,0.000009110107,0.0009665036],"study_design_codex":"case_report","study_design_gemma":"case_report","domain_scores_codex":[0.99961084,0.000043109812,0.000050776398,0.00009323084,0.000042693024,0.00015938535],"domain_scores_gemma":[0.99894863,0.00030011023,0.00026414968,0.00012712389,0.000051729065,0.0003083867],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00031010422,0.0014653871,0.0005942712,0.001602484,0.0019783098,0.0008779801,0.0007647615,0.002627702,0.0022320452],"category_scores_gemma":[0.002188494,0.00082661706,0.0005813611,0.001223278,0.0013935448,0.0009304424,0.001623708,0.0015858609,0.00075140345],"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":[0.00005627872,0.00002624482,0.005809943,0.000029259816,0.000008352395,0.9912934,0.00020301643,0.000038696882,0.0013816102,0.00017573764,0.000111763504,0.00086567696],"study_design_scores_gemma":[0.000025281915,0.00008747198,0.0061398214,0.000006167027,0.0000151472395,0.99227893,0.00009096582,0.000106050145,0.00058666203,0.00017363706,0.00048196057,0.000007958426],"about_ca_topic_score_codex":0.0019781382,"about_ca_topic_score_gemma":0.0016698375,"teacher_disagreement_score":0.002627702,"about_ca_system_score_codex":0.0006609805,"about_ca_system_score_gemma":0.00048550928,"threshold_uncertainty_score":0.0074669123},"labels":[],"label_agreement":null},{"id":"W4394763476","doi":"10.1038/s41598-024-58278-2","title":"SNORA69 is up-regulated in the lateral habenula of individuals with major depressive disorder","year":2024,"lang":"en","type":"article","venue":"Scientific Reports","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":6,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"McGill University; Douglas Mental Health University Institute","funders":"Fonds de Recherche du Québec - Santé; Canadian Institutes of Health Research","keywords":"Habenula; Major depressive disorder; Computer science; Medicine; Neuroscience; Psychiatry; Biology; Psychology; Central nervous system; Mood","score_opus":0.019501339318782035,"score_gpt":0.2619707656731053,"score_spread":0.24246942635432325,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4394763476","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":[0.99868435,0.00031760885,0.00015222335,0.000033634962,0.000005090766,0.000004311981,0.0003534526,0.000011741564,0.00043749987],"genre_scores_gemma":[0.99850625,0.00017807493,0.0002993535,0.00005226459,0.0000036547315,0.000008864257,0.00029876083,0.000005638646,0.0006470041],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9999473,0.0000063821717,0.0000038433245,0.000019121544,0.00001347346,0.000009907523],"domain_scores_gemma":[0.9999236,0.0000058801274,0.00003922955,0.0000045934885,0.000010549654,0.00001611483],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00005685741,0.00011493995,0.00015417421,0.0003099331,0.00019358216,0.00016498724,0.000062652514,0.00012849933,0.0015550576],"category_scores_gemma":[0.00015891812,0.00008651878,0.00009661587,0.00013307288,0.00014841784,0.000060226797,0.00017618635,0.00014401852,0.00017644744],"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":[0.0017655595,0.000067551,0.3033721,0.000118036645,0.00018779743,0.0013099464,0.0005009694,0.00010296585,0.6711386,0.00016523905,0.0007137827,0.020557482],"study_design_scores_gemma":[0.000007631433,0.00007671278,0.9924505,0.0000095099795,0.00002796354,0.00062227494,0.00013920556,0.00009486849,0.0060078735,0.000055242075,0.0005043319,0.0000038870007],"about_ca_topic_score_codex":0.0019188155,"about_ca_topic_score_gemma":0.006033273,"teacher_disagreement_score":0.0019188155,"about_ca_system_score_codex":0.00015361395,"about_ca_system_score_gemma":0.00009550185,"threshold_uncertainty_score":0.005202174},"labels":[],"label_agreement":null},{"id":"W4394987472","doi":"10.1101/2024.04.18.590157","title":"Characterization of a novel zebrafish model of <i>MTMR5</i> -associated CMT4B3","year":2024,"lang":"en","type":"preprint","venue":"bioRxiv (Cold Spring Harbor Laboratory)","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":0,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Canada Research Chairs; Hospital for Sick Children; University of Toronto; University of New Brunswick","funders":"Natural Sciences and Engineering Research Council of Canada; Hospital for Sick Children","keywords":"Zebrafish; Phenocopy; Biology; Disease; Pathology; Mutant; Neuroscience; Genetics; Medicine; Gene","score_opus":0.03316479202023811,"score_gpt":0.22608434000586686,"score_spread":0.19291954798562874,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4394987472","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":[0.9060924,0.0018049568,0.06917281,0.0020200403,0.0004485086,0.0012302909,0.006470509,0.0017716071,0.010989003],"genre_scores_gemma":[0.91716284,0.0017336413,0.047906533,0.00056007603,0.00003719991,0.0014443527,0.0043200566,0.0006419418,0.026193354],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9996126,0.000027270476,0.0000382053,0.00008676439,0.00016980692,0.000065278],"domain_scores_gemma":[0.9996412,0.000031352498,0.00010996985,0.000025376807,0.00006679601,0.00012523249],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0005166331,0.0007186613,0.0005026986,0.00092331786,0.0007730316,0.0005046057,0.00084914855,0.0012941178,0.0035070046],"category_scores_gemma":[0.00034655328,0.00039449832,0.00079475954,0.00017917909,0.0006919222,0.00048190344,0.00068212504,0.0015864363,0.0012754162],"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":[0.00006296402,0.00003144077,0.00020345046,0.000053065636,0.000008856181,0.00047301373,0.00004670622,0.000114141156,0.99693847,0.0006550928,0.00033408747,0.0010786646],"study_design_scores_gemma":[0.00020079127,0.001373445,0.00885444,0.00012350234,0.00016180488,0.005868026,0.00026011223,0.005510372,0.9503634,0.00062376435,0.026564837,0.00009546363],"about_ca_topic_score_codex":0.009637693,"about_ca_topic_score_gemma":0.013592759,"teacher_disagreement_score":0.009637693,"about_ca_system_score_codex":0.0013574498,"about_ca_system_score_gemma":0.0010352194,"threshold_uncertainty_score":0.019163191},"labels":[],"label_agreement":null},{"id":"W4395083859","doi":"10.1097/mop.0000000000001354","title":"Emerging therapies for childhood-onset movement disorders","year":2024,"lang":"en","type":"review","venue":"Current Opinion in Pediatrics","topic":"Hereditary Neurological Disorders","field":"Neuroscience","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":"Centre for Movement Disorders; Hospital for Sick Children","funders":"National Institute of Neurological Disorders and Stroke; National Institutes of Health; Spastic Paraplegia Foundation; Eunice Kennedy Shriver National Institute of Child Health and Human Development; International Parkinson and Movement Disorder Society","keywords":"Medicine; Movement disorders; Deep brain stimulation; Ataxia; Disease; Mechanism (biology); Essential tremor; Tourette syndrome; Bioinformatics; Neuroscience; Psychiatry; Parkinson's disease; Psychology; Pathology","score_opus":0.11235628689239925,"score_gpt":0.4020684434910959,"score_spread":0.28971215659869665,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4395083859","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":[0.00008554321,0.9977543,0.00014524326,0.0003458591,0.00033286773,0.0000060554453,0.000018380133,0.000011527392,0.0013002467],"genre_scores_gemma":[0.00048168347,0.998071,0.0002391899,0.00029586052,0.00024894546,0.000008057807,0.0000298362,0.0000025440463,0.00062289607],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.9998667,0.000024003502,0.000021143962,0.00002195636,0.00005076436,0.00001537354],"domain_scores_gemma":[0.99979264,0.00009934036,0.000032895285,0.000005764788,0.00005057722,0.000018892099],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0004010654,0.00088370696,0.00091722165,0.001532714,0.00022446194,0.0007097127,0.0005928196,0.0008366386,0.0049614166],"category_scores_gemma":[0.0005726205,0.00015317691,0.00041965774,0.0010843462,0.00033864853,0.00091323437,0.0006446737,0.0016605541,0.0025047495],"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":[0.000055312885,0.00004918898,0.000112767164,0.018580548,0.0000769615,0.0002799227,0.00005784647,0.00031329473,0.0016249069,0.005117238,0.04849069,0.92524135],"study_design_scores_gemma":[0.0000144931655,0.00006021905,0.00044735958,0.005318853,0.00007503307,0.0014146196,0.000047245383,0.00006845809,0.0003438344,0.0017046662,0.9904953,0.000009895334],"about_ca_topic_score_codex":0.00074015255,"about_ca_topic_score_gemma":0.0016482382,"teacher_disagreement_score":0.0049614166,"about_ca_system_score_codex":0.00058782246,"about_ca_system_score_gemma":0.00096882804,"threshold_uncertainty_score":0.016597629},"labels":[],"label_agreement":null},{"id":"W4396780077","doi":"10.1016/j.jeph.2024.202502","title":"P62 - Modélisation médico-économique de la toxine botulique dans la prise en charge des dysménorrhées sévères","year":2024,"lang":"fr","type":"article","venue":"Journal of Epidemiology and Population Health","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":false,"ca_institutions":"Université Laval; Centre hospitalier de l'Université Laval","funders":"","keywords":"Physics","score_opus":0.08094466765107053,"score_gpt":0.38080792259277735,"score_spread":0.29986325494170685,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4396780077","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":[0.6162263,0.00506832,0.33160314,0.0056071985,0.0006002648,0.00041850758,0.003712457,0.0012681716,0.035495713],"genre_scores_gemma":[0.9613484,0.0011682711,0.019900821,0.00023151342,0.0000638251,0.00025718132,0.0008452453,0.000051452647,0.016133305],"study_design_codex":"simulation_or_modeling","study_design_gemma":"simulation_or_modeling","domain_scores_codex":[0.99950135,0.00022995663,0.000018065784,0.00008668823,0.000055533772,0.00010834831],"domain_scores_gemma":[0.99723804,0.0021524332,0.00018181872,0.000044835575,0.00028954833,0.00009334223],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0017432385,0.00088089117,0.0011456017,0.0006191564,0.00053000485,0.0016766647,0.0011345478,0.0018788261,0.0077913958],"category_scores_gemma":[0.0047062924,0.0005702714,0.0013954252,0.00057440007,0.0005356909,0.00069976045,0.00080493226,0.0017059653,0.0005521291],"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":[0.000093966104,0.000037184753,0.0013807698,0.000043415166,0.000031468608,0.00003404298,0.000014014313,0.99199367,0.00013264873,0.0020153532,0.00037813903,0.0038452395],"study_design_scores_gemma":[0.000015865242,0.000042065803,0.00034201864,0.000010622114,0.00001668477,0.0000067205283,0.0000108637905,0.9982577,0.000063716885,0.0009132643,0.00031644545,0.000004168921],"about_ca_topic_score_codex":0.07119281,"about_ca_topic_score_gemma":0.032183,"teacher_disagreement_score":0.07119281,"about_ca_system_score_codex":0.0017000329,"about_ca_system_score_gemma":0.0033909208,"threshold_uncertainty_score":0.1415568},"labels":[],"label_agreement":null},{"id":"W4396879455","doi":"10.21037/jlpm-23-71","title":"Unraveling the diagnostic enigma: laboratory diagnosis of sphingolipid activator protein deficiencies","year":2024,"lang":"en","type":"article","venue":"Journal of Laboratory and Precision Medicine","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":1,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Hospital for Sick Children; University of Toronto","funders":"","keywords":"Sphingolipid; Activator (genetics); Biology; Computational biology; Cell biology; Biochemistry; Receptor","score_opus":0.028379276786982585,"score_gpt":0.282687942436983,"score_spread":0.2543086656500004,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4396879455","genre_codex":"review","genre_gemma":"methods","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"methods","genre_consensus":null,"domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.10652032,0.47821355,0.0707367,0.31240797,0.009038013,0.00020778153,0.00088672346,0.0015609049,0.020428015],"genre_scores_gemma":[0.6534931,0.20870951,0.060798135,0.050892234,0.021755084,0.0001535554,0.0011502657,0.00027101414,0.0027770645],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.9969733,0.0010162377,0.0004861663,0.000391551,0.00084876403,0.00028385333],"domain_scores_gemma":[0.9907862,0.0042288536,0.0006888465,0.0005021473,0.0030292342,0.00076482206],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.005479397,0.0014592168,0.0016472241,0.0048285713,0.0010247354,0.00245363,0.002629602,0.0032180485,0.0018609539],"category_scores_gemma":[0.01840533,0.0006537682,0.00069733436,0.0015000628,0.0026052648,0.005434041,0.0018457087,0.009219331,0.0010984819],"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":[0.0006661151,0.0003720509,0.15730143,0.002483292,0.00045408384,0.116108045,0.001688013,0.0025882013,0.01613379,0.025787896,0.17097968,0.5054373],"study_design_scores_gemma":[0.00019548224,0.000472679,0.033993423,0.00917276,0.0008423991,0.61235666,0.005521823,0.01768652,0.007983209,0.09897191,0.21246973,0.0003333768],"about_ca_topic_score_codex":0.002677925,"about_ca_topic_score_gemma":0.0016226819,"teacher_disagreement_score":0.005479397,"about_ca_system_score_codex":0.0016948001,"about_ca_system_score_gemma":0.0014099509,"threshold_uncertainty_score":0.028978169},"labels":[],"label_agreement":null},{"id":"W4396890767","doi":"10.1101/2024.05.10.24306768","title":"Biallelic variants in <i>ARHGAP19</i> cause a motor-predominant neuropathy with asymmetry and conduction slowing","year":2024,"lang":"en","type":"preprint","venue":"medRxiv","topic":"Hereditary Neurological Disorders","field":"Neuroscience","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 Health Centre; McGill University","funders":"Medical Research Council","keywords":"Zebrafish; Biology; RHOA; Loss function; Gene knockdown; Phenotype; Genetics; Drosophila melanogaster; Neuroscience; GTPase; Gene; Signal transduction","score_opus":0.04235188471353906,"score_gpt":0.2669595185591966,"score_spread":0.22460763384565752,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4396890767","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":[0.9883652,0.0007383803,0.0035235458,0.00030216057,0.00008208599,0.00005432429,0.0016493154,0.00024833233,0.0050366586],"genre_scores_gemma":[0.99487996,0.0003160208,0.0015861749,0.00013712904,0.00005329927,0.000015365293,0.0007714863,0.000046574674,0.0021940493],"study_design_codex":"bench_or_experimental","study_design_gemma":"case_report","domain_scores_codex":[0.9998598,0.000016677077,0.00001425688,0.000052977408,0.00003414019,0.000022071972],"domain_scores_gemma":[0.9999106,0.000015529886,0.000034199868,0.000007802002,0.000007138289,0.000024720197],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00011932439,0.00088080176,0.00024499826,0.0004351968,0.0003030615,0.00022854829,0.00021199591,0.0004678143,0.0036657439],"category_scores_gemma":[0.00014983655,0.00012370937,0.00027326614,0.00028344902,0.0002991622,0.00009977397,0.00040770657,0.00039195883,0.0007251191],"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":[0.0007064841,0.00013766282,0.03411242,0.00015527256,0.00019264329,0.049443714,0.00027619995,0.00033613484,0.89271396,0.0011826085,0.0035563759,0.017186448],"study_design_scores_gemma":[0.00019654029,0.00068163354,0.43752646,0.00011592804,0.00037775323,0.2371028,0.00039691062,0.0027580564,0.29315078,0.0014743897,0.02616564,0.00005311253],"about_ca_topic_score_codex":0.0006893001,"about_ca_topic_score_gemma":0.0010741947,"teacher_disagreement_score":0.0036657439,"about_ca_system_score_codex":0.0001886231,"about_ca_system_score_gemma":0.000121079174,"threshold_uncertainty_score":0.012263119},"labels":[],"label_agreement":null},{"id":"W4398171678","doi":"10.20944/preprints202405.1279.v1","title":"Compound Heterozygous Mutations of SACS in a Korean Cohort Study of Charcot-Marie-Tooth Disease Concurrent Cerebellar Ataxia and Spasticity","year":2024,"lang":"en","type":"preprint","venue":"Preprints.org","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":1,"is_retracted":false,"has_abstract":true,"route_ca_aff":false,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":true,"ca_institutions":"","funders":"","keywords":"Tooth disease; Spasticity; Ataxia; Cerebellar ataxia; Cohort; Medicine; Mutation; Genetics; Disease; Biology; Physical medicine and rehabilitation; Internal medicine; Gene; Psychiatry","score_opus":0.12239997854731564,"score_gpt":0.34740832431335283,"score_spread":0.22500834576603718,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4398171678","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":[0.99954236,0.00005122919,0.00006021354,0.000016827169,0.0000052355485,0.000012532064,0.00018218759,0.0000022620932,0.00012722395],"genre_scores_gemma":[0.9992544,0.00009767965,0.000121946076,0.000033534277,0.0000074041204,0.0000111996205,0.00030505817,0.0000052470846,0.00016346692],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99960035,0.000044376877,0.000058324847,0.00018039106,0.00005858708,0.000058002403],"domain_scores_gemma":[0.99941194,0.000041398063,0.00013499877,0.00007036073,0.00010148675,0.00023978665],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00043813788,0.0007770409,0.0005394195,0.0010112142,0.0010277198,0.0006631798,0.00039614105,0.00048307047,0.0018935971],"category_scores_gemma":[0.0010211315,0.0007359283,0.00056816067,0.0010213354,0.0003364051,0.0004541525,0.0007385084,0.00041693446,0.0003987443],"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":[0.00026937586,0.00010680284,0.98835677,0.00001895671,0.00014610696,0.0044340524,0.0005592814,0.00005747943,0.0040221997,0.00006852025,0.00034208407,0.0016183167],"study_design_scores_gemma":[0.000060388582,0.00031482312,0.982894,0.000018804496,0.00019732659,0.013757638,0.00114944,0.0003059984,0.00041824827,0.000068479305,0.0007870773,0.000027845337],"about_ca_topic_score_codex":0.011552877,"about_ca_topic_score_gemma":0.010979946,"teacher_disagreement_score":0.011552877,"about_ca_system_score_codex":0.00036173107,"about_ca_system_score_gemma":0.0006445736,"threshold_uncertainty_score":0.022971272},"labels":[],"label_agreement":null},{"id":"W4398255835","doi":"10.1017/cjn.2024.168","title":"P.062 Normal NCS in 42-year-old man with PMP22 duplication","year":2024,"lang":"en","type":"article","venue":"Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":0,"is_retracted":false,"has_abstract":true,"route_ca_aff":false,"route_ca_fund":false,"route_ca_venue":true,"route_about_ca":false,"ca_institutions":"","funders":"","keywords":"Gene duplication; Penetrance; Medicine; Nerve conduction; Electrophysiology; Anatomy; Biology; Genetics; Phenotype; Internal medicine; Gene","score_opus":0.034001998940721596,"score_gpt":0.263754713376674,"score_spread":0.2297527144359524,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4398255835","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":[0.9822881,0.0013297785,0.001140491,0.0026636438,0.0003585502,0.00014752444,0.0005850124,0.00021837177,0.011268497],"genre_scores_gemma":[0.9957897,0.0004357748,0.0005867207,0.00053884217,0.00025839038,0.000024354465,0.00021265258,0.000032476815,0.0021210937],"study_design_codex":"case_report","study_design_gemma":"case_report","domain_scores_codex":[0.99969363,0.00002038452,0.000029469096,0.00013149547,0.000051317827,0.000073756295],"domain_scores_gemma":[0.99955314,0.00008111256,0.0000630166,0.000024800956,0.000046479625,0.00023137293],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00018360715,0.0019074623,0.0007566621,0.0020522245,0.0015555893,0.0006084351,0.00078708556,0.0033753081,0.0036729628],"category_scores_gemma":[0.001131849,0.00063262356,0.0005575959,0.00082311546,0.00082196726,0.00088188046,0.0008283988,0.0017301085,0.0011476814],"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":[0.00003480012,0.000017527944,0.0043659583,0.00001152069,0.0000034657191,0.9937232,0.000104185376,0.000053346015,0.00087680237,0.000066965345,0.00024415285,0.0004980934],"study_design_scores_gemma":[0.000017364886,0.00018793698,0.018785605,0.00001871899,0.000012519486,0.9789605,0.00013512524,0.0004408282,0.00046381122,0.0001900073,0.00076954096,0.000017970146],"about_ca_topic_score_codex":0.00540689,"about_ca_topic_score_gemma":0.0046875295,"teacher_disagreement_score":0.00540689,"about_ca_system_score_codex":0.0008869624,"about_ca_system_score_gemma":0.0007056611,"threshold_uncertainty_score":0.012287259},"labels":[],"label_agreement":null},{"id":"W4399284753","doi":"10.1101/2024.06.03.597092","title":"IP3 receptor depletion in a spontaneous canine model of Charcot-Marie-Tooth disease 1J with amelogenesis imperfecta","year":2024,"lang":"en","type":"preprint","venue":"bioRxiv (Cold Spring Harbor Laboratory)","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":false,"ca_institutions":"MaRS","funders":"","keywords":"Amelogenesis imperfecta; Tooth disease; Medicine; Orthodontics; Disease; Dentistry; Internal medicine; Enamel paint","score_opus":0.017992935506985823,"score_gpt":0.21220971482731155,"score_spread":0.19421677932032572,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4399284753","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":[0.99774194,0.000602883,0.000521073,0.0000952149,0.000037947153,0.000067538975,0.00024066234,0.00009243889,0.0006003834],"genre_scores_gemma":[0.9976362,0.0002501779,0.0005466965,0.00005916911,0.00001655521,0.00005280482,0.00028102595,0.000016267488,0.0011410748],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.999587,0.00007284052,0.000037428603,0.0001119372,0.00010121985,0.00008966392],"domain_scores_gemma":[0.9995939,0.000090587826,0.00013052586,0.00003215483,0.000025806474,0.00012707201],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00040828454,0.00071828405,0.000793221,0.0009989762,0.00058614323,0.00034554905,0.00045059272,0.0012503375,0.0014244954],"category_scores_gemma":[0.00032936488,0.0003804818,0.00045902122,0.00032151715,0.00082505116,0.00027540803,0.0003653653,0.00078333315,0.00037453434],"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":[0.0017514126,0.00073233346,0.0015287636,0.00012090372,0.000033528984,0.009398444,0.0001077617,0.00020359404,0.9840717,0.00024414607,0.00024624242,0.0015611979],"study_design_scores_gemma":[0.0013214156,0.023977188,0.10438054,0.00009949206,0.00042252144,0.122609004,0.0006815935,0.010859727,0.7217084,0.00063874386,0.013148119,0.00015328624],"about_ca_topic_score_codex":0.0011224065,"about_ca_topic_score_gemma":0.0014620417,"teacher_disagreement_score":0.0014244954,"about_ca_system_score_codex":0.0006307455,"about_ca_system_score_gemma":0.00028638597,"threshold_uncertainty_score":0.0047653913},"labels":[],"label_agreement":null},{"id":"W4399439583","doi":"10.1002/mds.29871","title":"<scp>MRI‐ARSACS</scp>: An Imaging Index for Autosomal Recessive Spastic Ataxia of Charlevoix‐Saguenay (<scp>ARSACS)</scp> Identification Based on the Multicenter <scp>PROSPAX</scp> Study","year":2024,"lang":"en","type":"article","venue":"Movement Disorders","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":6,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":true,"ca_institutions":"McGill University; Montreal Neurological Institute and Hospital","funders":"Deutsche Forschungsgemeinschaft","keywords":"Medicine; Magnetic resonance imaging; Receiver operating characteristic; Hereditary spastic paraplegia; Area under the curve; Pons; Spastic; Differential diagnosis; Internal medicine; Nuclear medicine; Pathology; Radiology; Genetics; Biology; Physical medicine and rehabilitation; Cerebral palsy; Phenotype","score_opus":0.02140263696428637,"score_gpt":0.2719833834323778,"score_spread":0.2505807464680915,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4399439583","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":[0.9994099,0.00016817059,0.00006531527,0.00000717821,0.0000020054208,0.000012215182,0.00014923305,0.0000029198327,0.00018304828],"genre_scores_gemma":[0.99910825,0.000051552142,0.00023516161,0.000005287116,0.000005446973,0.000013246266,0.0005041933,0.0000020973932,0.000074640004],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99964535,0.00009542111,0.000040733743,0.00011827528,0.00006593359,0.000034305307],"domain_scores_gemma":[0.99846673,0.0001963975,0.00070718164,0.00010328291,0.00027331527,0.0002532207],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0014483877,0.0005755611,0.0005089311,0.0015495856,0.00045584422,0.0005022115,0.00034714388,0.00042609047,0.0008966625],"category_scores_gemma":[0.0017496137,0.00016422255,0.0003769308,0.0005719856,0.00037425006,0.00028819978,0.00062812906,0.0002117246,0.00023641628],"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":[0.0005114119,0.000031831285,0.9960299,0.000015946218,0.00008556297,0.0001965269,0.00006230718,0.00007990557,0.0009901733,0.000013127164,0.00008525142,0.0018979672],"study_design_scores_gemma":[0.000018638537,0.00033033345,0.99789906,0.0000069328244,0.00004749116,0.0011104193,0.000047210644,0.00018599839,0.0001764312,0.000014106295,0.00015949253,0.0000037770872],"about_ca_topic_score_codex":0.0028304,"about_ca_topic_score_gemma":0.0030177946,"teacher_disagreement_score":0.0028304,"about_ca_system_score_codex":0.00040224163,"about_ca_system_score_gemma":0.0003280603,"threshold_uncertainty_score":0.007659912},"labels":[],"label_agreement":null},{"id":"W4399491890","doi":"10.3390/ijms25126378","title":"Compound Heterozygous Mutations of SACS in a Korean Cohort Study of Charcot-Marie-Tooth Disease Concurrent Cerebellar Ataxia and Spasticity","year":2024,"lang":"en","type":"article","venue":"International Journal of Molecular Sciences","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":4,"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":"Samsung Medical Center, Sungkyunkwan University; National Research Foundation of Korea; National Institute of Environmental Health Sciences; National Research Foundation","keywords":"Spasticity; Ataxia; Cerebellar ataxia; Medicine; Tooth disease; Compound heterozygosity; Cohort; Disease; Mutation; Genetics; Biology; Internal medicine; Physical medicine and rehabilitation; Gene; Psychiatry","score_opus":0.03065684485943338,"score_gpt":0.31337525777029646,"score_spread":0.2827184129108631,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4399491890","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":[0.9995889,0.000051370822,0.00006722572,0.000016439702,0.0000048413513,0.000012038721,0.00013838292,0.0000022326897,0.00011861888],"genre_scores_gemma":[0.99937844,0.000087630324,0.00011789194,0.00003110935,0.0000060582147,0.00000976201,0.00022335848,0.0000044671838,0.0001412891],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99963033,0.000041792806,0.00005522799,0.00016381296,0.000056922996,0.000051940013],"domain_scores_gemma":[0.9994886,0.000038478625,0.00011882129,0.000058766418,0.000089180205,0.00020627232],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00040396609,0.00079436926,0.0005109763,0.0009738388,0.001043647,0.0006006895,0.00039783158,0.00046831157,0.0017328284],"category_scores_gemma":[0.0009365817,0.00069081236,0.0005432304,0.0009095823,0.0003262236,0.00044163526,0.0007132881,0.00042197335,0.00031111462],"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":[0.0002881477,0.000114999246,0.9836541,0.000022021584,0.0001639466,0.0067945076,0.000677601,0.00007693974,0.0057547083,0.000084183244,0.00033624974,0.002032403],"study_design_scores_gemma":[0.00006373793,0.0003468851,0.9764118,0.000020969805,0.00022213373,0.019708939,0.001218674,0.00043116935,0.00054929755,0.00008219208,0.0009136661,0.000030414141],"about_ca_topic_score_codex":0.010809288,"about_ca_topic_score_gemma":0.011628028,"teacher_disagreement_score":0.010809288,"about_ca_system_score_codex":0.00034462378,"about_ca_system_score_gemma":0.0006471521,"threshold_uncertainty_score":0.02149278},"labels":[],"label_agreement":null},{"id":"W4399715676","doi":"10.1007/s00415-024-12505-y","title":"An MRI evaluation of white matter involvement in paradigmatic forms of spastic ataxia: results from the multi-center PROSPAX study","year":2024,"lang":"en","type":"article","venue":"Journal of Neurology","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":3,"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; Montreal Neurological Institute and Hospital","funders":"Deutsches Zentrum für Neurodegenerative Erkrankungen; Ministero della Salute; Deutsche Forschungsgemeinschaft; Eberhard Karls Universität Tübingen; Universitätsklinikum Essen; McGill University; Università degli Studi di Napoli Federico II","keywords":"White matter; Spastic; Hereditary spastic paraplegia; Diffusion MRI; Ataxia; Paraplegia; Medicine; Neurology; Neuroradiology; Neuroscience; Magnetic resonance imaging; Psychology; Physical medicine and rehabilitation; Radiology; Spinal cord; Biology","score_opus":0.08387219747531115,"score_gpt":0.33511565867982646,"score_spread":0.2512434612045153,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4399715676","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":[0.9991787,0.00019655515,0.00005771259,0.0000073993037,0.0000012576338,0.000015873295,0.0003224994,0.0000017755127,0.0002181647],"genre_scores_gemma":[0.9979778,0.00011173578,0.00026126212,0.000012587238,0.0000055879723,0.000020727826,0.0014779475,0.0000028407862,0.00012957722],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99948907,0.00017475687,0.00006841633,0.0001495218,0.00007613099,0.000042049982],"domain_scores_gemma":[0.9988876,0.00014542294,0.00043302673,0.00014673526,0.00023039256,0.00015676476],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0017357614,0.000495775,0.00049047597,0.0013393009,0.0005841965,0.00038115596,0.00030591627,0.00047395576,0.00081150274],"category_scores_gemma":[0.0015297324,0.00020756382,0.00032203837,0.000561578,0.00031771045,0.00034172056,0.0007121891,0.00019549568,0.000280301],"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":[0.0009657851,0.0000892235,0.9936626,0.000035259294,0.00017917746,0.00030245385,0.00017221489,0.00007148999,0.0014651282,0.000017785336,0.000103583225,0.002935341],"study_design_scores_gemma":[0.00002411603,0.00022009903,0.99866533,0.0000073444253,0.00004554527,0.000637268,0.000069693735,0.00005029881,0.00010119791,0.00001177644,0.00016357166,0.0000038420926],"about_ca_topic_score_codex":0.0030649346,"about_ca_topic_score_gemma":0.0056827134,"teacher_disagreement_score":0.0030649346,"about_ca_system_score_codex":0.00030899904,"about_ca_system_score_gemma":0.00027899726,"threshold_uncertainty_score":0.009179711},"labels":[],"label_agreement":null},{"id":"W4399817986","doi":"10.1515/9782760523937-013","title":"Sur Le Développement D’outils ThérapeutiquesIntégrant Le Tango","year":2009,"lang":"fr","type":"book-chapter","venue":"Presses de l'Université du Québec eBooks","topic":"Hereditary Neurological Disorders","field":"Neuroscience","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":"Ordre des Psychologues du Québec","funders":"","keywords":"INT; Political science; Philosophy; Computer science; Operating system","score_opus":0.030402437706181718,"score_gpt":0.20502954292826264,"score_spread":0.17462710522208091,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4399817986","genre_codex":"review","genre_gemma":"other","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"other","genre_consensus":null,"domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.036269717,0.5022802,0.009465904,0.036716733,0.0036897722,0.0001690785,0.00027995437,0.00026132632,0.41086745],"genre_scores_gemma":[0.19954626,0.31040388,0.01980118,0.013413846,0.001606585,0.0003405337,0.00033591798,0.00027208187,0.45427975],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.9996991,0.0001005873,0.000014475146,0.000026305132,0.000111622154,0.000047994356],"domain_scores_gemma":[0.9995259,0.0002648915,0.000033071945,0.000023104569,0.00009806391,0.00005496351],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0013464727,0.0005167043,0.00033000828,0.0009025554,0.0008683946,0.0017650628,0.0005123856,0.0008695762,0.0072776037],"category_scores_gemma":[0.0010611002,0.00014641887,0.00033647518,0.0005383531,0.0018372559,0.0011695052,0.0005157524,0.0014881131,0.0009066923],"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":[0.00023728835,0.00019129617,0.0011418102,0.0010600697,0.00005076817,0.0010303853,0.0042153895,0.000590402,0.0032067935,0.16115609,0.07475251,0.75236726],"study_design_scores_gemma":[0.000071058785,0.00015216811,0.0021578355,0.0010832531,0.00005337061,0.0014501751,0.00047272988,0.000284435,0.001463651,0.012639874,0.9801486,0.000022676237],"about_ca_topic_score_codex":0.051272247,"about_ca_topic_score_gemma":0.1155006,"teacher_disagreement_score":0.051272247,"about_ca_system_score_codex":0.004573962,"about_ca_system_score_gemma":0.0053517856,"threshold_uncertainty_score":0.101947606},"labels":[],"label_agreement":null},{"id":"W4400126526","doi":"10.1038/s41591-024-03078-4","title":"AAV gene therapy for hereditary spastic paraplegia type 50: a phase 1 trial in a single patient","year":2024,"lang":"en","type":"article","venue":"Nature Medicine","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":33,"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; SickKids Foundation; Hospital for Sick Children","funders":"Eunice Kennedy Shriver National Institute of Child Health and Human Development; Health Canada; Hospital for Sick Children","keywords":"Medicine; Hereditary spastic paraplegia; Genetic enhancement; Adverse effect; Tolerability; Clinical trial; Disease; Neutropenia; Intensive care medicine; Pediatrics; Internal medicine; Gene; Chemotherapy","score_opus":0.05653501108544415,"score_gpt":0.3475706825268508,"score_spread":0.29103567144140663,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4400126526","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":[0.98501647,0.003651282,0.00213309,0.0009779892,0.00019082567,0.003938439,0.0010945261,0.00015074277,0.0028467022],"genre_scores_gemma":[0.97885656,0.0034373875,0.004206328,0.0016572055,0.00017101002,0.00632621,0.001602279,0.000031652504,0.0037112953],"study_design_codex":"randomized_trial","study_design_gemma":"nonrandomized_trial","domain_scores_codex":[0.9996555,0.00015659093,0.000020525204,0.000051253126,0.00003964215,0.000076452474],"domain_scores_gemma":[0.999699,0.000076323224,0.00004960643,0.0000320794,0.000024225634,0.00011891354],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0016699241,0.00079722475,0.0011743843,0.00029573598,0.0003866039,0.0007990329,0.00040103422,0.0016136519,0.0030001083],"category_scores_gemma":[0.000815138,0.00022472684,0.0009341421,0.00024607655,0.0006498066,0.0005913478,0.00024806117,0.0013175826,0.00048421032],"study_design_candidate":"nonrandomized_trial","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":[0.4347478,0.07020951,0.0091242045,0.002102056,0.0027452095,0.0023913716,0.000943544,0.0057765623,0.1899415,0.0025985187,0.018108932,0.2613109],"study_design_scores_gemma":[0.35060155,0.6166787,0.009033241,0.00015943917,0.00067584624,0.0012900368,0.000115055904,0.002361519,0.008985826,0.001074979,0.008976537,0.000047166195],"about_ca_topic_score_codex":0.0008461439,"about_ca_topic_score_gemma":0.0020559232,"teacher_disagreement_score":0.0030001083,"about_ca_system_score_codex":0.0006049238,"about_ca_system_score_gemma":0.0011649394,"threshold_uncertainty_score":0.010036349},"labels":[],"label_agreement":null},{"id":"W4400140894","doi":"10.1093/brain/awae206","title":"A recurrent missense variant in <i>ITPR3</i> causes demyelinating Charcot-Marie-Tooth with variable severity","year":2024,"lang":"en","type":"article","venue":"Brain","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":3,"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 Institute of General Medical Sciences; Medical Research Council; National Institutes of Health; Medical Research Council Canada; Media Development Authority - Singapore; National Science and Technology Council; National Science Council; Wellcome Trust; University of Rochester; Muscular Dystrophy Association; Charcot-Marie-Tooth Association; University of Miami; Deutsche Forschungsgemeinschaft","keywords":"Missense mutation; Medicine; Tooth disease; Genetics; Biology; Mutation; Pathology; Disease; Gene","score_opus":0.027724168365511625,"score_gpt":0.2652262707649645,"score_spread":0.2375021023994529,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4400140894","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":[0.9981047,0.00020086169,0.00060520094,0.00005764132,0.000012815737,0.000016506045,0.000272887,0.00007814281,0.00065116654],"genre_scores_gemma":[0.9990427,0.00008215384,0.00031345035,0.000043641063,0.000019403114,0.0000053055533,0.00020649946,0.000016299124,0.00027048876],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.99979,0.000018411645,0.000021071202,0.00009383829,0.00004482869,0.00003187582],"domain_scores_gemma":[0.99980396,0.000044348977,0.00007719801,0.000015251185,0.0000162064,0.00004305166],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00015276106,0.00074283837,0.0003492556,0.00042205257,0.0003684108,0.00023519255,0.0003074835,0.0005378318,0.000982429],"category_scores_gemma":[0.000456651,0.00014312238,0.00039124594,0.00044047672,0.0003270569,0.000088495115,0.00029406702,0.00041283827,0.0003704784],"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":[0.0014052567,0.00033711042,0.14993514,0.0001806597,0.00041267628,0.28948936,0.0008055224,0.0006453748,0.5229859,0.0003822017,0.0024110184,0.031009829],"study_design_scores_gemma":[0.00011710762,0.0010889833,0.47952375,0.0000253582,0.00026399156,0.47841603,0.00017441364,0.001578821,0.035495285,0.00022957702,0.0030449713,0.0000417492],"about_ca_topic_score_codex":0.0016601582,"about_ca_topic_score_gemma":0.0015738725,"teacher_disagreement_score":0.0016601582,"about_ca_system_score_codex":0.00023951779,"about_ca_system_score_gemma":0.00013643633,"threshold_uncertainty_score":0.0033010244},"labels":[],"label_agreement":null},{"id":"W4400309111","doi":"10.1097/mao.0000000000004243","title":"Charcot–Marie–Tooth Disease and Hearing Loss: A Systematic Review With Meta-Analysis","year":2024,"lang":"en","type":"review","venue":"Otology & Neurotology","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":2,"is_retracted":false,"has_abstract":true,"route_ca_aff":false,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":true,"ca_institutions":"","funders":"","keywords":"Medicine; Hearing loss; Meta-analysis; Tooth disease; Tooth loss; Audiology; MEDLINE; Disease; Dentistry; Pathology; Oral health","score_opus":0.16412469300651283,"score_gpt":0.36591071468985004,"score_spread":0.2017860216833372,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4400309111","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":[0.00446673,0.9938154,0.0003329145,0.00018841465,0.00009159996,0.00029159474,0.00061437424,0.000017094213,0.0001819089],"genre_scores_gemma":[0.13518366,0.8589412,0.0022664976,0.00067256036,0.00023057238,0.0015707043,0.0008541297,0.00002114706,0.0002594705],"study_design_codex":"systematic_review","study_design_gemma":"meta_analysis","domain_scores_codex":[0.9931623,0.0026690883,0.0022024927,0.00085136475,0.0008396833,0.00027510463],"domain_scores_gemma":[0.98300743,0.011991188,0.0030850945,0.0004139951,0.0012747077,0.00022753885],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.009360744,0.0022043502,0.016780714,0.008445299,0.00069091405,0.002856288,0.0021185402,0.0018814157,0.0039316374],"category_scores_gemma":[0.025638502,0.0011964348,0.022032522,0.01062211,0.0005839143,0.0017161629,0.0014581679,0.0011375726,0.0002754876],"study_design_candidate":"meta_analysis","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":[0.0011654216,0.000030783078,0.0055413325,0.6002428,0.37812528,0.00021191564,0.00010637532,0.00036861678,0.00024341495,0.00012169118,0.0008179244,0.013024446],"study_design_scores_gemma":[0.00044183774,0.0002223103,0.0068284697,0.066231534,0.9233662,0.00020731955,0.00008457201,0.00015931376,0.00009852849,0.00016685066,0.0021647017,0.000028420021],"about_ca_topic_score_codex":0.006886148,"about_ca_topic_score_gemma":0.016227044,"teacher_disagreement_score":0.016780714,"about_ca_system_score_codex":0.0023176034,"about_ca_system_score_gemma":0.0041173995,"threshold_uncertainty_score":0.049504936},"labels":[],"label_agreement":null},{"id":"W4400477775","doi":"10.14802/jmd.24054","title":"Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay Masquerading as Charcot-Marie-Tooth Disease: A Case Study and Literature Review of Korean Patients","year":2024,"lang":"en","type":"article","venue":"Journal of Movement Disorders","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":1,"is_retracted":false,"has_abstract":true,"route_ca_aff":false,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":true,"ca_institutions":"","funders":"","keywords":"Medicine; Tooth disease; Ataxia; Dermatology; Disease; Pediatrics; Pathology; Psychiatry","score_opus":0.014369694684314914,"score_gpt":0.2740079888973913,"score_spread":0.2596382942130764,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4400477775","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":[0.93242216,0.055395275,0.0025191042,0.0008051402,0.00022814565,0.00031773123,0.00081109174,0.000093693416,0.007407548],"genre_scores_gemma":[0.95339173,0.04058153,0.0020689112,0.0006116997,0.00040291157,0.00008095141,0.00068954605,0.000031989846,0.0021406626],"study_design_codex":"case_report","study_design_gemma":"case_report","domain_scores_codex":[0.99947447,0.000033736647,0.00018374049,0.00015221832,0.00007276886,0.000083123996],"domain_scores_gemma":[0.9995265,0.00008961866,0.00016765995,0.000030323168,0.00006933084,0.000116528616],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00037340474,0.0012784762,0.0010435574,0.0042080884,0.0014388518,0.001237875,0.0009600834,0.0014690197,0.002730158],"category_scores_gemma":[0.00071960123,0.0007615587,0.0008641741,0.0036627601,0.00086275407,0.001858189,0.0010487206,0.0005551642,0.00081872236],"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":[0.00009306683,0.0001698743,0.052891232,0.00063541404,0.00010467219,0.9224499,0.0013541041,0.00011224868,0.0054749483,0.00027713412,0.0015263454,0.014911072],"study_design_scores_gemma":[0.0000124158805,0.00004100202,0.021800844,0.00014344246,0.00016727523,0.9719596,0.0008341445,0.00010528075,0.0006160479,0.00011618474,0.0041697626,0.000033983728],"about_ca_topic_score_codex":0.0024525777,"about_ca_topic_score_gemma":0.003948183,"teacher_disagreement_score":0.0042080884,"about_ca_system_score_codex":0.0006053001,"about_ca_system_score_gemma":0.00076513004,"threshold_uncertainty_score":0.009133279},"labels":[],"label_agreement":null},{"id":"W4402106390","doi":"10.1016/j.jaad.2024.07.1131","title":"50376 Prevalence and Clinical Correlates of Apathy in Psoriatic Disease","year":2024,"lang":"en","type":"article","venue":"Journal of the American Academy of Dermatology","topic":"Hereditary Neurological Disorders","field":"Neuroscience","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":"University of British Columbia; University of Alberta","funders":"","keywords":"Medicine; Apathy; Dermatology; Epidemiology; Disease; Internal medicine","score_opus":0.030915832111147123,"score_gpt":0.34577194889930857,"score_spread":0.31485611678816144,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4402106390","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":[0.99815327,0.0003014035,0.000028034918,0.00003081389,0.000004845429,0.00000495529,0.00016223562,0.0000030459762,0.0013114314],"genre_scores_gemma":[0.99962616,0.000086066124,0.000029970908,0.000012420151,0.000010020058,0.000002348009,0.00009612997,9.0004136e-7,0.00013591204],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99961084,0.00008232506,0.000068707144,0.00006259922,0.00010998056,0.000065517685],"domain_scores_gemma":[0.9985091,0.00027301503,0.00069100445,0.000050852756,0.00019499952,0.00028099163],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00026124634,0.00022416808,0.00028942674,0.0018756177,0.0006285,0.0007533492,0.00028333472,0.00045888446,0.0047559673],"category_scores_gemma":[0.0024383236,0.00024899264,0.00022201063,0.0015245025,0.00033397437,0.00051062426,0.00045066688,0.00042306428,0.00057174684],"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":[0.00011021994,0.000049818507,0.9976801,0.00000804221,0.000016546293,0.00029752144,0.000052289368,0.00000938555,0.0004449762,0.000013975364,0.000045287867,0.0012718199],"study_design_scores_gemma":[0.0000032764165,0.000057241836,0.99823844,0.0000037466416,0.000008817317,0.0013744718,0.00015571553,0.000042097337,0.000034654226,0.000018722136,0.000060297913,0.0000023938428],"about_ca_topic_score_codex":0.0029257038,"about_ca_topic_score_gemma":0.0030598466,"teacher_disagreement_score":0.0047559673,"about_ca_system_score_codex":0.00020513692,"about_ca_system_score_gemma":0.00022118914,"threshold_uncertainty_score":0.015910327},"labels":[],"label_agreement":null},{"id":"W4402309714","doi":"10.4103/aian.aian_280_24","title":"A Case of Facial-Onset Sensory Motor Neuronopathy – A Rare Variant of Motor Neuron Disease","year":2024,"lang":"en","type":"article","venue":"Annals of Indian Academy of Neurology","topic":"Hereditary Neurological Disorders","field":"Neuroscience","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; Motor neuron; Sensory system; Disease; Physical medicine and rehabilitation; Neuroscience; Pathology; Psychology","score_opus":0.08513298064966342,"score_gpt":0.32757645149027526,"score_spread":0.24244347084061185,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4402309714","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":[0.9890564,0.0015648156,0.0011404705,0.0005798273,0.000104959865,0.000060012062,0.00014045101,0.000075984506,0.0072770696],"genre_scores_gemma":[0.9981505,0.0003089857,0.00050687644,0.00015033019,0.00011686878,0.000012761297,0.00005125294,0.000008034169,0.00069434225],"study_design_codex":"case_report","study_design_gemma":"case_report","domain_scores_codex":[0.9995889,0.000037708738,0.00003944906,0.00011786866,0.000054096006,0.00016196327],"domain_scores_gemma":[0.99944633,0.00013143261,0.0001489733,0.000076129196,0.000045932997,0.00015120026],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00017168872,0.0011947043,0.0006114035,0.0009557473,0.0013387895,0.0010287513,0.00079235225,0.0026562295,0.0018017079],"category_scores_gemma":[0.0014951271,0.00058332074,0.00051460235,0.0008344686,0.0012510403,0.0010743083,0.0010865083,0.001211401,0.00043272038],"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":[0.000029381055,0.000021190493,0.007448328,0.000024211222,0.000006916735,0.98916656,0.00012089344,0.00006535222,0.0016316624,0.00019892669,0.00015514086,0.0011314257],"study_design_scores_gemma":[0.000007315903,0.00003412722,0.0052279145,0.000006656049,0.0000052392415,0.9938018,0.00008608046,0.00016334717,0.00024030775,0.0001240087,0.00029852445,0.0000047858857],"about_ca_topic_score_codex":0.002615507,"about_ca_topic_score_gemma":0.0032979427,"teacher_disagreement_score":0.0026562295,"about_ca_system_score_codex":0.00086950243,"about_ca_system_score_gemma":0.00049704954,"threshold_uncertainty_score":0.006308675},"labels":[],"label_agreement":null},{"id":"W4403035922","doi":"10.1002/iub.2918","title":"Characterization of a novel heterozygous variant in the histidyl‐<scp>tRNA</scp> synthetase gene associated with <scp>Charcot–Marie–Tooth</scp> disease type <scp>2W</scp>","year":2024,"lang":"en","type":"article","venue":"IUBMB Life","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":8,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Children’s Health Research Institute; Western University","funders":"Institute of Genetics; Ontario Ministry of Research and Innovation; Natural Sciences and Engineering Research Council of Canada; Canadian Network for Research and Innovation in Machining Technology, Natural Sciences and Engineering Research Council of Canada","keywords":"Gene; Recombinant DNA; Tooth disease; Biology; Yeast; Saccharomyces cerevisiae; Histidine; Transfer RNA; Genetics; Molecular biology; Enzyme; Biochemistry; RNA","score_opus":0.03517910441808104,"score_gpt":0.2435476762824298,"score_spread":0.20836857186434876,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4403035922","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":[0.99762386,0.00019600819,0.00095799,0.00017376662,0.0000364843,0.000035374716,0.00025208088,0.000032236672,0.00069216057],"genre_scores_gemma":[0.99813676,0.000089303336,0.0008052292,0.0000908286,0.000023355386,0.000010914269,0.00017079238,0.000015693602,0.0006571895],"study_design_codex":"case_report","study_design_gemma":"observational","domain_scores_codex":[0.9998179,0.000014584343,0.000019746883,0.00007312814,0.00004399326,0.00003066904],"domain_scores_gemma":[0.9996581,0.00010663653,0.00007641004,0.000017139144,0.000029392748,0.00011229106],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.000131683,0.00084254803,0.00052899774,0.0007250185,0.00043883087,0.0003553224,0.00045200402,0.0012608147,0.001707057],"category_scores_gemma":[0.0006053203,0.00021686018,0.00042057564,0.00042930892,0.0005634036,0.00017958037,0.0004626199,0.00058987294,0.00036807905],"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":[0.00040644576,0.0001800447,0.018571168,0.00009985748,0.00007025168,0.7358355,0.00075542793,0.00037341815,0.23584634,0.00044707648,0.0003749941,0.0070394254],"study_design_scores_gemma":[0.00011140061,0.0010442553,0.10254998,0.000040349554,0.00012072718,0.8371626,0.00045247722,0.0021679364,0.053071026,0.0005399797,0.0026724166,0.00006690322],"about_ca_topic_score_codex":0.0018807556,"about_ca_topic_score_gemma":0.0016955207,"teacher_disagreement_score":0.0018807556,"about_ca_system_score_codex":0.000268895,"about_ca_system_score_gemma":0.00025282375,"threshold_uncertainty_score":0.0057106614},"labels":[],"label_agreement":null},{"id":"W4403164364","doi":"10.1101/2024.10.04.24314535","title":"Genetic Risk of Axonal Neuropathy Following Infection","year":2024,"lang":"en","type":"preprint","venue":"medRxiv","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":false,"ca_institutions":"Children's Hospital of Eastern Ontario","funders":"National Institute for Health and Care Research","keywords":"Medicine; Neuroscience; Biology","score_opus":0.03201586709207864,"score_gpt":0.26814014217727256,"score_spread":0.2361242750851939,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4403164364","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":[0.99830425,0.00031135642,0.0002519905,0.000081033,0.000006337753,0.00000849769,0.0001590473,0.000015436452,0.00086210825],"genre_scores_gemma":[0.9991417,0.00016719678,0.00019603384,0.000034413064,0.000013200779,0.0000054963525,0.00013729619,0.0000038899298,0.00030070115],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99980587,0.00004360203,0.000016446627,0.0000602451,0.000028163295,0.00004570874],"domain_scores_gemma":[0.9995821,0.00010166349,0.00015158365,0.000021530977,0.00004136718,0.000101798054],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00015618939,0.0005724088,0.0002983294,0.0005189266,0.00050980435,0.00035900963,0.00022206333,0.0007272373,0.0043019936],"category_scores_gemma":[0.00074729376,0.000111425696,0.0001942424,0.00045342938,0.00026117737,0.00018767659,0.00035165594,0.000380385,0.00036770923],"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":[0.00056170893,0.00013816706,0.9392124,0.00009436654,0.00011715803,0.018693088,0.00036217817,0.00026699994,0.027484803,0.00048531347,0.0006803832,0.011903372],"study_design_scores_gemma":[0.000018876275,0.0005380746,0.9361334,0.000072130584,0.00009748412,0.057133056,0.00046626048,0.00058918924,0.0031364146,0.00054200063,0.0012427744,0.00003037997],"about_ca_topic_score_codex":0.0012666356,"about_ca_topic_score_gemma":0.00059952616,"teacher_disagreement_score":0.0043019936,"about_ca_system_score_codex":0.000150127,"about_ca_system_score_gemma":0.00014394466,"threshold_uncertainty_score":0.014391601},"labels":[],"label_agreement":null},{"id":"W4403283158","doi":"10.1016/j.jics.2024.101403","title":"In silico identification and virtual screening to discover potent therapeutic phytochemicals against CMT2A","year":2024,"lang":"en","type":"article","venue":"Journal of the Indian Chemical Society","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":4,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Université Laval","funders":"King Saud University","keywords":"In silico; Chemistry; Identification (biology); Virtual screening; Computational biology; Biochemistry; Drug discovery; Gene; Ecology","score_opus":0.020963401419951153,"score_gpt":0.2730753820867917,"score_spread":0.25211198066684054,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4403283158","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":[0.9193522,0.011720525,0.033175696,0.00084036856,0.00020677019,0.00070692773,0.007672739,0.0024815865,0.023843164],"genre_scores_gemma":[0.94916123,0.004627372,0.036208216,0.00022284269,0.000026486363,0.00022886902,0.0057758484,0.000087136716,0.0036619988],"study_design_codex":"simulation_or_modeling","study_design_gemma":"simulation_or_modeling","domain_scores_codex":[0.99981636,0.000046234978,0.000009350358,0.00003281541,0.000054811902,0.00004048979],"domain_scores_gemma":[0.9998721,0.000072185365,0.000014780468,0.000008126757,0.000017557646,0.000015255817],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00039281973,0.0010011232,0.0014460414,0.0008891959,0.00051371014,0.0011297017,0.00085102697,0.0004939601,0.0046882886],"category_scores_gemma":[0.0005547643,0.00034211433,0.0016371858,0.0008006327,0.0002071194,0.00040682647,0.0004672588,0.0007472236,0.0007518905],"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":[0.0065720216,0.0049315905,0.01729076,0.0073389583,0.0024099448,0.0029673176,0.0003122115,0.4770886,0.2964468,0.01293116,0.014097069,0.1576136],"study_design_scores_gemma":[0.0012107365,0.0047322665,0.005313075,0.0002095696,0.002651492,0.0011879575,0.00027654722,0.8470634,0.1008063,0.0039521903,0.03246997,0.00012650284],"about_ca_topic_score_codex":0.001636504,"about_ca_topic_score_gemma":0.003748936,"teacher_disagreement_score":0.0046882886,"about_ca_system_score_codex":0.0003832021,"about_ca_system_score_gemma":0.0009261315,"threshold_uncertainty_score":0.01568389},"labels":[],"label_agreement":null},{"id":"W4403551464","doi":"10.1111/pde.15784","title":"Congenital Insensitivity to Pain With Anhidrosis Is Associated With Harlequin Color Change: A Survey Study","year":2024,"lang":"en","type":"article","venue":"Pediatric Dermatology","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":1,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of British Columbia","funders":"","keywords":"Anhidrosis; Medicine; Sensation; Dermatology; Disease; Pediatrics; Pathology; Neuroscience","score_opus":0.06678031887173606,"score_gpt":0.2815019238554142,"score_spread":0.21472160498367815,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4403551464","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":[0.9993236,0.00007835136,0.00006623152,0.000016913189,0.0000015766742,0.00000858697,0.00012170937,0.0000012581353,0.00038179054],"genre_scores_gemma":[0.99936,0.00019048275,0.00011463072,0.000029517729,0.0000029662338,0.000010521951,0.00012875772,0.0000011585404,0.0001618678],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9995384,0.00013093726,0.00007014424,0.000092562324,0.00009747892,0.00007039702],"domain_scores_gemma":[0.9989801,0.00018385304,0.00034637089,0.00005210675,0.00022817362,0.00020928028],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00049838435,0.00013936206,0.0002161546,0.001036502,0.0003357804,0.00040240987,0.00016388188,0.00028798362,0.0011385579],"category_scores_gemma":[0.0013976224,0.00016275613,0.00021286421,0.00090031326,0.0001872344,0.00043812848,0.0003672314,0.0002749966,0.0002346165],"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":[0.000008169092,0.000034092787,0.9975702,0.00001223953,0.000010502505,0.00031883174,0.00059929484,0.000009316717,0.00022047434,0.000011100676,0.00006210722,0.001143718],"study_design_scores_gemma":[7.362119e-7,0.0001331221,0.99573493,0.000008014772,0.000011360565,0.0016047294,0.0020177325,0.000060150418,0.00006254093,0.000007646597,0.00035504674,0.0000040413106],"about_ca_topic_score_codex":0.0055072946,"about_ca_topic_score_gemma":0.006629192,"teacher_disagreement_score":0.0055072946,"about_ca_system_score_codex":0.00023349667,"about_ca_system_score_gemma":0.0002641721,"threshold_uncertainty_score":0.010950446},"labels":[],"label_agreement":null},{"id":"W4403850544","doi":"10.1007/s43678-024-00798-x","title":"Isolated leg weakness with painful spasms in an adolescent","year":2024,"lang":"en","type":"article","venue":"Canadian Journal of Emergency Medicine","topic":"Hereditary Neurological Disorders","field":"Neuroscience","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":"London Health Sciences Centre; Western University","funders":"","keywords":"Medicine; Weakness; Physical medicine and rehabilitation; Physical therapy; Surgery","score_opus":0.11046874909452728,"score_gpt":0.33027636461532905,"score_spread":0.21980761552080177,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4403850544","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":[0.99030906,0.00078841596,0.00045530795,0.0012729443,0.00013450332,0.000086278305,0.00010227165,0.000032547105,0.0068186247],"genre_scores_gemma":[0.9979011,0.0003847792,0.00030058052,0.00039318262,0.00015312366,0.000011972681,0.00004456492,0.000007946856,0.0008028455],"study_design_codex":"case_report","study_design_gemma":"case_report","domain_scores_codex":[0.99958533,0.00003800907,0.000043852262,0.000069430396,0.00007520709,0.00018825053],"domain_scores_gemma":[0.99903095,0.00021924885,0.00020821451,0.00002257776,0.00008702282,0.000431977],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0002367095,0.0013781368,0.00091437146,0.0018379391,0.00179697,0.00080627145,0.0011361262,0.0030786712,0.0040233876],"category_scores_gemma":[0.002291171,0.00066711,0.00073395396,0.00080798037,0.0012074779,0.0010087836,0.0010482705,0.0024309037,0.0006003993],"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":[0.000028850569,0.000103683764,0.024418034,0.000022021108,0.0000074244977,0.9737664,0.00013992203,0.000042324922,0.00038379044,0.00011850953,0.00017758926,0.0007914199],"study_design_scores_gemma":[0.000021816626,0.00018214111,0.047156695,0.000033238728,0.000020418116,0.95147103,0.0003663852,0.0002335945,0.00018850066,0.00010232773,0.0002137325,0.000010204545],"about_ca_topic_score_codex":0.008250167,"about_ca_topic_score_gemma":0.013981516,"teacher_disagreement_score":0.008250167,"about_ca_system_score_codex":0.0013090719,"about_ca_system_score_gemma":0.0012790291,"threshold_uncertainty_score":0.01640433},"labels":[],"label_agreement":null},{"id":"W4404183234","doi":"10.1136/jnnp-2024-abn.7","title":"A UK wide research registry for inherited peripheral neuropathy","year":2024,"lang":"en","type":"article","venue":"","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":false,"ca_institutions":"St. Thomas Hospital","funders":"","keywords":"Peripheral neuropathy; Peripheral; Medicine; Computer science; Internal medicine","score_opus":0.17061498605760975,"score_gpt":0.39173785652942256,"score_spread":0.2211228704718128,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4404183234","genre_codex":"dataset","genre_gemma":"other","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"other","genre_consensus":null,"domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.114029996,0.020968344,0.012308757,0.009114855,0.0017986511,0.0097339405,0.6885637,0.0018493014,0.14163242],"genre_scores_gemma":[0.24695134,0.021379057,0.027910136,0.0056713126,0.0011482821,0.016741559,0.61070454,0.0008804549,0.06861332],"study_design_codex":"not_applicable","study_design_gemma":"not_applicable","domain_scores_codex":[0.994263,0.0010865682,0.0019341598,0.0011854031,0.001166377,0.0003643481],"domain_scores_gemma":[0.97454786,0.0030252738,0.0067723864,0.004149506,0.007906438,0.0035985163],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0033361823,0.0005573037,0.0013345903,0.004832718,0.0008756875,0.0016541012,0.0014741648,0.0012951246,0.05486366],"category_scores_gemma":[0.020616122,0.00050794444,0.0005879183,0.007046752,0.00035273863,0.00190283,0.0031675142,0.001077498,0.020446349],"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":[0.0014644746,0.00017148888,0.095826425,0.004933358,0.00024911945,0.0024991077,0.001498204,0.0002478587,0.0015399448,0.0065750005,0.7671697,0.11782526],"study_design_scores_gemma":[0.00076816004,0.00050024706,0.35934713,0.0050370465,0.00031364744,0.006570659,0.0009818707,0.00057076965,0.00061541627,0.001517264,0.6236001,0.0001776332],"about_ca_topic_score_codex":0.018790025,"about_ca_topic_score_gemma":0.020428874,"teacher_disagreement_score":0.05486366,"about_ca_system_score_codex":0.0018976398,"about_ca_system_score_gemma":0.0057229893,"threshold_uncertainty_score":0.18353724},"labels":[],"label_agreement":null},{"id":"W4404784290","doi":"10.1101/2024.11.27.625322","title":"Engineered CRISPR-Base Editors as a Permanent Treatment for Familial Dysautonomia","year":2024,"lang":"en","type":"preprint","venue":"bioRxiv (Cold Spring Harbor Laboratory)","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":3,"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; York University; Ögonfonden; Charles A. King Trust; Massachusetts General Hospital; Dysautonomia Foundation","keywords":"Familial dysautonomia; CRISPR; Dysautonomia; Medicine; Genetics; Biology; Disease; Internal medicine","score_opus":0.02675574521587842,"score_gpt":0.25236661332202004,"score_spread":0.22561086810614162,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4404784290","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":[0.88173014,0.0053108553,0.100109175,0.0007307815,0.0006855616,0.0002410933,0.001128778,0.0027372586,0.007326359],"genre_scores_gemma":[0.9588426,0.0015095985,0.031626943,0.0002017864,0.00005405229,0.00009878049,0.00052101456,0.00020396494,0.006941319],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99981314,0.00002688359,0.000014328155,0.000050302428,0.000069930655,0.000025436178],"domain_scores_gemma":[0.99992645,0.000017707642,0.000022801969,0.000011073236,0.000006858685,0.0000151051245],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00020656739,0.00038149828,0.00036768473,0.00027016163,0.00015515447,0.00032660514,0.00029521258,0.00045928272,0.0012863777],"category_scores_gemma":[0.0001571107,0.00014466843,0.0002386584,0.0000915798,0.00023658405,0.00016784485,0.00025781043,0.0007887122,0.0003220267],"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":[0.000120020944,0.00005521566,0.00010349275,0.00006681726,0.000022074733,0.00022620593,0.000015209321,0.00028182755,0.9907318,0.00058945536,0.00041003517,0.0073779095],"study_design_scores_gemma":[0.00003680379,0.00038735868,0.0004695158,0.0000073876863,0.00002714971,0.0009557743,0.00000871164,0.0013701498,0.98863703,0.00013375668,0.007957349,0.000009127134],"about_ca_topic_score_codex":0.00025233033,"about_ca_topic_score_gemma":0.00042135053,"teacher_disagreement_score":0.0012863777,"about_ca_system_score_codex":0.00018020885,"about_ca_system_score_gemma":0.00012069336,"threshold_uncertainty_score":0.0043033957},"labels":[],"label_agreement":null},{"id":"W4404824279","doi":"10.1007/s10048-024-00789-1","title":"Three Iranian patients with rare subtypes of hereditary spastic paraplegia (HSP): SPG76, SPG56, and SPG69","year":2024,"lang":"en","type":"article","venue":"Neurogenetics","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":2,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Centre Hospitalier Universitaire Sainte-Justine","funders":"University of Social Welfare and Rehabilitation Sciences","keywords":"Hereditary spastic paraplegia; Human genetics; Spastic; Medicine; Molecular medicine; Genetics; Biology; Internal medicine; Physical therapy; Phenotype; Gene; Cerebral palsy","score_opus":0.017218432397927745,"score_gpt":0.21748865596344027,"score_spread":0.20027022356551252,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4404824279","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":[0.997652,0.00013434068,0.0003414503,0.00018385358,0.000034146837,0.000042841653,0.00006079604,0.000009565977,0.0015410418],"genre_scores_gemma":[0.998838,0.00009287578,0.0002984861,0.00014917325,0.000045520577,0.000014994925,0.000082649,0.000005375379,0.00047293413],"study_design_codex":"case_report","study_design_gemma":"case_report","domain_scores_codex":[0.9997019,0.000025898002,0.000048566715,0.00008049316,0.00004282337,0.00010027247],"domain_scores_gemma":[0.9995751,0.00009840563,0.00009321043,0.000041710624,0.000055555665,0.00013612535],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00019619144,0.0015246941,0.0006261658,0.0008540213,0.002350863,0.00068388844,0.0006435387,0.0012226286,0.0020979673],"category_scores_gemma":[0.0014770608,0.00046715388,0.0007685591,0.0009429128,0.0013183018,0.00039609158,0.0009966305,0.00079835666,0.00029301617],"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":[0.00065223913,0.00040214302,0.21475706,0.00008273198,0.000104731145,0.7595507,0.004641574,0.00026401368,0.00915496,0.0012527052,0.0007528477,0.008384262],"study_design_scores_gemma":[0.0001980667,0.0005669538,0.18491952,0.00003278851,0.00015675602,0.803133,0.004024041,0.00042896435,0.0022470704,0.0011761187,0.0030441536,0.00007261211],"about_ca_topic_score_codex":0.0049093408,"about_ca_topic_score_gemma":0.0046041515,"teacher_disagreement_score":0.0049093408,"about_ca_system_score_codex":0.0007752462,"about_ca_system_score_gemma":0.00066526816,"threshold_uncertainty_score":0.009761512},"labels":[],"label_agreement":null},{"id":"W4405424256","doi":"10.1007/s00415-024-12744-z","title":"Giant axonal neuropathy (GAN): cross-sectional data on phenotypes, genotypes, and proteomic signature from a German cohort","year":2024,"lang":"en","type":"article","venue":"Journal of Neurology","topic":"Hereditary Neurological Disorders","field":"Neuroscience","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":"Children's Hospital of Eastern Ontario","funders":"European Regional Development Fund; Universitätsklinikum Essen","keywords":"Neurology; Cohort; Biology; Phenotype; Disease; Peripheral neuropathy; Genotype; Epidemiology; Abnormality; Bioinformatics; Genetics; Neuroscience; Medicine; Gene; Pathology; Endocrinology; Diabetes mellitus; Psychiatry","score_opus":0.04140669625304364,"score_gpt":0.310203284024594,"score_spread":0.26879658777155035,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4405424256","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":[0.99917847,0.00011164064,0.00009576865,0.000012112094,0.0000018131731,0.0000075291314,0.00038504897,0.000002654338,0.00020494808],"genre_scores_gemma":[0.998938,0.00010975372,0.00008617396,0.000023258395,0.0000034130956,0.00000955078,0.0007035162,0.0000031777101,0.000123149],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99963653,0.000068296096,0.000038416627,0.00015846295,0.00004626291,0.000052145013],"domain_scores_gemma":[0.9996226,0.00005321018,0.00011372754,0.000058359918,0.00005074272,0.00010141834],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00040721486,0.0004370373,0.00034561002,0.0009944234,0.00043382501,0.000426073,0.0002316513,0.00035740327,0.0013384612],"category_scores_gemma":[0.00072950893,0.00025265917,0.00027529223,0.00086399843,0.00031946113,0.00034581288,0.00063132227,0.00018167672,0.0003314685],"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":[0.00010493493,0.000034624394,0.9956392,0.000014819515,0.00009151435,0.00047544987,0.00026806755,0.00003842962,0.0013460875,0.000029213139,0.00016315005,0.0017944677],"study_design_scores_gemma":[0.0000042420156,0.00007413813,0.9985306,0.000003478111,0.000036571342,0.00074908463,0.00021021164,0.000041988555,0.00006847664,0.0000176514,0.00025999194,0.0000035213325],"about_ca_topic_score_codex":0.004103106,"about_ca_topic_score_gemma":0.0044386997,"teacher_disagreement_score":0.004103106,"about_ca_system_score_codex":0.00026045225,"about_ca_system_score_gemma":0.00020522477,"threshold_uncertainty_score":0.008158445},"labels":[],"label_agreement":null},{"id":"W4405586347","doi":"10.1111/1346-8138.17572","title":"Traumatic experiences, dissociative symptoms, and alexithymia in patients with alopecia areata","year":2024,"lang":"en","type":"article","venue":"The Journal of Dermatology","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":1,"is_retracted":false,"has_abstract":true,"route_ca_aff":false,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":true,"ca_institutions":"","funders":"","keywords":"Alexithymia; CTQ tree; Toronto Alexithymia Scale; Dissociative Experiences Scale; Alopecia areata; Neglect; Dissociative; Clinical psychology; Psychology; Psychological abuse; Psychiatry; Dissociative disorders; Medicine; Sexual abuse; Dermatology; Poison control; Injury prevention; Cognition; Domestic violence","score_opus":0.014672819542242685,"score_gpt":0.24460748663989582,"score_spread":0.22993466709765314,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4405586347","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":[0.999724,0.0001089592,0.000013581902,0.000009518398,0.0000018651576,0.0000025775553,0.000010265922,7.240341e-7,0.000128467],"genre_scores_gemma":[0.99985135,0.000060928265,0.000018098222,0.000007974074,0.000004162039,0.0000019172705,0.000021650678,1.9403434e-7,0.00003376418],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99974376,0.00006814759,0.000039734903,0.000042136537,0.000059621347,0.00004671408],"domain_scores_gemma":[0.9993206,0.00013534182,0.00035190152,0.000027555554,0.000038584225,0.00012600073],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00024289267,0.00022272512,0.00034117416,0.00083710277,0.0005248439,0.00044623477,0.00014398433,0.00032019996,0.0013033424],"category_scores_gemma":[0.0016077529,0.00022448935,0.00022654947,0.000506934,0.00038112965,0.00031818697,0.00046212363,0.00036626926,0.00012697885],"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":[0.0002520726,0.000086387656,0.9934962,0.000019667908,0.000041730862,0.001364131,0.00051785976,0.000029645758,0.0011790717,0.000016986924,0.000042858042,0.0029533675],"study_design_scores_gemma":[0.000011318421,0.00021235351,0.99513876,0.000005308739,0.000014821943,0.0038803415,0.0005624284,0.00004491575,0.000056332676,0.000016051732,0.000054195534,0.0000031973457],"about_ca_topic_score_codex":0.0010085694,"about_ca_topic_score_gemma":0.0010324351,"teacher_disagreement_score":0.0013033424,"about_ca_system_score_codex":0.00015299415,"about_ca_system_score_gemma":0.00011978198,"threshold_uncertainty_score":0.0043601394},"labels":[],"label_agreement":null},{"id":"W4405854006","doi":"10.1111/ene.70025","title":"From spastic paraplegia to infantile neurodegenerative disorder: Expanding the phenotypic spectrum associated with biallelic <scp><i>SPAST</i></scp> variants","year":2024,"lang":"en","type":"article","venue":"European Journal of Neurology","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":6,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Alberta; McGill University; Montreal Neurological Institute and Hospital","funders":"Eunice Kennedy Shriver National Institute of Child Health and Human Development; Canadian Institutes of Health Research; National Institutes of Health","keywords":"Hereditary spastic paraplegia; Medicine; Exome sequencing; Sanger sequencing; Genetic heterogeneity; Compound heterozygosity; Genetics; Spastic quadriplegia; Phenotype; Pediatrics; Bioinformatics; Mutation; Gene; Biology; Physical medicine and rehabilitation","score_opus":0.022042988708079594,"score_gpt":0.24062437303486217,"score_spread":0.2185813843267826,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4405854006","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":[0.9966396,0.0005978462,0.00053501636,0.000111861074,0.000007322415,0.000015177636,0.00008649083,0.00003430159,0.0019722923],"genre_scores_gemma":[0.99860543,0.0003182787,0.00053157005,0.000110718036,0.000025868854,0.0000080723075,0.00013355743,0.000012151065,0.0002544239],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99981576,0.000033127188,0.000029475761,0.00004638325,0.000027775553,0.000047602396],"domain_scores_gemma":[0.99967134,0.000091544025,0.00008516346,0.000020370537,0.000046236077,0.000085287735],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00019592223,0.0011198785,0.00043535203,0.00085033645,0.00036271123,0.00026100187,0.00022429593,0.00042177868,0.0026176288],"category_scores_gemma":[0.00075069984,0.00017289999,0.00021608805,0.0004821295,0.00041348478,0.00023237623,0.0006596564,0.0005080376,0.0004626199],"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":[0.00089102506,0.00030252928,0.5193793,0.0002647936,0.00014476679,0.34592164,0.0012292593,0.00047102978,0.08188657,0.0005370069,0.0016932106,0.047278766],"study_design_scores_gemma":[0.000055266602,0.00055315037,0.39252114,0.000063897656,0.000115144074,0.59903127,0.0002867411,0.0005719641,0.0046934923,0.00033867813,0.001748635,0.000020640062],"about_ca_topic_score_codex":0.00061362475,"about_ca_topic_score_gemma":0.00091443205,"teacher_disagreement_score":0.0026176288,"about_ca_system_score_codex":0.0001553533,"about_ca_system_score_gemma":0.00018186962,"threshold_uncertainty_score":0.008756816},"labels":[],"label_agreement":null},{"id":"W4406132855","doi":"10.1097/pxr.0000000000000426","title":"Foot orthosis design for children with Charcot-Marie-Tooth and impact on gait","year":2025,"lang":"en","type":"article","venue":"Prosthetics and Orthotics International","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":0,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Université de Montréal; Quebec Rehabilitation Research Network; Université du Québec à Montréal; Centre Hospitalier Universitaire Sainte-Justine","funders":"Centre hospitalier universitaire Sainte-Justine","keywords":"Gait; Physical medicine and rehabilitation; Medicine; Range of motion; Tooth disease; Foot deformity; Foot (prosody); Deformity; Plantar pressure; Gait analysis; Preferred walking speed; Physical therapy; Orthotics; Foot Orthoses; Gait cycle; Orthodontics; Disease; Surgery","score_opus":0.02705902905782913,"score_gpt":0.2858043652776236,"score_spread":0.25874533621979445,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4406132855","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":[0.994365,0.0003251519,0.004391014,0.000033788026,0.000028089533,0.00026977228,0.0001338913,0.000020385758,0.00043289154],"genre_scores_gemma":[0.96553504,0.0003372636,0.032682195,0.000023056093,0.000023449074,0.0007216455,0.00027068277,0.0000128333095,0.0003937857],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99941754,0.00021679244,0.00007734308,0.00007410794,0.00015971663,0.00005445036],"domain_scores_gemma":[0.999408,0.00019852599,0.00019739891,0.00004018411,0.00008370808,0.000072149654],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0010518974,0.0006154933,0.0003887309,0.00070514646,0.00020088116,0.00023062479,0.00029927888,0.00028062242,0.0014272184],"category_scores_gemma":[0.0016633279,0.00014203583,0.00060143165,0.00033401386,0.00019089798,0.00018030098,0.00031038732,0.0002114196,0.00015064036],"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":[0.01912046,0.008400385,0.4393349,0.0021919752,0.00028702294,0.0026230768,0.0008382861,0.005027269,0.08503523,0.000765085,0.0011436255,0.4352326],"study_design_scores_gemma":[0.0015252971,0.08766984,0.8633107,0.00037846665,0.0004634533,0.008112044,0.0013169998,0.006762526,0.02198013,0.00059085304,0.0078014815,0.00008817628],"about_ca_topic_score_codex":0.00049111596,"about_ca_topic_score_gemma":0.0012623636,"teacher_disagreement_score":0.0014272184,"about_ca_system_score_codex":0.00025411256,"about_ca_system_score_gemma":0.0003147751,"threshold_uncertainty_score":0.0055630803},"labels":[],"label_agreement":null},{"id":"W4406207072","doi":"10.2139/ssrn.5087374","title":"Genetic Risk of Axonal Neuropathy Following Infection","year":2025,"lang":"en","type":"preprint","venue":"SSRN Electronic Journal","topic":"Hereditary Neurological Disorders","field":"Neuroscience","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":"University of Ottawa","funders":"","keywords":"Medicine; Neuroscience; Genetics; Biology","score_opus":0.014626569443717742,"score_gpt":0.2565313897987212,"score_spread":0.24190482035500346,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4406207072","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":[0.995606,0.00025970157,0.00038493538,0.00022327591,0.000028200922,0.000007365776,0.00054781674,0.00001805117,0.0029245003],"genre_scores_gemma":[0.9982316,0.00018469978,0.00018619241,0.000025225887,0.000040968855,0.0000042502284,0.00025017228,0.000010079827,0.0010667803],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9995814,0.0001279661,0.00003815528,0.000100712314,0.000066704684,0.00008507966],"domain_scores_gemma":[0.99827015,0.00067312026,0.0005464711,0.00016556088,0.00010622151,0.00023846998],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00035873507,0.0005122318,0.00041527004,0.0010275268,0.00048475087,0.00069938647,0.00041090787,0.0011663368,0.0128225535],"category_scores_gemma":[0.00328098,0.00025399626,0.00040697094,0.0010775318,0.0003781237,0.00037306742,0.0005743461,0.00061026885,0.0009186924],"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":[0.0032111555,0.00038000089,0.9530996,0.00011828574,0.00052754773,0.012470497,0.00044870694,0.0007263758,0.008775843,0.0018734193,0.0017180275,0.016650654],"study_design_scores_gemma":[0.000055650537,0.00041558815,0.97703576,0.0000672622,0.0002741753,0.015802633,0.00030632358,0.0012223566,0.0011882865,0.0029026829,0.0006996547,0.000029697812],"about_ca_topic_score_codex":0.0016614335,"about_ca_topic_score_gemma":0.00066075224,"teacher_disagreement_score":0.0128225535,"about_ca_system_score_codex":0.00018418544,"about_ca_system_score_gemma":0.00021652672,"threshold_uncertainty_score":0.042895675},"labels":[],"label_agreement":null},{"id":"W4406413703","doi":"10.1016/s1762-0953(21)30700-2","title":"10.1016/s1762-0953(21)30700-2","year":2000,"lang":"en","type":"article","venue":"Time to knit","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":0,"is_retracted":false,"has_abstract":false,"route_ca_aff":false,"route_ca_fund":false,"route_ca_venue":true,"route_about_ca":false,"ca_institutions":"","funders":"","keywords":"Medicine; Gynecology","score_opus":0.01456539839540875,"score_gpt":0.18987182056070992,"score_spread":0.17530642216530118,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4406413703","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":[0.00037389577,0.0004826793,0.00062763126,0.00038807458,0.00036860278,0.000116302464,0.00079077337,0.00086606183,0.9959859],"genre_scores_gemma":[0.00045750616,0.00021171641,0.0003867879,0.00022544726,0.000088236506,0.0000645682,0.00038834653,0.00014808433,0.9980293],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.99928313,0.000045656187,0.00006872925,0.00025797947,0.00018254778,0.00016200622],"domain_scores_gemma":[0.9975074,0.000645557,0.00014331756,0.0002674309,0.0004599179,0.00097643584],"candidate_categories":["insufficient_payload"],"consensus_categories":["insufficient_payload"],"category_scores_codex":[0.0011803017,0.0031062549,0.0021363432,0.003053598,0.0028128002,0.003657203,0.0037723694,0.0064072926,0.99149674],"category_scores_gemma":[0.0017816214,0.0011233981,0.001848345,0.0022504816,0.0020188312,0.0056516784,0.003833197,0.0031205823,0.9932708],"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":[0.0004495642,0.00022714498,0.0007499882,0.00080476794,0.00004287209,0.00031484105,0.000108398286,0.00043027225,0.002001388,0.0053227562,0.39384854,0.5956994],"study_design_scores_gemma":[0.000077558,0.00012131642,0.00074152777,0.0003531688,0.000015735028,0.00043634343,0.000113207534,0.00019758097,0.00037627856,0.00065156654,0.996887,0.000028697912],"about_ca_topic_score_codex":0.004115142,"about_ca_topic_score_gemma":0.0037142881,"teacher_disagreement_score":0.008503258,"about_ca_system_score_codex":0.0012088484,"about_ca_system_score_gemma":0.0012167303,"threshold_uncertainty_score":0.01212889},"labels":[],"label_agreement":null},{"id":"W4406443554","doi":"10.1016/s0246-0378(22)44911-6","title":"10.1016/s0246-0378(22)44911-6","year":2000,"lang":"en","type":"article","venue":"Time to knit","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":0,"is_retracted":false,"has_abstract":false,"route_ca_aff":false,"route_ca_fund":false,"route_ca_venue":true,"route_about_ca":false,"ca_institutions":"","funders":"","keywords":"Philosophy","score_opus":0.01513305714163415,"score_gpt":0.19627058859484514,"score_spread":0.181137531453211,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4406443554","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":[0.00035825375,0.00051684317,0.0005598041,0.0004490771,0.00041163518,0.00010209676,0.0007091717,0.0007624067,0.9961308],"genre_scores_gemma":[0.00045223738,0.00019168486,0.00025254334,0.0001650609,0.00007813167,0.000039387687,0.00027711125,0.00011598897,0.99842787],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.99939775,0.000035277582,0.000056163542,0.00020104769,0.00016947051,0.00014039714],"domain_scores_gemma":[0.9976119,0.00058210676,0.00015453684,0.00025318612,0.0005297631,0.0008685423],"candidate_categories":["insufficient_payload"],"consensus_categories":["insufficient_payload"],"category_scores_codex":[0.0010756693,0.0024081601,0.0017255291,0.0024069815,0.0021943527,0.0035259605,0.0029390207,0.005388461,0.98901373],"category_scores_gemma":[0.0016485921,0.00085885765,0.0015441763,0.0019886305,0.0016964864,0.004361672,0.0029617315,0.0025923501,0.99143094],"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":[0.00036232895,0.00018278424,0.000618906,0.00065032847,0.000035420897,0.00025049623,0.00009197246,0.0003503533,0.0019309942,0.005484427,0.36627883,0.6237632],"study_design_scores_gemma":[0.00004853552,0.00008318218,0.0006330959,0.00024842066,0.000011469276,0.00029661972,0.00008091171,0.00013540215,0.00033883806,0.00052545767,0.9975793,0.000018850185],"about_ca_topic_score_codex":0.0040851026,"about_ca_topic_score_gemma":0.0033631537,"teacher_disagreement_score":0.0109862685,"about_ca_system_score_codex":0.0010828173,"about_ca_system_score_gemma":0.0011655905,"threshold_uncertainty_score":0.015670598},"labels":[],"label_agreement":null},{"id":"W4406452173","doi":"10.1016/s1155-1917(99)00008-2","title":"10.1016/s1155-1917(99)00008-2","year":2000,"lang":"en","type":"article","venue":"Time to knit","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":4,"is_retracted":false,"has_abstract":false,"route_ca_aff":false,"route_ca_fund":false,"route_ca_venue":true,"route_about_ca":false,"ca_institutions":"","funders":"","keywords":"Medicine; General surgery; Surgery","score_opus":0.015513150219725236,"score_gpt":0.1943988573541189,"score_spread":0.17888570713439367,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4406452173","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":[0.00037172483,0.00043489758,0.0005657334,0.00041090776,0.0003311664,0.00009454845,0.00059036067,0.0007616406,0.99643904],"genre_scores_gemma":[0.00053651625,0.00018469253,0.0003380854,0.00020899506,0.0000777737,0.000051250932,0.00032129895,0.00013168776,0.99814963],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.99934787,0.00004002122,0.00005971528,0.00020656906,0.00018970671,0.00015621287],"domain_scores_gemma":[0.99800795,0.00046606787,0.00012222261,0.00023757642,0.0004201,0.0007461112],"candidate_categories":["insufficient_payload"],"consensus_categories":["insufficient_payload"],"category_scores_codex":[0.0009942922,0.0025465605,0.001729304,0.0028091671,0.002493865,0.0033816309,0.0030428013,0.0057168277,0.98957574],"category_scores_gemma":[0.0015859508,0.00090000883,0.0016646057,0.0017323211,0.0017952473,0.004583979,0.0035042008,0.0026854516,0.9926825],"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":[0.00039091986,0.00022138217,0.0008638406,0.0006271738,0.00004344542,0.00031117976,0.00009890041,0.00041518678,0.0018636063,0.0046492666,0.38899818,0.601517],"study_design_scores_gemma":[0.00006466732,0.00010683498,0.00091370876,0.00034595674,0.000016668953,0.00049206463,0.00010682632,0.00020049086,0.00041092845,0.00075117603,0.99656516,0.00002551324],"about_ca_topic_score_codex":0.0042149075,"about_ca_topic_score_gemma":0.0035839565,"teacher_disagreement_score":0.010424256,"about_ca_system_score_codex":0.0011215749,"about_ca_system_score_gemma":0.0010240893,"threshold_uncertainty_score":0.0148688555},"labels":[],"label_agreement":null},{"id":"W4406502446","doi":"10.1016/s0246-0378(19)30366-5","title":"10.1016/s0246-0378(19)30366-5","year":2000,"lang":"en","type":"article","venue":"Time to knit","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":0,"is_retracted":false,"has_abstract":false,"route_ca_aff":false,"route_ca_fund":false,"route_ca_venue":true,"route_about_ca":false,"ca_institutions":"","funders":"","keywords":"Psychology","score_opus":0.018006407189553045,"score_gpt":0.2024575501981024,"score_spread":0.18445114300854937,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4406502446","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":[0.0004044427,0.000489879,0.00053913734,0.0004145905,0.00039952688,0.00011478415,0.0006987203,0.0007052556,0.99623364],"genre_scores_gemma":[0.00046045287,0.00017689037,0.00024025084,0.00017096622,0.00007219983,0.000045179866,0.00026100056,0.00010432095,0.9984687],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.99934965,0.000038948252,0.000058328016,0.00023722021,0.00016217514,0.00015360278],"domain_scores_gemma":[0.99771357,0.0005523062,0.00014090343,0.00023497404,0.00045936895,0.0008988717],"candidate_categories":["insufficient_payload"],"consensus_categories":["insufficient_payload"],"category_scores_codex":[0.0011324072,0.0026099377,0.0018627429,0.002465011,0.002583761,0.0036550106,0.003220154,0.0059629595,0.9901267],"category_scores_gemma":[0.0015557522,0.0009664854,0.0015855462,0.0020666362,0.0020449425,0.0046290965,0.003346566,0.0026759275,0.9914854],"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":[0.00047637807,0.0002124808,0.0006935405,0.000725156,0.00003925126,0.00031512382,0.00011828903,0.0003952182,0.002148843,0.0060510836,0.36481664,0.62400806],"study_design_scores_gemma":[0.000058368812,0.0001074257,0.0006474653,0.00027662513,0.000012129372,0.00032712176,0.000099269855,0.00015424665,0.00033266,0.0005446843,0.99741983,0.000020121306],"about_ca_topic_score_codex":0.003969088,"about_ca_topic_score_gemma":0.0035437848,"teacher_disagreement_score":0.009873271,"about_ca_system_score_codex":0.0011393413,"about_ca_system_score_gemma":0.0011448953,"threshold_uncertainty_score":0.014082909},"labels":[],"label_agreement":null},{"id":"W4406507455","doi":"10.1016/s0246-0378(16)65743-3","title":"10.1016/s0246-0378(16)65743-3","year":2000,"lang":"en","type":"article","venue":"Time to knit","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":0,"is_retracted":false,"has_abstract":false,"route_ca_aff":false,"route_ca_fund":false,"route_ca_venue":true,"route_about_ca":false,"ca_institutions":"","funders":"","keywords":"Medicine; Cardiology","score_opus":0.01581665692345899,"score_gpt":0.19553856280596177,"score_spread":0.17972190588250278,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4406507455","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":[0.0003324478,0.00050539215,0.00054748164,0.00042359755,0.00037361163,0.000097850454,0.0007242626,0.000734503,0.9962608],"genre_scores_gemma":[0.0004471499,0.00018921641,0.00024536467,0.0001593523,0.00007085696,0.00003955875,0.00027138012,0.00011396772,0.9984633],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.9994549,0.000032111384,0.000049912887,0.00019307481,0.00014629558,0.00012361254],"domain_scores_gemma":[0.99787045,0.0005150605,0.00014683839,0.00022391503,0.0004481161,0.0007956425],"candidate_categories":["insufficient_payload"],"consensus_categories":["insufficient_payload"],"category_scores_codex":[0.001028181,0.0023944757,0.0017359722,0.0023310436,0.002264641,0.0035409806,0.0029522534,0.005293952,0.9889404],"category_scores_gemma":[0.001603848,0.0008536205,0.0015025609,0.0020305156,0.001749836,0.004295662,0.0030017747,0.0025458655,0.99166054],"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":[0.00037776516,0.00016573364,0.0006021479,0.0006470518,0.000034103854,0.0002464654,0.00009763591,0.00038159496,0.0018774417,0.0056770006,0.38381773,0.60607517],"study_design_scores_gemma":[0.000048480484,0.00008054012,0.0005615956,0.00024453996,0.000010785041,0.00027995632,0.00008398907,0.00013531724,0.0002965106,0.00053921377,0.99770135,0.00001781607],"about_ca_topic_score_codex":0.0043017524,"about_ca_topic_score_gemma":0.0036130631,"teacher_disagreement_score":0.011059582,"about_ca_system_score_codex":0.0011261808,"about_ca_system_score_gemma":0.0011503575,"threshold_uncertainty_score":0.015775144},"labels":[],"label_agreement":null},{"id":"W4406535929","doi":"10.1016/s1283-0828(20)30191-5","title":"10.1016/s1283-0828(20)30191-5","year":2000,"lang":"en","type":"article","venue":"Time to knit","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":0,"is_retracted":false,"has_abstract":false,"route_ca_aff":false,"route_ca_fund":false,"route_ca_venue":true,"route_about_ca":false,"ca_institutions":"","funders":"","keywords":"Computer science","score_opus":0.015288767855068743,"score_gpt":0.194704125232915,"score_spread":0.17941535737784625,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4406535929","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":[0.00038991464,0.00049913325,0.0007072801,0.00039768196,0.00034377814,0.00011745696,0.0007538111,0.00092051143,0.99587053],"genre_scores_gemma":[0.00056268583,0.00023176639,0.0003932564,0.00023040139,0.00010385024,0.0000667444,0.00041052164,0.00015663283,0.9978442],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.9993192,0.0000416158,0.00006190797,0.00023926758,0.00017788558,0.00016018553],"domain_scores_gemma":[0.99755186,0.0006372213,0.0001406886,0.0002651678,0.00040899788,0.0009961152],"candidate_categories":["insufficient_payload"],"consensus_categories":["insufficient_payload"],"category_scores_codex":[0.0011138333,0.0029249263,0.0020346553,0.002792257,0.002503843,0.0036710873,0.003762571,0.0065407553,0.9901462],"category_scores_gemma":[0.0016625031,0.0010389918,0.0017593665,0.0019205211,0.0018748413,0.0050887205,0.0036633448,0.0029118846,0.99276674],"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":[0.00049652427,0.00024501298,0.0006797097,0.0007134841,0.000042251195,0.00030187695,0.0000975267,0.00042636076,0.0019027333,0.0051817927,0.37645447,0.6134583],"study_design_scores_gemma":[0.00009522659,0.00014382791,0.0008297779,0.00034596972,0.00001757895,0.0004588149,0.000108573426,0.00023206061,0.0004097424,0.0007793626,0.9965502,0.000028777544],"about_ca_topic_score_codex":0.0038056653,"about_ca_topic_score_gemma":0.0032114172,"teacher_disagreement_score":0.00985378,"about_ca_system_score_codex":0.001081605,"about_ca_system_score_gemma":0.0010847207,"threshold_uncertainty_score":0.0140551925},"labels":[],"label_agreement":null},{"id":"W4406540639","doi":"10.1016/s0246-0378(19)30361-6","title":"10.1016/s0246-0378(19)30361-6","year":2000,"lang":"en","type":"article","venue":"Time to knit","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":0,"is_retracted":false,"has_abstract":false,"route_ca_aff":false,"route_ca_fund":false,"route_ca_venue":true,"route_about_ca":false,"ca_institutions":"","funders":"","keywords":"Computer science","score_opus":0.01800727000679215,"score_gpt":0.2024441282275989,"score_spread":0.18443685822080677,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4406540639","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":[0.00041911576,0.00052794226,0.00058545347,0.00044148957,0.00040455465,0.000120719145,0.00075419655,0.0007662959,0.99598026],"genre_scores_gemma":[0.00047883365,0.00018278262,0.0002601549,0.00017383303,0.00007445044,0.00004714327,0.00028355644,0.00011241082,0.99838686],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.99934536,0.000037815502,0.000058577167,0.00023828192,0.00016432369,0.00015562467],"domain_scores_gemma":[0.9976822,0.0005550472,0.00014962433,0.00024334488,0.0004507328,0.0009190534],"candidate_categories":["insufficient_payload"],"consensus_categories":["insufficient_payload"],"category_scores_codex":[0.0011621242,0.002639238,0.0019237971,0.0024798787,0.0026248854,0.0036855603,0.003328837,0.0061195786,0.9901861],"category_scores_gemma":[0.0015937255,0.0010045302,0.0016139592,0.002027646,0.0021231086,0.0047416924,0.0034335179,0.0027293519,0.9918086],"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":[0.0004902148,0.00021654459,0.00068790634,0.0007597278,0.00004035705,0.00031592487,0.00012125008,0.00038469033,0.0022494325,0.006275392,0.35587135,0.63258725],"study_design_scores_gemma":[0.00006201811,0.0001083558,0.0006462657,0.00027094106,0.000012507868,0.0003431329,0.00010122648,0.00015333344,0.00035600233,0.00057759206,0.99734807,0.00002054598],"about_ca_topic_score_codex":0.003974506,"about_ca_topic_score_gemma":0.0034580082,"teacher_disagreement_score":0.009813905,"about_ca_system_score_codex":0.0011354019,"about_ca_system_score_gemma":0.0011626148,"threshold_uncertainty_score":0.01399827},"labels":[],"label_agreement":null},{"id":"W4406541019","doi":"10.1016/s0246-0378(14)58201-2","title":"10.1016/s0246-0378(14)58201-2","year":2000,"lang":"en","type":"article","venue":"Time to knit","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":0,"is_retracted":false,"has_abstract":false,"route_ca_aff":false,"route_ca_fund":false,"route_ca_venue":true,"route_about_ca":false,"ca_institutions":"","funders":"","keywords":"Biology","score_opus":0.015852135908817268,"score_gpt":0.1961778758414864,"score_spread":0.18032573993266915,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4406541019","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":[0.00036499248,0.00039768688,0.0005325893,0.00040513786,0.00035236197,0.00010868941,0.0006710666,0.00073929207,0.9964282],"genre_scores_gemma":[0.0004586516,0.00015415777,0.0002509485,0.00015490258,0.000067074376,0.00004118315,0.00024715616,0.00011570684,0.99851006],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.9993825,0.000038999337,0.000055107925,0.00021948147,0.00016458497,0.000139259],"domain_scores_gemma":[0.9977385,0.0005897619,0.00013461344,0.00023466772,0.00049123116,0.00081120303],"candidate_categories":["insufficient_payload"],"consensus_categories":["insufficient_payload"],"category_scores_codex":[0.0011024583,0.0024868113,0.0017031782,0.0026076909,0.002393625,0.0034073163,0.0029404927,0.0054692123,0.98966926],"category_scores_gemma":[0.0016148761,0.00086408487,0.0015326178,0.0020696968,0.0018591771,0.0042206636,0.0031854,0.0024856392,0.99131507],"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":[0.00040258726,0.00019309975,0.0006648059,0.0006232427,0.000033096145,0.0002794351,0.00009964049,0.00040033337,0.0019975498,0.0055526504,0.38364735,0.6061061],"study_design_scores_gemma":[0.000051620675,0.0000926378,0.0006491176,0.0002471607,0.000010414043,0.00028352195,0.00009076817,0.00016397948,0.0003400737,0.00053279387,0.9975193,0.000018461506],"about_ca_topic_score_codex":0.004354827,"about_ca_topic_score_gemma":0.0036954102,"teacher_disagreement_score":0.010330737,"about_ca_system_score_codex":0.0011573916,"about_ca_system_score_gemma":0.0010997357,"threshold_uncertainty_score":0.01473552},"labels":[],"label_agreement":null},{"id":"W4406554938","doi":"10.1016/s1634-6939(15)73093-0","title":"10.1016/s1634-6939(15)73093-0","year":2000,"lang":"en","type":"article","venue":"Time to knit","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":0,"is_retracted":false,"has_abstract":false,"route_ca_aff":false,"route_ca_fund":false,"route_ca_venue":true,"route_about_ca":false,"ca_institutions":"","funders":"","keywords":"Computer science","score_opus":0.01440657537528532,"score_gpt":0.1888870544053929,"score_spread":0.1744804790301076,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4406554938","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":[0.00030171408,0.00035972375,0.00049145997,0.00035796576,0.0003319431,0.00008716871,0.0006011473,0.00074994395,0.9967188],"genre_scores_gemma":[0.00041680364,0.00018157602,0.00029211317,0.00019572405,0.00008604285,0.000046642057,0.00031303562,0.00013814577,0.99832994],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.99941707,0.000036403944,0.000052835454,0.00018578685,0.0001722796,0.00013565367],"domain_scores_gemma":[0.9975744,0.0005656048,0.00013231917,0.00026941134,0.0004630282,0.000995202],"candidate_categories":["insufficient_payload"],"consensus_categories":["insufficient_payload"],"category_scores_codex":[0.0010195655,0.0025665164,0.0016926948,0.0028857943,0.002519209,0.0034479205,0.0030940187,0.0059180553,0.99021673],"category_scores_gemma":[0.0017714057,0.00096120924,0.0016467755,0.0019128752,0.0017008771,0.0048039523,0.0037351043,0.0027749913,0.9923878],"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":[0.0003251576,0.00020719359,0.00066588144,0.00050635514,0.000031926695,0.00023325757,0.00008258251,0.00038204802,0.001489469,0.0042454596,0.43863475,0.55319595],"study_design_scores_gemma":[0.000061105486,0.00009019994,0.0007979057,0.00027886374,0.000011333385,0.00033361235,0.000092394635,0.0001639474,0.00029346356,0.000598079,0.99725586,0.000023170827],"about_ca_topic_score_codex":0.005122533,"about_ca_topic_score_gemma":0.0045593954,"teacher_disagreement_score":0.009783268,"about_ca_system_score_codex":0.001149543,"about_ca_system_score_gemma":0.0012609703,"threshold_uncertainty_score":0.01395458},"labels":[],"label_agreement":null},{"id":"W4406576706","doi":"10.1016/s1553-3212(05)71079-7","title":"10.1016/s1553-3212(05)71079-7","year":2000,"lang":"en","type":"article","venue":"Time to knit","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":0,"is_retracted":false,"has_abstract":false,"route_ca_aff":false,"route_ca_fund":false,"route_ca_venue":true,"route_about_ca":false,"ca_institutions":"","funders":"","keywords":"Triad (sociology); Polyneuropathy; Medicine; Anatomy; Physical medicine and rehabilitation; Psychology; Surgery; Psychoanalysis","score_opus":0.01530608190725136,"score_gpt":0.19120275809842868,"score_spread":0.17589667619117733,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4406576706","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":[0.00040805564,0.0005125819,0.0005919558,0.0004955936,0.00036987872,0.000101707534,0.0007346848,0.0008572809,0.99592835],"genre_scores_gemma":[0.0004921837,0.00019937122,0.00028288277,0.000222361,0.000079565296,0.00005111358,0.00033900168,0.0001286474,0.9982048],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.9993672,0.000042739317,0.00006247524,0.0002091307,0.0001682346,0.00015034903],"domain_scores_gemma":[0.9974401,0.0006459359,0.00017171283,0.00027383323,0.0005018354,0.0009665053],"candidate_categories":["insufficient_payload"],"consensus_categories":["insufficient_payload"],"category_scores_codex":[0.0012045531,0.0026529965,0.0019636876,0.0026829804,0.002691187,0.0038514081,0.003339807,0.0068313177,0.9895392],"category_scores_gemma":[0.0017636325,0.00096574344,0.0015806066,0.001912003,0.0018738508,0.005349357,0.0035118822,0.0029232095,0.9930529],"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":[0.00042575086,0.0002255503,0.00074316066,0.0006474666,0.000037650967,0.00027973021,0.00010093917,0.00044277505,0.0019049293,0.0052878885,0.40553242,0.58437175],"study_design_scores_gemma":[0.00007005257,0.0001116753,0.00079295103,0.0003316203,0.000014247115,0.0003672323,0.00011336547,0.0001983238,0.00038722137,0.0007401358,0.996847,0.000026093683],"about_ca_topic_score_codex":0.00414908,"about_ca_topic_score_gemma":0.003355658,"teacher_disagreement_score":0.010460794,"about_ca_system_score_codex":0.0011779806,"about_ca_system_score_gemma":0.0013086486,"threshold_uncertainty_score":0.014921069},"labels":[],"label_agreement":null},{"id":"W4406641094","doi":"10.1016/b978-2-294-02147-3.50010-4","title":"10.1016/b978-2-294-02147-3.50010-4","year":2000,"lang":"en","type":"book-chapter","venue":"Time to knit","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":0,"is_retracted":false,"has_abstract":false,"route_ca_aff":false,"route_ca_fund":false,"route_ca_venue":true,"route_about_ca":false,"ca_institutions":"","funders":"","keywords":"Medicine","score_opus":0.020733468090743598,"score_gpt":0.19167887072172854,"score_spread":0.17094540263098496,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4406641094","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":[0.00015984762,0.00051278004,0.00076820055,0.0002512287,0.00015273041,0.000033558517,0.0005201406,0.000767007,0.9968346],"genre_scores_gemma":[0.0004103475,0.00025946993,0.0002974798,0.000098544464,0.000032404296,0.000023292685,0.00027554398,0.00017649887,0.99842644],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.99965346,0.000019518455,0.000022375501,0.000121040095,0.000119506214,0.000064063526],"domain_scores_gemma":[0.9987546,0.00043129796,0.00008398565,0.00015434383,0.00020990937,0.00036586457],"candidate_categories":["insufficient_payload"],"consensus_categories":["insufficient_payload"],"category_scores_codex":[0.00066801475,0.0019590473,0.0012584919,0.001597681,0.0012222356,0.004050187,0.0023228684,0.003651385,0.978218],"category_scores_gemma":[0.0013375533,0.00073020614,0.0007728854,0.0016765002,0.0010643642,0.004012587,0.0028808385,0.0020254385,0.98795265],"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":[0.00012936995,0.000089996065,0.00027747132,0.00043380333,0.000014661499,0.00013293263,0.00008577294,0.0003270657,0.0019179367,0.0072814967,0.4023413,0.5869682],"study_design_scores_gemma":[0.000014293497,0.000033707187,0.00037791088,0.00022707079,0.0000061798983,0.00019036199,0.00006099178,0.000104264116,0.00028502417,0.0012338022,0.99745566,0.00001083009],"about_ca_topic_score_codex":0.0025601415,"about_ca_topic_score_gemma":0.0027694167,"teacher_disagreement_score":0.021781981,"about_ca_system_score_codex":0.0008257349,"about_ca_system_score_gemma":0.00069011026,"threshold_uncertainty_score":0.031069338},"labels":[],"label_agreement":null},{"id":"W4406645752","doi":"10.1016/b978-84-8086-708-5.00013-1","title":"10.1016/b978-84-8086-708-5.00013-1","year":2000,"lang":"en","type":"book-chapter","venue":"Time to knit","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":0,"is_retracted":false,"has_abstract":false,"route_ca_aff":false,"route_ca_fund":false,"route_ca_venue":true,"route_about_ca":false,"ca_institutions":"","funders":"","keywords":"Computer science","score_opus":0.020867263518571186,"score_gpt":0.19055272228494316,"score_spread":0.16968545876637198,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4406645752","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":[0.00013669832,0.0005859062,0.00059045816,0.00020890032,0.00015996062,0.0000321708,0.00038829807,0.00051432644,0.9973833],"genre_scores_gemma":[0.0003503199,0.0003426575,0.0002641045,0.000092630136,0.000034746437,0.00002358306,0.00023939264,0.00012985709,0.9985227],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.9996927,0.000016383623,0.000018598854,0.000106887834,0.000105565814,0.000059905087],"domain_scores_gemma":[0.99892527,0.0003602293,0.0000697493,0.000118600394,0.00018674019,0.00033942115],"candidate_categories":["insufficient_payload"],"consensus_categories":["insufficient_payload"],"category_scores_codex":[0.0006020841,0.0021091145,0.001253637,0.0016894853,0.001240413,0.0036716089,0.002251841,0.0034410395,0.97432864],"category_scores_gemma":[0.0011071945,0.0007110416,0.00076074165,0.0017277687,0.0010788837,0.0039522937,0.0027416197,0.002008383,0.985254],"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":[0.000115426265,0.00009861019,0.0002538309,0.00043595,0.00001370613,0.0001312379,0.00008891933,0.00027967276,0.001956063,0.0066213445,0.41889456,0.57111067],"study_design_scores_gemma":[0.000013330149,0.000035885056,0.0004373012,0.00025769812,0.000006106818,0.00019810288,0.00006652806,0.000088963694,0.0002382634,0.0011818619,0.9974654,0.000010577973],"about_ca_topic_score_codex":0.0031267055,"about_ca_topic_score_gemma":0.0033784679,"teacher_disagreement_score":0.025671363,"about_ca_system_score_codex":0.0007555457,"about_ca_system_score_gemma":0.00069165556,"threshold_uncertainty_score":0.03661698},"labels":[],"label_agreement":null},{"id":"W4406648132","doi":"10.1016/b978-3-437-21073-0.00033-7","title":"10.1016/b978-3-437-21073-0.00033-7","year":2000,"lang":"en","type":"book-chapter","venue":"Time to knit","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":0,"is_retracted":false,"has_abstract":false,"route_ca_aff":false,"route_ca_fund":false,"route_ca_venue":true,"route_about_ca":false,"ca_institutions":"","funders":"","keywords":"Computer science","score_opus":0.021079962648836416,"score_gpt":0.19095452794832415,"score_spread":0.16987456529948775,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4406648132","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":[0.00014411643,0.0005234494,0.00070755655,0.00020498142,0.0001441633,0.00003618413,0.0004724227,0.00072790415,0.9970392],"genre_scores_gemma":[0.00040408914,0.0003059187,0.00033553672,0.00010083175,0.000036306978,0.000028571201,0.00032937716,0.00018152659,0.9982779],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.99966264,0.000018374396,0.00002071085,0.00011329777,0.0001181736,0.00006675439],"domain_scores_gemma":[0.9988439,0.00039456648,0.00007761492,0.00014605549,0.00018562809,0.00035216514],"candidate_categories":["insufficient_payload"],"consensus_categories":["insufficient_payload"],"category_scores_codex":[0.00067235314,0.0021751823,0.0013247959,0.0016953311,0.0012379297,0.003800475,0.0024943394,0.0035560047,0.9764583],"category_scores_gemma":[0.0012120075,0.0007359715,0.0008306531,0.0016665309,0.0011176096,0.003761595,0.003218411,0.001940736,0.9875243],"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":[0.0001323275,0.00010336988,0.000273194,0.00044480737,0.000016770467,0.00013790348,0.00008442349,0.0003289963,0.002175067,0.007486754,0.37835735,0.6104591],"study_design_scores_gemma":[0.000016444905,0.00003896849,0.0004425352,0.00025126603,0.000006770914,0.0001971187,0.000060500686,0.000097119235,0.0002861222,0.0013268829,0.9972644,0.000011930516],"about_ca_topic_score_codex":0.0029333308,"about_ca_topic_score_gemma":0.0030171159,"teacher_disagreement_score":0.023541689,"about_ca_system_score_codex":0.00077046757,"about_ca_system_score_gemma":0.0007224105,"threshold_uncertainty_score":0.03357929},"labels":[],"label_agreement":null},{"id":"W4406648234","doi":"10.1016/b978-3-437-21073-0.00005-2","title":"10.1016/b978-3-437-21073-0.00005-2","year":2000,"lang":"en","type":"book-chapter","venue":"Time to knit","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":0,"is_retracted":false,"has_abstract":false,"route_ca_aff":false,"route_ca_fund":false,"route_ca_venue":true,"route_about_ca":false,"ca_institutions":"","funders":"","keywords":"Medicine","score_opus":0.02111309844710342,"score_gpt":0.19139187402334187,"score_spread":0.17027877557623844,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4406648234","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":[0.00012558291,0.00042908106,0.0005921934,0.00019767236,0.0001361889,0.00003114665,0.00039658826,0.0005751362,0.9975165],"genre_scores_gemma":[0.00039717948,0.00025056937,0.000319463,0.000094739335,0.000033216726,0.000023544573,0.00027013262,0.0001661204,0.998445],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.9996903,0.000016345411,0.000018486517,0.00010207799,0.00011365663,0.000059084796],"domain_scores_gemma":[0.99901676,0.0003048251,0.00006435806,0.00012120931,0.00017648841,0.00031641376],"candidate_categories":["insufficient_payload"],"consensus_categories":["insufficient_payload"],"category_scores_codex":[0.0005912503,0.0017987774,0.0010580216,0.0014971651,0.0011194055,0.0035258704,0.0021147332,0.003143087,0.97575605],"category_scores_gemma":[0.0011723321,0.000631146,0.0007106067,0.0014019021,0.0009904277,0.0033110816,0.0028258236,0.0017035615,0.98616344],"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":[0.00011531639,0.00008810009,0.00026993602,0.00036971623,0.000012882723,0.00012217264,0.00007346977,0.00027411303,0.0018247063,0.0074757715,0.38393924,0.6054345],"study_design_scores_gemma":[0.000012928364,0.000029004028,0.0003884486,0.00019497109,0.000005018633,0.00017440067,0.000046020003,0.00007871536,0.00021921085,0.0011169629,0.99772483,0.000009452534],"about_ca_topic_score_codex":0.0027642366,"about_ca_topic_score_gemma":0.0029830558,"teacher_disagreement_score":0.02424395,"about_ca_system_score_codex":0.00075299613,"about_ca_system_score_gemma":0.00065872254,"threshold_uncertainty_score":0.034580946},"labels":[],"label_agreement":null},{"id":"W4406652408","doi":"10.1016/b978-1-4160-2467-5.50056-7","title":"10.1016/b978-1-4160-2467-5.50056-7","year":2000,"lang":"en","type":"book-chapter","venue":"Time to knit","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":0,"is_retracted":false,"has_abstract":false,"route_ca_aff":false,"route_ca_fund":false,"route_ca_venue":true,"route_about_ca":false,"ca_institutions":"","funders":"","keywords":"Psychology","score_opus":0.021034494095316165,"score_gpt":0.19099009060783617,"score_spread":0.16995559651252,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4406652408","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":[0.00015239537,0.00065361505,0.0007368009,0.00024328221,0.0001529132,0.000034997556,0.0005143983,0.0007384924,0.99677294],"genre_scores_gemma":[0.00037450832,0.00033900994,0.00031635445,0.000099481476,0.000031981544,0.000025031628,0.00030783453,0.00016469214,0.99834096],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.9996798,0.00001811781,0.000020139874,0.00010610909,0.00011377407,0.00006204578],"domain_scores_gemma":[0.99884343,0.00038787833,0.00007827952,0.00014737583,0.00018611582,0.0003569767],"candidate_categories":["insufficient_payload"],"consensus_categories":["insufficient_payload"],"category_scores_codex":[0.00064531394,0.002013175,0.0012374853,0.0016206221,0.0011589791,0.003777046,0.0023887565,0.003534591,0.97434855],"category_scores_gemma":[0.0011805074,0.0006932096,0.0007711896,0.0015732986,0.0010046609,0.0038453739,0.0031880597,0.0019559546,0.98594207],"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":[0.000119152246,0.00009475993,0.00024340818,0.00043334925,0.000013628243,0.00012765749,0.000076716104,0.00028145997,0.0020387773,0.006895918,0.37670892,0.6129662],"study_design_scores_gemma":[0.000014179493,0.000035293113,0.00039486305,0.00025793217,0.0000061515216,0.00019520165,0.00005909086,0.00009053986,0.00028854902,0.0013266244,0.9973207,0.000010972487],"about_ca_topic_score_codex":0.0024811316,"about_ca_topic_score_gemma":0.0028151926,"teacher_disagreement_score":0.025651455,"about_ca_system_score_codex":0.00075451884,"about_ca_system_score_gemma":0.0006900576,"threshold_uncertainty_score":0.03658861},"labels":[],"label_agreement":null},{"id":"W4407037568","doi":"10.1111/jns.70002","title":"Hip Dysplasia in Charcot–Marie–Tooth Disease: Insights From a Large Cohort of Children and Adolescents","year":2025,"lang":"en","type":"article","venue":"Journal of the Peripheral Nervous System","topic":"Hereditary Neurological Disorders","field":"Neuroscience","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":"BC Children's Hospital","funders":"University of Melbourne","keywords":"Tooth disease; Cohort; Medicine; Disease; Hip dysplasia; Dentistry; Surgery; Pathology","score_opus":0.0070094674850819175,"score_gpt":0.21933404782892166,"score_spread":0.21232458034383975,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4407037568","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":[0.9990421,0.00036894606,0.000040554358,0.000041974978,0.000003332916,0.000011512974,0.00026741662,0.0000018202398,0.0002222951],"genre_scores_gemma":[0.99815804,0.0009095753,0.00017547811,0.000059456597,0.0000215945,0.000026633728,0.0005195386,0.0000033064928,0.00012652589],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9996598,0.00006724313,0.000038353242,0.00009615511,0.0000827765,0.000055688164],"domain_scores_gemma":[0.99927,0.00012531033,0.00033106186,0.000040942738,0.000096280106,0.00013646537],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0004599743,0.0002577281,0.0003949107,0.0014388437,0.0007110717,0.0007307888,0.00033995812,0.00041344613,0.0011169007],"category_scores_gemma":[0.0013190253,0.00028399492,0.0002877174,0.0013362349,0.00031085993,0.00043480995,0.0006572357,0.00041007303,0.00024003357],"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":[0.00001647199,0.000017380557,0.9979013,0.0000103083785,0.000013675646,0.00051142793,0.00027014912,0.000008005391,0.00013816194,0.000008068485,0.0000966665,0.0010083121],"study_design_scores_gemma":[0.00000317703,0.000043124022,0.99589753,0.000016332075,0.000012026793,0.0029974326,0.00069206354,0.00002050667,0.000023750636,0.000011491928,0.00027999733,0.0000026550954],"about_ca_topic_score_codex":0.007925949,"about_ca_topic_score_gemma":0.012399569,"teacher_disagreement_score":0.007925949,"about_ca_system_score_codex":0.0003248639,"about_ca_system_score_gemma":0.00046162546,"threshold_uncertainty_score":0.015759647},"labels":[],"label_agreement":null},{"id":"W4407387066","doi":"10.1093/ijnp/pyae059.131","title":"TSPO PET BRAIN INFLAMMATION IMAGING: A TRANSDIAGNOSTIC SYSTEMATIC REVIEW AND META-ANALYSIS OF 156 CASE-CONTROL STUDIES","year":2025,"lang":"en","type":"article","venue":"The International Journal of Neuropsychopharmacology","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":1,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Victoria; McGill University; University of British Columbia; University of Toronto; Sunnybrook Health Science Centre","funders":"","keywords":"Meta-analysis; Pet imaging; Medicine; Neuroimaging; Inflammation; Neuroscience; Psychology; Positron emission tomography; Internal medicine","score_opus":0.054891562615826166,"score_gpt":0.3895525625995957,"score_spread":0.3346609999837695,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4407387066","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":[0.017462593,0.97334176,0.0030378124,0.00037086368,0.00023119716,0.0012117794,0.0037947008,0.00008187655,0.00046731578],"genre_scores_gemma":[0.4813948,0.4925209,0.0091164755,0.0020274976,0.0003825343,0.00761829,0.0060310736,0.00014405246,0.000764344],"study_design_codex":"meta_analysis","study_design_gemma":"meta_analysis","domain_scores_codex":[0.9747952,0.010243285,0.008981813,0.002869067,0.0023453317,0.00076524215],"domain_scores_gemma":[0.95818293,0.029777009,0.0064803204,0.0022001432,0.003034342,0.00032521188],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.023151712,0.0027185488,0.01496313,0.009016359,0.001026832,0.003495613,0.0026910002,0.0021219845,0.0039491],"category_scores_gemma":[0.05873995,0.0016923695,0.034141347,0.013753105,0.0011398972,0.0017030232,0.0021125658,0.0016202095,0.000532925],"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":[0.0017961594,0.000030829066,0.01666753,0.36136243,0.6063167,0.00039885144,0.00018477801,0.0006872548,0.00047653003,0.00025656587,0.0012885043,0.010533837],"study_design_scores_gemma":[0.0006113368,0.00016816187,0.0091786655,0.030025803,0.956923,0.0002002823,0.0000827262,0.00023551224,0.00021720461,0.0003146763,0.0020104998,0.000032169755],"about_ca_topic_score_codex":0.0077519673,"about_ca_topic_score_gemma":0.01514528,"teacher_disagreement_score":0.023151712,"about_ca_system_score_codex":0.0031442868,"about_ca_system_score_gemma":0.0051960805,"threshold_uncertainty_score":0.122439384},"labels":[],"label_agreement":null},{"id":"W4407679984","doi":"10.1093/braincomms/fcaf077","title":"Characterization of a novel zebrafish model of <i>MTMR5</i>-associated Charcot-Marie-Tooth disease type 4B3","year":2025,"lang":"en","type":"article","venue":"Brain Communications","topic":"Hereditary Neurological Disorders","field":"Neuroscience","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":"Canada Research Chairs; Hospital for Sick Children; University of Toronto; University of New Brunswick","funders":"Natural Sciences and Engineering Research Council of Canada; Hospital for Sick Children","keywords":"Zebrafish; Tooth disease; Disease; Biology; Neuroscience; Medicine; Genetics; Pathology; Gene","score_opus":0.07992984392513806,"score_gpt":0.3042687243519975,"score_spread":0.2243388804268594,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4407679984","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":[0.9395452,0.0013942854,0.040972788,0.0013895757,0.00028642497,0.0009093075,0.0061383964,0.0013111834,0.0080528995],"genre_scores_gemma":[0.9340883,0.0013606646,0.031647325,0.00049914786,0.000029766577,0.001141316,0.0037064345,0.0005265234,0.02700057],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99964786,0.000026942485,0.000038356626,0.00008872347,0.00013321995,0.00006492795],"domain_scores_gemma":[0.9996468,0.000039991828,0.000113898415,0.0000268662,0.000055861,0.000116546296],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00044691417,0.00081334997,0.0004982012,0.00093772635,0.0007199037,0.0005005152,0.0007951913,0.001325047,0.0037463815],"category_scores_gemma":[0.0003018464,0.00043892648,0.0007660354,0.0001922924,0.0007425698,0.000481189,0.0006162564,0.0015693376,0.0014042304],"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":[0.0000673252,0.000032775937,0.00014069941,0.000041200587,0.000008157626,0.00036093287,0.000040580944,0.000082919134,0.9979073,0.00044551984,0.00018757174,0.00068498834],"study_design_scores_gemma":[0.0002197725,0.0014345543,0.009809034,0.000100802245,0.00014245442,0.0049015568,0.00026865682,0.0043605226,0.95958054,0.00056904,0.018536566,0.00007658507],"about_ca_topic_score_codex":0.0077617443,"about_ca_topic_score_gemma":0.012381487,"teacher_disagreement_score":0.0077617443,"about_ca_system_score_codex":0.0011869977,"about_ca_system_score_gemma":0.0008077707,"threshold_uncertainty_score":0.015433133},"labels":[],"label_agreement":null},{"id":"W4408011640","doi":"10.1016/j.diff.2025.100846","title":"Are vagal neural crest derived tissues impacted in spliceosomopathies?","year":2025,"lang":"en","type":"review","venue":"Differentiation","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":0,"is_retracted":false,"has_abstract":false,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"McGill University; McGill University Health Centre","funders":"Fonds de Recherche du Québec - Santé; Canadian Institutes of Health Research; McGill University","keywords":"Biology; Neural crest; Anatomy; Crest; Zoology; Neural fold; Evolutionary biology; Cell biology; Neural plate; Embryo","score_opus":0.08111179418367241,"score_gpt":0.3467023241177576,"score_spread":0.26559052993408516,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4408011640","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":[0.0001577709,0.9985281,0.00014153664,0.00026443665,0.0001906432,0.0000017301819,0.000025248353,0.0000066500793,0.0006837744],"genre_scores_gemma":[0.0013399774,0.99705493,0.00022783752,0.0003029104,0.00033609674,0.0000039455454,0.000065905,0.0000023189093,0.00066609384],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.99983776,0.000028163493,0.0000346189,0.000034073342,0.000044975313,0.000020489828],"domain_scores_gemma":[0.99977344,0.00012116954,0.000032388034,0.000007824208,0.000046050987,0.000019203977],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0005571816,0.00084136147,0.0013448527,0.0014477031,0.00019184372,0.0011657281,0.0008282106,0.0014517059,0.002418415],"category_scores_gemma":[0.0008544567,0.0002378919,0.00043277585,0.0011494297,0.00059717597,0.0010158767,0.000668364,0.0013695295,0.001376214],"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":[0.00015568864,0.000027592365,0.00056181784,0.010719899,0.00013919831,0.0013591927,0.00006674033,0.00043400505,0.0024926818,0.0044051013,0.028123774,0.9515143],"study_design_scores_gemma":[0.000038560374,0.00006272531,0.0017334482,0.005212055,0.0003769421,0.0075777587,0.0001558892,0.00019037913,0.0013082963,0.004837312,0.9784686,0.00003811168],"about_ca_topic_score_codex":0.0010684757,"about_ca_topic_score_gemma":0.0018103706,"teacher_disagreement_score":0.002418415,"about_ca_system_score_codex":0.0005507851,"about_ca_system_score_gemma":0.0008787362,"threshold_uncertainty_score":0.008090436},"labels":[],"label_agreement":null},{"id":"W4408318097","doi":"10.1055/s-0044-1801500","title":"Die p.(Leu97Ile)-Variante erweitert das genetische Spektrum der NEFL-assoziierten Charcot-Marie-Tooth-Neuropathien","year":2025,"lang":"de","type":"article","venue":"Nervenheilkunde","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":false,"ca_institutions":"Children's Hospital of Eastern Ontario","funders":"","keywords":"Biology","score_opus":0.025103250642218407,"score_gpt":0.2843962996713297,"score_spread":0.25929304902911127,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4408318097","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":[0.9710862,0.009958835,0.006970827,0.0007568832,0.0001847339,0.00032633898,0.004085788,0.00017700306,0.0064534233],"genre_scores_gemma":[0.9847253,0.0030645032,0.0051055867,0.00035990973,0.00009437822,0.0002949208,0.0029893918,0.00005937279,0.003306592],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99942267,0.00010054644,0.00008284674,0.00023591456,0.00009744422,0.0000606126],"domain_scores_gemma":[0.999079,0.00044051817,0.0002420836,0.000084043466,0.00011130053,0.000043001204],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00076504983,0.0011036274,0.0006626128,0.00081992976,0.00035541455,0.0008100839,0.00043568248,0.0010567035,0.0051590605],"category_scores_gemma":[0.002423113,0.00025436026,0.0006036864,0.0008420423,0.00042634294,0.0005186385,0.0004330744,0.0008057066,0.0014824513],"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":[0.0056091244,0.000523646,0.48575354,0.0022206935,0.0007959464,0.085200354,0.0019671384,0.002272089,0.1935175,0.0014300294,0.005444418,0.2152655],"study_design_scores_gemma":[0.00050705427,0.0052256924,0.51007205,0.0013650904,0.0014925791,0.32769424,0.0014056057,0.003967432,0.092288494,0.0030604305,0.052743107,0.00017831501],"about_ca_topic_score_codex":0.0011803686,"about_ca_topic_score_gemma":0.0009920662,"teacher_disagreement_score":0.0051590605,"about_ca_system_score_codex":0.00036201463,"about_ca_system_score_gemma":0.00028613,"threshold_uncertainty_score":0.017258763},"labels":[],"label_agreement":null},{"id":"W4408766989","doi":"10.1101/2025.03.21.25324430","title":"Plasma gangliosides correlate with disease stages and symptom severity in Huntington’s disease carriers","year":2025,"lang":"en","type":"preprint","venue":"medRxiv","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":2,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Calgary; University of Alberta","funders":"","keywords":"Huntington's disease; Disease; Medicine; Immunology; Internal medicine","score_opus":0.017019205493847674,"score_gpt":0.24818888922396112,"score_spread":0.23116968373011346,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4408766989","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":[0.9995931,0.00013427231,0.000049938408,0.000008579076,0.0000015242246,0.0000019338918,0.000077565644,0.000002124718,0.00013098064],"genre_scores_gemma":[0.9996598,0.00003705742,0.000049528193,0.0000051159163,0.0000027071264,0.0000023996438,0.00009874687,9.498386e-7,0.00014369859],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9999292,0.000014918539,0.0000107135065,0.000021841613,0.000011074471,0.00001224582],"domain_scores_gemma":[0.99953127,0.00011247143,0.00019443035,0.000022961758,0.000043880475,0.00009501423],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00022716158,0.0003006347,0.00020357715,0.0007609929,0.0002181029,0.00031881765,0.000095106785,0.00037811432,0.0020521826],"category_scores_gemma":[0.0009416976,0.00014267789,0.00017675356,0.00040091024,0.00020616147,0.00023456638,0.00020996494,0.00025940323,0.0002128557],"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":[0.0006668286,0.000025895963,0.9925141,0.00000999288,0.000053140488,0.00020021816,0.00013136727,0.00004554498,0.0045025656,0.000023720928,0.000058245696,0.0017685038],"study_design_scores_gemma":[0.0000052229966,0.00015058609,0.9986374,0.0000037935652,0.000028690643,0.00044141975,0.00010916552,0.00015513226,0.00033386878,0.000055249795,0.0000765857,0.0000029748842],"about_ca_topic_score_codex":0.0015977055,"about_ca_topic_score_gemma":0.0010129253,"teacher_disagreement_score":0.0020521826,"about_ca_system_score_codex":0.000112211834,"about_ca_system_score_gemma":0.0000833666,"threshold_uncertainty_score":0.006865263},"labels":[],"label_agreement":null},{"id":"W4408992980","doi":"10.1002/iub.70017","title":"Yeast models for Charcot‐Marie‐Tooth disease‐causing aminoacyl‐ <scp>tRNA</scp> synthetase alleles reveal the cellular basis of disease","year":2025,"lang":"en","type":"review","venue":"IUBMB Life","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":6,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"Children’s Health Research Institute; Western University","funders":"Ontario Ministry of Research and Innovation; Natural Sciences and Engineering Research Council of Canada; Canadian Institutes of Health Research","keywords":"Allele; Yeast; Tooth disease; Disease; Aminoacyl tRNA synthetase; Biology; Genetics; Saccharomyces cerevisiae; Transfer RNA; Microbiology; Gene; Medicine; RNA; Pathology","score_opus":0.08978397880243857,"score_gpt":0.3055848530806925,"score_spread":0.21580087427825392,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4408992980","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":[0.00020101474,0.9971987,0.00018754817,0.00015598533,0.00014348775,0.0000055203013,0.00005403803,0.000023001343,0.0020307282],"genre_scores_gemma":[0.0007816378,0.9978242,0.00026089227,0.00011753495,0.00004127963,0.0000095012965,0.00008342762,0.0000031605773,0.0008783716],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.99992526,0.000009664964,0.000011048287,0.000013854538,0.00003202521,0.000008046482],"domain_scores_gemma":[0.99990845,0.00003229814,0.000014160347,0.0000045704346,0.000026531165,0.00001394963],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00026171553,0.00068670395,0.00076793355,0.0013082201,0.00017714889,0.0006455265,0.0005944941,0.0006252281,0.0024667752],"category_scores_gemma":[0.00024983706,0.00016534347,0.00032002205,0.0011581321,0.00022908609,0.0006959533,0.0004580906,0.0010604771,0.002791739],"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":[0.00009695077,0.000058106663,0.00018313261,0.0152132,0.00007660387,0.00026218328,0.00005022827,0.00029129157,0.0074255946,0.0065638092,0.04355222,0.9262267],"study_design_scores_gemma":[0.000009316283,0.000053995616,0.0005324411,0.0013358883,0.000075399694,0.0007423651,0.000027814818,0.000048472633,0.00096045504,0.0011982438,0.99500483,0.000010749637],"about_ca_topic_score_codex":0.0008628376,"about_ca_topic_score_gemma":0.0014325291,"teacher_disagreement_score":0.0024667752,"about_ca_system_score_codex":0.00044725658,"about_ca_system_score_gemma":0.00057654304,"threshold_uncertainty_score":0.008252144},"labels":[],"label_agreement":null},{"id":"W4409344801","doi":"10.3389/fnins.2025.1595717","title":"Editorial: Translational research in hereditary spastic paraplegias: filling the diagnosis gap and therapeutic perspectives","year":2025,"lang":"en","type":"editorial","venue":"Frontiers in Neuroscience","topic":"Hereditary Neurological Disorders","field":"Neuroscience","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":"Hereditary spastic paraplegia; Medicine; Spastic; Translational research; Psychology; Physical medicine and rehabilitation; Pathology; Biology; Genetics","score_opus":0.06955252761062213,"score_gpt":0.34588670072889066,"score_spread":0.2763341731182685,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4409344801","genre_codex":"editorial","genre_gemma":"editorial","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"editorial","genre_consensus":"editorial","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.000084171406,0.0030826803,0.00014245526,0.033786096,0.962174,0.000025159045,0.000054490767,0.00009912926,0.0005518419],"genre_scores_gemma":[0.0003341463,0.002013509,0.00008945579,0.018173177,0.9776159,0.0000150262895,0.000024047875,0.000028007342,0.001706714],"study_design_codex":"not_applicable","study_design_gemma":"not_applicable","domain_scores_codex":[0.9937441,0.0011942128,0.00086175377,0.0009697056,0.0026295532,0.00060072937],"domain_scores_gemma":[0.96786356,0.014398908,0.0020517893,0.00090209325,0.010186035,0.0045976294],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.010086386,0.0045819627,0.0054305294,0.0032995513,0.0036069741,0.009271609,0.006138601,0.02101826,0.017063653],"category_scores_gemma":[0.026876315,0.0015292576,0.0038301377,0.0015670238,0.0038720237,0.0069757197,0.0016977943,0.024593709,0.010337631],"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":[0.0001636769,0.0000582402,0.00008578858,0.0005156736,0.00004283802,0.0001907113,0.00002403467,0.000063385094,0.0001383733,0.00043665658,0.9912135,0.0070672124],"study_design_scores_gemma":[0.00030202753,0.00018207531,0.0008463454,0.0009944162,0.00013499458,0.00054707413,0.00012347472,0.0006285568,0.00033332742,0.0021460222,0.99369955,0.00006209522],"about_ca_topic_score_codex":0.0011936835,"about_ca_topic_score_gemma":0.0021756846,"teacher_disagreement_score":0.02101826,"about_ca_system_score_codex":0.0031717615,"about_ca_system_score_gemma":0.0031632443,"threshold_uncertainty_score":0.057083607},"labels":[],"label_agreement":null},{"id":"W4409823778","doi":"10.1002/jcsm.13815","title":"Myo‐Guide: A Machine Learning‐Based Web Application for Neuromuscular Disease Diagnosis With MRI","year":2025,"lang":"en","type":"article","venue":"Journal of Cachexia Sarcopenia and Muscle","topic":"Hereditary Neurological Disorders","field":"Neuroscience","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":"Ottawa Hospital; Children's Hospital of Eastern Ontario","funders":"NIHR Newcastle Biomedical Research Centre; Muscular Dystrophy UK; Department of Health and Social Care; Jain Foundation; Newcastle University; National Institute for Health and Care Research","keywords":"Medicine; Sarcopenia; Machine learning; Muscle weakness; Magnetic resonance imaging; Limiting; Disease; Muscle disorder; Artificial intelligence; Bioinformatics; Pathology; Computer science; Radiology; Internal medicine; Biology","score_opus":0.013497003351539968,"score_gpt":0.26369857317873685,"score_spread":0.2502015698271969,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4409823778","genre_codex":"software","genre_gemma":"software","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"software","genre_consensus":"software","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.013493854,0.0019135593,0.23459661,0.001015511,0.00024252252,0.00084762863,0.049370047,0.6921164,0.0064039626],"genre_scores_gemma":[0.18147017,0.0026918815,0.6175215,0.004013356,0.00033951746,0.0035770498,0.14593725,0.025320133,0.01912913],"study_design_codex":"not_applicable","study_design_gemma":"simulation_or_modeling","domain_scores_codex":[0.99956506,0.000100136625,0.00005304155,0.00013716232,0.00011435623,0.000030167452],"domain_scores_gemma":[0.99863607,0.0008725385,0.00011175299,0.0001179188,0.00013921208,0.00012251912],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0012163074,0.0014408214,0.0006614314,0.002282396,0.0002432558,0.0008420793,0.0016792373,0.0013379642,0.02334474],"category_scores_gemma":[0.004232737,0.0005279233,0.0009517949,0.0010021381,0.00020430968,0.00092019694,0.0017573552,0.0010142704,0.012904932],"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":[0.0014213714,0.00045256957,0.012420864,0.002311505,0.00068268616,0.0016519469,0.0002721579,0.022345481,0.008443349,0.0024899945,0.48370686,0.4638012],"study_design_scores_gemma":[0.0011736002,0.0003895469,0.018977907,0.00064479257,0.00023118155,0.0027348625,0.00017001758,0.6167933,0.017513102,0.026547203,0.3145404,0.0002841565],"about_ca_topic_score_codex":0.0023324047,"about_ca_topic_score_gemma":0.0045769066,"teacher_disagreement_score":0.02334474,"about_ca_system_score_codex":0.00046766357,"about_ca_system_score_gemma":0.00088991504,"threshold_uncertainty_score":0.07809591},"labels":[],"label_agreement":null},{"id":"W4410097135","doi":"10.1002/mdc3.70115","title":"Hereditary Spastic Paraplegia in Alberta: Lessons from a Well‐Defined Cohort Including the Indigenous Population","year":2025,"lang":"en","type":"article","venue":"Movement Disorders Clinical Practice","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":1,"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; University of Alberta; University of Calgary","funders":"Canadian Institutes of Health Research","keywords":"Hereditary spastic paraplegia; Indigenous; Medicine; Population; Genetic testing; Cohort; Ethnic group; Genetics; Internal medicine; Phenotype; Biology; Gene; Environmental health","score_opus":0.061623768848125066,"score_gpt":0.38629412200093216,"score_spread":0.3246703531528071,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4410097135","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":[0.9904246,0.0018981631,0.00028820944,0.0010050687,0.00006772025,0.000087804496,0.00144338,0.00002136993,0.0047636717],"genre_scores_gemma":[0.9941953,0.0026925416,0.000396721,0.00038853695,0.000059803988,0.000035618283,0.0013368079,0.000016558462,0.0008780513],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99910057,0.00013054507,0.000055921122,0.00018987602,0.00024663817,0.00027637763],"domain_scores_gemma":[0.99808276,0.00021039888,0.00022854727,0.00017532957,0.0007426774,0.0005602295],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.001517666,0.0006925823,0.00060907006,0.0016280698,0.002927816,0.0018394574,0.0015904625,0.00076640304,0.0016807705],"category_scores_gemma":[0.0024641743,0.0003209307,0.00045673497,0.0034180684,0.001001815,0.0006088008,0.0012422423,0.0007758459,0.00023517101],"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":[0.00015816485,0.00007830214,0.9841176,0.00004339379,0.000068390844,0.0016480245,0.0032753323,0.00008391905,0.0002856162,0.00015786376,0.0014133567,0.008669956],"study_design_scores_gemma":[0.000017345314,0.000056452736,0.9938693,0.000080938655,0.00006149213,0.00060545746,0.0036945757,0.00013556107,0.00003228289,0.00009914673,0.0013303485,0.000016910079],"about_ca_topic_score_codex":0.92456275,"about_ca_topic_score_gemma":0.93378675,"teacher_disagreement_score":0.07543725,"about_ca_system_score_codex":0.0071022604,"about_ca_system_score_gemma":0.009557323,"threshold_uncertainty_score":0.15176296},"labels":[],"label_agreement":null},{"id":"W4410616544","doi":"10.1016/j.msard.2025.106544","title":"Navigating a paradigm shift in the treatment of CNS demyelinating diseases in a middle-income country","year":2025,"lang":"en","type":"article","venue":"Multiple Sclerosis and Related Disorders","topic":"Hereditary Neurological Disorders","field":"Neuroscience","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":"Multiple sclerosis; Medicine; Demyelinating disease; Paradigm shift; Low and middle income countries; Neuroscience; Developing country; Immunology; Economic growth; Psychology; Economics","score_opus":0.03399252837059849,"score_gpt":0.2637806442357036,"score_spread":0.22978811586510509,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4410616544","genre_codex":"commentary","genre_gemma":"commentary","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"commentary","genre_consensus":"commentary","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.017740456,0.014286928,0.0016405965,0.9558056,0.003516024,0.000025595697,0.00008326878,0.000032480773,0.0068689934],"genre_scores_gemma":[0.33269525,0.061879143,0.013708679,0.5720807,0.012797602,0.00023222464,0.00033657465,0.000119078766,0.006150771],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.9954058,0.0019962124,0.00037782724,0.00028508584,0.00059281604,0.0013422248],"domain_scores_gemma":[0.9902181,0.0016156818,0.0008125991,0.00019400787,0.0013711539,0.005788427],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.010565427,0.0003861549,0.0008771318,0.00092948414,0.0038425494,0.007872556,0.002193356,0.005365879,0.008549624],"category_scores_gemma":[0.008386879,0.00022637587,0.000693544,0.0008371526,0.004438478,0.00615303,0.009945509,0.009922421,0.0012042663],"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":[0.0012350372,0.0033220737,0.02686545,0.004074723,0.0003669038,0.0060811187,0.00993916,0.0025735216,0.0064611486,0.19530988,0.31321913,0.4305519],"study_design_scores_gemma":[0.00071908935,0.0019484014,0.04491831,0.008273862,0.00026377413,0.0039087376,0.033269767,0.0017892527,0.0013566228,0.11367885,0.78958493,0.0002884534],"about_ca_topic_score_codex":0.018791616,"about_ca_topic_score_gemma":0.03778567,"teacher_disagreement_score":0.018791616,"about_ca_system_score_codex":0.0054756487,"about_ca_system_score_gemma":0.04300421,"threshold_uncertainty_score":0.055876017},"labels":[],"label_agreement":null},{"id":"W4412162315","doi":"10.1101/2025.07.05.24312261","title":"Digenic inheritance of mutations in <i>SPG7</i> and <i>AFG3L2</i> causes motor neuron and cerebellar disorders","year":2025,"lang":"en","type":"preprint","venue":"medRxiv","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":0,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of Alberta; Alberta Children's Hospital; McGill University; University of Ottawa; Montreal Neurological Institute and Hospital","funders":"Canadian Institutes of Health Research; Parkinson Canada","keywords":"Inheritance (genetic algorithm); Motor neuron; Genetics; Medicine; Biology; Neuroscience; Gene","score_opus":0.024463195933239736,"score_gpt":0.2629986023047574,"score_spread":0.23853540637151768,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4412162315","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":[0.9982236,0.00019731394,0.000431974,0.000023170454,0.000005618888,0.000009915888,0.0006763241,0.000017274544,0.00041485645],"genre_scores_gemma":[0.9984445,0.000117000345,0.00042624873,0.000049397313,0.000006612849,0.000006180058,0.00076349743,0.00000704956,0.00017946975],"study_design_codex":"observational","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99959415,0.00004086893,0.00006233367,0.00019007351,0.000067032415,0.000045567376],"domain_scores_gemma":[0.9996573,0.00010443418,0.00012430981,0.000027558477,0.000026165699,0.000060224367],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00021494961,0.00045088923,0.00034135344,0.0014780761,0.0004909608,0.0003827076,0.00024358374,0.0003221959,0.0024803116],"category_scores_gemma":[0.0006242451,0.000163415,0.00034759162,0.0010894877,0.00028918154,0.0001249616,0.0004719446,0.00024641675,0.00022524125],"study_design_candidate":"bench_or_experimental","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0007790784,0.00008598294,0.83149713,0.00012299386,0.00058750325,0.018261572,0.00025439655,0.00033616586,0.13266364,0.0004452871,0.00075029745,0.014215987],"study_design_scores_gemma":[0.000038215312,0.00013708511,0.9707554,0.00003109512,0.00028892068,0.019362638,0.00016122349,0.0008961231,0.006455912,0.00031947225,0.0015356034,0.000018349727],"about_ca_topic_score_codex":0.0019398024,"about_ca_topic_score_gemma":0.004289387,"teacher_disagreement_score":0.0024803116,"about_ca_system_score_codex":0.00019673262,"about_ca_system_score_gemma":0.0001840506,"threshold_uncertainty_score":0.008297443},"labels":[],"label_agreement":null},{"id":"W4412195273","doi":"10.3390/s25144312","title":"Plantar Pressure Distribution in Charcot–Marie–Tooth Disease: A Systematic Review","year":2025,"lang":"en","type":"review","venue":"Sensors","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":2,"is_retracted":false,"has_abstract":true,"route_ca_aff":false,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":true,"ca_institutions":"","funders":"","keywords":"Forefoot; Plantar pressure; Medicine; Physical medicine and rehabilitation; Tooth disease; Center of pressure (fluid mechanics); Foot Orthoses; Gait; Disease; Physical therapy; Surgery; Internal medicine; Pressure sensor; Complication","score_opus":0.03893270298410692,"score_gpt":0.3136863946594384,"score_spread":0.2747536916753315,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4412195273","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":[0.0009791582,0.9983367,0.00006537417,0.00009078383,0.00005241708,0.00008092898,0.00024952734,0.000004985897,0.00014010143],"genre_scores_gemma":[0.013218545,0.9858849,0.00022984981,0.00017679353,0.000046926107,0.00018205798,0.00019161368,0.0000032426785,0.00006597987],"study_design_codex":"systematic_review","study_design_gemma":"systematic_review","domain_scores_codex":[0.996772,0.00095620076,0.0012293338,0.00032237737,0.000591158,0.00012893454],"domain_scores_gemma":[0.98718137,0.009228868,0.0022749559,0.00015487942,0.0010126738,0.00014728523],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0035642546,0.0014142152,0.007111614,0.009375263,0.0004805924,0.0021999478,0.001604931,0.0015228427,0.003953298],"category_scores_gemma":[0.017761562,0.000780749,0.005180531,0.010037001,0.0005888226,0.0015986718,0.0012268119,0.0006870839,0.00026910022],"study_design_candidate":"systematic_review","study_design_consensus":"systematic_review","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00015432676,0.000011096752,0.0006433441,0.963663,0.0063406522,0.00009791491,0.00010591459,0.00006977765,0.00011405307,0.00010168188,0.0010687129,0.027629718],"study_design_scores_gemma":[0.00025773942,0.00029525236,0.00791452,0.8856762,0.086295046,0.0009314384,0.00036536335,0.00010739711,0.00020506904,0.00027992428,0.017623598,0.000048488666],"about_ca_topic_score_codex":0.006770867,"about_ca_topic_score_gemma":0.016190229,"teacher_disagreement_score":0.009375263,"about_ca_system_score_codex":0.0021491374,"about_ca_system_score_gemma":0.0062160054,"threshold_uncertainty_score":0.01884979},"labels":[],"label_agreement":null},{"id":"W4412520970","doi":"10.1016/s1474-4422(25)00198-x","title":"Acute-onset axonal neuropathy following infection in children with biallelic RCC1 variants: a case series","year":2025,"lang":"en","type":"article","venue":"The Lancet Neurology","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":1,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":true,"ca_institutions":"Children's Hospital of Eastern Ontario","funders":"Medical Research Council; Manchester Biomedical Research Centre; Department of Health and Social Care; National Institute for Health and Care Research; Heart of England NHS Foundation Trust; Cancer Research UK; LifeArc; Research Trainees Coordinating Centre; University of Manchester; Wellcome Trust","keywords":"Missense mutation; Exome sequencing; Medicine; Phenotype; Exome; Pathology; Biology; Genetics; Gene","score_opus":0.021564009943141317,"score_gpt":0.26586161634917516,"score_spread":0.24429760640603385,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4412520970","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":[0.9973821,0.0006616055,0.0005360546,0.0001464814,0.000025820415,0.00005590997,0.00010211997,0.00002624184,0.0010637605],"genre_scores_gemma":[0.9988129,0.00033898428,0.000424201,0.00008537507,0.00004975787,0.000013554405,0.00007121683,0.000009085395,0.0001949127],"study_design_codex":"case_report","study_design_gemma":"case_report","domain_scores_codex":[0.99898523,0.00008743401,0.00014842903,0.0003359244,0.00016663005,0.00027645618],"domain_scores_gemma":[0.9981401,0.0005152798,0.00056859636,0.00012337448,0.00014171783,0.00051092065],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00040933344,0.0016729445,0.000880563,0.001439801,0.0021673753,0.0010717956,0.00085135305,0.0018794172,0.002091389],"category_scores_gemma":[0.0020892005,0.00093725795,0.00070211885,0.0014898628,0.0014122468,0.0009503546,0.001357687,0.0012870553,0.00043204235],"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":[0.000096736854,0.00008164882,0.1652187,0.00008657826,0.00005253962,0.8277161,0.0010621177,0.00010607729,0.0018231795,0.00013286511,0.00040952992,0.0032138291],"study_design_scores_gemma":[0.000012370939,0.00011986811,0.04892178,0.000022004466,0.000030050336,0.94966483,0.00048983685,0.00009901873,0.00028772774,0.000040659612,0.00029696146,0.000014842862],"about_ca_topic_score_codex":0.004848487,"about_ca_topic_score_gemma":0.0066700936,"teacher_disagreement_score":0.004848487,"about_ca_system_score_codex":0.0010450698,"about_ca_system_score_gemma":0.0007801006,"threshold_uncertainty_score":0.009640515},"labels":[],"label_agreement":null},{"id":"W4412817158","doi":"10.1111/ene.70313","title":"Nationwide Phenotypic and Genotypic Characterisation of 103 Patients With <i>SH3TC2</i> Gene‐Related Demyelinating Peripheral Neuropathy","year":2025,"lang":"en","type":"article","venue":"European Journal of Neurology","topic":"Hereditary Neurological Disorders","field":"Neuroscience","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":"Hotel Dieu Hospital","funders":"","keywords":"Medicine; Scoliosis; Weakness; Age of onset; Sensory loss; Peripheral neuropathy; Retrospective cohort study; Pediatrics; Compound heterozygosity; Internal medicine; Disease; Surgery; Phenotype; Genetics; Endocrinology; Gene; Diabetes mellitus","score_opus":0.008330197263644996,"score_gpt":0.20330965292008432,"score_spread":0.19497945565643932,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4412817158","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":[0.99957675,0.00006227892,0.000050093135,0.000008616719,0.000001042913,0.00000567132,0.00015010388,0.0000030676135,0.00014238546],"genre_scores_gemma":[0.99930084,0.00005314402,0.00007972318,0.000027286578,0.000004682482,0.000009494355,0.00045849814,0.0000018098326,0.0000645309],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9995726,0.00007111686,0.000044069035,0.00013673483,0.00007200281,0.00010356339],"domain_scores_gemma":[0.99926466,0.00014373689,0.0002834349,0.00005060376,0.00011141022,0.00014620274],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00034455332,0.00041431532,0.00036376674,0.0007098649,0.00055283104,0.0004576098,0.00029809485,0.00049091235,0.001137896],"category_scores_gemma":[0.0011705875,0.00030561336,0.0003228013,0.00057362835,0.00034893726,0.00022224571,0.00038894868,0.0002809801,0.00026286888],"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":[0.00007616626,0.000034508506,0.9953424,0.000008077598,0.000021146712,0.0016717575,0.00014595728,0.000031171854,0.001095652,0.000008196488,0.000103000966,0.0014620073],"study_design_scores_gemma":[0.000016648284,0.00019973416,0.9917989,0.0000058155642,0.000020976815,0.007150747,0.00018181565,0.00009331741,0.00024890146,0.000007877558,0.00026964975,0.000005672256],"about_ca_topic_score_codex":0.008643638,"about_ca_topic_score_gemma":0.006516822,"teacher_disagreement_score":0.008643638,"about_ca_system_score_codex":0.0005128183,"about_ca_system_score_gemma":0.00036454262,"threshold_uncertainty_score":0.017186642},"labels":[],"label_agreement":null},{"id":"W4413339166","doi":"10.1002/mds.70006","title":"Spastic Ataxia Composite ( <scp>SPAXCOM</scp> ): A Scale to Evaluate the Progression of Subjects with Spasticity and Ataxia","year":2025,"lang":"en","type":"article","venue":"Movement Disorders","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":1,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":true,"ca_institutions":"Centres Intégré Universitaires de Santé et de Services Sociaux; Cégep de Jonquière; Montreal Neurological Institute and Hospital; McGill University; Centre Intégré Universitaire de Santé et de Services Sociaux du Saguenay–Lac-Saint-Jean; Université de Sherbrooke","funders":"NIHR Cambridge Biomedical Research Centre; National Medical Research Council; Medical Research Council; Ministero della Salute; Else Kröner-Fresenius-Stiftung; National Institute for Health and Care Research; Bundesministerium für Bildung und Forschung; Eberhard Karls Universität Tübingen; HORIZON EUROPE Framework Programme; Wellcome Trust; Agence Nationale de la Recherche; Ataxia UK; Deutsche Forschungsgemeinschaft; UK Research and Innovation; Department of Health and Social Care; ZonMw; LifeArc","keywords":"Ataxia; Spasticity; Spastic; Rating scale; Spinocerebellar ataxia; Medicine; Physical therapy; Physical medicine and rehabilitation; Modified Ashworth scale; Psychology; Cerebral palsy; Psychiatry; Developmental psychology","score_opus":0.014527557297946738,"score_gpt":0.26713558875536997,"score_spread":0.2526080314574232,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4413339166","genre_codex":"empirical","genre_gemma":"methods","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"methods","genre_consensus":null,"domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.9605387,0.0022141424,0.0058262665,0.00035888815,0.00017320439,0.002861059,0.012359646,0.00042338466,0.015244589],"genre_scores_gemma":[0.96211946,0.00097049,0.019157436,0.0002704312,0.00008391385,0.002655662,0.011282334,0.00005155996,0.0034086693],"study_design_codex":"observational","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9978465,0.00057787413,0.00043889874,0.00018315853,0.00084095105,0.00011258101],"domain_scores_gemma":[0.99364096,0.0014511842,0.0026731137,0.00026629196,0.0015463228,0.00042212193],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0029736424,0.0008078372,0.0008282737,0.0023177378,0.00041096724,0.0005065922,0.0006440986,0.0006819366,0.0034975773],"category_scores_gemma":[0.0065729404,0.00020710914,0.001254334,0.0011590967,0.00035397796,0.000687667,0.0011637078,0.0008110003,0.0007421712],"study_design_candidate":"bench_or_experimental","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0024364567,0.0006287783,0.8679145,0.0010654973,0.0015270093,0.00030230012,0.0007431141,0.0017310239,0.005369158,0.00061921397,0.01472758,0.10293536],"study_design_scores_gemma":[0.00013628336,0.0009024901,0.9923228,0.00009049515,0.00010536295,0.0005626103,0.00013561502,0.00084288075,0.00053315,0.00021032167,0.004128733,0.000029275485],"about_ca_topic_score_codex":0.0028439627,"about_ca_topic_score_gemma":0.007217038,"teacher_disagreement_score":0.0034975773,"about_ca_system_score_codex":0.0006131814,"about_ca_system_score_gemma":0.00066880905,"threshold_uncertainty_score":0.015726328},"labels":[],"label_agreement":null},{"id":"W4413343636","doi":"10.1093/brain/awaf300","title":"Biallelic variants in <i>COX18</i> cause a mitochondrial disorder primarily manifesting as peripheral neuropathy","year":2025,"lang":"en","type":"article","venue":"Brain","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":0,"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; NIHR Great Ormond Street Hospital Biomedical Research Centre; Horizon 2020; Seventh Framework Programme; Universiteit Antwerpen; Medical Research Council Canada; Muscular Dystrophy Association; Association Belge contre les Maladies Neuro-Musculaires; Fonds Wetenschappelijk Onderzoek; Vlaamse regering; Fonds De La Recherche Scientifique - FNRS; Harrington Discovery Institute, University Hospitals; Wellcome Trust; AFM-Téléthon; Charcot-Marie-Tooth Association","keywords":"Biology; Exome sequencing; Compound heterozygosity; Exon; Mitochondrial respiratory chain; Genetics; Mitochondrial disease; Exome; Mitochondrion; Molecular biology; Mutation; Gene; Mitochondrial DNA","score_opus":0.020602441903181903,"score_gpt":0.2746443727756089,"score_spread":0.254041930872427,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4413343636","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":[0.99551916,0.0005508547,0.0024351694,0.00010617374,0.00003687135,0.00002364824,0.00047698471,0.00008259583,0.0007684089],"genre_scores_gemma":[0.9971666,0.00024205979,0.0014279684,0.000064833665,0.000052236697,0.000010845294,0.00044167368,0.000030005422,0.00056391314],"study_design_codex":"bench_or_experimental","study_design_gemma":"case_report","domain_scores_codex":[0.9998337,0.000018209466,0.000026077936,0.00005747762,0.00003995874,0.000024527877],"domain_scores_gemma":[0.9995915,0.00007075372,0.00022532456,0.00002126729,0.000027101356,0.00006409536],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00010872301,0.00093824393,0.00028796276,0.00043918975,0.00032466266,0.00022116194,0.00030432653,0.0005385112,0.002804176],"category_scores_gemma":[0.00035367793,0.0001425922,0.00032015904,0.00037899017,0.00029103356,0.00010869617,0.00031709645,0.0004611665,0.0006853503],"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":[0.0012608469,0.00016132883,0.124153905,0.00024605036,0.00031496564,0.08367276,0.0005412073,0.0004065151,0.7681248,0.0006363652,0.0011518057,0.019329423],"study_design_scores_gemma":[0.00020049582,0.0009733008,0.42820528,0.0001596944,0.00057249365,0.3758669,0.0005091395,0.00246193,0.17599693,0.00068788655,0.014305574,0.00006046221],"about_ca_topic_score_codex":0.00056798384,"about_ca_topic_score_gemma":0.0011241292,"teacher_disagreement_score":0.002804176,"about_ca_system_score_codex":0.00016602692,"about_ca_system_score_gemma":0.0001237417,"threshold_uncertainty_score":0.009380937},"labels":[],"label_agreement":null},{"id":"W4413756731","doi":"10.37381/jpga7419","title":"Torticles","year":2019,"lang":"en","type":"article","venue":"Tulane European and Civil Law Forum","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":false,"ca_institutions":"Trinity College","funders":"","keywords":"Psychology","score_opus":0.014961864536137669,"score_gpt":0.20985500037350094,"score_spread":0.19489313583736326,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4413756731","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":[0.0036203174,0.005975476,0.002823128,0.06558826,0.024990827,0.00026934608,0.00076078734,0.0006620771,0.8953096],"genre_scores_gemma":[0.023509456,0.0014251758,0.0007015369,0.05893613,0.0028089336,0.0001567171,0.00034441758,0.00022192865,0.91189563],"study_design_codex":"not_applicable","study_design_gemma":"not_applicable","domain_scores_codex":[0.99086106,0.0011761183,0.0004230256,0.0015499139,0.004285132,0.0017047565],"domain_scores_gemma":[0.9943129,0.0022643826,0.00031588253,0.00067919784,0.0018628897,0.00056483457],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0047325627,0.001077616,0.0010151308,0.0017997589,0.0094139315,0.009170558,0.0023931775,0.016153647,0.0799755],"category_scores_gemma":[0.022114698,0.00090738625,0.0016922898,0.00082978094,0.002652329,0.0029897701,0.004477313,0.018260866,0.031305656],"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":[0.00005355805,0.00006276714,0.00056762417,0.00006726198,0.000019803389,0.0006832817,0.00041463392,0.00008960453,0.00041533975,0.17569093,0.80068547,0.021249725],"study_design_scores_gemma":[0.000010554116,0.000017110871,0.0005927532,0.000116105744,0.000013267288,0.00027759004,0.00020634486,0.0001465728,0.0002632989,0.0062022973,0.9921359,0.000018141063],"about_ca_topic_score_codex":0.017030982,"about_ca_topic_score_gemma":0.025416598,"teacher_disagreement_score":0.0799755,"about_ca_system_score_codex":0.0036252695,"about_ca_system_score_gemma":0.005945174,"threshold_uncertainty_score":0},"labels":[],"label_agreement":null},{"id":"W4414002673","doi":"10.1016/j.nmd.2025.106213","title":"Surgical correction of foot deformities in Charcot-Marie-Tooth-disease: effects on personal goals and gait capacity","year":2025,"lang":"en","type":"article","venue":"Neuromuscular Disorders","topic":"Hereditary Neurological Disorders","field":"Neuroscience","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":"ZonMw","keywords":"Tooth disease; Gait; Foot (prosody); Physical medicine and rehabilitation; Medicine; Disease; Pathology; Art","score_opus":0.012603160057064928,"score_gpt":0.23487933897579052,"score_spread":0.2222761789187256,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4414002673","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":[0.9992249,0.00036508663,0.00003078332,0.000014360245,0.0000017504357,0.000002753588,0.000016164686,0.0000017326926,0.0003425154],"genre_scores_gemma":[0.99961936,0.00015516313,0.0000670212,0.0000067160263,0.0000016317019,0.000002286264,0.00003061734,5.3940477e-7,0.00011668134],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9998042,0.000052671297,0.000017800256,0.000016842741,0.00006801821,0.000040542393],"domain_scores_gemma":[0.9996178,0.00009964852,0.00010125695,0.000019845607,0.000040541403,0.00012089192],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0003198192,0.0001778884,0.0001963097,0.00030193388,0.00025902264,0.00018126058,0.00012170123,0.00016730653,0.0005344047],"category_scores_gemma":[0.0011695448,0.000048861228,0.0002268869,0.00020764637,0.0002400537,0.00011168174,0.00024872832,0.00015798456,0.00006404437],"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":[0.0027227954,0.0020122142,0.8414762,0.00014335875,0.00028701007,0.0027718719,0.00064587867,0.000826561,0.013913504,0.00007648848,0.0003549075,0.13476923],"study_design_scores_gemma":[0.0000085618585,0.00085409736,0.99753845,0.0000073360047,0.000018212057,0.00084913464,0.00012144445,0.00010363393,0.00036036273,0.000023277253,0.000111236106,0.0000043234327],"about_ca_topic_score_codex":0.0044640107,"about_ca_topic_score_gemma":0.009006718,"teacher_disagreement_score":0.0044640107,"about_ca_system_score_codex":0.00032440122,"about_ca_system_score_gemma":0.00022504677,"threshold_uncertainty_score":0.008876026},"labels":[],"label_agreement":null},{"id":"W4414885856","doi":"10.1093/braincomms/fcaf382","title":"Mild cognitive dysfunction in hereditary spastic paraplegia 4 disease related to fluorodesoxyglucose cerebral positron emission tomography","year":2025,"lang":"en","type":"article","venue":"Brain Communications","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":1,"is_retracted":false,"has_abstract":true,"route_ca_aff":false,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":true,"ca_institutions":"","funders":"","keywords":"Hereditary spastic paraplegia; Population; Cognitive decline; Cognition; Neuropsychology; Dementia; Memory span; Neuropsychological assessment; Verbal memory","score_opus":0.028706228556340894,"score_gpt":0.301941688824076,"score_spread":0.2732354602677351,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4414885856","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":[0.99920124,0.00016185213,0.00008488152,0.000021419635,0.000005462879,0.000007206765,0.000051859428,0.00000675214,0.00045926307],"genre_scores_gemma":[0.9995357,0.000067564324,0.000048387556,0.00002390433,0.000014615252,0.0000035645091,0.00007760366,0.0000015507247,0.00022708776],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99988484,0.000027927657,0.000010967449,0.000022822405,0.000019487852,0.000033982073],"domain_scores_gemma":[0.9997732,0.00006315335,0.00006098018,0.000013051385,0.000031012605,0.00005860996],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0002525332,0.0010414599,0.00035466146,0.0010421129,0.0003917235,0.0002905138,0.00020806692,0.0004220442,0.0025048438],"category_scores_gemma":[0.00075474364,0.00024410058,0.0002605665,0.00030441847,0.00046533122,0.00018800543,0.0003409677,0.00023613898,0.00027146476],"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":[0.001605827,0.00024455006,0.8785427,0.00007616462,0.00015336425,0.09209605,0.00035050794,0.00021614977,0.019369012,0.00011664754,0.0005176594,0.006711288],"study_design_scores_gemma":[0.000049734328,0.00081814756,0.9363544,0.000016749078,0.000071331415,0.06049265,0.0001555711,0.0004152733,0.001077955,0.00010652796,0.00042981445,0.0000117504],"about_ca_topic_score_codex":0.003575767,"about_ca_topic_score_gemma":0.0038389901,"teacher_disagreement_score":0.003575767,"about_ca_system_score_codex":0.00027632303,"about_ca_system_score_gemma":0.00019725271,"threshold_uncertainty_score":0.008379579},"labels":[],"label_agreement":null},{"id":"W4415269065","doi":"10.1101/2025.10.15.682364","title":"Gene therapy-mediated overexpression of wild-type MFN2 improves Charcot-Marie-Tooth disease type 2A","year":2025,"lang":"en","type":"preprint","venue":"bioRxiv (Cold Spring Harbor Laboratory)","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":false,"ca_institutions":"Canadian Nautical Research Society","funders":"École Polytechnique Fédérale de Lausanne; Institut National de la Santé et de la Recherche Médicale; Agence Nationale de la Recherche","keywords":"MFN2; Endoplasmic reticulum; Genetic enhancement; Mitochondrion; Transgene; Gene; Viral vector; Genetically modified mouse; mitochondrial fusion","score_opus":0.024469245999224235,"score_gpt":0.2408886673873906,"score_spread":0.21641942138816636,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4415269065","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":[0.9859833,0.0035852103,0.0052449936,0.00033643207,0.00030923085,0.0001299191,0.0007514672,0.00052732835,0.0031320439],"genre_scores_gemma":[0.9883576,0.002339144,0.0031771397,0.0001288798,0.00005103295,0.00013217714,0.0007022349,0.000064142994,0.0050477376],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9998252,0.000020556154,0.000018264443,0.00004426148,0.000057441404,0.000034292043],"domain_scores_gemma":[0.9999268,0.000008939863,0.000020004863,0.0000061023843,0.000010004354,0.000028071609],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00020796932,0.0006913797,0.0005088952,0.00046679378,0.0001857629,0.0003891629,0.00026744662,0.00074380066,0.0015392137],"category_scores_gemma":[0.000117299474,0.0001172525,0.00035970268,0.00018378388,0.00034489858,0.00037899325,0.00019132256,0.0009945333,0.00038211665],"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":[0.00021371733,0.00021797055,0.00005118378,0.000080344274,0.000012643876,0.00005525658,0.000018280167,0.00012707686,0.9961289,0.00011608213,0.00016107586,0.0028175442],"study_design_scores_gemma":[0.00020668855,0.0043112217,0.003428316,0.00003183911,0.00008841211,0.0006189124,0.00006004394,0.0019668038,0.9795136,0.00016756085,0.009586309,0.000020337617],"about_ca_topic_score_codex":0.00063654786,"about_ca_topic_score_gemma":0.00092086353,"teacher_disagreement_score":0.0015392137,"about_ca_system_score_codex":0.00031780466,"about_ca_system_score_gemma":0.00021638122,"threshold_uncertainty_score":0.005149126},"labels":[],"label_agreement":null},{"id":"W4415502906","doi":"10.1093/brain/awaf403","title":"Antisense oligonucleotides reverse SPTLC1-related hereditary sensory neuropathy in a mouse model","year":2025,"lang":"en","type":"article","venue":"Brain","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":0,"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":"Harrington Discovery Institute, University Hospitals; Medical Research Council; Centro Singular de Investigación de Galicia; Rosetrees Trust; National Institute for Health and Care Research; RTW Charitable Foundation; Medical Research Council Canada; University College London; INFRAFRONTIER","keywords":"Mutant; Gene silencing; Locked nucleic acid; Oligonucleotide; Wild type; Mutation; Peripheral neuropathy; Gene","score_opus":0.026267447880910767,"score_gpt":0.26262511107537817,"score_spread":0.2363576631944674,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4415502906","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":[0.96967006,0.0037871483,0.017205046,0.000542343,0.00054145773,0.0005365904,0.0017235675,0.0009651313,0.005028634],"genre_scores_gemma":[0.95281523,0.0055513117,0.016038323,0.00038796721,0.00009226848,0.0010644083,0.0024038015,0.00013274807,0.021514008],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99972135,0.000029279252,0.000027743998,0.00008998593,0.00008312945,0.00004840628],"domain_scores_gemma":[0.9998703,0.000015854104,0.000043295964,0.000012893058,0.00002453989,0.000033088072],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00020991653,0.0006322315,0.00040137256,0.00042413455,0.00017590048,0.0002475612,0.00037554582,0.00075450016,0.0019757168],"category_scores_gemma":[0.00009543166,0.00025230626,0.00036096544,0.0001879049,0.0002804443,0.000219793,0.00012909524,0.0014341829,0.0006450942],"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":[0.000084798114,0.00005619971,0.000034428616,0.000050731698,0.0000052616224,0.000041086518,0.000010776492,0.000046340254,0.99834037,0.00010431441,0.000102930615,0.0011226706],"study_design_scores_gemma":[0.00007642977,0.0015708603,0.00066747045,0.000013823254,0.000040278577,0.00035596537,0.000025231471,0.0007855114,0.991071,0.000057740108,0.0053279065,0.0000077076875],"about_ca_topic_score_codex":0.0007879066,"about_ca_topic_score_gemma":0.0014362527,"teacher_disagreement_score":0.0019757168,"about_ca_system_score_codex":0.0003166995,"about_ca_system_score_gemma":0.00038570163,"threshold_uncertainty_score":0.00660944},"labels":[],"label_agreement":null},{"id":"W4415641091","doi":"10.1186/s40035-025-00516-2","title":"Shared burden of ultra-rare genetic variants across a spectrum of motor neuron diseases","year":2025,"lang":"en","type":"letter","venue":"Translational Neurodegeneration","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":1,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":false,"ca_institutions":"University of British Columbia; Vancouver Coastal Health","funders":"National Center for Research Resources; National Institute of Neurological Disorders and Stroke; U.S. Food and Drug Administration; National Cancer Institute; National Institutes of Health; Rare Diseases Clinical Research Network; Target ALS; Wellcome Trust; ALS Association","keywords":"Genetic variants; Neurology; Motor neuron; Broad spectrum; Neuron; Genetic variation; Motor activity","score_opus":0.02782457630533288,"score_gpt":0.26004690104138783,"score_spread":0.23222232473605495,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4415641091","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":[0.37929475,0.022110563,0.00913266,0.5326471,0.008488352,0.00008058276,0.0014340786,0.00035080366,0.046461143],"genre_scores_gemma":[0.8659421,0.0073003327,0.0038624676,0.09102534,0.027211878,0.000048296908,0.00035924657,0.00007478688,0.004175449],"study_design_codex":"design_other","study_design_gemma":"observational","domain_scores_codex":[0.9993131,0.00017004934,0.00006152127,0.00018107907,0.0002077492,0.000066508495],"domain_scores_gemma":[0.99717784,0.0015429095,0.00034652502,0.0002797326,0.00037945146,0.00027360514],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00064052356,0.00018653499,0.0004934213,0.00041353918,0.0006568397,0.0006391119,0.00041223163,0.0024538063,0.0022876281],"category_scores_gemma":[0.004204689,0.00012716012,0.00017493471,0.00048504554,0.0008379311,0.0007470093,0.0006357991,0.0023076136,0.00092518784],"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":[0.0015375096,0.00016211724,0.2480681,0.0003689594,0.00028425318,0.16743056,0.0011179157,0.0011278738,0.020882292,0.016414866,0.26500398,0.27760163],"study_design_scores_gemma":[0.00024280307,0.0003493018,0.24142568,0.00063458586,0.00022551243,0.5022385,0.0014816197,0.004015507,0.0041686296,0.076667845,0.1684033,0.00014666341],"about_ca_topic_score_codex":0.0009528951,"about_ca_topic_score_gemma":0.0020995683,"teacher_disagreement_score":0.0024538063,"about_ca_system_score_codex":0.0005154049,"about_ca_system_score_gemma":0.00029244655,"threshold_uncertainty_score":0.0076528788},"labels":[],"label_agreement":null},{"id":"W4415976494","doi":"10.1101/2025.11.04.25339178","title":"Recessive genomic and phenotypic variation in consanguineous families with cerebral palsy","year":2025,"lang":"en","type":"preprint","venue":"medRxiv","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":false,"ca_institutions":"Artificial Intelligence in Medicine (Canada)","funders":"National Institutes of Health; Cerebral Palsy Alliance; Cerebral Palsy Alliance Research Foundation; Children's Discovery Institute","keywords":"Consanguinity; Phenotype; Mendelian inheritance; Gene; Multifactorial Inheritance; Allele; Genetic variation; Inheritance (genetic algorithm)","score_opus":0.022974739230735113,"score_gpt":0.25058986138759454,"score_spread":0.22761512215685942,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4415976494","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":[0.9992157,0.000088134635,0.00030530742,0.000013902486,0.0000028234783,0.0000027111466,0.0000866162,0.000007730553,0.00027703572],"genre_scores_gemma":[0.99959296,0.000052448962,0.00017510471,0.000008572116,0.0000025207955,0.0000020568623,0.000064757674,0.0000041917674,0.00009739038],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99974686,0.0000615055,0.00002181361,0.00009230771,0.00004697015,0.00003058657],"domain_scores_gemma":[0.99975914,0.000088238514,0.00006966375,0.000019937863,0.000017565895,0.0000454427],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0002425018,0.00058235606,0.0002223519,0.0009413854,0.0004777887,0.00035795005,0.00022155112,0.00026270552,0.0021035192],"category_scores_gemma":[0.0009502849,0.00020090779,0.0002116146,0.00055286265,0.0004255157,0.00009901204,0.0003891252,0.0002733094,0.00017662282],"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":[0.0012540513,0.00012377845,0.8262592,0.00006224487,0.0002975604,0.053806752,0.0016160073,0.00064716255,0.09820862,0.0007650452,0.0005786055,0.016380955],"study_design_scores_gemma":[0.000046663718,0.00028116393,0.9315499,0.00003666794,0.00018931204,0.05481461,0.0007294329,0.0019885385,0.008627814,0.00044660646,0.0012533992,0.00003582922],"about_ca_topic_score_codex":0.004419469,"about_ca_topic_score_gemma":0.003892694,"teacher_disagreement_score":0.004419469,"about_ca_system_score_codex":0.0001629771,"about_ca_system_score_gemma":0.000116576906,"threshold_uncertainty_score":0.008787513},"labels":[],"label_agreement":null},{"id":"W4415981210","doi":"","title":"GROSS MOTOR PERFORMANCE AND SENSORY PROCESSING RESULTS IN CHARCOT-MARIE TOOTH (TYPE 1C) DIAGNOSIS","year":2020,"lang":"tr","type":"article","venue":"","topic":"Hereditary Neurological Disorders","field":"Neuroscience","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":"Motor activity; Sensory system; Motor area; Motor system","score_opus":0.07434438172120109,"score_gpt":0.2689171463292278,"score_spread":0.19457276460802672,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4415981210","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":[0.9954332,0.00076652056,0.00022334086,0.00016530606,0.00001938844,0.00004220407,0.00045236622,0.000022046715,0.0028757136],"genre_scores_gemma":[0.9974408,0.0002632137,0.00025232375,0.00007554631,0.000011196108,0.000033208868,0.00049164856,0.0000074895847,0.0014245588],"study_design_codex":"observational","study_design_gemma":"case_report","domain_scores_codex":[0.99947256,0.00008157114,0.000065848544,0.00011676059,0.0001488332,0.0001143859],"domain_scores_gemma":[0.9988304,0.0002672781,0.00027334102,0.000048472855,0.00023672213,0.00034375826],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00054871244,0.0007621417,0.0005426658,0.0018050625,0.00069153786,0.00076194893,0.00042110658,0.0010596702,0.0036200683],"category_scores_gemma":[0.0025402966,0.00032788987,0.00069393736,0.0006866008,0.00065944425,0.0005051791,0.00079487433,0.0007268511,0.0006630158],"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":[0.001151871,0.0002984693,0.9697453,0.00008975667,0.00011746635,0.009453659,0.000641985,0.00043217803,0.0042062267,0.00009544293,0.00082033436,0.012947383],"study_design_scores_gemma":[0.00000909224,0.0002473313,0.9926252,0.00003196485,0.000028949444,0.0058753486,0.00025466803,0.00025175145,0.00035742935,0.00006808432,0.00023594241,0.00001424968],"about_ca_topic_score_codex":0.022566618,"about_ca_topic_score_gemma":0.018309323,"teacher_disagreement_score":0.022566618,"about_ca_system_score_codex":0.0010790166,"about_ca_system_score_gemma":0.0005626801,"threshold_uncertainty_score":0.044870555},"labels":[],"label_agreement":null},{"id":"W4416049142","doi":"10.18502/ijph.v54i10.20138","title":"Clinical and Genetic Variant Profile of Asian Charcot‐Marie Tooth Patients: A Systematic Review","year":2025,"lang":"en","type":"review","venue":"Iranian Journal of Public Health","topic":"Hereditary Neurological Disorders","field":"Neuroscience","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":"Genetic variants; MEDLINE; Cohort; Genetic testing; DNA sequencing; Genetic diagnosis; Mutation","score_opus":0.143849817730575,"score_gpt":0.3968719298697437,"score_spread":0.2530221121391687,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4416049142","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":[0.006763164,0.99096596,0.00011596064,0.00028775795,0.000072118986,0.00023876638,0.0011928919,0.0000070036663,0.00035643225],"genre_scores_gemma":[0.053979516,0.9435907,0.0005378404,0.0004749959,0.00006758777,0.00053641613,0.0006939764,0.000004603443,0.000114297894],"study_design_codex":"systematic_review","study_design_gemma":"systematic_review","domain_scores_codex":[0.9956867,0.0010009635,0.0021315217,0.00044940677,0.00056677294,0.00016454842],"domain_scores_gemma":[0.98552376,0.009173054,0.0033928882,0.00022419344,0.0014770649,0.00020896687],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0042687147,0.0010063641,0.00620377,0.010471344,0.0005070722,0.0017563995,0.0015396586,0.0013405317,0.0030580505],"category_scores_gemma":[0.016940687,0.0006802178,0.0043913648,0.01705493,0.00060532754,0.0014520136,0.0009495916,0.0004917969,0.00021299334],"study_design_candidate":"systematic_review","study_design_consensus":"systematic_review","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00019041395,0.00001655435,0.0063331076,0.95805174,0.010245618,0.00033854274,0.00038394585,0.000082448576,0.00018193529,0.000118495984,0.001426359,0.02263075],"study_design_scores_gemma":[0.00029876482,0.00030115285,0.03838133,0.7983739,0.14087622,0.0020622627,0.0011566568,0.00013655926,0.00024518577,0.00022051942,0.017876659,0.00007071944],"about_ca_topic_score_codex":0.0079269465,"about_ca_topic_score_gemma":0.022946952,"teacher_disagreement_score":0.010471344,"about_ca_system_score_codex":0.0019655256,"about_ca_system_score_gemma":0.007955648,"threshold_uncertainty_score":0.022575438},"labels":[],"label_agreement":null},{"id":"W4416257009","doi":"10.1212/wnl.0000000000214316","title":"Multiple System Atrophy Without Dysautonomia","year":2025,"lang":"en","type":"article","venue":"Neurology","topic":"Hereditary Neurological Disorders","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":"Ontario Brain Institute; Occupational Cancer Research Centre; Toronto Western Hospital; University Health Network","funders":"National Institute on Aging; Parkinsonfonden; National Institutes of Health; Canadian Institutes of Health Research; Parkinson Canada; Edmond J. Safra Philanthropic Foundation; Pfizer; Demensförbundet; University of Pennsylvania; Ludwig-Maximilians-Universität München; Bayer Vital; Fondation Brain Canada; Teva Pharmaceutical Industries; Bristol-Myers Squibb; Eli Lilly and Company; Biogen","keywords":"Dysautonomia; Natural history; Atrophy; Disease; Retrospective cohort study; Scope (computer science); Central nervous system disease","score_opus":0.017351802290457886,"score_gpt":0.24512358055331826,"score_spread":0.22777177826286038,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4416257009","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":[0.994293,0.0005829861,0.0004083688,0.000052292413,0.000013586061,0.000032236396,0.0003696926,0.00001597986,0.0042319265],"genre_scores_gemma":[0.9988593,0.00010970833,0.0002800317,0.00003629128,0.000013730835,0.000010973778,0.00024596116,0.0000035061562,0.00044056246],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9997085,0.000048705257,0.00004794805,0.000095292446,0.000053000364,0.000046533514],"domain_scores_gemma":[0.99911076,0.00017089091,0.0003710564,0.00006460224,0.0001452349,0.00013757398],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00028736432,0.0003030745,0.00040611852,0.00049407664,0.0005430238,0.00028109906,0.00018806657,0.0001477301,0.003988219],"category_scores_gemma":[0.0013603307,0.00007199669,0.0001164367,0.00039406703,0.00027644556,0.000282795,0.00027739472,0.0001953032,0.00040821216],"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":[0.0007017462,0.00014286263,0.9713712,0.00011438869,0.00009201168,0.0040748874,0.000201927,0.00008107181,0.0037108196,0.0003069473,0.00041209726,0.018790012],"study_design_scores_gemma":[0.000022341588,0.0006401568,0.9783996,0.000028627752,0.00004655814,0.018703619,0.000104175095,0.0001696851,0.0005741736,0.00029628878,0.0010107268,0.0000040237205],"about_ca_topic_score_codex":0.0014097422,"about_ca_topic_score_gemma":0.002867685,"teacher_disagreement_score":0.003988219,"about_ca_system_score_codex":0.00022115455,"about_ca_system_score_gemma":0.00037253788,"threshold_uncertainty_score":0.013341904},"labels":[],"label_agreement":null},{"id":"W4416328073","doi":"10.1212/nxi.0000000000200449","title":"Spinal Cord Leptomeningeal Enhancement as a Marker of Extensive Spinal Cord Involvement in Children With MOGAD","year":2025,"lang":"en","type":"article","venue":"Neurology Neuroimmunology & Neuroinflammation","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":1,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":false,"route_ca_venue":false,"route_about_ca":true,"ca_institutions":"SickKids Foundation; Ottawa Hospital; Montreal Neurological Institute and Hospital; Dalhousie University; University of Ottawa","funders":"","keywords":"Spinal cord; Cord; Central nervous system disease; Central nervous system; Lesion","score_opus":0.01927620104970906,"score_gpt":0.2810440360805897,"score_spread":0.26176783503088064,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4416328073","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":[0.9993783,0.0002190782,0.000027425875,0.000021616057,0.0000017603963,0.000006965943,0.00004807491,0.0000021683106,0.00029447235],"genre_scores_gemma":[0.99965096,0.00010117759,0.00013054987,0.000010313677,0.00000471382,0.000004820945,0.00005919979,9.421249e-7,0.000037275357],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9995552,0.00010630724,0.000044743683,0.000076203,0.00012999099,0.000087476976],"domain_scores_gemma":[0.99800533,0.00047366988,0.0009363734,0.000055031043,0.00019904149,0.00033046474],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0007153555,0.00033837502,0.0002514842,0.0009965716,0.0003212313,0.00045944558,0.00036095755,0.0005038903,0.0014990894],"category_scores_gemma":[0.0028535775,0.00021096572,0.00018874383,0.00059568917,0.0006043202,0.0005193061,0.0003986375,0.0004868474,0.00014347832],"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":[0.000053033946,0.000013418241,0.99824345,0.0000122433175,0.000007721469,0.00048339056,0.000082984414,0.000014778391,0.00043518658,0.000008214673,0.000030404368,0.0006152809],"study_design_scores_gemma":[0.0000031581592,0.000077424214,0.99686205,0.000011184725,0.000010405484,0.0026302878,0.00018869691,0.000047821108,0.00009308945,0.000007229774,0.00006689889,0.0000017985725],"about_ca_topic_score_codex":0.008938039,"about_ca_topic_score_gemma":0.014976539,"teacher_disagreement_score":0.008938039,"about_ca_system_score_codex":0.00043697938,"about_ca_system_score_gemma":0.0006185288,"threshold_uncertainty_score":0.017772019},"labels":[],"label_agreement":null},{"id":"W4416651770","doi":"10.1073/pnas.2517552122","title":"Drug repurposing screen identifies an HRI activating compound that promotes adaptive mitochondrial remodeling in MFN2-deficient cells","year":2025,"lang":"en","type":"article","venue":"Proceedings of the National Academy of Sciences","topic":"Hereditary Neurological Disorders","field":"Neuroscience","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":"Alberta Children's Hospital; University of Calgary","funders":"National Institute on Aging; Thailand Science Research and Innovation; Wellcome Trust; Canadian Institutes of Health Research; George E. Hewitt Foundation for Medical Research; National Science Foundation Graduate Research Fellowship Program; National Institute of Neurological Disorders and Stroke; American Heart Association; Bill and Melinda Gates Foundation; National Institutes of Health; National Science Foundation","keywords":"MFN2; Mitochondrion; mitochondrial fusion; DNAJA3; Signal transduction; Genetic screen; Drug repositioning; Mitochondrial respiratory chain; Mitochondrial DNA; Drug discovery","score_opus":0.09257607448108464,"score_gpt":0.3246552681740798,"score_spread":0.23207919369299518,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4416651770","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":[0.9868506,0.0022019672,0.0026053623,0.00032176543,0.000035146386,0.0002611889,0.0019922392,0.00028908384,0.005442658],"genre_scores_gemma":[0.9886723,0.0018912774,0.0030183871,0.00017496852,0.000009750336,0.00013476943,0.0023748665,0.00002253448,0.0037011548],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9999145,0.0000132168,0.0000099338495,0.000014302125,0.00003163342,0.000016501112],"domain_scores_gemma":[0.9999472,0.000009680378,0.000011193146,0.0000062975923,0.000009350761,0.00001633166],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0001413089,0.0005039657,0.00046509647,0.00038653793,0.00017010742,0.00025977794,0.0002553434,0.00037006967,0.0015603319],"category_scores_gemma":[0.000098013465,0.00011251817,0.00026506244,0.00020363035,0.00014070507,0.00011006259,0.00016982722,0.0003797484,0.0004504291],"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":[0.00021206537,0.00015575314,0.0003976831,0.000062448504,0.000015382853,0.00017975265,0.000010834736,0.00018818093,0.9928439,0.00007058246,0.00018688555,0.005676427],"study_design_scores_gemma":[0.00023711819,0.003394199,0.010074678,0.000013446425,0.000070245114,0.0010140751,0.000042474083,0.0012297243,0.978919,0.00004973325,0.0049417904,0.000013477289],"about_ca_topic_score_codex":0.00050335,"about_ca_topic_score_gemma":0.0020075983,"teacher_disagreement_score":0.0015603319,"about_ca_system_score_codex":0.00021290522,"about_ca_system_score_gemma":0.00025023494,"threshold_uncertainty_score":0.005219817},"labels":[],"label_agreement":null},{"id":"W4416705575","doi":"10.1055/s-0043-1777187","title":"Expanding SNX14-Associated Movement Disorders in a Genotype–Phenotype Spectrum","year":2023,"lang":"en","type":"article","venue":"Neuropediatrics","topic":"Hereditary Neurological Disorders","field":"Neuroscience","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":"Ottawa Hospital; Children's Hospital of Eastern Ontario; University of Ottawa","funders":"","keywords":"Movement disorders; Movement (music); Spectrum (functional analysis); MEDLINE","score_opus":0.028807613833048428,"score_gpt":0.2586116940227913,"score_spread":0.2298040801897429,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4416705575","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":[0.98506945,0.0013409066,0.0021781477,0.00057014613,0.000047877584,0.00005482804,0.00042443955,0.000065421744,0.010248782],"genre_scores_gemma":[0.995256,0.0009092296,0.0016528957,0.00024663444,0.0000990374,0.000019150924,0.00042116534,0.000043491036,0.0013524627],"study_design_codex":"case_report","study_design_gemma":"observational","domain_scores_codex":[0.9995128,0.000064691,0.00006317436,0.00013838163,0.0001369143,0.000084091975],"domain_scores_gemma":[0.9994066,0.00024955667,0.00010844171,0.000026023328,0.000103239334,0.00010616814],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00040689023,0.0021225186,0.0007273288,0.0024413979,0.00078205176,0.00061212917,0.0005561522,0.000991657,0.005269878],"category_scores_gemma":[0.0010678794,0.00026066517,0.0005273847,0.001080551,0.00097439607,0.0004895439,0.001312742,0.00046151635,0.00063471106],"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":[0.0014817191,0.00039116113,0.30126145,0.00025422193,0.00039475595,0.53223675,0.0015475166,0.0019052158,0.095256746,0.0051325867,0.003791631,0.056346174],"study_design_scores_gemma":[0.00010925368,0.000468628,0.3878624,0.00024862264,0.00041209953,0.5886521,0.0009169045,0.0021651858,0.008677212,0.004414349,0.0060174433,0.00005575775],"about_ca_topic_score_codex":0.0014899359,"about_ca_topic_score_gemma":0.00176957,"teacher_disagreement_score":0.005269878,"about_ca_system_score_codex":0.00026219583,"about_ca_system_score_gemma":0.00041250882,"threshold_uncertainty_score":0.017629504},"labels":[],"label_agreement":null},{"id":"W4416782592","doi":"10.1002/mds.70144","title":"Loss‐of‐Function Variants in <scp> <i>CPT1C</i> </scp> : No Support for a Causal Role in Hereditary Spastic Paraplegia","year":2025,"lang":"en","type":"article","venue":"Movement Disorders","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":0,"is_retracted":false,"has_abstract":true,"route_ca_aff":true,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":true,"ca_institutions":"University of Alberta; Université Laval; McMaster University; Montreal Neurological Institute and Hospital; University of Toronto; Children's Hospital of Eastern Ontario; McGill University; University of Ottawa","funders":"Amicus Therapeutics; Idorsia Pharmaceuticals; Canadian Institutes of Health Research; Alnylam Pharmaceuticals; McGill University; Campus France; Fonds de Recherche du Québec - Santé; Université de Bordeaux; Université Laval; Canada First Research Excellence Fund; Centre Hospitalier Universitaire de Québec; Agence Nationale de la Recherche","keywords":"Hereditary spastic paraplegia; Paraplegia; Movement disorders; Neurological disorder; Clinical neurology; Central nervous system disease; Spastic; Degenerative disease","score_opus":0.011880734129065852,"score_gpt":0.24084146347597762,"score_spread":0.22896072934691178,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4416782592","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":[0.9860292,0.0024948698,0.00069705583,0.0009205252,0.00007141609,0.000030338206,0.0038517243,0.000033930002,0.0058708983],"genre_scores_gemma":[0.9966287,0.00073949195,0.00027205946,0.00023453594,0.00004333136,0.0000069094667,0.0016567705,0.000013151915,0.00040505474],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99963915,0.000031351654,0.00003672801,0.00014083597,0.000093188144,0.000058712805],"domain_scores_gemma":[0.99812645,0.0006944391,0.00049643236,0.00012296425,0.00035093172,0.0002088332],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.000604205,0.0004200137,0.00030071725,0.0007766452,0.00051559485,0.00059963757,0.0006525388,0.00038869088,0.0062525133],"category_scores_gemma":[0.00352965,0.00009031493,0.0002634952,0.0007350361,0.0010504354,0.00026566736,0.00033851233,0.00035366495,0.00048210402],"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":[0.0018128103,0.00003785369,0.9654028,0.00034766874,0.0004280483,0.0033928305,0.00034425393,0.0003960805,0.007251376,0.00071689015,0.0036910137,0.016178448],"study_design_scores_gemma":[0.000116875024,0.00015048467,0.9827891,0.00035402068,0.0005899546,0.005815043,0.00048790948,0.0013906314,0.0019999547,0.0008039597,0.0054809735,0.000021072714],"about_ca_topic_score_codex":0.07390685,"about_ca_topic_score_gemma":0.07482084,"teacher_disagreement_score":0.07390685,"about_ca_system_score_codex":0.0010190979,"about_ca_system_score_gemma":0.0015819148,"threshold_uncertainty_score":0.14695328},"labels":[],"label_agreement":null},{"id":"W4417167179","doi":"10.3390/osteology5040036","title":"Outcomes of Primary Fusion vs. Reconstruction of Pediatric Cavus Foot in Charcot-Marie-Tooth Disease: A Systematic Review","year":2025,"lang":"en","type":"article","venue":"Osteology","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":false,"ca_institutions":"Western University; University of Toronto; McMaster University","funders":"","keywords":"Pes cavus; Deformity; Radiography; Arthrodesis; Psychological intervention; Foot (prosody)","score_opus":0.018793946344233526,"score_gpt":0.25869243966866573,"score_spread":0.2398984933244322,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4417167179","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":[0.0034670285,0.99513716,0.00009864769,0.00013994455,0.000065781314,0.00029004374,0.0005531009,0.000007937538,0.00024038316],"genre_scores_gemma":[0.051969063,0.94546074,0.0005094787,0.00050994207,0.00009586794,0.0008171132,0.00047708812,0.000008799573,0.00015177837],"study_design_codex":"systematic_review","study_design_gemma":"systematic_review","domain_scores_codex":[0.99453944,0.0015978793,0.0024411327,0.00047897472,0.00073076267,0.00021178043],"domain_scores_gemma":[0.97695106,0.016049474,0.0049200878,0.00024170012,0.0015730585,0.00026466243],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.005712287,0.0013216779,0.0095769465,0.007836634,0.0006058664,0.0027511548,0.0018010151,0.0018412434,0.0040958873],"category_scores_gemma":[0.026740931,0.0008961803,0.008871011,0.008478703,0.0008238476,0.002124868,0.0014293172,0.00096501777,0.00024114587],"study_design_candidate":"systematic_review","study_design_consensus":"systematic_review","about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00039407116,0.000011916839,0.0010731464,0.97388804,0.012113627,0.00007310574,0.00013019302,0.00005742131,0.000102829705,0.00008111306,0.00047889995,0.011595621],"study_design_scores_gemma":[0.0005382475,0.0004308533,0.006702705,0.8209171,0.16206802,0.00049805734,0.00039737346,0.000110813904,0.00020304119,0.00021244348,0.0078775715,0.00004380859],"about_ca_topic_score_codex":0.006550026,"about_ca_topic_score_gemma":0.018042281,"teacher_disagreement_score":0.0095769465,"about_ca_system_score_codex":0.0033166113,"about_ca_system_score_gemma":0.0072785164,"threshold_uncertainty_score":0.03020984},"labels":[],"label_agreement":null},{"id":"W4417180070","doi":"10.1002/mds.70142","title":"Longitudinal Dynamics of Plasma Neurofilament Light Chain in Hereditary Spastic Paraplegia Type 11 ( <scp>HSP</scp> ‐ <scp> <i>SPG11</i> </scp> ) and Type 15 ( <scp>HSP</scp> ‐ <scp> <i>ZFYVE26</i> </scp> )","year":2025,"lang":"en","type":"article","venue":"Movement Disorders","topic":"Hereditary Neurological Disorders","field":"Neuroscience","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":"Hospital for Sick Children","funders":"National Institute of Neurological Disorders and Stroke; Spastic Paraplegia Foundation","keywords":"Hereditary spastic paraplegia; Paraplegia; Degenerative disease; Spasticity; Central nervous system disease; Spastic; Neurological disorder","score_opus":0.014753771902694585,"score_gpt":0.23592227331442,"score_spread":0.22116850141172542,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4417180070","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":[0.99942845,0.0001566163,0.00010009143,0.000009248513,0.0000016753003,0.00000251192,0.00017950017,0.000005516901,0.00011629704],"genre_scores_gemma":[0.9994185,0.0000461231,0.000092388604,0.000010014003,0.0000031364812,0.0000058976393,0.00028058342,0.0000013034062,0.00014202809],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99981314,0.000029124005,0.000016566228,0.00008073885,0.000030257843,0.000030227156],"domain_scores_gemma":[0.99917823,0.0001321302,0.00041059774,0.000036583337,0.00010050958,0.0001419574],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00038010784,0.00018623554,0.00021495965,0.00045651992,0.0002001449,0.00033558425,0.00014284573,0.00041648973,0.0010148557],"category_scores_gemma":[0.0010449099,0.00012855056,0.00016502831,0.0003470173,0.00017353009,0.00026001755,0.00024039269,0.00032129226,0.00022872508],"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":[0.001431505,0.00006960393,0.9812921,0.000019281622,0.00010020461,0.0002959102,0.00013115018,0.00015332937,0.010743428,0.000023131064,0.00013935204,0.0056011304],"study_design_scores_gemma":[0.0000069302673,0.00026999114,0.9981324,0.000002682807,0.000027754848,0.00048596715,0.000047410485,0.00019649975,0.000720451,0.000015309319,0.0000914126,0.000003317121],"about_ca_topic_score_codex":0.0012197864,"about_ca_topic_score_gemma":0.0010556937,"teacher_disagreement_score":0.0012197864,"about_ca_system_score_codex":0.0002540854,"about_ca_system_score_gemma":0.00010292668,"threshold_uncertainty_score":0.003395021},"labels":[],"label_agreement":null},{"id":"W4417424343","doi":"10.1017/cjn.2025.10478","title":"Exploring Clinico-Genetic Heterogeneity with Two Novel Mutations in KIF1A Gene","year":2025,"lang":"en","type":"article","venue":"Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques","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":true,"route_about_ca":false,"ca_institutions":"London Health Sciences Centre; Western University","funders":"","keywords":"Gene; Mutation; Sequence (biology); Genome; Identification (biology)","score_opus":0.15296096320175054,"score_gpt":0.3227616086845864,"score_spread":0.16980064548283588,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4417424343","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":[0.9936342,0.00047626934,0.00094675564,0.0005277765,0.000047470287,0.00005659364,0.00038527153,0.000053311946,0.0038723343],"genre_scores_gemma":[0.9984724,0.00014079185,0.0005018867,0.000089256646,0.0000343886,0.000008343274,0.00012560272,0.00001039109,0.0006169448],"study_design_codex":"case_report","study_design_gemma":"observational","domain_scores_codex":[0.9996518,0.000025210633,0.000037523776,0.00012786897,0.000060163304,0.00009740838],"domain_scores_gemma":[0.9993938,0.0002451046,0.00011199062,0.000031092473,0.000053249627,0.00016477655],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00024011779,0.0008743043,0.0003633117,0.0025210571,0.0007465396,0.0006689382,0.000681114,0.001770453,0.0040159635],"category_scores_gemma":[0.0015103503,0.00031690093,0.00046878678,0.0009985109,0.00089950894,0.00043462927,0.0006892367,0.00068691437,0.0005325163],"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":[0.00052708364,0.00019499121,0.06462623,0.00007592477,0.00006983553,0.88832474,0.00087346754,0.00038577826,0.03554283,0.0010669283,0.0010235735,0.007288583],"study_design_scores_gemma":[0.000070538124,0.00024255914,0.09321158,0.000037899626,0.00012342715,0.89377487,0.00059935736,0.0013955717,0.0073351893,0.00074618193,0.0024172054,0.00004558507],"about_ca_topic_score_codex":0.004217196,"about_ca_topic_score_gemma":0.0033565657,"teacher_disagreement_score":0.004217196,"about_ca_system_score_codex":0.0005666283,"about_ca_system_score_gemma":0.00035174814,"threshold_uncertainty_score":0.013434708},"labels":[],"label_agreement":null},{"id":"W4417535393","doi":"10.1002/mus.70122","title":"Relationships Between Nerve Ultrasound Findings and Clinical, Genetic, Laboratory and Electrophysiological Findings in Patients With Chronic Idiopathic Axonal Polyneuropathy","year":2025,"lang":"en","type":"article","venue":"Muscle & Nerve","topic":"Hereditary Neurological Disorders","field":"Neuroscience","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":"Electrophysiology; Polyneuropathy; Ultrasound; Sensory system; Axonal degeneration; Sensory nerve; Electrodiagnosis; Median nerve","score_opus":0.02236771039348618,"score_gpt":0.2540870177185732,"score_spread":0.23171930732508705,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W4417535393","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":[0.9996711,0.00009193868,0.000026458572,0.000013224247,0.000001769447,0.0000035136404,0.00003168667,9.708509e-7,0.00015935424],"genre_scores_gemma":[0.9997967,0.000027266604,0.00005639678,0.000014331253,0.000007140812,0.0000049420946,0.000057990066,5.56695e-7,0.000034694058],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99944407,0.0001266593,0.000096118325,0.0001245238,0.00010374025,0.00010477808],"domain_scores_gemma":[0.9967533,0.001230086,0.0010943585,0.000090139096,0.00031547897,0.0005166707],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00065817067,0.00039645142,0.0002776347,0.0009232989,0.00060138264,0.0005793168,0.00027461775,0.000658133,0.0031718623],"category_scores_gemma":[0.004113737,0.00022523888,0.00018474915,0.00061281765,0.00054603675,0.0005280904,0.0004600311,0.00040471385,0.00025993277],"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":[0.000073318864,0.000015269723,0.99884605,0.0000042960705,0.000007527545,0.00035059947,0.00003806447,0.000016963244,0.00022527315,0.0000040341147,0.000015005659,0.00040352845],"study_design_scores_gemma":[0.000011841092,0.00033912665,0.9931631,0.0000097839165,0.000016013755,0.0058433665,0.00027937585,0.00015474723,0.00009374398,0.000018443887,0.00006592537,0.0000044699555],"about_ca_topic_score_codex":0.0014053656,"about_ca_topic_score_gemma":0.0018569113,"teacher_disagreement_score":0.0031718623,"about_ca_system_score_codex":0.0002951439,"about_ca_system_score_gemma":0.00031172624,"threshold_uncertainty_score":0.010610938},"labels":[],"label_agreement":null},{"id":"W6902079429","doi":"10.6084/m9.figshare.21275690.v1","title":"Additional file 1 of Evaluation of children with severe neurological impairment admitted to hospital with pain and irritability","year":2022,"lang":"en","type":"article","venue":"Figshare","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":false,"ca_institutions":"BC Children's Hospital; Children's Hospital of Eastern Ontario; University of British Columbia; University of Ottawa","funders":"","keywords":"Irritability; Medical diagnosis; Table (database); Hospital admission; Diagnosis code","score_opus":0.02493822708619312,"score_gpt":0.23212328284037742,"score_spread":0.2071850557541843,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W6902079429","genre_codex":"dataset","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":[0.000728345,0.000016533328,0.0000934179,0.00014014238,0.00001926218,0.00015467894,0.9958674,0.00005414632,0.00292613],"genre_scores_gemma":[0.019512787,0.00020941456,0.0012484513,0.0008409965,0.0001515627,0.0031391045,0.9575382,0.00022954638,0.017129907],"study_design_codex":"not_applicable","study_design_gemma":"observational","domain_scores_codex":[0.9994456,0.00010308566,0.0001304072,0.00013685743,0.00008585017,0.00009807483],"domain_scores_gemma":[0.9910336,0.004678528,0.0015496834,0.0005348884,0.0017497543,0.00045356483],"candidate_categories":["insufficient_payload"],"consensus_categories":[],"category_scores_codex":[0.0006487527,0.0007298736,0.00078047195,0.0015578275,0.00096160674,0.0007302337,0.0009189405,0.00082514866,0.7544396],"category_scores_gemma":[0.014450861,0.00031980153,0.00047197472,0.0025311173,0.00013352056,0.0009741571,0.0007135607,0.0006615492,0.074619845],"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":[0.0003689057,0.00010201741,0.008349913,0.0008430543,0.000028224555,0.00013950976,0.000081508144,0.00016092797,0.000049272963,0.00047527527,0.98225766,0.007143827],"study_design_scores_gemma":[0.0055766082,0.0005292952,0.2119671,0.0074057267,0.0001920097,0.0018243608,0.0014144136,0.0016546691,0.0008707453,0.007836465,0.76055944,0.00016921187],"about_ca_topic_score_codex":0.014192592,"about_ca_topic_score_gemma":0.020792425,"teacher_disagreement_score":0.7544396,"about_ca_system_score_codex":0.0011610377,"about_ca_system_score_gemma":0.0014890204,"threshold_uncertainty_score":0.3502621},"labels":[],"label_agreement":null},{"id":"W6902127902","doi":"10.6084/m9.figshare.15153901.v1","title":"Additional file 6 of Childhood-onset dystonia-causing KMT2B variants result in a distinctive genomic hypermethylation profile","year":2021,"lang":"en","type":"article","venue":"Figshare","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":false,"ca_institutions":"London Health Sciences Centre; Western University","funders":"","keywords":"Missense mutation; Classifier (UML); Genome; DNA methylation; DNA sequencing; Cluster analysis","score_opus":0.041604009558003044,"score_gpt":0.24789014973664963,"score_spread":0.2062861401786466,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W6902127902","genre_codex":"dataset","genre_gemma":"other","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"other","genre_consensus":null,"domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.000289688,0.000021021804,0.00022001803,0.00009921927,0.000020830219,0.000050364284,0.99835014,0.00030270143,0.0006459619],"genre_scores_gemma":[0.012707258,0.00016943325,0.0036563794,0.00057285465,0.00009851938,0.001103463,0.9715845,0.0008838639,0.009223811],"study_design_codex":"not_applicable","study_design_gemma":"not_applicable","domain_scores_codex":[0.99944025,0.000074074225,0.00010626228,0.00017533745,0.00011663062,0.00008737362],"domain_scores_gemma":[0.9871525,0.009789245,0.00078944815,0.0007554564,0.0011502702,0.00036293338],"candidate_categories":["insufficient_payload"],"consensus_categories":[],"category_scores_codex":[0.0011613584,0.001069679,0.0012660128,0.0018052299,0.00084918004,0.0014900331,0.0017575165,0.0012650494,0.86614615],"category_scores_gemma":[0.019439489,0.00050317514,0.000919205,0.0023008075,0.00023210915,0.0013184644,0.0008942475,0.0007375126,0.14987692],"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":[0.0005304595,0.000114671784,0.0064200056,0.0032100917,0.00008488234,0.00026124914,0.00009715135,0.0004113857,0.00028393668,0.00052537257,0.9749014,0.013159403],"study_design_scores_gemma":[0.007870201,0.00048042106,0.08547156,0.005613168,0.0003862059,0.0026519052,0.000742295,0.0036108305,0.002602889,0.013400353,0.8768632,0.00030700737],"about_ca_topic_score_codex":0.0076331566,"about_ca_topic_score_gemma":0.0146752,"teacher_disagreement_score":0.86614615,"about_ca_system_score_codex":0.00085079344,"about_ca_system_score_gemma":0.0013119908,"threshold_uncertainty_score":0.19092631},"labels":[],"label_agreement":null},{"id":"W6920576331","doi":"10.60692/rsdee-c4z68","title":"Identification and characterization of miRNAs and targets in flax (Linum usitatissimum) under saline, alkaline, and saline-alkaline stresses","year":2016,"lang":"en","type":"article","venue":"Greater South Information System","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":false,"ca_institutions":"Alberta Innovates","funders":"","keywords":"Transcriptome; WRKY protein domain; microRNA; Gene; Gene expression; Gene expression profiling; Linum; Deep sequencing; Transcription factor","score_opus":0.03181422343095544,"score_gpt":0.22978362406120748,"score_spread":0.19796940063025203,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W6920576331","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":[0.9914152,0.0016460178,0.003837996,0.00006687146,0.000013498971,0.000041347368,0.0020311393,0.00008979395,0.00085811847],"genre_scores_gemma":[0.97664136,0.0014530299,0.009570637,0.00024378927,0.000027019534,0.00020705289,0.007644048,0.000087472436,0.0041256077],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9999143,0.0000063341986,0.00000700149,0.00003773555,0.000019657693,0.00001492949],"domain_scores_gemma":[0.99989986,0.000017873372,0.00003243157,0.0000055074834,0.000026482097,0.000017805218],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00013196256,0.00037793812,0.00042747534,0.00036698752,0.0003224826,0.00027726436,0.0000936619,0.0002795239,0.00040930792],"category_scores_gemma":[0.00015796874,0.00018075455,0.00035464525,0.00026961358,0.00014216902,0.00025718537,0.00019122462,0.0003007898,0.00027445625],"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":[0.00009274832,0.0000070741753,0.0009127004,0.000047529542,0.0000047454155,0.000051736162,0.000043325486,0.0000558141,0.99699926,0.000024305042,0.0000319428,0.0017288357],"study_design_scores_gemma":[0.000038322916,0.00068050437,0.23929319,0.000041720345,0.0001508548,0.0014212731,0.0003373879,0.0039164135,0.74120164,0.00025329116,0.012606452,0.000058977304],"about_ca_topic_score_codex":0.0008694995,"about_ca_topic_score_gemma":0.0011496553,"teacher_disagreement_score":0.0008694995,"about_ca_system_score_codex":0.0001518622,"about_ca_system_score_gemma":0.0001853464,"threshold_uncertainty_score":0.0017288923},"labels":[],"label_agreement":null},{"id":"W6929404097","doi":"10.48550/arxiv.0812.4441","title":"Dynamical and thermal evolution of the quark-nova ejecta","year":2008,"lang":"en","type":"preprint","venue":"arXiv (Cornell University)","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":false,"ca_institutions":"University of Calgary","funders":"","keywords":"Ejecta; Breakup; Thermal; Break-Up; Neutron star; Crust; Stellar evolution; Gravitational collapse","score_opus":0.08358570988932776,"score_gpt":0.18515441399773588,"score_spread":0.10156870410840813,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W6929404097","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":[0.9944173,0.00013981624,0.0016991912,0.000059458238,0.0000053104786,0.000006754314,0.00011384663,0.000031171257,0.0035271072],"genre_scores_gemma":[0.9978963,0.00010488004,0.00085198315,0.00001347986,0.000004403818,0.000004971749,0.00018785844,0.000025791656,0.0009102517],"study_design_codex":"simulation_or_modeling","study_design_gemma":"simulation_or_modeling","domain_scores_codex":[0.9999424,0.000009613301,0.0000022213455,0.000013039112,0.000011200354,0.00002141601],"domain_scores_gemma":[0.9998498,0.000029294915,0.00003783423,0.000008438826,0.000015874793,0.00005876198],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00018450235,0.0003027294,0.00026230534,0.00043604602,0.0004985848,0.0007319961,0.00029435454,0.00042743742,0.001402855],"category_scores_gemma":[0.0007585147,0.00027644634,0.00040960708,0.00028032,0.00052403635,0.00053437235,0.0008903463,0.00042730727,0.0002485543],"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":[0.0015455371,0.00041107455,0.28965792,0.00015810927,0.0004083895,0.007653861,0.0019755866,0.4024221,0.2335841,0.04029327,0.0015349948,0.020355046],"study_design_scores_gemma":[0.00013282958,0.0002888558,0.3596437,0.00003497116,0.00007725804,0.0015284248,0.0007572246,0.60586095,0.01729069,0.011191265,0.003042479,0.00015128194],"about_ca_topic_score_codex":0.005377162,"about_ca_topic_score_gemma":0.0038881183,"teacher_disagreement_score":0.005377162,"about_ca_system_score_codex":0.0008502351,"about_ca_system_score_gemma":0.00022719929,"threshold_uncertainty_score":0.010691762},"labels":[],"label_agreement":null},{"id":"W6929522244","doi":"10.48550/arxiv.astro-ph/0401395","title":"Molecular Gas in Candidate Double Barred Galaxies III. A Lack of Molecular Gas?","year":2004,"lang":"en","type":"preprint","venue":"arXiv (Cornell University)","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":false,"ca_institutions":"McMaster University","funders":"","keywords":"Galaxy; Peculiar galaxy; Luminous infrared galaxy; Galaxy group; Radio galaxy; Disc; Solar mass","score_opus":0.08658577423868001,"score_gpt":0.21793776898731856,"score_spread":0.13135199474863857,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W6929522244","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":[0.997835,0.0005602542,0.00088136666,0.00007350257,0.0000041161215,0.00000472763,0.000034071898,0.000024488954,0.000582543],"genre_scores_gemma":[0.99911124,0.00009726208,0.0005431927,0.000016100448,0.0000028958827,0.000002373641,0.000037679438,0.0000022693137,0.00018703807],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.99992406,0.000008067718,0.000004170754,0.0000248539,0.000015841657,0.000022960443],"domain_scores_gemma":[0.9998017,0.000033309858,0.0000712685,0.000020592128,0.000016602098,0.000056625733],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00020822708,0.0003118752,0.0003457341,0.000812492,0.00025770426,0.0008131868,0.0006112908,0.0006867746,0.0013926963],"category_scores_gemma":[0.00054304453,0.00020470023,0.00020238999,0.00031631114,0.00071065413,0.00071868114,0.00044825877,0.00020333253,0.00023706003],"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":[0.0010290891,0.00012583923,0.82865655,0.00022946036,0.00009943905,0.005042987,0.00081036467,0.0043739122,0.1288815,0.007444928,0.0003922745,0.02291369],"study_design_scores_gemma":[0.00011105596,0.0005968628,0.85646045,0.00014438448,0.00020201459,0.013578207,0.002125011,0.05156361,0.04975316,0.020880446,0.004518108,0.00006667143],"about_ca_topic_score_codex":0.0016166731,"about_ca_topic_score_gemma":0.0023871276,"teacher_disagreement_score":0.0016166731,"about_ca_system_score_codex":0.00033797862,"about_ca_system_score_gemma":0.00009762096,"threshold_uncertainty_score":0.004658997},"labels":[],"label_agreement":null},{"id":"W6931009613","doi":"10.5281/zenodo.3796924","title":"Rhamphomyia (Pararhamphomyia) petervajdai Sinclair, Vajda, Saigusa & Shamshev 2019, sp. nov.","year":2019,"lang":"en","type":"article","venue":"Zenodo (CERN European Organization for Nuclear Research)","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":"McGill University; Canadian Food Inspection Agency","funders":"","keywords":"Field (mathematics); Holotype; Paraphernalia; Third party","score_opus":0.04191381449267867,"score_gpt":0.2442195351914655,"score_spread":0.20230572069878683,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W6931009613","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":[0.24593449,0.056069344,0.007608059,0.0025385264,0.005975676,0.0027109976,0.03470848,0.0019483169,0.6425061],"genre_scores_gemma":[0.73157936,0.04146792,0.021211315,0.0027084316,0.001039927,0.0019108469,0.023680815,0.000366007,0.17603537],"study_design_codex":"design_other","study_design_gemma":"not_applicable","domain_scores_codex":[0.9997037,0.00001902651,0.0000323729,0.00008286205,0.00009820641,0.00006370509],"domain_scores_gemma":[0.9997663,0.000035519486,0.000074335076,0.000032023694,0.000058742957,0.000033099335],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0002348045,0.0013903924,0.00061458524,0.0017252612,0.0032577994,0.0009696698,0.0010392952,0.0011870351,0.020835917],"category_scores_gemma":[0.00077006716,0.00047952618,0.00028018132,0.0020025193,0.00081583776,0.0015015054,0.0009780136,0.0016741968,0.012788381],"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":[0.00043346974,0.00014977765,0.024987692,0.00172481,0.00022690758,0.0027206677,0.0031355724,0.001128077,0.01450345,0.0028295731,0.09992999,0.84822994],"study_design_scores_gemma":[0.00018938749,0.00026678236,0.20842189,0.0018711905,0.00032691783,0.007351507,0.004357967,0.0006904741,0.0028708007,0.0009642858,0.772592,0.00009675411],"about_ca_topic_score_codex":0.116224185,"about_ca_topic_score_gemma":0.22671425,"teacher_disagreement_score":0.116224185,"about_ca_system_score_codex":0.0017942837,"about_ca_system_score_gemma":0.0020142205,"threshold_uncertainty_score":0.23109531},"labels":[],"label_agreement":null},{"id":"W6939780077","doi":"10.6084/m9.figshare.19418218","title":"Additional file 1 of An integrated modelling methodology for estimating global incidence and prevalence of hereditary spastic paraplegia subtypes SPG4, SPG7, SPG11, and SPG15","year":2022,"lang":"en","type":"article","venue":"Open MIND","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":false,"ca_institutions":"University of Toronto","funders":"","keywords":"Incidence (geometry); Hereditary spastic paraplegia; Paraplegia; Disease; MEDLINE","score_opus":0.13869902707725468,"score_gpt":0.3454145450606453,"score_spread":0.2067155179833906,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W6939780077","genre_codex":"dataset","genre_gemma":"methods","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"methods","genre_consensus":null,"domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.00092810544,0.00002203999,0.005671412,0.00015031394,0.00001862631,0.00013271067,0.99110436,0.00044708708,0.0015254206],"genre_scores_gemma":[0.07097285,0.00021167813,0.049861223,0.0005818899,0.00009234349,0.005636765,0.85597855,0.0015460843,0.0151186455],"study_design_codex":"not_applicable","study_design_gemma":"simulation_or_modeling","domain_scores_codex":[0.9991291,0.00039222933,0.000101530044,0.0002015972,0.00011026186,0.000065360335],"domain_scores_gemma":[0.9760399,0.02092697,0.0007724586,0.0009253442,0.0011690783,0.00016624224],"candidate_categories":["insufficient_payload"],"consensus_categories":[],"category_scores_codex":[0.003195258,0.00075765746,0.0006374831,0.001252632,0.0004299247,0.0009619307,0.0015327769,0.0010275998,0.6015145],"category_scores_gemma":[0.03595752,0.00049536,0.0010564931,0.0024659717,0.00017699355,0.0007816789,0.0006695192,0.00097375613,0.05100543],"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":[0.00035268845,0.00013203762,0.021415902,0.001625134,0.00029409264,0.00015108896,0.00021637663,0.01376077,0.00012579178,0.0051756287,0.9287484,0.028002087],"study_design_scores_gemma":[0.0047322093,0.0006009711,0.070521146,0.0031412663,0.0011708227,0.0011172867,0.0011087679,0.08573839,0.0014198862,0.050434183,0.77977663,0.00023835161],"about_ca_topic_score_codex":0.01960813,"about_ca_topic_score_gemma":0.020550352,"teacher_disagreement_score":0.6015145,"about_ca_system_score_codex":0.00087830896,"about_ca_system_score_gemma":0.0014779563,"threshold_uncertainty_score":0.5683912},"labels":[],"label_agreement":null},{"id":"W6945422376","doi":"10.25593/open-fau-1840","title":"Mobile digitale Ganganalyse zur objektiven longitudinalen Erfassung der Krankheitsprogression der Hereditären Spastischen Paraplegie","year":2025,"lang":"de","type":"article","venue":"","topic":"Hereditary Neurological Disorders","field":"Neuroscience","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":"Statistical analysis; Palliative care","score_opus":0.024495930873781577,"score_gpt":0.3060616826841205,"score_spread":0.2815657518103389,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W6945422376","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":[0.71002585,0.037892297,0.11192472,0.0065082004,0.0026167084,0.007981385,0.08914548,0.0035477644,0.030357644],"genre_scores_gemma":[0.8543144,0.009180496,0.0782977,0.002353304,0.0012329438,0.020559963,0.021641035,0.00037752662,0.0120426845],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9960873,0.0019101213,0.00052481866,0.00072724564,0.0005267879,0.00022371045],"domain_scores_gemma":[0.9880927,0.0045010247,0.0021962347,0.0011707637,0.0035063191,0.00053286954],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0060276994,0.001031934,0.00134214,0.002695898,0.000641072,0.002238229,0.0010886078,0.0010810167,0.016253686],"category_scores_gemma":[0.021003615,0.0005470995,0.0017658746,0.002359717,0.00038771372,0.0016044658,0.0016536572,0.0012183394,0.0026621076],"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":[0.010157185,0.0014427422,0.5041595,0.00817351,0.0050850697,0.0007979319,0.0027150898,0.003404576,0.005572224,0.00405415,0.043155923,0.411282],"study_design_scores_gemma":[0.001973146,0.0077732494,0.8362181,0.0052825757,0.0052115107,0.0028049462,0.00223039,0.0159111,0.009996558,0.011916889,0.100209266,0.00047224015],"about_ca_topic_score_codex":0.001701223,"about_ca_topic_score_gemma":0.0031596993,"teacher_disagreement_score":0.016253686,"about_ca_system_score_codex":0.000539612,"about_ca_system_score_gemma":0.0013270089,"threshold_uncertainty_score":0.05437398},"labels":[],"label_agreement":null},{"id":"W6957992795","doi":"10.6084/m9.figshare.15153895","title":"Additional file 4 of Childhood-onset dystonia-causing KMT2B variants result in a distinctive genomic hypermethylation profile","year":2021,"lang":"en","type":"article","venue":"Figshare","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":false,"ca_institutions":"London Health Sciences Centre; Western University","funders":"","keywords":"Selection (genetic algorithm); Genome; Cluster (spacecraft); Sample (material); genomic DNA; Genomics","score_opus":0.04194155674570194,"score_gpt":0.24819021338517697,"score_spread":0.20624865663947503,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W6957992795","genre_codex":"dataset","genre_gemma":"dataset","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"dataset","genre_consensus":"dataset","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.00047561343,0.00002702893,0.0005105744,0.000103126964,0.00003178966,0.00005898725,0.99757355,0.00058473094,0.0006345511],"genre_scores_gemma":[0.014542544,0.00014703319,0.0058305496,0.0006019909,0.00009187467,0.0012620371,0.9679002,0.001401859,0.008221934],"study_design_codex":"not_applicable","study_design_gemma":"not_applicable","domain_scores_codex":[0.99928135,0.00009750163,0.00011553941,0.00023412144,0.00016019931,0.00011123064],"domain_scores_gemma":[0.98440695,0.012201493,0.0007328751,0.001008977,0.0012546865,0.00039501349],"candidate_categories":["insufficient_payload"],"consensus_categories":[],"category_scores_codex":[0.0014385224,0.0012332974,0.001380592,0.0020192752,0.0011244403,0.0015335403,0.0019596554,0.0014079462,0.8367712],"category_scores_gemma":[0.02084108,0.00058570266,0.0010469711,0.0023068748,0.00030625885,0.0012386363,0.0009304331,0.0009368097,0.1266462],"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":[0.0008338876,0.00016761862,0.008020088,0.0038443792,0.00013377494,0.00039730512,0.00014951765,0.0007311896,0.0008726728,0.0005863927,0.9683092,0.015954033],"study_design_scores_gemma":[0.009535125,0.0006432852,0.09801222,0.004579886,0.00063208473,0.0031886136,0.00087833015,0.005103351,0.0059058596,0.014018219,0.85713446,0.00036855694],"about_ca_topic_score_codex":0.006874578,"about_ca_topic_score_gemma":0.014298618,"teacher_disagreement_score":0.8367712,"about_ca_system_score_codex":0.00089797575,"about_ca_system_score_gemma":0.0015507347,"threshold_uncertainty_score":0.23282611},"labels":[],"label_agreement":null},{"id":"W6958142189","doi":"10.6084/m9.figshare.15153901","title":"Additional file 6 of Childhood-onset dystonia-causing KMT2B variants result in a distinctive genomic hypermethylation profile","year":2021,"lang":"en","type":"article","venue":"Figshare","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":false,"ca_institutions":"London Health Sciences Centre; Western University","funders":"","keywords":"Missense mutation; Classifier (UML); Genome; DNA methylation; DNA sequencing; Cluster analysis","score_opus":0.041604009558003044,"score_gpt":0.24789014973664963,"score_spread":0.2062861401786466,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W6958142189","genre_codex":"dataset","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":[0.000289688,0.000021021804,0.00022001803,0.00009921927,0.000020830219,0.000050364284,0.99835014,0.00030270143,0.0006459619],"genre_scores_gemma":[0.012707258,0.00016943325,0.0036563794,0.00057285465,0.00009851938,0.001103463,0.9715845,0.0008838639,0.009223811],"study_design_codex":"not_applicable","study_design_gemma":"observational","domain_scores_codex":[0.99944025,0.000074074225,0.00010626228,0.00017533745,0.00011663062,0.00008737362],"domain_scores_gemma":[0.9871525,0.009789245,0.00078944815,0.0007554564,0.0011502702,0.00036293338],"candidate_categories":["insufficient_payload"],"consensus_categories":[],"category_scores_codex":[0.0011613584,0.001069679,0.0012660128,0.0018052299,0.00084918004,0.0014900331,0.0017575165,0.0012650494,0.86614615],"category_scores_gemma":[0.019439489,0.00050317514,0.000919205,0.0023008075,0.00023210915,0.0013184644,0.0008942475,0.0007375126,0.14987692],"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":[0.0005304595,0.000114671784,0.0064200056,0.0032100917,0.00008488234,0.00026124914,0.00009715135,0.0004113857,0.00028393668,0.00052537257,0.9749014,0.013159403],"study_design_scores_gemma":[0.007870201,0.00048042106,0.08547156,0.005613168,0.0003862059,0.0026519052,0.000742295,0.0036108305,0.002602889,0.013400353,0.8768632,0.00030700737],"about_ca_topic_score_codex":0.0076331566,"about_ca_topic_score_gemma":0.0146752,"teacher_disagreement_score":0.86614615,"about_ca_system_score_codex":0.00085079344,"about_ca_system_score_gemma":0.0013119908,"threshold_uncertainty_score":0.19092631},"labels":[],"label_agreement":null},{"id":"W6958175695","doi":"10.6084/m9.figshare.15153895.v1","title":"Additional file 4 of Childhood-onset dystonia-causing KMT2B variants result in a distinctive genomic hypermethylation profile","year":2021,"lang":"en","type":"article","venue":"Figshare","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":false,"ca_institutions":"London Health Sciences Centre; Western University","funders":"","keywords":"Selection (genetic algorithm); Genome; Cluster (spacecraft); Sample (material); genomic DNA; Genomics","score_opus":0.04194155674570194,"score_gpt":0.24819021338517697,"score_spread":0.20624865663947503,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W6958175695","genre_codex":"dataset","genre_gemma":"dataset","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"dataset","genre_consensus":"dataset","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.00047561343,0.00002702893,0.0005105744,0.000103126964,0.00003178966,0.00005898725,0.99757355,0.00058473094,0.0006345511],"genre_scores_gemma":[0.014542544,0.00014703319,0.0058305496,0.0006019909,0.00009187467,0.0012620371,0.9679002,0.001401859,0.008221934],"study_design_codex":"not_applicable","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99928135,0.00009750163,0.00011553941,0.00023412144,0.00016019931,0.00011123064],"domain_scores_gemma":[0.98440695,0.012201493,0.0007328751,0.001008977,0.0012546865,0.00039501349],"candidate_categories":["insufficient_payload"],"consensus_categories":[],"category_scores_codex":[0.0014385224,0.0012332974,0.001380592,0.0020192752,0.0011244403,0.0015335403,0.0019596554,0.0014079462,0.8367712],"category_scores_gemma":[0.02084108,0.00058570266,0.0010469711,0.0023068748,0.00030625885,0.0012386363,0.0009304331,0.0009368097,0.1266462],"study_design_candidate":"bench_or_experimental","study_design_consensus":null,"about_ca_topic_candidate":false,"about_ca_topic_consensus":false,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0008338876,0.00016761862,0.008020088,0.0038443792,0.00013377494,0.00039730512,0.00014951765,0.0007311896,0.0008726728,0.0005863927,0.9683092,0.015954033],"study_design_scores_gemma":[0.009535125,0.0006432852,0.09801222,0.004579886,0.00063208473,0.0031886136,0.00087833015,0.005103351,0.0059058596,0.014018219,0.85713446,0.00036855694],"about_ca_topic_score_codex":0.006874578,"about_ca_topic_score_gemma":0.014298618,"teacher_disagreement_score":0.8367712,"about_ca_system_score_codex":0.00089797575,"about_ca_system_score_gemma":0.0015507347,"threshold_uncertainty_score":0.23282611},"labels":[],"label_agreement":null},{"id":"W6976979320","doi":"10.6084/m9.figshare.21275690","title":"Additional file 1 of Evaluation of children with severe neurological impairment admitted to hospital with pain and irritability","year":2022,"lang":"en","type":"article","venue":"Figshare","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":false,"ca_institutions":"BC Children's Hospital; Children's Hospital of Eastern Ontario; University of British Columbia; University of Ottawa","funders":"","keywords":"Irritability; Medical diagnosis; Table (database); Hospital admission; Diagnosis code","score_opus":0.02493822708619312,"score_gpt":0.23212328284037742,"score_spread":0.2071850557541843,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W6976979320","genre_codex":"dataset","genre_gemma":"other","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"other","genre_consensus":null,"domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.000728345,0.000016533328,0.0000934179,0.00014014238,0.00001926218,0.00015467894,0.9958674,0.00005414632,0.00292613],"genre_scores_gemma":[0.019512787,0.00020941456,0.0012484513,0.0008409965,0.0001515627,0.0031391045,0.9575382,0.00022954638,0.017129907],"study_design_codex":"not_applicable","study_design_gemma":"not_applicable","domain_scores_codex":[0.9994456,0.00010308566,0.0001304072,0.00013685743,0.00008585017,0.00009807483],"domain_scores_gemma":[0.9910336,0.004678528,0.0015496834,0.0005348884,0.0017497543,0.00045356483],"candidate_categories":["insufficient_payload"],"consensus_categories":["insufficient_payload"],"category_scores_codex":[0.0006487527,0.0007298736,0.00078047195,0.0015578275,0.00096160674,0.0007302337,0.0009189405,0.00082514866,0.7544396],"category_scores_gemma":[0.014450861,0.00031980153,0.00047197472,0.0025311173,0.00013352056,0.0009741571,0.0007135607,0.0006615492,0.074619845],"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":[0.0003689057,0.00010201741,0.008349913,0.0008430543,0.000028224555,0.00013950976,0.000081508144,0.00016092797,0.000049272963,0.00047527527,0.98225766,0.007143827],"study_design_scores_gemma":[0.0055766082,0.0005292952,0.2119671,0.0074057267,0.0001920097,0.0018243608,0.0014144136,0.0016546691,0.0008707453,0.007836465,0.76055944,0.00016921187],"about_ca_topic_score_codex":0.014192592,"about_ca_topic_score_gemma":0.020792425,"teacher_disagreement_score":0.24556041,"about_ca_system_score_codex":0.0011610377,"about_ca_system_score_gemma":0.0014890204,"threshold_uncertainty_score":0.3502621},"labels":[],"label_agreement":null},{"id":"W6977172887","doi":"10.6084/m9.figshare.19418218.v1","title":"Additional file 1 of An integrated modelling methodology for estimating global incidence and prevalence of hereditary spastic paraplegia subtypes SPG4, SPG7, SPG11, and SPG15","year":2022,"lang":"en","type":"article","venue":"Figshare","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":false,"ca_institutions":"University of Toronto","funders":"","keywords":"Incidence (geometry); Hereditary spastic paraplegia; Paraplegia; Disease; MEDLINE","score_opus":0.13323537255511864,"score_gpt":0.31346618261400566,"score_spread":0.18023081005888703,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W6977172887","genre_codex":"dataset","genre_gemma":"dataset","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"dataset","genre_consensus":"dataset","domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.00075073866,0.000023576846,0.0048540514,0.00014229942,0.000020477277,0.0001037043,0.9918976,0.0006335089,0.001574],"genre_scores_gemma":[0.05317948,0.00020772233,0.039101012,0.00056651735,0.00009205377,0.0039529395,0.8850008,0.0021748766,0.01572448],"study_design_codex":"not_applicable","study_design_gemma":"simulation_or_modeling","domain_scores_codex":[0.999154,0.00036736787,0.00009394653,0.00021071872,0.0001059734,0.000068001085],"domain_scores_gemma":[0.9747863,0.022015732,0.00070573215,0.0010842305,0.0012283223,0.00017975832],"candidate_categories":["insufficient_payload"],"consensus_categories":[],"category_scores_codex":[0.003186996,0.0008132732,0.0007052567,0.0014473329,0.00044480697,0.0010685556,0.0016915664,0.0010950445,0.6561689],"category_scores_gemma":[0.034403775,0.00057627464,0.0012262833,0.0028355848,0.00019529315,0.00093151437,0.0007277012,0.0009899088,0.07926065],"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":[0.00030664238,0.00009733543,0.015352654,0.0013539196,0.00024402823,0.00012169539,0.00014847796,0.012173041,0.00011131936,0.0040053534,0.9449725,0.021112973],"study_design_scores_gemma":[0.0042856163,0.000478642,0.052944906,0.0026544563,0.0009454724,0.00089639233,0.00079480885,0.07011069,0.0012973753,0.04538363,0.8199854,0.00022262127],"about_ca_topic_score_codex":0.016284654,"about_ca_topic_score_gemma":0.01882443,"teacher_disagreement_score":0.6561689,"about_ca_system_score_codex":0.00089178584,"about_ca_system_score_gemma":0.0013816581,"threshold_uncertainty_score":0.49043334},"labels":[],"label_agreement":null},{"id":"W7023919064","doi":"","title":"Phenotypic differences between Peripheral Myelin Protein-22 (PMP-22) and Protein Zero (PO) mutations associated with Charcot-Marie-Tooth related diseases","year":2002,"lang":"en","type":"dissertation","venue":"eScholarship@McGill (McGill)","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":0,"is_retracted":false,"has_abstract":true,"route_ca_aff":false,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":true,"ca_institutions":"","funders":"Canadian Institutes of Health Research; Muscular Dystrophy Association","keywords":"Phenotype; Mutation; Myelin; Allele; Reproduction","score_opus":0.02390901486518892,"score_gpt":0.23090635897479808,"score_spread":0.20699734410960915,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W7023919064","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":[0.9886684,0.0007497282,0.00035248336,0.00032874278,0.00003973531,0.000017785176,0.00040618202,0.00001833807,0.009418615],"genre_scores_gemma":[0.96849895,0.00086939865,0.00068019197,0.00013287428,0.000021059823,0.000026048774,0.00036065085,0.000019432882,0.02939147],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9999207,0.000016264641,0.000007532181,0.00001831283,0.000020519767,0.000016722304],"domain_scores_gemma":[0.9998913,0.000032945216,0.000014994512,0.0000047483954,0.000014860424,0.000041072286],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00013837106,0.00023717534,0.00009810651,0.00037195304,0.00021593481,0.00026153246,0.00012882249,0.00023223733,0.0125506455],"category_scores_gemma":[0.00033068447,0.000082287224,0.00007842697,0.00012933832,0.00023195962,0.00008914245,0.00026405073,0.00015824629,0.00094007957],"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":[0.0012433175,0.00023497068,0.04048934,0.0002153701,0.0000521133,0.020501537,0.0017713216,0.00022606134,0.8645888,0.0021662973,0.006576622,0.061934207],"study_design_scores_gemma":[0.00019779305,0.0009821258,0.74326706,0.00016032395,0.00011762821,0.06514175,0.002256283,0.00068178924,0.1335869,0.0013747483,0.052189358,0.000044180382],"about_ca_topic_score_codex":0.0029316829,"about_ca_topic_score_gemma":0.004137442,"teacher_disagreement_score":0.0125506455,"about_ca_system_score_codex":0.00023563066,"about_ca_system_score_gemma":0.00017623641,"threshold_uncertainty_score":0.041986108},"labels":[],"label_agreement":null},{"id":"W7038212627","doi":"","title":"Genetic analysis of the hereditary spastic paraplegias","year":2006,"lang":"en","type":"dissertation","venue":"eScholarship@McGill (McGill)","topic":"Hereditary Neurological Disorders","field":"Neuroscience","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":"Hereditary spastic paraplegia; Locus (genetics); Disease gene identification; Missense mutation; Gene; Genetic analysis; Mutation; Candidate gene","score_opus":0.021606704111980374,"score_gpt":0.2409647494977448,"score_spread":0.21935804538576442,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W7038212627","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":[0.99506456,0.0003896964,0.0008225127,0.00013569667,0.000011453136,0.000042890017,0.0008311866,0.000045248165,0.0026568044],"genre_scores_gemma":[0.99617046,0.000489933,0.000805486,0.000092145805,0.000008177515,0.000011953775,0.00074271497,0.000013036875,0.0016660978],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9998665,0.0000174105,0.000010606328,0.000030811017,0.000049544004,0.00002506366],"domain_scores_gemma":[0.99988353,0.000027016566,0.00002424527,0.000005625811,0.000025712257,0.000033884782],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00012278928,0.0005097941,0.00020136288,0.0013380768,0.0004632807,0.00019303159,0.00016727734,0.00024841286,0.0017656746],"category_scores_gemma":[0.00029241559,0.00014770376,0.0003027326,0.000533818,0.00025931743,0.000054294545,0.00033433468,0.0002221669,0.0002118809],"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":[0.00057375646,0.00016013789,0.087669455,0.0002304873,0.00023322135,0.027346795,0.00069923786,0.00048871635,0.8572661,0.00072594837,0.0008778461,0.023728354],"study_design_scores_gemma":[0.00006760057,0.0006329856,0.8662407,0.00010848016,0.0004114866,0.038656343,0.000592069,0.0018011859,0.077716455,0.00035053445,0.01338367,0.000038455724],"about_ca_topic_score_codex":0.01905997,"about_ca_topic_score_gemma":0.02856339,"teacher_disagreement_score":0.01905997,"about_ca_system_score_codex":0.00054804236,"about_ca_system_score_gemma":0.0006218727,"threshold_uncertainty_score":0.037898004},"labels":[],"label_agreement":null},{"id":"W7039853336","doi":"","title":"Métallogénie du gîte à PB-ZN-AG Nicholas-Denys, Nouveau-Brunswick","year":2011,"lang":"fr","type":"other","venue":"","topic":"Hereditary Neurological Disorders","field":"Neuroscience","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":"Metamorphic petrology; Prospection; Telmatology","score_opus":0.029693334154764883,"score_gpt":0.23859176368004706,"score_spread":0.20889842952528218,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W7039853336","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":[0.93012565,0.003551049,0.0042064697,0.00056877115,0.000087432796,0.000110281464,0.002471375,0.00022914242,0.058649726],"genre_scores_gemma":[0.9154332,0.0019775417,0.0067992434,0.00011249243,0.000004603286,0.000047627567,0.0014371517,0.00007870721,0.07410932],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9998472,0.000008844651,0.0000067211713,0.00004482924,0.000051736402,0.000040776096],"domain_scores_gemma":[0.9999156,0.00001018682,0.00001100006,0.000006251844,0.000046147405,0.00001081636],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00020716188,0.00047859826,0.00017630952,0.00084466295,0.0007761114,0.0005624869,0.00040679038,0.00017158399,0.0037936373],"category_scores_gemma":[0.00026828633,0.0003197732,0.00015329671,0.0007657858,0.0004841139,0.00016982172,0.00040662155,0.000351636,0.000620229],"study_design_candidate":"observational","study_design_consensus":null,"about_ca_topic_candidate":true,"about_ca_topic_consensus":true,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.0007837849,0.00005510452,0.103682294,0.00069244776,0.00011558893,0.0027451296,0.0026072764,0.008151348,0.77188385,0.0084326845,0.005511745,0.095338784],"study_design_scores_gemma":[0.00010323383,0.00023612256,0.504135,0.00019431602,0.00007702424,0.0015140998,0.0026374243,0.0040279785,0.3037212,0.0013289758,0.18195459,0.00007003527],"about_ca_topic_score_codex":0.7460883,"about_ca_topic_score_gemma":0.88540417,"teacher_disagreement_score":0.25391167,"about_ca_system_score_codex":0.006630131,"about_ca_system_score_gemma":0.003379693,"threshold_uncertainty_score":0.51081395},"labels":[],"label_agreement":null},{"id":"W7088540732","doi":"10.5281/zenodo.17116222","title":"Processed and quality controlled surface fluxes and meteorological observations at Westham Island (CA-Wes)","year":2025,"lang":"en","type":"dataset","venue":"Zenodo (CERN European Organization for Nuclear Research)","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":"Western University; University of British Columbia","funders":"","keywords":"Eddy covariance; Flux (metallurgy); Sensible heat; Wind speed; Latent heat; Planetary boundary layer; Tower","score_opus":0.08837864760957044,"score_gpt":0.2946927608133657,"score_spread":0.20631411320379528,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W7088540732","genre_codex":"empirical","genre_gemma":"dataset","domain_codex":null,"domain_gemma":null,"model_version":"metacan-v3-hybrid-931329e0061c","genre_candidate":"dataset","genre_consensus":null,"domain_candidate":null,"domain_consensus":null,"prediction_status":"machine_predicted_unvalidated","genre_scores_codex":[0.52254254,0.00037531156,0.013838063,0.00041667707,0.00034617074,0.0008865321,0.37931255,0.0038415978,0.078440525],"genre_scores_gemma":[0.4891859,0.00040946255,0.066376075,0.00034439153,0.00014312589,0.0013954372,0.38674203,0.001998169,0.05340535],"study_design_codex":"not_applicable","study_design_gemma":"not_applicable","domain_scores_codex":[0.99941075,0.000025288728,0.000034350775,0.00018631479,0.0002763928,0.00006699481],"domain_scores_gemma":[0.99797875,0.00007627215,0.00012577572,0.00022282281,0.0014958768,0.0001005497],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0004754211,0.00050533324,0.00037602367,0.0008436385,0.00088769925,0.0009861469,0.0008221568,0.00036254807,0.009355091],"category_scores_gemma":[0.001448623,0.00026399837,0.00030293473,0.002081872,0.00023186917,0.0007974132,0.0004976089,0.00047215272,0.002616852],"study_design_candidate":"not_applicable","study_design_consensus":"not_applicable","about_ca_topic_candidate":true,"about_ca_topic_consensus":true,"about_ca_system_candidate":false,"about_ca_system_consensus":false,"study_design_scores_codex":[0.00094459724,0.0004694806,0.33887106,0.0008627477,0.00028905072,0.0007518362,0.0020440049,0.015136159,0.04439713,0.0027312087,0.43220535,0.16129741],"study_design_scores_gemma":[0.000099271194,0.00002745265,0.8076606,0.00010152111,0.00005696067,0.00005905691,0.0007184964,0.011992517,0.009504063,0.00023377963,0.16946723,0.00007901859],"about_ca_topic_score_codex":0.6401838,"about_ca_topic_score_gemma":0.77382016,"teacher_disagreement_score":0.3598162,"about_ca_system_score_codex":0.0017499054,"about_ca_system_score_gemma":0.0052729263,"threshold_uncertainty_score":0.7238704},"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":"W7120793899","doi":"","title":"Clinical and neurophysiologic evaluation of possible consequences of diabetes mellitus or glucose tolerance impairment in patients wiith hereditary motor and sensory neuropathy secondary to chromosome 17p11.2 duplication","year":2015,"lang":"pt","type":"dissertation","venue":"LA Referencia (Red Federada de Repositorios Institucionales de Publicaciones Científicas)","topic":"Hereditary Neurological Disorders","field":"Neuroscience","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":"Diabetes mellitus; Peripheral neuropathy; Sensory neuropathy; Diabetic neuropathy; Impaired glucose tolerance; Glucose tolerance test","score_opus":0.04023814170011124,"score_gpt":0.29461947452041376,"score_spread":0.2543813328203025,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W7120793899","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":[0.99773777,0.00051996537,0.000074162745,0.000041783675,0.000008197087,0.000032600394,0.00011756715,0.00000413909,0.0014638097],"genre_scores_gemma":[0.9988856,0.00037265246,0.00012425639,0.000057736448,0.000013110124,0.000020141306,0.00014665212,0.0000012546848,0.0003786474],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9998235,0.000035428344,0.000027566897,0.00003691125,0.000024611465,0.000052111365],"domain_scores_gemma":[0.999458,0.000116188734,0.00014311385,0.000019589823,0.00008124302,0.00018180879],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00028507292,0.00036478214,0.0004055448,0.0008948761,0.00041219036,0.0004685185,0.00019914325,0.000502495,0.0015848624],"category_scores_gemma":[0.0013478248,0.00015570091,0.00022633118,0.0005724961,0.0003534649,0.0003006823,0.00030723825,0.00034003038,0.00023452904],"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":[0.00080406625,0.00018871842,0.97896785,0.000065954715,0.000050139344,0.008732724,0.00029456307,0.000101731894,0.0032564967,0.000026607431,0.0001768251,0.007334381],"study_design_scores_gemma":[0.000032579417,0.001045506,0.98583174,0.000017850412,0.000034941444,0.011813164,0.00046871294,0.00015154702,0.00032815142,0.000040686034,0.00022488095,0.000010244306],"about_ca_topic_score_codex":0.0031397494,"about_ca_topic_score_gemma":0.003928094,"teacher_disagreement_score":0.0031397494,"about_ca_system_score_codex":0.00034240863,"about_ca_system_score_gemma":0.00038030106,"threshold_uncertainty_score":0.0062429905},"labels":[],"label_agreement":null},{"id":"W7127299708","doi":"10.36185/2532-1900-1593","title":"3-Methyl Glutaconic Aciduria and Elevated Plasma Growth Differentiation Factor 15 Level in an Adult with Monoallelic <i>SPG7</i> Pathogenic Variant.","year":2025,"lang":"en","type":"article","venue":"PubMed","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":false,"ca_institutions":"McMaster University","funders":"","keywords":"Mitochondrion; Disease; Growth factor; Gene; Pathogenesis; Heterozygote advantage","score_opus":0.031834676562430664,"score_gpt":0.22361849468219377,"score_spread":0.1917838181197631,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W7127299708","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":[0.9903016,0.0013900474,0.0007911293,0.0012916181,0.00012648005,0.000069030946,0.0004889825,0.00007389423,0.005467274],"genre_scores_gemma":[0.99857104,0.00022664326,0.00029263823,0.0002277659,0.000068596215,0.000006499383,0.00010783274,0.0000073875153,0.00049162324],"study_design_codex":"case_report","study_design_gemma":"case_report","domain_scores_codex":[0.9998029,0.000023613207,0.000027064827,0.00006552777,0.000032556247,0.00004839915],"domain_scores_gemma":[0.9996804,0.000069054186,0.00005461401,0.000015950995,0.000030577274,0.00014939664],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00017678509,0.0012434247,0.00046719506,0.0012579628,0.0009119318,0.000322478,0.0007231378,0.0024688905,0.002194026],"category_scores_gemma":[0.00091315387,0.00040342752,0.0004632346,0.0006886031,0.00095003954,0.0004929789,0.0003515269,0.0011158814,0.00032972524],"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":[0.0005422568,0.00012176118,0.052548952,0.000049492097,0.000055678745,0.93526334,0.00024042657,0.00017947593,0.0077828,0.00023129514,0.00066689885,0.002317658],"study_design_scores_gemma":[0.0000590894,0.0006765214,0.19160996,0.00004937128,0.00012138739,0.8028477,0.0003057607,0.0007997789,0.0021045632,0.0004827433,0.0009102623,0.000032801818],"about_ca_topic_score_codex":0.0064631067,"about_ca_topic_score_gemma":0.005367006,"teacher_disagreement_score":0.0064631067,"about_ca_system_score_codex":0.0005449966,"about_ca_system_score_gemma":0.0003844011,"threshold_uncertainty_score":0.012851},"labels":[],"label_agreement":null},{"id":"W7145786619","doi":"","title":"ALS5/SPG11/KIAA1840 mutations cause autosomal recessive axonal Charcot–Marie–Tooth disease","year":2015,"lang":"en","type":"article","venue":"Institutional Repositories DataBase (IRDB)","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":0,"is_retracted":false,"has_abstract":true,"route_ca_aff":false,"route_ca_fund":true,"route_ca_venue":false,"route_about_ca":true,"ca_institutions":"","funders":"Japan Society for the Promotion of Science; Ministero della Salute; Canada Excellence Research Chairs, Government of Canada; Brain Science Foundation","keywords":"Hereditary spastic paraplegia; Corpus callosum; Hereditary motor and sensory neuropathy; Autosomal recessive trait; Peripheral neuropathy; Disease; Disease gene identification; Degenerative disease; Myopathy","score_opus":0.07680027486375127,"score_gpt":0.3047305642275586,"score_spread":0.22793028936380735,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W7145786619","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":[0.9987062,0.0002523195,0.00026046953,0.000015082722,0.0000039963707,0.000018219731,0.00013536598,0.000012884263,0.0005954197],"genre_scores_gemma":[0.99878055,0.00017361027,0.00033935462,0.000043302014,0.0000052377427,0.000009042597,0.00025812676,0.0000062804625,0.00038442755],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9997466,0.00002664037,0.000030059655,0.00007015537,0.000079093545,0.000047415884],"domain_scores_gemma":[0.99980885,0.00004639288,0.00005053445,0.000011057478,0.000020593217,0.000062511965],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00016181852,0.0009119426,0.0002897075,0.0008852522,0.0005447917,0.00023764909,0.00025670376,0.0005212071,0.001692367],"category_scores_gemma":[0.00045521956,0.00026215857,0.00029592242,0.00056861195,0.00044023365,0.00013530412,0.00058193883,0.00028022967,0.00043466093],"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":[0.0008479548,0.00035729678,0.32491797,0.00027761888,0.0003047954,0.15847139,0.002146903,0.00069667696,0.4903421,0.00034040737,0.0008020607,0.020494774],"study_design_scores_gemma":[0.00011377741,0.00071077864,0.86320055,0.00004340088,0.00016961063,0.10034055,0.00069278653,0.00072251726,0.02956191,0.00021235221,0.0041906955,0.00004110477],"about_ca_topic_score_codex":0.002783084,"about_ca_topic_score_gemma":0.0027125839,"teacher_disagreement_score":0.002783084,"about_ca_system_score_codex":0.0002812178,"about_ca_system_score_gemma":0.0001621353,"threshold_uncertainty_score":0.0056614876},"labels":[],"label_agreement":null},{"id":"W7146564911","doi":"","title":"Hereditary spastic paraplegia : a novel mutation and expansion of the phenotype variability in SPG10","year":2014,"lang":"en","type":"article","venue":"Institutional Repositories DataBase (IRDB)","topic":"Hereditary Neurological Disorders","field":"Neuroscience","cited_by":0,"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":"Canada Excellence Research Chairs, Government of Canada","keywords":"Hereditary spastic paraplegia; Spasticity; Genetic heterogeneity; Spastic; Mutation; Peripheral neuropathy; Neurology; Neurological disorder; Paraplegia","score_opus":0.022881669180246193,"score_gpt":0.24564196033077385,"score_spread":0.22276029115052765,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W7146564911","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":[0.99453825,0.00032358375,0.0013832038,0.0002214078,0.00005534187,0.00011028382,0.00059734145,0.00009159047,0.002678894],"genre_scores_gemma":[0.99781406,0.00012551883,0.0008238908,0.000111571375,0.00005413319,0.000028834302,0.00031877102,0.000021686124,0.0007015093],"study_design_codex":"case_report","study_design_gemma":"case_report","domain_scores_codex":[0.9996749,0.00006069119,0.00003484175,0.000121684934,0.000056371682,0.00005151649],"domain_scores_gemma":[0.99947256,0.00019791366,0.000117437114,0.00003894851,0.000041867024,0.00013130475],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00024303395,0.0020333882,0.0005063878,0.001355032,0.00050676055,0.00035083623,0.0006283901,0.0012610249,0.0050610215],"category_scores_gemma":[0.0010684798,0.00029594186,0.00083767605,0.0007018419,0.00092914765,0.0001550721,0.0007636124,0.00054141704,0.0009009869],"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":[0.0010070135,0.0004086154,0.0990806,0.00024071758,0.00022053366,0.7262477,0.0013983918,0.00042277196,0.15142947,0.0008136345,0.001339843,0.017390642],"study_design_scores_gemma":[0.00017830342,0.00086594955,0.27140918,0.00012500462,0.00017705746,0.70965964,0.00042154745,0.0012795348,0.009632193,0.0004291537,0.0057577,0.000064695145],"about_ca_topic_score_codex":0.0018699017,"about_ca_topic_score_gemma":0.0018947708,"teacher_disagreement_score":0.0050610215,"about_ca_system_score_codex":0.00037167303,"about_ca_system_score_gemma":0.00036897918,"threshold_uncertainty_score":0.016930819},"labels":[],"label_agreement":null},{"id":"W7161937866","doi":"10.82308/24364","title":"Genetics of hereditary spastic paraplegia","year":2021,"lang":"en","type":"dissertation","venue":"","topic":"Hereditary Neurological Disorders","field":"Neuroscience","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":"Hereditary spastic paraplegia; Genetic heterogeneity; Sanger sequencing; Exome sequencing; Spasticity; Gene; Genetic counseling; Genetic testing; Spastic","score_opus":0.035177515200543436,"score_gpt":0.28187859234295914,"score_spread":0.2467010771424157,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W7161937866","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":[0.98153424,0.005221065,0.0020782782,0.0010330131,0.000038369963,0.00008318541,0.0006849916,0.00008347325,0.009243401],"genre_scores_gemma":[0.9956359,0.0018450496,0.00097525044,0.00017081983,0.000052935127,0.000016253476,0.00043368965,0.000009053284,0.0008609507],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9996792,0.000054860913,0.000025663674,0.000064974956,0.00010666604,0.00006871165],"domain_scores_gemma":[0.9996439,0.00009100653,0.00010444812,0.000011881092,0.00008129069,0.00006747666],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00024732106,0.0009768398,0.00031009744,0.0015182688,0.0007076838,0.00036577164,0.00045861158,0.00048522727,0.002797674],"category_scores_gemma":[0.0006071505,0.00016447126,0.00024165591,0.0015400499,0.0010022498,0.00018307466,0.0005278468,0.00029113513,0.00021176216],"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":[0.00066141976,0.00018474404,0.7912623,0.00070861686,0.00042721417,0.09784022,0.0019609951,0.002804686,0.043072864,0.0077480716,0.0050467746,0.04828205],"study_design_scores_gemma":[0.00008985203,0.00036335943,0.82635117,0.00030888422,0.00047754226,0.14732938,0.0008952192,0.0019850533,0.0057226783,0.0043797945,0.012049197,0.000047840764],"about_ca_topic_score_codex":0.03669105,"about_ca_topic_score_gemma":0.030991044,"teacher_disagreement_score":0.03669105,"about_ca_system_score_codex":0.0017292557,"about_ca_system_score_gemma":0.0027096393,"threshold_uncertainty_score":0.07295495},"labels":[],"label_agreement":null},{"id":"W7161959930","doi":"10.82308/28286","title":"Genetic analysis of the hereditary spastic paraplegias","year":2006,"lang":"en","type":"dissertation","venue":"","topic":"Hereditary Neurological Disorders","field":"Neuroscience","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":"Hereditary spastic paraplegia; Locus (genetics); Disease gene identification; Missense mutation; Gene; Genetic analysis; Mutation; Candidate gene","score_opus":0.020500177241104936,"score_gpt":0.256392097414602,"score_spread":0.23589192017349708,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W7161959930","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":[0.99506456,0.0003896964,0.0008225127,0.00013569667,0.000011453136,0.000042890017,0.0008311866,0.000045248165,0.0026568044],"genre_scores_gemma":[0.99617046,0.000489933,0.000805486,0.000092145805,0.000008177515,0.000011953775,0.00074271497,0.000013036875,0.0016660978],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9998665,0.0000174105,0.000010606328,0.000030811017,0.000049544004,0.00002506366],"domain_scores_gemma":[0.99988353,0.000027016566,0.00002424527,0.000005625811,0.000025712257,0.000033884782],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00012278928,0.0005097941,0.00020136288,0.0013380768,0.0004632807,0.00019303159,0.00016727734,0.00024841286,0.0017656746],"category_scores_gemma":[0.00029241559,0.00014770376,0.0003027326,0.000533818,0.00025931743,0.000054294545,0.00033433468,0.0002221669,0.0002118809],"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":[0.00057375646,0.00016013789,0.087669455,0.0002304873,0.00023322135,0.027346795,0.00069923786,0.00048871635,0.8572661,0.00072594837,0.0008778461,0.023728354],"study_design_scores_gemma":[0.00006760057,0.0006329856,0.8662407,0.00010848016,0.0004114866,0.038656343,0.000592069,0.0018011859,0.077716455,0.00035053445,0.01338367,0.000038455724],"about_ca_topic_score_codex":0.01905997,"about_ca_topic_score_gemma":0.02856339,"teacher_disagreement_score":0.01905997,"about_ca_system_score_codex":0.00054804236,"about_ca_system_score_gemma":0.0006218727,"threshold_uncertainty_score":0.037898004},"labels":[],"label_agreement":null},{"id":"W7161961472","doi":"10.82308/28758","title":"The genetics of hereditary spastic paraplegia","year":2022,"lang":"en","type":"dissertation","venue":"","topic":"Hereditary Neurological Disorders","field":"Neuroscience","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":"Genetic inheritance; Hereditary spastic paraplegia; Animal model","score_opus":0.028411134091790646,"score_gpt":0.2837192310366298,"score_spread":0.2553080969448392,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W7161961472","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":[0.945552,0.031864066,0.0018416692,0.007724004,0.00008776523,0.000048866084,0.0012367577,0.00005389884,0.011590918],"genre_scores_gemma":[0.9816289,0.014027919,0.00093623146,0.00050557556,0.00009442158,0.000013939433,0.00024197962,0.000006224732,0.002544674],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9997197,0.00005151344,0.000026597665,0.00006144086,0.0000823557,0.000058408736],"domain_scores_gemma":[0.9994947,0.00017101136,0.00012496565,0.000017310402,0.00013170547,0.000060366827],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0003164695,0.00034798184,0.0002614133,0.0008062449,0.0006879826,0.000776955,0.00037068702,0.00057991897,0.002810244],"category_scores_gemma":[0.0014784054,0.000120935634,0.00012318484,0.001200926,0.0019206309,0.00026529783,0.0005812326,0.00032331378,0.00014417488],"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":[0.00043041861,0.00011526515,0.8277605,0.001537096,0.00034267854,0.015393102,0.004142522,0.0026807915,0.022249907,0.020268403,0.0049422034,0.1001371],"study_design_scores_gemma":[0.000065097964,0.00028316854,0.8987522,0.0010296939,0.00049190543,0.05020198,0.004134981,0.0012937913,0.0044220304,0.010100316,0.02917767,0.000047202902],"about_ca_topic_score_codex":0.24254076,"about_ca_topic_score_gemma":0.22871207,"teacher_disagreement_score":0.24254076,"about_ca_system_score_codex":0.0030694385,"about_ca_system_score_gemma":0.0072366027,"threshold_uncertainty_score":0.48225808},"labels":[],"label_agreement":null},{"id":"W7161967467","doi":"10.82308/4309","title":"Expression and proteomic analysis of KlFlA/25B in hereditary sensory and autonomic neuropathies type ll","year":2017,"lang":"en","type":"dissertation","venue":"","topic":"Hereditary Neurological Disorders","field":"Neuroscience","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":"Exon; Gene isoform; Alternative splicing; Gene; Disease; Identification (biology); Mutation; RNA splicing","score_opus":0.03180362346430229,"score_gpt":0.2856275616572351,"score_spread":0.2538239381929328,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W7161967467","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":[0.9934278,0.0025524346,0.0008100511,0.00009793344,0.000044638637,0.000016594988,0.0019813054,0.00004961,0.0010194953],"genre_scores_gemma":[0.9869164,0.0016659009,0.0028569053,0.00021304486,0.000022929808,0.000036888425,0.003795375,0.000036155903,0.004456329],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.99991333,0.0000064221776,0.000008778167,0.000025754205,0.000024435223,0.000021201124],"domain_scores_gemma":[0.9999019,0.000012214484,0.000021708302,0.0000056572967,0.000023972363,0.000034572095],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0001367883,0.00028766668,0.00025661296,0.0009541988,0.00027776946,0.00031177292,0.00015819936,0.00029970406,0.0015637944],"category_scores_gemma":[0.00016189476,0.00013101105,0.00040248694,0.00038320757,0.00017085322,0.00013248947,0.00018969932,0.00020401379,0.00077726005],"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":[0.00062255113,0.00005890888,0.016098168,0.00018155736,0.00008346419,0.0018101278,0.00019224218,0.000080719714,0.976273,0.0000664972,0.00041182642,0.004121005],"study_design_scores_gemma":[0.000058316084,0.00067169906,0.7467361,0.00013670401,0.00023813131,0.009945837,0.0016940031,0.00278039,0.2213533,0.00017772218,0.016154744,0.00005303489],"about_ca_topic_score_codex":0.0018962186,"about_ca_topic_score_gemma":0.0021483337,"teacher_disagreement_score":0.0018962186,"about_ca_system_score_codex":0.00025835843,"about_ca_system_score_gemma":0.000103123464,"threshold_uncertainty_score":0.0052313805},"labels":[],"label_agreement":null},{"id":"W7162069996","doi":"10.82308/53363","title":"Genome-wide approaches to investigate rare neurological disorders in French Canadians","year":2018,"lang":"en","type":"dissertation","venue":"","topic":"Hereditary Neurological Disorders","field":"Neuroscience","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":"Medical screening; Population; Neurogenetics; Ile de france","score_opus":0.07848721256978586,"score_gpt":0.24211033921557998,"score_spread":0.16362312664579412,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W7162069996","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":[0.9185106,0.015206435,0.0070891683,0.0037343688,0.00018680748,0.00061373314,0.03471075,0.0002252209,0.019722931],"genre_scores_gemma":[0.9697399,0.0039238054,0.008464369,0.0012010502,0.000050212802,0.00039746187,0.008497839,0.00006612129,0.0076592877],"study_design_codex":"observational","study_design_gemma":"observational","domain_scores_codex":[0.9981679,0.00031068508,0.0000927257,0.0005060281,0.00040541615,0.00051732804],"domain_scores_gemma":[0.99782324,0.00034944524,0.00020529801,0.000114671435,0.0012294643,0.00027789216],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0022694967,0.00065326,0.0006508243,0.004263588,0.0037651134,0.0015023779,0.0011469824,0.000769069,0.004342807],"category_scores_gemma":[0.0045123235,0.0003050655,0.0012262535,0.007184983,0.0006121522,0.00022748063,0.0009440235,0.0005975503,0.00037542768],"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":[0.00052744115,0.000085538864,0.9212189,0.00038275804,0.0014145534,0.0009850737,0.0034858577,0.0015954261,0.004752454,0.0020345843,0.011601261,0.051916152],"study_design_scores_gemma":[0.00004283586,0.000055242726,0.9768529,0.000091713795,0.00035772257,0.00030276162,0.0018280618,0.0007243444,0.00036531518,0.00021859449,0.019130113,0.000030375402],"about_ca_topic_score_codex":0.9817203,"about_ca_topic_score_gemma":0.9887361,"teacher_disagreement_score":0.018279672,"about_ca_system_score_codex":0.01714176,"about_ca_system_score_gemma":0.023138447,"threshold_uncertainty_score":0.12437278},"labels":[],"label_agreement":null},{"id":"W7162129312","doi":"10.82308/47981","title":"Validation of KIF1A/25B interactors in hereditary sensory and autonomic neuropathies type II","year":2022,"lang":"en","type":"dissertation","venue":"","topic":"Hereditary Neurological Disorders","field":"Neuroscience","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":"Sensation; Population; Hereditary motor and sensory neuropathy; Arterial disease","score_opus":0.029440133515257656,"score_gpt":0.28115384179031144,"score_spread":0.2517137082750538,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W7162129312","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":[0.99488777,0.0014918682,0.0009433849,0.00005606109,0.000025047551,0.000054185686,0.0014210278,0.0000590374,0.0010617479],"genre_scores_gemma":[0.9943514,0.00043114618,0.001486137,0.000078194586,0.000009945309,0.00013117665,0.0018723332,0.000026107688,0.0016134535],"study_design_codex":"bench_or_experimental","study_design_gemma":"bench_or_experimental","domain_scores_codex":[0.9996381,0.00006955966,0.000030495345,0.000095471114,0.00008952214,0.000076911856],"domain_scores_gemma":[0.99968076,0.00009253137,0.0000491287,0.000038980404,0.00005194739,0.00008674813],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.00059264724,0.00052429765,0.00037417817,0.0012960309,0.00062000856,0.0005017541,0.0005219981,0.00046387262,0.0039290627],"category_scores_gemma":[0.00073454774,0.00023056762,0.00038300964,0.00048381608,0.00029950181,0.00016208862,0.00035929724,0.00031044974,0.0008302721],"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":[0.0030743775,0.00041154018,0.10042936,0.00022257783,0.00026990828,0.0013974037,0.000243973,0.0006588515,0.88134795,0.0001959167,0.0004838813,0.011264282],"study_design_scores_gemma":[0.00031955776,0.0033753014,0.671629,0.00009737936,0.00057674095,0.0049588713,0.00074981764,0.0053053387,0.29664782,0.00030831792,0.015977658,0.00005421585],"about_ca_topic_score_codex":0.005042067,"about_ca_topic_score_gemma":0.002371101,"teacher_disagreement_score":0.005042067,"about_ca_system_score_codex":0.00034007707,"about_ca_system_score_gemma":0.00022812681,"threshold_uncertainty_score":0.013143957},"labels":[],"label_agreement":null},{"id":"W7163426638","doi":"10.26262/heal.auth.ir.373494","title":"Μελέτη συσχέτισης της της μονονουκλεοτιδικής παραλλαγής rs5177 του γονιδίου LRP8 με την ανταπόκριση στη φαρμακοθεραπεία ασθενών με σχιζοφρένεια και άλλες ψυχωσικές διαταραχές","year":2025,"lang":"el","type":"article","venue":"Aristotle University of Thessaloniki","topic":"Hereditary Neurological Disorders","field":"Neuroscience","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":"LDL receptor; Lipoprotein; Receptor; Lipoprotein lipase; Lipoprotein(a)","score_opus":0.011489264351791347,"score_gpt":0.20861048638288807,"score_spread":0.19712122203109672,"validation_status":"score_only:v0-immature-baseline","prediction":{"id":"W7163426638","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":[0.5219517,0.019749995,0.10022981,0.016006056,0.0059827324,0.0004929077,0.031782568,0.007965163,0.2958392],"genre_scores_gemma":[0.8063005,0.005667295,0.02249209,0.0027470833,0.0005082007,0.0007504849,0.012987019,0.0018132513,0.14673418],"study_design_codex":"bench_or_experimental","study_design_gemma":"observational","domain_scores_codex":[0.9979164,0.00024472753,0.00008311037,0.0006918959,0.0007450637,0.00031879608],"domain_scores_gemma":[0.9985734,0.00043621875,0.00022600127,0.00028702288,0.00031374983,0.00016351684],"candidate_categories":[],"consensus_categories":[],"category_scores_codex":[0.0011710805,0.0009312557,0.00077365956,0.001255026,0.0014214863,0.0022929814,0.0012007242,0.0021556355,0.03379631],"category_scores_gemma":[0.0038215746,0.00056832476,0.0008300316,0.0010046738,0.0015004284,0.0018187603,0.0015759262,0.0023881714,0.016630154],"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":[0.0024544692,0.00018092105,0.01482603,0.0026026187,0.00041169056,0.002548739,0.0045505175,0.0022260016,0.71680224,0.03710134,0.05344259,0.16285291],"study_design_scores_gemma":[0.00016713857,0.0002817701,0.039235957,0.0005642423,0.00036337817,0.0020911866,0.0036962982,0.00092886295,0.21413629,0.021611597,0.7167068,0.00021646835],"about_ca_topic_score_codex":0.0057030516,"about_ca_topic_score_gemma":0.0033204562,"teacher_disagreement_score":0.03379631,"about_ca_system_score_codex":0.0014284198,"about_ca_system_score_gemma":0.0012761076,"threshold_uncertainty_score":0.11305994},"labels":[],"label_agreement":null}]}